Characterization of a Membrane Interface for Analysis of Air Samples Using Time-of-flight Mass Spectrometry

被引:2
作者
Jang, Yu-Mi [1 ,2 ]
Oh, Jun-Sik [1 ,2 ]
Park, Chang Joon [3 ]
Yang, Sang Sik [4 ]
Jung, Kwang-Woo [1 ,2 ]
机构
[1] Wonkwang Univ, Dept Chem, Iksan 570749, Chonbuk, South Korea
[2] Wonkwang Univ, Inst Nanosci & Tech, Iksan 570749, Chonbuk, South Korea
[3] Korea Res Inst Stand & Sci, Taejon 305340, South Korea
[4] Ajou Univ, Div Elect & Comp Engn, Suwon 443749, South Korea
关键词
Membrane inlet; Polydimethylsiloxane (PDMS); Time-of-flight mass spectrometry; Diffusion coefficient; VOLATILE ORGANIC-COMPOUNDS; INLET; PERMEATION; WATER; TRAP; PROBE;
D O I
10.5012/bkcs.2010.31.10.2791
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the present study, we constructed a membrane inlet assembly for selective permeation of volatile airborne organic compounds for subsequent analysis by time-of-flight mass spectrometry. The time-dependent diffusion of analytes through a 75 mu m thick polydimethylsiloxane membrane was measured by monitoring the ion signal after a step change in the sample concentration. The results fit well to a non-steady-state permeation equation. The diffusion coefficient, response time, and sensitivity were determined experimentally for a range of polar (halogenated) and nonpolar (aromatic) compounds. We found that the response times for several volatile organic compounds were greatly influenced by the alkyl chain length as well as the size of the substituted halogen atoms. The detection limits for benzene, ethylbenzene, and 2-propanol were 0.2 ppm, 0.1 ppm, and 3.0 ppm by volume, respectively, with a linear dynamic range greater than three orders of magnitude. These results indicate that the membrane inlet/time-of-flight mass spectrometry technique will be useful for a wide range of applications, particularly for in situ environmental monitoring.
引用
收藏
页码:2791 / 2796
页数:6
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