材料科学
打滑(空气动力学)
毛细管作用
聚合物
挤出胀大
复合材料
天然橡胶
热力学
挤压
物理
作者
Xiaoping Yang,Hatsuo Ishida,Shi‐Qing Wang
摘要
We conduct a comprehensive experimental study of melt/wall interfacial slip behavior of various polymer melts in capillary flow. Polymers under study include two polystyrenes of different molecular weights (MW=280 000 and MW=2×106, respectively), two low-density polyethylenes (LDPE), poly(ethylene vinyl acetate) (EVA), and polypropylene (PP). The experimental results reveal an important finding that has greatly extended our previous knowledge of the roles of melt/wall interfacial interactions and molecular entanglements in dictating capillary melt flow behavior. None of the six polymers exhibits an interfacial stick–slip transition or shows any sign of wall slip in bare aluminum dies. Yet, all are found to display a sizable wall slip when the strength of polymer/surface adsorption is reduced by lowering the die wall surface energy with a fluoropolymer coating. The degree of wall slip as characterized by the Navier–de Gennes extrapolation length is demonstrated to be explicitly proportional to the melt viscosity, such that the magnitude of wall slip in the coated die decreases with increasing shear thinning. Diminishing of a measurable wall slip at high stresses explains the well-known absence of spurt, flow oscillation, and sharkskin phenomena in capillary flow of commonly encountered polymers such as PS, LDPE, PP.
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