Methods for making linear internal olefins from mixtures of linear and branched olefins
US-2024051900-A1 · Feb 15, 2024 · US
US9416068B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9416068-B2 |
| Application number | US-201213714542-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 14, 2012 |
| Priority date | Jun 16, 2010 |
| Publication date | Aug 16, 2016 |
| Grant date | Aug 16, 2016 |
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The invention relates to a method for producing liquid fuel having a high alkane content and a low oxygenized compound content, said method comprising at least: a first step of treating 2-methylfuran with a catalyst and water in reaction conditions in order to form a mixture of products with at least ten carbon atoms; and a second step of catalytic hydrogenation and dehydration of the product or the mixture obtained in step 1, using suitable hydrogenation and dehydration catalysts.
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The invention claimed is: 1. A method for producing fuel comprising: a) contacting 2-methylfuran with a catalyst and water under suitable reaction conditions to form a mixture of products comprising at least one oligomer of 2-methylfuran having at least ten carbon atoms, and b) catalytically hydrodeoxygenating said mixture of products to produce the fuel. 2. The method according to claim 1 , wherein the mixture of products is a mixture of oxygenated hydrocarbons. 3. The method according to claim 1 , wherein the at least one oligomer is present in an amount of at least 20% by weight. 4. The method according to claim 1 , wherein the mixture of products have at least 15 carbon atoms. 5. The method according to claim 1 , wherein the catalyst of step a) is an acid catalyst. 6. The method according to claim 5 , wherein the acid catalyst comprises a mineral acid. 7. The method according to claim 6 , wherein the mineral acid comprises sulfuric acid. 8. The method according to claim 5 , wherein step a) is carried out in the presence of an insoluble acid. 9. The method according to claim 5 , wherein step a) is carried out in the presence of an acid resin. 10. The method according to claim 1 , wherein the reaction of step a) is carried out at a temperature between 0° C. and 200° C. 11. The method according to claim 1 , wherein the hydrodeoxygenation is carried out at a temperature between 180° C. and 450° C. 12. The method according to claim 1 , wherein the hydrodeoxygenation is carried out at a hydrogen pressure between 0.1 bar and 60 bar. 13. The method according to claim 1 , wherein the hydrodeoxygenation catalyst comprises at least a metal function and a dehydrating function. 14. The method according to claim 13 , wherein the hydrodeoxygenation catalyst comprises at least one of the elements selected from Re, Pd, Ru, Pt, Rh, Ni, and Cu, and further comprises a support. 15. The method according to claim 14 , wherein the support is selected from active carbon, an inorganic oxide and combinations thereof. 16. The method according to claim 15 , wherein the support is an inorganic oxide selected from alumina, zirconia, titania, silica and combinations thereof. 17. The method according to claim 10 , wherein the reaction of step a) is carried out at a temperature between 0° C. and 100° C. 18. The method according to claim 11 , wherein the hydrodeoxygenation is carried out at a temperature between 220° C. and 400° C. 19. The method according to claim 12 , wherein the hydrodeoxygenation is carried out at a hydrogen pressure between 3 bar and 50 bar.
using bio-feedstock · CPC title
Biomass · CPC title
of vegetal origin · CPC title
characterised by the catalyst used · CPC title
polymerisation, e.g. oligomerisation · CPC title
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