The coagulation reaction of chromium ion was investigated by means of distribution curves of chromium (III) aquacomplexes in Cr
2(SO
4)
3 solution and titration curves, solubility curves, and sedimentation volume in binary systems such as Cr
3+-Fe
3+, Cr
3+-Fe
2+, Cr
3+-Cu
2+, Cr
3+-Zn
2+, and Cr
3+-Ni
2+. The chromium ion was found to form aquacomplexes having positive or negative charge in aqueous solution by means of ion-exchange method. The positively charged aquacomplexes in the solution amounted to 70% of total complexes before titration with an alkali; but they decreased to 50% in the pH range for precipitation. Therefore, it would mainly be positively charged aquacomplexes which were precipitated in the earlier stage of coagulation reaction. In binary systems of Cr
3+-Fe
3+ and Cr
3+-Cu
2+ systems, the aspect of precipitation of each ion was distinguishable in the titration curves and solubility curves; but in Cr
3+-Fe
2+, Cr
3+-Zn
2+, and Cr
3+-Ni
2+ systems, the forms or those curves were nearly identical with those in chromium solution. Furthermore, as the results of sedimentation volume, the precipitate of Cr
3+-Cu
2+ system was considered to be nearly the mixture of individual precipitates, but the precipitate of Cr
3+-Zn
2+ system was not considered to be the mixture. Therefore, in binary systems, Fe
2+, Zn
2+, and Ni
2+ would co-precipitate with chromium ion, but the co-precipitation of Fe
3+ and Cu
2+ with chromium ion would be very little.
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