Method for improving biodiesel fuel
View Patent ↗The addition of strong neutralizing amines to react with free fatty acid in biodiesel fuels that may be left from some synthesis routes can lower the total acid number (TAN) of the biodiesel fuel. Surprisingly, the strong neutralizing amines do not interfere with the biodiesel fuel itself which may be primarily fatty acid methyl esters. These strong neutralizing amines may also improve the oxidative stability of biodiesel fuels.
1. A method for improving a biodiesel fuel comprising fatty acid methyl esters and free fatty acids, the method comprising adding to the biodiesel fuel an additive selected from the group consisting of a quaternary ammonium hydroxide, a quaternary ammonium alkoxide, and mixtures thereof, where the quaternary ammonium hydroxide has the formula selected from the group consisting of R 1 R 2 R 3 N + OH OH − , R 1 R 2 R 3 N + CH 2 CHR 5 OH OH − and R 1 R 2 R 3 R 4 N + OH − and the quaternary ammonium alkoxide has the formula R 1 R 2 R 3 R 4 N + O − , and mixtures thereof, where:
R 1 and R 2 are independently selected from the group consisting of alkyl groups of from 1 to about 18 carbon atoms, aryl groups of from 8 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms,
R 3 is selected from the group consisting of alkyl groups of from 2 to about 18 carbon atoms, aryl groups of from 6 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms, provided, however, that R 2 and R 3 may be joined to form a heterocyclic ring including the N and optionally an oxygen atom,
R 4 is selected from the group consisting of hydrogen, alkyl groups of from 2 to about 18 carbon atoms, alkylaryl groups of from 7 to about 18 carbon atoms, —(CH 2 CH 2 O) n H, where n is from 1 to about 18,
where m and p are independently selected from integers from 0 to about 18, except that the sum m+p is less than or equal to about 18, and
—CHR 5 CHR 6 Y, where R 5 and R 6 are independently selected from the group consisting of hydrogen, alkyl groups of from 1 to about 18 carbon atoms, aryl groups of from 6 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms, and Y is a non-acidic group selected from the group consisting of —OH, —SR 7 and —NR 7 R 8 , where R 7 and R 8 are independently selected from the group consisting of hydrogen, alkyl groups of from 1 to about 18 carbon atoms, aryl groups of from 6 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms, and
R 5 is selected from the group consisting of hydrogen, alkyl groups of from 1 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms.
2. The method of claim 1 where the additive is added to the biodiesel fuel at least equivalent to 0.01 mg KOH/g of the biodiesel fuel.
3. The method of claim 1 where the additive is added to the biodiesel fuel in an amount from about 20 to about 10,000 ppm.
4. The method of claim 1 where R 4 is —(CH 2 CH 2 O) n H where n is as defined therein.
5. The method of claim 1 where the biodiesel fuel is improved by a characteristic selected from the group consisting of:
reduced acid potential as measured by total acid number (TAN);
increased oxidative stability; and both,
as compared with a biodiesel fuel absent the additive.
6. The method of claim 5 where the biodiesel fuel has reduced acid potential as measured by TAN of between about 0.01 and about 0.9 mg KOH/g of biodiesel fuel.
7. A method for improving a biodiesel fuel comprising fatty acid methyl esters and free fatty acids with a minimum ester content of 96.5 wt %, the method comprising adding to the biodiesel fuel from about 20 to about 10,000 ppm of an additive, based on the biodiesel fuel, where the additive is selected from the group consisting of a quaternary ammonium hydroxide, a quaternary ammonium alkoxide, and mixtures thereof, where the quaternary ammonium hydroxide has the formula selected from the group consisting of R 1 R 2 R 3 N + OH OH − , R 1 R 2 R 3 N + CH 2 CHR 5 OH OH − and R 1 R 2 R 3 R 4 N + OH − and the quaternary ammonium alkoxide has the formula R 1 R 2 R 3 R 4 N + O − , and mixtures thereof, where:
R 1 and R 2 are independently selected from the group consisting of alkyl groups of from 1 to about 18 carbon atoms, aryl groups of from 8 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms,
R 3 is selected from the group consisting of alkyl groups of from 2 to about 18 carbon atoms, aryl groups of from 6 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms, provided, however, that R 2 and R 3 may be joined to form a heterocyclic ring including the N and optionally an oxygen atom,
R 4 is selected from the group consisting of hydrogen, alkyl groups of from 2 to about 18 carbon atoms, alkylaryl groups of from 7 to about 18 carbon atoms, —(CH 2 CH 2 O) n H, where n is from 1 to about 18,
where m and p are independently selected from integers from 0 to about 18, except that the sum m+p is less than or equal to about 18, and —CHR 5 CHR 6 Y, where R 5 and R 6 are independently selected from the group consisting of hydrogen, alkyl groups of from 1 to about 18 carbon atoms, aryl groups of from 6 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms, and Y is a non-acidic group selected from the group consisting of —OH, —SR 7 and —NR 7 R 8 , where R 7 and R 8 are independently selected from the group consisting of hydrogen, alkyl groups of from 1 to about 18 carbon atoms, aryl groups of from 6 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms, and
R 5 is selected from the group consisting of hydrogen, alkyl groups of from 1 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms,
where the biodiesel fuel is improved by a characteristic selected from the group consisting of: reduced acid potential as measured by total acid number (TAN) of; increased oxidative stability; and both, as compared with a biodiesel fuel absent the additive.
8. The method of claim 7 where the additive is added to the biodiesel fuel at least equivalent to 0.01 mg KOH/g of the biodiesel fuel.
9. The method of claim 7 where R 4 is —(CH 2 CH 2 O) n H where n is as defined therein.
10. The method of claim 7 where the biodiesel fuel has reduced acid potential as measured by TAN of between about 0.01 and about 0.9 mg KOH/g of biodiesel fuel.
11. An improved biodiesel fuel comprising:
fatty acid methyl esters;
free fatty acids;
an additive selected from the group consisting of a quaternary ammonium hydroxide, a quaternary ammonium alkoxide, and mixtures thereof, where the quaternary ammonium hydroxide has the formula selected from the group consisting of R 1 R 2 R 3 N + OH OH − , R 1 R 2 R 3 N + CH 2 CHR 5 OH OH − and R 1 R 2 R 3 R 4 N + OH − and the quaternary ammonium alkoxide has the formula R 1 R 2 R 3 R 4 N + O − , and mixtures thereof, where:
R 1 and R 2 are independently selected from the group consisting of alkyl groups of from 1 to about 18 carbon atoms, aryl groups of from 8 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms,
R 3 is selected from the group consisting of alkyl groups of from 2 to about 18 carbon atoms, aryl groups of from 6 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms, provided, however, that R 2 and R 3 may be joined to form a heterocyclic ring including the N and optionally an oxygen atom,
R 4 is selected from the group consisting of hydrogen, alkyl groups of from 2 to about 18 carbon atoms, alkylaryl groups of from 7 to about 18 carbon atoms, —(CH 2 CH 2 O) n H, where n is from 1 to about 18
where m and p are independently selected from integers from 0 to about 18, except that the sum m+p is less than or equal to about 18, and —CHR 5 CHR 6 Y, where R 5 and R 6 are independently selected from the group consisting of hydrogen, alkyl groups of from 1 to about 18 carbon atoms, aryl groups of from 6 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms, and Y is a non-acidic group selected from the group consisting of —OH, —SR 7 and —NR 7 R 8 , where R 7 and R 8 are independently selected from the group consisting of hydrogen, alkyl groups of from 1 to about 18 carbon atoms, aryl groups of from 6 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms, and
R 5 is selected from the group consisting of hydrogen, alkyl groups of from 1 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms,
where at least some of the additive has reacted with the H 2 S and/or mercaptan.
12. The improved biodiesel fuel of claim 11 where the additive present is at least equivalent to 0.01 mg KOH/g of the biodiesel fuel.
13. The improved biodiesel fuel of claim 11 where the additive is present in an amount from about 20 to about 10,000 ppm.
14. The improved biodiesel fuel of claim 11 where R 4 is —(CH 2 CH 2 O) n H where n is as defined therein.
15. The improved biodiesel fuel of claim 11 where the biodiesel fuel is improved by a characteristic selected from the group consisting of:
reduced acid potential as measured by total acid number (TAN);
increased oxidative stability of the biodiesel fuel; and both,
as compared with a biodiesel fuel absent the additive.
16. The improved biodiesel fuel of claim 15 where the biodiesel fuel has reduced acid potential as measured by TAN of between about 0.01 and about 0.9 mg KOH/g of biodiesel fuel.
17. An improved biodiesel fuel comprising:
fatty acid methyl esters, where the biodiesel fuel has a minimum ester content of 96.5 wt %;
free fatty acids;
about 20 to about 10,000 ppm of an additive, based on the biodiesel fuel, where the additive is selected from the group consisting of a quaternary ammonium hydroxide, a quaternary ammonium alkoxide, and mixtures thereof, where the quaternary ammonium hydroxide has the formula selected from the group consisting of R 1 R 2 R 3 N + OH OH − , R 1 R 2 R 3 N + CH 2 CHR 5 OH OH − and R 1 R 2 R 3 R 4 N + OH − and the quaternary ammonium alkoxide has the formula R 1 R 2 R 3 R 4 N + O − , and mixtures thereof, where:
R 1 and R 2 are independently selected from the group consisting of alkyl groups of from 1 to about 18 carbon atoms, aryl groups of from 8 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms,
R 3 is selected from the group consisting of alkyl groups of from 2 to about 18 carbon atoms, aryl groups of from 6 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms, provided, however, that R 2 and R 3 may be joined to form a heterocyclic ring including the N and optionally an oxygen atom,
R 4 is selected from the group consisting of hydrogen, alkyl groups of from 2 to about 18 carbon atoms, alkylaryl groups of from 7 to about 18 carbon atoms, —(CH 2 CH 2 O) n H, where n is from 1 to about 18
where m and p are independently selected from integers from 0 to about 18, except that the sum m+p is less than or equal to about 18, and —CHR 5 CHR 6 Y, where R 5 and R 6 are independently selected from the group consisting of hydrogen, alkyl groups of from 1 to about 18 carbon atoms, aryl groups of from 6 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms, and Y is a non-acidic group selected from the group consisting of —OH, —SR 7 and —NR 7 R 8 , where R 7 and R 8 are independently selected from the group consisting of hydrogen, alkyl groups of from 1 to about 18 carbon atoms, aryl groups of from 6 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms, and
R 5 is selected from the group consisting of hydrogen, alkyl groups of from 1 to about 18 carbon atoms and alkylaryl groups of from 7 to about 18 carbon atoms,
where at least some of the additive has reacted with the H 2 S and/or mercaptan, where the biodiesel fuel is improved by a characteristic selected from the group consisting of: reduced acid potential as measured by total acid number (TAN); increased oxidative stability of the biodiesel fuel; and both, as compared with a biodiesel fuel absent the additive.
18. The improved biodiesel fuel of claim 17 where the additive is present at least equivalent to 0.01 mg KOH/g of the biodiesel fuel.
19. The improved biodiesel fuel of claim 17 where R 4 is —(CH 2 CH 2 O) n H where n is as defined therein.
20. The improved biodiesel fuel of claim 17 where the biodiesel fuel has reduced acid potential as measured by TAN of between about 0.01 and about 0.9 mg KOH/g of biodiesel fuel.