High-Loading Nickel Phosphide Catalysts Supported on SiO2-TiO2 for Hydrodeoxygenation of Guaiacol

被引:38
作者
Zhang, Peng [1 ,2 ]
Sun, Yu [1 ,2 ]
Lu, Mohong [1 ,2 ]
Zhu, Jie [1 ,2 ]
Li, Mingshi [1 ,2 ]
Shan, Yuhua [1 ,2 ]
Shen, Jianyi [3 ]
Song, Chunshan [4 ,5 ]
机构
[1] Changzhou Univ, Jiangsu Key Lab Adv Catalyt Mat & Technol, Adv Catalysis & Green Mfg Collaborat Innovat Ctr, Changzhou 213164, Peoples R China
[2] Changzhou Univ, Sch Petrochem Engn, Changzhou 213164, Peoples R China
[3] Nanjing Univ, Sch Chem & Chem Engn, Lab Mesoscop Chem, Nanjing 210093, Jiangsu, Peoples R China
[4] Penn State Univ, Dept Energy & Mineral Engn, EMS Energy Inst, Clean Fuels & Catalysis Program, 209 Acad Projects Bldg, State Coll, PA 16802 USA
[5] Penn State Univ, Dept Chem Engn, EMS Energy Inst, Clean Fuels & Catalysis Program, 209 Acad Projects Bldg, State Coll, PA 16802 USA
基金
中国国家自然科学基金;
关键词
NI2P CATALYSTS; MODEL-COMPOUND; ATMOSPHERIC HYDRODEOXYGENATION; METHYL LAURATE; OXYGEN-REMOVAL; MIXED OXIDES; HYDRODESULFURIZATION; PHASE; PERFORMANCE; DEOXYGENATION;
D O I
10.1021/acs.energyfuels.9b01538
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
High-loading NixPy catalysts supported on SiO2-TiO2 binary oxides with different Si/Ti atomic ratios were prepared by liquid-phase phosphidation using triphenylphosphine (PPh3) and valued for the hydrodeoxygenation (HDO) of guaiacol. The samples synthesized were characterized by N-2 adsorption, X-ray diffraction (XRD), transmission electron microscopy, X-ray photoelectron spectroscopy (XPS), and ammonia temperature-programmed desorption. The XRD and XPS results showed that the Ni2P/Ni12P5 mixed phase was formed when SiO2-TiO2 binary oxides were employed as supports, whereas only Ni2P and Ni12P5 phases were produced on SiO2 and TiO2 single oxides, respectively. XPS analysis showed that TiO2-x species were generated on the surface of the catalyst during the reduction of the precursor, and the electron transfer occurred from TiO2-x species to the NixPy surface. TiO2-x species on the NixPy surface would contribute to the high HDO activity of guaiacol on NixPy catalysts because the presence of TiO2-x species promoted the adsorption of guaiacol and activation of the C-O bond in the guaiacol molecule. HDO reaction of guaiacol on NixPy catalysts dramatically followed the hydrogenation path owing to the high hydrogenation activity of NixPy catalysts.
引用
收藏
页码:7696 / 7704
页数:9
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