The two-phase structure of polymer blends or block copolymers prepared with polyurethane macroazo initiators and methyl methacrylate or styrene have been studied. The synthesis of these block copolymers was reported in a previous article (Cheikhalard, et al. J Appl Polym Sci 1998, 70, 613-627). One
Block copolymers derived from 2,2′-azobis(2-cyanopropanol). I. Synthesis of poly(urethane-block-methyl methacrylate) and poly(urethane-block-styrene)
✍ Scribed by Talal Cheikhalard; Valerie Massardier; Lan Tighzert; Jean Pierre Pascault
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 247 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0021-8995
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✦ Synopsis
Block copolymers with polyester-urethane and polymethyl methacrylate (PMMA) or polystyrene (PS) sequences were obtained by the use of polyester-or polyether-urethane macroazo initiators (PUMAI). PUMAI with a well-defined number of azo groups per chain were prepared via a two-stage reaction procedure using 2,2Ј-azobis(2-cyanopropanol) (ACP), 4,4Ј-methylene diphenyl diisocyanate (MDI) and ␣, -hydroxy polycaprolactone (PCL). The characteristics of the obtained block copolymers depend on the reaction conditions, and a yield of 98% was obtained for a P(U-b-MMA) synthesized with a ratio of macroazo initiator to monomer equal to 1/400. In similar conditions, copolymerization of styrene was more difficult, and the maximum block copolymer yield obtained in this work was only of 37% for a ratio of macroazo initiator to monomer equal to 1/150. Combination of different analyses Fourier transform infrared (FTIR) spectroscopy, proton nuclear magnetic resonance ( 1 H-NMR), and size exclusion chromatography (SEC) carried out on both crude and fractionated copolymers showed this kind of synthesis yielding di-and triblock copolymers and only a little amount of PU homopolymer.
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