Coupling corona discharge for ambient extractive ionization mass spectrometry

被引:12
作者
Hu, Bin [2 ]
Zhang, Xinglei [2 ]
Li, Ming [1 ]
Peng, Xuejiao [2 ]
Han, Jing [2 ]
Yang, Shuiping [2 ]
Ouyang, Yongzhong [2 ]
Chen, Huanwen [2 ]
机构
[1] Natl Inst Metrol, Beijing 100013, Peoples R China
[2] Coll Chem Biol & Mat Sci, E China Inst Technol, Jiangxi Key Lab Mass Spectrometry & Instrumentat, Nanchang 330013, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
DESORPTION ELECTROSPRAY-IONIZATION; LOW-TEMPERATURE PLASMA; ATMOSPHERIC-PRESSURE; CHEMICAL-IONIZATION; ION-SOURCE; TRACE ANALYSIS; IN-VIVO; BENZENE; PROBE; AIR;
D O I
10.1039/c1an15483d
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Unlike the extractive electrospray ionization (EESI) technique described elsewhere, a corona discharge instead of electrospray ionization has been utilized to charge a neutral solvent spray under ambient conditions for the generation of highly charged microdroplets, which impact a neutral sample plume for the extractive ionization of the analytes in raw samples without any sample pretreatment. Using the positive ion mode, molecular radical cations were easily generated for the detection of non-polar compounds (e.g., benzene, cyclohexane, etc.), while protonated molecular ions of polar compounds (e.g., acetonitrile, acetic ether) were readily produced for the detection. By dispensing the matrix in a relatively large space, this method tolerates highly complex matrices. For a given sample such as lily fragrances, more compounds were detected by the method established here than the EESI technique. An acceptable relative standard deviation (RSD 8.9%, n = 11) was obtained for the direct measurement of explosives (10 ppb) in waste water samples. The experimental data demonstrate that this method could simultaneously detect both polar and non-polar analytes with high sensitivity, showing promising applications for the rapid detection of a wide variety of compounds present in complex matrices.
引用
收藏
页码:4977 / 4985
页数:9
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