Subcritical CO2–H2O hydrolysis of polyethylene terephthalate as a sustainable chemical recycling platform
The development of an efficient and environmentally sustainable chemical hydrolysis process for recycling waste plastics, based on green chemistry principles, is a key challenge. In this work, we investigated the role of subcritical CO2 on the hydrolysis of polyethylene terephthalate (PET) into tere...
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Published in | Green chemistry : an international journal and green chemistry resource : GC Vol. 26; no. 11; pp. 6436 - 6445 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
2024
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Subjects | |
Online Access | Get full text |
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Summary: | The development of an efficient and environmentally sustainable chemical hydrolysis process for recycling waste plastics, based on green chemistry principles, is a key challenge. In this work, we investigated the role of subcritical CO2 on the hydrolysis of polyethylene terephthalate (PET) into terephthalic acid (TPA) at 180–200 °C for 10–100 min. The addition of CO2 into the reaction mixture led to the in situ formation of carbonic acid that helps to catalyze PET hydrolysis relative to hot compressed H2O (i.e. N2–H2O). The highest TPA yield of 85.0 ± 1.3% was obtained at 200 °C, PET loading of 2.5 g PET in 20 mL H2O for 100 min, and 208 psi of initial CO2 pressure. In addition, the subcritical CO2–H2O system demonstrated high selectivity toward hydrolyzing PET in a mixture with polyethylene (PE) at 200 °C for 100 min, thus providing “molecular sorting” capabilities to the recycling process. The robustness of the process was also demonstrated by the ability to hydrolyze both colored Canada Dry and transparent Pure Life® waste PET bottles into high yields of TPA (>86%) at 200 °C. In addition, subcritical CO2–H2O hydrolysis of colored PET bottles resulted in a white TPA product similar to that generated from transparent PET bottles. Overall, this work shows that, under optimized reaction conditions, subcritical CO2 can provide acid tunability to the reaction medium to favor waste PET hydrolysis for subsequent recycling. |
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Bibliography: | USDOE NREL/JA-2800-89212 National Science Foundation (NSF) AC36-08GO28308; OIA-2119754 USDOE Office of Energy Efficiency and Renewable Energy (EERE), Office of Sustainable Transportation. Bioenergy Technologies Office (BETO) USDOE Office of Energy Efficiency and Renewable Energy (EERE), Energy Efficiency Office. Advanced Manufacturing and Materials Technologies Office (AMMTO) |
ISSN: | 1463-9262 1463-9270 |
DOI: | 10.1039/d3gc04576e |