Partial oxidation of methane to synthesis gas over Ru/TiO2 catalysts: Effects of modification of the support on oxidation state and catalytic performance

Citation
C. Elmasides et al., Partial oxidation of methane to synthesis gas over Ru/TiO2 catalysts: Effects of modification of the support on oxidation state and catalytic performance, J CATALYSIS, 198(2), 2001, pp. 195-207
Citations number
49
Categorie Soggetti
Physical Chemistry/Chemical Physics","Chemical Engineering
Journal title
JOURNAL OF CATALYSIS
ISSN journal
00219517 → ACNP
Volume
198
Issue
2
Year of publication
2001
Pages
195 - 207
Database
ISI
SICI code
0021-9517(20010310)198:2<195:POOMTS>2.0.ZU;2-0
Abstract
The effects of modification of the support on the oxidation state of Ru and the catalytic performance of Ru/TiO2 catalysts under conditions of partial oxidation of methane to synthesis gas have been investigated employing XPS and FTIR techniques. It has been found that the oxidation state of Ru depe nds on the reaction temperature and on the supporting material and that, un der conditions where the direct reaction route is operable, the catalytic p erformance (conversion of methane and selectivity toward synthesis gas form ation) is improved over samples that mainly contain Ru in its metallic form . Doping of TiO2 with small amounts of W6+ cations favors oxygen adsorption on Ru under reaction conditions, thus resulting in stabilization of a frac tion of the catalyst in its oxide forms. This is reflected in lower activit y and selectivity of this catalyst compared to those of the undoped one. In contrast, Ru supported on undoped and Ca2+-doped TiO2 exists mainly in the metallic form and, as a result, it promotes the direct conversion of metha ne to synthesis gas. In situ FTIR spectroscopy showed that an adsorbed CO s pecies exists on the surface of the latter two catalysts under reaction con ditions, even at temperatures as high as 1073 K. This species, which is not observable over the W6+-doped catalyst, is related to a Ru surface site, w hich is responsible for the dissociation of methane rind formation of CO. ( C) 2001 Academic Press.