Influence of Ca/P ratio on the catalytic performance of Ni/hydroxyapatite samples in dry reforming of methane

A series of Ni/hydroxyapatite samples presenting different Ca/P molar ratios were synthesised to study the influence of the hydroxyapatite support composition on their catalytic properties in the dry reforming of methane. Our results reveal that a preparation starting from a sub-stoichiometric compo...

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Detalles Bibliográficos
Autores: Boukha, Zouhair, Yeste, María Pilar, Cauqui, Miguel Ángel, González Velasco, Juan Ramón
Tipo de recurso: artículo
Fecha de publicación:2019
País:España
Institución:Universidad del País Vasco
Repositorio:Addi. Archivo Digital para la Docencia y la Investigación
OAI Identifier:oai:addi.ehu.eus:10810/71129
Acceso en línea:http://hdl.handle.net/10810/71129
Access Level:acceso abierto
Palabra clave:Acid/base properties
Ca/P molar ratio
Hydroxyapatite
Methane dry reforming
Ni dispersion
Descripción
Sumario:A series of Ni/hydroxyapatite samples presenting different Ca/P molar ratios were synthesised to study the influence of the hydroxyapatite support composition on their catalytic properties in the dry reforming of methane. Our results reveal that a preparation starting from a sub-stoichiometric composition (Ca/P < 1.67)followed by the impregnation of Ni results in suitable properties which give the highest catalytic performance compared with stoichiometric (Ca/P = 1.67)and over-stoichiometric (Ca/P = 1.73)compositions, respectively. The characterisation of the investigated Ni/HAP materials shows that their texture, surface chemistry (acid/base)and the Ni species distribution are mainly derived from the structural properties of the used support. The activity of the Ni/HAP samples in DRM shows that their performances follow this trend: Ni/HAP-D2 (Ca/P = 1.62)> Ni/HAP-D1 (1.57)> Ni/HAP-S (1.67)> Ni/HAP-E (1.73). The superiority of the sample with a Ca/P molar ratio of 1.62 was explained by a suitable surface chemistry consisting of an abundance of strong acid sites and basic sites. While the former act as anchoring sites for Ni species the latter serve as CO2 chemisorption sites producing intermediate species which in turn react with deposited carbon to form CO. This distribution together with its improved textural properties lead to the deposition of highly dispersed, efficient and coke resistant Ni species.