IP Library Granted Patent US 9,909,077
Granted Patent B2
US 9,909,077 · App. 15/024,707 · Granted Mar 6, 2018

Production of products from feedstocks containing free fatty acids

Inventors: David A. Slade (Ames, IA); Derek J. Winkel (Ankeny, IA); Jared A. Downey (Ames, IA)
Assignee: REG Seneca, LLC
C10L1/026C07C67/02C07C67/08C07C69/24C11C3/02C10L2200/0476C10L2270/026Y02E50/13
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Quick Facts
Patent No.
US 9,909,077
App. No.
15/024,707
Granted
Mar 6, 2018
Kind
B2
Abstract

The present invention provides a method for producing a refined fatty acid alkyl ester (FAAE) product from feed-stocks containing free fatty acids. The method comprises glycerolysis and transesterification processes combined with end-product refining. Products produced from a transesterification reaction are separated into a crude FAAE stream and a crude glycerin stream. The crude glycerin stream is further processed to produce a glyceride stream from which additional FAAEs may be produced.

Claims (35)

1. A method for producing products from a feedstock containing free fatty acids comprising:

a. reacting said feedstock with glycerin in a reactor to produce a first glyceride stream;

b. reacting said first glyceride stream with alcohol to produce a reaction mixture;

c. separating said reaction mixture to produce a crude fatty acid alkyl ester stream and a crude glycerin stream;

d. wherein said crude fatty acid alkyl ester stream is a first light phase;

e. separating the crude glycerin stream into a secondary light phase and a second crude glycerin stream, wherein the secondary light phase includes free fatty acids and alkyl esters;

f. converting free fatty acids and alkyl esters in the secondary light phase into glycerides, water, and alcohol and removing water and alcohol to produce a second glyceride stream; and

g. introducing the second glyceride stream into step (a).

2. The method of claim 1 , wherein said secondary light phase comprises free fatty acids, glycerides, alkyl esters, and glycerin.

3. The method of claim 1 , wherein step (e) further comprises separating the secondary light phase into a first secondary light phase and a second secondary light phase.

4. The method of claim 3 , wherein said first secondary light phase comprises alkyl esters, free fatty acids, and glycerides.

5. The method of claim 3 , wherein said second secondary light phase comprises glycerin.

6. The method of claim 3 , further comprising the step of combining said second secondary light phase with said second crude glycerin stream.

7. A method for producing products from a feedstock containing free fatty acids comprising:

a. reacting said feedstock with glycerin in a first glycerolysis process to produce a first glyceride stream;

b. reacting said first glyceride stream with alcohol in a transesterification process to produce a reaction mixture;

c. separating said reaction mixture to produce a crude fatty acid alkyl ester stream and a crude glycerin stream, wherein said crude fatty acid alkyl ester stream is a first light phase;

d. separating said crude glycerin stream into a secondary light phase and a second crude glycerin stream;

e. separating said secondary light phase into a first secondary light phase and a second secondary light phase; and

f. introducing said first secondary light phase to glycerin to produce a second glyceride stream.

8. The method of claim 7 , further comprising the step of combining said second secondary light phase with said second crude glycerin stream.

9. A method for producing glycerides from alkyl esters and free fatty acids separated from a crude glycerin stream which has been produced by a first transesterification process and separated from a first light phase, said method comprising:

a. separating said crude glycerin stream into a heavy phase and a secondary light phase, wherein the secondary light phase includes alkyl esters and free fatty acids;

b. reacting said alkyl esters and free fatty acids in the secondary light phase with glycerin to produce a reaction mixture containing glycerides, water, and alcohol;

c. removing water and alcohol from said reaction mixture to produce a glyceride stream.

10. The method of claim 9 , further comprising the step of introducing said glyceride stream into at least one of the first transesterification process and a second transesterification process.

11. The method of claim 9 , further comprising the step of introducing said glyceride stream into a glycerolysis process.

12. The method of claim 9 , further comprising the step of separating said secondary light phase into a first secondary light phase and a second secondary light phase prior to the reacting step of claim 9 (b), wherein the reacting step of claim 9 (b) uses reactants from said first secondary light phase to produce said glyceride stream.

13. The method of claim 7 further comprising the step of introducing the second glyceride stream into one of step (a) and step (b) to produce additional fatty acid alkyl esters.

14. The method of claim 7 , wherein said first secondary light phase comprises alkyl esters, free fatty acids, and glycerides.

15. The method of claim 7 , wherein said second secondary light phase comprises glycerin.

16. The method of claim 12 , wherein said first secondary light phase comprises alkyl esters, free fatty acids, and glycerides.

17. The method of claim 12 , wherein said second secondary light phase comprises glycerin.

18. The method of claim 1 , further comprising treating the crude glycerin stream with acid to produce a neutralized crude glycerin stream.

19. The method of claim 7 , further comprising treating the crude glycerin stream with acid to produce a neutralized crude glycerin stream.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Jul 1, 2022
From: UMB BANK, N.A., AS COLLATERAL TRUSTEE
To: REG SYNTHETIC FUELS, LLC; RENEWABLE ENERGY GROUP, INC.; REG SENECA, LLC; REG BIOFUELS, LLC
Reel/Frame 060562/0428 →
PATENT SECURITY AGREEMENT Recorded Jun 19, 2021
From: REG SENECA, LLC
To: UMB BANK, N.A., AS COLLATERAL TRUSTEE
Reel/Frame 056628/0607 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 5, 2021
From: SLADE, DAVID A.; WINKEL, DEREK J.; DOWNEY, JARED A.
To: REG SENECA, LLC
Reel/Frame 056140/0542 →
Continuity (2)
Provisional Application 61844201 · Jul 9, 2013
Related Publication 20160289578A1 · Oct 6, 2016