Patent US4786586A successfully refreshed from Google Patents.
US4786586A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Radiation curable coating for photographic laminate
Assignee: ATK Launch Systems LLC
•
Filing: 1987-02-12
•
Granted: 1988-11-22
•
Expires: 2007-02-12
Abstract
Abstract Compositions comprising an impermeable acrylate-terminated oligomer, at least one reactive diluent, and alpha-hydroxycyclohexylphenyl ketone, diethoxyacetophenone, 1-(4-dodecylphenyl)-2-hydroxy-2-methylpropan-1-one, or 2-hydroxy-2-methyl-1-phenylpropan-1-one as a photoinitiator, are disclosed. These compositions have utility in optical coatings.
Inventors
- 👤 San A. Lee
- 👤 Stuart M. Ellerstein
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-31 17:52
CPC Classifications
G; G03; G03F; G03F7/00; G03F7/004; G03F7/027; C; C08; C08F; C08F290/00; C08F290/02; C08F290/06; C08F290/064; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/40; C08G18/62; C08G18/6204; C08G18/6208; C08G18/67; C08G18/671; C08G18/672; G03C; G03C1/00; G03C1/76; G03C1/7614; G03C9/00; Y; Y10; Y10S; Y10S430/00; Y10S430/162
Claims Analysis
Total Claims: 6
Claim 1
Independent Claim
392 words
Unexposed photographic color print material comprising a laminate of a photoemulsion layer having front and back sides and an optically clear coating layer having front and back sides, wherein: A. said photoemulsion layer is adapted to be exposed to the image of a color print negative projected through said coating layer, developed by an immersion development process, and viewed through said coating layer following said development process; B. the front side of said coating layer is the front outside surface of said color print material, and is adapted to be in contact with immersion development process chemicals during develpment of said print material; C. the back side of said coating layer faces the front side of said photoemulsion layer; D. said coating layer has the property of being essentially non-yellowing during and after immersion of said color print material in immersion development process chemicals with said coating layer in direct contact with said chemicals; and E. said coating layer consists essentially of the cured reaction product of: (i) from 45 to 80 percent, based upon total weight of the composition, of an oligomer of the formula: ##STR5## where R 1 is a linear or branched hydrocarbon polymer of from 1,000 to 4,000 molecular weight selected from the group consisting of fully hydrogenated 1,2-polybutadiene; 1,2-polybutadiene hydrogenated to an iodine number of from 9 to 21; and fully hydrogenated polyisobutylene; R 2 is a linear, branched or cyclic alkylene of from six to twenty carbon atoms; and X and Q are independently either (a) a radical of the formula: ##STR6## wherein R 3 , R 4 , and R 5 are independently hydrogen or methyl, m is an integer from 1 to 10, and p is either zero or one, or (b) a saturated alkyl radical of from nine to twenty carbon atoms, with the proviso that said oligomer must possess at least one acrylate or methacrylate terminal group; (ii) from 20 to 50 percent, based on total weight of the composition, of an acrylate or methacrylate terminated reactive diluent of from 11 to 22 carbon atoms; and (iii) from 0.5 to 5 percent, based upon the total weight of the composition, of a photoinitiator selected from the goup consisting of alpha-hydroxycyclohexylphenyl ketone, diethoxyacetophenone, 1-(4-dodecylphenyl)-2-hydroxy-2-methyl-propan-1-one, 2-hydroxy-2-methyl-1-phenyl-propan-1-one, and mixtures thereof; wherein R 1 and R 2 are free of aromatic, ether, or ester functional groups.
Claim 2
Dependent Claim
392 words
Unexposed photographic color print material comprising a laminate of a photoemulsion layer having front and back sides and an optically clear coating layer having front and back sides, wherein: A. said photoemulsion layer is adapted to be exposed to the image of a color print negative projected through said coating layer, developed by an immersion development process, and viewed through said coating layer following said development process; B. the front side of said coating layer is the front outside surface of said color print material, and is adapted to be in contact with immersion development process chemicals during develpment of said print material; C. the back side of said coating layer faces the front side of said photoemulsion layer; D. said coating layer has the property of being essentially non-yellowing during and after immersion of said color print material in immersion development process chemicals with said coating layer in direct contact with said chemicals; and E. said coating layer consists essentially of the cured reaction product of: (i) from 45 to 80 percent, based upon total weight of the composition, of an oligomer of the formula: ##STR5## where R 1 is a linear or branched hydrocarbon polymer of from 1,000 to 4,000 molecular weight selected from the group consisting of fully hydrogenated 1,2-polybutadiene; 1,2-polybutadiene hydrogenated to an iodine number of from 9 to 21; and fully hydrogenated polyisobutylene; R 2 is a linear, branched or cyclic alkylene of from six to twenty carbon atoms; and X and Q are independently either (a) a radical of the formula: ##STR6## wherein R 3 , R 4 , and R 5 are independently hydrogen or methyl, m is an integer from 1 to 10, and p is either zero or one, or (b) a saturated alkyl radical of from nine to twenty carbon atoms, with the proviso that said oligomer must possess at least one acrylate or methacrylate terminal group; (ii) from 20 to 50 percent, based on total weight of the composition, of an acrylate or methacrylate terminated reactive diluent of from 11 to 22 carbon atoms; and (iii) from 0.5 to 5 percent, based upon the total weight of the composition, of a photoinitiator selected from the goup consisting of alpha-hydroxycyclohexylphenyl ketone, diethoxyacetophenone, 1-(4-dodecylphenyl)-2-hydroxy-2-methyl-propan-1-one, 2-hydroxy-2-methyl-1-phenyl-propan-1-one, and mixtures thereof; wherein R 1 and R 2 are free of aromatic, ether, or ester functional groups.
Claim 3
Dependent Claim
27 words
The article of manufacture of claim 1, wherein said reactive diluent comprises a mixture of at least two acrylate-terminated compounds of from 11 to 22 carbon atoms.
Claim 4
Dependent Claim
40 words
The article of manufacture of claim 1, wherein said reactive diluent is selected from the group consisting of lauryl acrylate, lauryl methacrylate, stearyl acrylate, stearyl methacrylate, ethylhexyl acrlate, isodecyl acrylate, hexanediol diacrylate, neopentyl glycol diacrylate, trimethylolpropane triacrylate, and mixtures thereof.
Claim 5
Dependent Claim
19 words
The article of manufacture of claim 1, wherein said reactive diluent is a mixture of ethylhexylacrylate and hexanediol diacrylate.
Claim 6
Dependent Claim
15 words
The article of manufacture of claim 1, wherein R 1 consists essentially of hydrogenated 1,2-polybutadiene.
References Cited (Backward Citations)
GB1253757A
Cited
US3678014A
Cited
US3850770A
Cited
US3891523A
Cited
US3872151A
Cited
US3864133A
Cited
US3783151A
Cited
US3852787A
Cited
US4020125A
Cited
US3924023A
Cited
US3907865A
Cited
GB1531351A
Cited
US4137081A
Cited
US4192684A
Cited
US4112017A
Cited
JPS5335481A
Cited
US4204010A
Cited
US4120721A
Cited
US4129667A
Cited
US4135007A
Cited
US4353980A
Cited
GB2070634A
Cited
GB2085023A
Cited
US4333998A
Cited
US4477548A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1991-11-22 | 1992-05-23 | 1992-11-22 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1995-11-22 | 1996-05-23 | 1996-11-22 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1999-11-22 | 2000-05-23 | 2000-11-22 | $7700.00 | Window Closed / Lapsed |