Entropy-driven polymer collapse on increasing the temperature: The case of poly(N-vinylcaprolactam)

被引:0
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作者
Graziano, Giuseppe [1 ]
机构
[1] Univ Sannio, Dept Sci & Technol, Via Francesco de Sanctis Snc, I-82100 Benevento, Italy
关键词
Endothermic polymer collapse; Entropic driving force; Work of cavity creation; Solvent -excluded volume effect; Small size of water molecules; TO-GLOBULE TRANSITION; SCALED PARTICLE THEORY; CAVITY SIZE DISTRIBUTION; SOLVATION FREE-ENERGY; AQUEOUS-SOLUTIONS; CHAIN COLLAPSE; THERMORESPONSIVE POLYMERS; HYDROPHOBIC INTERACTION; STRUCTURAL ORDER; NONPOLAR SOLUTES;
D O I
10.1016/j.molliq.2024.124509
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Poly(N-vinylcaprolactam), PNVCL, chains undergo a temperature-induced, reversible and endothermic collapse in water at around 32 degrees C. The entropy gain driving PNVCL collapse has to come from water molecules, but it cannot be associated with their passage from the polymer hydration shell to the bulk because there is no difference in their tetrahedral structural order. I have shown that the water entropy gain comes from the decrease in solvent-excluded volume effect associated with chain collapse: there is a marked increase in the spatial configurations accessible to water molecules, leading to a large gain in their translational entropy. This mechanism, even though generic, proves to be effective solely in water and aqueous solutions because the magnitude of the solvent-excluded volume effect is amplified by the large number density of water, stemming from the strength of H-bonds and the small size of water molecules.
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页数:8
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