Institut des Matériaux and Institut des Sciences et Ingénierie Chimiques, Laboratoire des Polymères, École Polytechnique Fédérale de Lausanne (EPFL), Station 12, CH-1015 Lausanne, Switzerland.
Langmuir. 2023 Mar 14;39(10):3546-3557. doi: 10.1021/acs.langmuir.2c02801. Epub 2023 Feb 27.
Swelling in polymer materials is a ubiquitous phenomenon. At a molecular level, swelling is dictated by solvent-polymer interactions, and has been thoroughly studied both theoretically and experimentally. Favorable solvent-polymer interactions result in the solvation of polymer chains. For polymers in confined geometries, such as those that are tethered to surfaces, or for polymer networks, solvation can lead to swelling-induced tensions. These tensions act on polymer chains and can lead to stretching, bending, or deformation of the material both at the micro- and macroscopic scale. This Invited Feature Article sheds light on such swelling-induced mechanochemical phenomena in polymer materials across dimensions, and discusses approaches to visualize and characterize these effects.
聚合物材料的溶胀是一种普遍存在的现象。在分子水平上,溶胀取决于溶剂-聚合物相互作用,已经在理论和实验上进行了深入研究。有利的溶剂-聚合物相互作用导致聚合物链的溶剂化。对于受限几何形状的聚合物,例如那些与表面键合的聚合物,或者对于聚合物网络,溶剂化可能导致溶胀诱导的张力。这些张力作用在聚合物链上,并可能导致材料在微观和宏观尺度上的拉伸、弯曲或变形。本文特邀综述了聚合物材料在不同维度上的这种溶胀诱导的机械化学现象,并讨论了可视化和表征这些效应的方法。