IP Library Granted Patent US 9,464,045
Granted Patent B2
US 9,464,045 · App. 14/850,207 · Granted Oct 11, 2016

Process for the preparation of methionine

Inventors: Martin Koerfer (Kahl, DE); Hans Joachim Hasselbach (Gelnhausen, DE); Stefan Reichert (Frankfurt, DE); Harald Jakob (Hasselroth, DE); Christoph Weckbecker (Gruendau, DE); Klaus Huthmacher (Gelnhausen, DE); Horst Krull (Hanau, DE); Bernd Drapal (Alzenau, DE); Rainer Peter (Krombach, DE)
Assignee: EVONIK DEGUSSA GmbH
C07C319/28C07C319/12C07C319/20C07C319/26C07C323/52Y02P20/142
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Quick Facts
Patent No.
US 9,464,045
App. No.
14/850,207
Granted
Oct 11, 2016
Kind
B2
Abstract

This disclosure relates to a process for preparing D,L-methionine by feeding carbon dioxide to an aqueous potassium methioninate solution obtained by hydrolysis of 5-(2-methylmercaptoethyl)hydantoin, in order to precipitate out crude methionine, which is separated off and purified. In this process an aqueous solution of the separated-off crude methionine is purified by recrystallization from a solution containing potassium ions and also a crystallization additive. The crystallization additive is a nonionic or anionic surfactant, or a mixture of different nonionic or anionic surfactants. The recrystallization occurs by introducing a 60 to 110° C.-hot methionine solution into a 35 to 80° C.-warm methionine suspension, a temperature of which is lower than that of the introduced solution, such that the temperature of the methionine suspension being maintained between 35 and 80° C. during the addition. The crystallization additive is a sorbitan fatty acid ester or a mixture of different sorbitan fatty acid esters.

Claims (18)

1. A process for preparing D,L-methionine, the process comprising:

feeding carbon dioxide to an aqueous potassium methioninate solution obtained by hydrolysis of 5-(2-methylmercaptoethyl)hydantoin, thereby precipitating out crude methionine, and

purifying an aqueous solution of a separated-off crude methionine

by recrystallization from a solution comprising potassium ions and a crystallization additive;

wherein the recrystallization takes place by introducing a 60 to 110° C-hot methionine solution into a 35 to 80° C-warm methionine suspension, wherein a temperature of the warm methionine suspension is lower than a temperature of the introduced hot methionine solution, wherein a temperature of a mixture formed of the hot methionine solution and the warm methionine suspension is maintained between 35 and 80° C. during the introduction; and

wherein the crystallization additive is a polyethoxylated sorbitan stearate.

2. The process of claim 1 , wherein the polyethoxylated sorbitan stearate is a polyethoxylated sorbitan tristearate of the formula:

wherein w+x+y+z=20.

3. The process of claim 1 , wherein a concentration of the crystallization additive in the solution from which the recrystallization takes place is at least 50 ppm based on the total mass of the solution and/or suspension.

4. The process of claim 1 , wherein the solution from which the recrystallization takes place additionally comprises an antifoam.

5. The process of claim 4 , wherein the antifoam comprises silicone oil.

6. The process of claim 1 , wherein a potassium ion concentration in the solution from which the recrystallization takes places is from 1 to 30 g/kg.

7. The process of claim 1 , wherein a potassium ion concentration in the solution from which the recrystallization takes place is 5 to 10 g/kg.

8. The process of claim 1 , wherein the recrystallization takes place by introducing an 85 to 110° C-hot crude methionine solution into a 35 to 60° C.-warm methionine suspension, wherein a temperature of the mixture is kept constant between 35 and 60° C.

9. The process of claim 1 , wherein the recrystallization is carried out in two stages, wherein in the first recrystallization stage, an 85 to 110° C.-hot crude methionine solution is introduced into a 60 to 80° C-warm methionine suspension, thereby forming a first mixture, wherein a temperature of the first mixture is kept constant between 60 and 80° C. and wherein a 60 to 80° C-warm methionine suspension obtained in the first recrystallization stage is introduced into a 35 to 60° C-warm methionine suspension in the second recrystallization stage, wherein a temperature of a mixture obtained in the second recrystallization stage is kept constant between 35 and 60° C.

10. The process of claim 1 , wherein the recrystallization takes place by vacuum crystallization, wherein the recrystallization is carried out in two stages, and wherein a pressure in the first recrystallization stage is from 100 to 1000 mbar and from 35 to 200 mbar in the second recrystallization stage.

11. The process of claim 10 , wherein in addition to the first and second recrystallization stages, the process comprises further recrystallization stages, and a part of the methionine suspension is removed from the first and/or at least one of the other recrystallization stages and is returned via a circulation circuit, wherein a temperature of a methionine suspension in the circulation circuit is increased by 6 to 12° C.

12. The process of claim 1 , wherein the process comprises further recrystallization stages, and a part of the methionine suspension is removed from a first and/or at least one of the other recrystallization stages and is returned via a circulation circuit, wherein a temperature of a methionine suspension in the circulation circuit is increased by 6 to 12° C.

Assignments (1)
CHANGE OF NAME Recorded Sep 3, 2021
From: EVONIK DEGUSSA GMBH
To: EVONIK OPERATIONS GMBH
Reel/Frame 057405/0513 →
Priority Claims (1)
EP 12160257 · Mar 20, 2012 · regional
Continuity (2)
Continuation 14386165
Related Publication 20160068480A1 · Mar 10, 2016