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Synthesis by radical polymerization

We synthesized [13] IPNs composed of polyethylene oxide) (PEO) (polymer A) and poly(N-acryloylpyrrolidine) (PAPy) (polymer B). The IPN was synthesized by simultaneous crosslinked polymerization of APy and PEO. The overall reaction scheme for IPN synthesis by radical polymerization for APy (polymer A) and addition polymerization for PEO (polymer B) is shown in Fig. 3. This pair shows simple coacervation behavior in water. The IPN is constructed from PEO and PAPy networks as shown in Fig. 4. Chemically independent networks of polymer A and polymer B are interlocked and macroscopic phase separation in water swollen states is avoided. [Pg.184]

G.L. Wilkes, Synthesis of Novel Polymers with Unusual Properties by Radical Polymerization , USARO Rept, Contract DA-ARO-D-31-124-73-G27, Princeton Univ, Princeton (1974)... [Pg.824]

Amiduri, B Boutevin, B. and Gramain, P Synthesis of Block Copolymers by Radical Polymerization and Telomerization. VoL 127, pp. 87-142. [Pg.206]

The incorporation of four different classes of important ultraviolet stabilizers into high polymer chains has been accomplished by synthesis of polymerizable, vinyl-substituted stabilizer derivatives followed by radical polymerization. [Pg.50]

The synthesis of some multiblock copolymers was attempted by successive polymerization using this iniferter technique. However, pure tri- or tetrablock copolymers free from homopolymers were not isolated by solvent extraction because no suitable solvent was found for the separation. In 1963, Merrifield reported a brilliant solid-phase peptide synthesis using a reagent attached to the polymer support. If a similar idea can be applied to the iniferter technique, pure block copolymer could be synthesized by radical polymerization. The DC group attached to a polystyrene gel (PSG) through a hydrolyzable ester spacer was prepared and used as a PSG photoiniferter (Eq. 53) [186] ... [Pg.106]

Since PTFE was first synthesized more than 50 years ago, fluoropolymers have been produced by radical polymerization and copolymerizaton processes, but without any functional groups, for several reasons. First, the synthesis of functional vinyl compounds suitable for radical polymerization is much more complicated and expensive in comparison with common fluoroolefins. In radical polymerization of one of the simplest possible candidates—perfluorovinyl sulfonic acid (or sulfonyl fluoride—there was not enough reactivity to provide high-molecular-weight polymers or even perfluorinated copolymers with considerable functional comonomer content. Several methods for the synthesis of the other simplest monomer—trifluoroacrylic acid or its esters—were reported,1 but convenient improved synthesis of these compounds as well as radical copolymerization with TFE induced by y-irradiation were not described until 1980.2... [Pg.92]

Shi, Z. Q. and Holdcroft, S. 2004. Synthesis of block copolymers possessing fluoropolymer and nonfluoropolymer segments by radical polymerization. [Pg.182]

Undin J, Plikk P, Finne-Wistrand A, Albertsson A-C (2010) Synthesis of amorphous aliphatic polyester-ether homo- and copolymers by radical polymerization of ketene acetals. J Polym Sci A Polym Chem 48 4965 973... [Pg.208]

Synthesis of Block Copolymers by Radical Polymerization and Telomerization... [Pg.87]


See other pages where Synthesis by radical polymerization is mentioned: [Pg.121]    [Pg.126]    [Pg.21]    [Pg.121]    [Pg.126]    [Pg.21]    [Pg.108]    [Pg.2]    [Pg.288]    [Pg.53]    [Pg.623]    [Pg.254]    [Pg.20]    [Pg.4]    [Pg.4]    [Pg.87]    [Pg.87]    [Pg.91]   
See also in sourсe #XX -- [ Pg.214 , Pg.215 , Pg.216 , Pg.217 , Pg.218 , Pg.219 , Pg.220 , Pg.221 ]




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