Polyurethane elastomers made using mixtures of aliphatic diol chain extender and secondary amine
US-9221941-B2 · Dec 29, 2015 · US
US2016237197A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016237197-A1 |
| Application number | US-201415028084-A |
| Country | US |
| Kind code | A1 |
| Filing date | Oct 10, 2014 |
| Priority date | Oct 15, 2013 |
| Publication date | Aug 18, 2016 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
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.
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
containing two or more cycloaliphatic rings · CPC title
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
Related publications grouped by family.
Answers are generated from the same data shown on this page.