A theoretical investigation of the production of branched copolymers in continuous stirred tank reactors

✍ Scribed by Apostolis Baltsas; Dimitris S. Achilias; Costas Kiparissides

• Publisher: John Wiley and Sons
• Year: 1996
• Tongue: English
• Weight: 811 KB
• Volume: 5
• Category: Article
• ISSN: 1022-1344
• DOI: 10.1002/mats.1996.040050307

✦ Synopsis

Abstract

A comprehensive mathematical model for free‐radical copolymerization reactions has been developed for a homogeneous continuous stirred tank reactor. The present model is based on a fairly general copolymerization scheme accounting for the formation of linear and branched copolymer chains. Both chain transfer to polymer and terminal double bond reactions are considered in order to predict the long chain branching frequency. Changes in molecular weight, composition and degree of branching occurring during the copolymerization reaction are modelled using the method of moments. To break‐down the dependence of the moment equations on higher order moments two different closure methods are considered. The predictive capabilities of the model are examined in relation to the solution copolymerization of methyl methacrylate with vinyl acetate. It is shown that both chain transfer to polymer and terminal double bond reactions significantly contribute to the broadening of the molecular weight and degree of branching distributions. Furthermore, the terminal double bond reaction effects significantly the copolymer number‐average molecular weight and the concentration of terminal double bonds.