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Adsorptive Voltammetric Studies on the Cerium(III)–Alizarin Complexon Complex at a Carbon Paste Electrode

机译:碳糊电极上铈(III)-茜素配合物络合物的吸附伏安研究

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摘要

A novel procedure was developed for the determination of trace cerium on the basis of anodic adsorption voltammetry of the Ce(III)–alizarin complexon (ALC) complex at a carbon paste electrode (CPE). The procedure is convenient to determine cerium individually in the presence of other rare earths because there is a 100 mV difference between the peak potentials of Ce(III)–ALC and other rare earth(III)–ALC complexes in a supporting electrolyte of 0.08 M HAc–NaAc and 0.012 M potassium biphthalate (pH 4.7) when performing linear-scanning from −0.2 to 0.8 V (vs. SCE) at 100 mV/s. The second-order derivative peak currents are directly proportional to the Ce(III) concentration over a range of 6.0 × 10−9–3.0 × 10−7 M. The detection limit is as low as 2.0 × 10−9 M (S/N = 3) for a 120 s preconcentration. An RSD of 3.5% was obtained for 15 determinations of Ce(III) at a concentration of 4.0 × 10−8 M on the same CPE surface. The method was applied successfully to the determination of cerium in samples of rare earth nodular graphite cast iron.
机译:在碳糊电极(CPE)上,Ce(III)-茜素络合物(ALC)络合物的阳极吸附伏安法的基础上,开发了一种测定痕量铈的新方法。在0.08 M的支持电解质中,Ce(III)–ALC和其他稀土(III)–ALC络合物的峰电位之间存在100 mV的差异,因此该方法在存在其他稀土元素的情况下方便地单独测定铈。当以100 mV / s的速度从-0.2到0.8 V(相对于SCE)进行线性扫描时,HAc-NaAc和0.012 M的邻苯二甲酸钾(pH 4.7)。在6.0×10−9 –3.0×10−7 M范围内,二阶导数峰值电流与Ce(III)浓度成正比。检测极限低至2.0 ×10−9 M(S / N = 3)进行120 s预浓缩。在同一CPE表面上以4.0×10-8 M的浓度进行15次Ce(III)测定的相对标准偏差为3.5%。该方法已成功应用于稀土球墨铸铁样品中铈的测定。

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