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End‐group modification of poly(2,6‐dimethyl‐1,4‐phenylene ether) and in situ synthesis of poly(2,6‐dimethyl‐1,4‐phenylene ether)‐b‐poly(ethylene terephthalate) block copolymer
Authors:Stéphane Jéol  Françoise Fenouillot  Alain Rousseau  Christiane Monnet  Karine Masenelli‐Varlot  Jean‐François Briois
Affiliation:1. RHODIA Opération, Centre de Recherches et Technologies de Lyon, 85 Rue des frères Perret, 69 192 Saint‐Fons, France;2. Université Lyon 1‐IMP/LMM Laboratoire des Matériaux Macromoléculaires, Ingénierie des Matériaux Polymères, UMR CNRS 5223 INSA‐Lyon, 17 Avenue Jean Capelle, F‐69621 Villeurbanne Cedex, France;3. Université Lyon 1‐MATEIS, UMR‐CNRS 5510, INSA‐Lyon, 20 Avenue A. Einstein, F‐69621 Villeurbanne Cedex, France;4. Tergal Industries, Rue Jules Vercruysse, BP 1, 02430 Gauchy, France
Abstract:The preparation of poly(2,6‐dimethyl‐1,4‐phenylene ether)‐b‐poly(ethylene terephthalate) block copolymer was performed by the reaction of the 2‐hydroxyethyl modified poly(2,6‐dimethyl‐1,4‐phenylene ether) (PPE‐EtOH) with poly(ethylene terephthalate) (PET) by an in situ process, during the synthesis of the polyester. The yield of the reaction of the 2‐hydroxyethyl functionalized PPE‐EtOH with PET was close to 100%. A significant proportion of the PET‐b‐PPE‐EtOH block copolymer was found to have short PET block. Nevertheless, the copolymer structured in the shape of micelles (20 nm diameter) and very small domains with 50–200 nm diameter, whereas unmodified PPE formed much larger domains (1.5 μm) containing copolymer. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 3985–3991, 2008
Keywords:block copolymers  compatibilization  poly(ethylene terephthalate)  poly(2,6‐dimethyl‐1,4‐phenylene ether)  polyesters
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