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Czasopismo
2005 | Vol. 35, nr 2 | 395-402
Tytuł artykułu

Rapid detection of trace chloroethylenes sing laser mass spectrometry

Wybrane pełne teksty z tego czasopisma
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Laser mass spectrometry is a new chemical trace analysis method with high selectivity, sensitivity and speed. The mass-resolved resonance-enhanced multiphoton ionization (REMPI) spectra of chloroethylenes-trichloroethylene and tetrachloroethylene are firstly reported in the range 305.0-325.0 nm. The mass-resolved excited spectra and laser power index of fragment ions CCl+ are presented. The experimental results indicate that 310.8 nm is the suitable ionization wavelength for detection of trichloroethylene and 322.5 nm for the detection of tetrachloroethylene in this wavelength range. The detection limits of these two chloroethylenes of concentration range expressed in ug/L are presented.
Wydawca

Czasopismo
Rocznik
Strony
395-402
Opis fizyczny
Bibliogr. 18 poz., wykr.
Twórcy
autor
  • Laboratory of Environmental Spectroscopy, Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, 230031 Hefei, China, majing@aiofm.ac.cn
autor
  • Laboratory of Environmental Spectroscopy, Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, 230031 Hefei, China
autor
  • Laboratory of Environmental Spectroscopy, Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, 230031 Hefei, China
autor
  • Laboratory of Environmental Spectroscopy, Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, 230031 Hefei, China
autor
  • Laboratory of Environmental Spectroscopy, Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, 230031 Hefei, China
autor
  • Laboratory of Environmental Spectroscopy, Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, 230031 Hefei, China
Bibliografia
  • [1] Oberg t., Neuer-Etscheidt K., Nordsieck H.O., Zimmermann R., Dioxin surrogates - a comparison of approaches, Organohalogen Compounds 59, 2002, pp. 37-44.
  • [2 ]Lemieus P.m., Lee C.W., Ryan J.V., Prediction of dioxin/furan incinerator emissions using low-molecular-weight volatile products of incomplete combustion, Journal of the Air and Waste Management Association 50(12), 2000, pp. 2129-37.
  • [3] Mahncke H.E., Noyes W.A., The ultraviolet absorption spectra of cis- and transdichloroethylenes, Journal of Chemical Physics 3(9), 1935, pp. 536-40.
  • [4] Berry M.J., Chloroethylene photochemical lasers: vibrational energy content of the HCl molecular elimination products, Journal of Chemical Physics 61(8), 1974, pp. 3114-43.
  • [5] Lake R.F., Thompson H., Photoelectron spectra of halogenated ethylenes, Proceedings of the Royal Society of London, Series A Mathematical and Physical Sciences 315(1522), 1970, pp. 323-38.
  • [6] Koerting C.F., Walzl K.N., Kuppermann A., A^n electron-impact investigation on the singlet to triplent transitions in the chloro-substituted ethylenes, Chemical Physics Letters 109(2), 1984, pp. 140-4.
  • [7] Robin M.B., Higher Excited Stages of Polyatomic Molecules, Academic, New York 1975, p. 2.
  • [8] Ibidem p. 50.
  • [9] Williams B.A., Cool T.A., Resonance ionization spectroscopy of the chloroethylenes, Journal of Physical Chemistry 97(7), 1993, pp. 1270-82.
  • [10] Zimmermann R., Herger H.J., Blumenstock M., Dorfner R., Schramm K.-W., Boesl U., Kettrup a., On-line measurement of chlorobenzene in waste incineration Hue gas as a surrogate for the emission of polychlorinated dibenzo-p-dioxins/furans (I-TEQ) using mobile resonance laser ionization time-of-Hight mass spectrometry, Rapid Communications in Mass Spectrometry 13(5), 1999, pp. 307-14.
  • [11] Mulberger F., Zimmermann R., Kettrup A., A mobile mass spectrometer for comprehensive on-line analysis of trace and bulk components of complex gas mixtures: parallel application of the laser-based ionization methods VUV single-photon ionization, resonant multiphoton ionization, and laser-induced electron impact ionization, Analytical Chemistry 73(15), 2001, pp. 3590-604.
  • [12] Boesl U., Laser mass spectrometry for environmental and industrial chemical trace analysis, Journal of Mass Spectrometry 35(3), 2000, pp. 289-304.
  • [13] Dorfner R., Ferge T., Yeretzian C., Kettrup A., Zimmermann R., Laser mass spectrometry as on-line sensor for industrial process analysis: process control of coffee roasting, Analytical Chemistry 76(5), 2004, pp. 1386-402.
  • [14] Dobashi S., Deguchi Y., Kubota T., Shinoda K., Real-time measurements of polychlorinated biphenyls using laser ionization time-of-Hight mass spectrometry, Analytical Sciences 20(1), 2004, pp. 13-8.
  • [15] Oser H., Copic K., Coggiola M.J., Faris G.W., Crosley D.R., Congener-specific detection of dioxins usingjet-REMPI, Chemosphere 43, 2001, pp. 469-77.
  • [16] Nakashima N., Yoshihara K., Role of hot molecules formed by internal conversion in UV single -photon andm^ultiphoton chemistry, Journal of Physical Chemistry 93(23), 1989, pp. 7763-71.
  • [17] Li Zi-yao, Xia Zhu-hong, Wei Jie, Gu Xue-jun, Zhang Bing, Calibration for trace gases detection with laser mass epectrometry, China Environmental Science 20, 2000, pp. 445-8.
  • [18] Wei Jie, Zhang Bing, Zheng Hi-yang, Zhang Lian-di, Kong Xiang-he, Xia Zhu-hong, Gu Xue-jun, Rapid analysis of trace pollutants using laser mass spectrometry, Science in China, Series A 44, 2001, pp. 940-6.
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.baztech-article-BWA0-0006-0026
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