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Precapture of CO(2) and Hydrogenation into Methanol on Heterogenized Ruthenium and Amine‐Rich Catalytic Systems

A heterogenized alternative to the homogeneous precapture of CO(2) with amines and subsequent hydrogenation to MeOH was developed using aminated silica and a Ru‐MACHO(TM) catalyst. Commercial mesoporous silica was modified with three different amino‐silane monomers and used as support for the Ru cat...

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Detalles Bibliográficos
Autores principales: Szego, Anthony E., Church, Tamara L., Bacsik, Zoltán, Jaworski, Aleksander, Ullah, Latif, Hedin, Niklas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233216/
https://www.ncbi.nlm.nih.gov/pubmed/37259697
http://dx.doi.org/10.1002/open.202300060
Descripción
Sumario:A heterogenized alternative to the homogeneous precapture of CO(2) with amines and subsequent hydrogenation to MeOH was developed using aminated silica and a Ru‐MACHO(TM) catalyst. Commercial mesoporous silica was modified with three different amino‐silane monomers and used as support for the Ru catalyst. These composites were studied by TEM and solid‐state NMR spectroscopy before and after the catalytic reaction. These catalytic reactions were conducted at 155 °C at a H(2) and CO(2) pressures of 75 and 2 bar, respectively, with the heterogeneous system (gas‐solid) being probed with gas‐phase infrared spectroscopy used to quantify the resulting products. High turnover number (TON) values were observed for the samples aminated with secondary amines.