催化光度返滴定法测定微量锰的研究  被引量:3

Study on Catalytic Spectrophotometric Back Titrimetry for Determining Trace Manganese

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作  者:秦永惠[1] 李潞铭[1] 王芳 

机构地区:[1]河北大学化学系

出  处:《分析试验室》1997年第3期68-71,共4页Chinese Journal of Analysis Laboratory

摘  要:本文研究了催化光度返滴定法测定微量锰的原理,找到最佳实验条件,确立了实验方法。测定波长622nm;反应时间1min40s;活化剂NTA用量0.60mL;KIO4与孔雀石绿用量比为1.00∶0.35;室温下滴定;用pH=5.4的乙酸-乙酸钠缓冲溶液控制溶液酸度;测定Mn2+的浓度范围为1×10-7~1×10-5mol/L;Co2+、Bi3+、Ca2+、Al3+、Pb2+、Cu2+、Zn2+、Fe2+、Mg2+等离子均不干扰测定。该法具有较高灵敏度和准确度。试用于黄豆和化学试剂MgSO4中锰的测定,结果令人满意。In this article the catalytic spectrophotometric back titrimetry for determining trace manganese was studied,best experimental conditions were selected and experimental method was established.The determination wavelength is 622nm and the reaction time is 1min 40sec.The volume of activating agent NTA is 0.60mL.Volume ratio between KIO 4 and malachite green is 1.00∶0.35.The titration is done at room temperature with the acidity of solution controled by HAc NaAc buffer solution(pH=5 4).The concentration range for determining manganese is 1×10 -7 ~1×10 -5 mol/L Co 2+ 、Bi 3+ 、Ca 2+ 、Al 3+ 、Pb 2+ 、Cu 2+ 、Zn 2+ 、Fe 2+ and Mg 2+ do not interfere with the determination.This method has higher sensitivity and accuracy.Manganese in soybean and chemical agent MgSO 4 was determined with satisfactory results.

关 键 词:催化 光度返滴定法  

分 类 号:O614.711[理学—无机化学]

 

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