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在镧促进的镍/氧化锆催化剂上生物质衍生的山梨醇的氢解反应

Hydrogenolysis of biomass-derived sorbitol over La-promoted Ni/ZrO catalysts.

作者信息

Cai Chiliu, Wang Haiyong, Xin Haosheng, Zhu Changhui, Zhang Qi, Zhang Xinghua, Wang Chenguang, Liu Qiying, Ma Longlong

机构信息

Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences 510640 Guangzhou China

Key Laboratory of Renewable Energy, Chinese Academy of Sciences 510640 Guangzhou China.

出版信息

RSC Adv. 2020 Jan 23;10(7):3993-4001. doi: 10.1039/c9ra10394e. eCollection 2020 Jan 22.

DOI:10.1039/c9ra10394e
PMID:35492633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9048756/
Abstract

Ni/LaO/ZrO catalysts were prepared by a step-by-step impregnation method through regulation of the contents of the active component and alkali. The introduction of an alkaline promoter not only enhanced the alkalinity of the catalyst but also improved the dispersion of Ni on the catalyst owing to the strong interaction between Ni and alkali promoter. The synergistic effect between Ni and LaO was beneficial to selective hydrogenolysis of sorbitol. Under the optimal reaction conditions, sorbitol conversion reached nearly 100% and target products (ethylene glycol, 1,2-propanediol, and glycerol) selectivity reached 74.8%. Metal-alkali coordination mechanism and possible pathways for target products formation were proposed.

摘要

通过逐步浸渍法,通过调节活性组分和碱的含量制备了Ni/LaO/ZrO催化剂。碱性助剂的引入不仅增强了催化剂的碱性,还由于Ni与碱性助剂之间的强相互作用提高了Ni在催化剂上的分散度。Ni与LaO之间的协同作用有利于山梨醇的选择性氢解。在最佳反应条件下,山梨醇转化率接近100%,目标产物(乙二醇、1,2-丙二醇和甘油)选择性达到74.8%。提出了金属-碱配位机理和目标产物形成的可能途径。

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Angew Chem Int Ed Engl. 2012 Mar 12;51(11):2564-601. doi: 10.1002/anie.201105125. Epub 2012 Feb 28.
3
Transformations of biomass-derived platform molecules: from high added-value chemicals to fuels via aqueous-phase processing.
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4
Catalytic conversion of biomass to monofunctional hydrocarbons and targeted liquid-fuel classes.生物质向单官能烃类和目标液体燃料类别的催化转化。
Science. 2008 Oct 17;322(5900):417-21. doi: 10.1126/science.1159210. Epub 2008 Sep 18.
5
Liquid-phase catalytic processing of biomass-derived oxygenated hydrocarbons to fuels and chemicals.生物质衍生含氧烃类的液相催化加工制燃料和化学品
Angew Chem Int Ed Engl. 2007;46(38):7164-83. doi: 10.1002/anie.200604274.
6
Synthesis of transportation fuels from biomass: chemistry, catalysts, and engineering.生物质合成运输燃料:化学、催化剂与工程
Chem Rev. 2006 Sep;106(9):4044-98. doi: 10.1021/cr068360d.