Method for Obtaining Biodiesel, Alternative Fuels and Renewable Fuels Tax Credits and Treatment

• US 20090076913A1
• Filed: 07/16/2008
• Published: 03/19/2009
• Est. Priority Date: 09/19/2007
• Status: Abandoned Application

• Current Assignee: Endicott Biofuels II, LLC (Endicott Biofuels, LLC)
• Original Assignee: Endicott Biofuels II, LLC (Endicott Biofuels, LLC)
• Inventors: Morgan, William Douglas
• Application Number:
  US12/174,392
• Publication Number:
  US 20090076913A1
• Time in Patent Office: Days
• US Class Current: 705/14.340
• CPC Class Codes: B01D 3/009 in combination with chemical reactions
• CPC Class Codes: C07C 67/08 by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
• CPC Class Codes: C07C 69/24 esterified with monohydroxylic compounds
• CPC Class Codes: C07C 69/52 Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
• CPC Class Codes: C10G 2300/1011 Biomass
• CPC Class Codes: C10L 1/026 for compression ignition
• CPC Class Codes: C11C 3/003 by esterification of fatty acids with alcohols C11C3/02 takes precedence
• CPC Class Codes: G06Q 30/0234 Rebates after completed purchase
• CPC Class Codes: Y02E 50/10 Biofuels, e.g. bio-diesel
• CPC Class Codes: Y02P 20/10 Process efficiency
• CPC Class Codes: Y02P 30/20 using bio-feedstock

Abstract

The present invention relates to a method of obtaining U.S. Federal and State tax credits, U.S. Federal renewable fuel treatment, and other incentives by production of esters manufactured by the esterification of carboxylic acids using slurry phase, heterogeneous catalyzed, reactive distillation, and sale thereof for U.S. consumption as a renewable fuel.

Claims

1. A method for obtaining U.S. Federal tax credits under Title 26 Sections 40A and/or 6426 for ester based fuels, and/or a method for obtaining Renewable Identification Numbers under the EPA Clean Air Act as amended by the Energy Independence and Security Act of 2007, comprising:

(A) passing one or more carboxylic acid components and an alcohol component countercurrently through an esterification zone maintained under esterification conditions and containing a solid esterification catalyst selected from particulate ion exchange resins having sulphonic acid groups, carboxylic acid groups or both, wherein

(i) the esterification zone comprises a column reactor provided with a plurality of esterification trays mounted one above another, each adapted to hold a predetermined liquid volume and a charge of particles of a solid esterification catalyst thereon, liquid downcomer means associated with each esterification tray adapted to allow liquid phase to pass down the column reactor from each esterification tray but to retain the particles of solid esterification catalyst thereon, and vapor upcomer means associated with each esterification tray adapted to allow vapor to enter each esterification tray from below and to agitate and maintain the suspension of the mixture of liquid and solid esterification catalyst on that esterification tray, each esterification tray having a floor that slopes towards a zone of turbulence under said vapor upcomer means to prevent formation of stagnant zones of particles of catalyst thereon; and

(ii) the less volatile component of the carboxylic acid component and of the alcohol component is supplied in liquid phase to an upper part of the column reactor above the uppermost esterification tray, while the more volatile component of the carboxylic acid component and of the alcohol component is supplied in vapor form beneath the lowermost one of said plurality of esterification trays; and

(iii) vapor comprising said more volatile component and water of esterification is recovered from an upper part of the column reactor; and

(iv) wherein said carboxylic acid ester is recovered from a lower part of the column reactor;

(B) selling or using as fuel the carboxylic acid ester of step (A)(iv) with or without blending said carboxylic acid ester with taxable fuel;

and

(C) having a tax payer use the product of step (B) as a basis for a claim for U.S. Federal tax credits under Title 26 Sections 40A and/or 6426, and/or for U.S. Federal Renewable Identification Numbers under Environmental Protection Agency Clean Air Act as amended by the Energy Independence and Security Act of 2007.

2. A method according to claim 1, wherein the more volatile component is the alcohol component and the less volatile component is the one or more carboxylic acid components.

3. A method according to claim 1, wherein the alcohol component is an alkanol containing from 1 to about 10 carbon atoms.

4. A method according to claim 3, wherein the alkanol is methanol.

5. A method according to claim 3, wherein the water content of the alkanol vapor supplied to the column reactor is less than about 5 mole %.

6. A method according to claim 1, wherein the carboxylic acid component is an aliphatic monocarboxylic acid or a mixture thereof.

7. A method according to claim 6, wherein the carboxylic acid component is a mixture of fatty acids.

8. A method according to claim 1, wherein the carboxylic acid component contains a mixture of rosin acids.

9. A method according to claim 1, wherein the column reactor is operated at a temperature of from about 80°

C. to about 140°

C. and at a pressure of from about 1 bar to about 25 bar.

10. A method according to claim 1, wherein the carboxylic acid ester recovered from a lower part of the column reactor is admixed with additional alcohol component and is passed through a fixed bed of a solid esterification catalyst.

11. The method of claim 1, wherein the carboxylic acids are derived from hydrolysis of mono-, di-, or tri-glycerides.

12. The method of claim 1, wherein the carboxylic acids are distilled from a mixture of fatty acids and glycerides.

13. The method of claim 1, wherein the carboxylic acids are produced by the acidulation of soy, palm, canola, rapeseed, jahtropa, or vegetable oil soapstock.

14. The method of claim 1, wherein the carboxylic acids are produced by the acidulation and fractionation of tall oil soaps.

15. The method of claim 1, wherein the carboxylic acids are derived from hydrolysis and distillation of mixtures of fatty acids and triglycerides.