Reusable Nitrogen‐Doped Carbon‐Encapsulated Cobalt Catalyst for Efficient Stepwise Oxidation of Acetal‐Protected 5‐Hydroxy‐Methylfurfural to Furan‐2,5‐Dicarboxylic Acid

We report a ZIF‐67‐derived N‐doped carbon‐encapsulated cobalt catalyst (Co@N‐C) for the efficient, reusable, and noble metal‐free aerobic oxidation of concentrated aqueous 5‐hydroxymethylfurfural (HMF) derivatives in a stepwise fashion to furan‐2,5‐dicarboxylic acid (FDCA). Using acetal‐protected HMF with propane‐1,3‐diol (PD‐HMF) to suppress degradation at high substrate concentrations, Co@N‐C‐800p (Co‐containing ZIF‐67 pyrolyzed at 800 °C) delivers high yields in water while enabling effective PDO recovery. At 20 wt% PD‐HMF, a 96.8% yield of PD‐FFCA (acetal‐protected form of FFCA, 5‐formylfuran‐2‐carboxylic acid) was obtained at 99.2% conversion. Subsequent deprotection afforded FFCA and enabled recovery of propane‐1,3‐diol, after which FFCA was oxidized separately under the same conditions to FDCA in a 93.6% yield. Replacing soluble alkali carbonates with sparingly soluble Ca(OH) 2 provides buffered alkalinity that enhances formyl group oxidation, minimizes by‐products, and limits PDO loss at reduced base loadings. Radical scavenger experiments indicate a mechanism involving oxygen‐derived species that regenerate metallic Co sites via hydride removal. Although partial deactivation occurs through cobalt surface oxidation and CaCO 3 accumulation, full catalytic performance is restored by re‐pyrolysis. Overall, this work establishes Co@N‐C as an efficient, stable, and regenerable non‐noble metal catalyst for aerobic FDCA production at industrially relevant substrate concentrations.

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Journal
ChemSusChem
Published
2026-09-04
DOI
https://doi.org/10.1002/cssc.71023
Primary Topic
Catalysis for Biomass Conversion
Type
article
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article

Reusable Nitrogen‐Doped Carbon‐Encapsulated Cobalt Catalyst for Efficient Stepwise Oxidation of Acetal‐Protected 5‐Hydroxy‐Methylfurfural to Furan‐2,5‐Dicarboxylic Acid

Jan J. Wiesfeld, Kiyotaka Nakajima, Ryota Osuga, Satoshi Suganuma et al.
ChemSusChem
Catalysis for Biomass Conversion
article

Reusable Nitrogen‐Doped Carbon‐Encapsulated Cobalt Catalyst for Efficient Stepwise Oxidation of Acetal‐Protected 5‐Hydroxy‐Methylfurfural to Furan‐2,5‐Dicarboxylic Acid

Jan J. Wiesfeld, Kiyotaka Nakajima, Ryota Osuga, Satoshi Suganuma, Emiel J. M. Hensen
article en

Abstract

We report a ZIF‐67‐derived N‐doped carbon‐encapsulated cobalt catalyst (Co@N‐C) for the efficient, reusable, and noble metal‐free aerobic oxidation of concentrated aqueous 5‐hydroxymethylfurfural (HMF) derivatives in a stepwise fashion to furan‐2,5‐dicarboxylic acid (FDCA). Using acetal‐protected HMF with propane‐1,3‐diol (PD‐HMF) to suppress degradation at high substrate concentrations, Co@N‐C‐800p (Co‐containing ZIF‐67 pyrolyzed at 800 °C) delivers high yields in water while enabling effective PDO recovery. At 20 wt% PD‐HMF, a 96.8% yield of PD‐FFCA (acetal‐protected form of FFCA, 5‐formylfuran‐2‐carboxylic acid) was obtained at 99.2% conversion. Subsequent deprotection afforded FFCA and enabled recovery of propane‐1,3‐diol, after which FFCA was oxidized separately under the same conditions to FDCA in a 93.6% yield. Replacing soluble alkali carbonates with sparingly soluble Ca(OH) 2 provides buffered alkalinity that enhances formyl group oxidation, minimizes by‐products, and limits PDO loss at reduced base loadings. Radical scavenger experiments indicate a mechanism involving oxygen‐derived species that regenerate metallic Co sites via hydride removal. Although partial deactivation occurs through cobalt surface oxidation and CaCO 3 accumulation, full catalytic performance is restored by re‐pyrolysis. Overall, this work establishes Co@N‐C as an efficient, stable, and regenerable non‐noble metal catalyst for aerobic FDCA production at industrially relevant substrate concentrations.

ChemSusChemVol. 19(17)
Tohoku University (JP), Hokkaido University (JP), Eindhoven University of Technology (NL)
Clean water and sanitation
Openalex Percentile: Top 20%
Catalysis for Biomass Conversion
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