Rare-Earth MetalModified Co-Based Catalysts for HighlySelective Hydrogenation of Furfural to 1,5-Pentanediol

The ability to effectively control furan ring opening is the key to transforming furfural into 1,5-pentanediol. Herein, a series of Co-based catalysts modified with rare-earth metals (Y, Pr, La, and Ce) were synthesized. It was found that Y-modified Co-based catalyst with a Co/Y molar ratio of 3.5/0.5 exhibited the highest selectivity for 1,5-pentanediol (53.7%) at 150 °C and 4 MPa H<sub>2</sub> in isopropanol (time = 5 h). Coordination between Co and Y in the catalyst resulted in more CoO<sub><i>x</i></sub> and oxygen vacancies, which are vital factors for cleaving the C–O bond of the furan ring. In addition, highly dispersed small-sized Co<sup>0</sup> particles on the catalyst surface could boost the dissociation of H<sub>2</sub> molecules, which attacked the carbonyl group in the furan ring of furfural to afford 1,5-pentanediol. Density functional theory calculations revealed that the presence of CoO<sub><i>x</i></sub>/Y<sub>2</sub>O<sub>3</sub> oxide interfaces promoted adsorption of furfural (especially via the furan ring) and hydrogenolysis during the hydrogenation process. Modifying a Co-based catalyst with rare-earth metals offers a novel approach for producing 1,5-pentanediol from furfural.

Publication Details

Journal
Figshare
Published
2025-03-26
DOI
https://doi.org/10.1021/acs.iecr.4c04382.s001
Primary Topic
Catalysis for Biomass Conversion
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article
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article

Rare-Earth MetalModified Co-Based Catalysts for HighlySelective Hydrogenation of Furfural to 1,5-Pentanediol

Figshare
Catalysis for Biomass Conversion
article

Rare-Earth MetalModified Co-Based Catalysts for HighlySelective Hydrogenation of Furfural to 1,5-Pentanediol

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Abstract

The ability to effectively control furan ring opening is the key to transforming furfural into 1,5-pentanediol. Herein, a series of Co-based catalysts modified with rare-earth metals (Y, Pr, La, and Ce) were synthesized. It was found that Y-modified Co-based catalyst with a Co/Y molar ratio of 3.5/0.5 exhibited the highest selectivity for 1,5-pentanediol (53.7%) at 150 °C and 4 MPa H<sub>2</sub> in isopropanol (time = 5 h). Coordination between Co and Y in the catalyst resulted in more CoO<sub><i>x</i></sub> and oxygen vacancies, which are vital factors for cleaving the C–O bond of the furan ring. In addition, highly dispersed small-sized Co<sup>0</sup> particles on the catalyst surface could boost the dissociation of H<sub>2</sub> molecules, which attacked the carbonyl group in the furan ring of furfural to afford 1,5-pentanediol. Density functional theory calculations revealed that the presence of CoO<sub><i>x</i></sub>/Y<sub>2</sub>O<sub>3</sub> oxide interfaces promoted adsorption of furfural (especially via the furan ring) and hydrogenolysis during the hydrogenation process. Modifying a Co-based catalyst with rare-earth metals offers a novel approach for producing 1,5-pentanediol from furfural.

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Catalysis for Biomass Conversion
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Rare-Earth MetalModified Co-Based Catalysts for HighlySelective Hydrogenation of Furfural to 1,5-Pentanediol · Figshare (2025) | TGRS Research Map | TGRS