Associating Polymers in the Strong Interaction Regime: Validation of the Bond Lifetime Renormalization Model

被引:7
|
作者
Ge, Sirui [1 ]
Carden, Gregory Peyton [2 ]
Samanta, Subarna [2 ]
Li, Bingrui [3 ]
Popov, Ivan [2 ]
Cao, Peng-Fei [4 ]
Sokolov, Alexei P. [2 ,5 ]
机构
[1] Univ Tennessee, Dept Mat Sci & Engn, Knoxville, TN 37996 USA
[2] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
[3] Univ Tennessee, Bredesen Ctr Interdisciplinary Res & Grad Educ, Knoxville, TN 37996 USA
[4] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[5] Oak Ridge Natl Lab, Chem Sci Div, Oak Ridge, TN 37830 USA
基金
美国国家科学基金会;
关键词
DYNAMICS; CHAIN; RELAXATION; NETWORKS; DESIGN;
D O I
10.1021/acs.macromol.2c02446
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Quantitative understanding of dynamics and viscoelastic properties of associating polymers remains a challenge. This study presents detailed analysis of dielectric and rheological data for telechelic PDMS functionalized with two different end groups, urea that forms multiple hydrogen bonds and carboxylic acid that forms much weaker hydrogen bonds. Analysis of the results revealed that the bond dissociation and bond rearrangement times are similar in the case of strong bonding urea-functionalized samples but are different in the case of weaker interacting carboxylic acid end groups. We demonstrate that these results agree well with the predictions of the bond lifetime renormalization model. The presented results suggest that rheological data can be used for the estimation of activation energy for bond dissociation only in the strong interaction regime and that segmental relaxation should be explicitly accounted for in these estimates, at least, in the systems studied herein.
引用
收藏
页码:2397 / 2405
页数:9
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