Catalytic upcycling of polyethylene terephthalate (PET) into high-value oxygenated products is a fascinating process, yet it remains challenging. Here, we present a one-step tandem strategy to realize the thermal catalytic oxidation upcycling of PET to terephthalic acid (TPA) and high-value glycolic acid (GA) instead of ethylene glycol (EG). By using the Au/NiO with rich oxygen vacancies as catalyst, we successfully accelerate the hydrolysis of PET, accompanied by obtaining 99% TPA yield and 87.6% GA yield. The results reveal that the oxygen vacancies in NiO (NiO-O) support tend to adsorb hydrolysis product TPA, preferentially ensuring the strong adsorption of EG at the Au-NiO interface. Moreover, during the EG oxidation process, the Au-NiO interface, composed of two types of structures, quasi "AuNi alloy" and NiO-O, simultaneously promote the C-H bond activation, where Ni in "AuNi alloy" exhibits an oxytropism effect to anchor the C = O bond of the intermediate, while the residual O in NiO-O pillages the H in the C-H bond. Such Au/NiO catalyst is further extended to promote the thermal catalytic oxidation upcycling of other polyethylene glycol esters to GA with excellent catalytic performance.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11685807 | PMC |
| http://dx.doi.org/10.1038/s41467-024-54822-w | DOI Listing |
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