Gold nanoparticles:: Support effects for the WGS reaction

被引:120
作者
Sandoval, Alberto
Gomez-Cortes, Antonio
Zanella, Rodolfo
Diaz, Gabriela
Saniger, Jose M.
机构
[1] Univ Nacl Autonoma Mexico, Ctr Ciencias Aplicadas & Desarrollo Tecnol, Mexico City 04510, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Inst Fis, Mexico City 01000, DF, Mexico
关键词
gold; water gas shift; support reducibility; catalysts pretreatment; CO adsorption;
D O I
10.1016/j.molcata.2007.09.014
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Gold nanoparticles supported on reducible (TiO2 and CeO2) and non-reducible oxides (Al2O3 and SiO2) with comparable gold particle size (2.5-3.5 nm) were studied as catalysts in the WGS reaction. Deposition-precipitation with urea (DP Urea) was used to prepare gold nanoparticles supported on TiO2. CeO2, and Al2O3. Cationic adsorption was used as preparation method in the case of SiO2. Metal loading was fixed to 4 and 8 wt. %. The WGS reaction was studied in the temperature range from 50 to 400 degrees C in a flow reactor at atmospheric pressure. Before reaction the samples were calcined at 200, 300 or 400 degrees C to study the effect of calcination temperature in the catalyst activity. The Au/CeO2 catalyst showed an enhanced reduction at low-temperatures as evidenced by the H/Au ratio. The lowest reduction temperature was observed for gold in the Au/TiO2, catalyst. When supported on TiO2, and CeO2, the activity of gold nanoparticles was much higher than the one observed when supported on Al2O3 and SiO2, being the Au/SiO2, catalyst practically inactive. For samples calcined at 300 degrees C and reaction temperatures below 225 degrees C the activity varied as follows: TiO2 > CeO2 >> Al2O3. CO adsorption in the presence of H2O was followed by DRIFT. Bands coming from C-H stretching associated to formate species were clearly observed on CeO,. Intensity of these bands decreased when Au is present on the supports. Au-0-CO adsorption band was evidenced when Au is supported on TiO2, CeO2 and Al2O3. Fast conversion of formate species in Au/TiO2 and Au/CeO2 takes place and this explains the higher activity displayed by these catalysts. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:200 / 208
页数:9
相关论文
共 53 条
[1]   Au/α-Fe2O3 catalyst for water-gas shift reaction prepared by deposition-precipitation [J].
Andreeva, D ;
Tabakova, T ;
Idakiev, V ;
Christov, P ;
Giovanoli, R .
APPLIED CATALYSIS A-GENERAL, 1998, 169 (01) :9-14
[2]   Low-temperature water-gas shift reaction on Au/alpha-Fe2O3 catalyst [J].
Andreeva, D ;
Idakiev, V ;
Tabakova, T ;
Andreev, A ;
Giovanoli, R .
APPLIED CATALYSIS A-GENERAL, 1996, 134 (02) :275-283
[3]   Low-temperature water-gas shift reaction over Au/CeO2 catalysts [J].
Andreeva, D ;
Idakiev, V ;
Tabakova, T ;
Ilieva, L ;
Falaras, P ;
Bourlinos, A ;
Travlos, A .
CATALYSIS TODAY, 2002, 72 (1-2) :51-57
[4]   Nanosize gold catalysts promoted by vanadium oxide supported on titania and zirconia for complete benzene oxidation [J].
Andreeva, D ;
Tabakova, T ;
Ilieva, L ;
Naydenov, A ;
Mehanjiev, D ;
Abrashev, MV .
APPLIED CATALYSIS A-GENERAL, 2001, 209 (1-2) :291-300
[5]  
[Anonymous], 1984, INFRARED SPECTROSCOP
[6]   Selective CO oxidation in a hydrogen-rich stream over Au/γ-Al2O3 catalysts [J].
Bethke, GK ;
Kung, HH .
APPLIED CATALYSIS A-GENERAL, 2000, 194 :43-53
[7]   THE REACTION OF GOLD(III) WITH SOME BIDENTATE COORDINATING GROUPS [J].
BLOCK, BP ;
BAILAR, JC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (10) :4722-4725
[8]   Gold, silver and copper catalysts supported on TiO2 for pure hydrogen production [J].
Boccuzzi, F ;
Chiorino, A ;
Manzoli, M ;
Andreeva, D ;
Tabakova, T ;
Ilieva, L ;
Iadakiev, V .
CATALYSIS TODAY, 2002, 75 (1-4) :169-175
[9]   FTIR study of the low-temperature water-gas shift reaction on Au/Fe2O3 and Au/TiO2 catalysts [J].
Boccuzzi, F ;
Chiorino, A ;
Manzoli, M ;
Andreeva, D ;
Tabakova, T .
JOURNAL OF CATALYSIS, 1999, 188 (01) :176-185
[10]   FTIR study of carbon monoxide oxidation and scrambling at room temperature over gold supported on ZnO and TiO2 .2. [J].
Boccuzzi, F ;
Chiorino, A ;
Tsubota, S ;
Haruta, M .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (09) :3625-3631