Stretch-orientation-induced reduction of friction in well-entangled bidisperse blends: a dual slip-link simulation study
Stretch-orientation-induced reduction of friction in well-entangled bidisperse blends: a dual slip-link simulation study
复制标题
良好缠结的双分散共混物中拉伸取向引起的摩擦减少:双滑移连接模拟研究
DOI:
10.1007/s00397-022-01378-5
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发表时间:
2022
期刊:
影响因子:
2.3
通讯作者:
Taniguchi Takashi
中科院分区:
文献类型:
--
作者:
Miyamoto Souta;Sato Takeshi;Taniguchi Takashi
We investigated the rheological properties of bidisperse entangled-polymer blends under high-deformation-rate flows by slip-link simulations with a friction reduction mechanism. The friction reduction mechanism induced by the stretch and orientation (SORF) is important to predict the viscoelasticity under uniaxial elongational flows. To test the applicability of this mechanism for bidisperse systems, we incorporated an expression of friction reduction (Yaoita et al.Macromolecules45:2773–2782 ) into the Doi-Takimoto slip-link model (DT model) (Doi and TakimotoPhilos Trans R Soc Lond A361:641–652 ). For six experimental bidisperse systems, i.e., four polystyrene blends and two polyisoprene blends, the extended DT model where the order parameter of the friction reduction mechanism is evaluated through the component averages succeeds in reproducing the data under uniaxial elongation and shear. This success is due to the suppression of the stretch of the longer chains using the statistical average over each component. Through this study, the SORF expression improves the rheological prediction for bidisperse entangled polymer melts under uniaxial elongational flows with strain rates comparable to or larger than the inverse of the Rouse relaxation time of the longer chains. Additionally, the predictions with the SORF using the component average for the stretches reproduce the steady viscosities because under elongational flows, the states of the components with different molecular weights clearly differ from each other depending on their Rouse relaxation time. The finding means that for chain dynamics, the friction coefficient is determined by the state of the surrounding polymer chains and the state of the chain.