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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Determination of total chrominum in tannery waste water by inductively coupled plasma-atomic emission spectometry,flame atomic absorption spectrometry and UV-visible spectrophotometric methods
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Determination of total chrominum in tannery waste water by inductively coupled plasma-atomic emission spectometry,flame atomic absorption spectrometry and UV-visible spectrophotometric methods

机译:电感耦合等离子体原子发射光谱法,火焰原子吸收光谱法和紫外可见分光光度法测定制革废水中的总铬

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摘要

The determination of total chromium in different in different streams of tannery effluents were carried out by the digestion of samples in a HNO_3/H_2SO_4 imxture followed by KMnO_4 oxidation,which resulted in the complete conversion of Cr(III)to Cr(VI).The Cr(VI)(Cr-2O_7~2-)species present in these samples were estimated by inductively coupled plasma-atomic emission spectrometry (ICP-AES),flame atomic absorption spectrometry (FAAS)and UV-visible spectrophotometry (1,5-diphenyl carbazide method).The results obtained from these methods were critically evaluated.UV-visible spectrophotometry was found to be better suited for this anlaysis when compared with the other two methods.Since these solutions contain relatively high concentrations of chromium (200-2400 mg/l),the need for preconcentration did not arise.The higher values ogbtained in the case of ICP-AES and FAAS methods can be attributed to the matrix effect arising out of high concentration of mineral acids and electrolytes.In addition,the values obtained in the latter methods (ICP-AES and FAAS)are comparable with each other,indicating that the interferences influenece the results almost equally in both techniques.The statistical treatment of data indicates that the differences between the methods are within the acceptable range.
机译:通过在HNO_3 / H_2SO_4混合液中消解样品,然后进行KMnO_4氧化,从而完成Cr(III)到Cr(VI)的完全转化,从而测定了不同制革厂废水流中总铬的含量。通过电感耦合等离子体原子发射光谱法(ICP-AES),火焰原子吸收光谱法(FAAS)和紫外可见分光光度法(1,5-)估算了这些样品中的Cr(VI)(Cr-2O_7〜2-)种类。严格评估了从这些方法获得的结果。与其他两种方法相比,紫外可见分光光度法被发现更适合于该分析法,因为这些溶液中铬的浓度相对较高(200-2400 mg / l),不需要进行预浓缩。ICP-AES和FAAS方法获得的较高值可以归因于高浓度的无机酸和电解质引起的基质效应。因此,后一种方法(ICP-AES和FAAS)获得的值彼此可比,表明两种方法中干扰对结果的影响几乎相等。对数据的统计处理表明,这两种方法之间的差异在可接受范围。

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