Friction modifier and lubricating oil composition
US-2015376538-A1 · Dec 31, 2015 · US
US10227539B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10227539-B2 |
| Application number | US-201615198346-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 30, 2016 |
| Priority date | Jun 9, 2014 |
| Publication date | Mar 12, 2019 |
| Grant date | Mar 12, 2019 |
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Methods are provided for modifying hydrogenation catalysts having silica supports (or other non-alumina supports) with additional alumina, and using such catalysts to achieve unexpectedly superior hydrogenation of feedstocks. The modified hydrogenation catalysts can have a relatively low cracking activity while providing an increased activity for hydrogenation.
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What is claimed is: 1. A method for forming a lubricant boiling range product, comprising: exposing a 600° F.+ (316° C.+) portion of a hydrocracked effluent to a supported catalyst under effective hydrogenation conditions to form a hydrogenated effluent, the supported catalyst comprising 0.1 wt % to 5.0 wt % of a Group VIII noble metal on a silica support, the supported catalyst further comprising 0.3 wt % to 2.5 wt % alumina deposited on the silica support, the supported catalyst having a ratio of aluminum atoms in tetrahedral sites to octahedral sites of at least 1.0, the supported catalyst having a relative acidity of less than 1 when measured using the 2MP2 Isomerization Test, wherein less than 3 wt % of the molecules in the hydrocracked effluent boiling above 700° F. are converted to molecules boiling below 700° F. in the hydrocracked effluent when measured at a reaction temperature of 354° C.; dewaxing the hydrogenated effluent under catalytic dewaxing conditions to form a dewaxed effluent; and hydrofinishing at least a portion of the dewaxed effluent under hydrofinishing conditions to form a hydrofinished effluent comprising a lubricant boiling range product. 2. The method of claim 1 , further comprising exposing a feedstock comprising a lubricant boiling range portion to a hydrocracking catalyst under hydrocracking conditions to form the hydrocracked effluent; and separating the hydrocracked effluent to form a fraction comprising the 600° F.+ (316° C.+) portion of the hydrocracked effluent. 3. The method of claim 2 , wherein the feedstock comprises a hydrotreated feedstock. 4. The method of claim 3 , wherein the hydrotreated feedstock comprises a hydrotreated effluent, the hydrotreated effluent being cascaded to the hydrocracking catalyst without intermediate separation. 5. The method of claim 1 , wherein the 600° F.+ (316° C.+) portion of the hydrocracked effluent comprises 50 wppm or less of sulfur. 6. The method of claim 1 , wherein the catalyst comprises 0.3 wt % to 2.1 wt % alumina deposited on the silica support. 7. The method of claim 1 , wherein the catalyst comprises 0.5 wt % to 2.2 wt % alumina deposited on the silica support. 8. The method of claim 1 , wherein the effective hydrogenation conditions comprise a temperature from 75° C. to 425° C.; a hydrogen partial pressure from 100 psig (0.7MPa) to 3000 psig (20.7 MPa); a liquid hourly space velocity from 0.1 hr −1 to 5 hr −1 LHSV; and a hydrogen treat gas rate of from 35.6 m 3 /m 3 to 1781 m 3 /m 3 (200 SCF/B to 10,000 SCF/B). 9. The method of claim 1 , wherein the Group VIII noble metal comprises Pt. 10. The method of claim 9 , wherein the Group VIII noble metal further comprises one or more of Pd, Ir, or Rh, a molar ratio of Pt to the one or more of Pd, Ir, or Rh being at least 1: 1. 11. The method of claim 9 , wherein the supported catalyst comprises 0.1 wt % to 2.0 wt % of the Group VIII noble metal. 12. The method of claim 1 , wherein the ratio of aluminum atoms in tetrahedral sites to octahedral sites is at least 1.5.
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