Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/54992
Title: Effect of NO2 and NO3-/HNO3 adsorption on NO photocatalytic conversion
Authors: Araña, J. 
Garzón Sousa, D. 
González Díaz, O. 
Pulido Melián, E. 
Doña Rodríguez, J. M. 
UNESCO Clasification: 221001 Catálisis
Keywords: Selective Catalytic-Reduction
Nitric-Oxide
Nitrogen-Dioxide
Molecular-Sieve
Tio2, et al
Issue Date: 2019
Project: Eliminacion Fotocatalitica de Mezclas de Nox y Covs en Emisiones Gaseosas Con Ti02 y Oxidos Mixtos. 
Hormigones Fotocatalíticos 
Investigación de Las Interacciones de Los Nox Sobre Semiconductores Soportados En 
Journal: Applied Catalysis B: Environmental 
Abstract: A study was undertaken of the adsorption and photocatalytic conversion of NO, NO2 and NO3-/HNO3 using two photocatalysts (P25 and HT-ET). The HT-ET is a catalyst synthesized in our laboratory comprised only of anatase phase and with a surface area three times larger than that of the P25. In powder form, the catalyst was introduced into and extended along the length of a tube with no type of compaction on the part of the solid (pressure drops are negligible under these conditions). This tubular photoreactor arrangement operates as a continuous reactor system enabling FTIR analysis of the surface of the catalysts during the conversion process. NO adsorption was negligible, though the FTIR studies revealed the formation of nitrites on the surface after 18 h of reaction. Overall NO conversion efficiency rates were above 68% with both catalysts in that reaction time. However, selectivity to NO2 was very high with both catalysts. It was also found with both catalysts that the number of NOx moles eliminated during NO photocatalytic conversion coincided with the number of adsorbed NO2 moles observed in the adsorption studies performed with this molecule, indicating that the NO2 molecule is not efficiently converted photocatalytically.
URI: http://hdl.handle.net/10553/54992
ISSN: 0926-3373
DOI: 10.1016/j.apcatb.2018.12.005
Source: Applied Catalysis B: Environmental [ISSN 0926-3373], v. 244, p. 660-670
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