IP Library Granted Patent US 9,428,816
Granted Patent B2
US 9,428,816 · App. 13/715,311 · Granted Aug 30, 2016

Method of treating ethanol production byproducts

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Quick Facts
Patent No.
US 9,428,816
App. No.
13/715,311
Granted
Aug 30, 2016
Kind
B2
Abstract

A method of treating ethanol production byproduct is provided by treating wet distillers grain or stillage with a solution containing at least one α-hydroxysulfonic acid to produce at least one fermentable sugar containing product. Fermentable sugar useful for the production of biofuels or ethanol can be produced from such methods. The α-hydroxysulfonic acid can be easily removed from the product and recycled.

Claims (27)

1. A method of treating ethanol production byproduct comprising: (a) providing a wet distillers grain containing moisture; (b) contacting the wet distillers grain with a solution comprising at least one α-hydroxysulfonic acid thereby hydrolyzing the wet distillers grain to produce at least one fermentable sugar containing product; and (c) removing at least a portion of said α-hydroxysulfonic acid in its component form from said fermentable sugar containing product by a process consisting of heating and/or reducing pressure to produce an acid-removed product containing at least one fermentable sugar.

2. The method of claim 1 , further comprising recycling the removed α-hydroxysulfonic acid obtained in step (c) to step (b) as components or in its recombined form.

3. The method of claim 1 , further comprising fermenting said acid-removed product to produce at least one alcohol.

4. The method of claim 1 , further comprising hydrolyzing said acid-removed product to produce a hydrolyzed product.

5. The method of claim 4 , further comprising fermenting said hydrolyzed product to produce at least one alcohol.

6. The method of claim 1 , wherein said α-hydroxysulfonic acid is present in an amount of 1% wt. to 55% wt., based on the solution.

7. The method of claim 1 , wherein said α-hydroxysulfonic acid is produced from a carbonyl compound or a precursor to a carbonyl compound combined with sulfur dioxide and water.

8. The method of claim 1 , wherein said α-hydroxysulfonic acid is in-situ generated.

9. The method of claim 1 , wherein step (b) is carried out at a temperature within the range of 50° C. to 150° C. and a pressure within the range of 1 barg to 10 barg.

10. A method comprising: (a) providing grain; (b) grinding said grain to produce ground grain; (c) treating said ground grain to produce a fermentable sugar mixture; (d) fermenting the fermentable sugar mixture to produce a fermented product containing ethanol, solids and water; (e) separating said fermented product to produce ethanol and stillage containing water; (f) contacting at least a portion of said stillage containing water with a solution comprising at least one α-hydroxysulfonic acid thereby hydrolyzing said stillage to produce at least one fermentable sugar containing product; and (g) removing at least a portion of said α-hydroxysulfonic acid in its component form from said fermentable sugar containing product by a process consisting of heating and/or reducing pressure to produce an acid-removed product containing at least one fermentable sugar.

11. The method of claim 10 , further comprising recycling the removed α-hydroxysulfonic acid obtained in step (g) to step (f) as components or in its recombined form.

12. The method of claim 10 , further comprising fermenting said acid-removed product to produce at least one alcohol.

13. The method of claim 10 , further comprising hydrolyzing said acid-removed product to produce a hydrolyzed product.

14. The method of claim 13 , further comprising fermenting said hydrolyzed product to produce at least one alcohol.

15. The method of claim 10 , wherein said α-hydroxysulfonic acid is present in an amount of 1% wt. to 55% wt., based on the solution.

16. The method of claim 10 , wherein said α-hydroxysulfonic acid is produced from a carbonyl compound or a precursor to a carbonyl compound combined with sulfur dioxide and water.

17. The method of claim 10 , wherein said α-hydroxysulfonic acid is in-situ generated.

18. The method of claim 10 , wherein step (f) is carried out at a temperature within the range of 50° C. to 150° C. and a pressure within the range of 1 barg to 10 barg.

19. A method comprising: (a) providing grain; (b) grinding said grain to produce ground grain; (c) treating said ground grain to produce fermentable sugar mixture; (d) fermenting said fermentable sugar mixture to produce a fermented product containing ethanol, solids and water; (e) separating said fermented product to produce ethanol and stillage; (f) separating said stillage to produce thin stillage and wet distillers grain containing moisture; and (g) contacting at least a portion of said wet distillers grain containing moisture with a solution comprising at least one α-hydroxysulfonic acid thereby hydrolyzing said wet distillers grain to produce at least one fermentable sugar containing product; and (h) removing at least a portion of said α-hydroxysulfonic acid in its component form from said fermentable sugar containing product by a process consisting of heating and/or reducing pressure to produce an acid-removed product containing at least one fermentable sugar.

20. The method of claim 19 , further comprising recycling the removed α-hydroxysulfonic acid obtained in step (h) to step (g) as components or in its recombined form.

21. The method of claim 19 , further comprising fermenting said acid-removed product to produce at least one alcohol.

22. The method of claim 19 , further comprising hydrolyzing said acid-removed product to produce a hydrolyzed product.

23. The method of claim 22 , further comprising fermenting said hydrolyzed product to produce at least one alcohol.

24. The method of claim 19 , wherein said α-hydroxysulfonic acid is present in an amount of 1% wt. to 55% wt., based on the solution.

25. The method of claim 19 , wherein said α-hydroxysulfonic acid is produced from a carbonyl compound or a precursor to a carbonyl compound combined with sulfur dioxide and water.

26. The method of claim 19 , wherein said α-hydroxysulfonic acid is in-situ generated.

27. The method of claim 19 , wherein step (g) is carried out at a temperature within the range of 50° C. to about 150° C. and a pressure within the range of 1 barg to 10 barg.

Assignments (2)
CHANGE OF NAME Recorded Mar 7, 2022
From: SHELL OIL COMPANY
To: SHELL USA, INC.
Reel/Frame 059694/0819 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 8, 2013
From: BLACKBOURN, ROBERT LAWRENCE; TETARENKO, PAMELA KAREN; WEIDER, PAUL RICHARD
To: SHELL OIL COMPANY
Reel/Frame 029778/0882 →