VISCOSITIES OF MODERATELY CONCENTRATED SOLUTIONS OF POLYETHYLENE IN ETHANE PROPANE AND ETHYLENE

被引:13
作者
EHRLICH, P
WOODBREY, JC
机构
[1] Monsanto Company, Hydrocarbons and Polymers Division, Research Department, Springfield, Massachusetts
[2] Department of Chemical Engineering, State University of New York at Buffalo, Buffalo, New York
[3] Monsanto Company, New Enterprises Division, Research Center, St Louis, Missouri
关键词
D O I
10.1002/app.1969.070130113
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The viscosities of moderately concentrated solutions of low‐density polyethylenes in ethane, propane, and ethylene have been measured at low shear rate in the temperature range of 150–250°C and in the pressure range of about 15000–30000 psi. Within the precision of the measurements, the relative viscosity is independent of pressure over the range investigated but increases as the solvent is changed from propane through ethane to ethylene. The activation energy for the relative viscosity in ethane varies from about 0.5 to 2.5 kcal/mole as the concentration changes from 5 to 15 g/dl. Effects of polymer concentration and molecular weight on solution viscosity in ethane at 150°C have been determined, and all of the data can be represented by a single straight‐line plot of the logarithm of relative viscosity versus the intrinsic viscosity (in p‐xylene at 105°C) times concentration. This simple relation is valid over wide ranges of polymer concentration and molecular weight and over more than two orders of magnitude of relative viscosity. The solution viscosities of the polyethylenes in the three supercritical fluid solvents used appear surprisingly low at first sight. This behavior is partly a result of the low solvent viscosities but also might mean that the polymer has an abnormally low segmental friction factor compared to that in solutions under more familiar conditions. Copyright © 1969 John Wiley & Sons, Inc.
引用
收藏
页码:117 / &
相关论文
共 19 条
[1]   INTERMOLECULAR FORCES AND CHAIN FLEXIBILITIES IN POLYMERS .2. INTERNAL PRESSURES OF POLYMERS [J].
ALLEN, G ;
GEE, G ;
MANGARAJ, D ;
SIMS, D ;
WILSON, GJ .
POLYMER, 1960, 1 (04) :467-476
[2]  
BUECHE F, 1962, PHYSICAL PROPERTIES, pCH4
[3]  
CARR NL, 1955, CHEM ENG PROGR S SER, V51, P91
[4]   PHASE EQUILIBRIA OF POLYMER-SOLVENT SYSTEMS AT HIGH PRESSURES NEAR THEIR CRITICAL LOCI .2. POLYETHYLENE-ETHYLENE [J].
EHRLICH, P .
JOURNAL OF POLYMER SCIENCE PART A-GENERAL PAPERS, 1965, 3 (1PA) :131-&
[5]   PHASE EQUILIBRIA OF POLYMER-SOLVENT SYSTEMS AT HIGH PRESSURES NEAR THEIR CRITICAL LOCI - POLYETHYLENE WITH N-ALKANES [J].
EHRLICH, P ;
KURPEN, JJ .
JOURNAL OF POLYMER SCIENCE PART A-GENERAL PAPERS, 1963, 1 (10) :3217-&
[6]   A KINETIC STUDY OF THE OXYGEN-INITIATED POLYMERIZATION OF ETHYLENE [J].
EHRLICH, P ;
PITTILO, RN .
JOURNAL OF POLYMER SCIENCE, 1960, 43 (142) :389-412
[7]  
GILCHRIST A, 1964, MAR FAR SOC INF DIS
[8]   The rolling ball viscometer [J].
Hubbard, RM ;
Brown, GG .
INDUSTRIAL AND ENGINEERING CHEMISTRY-ANALYTICAL EDITION, 1943, 15 :212-218
[9]  
HUGGINS ML, 1955, CELLULOSE ITS DERI 3, P1189
[10]  
HUGGINS ML, 1955, CELLULOSE ITS DERI 3, P1203