Catalytic processes during preferential oxidation of CO in H2-rich streams over catalysts based on copper-ceria

被引:108
作者
Gamarra, D.
Hornes, A.
Koppany, Zs.
Schay, Z.
Munuera, G.
Soria, J.
Martinez-Arias, A.
机构
[1] CSIC, Inst Catalisis & Petroleoquim, Madrid 28049, Spain
[2] Hungarian Acad Sci, Inst Isotopes, H-1525 Budapest, Hungary
[3] CISC, Dept Quim Inorgan, Seville 41092, Spain
[4] CISC, Inst Ciencia Mat, Seville 41092, Spain
关键词
CuO/CeO2; CO-PROX; H-2-TPR; CO-TPR; XPS; microemulsion;
D O I
10.1016/j.jpowsour.2007.01.048
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
Nanostructured catalysts based on combinations between oxidised copper and cerium entities prepared by two different methods (impregnation of ceria and coprecipitation of the two components within reverse microemulsions) have been examined with respect to their catalytic performance for preferential oxidation of CO in a H-2-rich stream (CO-PROX). Correlations between their catalytic and redox properties are established on the basis of parallel analyses of temperature programmed reduction results employing both H-2 and CO as reactants as well as by XPS. Although general catalytic trends can be directly correlated with the redox properties observed upon separate interactions with each of the two reductants (CO and H-2), the existence of interferences between both reductants must be considered to complete details for such activity/redox correlation. Differences in the nature of the active oxidised copper-cerium contacts present in each case determine the catalytic properties of these systems for the CO-PROX process. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:110 / 116
页数:7
相关论文
共 40 条
[1]   Influence of the preparation method on the performance of CuO-CeO2 catalysts for the selective oxidation of CO [J].
Avgouropoulos, G ;
Ioannides, T ;
Matralis, H .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2005, 56 (1-2) :87-93
[2]   A comparative study of Pt/γ-Al2O3, Au/α-Fe2O3 and CuO-CeO2 catalysts for the selective oxidation of carbon monoxide in excess hydrogen [J].
Avgouropoulos, G ;
Ioannides, T ;
Papadopoulou, C ;
Batista, J ;
Hocevar, S ;
Matralis, HK .
CATALYSIS TODAY, 2002, 75 (1-4) :157-167
[3]   Structural investigation of combustion synthesized Cu/CeO2 catalysts by EXAFS and other physical techniques:: Formation of a Ce1-xCuxO2-δ solid solution [J].
Bera, P ;
Priolkar, KR ;
Sarode, PR ;
Hegde, MS ;
Emura, S ;
Kumashiro, R ;
Lalla, NP .
CHEMISTRY OF MATERIALS, 2002, 14 (08) :3591-3601
[4]   Active nonmetallic Au and Pt species on ceria-based water-gas shift catalysts [J].
Fu, Q ;
Saltsburg, H ;
Flytzani-Stephanopoulos, M .
SCIENCE, 2003, 301 (5635) :935-938
[5]  
GAMARRA D, UNPUB J CATAL
[6]  
GAMARRA D, IN PRESS
[7]  
GRUNERT W, 1994, J PHYS CHEM-US, V98, P10832
[8]   Peak shape analysis of core level photoelectron spectra using UNIFIT for WINDOWS [J].
Hesse, R ;
Chassé, T ;
Szargan, R .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1999, 365 (1-3) :48-54
[9]  
Holgado JP, 1995, STUD SURF SCI CATAL, V96, P109
[10]   Study of CeO2 XPS spectra by factor analysis:: reduction of CeO2 [J].
Holgado, JP ;
Alvarez, R ;
Munuera, G .
APPLIED SURFACE SCIENCE, 2000, 161 (3-4) :301-315