Lubricant basestock production with enhanced aromatic saturation
US-2018105761-A1 · Apr 19, 2018 · US
US11352579B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11352579-B2 |
| Application number | US-201816221742-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 17, 2018 |
| Priority date | Dec 21, 2017 |
| Publication date | Jun 7, 2022 |
| Grant date | Jun 7, 2022 |
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Disclosed are Group III base stocks comprising at least 30 wt % naphthenes, a viscosity index from 120 to 145; and a unique ratio of molecules with multi-ring naphthenes to single ring naphthenes (2R+N/1RN). A method for preparing the base stocks is also disclosed. Also disclosed is a lubricating oil having the base stock as a major component, and an additive as a minor component.
Opening claim text (preview).
The invention claimed is: 1. A Group III base stock comprising: at least about 30 wt % of naphthenes; about 30 wt % to about 70 wt % paraffins; wherein the Group III base stock has a viscosity index of about 120 to about 133; wherein the Group III base stock has a kinematic viscosity at 40° C. (KV40) of about 18.07 cSt to about 19.89 cSt; and wherein the Group III base stock has a ratio of molecules with multi-ring naphthenes to single ring naphthenes, 2R+N/1RN, of less than about 0.46. 2. The base stock of claim 1 , wherein the base stock has an amount of saturated hydrocarbons of at least 95 wt %. 3. The base stock of claim 1 , wherein the base stock has a kinematic viscosity at 100° C. (KV100) of about 4.0 cSt to about 5.0 cSt. 4. The base stock of claim 1 , wherein the base stock has a kinematic viscosity at 100° C. (KV100) of about 5.0 cSt to about 12.0 cSt. 5. The base stock of claim 4 , wherein the base stock has a viscosity index of about 20 to about 133. 6. A lubricating composition comprising the base stock of claim 1 and an additive. 7. The lubricating composition of claim 6 , wherein the base stock has a viscosity index of about 120 to about 133. 8. A method for producing a diesel fuel and a base stock, comprising: providing a feed stock comprising a vacuum gas oil; hydrotreating the feed stock under first effective hydrotreating conditions to produce a first hydrotreated effluent; hydrotreating the first hydrotreated effluent under second effective hydrotreating conditions to produce a second hydrotreated effluent; fractionating the second hydrotreated effluent to produce at least a first diesel product fraction and a bottoms fraction; hydrocracking the bottoms fraction under effective hydrocracking conditions to produce a hydrocracked effluent; dewaxing the hydrocracked effluent under effective catalytic dewaxing conditions to produce a dewaxed effluent, the dewaxing catalyst including at least one non-dealuminated, unidimensional, 10-member ring pore zeolite, and at least one Group 6 metal, Group 8 metal or combination thereof; hydrotreating the dewaxed effluent under third effective hydrotreating conditions to produce a third hydrotreated effluent; and fractionating the third hydrotreated effluent to form at least a second diesel product fraction and the base stock of claim 1 . 9. The method of claim 8 , wherein the feedstock has a solvent dewaxed oil feed viscosity index of about 45 to about 150. 10. The method of claim 8 , wherein the effective hydrotreating conditions include a temperature of about 300° C. to about 450° C., hydrogen partial pressure of about 1500 psi to about 5000 psi (˜10.3 MPa to ˜34.6 MPa), a liquid hourly space velocity of about 0.2 to about 10 hr −1 , and a hydrogen circulation rate of about 35.6 to about 1781 m 3 /m 3 (about 200 scf/bbl to about 10,000 scf/bbl). 11. The method of claim 8 , wherein the effective hydrocracking conditions include a temperature of about 288° C. to about 450° C., a hydrogen partial pressure of about 1000 psig to about 5000 psig about 6.9 MPa to about 34.6 MPa), a liquid hourly space velocity of about 0.05 h −1 to about 10 h −1 , and a hydrogen treat gas rate of about 35.6 m 3 /m 3 to about 1781 m 3 /m 3 (about 200 scf/bbl to about 10,000 scf/bbl). 12. The method of claim 8 , wherein the dewaxing catalyst comprises a molecular sieve having a SiO 2 :Al 2 O 3 ratio of about 200:1 to about 30:1 and comprises about 0.1 wt. % to about 3.33 wt. % framework Al 2 O 3 content, the dewaxing catalyst including about 0.1 wt. % to about 5 wt. % platinum. 13. The method of claim 12 , wherein the molecular sieve is EU-1, ZSM-35, ZSM-11, ZSM-57, NU-87, ZSM-22, EU-2, EU-11, ZBM-30, ZSM-48, ZSM-23, or a combination thereof. 14. The method of claim 13 , wherein the molecular sieve is ZSM-48, ZSM-23, or a combination thereof. 15. The method of claim 9 , wherein the dewaxing catalyst comprises at least one metal oxide, refractory binder, the binder being silica, alumina, titania, zirconia, or silica-alumina. 16. The method of claim 15 , wherein the metal oxide, refractory binder further comprises a second metal oxide, refractory binder different from the first metal oxide, refractory binder. 17. The method of claim 16 , wherein the dewaxing catalyst comprises a micropore surface area to total surface area ratio of greater than or equal to about 25%, wherein the total surface area equals the surface area of the external zeolite plus the surface area of the binder, the surface area of the binder being about 100 m 2 /g or less. 18. The method of claim 17 , wherein the hydrocracking catalyst is a zeolite Y based catalyst. 19. The method of claim 18 , wherein the effective dewaxing conditions include a temperature of about 200° C. to about 450° C., a hydrogen partial pressure of about 250 to about 5000 psi (about 1.8 MPa to 34.6 about MPa), a liquid hourly space velocity of about 0.2 to about 10 hr −1 , and a hydrogen circulation rate of about 35.6 m 3 /m 3 to about 1781 m 3 /m 3 (about 200 scf/bbl to about 10,000 scf/bbl). 20. The method of claim 8 , wherein the total conversion of the hydrocracked, dewaxed bottoms relative to the feedstock is about 30% to about 90%. 21. The method of claim 8 , wherein the feed stock is a solvent dewaxed oil. 22. A Group III base stock comprising: at least about 30 wt % of naphthenes; about 30 wt % to about 70 wt % paraffins; wherein the Group III base stock has: a viscosity index of 120 to 145; a kinematic viscosity at 40° C. (KV40) of about 18.07 cSt to about 19.89 cSt; and, a ratio of molecules with multi-ring naphthenes to single ring naphthenes, 2R+N/1RN, of less than about 0.46. 23. The base stock of claim 22 , wherein the base stock has a pour point of about −10° C. to about −30° C., a Noack volatility of about 0.5 wt. % to about 20 wt. %, and a cold crank simulator (CCS) value at −35° C. of about 100 cP up to about 70,000 cP. 24. A Group III base stock comprising: at least about 30 wt % of naphthenes; and about 30 wt % to about 70 wt % paraffins; wherein the Group III base stock has: a viscosity index of about 120 to about 145; a ratio of molecules with multi-ring naphthenes to single ring naphthenes, 2R+N/1RN, of less than about 0.46; a kinematic viscosity at 100° C. (KV100) of about 8 cSt to about 12 cSt; a kinematic viscosity at 40° C. (KV40) of about 53.35 cSt to about 59.7 cSt; and a cold crank simulator (CCS) value at −35° C. of about 10,000 cP to about 70,000 cP. 25. The base stock of claim 24 , wherein the base stock has a pour point of about −10° C. to about −30° C., and a Noack volatility is about 0.5 wt. % to about 20 wt. %. 26. The base stock of claim 1 , wherein the base stock has a KV40 of about 18.07 cSt to about 19 cSt. 27. The base stock of claim 1 , wherein the base stock has a KV40 of about 19 cSt to about 19.89 cSt. 28. The base stovk of claim 24 , wherein the base stock has a weight ratio of molecules with multi-ring naphthenes to single ring naphthenes, 2R+N/1RN, of about 0.36 about 0.4.
including cracking steps and other hydrotreatment steps · CPC title
containing platinum group metals or compounds thereof · CPC title
the catalyst containing platinum group metals or compounds thereof · CPC title
Diesel oil · CPC title
Gasoil · CPC title
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