A1 Refereed original research article in a scientific journal
Synthesis and Characterization Ru–C/SiO2 Aerogel Catalysts for Sugar Hydrogenation Reactions
Authors: Sanz-Moral L., Aho A., Kumar N., Eränen K., Peurla M., Peltonen J., Murzin D., Salmi T.
Publisher: Springer New York LLC
Publication year: 2018
Journal: Catalysis Letters
Journal name in source: Catalysis Letters
Volume: 148
Issue: 11
First page : 3514
Last page: 3523
Number of pages: 10
ISSN: 1011-372X
eISSN: 1572-879X
DOI: https://doi.org/10.1007/s10562-018-2556-4
Web address : https://link.springer.com/article/10.1007/s10562-018-2556-4
Synthesis of materials with combined chemistry and textural properties of carbon and silica aerogels was studied. The synthesized support was modified with ruthenium using evaporation impregnation and deposition–precipitation methods. The ruthenium modification methods were observed to influence the particle size, dispersion, surface area, pore volume and acidity of Ru–C–SiO2 catalysts. Ruthenium particles of 1–2 nm were obtained with a simple impregnation–evaporation method, while deposition precipitations technique gave ruthenium particles ranging from 1 to 8 nm. Small Ru nanoparticles (1–2 nm) were stable even after being exposed at 700 °C or washed with ethanol for regeneration. Furthermore, the catalytic properties of Ru–C–SiO2 catalysts in sugar hydrogenation were also observed to be influenced by the synthesis methods. The catalysts were tested in hydrogenation of sugars with different molecule sizes (i.e. glucose and cellobiose). d-Glucose was more reactive than d-cellobiose when they were studied separately. For the mixture of sugars higher reactivity of both sugars was observed in comparison with neat substrates for the catalyst made by evaporation-impregnation. On the contrary no significant differences between kinetics of the separated sugars and their mixture were observed for the catalyst prepared by deposition–precipitation. The results can be attributed to acidity and a combination of meso and microporosity of the catalysts. The support composite material could also be produced as a monolith, being a promising candidate for future industrial applications.