Synthesis and use of metallized polyhedral oligomeric silsesquioxane catalyst compositions

US9822210B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9822210-B2
Application numberUS-201415032662-A
CountryUS
Kind codeB2
Filing dateAug 7, 2014
Priority dateOct 28, 2013
Publication dateNov 21, 2017
Grant dateNov 21, 2017

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Abstract

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The present invention relates to a method to form a polyurethane material, a catalyst composition comprising metalized polyhedral oligomeric silsesquioxanes (POMS) compounds in combination with reactive compounds suitable to be used to provide a polyurethane material and the polyurethane material obtained using the catalyst composition.

First claim

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The invention claimed is: 1. A method to form a polyurethane material, the method comprises the steps of: providing at least one isocyanate; providing at least one isocyanate reactive component; providing a catalyst composition comprising metalized polyhedral oligomeric silsesquioxanes (POMS) compounds wherein: said POMS compounds are reaction products of metallic alkoxides and silsesquioxane silanols corresponding to structure [2], and the number of equivalents of silsesquioxane silanols used is higher than the number of equivalents of metallic alkoxides used to react with said silsesquioxane silanols, R is selected from an alkyl group comprising 1 to 20 carbon atoms; and blending said at least one isocyanate, at least one isocyanate reactive component and said catalyst composition to form a blend and reacting said blend to provide said polyurethane material. 2. The method according to claim 1 wherein the metal in the metallic alkoxide in the catalyst composition is selected from a 4 and/or 5 coordinated metal which is selected from s, p, d, f, block metals. 3. The method according to claim 2 , wherein the metal is selected from the group consisting of Ti, Zr, B, Al, and Sn. 4. The method according to claim 2 , wherein the metallic alkoxide compound is titanium tetra alkoxide. 5. The method according to claim 1 wherein the ratio of the number of equivalents of silsesquioxane silanols over the number of equivalents of metallic alkoxides is in the range 1.5:1 up to 2:1. 6. The method according to claim 1 wherein the catalyst composition is a mixture comprising following intermediate POMS structures [8], [9], [10] and [11] in a dynamic equilibrium: wherein R is selected from an alkyl group comprising 1 to 20 carbon atoms. 7. The method according to claim 1 , wherein said metallized polyhedral oligomeric silsesquioxane is incorporated into an isocyanate reactive component before blending said at least one isocyanate, at least one isocyanate reactive component and said catalyst composition. 8. The method according to claim 1 , wherein the isocyanate reactive component comprises monools, polyols, or combinations thereof. 9. The method according to claim 1 , wherein the isocyanate reactive component is selected from monools or polyols which have an average nominal hydroxy functionality of 1-8 and an average molecular weight of 32-8000. 10. The method according to claim 1 , wherein the isocyanate reactive component comprises methanol, ethanol, propanol, butanol, phenol, cyclohexanol, hydrocarbon monools having an average molecular weight of 200-5000, ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, tripropylene glycol, trimethylol propane, sorbitol, sucrose, glycerol, ethanediol, propanediol, butanediol, pentanediol, hexanediol, aromatic polyols having a molecular weight of up to 8000, aliphatic polyols having a molecular weight of up to 8000, polyester polyols having an average molecular weight of 200-8000, polyether polyester polyols having an average molecular weight of 200-8000, polyether polyols having an average molecular weight of 200-8000, or combinations thereof. 11. The method according to claim 1 , wherein the blending of said at least one isocyanate, at least one isocyanate reactive component and said catalyst composition is done at a temperature between −10° C. and 25° C. 12. The method according to claim 1 , wherein said blend of said at least one isocyanate, at least one isocyanate reactive component and said metallized polyhedral oligomeric silsesquioxane is brought to a temperature between 25° C. and 200° C. to initiate the reaction of said at least one isocyanate, at least one isocyanate reactive component and said catalyst composition. 13. The method according to claim 1 , wherein at least one gelling catalyst is provided to said blend of said at least one isocyanate, at least one isocyanate reactive component and said catalyst composition. 14. The method according to claim 1 , wherein at least one blowing catalyst is provided to said blend of said at least one isocyanate, at least one isocyanate reactive component and said catalyst composition. 15. The method according to claim 1 wherein the concentration of said metallized polyhedral oligomeric silsesquioxane in said blend of said at least one isocyanate, at least one isocyanate reactive component and said catalyst composition is less than or equal to 10 mM. 16. A reactive composition, said reactive composition comprising: at least one isocyanate compound; at least one isocyanate reactive component; a catalyst composition according to claim 1 .

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What does patent US9822210B2 cover?
The present invention relates to a method to form a polyurethane material, a catalyst composition comprising metalized polyhedral oligomeric silsesquioxanes (POMS) compounds in combination with reactive compounds suitable to be used to provide a polyurethane material and the polyurethane material obtained using the catalyst composition.
Who is the assignee on this patent?
Huntsman Int Llc
What technology area does this patent fall under?
Primary CPC classification C08G18/22. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Nov 21 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).