Reaktionsgleichung
[O-:1][Mn:2](=[O:5])(=[O:4])=[O:3].[K+:6].[O-:7][S:8]([O-:11])(=[O:10])=[O:9].[Mn+2:12]>>[O:1]=[Mn:2]=[O:3].[O-:5][Mn:2](=[O:4])(=[O:3])=[O:1].[K+:6].[O-:10][S:8]([O-:11])(=[O:9])=[O:7].[Mn+2:12].[OH2:1]Komponenten
Reaktionsbedingungen
- Temperatur
- 30 °C
Versuchsvorschrift
A laboratory scale amount of alpha form of MnO2 (“Alpha-MnO2”) was prepared as follows. It is noted that high volume production of Alpha-MnO2 can be accomplished using other industrial processes. 200 ml of 0.1 M KMnO4 and 200 ml of 0.15M MnSO4.H2O were prepared and individually heated to 30° C. The KMnO4 solution was placed in a beaker and stirred in an ultrasonic bath. The MnSO4 solution was added drop wise into the KMnO4 solution. A brown precipitate appeared. The precipitation continued until all of the MnSO4 solution was consumed. The beaker was taken out of the ultrasonic bath and was allowed to settle for 1 hour. The solution along with the precipitate was centrifuged at 9000 rpm for 2 minutes. After discarding the liquid, the precipitate was washed in deionized (“DI”) water and centrifuged again at 9000 rpm for 2 minutes. The precipitate was retrieved and dried under vacuum at 80° C. for 2 hours. Finally the resulting dried precipitate powder was annealed in air at 200° C. for 12 hours.
Aufarbeitung
- customThe precipitation
- customwas consumed
- waitThe solution along with the precipitate was centrifuged at 9000 rpm for 2 minutes
- washthe precipitate was washed in deionized (“DI”) water
- waitcentrifuged again at 9000 rpm for 2 minutes
- customdried under vacuum at 80° C. for 2 hours
- customFinally the resulting dried precipitate powder
- waitwas annealed in air at 200° C. for 12 hours
Quellen und Nachweise
- ORD-Eintrag
- ord-d61c9bb7ef52471c8bb579987fa24993
- Quelldatensatz
- uspto-grants-2016_05
- Patentnummer
- US09340436B2
Verknüpfte Notizen
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