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Ethanol Dehydrogenation over Copper-Silica Catalysts: From Sub-Nanometer Clusters to 15 nm Large Particles

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    0574069 - ÚFM 2024 RIV US eng J - Journal Article
    Pokorný, T. - Vykoukal, V. - Machač, P. - Moravec, Z. - Scotti, N. - Roupcová, Pavla - Karásková, K. - Stýskalík, A.
    Ethanol Dehydrogenation over Copper-Silica Catalysts: From Sub-Nanometer Clusters to 15 nm Large Particles.
    ACS Sustainable Chemistry & Engineering. Roč. 11, č. 30 (2023), s. 10980-10992. ISSN 2168-0485. E-ISSN 2168-0485
    Institutional support: RVO:68081723
    Keywords : ethanol dehydrogenation * copper * nanoparticles * acetaldehyde * sol-gel * dry impregnation
    OECD category: Particles and field physics
    Impact factor: 8.4, year: 2022
    Method of publishing: Open access
    https://pubs.acs.org/doi/10.1021/acssuschemeng.2c06777

    Comparison of four preparation methodsshowed that the simpleand cost-effective dry impregnation provides Cu/SiO2 materialshowing the most stable catalytic behavior in potential renewableacetaldehyde production despite having a broad particle size distribution.

    Non-oxidative ethanoldehydrogenation is a renewable source ofacetaldehyde and hydrogen. The reaction is often catalyzed by supportedcopper catalysts with high selectivity. The activity and long-termstability depend on many factors, including particle size, choiceof support, doping, etc. Herein, we present four different syntheticpathways to prepare Cu/SiO2 catalysts (& SIM,2.5 wt %Cu) with varying copper distribution: hydrolytic sol-gel (sub-nanometerclusters), dry impregnation (A ̅ = 3.4 nm, & sigma,= 0.9 nm and particles up to 32 nm), strong electrostatic adsorption(A ̅ = 3.1 nm, & sigma, = 0.6 nm), and solvothermalhot injection followed by Cu particle deposition (A ̅ = 4.0 nm, & sigma, = 0.8 nm). All materials were characterized byICP-OES, XPS, N-2 physisorption, STEM-EDS, XRD, RFC N2O, and H-2-TPR and tested in ethanol dehydrogenationfrom 185 to 325 & DEG,C. The sample prepared by hydrolytic sol-gelexhibited high Cu dispersion and, accordingly, the highest catalyticactivity. Its acetaldehyde productivity (2.79 g g(-1) h(-1) at 255 & DEG,C) outperforms most of the Cu-basedcatalysts reported in the literature, but it lacks stability and tendsto deactivate over time. On the other hand, the sample prepared bysimple and cost-effective dry impregnation, despite having Cu particlesof various sizes, was still highly active (2.42 g g(-1) h(-1) acetaldehyde at 255 & DEG,C). Importantly,it was the most stable sample out of the studied materials. The characterizationof the spent catalyst confirmed its exceptional properties: it showedthe lowest extent of both coking and particle sintering.
    Permanent Link: https://hdl.handle.net/11104/0344436

     
     
Number of the records: 1  

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