1982
DOI: 10.1021/ac00238a013
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Tunable selective detection for capillary gas chromatography by ion mobility monitoring

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Cited by 124 publications
(42 citation statements)
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References 17 publications
(12 reference statements)
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“…The fact that the mobility time of the solvent peaks increased with experimental duration suggested that the solvent ions were surrounded by an increasing amount of solvation molecules. Conventional gas phase ion mobility spectrometry has a unidirectional counter flow of drift gas that keep the drift region clean by continuously sweeping out neutral molecules [84]. Because the liquid hexane medium was stationary in this study, any uncharged solvent molecules would remain inside the spectrometer.…”
Section: Lpims Spectra Of Solvent Blankmentioning
confidence: 99%
“…The fact that the mobility time of the solvent peaks increased with experimental duration suggested that the solvent ions were surrounded by an increasing amount of solvation molecules. Conventional gas phase ion mobility spectrometry has a unidirectional counter flow of drift gas that keep the drift region clean by continuously sweeping out neutral molecules [84]. Because the liquid hexane medium was stationary in this study, any uncharged solvent molecules would remain inside the spectrometer.…”
Section: Lpims Spectra Of Solvent Blankmentioning
confidence: 99%
“…Several sources have been used as the primary ionization source, including thermionic emission, 22 flame ionization, 4 photoionization, 23 surface ionization 24 laser multiphoton ionization, 25 electrospray, 26 and corona-discharge. 27 Early IMS instrumentation sometimes involved other sources; 63 Ni was the ionization source in the first patent and is still used in some instruments today.…”
Section: Ionization Sourcementioning
confidence: 99%
“…16 The clearance-time problem in IMS was solved by Hill and co-workers when they constructed an IMS with a reduced ionization volume and introduced the concept of unidirectional flow in ion mobility spectrometry. 17 In the unidirectional flow design of IMS, the sample is introduced between the ionization region and the first ion gate of the spectrometer (see Figure 1). The IMS drift gas enters the spectrometer at the collector electrode end, flows completely through the spectrometer in one direction, counter to that of ion migration, and exits at the opposite end of the spectrometer, sweeping the neutral sample molecules into the ionization region and out of the spectrometer in minimal time.…”
Section: Portable Gc/imsmentioning
confidence: 99%