Sub-micrometer thermoplastic vulcanizates obtained by reaction-induced phase separation of miscible mixtures of poly(ethylene) and alkyl methacrylates

被引:24
作者
I'Abee, Roy [1 ,2 ]
Goossens, Han [1 ,2 ]
van Duin, Martin [1 ,3 ]
Spoelstra, Anne [1 ]
机构
[1] Eindhoven Univ Technol, Dept Chem Engn & Chem, Lab Polymer Technol, NL-5600 MB Eindhoven, Netherlands
[2] Dutch Polymer Inst, NL-5600 AX Eindhoven, Netherlands
[3] DSM Res & Patents, NL-6160 MD Geleen, Netherlands
关键词
Grafting and cross-linking reactions; Mechanical properties; Miscibility; Reaction-induced phase separation; Thermoplastic vulcanizates; INTERPENETRATING POLYMER NETWORKS; POLYOXYETHYLENE/POLYSTYRENE BLENDS; ELASTOMER BLENDS; IN-SITU; POLYETHYLENE; MORPHOLOGY; DEGRADATION; BEHAVIOR; RUBBER; POLYPROPYLENE;
D O I
10.1016/j.eurpolymj.2008.11.002
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Sub-micrometer (mu m) thermoplastic vulcanizates (TPVs) with cross-linked rubber particles with sizes ranging from 70 to 400 nm were prepared by reaction-induced phase separation (RIPS) of initially miscible blends of poly(ethylene) (PE), lauryl methacrylate (LMA) and divinylbenzene (DVB). Cross-linking under static conditions led to (partial) connectivity of the rubber particles via chemical bridging of grafted PE chains. Dynamic preparation conditions caused the connected structure to break-up, which led to a significant enhancement of the mechanical properties and the melt processability. The addition of 25-80 wt% extender oil resulted in a reduced complex viscosity and yield stress in the melt, without deteriorating the mechanical properties. The relatively good elastic recovery and excellent ultimate properties of these high hardness TPVs may be explained by the sub-pm rubber dispersions. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:503 / 514
页数:12
相关论文
共 46 条
[1]  
Araghi H. H., 2001, P INT RUBB C BIRM UK
[2]   Shear viscosity of rubber modified thermoplastics: Dynamically vulcanized thermoplastic elastomers and ABS resins at very low stress [J].
Araki, T ;
White, JL .
POLYMER ENGINEERING AND SCIENCE, 1998, 38 (04) :590-595
[3]  
*ASTM, 1986, D412 ASTM
[4]  
*ASTM, 1989, D395 ASTM
[5]   Polymerization-induced phase separation .1. Conversion-phase diagrams [J].
Boots, HMJ ;
Kloosterboer, JG ;
Serbutoviez, C ;
Touwslager, FJ .
MACROMOLECULES, 1996, 29 (24) :7683-7689
[6]   STRUCTURE AND PROPERTIES OF AN INTERPENETRATING POLYMER NETWORK-LIKE SYSTEM CONSISTING OF POLYSTYRENE POLYETHYLENE .1. SYNTHESIS, ELASTOMERIC AND THERMOANALYTICAL CHARACTERIZATION [J].
BORSIG, E ;
FIEDLEROVA, A ;
HAUSLER, KG ;
SAMBATRA, RM ;
MICHLER, GH .
POLYMER, 1993, 34 (22) :4787-4792
[7]   MODIFICATION OF POLYETHYLENE WITH METHACRYLIC-ACID .1. GRAFTING OF METHACRYLIC-ACID ONTO POLYETHYLENE [J].
BRYJAK, M ;
TROCHIMCZUK, W .
ANGEWANDTE MAKROMOLEKULARE CHEMIE, 1983, 116 (SEP) :221-224
[8]   MODIFICATION OF POLYETHYLENE WITH METHACRYLIC-ACID .2. MOLECULAR-STRUCTURE OF THE GRAFTED COPOLYMER [J].
BRYJAK, M ;
TROCHIMCZUK, W .
ANGEWANDTE MAKROMOLEKULARE CHEMIE, 1983, 118 (DEC) :191-195
[9]   RUBBER-THERMOPLASTIC COMPOSITIONS .1. EPDM-POLYPROPYLENE THERMOPLASTIC VULCANIZATES [J].
CORAN, AY ;
PATEL, R .
RUBBER CHEMISTRY AND TECHNOLOGY, 1980, 53 (01) :141-150
[10]  
CORAN AY, 1978, SCI TECHNOL RUBBER