化学
砷
氢化物
检出限
萃取(化学)
色谱法
质谱法
荧光光谱法
固相萃取
核化学
分析化学(期刊)
荧光
金属
有机化学
量子力学
物理
作者
Mariela N. Matos Reyes,M. Luisa Cervera,Reinaldo Campos‐Vargas,Miguel de la Guárdia
出处
期刊:Talanta
[Elsevier]
日期:2008-02-05
卷期号:75 (3): 811-816
被引量:44
标识
DOI:10.1016/j.talanta.2007.12.018
摘要
A non-chromatographic, sensitive and simple analytical method has been developed for the determination of toxic arsenic species in vegetable samples by hydride generation-atomic fluorescence spectrometry (HG-AFS). As(III), As(V), dimethylarsinic acid (DMA) and monomethylarsonic acid (MMA) were determined by hydride generation-atomic fluorescence spectrometry using a series of proportional equations. The method is based on a single extraction of the arsenic species considered from vegetables through sonication at room temperature with H3PO4 1 mol L−1 in the presence of 0.1% (w/v) Triton XT-114 and washing of the solid phase with 0.1% (w/v) EDTA, followed by direct measurement of the corresponding hydrides in four different experimental conditions. The limit of detection of the method was 3.1 ng g−1 for As(III), 3.0 ng g−1 for As(V), 1.5 ng g−1 for DMA and 1.9 ng g−1 for MMA, in all cases expressed in terms of sample dry weight. Recovery studies provided percentages greater than 91% for all considered species in spiked samples of chards and aubergines. Total toxic As found in the aforementioned samples was at the level of 90 ng g−1; As(III) is followed by As(V), DMA and MMA which are the main species of As in chards being As(V) the main As compound in aubergines.
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