Polyurethane-based protective coatings for rotor blades
US-2017306177-A1 · Oct 26, 2017 · US
US9732252B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9732252-B2 |
| Application number | US-201214400822-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 15, 2012 |
| Priority date | May 15, 2012 |
| Publication date | Aug 15, 2017 |
| Grant date | Aug 15, 2017 |
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Provided are reactive compositions for making a polyurethane-based rain-erosion protective coating for rotor blades, the reactive composition comprising an isocyanate-reactive component and an isocyanate-functional component and wherein the isocyanate-reactive component comprises a first component i) being a short chain hydroxyl-functional compound having two terminal (α-ω) hydroxyl groups, a molecular weight of less than 250 g/mole and containing at least 2 carbon atoms and a second component ii) comprising a high molecular weight hydroxyl-functional compound having two terminal (α-ω) hydroxyl groups and a molecular weight of at least 250 g/mol and comprising one or more units selected from oxyalkylene units and polyoxyalkylene units and wherein the isocyanate-functional component is an isocyanate prepolymer of the general formula NCO—Z—NCO, wherein Z is a linking group comprising at least two urethane (—NH—CO—O—) units and additionally one or more units selected from alkylenes, oxyalkylenes, polyoxyalkylenes, alkylene esters, oxyalkylene esters, polyoxyalkylene esters and combinations thereof. Also provided are protective coatings obtained from the reactive compositions and methods of applying the coatings to articles.
Opening claim text (preview).
The invention claimed is: 1. A reactive composition for making a polyurethane-based rain-erosion protective coating for rotor blades, the reactive composition comprising an isocyanate-reactive component and an isocyanate-functional component, wherein the isocyanate-reactive component comprises: a first component i) being a short chain hydroxyl-functional compound having two terminal (α-ω) hydroxyl groups, a molecular weight of less than 250 g/mole and containing at least 2 carbon atoms and a second component ii) comprising a high molecular weight hydroxyl-functional compound having two terminal (α-ω) hydroxyl groups and a molecular weight of at least 250 g/mol and comprising one or more units selected from oxyalkylene units and polyoxyalkylene units wherein the isocyanate-functional component is an isocyanate prepolymer of the general formula NCO—Z—NCO, wherein Z is a linking group comprising at least two urethane (—NH—CO—O—) units and additionally one or more units selected from alkylenes, oxyalkylenes, polyoxyalkylenes, alkylene esters, oxyalkylene esters, polyoxyalkylene esters and combinations thereof, wherein component ii) comprises a combination of α-ω dihydroxyl-functional compounds selected from oxyalkylene diols and polyoxyalkylene diols and said combination comprises a first fraction iia) of said diols having a molecular weight of from 250 g/mole up to about 600 g/mole and a second fraction iib) of said diols having a molecular weight of from about 800 g/mole up to about 5,000 g/mole and wherein the diols according to the first fraction iia) are present in an amount of from about one tenth to about one third of the amount of the diols according to the second fraction iib), wherein the amounts are based on weight, and wherein the diols according to the first component i) are present in an amount of from about one tenth to about one half of the amount of the diols according to the second fraction iib), wherein the amounts are based on weight, and wherein the reactive composition, when cured at 23° C. for 168 hours, has an elongation at break of at least 300%, a tensile strength of at least 20 MPa, and an irreversible deformation (permanent set) E from about 10% to about 50% after a first elongation/relaxation cycle with the cycle involving an elongation to 300%. 2. The reactive composition of claim 1 wherein the component i) is selected from alkane diols, alkane ether diols, alkane polyether diols, alkane ester diols containing from about 3 to 12 carbon atoms. 3. The reactive composition of claim 1 wherein the high molecular weight hydroxyl-functional compound comprises dihydroxyl-functional compounds selected from oxyalkylene diols and polyoxyalkylene diols having two terminal (α-ω) hydroxyl groups, a molecular weight of from at least about 250 g/mole up to about 10,000 g/mole. 4. The reactive composition of claim 1 having a viscosity at room temperature (23° C.) of from about 1000 to about 5000 mPas (DIN EN ISO 2884). 5. A rain-erosion protective coating on the external surface of a rotor blade, wherein the coating comprises the reaction product of a reactive composition comprising an isocyanate-reactive component and an isocyanate-functional component and wherein the isocyanate-reactive component comprises a first component i) being a short chain hydroxyl-functional compound having two terminal (α-ω) hydroxyl groups having a molecular weight of less than 250 g/mole and having at least 2 carbon atoms, and a second component ii) comprising a high molecular weight hydroxyl-functional compound having two terminal (α-ω hydroxyl groups and a molecular weight of at least 250 g/mol and comprising one or more units selected from oxyalkylene units and polyoxyalkylene units, wherein the isocyanate-functional component is an isocyanate prepolymer of the general formula NCO—Z—NCO, wherein Z is a linking group comprising at least two urethane (—NH—CO—O—) units and additionally one or more units selected from alkylenes, oxyalkylenes, polyoxyalkylenes, alkylene esters, oxyalkylene esters, polyoxyalkylene esters and combinations thereof, wherein component ii) comprises a combination of α-ω dihydroxyl-functional compounds selected from oxyalkylene diols and polyoxyalkylene diols and said combination comprises a first fraction iia) of said diols having a molecular weight of from 250 g/mole up to about 600 g/mole and a second fraction iib) of said diols having a molecular weight of from about 800 g/mole up to about 5,000 g/mole and wherein the diols according to the first fraction iia) are present in an amount of from about one tenth to about one third of the amount of the diols according to the second fraction iib), wherein the amounts are based on weight, and wherein the diols according to the first component are present in an amount of from about one tenth to about one half of the amount of the diols according to the second fraction iib), wherein the amounts are based on weight, and wherein the coating has an elongation at break of at least 300%, a tensile strength of at least 20 MPa, and an irreversible deformation (permanent set) E from about 10% to about 50% after a first elongation/relaxation cycle with the cycle involving an elongation to 300%. 6. The protective coating according to claim 5 wherein the component i) is selected from alkane diols, alkane ether diols, alkane polyether diols, alkane ester diols containing from about 3 to 12 carbon atoms. 7. The protective coating according to claim 5 wherein the high molecular weight hydroxyl-functional compound comprises dihydroxyl-functional compounds selected from oxyalkylene diols and polyoxyalkylene diols having two terminal (α-ω) hydroxyl groups, a molecular weight of from at least about 250 g/mole up to about 10,000 g/mole. 8. The protective coating of claim 5 wherein the article is a rotor blade wherein the leading edge of the rotor blade has a length of at least about 30 m. 9. The protective coating of claim 5 wherein the protective coating is the outermost layer of at least a part of the external surface of the rotor blade.
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