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作 者:胡世荣[1] 杨天隆[1] 刘琴英[1] 周丽红[1]
出 处:《分析测试学报》2006年第6期60-62,66,共4页Journal of Instrumental Analysis
基 金:福建省教育基金资助项目(JA04245;JA04277)
摘 要:基于HCl介质中和α,α′-联吡啶存在下,As(V)可催化H2O2氧化2,3,4,9-四氢-9-羟基-1,10-蒽醌(R)转化为无荧光化合物,导致体系荧光急剧猝灭,建立了催化H2O2氧化R荧光猝灭法测定痕量砷的新方法。在最佳条件下,As(V)含量在0.0040~0.40μs/L范围内与荧光强度的△If值呈线性关系,工作曲线的回归方程△If=11.94+233.7 ρAs(V)(μg/L),n=7,相关系数r=0.9994,As(V)检出限为0.62ng/L,n=11。对0.0040和0.40μg/LAs(Ⅴ)分别进行11次的测定,其RSD为2.6%与3.8%。该方法重复性好、灵敏、准确,用于实际样品中砷含量的测定,结果满意。还报道了R的合成,并借助核磁共振潜、红外光谱及质谱等谱学方法确定了其结构。A novel fluorescence method was developed for the determination of arsenic with H2O2 -2, 3,4,9-tetrahydrogen-9-hydroxy-1,10-anthraquinone system. It is based on the catalyzing effect of As ( Ⅴ ) on the fluorescence quenching of 2,3,4,9-tetrahydrogen-9-hydroxy-1,10-anthraquinone (R) by H2O2 in the presence of α,α′-dipyridine in HCl solution. Under optimum conditions, the linear range for As(Ⅴ) was 0. 004 0 -0. 40 μg/L with a correlation coefficient of 0. 999 4 and a detection limit of 0. 62 ng/L. The relative standard deviations for 0. 004 0 μg/L and 0. 40 μg/L As (Ⅴ ) were 2.6% and 3.8% , respectively. The method has been successfully applied to the determination of trace As ( Ⅴ ) in real samples with satisfactory results. The synthesis of R was also reported.
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