Ma Huan, Dai Lenore L
Department of Chemical Engineering, Arizona State University, Tempe, Arizona 85287, USA.
Langmuir. 2009 Oct 6;25(19):11210-5. doi: 10.1021/la9021036.
We have successfully assembled two-component S-PS/AS-PS (sulfate-treated polystyrene/aldehyde sulfate-treated polystyrene) and three-component S-PS/AS-PS/C-PS (sulfate-treated polystyrene/aldehyde sulfate-treated polystyrene/carboxylate-treated polystyrene) colloidal lattices at poly(dimethylsiloxane)-water interfaces. The colloidal particles assemble 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 sixfold lattice sites, whereas the AS-PS particles largely form fivefold defect sites. The calculated attractive capillary force is stronger for the AS-PS particles, which likely explains their tendency to aggregate compared to the S-PS particles. In addition, we have performed total force calculation and extrapolated the surface charge densities of the particles in the oil phase.
我们已成功在聚二甲基硅氧烷 - 水界面组装了双组分S - PS/AS - PS(硫酸盐处理的聚苯乙烯/醛硫酸盐处理的聚苯乙烯)和三组分S - PS/AS - PS/C - PS(硫酸盐处理的聚苯乙烯/醛硫酸盐处理的聚苯乙烯/羧酸盐处理的聚苯乙烯)胶体晶格。胶体颗粒组装成具有长程有序的结构,并在其平衡位置附近振荡。不同类型的颗粒随机分布在晶格中,没有明显的相分离。在双组分胶体晶格中,S - PS颗粒大多形成六重晶格位点,而AS - PS颗粒主要形成五重缺陷位点。计算得出,AS - PS颗粒的吸引力毛细力更强,这可能解释了它们与S - PS颗粒相比更易聚集的趋势。此外,我们进行了总力计算,并推断了油相中颗粒的表面电荷密度。