Compositions comprising estolide compounds and methods of making and using the same
US-9016097-B2 · Apr 28, 2015 · US
US9228146B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9228146-B2 |
| Application number | US-201514613311-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 3, 2015 |
| Priority date | Aug 31, 2010 |
| Publication date | Jan 5, 2016 |
| Grant date | Jan 5, 2016 |
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.
Provided herein are compounds of the formula: in which n is an integer equal to or greater than 1; R 2 is selected from hydrogen and optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched; and R 1 , R 3 , and R 4 , independently for each occurrence, are selected from optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched, wherein compositions comprising the compounds are characterized by particular combinations of values for estolide number, kinematic viscosity, and pour point. Also provided are compositions containing the compounds and methods of making both the compounds and compositions thereof.
Opening claim text (preview).
The invention claimed is: 1. A composition consisting essentially of at least one estolide compound, said composition having: an EN that is an integer or fraction of an integer selected from 1.0 to 1.6, wherein the EN is the average number of estolide linkages in compounds according to Formula I; and a kinematic viscosity of about 4 cSt to about 10 cSt when measured at 100° C., wherein said at least one estolide compound is selected from compounds of Formula I: wherein x is, independently for each occurrence, an integer selected from 7 and 8; y is, independently for each occurrence, an integer selected from 0, 1, and 2; n is an integer selected from 0 to 4; R 1 is an unsubstituted C 7 to C 17 alkyl that is saturated and branched or unbranched; and R 2 is an unsubstituted C 1 to C 18 alkyl that is saturated or unsaturated, and branched or unbranched, wherein each fatty acid chain residue of said at least one estolide compound is unsubstituted. 2. The composition according to claim 1 , wherein x+y is 7 for each fatty acid chain residue. 3. The composition according to claim 1 , wherein x+y is 8 for each fatty acid chain residue. 4. The composition according to claim 1 , wherein R 2 is selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decanyl, undecanyl, dodecanyl, tridecanyl, tetradecanyl, pentadecanyl, hexadecanyl, heptadecanyl, and octadecanyl, which are saturated and branched or unbranched. 5. The composition according to claim 1 , wherein R 2 is selected from C 6 to C 12 alkyl that is branched. 6. The composition according to claim 5 , wherein R 2 is 2-ethylhexyl. 7. The composition according to claim 1 , wherein R 1 is selected from C 7 alkyl that is saturated and unbranched. 8. The composition according to claim 1 , wherein R 1 is selected from C 9 alkyl that is saturated and unbranched. 9. The composition according to claim 1 , wherein R 1 is selected from C 10 alkyl that is saturated and unbranched. 10. The composition according to claim 1 , wherein said composition has a kinematic viscosity of about 15 cSt when measured at 40° C. 11. The composition according to claim 1 , wherein said composition has a kinematic viscosity of about 16 cSt when measured at 40° C. 12. The composition according to claim 1 , wherein said composition exhibits an iodine value (IV) of less than 10 cg/g. 13. The composition according to claim 10 , wherein said composition exhibits an iodine value (IV) of less than 5 cg/g. 14. The composition according to claim 1 , wherein said at least one estolide compound is derived from a process that comprises forming a covalent bond between an oxygen of a carboxylic group of at least one first fatty acid and a carbon of at least one site of unsaturation of at least one second fatty acid. 15. The composition according to claim 2 , wherein R 1 is selected from C 9 alkyl that is saturated and unbranched. 16. The composition according to claim 15 , wherein said composition has a kinematic viscosity of about 15 cSt when measured at 40° C. 17. The composition according to claim 3 , wherein R 1 is selected from C 10 alkyl that is saturated and unbranched. 18. The composition according to claim 17 , wherein said composition has a kinematic viscosity of about 16 cSt when measured at 40° C. 19. The composition according to claim 1 , wherein said composition exhibits a pour point of less than −50° C. 20. The composition according to claim 1 , wherein said composition exhibits a pour point of −50° C. to −60° C.
Environmental friendly compositions · CPC title
Gate valves; Sliding valves; Cocks · CPC title
used as base material · CPC title
Selective reciprocation or rotation · CPC title
with fatty acids · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.