Conversion of Levulinic acid into chemicals: Synthesis of biomass derived levulinate esters over Zr-containing MOFs

Zr-containing metal-organic frameworks (MOFs) formed by either terephthalate (UiO-66) or 2-aminoterephthalate ligancls (UiO-66-NH2) are active and stable catalysts for the acid catalyzed esterification of levulinic acid with EtOH, n-BuOH and long-chain biomass derived alcohols, with activities compa...

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Detalles Bibliográficos
Autores: García Cirujano, Francisco, Corma Canós, Avelino|||0000-0002-2232-3527, Llabrés i Xamena, Francesc Xavier|||0000-0002-4238-5784
Tipo de recurso: artículo
Fecha de publicación:2015
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:10251/71219
Acceso en línea:https://riunet.upv.es/handle/10251/71219
Access Level:acceso abierto
Palabra clave:MOF catalysis
Biomass into chemicals
Levulinic acid esterification
Dual acid-base activation
QUIMICA ORGANICA
Descripción
Sumario:Zr-containing metal-organic frameworks (MOFs) formed by either terephthalate (UiO-66) or 2-aminoterephthalate ligancls (UiO-66-NH2) are active and stable catalysts for the acid catalyzed esterification of levulinic acid with EtOH, n-BuOH and long-chain biomass derived alcohols, with activities comparable (in some cases superior) to other solid acid catalysts previously repotted. The effect of functional group substitution at the ligand benzene ring, alcohol chain length, particle size and contents of defects on the catalytic activity of the MOFs are studied in detail. In UiO-66-NH2, a dual acid-base activation mechanism is proposed, in which levulinic acid is activated on Zr sites and the alcohol at the amino groups of the ligand. Large variations of the catalytic activity from batch to batch suggest that the active sites are located at defect positions associated to ligand deficiency of the solid. Particle size seems to have a minor impact only in UiO-66-NH2, in which diffusion of levulinic acid is somehow hindered due to the amino groups present in the linkers.