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Precipitated K-Promoted Co–Mn–Al Mixed Oxides for Direct NO Decomposition: Preparation and Properties.

Authors :
Jirátová, Květa
Pacultová, Kateřina
Balabánová, Jana
Karásková, Kateřina
Klegová, Anna
Bílková, Tereza
Jandová, Věra
Koštejn, Martin
Martaus, Alexandr
Kotarba, Andrzej
Obalová, Lucie
Source :
Catalysts (2073-4344); Jul2019, Vol. 9 Issue 7, p592-592, 1p
Publication Year :
2019

Abstract

Direct decomposition of nitric oxide (NO) proceeds over Co–Mn–Al mixed oxides promoted by potassium. In this study, answers to the following questions have been searched: Do the properties of the K-promoted Co–Mn–Al catalysts prepared by different methods differ from each other? The K-precipitated Co–Mn–Al oxide catalysts were prepared by the precipitation of metal nitrates with a solution of K<subscript>2</subscript>CO<subscript>3</subscript>/KOH, followed by the washing of the precipitate to different degrees of residual K amounts, and by cthe alcination of the precursors at 500 °C. The properties of the prepared catalysts were compared with those of the best catalyst prepared by the K-impregnation of a wet cake of Co–Mn–Al oxide precursors. The solids were characterized by chemical analysis, DTG, XRD, N<subscript>2</subscript> physisorption, FTIR, temperature programmed reduction (H<subscript>2</subscript>-TPR), temperature programmed CO<subscript>2</subscript> desorption (CO<subscript>2</subscript>-TPD), X-ray photoelectron spectrometry (XPS), and the species-resolved thermal alkali desorption method (SR-TAD). The washing of the K-precipitated cake resulted in decreasing the K amount in the solid, which affected the basicity, reducibility, and non-linearly catalytic activity in NO decomposition. The highest activity was found at ca 8 wt.% of K, while that of the best K-impregnated wet cake catalyst was at about 2 wt.% of K. The optimization of the cake washing conditions led to a higher catalytic activity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20734344
Volume :
9
Issue :
7
Database :
Complementary Index
Journal :
Catalysts (2073-4344)
Publication Type :
Academic Journal
Accession number :
138008651
Full Text :
https://doi.org/10.3390/catal9070592