Characterization of arsenic species by liquid sampling-atmospheric pressure glow discharge ionization mass spectrometry

被引:2
作者
Goodwin, Joseph [1 ]
Marcus, R. Kenneth [1 ]
McRae, Garnet [2 ]
Sturgeon, Ralph E. [2 ]
Mester, Zoltan [2 ]
机构
[1] Clemson Univ, Dept Chem, Clemson, SC 29634 USA
[2] Metrol Res Ctr, Natl Res Council Canada, Ottawa, ON K1A0R6, Canada
关键词
Speciation; Glow discharge; Arsenic; Mass spectrometry; APGD; ELECTROSPRAY-IONIZATION; ICP-MS; DESORPTION-IONIZATION; GAS-CHROMATOGRAPHY; REAL-TIME; SPECIATION; IDENTIFICATION;
D O I
10.1007/s00216-024-05312-x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A liquid sampling-atmospheric pressure glow discharge (LS-APGD) ionization source operating at a nominal power of 30 W and solution flow rate of 30 mu L min-1 and supported in a He sheath gas flow rate of 500 mL min-1 was interfaced to an Orbitrap mass spectrometer and assessed for use in rapid identification of inorganic and organic arsenic species, including As(III), As(V), monomethylarsonic acid, dimethylarsinic acid, and arsenobetaine in a 2% (v/v) nitric acid medium. Mass spectral acquisition in low-resolution mode, using only the ion trap analyzer, provided detection of protonated molecular ions for AsBet (m/z 179), DMA (m/z 139), MMA (m/z 141), and As(V) (m/z 143). As(III) is oxidized to As(V), likely due to in-source processes. Typical fragmentation of these compounds resulted in the loss of either water or methyl groups, as appropriate, i.e., introducing DMA also generated ions corresponding to MMA and As(V) as dissociation products. Structure assignments were also confirmed by high-resolution Orbitrap measurements. Spectral fingerprint assignments were based on the introduction of solutions containing 5 mu g mL-1 of each arsenic compound.
引用
收藏
页码:3585 / 3594
页数:10
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