Styrene/acrylic acid random copolymers synthesized by nitroxide-mediated polymerization: Effect of free nitroxide on kinetics and copolymer composition

被引:51
作者
Lessard, Benoit [1 ]
Schmidt, Scott C.
Maric, Milan [1 ]
机构
[1] McGill Univ, CSACS, MIAM, Dept Chem Engn, Montreal, PQ H3A 2B2, Canada
关键词
D O I
10.1021/ma0718604
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Styrene/acrylic acid (S/AA) mixtures were copolymerized in concentrated 50 wt % 1,4-dioxane solutions at 120 degrees C at two ratios of additional free nitroxide mediator, N,N-tert-butyl-N-[1'-diethylphosphono2,2'-dimethylpropyl] nitroxide (SG1), relative to 2-[N-tert-butyl-2,2-(dimethylpropyl)aminooxy]propionic acid (BlocBuilder, Arkema) alkoxyamine unimolecular initiator (4.5 and 9 mol % [SG1]/[BlocBuilder]). Without SG1 at initial acrylic acid monomer feed concentrations f(AA,0) > 40 mol %, the apparent rate constants increased sharply, noticeable exotherms were observed, and polydispersities increased from 1.20 at f(AA,0) = 0 MOl % to 1.48 at f(AA,0) = 80 mol %. With 4.5 mol % [SG1]/[BlocBuilder], polymerization rates were slower and not as strongly affected by f(AA,0) although exotherms were still noticeable at high f(AA,0). Polydispersities remained similar to 1.3 and only increased to > 1.4 at high conversions for f(AA,0) = 80 mol %. Exotherms were rendered nearly negligible when 9 mol % [SG1]/[BlocBuilder] was used, leading to copolymers with much narrower molecular weight distributions and k(p)K values for comonomer mixtures bracketed between those of styrene and acrylic acid homopolymerizations at 120 degrees C (k(p) = propagation rate constant, K = equilibrium constant). Copolymer reactivity ratios estimated for samples produced using 9 mol % [SG1]/[BlocBuilder] by nonlinear least-squares minintization were r(AA) = 0.25 +/- 0.11 and r(s) = 0.93 +/- 0.37, in agreement with previous literature.
引用
收藏
页码:3446 / 3454
页数:9
相关论文
共 54 条
[1]   The "living" free radical synthesis of poly(4-hydroxystyrene): Physical properties and dissolution behavior [J].
Barclay, GG ;
Hawker, CJ ;
Ito, H ;
Orellana, A ;
Malenfant, PRL ;
Sinta, RF .
MACROMOLECULES, 1998, 31 (04) :1024-1031
[2]  
Baumann M, 2000, MACROMOL CHEM PHYS, V201, P2751, DOI 10.1002/1521-3935(20001201)201:18<2751::AID-MACP2751>3.0.CO
[3]  
2-Z
[4]   Synthesis of oxazoline-terminated polystyrene via controlled-radical polymerization [J].
Baumert, M ;
Zimmermann, J ;
Scherble, J ;
Mülhaupt, R ;
Kressler, J .
MACROMOLECULES, 1999, 32 (08) :2403-2409
[5]   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
[6]   Determination of free-radical propagation rate coefficients of butyl, 2-ethylhexyl, and dodecyl acrylates by pulsed-laser polymerization [J].
Beuermann, S ;
Paquet, DA ;
McMinn, JH ;
Hutchinson, RA .
MACROMOLECULES, 1996, 29 (12) :4206-4215
[7]   Controlled radical polymerization of 4-vinylpyridine [J].
Bohrisch, J ;
Wendler, U ;
Jaeger, W .
MACROMOLECULAR RAPID COMMUNICATIONS, 1997, 18 (11) :975-982
[8]   Cavitated block copolymer micellar thin films: Lateral arrays of open nanoreactors [J].
Boontongkong, Y ;
Cohen, RE .
MACROMOLECULES, 2002, 35 (09) :3647-3652
[9]   CRITICALLY EVALUATED RATE COEFFICIENTS FOR FREE-RADICAL POLYMERIZATION .1. PROPAGATION RATE COEFFICIENT FOR STYRENE [J].
BUBACK, M ;
GILBERT, RG ;
HUTCHINSON, RA ;
KLUMPERMAN, B ;
KUCHTA, FD ;
MANDERS, BG ;
ODRISCOLL, KF ;
RUSSELL, GT ;
SCHWEER, J .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 1995, 196 (10) :3267-3280
[10]   COPOLYMERIZATION .7. RELATIVE RATES OF ADDITION OF VARIOUS MONOMERS IN COPOLYMERIZATION [J].
CHAPIN, EC ;
HAM, GE ;
MILLS, CL .
JOURNAL OF POLYMER SCIENCE, 1949, 4 (05) :597-604