Pipeline arrangement for utilizing a gas comprising biomethane
US-9222048-B1 · Dec 29, 2015 · US
US9790138B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9790138-B2 |
| Application number | US-201514831723-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 20, 2015 |
| Priority date | Sep 1, 2014 |
| Publication date | Oct 17, 2017 |
| Grant date | Oct 17, 2017 |
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Provided herein are methods of processing polyester-containing feedstocks to provide hydrocarbon products. Exemplary feedstocks include those containing estolide compounds, which may be processed under thermal and/or catalytic conditions to provide at least one hydrocarbon product.
Opening claim text (preview).
The invention claimed is: 1. A method comprising: providing a feedstock comprising at least one estolide compound; and converting the at least one estolide compound into at least one hydrocarbon product, wherein the at least one estolide compound is selected from compounds of the following formula: wherein x is, independently for each occurrence, an integer selected from 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, and 20; y is, independently for each occurrence, an integer selected from 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, and 20; n is an integer selected from 0 to 20; R 1 is an optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched; and R 2 is selected from hydrogen and an optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched; wherein each fatty acid chain residue of said at least one estolide compound is independently optionally substituted. 2. The method according to claim 1 , wherein converting the at least one estolide compound comprises deoxygenating the at least one estolide compound. 3. The method according to claim 2 , wherein the deoxygenating comprises decarboxylation. 4. The method according to claim 2 , wherein the deoxygenating comprises thermal decarboxylation. 5. The method according to claim 2 , wherein the deoxygenating comprises decarbonylation. 6. The method according to claim 2 , wherein the deoxygenating comprises hydrodeoxygenation. 7. The method according to claim 2 , wherein converting the at least one estolide compound is conducted in the presence of water. 8. The method according to claim 2 , wherein converting the at least one estolide compound is conducted in the presence of hydrogen. 9. The method according to claim 2 , wherein converting the at least one estolide compound comprises contacting said at least one estolide compound with at least one catalyst. 10. The method according to claim 9 , wherein the at least one catalyst comprises a transition metal. 11. The method according claim 2 , wherein converting the at least one estolide compound is conducted at a temperature of at least 100° C. 12. The method according to claim 11 , wherein converting the at least one estolide compound is conducted at a temperature of about 200° C. to about 500° C. 13. The method according to claim 2 , wherein converting the at least one estolide compound is conducted at a pressure greater than 1 atm absolute. 14. The method according to claim 2 , wherein the at least one hydrocarbon product comprises a C 10 to C 20 hydrocarbon. 15. The method according to claim 14 , wherein the at least one hydrocarbon product comprises a C 17 hydrocarbon and/or a C 18 hydrocarbon. 16. The method according to claim 1 , wherein the at least one hydrocarbon product undergoes further processing to provide at least one second hydrocarbon product. 17. The method according to claim 16 , wherein the further processing comprises cracking, hydrogenation and/or isomerization. 18. The method according to claim 17 , wherein the at least one second hydrocarbon product comprises a branched or unbranched C 4 to C 10 hydrocarbon. 19. The method according to claim 1 , wherein the feedstock further comprises at least one additional component. 20. The method according to claim 19 , wherein the at least one additional component comprises one or more of a Group I base oil, a Group II base oil, a Group III base oil, and a polyalphaolefin.
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by isomerisation (with simultaneous hydrogenation C07C5/13; with simultaneous dehydrogenation C07C5/373) · CPC title
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by cracking a single hydrocarbon or a mixture of individually defined hydrocarbons or a normally gaseous hydrocarbon fraction · CPC title
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