Development of a PTR-TOFMS instrument for real-time measurements of volatile organic compounds in air

被引:54
|
作者
Tanimoto, Hiroshi
Aoki, Nobuyuki
Inomata, Satoshi
Hirokawa, Jun
Sadanaga, Yasuhiro
机构
[1] Natl Inst Environm Studies, Atmospher Environm Div, Tsukuba, Ibaraki 3058506, Japan
[2] Natl Inst Environm Studies, Asian Environm Res Grp, Tsukuba, Ibaraki 3058506, Japan
[3] Hokkaido Univ, Fac Environm Earth Sci, Sapporo, Hokkaido 0600810, Japan
关键词
proton transfer reaction; time-of-flight mass spectrometry; volatile organic compound; chemical ionization; PTR-MS; REACTION-MASS-SPECTROMETRY; ION FLOW TUBE; MS; H3O+; NO+; O-2(CENTER-DOT+); VALIDATION; EMISSIONS; QUALITY;
D O I
10.1016/j.ijms.2007.01.009
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
A proton transfer reaction-time-of-flight mass spectrometer (PTR-TOFMS) has been developed for real-time measurements of volatile organic compounds in air. The instrument is designed to be operated with a hollow cathode discharge ion source and an ion drift tube at relatively high pressures. Each component of the system, an ion source, a drift tube, an ion transfer region, and a time-of-flight mass spectrometer, are in detail characterized by a number of laboratory experiments. The optimized instrumental configuration enables us to gain high intensities of hydronium (H3O+) ions, typically similar to 7 x 10(5) counts for 1-min integration at a drift tube pressure of similar to 5 Torr. It also suppresses background signals, and interferences from sample air (NO+ and O-2(+)), which undergo fast reactions with volatile organic compounds, to similar to 0.5% of those of H3O+ ions. We find that the use of the custom-built discharge source show higher overall sensitivities than of a commercially available radioactive source. Potentials to detect oxygenated VOCs (aldehydes, ketones, and alcohols), halocarbons, and amines are also suggested. The detection limits for acetaldehyde, acetone, isoprene, benzene, toluene, and p-xylene were determined to be at the sub-ppbv levels for a 1-min integration time. A good linear response at trace levels is certified, but slight sensitivity dependency on water vapor contents is revealed. We finally demonstrate that the instrument can be used for on-line monitoring to detect large variations from emission sources in real-time. (c) 2007 Elsevier B.V. All rights reserved.
引用
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页码:1 / 11
页数:11
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