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Voltammetric Studies and Determination of Antimony(III)

机译:伏安法研究和测定锑(III)

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摘要

A detailed voltammetric study of Sb(III) has resulted in optimization of analytical conditions for determination of antimony at low concentration of submicrogram level by using differential pulse polarographic method. Among different supporting electrolytes investigated for the study of Sb(III), 0.8 M glycolic acid-ammonia was found most adequate where a well-defined wave was obtained at -0.30 V for the electroreduction of Sb(III) to Sb(0). It was observed that on increasing the concentration of Sb( III) the peak current increased linearly up to a concentration of 30 ppm. Limit of determination was observed to be 0.01 μg/mL. Cu(II), Pb(II), Cd(II), As(III) and Zn(II) did not interfere. The differential pulse polarography determination of antimony(III) was evaluated for its accuracy and precision in terms of standard deviation and percentage error. The method has been successfully applied for analysis of antimony in industrial waste samples and atomic absorption spectrophotometer method was used to compare the results obtained by differential pulse polarography.
机译:对Sb(III)的详细伏安研究已优化了使用微分脉冲极谱法测定亚微米级低浓度锑的分析条件。在研究用于Sb(III)研究的不同支持电解质中,发现0.8 M的乙醇酸-氨最合适,其中在-0.30 V处获得了清晰可见的波,可以将Sb(III)电还原为Sb(0)。观察到,随着Sb(III)浓度的增加,峰值电流线性增加,直至30 ppm的浓度。观察到的测定极限为0.01μg/ mL。 Cu(II),Pb(II),Cd(II),As(III)和Zn(II)没有干扰。根据标准偏差和百分误差,对差分脉冲极谱法测定锑(III)的准确性和精密度进行了评估。该方法已成功应用于工业废料中锑的分析,并采用原子吸收分光光度计法对差示脉冲极谱法的结果进行了比较。

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