IP Library Granted Patent US 8,956,520
Granted Patent B2
US 8,956,520 · App. 13/322,702 · Granted Feb 17, 2015

Electrochemical process to prepare chemicals using a cyanide salt

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Quick Facts
Patent No.
US 8,956,520
App. No.
13/322,702
Granted
Feb 17, 2015
Kind
B2
Abstract

The present invention relates to a process comprising the reaction of a cyanide with a hydrogen cyanide-reactive compound, characterized in that the cyanide is a cyanide salt and the process is an electrochemical process involving the transporting of a reaction mixture to which cyanide salt has been added through an electrochemical cell, in which process the cyanide salt reacts with the hydrogen cyanide-reactive compound while at least partly under the influence of an electric current the cyanide salt is acidified and the salt cation content is reduced.

Claims (18)

1. Process comprising the reaction of a cyanide with a hydrogen cyanide-reactive compound, wherein the cyanide is a cyanide salt and the process is an electrochemical process involving the feeding of a reaction mixture to which cyanide salt has been added into an electrochemical cell, in which process the cyanide salt reacts with the hydrogen cyanide-reactive compound, while at least partly under the influence of an electric current the cyanide salt is acidified and the salt cation content is reduced, and wherein the electrochemical process is a membrane water splitting process to produce protons so as to convert water soluble salts into their corresponding acids and bases.

2. The process of claim 1 wherein the electrochemical cell is a bipolar membrane electrodialysis cell.

3. The process of claim 2 wherein the bipolar membrane electrodialysis cell contains bipolar membranes and cation-permeable membranes.

4. The process of claim 2 , wherein only in situ hydrogen cyanide is present, wherein under process conditions the cyanide reacts instantaneously with the hydrogen cyanide-reactive compound.

5. The process of claim 2 , wherein the acidified cyanide salt is present as such for a period of time before it reacts with the hydrogen cyanide-reactive compound in a separate reactor.

6. The process of claim 2 , wherein the hydrogen cyanide-reactive material is an imine-functional condensation product of an amine and aldehyde or ketone, and the product is an aminonitrile.

7. The process of claim 6 , containing an additional step wherein the nitrile is hydrolyzed to a carboxylic acid, an amide or a carboxylate salt.

8. The process of claim 2 , wherein the cyanide salt is an alkali metal cyanide or a mixture of HCN and an alkali metal cyanide.

9. The process of claim 8 , wherein the alkali metal cyanide is sodium cyanide or potassium cyanide.

10. The process of claim 1 , wherein only in situ hydrogen cyanide is present, wherein under process conditions the cyanide reacts instantaneously with the hydrogen cyanide-reactive compound.

11. The process of claim 1 , wherein the acidified cyanide salt is present as such for a period of time before it reacts with the hydrogen cyanide-reactive compound in a separate reactor.

12. The process of claim 1 , wherein the hydrogen cyanide-reactive material is an imine-functional condensation product of an amine and aldehyde or ketone, and the product is an aminonitrile.

13. The process of claim 12 wherein the hydrogen cyanide-reactive material is an imine-functional condensation product of an amino acid and aldehyde or ketone, and the product is an amino acid nitrile.

14. The process of claim 13 containing an additional step wherein the nitrile is hydrolyzed to a carboxylic acid, an amide, or a carboxylate salt.

15. The process of claim 12 containing an additional step wherein the nitrile is hydrolyzed to a carboxylic acid, an amide or a carboxylate salt.

16. The process of claim 1 , wherein the solution in which the process is carried out is an aqueous solution, a solution of organic protic solvents, or a mixture of organic solvents and water.

17. The process of claim 1 , wherein the cyanide salt is an alkali metal cyanide or a mixture of HCN and an alkali metal cyanide.

18. The process of claim 17 , wherein the alkali metal cyanide is sodium cyanide or potassium cyanide.

Assignments (3)
SECURITY INTEREST Recorded Oct 1, 2018
From: STARFRUIT US MERGER SUB 1 LLC; STARFRUIT US MERGER SUB 2 LLC; AKZO NOBEL SURFACE CHEMISTRY LLC; AKZO NOBEL CHEMICALS B.V.; AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: WILMINGTON TRUST (LONDON) LIMITED, AS COLLATERAL AGENT
Reel/Frame 047231/0001 →
CHANGE OF ADDRESS Recorded May 15, 2017
From: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 042745/0406 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 11, 2012
From: APPELMAN, WILHELMUS JOANNES THEODORUS MARIA; LAMMERS, HANS; VOLMER, ARIE; BOONSTRA, TJERK OEDSE; REICHWEIN, ADRIANUS MARIA
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 028350/0802 →