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Determination of trace arsenic(III), arsenic(V), antimony(III), antimony(V) in drain by ICP equipped with hydridegeneration system

机译:通过ICP配备有氢化物再生系统的痕量砷(III),砷(V),锑(III),锑(V),锑(V)

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By newly developed ICP method, trace amounts of As(III), As(V) ,Sb(III) arid Sb(V) were precisely determined within accuracy of sub ng/ml. As(III) and Sb(III) were separated from As(V) and Sb(V) by extracting into Xylene as diethyldithiocarbamate complexes using diethylammonium diethyldithiocarbamate (DDDC), and then back-extracted into nitric acid for a quantitative determination by ICP-AES equipped with hydridegeneration system. The recoveries of As(III) and Sb(III) were satisfactory throughout the extraction with 0.04mol/l DDDC in xylene from 1mol/l hydrochloric acid solution and the back-extraction with 7 mol/l nitric acid. As(V) and Sb(V) were reduced to As(III) arid Sb(III) by ascorbic acid and potassium iodide, and their quantities were determined as mentioned above. The detection limits were found to be 0.58ng/ml for As(III), 0.63ng/ml for Sb(III) using 50ml of a sample. The proposed method was applied to analysis of the real sample.
机译:通过新开发的ICP方法,将痕量为(III),AS(v),Sb(III)干旱Sb(v)在亚Ng / ml的准确性内。作为(iii)和Sb(III)通过用二乙基二硫代氨基甲酸二甲磺酸酯(DDDC)作为二乙基二硫代氨基甲酸酯复合物萃取到二甲苯酯中,然后通过ICP萃取到硝酸中的硝酸中的硝酸 - AES配备了Hydide Generation系统。作为(III)和Sb(III)的回收率在整个萃取过程中令人满意,在1mol / L盐酸溶液中的0.04mol / L DDDC中用0.04mol / L DDDC和7mol / L硝酸的后萃取。作为(v)和Sb(v)通过抗坏血酸和碘化钾还原为(iii)干旱的Sb(III),并如上所述测定它们的量。使用50ml样品,发现检测限为0.58ng / ml,对于Sb(III),对于Sb(III),0.63ng / ml。所提出的方法应用于实际样品的分析。

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