• Spectroscopy and Spectral Analysis
  • Vol. 37, Issue 10, 3170 (2017)
WU Zhi-yuan1、*, YU Jian-wen1、2, LIU You-jiang1, and CHEN Chi-lai1
Author Affiliations
  • 1[in Chinese]
  • 2[in Chinese]
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    DOI: 10.3964/j.issn.1000-0593(2017)10-3170-05 Cite this Article
    WU Zhi-yuan, YU Jian-wen, LIU You-jiang, CHEN Chi-lai. The Solution of Non-Linear Function of Ion Mobility Based on FAIMS Spectrum Peak Position[J]. Spectroscopy and Spectral Analysis, 2017, 37(10): 3170 Copy Citation Text show less

    Abstract

    Volatile chlorobenzenes (CBs) is an organic pollutant which exists ubiquitously in the environment. Ion Mobility Spectrometry (IMS) has been a powerful technique for quick ion-separation and detection under ambient pressure. In this paper, atmospheric chlorobenzene, p-dichlorobenzene, o-dichlorobenzene and m-dichlorobenzene were detected by a homemade Vacuum Ultraviolet Field Asymmetric Waveform Ion Mobility Spectrometry (UV-FAIMS). The CV-I spectra under different Dispersion Voltage (DV) were obtained, then the CV-DV fingerprints spectra of the four substances were synthetized. Base on the fingerprint spectra, optimal separation and detection parameters of three isomers: dichlorobenzene, o-dichlorobenzene, m-dichlorobenzene were determined. The results showed that under the DV of 800 and 1 000 V, three substances could be effectively identified at CV of 20.4 V (DV=800 V), 3.2 V(DV=800 V) and 11.9 V(DV=1 000 V), respectively, by selecting the characteristic peaks. The influences of flow rate on FWHM and peak position of FAIMS spectrum were studied and the results provided a reference for flow optimization. The limit of detection (LOD) of UV-FAIMS investigated by using different concentrations of dichlorobenzene at DV=450 V and CV=4.3V was lower than 0.05 mg·m-3. This paper provides a rapid and accurate detection method for halogenated benzene pollutant and other isomers of benzene.
    WU Zhi-yuan, YU Jian-wen, LIU You-jiang, CHEN Chi-lai. The Solution of Non-Linear Function of Ion Mobility Based on FAIMS Spectrum Peak Position[J]. Spectroscopy and Spectral Analysis, 2017, 37(10): 3170
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