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An investigation on the aggregation phenomena of Titanium dioxide nanoparticles in natural waters: role of ionic strength, and organic matter

机译:天然水中二氧化钛纳米粒子聚集现象的研究:离子强度和有机物的作用

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The aggregation of TiO_2 nanoparticles under different aqueous matrixes representative of natural waters was experimentally investigated. Conditions included indiferent electrolytes (NaCl) and specifically adsorbing cations (CaCl_2 and MgCl_2), in the presence and absence of natural organic matter. The nanoparticles of 21 nm primary particle size, formed stable aggregates of aproximately 250 nm under conditions unfavorable for aggregation, while size increased significantly at pHs near or at the pzc of the material (pzc TiO_2 6.3). The pH for favorable aggregation was affected by the presence of divalent cations and natural organic matter, turning the nanoparticles mobile at conditions were otherwise limited mobility should be expected. DLVO calculations confirmed the experimental observations, if the stable aggregate size was applied as the primary size of the particles. Aggregate morphology observed by SEM was in agreement with proposed mechanisms.
机译:实验研究了代表天然水的不同水性基质下TiO_2纳米粒子的聚集。条件包括在存在和不存在天然有机物的情况下,不同的电解质(NaCl),特别是吸附阳离子(CaCl_2和MgCl_2)。在不利于聚集的条件下,具有21 nm初级粒径的纳米颗粒形成了约250 nm的稳定聚集体,而在接近或超过材料pzc的pH值(pzc TiO_2 6.3)时,粒径显着增加。用于有利聚集的pH受二价阳离子和天然有机物的存在的影响,使纳米颗粒在一定条件下可移动,否则应限制迁移率。如果将稳定的聚集体尺寸用作颗粒的主要尺寸,则DLVO计算证实了实验观察结果。 SEM观察到的聚集体形态与所提出的机理相符。

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