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碩士生付嘉琦的論文在TALANTA上刊出
發布時間:2013-01-17     發布者:admin         審核者:     浏覽次數:

标題:Preconcentration and speciation of ultra-trace Se (IV) and Se (VI) in environmental water samples with nano-sized TiO2 colloid and determination by HG-AFS

作者:Fu, JQ(Fu, Jiaqi); Zhang, X(Zhang, Xu ); Qian, SH(Qian, Shahua); Zhang, L(Zhang, Lin)

來源出版物:TALANTA 卷:94頁:167-171 出版年:MAY 30 2012

摘要:A united method for speciation analysis of Se (IV) and Se (VI) in environmental water samples was developed using nano-sized TiO2 colloid as adsorbent and hydride generation atomic fluorescence spectrometry (HG-AFS) as determination means. When the pH values of bulk solution were between 6.0 and 7.0, successful adsorption onto 1 mL nano-sized TiO2 colloid (0.2%) was achieved for more than 97.0% of Se (IV) while Se (VI) barely got adsorbed. Therefore, the method made it possible to preconcentrate and determine Se (IV) and Se (VI) separately. The precipitated TiO2 with concentrated selenium was directly converted to colloid without desorption. Selenium in the resulting colloid was then determined by HG-AFS. The detection limits (3 sigma) and relative standard deviations (R.S.D) of this method were 24 ng/L and 42 ng/L, 7.8% (n = 6) and 7.0% (n = 6) for Se (IV) and Se (VI), respectively. This simple, sensitive, and united method was successfully applied to the separation and speciation of ultra-trace Se (IV) and Se (VI) in environmental water samples.

文獻類型:Article

語種:English

作者關鍵詞:Selenium speciation, Nano-sized TiO2 colloid, HG-AFS

擴展關鍵詞:ATOMIC-ABSORPTION-SPECTROMETRY; OPTICAL-EMISSION-SPECTROMETRY; SOLID-PHASE EXTRACTION; NATURAL-WATER; ACTIVATED CARBON; SELENIUM; SEPARATION; DIOXIDE; SOIL

通訊作者地址:Qian, SH (通訊作者),Wuhan Univ, Hubei Biomass Resource Chem & Environm Biotechnol, Sch Resource & Environm Sci, Wuhan 430079, Peoples R China

地址:

[Fu, Jiaqi; Zhang, Xu; Qian, Shahua; Zhang, Lin] Wuhan Univ, Hubei Biomass Resource Chem & Environm Biotechnol, Sch Resource & Environm Sci, Wuhan 430079, Peoples R China

電子郵件地址:qiansh@whu.edu.cn

學科類别:Chemistry

ISSN:0039-9140

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