ChemInform Abstract: SYNTHESIS OF BLOCK COPOLYMERS OF VINYL ACETATE AND ETHYL ACRYLATE BY TELOMERIZATION

1978 ◽  
Vol 9 (47) ◽  
Author(s):  
B. BOUTEVIN ◽  
M. MACRET ◽  
C. MAUBERT ◽  
Y. PIETRASANTA ◽  
M. TANESIE
2010 ◽  
Vol 211 (15) ◽  
pp. 1678-1688 ◽  
Author(s):  
Nick Fandrich ◽  
Jana Falkenhagen ◽  
Steffen M. Weidner ◽  
Bastiaan Staal ◽  
Andreas F. Thünemann ◽  
...  

2020 ◽  
Vol 138 (14) ◽  
pp. 50151
Author(s):  
Houjian Gong ◽  
Wenyu Gui ◽  
Hao Zhang ◽  
Wei Lv ◽  
Long Xu ◽  
...  

2013 ◽  
Vol 66 (12) ◽  
pp. 1564 ◽  
Author(s):  
Lily A. Dayter ◽  
Kate A. Murphy ◽  
Devon A. Shipp

A single reversible addition–fragmentation chain transfer (RAFT) agent, malonate N,N-diphenyldithiocarbamate (MDP-DTC) is shown to successfully mediate the polymerization of several monomers with greatly differing reactivities in radical/RAFT polymerizations, including both vinyl acetate and styrene. The chain transfer constants (Ctr) for MDP-DTC for both these monomers were evaluated; these were found to be ~2.7 in styrene and ~26 in vinyl acetate, indicating moderate control over styrene polymerization and good control of vinyl acetate polymerization. In particular, the MDP-DTC RAFT agent allowed for the synthesis of block copolymers of these two monomers without the need for protonation/deprotonation switching, as has been previously developed with N-(4-pyridinyl)-N-methyldithiocarbamate RAFT agents, or other end-group transformations. The thermal properties of the block copolymers were studied using differential scanning calorimetry, and those with sufficiently high molecular weight and styrene composition appear to undergo phase separation. Thus, MDP-DTC may be useful for the production of other block copolymers consisting of monomers with highly dissimilar reactivities.


1993 ◽  
Vol 50 (4) ◽  
pp. 279-286 ◽  
Author(s):  
Kazutoshi TERADA ◽  
Hirotoshi MIYAZAKI ◽  
Mototsugu YOSHIHARA ◽  
Toshiaki SATO ◽  
Hitoshi MARUYAMA ◽  
...  

2009 ◽  
Vol 1239 ◽  
Author(s):  
Eric Allen Eastwood ◽  
Daniel Edward Bowen ◽  
Mark W. Lee

AbstractA wide variety of nanofillers of varying compositions have been used to create polymer nanocomposites, including tubes, wires, fibers, sheets, and particles. A new class of compounds has been identified for use as nanofillers, boron cage compounds. Boron cage compounds are discrete, icosahedral closed cage molecules of high boron content and examples include carboranes and dodecaborate salts. Several chemically modified boron cage compounds have been incorporated into polyolefin elastomers, such as poly(ethylene-co-vinyl acetate), poly(ethylene-co-vinyl acetate-co-vinyl alcohol), poly(ethylene-co-ethyl acrylate), and poly(ethylene-co-octene), among others. The resulting thermal and thermomechanical properties were evaluated in order to determine when plasticization and reinforcement occur to better understand the chemical structure/physical property relationships. Materials with a wide range of properties were produced, however under certain conditions, advanced materials were created with high boron contents, improved thermal stability, mechanical strength, and significant reinforcement.


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