Activation of n-pentane while prolonging HZSM-5 catalyst lifetime during its combined reaction with methanol or dimethyl ether

[EN] This work explores the synergies during combined reactions of n-pentane (nC5) with oxygenates (methanol or dimethyl ether, OX). The experimental runs have been carried out in a packed bed reactor at 500 °C, using a high silica HZSM-5 zeolite-based catalyst with different oxygenate-to-n-pentane...

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Detalles Bibliográficos
Autores: Cordero-Lanzac, Tomás, Aguayo, Andrés T., Castaño, Pedro, Bilbao, Javier, Martínez, Cristina|||0000-0002-4415-084X, Corma Canós, Avelino|||0000-0002-2232-3527
Tipo de recurso: artículo
Fecha de publicación:2022
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:10251/194526
Acceso en línea:https://riunet.upv.es/handle/10251/194526
Access Level:acceso abierto
Palabra clave:Olefins
HZSM-5 zeolite
Catalytic cracking
Dual-cycle mechanism
Deactivation,Coke
Descripción
Sumario:[EN] This work explores the synergies during combined reactions of n-pentane (nC5) with oxygenates (methanol or dimethyl ether, OX). The experimental runs have been carried out in a packed bed reactor at 500 °C, using a high silica HZSM-5 zeolite-based catalyst with different oxygenate-to-n-pentane (OX/nC5) ratios in the feed. A significant enhancement of the n-pentane conversion occurs for low OX/nC5 ratios in the feed (0.1¿0.25), especially when using dimethyl ether (DME). In addition, the presence of n-pentane reduces the rate of catalyst deactivation by coking during the conversion of oxygenates. These results have been explained on the grounds of a mechanistic interaction between the reactants: (1) the fast formation of methoxy and olefin intermediates from oxygenates, particularly from DME, could explain the promotion of n-pentane cracking, by facilitating the activation of the alkane by hydrogen transfer reactions; (2) the attenuation of deactivation during the conversion of oxygenates could be related to a lower extent of the arene cycle in the dual-cycle mechanism (limiting the polymethylbenzene formation). The analyses of used catalysts by means of temperature-programmed oxidation and confocal fluorescence microscopy have pointed out the higher reactivity of DME than that of methanol also for yielding coke structures.