Application Note Monitoring VOCs in Ambient Air Using Sorbent Tubes with Analysis by TD-GC/MS in Accordance with Chinese EPA Method HJ -3 Application Note Abstract This application note demonstrates the excellent performance offered by Markes International s automated cryogen-free thermal desorption (TD) system for the analysis of volatile organic compounds (VOCs) in ambient air, sampled using sorbent tubes. The system used is compliant with Chinese EPA Method HJ 3, and features automated quantitative re collection of split flows, which allows repeat analysis, method development, and results verification. Introduction Volatile organic compounds (VOCs) are important precursors for atmospheric photochemical reactions, including those that generate low-level ozone and particulate matter that give rise to poor air quality. In addition, some of these VOCs are harmful to health in their own right, and these air toxics or hazardous air pollutants (HAPs) are therefore monitored in many industrial and urban environments. They range in volatility from chloromethane (methyl chloride) and acetone to hexachlorobutadiene and dodecene, and include polar as well as nonpolar compounds. Several national and international standard methods have been developed for air toxics and related applications, including US EPA Methods TO-5 (canisters) and TO-7 (sorbent tubes). In China, the Twelfth Five-Year Plan () emphasises the need to deepen the prevention and control of particulate matter pollution, and strengthen the control of volatile organic pollutants and toxic emissions. Control of VOCs has therefore become a priority in recent years, as reflected by the 3 Atmospheric Pollution Control Act and standard method HJ -3, released by the Chinese Ministry of Environmental Protection (MEP), and titled Ambient air Determination of volatile organic compounds Sorbent adsorption and thermal desorption gas chromatography mass spectrometry method.
In response to demand for measurement of air toxics, analytical technologies have been developed that offer an automated platform compliant with sorbent-tube-based methods. In this application note, we describe the sampling of VOCs in ambient air using sorbent tubes, followed by HJ -compliant analysis using an automated, cryogen-free thermal desorption-gas chromatography-mass spectrometry (TD-GC/MS) system. Background of thermal desorption Thermal desorption (TD) is a versatile GC preconcentration technology used to analyze volatile and semivolatile organic compounds (VOCs and SVOCs) in a wide range of sample types. By concentrating organic vapors from a sample into a very small volume of carrier gas (Figure ), TD maximizes sensitivity for trace-level target compounds, helps minimize interferences, and routinely allows analyte detection at the ppb level or below. It also greatly improves sample throughput by allowing full automation of sample preparation, desorption/extraction, preconcentration, and GC injection. The xr range of TD instruments from Markes International enhances these capabilities, offering a wide analyte range (C -C including reactive species), automated re-collection and reanalysis of split portions for method validation and compliance with standard methods, optional internal standard addition for improved confidence in results, and electronic/manual options for control of carrier gas. In this study, we use the TD-xr for fully automated analysis of up to sorbent tube samples. Experimental Standard A -component gas standard in nitrogen (which includes the 3 target compounds in HJ ), carried in pure helium, was loaded onto the sorbent tubes using a Calibration Solution Loading Rig (Markes International). Table. Instrumental parameters. A B Tube desorption and inlet split: Sample tube heated in a flow of carrier gas and analytes swept into an electrically cooled focusing trap, typically held between ambient and 3 C. Trap desorption and outlet split: Focusing trap rapidly heated (up to C/s) in a reverse flow of carrier gas (backflush operation), to transfer the analytes to the GC column. Sample tube Sample tubes and traps can contain multiple sorbents, for analysis of an extended range of analytes. Focusing trap Focusing trap Split/re-collection tube During either stage, the flow of analytes can be split and re-collected onto a clean sorbent tube. Split/re-collection tube To GC Parameter Value Real air sample Pumped sampling: ACTI-VOC (Markes International) Flow rate: 5 ml/min for minutes (total volume L) TD Instrument: TD-xr (Markes International) Tube: Universal (Markes International part no. C3-AXXX-5) Trap: Air toxics (Markes International part no. U-T5ATA-S) Tube dry-purge:. minutes Tube desorb: C ( minutes) Trap low: 5 C Trap heating rate: C/s Trap high: C for 3 minutes TD flow path: C GC Carrier gas: Helium GC column: Agilent J&W DB-, m.8 mm,. µm Mode: Constant-flow,. ml/min Oven ramp: 35 C (3 minutes), then 5 C/min to 9 C ( minutes) MS Ion source: 5 C Quadrupole: 5 C Transfer line: C Full scan range: m/z 35-3 Figure. How two-stage thermal desorption works.
Results and Discussion Chromatography Figure shows the chromatogram obtained for a sample equivalent to L of a ppbv standard. Excellent peak shape was obtained for all analytes, as illustrated for the challenging polar compound trichloromethane (expanded peak). These sharp peaks resulted from the rapid desorption of the focusing trap in the TD instrument, and are maintained even with splitless analysis, ensuring optimum sensitivity for trace-level analytes. Linearity System linearity was assessed by analyzing a variety of VOCs at.5,,, 5, and 9 ppbv (equivalent to a L sampling volume, and consistent with ambient concentrations). All R values were above.99 (Figure 3 and Table ). 8 Peak area,,-trichloro-,,-trifluoroethane (#) Benzene (#) Toluene (#5) Benzyl chloride (#3),-Dichloroethane (#5) Figure 3. Linearities for five key compounds from the standard. R.998.998.99.995.9979 8 Concentration (ppbv, L equivalent) 8 3 Abundance 3* 5.8.9.9 7 9 8 3 8 5 7 9 3 5 7 3 9 3 8 3 33 3 5 7 8 9 3.,-Dichloroethene.,,-Trichloro-,,-trifluoroethane 3. Chloropropene*. Dichloromethane 5.,-Dichloroethane. cis -,-Dichloroethene 7. Trichloromethane 8.,,-Trichloroethane 9. Tetrachloromethane.,-Dichloroethane. Benzene. Trichloroethene 3.,-Dichloropropane. cis-,3-dichloropropene 5. Toluene. trans -,3-Dichloropropene 7.,,-Trichloroethane 8. Tetrachloroethene 9.,-Dibromoethane. Chlorobenzene. Ethylbenzene. m,p -Xylene 3 o-xylene. Styrene 5.,,,-Tetrachloroethane. -Ethyltoluene 7.,3,5-Trimethylbenzene * Chloropropene was not present in the standard mix used; the label indicates where it would be expected to elute. Figure. Chromatogram obtained for a sample equivalent to L of a ppbv standard, with the 3 target compounds listed in HJ labeled. The trichloromethane peak is expanded, showing excellent peak shape. 3 8.,,-Trimethylbenzene 9.,3-Dichlorobenzene 3.,-Dichlorobenzene 3. Benzyl chloride 3.,-Dichlorobenzene 33.,,-Trichlorobenzene 3. Hexachlorobutadiene
Table. Linearity, detection limit, and repeatability data for the target VOCs. Note that chloropropene (#3) was not present in the standard mix used, and that chlorobenzene (#) is obscured by the internal standard chlorobenzene-d 5, so quantitation was not possible. Analyte concentration (ppbv) Quant ion (m/z) Run Run Run 3 Run Run 5 Run Run 7 No. Compound t R (min) R Mean conc. (ppbv) Std. dev. (ppbv) Peak area RSD (%) LOD (ppbv),-dichloroethene.3.995..38.95.93.8.7.5...8.7,,-trichloro-,,- trifluoroethane..998 5.9.7....3.8....3 Dichloromethane 3.3.998 9.33.377.5.8.3.3.39..3 7.5.95 5,-Dichloroethane 3.88.9979 3.79..535.58.98.8.3.85.3 7.5. cis-,-dichloroethene.5.998.38.37..3.387.3.3.38.3 5.9.7 7 Trichloromethane.9.988 85..3.59.53.53.8.7.9.8 5.7.88 8,,-Trichloroethane 5.5.98 97.3.7.95.3.93.7..8. 5..9 9 Tetrachloromethane 5..98 7.3.3.359.35.3.39.3.33.8 5..5,-Dichloroethane 5.3.997 78.53.5.58.58.5.5.97.5.3.3. Benzene 5..998.53.5.588.58.5.53.99.53.3.3.8 Trichloroethene.7.99 3.5.58.578.57.53.59.53.5.3 5..95 3,-Dichloropropane.7.995 3.53.55...3.57.53.578.3.. cis-,3-dichloropropene.97.99 75...9.8.77..7.5.3.9.98 5 Toluene 7.7.99 9.53.55.575.557.5.5.7.58.3.8. trans-,3-dichloropropene 7.5.995 75.7..5.9.5.59.3.77.9..9 7,,-Trichloroethane 7..9959 97.53.53.583.578.57.535.5.58.7.9.85 8 Tetrachloroethene 7.77.99..7.99.8.73.9.7.5.3 5.. 9,-Dibromoethane 8..998 7.8.3.77.7.3.8.3.8..8.7 Ethylbenzene 8.9.99.537.53.58.5.55.5.87.537.3.. m,p-xylene 8.8.979.95.9.7.735.7.58.9.9.8.8.5 3 o-xylene 9.7.988.9.95.5.53.5.83.5.5.3..9 Styrene 9.9.988.89.95.53.53.5.8.5.5.3..98 5,,,-Tetrachloroethane 9.8.995 85.573.559....57.55.585.9.9.9 -Ethyltoluene.3.988.5.57.57.83.73.9.5.59.3 7..7 7,3,5-Trimethylbenzene..9799.5.8.5.9.75.3.5.3.3 7.8.3 8,,-Trimethylbenzene.5.985...8.5..7.383..3 7.. 9,3-Dichlorobenzene.7.989.7.55.739.98.9.5..75.39 5.8. 3,-Dichlorobenzene.78.978.7.3.733.77.9.9..77.37 5.5.7 3 Benzyl chloride.93.995 9.38.35.3.38.385.3.3.38. 7..83 3,-Dichlorobenzene..98.3.35.9.7.59..58.3.3 5.. 33,,-Trichlorobenzene.7.975 8.553.55.7..58.553.57.5.33 5.8. 3 Hexachlorobutadiene.89.959 5...57.7.37.9..8..9.
Repeatability and limits of detection Seven repeat analyses of a.5 ppbv gas standard ( L equivalent) were conducted, and showed excellent consistency of retention times (Figure ). Relative standard deviations (RSDs) of repsonses for all target compounds were below 8% (Table ), and limits of detection (LODs) were below.5 ppbv. Quantitative re-collection of split flows Markes TD instruments have the ability to re-collect samples by directing the split flow (which would otherwise carry excess sample to vent) onto a sorbent tube. This process of re-collection can either be onto the tube from which the sample was originally desorbed, or onto a clean tube. This process can be fully automated, and offers a significant advantage over solvent extraction, because it allows a single sample to be analyzed multiple times. Sample splitting and re-collection makes method validation easier, and more importantly, avoids the need to collect another sample should the analysis unexpectedly fail to proceed correctly. 7 Run 7 5 Run Abundance Run 5 3 Run Run 3 Run Run 3 5 7 8 9 3 Figure. Seven repeated analyses of the same.5 ppbv standard. The baseline of each chromatogram is offset by for clarity. 5
Figure 5 shows a repeat analysis of a gas standard equivalent to L at ppbv with a : split flow, illustrating quantitative re-collection over a wide range of volatilities. Note the consistency of peak position and shape. The accuracy of the analysis was also validated by loading a sorbent tube with ng benzene and ng toluene, and performing re-collection/analysis cycles with a split ratio of.5: after the initial analysis. This showed excellent consistency with the theoretical values (Figure ). 8 Abundance Original sample Re-collected sample Ratio of response (re-collection/original) Benzene Toluene Theoretical decay curve 8 8 Figure 5. Original analysis (black) and repeat analysis (red) of tubes containing analytes equivalent to L of a ppbv standard with a : outlet split. 3 5 7 8 9 Run number Figure. Evaluation of the decay in response for benzene and toluene from a tube repeatedly analyzed with a.5: outlet split.
Real air samples To evaluate the performance of the system for a real-world scenario, L of ambient air was collected onto a sorbent tube in an office, a laboratory, and semirural outside air, followed by analysis under the conditions described earlier. The results clearly show raised levels of VOCs in the office air (Figure 7). 5 3 Abundance 3 3 5 3 7 8 8 7 9 9 Office air 5 Laboratory air Semirural outside air 5 5 3 35. Methanol. -Methylbutane 3. Ethanol. Acetone 5. Isopropanol. -Methylpentane 7. 3-Methylpentane 8. Hexane 9. Ethyl acetate. -Methylhexane. Cyclohexane. Trimethylhexane 3. Heptane. Acetic acid 5. Butan--ol. Toluene 7. Hexanal 8. m- and p -Xylene 9. o-xylene. α-pinene. Cyclohexanone. α-myrcene 3. Limonene. Phenol 5. Menthol. -Phenoxyethanol Figure 7. Analysis of three L air samples collected at three different locations using sorbent tubes, and analyzed by TD-GC/MS. Compounds listed in HJ are marked in bold type. 7
Conclusions This application note demonstrates that Markes International s automated, cryogen-free thermal desorption systems offer excellent results for monitoring air toxics in ambient air in accordance with Chinese EPA Method HJ. A particular feature of this method is the automated quantitative re-collection of split flows offered by the TD instrument, which makes method development and validation of results straightforward. Trademarks ACTI-VOC, CSLR, and TD-xr are trademarks of Markes International. DB- is a trademark of Agilent Technologies. Applications were performed under the stated analytical conditions. Operation under different conditions, or with incompatible sample matrices, may impact the performance shown. For More Information These data represent typical results. For more information on our products and services, visit our Web site at www.agilent.com/chem. www.agilent.com/chem Agilent shall not be liable for errors contained herein or for incidental or consequential damages in connection with the furnishing, performance, or use of this material. Information, descriptions, and specifications in this publication are subject to change without notice. Agilent Technologies, Inc., 7 Printed in the USA July 7, 7 599-87EN