Synergy between Cu and Lewis Acidic Sites in Cu/Zn-FeO<sub><i>x</i></sub> Catalysts for the Selective Conversion of Poly(ethylene terephthalate) Waste to <i>p</i>-Xylene and Ethylene Glycol
Yuewen Shao, Linghui Kong, Mengjiao Fan, Kai Sun, Guoming Gao, Chao Li, Lijun Zhang, Shu Zhang, Yi Wang, Xun Hu
Abstract
Poly(ethylene terephthalate) (PET)-derived plastics are an important fraction of plastic waste. Selective hydrogenolysis of PET to p -xylene (xylene) and ethylene glycol (EG) could partially recover its value as a chemical feedstock. Herein, Cu/Zn-FeO x catalysts were prepared for the conversion of PET to xylene and EG in 1,4-dioxane at 180–200 °C. The results showed that Zn in Cu/Zn-FeO x created more Lewis acidic sites and enhanced the dispersion of metallic Cu species by developing a porous structure and promoting the reduction of CuO. Cu 2.0 /Zn 1.0 -FeO x was much more active than Cu/FeO x for the conversion of PET to xylene at 180 °C (yield: 93.7% vs 40.7%) but also for further hydrogenolysis of EG, diminishing EG in products. Cu 1.0 /Zn 2.0 -FeO x with a lower availability of Cu sites could also achieve a xylene yield of 98.6% and retain more EG (yield: 53.3%). A kinetic study showed that hydrogenolysis of intermediates like p -tolylmethanol but not hydrogenation was the rate-determining step. The lower activation energy for hydrogenolysis over Cu 2.0 /Zn 1.0 -FeO x than over Cu/FeO x (57.8 vs 65.8 kJ·mol –1 ) rendered the higher turnover frequency for xylene formation. In situ IR characterization showed that Lewis acidic sites induced by Zn addition were important for the adsorption/activation of O-containing functionalities (i.e., C–OH) of the reaction intermediates and consequently further hydrogenolysis.