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利用选择性氢化物发生法实现无需色谱分离的物种鉴定:稻米和海洋源样品中的无机砷。

Speciation without chromatography using selective hydride generation: inorganic arsenic in rice and samples of marine origin.

机构信息

TESLA-Trace Element Speciation Laboratory, Department of Chemistry, University of Aberdeen , Aberdeen, AB24 3UE, Scotland, U.K.

出版信息

Anal Chem. 2014 Jan 21;86(2):993-9. doi: 10.1021/ac403438c. Epub 2014 Jan 9.

Abstract

Because of the toxicity of inorganic arsenic (iAs), only iAs needs to be monitored in food and feedstuff. This demands the development of easy and quick analytical methods to screen large number of samples. This work focuses on hydride generation (HG) coupled with an ICPMS as an arsenic detector where the HG is added as a selective step to determine iAs in the gaseous phase while organically bound As remains in the solution. iAs forms volatile arsine species with high efficiency when treated with NaBH4 at acidic conditions, whereas most other organoarsenic compounds do not form any or only less volatile arsines. Additionally, using high concentrations of HCl further reduces the production of the less volatile arsines and iAs is almost exclusively formed, therefore enabling to measure iAs without a prior step of species separation using chromatography. Here, we coupled a commercially available HG system to an ICPMS and optimized for determination of iAs in rice and samples of marine origin using different acid concentrations, wet and dry plasma conditions, and different reaction gas modes. Comparing this method to conventional HPLC-ICPMS, no statistical difference in iAs concentration was found and comparable limits of detections were achieved using less than half the instrument time.

摘要

由于无机砷(iAs)的毒性,食品和饲料中仅需监测 iAs。这就需要开发简单快速的分析方法来筛选大量的样品。本工作专注于氢化物发生(HG)与 ICPMS 相结合作为砷检测器,其中 HG 作为选择性步骤添加,以在气相中测定 iAs,而有机结合的 As 则保留在溶液中。在酸性条件下用 NaBH4 处理时,iAs 与硼氢化钠高效地形成挥发性胂化物,而大多数其他有机砷化合物则不形成任何或仅形成较少挥发性的胂化物。此外,使用高浓度的 HCl 进一步减少了较少挥发性的胂化物的生成,几乎仅形成 iAs,因此能够在不使用色谱法进行物种分离的情况下直接测量 iAs。在这里,我们将一种市售的 HG 系统与 ICPMS 耦合,并针对使用不同酸浓度、湿等离子体和干等离子体条件以及不同反应气体模式的大米和海洋来源样品中的 iAs 进行了优化。与传统的 HPLC-ICPMS 相比,该方法未发现 iAs 浓度存在统计学差异,并且使用不到一半的仪器时间即可实现可比的检测限。

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