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Rubber‐based acrylate resins: An alternative for tire recycling and carbon neutral thermoset materials design
Author(s) -
Tran Thi Kieu Nhung,
Colomines Gaël,
Leroy Eric,
Nourry Arnaud,
Pilard JeanFrançois,
Deterre Rémi
Publication year - 2016
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.43548
Subject(s) - trimethylolpropane , natural rubber , materials science , acrylate , polymer chemistry , thermosetting polymer , vulcanization , prepolymer , elastomer , synthetic resin , monomer , composite material , polymer , polyurethane
Rubber is a widely available potential carbon neutral resource, both as native natural rubber state and as vulcanized state in waste tires. Herein, we describe a model synthesis of acrylate telechelic natural rubber (AcTNR) oligomers and the use of such oligomers to prepare novel acrylate resins. AcTNR oligomers are synthesized according to a two steps procedure implying a controlled C = C bond's scission of high‐molecular‐weight natural rubber and a further chain ends functionalization. The molar mass of the resulting AcTNR is found to be 2300 g/mol as determined by 1 H NMR. AcTNR‐based resins are then prepared by mixing AcTNR oligomers with various reactive diluents (RD) such as styrene, 1,4‐butanediol ether, tri(propylene glycol) diacrylate, 1,6‐hexanediol diacrylate, trimethylolpropane triacrylate (AcTNR:RD weight ratio 7:3). These bio‐based resins are afterward cured in the presence of methyl ethyl ketone peroxide as initiator and cobalt octoate as accelerator at 80 °C and postcured at 120 °C. The cured resins offer a wide range of mechanical, thermal, and dynamic‐mechanical performances. This approach could be extended to rubber tire wastes. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133 , 43548.