Catalyst manufacturing method

Patent metadata

Field	Value
Publication number	US-10843174-B2
Application number	US-201515536382-A
Country	US
Kind code	B2
Filing date	Dec 18, 2015
Priority date	Dec 19, 2014
Publication date	Nov 24, 2020
Grant date	Nov 24, 2020

Abstract

A method for producing a catalyst or catalyst precursor is described including: applying a slurry of a particulate catalyst compound in a carrier fluid to an additive layer manufactured support structure to form a slurry-impregnated support, and drying and optionally calcining the slurry-impregnated support to form a catalyst or catalyst precursor. The mean particle size (D50) of the particulate catalyst compound in the slurry is in the range 1-50 μm and the support structure has a porosity ≥0.02 ml/g.

First claim

The invention claimed is:

1. A method for producing a catalyst or catalyst precursor comprising:
(i) combining particles of a support material with a binder to form a particulate preform mixture, wherein (a) the binder is a particulate binder material in which case the particulate preform mixture comprises a blended particulate mixture of the support material particles and the particulate binder material or (b) the binder is applied as a coating to the surface of the particles of the support material, in which case the particulate preform mixture comprises the support material particles coated with the binder coating;
(ii) forming a layer of the particulate preform mixture;
(iii) applying a binding solvent from a print-head to the layer of particulate preform mixture according to a predetermined pattern, wherein the binding solvent dissolves the binder contacted by the binder solvent, thereby causing the binder contacted by the binding solvent to dissolve and then bind the particulate support material together according to the pre-determined pattern, and leaving the particles of the support material and binder not contacted by the binding solvent as unbound particulate material;
(iv) repeating (ii) and (iii) layer upon layer;
(v) removing the unbound particulate material;
(vi) drying and optionally calcining to form a support structure;
(vii) applying a slurry of a particulate catalyst compound in a carrier fluid to the support structure to form a slurry-impregnated support; and
(viii) drying and optionally calcining the slurry-impregnated support to form a catalyst or catalyst precursor, wherein the mean particle size (D50) of the particulate catalyst compound in the slurry is in the range of from 1 to 50 μm and the support structure has a porosity of 0.02 ml/g or greater.

2. The method of claim 1 , wherein the particles of the support material have a particle size in a range of from 0.1 micron to 400 microns.

3. The method of claim 1 , wherein the particles of the support material comprise an alumina, metal-aluminate, silica, alumino-silicate, cordierite, titanium (IV) oxide, zirconia, cerium (IV) oxide, zinc oxide, or a mixture thereof, a zeolite, a metal powder, silicon carbide, silicon nitride, or carbon.

4. The method of claim 1 , wherein the particles of the support material comprises one or more of a hydrous alumina, transition alumina, alpha alumina, or metal-aluminate.

5. The method of claim 1 , wherein the binder is dextrin, sucrose, or a mixture thereof or PVA.

6. The method of claim 1 , wherein the particulate preform mixture contains polymer or ceramic fibres in a range of from 1% to 10% by weight, relative to the weight of the particulate preform mixture.

7. The method of claim 1 , wherein the particulate preform mixture contains one or more sintering aids that are titanium oxide, iron oxide, copper oxide, magnesium oxide, or calcium carbonate in a range of from 0.5% to 5% by weight, relative to the weight of the particulate preform mixture.

8. The method of claim 7 , wherein the sintering aid is a mixture of titanium (IV) oxide and iron (III) oxide, or a mixture of titanium (IV) oxide and copper (II) oxide.

9. The method of claim 8 , wherein the weight ratio range of TiO 2 to Fe 2 O 3 or TiO 2 to CuO is in a range of from 40:60 to 60:40.

10. The method of claim 1 , wherein the layers of preform material each have a thickness in the range of from 0.02 to 5.0 mm.

11. The method of claim 10 , wherein each of the layers of preform material have a thickness in the range of from 0.02 mm to 2.5 mm.

12. The method of claim 1 , wherein the binding solvent is an organic solvent or water.

13. The method of claim 1 , wherein the printing head is used at printing resolution in the x-direction in the range of from 40 μm to 70 μm and in the y-direction of 80 to 100 μm for layer thicknesses in the range of from 50 to 150 μm.

14. The method of claim 1 , wherein the dried support structure is subjected to a calcination stage at a temperature in the range of from 500° C. to 2000° C.

15. The method of claim 1 , wherein the slurry has a solids content in the range of from 5 to 80% by weight, relative to the weight of the slurry.

16. The method of claim 1 , wherein the particulate catalyst compound applied to the support structure comprises a metal powder, metal compound, or a zeolite.

17. The method of claim 16 , wherein the particulate catalyst compound applied to the support structure comprises a metal oxide, metal hydroxide, metal carbonate, metal hydroxycarbonate or mixture thereof of one or more of Na, K, Mg, Ca, Ba, Al, Si, Sn, Sb, Pb, or Ce.

18. The method of claim 1 , wherein the particulate catalyst compound comprises a precious metal powder that is one or more of Pt, Pd, Rh, Ir, Ru, or Re.

19. The method of claim 1 , wherein the particulate catalyst compound is one or more transition metal compound.

20. The method of claim 19 , wherein the transition metal compound comprises one or more of Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Ru, Rh, Pd, Ag, La, Hf, W, Re, Ir, Pt, Au, or Ce.

21. The method of claim 19 , wherein the transition metal compound is a transition metal oxide, transition metal hydroxide, transition metal carbonate, transition metal hydroxycarbonate or mixture thereof.

22. The method of claim 19 , wherein the particulate catalyst compound is a bulk catalyst particle in which the catalytic metal is distributed throughout the particle or is a coated catalyst particle in which the catalytic metal is present as a surface layer on the surfaces of the particle.

23. The method of claim 19 , wherein the particulate catalyst compound comprises one or more of Pt, Pd, Rh, or Ir coated onto a support material.

24. The method of claim 19 , wherein the particulate catalyst compound is a coated or bulk catalyst comprising one or more of Ni, Co, Mo, W, Cu, or Fe.

25. The method of claim 19 , wherein the particulate catalyst compound is LaCoO 3 , LaCoO 3 in which partial substitution of the A-site has been made by Sr or Ce, zirconia or a mixture thereof, or Co 3 O 4 promoted by rare earth elements.

26. The method of claim 1 , wherein the support has a porosity of in a range of from 0.02 ml/g to 1.4 mL/g.

27. The method of claim 1 , wherein the particles of the support material are porous, having a pore size distribution (D50) in a range of from 10 microns to 25 microns.

28. The method of claim 1 , wherein the mean particle size (D50) of the particulate catalyst compound in the slurry is in the range of from 1 micron to 50 microns.

29. The method of claim 1 , wherein the particles of the support material are porous, having a pore size distribution (D50), and the mean particle size (D50) of the particulate catalyst compound is less than the pore size distribution (D50) of the particles of support material.

Assignees

• Johnson Matthey Plc
• Johnson Mattey Plc

Inventors

• Coupland Duncan Roy
• Phillips Jonathan David
• Winfield Sophie

Classifications

• B22F2007/066

  using impregnation · CPC title

• B22F2007/047

  non-pressurised baking of the paste or slurry containing metal powder · CPC title

• B22F7/08

  with one or more parts not made from powder {(B22F7/062 takes precedence)} · CPC title

• B22F7/002

  of porous nature · CPC title

• B22F3/26

  Impregnating {(making ferrous alloys by impregnation C22C33/0242)} · CPC title