Hydrocracking catalyst for hydrocarbon oil, method for producing hydrocracking catalyst, and method for hydrocracking hydrocarbon oil with hydrocracking catalyst
US-10081009-B2 · Sep 25, 2018 · US
US10357761B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10357761-B2 |
| Application number | US-201514719582-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 22, 2015 |
| Priority date | May 22, 2014 |
| Publication date | Jul 23, 2019 |
| Grant date | Jul 23, 2019 |
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The present invention relates to a catalyst for fluidized catalytic cracking of hydrocarbon oil containing a framework-substituted zeolite-1 in which zirconium atoms and/or hafnium atoms form a part of a framework of an ultra-stable Y-type zeolite.
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We claim: 1. A method for cracking a hydrocarbon oil comprising contacting the hydrocarbon oil with a catalyst comprising an ultra-stable Y-type zeolite in a fluidized catalytic cracking unit to produce light olefins and gasoline fuel, wherein the ultra-stable Y-type zeolite is a framework-substituted zeolite in which a part of aluminum atoms constituting a zeolite framework thereof is substituted with 0.1-5 mass % zirconium atoms and 0.1-5 mass % titanium ions calculated on an oxide basis. 2. The method according to claim 1 , comprising contacting a hydrocarbon oil having a boiling point range above about 350° C. to said catalyst at a reaction temperature ranging from about 450° C. to about 700° C., a pressure of about 1 to about 10 bars, for from about 0.1 to about 60 seconds, at a catalyst to oil ratio of from about 2:1 to about 30:1. 3. The method according to claim 1 , wherein the fluidized catalytic cracking unit is a downer reactor. 4. The method according to claim 1 , wherein the fluidized catalytic cracking unit is a riser reactor. 5. The method according to claim 1 , comprising carrying out said cracking under conditions effective to maximize production of gasoline and light olefins. 6. The method according to claim 1 , comprising carrying out said cracking under conditions effective to maximize production of light olefins. 7. The method according to claim 1 , wherein said catalyst comprises a mixture of said framework-substituted ultra-stable Y-type zeolite and one or more additional fluidized cracking catalyst materials. 8. The method according to claim 1 , wherein the framework-substituted ultra-stable Y-type zeolite has a crystal lattice constant of 2.430 to 2.450 nm, a specific surface area of about 600 to about 900 m 2 /g, and a molar ratio of SiO 2 to Al 2 O 3 in the range of about 5:1 to about 100:1. 9. The method of claim 1 , wherein said catalyst comprises from 20% to 50% by mass of zeolite. 10. The method of claim 1 , wherein said catalyst comprises from 15% to 25% by mass of inorganic binder. 11. The method of claim 10 , wherein said inorganic binder is silica sol, water glass, or silicic acid liquid. 12. The method of claim 10 , wherein said inorganic binder is basic aluminum chloride, aluminum biphosphate, or alumina sol. 13. The method of claim 10 , wherein said inorganic binder comprises kaolin, clay, activated alumina, porous silica, a rare earth oxide, or a metal trapping agent. 14. The method of claim 13 , wherein said rare earth oxide has formula RE 2 O 3 and is present at a range of 0 to 3% by mass. 15. The method of claim 14 , wherein RE is Ce, La, Pr, or Nd. 16. The method of claim 1 , wherein the ultra-stable Y-type zeolite has a molar ratio of SiO 2 to Al 2 O 3 in the range of about 20:1 to 100:1. 17. The method of claim 16 , wherein the ultra-stable Y-type zeolite has a molar ratio of SiO 2 to Al 2 O 3 in the range of about 25:1 to 80:1.
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