Improving the performance of nickel catalyst supported on mesostructured silica nanoparticles in methanation of CO2-rich gas by urea–nitrate combustion

In this work, NiO supported mesostructured silica nanoparticles (MSN) were synthesized via the urea–nitrate combustion method using urea as fuel and nitrate salts as oxidants with the different urea/nitrate ratios and calcination duration. The physicochemical properties of catalysts were investigate...

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Veröffentlicht in:Chemical papers 2020-11, Vol.74 (11), p.3925-3935
Hauptverfasser: Nguyen, Phung-Anh, Luu, Cam-Loc, Nguyen, Thi-Thuy-Van, Nguyen, Tri, Hoang, Tien-Cuong
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Sprache:eng
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Zusammenfassung:In this work, NiO supported mesostructured silica nanoparticles (MSN) were synthesized via the urea–nitrate combustion method using urea as fuel and nitrate salts as oxidants with the different urea/nitrate ratios and calcination duration. The physicochemical properties of catalysts were investigated by several techniques, including N 2 physisorption measurements, powder X-ray diffraction, N 2 -BET isothermal adsorption, hydrogen temperature-programmed reduction, carbon dioxide temperature-programmed desorption, scanning electron microscopy and transmission electron microscopy. The obtained catalysts were employed in the methanation of CO 2 -rich gas at a temperature range of 225–400 °C with the CO 2 /H 2 ratio of 1/4 and CO 2 concentration of 20 mol%. The results showed that using the urea–nitrate combustion method in synthesizing catalysts led to improved physicochemical properties that increased the activity of NiO/MSN catalysts. The catalyst prepared with the urea/nitrate molar ratio of 3 and calcined at 600 °C for 3 h showed the highest catalytic performance in methanation of CO 2 -rich gas, reaching CO 2 conversion of 96% and CH 4 selectivity of 100% at 375 °C. The best catalyst has excellent stability in CO 2 solo-hydrogenation at a reaction temperature of 375 °C during 30 h of reaction thanks to the resistance to coke formation. Besides, adding 1 mol% CO in the feedstock should be simultaneously conducted to surge the effectivity of CO 2 methanation.
ISSN:2585-7290
0366-6352
1336-9075
DOI:10.1007/s11696-020-01207-0