期刊文献+

稀土化学修饰电极的研究——铕(Ⅲ)的电化学行为 被引量:6

Rare Earth Chemically Modified Electrode——Electrochemical Behaviour of Europium(Ⅲ)
下载PDF
导出
摘要 本文研究了铕(Ⅲ)在Nafion聚合物薄膜化学修饰电极上的电化学行为。研究结果表明,在pH5.8的醋酸缓冲溶液中,铕(Ⅲ)的氧化还原非常接近可逆过程。利用二甲酚橙的络合作用和Nafion的阳离子交换作用,在选定条件下,铕(Ⅲ)的导数波高度与其浓度在2.0×10^(-7)~1.0×10^(-5)mol/L范围内成线性关系,检出限为1.0×10^(-7)mol/L。当富集时间为10min时,检出限可达2.0×10^(-8)mol/L,Sm(Ⅲ)、Yb(Ⅲ)及其他稀土元素基本不干扰,可用于铕(Ⅲ)的分析测定。同时避免了使用汞(Ⅱ)的问题。 Electrochemical behaviour of Eu(Ⅲ) at a Nafion polymer film electrode was studied by using cyclic voltammetry. The result showed that the electrochemical reaction of Eu(Ⅲ) in acetic buffer solution (pH 5.8) at a Nafion film electrode is nearly a reversible process. A sensitive stripping voltammetry method for the determination of Eu(Ⅲ) was proposed in the presence of xylenol orange (XO) as a ligand at the Nafion film electrode. In the solution of 0.1mol/L HAc-NaAc (pH2.9) containning 1.0×10^(-4)mol/L of XO, cathodic scanning from -0.2 to -1.5V, (vs. SCE) at sweep rate of 200mV/s after 1 min at-0.2V, the reduction wave of Eu(Ⅲ)-XO at about -1.2V was recorded, The peak current is proportional to the concentration of Eu(Ⅲ) in the range of 2.0×10^(-7)~1.0×10^(-5) mol/L with a detection limit of 1.0×10^(-7)mol/L. When the accumulated time at -0.2 V was increased to 10min, the detection limit was below 2.0×10^(-8) mol/L. No interferences of Sm(Ⅲ), Yb(Ⅲ) and other rare earth ions were observed. And the mercury pollution in the method could be avoided.
出处 《分析化学》 SCIE EI CAS CSCD 北大核心 1991年第12期1373-1378,共6页 Chinese Journal of Analytical Chemistry
关键词 化学修饰电极 电化学 稀土 Europium, Chemically modified electrode, Nafion film
  • 相关文献

参考文献9

  • 1董绍俊,Electroanalysis,1989年,1卷,99页
  • 2金利通,仝威,方禹之.聚合物型修饰电极及其在分析化学中的应用[J].分析试验室,1989,8(1):42-50. 被引量:6
  • 3Lu Z,J Chem Soc Faraday Trans I,1988年,84卷,9期,2979页
  • 4董绍俊,分析化学,1988年,16卷,10期,951页
  • 5Lu Z,J Electroanal Chem,1987年,233卷,19页
  • 6方禹之,1987年全国电分析化学学术论文集.下,1987年
  • 7董绍俊,分析化学,1985年,13卷,11期,870页
  • 8张曼平,中国科学.B,1982年,25B卷,398页
  • 9Gao X,Handbook on the Physics Chemistry of Rare Earth Elements

二级参考文献2

共引文献5

同被引文献929

引证文献6

二级引证文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部