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采用氢化物发生技术与微漏斗辅助顶空液相微萃取相结合,用紫外可见分光光度法测定砷。

Hydride generation coupled to microfunnel-assisted headspace liquid-phase microextraction for the determination of arsenic with UV-Vis spectrophotometry.

机构信息

Department of Chemistry, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, Iran.

出版信息

Environ Monit Assess. 2014 Dec;186(12):8381-9. doi: 10.1007/s10661-014-4011-3. Epub 2014 Aug 27.

DOI:10.1007/s10661-014-4011-3
PMID:25154684
Abstract

In this research, a microfunnel-assisted headspace liquid-phase microextraction technique has been used in combination with hydride generation to determine arsenic (As) by UV-Vis spectrophotometry. The method is based on the reduction of As to arsine (AsH3) in acidic media by sodium tetrahydroborate (NaBH4) followed by its subsequent reaction with silver diethyldithiocarbamate (AgDDC) to give an absorbing complex at 510 nm. The complexing reagent (AgDDC) has been dissolved in a 1:1 (by the volume ratio) mixture of chloroform/chlorobenzene microdroplet and exposed to the generated gaseous arsine via a reversed microfunnel in the headspace of the sample solution. Several operating parameters affecting the performance of the method have been examined and optimized. Acetonitrile solvent has been added to the working samples as a sensitivity enhancement agent. Under the optimized operating conditions, the detection limit has been measured to be 0.2 ng mL(-1) (based on 3sb/m criterion, n b = 8), and the calibration curve was linear in the range of 0.5-12 ng mL(-1). The relative standard deviation for eight replicate measurements was 1.9 %. Also, the effects of several potential interferences have been studied. The accuracy of the method was validated through the analysis of JR-1 geological standard reference material. The method has been successfully applied for the determination of arsenic in raw and spiked soft drink and water samples with the recoveries that ranged from 91 to 106 %.

摘要

在这项研究中,采用了微漏斗辅助顶空液相微萃取技术,并结合氢化物发生法,通过紫外可见分光光度法测定砷(As)。该方法基于在酸性介质中,硼氢化钠(NaBH4)将 As 还原为胂(AsH3),随后与二乙基二硫代氨基甲酸银(AgDDC)反应,在 510nm 处生成吸收络合物。络合试剂(AgDDC)溶解在体积比为 1:1 的氯仿/氯苯微滴混合液中,并通过微漏斗的反向作用暴露于样品溶液顶空生成的气态胂中。研究了几种影响方法性能的操作参数,并对其进行了优化。在工作样品中加入乙腈溶剂作为增强灵敏度的试剂。在优化的操作条件下,检测限测量值为 0.2ng mL(-1)(基于 3sb/m 标准,n b = 8),校准曲线在 0.5-12ng mL(-1)范围内呈线性。八个重复测量的相对标准偏差为 1.9%。此外,还研究了几种潜在干扰的影响。通过对 JR-1 地质标准参考物质的分析验证了该方法的准确性。该方法已成功应用于测定原始和加标软饮料和水样中的砷,回收率范围为 91%至 106%。

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