An MCM-41 catalyst having a crystalline framework containing SiO2 and a Group IV metal oxide, such as TiO2 or ZrO2 is provided. The catalyst is low in acidity and is suitable for use in processes involving aromatic saturation of hydrocarbon feedstocks.
대표청구항▼
1. An aromatics hydrogenation process for a hydrocarbon feedstream comprising: a) contacting a hydrocarbon feedstream that contains aromatics with a hydrogenation catalyst in the presence of a hydrogen-containing treat gas in a first reaction stage operated under effective aromatics hydrogenation co
1. An aromatics hydrogenation process for a hydrocarbon feedstream comprising: a) contacting a hydrocarbon feedstream that contains aromatics with a hydrogenation catalyst in the presence of a hydrogen-containing treat gas in a first reaction stage operated under effective aromatics hydrogenation conditions, the effective aromatics hydrogenation conditions comprising a temperature of about 190° C. or less, wherein said hydrogenation catalyst comprises: i) an inorganic porous crystalline phase material comprising MCM-41 and having, after calcination, a hexagonal arrangement of uniformly-sized pores having diameter of at least about 15 Angstroms to about 25 Angstroms and exhibiting a hexagonal diffraction pattern that can be indexed with a d100 value greater than about 18 Angstroms, wherein the inorganic porous crystalline phase material contains SiO2 and XO2, where X is selected from Ti, Zr, or a combination thereof, and the inorganic porous crystalline phase material is formed from a synthesis mixture having a ratio of SiO2:XO2 of about 100:1 or less, and(ii) at least one hydrogenation-dehydrogenation component selected from the Group VIII noble metals. 2. The process of claim 1, wherein the inorganic porous crystalline phase material is MCM-41. 3. The process of claim 2, wherein the Group VIII noble metal is Pt, Pd, Ir, Rh, or a combination thereof. 4. The process according to claim 2, wherein the ratio of SiO2:XO2 in the synthesis mixture for forming the inorganic porous crystalline phase material is from about 7.5:1 to about 100:1. 5. The process according to claim 2, wherein said hydrogenation catalyst further comprises a binder material selected from active and inactive materials, inorganic materials, clays, alumina, silica, silica-alumina, titania, zirconia, or a combination thereof. 6. The process according to claim 5 wherein said binder material is selected from silica-alumina, alumina, titania, or zirconia. 7. The process according to claim 2, wherein the hydrocarbon feedstream is a hydrocarbon fluid, a diesel boiling range feedstream, or a lube oil boiling range feedstream. 8. The process according to claim 2, wherein said hydrogenation-dehydrogenation component is present in an amount ranging from about 0.1 to about 2.0 wt. %. 9. The process according to claim 8, wherein said hydrogenation-dehydrogenation component is selected from palladium, platinum, and mixtures thereof. 10. The process according to claim 1, wherein said hydrocarbon feedstream is derived from crude oils, shale oils and tar sands as well as synthetic feeds and is selected from hydrocarbon feedstreams having an initial boiling points of about 315° C. or higher. 11. The process according to claim 10 wherein said hydrocarbon feedstream contains up to 0.2 wt. % of nitrogen, up to 3.0 wt. % of sulfur, and up to about 50 wt. % aromatics, all based on the hydrocarbon feedstream. 12. The process according to claim 1 wherein said hydrocarbon feedstream has a sulfur content below about 500 wppm. 13. An aromatics hydrogenation process for hydrocarbon feedstreams comprising: a) contacting a hydrocarbon feedstream containing aromatics, nitrogen and organically bound sulfur contaminants in a first reaction stage operated under effective hydrotreating conditions and in the presence of hydrogen-containing treat gas with a hydrotreating catalyst comprising about at least one Group VIII metal oxide and at least one Group VI metal oxide thereby producing a reaction product comprising at least a vapor product and a liquid hydrocarbon product; andb) contacting said reaction product with a hydrogenation catalyst in the presence of a hydrogen-containing treat gas in a second reaction stage operated under effective aromatics hydrogenation conditions, the effective aromatics hydrogenation conditions comprising a temperature of about 190° C. or less, wherein said hydrogenation catalyst comprises: i) an MCM-41 support material having a crystalline framework that contains SiO2 and XO2, where X is selected from Ti, Zr, or a combination thereof, the MCM-41 support material being formed from a synthesis mixture having a ratio of SiO2:XO2 in the synthesis mixture of 100:1 or less; the support material having a hexagonal arrangement of uniformly-sized pores having diameter of about 15 Angstroms to about 25 Angstroms; andii) at least one hydrogenation-dehydrogenation component selected from the Group VIII noble metals. 14. The process according to claim 13 wherein said MCM-41 support material is composited with a binder material. 15. The process according to claim 14 wherein said binder material is selected from active and inactive materials, synthetic zeolites, naturally occurring zeolites, inorganic materials, clays, alumina, and silica-alumina. 16. The process according to claim 13 wherein said hydrogenation-dehydrogenation component is present in an amount ranging from about 0.1 to about 2.0 wt. %. 17. The process according to claim 13 wherein said hydrogenation-dehydrogenation component is selected from platinum, palladium, and mixtures thereof. 18. The process according to claim 13 wherein said process further comprises: a) separating said vapor product from said liquid hydrocarbon product; and b) conducting said liquid hydrocarbon product to the second reaction stage containing said hydrogenation catalyst. 19. A method for hydroprocessing a hydrocarbon feedstream comprising: a) contacting a hydrocarbon feedstream containing aromatics in a first reaction stage operated under effective catalytic dewaxing conditions and in the presence of hydrogen-containing treat gas with a dewaxing catalyst thereby producing a reaction product; andb) contacting said reaction product, the reaction product having a sulfur content of from about 210 wppm to about 500 wppm, with a hydrogenation catalyst in the presence of a hydrogen-containing treat gas in a second reaction stage operated under effective aromatics hydrogenation conditions, the effective aromatics hydrogenation conditions comprising a temperature of about 275° C. to about 400° C., wherein said hydrogenation catalyst comprises: i) an MCM-41 support material having a crystalline framework that contains SiO2 and XO2, where X is selected from Ti, Zr, or a combination thereof, the MCM-41 support material being formed from a synthesis mixture having a ratio of SiO2:XO2 in the synthesis mixture of 100:1 or less; the support material having a hexagonal arrangement of uniformly-sized pores having a diameter of 15 Angstroms to about 40 Angstroms; andii) at least one hydrogenation-dehydrogenation component selected from the Group VIII noble metals. 20. The method of claim 19, further comprising hydrotreating the hydrocarbon feedstream under effective hydrotreating conditions prior to contacting the hydrocarbon feedstream with the dewaxing catalyst. 21. The method of claim 19, further comprising hydrofinishing the hydrocarbon feedstream under effective hydrofinishing conditions prior to contacting the hydrocarbon feedstream with the dewaxing catalyst. 22. The method of claim 21, wherein hydrofinishing the hydrocarbon feedstream prior to contacting the hydrocarbon feedstream with the dewaxing catalyst comprises exposing the feedstream to a catalyst that comprises: i) an MCM-41 support material having a crystalline framework that contains SiO2 and XO2, where X is a Group IV metal, the MCM-41 support material being formed from a synthesis mixture having a ratio of SiO2:XO2 in the synthesis mixture of 100:1 or less; and ii) at least one hydrogenation-dehydrogenation component selected from the Group VIII noble metals.
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