Experimental study demonstrates coupled plastic upcycling and biomass upgrading via catalyst-driven hydrogen transfer, highlighting a sustainable closed-loop strategy for synthetic refineries.
Waste plastics and biomass represent abundant renewable carbon resources, yet both remain underutilized due to inefficient recycling and valorization strategies. Here, we present a stoichiometrically self-sufficient hydrogen-transfer platform that directly integrates the valorization of oxygenated plastics with the reductive upgrading of biomass derivatives without external hydrogen or reductants. A bifunctional RuPd catalyst supported on rutile mediates selective hydrogen transfer from plastics, such as polyethylene terephthalate (PET), polylactic acid (PLA), and polyoxymethylene (POM), to biomass-derived substrates such as levulinic acid (LA) and guaiacol. Under mild aqueous conditions, the system delivers γ-valerolactone (86%) and terephthalic acid (95%) with high selectivity, a diverse substrate scope, and robust compatibility with real waste streams. Life cycle assessment across multiple functional units demonstrates consistent environmental benefits over conventional routes, including 21–41% lower greenhouse-gas emissions together with reduced resource scarcity and ecosystem-quality impacts. This self-sufficient hydrogen-transfer strategy establishes a modular synthesis platform that unifies plastic upcycling, hydrogen generation, and biomass valorization within a single catalytic system, providing a blueprint for advanced synthetic refineries powered by the complementary reactivity of waste-derived feedstocks.
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Zhang et al. (2026) studied this question.
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