Atmospheric-pressure solution-cathode glow discharge: A versatile ion source for atomic and molecular mass spectrometry

被引:41
|
作者
Schwartz, Andrew J. [1 ]
Williams, Kelsey L. [2 ]
Hieftje, Gary M. [1 ]
Shelley, Jacob T. [2 ,3 ]
机构
[1] Indiana Univ, Dept Chem, Bloomington, IN 47405 USA
[2] Kent State Univ, Dept Chem & Biochem, Kent, OH 44242 USA
[3] Rensselaer Polytech Inst, Dept Chem & Chem Biol, 110 8th St, Troy, NY 12180 USA
关键词
Solution-cathode glow discharge; Mass spectrometry; Ionization source development; Elemental analysis; Ambient desorption/ionization; Tunable fragmentation; APGD IONIZATION SOURCE; EMISSION-SPECTROMETRY; DESORPTION-IONIZATION; ELEMENTAL ANALYSIS; OPTICAL-EMISSION; AQUEOUS SAMPLES; OPEN-AIR; WATER; COMPACT; ACETATE;
D O I
10.1016/j.aca.2016.10.045
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An atmospheric-pressure solution-cathode glow discharge (SCGD) has been evaluated as an ion source for atomic, molecular, and ambient desorption/ionization mass spectrometry. The SCGD consists of a direct-current plasma, supported in the ambient air in the absence of gas flows, and sustained upon the surface of a flowing liquid cathode. Analytes introduced in the flowing liquid, as an ambient gas, or as a solid held near the plasma are vaporized and ionized by interactions within or near the discharge. Introduction of acidic solutions containing metal salts produced bare elemental ions as well as H2O, OH- and NO3- adducts. Detection limits for these elemental species ranged from 0.1 to 4 ppb, working curves spanned more than 4 orders of linear dynamic range, and precision varied between 5 and 16% relative standard deviation. Small organic molecules were also efficiently ionized from solution, and both the intact molecular ion and fragments were observed in the resulting SCGD mass spectra. Fragmentation of molecular species was found to be tunable; high discharge currents led to harder ionization, while low discharge currents produced stronger molecular-ion signals. Ambient gases and solids, desorbed by the plasma from a glass probe, were also readily ionized by the SCGD. Indeed, strong analyte signals were obtained from solid samples placed at least 2 cm from the plasma. These findings indicate that the SCGD might be useful also for ambient desorption/ionization mass spectrometry. Combined with earlier results that showed the SCGD is useful for ionization of labile biomolecules, the results here indicate that the SCGD is a highly versatile ion source capable of providing both elemental and molecular mass-spectral information. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:119 / 128
页数:10
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