Direct synthesis of a microporous aluminosilicate material having an AFX structure and comprising copper, and use of said material

1. A process for preparing a copper-containing microporous aluminosilicate material with AFX structure, comprising at least the following steps:

a) mixing, in an aqueous medium, of at least one aluminum source, at least one silicon source, sodium hydroxide, at least one copper source, an organic complexing agent (OCPLX) chosen from triethylenetetramine (TETA) or tetraethylenepentamine (TEPA) and a structuring agent 1,4-diazabicyclo[2.2.2]octane-C4-diquat dibromide (DABCO-C4), in order to obtain a gel of molar composition:

a SiO 2 :b Al 2 O 3 :c Na 2 O: d DABCO-C4 :e CuO: f OCPLX: g H 2 O

a/b being between 100 and 40, c/b being between 25 and 50, d/b being between 3 and 10, e/b being between 0.05 and 0.1, f/e being between 1 and 1.5 and g/b being between 4000 and 1000;

b) hydrothermal treatment of the gel at a temperature of between 130 and 180° C., under an autogenous reaction pressure, for a period of between 1 and 8 days with stirring in order to obtain the crystallization of the copper-comprising microporous aluminosilicate material with AFX structure;

c) drying heat treatment of the solid obtained at the end of the preceding step at a temperature of between 80 and 120° C. under a stream of inert gas followed by calcining under dry air at a temperature of between 400 and 600° C.;

d) ion exchange comprising bringing the solid obtained the end of the preceding step into contact with a solution comprising a species capable of releasing copper in solution in reactive form with stirring at ambient temperature for a period of between 1 h and 2 d;

e) drying heat treatment of the solid obtained at the end of the preceding step at a temperature of between 80 and 120° C. followed by calcining under a stream of inert gas and then air at a temperature of between 400 and 600° C.;

the total amount of copper contained in the material obtained at the end of the preparation process being between 1.5 and 5.75% by weight relative to the total weight of the material in its anhydrous form.

2. The process as claimed in claim 1 , wherein steps c) and d) are inverted.

3. The process as claimed in claim 1 , wherein the amount of copper introduced during step a) represents between 0.75 and 2%, the amount of copper introduced during step d) representing between 0.75 and 5%, the amount of copper contained in the material being ultimately between 1.5 and 5.75%, all the percentages being percentages by weight relative to the total weight of the material in its anhydrous form obtained at the end of the preparation process.

4. The process as claimed in claim 1 , wherein a maturation step at ambient temperature is carried out at the end of step a) and before step b).

5. The process as claimed in claim 4 , wherein the step b) is carried out at a temperature of between 140 and 170° C.

6. The process as claimed in claim 1 , wherein the step b) is carried out for a period of between 3 and 6 days.

7. The process as claimed in claim 1 , wherein the step b) is carried out with stirring with a rotation of the stirring shaft of between 100 and 4000 rotations per minute.

8. The process as claimed in claim 1 , wherein the step b) is carried out with stirring with a rotation of the stirring shaft of between 200 and 2000 rotations per minute.

9. The process as claimed in claim 1 , wherein the dry air flow rate of the calcination treatment in the course of the step c) is between 0.5 and 1.5 Whig of solid to be treated.

10. A copper-comprising microporous aluminosilicate material with AFX structure obtained by a process as claimed in claim 1 .

11. A method comprising selectively reducing NO x with a reducing agent in the presence of the copper-comprising microporous aluminosilicate with AFX structure as claimed in claim 10 .

12. The method as claimed in claim 11 , wherein the copper-comprising microporous aluminosilicate material with AFX structure is formed by deposition in the form of a coating on a honeycomb structure.

13. The method as claimed in claim 12 , wherein the coating comprises the material in combination with a binder comprising cerine, zirconium oxide, alumina, non-zeolite silica-alumina, titanium oxide, a cerine-zirconia mixed oxide, or a tungsten oxide.

14. The method as claimed in claim 12 , wherein the coating is in combination with another coating having NO x reducing capacities or capacities which promote the oxidation of pollutants.

15. The method as claimed in claim 11 , wherein a structure coated by the material is integrated in an exhaust line of an internal combustion engine.

16. The method as claimed in claim 11 , wherein the reducing agent is NH 3 or H 2 .