Aqueous phase hydrogenolysis of glycerol with in situ generated hydrogen over Ni/Al3Fe1 catalyst: effect of the calcination temperature
Resumen: The present work studied the influence of the calcination temperature on the aqueous phase hydrogenolysis of glycerol with in situ generated hydrogen over a Ni/Al3Fe1 catalyst. The Ni/Al3Fe1 catalyst was synthesized by the co-precipitation method at 28 mol% of Ni (Ni/(Ni + Al + Fe)) and a molar ratio of Al/Fe of 3/1. The prepared catalyst was calcined at different temperatures (500–750 °C). The obtained samples were tested for the aqueous phase hydrogenolysis (APH) of glycerol and characterized by several analytical techniques (ICP-OES, H2-TPR, XRD, N2-physisorption, NH3-TPD, STEM, FESEM, and TGA). The catalyst calcined at 625 °C was selected as the best sample due to its high acidity, metal dispersion, and catalytic activity; 1,2-propanediol was the highest carbon selectivity product. In addition, it experienced lower metal leaching than the catalyst calcined at 500 °C
Idioma: Inglés
DOI: 10.1039/d2ra07929a
Año: 2023
Publicado en: RSC Advances 13, 8 (2023), 5483-5495
ISSN: 2046-2069

Factor impacto JCR: 3.9 (2023)
Categ. JCR: CHEMISTRY, MULTIDISCIPLINARY rank: 80 / 231 = 0.346 (2023) - Q2 - T2
Factor impacto CITESCORE: 7.5 - Chemistry (all) (Q1) - Chemical Engineering (all) (Q1)

Factor impacto SCIMAGO: 0.715 - Chemical Engineering (miscellaneous) (Q1) - Chemistry (miscellaneous) (Q2)

Financiación: info:eu-repo/grantAgreement/ES/AEI-FEDER/CTQ2017-86893-R
Financiación: info:eu-repo/grantAgreement/ES/DGA-FEDER/T22-20R
Financiación: info:eu-repo/grantAgreement/ES/MCINN/PID2020-114985RB-I00
Tipo y forma: Article (Published version)
Área (Departamento): Área Ingeniería Química (Dpto. Ing.Quím.Tecnol.Med.Amb.)
Área (Departamento): Área Tecnologi. Medio Ambiente (Dpto. Ing.Quím.Tecnol.Med.Amb.)


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Este artículo se encuentra en las siguientes colecciones:
Articles > Artículos por área > Tecnologías del Medio Ambiente
Articles > Artículos por área > Ingeniería Química



 Record created 2023-04-20, last modified 2024-11-25


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