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作 者:曾美云[1] 王迪民[1] 陈燕波[1] 杨梅[1] 宋松[1]
机构地区:[1]国土资源部武汉地质矿产研究所,湖北武汉430205
出 处:《岩矿测试》2011年第4期501-504,共4页Rock and Mineral Analysis
基 金:国土资源地质大调查项目(1212010816029)
摘 要:二苯碳酰二肼光度法是测定微量Cr(Ⅵ)的行业标准方法,以硫酸作为显色介质,酸度要求严格,显色稳定时间短,体系显色后需在10 min~1 h测定完毕,灵敏度较差。本文对标准方法进行改进,将显色介质由硫酸改为磷酸。结果表明,在H3PO4介质中显色剂与Cr(Ⅵ)反应生成的络合物可稳定3 h,方法相对标准偏差(RSD)≤5.25%,加标回收率为99.2%~102.0%,检出限由标准方法的13.6μg/g降至3.8μg/g。建立的方法用于超基性岩标准物质分析,相比于标准方法,稳定性、精密度和准确性均有提高。Diphenylcarbazide Spectrophotometry is a standard method to measure trace Cr(Ⅵ).However,using H2SO4 as the chromogenic medium has limitations such as a strict sulfuric acid concentration,short stability time of 10-60 min and poor sensitivity.An improvement was made to the diphenylcarbazide spectrophotometric method by replacing sulfuric acid with phosphoric acid as the chromogenic medium.Results indicate that the reaction is stable for 3 h in the phosphoric medium,and the detection limit is reduced from 13.6 μg/g to 3.8 μg/g with a recovery factor of 99.2%-102.0% and RSD≤5.25%.Compared with the routine method,the improved method,when applied to ultramafic rock standard materials demonstrates higher stabilization,precision and accuracy.
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