THERMAL-DECOMPOSITION OF POTASSIUM CHLORATE IN THE PRESENCE OF CHROMIUM(III) OXIDE

Authors
Citation
Sa. Halawy, THERMAL-DECOMPOSITION OF POTASSIUM CHLORATE IN THE PRESENCE OF CHROMIUM(III) OXIDE, Journal of analytical and applied pyrolysis, 28(2), 1994, pp. 219-229
Citations number
23
Categorie Soggetti
Spectroscopy,"Chemistry Analytical
ISSN journal
01652370
Volume
28
Issue
2
Year of publication
1994
Pages
219 - 229
Database
ISI
SICI code
0165-2370(1994)28:2<219:TOPCIT>2.0.ZU;2-Z
Abstract
The effect of the addition of chromium(III) oxide on the thermal decom position of potassium chlorate (PC) was studied using TG and DTG. Oxid e samples were prepared by calcination of Cr(NO3)3.9H2O and of chromia gel, as precursors, between 500 and 800-degrees-C. It was found that an oxide concentration of 10 wt.% by weight of PC was sufficiently act ive. Oxide activity was lowered as its calcination temperature was inc reased. Oxides prepared at 500-degrees-C from different precursors wer e characterized by X-ray powder diffraction to be Cr2O3. The DTA for P C showed one endotherm at 361-degrees-C due to fusion. This was follow ed by two exotherms at 426.8 and 442-degrees-C related to the decompos ition of PC and separation of KCl. DTA curves of the catalyzed decompo sition of PC exhibited a new exotherm at 415-degrees-C corresponding t o the formation of K2Cr2O7, followed by an endothermic peak at 420.7-4 36.2-degrees-C due to the melting of K2Cr2O7. IR spectroscopy confirme d the formation of K2Cr2O7 as a solid orange residue. The activation e nergies (DELTAE) of the thermal decomposition of pure PC and PC in the presence of Cr2O3 calcined at 500-degrees-C (from the different precu rsors) under non-isothermal conditions were calculated, from the TG re sults, using the Coats-Redfern equation. The decomposition process was found to obey the first order equation. A correlation between the oxi de precursors and their activities towards the decomposition of PC (DE LTAE values) was made through the calculated amount of excess surface oxygen for each oxide.