IP Library › Granted Patent US 10,040,746
Granted Patent B2
US 10,040,746 · App. 15/210,586 · Granted Aug 7, 2018

Carboxylic acid recovery from magnesium carboxylate mixture

Inventors: Adriaan Dirk Kon (Meerkerk, NL); André Banier De Haan (Best, NL); Paulus Loduvicus Johannes Van Der Weide (Breda, NL); Tanja Ðekic {hacek over (Z)}ivkovic (Den Bosch, NL); Lucien Henri Leander Jozef De Koninck (Dongen, NL)
Assignee: PURAC BIOCHEM B.V.
C07C51/02B01J39/05B01J49/53C01B7/035C01F5/02C01F5/10C01F5/16C01F5/30
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Quick Facts
Patent No.
US 10,040,746
App. No.
15/210,586
Granted
Aug 7, 2018
Kind
B2
Abstract

The invention is directed to a method for recovering carboyxlic acid from an magnesium carboxylate containing aqueous mixture, including the steps of: contacting the aqueous mixture with an acidic ion exchanger, thereby forming a carboxylic acid mixture and an ion exchanger loaded with magnesium ions; contacting the ion exchanger loaded with magnesium ions with a hydrochloric acid solution, thereby forming a magnesium chloride solution; and thermally decomposing the magnesium chloride solution at a temperature of at least 300° C., thereby forming magnesium oxide (MgO) and hydrogen chloride (HCl).

Claims (22)

1. A method for recovering carboyxlic acid, comprising the steps of

fermenting a carbohydrate source by means of a microorganism in a fermentation broth to form a carboxylic acid and neutralising at least part of the carboxylic acid by addition of a magnesium base thereby forming a fermentation medium comprising a magnesium carboxylate salt,

subjecting the fermentation medium to a step wherein solid matter is removed to form an aqueous mixture,

contacting the aqueous mixture with an acidic ion exchanger, thereby forming a carboxylic acid mixture and an ion exchanger loaded with magnesium ions; and

contacting the ion exchanger loaded with magnesium ions with a hydrochloric acid solution, thereby forming a magnesium chloride solution; and

thermally decomposing the magnesium chloride solution at a temperature of at least 300° C., thereby forming magnesium oxide (MgO) and hydrogen chloride (HCl).

2. The method according to claim 1 , further comprising

dissolving the HCl in water, thereby obtaining a HCl solution; and

bringing the MgO in contact with water, thereby obtaining Mg(OH) 2 .

3. The method according to claim 2 , wherein the HCl solution is recycled for use in contacting the ion exchanger loaded with magnesium ions.

4. The method according to claim 1 , wherein MgO and/or Mg(OH) 2 is recycled for use in a fermentation process.

5. The method according to claim 1 , wherein at least part of the carboxylic acid mixture is fed back to the aqueous mixture.

6. The method according to claim 1 , wherein the ion exchanger loaded with magnesium ions is washed with water before contacting it with the hydrochloric acid solution.

7. The method according to claim 1 , wherein the acidic ion exchanger is strongly acidic and comprises one or more sulphonic acid and/or phosphonic acid groups.

8. The method according to claim 1 , wherein the acidic ion exchanger is a solid acidic ion exchanger.

9. The method according to claim 1 , wherein the ion exchange step is conducted in an ion exchange column.

10. The method according to claim 1 , wherein the ion exchange step is conducted in a fluidized bed or a simulated moving bed of polymeric ion exchange resin beads.

11. The method according to claim 1 , wherein the acidic ion exchanger is a liquid acidic ion exchanger.

12. The method according to claim 11 , wherein the acidic ion exchanger is an organic compound comprising one or more sulphonic acid and/or phosphonic acid groups, wherein the acidic ion exchanger is optionally dissolved in a hydrophobic solvent.

13. The method according to claim 1 , wherein the carboxylic acid is selected from the group consisting of lactic acid, succinic acid, propionic acid, 3-hydroxypropionic acid, hydroxybutyric acid, citric acid, fumaric acid, itaconic acid, adipic acid, acrylic acid, levulinic acid, maleic acid, terephthalic acid, 2,5-furandicarboxylic acid, lactylic acids and fatty acids.

14. The method according to claim 1 , wherein at least 99 wt. % of the aqueous mixture is in liquid or dissolved form, based on the total weight of the aqueous mixture.

15. The method according to claim 1 , wherein contacting the aqueous mixture with the acidic cation exchanger is conducted at a temperature of at least 40° C.

Priority Claims (1)
EP 12169359 · May 24, 2012 · regional
Continuity (3)
Continuation 14402441
Provisional Application 61651040 · May 24, 2012
Related Publication 20160318837A1 · Nov 3, 2016