Structural properties of Pd catalysts supported on Al2O3-La2O3 prepared by sol-gel method

被引:46
作者
Bogdanchikova, NE
Fuentes, S
Avalos-Borja, M
Farias, MH
Boronin, A
Diaz, G
机构
[1] Univ Nacl Autonoma Mexico, Ctr Ciencias Mat Condensada, Ensenada 22800, Baja California, Mexico
[2] CICESE, Ensenada, Baja California, Mexico
[3] Russian Acad Sci, Inst Catalysis, Novosibirsk 630090, Russia
[4] Univ Nacl Autonoma Mexico, Inst Fis, Mexico City, DF, Mexico
关键词
Pd/Al2O3-La2O3; catalysts; Sol-gel preparation method; XRD; HRTEM; XPS; NH3; production;
D O I
10.1016/S0926-3373(98)00010-1
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
The structure of palladium catalysts (0.3 wt% Pd), supported on sol-gel alumina-lanthana mixed oxides, was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM) and X-ray photoelectron spectroscopy (XPS), The investigation of the structure of lanthana-promoted Pd catalysts, prepared by different methods, is of great importance for the improvement of palladium-only three-way catalysts, The data obtained show the presence of a crystalline phase, different from alumina, lanthana or alumina-lanthana reported compounds, in Al2O3-La2O3 and Pd/Al2O3-La2O3. Attempts to assign this crystalline phase to a known one were unsuccessful. According to XPS data, in lanthanum-containing samples, the state of lanthanum is different from that in La2O3. After calcination in air at 1273 K for 3 h this phase vanishes and large crystals of LaAlO3, metastable for studied composition, appear. The sol-gel preparation method, in comparison with traditional preparation methods, leads to stabilization of LaAlO3 phase under the considered conditions and the increase of the stability of gamma-Al2O3 phase at high temperature. The improvement of the catalytic activity at medium temperature and the increase of the selectivity to NH3 at high temperatures for lanthanum-promoted Pd catalyst are ascribed to a lanthanum-containing phase. The increase in NH3 production decreases its practical value for an NO reduction catalyst. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:221 / 231
页数:11
相关论文
共 23 条
[11]  
MIZUKAMI F, 1991, STUD SURF SCI CATAL, V71, P557, DOI 10.1016/S0167-2991(08)63002-5
[12]  
MORRISS MA, 1996, P 11 INT C CAT 40 AN
[13]  
Moulder J.F., 1992, HDB XRAY PHOTOELECTR, P261, DOI DOI 10.1002/SIA.740030412
[14]   PALLADIUM LANTHANUM CATALYSTS FOR AUTOMOTIVE EMISSION CONTROL [J].
MURAKI, H ;
SHINJOH, H ;
SOBUKAWA, H ;
YOKOTA, K ;
FUJITANI, Y .
INDUSTRIAL & ENGINEERING CHEMISTRY PRODUCT RESEARCH AND DEVELOPMENT, 1986, 25 (02) :202-208
[15]   IDENTIFICATION OF THE STATE OF PALLADIUM IN VARIOUS HYDROGENATION CATALYSTS BY XPS [J].
NOACK, K ;
ZBINDEN, H ;
SCHLOGL, R .
CATALYSIS LETTERS, 1990, 4 (02) :145-156
[16]   ULTRAFINE ALUMINA POWDERS VIA A SOL EMULSION GEL METHOD [J].
PONTHIEU, E ;
PAYEN, E ;
GRIMBLOT, J .
JOURNAL OF NON-CRYSTALLINE SOLIDS, 1992, 147 :598-605
[17]  
Praliaud H, 1996, STUD SURF SCI CATAL, V101, P345
[18]   STUDIES OF THE INTERACTIONS OF H-2 AND CO WITH SILICA-SUPPORTED AND LANTHANA-SUPPORTED PALLADIUM [J].
RIECK, JS ;
BELL, AT .
JOURNAL OF CATALYSIS, 1985, 96 (01) :88-105
[19]   STUDIES OF THE INTERACTIONS OF H-2 AND CO WITH PD/SIO2 PROMOTED WITH LA2O3, CEO2, PR6O11, ND2O3, AND SM2O3 [J].
RIECK, JS ;
BELL, AT .
JOURNAL OF CATALYSIS, 1986, 99 (02) :278-292
[20]  
SATTERFIELD CN, 1983, HETEROGENEOUS CATALY, P416