Simulations of Startup Planar Elongation of an Entangled Polymer Melt
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- Takeda Keiko
- Graduate School of Organic Materials Science, Yamagata University
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- Masubuchi Yuichi
- Department of Materials Physics, Nagoya University
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- Sugimoto Masataka
- Graduate School of Organic Materials Science, Yamagata University
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- Koyama Kiyohito
- Graduate School of Organic Materials Science, Yamagata University
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- Sukumaran Sathish K.
- Graduate School of Organic Materials Science, Yamagata University
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説明
<p>Using the primitive chain network model, we have simulated the startup of steady planar elongation of a moderately entangled polymer melt at several elongation rates. The time dependence of the first normal stress growth coefficient, η+p1, was similar to that under startup uniaxial elongation, η+u, and exhibited significant strain hardening when the Rouse Weissenberg number, WiR<tt> ≳ </tt>1. Analysis of the chain conformation revealed that planar elongation resulted in the loss of fewer entanglements and in a lower orientation anisotropy compared to uniaxial elongation, and these two effects nearly compensated each other resulting in the qualitative similarity between η+p1 and η+u. The second normal stress growth coefficient, η+p2, showed only strain softening and resembled startup shear including the appearance of a stress maximum. Independent of the strain rate, this stress maximum occurred at approximately half the strain at the stress maximum under startup shear. The time dependence of the segment orientation revealed that the molecular origin of the stress maximum can be attributed to the maximum in the corresponding orientation anisotropy, in direct analogy to the behavior under shear.</p>
収録刊行物
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- 日本レオロジー学会誌
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日本レオロジー学会誌 48 (1), 43-48, 2020-02-14
一般社団法人 日本レオロジー学会
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詳細情報 詳細情報について
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- CRID
- 1390846609811978112
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- NII論文ID
- 130007808525
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- NII書誌ID
- AN00198812
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- ISSN
- 21864586
- 03871533
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- NDL書誌ID
- 030269907
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- 本文言語コード
- en
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- データソース種別
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