Surface tension driven jet break up of strain-hardening polymer solutions

被引:174
作者
Christanti, Y [1 ]
Walker, LM [1 ]
机构
[1] Carnegie Mellon Univ, Ctr Complex Fluids Engn, Dept Chem Engn, Pittsburgh, PA 15213 USA
关键词
jet break up; polymer solutions; viscoelasticity; opposed-nozzle rheometer;
D O I
10.1016/S0377-0257(01)00135-5
中图分类号
O3 [力学];
学科分类号
08 ; 0801 ;
摘要
Experimental studies attempting to ascertain the influence of viscoelasticity on the atomization of polymer solution are often hindered by the inability to decouple the effect of shear thinning from the effect of extensional hardening. Here, the influence of viscoelasticity on the jet break up of a series of non-shear-thinning viscoelastic fluids is quantified. Previous characterization using an opposed-nozzle rheometer identified the critical extensional rates for strain hardening of these model fluids. The strain hardening fluids exhibit a beads-on-string structure with reduction or elimination of satellite drops. Capillary instabilities grow on the filaments connecting the spheres and eventually break the filaments up into a string of very small drops about one order of magnitude smaller than the satellite drops formed by a Newtonian fluid with the same shear viscosity, surface tension, and density. These results confirm that strain hardening is the key rheological property in jet break up and that the critical extensional rate of a fluid is pertinent in determining the final characteristics of break up. Results suggest that the opposed-nozzle rheometer does probe extensional behavior in the range of extensional rates that are relevant to jet break up, providing a tool to roughly predict jet break up. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:9 / 26
页数:18
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