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Reactive‐extrusion route for the closed‐loop recycling of poly(ethylene terephthalate)
Author(s) -
Kiliaris P.,
Papaspyrides C. D.,
Pfaendner R.
Publication year - 2007
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.25795
Subject(s) - reactive extrusion , crystallinity , materials science , branching (polymer chemistry) , extrusion , pyromellitic dianhydride , extender , polymer , ethylene , melt flow index , chemical engineering , polymer chemistry , rheology , molar mass distribution , polypropylene , catalysis , composite material , organic chemistry , chemistry , copolymer , polyimide , layer (electronics) , polyurethane , engineering
The effectiveness of the reactive extrusion technique was investigated for poly(ethylene terephthalate) to promote the concept of closed‐loop recycling, that is, the reuse of waste material in the initial application. More specifically, a chain‐extender system, consisting of pyromellitic dianhydride, polyol, and a catalyst, was employed, and its efficiency regarding the improvement of the recyclate quality was evaluated. Accordingly, rheological and thermal characterizations were performed and used as criteria of the modification induced in the polymer molecular structure during processing due to the counteracting degradation and chain‐extension reactions. In particular, the molecular weight, related to intrinsic viscosity and melt flow rate measurements, of modified poly(ethylene terephthalate) samples was found to increase with the additive content. Simultaneously, a decrease in the crystallinity was observed, attributed to the branching effect of the chain extender, which restricted the ability of the macromolecules to organize in the crystal structure. Beyond a critical concentration of the additive system, the molecular weight of the treated samples started to decrease again, and this was accompanied by a small increase in the crystallinity. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 1671–1678, 2007