中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Selective Hydrodeoxygenation of Guaiacol to Phenolics by Ni/Anatase TiO2 Catalyst Formed by Cross-Surface Migration of Ni and TiO2

文献类型:期刊论文

作者Chen, Shanyong5; Kung, Harold H.1; Zhang, Z. Conrad2; Zhang, Xiaoqiang2,3; Yan, Peifang2; Zhao, Bin4; Liu, Kairui2,3; Kung, Mayfair C.1
刊名ACS CATALYSIS
出版日期2019-04-01
卷号9期号:4页码:3551-3563
ISSN号2155-5435
关键词guaiacol hydrodeoxygenation phenol SMSI or strong metal-support interaction titania and nickel lignin
DOI10.1021/acscatal.9b00400
通讯作者Kung, Harold H.(hkung@northwestern.edu) ; Zhang, Z. Conrad(zczhang@yahoo.com)
英文摘要The catalytic properties of physical mixtures of Ni particles (100-200 nm) with nanoparticles of anatase TiO2 (TiO2-A), ZrO2, Al2O3, rutile TiO 2 (TiO2-R), and CeO2 were investigated for the hydrodeoxygenation (HDO) of guaiacol. High selectivities to phenolics were obtained only for Ni mixed with anatase TiO2 (Ni and TiO2-A), while saturated hydro- carbons were the main products for the mixtures with other supports. By thermal treatment in hydrogen gas only at 300 degrees C or higher and subsequently separating the large Ni particles from the TiO2-A particles with a magnet, it was further discovered that there was migration of TiO 2 from TiO2-A onto the large Ni particles, resulting in an amorphous TiO2 overlayer on the Ni particles as evidenced by high-resolution TEM, and vice versa, migration of Ni onto TiO2-A. The TiO2 overlayer rendered the Ni particles completely inactive as a hydrogenation/hydrodeoxygenation catalyst. Conversely, the small amounts of Ni (<1.5 wt %) migrated onto TiO2-A formed highly dispersed Ni, undetectable by high-resolution TEM (<2 nm), that were remarkably highly active for HDO of guaiacol, producing selectively phenolics. Such highly selective HDO catalysts could also be formed by incipient wetness impregnation of Ni in loadings above 2 wt % onto the TiO2-A, but it was essential to pretreat the sample in H-2 at 300 degrees C or higher. Pretreatment in H-2 at 200 degrees C generated catalysts that produced saturated ring products. The activity of the impregnated catalysts, as measured by guaiacol conversion, increased linearly with Ni loading below 0.5 wt %. The activity continued to increase with Ni loading but more slowly up to 2 wt %, beyond which there was little further change. The results suggested that two types of Ni species existed on the TiO2-A surface. One type consisted of a cluster of Ni atoms that were dominant on larger Ni particles that were active in aromatic ring hydrogenation and hydrodeoxygenation. They were readily covered by reducible TiO2-A at 300 degrees C or higher due to the traditional strong metal support interaction (SMSI) effect and became inactive. Another type was clusters of a very small number of Ni atoms, perhaps one atom, that were present as highly dispersed Ni clusters interacting strongly with the defect sites of TiO2-A. The strong interaction of this type of Ni with the TiO2 defect deterred TiO, migration allowing surface exposed Ni atoms to catalyze the HDO of guaiacol with very high selectivities that were not characteristic of typical Ni particles.
WOS关键词METAL-SUPPORT INTERACTIONS ; CO METHANATION ; NI/TIO2 CATALYST ; CARBON NANOTUBES ; BIO-OIL ; LIGNIN ; HYDROGENATION ; CONVERSION ; BIOMASS ; SPILLOVER
资助项目Global Expert program of China ; National Natural Science Foundation of China[21690084] ; National Natural Science Foundation of China[21721004] ; U.S. Department of Energy[DE-FG02-03ER15457]
WOS研究方向Chemistry
语种英语
出版者AMER CHEMICAL SOC
WOS记录号WOS:000464075700082
资助机构Global Expert program of China ; Global Expert program of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; U.S. Department of Energy ; U.S. Department of Energy ; Global Expert program of China ; Global Expert program of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; U.S. Department of Energy ; U.S. Department of Energy ; Global Expert program of China ; Global Expert program of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; U.S. Department of Energy ; U.S. Department of Energy ; Global Expert program of China ; Global Expert program of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; U.S. Department of Energy ; U.S. Department of Energy
源URL[http://cas-ir.dicp.ac.cn/handle/321008/165568]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
通讯作者Kung, Harold H.; Zhang, Z. Conrad
作者单位1.Northwestern Univ, Dept Chem Engn, Evanston, IL 60208 USA
2.Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China
3.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
4.Dalian Univ Technol, Sch Chem Engn, PSU DUT Joint Ctr Energy Res, State Key Lab Fine Chem, Dalian 116024, Peoples R China
5.Nanjing Univ, Sch Chem & Chem Engn, Key Lab Mesoscop Chem MOE, Nanjing 210023, Jiangsu, Peoples R China
推荐引用方式
GB/T 7714
Chen, Shanyong,Kung, Harold H.,Zhang, Z. Conrad,et al. Selective Hydrodeoxygenation of Guaiacol to Phenolics by Ni/Anatase TiO2 Catalyst Formed by Cross-Surface Migration of Ni and TiO2[J]. ACS CATALYSIS,2019,9(4):3551-3563.
APA Chen, Shanyong.,Kung, Harold H..,Zhang, Z. Conrad.,Zhang, Xiaoqiang.,Yan, Peifang.,...&Kung, Mayfair C..(2019).Selective Hydrodeoxygenation of Guaiacol to Phenolics by Ni/Anatase TiO2 Catalyst Formed by Cross-Surface Migration of Ni and TiO2.ACS CATALYSIS,9(4),3551-3563.
MLA Chen, Shanyong,et al."Selective Hydrodeoxygenation of Guaiacol to Phenolics by Ni/Anatase TiO2 Catalyst Formed by Cross-Surface Migration of Ni and TiO2".ACS CATALYSIS 9.4(2019):3551-3563.

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来源:大连化学物理研究所

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