Catalytic activities of titania-supported nickel for carbon-dioxide methanation

被引:36
|
作者
Unwiset, Preeya [1 ,2 ]
Chanapattharapol, Kingkaew Chayakul [1 ,2 ]
Kidkhunthod, Pinit [3 ]
Poo-arporn, Yingyot [3 ]
Ohtani, Bunsho [4 ]
机构
[1] Khon Kaen Univ, Fac Sci, Mat Chem Res Ctr, Dept Chem, Khon Kaen 40002, Thailand
[2] Khon Kaen Univ, Fac Sci, Ctr Excellence Innovat Chem, Khon Kaen 40002, Thailand
[3] Synchrotron Light Res Inst, 111 Univ Ave, Muang Dist 30000, Nakhon Ratchasi, Thailand
[4] Hokkaido Univ, Inst Catalysis, Sapporo, Hokkaido 0010021, Japan
关键词
Carbon-dioxide methanation; Titania-supported nickel; XANES; EXAFS; CO2; METHANATION; PARTICLE-SIZE; TIO2; HYDROGENATION; PERFORMANCE; VACANCIES; XANES; STATE; ZNO; H-2;
D O I
10.1016/j.ces.2020.115955
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Titania-supported nickel catalysts (3, 6, 12 and 20 wt% Ni/TiO2) were prepared by a sol-gel method. The results showed that the CO2 conversion increased with increasing Ni content and 20 wt% Ni/TiO2 exhibited the highest CO2 conversion and CH4 yield. The results on XRD and EXAFS revealed unit cell expansion and lattice distortion, which indicated that Ni2+ was incorporated into the TiO2 lattice. Upon increasing the Ni content, the NiO phase was observed. The oxidation states of nickel and titanium were analyzed to be +2 and +4, respectively for fresh catalysts. After pretreatment by H-2, Ni2+ was converted to Ni-0 and this electronic state remained unchanged during the course of methanation while Ti4+ was kept unaltered for fresh catalysts and those during the reaction. The addition of Ni led to the formation of oxygen vacancy and NiO phase which might act as adsorption sites for CO2 and H-2, respectively. (C) 2020 Elsevier Ltd. All rights reserved.
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页数:19
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