Gold Stabilized with Iridium on Ceria-Niobia Catalyst: Activity and Stability for CO Oxidation

被引:11
|
作者
Aguirre, Alejo [1 ,2 ]
Zanella, Rodolfo [3 ]
Barrios, Celina [1 ,2 ]
Hernandez, Sandra [4 ]
Bonivardi, Adrian [1 ,2 ,5 ]
Collins, Sebastian E. [1 ,2 ,5 ]
机构
[1] Univ Nacl Litoral, Inst Desarrollo Tecnol Ind Quim INTEC, Gtiemes 3450, RA-3000 Santa Fe, Argentina
[2] Consejo Nacl Invest Cient & Tecn, Gtiemes 3450, RA-3000 Santa Fe, Argentina
[3] Univ Nacl Autonoma Mexico, Inst Ciencias Aplicadas & Tecnol, Circuito Exterior S-N,Ciudad Univ, Mexico City 04510, DF, Mexico
[4] UNGS, Inst Ind IDEI, Juan M Gutierrez 1150,B1613GSX, Los Polvorines, Buenos Aires, Argentina
[5] Univ Nacl Litoral, Fac Ingn Quim, Santiago Estero 2829, RA-3000 Santa Fe, Argentina
关键词
CO oxidation; Gold; Iridium; Ceria; DRIFT; Modulation excitation spectroscopy; CARBON-MONOXIDE OXIDATION; GAS SHIFT CATALYSTS; PREFERENTIAL OXIDATION; DEPOSITION-PRECIPITATION; DOPED CERIA; VIBRATIONAL SPECTROSCOPY; METAL-CATALYSTS; AU CATALYSTS; TEMPERATURE; IR;
D O I
10.1007/s11244-019-01185-y
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Monometallic gold and iridium, and bimetallic gold-iridium on ceria-niobia (Nb2O5-CeO2) catalysts were synthesized by deposition-precipitation with urea. Ceria-niobia support, synthesized by co-precipitation, presented a higher reducibility and a higher surface acidity as a consequence of the deposition of niobia on the ceria surface. The Au-Ir/CeNb showed an enhanced activity and stability during the carbon monoxide oxidation reaction as compared with the monometallic catalysts. These catalysts were thoroughly characterized chemical and structurally. High-resolution electron microscopy, UV-Vis spectroscopy and CO adsorption showed evidences of iridium-gold closeness. In situ infrared spectroscopy in the diffuse reflectance (DRIFT) mode was used to investigate the reactivity of the active sites. A lower coverage of carbonate species was observed under reaction as a result of the presence of niobia in the catalyst formulation. Concentration-modulation excitation spectroscopy (c-MES) allowed a selective identification of intermediates and 'spectator' species. New adsorption sites for CO were identified and correlated with the high activity and stability of the bimetallic catalyst.
引用
收藏
页码:977 / 988
页数:12
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