Yang Diling, Xie Lei, Mao Xiaohui, Gong Lu, Peng Xuwen, Peng Qiongyao, Wang Tao, Liu Qi, Zeng Hongbo, Zhang Hao
Department of Chemical and Materials Engineering, University of Alberta, Edmonton, Alberta T6G 1H9, Canada.
Langmuir. 2022 May 3;38(17):5257-5268. doi: 10.1021/acs.langmuir.1c02635. Epub 2021 Nov 17.
Hydrophobic interaction plays an important role in numerous interfacial phenomena and biophysical and industrial processes. In this work, polystyrene (PS) was used as a model hydrophobic polymer for investigating its hydrophobic interaction with highly deformable objects (i.e., air bubbles and oil droplets) in aqueous solutions. The effects of polymer molecular weight, solvent (i.e., addition of ethanol to water), the presence of surface-active species, and hydrodynamic conditions were investigated, via direct surface force measurements using the bubble/drop probe atomic force microscopy (AFM) technique and theoretical calculations based on the Reynolds lubrication theory and augmented Young-Laplace equation by including the effect of disjoining pressure. It was found that the PS of low molecular weight (i.e., PS590 and PS810) showed slightly weaker hydrophobic interactions with air bubbles or oil droplets, as compared to glassy PS of higher molecular weight (i.e., PS1110, PS2330, PS46300, and PS1M). The hydrophobic interaction between PS and air bubbles in a 1 M NaCl aqueous solution with 10 vol % ethanol was weaker than that in the bare aqueous solution. Such effects on the hydrophobic interactions are possibly achieved by influencing the structuring/ordering of water molecules close to the hydrophobic polymer surfaces by tuning the surface chain mobility and surface roughness of polymers. It was found that the addition of three surface-active species, i.e., cetyltrimethylammonium chloride (CTAC), Pluronic F-127, and sodium dodecyl sulfate (SDS), to the aqueous media could suppress the attachment of the hydrophobic polymer and air bubbles or oil droplets, most likely caused by the additional steric repulsion due to the adsorbed surface-active species at the bubble/polymer/oil interfaces. Our results have improved the fundamental understanding of the interaction mechanisms between hydrophobic polymers and gas bubbles or oil droplets, with useful implications on developing effective methods for modulating the related interfacial interactions in many engineering applications.
疏水相互作用在众多界面现象以及生物物理和工业过程中起着重要作用。在这项工作中,聚苯乙烯(PS)被用作模型疏水聚合物,以研究其在水溶液中与高度可变形物体(即气泡和油滴)的疏水相互作用。通过使用气泡/液滴探针原子力显微镜(AFM)技术进行直接表面力测量以及基于雷诺润滑理论和通过纳入分离压力效应的扩展杨-拉普拉斯方程进行理论计算,研究了聚合物分子量、溶剂(即向水中添加乙醇)、表面活性物质的存在以及流体动力学条件的影响。结果发现,与较高分子量的玻璃态PS(即PS1110、PS2330、PS46300和PS1M)相比,低分子量的PS(即PS590和PS810)与气泡或油滴的疏水相互作用稍弱。在含有10体积%乙醇的1 M NaCl水溶液中,PS与气泡之间的疏水相互作用比在纯水溶液中弱。对疏水相互作用的这种影响可能是通过调节聚合物的表面链流动性和表面粗糙度来影响靠近疏水聚合物表面的水分子的结构/有序性而实现的。研究发现,向水介质中添加三种表面活性物质,即十六烷基三甲基氯化铵(CTAC)、普朗尼克F-127和十二烷基硫酸钠(SDS),可以抑制疏水聚合物与气泡或油滴的附着,这很可能是由于在气泡/聚合物/油界面处吸附的表面活性物质产生的额外空间排斥作用所致。我们的结果增进了对疏水聚合物与气泡或油滴之间相互作用机制的基本理解,对开发有效方法来调节许多工程应用中的相关界面相互作用具有重要意义。