Department of Chemistry, Faculty of Science, Srinakharinwirot University, Sukhumvit 23, Bangkok 10110, Thailand.
Flow Innovation-Research for Science and Technology Laboratories (Firstlabs), Thailand and Department of Chemistry, Center of the Excellence for Innovation in Chemistry, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Anal Methods. 2021 Jan 21;13(2):202-211. doi: 10.1039/d0ay01970d.
A new design of a membraneless vaporization (MBL-VP) unit coupled with a specific flow system is presented for the determination of arsenic at trace levels using a hydride generation process. The MBL-VP unit contains two concentric conical reservoirs, with the outer cone selected as the donor reservoir. The volume of the outer donor reservoir is thereby greater than the acceptor volume, necessary for holding sufficient sample and reagents for the generation of arsine gas by reaction between As(iii) and sodium borohydride under acidic conditions. The arsine gas diffuses into the narrow headspace and is absorbed by an aliquot of 150 μL of mercuric chloride acceptor solution. The resulting reaction produces hydronium ions which is monitored by the absorbance change at 530 nm of the methyl orange indicator added in the acceptor solution. To decrease the detection limit, the aspiration and removal of the donor plug, comprising the sample, borohydride and acid, into and out of the donor cone are repeated several times, while the acceptor solution is kept unchanged. As a result, analysis of arsenic was achieved in the range of 10 to 100 μg L-1 with a detection limit of 8 μg L-1. Application to surface water was investigated. Percent recoveries of spiked surface water samples were in the range of 94-110%. For comparison of total arsenic (As(iii) and As(v)), the results obtained from the developed method are not statistically different from the ICP-OES method.
提出了一种新的无膜蒸发(MBL-VP)单元设计,该设计与特定的流动系统相结合,用于使用氢化物发生法测定痕量砷。MBL-VP 单元包含两个同心圆锥形储液器,其中外锥用作供体储液器。外供体储液器的体积大于接受器的体积,这对于在酸性条件下使 As(III)与硼氢化钠反应生成胂气,从而容纳足够的样品和试剂是必需的。胂气扩散到狭窄的顶空部分,并被 150 μL 的氯化汞接受溶液的一部分吸收。生成的反应产生氢离子,通过加入到接受溶液中的甲基橙指示剂在 530nm 处的吸光度变化来监测。为了降低检测限,将包含样品、硼氢化钠和酸的供体塞子吸入和移出供体锥,重复几次,而接受溶液保持不变。因此,砷的分析范围为 10 至 100μg L-1,检测限为 8μg L-1。对地表水进行了应用研究。加标地表水样品的回收率在 94-110%之间。对于总砷(As(III)和 As(v))的比较,开发方法得到的结果与 ICP-OES 方法没有统计学差异。