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Greener and facile synthesis of Cu/ZnO catalysts for CO(2) hydrogenation to methanol by urea hydrolysis of acetates

Cu/ZnO-based catalysts for methanol synthesis by CO(x) hydrogenation are widely prepared via co-precipitation of sodium carbonates and nitrate salts, which eventually produces a large amount of wastewater from the washing step to remove sodium (Na(+)) and/or nitrate (NO(3)(−)) residues. The step is...

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Detalles Bibliográficos
Autores principales: Phongprueksathat, Nat, Bansode, Atul, Toyao, Takashi, Urakawa, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697775/
https://www.ncbi.nlm.nih.gov/pubmed/35424011
http://dx.doi.org/10.1039/d1ra02103f
Descripción
Sumario:Cu/ZnO-based catalysts for methanol synthesis by CO(x) hydrogenation are widely prepared via co-precipitation of sodium carbonates and nitrate salts, which eventually produces a large amount of wastewater from the washing step to remove sodium (Na(+)) and/or nitrate (NO(3)(−)) residues. The step is inevitable since the remaining Na(+) acts as a catalyst poison whereas leftover NO(3)(−) induces metal agglomeration during the calcination. In this study, sodium- and nitrate-free hydroxy-carbonate precursors were prepared via urea hydrolysis co-precipitation of acetate salt and compared with the case using nitrate salts. The Cu/ZnO catalysts derived from calcination of the washed and unwashed precursors show catalytic performance comparable to the commercial Cu/ZnO/Al(2)O(3) catalyst in CO(2) hydrogenation at 240–280 °C and 331 bar. By the combination of urea hydrolysis and the nitrate-free precipitants, the catalyst preparation is simpler with fewer steps, even without the need for a washing step and pH control, rendering the synthesis more sustainable.