共 44 条
Structure optimization of self-healing hydrogels formed via hydrophobic interactions
被引:196
作者:
Tuncaboylu, Deniz C.
[2
]
Argun, Aslihan
[1
]
Sahin, Melahat
[1
]
Sari, Murat
[1
]
Okay, Oguz
[1
]
机构:
[1] Istanbul Tech Univ, Dept Chem, TR-34469 Istanbul, Turkey
[2] Bezmialem Univ, Fac Pharm, TR-34093 Istanbul, Turkey
来源:
关键词:
self-healing;
Hydrogels;
Hydrophobic associations;
MULTISTICKER ASSOCIATIVE POLYELECTROLYTES;
LARGE-STRAIN;
MODIFIED POLYACRYLAMIDES;
RHEOLOGICAL PROPERTIES;
AQUEOUS-SOLUTIONS;
CROSS-LINKS;
BEHAVIOR;
FRACTURE;
NETWORK;
TOUGH;
D O I:
10.1016/j.polymer.2012.10.015
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
In an attempt to mimic self-healing functions in biological systems, we investigate here the optimum design parameters of self-healing hydrogels formed by hydrophobic associations in aqueous solutions of wormlike sodium dodecyl sulfate (SDS) micelles. n-alkyl (meth)acrylates were used as the hydrophobic comonomer (2 mol %) of acrylamide in the gel preparation. Two structural parameters are crucial for obtaining self-healing gels via hydrophobic interactions. One is the length of the alkyl side chain of the hydrophobe, and the other is the surfactant concentration. In addition, hydrophobic methacrylates generate gels with a higher healing efficiency than the corresponding acrylates due to the limited flexibility of the methacrylate backbones, leading to a greater number of non-associated hydrophobic blocks. These free blocks locating near the fracture surface of the gel samples link each other to self-heal the broken hydrogel. The physical gels without SDS are very tough due to their sacrificial bonds that are broken under force and preventing the fracture of the molecular backbone. (C) 2012 Elsevier Ltd. All rights reserved.
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页码:5513 / 5522
页数:10
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