Sub-micron pellicular resins as polymer supports

被引:6
作者
Gauthier, M
Frank, PC
机构
[1] Department of Chemistry, Institute for Polymer Research, University of Waterloo, Waterloo
关键词
pellicular resins; styrene-divinylbenzene latex; grafted latex; polymer support design;
D O I
10.1016/1381-5148(96)00050-8
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The synthesis of novel polymer supports was carried out with the aim of improvement in performance. The proposed structures were based on crosslinked polystyrene latex particles, 310 nm in diameter, generated by surfactant-free emulsion polymerization. The particles were chloromethylated and grafted with linear polystyrene chains with a molecular weight of 30,000 g/mol. A second generation support was also prepared with an additional cycle of functionalization and grafting, using 30,000 g/mol side chains and the chloromethylated once-grafted latices. The well-defined particles were functionalized with sulfonic acid and chelating groups. The performance of the sulfonated supports was compared with that of linear polymers and commercial resins in the hydrolysis of methyl acetate. The catalytic activity of the pellicular resins was similar to linear polymers of comparable substitution level. The ligand bis-2-picolylamine was also introduced on the polymer support, for comparison with the commercial Dow chelating macroporous resin XF-4195. The exchange rate obtained for the pellicular resin was much faster than for the commercial resin. The relative importance of structural effects and size effects in improving the performance of the supports could not, however, be determined.
引用
收藏
页码:67 / 79
页数:13
相关论文
共 21 条
[1]  
BERGBREITER DE, 1986, ACS SYM SER, V308, P17
[2]   MECHANISMS OF POLYMER-SUPPORTED CATALYSIS .6. QUATERNARY PHOSPHONIUM IONS ON POLYSTYRENE LATEXES AS CATALYSTS FOR NUCLEOPHILIC DISPLACEMENTS [J].
BERNARD, M ;
FORD, WT ;
TAYLOR, TW .
MACROMOLECULES, 1984, 17 (09) :1812-1814
[3]   ACCESSIBILITY AND CATALYTIC ACTIVITY OF SULFONIC-ACID ION-EXCHANGE RESINS IN DIFFERENT SOLVENTS [J].
BUTTERSACK, C .
REACTIVE POLYMERS, 1989, 10 (2-3) :143-164
[4]  
DEVON MJ, 1991, ACS SYM SER, V472, P154
[5]   MODEL FILLED POLYMERS .9. SYNTHESIS OF UNIFORMLY CROSS-LINKED POLYSTYRENE MICROBEADS [J].
DING, ZY ;
MA, SM ;
KRIZ, D ;
AKLONIS, JJ ;
SALOVEY, R .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1992, 30 (11) :1189-1194
[6]   REACTIVE POLYMERS - DESIGN CONSIDERATIONS, NOVEL PREPARATIONS AND SELECTED APPLICATIONS IN ORGANIC-CHEMISTRY [J].
FRECHET, JMJ ;
DARLING, GD ;
ITSUNO, S ;
LU, PZ ;
DEMEFTAHI, MV ;
ROLLS, WA .
PURE AND APPLIED CHEMISTRY, 1988, 60 (03) :353-364
[7]  
GARROU PE, 1978, Patent No. 4080338
[8]   Arborescent graft copolymers: Highly branched macromolecules with a core-shell morphology [J].
Gauthier, M ;
Tichagwa, L ;
Downey, JS ;
Gao, S .
MACROMOLECULES, 1996, 29 (02) :519-527
[9]   UNIFORM HIGHLY BRANCHED POLYMERS BY ANIONIC GRAFTING - ARBORESCENT GRAFT POLYMERS [J].
GAUTHIER, M ;
MOLLER, M .
MACROMOLECULES, 1991, 24 (16) :4548-4553
[10]  
Goodwin J.W., 1973, POLYM INT, V5, P347