Thermoplastic polyurethanes made with tin-free catalysts

US2016237197A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016237197-A1
Application numberUS-201415028084-A
CountryUS
Kind codeA1
Filing dateOct 10, 2014
Priority dateOct 15, 2013
Publication dateAug 18, 2016
Grant date

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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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  6. CPC / IPC classifications

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Abstract

Official abstract text for this publication.

Thermoplastic polyurethanes, including those based on aliphatic isocyanates, are of great interest for industrial applications that require UV-stability. To overcome the low reactivity of some diisocyanates a catalyst is usually added to accelerate urethane formation. In most applications, organotin-based compounds are used, however, due to growing concerns about the toxicity of some of these organotin compounds, their use is being restricted and the need for alternative catalysts is growing. The thermoplastic polyurethanes described herein are made using tin-free catalysts while retaining the UV-stability and other properties required for many industrial applications.

First claim

Opening claim text (preview).

1 . A thermoplastic polyurethane composition comprising the reaction product of: a) a polyisocyanate; b) a polyol component; and c) a chain extender component; wherein the reaction is carried out in the presence of a catalyst; wherein said catalyst comprises one or more iron compounds. 2 . The thermoplastic polyurethane composition of claim 1 wherein the catalyst is free of tin. 3 . The thermoplastic polyurethane composition of claim 1 wherein the catalyst comprises a compound having the general structure (X) m -M-(Y) n where m is 2 or 3, M is iron; each X is independently a ligand with a −1 charge, obtained by deprotonation of a β-diketone compound, a β-ketoester compound, a β-ketoamide compound or any other β-dicarbonyl compound, chloride, bromide, iodide, fluoride, perchlorate, alkoxide, alkylsulfonate, arylsulfonate, alkylsulfate, arylsulfate, hydroxide, or a combination of these ligands; each Y is a neutral ligand; and n is an integer between 0 and 6. 4 . The thermoplastic polyurethane composition of claim 1 wherein the catalyst comprises a compound of Fe(III) or Fe(II) containing three or two anionic ligands, each formed by deprotonation of a β-diketone, a β-ketoester, a β-ketoamide, or a combination thereof. 5 . The thermoplastic polyurethane composition of claim 1 wherein the catalyst comprises a compound of Fe(III) or Fe(II) containing three or two halide counteranions each derived from chloride, fluoride, bromide, iodide, a compound resulting from the partial alcoholysis or hydrolysis of any of these compounds, or a combination thereof. 6 . The thermoplastic polyurethane composition of claim 1 wherein the catalyst comprises a compound of Fe(III) or Fe(II) containing one, two or three α-diimine ligands each derived from 2,2′-bipyridine, 1,10-phenanthroline, substituted variants of 2,2′-bipyridine or 1,10-phenanthroline, or some combination thereof. 7 . The thermoplastic polyurethane composition of claim 1 wherein the catalyst comprises iron(III)-tris-2,4-pentanedionate, iron(III)-tris-(1,1,1-trifluoro-2,4-pentanedionate), iron(III)-tris-(1,1,1,5,5,5-hexafluoro-2,4-pentanedionate), iron (III)-tris-(2,2,6,6-tetramethyl-3,5-heptanedionate), iron(III)-tris-(6-methyl-2,4-heptanedionate); iron (III) chloride, iron(II)chloride, iron(III)bromide; iron(III)-tris(2,2′-bipyridine) trichloride, iron(III)-tris(1,10-phenanthroline) trichloride, or combinations thereof. 8 . The thermoplastic polyurethane composition of claim 1 wherein the polyisocyanate comprises an aromatic diisocyanate, an aliphatic diisocyanate, or a combination thereof. 9 . The thermoplastic polyurethane composition of claim 1 wherein the polyisocyanate is at least 50%, on a weight basis, a cycloaliphatic diisocyanate. 10 . The thermoplastic polyurethane composition of claim 1 wherein the polyol component comprises a polyether polyol. 11 . The thermoplastic polyurethane composition of claim 1 wherein the chain extender component comprises diols, diamines, or combinations thereof. 12 . The thermoplastic polyurethane composition of claim 1 wherein the polyisocyanate comprises 4,4′-methylene bis(cyclohexylisocyanate); wherein the polyol component comprises poly(tetramethylene ether glycol); wherein the chain extender component comprises 1,4-butanediol; and wherein the catalyst comprises iron (III) chloride. 13 . A process of preparing a thermoplastic polyurethane composition comprising the step of: (I) reacting: a) a polyisocyanate; b) a polyol component; and c) a chain extender component; wherein the reaction is carried out in the presence of a catalyst; wherein said catalyst comprises one or more iron (III) compounds; resulting in a thermoplastic polyurethane composition. 14 . An article comprising the thermoplastic polyurethane composition of claim 1 . 15 . A method of maintaining the ultraviolet stability of a thermoplastic polyurethane composition while reducing the toxicity of the thermoplastic polyurethane composition, comprising the steps of: (I) reacting: a) a polyisocyanate; b) a polyol component; and c) a chain extender component; wherein the reaction is carried out in the presence of a catalyst; wherein said catalyst comprises one or more iron (III) compounds; resulting in a thermoplastic polyurethane composition with ultraviolet stability and reduced toxicity compared to a similar thermoplastic polyurethane composition made using a tin containing catalyst

Assignees

Inventors

Classifications

  • containing two or more cycloaliphatic rings · CPC title

  • C08G18/222Primary

    metal compounds not provided for in groups C08G18/225 - C08G18/26 · CPC title

  • with compounds of group C08G18/3203 · CPC title

  • Polyurethanes · CPC title

  • Environmental burden or human safety, e.g. CO2 footprint, fuming or leaching · CPC title

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What does patent US2016237197A1 cover?
Thermoplastic polyurethanes, including those based on aliphatic isocyanates, are of great interest for industrial applications that require UV-stability. To overcome the low reactivity of some diisocyanates a catalyst is usually added to accelerate urethane formation. In most applications, organotin-based compounds are used, however, due to growing concerns about the toxicity of some of these o…
Who is the assignee on this patent?
Lubrizol Advanced Mat Inc
What technology area does this patent fall under?
Primary CPC classification C08G18/222. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Aug 18 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). 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).