Efficient dehydrogenation of ethanol to acetaldehyde over silica supported Cu catalyst prepared from microwave-assisted wet-kneading
• Cu@SiO 2 -WK catalyst was prepared from microwave-assisted wet-kneading. • The wet-kneading method render the construction of core–shell structure. • Cu@SiO 2 -WK is active, selective and stable for ethanol dehydrogenation to acetaldehyde. • The core–shell structure in Cu@SiO 2 -WK is important for catalytic stability. Cu-based catalysts are crucial for the dehydrogenation of ethanol (EtOH) to acetaldehyde (AcH); however, their performance decreases at higher temperatures due to the low Tammann temperature of Cu species. In this study, we synthesized silica-supported Cu catalysts using microwave-assisted wet-kneading. Characterizations revealed a typical core–shell structure (Cu@SiO 2 -WK), which demonstrated high activity, excellent selectivity, and superior stability for ethanol dehydrogenation . The Cu@SiO 2 -WK achieved 96.2 % EtOH conversion with 99.9 % selectivity to AcH at 260 °C. After 160 h of reaction, it maintained an EtOH conversion of 90.5 % and AcH selectivity of ∼99.9 %. Following simple calcination, the catalyst’s activity was fully regenerated to 96.1 %. Model catalysts and in situ FT-IR spectra indicate that the core–shell structure significantly enhances the catalyst’s performance in the dehydrogenation of EtOH to AcH.
Authors
- Zerui Su
- Zhi Qiao (ORCID: https://orcid.org/0000-0002-8942-5907)
- Xianmin Mu (ORCID: https://orcid.org/0000-0002-2365-9321)
- Feng‐Shou Xiao (ORCID: https://orcid.org/0000-0001-9744-3067)
- Xiaoyuan Qin
- Lei Wei (ORCID: https://orcid.org/0000-0002-1546-6458)
- Jian Zhang (ORCID: https://orcid.org/0000-0002-6662-2967)
- Ziyuan Qiao
- Yang Li (ORCID: https://orcid.org/0000-0002-8168-5544)
Institutions
- Beijing University of Chemical Technology (CN)
- Zhejiang University (CN)
Publication Details
- Journal
- Chemical Engineering Science
- Published
- 2025-04-11
- DOI
- https://doi.org/10.1016/j.ces.2025.121664
- Citations
- 2
- Primary Topic
- Catalysis for Biomass Conversion
- Type
- article
- Field-Weighted Citation Impact
- 1.35
Funders
- National Natural Science Foundation of China