催化作用
钌
氢
聚酯纤维
化学
核化学
材料科学
有机化学
作者
Yawen Shi,Shengbo Zhang,Xinyong Diao,Zongyang Ya,Hu Ding,Kaihao Cao,Ruhan Wei,Mei Li,Qingling Liu,Na Ji
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-07-11
卷期号:15 (15): 12640-12651
被引量:19
标识
DOI:10.1021/acscatal.5c00927
摘要
Chemical upcycling of plastic waste into high-value chemicals or fuels could mitigate environmental pollution and create a more sustainable society. Hydrolytic depolymerization is a viable method for polyester recycling but typically requires high temperature to drive this reaction and complete subsequent distillation operations to separate a diol from the aqueous phase. Here, through theoretical screening, we discover a Ruδ+–Ru0 dual-site catalyst can achieve the tandem PET (polyethylene terephthalate) depolymerization and in situ reforming of ethylene glycol (EG) under mild conditions. Mechanism studies reveal that the Ruδ+ site can selectively promote adsorption and C–H bond dissociation, yet C–C bond cleavage takes place on both Ruδ+ and Ru0 sites, which synergistically promotes PET and EG conversion and helps avoid excessive oxidation of intermediates to CO2 or CO. As a result, this catalyst delivers a conversion of 100% toward PET and EG into high-value organic acids, including terephthalic acid, and high-purity H2 with a generation rate of 1.03 m3 kgPET–1 d–1 gCat–1 at 90 °C. Besides, this catalyst is catalytically active toward a wide scope of substrates, including real-world waste PET products, PET-containing mixed plastics, and other polyester plastics. Techno-economic analysis and environmental assessment show that this integration process can significantly increase net profits and reduce carbon emissions.
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