IP Library Granted Patent US 7,501,045
Granted Patent B2
US 7,501,045 · App. 10/565,483 · Granted Mar 10, 2009

Method of producing and separating dinitrile compounds

Assignee: Rhodia Polyamide Intermediates
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Quick Facts
Patent No.
US 7,501,045
App. No.
10/565,483
Granted
Mar 10, 2009
Kind
B2
Abstract

The present invention relates to a process for the manufacture and separation of dinitrile compounds. It relates more particularly to a process for the manufacture and separation of dinitrile compounds from a medium originating from the hydrocyanation of unsaturated mononitriles. The invention consists in feeding the medium comprising the dinitriles to a distillation column and then recovering the purified dinitriles as intermediate fraction, the heavy products being removed as column tail fraction and the light products, including the unsaturated mononitriles, being recovered as top fraction.

Claims (25)

1. A process for the manufacture and separation of dinitriles from a medium originating from a hydrocyanation of unsaturated mononitriles, comprising the steps of:

a) feeding the medium comprising the dinitriles to a distillation column,

b) recovering, at the column top, compounds with a lower boiling point than that of the dinitriles,

c) recovering an intermediate fraction comprising the dinitriles from a theoretical plate situated in a lower part of the column with respect to a feed point of the medium comprising the dinitriles, and

d) recovering, at the column bottom, products with a higher boiling point than that of the dinitriles,

wherein the recovery of the intermediate fraction is carried out either without reflux or with reflux with a reflux ratio of between 1 and 6% by weight of the intermediate fraction.

2. The process according to claim 1 , wherein the column bottom is at a temperature of less than 200° C., optionally between 140° C. and 190° C.

3. The process according to claim 1 , wherein the dinitrile compounds are compounds of following general formula (I):

NC—R—CN   (I)

in which the R radical represents a saturated hydrocarbonaceous radical having from 2 to 10 carbon atoms.

4. The process according to claim 3 , wherein the dinitriles are adiponitrile, methylglutaronitrile or ethylsuccinonitrile.

5. The process according to claim 1 , wherein said process is carried out under a pressure of between 1 kPa and 5 kPa.

6. The process according to claim 1 , wherein the distillation column is a plate column, a packed column or a partition column.

7. A process for the manufacture and separation of dinitriles from a medium originating from a hydrocyanation of unsaturated mononitriles, comprising the steps of:

a) feeding the medium comprising the dinitriles to a distillation column,

b) recovering, at the column top, compounds with a lower boiling point than that of the dinitriles,

c) recovering an intermediate fraction comprising the dinitriles from a theoretical plate situated in a lower part of the column with respect to a feed point of the medium comprising the dinitriles, and

d) recovering, at the column bottom, products with a higher boiling point than that of the dinitriles,

wherein the recovery of the intermediate fraction is carried out without reflux.

8. A process for the manufacture and separation of dinitriles from a medium originating from a hydrocyanation of unsaturated mononitriles, comprising the steps of:

a) feeding the medium comprising the dinitriles to a distillation column,

b) recovering, at the column top, compounds with a lower boiling point than that of the dinitriles,

c) recovering an intermediate fraction comprising the dinitriles from a theoretical plate situated in a lower part of the column with respect to a feed point of the medium comprising the dinitriles, and

d) recovering, at the column bottom, products with a higher boiling point than that of the dinitriles,

wherein the recovery of the intermediate fraction is carried out with a reflux ratio of between 1 and 6% by weight of the intermediate fraction.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 7, 2021
From: INVISTA NORTH AMERICA, LLC
To: INV NYLON CHEMICALS AMERICAS, LLC
Reel/Frame 054914/0897 →
CHANGE OF NAME Recorded Dec 15, 2020
From: INVISTA NORTH AMERICA S.A.R.L.
To: INVISTA NORTH AMERICA, LLC
Reel/Frame 054765/0645 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 27, 2014
From: RHODIA OPERATIONS
To: INVISTA NORTH AMERICA SARL
Reel/Frame 033194/0666 →
CHANGE OF NAME Recorded Mar 4, 2014
From: RHODIA POLYAMIDE INTERMEDIATES
To: RHODIA OPERATIONS
Reel/Frame 032385/0429 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 20, 2006
From: GERBER, JEROME; LECONTE, PHILIPPE; AMOROS, DANIEL
To: RHODIA POLYAMIDE INTERMEDIATES
Reel/Frame 017494/0794 →
Priority Claims (1)
FR 03 09152 · Jul 25, 2003 · national
Continuity (1)
Related Publication 20060175189A1 · Aug 10, 2006