Thermal decomposition of Manganese(II) oxalate in vacuum and in oxygen

Authors:
  • MBMichael E. Brown
    Michael E. Brown
  • DDDavid Dollimore
    David Dollimore
  • AGAndrew K. Galwey
    Andrew K. Galwey
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Abstract
Comparative studies of the kinetics of thermal decomposition of anhydrous manganese(II) oxalate in vacuum and in oxygen are reported. Reaction rates were appreciably influenced by the conditions of salt dehydration: both decompositions were more rapid for vacuum-dehydrated reactant than for salt dehydrated in air. The shapes of product yield against time curves were not detectably changed by the presence of oxygen. The solid product from the oxidation reaction was largely Mn2O3 and the activation energy was significantly lower than previously reported values for the vacuum decomposition which yields MnO. Mechanistic interpretation of the kinetic data was supplemented where appropriate by observations from electron micrographs. Product gas analyses, during the course of decomposition reactions, indicated the initial formation of products containing Mn3+, though this was subsequently reduced. Reaction mechanisms involving the participation of Mn3+ in both decomposition and oxidation of manganese(II) oxalate are proposed.