Highly Active Catalytic Ruthenium/TiO2 Nanomaterials for Continuous Production of γ-Valerolactone

Green energy production from renewable sources is an attractive, but challenging topic to face the likely energy crisis scenario in the future. In the current work, a series of versatile Ru/TiO2 catalysts were simply synthesized and employed in continuous-flow catalytic transfer hydrogenation of industrially derived methyl levulinate biowaste (from Avantium Chemicals B.V.) to form γ-valerolactone. Different analytical techniques were applied in the characterization of the as-synthesized catalysts, including XRD, SEM, energy-dispersion X-ray spectroscopy, TEM, and X-ray photoelectron spectroscopy. The effects of various reaction conditions (e.g., temperature, concentration, and flow rate) were investigated. Results suggested that optimum dispersion and distribution of Ru on the TiO2 surface could efficiently promote the production of γ-valerolactone; the 5 % Ru/TiO2 catalyst provided excellent catalytic performance and stability compared with commercial Ru catalysts. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

Authors
Xu C.1 , Ouyang W.2 , Muñoz-Batista M.J.2 , Fernández-García M.3 , Luque R. 2, 4
Journal
Publisher
Wiley-VCH Verlag
Number of issue
15
Language
English
Pages
2604-2611
Status
Published
Volume
11
Year
2018
Organizations
  • 1 School of Food and Biological Engineering, Zhengzhou University of Light Industry, Dongfeng Road 5, Zhengzhou, Henan 450002, China
  • 2 Departamento de Química Orgánica, Universidad de Córdoba, Edif. Marie Curie, Ctra Nnal IV-A, Km 396, Córdoba, E14014, Spain
  • 3 Instituto de Catálisis y Petroleoquímica, CSIC, Marie Curie 2, Madrid, 28049, Spain
  • 4 Peoples Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya street, Moscow, 117198, Russian Federation
Keywords
biomass; flow chemistry; green chemistry; heterogeneous catalysis; hydrogenation
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/6464/
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