4.7 Article

Efficient synthesis of bioetheric fuel additive by combining the reductive and direct etherification of furfural in one-pot over Pd nanoparticles deposited on zeolites

Journal

GREEN ENERGY & ENVIRONMENT
Volume 8, Issue 2, Pages 519-529

Publisher

KEAI PUBLISHING LTD
DOI: 10.1016/j.gee.2021.07.001

Keywords

Etherification; Furfural; Palladium; Zeolite; Amino organosilane

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This study investigates the particle size effect of Pd catalysts on the reductive etherification of furfural. It is found that Pd nanoparticles larger than 3 nm are suitable for one-step reductive etherification. Based on this finding, a Pd/ZSM-5 bifunctional catalyst is prepared by introducing amino organosilane, which successfully achieves one-pot synthesis of ether via reductive etherification and direct etherification, while suppressing undesired side-reactions.
Furfuryl ethers have been considered to be a promising fuel additive. One step reduction etherification of furfural over supported Pd catalysts provides a facile way for the preparation of furfuryl ether. However, the preparation of a reusable Pd catalyst for reductive etherification remains to be a great challenge. In this study, a series of SiO2 supported Pd catalysts with particle size ranging from 2.2 nm to 28 nm were prepared. Their textural properties and catalytic performance in furfural reductive etherification have been systematically studied. The results herein shed light on the particle size effect on the competition between hydrogenation/hydrogenolysis of C=O in furfural over Pd surface. We found out that Pd nanoparticles larger than 3 nm are preferred for one step reductive etherification. Based on this finding, we prepared a Pd/ZSM-5 bifunctional catalyst comprising Pd nanoparticles larger than 3 nm and decreased acidity in presence of amino organosilane, which served as a bifunctional catalyst succeeding in one-pot synthesis of ether via reductive-etherification and direct-etherification. This strategy showed significant advantage in efficiently converting furfuryl acohol, a major side-product, into ether, while suppressing the undesired side-reactions.(c) 2021 Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communi-cations Co., Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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