砷钼杂多酸-乙基罗丹明B流动注射分光光度法测定地表水中砷(Ⅴ)  被引量:4

Heteromolybdoarsenic acid-ethyl rhodamine B flow injection spectrophotometric determination of arsenic(Ⅴ) in surface water

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作  者:陈国和[1] 张新申[1] 龚正君[2] 肖新峰[3] 

机构地区:[1]四川大学轻纺与食品学院,四川成都610065 [2]西南交通大学环境科学与工程学院,四川成都610031 [3]山东科技大学工程学院,山东泰安271021

出  处:《冶金分析》2006年第3期44-46,共3页Metallurgical Analysis

基  金:国家863项目(2002AA639290)

摘  要:在0.5mol/L硝酸介质中,砷(Ⅴ)能与钼酸铵形成砷钼杂多酸,在表面活性剂聚乙烯醇(PVA)存在下,砷钼杂多酸可以和乙基罗丹明B(ERB)生成可溶于水的络合物,该络合物在605nm处有最大吸收,据此建立了流动注射分光光度法直接测定地表水中砷(Ⅴ)的方法。砷(Ⅴ)在1.0~100μg/L质量浓度范围内符合比尔定律,检出限为0.1μg/L,平行测定40μg/L砷(Ⅴ)14次,相对标准偏差为3.06%。方法用于实际水样分析,回收率在92.6%~105.1%之间,测定结果与原子吸收光谱法基本一致。It is found that in 0.5 mol/L nitric acid medium arsenic(Ⅴ) reacts with ammonium molybdate to form heteromolybdoarsenic acid,which forms a soluble complex with ethyl rhodamine B in the presence of polyvinyl alcohol(PVA). The complex has maximum absorption at 605 nm. Beer's law is obeyed in the concentration range of 1.0-100μg/L for arsenic(Ⅴ).Based on this, a new flow injection spectrophotometric method for the determination of trace arsenic in surface water was proposed. The relative standard deviation of 3.06 % was obtained by injecting 40μg/L of As(Ⅴ) standard solution( n=14). The detection limit calculated from three times of the average background noise was 0.1μg/L. The recoveries of surface water samples were between 92.6% and 105.1%, and the determination results were in good agreement with those obtained by AAS.

关 键 词: 流动注射分光光度法 砷钼杂多酸 乙基罗丹明B 

分 类 号:X832[环境科学与工程—环境工程]

 

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