IP Library Granted Patent US 9,440,937
Granted Patent B2
US 9,440,937 · App. 14/359,125 · Granted Sep 13, 2016

Method for producing polyisocyanates and use thereof

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Quick Facts
Patent No.
US 9,440,937
App. No.
14/359,125
Granted
Sep 13, 2016
Kind
B2
Abstract

The invention relates to a method for modifying isocyanates using catalysts having a water content not exceeding 1,000 ppm.

Claims (11)

1. A method for preparing polyisocyanates comprising iminooxadiazinedione groups by oligomerization of monomeric di- and/or triisocyanates comprising utilizing a catalyst, wherein the catalyst is a quaternary phosphonium polyfluoride of the formula R 4 P + F − .n(HF), where R are the same or different, optionally branched, aliphatic, aromatic and/or araliphatic C 1 -C 20 residues and optionally two or more substituents R may also form saturated or unsaturated rings with one another and with the phosphorus atom and n can have any values between 0.1 and 20, and wherein the water content of the catalyst added to the isocyanates to be oligomerized does not exceed 1000 ppm.

2. A method for preparing polyisocyanates containing iminooxadiazinedione groups which comprises reacting

a) at least one organic di- and/or triisocyanate,

b) one or more catalyst, comprising at least one quaternary phosphonium polyfluoride wherein the water contents of the catalyst does not exceed 1000 ppm in total,

c) optionally a solvent and

d) optionally an additive.

3. The method as claimed in claim 2 , wherein the method is carried out in the temperature range between 0° C. and 250° C.

4. The method as claimed in claim 2 , wherein the method is interrupted after 5 to 80% of the monomeric diisocyanate used have reacted.

5. The method as claimed in claim 2 , wherein the catalyst is used in a proportion between 1 mol ppm and 1 mol %, based on the amount of monomer.

6. The method as claimed in claim 2 , wherein unreacted monomer is removed from the reaction mixture.

7. The method as claimed in claim 2 , wherein at least one isocyanate used in the method is selected from the group consisting of hexamethylene diisocyanate (HDI), 2-methylpentane-1,5-diisocyanate, 2,4,4-trimethyl-1,6-hexanediisocyanate, 2,2,4-trimethyl-1,6-hexanediisocyanate, 4-isocyanatomethyl-1,8-octanediisocyanate, 3(4)-isocyanatomethyl-1-methylcyclohexyl isocyanate (IMCI), isophorone diisocyanate (IPDI), 1,3- and 1,4-bis(isocyanatomethyl)benzene (XDI), 1,3- and 1,4-bis(isocyanatomethyl)cyclohexane (H6XDI), 2,4- and 2,6-toluylene diisocyanate (TDI), bis(4-isocyanatophenyl)methane (4,4′MDI), 4-isocyanatophenyl-2-isocyanatophenylmethane (2,4′MDI), and polycyclic products which are accessible by formaldehyde-aniline polycondensation and subsequent conversion of the resulting (poly)amines to the corresponding (poly)isocyanates (polymer-MDI).

Assignments (4)
CHANGE OF NAME Recorded Apr 7, 2016
From: BAYER MATERIALSCIENCE AG
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 038374/0844 →
CHANGE OF NAME Recorded Mar 21, 2016
From: BAYER MATERIALSCIENCE AG
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 038188/0408 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2016
From: BAYER INTELLECTUAL PROPERTY GMBH
To: BAYER MATERIALSCIENCE AG
Reel/Frame 038056/0732 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2015
From: RICHTER, FRANK; BRAHM, MARTIN
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 035445/0731 →