The thermal decomposition of praseodymium oxalate decahydrate, Pr
2(C
2O
4)
3·10H
2O, was studied in atmospheres of He+O
2, He and CO
2 by a multiple technique of simultaneous thermogravimetry (TG) and differential thermal analysis (DTA) coupled with evolved gas analysis (EGA). The decomposition proceeded basically by the following steps in all the atmospheres:
Pr
2(C
2O
4)
3·10H
2O→Pr
2(C
2O
4)
3→Pr
2O(CO
3)
2→Pr
2O
2CO
3→Pr oxide,
yielding Pr
7O
12 in (4:1) He+O
2 mixture, and Pr
2O
3 in He and in CO
2 as end products. In CO
2 atmosphere, the decomposition of anhydrous oxalate took place at higher temperatures than in other atmospheres owing to the stabilization of intermediate carbonates. All the DTA peaks were endothermic in He and in CO
2, whereas exothermic peaks were also detected in He+O
2 probably due to the oxidation of CO and deposited carbon, and the disproportionation of CO. In inert atmospheres, finely divided carbon particles were markedly deposited, and then reacted with CO
2 which was evolved during the decomposition of Pr
2O
2CO
3. Instead of the disproportionation of CO, the direct formation of carbon and CO
2 from Pr
2O(CO
3)
2 was proposed as a possible mechanism for the deposition of carbon particles.
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