A CO-TAP study of the reducibility of La1-xSrxFe(Pd)O3±δ perovskites

被引:16
作者
Song, Zhaoxia [1 ]
Nishiguchi, Hiroyasu [1 ]
Liu, Wei [1 ]
机构
[1] Oita Univ, Fac Engn, Dept Appl Chem, Oita 8701192, Japan
关键词
temporal analysis of products (TAP); perovskite; reducibility; sol-gel auto-combustion method;
D O I
10.1016/j.apcata.2006.03.048
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
In order to obtain useful information about the effect of Sr, Pd promotion and calcination temperature on the reducibility of La(1-x)SrFc(Pd)O-3 +/-delta perovskites, CO-TAP in combination with XRD, BET, TG-DTA, and SEM were employed to characterise the perovskite oxides prepared by the method of sol-gel auto-combustion. Reducibility of the perovskites was studied by means of the oxygen release capacity measurement in which a TAP reactor system was used to perform the CO pulse or alternate CO-O-2 pulse experiments. Partial substitution of La3+ by Sr2+ in LaFeO3 significantly enhanced the reducibility and La0.6Sr0.4FeO3 +/-delta showed the highest reducibility among the La1-xSxFeO3 +/-delta perovskites. An incorporation of I'd in replacement of 5 mol% of Fe into La0.6Sr0.4FeO3 +/-delta caused a significant decrease of reduction temperature and an enhancement of reducibility. Moreover, the thermal stability was improved in the presence of Pd. It was found that the reducibility was strongly affected by the calcination temperatures. Extremely high reducibility (ca. 650 mu mol-CO2 g(-1) of OSC and ca. 800 mu mol-CO2 g(-1) of OSCC) was observed on the 1000 degrees C calcined La0.6Sr0.4Fe0.95Pd0.05O3 +/-delta although its BET specific surface area was very low. We concluded that calcination of La0.6Sr0.4Fe0.95Pd0.05O3 +/-delta at relatively high temperatures was favourable of creating more lattice defects and the lattice defects instead of surface area were mainly responsible for the reducibility. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:175 / 183
页数:9
相关论文
共 37 条
[1]   Investigation of the oxygen storage process on ceria- and ceria-zirconia-supported catalysts [J].
Bedrane, S ;
Descorme, C ;
Duprez, D .
CATALYSIS TODAY, 2002, 75 (1-4) :401-405
[2]   On the mechanism of fast oxygen storage and release in ceria-zirconia model catalysts [J].
Boaro, M ;
Giordano, F ;
Recchia, S ;
Dal Santo, V ;
Giona, M ;
Trovarelli, A .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2004, 52 (03) :225-237
[3]   The dynamics of oxygen storage in ceria-zirconia model catalysts measured by CO oxidation under stationary and cycling feedstream compositions [J].
Boaro, M ;
de Leitenburg, C ;
Dolcetti, G ;
Trovarelli, A .
JOURNAL OF CATALYSIS, 2000, 193 (02) :338-347
[4]   RUTHENIUM PEROVSKITE CATALYSTS FOR LEAN NOX AUTOMOTIVE EMISSION CONTROL [J].
BRADOW, R ;
JOVANOVIC, D ;
PETROVIC, S ;
JOVANOVIC, Z ;
TERLECKIBARICEVIC, A .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1995, 34 (06) :1929-1932
[5]  
CAMPAGNOLI E, 2004, APPL CATAL B-ENVIRON, V55, P127
[6]   Novel oxygen storage components for advanced catalysts for emission control in natural gas fueled vehicles [J].
Chang, YF ;
McCarty, JG .
CATALYSIS TODAY, 1996, 30 (1-3) :163-170
[7]   Thermochemistry of La1-xSrxFeO3-δ solid solutions (0.0 ≤ x ≤ 1.0, 0.0 ≤ δ ≤ 0.5) [J].
Cheng, JJ ;
Navrotsky, A ;
Zhou, XD ;
Anderson, HU .
CHEMISTRY OF MATERIALS, 2005, 17 (08) :2197-2207
[8]   Combustion synthesis of perovskite-type catalysts for natural gas combustion [J].
Civera, A ;
Pavese, M ;
Saracco, G ;
Specchia, V .
CATALYSIS TODAY, 2003, 83 (1-4) :199-211
[9]   Perovskite-type halo-oxide La1-xSrxFeO3-δXσ (X=F, Cl) catalysts selective for the oxidation of ethane to ethene [J].
Dai, HX ;
Ng, CF ;
Au, CT .
JOURNAL OF CATALYSIS, 2000, 189 (01) :52-62
[10]   Oxygen storage capacity measurements of three-way catalysts under transient conditions [J].
Descorme, C ;
Taha, R ;
Mouaddib-Moral, N ;
Duprez, D .
APPLIED CATALYSIS A-GENERAL, 2002, 223 (1-2) :287-299