Alsmaeil Ahmed Wasel, Kouloumpis Antonios, Potsi Georgia, Hammami Mohamed Amen, Kanj Mazen Yousef, Giannelis Emmanuel P
Robert Frederick Smith School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York 14850, United States.
EXPEC Advanced Research Center, Saudi Aramco, Dhahran 31261, Saudi Arabia.
Langmuir. 2023 Feb 28;39(8):3118-3130. doi: 10.1021/acs.langmuir.2c03286. Epub 2023 Feb 15.
Particle-stabilized emulsions (Pickering emulsions) have recently attracted significant attention in scientific studies and for technological applications. The interest stems from the ease of directly assembling the particles at interfaces and modulating the interfacial properties. In this paper, we demonstrate the formation of stable, practical emulsions leveraging the assembly of ionizable, pH responsive silica nanoparticles, surface-functionalized by a mixture of silanes containing amine/ammonium groups, which renders them positively charged. Using pH as the trigger, the assembly and the behavior of the emulsion are controlled by modulating the charges of the functional groups of the nanoparticle and the oil (crude oil). In addition to their tunable charge, the particular combination of silane coupling agents leads to stable particle dispersions, which is critical for practical applications. Atomic force microscopy and interfacial tension (IFT) measurements are used to monitor the assembly, which is controlled by both the electrostatic interactions between the particles and oil and the interparticle interactions, both of which are modulated by pH. Under acidic conditions, when the surfaces of the oil and the nanoparticles (NPs) are positively charged, the NPs are not attracted at the interface and there is no significant reduction in the IFT. In contrast, under basic conditions in which the oil carries a high negative charge and the amine groups on the silica are deprotonated while still positively charged because of the ammonium groups, the NPs assemble at the interface in a closely packed configuration yielding a jammed state with a high dilatational modulus. As a result, two oil droplets do not coalesce even when pushed against each other and the emulsion stability improves significantly. The study provides new insights into the directed assembly of nanoparticles at fluid interfaces relevant to several applications, including environmental remediation, catalysis, drug delivery, food technology, and oil recovery.
颗粒稳定乳液(皮克林乳液)最近在科学研究和技术应用中引起了广泛关注。这种兴趣源于在界面处直接组装颗粒并调节界面性质的简便性。在本文中,我们展示了利用可电离的、pH响应性二氧化硅纳米颗粒的组装形成稳定、实用的乳液,这些纳米颗粒通过含有胺/铵基团的硅烷混合物进行表面功能化,使其带正电荷。以pH为触发因素,通过调节纳米颗粒和油(原油)官能团的电荷来控制乳液的组装和行为。除了其可调节的电荷外,硅烷偶联剂的特定组合导致稳定的颗粒分散体,这对于实际应用至关重要。使用原子力显微镜和界面张力(IFT)测量来监测组装过程,该过程由颗粒与油之间的静电相互作用以及颗粒间相互作用共同控制,而这两种相互作用均受pH调节。在酸性条件下,当油和纳米颗粒(NPs)表面带正电荷时,NPs不会在界面处被吸引,IFT也没有显著降低。相反,在碱性条件下,油带高负电荷,二氧化硅上的胺基团去质子化,同时由于铵基团仍带正电荷,NPs以紧密堆积的构型组装在界面处,形成具有高膨胀模量的堵塞状态。结果,即使两个油滴相互挤压也不会聚结,乳液稳定性显著提高。该研究为纳米颗粒在与多种应用相关的流体界面上的定向组装提供了新的见解,这些应用包括环境修复、催化、药物递送、食品技术和石油开采。