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Sulfidation Processes of PVP-Coated Silver Nanoparticles in Aqueous Solution: Impact on Dissolution Rate

机译:PVP包覆的银纳米粒子在水溶液中的硫化过程:对溶出速率的影响

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摘要

Despite the increasing use of silver nanoparticles (Ag-NPs) in nanotechnology and their toxicity to invertebrates, the transformations and fete of Ag-NPs in the environment are poorly understood. This work focuses on the sulfidation processes of PVP-coated Ag-NPs, one of the most likely corrosion phenomena that may happen in the environment. The sulfur to Ag-NPs ratio was varied in order to control the extent of Ag-NPs transformation to silver sulfide (Ag2S). A combination of synchrotron-based X-ray Diffraction (XRD) and Extended X-ray Absorption Fine Structure spectroscopy shows the increasing formation of Ag2S with an increasing sulfur to Ag-NPs ratio. TEM observations show that Ag2S forms nanobridges between the Ag-NPs leading to chain-like struc- tures. In addition, sulfidation strongly affects surface properties of the Ag-NPs in terms of surface charge and dissolution rate. Both may affect the reactivity, transport, and toxicity of Ag-NPs in soils. In particular, the decrease of dissolution rate as a function of sulfide exposure may strongly limit Ag-NPs toxicity since released Ag+ ions are known to be a major factor in the toxicity of Ag-NPs.
机译:尽管在纳米技术中越来越多地使用银纳米颗粒(Ag-NPs),并且它们对无脊椎动物具有毒性,但人们对Ag-NPs在环境中的转化和饱足感知之甚少。这项工作的重点是涂有PVP的Ag-NP的硫化过程,这是环境中最可能发生的腐蚀现象之一。改变硫与Ag-NPs的比例,以控制Ag-NPs转化为硫化银(Ag2S)的程度。基于同步加速器的X射线衍射(XRD)和扩展X射线吸收精细结构光谱的组合显示,随着硫与Ag-NPs的比率增加,Ag2S的形成增加。 TEM观察表明,Ag2S在Ag-NP之间形成纳米桥,从而形成链状结构。另外,硫化在表面电荷和溶解速率方面强烈影响Ag-NP的表面性质。两者均可能影响土壤中Ag-NP的反应性,运输和毒性。特别是,溶解速率的降低作为硫化物暴露的函数可能会强烈限制Ag-NPs的毒性,因为已知释放的Ag +离子是Ag-NPs毒性的主要因素。

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  • 来源
    《Environmental Science & Technology》 |2011年第12期|p.5260-5266|共7页
  • 作者单位

    Surface and Aqueous Geochemistry Group, Department of Geological & Environmental Sciences, Stanford University, Stanford,California 94305-2115, United States,Center for Environmental Implications of NanoTechnology (CEINT), P.O. Box 90287, Duke University, Durham,North Carolina 27708-0287, United States;

    Center for Environmental Implications of NanoTechnology (CEINT), P.O. Box 90287, Duke University, Durham,North Carolina 27708-0287, United States,Department of Civil and Environmental Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, United States;

    Surface and Aqueous Geochemistry Group, Department of Geological & Environmental Sciences, Stanford University, Stanford,California 94305-2115, United States,Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, 2575 Sand Hill Road, Menlo Park,California 94025, United States;

    Department of Chemistry, Universite Pierre et Marie Curie (Paris 6), Paris, France;

    Center for Environmental Implications of NanoTechnology (CEINT), P.O. Box 90287, Duke University, Durham,North Carolina 27708-0287, United States,Department of Civil and Environmental Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, United States;

    Surface and Aqueous Geochemistry Group, Department of Geological & Environmental Sciences, Stanford University, Stanford,California 94305-2115, United States,Center for Environmental Implications of NanoTechnology (CEINT), P.O. Box 90287, Duke University, Durham,North Carolina 27708-0287, United States,Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, 2575 Sand Hill Road, Menlo Park,California 94025, United States;

  • 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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  • 入库时间 2022-08-17 14:03:36

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