Telechelic Diiodopoly(VDF-co-PMVE) Copolymers by Iodine Transfer Copolymerization of Vinylidene Fluoride (VDF) with Perfluoromethyl Vinyl Ether (PMVE)†

2010 ◽  
Vol 43 (8) ◽  
pp. 3652-3663 ◽  
Author(s):  
Cyrille Boyer ◽  
Bruno Ameduri ◽  
Ming H. Hung
Author(s):  
Florian Brandl ◽  
Jan Schwaderer ◽  
Marco Drache ◽  
Sabine Beuermann

2016 ◽  
Vol 7 (39) ◽  
pp. 6099-6109 ◽  
Author(s):  
Sanjib Banerjee ◽  
Saad Zaghloul ◽  
Ali Alaaeddine ◽  
Bruno Ameduri

ω-Hydroxy functionalized poly(vinylidene fluoride) prepared in a water-based non-fluorinated solvent by iodine transfer copolymerization VDF and 1234yf.


2011 ◽  
Vol 44 (5) ◽  
pp. 1114-1124 ◽  
Author(s):  
Hideo Sawada ◽  
Tsukasa Tashima ◽  
Yusuke Nishiyama ◽  
Mieko Kikuchi ◽  
Yuki Goto ◽  
...  

1974 ◽  
Vol 47 (2) ◽  
pp. 282-284 ◽  
Author(s):  
A. B. Kryukova ◽  
A. S. Kuz'minskii ◽  
N. S. Gilinskaya ◽  
F. A. Galil-Ogly ◽  
G. A. Sankina

Abstract Rates of radiation chemical crosslinking and scission of fluorine containing elastomers based on copolymers of vinylidene fluoride with trifluorochloroethylene (Copolymer 1), with hexafluoropropylene (Copolymer 2), and with a perfluoroalkyl vinyl ether (Copolymer 3) and also the behavior of their radiation vulcanizates in the stressed state at high temperatures are determined both by the type of polymer and by the irradiation conditions. Crosslinking rates of Copolymers 2 and 3 are higher than those of Copolymer 1; oxygen of the air inhibits crosslinking by γ-radiation; by irradiation in the presence of oxygen of the air, the sol fraction is 8–10 times higher than in its absence, Copolymer 3 vulcanizates obtained by irradiation in the absence of air appear to be optimal.


Polymers ◽  
2018 ◽  
Vol 10 (9) ◽  
pp. 1008 ◽  
Author(s):  
Florian Brandl ◽  
Marco Drache ◽  
Sabine Beuermann

Semi-batch emulsion polymerizations of vinylidene fluoride (VDF) are reported. The molar mass control is achieved via iodine transfer polymerization (ITP) using IC4F8I as chain transfer agent. Polymerizations carried out at 75 °C and pressures ranging from 10 to 30 bar result in low dispersity polymers with respect to the molar mass distribution (MMD). At higher pressures a significant deviation from the ideal behavior expected for a reversible deactivation transfer polymerization occurs. As identified by kinetic Monte Carlo (kMC) simulations of the activation–deactivation equilibrium, during the initialization period of the chain transfer agent already significant propagation occurs due to the higher pressure, and thus, the higher monomer concentration available. Based on the kMC modeling results, semi-batch emulsion polymerizations were carried out as a two pressure process, which resulted in very good control of the MMD associated with a comparably high polymerization rate.


2006 ◽  
Vol 44 (19) ◽  
pp. 5763-5777 ◽  
Author(s):  
Cyrille Boyer ◽  
David Valade ◽  
Patrick Lacroix-Desmazes ◽  
Bruno Ameduri ◽  
Bernard Boutevin

2005 ◽  
Vol 38 (25) ◽  
pp. 10353-10362 ◽  
Author(s):  
Cyrille Boyer ◽  
David Valade ◽  
Laurent Sauguet ◽  
Bruno Ameduri ◽  
Bernard Boutevin

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