US4618635A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Coating compositions prepared from lactone-acrylate adduct, polyol and isocyanate
Assignee: Union Carbide Corp
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Filing: 1985-05-17
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Granted: 1986-10-21
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Expires: 2005-05-17
Abstract
Abstract Described herein are compositions comprising the reaction product of a polyol, a multi-functional isocyanate, a lactone-acrylate adduct and an hydroxyalkyl acrylate. These compositions are suitable for use as curable coatings.
Inventors
- 👤 Claiborn L. Osborn
- 👤 Joseph V. Koleske
- 👤 Kenneth Drake
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-04 14:22
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/67; C08G18/671; C08G18/672; C08G18/6725
Claims Analysis
Total Claims: 31
Claim 1
Independent Claim
25 words
A composition suitable for use as a radiation curable coating comprising the reaction product of a polycaprolactone polyol, a multi-functional isocyanate, and a lactone-acrylate adduct.
Claim 2
Dependent Claim
25 words
A composition suitable for use as a radiation curable coating comprising the reaction product of a polycaprolactone polyol, a multi-functional isocyanate, and a lactone-acrylate adduct.
Claim 3
Dependent Claim
15 words
A composition as defined in claim 1 wherein the reaction product contains an hydroxyalkyl acrylate.
Claim 4
Dependent Claim
72 words
A composition as defined in claim 1 wherein the multi-functional isocyanate is selected from 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, isophorone diisocyanate, 4,4'-diphenylmethane diisocyanate, di(2-isocyanathoethyl)-bicyclo (2.2.1) hept-5-ene-2,3-dicarboxylate, 3,5,5-tri-ethyl-1-isocyanato-3-isocynato-methylcyclohexane, 1,6-hexamethylene diisocyanate, m-and p-xylene diisocyanate, cyclohexane-1,4-diisocyanate, 4,4'-dicyclohexyl methane diisocyanate, tetramethylene diisocyanate, cyclopentylene-1,3- diisocyanate, 1,3-diisocyanate, 1,4-xylene diisocyanate, 1,5-naphthalene diisocyanate, m-phenylene diisocyanate, p-phenylene diisocyanate, hexamethylene diisocyanate, 3,3'-dimethyl -4,4'-diphenylmethane diisocyanate, 4,4'-diphenylene diisocyanate, 3,3'-dimethoxy-4,4'-dimethyl-4,4'-biphenylene diisocyanate, durene diisocyanate, 1-phenoxy-2,4-phenylene diisocyanate, 1-tert-butyl-2,4-phenylene diisocyanate, 2,2,4-trimethylhexamethylene diisocyanate, 1,3,5-benzene triisocyanate, 2,4,6-toluene triisocyanate, or mixtures thereof.
Claim 5
Dependent Claim
21 words
A composition as defined in claim 1 wherein the lactone-acrylate adduct is prepared by reacting a lactone with an hydroxyalkyl acrylate.
Claim 6
Dependent Claim
39 words
A composition as defined in claim 4 wherein the lactone is characterized by the following formula: ##STR7## wherein the R''s are independently hydrogen or alkyl of from 1 to 12 carbon atoms, and x is from 4 to 7.
Claim 7
Dependent Claim
12 words
A composition as defined in claim 5 wherein the lactone is epsilon-carprolactone.
Claim 8
Dependent Claim
27 words
A composition as defined in claim 4 wherein the hydroxyalkyl acrylate is selected from 2-hydroxyethyl acrylate, hydroxypropyl acrylate, hydroxybutyl acrylate, 2-hydroxy-3-chloropropylacrylate, 2,3-dihydroxy propyl acrylate, or mixtures thereof.
Claim 9
Dependent Claim
14 words
A composition as defined in claim 7 wherein the hydroxyalkyl acrylate is hydroxyethyl acrylate.
Claim 10
Dependent Claim
17 words
A composition as defined in claim 2 wherein the hydroxyalkyl acrylate is as defined in claim 7.
Claim 11
Dependent Claim
12 words
A composition as defined in claim 1 which contains a reactive solvent.
Claim 12
Dependent Claim
59 words
A composition as defined in claim 10 wherein the reactive solvent is of the following formula: ##STR8## wherein X is hydrogen or methyl and R 2 can be substituted or unsubstituted alkyl, cycloalkyl, alkenyl, aryl, or aralkyl, wherein the substituent can be alkoxy, hydroxy, cyano, or amino, or R 2 can be carbamoyloxy alkyl which can be N-alkyl substituted.
Claim 13
Dependent Claim
16 words
A composition as defined in claim 10 wherein the reactive solvent is a multi-functional alkyl acrylate.
Claim 14
Dependent Claim
35 words
A composition as defined in claim 12 wherein the reactive solvent is 1,6-hexanediol diacrylate, neopentyl glycol diacrylate, tetramethyleneglycol diacrylate, esterdiol-204-diacrylate, trimethylolpropane triacylate, triethyleneglycol diacrylate, the diacrylate of an alkoxylated esterdiol 204, or mixtures thereof. PG,52
Claim 15
Dependent Claim
13 words
A composition as defined in claim 10 wherein the reactive solvent is N-vinylpyrrolidone.
Claim 16
Dependent Claim
20 words
A composition as defined in claim 12 wherein the reactive solvent is a lactone-acrylate adduct reacted with a multi-functional isocyanate.
Claim 17
Dependent Claim
12 words
A composition as defined in claim 1 which contains a non-reactive solvent.
Claim 18
Dependent Claim
26 words
A composition as defined in claim 16 wherein the solvent is cyclohexanone, toluene, methyl isobutyl ketone, tetrahydrofuran, methyl amyl ketone, ethoxy ethyl acetate, and mixtures thereof.
Claim 19
Dependent Claim
14 words
A cured coating prepared from the composition of claim 1 or 10 or 16.
Claim 20
Dependent Claim
52 words
A composition suitable for use as a radiation curable coating comprising the reaction product of (a) a polycaprolactone polyol; (b) a multifunctional isocyanate; and (c) a lactone-acrylate adduct wherein in excess of 20 percent by weight of component (a), based on the total weight of components (a), (b) and (c), is reacted.
Claim 21
Dependent Claim
52 words
A composition suitable for use as a radiation curable coating comprising the reaction product of (a) a polycaprolactone polyol; (b) a multifunctional isocyanate; and (c) a lactone-acrylate adduct wherein in excess of 20 percent by weight of component (a), based on the total weight of components (a), (b) and (c), is reacted.
Claim 22
Dependent Claim
57 words
A composition suitable for use as a radiation curable coating comprising the reaction product of (a) a polycaprolactone polyol; (b) a multifunctional isocyanate; (c) a lactone-acrylate adduct; and (d) an hydroxyalkyl acrylate wherein in excess of 20 percent by weight of component (a), based on the total weight of components (a), (b), (c) and (d) is reacted.
Claim 23
Dependent Claim
57 words
A composition suitable for use as a radiation curable coating comprising the reaction product of (a) a polycaprolactone polyol; (b) a multifunctional isocyanate; (c) a lactone-acrylate adduct; and (d) an hydroxyalkyl acrylate wherein in excess of 20 percent by weight of component (a), based on the total weight of components (a), (b), (c) and (d) is reacted.
Claim 24
Dependent Claim
12 words
A composition as defined in claim 20 which contains a reactive solvent.
Claim 25
Dependent Claim
12 words
A composition as defined in claim 20 which contains a non-reactive solvent.
Claim 26
Dependent Claim
12 words
A composition as defined in claim 19 which contains a reactive solvent.
Claim 27
Dependent Claim
12 words
A composition as defined in claim 19 which contains a non-reactive solvent.
Claim 28
Dependent Claim
26 words
A composition as defined in claim 1 wherein said isocyanate is reacted with said polyol, followed by the reaction of that product with said lactone-acrylate adduct.
Claim 29
Dependent Claim
30 words
A composition as defined in claim 2 wherein said isocyanate is reacted with said polyol, followed by the reaction of that product with the lactone-acrylate adduct and said hydroxylalkyl acrylate.
Claim 30
Dependent Claim
26 words
A composition as defined in claim 19 wherein said isocyanate is reacted with said polyol, followed by the reaction of that product with said lactone-acrylate adduct.
Claim 31
Dependent Claim
26 words
A composition as defined in claim 20 wherein said isocynate is reacted with said polyol, followed by the reaction of that product with said lactone-acrylate adduct.
References Cited (Backward Citations)
US3700643A
Cited
US4188472A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
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| 3.5 Years (Year 4) | 1989-10-20 | 1990-04-21 | 1990-10-21 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1993-10-20 | 1994-04-21 | 1994-10-21 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1997-10-20 | 1998-04-21 | 1998-10-21 | $7700.00 | Window Closed / Lapsed |