Utility of Chemical Upcycling in Transforming Postconsumer PET to PBT-Based Thermoplastic Copolyesters Containing a Renewable Fatty-Acid-Derived Soft Block.

Abstract

Thermoplastic copolyesters (TPCs) are important structural components in countless high performance applications that require excellent thermal stability and outstanding mechanical integrity. Segmented multiblock architectures are often employed for the most demanding applications, in which semicrystalline segments of poly(butylene terephthalate) (PBT) are combined with various low T g soft blocks. These segmented copolymers are nearly always synthesized from pristine feedstocks that are derived from fossil-fuel sources. In this work, we show a straightforward, one-pot synthetic approach to prepare TPCs starting from high-molar mass poly(ethylene terephthalate) recyclate (rPET) combined with a hydrophobic fatty acid dimer diol flexible segment. Transesterification is exploited to create a multiblock architecture. The high molar mass and segment distribution are elucidated by detailed size-exclusion chromatography and proton and carbon nuclear magnetic resonance spectroscopy. It is also shown that rPET can be chemically converted to PBT through a molecular exchange, in which the ethylene glycol is substituted by introducing 1,4-butane diol. A series of copolymers with various compositions was prepared with either PET or PBT segments and the final thermal properties and mechanical performance is compared between the two different constructs. Ultimately, PBT-based TPCs crystallize faster and exhibit a higher modulus over the range of explored compositions, making them ideal for applications that require injection molding. This represents an ideal, sustainable approach to making conventional TPCs, utilizing recyclate and biobased components to produce high performance polymer constructs via an easily accessible upcycling route.