Characterization of Direct-Current Atmospheric-Pressure Discharges Useful for Ambient Desorption/Ionization Mass Spectrometry

被引:114
作者
Shelley, Jacob T. [1 ]
Wiley, Joshua S. [1 ]
Chan, George C. Y. [1 ]
Schilling, Gregory D. [1 ]
Ray, Steven J. [1 ]
Hieftje, Gary M. [1 ]
机构
[1] Indiana Univ, Dept Chem, Bloomington, IN 47405 USA
关键词
CHEMICAL-IONIZATION SOURCE; GLOW-DISCHARGE; DESORPTION-IONIZATION; ORGANIC-COMPOUNDS; ION-SOURCE;
D O I
10.1016/j.jasms.2008.12.020
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Two relatively new ambient ionization source, direct analysis in real time (DART) and the flowing atmospheric-pressure afterglow (FAPA), Use direct current, atmospheric-pressure discharges to produce reagent ions for the direct ionization of a sample. Although at a first glance these two sources appear similar, a fundamental study reveals otherwise. Specifically, DART was found to operate with a corona-to-glow, transition (C-G) discharge whereas the FAPA was found to operate with a glow-to-arc transition (G-A) discharge. The characteristics of both discharges were evaluated on the basis Of four factors: reagent-ion production, response to a model analyte (ferrocene), infrared (IR) thermography of the gas used for desorption and ionization, and spatial emission characteristics. The G-A discharge produced a greater abundance and a wider variety of reagent ions than the C-G discharge. In addition, the discharges yielded different adducts and signal strengths for ferrocene. It was also found that the gas exiting the discharge chamber reached a maximum of 235 degrees C and 55 degrees C for the G-A and C-G discharges, respectively. Finally, spatially resolved emission maps of both discharges showed clear differences for N-2(+) and O(I). These findings demonstrate that the discharges Used by FAPA and DART are fundamentally different and should have different optimal applications for ambient desorption/ionization mass spectrometry (ADI-MS). (J Am Soc Mass Spectrom 2009, 20, 837-844) (C) 2009 Published by Elsevier Inc. on behalf of American Society for Mass Spectrometry
引用
收藏
页码:837 / 844
页数:8
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