ZSM-5, its preparation and use in ethylbenzene dealkylation
US-10427143-B2 · Oct 1, 2019 · US
US11078431B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11078431-B2 |
| Application number | US-201916715555-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 16, 2019 |
| Priority date | Dec 16, 2019 |
| Publication date | Aug 3, 2021 |
| Grant date | Aug 3, 2021 |
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The present disclosure relates to a process for the deolefinization of hydrocarbon streams through an aromatic alkylation reaction by olefins, using a catalyst containing a framework-substituted zirconium and/or titanium and/or hafnium-modified ultra-stable Y (USY) type zeolite.
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What is claimed is: 1. A process for deolefinization of a hydrocarbon feed containing aromatic compounds and olefins, the process comprising the step of contacting the hydrocarbon feed with a catalyst containing a framework-substituted ultra-stable Y (USY)-type zeolite in which a portion of aluminum atoms constituting a zeolite framework thereof is substituted with zirconium atoms and/or titanium and/or hafnium atoms, wherein the olefins alkylate the aromatic compounds in the hydrocarbon feed, thereby producing a deolefinated hydrocarbon product. 2. The process according to claim 1 , wherein the framework-substituted USY-type zeolite in the catalyst comprises zirconium atoms and titanium atoms. 3. The process according to claim 1 , wherein the framework-substituted USY-type zeolite in the catalyst comprises from about 0.1 to about 5% by mass zirconium and/or titanium and/or hafnium atoms, each calculated as the oxide basis. 4. The process according to claim 1 , wherein the framework-substituted USY-type zeolite in the catalyst further includes a support comprising inorganic oxides selected from the group consisting of alumina, silica-alumina and combinations thereof. 5. The process according to claim 1 , wherein the hydrocarbon feed comprises an aromatic rich hydrocarbon oil having a boiling point range of about 15° C. to about 500° C. 6. The process according to claim 1 , wherein the contacting is operated at reaction temperature range of about 50° C. to about 250° C., a pressure of about 1 to about 30 bars and a liquid hourly space velocity (LHSV) of about 0.5 to about 50 h −1 . 7. The process according to claim 1 , wherein the deolefinated product contains less than about 500 ppm sulfur. 8. The process according to claim 1 , wherein the deolefinated hydrocarbon product containing less than about 100 ppm nitrogen. 9. The process according to claim 1 , wherein the hydrocarbon feed contains greater than about 1 wt % olefins. 10. The process according to claim 1 , wherein the deolefinated hydrocarbon product contains less than about 10 wt % olefins. 11. The process according to claim 1 , wherein the hydrocarbon feed is deolefinated at least about 95 wt %. 12. The process according to claim 1 , wherein the deolefinated hydrocarbon product has bromine index less than about 60,000. 13. The process according to claim 1 , wherein the aromatic compounds in the hydrocarbon feed contains benzene and alkylated benzenes. 14. The process according to claim 13 , wherein the aromatic compounds in the hydrocarbon feed comprise C6 to C10 aromatic compounds. 15. The process according to claim 1 , wherein the deolefinated hydrocarbon product comprises less olefin hydrocarbons and more alkylated aromatic compounds as compared with the hydrocarbon feed. 16. The process according to claim 1 , wherein the hydrocarbon feed is fluid catalytic cracking (FCC) naphtha, coking naphtha or other naphtha coming from the cracking units in which no hydrogen is used. 17. The process according to claim 1 , wherein the catalyst further includes an active metal selected from the group consisting of IUPAC Group 7 to 11 metal of the Periodic Table. 18. The process according to claim 1 , wherein the deolefinated product contains less than about 10 ppm sulfur. 19. The process according to claim 1 , wherein the deolefinated product contains less than about 0.5 ppm sulfur. 20. The process according to claim 1 , wherein the deolefinated hydrocarbon product containing less than about 10 ppm nitrogen. 21. The process according to claim 1 , wherein the deolefinated hydrocarbon product containing less than about 0.5 ppm nitrogen. 22. The process according to claim 1 , wherein the deolefinated hydrocarbon product contains less than about 1 wt % olefins. 23. The process according to claim 1 , wherein the deolefinated hydrocarbon product contains less than about 0.5 wt % olefins. 24. The process according to claim 1 , wherein the hydrocarbon feed is deolefinated at least about 99 wt %. 25. The process according to claim 1 , wherein the hydrocarbon feed is deolefinated at least about 99.99 wt %. 26. The process according to claim 1 , wherein the deolefinated hydrocarbon product has bromine index less than about 10,000. 27. The process according to claim 1 , wherein the deolefinated hydrocarbon product has bromine index less than about 1,000. 28. A process for alkylating aromatic compounds in a hydrocarbon feed containing aromatic compounds and olefins, the process comprising the step of contacting the hydrocarbon feed with a catalyst containing framework-substituted ultra-stable Y (USY)-type zeolite in which a portion of aluminum atoms constituting a zeolite framework thereof is substituted with zirconium atoms and/or titanium and/or hafnium atoms, wherein the olefins alkylate the aromatic compounds in the hydrocarbon feed, thereby producing alkylated aromatic compounds.
Controlling or regulating of reforming operations · CPC title
containing crystalline zeolitic molecular sieves, other than aluminosilicates · CPC title
Organic compounds not containing metal atoms · CPC title
containing arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium · CPC title
of the faujasite type, e.g. type X or Y · CPC title
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