Catalyst compositions for improving polyurethane foam performance

US10023683B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10023683-B2
Application numberUS-45117606-A
CountryUS
Kind codeB2
Filing dateJun 12, 2006
Priority dateJun 12, 2006
Publication dateJul 17, 2018
Grant dateJul 17, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The present invention provides a reactive catalyst composition for making a water blown flexible polyurethane foam. The catalyst composition comprises one or more tertiary amine catalysts in combination with (1) 2-methyl-1,3-propanediol or (2) a blend of 2-methyl-1,3-propanediol and a C7+ alkanol. The use of such catalyst composition improves the physical properties of the polyurethane foam.

First claim

Opening claim text (preview).

We claim: 1. A method for making a flexible polyurethane foam which comprises contacting a polyisocyanate, with a formulation consisting essentially of: Formulation pbw Polyol  20-100 Silicone Surfactant 0.3-3   water 1-6 Catalyst Composition 0.2-2   and at least one polymer polyol; at least one diluent selected from the group consisting of dipropylene glycol, ethylene glycol and diethylene glycol; and at least one cross-linker selected from the group consisting of diethanolamine, diisopropanolamine, triethanolamine and tripropanolamine; wherein the catalyst composition is 2-methyl-1,3-propanediol and one or more tertiary amine urethane catalysts wherein the amount of 2-methyl-1,3-propanediol is sufficient to achieve a catalyst composition viscosity of 100 to 2000mPa and wherein the polyol includes at least one of polyether and polyester polyols and wherein the polyisocyanate and polyol are provided in amounts such that the isocyanate index is in the range of 70 to 115. 2. The method of claim 1 in which the one or more tertiary amine urethane catalysts are selected from triethylenediamine; 1,8-diaza-bicyclo(5.4.0)undecene-7; quinuclidine; substituted quinuclidines; substituted pyrrolizidines; substituted pyrrolidines; pentamethyldipropylenetriamine; tris(3-dimethylaminopropyl)amine; dimethylcyclohexyl-amine; methyldicyclohexylamine; N,N-dimethylethanolamine; N-alkyl morpholines; dimethylaminopropylamine; N,N,N″,N″-tetramethyldipropylene-triamine; N,N-bis-(3-dimethylaminopropyl)-N-isopropanolamine; N-(3-dimethylamino-propyl)-N,N-diisopropanolamine; 2-(2-dimethylaminoethoxy)ethanol;2-[N-(dimethyl-aminoethyl)-N-methylamino]ethanol; trimethylamine;triethylamine; tributylamine; trioctylamine; diethyl cyclohexylamine; N-methyl-morpholine; N-ethylmorpholine; N-octadecylmorpholine (N-cocomorpholine); N-methyl-diethanolamine; N,N-dimethyl-ethanolamine; N,N′-bis(2-hydroxypropyl)piperazine;N,N,N′,N′-tetramethylethylenediamine; N,N,N′, N′-tetramethyl-1,3-propanediamine; 1,4-bis(2-hydroxypropyI)-2-methylpiperazine; N,N-dimethylbenzylamine; N,N-diethylbenzylamine; N-ethyl-hexamethyleneamine; N-ethylpiperidine; alpha-methyl-benzyldimethylamine; dimethylhexadecylamine; dimethylcetylamine; bisdimethylaminoethyl ether; pentamethyldiethylenetriamine; permethylated polyamines; branched polyamines; 2-[N-(dimethylaminoethoxyethyl)-N-methylamino]ethanol; alkoxylated polyamines; imidazole-borons; aminopropyl-bis(aminoethyl)ethers; 2-dimethylaminoethyl urea; N,N′-bis(2-dimethylaminoethyl) urea; N,N-bis(2-dimethylaminoethyl) urea; 3-dimethyl-aminopropyl urea; N,N′-bis(3-dimethyl-aminopropyl) urea; N,N-bis(3-dimethylamino-propyl) urea; 1-(N-methyl-3-pyrrolidino)-methyl urea; 1,3-bis(N-methyl-3-pyrrolidino)-methyl urea; 3-piperidinopropyl urea; N,N′-bis(3-piperidinopropyl) urea; 2-piperidinoethyl urea; N,N′-bis(2-piperidinoethyl) urea and mixtures thereof. 3. The method of claim 1 in which the one or more tertiary amine urethane catalysts are selected from triethylenediamine; pentamethyldipropylenetriamine; bisdimethylaminoethyl ether; pentamethyldiethylenetriamine; 3-dimethylaminopropyl urea, N,N′-bis(3-dimethyl-aminopropyl) urea, 1-(N-methyl-3-pyrrolidino)methyl urea, 1,3-bis(N-methyl-3-pyrrolidino)methyl urea, and mixtures thereof. 4. The method of claim 1 in which the one or more tertiary amine urethane catalysts are selected from the group consisting of triethylenediamine, bisdimethylaminoethyl ether, or a mixture thereof. 5. The method of claim 1 in which the catalyst composition is 10 to 90wt % one or more tertiary amine catalysts and 90 to 10 wt % 2-methyl-1,3-propanediol component. 6. The method of claim 1 in which the catalyst composition is 25 to 80 wt % tertiary amine catalyst and 75 to 20 wt % 2-methyl-1,3-propanediol. 7. The method of claim 1 in which the catalyst composition is 60 to 90 wt % tertiary amine catalyst and 30 to 10 wt % 2-methyl-1,3-propanediol. 8. The method of claim 1 wherein the relative amounts of the components in the formulation produce a flexible polyurethane foam of 16 to 65 kg/m 3 density, and a tear strength greater than 200 N/m. 9. The method of claim 1 wherein the formulation includes an auxiliary blowing agent. 10. The method of claim 1 wherein the foam also has a Support Factor of about 2.67 as determined by ASTM D-3574 after conditioning for at least seven days at about 23° C. and 50% relative humidity . 11. The method of claim 8 wherein the foam has a Support Factor of about 2.67 as determined by ASTM D-3574 after conditioning for at least seven days at about 23° C. and 50% relative humidity. 12. The method of claim 8 wherein the foam has a Support Factor of about 3.03 as determined by ASTM D-3574 after conditioning for at least seven days at about 23° C. and 50% relative humidity. 13. The method of claim 1 wherein the polyisocyanate comprises toluene diisocyanate. 14. The method of claim 1 wherein the polyisocyanate comprises 4,4′-diphenylmethane diisocyanate. 15. The method of claim 1 wherein the flexible polyurethane foam has a 16 to 65 kg/m 3 density, a tear strength greater than 200N/m and a percent elongation of less than 128%. 16. The method of claim 1 wherein the formulation includes at least one cell stabilizer. 17. The method of claim 4 wherein the one or more tertiary amine urethane catalysts comprises triethylenediamine. 18. The method of claim 1 wherein the amount of 2-methyl-1,3-propanediol is sufficient to increase air flow in the foam. 19. The method of claim 4 wherein the one or more tertiary amine urethane catalyst comprises bisdimethylaminoethyl ether. 20. The method of claim 1 wherein the catalyst composition consists essentially of 2 methyl-1,3-propanediol, triethylenediamine and dimethylaminopropylamine. 21. The method of claim 1 wherein the one or more tertiary amine urethane catalysts are blocked with a carboxylic acid, a phenol or a substituted phenol. 22. The method of claim 1 wherein the polyol consists essentially of polyether polyols. 23. A method for making a polyurethane foam comprising: preparing a catalyst consisting essentially of at least one diluent selected from the group consisting of dipropylene glycol, ethylene glycol and diethylene glycol, at least one tertiary amine catalyst and 2-methyl-1,3-propanediol wherein the catalyst composition has a viscosity of 100-2000 mPa, preparing a pre-mix comprising the catalyst composition, at least one polyether polyol, water and at least one silicone surfactant, contacting the pre-mix with at least one isocyanate under conditions sufficient to produce the foam. 24. The method of claim 23

Assignees

Inventors

Classifications

  • containing oxyethylene end groups · CPC title

  • having ether, acetal, or orthoester groups · CPC title

  • Two or more polyethers of different physical or chemical nature · CPC title

  • being toluene diisocyanate including isomer mixtures · CPC title

  • containing two or more aromatic rings · CPC title

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What does patent US10023683B2 cover?
The present invention provides a reactive catalyst composition for making a water blown flexible polyurethane foam. The catalyst composition comprises one or more tertiary amine catalysts in combination with (1) 2-methyl-1,3-propanediol or (2) a blend of 2-methyl-1,3-propanediol and a C7+ alkanol. The use of such catalyst composition improves the physical properties of the polyurethane foam.
Who is the assignee on this patent?
Bender Jared Denis, Listemann Mark Leo, Tobias James Douglas, and 1 more
What technology area does this patent fall under?
Primary CPC classification C08G18/409. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jul 17 2018 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).