Effect of the addition of inert or TEMPO‐capped prepolymer on polymerization rate and molecular weight development in the nitroxide‐mediated radical polymerization of styrene

2008 ◽  
Vol 109 (6) ◽  
pp. 3665-3678 ◽  
Author(s):  
Martha Roa‐Luna ◽  
Afsaneh Nabifar ◽  
Neil T. McManus ◽  
Eduardo Vivaldo‐Lima ◽  
Liliane M. F. Lona ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Radical Polymerization ◽  
Polymerization Rate

Assessing the Importance of Diffusion‐Controlled Effects on Polymerization Rate and Molecular Weight Development in Nitroxide‐Mediated Radical Polymerization of Styrene

2007 ◽  
Vol 44 (2) ◽  
pp. 193-203 ◽  
Author(s):  
Martha Roa‐Luna ◽  
Martha Patricia Díaz‐barber ◽  
Eduardo Vivaldo‐Lima ◽  
Liliane M.F. Lona ◽  
Neil T. McManus ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Radical Polymerization ◽  
Polymerization Rate ◽  
Diffusion Controlled

Effect of initiator type and concentration on polymerization rate and molecular weight in the bimolecular nitroxide-mediated radical polymerization of styrene

2010 ◽  
Vol 29 (1) ◽  
pp. 11-19 ◽  
Author(s):  
Telma Regina Nogueira ◽  
Maria Cecília Gonçalves ◽  
Liliane Maria Ferrareso Lona ◽  
Eduardo Vivaldo-Lima ◽  
Neil McManus ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Radical Polymerization ◽  
Polymerization Rate

Tertiary amine catalyzed photo-induced controlled radical polymerization of methacrylates

2015 ◽  
Vol 6 (30) ◽  
pp. 5362-5368 ◽  
Author(s):  
Qiang Fu ◽  
Thomas G. McKenzie ◽  
Shereen Tan ◽  
Eunhyung Nam ◽  
Greg G. Qiao
Keyword(s):  
Molecular Weight ◽  
Radical Polymerization ◽  
Uv Irradiation ◽  
Tertiary Amine ◽  
Controlled Radical Polymerization ◽  
Low Molecular Weight ◽  
Molecular Weight Distributions ◽  
Weight Distributions ◽  
End Group

A novel tertiary amine catalyst and trithiocarbonate synergistic photo-induced controlled radical polymerization of methacrylates has been realized under mild UV irradiation, yielding polymethacrylates with low molecular weight distributions and excellent end-group fidelity.

scholarly journals Effect of Ferocene Concentration on the Percent Conversion and Molecular Weight of Poly(Methyl Methacrylate) Homopolymers

2017 ◽  
Vol 14 (2) ◽  
pp. 311-319
Author(s):  
Baghdad Science Journal
Keyword(s):  
Molecular Weight ◽  
Free Radical ◽  
Methyl Methacrylate ◽  
Benzoyl Peroxide ◽  
Radical Polymerization ◽  
Free Oxygen ◽  
Poly Methyl Methacrylate ◽  
Methacrylate Monomer ◽  
Percent Conversion ◽  
Methyl Methacrylate Monomer

This research is addressing the effect of different ferrocene concentration (0.00, 2.15x10-3, 4.30x10-3, 8.60x10-3, and 12.9x10-3) on the bulk free radical polymerization of methyl methacrylate monomer in benzene using benzoyl peroxide as initiator. The polymerization was conducted at 60º C under free oxygen atmosphere. The resulting polymers were characterized by FTIR. The results were compared with the presence and absence of ferrocene at 10% conversion. The %conversion was 3.04% with no ferrocene present in the polymerization medium and its increase to 9.06 with a first lowest ferrocene concentration added, i.e. 2.15 x10-3mol/l. This was positively reflected on the poly(methyl methacrylate) molecular weight measured by viscosity technique, especially in the presence of ferrocene.

The Kinetics of Free-Radical Polymerization: Fundamental Aspects

2002 ◽  
Vol 55 (7) ◽  
pp. 399 ◽  
Author(s):  
G. T. Russell
Keyword(s):  
Molecular Weight ◽  
Steady State ◽  
Free Radical ◽  
Radical Polymerization ◽  
Chain Length ◽  
Free Radical Polymerization ◽  
Length Dependence ◽  
Model Independent ◽  
Living Free Radical Polymerization ◽  
Kinetics Of

Some fundamental aspects of the kinetics of free-radical polymerization are reviewed. So-called classical results for rate and molecular-weight distribution are first of all presented. It is shown how this approach can be built upon when chain-length-dependent termination is allowed, which it always should be. Various termination models are considered, and it is illustrated that although the models are different, rather remarkably they give common, model-independent behaviour. Some leading experimental results regarding the chain-length dependence of termination are summarized, before the chain-length dependence of other reactivities, the variation of reactivities with conversion, and non-steady state experiments are briefly discussed. Finally, living free-radical polymerization as effected by a reversible termination agent is considered. An outline of the kinetics of these systems is given, with the oft-neglected importance of conventional termination being stressed.

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