Diesel-soluble lignin oils and methods of their production
US-2018002607-A1 · Jan 4, 2018 · US
US12054674B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12054674-B2 |
| Application number | US-202218083650-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 19, 2022 |
| Priority date | Dec 23, 2021 |
| Publication date | Aug 6, 2024 |
| Grant date | Aug 6, 2024 |
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The disclosure relates to a process for converting lignin ( 10 ) to renewable product ( 80 ), wherein the process comprises the following steps; mixing ( 100 ) lignin ( 10 ) with aqueous solution ( 20 ) to obtain a mixture ( 30 ); heating ( 110 ) the mixture ( 30 ) of step (a) to a temperature between 290 and 350° C., under a pressure from 70 to 165 bar, to obtain a first product mix ( 40 ); separating aqueous phase ( 53 ) and oil phase ( 50 ), and optionally gas ( 51 ) and solids ( 52 ), of the first product mix ( 40 ) of step (b); and heating ( 130 ) the oil phase ( 50 ) of step (c) and solvent ( 60 ) to obtain a second product mix ( 70 ). The second product mix ( 70 ) can be used as such, it can be directed to separation ( 140 ) or it can be upgraded. The obtained liquid renewable product is suitable as chemicals, fuel, fuel components or feedstock for fuel production.
Opening claim text (preview).
The invention claimed is: 1. A process for converting lignin ( 10 ) to renewable product ( 80 ), characterized in that the process comprises the following steps, (a) mixing ( 100 ) lignin ( 10 ) with aqueous solution ( 20 ), at atmospheric conditions or at a temperature lower than 100° C., for 1-60 minutes to obtain a mixture ( 30 ); (b) heating ( 110 ) the mixture ( 30 ) of step (a) at a temperature between 290 and 350° C., under a pressure from 70 to 165 bar, to obtain a first product mix ( 40 ); (c) separating ( 120 ) aqueous phase ( 53 ) and oil phase ( 50 ), and optionally gas ( 51 ) and/or solids ( 52 ), of the first product mix ( 40 ) of step (b); and (d) heating ( 130 ) the oil phase ( 50 ) of step (c) and solvent ( 60 ) at a temperature between 360° C. to 450° C., under a pressure from 1 to 120 bar. 2. The process according to claim 1 , characterized in that the aqueous solution ( 20 ) in step (a) is water or recirculated aqueous phase ( 53 ). 3. The process according to claim 1 , characterized in that the amount of lignin feedstock is 2-50 wt % of the total amount of lignin and aqueous solution by weight. 4. The process according to claim 1 , characterized in that said solvent ( 60 ) in step (d) is renewable hydrocarbons, oxygen containing hydrocarbons or mixtures thereof. 5. The process according to claim 1 , characterized in that the oil phase to solvent ratio in step (d) is from 1:5 to 1.5:1 by weight. 6. The process according to claim 1 , characterized in that the pH of the aqueous phase ( 53 ) is below pH 9. 7. The process according to claim 1 , characterized in that lignin ( 10 ) is kraft lignin separated from black liquor and the lignin comprises less than 10 wt % of impurities or residues from the black liquor. 8. The process according to claim 1 , characterized in that the lignin ( 10 ) comprises 15-98 wt % organics; 0.1-15 wt % ash; and/or 1.5-80 wt % water. 9. The process according to claim 1 , characterized in that the lignin ( 10 ) comprises below 40 wt %, oxygen daf (dry-ash-free). 10. The process according to claim 1 , characterized in that step (d) ( 130 ) is followed by a step (e) ( 140 ) comprising separating aqueous phase ( 83 ), oil phase ( 80 ) and optionally gas ( 81 ) and/or solids ( 82 ) of the second product mix ( 70 ) of step (d) ( 130 ). 11. The process according to claim 10 , characterized in that the oil phase ( 50 , 80 ) comprises below 25 wt % oxygen. 12. The process according to claim 1 , characterized in that step (d) ( 130 ) is followed by fractionation ( 200 ) to obtain a light fraction ( 90 ) and a heavy fraction ( 91 ) and optionally a bottom residue fraction ( 92 ) and/or a gaseous fraction. 13. The process according to claim 10 , characterized in that step (e) ( 140 ) is followed by fractionation ( 200 ) to obtain a light fraction ( 90 ) and a heavy fraction ( 91 ) and optionally a bottom residue fraction ( 92 ) and/or a gaseous fraction. 14. The process according to claim 12 , characterized in that the light fraction ( 90 ), or part of it, is recirculated to step (d) ( 130 ) as solvent ( 60 ). 15. The process according to claim 1 , characterized in that heating ( 110 ) the mixture ( 30 ) of step (a) is performed at a temperature from 300° C. and 340° C., and/or at a pressure from 90 bar to 140 bar. 16. The process according to claim 1 , characterized in that the heating ( 130 ) the oil phase ( 50 ) of step (c) is performed at a temperature from 370° C. to 410° C. and/or at a pressure from 1 to 100 bar. 17. The process according to claim 1 , characterized in that the heating of step (b) ( 110 ) is performed for 3-60 minutes and/or of step (d) ( 130 ) is performed for 5-30 minutes. 18. The process according to claim 1 , characterized in that heat from one or more product streams is used to heat up feed streams. 19. A renewable product comprising the light fraction ( 90 ) of claim 12 . 20. The process according to claim 1 , characterized in that the amount of lignin feedstock is 5-25 wt % of the total amount of lignin and aqueous solution by weight. 21. The process according to claim 1 , characterized in that said solvent ( 60 ) in step (d) is crude tall oil. 22. The process according to claim 1 , characterized in that the pH of the aqueous phase ( 53 ) is 4 to 8. 23. The process according to claim 1 , characterized in that lignin ( 10 ) is kraft lignin separated from black liquor and the lignin comprises less than 1 wt % of impurities or residues from the black liquor. 24. The process according to claim 1 , characterized in that the lignin ( 10 ) comprises 30-70% organics; 0.1-1% ash; and/or 1.5-70 wt % water. 25. The process according to claim 1 , characterized in that the lignin ( 10 ) comprises 20 to 36 wt % oxygen daf (dry-ash-free). 26. The process according to claim 10 , characterized in that the oil phase ( 50 , 80 ) comprises below 20 wt % oxygen.
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