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机构地区:[1]中国广州分析测试中心,广东省分析测试技术公共实验室,广东广州510070
出 处:《光谱学与光谱分析》2011年第11期3123-3125,共3页Spectroscopy and Spectral Analysis
基 金:国家自然科学基金项目(20807012);广东省自然科学基金项目(9151065003000010)资助
摘 要:用HNO3+HCl分解样品,采用Fe3+-柠檬酸混合溶液作抑制剂,研究了下氢化物发生-原子荧光光谱法测定痕量硒时的干扰及其机理,探讨了NO3-和NO2-残留的影响,并用正交试验设计结合单因素试验研究了不同浓度Fe3+盐、盐酸、柠檬酸、硼氢化钾等条件下Se的回收率。该方法的检出限为0.15μg.L-1,样品中Se含量为27.01μg.L-1的相对标准偏差在3.1%~4.2%之间(n=11),加标回收率为96.1%~102.3%。用于实际样品的测定,结果满意。The samples were decomposed with HNO3+HCl,and Fe3+-citric acid mix solution was added to eliminate interferences.The elimination and mechanism of tellurium interference with selenium determination by HG-AFS were studied,and the residuary influence of NO-3 and NO-2 was investigated.The interference of ferric trichloride,hydrochloric acid,citric acid and PBH concentration with the fluorescence intensity of selenium was observed by the orthogonal test design combined with the mono-factor test.The detection limit was 0.15 μg·L-1.The relative standard deviation of a solution containing 27.01 μg·L-1 selenium in sample was in the range of 3.1%~4.2%(n=11),and the recoveries of selenium were 96.1%~102.3%.The results obtained were satisfied,and the method was successfully applied to the determination of selenium in high purity tellurium samples.
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