Les Inscriptions à la Bibliothèque sont ouvertes en
ligne via le site: https://biblio.enp.edu.dz
Les Réinscriptions se font à :
• La Bibliothèque Annexe pour les étudiants en
2ème Année CPST
• La Bibliothèque Centrale pour les étudiants en Spécialités
A partir de cette page vous pouvez :
Retourner au premier écran avec les recherches... |
Détail de l'auteur
Auteur Yuntao Li
Documents disponibles écrits par cet auteur
Affiner la rechercheNO (or NH3) + O2 adsorption on fluorine-doped vanadia/titania and its role in the mechanism of a two - step process characterized by EPR / Qin Zhong in Chemical engineering journal, Vol. 174 N° 1 (Octobre 2011)
[article]
in Chemical engineering journal > Vol. 174 N° 1 (Octobre 2011) . - pp.390–395
Titre : NO (or NH3) + O2 adsorption on fluorine-doped vanadia/titania and its role in the mechanism of a two - step process characterized by EPR Type de document : texte imprimé Auteurs : Qin Zhong, Auteur ; Tianjiao Zhang, Auteur ; Yuntao Li, Auteur Année de publication : 2012 Article en page(s) : pp.390–395 Note générale : Génie chimique Langues : Anglais (eng) Mots-clés : Low-temperature selective catalytic reduction F-doping Vanadia/titania Superoxide ions Résumé : This study aimed at elucidating a two-step process of the low-temperature selective catalytic reduction (SCR) reaction. The data were collected through studying the EPR signal of NO (or NH3) + O2 adsorption on fluorine-doped vanadia/titania and vanadia/titania catalysts used for SCR reaction, as well as the impact of SO2 and H2O added to the gas mixtures. The EPR experiments provided a new method to explain the SCR reaction, which were associated with NO (NH3) + O2 reacting systems and had been inferred step by step. In summary, the first step of the two-step process was that the vanadium sites were reduced by NO or NH3 as electron donor; then, the superoxide ions appeared over vanadium.
The experimental findings showed that the surface acidity, surface oxygen vacancies and the superoxide could be increased by fluorine doping, accordingly, the two-step process rate would be enhanced by F doping. It was the reason for F-doped catalyst had the higher catalytic activity than vanadia/titania. This two-step process could also be used to elucidate the inhibition mechanism of SO2 and H2O for the SCR reaction.ISSN : 1385-8947 En ligne : http://www.sciencedirect.com/science/article/pii/S1385894711010734 [article] NO (or NH3) + O2 adsorption on fluorine-doped vanadia/titania and its role in the mechanism of a two - step process characterized by EPR [texte imprimé] / Qin Zhong, Auteur ; Tianjiao Zhang, Auteur ; Yuntao Li, Auteur . - 2012 . - pp.390–395.
Génie chimique
Langues : Anglais (eng)
in Chemical engineering journal > Vol. 174 N° 1 (Octobre 2011) . - pp.390–395
Mots-clés : Low-temperature selective catalytic reduction F-doping Vanadia/titania Superoxide ions Résumé : This study aimed at elucidating a two-step process of the low-temperature selective catalytic reduction (SCR) reaction. The data were collected through studying the EPR signal of NO (or NH3) + O2 adsorption on fluorine-doped vanadia/titania and vanadia/titania catalysts used for SCR reaction, as well as the impact of SO2 and H2O added to the gas mixtures. The EPR experiments provided a new method to explain the SCR reaction, which were associated with NO (NH3) + O2 reacting systems and had been inferred step by step. In summary, the first step of the two-step process was that the vanadium sites were reduced by NO or NH3 as electron donor; then, the superoxide ions appeared over vanadium.
The experimental findings showed that the surface acidity, surface oxygen vacancies and the superoxide could be increased by fluorine doping, accordingly, the two-step process rate would be enhanced by F doping. It was the reason for F-doped catalyst had the higher catalytic activity than vanadia/titania. This two-step process could also be used to elucidate the inhibition mechanism of SO2 and H2O for the SCR reaction.ISSN : 1385-8947 En ligne : http://www.sciencedirect.com/science/article/pii/S1385894711010734