Strain Hardening in Startup Shear of Long-Chain Branched Polymer Solutions

被引:21
|
作者
Liu, Gengxin [1 ]
Cheng, Shiwang [1 ]
Lee, Hyojoon [2 ,3 ]
Ma, Hongwei [1 ,4 ]
Xu, Hongde [1 ,5 ]
Chang, Taihyun [2 ,3 ]
Quirk, Roderic P. [1 ]
Wang, Shi-Qing [1 ]
机构
[1] Univ Akron, Dept Polymer Sci, Maurice Morton Inst Polymer Sci & Engn, Akron, OH 44325 USA
[2] Pohang Univ Sci & Technol POSTECH, Dept Chem, Pohang 790784, South Korea
[3] Pohang Univ Sci & Technol POSTECH, Div Adv Mat Sci, Pohang 790784, South Korea
[4] Dalian Univ Technol, Sch Chem Engn, Liaoning Key Lab Polymer Sci & Engn, Dalian 116024, Peoples R China
[5] Sinopec Beijing Chem Ind Inst, Yanshan Branch, Beijing 100013, Peoples R China
基金
美国国家科学基金会;
关键词
CONVECTIVE CONSTRAINT RELEASE; ENTANGLED POLYMERS; MOLECULAR RHEOLOGY; MICROSCOPIC THEORY; COMB POLYMERS; DYNAMICS; POLYETHYLENE; SCATTERING; STRETCH; FLOWS;
D O I
10.1103/PhysRevLett.111.068302
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
We show for the first time that entangled polymeric liquids containing long-chain branching can exhibit strain hardening upon startup shear. As the significant long-chain branching impedes chain disentanglement, Gaussian coils between entanglements can deform to reach the finite extensibility limit where the intrachain retraction force exceeds the value expected from the usual conformational entropy loss evaluated based on Gaussian chain statistics. The phenomenon is expected to lead to further theoretical understanding.
引用
收藏
页数:4
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