THERMAL REVOLUTION OF COBALT HYDROXIDES - A COMPARATIVE-STUDY OF THEIR VARIOUS STRUCTURAL PHASES

Authors
Citation
Zp. Xu et Hc. Zeng, THERMAL REVOLUTION OF COBALT HYDROXIDES - A COMPARATIVE-STUDY OF THEIR VARIOUS STRUCTURAL PHASES, Journal of materials chemistry (Print), 8(11), 1998, pp. 2499-2506
Citations number
34
Categorie Soggetti
Chemistry Physical","Material Science
ISSN journal
09599428
Volume
8
Issue
11
Year of publication
1998
Pages
2499 - 2506
Database
ISI
SICI code
0959-9428(1998)8:11<2499:TROCH->2.0.ZU;2-T
Abstract
Through an atmosphere-controlled method, a new phase of hydrotalcite-l ike Co hydroxide with mixed valent states has been synthesised, along with preparations of known alpha and beta phases. Structural and therm al behaviours of all the Co hydroxides have been compared. Three major stages of decomposition are found: (i) 149-164 degrees C for dehydrat ion of interlayer water, (ii) 185-197 degrees C and (iii) 219-222 degr ees C for dehydroxylation of hydrotalcite- and brucite-like phases, re spectively. Intercalated nitrate anions in hydrotalcite-like phases de compose largely during stage (ii). The oxide Co3O4 starts to form at t emperatures as low as 165 degrees C especially for hydrotalcite-like p hases. An intermediate compound, HCoO2, which is formed thermally, dec omposes at 258-270 degrees C. The Co3O4 oxide converts into CoO at 842 -858 and 935-948 degrees C respectively in nitrogen and air, which is much lower than the previously reported range of 1000-1200 degrees C. Surface areas of calcined samples are found to be proportional to the intercalated anion content. The catalytic activity of the resultant Co 3O4 oxides with nitrous oxide is 7.2-8.2 mmol N2O g(-1) h(-1) at 375 d egrees C, which is comparable to some reported active catalyst systems .