Melt rheology of polypropylene containing small amounts of high-molecular-weight chain. 2. Uniaxial and biaxial extensional flow

被引:82
作者
Sugimoto, M [1 ]
Masubuchi, Y [1 ]
Takimoto, J [1 ]
Koyama, K [1 ]
机构
[1] Yamagata Univ, Dept Mat Sci & Engn, Yonezawa, Yamagata 9928510, Japan
关键词
D O I
10.1021/ma0015525
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Uniaxial extensional flow behavior was measured for the high-melt-strength polypropylene using a Meissner-type rheometer under transient extensional flow with constant tensile strain rate. The equibiaxial extensional flow behavior of the high-melt-strength polypropylene was measured via the lubricated squeezing flow method under constant strain rate. The high-melt-strength polypropylene consists of polypropylene (PP) as a main component and high-molecular-weight polyethylene (PE) component as a long relaxation time component (see part 1). This system is generally believed to be an immiscible system, at least under the quiescent state. Nevertheless, in part 1, we have found that the high-melt-strength PP with very high-molecular-weight PE shows distinctly different shear flow behaviors from conventional PP, e.g., high elasticity and two-step viscosity at low shear rates and strong and weak strain-dependent nonlinear damping functions characterizing fast and slow relaxation processes. In this study, the transient uniaxial viscosity of the high-melt-strength PP melts first increased gradually with time, following the linear viscoelastic rule in which the uniaxial extensional viscosity is 3 times the shear viscosity development. Beyond a certain critical strain, the uniaxial extensional viscosity showed rapid increase, which was referred to as strain hardening. Furthermore, the transient biaxial extensional viscosity showed also the strain hardening behavior over a critical strain. These prominent behaviors are unexpected for conventional PP. The nonlinear upturn behavior was discussed from a high-molecular weight chain stretching point of view via molecular constitutive equations given by Osaki et al. for bimodal polymer blends.
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页码:6056 / 6063
页数:8
相关论文
共 47 条
[1]   ON THE LAMELLAR MORPHOLOGY OF ISOTACTIC POLYPROPYLENE SPHERULITES [J].
BASSETT, DC ;
OLLEY, RH .
POLYMER, 1984, 25 (07) :935-943
[2]  
CHATRAEI S, 1981, J RHEOL, V25, P433, DOI 10.1122/1.549648
[3]   COMMENTS ON INTRINSIC VISCOSITY-WEIGHT-AVERAGE MOLECULAR WEIGHT RELATIONSHIPS FOR POLYETHYLENE [J].
CHIANG, R .
JOURNAL OF POLYMER SCIENCE, 1959, 36 (130) :91-103
[4]   MULTIAXIAL ELONGATIONS OF POLYISOBUTYLENE AND THE PREDICTIONS OF SEVERAL NETWORK THEORIES [J].
DEMARMELS, A ;
MEISSNER, J .
COLLOID AND POLYMER SCIENCE, 1986, 264 (10) :829-846
[5]  
Doi M., 1986, The Theory of Polymer Dynamics
[6]   BIAXIAL EXTENSIONAL FLOW BEHAVIOR OF MONODISPERSE POLYSTYRENE MELTS [J].
EBRAHIMI, NG ;
TAKAHASHI, M ;
ARAKI, O ;
MASUDA, T .
ACTA POLYMERICA, 1995, 46 (03) :267-271
[7]   Determination of plateau moduli and entanglement molecular weights of isotactic, syndiotactic, and atactic polypropylenes synthesized with metallocene catalysts [J].
Eckstein, A ;
Suhm, J ;
Friedrich, C ;
Maier, RD ;
Sassmannshausen, J ;
Bochmann, M ;
Mulhaupt, R .
MACROMOLECULES, 1998, 31 (04) :1335-1340
[8]  
HIGMANN R, 1994, J RHEOL, V38, P573
[9]   ELONGATIONAL VISCOSITY AT A CONSTANT ELONGATIONAL STRAIN RATE OF POLYPROPYLENE MELT [J].
ISHIZUKA, O ;
KOYAMA, K .
POLYMER, 1980, 21 (02) :164-170
[10]   COMPARISON OF THE RHEOLOGY OF POLYMER MELTS IN SHEAR, AND BIAXIAL AND UNIAXIAL EXTENSIONS [J].
KHAN, SA ;
PRUDHOMME, RK ;
LARSON, RG .
RHEOLOGICA ACTA, 1987, 26 (02) :144-151