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US3719638A Expired / Lapsed US ⏱️ 0.0 years remaining

Radiation curable acrylic urethane monomers

Assignee: Individual
•
Filing: 1969-10-29
•
Granted: 1973-03-06
•
Expires: 1989-10-29
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Abstract

Abstract A radiation curable composition is provided by reacting about one mole of an organic diisocyanate with about one mole of a hydroxyacrylate to form a mono-urethane adduct which is subsequently reacted with a styrene-allyl alcohol copolymer having a molecular weight between about 200 and 30,000, the reaction product being essentially free of unreacted isocyanate groups.

Inventors

  • 👤 T Huemmer
  • 👤 T Miranda

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 21:24
CPC Classifications
G; G03; G03F; G03F7/00; G03F7/004; G03F7/038; C; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/40; C08G18/62; C08G18/6212; C08G18/70; C08G18/72; C08G18/80; C08G18/8061; C08G18/8064; C08G18/81; C08G18/8141; C08G18/815; C08G18/8158

Claims Analysis

Total Claims: 14
Claim 1
Independent Claim 85 words
An acrylic urethane reaction product which is stable at room temperature and curable by electron beam radiation to yield a solvent-resistant solid polymer comprising the reaction product of one hydroxy equivalent of a styrene-allyl alcohol copolymer having a molecular weight of from about 200 to about 30,000 and up to one mole of a mono-urethane adduct formed by reacting at least one mole of a hydroxy acrylate, and about one mole of an organic diisocyanate, said reaction product being essentially free of unreacted isocyanate groups.
Claim 2
Dependent Claim 85 words
An acrylic urethane reaction product which is stable at room temperature and curable by electron beam radiation to yield a solvent-resistant solid polymer comprising the reaction product of one hydroxy equivalent of a styrene-allyl alcohol copolymer having a molecular weight of from about 200 to about 30,000 and up to one mole of a mono-urethane adduct formed by reacting at least one mole of a hydroxy acrylate, and about one mole of an organic diisocyanate, said reaction product being essentially free of unreacted isocyanate groups.
Claim 3
Dependent Claim 16 words
A reaction product in accordance with claim 1, in which the diisocyanate is an aromatic diisocyanate.
Claim 4
Dependent Claim 14 words
A reaction product in accordance with claim 2, wherein the diisocyanate is toluene diisocyanate.
Claim 5
Dependent Claim 39 words
A reaction product in accordance with claim 1, wherein the hydroxy acrylate is selected from the group consisting of hydroxyalkyl acrylates and hydroxyalkyl methacrylates, wherein the alkyl group contains at least two, but not more than six carbon atoms.
Claim 6
Dependent Claim 16 words
A reaction product in accordance with claim 4, wherein the hydroxyacrylate contains a primary hydroxyl group.
Claim 7
Dependent Claim 31 words
A reaction product in accordance with claim 1, wherein the isocyanate contains intermediate urethane groups, and is the isocyanate terminated reaction product of a diisocyanate and a hydroxy containing organic compound.
Claim 8
Dependent Claim 19 words
A reaction product in accordance with claim 1, wherein said copolymer contains at least 3 hydroxy groups per molecule.
Claim 9
Dependent Claim 33 words
A reaction product in accordance with claim 1, formed by the reaction of about 1 mole of hydroxyethyl acrylate, one mole of toluene diisocyanate and one hydroxy equivalent of saiD styrene-allyl alcohol copolymer.
Claim 10
Independent Claim 86 words
A method of preparing an acrylic urethane reaction product which is stable at room temperature and curable by electron beam radiation to yield a solvent-resistant solid polymer, comprising as a first step reacting approximately equimolar quantities of a hydroxy acrylate and an organic diisocyanate, and a second step, reacting the product of the first step with a styrene-allyl alcohol copolymer having a molecular weight of from about 200 to about 30,000, the quantity of said copolymer being sufficient to react with essentially all free isocyanate groups.
Claim 11
Independent Claim 86 words
A method of preparing an acrylic urethane reaction product which is stable at room temperature and curable by electron beam radiation to yield a solvent-resistant solid polymer, comprising as a first step reacting approximately equimolar quantities of a hydroxy acrylate and an organic diisocyanate, and a second step, reacting the product of the first step with a styrene-allyl alcohol copolymer having a molecular weight of from about 200 to about 30,000, the quantity of said copolymer being sufficient to react with essentially all free isocyanate groups.
Claim 12
Dependent Claim 18 words
A method as described in claim 9, wherein the second step is carried out in a polymerizable solvent.
Claim 13
Dependent Claim 38 words
A method as described in claim 9, wherein said hydroxy acrylate is selected from the group consisting of hydroxyalkyl acrylates and hydroxyalkyl methacrylates, wherein the alkyl group contains at least two, but no more than six carbon atoms.
Claim 14
Dependent Claim 14 words
A method as described in claim 11, wherein said hydroxy acrylate is hydroxyethyl acrylate.

References Cited (Backward Citations)

No citation records indexed.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1976-03-05 1976-09-04 1977-03-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1980-03-05 1980-09-04 1981-03-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1984-03-05 1984-09-04 1985-03-06 $7700.00 Window Closed / Lapsed

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