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中空纤维支撑液膜萃取法对纳米银分散体和环境水样中可动态和总态一价银的形态分析。

Speciation Analysis of Labile and Total Silver(I) in Nanosilver Dispersions and Environmental Waters by Hollow Fiber Supported Liquid Membrane Extraction.

机构信息

State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Science, Chinese Academy of Sciences , Beijing 100085, China.

Chemical Metrology and Analytical Science Division, National Institute of Metrology , P. R. China , Beijing 100029.

出版信息

Environ Sci Technol. 2015 Dec 15;49(24):14213-20. doi: 10.1021/acs.est.5b02917. Epub 2015 Nov 30.

DOI:10.1021/acs.est.5b02917
PMID:26580982
Abstract

Hollow fiber supported liquid membrane (HFSLM) extraction was coupled with ICP-MS for speciation analysis of labile Ag(I) and total Ag(I) in dispersions of silver nanoparticles (AgNPs) and environmental waters. Ag(I) in aqueous samples was extracted into the HFSLM of 5%(m/v) tri-n-octylphosphine oxide in n-undecane, and stripped in the acceptor of 10 mM Na2S2O3 and 1 mM Cu(NO3)2 prepared in 5 mM NaH2PO4-Na2HPO4 buffer (pH 7.5). Negligible depletion and exhaustive extraction were conducted under static and 250 rpm shaking to extract the labile Ag(I) and total Ag(I), respectively. The extraction equilibration was reached in 8 h for both extraction modes. The extraction efficiency and detection limit were (2.97 ± 0.25)% and 0.1 μg/L for labile Ag(I), and (82.3 ± 2.0)% and 0.5 μg/L for total Ag(I) detection, respectively. The proposed method was applied to determine labile Ag(I) and total Ag(I) in different sized AgNP dispersions and real environmental waters, with spiked recoveries of total Ag(I) in the range of 74.0-98.1%. With the capability of distinguishing labile and total Ag(I), our method offers a new approach for evaluating the bioavailability and understanding the fate and toxicity of AgNPs in aquatic systems.

摘要

中空纤维支撑液膜(HFSLM)萃取与 ICP-MS 联用,用于分析分散态银纳米颗粒(AgNPs)和环境水中不稳定 Ag(I)和总 Ag(I)的形态。水样中的 Ag(I)被萃取到正辛基膦酸三正己酯(TOPO)在正十一烷中的 HFSLM 中,在 5mMNaH2PO4-Na2HPO4 缓冲液(pH7.5)中的 10mMNa2S2O3 和 1mM Cu(NO3)2 接受相中进行洗脱。在静态和 250rpm 搅拌下进行轻微耗尽和完全萃取,分别萃取不稳定 Ag(I)和总 Ag(I)。两种萃取模式的萃取平衡均在 8 小时内达到。对于不稳定 Ag(I)的萃取效率和检测限分别为(2.97±0.25)%和 0.1μg/L,对于总 Ag(I)的萃取效率和检测限分别为(82.3±2.0)%和 0.5μg/L。该方法用于测定不同粒径 AgNP 分散体和实际环境水中的不稳定 Ag(I)和总 Ag(I),总 Ag(I)的加标回收率在 74.0-98.1%范围内。该方法具有区分不稳定 Ag(I)和总 Ag(I)的能力,为评估 AgNPs 在水生系统中的生物可利用性和了解其归宿和毒性提供了一种新方法。

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