IP Library Granted Patent US 8,445,623
Granted Patent B2
US 8,445,623 · App. 12/861,306 · Granted May 21, 2013

Process for the preparation of polyisocyanates with a biuret structure

Inventors: Martin Brahm (Odenthal, DE); Dieter Mager (Leverkusen, DE); André Fellhoelter (Bergisch Gladbach, DE); Reinhard Halpaap (Odenthal, DE)
Assignee: Bayer MaterialScience AG
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Quick Facts
Patent No.
US 8,445,623
App. No.
12/861,306
Granted
May 21, 2013
Kind
B2
Abstract

The present invention relates to an improved process for the preparation of polyisocyanates with a biuret structure by continuous reaction of excess amounts of organic diisocyanates having exclusively aliphatically and/or cycloaliphatically bonded isocyanate groups with organic diamines having exclusively aliphatically and/or cycloaliphatically bonded primary amino groups at elevated temperatures by 2-stage addition of the isocyanate component.

Claims (17)

1. A process for continuously preparing a polyisocyanate comprising a biuret structure comprising continuously reacting an excess amount of an organic isocyanate (A) comprising exclusively aliphatically and/or cycloaliphatically bonded isocyanate groups with an organic amine (B) comprising exclusively aliphatically and/or cycloaliphatically bonded primary amino groups by

a) mixing a first amount of said organic isocyanate (A) with said organic amine (B) at a temperature above 170° C. to form a reaction mixture stream, and

b) metering a second amount of said organic isocyanate (A) at a temperature in the range of from 20 to 250° C. into said reaction mixture stream of a),

wherein

the ratio of the parts by weight of said organic isocyanate (A) fed per unit time into step a) to the parts by weight of said organic isocyanate (A) fed per unit time into b) is in the range of from 1:9 to 9:1, and

the ratio of the total number of NCO groups fed per unit time into both steps a) and b) to the number of NH 2 groups fed in per unit time into step a) is at least 4:1.

2. The process of claim 1 , wherein said organic isocyanate (A) comprises HDI.

3. The process of claim 1 , wherein said organic amine (B) comprises HDA.

4. The process of claim 1 , wherein the ratio of the total number of NCO groups fed per unit time into both steps a) and b) to the number of NH 2 groups fed in per unit time into step a) is in the range of from 18:1 to 25:1.

5. The process of claim 1 , wherein the ratio of the parts by weight of said organic isocyanate (A) fed per unit time into step a) to the parts by weight of said organic isocyanate (A) fed per unit time into b) is in the range of from 5:5 to 7.5:2.5.

6. The process of claim 1 , wherein said first amount of said organic isocyanate (A) in step a) is preheated to a temperature in the range of from 200 to 240° C. before it is mixed with said organic amine (B).

7. The process of claim 1 , wherein the temperature in step a) is maintained in the range of from 230 to 320° C.

8. The process of claim 1 , wherein said second amount of said organic isocyanate (A) in step b) has a temperature below that of said first amount of said organic isocyanate (A) in step a).

9. The process of claim 1 , wherein said process is carried in the presence of a catalyst.

10. The process of claim 9 , wherein said catalyst comprises one or more acids or mixtures thereof.

11. The process of claim 10 , wherein said catalyst comprises di-n-butyl phosphate.

12. The process of claim 1 , wherein said polyisocyanate comprising a biuret structure is purified from excess monomeric diisocyanate via extraction or thin film distillation resulting in a monomeric diisocyanate content of less than 0.5 wt. %.

Assignments (2)
CHANGE OF NAME Recorded Mar 30, 2016
From: BAYER MATERIALSCIENCE AG
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 038399/0469 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 19, 2010
From: BRAHM, MARTIN; MAGER, DIETER; FELLHOLTER, ANDRE; HALPAAP, REINHARD
To: BAYER MATERIALSCIENCE AG
Reel/Frame 025158/0650 →
Priority Claims (1)
DE 10 2009 038 463 · Aug 21, 2009 · national
Continuity (1)
Related Publication 20110046300A1 · Feb 24, 2011