Thermal stiffening of hydrophobic association hydrogels

被引:12
|
作者
Owusu-Nkwantabisah, Silas [1 ]
Gillmor, Jeffrey [2 ]
Bennett, Grace [1 ]
Slater, Gary [2 ]
Szakasits, Megan [3 ]
Rajeswaran, Manju [2 ]
Antalek, Brian [2 ]
机构
[1] Eastman Kodak Co, Kodak Res Labs, 1999 Lake Ave, Rochester, NY 14650 USA
[2] Eastman Kodak Co, Tech Solut Div, 1999 Lake Ave, Rochester, NY 14650 USA
[3] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
关键词
Thermal stiffening; Self-healing hydrogel; Stimuli-responsive; DOUBLE-NETWORK HYDROGELS; MODIFIED SUPRAMOLECULAR HYDROGELS; STRUCTURAL REARRANGEMENT; TOUGH; BIOMATERIALS;
D O I
10.1016/j.polymer.2018.05.022
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Strong and tough hydrogels, important for several materials and bio-applications, typically consist of nanocomposites and double networks. There is the need to create hydrogels that exhibit tunable mechanical properties on demand without compromising other functional properties. This work demonstrates the rapid thermal stiffening of a hydrophobic association hydrogel while maintaining its optical quality and chemical composition. Up to 100-fold increase in modulus of the methacrylate-based hydrogel was achieved by an increase in temperature from 25 degrees C to 50 degrees C. Based on various characterizations, we proposed that the thermal stiffening is related to the polymer conformational changes and the ensuing increase in inter-chain hydrophobic associations at the expense of intra-chain associations. The temperature above which thermal stiffening occurs can be tuned with the polymer content in the hydrogel. Furthermore, hydrogels containing a lower mole fraction of the hydrophobic groups exhibit unusual "gel-sol-gel" transitions with temperature increase. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:374 / 381
页数:8
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