Synthesis and characterization of mechanically flexible and tough cellulose nanocrystals-polyacrylamide nanocomposite hydrogels

被引:118
|
作者
Yang, Jun [1 ,2 ]
Han, Chun-Rui [2 ]
Duan, Jiu-Fang [2 ]
Ma, Ming-Guo [1 ,2 ]
Zhang, Xue-Ming [1 ,2 ]
Xu, Feng [1 ,2 ]
Sun, Run-Cang [1 ,2 ]
机构
[1] Beijing Forestry Univ, Inst Biomass Chem & Technol, Beijing, Peoples R China
[2] Beijing Forestry Univ, Coll Mat Sci & Technol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogel; Nanocomposite; Cellulose nanocrystal; Polyacrylamide; Strength; STRENGTH; BEHAVIOR; GLYCOL); GEL;
D O I
10.1007/s10570-012-9841-y
中图分类号
TB3 [工程材料学]; TS [轻工业、手工业、生活服务业];
学科分类号
0805 ; 080502 ; 0822 ;
摘要
The unique combinations of hard and soft components with core/shell structures were proposed to synthesize high strength nanocomposite hydrogels. The elastomeric hydrogels containing rod-like cellulose nanocrystals (CNCs) core and polyacrylamide shell were made from aqueous solutions via free radical polymerization in the absence of chemical cross-links. The obtained hydrogels possessed greater tensile strength and elongation ratio when compared with chemically cross-linked counterparts. Oscillatory shear experiments indicated that CNCs interacted with polymer matrix via both chemical and physical interactions and contributed to the rubbery elasticity of the hydrogels. The nanocomposite hydrogels were more viscous than the chemical hydrogels, suggesting the addition of CNC led to the increase of energy dissipating and viscoelastic properties. The network structure model was proposed and it suggested that the high extensibilities and fracture stresses were related to the well-defined network structures with low cross-linking density and lack of noncovalent interactions among polymer chains, which may promote the rearrangements of network structure at high deformations.
引用
收藏
页码:227 / 237
页数:11
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