Facile In Situ Synthesis of Supported Gold Catalysts on Ti3AlC2-Based Nanofibers for Selective Oxidation of Biomass-Derived HMF and Aromatic Alcohols
Supported metal catalysts play a significant role in the selective organic synthesis and valorization of bio-derived platform molecules, and the development of catalyst preparation method is an important research topic. The facile in situ reduction synthesis strategy was investigated to prepare gold catalysts on Ti3AlC2-derived nanofibrous materials, using “as-produced H2” during hydrothermal synthesis as a reductive agent. The results of catalyst characterizations revealed that the metallic Au NPs (gold nanoparticles) were loaded with high efficiency. The new series of Aupre/Ti3AlxC2Ty catalysts as prepared by the in situ reduction method generally exhibited higher conversions in the selective oxidation of biomass-derived HMF (5-hydroxymethylfurfural) and aromatic alcohols, outperforming the traditional series of Audp/Ti3AlxC2Ty catalysts as made by the deposition–precipitation method. The HMF conversion was 96.9% over 2%Aupre/Ti3AlxC2Ty and was 76.9% over 2%Audp/Ti3AlxC2Ty. The HMFCA (5-hydroxymethyl-2-furan carboxylic acid) selectivity over these two catalysts was almost identical, whereas it was 96.3% over 1%Aupre/Ti3AlxC2Ty and 84.3% over 1%Audp/Ti3AlxC2Ty. The catalyst reusability tests proved that the typical catalyst Aupre/Ti3AlxC2Ty maintained reaction rates and product selectivity in at least three cycles, whereas the reusability of Audp/Ti3AlxC2Ty catalyst was relatively weaker in both reactions. Finally, the plausible catalytic mechanism was discussed according to peer studies and the research results.
Authors
- Jun Yan (ORCID: https://orcid.org/0000-0002-2840-9348)
- Jun Chen (ORCID: https://orcid.org/0000-0002-8540-5570)
- Xingguang Zhang (ORCID: https://orcid.org/0000-0002-8472-6217)
- Yicheng Sun
Institutions
- University of Shanghai for Science and Technology (CN)
- Nanjing Forestry University (CN)
Publication Details
- Journal
- Materials
- Published
- 2026-09-30
- DOI
- https://doi.org/10.3390/ma19194179
- Primary Topic
- MXene and MAX Phase Materials
- Type
- article
- Field-Weighted Citation Impact
- 0.00