Swelling thermodynamics and phase transitions of polymer gels

被引:31
作者
Dimitriyev, Michael S. [1 ]
Chang, Ya-Wen [2 ]
Goldbart, Paul M. [3 ]
Fernandez-Nieves, Alberto [1 ,4 ,5 ]
机构
[1] Georgia Inst Technol, Sch Phys, Atlanta, GA 30332 USA
[2] Texas Tech Univ, Dept Chem Engn, Lubbock, TX 79409 USA
[3] Univ Texas Austin, Dept Phys, Austin, TX 78712 USA
[4] Univ Barcelona, Dept Condensed Matter Phys, E-08028 Barcelona, Spain
[5] ICREA, Barcelona 08010, Spain
关键词
polymer gels; phase transitions; phase coexistence; extreme thermodynamics; toroidal hydrogels; swelling and deswelling; thermoresponsive materials; PATTERN-FORMATION; STATISTICAL-MECHANICS; DRUG-DELIVERY; BULK MODULUS; SURFACE; INSTABILITY; HYDROGELS; NETWORKS; COEXISTENCE; HYSTERESIS;
D O I
10.1088/2399-1984/ab45d5
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We present a pedagogical review of the swelling thermodynamics and phase transitions of polymer gels. In particular, we discuss how features of the volume phase transition of the gel's osmotic equilibrium are analogous to other transitions described by mean-field models of binary mixtures, and the failure of this analogy at the critical point due to shear rigidity. We then consider the phase transition at fixed volume, a relatively unexplored paradigm for polymer gels that results in a phase-separated equilibrium consisting of coexisting solvent-rich and solvent-poor regions of gel. Again, the gel's shear rigidity is found to have a profound effect on the phase transition, here resulting in macroscopic shape change at constant volume of the sample, exemplified by the tunable buckling of toroidal samples of polymer gel. By drawing analogies with extreme mechanics, where large shape changes are achieved via mechanical instabilities, we formulate the notion of extreme thermodynamics, where large shape changes are achieved via thermodynamic instabilities, i.e. phase transitions.
引用
收藏
页码:1 / 43
页数:43
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