Modulating activity and selectivity of aqueous phase furfuryl alcohol hydrogenation by tuning supported Pt on W-Zr Mixed oxides

This work investigated a mixed W x Zr y oxide supported-platinum catalyst for the selective synthesis of cyclopentanone (CPO) from furfuryl alcohol (FOL). The tuning effect of different W and Zr molar ratio with varying Pt loadings at various operating temperatures and P H 2 were explored under aqueous phase conditions in a flow-through configuration. Different WO x domain and Pt 0 crystallite sizes were obtained as a function of Zr content in the supports. These modulations exhibited distinct selectivities towards the reaction intermediates. Furthermore, water was found to complement as a source of homogeneous catalysis for FOL rearrangement at high temperatures. Minimal hydrogenation intermediates were detected using only W x Zr y supports. While the presence of Pt does enhance hydrogenation activity, it also resulted in reduction of WO x domains necessary for reaction steps beyond FOL rearrangement. This effect was found to be more pronounced with increasing W concentration in the supports. Regardless of the catalyst formulation used, increasing P H 2 resulted in lower hydrogenation activity. Conducting experiments with catalysts at various synthetic steps led to a comprehensive resolution of the reaction mechanism. A two-step metal induced hydrogenation of the intermediate, 4H2CP, was found to be the slowest step in the reaction network to obtain CPO. This bottleneck could only be overcome by slightly increasing Pt content in the catalyst, resulting in ∼ 64 % CPO yield and high selectivity for sample with lowest W content. Long-term operation of the catalytic bed demonstrated stable activity for at least 38 h of continuous operation. • CPO selectivity is tunable as function of W/Zr ratio. • Water dissociation contributes towards FOL rearrangement to 4H2CP. • Hydrogenation of 4H2CP followed by dehydration to CPEN is preferred. • Pt loading influences 4H2CP conversion to CPO by double step hydrogenation. • High stability and CPO productivity is achieved by tuning Pt and W/Zr loading.

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Publication Details

Journal
Applied Catalysis B: Environmental
Published
2025-04-23
DOI
https://doi.org/10.1016/j.apcatb.2025.125400
Citations
5
Primary Topic
Catalysis for Biomass Conversion
Type
article
Field-Weighted Citation Impact
3.37

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article

Modulating activity and selectivity of aqueous phase furfuryl alcohol hydrogenation by tuning supported Pt on W-Zr Mixed oxides

Svilen Plamenov Simeonov, Adarsh Patil, Consolato Rosmini, Fernanda Neira D’Angelo et al.
5 citations
Applied Catalysis B: Environmental
Catalysis for Biomass Conversion
3.37
article

Modulating activity and selectivity of aqueous phase furfuryl alcohol hydrogenation by tuning supported Pt on W-Zr Mixed oxides

Svilen Plamenov Simeonov, Adarsh Patil, Consolato Rosmini, Fernanda Neira D’Angelo, Anish Kumar Kodyingal
article en
5 citations

Abstract

This work investigated a mixed W x Zr y oxide supported-platinum catalyst for the selective synthesis of cyclopentanone (CPO) from furfuryl alcohol (FOL). The tuning effect of different W and Zr molar ratio with varying Pt loadings at various operating temperatures and P H 2 were explored under aqueous phase conditions in a flow-through configuration. Different WO x domain and Pt 0 crystallite sizes were obtained as a function of Zr content in the supports. These modulations exhibited distinct selectivities towards the reaction intermediates. Furthermore, water was found to complement as a source of homogeneous catalysis for FOL rearrangement at high temperatures. Minimal hydrogenation intermediates were detected using only W x Zr y supports. While the presence of Pt does enhance hydrogenation activity, it also resulted in reduction of WO x domains necessary for reaction steps beyond FOL rearrangement. This effect was found to be more pronounced with increasing W concentration in the supports. Regardless of the catalyst formulation used, increasing P H 2 resulted in lower hydrogenation activity. Conducting experiments with catalysts at various synthetic steps led to a comprehensive resolution of the reaction mechanism. A two-step metal induced hydrogenation of the intermediate, 4H2CP, was found to be the slowest step in the reaction network to obtain CPO. This bottleneck could only be overcome by slightly increasing Pt content in the catalyst, resulting in ∼ 64 % CPO yield and high selectivity for sample with lowest W content. Long-term operation of the catalytic bed demonstrated stable activity for at least 38 h of continuous operation. • CPO selectivity is tunable as function of W/Zr ratio. • Water dissociation contributes towards FOL rearrangement to 4H2CP. • Hydrogenation of 4H2CP followed by dehydration to CPEN is preferred. • Pt loading influences 4H2CP conversion to CPO by double step hydrogenation. • High stability and CPO productivity is achieved by tuning Pt and W/Zr loading.

Applied Catalysis B: EnvironmentalVol. 375
University of Lisbon (PT), Bulgarian Academy of Sciences (BG), Institute of Organic Chemistry with Centre of Phytochemistry (BG), Eindhoven University of Technology (NL)
European Commission, Horizon 2020 Framework Programme, European Regional Development Fund
Clean water and sanitation
Openalex Percentile: Top 8%
Catalysis for Biomass Conversion
3.37
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