使用电感耦合等离子体串联质谱法观测气体纯度对与 NO 反应性的影响

IF 3.6 3区 化学 Q2 CHEMISTRY, ANALYTICAL Analyst Pub Date : 2024-10-16 DOI:10.1039/d4an01227e
Amanda French, Kirby P Hobbs, Richard M Cox, Isaac J Arnquist
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The impact of gas purity on observed reactivity with NO using inductively coupled plasma tandem mass spectrometry
Interference removal in inductively coupled plasma tandem mass spectrometry (ICP-MS/MS) is strongly dependent on the gas selected for use within the collision/reaction cell. There has been little investigation on the effects that reaction gas impurities may have on the resulting spectra. The reactivity of 60 elements was evaluated using nitric oxide (NO 99.5%) with and without a gas purifier to reduce H2O impurities to < 100 pptV. Experiments were performed using V, Ce, Tl and Th to investigate the effects of purified NO at various flowrates (0.22 – 1.49 mL min-1). Purified NO was shown to significantly mitigate oxy-hydride interferences, improve total ion sensitivity (notable at high gas flows), and shift product distributions advantageously. The reduction in oxy-hydride species results in a product distribution favoring the major expected products, where signals were shown to increase by an order of magnitude. Reduced background and increased signal for the major expected products provides avenues for improving various analytical applications of ICP-MS/MS.
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来源期刊
Analyst
Analyst 化学-分析化学
CiteScore
7.80
自引率
4.80%
发文量
636
审稿时长
1.9 months
期刊介绍: The home of premier fundamental discoveries, inventions and applications in the analytical and bioanalytical sciences
期刊最新文献
Designing a Novel Paper-based Microfluidic Disc for rapid and Simultaneous Determination of Multiple Nutrient Salts in Water. Surface-enhanced Raman spectroscopy with single cell manipulation by microfluidic dielectrophoresis The impact of gas purity on observed reactivity with NO using inductively coupled plasma tandem mass spectrometry Imaging specific proteins in living cells with small unnatural amino acid attached Raman reporters Probing the role of ligation and exonuclease digestion towards non-specific amplification in bioanalytical RCA assays
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