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    ZrOCl2 as a bifunctional and in situ precursor material for catalytic hydrogen transfer of bio-based carboxides

    Year: 2020

    Journal: Sustain. Energ. Fuels, Volume 4, JUN 1, page 3102–3114

    Authors: He, Jian; Xu, Yufei; Yu, Zhaozhuo; Li, Hu; Zhao, Wenfeng; Wu, Hongguo; Yang, Song

    Organizations: National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21576059, 21666008, 21908033]; Fok Ying-Tong Education FoundationFok Ying Tung Education Foundation [161030]; Guizhou Science & Technology Foundation [[2018]1037]; outstanding Youth Project of Hunan Provincial Education Department [19B470]

    The effective and economically feasible tandem synthesis of gamma-valerolactone (GVL), a renowned bio-based platform molecule with great promising applications in the production of drop-in chemicals, liquid fuels and polymers, is significantly vital and challenging. Herein, we for the first time describe a direct and effective catalytic system based on ZrOCl2 center dot 8H(2)O capable of facilitating the one-pot one-step tandem synthesis of GVL from bio-based furfural or furfuryl alcohol in 2-propanol by integrating sequential transfer hydrogenation, ring-opening, and transfer hydrogenation-cyclization reactions. A maximum GVL yield of 63.3% and 52.1% was achieved from furfuryl alcohol and furfural at 200 degrees C, respectively. The synergistic effect of [ZrO(OH)(2)](n)center dot xH(2)O species and Bronsted acid species H+, derived from in situ hydrolysis of ZrOCl2 center dot 8H(2)O, is accountable for its remarkable catalytic performance. Moreover, calcination of the leftover solid after tandem synthesis of GVL could fabricate a hollow microrod ZrO2 material, in which the formation of a microrod morphology and hollow structure was probably attributed to the electrostatic repulsion forces among particles in the alcohol solution and removal of generated humins/coke during the reactions within collected solids via calcination, respectively. Importantly, hollow microrod ZrO2 innovatively featuring a high BET surface area, a large amount of acid-base sites and facile active-site accessibility thereby exhibited a superior performance in the catalytic transfer hydrogenation of biomass-derived aldehydes or ketones to ZrO2 prepared by the precipitation method.
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