## Abstract A penultimate model of acrylate polymerization has been proposed to account for reduced reactivity of radicals formed by monomer addition to midchain radicals. New expressions derived for polymerization rate, number‐average degree of polymerization and branching level are used for a com
The Effect of Intramolecular Transfer to Polymer on Stationary Free-Radical Polymerization of Alkyl Acrylates, 3 – Consideration of Solution Polymerization up to High Conversions
✍ Scribed by Anatoly N. Nikitin; Robin A. Hutchinson; George A. Kalfas; John R. Richards; Christopher Bruni
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 361 KB
- Volume
- 18
- Category
- Article
- ISSN
- 1022-1344
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✦ Synopsis
Abstract
The kinetics of butyl acrylate solution polymerization up to high conversion are studied both experimentally and theoretically. New expressions taking into account both inter‐ and intra‐molecular transfer to polymer are derived for polymerization rate, average chain‐length and branching level. These expressions are used for comparative analysis of these two chain transfer events and for evaluation of the backbiting rate coefficient, k~bb~, and the constant of chain transfer to solvent (xylene), C~trS~. Using batch experiments performed at 50, 60 and 70 °C, the Arrhenius parameters for k~bb~ and C~trS~ are estimated to be, respectively, A(k~bb~) = (7.4 ± 1.5) × 10^7^ s^−1^, E~a~(k~bb~) = (32.7 ± 0.5) kJ · mol^−1^ and A(C~trS~) = 10.5 ± 3.5, E~a~(C~trS~) = (26.9 ± 1.9) kJ · mol^−1^.
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📜 SIMILAR VOLUMES
## Abstract **Summary:** Procedures are developed to estimate kinetic rate coefficients from available rate data for the free radical solution polymerization of butyl acrylate at 50 °C. The analysis is based upon a complete mechanistic set that includes the formation of mid‐chain radicals through b