IP Library Granted Patent US 10,131,641
Granted Patent B2
US 10,131,641 · App. 14/774,305 · Granted Nov 20, 2018

Method for producing TDI-trimerisates with high purity

Inventors: Josef Sanders (Leverkusen, DE); Andreas Hecking (Langenfeld, DE); Reinhard Halpaap (Odenthal, DE); Frank Richter (Leverkusen, DE); Oswald Wilmes (Cologne, DE); Jan Busch (Dusseldorf, DE); Tim Loddenkemper (Dormagen, DE); Friedhelm Steffens (Leverkusen, DE); Stefan Groth (Leverkusen, DE)
Assignee: COVESTRO DEUTSCHLAND AG
C07D251/30C08G18/022C08G18/42C08G18/794C09D175/06C09J175/06
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Quick Facts
Patent No.
US 10,131,641
App. No.
14/774,305
Granted
Nov 20, 2018
Kind
B2
Abstract

The invention relates to a novel method for producing polyisocyanurates comprising isocyanate groups, based on 2,4- and 2,6-toluylene diisocyanate (TDI) and to the use thereof in coating compositions.

Claims (12)

1. A method for producing polyisocyanates comprising solvent or diluent and isocyanurate groups, based on 2,4- and/or 2,6-toluylene diisocyanate, having a content of monomeric diisocyanate of <0.5 wt. %, based on polyisocyanate plus solvent, comprising trimerising

A) from 20 to 80 wt. % of a mixture comprising 2,4-toluylene diisocyanate and 2,6-toluylene diisocyanate comprising from 65 to 95 wt. % 2,4-toluylene diisocyanate and from 5 to 35 wt. % 2,6-toluylene diisocyanate in the presence of

B) from 20 to 80 wt. % of solvents or diluents and

C) a phenolic catalyst comprising dialkylaminomethyl groups at a temperature of from 40 to 120° C. to almost complete conversion, and then deactivating the catalyst by addition of an acid-reacting substance or by reaction with an alkylating agent, wherein the toluylene diisocyanate has a content of 2-chloro-6-isocyanato-methylcyclohexadienes (CIMCH) of <5 wt.ppm and wherein the polyisocyanates comprising solvent or diluent and isocyanurate groups have APHA colour indices <100 Hazen.

2. The method according to claim 1 , wherein the toluylene diisocyanate is produced by gas phase phosgenation.

3. The method according to claim 1 , wherein the toluylene diisocyanate has a content of 2-chloro-6-isocyanato-methylcyclohexadienes below the detection limit of 1 wt.ppm.

4. The method according to claim 1 , wherein the catalysts is obtained as Mannich base based on phenol or bisphenol A by reaction with dimethylamine and formaldehyde.

5. The method according to claim 1 , wherein the catalyst is deactivated by dibutyl phosphate or p-toluenesulfonic acid methyl ester.

6. The polyisocyanates produced by the method according to claim 1 comprising solvent or diluent and isocyanurate groups.

7. A method comprising utilizing the polyisocyanate produced according to the method of claim 6 as the polyisocyanate component in polyurethane coatings.

8. The method according to claim 7 wherein the polyisocyanates comprise a crosslinker in two-component polyurethane coatings.

9. A polyurethane adhesive comprising the polyisocyanates produced according to the method of claim 6 .

Assignments (2)
CHANGE OF NAME Recorded Jun 24, 2016
From: BAYER MATERIALSCIENCE AG
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 039153/0556 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 21, 2015
From: SANDERS, JOSEF; HECKING, ANDREAS; HALPAAP, REINHARD; RICHTER, FRANK; WILMES, OSWALD; BUSCH, JAN; LODDENKEMPER, TIM; STEFFENS, FRIEDHELM; GROTH, STEFAN
To: BAYER MATERIALSCIENCE AG
Reel/Frame 036611/0685 →
Priority Claims (1)
EP 13158688 · Mar 12, 2013 · regional
Continuity (1)
Related Publication 20160031834A1 · Feb 4, 2016