BackgroundRecently the plastic pollution and CO2 emission have both become critical issues to be addressed for the sake of a sustainable and carbon-neutral society. To cope with these imminent issues, it is imperative to develop new processes to recycle and reutilize the waste plastics and CO2 produced by anthropogenic activities. MethodsIn this study, the chemical recycling of poly(ethylene terephthalate) (PET) was conducted via a one-pot process, in which PET was degraded into dimethyl terephthalate (DMT) and ethylene glycol (EG) by methanol (MeOH) that was in-situ produced by CO2 hydrogenation over the Cu/ZnO catalyst. The effect of alcohol addition on the one-pot PET methanolysis was investigated in an attempt to enhance the MeOH and DMT yields. Significant findingsOur results reveal that the added isopropanol (i-PrOH) could act as a catalytic solvent to boost the PET degradation (from 31.9% to 63.1% PET conversion) with a high DMT selectivity (92.7%) from the CO2-H2-PET system. Such high DMT selectivity is attributed to the limited PET alcoholysis and DMT transesterification ability of i-PrOH. These findings demonstrate that the one-pot PET methanolysis enabled by i-PrOH-assisted CO2 hydrogenation is a promising approach to valorize waste PET and CO2 simultaneously with a high efficiency.
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