IP Library Granted Patent US 7,998,452
Granted Patent B2
US 7,998,452 · App. 12/614,611 · Granted Aug 16, 2011

Spherical tricobalt tetraoxide and method of preparing the same

Assignee: Ningbo Jinhe New Materials Co., Ltd.
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Quick Facts
Patent No.
US 7,998,452
App. No.
12/614,611
Granted
Aug 16, 2011
Kind
B2
Abstract

A method of preparation of spherical tricobalt tetraoxide, including at least oxidizing a bivalent cobalt salt in a wet environment and in the presence of a precipitant, a complexing agent, and an oxidant to yield spherical cobalt oxyhydroxide.cobalt hydroxide according to the following equation Co 2+ +3OH − +O→CoOOH.Co(OH) 2 ; oxidizing the spherical hydroxy cobalt oxyhydroxide.cobalt hydroxide to yield spherical tricobalt tetraoxide according to the following equation 6CoOOH.Co(OH) 2 +O→4Co 3 O 4 +9H 2 O; and roasting the spherical tricobalt tetraoxide at low or intermediate temperature to yield a black powder. The method is easily practiced and suitable for mass production, and the resultant spherical tricobalt tetraoxide has stable structure, reliable properties, and high activity.

Claims (12)

1. A method of preparation of tricobalt tetraoxide, comprising: (i) oxidizing a bivalent cobalt salt in a wet environment and in the presence of an oxidant, a base, and a complexing agent to yield cobalt oxyhydroxide.cobalt hydroxide; (ii) oxidizing the cobalt oxyhydroxide.cobalt hydroxide to yield tricobalt tetraoxide; and (iii) roasting the tricobalt tetraoxide to yield tricobalt tetraoxide.

2. The method of claim 1 , comprising the steps of:

a) preparing a cobalt salt solution having concentration of between 0.5 and 3 mol/L;

b) preparing a base solution having concentration of between 1 and 10 mol/L as a precipitant solution;

c) preparing a complexing agent solution having concentration of between 0.5 and 200 g/L;

d) mixing said cobalt salt solution, said base solution, and said complexing agent solution in a reactor to form a reaction mixture, allowing the reaction mixture to react with stirring, and constantly adding an oxidant during the reaction; controlling the pH value of the reaction mixture at between 8 and 13, and controlling the reaction temperature at between 40 and 90° C.;

e) stirring the reaction mixture for between 2 and 48 hrs at a constant temperature; followed by centrifuging, washing, drying, and grinding to yield a precursor of spherical tricobalt tetraoxide; and

f) roasting said precursor for between 2 and 20 hrs at between 200 and 500° C. to yield spherical tricobalt tetraoxide in a powder form.

3. The method of claim 2 , wherein said oxidant is oxygen, air, or hydrogen peroxide, and said oxidant is added in a 1.2 to 3.0 times excess.

4. The method of claim 2 , wherein said cobalt salt is cobalt sulfate, cobalt chloride, cobalt oxalate, or cobalt nitrate.

5. The method of claim 2 , wherein said base is sodium hydroxide, potassium hydroxide, or a mixture thereof.

6. The method of claim 2 , wherein said complexing agent is sodium tartrate, disodium EDTA, ethylenediamine, hexamethylenetetramine, polyacrylamide, or citric acid, or a mixture of two of these.

Assignments (3)
CHANGE OF NAME Recorded Apr 11, 2018
From: NINGBO JINHE LITHIUM BATTERY MATERIAL CO., LTD.
To: NINGBO RONBAY NEW ENERGY TECHNOLOGY CO., LTD.
Reel/Frame 045512/0327 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 4, 2014
From: NINGBO JINHE NEW MATERIALS CO., LTD.
To: NINGBO JINHE LITHIUM BATTERY MATERIAL CO., LTD.
Reel/Frame 034103/0706 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 9, 2009
From: HE, JINHUA
To: NINGBO JINHE NEW MATERIALS CO., LTD.
Reel/Frame 023489/0118 →
Priority Claims (1)
CN 2008 1 0162689 · Nov 28, 2008 · national
Continuity (1)
Related Publication 20100135897A1 · Jun 3, 2010