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全生物可降解聚(L-乳酸)/聚(D-乳酸)-聚(丙交酯-己内酯)嵌段聚合物薄膜的构建:粘弹性、加工性能和柔韧性。

Construction of fully biodegradable poly(L-lactic acid)/poly(D-lactic acid)-poly(lactide-co-caprolactone) block polymer films: Viscoelasticity, processability and flexibility.

作者信息

He Wenjun, Ye Lin, Coates Phil, Caton-Rose Fin, Zhao Xiaowen

机构信息

State Key Laboratory of Polymer Materials Engineering, Polymer Research Institute of Sichuan University, Chengdu 610065, China.

School of Engineering, Design and Technology, University of Bradford, Bradford, UK.

出版信息

Int J Biol Macromol. 2023 May 1;236:123980. doi: 10.1016/j.ijbiomac.2023.123980. Epub 2023 Mar 9.

Abstract

Development of biodegradable polymer films is essential for sustainable energy conservation and ecological protection. In this work, to improve the processability and toughness of poly(lactic acid) (PLA) films, poly(lactide-co-caprolactone) (PLCL) segments were introduced into poly(L-lactic acid) (PLLA)/poly(D-lactic acid) (PDLA) chains via chain branching reactions during reactive processing, and fully biodegradable/flexible PLLA/D-PLCL block polymer with long-chain branches and stereocomplex (SC) crystalline structure was prepared. Compared with neat PLLA, PLLA/D-PLCL exhibited much higher complex viscosity/storage modulus, lower tanδ values in terminal region and obvious strain-hardening behavior. Through biaxial drawing, PLLA/D-PLCL films were prepared, which showed improved uniformity and non-preferred orientation. With increasing draw ratio, the total crystallinity (X) and X for SC crystal both increased. By introduction of PDLA, the two phases of PLLA and PLCL penetrated and entangled with each other, and the phase structure transformed from "sea-island" structure to "co-continuous network" structure, which was beneficial for exerting the toughening effect of flexible PLCL molecules on PLA matrix. The tensile strength and elongation at break of PLLA/D-PLCL films increased from 51.87 MPa and 28.22 % of neat PLLA film to 70.82 MPa and 148.28 %. This work provided a new strategy for developing fully biodegradable polymer films with high performance.

摘要

可生物降解聚合物薄膜的开发对于可持续能源节约和生态保护至关重要。在这项工作中,为了提高聚乳酸(PLA)薄膜的加工性能和韧性,通过反应加工过程中的链支化反应将聚(丙交酯 - 共 - 己内酯)(PLCL)链段引入聚(L - 乳酸)(PLLA)/聚(D - 乳酸)(PDLA)链中,制备了具有长链支化和立体复合(SC)晶体结构的完全可生物降解/柔性PLLA / D - PLCL嵌段聚合物。与纯PLLA相比,PLLA / D - PLCL表现出更高的复数粘度/储能模量,在末端区域具有更低的tanδ值以及明显的应变硬化行为。通过双轴拉伸制备了PLLA / D - PLCL薄膜,其均匀性和非择优取向得到改善。随着拉伸比的增加,总结晶度(X)和SC晶体的X均增加。通过引入PDLA,PLLA和PLCL的两相相互渗透并缠结,相结构从“海岛”结构转变为“共连续网络”结构,这有利于发挥柔性PLCL分子对PLA基体的增韧作用。PLLA / D - PLCL薄膜的拉伸强度和断裂伸长率从纯PLLA薄膜的51.87MPa和28.22%提高到70.82MPa和148.28%。这项工作为开发高性能的完全可生物降解聚合物薄膜提供了一种新策略。

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