IP Library Granted Patent US 11,390,707
Granted Patent B2
US 11,390,707 · App. 16/010,709 · Granted Jul 19, 2022

Polyisocyanurate polymers and process for the production of polyisocyanurate polymers

Inventors: Hans-Josef Laas (Odenthal, DE); Dieter Mager (Leverkusen, DE); Mathias Matner (Neuss, DE); Dirk Achten (Leverkusen, DE); Heiko Hocke (Shanghai, CN)
Assignee: Covestro Deutschland AG
C08G18/022C08G18/027C08G18/792C07D251/34
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Quick Facts
Patent No.
US 11,390,707
App. No.
16/010,709
Granted
Jul 19, 2022
Kind
B2
Abstract

The present invention relates to novel polyisocyanurate plastics which are obtainable by catalytic trimerization of a polyisocyanate composition A) which contains oligomeric polyisocyanates and is low in monomeric diisocyanates. “Low in monomeric diisocyanates” means that the polyisocyanate composition A) has a content of monomeric diisocyanates of at most 20% by weight. The invention further relates to the use of these polyisocyanurate plastics for production of coatings, films, semi-finished products and mouldings, and to a process for producing polyisocyanurate plastics comprising the following steps: (a) providing a polyisocyanate composition A) which contains oligomeric polyisocyanates and is low in monomeric diisocyanates, “low in monomeric diisocyanates” meaning that the polyisocyanate composition A) has a content of monomeric diisocyanates of at most 20% by weight; (b) catalytically trimerizing the polyisocyanate composition A).

Claims (12)

1. A polyisocyanurate plastic obtainable by catalytic trimerization of a polyisocyanate composition A) having a content of isocyanate groups of 8.0% to 28.0% by weight, consisting of at least 70 wt.-% based on its weight of polyisocyanates having exclusively aliphatically and/or cycloaliphatically bonded isocyanate groups and which contains at least 50% of oligomeric polyisocyanates structure selected from the group consisting of uretdione, isocyanurate, biuret, iminooxadiazinedione and oxadianzinetrione and is low in monomeric diisocyanates, wherein low in monomeric diisocyanates means that the polyisocyanate composition A) has a content of monomeric diisocyanates of at most 20% by weight, and wherein at most 10% of the isocyanate groups originally present in the polyisocyanate composition A) have been conserved, and wherein the polyisocyanate composition A) is free of allophanate groups.

2. The polyisocyanurate plastic according to claim 1 , wherein the oligomeric polyisocyanates are selected from at least one oligomeric polyisocyanate having uretdione, isocyanurate, biuret, iminooxadiazinedione or oxadiazinetrione structure or mixtures thereof but are essentially free of allophanate structures.

3. The polyisocyanurate plastic according to claim 1 , wherein the oligomeric polyisocyanates are a mixture of at least two oligomeric polyisocyanates, where the at least two oligomeric polyisocyanates are of different structure selected from the group consisting of uretdione, isocyanurate, biuret, iminooxadiazinedione and oxadiazinetrione structure and mixtures thereof.

4. The polyisocyanurate plastic according to claim 1 , wherein the polyisocyanate composition A) consists to an extent of at least 90% by weight, based on the weight of the polyisocyanate composition A), of polyisocyanates having exclusively aliphatically and/or cycloaliphatically bonded isocyanate groups.

5. The polyisocyanurate plastic according to claim 1 , wherein the polyisocyanate composition A) consists to an extent of at least 99% by weight, based on the weight of the polyisocyanate composition A), of polyisocyanates having exclusively aliphatically and/or cycloaliphatically bonded isocyanate groups.

6. The polyisocyanurate plastic according to claim 1 , wherein the oligomeric polyisocyanates have exclusively aliphatically and/or cycloaliphatically bonded isocyanate groups.

7. The polyisocyanurate plastic according to claim 1 , wherein the oligomeric polyisocyanates consist of one or more oligomeric polyisocyanates formed from 1,5-diisocyanatopentane, 1,6-diisocyanatohexane, isophorone diisocyanate or 4,4′-diisocyanatodicyclohexylmethane or mixtures thereof.

8. The polyisocyanurate plastic according to claim 1 , wherein the polyisocyanate composition A) and/or the oligomeric polyisocyanates have/has a mean NCO functionality of 2.0 to 5.0.

9. The polyisocyanurate plastic according to claim 1 , wherein “low in monomeric diisocyanates” means that the polyisocyanate composition A) has a content of monomeric diisocyanates of not more than 15% by weight, based on the weight of the polyisocyanate composition A).

10. The polyisocyanurate plastic according to claim 1 , wherein said low in monomeric diisocyanates means that the polyisocyanate composition A) has a content of monomeric diisocyanates of not more than 5% by weight, based on the weight of the polyisocyanate composition A).

11. The polyisocyanurate plastic according to claim 1 , wherein the polyisocyanate composition A) is obtainable by modifying monomeric diisocyanates with subsequent removal of unconverted monomers.

12. Coatings, films, semi-finished products and mouldings comprising the polyisocyanurate plastic according to claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 18, 2018
From: LAAS, HANS-JOSEF; MAGER, DIETER; MATNER, MATHIAS; ACHTEN, DIRK; HOCKE, HEIKO
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 046117/0476 →
Priority Claims (1)
EP 15164520 · Apr 21, 2015 · regional
Continuity (2)
Continuation 15568110
Related Publication 20180355091A1 · Dec 13, 2018
Cited By (1)
US 12,594,700