STD-02-0860 Rev 5.0 Part Cleanliness Standard
STD-02-0860 Rev 5.0 Part Cleanliness Standard
STD-02-0860 Rev 5.0 Part Cleanliness Standard
1.0 Purpose
This standard applies to all engine ready components, where the relevant
requirements are stated in the specification, and replaces all other cleanliness
requirements. In the event of a conflict between this standard and any references
cited, this standard shall take precedence. This standard does not apply to cast
blanks or in-process components. Parts as purchased shall meet the visual
cleanliness of JWN 890110 / P23E-AL-0255 and residual magnetism requirements of
STD-02-0864 or associated RAIP.
3.0 Definitions
Acronym Meaning
None None
4.0 Procedure/Requirements
Table 1: Cleanliness degree for mass – relevant for all dirt contamination
Total particle mass (mg / 1000 cm2)
DP cleanliness class All sizes inclusive of the residual dirt mass
1 n/a
2 5
3 20
4 50
5 200
6 N/A
Table 2: Cleanliness degree for particle quantity and size – only relevant for metallic
contamination
Particle size (number of particles / 1000 cm2)
Class E F G H I J K L M
as per
VDA
19
Size 50≤ x 100≤ 150≤ 200≤ 400≤ 600≤ 1,000≤ 1,500≤ x
Class <100 x x x x x x x ≥2,000
[μm] <150 <200 <400 <600 <1,000 <1,500 <2,000
Cleanlin 1 Class 1: see Table 3
ess no no
Class 2 100 20 3 0 0 0 0
limit limit
no no no
3 100 20 5 0 0 0
limit limit limit
no no no no
4 150 30 20 0 0
limit limit limit limit
no no no no no
5 150 30 10 0
limit limit limit limit limit
no no no no no
6* 250 50 25 0
limit limit limit limit limit
*Values applicable only in case of measurement. Measurement required only in case of
specific request. Otherwise, parts are only required to be “Visually Clean” as defined in this
standard.
Table 3: Cleanliness class 1 – cleanliness by component type – only relevant for metallic
contamination
Component Reference Permissible particle value for different size classes [μm]
0≤ x 25≤ x 50≤ x 100≤ x 200≤ x x non-
<25 <50 <100 <200 <400 <400 metallic
High-pressure 3.1 no record 85 12 0 0 record
injector limit only only
High-pressure 3.2 no record 200 25 0 0 record
safety valve limit only only
High-pressure 3.3 no record 200 20 5 0 record
fuel pump limit only only
High-pressure 3.4 no record 50 6 0 0 record
fuel line limit only only
High-pressure 3.5 no record 150 40 5 0 record
inlet measuring limit only only
valve
High-pressure 3.6 no record 180 30 7 0 record
terminal box limit only only
Components must be visibly free from loose particles to the human eye. If the critical
area is not visible, use suitable equipment (e.g. an endoscope) to evaluate it.
Components must be free from rust, swarf, abrasion or loose particles.
Forgings and castings must not show any residual rust, erosion, steel grit, nicks or
burrs. More precise details are set out in the relevant specification.
All purchased parts must be packaged by the supplier in conformance with JWN
890110 / P23E-AL-0255, and parts subject to this standard shall be packaged to
maintain the specified cleanliness for 3 months after receipt. The end and/or other
openings of tubing, fittings, pipe, and elbows subject to this standard shall be
packaged with barrier protection to ensure cleanliness of interior surfaces.
Absence of a cleanliness notation on the drawing does not exclude apart from this
standard. Drawings that do not have a cleanliness callout must be addressed with
SQE and Engineering prior to shipment of parts.
The inspection facility must be suitable for the inspection to be conducted (see VDA
19). Evidence of the suitability must be documented in the form of a blank value (as
described in VDA 19). The inspection of technical cleanliness is usually conducted in
a monitored environment similar to a clean room (minimum: ISO 14644, Class 8). It
must be secured on site (clean room) or mechanically (closed cleanliness cabinet).
4.5 Extraction:
The extraction method selected is spraying (as described in VDA 19). The extraction
parameters must be determined by decay measurement (as described in VDA 19).
This qualification measurement must be prepared as evidence of the suitability of the
inspection method and documented in the form of an inspection specification.
Geometrically similar components can be grouped into component families and
inspected on the basis of an inspection specification.
4.6 Analysis:
Weighing scales with a 0.1 mg resolution must be used for the gravimetric analysis.
The progress of the procedure is described in VDA 19.
The numerical analysis of the filters requires at least one computerized, photo-optical
system capable of distinguishing metallic from non-metallic shiny particles (see VDA
19).
4.7 Quality:
A process control plan shall be in place for final wash systems for core critical parts,
crankcase, crankshafts, connecting rods, cylinder heads and pistons, and for all parts
with cleanliness designated as a key design feature on the part drawing.
4.8 Documentation:
The results are documented in an inspection report containing at least the following
information:
Header data:
• Inspection date
• Part No.
• Component description
• Cleanliness class in accordance with JWN 890 115 / STD-02-0860
• Inspection facility used
• Component surface inspected [cm²]
• Associated blank value, if any
Extraction parameters:
• Method used
• Batch size
• Description of rinsing medium
Analysis parameters:
• Microscope scale/resolution [μm/pixels]
• Evaluation diameter [mm]
• Largest metallic shiny particle (Feretmax) [μm]
• Measured values in accordance with JWN 890 115 / STD-02-0860
• Test result
4.9 Miscellaneous
The procedure for monitoring technical cleanliness must be checked and approved
by an SQE in collaboration with the GSCM quality department.
As a rule, cleanliness limits represent control limits and not tolerance limits. A limit
which has been exceeded does not result directly in a fault but increases the risk of
one. If a component is identified during a technical cleanliness inspection as
exceeding the limits referred to above, then a Non-Conformance (NC) will be created.
This NC is to be reviewed by applicable Quality and Engineering teams for
acceptability and/or corrective action. If rejected, the non-millipored parts are to be
sent out for re-cleaning and supplier/manufacturer will need to resubmit for Millipore
qualification, as per the quality management system.
5.1 Responsibilities
6.0 References