

The kinetics of styrene-free radical bulk polymerization was studied by differential scanning calorimetry (DSC). The data obtained from DSC thermograms were used to model and predict the autoacceleration during styrene polymerization and to understand how it is influenced by temperature. The experimental data were well described by the estimated kinetic model. The model included two processes (the first-order reaction and autoacceleration), because they occur simultaneously as two parallel reactions rather than being strictly separated. It was found that the autoacceleration activation energy is approximately four times lower than the energy of the first-order reaction. In addition, the first-order reaction followed by the autoacceleration of the styrene-free radical bulk polymerization occurs simultaneously only between 41.7 and 110.5 °C. © The Society of Polymer Science, Japan (SPSJ) All rights reserved.
| Engineering uncontrolled terms | AutoaccelerationBulk polymerizationExperimental dataFirst order reactionsKinetic modelingKinetic modelsParallel reactionspolymerization kineticsStyrene polymerizationStyrene-free radicals |
|---|---|
| Engineering controlled terms: | Activation energyDifferential scanning calorimetryFree radicalsKinetic theoryKineticsPolymersPolystyrenesStyrene |
| Engineering main heading: | Free radical polymerization |
| Funding sponsor | Funding number | Acronym |
|---|---|---|
| Ministarstvo Prosvete, Nauke i Tehnološkog Razvoja | 45022 | MPNTR |
We express our gratitude to the Ministry of Science and Technological Development of the Republic of Serbia for providing financial support for this study (Project No. 45022).
Bera, O.; Department of Materials Engineering, Faculty of Technology, University of Novi Sad, Bulevar cara Lazara 1, Serbia;
© Copyright 2011 Elsevier B.V., All rights reserved.