ITQ-49 material, method for the production thereof and use of same
US-9764311-B2 · Sep 19, 2017 · US
US10427140B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10427140-B2 |
| Application number | US-201715678636-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 16, 2017 |
| Priority date | Apr 18, 2012 |
| Publication date | Oct 1, 2019 |
| Grant date | Oct 1, 2019 |
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The present invention refers to a microporous crystalline material, to the method for the production thereof and to the use of same, the material having a composition: x X 2 O 3 :z ZO 2 :y YO 2 in which: X is a trivalent element such as Al, B, Fe, In, Ga, Cr, or mixtures thereof, where (y+z)/x can have values of between 9 and infinity; Z corresponds to a tetravalent element selected from Si, Ge or mixtures thereof; and Y corresponds to a tetravalent element such as Ti, Sn, Zr, V or mixtures thereof, where z/y can have values of between 10 and infinity.
Opening claim text (preview).
The invention claimed is: 1. A process for the preparation of a material, comprising at least the following steps: a) preparing a mixture containing H 2 O, a source of fluoride ions, an oxide or another source of the tetravalent material Z and a structure directing agent (R), a source of the trivalent element X, an oxide or other source of the tetravalent material Y, wherein the synthesis mixture has a molar composition of oxides within the following ranges: (YO 2 + ZO 2 )/X 2 O 3 higher than 2 H 2 O/(YO 2 + ZO 2 ) 1-50 R/(YO 2 + ZO 2 ) 0.05-3.0 F − /(YO 2 + ZO 2 ) 0.01-3.0 ZO 2 /YO 2 higher than 5 SiO 2 /GeO 2 higher than 1 b) maintaining the mixture at a temperature between 80 and 200° C. until crystals of the material are formed; c) recovering the crystalline material; wherein the microporous crystalline material has the following chemical composition: x X 2 O3 : yYO 2 : zZO 2 , wherein: X is a trivalent element selected from Al, B, Fe, In, Ga, Cr, or mixtures thereof; Y is a tetravalent element tetravalent selected from Ti, Sn, Zr, V or mixtures thereof; Z is a tetravalent element tetravalent selected from Si, Ge and mixtures thereof the value of (y+z)/x is comprised between 9 and infinity; the value of z/y is comprised between 10 and infinity; and an X-ray diagram shown in Table 3. 2. The process for the preparation of a material according to claim 1 , wherein Z is Si, Ge or a mixture of both. 3. The process for the preparation of a material according to claim 1 , wherein the strucure directing agent R is a compound that contains P. 4. The process for the preparation of a material according to claim 3 , wherein R is an alkylphosphonium salt. 5. The process for the preparation of a material according to claim 4 , wherein R is 1,4-butanediyl-bis(tritertbutyl)phosphonium hydroxide or one of its salts. 6. The process for the preparation of a material according to claim 1 , that further comprises the calcination of the crystalline material obtained. 7. The process for the preparation of a material according to claim 6 , wherein the calcination is carried out at a temperature between 200 and 1200° C. 8. The process for the preparation of a material according to claim 1 , that further comprises one or more post-synthesis processes. 9. The process for the preparation of a material according to claim 8 , wherein said post-synthesis treatment comprises at least: a) suspending the material in a solution that contains at least a trivalent element X selected from the group consisting of Al, Ga, B, Cr, Fe, In and mixtures thereof; b) recovering of the solid through filtration, centrifugation or any other technique for solids-liquids separation; c) activating the material through calcination at temperatures higher than 200° C. 10. The process for the preparation of a material according to claim 9 , wherein the solution is selected from the group consisting of an aqueous solution, an alcoholic solution, an organic solution and mixtures thereof. 11. The process for the preparation of a material according to claim 9 , wherein the post-synthesis treatment is carried out at a temperature between 0 and 200° C. 12. Method of catalysing a reaction comprising subjecting the reagents to a catalyst comprising a microporous crystalline material, having a chemical composition: x X 2 O 3 :y YO 2 :z ZO 2 wherein: X is a trivalent element selected from Al, B, Fe, In, Ga, Cr, or mixtures thereof; Y is a tetravalent element tetravalent selected from Ti, Sn, Zr, V or mixtures thereof; Z is a tetravalent element tetravalent selected from Si, Ge and mixtures thereof; the value of (y+z)/x is comprised between 9 and infinity; the value of z/y is comprised between 10 and infinity; and an X-ray diagram shown in Table 3. 13. Method of catalysing according to claim 12 , wherein said material was obtained through a process comprising at least the following steps: a) preparing a mixture containing H 2 O, a source of fluoride ions, an oxide or another source of the tetravalent material Z and a structure directing agent (R), a source of the trivalent element X, an oxide or other source of the tetravalent material Y, wherein the synthesis mixture has a molar composition of oxides within the following ranges: (YO 2 + ZO 2 )/X 2 O 3 higher than 2 H 2 O/(YO 2 + ZO 2 ) 1-50 R/(YO 2 + ZO 2 ) 0.05-3.0 F − /(YO 2 + ZO 2 ) 0.01-3.0 ZO 2 /YO 2 higher than 5 SiO 2 /GeO 2 higher than 1 b) maintaining the mixture at a temperature between 80 and 200° C. until crystals of the material are formed; c) recovering the crystalline material. 14. Method of converting hydrocarbons comprising subjecting the hydrocarbons to a catalyst comprising the material described in claim 12 . 15. Method of dewaxing hydrocarbons comprising subjecting the hydrocarbons to a catalyst comprising the material described in claim 12 . 16. Method of converting hydrocarbons comprising subjecting the alcohols to a catalyst comprising the material described in claim 12 . 17. Method for converting alcohols with less than four carbon atoms, into olefins comprising subjecting said alcohols to a catalyst comprising the material described in claim 12 . 18. Method for removing nitrogenated pollutants in gaseous or liquid streams comprising subjecting said gaseous or liquid streams to a catalyst comprising the material described in claim 12 . 19. Method for removing nitrogen oxides in gaseous streams comprising subjecting said gaseous stream to a catalyst comprising the material described in claim 12 . 20. Method for removing nitrogen oxides in gaseous streams
comprising silica or silicate · CPC title
Phosphates, e.g. APO or SAPO compounds · CPC title
of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65 · CPC title
by reduction · CPC title
Zeolites · CPC title
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