1985
DOI: 10.1002/app.1985.070301004
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Modeling the free radical solution and bulk polymerization of methyl methacrylate

Abstract: SynopsisThis paper reviews our current understanding of the kinetics and mechanisms of free-radical chain polymerization of methyl methacrylate. A mathematical model previously proposed to describe the bulk polymerization of MMA is here extended to cover solution polymerization. This extended model is validated by comparing its predictions with experimental data over a range of conversions and product molecular weights.

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Cited by 104 publications
(85 citation statements)
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“…Termination is by combination or disproportionation reactions. With chain transfer reactions to monomer, initiator, solvent, or even polymer, the active free radicals are converted to dead polymer [1]. …”
Section: Polymerization Mechanismmentioning
confidence: 99%
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“…Termination is by combination or disproportionation reactions. With chain transfer reactions to monomer, initiator, solvent, or even polymer, the active free radicals are converted to dead polymer [1]. …”
Section: Polymerization Mechanismmentioning
confidence: 99%
“…k p  and t  are adjustable parameters related to propagation and termination rate constants, respectively. All the other necessary parameters and constants for this model are given in the literature [1]. The Equations (7)-(10) are essential for dynamic studies.…”
Section: Mathematical Modeling Of Polymerizationmentioning
confidence: 99%
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“…Number of equations can be reduced to finite numbers by moments. Definitions of moments are (Louie et al (1985)): Table 2 shows the governing equations. The polymer production in this reaction is accomplished with reduction in the mixture volume.…”
Section: Mathematical Modelingmentioning
confidence: 99%
“…For the parameter estimation a constant reaction volume was assumed (P=Oo). Louie et al (1985) this study this study Since the purpose of the kinetics study is the modelling of the reactive extrusion, it is necessary, to take into account the axial temperature profile in the reactor. The kinetics model was therefore compared with experimental results obtained under non-isothermal conditions.…”
Section: -E I With K I =Aiexp(--r-f-imentioning
confidence: 99%