Constant force extensional rheometry of polymer solutions

被引:31
|
作者
Szabo, Peter [1 ]
McKinley, Gareth H. [2 ]
Clasen, Christian [3 ]
机构
[1] Tech Univ Denmark, Dept Chem & Biochem Engn, DK-2800 Kongens Lyngby, Denmark
[2] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[3] Katholieke Univ Leuven, Dept Chem Engn, B-3001 Heverlee, Belgium
关键词
Extensional rheometry; Filament stretching; Polymer solutions; Extensibility; FILAMENT STRETCHING RHEOMETER; FINITE-ELEMENT-METHOD; CAPILLARY BREAKUP; RHEOLOGICAL PROPERTIES; ELONGATIONAL BEHAVIOR; VISCOELASTIC JETS; RELAXATION-TIMES; DILUTE; VISCOSITY; FLUIDS;
D O I
10.1016/j.jnnfm.2011.11.003
中图分类号
O3 [力学];
学科分类号
08 ; 0801 ;
摘要
We revisit the rapid stretching of a liquid filament under the action of a constant imposed tensile force, a problem which was first considered by Matta and Tytus [J. Non-Newton. Fluid Mech. 35 (1990) 215-229]. A liquid bridge formed from a viscous Newtonian fluid or from a dilute polymer solution is first established between two cylindrical disks. The upper disk is held fixed and may be connected to a force transducer while the lower cylinder falls due to gravity. By varying the mass of the falling cylinder and measuring its resulting acceleration, the viscoelastic nature of the elongating fluid filament can be probed. In particular, we show that with this constant force pull (CFP) technique it is possible to readily impose very large material strains and strain rates so that the maximum extensibility of the polymer molecules may be quantified. This unique characteristic of the experiment is analyzed numerically using the FENE-P model and two alternative kinematic descriptions; employing either an axially-uniform filament approximation or a quasi two-dimensional Lagrangian description of the elongating thread. In addition, a second order pertubation theory for the trajectory of the falling mass is developed for simple viscous filaments. Based on these theoretical considerations we develop an expression that enables estimation of the finite extensibility parameter characterizing the polymer solution in terms of quantities that can be extracted directly from simple measurement of the time-dependent filament diameter. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:26 / 41
页数:16
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