Proton transfer mass spectrometry at 11 hPa with a circular glow discharge: Sensitivities and applications

被引:17
作者
Hanson, D. R. [1 ]
Koppes, M. [1 ]
Stoffers, A. [1 ]
Harsdorf, R. [1 ]
Edelen, K. [1 ]
机构
[1] Augsburg Coll, Dept Chem, Minneapolis, MN 55454 USA
基金
美国国家科学基金会;
关键词
Proton transfer mass spectrometry; Volatile organic compounds; Glow discharge; Fragmentation; VOLATILE ORGANIC-COMPOUNDS; PTR-MS; CALIBRATION; ATMOSPHERE; ISOPRENE; ACID;
D O I
10.1016/j.ijms.2009.01.021
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
The design and testing of a circular glow discharge ion source on a custom built proton transfer mass spectrometer are described. Also, issues important for quantitative measurements of volatile organic compounds using this instrument were investigated. Detailed calibration procedures based on gravimetry are presented, and representative outdoor air data are shown. Calibrations yield a good sensitivity, up to a few Hz/pptv for some compounds, and the detection limit (S/N = 3) is similar to 100 pptv or better for methanol, acetaldehyde and acetone (5 s sampling time with a 5 s zero). Detection limits are much lower for most other compounds due to high sensitivity and low background. For ions with m/z > similar to 90 the background signals are very low and species that appear efficiently at these m/z can be detected at the 10 pptv level in a few seconds. Ion breakup processes for alcohols show that a major product ion of mono-functional alcohols is at 57 u, presumably C(4)H(9)(+). Oxalic acid is an interesting case in that a major product ion appears on an even mass, 46 u, presumably CO(2)H(2)(+). The circular glow discharge source is easy to construct and deploy in proton transfer mass spectrometry studies at similar to 11 hPa. Continuous use of the system over time periods of many days and stable operation over time periods of months to years between disassembly and cleaning demonstrates its robustness. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:28 / 37
页数:10
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