We report here the production of higher-order oligomers from the glycolysis of poly(ethylene terephthalate) (PET) by using microwave irradiation in a controlled fashion, instead of its fully glycolyzed product, bis(2-hydroxyethyl)terephthalate (BHET). We show that different catalysts can generate either BHET as the ultimate glycolysis product or higher oligomers of PET under microwave irradiation. Depolymerization of waste PET with an average degree of polymerization (DP) of 417 from water bottles was performed in the presence of 0.25 wt % antimony(III) oxide (Sb2O3) as the catalyst at 240 °C and 400 W microwave power, resulting in an oligomer yield of 96.7% with an average DP of 37. Under these conditions, the conversion of PET to oligomers reached 100% in only 5 min at 240 °C (with a 10 min ramping time) and with a ethylene glycol to PET weight ratio of 2.5. In comparison, under the same reaction conditions, 0.04 wt % of zinc acetate (Zn(OAc)2), a well-known catalyst for PET glycolysis, produces only the BHET monomer in 96.3% yield. Our results demonstrated that by using Sb2O3, the same catalyst that is used extensively for PET synthesis from BHET, under microwave irradiation, the PET glycolysis can be controlled to produce higher PET oligomers as an alternative for a complete chemical depolymerization to the BHET monomer. These oligomers are more suitable for being used as additives for many applications and to produce high-quality second-generation products, including regenerated PET.
© 2023 The Authors. Published by American Chemical Society.