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海水痕量金属的浊点萃取及用铱永久性改性剂电热原子吸收光谱法测定

Cloud point extraction of trace metals from seawater and determination by electrothermal atomic absorption spectrometry with iridium permanent modifier.

作者信息

Meeravali Noorbasha N, Reddy M A, Kumar Sunil Jai

机构信息

National Center for Compositional Characterization of Materials, Bhabha Atomic Research Center, Hyderabad, India.

出版信息

Anal Sci. 2007 Mar;23(3):351-6. doi: 10.2116/analsci.23.351.

Abstract

A simple method is described for preconcentration and separation of trace metals such as Ag, Co, Cr, Cu, Fe, Mn, Ni and Pb simultaneously from seawater using a cloud point extraction (CPE) procedure. Triton X-114 nonionic surfactant and ammonium pyrrolidine dithiocarbamate (APDC) have been used as an extraction medium and a chelating extractant, respectively. The amounts of Triton X-114 and APDC and the pH value necessary for extraction were carefully optimized. The preconcentration factor of about 200 is achieved for all the studied metals. Electrothermal atomic absorption spectrometry (ETAAS) with an Ir coated graphite tube as permanent chemical modifier has been used for determination. The limits of detection of Ag, Co, Cr, Cu, Fe, Mn, Ni and Pb were 0.003, 0.008, 0.003, 0.006, 0.015, 0.002, 0.009 and 0.01 ng ml-1, respectively. Certified reference materials such as CASS-4 and NASS-5 (seawater) and NIST-1640 (natural water) have been used for validation of the new method. The relative standard deviation (%) obtained for all the metals are in the range 0.8 - 3.6% for natural water and 11-25% for seawater materials, except for Co in NASS-5 for which it was 50%.

摘要

描述了一种简单的方法,用于使用浊点萃取(CPE)程序同时从海水中预富集和分离痕量金属,如银、钴、铬、铜、铁、锰、镍和铅。分别使用Triton X-114非离子表面活性剂和吡咯烷二硫代氨基甲酸铵(APDC)作为萃取介质和螯合萃取剂。仔细优化了Triton X-114和APDC的用量以及萃取所需的pH值。所有研究的金属都实现了约200的预富集因子。使用涂有铱的石墨管作为永久化学改性剂的电热原子吸收光谱法(ETAAS)进行测定。银、钴、铬、铜、铁、锰、镍和铅的检测限分别为0.003、0.008、0.003、0.006、0.015、0.002、0.009和0.01 ng ml-1。已使用如CASS-4和NASS-5(海水)以及NIST-1640(天然水)等有证标准物质对新方法进行验证。除了NASS-5中的钴相对标准偏差(%)为50%外,所有金属在天然水中获得的相对标准偏差(%)在0.8 - 3.6%范围内,在海水样品中为11 - 25%。

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