Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/91830
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dc.titleThermal evolution of cobalt hydroxides: A comparative study of their various structural phases
dc.contributor.authorXu, Z.P.
dc.contributor.authorZeng, H.C.
dc.date.accessioned2014-10-09T08:22:47Z
dc.date.available2014-10-09T08:22:47Z
dc.date.issued1998-11
dc.identifier.citationXu, Z.P.,Zeng, H.C. (1998-11). Thermal evolution of cobalt hydroxides: A comparative study of their various structural phases. Journal of Materials Chemistry 8 (11) : 2499-2506. ScholarBank@NUS Repository.
dc.identifier.issn09599428
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/91830
dc.description.abstractThrough an atmosphere-controlled method, a new phase of hydrotalcite-like Co hydroxide with mixed valent states has been synthesised, along with preparations of known α and β phases. Structural and thermal behaviours of all the Co hydroxides have been compared. Three major stages of decomposition are found: (i) 149-164°C for dehydration of interlayer water, (ii) 185-197°C and (iii) 219-222°C for dehydroxylation of hydrotalcite- and brucite-like phases, respectively. Intercalated nitrate anions in hydrotalcite-like phases decompose largely during stage (ii). The oxide Co3O4 starts to form at temperatures as low as 165°C especially for hydrotalcite-like phases. An intermediate compound, HCoO2, which is formed thermally, decomposes at 258-270°C. The Co3O4 oxide converts into CoO at 842-858 and 935-948°C respectively in nitrogen and air, which is much lower than the previously reported range of 1000-1200°C. Surface areas of calcined samples are found to be proportional to the intercalated anion content. The catalytic activity of the resultant Co3O4 oxides with nitrous oxide is 7.2-8.2 mmol N2O g-1 h-1 at 375°C, which is comparable to some reported active catalyst systems.
dc.sourceScopus
dc.typeReview
dc.contributor.departmentCHEMICAL ENGINEERING
dc.description.sourcetitleJournal of Materials Chemistry
dc.description.volume8
dc.description.issue11
dc.description.page2499-2506
dc.description.codenJMACE
dc.identifier.isiutNOT_IN_WOS
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