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Self-healable, tough and highly stretchable ionic nanocomposite physical hydrogels
被引:149
|作者:
Zhong, Ming
[1
]
Liu, Xiao-Ying
[1
]
Shi, Fu-Kuan
[1
]
Zhang, Li-Qin
[1
]
Wang, Xi-Ping
[1
]
Cheetham, Andrew G.
[2
,3
]
Cui, Honggang
[2
,3
]
Xie, Xu-Ming
[1
]
机构:
[1] Tsinghua Univ, Dept Chem Engn, Lab Adv Mat MOE, Beijing 100084, Peoples R China
[2] Johns Hopkins Univ, Dept Biomol & Chem Engn, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Inst NanoBioTechnol, Baltimore, MD 21218 USA
来源:
关键词:
DOUBLE-NETWORK HYDROGELS;
HIGH MECHANICAL STRENGTH;
CROSS-LINKING;
DESIGN;
CLAY;
POLYMER;
GEL;
D O I:
10.1039/c5sm00493d
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:
We present a facile strategy to synthesize self-healable tough and highly stretchable hydrogels. Our design rationale for the creation of ionic cross-linked hydrogels is to graft an acrylic acid monomer on the surface of vinyl hybrid silica nanoparticles (VSNPs) for the growth of poly(acrylic) acid (PAA), and the obtained VSNP-PAA nanobrush can be used as a gelator. Physical cross-linking through hydrogen bonding and ferric ion-mediated ionic interactions between PAA polymer chains of the gelators yielded ionic nanocomposite physical hydrogels with excellent and balanced mechanical properties (tensile strength 860 kPa, elongation at break similar to 2300%), and the ability to self-repair (tensile strength similar to 560 kPa, elongation at break similar to 1800%). The toughness and stretchability arise from the reversible cross-linking interactions between the polymer chains that help dissipate energy through stress (deformation) triggered dynamic processes. These unique properties will enable greater application of these hydrogel materials, especially in tissue engineering.
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页码:4235 / 4241
页数:7
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