Direct Detection of Benzene, Toluene, and Ethylbenzene at Trace Levels in Ambient Air by Atmospheric Pressure Chemical Ionization Using a Handheld Mass Spectrometer

被引:78
|
作者
Huang, Guangming [1 ,2 ]
Gao, Liang [1 ,2 ]
Duncan, Jason [1 ,2 ]
Harper, Jason D. [1 ,2 ]
Sanders, Nathaniel L. [1 ,2 ]
Ouyang, Zheng [3 ]
Cooks, R. Graham [1 ,2 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
[2] Purdue Univ, Ctr Analyt Instrumentat Dev, W Lafayette, IN 47907 USA
[3] Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
关键词
SOLID-PHASE MICROEXTRACTION; VOLATILE ORGANIC-COMPOUNDS; ON-SITE DETECTION; WARFARE AGENTS; MEMBRANE INLET; QUANTITATIVE-ANALYSIS; DETECTION SYSTEM; TOXIC COMPOUNDS; SAMPLE VOLUME; GASOLINE;
D O I
10.1016/j.jasms.2009.09.018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The capabilities of a portable mass spectrometer for real-time monitoring of trace levels of benzene, toluene, and ethylbenzene in air are illustrated. An atmospheric pressure interface was built to implement atmospheric pressure chemical ionization for direct analysis of gas-phase samples on a previously described miniature mass spectrometer (Gao et al. Anal. Chem. 2006, 78, 5994-6002). Linear dynamic ranges, limits of detection and other analytical figures of merit were evaluated: for benzene, a limit of detection of 0.2 parts-per-billion was achieved for air samples without any sample preconcentration. The corresponding limits of detection for toluene and ethylbenzene were 0.5 parts-per-billion and 0.7 parts-per-billion, respectively. These detection limits are well below the compounds' permissible exposure levels, even in the presence of added complex mixtures of organics at levels exceeding the parts-per-million level. The linear dynamic ranges of benzene, toluene, and ethylbenzene are limited to approximately two orders of magnitude by saturation of the detection electronics. (J Am Soc Mass Spectrom 2010, 21, 132-135) (C) 2010 American Society for Mass Spectrometry
引用
收藏
页码:132 / 135
页数:4
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