Diffusion coefficients of the monomer and oligomers in hydroxyethyl methacrylate

被引:25
作者
Strauch, J
McDonald, J
Chapman, BE
Kuchel, PW
Hawkett, BS
Roberts, GE
Tonge, MP
Gilbert, RG [1 ]
机构
[1] Univ Sydney, Sch Chem F11, Key Ctr Polymer Colloids, Sydney, NSW 2006, Australia
[2] Univ Sydney, Sch Mol & Microbial Biosci, Sydney, NSW 2006, Australia
[3] Univ New S Wales, Sch Chem Engn & Ind Chem, Ctr Adv Macromol Design, Sydney, NSW 2052, Australia
[4] Univ Stellenbosch, Dept Chem, Afdeling Polimeerwetenskap, ZA-7602 Matieland, South Africa
关键词
diffusion; kinetics (polym.); macromonomers; oligomers; radical polymerization;
D O I
10.1002/pola.10789
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 diffusion coefficients are reported of rubbery ternary systems consisting of the polymer, its monomer analogue (i.e., the saturated equivalent of the monomer), and trace quantities of oligomers (dimer, trimer, tetramer and hexamer) for 2-hydroxyethyl methacrylate (HEMA). These have been obtained with pulsed-field-gradient NMR spectroscopy with a polymer weight fraction (f(p)) of 0 less than or equal to fp less than or equal to 0.4. The oligomers are macromonomers synthesized with a cobalt catalytic chain-transfer agent. The diffusion coefficients are about an order of magnitude smaller than those for monomers such as methyl methacrylate; this effect is ascribed to hydrogen bonding in HEMA. The diffusion coefficient D-i of an i-meric oligomer has been fitted with moderate accuracy by an empirical universal scaling relation, D-i(f(p))/D-1(f(p)) approximate to i(-(0.66+2fp)), previously found to provide an adequate fit to corresponding data for styrene and for methyl and butyl methacrylates. The approximate empirical scaling relation seems to hold for a remarkably wide range of types of monomer/polymer systems. These results are of use in modeling rates and molecular weight distributions in free-radical polymerization, particularly for termination (which is chain-length-dependent and is controlled by the diffusion coefficient of chains of the low degrees of polymerization studied here). (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:2491 / 2501
页数:11
相关论文
共 51 条
[1]   COPOLYMERIZATIONS INVOLVING N-VINYL-2-PYRROLIDONE [J].
ALISSA, MA ;
DAVIS, TP ;
HUGLIN, MB ;
YIP, DCF .
POLYMER, 1985, 26 (12) :1869-1874
[2]   Kinetics and mechanism of controlled free-radical polymerization of styrene and n-butyl acrylate in the presence of an acyclic β-phosphonylated nitroxide [J].
Benoit, D ;
Grimaldi, S ;
Robin, S ;
Finet, JP ;
Tordo, P ;
Gnanou, Y .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (25) :5929-5939
[3]   Critically evaluated termination rate coefficients for free-radical polymerization, 1 - The current situation [J].
Buback, M ;
Egorov, M ;
Gilbert, RG ;
Kaminsky, V ;
Olaj, OF ;
Russell, GT ;
Vana, P ;
Zifferer, G .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 2002, 203 (18) :2570-2582
[4]  
Buback M, 2001, MACROMOL THEOR SIMUL, V10, P209, DOI 10.1002/1521-3919(20010401)10:4<209::AID-MATS209>3.3.CO
[5]  
2-Q
[6]   COBALOXIME AS A CATALYTIC CHAIN TRANSFER AGENT [J].
BURCZYK, AF ;
ODRISCOLL, KF ;
REMPEL, GL .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 1984, 22 (11) :3255-3262
[7]  
Callaghan P.T., 1991, Principles of nuclear magnetic resonance microscopy, V1st
[8]   PULSED FIELD GRADIENT NUCLEAR MAGNETIC-RESONANCE AS A PROBE OF LIQUID-STATE MOLECULAR-ORGANIZATION [J].
CALLAGHAN, PT .
AUSTRALIAN JOURNAL OF PHYSICS, 1984, 37 (04) :359-387
[9]   Experimental determination of the rate constant of deactivation of poly(styrene) and poly(butyl acrylate) radicals in atom transfer radical polymerization [J].
Chambard, G ;
Klumperman, B ;
German, AL .
MACROMOLECULES, 2002, 35 (09) :3420-3425
[10]   MOLECULAR-WEIGHT DISTRIBUTIONS IN FREE-RADICAL POLYMERIZATIONS .1. MODEL DEVELOPMENT AND IMPLICATIONS FOR DATA INTERPRETATION [J].
CLAY, PA ;
GILBERT, RG .
MACROMOLECULES, 1995, 28 (02) :552-569