CA1112092A - Light-sensitive copying composition including a branched polyurethane prepolymer with free terminal isocyanate groups - Google Patents
Light-sensitive copying composition including a branched polyurethane prepolymer with free terminal isocyanate groupsInfo
- Publication number
- CA1112092A CA1112092A CA286,118A CA286118A CA1112092A CA 1112092 A CA1112092 A CA 1112092A CA 286118 A CA286118 A CA 286118A CA 1112092 A CA1112092 A CA 1112092A
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- CA
- Canada
- Prior art keywords
- acid
- copying composition
- composition according
- copying
- light
- Prior art date
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Classifications
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/016—Diazonium salts or compounds
- G03F7/021—Macromolecular diazonium compounds; Macromolecular additives, e.g. binders
- G03F7/0212—Macromolecular diazonium compounds; Macromolecular additives, e.g. binders characterised by the polymeric binder or the macromolecular additives other than the diazo resins or the polymeric diazonium compounds
- G03F7/0217—Polyurethanes; Epoxy resins
Abstract
LIGHT-SENSITIVE COPYING COMPOSITION
Abstract of the Disclosure This invention relates to a light-sensitive copying composition comprising a diazonium salt condensation product, a stabilizer, and a polyurethane prepolymer with free terminal isocyanate groups.
Abstract of the Disclosure This invention relates to a light-sensitive copying composition comprising a diazonium salt condensation product, a stabilizer, and a polyurethane prepolymer with free terminal isocyanate groups.
Description
1~1;2~92 K-2487 This invention rclal:cs to a ne4ative-~,vorking light-sensitive copying composition ~,vhicn may be used for th2 manufacture of hi~h-quality planographic printing plates, proofing films, color separations, stencils, and etch resists.
Hitherto, two alternatives have been proposed for solving t'ne technical problems involved in the provision of high-q~lality negative-working planographic printing plates based on diazonium compounds.
One of these alternatives is concerned with the improvement of the properties of the light-sensitive diazo compound, whereas the othér is aimed at the discovery of novel, sometimes tailor-made polymers which serve as a supporting frame in the copying composition and impart their physical properties thereto.
Whereas the known light-sensitive diazo compounds, such as those disclosed in German Offenlegungsschriften No. 2,024,2~2, and No. 2,024,244, have attained a high level of quality, the fine adjust-ment of the properties of copying compositions by means of polymers added thereto was found to be extremely difficult. There is a risk, for example, that the resistance to abrasion is insufficent for high demands, e.g. for cardboard printing, or that the image areas become blinded due to a loss of oleophilic properties, or that scumming occurs due to un-satisfactory development, or that thc various components of the layer are not compatible with each other under changing conditions of storage.
It is known from U. S. Patent No. 3,660,097, to combine linear polyurethane resins with ne~ative-working or positive-working diazo compounds in light-sensitive copying compositions. Such copying compositions have the following drawbacks, however:
Difficulties in thc preparation of the coating solutions due to the poor sol lbility of thc layer components in the selccted solvcnts;
Hitherto, two alternatives have been proposed for solving t'ne technical problems involved in the provision of high-q~lality negative-working planographic printing plates based on diazonium compounds.
One of these alternatives is concerned with the improvement of the properties of the light-sensitive diazo compound, whereas the othér is aimed at the discovery of novel, sometimes tailor-made polymers which serve as a supporting frame in the copying composition and impart their physical properties thereto.
Whereas the known light-sensitive diazo compounds, such as those disclosed in German Offenlegungsschriften No. 2,024,2~2, and No. 2,024,244, have attained a high level of quality, the fine adjust-ment of the properties of copying compositions by means of polymers added thereto was found to be extremely difficult. There is a risk, for example, that the resistance to abrasion is insufficent for high demands, e.g. for cardboard printing, or that the image areas become blinded due to a loss of oleophilic properties, or that scumming occurs due to un-satisfactory development, or that thc various components of the layer are not compatible with each other under changing conditions of storage.
It is known from U. S. Patent No. 3,660,097, to combine linear polyurethane resins with ne~ative-working or positive-working diazo compounds in light-sensitive copying compositions. Such copying compositions have the following drawbacks, however:
Difficulties in thc preparation of the coating solutions due to the poor sol lbility of thc layer components in the selccted solvcnts;
2 k~--2 4 ~ 7 insufficient differentiation bet~,~7een the image areas an(l the non-imaye areas; poor developability and resulting undesirable scumming during printing; the so-called "aqueous" developers used contain large quan-tities of solvents and thus are more or less harmful ecologically, or cause annoying odors; and low practical light-sensitivity.
The light-sensitive coating composition known from German Offenlegungsschrift No. 2 ,361,931, contains branched polyurethane resins; it is expressly stated in this publication, however, that these eompounds are produced by the complete reaction of the isocyanate groups contained in the starting materials, so that the resin does not contain any free, terminal isocyanate groups.
It is the object of the present invention to provide a light-sensitive copying composition based on diazo eompounds whieh does not have the drawbael~s just mentioned and which, above all, has good storage properties, a high praeti~al light-sensitivity, enables good differentiation between image areas and non-image areas, results in a high resolution eapaeity, guarantees an easy and seum-free develop-ment, may be developed without environmental hazards, produees long runs and forms a durable, elastie eoating after exposure which is free of pores and is resistant to meehanieal abrasion and chemical attack.
Aecording to the present invention, this object is achieved by a li~ht-sensitive copying composition which comprises a diazonium salt condensation product and a polyurethane and in which the polyure-thane is a branched polyurethane prepolymer containing free terminal isocyanate groups; the copying composition further contains a stabilizer.
The preferred copying composition according to the present in-vention contains, as the substantial components, a negative-working light-sensitive diazonium compound which dissolves readily in a sol-vent, a thermosetting po!yurcthane compound with free terminal :~ ~1 2 ~ ~ 2 ~ 7 isocyanate ~Jroups, a stabilizer of acid character, and r)ossibly a non-drying alkyd resin.
Light-sensitive diazoniurn compounds which may be used are, above all, the diazo condensates produced from diazotized p-amino-diaryl-amines and carbonyl yroup-containing compounds, such as alde-hydes, preferably formaldehyde, or aldehyde-donors, e.g. paraformal-dehyde, which are described in various reprographic systems . These and other suitable compounds are disclosed in German Patent No.
1,214,086, and in U. S. Patents Nos. 2,922,715 and 2,946,683.
Diazonium compounds which are particularly suitable are con-densation products of an aromatic diazonium compound according to German Offenlegungsschrift No. 2,024,244 comprising at least one unit each of the general types A(-D) and B
which are linked by a bivalent intermediate member derived from a car-bonyl compound capable of condensation, and wherein A is the radical of a compound containing at least two carbocyclic and/or heterocyclic aromatic rings and being capable of condensation in at least one position of its molecule with an active carbonyl compound in an acid medium, D is a diazonium salt group linked to an aromatic carbon atom of A, n is an integer from 1 to 10, and B is a radical of a compound free of diazonium groups and capable of condensatiGn in at least one position of its molecule with an active carbonyl compound in an acid medium.
2 ~.-2~37 Virtually 211 compounds may ~e usecl as components A(-D) and B which are capable of reaction, with condensation, with active car-bonyl com?ounds in an acid medium and which are not decomposed by the conditions of the condensation reaction.
The condensation products are prepared either by a joint conden-sation of compounds corresponding to formula A(-D)n and compounds eorresponding to formula B with an active carbonyl compound, prefer-ably formaldehyde, or by condensation of A(-D)n with compounds B
eorresponding to the general formula 10E (-CHRa-ORb) m wherein E is a residue obtained by the splitting-off of m hydrogen atoms from a compound B of the above indicated meaning, Ra is H, alkyl, preferably alkyl with 1 to ~ earbon atoms, or aryl j preferably phenyl, Rb is H, alkyl or aeyl, preferably with 1 to 4 earbon atoms, or phenyl, and m is an integer from 1 to 10.
20Diazonium Compounds Corresponding to A(-D)n In addition to the aromatie iso- or heterocyelie group whieh earries the diazo group, the diazonium compounds to be used in aceord-anee with the present invention contain in the radical ~ at least one further isocyelic and/or heterocyelic ring which contains at least one nuclear position capable of condensation.
~ n important group of diazonium compounds whicl; are preferred as reaction partners are compounds of the following ~eneral formula:
(Rl-R3-)p R2 - N2X
1~1 2~!~Z K - 2 4 8 7 w'nerein p is a positive integer from 1 to about 3, preferably 1, X is the anion of the diazonium compound, which also may be formed by an acid substituent of the molecule, Rl is a substituted or unsubstituted isocyclic or hetero-cyclic aromatic residue which has at least one posi-tion capable of condensation, preferably a phenyl radical which may be substituted. Preferred substitu-ents are, e.g., alkyl, alkoxy, alkylmercapto, aryloxy, arylmercapto, hydroxy, mercapto, amino, and anilino group s, R2 is an aromatic ring of the benzene or naphthalene series which may carry further substituents, in addition to the diazoniurn group, and R3 is a connecting member between members Rl and R2, the connecting member corresponding, e.g., to one of the following types, the ring Rl always being imagined at the left-hand side and the group R2 at the right-hand side, unless R3 is symmetrical:
a simple homopolar bond, ~(CH2)q~NR4~ (wherein q is a whole number from 0 to 5, and R4 is H, alkyl with 1 to 5 carbon atoms, aralkyl with 7 to 12 carbon atoms, or aryl with 6 to 12 carbon atoms), ~(CII2)q~NR4~(C~12)r~NR5~ (wherein r is a whole number from 2 to 5 and R5 is H or alkyl with 1 to 5 carbon atoms), ~~(CH2)q~NR~~(C~T2)r~NR5~ (same definition) . -~487 1~1;2~gZ
( ~ 2)r 4 S (C~2)r 4 O R6 (wherein R6 is ar~lene with 6 to 12 carbon atoms --O----S---SO -NR
-S-(C~2) -CO-NR4-Exemplary of compounds of the formula (Rl-R3-)pR2-N2X are:
2, 3 ', 5-trimethoxy-diphenyl-4-diazoniumchloride 2, 4 ', 5 -triethoxy-diphenyl-4-diazoniumchloride 4-~3-(3-methoxy-phenyl)-propylamin~-benzenediazoniumsulfate 4-[N-ethyl-N-(4-methoxy-benzyl)-amin~-benzenediazoniumchloride 4-[N-(naphthyl-(2)-methyl)-N-n-propyl-amin~-benzenediazoniumsulfate 4- ~N - (3 -phenoxy-propyl)-N-methyl-amin~ -2, 5 -dimethoxy-benzene-diazoniumtetrafluoroborate 4-LN-(3-phenyl-mercapto-propyl)-N-ethyl-amino]-2-chloro-5-methoxy-benzenediazoniumchloride 2 0 4- [4- (3 - methyl-phenoxy)-phenoxy~- 2, 5 -dimethoxy-benz e ne-diazonium-sulfate, 4- (4 - methoxy-phenylmercapto) -2, 5 -diethoxy-benzenediazoniumchloride 2, 5-diethoxy-4-phenoxy-benzenediazoniumchloride 4-(3, 5-dimethoxy-benzoylamino)-2, 5-diethoxy-benzenediazonium-hexafluorophosphate :
carbazole-3 -diazoniumchloride
The light-sensitive coating composition known from German Offenlegungsschrift No. 2 ,361,931, contains branched polyurethane resins; it is expressly stated in this publication, however, that these eompounds are produced by the complete reaction of the isocyanate groups contained in the starting materials, so that the resin does not contain any free, terminal isocyanate groups.
It is the object of the present invention to provide a light-sensitive copying composition based on diazo eompounds whieh does not have the drawbael~s just mentioned and which, above all, has good storage properties, a high praeti~al light-sensitivity, enables good differentiation between image areas and non-image areas, results in a high resolution eapaeity, guarantees an easy and seum-free develop-ment, may be developed without environmental hazards, produees long runs and forms a durable, elastie eoating after exposure which is free of pores and is resistant to meehanieal abrasion and chemical attack.
Aecording to the present invention, this object is achieved by a li~ht-sensitive copying composition which comprises a diazonium salt condensation product and a polyurethane and in which the polyure-thane is a branched polyurethane prepolymer containing free terminal isocyanate groups; the copying composition further contains a stabilizer.
The preferred copying composition according to the present in-vention contains, as the substantial components, a negative-working light-sensitive diazonium compound which dissolves readily in a sol-vent, a thermosetting po!yurcthane compound with free terminal :~ ~1 2 ~ ~ 2 ~ 7 isocyanate ~Jroups, a stabilizer of acid character, and r)ossibly a non-drying alkyd resin.
Light-sensitive diazoniurn compounds which may be used are, above all, the diazo condensates produced from diazotized p-amino-diaryl-amines and carbonyl yroup-containing compounds, such as alde-hydes, preferably formaldehyde, or aldehyde-donors, e.g. paraformal-dehyde, which are described in various reprographic systems . These and other suitable compounds are disclosed in German Patent No.
1,214,086, and in U. S. Patents Nos. 2,922,715 and 2,946,683.
Diazonium compounds which are particularly suitable are con-densation products of an aromatic diazonium compound according to German Offenlegungsschrift No. 2,024,244 comprising at least one unit each of the general types A(-D) and B
which are linked by a bivalent intermediate member derived from a car-bonyl compound capable of condensation, and wherein A is the radical of a compound containing at least two carbocyclic and/or heterocyclic aromatic rings and being capable of condensation in at least one position of its molecule with an active carbonyl compound in an acid medium, D is a diazonium salt group linked to an aromatic carbon atom of A, n is an integer from 1 to 10, and B is a radical of a compound free of diazonium groups and capable of condensatiGn in at least one position of its molecule with an active carbonyl compound in an acid medium.
2 ~.-2~37 Virtually 211 compounds may ~e usecl as components A(-D) and B which are capable of reaction, with condensation, with active car-bonyl com?ounds in an acid medium and which are not decomposed by the conditions of the condensation reaction.
The condensation products are prepared either by a joint conden-sation of compounds corresponding to formula A(-D)n and compounds eorresponding to formula B with an active carbonyl compound, prefer-ably formaldehyde, or by condensation of A(-D)n with compounds B
eorresponding to the general formula 10E (-CHRa-ORb) m wherein E is a residue obtained by the splitting-off of m hydrogen atoms from a compound B of the above indicated meaning, Ra is H, alkyl, preferably alkyl with 1 to ~ earbon atoms, or aryl j preferably phenyl, Rb is H, alkyl or aeyl, preferably with 1 to 4 earbon atoms, or phenyl, and m is an integer from 1 to 10.
20Diazonium Compounds Corresponding to A(-D)n In addition to the aromatie iso- or heterocyelie group whieh earries the diazo group, the diazonium compounds to be used in aceord-anee with the present invention contain in the radical ~ at least one further isocyelic and/or heterocyelic ring which contains at least one nuclear position capable of condensation.
~ n important group of diazonium compounds whicl; are preferred as reaction partners are compounds of the following ~eneral formula:
(Rl-R3-)p R2 - N2X
1~1 2~!~Z K - 2 4 8 7 w'nerein p is a positive integer from 1 to about 3, preferably 1, X is the anion of the diazonium compound, which also may be formed by an acid substituent of the molecule, Rl is a substituted or unsubstituted isocyclic or hetero-cyclic aromatic residue which has at least one posi-tion capable of condensation, preferably a phenyl radical which may be substituted. Preferred substitu-ents are, e.g., alkyl, alkoxy, alkylmercapto, aryloxy, arylmercapto, hydroxy, mercapto, amino, and anilino group s, R2 is an aromatic ring of the benzene or naphthalene series which may carry further substituents, in addition to the diazoniurn group, and R3 is a connecting member between members Rl and R2, the connecting member corresponding, e.g., to one of the following types, the ring Rl always being imagined at the left-hand side and the group R2 at the right-hand side, unless R3 is symmetrical:
a simple homopolar bond, ~(CH2)q~NR4~ (wherein q is a whole number from 0 to 5, and R4 is H, alkyl with 1 to 5 carbon atoms, aralkyl with 7 to 12 carbon atoms, or aryl with 6 to 12 carbon atoms), ~(CII2)q~NR4~(C~12)r~NR5~ (wherein r is a whole number from 2 to 5 and R5 is H or alkyl with 1 to 5 carbon atoms), ~~(CH2)q~NR~~(C~T2)r~NR5~ (same definition) . -~487 1~1;2~gZ
( ~ 2)r 4 S (C~2)r 4 O R6 (wherein R6 is ar~lene with 6 to 12 carbon atoms --O----S---SO -NR
-S-(C~2) -CO-NR4-Exemplary of compounds of the formula (Rl-R3-)pR2-N2X are:
2, 3 ', 5-trimethoxy-diphenyl-4-diazoniumchloride 2, 4 ', 5 -triethoxy-diphenyl-4-diazoniumchloride 4-~3-(3-methoxy-phenyl)-propylamin~-benzenediazoniumsulfate 4-[N-ethyl-N-(4-methoxy-benzyl)-amin~-benzenediazoniumchloride 4-[N-(naphthyl-(2)-methyl)-N-n-propyl-amin~-benzenediazoniumsulfate 4- ~N - (3 -phenoxy-propyl)-N-methyl-amin~ -2, 5 -dimethoxy-benzene-diazoniumtetrafluoroborate 4-LN-(3-phenyl-mercapto-propyl)-N-ethyl-amino]-2-chloro-5-methoxy-benzenediazoniumchloride 2 0 4- [4- (3 - methyl-phenoxy)-phenoxy~- 2, 5 -dimethoxy-benz e ne-diazonium-sulfate, 4- (4 - methoxy-phenylmercapto) -2, 5 -diethoxy-benzenediazoniumchloride 2, 5-diethoxy-4-phenoxy-benzenediazoniumchloride 4-(3, 5-dimethoxy-benzoylamino)-2, 5-diethoxy-benzenediazonium-hexafluorophosphate :
carbazole-3 -diazoniumchloride
3-methoxy-diphenyleneoxide-2-diazoniumchloride diphenyla~4ine-4-diazoniumsulfate .
'~
K-24~7 g2 Mixed coi~clensates particularly suitable for use in the reproduc-tion layers oE the inv2ntion are obtainecl by using diazo compounds of the general formula (Rl-R3-)p R2-N2X
wherein p is an integer from 1 to 3, preferably 1, Rl is a phenyl group cither unsubs ituted or substituted by one or more alkyl or alkoxy groups, R2 is a benzene ring which, in addition to the diazonium group, may carry one or two identical or different sub-stituents which may be halogen atoms, alkyl groups with 1 to 4 carbon atoms, or alkoxy groups with 1 to 5 carbon atoms, and R3 is a homopolar bond or one of the members -O-, -S-, or -NH - .
A particularly important group of diazo compounds having struc-tures according to the general formula (Rl-R3-)pR2-N2X are the salts of the diphenylamine-4-diazonium ion and its substitution products.
Preferably employed substituents which may be linked to the phenyl nuclei of the diphenylamine-4-diazonium compounds are alkyl and alkoxy groups with 1 to 6, preferably 1 to 2, carbon atoms. Fur-thermore, the halogens and the following groups may be employed:
-COOR (R is H, alkyl or aryl) -CN
-COR (R is ~-1, alkyl or aryl) -S2R (R is H, alkyl, or aryl) -NHCOR (R is alkyl or aryl) -NHR ancl NRR' (R and R' are alkyl, aryl, or aralkyl).
Z K - 2 ~ ~ 7 E~empl;lry of substituents ~/hich may be linkecl to the phenyl nuclei of the cliphenylamine diazonium group are methyl, propyl, iso-butyl, trifluoromethyl, methoxy, di:Eluoromethoxy, etho~y, hydroxy-ethoxy, ethoxyethoxy, fluorine, chlorine, bromine, iodine, ethoxycar- ~ ' bonyl, phenoxycarbonyl, acetyl, methoxysulfonyl, ethoxysulfonyl, acetylamino, methylamino, ethylamino, dimethylamino, diethylamino, methylethylamino, phenylamino, benzylamino, methylbenzylamino, and ethylbenzylamino .
Suitable diphenylamine-4-diazonium salts are, for example, the diazonium salts derived from the following amines: 4-amino-diphenyla-mine, 4-amino-3-methoxy-diphenylamine, 4-amino-2-methoxy-di-phenylamine, 4'-amino-2-methoxy-diphenylamine, 4'-amino-4-methoxy-diphenylamine, 4-amino-3-methyl-diphenylamine, 4-amino-3-ethyl-diphenylamine, 4'-arnino-3-methyl-diphenylamine, 4'-amino-4-methyl-diphenylamine, 4-amino-3-ethoxy-diphenylamine, 4-amino-3-hexyl-oxy-diphenylamine, 4-amino-3-~-hydroxy-ethoxy-diphenylamine, 4'-amino-2-methoxy-5-methyl-diphenylamine, 4-amino-3-methoxy-~- :
methyl-diphenylamine, 4'-amino-3,3'-dimethyl-diphenylamine, 3'-chloro-4-amino-diphenylamine, 4'-amino-4-n-butoxy-diphenylamine,
'~
K-24~7 g2 Mixed coi~clensates particularly suitable for use in the reproduc-tion layers oE the inv2ntion are obtainecl by using diazo compounds of the general formula (Rl-R3-)p R2-N2X
wherein p is an integer from 1 to 3, preferably 1, Rl is a phenyl group cither unsubs ituted or substituted by one or more alkyl or alkoxy groups, R2 is a benzene ring which, in addition to the diazonium group, may carry one or two identical or different sub-stituents which may be halogen atoms, alkyl groups with 1 to 4 carbon atoms, or alkoxy groups with 1 to 5 carbon atoms, and R3 is a homopolar bond or one of the members -O-, -S-, or -NH - .
A particularly important group of diazo compounds having struc-tures according to the general formula (Rl-R3-)pR2-N2X are the salts of the diphenylamine-4-diazonium ion and its substitution products.
Preferably employed substituents which may be linked to the phenyl nuclei of the diphenylamine-4-diazonium compounds are alkyl and alkoxy groups with 1 to 6, preferably 1 to 2, carbon atoms. Fur-thermore, the halogens and the following groups may be employed:
-COOR (R is H, alkyl or aryl) -CN
-COR (R is ~-1, alkyl or aryl) -S2R (R is H, alkyl, or aryl) -NHCOR (R is alkyl or aryl) -NHR ancl NRR' (R and R' are alkyl, aryl, or aralkyl).
Z K - 2 ~ ~ 7 E~empl;lry of substituents ~/hich may be linkecl to the phenyl nuclei of the cliphenylamine diazonium group are methyl, propyl, iso-butyl, trifluoromethyl, methoxy, di:Eluoromethoxy, etho~y, hydroxy-ethoxy, ethoxyethoxy, fluorine, chlorine, bromine, iodine, ethoxycar- ~ ' bonyl, phenoxycarbonyl, acetyl, methoxysulfonyl, ethoxysulfonyl, acetylamino, methylamino, ethylamino, dimethylamino, diethylamino, methylethylamino, phenylamino, benzylamino, methylbenzylamino, and ethylbenzylamino .
Suitable diphenylamine-4-diazonium salts are, for example, the diazonium salts derived from the following amines: 4-amino-diphenyla-mine, 4-amino-3-methoxy-diphenylamine, 4-amino-2-methoxy-di-phenylamine, 4'-amino-2-methoxy-diphenylamine, 4'-amino-4-methoxy-diphenylamine, 4-amino-3-methyl-diphenylamine, 4-amino-3-ethyl-diphenylamine, 4'-arnino-3-methyl-diphenylamine, 4'-amino-4-methyl-diphenylamine, 4-amino-3-ethoxy-diphenylamine, 4-amino-3-hexyl-oxy-diphenylamine, 4-amino-3-~-hydroxy-ethoxy-diphenylamine, 4'-amino-2-methoxy-5-methyl-diphenylamine, 4-amino-3-methoxy-~- :
methyl-diphenylamine, 4'-amino-3,3'-dimethyl-diphenylamine, 3'-chloro-4-amino-diphenylamine, 4'-amino-4-n-butoxy-diphenylamine,
4'-amino-3' ,4-dimethoxy-diphenylamine, 4-amino-diphenylamine-2-sulfonic acid, 4-amino-diphenylamine-2-carboxylic acid, 4-amino-diphenyl-amine-2'-carboxylic acid, and 4'-bromo-4-amino-diphenyl-amine .
Preferably employed are 4-amino-diphenylamine and 3-methyl-4-amino-diphenylamine, particularly preferably are the 3-alkoxy-4-amino-diphenylamines having 1 to 3 carbon atoms in the alkoxy group, especi-ally the 3-methoxy-4-amino-diphenylamine.
Components B
Similarly, a plurality of compounds are suitable as components B
K~2'1 87 in the pr~paration of the mixed condensates. An important class are the substituted or unsubstituted aromatic hyclrocarbons and aromatic hetero-cyclic compounds.
Examples of unsubstituted aromatic isocyclic and heterocyclic compounds which may be used as components B are, e.g., benzene, naphthalene, anthracene, phenanthrene, pyrene, indene, fluorene, acenaphthene, thiophene, furan, benzofuran, diphenylene oxide, benzo-thiophene, acridine, carbazole, phenothiazine, and others which may be substituted by one of the following groups:
-N (R8) 2 wherein R7 may be H, -CO-alkyl, -CO-aryl, -CO-heteroyl, -CO-aralkyl, -S02-alkyl, -S02-aryl, -S02-aralkyl, -S02-heteroyl, -CONH2, -CSNH2, -CONH-alkyl, -CONH-aryl, -CO-O-alkyl, -CO-O-aryl, -CS-O-aryl, and-CS-O-alkyl, and R8 may be H, an alkyl, aryl, or an aralkyl group.
The meanings of certain terms are as follows:
Alkyl: A branched or unbranched alkyl group with 1 to 10 carbon atoms which may be substituted, e.g. by -halo~en, -alkoxy, -OH, -COOH, -CONH2, -CN, -CO-CH3, -S03H, or -P03H2, or hyclro~ens in nei~hborin~ positions may be replaced by oxy~en (epcxides) or _ g _ K-~4~7 r~moved (multiple bonds). The alkyl radic~l also may be interrupted, e . g . by -O , -S-, -N (alkyl)-, -SO2-, or -SO- .
Aryl: A mono- or polynuclear aromatic ring which, includiny alkyl, alkoxy, or aralkyl ~roups which may be linked thereto, contains from 6 to 20 carbon atoms. The aryl nucleus may carry additional sub-stituents .
Aralkyl: A group containing 7 to 20 carbon atoms which is com-posed of alkyl and aryl radicals (corresponding to the above definition).
Alkoxy: O-alkyl group, the alkyl having the above meaning.
The alkyl, aryl, aralkyl, and alkoxy groups may be present one or more times, either alone or together.
According to the above, the compounds to be employed as com-ponents B or components Bl derived therefrom belong to the following groups of substances; for example:
aromatic compounds (iso- and heterocyclic), unsubstituted aromatic amines phenols and thiophenols phenol ethers and thiophenol ethers aromatic compounds substituted by alkyl, aralkyl or aryl groups urea, thiourea, carboxylic acid amides (aliphatic and aromatic), and sulfonie acid amides (aliphatie and aromatie).
In order to limit the eontribution of these substances to the molecular weight of B, the proportion of the four above-mentioned sub-stituents in the structure of the molecule of compound B is limited, the primary aromatic iso- or heterocyclic ring or the condensed ring system being substituted only to such an extent that the aromatic compound is increased, in the case of substitution by alkyl groups: by not more than 10 carbon atoms, by aryl groups: by not more than 20 carbon atoms, ~--2!-~37 g2 by aralkyl groups: by not more than 20 carbon atoms, and by alkoxy groups: by not more than 10 carbon atoms.
The total increase in C atoms by these four types of substituents should not exceed 30 C atoms with respect to the original aromatic nucleus .
Generally, components B are preferred which have a molecular weight of less than 500, preferably less than 250, amines being calcu-lated as free amines, not in the salt form, and acid groups being calcu-lated in the H-form. If the compounds are aromatic compounds, those compounds are preferred within these limits which contain not more than 4, preferably not more than 1 to 2, most advantageously 2, individual aromatic rings (fused to each other and/or connected with each other, preferably by homopolar bonds and/or intermediate members).
This means that the number of substituents with longer chains, i.e. those having a relatively large number of C atoms, which may be present at the same time, is smaller than the number of substituents with fewer C àtoms. C~enerally, the short-chain alkyl and alkoxy groups tl to 4 carbon atoms) and the smaller aromatic radicals in aryl and aral-kyl groups (up to 12 carbon atoms) are preferred, because the corre-sponding compounds are more easily soluble in the condensation media and condensation thus can be performed more easily. For the same reason, substitution is limited as described above.
The condensable iso- or heterocyclic aromatic rings also may have substituents exerting a deactivating effect on the nuclei, e.g.
O2N-, HOOC-, NC-, HO3S, and H2O3P ~roups, provided these groups do not destroy the condensability of these rings. This means that such substituents may be particularly introduced if the ring as SUCIl is easily condensable or carries substituents having a strongly activating cffect.
Another possibility for introducing deactivatin~ substituents without Z
unduly reducing the condensability of the ring is to place the substitu-ents in side chains, e.g. aliphatic side chains.
Substituents deactivating nuclear condensation also may be present in those cases in which the reactivity of the condensable nuc-leus is not necessary, because the nucleus has substituents at which condensation can take place. Such substituents are listed above and include, for example, the groups -CO-NH2, -SO2NH2, and -SO2NH-alkyl .
Of the classes of compounds indicated, from which the compounds B and Bl derive, generally those are preferred which are unsaponsifiable or only difficultly saponifiable under acid condensation conditions. The same applies to the diazo compounds A(-D) .
For this reason, those compounds B or 81 of the series of aro-matic iso- and heterocyclic compounds are advantageous which are either unsubstituted or carry alkyl, aralkyl, aryl, alkoxy, alkylmercapto, aryloxy, arylmercapto, OH, SO, and amino groups as substituents, if desired, in addition to unsaponifiable deactivating substituents, e.g.
COOh. Of these compounds, those aromatic iso- and heterocyclic compounds are particularly preferred which are unsubstituted or contain, as substituents, one or more alkyl, aralkyl, aryl, alkoxy, alkylmercap-to, arylmercapto, and aryloxy groups, particularly when condensates are desired which should not contain salt-forming ~roups other than the . .
diazo group.
Exemplary of particularly suitable compounds B or ~1 are those which are derived from diphenyl ether, diphenyl sulfide, diphenyl methane, or diphenyl, and may contain one or two substituents selected from halogen atoms, alkyl ~roups, and allcoxy ~roups, but are prefer-ably unsubstituted.
If thesc compounds arc condensed with diphenylamirle-~-diazonium salts which are unsubstit~ltcd or substituted by a lower a,kyl , 1~12~g2 group or a lo~ver alkoxy group containing up to 3 carbon atoms, mixed condensates are obtained which can be readily precipitated and in good yields in the form oE the salts of hyclrochloric acid, hydrobromic acid, or of suitable sulfonic acids, especially when the component B or B1 is employed in a proportion from 0.5 to 2 moles per mole of diazo compound.
The new condensation products of the invention generally contain 0.1 to 50 moles, preferably 0.1 to 20 moles, on the average, of units of component B per mole of units of component A(-D)n. A particularly pre-ferred range is from 0.2 to 2 moles of B per mole of A(-D) .
The mixed diazo condensates known fromGerm~n Offenlegungs-schrift No. 2 ,041,395, i.e. condensation products in which the anion of the diazonium salt is derived from an aliphatic monosulfonic acid with 1 to 6 carbon atoms, are particularly suitable for the copying composition according to the present invention.
The aliphatic monosulfonic acids forming the anion of the diazon-ium condensates used according to the invention normally have bet~veen 1 and 6 carbon atoms and may be substituted, if desired, by substitu-ents which are not too heavy, e.g. halogen atoms, viz. fluorine, chlorine, bromine or iodine, hydroxy groups, ether groups, and the like.
Normally, not more than 1 substituent is present. The aliphatic chain may be straight, branched, or annular and may also contain double bonds.
Methane sulfonates are particularly preferred.
The polyurethane prepolymers with free terminal isocyanate groups used according to the present invention normally are composed of three components, viz. a diisocyanate (I), a polyol ~vith at least three free OH groups (II), and a diol (III).
Suitable diisocyanates (I) are: 2,4-toluylene diisocyanate, 2,6-toluylene diisocyanate, 4,4'-diphenylmethane diisocyanate, isophoron-diisocyanate, 2 ,2 ,4-trimethyl-hexamethylene diisocyanate, hexamethyl-Qg2 elle cliisocyanate, xylylene diisocyanate, 3,3'-bitoluylene-4,~'-di-isocyanate, 3, 3 ' -dimethyl-cyclohexane-4, 4 ' -diisocyanate, ~, 4 '-pheny l-cyclohexylmetha ne-dii socya nate, 4, 4 ' -dicyclohexyl metha ne -diisocyanate, phenylene-diisocyanate, 4,4'-diphenylether-diisocya-nate, naphthalene-diisocyanate, and Iysine-diisocyanate.
2, 4-Toluylene-dii socyanate, 2, 6-toluyl e ne-diisocya nate, 4, 4 ' -diphenylmethane-diisocyanate, and 2,2,4-trimethyl-hexamethylene-diisocyanate are preferred.
The diisocyanates may be used either alone or in admixturb with each other.
Suitable polyols (II) are, e.g.: 1 ,1,l-trimethylol propane, 1 ,1 ,1-trimethylol ethane, pentaerythritol, dipentaerythritol, and others .
Diols (III) which may be used are, among others, polyalkylene glycols of the following general formula HO(-CHR-CH2-O)n-H
-whereln R stands for H or all~yl, preferably for H or methyl, and n is an integer from 1 to 10, or compounds of the following general formula 2 0 HO-CnH 2 n~OH
wherein n is an integer from 2 to 10.
As a rule, the diisocyanates are reacted in known manner with a deficiency of polyol and diol, so that the proportion of free terminal isocyanate groups in the resulting polyurethane is in the range from 1 to 30 per cent by weight, preferably from 5 to 25 per cent by weight, and most advantageously between 7 and 20 per cent by weight.
Depencliny upon the type and proportion of the polyol component, the polyurethane prepolynlers thus prepared are more or less branched.
.
~-24~7 For stabilization of the copying composition, a eompound ~,vit~
acid character must be added thereto. Suitable acids are mineral acids and also strong organic acids, phosphoric acid, sulfuric acid, perchlor-ic acid, boric acid, and p-toluene sulfonic acid being preferred. Phos-phoric acid is a particularly advantageous acid.
For fine adjustment of the layer properties, a non-drying syn-thetic alkyd resin with a branched, saturated fatty acid component (cf.
Karsten "Lackrohstofftabellen", page 73 et seq.) is added to the copy-ing composition, by which the impact strength of the polyurethane pre-polymer is increased and longer runs become possible, if the copying eomposition is used as a printing image. At the same time, the resin exerts a plasticizing effect on the prepolymer.
Preferred alkyd resins are those which are obtained by polycon-densation of phthalic acid anhydride, polyols, e.g. glycerol, pentaeryth-ritol, 1 ,1 ,1-trimethylol propane, or 1 ,1 ,1-trimethylol ethare, and a branched monocarboxylic acid, e.g. i-nonane acid, i-octane acid, etc.
Further, knownplasticizers, adhesionpromoters, dyestuffs, pigments, eolor couplers, and/or UV absorbers may be added to the eopying compositions of the invention.
The type and quantity of such additives depend on the purpose for which the copying composition according to the invention is des-tined. In any ease, however, care must be taken that the substances added do not absorb an excessive proportion of the actinic light requircd for eross-linking and thus reduce the practical licJht-sensitivity of the eomposition .
Suitable plasticizers are, e.g.: dibutyl phthalate, diisooctyl-adipate, nitro esters, alkyl and aryl phosphate esters, chlorinated paraffins, and glycols or aliphatic polyols.
If it is desired to ensure good storability at relative high atmos-pheric moisture, water-insoluble plasticizers are preferred.
Adhesion promoters are added in those cases where the light-sensitive copying compositions according to the invention are to be ex-posed to p~rticular stress, e.g. when they are to be used as photore-sist materials. Suitable adhesion promoters are, e.g., monomeric or polymeric organic silanes, nitrogen-containing heterocyclic compounds, such as those disclosed in U. S. Patents Nos. 3,645,722, 3,622,234, and 3,827,908, heterocyclic mercaptan compounds according to German Offenlegungsschrift No. 2,028,733, mercapto alkanoic acid anilides according to German Offenlegungsschrift No. 2,448,821, and mercapto alkanoic acid esters according to German Offenlegungsschrift No.
2,448,750.
Further, the light-sensitive copying compositions according to the invention may contain dyestuffs and/or pigments, which may serve to increase the contrast and also to harden the layer. Suitable dye-stuffs are mentioned, e.g., in U. S. Patents Nos. 3,218,167, and 3,884,693.
Rhodamine 6 GND extra (C.I. 45160), Crystal Violet (C.I. 42555), and a blue dyestuff obtained by condensation of 2,4-dinitro-6-chloro-benzene diazonium salt with 2-methoxy-5-acetyl-amino-N-cyanoethyl-N-hydroxy ethyl aniline, are particularly suitable.
MetanilYellow (C.I. 13065) and Methyl Oran~e (C.I. 13025) may be used to increase the image contrast after development.
Further, the copying compositions according to the invention may contain UV-absorbers which serve as anti-halation filters. Suit-able, non-coloring substances are described, e.g., in German Of Een-legungsschrift No . 2,243, J 82.
~?~Z K~24~7 Within the scope of the present invention, the follo~,ving propor-tions by weight of the most important cornponents of the light-sensitive composition are preferred, the percentages stated being by weight and based upon the total solids content, i.e. the total copying composition.
Polyurethane prepolymer: 30 to 80 per cent, with a residual iso-cyanate content of from 1 to 30 per cent, preferably from 5 to 25 per cent, most advantageously between 7 and 20 per cent.
Alkyd resin: 1 to 80 per cent, preferably 2 to 50 per cent.
Negative-working diazo compound: 20 to 70 per cent.
Stabilizer: 1 to 10 per cent.
Dyestuff or pigment: 0.5 to 5 per cent.
Contrast promoter (dyestuff): 0.1 to 1 per cent.
Homogeneous, aqueous acid solutions with a pH of not more than 3, to which up to 4 per cent of benzyl alcohol are added, are used as developers. The developer further contains neutral sodium and/or magnesium salts and wetting agents. The salt proportion should not exceed 3 per cent.
For commercial purposes, the light-sensitive copying composi-tions according to the present inventlon may be marketed in the form of a solution or dispersion, e.g. as a so-called resist, which is applied by the customer to an individual support, as is customary, e.g., for chemical milling, for the production of printed circuits or stencils, of name plates, screen printing forms and the like, and is then dried, ex-posed, and imagewise developed. In this case, the components of the light-sensitive copying composition are dissolved in a suitable solvent.
Suitable solvents are alcohols, ketones, esters, ethers and the like.
The partial ethers of glycols or of keto-alcohols were found to be of particular advant~ e.
K - 2 ~ 8 7 Z
Alternatively, the light-sensitive copying coMposition ac:cord-ing to the invention may be rnarketed in the form of a solid light-sensitive layer on a support, which is used for the preparation of printing forms, relief images, etch resists, stencils, mats, screen printing forms, in-dividual copies, and the like. A particularly important application is their use as storable, pre-sensitized printing plates for planographic printing .
The base material is coated with the copying composit~on from appropriate organic solvents or solvent mixtures, by casting, spraying, or immersion.
Suitable base materials are, e.g., plates of magnesium, zinc, copper, mechanically, chemically, and electrochemically roughened aluminum, anodized aluminum, or steel, but also polyester or acetate films, Perlon gauze etc., and the surfaces of these materials may be subjected to a pretreatment, if necessary. The base material may serve as the final support, or it may be an intermediate support from which the light-sensitive copying composition may be transferred, by lamination, onto the material to be processed.
The recording material produced from the copying compositions according to the invention may be used, on the one hand, for the pro-duction of images on suitable supports or receiving sheets, and, on the other hand, for the preparation of reliefs which may be used as printing forms, screens, resists, and the like. Moreover, it is pos-sible to use the light-sensitive copying compositions according to the invcntion for the preparation of UV-hardening printing inks or of UV-hardening lacquers which may be used for surface protection.
Most advantageously, the copying compositions according to the invention are used for the preparation o~ planographic printing ~ ~r~ J~
l~l;Z'~Z
forms, aluminum, especially anodized aluminum, being preEe~red as the base m~terial.
The printing forms, screens, resists, and the like are prepared in the customary manner from the appropriate recording materials, e.g.
after exposure under a suitable original, the non-image areas of the layer, which have retained their solubility, are removed by treatment with suitable developers, e.g. aqueous acid solutions.
By using the copying composition according to the present in-vention, a disadvantage of U. S. Patent No. 3,660,097, is overcome, viz. that polyurethane prepolymers containing free terminal isocyanate groups are not storable and thus are unsuitable for the preparation of copying compositions.
In German Offenlegungsschrift No. 2 ,361,931, it is expressly stated that the polyurethanes to be used must be prepared by a com-plete reaction of the isocyanate groups contained in the starting mater-ials .
Thus, it was the more surprising that copying compositions of the type proposed by the present invention, which contain free isocya-nate groups, can be stored under extremely adverse conditions and, in addition thereto, have the following advantages:
They are distinguished by a high practical light-sensitivity, good differentiation between image areas and non-image areas, high resolution, easy, scum-free development involving no environmental hazards, long printing runs, and good co npatibility of the components of the layer in the solvents selected for coating, e.g. ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, diacetone alcohol, and mixtures of these solvents with butyl acetate, ethylene ~Iycol methyl ether acctate, and methyl isobutyl ketone.
1~1.;2~7~gZ K-2487 The invention will he further illustrated by the following e:cam-ples. In these examples, the relation between parts by weight and parts by volume corresponc~s to that between grams and milliliters.
Percentages and proportions are by weight unless otherwise stated.
Example 1 A coating solution is prepared from 31.0 p.b.w. of a branched polyurethane prepolymer con-taining i7.0 per cent of terminal free NCO groups and obtained by the reaction of about 8 moles of 2,4-toluylene diisocyanate with 1 mole of butane diol-(1,4), 1 mole of polypropylene glycol (MG 1000), and 2 moles of 1 ,1 ,1-trimethylol-propane, 20.2 p.b.w. of an alkyd resin obtained by polycondensation of 40 p.b.w. of phthalic acid anhydride, 10 p.b.w. of glycerol, 20 p.b.w. of pentaerythritol, and 44 p.b.w.
of a branched, saturated monocarboxylic acid, with azeotropic distillation of the water produced, 31.2 p.b.w. of a tanning diazo, e.g. that obtained from paraformaldehyde and dip7nenyl-amine-4-diazonium-chloride or 3-methoxy-diphenylamine-4-diazonium-chloride with the addition of 85% phosphoric acid (see German Auslegeschrift No . 1, 21 4, 0 86, Example s 1 and 6), 3.2 p.b.w. of a red dyestuff oE the following structure O N- ~ -N=N- ~ -N/
H2-CH20H, 0.8 p.b.w. of Metanil Yellow (C.I. 13065), and 1~700.0 p.b.w. of ethylene glycol monomethyl ether.
2~1~7 The resulting light-sen~itive solution was coate(l as a layer weighing 1.1 g/m2 onto an anodi~ed aluminum support which had been pretreated as described in Example 7 of German Patent No. 1,160,733.
For this purpose, the anodized aluminum plate is immersed at about 70 to 90C in a 0.1 per cent by weight solution of polyvinyl phosphonic acid, rinsed with water, dried, and finally coated with the light-sensitive solution.
For the preparation of a lithographic printing plate, the follow-ing procedure is used:
The copying layer is exposed under a negative original, e.g.
for 65 seconds to a metal halide lamp of ~essrs. Brilliant, Type H-KOPS, 5kW output, at a distance of 130 cm. By means of a plush pad, the exposed layer is treated with a developer solution to remove the non-image areas, then rinsed with water, and squeegeed.
Upon determining the quality of the developed sample, it was found that step 5 of a step wedge is still fully blackened. The step wedge used is a silver halide film continuous tone step wedge with a density range from 0.05 to 3.05 and density increments of 0.15.
If a wet-brushed and pretreated aluminum support is whirler-coated with this composition, a layer of the same thickness requires an exposure time of 60 seconds for step 5 of the step wedge to be fully blackened .
A developer of the following composition may be used, and the same developer also may be used in the following examples:
25.0 p.b. vol. of completely desalted water, 0 . 75 p .b.w. of a wetting agent of the type of moclified ammonium alkyl sulfate ("Sanclopan FL"), 0.25p.b.w. of 8~% phosphoric acid, 0.~10p.b.w. of tartaric acid, ~rO~ K
Z
0.75p.b.w. of benzyl alcohol, and 0.50p.b.w. of Na2SO4 1() H2O.
Example 2 A coating solution is prepared from 31.2 p.b.w. oE the polyurethane prepolymer described in Example 1, 31.2 p.b.w. of a mixed diazo condensate produced as follows: 32.3 p.b.w. of 3-methoxy-diphenylamine-4-diazonium sulfate are dissolved in 170 p.b.w. of 85% phosphoric acid, 25.8 p.b.w. of 4,4'-bis-methoxy-diphenylether are dropwise added, and the mass is condensed for 5 hours at 40C. After dilut-ing with 250 p.b.w. of water, the chloride of the condensation product is precipitated by adding 220 p.b.v. of semi-concentrated hydrochloric acid. The chloride of the condensate is again dissolved in water and, after adding the sodium salt of mesitylene sul-fonic acid, the mesitylene sulfonate of the diazo compound is obtained in the form of a sparingly soluble 2 0 precipitate .
4.0 p.b.w. of one of the acids mentioned below, in ethylene glycol monomethyl ether.
Suitable acids are 85% phosphoric acid, 96% sul~uric acid, con-centrated perchloric acid, boric acid, and p-toluene sulfonic acid.
The solutions thus produced are applied to an anodized alumi-num support pretreated with polyvinyl phosphonic acid as in Example l, so that dry laycrs weighing 1.0 g/m each are produced.
Further processing is as described in Example 1.
K ~ a 7 ~.1;2Q9Z
The resulting printing forms are used for printing at least 50,000 copies Gn a Heidelberg offset printlng machine, type KOR.
Example 3 The following components 29.0 p.b.w. of the polyurethane prepolymer used in Example 1, 29.0 p.b.w. of an alkyd resin obtained by the polyconden-sation of 40 p.b.w. of phthalic acid anhydride, 30 p.b.w. of a mixture of glycerol and pentaerythritol, and 38 p.b.w. of a branched saturated monocarboxylic acid, with azeotropic distillation of the water produced, 30.0 p.b.w. of the mixed diazo cQndensate used in Example 2, 4.0 p.b.w. of 85% phosphoric acid, 3.0 p.b.w. of a blue dyestuff produced by condensation of 2,4-dinitro-6-chloro-benzene-diazonium salt with 2-methoxy-5 -acetylamino-N-cyanoethyl-4-hydroxy-ethylaniline, and 1.0 p.b.w. of MetanilYellow (C.I. 13065), are dissolved in ethylene glycol monomethyl ether and the solution is filtered .
The solution thus prepared is designated as "Solution a". An aluminum support which had been mechanically roughened by wet-brushing and whose surface had been pretreated with polyvinyl phos-phonic acid as described in Example 1 is coated with "Solution a"
above and the solvent is then removed by drying.
The resulting copyiny layer is exposed and developed as des-cribed in Example 1.
Complete developrnent takes 90 seconds.
A sample of the same material which had been placed in a con-ditioning cabinet, at a temperature of 42 C and an atmospheric moisture Q~2 K-2487 of 62%, may be satisfactorily developed within 90 seconds even after a rcsidence time in the conditioning cabinet of 182 days.
In a comparison test, a coating solution "b" is prepared which contains the same components as "Solution a" with the exception of the phosphoric acid component.
The above described support is coated with "Solution b" and the resulting copying layer is processed as in Example 1.
When processing "Sample b", it is observed that only a freshly prepared sample can be satisfactorily developed within 90 seconds.
Even after a storage of only one day at room temperature (25 C), it is no longer possible to develop the unstabilized copying layer without scumming.
Ageing of the copying layer increases as time progresses. After 7 days, it is no longer possible to produce a differentiation between the image areas and the non~image areas, even if the developing time is prolonged to 5 times its original length.
Example 4 A solution with a solids content of 7.5 per cent is produced from the following components:
31.0 p.b.w. of the polyurethane prepolymer used in Example 1, 62.4 p.b.w. of the mixed diazo condensate described in Example 2, 3.0 p.b.w. of 85% phosphoric acid, and 3.0 p.b.w. of Crystal Violet and ethyleneglycol monomethyl ether.
The solution is applied, as a layer weighing 1.5 g/m2, to an eloxated aluminum support (weight of the oxide layer: 2 g/m ), pre-treated with polyvinyl phosphonic acid as describecl in Example 1.
-- 2~ --Z K - 2 fi 8 7 By exposing the material for 80 seconds under a negative ori~
nal, using the metal halide lamp described in l~arnple 1 at a distance of 130 cm, and developing it for 90 seconds with the developer of Ex-ample 1, flawless copies are obtained. With an exposure time of 80 seconds, the step wedge is fully blackened up to step 5.
After development, the printing plate shows excellent contrast, so that even the finest film edges are clearly discernible.
A plate processed in this manner yields 110,000 copies on a printing machine.
Example 5 A light-sensitive copying composition is prepared from the fol-lowing components:
61.0 p.b.w. of a branched polyurethane prepolymer which contains 16 per cent of terminal free NCO groups and is obtained by reacting 4,4'-diphenylmethane-diiso-cyanate with a mixture of butane diol-(1,4), polypro-pylene glycol, and 1,1,1-trimethylol propane, 31.2 p.b.w. of the mixed diazo condensate described in Example 2, 4.0 p.b.w. of 85% phosphoric acid, 4 .0 p .b.w. of the red dyestuff used in Example 1, and 1.0 p.b.w. of Methyl Orange (C.I. 13025), dissolved in ethyleneglycol monomethyl ether.
If the layer has a thickness corresponding to a weight of 1.4 g/m and the above mentioned red dyestuff is used, an exposure time of 50 sec. (metal halide lamp) at a distance of 130 cm is required to cause step 5 of the copy of the step wedge to be fully blackened.
~fter d~velopment, the plate shows a brilliant, deeply violet contra st .
Exam~l~ 6 ~, The following components 60.0 p.b.w. of a polyurethane prepolymer with an iso-cyanate content of about 20 per cent, based on the molecular weight of ihe prepolymer, and correspond-ing to the following formula NCO
CH2-O-CO-NH- ~-CH3 / NCO
H3C-CH2-C/ CH2-O-CO-NH- ~-C~I3 NCO
\CH2-O-CO-NH- ~-CH3 30.0 p.b.w. of the mixed condensate used in Example 2, 7.5 p.b.w. of Rhodamine 6 GDN extra (C.I. 45160), and 3.3 p.b.w. of 85% phosphoric acid were applied, as a S per cent solution in ethyleneglycol monomethyl ether, onto an anodized support, so that the resulting layer weighed 1.0 ~/m2. After 30 seconds' exposure to a metal halide lamp at a dis-tance of 130 cm and development with the developer used in Example 1, a run of 70,000 copies could be printed.
The layer shows an exceptionally steep gradation corresponding to only one half tone step of the step wed~e.
Example 7 33 .0 p .b.w. of the polyurethane prepolymer described in Example 1, 25.0 p.b.w. of the alkyd resin used in Example 3, 3.4 p.b.w. of polyvinyl formal, 35.2 p.D.W. of the mixed diazo condensate described in Example 2, K- 2 1 ~ 7 3.0 p.b.w. of 85% phosphoric acid, 3.0 p.b.w. of Rhodamine 6 GDN extra (C.I, 45160), and 0.8 p.b.w. of Metanil Yellow (C.I. 13065) are dissolved in 2000.0 p.b.w. of ethyleneglycol monomethyl ether.
A layer weighing 1.0 g/m2 is applied to wet-brushed aluminum which had been treated with polyvinyl phosphonic acid as described in Example 1. After 45 seconds' exposure under a negative original to the light of a metal halide lamp at a distance of 130 cm, the layer is de-veloped for 45 seconds with the developer used in Example 1. Excel-lent copies are produced which yield 35,000 prints in a printing machine .
Even after three months' storage, the properties of the copying layer are unchanged.
Example 8 A 5% solution in ethyleneglycol monomethyl ether is prepared from the following components:
30.0 p.b.w. of the polyurethane prepolymer described in Example 1, 28.0 p.b.w. of the allcyd resin described in Example 3, 30.0 p.b.w. of the mixed diazo condensate described in Example 2, 4.0 p.b.w. of 85% phosphoric acid, 3.0 p.b.w. of a pigment dispersion composed of 10 per cent by weight of "llostaperm Blue B G" (C.I.
74160) and 10 per cent by weight of polyvinyl formal and 80 per cent by weight of cthylene glycol methyl ether acetate, and 1.0 p.b.w. of Metallil Yellow (C.I. 13065), - 27 - .
2 K - 2 ~ 3 7 and the solution is whirler-coated onto an eloxated aluminum support which had been pretreated with polyvinyl phosphonic acid as described in Example 1, to produce a layer weighing 1~2 g/m .
After 30 seconds' exposure to a metal halide lamp from a dis-tance of 130 cm, the layer may be developed within 90 seconds with the developer mentioned in Example 1.
The copies thus produced have a good contrast which does not noticeably diminish even after five times the developing time.
Printing runs of 130,000 copies were printed on a printing ma-chine. The properties of the copying layer are still good after 50 days' storage at a temperature of 42 C and a humidity of 62%.
Example 9 61.0 p.b,w. of the polyurethane prepolymer described in Example 1, 31.2 p.b.w. of the condensation product of an aromatic diazonium compound used in Example 2, 4.0 p.b.w. of ~5% phosphoric acid, 4.0 p.b.w. of Rhodamine 6 GDN extra (C.I. 45160), and 1.0 p.b.w. of MetanilYellow (C.I. 13065) are dissolved in ethyleneglycol monomethyl ether.
This solution is then coated onto a support of electrochemically roughened and anodized aluminum with an oxide layer of 3 g/m2, which had been pretreated with polyvinyl phosphonic acid as described in Example 1.
The dry weight of the layer is between 1.0 and 1.4 g/m2. For the preparation of a lithographic printing plat'e, the following procedure is employed:
The negative-wor~ing reproduction layer is exposed for ~0 sec-onds under a necJative original to the light of a metal halide lamp at a -- 2~3 --distance of 130 cm and is then treated with the developer used in Exam-ple 1.
From the resultiny printing form, a run of more than 100,000 flawless prints may be printed on a printing machine.
Example 10 A coating solution is prepared from 30. 0 p .b.w. of the polyurethane prepolymer described in Example 1, 60.0 p.b.w. of the mixed diazo condensate described in Example 2, .0 p.b.w. of 85% phosphoric acid, and 2.0 p.b.w. of the red dyestuff used in Example 1, dissolved in ethylene glycol monomethyl ether, and the resulting solution is applied to a 50~m thick, biaxially stretched polyethylene terephthalate film in such a manner that the applied layer weighs 3.5 g/m2 The coated film is exposed for 3 minutes under a negative origi-nal, using an exposure device (8 kW Xenokop apparatus of Messrs .
Klimsch ~ Co.) at a distance of 75 cm, and is then developed for 90 seconds with the developer used in Example 1. An excellent copy is produced .
If four solutions prepared from the polyurethane prepolymer men-tioned in Example 1, a mixed diazo condensate, and phosphoric acid are dyed in the four primary colors yellow, red, blue, and black, and the four solutions are then used for coating polyester films, color proofing foils are obtained which may be used for a negative-working color proofin~ system according to the overlay principle.
For this purpose, the individual color proofing films are exposed under the corresponding silver halide color separations, developed with ~ Tr~ rK
the cleveloper of Example 1, and the resulting color ima~es are careflllly dried. If the resulting four images are superimposed in register with each other, a four-colored image corresponding to the original is pro-duced .
Example 1 1 A coating solution is prepared from the following components:
28.8 p.b.w. of the polyurethane prepolymer described in Example 1, 25 . 0 p .b .w . of the alkyd resin described in Example 3, 3.0 p.b.w. of polyvinyl formal, 30.0 p.b.w. of the mixed diazo condensate described in Example 2, 4.0 p.b.w. of 85% phosphoric acid, in 92.0 p.b.w. of ethyleneglycol monomethyl ether, and 46.C p.b.w. of ethyleneglycol methyl ether acetate.
The resulting solution is applied as a layer weighing 1.4 g/m2 to a polyethylene terephthalate film which had been hydrophilized by a silica treatment according to German Au s lege schrift No . 1, 2 2 8, 414 .
For this hydrophilizing treatment, the surface of the film is treated with a mixture comprising 1) an aqueous solution of dichloro acetic acid or trichloro acetic acid or 2,2,3-trichloro propionic acid, 2) very finely divided pyrogenic silica obtained in the gaseous phase, and 3) a con-ventional wetting agent which is resistant to the action of acids and heat, and is then dried. After exposure (45 seconds at a distance of 75 cm, using a Xenokop apparatus of 8 kW) and development as in Ex-ample 1, flawlcss copies result. Treatment with an image intensifier may be combined with the application o~ a preserving sohltion.
Examplc 12 30.0 p.b.w. of the polyurcthane prepolymer described in Example 1, 60.0 p.b.w. of the mixed diazo condensate described in Example 2, 4.0 p.b.w. of 85/~, phosphoric acid, and 4.0 p.b.w. of the red dyestuff used in Example 1, are dissolved in 900 p.b.w. of ethyleneglycol monomethyl ether and applied, as a layer weighing 3 g/m, to a zinc plate cleaned by means of a 0.3 per cent nitric acid solution. The plate is then exposed for 3 minutes, at a distance of 75 cm, to an 8 kW xenon lamp under a nega-tive original, developed with the developer used in Example 1, and finally etched with 7.5% nitric acid. The hardened image areas form an excellent etch resist.
Example 13 34.5 p.b.w. of the polyurethane prepolymer described in Example 1, 11.5 p.b.w. of a mixed diazo condensate prepared from a solution of 32.3 g of 3-methoxy-diphenyl-amine-4-diazonium sulfate in 100 ml of 86% phosphoric acid to which 25 . 8 g of 4 ,4'-bis-methoxymethyl-diphenyl ether are dropwise added. After 17 hours' condensation at ~0C, the methane sulfonate was separated, purified and dried. This method of preparation is described in Example 4 of German Offenlegungsschrift No . 2, 041, 395;
2.4 p.b.w. of 85% phosphoric acid, 1.6 p.b.w. of Crystal Violet tc~I~ 42555), in 900.0 p.b.w. of ethyleneglycol monomethyl ether.
The solution is applied, as a layerweighing 1.0 g/m, to an anodi7ed aluminum support corresponding to the one used in Example 1.
Z
The copying layer is exposed for 25 seconds under 2 negative original to the metal halide lamp described in Example 1 (clistance: 130 cm) ancl then developed with the cleveloper used in Example 1.
The plate thus obtained shows good contrast and is ready for printing .
It will be obvious to those skilled in the art that many modifica-tions may be made within the scope of the present invention without departing from the spirit thereof, and the invention includes all such modifications .
Preferably employed are 4-amino-diphenylamine and 3-methyl-4-amino-diphenylamine, particularly preferably are the 3-alkoxy-4-amino-diphenylamines having 1 to 3 carbon atoms in the alkoxy group, especi-ally the 3-methoxy-4-amino-diphenylamine.
Components B
Similarly, a plurality of compounds are suitable as components B
K~2'1 87 in the pr~paration of the mixed condensates. An important class are the substituted or unsubstituted aromatic hyclrocarbons and aromatic hetero-cyclic compounds.
Examples of unsubstituted aromatic isocyclic and heterocyclic compounds which may be used as components B are, e.g., benzene, naphthalene, anthracene, phenanthrene, pyrene, indene, fluorene, acenaphthene, thiophene, furan, benzofuran, diphenylene oxide, benzo-thiophene, acridine, carbazole, phenothiazine, and others which may be substituted by one of the following groups:
-N (R8) 2 wherein R7 may be H, -CO-alkyl, -CO-aryl, -CO-heteroyl, -CO-aralkyl, -S02-alkyl, -S02-aryl, -S02-aralkyl, -S02-heteroyl, -CONH2, -CSNH2, -CONH-alkyl, -CONH-aryl, -CO-O-alkyl, -CO-O-aryl, -CS-O-aryl, and-CS-O-alkyl, and R8 may be H, an alkyl, aryl, or an aralkyl group.
The meanings of certain terms are as follows:
Alkyl: A branched or unbranched alkyl group with 1 to 10 carbon atoms which may be substituted, e.g. by -halo~en, -alkoxy, -OH, -COOH, -CONH2, -CN, -CO-CH3, -S03H, or -P03H2, or hyclro~ens in nei~hborin~ positions may be replaced by oxy~en (epcxides) or _ g _ K-~4~7 r~moved (multiple bonds). The alkyl radic~l also may be interrupted, e . g . by -O , -S-, -N (alkyl)-, -SO2-, or -SO- .
Aryl: A mono- or polynuclear aromatic ring which, includiny alkyl, alkoxy, or aralkyl ~roups which may be linked thereto, contains from 6 to 20 carbon atoms. The aryl nucleus may carry additional sub-stituents .
Aralkyl: A group containing 7 to 20 carbon atoms which is com-posed of alkyl and aryl radicals (corresponding to the above definition).
Alkoxy: O-alkyl group, the alkyl having the above meaning.
The alkyl, aryl, aralkyl, and alkoxy groups may be present one or more times, either alone or together.
According to the above, the compounds to be employed as com-ponents B or components Bl derived therefrom belong to the following groups of substances; for example:
aromatic compounds (iso- and heterocyclic), unsubstituted aromatic amines phenols and thiophenols phenol ethers and thiophenol ethers aromatic compounds substituted by alkyl, aralkyl or aryl groups urea, thiourea, carboxylic acid amides (aliphatic and aromatic), and sulfonie acid amides (aliphatie and aromatie).
In order to limit the eontribution of these substances to the molecular weight of B, the proportion of the four above-mentioned sub-stituents in the structure of the molecule of compound B is limited, the primary aromatic iso- or heterocyclic ring or the condensed ring system being substituted only to such an extent that the aromatic compound is increased, in the case of substitution by alkyl groups: by not more than 10 carbon atoms, by aryl groups: by not more than 20 carbon atoms, ~--2!-~37 g2 by aralkyl groups: by not more than 20 carbon atoms, and by alkoxy groups: by not more than 10 carbon atoms.
The total increase in C atoms by these four types of substituents should not exceed 30 C atoms with respect to the original aromatic nucleus .
Generally, components B are preferred which have a molecular weight of less than 500, preferably less than 250, amines being calcu-lated as free amines, not in the salt form, and acid groups being calcu-lated in the H-form. If the compounds are aromatic compounds, those compounds are preferred within these limits which contain not more than 4, preferably not more than 1 to 2, most advantageously 2, individual aromatic rings (fused to each other and/or connected with each other, preferably by homopolar bonds and/or intermediate members).
This means that the number of substituents with longer chains, i.e. those having a relatively large number of C atoms, which may be present at the same time, is smaller than the number of substituents with fewer C àtoms. C~enerally, the short-chain alkyl and alkoxy groups tl to 4 carbon atoms) and the smaller aromatic radicals in aryl and aral-kyl groups (up to 12 carbon atoms) are preferred, because the corre-sponding compounds are more easily soluble in the condensation media and condensation thus can be performed more easily. For the same reason, substitution is limited as described above.
The condensable iso- or heterocyclic aromatic rings also may have substituents exerting a deactivating effect on the nuclei, e.g.
O2N-, HOOC-, NC-, HO3S, and H2O3P ~roups, provided these groups do not destroy the condensability of these rings. This means that such substituents may be particularly introduced if the ring as SUCIl is easily condensable or carries substituents having a strongly activating cffect.
Another possibility for introducing deactivatin~ substituents without Z
unduly reducing the condensability of the ring is to place the substitu-ents in side chains, e.g. aliphatic side chains.
Substituents deactivating nuclear condensation also may be present in those cases in which the reactivity of the condensable nuc-leus is not necessary, because the nucleus has substituents at which condensation can take place. Such substituents are listed above and include, for example, the groups -CO-NH2, -SO2NH2, and -SO2NH-alkyl .
Of the classes of compounds indicated, from which the compounds B and Bl derive, generally those are preferred which are unsaponsifiable or only difficultly saponifiable under acid condensation conditions. The same applies to the diazo compounds A(-D) .
For this reason, those compounds B or 81 of the series of aro-matic iso- and heterocyclic compounds are advantageous which are either unsubstituted or carry alkyl, aralkyl, aryl, alkoxy, alkylmercapto, aryloxy, arylmercapto, OH, SO, and amino groups as substituents, if desired, in addition to unsaponifiable deactivating substituents, e.g.
COOh. Of these compounds, those aromatic iso- and heterocyclic compounds are particularly preferred which are unsubstituted or contain, as substituents, one or more alkyl, aralkyl, aryl, alkoxy, alkylmercap-to, arylmercapto, and aryloxy groups, particularly when condensates are desired which should not contain salt-forming ~roups other than the . .
diazo group.
Exemplary of particularly suitable compounds B or ~1 are those which are derived from diphenyl ether, diphenyl sulfide, diphenyl methane, or diphenyl, and may contain one or two substituents selected from halogen atoms, alkyl ~roups, and allcoxy ~roups, but are prefer-ably unsubstituted.
If thesc compounds arc condensed with diphenylamirle-~-diazonium salts which are unsubstit~ltcd or substituted by a lower a,kyl , 1~12~g2 group or a lo~ver alkoxy group containing up to 3 carbon atoms, mixed condensates are obtained which can be readily precipitated and in good yields in the form oE the salts of hyclrochloric acid, hydrobromic acid, or of suitable sulfonic acids, especially when the component B or B1 is employed in a proportion from 0.5 to 2 moles per mole of diazo compound.
The new condensation products of the invention generally contain 0.1 to 50 moles, preferably 0.1 to 20 moles, on the average, of units of component B per mole of units of component A(-D)n. A particularly pre-ferred range is from 0.2 to 2 moles of B per mole of A(-D) .
The mixed diazo condensates known fromGerm~n Offenlegungs-schrift No. 2 ,041,395, i.e. condensation products in which the anion of the diazonium salt is derived from an aliphatic monosulfonic acid with 1 to 6 carbon atoms, are particularly suitable for the copying composition according to the present invention.
The aliphatic monosulfonic acids forming the anion of the diazon-ium condensates used according to the invention normally have bet~veen 1 and 6 carbon atoms and may be substituted, if desired, by substitu-ents which are not too heavy, e.g. halogen atoms, viz. fluorine, chlorine, bromine or iodine, hydroxy groups, ether groups, and the like.
Normally, not more than 1 substituent is present. The aliphatic chain may be straight, branched, or annular and may also contain double bonds.
Methane sulfonates are particularly preferred.
The polyurethane prepolymers with free terminal isocyanate groups used according to the present invention normally are composed of three components, viz. a diisocyanate (I), a polyol ~vith at least three free OH groups (II), and a diol (III).
Suitable diisocyanates (I) are: 2,4-toluylene diisocyanate, 2,6-toluylene diisocyanate, 4,4'-diphenylmethane diisocyanate, isophoron-diisocyanate, 2 ,2 ,4-trimethyl-hexamethylene diisocyanate, hexamethyl-Qg2 elle cliisocyanate, xylylene diisocyanate, 3,3'-bitoluylene-4,~'-di-isocyanate, 3, 3 ' -dimethyl-cyclohexane-4, 4 ' -diisocyanate, ~, 4 '-pheny l-cyclohexylmetha ne-dii socya nate, 4, 4 ' -dicyclohexyl metha ne -diisocyanate, phenylene-diisocyanate, 4,4'-diphenylether-diisocya-nate, naphthalene-diisocyanate, and Iysine-diisocyanate.
2, 4-Toluylene-dii socyanate, 2, 6-toluyl e ne-diisocya nate, 4, 4 ' -diphenylmethane-diisocyanate, and 2,2,4-trimethyl-hexamethylene-diisocyanate are preferred.
The diisocyanates may be used either alone or in admixturb with each other.
Suitable polyols (II) are, e.g.: 1 ,1,l-trimethylol propane, 1 ,1 ,1-trimethylol ethane, pentaerythritol, dipentaerythritol, and others .
Diols (III) which may be used are, among others, polyalkylene glycols of the following general formula HO(-CHR-CH2-O)n-H
-whereln R stands for H or all~yl, preferably for H or methyl, and n is an integer from 1 to 10, or compounds of the following general formula 2 0 HO-CnH 2 n~OH
wherein n is an integer from 2 to 10.
As a rule, the diisocyanates are reacted in known manner with a deficiency of polyol and diol, so that the proportion of free terminal isocyanate groups in the resulting polyurethane is in the range from 1 to 30 per cent by weight, preferably from 5 to 25 per cent by weight, and most advantageously between 7 and 20 per cent by weight.
Depencliny upon the type and proportion of the polyol component, the polyurethane prepolynlers thus prepared are more or less branched.
.
~-24~7 For stabilization of the copying composition, a eompound ~,vit~
acid character must be added thereto. Suitable acids are mineral acids and also strong organic acids, phosphoric acid, sulfuric acid, perchlor-ic acid, boric acid, and p-toluene sulfonic acid being preferred. Phos-phoric acid is a particularly advantageous acid.
For fine adjustment of the layer properties, a non-drying syn-thetic alkyd resin with a branched, saturated fatty acid component (cf.
Karsten "Lackrohstofftabellen", page 73 et seq.) is added to the copy-ing composition, by which the impact strength of the polyurethane pre-polymer is increased and longer runs become possible, if the copying eomposition is used as a printing image. At the same time, the resin exerts a plasticizing effect on the prepolymer.
Preferred alkyd resins are those which are obtained by polycon-densation of phthalic acid anhydride, polyols, e.g. glycerol, pentaeryth-ritol, 1 ,1 ,1-trimethylol propane, or 1 ,1 ,1-trimethylol ethare, and a branched monocarboxylic acid, e.g. i-nonane acid, i-octane acid, etc.
Further, knownplasticizers, adhesionpromoters, dyestuffs, pigments, eolor couplers, and/or UV absorbers may be added to the eopying compositions of the invention.
The type and quantity of such additives depend on the purpose for which the copying composition according to the invention is des-tined. In any ease, however, care must be taken that the substances added do not absorb an excessive proportion of the actinic light requircd for eross-linking and thus reduce the practical licJht-sensitivity of the eomposition .
Suitable plasticizers are, e.g.: dibutyl phthalate, diisooctyl-adipate, nitro esters, alkyl and aryl phosphate esters, chlorinated paraffins, and glycols or aliphatic polyols.
If it is desired to ensure good storability at relative high atmos-pheric moisture, water-insoluble plasticizers are preferred.
Adhesion promoters are added in those cases where the light-sensitive copying compositions according to the invention are to be ex-posed to p~rticular stress, e.g. when they are to be used as photore-sist materials. Suitable adhesion promoters are, e.g., monomeric or polymeric organic silanes, nitrogen-containing heterocyclic compounds, such as those disclosed in U. S. Patents Nos. 3,645,722, 3,622,234, and 3,827,908, heterocyclic mercaptan compounds according to German Offenlegungsschrift No. 2,028,733, mercapto alkanoic acid anilides according to German Offenlegungsschrift No. 2,448,821, and mercapto alkanoic acid esters according to German Offenlegungsschrift No.
2,448,750.
Further, the light-sensitive copying compositions according to the invention may contain dyestuffs and/or pigments, which may serve to increase the contrast and also to harden the layer. Suitable dye-stuffs are mentioned, e.g., in U. S. Patents Nos. 3,218,167, and 3,884,693.
Rhodamine 6 GND extra (C.I. 45160), Crystal Violet (C.I. 42555), and a blue dyestuff obtained by condensation of 2,4-dinitro-6-chloro-benzene diazonium salt with 2-methoxy-5-acetyl-amino-N-cyanoethyl-N-hydroxy ethyl aniline, are particularly suitable.
MetanilYellow (C.I. 13065) and Methyl Oran~e (C.I. 13025) may be used to increase the image contrast after development.
Further, the copying compositions according to the invention may contain UV-absorbers which serve as anti-halation filters. Suit-able, non-coloring substances are described, e.g., in German Of Een-legungsschrift No . 2,243, J 82.
~?~Z K~24~7 Within the scope of the present invention, the follo~,ving propor-tions by weight of the most important cornponents of the light-sensitive composition are preferred, the percentages stated being by weight and based upon the total solids content, i.e. the total copying composition.
Polyurethane prepolymer: 30 to 80 per cent, with a residual iso-cyanate content of from 1 to 30 per cent, preferably from 5 to 25 per cent, most advantageously between 7 and 20 per cent.
Alkyd resin: 1 to 80 per cent, preferably 2 to 50 per cent.
Negative-working diazo compound: 20 to 70 per cent.
Stabilizer: 1 to 10 per cent.
Dyestuff or pigment: 0.5 to 5 per cent.
Contrast promoter (dyestuff): 0.1 to 1 per cent.
Homogeneous, aqueous acid solutions with a pH of not more than 3, to which up to 4 per cent of benzyl alcohol are added, are used as developers. The developer further contains neutral sodium and/or magnesium salts and wetting agents. The salt proportion should not exceed 3 per cent.
For commercial purposes, the light-sensitive copying composi-tions according to the present inventlon may be marketed in the form of a solution or dispersion, e.g. as a so-called resist, which is applied by the customer to an individual support, as is customary, e.g., for chemical milling, for the production of printed circuits or stencils, of name plates, screen printing forms and the like, and is then dried, ex-posed, and imagewise developed. In this case, the components of the light-sensitive copying composition are dissolved in a suitable solvent.
Suitable solvents are alcohols, ketones, esters, ethers and the like.
The partial ethers of glycols or of keto-alcohols were found to be of particular advant~ e.
K - 2 ~ 8 7 Z
Alternatively, the light-sensitive copying coMposition ac:cord-ing to the invention may be rnarketed in the form of a solid light-sensitive layer on a support, which is used for the preparation of printing forms, relief images, etch resists, stencils, mats, screen printing forms, in-dividual copies, and the like. A particularly important application is their use as storable, pre-sensitized printing plates for planographic printing .
The base material is coated with the copying composit~on from appropriate organic solvents or solvent mixtures, by casting, spraying, or immersion.
Suitable base materials are, e.g., plates of magnesium, zinc, copper, mechanically, chemically, and electrochemically roughened aluminum, anodized aluminum, or steel, but also polyester or acetate films, Perlon gauze etc., and the surfaces of these materials may be subjected to a pretreatment, if necessary. The base material may serve as the final support, or it may be an intermediate support from which the light-sensitive copying composition may be transferred, by lamination, onto the material to be processed.
The recording material produced from the copying compositions according to the invention may be used, on the one hand, for the pro-duction of images on suitable supports or receiving sheets, and, on the other hand, for the preparation of reliefs which may be used as printing forms, screens, resists, and the like. Moreover, it is pos-sible to use the light-sensitive copying compositions according to the invcntion for the preparation of UV-hardening printing inks or of UV-hardening lacquers which may be used for surface protection.
Most advantageously, the copying compositions according to the invention are used for the preparation o~ planographic printing ~ ~r~ J~
l~l;Z'~Z
forms, aluminum, especially anodized aluminum, being preEe~red as the base m~terial.
The printing forms, screens, resists, and the like are prepared in the customary manner from the appropriate recording materials, e.g.
after exposure under a suitable original, the non-image areas of the layer, which have retained their solubility, are removed by treatment with suitable developers, e.g. aqueous acid solutions.
By using the copying composition according to the present in-vention, a disadvantage of U. S. Patent No. 3,660,097, is overcome, viz. that polyurethane prepolymers containing free terminal isocyanate groups are not storable and thus are unsuitable for the preparation of copying compositions.
In German Offenlegungsschrift No. 2 ,361,931, it is expressly stated that the polyurethanes to be used must be prepared by a com-plete reaction of the isocyanate groups contained in the starting mater-ials .
Thus, it was the more surprising that copying compositions of the type proposed by the present invention, which contain free isocya-nate groups, can be stored under extremely adverse conditions and, in addition thereto, have the following advantages:
They are distinguished by a high practical light-sensitivity, good differentiation between image areas and non-image areas, high resolution, easy, scum-free development involving no environmental hazards, long printing runs, and good co npatibility of the components of the layer in the solvents selected for coating, e.g. ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, diacetone alcohol, and mixtures of these solvents with butyl acetate, ethylene ~Iycol methyl ether acctate, and methyl isobutyl ketone.
1~1.;2~7~gZ K-2487 The invention will he further illustrated by the following e:cam-ples. In these examples, the relation between parts by weight and parts by volume corresponc~s to that between grams and milliliters.
Percentages and proportions are by weight unless otherwise stated.
Example 1 A coating solution is prepared from 31.0 p.b.w. of a branched polyurethane prepolymer con-taining i7.0 per cent of terminal free NCO groups and obtained by the reaction of about 8 moles of 2,4-toluylene diisocyanate with 1 mole of butane diol-(1,4), 1 mole of polypropylene glycol (MG 1000), and 2 moles of 1 ,1 ,1-trimethylol-propane, 20.2 p.b.w. of an alkyd resin obtained by polycondensation of 40 p.b.w. of phthalic acid anhydride, 10 p.b.w. of glycerol, 20 p.b.w. of pentaerythritol, and 44 p.b.w.
of a branched, saturated monocarboxylic acid, with azeotropic distillation of the water produced, 31.2 p.b.w. of a tanning diazo, e.g. that obtained from paraformaldehyde and dip7nenyl-amine-4-diazonium-chloride or 3-methoxy-diphenylamine-4-diazonium-chloride with the addition of 85% phosphoric acid (see German Auslegeschrift No . 1, 21 4, 0 86, Example s 1 and 6), 3.2 p.b.w. of a red dyestuff oE the following structure O N- ~ -N=N- ~ -N/
H2-CH20H, 0.8 p.b.w. of Metanil Yellow (C.I. 13065), and 1~700.0 p.b.w. of ethylene glycol monomethyl ether.
2~1~7 The resulting light-sen~itive solution was coate(l as a layer weighing 1.1 g/m2 onto an anodi~ed aluminum support which had been pretreated as described in Example 7 of German Patent No. 1,160,733.
For this purpose, the anodized aluminum plate is immersed at about 70 to 90C in a 0.1 per cent by weight solution of polyvinyl phosphonic acid, rinsed with water, dried, and finally coated with the light-sensitive solution.
For the preparation of a lithographic printing plate, the follow-ing procedure is used:
The copying layer is exposed under a negative original, e.g.
for 65 seconds to a metal halide lamp of ~essrs. Brilliant, Type H-KOPS, 5kW output, at a distance of 130 cm. By means of a plush pad, the exposed layer is treated with a developer solution to remove the non-image areas, then rinsed with water, and squeegeed.
Upon determining the quality of the developed sample, it was found that step 5 of a step wedge is still fully blackened. The step wedge used is a silver halide film continuous tone step wedge with a density range from 0.05 to 3.05 and density increments of 0.15.
If a wet-brushed and pretreated aluminum support is whirler-coated with this composition, a layer of the same thickness requires an exposure time of 60 seconds for step 5 of the step wedge to be fully blackened .
A developer of the following composition may be used, and the same developer also may be used in the following examples:
25.0 p.b. vol. of completely desalted water, 0 . 75 p .b.w. of a wetting agent of the type of moclified ammonium alkyl sulfate ("Sanclopan FL"), 0.25p.b.w. of 8~% phosphoric acid, 0.~10p.b.w. of tartaric acid, ~rO~ K
Z
0.75p.b.w. of benzyl alcohol, and 0.50p.b.w. of Na2SO4 1() H2O.
Example 2 A coating solution is prepared from 31.2 p.b.w. oE the polyurethane prepolymer described in Example 1, 31.2 p.b.w. of a mixed diazo condensate produced as follows: 32.3 p.b.w. of 3-methoxy-diphenylamine-4-diazonium sulfate are dissolved in 170 p.b.w. of 85% phosphoric acid, 25.8 p.b.w. of 4,4'-bis-methoxy-diphenylether are dropwise added, and the mass is condensed for 5 hours at 40C. After dilut-ing with 250 p.b.w. of water, the chloride of the condensation product is precipitated by adding 220 p.b.v. of semi-concentrated hydrochloric acid. The chloride of the condensate is again dissolved in water and, after adding the sodium salt of mesitylene sul-fonic acid, the mesitylene sulfonate of the diazo compound is obtained in the form of a sparingly soluble 2 0 precipitate .
4.0 p.b.w. of one of the acids mentioned below, in ethylene glycol monomethyl ether.
Suitable acids are 85% phosphoric acid, 96% sul~uric acid, con-centrated perchloric acid, boric acid, and p-toluene sulfonic acid.
The solutions thus produced are applied to an anodized alumi-num support pretreated with polyvinyl phosphonic acid as in Example l, so that dry laycrs weighing 1.0 g/m each are produced.
Further processing is as described in Example 1.
K ~ a 7 ~.1;2Q9Z
The resulting printing forms are used for printing at least 50,000 copies Gn a Heidelberg offset printlng machine, type KOR.
Example 3 The following components 29.0 p.b.w. of the polyurethane prepolymer used in Example 1, 29.0 p.b.w. of an alkyd resin obtained by the polyconden-sation of 40 p.b.w. of phthalic acid anhydride, 30 p.b.w. of a mixture of glycerol and pentaerythritol, and 38 p.b.w. of a branched saturated monocarboxylic acid, with azeotropic distillation of the water produced, 30.0 p.b.w. of the mixed diazo cQndensate used in Example 2, 4.0 p.b.w. of 85% phosphoric acid, 3.0 p.b.w. of a blue dyestuff produced by condensation of 2,4-dinitro-6-chloro-benzene-diazonium salt with 2-methoxy-5 -acetylamino-N-cyanoethyl-4-hydroxy-ethylaniline, and 1.0 p.b.w. of MetanilYellow (C.I. 13065), are dissolved in ethylene glycol monomethyl ether and the solution is filtered .
The solution thus prepared is designated as "Solution a". An aluminum support which had been mechanically roughened by wet-brushing and whose surface had been pretreated with polyvinyl phos-phonic acid as described in Example 1 is coated with "Solution a"
above and the solvent is then removed by drying.
The resulting copyiny layer is exposed and developed as des-cribed in Example 1.
Complete developrnent takes 90 seconds.
A sample of the same material which had been placed in a con-ditioning cabinet, at a temperature of 42 C and an atmospheric moisture Q~2 K-2487 of 62%, may be satisfactorily developed within 90 seconds even after a rcsidence time in the conditioning cabinet of 182 days.
In a comparison test, a coating solution "b" is prepared which contains the same components as "Solution a" with the exception of the phosphoric acid component.
The above described support is coated with "Solution b" and the resulting copying layer is processed as in Example 1.
When processing "Sample b", it is observed that only a freshly prepared sample can be satisfactorily developed within 90 seconds.
Even after a storage of only one day at room temperature (25 C), it is no longer possible to develop the unstabilized copying layer without scumming.
Ageing of the copying layer increases as time progresses. After 7 days, it is no longer possible to produce a differentiation between the image areas and the non~image areas, even if the developing time is prolonged to 5 times its original length.
Example 4 A solution with a solids content of 7.5 per cent is produced from the following components:
31.0 p.b.w. of the polyurethane prepolymer used in Example 1, 62.4 p.b.w. of the mixed diazo condensate described in Example 2, 3.0 p.b.w. of 85% phosphoric acid, and 3.0 p.b.w. of Crystal Violet and ethyleneglycol monomethyl ether.
The solution is applied, as a layer weighing 1.5 g/m2, to an eloxated aluminum support (weight of the oxide layer: 2 g/m ), pre-treated with polyvinyl phosphonic acid as describecl in Example 1.
-- 2~ --Z K - 2 fi 8 7 By exposing the material for 80 seconds under a negative ori~
nal, using the metal halide lamp described in l~arnple 1 at a distance of 130 cm, and developing it for 90 seconds with the developer of Ex-ample 1, flawless copies are obtained. With an exposure time of 80 seconds, the step wedge is fully blackened up to step 5.
After development, the printing plate shows excellent contrast, so that even the finest film edges are clearly discernible.
A plate processed in this manner yields 110,000 copies on a printing machine.
Example 5 A light-sensitive copying composition is prepared from the fol-lowing components:
61.0 p.b.w. of a branched polyurethane prepolymer which contains 16 per cent of terminal free NCO groups and is obtained by reacting 4,4'-diphenylmethane-diiso-cyanate with a mixture of butane diol-(1,4), polypro-pylene glycol, and 1,1,1-trimethylol propane, 31.2 p.b.w. of the mixed diazo condensate described in Example 2, 4.0 p.b.w. of 85% phosphoric acid, 4 .0 p .b.w. of the red dyestuff used in Example 1, and 1.0 p.b.w. of Methyl Orange (C.I. 13025), dissolved in ethyleneglycol monomethyl ether.
If the layer has a thickness corresponding to a weight of 1.4 g/m and the above mentioned red dyestuff is used, an exposure time of 50 sec. (metal halide lamp) at a distance of 130 cm is required to cause step 5 of the copy of the step wedge to be fully blackened.
~fter d~velopment, the plate shows a brilliant, deeply violet contra st .
Exam~l~ 6 ~, The following components 60.0 p.b.w. of a polyurethane prepolymer with an iso-cyanate content of about 20 per cent, based on the molecular weight of ihe prepolymer, and correspond-ing to the following formula NCO
CH2-O-CO-NH- ~-CH3 / NCO
H3C-CH2-C/ CH2-O-CO-NH- ~-C~I3 NCO
\CH2-O-CO-NH- ~-CH3 30.0 p.b.w. of the mixed condensate used in Example 2, 7.5 p.b.w. of Rhodamine 6 GDN extra (C.I. 45160), and 3.3 p.b.w. of 85% phosphoric acid were applied, as a S per cent solution in ethyleneglycol monomethyl ether, onto an anodized support, so that the resulting layer weighed 1.0 ~/m2. After 30 seconds' exposure to a metal halide lamp at a dis-tance of 130 cm and development with the developer used in Example 1, a run of 70,000 copies could be printed.
The layer shows an exceptionally steep gradation corresponding to only one half tone step of the step wed~e.
Example 7 33 .0 p .b.w. of the polyurethane prepolymer described in Example 1, 25.0 p.b.w. of the alkyd resin used in Example 3, 3.4 p.b.w. of polyvinyl formal, 35.2 p.D.W. of the mixed diazo condensate described in Example 2, K- 2 1 ~ 7 3.0 p.b.w. of 85% phosphoric acid, 3.0 p.b.w. of Rhodamine 6 GDN extra (C.I, 45160), and 0.8 p.b.w. of Metanil Yellow (C.I. 13065) are dissolved in 2000.0 p.b.w. of ethyleneglycol monomethyl ether.
A layer weighing 1.0 g/m2 is applied to wet-brushed aluminum which had been treated with polyvinyl phosphonic acid as described in Example 1. After 45 seconds' exposure under a negative original to the light of a metal halide lamp at a distance of 130 cm, the layer is de-veloped for 45 seconds with the developer used in Example 1. Excel-lent copies are produced which yield 35,000 prints in a printing machine .
Even after three months' storage, the properties of the copying layer are unchanged.
Example 8 A 5% solution in ethyleneglycol monomethyl ether is prepared from the following components:
30.0 p.b.w. of the polyurethane prepolymer described in Example 1, 28.0 p.b.w. of the allcyd resin described in Example 3, 30.0 p.b.w. of the mixed diazo condensate described in Example 2, 4.0 p.b.w. of 85% phosphoric acid, 3.0 p.b.w. of a pigment dispersion composed of 10 per cent by weight of "llostaperm Blue B G" (C.I.
74160) and 10 per cent by weight of polyvinyl formal and 80 per cent by weight of cthylene glycol methyl ether acetate, and 1.0 p.b.w. of Metallil Yellow (C.I. 13065), - 27 - .
2 K - 2 ~ 3 7 and the solution is whirler-coated onto an eloxated aluminum support which had been pretreated with polyvinyl phosphonic acid as described in Example 1, to produce a layer weighing 1~2 g/m .
After 30 seconds' exposure to a metal halide lamp from a dis-tance of 130 cm, the layer may be developed within 90 seconds with the developer mentioned in Example 1.
The copies thus produced have a good contrast which does not noticeably diminish even after five times the developing time.
Printing runs of 130,000 copies were printed on a printing ma-chine. The properties of the copying layer are still good after 50 days' storage at a temperature of 42 C and a humidity of 62%.
Example 9 61.0 p.b,w. of the polyurethane prepolymer described in Example 1, 31.2 p.b.w. of the condensation product of an aromatic diazonium compound used in Example 2, 4.0 p.b.w. of ~5% phosphoric acid, 4.0 p.b.w. of Rhodamine 6 GDN extra (C.I. 45160), and 1.0 p.b.w. of MetanilYellow (C.I. 13065) are dissolved in ethyleneglycol monomethyl ether.
This solution is then coated onto a support of electrochemically roughened and anodized aluminum with an oxide layer of 3 g/m2, which had been pretreated with polyvinyl phosphonic acid as described in Example 1.
The dry weight of the layer is between 1.0 and 1.4 g/m2. For the preparation of a lithographic printing plat'e, the following procedure is employed:
The negative-wor~ing reproduction layer is exposed for ~0 sec-onds under a necJative original to the light of a metal halide lamp at a -- 2~3 --distance of 130 cm and is then treated with the developer used in Exam-ple 1.
From the resultiny printing form, a run of more than 100,000 flawless prints may be printed on a printing machine.
Example 10 A coating solution is prepared from 30. 0 p .b.w. of the polyurethane prepolymer described in Example 1, 60.0 p.b.w. of the mixed diazo condensate described in Example 2, .0 p.b.w. of 85% phosphoric acid, and 2.0 p.b.w. of the red dyestuff used in Example 1, dissolved in ethylene glycol monomethyl ether, and the resulting solution is applied to a 50~m thick, biaxially stretched polyethylene terephthalate film in such a manner that the applied layer weighs 3.5 g/m2 The coated film is exposed for 3 minutes under a negative origi-nal, using an exposure device (8 kW Xenokop apparatus of Messrs .
Klimsch ~ Co.) at a distance of 75 cm, and is then developed for 90 seconds with the developer used in Example 1. An excellent copy is produced .
If four solutions prepared from the polyurethane prepolymer men-tioned in Example 1, a mixed diazo condensate, and phosphoric acid are dyed in the four primary colors yellow, red, blue, and black, and the four solutions are then used for coating polyester films, color proofing foils are obtained which may be used for a negative-working color proofin~ system according to the overlay principle.
For this purpose, the individual color proofing films are exposed under the corresponding silver halide color separations, developed with ~ Tr~ rK
the cleveloper of Example 1, and the resulting color ima~es are careflllly dried. If the resulting four images are superimposed in register with each other, a four-colored image corresponding to the original is pro-duced .
Example 1 1 A coating solution is prepared from the following components:
28.8 p.b.w. of the polyurethane prepolymer described in Example 1, 25 . 0 p .b .w . of the alkyd resin described in Example 3, 3.0 p.b.w. of polyvinyl formal, 30.0 p.b.w. of the mixed diazo condensate described in Example 2, 4.0 p.b.w. of 85% phosphoric acid, in 92.0 p.b.w. of ethyleneglycol monomethyl ether, and 46.C p.b.w. of ethyleneglycol methyl ether acetate.
The resulting solution is applied as a layer weighing 1.4 g/m2 to a polyethylene terephthalate film which had been hydrophilized by a silica treatment according to German Au s lege schrift No . 1, 2 2 8, 414 .
For this hydrophilizing treatment, the surface of the film is treated with a mixture comprising 1) an aqueous solution of dichloro acetic acid or trichloro acetic acid or 2,2,3-trichloro propionic acid, 2) very finely divided pyrogenic silica obtained in the gaseous phase, and 3) a con-ventional wetting agent which is resistant to the action of acids and heat, and is then dried. After exposure (45 seconds at a distance of 75 cm, using a Xenokop apparatus of 8 kW) and development as in Ex-ample 1, flawlcss copies result. Treatment with an image intensifier may be combined with the application o~ a preserving sohltion.
Examplc 12 30.0 p.b.w. of the polyurcthane prepolymer described in Example 1, 60.0 p.b.w. of the mixed diazo condensate described in Example 2, 4.0 p.b.w. of 85/~, phosphoric acid, and 4.0 p.b.w. of the red dyestuff used in Example 1, are dissolved in 900 p.b.w. of ethyleneglycol monomethyl ether and applied, as a layer weighing 3 g/m, to a zinc plate cleaned by means of a 0.3 per cent nitric acid solution. The plate is then exposed for 3 minutes, at a distance of 75 cm, to an 8 kW xenon lamp under a nega-tive original, developed with the developer used in Example 1, and finally etched with 7.5% nitric acid. The hardened image areas form an excellent etch resist.
Example 13 34.5 p.b.w. of the polyurethane prepolymer described in Example 1, 11.5 p.b.w. of a mixed diazo condensate prepared from a solution of 32.3 g of 3-methoxy-diphenyl-amine-4-diazonium sulfate in 100 ml of 86% phosphoric acid to which 25 . 8 g of 4 ,4'-bis-methoxymethyl-diphenyl ether are dropwise added. After 17 hours' condensation at ~0C, the methane sulfonate was separated, purified and dried. This method of preparation is described in Example 4 of German Offenlegungsschrift No . 2, 041, 395;
2.4 p.b.w. of 85% phosphoric acid, 1.6 p.b.w. of Crystal Violet tc~I~ 42555), in 900.0 p.b.w. of ethyleneglycol monomethyl ether.
The solution is applied, as a layerweighing 1.0 g/m, to an anodi7ed aluminum support corresponding to the one used in Example 1.
Z
The copying layer is exposed for 25 seconds under 2 negative original to the metal halide lamp described in Example 1 (clistance: 130 cm) ancl then developed with the cleveloper used in Example 1.
The plate thus obtained shows good contrast and is ready for printing .
It will be obvious to those skilled in the art that many modifica-tions may be made within the scope of the present invention without departing from the spirit thereof, and the invention includes all such modifications .
Claims (12)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A light-sensitive copying composition comprising a diazonium salt condensation product, an acid stabilizer, and a branched polyurethane prepolymer with free terminal isocyanate groups.
2. A copying composition according to claim 1 in which the proportion of free terminal isocyanate groups in the polyurethane is between 1 and 30 per cent by weight.
3. A copying composition according to claim 1 in which the stabilizer in an acid.
4. A copying composition according to claim 1 in which the acid is selected from the group consisting of phosphoric acid, sulfuric acid, perchloric acid, boric acid, and p-toluene sulfonie acid.
5. A copying composition according to claim 1 in which the diazonium salt condensation product is a reaction product of a diarylamine-4-diazonium salt and formaldehyde.
6. A copying composition according to claim 1 in which the diazonium salt condensation product is a mixed condensate which contains at least one unit each of the general types A(-D)n and B
which are linked by a bivalent intermediate member derived from a carbonyl compound capable of condensation, and wherein A is the radical of a compound containing at least two carbocyclic and/or heterocyclic aromatic rings and being capable of condensation in at least one position of its molecule with an active carbonyl compound in an acid medium, D is a diazonium salt group linked to an aromatic carbon atom of A, n is an integer from 1 to 10, and B is a radical of a compound free of diazonium groups and being capable of condensation in at least one position of its molecule with an active carbonyl compound in an acid medium.
which are linked by a bivalent intermediate member derived from a carbonyl compound capable of condensation, and wherein A is the radical of a compound containing at least two carbocyclic and/or heterocyclic aromatic rings and being capable of condensation in at least one position of its molecule with an active carbonyl compound in an acid medium, D is a diazonium salt group linked to an aromatic carbon atom of A, n is an integer from 1 to 10, and B is a radical of a compound free of diazonium groups and being capable of condensation in at least one position of its molecule with an active carbonyl compound in an acid medium.
7. A copying composition according to claim 6 in which the anion of the diazonium salt condensation product is the anion of an aliphatic monosulfonic acid with 1 to 6 carbon atoms.
8. A copying composition according to claim 1 which additionally contains a non-drying alkyd resin.
9. A copying composition according to claim 1 in which the poly-urethane is present in the copying composition in a quantity between 30 and 80 per cent by weight.
10. A copying composition according to claim 1 in which the diazo compound is present in the copying composition in a quantity between 20 and 70 per cent by weight.
11. A copying composition according to claim 1 in the form of a light-sensitive layer on a support.
12. A copying composition according to claim 11 in which the support is aluminum.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU75.749 | 1976-09-08 | ||
| LU75749A LU75749A1 (en) | 1976-09-08 | 1976-09-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1112092A true CA1112092A (en) | 1981-11-10 |
Family
ID=19728347
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA286,118A Expired CA1112092A (en) | 1976-09-08 | 1977-09-06 | Light-sensitive copying composition including a branched polyurethane prepolymer with free terminal isocyanate groups |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US4186017A (en) |
| JP (1) | JPS5333116A (en) |
| AT (1) | AT354843B (en) |
| AU (1) | AU520188B2 (en) |
| BE (1) | BE858410A (en) |
| BR (1) | BR7705952A (en) |
| CA (1) | CA1112092A (en) |
| DE (1) | DE2739774A1 (en) |
| DK (1) | DK398377A (en) |
| ES (1) | ES462165A1 (en) |
| FR (1) | FR2364488A1 (en) |
| GB (1) | GB1589225A (en) |
| LU (1) | LU75749A1 (en) |
| NL (1) | NL7709745A (en) |
| PT (1) | PT67011B (en) |
| SE (1) | SE7709953L (en) |
| ZA (1) | ZA775351B (en) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2809774A1 (en) * | 1978-03-07 | 1979-09-13 | Hoechst Ag | METHOD AND DEVELOPER SOLUTION FOR DEVELOPING EXPOSED LIGHT-SENSITIVE COPY LAYERS |
| DE2948554A1 (en) * | 1979-12-03 | 1981-06-04 | Hoechst Ag, 6000 Frankfurt | LIGHT SENSITIVE MIXTURE |
| DE3036077A1 (en) * | 1980-09-25 | 1982-05-06 | Hoechst Ag, 6000 Frankfurt | LIGHT-CURABLE MIXTURE AND LIGHT-SENSITIVE COPY MATERIAL MADE THEREOF |
| US4729935A (en) * | 1982-03-18 | 1988-03-08 | Hoechst Celanese Corporation | Process for the production of photographic images utilizing a negative working diazo contact film |
| US4448873A (en) * | 1982-03-18 | 1984-05-15 | American Hoechst Corporation | Negative working diazo contact film |
| DE3364925D1 (en) * | 1982-06-03 | 1986-09-04 | Hoechst Co American | Photosensitive composition developable with water, and photosensitive copying material produced therefrom |
| JPS59222842A (en) * | 1983-06-01 | 1984-12-14 | Fuji Photo Film Co Ltd | Photosensitive composition for lithographic plate |
| US4544466A (en) * | 1983-12-06 | 1985-10-01 | Phillips Petroleum Company | Process of making U.V. cured polyurethanes using diazonium salt promoters |
| US4549945A (en) * | 1984-01-11 | 1985-10-29 | Phillips Petroleum Company | UV Cured polyurethanes using organotin promoters |
| DE3409888A1 (en) * | 1984-03-17 | 1985-09-19 | Hoechst Ag, 6230 Frankfurt | LIGHT-SENSITIVE RECORDING MATERIAL AND USE THEREOF IN A METHOD FOR PRODUCING A PRINTING FORM OR PRINTED CIRCUIT |
| GB8414867D0 (en) * | 1984-06-11 | 1984-07-18 | Minnesota Mining & Mfg | Pre-press proofing system |
| JPH0782236B2 (en) * | 1984-10-12 | 1995-09-06 | 三菱化学株式会社 | Photosensitive composition |
| CA1308595C (en) * | 1985-11-22 | 1992-10-13 | Toshiaki Aoai | Photosensitive composition |
| US4877711A (en) * | 1986-05-19 | 1989-10-31 | Fuji Photo Film Co., Ltd. | Light-sensitive diazo photopolymerizable composition with polyurethane having carbon-carbon unsaturated and a carboxyl group |
| DE3644163A1 (en) * | 1986-12-23 | 1988-07-07 | Hoechst Ag | LIGHT SENSITIVE MIXTURE BASED ON A DIAZONIUM SALT POLYCONDENSATION PRODUCT AND LIGHT SENSITIVE RECORDING MATERIAL MADE THEREOF |
| JP2810998B2 (en) * | 1987-10-15 | 1998-10-15 | コニカ 株式会社 | Photosensitive composition |
| JPH01102456A (en) * | 1987-10-15 | 1989-04-20 | Konica Corp | Photosensitive composition |
| JPH01102457A (en) * | 1987-10-15 | 1989-04-20 | Konica Corp | Photosensitive composition |
| JP2622711B2 (en) * | 1988-03-28 | 1997-06-18 | 三菱化学株式会社 | Photosensitive composition |
| JP2657516B2 (en) * | 1988-04-05 | 1997-09-24 | コニカ株式会社 | Photosensitive composition |
| JP2671406B2 (en) * | 1988-07-19 | 1997-10-29 | 三菱化学株式会社 | Photosensitive composition |
| JP2768692B2 (en) * | 1988-08-01 | 1998-06-25 | 株式会社日立製作所 | Radiation-sensitive composition and pattern forming method |
| DE3841025A1 (en) * | 1988-12-06 | 1990-06-07 | Hoechst Ag | POLYMERIZABLE MIXTURE BY RADIATION AND RECORDING MATERIAL MADE THEREOF |
| US5242779A (en) * | 1989-06-21 | 1993-09-07 | Hoechst Aktiengesellschaft | Photosensitive mixture containing photocurable compound and polyurethane binder with grafted vinyl alcohol units, carboxylic acid vinyl ester units and vinyl acetal units |
| DE3920230A1 (en) * | 1989-06-21 | 1991-01-24 | Hoechst Ag | LIGHT-SENSITIVE MIXTURE AND LIGHT-SENSITIVE RECORDING MATERIAL MANUFACTURED THEREFROM |
| DE3920229A1 (en) * | 1989-06-21 | 1991-01-03 | Hoechst Ag | PHOTOPOLYMERIZABLE MIXTURE AND RECORDING MATERIAL MADE THEREOF |
| US5238772A (en) * | 1989-06-21 | 1993-08-24 | Hoechst Aktiengesellschaft | Photopolymerizable mixture and recording material containing free-radically polymerizable compound, photosensitive polymerization initiator and polyurethane binder grafted with vinyl alcohol and vinyl acetal units |
| JP2687018B2 (en) * | 1989-08-31 | 1997-12-08 | 富士写真フイルム株式会社 | Photosensitive composition |
| US5232813A (en) * | 1990-01-31 | 1993-08-03 | Fuji Photo Film Co., Ltd. | Ps plate for use in making lithographic printing plate requiring no dampening water utilizing irradiation cured primer layer containing polyurethane resin and diazonium salt polycondensate photopolymerizable light-sensitive layer and silicone rubber layer |
| JP2627565B2 (en) * | 1990-02-19 | 1997-07-09 | 富士写真フイルム株式会社 | Photosensitive lithographic printing plate |
| JPH03240060A (en) * | 1990-02-19 | 1991-10-25 | Fuji Photo Film Co Ltd | Photosensitive planographic printing plate |
| JP2681418B2 (en) * | 1990-02-21 | 1997-11-26 | 富士写真フイルム株式会社 | Lithographic printing plate manufacturing method |
| JPH03290663A (en) * | 1990-04-09 | 1991-12-20 | Fuji Photo Film Co Ltd | Photosensitive composition |
| JPH03296756A (en) * | 1990-04-16 | 1991-12-27 | Fuji Photo Film Co Ltd | Image forming method |
| JP2709532B2 (en) * | 1991-03-01 | 1998-02-04 | 富士写真フイルム株式会社 | Photosensitive lithographic printing plate |
| DE4439184A1 (en) | 1994-11-03 | 1996-05-09 | Hoechst Ag | Photosensitive recording material |
| US6638679B2 (en) * | 2001-07-12 | 2003-10-28 | Kodak Polychrome Graphics, Llc | Photosensitive compositions having mixtures of alkoxy and non-alkoxy diazonium salt containing compounds |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2770612A (en) * | 1952-01-23 | 1956-11-13 | Goodrich Co B F | Elastomeric dhsocyanate-modified polyesters |
| US3208850A (en) * | 1962-04-11 | 1965-09-28 | Kalvar Corp | Vesicular type photographic materials comprising a polyurethane resin containing light decomposable compounds |
| US3867147A (en) * | 1969-05-20 | 1975-02-18 | Hoechst Co American | Light-sensitive diazo compounds and reproduction material employing the same |
| US3644289A (en) * | 1969-05-29 | 1972-02-22 | Upjohn Co | Light sensitive polyurethanes prepared from hydroxyl containing polymer and an isocyanato-stilbene compound |
| US3655625A (en) * | 1969-07-28 | 1972-04-11 | Lithoplate Inc | Polyurethane-cinnamate photopolymer |
| US3660097A (en) * | 1969-11-28 | 1972-05-02 | Polychrome Corp | Diazo-polyurethane light-sensitive compositions |
| JPS5034964B1 (en) * | 1970-03-30 | 1975-11-12 | ||
| DE2053363C3 (en) * | 1970-10-30 | 1980-09-18 | Hoechst Ag, 6000 Frankfurt | Photosensitive mixture |
| IT1000315B (en) * | 1972-12-14 | 1976-03-30 | Polychrome Corp | IMPROVEMENT IN POTOSENSITIVE UNSATURATED DIAZOIC MONOMERE COMPOSITIONS |
| NL177718C (en) * | 1973-02-22 | 1985-11-01 | Siemens Ag | METHOD FOR MANUFACTURING RELIEF STRUCTURES FROM HEAT-RESISTANT POLYMERS |
-
1976
- 1976-09-08 LU LU75749A patent/LU75749A1/xx unknown
-
1977
- 1977-08-31 AU AU28408/77A patent/AU520188B2/en not_active Expired
- 1977-09-03 DE DE19772739774 patent/DE2739774A1/en active Granted
- 1977-09-05 BE BE180680A patent/BE858410A/en not_active IP Right Cessation
- 1977-09-05 SE SE7709953A patent/SE7709953L/en unknown
- 1977-09-05 FR FR7726804A patent/FR2364488A1/en active Granted
- 1977-09-05 NL NL7709745A patent/NL7709745A/en not_active Application Discontinuation
- 1977-09-06 GB GB37161/77A patent/GB1589225A/en not_active Expired
- 1977-09-06 ES ES462165A patent/ES462165A1/en not_active Expired
- 1977-09-06 ZA ZA00775351A patent/ZA775351B/en unknown
- 1977-09-06 AT AT639877A patent/AT354843B/en not_active IP Right Cessation
- 1977-09-06 CA CA286,118A patent/CA1112092A/en not_active Expired
- 1977-09-06 US US05/830,771 patent/US4186017A/en not_active Expired - Lifetime
- 1977-09-06 BR BR7705952A patent/BR7705952A/en unknown
- 1977-09-07 PT PT67011A patent/PT67011B/en unknown
- 1977-09-07 DK DK398377A patent/DK398377A/en not_active Application Discontinuation
- 1977-09-08 JP JP10833677A patent/JPS5333116A/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| NL7709745A (en) | 1978-03-10 |
| ZA775351B (en) | 1978-07-26 |
| PT67011B (en) | 1979-02-13 |
| AT354843B (en) | 1979-01-25 |
| ATA639877A (en) | 1979-06-15 |
| BE858410A (en) | 1978-03-06 |
| BR7705952A (en) | 1978-06-27 |
| US4186017A (en) | 1980-01-29 |
| FR2364488B1 (en) | 1980-01-18 |
| DE2739774C2 (en) | 1989-11-30 |
| GB1589225A (en) | 1981-05-07 |
| AU2840877A (en) | 1979-03-08 |
| ES462165A1 (en) | 1978-11-01 |
| FR2364488A1 (en) | 1978-04-07 |
| LU75749A1 (en) | 1978-04-27 |
| PT67011A (en) | 1977-10-01 |
| DK398377A (en) | 1978-03-09 |
| AU520188B2 (en) | 1982-01-21 |
| JPS5333116A (en) | 1978-03-28 |
| DE2739774A1 (en) | 1978-03-09 |
| SE7709953L (en) | 1978-03-09 |
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| MKEX | Expiry |