Production of high yields of light olefins from heavy hydrocarbons
US-11891356-B2 · Feb 6, 2024 · US
US9821299B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9821299-B2 |
| Application number | US-201213652631-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 16, 2012 |
| Priority date | Oct 17, 2011 |
| Publication date | Nov 21, 2017 |
| Grant date | Nov 21, 2017 |
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In a process for producing a phosphorus-modified zeolite catalyst, an aqueous reaction mixture comprising a source of silica and a source of an organic directing agent effective to direct the synthesis of a desired zeolite is heated at a temperature and for a time sufficient to produce crystals of the desired zeolite. Wet zeolite crystals can then be separated from the reaction mixture and, without removing all the water from the wet zeolite crystals, the zeolite can be converted into the ammonium form by ion exchange, and the crystals can be treated with a phosphorus compound. The phosphorus-treated, ammonium-exchanged zeolite can then be formed into a catalyst to be heated in one or more stages to remove the water and organic directing agent from the zeolite crystals and to convert the zeolite to the hydrogen form.
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What is claimed is: 1. A process for producing a phosphorus-modified zeolite catalyst, said process comprising: (a) heating an aqueous reaction mixture comprising a source of silica and a source of an organic directing agent effective to direct a synthesis of a ZSM-5 zeolite from said aqueous mixture, said heating being conducted at a temperature and for a time sufficient to produce crystals of the ZSM-5 zeolite; (b) separating wet zeolite crystals from the aqueous mixture produced in (a); (c) without removing all the water from the wet zeolite crystals to provide crystals having an Adsorption Factor from about 0.1 to less than 1.5, effecting the steps of: (i) converting the wet zeolite crystals into an ammonium form by ion exchange; and (ii) treating the ammonium form of the wet zeolite crystals with a phosphorus compound to produce a phosphorus-treated, ammonium-exchanged zeolite; (d) forming the phosphorus-treated, ammonium-exchanged zeolite from (c) into a catalyst; and (e) heating the catalyst in one or more stages to remove the water and organic directing agent from the zeolite crystals and to convert the zeolite crystals from the ammonium form to a hydrogen form. 2. The process of claim 1 , wherein said reaction mixture also comprises a source of alumina. 3. The process of claim 2 , wherein a molar ratio of silica to alumina in the reaction mixture is from about 20 to about 500. 4. The process of claim 2 , wherein a molar ratio of silica to alumina in the reaction mixture is from about 20 to about 150. 5. The process of claim 1 , wherein the zeolite crystals have an average crystal size of about 0.05 microns or less. 6. The process of claim 1 , wherein said organic directing agent comprises n-propylamine. 7. The process of claim 1 , wherein said temperature is from about 100° C. to about 200° C. and said time is from about 12 hours to about 120 hours. 8. The process of claim 1 , wherein the separating (b) is accomplished by filtration. 9. The process of claim 1 , wherein said wet zeolite crystals employed in (c) have an Adsorption Factor from about 0.2 to about 0.8. 10. The process of claim 1 , wherein the converting (c) (i) and the treating (c) (ii) are accomplished simultaneously. 11. The process of claim 1 , wherein the treating (c) (ii) is accomplished by impregnation. 12. The process of claim 1 , wherein the treating (c) (ii) is accomplished by impregnating the zeolite crystals with an aqueous solution of an ammonium salt of a phosphorus oxyacid. 13. The process of claim 1 , wherein the forming (d) comprises mixing the phosphorus-treated, ammonium-exchanged zeolite with a binder to form an extrudable composition and then extruding said composition to form the catalyst. 14. The process of claim 1 , wherein the heating to remove the organic directing agent from the zeolite crystals and to convert the zeolite to the hydrogen form is accomplished in a single heating step. 15. The process of claim 14 , wherein said single heating step is conducted at a temperature from about 500° C. to about 600° C. for a time from about 2 hours to about 12 hours.
Indexing scheme associated with group B01J35/00, related to the analysis techniques used to determine the catalysts form or properties · CPC title
Operations & Transport · mapped topic
Nanotechnology for materials or surface science, e.g. nanocomposites · CPC title
Operations & Transport · mapped topic
not in framework positions · CPC title
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