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Transport of two metal oxide nanoparticles in saturated granular porous media: Role of water chemistry and particle coating

机译:两种金属氧化物纳米颗粒在饱和颗粒多孔介质中的传输:水化学和颗粒涂层的作用

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The growing use of nanosized titanium dioxide (nTiO_2) and zinc oxide (nZnO) in a large number of commercial products raises concerns regarding their release and subsequent mobility in natural aquatic environments. Laboratory-scale sand-packed column experiments were conducted with bare and polymer-coated nTiO_2 and nZnO to improve our understanding of the mobility of these nanoparticles in natural or engineered water saturated granular systems. The nanoparticles are characterized over a range of environmentally relevant water chemistries using multiple complimentary techniques: dynamic light scattering, nanoparticle tracking analysis, transmission electron microscopy, and scanning electron microscopy. Overall, bare (uncoated) nanoparticles exhibit high retention within the water saturated granular matrix at solution ionic strengths (IS) as low as 0.1 mM NaNO_3 for bare nTiO_2 and 0.01 mM NaNO_3 for bare nZnO. Bare nTiO_2 and nZnO also display dynamic (time-dependent) deposition behaviors under selected conditions. In contrast, the polymer-coated nanoparticles are much less likely to aggregate and exhibit significant transport potential at IS as high as 100 mM NaNO_3 or 3 mM CaCl_2. These findings illustrate the importance of considering the extent and type of surface modification when evaluating metal oxide contamination potential in granular aquatic environments.
机译:纳米二氧化钛(nTiO_2)和氧化锌(nZnO)在大量商业产品中的使用日益增加,引起了人们对其释放以及随后在天然水生环境中迁移的担忧。使用裸露的和聚合物涂覆的nTiO_2和nZnO进行了实验室规模的装沙柱实验,以提高我们对这些纳米粒子在天然或工程用水饱和粒状系统中的迁移率的了解。使用多种互补技术在一系列与环境相关的水化学特征中对纳米颗粒进行表征:动态光散射,纳米颗粒跟踪分析,透射电子显微镜和扫描电子显微镜。总体而言,裸露的(未涂覆)纳米颗粒在溶液离子强度(IS)下对水饱和的颗粒状基质表现出较高的保留力,对于裸露的nTiO_2,离子强度低至0.1 mM NaNO_3,对于裸露的nZnO,其离子强度低至0.01 mM NaNO_3。裸露的nTiO_2和nZnO在选定条件下也显示出动态的(随时间变化)沉积行为。相反,涂有聚合物的纳米颗粒在IS高达100 mM NaNO_3或3 mM CaCl_2的情况下,聚集的可能性较小,并显示出显着的运输潜力。这些发现说明了在评估颗粒水生环境中金属氧化物污染潜力时考虑表面改性程度和类型的重要性。

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