Characterization and catalytic activity of soft-templated NiO-CeO2 mixed oxides for CO and CO2 co-methanation

被引:23
|
作者
Atzori, Luciano [1 ]
Cutrufello, Maria Giorgia [1 ]
Meloni, Daniela [1 ]
Onida, Barbara [2 ]
Gazzoli, Delia [3 ]
Ardu, Andrea [1 ]
Monaci, Roberto [1 ]
Sini, Maria Franca [1 ]
Rombi, Elisabetta [1 ]
机构
[1] Univ Cagliari, Dept Chem & Geol Sci, I-09042 Monserrato, CA, Italy
[2] Politecn Torino, Dept Mat Sci & Chem Engn, CR INSTM Mat Controlled Poros, I-10129 Turin, Italy
[3] Univ Roma La Sapienza, Dept Chem, I-00185 Rome, Italy
关键词
soft template method; NiO-CeO2; catalysts; CO and CO2 co-methanation; synthetic natural gas production; RAY PHOTOELECTRON-SPECTROSCOPY; NATURAL-GAS PRODUCTION; CARBON-DIOXIDE; OXIDATION-STATE; SURFACE; NI; NICKEL; CERIA; METAL; CEO2;
D O I
10.1007/s11705-020-1951-8
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Nanosized NiO, CeO(2)and NiO-CeO(2)mixed oxides with different Ni/Ce molar ratios were prepared by the soft template method. All the samples were characterized by different techniques as to their chemical composition, structure, morphology and texture. On the catalysts submitted to the same reduction pretreatment adopted for the activity tests the surface basic properties and specific metal surface area were also determined. NiO and CeO(2)nanocrystals of about 4 nm in size were obtained, regardless of the Ni/Ce molar ratio. The Raman and X-ray photoelectron spectroscopy results proved the formation of defective sites at the NiO-CeO(2)interface, where Ni species are in strong interaction with the support. The microcalorimetric and Fourier transform infrared analyses of the reduced samples highlighted that, unlike metallic nickel, CeO(2)is able to effectively adsorb CO2, forming carbonates and hydrogen carbonates. After reduction in H(2)at 400 degrees C for 1 h, the catalytic performance was studied in the CO and CO(2)co-methanation reaction. Catalytic tests were performed at atmospheric pressure and 300 degrees C, using CO/CO2/H(2)molar compositions of 1/1/7 or 1/1/5, and space velocities equal to 72000 or 450000 cm(3)center dot h(-1)center dot g(cat)(-1). Whereas CO was almost completely hydrogenated in any investigated experimental conditions, CO(2)conversion was strongly affected by both the CO/CO2/H(2)ratio and the space velocity. The faster and definitely preferred CO hydrogenation was explained in the light of the different mechanisms of CO and CO(2)methanation. On a selected sample, the influence of the reaction temperature and of a higher number of space velocity values, as well as the stability, were also studied. Provided that the Ni content is optimized, the NiCe system investigated was very promising, being highly active for the CO(x)co-methanation reaction in a wide range of operating conditions and stable (up to 50 h) also when submitted to thermal stress.
引用
收藏
页码:251 / 268
页数:18
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