Home Poly(ethylene-co-butylene)-b-(styrene-ran-maleic anhydride)2 Compatibilizers via Nitroxide Mediated Radical Polymerization
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Poly(ethylene-co-butylene)-b-(styrene-ran-maleic anhydride)2 Compatibilizers via Nitroxide Mediated Radical Polymerization

  • B. Lessard , C. Aumand-Bourque , R. Chaudury , D. Gomez , A. Haroon , N. Ibrahimian , S. Mackay , M.-C. Noel , R. Patel , S. Sitaram , S. Valla , B. White and M. Maric
Published/Copyright: April 6, 2013
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Abstract

Telechelic poly(ethylene-ran-butylene) initiator terminated with [tert-butyl[1-(diethoxyphosphoryl)-2,2-dimethylpropyl]amino] nitroxide groups (PEB-(SG1)2) was used to initiate the controlled radical copolymerization of maleic anhydride (MA) and styrene (ST). The ST/MA copolymerizations were performed in 1,4-dioxane at 110°C and resulted in PEB-b-P(ST-ran-MA)2 triblock copolymers with relatively narrow molecular weight distributions (M¯m/M¯n1.5). Gel permeation chromatography (GPC) indicated that the initiator used was ≈93% efficient. The resulting copolymers were then blended as 20 wt.% dispersions in nylon 6 (PA6) at 230°C. With as little as 10 mol.% of MA in the feed to make the PEB-b-P(ST-ran-MA)2, blends were deemed dynamically compatibilized based on the reduced particle size. All of the PEB-b-P(ST-ran-MA)2/PA6 blends resulted in a minor phase particle size D¯vs=0.1 μm while the PEB-b-P(ST)/PA6 blend had D¯vs=1.15 μm (i.e. no MA in the copolymer). Tensile testing revealed yield stresses and strains decreased steadily from pure PA6 to non-reactive PEB-b-P(ST)2/PA6 to PEB-b-P(ST-ran-MA)2/PA6. However, no difference in tensile properties was observed between PEB-b-P(ST-ran-MA)2/PA6 samples made from PEB-b-P(ST-ran-MA)2 copolymer of varying MA content.


Mail address: Milan Maric, Department of Chemical Engineering, McGill University, Montreal, Canada. E-mail:

Dedicated to Prof. Chris Macosko on the occasion of his 65th birthday and presented at the PPS-26 meeting at Banff, AB, Canada, July 4–8, 2010


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Received: 2010-09-24
Accepted: 2010-12-19
Published Online: 2013-04-06
Published in Print: 2011-05-01

© 2011, Carl Hanser Verlag, Munich

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