scholarly journals Origins and Development of Initiation of Free Radical Polymerization Processes

2009 ◽  
Vol 2009 ◽  
pp. 1-10 ◽  
Author(s):  
Dietrich Braun

At present worldwide about 45% of the manufactured plastic materials and 40% of synthetic rubber are obtained by free radical polymerization processes. The first free radically synthesized polymers were produced between 1910 and 1930 by initiation with peroxy compounds. In the 1940s the polymerization by redox processes was found independently and simultaneously at IG Farben in Germany and ICI in Great Britain. In the 1950s the systematic investigation of azo compounds as free radical initiators followed. Compounds with labile C–C-bonds were investigated as initiators only in the period from the end of the 1960s until the early 1980s. At about the same time, iniferters with cleavable S–S-bonds were studied in detail. Both these initiator classes can be designated as predecessors for “living” or controlled free radical polymerizations with nitroxyl-mediated polymerizations, reversible addition fragmentation chain transfer processes (RAFT), and atom transfer radical polymerizations (ATRP).

1998 ◽  
Vol 31 (16) ◽  
pp. 5559-5562 ◽  
Author(s):  
John Chiefari ◽  
Y. K. (Bill) Chong ◽  
Frances Ercole ◽  
Julia Krstina ◽  
Justine Jeffery ◽  
...  

2016 ◽  
Vol 12 ◽  
pp. 2378-2389 ◽  
Author(s):  
Judita Britner ◽  
Helmut Ritter

The first detailed study on free-radical polymerization, copolymerization and controlled radical polymerization of the cyclic push–pull-type monomer methylenelactide in comparison to the non-cyclic monomer α-acetoxyacrylate is described. The experimental results revealed that methylenelactide undergoes a self-initiated polymerization. The copolymerization parameters of methylenelactide and styrene as well as methyl methacrylate were determined. To predict the copolymerization behavior with other classes of monomers, Q and e values were calculated. Further, reversible addition fragmentation chain transfer (RAFT)-controlled homopolymerization of methylenelactide and copolymerization with N,N-dimethylacrylamide was performed at 70 °C in 1,4-dioxane using AIBN as initiator and 2-(((ethylthio)carbonothioyl)thio)-2-methylpropanoic acid as a transfer agent.


e-Polymers ◽  
2007 ◽  
Vol 7 (1) ◽  
Author(s):  
Peng Liu

AbstractModification of polymeric materials has been a significant issue over last two decades in many fields of application. Among modification techniques developed to date, surface grafting has emerged as a simple, useful, and versatile approach to improve surface properties of polymers for a wide variety of applications. The synthesis of tethered block copolymer brushes via the use of controlled/”living” free radical polymerization techniques presents many significant advantages over traditional free radical polymerization techniques. This review surveys recent literature on polymer surfaces with graft chains, mainly focusing on grafting methods such as surface-initiated controlled/”living” free radical polymerization via atom transfer radical polymerization (ATRP), nitroxide-mediated radical polymerization (NMRP), reversible addition fragmentation transfer (RAFT) polymerization and iniferter techniques.


2004 ◽  
Vol 37 (17) ◽  
pp. 6329-6339 ◽  
Author(s):  
Elena Chernikova ◽  
Andrey Morozov ◽  
Ekaterina Leonova ◽  
Elizaveta Garina ◽  
Vladimir Golubev ◽  
...  

2000 ◽  
Vol 49 (9) ◽  
pp. 993-1001 ◽  
Author(s):  
Graeme Moad ◽  
John Chiefari ◽  
(Bill) Y?K Chong ◽  
Julia Krstina ◽  
Roshan T?A Mayadunne ◽  
...  

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