Alcohol composition and derivatives thereof
US-2017175026-A1 · Jun 22, 2017 · US
US11932819B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11932819-B2 |
| Application number | US-201917291134-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 28, 2019 |
| Priority date | Nov 5, 2018 |
| Publication date | Mar 19, 2024 |
| Grant date | Mar 19, 2024 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention relates to a lubricant comprising a diester of adipic acid with a tridecanol mixture which comprises 20 to 60% of at least triply branched tridecanols, 10 to 50% doubly branched tridecanols, and 5 to 30% singly branched and/or linear tridecanols, and where the percentages are determined by gas chromatography.
Opening claim text (preview).
The invention claimed is: 1. A method for reducing friction between moving surfaces comprising the steps of: a) obtaining a tridecanol mixture by hydroformylation and hydrogenation of a mixture of isomeric dodecenes obtained by reacting a hydrocarbon mixture comprising butenes on a heterogeneous catalyst, wherein the heterogeneous catalyst comprises nickel oxide, and wherein the heterogeneous catalyst is a precipitation catalyst obtained by mixing aqueous solutions of nickel salts and silicates; wherein the tridecanol mixture comprises 20 to 60% of at least triply branched tridecanols, 10 to 50% doubly branched tridecanols, and 5 to 30% singly branched and/or linear tridecanols, and where the percentages are determined by gas chromatography; where the tridecanol mixture comprises less than 5 wt % tetradecanol; b) obtaining a diester of adipic acid with the tridecanol mixture by esterification of adipic acid and the tridecanol mixture, wherein the diester has a pour point below −50° C. and a viscosity index of at least 140; and c) contacting the surfaces with a lubricant comprising the diester of the adipic acid with the tridecanol mixture. 2. The method according to claim 1 where the tridecanol mixture comprises 25 to 50% of at least triply branched tridecanols. 3. The method according to claim 1 where the tridecanol mixture comprises 20 to 45% doubly branched tridecanols. 4. The method according to claim 1 where the tridecanol mixture comprises 10 to 25% singly branched and/or linear tridecanols. 5. The method according to claim 1 where the tridecanol mixture comprises at least 85 wt % of linear or branched tridecanols. 6. The method according to claim 5 where the tridecanol mixture comprises at least 98 wt % of linear or branched tridecanols. 7. The method according to claim 1 where the tridecanol mixture comprises less than 15 wt % dodecanol. 8. The method according to claim 7 where the tridecanol mixture comprises less than 2 wt % dodecanol. 9. The method according to claim 1 where the tridecanol mixture comprises less than 1 wt % tetradecanol. 10. The method according to claim 5 , wherein the tridecanol mixture comprises at least 98 wt % of linear or branched tridecanols, the tridecanol mixture comprises less than 2 wt % dodecanol and the tridecanol mixture comprises less than 1 wt % tetradecanol. 11. The method according to claim 1 further comprising a base oil selected from the group consisting of mineral oils, polyalphaolefins, polymerized and interpolymerized olefins, alkyl naphthalenes, alkylene oxide polymers, silicone oils, phophate ester and carboxylic acid ester; and further comprises a lubricant additive. 12. The method according to claim 1 , where the tridecanol mixture comprises less than 3 wt % tetradecanol. 13. The method according to claim 1 , wherein the heterogeneous catalyst is a catalyst whose active substantial constituents are from 10 to 70 percent by weight of nickel oxide, from 5 to 30 percent by weight of titanium dioxide and/or zirconium dioxide, and from 0 to 20 percent by weight of aluminum oxide, and the remainder being silicon dioxide. 14. The method according to claim 1 , wherein the heterogeneous catalyst is obtainable by precipitating the catalyst composition at a pH of from 5 to 9 by adding an aqueous solution comprising nickel nitrate to an alkali metal water glass solution which comprises titanium dioxide and/or zirconium dioxide, filtering, drying and amlealing at from 350 to 650 degrees C. 15. The method according to claim 1 , wherein the diester has a pour point below −61° C. 16. The method according to claim 1 , wherein the diester has a viscosity index of at least 145. 17. The method according to claim 1 , wherein the nickel salt is nickel nitrate and the silicate is sodium silicate.
of polycarboxylic acids · CPC title
Mixtures of base-materials and additives · CPC title
Special methods of preparation of lubricating compositions; Chemical modification by after-treatment of components or of the whole of a lubricating composition, not covered by other classes · CPC title
used as base material · CPC title
used as base material · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.