IP Library Granted Patent US 8,399,658
Granted Patent B2
US 8,399,658 · App. 12/951,289 · Granted Mar 19, 2013

Method for isolation of laurolactam from a laurolactam synthesis process stream

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Quick Facts
Patent No.
US 8,399,658
App. No.
12/951,289
Granted
Mar 19, 2013
Kind
B2
Abstract

A process for purifying laurolactam by means of integrated connection of distillation and crystallization is provided. The crystallization is performed as a solution or melt crystallization. The process reduces thermal stress applied to the laurolactam stream and improved yields are obtained. Raw materials are recovered and recycled in the production sequence.

Claims (38)

1. A method for isolation and purification of laurolactam from a laurolactam synthesis process stream, comprising:

cooling the synthesis process stream comprising laurolactam, a mother liquor, synthesis starting materials and low, mid- and high boiling fractions to a temperature wherein only a solubility limit of the laurolactam is exceeded, to selectively crystallize the laurolactam from the mother liquor;

separating the crystallized laurolactam from the mother liquor in a downstream solid-liquid separation; and

sending the mother liquor from which the crystallized laurolactam is separated to a multistage distillation sequence;

wherein components of the laurolactam synthesis process stream are recovered.

2. The process according to claim 1 , wherein

the selective crystallization is a solution crystallization.

3. The process according to claim 2 , wherein

the solution crystallization is a solution cooling crystallization.

4. The process according to claim 3 , wherein

the solution cooling crystallization comprises a flash cooling crystallization.

5. The process according to claim 1 , wherein

the selective crystallization and separation remove more than 80% of the laurolactam in the laurolactam synthesis process stream from the stream.

6. The process according to claim 1 , further comprising:

washing the separated crystallized laurolactam with a wash liquid to remove mother liquor adhering to the crystallized laurolactam.

7. The process according to claim 6 , wherein

the wash liquid comprises at least one selected from the group consisting of hydrocumene, cyclododecanone, cyclododecatriene, toluene, cycloheptane, cyclooctane, cyclononane, cyclodecane, cyclododecane, vinylcyclohexane, ethylcyclohexane, dimethylcyclohexane and tert-butylcyclohexane.

8. The process according to claim 6 ,

wherein the wash liquid is hydrocumene.

9. The process according to claim 1 , further comprising:

drying the separated crystallized laurolactam.

10. The process according to claim 3 , wherein

a purity of the separated crystallized laurolactam is greater than 99%.

11. The process according to claim 1 , further comprising:

distilling the synthesis process stream comprising laurolactam before the cooling to a temperature where only a solubility limit of the laurolactam is exceeded.

12. The process according to claim 11 , wherein

the distillation of the synthesis process stream comprises:

a distillative separating sequence in which the low boilers present are distilled overhead with solvent, and bottoms from the low boiler column which comprise laurolactam are treated as the synthesis process stream.

13. The process according to claim 12 , wherein

the crystallization is a solution cooling crystallization.

14. The process according to claim 13 , wherein

the solution cooling crystallization is a flash cooling crystallization.

15. A method for isolation of laurolactam from a laurolactam synthesis process stream, comprising:

increasing the temperature of the synthesis process stream comprising laurolactam, a mother liquor, synthesis starting materials and low, mid- and high boiling fractions by conducting the synthesis process stream through a heat exchanger;

decompressing the heated synthesis process stream in a flash vessel to obtain a vapor phase and a low-boiling fraction which comprises laurolactam;

sending the vapor phase to a distillative separating sequence to produce a fraction of the vapor phase comprising laurolactam;

combining the low-boiling fraction and the vapor phase fraction comprising laurolactam; and

melt crystallizing the combined fractions.

Assignments (2)
CHANGE OF NAME Recorded Jan 31, 2020
From: EVONIK DEGUSSA GMBH
To: EVONIK OPERATIONS GMBH
Reel/Frame 051765/0166 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 31, 2011
From: HENGSTERMANN, AXEL; MEIER, RALF; DEMICOLI, DANIEL; ROOS, MARTIN; GUENZEL, BERND; HUEBNER, FRANK
To: EVONIK DEGUSSA GMBH
Reel/Frame 025723/0750 →