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Tracking the Transformation of Nanoparticulate and Ionic Silver at Environmentally Relevant Concentration Levels by Hollow Fiber Flow Field-Flow Fractionation Coupled to ICPMS

机译:通过与ICPMS耦合的中空纤维流场流分馏跟踪与环境有关的浓度水平下的纳米粒子和离子银的转变

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摘要

It is a great challenge to monitor the physical and chemical transformation of nanoparticles at environmentally relevant concentration levels, mainly because the commonly used techniques like dynamic light scattering and transmission electron microscopy are unable to characterize and quantify trace level nanoparticles in complex matrices. Herein, we demonstrate the on-line coupled system of hollow fiber flow field-flow fractionation (HF5), minicolumn concentration, and inductively coupled plasma mass spectrometry (ICPMS) detection as an efficient approach to study the aggregation and chemical transformation. of silver nanoparticles (AgNPs) and ionic Ag species in the aqueous environment at ng/mL levels. Taking advantage of the in-line dialysis of HF5, the selective capture of Ag(I) species by the resin in minicolumn, and the high selectivity and sensitivity of ICPMS detection, we recorded the aggregation of 10 ng/mL AgNPs in complex matrices (e.g., NOM, Na~+/Ca~(2+)), revealing an interesting tiny AgNPs formation process of photoreduction of trace level Ag(l) that is different from larger AgNPs generated at high concentration of Ag(l) by accurate characterization and respectively identifying and quantifying new thiol-complexed Ag(l) and residual Ag(l) in the intertransformation of Ag(I) and AgNPs in domestic wastewater by simultaneously detecting the S and Ag signals via ICPMS.
机译:在与环境有关的浓度水平下监测纳米颗粒的物理和化学转化是一个巨大的挑战,这主要是因为常用的技术(例如动态光散射和透射电子显微镜)无法表征和量化复杂基质中的痕量纳米颗粒。在此,我们演示了中空纤维流场流分馏(HF5),小柱浓度和电感耦合等离子体质谱(ICPMS)检测的在线耦合系统,作为研究聚集和化学转化的有效方法。 ng / mL浓度的水环境中的银纳米颗粒(AgNPs)和离子Ag种类。利用HF5的在线透析,微型柱中树脂对Ag(I)物种的选择性捕获以及ICPMS检测的高选择性和灵敏度,我们记录了10 ng / mL AgNP在复杂基质中的聚集(例如NOM,Na〜+ / Ca〜(2+)),揭示了一种有趣的微小AgNPs形成过程,该过程具有痕量Ag(l)的光还原作用,该过程不同于通过精确表征在高浓度Ag(l)下生成的较大AgNP并通过ICPMS同时检测S和Ag信号,分别识别和量化生活用水中Ag(I)和AgNPs互变中新的硫醇复合Ag(l)和残留的Ag(l)。

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  • 来源
    《Environmental Science & Technology》 |2017年第21期|12369-12376|共8页
  • 作者单位

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

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

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

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

    Department of Chemistry, Yonsei University, Seoul 03722, Korea;

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

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

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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