Tailoring vinylogous urethane chemistry for the cross-linked polybutadiene: Wide freedom design, multiple recycling methods, good shape memory behavior

被引:53
作者
Liu, Zhiyong [1 ]
Zhang, Changxu [1 ]
Shi, Zixing [1 ]
Yin, Jie [1 ]
Tian, Ming [2 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Key Lab Elect Insulat & Thermal Ageing, State Key Lab Met Matrix Composite Mat, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
[2] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
基金
上海市自然科学基金;
关键词
Vitrimer; Polybutadiene; Transamination; POLYMER NETWORKS; DYNAMIC EXCHANGE; THIOL-ENE; REORGANIZATION; POLYURETHANE; DERIVATIVES; ENAMINONES; ELASTOMER; LINKING;
D O I
10.1016/j.polymer.2018.06.042
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Vinylogous urethane chemistry can provide the sustainable way to address the demands for reprocessing the cross-linked polymers. In this paper, we extended this method to prepare the existing commercially available cross-linked polybutadiene (PB) with multiple reprocessing ways. We firstly attach acetoacetyl group to the chains of PB and then use diamines as cross-linkers to form vinylogous urethanes involved network, which could be tailored with great freedom, including via the content of attached acetoacetyl group, the ratio of amine to acetoacetyl group and different types of amine. Furthermore, the dynamic nature of the cross-linked PB is studied by stress relaxation. Based on the Arrhenius equation, the activation energy for chain re-arrangement is calculated about 48 +/- 5 kj mol(-1) and the network could be efficiently reshuffled at the temperature between 120 degrees C and 150 degrees C. More important, the cross-linked PB could be effectively remolded by hot pressing or solvent assisted welding methods via catalyst-free transamination of vinylogous urethanes. We envisage that this strategy may provide an eco-environmental method to dispose the waste rubbers and prolong their life time. (C) 2018 Published by Elsevier Ltd.
引用
收藏
页码:202 / 210
页数:9
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