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Dynamic and slip phenomena of surface polymer using evanescent wave laser optical polarimetry and plane-Couette shear rheometry.

机译:使用e逝波激光旋光仪和平面-库埃特剪切流变仪测定表面聚合物的动态和滑移现象。

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The dynamic of surface polymer as well as the slip, stick-slip phenomena at the polymer-solid interface were investigated using the Evanescent Wave Laser Optical Polarimetry (EWLP) and plane-Couette shear flow apparatus. Time-dependent step strain EWLP relaxation experiments using 1,4-polybutadiene melts indicate that a single exponential function completely describes orientation relaxation dynamics of fluid near the substrate. The characteristic decay time tsurface determined from these experiments was found to be a much stronger function of bulk polymer molecular weight tsurface∼M4.2±0.03 W than the corresponding terminal properties of 1,4-polybutadiene melts in bulk, h0M&d1;3 .4±0.02W and td0M&d1; 3.4±0.04W . Comparison of the MW-dependence of tsurface with theoretical expectations for several alternative molecular mechanisms indicate that a constraint release tube renewal mechanism best explains the experimental observations. The sliding plate plane-Couette shear flow apparatus can be used to investigate the stick-slip phenomena of the polymer at the surface or the instabilities at the fluid and solid surface for complex fluid such as polymer. The stick-slip flow regime phenomena in the polybutadienes-aluminum interface is originated from the flow induced disentanglement of the physisorbed chains and the bulk polymer network. The onset to the stick-slip regime of the polymer has some dependence to the bulk state of the polymer. The critical stress is in the order of the plateau modulus and can be predicted from the Mhetar and Archer scaling theory which is Ge/(Ne) 1/2. A small change in the bidisperse polymer can greatly reduce the stick-slip phenomena and the existing of smaller chain polymer promote the slippage at the solid surface. The stick-slip flow regime phenomena of the polymer blend of PBD 335K and PBD 176K is originated from the flow induced disentanglement of the physisorbed chains and the bulk polymer network. The result from the lower grafting density substrate also reassured us about the results from previous studies that the stick-slip behavior was originated from the flow-induced disentanglement between bulk polymer and anchored chains at the surface.
机译:使用van逝波激光旋光仪(EWLP)和平面-库埃特剪切流变仪研究了表面聚合物的动力学以及聚合物-固体界面处的滑移,粘滑现象。使用1,4-聚丁二烯熔体的随时间变化的阶跃应变EWLP弛豫实验表明,单个指数函数完全描述了基底附近流体的取向弛豫动力学。从这些实验中确定的特征衰变时间 t 被发现比本体聚合物分子具有更强的功能重量<数学> t 表面〜M 4.2±0.03 W ,而不是1,4-聚丁二烯的相应末端性质, h 0 < ac> M &d1; 3 .4±0.02 W t d0 M &d1; < / a> 3.4±0.04 W 。对 t 曲面 的M W 依赖性的比较以及对几种方法的理论期望替代的分子机制表明,约束释放管的更新机制最能解释实验结果。滑板式平面Couette剪切流动仪可用于研究聚合物在表面的粘滑现象或复杂流体(例如聚合物)在流体和固体表面的不稳定性。聚丁二烯-铝界面中的粘滑流动状态现象是由物理吸附链和本体聚合物网络的流动诱导的解缠引起的。聚合物的粘滑状态的开始对聚合物的本体状态有一定的依赖性。临界应力约为平台模量,可以根据Mhetar和Archer缩放理论预测,即G e /(N e 1 / 2 。双分散聚合物的微小变化可大大减少粘滑现象,较小链状聚合物的存在会促进固体表面的滑移。 PBD 335K和PBD 176K聚合物共混物的粘滑流动状态现象是由流动引起的物理吸附链和本体聚合物网络的解缠引起的。较低接枝密度的底物的结果也使我们对以前的研究结果感到放心,即粘滑行为是由流动引起的松散聚合物与表面锚链之间的缠结引起的。

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