Procedural Standards For Certified Testing of Cleanrooms

PROCEDURAL
STANDARDS FOR
CERTIFIED
TESTING OF
CLEANROOMS
2009 THIRD EDITION
National Environmental
Balancing Bureau
8575 Grovemont Circle
Gaithersburg, Maryland 20877
301-977-3698
301-977-9589 FAX
www.nebb.org
PROCEDURAL STANDARDS FOR CERTIFIED

TESTING OF CLEANROOMS
Copyright NEBB, 2009

FIRST EDITION OCTOBER 1988
SECOND EDITION APRIL 1996
THIRD EDITION OCTOBER 2009
This book may not be reproduced in any form without written permission of the copyright
owner.
These Procedural Standards were developed using reliable engineering principles and research plus
consultation with, and information obtained from, manufacturers, users, testing laboratories and others
having specialized experience. They are subject to revision as further experience and investigation may
show is necessary or desirable. Cleanroom Performance Testing, which complies with these
Procedural Standards, will not necessarily be acceptable, if when examined and tested, it is found to
have other features that impair the result intended by these standards. The National Environmental
Balancing Bureau assumes no responsibility and has no liability for the application of the principles or
techniques contained in these Procedural Standards. Authorities considering adoption of these
Procedural Standards should review all Federal, State, local and contract regulations applicable to the
specific installation.
II
FOREWORD
The purpose of the NEBB Procedural Standards for Certified Testing of Cleanrooms is to establish a
uniform and systematic set of criteria for the performance of cleanroom testing and certification.
Todays buildings provide highly controlled indoor environments. This is especially true when dealing
with clean environmental conditions required by todays micro-electronics, bio-medical, and other
highly technical industries. These conditions could not exist without sophisticated mechanical
systems created by a team of skilled professionals. A key member of this team is the NEBB Certified
Cleanroom Performance Testing (CPT) Firm.
This Third Edition represents a departure from past editions. All of the material devoted to Cleanroom
Fundamentals, contamination theory and practice, and various testing application data has been
intentionally omitted from this edition for two reasons. First, all of this material currently exists in the
NEBB Cleanroom Home Study Course and secondly, that type of material is not normally presented
in a published standard. This Procedural Standard presents the functional requirements of the NEBB
Cleanroom program and the testing and reporting requirements only. This edition is divided into two
distinct Parts: Standards and Procedures. These CPT procedural standards have been developed
using language defined by Shall, Should, and May as it relates to the standards and procedures
described in this manual. It is important to note these particular words throughout this manual and
how they pertain to the NEBB standards and procedures.
These standards and procedures are intended as the minimum NEBB requirements that a NEBB
Certified CPT Firm shall follow when performing Cleanroom Testing and Certification procedures.
Contract document requirements or contractual agreements between the Owner and the NEBB
Certified CPT Firm may supersede the NEBB requirements. These Procedural Standards have been
carefully compiled and reviewed by the NEBB Technical Committees.
Part 1 STANDARDS
Part 1, STANDARDS, covers the requirements for Quality Control and Compliance, Instrumentation
Requirements, and CPT Reports. Revised requirements for CPT instruments and reports are
identified. The new report requirements allow the NEBB Certified CPT Firm more flexibility in
designing their reports by prescribing sets of information that "Shall, Should and/or May" be required
to complete a CPT Report.
Part 2 PROCEDURES
Part 2, PROCEDURES, covers measurement procedures of the various testing requirements for
cleanroom testing and certification.
APPENDICES
The Appendices include a suggested CPT Specification, References, and Engineering Equations.
This Third Edition of the CPT Procedural Standards, when used by NEBB Certified CPT Firms, will
assure the building owner or operator that facility systems have been properly tested within design
and installation limitations.
Andrew P. Nolfo, PE
NEBB Technical Director
III
CLEANROOM COMMITTEE MEMBERS

AND OTHER CONTRIBUTORS FOR CURRENT AND
PREVIOUS EDITIONS
Current Cleanroom
Past Contributors:
Committee
Randall J. Silva Chairman
Robert Cherrington
San Jose, California
West Valley City, Utah
William C. Neudorfer, P.E.
Ken Goldstein
Seattle, Washington
Phoenix, Arizona
Donald E. Hill
Jerry Greiner
Independence, Missouri
Portland, Oregon
Patrick C. Law
Al Lieberman*
Altamonte Springs, Florida
Fremont, California
Dan Milholland
Wendell Lough
Raleigh, North Carolina
Hampstead, New Hampshire
W. David Bevirt, P.E
Kevin McCann
Tucson, Arizona
Ajax, Ontario, Canada
Andrew P. Nolfo, P.E
Phoenix, Arizona
Additional Contributors to the Third Edition:
Mike Dolim
Gaithersburg, Maryland
Lonnie Mosley
Spring Valley, California
Buff Ohnhaus
Albuquerque, New Mexico
Keith Reals
Baltimore. Maryland
Gary Rolf
Phoenix, Arizona
Robert Solana
Hauppauge, New York
Michael A. Weider
Bethlehem, Pennsylvania
* DECEASED
IV
TABLE OF CONTENTS
PAGE
Foreword
NEBB Cleanroom Committee
Table of Contents
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PART 1 STANDARDS
SECTION 1 Definitions
SECTION 2 NEBB Program, Quality Control and Compliance

2.1
2.2
2.3
2.4
NEBB Programs
2.1.1 NEBB Disciplines
2.1.2 Certification of Firms
2.1.3 Certification of Professionals
2.1.4 Certification of Technicians
2.1.5 Recertification Requirements
Quality Assurance Program Conformance Certification
2.2.1 Program Advantages
2.2.2 NEBB Quality Assurance Program Certificate
Quality Control and Compliance
2.3.1 Cleanroom Work Compliance
Certified CPT Professional Responsibilities
2.4.1 Execution of CPT Procedures
2.4.2 Technician Training
2.4.3 Cleanroom Procedures Training
2.4.4 Instrument Use and Maintenance
2.4.5 Coordination / Supervision
2.4.6 Project Communication
2.4.7 Field Work Completion
2.4.8 Compilation and Submission of Final Cleanroom Reports
2.4.9 Project Completion
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SECTION 3 Responsibilities
3.1
3.2
Introduction
Owner/Buyer and Design and Construction Team Responsibilities
3.2.1 Owner/Buyer and Design Professional Responsibilities
3.2.2 Owner/Buyer and/or Construction Team Responsibilities
3.2.3 NEBB Certified CPT Firm Responsibilities
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SECTION 4 Standards for Equipment, Instrumentation

and Calibration
4.1
4.2
Minimum Instrumentation
Range and Accuracy Use
Table 4-1 NEBB Minimum Instrumentation Requirements
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NEBB CPT PROCEDURAL STANDARDS
TABLE OF CONTENTS
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Table 4-2 NEBB Minimum (should) Instrumentation Requirements
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SECTION 5 Standards for Reports and Forms

5.1
5.2
5.3
5.4
5.5
5.6
5.7
5.8
5.9
5.10
5.11
5.12
5.13
5.14
5.15
5.16
5.17
5.18
5.19
5.20
5.21
5.22
5.23
5.24
5.25
5.26
Reports
Required Forms
5.2.1 Report Title
5.2.2 Report Certification
5.2.3 Table of Contents
5.2.4 Standard Operating Procedures (SOPs) References
5.2.5 Report Summary / Remarks
5.2.6 Instrument Calibration Certificates
5.2.7 Abbreviations
Airflow Velocity and Uniformity Test Filter Face Airflow Velocity
- Unidirectional
- Non-Unidirectional (Volume Method)
- Non-Unidirectional (Velocity Method)
Airflow Velocity and Uniformity Test Average Room Airflow
Velocity
Airflow Volume and Uniformity Test Flowhood Method
Airflow Volume and Uniformity Test Traverse Method
Filter Installation Leak Tests Aerosol Photometer
Test Method
Filter Installation Leak Tests Discrete Particle Counter
Test Method
Filter Installation Leak Tests Total Aerosol Penetration
Test Method
Airborne Particle Count Cleanliness Classification Tests
ISO Standard
Airborne Particle Counting Tests Sequential Sampling
Room Pressurization Tests
Airflow Parallelism Tests
Recovery Tests
Lighting Level and Uniformity Tests
Sound Level Tests
Vibration Level Tests
General Temperature and Humidity Uniformity Tests
Comprehensive Temperature and Humidity Uniformity Tests
Electrostatic Tests
Conductivity Tests
Electromagnetic Interference (EMI) Tests
Air Change Rate (ACH) Test
Bench Scan Filter Leak Tests
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PART 2 - PROCEDURES
SECTION 6 Cleanroom Standard Operating Procedures
6.1 Introduction
6.2 Standard Operating Procedures
6.2.1 Description
6.2.2 Format
6.2.3 Title
6.2.4 Purpose
6.2.5 Scope
6.2.6 Responsibility
6.2.7 References and Documents
6.2.8 Safety
6.2.9 Procedural Principles
6.2.10 Preliminary Operations
6.2.11 Procedures
6.2.12 Tools
6.2.13 Calculations
6.2.14 Documentation Requirements
6.3 Additional SOP Requirements
6.3.1 Language and Detail
6.3.2 Review and Approval
6.3.3 Distribution and Control
6.3.4 Modifications
6.3.5 Data Collection Forms / Reports
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SECTION 7 Cleanroom Safety

7.1 Introduction
7.2 Designing a Health and Safety Program
7.2.1 Designing a Program Policy
7.2.2 Designing a Training Program
7.2.3 Essentials of the Health and Safety Program
7.3 Responsibilities
7.3.1 Individual Health and Safety Responsibilities
7.3.2 NEBB Certified CPT Professional Responsibilities
7.3.3 Field Technician Responsibilities
7.4 Elements of the Program
7.4.1 Project Specific Items
7.4.2 Health and Safety Program Implementation
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SECTION 8 Cleanroom Protocol

8.1 Introduction
8.2 Cleanroom Procedures
8.2.1 Gowning Procedures
8.2.2 Equipment Entrance Procedures
8.2.3 Cleanroom Conduct
VII
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SECTION 9 Cleanroom Tests
9.1 Introduction
9.2 Cleanroom Airflows
9.2.1 Unidirectional Airflows
9.2.2 Non-unidirectional Airflows
9.2.3 Mixed Airflows
9.3 Occupancy Modes
9.3.1 As-Built Facility
9.3.2 At-Rest Facility
9.3.3 Operational Facility
9.3.4 Exceptions
9.4 Cleanliness Levels
9.5 Primary Tests
9.6 Secondary Tests
9.7 Testing Intervals
Table 9-1 Recommended Test by Cleanroom Type
Table 9-2 Recommended Testing Intervals
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SECTION 10 Primary Tests

10.1 Introduction
10.2 Cleanroom / Filter Airflow Velocity and Uniformity Tests
10.3 Airflow Velocity and Uniformity Test Filter Face Velocity
- Unidirectional
10.3.1 Instrumentation and Equipment
10.3.2 Test Procedures
10.3.3 Acceptance
10.3.4 Reporting
10.4 Airflow Velocity and Uniformity Test Filter Face Airflow Velocity
- Non-Unidirectional (Volume Method)
10.4.3 Acceptance
10.4.4 Reporting
10.5 Airflow Velocity and Uniformity Test Filter Face Airflow Velocity
- Non-Unidirectional (Velocity Method)
10.5.3 Acceptance
10.5.4 Reporting
10.6 Airflow Velocity and Uniformity Test Average Room Airflow
Velocity
10.6.3 Acceptance
10.6.4 Reporting
10.7 Airflow Volume and Uniformity Test
10.8 Airflow Volume and Uniformity Test Flowhood Method
VIII
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10.8.3 Acceptance
10.8.4 Reporting
10.9 Airflow Volume and Uniformity Test Traverse Method
10.9.3 Acceptance
10.9.4 Reporting
10.10 Filter Installation Leak Tests
10.10.1 Leak Test Methods
10.11 HEPA Filter Installation Leak Tests Aerosol Photometer
Test Method
10.11.3 Acceptance
10.11.4 Reporting
10.11.5 Repairs
10.12 HEPA Filter Installation Leak Tests Discrete Particle Counter
Test Method
10.12.3 Acceptance
10.12.4 Reporting
10.12.5 Repairs
10.13 HEPA Filter Installation Leak Tests Total Aerosol Penetration
Test Method
10.13.3 Acceptance
10.13.4 Reporting
10.13.5 Repairs
10.14 Airborne Particle Count Cleanliness Test ISO Standard 14644
10.14.3 Acceptance
10.14.4 Reporting
10.15 Airborne Particle Counting Tests Sequential Sampling
10.16 Room Pressurization Tests
10.16.3 Acceptance
10.16.4 Reporting
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SECTION 11 Secondary Tests

11.1 Introduction
11.2 Airflow Parallelism Tests
11.2.3 Acceptance
11.2.4 Reporting
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11.3 Recovery Tests Standard Method
11.3.3 Acceptance
11.3.4 Reporting
11.4 Lighting Level and Uniformity Tests
11.4.2 Test Procedures General (Applies to All Tests)
11.4.3 Test Procedures Determine of Average Luminance from
General Lighting
11.4.4 Test Procedures Symmetrically Spaced Luminaries in Two
or More Rows
11.4.5 Test Procedures Symmetrically Located Single Luminare
11.4.6 Test Procedures Individual Luminaires in Single Row
11.4.7 Test Procedures Two or More Continuous Rows of Luminares
11.4.8 Test Procedures Continuous Luminaires in a Single Row
11.4.9 Test Procedures Luminous or Louver-All Ceiling
11.4.10 Test Procedures Point of Work Measurements
11.4.11 Acceptance
11.4.12 Reporting
11.5 Sound Level Tests
11.5.2 Preliminary Test Procedures
11.5.4 Acceptance
11.5.5 Reporting
11.6 Vibration Level Tests
11.6.2 Preliminary Test Procedures
11.6.4 Acceptance
11.6.5 Reporting
11.7 Temperature and Humidity Uniformity Tests
11.8 General Temperature and Humidity Uniformity Tests
11.8.2 Test Procedures Temperature
11.8.3 Test Procedures Humidity
11.8.4 Acceptance
11.8.5 Reporting
11.9 Comprehensive Temperature and Humidity Uniformity Tests
11.9.2 Test Procedures Temperature and Humidity
11.9.3 Acceptance
11.9.4 Reporting
11.10 Electrostatic Tests
11.10.2 Test Procedures Measurement of Surface Charge Level
11.10.3 Test Procedures Surface Resistance Tests
11.10.4 Test Procedures Ion Generator Test
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11.10.5 Test Procedures Measurement of Offset Voltage
11.10.6 Acceptance
11.10.7 Reporting
11.11 Conductivity Tests
11.11.2 Test Procedures Floor Tile to Tile
11.11.3 Test Procedures Floor to Building Ground
11.11.4 Acceptance
11.11.5 Reporting
11.12 Electromagnetic Interference (EMI) Tests
11.12.3 Acceptance
11.12.4 Reporting
11.13 Air Change Rate (ACH) Tests
11.13.3 Acceptance
11.13.4 Reporting
11.14 Bench Scan Filter Leak Tests
11.14.3 Acceptance
11.14.4 Reporting
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APPENDICES
APPENDIX A
Sample CPT Specifications
APPENDIX A-1 Sample CPT Specification Microelectronics &

Semi-Conductors (Sample Specifications are available on the NEBB website) III
APPENDIX A-2 Sample CPT Specification Bio-Medical &
Pharmaceutical (Sample Specifications are available on the NEBB website)
APPENDIX B
References and Referenced Publications
VII
APPENDIX C
Engineering Formulas, Equivalents, & Examples
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TABLE OF CONTENTS
XII
PART 1 - STANDARDS
SECTION 1 - DEFINITIONS
These procedural standards have been developed using language defined by Shall, Should,
and May" as it relates to the standards and procedures described in this publication. It is
important to note these particular words throughout this publication and how they pertain to
NEBB standards and procedures.
Acceptance Criteria: The value or range of values which is compared to the measured value that will
determine if the results of the test pass or fail.
Accuracy: The accuracy of an instrument is the capability of that instrument to indicate the true value
of a measured quantity.
Aerosol (Cleanroom Use): A suspension of solid (microspheres) or liquid particles (PAO, DOP,
DEHS, etc.) in a gaseous medium used to evaluate HEPA filter integrity and/or efficiency.
Aerosol Challenge: Challenging of a filter or an installed filter system by using a test aerosol.
Airborne particle: Solid or liquid object, viable or non-viable, suspended in air.
Air Change Rate: The calculated number of times the total air volume of a defined space is replaced in
a given unit of time. This is ordinarily computed by dividing the total volume of the room supply or
exhaust air in cubic meters (cubic feet), per unit of time, by the total volume of the subject space.
As-Built Facility: A cleanroom which is complete and operating, with all services connected and
functioning, but has no production equipment or operating personnel within the facility.
As-Found Data: Data found and documented during initial testing prior to modifications of a system.
At-Rest Facility: A cleanroom which is complete with all services functioning and with production
equipment installed and capable of being operated or operating, as specified, but without operating
personnel within the facility.
Calibration: The act of comparing an instrument of unknown accuracy with a standard of known
accuracy to detect, correlate, report, or eliminate by adjustment any variation in the accuracy of the
tested instrument.
Certificate of Compliance (Conformance): A written statement, signed by a qualified party, attesting
that the items or services are in accordance with specified requirements, and accompanied by additional
information to substantiate the statement.
Certification: The process of verifying compliance to meet the established acceptance criteria.
SECTION 1
DEFINITIONS
Classification: A specified level of airborne particulate cleanliness applicable to a cleanroom or clean

zone, expressed in terms of a cleanliness class, in accordance with a referenced standard.
Cleanroom: A specially constructed room in which the air supply, air distribution, filtration of air supply,
materials of construction, and operating procedures are regulated to control airborne particle
concentrations to meet appropriate cleanliness levels and other relevant parameters (e.g. temperature,
humidity, pressure, etc.) as defined by ISO 14644, or any other regulatory entity.
Cleanroom Installation: Cleanroom or one or more clean zones, together with all associated
structures, air-treatment systems, services, and utilities.
Cleanroom Performance Testing (CPT): The act of evaluating the performance of a cleanroom by
performing a series of defined tests with prescribed procedures and reporting requirements.
Clean Zone: A defined or dedicated space in which the concentration of airborne particles is controlled
to specified limits or cleanliness levels and other relevant parameters (e.g. temperature, humidity,
pressure,) as defined by ISO 14644, or any other regulatory entity.
Contamination: The presence of any unwanted substance, material or energy which adversely affects
a product or procedure in a cleanroom.
Controlled Environment: A work space or room in which limited access or special environmental
controls are designed into operational standards.
Counting Efficiency: The ratio of the reported concentration of particles in a given size range to the
actual concentration of such particles.
Designated Leak: A leak from a HEPA/ULPA filter or filter bank that should be detectable during
scanning of the filter installation with a discrete particle counter or aerosol photometer. When using a
discrete particle counter, the designated leak is characterized by a designated number of counts,
chosen to establish statistical probabilities related to its detection. When using a photometer a
designated leak is normally characterized by a reading that is greater than 0.01% of the upstream
challenge.
Differential Pressure (P): The difference between two pressures measured between a sample
point and reference point.
Deficiency:
system.
Any circumstance that adversely affects the specified performance of a device or
Dioctyl Phthalate (DOP): A liquid plasticizer that can be used in an aerosolized form to challenge
HEPA filters
Dilution System: A device where a known volume of aerosol is mixed with clean air in a known
volumetric ratio to reduce concentration.
Effective Filter Face Area: The total area of active filter face through which air passes.
SECTION 1
DEFINITIONS
Filter Face Velocity:

Measuring the airflow velocity using an appropriate velocity measuring
instrument at a specific distance from the filter face or by dividing the airflow volume by the effective
filter face area.
Frequency: As pertains to sound and vibration, the number of vibrations or waves or cycles of any
periodic phenomenon per second. In noise control of cleanrooms, interest lies in the audible frequency
range of 20 to 20,000 Hz (cycles per second).
HEPA Filter (High Efficiency Particulate Air Filter): An extended media, dry-type filter in a rigid
frame having a minimum particle-collection efficiency of 99.97 percent for 0.3 micron particulate at a
rated airflow. HEPA filters may be specified by type and grade according to the current edition of IESTRP-CC001 HEPA and ULPA Filters. When the term HEPA filter is used in this publication, the term
generally will apply to both HEPA and ULPA filters, unless the efficiency is stated and an ULPA filter
specifically is required.
Isokinetic Sampling: Any technique for collecting airborne particulate matter in which the collection is
so designed that the air stream entering the probe is an airflow velocity that is near to, or equal to, that
of the air passing into and around and outside the probe.
Laskin Nozzle:
compressed air.
A nozzle used for the generation of a heterogeneous DOP or PAO aerosol by
Leak: Penetration of contaminates that exceed an expected value of downstream concentration

through defects or lack of integrity.
May: Used to indicate a course of action that is permissible as determined by the NEBB Certified CPT
Firm.
Micrometer (Micron): A unit of measurement equal to one-millionth of a meter or approximately
0.00003937 inch. (25 microns are approximately 0.001 inch).
Microspheres (Polystyrene Latex Spheres PSL): Manufactured highly uniform monodispersed
particles in an aqueous solution. These particles are used to generate an aerosol challenge medium for
testing cleanroom filters.
Mixed Airflow Cleanroom: A hybrid cleanroom consisting of a combination of unidirectional airflow
and non-unidirectional airflow within the same room.
NEBB Certified CPT Firm: A NEBB Certified (CPT) Firm is a firm that has met and maintains all the
requirements of the National Environmental Balancing Bureau (NEBB) for firm certification in
Cleanroom Performance Testing and is currently certified by NEBB. A NEBB Certified CPT Firm shall
employ at least one NEBB Certified CPT Professional in a full time management position.
NEBB Certified CPT Report: The data presented in a NEBB Certified CPT Report accurately
represents system measurements obtained in accordance with the current edition of the NEBB
Procedural Standards for Certified Testing of Cleanrooms. Any variances from design, specified or
agreed tolerances, are noted in the CPT report project summary.
SECTION 1
DEFINITIONS
NEBB Certified CPT Professional: A NEBB Certified CPT Professional is a full time employee of
the firm in a management position who has successfully passed the professional level written and
practical qualification examinations and maintains the Certified CPT Professional re-certification
requirements of NEBB.
NEBB Certified CPT Technician: A NEBB Certified CPT Technician is a full time employee of the
firm who has met the technician level experience requirements of NEBB and has successfully passed
the technician level written and practical qualification examinations. A NEBB Certified CPT
Technician shall be supervised by a NEBB Certified CPT Professional. (Supervision is not intended
to infer constant oversight. A NEBB Certified CPT Technician is capable of performing assigned
tasks with periodic supervision.)
Non-Unidirectional Airflow Cleanroom: Air distribution where the supply air entering the clean zone
mixes with the internal air by means of induction.
Occupancy State(s): Three conditions of various stages of testing of a cleanroom: As-Built, At-Rest,
and Operational.
Operational Facility: A cleanroom which is complete with all services functioning, and with
production equipment installed and operating under normal conditions with all operating personnel
present.
Particle: A solid or liquid object which, for purposes of classification of air cleanliness, falls within a
cumulative distribution that is based upon a threshold (lower limit) size in the range from 0.1 to 5
microns (m).
Particle Count: Concentration expressed in terms of the number of particles per unit volume of air.
Normally associated with the particles in the cleanroom or clean zone.
Particle Counter (Discrete): A light scattering instrument with display or recording means to count and
size discrete particles in air.
Particle Size: An expression for the size of solid or liquid particles expressed as the apparent
maximum linear dimension or diameter of the particle.
Particle Size Distribution: Cumulative distribution of particle concentration as a function of particle
size.
Poly-Alpha Olefin (PAO): A synthetic, non-corrosive, non-mutagenic liquid compound which can be
used to generate an aerosol to challenge HEPA filters.
Precision: The ability of an instrument to produce repeatable readings of the same quantity under the
same conditions. The precision of an instrument refers to its ability to produce a tightly grouped set of
values around the mean value of the measured quantity.
Procedure: The approach to and execution of a sequence of work operations to yield a repeatable
and defined result.
Range: The upper and lower limits of an instruments ability to measure the value of a quantity for
which the instrument is calibrated.
SECTION 1
DEFINITIONS
Resolution: The smallest change in a measured variable that an instrument can detect.
Room Velocity: The average air velocity in the occupied zone at a specified distance downstream of
the entrance zone.
Scanning: A method for disclosing leaks in HEPA or ULPA filter units in which the probe inlet of an
aerosol photometer or discrete particle counter is held approximately 25 mm (1 inch) from the filter face
and moved in overlapping strokes across the test area at a rate based on the leak penetration to be
detected and the upstream challenge concentration.
Shall: The term is used to indicate mandatory requirements to be followed strictly in order to conform
to the standards and procedures and from which no deviation is permitted. Note: In the event unique
circumstances prevent a required action from being fulfilled, a notation shall be included in the CPT
report explaining the exception. For example, such notation could be one of the following: Not
Available, Not Applicable, or Not Accessible. The simple notation N/A without definition is not
allowed.
Should: The term is used to indicate that a certain course of action is preferred but not necessarily
required.
Standard: A required qualification, action, or result for CPT work.
Testing, Adjusting, and Balancing (TAB): TAB is a systematic process or service applied to
heating, ventilating and air-conditioning (HVAC) systems and other environmental systems to achieve
and document air and hydronic flow rates.
Testing Intervals:
6 Months: Testing that occurs at an average interval not exceeding 183 days throughout
periods of operation use, subject to no interval exceeding 190 days.
Threshold Size: A selected minimum particle size of particle counter measurement capability; the
smallest particle size discrimination.
ULPA (Ultra-Low Penetration Air) filters: An extended-medium dry-type filter in a rigid frame having
a minimum particle collection efficiency of 99.999% for particles in the size range of 0.1 to 0.2 m.
Ultra-fine particles: A particle with an equivalent diameter less than 0.1micron (m).
.
Unidirectional Airflow Cleanroom: Controlled airflow through the entire cross-section of a clean zone
with a uniform velocity and approximately parallel air stream that is no greater than 14 degrees from
plumb.
SECTION 1
DEFINITIONS
Unidirectional Flow (Parallel Airflow): Controlled airflow through the entire cross-section of a clean
zone with a steady velocity and approximately parallel streamlines. Fluid flow in which particles move in
a smooth path substantially parallel to the paths followed by all other particles.
Uniform Airflow: Airflow in which the relative standard deviation of velocities or volumes does not
exceed 15 percent.
Upstream Particle Concentration: Number of individual particles per unit volume of air associated
with the number of particles upstream of the HEPA filter.
Validation: Establishing documented evidence that a process or system, when operated within
established parameters can perform effectively and reproducibly to produce a product meeting its
predetermined specifications and quality attributes.
Work Station: An open or enclosed work surface with direct HEPA filtered air supply.
Work Zone: An area within the cleanroom which is designated for clean work and for which CPT is
required. The work zone shall be identified by an entrance and exit plane normal to the airflow (where
there is unidirectional airflow).
SECTION 2 - NEBB PROGRAM,

QUALITY CONTROL AND
COMPLIANCE
2.1 NEBB PROGRAMS
The National Environmental Balancing Bureau (NEBB) is a not-for-profit organization founded in 1971
to:
a) develop standards, procedures and programs for the performance of cleanroom certification,
testing, adjusting and balancing of environmental systems, measurement of sound and
vibration of building systems, commissioning of building systems, retro-commissioning of
existing building systems and performance testing of fume hoods,
b) promote advancement of the industry through technical training and development, and
c) operate programs to certify firms and individuals who meet and maintain NEBB standards with
integrity.
Additional information on NEBB Programs is available at www.nebb.org.
2.1.1 NEBB DISCIPLINES
NEBB establishes and maintains standards, procedures, and specifications for work in its various
disciplines, which include:
a)
b)
c)
d)
e)
f)
g)
Cleanroom Performance Testing (CPT)

Testing, Adjusting, and Balancing (TAB) of Air and Hydronic Systems
Sound (S) Measurement
Vibration (V) Measurement
Building Systems Commissioning (BSC)
Retro-Commissioning (RCx-EB)
Fume Hood Testing (FHT)
Each discipline is anchored by a NEBB Procedural Standards manual that provides guidelines for
work to be performed. NEBB also has created technical manuals, training materials and programs,
and seminars to enhance and support each discipline.
2.1.2 CERTIFICATION OF FIRMS
NEBB certifies firms that meet certain criteria, ensuring strict conformance to its high standards and
procedures. Among other requirements, NEBB Certified Firms must document a record of
responsible performance, own a complete set of instruments required for the sophisticated techniques
and procedures necessary to perform certification tests in the various disciplines and have a NEBB
Certified Professional as a full-time employee.
2.1.3 CERTIFICATION OF PROFESSIONALS
NEBB also establishes professional qualifications for the supervision and performance of work in its
various disciplines. NEBB Certified Professionals must have extensive experience, and they must
pass appropriate, college-level written examinations and demonstrate certain practical working
SECTION 2
NEBB PROGRAM, QUALITY CONTROL
AND COMPLIANCE
knowledge, technical decisions and proficiency in the use of instruments required for the various
disciplines.
2.1.4 CERTIFICATION OF TECHNICIANS
NEBB also certifies technicians who must possess certain background and experience as well as
pass rigorous written and practical examinations. NEBB Certified Technician status is maintained by
continued employment with a NEBB Certified Firm.
2.1.5 RECERTIFICATION REQUIREMENTS
Through the recertification procedures, the firm must verify that its NEBB Certified Professional is still
on staff and that it continues to own a complete set of instruments that are in current calibration. In
addition, the firm's NEBB Certified Professional renews his or her certification annually. Among other
requirements, Certified Professionals and Certified Technicians must keep abreast of developments in
their discipline by attending and successfully completing continuing education seminars annually.
2.2 QUALITY ASSURANCE PROGRAM - CONFORMANCE CERTIFICATION

The credibility of NEBB is built by maintaining integrity through high standards, quality programs, and
demonstrated capabilities of its certified firms. As further assurance, NEBB offers a Quality
Assurance Program to guarantee that the work will be accomplished in accordance with its standards.
NEBBs Quality Assurance Program applies to each project. It assures that the NEBB Certified Firm
will perform specified services in conformity with the current applicable NEBB Procedural Standards.
2.2.1 PROGRAM ADVANTAGES
The NEBB Quality Assurance Program affords building owners, architects, engineers and other
agents a reliable basis for specifying work within the various disciplines of NEBB. The program
promotes proper execution of projects by ensuring compliance with NEBB standards and procedures.
2.2.2 NEBB QUALITY ASSURANCE PROGRAM CERTIFICATE
The NEBB Quality Assurance Program Conformance Certificate is not required, but is available for
any project.
2.3 QUALITY CONTROL AND COMPLIANCE

Building owners are entitled to a professional service by every NEBB Certified Firm on every project,
whether the job is NEBB-specified or not. It is the responsibility of the NEBB Certified Firm and its
NEBB Certified Professional to establish and maintain procedures and practices that will assure a
consistent pattern of high quality work on all projects. This point cannot be overemphasized.
2.3.1 CLEANROOM WORK COMPLIANCE
The scope of work shall be performed as specified in the contract documents, or as agreed to
between the Owner / Buyer and the NEBB Certified CPT Firm. Each relevant or applicable item as
identified in the contract documents by description, or by reference, shall be performed and
documented in the report. Data presented in a report shall provide an accurate quantitative record of
system measurements and information.
References to desired procedures may include statements such as "the work will be performed in
accordance to NEBB Standards." When specifications indicate that the work shall be performed in
accordance with NEBB standards, the procedures will conform to the current edition of the NEBB
SECTION 2
AND COMPLIANCE
Procedural Standards for Certified Testing of Cleanrooms and the work must be performed by a
NEBB Certified CPT Firm.
2.4 CERTIFIED CPT PROFESSIONAL RESPONSIBILITIES

It is the responsibility of the NEBB Certified CPT Professional to control the quality of the work. This
means that the NEBB Certified CPT Firm, through its NEBB Certified CPT Professional, shall satisfy
the project testing requirements exclusive of acceptance criteria or guaranteeing performance.
2.4.1 EXECUTION OF CPT PROCEDURES
The NEBB Certified CPT Professional shall have project responsibility, which includes authority to
represent the NEBB Certified CPT Firm. Examples of project responsibility may include labor
decisions, negotiating change orders, committing to contract interpretations and implementing
changes in job schedules.
The NEBB Certified CPT Professional has the responsibility to assure that the cleanroom
performance tests have been completed and reported in accordance with these CPT Procedural
Standards and the contract documents to assure the accuracy of all data that is included in the final
report. Factors such as technician training, instrument use, coordination, supervision, work
instructions, and project communication play a critical role in achieving this requirement.
2.4.2 TECHNICIAN TRAINING
The NEBB Certified CPT Professional has a responsibility to assure that technicians performing the
work are properly trained and possess sufficient skills. Areas that should be stressed are CPT
procedures, instrument use and maintenance, coordination, supervision, and project communication.
2.4.3 CLEANROOM PROCEDURES TRAINING
NEBB Certified CPT Technicians must be prepared to completely measure and record data in the
manner specified in the NEBB Procedural Standards for Certified Testing of Cleanrooms. It is
mandatory that NEBB Certified CPT Technicians possess the ability to perform the specific tasks and
procedures required for each project. An understanding of items such as HVAC system operation,
operating characteristics, cleanroom protocol, etc. are important, and technicians should possess
rudimentary knowledge of all related systems and procedural considerations. This may require
periodic training to promote knowledge and skill development as well as to facilitate the transfer of
knowledge and basic skills in the use of new technology.
2.4.4 INSTRUMENT USE AND MAINTENANCE
NEBB Certified CPT Technicians shall possess knowledge and skill in the proper use and care of
instruments required to perform the work. This shall include a thorough understanding of the
operating principles, the range and accuracy of the instrument requirements as specified in the NEBB
Procedural Standards for Certified Testing of Cleanrooms and the proper use of equipment and
instruments. Considerations for the delicate nature of many of the instruments typically used, as well
as the adverse effects of dirt, shock, jarring movements and exceeding rated capacities, shall be
addressed along with the proper methods for storing and transporting the instruments.
2.4.5 COORDINATION / SUPERVISION
The NEBB Certified CPT Professional shall be responsible for directing technicians in performing the
work. Instructions may delineate items such as the scope of work, location and quantity of
measurements, location and quantity of sample locations, leak testing procedures, design, specified
SECTION 2
AND COMPLIANCE
or agreed criteria, etc. so that field personnel may know exactly what to do and what is required of
them.
2.4.6 PROJECT COMMUNICATION
The NEBB Certified CPT Professional shall report on progress made toward work completion, when
required, as well as report and address problems if encountered. When a problem exists, the NEBB
Certified CPT Professional should notify the appropriate project personnel. The NEBB Certified CPT
Professional may provide input as to the cause of the problem and recommend possible solutions.
2.4.7 FIELD WORK COMPLETION
The NEBB Certified CPT Professional shall determine when the cleanroom testing work has been
completed, and when to submit the final report. The field work is complete when the field testing
scope of work as specified in the contract documents or as agreed to between the Owner / Buyer and
the NEBB Certified CPT Firm is achieved.
2.4.8 COMPILATION AND SUBMISSION OF FINAL CLEANROOM REPORTS
Reports shall include information and data to provide an accurate quantitative record of system
measurements and information. Reports also shall include notes and comments, as appropriate, to
provide the reviewer with additional details related to the test procedure, system operation and
results. Reports shall meet the criteria listed in Section 5 or as agreed between the Buyer / Owner
and the NEBB Certified CPT Firm.
The certification page shall bear the stamp of the NEBB Certified CPT Professional. The stamp on the
certification page shall be signed as evidence that the NEBB Certified CPT Professional has
personally reviewed and accepted the report. Signature stamps are specifically prohibited.
2.4.9 PROJECT COMPLETION
The project completion shall be defined by having all field testing and project document deliverables
completed and submitted to the Owner / Buyer.
10
SECTION 3 RESPONSIBILITIES
3.1 INTRODUCTION
Many approaches can be taken to deliver a successful cleanroom project. In order to maximize value
and benefits derived from cleanroom testing, it is important to understand that the owner/buyer,
design professionals and other construction team members have responsibilities that will affect the
outcome of the testing process.
The following outline represents NEBBs recommended practices that may take place on a
conventional design/bid or buy/construct delivery project or on a direct procurement project between
the Owner / Buyer and the NEBB Certified CPT Firm. While other delivery approaches will exist, the
overall concept of the delineation of responsibilities remains. The Owner / Buyer shall be the
responsible party that dictates the procedures that are employed.
3.2 OWNER / BUYER AND DESIGN AND CONSTRUCTION TEAM

RESPONSIBILITIES
3.2.1 OWNER / BUYER AND DESIGN PROFESSIONAL RESPONSIBILITIES
It is recommended that the Owner / Buyer and / or contract documents shall:
a. Specify the tests to be performed, the parameters to be measured and the acceptable
tolerances. NEBB standards and procedures define industry best practices to perform the
testing.
b. Define who retains the services of the NEBB Certified CPT Firm and require that the NEBB
Certified CPT Firm be retained early in the construction process.
c. Define the applicable standards, cleanliness classification(s), acceptance criteria, etc. prior to
submission of project fees; i.e. ISO Class 4 at 0.3 microns (m).
d. Clearly identify on the architectural, mechanical and electrical plans and in the specifications,
the system components required for cleanroom testing; i.e. pressure relationships, cleanroom
reflected ceiling plans, cleanroom floor plans, etc.
e. Specify that the building and/or HVAC control system be commissioned and documented per
NEBB commissioning standards and procedures before the cleanroom testing work begins.
f.
Specify that the air and water systems be Tested, Adjusted and Balanced (TAB) and
documented per NEBB Procedural Standards for Testing, Adjusting, Balancing of
Environmental Systems before the cleanroom testing work begins.
g. Specify that the building control system firm provides access to hardware and software, or
onsite technical support required to assist the cleanroom testing effort. The hardware and
software or the onsite technical support shall be provided at no cost to the NEBB Certified
CPT Firm.
11
SECTION 3
RESPONSIBILITES
h. Provide adequate access to all equipment and components required by the cleanroom testing
process.
i.
Completely define validation / commissioning support responsibilities for the NEBB Certified
CPT Firm.
3.2.2 OWNER / BUYER AND / OR CONSTRUCTION TEAM RESPONSIBILITIES

It is recommended that the Owner / Buyer and/or construction team shall:
.
a. Provide the NEBB Certified CPT Firm with a complete set of conformed contract documents
(drawings, specifications, and approved submittals), including all current approved change
orders and contract modifications.
b. Develop a project schedule with the input of the NEBB Certified CPT Firm that coordinates the
work of other disciplines and provides adequate time in the construction process to allow
successful completion of the cleanroom testing and certification work.
c. Notify the NEBB Certified CPT Firm of all schedule changes.
d. Ensure that the cleanroom envelope is complete.
e. Ensure that all necessary mechanical, electrical and HVAC work is complete and is safe to
operate. Permanent electrical power shall be complete and all electrical systems shall be
properly installed in accordance with all applicable codes to ensure the safety of all
construction personnel.
f.
Complete the installation, programming (including design parameters and graphics),

calibration and startup of all building control systems that affect the cleanroom operation, and
verify that the building control system provider has commissioned and documented their work.
g. Require that the building control system firm provide access to hardware and software, or
CPT Firm.
h. Define the cleanroom entry protocol; i.e. gowning, wipe-down procedures, etc.
i.
Complete the TAB work prior to the NEBB Certified CPT Firm performing the necessary
cleanroom tests.
j.
Provide the NEBB Certified CPT Firm with a HEPA filter layout, and where required, serial
number and location of each filter within all cleanrooms.
3.2.3 NEBB CERTIFIED CPT FIRM RESPONSIBILITIES

The NEBB Certified CPT Firm SHALL:
a. Perform the scope of work as specified in the contract documents, or as agreed to between
the Owner / Buyer and the NEBB Certified CPT Firm.
12
SECTION 3
RESPONSIBILITES
b. Follow the current NEBB CPT standards and procedures when performing the cleanroom
tests.
c. Communicate on a regular basis through proper channels, items relating to design,
installation, or function that prevent the NEBB Certified CPT Firm from achieving completion of
the cleanroom tests in accordance with the current edition of the NEBB Procedural Standards
for Certified Testing of Cleanrooms.
d. Perform the specified validation/commissioning support requirements.
e. Publish a NEBB Certified CPT Report of final conditions that accurately reflect the
measurements and conditions of the cleanroom tests performed as specified in the contract
documents, or as agreed to between the Owner / Buyer and the NEBB Certified CPT Firm.
13
SECTION 3
RESPONSIBILITES
14
SECTION 4 - STANDARDS FOR

EQUIPMENT,
INSTRUMENTATION AND
CALIBRATION
4.1 MINIMUM INSTRUMENTATION
A NEBB Certified CPT Firm will use a variety of instrumentation to perform the specified cleanroom
tests on a project. It is the responsibility of the NEBB Certified CPT Firm to use on a project
appropriate instrumentation that meets the requirements of TABLE 4-1 and TABLE 4-2. TABLE 4-1
lists the minimum instrumentation that a NEBB Certified CPT Firm SHALL own and maintain to
perform the primary cleanroom tests. TABLE 4-2 lists the minimum instrumentation that a NEBB
Certified CPT Firm SHOULD own and maintain to perform the optional secondary cleanroom tests.
Instrumentation used on a NEBB project shall be in proper operating condition and shall be used in
accordance with the manufacturers recommendations.
4.2 RANGE AND ACCURACY

A NEBB Certified CPT Firm shall possess instruments for each function and range listed in Table 4-1.
Each instrument shall have been specifically designed to meet the description criteria of the function.
This criterion may include such features as range, accuracy, resolution, capacity, etc. Instrumentation
with multiple capabilities shall be accepted for more than one function when submitting documentation
for a firms certification, providing that each separate function meets NEBB requirements. Information
and data regarding description of all submitted instrumentation for the stated functions shall be
available from the manufacturer.
The accuracy and range as reported by the instrument manufacturer shall be verified by a testing
laboratory traceable to the National Institute of Standards and Technology (NIST) or equivalent
institute in countries other than the United States. Calibration requirements for each function are
specified in Table 4-1 and 4-2 and shall be met.
Firms with multiple sets of instrumentation shall comply by calibrating all instrumentation used by the
firm on cleanroom projects in accordance with Tables 4-1 and 4-2.
NEBB Certified CPT Professionals must understand the importance of using accurate
instrumentation in the field, and shall be prepared to have witnesses verify their work with the
NEBB Certified CPT Firms calibrated instruments. Results of the data verification shall
validate the accuracy of the instrumentation used to perform the work.
Instruments shall be used in accordance with manufacturers recommendations. The most suitable
instrument, or combination of instruments, should be employed for a particular measurement or
reading.
15
SECTION 4
STANDARDS FOR EQUIPMENT,
INSTRUMENTATION AND CALIBRATION
TABLE 4-1 NEBB MINIMUM INSTRUMENTATION REQUIREMENTS

Test
Airflow Velocity and Uniformity Test
(One of the following Shall be provided)
(Sections 10.3, 10.5, & 10.6)
Equipment/
Instrumentation
Anemometer
(Direct Air
Velocity
Measurement)
Description
A digital anemometer capable of meeting
the following requirements:
Range: 0.25 12.5 m/s (50 - 2500 fpm)
Accuracy: 5% of reading 0.50 m/s (100
fpm) or greater
Accuracy: 10% of reading 0.50 m/s (100
fpm) or less
Resolution: 0.005 m/s (1.0 fpm)
Calibration
Interval
12 Months
Manometer
(Indirect Air
Velocity
Measurement)
A digital manometer capable of meeting

Range*: 0.25 12.5 m/s (50 - 2500 fpm)
Accuracy*: 5% of reading
Resolution*: 0.1 m/s (20 fpm)
(* Based on conversion of velocity
pressure to velocity at the local
atmospheric conditions)
12 Months
Tube Array
A tube array with the following:

Range: 0.13 12.5 m/s (25 to 2500 fpm)
Accuracy: 3% of reading 0.04 m/s from
0.25 to 40 m/s ( 7 fpm from 50 to 8000
fpm.
Not
Required
Pitot Tube or
Single-Point
Probe
Range: 0.13 12.5 m/s (25 to 2500 fpm)

0.25 to 40 m/s ( 7 fpm from 50 to 8000
fpm.
Not
Required
Airflow Volume and Uniformity Test

(Section 10.4 & 10.8)
Direct Reading
Hood
A flow capture hood with an integral

analog or digital manometer capable of
meeting the following requirements:
Range: 50 1000 L/s (100 - 2000 cfm)
Accuracy: 5% of reading, 2.5 L/s
(5% of reading, 5 cfm)
Resolution: (Digital): 0.5 L/s (1.0 cfm)
(Analog): 2.5 L/s (5.0 cfm)
12 Months
Airflow Volume and Uniformity Test

(Section 10.9)
Manometer

Range: 0.25 12.5 m/s (50 - 2500 fpm) *
Accuracy: 5% of reading
Resolution: 0.1 m/s (20 fpm)
12 Months
Pitot Tube or
Single-Point
Probe
Range: 0.13 12.5 m/s (25 to 2500 fpm)

0.25 to 25 m/s ( 7 fpm from 50 to 5000
fpm).
Not
Required
16
SECTION 4
TABLE 4-1 NEBB MINIMUM INSTRUMENTATION REQUIREMENTS (CONT.)

Test
Leak Testing
(w/Photometer)
(Section 10.11, 10.13 & 11.14)
Equipment/
Instrumentation
Aerosol
photometer
Description
The instrument shall have a threshold
-3
sensitivity of 10 micrograms per liter of
challenge aerosol particles and be capable
of measuring concentrations over a range
of 105 times the threshold sensitivity.
Calibration
Interval
12 Months
Sample flow rate shall be

28.3 L/min (1 cfm) with a probe inlet sized
to provide isokinetic sampling. Readout
shall be either linear or logarithmic with an
accuracy of 1% of full scale of the selected
range.
Leak Testing
(w/Particle Counter)
(Section 10.12, 10.13 & 11.14)
Aerosol Generator
A device that can aerosolize either a

polydispersed or a monodispersed
artificial particle medium for filter integrity
testing, including Laskin nozzle type,
thermal generator, atomizer, etc.
Not
Required
Scanning Probes
Scanning probe (square or rectangular)

fitted with a sampling tube whose length
does not exceed 8 meters (25 feet).
Not
Required
Particle Counter
(Scanning)
A light scattering instrument with display or

recording means to count and size
discrete particles in air, as defined by
ASTM F50-69. Instruments of this type
shall provide for a minimum sampling flow
rate of 28.3 L/min (1.0 cfm) and a
threshold size discrimination of a minimum
of 0.3 micrometer (microns) in size.
12 Months
Scanning Probes
Near-Isokinetic (square or rectangular)

scanning probe fitted with a sampling tube
no longer than 8 meters (25 feet).
Not
Required
Aerosol Generator

thermal generator, atomizer, etc.
Not
Required
Diluter
A device used with the scanning particle

counter to sample the aerosol challenge
upstream of a filter under test. The
resulting counts after dilution should not
exceed 100,000 particles.
12 Months
17
SECTION 4
TABLE 4-1 NEBB MINIMUM INSTRUMENTATION REQUIREMENTS (CONT.)

Test
Airborne Particle Count Cleanliness
Classification Test
(Sections 10.14 and 10.15)
Room Pressurization Test

(Section 10.16)
Equipment/
Instrumentation
Particle Counter
Description
shall provide for a minimum sampling flow
rate of 28.3 L/min (1 cfm) and a threshold
size discrimination of a minimum of 0.3
micrometer in size. The unit shall be
provided with an isokinetic sampling probe
to maintain the probe inlet velocity at the
test airflow rate.
Calibration
Interval
12 Months
Sampling Probes
Sampling probe fitted with a sampling tube

no longer than 8 meters (25 feet).
Not
Required
Manometer
An analog or digital manometer capable of

Range: 0 - 125 Pa (0 0.50 in.w.g.)
Resolution: 2.5 Pa 250 Pa
(0.01 in.w.g. <1 in.w.g.)
25 Pa > 250 Pa
(0.1 in.w.g. >1 in.w.g.)
12 Months
TABLE 4-2 NEBB MINIMUM (SHOULD) INSTRUMENTATION REQUIREMENTS

Test
Airflow Parallelism Test
(Section 11.2)
Equipment/
Instrumentation
Test Medium
Description
A non-contaminating smoke vapor source,
streamers, thread or string
Calibration
Interval
Not
Required
Support Stand &

Support Stand
with Pointer
A device for positioning the test medium at

the specified location and height that is
aerodynamically designed to yield the
least impact to room airflow.
Not
Required
Plumb Bob or
Spirit Level
A small mass of heavy material

suspended by a line and used to ascertain
a vertical line.
Not
Required
Tape Measure
Linear measurement device with a

minimum resolution of 1.0 mm or 1/16 in.
Not
Required
18
SECTION 4
TABLE 4-2 NEBB MINIMUM (SHOULD) INSTRUMENTATION REQUIREMENTS (CONT.)

Test
Recovery Test
(Section 11.3)
Equipment/
Instrumentation
Aerosol Generator
Aerosol
photometer
Description
thermal generator , ultrasonic humidifier,
atomizer, etc.
The instrument shall have a threshold
-3
sensitivity of 10 micrograms per liter of
challenge aerosol particles and be capable
of measuring concentrations over a range
of 105 times the threshold sensitivity.
Calibration
Interval
12 Months
12 Months
Sample flow rate shall be

28.3 L/min (1 cfm) with a probe inlet sized
to provide isokinetic sampling. Readout
shall be either linear or logarithmic with an
accuracy of 1% of full scale of the selected
range.
Lighting Level and Uniformity Test

(Section 11.4)
Particle Counter

shall provide for a sampling flow rate of
28.3 L/min (1 scfm) and a threshold size
discrimination of a minimum of 0.2
micrometer in size. The unit shall be
provided with an isokinetic sampling probe
to maintain the probe inlet velocity at the
test airflow rate.
12 Months
Light Meter
A portable photo-electric illumination meter

approved for field measurement in
accordance with the Illumination
Engineering Society Lighting Handbook
(IES).
12 Months
19
SECTION 4

Test
Sound Level Test
(performed w/SLM)
(Section 11.5)
Sound Level Test

(performed w/Real Time Analyzers)
(Section 11.5)
Equipment/
Instrumentation
Sound level meter
(SLM)
Description
Sound level meter (SLM) for sound
pressure measurements shall meet the
Type 1 or Type 2 requirements specified in
the most current version of ANSI S1.4
Calibration
Interval
12 Months
Full and Third

Octave Filters
Filters for sound pressure measurements

shall meet the requirements specified in
12 Months
Acoustic
Calibrators
Calibrators for sound pressure calibration

12 Months
Real Time
Analyzer
Real Time Analyzer for sound pressure

measurements shall meet the minimum
requirements as specified in ANSI S1.4
and S1.11 and,
Lines of resolution 400
Frequency range capability = 0 20.0 kHz
True dynamic range 70 dB
Sum and exponential averaging
Peak hold function
Memory for storage of measurements
12 Months
Full and Third

Octave Filters
Full and Third Octave Filters for sound

pressure measurements shall
meet the requirements specified in the
most current version of ANSI S1.11
12 Months
Acoustic
Calibrators
Acoustic Calibrators
for sound pressure calibration
the most current version of ANSI S1.40.
12 Months
20
SECTION 4

Test
(performed w/ Vibration Meter)
(Section 11.6)
General Temperature and moisture

Uniformity Test
(Section 11.8)
Equipment/
Instrumentation
Vibration Meter
Description
Vibration Meter for vibration
requirements as specified below:
Displacement: 0.00254 mm to 2.54 mm
(0.1 to 100 mils),
Velocity: 0.13 - 2500 mm/s (0.005 to 100
in/sec)
Acceleration: 0.098 980 m/s (0.01 to
100 Gs)
Frequency Range 1 to 200 Hz (0 to
12,000 CPM)
Frequency Resolution Narrowband 1 Hz
Calibration
Interval
12 Months
Accelerometers /
Transducers
Accelerometers / Transducers for

vibration measurements shall have the
following minimum specifications:
Sensitivity (10 %) 100 mV/G
Measurement Range = 490m/s(50 G)
peak
Frequency Range = 1 to 1000 Hz at 5 %
Mounted Natural Frequency 30,000 Hz
12 Months
Vibration
Integrators
Vibration Integrators for SLM for vibration

requirements as specified below:
Displacement: 0.003 - 2.5 mm (0.1 to
100mils)
Velocity: 0.13 2500 mm/s (0.005 to 100
in/sec)
Acceleration: 0.098 980 m/s (0.01 to
100 Gs)
Frequency Range: 1 to 10,000 Hz
Frequency Resolution:
1/3-Octave 12.5 to 20,000 Hz
12 Months
Vibration
Calibrators
Vibration Calibrators for vibration

calibration of SLM shall have the following
minimum specifications
Operating Frequency = 159.2 Hz
Acceleration Output = 1.00 G rms 3%
Distortion (with 0 to 100 gram load) 3%
12 Months
Air Temperature
Measurement
Instrument
An analog or digital thermometer capable

of meeting the following requirements:
Range: 4.5C-38C (40F-100F)
Resolution: 0.1C (0.2F)
12 Months
Humidity
Measurement
Instrument
An analog or digital hygrometer capable of

Range: 10% - 90% RH,
Accuracy: 2% RH,
Resolution: 1% RH
12 Months
21
SECTION 4

Test
Equipment/
Instrumentation
Description
Comprehensive Temperature and

Moisture Uniformity Test
(Section 11.9)
Data Recorder Temperature
Electronic thermometers and temperature

sensors with readout devices capable of
Range: 4.5C - 38C, (40F - 100F)
Accuracy: 0.05C, (0.1F)
Resolution: 0.05C. (0.1F)
Instruments shall be capable of recording
temperature and humidity or dew point at
specified time intervals and time periods.
Data Recorder Humidity
Humidity measuring instruments and

sensors used with readout devices capable
Range: 10% - 90%,
Accuracy: 0.1%,
Resolution: 0.1%
Instruments shall be capable of recording
temperature and humidity or dew point at
specified time intervals and time periods.
12 Months
Electrostatic
Voltmeter
Electrostatic Field
meter
Voltmeter or field meter shall have a range

of 8.163 kv/cm (19.99 kv/inch) with an
accuracy of 5% and a response time of
less than 2 seconds for 0 kv to 5 kv
12 months
Ohmmeter
Ohmmeter shall have operating voltages of

10 and 100 volts (DC) under load and
current limiting circuitry. It should be
14
capable of measuring from 1 ohm to 10
ohms.
12 months
Electrodes
Electrodes shall weigh 2.27 kg (5 pounds)

and have a flat, circular contact area 64 mm
(2.5 inches) in diameter, which shall
comprise of a surface of aluminum or tin foil
0.0127 to 0.0254 mm (0.005 inch to 0.001
inches) thick, backed by a layer of rubber
6.4 mm (1/4 inch) thick and measuring 40
and 60 durometer hardness as determined
with a Shore Type A durometer (ASTM
D2240-68). At least one electrode lead shall
have a clip for connecting to ground.
12 months
Charged Plate
Monitor
Device shall have a measuring range of -5

kv to + 5 kv with an error of 5% of full
scale and a response time of 0.1 seconds.
A power supply in the instrument should
provide charging to at least 1000 volts.
Timing circuits should be capable of
measuring a discharge time from 1000
volts to 100 volts of either polarity.
12 months
Electrostatic Tests
(Section 11.10)
22
Calibration
Interval
12 Months
SECTION 4

Test
Conductivity Tests
(Section 11.11)
Electromagnetic Interference (EMI)

Test
(Section 11.12)
Air Change Rate / Hour (ACH) Test

(Section 11.13)

(Section 11.14)
Equipment/
Instrumentation
Ohmmeter
Description
Ohmmeter shall have an open circuit
voltage of 500 volts (DC) and a nominal
internal resistance of not less than 100,000
ohms.
Calibration
Interval
12 months
Electrodes
Electrodes shall weigh 2.27 kg (5 pounds)

and have a flat, circular contact area 64 mm
(2.5 inches) in diameter, which shall be
comprised of a surface of aluminum or tin
foil 0.0127 to 0.0254 mm (0.005 inch to
0.001 inch) thick, backed by a layer of
rubber 6.4 mm (1/4 inch) thick and
measuring 40 and 60 durometer hardness
as determined with a Shore Type A
durometer (ASTM D2240-68).
12 months
Magnetic Field
Meter
A magnetic field meter with a dynamic

range of 0.1 to 4000 milligauss
12 months
Magnetic Field
Sensor
A magnetic field sensor with an external,

multi-turn loop.
12 months
Direct Reading
Hood
A flow capture hood with an integral

analog or digital manometer capable of
Range: 50 1000 L/s (100 - 2000 cfm)
Accuracy: 5% of reading, 2.5 L/s
(5% of reading, 5 cfm)
Resolution: (Digital): 0.5 L/s (1.0 cfm)
(Analog): 2.5 L/s (5.0 cfm)
12 Months
Manometer

Range: 0.25 12.5 m/s (50 - 2500 fpm) *
Resolution: 0.1 m/s (20 fpm)
12 Months
Pitot Tube or
Single-Point
Probe
Range: 0.13 12.5 m/s (25 to 5000 fpm)

0.25 to 25 m/s (7 fpm from 50 to 5000
fpm.
Not
Required
Photometer
Same as Leak Testing w / photometer
12 Months
Particle Counter
Same as Leak Testing w / particle counter
12 Months
23
SECTION 4
Instrumentation with multiple capabilities shall be accepted for more than one function when
submitting documentation for a firms certification, providing that each separate function
meets NEBB requirements.
Calibrations of all instrumentation requiring calibration shall be traceable to current the National
Institute of Standards and Technology (NIST) Standards for US firms, or equivalent organizations in
other countries.
24
SECTION 5 - STANDARDS FOR

REPORTS AND FORMS
5.1 REPORTS
The NEBB Procedural Standards for Certified Testing of Cleanrooms establishes minimum
requirements of a NEBB Certified CPT Report. The standards have been developed and written
using Shall, Should, and May language. It is important to note these particular words throughout
this document and how they pertain to NEBB Procedural Standards.
NEBB does not require the use of NEBB produced forms. Customized forms are acceptable
based on the data acquisition requirements of this section. Where contract document data reporting
requirements exceed the minimum requirements of NEBB, the NEBB Certified CPT Firm is
responsible to meet the requirements of the contract documents. Where no contract documents exist,
the scope of services and reporting shall be as agreed to between the Owner/Buyer and the NEBB
Certified CPT Firm.
There may be projects where the reporting requirements may be defined by the owner or a regulatory
agency. These reporting requirements may or may not conform to the NEBB reporting requirements.
The NEBB CPT Firm shall be allowed to utilize client-specific reporting forms and methods in lieu of the
NEBB reporting requirements and sign and stamp the report if allowed or required by the Owner /
Buyer.
NEBB requires that all pages in the report shall be identified by a unique page/section number.
NEBB Cleanroom Reports shall include the following information:
A.
Report Title
B.
Report Certification
C.
Table of Contents
D.
Standard Operating Procedures (SOPs) References
E.
Report Summary / Remarks
F.
Test Forms
G.
Instrument Calibration Certificates
H.
Abbreviations
25
SECTION 5
STANDARDS FOR REPORTS AND FORMS
5.2 REQUIRED FORMS

Listed below are the requirements for each NEBB Certified CPT Report in Shall, Should, and May
language.
5.2.1 REPORT TITLE
Shall Data: The heading: Certified Cleanroom Test Report; Project Name / Address; Owner
Name/Address, NEBB Certified CPT Firm Name / Address / Certification Number.
May Data: Architect Name; Architect Address / Contact Numbers; Engineer Name; Engineer Address
/ Contact Numbers; HVAC Contractor Name / HVAC Contractor Address / Contact Numbers, etc.
5.2.2 REPORT CERTIFICATION
The certification page Shall bear the stamp of the NEBB Certified CPT Professional. The stamp on
the certification page Shall be signed as evidence that the NEBB Certified CPT Professional has
reviewed and accepted the report. Signature stamps are specifically prohibited.
Shall Data: Project Name; Test Occupancy State(s), Certifying NEBB Certified CPT Professionals
Name; Firm Name; Certification Number; Expiration Date; Certifying NEBB Certified CPT
Professionals NEBB Stamp (signed & dated); and the following exact verbiage:
"THE DATA PRESENTED IN THIS REPORT IS A RECORD OF CLEANROOM AND SYSTEM
PERFORMANCE AND WAS OBTAINED IN ACCORDANCE WITH THE CURRENT EDITION OF
THE NEBB PROCEDURAL STANDARDS FOR CERTIFIED TESTING OF CLEANROOMS, AND [edit
wording to include the appropriate standards that the cleanrooms were tested such as ISO, FS 209,
IEST RP etc.] ANY VARIANCES FROM DESIGN, SPECIFIED, OR AGREED TO CRITERIA ARE
NOTED IN THE CLEANROOM REPORT PROJECT SUMMARY."
Should Data: Disclaimer statement with the following suggested wording:
The results shown and information given in this report are certified to be accurate and complete to the
extent possible by equipment and procedures used on this date.
___(Insert Firm Name)_____________________________________ warrants that the equipment or
system listed above and / or identified in this report is operating at the specified levels as shown, at and
only at this time, and makes no other warranties, stated or implied, concerning the continued
performance, operation or safety in use of this equipment past this time.
Note: The Certification Statement and the Disclaimer Statement may be included on the report title
page or on a separate certification page.
5.2.3 TABLE OF CONTENTS
The table of contents shall serve as a guide to the organization of the cleanroom report.
Shall Data: Page / Section numbers of tests performed in the report.
26
SECTION 5
5.2.4 STANDARD OPERATING PROCEDURES (SOPs) REFERENCES

This section shall include a reference to all SOPs used during the execution of the work.
5.2.5 REPORT SUMMARY / REMARKS
A NEBB Certified CPT Report shall include a narrative synopsis of each performance test conducted.
The Summary section shall also include a description of the test occupancy state and narrative
explanation of any exceptions to the test occupancy state.
All tested items included in the NEBB CPT Report shall be clearly identified with a unique designation.
The method of identification may use schematic diagrams, mechanical plans where permissible, or a
narrative description. Each data form supplied in a NEBB CPT Report shall include the name of the
responsible technician / NEBB Certified CPT Professional who reported the information, and the time
period the data was collected.
This section also includes a listing of all deficiencies and items that exceed Contract Document
tolerances, or as agreed to criteria between the Owner / Buyer and the NEBB Certified CPT Firm, or
any other items that require discussion / explanation in the summary.
5.2.6 INSTRUMENT CALIBRATION CERTIFICATES
Report shall contain a summary list of all instrumentation and equipment used on the project
accompanied by copies of the current calibration certificates.
Shall Data:
Instrument type
Instrument manufacturer and model number
Instrument serial number
Instrument calibration date
5.2.7 ABBREVIATIONS
This section SHALL include a listing of all abbreviations and their definitions used in the report. As an
alternative, all abbreviations used in the report shall be defined in the body of the report.
5.3 AIRFLOW VELOCITY AND UNIFORMITY TEST FILTER FACE

AIRFLOW VELOCITY UNIDIRECTIONAL (Section 10.3)
Shall Data:
Technician Name
Test Date(s)
Instrument Identification
Sample Location Documentation
Room Identification Name / Number
As Left Data: Average airflow velocity
Test Results Data
Report all airflow measurements with corresponding grid locations.
Relative Standard Deviation when 6 or more readings are taken.
Identify all performance data that exceeds the acceptance criteria as specified in the contract
documents or as agreed to between the Owner / Buyer and the NEBB Certified CPT Firm.
27
SECTION 5
May Data:
Filter Size
Owner defined requirements
As Found Data
Test Occupancy State

Client Name

AIRFLOW VELOCITY NON-UNIDIRECTIONAL (Volume Method) (Section
10.4)
Shall Data:
Technician Name
Test Date(s)
Standard Operating Procedure
As Left Data: Calculated Average airflow velocity
Developed correction factor
Test Results Data
May Data:
Filter Size
As Found Data

Client Name
5.5 AIRFLOW VELOCITY AND UNIFORMITY TEST - FILTER FACE

AIRFLOW VELOCITY - NON-UNIDIRECTIONAL (Velocity Method) (Section
10.5)
Shall Data:
Technician Name
Test Date(s)
As Left Data: Average airflow velocity
Test Results Data
Relative Standard Deviation
28
SECTION 5
May Data:
Filter Size
As Found Data

Client Name
5.6 AIRFLOW VELOCITY AND UNIFORMITY TEST AVERAGE ROOM

AIRFLOW VELOCITY (Section 10.6)
Shall Data:
Technician Name
Test Date(s)
As Left Data: Minimum airflow velocity
Maximum airflow velocity
Average airflow velocity
Test Results Data
May Data:
Filter Size
As Found Data

Client Name
5.7 AIRFLOW VOLUME AND UNIFORMITY TESTS FLOWHOOD METHOD

(Section 10.8)
Shall Data:
Technician Name
Test Date(s)
As Left Data: Average airflow volume
Test Results Data
29
SECTION 5
May Data:
Filter Size
As Found Data

Client Name
5.8 AIRFLOW VOLUME AND UNIFORMITY TESTS TRAVERSE METHOD

(Section 10.9)
Shall Data:
Technician Name
Test Date(s)
Duct Size and Individual Velocities
As Left Data: Total Airflow Volume
Test Results Data
May Data:
Filter Size
As Found Data

Client Name
5.9 FILTER INSTALLATION LEAK TESTS AEROSOL PHOTOMETER TEST

METHOD (Section 10.11)
Shall Data:
Technician Name
Test Date(s)
Challenge Medium
Upstream Challenge Concentration
Leak:
Location
Percent of Penetration
Type (Media, Grid, Gel, Etc.)
Test Results Data
30
Should Data:
Repairs (Existing): Number
Size
Location
Total Area
SECTION 5
Repairs (New): Number

Size
Location
Total Area
May Data:
As Found Data
Filter Size
Scan Rate
Repairs (Total): Total

Percent
of Repair
Area
Filter Pressure Drop

Client Name
5.10 FILTER INSTALLATION LEAK TESTS DISCRETE PARTICLE

COUNTER TEST METHOD (Section 10.12)
Shall Data:
Technician Name
Test Date(s)
Challenge Medium
Upstream Challenge Concentration / Particle Size
Leak:
Location
Type (Media, Grid, Gel, Etc.)
Test Results Data
Should Data:
Scan Rate
Repairs(Existing):Number
Size
Location
Total Area
Repairs (New): Number

Size
Location
Total Area
May Data:
Owner Defined Requirements
As Found Data
Filter Size
Repairs (Total):
Total Percent of Repair Area

Client Name
31
SECTION 5
5.11 FILTER INSTALLATION LEAK TESTS

PENETRATION TEST METHOD (Section 10.13)
TOTAL
AEROSOL
Shall Data:
Technician Name
Test Date(s)
Challenge Medium
Upstream Challenge Concentration
Percent of Overall Leak Penetration
Test Results Data
May Data:
As Found Data
Filter Size

Client Name
5.12 AIRBORNE PARTICLE COUNT CLEANLINESS CLASSIFICATION TEST

ISO STANDARD (NON-UNIDIRECTIONAL AND UNIDIRECTIONAL)
(Section 10.14)
Shall Data:
Technician Name
Test Date(s)
Test Results Data
Particle Size(s) of Interest
Actual Room Classification
May Data:
Client Name
32
SECTION 5
5.13 AIRBORNE PARTICLE COUNTING TESTS SEQUENTIAL SAMPLING

(Section 10.15)
Shall Data:
Technician Name
Test Date(s)
Test Results Data
Particle Size(s) of Interest
Actual Room Classification
May Data:
Client Name
5.14 ROOM PRESSURIZATION TESTS (SECTION 10.16)

Shall Data:
Technician Name
Test Date(s)
Test Results Data
May Data:
As Found Data
Client Name
Schematic diagram depicting direction of airflow and differential pressure magnitude
5.15 AIRFLOW PARALLELISM TESTS (Section 11.2)

Shall Data:
Technician Name
Test Date(s)
Test Results Data
Test Location Diagram
33
SECTION 5
May Data:
As Found Data
Client Name
5.16 RECOVERY TESTS (Section 11.3)

Shall Data:
Technician Name
Test Date(s)
Initial Particle Counts at Particle Size(s) of Interest
Challenge Medium
Challenge Concentration
Test Results Data:
Recovery Time
Ending Particle Count at Particle Size(s) of Interest
May Data:
As Found Data
Client Name
5.17 LIGHTING LEVEL AND UNIFORMITY TESTS (Section 11.4)

Shall Data:
Technician Name
Test Date(s)
Test Results Data
May Data:
Lighting Type(s)
Detail natural/artificial influences

Client Name
34
SECTION 5
5.18 SOUND LEVEL TESTS (Section 11.5)

Shall Data:
Technician Name
Test Date(s)
Test Results Data: Operating Sound Pressure Levels: NC Curve, RC Curve or A-Weighted Value
May Data:
Client Name
5.19 VIBRATION LEVEL TESTS (Section 11.6)

Shall Data:
Technician Name
Test Date(s)
Test Results Data: (data stated in appropriate units (SI or IP) and reported in terms of displacement,
velocity, acceleration and / or frequency based on scope requirements)
May Data:
Client Name
5.20 GENERAL TEMPERATURE AND HUMIDITY UNIFORMITY TESTS

(Section 11.8)
Shall Data:
Technician Name
Test Date(s)
Test Results Data
35
SECTION 5
May Data:
Client Name
Work Height Level
5.21 COMPREHENSIVE TEMPERATURE AND HUMIDITY UNIFORMITY

TESTS (Section 11.9)
Shall Data:
Technician Name
Test Date(s)
Work Height Level
Test Results Data
May Data:
Client Name
5.22 ELECTROSTATIC TESTS (Section 11.10)

Shall Data:
Technician Name
Test Date(s)
Test Parameters
Test Results Data
May Data:
Client Name
36
SECTION 5
5.23 CONDUCTIVITY TESTS (Section 11.11)

Shall Data:
Technician Name
Test Date(s)
Test Parameters
Test Results Data
May Data:
Client Name
5.24 ELECTROMAGNETIC INTERFERENCE (EMI) TEST

(Section 11.12)
Shall Data:
Technician Name
Test Date(s)
Test Parameters
Test Results Data
May Data:
Client Name
5.25 AIR CHANGE RATE (ACH) TEST (Section 11.13)

Shall Data:
Technician Name
Test Date(s)
Test Results Data
Identify all performance data that exceeds the acceptance criteria as specified herein or as agreed to
between the Owner / Buyer and the NEBB Certified CPT Firm.
37
SECTION 5
May Data:
Client Name
5.26 BENCH SCAN FILTER LEAK TESTS (Section 11.14)

Shall Data:
Technician Name
Test Date(s)
Challenge Medium
Upstream Challenge Concentration / Particle Size
Leak:
Location
Type (Media, Frame, Etc.)
Test Results Data
Should Data:
Scan Rate
Repairs: Number
Size
Location
Total Area
Total Percent of Media Area Repair
May Data:
Owner Defined Requirements
Filter Size
Client Name
38
PART 2 - PROCEDURES
SECTION 6 - CLEANROOM
STANDARD OPERATING
PROCEDURES
6.1 INTRODUCTION
The purpose of this Section is to provide an overview of Standard Operating Procedures (SOPs) for
the NEBB Certified CPT Firm. The NEBB Certified CPT Professional shall develop these SOPs and
shall be responsible for implementing them within the NEBB Certified CPT Firm.
The NEBB Certified CPT Firm shall have SOPs for the following areas:
a.
b.
c.
d.
e.
f.
Safety
Instrument Calibration
Technician Training
Cleanroom Test Procedures
Cleanroom Reports
Cleanroom Protocol
The NEBB Cleanroom program does not dictate the requirements of each SOP. That is up to each
NEBB Certified CPT Firm and NEBB Certified CPT Professional. This section will address the elements
that are included in writing and executing SOPs.
6.2 STANDARD OPERATING PROCEDURES

6.2.1 DESCRIPTION
Standard Operating Procedures (SOPs) are documents that describe internal procedures and how to
perform various routine operations. They contain step-by-step instructions that technicians consult in
order to maintain consistency in their test procedures, repeatability in their results and their reports.
SOPs are, in essence, written commitments that describe the performance of routine tasks.
6.2.2 FORMAT
There are many ways to format an SOP. When developing a format, it is important to consider the
various categories:
a.
b.
c.
d.
Title
Purpose
Scope
Responsibility
39
e.
f.
g.
h.
i.
j.
k.
l.
m.
n.
SECTION 6
CLEANROOM STANDARD
OPERATING PROCEDURES
References
Applicable Documents
Safety Considerations
Procedural Principles
Preliminary Operations
Procedures
Equipment and Instrumentation
Tools
Calculations
Documentation Requirements
6.2.3 TITLE
The Title of an SOP should be direct and brief, describing each procedure in a way that identifies its
purpose. The Title should also include any key words useful for locating the procedure in a list of
SOPs. Titles should be used to group SOPs by purpose, test method, etc.
6.2.4 PURPOSE
The Purpose of an SOP often restates a well-written SOP title, but can also be used to expand upon
the purpose of the procedure.
6.2.5 SCOPE
The Scope describes the application of the SOP. To define the Scope of an SOP, the NEBB Certified
CPT Professional should consider to what and to whom the procedure applies, and when it is to be
applied.
6.2.6 RESPONSIBILITY
The SOP defines who is responsible for performing the operations cited. For example, it might cite a
department or mandate specific training requirements for individuals within a department. SOPs also
support routine regulated operations. SOPs should be written by the NEBB Certified CPT
Professional in conjunction with the individuals who perform the operations. Although particular
individuals in each department may write the majority of the procedures, it is important that everyone
in the NEBB Certified CPT Firm be trained to draft and review SOPs.
6.2.7 REFERENCES AND DOCUMENTS
The References and Applicable Documents sections of an SOP are optional. These sections can be
used to reference allied SOPs, standards, protocols, or additional information sources, such as
vendor manuals and instruction booklets.
6.2.8 SAFETY
Safety considerations appear in all appropriate SOPs. These include physical safety issues (such as
hard hats and appropriate eye protection), biological contamination issues (such as masks, gloves
and biological safety cabinets) and chemical hazards. It should also include any environmental issues
and the appropriate response that should occur during the execution of a procedure.
6.2.9 PROCEDURAL PRINCIPLES
Procedural Principles are provided to help technicians and reviewers understand the fundamental
principles of the SOP. This section should also be used to explain why the procedure is required in
the context of the facility operations.
40
SECTION 6
CLEANROOM STANDARD
6.2.10 PRELIMINARY OPERATIONS

Preliminary Operations are another optional section of an SOP. It may include any operations that
should be completed before the actual procedure is initiated. For example, there may be a need to
calibrate equipment before the procedure begins. In addition, some facilities require a material
checklist section to ensure that all materials required to complete the work are available before the
work begins.
6.2.11 PROCEDURES
Procedures should be simple, direct, step-by-step narratives that explain how to perform the tasks in a
manner that supports the execution. Any sampling or testing that might occur to support the task
should also be cited. The Procedure should include diagrams and drawings in this section when they
facilitate understanding of the instructions.
6.2.12 TOOLS
The SOP should contain a listing of all required tools and instrumentation required to perform the
required task(s).
6.2.13 CALCULATIONS
Calculations of a final result must also appear in appropriate SOPs. The calculations should include
all equations, conversion factors, constants, etc. The SOP Procedure shall detail how to calculate the
final results; however, generally it should not dictate acceptance criteria for that result.
6.2.14 DOCUMENTATION REQUIREMENTS
Documentation Requirements for an SOP should address any standard forms to be completed during
the procedure. This section should address distribution of results, if applicable. Procedural deviation
documentation requirements should also be outlined or referenced in this section.
Each page of an SOP document should contain its abbreviated title, SOP number; edition number and
pagination. The company name and some declaration of confidentiality can also appear on each
page. As long as each page contains the SOP number and its edition number, only one page
usually the firstneeds to contain the document approval signatures and the date of approval.
6.3 ADDITIONAL SOP REQUIREMENTS

6.3.1 LANGUAGE AND DETAIL
The NEBB Certified CPT Professional should write SOPs for the technicians who will use them on a
daily basis. Use clear and direct language. Use active verbs for procedural directives. SOPs must
be specific enough to be clear and accurate, yet flexible enough to be useful.
When citing the use of an item in a procedure, name the item and its model number. Slang terms for
equipment, departments, or procedures may be used, as long as they are explained somewhere in
the text to ensure clarity for an outside reviewer. It is good policy for draft SOPs to be reviewed by
the technicians who will use them.
6.3.2 REVIEW AND APPROVAL
The review and approval process shall be executed by two distinct individuals: the author and the
reviewer. Both individuals shall sign the document. The author should sign first and the reviewer
should then second. The reviewer shall be a person who can knowledgeably review and approve the
procedure.
41
SECTION 6
CLEANROOM STANDARD
6.3.3 DISTRIBUTION AND CONTROL

The distribution of approved SOPs must be controlled. Each department shall maintain a master set
of procedures with all distribution(s) documented. There are several ways to document these events
such as with log books or forms. Whatever the system, the NEBB Certified CPT Professional and the
NEBB Certified CPT Firm shall be able to track the history of creation, change, distribution and use of
each document.
6.3.4 MODIFICATIONS
When revised procedures are issued, it shall be documented that the previous versions of the
procedure are retrieved and destroyed. The NEBB Certified CPT Professional and the NEBB
Certified CPT Firm shall be able to track the history, change, distribution and use of each document.
6.3.5 DATA COLLECTION FORMS / REPORTS
Data collection shall be in accordance with the requirements of Section 5 for all primary and
secondary cleanroom performance tests identified in Sections 10 and 11. If unique or non-standard
procedures are required for a project, data should be collected and documented in a manner similar to
the requirements of this Procedural Standard.
42
SECTION 7 CLEANROOM
SAFETY
7.1 INTRODUCTION
A health and safety program is a definite plan of action designed to prevent accidents and
occupational diseases. A health and safety program should include the elements required by the
health and safety legislation as a minimum. This section summarizes the general elements of a
health and safety program. This should help NEBB Firms to develop programs to deal with their
specific needs. Because many small and medium-sized enterprises lack the resources of larger
organizations, it is even more vital that small and medium-sized enterprises involve all employees in
health and safety activities. The more comprehensive the program is, the more employee
involvement can be expected.
The health and safety program discussed in this section is a guideline. The project specific safety
program shall be as specified in the contract documents or as agreed to between the Owner / Buyer
Most often the NEBB Certified CPT Firm will be required to follow the client project specific safety
program; however in the absence of this project specific safety program, the firms SOP for cleanroom
health and safety program shall be followed. For this reason, the NEBB Certified CPT Firm shall have
a Standard Operating Procedures (SOP) for Health and Safety.
7.2 DESIGNING A HEALTH AND SAFETY PROGRAM

7.2.1 DESIGNING A PROGRAM POLICY
A NEBB Certified CPT Firms health and safety policy is a statement of principles and general rules
that serve as guides for action.
The policy should mention:
a.
b.
c.
d.
e.
f.
g.
Management's commitment to protect the safety and health of employees

The objectives of the program
The organization's basic health and safety philosophy
Who is accountable for health and safety programs
The general responsibilities of all employees
That health and safety shall not be sacrificed for expediency
That unacceptable performance of health and safety conduct will not be tolerated
The policy should be:

a.
b.
c.
d.
e.
Stated in clear, unambiguous, and unequivocal terms

Signed by the incumbent chief executive officer
Kept up-to-date
Communicated to each employee
Adhered to in all work activities
43
SECTION 7
CLEANROOM SAFETY
7.2.2 DESIGNING A TRAINING PROGRAM

The objective of training is to ease the implementation of health and safety policies into specific job
practices and to raise awareness and skill levels of a technician to an acceptable standard.
Occasions when employee training should be required are:
a.
b.
c.
d.
e.
Commencement of employment
Reassignment or transfer to a new job
Introduction of new equipment, processes, or procedures
Inadequate performance
Customer and job site related chemical or biological hazards, equipment, processes, or
procedures
The NEBB Certified CPT Firm should have the following topics included in the safety training:
a.
b.
c.
d.
e.
f.
g.
h.
i.
j.
k.
l.
Safety and the Professional

Know your accident problems
Human relations
Maintaining interest in safety
Instructing for safety
Industrial hygiene
Personal protective equipment
Industrial housekeeping
Material handling and storage
Guarding machines and mechanisms
Hand and portable power tools
Fire protection
7.2.3 ESSENTIALS OF THE HEALTH AND SAFETY PROGRAM

While different NEBB Certified CPT Firms will have different needs and scope for specific elements
required in their health and safety program, the following basic items may be considered in each case:
a.
b.
c.
d.
e.
f.
g.
h.
i.
j.
k.
l.
Individual responsibility
Occupational health and / or safety representative
Health and safety rules
Correct work procedures
Employee orientation
Training
Workplace inspections
Reporting and investigating accidents
Emergency procedures
Medical and first aid
Health and safety incentives
Workplace specific items
7.3 RESPONSIBILITIES
7.3.1 INDIVIDUAL HEALTH AND SAFETY RESPONSIBILITIES
Health and safety is the joint responsibility of management and workers. All health and safety
activities are based on specific individual responsibilities. Responsibility may be defined as an
44
SECTION 7
CLEANROOM SAFETY
individual's obligation to carry out assigned duties. Authority implies the right to make decisions and
the power to direct others.
7.3.2 NEBB CERTIFIED CPT PROFESSIONAL RESPONSIBILITIES
To fulfill their responsibilities, the NEBB Certified CPT Professional should:
a.
b.
c.
d.
e.
f.
g.
h.
i.
j.
k.
l.
m.
n.
o.
p.
q.
r.
s.
t.
u.
Instruct workers to follow safe work practices

Enforce health and safety regulations
Correct unsafe acts and unsafe conditions
Ensure that only authorized, adequately trained workers operate equipment
Report and investigate all accidents / incidents
Inspect own area and taking remedial action to minimize or eliminate hazards
Ensure that equipment is properly maintained
Promote safety awareness in workers
Provide a safe and healthful workplace
Establish and maintain a health and safety program
Ensure that workers are trained or certified, as required
Report accidents and cases of occupational disease to the appropriate authority
Provide medical and first aid facilities
Ensure that personal protective equipment is available
Provide workers with health and safety information
Evaluate health and safety performance of Cleanroom technicians
Advise all employees on health and safety matters
Coordinate interdepartmental health and safety activities
Provide health and safety training
Conduct research on special problems
Attend health and safety committee meetings as a resource person
7.3.3 FIELD TECHNICIAN RESPONSIBILITIES

To fulfill their responsibilities, the field technicians should:
a.
b.
c.
d.
e.
f.
g.
h.
i.
Use personal protection and safety equipment as required by the Employer

Follow safe work procedures
Know and comply with all regulations
Report any injury or illness immediately
Report unsafe acts and unsafe conditions
Participate in joint health and safety committees
Know what these responsibilities are (communication required)
Have sufficient authority to carry them out (organizational issue)
Have the required ability and competence (training or certification required)
7.4 ELEMENTS OF THE PROGRAM

The NEBB Certified CPT Professional should address the following elements of the NEBB Certified
CPT Firms health and safety program:
a.
b.
c.
d.
Establish work procedures

Analyze project hazards
Establish guideline rules
Conduct employee safety orientation
45
e.
f.
g.
h.
i.
j.
k.
SECTION 7
CLEANROOM SAFETY
Establish emergency procedures

Establish medical and first aid action plan
Perform routine project site safety audits
Complete project accident / injury reports
Investigate project accidents / injuries
Establish and enforce return-to-work policy
Promote employee involvement in health and safety programs
7.4.1 PROJECT SPECIFIC ITEMS

Examples of project specific items that should be included in health and safety programs are:
a.
b.
c.
d.
e.
f.
g.
h.
Material Safety Data Sheets (MSDS)

Lock out procedures
Chemical handling rules
Biological material handling rules
Personal hygiene
Vehicle safety rules
Working alone guidelines
Personal protective equipment requirements
7.4.2 HEALTH AND SAFETY PROGRAM IMPLEMENTATION

A good health and safety program provides a clear set of guidelines for activities that, if followed, will
reduce accidents and cases of occupational disease. A NEBB Certified CPT Professional should
demonstrate commitment and support the program by:
a. Providing resources such as time, money, and personnel
b. Ensuring that employees receive training or certification as required
c. Making all applicable health and safety information available to all employees entitled to
receive it
d. Including health and safety performance as part of employee performances appraisals at all
levels
e. Attending health and safety meetings
f. The program must be communicated to all employees, special emphasis should be given to
new technicians and newly approved NEBB Certified CPT Professionals.
g. Revisions to policies and procedures should be publicized.
h. The program should be available in a single written document. (However, if separate manuals
have been developed for various elements, such as accident investigation procedures, their
use should be referenced in the main document).
46
SECTION 8 CLEANROOM
PROTOCOL
8.1 INTRODUCTION
The purpose of this Section is to provide an overview of the cleanroom protocol procedures that
should be observed in performing the various cleanroom tests. In general, there are protocols and
procedures for cleanroom entry, garment control, tool and equipment entry and gowning procedures. In
addition to entry protocols, there are also protocols and behavior requirements while in the cleanroom.
The protocols suggested in this section are guidelines and the final procedures shall be as specified in
the contract documents or as agreed to between the Owner / Buyer and the NEBB Certified CPT Firm.
The NEBB Certified CPT Firm shall be responsible for creating their own cleanroom protocol and
develop it into a Standard Operating Procedure (SOP) for their firm. Most often the NEBB Certified
CPT Firm will be required to follow the client project specific protocol. However in the absence of this
project specific protocol, the firms SOP for cleanroom protocol shall be followed. At a minimum, the
NEBB Certified CPT Firms SOP for Cleanroom Protocol should cover: gowning procedures,
equipment entrance procedures, and guidelines for employee conduct.
8.2 CLEANROOM PROCEDURES

8.2.1 GOWNING PROCEDURES
The processes and operations that occur in a cleanroom are unique to that particular owner and facility.
Therefore the gowning procedures may vary to some degree between each cleanroom and each owner.
It is imperative that the Facility / Owners SOP be reviewed for the specific gowning procedure. When it
exists, the Owners SOP always takes precedence and must be followed.
In many cleanroom gowning facilities there are two distinct zones in the gowning area. In some
facilities, the two distinct zones may exist in the same room / space defined by some imaginary
boundary. The initial area will have gloves, hair bonnets and shoe covers. Since the outside surface of
the cleanroom garments should be kept as clean as possible, care should be used to avoid touching
the outside of the garment with bare hands, hair and street shoes. This is accomplished by donning
gloves, bouffant head covers and shoe covers before entering the second phase of the gowning area.
It is important to note that cleanrooms in the electronics industry may be quite different from cleanrooms
in the pharmaceutical and bio-technology industries. While gowning remains important, a high
emphasis is placed on sterility. Cleaning / washing procedures can be much more rigorous. In some
instances, usually associated with bio-containment spaces (i.e. BSL3 and BSL4 labs), street clothes will
not be allowed into the room and a complete change of clothing is required.
Upon entering the second area it is important to note that different gowning garments may be used in
different facilities. Since gowning materials differ, there is no hard and fast method that can be outlined
for actual gowning. Typically, gowning should be done from the head down. Therefore the hood is to be
donned first followed by the garment and then the foot covers. Once the garment is obtained, care
should be taken to avoid contaminating the exterior surface with the interior of the garment. Proper
garment sizing is also required. Once obtained, the garment user should never allow the garment to
touch or drag on the floor.
47
SECTION 8
CLEANROOM PROTOCOL
8.2.2 EQUIPMENT ENTRANCE PROCEDURES

Tools, instrumentation and equipment also require special preparation before they can be brought into a
cleanroom. As with gowning, each facility will have their own methods and requirements for introducing
these items into a cleanroom. It is imperative that the Facility / Owners SOP be reviewed for material
ingress to their cleanroom. When it exists, the Owners SOP always takes precedence and must be
followed.
Typically, there will be a wipe-down station for anything entering the cleanroom. There will also be a
wipe-down procedure. Often the procedure will involve wiping down the instruments with noncontaminating wipes moistened with de-ionized water and isopropyl alcohol (IPA) or other sterile
solvents. The ingress for equipment may be a separate entrance from the gowning entrance.
8.2.3 CLEANROOM CONDUCT
Examples of personnel rules used by cleanroom operators may be:
a.
b.
c.
d.
e.
f.
g.
h.
i.
j.
k.
Clean hands and face before entering clean areas

Use lotions and soap containing lanolin to reduce skin flaking
Avoid skin contact with solvents
Wearing cosmetics and skin medications may not be permitted
Jewelry may not be permitted
Tobacco use, eating and drinking is not permitted
Required gowning, masks, gloves and shoe covers to be worn at all times
Equipment, instruments and materials should be cleaned before entry
Non-shedding paper and pens should be used. Pencils and erasers are not permitted
Work parts are to be handled only with gloved hands, tweezers, or other methods to avoid
transfer of skin particles and oils
Use containers to transfer and/or store materials
48
SECTION 9 CLEANROOM TESTS

9.1 INTRODUCTION
This section provides an overview of all cleanroom tests. The procedures required to perform these
tests are described in Sections 10 and 11. Certification tests and procedures may vary considerably
from project to project. The choice of certification tests may be based on the cleanliness class level,
type of cleanroom airflow, occupancy mode and the product produced. The scope of the cleanroom
testing services may vary based on the contract document requirements, or based on the agreed scope
of services between the Owner / Buyer and the NEBB Certified CPT Firm. Table 9-1, extrapolated from
the current version of IEST-RP-CC006, lists recommended tests for initial cleanroom certification.
9.2 CLEANROOM AIRFLOWS

Table 9-1 lists cleanroom certification tests by the type of cleanroom design, unidirectional airflow, nonunidirectional airflow and mixed airflow.
9.2.1 UNIDIRECTIONAL AIRFLOW
In a unidirectional airflow system, air is uniformly introduced through HEPA filters from one entire
surface of the room, such as the ceiling or a wall. For unidirectional airflow, the filter coverage must be
at least 80% coverage. The air flows perpendicularly from this surface at a constant velocity and is
removed at the opposite surface (wall or floor). Unidirectional flow provides a direct, predictable path
that a sub-micrometer size particle will follow through the cleanroom, with the minimum opportunity for
contaminating room components. It also captures the particles constantly generated within the room
and introduced into the airstream, thereby reducing the potential for cross-contamination.
9.2.2 NON-UNIDIRECTIONAL AIRFLOW
In a non-unidirectional airflow system, air is supplied to the cleanroom conventionally through HEPA
filters in a random airflow pattern and mixes with internal air by induction.
9.2.3 MIXED AIRFLOW
A mixed airflow system may be used in a cleanroom with two (or more) areas requiring different
classifications. Non-unidirectional airflow and unidirectional airflow will sometimes exist in the same
space and may be classified independently.
9.3 OCCUPANCY MODE

Cleanroom certification tests are performed after a new cleanroom is built and then periodically as
determined by the cleanroom operator or owner. The three occupancy modes are: As-Built, At-Rest
and Operational. These three occupancy modes affect some of the test procedures and are useful in
specifying testing and acceptance criteria for cleanrooms.
For new cleanroom construction projects, testing is normally done in the As-Built occupancy mode.
Testing of existing cleanrooms is usually performed with the facility in the At-Rest or Operational
occupancy modes. The occupancy mode shall be as specified in the contract documents or as mutually
agreed to between the Owner / Buyer and the NEBB Certified CPT Firm.
49
SECTION 9
CLEANROOM TESTS
9.3.1 AS-BUILT FACILITY

An As-Built facility is a cleanroom which is complete and operating, with all services connected and
functioning, but has no production equipment or operating personnel within the facility.
9.3.2 AT-REST FACILITY
An At-Rest facility is a cleanroom which is complete and has the production equipment installed and
operating, but has no personnel within the facility.
9.3.3 OPERATIONAL FACILITY
An Operational facility is a cleanroom in normal operation, including production equipment installed and
operating under normal conditions with all operating personnel present.
9.3.4 EXCEPTIONS
In many instances, there will be deviations from these definitions. (Examples: a partial installation of
process equipment may have been installed and may or may not be operating; process equipment
exhausts may or may not be operating.) These situations should be recognized and noted by the
NEBB Certified CPT Firm on any affected test requirements.
9.4 REFERENCE DOCUMENTS

Cleanliness classifications are defined by ISO Standard 14644, Parts 1, 2 and 3. The NEBB Certified
CPT Professional shall have a thorough knowledge of these ISO Standards.
In addition, procedures for performing for CPT tests are identified in the following IEST publications:
RP-CC006 and RP-CC034
The NEBB Certified CPT Firm Shall possess current copies of the above referenced standards and
publications in addition to the NEBB Procedural Standards for Certified Testing of Cleanrooms.
Other national and international standards also exist which the NEBB Certified CPT Professional may
need to access. (See Appendix B)
9.5 PRIMARY TESTS

The primary tests are related to airborne particulate cleanliness classes as required by ISO 14644. In
general, the primary tests should be performed in the order that will be most beneficial to the project being
certified. By performing these tests, the cleanroom will be correctly classified to the appropriate class level.
These tests include:
a. Airflow Velocity and Uniformity Tests
b. Airflow Volume and Uniformity Tests
c. HEPA Filter Installation Leak Tests
d. Airborne Particle Count Cleanliness Classification Tests
e. Room Pressurization Tests
9.6 SECONDARY TESTS

The secondary tests are user optional and relate to particle, air movement and ancillary systems within
the cleanroom. These tests include:
50
SECTION 9
CLEANROOM TESTS
a. Airflow Parallelism Tests

b. Recovery Tests
c. Lighting Level and Uniformity Tests
d. Sound Level Tests
e. Vibration Level Tests
f. Temperature and Humidity Uniformity Tests.
g. Electrostatic Tests
h. Conductivity Tests
i. Electromagnetic Interference (EMI) Test
j. Air Change Rate (ACH) Test
k. Bench Scan Filter Leak Tests
9.7 TESTING INTERVALS

Table 9-1 contains Recommended Tests by Cleanroom Type. Table 9-2 contains Recommended
Testing Intervals for each of the various primary and secondary cleanroom performance tests.
51
SECTION 9
CLEANROOM TESTS
TABLE 9-1 Recommended Tests by Cleanroom Type*

NEBB
Procedural
Standards
Section Test
Unidirectional
Airflow
NonUnidirectional
Airflow
Mixed
Airflow
IEST
Section
10
Airflow volume
& uniformity
1,2,3
1,2,3
1,2,3
6.1
10
Airflow velocity
& uniformity
1,2,3
1,2,3
1,2,3
6.1
10
Filter leak
1,2
1,2
1,2
6.2
10
Particle count
1,2,3
1,2,3
1,2,3
6.3
10
Pressurization
1,2,3
1,2,3
1,2,3
6.4
11
Parallelism
1,2
Not Applicable
1,2,3
6.5
11
Recovery
1,2
1,2
1,2
6.7
11
Lighting level
1,2,3
1,2,3
1,2,3
6.9
11
Sound level
1,2,3
1,2,3
1,2,3
6.10
11
Temperature
and
Humidity
uniformity
1,2,3
1,2,3
1,2,3
6.11 6.13
11
Vibration level
1,2,3
1,2,3
1,2,3
6.14
11
Electrostatic
1,2,3
1,2,3
1,2,3
11
Conductivity
1,2,3
1,2,3
1,2,3
1,2,3
1,2,3
1,2,3
Electromagnetic
11
Interference
(EMI)
11
Air Change
Rate
1,2,3
1,2,3
1,2,3
11
Bench Scan
The order in which tests are performed is optional, but some sequences are optimal.
1: Test is suited to As-Built occupancy mode
2: Test is suited to At-Rest occupancy mode
3: Test is suited to Operational occupancy mode
4: These tests are not defined in IEST-RP-CC006
*Most material extrapolated from IEST-RP-CC006
52
SECTION 9
CLEANROOM TESTS
TABLE 9-2 Recommended Testing Intervals

NEBB Procedural
Standards Section
ISO Reference
Test
NEBB Recommended
Test Interval (Months)
IEST
Section
10
ISO 14644-3: B.4
Airflow volume & uniformity

Airflow velocity & uniformity
12
6.1
10
ISO 14644-3: B.6
Filter leak
12
6.2
10
Annex B, ISO
14644-1
Particle count
ISO Class 5
6.3
10
Annex B, ISO
14644-1
Particle count
12
6.3
10
ISO 14644-3: B.5
Pressurization
12
6.4
11
ISO 14644-3: B.7
Parallelism
12
6.5
11
ISO 14644-3:
B.13
Recovery
24
6.7
11
N/A
Lighting level
24
6.9
11
N/A
Sound level
24
6.10
ISO 14644-3: B.9

ISO 14644-3:10
Temperature and
Humidity Uniformity
12
6.11 6.13
11
N/A
Vibration level
24
6.14
11
ISO 14644-3:
B.11
Electrostatic
24
N/A
11
N/A
Conductivity
24
N/A
11
N/A
24
N/A
11
N/A
Air Change Rate
12
N/A
11
N/A
Bench Scan
N/A
N/A
11
> ISO Class 5
Electromagnetic
Interference (EMI)
N/A: Not Applicable
53
SECTION 9
CLEANROOM TESTS
54
SECTION 10 PRIMARY TESTS

10.1 INTRODUCTION
The primary tests measure attributes that contribute to success of particle control. A thorough operation
performance evaluation employing these tests will assist in identifying the current cleanliness
classification. In general, the primary tests should be performed in the order that will be most beneficial
to the project being certified.
The primary tests include:
a.
b.
c.
d.
e.
Airflow Velocity and Uniformity Tests

Airflow Volume and Uniformity Tests
Filter Installation Leak Tests
Airborne Particle Count Cleanliness Classification Tests
Room Pressurization Tests
Whenever the term filter is used in this section, it is to be implied that the meaning pertains to both
HEPA and ULPA filters.
10.2 CLEANROOM / FILTER AIRFLOW VELOCITY AND UNIFORMITY TESTS

These tests are performed to determine the average filter face velocity and uniformity, and / or the
average room airflow velocity and uniformity within a cleanroom.
Airflow velocity in meters per second (m/s) or feet per minute (fpm) is a measurement of the speed of
the airflow. An average velocity is calculated by dividing the cleanroom / filter area into equal grids and
taking the airflow velocity in the center of each of these grids. The average airflow velocity is calculated
by dividing the total of the airflow grid velocities by the number of readings taken.
The location of the airflow reading in the work zone shall either be as specified in the contract
documents or as agreed to between the Owner / Buyer and the NEBB Certified CPT Firm. For filter
face airflow velocity, the tests normally are performed at a specified distance from the filter face: 75
mm, 150 mm, or 300 mm (3, 6, or 12). For room airflow velocity, the tests are normally performed at
the specified work surface elevation. Typically this is 0.91 m (36) above the floor. In order to eliminate
confusion of the testing procedures, the tests shall be titled: Filter Face Airflow Velocity Tests or Room
Airflow Velocity Tests. Although the actual test procedures are basically the same for each test, it is
necessary to differentiate between each procedure.

AIRFLOW VELOCITY UNIDIRECTIONAL
The purpose of the filter face airflow velocity test is to document the average airflow velocity and
uniformity of the filter face in unidirectional airflow.
10.3.1 INSTRUMENTATION AND EQUIPMENT
An airflow velocity instrument that conforms to the requirements of Table 4-1.
55
SECTION 10
PRIMARY TESTS
10.3.2 TEST PROCEDURES

10.3.2.1 Measurement readings shall be taken at a distance from the face of the filter system, as
specified in the contract documents or as agreed to between the Owner / Buyer and the NEBB Certified
CPT Firm.
10.3.2.2 The measurement area shall be a cross-sectional area of the filter face normal to the airflow.
This area shall consist of the net effective filter media area, which is exclusive of the filter frame. For
example, a 610 mm x 1220 mm (24 inch x 48 inch) filter does not have a net effective area of 0.74
square meters (8.0 square feet), but is closer to approximately 0.66 square meters (7.1 square feet) with
the frame, media glue joints, etc., deducted.
10.3.2.3 When using a single point measurement instrument, such as a hot wire anemometer, divide the
net filter face into grids of equal area of not greater than 0.09 square meters (1.0 square foot). When
using a multi-point instrument, such as tube array, divide the net filter face into grids of equal area of not
greater than 0.37 square meters (4.0 square feet). The grid area shall be as specified in the contract
10.3.2.4 Measure and record the airflow velocity at each grid point 150 mm (6 in.) from the filter face or
as specified in the contract documents or as agreed to between the Owner and the NEBB Certified CPT
Firm. Special care is necessary to keep the sampled area unobstructed during the airflow
measurement. The use of a support stand is recommended with single point type measuring
instruments. The use of stand off legs of the appropriate length is recommended for a tube array.
10.3.2.5 Take the measurement for a minimum of 5 seconds or the instrument manufacturers minimum
specified time, using the average during that period as the measurement.
10.3.2.6 Calculate the Relative Standard Deviation (RSD). See Appendix C, Section C.6.4.
10.3.3 ACCEPTANCE
10.3.4.1 The average airflow velocity for the filter should be within 10% of that specified in the contract
10.3.4.2 The Relative Standard Deviation should not exceed 15% unless otherwise specified in the
contract documents or as agreed to between the Owner / Buyer and the NEBB Certified CPT Firm.
10.3.4 REPORTING
See Section 5.3 for reporting requirements.

AIRFLOW VELOCITY NON-UNIDIRECTIONAL (Volume Method)
For non-unidirectional airflow cleanrooms, the airflow volume measurements are preferable and are
more accurate for calculating airflow velocities when readings are taken at a distance greater than 150
mm (6 in.) from the filter face. If filter face airflow velocity measurement readings are performed utilizing
a direct reading flowhood, use the testing requirements identified for flowhood volume testing in Section
10.8 and as identified below.
When airflow volumes are being determined using the measured airflow velocities, it is necessary to
develop a correction factor that accounts for the instrument and filter measurement discrepancies that
may exist. See Appendix C, Section C.11.
56
SECTION 10
PRIMARY TESTS
10.4.1 INSTRUMENTION AND EQUIPMENT

A direct reading flowhood that conforms to the requirements of Table 4-1 in Section 4.
10.4.2.1 Flow measuring hoods are preferred for taking airflow volume measurements from each filter.
A flowhood with an appropriate flow meter is required.
10.4.2.2 Seat the flow measuring hood firmly to the filter frame to prevent air leakage.
10.4.2.3 The flowhood shall be adequately sized to capture all the air exiting the filter being tested.
10.4.2.4 Measure and record the airflow volumes of each filter in liters per second (L/s) or cubic feet
per minute (cfm).
10.4.3 ACCEPTANCE
10.4.3.1 Measure the total airflow for each filter. Determine the average filter face airflow velocity by
dividing the measured airflow by the net effective filter area.
10.4.3.2 The average airflow velocity of each filter for the cleanroom should be within 10% of that
CPT Firm.
10.4.4 REPORTING

AIRFLOW VELOCITY NON-UNIDIRECTIONAL (Velocity Method)
The purpose of the filter face airflow velocity test is to document the average airflow velocity and
uniformity of the filter face non-unidirectional airflow.
NEBB advises that a volumetric method be used to calculate the filter face velocity in a
non-unidirectional cleanroom, however when project specifications require a direct velocity
measurement, the following procedure should be used.
An airflow velocity instrument that conforms to the requirements of Table 4-1 in Section 4.
10.5.2.1 Measurement readings shall be taken at a distance from the face of the filter system, as
CPT Firm.
10.5.2.2 The measurement area shall be a cross-sectional area of the filter face normal to the airflow.
This area shall consist of the net effective filter media area, which is exclusive of the filter frame. For
example, a 600 mm x 1200 mm (24 inch x 48 inch) filter does not have a net effective area of 0.74
square meters (8.0 square feet), but is closer to approximately 0.66 square meters (7.1 square feet) with
the frame, media glue joints, etc., deducted.
57
SECTION 10
PRIMARY TESTS
10.5.2.3 When using a single point measurement instrument, such as a hot wire anemometer, divide the
net filter face into grids of equal area of not greater than 0.09 square meters (1.0 square foot). When
using a multi-point instrument, such as tube array, divide the net filter face into grids of equal area of not
greater than 0.37 square meters (4.0 square feet). The grid area shall be as specified in the contract
10.5.2.4 Measure and record the airflow velocity at each grid point 150 mm (6 in.) from the filter face or
as specified in the contract documents or as agreed to between the Owner and the NEBB Certified CPT
Firm. Special care is necessary to keep the sampled area unobstructed during the airflow
measurement. The use of a support stand is recommended with single point (hot wire) type measuring
instruments. The use of a support stand is recommended with single point type measuring instruments.
The use of stand off legs of the appropriate length is recommended for a tube array.
10.5.2.5 Take the measurement for a minimum of 5 seconds or the instrument manufacturers minimum
specified time, using the average during that period as the measurement.
10.5.3 ACCEPTANCE
10.5.3.1 The average airflow velocity for the cleanroom should be within 10% of that specified in the
10.5.3.2 The relative standard deviation should not exceed 15% unless otherwise specified in the
10.5.4 REPORTING
10.6 AIRFLOW VELOCITY AND UNIFORMITY TEST AVERAGE ROOM

AIRFLOW VELOCITY
The purpose of this test is to determine the average room airflow velocity and uniformity of that airflow
velocity at the specified work surface elevation.
10.6.1 INSTRUMENTS AND EQUIPMENT
An airflow velocity instrument that conforms to the requirements of Table 4-1.
10.6.2.1 Measurement readings shall be taken at specified planes and locations in the room as specified
in the contract documents or as agreed to between the Owner / Buyer and the NEBB Certified CPT
Firm.
10.6.2.2 The measurement area shall be a cross-sectional area of the room or work area normal to the
airflow. This area shall consist of the total work zone or room.
10.6.2.3 Divide the area plane at the measurement point into grids of equal area of not greater than 1.49
square meters (16 square feet), or as specified in the contract documents or as agreed to between the
Owner / Buyer and the NEBB Certified CPT Firm.
58
SECTION 10
PRIMARY TESTS
10.6.2.4 Measure and record the airflow velocity of each grid point. Special care is necessary to keep
the sampled area unobstructed during the airflow measurement. The use of a support stand may be
necessary with single point measuring (hot wire) instruments.
10.6.2.4 Take the measurement for a minimum of 5 seconds or the minimum specified time for the
meter, using the average during that period as the measurement.
10.6.3 ACCEPTANCE
10.6.3.1 The average airflow velocity for the cleanroom should be within 10% of that specified in the
10.6.3.2 The average or total airflow volume for the cleanroom should be within 10% of that specified
Firm.
10.6.4 REPORTING
10.7 AIRFLOW VOLUME AND UNIFORMITY TEST

The airflow volume in liters per second (L/s) or cubic feet per minute (cfm) is a measurement of the
airflow quantity. Airflow volumes may be measured by one of three methods; 1) using a direct reading
flowhood, 2) performing a total air traverse of each, or 3) measuring the airflow velocity of each filter and
then calculating the air volume of the filter. For accuracy and repeatability, the preferred method of
measuring airflow volume is with a direct reading flowhood. The traverse method is the most accurate
for normal HVAC TAB work, but this is not necessarily true for cleanrooms due to the duct inlet
conditions. Great care must be taken if the air volume is obtained by using the filter airflow velocity
because of the exit planes inaccuracies.
For non-unidirectional airflow cleanrooms, the airflow volume measurements are preferable and are
more accurate for calculating airflow velocities when the readings are taken at a distance greater than
150 mm (6 in.) from the filter face. As previously stated above, determining volume from filter face
velocities should only be done with a great deal of care due to the inaccuracies in calculating the exit
plane area. NEBB does NOT recommend determining airflow volumes by using airflow velocities in
non-unidirectional cleanrooms. There may be times when it is necessary to determine the filter airflow
volume using the filter airflow velocity method (when an obstruction prevents using a flowhood). The
procedures as identified in Section 10.3 and the appropriate correction factor should be followed to
determine the airflow volume. See Appendix C, Section C.11.
10.8 AIRFLOW VOLUME AND UNIFORMITY TEST FLOWHOOD METHOD

A direct reading flowhood that conforms to the requirements of Table 4-1.
59
SECTION 10
PRIMARY TESTS

10.8.2.1 Flow measuring hoods are preferred for taking airflow volume measurements from each filter or
supply air diffuser. The flowhood with an appropriate flow meter is required.
10.8.2.2 Seat the flow measuring hood firmly to the filter frame to prevent air leakage.
10.8.2.3 The flowhood shall be adequately sized to capture all the air exiting the filter being tested.
10.8.2.4 Measure and record the airflow volumes of each filter in liters per second (L/s) or cubic feet per
minute (cfm).
10.8.2.5 Calculate the Relative Standard Deviation (RSD).
necessary to calculate the (RSD).
See Appendix C for the requirements
10.8.3 ACCEPTANCE
10.8.3.1 The average airflow volume of each filter for the cleanroom should be within 10% of that
CPT Firm.
Firm.
10.8.4 REPORTING
10.9 AIRFLOW VOLUME AND UNIFORMITY TEST TRAVERSE METHOD

When the airflow volume cannot be measured using a flow hood then a total air traverse should be
employed. A suitable length of straight, hard duct is required for an accurate airflow velocity
measurement.
An airflow velocity instruments that conform to the requirements of Table 4-1.
Divide the traverse plane into grids of equal area. Record airflow velocity measurements in accordance
with the sample traverse layout. See Appendix C, Section C.5.1.
10.9.3 ACCEPTANCE
10.9.3.1 The average airflow volume of each filter for the cleanroom should be within 10% of that
CPT Firm.
Firm.
60
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10.9.4 REPORTING
10.10 FILTER INSTALLATION LEAK TESTS

The purpose of the filter installation integrity test is to ensure and confirm that the filter system is properly
installed by verifying the absence of bypass leakage in the installation, and that the filters are free of
defects and pinhole leaks.
The test is made by introducing an aerosol challenge upstream of the filters and scanning immediately
downstream of the filters and support frame. This procedure detects small pinholes or other damage in
the filter medium and frame seal, bypass leaks in the filter frame and gasket seal, and leaks in the filter
bank framework. For plenum ceilings, it may be necessary to also scan ceiling penetrations (i.e.
sprinkler heads, conduits, pipes, etc.) and ceiling joints.
Two different leak detection techniques are presented, along with recommendations for two different
aerosol challenge methods and two different detection instruments; 1) aerosol photometer test method
and 2) particle counter test method.
Another test method that is still sometimes referenced is identified as the Filter Installation Leak Tests
Ambient Challenge Test Method. This test is NOT recommended by NEBB. The reason that this test is
not recommended by NEBB is due to the low upstream particle concentrations normally found in recirculated air from cleanrooms. Typical users of this test are unable to locate significant leaks. Scan
rates are also quite excessive. See Appendix C, Section C.7.
10.10.1 LEAK TEST METHODS
For the above reasons, three methods of aerosol particle challenge tests are specified and used by
NEBB Certified CPT Firms:
a. Filter Installation Leak Tests Aerosol Photometer Test Method (Section 10.11)
b. Filter Installation Leak Tests Discrete Particle Counter Test Method (Section 10.12)
c. Filter Installation Leak Tests Total Aerosol Penetration Test Method (Section 10.13)
10.11 FILTER INSTALLATION LEAK TESTS AEROSOL PHOTOMETER

TEST METHOD
The photometer test method employs either logarithmic or linear mass concentration detection and does
not provide discrete quantitative analysis. This test is performed by introducing DOP, PAO or another
specified substitute aerosol upstream of filters and verifying the installations integrity by scanning the
downstream side of the filters with the photometer and appropriate probe.
10.11.1.1 A thermal or laskin nozzle generator that conforms to Table 4-1
10.11.1.2 Photometers that conform to the requirements of Table 4-1.
10.11.1.3 Scanning probe that conforms to the requirements of Table 4-1.
61
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10.11.2.1 Verify that the design airflow velocity has been balanced by a NEBB Certified TAB Firm prior
to performing the filter installation leak test.
10.11.2.2 Introduce the aerosol into the air supplied to the filters in a manner which will produce a
uniform challenge concentration at each of the filters being exposed at the same time. Where several, or
all, filters must be exposed simultaneously to the aerosol, it is recommended that the aerosol be
introduced at the blower inlet(s) or another location which will produce a uniform mixture over all of the
filters.
10.11.2.3 Measure the upstream concentration immediately upstream of the filter being tested. Care
must be exercised to assure that a uniform distribution of the challenge aerosol exists.
10.11.2.4 When using a Laskin nozzle aerosol generator set the air supply pressure at a minimum of
138 kPa (20 psi). Determine the amount of airflow volume being challenged. Using Equation 10-1,
calculate the quantity of Laskin nozzles required to achieve an upstream concentration level of 10 g/L
or greater, or as specified or as agreed to between the Owner / Buyer and the NEBB Certified CPT Firm.
Place the generator distribution tube in the location as determined in Section 10.11.2.2.
Equation 10-1 (SI): Required Number of Laskin Nozzles
N=
Where:
N
C
Q
Z
=
=
=
=
C Q
Z
Number of Laskin nozzles required

Required upstream challenge concentration (greater than 10 g/L)
Airflow volume being challenged (L/min)
Constant = 3823 x 100 = 382,300 L/min
Equation 10-1 (IP): Required Number of Laskin Nozzles
N=
Where:
N
C
Q
Z
=
=
=
=
C Q
Z
Number of Laskin nozzles required

Required upstream challenge concentration (greater than 10 g/L)
Airflow volume being challenged (cfm)
Constant = 135 x 100 = 13,500 cfm
The constant Z is based on one Laskin nozzle producing 100 g/L of challenge aerosol in 3820 L/min
(135 cfm) of airflow.
Note: When using more than one Laskin nozzle, the resulting aerosol generation may not be linear.
Caution should be exercised when determining the upstream challenge when using multiple Laskin
nozzles. It may be necessary to verify the actual concentration in mg/L with multiple Laskin nozzles
based on each aerosol generator. It is the NEBB Certified CPT Firms responsibility to verify output of
their aerosol generator.
10.11.2.5 When using a thermal generator operate per the manufacturers recommended operating
instructions.
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10.11.2.6 Measure the upstream aerosol challenge concentration, using either a linear or logarithmic
photometer scale.
10.11.2.7 Set the photometer to full scale (100%) and measure the upstream concentration. The
concentration should be established using one or more Laskin nozzles adjusted to produce an upstream
concentration of 10 to 20 micrograms per liter of aerosol.
10.11.2.8 Once the correct aerosol concentration is established, adjust the photometers gain such that
the concentration established represents 100% upstream concentration.
10.11.2.9 Increase the sensitivity of the photometer to a scale where 0.010% of the upstream
concentration can be easily read.
10.11.2.10 The filter face and the perimeter of the filter assembly shall be scanned by passing the probe
in slightly overlapping strokes so that the entire area of the filter is sampled. The probe shall be held
approximately 25 mm (1 inch) from the area to be tested during scanning. Separate passes shall be
made around the entire periphery of the filter, along the bond between the filter pack and the frame, and
around the seal between the filter and the device, at a scan rate of not more than 0.05 m/s or 5.0 cm/s
(10 fpm or 2 inches per second). This assumes an airflow filter face velocity of 0.46 to 0.56 m/s (90 to
110 fpm). If airflow filter face velocities are significantly different, the scan rate shall be calculated using
the information found in the current edition of IEST-RP-CC034, HEPA and ULPA Filter Leak Tests.
10.11.3 ACCEPTANCE
10.11.3.1 An unacceptable leak is defined as a sustained reading greater than 0.010% of the measured
upstream challenge concentration, or as specified in the contract documents or as agreed to between
10.11.4 REPORTING
See Section 5.9 for the reporting requirements.
10.11.5 REPAIRS
10.11.5.1 Filters may be repaired providing:
The size of the repair(s) is not greater than 3% of each filter face area. Additionally, a repair area
shall have a minimum dimension which shall not exceed 38 mm (1.5 inches) or as specified in the
10.11.5.2 Repairs to filter installation leaks may be made by procedures specified in the contract
10.12 FILTER INSTALLATION LEAK TESTS DISCRETE PARTICLE

COUNTER TEST METHOD
The particle counter test method employs discrete particle sizing and quantitative analysis. This test is
performed by introducing an artificial aerosol challenge upstream of the filters and verifying the
installations integrity by scanning the downstream side of the filters with the particle counter.
The challenge aerosol particle concentration must be greater than 3.53 x 107 (35,300,000) particles per
cubic meter, (3 x 106 [3,000,000] particles per cubic foot of air) based on using a probe that is 0.4 inches
in the direction of scan and at a scan rate of 2 inches per second. This concentration will allow a
63
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PRIMARY TESTS
reasonable scan rate that can be manually performed. Particle concentrations of 2.12 x 108
(212,000,000) particles per cubic meter, (6 x 106 [6,000,000] particles per cubic foot of air) are desirable
and will increase the accuracy with which leaks are detected.
NEBB recommends that this test be limited to cleanrooms where the cleanliness classification is ISO
Class 6 or cleaner.
10.12.1.1 A particle counter that conforms to the requirements of Table 4-1.
10.12.1.2 A hand held isokinetic sampling probe configured to provide adequate residence time while
scanning. Probe shall conform to the requirements of Table 4-1.
10.12.1.3 An aerosol particle generator as described in Table 4-1.
10.12.1.4 A diluter or a reduced flow rate particle counter that conforms to the requirements of Table 4-1.
10.12.2.1 Verify that the design airflow velocity has been balanced by a NEBB Certified TAB Firm prior
to performing the filter installation leak test.
10.12.2.2 Introduce the aerosol into the air supplied to the filters in a manner which will produce a
uniform challenge concentration at each of the filters being exposed at the same time.
10.12.2.3 Measure the upstream particle concentration as the challenge is introduced. Verify that the
upstream particle challenge shall be greater than 3.53 x 107 (35,300,000) particles per cubic meter, (1 x
106 [1,000,000] particles per cubic foot of air). While this concentration will allow a reasonable scan rate,
a higher concentration will improve the accuracy and may allow for increased scan rate.
10.12.2.4 The resulting upstream challenge concentration, along with other information specified below
is used in Equation 10-2 to calculate the Acceptable Scan Rate when utilizing a Discrete Particle
Counter Test.
10.12.2.5 Using the resulting scan rate (Sr), scan the filter face and the perimeter of the filter assembly
by passing the probe in slightly overlapping strokes so that the entire area of the filter and installation is
tested. The probe should be held approximately 25 mm (1 inch) from the area to be tested during
scanning. Separate passes should be made around the entire periphery of the filter, along the bond
between the filter pack and the frame, and around the seal between the filter and the device.
Equation 10-2
Sr =
Where:
=
Sr
=
Cc
Ls
=
=
Fs
Dp
=
Np
=
60
=
Cc Ls Fs D p
60 N p
Acceptable Scan Ratecm/s (in/s)

Upstream challenge concentrationparticles/L (particles/ft3)
Significant leakpercentage of upstream concentration (typically 0.01%)
Sample flow rate of instrument usedL/min (cfm)
Probe dimension parallel to scan directioncm (inches)
Number of particle counts that indicate the leak (1 through 10)
Conversion60 sec/min
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NOTE: If a lower value of Np is used (1), the allowable scan rate will be increased but the probability of
finding a leak will be decreased and the probability of false leaks is increased. If a larger Np is used (3 or
greater) the allowable scan rate is decreased but the probability of detecting a leak is increased.
10.12.2.6 When scanning a filter and the supporting assembly installation a particle count detection
exceeding Np will indicate a potential leak. If particles are registered that exceeds Np, then the particle
concentration penetrating the defect shall be determined if a significant leak exists.
10.12.3 ACCEPTANCE
An unacceptable leak is defined as a sustained reading greater than 0.010% of the measured upstream
concentration for the particle size of interest, or as specified in the contract documents or as agreed to
10.12.4 REPORTING
10.12.5 REPAIRS
10.12.5.1 Filters may be repaired providing:
10.12.5.2 The size of the repair(s) is not greater than 3% of each filter face area. Additionally, a repair
area shall have a minimum dimension which shall not exceed 38 mm (1.5 inches) or as specified in the
10.12.5.3 Repairs to filter installation leaks may be made by procedures specified in the contract
10.13 FILTER INSTALLATION

PENETRATION TEST METHOD
LEAK
TESTS
TOTAL
AEROSOL
The purpose of the total aerosol penetration test method is to verify filter and installation integrity when
downstream access to the filter and installation is not accessible. This method is different than the test
methods identified in Section 10.11 and 10.12 and therefore a significant leak may be in the range of
0.005% up to 0.030% versus a value of 0.010% when using a photometer or a particle counter methods
described above.
This test is performed by introducing challenge aerosol upstream of filters installed in ducts remote to the
cleanroom. The filtered air entering the room from the duct is then measured and compared to the
upstream concentration to determine the overall penetration of the filter installation.
10.13.1.1 An aerosol particle generator as described in Table 4-1.
10.13.1.2 Photometers shall conform to the requirements of Table 4-1.
10.13.2.1 Verify that the design airflow velocity has been balanced by a NEBB Certified TAB Firm
prior to performing the filter installation leak test.
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10.13.2.2 Introduce a minimum of 10 g/L of the aerosol challenge upstream of the filters in a manner
that will produce a uniform challenge to the filter bank. Using a photometer on its 100% scale,
probe the duct and measure the aerosol concentration in the duct directly upstream of the filter(s).
Multiple points should be read across a plane closest to the filter in order to determine whether or not
a uniform concentration is achieved. A minimum of five evenly spaced readings should be taken and
all individual readings should fall within 5% of the average in order to continue. If any individual
reading deviates greater than 5% of the average, then another location must be found for the
introduction of aerosol such that it will meet the uniformity requirements.
10.13.2.3 Locate a place in the ductwork at least ten duct diameters from the filter(s) under test. Using a
photometer set to a scale which will measure 0.030% concentration, probe the duct and measure the
aerosol concentration penetration. Multiple points should be read across a plane in order to determine
whether or not a uniform concentration is achieved. A minimum of five evenly spaced readings should
be taken and all individual readings should fall within 5% of the average in order to continue. If any
individual reading is deviates greater than 5% of the average, then another location must be found for
the downstream reading of aerosol penetration such that it will meet the uniformity requirements.
10.13.3 ACCEPTANCE
10.13.3.1 The downstream measured aerosol concentration should not exceed 0.030% of the upstream
concentration or as specified in the contract documents or as agreed to between the Owner / Buyer and
the NEBB Certified CPT Firm.
10.13.4 REPORTING
See Section 5.11 for the report requirements.
10.13.5 REPAIRS
10.13.5.1 Repairs are not normally made to filters evaluated by the methodology due to inaccessibility.
Most common repair / solution is to replace the filter(s).
10.14 AIRBORNE PARTICLE COUNT CLEANLINESS CLASSIFICATION TEST

ISO STANDARD 14644
The airborne particle count cleanliness classification test is performed to determine the actual particle
count level within the facility at the time of the test (As-Built, At-Rest, or Operational). Particle size(s) of
interest, the room occupancy mode and the room classification shall be known prior to the beginning of
the tests and shall be as specified in the contract documents or as agreed to between the Owner /
Buyer and the NEBB Certified CPT Firm.
A particle counter that meets the requirements of Table 4-1.
10.14.2.1 Verification
Verify that all aspects of the cleanroom system which contribute to its operational integrity (air handling,
filtration systems, walls, ceilings, floors, etc.) are complete and functioning. The following primary tests
shall be completed prior to performing the cleanliness classification tests:
a. Room pressurization tests
b. Airflow tests
c. Filter leak tests
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10.14.2.2 Sample Locations

The minimum number of sample locations is one. If only one sample location is employed then a
minimum of three single sample volumes shall be taken at that single location. Sampling at more
locations than the required minimum will result in greater precision. The minimum number of locations
shall be calculated by taking the square root of the room area in square meters round up to the next
whole number. This is shown in Equation 10-3.
Equation 10-3
SL = RA
Where: SL = Minimum Number of Sample Locations
RA = Room Area in m
10.14.2.3 Sample Location Grid
Establish a test point grid pattern at the work surface elevation uniformly distributed throughout the
cleanroom, except as limited by equipment.
10.14.2.4 Number of Samples
The minimum number of samples shall be 3. The minimum number of samples at any location is one.
More than one sample may be taken at each location.
10.14.2.5 Sample Volume per Location
The single sample volume per location for an ISO classified room shall be per Equation 10-4.
Equation 10-4
Vs =
20
1000
C n ,m
Where:
Vs = Sample Volume (L)
Cn,m
= Class Limit (Number of Particles/m) for the largest considered particle size specified for the
relevant class.
Note: The minimum sample volume shall be 2 liters with a minimum sample time of 1 minute.
10.14.2.6 Particle Size
The size of particles to be measured for room class certification shall be as specified in the contract
documents or as agreed to between the Owner / Buyer and the NEBB Certified CPT Firm. Particle
counts limits for an ISO classified room shall be per Table 10-1 Airborne Particulate Cleanliness
Classes ISO 14644.
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SECTION 10
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TABLE 10-1: Airborne Particulate Cleanliness Classes In Accordance With

ISO Standard 14644
Class limits are given for each class name. The limits designate specific concentrations (particles per
unit volume) of airborne particles with sizes equal to and larger than the particle sizes shown.
Cleanliness Class Limits*
Class
Number
Particle Size per m3
0.1 m
1
2
3
4
5
6
7
8
9
10
100
1,000
10,000
100,000
1,000,000
N/A
N/A
N/A
0.2 m
2
24
237
2,370
23,700
237,000
N/A
N/A
N/A
0.3 m
N/A
10
102
1,020
10,200
102,000
N/A
N/A
N/A
0.5 m
N/A
4
35
352
3,520
35,200
352,000
3,520,000
35,000,000
1.0 m
N/A
N/A
8
83
832
8,320
83,200
832,000
8,320,000
5.0 m
N/A
N/A
N/A
NA
29
293
2,930
29,300
293,000
N/A = Not Applicable

*Concentration limits for other Cleanliness Classes can be calculated from Equation 10-6.
Equation 10-6
Particles/m3 = 10 Cm (0.1 m /Cn)2.08
Where:
Cn = Particle size in microns
Cm = Cleanliness Classification
10.14.3 ACCEPTANCE
The cleanroom or controlled environment shall have met the acceptance criteria for an airborne
particulate cleanliness class (see Table 10-1) when the averages of the particle concentrations
measured at each of the locations fall at or below the class limit. Additionally, if the total number of
locations sampled is greater than one and less than ten, the mean of these averages must fall at or
below the class limit with a 95% UCL. See Appendix C, Section C.5.1.
If the results are non-compliant based on the 95% UCL calculation due to a single outlier value, it does
not need to be included in a recalculation of the 95% UCL analysis provided that the outlier is due to
procedural error or equipment malfunction. Additionally, the calculation is repeated with all remaining
sample locations and at least three samples remain in the calculation. Additionally, the cause of the
outlier is documented. Deletion of the outlier in the 95% UCL calculation shall be as agreed to between
Clean work zones within the cleanroom may also be allowed. These clean work zones shall be
classified based on the maximum allowable particle count within that clean work zone.
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10.14.4 REPORTING
10.15 AIRBORNE PARTICLE COUNTING TESTS SEQUENTIAL SAMPLING

Sequential Sampling Plan For ISO 14644-1
As an alternative method for verifying the compliance of air to the limits of airborne particulate
cleanliness ISO Class 4 and cleaner, the sequential sampling plan described in Appendix F of ISO
14644-1 may be used. The advantage of sequential sampling is the potential to reduce significantly the
sample volume at each location and, consequently, to reduce sampling times.
10.16 ROOM PRESSURIZATION TESTS

The current ISO 14644 Standards do not address cleanroom pressurization, although a pressure
differential of 6 to 25 Pa (0.02 to 0.10 in.w.g.) is generally used, with 12.5 Pa (0.05 in.w.g.) being
common increments between rooms, unless otherwise specified.
An airflow pressure instrument that conforms to the requirements of Table 4-1.
10.16.2.1 Measure and record the pressure differentials in Pa (in.w.g.) between the inner most
cleanroom and adjacent spaces, rooms, or the exterior environment.
10.16.2.2 Measure and record the pressure differential in Pa (in.w.g.) between the next adjacent spaces
and other spaces or the exterior environment until all pressure differentials have been obtained and
recorded.
10.16.3 ACCEPTANCE
Pressurization levels shall be as specified in the contract documents or as agreed to between the
Owner / Buyer and the NEBB Certified CPT Firm.
10.16.4 REPORTING
69
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70
SECTION 11 SECONDARY TESTS

11.1 INTRODUCTION
The secondary tests are user optional and relate to particle and air movement and other ancillary
cleanroom systems:
a.
b.
c.
d.
e.
f.
g.
h.
i.
j.
k.
Airflow Parallelism Tests

Recovery Tests
Lighting Level and Uniformity Tests
Sound Level Tests
Temperature and Humidity Uniformity Tests
Electrostatic Tests
Conductivity Tests
Electromagnetic Interference (EMI) Test
Air Change Rate (ACH) Test
11.2 AIRFLOW PARALLELISM TESTS

The purpose of the airflow parallelism test is to show the actual airflow pattern throughout the unidirectional cleanroom. It can also be used to demonstrate the effects on airflow caused by equipment.
This test should be performed after all airflow velocity and uniformity tests and room pressurization tests
have been performed. Determining the airflow patterns within a room is performed using various
mediums which include the following non contaminating items; vapor source or streamers of thread or
string.
1 1.2.1.1 Test Medium (non-contaminating items; carbon dioxide, glycol or other visible vapor source or
streamers of thread or string).
11.2.1.2 Support stand which will least affect the airflow in the test location aerodynamically, and will
allow the positioning of the test medium at the specified location and height.
11.2.1.3 Plumb bob or spirit level
11.2.1.4 Measuring tape
11.2.1.5 Pointer and stand
11.2.2.1 Divide the cleanroom into grids of equal area having dimensions of 3 m x 3 m (10 feet x 10
feet), or as otherwise specified in the contract documents or as agreed to between the Owner / Buyer
11.2.2.2 Secure plumb line, spirit level, or straight edge as required.
11.2.2.3 Mark the plumb line at 305 mm (12 inch) intervals.
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SECTION 11
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11.2.2.4 The distance from the plumb line to the streamer or vapor is determined at a distance of 915
mm and 1520 mm (36 and 60 inches) above the floor. The length of the plumb line should not exceed
1.2m (4 feet)
11.2.2.5 Introduce the aerosol test medium using the support stand at the specified test grid location
and height.
11.2.2.6 The angle of deflection is then calculated based on the measured horizontal offset from true
vertical. See Appendix C, Section C.8.1
11.2.3 ACCEPTANCE
11.2.3.1 The angle of deflection should not be greater than 14 from center when measured higher than
915 mm (36 inches) above the floor or as otherwise specified in the contract documents or as agreed to
11.2.4 REPORTING
11.3 RECOVERY TESTS

The purpose of the recovery test is to determine the amount of time that is necessary for nonunidirectional cleanrooms or clean spaces and their systems to reach a specified steady state
cleanliness level after a brief particle generation event within the clean space. It is not recommended for
unidirectional airflow clean spaces nor in ISO Class 8 areas. This test must be as specified in the
Note: There is potential for residue from the aerosol to be deposited on the surfaces within the
cleanroom.
11.3.1.1 An aerosol generator that conforms to the requirements of Table 4-2 or airflow visualization
generator
11.3.1.2 A discrete particle counter that conforms to the requirements of Table 4-2.
photometer may be used as an option
An aerosol

11.3.2.1 The number of points and the location of the points is to be determined as specified in the
11.3.2.2 Ensure that the cleanroom HVAC systems are in operation.
11.3.2.3 Set up the particle counter or photometer in accordance with the manufactures instructions.
Note: An aerosol dilutor is recommended when using a particle counter to avoid coincidence loss and
contamination of the optics.
11.3.2.4 The sample probe should not be setup directly under the HEPA filter or room air supply.
Identify poor airflow areas, turbulent zones, etc. within the test area. The sample probe(s) should be
slightly above work surface height or the height of potential product exposure.
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11.3.2.5 Up to four sample locations can be measured using one remote instrument. Sample tubing up
to 8 m (26 feet) in length can run out of the cleanroom to the particle counter / photometer. Samples will
be taken at each location every 15 seconds by sequentially sampling from each tube.
11.3.2.6 Generate a particulate challenge in the cleanroom or clean space to be tested while the air
handling units are in operation. Raise the initial particle concentration 1,000 to 10,000 times the target
cleanliness level.
11.3.2.7 Stop the aerosol challenge, record the start time, and begin aerosol concentration
measurements. Record the aerosol concentration for a 6 second to 12 second sample period for each
minute until the particle count is returned to ten times the target cleanliness level. Record and plot the
particle concentration versus time for each sample location.
11.3.2.8 The recovery time is the time, in minutes, for the particle concentration to decrease two orders
of magnitude, i.e., the time for each location to recover from 1000 times the target concentration to ten
times the target. The slowest recovery location in the cleanroom defines the room recovery rate.
11.3.3 ACCEPTANCE
Acceptable recovery times shall then be determined as specified in the contract documents or as
11.3.4 REPORTING
11.4 LIGHTING LEVEL AND UNIFORMITY TESTS

The purpose of the lighting level and uniformity tests is to verify that installed lighting levels and lighting
uniformity meet the specified requirements. The measurement procedures are adopted from the
Illuminating Engineering Society of North America (IESNA) Lighting HandbookReference Volume.
While the test procedure to be followed will vary based on the exact layout of the luminaries, there are
some common elements that pertain to all of the tests such as: lamp conditioning, measurement
conditions, instrumentation and equipment, creating a representative grid pattern for testing locations,
etc.
11.4.1.1 A portable photoelectric illumination meter shall meet the requirements of Table 4-2.
11.4.1.2 Other equipment needed for the test are:
a. A reflected ceiling plan or a floor plan and if possible a furniture or equipment layout plan
b. A tape measure
c. Brightly colored dots or another means of marking the test locations of the grid
d. A portable test stand that is the height of the work surface, usually 750 mm (30) tall, and
will allow the instrument and the light sensitive cell to be placed horizontally.
11.4.2 TEST PROCEDURES GENERAL (APPLIES TO ALL TESTS)
11.4.2.1 Lamp Conditioning:
a. For high intensity, or fluorescent systems, in relatively new lamp installations, at least 100 hours
of operation should elapse before measurements are taken
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SECTION 11
SECONDARY TESTS
b. With incandescent lamps, seasoning is accomplished in 20 hours or more for common sizes
c. A high intensity discharge or fluorescent system must be illuminated for at least two hours
before measurements are taken to be sure that normal operating output and temperature has been
attained
11.4.2.2 Measurement Conditions:
a. Luminance measurements should be made under actual working conditions. All lighting in the
area including general lighting, task lighting and supplementary lighting should be in normal use
b. Measurements shall be made at work surface elevation and from a specified work point location
with the combinations of daylight and electric lighting facilities available
c. Verify that the thermal conditions of the space are stable
d. Care and consideration should be given to identify the influence of natural lighting sources
11.4.3 TEST PROCEDURE DETERMINATION OF AVERAGE LUMINANCE FROM GENERAL
LIGHTING
11.4.3.1 A measurement grid shall be determined and should be positioned to cover a representative
area of the working plane. Any obstructions above the working plane, away from columns, tall pieces of
equipment, filing cabinets, etc. shall be noted in the report.
11.4.3.2 The use of this method in the types of areas described should result in values of average
luminance within 10 percent of the values that would be obtained by dividing the area into 0.6 m (2
foot) squares, taking a reading in each square and averaging.
11.4.3.3 The measuring instrument should be positioned so that when readings are taken, the surface
of the light sensitive cell is in a horizontal plane and 760 mm (30 inches) above the floor unless
specified in the contract documents or as agreed to between the Owner and the NEBB Certified CPT
Firm.
11.4.4 TEST PROCEDURES SYMMETRICALLY SPACED LUMINARIES IN TWO OR MORE
ROWS (SEE FIGURE 11-1)
11.4.4.1 Take readings at stations r-1, r-2, r-3 and r-4 for a typical inner bay. Repeat at stations r-5, r6, r-7 and r-8 for a typical centrally located bay. Average the 8 readings (R).
11.4.4.2 Take readings at stations q-1, q-2, q-3 and q-4 in two typical half bays on each side of room.
Average the 4 readings (Q).
11.4.4.3 Take readings at stations t-1, t-2, t-3 and t-4 in two typical half bays at each end of room.
Average the 4 readings (T).
11.4.4.4 Take readings at p-1 and p-2 in two typical corner quarter bays. Average the 2 readings (P).
11.4.4.5 Calculate the average level of luminance using Equation 11-1.
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Figure 11-1
Equation 11-1
Average luminance =
Where:
R
Q
T
P
N
M
=
=
=
=
=
=
R(N 1) (M 1) + Q(N 1) + T(M 1) + P

NM
"r" average
"q" average
"t" average
"p" average
Number of luminaries per row
Number of rows
11.4.5 TEST PROCEDURES SYMMETRICALLY LOCATED SINGLE LUMINAIRE (SEE FIGURE

11-2)
11.4.5.1 Take readings at stations p-1, p-2, p-3 and p-4 in all 4 quarter bays.
11.4.5.2 Average the 4 readings (P). This average (P) is the average luminance for the area.
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Figure 11-2
11.4.6 TEST PROCEDURES INDIVIDUAL LUMINARIES IN SINGLE ROW (SEE FIGURE 11-3)
Figure 11-3
11.4.6.1 Take readings at stations q-1 through q-8 in 4 typical half bays located two on each side of
the area. Average the 8 readings (Q).
11.4.6.2 Take readings at stations p-1 and p-2 for two typical corner quarter bays. Average the 2
readings (P).
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Equation 11-2
Average luminance =
Q(N 1) + P
N
Where:
N = Number of luminaries
11.4.7 TEST PROCEDURES TWO OR MORE CONTINUOUS ROWS OF LUMINAIRES (SEE
FIGURE 11-4)
Figure 11-4
11.4.7.1 Take readings at stations r-1 through r-4 located near the center of the area. Average the 4
readings (R).
11.4.7.2 Take readings at stations q-1 and q-2 located at each mid-side of the room and midway of
the room and midway between the outside row of luminaires and the wall. Average the 2 readings (Q).
11.4.7.3 Take readings at stations t-1 through t-4 at each end of the room. Average the 4 readings
(T).
11.4.7.4 Take readings at stations p-1 and p-2 in two typical corners. Average the 2 readings (P).
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Equation 11-3
Average luminance =
Where:
R
Q
T
P
N
M
=
=
=
=
=
=
RN(M 1) + QN + T(M 1) + P
M(N + 1)
"r" average
"q" average
"t" average
"p" average
Number of luminaires per row
Number of rows
11.4.8 TEST PROCEDURES - CONTINUOUS LUMINAIRES IN SINGLE ROW (SEE FIGURE 11-5)
Figure 11-5
11.4.8.1 Take readings at stations q-1 through q-6. Average the 6 readings (Q).
11.4.8.2 Take readings at stations p-1 and p-2 in typical corners. Average the 2 readings (P).
Equation 11-4
Average luminance =
Where:
Q =
P =
N =
QN + P
N +1
"q" average
"p" average
Number of luminaires
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11.4.9 TEST PROCEDURES LUMINOUS OR LOUVER-ALL CEILING (SEE FIGURE 11-6)

11.4.9.1 Take readings at stations r-1 through r-4 located at random in the central portion of the area.
Average the 4 readings (R).
11.4.9.2 Take readings at stations q-1 and q-2 located 2 feet (0.6 meter) from the long walls at
random lengthwise of the room. Average the 2 readings (Q).
11.4.9.3 Take readings at stations t-1 and t-2 located 2 feet (0.6 meter) from the short walls at random
crosswise of the room. Average the 2 readings (T).
11.4.9.4 Take readings at stations p-1 and p-2 located at diagonally opposite corners 2 feet (0.6
meter) from each wall. Average the 2 readings (P).
Figure 11-6
Equation 11-5
Average luminance =
Where:
R
Q
T
P
W
L
=
=
=
=
=
=
R(L 8) (W 8) + 8 Q(L 8) + 8 T(W 8) + 64 P

WL
"r" average
"q" average
"t" average
"p" average
Width of room
Length of room
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11.4.10 TEST PROCEDURES POINT OF WORK MEASUREMENTS

11.4.10.1 With task, general and supplementary lighting in use, the luminance at the point of work
should be measured with the worker in a normal working position.
11.4.10.2 The measuring instrument should be located so that when readings are taken, the surface
of the light sensitive cell is in the plane of the work or of that portion of the work on which the critical
visual task is performedhorizontal, vertical or inclined.
11.4.10.3 Readings may be recorded in a table.
11.4.11 ACCEPTANCE
Acceptable illumination levels shall be as specified in the contract documents or as agreed to between
11.4.12 REPORTING
Report any obstructions above the working plane, away from columns, tall pieces of equipment, filing
cabinets, etc. shall be noted in the report.
11.5 SOUND LEVEL TESTS

The purpose of performing sound pressure measurements will vary based on the occupancy state of the
cleanroom. While the purpose may vary, the procedures are identical. The scope of services for sound
level testing shall be as specified in the contract documents or as agreed to between the Owner / Buyer
and the NEBB Certified CPT Firm. The measurement procedures and reporting requirements are
based on the requirements from the current NEBB Procedural Standards for Measurement of Sound
and Vibration. If sound pressure measurements are required, they shall be performed by a NEBB
Certified S&V Professional.
11.5.1.1 A Sound Level Meter (SLM) meeting the requirements of Table 4-2 shall be utilized to perform all
sound level testing.
11.5.1.2 Provide required filters, wind screen, calibrators, etc. that meet the requirement of Table 4-2.
11.5.2 PRELIMINARY TEST PROCEDURES
11.5.2.1 Contract Document Review and Examination
For sound measurements to be meaningful and the data to be reported accurately, advance
preparations must be completed. The NEBB Certified CPT Professional shall examine the contract
documents, which consist of the contract drawings, the specifications, and the approved submittals, to
become familiar with the project requirements and conditions that may preclude proper sound level
testing of systems and equipment. The contract documents shall be examined for any information
deemed necessary to perform the sound measurements.
The sound criteria established for a project shall be as specified in the contract documents or as agreed
to between the Owner / Buyer and the NEBB Certified CPT Firm. This information may be found in the
Project Specifications, the Contract Drawings or some other part of the Contract Documents. The
Contract Documents shall be examined for the following items:
a. NC, RC, dB(A), and any other sound criteria.
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b. List of any rooms or spaces noted in the specifications that require low noise levels.
c. Schedule of equipment to be isolated.
11.5.2.2 Test Readiness Conditions
a. All construction activities must be completed prior to sound level testing. The cleanroom shall
be in an occupancy state that is as specified in the contract documents or as agreed to
between the Owner / Buyer and the NEBB Certified CPT Firm prior to performing sound level
testing. The sound level testing can be performed in any of the 3 occupancy states (As-Built,
At-Rest, or Operating).
b. From a construction standpoint, verify that the cleanroom envelope is complete.
c. When the sound testing is performed for an As-Built occupancy state, the NEBB Certified CPT
Professional shall verify that all building mechanical/electrical systems have been started, are
operational and completely under functional control. All testing, adjusting and balancing
activities shall be performed prior to sound level testing. The NEBB Certified CPT Professional
shall also verify that all primary cleanroom tests have been completed.
d. When the sound testing is performed for an At-Rest occupancy state, the NEBB Certified CPT
Professional shall verify that all of the requirements of Section 11.5.2.2.c are met. Additionally,
the NEBB Certified CPT Professional shall also verify that the appropriate process equipment
within the cleanroom is operational and completely under functional control and is operating in a
manner that is consistent with the normal intended use of the cleanroom. The process
equipment that should be operating during the sound pressure testing shall be as specified in
the contract documents or as mutually agreed to between the Owner / Buyer and the NEBB
Certified CPT Firm.
e. When the sound testing is performed for an Operational occupancy state, the NEBB Certified
CPT Professional shall verify that all of the requirements of Section 11.5.2.2.d are met.
Additionally, the NEBB Certified CPT Professional shall also verify that all personnel are
stationed at their normal working environment and that process equipment within the cleanroom
is functioning in a manner that is consistent with the everyday active use of the cleanroom. The
process equipment that should be operating during the sound pressure testing shall be as
specified in the contract documents or as mutually agreed to between the Owner / Buyer and
the NEBB Certified CPT Firm.
11.5.3.1 As stated above, the usual purpose of performing sound measurements is to determine the
actual sound level pressures of the cleanroom. In order to accurately determine the sound pressure
levels of the cleanroom, it will be necessary to perform sound measurements when other building
systems/conditions and exterior sound sources are at a minimum level and will not influence
measurements of equipment being tested.
11.5.3.2 Prior to making any sound level measurements a field calibration shall be performed in
accordance with the manufacturers recommendations both before and after sound making level
measurements.
11.5.3.3 Based on the occupancy state, take sound measurements when the appropriate systems,
equipment, personnel, etc. are in place.
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11.5.3.4 Instrument Placement

Position sound level instrument to achieve a direct line-of-sight between the sound source and the
sound-level meter. Unless specified or agreed to between the Owner / Buyer and the NEBB Certified
CPT Firm, take sound measurements at a height approximately 1200 mm (48 inches) above the floor
and at least 900 mm (36 inches) from a wall, column, or any other large surface capable of altering
the measurements.
11.5.3.5 Data measurements
Sound levels measurements are typically reported in terms of dB (Flat or Linear); dB(A), Noise
Criteria (NC) or Room (RC). Sound level measurements of the cleanroom shall be reported in either
Noise Criteria (NC) or Room Criteria (RC). Sound level measurements shall be recorded and
reported in one or both of the following two methods: 1) overall sound levels or 2) in octave bands as
follows:
a. Overall dB (Flat or Linear)
b. The sound level meter shall be set to the Slow time constant
c. In each 1/1(Full) octave band, from 31.5 to 8,000 Hz.
11.5 3.6 Locations
The actual scope of work detailing measurement locations shall be as specified in the contract
documents or as agreed to between the Owner / Buyer and the NEBB Certified CPT Firm. If actual
locations are not identified on the contract documents, a grid shall be prepared so that the minimum
locations meet the following requirements: Minimum of 2 measurements per cleanroom or clean zone
space and at least 1 measurement per 36 m (400 ft).
11.5.4 ACCEPTANCE
Acceptable sound level criteria shall be as specified in the contract documents or as agreed to between
11.5.5 REPORTING
11.6 VIBRATION LEVEL TESTS

The purpose of vibration level testing is to measure the actual vibration levels of the cleanroom and to
report those measurements. The scope of services for vibration measurements shall as specified in the
contract documents or as agreed to between the Owner / Buyer and the NEBB Certified CPT Firm. The
measurement procedures and reporting requirements are based on the requirements from the current
NEBB Procedural Standards for Measurement of Sound and Vibration. If vibration measurements are
required, they shall be performed by a NEBB Certified S&V Professional.
11.6.1.1 A vibration meter (minimum 400 line FFT real time analyzer) that meets the requirements of
Table 4-2.
11.6.1.2 Provide associated required accelerometers, calibrators, etc. that conform to the requirements of
Table 4-2.
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11.6.2 PRELIMINARY TEST PROCEDURES

11.6.2.1 Contract Document Review and Examination
For vibration measurements to be meaningful and the data to be reported accurately, advance
preparations must be completed. The NEBB Certified CPT Professional shall examine the contract
documents, which consist of the contract drawings, the specifications, and the approved submittals, to
become familiar with the project requirements and conditions that may preclude proper vibration
measurement testing of systems and equipment. The contract documents shall be examined for any
information deemed necessary to perform the vibration measurements.
The vibration criteria established for a project shall be as specified in the contract documents or as
agreed to between the Owner / Buyer and the NEBB Certified CPT Firm. This information may be
found in the Project Specifications, the Contract Drawings or some other part of the Contract
Documents. The Contract Documents shall be examined for the following items:
11.6.2.2 Vibration reporting requirements in terms of displacement, velocity and / or acceleration.
a. List of any equipment, rooms or spaces noted in the specifications that require low vibration
levels
b. Schedule of equipment and/ or areas to be vibration isolated
c. Examine submittals for vibration isolators, machinery bases and all other vibration control
equipment to verify whether the equipment furnished to the job is in accordance with the
manufacturer's submittals.
11.6.2.3 Test Readiness Conditions:
a. All construction activities must be completed prior to vibration level testing. The cleanroom shall
be in an occupancy state that is as specified in the contract documents or as agreed to between
the Owner / Buyer and the NEBB Certified CPT Firm prior to performing vibration
measurements. The vibration measurements can be performed in any of the 3 occupancy
states (As-Built, At-Rest, or Operating).
b. From a construction standpoint, verify that the building cleanroom envelope is complete.
c. When the vibration measurements are performed for an As-Built occupancy state, the NEBB
Certified CPT Professional shall verify that all building mechanical/electrical systems have been
started, are operational and completely under functional control. All testing, adjusting and
balancing activities shall be performed prior to vibration measurements testing. The NEBB
Certified CPT Professional shall also verify that all primary cleanroom tests shall be completed.
d. When the vibration measurements are performed for an At-Rest occupancy state, the NEBB
Certified CPT Professional shall verify that all of the requirements of Section 11.6.2.3.c are met.
Additionally, the NEBB Certified CPT Professional shall also verify that the appropriate process
equipment within the cleanroom is operational and completely under functional control and is
operating in a manner that is consistent with the normal intended use of the cleanroom. The
process equipment that should be operating during the vibration level testing shall be as specified
in the contract documents or as mutually agreed to between the Owner / Buyer and the NEBB
Certified CPT Firm.
e. When the vibration measurements are performed for an Operational occupancy state, the NEBB
Certified CPT Professional shall verify that all of the requirement of Section 11.6.2.3.d are met.
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Additionally, the NEBB Certified CPT Professional shall also verify that all personnel are stationed
at their normal working environment and that process equipment within the cleanroom is
functioning in a manner that is consistent with the everyday active use of the cleanroom. The
process equipment that should be operating during the vibration level testing shall be as specified
in the contract documents or as mutually agreed to between the Owner / Buyer and the NEBB
Certified CPT Firm.
11.6.2.4 Test Readiness Report
Prepare a report identifying all issues that would preclude proper vibration measurements of the
cleanroom.
11.6.3.1 As stated above, perform vibration measurements when building systems/conditions and
exterior vibration sources are at normal or maximum level and may influence measurements. In order
to obtain vibration sources, the following should be implemented:
a. Turn on equipment in the building that may be vibration sources
b. Normal human activity should be allowed because it may affect accuracy of vibration
measurements
c. Vibration measurements should be performed when actual cleanroom vibration sources will be
encountered. This may include such items as: exterior vibration sources, trains, roadway
traffic, adjacent construction activities, etc. can be minimized.
11.6.3.2 Based on the occupancy state, take vibration measurements when the appropriate systems,
equipment, personnel, etc. are in place.
11.6.3.3 When attempting to isolate a vibration source, it may be necessary to systematically
shutdown rotating equipment within the cleanroom. In all situations, the NEBB Certified CPT
Professional shall contact the appropriate personnel before shutting down any cleanroom systems or
operating equipment.
11.6.3.4 Location and attachment of accelerometer (transducer):
a. The method of attaching an accelerometer can seriously affect its performance. Accelerometers
should be attached to vibrating surfaces according to the accelerometer manufacturer's
instructions. The accelerometer shall be mounted to surfaces that are flat and clean. If vibration
measurements must be made on vibrating machinery which appears to have exceptionally large
vibration amplitudes, it may be necessary to attach the accelerometer to the machine by means
of threaded metal studs.
b. Heavy accelerometers may affect the accuracy of vibration levels obtained from small or
lightweight systems or equipment.
Accelerometer weight shall be no more than 10% of the
equipment to be tested.
c. It is recommended that the same mounting method be used for all measurements made on any
individual piece of equipment and similar pieces of equipment.
d. The hierarchy of mounting an accelerometer, based on accuracy of repeatable results is: stud
mount, adhesive mount, magnetic base, bees wax, and hand-held probe. The magnetic base
is the most common method of attachment.
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11.6.3.5 Measurement Locations

Measure and record vibration levels at all required equipment bases, equipment and on building
structure adjacent to the equipment. The vibration measurements should be taken in the vertical,
horizontal and axial planes when the measurements can be performed safely. Measure and record
acceleration, velocity, and/or displacement readings. Vibration measurement location shall be based
on the following:
Equipment Bases
Support pedestals and structural components
Location
Within 150 mm (6 in.) of the top of the
support pedestal
Within 150 mm (6 in.) of each isolator or
within 150 mm (6 in.) of the equipment
Vibration sensitive equipment
Equipment and Building Structure

Vibration sensitive equipment
Floor Location
Within 150 mm (6 in.) of equipment
11.6.3.6 Data Measurements

Vibration measurements shall be recorded and reported as follows:
Discrete vibration levels: from 1 to 101 Hz in 0.25 Hz increments.
11.6.3.7 Locations
The actual scope of work shall be as specified in the contract documents or as agreed to between the
Owner/Buyer and the NEBB Certified CPT Firm.
11.6.4 ACCEPTANCE
Acceptable vibration level criteria shall be as specified in the contract documents or as agreed to
11.6.5 REPORTING
11.7 TEMPERATURE AND HUMIDITY UNIFORMITY TESTS

The purpose of the temperature and humidity tests is to document the temperature and humidity levels
in the cleanroom or clean space.
Two levels of temperature and humidity tests are used. The first, general temperature and humidity
uniformity tests, is suited for normal environmental requirements and will be presented in Section 11.8
the second, comprehensive temperature and humidity uniformity tests, will be presented in Section 11.9
and is for areas requiring stricter control.
The general level test is used to demonstrate that the cleanroom HVAC systems will maintain the
specified levels of temperature and humidity required primarily for occupant comfort.
The
comprehensive level test is used to demonstrate that the cleanroom HVAC systems will maintain the
specified levels of temperature and humidity required for both occupant comfort and process
temperature control.
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The scope of services for temperature and moisture uniformity testing shall be as specified in the
11.8 GENERAL TEMPERATURE AND HUMIDITY UNIFORMITY TESTS

11.8.1. INSTRUMENTATION AND EQUIPMENT
11.8.1.1 Temperature measuring devices such as standard thermometers and electronic thermometers
shall conform to the requirements of Table 4-2.
11.8.1.2 Temperature sensing devices such as thermocouples, thermostats, or other temperature
sensors used with readout devices shall conform to the requirements of Table 4-2.
11.8.1.3 Humidity measuring devices including sling psychrometers, electronic thermo-hygrometers and
dew point or humidity sensors shall conform to the requirements of Table 4-2.
11.8.2 TEST PROCEDURES TEMPERATURE
11.8.2.1 Verify completion of HVAC system testing, adjusting and balancing (TAB) work prior to
performing these tests.
11.8.2.2 Allow the HVAC system to operate under automatic control for 24 hours prior to tests.
11.8.2.3 Measure the temperature at a minimum of one location for each temperature control zone.
Place each thermometer or each sensor at the designated location at work level height. Allow time for
the sensor to stabilize sufficiently for accurate readings.
11.8.2.4 Record the time and temperature reading at each location for each temperature control work
zone.
11.8.3 TEST PROCEDURESHUMIDITY
11.8.3.3 The relative humidity is to be measured at a minimum of one location for each humidity
(temperature) control zone. Place the humidity device or sensor at the designated location and height,
allowing the sensor to stabilize.
11.8.3.4 Measure and record the humidity readings simultaneously with temperature readings.
11.8.4 ACCEPTANCE
Acceptable criteria for temperature and humidity levels and requirements shall be as specified in the
11.8.5 REPORTING
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11.9 COMPREHENSIVE TEMPERATURE AND HUMIDITY UNIFORMITY

TESTS
11.9.1.1 Electronic thermometers and temperature sensors that conform to the requirements of Table 42.
11.9.1.2 Humidity measuring instruments and sensors that conform to the requirements of Table 4-2.
11.9.1.3 A data logging device with printable or downloadable data output that conforms to the
requirements of Table 4-2.
11.9.2 PROCEDURES TEMPERATURE AND HUMIDITY
11.9.2.1 Designate a minimum of one temperature and relative humidity measurement location in each
temperature control zone.
11.9.2.2 Multiple locations in each zone may be located as specified.
11.9.2.3 The presence of heat sources should be noted in relation to the test sample location.
11.9.2.5 Verify that the airflow uniformity tests have been completed and accepted.
11.9.2.7 Place each temperature and humidity sensor at each designated work level sampling location
and allow stabilization.
11.9.2.8 Measure and record each temperature and humidity measurement simultaneously at each
location at a minimum of every 6 minutes for a minimum period of 2 hours. It is typical to measure each
area for 22 hours to assure temporal uniformity.
11.9.3 ACCEPTANCE
Acceptable criteria for temperature and humidity levels and requirements shall be as specified in the
11.9.4 REPORTING
11.10 ELECTROSTATIC TESTS

The purpose of the electrostatic test is to benchmark the levels of electrostatic charge, the resistance
properties of surfaces, and the effectiveness of the ionizer charge neutralizing systems.
This test consists of four parts: Measurement of Static Charge Level, Surface Resistance Test,
Ionizer Discharge Time Test and Measurement of Ionizer Offset Voltage.
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While it is possible to measure static charge directly by placing objects in a Faraday Cup, this is often
impractical. The Measurement of Static Charge Level establishes the levels of static charge that are
generated on materials within the test area. It does this by measuring the surface voltage (using an
electrostatic voltmeter for conductors) or charge-generated electric field (using an electrostatic field
meter for insulators or conductors). The Surface Resistance Test determines whether a material may
dissipate a static charge effectively when it is connected to ground. It also determines whether or not
it is connected to ground. By measuring the surface resistance and the resistance to ground on
surfaces, the static-dissipative property can be evaluated.
The Ionizer Discharge Time Test and Measurement of Ionizer Offset Voltage tests relate to the
performance of ionizers used to neutralize charge on surfaces that cannot be grounded or are
insulators. These tests are performed by measuring the discharge time of an initially charged isolated
plate, and by determining the offset voltage (balance) of the ionizer with an initially uncharged isolated
plate. The results of each measurement indicate the efficiency of neutralizing static charges and the
imbalance between the amount of generated positive and negative ions.
The scope of services for these electrostatic tests shall be as specified in the contract documents or as
11.10.1.1 An electrostatic voltmeter or field meter which meets the requirements of Table 4-2.
11.10.1.2 A charged plate monitor (CPM) which meets the requirements of Table 4-2.
11.10.1.3 An ohmmeter and electrodes which meet the requirements of Table 4-2.
11.10.2 TEST PROCEDURES MEASUREMENT OF SURFACE CHARGE LEVEL
11.10.2.1 The measuring point(s) or the object to be measured should be as specified in the contract
documents or as agreed to between the Owner / Buyer and the NEBB Certified CPT Firm. The choice of
test instrument will depend on whether the object(s) to be measured are insulators or conductors and
their physical size. Consult instrument manufacturers instructions for additional information.
11.10.2.2 Hold the instrument probe at the manufacturers specified distance from a grounded metal
plate and adjust the reading of the electrostatic voltmeter or field meter to zero.
11.10.2.3 Hold the probe parallel to the plate and at a distance that is in accordance with the
manufacturers recommendations.
11.10.2.4 The metal plate should have a surface area large enough for the required probe aperture and
be large enough for the probe to surface spacing ratio. Refer to manufacturers instructions
11.10.2.5 According to the manufacturers instructions, place the probe near the surface of an object
which may be charged and measure the surface voltage (of a conductor with an electrostatic voltmeter),
or electric field (of an insulator or conductor with an electrostatic field meter). Record the measurements
at each specified measurement point.
11.10.3 TEST PROCEDURES SURFACE RESISTANCE TESTS
11.10.3.1 Specific test conditions should be as specified in the contract documents or as agreed to
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11.10.3.2 The two electrodes should be set at the correct distance on the surface in accordance with
the manufacturers recommendations. The surface resistance (point to point) can now be measured with
an ohmmeter providing the appropriate output voltage. (Note that standard ohmmeters use too low a
voltage for this purpose. The ohmmeter must have the capability of making measurements at 10 volts
and 100 volts.) Record the measurements at each specified measurement point.
11.10.3.3 One electrode is connected to ground and the other electrode should be placed on the
surface in accordance with the manufacturers recommendations. The surface resistance to ground can
now be measured with an ohmmeter providing the appropriate output voltage. Record the measurements
at each specified measurement point.
11.10.4 TEST PROCEDURES ION GENERATOR TEST
Ionizer performance is evaluated by measuring the discharge time (time to neutralize a known charge)
and the offset voltage. The imbalance of positive and negative ions that are in the ionized airflow are
determined by the offset voltage measurements. The efficiency of eliminating static charges using
ionizers is determined by measuring the discharge time.
11.10.4.2 The instrument specified in industry standards for measuring ionizer performance is known as
a Charged Plate Monitor (CPM). It basically consists of an isolated conductive plate of known
capacitance, a power source for charging the plate to a known voltage or zero, and means to measure
the voltage on the plate and the time it takes to reach a preset level. Consult the manufacturers
instructions for operating procedures.
11.10.4.3 With the CPM placed in the specified measuring point(s), use the power source to charge the
isolated conductive plate to a known positive voltage.
11.10.4.4 As the static charge of the plate is reduced by the ionizer, measure the time for the static
voltage on the plate to be reduced to 10% of the initial voltage condition which is the discharge time.
Record the measurements at each specified measurement point.
11.10.4.5 Repeat this procedure with the plate charged to a known negative voltage. Record the
measurements at each specified measurement point.
11.10.5 TEST PROCEDURES MEASUREMENT OF OFFSET VOLTAGE
11.10.5.2 With the CPM placed in the specified measuring point(s), connect the isolated conductive
plate to ground to remove any residual charge. Adjust the reading of the CPM to zero, if necessary.
Remove the ground connection.
11.10.5.3 Allow sufficient time (typically 1 minute) for the isolated plate to acquire a charge from the
ionizer and the reading to stabilize. Record the reading of the offset voltage. (Note some ionizers
pulse from positive to negative as part of their normal operation. In this case, record the maximum
positive and negative readings of the offset voltage.)
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11.10.6 ACCEPTANCE
Acceptance criteria shall be as specified in the contract documents or as agreed to between the Owner /
Buyer and the NEBB Certified CPT Firm.
Note: The Owner / Buyers criteria will depend on the electrostatic sensitivity of devices that are located
in the work area.
11.10.7 REPORTING
11.11 CONDUCTIVITY TESTS

The purpose of the conductivity test is to measure resistance between specified points on the floor
covering, and from the floor covering to the building ground at strategic locations within the building.
The tests are similar to the requirements of the current edition of NFPA 99, except as modified in the
test procedures. The scope of services for these conductivity tests shall be as specified in the contract
11.11.1.1 An Ohm-meter which meets the requirements of Table 4-2.
11.11.1.2 Two (2) electrodes which meet the requirements of Table 4-2.
11.11.2 TEST PROCEDURES FLOOR TILE TO TILE
Perform conductivity tests between points on the floor covering as follows:
11.11.2.1 Floor shall be tested with temperature and relative humidity maintained as specified in the
11.11.2.2 Measurements, on continuous flooring, shall be made between five pairs of test locations in
each cleanroom or clean space and the results averaged. Measurements shall be made with the
electrodes 0.9 m (3 feet) apart.
11.11.2.3 Measurements on raised floor tiles shall be made between pairs of points and may include
some, or all, of the following:
a.
Diagonal opposite corners of a single tile to test for surface conductivity; i.e .floor waxes that
are insulting (non-conductive)
b.
Corner of test tile to corner of any tile two positions away
Center of test tile to any supporting pedestal
d.
Center of test tile to conductive paint finish covering main structural concrete floor
11.11.3 TEST PROCEDURES FLOOR TO BUILDING GROUND

Perform conductivity tests from the floor covering to the building ground (raised floors only).
11.11.3.1 Floor shall be tested with temperature and relative humidity maintained as specified in the
90
SECTION 11
SECONDARY TESTS
11.11.3.2 Measurements shall be made at 20 tests locations as specified in the contract documents
or as agreed to between the Owner / Buyer and the NEBB Certified CPT Firm. Measurements may be
made between up to five pairs of test locations at each of the 20 test locations in each room and the
results averaged.
11.11.3.3 Measurements shall be made with the one electrode on the floor connected to the
ohmmeter. The other terminal of the ohmmeter shall be connected to the nearest building column or
exposed grounding conductor.
11.11.4 ACCEPTANCE
11.11.4.1 Acceptance criteria shall be as specified in the contract documents or as agreed to between
Note: Typically, the floor panel-to-panel tests achieve average values less than 1 mega ohm and the
floor-to-building ground tests achieve average values less than 1 mega ohm.
11.11.5 REPORTING
11.12 ELECTROMAGNETIC INTERFERENCE (EMI) TEST

The purpose of the Electromagnetic Interference (EMI) Test is to determine the amount of
electromagnetic radiation that is being emitted by electrical circuits. The magnetic fields around the
electrical source can effect sensitive equipment, especially those that use electron beams. Examples
are electron microscopes and e beam lithography equipment. The electron beams are controlled and
focused with magnets. Unwanted and uncontrolled magnetic fields in close proximity to the
equipment results in reduced performance of the instrumentation.
11.12.1.1 A magnetic field meter that meets the requirements of Table 4-2.
11.12.1.2 A magnetic field sensor that meets the requirements of Table 4-2
11.12.2.1 Determine the expected cleanroom position of the electron beam in the equipment to be
installed. Conduct an extensive survey along the position of the future e beam by measuring three
axis (x, y, and z) in at least four locations. Additional locations may be measured 0.5 meters around
the expected path of the e beam when is installed. Test other locations as specified in the contract
11.12.2.2 The source of any readings exceeding 1.0 milligauss shall be determined.
11.12.3 ACCEPTANCE
Acceptance criteria shall be as specified in the contract documents or as agreed to between the Owner
/ Buyer and the NEBB Certified CPT Firm.
11.12.4 REPORTING
See section 5.24 for reporting requirements.
91
SECTION 11
SECONDARY TESTS
11.13 AIR CHANGE RATE (ACH) TEST

The purpose of the air change rate test is to determine the number of times the air is being exchanged
within the cleanroom on an hourly basis. The Air Change Rate per Hour (ACH) is determined by
measuring the total amount of airflow being supplied or returned from the cleanroom and by
calculating the overall volume of the cleanroom.
11.13.1.1 A direct reading flowhood meeting the requirements of Table 4-2
or
11.13.1.2 A manometer and a Pitot tube meeting the requirements of Table 4-2
11.13.2 TEST PROCEDURE
11.13.2.1 Determine if the cleanroom is under a positive or negative pressure.
11.13.2.2 If the pressure is positive, measure and record the supply airflow volume delivered through
the filter using a flow hood. Use appropriate size capture enclosure for each filter application when
using an airflow volume direct reading flowhood.
11.13.2.3 If the pressure is negative, measure and record the return / exhaust airflow volumes being
captured by all return openings and process exhaust devices using the appropriate instrumentation for
the application.
11.13.2.4 Measure the volume of the cleanroom space.
11.13.2.5 Calculate the Air Change Rate per Hour. See Appendix C, Section C.10.
11.13.3 ACCEPTANCE CRITERIA
11.13.4 REPORTING
11.14 BENCH SCAN FILTER LEAK TESTS

The purpose of this test is to determine the integrity of each filter shipment by spot testing random statistical
samples prior to filter installation.
11.14.1.1 An aerosol photometer, aerosol generator and scanning probe that meet the requirements
of Table 4-2.
or
11.14.1.2 A particle counter, microsphere generator and scanning probe that meet the requirements
of the requirements of Table 4-2.
11.14.1.3 A test bench with a fan capable of delivering the specified airflow volume of the installed
filter(s). The fan shall be capable of supplying the air in a uniform manner upstream of the face of
filter(s). The bench filter seal must prevent excessive aerosol from escaping into the environment
92
SECTION 11
SECONDARY TESTS
around the filter(s) under test.

11.14.2 TEST PROCEDURE
11.14.2.1 Test every filter, or if owner approved, develop a statistical sample based on the following:
a. Test all filters which show signs of damage
b. Test every fifth filter and upon failure, test additional untested filters as agreed to between the NEBB
Certified CPT Firm and the Owner
11.14.2.2 Provide flow test bench, aerosol photometer and oil generator (either Laskin nozzle or thermal) or
optical laser particle counter, and microsphere generator and a particle controlled environment.
11.14.2.3 Introduce aerosol oil challenge or microsphere challenge upstream of the filter. A minimum
challenge shall be 10g/l of oil or at least 210,000,000 particles per cubic meter (6,000,000 particles per
cubic foot).
11.14.2.4 Measure the upstream challenge of each filter.
11.14.2.5 Scan the entire downstream filter face area in overlapping strokes, moving at the calculated scan rate
spaced a distance of 25 mm (1 inch) from the filter face.
11.14.2.6 Repairs, leaks and retesting of filters shall be performed in accordance with the requirements
as stated in the contract documents or as agreed to between the Owner/Buyer and the NEBB CPT
Firm.
11.14.3 ACCEPTANCE CRITERIA
11.14.4 REPORTING
93
SECTION 11
SECONDARY TESTS
94
APPENDIX A SAMPLE
CLEANROOM SPECIFICATIONS
The NEBB CPT Committee has developed Cleanroom Performance Testing specifications that can be
utilized by a design professional and incorporated into their contract documents. They are available
for download on the NEBB website at: www.nebb.org.
There are two distinct complete specifications that have been developed:
APPENDIX A-1
Appendix A-1 Sample Specification is for the Microelectronics and Semiconductor industry
requirements.
APPENDIX A-2
Appendix A-2 Sample Specification is for the Bio-Medical and / Pharmaceutical industry
requirements.
Both specifications are identical for Part 1 General and for Part 2 Products. Part 3 Execution
has been tailored for each of the industry requirements.
Either of the specifications is available in electronic format (MS Word) for the design professional to
edit for each projects specific requirements.
As with any sample or master format specification, it is the responsibility of the design engineer of
record to edit the specification for each projects unique specific requirements. These requirements
should include, but are not limited to the following:
a. Specifying the tests to be performed, the parameters to be measured and the acceptable
tolerances. NEBB standards and procedures define industry best practices to perform the
testing.
b. Defining who retains the services of the NEBB Certified CPT Firm and require that the NEBB
Certified CPT Firm be retained early in the construction process.
c. Defining the applicable standards, cleanliness classification(s), acceptance criteria, etc. prior
to submission of project fees; i.e. ISO Class 4 at 0.3 microns (m).
d. Clearly identifying on the architectural, mechanical and electrical plans and in the
specifications, the system components required for cleanroom testing; i.e. pressure
relationships, cleanroom reflected ceiling plans, cleanroom floor plans, etc.
e. Specifying that the building and/or HVAC control system be commissioned and documented
per NEBB Commissioning Standards and Procedures before the cleanroom testing work
begins.

f.
APPENDIX A
Specifying that the air and water systems be Tested, Adjusted and Balanced (TAB) and
documented per NEBB Procedural Standards for Testing, Adjusting, Balancing of
Environmental Systems before the cleanroom testing work begins.
g. Specifying that the building control system firm provides access to hardware and software, or
CPT Firm.
h. Providing adequate access to all equipment and components required by the cleanroom
testing process.
i.
Completely defining validation / commissioning support responsibilities for the NEBB Certified
CPT Firm.
j.
Identifying all project specific requirements that relate to unique safety, reporting, facility
access, etc. which may affect the cleanroom performance testing.
See Section 3 for additional content.
II
APPENDIX A-1 SAMPLE

MICROELECTRONICS & SEMICONDUCTORS
The suggested specification is available on the NEBB website at: www.nebb.org
III
APPENDIX A-1
SAMPLE CLEANROOM SPECIFICATION
MICROELECTRONICS & SEMICONDUCTORS
IV
APPENDIX A-2 SAMPLE

BIO-MEDICAL & PHARMACEUTICAL
The suggested specification is available on the NEBB website at: www.nebb.org
APPENDIX A-2
SAMPLE CLEANROON SPECIFICATION
BIOMEDICAL & PHARMACEUTICAL
VI
APPENDIX B REFERENCES
AND REFERENCED
PUBLICATIONS
American Conference of Governmental Industrial Hygienists (ACGIH)

Kemper Meadow Drive, Cincinnati, Ohio 45240
ACGIH Industrial Ventilation, A Manual of Recommended Practice
Contains information on the design and installation of industrial ventilation systems
and exhaust systems and hoods.
American Glovebox Society (AGS)
P.O. Box 9099, Santa Rosa, California 95405
AGS GUIDELINES FOR GLOVEBOXES
This document provides information for designers, fabricators, and users regarding the
proper, safe, and consistent design, fabrication, and operation of gloveboxes, while
minimizing the cost involved. It guides the designer away from common ergonomic
mistakes made when designing gloveboxes and provides information on installation,
maintenance, decontamination, and decommissioning considerations. The document
establishes standard features for design and fabrication of gloveboxes such that, when
followed, minimize fabrication costs and improve operability. Other important issues
relevant to gloveboxes that are addressed in the Guideline include quality assurance,
glovebox-interior protective linings and coatings, safety, considerations for interior
equipment, and radiological shielding.
AGS STANDARDS OF PRACTICE (SOPs)
The AGS has also published several Standards of Practice (SOPs). Three that are
currently available for purchase are The Standard of Practice for the Design and
Fabrication of Glovebags, AGS-G002, The Standard of Practice for the Application of
Linings to Gloveboxes, AGS-G003, The Standard of Practice for the Specifications of
Gloves for Gloveboxes AGS-G005 and The Standards of Practice for the Design &
Fabrication of Nuclear Application Gloveboxes AGS-G006.
American Society of Heating, Air Conditioning and Refrigerating Engineers (ASHRAE)
1791 Tullie Circle Northeast, Atlanta, Georgia 30329
ASHRAE HandbookHVAC Applications
Chapter on Health Care Facilities
Chapter on Laboratory Systems
Chapter on Clean Spaces
ASHRAE Standard 52.2 Method of Testing General Ventilation Air-Cleaning Devices
for Removal Efficiency by Particle Size.
This standard defines unified test procedures and apparatus for evaluating filters with
efficiencies below that of HEPA filters.
VII
APPENDIX B
REFERENCES & REFERENCED PUBLICATIONS
American Society for Testing and Materials (ASTM)

100 Barr Harbor Drive, West Conshohoken, Pennsylvania 19428
ASTMF 50 Practice for Continuous Counting and Sizing of Airborne Particles in DustControlled Areas and Clean Rooms Using Instruments Capable of Detecting Single SubMicrometer and Larger Particles
Particle concentration and size distribution of airborne particles are determined in
cleanrooms for particles of approximately 0.01 m to 5 m in concentrations up to 3.5 x
106 per cubic meter. Sample acquisition and instrument performance requirements are
stated.
ASTMF 328 Practice for Determining Counting and Sizing Accuracy of an Airborne
Particle Counter Using Near-Monodisperse Spherical Particles.
Size and counting accuracy determination procedures are given for verifying operation of
an optical airborne particle counter.
Monosized latex particles are used for size
definition and counting data are obtained in comparison with a referee method to define
counting accuracy.
ASTMF 649 Practice for Secondary Calibration of Airborne Particle Counter using
Comparison Procedures
Procedures are given for fine-tuning response of an airborne particle counter to match
that of a standard counter for defining atmospheric dust, following calibration with monodisperse latex particles. The procedures are helpful in correlating different counters.
ASTM-F 1471 Air Cleaning Performance of High-Efficiency Particulate Air Filter Systems
Institute of Environmental Sciences and Technologies (IEST)
Arlington Place One, 2340 South Arlington Heights Road, Suite 100, Arlington Heights, Illinois 60005
IEST-RP-CC001 HEPA and ULPA Filters
This recommended practice covers basic provisions for HEPA and ULPA filter units.
Filter performance, materials, design, construction, and testing are covered. Six levels of
performance and six grades of construction are included.
IEST-RP-CC006 Testing Cleanrooms
This recommended practice covers testing methods for characterizing performance of
cleanrooms. Airflow, filter integrity, particle levels, air pressure, air flow parallelism, room
integrity, particle fallout, temperature and relative humidity, light, noise, and vibration are
tested.
IEST-RP-CC013 Equipment Calibration of Validation Procedures
This recommended practice defines applicable test procedures for calibrating
instruments used in cleanrooms and clean air devices, and defines calibration intervals.
IEST-RP-CC014 Calibration of Particle Counters
This recommended practice establishes definitions and procedures for calibrating
counting devices used in cleanroom and establishes some instrument specifications.
IEST-RP-CC018 Cleanroom HousekeepingOperating and Monitoring Procedures
This recommended practice provides guidance for maintaining a cleanroom at the level
for which it was designed. It is a guide for establishing appropriate housekeeping
VIII
APPENDIX B
procedures, along with provision of test procedures to verify effectiveness of the

housekeeping operations.
IEST-RP-CC022 Electrostatic Charge in Cleanrooms and Other Controlled Environments
This practice discusses methods for specifying and evaluating effectiveness of
techniques for controlling electrostatic charge. Test methods are given, along with
guidelines for verifying charge neutralization and resistivity of materials.
IEST-RP-CC023 Microorganisms in Cleanrooms
This recommended practice provides guidelines for the control and measurement of
viable contamination in the air and on surfaces in cleanrooms. Some of the disinfectants
now available are also described.
IEST-RP-CC026 Cleanroom Operations
This recommended practice provides guidance for maintaining integrity of the cleanroom
during ancillary operation, as material preparations, facility modifications, equipment
repair, etc. Procedures are given for verifying cleanliness of equipment and work areas.
IEST-RP-CC034 HEPA and ULPA Filter Leak Tests
This recommended practice covers definitions, equipment, and procedures for leak
testing HEPA and ULPA filters at the factory, the site of installation and after installation.
ISO 14644-1 Classification of Air Cleanliness
This is the first in a series of standards developed by the International Standards
Organization (ISO) addressing contamination control. This standard addresses the
requirements for the different cleanliness classifications. Cleanrooms and associated
controlled environments provide for the control of airborne particulate contamination to
levels appropriate for accomplishing contamination-sensitive activities. Products and
processes that benefit from the control of airborne contamination include aerospace,
microelectronics, pharmaceuticals, medical devices, healthcare, food, and others.
Many factors besides airborne particulate cleanliness must be considered in the
design, specification, operation, and control of cleanrooms and other controlled
environments. These are covered in some detail in other parts of the ISO 14644.
ISO 14644-2 Specifications for Testing and Monitoring to Prove Continued Compliance
with ISO 14644-1
This document provides a mechanism to prove continued compliance with ISO 146441 and specifies minimum requirements for testing and monitoring. In any testing plan,
consideration should also be given to the particular operational requirements, risk
assessment of the installation and its use.
ISO 14644-3 Test Methods
This part of ISO 14644 specifies test methods for designated classification of airborne
particulate cleanliness and for characterizing the performance of cleanrooms and clean
zones. Performance tests are specified for two types of cleanrooms and clean zones:
those with unidirectional flow and those with non-unidirectional flow, in three possible
occupancy states: as-built, at-rest and operational. The test methods recommend test
apparatus and test procedures for determining performance parameters. Where the
test method is affected by the type of cleanroom or clean zone, alternative procedures
are suggested. For some of the tests, several different methods and apparatus are
recommended to accommodate different end-use considerations.
IX
APPENDIX B
ISO 14644-4 Design, Construction and Start-up

This document specifies the requirements for the design and construction of the
cleanroom facilities but does not prescribe specific technological nor contractual means
to meet the requirements. It is intended for use by purchasers, suppliers, and
designers of cleanroom installations and provides a check list of important parameters
of performance. Construction guidance is provided, including requirements for start up
and qualification. Basic elements of design and construction needed to ensure
continued satisfactory operations are identified through the consideration of relevant
aspects of operation and maintenance.
ISO 14644-5 Operation
This document provides those basic requirements for operating and maintaining
cleanrooms and associated controlled environments to meet the standards of the
particular cleanroom as designed, built, and used. This standard addresses
requirements that are basic to the operation of all cleanrooms regardless of the
application.
ISO 14644-6 Vocabulary
This document harmonizes the definitions of terms used in describing materials and
processes relating to cleanrooms and associated controlled environments.
ISO 14644-7 Separative Devices(Clean Air Hoods, Gloveboxes, Isolators, and
Minienvironments)
This section defines the performance requirements in areas of minienvironments and
isolators. These requirements will focus on ways that minienvironments differ from
cleanrooms in the area of monitoring, design, testing, molecular contamination,
material compatibility, integrity, and microbial contamination.
ISO 14644-8 Classification of Airborne Molecular Contamination
This part of ISO 14644 covers the classification of airborne molecular contamination
(AMC) in cleanrooms and associated controlled environments, in terms of airborne
concentrations of specific chemical substances (individual, group or category) and
provides a protocol to include test methods, analysis and time weighted factors within
the specification for classification.
National Environmental Balancing Bureau (NEBB)
8575 Grovemont Circle, Gaithersburg, Maryland 20877
Procedural Standards for Certified Testing of Cleanrooms
This manual provides an extensive array of information on cleanroom testing, technology
and test procedures. It includes: standards issues dealing with the NEBB Cleanroom
program, requirements of the Certified CPT Firm, Certified CPT Professionals,
instrumentation requirements, reporting requirements, standard operating procedures
and exacting procedural issues for all primary and secondary cleanroom tests. Also
included is a sample specification, listing of cleanroom references, and engineering and
statistical data and examples.
Study Course for Certified Testing of Cleanrooms
This is a self-study course in cleanrooms, cleanroom design and systems including
cleanroom testing equipment, control systems, cleanroom test procedures and
cleanroom equipment and accessories. The package includes multiple lessons plus a
X
APPENDIX B
study course examination, reference material and associated engineering and statistical
materials.
Procedural Standards for Fume Hood Performance Testing
This manual provides a basis for the fume hood testing program by providing Certified
Firm and Certified Professional requirements, instrumentation and reporting
requirements and step-by-step testing procedures in evaluating fume hood performance.
It also includes a sample specification, references, and sample reporting forms.
Procedural Standards for the Measurement of Sound and Vibration
This publication provides step-by-step comprehensive guidance for obtaining and
recording sound and vibration data on HVAC systems. Topics include: instrumentation,
inspection of building construction and conditions, interior and exterior sound
measurement, and vibration measurement procedures. Also covered are sample
specifications and sample reporting forms.
Sound and Vibration Design and Analysis
A concise coverage of sound and vibration as it relates to HVAC systems. Basic
concepts of the science of sound and vibration are covered, plus the most current
information on equipment sound levels, duct element regenerated and sound power and
attenuation, duct breakout and break-in, sound transmission in indoor and outdoor
spaces, and vibration analysis. It includes references and glossary.
Study Course for Measuring Sound and Vibration
A home study course on measuring sound and vibration, it guides the student in an
orderly sequence, with diagrams, charts and problems to recognize principles and
procedures. The package includes multiple lessons and final examination, associated
reference texts and binder.
Environmental Systems Technology
A full length, hard-back "collectors type" textbook in a distinctive Victorian style
incorporating HVAC system history and fundamentals, engineering principles, system
design, equipment components and installation, testing and balancing, controls,
acoustics, and an extensive glossary and set of engineering tables.
Procedural Standards for Testing, Adjusting, Balancing of Environmental Systems
A "how-to" set of procedural standards that provide systematic methods for testing,
adjusting, and balancing (TAB) of HVAC systems includes sections on TAB instruments
and calibration, report forms, and sample specification.
Testing, Adjusting, Balancing Manual for Technicians
A practical field-use manual for balancing technicians designed to be used for reference
and job site application as well as for training balancing crews. This edition includes a
section on mathematics and equations for field use.
Procedural Standards for Building Systems Commissioning
This manual serves a comprehensive guide for commissioning building systems. The
text describes the commissioning process, organization, planning, procedures and
methods for verifying and documenting the performance of building systems. There are
focus section on the commissioning of HVAC, Plumbing and Fire Protection Systems.
XI
APPENDIX B
National Fire Prevention Association (NFPA)

1 Batterymarch Park Quincy, Massachusetts
NFPA 318 Standard for the Protection of Semiconductor Fabrication Facilities
The document provides requirements for fire protection systems utilized in
semiconductor fabrication facilities.
NSF International (National Sanitation Foundation) (NSF)
789 N. Dixboro Road, Ann Arbor, Michigan 48113
NSF 49 Class II (Laminar Flow) Biosafety Cabinetry
This document applies to cabinetry designed to minimize hazards inherent in work with
low and moderate risk biological agents and defines tests which must be passed.
United States of America, Agencies & Departments
Air Force Headquarters, AFCL/DAPD
Wright-Patterson AFB, Ohio 45433
H.1 AFM 88-4 Chapter 5 Criteria for Air Force Clean Facility Designs and Construction
Prescribed criteria for the design and construction of Air Force clean facilities. It specifies
the real property standards for meeting the requirements of Air Force TO 00-25-203.
H.2 TO 00-25-203 Contamination Control of Aerospace Facilities, U.S. Air Force
This document specifies cleanroom design, operating, and test procedures. It also
includes recommended cleanliness levels for typical operations.
Food and Drug Administration
5600 Fishers Lane, Rockville, Maryland 20857
Current Good Manufacturing Practice 21CFR 211(cGMP)
Required facility status, manufacturing procedures, personnel action, facility and product
cleanliness as well as required record formats are summarized. This document is vital
for all pharmaceutical manufacturing.
Guidelines to Inspections of Aseptic Processing and Packaging for the Food Industry
This document is reference materials for investigators and other FDA personnel and
provides aseptic processing guidelines.
NASA
John F. Kennedy Space Center, Orlando, Florida 32815
MSFC-STD-246A Standard for Design and Operation Criteria of Controlled
Environmental Areas
Design criteria and operating guide lines are given for clean areas at MSFC facilities.
Standardization Documents Order Desk
Building 4D, 700 Robbins Avenue, Philadelphia, Pennsylvania 1911-5094
MIL-STD-1246C Product Cleanliness Levels and Contamination Control Program
This document provides a basis and a uniform method to specify cleanliness levels and
contamination control program requirements. Cleanliness classification levels are given.
National Technical Information Service
U.S. Department of Commerce, 5285 Port Royal Road, Springfield, Virginia 22161
NTIS/NASA SP-5045 Contamination Control Principles
Document provides a broad overview and guidelines to those designing or planning
cleanroom facilities.
XII
APPENDIX B
NTIS/NASA SP-5074 Cleanroom Technology

Document provides considerable information on history, need, nature and type of
cleanrooms with details of cleanroom environment and operation.
NTIS/NASA SP-5076 Contamination Control Handbook
Extensive detail on contaminants and their control and cleaning methods.
The Naval Publications and Forms Center
5801 Tabor Avenue, Philadelphia, Pennsylvania 19120
NPFC/MIL-HDBK-406 Contamination Control TechnologyCleaning Materials for
Precision Precleaning and Use in Clean Rooms and Clean Work Stations
Document contains extensive information on selection and use of cleaning materials
developed by DOD.
NPFC/MIL-HDBK-407
Contamination Control TechnologyPrecision Cleaning
Methods and Procedures
Document contains extensive information on cleaning methods used by the military
services for gross and precision cleaning of work processed under controlled
environment conditions.
NPFC/MIL-F-0051068 Military Specification: Filter, Particulate, High-Efficiency, Fire
Resistant
Document covers design, construction, and performance of HEPA filters in six sizes and
seven types.
NPFC/MIL-F-51079 Military Specification: Filter Medium, Fire-Resistant, High-Efficiency
Provides requirements and test methods for determining compliance for one grade of
HEPA filter medium.
NPFC/MIL-F-51477 Military Specification: Filters, Particulate, High-Efficiency, Fire
Resistant, Biological Use
Covers general requirements for particulate filters for use in air cleaning or air filtration
systems involving chemical, carcinogenic, radiogenic, or hazardous biological particles.
Federal Std. 209E Airborne Particulate Cleanliness Classes in Cleanrooms and Clean
Zones
This document establishes standard cleanliness classes for cleanrooms and clean
zones, based on specified concentrations of inert airborne particles. It prescribes
methods for verifying air cleanliness using statistical methodology.
USP Publication 797 Pharmaceutical Compounding Sterile Preparations
This document provides sample documents describing high-level pharmacy
requirements for compliance with the regulation
British Standard (BS EN 1822)
789 N. Dixboro Road, Ann Arbor, Michigan 48113
NSF 49 Class II (Laminar Flow) Biosafety Cabinetry
This document applies to cabinetry designed to minimize hazards inherent in work with
low and moderate risk biological agents and defines tests which must be passed.
XIII
APPENDIX B
European Commission (EU)

B1029 Brussels, Belgium, Europe phone (32-2) 299 11 11
EU Guidelines to Good Manufacturing Practice of Medicinal Products for Human and
Veterinary Use.
Annex 1 Manufacture of Sterile Medicinal Products
This document provides guidance for particle limits in cleanrooms within the European
community.
XIV
APPENDIX C ENGINEERING
FORMULAS, EQUIVALENTS &
EXAMPLES
C.1 HVAC ENGINEERING FORMULA (SI UNITS)
C.1.1 AIR EQUATIONS
A.
V = 1.414 (VP/d)
where
V=
Velocity
d=
density, d = 3.48 (Pb/T)
B.
V = (1.66 VP) for Std. air (d = 1.204 kg/m3)
C.
TP = VP + SP
D.
V = VM (d / 1.204)
E.
Airflow Volume (L/s) = 1000 Area Volume
C.2 HVAC ENGINEERING FORMULA (IP UNITS)

C.2.1 AIR EQUATIONS
A.
V = 1096 (VP/d)
where
V=
Velocity
d=
density, d = 1.325 (Pb/T)
B.
V = 4005 (VP) for Std. air (d = .075 lbs/ft3)
C.
TP = VP + SP
D.
V = VM (d / 0.075)
E.
Airflow Volume (cfm) = Area Volume
XV
APPENDIX C
ENGINEERING FORMULAS,
EQUIVALENTS & EXAMPLES
C.3 METRIC EQUIVALENTS

QUANTITY
acceleration
airflow
volumetric flow
rate
area
atmospheric
pressure
distance,
length, or
displacement
lighting
intensity
lighting power
pressure
temperature
velocity
volume
SYMBOL
m/s
m/s
L/s
m/hr
m
mm
kPa
Bar
M
M
mm
Lx
lm/m
Lm
kPa
Pa
C
m/s
m
UNIT
meters per second squared
cubic meters per second
liters per second
cubic meters per hour
square meter
square millimeters
kiloPascals
Barometers
meter
meter
millimeter
Lux
Lumens/square meter
Lumen
kiloPascals =1000 Pascals
Pascals
degrees Celsius
meters per second
cubic meters
XVI
IP RELATIONSHIP
1 m/s = 3.281 ft/sec
1 m/s = 2118.88 cfm
1 L/s = 2.12 cfm
1 m/hr = 0.589 cfm
1 m = 10.76 ft
1 mm = 0.0016 in
101.325 kPa = 29.92 in. Hg = 14.696 psi
1 Bar = 29.92 in. Hg = 14.696 psi
1 m = 3.281 ft.
1 m = 39.37 inches
1 mm = 0.039 inches, 1 inch = 25.4 mm
1 lx = 0.0929 fc
1 lm/m = 0.0931 fc
1 Lm = 0.001496 watts
1 kPa = 0.296 in. Hg = 0.145 psi
1 Pa = 0.004015 in.w.g.
C = (F 32)/1.8
1 m/s = 196.9 fpm
1 m = 35.31 ft
XVII
0.87
0.79
0.73
0.69
0.65
0.60
0.55
0.51
0.48
0.45
0.42
0.40
0.38
0.36
0.34
0.32
0.29
0.90
0.82
0.76
0.71
0.68
0.62
0.57
0.54
0.50
.047
0.44
0.42
0.39
0.38
0.35
0.33
0.30
0.93
0.85
0.79
0.74
0.70
0.65
.060
0.56
0.52
0.49
0.46
0.43
0.41
0.39
0.37
0.34
0.31
0.97
0.89
0.82
.077
0.73
0.67
0.62
0.58
0.54
0.51
0.48
0.45
0.43
0.41
0.39
0.35
0.32
1.01
0.91
0.85
0.80
0.75
0.69
0.64
0.60
0.56
0.52
0.49
0.46
0.44
0.42
0.40
0.37
0.33
1.05
0.95
0.88
0.83
0.78
0.72
0.66
0.62
0.58
0.54
0.51
0.48
0.45
0.44
0.41
0.38
0.35
1.09
0.99
0.92
0.86
0.81
0.75
0.69
0.64
0.60
0.56
0.53
0.50
0.47
0.45
0.43
0.39
0.36
1.13
1.03
0.95
0.89
0.85
0.78
0.71
0.67
0.62
0.58
0.55
0.52
0.49
0.47
0.45
0.41
0.37
1.17
1.07
0.99
0.93
0.88
0.81
0.74
0.70
0.65
0.60
0.57
0.54
0.51
0.49
0.46
0.43
0.39
1.22
1.11
1.02
0.96
0.92
0.84
0.77
0.72
0.67
0.62
0.60
0.56
0.53
0.51
0.48
0.44
0.40
1.08
1.00
0.91
0.85
0.79
0.74
0.70
0.66
0.62
0.59
0.56
0.54
0.51
0.49
0.47
0.46
0.44
Air Temp C
0
20
50
75
100
125
150
175
200
225
250
275
300
325
350
375
400
71.9
3000
76.0
2500
80.0
2000
83.1
1750
85.1
1500
88.2
1250
90.2
1000
93.2
750
96.3
500
98.3
250
101.3
Sea
Level
Barometer (kPa)
Altitude (m)
Table C-1: Air Density Correction Factors (SI Units) Standard Air Density (Sea Level and 20C) = 1.204 kg/m3 at 101.325 kPa
C.4 AIR DENSITY CORRECTION FACTORS
XVIII
0.87
0.79
0.73
0.69
0.65
0.60
0.55
0.51
0.48
0.45
0.42
0.40
0.38
0.36
0.34
0.32
0.29
0.90
0.82
0.76
0.71
0.68
0.62
0.57
0.54
0.50
.047
0.44
0.42
0.39
0.38
0.35
0.33
0.30
0.93
0.85
0.79
0.74
0.70
0.65
.060
0.56
0.52
0.49
0.46
0.43
0.41
0.39
0.37
0.34
0.31
0.97
0.89
0.82
.077
0.73
0.67
0.62
0.58
0.54
0.51
0.48
0.45
0.43
0.41
0.39
0.35
0.32
1.01
0.91
0.85
0.80
0.75
0.69
0.64
0.60
0.56
0.52
0.49
0.46
0.44
0.42
0.40
0.37
0.33
1.05
0.95
0.88
0.83
0.78
0.72
0.66
0.62
0.58
0.54
0.51
0.48
0.45
0.44
0.41
0.38
0.35
1.09
0.99
0.92
0.86
0.81
0.75
0.69
0.64
0.60
0.56
0.53
0.50
0.47
0.45
0.43
0.39
0.36
1.13
1.03
0.95
0.89
0.85
0.78
0.71
0.67
0.62
0.58
0.55
0.52
0.49
0.47
0.45
0.41
0.37
1.17
1.07
0.99
0.93
0.88
0.81
0.74
0.70
0.65
0.60
0.57
0.54
0.51
0.49
0.46
0.43
0.39
1.22
1.11
1.02
0.96
0.92
0.84
0.77
0.72
0.67
0.62
0.60
0.56
0.53
0.51
0.48
0.44
0.40
1.26
1.15
1.06
1.00
0.95
0.87
0.80
0.75
0.70
0.65
0.62
0.55
0.58
0.53
0.50
0.46
0.42
Air Temp F
40
0
40
70
100
150
200
250
300
350
400
450
500
550
600
700
800
20.58
280.10
10000
21.39
291.10
9000
22.22
302.10
8000
23.09
314.80
7000
23.98
326.40
6000
24.90
333.90
5000
25.84
351.7
4000
26.82
365.00
3000
27.82
378.60
2000
28.86
392.80
1000
29.92
407.50
Sea
Level
Barometer (in. of
Hg.)
(in. w.g.)
Altitude (ft)
Table C-2: Air Density Correction Factors (U.S. Units) Standard Air Density (Sea Level and 70F) = 0.075 lb/ft3 at 29.92 in. Hg.
C.5
APPENDIX C
TAB ENGINEERING
C.5.1 TRAVERSE CALCULATIONS

The purpose of this section is to perform a sample duct traverse layout and perform a sample airflow
calculation.
Traverse measurements are performed in order to calculate the airflow volume (m/s or cfm) flowing
inside of a duct from actual field measurements. The airflow volume is a function of two components:
the cross sectional area of the duct (m or ft) and the velocity of the air (m/s or fpm) flowing inside
that duct. Equation C.5.1 identifies the relationship.
Equation C.5.1
Q=VxA
where: Q = Airflow Volume (m/s or cfm)

V = Velocity (m/s or fpm)
A= Cross-sectional area of the traverse plane (m or ft)
Measurements of airflow velocity are usually performed with a manometer and a Pitot tube. An
analog manometer will provide measurements in units of velocity pressure (Pa or in. w.c). Velocity
pressure measurements can be converted to units of velocity using Equation C.5.2.
Equation C.5.2 (SI): V = 1.414 (VP/d)
where: V = Velocity in m/s
VP = Velocity pressure in Pa
D = Density in kg/m
or, for Standard Air (d = 1.204 kg/m3)
V = (1.66 VP)
Equation C.5.2 (IP): V = 1096 (VP/d)
where: V = Velocity in fpm
VP = Velocity pressure in in. w.c.
D = Density in lbs/ft
or, for Standard Air (d = .075 lbs/ft3)
V = 4005 (VP)
Digital manometers also measure velocity pressure and automatically perform the conversion and
display the velocity value directly. In either case, the important feature to note is that individual
velocity pressures shall be converted to individual velocities and then averaged to obtain the average
airflow velocity in the duct.
NOTE: Because the velocity varies directly as the square root of velocity pressure, it is
incorrect to simply average the velocity pressures and then make one conversion to velocity.
Regardless of the type and size of duct insulation (none, lined, or wrapped), the shape of the duct, or
materials of construction, there are several uniform concepts that apply to all duct traverse
measurements and calculations:
XIX
APPENDIX C
1. The cross sectional area and the shape of the duct at the location of traverse plane shall be
uniform. The traverse plane should not be located in a transition.
2. The traverse plane should be located in a straight run of duct, sufficiently upstream and
downstream of elbows, transitions, obstructions, equipment, fans, etc.
3. The direction of the air stream should be at right angles to the traverse plane and the Pitot
tube position should be within 5 of perpendicular to the traverse plane at the maximum
velocity pressure.
4. No readings shall be less than zero.
5. An accuracy of 10% is usually achieved when 75% of the velocity pressure readings are
greater than 0.10 of the maximum velocity pressure reading.
There are two methods for traverse layouts in rectangular ducts: the Equal Area Method and the Log
Tchebycheff Rule (named after the Russian physicist who created the method) or more simply, the
Log T Method. Either layout method is acceptable. Duct traverse layouts in round ducts follow a
method known as Log Linear. Finally, there are referenced traverse layouts for flat oval duct also.
Examples of layouts and the requirements for round ducts, flat oval ducts, or either the Equal Area or
the Log T method for rectangular ducts can be found in the current edition of the NEBB Testing
Adjusting Balancing Manual for Technicians.
C.5.2 SAMPLE TRAVERSE LAYOUT AND AIRFLOW CALCULATION
The traverse layout and calculations presented in this example are intended to serve as a working
illustration of the correct procedures and methods involved in determining airflow volume in a duct. For
this example we have a 750 mm x 450 mm (26 X 14) OD duct that is lined with 25 mm (1) of
fiberglass insulation. You are required to layout an Equal Area Traverse, take the appropriate velocity
pressure measurements, and determine the actual airflow volume flowing in the duct. According to
NEBB requirements, an Equal Area Traverse is to have a minimum of 16 readings with a maximum
spacing of 150 mm (6) between readings. The maximum number of readings is 64. After 64 readings
the center-to-center distance may be increased accordingly. Each reading is to be located in the center
of each equal area duct section.
Solution: The Equal Area Method creates equal area sections inside the duct opening. It is only
concerned about the internal, or inside, dimensions of the duct. Our duct in this example has an
outside dimension of 750 mm x 450 mm (30 X 18), but the inside free area is 700 mm by 400 mm (28
x 16). So, we need to layout a minimum of 16 equal are sections within the 700 mm x 400 mm (28 x
16) opening.
For this example, we have selected to perform a traverse with 7 sets readings across the bottom of the
duct and 4 sets of reading down the vertical side. This would produce a 7x 4 averaging grid, or 28
points of measurement. That exceeds the minimum requirement of 16 readings which is acceptable.
Additionally, each equal area section is 100 mm x 100 mm (4 x 4) and the location of each
measurement point is exactly centered in the middle of each equal are section. Other traverse layouts
are acceptable as long as the minimum number of points is 16 and the maximum spacing is followed.
XX
APPENDIX C
The solution is shown in Figure C.5.1 below:
FIGURE C5.1
Assuming we have now correctly laid out the traverse point grid, the actual velocity pressure
measurements are made. Table C-3 identifies the field measurements.
Table C-3 (SI) Velocity Pressure Measurements (Pa)
Location
1
2
3
4
1
8
14
16
14
2
9
19
17
14
3
9
19
18
17
4
10
20
19
17
5
11
21
14
13
6
11
16
13
11
7
8
10
10
11
5
0.044
0.084
0.056
6
0.044
0.064
0.052
7
0.032
0.040
0.040
Table C-3 (IP) Velocity Pressure Measurements (in. w.c.)

Location
1
2
3
1
0.032
0.056
0.064
2
0.036
0.076
0.068
3
0.036
0.076
0.072
4
0.040
0.080
0.076
XXI
0.056
0.056
0.068
APPENDIX C
0.068
0.052
0.044
0.044
As previously mentioned, each velocity pressure must now be converted to individual velocities and
then the individual velocities are averaged. Table C-4 has converted each velocity pressure to velocity.
Table C-4 (SI) Velocity Measurements (m/s)
Location
1
2
3
4
1
3.69
4.78
5.16
4.78
2
3.95
5.62
5.30
4.78
3
3.95
5.62
5.52
5.30
4
4.08
5.75
5.62
5.30
5
4.27
5.84
4.78
4.64
6
4.27
5.16
4.64
4.27
7
3.69
4.08
4.08
4.27
4
801
1133
1104
1044
5
840
1161
948
913
6
840
1013
913
840
7
716
801
801
840
Table C-4 (IP) Velocity Measurements (fpm)

Location
1
2
3
4
1
716
948
1013
948
2
760
1104
1044
948
3
760
1104
1075
1044
The average velocity can now be calculated by adding all of the individual velocities and dividing by the
total number of readings. The average velocity is 5.15 m/s (1014 fpm). The total airflow volume in the
duct can now be determined by using Equation C.5.1
Equation C.5.1 (SI)
Q=VxA
Q = 5.15 m/s x (700 mm x 400 mm)/ 1,000,000 = 1.44 m/s
Equation C.5.1 (IP)
Q = 1014 fpm x (28 x 16)/ 144 = 3154 cfm
Comparing the metric to IP values is not an exact conversion as 1.00 m/s should equal 2119 cfm.
The reason this sample calculation did not come out to the exact value is that we used soft
conversions in length, area, velocity and velocity pressure. 700 mm is exactly 27.56, not 28. The
purpose of the example was not to demonstrate metric to IP conversions but rather to demonstrate
the correct procedure to layout a duct traverse, take the correct velocity pressure measurements,
convert the measurements to individual velocities, obtain an average velocity and then finally
determine the actual airflow volume in the duct.
C.6 STATISTICAL FORMULA AND EXAMPLES

C.6.1 95% UPPER CONFIDENCE LIMIT (UCL) CALCULATIONS
In calculating the 95% upper confidence limit, you must first calculate the average particle concentration.
After determining the average particle calculations, you must then calculate the mean of the averages.
The standard deviation can then be calculated using the mean of the averages. After determining the
standard deviation, the standard error may be determined. Then finally, the 95% upper confidence limit
may be calculated. This procedure is only required if you take less than 10 sample locations.
Average Particle Concentration
XXII
APPENDIX C
The average particle concentration (A) at a sample location is the sum of the individual sample particle
counts (C1) divided by the number of samples taken at the location (N), as shown in Equation C.6.1. If
only one sample is taken, it is the average particle concentration.
Equation C.6.1
A = (C1 + C2 + ... + CN) / N
C.6.1.1 Mean of the Averages
The mean of the averages (M) is the sum of the individual averages (A1) divided by the number of
locations (L), as shown in Equation C.6.2. All locations are weighted equally regardless of the number
of samples taken.
Equation C.6.2
M = (A1 + A2 + ... + AL) / L
C.6.1.2 Standard Deviation
The standard deviation (SD) of the averages is the square root of the sum of the squares of differences
between each of the individual averages and the mean of the averages (A1M)2 divided by the number
of locations (L) minus one, as shown in Equation C.6.3.
Equation C.6.3
(A1 M )2 + (A 2 M )2 + ... + (A L M )2
SD =
L 1
C.6.1.4 Upper Confidence Limit (UCL)
The 95 percent UCL of the mean of averages (M) is determined by adding to the mean the appropriate
UCL factor (see Table C-5 for UCL factor) times the standard error (SE), as shown in Equation C.6.5.
Equation C.6.5
UCL = M +
UCLFactorxSD
L
Note: This statistical analysis deals only with random errors (lack of precision), not errors of a
nonrandom nature ("bias"), such as erroneous calibration.
TABLE C-5 UCL Factor for 95 Percent Upper Confidence Limit

No. of Locations (L)
95 percent UCL factor
>9*
NA
6.3
2.9
2.4
2.1
2.0
1.9
1.9
1.9
NR
XXIII
APPENDIX C
*When the number of locations is greater than 9, the calculations of a UCL is not required (NR).
*When the number of locations is only one, the calculation of a UCL does not apply (NA).
C.6.2 RESULT INTERPRETATION OF DATA STATISTICAL ANALYSIS
C.6.2.1 Acceptance Criteria
The cleanroom or clean zone shall meet the acceptance criteria for an airborne particulate cleanliness
class if:
a.
b.
c.
the average of the particle concentration (see Table 10 1) measured at each location
falls at, or below, the class limit, and
if only one sample location is used, then the 95% UCL does not apply.
the total number of locations sampled is less than ten, the mean of these averages
must fall at or below the class limit with a 95 percent confidence limit.
C.6.2.2 Outliers
If the results are non-compliant due to a single outlier value, (due to procedural error or equipment
malfunction), it does not need to be included in the analysis provided that the calculation is repeated,
and at least three measurements values remain in the calculation
C.6.3 Example Calculation #1 (Cleanliness Classification Tests Calculation Procedure)
The data and calculations presented in this example calculation are intended to serve as a working
illustration of the statistical procedures involved in determination of acceptance criteria for cleanrooms
and clean zones. The data and calculations are based upon a 28.3 Liters (1 cubic foot) sample volume
and testing at 0.3 m measured particle size for ISO Class 4.
Particle counts have been taken in a cleanroom. The number of particle counts, the actual sample
counts and the number of sample locations is presented in Table C-7.1. The Owner has stated the
cleanroom classification is an ISO Class 4 room at 0.3 m. Calculate the 95% UCL and determine if the
cleanroom meets that cleanliness classification.
TABLE C-7.1 Tabulation of Particle Count Data
Particle Counts (C1)
Location
744
1010
A
NR
989
B
334
765
C
NR
868
D
1050
799
E
(NR no reading taken)
557
633
NR
454
455
697
455
544
988
NR
NR
NR
333
999
NR
Total
No. of
(C1)
Total
(A1)
Average
Samples (N)
Count
Counts
4
3
4
4
3
C.6.3.1 Average Particle Concentration

As stated above, the average particle concentration (A) at a location is the sum of the individual sample
particle counts (C1) divided by the number of samples taken at the location (N), as shown in Equation
C.6.1. If only one sample is taken, it is the average particle concentration.
XXIV
APPENDIX C
Equation C.6.1
A = (C1 + C2 + ... + CN) / N, Thus:
A1= (1010 + 744 + 557 + 697) / 4
A2= (989 + 633 + 455) / 3
A3= (765 + 334 + 544 + 333) / 4
A4= (868 + 454 + 988 + 999) / 4
A5= (799 + 1050 + 455) / 3
= 3008/4 = 752.0
= 2077/3 = 692.3
= 1976/4 = 494.0
= 3309/4 = 827.3
= 2304/3 = 768.0
This data can now be inserted into its appropriate space in the table and the completed table is shown
in Table C-7.2.
TABLE C-7.2 Tabulation of Particle Count Data
Total
No. of
(C1)
Total
(A1)
Average
Samples (N)
Count
Counts
4
3
4
4
3
3010
2077
1976
3309
2304
752.0
692.3
494.0
827.3
768.0
Particle Counts (C1)
Location
A
B
C
D
E
1010
989
765
868
799
744
NR
334
NR
457
557
633
NR
454
455
697
455
544
988
NR
NR
NR
333
999
NR
C.6.3.2 Mean of the Averages

The mean of the averages (M) is the sum of the individual averages (A1) divided by the number of
locations (L), as shown in Equation C.6.2. All locations are weighted equally regardless of the number
of samples taken.
Equation C.6.2
M = (A1 + A2 + ... + AL) / L, Thus:
M = (752.0 + 692.3 + 494.0 + 827.3 + 768.0)/5 = 706.1
The standard deviation (SD) of the averages is the square root of the sum of the squares of differences
between each of the individual averages and the mean of the averages (A1M)2 divided by the number
of locations (L) minus one, as shown in Equation C.6.3:
Equation C.6.3
SD =
( A1 M )2 + ( A2 M )2 + ... + ( AL M )2
L 1
Thus:
XXV
SD =
SD =
APPENDIX C
(752.5 706.1)2 + (692.3 706.1)2 + (494.0 706.1)2 + (827.3 706.1)2 + (768.0 706.1)2
5 1
(46.4)2 + ( 13.8)2 + ( 212.1)2 + (121.2)2 + (62.1)2

5 1
= 128.33
C.6.3.4 Standard Error

The standard error (SE) of the mean of the averages (M) is determined by dividing the standard
deviation (SD) by the square root of the number of locations, as shown in Equation C.6.4.
Equation C.6.4
SE =
SD
L
Thus,
SE =
128.33
5
= 57.4
C.6.3.5 Upper Confidence Limit (UCL)

The 95 percent UCL of the mean of averages (M) is determined by adding to the mean the appropriate
UCL factor (see Table C-5 for UCL factor) times the standard error (SE), as shown in Equation C.6.5.
Equation C6.5
UCL = M + (UCL factor SE )

UCL = 706.1 + (2.13 57.4 ) = 828.36
C.6.3.6 Summary
As stated above, the cleanroom or clean zone shall meet the acceptance criteria for an airborne
particulate cleanliness class if:
a. the average of the particle concentration (see Table 10 1) measured at each location falls at, or
below, the class limit, and
b. if only one sample location is used, then the 95% UCL does not apply.
c. the total number of locations sampled is less than ten, the mean of these averages must fall at or
below the class limit with a 95 percent confidence limit
Conclusion
XXVI
APPENDIX C
For this example calculation, the 95% UCL is 828.36. The Owner has stated that the cleanrooms
cleanliness classification is an ISO Class 4 at 0.3 m. From Table 10-1, the class limit for these
conditions is 1020 particles per cubic meter. Since the upper 95 percent confidence limit (UCL) is less
than 1020 particles per cubic meter and all location average particle concentrations (A1) were less than
1020 particles per cubic meter, the above data meet the acceptance criteria for an ISO Class 4 at 0.3
m. Even though one or more of the individual particle counts is above 1020 particles per cubic meter,
the room still passes the acceptance criteria.
C.6.4 Sample Calculation for Uniformity (Applies to Airflow Velocity Uniformity Tests, Airflow
Volume Uniformity Tests, Temperature and Humidity Uniformity Tests and Lighting Level
Uniformity Tests)
This calculation procedure is performed when taking 5 or more data points to determine the uniformity of
the data. The method described is applicable to all of the uniformity tests, such as velocity, volume,
temperature and humidity, lighting levels, and sound levels.
The data and calculations presented in this example calculation are intended to serve as a working
illustration of the statistical procedures involved in determination of the relative standard deviation. For
this example, airflow volumes readings have been taken at 5 HEPA filters. The results are identified in
Table C-8.
TABLE C-8 Tabulation of Airlfow Volume Data
HEPA Filter
Measured
Volumes (cfm)
710
725
690
701
744
Average
714.0

The standard deviation (SD) of the readings is the square root of the sum of the squares of differences
between each of the individual readings and the average reading (A1M)2 divided by the number of
locations (L) minus one, as shown in Equation C.6.3:
Equation C.6.3
SD =
SD =
( A1 M )2 + ( A2 M )2 + ... + ( AL M )2
L 1
Thus:
(710 714 )2 + (725 714 )2 + (690 714)2 + (701 714) 2 + (746 714) 2
5 1
XXVII
SD =
SD =
APPENDIX C
( 4 )2 + (11)2 + ( 24 )2 + ( 13)2 + (32 )2

5 1
(16 ) + (121) + (576 ) + (169 ) + (1024 )
SD =
1096
= 16.55
4
C.5.4.2
Relative Standard Deviation
The relative standard deviation is standard deviation divided by the average and is shown is Equation
C.6.6.
Equation C.6.6
RSD =
SD
M
RSD =
16.55
= 0.02318 = 2.32%
714
C.7 SCAN RATE DETERMINATION AND EXAMPLE

C.7.1 Example Scan Rate
Section 10.13 details the requirements to perform the Filter Installation Leak Tests Discrete Particle
Counter Test Method. Section 10.13.2.4 identifies the formula to calculate the Acceptable Scan Rate (Sr).
The formula is re-stated below as Equation C.7.1.
The following example details the procedure. You need to determine the scan rate for a HEPA Filter
Installation Leak Test using a discrete particle counter. The upstream concentration is 106,007 particles
per liter. The probe dimension is 1.27 cm parallel to the scan direction. The number of particles that
indicate a significant leak is 3.0. The sample flow rate is 28.3 lpm. The significant leak percentage is
0.01%. Scanning shall be done isokinetically.
Solution: Use Equation C.7.1 to determine the appropriate scan rate.
Equation C.7.1
Where:
Sr
=
Cc
=
Cc x Ls x Fs x Dp
Sr = -----------------------------------60 x Np
Acceptable Scan Ratecm/s (in/s)

Upstream challenge concentrationparticles/L (particles/ft3)
XXVIII
Ls
Fs
Dp
Np
60
=
=
=
=
=
APPENDIX C
Significant leakpercentage of upstream concentration (typically 0.01%)

Sample flow rate of instrument usedL/m (cfm)
Probe dimension parallel to scan directioncm (inches)
conversion60 sec/min
Inserting the known data would yield:

Cc
Ls
Fs
Dp
Np
60
=
=
=
=
=
=
106,007 ppl (3,000,000 ppcf)

0.01% (0.0001)
28.3 lpm (1.0 cfm)
1.27 cm (0.50 in)
3.0 Number of particle counts that indicate the leak
Thus Equation C.7.1 (SI) becomes:
Sr =
106,007 0.0001 28.3 1.27

= 2.1167cm / sec
60 3
or, Equation C.7.1 (IP) becomes:
Sr =
3,000,000 0.0001 1.0 0.5

= 0.833in / sec
60 3
If a lower value of Np is used (1) the allowable scan rate will be increased but the probability of finding a
leak will be decreased. If a larger Np is used (10) the allowable scan rate is decreased but the
probability of detecting a leak is increased.
C.8 PARALLELISM ANGULAR OFFSET FROM TRUE VERTICAL

DETERMINATION AND EXAMPLE
C.8.1
ANGULAR DETERMINATION
The Airflow Parallelism Test requires that the angular offset of the airflow be determined. To determine
the angular offset angle from true vertical as required by the Airflow Parallelism Test, use Equation C.8.1
and Figure C.8.1.
XXIX
APPENDIX C
a
Figure C.8.1
Equation C.8.1
angle A = tan-1 (a/b)
Where:
A
=
Angular offsetdegrees
a
=
Deflection distancemm (inches)
b
=
Vertical heightmm (inches)
Table C-9 provides the tangent value and angle of some pre-calculated offsets.
TABLE C-9: Airflow Parallelism Test Angles

Tangent
0.070
0.105
0.141
0.176
0.213
0.249
0.287
0.325
Angle A
4
6
8
10
12
14
16
18
C.8.2 ANGULAR DETERMINATION EXAMPLE

The Airflow Parallelism Test requires that the airflow can not deflect more than 14 from true vertical as
it is discharged from the air outlets. Field measurements have indicated the following measurements:
a = 369 mm (14.50 inches) and b = 1829 mm (72.00 inches).
Determine if the airflow meets test criteria.
Solution:
Equation C.8.1
angle A = tan-1 (a/b)

angle A = tan-1 (369/1829)
XXX
APPENDIX C
angle A = 11.4, The test passes because the angle of deflection of the
airflow is less than 14 from true vertical.
C.9 FILTER INSTALLATION LEAK TESTS AMBIENT PARTICULATE TEST

METHOD
This test is not recommended by NEBB. It is not to be considered an alternate equal to the either of the
methods described Section 10.11 or Section 10.12. The reason that this test is not recommended by
NEBB is due to the low upstream particle concentrations normally found in re-circulated air from
cleanrooms. Typical users of this test are unable to locate significant leaks. Scan rates as calculated in
Section 10.12 would be excessive. See the following example that is based on an airflow velocity of
0.51 m/s (100 fpm).
Example C.9.1
Cc
Ls
Fs
Dp
Np
60
=
=
=
=
=
=
1,767 particles/L (50,000 particles/ft3)

0.01% (0.0001)
28.3 L/min (1.0 cfm)
1.27 cm (0.50 in)
Equation 10-3 (SI)
Equation 10-3 (IP)
1767 x 0.0001 x 28.3 x 1.27

Sr = -----------------------------------60 x 1
= 0.1058 cm/s
50,000 x 0.0001 x 1.0 x 0.50

Sr = -----------------------------------60 x 1
= 0.0417 in/s
Thus it would take 172.8 minutes to completely scan a 610 mm x 1220 mm (2 ft x 4 ft) filter. If a lower
value of Np is used, such as 1, the allowable scan rate will be increased but the probability of finding a
leak will be decreased. If a larger Np is used, such as 10, the allowable scan rate is decreased but the
probability of detecting a leak is increased. For these reasons, NEBB does NOT recommend this test
method.
C.10 SAMPLE AIR CHANGE RATE PER HOUR (ACH) CALCULATION

The following is an example of the procedure to be utilized when trying to determine the number of air
changes per hour (ACH) that exist within a cleanroom or space. While the ACH provides a value as
to the number of complete air changes occurring within a location, it is NOT an indicator as to the
quality of the air or the effectiveness of the exchange rate. It is simply a mathematical relationship.
XXXI
APPENDIX C
In order to determine the ACH, the room volume and the air total airflow within the space must be
identified.
The formula for determining ACH is identified in Equation C-10.1 below.
Equation C-10.1 (SI): Air Change Rate per Hour (ACH)
ACH = Q / V
Where: Q = Airflow m /hr
V = Volume m
Equation C-10.1 (IP): Air Change Rate per Hour (ACH)

ACH = (Q 60) / V
Where: Q = Airflow ft /min
V = Volume ft
60 = minutes/hour
A final comment pertaining to air change rate relates to which airflow rate is used; total supply airflow
or total return/exhaust airflow. Older conventions based the ACH on the supply airflow only
regardless if the room was being maintained at a positive or negative pressure. Current thinking
utilizes the total supply airflow rate for positively pressurized spaces and the total return/exhaust
(which would include the total supply plus any infiltration) for negatively pressurized spaces.
C.11 CALCULATION OF Kv FACTOR TO DETERMINE AIRFLOW VOLUME

FROM AVERAGE AIRFLOW FACE VELOCITY
The following procedure should be used when trying to determine a Kv factor. The Kv factor is used in
determining the airflow volume from average airflow face velocity.
Select a standard filter that is accessible with the flow-hood. Take several (at least 2) readings to
obtain a representative average airflow.
Divide airflow volume (L/s, M3/m or s, cfm) by the effective filter area. The effective area is the actual
area of the filter medium through which air is passing.
Measure the airflow velocity from the same filter using an instrument as listed in Section 4.
Average the readings to obtain average filter velocity.
Divide the actual filter velocity by the measured filter airflow to obtain the Kv factor by using Equation
C-11.1.
XXXII
APPENDIX C
Equation C-11.1: Kv Factor:
Where: Kv = correction factor

Qa = Actual volumetric flow rate
Ae = Effective filter area
Vm = measured filter airflow velocity
Measure the inaccessible filter with the same velocity measuring instrument.
Multiply the average measured velocity by the Kv factor as calculated above to obtain actual filter
velocity. Multiply the actual airflow velocity by the effective filter area to obtain equivalent volumetric
flow rate.
XXXIII
XXXIV
APPENDIX C

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PROCEDURAL

2009 THIRD EDITION

PROCEDURAL STANDARDS FOR CERTIFIED

Copyright NEBB, 2009

CLEANROOM COMMITTEE MEMBERS

SECTION 2 NEBB Program, Quality Control and Compliance

SECTION 4 Standards for Equipment, Instrumentation

NEBB CPT PROCEDURAL STANDARDS

SECTION 5 Standards for Reports and Forms

NEBB CPT PROCEDURAL STANDARDS

SECTION 7 Cleanroom Safety

SECTION 8 Cleanroom Protocol

NEBB CPT PROCEDURAL STANDARDS

SECTION 10 Primary Tests

NEBB CPT PROCEDURAL STANDARDS

SECTION 11 Secondary Tests

NEBB CPT PROCEDURAL STANDARDS

NEBB CPT PROCEDURAL STANDARDS

Sample CPT Specifications

APPENDIX A-1 Sample CPT Specification Microelectronics &

References and Referenced Publications

Engineering Formulas, Equivalents, & Examples

NEBB CPT PROCEDURAL STANDARDS

NEBB CPT PROCEDURAL STANDARDS

Classification: A specified level of airborne particulate cleanliness applicable to a cleanroom or clean

Any circumstance that adversely affects the specified performance of a device or

NEBB CPT PROCEDURAL STANDARDS

Filter Face Velocity:

A nozzle used for the generation of a heterogeneous DOP or PAO aerosol by

Leak: Penetration of contaminates that exceed an expected value of downstream concentration

NEBB CPT PROCEDURAL STANDARDS

NEBB CPT PROCEDURAL STANDARDS

NEBB CPT PROCEDURAL STANDARDS

SECTION 2 - NEBB PROGRAM,

Cleanroom Performance Testing (CPT)

NEBB CPT PROCEDURAL STANDARDS

2.2 QUALITY ASSURANCE PROGRAM - CONFORMANCE CERTIFICATION

2.3 QUALITY CONTROL AND COMPLIANCE

NEBB CPT PROCEDURAL STANDARDS

2.4 CERTIFIED CPT PROFESSIONAL RESPONSIBILITIES

NEBB CPT PROCEDURAL STANDARDS

3.2 OWNER / BUYER AND DESIGN AND CONSTRUCTION TEAM

NEBB CPT PROCEDURAL STANDARDS

3.2.2 OWNER / BUYER AND / OR CONSTRUCTION TEAM RESPONSIBILITIES

Complete the installation, programming (including design parameters and graphics),

3.2.3 NEBB CERTIFIED CPT FIRM RESPONSIBILITIES

NEBB CPT PROCEDURAL STANDARDS

NEBB CPT PROCEDURAL STANDARDS

SECTION 4 - STANDARDS FOR

4.2 RANGE AND ACCURACY

NEBB CPT PROCEDURAL STANDARDS

TABLE 4-1 NEBB MINIMUM INSTRUMENTATION REQUIREMENTS

A digital manometer capable of meeting

A tube array with the following:

Range: 0.13 12.5 m/s (25 to 2500 fpm)

Airflow Volume and Uniformity Test

A flow capture hood with an integral

Airflow Volume and Uniformity Test

A digital manometer capable of meeting