Multi-responsive, tough and reversible hydrogels with tunable swelling property

被引:37
|
作者
Zhang, Man [1 ]
Wang, Rui [1 ]
Shi, Zhenqiang [1 ]
Huang, Xuelian [1 ]
Zhao, Weifeng [1 ,2 ]
Zhao, Changsheng [1 ]
机构
[1] Sichuan Univ, Coll Polymer Sci & Engn, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
[2] Royal Inst Technol KTH, Fiber & Polymer Technol, Sch Chem Sci & Engn, Teknikringen 56-58, SE-10044 Stockholm, Sweden
基金
中国国家自然科学基金;
关键词
Multi-responsiveness; Reversibility; Slightly chemical cross-linking; Environmental pollution remediation; HEMICELLULOSE HYDROGELS; CATALYTIC-REDUCTION; CONTROLLED-RELEASE; CROSS-LINKING; PH; DYE;
D O I
10.1016/j.jhazmat.2016.10.016
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A novel family of multi-responsive, tough, and reversible hydrogels were prepared by the combination of dipole-dipole interaction, hydrogen bonding interaction and slightly chemical cross-linking, using monomers of acrylonitrile, sodium allylsulfonate and itaconic acid. Reversible gel-sol transition was achieved by the flexible conversion of the dipole-dipole interactions between acrylonitrile-acrylonitrile and acrylonitrile-sodium thiocyanate, and the hydrogels could freely form desired shapes. The dipole dipole and hydrogen bonding interactions improved the mechanical strength of the hydrogels with a compressive stress of 2.38 MPa. Meanwhile, the hydrogels sustained cyclic compressive tests with 60% strain, and exhibited excellent elastic property. The hydrogels were sensitive to pH and ionic strength, and could keep their perfect spherical structures without any obvious cracks even after immersing in strong ionic strength (or pH) solution for several reversible cycles. Furthermore, the hydrogels were recycled for environmental pollution remediation, and showed great potential to be applied in water treatments and other related fields. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:499 / 507
页数:9
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