Aihua ShiXiangyi DaiZhanxin Jing
Chitosan/poly(acrylamide-co-acrylic acid) double network hydrogels based on non-covalent bond and winding between molecular chains were synthesized by copolymerization reaction in the presence of Fe3+. The formation mechanism of chitosan/poly(acrylamide-co-acrylic acid) double network hydrogels was analyzed using UV–Vis spectra and FTIR, revealing that Fe3+ could form the electrostatic interaction with –COO– group in poly(acrylamide-co-acrylic acid) chains, and the –COOH form also the hydrogen bond also with –CONH2 in poly(acrylamide-co-acrylic acid) chains or –NH2 in chitosan chains. Mechanical properties of the prepared double network hydrogels were investigated by rheological and mechanical measurements. These results indicated that the chitosan/poly(acrylamide-co-acrylic acid) double network hydrogels present good recovery ability. The tensile strength and elongation at break of the synthesized hydrogel could reach 141.9 kPa and 18.2 mm/mm, respectively, their compressive strength could reach 1.76 MPa at strain of 85%. In addition, the synthesized hydrogels can maintain good self-healing capacity owing to the dynamically reversible bonds (ionic bond and hydrogel bonding). This work provides a facile method for the synthesis of hydrogels with toughness and self-healing capacity. The synthesized chitosan/poly(acrylamide-co-acrylic acid) double network hydrogels would have a great potential applications in a diverse range.
Zhanxin JingAixing XuYan‐Qiu LiangZhaoxia ZhangChuanming YuPengzhi HongYong Li
Yu. M. SamchenkoZ. R. UlbergS. A. KomarskiiI. G. KovzunI. T. Protsenko
Issa KatimeRosa NovoaElena Díaz de ApodacaE. MendizábalJ. E. Puig
Hongwei ZhouGuohe XuJie LiShihao ZengXiaolong ZhangZhaohui ZhengXiaobin DingWeixing ChenQiguan WangWenzhi Zhang
Tingting LiXiangming HuQingsong ZhangYanyun ZhaoPeng WangXin WangBotao QinWei Lu