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甲基紫电极EDTA电位滴定法测定微量铅

Determination of trace leadⅡ by EDTA potential titration using methyl violet ion selective electrode

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【作者】 何智娟董学芝胡卫平

【Author】 HE Zhi-juan, DONG Xue-zhi~*, HU Wei-ping(Department of Chemistry,Henan University,Kaifeng 475001,China)

【机构】 河南大学化学化工学院河南大学化学化工学院 河南开封 475001河南开封 475001河南开封 475001

【摘要】 提出了在氨三乙酸(NTA,活化剂)存在下,以Mn 催化高碘酸钾氧化甲基紫的反应指示滴定终点,以自制的甲基紫选择性电极为指示电极,Mn 为滴定剂,EDTA为阻抑剂,催化电位滴定法测定微量铅的新方法。实验表明,选择1 0×10-3mol/L甲基紫溶液、5 0×10-3mol/LKIO4溶液和5 0×10-3mol/LNTA溶液用量分别为0 50,1 00,0 50mL,滴定速度1 7mL/min,终点灵敏,准确度高。将该方法用于蓄电池废水中铅含量测定,结果与火焰原子吸收光谱法一致,样品平均回收率为99 1%,RSD为1 47%。

【Abstract】 A new potential titration with catalytic indicating end point for the determination of trace lead is described. Based on the catalytic effect of manganese*" on the oxidation of methyl violet(MV) by potassium periodate in the presence of nitrilotriacetic acid(NTA), a new kind of methyl violet ion selective electrode made by ourselves is used for inspecting the change of potential,and manganese*" is served as a titrant and EDTA is served as a inhibitor in the titration.The results show when the volume of 1.0×10-3 mol/L MV solution,5.0×10-3 mol/L KIO4 solution,5.0×10-3 mol/L NTA solution is 0.50,1.00,0.50 mL respectively,and the chosen rate of titration is 1.7 mL/min.The method has high sensitivity and good accuracy.It has been applied to the determination of lead*" in the waste water of storage battery and the results determined by this method is agreed with those by atomic absorption spectrometry.The average recovery of sample is 99.1%,and the relative standard deviation is 1.47%.

  • 【文献出处】 冶金分析 ,Metallurgical Analysis , 编辑部邮箱 ,2005年02期
  • 【分类号】X830;O657.15
  • 【被引频次】3
  • 【下载频次】156
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