Effect of Zinc on the Structure and Activity of the Cobalt Oxide Catalysts for NO Decomposition

0569340 - ÚCHP 2023 RIV CH eng J - Článek v odborném periodiku
Karásková, K. - Pacultová, K. - Bílková, T. - Fridrichová, D. - Koštejn, Martin - Peikertová, P. - Stelmachowski, P. - Kukula, P. - Obalová, L.
Effect of Zinc on the Structure and Activity of the Cobalt Oxide Catalysts for NO Decomposition.
Catalysts. Roč. 13, č. 1 (2023), č. článku 18. E-ISSN 2073-4344
Institucionální podpora: RVO:67985858
Klíčová slova: nitric oxide * catalytic decomposition * Co-spinel * Zn bulk promotion
Obor OECD: Chemical process engineering
Impakt faktor: 3.9, rok: 2022
Způsob publikování: Open access
https://www.mdpi.com/2073-4344/13/1/18

Co4-iZniMnAlOx mixed oxides (i = 0, 0.5 and 1) were prepared by coprecipitation, subsequently modified with potassium (2 or 4 wt.% K), and investigated for direct catalytic NO decomposition, one of the most attractive and challenging NOx abatement processes. The catalysts were characterised by atomic absorption spectroscopy, powder X-ray diffraction, Raman and infrared spectroscopy, temperature-programmed reduction by hydrogen, the temperature-programmed desorption of CO2 and NO, X-ray photoelectron spectroscopy, scanning electron microscopy, the work function, and N-2 physisorption. The partial substitution of cobalt increased the specific surface area, decreased the pore sizes, influenced the surface composition, and obtained acid-base properties as a result of the higher availability of medium and strong basic sites. No visible changes in the morphology, crystallite size, and work function were observed upon the cobalt substitution. The conversion of NO increased after the Co substitution, however, the increase in the amount of zinc did not affect the catalytic activity, whereas a higher amount of potassium caused a decrease in the NO conversion. The results obtained, which were predominantly the acid-base characteristics of the catalyst, are in direct correlation with the proposed NO decomposition reaction mechanisms with NOx- as the main reaction intermediates.
Trvalý link: https://hdl.handle.net/11104/0340748