Thixotropic polyol compositions containing dispersed urethane-modified polyisocyanurates

US9840579B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9840579-B2
Application numberUS-201414916989-A
CountryUS
Kind codeB2
Filing dateSep 11, 2014
Priority dateSep 13, 2013
Publication dateDec 12, 2017
Grant dateDec 12, 2017

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

Thixotropic polyol dispersions are described. The dispersions contain a dispersed phase of polyurethane-isocyanurate particles. They can be made by reacting a low equivalent weight polyol with a polyisocyanate in the presence of an isocyanate trimerization catalyst while dispersed in a base polyol. These polyol dispersions are useful as the resin component of curable systems such as formulated coatings, sealants or adhesives.

First claim

Opening claim text (preview).

What is claimed is: 1. A thixotropic dispersion of polyurethane-isocyanurate particles in a liquid base polyol, wherein the polyurethane-isocyanurate particles include the reaction product of a polyol having a hydroxyl equivalent weight of up to 80 and 2 to 6 hydroxyl groups per molecule with one or more polyisocyanate compounds in the presence of an isocyanurate trimerization catalyst, and wherein the polyurethane-isocyanurate particles constitute 5 to 35 percent of the weight of the dispersion. 2. The thixotropic dispersion of claim 1 , wherein the liquid base polyol has a hydroxyl equivalent weight of at least 200 and an average nominal hydroxyl functionality of at least two hydroxyl groups per molecule. 3. The thixotropic dispersion of claim 2 , wherein the polyol having a hydroxyl equivalent weight of up to 80 and 2 to 6 hydroxyl groups per molecule includes an aminoalcohol. 4. The thixotropic dispersion of claim 3 , wherein the polyol having a hydroxyl equivalent weight of up to 80 and 2 to 6 hydroxyl groups per molecule is triethanolamine or a mixture containing 75 to 99.9% triethanolamine. 5. The thixotropic dispersion of claim 4 , wherein the polyisocyanate compounds include toluene diisocyanate or MDI. 6. A thixotropic dispersion of polyurethane-isocyanurate particles in a liquid base polyol, wherein the polyurethane-isocyanurate particles include the reaction product of a polyol having a hydroxyl equivalent weight of up to 80 and 2 to 6 hydroxyl groups per molecule with one or more polyisocyanate compounds in the presence of an isocyanurate trimerization catalyst, wherein the particles are multimodal, having at least one fraction having sizes from 20 nm to 1 μm. 7. A thixotropic dispersion of polyurethane-isocyanurate particles in a liquid base polyol, wherein the polyurethane-isocyanurate particles include the reaction product of a polyol having a hydroxyl equivalent weight of up to 80 and 2 to 6 hydroxyl groups per molecule with one or more polyisocyanate compounds in the presence of an isocyanurate trimerization catalyst, which thixotropic dispersion has a viscosity of at least 100 Pa·s at 20° C., as measured using a Bohlin rheometer with cone-and-plate geometry, operated in a rotational mode at 20° C. at a speed of one Hz. 8. A method of making the thixotropic dispersion of claim 1 , comprising reacting a polyol having an equivalent weight of up to 80 and 2 to 6 hydroxyl groups per molecule with one or more polyisocyanate compounds in the presence of an isocyanurate trimerization catalyst and a base polyether polyol having a hydroxyl equivalent weight of at least 200 to form polyurethane-isocyanurate particles dispersed in the base polyol, where the reacting step is performed in the presence of a prepolymer that contains isocyanate or isocyanate-reactive groups. 9. A method of making the thixotropic dispersion of claim 1 , comprising reacting a polyol having an equivalent weight of up to 80 with one or more polyisocyanate compounds in the presence of an isocyanurate trimerization catalyst, a prepolymer that has isocyanurate groups and isocyanate or isocyanate-reactive groups and a base polyether polyol to form polyurethane-isocyanurate particles dispersed in the base polyol. 10. A curable resin composition comprising the thixotropic dispersion of claim 1 and at least one curing agent that reacts with hydroxyl groups. 11. The curable resin composition of claim 10 which is a formulated coating, formulated sealant or formulated adhesive. 12. The thixotropic dispersion of claim 6 , wherein the liquid base polyol has a hydroxyl equivalent weight of at least 200 and an average nominal hydroxyl functionality of at least two hydroxyl groups per molecule. 13. The thixotropic dispersion of claim 12 , wherein the polyol having a hydroxyl equivalent weight of up to 80 and 2 to 6 hydroxyl groups per molecule includes an aminoalcohol. 14. The thixotropic dispersion of claim 13 , wherein the polyol having a hydroxyl equivalent weight of up to 80 and 2 to 6 hydroxyl groups per molecule is triethanolamine or a mixture containing 75 to 99.9% triethanolamine. 15. The thixotropic dispersion of claim 14 , wherein the polyisocyanate compounds include toluene diisocyanate or MDI. 16. The thixotropic dispersion of claim 7 , wherein the liquid base polyol has a hydroxyl equivalent weight of at least 200 and an average nominal hydroxyl functionality of at least two hydroxyl groups per molecule. 17. The thixotropic dispersion of claim 16 , wherein the polyol having a hydroxyl equivalent weight of up to 80 and 2 to 6 hydroxyl groups per molecule includes an aminoalcohol. 18. The thixotropic dispersion of claim 17 , wherein the polyol having a hydroxyl equivalent weight of up to 80 and 2 to 6 hydroxyl groups per molecule is triethanolamine or a mixture containing 75 to 99.9% triethanolamine. 19. The thixotropic dispersion of claim 18 , wherein the polyisocyanate compounds include toluene diisocyanate or MDI. 20. A curable resin composition comprising the thixotropic dispersion of claim 6 and at least one curing agent that reacts with hydroxyl groups. 21. The curable resin composition of claim 20 which is a formulated coating, formulated sealant or formulated adhesive. 22. A curable resin composition comprising the thixotropic dispersion of claim 7 and at least one curing agent that reacts with hydroxyl groups. 23. The curable resin composition of claim 22 which is a formulated coating, formulated sealant or formulated adhesive.

Assignees

Inventors

Classifications

  • Compounds containing ether groups, e.g. oxyalkylated monohydroxy compounds · CPC title

  • of alkali or alkaline earth metals · CPC title

  • Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step · CPC title

  • containing oxypropylene or higher oxyalkylene end groups · CPC title

  • the dispersing or dispersed phase being a polyol · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9840579B2 cover?
Thixotropic polyol dispersions are described. The dispersions contain a dispersed phase of polyurethane-isocyanurate particles. They can be made by reacting a low equivalent weight polyol with a polyisocyanate in the presence of an isocyanate trimerization catalyst while dispersed in a base polyol. These polyol dispersions are useful as the resin component of curable systems such as formulated …
Who is the assignee on this patent?
Dow Global Technologies Llc
What technology area does this patent fall under?
Primary CPC classification C08G18/7621. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Dec 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).