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Stability of highly asymmetric binary colloidal dispersions and their application to film formation.

机译:高不对称二元胶体分散体的稳定性及其在成膜中的应用。

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摘要

Binary waterborne suspensions of hard and soft particles can yield tough, impervious, crack-free films when hard-particle percolation is suppressed in the drying process. Small soft colloids can be distributed around large hard colloids by coupling particle size asymmetry with surface potential asymmetry in the blend, according to recent experiments where highly charged zirconia nanoparticles formed adsorbed layers around nearly-neutral silica microspheres. Yet, the phase behavior of highly asymmetric silica-zirconia blends is rather complex, and the underlying mechanism has remained a subject of debate. We contribute detailed microstructure calculations and explore the driving forces affecting stability of these blends.;Our model of the silica-zirconia blends at experimental conditions suggests that colloid-nanoparticle attraction of electrostatic origin assembles an adsorbed layer, a halo, of nanoparticles around each colloid. When nanoparticle halos are sufficiently dense, electrostatic stabilization of the silica colloids against van der Waals flocculation is predicted. Meanwhile, further densification of the charged halos leads to well-defined nanoparticle depletion zones adjacent to the halos. These depletion zones provide an entropic incentive for the haloed colloids to aggregate, destabilizing the blend. Detailed calculations of effective colloid-colloid interactions, as well as estimates of rheological behavior, are in qualitative agreement with existing experiments.;Our computational findings motivate an aqueous formulation that is less size-asymmetric and consists of silica microspheres and deformable acrylic latex spheres with the size ratio of 5:1, respectively. Composite films, cast from these blends at various pH, are studied via scanning electron microscopy and thermogravimetric analysis. The suspension pH, which sets the surface potential of silica colloids, is correlated with radial and crosssectional uniformity of dried films. Low-pH precursor suspensions yield uniform composite films with solids loading up to 71% by volume that remain crack-free.
机译:当在干燥过程中抑制硬颗粒的渗滤时,硬颗粒和软颗粒的二元水性悬浮液会产生坚韧,不渗透的无裂纹膜。根据最近的实验,在混合物中,高电荷的氧化锆纳米粒子会在几乎中性的二氧化硅微球周围形成吸附层,从而通过在混合物中将粒径不对称性与表面电势不对称性耦合,可以将小的软胶体分布在大的硬胶体周围。然而,高度不对称的二氧化硅-氧化锆共混物的相行为相当复杂,其潜在机理仍是争论的话题。我们提供了详细的微观结构计算并探讨了影响这些共混物稳定性的驱动力。;我们在实验条件下制备的二氧化硅-氧化锆共混物模型表明,静电源的胶体-纳米颗粒吸引力在每个胶体周围组装了纳米颗粒的吸附层,即光晕。当纳米颗粒晕足够致密时,可以预测二氧化硅胶体对范德华絮凝的静电稳定作用。同时,带电光晕的进一步致密化导致与光晕相邻的轮廓分明的纳米颗粒耗尽区。这些耗尽区为光晕的胶体聚集提供了熵激励,破坏了混合物的稳定性。有效胶体-胶体相互作用的详细计算以及流变行为的估计与现有实验在质量上是一致的;我们的计算发现促使了一种尺寸不对称性较小的水性配方,该配方由二氧化硅微球和可变形的丙烯酸乳胶球组成。大小比例分别为5:1。通过扫描电子显微镜和热重分析研究了在各种pH下由这些共混物浇铸的复合膜。悬浮液的pH值决定了二氧化硅胶体的表面电势,它与干膜的径向和横截面均匀性相关。低pH前体悬浮液可产生均匀的复合膜,其中固体含量高达71%(体积),并且保持无裂纹。

著录项

  • 作者

    Shcherbakov, Denis A.;

  • 作者单位

    Princeton University.;

  • 授予单位 Princeton University.;
  • 学科 Chemical engineering.
  • 学位 Ph.D.
  • 年度 2014
  • 页码 207 p.
  • 总页数 207
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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