Direct aqueous injection analysis of trace compounds in water with proton-transfer-reaction mass spectrometry (PTR-MS)

被引:10
|
作者
Juerschik, S. [2 ]
Tani, A. [3 ]
Sulzer, P. [2 ]
Haidacher, S. [2 ]
Jordan, A. [2 ]
Schottkowsky, R. [2 ]
Hartungen, E. [2 ]
Hanel, G. [2 ]
Seehauser, H. [2 ]
Maerk, L. [2 ]
Maerk, T. D. [1 ,2 ]
机构
[1] Leopold Franzens Univ Innsbruck, Inst Ionenphys & Angew Phys, A-6020 Innsbruck, Austria
[2] Ion Analyt Gesell mbH, A-6020 Innsbruck, Austria
[3] Osaka Univ, Grad Sch Sci, Dept Earth & Space Sci, Osaka 5600043, Japan
关键词
PTR-MS; Water analysis; Proton-transfer-reaction; Direct injection; Online quantification;
D O I
10.1016/j.ijms.2009.11.002
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
Here we present proof-of-principle investigations on a novel inlet system for proton-transfer-reaction mass spectrometry (PTR-MS) that allows for the analysis of trace compounds dissolved in water. The PTR-MS technique offers many advantages, such as real-time analysis, online quantification, no need for sample preparation, very low detection limits, etc.; however it requires gas phase samples and therefore liquid samples cannot be investigated directly. Attempts to measure trace compounds in water that have been made so far are mainly headspace analysis above the water surface and membrane inlet setups, which both are well suitable for certain applications, but also suffer from significant disadvantages. The direct aqueous injection(DAI) technique which we will discuss here turns out to be an ideal solution for the analysis of liquid samples with PTR-MS. We show that we can detect trace compounds in water over several orders of magnitude down to a concentration level of about 100 pptw, while only consuming about 100 mu l of the sample. The response time of the setup is about 20s and can therefore definitely be called "online". Moreover the method is applicable to the analysis of all substances and not limited by the permeability of a membrane. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:173 / 176
页数:4
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