Modeling methyl methacrylate free radical polymerization in nanoporous confinement

被引:31
作者
Begum, Fatema [1 ]
Simon, Sindee L. [1 ]
机构
[1] Texas Tech Univ, Dept Chem Engn, Lubbock, TX 79409 USA
基金
美国国家科学基金会;
关键词
PMMA; Free radical polymerization; Nanoconfinement; DIFFUSION-CONTROLLED TERMINATION; CONTROLLED VINYL POLYMERIZATION; GLASS-TRANSITION TEMPERATURE; M DICYANATE ESTER; THIN-FILMS; RELAXATION DYNAMICS; ALUMINUM POWDERS; MOLECULAR-WEIGHT; SOLVENT SYSTEMS; HIGH CONVERSION;
D O I
10.1016/j.polymer.2011.02.009
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Nanoconfinement of methyl methacrylate free radical polymerization is known to impact the molecular weight and molecular weight distribution of the polymer produced, with results in the literature generally indicating an increase in molecular weight and a concomitant decrease in polydispersity index. In the present work, the mathematical model described by Verros et al. (2005) for free radical bulk polymerization of methyl methacrylate is extended to account for polymerization in nanopores. The model of Verros et al. (2005) incorporates diffusion effects and is capable of describing the conversion and the number- and weight-average molecular weights of the resulting poly(methyl methacrylate) as a function of polymerization time and process conditions. The model is extended by incorporating the effect of nanoconfinement on diffusivity using the scaling reported in the literature. The calculations indicate that nanoconfinement will lead to higher molecular weights and lower polydispersity, and the gel effect will occur earlier. The results are compared to experimental work and implications discussed. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1539 / 1545
页数:7
相关论文
共 60 条
[1]   MODELING OF DIFFUSION-CONTROLLED FREE-RADICAL POLYMERIZATION REACTIONS [J].
ACHILIAS, D ;
KIPARISSIDES, C .
JOURNAL OF APPLIED POLYMER SCIENCE, 1988, 35 (05) :1303-1323
[2]   DEVELOPMENT OF A GENERAL MATHEMATICAL FRAMEWORK FOR MODELING DIFFUSION-CONTROLLED FREE-RADICAL POLYMERIZATION REACTIONS [J].
ACHILIAS, DS ;
KIPARISSIDES, C .
MACROMOLECULES, 1992, 25 (14) :3739-3750
[3]   OXIDATION BEHAVIOR OF ALUMINUM NANOPOWDERS [J].
AUMANN, CE ;
SKOFRONICK, GL ;
MARTIN, JA .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY B, 1995, 13 (03) :1178-1183
[4]   Polymer chains in a soft nanotube: A Monte Carlo Study [J].
Avramova, K ;
Milchev, A .
JOURNAL OF CHEMICAL PHYSICS, 2006, 124 (02)
[5]   BULK POLYMERIZATION OF METHYL-METHACRYLATE [J].
BALKE, ST ;
HAMIELEC, AE .
JOURNAL OF APPLIED POLYMER SCIENCE, 1973, 17 (03) :905-949
[6]  
Beers KJ, 2007, NUMERICAL METHODS FOR CHEMICAL ENGINEERING: APPLICATIONS IN MATLAB, P1
[7]   Critically evaluated rate coefficients for free-radical polymerization .2. Propagation rate coefficients for methyl methacrylate [J].
Beuermann, S ;
Buback, M ;
Davis, TP ;
Gilbert, RG ;
Hutchinson, RA ;
Olaj, OF ;
Russell, GT ;
Schweer, J ;
vanHerk, AM .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 1997, 198 (05) :1545-1560
[8]   BULK THERMAL COPOLYMERIZATION OF STYRENE P-METHYLSTYRENE - MODELING DIFFUSION-CONTROLLED TERMINATION AND PROPAGATION USING FREE-VOLUME THEORY [J].
BHATTACHARYA, D ;
HAMIELEC, AE .
POLYMER, 1986, 27 (04) :611-618
[9]  
Billmeyer F.W., 1984, TXB POLYM SCI
[10]   Examination of the influence of cooperative segmental dynamics on the glass transition and coefficient of thermal expansion in thin films probed using poly(n-alkyl methacrylate)s [J].
Campbell, Casey G. ;
Vogt, Bryan D. .
POLYMER, 2007, 48 (24) :7169-7175