Agilent Katalog 2009 en
Agilent Katalog 2009 en
Agilent Katalog 2009 en
Inlets ..........................................................................................................45
Premium Non-Stick Septa.........................................................................................................................................................46
Ferrules .....................................................................................................................................................................................50
Capillary Flow Technology Supplies..........................................................................................................................................54
Split/Splitless Liners ..................................................................................................................................................................55
Direct Connect Liners................................................................................................................................................................59
Helix Liners................................................................................................................................................................................59
Split/Splitless Inlets...................................................................................................................................................................60
Cool On-Column Inlets ..............................................................................................................................................................69
Purged Packed Inlets ................................................................................................................................................................75
Programmed Temperature Vaporizer (PTV) Inlets .....................................................................................................................78
Detectors ...................................................................................................83
Flame Ionization Detector (FID)................................................................................................................................................84
Electron Capture Detector (ECD)..............................................................................................................................................91
Thermal Conductivity Detector (TCD) .......................................................................................................................................94
Flame Photometric Detector (FPD)...........................................................................................................................................99
Nitrogen Phosphorus Detector (NPD) ....................................................................................................................................106
Nitrogen and Sulfur Chemiluminescence Detectors...............................................................................................................113
Moisture
• Can be introduced by improper handling and/or installation of plumbing.
• A common cause of column stationary phase degradation.
• Can damage instrument.
Oxygen
• Most common contaminant.
• A common cause of column stationary phase and inlet liner degradation.
• Can cause decomposition of labile analytes.
• Opportunity for introduction at every fitting present in the gas line or during
use of gas permeable tubing.
1 = Moisture Trap
FID make-up, air, and H2
2 = Hydrocarbon Trap
Silica Gel, Grade 40, and Indicating Silica Gel, Grade 48 (MT-S Series)
Refillable 120 31.5 40 MT120-2-S MT120-4-S
Moisture Trap
Refillable 200 52.5 39 MT200-2-S MT200-4-S
Moisture Trap
Refillable 400 105.0 39 MT400-2-S MT400-4-S
Moisture Trap
Refillable glass moisture trap
Adsorbent Refill (1 pint) for MT-S series SGR SGR
Hydrocarbon Traps
Hydrocarbon traps remove organics,
such as hydrocarbons and halocarbons,
from the gas stream. The adsorbent is
usually activated carbon or an impregnated
carbon filter media. Carbon removes
Hydrocarbon trap, HT200-2
organic solvents from the gas stream,
including the typical solvents used
in nearly every lab. Hydrocarbon-moisture
combination traps are also available which Hydrocarbon Traps
remove water in addition to organics.
Capillary grade hydrocarbon traps are Description Size 1/8 in. 1/4 in.
purged with ultra-high helium and packed (cc) Part No. Part No.
with a very efficient activated carbon
Hydrocarbon Traps (HT Series)
material. Metal trap bodies are used to
prevent any contaminants in plastic trap Hydrocarbon Trap 200 HT200-2 HT200-4
bodies from contaminating the carbon Adsorbent Refill (1 pint) ACR ACR
adsorbent. Most hydrocarbon traps
can be refilled by the end user. Big Hydrocarbon Traps (BHT Series)
Big Hydrocarbon Trap 750 BHT-2 BHT-4
Refill for Big Hydrocarbon Trap (enough for two refills) BACR BACR
Oxygen Traps
Description Size 1/8 in. 1/4 in.
(cc) Part No. Part No.
Combination Traps
Agilent carries several Combination Traps
that provide multiple contaminant removal
in a single trap. These traps offer:
• Optimized adsorbents for maximum
surface area and capacity.
Agilent OT3 trap
• Leak-free, one-piece design to eliminate
potential leaks from using multiple traps.
• Efficient design which prevents
Combination Traps
channeling and promotes
efficient scrubbing. Description Size 1/8 in. 1/4 in.
• The ultimate in purification with (cc) Part No. Part No.
the Big Universal Trap, which removes Oxygen/Moisture Traps (OT3 Series)
oxygen, moisture, hydrocarbons,
carbon monoxide, and carbon dioxide. OT3 Trap 100 OT3-2 OT3-4
Universal/external split vent trap with 3 cartridges, 1/8 in. Swagelock fitting RDT-1020
Replacement cartridges, 3/pk RDT-1023
Split vent trap kit G1544-60610
Brass Body, Dual Stainless Steel Diaphragms, 1/8 in., U.S. Only*
Description Part No.
CGA 580, 125 psig max (8.6 bar), He, Ar, N2 5183-4644
1/8 in. (A) x 1/4 in. (B) connector, brass (included with brass regulators) 1/ea 0100-0118
1/4 in. (A) x 1/4 in. (B) connector, brass* 1/ea 0100-0119
Tips & Tools *Required for plumbing 1/4 in. tubing to regulators
When ordering a regulator, be sure
to specify the proper connections.
In the US, most gas manufacturers
follow CGA connection guidelines.
In Europe, there are a number of
organizations designating cylinder
connections that are specific to
individual countries. It is best
to contact your local supplier for
the proper connection designation.
Tubing
Cleaning Tubing Agilent recommends using copper tubing for most applications, since it is easy to bend
and plumb and is less expensive than stainless steel. Use stainless steel tubing only for
Before any tubing is placed into service,
crucial applications that require very high purity, or where building codes mandate its use.
or if it becomes contaminated with use,
it is essential that it be properly cleaned.
Unclean or improperly cleaned tubing can Determining Tubing Length
lead to contamination of the system with
disastrous results. Never use chlorinated Parameters: 2000 sccm (4.2 scfh); Temperature: 70°F; Pressure 30 psig
solvents to clean tubing or fittings.
Tubing Type Diameter Recommended Pressure Drop
Agilent provides clean, high quality (inches) Max. Length (feet) (psig)
GC grade tubing for large systems as
an economical alternative. Copper 1/8 50 2
Copper 1/4* 300 0.5
*Recommended when multiple instruments are connected to the same source
Tubing - Precleaned
Description Part No.
Fittings
Description Part No.
ADM 1000
• Accuracy ± 3%.
• Operating temperature range – 0 to 45ºC for the instrument, -70 to 135ºC
for the tubing.
• Calibration – traceable to NIST primary standards.
• Real time, split ratio measurement.
• CE mark certified.
• Measures flow rates from 0.5 to 1000 mL/min.
• Split ratios – compare the ratio from one gas measurement to another
(i.e., injection port split ratios).
ADM flowmeters
ADM 2000
In addition to the features of the ADM 1000, the ADM 2000 includes:
• Mass flow measurements – measure flow rate, independent of atmospheric pressure
and temperature (calculated).
• Data output through RS-232 port.
• 9V battery and AC power adapter (120 or 220 VAC).
ADM Flowmeters
Description Flow Rate Gases Accuracy (%) Power RS-232 Part No.
(mL/min) Measured* Supply Data Output
Low High
Check valves, fittings, and traps for leaks after every maintenance and thermal
cycling, as these can loosen some types of fittings.
Check for leaks at these connections:
Vial Options
Vial Filling
When filling sample vials, keep in mind:
• If you need to test a large amount of sample over repeated injections, divide the sample
among several vials to obtain reliable results.
• When sample volume in the vial is low, contaminants from the previous sample
injection or solvent washes may have a greater impact on the sample.
The airspace in the vial is necessary to avoid forming a vacuum when sample
is withdrawn. This could affect reproducibility.
5 minimum 6.25
3.7
8.2
34.5 maximum
32
11.7
Microvial insert Crimp cap sample vial Maximum height of a capped vial
Type Uses
Convenience vial and cap pack Clear with write-on spot Blue screw caps, PTFE/red 500/pk 5182-0867
rubber septa
Amber with write-on spot Green screw caps, PTFE/red 500/pk 5182-0733
rubber septa
Clear Blue screw caps, 500/pk 5182-0736
PTFE/silicone/PTFE septa
Clear with write-on spot Blue screw caps, 500/pk 5182-0869
PTFE/silicone/PTFE septa
Amber with write-on spot Green screw caps, 500/pk 5182-0737
PTFE/silicone/PTFE septa
Clear Blue screw caps, PTFE/silicone 500/pk 5182-0734
septa
Clear with write-on spot Blue screw caps, PTFE/silicone 500/pk 5182-0868
septa
Amber with write-on spot Green screw caps, PTFE/silicone 500/pk 5182-0735
septa
Clear Blue screw caps, pre-slit 500/pk 5183-2079
PTFE/silicone septa
Clear with write-on spot Blue screw caps, pre-slit 500/pk 5183-2080
PTFE/silicone septa
Amber with write-on spot Green screw caps, pre-slit 500/pk 5183-2081
PTFE/silicone septa
Clear Blue screw caps, pre-slit 500/pk 5067-0205
PTFE/silicone septa
11 mm Electronic Crimper with 4.8v rechargeable battery pack and charger 5062-0207
20 mm Electronic Crimper with 4.8v rechargeable battery pack and charger 5062-0208
11 mm Electronic Decapper with 4.8v rechargeable battery pack and charger 5062-0209
20 mm Electronic Decapper with 4.8v rechargeable battery pack and charger 5062-0210
4.8v nickel metal hydride replacement battery 5188-6565
Needle tips
Tips & Tools
For highest productivity and
to minimize coring, use Agilent
Premium Non-Stick Inlet Septa
with Center Point Guide.
See page 46.
Cone tip Tapered needle
10 µL, PTFE-tipped • Less plunger binding than fitted • More expensive than fitted plunger • High sample throughput
plunger • PTFE-tipped syringes not available • Samples in polar solvents
• Replaceable plunger for reduced in 5 µL size • Dirty samples
repair cost • Gases and volatile samples
• Tight seal between plunger and barrel • Reactive samples
10 µL, fitted plunger • Most economical • Most accurate only for 1 µL and • General purpose syringe
• Most reliable fitted plunger syringe larger injections • Clean samples
• Less bending • Plunger not replaceable • Routine analysis
• Better for high viscosity samples
5 µL, fitted plunger • Most accurate for 1 µL injection • Thinnest plunger, can bend more • 1 µL injections
• No hardware modification needed for easily • Clean samples
0.5 µL • Not ideal for higher viscosity • Routine analysis
samples
• Plunger not replaceable
Bent plungers or stuck syringes • Particles such as dust, leftover samples, salts, • Try PTFE-tipped plunger syringe.
metal, or glass can fill the narrow gap between the • If the plunger's movement feels "gritty," remove the
plunger shaft and the inside wall of the barrel. plunger from the barrel, flush the shaft with
solvent, and wipe it dry with a lint-free cloth. Then,
carefully insert the plunger back into the barrel.
Finally, submerge the tip of the needle into a
container of solvent, and cycle the plunger to pull
the solvent into and out of the barrel.
• Never cycle the plunger in a dry syringe.
• Do not "mix & match" plungers and barrels.
• Always clean syringes after use immediately.
Bent needles • Improper needle alignment. • Use only Agilent autosamplers.
• Narrow-gauge needles (26 gauge) bend more They are precision-designed to ensure proper
easily than larger (23 gauge) needles. alignment with the Agilent inlet.
• Needles tend to bend when inserted into the • Use 23 to 26-gauge tapered needles to get the
sample vial - not the inlet port. This can be caused combined benefits of greater septa life and fewer
by septa that are too "tough." bent needles.
• If the needle has been slightly bent when mounted • Only use Agilent vials and septa.
in the autosampler - or when the syringe is
installed into the autosampler - then it is more likely
to bend further when it pushes through the septa
on the sample vial caps.
Blocked needles • Sample material or contaminants may be trapped Remove the plunger and use a second syringe to fill
inside the needle. the blocked syringe with solvent. Then, insert the
• The needle may not have been properly cleaned. plunger and gently push solvent through needle.
Important: Try to use a cleaning agent that is
appropriate for the contaminant. Common choices
are methanol, methylene chloride, acetontrile,
and acetone.
Rust • During normal use, the shaft rubs against the glass To slow this process, remove the water from the
Note: even minor rust can cause the walls of the barrel. This gradually wears away the syringe at the end of each day.
plunger to become stuck in the barrel. rust-resistant metal on the shaft's surface.
1. Rinse the syringe several times with a "dry"
• Rusting happens most rapidly when using water or
solvent, such as acetone.
solvents that may contain (or absorb) water.
2. Remove the syringe from the autosampler,
and wipe the plunger dry with a lint-free cloth.
3. Let syringe and plunger air dry.
"Ring around the neck" • Skin oils and other organic material. • Never touch the plunger shaft with your fingers.
(A dark ring between the top • Fine metal and glass particles from the syringe • If build-up appears when water is the solvent:
of the barrel and the end of plunger and barrel may be rubbing together. Once rinse syringe with acetone and wipe the plunger
the volume scale.) this happens, the plunger may bend if used further. clean at the end of each day.
Loose plungers • The syringe is nearing the end of its useful life. • Replace the syringe.
Accompanied by syringe leaks and • Note: Plungers normally feel "loose" when non-
area count reproducibility problems. polar solvents (like hexane and toluene) are used.
Needle tip position when withdrawing solvent 5 Tapered, fixed 23-26s/42/HP 5181-1273
Tapered, fixed 6/pk 23-26s/42/HP 5181-8810
Tapered, removable 23-26s/42/HP 5182-0835
Replacement needle for 5 µl syringe 3/pk 23-26s/42/HP 5182-0832
10 Tapered, fixed 23-26s/42/HP 5181-1267
Tapered, fixed 6/pk 23-26s/42/HP 5181-3360
Tapered, removable 23-26s/42/HP 5181-3321
Replacement needle for 10 µl syringe 3/pk 23-26s/42/HP 5181-3319
Tapered, fixed, PTFE-tipped plunger 23-26s/42/HP 5181-3354
Tapered, fixed, PTFE-tipped plunger 6/pk 23-26s/42/HP 5181-3361
Replacement plunger with PTFE tip 5181-3365
for fixed needle 10 µl syringe
Tapered, removable 23-26s/42/HP 5181-3356
Replacement plunger with PTFE tip 5181-3358
for removable needle 10 µl syringe
50 Tapered, fixed, PTFE-tipped plunger 23-26s/42/HP 5183-0314
100 Tapered, fixed, PTFE-tipped plunger 23-26s/42/HP 5183-2042
Tips & Tools
When cleaning syringes between
injections, use Agilent wash vials
(p/n 9301-0723) and diffusion
caps (p/n 07673-40180).
4 mL Clear screw top wash vials with screw caps (no septa) 144/pk 9301-0723
Septa for 4 mL vial 144/pk 9301-1031
Diffusion inserts for 4 mL vials 12/pk 07673-40180
4 mL wash vials with fill markings and caps 25/pk 5182-0551
Screw for mounting syringe 07673-20570
Quadrant tray (4 tray sections) 18596-40015
7673 Basic Supply Kit 07673-60840
Contains 10 µL syringes (6/ea), 23/26 gauge needles, 4 mL vials with
diffusion caps (144/pk), 2 mL automatic sampler vials with screw caps
(1,000/pk), GC septa (25/pk), vial racks (5/pk)
≤ 70 > 70 ≤ 70 > 70
samples/day samples/day samples/day samples/day
Replace sample 6 months 3 months 3 months Every month
probe
Steam clean 6 months 3 months 3 months Every month
Replace loop and With PM With PM With PM 6 months
deactivated tubing
Check tray tension 12 months 6 months 12 months 6 months
and alignment
Headspace Vials
Description Unit Part No.
Tubing
Tubing, solenoids to 6-port, deactivated 0410105017
Tube, probe to 6-port valve, deactivated 1300502506
Standards
OQ/PV Headspace Sample 5182-9733
Contains 0.2-0.3% t-butyl disulfide, 1,2-dichlorobenzene, and nitrobenzene in
ethanol
PM Kits
G1888A PM kit with 1 mL loop G1888-60702
G1888A PM kit with 3 mL loop G1888-60703
G1888A enhanced PM kit G1888-60704
CombiPAL and GC PAL CombiPAL and GC PAL Liquid Injection Vials and Caps
Liquid Injection Description Unit Part No.
Vials and Caps 2 mL vials
These micro and 2 mL vials and caps Crimp top vial, wide opening, clear 100/pk 5181-3375
are designed to work seamlessly with
CombiPAL and GC PAL magnetic needle Crimp top vial, wide opening, amber, write-on spot 100/pk 5181-3376
guides and bar code readers. Crimp top vial, wide opening, clear, write-on spot 1000/cs 5183-4492
Crimp top vial, wide opening, amber, write-on spot 1000/cs 5183-4493
Screw top vial, wide opening, clear 100/pk 5182-0714
Crimp/snap top vial, wide opening 100/pk 5182-0544
2 mL caps
Crimp cap, 11 mm magnetic 100/pk 5188-5386
Screw cap, PTFE/white silicone septa 100/pk 5182-0720
Snap cap, blue polyethylene, PTFE/silicone septa 100/pk 5182-0541
Micro vials
Crimp top vial, 0.8 mL, amber glass, flat bottom 1000/pk 5183-4487
Crimp top vial, 0.1 mL, clear, tapered 500/pk 5180-0844
Crimp top vial, 0.3 mL, clear, round 500/pk 5180-0841
Crimp top vial, 0.7 mL, amber, round 500/pk 5180-0805
Crimp top vial, 0.5 mL, amber, conical 500/pk 5180-0806
Micro caps
Crimp caps with PTFE/silicone septa 500/pk 5180-0842
CombiPAL Autosampler
CombiPAL
Headspace Supplies
Our fixed-needle headspace syringes
CTC syringe, G6500-80109
feature a sideport needle for gas flushing,
in conformance with strict CTC standards.
Use with Agilent’s Merlin Microseal to
minimize instrument downtime – and to CombiPAL Headspace Syringes
prevent lost or compromised data caused
Volume (µL) Description Gauge Part No.
by septum leaks and liner contamination.
1 Fixed needle 23 G6500-80107
Replacement plunger G4200-80101
2.5 Fixed needle 23 G6500-80109
Replacement plunger G4200-80107
5 Fixed needle 23 G6500-80111
Replacement plunger G4200-80108
CombiPAL Autosampler
You will also learn how to select the appropriate septa, liners, ferrules, and other
inlet supplies.
Long-Life Septa
• The preferred septum for autosamplers.
• Pre-pierced for extended life and reduced coring.
• Ideal for overnight runs.
• Up to 400 injections per septum.
• Plasma coating eliminates sticking.
• Maximum injection port temperature 350°C.
• Soft, 45 Durometer, easy on autosampler needles.
• Blister packaging for cleanliness and convenience.
Long-Life Septa
Description Unit Part No.
Septa Troubleshooting
Symptom Possible Causes Remedy
Baseline Change After Large Large leak at septum during Replace septum and use smaller
Peak injection and for a short time diameter needles.
thereafter (common with large
diameter needles)
Retention Times Prolonged Carrier gas leaks at septum or Check for leaks. Replace septum
column connection or tighten connections if
necessary.
Graphite (100%) 450°C • General purpose for • Easy to use stable seal. • Not for MS or oxygen
capillary columns. • Higher temperature limit. sensitive detectors.
• Suitable for FID and NPD. • Can be removed easily. • Soft, easily deformed
• Recommended for high or destroyed.
temperature and cool • Possible system contamination.
on-column applications.
Vespel/Graphite (85%/15%) 350°C • General purpose for • Mechanically robust. • Not reusable.
capillary columns. • Long lifetime. • Flows at elevated temperature.
• Recommended for MS and • Must retighten frequently.
oxygen sensitive detectors.
• Most reliable leak-free
connection.
Vespel (100%) 280°C • Isothermal operation. • Mechanically robust. • Leaks after temperature cycle.
• Can be reused or • Long lifetime. • Flows at elevated temperature.
removed easily. • Can be reused or • Must retighten frequently.
• Excellent sealing material removed easily.
when making metal or glass
connections.
SilTite (100% metal) N/A • Use with Capillary Flow • Provide leak-tight seals with • Not reusable.
Technology nut kits Ultimate Union, Deans Switch
and Effluent Splitter
Column Nuts
Description Part No.
Short Nuts
Universal column nut, 1/16 in. hex, 2/pk 5181-8830
Finger tight column nut for 530 µm columns* 5020-8293
Universal column nut, 5181-8830 Finger tight column nut for 320 µm columns and smaller* 5020-8292
Blanking plug, finger-tight style 5020-8294
6850 column nut, 2/pk 5183-4732
Extended column nut, VI inlet G3504-20504
High Temp SimDis PTV Inlet, 4 mm hex 5188-5312
Long Nuts
MS interface column nut, female 05988-20066
Column nut for long or long two-hole ferrules 05921-21170
Accessories
Open end wrench, 1/4 and 5/16 in. 8710-0510
*For use with graphite ferrules only
Split/Splitless Liners
Injection port liners have a variety of features to help vaporize the sample so that a true
representation of the sample enters the column. Additionally, Agilent liners are individually
packaged to maintain cleanliness until used. The part number and lot are silk screened
on the liner for quality control and user convenience, and lot tracking is available for
quality assurance.
Dimensions
Agilent liners are made to precise tolerances to ensure GC system accuracy and
reproducibility. Controlling the dimensions of the glass provides better consistency from
liner to liner, resulting in more reproducible results.
Length
Tight tolerances of liner length are needed to control internal volume and ensure proper
sealing between the septum and the inlet seal. Length can also be critical for more
repeatable positioning in the inlet relative to the inlet bottom since many analysts install
liners by measuring the distance from the O-ring to the top of the liner. Agilent has
designed liners with precise glass bumps on the bottom of the liner to automatically
position the liner in the inlet for greater reproducibility.
Glass Wool
• Less discrimination.
• Provides additional surface area for sample vaporization, increasing reproducibility.
• Serves as a trap for non-volatiles.
For split liners, Agilent specifies the placement of glass wool in the liner so that the
syringe penetrates the glass wool, wiping the syringe, to provide the most repeatable
results with Agilent autosampler and split/splitless inlet design thermal profile.
Even though it is deactivated, glass wool is considered the most active component
of a liner, increasing the possibility of adsportion and sample decomposition of
active compounds.
Liners with glass wool are not recommended for samples with active analytes – such as
phenols, amines, organic acids, pesticides and drugs of abuse – that could be irreversibly
adsorbed on surfaces in the inlet.
Deactivation
Agilent's proprietary deactivation is more resilient to degradation than other commercial
processes. With use, even deactivated liners become active. Replace the liner regularly.
Agilent recommends part number 5183-4647 as the top split liner choice for:
• Highest run-to-run area reproducibility
• Least discrimination for wide boiling point range samples
• Useable with widest range of conditions and sample types
• Easy self-adjusting installation
Helix Liners
Helix liners approximates the benefit of glass wool without the activity. The deactivated
glass spiral gives surface area without glass wool's active sites to vaporize and mix
sample before getting onto the column, and prevents sample from splashing onto
the bottom of liner and seal. Helix liners are recommended for slower injection speeds.
Helix Liners
Description Part No.
Helix liners
You can also improve the reproducibility and linearity of peak areas and avoid backflash
by matching:
• Inlet temperature
• Liner volume
• Injection volume
Decomposition
Loss of peak area or generation of new peaks, can sometimes be dramatically reduced by
changing liner type or by deactivating the liner and inlet with silanizing reagents.
Removing or reducing the amount of liner packing can also decrease inlet activity.
Column Troubleshooting
Inlet temperature Just above highest boiling point Ensures flash vaporization
of solutes (+20°C) Reduce if degradation occurs
Use higher for dirty samples and
higher-boiling solutes
Inlet liner Large volume > 0.8 mL Use with autoinjector
Small volume < 0.2 mL Use only for slow manual
injections and gas injections
Inlet packing None Use only with slow injection
Decreases degradation
Silanized glass wool Use for fast autoinjection and
dirty samples
Injection volume 0.5 - 2 µL liquid Depends on solvent, liner and
conditions
Injection technique Fast autoinjection Most reproducible
Hot-needle slow manual Less needle discrimination
Hot-needle fast manual Inject 1 - 2 µL/sec if narrow liner
is used and > 1 µL injection
Use for < 1 µL injections
Purge flow 20 - 50 mL/min Higher if using constant flow
Purge delay time 20 - 80 sec Adjust according to column flow
rate/liner type and sample
conditions
Oven temperature 10 - 25°C below solvent BP Necessary for solvent focusing
Column flow > 2 mL/min when possible Clears inlet fast
Reduces backflash and
decomposition
Septum purge 2 - 3 mL/min Reduces ghosting
Quantification Internal standard Maximizes reproducibility
External standard addition Use only with constant injection
volume
Retention gap 1 - 3 m, deactivated Reduces peak distortion
(1 - 2 m per µL injected) Promotes solvent and stationary
phase focusing
Available exclusively from Agilent, the Flip Top has a levered arm that attaches to any
6890/6850/5890 insert weldment and locks to the injection port using an adapter ring
screwed onto the inlet. Once installed, the user simply lifts the arm of the Flip Top which
releases the insert weldment from the injection port, and allows instant access to the liner.
The process is simply reversed to reseal the weldment to the port.
Insulation cup 2. Position the column so it extends 4 to 6 mm past the end of the ferrule.
Reducing nut 3. Slide the septum to place the nut and ferrule in the correct position.
Capillary column 4 to 6 mm 4. Insert the column in the inlet.
Ferrule (inside nut) 5. Slide the nut up the column to the inlet base and finger tighten the nut.
Inlet column nut 6. Adjust the column position so the septum is even with the bottom of the column nut.
7. Tighten the column nut an additional 1/4 to 1/2 turn. The column should not slide with
Septum a gentle tug.
8. Start carrier gas flow.
9. Verify flow by submerging the free end of the column in isopropanol. Look for bubbles.
Sample Considerations
Sample preparation is important for on-column injection because of:
• The potential for column overload, column contamination.
• The incompatibility of some solvents with the stationary phase.
• Dependence of the initial column temperature on the boiling point of the solvent.
Many of the problems associated with these variables can be resolved by using
a retention gap ahead of the analytical column.
Troubleshooting
Only columns with an immobilized stationary phase should be used with cool on-column
injection as this prevent displacements of the stationary phase by solvents. But problems
can still arise due to:
• Column overload.
• Solvent/stationary phase incompatibility.
• Column contamination.
Initial inlet temperature Equal to or 3°C above column Ensures sample focusing in
oven temperture solvent front
Initial inlet temperature ramp Same as oven (oven track) Simple and effective
Faster than oven Narrows initial peak width
Injection volume 0.1 - 2.0 µL liquid Use smaller injections for small
ID columns
Depends on column capacity
Injection technique Automatically slower injection Projects droplets away from
Fused silica needle syringe tip
Use for manual injection into
small ID columns
Tips & Tools Oven temperature Inlet temperature or slightly Prevents backflash
lower
There are some limitations to
cool on-column inlets, including Column flow 50 - 80 cm/sec Use for H2 carrier gas
the following: 30 - 50 cm/sec Use for He carrier gas
Septum purge 12 - 15 mL/min Use if installed to prevent
• Maximum sample volumes
ghosting
are smaller compared with other
inlets (0.5 µL to 2.0 µL). Quantification All methods Inherently reproducible technique
Lack of discrimination
• Solute peaks eluting just before
the solvent cannot be focused Retention gap requirements 1 - 3 m, deactivated Corrects peak distortion
and are difficult to determine. 530 µm Protects column from non-
volatile components
• Capilliary columns (especially those Permits autoinjection with
with a large phase ratio or small narrow-bore columns
inner diameter) can be easily
overloaded with sample.
• Parameters such as initial column
temperature, solvent nature,
and injection rate must often
be optimized.
Automatic Injection
1a Septum nut base for 320 mm assembly 19245-80521
1b Septum nut base for 530 mm assembly G1545-80520
1a
1b 1c
1d 2 Advanced Green Inlet Septa, 5 mm 50/pk 5183-4760
BTO Inlet Septa , 5 mm 50/pk 5183-4758
Manual Injection
2
3 1c Cooling tower assembly 19320-80625
4
Common Supplies
3 Spring 19245-60760
4 Inserts for capillary columns
For 200 µm columns, 1 ring 19245-20510
For 250 µm columns, 6 rings 19245-20515
5 For 320 µm columns, 5 rings 19245-20525
6
For 530 µm columns, no rings 19245-20580
Cool On-Column Inlet assembly
For 530 µm Al clad columns, 4 rings 19245-20780
5 320 µm, 0.5 mm ID graphite ferrule 5080-8853
6 Universal column nut 2/pk 5181-8830
Decomposition
Diagnose inlet sample decomposition by comparing retention times for decomposition
products to their standard retention times. Then try these options to improve results:
• Intracolumn direct injection.
• Deactivated glass liners.
• Lower inlet temperatures.
• Remove column packing in the inlet zone.
• Increase flow rates.
Flashback
Large sample injections can exceed liner capacity and flash back into the gas supply lines
and onto the septum. This can cause:
• Ghost peaks.
• Sample losses.
• Irreproducible peak areas.
• Decomposition.
Leaks
Septum and column leaks can cause column degradation and stationary phase
decompositions on flow-controlled column inlets.
• Change the septum on a regular basis and check column connections to help
eliminate leak holes.
• Keep the oven and inlet at room temperature when not in use or while changing
the septum.
Ferrule
Column nut
Nuts and Ferrules for 1/8 in. Packed Columns
1/8 in. stainless steel nut and ferrule set 20/pk 5080-8751
1/8 in. brass nut and ferrule set 20/pk 5080-8750
Vespel/graphite ferrule, 1/8 in. 10/pk 0100-1332
Top insert weldment
Flared end
Glass liner
Advantages
• No syringe-needle discrimination
• Minimal inlet discrimination
• Use of large injection volumes
• Removal of solvent and low boiling components
• Trapping of nonvolatile components in liner
• Split or splitless operation
• Retention time and area reproducibility approaching cool on-column injection
PTV inlets are actively cooled before and during injection by Peltier devices or by forced
gases (air, liquid N2, or liquid CO2). Cryogenic cooling of the inlet can reduce inlet
temperature enough to thermally focus gas injections from other sampling devices
in the liner. This is a distinct advantage of using PTV inlets in comparison to conventional
inlets for coupling auxiliary sampling devices to capillary columns.
Post-injection, PTV inlets are heated using electrical heaters or preheated compressed
air. Depending on design, inlet temperature ramps are either ballistic (i.e., ramped
to the maximum temperature at an uncontrolled maximum rate) or programmable.
Guide cap
Merlin cap Septum nut
PTFE ferrule
Merlin Microseal
Septum
Septumless head Kalrez seal
assembly
Valve body
Pressure spring
Septum head
Viton seal
Carrier gas tube Sealing element
Graphpak 3D ferrule
Liner
Silver seal
Flame Ignition
If the flame goes out or will not light:
• Measure the hydrogen/air and makeup flow rates – Low H2 or makeup flows indicated
a plugged jet, or a leak at the column fitting. Measure each gas flow independently.
• Confirm that the igniter is glowing during the FID ignition sequence.
• Check for partially or completely plugged jet – Formation of silica or carbon deposits
at the tip of the jet can cause plugging. Incorrect capillary column installation can also
FID collector assembly
cause plugging.
Detector fitting
Adapter
Gas Purity
For successful EC detection, it's important that the carrier and purge gases are very clean
and dry (99.9995% minimum purity). Moisture, oxygen, or other contaminants can result
in higher detector response but usually at the expense of both sensitivity and linear range.
Always precondition the column before connection to the detector.
ECD Warnings
Although beta particles at this energy level have little penetrating power – the surface layer of the skin or a few sheets
of paper will stop most of them – they may be hazardous if the isotope is ingested or inhaled. For this reason the cell
must be handled with care. Radioactive leak tests must be performed at the required intervals, the inlet and outlet
fittings must be capped when the detector is not in use, corrosive chemicals must not be introduced into the detector,
and the effluent from the detector must be vented outside the laboratory environment.
Filament Maintenance
The primary maintenance for a TCD involves the filament. Most procedures involve
improving filament life or keeping the filament from becoming damaged or contaminated.
To avoid filament damage and contamination:
Tips & Tools • Check for leaks.
After maintenance to the gas • Use gas purifiers to remove oxygen.
supply, inlet, or detector, check • Avoid chemically-active sample components, such as acids
for leaks with Agilent's Leak and halogenated compounds.
Detector (part number
• Turn off the filament when not in use.
G3388A). See page 18.
Cell Contamination
Cell contamination is a problem when a lower detector temperature is used to improve
sensitivity. If the cell becomes contaminated, a solvent flush of the detector may help to
remove the condensed material.
Solvent Flush
1. Cool the cell to room temperature and remove the column.
2. Place a septum in a nut or fitting assembly that fits onto the detector entrance
(7 mm septum in a 1/8 in. nut).
3. Place the nut or assembly on the detector fitting and tigthen. Verify the presence
of makeup gas flow.
4. Inject 20-100 µL volumes of toluene or benzene into the detector through the septum.
Inject a total volume of at least 1 mL of solvent. Do not inject halogenated solvents
such as methylene chloride and chloroform into the detector.
5. After the final injection, allow makeup gas to flow for 10 minutes or more. Slowly raise
the temperature of the cell to 20-30°C above the normal operating temperature.
6. After 30 minutes, decrease the temperature to the normal value and install the column
as usual.
Thermal Cleaning
The TCD can become contaminated with deposits from such things as column bleed
or dirty samples. A wandering baseline, increased noise level, or changes in response
on a checkout chromatogram all indicate contamination. Thermal cleaning, or bakeout
(heating the detector block to evaporate the contaminant), should be performed only after
you have confirmed that the carrier gas and the flow system components are leak free
and contaminant free.
Watch out for decreased sensitivity caused by samples that react with the filament,
originating from oxygen-contaminated carrier gas, leaks in plumbing, or column bleeding.
Samples with active components, such as acids and halogenated compounds can
chemically attack the filament as well. Also, sample condensation will contaminate
the detector cell if the temperature is too low.
Some types of contaminants can be removed by temperature bakeout.
Detector fitting
7890A Yes Standard TCD Analysis Filament Block Only Original G3432-67685
Gases/Hydrocarbons Must reuse heater/sensor
6890 No Standard TCD Analysis Filament Block Only Original G1532-60675
Gases/Hydrocarbons Must reuse heater/sensor
6890 No Standard TCD Analysis Filament Block Only Minifold G1532-60685
Gases/Hydrocarbons Must reuse heater/sensor
6890 Yes Recommended for Fatty Filament Block Only Original G1532-60690
Acid Analysis Must reuse heater/sensor
6890/6850 Yes Recommended for Fatty Filament Block Only Minifold G1532-60695
Acid Analysis Must reuse heater/sensor
6890/6850 No Complete Detector Assembly Minifold G2630-61230
Includes detector palette
and heater/sensor assembly
Standard design
Operation
The FPD uses three gases: air and hydrogen to support the flame, and nitrogen makeup
for capillary columns. The flow rates are critical for optimizing performance. Using
nitrogen as a makeup gas is essential to obtaining low MDLs. Do not use helium for the
makeup gas.
Gas purity
Sulfur contamination is a common problem and causes noise and/or a higher baseline
offset in the FPD. To minimize sulfur contamination and achieve the lowest MDLs,
use at least 99.9995% pure gases, clean tubing, and regulators with metal diagrams.
To protect your FPD over its lifetime, Agilent recommends gas generators or supply gas
filters designed to remove sulfur.
Contamination
The FPD is susceptible to build up of residue on the surfaces of the igniter coil, jet,
Glow plug
combustion chamber, and chamber window. The residue increases detector offset
and reduces the signal-to-noise ratio. The sample or column bleed usually cause the
residue. After a period of time, you may need to rebuild the detector and replace the
transfer line. Do not clean the transfer line, jet, or other parts with brushes or solvents.
To increase the time between servicing, remove the column, cap off the detector,
and run it at 250°C with the flame to bake off some of the residue. Replacing the igniter
may reduce baseline output. If these tactics are not effective, rebuild the detector.
If your solvent or sample is corrosive, it can erode the aluminum vent tube. Agilent
recommends using alternative stainless steel vent tubes for these applications.
Air Leaks
The original FPD design has three more internal seals than the new design. Temperature
For more information about gas cycling of the detector causes the ferrules to shrink and leaks to occur. The most common
purity and selection, including the leaks are around the fused silica transfer line. To eliminate these leaks, remove the
Renewable Gas Purification System, detector from the GC and tighten the transfer line fittings.
see pages 3-12. For both the original and new FPD, leaks can develop at the column nut or capillary
column adapter, the gang fitting at the EPC module, around the vent tube, or around
the igniter glow plug. If you are replacing fittings or O-rings, always use conditioned,
graphitized-vespel ferrules and Agilent's low sulfur O-rings. Make sure ferrules are
the correct size for your column.
• Column nut 5. Tighten the column nut until it grips the column. Tighten the nut an additional
1/8 to 1/4 turn with a pair of wrenches. Snug the septum against the base of
• Ferrule the column nut.
• Capillary column
6. Use a wafer cutter at 45° to score the column.
• Lint-free gloves
7. Snap off the column end. The column may protrude about 1 mm beyond the end of
the tool. Inspect the end with a magnifying loupe to make certain that there are no
burrs or jagged edges.
8. Remove the column, nut, and swaged ferrule from the tool.
9. Wipe the column walls with a tissue dampened with isopropanol to remove
fingerprints and dust.
10. Verify that a capillary adapter is installed in the detector fitting.
11. Carefully thread the swaged column up into the adapter. Finger-tighten the column
nut, then use a wrench to tighten an additional 1/8 turn.
If you are using a capillary column, the tip of the column must be at least 1 mm below the
surface of the jet. When you install the column, measure the distance from the sealing
surface of the ferrule to the tip of the column. This measurement is 153 mm for the
original FPD and 145 mm for the new FPD. For the new design, Agilent recommends
using the column measuring tool, part number 19256-80640.
Ferrule
1 Clamp 19256-00090
2 Screw, M3 x 25 (4 required) 0515-0683
3 Window O-ring, inner, 0.926 in. ID, orange 5061-5886
4 Convex lens 1000-1438
5 Lens housing 19256-20900
6 Flange ring 19256-00200
7 Fluorocarbon Elastomer O-ring, brown, 1.239 in. ID 5061-5890
Bead Life
To extend the life of the bead:
• Avoid polar stationary phase, if possible.
NPD bead • Use the lowest practical adjust offset or bead voltage.
• Run clean samples and keep the inlet/liner clean to minimize contamination.
• Turn off the bead when not in use.
• Keep the detector temperature high (320-335°C).
• Turn off the hydrogen flow during solvent peaks and between runs.
• If the NPD is off for an extended period of time in a high humidity environment, water
may accumulate in the detector. To evaporate this water, set the detector temperature
to 100°C and maintain it for 30 minutes. Then set the detector temperature to 150°C
and maintain it for another 30 minutes.
Gas Flow
The hydrogen, air and makeup gas flows should be measured frequently. They can drift
over time or be changed unintentionally without knowledge of it occurring. Each gas flow
should be measured independently to obtain the most accurate values. NPDs are very
sensitive to changes in the gas flows and consistent flows are necessary to maintain
performance levels.
Contaminants
Some chemical problems can also arise when using the NPD. Because it is a trace
detector, be careful not to contaminate the analytical system.
Glassware
Glassware must be very clean. Phosphate detergents should be avoided, so acid washing
of glassware followed by distilled water and solvent rinsing is recommended.
Solvents
Solvents should be checked for purity. Chlorinated solvents and silanizing reagents can
decrease the useful lifetime of the alkali source; excess reagent should be removed prior
to injection, if possible.
NPD Jets
Description Jet Tip ID Length (mm) Part No.
Detector fitting
Adapter
We will also show you how to execute key diagnostic tests and choose the right parts
and supplies.
Maintenance Schedule
Task Every week Every 6 months Every year As needed
The action required to remove contamination depends on the type and level of
contamination. Minor contamination by water or solvents can usually be removed
by allowing the system to pump (with a flow of clean carrier gas) overnight. Serious
contamination by rough pump oil, diffusion pump fluid or fingerprints is much more
difficult to remove and may require extensive cleaning.
Air Leaks
Air leaks are a problem for any instrument that requires a vacuum to operate. Leaks are
generally caused by vacuum seals that are damaged or not fastened correctly.
Leaks can occur in other places in the MSD, including the following:
• GC/MSD interface column nut
• Side/top plate O-ring (all the way around)
• Vent valve O-ring
• Calibration valve
• High vacuum gauge tube/controller fitting
• Cracked ion gauge tube (5973/5972/5971)
• Front and rear end plate O-rings
• GC/MSD interface O-ring (where the interface attaches to the vacuum manifold)
• Diffusion pump co-seal
• Baffle adapter O-ring
• Turbomolecular pump O-ring
• Vespel/Graphite ferrules, when heated
Remedy
• Check interface nut for tightness. Replace if necessary.
• Check and leak test the GC injection port.
Replacement Parts
MS interface column nut, 05988-20066
Description Part No.
Cleaning Solvents
It is common to see cleaning solvent peaks in the mass spectra shortly after the ion source
is cleaned.
Remedy
• Dry all cleaned metal parts in the GC oven before reassembling and reinstalling them.
Refer to specific cleaning procedures in your MSD Hardware Manual or MSD
The easiest way to insure that you Maintenance and Troubleshooting Manual.
minimize background contamination
• Use a temperature above the boiling point of the solvent but below the limit
and remove damaging oxygen
of the column.
from your carrier gas system is
to use a carrier gas purifying trap
right before the gas enters your Fingerprints
GC system.
Fingerprints contain hydrocarbons that can appear in mass spectra. Hydrocarbon
contamination is characterized by a series of mass peaks 14 m/z apart. The abundances
of these peaks decrease as peak mass increases. Fingerprint contamination is usually
caused by the failure to wear lint-free, nylon gloves during ion source cleaning,
GC inlet maintenance, or from installing the column. Use special care to avoid
recontamination of parts after you clean them. This typically occurs after some
maintenance or part replacement.
Remedy
Reclean using clean, nylon gloves and proper cleaning techniques.
Remedy
If m/z 446 appears, please call Agilent for assistance.
Remedy
Call Agilent for assistance.
A crude sign of a "leak-free" MS
system is when the ion ratio
of m/z 28 (nitrogen) over m/z 32
(oxygen) is approximately two
or greater.
Common Contaminants
Ions (m/z) Compound Possible Source
Sensitivity
Wrong retention time Check GC, method, application and carrier gas velocity.
Low signal Check GC, tune vacuum system.
Leaking injection port Clean the injection port.
Replace the injection port liner and septa.
Air leak Check and tighten interface nut, leak test GC
injection port.
Peak widths Do Autotune, check flow rate and temperature stability.
Interfering peaks Check time parameters, coeluting peaks, column type.
Excessive background Do Autotune and compare to background specifications.
Check time parameters.
Incorrect mass assignment Retune.
Abnormal spectra – excessive Check for contamination.
background contamination
Incorrect tuning Check tune file, retune, check sample.
Repeller voltage is too low Raise voltage to test for response.
Dirty ion source Clean source.
Repeatability
Dirty syringe needle Clean or replace the syringe.
Wrong syringe needle Replace syringe and septa.
Leaking injection port Perform injection port maintenance.
Replace the injection port liner, septa and liner O-ring.
Injection is too large Check method and injection volume, split ratio and/or
5975 MSD
splitless purge time.
Loose column connections Tighten column nuts on injection port or transfer line.
Replace column nuts and ferrule.
Variations in pressure, column flow Ensure the MSD is located in an environment where
and temperature the temperature is stable.
Keep MSD out of drafts and direct sunlight.
Check that the carrier gas is steady and well regulated.
Service the foreline pump and/or diffusion pump.
Dirty ion source Clean source.
Loose connections in the analyzer Check internal and external analyzer wiring conections,
make sure all are secure.
Ground loops Check main electrical lines.
Tools
Screwdriver, 3 in. Pozidriv shaft No. 1 pt, fits no. 2-4 screws 8710-0899
Screwdriver, 4 in. Pozidriv shaft No. 2 pt, Fits no. 5-10 screws 8710-0900
Open end wrench, 1/4 and 5/16 in. 8710-0510
MS Interface Column Installation Tool G1099-20030
Hex nut driver, 5.5 mm 8710-1220
Screwdriver, Torx T20 8710-1615
Ferrules
0.4 mm Vespel Graphite ferrule for 200/250 µm columns, 10/pk 5062-3508
0.5 mm Vespel Graphite ferrule for 320 µm columns, 10/pk 5062-3506
250 µm Vespel/Graphite ferrule, 10/pk 5181-3323
SilTite metal ferrules for 1/16 in. OD tubing, 10/pk 5184-3571
Includes 2 column nuts
SilTite Metal Ferrules, 1/16 in. x 0.4 mm ID, 10/pk 5184-3569
Includes 2 column nuts
SilTite Metal Ferrules, 1/16 in. x 0.5 mm ID, 10/pk 5184-3570
Vespel/Graphite ferrules, 5181-3323 Includes 2 column nuts
MS Interface Supplies
MS interface column nut, female 05988-20066
Column nut for long or long two-hole ferrules 05921-21170
Universal column nut, 2/pk 5181-8830
Preparing to Clean
Prior to cleaning, the mass spectrometer must be vented and the ion source must be
removed. Before venting the system, the following conditions must be met:
• Heated zones are less than 100°C.
• The diffusion pump is off and cool.
• The turbo pump is off and not spinning.
• The rough pump is off.
Always allow the automatic venting routine to run its full course. Improper venting may
cause diffusion pump fluid to be deposited into the analyzer (backstreaming). It can also
Electron Impact (EI) Ion Source
reduce the life of the multiplier or other sensitive MS parts.
The recommended cleaning material for the EI ion source is abrasive powder, aluminum
oxide powder.
Abrasively clean the surfaces that contact the sample or ion beam. Use an abrasive slurry
of alumina powder and reagent-grade methanol on a cotton swab. Use enough force to
remove all discolorations. Polishing the parts is not necessary; small scratches will not
harm performance. Also abrasively clean the discolorations where electrons from the
filaments enter the source body.
Warnings & Caution
5975/5973 MSD Electron Impact Ion Source Parts (EI)
Important: Do not abrasively or
ultrasonically clean the insulators. Item Description Part No. Inert
Part No.
Do not immerse filaments or lens
insulators in solvent. If insulators 1 Ion source body G1099-20130 G2589-20043
are dirty, clean them with a cotton 2 Drawout plate, 3 mm 05971-20134 G2589-20100
swab dampened with reagent-
3 Drawout cylinder G1072-20008 G1072-20008
grade methanol. If that does not
clean the insulators, replace them. 4 Lens insulator G3170-20530 G3170-20530
5 Ion focus lens 05971-20143 05971-20143
Take care to avoid contaminating
cleaned and dried parts. Put on 6 Entrance lens G3170-20126 G3170-20126
new, clean gloves before handling 7 Cap screw, gold plated G1999-20021 G1999-20021
the parts. Do not set the cleaned
parts on a dirty surface. Set them 8 High temperature filament G2590-60053 G2590-60053
only on clean, lint-free cloths. 9 Transfer line socket G1099-20136 G1099-20136
10 Repeller insulator G1099-20133 G1099-20133
11 Repeller G1099-20132 G2589-20044
6
9
5
4
10
3 11
2
1 7
8
5975/5973 MSD Electron Impact (EI) ion source assembly
6
11
5
4
3
2
1 9
8
10
7
Tips & Tools 6. Break 1 cm off the end of the column. Do not let any column fragments fall into the
analyzer chamber. They could damage the turbo pump.
The column installation procedure 7. Clean the outside of the free end of the column with a lint-free cloth moistened
for the 5975 MSDs is different with methanol.
from that for most previous MSDs.
Using the procedure from another 8. Adjust the column.
instrument may result in poor 5975 – Push the column through, and then let it pass the end of the Transferline by
sensitivity and possible damage 1-2 mm. With the analyzer door partially open, view through the glass plate to see
to the MSD. the column protrude.
5973 – Push the column through, and then let it pass the end of the Transferline by
1-2 mm as seen with the analyzer door open from that side.
5972 – Push the column in all the way and then pull it back about 1-2 mm.
Use the flashlight and magnifying glass if necessary to see the end of the column
inside the analyzer changer. Do not use your finger to feel for the column end.
9. Hand-tighten the nut. Make sure the position of the column does not change as you
tighten the nut. Reinstall the spring-loaded tip seal if it was removed earlier.
10. Check the GC oven to be sure that the column does not touch the oven walls.
11. Tighten the nut 1/4 to 1/2 turn. Check the tightness after one or two heat cycles.
Column
GC/MSD interface
(MSD end)
GC/MSD interface
1 to 2 mm (GC end)
GC
MSD
MSD Filaments
Description 5975 Series 5973 Series 5972 Series 5971 Series
Pressure Symptoms
5975/5973 Series
• Use the sight glass to determine the depth of the fluid. The recommended total fluid
charge is approximately 37 mL.
Foreline Pump
The oil in the foreline or rough pump should be replaced on average once every six
months, but can vary depending upon applications. After oil replacement, if a foreline trap
is present, the molecular sieves should be replaced.
Avoid contact with the pump oil. The residue from some samples may be toxic. Dispense
of used oil properly.
Pump Oils
Description 5975 Series 5973 Series 5972/5971 Series
MS standards
Calibration Standards
Description 5975 Series 5973 Series 5972 Series 5971 Series