Determination of Vanadium (IV) and (V) in Southern Nevada Groundwater by Ion Chromatography-Inductively Coupled Plasma Mass Spectrometry

Sujanie Gamage, V. Hodge, J. Cizdziel, Kazumasa Lindley
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引用次数: 14

Abstract

A rapid method is presented for measuring V(IV) and V(V) in groundwater, without preconcentration or complexing agents, using direct injection of the water samples (which were collected under an argon atmosphere) into an ion chromatograph-inductively coupled plasma mass spectrometer (ICPMS). The mobile phase is 1.5% v/v nitric acid, which minimizes the buildup of solids in the ultrasonic nebulizer, the torch, and on the entrance cones of the ICPMS - a problem with methods using organic complexing agents and inorganic salts. The result is much less instrument downtime for cleaning the affected parts. Limits of detection are 0.02 � g L -1 for V(IV) and 0.06 � g L -1 for V(V). The pentavalent form of vanadium represents 98% to 99% of the vanadium in these Southern Nevada groundwater samples and ranges from 3.7±0.1 � g L -1 to 82.1±0.5 � g L -1 . The remaining few percent is V(IV). Total vanadium was determined by ICPMS
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离子色谱-电感耦合等离子体质谱法测定内华达州南部地下水中的钒(IV)和(V)
本文提出了一种不用预浓缩和络合剂,直接将氩气环境下采集的水样注入离子色谱-电感耦合等离子体质谱仪(ICPMS)中,快速测定地下水中V(IV)和V(V)的方法。流动相是1.5% v/v的硝酸,这可以最大限度地减少超声波雾化器、火炬和ICPMS入口锥上固体的堆积,这是使用有机络合剂和无机盐的方法的一个问题。其结果是更少的仪器停机时间清洗受影响的部分。V(IV)的检测限为0.02 μ g L -1, V(V)的检测限为0.06 μ g L -1。在这些南内华达州地下水样品中,钒的五价形态占98%至99%,范围从3.7±0.1 μ g L -1到82.1±0.5 μ g L -1。剩下的几个百分比是V(IV)。用ICPMS法测定总钒
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