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用于将愈创木酚选择性加氢脱氧制备环己醇的钴-石墨烯催化剂

Cobalt-Graphene Catalyst for Selective Hydrodeoxygenation of Guaiacol to Cyclohexanol.

作者信息

Guo Qichang, Mao Jingbo, Li Shenmin, Yin Jingmei, Lv Yang, Zhou Jinxia

机构信息

College of Environmental and Chemical Engineering, Dalian University, Dalian 116622, China.

出版信息

Nanomaterials (Basel). 2022 Sep 28;12(19):3388. doi: 10.3390/nano12193388.

DOI:10.3390/nano12193388
PMID:36234516
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9565367/
Abstract

Herein, cobalt-reduced graphene oxide (rGO) catalyst was synthesized with a practical impregnation-calcination approach for the selective hydrodeoxygenation (HDO) of guaiacol to cyclohexanol. The synthesized Co/rGO was characterized by transmission electron microscopy (TEM), high-angle annular dark-field scanning TEM (HAADF-STEM), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, X-ray diffraction (XRD), and H temperature-programmed reduction (H-TPR) analysis. According to the comprehensive characterization results, the catalyst contains single Co atoms in the graphene matrix and Co oxide nanoparticles (CoO) on the graphene surface. The isolated Co atoms embedded in the rGO matrix form stable metal carbides (CoC), which constitute catalytically active sites for hydrogenation. The rGO material with proper amounts of N heteroatoms and lattice defects becomes a suitable graphene material for fabricating the catalyst. The Co/rGO catalyst without prereduction treatment leads to the complete conversion of guaiacol with 93.2% selectivity to cyclohexanol under mild conditions. The remarkable HDO capability of the Co/rGO catalyst is attributed to the unique metal-acid synergy between the CoC sites and the acid sites of the CoO nanoparticles. The CoC sites provide H while the acid sites of CoO nanoparticles bind the C-O group of reactants to the surface, allowing easier C-O scission. The reaction pathways were characterized based on the observed reaction-product distributions. The effects of the process parameters on catalyst preparation and the HDO reaction, as well as the reusability of the catalyst, were systematically investigated.

摘要

在此,采用实际的浸渍-煅烧方法合成了钴还原氧化石墨烯(rGO)催化剂,用于将愈创木酚选择性加氢脱氧(HDO)为环己醇。通过透射电子显微镜(TEM)、高角度环形暗场扫描TEM(HAADF-STEM)、X射线光电子能谱(XPS)、拉曼光谱、X射线衍射(XRD)和H程序升温还原(H-TPR)分析对合成的Co/rGO进行了表征。根据综合表征结果,该催化剂在石墨烯基质中包含单个Co原子,在石墨烯表面包含Co氧化物纳米颗粒(CoO)。嵌入rGO基质中的孤立Co原子形成稳定的金属碳化物(CoC),其构成氢化的催化活性位点。具有适量N杂原子和晶格缺陷的rGO材料成为制备该催化剂的合适石墨烯材料。未经预还原处理的Co/rGO催化剂在温和条件下可使愈创木酚完全转化,对环己醇的选择性为93.2%。Co/rGO催化剂卓越的HDO能力归因于CoC位点与CoO纳米颗粒酸性位点之间独特的金属-酸协同作用。CoC位点提供H,而CoO纳米颗粒的酸性位点将反应物的C-O基团结合到表面,使C-O断裂更容易。基于观察到的反应产物分布对反应途径进行了表征。系统研究了工艺参数对催化剂制备和HDO反应的影响以及催化剂的可重复使用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fde/9565367/7f5884c2d9cc/nanomaterials-12-03388-g009.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fde/9565367/49c957d08d84/nanomaterials-12-03388-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fde/9565367/63bbceb5dc93/nanomaterials-12-03388-sch002.jpg
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