CA1300294C - Radiation-polymerizable composition - Google Patents
Radiation-polymerizable compositionInfo
- Publication number
- CA1300294C CA1300294C CA000502905A CA502905A CA1300294C CA 1300294 C CA1300294 C CA 1300294C CA 000502905 A CA000502905 A CA 000502905A CA 502905 A CA502905 A CA 502905A CA 1300294 C CA1300294 C CA 1300294C
- Authority
- CA
- Canada
- Prior art keywords
- composition
- monomer
- polyvinyl
- polymerizable mixture
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- 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
- G03F7/09—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers
- G03F7/095—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers having more than one photosensitive layer
- G03F7/0955—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers having more than one photosensitive layer one of the photosensitive systems comprising a non-macromolecular photopolymerisable compound having carbon-to-carbon double bonds, e.g. ethylenic compounds
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Engineering & Computer Science (AREA)
- Architecture (AREA)
- Structural Engineering (AREA)
- General Physics & Mathematics (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
- Polymerisation Methods In General (AREA)
Abstract
Abstract of the Disclosure This invention relates to a radiation polymerizable composition for use in a photographic element such as a lithographic printing plate comprising in admixture a) a polymeric binder;
b) a photoinitiator;
c) a diazonium salt; and d) a photopolymerizable mixture of i) a polyfunctional acrylic monomer having from 3 to 6 unsaturated groups; and ii) a monofunctional acrylic monomer having 1 unsaturated group.
b) a photoinitiator;
c) a diazonium salt; and d) a photopolymerizable mixture of i) a polyfunctional acrylic monomer having from 3 to 6 unsaturated groups; and ii) a monofunctional acrylic monomer having 1 unsaturated group.
Description
29~
Bac~ground of the Invention The present invention relates to a radiation-polymer-izable composi-tion. More particularly, this invention relates to a radiation-polymerizable composition which may be empolyed to produce an improved photographic element such as a lithographic printing plate. Such plates show an increase of stability and ; press run life.
The basic difference in the various approaches in the formulation of lithographic printing plates from radiation poly-merizable compositions has been in the search for a system whichis prepared from relatively inexpensive ingredients, does not require prolonged imaging cycles (has a high quantum efficiency), is able to undergo an increased number of press runs and results in the creation of high resolution images within the composition which can be manifested without prolonged and elaborate development.
Most such lithographic printing plates comprise a metal substrate which is coated with a light sensitive diazonium compound in admixture with suitable binding resins, photoinitia-tors, photopolymerizable compositions, colorants, stabilizers,exposure indicators, surfactants and the like.
Although the art is replete with photosensitive compo-sitions which may be used for lithographic printing plates, the prior art composition's serviceability is restricted by their limited stability and number of press runs.
13~294 Summary of the Invention This invention relates to a radiation polymerizable composition for use in forming photographic elements such as lithographic printing plates, comprising in admixture a) a polymeric binder;
b) a photoinitiator;
c) a diazonium salt; and d) a polymerizable mixture of i) a polyfunctional acrylic monomer having from 3 to 6 unsaturated groups; and ii) a monofunctional acrylic monomer having 1 unsaturated group.
Detailed Description of the Invention `~ The polymeric binder useful in the practice of this invention is preferably characterized as being a polymer which does not react with itself or other compounds when exposed to actinic radiation. The preferred binder resin should be sub-stantially organic solvent soluble and is preferably one which is not substantially alkali, acid or water soluble. The binder must have a molecular weight sufficient to provide a tack-free surface when in admixture with the photopolymerizable mixture and to pro-vide a tough cohesive matrix which when used to produce a lithographic printing plate is capable of providing numerous quality impressions. The molecular weight must be low enough, though, to permit solubility in formulation as well as during development. The molecular weight of the binder should be ~3~ 294 greater than about 20,000, preferably greater than about 30,000 and, most preferably, greater than about 40,000.
Examples of binders suitable for this invention include epoxy resins, polyvinyl acetate, polyvinyl acetals (e.g. polyvinyl butyral), polyesters, polyamides, polyethers, polyurethanes and polyacrylic resins which are either homo- or copolymers of acryl-ates (or methacrylates) and/or acrylic acid (or methacrylic acid).
In the preferred embodiment, the polymeric binder is a terpolymer of polyvinyl acetate, polyvinyl alcohol and polyvinyl formal available as Formvar* 12/85 from Monsanto of St. Louis, Missouri.
Preferably, the polymeric binder is present in the composition at a percent solids level of from about 20% to about 75% by weight. A more preferred range is from about 30% to about 65~ by weight and, most preferably, the polymeric binder is present at a percent solids level of from about 35% to about 50%
by weight.
Suitable photoinitiators which may be used in this invention are preferably those free-radical photoinitiators having an absorption maximum in the range of from about 320 to about 400nm. Examples include the acetophenones, benzophenones, tria-zines, benzoins, benzoin ethers, xanthones, -thioxanthones, acridines and benzoquinones. More preferred of these are the triazines having the formula CCl3 N- C
Ar - CH = CH - ~ C
CCl3 *Trade-Marks - 3 -C
~10029~
wherein Ar is and Rl, R2, R3 and R4 arer independently, hydrogen, chlorine, bromine, alkoxy, or alkyl. The most preferred photoinitiator is
Bac~ground of the Invention The present invention relates to a radiation-polymer-izable composi-tion. More particularly, this invention relates to a radiation-polymerizable composition which may be empolyed to produce an improved photographic element such as a lithographic printing plate. Such plates show an increase of stability and ; press run life.
The basic difference in the various approaches in the formulation of lithographic printing plates from radiation poly-merizable compositions has been in the search for a system whichis prepared from relatively inexpensive ingredients, does not require prolonged imaging cycles (has a high quantum efficiency), is able to undergo an increased number of press runs and results in the creation of high resolution images within the composition which can be manifested without prolonged and elaborate development.
Most such lithographic printing plates comprise a metal substrate which is coated with a light sensitive diazonium compound in admixture with suitable binding resins, photoinitia-tors, photopolymerizable compositions, colorants, stabilizers,exposure indicators, surfactants and the like.
Although the art is replete with photosensitive compo-sitions which may be used for lithographic printing plates, the prior art composition's serviceability is restricted by their limited stability and number of press runs.
13~294 Summary of the Invention This invention relates to a radiation polymerizable composition for use in forming photographic elements such as lithographic printing plates, comprising in admixture a) a polymeric binder;
b) a photoinitiator;
c) a diazonium salt; and d) a polymerizable mixture of i) a polyfunctional acrylic monomer having from 3 to 6 unsaturated groups; and ii) a monofunctional acrylic monomer having 1 unsaturated group.
Detailed Description of the Invention `~ The polymeric binder useful in the practice of this invention is preferably characterized as being a polymer which does not react with itself or other compounds when exposed to actinic radiation. The preferred binder resin should be sub-stantially organic solvent soluble and is preferably one which is not substantially alkali, acid or water soluble. The binder must have a molecular weight sufficient to provide a tack-free surface when in admixture with the photopolymerizable mixture and to pro-vide a tough cohesive matrix which when used to produce a lithographic printing plate is capable of providing numerous quality impressions. The molecular weight must be low enough, though, to permit solubility in formulation as well as during development. The molecular weight of the binder should be ~3~ 294 greater than about 20,000, preferably greater than about 30,000 and, most preferably, greater than about 40,000.
Examples of binders suitable for this invention include epoxy resins, polyvinyl acetate, polyvinyl acetals (e.g. polyvinyl butyral), polyesters, polyamides, polyethers, polyurethanes and polyacrylic resins which are either homo- or copolymers of acryl-ates (or methacrylates) and/or acrylic acid (or methacrylic acid).
In the preferred embodiment, the polymeric binder is a terpolymer of polyvinyl acetate, polyvinyl alcohol and polyvinyl formal available as Formvar* 12/85 from Monsanto of St. Louis, Missouri.
Preferably, the polymeric binder is present in the composition at a percent solids level of from about 20% to about 75% by weight. A more preferred range is from about 30% to about 65~ by weight and, most preferably, the polymeric binder is present at a percent solids level of from about 35% to about 50%
by weight.
Suitable photoinitiators which may be used in this invention are preferably those free-radical photoinitiators having an absorption maximum in the range of from about 320 to about 400nm. Examples include the acetophenones, benzophenones, tria-zines, benzoins, benzoin ethers, xanthones, -thioxanthones, acridines and benzoquinones. More preferred of these are the triazines having the formula CCl3 N- C
Ar - CH = CH - ~ C
CCl3 *Trade-Marks - 3 -C
~10029~
wherein Ar is and Rl, R2, R3 and R4 arer independently, hydrogen, chlorine, bromine, alkoxy, or alkyl. The most preferred photoinitiator is
2-stilbenyl-4,6-di(trichloromethyl) triazine.
The photoinitiator is preferably present ln the composition at a percent solids level of about 1.5% to about 8.0%
by weight, more preferably about 2.0% to about 6.0% by weight and is most preferably present at a percent solids level of from about
The photoinitiator is preferably present ln the composition at a percent solids level of about 1.5% to about 8.0%
by weight, more preferably about 2.0% to about 6.0% by weight and is most preferably present at a percent solids level of from about
3.0% to about 4.0% by weight.
The diazonium salt which is useful in the practice of this invention may be any suitable light-sensitive diazonium poly-meric or monomeric compound which are well known to the s~illed artisan although the polymeric diazonium compounds are preferred.
Suitable diazonium compounds include those condensed with formal-dehyde such as disclosed in United States 2,063,631 and 2,667,415, the polycond~nsation products such as disclosed in United States 3,849,392 and 3,867,147, and the high speed diazos such as dis-closed in United States 4,436,804.
U.S. Patent 4,436,804 describes a diazoniu~ salt which is the condensation product oi 4,4'-bis-methoxymethyl diphenyl ether, which is first precondensed with itself to form an oligomer having from 2 to 10 repeatin~ units, and 3-methoxy-diphenylamine-
The diazonium salt which is useful in the practice of this invention may be any suitable light-sensitive diazonium poly-meric or monomeric compound which are well known to the s~illed artisan although the polymeric diazonium compounds are preferred.
Suitable diazonium compounds include those condensed with formal-dehyde such as disclosed in United States 2,063,631 and 2,667,415, the polycond~nsation products such as disclosed in United States 3,849,392 and 3,867,147, and the high speed diazos such as dis-closed in United States 4,436,804.
U.S. Patent 4,436,804 describes a diazoniu~ salt which is the condensation product oi 4,4'-bis-methoxymethyl diphenyl ether, which is first precondensed with itself to form an oligomer having from 2 to 10 repeatin~ units, and 3-methoxy-diphenylamine-
4-diazonium sulfate. In a preferred embodiment in the prac~ice of this invention the diazonium salt is the condensation product of ~ ` _ ~ _ ~ V
`` ~l3~294 4,4'-bis-methoxymethyl diphenyl ether, which is first precondensed with itself to form an oligomer having from 2 to 7 repeating units, and 3-methoxy-diphenylamine-4-diazonium sulphate.
Preferably, the diazonium salt comprises the 1:1 poly-condensation product of 3-methoxy-diphenylamine-4-diazonium - 4a -~3~9~
sulphate and 4,4'-bis-methoxymethyl, diphenyl ether, precipitated as the mesitylene sulfonate, such as is taught in United States 3,849,392.
The diazonium salt is preferably present in the composi-tion of the subject invention at a percent solids level of from about 3% to about 20% by weight. More preferably it is present at about 5% to about 18% by weight and most preferably the diazonium salt is present at a percent solids level of from about 10% to about 15% by weight.
The polymerizable mixture of the subject invention is comprised of , in admixture, a polyfunctional acrylic monomer which has from 3 to 6 unsaturated groups and a monofunctional acrylic monomer which has 1 unsaturated group.
The polyfunctional acrylic monomer is an ethylenically unsaturated compound having from three to six unsaturated groups and being capable of reacting with the monofunctional acrylic monomer upon exposure to imaging radiation. The polyfunctional monomer is characterized as having the unsaturated groups being acrylate or methacrylate esters. The preferred monomer is either a solid or liquid having a viscosity of greater than about 700mPa.S at 25C, preferably greater than about 2000mPa.s at 25C.
Most preferably, the monomer has a viscosity of greater than about 4000mPa.S at 25C.
Examples of compounds which are suitable for use as the polyfunctional acrylic monomer of this invention include trimethyl propane triacrylate and the ethoxylated or propoxylated homologs thereof, trimethylol propane tri-methacrylate and the ethoxylated ~3~Z~
or propoxylated analogs thereof, pentaerythritol triacrylate, pentaerythritol trimethacrylate, dipentaerythritol monohydroxy pentaacrylate, dipentaerythritol monohydroxy pentamethacrylate, dipentaerythritol hexaacrylate, dipentaerythritol hexamethacrylate, pentaerythritol tetraacrylate and pentaerythritol tetramethacry-late. Preferably, the monomer is pentaerythritol tetraacrylate, although a combination of suitable monomers is also advantageous.
The monofunctional monomer is an ethylenically unsaturated compound having one unsaturated group and is capable of reacting with the polyfunctional monomer upon exposure to imaging radiation. The monofunctional monomer is characterized as having the unsaturated group being an acrylate or methacrylate ester. Preferably, the monofunctional monomer is a liquid having a viscosity in the range of from about 1 to about 25 mPa.s at 25C.
Examples of compounds which are suitable for use as the monofunctional monomer of this invention include trimethylol : propane monoacrylate and the ethoxylated or propoxylated homologs thereof, trimethylol propane monomethacrylate and the ethoxylated or propoxylated homologs thereof, pentaerythritol acrylate, pentaerythritol methacrylate, tetrahydro furfuryl acrylate, tetrahydro furfuryl methacrylate, cyclohexyl acrylate, cyclohexyl methacrylate, n-hexyl acrylate, n-hexyl methacrylate, glycidyl acrylate and glycidyl methacrylate. Preferably, the monomer is : pentaerythritol monoacrylate, although a combination of suitable ~ monomers is also advantageous.
~3~D29~
In the polymerizable mixture of this invention the polyfunctional monomer should be present in an amount of more than at least about 50% and, more preferably, should be present in an amount of from about 65% to about 80%,based on the total weight of the monofunctional and polyfunctional monomers. The monofunctional monomer should comprise the balance of the poly-merizable mixture.
The polymerizable mixture is present at a percent solids level which is preferably in the range of from about 20% to about 70~ by weight. More preferably, the polymerizable mixture is present at a percent solids level of from about 30% to about 60%
by weight and most preferably from about 30% to about 50% by weight.
One of the advantages in having a polyfunctional monomer in the polymerizable mixture in combination with a monofunctional monomer is that the 3-dimensional structure provided by the polyfunctional monomer provides good matrix integrity allowing for a tough image and the linear propagation provided by the monofunctional monomer provides good photospeed. If the polymerizable mixture was comprised of two polyfunctional acrylic monomers, the resulting image would have good toughness but poor photospeed. If the mixture was comprised of two monofunctional acrylic monomers, there would be good photospeed but poor image toughness.
One of the significant aspects of this invention is that the unique combination of photoinitiator, diazonium salt and polymerizable mixture reduces the need for use of an oxygen 2~91 barrier layer or the necessity for processing in a nitroyen environment, although the exact mechanism for this is unclear.
Among the possible advantages derived thereby is elimination of 1) the inconvenience of applying a second coating, 2) the concern over the refractive index and solubility of the oxygen barrier layer, 3) the concern over blinding on a printing press due to residue from the oxygen barrier layer, and 4) the concern over potential image gain due to the oxygen barrier layer~
Other components which may be included in the radiation-polymerizable composition of this invention include acid stabilizers, exposure indicators, plasticizers, photoactivators and colorants.
Suitable acid stabilizers useful within the context ofthis invention include phosphoric, citric, benzoic, m-nitro benzoic, p(p-anilino phenylazo) benzene sulfonic acid, 4,4'-dini-tro-2,2'-stilbene disulfonic, itaconic, tartaric and p-toluene sulfonic acid, and mixtures thereof. Preferably, the acid stabilizer is phosphoric acid. When used, the acid stabilizer is preferably present in the radiation-polymerizable composition in the amount of from about 0.3% to about 2.0%, and most preferably from about 0.75% to about 1.5%, although the skilled artisan may use more or less as desired.
Exposure indicators (or photoimagers) which may be useful in conjunction with the present invention include 4-phenylazodiphenylamine, eosin, azobenzene, Calcozine Fuchsine~
dyes and Crystal Violet and Methylene Blue dyes. Preferably, the ~ r~
- ~3~029~
exposure indicator is 4-phenylazodiphenylamine. The exposure indicator, when one is used, is preferably present in the composition in an amount of from about 0.001% to about 0.035% by weight. A more preferred range is from about 0.002% to about 0.030% and, most preferably, the exposure indicator is present in an amount of from about 0.005% to about 0.20%, although the skilled artisan may use more or less as desired.
The photoactivator which may be included in the composition of this invention should be an amine-containing photoactivator which combines synergistically with the free-radical photoinitiator in order to extend the effective half-life of the photoinitiator, which is normally in the approximate range of about 10 9 to 10 15 seconds. Suitable photoactivators include 2-(n-butoxy) ethyl-4-dimethylamino benzoate, 2-(dimethylamino) amino benzoate and acrylated amines. Preferably the photoactivator is ethyl-4-dimethylamino benzoate. The photoactivator is preferably present in the composition of this invention in an amount of from about 1.0% to about 4.0% by weight, although the skilled artisan may use more or less as desired.
A plasticizer may also be included in the composition of this invention to prevent coating brittleness and to keep the composition pliable if desired. Suitable plasticizers include dibutylphthalate, triarylphosphate and, preferably, dioctylphathalate. The plasticizer is preferably present in the composition of this invention in an amount of from about 0.5% to about 1.25% by weight, although the skilled artisan may use more or less as desired.
Colorants useful herein include dyes such as Rhodamine, Calcozine, Victoria Blue and methyl violet, and such pigments as the anthraquinone and phthalocyanine types. Generally, the colorant is present in the form of a pigment dispersion which may comprise a mixture of one or more pigments and/or one or more dyes dispersed in a suitable solvent or mixture of solvents.
When a colorant is used, it is preferably present in the composition of this invention in an amount of from about 1.5% to about 4.0% by weight, more preferably from about 1.75% to about 3.0% and most preferably from about 2.0% to about 2.75%, although the skilled artisan may use more or less as desired.
In order to form a coating composition for the production of lithographic printing plates, the composition of this invention may be dispersed in admixture in a solvent or mixtureof solvents ; to facilitate application of the composition to the substrate.
Suitable solvents for this purpose include tetrahydrofuran, propylene glycol monomethyl ether, butyrolactone, methyl cellosolve, ethylene glycol ethers, alcohols such as ethyl 20 alcohol and n-propanol, and ketones such as methyl ethyl ketone, or mixtures thereof. Preferably, the solvent comprises a mixture of tetrahydrofuran, propylene glycol monomethyl ether and butyrolactone. In general, the solvent system is evaporated from the coating composition once it is applied to an appropriate substrate, however, some insignificant amount of solvent may remain as residue.
. .
. .
L3~29~L
~ ubstrates useful for coating with the composition of this invention to form a lighographic printing plate include sheets of transparent films such as polyester, aluminum and its alloys and other metals, silicon and similar materials which are well known in the art. Preferably, the substrate comprises aluminum. The substrate may first be pretreated by standard graining and/or etching and/or anodizing techniques as are well known in the art, and also may or may not have been treated with a composition such as polyvinyl phosphonic acid, sodium silicate or the like suitable for use as a hydrophilizing agent.
In the production of photographic elements such as lithographic printing plates, an aluminum substrate is first preferably grained by art recognized methods such as by means of a wire brush, a slurry of particulates or by chemical- or electrochemical means, for example in an electrolyte solution comprising hydrochloric acid. The grained plate is preferably then anodized for example in sulfuric or phosphoric acid in a manner well known in the art. The grained and anodized surface is preferably then rendered hydrophilic by treatment with poly-vinyl phosphonic acid by means which are also known to the skilledartisan. The thusly prepared plate is then coated with the composition of the present invention, preferably at a coating weight of from about 0.6g/m to about 2.5g/m , more preferably from about 0.8g/m to about 2.Og/m and most preferably from about 1.2g/m to about 1.5g/m , although these coa-ting weights are not critical to the practice of this invention, and dried.
~L3~)0~4 Preferably the thusly prepared lighographic printing plate is exposed to actinic radiation through a negative test flat so as to yield 6 solid steps on a 21 step Stouffer exposure wedge after development. The exposed plate is then developed with a suitable developer composition, preferably an organic solvent based developer, such as one compri.sing 2-propoxyethanol, a nonionic surfactant and an inorganic salt such as is disclosed in United States 4,308,340 and 4,381,340. In conventional use, the developed plate is finished with a subtractive finisher such as a hydrophllic polymer. Examples include cold water-soluble dextrin and/or polyvinyl pyrrolidone, a nonionic surfactant, a humectant, an inorganic salt and water, as taught by IJnited States 4,213,887.
For the purpose of improving the press performance of a plate prepared as described above, it is known that baking of the exposed and developed plate can result in an increase in the number of quality impressions over that otherwise obtainable. To properly bake the plate, it is first treated with a solution designed to prevent loss of hydrophilicity of the background during baking. An example of an effective solution is disclosed in United States 4,355,096. The thusly prepared plate is then heat treated by baXing at a temperature of from about 1~0C up to the annealing t-mperature of the substrate, most preferably about 240C. The effective baking time is inversely proportional to the temperature and averages in the range of from about 2 to ~.3~)0294 about 15 minutes. At 240C the time is about 7 minutes.
The following examples are illustrative of the invention but it is understood that the invention is not limited thereto.
None of the plates prepared in Examples 1-5 have an oxygen barrier layer thereon nor were they processed in a nitrogen environment.
Example 1 An 8" x 25" section of lithographic grade 1100 aluminum alloy is degreased with an aqueous alkaline degreasing solution and electrochemically grained using 900 coulombs of alternating current in an aqueous solution of nitric acid and aluminum nitrate.
The grained plate is well rinsed and anodized in a sulfuric acid bath wherein the aluminum is made anodic. Sufficient current and voltage is used to produce an oxide layer of 2.8g/m2. The anodized plate is well rinsed and hydrophilized by immersing the plate into a solution of polyvinyl phosphonic acid. The plate is well rinsed and dried. The thusly prepared plate is whirler coated with a solution having the following composition:
% w/w A terpolymer of polyvinyl acetate, polyvinyl alcohol and polyvinyl ~ormal commercially available as Formvar 12/85 4-54 Pentaerythritol tetraacrylate 2.81 Pentaerythritol monacrylate 1.21 Polycondensation product of 3-methoxy-diphenyl amine-4-diazonium sulfate and 4,4-bis-methoxy methyl diphenyl ether isolated as the mesitylene sulfonate 1.22 2-Stilbenyl-4,6-di(trichloromethyl)triazine 3.20 ~3~2g~
Methyl cellosolve~ 90.00 The coated and dried plate is exposed to actinic radiation through a negative exposure flat so as to yield seven solid steps on a 21 step Stouffer step wedge. The plate is developed using the following composition % w/w ~ 2-propoxy ethanol 14.85 - n-propanol 11.15 MgSO4 7H2O 8.00 NaH2PO4 (anhydrous) 1.50 Polyvinyl pyrrolidone * 1.50 Trycol OP-407 ** 0-75 polyethylene glycol 200 1.00 H2O Balance * MW = 10,000 ** nonyl phenol polyoxyethylene ethanol ~40 moles ethylene oxide) as a 70% solution in H2O.
and finished with the following composition ~ w/w Dextrin *** 5.52 sodium octyl sulfate 1.61 Triton X-100 **** 1.00 Givguard DXN ***** 0.05 3 4 2.37 H2O Balance ~ t~
~3~0294 *** hydrolyzed tapioca dextrin **** isooctyl phenol polyoxyethylene ethanol (4.5 moles ethylene oxide) ***** 2,5-dimethyl-6-acetoxy-dioxane and run on a Solna sheet fed press using abrasive ink, over-packing, and a Dahlgren dampening system until image breakdown is achieved. Under these conditions the plate provides 540,000 acceptable impressions.
Example 2 A lithographic printing plate is prepared and processed as described in Example 1 except that the pentaerythritol tetraacrylate is omitted. Under these conditions the plate provides only 180,000 acceptable impressions.
Example 3 A lithographic printing plate is prepared and processed as described in Example 1 except that the pentaerythritol mono-acrylate is omitted. Under these conditions the plate provides only 315,000 acceptable impressions.
Examp1e 4 A lithographic printing plate is prepared and processed as described in Example 1 except that the 2-stilbenyl-4,6-di-(trichloromethyl)triazine is omitted. Under these conditions the plate provides only 335,000 acceptable impressions.
It can be readily observed that plates prepared according to this invention (Example 1) show substantially increased press runs.
.
`` ~l3~294 4,4'-bis-methoxymethyl diphenyl ether, which is first precondensed with itself to form an oligomer having from 2 to 7 repeating units, and 3-methoxy-diphenylamine-4-diazonium sulphate.
Preferably, the diazonium salt comprises the 1:1 poly-condensation product of 3-methoxy-diphenylamine-4-diazonium - 4a -~3~9~
sulphate and 4,4'-bis-methoxymethyl, diphenyl ether, precipitated as the mesitylene sulfonate, such as is taught in United States 3,849,392.
The diazonium salt is preferably present in the composi-tion of the subject invention at a percent solids level of from about 3% to about 20% by weight. More preferably it is present at about 5% to about 18% by weight and most preferably the diazonium salt is present at a percent solids level of from about 10% to about 15% by weight.
The polymerizable mixture of the subject invention is comprised of , in admixture, a polyfunctional acrylic monomer which has from 3 to 6 unsaturated groups and a monofunctional acrylic monomer which has 1 unsaturated group.
The polyfunctional acrylic monomer is an ethylenically unsaturated compound having from three to six unsaturated groups and being capable of reacting with the monofunctional acrylic monomer upon exposure to imaging radiation. The polyfunctional monomer is characterized as having the unsaturated groups being acrylate or methacrylate esters. The preferred monomer is either a solid or liquid having a viscosity of greater than about 700mPa.S at 25C, preferably greater than about 2000mPa.s at 25C.
Most preferably, the monomer has a viscosity of greater than about 4000mPa.S at 25C.
Examples of compounds which are suitable for use as the polyfunctional acrylic monomer of this invention include trimethyl propane triacrylate and the ethoxylated or propoxylated homologs thereof, trimethylol propane tri-methacrylate and the ethoxylated ~3~Z~
or propoxylated analogs thereof, pentaerythritol triacrylate, pentaerythritol trimethacrylate, dipentaerythritol monohydroxy pentaacrylate, dipentaerythritol monohydroxy pentamethacrylate, dipentaerythritol hexaacrylate, dipentaerythritol hexamethacrylate, pentaerythritol tetraacrylate and pentaerythritol tetramethacry-late. Preferably, the monomer is pentaerythritol tetraacrylate, although a combination of suitable monomers is also advantageous.
The monofunctional monomer is an ethylenically unsaturated compound having one unsaturated group and is capable of reacting with the polyfunctional monomer upon exposure to imaging radiation. The monofunctional monomer is characterized as having the unsaturated group being an acrylate or methacrylate ester. Preferably, the monofunctional monomer is a liquid having a viscosity in the range of from about 1 to about 25 mPa.s at 25C.
Examples of compounds which are suitable for use as the monofunctional monomer of this invention include trimethylol : propane monoacrylate and the ethoxylated or propoxylated homologs thereof, trimethylol propane monomethacrylate and the ethoxylated or propoxylated homologs thereof, pentaerythritol acrylate, pentaerythritol methacrylate, tetrahydro furfuryl acrylate, tetrahydro furfuryl methacrylate, cyclohexyl acrylate, cyclohexyl methacrylate, n-hexyl acrylate, n-hexyl methacrylate, glycidyl acrylate and glycidyl methacrylate. Preferably, the monomer is : pentaerythritol monoacrylate, although a combination of suitable ~ monomers is also advantageous.
~3~D29~
In the polymerizable mixture of this invention the polyfunctional monomer should be present in an amount of more than at least about 50% and, more preferably, should be present in an amount of from about 65% to about 80%,based on the total weight of the monofunctional and polyfunctional monomers. The monofunctional monomer should comprise the balance of the poly-merizable mixture.
The polymerizable mixture is present at a percent solids level which is preferably in the range of from about 20% to about 70~ by weight. More preferably, the polymerizable mixture is present at a percent solids level of from about 30% to about 60%
by weight and most preferably from about 30% to about 50% by weight.
One of the advantages in having a polyfunctional monomer in the polymerizable mixture in combination with a monofunctional monomer is that the 3-dimensional structure provided by the polyfunctional monomer provides good matrix integrity allowing for a tough image and the linear propagation provided by the monofunctional monomer provides good photospeed. If the polymerizable mixture was comprised of two polyfunctional acrylic monomers, the resulting image would have good toughness but poor photospeed. If the mixture was comprised of two monofunctional acrylic monomers, there would be good photospeed but poor image toughness.
One of the significant aspects of this invention is that the unique combination of photoinitiator, diazonium salt and polymerizable mixture reduces the need for use of an oxygen 2~91 barrier layer or the necessity for processing in a nitroyen environment, although the exact mechanism for this is unclear.
Among the possible advantages derived thereby is elimination of 1) the inconvenience of applying a second coating, 2) the concern over the refractive index and solubility of the oxygen barrier layer, 3) the concern over blinding on a printing press due to residue from the oxygen barrier layer, and 4) the concern over potential image gain due to the oxygen barrier layer~
Other components which may be included in the radiation-polymerizable composition of this invention include acid stabilizers, exposure indicators, plasticizers, photoactivators and colorants.
Suitable acid stabilizers useful within the context ofthis invention include phosphoric, citric, benzoic, m-nitro benzoic, p(p-anilino phenylazo) benzene sulfonic acid, 4,4'-dini-tro-2,2'-stilbene disulfonic, itaconic, tartaric and p-toluene sulfonic acid, and mixtures thereof. Preferably, the acid stabilizer is phosphoric acid. When used, the acid stabilizer is preferably present in the radiation-polymerizable composition in the amount of from about 0.3% to about 2.0%, and most preferably from about 0.75% to about 1.5%, although the skilled artisan may use more or less as desired.
Exposure indicators (or photoimagers) which may be useful in conjunction with the present invention include 4-phenylazodiphenylamine, eosin, azobenzene, Calcozine Fuchsine~
dyes and Crystal Violet and Methylene Blue dyes. Preferably, the ~ r~
- ~3~029~
exposure indicator is 4-phenylazodiphenylamine. The exposure indicator, when one is used, is preferably present in the composition in an amount of from about 0.001% to about 0.035% by weight. A more preferred range is from about 0.002% to about 0.030% and, most preferably, the exposure indicator is present in an amount of from about 0.005% to about 0.20%, although the skilled artisan may use more or less as desired.
The photoactivator which may be included in the composition of this invention should be an amine-containing photoactivator which combines synergistically with the free-radical photoinitiator in order to extend the effective half-life of the photoinitiator, which is normally in the approximate range of about 10 9 to 10 15 seconds. Suitable photoactivators include 2-(n-butoxy) ethyl-4-dimethylamino benzoate, 2-(dimethylamino) amino benzoate and acrylated amines. Preferably the photoactivator is ethyl-4-dimethylamino benzoate. The photoactivator is preferably present in the composition of this invention in an amount of from about 1.0% to about 4.0% by weight, although the skilled artisan may use more or less as desired.
A plasticizer may also be included in the composition of this invention to prevent coating brittleness and to keep the composition pliable if desired. Suitable plasticizers include dibutylphthalate, triarylphosphate and, preferably, dioctylphathalate. The plasticizer is preferably present in the composition of this invention in an amount of from about 0.5% to about 1.25% by weight, although the skilled artisan may use more or less as desired.
Colorants useful herein include dyes such as Rhodamine, Calcozine, Victoria Blue and methyl violet, and such pigments as the anthraquinone and phthalocyanine types. Generally, the colorant is present in the form of a pigment dispersion which may comprise a mixture of one or more pigments and/or one or more dyes dispersed in a suitable solvent or mixture of solvents.
When a colorant is used, it is preferably present in the composition of this invention in an amount of from about 1.5% to about 4.0% by weight, more preferably from about 1.75% to about 3.0% and most preferably from about 2.0% to about 2.75%, although the skilled artisan may use more or less as desired.
In order to form a coating composition for the production of lithographic printing plates, the composition of this invention may be dispersed in admixture in a solvent or mixtureof solvents ; to facilitate application of the composition to the substrate.
Suitable solvents for this purpose include tetrahydrofuran, propylene glycol monomethyl ether, butyrolactone, methyl cellosolve, ethylene glycol ethers, alcohols such as ethyl 20 alcohol and n-propanol, and ketones such as methyl ethyl ketone, or mixtures thereof. Preferably, the solvent comprises a mixture of tetrahydrofuran, propylene glycol monomethyl ether and butyrolactone. In general, the solvent system is evaporated from the coating composition once it is applied to an appropriate substrate, however, some insignificant amount of solvent may remain as residue.
. .
. .
L3~29~L
~ ubstrates useful for coating with the composition of this invention to form a lighographic printing plate include sheets of transparent films such as polyester, aluminum and its alloys and other metals, silicon and similar materials which are well known in the art. Preferably, the substrate comprises aluminum. The substrate may first be pretreated by standard graining and/or etching and/or anodizing techniques as are well known in the art, and also may or may not have been treated with a composition such as polyvinyl phosphonic acid, sodium silicate or the like suitable for use as a hydrophilizing agent.
In the production of photographic elements such as lithographic printing plates, an aluminum substrate is first preferably grained by art recognized methods such as by means of a wire brush, a slurry of particulates or by chemical- or electrochemical means, for example in an electrolyte solution comprising hydrochloric acid. The grained plate is preferably then anodized for example in sulfuric or phosphoric acid in a manner well known in the art. The grained and anodized surface is preferably then rendered hydrophilic by treatment with poly-vinyl phosphonic acid by means which are also known to the skilledartisan. The thusly prepared plate is then coated with the composition of the present invention, preferably at a coating weight of from about 0.6g/m to about 2.5g/m , more preferably from about 0.8g/m to about 2.Og/m and most preferably from about 1.2g/m to about 1.5g/m , although these coa-ting weights are not critical to the practice of this invention, and dried.
~L3~)0~4 Preferably the thusly prepared lighographic printing plate is exposed to actinic radiation through a negative test flat so as to yield 6 solid steps on a 21 step Stouffer exposure wedge after development. The exposed plate is then developed with a suitable developer composition, preferably an organic solvent based developer, such as one compri.sing 2-propoxyethanol, a nonionic surfactant and an inorganic salt such as is disclosed in United States 4,308,340 and 4,381,340. In conventional use, the developed plate is finished with a subtractive finisher such as a hydrophllic polymer. Examples include cold water-soluble dextrin and/or polyvinyl pyrrolidone, a nonionic surfactant, a humectant, an inorganic salt and water, as taught by IJnited States 4,213,887.
For the purpose of improving the press performance of a plate prepared as described above, it is known that baking of the exposed and developed plate can result in an increase in the number of quality impressions over that otherwise obtainable. To properly bake the plate, it is first treated with a solution designed to prevent loss of hydrophilicity of the background during baking. An example of an effective solution is disclosed in United States 4,355,096. The thusly prepared plate is then heat treated by baXing at a temperature of from about 1~0C up to the annealing t-mperature of the substrate, most preferably about 240C. The effective baking time is inversely proportional to the temperature and averages in the range of from about 2 to ~.3~)0294 about 15 minutes. At 240C the time is about 7 minutes.
The following examples are illustrative of the invention but it is understood that the invention is not limited thereto.
None of the plates prepared in Examples 1-5 have an oxygen barrier layer thereon nor were they processed in a nitrogen environment.
Example 1 An 8" x 25" section of lithographic grade 1100 aluminum alloy is degreased with an aqueous alkaline degreasing solution and electrochemically grained using 900 coulombs of alternating current in an aqueous solution of nitric acid and aluminum nitrate.
The grained plate is well rinsed and anodized in a sulfuric acid bath wherein the aluminum is made anodic. Sufficient current and voltage is used to produce an oxide layer of 2.8g/m2. The anodized plate is well rinsed and hydrophilized by immersing the plate into a solution of polyvinyl phosphonic acid. The plate is well rinsed and dried. The thusly prepared plate is whirler coated with a solution having the following composition:
% w/w A terpolymer of polyvinyl acetate, polyvinyl alcohol and polyvinyl ~ormal commercially available as Formvar 12/85 4-54 Pentaerythritol tetraacrylate 2.81 Pentaerythritol monacrylate 1.21 Polycondensation product of 3-methoxy-diphenyl amine-4-diazonium sulfate and 4,4-bis-methoxy methyl diphenyl ether isolated as the mesitylene sulfonate 1.22 2-Stilbenyl-4,6-di(trichloromethyl)triazine 3.20 ~3~2g~
Methyl cellosolve~ 90.00 The coated and dried plate is exposed to actinic radiation through a negative exposure flat so as to yield seven solid steps on a 21 step Stouffer step wedge. The plate is developed using the following composition % w/w ~ 2-propoxy ethanol 14.85 - n-propanol 11.15 MgSO4 7H2O 8.00 NaH2PO4 (anhydrous) 1.50 Polyvinyl pyrrolidone * 1.50 Trycol OP-407 ** 0-75 polyethylene glycol 200 1.00 H2O Balance * MW = 10,000 ** nonyl phenol polyoxyethylene ethanol ~40 moles ethylene oxide) as a 70% solution in H2O.
and finished with the following composition ~ w/w Dextrin *** 5.52 sodium octyl sulfate 1.61 Triton X-100 **** 1.00 Givguard DXN ***** 0.05 3 4 2.37 H2O Balance ~ t~
~3~0294 *** hydrolyzed tapioca dextrin **** isooctyl phenol polyoxyethylene ethanol (4.5 moles ethylene oxide) ***** 2,5-dimethyl-6-acetoxy-dioxane and run on a Solna sheet fed press using abrasive ink, over-packing, and a Dahlgren dampening system until image breakdown is achieved. Under these conditions the plate provides 540,000 acceptable impressions.
Example 2 A lithographic printing plate is prepared and processed as described in Example 1 except that the pentaerythritol tetraacrylate is omitted. Under these conditions the plate provides only 180,000 acceptable impressions.
Example 3 A lithographic printing plate is prepared and processed as described in Example 1 except that the pentaerythritol mono-acrylate is omitted. Under these conditions the plate provides only 315,000 acceptable impressions.
Examp1e 4 A lithographic printing plate is prepared and processed as described in Example 1 except that the 2-stilbenyl-4,6-di-(trichloromethyl)triazine is omitted. Under these conditions the plate provides only 335,000 acceptable impressions.
It can be readily observed that plates prepared according to this invention (Example 1) show substantially increased press runs.
.
Claims (21)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A radiation-polymerizable composition comprising in admixture a) a polymeric binder;
b) a photoinitiator;
c) a diazonium salt; and d) a polymerizable mixture of i) a polyfunctional acrylic monomer having from 3 to 6 unsaturated groups; and ii) a monofunctional acrylic monomer having 1 unsaturated group.
b) a photoinitiator;
c) a diazonium salt; and d) a polymerizable mixture of i) a polyfunctional acrylic monomer having from 3 to 6 unsaturated groups; and ii) a monofunctional acrylic monomer having 1 unsaturated group.
2. The composition of claim 1 wherein said polyfunctional monomer is further characterized as having the unsaturated groups being acrylate or methacrylate esters.
3. The composition of claim 2 wherein said polyfunctional monomer is pentaerythritol tetraacrylate.
a, The composition of claim 1 wherein said monofunctional monomer is further characterized as having the unsaturated group be an acrylate or methacrylate ester.
5. The composition of claim 4 wherein said monofunctional monomer is pentaerythritol monoacrylate.
6. The composition of claim 1 wherein said polymerizable mixture is present in said composition in an amount of from about 20% to about 70% by weight.
7. The composition of claim 1 wherein said polyfunctional monomer is present in said polymerizable mixture in an amount more than about 50% by weight.
8. The composition of claim 7 wherein said polyfunctional monomer is present in said polymerizable mixture in an amount of from about 65% to about 80% by weight.
9. The composition of claim 1 wherein said monofunctional monomer is present in said polymerizable mixture in an amount of less than about 50% by weight.
10. The composition of claim 9 wherein said monofunctional monomer is present in said polymerizable mixture in an amount of from about 20% to about 35% by weight.
11. The composition of claim 1 wherein said polymeric binder is selected from the group consisting of epoxy resins, polyvinyl acetates, polyvinyl formals, polyvinyl butyrals, polyesters, polyamides, polyethers, polyurethanes and polyacrylic resins, and copolymers or terpolymers of any of these.
12. The composition of claim 11 wherein said polymeric binder comprises a terpolymer of polyvinyl acetate, polyvinyl alcohol and polyvinyl acetal.
13. The composition of claim 1 wherein said photoinitiator comprises a bis-trichloromethyl triazine having the formula Ar - CH = wherein Ar is and R1, R2, R3 and R4 are, independently, hydrogen, chlorine, bromine, alkoxy, or alkyl.
14. The composition of claim 13 wherein said photoinitiator is 2-stilbenyl-4,6-di(trichloromethyl)triazine.
15. The composition of claim 1 wherein said diazonium salt comprises the condensation product of 3-methoxy-diphenylamine-4-diazonium sulfate and 4,4'-bismethoxymethyl diphenyl ether.
16. The composition of claim 1 wherein said diazonium salt comprises the condensation product of 4,4'-bis-methoxymethyl diphenyl ether, which is first precondensed with itself to form an oligomer having from 2 to 7 repeating units, and 3-methoxy-diphenylamine-4-diazonium sulfate.
17. A photographic element comprising a substrate upon which the composition of claim 1 is coated.
18. The photographic element of claim 17 wherein said substrate is selected from the group consisting of aluminum and its alloys, polyester and silicon.
19. The photographic element comprising an aluminum contain-ing substrate upon which is coated a composition comprising in admixture a) a terpolymer of polyvinyl acetate, polyvinyl alcohol and polyvinyl formal;
b) 2-stilbenyl-4,6-di(trichloromethyl)triazine;
c) the condensation product of 3-methoxy-4-diazo-diphenylamine sulfate and 4,4'-bis-methoxymethyl diphenyl ether isolated as the mesitylene sulfonate;
and d) a polymerizable mixture of i) pentaerythritol tetraacrylate; and ii) pentaerythritol monoacrylate.
b) 2-stilbenyl-4,6-di(trichloromethyl)triazine;
c) the condensation product of 3-methoxy-4-diazo-diphenylamine sulfate and 4,4'-bis-methoxymethyl diphenyl ether isolated as the mesitylene sulfonate;
and d) a polymerizable mixture of i) pentaerythritol tetraacrylate; and ii) pentaerythritol monoacrylate.
20. A process for preparing and using a photographic element comprising combining in admixture a) a polymeric binder;
b) a photoinitiator;
c) a diazonium salt, and d) a polymerizable mixture of i) a polyfunctional acrylic monomer having from 3 to 6 unsaturated groups; and ii) a monofunctional acrylic monomer having 1 unsaturated group;
the process further comprising coating the composition formed by the mixture of a, b, c and d on a suitable substrate to form a photographic element; drying said mixture; imagewise exposing said element to actinic light and developing said element with a suitable developer.
b) a photoinitiator;
c) a diazonium salt, and d) a polymerizable mixture of i) a polyfunctional acrylic monomer having from 3 to 6 unsaturated groups; and ii) a monofunctional acrylic monomer having 1 unsaturated group;
the process further comprising coating the composition formed by the mixture of a, b, c and d on a suitable substrate to form a photographic element; drying said mixture; imagewise exposing said element to actinic light and developing said element with a suitable developer.
21. The process of claim 20 wherein said developer comprises 2-propoxyethanol.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US70711085A | 1985-02-28 | 1985-02-28 | |
| US707,110 | 1985-02-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1300294C true CA1300294C (en) | 1992-05-05 |
Family
ID=24840382
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000502905A Expired - Lifetime CA1300294C (en) | 1985-02-28 | 1986-02-27 | Radiation-polymerizable composition |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JPS61201234A (en) |
| CA (1) | CA1300294C (en) |
| DE (1) | DE3605717A1 (en) |
| GB (1) | GB2171713B (en) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3425328A1 (en) * | 1984-07-10 | 1986-01-16 | Hoechst Ag, 6230 Frankfurt | LIGHT SENSITIVE MIXTURE AND LIGHT SENSITIVE RECORDING MATERIAL MADE THEREOF |
| JPH0766186B2 (en) * | 1985-07-02 | 1995-07-19 | 富士写真フイルム株式会社 | Photosensitive composition |
| JPS62238553A (en) * | 1986-04-10 | 1987-10-19 | Nippon Foil Mfg Co Ltd | Photosensitive resin composition |
| JPS63194111A (en) * | 1987-02-06 | 1988-08-11 | Hitachi Ltd | Combustion method for gas fuel and equipment thereof |
| DE3738863A1 (en) * | 1987-11-16 | 1989-05-24 | Hoechst Ag | LIGHT-SENSITIVE PRINTING PLATE FOR WATERLESS OFFSET PRINTING |
| JPH04362350A (en) * | 1991-06-06 | 1992-12-15 | Kubota Corp | Transmission lubricating structure |
| US5466789A (en) * | 1992-01-21 | 1995-11-14 | Du Pont (Uk) Limited | Polyunsaturated diazonium compounds |
| GB2263906B (en) * | 1992-01-21 | 1995-11-08 | Du Pont | Improvements in or relating to polyunsaturated diazonium compounds |
| US5534623A (en) * | 1993-01-21 | 1996-07-09 | Du Pont (Uk) Limited | Process for preparing a polyunsaturated diazonium compounds |
| US5858615A (en) * | 1997-07-31 | 1999-01-12 | Morton International, Inc. | Hardenable photoimageable compositions |
| US6689489B2 (en) | 1999-10-07 | 2004-02-10 | Isg Technologies, Inc. | Composition for controlling spangle size, a coated steel product, and a coating method |
| WO2001027343A1 (en) | 1999-10-07 | 2001-04-19 | Bethlehem Steel Corporation | A coating composition for steel product, a coated steel product, and a steel product coating method |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL8001085A (en) * | 1979-02-27 | 1980-08-29 | Minnesota Mining & Mfg | PHOTOSENSITIVE MATERIALS AND OBJECTS. |
| DE3120052A1 (en) * | 1981-05-20 | 1982-12-09 | Hoechst Ag, 6000 Frankfurt | POLYMERIZABLE MIXTURE BY RADIATION AND COPYING MATERIAL MADE THEREOF |
-
1986
- 1986-02-22 DE DE19863605717 patent/DE3605717A1/en not_active Withdrawn
- 1986-02-27 JP JP4052286A patent/JPS61201234A/en active Pending
- 1986-02-27 GB GB08604818A patent/GB2171713B/en not_active Expired
- 1986-02-27 CA CA000502905A patent/CA1300294C/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61201234A (en) | 1986-09-05 |
| GB2171713A (en) | 1986-09-03 |
| GB8604818D0 (en) | 1986-04-03 |
| GB2171713B (en) | 1988-05-25 |
| DE3605717A1 (en) | 1986-08-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4772538A (en) | Water developable lithographic composition | |
| US4940646A (en) | Polyvinyl acetal with hydroxy aliphatic acetal groups useful in photosensitive negative working compositions | |
| US4877711A (en) | Light-sensitive diazo photopolymerizable composition with polyurethane having carbon-carbon unsaturated and a carboxyl group | |
| US4659645A (en) | Photosensitive mixture and photosensitive recording material with diazonium salt polycondensation product and free radical radiation polymerizable composition | |
| AU604815B2 (en) | Improved recording material | |
| CA1300294C (en) | Radiation-polymerizable composition | |
| US4511640A (en) | Aqueous developable diazo lithographic printing plates with admixture of polyvinyl acetate and styrene maleic acid ester copolymer | |
| US4652604A (en) | Radiation-polymerizable composition and element containing a photopolymer composition | |
| JPH0232293B2 (en) | ||
| US4806450A (en) | Photosensitive photopolymerizable recording element having a terpolymer binder in the photopolymerizable layer | |
| JP2736124B2 (en) | Photopolymerizable recording material | |
| US20030166750A1 (en) | Method for the production of anhydride modified polyvinyl acetals useful for photosensitive compositions | |
| CA1276048C (en) | Polyvinyl acetal resin and photosensitive composition containing same | |
| US5238772A (en) | Photopolymerizable mixture and recording material containing free-radically polymerizable compound, photosensitive polymerization initiator and polyurethane binder grafted with vinyl alcohol and vinyl acetal units | |
| US4618562A (en) | Aqueous developable lithographic printing plates containing an admixture of diazonium salts and polymers and composition therefor | |
| US4839254A (en) | Photosensitive mixture and photosensitive recording material produced therefrom with polymeric binder which is reaction product of (thio) phosphinic acidiso (thio) cyanate and active hydrogen containing polymer | |
| CA1267478A (en) | Radiation-polymerizable composition | |
| US4895788A (en) | Water developable lithographic composition | |
| US4946373A (en) | Radiation-polymerizable composition | |
| US4851319A (en) | Radiation polymerizable composition, photographic element, and method of making element with diazonium salt, and monofunctional and polyfunctional acrylic monomers | |
| US5242779A (en) | Photosensitive mixture containing photocurable compound and polyurethane binder with grafted vinyl alcohol units, carboxylic acid vinyl ester units and vinyl acetal units | |
| US5134053A (en) | Graft polymer with unsaturated lateral chains, photosensitive mixture containing said graft polymer and recording material produced therefrom | |
| US4780392A (en) | Radiation-polymerizable composition and element containing a photopolymerizable acrylic monomer | |
| US4707437A (en) | Radiation-polymerizable composition and element containing a photopolymer composition | |
| US4539285A (en) | Photosensitive negative diazo composition with two acrylic polymers for photolithography |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKLA | Lapsed |