Study of Ni, Pt, and Ru catalysts on wood‐based activated carbon supports and their activity in furfural conversion to 2‐methylfuran
|Author:||Mäkelä, Eveliina1; Lahti, Riikka2,3; Jaatinen, Salla1;|
1Department of Chemical and Metallurgical Engineering, Aalto University, Aalto, Finland
2Department of Chemistry, University of Oulu, Oulu, Finland
3Kokkola University Consortium Chydenius, University of Jyväskylä, Kokkola, Finland
|Online Access:||PDF Full Text (PDF, 2.2 MB)|
|Persistent link:|| http://urn.fi/urn:nbn:fi-fe2018060525325
John Wiley & Sons,
|Publish Date:|| 2019-04-25
Bio‐based chemicals can be produced from furfural through hydrotreatment. In this study, 2‐methylfuran (MF), a potential biofuel component, was produced with Pt, Ru, and Ni catalysts supported on wood‐based activated carbons. The catalytic hydrotreatment experiments were conducted in a batch reactor at 210–240 °C with 2‐propanol as solvent and 40 bar H₂ pressure. Two types of activated carbon supports were prepared by carbonization and activation of lignocellulosic biomass (forest‐residue‐based birch and spruce from Finland). Both types of activated carbons were suitable as catalyst supports, giving up to 100 % furfural conversions. The most important factors affecting the MF yield were the metal dispersion and particle size as well as reaction temperature. The highest observed MF yields were achieved with the noble metal catalysts with the highest dispersions at 240 °C after 120 min reaction time: 3 wt % Pt on spruce (MF yield of 50 %) and 3 wt % Ru on birch (MF yield of 49 %). Nickel catalysts were less active most likely owing to lower dispersions and incomplete metal reduction. Interesting results were obtained also with varying the metal loadings: the lower Pt loading (1.5 wt %) achieved almost the same MF yield as the 3 wt % catalysts, which can enable the production of MF with high yields and reduced catalyst costs. Based on this study, biomass‐based renewable activated carbons can be used as catalyst supports in furfural hydrotreatment with high conversions.
|Pages:||3269 - 3283|
|Type of Publication:||
A1 Journal article – refereed
|Field of Science:||
116 Chemical sciences
Authors E. Mäkelä and S. Jaatinen acknowledge KAUTE foundation for financial support for this research paper. Author R. Lahti acknowledges the EU/European Regional Development Fund, Leverage from the EU program (within project no. A71029) for financial support.
© 2018 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim. This is the peer reviewed version of the following article: E. Mäkelä, R. Lahti, S. Jaatinen, H. Romar, T. Hu, R. L. Puurunen, U. Lassi, R. Karinen, ChemCatChem 2018, 10, 3269. doi:10.1002/cctc.201800263 which has been published in final form at https://doi.org/10.1002/cctc.201800263. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.