Optimization of Method Parameters for the Evaluation of USEPA Method Using a Purge and Trap with GC/MS

Similar documents
Roger Bardsley, Applications Chemist; Teledyne Tekmar P a g e 1

Exploring US EPA Method 524 Purge and Trap Variables: Water Vapor Reduction and Minimizing Cycle Time

Roger Bardsley, Applications Chemist; Teledyne Tekmar Page 1

Analytical Trap Comparison for USEPA Method 8260C

US EPA Method with the Tekmar Lumin P&T Concentrator, AQUATek LVA and Agilent 7890B GC/5977A MS

Solid Phase Micro Extraction of Flavor Compounds in Beer

Maximizing Sample Throughput In Purge And Trap Analysis

US EPA Method 8260 with the Tekmar Atomx XYZ P&T System and Agilent 7890B GC/5977A MS

Optimal VOC Method Parameters for the StratUm PTC Purge & Trap Concentrator

Validation of USEPA Method Using a Stratum PTC, AQUATek 100 Autosampler, and Perkin-Elmer Clarus 600 GC/MS

Analysis of Volatile Organic Compounds in Soil Samples by EPA Method 8260 with The Stratum PTC and SOLATek 72 Multi-Matrix Autosampler

Analysis of Volatile Organic Compounds Using USEPA Method 8260 and the 4760 Purge and Trap and the 4100 Autosampler

Validation of USEPA Method 8260C Using Teledyne Tekmar Atomx, and Perkin-Elmer Clarus 600 GC/MS

Using Hydrogen as An Alternative Carrier Gas for US EPA 8260

Optimization of 1,4-Dioxane and Ethanol Detection Using USEPA Method 8260 Application Note

Methanol Extraction of high level soil samples by USEPA Method 8260C

Analysis of Volatile Organic Compounds in Water and Soil by EPA Method 8260 with the Atomx Concentrator/Multimatrix Autosampler

A Comparison of Volatile Organic Compound Response When Using Nitrogen as a Purge Gas

Optimizing. Abstract: is standardd. procedures. altered to

Validation of Volatile Organic Compound by USEPA. Method 8260C. Application Note. Abstract. Introduction. Experimental-Instrument Conditions

Validation of USEPA Method Using a Stratum PTC and the New AQUATek 100 Autosampler

System and JUREK ANNE. Introduction: in an in purge and. trap sampling. Discussion: As part of. consistent and reliable data. (MoRT) to.

INNOVATIVE PRODUCTS, SUPERIOR SUPPORT. Presenter: Anne Jurek, Senior Applications Chemist, EST Analytical

Analysis. Introduction: necessary. presented. Discussion: As part of be carried. consistent and reliable data. (MoRT) to.

ANNE JUREK. Abstract: soils and are found. in can also with GC/MS. poster. in series. option for. There are problems. analytes. in methanol.

Validation of Environmental Water Methods on One System: Considerations for Sample Volume, Purge Parameters and Quality Control Parameters

TO-17 Extending the Hydrocarbon Range above Naphthalene for Soil Vapor and Air Samples Using Automated

Application Note. Abstract. Introduction. Experimental-Instrument Conditions. By: Anne Jurek

Method 8260C by Purge and Trap Gas Chromatography Mass Spectrometry using the Clarus SQ 8

Application Note. Abstract. Introduction. Experimental-Instrument Conditions. By: Anne Jurek

Performance of a Next Generation Vial Autosampler for the Analysis of VOCs in Water Matrices

Analysis of Geosmin and 2-Methylisoborneol Utilizing the Stratum PTC and Aquatek 70

Determination of Volatile Organic Compounds in Air

Evaluation of a New Analytical Trap for Gasoline Range Organics Analysis

U.S. EPA VOLATILE ORGANICS METHOD USING PURGE AND TRAP GC/MS

2017 EPA Method Update Rule and EPA Method 624.1

Analysis of Low Level Volatile Organic Compounds in Air Anne Jurek

Optimal Conditions for USEPA Method 8260B Analysis using the EST Analytical Sampling system and the Shimadzu GCMS-QP2010s

Optimizing of Volatile Organic Compound Determination by Static Headspace Sampling

Roger Bardsley, Applications Chemist; Teledyne Tekmar Page 1

Optimizing Standard Preparation

Volatile Organic Compounds in Every Day Food

Copyright 2009 PerkinElmer LAS and CARO Analytical Services, Inc.

UCMR 3 Low-Level VOC Analysis by Purge and Trap Concentration and GC/MS using Selective Ion Monitoring

Validation of New VPH GC/MS Method using Multi-Matrix Purge and Trap Sample Prep System

A Single Calibration Method for Water AND Soil Samples Performing EPA Method 8260

Maximizing Production While Minimizing Costs

A Comparative Analysis of Fuel Oxygenates in Soil by Dynamic and Static Headspace Utilizing the HT3 TM Automatic Headspace Analyzer

A Single Calibration for Waters and Soil Samples Performing EPA Method Anne Jurek Applications Chemist

Ed George and Anaïs Viven Varian, Inc.

STANDARD OPERATING PROCEDURES

Application Note. Application Note 081 Innovative Cryogen-Free Ambient Air Monitoring in Compliance with US EPA Method TO-15. Abstract.

AUTONOMOUS, REAL TIME DETECTION OF 58 VOCS IN THE PANAMA CANAL

Measuring Environmental Volatile Organic Compounds by U.S. EPA Method 8260B with Headspace Trap GC/MS

Reactions of Vinyl Chloride and Methanol in a Quadrupole Ion Trap Mass Spectrometer during VOC Analysis

Chemistry Instrumental Analysis Lecture 27. Chem 4631

Thermal Desorption Technical Support

Solid Phase Microextraction of Cyanogen Chloride and Other Volatile Organic Compounds in Drinking Water with Fast Analysis by GC-TOFMS

Amy Nutter, Applications Chemist; Teledyne Tekmar P a g e 1

Optimizing Conditions for Volatiles Analysis

Detection of Volatile Organic Compounds in polluted air by an Agilent mini Thermal Desorber and an Agilent 5975T LTM GC/MS

Solid Phase Micro Extraction of Flavor Compounds in Beer

Application News AD Quantitative Determination of Volatile Organic Compounds in Drinking Water by EPA Method with Headspace Trap GC-MS

Applying the Technology of the TurboMatrix 650 ATD to the Analysis of Liquid Accelerants in Arson Investigation

Helium conservation in volatile organic compound analysis using U.S. EPA Method 8260C

Headspace Technology for GC and GC/MS: Features, benefits & applications

Determination of VOCs by USEPA Method 8260 with Extended Dynamic Range using Fast, Sensitive Capillary GC/MS

Reduced VOC Sample Analysis Times Using a New Dual Purge-and-Trap System

Rapid Determination of TO-15 Volatile Organic Compounds (VOCs) in Air

Practical Faster GC Applications with High-Efficiency GC Columns and Method Translation Software

Chromatography. Gas Chromatography

Meeting NJ Low Level TO-15 Air Testing Method Requirements

Improved Volatiles Analysis Using Static Headspace, the Agilent 5977B GC/MSD, and a High-efficiency Source

METHOD 5021 VOLATILE ORGANIC COMPOUNDS IN SOILS AND OTHER SOLID MATRICES USING EQUILIBRIUM HEADSPACE ANALYSIS

AN INTEGRATED SYSTEM USING TEMPERATURE BASED SAMPLING FOR POLYMER CHARACTERIZATION

1,2-Dibromoethane (EDB) and 1,2-dibromo-3-chloropropane (DBCP), gas chromatography, microextraction

Application Note 116 Monitoring VOCs in Ambient Air Using Sorbent Tubes with Analysis by TD-GC/MS in Accordance with Chinese EPA Method HJ

Analysis of Residual Solvents in Pharmaceuticals (USP<467>) with Shimadzu GC-2010 Plus and HS-10 Headspace Sampler

VOC Analysis of Water-Based Coatings by Headspace-Gas Chromatography

Activity in the FID Detection Port: A Big Problem if Underestimated

EPA TO-17 Volatile Organic Compounds

Enhanced Method Detection Limits for irm-gc/ms of Volatile Organic Compounds Using Purge and Trap Extraction

Determination of Total Volatile Organic Compounds in Indoor Air Using Agilent 7667A mini TD and 7820A GC

CALA Directory of Laboratories

Selection of a Capillary

Determination of Volatile Aromatic Compounds in Soil by Manual SPME and Agilent 5975T LTM GC/MSD

VUV ANALYTICS VGA-100 GC DETECTOR Gas Chromatograph Agilent 6890 equipped with a 7683 model autosampler Restek 30m x 0.25mm x 0.

Low-Level Sulfur Compounds in Beer by Purge and Trap with a Pulsed Flame Photometric Detector (PFPD)

Study of Residual Solvents in Various Matrices by Static Headspace

ANALYTICAL REPORT. Results relate only to the items tested and the sample(s) as received by the laboratory. Page 1 of 5

Selection of a Capillary GC Column

An Advanced Base Deactivated Capillary Column for analysis of Volatile amines Ammonia and Alcohols.

ELECTRONICALLY REPRINTED FROM. Volume 34 Number 3 MARCH

THE NEW QUANTITATIVE ANALYTICAL METHOD FOR ULTRATRACE SULFUR COMPOUNDS IN NATURAL GAS

Thermal Desorption Technical Support

ANALYTICAL REPORT. Job Number: Job Description: Transform Complete

USP <467> Headspace Residual Solvent Assay with a HT3 Headspace Instrument

Identifying Pesticides with Full Scan, SIM, µecd, and FPD from a Single Injection Application

Highly Sensitive and Rugged GC/MS/MS Tool

Volatile organic compounds (VOCs):

Transcription:

Application Note Optimization of Method Parameters for the Evaluation of USEPA Method 524.2 Using a Purge and Trap with GC/MS Objective By: Glynda Smith In this paper, an evaluation of different methods of moisture control will be presented and the Tekmar-Dohrmann 3 Sample Concentrator will be optimized for the analysis of the USEPA 524.2 compound list using GC/MS. This optimization of method parameters will focus on achieving the optimal chromatographic response by reducing the effect of water on the analysis. Introduction Purge and Trap coupled with gas chromatography offers a simple method for the extraction and concentration of volatile organic compounds (VOCs) from multiple matrices such as waters and soils. USEPA Method 524.2 monitors a wide range of VOCs in drinking water. Due to the range and number of compounds analyzed in Method 524.2, there are several analytical problems that can arise. One of the most common problems involves the transfer of water to the analytical column. Excessive water transfer can cause problems with both the mass spectrometer and the chromatography. A mass spectrometer is especially sensitive to the presence of water. Various types of vacuum pumps may be incorporated (e.g., roughing pumps, turbomolecular pumps, diffusion pumps, etc.) and the pumping efficiencies can vary with time and with the level of maintenance. The pressure load that water imposes upon a mass spectrometer interferes with the efficiency of electron ionization, shortens the lifetime of the filaments, and results in higher maintenance costs. With respect to the chromatography, excess water often produces unacceptable broadening of early eluting peaks. Removal of water can be facilitated through the use of hydrophobic trapping materials and incorporation of a moisture control system (MCS) which condenses water from the desorb gas during the transfer to the gas chromatograph. The research described in this paper involves the evaluation of the moisture control system and two types of traps under varying conditions of sample mount temperatures, MCS temperatures, dry purge times, and desorb times. Experimental Method 524.2 Rev. 4 standards were obtained from Restek Corp. (VOA Kit - Cat #3447). Duplicate data runs employed 5 ml samples containing ppb of each of the analytes. The parameters evaluated are as follows: I. Vocarb 3 Hydrophobic Trap A. Moisture Control System (MCS) Installed. Vary 2. Vary Dry Purge 3. Vary Mount Temperature 4. Vary Desorb B. MCS Uninstalled. Vary Dry Purge 2. Vary Mount Temperature 3. Vary Desorb II. #3 (Tenax/Charcoal/Silica Gel) Hydrophilic Trap A. Moisture Control System (MCS) Installed. Vary 2. Vary Mount Temperature 3. Vary Desorb B. MCS Uninstalled. Vary Mount Temperature 2. Vary Desorb 3-.doc; 9-Jun-3 Sales/Support: 8-874-24 Main: 53-229-7 4736 Socialville Foster Rd., Mason, OH 454 www.tekmar.com

The Tekmar-Dohrmann 3 Purge & Trap Sample Concentrator parameters that were held constant throughout all of the data runs are described below: Line Temperature 5 C Trap Pressure Control 4 psi Valve Temperature 5 C Bake 2 min. Purge Ready Temp. 35 C Bake Temperature 27 C (Vocarb);23 C () Purge min. Desorb Temperature 25 C (); 225 C () Desorb Preheat 245 C (); 22 C () Table. Conditions for HP 689GC/5973 MS Injector: Column: Temperature Program: Carrier: C, Split 2: with Vocarb trap; Split 5: with #3 trap Restek Corp. Rtx-VMS, 6m x.25mm x.4µm 45 C (hold min). Increase to 9 C at 2 C/min and hold 2 min. at 9 C. Increase to 225 C at 6 C/min and hold min. at 225 C. Helium,.2 ml/min MS Source Temperature: 23 C MS Quad Temperature: 5 C Electron Multiplier: Mass Range Scanned: Vacuum System: 62 volts 35-26 amu Turbomolecular pump, maintained @.2 x -5 Torr Splitting at the injection port is a good technique for water removal. A 5: split was needed for samples that were run on the hydrophilic #3 trap in order to fully resolve the light gases. When lower split ratios were examined, the higher baselines and broadened peak shapes of the early eluting components resulted in wide variability for the calculated response factors of the light gases. The Vocarb 3 trap, however, is very effective at removing water due to its hydrophobicity. As such, a lower 2: split ratio provided sufficient chromatographic resolution for samples prepared with the Vocarb 3 trap. Results and Discussion Tables 2 through 8 list the response factors obtained for a group of representative compounds under the conditions described in Table. All six of the gas standards are included (dichlorodifluoromethane, chloromethane, vinyl chloride, bromomethane, trichlorofluoromethane) along with three mid-boiling range compounds (methyl acrylate, toluene, pentachloroethane) and three high boiling range compounds (,2,4- trichlorobenzene, naphthalene,,2,3-trichlorobenzene). Vary Table 2.. Vary during Desorb Vocarb 3 Trap Analyte 4 C 5 C 6 C Analyte 4 C 5 C 6 C Dichlorodifluoromethane.49.44.4 Dichlorodifluoromethane.26.97.237 Chloromethane.277.5.286 Chloromethane.33.22.296 Vinyl Chloride.286.288.293 Vinyl Chloride.52.2.5 Bromomethane.87.95.24 Bromomethane.69.236.68 Chloroethane.42.36.47 Chloroethane.47.64.43 Trichlorofluoromethane.48.486.497 Trichlorofluoromethane.229.234.8 Methyl Acrylate.35.34.38 Methyl Acrylate.8.85. Toluene.6.56.55 Toluene.78.47.55 Bromoform.286.269.288 Bromoform.226.223.232 Pentachloroethane.36.356.379 Pentachloroethane.38.295.35,2,4-Trichlorobenzene.97.885.896,2,4-Trichlorobenzene.783.742.764 Naphthalene.43.295.444 Naphthalene.95.34.52,2,3-Trichlorobenzene.856.89.84,2,3-Trichlorobenzene.73.676.76 Table 2 shows the results obtained when the MCS temperature was increased during the desorb cycle. The MCS is typically cooled to ambient temperature during the desorb step in order to condense water prior to transfer of 3-.doc; 9-Jun-3 Page 2 of 7

the analytes from the trap to the GC. As the data indicates, the overall responses are higher with the Vocarb 3 trap relative to the #3 trap. Specifically, the average responses of the lighter components are about 8% better with the Vocarb trap. This is not surprising since the early eluting components are adversely affected by the presence of water. But for either trap, there is little variation in the analyte responses as a function of MCS temperature and there seems to be no analytical advantage in operating the system at elevated MCS temperatures. Graph provides a brief synopsis of this information showing the effect on two of the gas standards, a mid-boiling range compound and a high boiling range compound. Graph..5.4.3.2. Vary - Dichlorodifluoromethane 5 Vary - Chloroethane.2.5..5 5 Vary - Toluene Vary - Naphthalene.5..5 5 2.5.5 5 Vary Dry Purge Hydrophobic traps such as the Vocarb 3 trap can be purged with dry gas prior to desorption of the sample. This step facilitates water removal. Hydrophilic traps, however, do not benefit from incorporation of a dry purge since water will preferentially remain in the silica gel. Thus, the data in tables 3 and 4 only refer to the Vocarb 3 trap. Table 3.. Vary Dry Purge (Applies to Vocarb 3 Trap Only) Vocarb 3 Trap Analyte min. 2 min. 4 min. 6 min. 8 min. Dichlorodifluoromethane.536.58.596.545.53 Chloromethane.322.332.327.348.329 Vinyl Chloride.38.324.352.328.325 Bromomethane.23.247.244.236.22 Chloroethane.65.67.68.65.67 Trichlorofluoromethane.66.593.642.67.628 Methyl Acrylate.22.25.27.9.38 Toluene.85.5.56.53.47 Bromoform.296.289.29.29.283 Pentachloroethane.355.362.378.368.355,2,4-Trichlorobenzene.93.9.95.9.93 Naphthalene.468.453.432.39.372,2,3-Trichlorobenzene.864.855.858.85.845 3-.doc; 9-Jun-3 Page 3 of 7

Table 4.. Vary Dry Purge Vocarb 3 Trap Analyte min. 2 min. 4 min. 6 min. 8 min. Dichlorodifluoromethane.394.393.376.347.4 Chloromethane.275.28.278.263.23 Vinyl Chloride.287.292.29.269.337 Bromomethane.223.238.238.23.22 Chloroethane.85.78.53.65.92 Trichlorofluoromethane.59.595.59.562.69 Methyl Acrylate.22.26.99.24. Toluene.2.954.952.825.68 Bromoform.247.243.253.237.274 Pentachloroethane.37.326.327.35.387,2,4-Trichlorobenzene.699.764.773.72.856 Naphthalene.2.8.53.28.239,2,3-Trichlorobenzene.653.7.729.67.82 When a moisture control system is installed along with a hydrophobic trap such as the Vocarb 3, a dry purge step may or may not be beneficial and the length of time employed should be determined by the application. In the work described in this paper, the split ratios employed minimized the dry purge effect. When the MCS is bypassed inside the valve oven with a short piece of /6 Silcosteel tubing, however, a long dry purge step is needed in order to attain the same analyte responses as when the MCS is incorporated in the sample pathway (see Graph 2). Graph 2. Vary Dry Purge - Dichlorodifluoromethane Vary Dry Purge - Vinyl Chloride.4.8.6.4.2 5.3.2. 5 Vary Dry Purge - Bromoform Vary Dry Purge - Naphthalene.35.3.25.2.5..5 5 2.5.5 5 3-.doc; 9-Jun-3 Page 4 of 7

Vary Mount Temperature Tables 5 and 6 compare the results obtained at different mount temperatures when the MCS is installed and removed, respectively. Table 5.. Vary Mount Temperature Vocarb 3 Trap Analyte Ambient 75 C C Analyte Ambient 75 C C Dichlorodifluoromethane.54.47.53 Dichlorodifluoromethane.2.47.37 Chloromethane.323.37.329 Chloromethane.292.9.268 Vinyl Chloride.32.35.325 Vinyl Chloride.7.2.73 Bromomethane.2.228.22 Bromomethane.28.7.6 Chloroethane.64.56.67 Chloroethane.7.65.4 Trichlorofluoromethane.6.582.628 Trichlorofluoromethane.327.293.34 Methyl Acrylate..26.38 Methyl Acrylate.7.76.5 Toluene.37.27.47 Toluene.96.53.89 Bromoform.265.29.283 Bromoform.29.29.22 Pentachloroethane.353.359.355 Pentachloroethane.29.297.298,2,4-Trichlorobenzene.722.96.93,2,4-Trichlorobenzene.539.762.756 Naphthalene.873.425.372 Naphthalene.565.52.3,2,3-Trichlorobenzene.598.867.845,2,3-Trichlorobenzene.293.678.688 Table 6.. Vary Mount Temperature Vocarb 3 Trap Analyte Ambient 75 C C Analyte Ambient 75 C C Dichlorodifluoromethane.379.356.4 Dichlorodifluoromethane.28.32.27 Chloromethane.36.296.23 Chloromethane.22.7.98 Vinyl Chloride.32.38.337 Vinyl Chloride.28.53.85 Bromomethane.243.244.22 Bromomethane.239.88.23 Chloroethane.92.79.92 Chloroethane.79.52.7 Trichlorofluoromethane.66.636.69 Trichlorofluoromethane.225.388.265 Methyl Acrylate..6. Methyl Acrylate.67.88.2 Toluene.3.7.68 Toluene.975.83.797 Bromoform.255.269.274 Bromoform.223.223.238 Pentachloroethane.35.358.387 Pentachloroethane.287.295.294,2,4-Trichlorobenzene.652.87.856,2,4-Trichlorobenzene.349.43.467 Naphthalene.72.336.239 Naphthalene.353.524.645,2,3-Trichlorobenzene.58.839.82,2,3-Trichlorobenzene.2.42.444 Elevated sample mount temperature eliminates a cold spot at the top of the glassware. On average, increasing the mount temperature from ambient conditions to 75 C results in a 6% increase in the response factors for the heavier components without sacrificing the response of the early eluting gases. Furthermore, the data clearly indicates that removal of the MCS results in the loss of analyte response on the hydrophilic #3 trap. For example, with the MCS removed, the response factor for naphthalene drops by 5% as shown in Graph 3. Graph 3. Vary Mount Temperature - Naphthalene s.5.5 25 5 75 25 Temperature ( C) - Vocarb - Vocarb - - 3-.doc; 9-Jun-3 Page 5 of 7

Vary Desorb Tables 7 and 8 compare the results obtained at different desorb times when the MCS is installed and removed, respectively. Table 7.. Vary Desorb Vocarb 3 Trap Analyte 2 min. 4 min. 6 min. 8 min. Analyte 3 sec. min. 2 min. 4 min. Dichlorodifluoromethane.47.44.424.454 Dichlorodifluoromethane.99.46.64.48 Chloromethane.269.329.232.2 Chloromethane.36.27.63.2 Vinyl Chloride.284.288.34.33 Vinyl Chloride.296.2.3.24 Bromomethane.94.95.25.27 Bromomethane.227.6.247.25 Chloroethane.4.36.5.6 Chloroethane.6.76.6.94 Trichlorofluoromethane.545.486.565.62 Trichlorofluoromethane.29.48.454.468 Methyl Acrylate.22.34.2.57 Methyl Acrylate.8.8.79.69 Toluene.56.56.7.22 Toluene.22.76.9.992 Bromoform.275.269.276.277 Bromoform.237.22.247.255 Pentachloroethane.34.356.345.363 Pentachloroethane.32.294.32.349,2,4-Trichlorobenzene.77.885.884.883,2,4-Trichlorobenzene.77.748.79.82 Naphthalene.93.295.4.488 Naphthalene.62.32.45.44,2,3-Trichlorobenzene.72.89.82.83,2,3-Trichlorobenzene.77.68.73.735 Table 8.. Vary Desorb Vocarb 3 Trap Analyte 2 min. 4 min. 6 min. 8 min. Analyte 3 sec. min. 2 min. Dichlorodifluoromethane.39.4.369.327 Dichlorodifluoromethane.84.79.72 Chloromethane.39.23.347.35 Chloromethane.6.75.87 Vinyl Chloride.347.337.357.33 Vinyl Chloride.63.42.22 Bromomethane.279.22.28.26 Bromomethane.29.244.85 Chloroethane.83.92.22.99 Chloroethane.6.49.69 Trichlorofluoromethane.732.69.697.646 Trichlorofluoromethane.299.23.556 Methyl Acrylate.44..65.34 Methyl Acrylate.7.98.97 Toluene.5.68.4.7 Toluene.973.767.854 Bromoform.33.274.285.268 Bromoform.33.252.246 Pentachloroethane.399.387.374.363 Pentachloroethane.42.36.35,2,4-Trichlorobenzene.863.856.868.858,2,4-Trichlorobenzene.797.497.459 Naphthalene.82.239.34.336 Naphthalene.43.667.638,2,3-Trichlorobenzene.82.82.87.8,2,3-Trichlorobenzene.86.47.442 When the hydrophobic Vocarb 3 trap is installed, variations in desorb time between 2 8 minutes do not significantly affect analyte response. The hydrophilic #3 trap, however, shows a better overall response with a shorter desorb time. Longer desorb times yield poor chromatography with the early eluting components, i.e., higher baselines with broadened peaks due to the excess water that is also desorbed onto the column. The result is wide variability in the calculated response factors. Thus, it was deemed unnecessary to examine desorb times longer than 4 minutes with the #3 trap. Also, a longer desorb time in conjunction with removal of the moisture control system further compounds the problem for the #3 trap because the responses of the later eluting analytes begin to show significant variability. Graph 4 provides a graphical summary of this information. 3-.doc; 9-Jun-3 Page 6 of 7

Graph 4. Vary Desorb - Vinyl Chloride Vary Desorb - Vinyl Chloride.5.4.3.2. 5 - -.4.3.2. 5 - #3 - #3 Vary Desorb - Toluene Vary Desorb - Naphthalene.3..9.7.5 5 - -.5.5 5 - - In general, incorporation of a moisture control system (MCS) appears to help with water removal. When the MCS is installed and a Vocarb 3 trap is used, a dry purge step can be minimized. With the MCS removed, however, a dry purge is needed in order to obtain responses similar to those observed when it is installed. The MCS also provides better consistency in the data obtained with the #3 trap. When the MCS is removed, the responses tend to drop because this trap is holds water in the silica gel layer and allows the water to be desorbed to the GC. The data further indicates that a heated mount feature, such as that provided on the Tekmar 3 Sample Concentrator, provides excellent responses for the heavier components in the 524.2 Compound List when it is maintained at an elevated temperature. Conclusions Excess water can pose difficulties in purge & trap analyses. But using the combination of a dry purgeable trap, a moisture control system, split injection, and a heated mount provides maximum reduction of water that gets transferred to the column. Figures and 2 provide quick references to the best conditions for water removal with a Vocarb 3 trap and a #3 trap, respectively. Figure. Purge & Trap Conditions for Vocarb 3 Trap Figure 2. Purge & Trap Conditions for 3-.doc; 9-Jun-3 Page 7 of 7