GC Sampler 80/120 SPME Option User Manual
Contents
1. Needle bends during injection into sample vial or GC injection port Possible cause Remedy Improper manual sampling technique To prevent the needle from bending when doing manual SPME sampling 1 Adjust the SPME needle to the 0 2 depth gauge setting on the plunger first tickmark This will expose about 3 mm of the needle through the end of the black holder 2 Hold the SPME assembly on top of the sampling vial with the bottom of the black holder flush with the top of the vial cap 3 Hold the sampling vial and black SPME holder base securely with one hand Twist the stainless steel plunger clockwise with the other hand 4 Keep turning the plunger until the desired depth setting is achieved you will usually hear a pop when the needle pierces the septum 5 Expose the fiber and perform sample desorption as usual Improper manual desorption injection To prevent the needle from bending when doing manual SPME injections at technique 1 Adjust the SPME needle to the 0 2 depth gauge setting on the plunger first tick mark This will expose about 3 mm of the needle through the end of the black holder 2 Position the SPME assembly on top of the GC injection port or in the SPME inlet guide with the bottom of the black holder flush with the top of the injector or guide 3 Hold the black SPME holder base securely with one hand Twist the stainless steel plunger clockwise with the other hand 4 Keep turning the plunger unti2. 6 Sampling and injection depth of the Agilent SPME fiber can be controlled automatically 7 Conduct method development by using sequential methods withdifferentparameters ie incrementally increasing extraction times or extraction temperatures This manual covers the operation of the PAL Autosampler in the SPME mode with the basic software that is installed in the PAL Autosampler Ee Agilent Technologies 3 1 Introduction 6 User Manual Preparation Injector liner Injector Septum Agilent GC Sampler 80 120 SPME Option User Manual 2 Procedure for SPME Sampiling with the PAL AutoSampler Before beginning the analyst should optimize the chromatographic conditions for the analytes to be analyzed make sure an appropriate column temperature program and detector have been selected The injector liner is important in assuring good results when an SPME fiber is thermally desorbed Table 1 SPME GC inlet liners Description Part number Liner inlet for SPME deactivated 5188 6471 The SPME fiber assembly includes a septum piercing protective needle Figure 1 which is either a blunt or tapered hollow 23 gauge needle to protect the fiber coating during penetration of the septa oie Agilent Technologies t 2 Procedure for SPME Sampiling with the PAL AutoSampler Fiber Support Rod Protective Needle Fiber Figure 1 Detail of the fiber assembly In comparison liquid injection into a GC is u
3. Figure 5 Left injector unit with plunger holder installed Center unassembled kit components Right fiber holder and fiber assembly properly installed in the PAL Autosampler SPME adapter 6 Install a fiber assembly in the fiber holder and place it in the SPME adapter Figure 5 right Pull up the plunger so that the fiber is completely withdrawn into the protective needle 7 Place the SPME adapter partially into the injection unit In order to do this tilt the top of the SPME adapter foreword slightly Figure 6A and thread the protective needle carefully through the upper and lower needle guides at the bottom of the injection unit This process is made easier by 14 User Manual Procedure for SPME Sampiling with the PAL AutoSampler 2 lifting the magnet so it is level with the needle guide then push the needle through the opening Figure 6B 8 Push the plunger down so that approximately 1 5 to 2 cm of the fiber and fiber support rod are exposed 9 Place the plunger crosspiece into the plunger holder Allow the syringe adapter to click into place by magnetic force against the syringe carrier 10 Tighten the plunger retaining screw against the plunger crosspiece Figure 6C and press Continue A S iiic i Figure 6 Installing the fiber holder assembly NOTE Reverse the above procedure to remove the Agilent SPME fiber Be sure to pull up the plunger of the fiber holder so that the unprotecte
4. Technology Licenses The hardware and or software described in this document are furnished under a license and may be used or copied only in accordance with the terms of such license Restricted Rights Legend If software is for use in the performance of a U S Government prime contract or sub contract Software is delivered and licensed as Commercial computer soft ware as defined in DFAR 252 227 7014 June 1995 or as a commercial item as defined in FAR 2 101 a or as Restricted computer software as defined in FAR 52 227 19 June 1987 or any equivalent agency regulation or contract clause Use duplication or disclosure of Software is subject to Agilent Technologies standard commercial license terms and non DOD Departments and Agencies of the U S Government will receive no greater than Restricted Rights as defined in FAR 52 227 19 c 1 2 June 1987 U S Govern ment users will receive no greater than Limited Rights as defined in FAR 52 227 14 June 1987 or DFAR 252 227 7015 b 2 November 1995 as applicable in any technical data Safety Notices CAUTION A CAUTION notice denotes a hazard It calls attention to an oper ating procedure practice or the like that if not correctly performed or adhered to could result in damage to the product or loss of important data Do not proceed beyond a CAUTION notice until the indicated conditions are fully understood and met A WARNING notice
5. splitless conditions are consistent Use an automated SPME system to improve reproducibility 30 User Manual Troubleshooting 3 Reproducibility is poor Not using agitation during sampling or apply it Use a stir bar or soncication system to agitate the sample during inconsistently sampling Maintain consistent agitation conditions for all standards and samples Sample volumes are inconsistent Maintain consistent volumes for all standards and samples Sampling related t Desorption related Fiber discolored Possible cause Remedy Fiber is oxidized during fiber conditioning Minimize oxygen in carrier gas condition fibers in oxygen free gas flow orsample injection into GC i Reduce the injection port temperature to the recommended maximum setting Carbowax DVB coatings are especially sensitive to temperature lt 260 C is recommended t Does not usually affect the performance of the fiber Always minimize the oxygen content in the GC carrier gas to avoid oxidizing the fiber coating The polyacrylate coated fiber will discolor above 280 C Carbowax DVB may slightly darken during use however if the fiber turns brown lower the injection port temperature 265 C is the recommended maximum and check the system for leaks Heating during injection Sampling related t Desportion related Product related Number of injections from the fiber is less than previously obtained Possible cause
6. Solid samples not releasing analytes for extraction Competing analyte displaces compound of interest or interferes Not reproducing desorption conditions Remedy Time of extraction and temperature are the two most critical conditions to control Use a timing device and a calibrated thermometer to ensure reproducible results Remember that room temperature fluctuations will influence the ambient sample temperature Position fiber just below sample surface for immersion sampling and at a consistent position above the sample during headspace sampling Apply any pH or salt adjustments made to the samples uniformly across all extractions Determine minimum time for equilibrium using a standard mixture and controlled extraction conditions Note that full equilibrium is not required to be reached for all applications to achieve reproducible results Dilute samples to minimize solvent interference or use headspace sampling to minimize solvent effect Use internal standards surrogates or the standard addition technique to compensate for variations in sample matrix Minimize headspace volume to 50 or less and agitate the sample Maintain the same headspace volume and agitation conditions across all extractions Grind solid into small particles add to water and apply heat and agitation Reduce the extraction time to minimize displacement or interference Verify that the fiber position depth desorption time temperature and
7. Fiber will not retract or sticks in holder needle 29 Fiber breaks 29 Reproducibility is poor 30 Number of injections from the fiber is less than previously obtained 31 Fiber discolored 31 Fiber breaks in injector 32 Poor precision 32 Sample carryover 32 Extraneous peaks in blanks 32 This is a quick reference to symptoms and possible causes of the most common problems experienced by users oe Agilent Technologies 25 3 Normal Troubleshooting es Problem No peaks seen in GC analysis 26 Possible cause Instrument problems The splitter vent was left open The analyte concentration is too low to be detected Solvents present in sample competing with SPME extraction Headspace volume too large to establish equilibrium with fiber Coating on fiber deteriorated Incorrect SPME fiber used for extraction There is a leaking injection port septum or connection There is a leaking sample vial Loss during transport from the field Remedy Inject standard mixture detector response see GC troubleshooting guide for further assistance Run splitless injection for 2 minutes Start with known concentration 1 ppm of analyte in de ionized water mixture Optimize extraction by adjusting extraction time temperature and chemical condition of pH and salt Minimize solvents in the sample to lt 3 by dilution in water Reduce headspace to 50 or less agitate sample vigorously o
8. For direct immersion in liquid you want the entire fiber except the top 1 mm immersed in the liquid as shown in Figure 7 4 Adjust the vial penetration setting in the software until the fiber is in the proper position This may take several attempts The depth will remain the same in the agitator 5 For headspace ensure that the fiber is not touching the liquid and is centered in the headspace 6 Follow step 4 until the desired depth is obtained Using the SPME agitator heater The SPME Agitator can be used to heat samples and to agitate samples Either function can be used independently of the other The agitator can be used for 2 mL 10 mL and 20 mL vials Inserts are available to fit in the six agitator positions to handle 2 mL and 10 mL vials The agitator speed when using SPME is fixed at 250 rpm Faster speeds can be used during pre incubation but are not recommended during the fiber extraction process After the incubation temperature has been determined you can set the Standby temperature of the agitator This will keep the temperature constant during sampling 2 20 Procedure for SPME Sampiling with the PAL AutoSampler Menu gt Utilities gt Tray gt Agitator gt Standby Temp Parameters of agitator Incubation time 0 to 1440 minutes Agitator speed 250 760 rpm Speed for pre incubation speed set at 250 with fiber inserted Agitator on time 0 99 s The agitator rotates in intervals The ti
9. denotes a hazard It calls attention to an operating procedure practice or the like that if not correctly per formed or adhered to could result in personal injury or death Do not proceed beyond a WARNING notice until the indicated condi tions are fully understood and met Contents User Manual Introduction Procedure for SPME Sampiling with the PAL AutoSampler Troubleshooting Supplies References User Manual Agilent GC Sampler 80 120 SPME Option User Manual 1 Introduction Prior to reading this manual the reader should first read the Agilent GC Sampler 80 120 User Manual G6501 90000 and become familiar with the general operation of the PAL Autosampler including defining the position of objects and building methods and jobs The use of Solid Phase Micro Extraction SPME with the PAL Autosampler offers the analyst many features that will enhance the utility of this exciting sample preparation technique These include 1 Choice of 2 10 or 20 mL vials 2 Large number of samples Standard configuration is two trays with 98 2 mL vials per tray or 32 10 20 mL vials per tray Up to two additional trays can be added if necessary 3 Agitation and heating of the sample during the extraction Process 4 Controlled heating time for each sample 5 Each Agilent SPME fiber can be automatically pre conditioned before a series of runs or after the desorption step in each run with an optional heating accessory
10. plunger can be further extended to adjust the depth of the fiber in the vial When using a 2 cm fiber the vial penetration must be set at 31 mm to fully extend the fiber Vial penetration is usually set in the method If you do not have the software create an SPME Test method in the PAL controller Since it is not possible to see the fiber depth in the agitator set the fiber depth out of the tray Use the same depth when the vial is in the agitator Prior to setting the injection penetration the sample volume User Manual User Manual Procedure for SPME Sampiling with the PAL AutoSampler 2 must be determined especially for direct immersion into a liquid See Table 1 for recommended volumes Table 3 Recommended volume sample for various vial volumes and fiber length Headspace sampling Direct Direct 1 cm fiber Headspace immersion in immersion in Vial volume length 2cmfiber liquid 1 cm liquid 2 cm 2 mL 0 4 0 6 mL NR 1 2 1 3 mL NR 10 mL 4 0 6 0 mL NR 9 0 mL NR 20 mL 10 15 mL 10 13 mL 18 mL 18 19 mL 1 Place the vial filled to desired liquid volume in the 8th position of the 32 vial tray 14 position of 98 vial tray Be sure that for 32 vial tray that the PAL has been set for the proper Traytype vial size 2 Using the Agilent FSE Driver Run SPME out of Tray method select the proper tray and vial position You may want to increase your extraction time to 1 min or more 3 Check the fiber depth in the sample
11. Agilent GC Sampler 80 120 SPME Option User Manual ope Agilent Technologies Notices Agilent Technologies Inc 2011 No part of this manual may be reproduced in any form or by any means including electronic storage and retrieval or transla tion into a foreign language without prior agreement and written consent from Agilent Technologies Inc as governed by United States and international copyright laws Manual Part Number 66504 90010 Edition First edition October 2011 Printed in USA Agilent Technologies Inc 5301 Stevens Creek Boulevard Santa Clara CA 95051 USA Warranty The material contained in this docu ment is provided as is and is sub ject to being changed without notice in future editions Further to the max imum extent permitted by applicable law Agilent disclaims all warranties either express or implied with regard to this manual and any information contained herein including but not limited to the implied warranties of merchantability and fitness for a par ticular purpose Agilent shall not be liable for errors or for incidental or consequential damages in connection with the furnishing use or perfor mance of this document or of any information contained herein Should Agilent and the user have a separate written agreement with warranty terms covering the material in this document that conflict with these terms the warranty terms in the sep arate agreement shall control
12. PAL AutoSampler 2 analytes off the fiber and may drive more water into the fiber and needle sheath After the optimum temperature is obtained select an appropriate extraction time Keep in mind the total GC cycle time when setting extraction times Optional bakeout of the fiber after injection With some fibers a high temperature is necessary to desorb the analytes completely Often the GC injector cannot be set to a high enough temperature because a column with a low temperature limit is installed With the PAL Autosampler the user can bake the fiber after desorption in a separate bakeout station Figure 8 This is an optional piece of hardware ta Figure 8 Optional bakeout station The baking occurs with a flow of inert purge gas To enable this feature install the bakeout station Then define the position of the bakeout station NdlHeater as follows Menu gt Utilities gt Injector gt NdlHeatr Set the x y z parameters The path is mixed up Temperature XYZ positions are reversed The temperature can be set in increments of 5 C from 30 C to 350 C To set the temperature Press Menu gt Setup gt Objects gt Injector gt NdlHeatr 21 2 Procedure for SPME Sampiling with the PAL AutoSampler Building an SPME method See the Agilent GC Sampler 80 120 User Manual for details on how to build a method The parameters in the SPME method are discussed in Table 4 Table 4 Parameters in the SPME m
13. Remedy Fiber is oxidized during fiber conditioning or Minimize oxygen in carrier gas condition fibers in oxygen free gas sample injection into GC t flow Reduce injection port temperature to the recommended fiber maximum Coating on fiber deteriorated Replace fiber Fibers are reusable and will last for 50 injections on average Fiber was exposed to solvents that cause swelling Do not expose PDMS coated fibers to nonpolar solvents such as of coating pentane methylene chloride or diethyl ether Do not expose Carbowax fibers to polar solvents Sampling related t Desorption related Product related User Manual 31 3 Troubleshooting Fiber breaks in injector Possible cause Improper depth in injector Septum corings or other particles are in the injector Remedy Verify see above that the bottom of the SPME fiber syringe is not less than 5 mm into the insert Replace insert If septum particles are present consider using a seal such as the Merlin Microseal to eliminate the septum Poor precision Possible cause Vials are leaking Poor sample handling Remedy Verify that the cap cannot be turned after sealing Reduce the extraction temperature to see if the precision improves Temperatures gt 80 C are not recommended See the Advantage Note on SPME method development in the SPME Application and Advantage Note section of this manual Sample carryover Possible cau
14. d fiber is not pulled through the upper and lower needle guides User Manual 15 2 16 Procedure for SPME Sampiling with the PAL AutoSampler Standby position of the fiber In this step the end of the fiber is set so that it is just barely withdrawn into the protective needle This will minimize coring when penetrating vial or injector septa From the Job Queue page enter the following sequence Menu gt Utilities gt Syringe Scroll through the various parameters until you reach Standby Pos and press Enter With your thumb push up the lower needle guides until the end of the protective needle is visible If the fiber is not exposed turn the dial counterclockwise until you can see the fiber Then turn the dial clockwise slowly until the end of the fiber is flush with the end of the hollow tube Turn the dial clockwise an additional 0 5 mm Enter the value and press F4 Home Repeat this procedure whenever a fiber is installed Checking alignment of PAL Autosampler in the injectors The PAL should have been initially aligned with the injection port during setup This is accomplished without a needle in the injector The needle guide is used to position the unit For SPME the needle alignment is very critical 1 Place the SPME adapter container holder and assembly into the PAL injector 2 Follow the sequence in PAL menu setup injectors 3 Select the appropriate injector and continue 4 The needle will puncture th
15. e injection port septum nut opening 5 Using x y z positions align the PAL injector so the needle is straight in the x and y positions This may require a very slight alignment but it will assure that the needle will properly hit the center of the septum nut opening Setting fiber position in the injection port The fiber position in the injection port is controlled by two parameters The first parameter is the needle penetration depth This is fixed for SPME at 33 mm The second parameter that controls the fiber position is the Injection Penetration After you have set the injection position and made an injection with a fiber installed verify that the fiber is intact after the injection Press F1 Menu and then F1 Change Syr to view the fiber User Manual Procedure for SPME Sampiling with the PAL AutoSampler 2 Injection penetration Range 44 67 mm Injection Penetration is the distance that the fiber is pushed into the injection port with the plunger The default setting is 54 mm and this appears to be suitable for nearly all standard GC injection ports The hot zones can vary between injection ports so fine tuning the distance can be obtained if desired The key is to use the same depth for all of the analyses to insure consistency 1 Remove the septum nut loosen the injection port liner lock and remove the liner Place the liner against the septum contained inside the septum nut Mark the position on the li
16. e nut slightly to allow for improved injection Use pre drilled injection port septa or a septumless injector system for example Merlin Microseal Do not expose PDMS coated fibers to nonpolar solvents such as pentane methylene chloride or diethyl ether Do not expose Carbowax fibers to polar solvents Loosen the top screw on the holder assembly slightly to allow for free movement of the plunger Desorption related t Sampling related Product related Fiber breaks Possible cause Fiber was not retracted into the protective needle after removal from sample vial or injection port t The end of the needle is plugged with a piece of septum Remedy Retract fiber into protective needle during insertion into vial injection port and removal Injection port septum nut is overtightened Loosen the nut slightly to allow for improved injection Use pre drilled injetion port septa or a septumless injector system for exampleMerlin Microseal Sampling related t Desorption related User Manual 29 3 Troubleshooting Normal Problem Reproducibility is poor Possible cause Time and temperature variations during sampling Not consistently positioning the fiber at the same depth during sampling pH or salt conditions varying during sampling Equilibrium is not reached during extraction Varying organic content in the samples Varying headspace in sample vials during headspace extraction
17. efer to page 33 Special adapters are required for the agitator when using 10 mL and 2 mL vials The adapters for the 10 mL vials are shipped with the instrument The 2 mL vial adapters are available as an option Selecting the appropriate fiber assembly The appropriate SPME fiber for your analysis is based primarily upon three criteria 1 Molecular weight size and shape of the analyte s 2 Analyte polarity 3 Concentration range of analytes in sample User Manual User Manual Procedure for SPME Sampiling with the PAL AutoSampler 2 The data in Figure 3 provides general guidance on selection of fiber coating type based on the molecular weight range of the target analytes TPR 7pm PDMS 30m POMS ren 100pm Poms SSS SSeS LL DVB DVB Carboxen C tbexen 0 150 300 450 Analyte Molecular Weight Range Figure 3 Fiber coating type based on molecular weight range 7 um Polydimethylsiloxane PDMS Absorbent Nonpolar 30 um PDMS Absorbent Nonpolar 100 um PDMS Absorbent Nonpolar 85 um Polyacrylate PA Absorbent Polar 65 um PDMS DVB StableFlex Adsorbent Bipolar 55 um 30 um DVB Carboxen PDMS SF Adsorbent Bipolar 85 um Carboxen PDMS StableFlex Adsorbent Bipolar Polar analytes are best extracted by polar fibers Adsorbents are better for trace level of analytes with a more narrow linear range whereas absorbents are better for higher concentration levels and broader concentra
18. ethod Parameter Value Comments Cycle SPME Syringe Fiber Pre Inc time 00 00 00 23 59 59 Allows the sample to be preheated prior to insertion of the fiber Incubat temp 30 0 C 200 Cor OFF for Sampling out of the Tray OFF at ambient temperature without agitation A maximum of 80 C is suggested Agi On time 0s 99s Set Os to turn off agitation Used for Sampling out of Tray Agi Off time 0s 99s Vial Penetr 22 0 31 0 mm Distance from top of vial septum to end of fiber Figure 7 Extract time 00 00 10 23 59 59 Sampling time in liquid or headspace Desorb to None Waste 2 Normally an injector such as GC Inj1 GC Inj2 or Front or Rear is entered here Inj Penetr 44 0 mm 67 0 mm Distance from top of injector nut to end of fiber Desorb time 00 00 10 23 59 59 Time in injector Fiber bakeout GC runtime 00 00 00 23 59 59 00 00 30 23 59 59 For baking out the fiber after desorption in the optional bakeout station If 0 the unit does not move to the bakeout station Enter the complete GC cycle time including cool down and re equilibration to coordinate the PAL Autosampler and GC cycles User Manual Procedure for SPME Sampiling with the PAL AutoSampler 2 After the incubation temperature is determined it is convenient to set the standby temperature of the agitator to this temperature Enter the following sequence from the Job Queue page Menu gt Utilities gt Tray gt Ag
19. itator Scroll down to Standby Temp and set the temperature Running the SPME test sample The SPME Sensitivity Test Sample is composed of 1 mL each of nitrobenzene and nitrotoluene in water 1 methanol has been added to stabilize the sample These compounds were selected because they exhibit a good response with many GC detectors including the flame ionization detector electron capture detector thermionic selective detector and the ion trap detector A representative SPME test sample chromatogram is shown in Figure 9 Sample SPME Evaluation test mix SPME fiber 100 um PDMS Fiber Extraction 10 min immersion in 4 mL vial ambient no agitation Desorption 2 min at 240 C Column 15 m x 0 25 mm x 1 0 um Oven 60 C 1min to 200 C at 20 C min Detector FID Carrier gas helium 40 cm sec at 60 C constant pressure Injection 240 C splitless split closed inital 0 5 min then vented at 50 mL min 1 Nitobenz re 2 Nitotoluere m ms Em g ay Ai mmm so sm a a see Zu ER a En se oe mmm u 0 2 4 6 8 10 12 14 Figure9 Chromatogram of the SPME test sample User Manual 23 2 Procedure for SPME Sampiling with the PAL AutoSampler 24 User Manual Agilent GC Sampler 80 120 SPME Option User Manual 3 Troubleshooting No peaks seen in GC analysis 26 Extraneous peaks in analysis 27 Needle bends during injection into sample vial or GC injection port 28 Needle bends with automated injection system 29
20. l the desired depth setting is achieved you will usually hear a pop when the needle pierces the septum 5 Expose the fiber and perform sample desorption as usual Vial or injection port septum is too tight l Slightly loosen the vial closure or injection port nut Septa in sample vial injection port is too Use LB 2 septa for injection port or silicone septa with lt 10 mil Teflon on thick or coated with thick Teflon coating i sampling vials Shorten the amount of exposed needle on SPME holder to 0 5 inch or 1 cm before puncturing the vial septa Adjust the holder needle setting to the desired depth for sampling Do not use butyl rubber style septa Sampling related t Desorption related 28 User Manual Needle bends with automated injection system Troubleshooting 3 Possible cause GC inlet liner is too narrow or packed with adsorbent material Needle is out of alignment with injection port or sample vial Remedy Use larger splitless inlet liners 0 75 mm id or larger without glass wool or adsorbents Reference autoinjector manual on alignment Desorption related t Sampling related Fiber will not retract or sticks in holder needle Possible cause The end of the needle is plugged with a piece of septum The fiber was exposed to solvents that caused swelling of coating The top screw in the holder assembly is too tight Remedy Injection port septum nut is overtightened Loosen th
21. leaves the injector to verify the integrity of the seal A subtle leak will be indicated by shifts in retention time no peaks or poor area count precision or the presence of air in a mass spectrometer Injector temperature Although temperature programmable injectors have become popular for minimizing decomposition of labile compounds and for eliminating discrimination based on volatility SPME fibers are generally desorbed under hot isothermal conditions Rapid desorption from the fiber is necessary for sharp peaks without sample carryover Injector temperature is normally 10 20 C below the temperature limit of the fiber and or the GC column Typical inlet temperatures range from 220 C to 310 C 2 10 Procedure for SPME Sampiling with the PAL AutoSampler Sample vials Temperature programming causes peak broadening The thermal desorption shall happen within milli seconds Many SPME applications will require the heating of the sample For these applications only vials recommended for the PAL Autosampler should be used These vials are 10 mL and 20 mL with magnetic crimp top caps and an 8 mm opening and capped with 1 3 1 5 mm thick septa Do not use vials with a butyl rubber septa Two mL vials with magnetic caps are also available however these are not recommended as the holes in the caps are small and fiber breakage is possible For a complete list of vials caps and septa recommended for optimum SPME performance please r
22. me that the agitator rotates in one direction is time on During extraction with SPME fiber the agitation is only in one direction and is on the entire time Agitator off time 0 99 s This is the amount of time that the agitation is off between intervals For direct immersion of liquid samples If direct immersion is required to extract analytes of interest an agitator can be used to shorten the extraction process Usually heat is not used when direct immersion is being used However you may want to set the agitator temperature to 30 C to keep consistency between samples For analytes with low volatility some analysts will heat the sample to shorten the extraction time For headspace sampling of liquids or solids If samples have sufficient volatility headspace sampling is usually a better choice than immersion Samples extract more rapidly in headspace the fiber remains clean and usually less interfering peaks are observed For most samples heat will be applied For liquid samples agitation may be used along with heating For solid samples agitation may not be necessary with heating of the sample Optimize heating and time by designing multiple methods First select a fixed time and vary temperature Typical temperature range is 35 C to 70 C Rarely is the extraction temperature set above 70 C because the increased temperature will desorb User Manual User Manual Procedure for SPME Sampiling with the
23. ner that is the hot zone range The manufacturer should report this distance from the top of the liner From the top of the hot zone range measure 1 cm down into the liner This is the point where you want the tip of the fiber to be placed Note that this is the bottom of the fiber so 1 cm above the tip should be in the hot zone of the injection port Measure the distance in mm from the top of the nut to the point where you want the tip of the fiber to be in the injection port This distance is the injection penetration distance Set this distance in the method and the fiber should be desorbing in the hot zone of the injection port For 2 cm fibers increase the injection penetration depth to the maximum value to fully expose the fiber User Manual 2 18 Procedure for SPME Sampiling with the PAL AutoSampler Setting fiber depth in the sampling vial Vial penetration The main parameter for controlling the depth into the vial is vial penetration Vial penetration is the distance the plunger moves after the needle pierces the vial The distance that the needle pierces a vial is fixed at 11 mm Protective Needle Seal Fr 1 Magnetic Steelcap Fiber Support Rod SPME Fiber i Vial Penetr 22 0 mm 31 0 mm Figure 7 Showing the Vial penetr parameter Range 22 31 mm Vial penetration determines how far the fiber extends into the vial At 22 mm a 1 cm fiber is fully exposed however the
24. r increase the sampling temperature Replace fiber Fibers are reusable and will last for 50 injections on average This is beyond the scope of this guide Please contact technical service 800 359 3041 for assistance if you are experiencing problems selecting the appropriate fiber for your application Replace septum and tighten nut properly Replace vial septum and seal cap properly Move the depth adjusting lever of the portable field sampler to the top most locking slot so the end of the septum piercing needle is totally withdrawn into the sealing septum of the sampler If the fiber will be stored for more than one day we recommend that it be stored at subambient temperature This reduces the chance of breakdown and loss of sample that could occur at higher temperatures Analysis related t Desorption related Sampling related Product related User Manual Normal Problem Extraneous peaks in analysis Troubleshooting 3 Possible cause Septa used in sampling vial or injection port is outgassing organic contaminants i Fiber is not preconditioned prior to sampling Inlet liner is contaminated or contains septa particles GC column is collecting analytes on the front of the column because it is not heated high enough in sample analysis Interfering peaks coelute with analytes of interest Carryover from previous analysis of the fiber Cross contamination from laboratory air Cross contamina
25. rExp position From the Job Queue page enter the following sequence Menu gt Setup gt Objects gt Vials gt FiberExp Assuming the agitator is installed on the right side set the x y and z parameters so that the right edge of the injection unit is resting on the left rear edge of the agitator Figure 4 If the agitator is on the left side then the left edge of the injector unit should rest on the right rear edge of the agitator Press F4 Home Do not position the round screw head from the needle guide directly on the edge of the agitator lid With the side play of the lid the needle guide could slip away 12 User Manual Procedure for SPME Sampiling with the PAL AutoSampler 2 Figure 4 Injection unit in the FiberExp position with the right edge just touching the left rear edge of the agitator Installation of the SPME adapter 1 Press F1 Menu and then F1 Chang Syr The injection unit will move to a position that will facilitate installation of the SPME adapter 2 Ifthe injection unit is directly over a sample tray move the Chang Syr position 3 Press Continue and then Utilities gt Syringe 4 Press F3 Set Pos and set the x y z positions to a location where there is a clear space under the fiber Press F4 Home and repeat Step 1 User Manual 13 2 Procedure for SPME Sampiling with the PAL AutoSampler 5 Install the plunger holder into the injection unit Figure 5 left ID 24 Fiber 10mm Scale 36mm
26. s 35 5 References 36 User Manual Apg Agilent Technologies Agilent Technologies Inc Printed in USA October 2011 G6504 90010
27. se Fiber is not fully desorbed Fiber support rod is submerged in liquid sample Remedy Increase desorption time and or temperature or bake out the fiber after each injection Reduce the fiber penetration depth in vial or reduce the amount of sample in the vial Extraneous peaks in blanks Possible cause Contamination is in the GC Contamination is in the sample vial septa Fiber bends in Agitator Remedy Verify that the GC is clean by making a run without injecting a sample Sample an empty vial without a septum installed Sample an empty vial with a septum installed If the contamination is from the septum bake the septum in a laboratory oven at 150 C overnight This will minimize extraneous peaks Vial is not completely released from the needle when the injection unit moves away Replace short tension cord PM Belt from Agitator is worn out or even broken Replace belt O Ring from Agitator PM 32 User Manual User Manual ege a Supplies Agilent GC Sampler 80 120 SPME Option Sampling vials for PAL Autosampler Headspace Table 5 Based on studies involving Agilent SPME fiber durability with the PAL Autosampler system it is important that thinner septa be used to seal vials for SPME use We recommend a 1 5 mm silicone PTFE lined septa with SPME neck vials or screw cap vials A steel cap should be used with screw top vials and either aluminum tin or steel can be used wi
28. sually accomplished with a tapered 26 gauge needle Therefore sample introduction with a SPME fiber is more likely to result in septum failure A septum less injector seal such as the Merlin MicrosealTM Figure 2 is highly recommended Figure 2 The Merlin Microseal can be istalled in a GC injector in place of a septum The device contains a duckbill that allows a needle to enter the injector without leaking The higher the gauge number the narrower the outer diameter User Manual User Manual Procedure for SPME Sampiling with the PAL AutoSampler 2 Table 2 Merlin Microseal Description Part number High pressure Merlin Microseal starter kit 5182 3442 Includes microseal septum and nut Microseal high pressure septum 5182 3444 Microseal high pressure nut 5182 3445 It is possible to use a conventional GC septum with SPME To minimize septum failure the following procedure is recommended 1 Install a new septum Pre pierce the septum with a syringe needle first 2 Puncture the septum with a SPME protective needle three or four times 3 Remove and inspect the new septum Pull off and discard any loose particles of septum material 4 Reinstall the septum 5 Metal fiber assemblies with 23 gauge needles will core septa more rapidly 6 Check inlet liners for particles replace liner if particles are present The user should monitor the head pressure on the column as the protective needle enters and
29. th the SPME neck vial A 1 mm thick Viton septa works best with screw cap vials For SPME use we strongly recommend that caps with a 8 mm hole be used instead of the 5 mm hole Sampling vials Description Quantity Catalog number Crimp vial 2 mL clear wide opening 100 5181 3375 Crimp vial 11 mm magnetic silicone PTFE septa 100 5188 5386 Crimp vial amber glass 0 7 mL 1000 5183 4487 Crimp cap 8 mm silicone PTFE 500 5180 0842 Screw top vials 2mL clear wide opening 100 5182 0714 Blue screw caps PTFE silicone septa 100 5182 0720 Snap top vial 2 mL clear wide opening 100 5182 0544 Blue snap cap PFTE silicone septa 100 5182 0541 woe ete je aan eee Agilent Technologies 33 4 Supplies 34 User Manual Useful web pages Books Trademarks Agilent GC Sampler 80 120 SPME Option User Manual 5 References e www agilent com chem e University of Waterloo SPME research http spme uwaterloo ca e University of Texas SPME bibliography http www cm utexas edu brodbelt spme_refs html 1 J Pawliszyn Solid Phase Microextraction Theory and Practice Wiley VCH Inc New York 1997 2 S Wercinski editor Solid Phase Microextraction a Practical Guide Marcel Dekker New York 1999 CarbowaxUnion Carbide Chemicals amp Plastics Technologies Corp Carboxen StableFlex Thermogreen Sigma Aldrich Co Microseal Merlin Instrument Company Viton E l duPont Nemours amp Co Inc ois Agilent Technologie
30. tion during transport from the field Remedy Prebake the vial septa for 2 hours at 68 C prior to use Use low bleed LB 2 septa to minimize injection port septum bleed Precondition fiber at the recommended conditioning temperature in the fiber instruction sheet Once fiber is preconditioned only 1 2 minutes is required to clean the fiber prior to sampling Replace the inlet liner Use pre drilled septum or a septumless injector system e g Merlin Microseal Complete GC analysis temperature program before injecting another SPME extract and keep column at 150 C when not in use Change GC column or temperature program Bake out fiber at the recommended conditions for several additional minutes Do not expose the fiber to the laboratory environment at any time during the sampling or injection steps Analyze control blanks using the same handling process as the sample to determine if technique or laboratory cross contamination is present Move the depth adjusting lever of the portable field sampler to the top most locking slot so the end of the septum piercing needle is totally withdrawn into the sealing septum of the sampler If the fiber will be stored for more than one day we recommend that it be stored at subambient temperature This reduces the chance of sample cross contamination Sampling related t Analysis related Product related Desorption related User Manual 27 3 Troubleshooting Lu
31. tion level ranges Installing a fiber assembly into the SPME holder When using the PAL Autosampler we highly recommend the use of metal superelastic assemblies The second best choice are assemblies with 23 gauge needles The wall of the 23 gauge needles is thicker and less likely to bend when piercing septa and when in the agitator 1 Remove the barrel nut from the holder 2 Push down on plunger so that plunger threads extend beyond the metal barrel 3 Remove the assembly from the box 4 Thread colored hub into the threads in the plunger and finger tighten until snug 11 2 Procedure for SPME Sampiling with the PAL AutoSampler 5 Push the plunger back so that brass flange on the assembly is touching the metal barrel 6 Tilt holder so that the assembly needle is pointing upward vertical 7 Thread the assembly needle through the barrel nut by placing the nut over the vertical needle 8 Gently shake the holder until the nut slides down to the metal barrel Setting up the PAL Autosampler for SPME Refer to the Agilent GC Sampler 80 120 User Manual for installation of the PAL Autosampler and for setting the x y z parameters of the agitator tray holders trays and GC injectors FiberExp position In order for the SPME cycle to operate correctly it is necessary for the injection unit of the PAL Autosampler to be positioned next to the agitator just before the extraction This position has been designated as the Fibe
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