Number of the records: 1
Magnesium E ect in K/Co-Mg-Mn-Al Mixed Oxide Catalyst for Direct NO Decomposition.
- 1.0540443 - ÚCHP 2021 RIV CH eng J - Journal Article
Karásková, K. - Pacultová, K. - Klegová, A. - Fridrichová, D. - Valášková, M. - Jirátová, Květa - Stelmachowski, P. - Kotarba, A. - Obalová, L.
Magnesium E ect in K/Co-Mg-Mn-Al Mixed Oxide Catalyst for Direct NO Decomposition.
Catalysts. Roč. 10, č. 8 (2020), č. článku 931. ISSN 2073-4344. E-ISSN 2073-4344
R&D Projects: GA ČR(CZ) GA18-19519S
Institutional support: RVO:67985858
Keywords : cobalt mixed oxide * alkali promoter * nitric oxide * catalytic decomposition
OECD category: Chemical process engineering
Impact factor: 4.146, year: 2020
Method of publishing: Open access
file:///C:/Users/jirsova/AppData/Local/Temp/catalysts-10-00931.pdf
Emission of nitric oxide represents a serious environmental problem since it contributes to the formation of acid rain and photochemical smog. Potassium-modified Co-Mn-Al mixed oxide is an effective catalyst for NO decomposition. However, there are problems related to the thermal instability of potassium species and a high content of toxic and expensive cobalt. The reported research aimed to determine whether these shortcomings can be overcome by replacing cobalt with magnesium. Therefore, a series of Co-Mg-Mn-Al mixed oxides with different Co/Mg molar ratio and promoted by various content of potassium was investigated. The catalysts were thoroughly characterized by atomic absorption spectroscopy (AAS), temperature-programmed reduction by hydrogen (TPR-H2), temperature-programmed desorption of CO2 (TPD-CO2), X-ray powder diffraction (XRD), N2 physisorption, species-resolved thermal alkali desorption (SR-TAD), and tested in direct NO decomposition with and without the addition of oxygen and water vapor. Partial substitution of magnesium for cobalt did not cause an activity decrease when the optimal molar ratio of K/Co on the normalized surface area was maintained. It means that the portion of expensive and toxic cobalt can be successfully replaced by magnesium without any decrease in catalytic activity.
Permanent Link: http://hdl.handle.net/11104/0318048
File Download Size Commentary Version Access catalysts-10-00931.pdf 0 5.5 MB Publisher’s postprint open-access
Number of the records: 1