Preparation and characterization of Ni–Co/SiO2 nanocomposite catalysts for CO2 methanation

For effective CO 2 methanation, monometallic Co(10)/SiO 2 and Ni(10)/SiO 2 and bimetallic Ni(5)Co(5)/SiO 2 and Ni(2)Co(8)/SiO 2 nanocomposite (NC) catalysts, where numbers between brackets indicate the metal content (wt%), have been prepared with solvate-stimulated modification, thermal decompositio...

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Bibliographic Details
Published inApplied nanoscience Vol. 12; no. 3; pp. 349 - 359
Main Authors Dyachenko, Аlla G., Ischenko, Olena V., Goncharuk, Olena V., Borysenko, Mykola V., Mischanchuk, Olexandr V., Gun’ko, Volodymyr M., Sternik, Dariusz, Lisnyak, Vladyslav V.
Format Journal Article
LanguageEnglish
Published Cham Springer International Publishing 01.03.2022
Springer Nature B.V
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Summary:For effective CO 2 methanation, monometallic Co(10)/SiO 2 and Ni(10)/SiO 2 and bimetallic Ni(5)Co(5)/SiO 2 and Ni(2)Co(8)/SiO 2 nanocomposite (NC) catalysts, where numbers between brackets indicate the metal content (wt%), have been prepared with solvate-stimulated modification, thermal decomposition, and chemical reduction stages using nanosilica A-300 as a carrier. The catalysts were characterized using SEM–EDX, nitrogen physisorption, and X-ray powder diffraction. The samples before and after the reduction with hydrogen have a similar mesoporous texture. The bimetallic Ni–Co/SiO 2 NC catalysts showed improved catalytic activity compared to Ni/SiO 2 . The formers are characterized by the smallest bimetallic crystallites of ca. 12 nm in size. Activity in the methanation of the Ni–Co/SiO 2 NC catalysts depends on the cobalt content resulting in a prominent increase in CO 2 conversion and methane yield at 250–350 °C. The SEM–EDX analysis showed unusual flower-like nanostructures and proved the random distribution of Ni/Co bimetallic aggregates in the nanosilica matrix at the nanoscale level. Both Ni(2)Co(8)/SiO 2 and Ni(5)Co(5)/SiO 2 exhibited high activity in the CO 2 methanation with 81–88% CH 4 yield at 450 °C. The results of thermo-programmed desorption mass spectroscopy revealed that the catalytic reaction is passed through the formation of O-containing intermediates bound to the active Ni–Co and nanosilica sites.
ISSN:2190-5509
2190-5517
DOI:10.1007/s13204-020-01650-1