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作 者:吴英华[1] 孟杰[2] 马廷升[1] 任凤莲[2]
机构地区:[1]怀化医专公共谋部,湖南怀化418000 [2]中南大学化学化工学院
出 处:《怀化医学高等专科学校学报》2009年第1期25-28,共4页
基 金:湖南省教育厅科研基金资助项目(07C048)
摘 要:运用流动注射分光光度法,系统研究在酸性介质中砷(V)与钼酸铵生成的砷(V)钼杂多酸与丁基罗丹明B显色反应体系。并讨论了吸收曲线、酸度、显色剂与表面活性剂PVA的用量、泵转速、进样时间、共存组分及干扰元素对测定结果的影响。结果表明:As(V)在0.0~0.16mg/L浓度范围内与吸光度有良好的线性关系,线性回归方程为A=0.0706+1.4413c,线性相关系数为0.9943,相对标准偏差为0.36%,检测限为0.0075mg/L,对废水中的As(V)进行测定,加标回收率在96.84%~107.46%之间。It is found that in acid medium arsenic (V) could react with ammonium molybdate to form heteromolybdoarsenic acid. In this paper, the developing system between hteromolybdoarsenic acid and butyl rhodamine B was systematically investigated by flow injection spectrophotometry. The effect of some conditions, such as the absorption curve, acidity, chromogenic reagent, rotate speed, sampling time, coexisting ions and polyvinyl alcohol (PVA} were studied. The results showed that under the optimum conditions the linear range of As was 0.0 - 0.16 mg/L, the linear regression equation was A = 0.0706 + 1.4413c (R = 0.9943), the detection limit was 0.0075 mg/L, the relative standard deviation (RSD) was 0.36% and the recovery of the method was founded to be 96.84% - 107.46% when determined arsenic in the waste water.
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