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US4163094A Expired / Lapsed US ⏱️ 0.0 years remaining

Heat curing water soluble homopolyurethanes

Assignee: Lilly Industries Inc
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Filing: 1978-04-07
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Granted: 1979-07-31
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Expires: 1998-04-07
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Abstract

Abstract A one-step process for synthesizing water soluble self-curing polyurethanes is achieved by co-reacting certain monomers under controlled conditions to form a blocked, water soluble polyurethane which can be subsequently dispersed in water. The polyurethane polymer is substantially free of high molecular weight hydrocarbon chains and essentially comprises all polyurethane units and is adapted to self-cross link upon being subjected to heat. The polymer is particularly suitable for producing polyurethane protective coatings which exhibit substantially increased film hardness, abrasion resistance, as well as other desirable film integrity properties.

Inventors

  • 👤 Edward T. Turpin

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-27 22:00
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/30; C08G18/34; C08G18/348; C08G18/08; C08G18/0804; C08G18/0819; C08G18/0823; C08G18/70; C08G18/72; C08G18/80; C08G18/8061

Claims Analysis

Total Claims: 3
Claim 1
Independent Claim 319 words
In a process for manufacturing a water soluble homopolymer polyurethane being self-curing upon application of heat, comprising the steps of: copolymerizing on a weight basis (a) 16% to 87% of a partially blocked polyisocyanate containing on an average between 0.05 and 2 equivalents blocked isocyanate groups and between 1 and 2 equivalents of reactive isocyanate groups per molecule of polyisocyanate, (b) 5% to 84% of a low molecular weight dihydroxy-acid containing at least one non-reactive group and at least two reactive hydroxyls and of the general structure ##STR2## wherein R is a hydrogen, a hydroxymethyl, or an alkyl having up to 20 carbon atoms, and the hydroxyl groups being reactive to copolymerize with the reactive isocyanate groups on said polyisocyanate to provide repeating urethane linkages, and (c) 0% to 69% of a polyol selected from diols and triols, having a molecular weight less than 500, said polyols having at least two reactive hydroxyls for copolymerizing with the reactive isocyanate groups on said polyisocyanate to provide repeating urethane linkages, said dihydroxy-acid (b) and said polyol (c) collectively containing at least about 2.5% excess equivalents of reactive hydroxyls relative equivalents of reactive isocyanate groups on said polyisocyanate (a) to completely react available reactive isocyanate groups into urethane linkages, said polyisocyanate (a) and said dihydroxy-acid (b) and said polyol (c) being copolymerized at temperatures between about 50° C. and 100° C. to form a homopolymer polyurethane containing repeating urethane linkages and having blocked isocyanate groups, unreacted hydroxyl groups and unreacted carboxyl groups; neutralizing the unreacted carboxyl groups on said homopolymer polyurethane with a base and solubilizing said homopolymer polyurethane in water to provide a stabilized aqueous polyurethane mixture; coating a substrate with a film of said aqueous polyurethane mixture; and heating the film at temperatures above about 150° C. for time sufficient to heat cure the film by cross-linking the blocked isocyanate groups with the unreacted hydroxyl groups of said homopolymer polyurethane.
Claim 2
Dependent Claim 319 words
In a process for manufacturing a water soluble homopolymer polyurethane being self-curing upon application of heat, comprising the steps of: copolymerizing on a weight basis (a) 16% to 87% of a partially blocked polyisocyanate containing on an average between 0.05 and 2 equivalents blocked isocyanate groups and between 1 and 2 equivalents of reactive isocyanate groups per molecule of polyisocyanate, (b) 5% to 84% of a low molecular weight dihydroxy-acid containing at least one non-reactive group and at least two reactive hydroxyls and of the general structure ##STR2## wherein R is a hydrogen, a hydroxymethyl, or an alkyl having up to 20 carbon atoms, and the hydroxyl groups being reactive to copolymerize with the reactive isocyanate groups on said polyisocyanate to provide repeating urethane linkages, and (c) 0% to 69% of a polyol selected from diols and triols, having a molecular weight less than 500, said polyols having at least two reactive hydroxyls for copolymerizing with the reactive isocyanate groups on said polyisocyanate to provide repeating urethane linkages, said dihydroxy-acid (b) and said polyol (c) collectively containing at least about 2.5% excess equivalents of reactive hydroxyls relative equivalents of reactive isocyanate groups on said polyisocyanate (a) to completely react available reactive isocyanate groups into urethane linkages, said polyisocyanate (a) and said dihydroxy-acid (b) and said polyol (c) being copolymerized at temperatures between about 50° C. and 100° C. to form a homopolymer polyurethane containing repeating urethane linkages and having blocked isocyanate groups, unreacted hydroxyl groups and unreacted carboxyl groups; neutralizing the unreacted carboxyl groups on said homopolymer polyurethane with a base and solubilizing said homopolymer polyurethane in water to provide a stabilized aqueous polyurethane mixture; coating a substrate with a film of said aqueous polyurethane mixture; and heating the film at temperatures above about 150° C. for time sufficient to heat cure the film by cross-linking the blocked isocyanate groups with the unreacted hydroxyl groups of said homopolymer polyurethane.
Claim 3
Dependent Claim 21 words
The process in claim 1 wherein said homopolymer polyurethane is neutralized with a base selected from ammonia or an organic amine.

References Cited (Backward Citations)

US3773729A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-07-30 1983-01-29 1983-07-31 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-07-30 1987-01-29 1987-07-31 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-07-30 1991-01-29 1991-07-31 $7700.00 Window Closed / Lapsed

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