Comparison of the effect of pore architecture and bead size on the extent of plasmachemical amine functionalisation of poly(styrene-codivinylbenzene) permanently porous resins

被引:20
作者
Badyal, JP
Cameron, AM
Cameron, NR
Oates, LJ
Oye, G
Steel, PG
Davis, BG
Coe, DM
Cox, RA
机构
[1] Univ Durham, Dept Chem, Durham DH1 3LE, England
[2] Univ Oxford, Dyson Perrins Lab, Dept Chem, Oxford OX1 3QY, England
[3] GlaxoSmithKline, Med Res Ctr, Stevenage SG1 2NY, Herts, England
基金
英国生物技术与生命科学研究理事会;
关键词
polymer beads; porous; plasmachemistry;
D O I
10.1016/j.polymer.2004.01.072
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(styrene-co-divinylbenzene) (PS/DVB) permanently porous resins suitable for plasmachemical modification with allylamine were prepared by suspension polymerisation. Experimental design methods were employed to investigate simultaneously the influence of crosslinker content, porogen type and porogen level on the surface area, pore volume and pore diameter of the resins. From this, it was found that the porogen has a greater influence than the crosslinker. Variation of porogen type and level while keeping crosslinker level constant then lead to the maximisation of each parameter of interest, resulting in a set of samples with a wide range of values. Six samples were then chosen, representing high and low values of each property, and were subjected to plasmachemical modification with allylamine. It was found that pore volume had the greatest influence on the extent of modification. However, subsequent experiments indicated that the extent of modification is much greater for smaller beads. It is concluded that plasmachemical functionalisation occurs mainly on the external surface of the beads. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2185 / 2192
页数:8
相关论文
共 49 条
[1]   HIGH POROSITY POLYSTYRENE CATION EXCHANGE RESINS [J].
ABRAMS, IM .
INDUSTRIAL AND ENGINEERING CHEMISTRY, 1956, 48 (09) :1469-1472
[2]   THE DETERMINATION OF PORE VOLUME AND AREA DISTRIBUTIONS IN POROUS SUBSTANCES .1. COMPUTATIONS FROM NITROGEN ISOTHERMS [J].
BARRETT, EP ;
JOYNER, LG ;
HALENDA, PP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (01) :373-380
[3]  
Brandrup J., 1999, Polymer handbook, VII
[4]   Adsorption of gases in multimolecular layers [J].
Brunauer, S ;
Emmett, PH ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 :309-319
[5]   Use of a scintillant-containing macroporous resin in both solid phase synthesis and subsequent on-bead scintillation-based analysis [J].
Clapham, B ;
Sutherland, AJ .
TETRAHEDRON LETTERS, 2000, 41 (13) :2257-2260
[6]   STYRENE DIVINYLBENZENE COPOLYMERS - FORMATION OF POROUS STRUCTURE BY USING PRECIPITANTS AS DILUENTS IN SUSPENSION POLYMERIZATION [J].
COUTINHO, FMB ;
CID, RCA .
EUROPEAN POLYMER JOURNAL, 1990, 26 (11) :1185-1188
[7]   COPOLYMERS BASED ON STYRENE AND DIVINYLBENZENE SYNTHESIZED IN THE PRESENCE OF DEPHA .1. STRUCTURAL CHARACTERIZATION [J].
COUTINHO, FMB ;
BARBOSA, CCR ;
REZENDE, SM .
EUROPEAN POLYMER JOURNAL, 1995, 31 (12) :1243-1250
[8]   SCANNING ELECTRON-MICROSCOPY STUDY OF STYRENE DIVINYLBENZENE COPOLYMERS [J].
COUTINHO, FMB ;
RABELO, D .
EUROPEAN POLYMER JOURNAL, 1992, 28 (12) :1553-1557
[9]  
Coutinho FMB, 1997, J APPL POLYM SCI, V65, P1257, DOI 10.1002/(SICI)1097-4628(19970815)65:7<1257::AID-APP3>3.0.CO
[10]  
2-H