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Dependence of Propagation Rate Coefficients in Radical Polymerization on Solution Properties
Author(s) -
Deglmann Peter,
Hungenberg KlausDieter,
Vale Hugo M.
Publication year - 2017
Publication title -
macromolecular reaction engineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.37
H-Index - 32
eISSN - 1862-8338
pISSN - 1862-832X
DOI - 10.1002/mren.201600037
Subject(s) - monomer , polymerization , chemistry , radical polymerization , polymer chemistry , styrene , solvent , acrylic acid , thermodynamics , methyl methacrylate , activity coefficient , organic chemistry , polymer , copolymer , aqueous solution , physics
The effect of solvents and monomer concentration on rate coefficients of propagation in radical polymerization has received tremendous interest during recent years, but a quantitative explanation and method of prediction of the medium effect is still missing. In this paper, it is shown that the thermodynamic formulation of the transition state theory is able to explain such effects almost quantitatively for a wide variety of monomers and solvents, including not only organic solvents but also less common solvents like ionic liquids or water, and monomers ranging from styrene to water‐soluble monomers like acrylic acid or N ‐vinylformamide and also bulky monomers like isobornyl methacrylate. The medium effect is dictated by the activity coefficient of the monomer as well as by the ratio of the activity coefficients of the growing chain and the transition state. The solvent and concentration effects are, thus, a consequence of the degree of nonideality of the system. This interpretation based on the thermodynamics of real solutions offers for the first time a straightforward method to estimate the propagation rate coefficient of a given monomer in various solvents once the corresponding coefficient in bulk monomer is known.