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首页> 外文期刊>International journal of environmental analytical chemistry >Determination of arsenic(III) and total inorganic arsenic in water samples using variable tetrahydroborate(III) and acid concentrations by continuous-flow hydride-generation atomic absorption spectrometry
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Determination of arsenic(III) and total inorganic arsenic in water samples using variable tetrahydroborate(III) and acid concentrations by continuous-flow hydride-generation atomic absorption spectrometry

机译:连续氢化物发生原子吸收光谱法使用可变的四氢硼酸根和酸浓度测定水样中的砷和总无机砷

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摘要

A simple procedure was developed for the direct determination of As(III) and total inorganic arsenic in water samples using continuous-flow hydride generation atomic absorption spectrometry without prereduction of As(V). Under optimized conditions, As(III) was determined using 1% w/v of NaBH_4 and 0.2 mol L~(-1) of HC1, and total arsenic using 5% w/v of NaBH_4 and 6 mol L~(-1) of HCl. The concentration of As(V) was determined by the difference between total inorganic arsenic and concentration of As(III). Interferences from methylated arsenic species, mutual hydride-forming, and transition elements in the determination of As(III) and total arsenic were evaluated. With the proposed procedure, detection limits of 0.1 μg L~(-1) for As(III) and 0.25 μg L~(-1) for total arsenic were achieved. The relative standard deviations were 2.0% for 2 μg L~(-1) of As(III) and 3.5% for 2 μg L~(-1) of As(V) determined as total arsenic. Spike recoveries were in the range of 91-111% for As(III) and 91-114% for As(V). The method was validated by analysing certified reference materials SRM-1640 and NASS-5. The developed methodology constitutes an economic, simple, and reliable way to determine inorganic arsenic species in natural waters and other similar samples with negligible or no content of methylated arsenic species. Speciation analysis was satisfactorily applied to different types of natural water samples.
机译:开发了一种简单的程序,使用连续氢化物发生原子吸收光谱法无需预先还原As(V),即可直接测定水中的As(III)和总无机砷。在优化的条件下,使用1%w / v的NaBH_4和0.2 mol L〜(-1)的HCl测定As(III),使用5%w / v的NaBH_4和6 mol L〜(-1)的测定总砷盐酸。 As(V)的浓度由总无机砷和As(III)的浓度之差确定。在确定As(III)和总砷的过程中,评估了甲基化砷物种,相互氢化物形成和过渡元素的干扰。通过所提出的方法,砷(III)的检出限为0.1μgL〜(-1),总砷的检出限为0.25μgL〜(-1)。测定为总砷的2μgL〜(-1)的相对标准偏差为2.0%,而砷(V)的2μgL〜(-1)的相对标准偏差为3.5%。 As(III)的加标回收率在91-111%范围内,As(V)的加标回收率在91-114%范围内。该方法通过分析认证参考材料SRM-1640和NASS-5进行了验证。所开发的方法论是一种经济,简单和可靠的方法,可用于测定天然水和其他类似样品中的甲基化砷物种含量可忽略不计或不存在的无机砷物种。形态分析令人满意地应用于不同类型的天然水样品。

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