Simovic Spomenka, Prestidge Clive A
Ian Wark Research Institute, ARC Special Research Centre for Particle and Material Interfaces, University of South Australia, Mawson Lakes, SA 5095, Australia.
Langmuir. 2004 Sep 14;20(19):8357-65. doi: 10.1021/la0491807.
The coalescence stability of poly(dimethylsiloxane) emulsion droplets in the presence of silica nanoparticles ( approximately 50 nm) of varying contact angles has been investigated. Nanoparticle adsorption isotherms were determined by depletion from solution. The coalescence kinetics (determined under coagulation conditions at high salt concentration) and the physical structure of coalesced droplets were determined from optical microscopy. Fully hydrated silica nanoparticles adsorb with low affinity, reaching a maximum surface coverage that corresponds to a close packed monolayer, based on the effective particle radius and controlled by the salt concentration. Adsorbed layers of hydrophilic nanoparticles introduce a barrier to coalescence of approximately 1 kT, only slightly reduce the coalescence kinetics, and form kinetically unstable networks at high salt concentrations. Chemically hydrophobized silica nanoparticles, over a wide range of contact angles (25 to >90 degrees ), adsorb at the droplet interface with high affinity and to coverages equivalent to close-packed multilayers. Adsorption isotherms are independent of the contact angle, suggesting that hydrophobic attraction overcomes electrostatic repulsion in all cases. The highly structured and rigid adsorbed layers significantly reduce coalescence kinetics: at or above monolayer surface coverage, stable flocculated networks of droplets form and, regardless of their wettability, particles are not detached from the interface during coalescence. At sub-monolayer nanoparticle coverages, limited coalescence is observed and interfacial saturation restricts the droplet size increase. When the nanoparticle interfacial coverage is >0.7 and <1.0, mesophase-like microstructures have been noted, the physical form and stability of which depends on the contact angle. Adsorbed nanoparticle layers at monolayer coverage and composed of a mixture of nanoparticles with different hydrophobisation levels form stable networks of droplets, whereas mixtures of hydrophobized and hydrophilic nanoparticles do not effectively stabilize emulsion droplets.
研究了在存在不同接触角的二氧化硅纳米颗粒(约50 nm)时聚二甲基硅氧烷乳液液滴的聚并稳定性。通过溶液中的耗尽法测定纳米颗粒吸附等温线。聚并动力学(在高盐浓度的凝聚条件下测定)和聚并液滴的物理结构通过光学显微镜确定。完全水合的二氧化硅纳米颗粒以低亲和力吸附,基于有效颗粒半径并受盐浓度控制,达到对应于紧密堆积单层的最大表面覆盖率。亲水性纳米颗粒的吸附层引入了约1 kT的聚并屏障,仅略微降低聚并动力学,并在高盐浓度下形成动力学不稳定网络。化学疏水化的二氧化硅纳米颗粒在很宽的接触角范围(25至>90度)内以高亲和力吸附在液滴界面上,覆盖率相当于紧密堆积的多层。吸附等温线与接触角无关,表明在所有情况下疏水吸引力都克服了静电排斥力。高度结构化且刚性的吸附层显著降低聚并动力学:在或高于单层表面覆盖率时,形成稳定的液滴絮凝网络,并且无论其润湿性如何,颗粒在聚并过程中都不会从界面脱离。在亚单层纳米颗粒覆盖率下,观察到有限的聚并,并且界面饱和限制了液滴尺寸的增加。当纳米颗粒界面覆盖率>0.7且<1.0时,已注意到中间相状微观结构,其物理形式和稳定性取决于接触角。单层覆盖率且由具有不同疏水化水平的纳米颗粒混合物组成的吸附纳米颗粒层形成稳定的液滴网络,而疏水化和亲水性纳米颗粒的混合物不能有效地稳定乳液液滴。