Vigil Daniel L, Zhang Amy, Delaney Kris T, Fredrickson Glenn H
Department of Chemical Engineering, University of California, Santa Barbara, California 93106, United States.
Materials Research Laboratory, University of California, Santa Barbara, California 93106, United States.
Macromolecules. 2023 Dec 13;56(24):9994-10005. doi: 10.1021/acs.macromol.3c01653. eCollection 2023 Dec 26.
We study a binary blend of telechelic homopolymers that can form reversible AB-type bonds at the chain ends. Reversibly bonding polymers display novel material properties, including thermal tunability and self-healing, that are not found in conventional covalently bonded polymers. Previous studies of reversibly bonding polymer systems have been limited by the computational demand of accounting for an infinite number of possible reaction products in a spatially inhomogeneous, self-assembled structure. We demonstrate that newly developed theoretical models and numerical methods enable the simultaneous computation of phase equilibrium, reaction equilibrium, and self-assembly via self-consistent field theory. Phase diagrams are computed at a variety of physically relevant conditions and are compared with nonreactive analogues as well as previous experimental studies of telechelic polymer blends.
我们研究了一种遥爪均聚物的二元共混物,其链端可形成可逆的AB型键。可逆键合聚合物展现出新型材料特性,包括热可调性和自修复性,这在传统共价键合聚合物中并未发现。先前对可逆键合聚合物体系的研究受到计算需求的限制,即在空间不均匀的自组装结构中考虑无限数量的可能反应产物。我们证明,新开发的理论模型和数值方法能够通过自洽场理论同时计算相平衡、反应平衡和自组装。在各种物理相关条件下计算相图,并与非反应类似物以及先前关于遥爪聚合物共混物的实验研究进行比较。