Please use this identifier to cite or link to this item:
https://scholarbank.nus.edu.sg/handle/10635/91743
DC Field | Value | |
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dc.title | Synthesis and characterization of Mg-Co catalytic oxide materials for low-temperature N2O decomposition | |
dc.contributor.author | Qian, M. | |
dc.contributor.author | Zeng, H.C. | |
dc.date.accessioned | 2014-10-09T08:21:45Z | |
dc.date.available | 2014-10-09T08:21:45Z | |
dc.date.issued | 1997-03 | |
dc.identifier.citation | Qian, M.,Zeng, H.C. (1997-03). Synthesis and characterization of Mg-Co catalytic oxide materials for low-temperature N2O decomposition. Journal of Materials Chemistry 7 (3) : 493-499. ScholarBank@NUS Repository. | |
dc.identifier.issn | 09599428 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/91743 | |
dc.description.abstract | Binary metal Mg-Co oxide materials have been synthesized from Mg-Co hydroxide precursors by a coprecipitation-then-calcination method. The oxide system shows high catalytic activity for low-temperature decomposition of N2O (27 mol%). Using FTIR, XRD, SEM, EA, DSC, BET and GC techniques, the hydrothermal synthesis and chemistry of the double-metal hydroxides have been studied in detail. In anion exchange and XRD studies, a hydrotalcite-like phase is also found to be present in the hydroxides owing to a partial oxidation of Co2+ to Co3+ in air. The precursor subjected to hydrothermal treatment has a higher Mg content, higher crystallinity and is more stable compared to the one aged at room temperature. However, they all give amorphous Mg-Co oxides after calcination. The Mg-Co oxide prepared from the hydrothermally treated precursor has a higher surface area and is more active for N2O decomposition. With this material system, ca. 6 moles of N2O per kg of the precursor materials can be decomposed at 350°C within 1 h. | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMICAL ENGINEERING | |
dc.description.sourcetitle | Journal of Materials Chemistry | |
dc.description.volume | 7 | |
dc.description.issue | 3 | |
dc.description.page | 493-499 | |
dc.description.coden | JMACE | |
dc.identifier.isiut | NOT_IN_WOS | |
Appears in Collections: | Staff Publications |
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