Unveiling the Catalytic Role of Zeolite P1 in Carbonylation Reaction

Zeolite P1, a significant conversion product of fly ash, is predominantly utilized for the removal of metal ions, adsorption of carbon dioxide, and capture of aromatic compounds. Despite its diverse applications, its role as a catalyst remains underexplored in the scientific community. Traditionally, mordenite (MOR) zeolites are considered typical dimethyl ether (DME) carbonylation catalysts, whose Brønsted acid sites located on the 8-membered rings (8-MR) are the key active sites for this reaction. This conventional approach underscores the importance of specific zeolite structures in facilitating catalytic processes. H–P1 zeolite was synthesized through a template-free approach in this paper. When applied to DME carbonylation, this zeolite exhibited an impressive selectivity of up to 93% for methyl acetate (MA), suggesting its potential as a highly effective catalyst. This promising outcome hints at a new frontier for the application of the P1 zeolite, potentially revolutionizing its role in catalysis and expanding its utility beyond traditional adsorption processes. The findings suggest that the P1 zeolite could be a versatile material in the realm of catalytic chemistry, offering new pathways and methodologies for various chemical reactions

Alcohol Solvent Assisted Synthesis of Metallic and Metal Oxide Catalysts: As-Prepared Cu/ZnO/Al₂O₃ Catalysts for Low-Temperature Methanol Synthesis with an Ultrahigh Yield

Metallic (Cu/ZnO/Al2O3) and metal oxide (Fe2O3, Co3O4, NiO) catalysts are prepared by a facile alcohol solvent assisted method without additional aging and washing steps. In contrast to the conventional solid-state method using an oxalic acid/M2+ (M = metal cation) molar ratio as high as 4/1, this method is easily operated at room temperature, atmospheric pressure, and an oxalic acid/M2+ molar ratio of only 1.06/1, which prevents the release of lots of flammable gases from the decomposition of excessive oxalic acid. The effect of alcohol solvent types on the physicochemical properties of Cu/ZnO/Al2O3 catalysts and catalytic performance for low-temperature methanol synthesis is systemically studied. Using 1-propanol as solvent, the catalyst realizes an ultrahigh methanol yield of 1782.5 g/kgcat·h–1 at 220 °C and 5.0 MPa, much higher than most reported Cu-based catalysts for conventional high-temperature methanol synthesis. Besides, the Cu/ZnO/Al2O3 catalyst prepared by the alcohol solvent assisted method displayed much higher catalytic activity compared to other catalysts synthesized by conventional methods such as co-precipitation, impregnation, sol–gel, solid-state, and urea hydrolysis. Such good catalytic activity was due to the higher Cu0 surface area, smaller Cu crystallite size, greater surface basicity, and stronger H2 adsorption ability. This work provides not only a hopeful strategy for the large-scale fabrication of metallic and metal oxide catalysts but also a self-catalysis reaction pathway to achieve low-temperature methanol synthesis from CO and CO2 hydrogenation