A simple flow-system was designed to study the dissolution of cobaltous oxide (CoO) at surface conditions (25° and 39°C, one atmosphere). Experiments were carried out using solutions with salinities less than 0.01
m and pH's of 0.7-3.46. The dissolution was found to be controlled by surface reactions and has a reaction order of 0.67±0.05 with respect to hydrogen ion concentration. The integrated kinetic equation has the form [Co(H
2O)
62+] =k
+/k
- [H
+]
0.67(1-e
-Ak_t) where k
+ and k
- are reaction rates for the forward and reverse reactions, and were determined to be 1.05±0.26×10
-10 m
-2s
-1 and 7.25±1.20×10
-10 m
-2s
-1 respectively. CoO is not stable in acidic aqueous solutions under surface conditions. It gradually transforms into cobalt spinel (Co
3O
4) and which is effectively insoluble under our experimental conditions. A rate constant of 0.0038 day
-1 was estimated for the phase transition reaction (CoO→Co
3O
4) assuming a first-order reaction model.
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