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US4119602A Expired / Lapsed US ⏱️ 0.0 years remaining

Aqueous urethane codispersions

Assignee: WR Grace and Co
•
Filing: 1977-04-07
•
Granted: 1978-10-10
•
Expires: 1997-04-07
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Abstract

Abstract Disclosed herein are aqueous dispersions of blocked hydrophilic polyether urethane prepolymers and codispersions thereof with synthetic polymer latices. Also disclosed are methods of preparing the dispersions as well as polyurethane coatings and films prepared therewith. The dispersion/codispersions are characterized by good mechanical stability and resistance to freeze - thaw cycles. Coatings, films and impregnated articles prepared therefrom possess good physical properties. Coatings and films prepared from codispersions containing acrylic latex possess physical properties, chemical solvent resistance, etc. comparable to solvent-based urethanes.

Inventors

  • 👤 Irving E. Isgur
  • 👤 Robert R. Alexander
  • 👤 Thomas P. Moy

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 12:41
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/08; C08G18/10; C08G18/28; C08G18/40; C08G18/48; C08G18/4833; C08L; C08L75/00; C08L75/04; C08L75/08

Claims Analysis

Total Claims: 24
Claim 1
Independent Claim 231 words
An anionically stabilized aqueous codispersion of a blocked urethane prepolymer and a synthetic polymer latex, said codispersion having a solids loading not exceeding about 50%, said blocked prepolymer comprising the condensation product of a hydrophilic polyoxyalkylene urethane prepolymer with an oxime and having a decomposition temperature of from about 140° to about 180° C.; said synthetic polymer latex having a pH value of at least about 6 selected from the group consisting of (1) copolymeric latex of a vinyl carboxylic acid with at least one additional ethylenically polymerizable monomer selected from the group consisting of (a) vinyl aromatic hydrocarbons (b) vinyl aliphatic hydrocarbons, (c) derivatives of acrylic acid, and (d) vinyl chloride, (2) butadiene-acrylonitrile latex, (3) polystyrene latex, (4) vinylpyridine latex, (5) styrene-butadiene latex, and (6) acrylic latex, said urethane prepolymer being water-dispersible and the reaction product of a polyoxyalkylene polyol containing at least 50 mole percent ethylene oxide, a molecular weight between about 200 to 20,000 and a hydroxy functionality of from about 2 to 8 with an excess of a polyisocyanate; said blocked prepolymer having a NOH/NCO molar ratio of from about 0.65 to about 1.1, said blocked prepolymer being from about 5 to about 95% of the solids content of said codispersion with the balance of the solids being said synthetic polymer latex; said codispersion having a pH value adjusted to a value of at least about 9.
Claim 2
Dependent Claim 231 words
An anionically stabilized aqueous codispersion of a blocked urethane prepolymer and a synthetic polymer latex, said codispersion having a solids loading not exceeding about 50%, said blocked prepolymer comprising the condensation product of a hydrophilic polyoxyalkylene urethane prepolymer with an oxime and having a decomposition temperature of from about 140° to about 180° C.; said synthetic polymer latex having a pH value of at least about 6 selected from the group consisting of (1) copolymeric latex of a vinyl carboxylic acid with at least one additional ethylenically polymerizable monomer selected from the group consisting of (a) vinyl aromatic hydrocarbons (b) vinyl aliphatic hydrocarbons, (c) derivatives of acrylic acid, and (d) vinyl chloride, (2) butadiene-acrylonitrile latex, (3) polystyrene latex, (4) vinylpyridine latex, (5) styrene-butadiene latex, and (6) acrylic latex, said urethane prepolymer being water-dispersible and the reaction product of a polyoxyalkylene polyol containing at least 50 mole percent ethylene oxide, a molecular weight between about 200 to 20,000 and a hydroxy functionality of from about 2 to 8 with an excess of a polyisocyanate; said blocked prepolymer having a NOH/NCO molar ratio of from about 0.65 to about 1.1, said blocked prepolymer being from about 5 to about 95% of the solids content of said codispersion with the balance of the solids being said synthetic polymer latex; said codispersion having a pH value adjusted to a value of at least about 9.
Claim 3
Dependent Claim 12 words
A codispersion as in claim 1 wherein the oxime is butanone oxime.
Claim 4
Dependent Claim 12 words
A codispersion as in claim 1 wherein the oxime is acetone oxime.
Claim 5
Dependent Claim 12 words
A codispersion as in claim 1 wherein the oxime is cyclohexanone oxime.
Claim 6
Dependent Claim 26 words
A codispersion as in claim 1 wherein the synthetic polymer latex is stable at a pH of from 9.5 to 11 for at least 1/2 hour.
Claim 7
Dependent Claim 20 words
A codispersion as in claim 1 wherein at least 50% by weight of the solids content is the blocked prepolymer.
Claim 8
Dependent Claim 11 words
A codispersion as in claim 1 wherein the latex is styrene-butadiene.
Claim 9
Dependent Claim 13 words
A codispersion as in claim 1 wherein the latex is an acrylic latex.
Claim 10
Dependent Claim 28 words
An aqueous codispersion as in claim 1 wherein the polyol component of the prepolymer is polyoxyethylene glycol admixed with a monomeric alcohol having three hydroxyl groups per mole.
Claim 11
Dependent Claim 14 words
A codispersion as in claim 9 wherein the monomeric alcohol is trimethylolpropane or trimethylolethane.
Claim 12
Dependent Claim 116 words
The anionically stabilized aqueous codispersion of claim 1 wherein the polyoxyalkylene polyol is selected from (1) essentially linear polyols formed by the reaction of ethylene oxide with an initiator, (2) linear random or block copolymer polyols formed by the reaction of mixtures of ethylene oxide and propylene oxide with an initiator, (3) branched polyols with a hydroxy functionality of at least three formed by reacting alkylene oxides selected from ethylene oxide, propylene oxides and mixtures thereof with a polyfunctional initiator selected from the group consisting of trimethylolpropane, and pentaaerythritol and (4) linear branched polyfunctional polyols formed by the reaction of mixed linear and branched initiators with ethylene oxide or mixtures of ethylene oxide and propylene oxide.
Claim 13
Independent Claim 234 words
A method for preparing an anionically stabilized aqueous codispersion of a blocked urethane prepolymer and a synthetic polymer latex comprising (1) admixing (a) an aqueous dispersion of cationically stabilized hydrophilic polyoxyalkylene urethane prepolymer wherein the isocyanate groups are blocked by formation of a condensation product with an oxime, said block prepolymer being water-dispersible and having a decomposition temperature of from about 140° to 180° C. and (b) an aqueous synthetic polymer latex having a pH of at least 6, and (2) adjusting the pH of the resulting codispersion to at least 9; wherein said synthetic polymer latex is selected from the group consisting of (1) copolymeric latex of a vinyl carboxylic acid with at least one additional ethylenically polymerizable monomer selected from the group consisting of (a) vinyl aromatic hydrocarbons, (b) vinyl aliphatic hydrocarbons, (c) derivatives of acrylic acid, and (d) vinyl chloride, (2) butadiene-acrylonitrile latex, (3) polystyrene latex, (4) vinylpyridine latex, (5) styrene-butadiene latex, and (6) acrylic latex; said blocked prepolymer being the reaction product of a polyoxyalkylene polyol containing at least 50 mole percent ethylene oxide, a molecular weight between about 200 and 20,000 and a hydroxy functionality of from about 2 to 8 with an excess of a polyisocyanate; said blocked prepolymer having a NOH/NCO molar ratio of from about 0.65 to about 1.1; said blocked prepolymer being from about 5 to about 95% of the solids content of said codispersion.
Claim 14
Independent Claim 234 words
A method for preparing an anionically stabilized aqueous codispersion of a blocked urethane prepolymer and a synthetic polymer latex comprising (1) admixing (a) an aqueous dispersion of cationically stabilized hydrophilic polyoxyalkylene urethane prepolymer wherein the isocyanate groups are blocked by formation of a condensation product with an oxime, said block prepolymer being water-dispersible and having a decomposition temperature of from about 140° to 180° C. and (b) an aqueous synthetic polymer latex having a pH of at least 6, and (2) adjusting the pH of the resulting codispersion to at least 9; wherein said synthetic polymer latex is selected from the group consisting of (1) copolymeric latex of a vinyl carboxylic acid with at least one additional ethylenically polymerizable monomer selected from the group consisting of (a) vinyl aromatic hydrocarbons, (b) vinyl aliphatic hydrocarbons, (c) derivatives of acrylic acid, and (d) vinyl chloride, (2) butadiene-acrylonitrile latex, (3) polystyrene latex, (4) vinylpyridine latex, (5) styrene-butadiene latex, and (6) acrylic latex; said blocked prepolymer being the reaction product of a polyoxyalkylene polyol containing at least 50 mole percent ethylene oxide, a molecular weight between about 200 and 20,000 and a hydroxy functionality of from about 2 to 8 with an excess of a polyisocyanate; said blocked prepolymer having a NOH/NCO molar ratio of from about 0.65 to about 1.1; said blocked prepolymer being from about 5 to about 95% of the solids content of said codispersion.
Claim 15
Dependent Claim 12 words
A method as in claim 12 wherein the oxime is butanone oxime.
Claim 16
Dependent Claim 12 words
A method as in claim 12 wherein the oxime is acetone oxime.
Claim 17
Dependent Claim 12 words
A method as in claim 12 wherein the oxime is cyclohexanone oxime.
Claim 18
Dependent Claim 26 words
A method as in claim 12 wherein the synthetic polymer latex is stable at a pH of from 9.5 to 11 for at least 1/2 hour.
Claim 19
Dependent Claim 20 words
A method as in claim 12 wherein at least 50% by weight of the solids content is the blocked prepolymer.
Claim 20
Dependent Claim 11 words
A method as in claim 12 wherein the latex is styrene-butadiene.
Claim 21
Dependent Claim 13 words
A method as in claim 12 wherein the latex is an acrylic latex.
Claim 22
Dependent Claim 27 words
A method as in claim 12 wherein the polyol component of the prepolymer is polyoxyethylene glycol admixed with a monomeric alcohol having three hydroxyl groups per mole.
Claim 23
Dependent Claim 14 words
A method as in claim 20 wherein the monomeric alcohol is trimethylolpropane or trimethylolethane.
Claim 24
Dependent Claim 116 words
A method as in claim 12 wherein the polyoxyalkylene polyol is selected from the group consisting of (1) essentially linear polyols formed by the reaction of ethylene oxide with an initiator, (2) linear random or block copolymer polyols formed by the reaction of mixtures of ethylene oxide and propylene oxide with an initiator, (3) branched polyols with a hydroxy functionality of at least three formed by reacting alkylene oxides selected from the group consisting of ethylene oxide, and propylene oxides with a polyfunctional initiator selected from trimethylolpropane, and pentaerythritol, and (4) linear branched polyfunctional polyols formed by the reaction of mixed linear and branched initiators with ethylene oxide or mixtures of ethylene oxide and propylene oxide.

References Cited (Backward Citations)

CA671042A Cited
US3898197A Cited
US3903232A Cited
US4039517A Cited
US3998768A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-10-09 1982-04-10 1982-10-10 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-10-09 1986-04-10 1986-10-10 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-10-09 1990-04-10 1990-10-10 $7700.00 Window Closed / Lapsed

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