Department of Chemical Engineering, University of Waterloo , 200 University Avenue West, Waterloo, Ontario N2L 3G1, Canada.
Langmuir. 2017 Oct 10;33(40):10568-10576. doi: 10.1021/acs.langmuir.7b02051. Epub 2017 Sep 26.
Pickering emulsions stabilized by nanoparticles have recently received great attention for their remarkable stability, in part a consequence of irreversible adsorption. In this study, we generate Pickering oil-in-water emulsions stabilized by ethyl cellulose (EC) nanoparticles without the addition of surfactants. Over a range of ionic strength and EC nanoparticle concentrations, a series of dynamic interfacial tension (IFT) measurements complemented by extended DLVO theoretical computations are conducted to quantitatively describe the behavior of EC nanoparticles at the interface of water with different alkanes. Regardless of ionic strength, there is no barrier against the adsorption of EC nanoparticles at the alkane-water interfaces studied and the particles tightly cover these interfaces with near maximal coverage (i.e., 91%). Remarkably, the rate of approach to maximum coverage of the alkane-water interface by EC nanoparticles during the later stages of adsorption is accelerated in the presence of salt at concentrations below the critical coagulation concentration (CCC), unlike the air-water interface. Above the CCC, alkane-water interfaces behave similar to air-water interfaces, showing decay in the adsorption flux which is attributed to an increase in surface blocking originating from the attachment of nanoparticles to nanoparticles already adsorbed at the interface. These findings shed light on particle-particle and particle-interface colloidal interactions at and near fluid-fluid interfaces, thereby improving our ability to use hydrophobic EC nanoparticles as emulsion stabilizers.
由纳米颗粒稳定的 Pickering 乳液因其显著的稳定性而受到广泛关注,部分原因是不可逆吸附。在这项研究中,我们生成了由乙基纤维素(EC)纳米颗粒稳定的 Pickering 水包油乳液,无需添加表面活性剂。在一系列离子强度和 EC 纳米颗粒浓度范围内,进行了一系列动态界面张力(IFT)测量,并辅以扩展的 DLVO 理论计算,以定量描述 EC 纳米颗粒在不同烷烃与水界面的行为。无论离子强度如何,在所研究的烷烃-水界面上,EC 纳米颗粒的吸附都没有障碍,颗粒紧密覆盖这些界面,接近最大覆盖率(即 91%)。值得注意的是,在低于临界聚沉浓度(CCC)的盐浓度下,EC 纳米颗粒在吸附后期达到最大覆盖烷烃-水界面的速率会加快,这与空气-水界面不同。在 CCC 以上,烷烃-水界面的行为类似于空气-水界面,吸附通量衰减,这归因于表面阻塞的增加,这是由于已经吸附在界面上的纳米颗粒之间的相互作用导致的。这些发现揭示了在流体-流体界面处和附近的颗粒-颗粒和颗粒-界面胶体相互作用,从而提高了我们使用疏水性 EC 纳米颗粒作为乳液稳定剂的能力。