Application of a High Surface Area Solid-Phase Microextraction Air Sampling Device: Collection and Analysis of Chemical Warfare Agent Surrogate and Degradation Compounds

被引:10
|
作者
Stevens, Michael E., Jr. [1 ]
Tipple, Christopher A. [2 ]
Smith, Philip A. [3 ]
Cho, David S. [4 ]
Mustacich, Robert V. [5 ]
Eckenrode, Brian A. [2 ]
机构
[1] Fed Bur Invest Lab, Counterterrorism & Forens Sci Res Unit, Oak Ridge Inst Sci & Educ, Visiting Scientist Program, Quantico, VA 22135 USA
[2] Fed Bur Invest Lab, Counterterrorism & Forens Sci Res Unit, Quantico, VA 22135 USA
[3] Uniformed Serv Univ Hlth Sci, Dept Prevent Med & Biometr, Bethesda, MD 20814 USA
[4] Fed Bur Invest Lab, Counterterrorism & Forens Sci Res Unit, Oak Ridge Inst Sci & Educ, Quantico, VA 22135 USA
[5] Agilent Technol, Santa Clara, CA 95051 USA
关键词
CHROMATOGRAPHY-MASS-SPECTROMETRY; GAS-CHROMATOGRAPHY; O-ETHYL; VX; IDENTIFICATION; QUANTITATION; VOLATILES; STREAMS;
D O I
10.1021/ac401033a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This work examines a recently improved, dynamic air sampling technique, high surface area solid-phase microextraction (HSA-SPME), developed for time-critical, high-volume sampling and analysis scenarios. The previously reported HSA-SPME sampling device, which provides 10-fold greater surface area compared to commercially available SPME fibers, allowed for an increased analyte uptake per unit time relative to exhaustive sampling through a standard sorbent tube. This sampling device has been improved with the addition of a type-K thermocouple and a custom heater control circuit for direct heating, providing precise (relative standard deviation similar to 1%) temperature control of the desorption process for trapped analytes. Power requirements for the HSA-SPME desorption process were 30-fold lower than those for conventional sorbent-bed-based desorption devices, an important quality for a device that could be used for field analysis. Comparisons of the HSA-SPME device when using fixed sampling times for the chemical warfare agent (CWA) surrogate compound, diisopropyl methylphosphonate (DIMP), demonstrated that the HSA-SPME device yielded a greater chromatographic response (up to 50%) relative to a sorbent-bed method. Another HSA-SPME air sampling approach, in which two devices are joined in tandem, was also evaluated for very rapid, low-level, and representative analysis when using discrete sampling times for the compounds of interest. The results indicated that subparts per billion by volume concentration levels of DIMP were detectable with short sampling times (similar to 15 s). Finally, the tandem HSA-SPME device was employed for the headspace sampling of a CWA degradation compound, 2-(diisopropylaminoethyl) ethyl sulfide, present on cloth material, which demonstrated the capability to detect trace amounts of a CWA degradation product that is estimated to be less volatile than sarin. The rapid and highly sensitive detection features of this device may be beneficial in decision making for law enforcement, military, and civilian emergency organizations and responders, providing critical information in a contaminated environment scenario when time is of the essence.
引用
收藏
页码:8626 / 8633
页数:8
相关论文
共 50 条
  • [1] Chemical warfare agent (CWA) surrogate detection by metal-organic frameworks as solid-phase microextraction (SPME) material
    Swayze, Michael D.
    Riegner, Dawn E.
    Thomas, Mary Ann
    Lachance, Zach T.
    Kaplan, Sarah E.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2011, 241
  • [2] Solid-phase microextraction fiber development for sampling and analysis of volatile organohalogen compounds in air
    Attari, Seyed Ghavameddin
    Bahrami, Abdolrahman
    Shahna, Farshid Ghorbani
    Heidari, Mahmoud
    JOURNAL OF ENVIRONMENTAL HEALTH SCIENCE AND ENGINEERING, 2014, 12
  • [3] Solid-phase microextraction fiber development for sampling and analysis of volatile organohalogen compounds in air
    Seyed Ghavameddin Attari
    Abdolrahman Bahrami
    Farshid Ghorbani Shahna
    Mahmoud Heidari
    Journal of Environmental Health Science and Engineering, 12
  • [4] Air sampling and analysis of volatile organic compounds with solid phase microextraction
    Koziel, JA
    Pawliszyn, J
    JOURNAL OF THE AIR & WASTE MANAGEMENT ASSOCIATION, 2001, 51 (02) : 173 - 184
  • [5] Application of solid-phase microextraction to the analysis of volatile organic compounds in water
    Santos, FJ
    Galceran, MT
    Fraisse, D
    JOURNAL OF CHROMATOGRAPHY A, 1996, 742 (1-2) : 181 - 189
  • [6] Determination of chemical warfare agents and related compounds in environmental samples by solid-phase microextraction with gas chromatography
    Popiel, Stanislaw
    Sankowska, Monika
    JOURNAL OF CHROMATOGRAPHY A, 2011, 1218 (47) : 8457 - 8479
  • [7] Potential of solid-phase microextraction fibers for the analysis of volatile organic compounds in air
    Tuduri, L
    Desauziers, V
    Fanlo, JL
    JOURNAL OF CHROMATOGRAPHIC SCIENCE, 2001, 39 (12) : 521 - 529
  • [8] Application of solid-phase microextraction to the analysis of volatile compounds in virgin olive oils
    Jiménez, A
    Beltrán, G
    Aguilera, MP
    JOURNAL OF CHROMATOGRAPHY A, 2004, 1028 (02) : 321 - 324
  • [9] A simple calibration procedure for volatile organic compounds sampling in air with adsorptive solid-phase microextraction fibres
    Tuduri, L
    Desauziers, V
    Fanlo, JL
    ANALYST, 2003, 128 (08) : 1028 - 1032
  • [10] Analysis of Biogenic Volatile Organic Compounds in Air Using a Solid-Phase Extraction-Type Collection Device
    Ueta, Ikuo
    Fujikawa, Hiroto
    Fujimura, Koji
    Yoshimura, Tomotaka
    Narukami, Shoji
    Mochizuki, Suguru
    Sasaki, Tomohiro
    Maeda, Tsuneaki
    CHROMATOGRAPHY, 2018, 39 (01) : 27 - 32