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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Chen, Min | - |
| dc.contributor.author | Zheng, Xiao-Ming | - |
| dc.date.accessioned | 2013-05-28T09:31:44Z | - |
| dc.date.available | 2013-05-28T09:31:44Z | - |
| dc.date.issued | 2001-03 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/18471 | - |
| dc.description | 298-302 | en_US |
| dc.description.abstract | Ag-Fe mixed oxides catalysts with different Ag/Fe ratio are prepared by co-precipitation method. The catalysts have been characterized by X-ray diffraction (XRD). XRD shows that over all the catalysts exist as the σ-AgFeO2 phase. The surface oxygen species of catalysts and the reduction properties of catalysts have been investigated by temperature-programmed decomposition (TPD) and reduction (TPR). It has been found that only one peak is observed on O2- TPD profiles which is attributed to lattice oxygen from finely dispersed σ-AgFeO2 phases. Three reducible peaks (α, β,γ) have been observed on H2-TPR profiles. The α peak (around 180-220°C) is attributed to the reduction of the small phase of σ-AgFeO2, β peak (around 250-280°C) is attributed to the reduction of the large phase of σ-AgFeO2, and they peak is attributed to the reduction of Fe2O3 species. The results indicate that the Ag/Fe (1:1) catalyst exhibits highest oxidation activity in CO oxidation. It has been found that the σ-AgFeO2 phase is the active site which makes main contribution in CO oxidation reaction. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights | CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-A Vol.40A(03) [March 2001] | en_US |
| dc.title | Catalyst characterization and surface oxygen properties of Ag-Fe mixed oxide catalysts | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.40A(03) [March 2001] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 40A(3) 298-302.pdf | 1.01 MB | Adobe PDF | View/Open |
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