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US4131602A Expired / Lapsed US ⏱️ 0.0 years remaining

Radiation curable acrylated polyurethane

Assignee: Union Carbide Corp
•
Filing: 1977-09-29
•
Granted: 1978-12-26
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Expires: 1997-09-29
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Abstract

Abstract Radiation curable acrylated polyurethane is porduced by (a) producing an isocyanate-terminated intermediate by coreacting an organic diisocyanate with a combination of organic tri/tetraol and organic diol, said combination being chosen from polyester tri/tetraol-polyether diol and polyether tri/tetraol-polyester diol combinations; (b) reacting the isocyanate-terminated intermediate with an hydroxyacrylate such as 2-hydroxyethyl acrylate. Unexpectedly, the oligomer has desirably low viscosity, yet cures upon exposure to radiation to a coating having good physical properties.

Inventors

  • 👤 Leonard E. Hodakowski
  • 👤 Charles H. Carder

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 22:21
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/67; C08G18/671; C08G18/672; C08G18/40; C08G18/4009

Claims Analysis

Total Claims: 12
Claim 1
Independent Claim 195 words
An acrylated or methacrylated polyurethane produced by the process which comprises the steps of: (A) producing an isocyanate-terminated urethane intermediate by reacting (i) an organic diisocyanate; (ii) an organic tri/tetraol chosen from the group consisting of polyester tri/tetraols and polyether tri/tetraols; and (iii) an organic diol chosen from the group consisting of polyester diols and polyether diols, said organic diisocyanate being employed in equivalent excess to said organic tri/tetraol and organic diol; the ratio of organic diol to organic tri/tetraol employed being from about 1:1 to about 7:1; and provided that when the organic tri/tetraol is a polyester tri/tetraol the organic diol is a polyether diol, and when the organic tri/tetraol is a polyether tri/tetraol the organic diol is polyester diol; then (B) reacting the isocyanate-terminated urethane produced in step (A) with a sufficient amount of an hydroxyacrylate or hydroxymethacrylate to react at least 80% of the isocyanate groups of the intermediate, said hydroxyacrylate or hydroxymethacrylate having the formula ##STR5## wherein Z is hydrogen or methyl and X is linear or branched divalent alkylene of 1 to 10 carbon atoms, cycloalkylene of 5 to 12 carbon atoms, or arylene of 6 to 12 carbon atoms.
Claim 2
Dependent Claim 195 words
An acrylated or methacrylated polyurethane produced by the process which comprises the steps of: (A) producing an isocyanate-terminated urethane intermediate by reacting (i) an organic diisocyanate; (ii) an organic tri/tetraol chosen from the group consisting of polyester tri/tetraols and polyether tri/tetraols; and (iii) an organic diol chosen from the group consisting of polyester diols and polyether diols, said organic diisocyanate being employed in equivalent excess to said organic tri/tetraol and organic diol; the ratio of organic diol to organic tri/tetraol employed being from about 1:1 to about 7:1; and provided that when the organic tri/tetraol is a polyester tri/tetraol the organic diol is a polyether diol, and when the organic tri/tetraol is a polyether tri/tetraol the organic diol is polyester diol; then (B) reacting the isocyanate-terminated urethane produced in step (A) with a sufficient amount of an hydroxyacrylate or hydroxymethacrylate to react at least 80% of the isocyanate groups of the intermediate, said hydroxyacrylate or hydroxymethacrylate having the formula ##STR5## wherein Z is hydrogen or methyl and X is linear or branched divalent alkylene of 1 to 10 carbon atoms, cycloalkylene of 5 to 12 carbon atoms, or arylene of 6 to 12 carbon atoms.
Claim 3
Dependent Claim 26 words
An acrylated or methacrylated polyurethane as claimed in claim 1, wherein said polyether tri/tetraol and polyether diol have a molecular weight of from 300 to 4,000.
Claim 4
Dependent Claim 26 words
An acrylated or methacrylated polyurethane as claimed in claim 1, wherein said polyether tri/tetraol and polyether diol have a molecular weight of from 400 to 1,500.
Claim 5
Dependent Claim 26 words
An acrylated or methacrylated polyurethane as claimed in claim 1, wherein said polyester tri/tetraol and polyester diol have a molecular weight of from 300 to 4,000.
Claim 6
Dependent Claim 26 words
An acrylated or methacrylated polyurethane as claimed in claim 1, wherein the polyester tri/tetraol and polyester diol have a molecular weight of from 300 to 2,000.
Claim 7
Dependent Claim 44 words
An acrylated or methacrylated polyurethane as claimed in claim 1, wherein said organic tri/tetraol is a polyester tri/tetraol having a molecular weight of from 300 to 4,000 and said organic diol is a polyether diol having a molecular weight of from 300 to 4,000.
Claim 8
Dependent Claim 18 words
An acrylated or methacrylated polyurethane as claimed in claim 6, wherein said polyester tri/tetraol is a polylactone tri/tetraol.
Claim 9
Dependent Claim 17 words
An acrylated or methacrylated polyurethane as claimed in claim 7, wherein the polyether diol is polyoxypropylene diol.
Claim 10
Dependent Claim 25 words
An acrylated or methacrylated polyurethane as claimed in claim 1, wherein the mole ratio of organic diol to organic tri/tetraol is from 1:1 to 3:1.
Claim 11
Dependent Claim 33 words
An acrylated or methacrylated polyurethane as claimed in claim 1, wherein the equivalent ratio of organic diisocyanate to organic tri/tetraol and organic diol is at least greater than 1:1 up to about 2:1.
Claim 12
Dependent Claim 30 words
An acrylated or methacrylated polyurethane as claimed in claim 1, wherein the equivalent ratio of organic diisocyanate to organic tri/tetraol is at least greater than 1:1 up to about 1.3:1.

References Cited (Backward Citations)

US3891523A Cited
US3782961A Cited
US3642943A Cited
US3700643A Cited
US3741918A Cited
US3746665A Cited
US4013806A Cited
US3954584A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-12-25 1982-06-26 1982-12-26 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-12-25 1986-06-26 1986-12-26 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-12-25 1990-06-26 1990-12-26 $7700.00 Window Closed / Lapsed

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