双金属片
催化作用
聚对苯二甲酸乙二醇酯
糖酵解
聚乙烯
化学
化学工程
材料科学
无机化学
有机化学
酶
复合材料
工程类
作者
Phuong Ha,Thao P. Nguyen,Thao P. Nguyen,Trinh Duy Nguyen,Trinh Duy Nguyen,Duong Dinh Pham,Tri T. Phan,Thi H. Ho,Dang Le Tri Nguyen,Tung M. Nguyen,Tung M. Nguyen
标识
DOI:10.1021/acssuschemeng.5c02598
摘要
The overuse of polyethylene terephthalate (PET) plastics has led to severe waste accumulation with a large portion of PET ending up in landfills or being incinerated despite ongoing recycling efforts. Chemical recycling, particularly glycolysis, offers a promising method for transforming PET waste into valuable monomers, such as bis(2-hydroxyethyl) terephthalate (BHET). This study introduces a highly efficient bimetallic Zn–Mn catalyst supported on commercial SiO 2 for PET glycolysis. The synergy between Zn and Mn leads to the formation of a new active site, ZnMn 2 O 4, which significantly improves catalytic activity and BHET selectivity compared with monometallic catalysts. Density functional theory (DFT) calculations show the bimetallic system has a smaller energy gap between the adsorption energies of ethylene glycol and PET, facilitating better interaction with the catalyst. At the optimal Zn/Mn molar ratio of 1:1, the catalyst achieved a space-time yield of 114.86 mol BHET ·mol cat –1 ·h –1, surpassing those of other reported heterogeneous catalysts. The strong Zn–Mn bond reduces metal leaching, contributing to excellent catalyst stability. After five cycles, PET conversion decreased slightly from 92.08% to 88.15%, and BHET yield dropped from 88.29% to 84.97% due to some loss of active sites. Nevertheless, product selectivity remained high (95–96%), aiding in efficient separation and purification.
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