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Structure of Multi-Component Colloidal Lattices at Oil-Water Interfaces

机译:油水界面多组分胶体晶格的结构

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We have successfully assembled two-component S-PS/AS-PS (sulfate-treatedpolystyrene/aldehyde sulfate-treated polystyrene) and three-component S-PS/AS-PS/C-PS(sulfate-treated polystyrene/aldehyde sulfate-treated polystyrene/carboxylate-treatedpolystyrene) colloidal lattices at poly(dimethylsiloxane)-water interfaces. The colloidal particlesassemble into long-range ordered structure and oscillate around their equilibrium positions.Different types of particles distribute randomly in the lattice with no obvious phase separation.In the two-component colloidal lattices, the S-PS particles form mostly 6-fold lattice sites,whereas the AS-PS particles largely form 5-fold defect sites. The calculated attractive capillaryforce is stronger for the AS-PS particles, which likely explains their tendency of aggregationcompared to the S-PS particles. In addition, we have performed total force calculation andextrapolated the surface charge densities of the particles in the oil phase.
机译:我们已经成功组装了两组分S-PS / AS-PS(经过硫酸处理 聚苯乙烯/硫酸乙醛处理的聚苯乙烯)和三组分S-PS / AS-PS / C-PS (硫酸处理的聚苯乙烯/硫酸醛处理的聚苯乙烯/羧酸盐处理的 聚(二甲基硅氧烷)-水界面处的聚苯乙烯)胶体晶格。胶体颗粒 组装成远程有序结构,并在其平衡位置附近振荡。 不同类型的粒子随机分布在晶格中,没有明显的相分离。 在两组分胶体晶格中,S-PS颗粒主要形成6倍晶格位, 而AS-PS颗粒主要形成5倍缺陷位。计算出的吸引毛细管 AS-PS颗粒的作用力更大,这可能解释了它们的聚集趋势 与S-PS颗粒相比。此外,我们还进行了总力计算和 外推油相中颗粒的表面电荷密度。

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