Stress-Structure Relationship of the Reversible Associating Polymer Network under Start-up Shear Flow

被引:3
|
作者
Liu, Ai-Qing [1 ,2 ]
Liu, Li-Jun [2 ]
Xu, Wen-Sheng [2 ]
Xu, Xiao-Lei [2 ]
Chen, Ji-Zhong [2 ]
An, Li-Jia [2 ,3 ]
机构
[1] Jilin Univ, Coll Chem, Changchun 130012, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
[3] Univ Sci & Technol China, Hefei 230026, Peoples R China
基金
中国国家自然科学基金;
关键词
Associating polymer; Start-up shear; Stress-structure relationship; MOLECULAR-DYNAMICS SIMULATION; VISCOELASTIC PROPERTIES; TRIBLOCK COPOLYMER; CHAIN FLEXIBILITY; RHEOLOGY; GELS; GELATION; BEHAVIOR; EQUILIBRIUM; OVERSHOOT;
D O I
10.1007/s10118-020-2487-6
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We adopt Langevin dynamics to explore the stress-structure relationship of telechelic reversible associating polymer gel during startup shear flow, with shear strengths varying fromW(i)= 12.6 toW(i)= 12640. At weak shear flowW(i)= 12.6, the shear stress proportionally increases with shear strain at short times, followed by a strain hardening behavior and then passes through a maximum (sigma(max),gamma(max)) and finally decreases until it reaches the steady state. During the evolution of stress, the gel network is only slightly broken and essentially maintains its framework, and the strain hardening behavior originates from the excessive stretching of chains. On the other hand, the stress-strain curve at intermediate shear flowW(i)= 505.6 shows two differences from that atW(i)= 12.6, namely, the absence of strain hardening and a dramatic increase of stress at large strains, which is caused by the rupture of gel network at small strains and the network recovery at large strains, respectively. Finally, at very strong shear flowW(i)= 6319.7, the gel network is immediately broken by shear flow and the stress-strain curve exhibits similar behaviors to those of classical polymeric liquids.
引用
收藏
页码:387 / 396
页数:10
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