Preparation of macroporous methacrylate monolithic material with convective flow properties for bioseparation: Investigating the kinetics of pore formation and hydrodynamic performance

被引:39
作者
Danquah, Michael K. [1 ]
Forde, Gareth M. [1 ]
机构
[1] Monash Univ, Dept Chem Engn, BEL Bio Engn Lab, Clayton, Vic 3800, Australia
关键词
methacrylate monolith; macroporous; polymerisation; pore formation; porosity;
D O I
10.1016/j.cej.2008.02.012
中图分类号
X [环境科学、安全科学];
学科分类号
08 [工学]; 0830 [环境科学与工程];
摘要
The preparation of macroporous methacrylate monolithic material with controlled pore structures can be carried out in an unstirred mould through careful and precise control of the polymerisation kinetics and parameters. Contemporary synthesis conditions of methacrylate monolithic polymers are based on existing polymerisation schemes without an in-depth understanding of the dynamics OF pore structure and formation. This leads to poor performance in polymer usage thereby affecting final product recovery and purity, retention time, productivity and process economics. The unique porosity of methacrylate monolithic polymer which propels its usage in many industrial applications can be controlled easily during its preparation. Control of the kinetics of the overall process through changes in reaction time, temperature and overall composition such as cross-linker and initiator contents allow the fine tuning of the macroporous structure and provide an understanding of the mechanism of pore formation within the unstirred mould. The significant effect of temperature of the reaction kinetics serves as an effectual means to control and optimise the pore structure and allows the preparation of polymers with different pore size distributions from the same composition of the polymerisation mixture. Increasing the concentration of the cross-linking monomer affects the composition of the final monoliths and also decreases the average pore size as a result of pre-mature formation of highly cross-linked globules with a reduced propensity to coalesce. The choice and concentration of porogen solvent is also imperative. Different porogens and porogen mixtures present different pore structure output. Example, larger pores are obtained in a poor solvent due to early phase separation. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:593 / 599
页数:7
相关论文
共 10 条
[1]
Brandrup J., 1999, Polymer handbook, VII
[2]
Application of semi-industrial monolithic columns for downstream processing of clotting factor IX [J].
Branovic, K ;
Buchacher, A ;
Barut, M ;
Strancar, A ;
Josic, D .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2003, 790 (1-2) :175-182
[3]
Characterization and modeling of monolithic stationary phases: application to preparative chromatography [J].
Ghose, S ;
Cramer, SM .
JOURNAL OF CHROMATOGRAPHY A, 2001, 928 (01) :13-23
[4]
Guyot A., 1982, PROG POLYM SCI, V8, P277, DOI [10.1016/0079-6700(82)90002-8., DOI 10.1016/0079-6700(82)90002-8]
[5]
REACTIVE POLYMERS .25. MORPHOLOGY OF POLYMERIC SORBENTS BASED ON GLYCIDYL METHACRYLATE COPOLYMERS [J].
PELZBAUER, Z ;
LUKAS, J ;
SVEC, F ;
KALAL, J .
JOURNAL OF CHROMATOGRAPHY, 1979, 171 (APR) :101-107
[6]
Preparation of large-diameter ''molded'' porous polymer monoliths and the control of pore structure homogeneity [J].
Peters, EC ;
Svec, F ;
Frechet, JMJ .
CHEMISTRY OF MATERIALS, 1997, 9 (08) :1898-1902
[7]
Construction of large volume monolithic columns [J].
Podgornik, A ;
Barut, M ;
Strancar, A ;
Josic, D ;
Koloini, T .
ANALYTICAL CHEMISTRY, 2000, 72 (22) :5693-5699
[8]
REAGENTS ON STYRENE DIVINYLBENZENE SUPPORTS WITH IMPROVED ACCESSIBILITY [J].
REVILLON, A ;
GUYOT, A ;
YUAN, Q ;
DAPRATO, P .
REACTIVE POLYMERS, 1989, 10 (01) :11-25
[9]
KINETIC CONTROL OF PORE FORMATION IN MACROPOROUS POLYMERS - FORMATION OF MOLDED POROUS MATERIALS WITH HIGH-FLOW CHARACTERISTICS FOR SEPARATIONS OR CATALYSIS [J].
SVEC, F ;
FRECHET, JMJ .
CHEMISTRY OF MATERIALS, 1995, 7 (04) :707-715
[10]
TEMPERATURE, A SIMPLE AND EFFICIENT TOOL FOR THE CONTROL OF PORE-SIZE DISTRIBUTION IN MACROPOROUS POLYMERS [J].
SVEC, F ;
FRECHET, JMJ .
MACROMOLECULES, 1995, 28 (22) :7580-7582