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Ni − Promoted Cu/ZSM-5 for selective hydrodeoxygenation of furfural to produce 2 − Methylfuran
•Ni − Cu/ZSM − 5 prepared by impregnation is used for HDO of furfural to 2 − methylfuran.•Ni − Cu bimetallic sites favor tilted adsorption orientation of furfural.•Ni addition in Cu promote adsorption of furfural and H2 thus accelerate conversion.•Acid sites of zeolite facilitates scission of C − O...
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Published in: | Fuel (Guildford) 2023-12, Vol.353, p.129233, Article 129233 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •Ni − Cu/ZSM − 5 prepared by impregnation is used for HDO of furfural to 2 − methylfuran.•Ni − Cu bimetallic sites favor tilted adsorption orientation of furfural.•Ni addition in Cu promote adsorption of furfural and H2 thus accelerate conversion.•Acid sites of zeolite facilitates scission of C − O in intermediate furfuryl alcohol.
Catalytic hydrodeoxygenation (HDO) of furfural (FUR) to produce 2 − methylfuran (2 − MeF) is a green way to produce hydrocarbons with fuel − like properties. In this work, bimetallic Ni − Cu alloys supported on ZSM − 5 zeolite catalysts were prepared by wetness impregnation and used for HDO of FUR to produce 2 − MeF. Cu/ZSM − 5 catalyst favoured the adsorption of CO bonding in FUR through a tilted adsorption orientation, avoiding the saturation of furan ring. Moderate addition of Ni in Cu/ZSM-5 accelerated the conversion rate with enhanced adsorption of the FUR and H2, leading to high selectivity of 2 − MeF in the product through sequenced hydrogenation and deoxygenation procedures. Moreover, zeolite surface acid benefited the scission of CO bonding in the intermediate furfuryl alcohol (FOL), further promoting the yield of 2 − MeF. The optimized 2Ni − 6Cu/CZ catalyst (with 2 wt% Ni and 6 wt% Cu on ZSM − 5) gave 2 − MeF yield of 78.8 wt% at 220 °C after 30 min reaction. With further increased Ni concentrations, the hydrogenation of furan ring was accelerated with tetrahydrofurfuryl alcohol (THFOL) as the main product. |
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ISSN: | 0016-2361 1873-7153 |
DOI: | 10.1016/j.fuel.2023.129233 |