Polyisocyanurate polymers and process for the production of polyisocyanurate polymers

Patent metadata

Field	Value
Publication number	US-11390707-B2
Application number	US-201816010709-A
Country	US
Kind code	B2
Filing date	Jun 18, 2018
Priority date	Apr 21, 2015
Publication date	Jul 19, 2022
Grant date	Jul 19, 2022

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).

First claim

The invention claimed is:

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 .

Assignees

• Covestro Deutschland Ag

Inventors

• Laas Hans-Josef
• Mager Dieter
• Matner Mathias
• Achten Dirk
• Hocke Heiko

Classifications

• C08G18/225

  of alkali or alkaline earth metals · CPC title

• C08G18/092

  oligomerisation to isocyanurate groups · CPC title

• C08G18/3206

  aliphatic · CPC title

• C08G18/027

  the polymeric products containing urethodione groups · CPC title

• C08G18/792

  formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates · CPC title