Kinetic investigations of reversible addition fragmentation chain transfer polymerizations: Cumyl phenyldithioacetate mediated homopolymerizations of styrene and methyl methacrylate

Barner-Kowollik, C., Quinn, J. F., Nguyen, T. L. U., Heuts, J. P. A., & Davis, T. P. (2001) Kinetic investigations of reversible addition fragmentation chain transfer polymerizations: Cumyl phenyldithioacetate mediated homopolymerizations of styrene and methyl methacrylate. Macromolecules, 34(22).

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Abstract

A previously published simulation and data fitting procedure for the reversible addition fragmentation chain transfer (RAFT) process using the PREDICI simulation program has been extended to cumyl phenyldithioacetate mediated styrene and methyl methacrylate (MMA) bulk homopolymerizations. The experimentally obtained molecular weight distributions (MWDs) for the styrene system are narrow and unimodal and shift linearly with monomer conversion to higher molecular weights. The MMA system displays a hybrid of conventional chain transfer and living behavior, leading to bimodal MWDs. The styrene system has been subjected to a combined experimental and modeling study at 60 °C, yielding a rate coefficient for the addition reaction of free macroradicals to polymeric RAFT agent, kβ, of approximately 5.6 × 105 L mol-1 s-1 and a decomposition rate coefficient for macroradical RAFT species, k-β, of about 2.7 × 10-1 s-1. The transfer rate coefficient to cumyl phenyldithioacetate is found to be close to 2.2 × 105 L mol-1 s-1. The MMA system has been studied over the temperature range 25-60 °C. The hybrid behavior observed in the MMA polymerizations has been exploited (at low monomer conversions) to perform a Mayo analysis allowing the determination of the temperature dependence of the transfer to cumyl phenyldithioacetate reaction. The activation energy of this process is close to 26 kJ mol-1. In contrast to the styrene system, the PREDICI simulation procedure cannot be successfully applied to cumyl phenyldithioacetate mediated MMA polymerizations for the deduction of kβ and k-β. This inability is due to the hybrid nature of the cumyl phenyldithioacetate-MMA system, leading to a significantly reduced sensitivity toward kβ and k-β.

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ID Code: 99046
Item Type: Journal Article
Refereed: Yes
Additional Information: Cited By :290
Export Date: 5 September 2016
CODEN: MAMOB
Correspondence Address: Davis, T.P.; Ctr. for Advd. Macromolecular Design, Sch. of Chem. Eng./Indust. Chemistry, University of New South Wales, Sydney, NSW 2052, Australia
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Keywords: Reversible addition fragmentation chain transfer (RAFT) process, Activation energy, Computer simulation, Homopolymerization, Molecular weight, Monomers, Polymethyl methacrylates, Styrene
DOI: 10.1021/ma010349m
ISSN: 00249297
Divisions: Current > Schools > School of Chemistry, Physics & Mechanical Engineering
Current > Institutes > Institute for Future Environments
Current > QUT Faculties and Divisions > Science & Engineering Faculty
Deposited On: 22 Sep 2016 04:50
Last Modified: 22 Sep 2016 04:50

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