Carbonylation of dimethyl ether in mordenite using Inelastic Neutron Scattering
[EN] Zeolite mordenite (MOR, Si/Al =10) was used as catalyst for the reaction between CO and dimethyl ether (DME) to give methyl acetate. Since the reaction is catalysed by Bronsted acid sites, Inelastic Neutron Scattering (INS) is an appropriate technique to identify the intermediates. Although the...
| Autores: | , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2024 |
| País: | España |
| Institución: | Universitat Politècnica de València (UPV) |
| Repositorio: | RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia |
| Idioma: | inglés |
| OAI Identifier: | oai:riunet.upv.es:10251/203420 |
| Acceso en línea: | https://riunet.upv.es/handle/10251/203420 |
| Access Level: | acceso abierto |
| Palabra clave: | Carbonylation Dimethyl ether Zeolite Inelastic neutron scattering Mordenite |
| Sumario: | [EN] Zeolite mordenite (MOR, Si/Al =10) was used as catalyst for the reaction between CO and dimethyl ether (DME) to give methyl acetate. Since the reaction is catalysed by Bronsted acid sites, Inelastic Neutron Scattering (INS) is an appropriate technique to identify the intermediates. Although the accepted mechanism goes through an adsorbed methoxy, its characteristic peak at 963 cm-1 was only detected in the reaction MOR + DME, in the absence of CO. When CO is present, the peak at 963 cm-1 is substituted by other peaks that give valuable in-formation of the reaction intermediates, indicating that either methoxy intermediates are not formed or are quickly replaced by the acetyl intermediate, [SiO(COCH3)Al], strongly stabilised in the micropore pockets of mordenite. Upon reaction of MOR + CO + DME, a characteristic peak at 1050 cm-1, although being present in liquid methyl acetate, could not be assigned to adsorbed methyl acetate since it loses intensity as the reaction proceeds (upon heating), and was assigned to a strong interaction between CO and DME adsorbed in one or two Bronsted sites, leading to some intermediate that shares this vibrational feature with methyl acetate in liquid phase. Finally, a peak at 1275 cm-1 in the spectrum of MOR + CO + DME upon heating is assigned to the formation of methyl acetate when the sample is heated, corresponding to C-O stretching of methyl acetate. This is further confirmed by the absence of this peak before heating. Overall, INS technique has allowed an accurate determination and interpretation of peaks involved in the carbonylation of DME in mordenite. |
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