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Non-Extractive Quenchophotometric Method for Determination of Trace Arsenic in Alloys, Environmental Waters, Biological and Soil Samples

机译:非萃取萃取光度法测定合金,环境水,生物和土壤样品中的痕量砷

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摘要

A simple, non-extractive, highly sensitive and selective quenchophotometric method for the rapid determination of arsenic at trace levels in aqueous medium has been developed. The method is based on the oxidation of arsenic (III) by potassium bromate in the presence of potassium bromide and methyl orange. The decrease in native absorbance of the reagent blank ( λ_(max) = 393 nm) was inversely proportional to the amount of arsenic in aqueous solution. The absorbance quenching due to arsenic (III) is achieved by subtracting the relative absorbance of arsenic-reagent system from that of the corresponding reagent blank system. The reaction is instantaneous and the absorbance remains stable for over 24h. The absorbance vs arsenic (III) concentration calibration graph shows a rectilinear relationship for a wide range 1-250 μg mL~(-1) of As (III). Large amount of about 50 cations, anions and complexing agents do not interfere in the determination. The method was successfully used for the determination of arsenic in several standard reference materials (alloys and steels) as well as in some environmental waters (underground and surface), biological samples (human blood, urine, hair and nails) and soil samples. Solution containing both arsenic (III) and arsenic (V) and complex synthetic mixtures were also successfully analysed using the proposed method. The method has high precision and accuracy (s = ±0.01 for 5 μξ mL~(-1)) of analyte.
机译:开发了一种简单,非萃取,高灵敏度和选择性的测光光度法,用于快速测定水性介质中的痕量砷。该方法基于在溴化钾和甲基橙的存在下,溴酸钾将砷(III)氧化。试剂空白的天然吸光度降低(λ_(max)= 393 nm)与水溶液中的砷含量成反比。通过从相应试剂空白系统的相对吸光度中减去砷试剂系统的相对吸光度,可以实现由于砷(III)引起的吸光度猝灭。反应是瞬时的,吸光度保持稳定超过24小时。吸光度与砷(III)浓度的校准曲线显示了在1-250μgmL〜(-1)的As(III)的宽范围内的直线关系。大量的约50种阳离子,阴离子和络合剂不会干扰测定。该方法已成功用于多种标准参考材料(合金和钢)以及某些环境水(地下和地表),生物样品(人血,尿液,头发和指甲)和土壤样品中砷的测定。使用建议的方法还成功地分析了同时含有砷(III)和砷(V)的溶液以及复杂的合成混合物。该方法具有较高的分析精度和准确性(5μξmL〜(-1)时s =±0.01)。

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