Humidity independent mass spectrometry for gas phase chemical analysis via ambient proton transfer reaction

被引:0
|
作者
Zhu, Hongying [1 ]
Huang, Guangming [1 ]
机构
[1] Univ Sci & Technol China, Dept Chem, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Mass spectrometry; Ambient proton transfer reaction; Gas phase sample analysis; Humidity independent; Ultrasonic spray; VOLATILE ORGANIC-COMPOUNDS; THERMAL-DESORPTION; GASTROESOPHAGEAL CANCER; SENSOR ARRAY; MS ANALYSIS; BREATH; IONIZATION; AIR; TIME; SAMPLING/IONIZATION;
D O I
10.1016/j.aca.2015.02.043
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, a humidity independent mass spectrometric method was developed for rapid analysis of gas phase chemicals. This method is based upon ambient proton transfer reaction between gas phase chemicals and charged water droplets, in a reaction chamber with nearly saturate humidity under atmospheric pressure. The humidity independent nature enables direct and rapid analysis of raw gas phase samples, avoiding time-and sample-consuming sample pretreatments in conventional mass spectrometry methods to control sample humidity. Acetone, benzene, toluene, ethylbenzene and metaxylene were used to evaluate the analytical performance of present method. The limits of detection for benzene, toluene, ethylbenzene and meta-xylene are in the range of similar to 0.1 to similar to 0.3 ppbV; that of benzene is well below the present European Union permissible exposure limit for benzene vapor (5 mu g m(-3), similar to 1.44 ppbV), with linear ranges of approximately two orders of magnitude. The majority of the homemade device contains a stainless steel tube as reaction chamber and an ultrasonic humidifier as the source of charged water droplets, which makes this cheap device easy to assemble and facile to operate. In addition, potential application of this method was illustrated by the real time identification of raw gas phase chemicals released from plants at different physiological stages. (c) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:67 / 73
页数:7
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