Polymers with autonomous self-healing ability and remarkable reprocessability under ambient humidity conditions

被引:95
作者
Kim, Chaehoon [1 ]
Ejima, Hirotaka [2 ]
Yoshie, Naoko [1 ]
机构
[1] Univ Tokyo, Inst Ind Sci, Meguro Ku, 4-6-1 Komaba, Tokyo 1538505, Japan
[2] Univ Tokyo, Dept Mat Engn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
关键词
BORONIC ACIDS; TEMPERATURE; NETWORKS; DISULFIDE; CHEMISTRY; HYDROGEL; SACCHARIDES; COMPOSITE; MECHANISM; DESIGN;
D O I
10.1039/c8ta04769c
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
The use of moisture in self-healing polymeric materials is a very attractive option given the practical environments in which the materials are used. Herein, we incorporated tetrahedral boronate-esters bearing B-N dative bonds as dynamic crosslinks into polymers, which led to moisture-induced self-healing abilities in their bulk states. Owing to the higher rate of ester formation over tetrahedral boronate-ester hydrolysis under wet conditions, these polymers invariably maintain a sufficient number of dynamic crosslinks to facilitate a combination of autonomous healing behavior and mechanical strength, which makes them unique compared to other previously developed water-triggered self-healing polymers. The self-healed materials maintain good mechanical properties, with fracture stresses of approximate to 2 MPa, and ageing of the cut surfaces does not affect their healing efficiency. Furthermore, the tetrahedral boronate-ester bonds exhibit dual stimuli-responsive dynamic behavior triggered by either moisture or heat, resulting in network polymers with remarkable reprocessabilities.
引用
收藏
页码:19643 / 19652
页数:10
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