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受限薄膜中支化聚酯的分子动力学

Molecular dynamics of hyperbranched polyesters in the confinement of thin films.

作者信息

Serghei A, Mikhailova Y, Huth H, Schick C, Eichhorn K-J, Voit B, Kremer F

机构信息

Leipzig University, Institute for Experimental Physics I, Leipzig, Germany.

出版信息

Eur Phys J E Soft Matter. 2005 Jun;17(2):199-202. doi: 10.1140/epje/i2005-10009-7. Epub 2005 May 24.

Abstract

Broadband Dielectric Spectroscopy is employed to investigate the molecular dynamics in thin films of hyperbranched polyesters (type AB(1)B(2), with -OH and -OCOCH(3) as terminal groups). Three relaxation processes are detected: alpha, beta and gamma. While the latter two are not influenced by the confinement, a pronounced effect is observed on the alpha relaxation: with decreasing film thickness the slower relaxation modes of the dynamic glass transition are gradually suppressed, resulting in an increase of the average relaxation rate and in a linear decrease of the dielectric strength. This is attributed to an immobilization in confinement of the polymeric segments located at the periphery of the hyperbranched macromolecular structures.

摘要

采用宽带介电谱研究超支化聚酯(AB(1)B(2)型,端基为-OH和-OCOCH(3))薄膜中的分子动力学。检测到三个弛豫过程:α、β和γ。后两个过程不受限制的影响,但在α弛豫上观察到显著效应:随着薄膜厚度减小,动态玻璃化转变的较慢弛豫模式逐渐受到抑制,导致平均弛豫速率增加,介电强度呈线性下降。这归因于位于超支化大分子结构外围的聚合物链段在受限环境中的固定化。

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