Kinetic scheme and rate constants for methyl methacrylate synthesis occurring via the radical–coordination mechanism
Autor: | K. A. Tereshchenko, D. A. Shiyan, S. V. Kolesov, N. E. Temnikova, A. O. Burakova, A. K. Frizen, N. V. Ulitin |
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Rok vydání: | 2017 |
Předmět: |
Kinetic chain length
Nitroxide mediated radical polymerization 010405 organic chemistry Chemistry Radical polymerization Kinetic scheme Chain transfer General Chemistry 010402 general chemistry Photochemistry 01 natural sciences Catalysis 0104 chemical sciences Computer Science Applications Living free-radical polymerization Cobalt-mediated radical polymerization Modeling and Simulation Reversible addition−fragmentation chain-transfer polymerization |
Zdroj: | Kinetics and Catalysis. 58:122-132 |
ISSN: | 1608-3210 0023-1584 |
DOI: | 10.1134/s0023158417020136 |
Popis: | Two kinetic schemes of the bulk radical–coordination polymerization of methyl methacrylate initiated by the benzoyl peroxide–ferrocene system are considered from the standpoint of formal kinetics. The most likely kinetic scheme is the one that includes the reactions characteristic of classical radical polymerization and, additionally, reactions of controlled radical polymerization proceeding via the Organometallic Mediated Radical Polymerization mechanism, a reaction generating a coordination active site, and a chain propagation reaction in the coordination sphere of the metal. The temperature dependences of the rate constants for the reactions of this kinetic scheme at temperatures typical of commercial poly(methyl methacrylate) production (313–353 K) have been determined by solving the inverse kinetic problem. |
Databáze: | OpenAIRE |
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