Practical Steps in GC Troubleshooting - Agilent · Page 1 Practical Steps in GC Troubleshooting...
Transcript of Practical Steps in GC Troubleshooting - Agilent · Page 1 Practical Steps in GC Troubleshooting...
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Page 1
Practical Steps in GC
Troubleshooting Techniques, Tips, and Tricks
Mark SinnottApplication Engineer
GC Columns & Supplies
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“Everything was just fine and then this
happened!
How do I go about
TROUBLESHOOTING?”
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“Everything was just fine and then this
happened!”
Logic = Something changed (slowly or sudden) =
Something is different
Track Events – log book
-Changed column, liner, septum, syringe, etc.
-Injected samples, other method, etc.
-Did maintenance, cut column, inlet flush, etc.
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Troubleshooting Starts with Isolating the problem
•There are 5 basic areas from where the problem arises
•INJECTOR
•FLOW
•COLUMN
•DETECTOR
•ELECTRONICS
•But of course it can always be some COMBINATION
Knowing what can & can’t cause the symptom is the key
Logical Troubleshooting
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Typical Problems of Optimized Methods becoming
Unoptimized…and the Reason Why.
• Peak Tailing – Flow Path or Activity
• Bonus Peaks – In Sample or Back Flash (Carry Over)
• Split Peaks – Injector Problems, Mixed Solvent
• No Peaks – Wasn’t Introduced, Wasn’t Detected
• Response Changes – Activity, Injector Discrimination, Detector Problem
• Peak Fronting – Overload or Solubility Mismatch, Injector Problems
• Shifting Retention – Leaks, Column Aging, Contamination or Damage
• Loss of Resolution – Separation Decreasing, Peak Broadening
• Baseline Disturbances – Column Bleed, Contamination, Electronics
• Noisy or Spiking Baseline – Electronics or Contaminated Detector
• Quantitation Problems – Activity, Injector or Detector Problems
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Peak Tailing
INJECTOR or COLUMN is Active
-Reversible adsorption of active compounds
(-OH, -NH, -SH)
FLOW problem - dead volume, obstruction, poor installation, or severe column contamination
Miscellaneous - overloading of PLOT columns, co-elution, polarity mismatch between phase, solute or solvent, and some compounds always tail
*Tip = Inject a light hydrocarbon, should not tail unless flow path problem.
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Bonus Peaks
Column: DB-530 m x 0.53 mm I.D., 1.5 µm
J&W P/N: 125-5032
Oven: 60°C for 1 min
60-300°C at 20°/min
300°C for 3 min
Carrier Gas: Helium at 36 cm/sec
Injector: Split 1:100, 250°C
sample C7 - C20
Detector: FID, 250°C
1.00 2.00 3.00 4.00 5.00 6.00 7.00 8.00 9.00 10.00 11.00 12.00 13.00 14.00 15.00
Wh = 0.106
Wh = 0.029Wh = 0.030
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Bonus Peaks or Ghost Peaks
Contamination in INJECTOR, COLUMN or FLOW (carrier gas)
-Carry-over from a backflash or previous sample
-Bad tank of gas or traps have expired
-Septum bleed
*TIP = Run a blank run…it should be blank!
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Bonus ‘Siloxane’ Peaks
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GC Column Bleed Ions
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06000
7000
8000
9000
1.0e4
1.1e4
1.2e4
1.3e4
5 10 15 20 25Time (min.)
24 pA / 260°C
DB-624 30M x .53mm I.D., 3.0µm
12 pA / 320°C
DB-1 30m x .32mm I.D., .25µm
Column Bleed is Influenced by:
Phase type
Temperature
Column dimensions
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Split Peaks
INJECTOR (poor sample introduction)
-Injecting the sample twice (some how?)
-Mixed sample solvent (polarity difference)
-Sample in syringe needle (manual inject)
INJECTOR (activity)
-Breakdown (not really a split peak, 2 peaks)
-Sample degradation in injector
VOLATILITY
High boilers dropping out on Cold Spots
-Transfer line temps
-Unions or fittings not tracking column temp
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No Peaks
DETECTOR (not on or not operational)
INJECTOR (not working)
-Plugged syringe/plunger not moving
-Wrong injector (or detector)
-Huge leak (older systems)
-No carrier gas flow
NOT the COLUMN Unless…
-Broken column or No column
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Peak ResponseAll Change in Size
DETECTOR (response problem)
-Settings or flows changed
-Electronics failing
-Split ratio set incorrectly
-Wrong purge activation time
-Septum purge flow too high
-Injector temperature too low*
INJECTOR
-Leaky syringe
*Tip = Ask is it all of them or some of them, if all then injector or detector
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Peak ResponseSome Change in Size
INJECTOR or COLUMN is active/contaminated
-Irreversible adsorption of active compounds (-OH, -NH, -SH)
-Decomposition of sample
-Temperature Change – Discrimination
-Evaporation from sample
*Tip = If only some change, then ask which ones? If active compounds
then activity. If tracks volatility then cold spots or inlet discrimination.
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Peak FrontingShark Fin Shaped or Just Slight
COLUMN (contaminated)
-Overload (More pronounced with large solute and phase polarity differences)
INJECTOR
-Column installation
-Compound very soluble in injection solvent (need retention gap)
-Mixed sample solvent
OTHER
-Co-elution
-Breakdown
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Retention Time Shift
2.00
3.25
4.75
2.75
4.00
5.50
INJECTOR
-Leak in the septum
-Change in injection solvent
-Large change in sample concentration
FLOW
-Change in gas velocity
COLUMN
-Contamination
-Damaged stationary phase
-Loss of stationary phase
-Change in temperature
1.75
3.00
4.50
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min8 9 10 11
1400 ng
7 ng
Effect of Sample Overload on
Retention Time and Peak Shape
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Loss of Resolution
Resolution is a function of separation and peak width
Separation
Peak Width
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Loss of Resolution - Separation Decrease
COLUMN
-Different column temperature
-Contamination (more phase?)
-Matrix components co-eluting
-Different column phase?
Separation
Peak Width
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Loss of Resolution - Peak Broadening
FLOW
-Change in carrier gas velocity
-Make-up gas
COLUMN
-Contamination
-Phase degradation
INJECTOR (efficiency)
-Settings, Liner, Installation, etc.
Peak Width
Separation
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Baseline DisturbancesSudden Changes, Wandering, or Drifting
COLUMN or DETECTOR
-Not fully conditioned or stabilized (electronics)
-Contamination
FLOW
-Changes in carrier and/or detector gas flows
-Valves switching, leaks
WANDER
DRIFT
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Noisy Baseline
FLOW
-Contaminated gas
-Incorrect detector settings
COLUMN
-Bleed if at high temperature
-In detector flame (poor installation)
MILD
SEVERE
DETECTOR
-Air leak - ECD, TCD
-Electronics malfunction
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Spiking Baseline
DETECTOR
-Particles entering the detector
-Random: poor connection
-Regular: nearby "cycling" equipment (electronics)
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Quantitation Problems
DETECTOR
-Poor stability (electronics) or Baseline disturbances (contamination)
-Outside detector's linear range or wrong settings
Activity (adsorption) in INJECTOR or COLUMN
INJECTOR
-Technique, settings, conditions
-Syringe worn
OTHER
-Co-elution
-Matrix effects
-Sample evaporation – leaky vials
-Sample decomposition
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What is NOT caused by a Column???
Peaks!!
Any reproducible, sharp ‘chromatographed’ peak!
Siloxanes
Degradation product peaks: Endrin Aldehyde, Endrin Ketone,
DDE, DDD….
Carryover of sample compounds
Splitting of peaks
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Troubleshooting “Tools”
Bleed Profile: baseline problems
Inject a non-retained peak: peak shape problems
Test mix: all problems
Isolate the components: all problems
Condensation Test: baseline problems
Jumper Tube Test: baseline problems
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Generating a Bleed Profile
Time (min.)0 5 10 15 20 256000
7000
8000
9000
1.0e4
1.1e4
1.2e4
1.3e4
*DB-1 30m x .32mm I.D., .25µm
Temperature program // 40°C, hold 1 min // 20°/min to 320°C, hold 10 min.
Produce when the column is new (for future reference)
when there is a baseline problem
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Non-Retained Peak Shapes
Good Installation Improper Installation orInjector Leak
Potential problems:
Injector or septum leak
Too low of a split ratio
Liner problem(broken, leaking, misplaced)
Column position in injector and detector
Used to Check
Flowpath
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Test Conditions
Inlet: Split (250°C) Detector: FID (320°C)
Carrier Gas: Hydrogen Flow: 37.3 cm/sec (1.8 ml/min)
Holdup Compound: Methane (0.671-min)
Temperature Program: Isothermal at 110°C
Test MixUsed to determine how “good” the column is or if the problem
is related to the chemical properties of the analytes.
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Test Mixture Components
Compounds
Hydrocarbons
Alcohols
FAME’s, PAH’s
Acids
Bases
Purpose
Efficiency
Retention
Activity
Retention
Acidic Character
Basic Character
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Group/Prese
ntation Title
Agilent
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Own Test Mixture
• More specific to your application
• Selective detectors
• Concentrations specific to your application
• Use same instrument conditions
• Easiest to simply inject a calibration standard
• Store for future measure of column performance
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Isolate the Components
Simplify the system:
- example - Direct injection instead of P&T sample
introduction
Put in a known good column
Move column to a different GC, inlet or detector
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Condensation Test
Used* to isolate the cause of:
- Erratic baselines
- Ghost peaks or carryover
*Use when problems are worse after periods of GC non-use
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Condensation Test
Procedure
Leave GC at 40-50°C for > 8 hours
Blank run
Repeat a blank run immediately after the first blank run is
complete
Compare the two blank runs
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Condensation Test
Results
First blank run is worse:
- Contaminants (from injector, lines, traps or carrier gas) carried
into the column
Blank runs the same: contaminants are not strongly
focused on the front of the column
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Jumper Tube Test
Purpose
Helps to locate the source of contamination or noise
Isolates GC components
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Jumper Tube Test
Isolate the Detector
Remove column from the detector
Cap detector and turn on
Blank run
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Jumper Tube Test
Isolation of Detector - Results
Detector is the problem
Detector OK
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Jumper Tube Test
Isolate the Injector
Connect the injector and detector
- 1-2 meters deactivated fused silica tubing
Turn on carrier gas
Blank run
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Jumper Tube Test
Isolate the Injector - Results
Injector OK
Injector, lines or carrier
gas contaminated
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Jumper Tube Test
Isolate the Column
Reinstall the column
Setup as before
Blank Run
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Jumper Tube Test
Isolate the Column - Results
Problem returns: It’s the column
Problem gone: Previous leak, solid debris, or
installation problem
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And Now Let’s do Some
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Troubleshooting-Example #1
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A Real Troubleshooting Example
No Peaks
10 20 30 40 50
14
16
18
20
22
24
26
28
30
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Page 48
Is the flame Lit?
put glass piece over FID outlet----Answer in this case, Water condenses
look at output in instrument guage-- is the digital value greater than 0.0?
Answer in this case is approximately 16.2 pico amps
Is there flow through the column?
disconnect column from detector and measure flow with bubble solution or meter
Answer in this case was YES THERE IS FLOW
Assess the observations
Flame is lit and we have flow from end of column
Hypothesis: Sample not getting on column-syringe plugged?
Take syringe out and make injection manually on a dry paper towel
Answer – towel stayes dry (Syringe was clogged with septum)
Pull plunger out top, add solvent and replace plunger will usually dislodge septum particle
(should hear a little pop) If you can’t dislodge plug, Replace syringe
Reassemble the Injector & Re-inject
Logical Steps Taken to Find Peaks(most of our problems are leaks and plugs)
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Page 49
Peaks !!
0 10 20 30 40 50
14
16
18
20
22
24
26
28
30
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Page 50
Troubleshooting-Example #2
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Page 51
DB-624 COLUMNQC Test Mix
Column: DB-624
30m x 53mm I.D., 3.0µm
Carrier: Helium at 40 cm/sec
measured at 35°C
Injector: Mega Direct, 260°C
Detector: FID, 300°C
Oven: 35°C for 1.50 min
30°/min to 65° for 10 min
1. 1,2-Dichloropropane
2. Octane
3. Tetrachloroethylene
4. Chlorobenzene
5. Nonane
5 10 15 20 25
1.0e4
2.0e4
3.0e4
4.0e4
5.0e4
6.0e4
7.0e4
8.0e4
Time (min.)
2.71
7.43
10.92
12.49
17.42
20.78
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Page 52
Example of Column Contamination
DB-624 QC Test Mix*
After 75 Injections of Oily Sample
0 5 10 15 20
6000
7000
8000
9000
1.0e4
1.1e4
1.2e4
1.3e4
1.4e4
1.5e4
Time (min.)
2.21
3.30
6.03
9.26
10.4614.40
17.86
*Temperature program// 35°C hold 1.50 min // 30°/min to 65°C, hold 10 min
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Page 53
Column and Liner Contamination
Inlet coil of column
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Page 54
Example of Column Contamination
Removed 1 1/2 m from injector end *
Time (min.)0 5 10 15 20 25
5000
6000
7000
8000
9000
1.0e4
1.1e4
1.2e4 2.80
7.34
10.79
12.33
17.19
20.56
*Before Column rinse and bake
Temperature program // 35°C hold 1.50 min // 30°/min to 65°C, hold 10 min
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Page 55
Looks Fixed Doesn't it?
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Page 56
Example of Column Contamination
0 10 20 30 40 50 60 705000
6000
7000
8000
9000
1.0e4
1.1e4
1.2e4
1.3e4
Time (min.)
1 1/2 mtrs removed*
QC Test mix to Upper Temperature Limit
*Before Column rinse and bake.
Temperature program // 35°C, hold 1.50 min // 30°/min to 65°C,
hold 15 min // 20°/min to 260°, hold 50 min
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Page 57
Backflush Column
1/16" flexible teflon line to regulated pressure source
Beaker for solvent collection
Capillary column
Special connectorand ferrule
Flexible teflontubing
Special adapter
CapVial
Capillary column
Rinse with 10ml each:
Methanol, Methylene Chloride, Hexane
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Page 58
Jumper Tube Test
Used to Isolate Source of Contamination
. Cap off the detector and establish normal gas flows and temperature.
. Plot the baseline using a temperature program. If flat......
. Connect 1 meter of deactivated tubing between the injector and detector
. Plot the baseline using a temperature program. If flat.....
. Install the column.
. Plot the baseline using a temperature program.
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Page 59
Contaminated Inlet
Jumper Tube Test*
*1/2 mtr length of .53 mm I.D. deactivated tubing
Temperature program // 35°C, hold 1.50 min // 30°/min to 65°C for 15 min
0 10 20 30 405000
6000
7000
8000
9000
1.0e4
Time (min.)
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Page 60
Rinsing Injector
Carrier gas line
C6MeCl2
Injector body
GC Oven
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Page 61
Troubleshooting Tips
1. Isolate the problem.
(Blank Run, Inject Un-retained Compound, Jumper Tube Test)
2. Change only one variable at a time.
3. Compare before/after chromatograms.
(Peak shape, response, retention, baseline rise, background, look for trends, etc.)
4. Utilize Technical Support.
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Page 62
Remember
Multiple cause and effect
Do not change too many variables at once
Complete system = Carrier Gas + Injector +
Column + Detector + Data System
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Contact Agilent Chemistries and Supplies
Technical Support
1-800-227-9770 Option 3, Option 3:
Option 1 for GC/GCMS Columns and Supplies
Option 2 for LC/LCMS Columns and Supplies
Option 3 for Sample Preparation, Filtration and QuEChERS
Option 4 for Spectroscopy Supplies
Available in the USA 8-5 all time zones