Hydrogen Production from Biogas: Development of an Efficient Nickel Catalyst by the Exsolution Approach

被引:6
作者
Matus, Ekaterina [1 ]
Kerzhentsev, Mikhail [1 ]
Ismagilov, Ilyas [1 ]
Nikitin, Andrey [1 ]
Sozinov, Sergey [1 ]
Ismagilov, Zinfer [1 ]
机构
[1] RAS, SB, Fed Res Ctr Coal & Coal Chem, Kemerovo 650000, Russia
基金
俄罗斯科学基金会;
关键词
hydrogen; biogas; methane; steam; CO2; reforming; Ni catalyst; exsolution; SYNGAS PRODUCTION; OXIDATIVE DESULFURIZATION; REFORMING REACTION; CARBON DEPOSITION; NI; METHANE; SULFUR; STEAM; LA; BIOHYDROGEN;
D O I
10.3390/en16072993
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
Hydrogen production from biogas over alumina-supported Ce1-xNixO2-x catalysts was studied in a temperature range of 600-850 degrees C with an initial gas composition of CH4/CO2/H2O of 1/0.8/0.4. To achieve a high and stable hydrogen yield, highly dispersed Ni catalysts were prepared through the exsolution approach. A solid solution of Ce1-xNixO2-x was firstly formed on the surface of Al2O3 and then activated in H-2/Ar at 800 degrees C. The genesis and properties of the Ce1-xNixO2-x/Al2O3 catalysts were established using X-ray fluorescence analysis, thermal analysis, N-2 adsorption, ex situ and in situ X-ray diffraction, Raman spectroscopy, electron microscopy, EDX analysis, and temperature-programmed hydrogen reduction. The performance of Ce1-xNixO2-x/Al2O3 catalysts in biogas conversion was tuned by regulation of the dispersion and reducibility of the active component through variation of content (5-20 wt.%) and composition (x = 0.2, 0.5, 0.8) of Ce1-xNixO2-x as well as the mode of its loading (co-impregnation (CI), citrate sol-gel method (SG)). For the 20 wt.% Ce1-xNixO2-x/Al2O3 catalyst, the rate of the coke formation decreased by a factor of 10 as x increased from 0.2 to 0.8. The optimal catalyst composition (20 wt.% Ce0.2Ni0.8O1.8/80 wt.% Al2O3) and preparation mode (citrate sol-gel method) were determined. At 850 degrees C, the 20 wt.% Ce0.2Ni0.8O1.8/Al2O3-SG catalyst provides 100% hydrogen yield at full CH4 conversion and 85% CO2 utilization.
引用
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页数:21
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