Silica supported ruthenium catalysts have been prepared by incipient wetness impregnation with RuCl3 (aq). After drying and reduction these catalysts were additionally treated with carbon monoxide or CO/H-2 at 250-degrees-C. Due to this treatment the catalyst's carbon monoxide chemisorption capacity significantly increased compared to normal reduction. At the same time the intrinsic reactivity for carbon monoxide dissociation is enhanced. These effects are attributed to the structural changes of the catalysts. A model, based on TPR, XPS, IR and TEM measurements, is proposed. The carbon monoxide treatment results in a catalyst that is better reducible and has larger metal ensembles.
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UNIV NEW S WALES,SCH CHEM IND & IND CHEM,POB 1,KENSINGTON,NSW 2033,AUSTRALIAUNIV NEW S WALES,SCH CHEM IND & IND CHEM,POB 1,KENSINGTON,NSW 2033,AUSTRALIA
CHEN, H
ADESINA, AA
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UNIV NEW S WALES,SCH CHEM IND & IND CHEM,POB 1,KENSINGTON,NSW 2033,AUSTRALIAUNIV NEW S WALES,SCH CHEM IND & IND CHEM,POB 1,KENSINGTON,NSW 2033,AUSTRALIA
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UNIV TOKYO, FAC ENGN, DEPT SYNTHET CHEM, HONGO, BUNKYO KU, TOKYO 113, JAPANUNIV TOKYO, FAC ENGN, DEPT SYNTHET CHEM, HONGO, BUNKYO KU, TOKYO 113, JAPAN
ENOMOTO, T
KATA, K
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UNIV TOKYO, FAC ENGN, DEPT SYNTHET CHEM, HONGO, BUNKYO KU, TOKYO 113, JAPANUNIV TOKYO, FAC ENGN, DEPT SYNTHET CHEM, HONGO, BUNKYO KU, TOKYO 113, JAPAN
KATA, K
OKUHARA, T
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UNIV TOKYO, FAC ENGN, DEPT SYNTHET CHEM, HONGO, BUNKYO KU, TOKYO 113, JAPANUNIV TOKYO, FAC ENGN, DEPT SYNTHET CHEM, HONGO, BUNKYO KU, TOKYO 113, JAPAN
OKUHARA, T
MISONO, M
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UNIV TOKYO, FAC ENGN, DEPT SYNTHET CHEM, HONGO, BUNKYO KU, TOKYO 113, JAPANUNIV TOKYO, FAC ENGN, DEPT SYNTHET CHEM, HONGO, BUNKYO KU, TOKYO 113, JAPAN