Supported CuO plus Ag/partially stabilized zirconia catalysts for the selective catalytic reduction of NOx under lean burn conditions - 1. Bulk and surface properties of the catalysts

Citation
Va. Sadykov et al., Supported CuO plus Ag/partially stabilized zirconia catalysts for the selective catalytic reduction of NOx under lean burn conditions - 1. Bulk and surface properties of the catalysts, J CATALYSIS, 200(1), 2001, pp. 117-130
Citations number
24
Categorie Soggetti
Physical Chemistry/Chemical Physics","Chemical Engineering
Journal title
JOURNAL OF CATALYSIS
ISSN journal
00219517 → ACNP
Volume
200
Issue
1
Year of publication
2001
Pages
117 - 130
Database
ISI
SICI code
0021-9517(20010515)200:1<117:SCPASZ>2.0.ZU;2-O
Abstract
Thermally stable cubic mesoporous zirconia samples stabilized by the alkali ne-earth cations (Ca, Sr, Pa) were synthesized via the coprecipitation rout e followed by refluxing in the presence of surfactants. These systems were used as supports for copper cations and then modified by the addition of si lver nanoparticles using impregnation or photoassisted deposition technique s. The structural, textural, and surface features of these nanosystems were studied by using TEM, X-ray diffraction, EXAFS, nitrogen adsorption isothe rms, SAXS, FTIRS of adsorbed CO, and TPD of adsorbed NOx species. Partially stabilized zirconia samples were found to possess a disordered cubic struc ture. A higher tendency of bulky Pa cation to segregate in the surface laye r is reflected in a higher degree of surface disordering, higher concentrat ion of hydroxyls, and greater coordination unsaturation of isolated copper cations. In contrast to such traditional supports as gamma -alumina, stabil ized zirconia supports appear to favor formation of small reactive (probabl y, three-dimensional) clusters of copper cations possessing an increased re activity and decreased strength of oxygen bonding with these cations. It is reflected in decreased thermal stability of surface nitrite and nitrate sp ecies located at these centers as compared with such species on the surface of CuO/alumina catalysts. This feature seems to be primarily determined by the specificity of the surface structure of fluorite-like supports (ceria, zirconia). Silver incorporation into copper oxidic clusters decreases the strength of copper-oxygen bonds as well as the thermal stability of adsorbe d nitrite-nitrate species. For samples prepared via the photodeposition rou te, the clustering degree of copper cations is usually lower than in the ca se of samples obtained by traditional impregnation procedure. (C) 2001 Acad emic Press.