Cerium- and zirconium-based mixed oxide

Patent metadata

Field	Value
Publication number	US-11547982-B2
Application number	US-201716096280-A
Country	US
Kind code	B2
Filing date	Apr 25, 2017
Priority date	Apr 26, 2016
Publication date	Jan 10, 2023
Grant date	Jan 10, 2023

Abstract

The invention relates to a mixed oxide composed of zirconium, cerium, lanthanum and at least one rare earth oxide other than cerium and lanthanum, having a specific porosity and a high specific surface area; to the method for preparing same and to the use thereof in catalysis.

First claim

The invention claimed is:

1. A mixed oxide of zirconium, of cerium, of lanthanum and optionally of at least one rare earth metal other than cerium and lanthanum (REM), the proportions by weight of these elements, expressed as oxide equivalent, with respect to the total weight of the mixed oxide being as follows:
between 8% and 45% of cerium;
between 1% and 10% of lanthanum;
between 0% and 15% of the rare earth metal other than cerium and lanthanum;
the remainder as zirconium,
characterized in that the mixed oxide exhibits:
after calcination at a temperature of 1100° C. for 4 hours, a BET specific surface of at least 30 m 2 /g;
after calcination at a temperature of 1000° C. for 4 hours, a BET specific surface of at least 55 m 2 /g;

characterized in that the derivative curve (dV/dlogD) obtained by mercury porosimetry on the mixed oxide after calcination at a temperature of 1100° C. for 4 hours exhibits, in the range of the pores with a diameter of less than or equal to 200 nm, a peak for which the maximum corresponds to a pore diameter, denoted D p,1100° C./4 h , of between 24 and 34 nm, V and D respectively denoting the pore volume and the pore diameter;
and characterized in that the ratio R is defined by:

R
=

V
1

V
2

in which:
V 1 is the pore volume developed by the pores for which the diameter in nm is between (D p,1100° C./4 h −15) and (D p,1100° C./4 h +15);
V 2 is the pore volume developed by the pores for which the diameter is less than or equal to 200 nm;
V 1 and V 2 being determined by mercury porosimetry on the mixed oxide after calcination at 1100° C. for 4 h; and
is greater than or equal to 0.60.

2. The mixed oxide as claimed in claim 1 , characterized in that it also comprises hafnium.

3. The mixed oxide as claimed in claim 2 , characterized in that the proportion by weight of hafnium in the mixed oxide is less than or equal to 2.5%, expressed as oxide equivalent with respect to the total weight of the mixed oxide.

4. The mixed oxide as claimed in claim 2 , characterized in that the elements Ce, La, REM, Zr and Hf are present in the form of oxides, of hydroxides or of oxyhydroxides.

5. The mixed oxide as claimed in claim 1 , consisting of the following elements:
zirconium and optionally hafnium, cerium, lanthanum, yttrium; or
zirconium and optionally hafnium, cerium, lanthanum, yttrium, neodymium; or
zirconium and optionally hafnium, cerium, lanthanum, yttrium, praseodymium; or
zirconium and optionally hafnium, cerium, lanthanum.

6. The mixed oxide as claimed in claim 1 , further comprising tin in the oxide form SnO 2 in a proportion by weight, as oxide equivalent, with respect to the total weight of the mixed oxide, of strictly less than 1.0%.

7. The mixed oxide as claimed in claim 1 , characterized in that the proportion by weight of the zirconium as oxide equivalent is, putting aside oxygen, greater than the proportion by weight as oxide equivalent of each of the other constituent elements of the mixed oxide.

8. The mixed oxide as claimed in claim 1 , characterized in that the proportion by weight of the zirconium, expressed as oxide equivalent, is between 40% and 91%.

9. The mixed oxide as claimed in claim 1 , characterized in that the rare earth metal other than cerium and lanthanum is chosen from yttrium, neodymium or praseodymium.

10. The mixed oxide as claimed in claim 1 , not comprising a rare earth metal other than cerium and lanthanum.

11. The mixed oxide as claimed in claim 1 , comprising only yttrium as rare earth metal other than cerium and lanthanum.

12. The mixed oxide as claimed in claim 1 , comprising only two rare earth metals other than cerium and lanthanum.

13. The mixed oxide as claimed in claim 1 , characterized in that the pore diameter D p,1100° C./4 h of the mixed oxide is between 24 nm and 30 nm, this upper value being excluded.

14. The mixed oxide as claimed in claim 1 , characterized in that the derivative curve (dV/dlogD) obtained by mercury porosimetry on the mixed oxide after calcination at a temperature of 900° C. for 4 hours exhibits, in the range of the pores with a diameter of less than or equal to 200 nm, a peak for which the maximum corresponds to a pore diameter D p,900° C./4 h and such that the difference in absolute value D p,1100° C./4 h −D p,900° C./4 h is less than or equal to 15 nm.

15. The mixed oxide as claimed in claim 1 , exhibiting, after calcination at a temperature of 900° C. for 4 hours, a BET specific surface of at least 60 m 2 /g.

16. The mixed oxide as claimed in claim 1 , which is provided in the form of a powder having a mean diameter d 50 of between 0.5 and 50.0 μm, as determined by laser diffraction over a distribution by volume.

17. The mixed oxide as claimed in claim 1 , characterized in that the derivative curve (dV/dlogD), obtained by mercury porosimetry on the mixed oxide after calcination at a temperature of 900° C. for 4 hours, does not exhibit two peaks within the range of the pores for which the diameter is less than or equal to 200 nm.

18. The mixed oxide as claimed in claim 1 , characterized in that the ratio R is greater than or equal to 0.7.

19. A process for the preparation of the mixed oxide as claimed in claim 1 , comprising the following steps:
(a1) introducing an aqueous solution of cerium nitrate and of zirconium nitrate into a stirred vessel containing a basic aqueous solution to form a mixture;
(a2) subsequently introducing an aqueous solution of lanthanum nitrate and of nitrate of the rare earth metal (REM) optionally present in the mixed oxide into the mixture formed in step (a1), while stirring, to form a suspension;
(a3) heating the suspension obtained at the end of step (a2) while stirring;
(a4) subsequently introducing a templating agent into the suspension obtained in the preceding step;
(a5) filtering the suspension to obtain a precipitate and washing the precipitate;
(a6) calcining the precipitate obtained at the end of step (a5) at a temperature of between 700° C. and 1100° C. to give the mixed oxide;
(a7) optionally grinding the mixed oxide obtained in step (a6).

20. A composition comprising the mixed oxide as claimed in claim 1 and at least one mineral material.

21. The composition as claimed in claim 20 , in which the mineral material is chosen from alumina, titanium oxide, cerium oxide, zirconium oxide, silica, spinels, zeolites, silicates, crystalline silicoaluminum phosphates or crystalline aluminum phosphates.

22. A catalytically active coating layer, deposited at the surface of a solid support, prepared from the mixed oxide as described in claim 1 .

23. A catalytic converter for treating motor vehicle exhaust gases, comprising a coating layer as claimed in claim 22 .

24. A process for the treatment of exhaust gases from internal combustion engines, the process comprising contacting the exhaust gases with a catalytic converter comprising a coating layer as claimed in claim 22 .

25. A mixed oxide consisting of a mixture of oxides of zirconium, of cerium, of lanthanum, optionally of at least one rare earth

Assignees

• Rhodia Operations

Inventors

• Jorge Coelho Marques Rui Miguel
• Ifrah Simon
• Chabert Boris

Classifications

• C01P2004/61

  Micrometer sized, i.e. from 1-100 micrometer · CPC title

• C01P2004/51

  Particles with a specific particle size distribution · CPC title

• B01D2255/2094

  Tin · CPC title

• C01G25/02 Primary

  Oxides · CPC title

• C01P2006/17

  Pore diameter distribution · CPC title