Surface interaction and reaction of NO plus CO on a supported Au catalyst

被引:50
作者
Solymosi, F
Bánsági, T
Zakar, TS
机构
[1] Univ Szeged, Inst Solid State & Radiochem, H-6701 Szeged, Hungary
[2] Hungarian Acad Sci, React Kinet Res Grp, H-6701 Szeged, Hungary
关键词
D O I
10.1039/b305427f
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 adsorption, dissociation and reaction of NO with CO have been investigated on supported Au catalysts. The main method was FTIR spectroscopy. Although very limited dissociation of NO was observed on reduced Au catalyst, catalytic tests showed that all the samples used effectively catalyse the NO + CO reaction above 573 K. By means of FTIR spectroscopy several new absorption bands have been detected on the Au samples, the position of which depended on the nature of the support: it was 2212 cm(-1) for Au/TiO2; 2220-2230 cm(-1) for Au/MgO; 2256 cm(-1) for Au/Al2O3; and 2305 cm(-1) for Au/ SiO2. These bands were attributed to the asymmetric stretch of NCO attached to the oxides. This idea was strengthened by the results obtained following the HNCO adsorption on supports alone, which gave the same absorption bands. It was demonstrated and assumed that an NCO species is formed on Au crystallites, and then migrates from the Au onto the acceptor sites of the support where it is accumulated and stabilized. The Au-NCO species was characterized by an absorption band at 2185-2195 cm(-1) produced either by the low temperature reaction or by the adsorption of HNCO on Au/SiO2.
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收藏
页码:4724 / 4730
页数:7
相关论文
共 47 条
[1]   INFRARED STUDY OF NITRIC-OXIDE ADSORBED ON RHODIUM-ALUMINA CATALYST [J].
ARAI, H ;
TOMINAGA, H .
JOURNAL OF CATALYSIS, 1976, 43 (1-3) :131-142
[2]  
Bansagi T., 1983, P INT S SPILL ADS SP, P109
[3]   FTIR study of CO oxidation on Au/TiO2 at 90 K and room temperature.: An insight into the nature of the reaction centers [J].
Boccuzzi, F ;
Chiorino, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (23) :5414-5416
[4]   Au/TiO2 nanosized samples:: A catalytic, TEM, and FTIR study of the effect of calcination temperature on the CO oxidation [J].
Boccuzzi, F ;
Chiorino, A ;
Manzoli, M ;
Lu, P ;
Akita, T ;
Ichikawa, S ;
Haruta, M .
JOURNAL OF CATALYSIS, 2001, 202 (02) :256-267
[5]   FTIR study of the electronic effects of CO adsorbed on gold nanoparticles supported on titania [J].
Boccuzzi, F ;
Chiorino, A ;
Manzoli, M .
SURFACE SCIENCE, 2000, 454 (01) :942-946
[6]   Catalysis by gold [J].
Bond, GC ;
Thompson, DT .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1999, 41 (3-4) :319-388
[7]   INFRARED STUDY OF INTERACTION BETWEEN ADSORBED CO AND ADSORBED NO ON SUPPORTED RU AND SUPPORTED PT [J].
BROWN, MF ;
GONZALEZ, RD .
JOURNAL OF CATALYSIS, 1976, 44 (03) :477-487
[8]   IR STUDY OF REACTIONS BETWEEN NO AND CO AND NO AND H-2 ON A SILICA-SUPPORTED RU CATALYST [J].
DAVYDOV, AA ;
BELL, AT .
JOURNAL OF CATALYSIS, 1977, 49 (03) :345-355
[9]   DRIFTS studies of the interaction of nitric oxide and carbon monoxide on Au-TiO2 [J].
Debeila, MA ;
Coville, NJ ;
Scurrell, MS ;
Hearne, GR .
CATALYSIS TODAY, 2002, 72 (1-2) :79-87