Synthesis and reactive blending of amine and anhydride end-functional polyolefins

被引:21
作者
Jones, TD
Macosko, CW
Moon, BJ
Hoye, TR
机构
[1] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
polymer blends; drop morphology; polyethylene;
D O I
10.1016/j.polymer.2004.04.015
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polyolefins having low polydispersity and containing terminal functional groups are difficult to synthesize, due to limitations in catalysis technology. We have developed methods for preparing model polyolefins with terminal amine or anhydride functionality and of controlled molecular weight and narrow polydispersity. Both 1,4- or 1,2-polybutadienes are prepared by living anionic polymerization, with introduction of a functional group precursor during chain termination. The functional groups are protected as tert-butyl carbamate and tertbutyl ester for the amine and anhydride, respectively. The polymers are hydrogenated heterogeneously, with subsequent deprotection yielding saturated polymers with functionalities of up to 90%. These materials, due to their low polydispersity, comprise a useful model system for measuring melt reaction kinetics by gel permeation chromatography. Melt blending of amine- and anhydride-functional PEE90 (polyethylethylene) with complementary functional polystyrenes quickly yields extensive amounts of block copolymer with complex, submicron scale morphologies. Similar fine morphologies are observed for blends of amine- and anhydride-functional PE (polyethylene) with functional polystyrene. These functional PE and PEE90 polymers can also be used as reactive compatibilizers for polyethylene and polypropylene blends, respectively. The concentration of compatibilizer required to obtain sub-micron particles, however, is as high as 20% by weight. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4189 / 4201
页数:13
相关论文
共 66 条
[1]   SYNTHESIS AND CHARACTERIZATION OF A MODEL SATURATED-HYDROCARBON DIBLOCK COPOLYMER [J].
BATES, FS ;
ROSEDALE, JH ;
BAIR, HE ;
RUSSELL, TP .
MACROMOLECULES, 1989, 22 (06) :2557-2564
[2]   Anionic synthesis of polymers functionalized with a terminal anhydride group [J].
Cernohous, JJ ;
Macosko, CW ;
Hoye, TR .
MACROMOLECULES, 1997, 30 (18) :5213-5219
[3]   Amine-terminal polystyrenes: A new strategy for synthesis and new methods for determination of functionality [J].
Cernohous, JJ ;
Macosko, CW ;
Hoye, TR .
MACROMOLECULES, 1998, 31 (12) :3759-3763
[4]  
Chaffin KA, 2000, J POLYM SCI POL PHYS, V38, P108, DOI 10.1002/(SICI)1099-0488(20000101)38:1<108::AID-POLB14>3.0.CO
[5]  
2-9
[6]  
CHAFFIN KA, 1999, DEP CHEM ENG MAT SCI
[7]   Reactive compatibilization of polypropylene polyethylene terephthalate blends [J].
Champagne, MF ;
Huneault, MA ;
Roux, C ;
Peyrel, W .
POLYMER ENGINEERING AND SCIENCE, 1999, 39 (06) :976-984
[8]   Reactive blending of polysulfone with polyamide: a difference in interfacial behavior between in situ formed block and graft copolymers [J].
Charoensirisomboon, P ;
Chiba, T ;
Solomko, SI ;
Inoue, T ;
Weber, M .
POLYMER, 1999, 40 (24) :6803-6810
[9]   A novel synthesis of PP-b-PMMA copolymers via metallocene catalysis and borane chemistry [J].
Chung, TC ;
Lu, HL ;
Janvikul, W .
POLYMER, 1997, 38 (06) :1495-1502
[10]   GRAFT COPOLYMER COMPATIBILIZERS FOR BLENDS OF ISOTACTIC POLYPROPYLENE AND ETHENE PROPENE COPOLYMERS .2. FUNCTIONAL POLYMERS APPROACH [J].
DATTA, S ;
LOHSE, DJ .
MACROMOLECULES, 1993, 26 (08) :2064-2076