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首页> 外文期刊>Analytical chemistry >Hydride generation interface for speciation analysis coupling capillary electrophoresis to inductively coupled plasma mass spectrometry
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Hydride generation interface for speciation analysis coupling capillary electrophoresis to inductively coupled plasma mass spectrometry

机译:氢化物发生界面,用于形态分析,毛细管电泳与电感耦合等离子体质谱的耦合

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摘要

A novel hydride generation (HG) interface for coupling capillary electrophoresis (CE) with inductively coupled plasma mass spectrometry (ICPMS) is presented in this work. The CE-HG-ICPMS interface was applied to the separation and quantitation of common arsenic species. Lack of a commercially available HG interface for CE-ICPMS led to a three concentric tube design allowing alleviation of back pressure commonly observed in CE-HG-ICPMS. Due to the high sensitivity and element-specific detection of ICPMS, quantitative analysis of As(III), As(V), monomethylarsonic acid, and dimethylarsinic acid was achieved. Optimization of CE separation conditions resulted in the use of 20 mmol L-1 sodium borate with 2% osmotic flow modifier (pH 9.0) and -20 kV applied potential for baseline resolution of each arsenic species in the shortest time. Hydride generation conditions were optimized through multiple electrophoretic separation analyses with 5% HCl and 3% NaBH4 (in 0.2% NaOH) determined to be the optimum conditions. After completion of system optimization, detection limits obtained for the arsenic species were less than 40 ng L-1 with electromigration time precision less than 1% within a total analysis time of 9.0 min. Finally, the interface was used for speciation analysis of arsenic in river and tap water samples.
机译:在这项工作中提出了一种新型的氢化物发生(HG)界面,用于将毛细管电泳(CE)与电感耦合等离子体质谱(ICPMS)耦合。 CE-HG-ICPMS接口用于常见砷物质的分离和定量。 CE-ICPMS缺少可购买的HG接口,导致了三个同心管设计,从而减轻了CE-HG-ICPMS中常见的背压。由于ICPMS的高灵敏度和特定元素的检测,实现了对As(III),As(V),单甲基砷酸和二甲基砷酸的定量分析。通过优化CE分离条件,可以在最短的时间内使用20 mmol L-1硼酸钠和2%渗透流量调节剂(pH 9.0)和-20 kV施加电势对每种砷进行基线分离。通过多次电泳分离分析对氢化物的生成条件进行了优化,其中5%HCl和3%NaBH4(在0.2%NaOH中)被确定为最佳条件。系统优化完成后,在9.0分钟的总分析时间内,砷的检出限小于40 ng L-1,电迁移时间精度小于1%。最后,该界面用于河流和自来水样品中砷的形态分析。

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