Effect of molecular weight on secondary Newtonian plateau at high shear rates for linear isotactic melt blown polypropylenes

被引:29
作者
Drabek, Jiri [1 ]
Zatloukal, Martin [1 ]
Martyn, Mike [2 ]
机构
[1] Tomas Bata Univ Zlin, Fac Technol, Polymer Ctr, Vavreckova 275, Zlin 76001, Czech Republic
[2] Univ Bradford, Sch Engn Design & Technol, IRC Polymer Engn, Bradford BD7 1DP, W Yorkshire, England
关键词
High shear rate rheology; Secondary Newtonian viscosity; Polymer melt; Melt blown; Isotactic polypropylene; Rheological models; PRESSURE CAPILLARY RHEOMETRY; POLYMER MELTS; THERMAL-CONDUCTIVITY; RHEOLOGICAL PROPERTIES; FREE-VOLUME; VISCOSITY; FLOW; DEPENDENCE; BEHAVIOR; FLUIDS;
D O I
10.1016/j.jnnfm.2017.11.009
中图分类号
O3 [力学];
学科分类号
08 ; 0801 ;
摘要
In this work, three melt blown grades of isotactic linear polypropylenes, with weight average molecular weights between 56 250-75 850 g/mol, have been characterized at 230 degrees C over a very wide shear rate range (10-10(7) 1/s) by using conventional rotational and twin bore capillary rheometry equipped with novel orifice die, and by an instrumented capillary nozzle on an injection molding machine. A low shear rate primary Newtonian plateau, a pseudoplastic region and a well developed secondary Newtonian plateau (occurring between 2.10(6) - 7.10(6) 1/s) were identified for all the polypropylene melts. Flow activation energy at low (E-0) and high (E-infinity) shear rates was found to be 56.590 kJ/mol and 25.204 kJ/mol, respectively. Considering the typical value of pressure sensitivity coefficient for polypropylene melt, beta = 20.00 GPa(-1), and measured flow activation energy at the secondary Newtonian plateau, E-infinity = 25.204 kJ/mol, it was found that the effect of viscous dissipation and pressure is mutually cancelled, i.e. that the measured viscosity data can be considered as the true material property within the whole applied shear rate range. For the first time, it has been revealed that the secondary Newtonian viscosity, eta(infinity) depends linearly on the weight average molecular weight, M-W, in log-log scale as eta(infinity) = 1.19.10(-6)M(w)(1.084). The observed slope close to 1 between eta(infinity) and M-w suggests that polymer chains in the melt are disentangled at the secondary Newtonian plateau region. This conclusion is supported by the experimental observation that the high shear rate flow activation energy E-infinity for given PP melts is comparable with the flow activation energy of PP like oligomer (squalane, C30H62; 2,6,10,15,19,23-hexamethyltetracosane). The measured flow data were fitted by six different viscosity models, from which two, namely Modified Carreau and Quemada models, were suggested here for the first time. It has been found that the accuracy of utilized models to describe the measured data is the highest for the newly suggested models and decreases in the following order: Modified Quemada model, Modified Carreau model, Carreau-Yasuda model, Cross model, Generalized Quemada model and Carreau model.
引用
收藏
页码:107 / 118
页数:12
相关论文
共 50 条
[1]  
[Anonymous], 1893, Am. J. Sci, DOI DOI 10.2475/AJS.S3-45.266.87
[2]   Comparison of Molecular Structure and Rheological Properties of Electron-Beam- and Gamma-Irradiated Polypropylene [J].
Auhl, Dietmar ;
Stadler, Florian J. ;
Muenstedt, Helmut .
MACROMOLECULES, 2012, 45 (04) :2057-2065
[3]   Injection of polypropylene reinforced with short glass fibers: Rheological behavior [J].
Benhadou, M. ;
Haddout, A. .
JOURNAL OF REINFORCED PLASTICS AND COMPOSITES, 2007, 26 (13) :1357-1366
[4]   The pressure dependence of the shear and elongational properties of polymer melts [J].
Binding, DM ;
Couch, MA ;
Walters, K .
JOURNAL OF NON-NEWTONIAN FLUID MECHANICS, 1998, 79 (2-3) :137-155
[5]  
Bird R. B., 1987, FLUID MECH, V1
[6]  
Brang J. E., 2008, US Patent, Patent No. [0023888, 20080023888]
[7]   VISCOSITY, SELF-DIFFUSION, AND ALLIED EFFECTS IN SOLID POLYMERS [J].
BUECHE, F .
JOURNAL OF CHEMICAL PHYSICS, 1952, 20 (12) :1959-1964
[8]   Evaluation and comparison of routes to obtain pressure coefficients from high-pressure capillary rheometry data [J].
Cardinaels, Ruth ;
Van Puyvelde, Peter ;
Moldenaers, Paula .
RHEOLOGICA ACTA, 2007, 46 (04) :495-505
[9]   RHEOLOGICAL EQUATIONS FROM MOLECULAR NETWORK THEORIES [J].
CARREAU, PJ .
TRANSACTIONS OF THE SOCIETY OF RHEOLOGY, 1972, 16 (01) :99-&
[10]  
Chapman RA, 2010, WOODHEAD PUBL TEXT, pXVII