Claims
- 1. A positive-working colored photosensitive recording material for the production of a color test image comprising:
- (a) a temporary layer carrier,
- (b) a release layer comprising polyvinyl alcohol on the surface of said temporary layer carrier,
- (c) a photosensitive layer, with a layer weight of about 0.5-5.0 g/m.sup.2, said layer comprising, in an admixture;
- (i) a dyestuff or pigment,
- (ii) a binder in an amount of about 20-75 weight percent based on the non-volatile contents of said photosensitive layer, said binder comprising a novolak-free phenolic polymer resin, a reaction product of said phenolic polymer resin with a monoisocyanate or a mixture thereof, and
- (iii) an esterification product of a compound containing at least one phenolic hydroxyl group and o-quinonediazide-4-sulfonyl chloride, said esterification product being present in an amount of about 10-30 weight percent based on the nonvolatile constituents of said photosensitive layer, and
- (d) an adhesive layer activatable by means of heat which comprises an alkali-insoluble organic polymer and an alkali-soluble polyester, wherein said alkali-insoluble organic polymer is present in about 70-99 weight percent and said alkali-soluble polyester is present in about 1-30 weight percent in said adhesive layer.
- 2. A recording material as claimed in claim 1, wherein said release layer comprises a partly hydrolyzed polyvinyl acetate.
- 3. A recording material as claimed in claim 2, wherein said partly hydrolyzed polyvinyl acetate has a degree of hydrolysis of about 80 to 90 mol percent.
- 4. A recording material as claimed in claim 2, wherein said release layer consists essentially of a partly hydrolyzed polyvinyl acetate.
- 5. A recording material as claimed in claim 1, wherein said binder comprises a polymer resin comprising units according to the formula I: ##STR5## in which R.sub.1 is hydrogen or a methyl group,
- A is a single bond or the group ##STR6## B is an optionally substituted mono- or polynuclear carbocyclic aromatic ring system,
- p is 1 or 2.
- 6. A recording material as claimed in claim 5, wherein said binder comprises a polymer resin according to the formula I in which
- R.sub.1 is hydrogen or a methyl group,
- A is a single bond or the group ##STR7## and B is phenylene or naphthylene, which can be substituted by lower alkyl, lower alkoxy, aryl or halogen.
- 7. A recording material as claimed in claim 5, wherein said binder comprises a polymer resin comprising units of formula I from about 60 to 100 mol percent.
- 8. A recording material as claimed in claim 5, wherein said binder is selected from the group consisting of homopolymers of pyrocatechol monomethacrylate, resorcinol monomethacrylate, hydroquinone methacrylate and 4-hydroxy-styrene, copolymers thereof and mixtures thereof.
- 9. A recording material as claimed in claim 1, wherein said binder further comprises units according to the formula II:
- --(CHR.sub.2 --CR.sub.3 R.sub.4)-- (II)
- in which
- R.sub.2 is hydrogen or a carboxyl group,
- R.sub.3 is hydrogen, alkyl or a halogen atom,
- R.sub.4 is alkyl, alkoxy, alkoxycarbonyl, acyl, acyloxy, aryl, formyl, cyano, carboxyl or hydroxyl, and if R.sub.2 is a carboxyl group, can be bonded thereto to form an acid anhydride.
- 10. A recording material as claimed in claim 9, wherein said binder comprises units according to the formula II
- --(CHR.sub.2 --CR.sub.3 R.sub.4)-- (II )
- in which
- R.sub.2 is hydrogen or a carboxyl group,
- R.sub.3 is hydrogen, (C.sub.1 -C.sub.12)alkyl, or a halogen atom,
- R.sub.4 is alkyl, alkoxy, alkoxycarbonyl, acyl, acyloxy, aryl, formyl, cyano, carboxyl or hydroxyl, and if R2 is a carboxyl group, can be bonded thereto to form an acid anhydride.
- 11. A recording material as claimed in claim 9, wherein said binder comprises a polymer resin comprising units of formula II from about 0 to 40 mol percent.
- 12. A recording material as claimed in claim 1, wherein said binder is a reaction product of a novolak-free phenolic polymer resin with a monoisocyanate.
- 13. A recording material as claimed in claim 12, wherein said monoisocyanate is phenyl isocyanate.
- 14. A recording material as claimed in claim 12, wherein said monoisocyanate is present in an amount from 0 to about 30 percent by weight, based on the polymer present.
- 15. A recording material as claimed in claim 1, wherein said binder is present in an amount from about 30 to 70 percent by weight, based on the nonvolatile contents of the photosensitive layer.
- 16. A recording material as claimed in claim 1, wherein said esterification product is an esterification product of 1,2-naphthoquinone 2-diazide-4- or 5-sulfonic acid chloride with 2,3,4-trihydroxybenzophenone, bisphenol A or 4-tert.-butylphenol.
- 17. A recording material as claimed in claim 16, wherein said esterification product is an esterification product of 1,2-naphthoquinone 2-diazide-4-sulfonic acid chloride with 2,3,4-trihydroxybenzophenone.
- 18. A recording material as claimed in claim 1, wherein the color of said dye or pigment is a base color selected from the group consisting of cyan, magenta, yellow and black.
- 19. A recording material as claimed in claim 1, wherein said adhesive layer comprises a styrenebutadiene copolymer and an alkali-soluble polyester.
- 20. A recording material as claimed in claim 1, wherein said adhesive layer comprises about 60-95 percent by weight of styrene-butadiene copolymer and about 5-40 percent by weight of said alkali-soluble polyester.
Priority Claims (1)
Number |
Date |
Country |
Kind |
4006856 |
Mar 1990 |
DEX |
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Parent Case Info
The present application is a continuation-in-part of U.S. Ser. No. 07/664,753 filed Mar. 5, 1991 now abandoned.
US Referenced Citations (7)
Foreign Referenced Citations (5)
Number |
Date |
Country |
0115899 |
Aug 1984 |
EPX |
0165030 |
Dec 1985 |
EPX |
0357324 |
Mar 1990 |
EPX |
1550524 |
Aug 1979 |
GBX |
8606182 |
Oct 1986 |
WOX |
Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
664753 |
Mar 1991 |
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