Terephthalic Acid Copolyesters Containing Tetramethylcyclobutanediol for High-Performance Plastics |
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Authors: | Dr. Samarthya Bhagia Dr. Kamlesh Bornani Dr. Soydan Ozcan Dr. Arthur J. Ragauskas |
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Affiliation: | 1. Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 USA;2. Department of Mechanical Engineering, University of Vermont, Burlington, Vermont 05405 USA;3. Manufacturing Science Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee37831 USA;4. Department of Chemical and Biomolecular Engineering, University of Tennessee, Knoxville, Tennessee 37996 USA |
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Abstract: | There is a need for high-performance applications for terephthalic acid (TPA) polyesters with high heat resistance, impact toughness, and optical clarity. Bisphenol A (BPA) based polycarbonates and polyarylates have such properties, but BPA is an endocrine disruptor. Therefore, new TPA polyesters that are less hazardous to health and the environment are becoming popular. Tetramethylcyclobutanediol (TMCD) is a difunctional monomer that can be polymerized with TPA and other diols to yield copolyesters with superior properties to conventional TPA polyesters. It has a cyclobutyl ring that makes it more rigid than cyclohexanedimethanol (CHDM) and EG. Thus, TMCD containing TPA copolyesters can have high heat resistance and impact strength. TPA can be made from abundantly available upcycled polyethylene terephthalate (PET). Therefore, this review discusses the synthesis of monomers and copolyesters, the impact of diol composition on material properties, molecular weight, effects of photodegradation, health safety, and substitution of cyclobutane diols for future polyesters. |
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Keywords: | polyester copolyesters plastic recycling terephthalic acid tetramethylcyclobutanediol ethylene glycol cyclohexanedimethanol |
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