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One-pot selective production of deoxygenated monomeric, dimeric, and trimeric hydrocarbons from xylose-derived 2-methylfuran using multifunctional tungstate-zirconia-supported Ru, Pd, and Ni catalystsopen access

Authors
Jo, HyeonminChoo, HyunahChoi, Jae-WookSuh, Dong JinYoo, Chun-JaeKim, Chang SooKim, Kwang HoLee, HyunjooKim, KyeongsuChoi, JungkyuHa, Jeong-Myeong
Issue Date
1-Aug-2022
Publisher
ELSEVIER SCIENCE SA
Keywords
One-pot three-step process; Condensation; Hydrodeoxygenation; Multifunctional catalysts; 2-Methylfuran; Iso-pentadecane
Citation
CHEMICAL ENGINEERING JOURNAL, v.441
Indexed
SCIE
SCOPUS
Journal Title
CHEMICAL ENGINEERING JOURNAL
Volume
441
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/143328
DOI
10.1016/j.cej.2022.135581
ISSN
1385-8947
Abstract
The multifunctionality of tungstate-zirconia-supported metal catalysts was demonstrated in a three-step conversion of 2-methylfuran (2-MF) into deoxygenated C10-15 hydrocarbon fuels in a one-pot reactor, with condensation, hydrogenation, and hydrodeoxygenation performed using single tungstate-zirconia-supported metal catalysts. Manipulation of the reaction conditions, in particular, the reaction temperature and feeding reactant for each reaction step, enabled different catalytic functions of the tungstate-zirconia-supported metals at different reaction stages. Among the metals, Ni favored the production of C-10 hydrocarbons by suppressing further condensation to C-15 compounds, whereas Ru favored the trimerization of 2-MF during the condensation step to produce C-15 hydrocarbons. The superior hydrogenation of 2-MF on Pd reduced the formation of C10-15 compounds. The acidity and hydrogenation activity of the catalysts were investigated to demonstrate the multifunctionality of tungstate-zirconia-supported metals. The catalysts were characterized using H-2 temperature programmed reduction, H-2 temperature programmed desorption, X-ray diffraction, transmission electron microscopy, and nuclear magnetic resonance; the results confirmed the variations in their activity among the different reactions.
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