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- 2011 Annual Meeting
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- Process and Properties In Polymers
- (550c) Flow Accelerates the Reaction Kinetics of Multiphase Polymer Systems
In this paper, a reactive bilayer system was created to explore this issue (Song et al. AIChE J. 2011). In an effort to study the reaction between polyethylene (PE) and thermoplastic polyurethane (TPU), maleic anhydride (MA), hydroxyl (OH) and secondary amine (NHR) functionalized PEs were synthesized via reactive extrusion and blended into non-modified PE. We bonded these PEs to TPU via lamination and coextrusion. In order to compare reaction rates of the two processes we determined the interfacial copolymer density Σ considering both advection and interfacial area generation. We found that the reaction rate in coextrusion was much faster in comparison with lamination at the same temperature. This difference was attributed to the extensional and compressive flow in coextrusion overcoming the diffusion barrier at the interface and forcing reactive species to penetrate into interface. The effects of functional group reactivity and processing variables on adhesion were correlated with interfacial copolymer coverage. Amine functionalized PE showed dramatic adhesion improvement even at 1 wt%. We also determined that flow accelerates the reaction between polyamide 6 and maleic anhydride high density polyethylene. New die design is investigated to isolate the effect of extensional and compressive flow.