MoO3/ZrO2 and CrO3/ZrOn catalysts:: Study of the precursor formation

被引:9
作者
Cimino, A [1 ]
De Rossi, S [1 ]
Dragone, R [1 ]
Ferraris, G [1 ]
Gazzoli, D [1 ]
Valigi, M [1 ]
机构
[1] Univ La Sapienza, Dept Chem, Ctr Studio SACSO, I-00185 Roma, Italy
关键词
molybdena catalysts; chromia catalysts; zirconia; catalyst precursor formation; equilibrium adsorption;
D O I
10.1006/jcis.1997.5387
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
Equilibrium adsorption was used to study the influence of some parameters on the precursor formation of catalysts consisting of zirconia-supported chromia (ZC) or molybdena (ZMo). Uptake capacities of zirconia treated at various temperatures before adsorption (from 673 to 1023 K) showed little dependence on temperature. The Me uptake (Me = Cr or Mo) as a function of the equilibrium concentration of Me species in solution obeyed the Langmuir law for limited ranges. The Langmuir plots therefore yielded saturation coverage values, n(m), that depended on the concentration range. The meaning of "monolayer coverage" is discussed. The n(m) value measured at a range of solution pH from 1 to 8 depended little on pH. The values ranged from 1.6 to 2 atoms nm(-2) for Cr, and were around 3.6 atoms nm(-2) for Mo. The adsorption data suggested three adsorption regimes: (i) a strong, apparently irreversible adsorption, (ii) a partly reversible, direct adsorbate-surface interaction, corresponding to the initial stage in the Langmuir plots, which eventually merges in (iii), a weaker adsorption regime, showing an adsorbate-adsorbate interaction. We compare our data with reported values for Cr and Mo equilibrium adsorption on alumina. (C) 1998 Academic Press.
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页码:278 / 292
页数:15
相关论文
共 41 条
[1]  
Adamson A. W., 1990, PHYSICAL CHEM SURFAC, P421
[2]  
*ASTM, 1967, 7199 CARD ASTM
[3]   HETEROGENEITY OF V(2)O(5)/Al(2)O(3) AS STUDIED BY WATER VAPOUR ADSORPTION MICROCALORIMETRY [J].
Bailes, Michael ;
Stone, Frank S. .
CATALYSIS TODAY, 1991, 10 (03) :303-313
[4]   VANADIUM-OXIDE MONOLAYER CATALYSTS - PREPARATION, CHARACTERIZATION AND CATALYTIC ACTIVITY [J].
BOND, GC ;
TAHIR, SF .
APPLIED CATALYSIS, 1991, 71 (01) :1-31
[5]   Mechanisms of deposition of species containing catalytically active ions on the oxidic support electrolytic solution interfaces: A unified approach based on the two-pK/one-site and triple-layer models [J].
Bourikas, K ;
Matralis, HK ;
Kordulis, C ;
Lycourghiotis, A .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (28) :11711-11719
[6]   On a theory of the van der Waals adsorption of gases [J].
Brunauer, S ;
Deming, LS ;
Deming, WE ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1940, 62 :1723-1732
[7]  
BRUNAUER S, 1969, CHEM ENG PROG S SER, V65, P1
[8]  
BRUNELLE JP, 1979, PREPARATION CATALYST, V2, P211
[9]  
CHE M, 1993, NEW FRONTIERS CATALY, P32
[10]   STUDIES ON CHROMIA ZIRCONIA CATALYSTS .1. PREPARATION AND CHARACTERIZATION OF THE SYSTEM [J].
CIMINO, A ;
CORDISCHI, D ;
DEROSSI, S ;
FERRARIS, G ;
GAZZOLI, D ;
INDOVINA, V ;
MINELLI, G ;
OCCHIUZZI, M ;
VALIGI, M .
JOURNAL OF CATALYSIS, 1991, 127 (02) :744-760