Sulfur resistant cladded titania—alumina supports

Patent metadata

Field	Value
Publication number	US-9409149-B2
Application number	US-201013498609-A
Country	US
Kind code	B2
Filing date	Oct 1, 2010
Priority date	Oct 8, 2009
Publication date	Aug 9, 2016
Grant date	Aug 9, 2016

Abstract

The present invention is directed to a method of forming titania clad high surface area alumina suitable as a support for forming noble metal catalysts. The resultant catalysts exhibit resistance to poisoning by sulfurous materials and, therefore, are useful in applications directed to internal combustion engine emission conversion and the like. The present invention provides a commercially feasible and cost effective method of forming a highly desired support for noble metal catalyst application. The process comprises forming a slurry of porous alumina particulate suitable as a catalyst support for the intended application, mixing said slurry with a solution of titanyl sulfate having a pH of about 1, increasing the pH of the mixed slurry/solution at a slow rate of from 0.05 to 0.5 pH unit per minute to a pH of ≦4 by the addition of a basic solution, allowing the resultant slurry to age for a period of from 10 to 120 minutes, separating the treated porous alumina particulates and washing same free of sulfate with a weak base, drying and calcining said particulates to produce titania clad alumina particulate product. The resultant material exhibits a normalized sulfur uptake of less than about 45 μg/m 2 -sample. Such material can subsequently be coated with a noble metal to form the catalyst material.

First claim

We claim:

1. A method of forming a titania clad alumina particulate comprising:
a) mixing an aqueous slurry of from about 1 to about 30 weight percent porous-alumina particulate with an aqueous solution of titanyl sulfate having a pH of from about 0.5 to 1.5 for a period of time to provide a uniform mixture;
b) raising the pH of the mixture at a rate of from 0.05 to 0.5 pH unit/minute to a resultant pH of between 3.4 and 4 by the addition of an aqueous basic solution;
c) allowing the resultant slurry to remain at said resultant pH for a period of from about 10 to 120 minutes;
d) removing sulfate ions from the treated solid particulate to form a material comprising less than 0.5% sulfate;
e) drying the solid particulate followed by heating said solid particulate at from about 400° to 1000° C. for a period of from about 15 to 480 minutes; and
f) recovering solid titania clad alumina particulate.

2. The method of claim 1 wherein the initially formed uniform mixture of porous alumina particulate and titanyl sulfate has a concentration of titanyl sulfate in a ratio of titanyl sulfate (calculated as titania) to total oxides of from 1 to 50 and has a pH of from 0.5 to 1.5.

3. The method of claim 1 wherein the pH of the uniform mixture is raised from the initial pH 0.9 to 1.2 to a pH range of from 3.5 to 4 at a rate of 0.05 to 0.25 pH unit per minute under constant agitation followed by maintaining said mixture at said raised-pH for from about 15 to 60 minutes.

4. The method of claim 1 wherein the base of the aqueous basic solution of b) is selected from ammonium hydroxide, ammonium carbonate, ammonium bicarbonate, an alkali metal hydroxide, an alkali metal carbonate, an alkali metal bicarbonate an alkaline earth metal hydroxide, an alkaline earth metal carbonate, an alkaline earth metal bicarbonate, a tri(C 1 -C 3 )alkyl ammonium compound, a mono-, di- or tri-(C 1 -C 3 ) alkanolamines or mixtures thereof.

5. The method of claim 4 wherein the base is selected from ammonium hydroxide, ammonium carbonate, ammonium bicarbonate or mixtures thereof.

6. The method of claim 1 wherein the sulfate ions are removed from the treated solid particulate of d) by contacting said solid particulate with sufficient amount of water, ammonium hydroxide, ammonium carbonate, ammonium bicarbonate, an alkali metal hydroxide or mixtures thereof.

7. The method of claim 6 wherein the solid particulate is treated with an aqueous solution of ammonium carbonate, ammonium bicarbonate or mixtures thereof.

8. The method of claim 6 or 7 wherein the solid particulate of e) is dried to a powder material and then heated to a temperature of from about 600 to 800° C. for a period of from 1 to 4 hours.

9. A titania clad alumina particulate formed by the process of claim 1 , 2 , 3 , 4 , 5 , 6 , or 7 and having an NSU of less than 45 μg/m 2 -sample.

10. A titania clad alumina particulate formed by the process of claim 8 having an NSU of less than 45 μg/m 2 -sample.

11. The product of claim 9 wherein the titania clad alumina particulate has an average particle size of from 1 to 200 μm.

12. The product of claim 10 wherein the titania clad alumina particulate has an average particle size of from 1 to 200 μm.

Assignees

• Koranne Manoj Mukund
• Chapamn David
• Grace W R & Co

Inventors

• Koranne Manoj Mukund
• Chapamn David

Classifications

• C01F7/02

  Aluminium oxide; Aluminium hydroxide; Aluminates · CPC title

• B01J23/40

  of the platinum group metals · CPC title

• B01J23/10

  of rare earths · CPC title

• B01D2255/20707

  Titanium · CPC title

• B01D2255/90

  Physical characteristics of catalysts · CPC title