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二嵌段共聚物熔体的弗兰克-卡斯珀相:两种常用模型的自洽场结果

Frank-Kasper Phases of Diblock Copolymer Melts: Self-Consistent Field Results of Two Commonly Used Models.

作者信息

He Juntong, Wang Qiang

机构信息

Department of Chemical and Biological Engineering, Colorado State University, 1370 Campus Delivery, Fort Collins, CO 80523, USA.

出版信息

Polymers (Basel). 2024 Jan 29;16(3):372. doi: 10.3390/polym16030372.

DOI:10.3390/polym16030372
PMID:38337261
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10857353/
Abstract

We constructed phase diagrams of conformationally asymmetric diblock copolymer A-B melts using the polymer self-consistent field (SCF) calculations of both the dissipative particle dynamics chain (DPDC) model (i.e., compressible melts of discrete Gaussian chains with the DPD non-bonded potential) and the "standard" model (i.e., incompressible melts of continuous Gaussian chains with the Dirac -function non-bonded potential) in the - plane, where and characterize, respectively, the repulsion and conformational asymmetry between the A and B blocks, at the A-block volume fraction = 0.2 and 0.3. Consistent with previous SCF calculations of the "standard" model, σ and A15 are the only stable Frank-Kasper (FK) phases among the five FK (i.e., σ, A15, C14, C15 and Z) phases considered. The stability of σ and A15 is due to their delicate balance between the energetic and entropic contributions to the Helmholtz free energy per chain of the system, which, within our parameter range, increases in the order of σ/A15, Z, and C14/C15. While in general the SCF phase diagrams of these two models are qualitatively consistent, A15 is not stable for the DPDC model at the copolymer chain length = 10 and = 0.3; any differences in the SCF phase diagrams are solely due to the differences between these two models.

摘要

我们使用耗散粒子动力学链(DPDC)模型(即具有DPD非键合势的离散高斯链的可压缩熔体)和“标准”模型(即具有狄拉克函数非键合势的连续高斯链的不可压缩熔体)的聚合物自洽场(SCF)计算,构建了构象不对称二嵌段共聚物A - B熔体在(\sigma - A_{15})平面中的相图,其中(\sigma)和(A_{15})分别表征A和B嵌段之间的排斥和构象不对称,A嵌段体积分数(\phi_A = 0.2)和(0.3)。与先前对“标准”模型的SCF计算一致,在考虑的五个Frank - Kasper(FK)相(即(\sigma)、(A_{15})、(C_{14})、(C_{15})和Z)中,(\sigma)和(A_{15})是仅有的稳定相。(\sigma)和(A_{15})的稳定性源于它们对系统每条链的亥姆霍兹自由能的能量和熵贡献之间的微妙平衡,在我们的参数范围内,这种平衡按(\sigma / A_{15})、Z和(C_{14} / C_{15})的顺序增加。虽然一般来说这两个模型的SCF相图在定性上是一致的,但对于DPDC模型,在共聚物链长(N = 10)和(\phi_A = 0.3)时(A_{15})不稳定;SCF相图中的任何差异完全是由于这两个模型之间的差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1000/10857353/3dedc0f82018/polymers-16-00372-g006a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1000/10857353/f8fd3e58781b/polymers-16-00372-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1000/10857353/7a0dd46f8c33/polymers-16-00372-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1000/10857353/95938bfefd34/polymers-16-00372-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1000/10857353/6895a95b1824/polymers-16-00372-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1000/10857353/6559c47cbf6c/polymers-16-00372-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1000/10857353/3dedc0f82018/polymers-16-00372-g006a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1000/10857353/f8fd3e58781b/polymers-16-00372-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1000/10857353/7a0dd46f8c33/polymers-16-00372-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1000/10857353/95938bfefd34/polymers-16-00372-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1000/10857353/6895a95b1824/polymers-16-00372-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1000/10857353/6559c47cbf6c/polymers-16-00372-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1000/10857353/3dedc0f82018/polymers-16-00372-g006a.jpg

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本文引用的文献

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