METHOD FOR THE PREPARATION OF A ZONE COATED CATALYSED MONOLITH

Abstract

Method for zone coating of monolithic substrates by using different sol-solution containing different catalyst carrier precursors and metal catalyst precursors and suction of one of the sol-solution up into pores in the walls of the zone to be coated, solely by capillary forces and another different sol-solution into the walls of another zone to be coated by capillary forces.

Claims

1. A method for the preparation of a catalysed monolith zone coated with different catalysts, comprising the steps of a) providing a porous monolith substrate with a plurality of longitudinal flow channels separated by gas permeable partition walls, the monolith substrate having a first end face and at a distance to the first end face a second end face; b) providing a first sol solution in an amount corresponding to at least the pore volume in a first catalyst zone of the gas permeable partition walls to be coated with the first sol solution, the first sol solution containing water soluble or suspended precursors of one or more catalytically active compounds and water soluble or suspended precursors or oxides of one or metal oxides catalyst carrier compounds, at least one of the one or more precursors or oxides is suspended and at least one of the one or more precursors is dissolved in the sol solution; c) providing a second sol solution in an amount corresponding to at least the pore volume in a second catalyst zone of the gas permeable partition walls to be coated with the second sol solution, the second sol solution containing water soluble or suspended precursors of one or more catalytically active compounds different to the catalytically active compounds in the first sol solution and water soluble or suspended precursors or oxides of one or more metal oxides catalyst carrier compounds, at least one of the one or more precursors or oxides is suspended and at least one of the one or more precursors is dissolved in the second sol solution; d) placing the porous monolith substrate substantially vertically in a container containing the amount of the first sol solution and dipping the first end face facing the first catalyst zone into the first sol solution; e) sucking up the amount of the first sol solution solely by capillary forces into pores of the permeable partition walls from the first end face without applying vacuum or pressure into pores of the first zone; f) subsequently inverting the porous monolith substrate and placing the porous monolith substrate substantially vertically in a container containing the amount of the second sol solution dipping the second end face facing the second catalyst zone into the second sol solution; g) sucking up the amount of the second sol solution solely by capillary forces into pores of the permeable partition walls from without applying vacuum or pressure into pores of the second zone; and h) drying and calcining the thus coated monolith substrate.

2. The method of claim 1, wherein the porous monolith substrate is a wall flow filter.

3. The method of claim 1, wherein the one or more catalytically active precursors in the first or second sol solution are selected from the group consisting of compounds of palladium, platinum, rhodium, vanadium, molybdenum, tungsten and mixtures thereof

4. The method of claim 1, wherein the precursors of the one or more metal oxides catalyst carrier in the first or second sol solution are selected from the group consisting of compounds of aluminium, titanium, cerium, zirconium, silicon and mixtures thereof

5. The method of claim 1, wherein the porous monolith substrate is metallic or ceramic.

6. The method of claim 1, wherein the porous monolith substrate consists of cordierite or silicon carbide or aluminium titanate or mullite.

7. The method of claim 1, wherein particle size of the suspended precursors of one or more catalytically active compounds and the suspended precursors or oxides of one or more metal oxides catalyst carrier compounds is between 1 and 500 nm.

8. The method of claim 1, wherein particle size of suspended precursors of one or more catalytically active compounds and the suspended precursors or oxides of one or more metal oxides catalyst carrier compounds is between 1 and 100 nm.

9. The method of claim 1, wherein the sucking up steps e and/or g are repeated once or more times.

10. The method of claim 1, any one of the preceding claims comprising a further step of drying the monolith substrate between step e and f.

11. The method of claim 10, wherein the dried monolith substrate is calcined prior to step g.

Description

[0015] Thus, the invention provides a method for the preparation of a catalysed monolith zone coated with different catalysts, comprising the steps of

[0016] a) providing a porous monolith substrate with a plurality of longitudinal flow channels separated by gas permeable partition walls, the monolith substrate having a first end face and at a distance to the first end face a second end face;

[0017] b) providing a first sol solution in an amount corresponding to at least the pore volume in a first catalyst zone of the gas permeable partition walls to be coated with the first sol solution, the first sol solution containing water soluble or suspended precursors of one or more catalytically active compounds and water soluble or suspended precursors or oxides of one or metal oxides catalyst carrier compounds, at least one of the one or more precursors or oxides is suspended and at least one of the one or more precursors is dissolved in the sol solution;

[0018] c) providing a second sol solution in an amount corresponding to at least the pore volume in a second catalyst zone of the gas permeable partition walls to be coated with the second sol solution, the second sol solution containing water soluble or suspended precursors of one or more catalytically active compounds different to the catalytically active compounds in the first sol solution and water soluble or suspended precursors or oxides of one or more metal oxides catalyst carrier compounds, at least one of the one or more precursors or oxides is suspended and at least one of the one or more precursors is dissolved in the second sol solution;

[0019] d) placing the porous monolith substrate substantially vertically in a container containing the amount of the first sol solution and dipping the first end face facing the first catalyst zone into the first sol solution;

[0020] e) sucking up the amount of the first sol solution solely by capillary forces into pores of the permeable partition walls from the first end face without applying vacuum or pressure into pores of the first zone;

[0021] f) subsequently inverting the porous monolith substrate and placing the porous monolith substrate substantially vertically in a container containing the amount of the second sol solution dipping the second end face facing the second catalyst zone into the second sol solution;

[0022] g) sucking up the amount of the second sol solution solely by capillary forces into pores of the permeable partition walls from without applying vacuum or pressure into pores of the second zone; and

[0023] h) drying and calcining the thus coated monolith substrate.

[0024] The sol solution for use in the invention is typically formulated from metal oxide precursors of ceria, alumina, titania, zirconia, silica sols in combination with dissolved catalytically active metal precursor, preferably compounds of palladium, platinum, rhodium, vanadium, molybdenum, tungsten and mixtures thereof in a liquid dispersion agent, typically aqueous solutions of acids.

[0025] Preparation of the sol solution involves conversion of monomers into a colloidal solution that acts as the precursor of discrete particles of the metal oxides catalyst carrier and catalytically active metal compounds. Typical precursors are metal nitrates and stabilized metal hydroxides or oxyhydroxides. Ammonium compounds are typical stabilizers. The acidity of the sol solution is adjusted to a pH value, where the sol is stable and does not form a gel.

[0026] The particle size of the suspended precursors is between 1-500 nm, preferably between 1-100 nm. The size of the suspended particles is significant less than the pore size diameter in the monolith walls, namely typically 1-30 ?m.

[0027] In order to provide the correct amount of the sol-solution, the pore volume of the zone to be coated in the monolithic substrate is determined prior to coating of the monolithic substrate. Determination of the pore volume is carried out by conventional methods known in the art.

[0028] By the method according to the invention, the sol solution is sucked up and adsorbed within the pores of monolith substrate by solely capillary forces without in the zone(s) of the monolith substrate on the walls of the substrate upwardly from the end face dipped into the sol solution without the assistance of external forces like vacuum or pressure applied on the end faces. The wetted length of the substrate that is the distance between the wetted end of the substrate and the wet front is dependent on the porosity of the substrate. The wetted length is also dependent on the liquid-air surface tension. The liquid-air tension decreases at increasing temperatures. It is therefore preferred to perform the wetting process at low temperatures, most preferably between 15 and 30? C.

[0029] As already mentioned above, the method according to the invention is in particular useful for coating different zones of a wall flow filter with the sol solution containing different kind of catalysts or the same kind of catalysts in different concentrations.

[0030] The sucking up steps can be repeated once or more times.

[0031] It might be preferred to dry and calcine the monolith substrate between the different sucking up steps.

[0032] Application of microwaves can advantageously be used in the drying step.

[0033] The monolithic substrate can in all cases be made of porous ceramic material or porous metallic material.

[0034] Preferably, the monolith substrate consists of cordierite or silicon carbide or aluminium titanate or mullite.