cis-Fused cyclohexane promoted the chemical recycling of polycarbonate to monomer

被引:6
|
作者
Shan, Si-Yi [1 ]
Zhang, Wei [2 ]
Cao, Qing [1 ]
Ye, Yun-Cong [1 ]
Cai, Zhongzheng [1 ]
Zhu, Jian-Bo [1 ]
机构
[1] Sichuan Univ, Coll Chem, Natl Engn Lab Ecofriendly Polymer Mat Sichuan, Chengdu 610064, Peoples R China
[2] Tianjin Univ Sci & Technol, Coll Chem Engn & Mat Sci, Tianjin Key Lab Brine Chem Engn & Resource Ecoutil, Tianjin 300457, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
RING-OPENING POLYMERIZATION; OPPORTUNITIES; TOUGH;
D O I
10.1039/d4py00005f
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The development of chemically recyclable polymers serves as a promising strategy to solve the plastic pollution issue. In this contribution, we prepared a seven-membered cyclic carbonate with a cis-fused cyclohexane structure (C6DO). Ring-opening polymerization of this monomer afforded the aliphatic polycarbonate P(C6DO) with high molecular weight and narrow polydispersity. Copolymerization of C6DO with L-lactide (L-LA) allowed access to a series of random copolymers with various C6DO compositions. Changing the C6DO content in the copolymers led to fine-tuning of the thermal and mechanical properties of the resulting copolymers. The amorphous P(C6DO) displayed excellent ductility, with an elongation at break of 423.41 +/- 39.22%. Remarkably, copolymer P[(C6DO)(800)-co-(L-LA)(200)] demonstrated a tensile strength at break of 10.88 +/- 1.08 MPa and elongation at break of 336.78 +/- 46.13%. More importantly, P(C6DO) could be effectively and selectively depolymerized into the corresponding monomer C6DO, establishing a circular plastic economy.
引用
收藏
页码:1070 / 1076
页数:7
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