IP Library Granted Patent US 7,361,322
Granted Patent B2
US 7,361,322 · App. 11/673,352 · Granted Apr 22, 2008

Ceric oxide and method for production thereof, and catalyst for exhaust gas clarification

Assignee: Anan Kasei Co., Ltd.
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Quick Facts
Patent No.
US 7,361,322
App. No.
11/673,352
Granted
Apr 22, 2008
Kind
B2
Abstract

The present invention relates to ceric oxide that has excellent heat resistance and oxygen absorbing and desorbing capability useful as a co-catalyst material suitable for a catalyst for purifying exhaust gas, that is capable of maintaining a large specific surface area even in use in a high temperature environment, and that is suitable for use in a high temperature environment, yet capable of exhibiting high oxygen absorbing and desorbing capability also in a lower temperature range, a method for preparing such ceric oxide, and a catalyst for purifying exhaust gas utilizing such ceric oxide. The ceric oxide is an oxide composed essentially of ceric oxide, and has a specific surface area of not smaller than 30.0 m 2 /g after calcination at 900° C. for 5 hours.

Claims (18)

1. A ceric oxide which is an oxide consisting essentially of ceric oxide, and has following properties:

said ceric oxide has a specific surface area of not smaller than 30.0 m 2 /g after calcination at 900° C. for 5 hours, and

said ceric oxide has an S1/S2 ratio of not lower than 0.120 taken after calcination at 1000° C. for 5 hours, said S1/S2 ratio is a ratio of an area (S1) defined by a baseline and a TPR curve in a temperature range of 200 to 600° C. to an area (S2) defined by said baseline and said TPR curve in a temperature range of 600 to 1000° C.

2. The ceric oxide of claim 1 , wherein said ceric oxide has OSC of not smaller than 0.60 mlO 2 /g/s at 400° C., after calcination at 900° C. for 5 hours.

3. The ceric oxide of claim 1 , wherein said ceric oxide has a tap density of not higher than 1.3 g/ml, after calcination at 300° C. for 10 hours.

4. The ceric oxide of claim 1 , wherein said ceric oxide has a total pore volume of not smaller than 0.50 ml/g, after calcination at 300° C. for 10 hours.

5. A method for preparing a ceric oxide of claim 1 , comprising the steps of:

(a) providing a cerium solution wherein not less than 90 mol % of the cerium are tetravalent cerium ions, said cerium solution having a cerium concentration of 10 to 60 g/L in terms of cerium oxide;

(b) holding said cerium solution prepared in step (a) at 60 to 220° C. under heating;

(c) cooling said heated cerium solution;

(d) adding a precipitant to said cooled cerium solution to obtain a precipitate; and

(e) calcining said precipitate.

6. The method of claim 5 , wherein said calcining in step (e) is carried out at 250 to 900° C.

7. The method of claim 5 , further comprising, after step (d) and before step (e), step (d1) of heat-treating said precipitate obtained in step (d) in a solvent at 60 to 220° C. to obtain a precipitate.

8. The method of claim 5 , wherein said step (a) comprises:

(a-1) providing an initial cerium solution wherein not less than 90 mol % of the cerium are tetravalent cerium ions, and

(a-2) adjusting a cerium concentration of said initial cerium solution to prepare a cerium solution having a cerium concentration of 10 to 60 g/L in terms of cerium oxide.

9. A catalyst for purifying exhaust gas comprising a co-catalyst, wherein said co-catalyst comprises ceric oxide of claim 1 .

Assignments (3)
CHANGE OF NAME Recorded Mar 28, 2017
From: ANAN KASEI CO., LTD.
To: SOLVAY SPECIAL CHEM JAPAN, LTD.
Reel/Frame 042105/0311 →
CHANGE OF ADDRESS Recorded Mar 28, 2017
From: ANAN KASEI CO., LTD.
To: ANAN KASEI CO., LTD.
Reel/Frame 042105/0319 →
CHANGE OF ADDRESS Recorded Mar 3, 2008
From: ANAN KASEI CO., LTD.
To: ANAN KASEI CO., LTD.
Reel/Frame 020590/0702 →
Priority Claims (1)
JP 2001-272054 · Sep 7, 2001 · national
Continuity (2)
Continuation 1048882600
Related Publication 20070128097A1 · Jun 7, 2007