Transfer Hydrogenation with Waste‐Derived Aqueous Solutions of Formic Acid Catalysed by the SulfoShvo Catalyst

The OxFA process provides aqueous formic acid (FA) solutions of around 53 wt% directly from biomass-derived byproducts such as glycerol. The direct utilisation of this diluted FA stream in transfer hydrogenation reactions without neutralisation or buffering is demonstrated, enabled by the highly hydrophilic, acid-stable sulfoShvo catalyst operating at pH 1. Using levulinic acid (LA) as a model substrate, optimisation in pressure autoclaves identified 130 °C and catalyst loadings as low as 0.2 mol% as effective reaction conditions. Even under these harsh acidic conditions, the catalyst displays remarkable performance: at 100 °C, long-term stability is achieved with a turnover number (TON) of 3680, while operation at 130 °C allows efficient hydrogenation but reveals gradual deactivation at very low loadings (0.025 mol%). Beyond LA, a range of water-soluble carbonyl and olefinic substrates is successfully hydrogenated, highlighting the broad applicability of this sustainable approach. Overall, this study establishes the OxFA/sulfoShvo system as a robust and atom-economical strategy for the direct use of biomass-derived FA solutions in catalytic hydrogenation.

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Publication Details

Journal
ChemSusChem
Published
2025-10-27
DOI
https://doi.org/10.1002/cssc.202501832
Primary Topic
Catalysis for Biomass Conversion
Type
article
Field-Weighted Citation Impact
0.00

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article

Transfer Hydrogenation with Waste‐Derived Aqueous Solutions of Formic Acid Catalysed by the SulfoShvo Catalyst

Jakob Albert, Thomas Seidensticker, Justus Diekamp, Milan Danilo Kulaš
ChemSusChem
Catalysis for Biomass Conversion
article

Transfer Hydrogenation with Waste‐Derived Aqueous Solutions of Formic Acid Catalysed by the SulfoShvo Catalyst

Jakob Albert, Thomas Seidensticker, Justus Diekamp, Milan Danilo Kulaš
article en

Abstract

The OxFA process provides aqueous formic acid (FA) solutions of around 53 wt% directly from biomass-derived byproducts such as glycerol. The direct utilisation of this diluted FA stream in transfer hydrogenation reactions without neutralisation or buffering is demonstrated, enabled by the highly hydrophilic, acid-stable sulfoShvo catalyst operating at pH 1. Using levulinic acid (LA) as a model substrate, optimisation in pressure autoclaves identified 130 °C and catalyst loadings as low as 0.2 mol% as effective reaction conditions. Even under these harsh acidic conditions, the catalyst displays remarkable performance: at 100 °C, long-term stability is achieved with a turnover number (TON) of 3680, while operation at 130 °C allows efficient hydrogenation but reveals gradual deactivation at very low loadings (0.025 mol%). Beyond LA, a range of water-soluble carbonyl and olefinic substrates is successfully hydrogenated, highlighting the broad applicability of this sustainable approach. Overall, this study establishes the OxFA/sulfoShvo system as a robust and atom-economical strategy for the direct use of biomass-derived FA solutions in catalytic hydrogenation.

ChemSusChemVol. 18(24)
Universität Hamburg (DE), TU Dortmund University (DE), Hamburg University of Technology (DE)
Bundesministerium für Ernährung und Landwirtschaft
Openalex Percentile: Top 70%
Catalysis for Biomass Conversion
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Transfer Hydrogenation with Waste‐Derived Aqueous Solutions of Formic Acid Catalysed by the SulfoShvo Catalyst — Jakob Albert, Thomas Seidensticker, et al. · ChemSusChem (2025) | TGRS Research Map | TGRS