Hydrocracking catalyst for hydrocarbon oil, method for producing hydrocracking catalyst, and method for hydrocracking hydrocarbon oil with hydrocracking catalyst
US-9221036-B2 · Dec 29, 2015 · US
US9944863B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9944863-B2 |
| Application number | US-201615291823-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 12, 2016 |
| Priority date | Apr 24, 2014 |
| Publication date | Apr 17, 2018 |
| Grant date | Apr 17, 2018 |
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The present invention is directed to an improved hydrocracking catalyst containing an amorphous silica-alumina (ASA) base and alumina support. The ASA base is characterized as having a high nanopore volume and low particle density. The alumina support is characterized as having a high nanopore volume. Hydrocracking catalysts employing the combination high nanopore volume ASA base and alumina support exhibit improved hydrogen efficiency, and greater product yield and quality, as compared to hydrocracking catalysts containing conventional ASA base and alumina components.
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What is claimed is: 1. A hydrocracking catalyst, comprising: a base extrudate comprising at least one molecular sieve, an alumina and an amorphous silica alumina support, wherein the base extrudate has one or more of the following: a nanopore volume in the 6 nm to 11 nm range of 0.5 to 0.9 cc/g, a total nanopore volume in the 2 to 50 nm of 0.7 to 1.2 cc/g, a particle density of 0.7 to 0.9 g/cc; or the base extrudate is formed using an amorphous silica alumina support having a nanopore volume in the 6 nm to 11 nm range of 0.6 to 0.9 cc/g; and at least one metal selected from the group consisting of elements from Group 6 and Groups 8 through 10 of the Periodic Table. 2. The hydrocracking catalyst of claim 1 , wherein the base extrudate is formed using an alumina having a nanopore volume in the 6 nm to 11 nm range of 0.1 to 0.3 cc/g. 3. The hydrocracking catalyst of claim 2 , wherein the base extrudate is formed using an amorphous silica alumina support having a nanopore volume in the 6 nm to 11 nm range of 0.6 to 0.9 cc/g. 4. The hydrocracking catalyst of claim 1 , wherein the base extrudate is formed using an amorphous silica alumina support having a nanopore volume in the 6 nm to 11 nm range of 0.6 to 0.9 cc/g. 5. The hydrocracking catalyst of claim 1 , wherein the base extrudate has a total nanopore volume in the 2 to 50 nm of 0.7 to 1.2 cc/g. 6. The hydrocracking catalyst of claim 1 , wherein the base extrudate has a particle density of 0.7 to 0.9 g/cc. 7. The hydrocracking catalyst of claim 1 , wherein the base extrudate has a nanopore volume in the 6 nm to 11 nm range of 0.6 to 0.9 cc/g. 8. A method for making a hydrocracking catalyst, comprising the steps of: forming a base extrudate comprising at least one molecular sieve, an alumina and an amorphous silica alumina support, wherein the base extrudate has one or more of the following: a nanopore volume in the 6 nm to 11 nm range of 0.5 to 0.9 cc/g, a total nanopore volume in the 2 to 50 nm of 0.7 to 1.2 cc/g, a particle density of 0.7 to 0.9 g/cc; or the base extrudate is formed using an amorphous silica alumina support having a nanopore volume in the 6 nm to 11 nm range of 0.6 to 0.9 cc/g; and impregnating the base extrudate with at least one metal selected from the group consisting of elements from Group 6 and Groups 8 through 10 of the Periodic Table. 9. The method of claim 8 , wherein the base extrudate is formed using an alumina having a nanopore volume in the 6 nm to 11 nm range of 0.1 to 0.3 cc/g. 10. The method of claim 9 , wherein the base extrudate is formed using an amorphous silica alumina support having a nanopore volume in the 6 nm to 11 nm range of 0.6 to 0.9 cc/g. 11. The method of claim 8 , wherein the base extrudate is formed using an amorphous silica alumina support having a nanopore volume in the 6 nm to 11 nm range of 0.6 to 0.9 cc/g. 12. The method of claim 8 , wherein the base extrudate has a total nanopore volume in the 2 to 50 nm of 0.7 to 1.2 cc/g. 13. The method of claim 8 , wherein the base extrudate has a particle density of 0.7 to 0.9 g/cc. 14. A process for hydrocracking a hydrocarbonaceous feedstock, comprising contacting the feedstock with a hydrocracking catalyst under hydrocracking conditions to produce a hydrocracked effluent; the hydrocracking catalyst comprising a base extrudate comprising at least one molecular sieve, an alumina and an amorphous silica alumina support, wherein the base extrudate has one or more of the following: a nanopore volume in the 6 nm to 11 nm range of 0.5 to 0.9 cc/g, a total nanopore volume in the 2 to 50 nm of 0.7 to 1.2 cc/g, a particle density of 0.7 to 0.9 g/cc; or the base extrudate is formed using an amorphous silica alumina support having a nanopore volume in the 6 nm to 11 nm range of 0.6 to 0.9 cc/g; and at least one metal selected from the group consisting of elements from Group 6 and Groups 8 through 10 of the Periodic Table. 15. The process of claim 14 , wherein the base extrudate is formed using an alumina having a nanopore volume in the 6 nm to 11 nm range of 0.1 to 0.3 cc/g. 16. The process of claim 15 , wherein the base extrudate is formed using an amorphous silica alumina support having a nanopore volume in the 6 nm to 11 nm range of 0.6 to 0.9 cc/g. 17. The process of claim 14 , wherein the base extrudate is formed using an amorphous silica alumina support having a nanopore volume in the 6 nm to 11 nm range of 0.6 to 0.9 cc/g. 18. The process of claim 14 , wherein the base extrudate has a nanopore volume in the 6 nm to 11 nm range of 0.5 to 0.9 cc/g. 19. The process of claim 14 , wherein the base extrudate has a particle density of 0.7 to 0.9 g/cc. 20. The process of claim 14 , wherein the base extrudate has a nanopore volume in the 6 nm to 11 nm range of 0.6 to 0.9 cc/g.
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