IP Library Granted Patent US 7,399,323
Granted Patent B2
US 7,399,323 · App. 11/869,673 · Granted Jul 15, 2008

Fuel compositions comprising farnesane and farnesane derivatives and method of making and using same

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,399,323
App. No.
11/869,673
Granted
Jul 15, 2008
Kind
B2
Abstract

A fuel composition comprises farnesane and/or farnesane derivatives and a conventional fuel component selected from diesel fuel, jet fuel, kerosene or gasoline. The farnesane or farnesane derivative can be used as a fuel component or as a fuel additive in the fuel composition. The fuel composition may further comprise a conventional fuel additive. Methods of making and using the fuel composition are also disclosed.

Claims (34)

1. A fuel composition comprising or obtainable from a mixture comprising:

(a) an isoprenoid compound having the formula:

or a stereoisomer thereof, wherein Z is H, O—R, or O—C(═O)R; and R is H, alkyl, cycloalkyl, aryl, alkaryl, or aralkyl;

(b) a petroleum-based fuel; and

(c) a fuel additive,

wherein the amount of the isoprenoid compound is at least about 5 vol.% and the amount of the petroleum-based fuel is at least about 5 vol. %, both amounts based on the total volume of the fuel composition, and wherein the fuel composition has a flash point equal to or greater than 38° C. and has an initial boiling point between about 100° C. and about 200° C.

2. The fuel composition of claim 1 , wherein the fuel composition has a T90 distillation temperature from about 270° C. to about 350° C.

3. The fuel composition of claim 1 , wherein the amount of the isoprenoid compound is less than about 75 vol. %, based on the total volume of the fuel composition.

4. The fuel composition of claim 1 , wherein the amount of the isoprenoid compound is from about 5 vol. % to about 10 vol. %, based on the total volume of the fuel composition.

5. The fuel composition of claim 1 , wherein the amount of the isoprenoid compound is from about 15 vol. % to about 25 vol. %, based on the total volume of the fuel composition.

6. The fuel composition of claim 1 , wherein the amount of the isoprenoid compound is from about 45 vol. % to about 65 vol %, based on the total volume of the fuel composition.

7. The fuel composition of claim 1 , wherein the petroleum-based fuel is petrodiesel.

8. The fuel composition of claim 1 , wherein the fuel additive is at least one additive selected from the group consisting of an antioxidant, a cetane improver, a stabilizer, a lubricity improver, and combinations thereof.

9. The fuel composition of claim 1 , wherein Z is H.

10. A method of making a fuel composition comprising obtaining a petroleum distillate and adding an isoprenoid compound having the formula

and a fuel additive thereto, wherein Z is H, O—R, or O—C(═O)R; and R is H, alkyl, cycloalkyl, aryl, alkaryl, or aralkyl, wherein the amount of the petroleum distillate is at least about 5 vol. % and the amount of the isoprenoid compound is at least about 5 vol. %, both amounts based on the total volume of the fuel composition, and wherein the fuel composition has a flash point equal to or greater than 38° C. and has an initial boiling point between about 100° C. and about 200° C.

11. The method of claim 10 , wherein the amount of the isoprenoid compound is less than about 65 vol. % based on the total volume of the fuel composition.

12. The method of claim 10 , wherein the fuel composition has a T90 distillation temperature from about 282° C. and about 338° C.

13. The method of claim 12 , wherein the method further comprises chemically converting a C 15 isoprenoid starting material from a biological source to an isoprenoid compound having the formula

wherein Z is H, O—R, or O—C(═O)R; and R is H, alkyl, cycloalkyl, aryl, alkaryl, or aralkyl;

wherein said converting is prior to adding the isoprenoid compound to the petroleum distillate.

14. The method of claim 13 , wherein the C 15 isoprenoid starting material is α-farnesene, β-farnesene or a combination thereof.

15. The method of claim 10 , wherein the fuel additive is at least one additive selected from the group consisting of an antioxidant, a cetane improver, a corrosion inhibitor, a lubricity improver, and combinations thereof.

16. The method of claim 10 , wherein the petroleum distillate is petrodiesel.

17. The method of claim 10 , wherein Z is H.

18. A vehicle comprising an internal combustion engine, a fuel tank connected to the internal combustion engine, and a fuel composition in the fuel tank, wherein the fuel composition comprises:

(a) isoprenoid compound having the formula

or a stereoisomer thereof,

wherein Z is H, O—R, or O—C(═O)R,; and R is H, alkyl, cycloalkyl, aryl, alkaryl or aralkyl;

(b) a petroleum-based fuel; and

(c) a fuel additive,

wherein the amount of the isoprenoid compound is at least about 5 vol. % and the amount of the petroleum-based fuel is at least about 5 vol. %, both amounts based on the total volume of the fuel composition, and wherein the fuel composition has a flash point equal to or greater than 38° C. and has an initial boiling point from about 100° C. to 200° C., and wherein the fuel composition is used to power the internal combustion engine.

19. The vehicle of claim 18 , wherein the internal combustion engine is a diesel engine.

20. The vehicle of claim 18 , wherein Z is H.

Assignments (14)
SECURITY INTEREST Recorded May 24, 2024
From: AMYRIS, INC.
To: EUAGORE, LLC
Reel/Frame 067528/0467 →
SECURITY INTEREST Recorded Aug 17, 2023
From: AMYRIS, INC.; AMYRIS CLEAN BEAUTY, INC.; AMYRIS FUELS, LLC; AB TECHNOLOGIES LLC; APRINNOVA, LLC; AMYRIS-OLINKA, LLC; ONDA BEAUTY INC.; UPLAND 1 LLC; AMYRIS ECO-FAB LLC; CLEAN BEAUTY 4U HOLDINGS, LLC; AMYRIS CLEAN BEAUTY LATAM LTDA; INTERFACES INDUSTRIA E COMERCIA DE COSMETICOS LTDA; AMYRIS BIOTECHNOLOGIA DO BRASIL LTDA; AMYRIS EUROPE TRADING B.V. (NETHERLANDS); AMYRIS BIO PRODCUTS PORTUGAL, UNIPESSOAL, LDA; BEAUTY LABS INTERNATIONAL LIMITED; AMYRIS UK TRADING LIMITED
To: EUAGORE, LLC
Reel/Frame 064619/0778 →
SECURITY INTEREST Recorded Aug 3, 2023
From: AMYRIS CLEAN BEAUTY, INC.; AMYRIS FUELS, LLC; AB TECHNOLOGIES LLC; AMYRIS, INC.
To: MUIRISC, LLC
Reel/Frame 064492/0518 →
RELEASE OF SECURITY INTEREST Recorded Feb 14, 2023
From: NAXYRIS S.A.
To: AMYRIS, INC.
Reel/Frame 062760/0753 →
RELEASE OF SECURITY INTEREST Recorded Feb 14, 2023
From: SCHOTTENFELD OPPORTUNITIES FUND II, L.P.
To: AMYRIS, INC.
Reel/Frame 062760/0818 →
SECURITY INTEREST Recorded Oct 18, 2022
From: AMYRIS, INC.
To: FORIS VENTURES, LLC
Reel/Frame 061703/0499 →
GRANT OF PATENT SECURITY INTEREST Recorded Nov 20, 2019
From: AMYRIS, INC.
To: SCHOTTENFELD OPPORTUNITIES FUND II, L.P.
Reel/Frame 051072/0310 →
SECURITY INTEREST Recorded Aug 16, 2019
From: AMYRIS, INC.
To: NAXYRIS S.A.
Reel/Frame 050081/0106 →
CHANGE OF NAME Recorded Nov 17, 2017
From: AMYRIS BIOTECHNOLOGIES
To: AMYRIS, INC.
Reel/Frame 044483/0245 →
RELEASE OF SECURITY INTEREST Recorded Mar 28, 2014
From: TOTAL ENERGIES NOUVELLES ACTIVITES USA, SAS (F/K/A TOTAL GAS & POWER USA, SAS)
To: AMYRIS, INC.
Reel/Frame 032554/0001 →
RELEASE OF SECURITY INTEREST Recorded Mar 27, 2014
From: TOTAL ENERGIES NOUVELLES ACTIVITIES USA, SAS (F/K/A TOTAL GAS & POWER USA, SAS)
To: AMYRIS, INC.
Reel/Frame 032551/0828 →
SECURITY AGREEMENT Recorded Nov 8, 2013
From: AMYRIS, INC.
To: TOTAL ENERGIES NOUVELLES ACTIVITES USA
Reel/Frame 031607/0314 →
SECURITY AGREEMENT Recorded May 8, 2013
From: AMYRIS, INC.
To: TOTAL GAS & POWER USA, SAS
Reel/Frame 030378/0447 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 11, 2008
From: RENNINGER, NEIL STEPHEN; MCPHEE, DEREK JAMES
To: AMYRIS BIOTECHNOLOGIES, INC.
Reel/Frame 021079/0936 →