Biobased Dynamic Polymer Networks with Rapid Stress Relaxation

被引:55
作者
Zhao, Shizhen [1 ,2 ]
Wang, Dong [1 ,2 ]
Russell, Thomas P. [3 ,4 ]
机构
[1] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[3] Univ Massachusetts, Polymer Sci & Engn Dept, Amherst, MA 01003 USA
[4] Lawrence Berkeley Natl Lab, Mat Sci Div, Berkeley, CA 94720 USA
基金
中国国家自然科学基金;
关键词
dynamic polymer networks; epoxidized soybean oil; hydroxyl-functionalized silica; stress relaxation; mechanical properties; EPOXIDIZED SOYBEAN OIL; MECHANICAL-PROPERTIES; EPOXY VITRIMERS; CROSS-LINKING; TRANSESTERIFICATION; TEMPERATURE; FACILE; ROBUST;
D O I
10.1021/acssuschemeng.1c02826
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dynamic polymer networks (DPNs) from epoxidized soybean oil (ESO) that incorporate dual dynamic exchange reactions (dual-DERs) and hydroxyl-functionalized silica (HO-SiO2) reinforcement are shown to exhibit rapid stress relaxation and excellent mechanical properties. A disulfide-containing carboxylic acid was used to synthesize the ESO DPNs by simultaneous disulfide metathesis and transesterification reactions that are found to markedly increase the rate of stress relaxation of the networks. HO-SiO2 was used to enhance the mechanical properties while further increasing the rate of stress relaxation. Optimal performance of the ESO/SiO2 DPNs was found at a 3 wt % HO-SiO2 content. In comparison with the neat ESO DPNs, the characteristic stress relaxation time (tau*) of the ESO/SiO2-3 DPNs decreased from 1494 to 898 s at 170 degrees C. The tensile strength and elongation at break, on the other hand, increased by 150 and 113%, respectively. ESO/SiO2-3 DPNs also show excellent self-healing, welding, and recycling properties that are desirable for reuse.
引用
收藏
页码:11091 / 11099
页数:9
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