How brittle-ductile transition (BDT) in uniaxial compression depends on the network structure affected by predeformation
ORAL
Abstract
Polystyrene of sufficiently high molecular weight is nevertheless brittle at room temperature upon tensile extension. However, the same brittle PS is actually ductile in uniaxial compression. Our recently proposed phenomenological molecular model1 can not only explain this intriguing different from a molecular viewpoint but also anticipate how predeformation such as melt stretching shifts the BDT. Experiments are carried out to verify our theoretical predictions. Specifically, we apply melt stretching to alter the chain network structure and examine the effects of melt stretching in comparison to the predicted responses.
1. S. Q. Wang, S. W. Cheng, P. P. Lin and X. X. Li, "A phenomenological molecular model for brittle-ductile transition and yielding of polymer glasses", J. Chem. Phys. 141, 094905 (2014).
1. S. Q. Wang, S. W. Cheng, P. P. Lin and X. X. Li, "A phenomenological molecular model for brittle-ductile transition and yielding of polymer glasses", J. Chem. Phys. 141, 094905 (2014).
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Presenters
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Jianning Liu
Department of Polymer Science, University of Akron, Polymer Science, Univ of Akron
Authors
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Jianning Liu
Department of Polymer Science, University of Akron, Polymer Science, Univ of Akron
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Xiaoxiao Li
Department of Polymer Science, University of Akron
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Weiyu Wang
Department of Chemistry, University of Tennessee, Univ of Tennessee, Knoxville
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Zhichen Zhao
Department of Polymer Science, University of Akron
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Jimmy Mays
Department of Chemistry, University of Tennessee, Univ of Tennessee, Knoxville
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Shiqing Wang
Department of Polymer Science, University of Akron, Polymer Science, Univ of Akron