Sodium Hydroxide → Nickel-cobalt-manganese hydroxide

HRID 131065

反応式

HRID 131065 の反応式
S([O-])([O-])(=O)=[O:2].[Ni+2:6].S([O-])([O-])(=O)=[O:8].[Mn+2:12].S([O-])([O-])(=O)=[O:14].[Co+2:18].S([O-])([O-])(=O)=[O:20].[NH4+].[NH4+].[OH-:26].[Na+]>>[OH-:2].[Co+2:18].[Mn+2:12].[Ni+2:6].[OH-:8].[OH-:14].[OH-:20].[OH-:26].[OH-:2]

参加物

6

反応条件

温度
50 °C

実験手順

In a 2-L (liter) reaction vessel, 1.8 L of the mother liquor obtained in the above-described Example 1 was poured, and agitated at 250 rpm while maintaining the internal temperature at 50±1° C. To this, while supplying an aqueous solution of metal sulfates containing 1.5 mol/L of nickel sulfate, 1.5 mol/L of manganese sulfate and 1.5 mol/L of cobalt sulfate at a flow rate of 0.4 L/hr; and simultaneously supplying a 1.5 mol/L aqueous solution of ammonium sulfate at a flow rate of 0.03 L/hr; an 18 mol/L aqueous solution of sodium hydroxide was continuously supplied so that the pH in the reaction vessel was maintained at 11.05±0.05. The mother liquor in the reaction vessel was periodically extracted, and the slurry was concentrated until the final slurry concentration became about 1000 g/L. The nickel concentration in the periodically extracted mother liquor from the reaction vessel was 22 ppm. After the target slurry concentration had been obtained, the slurry was aged at 50° C. for 5 hours, filtration and water washing were repeated to obtain coagulated particles of a co-precipitated nickel-manganese-cobalt hydroxide.

後処理

  1. customobtained in the above-described Example 1
  2. additionwas poured
  3. temperaturewas maintained at 11.05±0.05
  4. extractionThe mother liquor in the reaction vessel was periodically extracted
  5. concentrationthe slurry was concentrated until the final
  6. concentrationslurry concentration
  7. concentrationThe nickel concentration in the periodically extracted mother liquor from the reaction vessel
  8. concentrationAfter the target slurry concentration
  9. customhad been obtained
  10. filtrationfiltration and water washing

出典と根拠

ORDレコード
ord-1bdfd983426b4bb9b1c6993dca6f8b5c
出典データセット
uspto-grants-2008_06
特許番号
US07384706B2

関連ノート

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