Wall Slip Behaviors of Crystallized Polypropylene under Oscillatory Shear

IF 5.1 1区 化学 Q1 POLYMER SCIENCE
Xinyang Zhao, Yadong Lu, Fengyi Hou, Li Peng, Xianbo Huang, Wei Yu
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Abstract

Compared to the wall slip of polymer melts, less attention has been paid to the wall slip of viscoelastic solids, such as crystallized polymer. The existence of the wall slip of crystallized polymers not only prevents the precise measurement of their viscoelastic properties but also leads to flow instabilities during polymer processing like injection molding. In this work, a continuous cyclic strain sweep test is designed to resolve the wall slip behaviors of crystallized polypropylene under large-amplitude oscillatory shear at different temperatures. A stick–slip transition is identified, and its critical conditions are discussed in relation to the crystallinity. A rheo-electric measurement is performed to reveal the interfacial process during the development of wall slip. At relatively low temperatures (below 145 °C), wall slip is found to take place in advance of bulk structural changes. In this case, a quantitative method is proposed to extract the transient slip rate from the apparent stress. A weak slip regime, a transition regime, and a strong slip regime where the slip rate exhibits different strain dependence are identified. Finally, the effects of surface topography and surface free energy on the wall slip behaviors are discussed.

Abstract Image

振荡剪切作用下结晶聚丙烯的壁滑移行为
与聚合物熔体的壁面滑移相比,粘弹性固体(如结晶聚合物)的壁面滑移受到的关注较少。结晶聚合物的壁滑移不仅阻碍了其粘弹性性能的精确测量,而且在注塑等聚合物加工过程中导致流动不稳定。本文设计了连续循环应变扫描试验,研究了不同温度下大振幅振荡剪切作用下结晶聚丙烯的壁滑移行为。确定了粘滑转变,并讨论了其与结晶度的关系的临界条件。通过流变电测量揭示了壁滑发展过程中的界面过程。在相对较低的温度下(低于145°C),墙体滑移在整体结构变化之前发生。在这种情况下,提出了一种从视应力中提取瞬态滑移率的定量方法。确定了弱滑移区、过渡区和强滑移区,其中滑移率表现出不同的应变依赖性。最后讨论了表面形貌和表面自由能对壁面滑移行为的影响。
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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