Mn–Fe bi-metal oxides in situ created on metal wire mesh as monolith catalysts for selective catalytic reduction of NO with NH3. Issue 64 (18th August 2017)
- Record Type:
- Journal Article
- Title:
- Mn–Fe bi-metal oxides in situ created on metal wire mesh as monolith catalysts for selective catalytic reduction of NO with NH3. Issue 64 (18th August 2017)
- Main Title:
- Mn–Fe bi-metal oxides in situ created on metal wire mesh as monolith catalysts for selective catalytic reduction of NO with NH3
- Authors:
- Liu, Jie
Kang, Lin
Li, Hongrui
Maitarad, Phornphimon
Zhang, Jianping
Shi, Liyi
Zhang, Dengsong - Abstract:
- Abstract : Mn–Fe bi-metal oxides in situ created on a metal wire mesh are demonstrated as high-performance deNO x monolith catalysts. Abstract : In this work, we use an Fe wire mesh to provide homogeneous nucleation sites to support a continuous in situ growth of Mn–Fe bi-metal oxides as monolith catalysts for selective catalytic reduction of NO with NH3 . The strategy of a "twin iron source" makes the Mn–Fe seeds easily grow on the Fe wire mesh through the surface Fe metal sites rather than free growth. The Fe wire mesh exhibited excellent affinity properties with Mn–Fe hydroxides precursor. Through the calcination treatment, a spinel structure of Mn–Fe bi-metal oxides coated monolithic catalyst was prepared and used for denitrification. By adjusting the ratio of the Mn–Fe precursors, we obtained Mn–Fe bi-metal oxides with various morphologies coated on the surface of Fe wire mesh. Impressively, the cube-like Mn–Fe bi-metal oxides structure on the Fe wire mesh as monolith catalysts exhibited high De-NO x performance, catalytic activity, stability, H2 O tolerance, K + poisoning resistance and regeneration performance. The results showed that the spinel structure of Mn–Fe bi-metal oxides in the coating layer was the critical factor for enhanced adsorption behaviours and reducibilities, which promoted selective catalytic reduction of NO with NH3 . The good adhesion between the Mn–Fe spinel and Fe wire mesh contributed to the super stability and the strong adsorption propertiesAbstract : Mn–Fe bi-metal oxides in situ created on a metal wire mesh are demonstrated as high-performance deNO x monolith catalysts. Abstract : In this work, we use an Fe wire mesh to provide homogeneous nucleation sites to support a continuous in situ growth of Mn–Fe bi-metal oxides as monolith catalysts for selective catalytic reduction of NO with NH3 . The strategy of a "twin iron source" makes the Mn–Fe seeds easily grow on the Fe wire mesh through the surface Fe metal sites rather than free growth. The Fe wire mesh exhibited excellent affinity properties with Mn–Fe hydroxides precursor. Through the calcination treatment, a spinel structure of Mn–Fe bi-metal oxides coated monolithic catalyst was prepared and used for denitrification. By adjusting the ratio of the Mn–Fe precursors, we obtained Mn–Fe bi-metal oxides with various morphologies coated on the surface of Fe wire mesh. Impressively, the cube-like Mn–Fe bi-metal oxides structure on the Fe wire mesh as monolith catalysts exhibited high De-NO x performance, catalytic activity, stability, H2 O tolerance, K + poisoning resistance and regeneration performance. The results showed that the spinel structure of Mn–Fe bi-metal oxides in the coating layer was the critical factor for enhanced adsorption behaviours and reducibilities, which promoted selective catalytic reduction of NO with NH3 . The good adhesion between the Mn–Fe spinel and Fe wire mesh contributed to the super stability and the strong adsorption properties of NH3, which made it dominant in the NH3 adsorption process competing with water. The obtained monolith catalysts showed good resistances to K + poisoning and good regeneration performance, which can be attributed to the structural stability of Mn–Fe spinel and strong synergistic effect between the support and active species. This new kind of monolithic catalyst prepared by an in situ technique can be used as a potential substitute for vanadium based ceramic catalysts. … (more)
- Is Part Of:
- RSC advances. Volume 7:Issue 64(2017)
- Journal:
- RSC advances
- Issue:
- Volume 7:Issue 64(2017)
- Issue Display:
- Volume 7, Issue 64 (2017)
- Year:
- 2017
- Volume:
- 7
- Issue:
- 64
- Issue Sort Value:
- 2017-0007-0064-0000
- Page Start:
- 40444
- Page End:
- 40451
- Publication Date:
- 2017-08-18
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7ra05007k ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4479.xml