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响应性微凝胶单层与刚性胶体之间的相互作用:从软界面到硬界面。

Interactions between a responsive microgel monolayer and a rigid colloid: from soft to hard interfaces.

作者信息

Bochenek Steffen, McNamee Cathy E, Kappl Michael, Butt Hans-Juergen, Richtering Walter

机构信息

Institute of Physical Chemistry, RWTH Aachen University, Landoltweg 2, 52074 Aachen, Germany.

出版信息

Phys Chem Chem Phys. 2021 Aug 12;23(31):16754-16766. doi: 10.1039/d1cp01703a.

Abstract

Responsive poly-N-isopropylacrylamide-based microgels are commonly used as model colloids with soft repulsive interactions. It has been shown that the microgel-microgel interaction in solution can be easily adjusted by varying the environmental parameters, e.g., temperature, pH, or salt concentration. Furthermore, microgels readily adsorb to liquid-gas and liquid-liquid interfaces forming responsive foams and emulsions that can be broken on-demand. In this work, we explore the interactions between microgel monolayers at the air-water interface and a hard colloid in the water. Force-distance curves between the monolayer and a silica particle were measured with the Monolayer Particle Interaction Apparatus. The measurements were conducted at different temperatures and lateral compressions, i.e., different surface pressures. The force-distance approach curves display long-range repulsive forces below the volume phase transition temperature of the microgels. Temperature and lateral compression reduce the stiffness of the monolayer. The adhesion increases with temperature and decreases with a lateral compression of the monolayer. When compressed laterally, the interactions between the microgels are hardly affected by temperature, as the directly adsorbed microgel fractions are nearly insensitive to temperature. In contrast, our findings show that the temperature-dependent swelling of the microgel fractions in the aqueous phase strongly influences the interaction with the probe. This is explained by a change in the microgel monolayer from a soft to a hard repulsive interface.

摘要

基于聚N-异丙基丙烯酰胺的响应性微凝胶通常被用作具有软排斥相互作用的模型胶体。研究表明,通过改变环境参数,如温度、pH值或盐浓度,可以轻松调节溶液中微凝胶与微凝胶之间的相互作用。此外,微凝胶很容易吸附到气-液和液-液界面上,形成可按需破坏的响应性泡沫和乳液。在这项工作中,我们探索了空气-水界面处的微凝胶单分子层与水中硬胶体之间的相互作用。使用单分子层颗粒相互作用装置测量了单分子层与二氧化硅颗粒之间的力-距离曲线。测量在不同温度和横向压缩下进行,即不同的表面压力下进行。力-距离接近曲线在微凝胶的体积相变温度以下显示出长程排斥力。温度和横向压缩会降低单分子层的刚度。粘附力随温度升高而增加,随单分子层的横向压缩而降低。当横向压缩时,微凝胶之间的相互作用几乎不受温度影响,因为直接吸附的微凝胶部分对温度几乎不敏感。相比之下,我们的研究结果表明,水相中微凝胶部分随温度变化的溶胀强烈影响与探针的相互作用。这可以通过微凝胶单分子层从软排斥界面变为硬排斥界面来解释。

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