US2754279A - Aqueous composition of an unmodified hydroxyl-containing resinous glycidyl polyether of a dihydric phenol - Google Patents

Aqueous composition of an unmodified hydroxyl-containing resinous glycidyl polyether of a dihydric phenol Download PDF

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US2754279A
US2754279A US239841A US23984151A US2754279A US 2754279 A US2754279 A US 2754279A US 239841 A US239841 A US 239841A US 23984151 A US23984151 A US 23984151A US 2754279 A US2754279 A US 2754279A
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water
plate
resin
image
developer
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US239841A
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Myron W Hall
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3M Co
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Minnesota Mining and Manufacturing Co
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Priority to US239841A priority Critical patent/US2754279A/en
Priority to GB19818/56A priority patent/GB799102A/en
Priority to FR1154744D priority patent/FR1154744A/en
Priority to DEM30971A priority patent/DE1192667B/en
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    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/26Processing photosensitive materials; Apparatus therefor
    • G03F7/30Imagewise removal using liquid means
    • G03F7/32Liquid compositions therefor, e.g. developers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/02Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
    • C08J3/09Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
    • C08J3/091Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids characterised by the chemical constitution of the organic liquid
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2363/00Characterised by the use of epoxy resins; Derivatives of epoxy resins

Description

United States Patent Ofice 2,754,279 Patented July 10, 1956 AQUEOUS COMPOSITION OF AN UNMODIFIED HYDRGXYL-CONTAINTNG RESENGUS GLYZ- IDYL POLYETIER F A DEIYDRI PHENOL Myron W. Hall, St. Paul, Minn., assignor to Minnesota Mining & Manufacturing Company, St. Paul, Minrn, a corporation of Delaware N0 Drawing. Application August 1, 1951, Serial No. 239,841
5 Claims. (Cl. 26ll-29.2)
This invention relates to developers.
In one common form of planographic printing, a water-soluble light-sensitive coating on a grained metal plate is exposed to light through a suitable stencil or negative to insolubilize the exposed portion, and the unexposed portion of the coating is later washed away, leaving a hydrophobic image on a hydrophilic plate. Albumen sensitized with bichromate provides a typical water-soluble light-sensitive coating. After exposure, the plate is commonly lightly coated with developingink, which adheres over the entire coating. The plate is then wiped dry. Washing the plate with water then removes the soluble portions of the coating, together with the developing-ink adhering thereto, leaving the inked and therefore readily visible insolubilized exposed image portion in place ready for printing by the lithographic method.
In an alternative procedure, employing a more recently developed type of planographic printing-plate such as will be further identified hereinbelovv, the plate is washed immediately after exposure to remove the soluble portions of the coating and leave the substantially invisible insolubilized image portion in condition for printing. Application of printing ink, as in a lithographic press, then renders the image visible. However, it is preferred, as. in the. earlier procedure described above, to'develo'p the image to a visible state prior to placing the plate on the press, so that the operator can determine whether or not he has a good plate, and so that the plate may be correctly positioned on the press. The present invention supplies an improved developer composition for such applications.
While the novel developer of the present invention is entirely efiective on dichromate-albumen type printing plates, it is particularly Well adapted for use with presensitized planographic printing plates, particularly such as are described in 'the co-pending application of .Tewett and Case, Serial No. 199,566, filed December 6, 1950. Such plates employ extremely thin diazo resin lightsensitive coatings. The thinness of the coating requires that the unexposed areas be removed prior to application of printing ink or other developer. Application of prior art developing-inks to the resulting plate prior to placing on the press is unsatisfactory. Unless extreme precautions are taken in applying the ink to the image, some of the ink frequently adheres to image-free areas of the. plate, particularly in half-tone areas. The ink offers no protection against wear when the press is in operation. Other priorart developers, protective asphalt solutions, etc., have also shown a tendency to, adhere to areas of the plate other than the image areas, or have been affected by the oils of the ink employed on the press, or have not adequately protected the original image from mechanical abrasion and Wear, or have been unsatisfactory in a number of these or other respects.
A primary object of the present invention is therefore to provide a developer for exposed pre-sensitized planoplanographic printing-plate 2 7 graphic printing plates which overcomes the difi'iculties experienced with prior art developers. A particular object is to provide a developer applicable to the developing of plates such as are described in the above-identified Jewett et al. application, especially after removal of the unexposed portions of the pre-sensitized coating. Another object is to provide a developer capable of producing a visible image of increased thickness and improved wear-resistance. such a developer in permanently readily applicable form. A further object is to provide a developed printing-plate having greatly increased press life as well as improved inking and printing qualities. Other objects and advantages will be made apparent as the description proceeds.
Specific exemplary formulas of image-developers made in accordance with the invention and having the desired properties will now be supplied, for purposes of explanation but not of limitation. In these formulas, parts are given as parts by weight unless otherwise noted.
Example 1 Aqueous phase: Parts Water 25 gum arabic solution in Water 18, Wetting agent (sodium lauryl sulfate; may be omitted if desired) l.8 Non-aqueous phase:
Ethylene dichloride 60 Cyclohexanone 40 Soft epoxy resin 30 Pigment (toluidine toner) 9 The resin employed was an epichlorohydrin-bisphenol (epoxy) resin stated to have a melting point of 40 C., epoxide equivalent of 300475, hydroxy equivalent of 1 05, and was very viscous but still fluid at normal room temperatures.
The pigment, resin, and about eight parts of the cyclohexanone were combined on a paint mill, and the resulting mixture was then dispersed in the mixed remaining solvents in a churn. Combining the aqueous and nonaqueous phases in a mixer then produced a water-in-oil type emulsion of high viscosity, which ,did not separate even on prolonged standing. Applied to an exposed and washed lithographic plate, this developer provided a clearly visible image with no bridging of half-tone dots.
Example 2 Aqueous phaseas in Example 1.
Non-aqueous phase-as in Example 1 with the exception that a normally hard, brittle, rosin-like epoxy resin was substituted for the soft resin of Example 1. This hard resin was stated to have a melting point of C.,' epoxide equivalent of 9G5 985, and hydroxy equivalent of 175.
Mixing the two solutions produced a Water-in-oil type emulsion which did not separate. Used as a developer, the emulsion provided clear images with no bridging of half-tones. The. developed image was extremely Wear: resistant 0n the press, and in this respect was even better than that produced with the emulsion of Example 1, par-. ticularly at elevated temperatures.
Example 3 Aqueous phase-as in Example 1.
A non separating water-in-oil type emulsion was produced by milling together the resin, pigment, and 10 Another object is to providev parts of cyclohexanone, dissolving the mixture in the remaining solvents, and then mixing the liquid blend with the aqueous phase in a high-speed mixer.
Example 4 Example 5 Aqueous phase: Parts Water 112 25% gum arabic solution in water 23 Sodium lauryl sulfate 2.3
Non-aqueous phasei Ethylene dichloride"; 6O Epoxy resin of Example 2 30 T oluidine toner 9 The resulting emulsion was of the oilin water type. Lithographic images were satisfactorily developed with this emulsion, particularly at somewhat below normal room temperatures.
Example 6 v Aqueous phase -as in Example 1.
Non-aqueous phaseas in Example 5 except that trichloroethane was substituted for ethylene dichloride.
As in Example 1, a water-in-oil emulsion was obtained. Some bridging of half-tone dots was noted when this emulsion was used in developing half-tone lithographic plates. Line drawings and the like were satisfactorily developed. After developing the plates, they were preferably allowed to stand for an hour or more, or briefly heated, in order to remove any stickiness caused by solvent retention in the resin coating.
Example 7 Aqueous phaseas in Example 1.
Non-aqueous phase:
Ethylene dichloride 6O Epoxy resin as in Example l 30 Toluidine toner 6 An oil-in-water type emulsion was obtained, which was equally as effective as the emulsion of Example 5 as a lithographic plate developer. V
In the-application of these developers to diazo sensi-' tizedprinting-plates suchas those described in the aboveidentified Jewett et al. application, the following pro-- cedure has been found eifective.
The pro-sensitized plate is first exposed to light through a stencil or negative, an exposure of 2-4 minutes-at 24 inches from a 35-ampere carbon are being suitable. After exposure the plate is desensitized by wipingwith water containing a small amount of gum arabic, to dissolve and remove the unexposed and unreacted soluble portion of the diazo sensitizer. At this point the remaining exposed image portion is substantially invisible. While the plate is still wet with the gum'arabic solution, a quantity of the developer, e. g. as specified in Example 1 hereinabove, is poured on the plate and wiped over the image-area-with a soft pad or cotton wad until the image is uniformly coated. The same action eifectively re-dissolves and removes any portion of the developer resin which may temporarily adhere to non-image areas of the plate such as the areas between half-tone dots. As soon asthe image is completely coated, and before any further deposition of resin can occur, the excess developer'is rinsedfrom the plate by flooding with water. The plate is then ready to be placed on the press. Alternatively, the developed plate may be coated with a protective layer of gum arabic solution, wiped dry, and stored for future reference. The color imparted by the developer makes it possible for the operator readily to determine the perfection of the hydrophobic image areas.
In the printing operation, after the plate has been installed on a lithographic press, the gum arabic coating, if present, is first removed by sponging with water or with a weak fountain solution. The fountain rollers should be dropped first and, after a few revolutions of the press, the ink rollers may be dropped. The image should ink up quickly. No special inks or fountain solutions are required, and most materials commonly used for this purpose will be found to be satisfactory. A typical lithographic ink contains suitable colored pigments dispersed in a rapid-drying liquid vehicle having a drying-oil base. In order to obtain the maximum number of satisfactory impressions, the press should be carefully adjusted to the least pressure consistent with quality printing. The image may at intervals be re-developed and further protected from wear on the press by repeated applications of the developer.
The epoxy resins, as indicated by the foregoing examples, are well adapted for use in my novel lithographic plate developer emulsions. They are insoluble in water. They are soluble in suitable volatile organic solvents, from which they may be recovered in the form of strong tough films. They adhere firmly to the image portions of the plate to provide a surface which is desirably organophilic and ink-receptive without being soluble in, or otherwise objectionably aifected by, the ink. The epoxy resin developed surface has excellent wear-resistance, which is particularly important with lithographic plates having extremely thin image layers such as the diazo-resin-coated plates of the aforementioned Jewett et a1. invention.
The epoxy resins are produced by reacting together certain polyhydric phenolic bodies, of which bis-phenol (p,p'-dihydroxydiphenyl dimethyl methane) is a typical example, with polyfunctional alcohol-contributing reactants such as epichlorhydrin, the extent of reaction and hence the molecular weight of the product being determined by the ratio of the principal reactants and/orby the introduction of controlled small amounts of suitable monofunctional short-stop, materials such as phenol or ethylene chlorhydrln. The resulting resin may be considered a polymeric polyhydric alcohol, and as such is capable of further reaction, e. g. with drying oil fatty acids, resin acids, acid anhydrides, aldehydes, etc.; and such reaction products inmany instances are applicable as components of image-developers in accordance with this invention. These various epoxy resins, including derivatives as. just described, are preferred by me as components of my novel developer compositions, although other equivalent resins andresinous materials are not thereby to be considered as excluded. 7 V
A further example will now be provided of a developer composition which has given excellent results when properly appliedand treated, but is somewhat less desirable from e standpointof rapidity of application than are the preceding compositions.
f Example 8' Aqueous phase-as in Example 1. Non-aqueous phase:
Solution of melamine formaldehyde 4 butanol resin Xylol 45 Toluidine toner 9 Mixing the two solutions duced a water-in-oiltypeemulsion, which was applied to an exposed and washed lithographic plate as a developer. Theresin adheredwell to the image, but remained too soft forprolonged effective press operation until cured position and degree of.
in a high-speed mixer pro-' overnight at room temperature or for minutes at 260 F. After curing, the plate was found to have excellent press life.
The resin solution consisted of 65 parts of resin dissolved in 35 parts of xylol. Resimine No. 882 is a typical example of such a resin solution available commercially at the filing date of this application. In preparing such a resin, melamine is catalytically condensed with greater than an equal mol proportion of formaldehyde in the presence of butyl alcohol, which also largely enters into the reaction. Xylol is ordinarily present both to control the viscosity and as an aid in the removal of water.
The properties of the particular resins employed are thus seen to be highly important to the successful operation of the lithographic plate developers of my invention. However, the applicability and utility of these novel developer compositions does not depend solely on the properties of the resin employed. The solvent or solvent mixture, the pigment or other coloring agent, the water-soluble components, the proportions of these several materials, and other factors are all significant to the successful attainment of the objects of this invention, as will be further pointed out.
Ethylene dichloride is an effective water-immiscible volatile solvent for epoxy resins. Solutions of resin in this solvent are readily emulsified with an aqueous phase. The resin solution is a good solvent for additional resin such as may be accidentally deposited on non-image portions of the plate during the developing operation. Ethylene dichloride evaporates rapidly so that the developed plate is immediately ready for the press. As shown by Examples 5 and 7, ethylene dichloride may be used as the sole resin solvent. Trichloroethane is also an effective water-immiscible volatile solvent for epoxy resins, having somewhat lower volatility than ethylene dichloride.
While ethylene dichloride or the like, used alone, provides useful results, I have found that the addition of a further volatile solvent, e. g. cyclohexanone, provides still further improvement in the image-developing characteristics of the compositions of my invention. Cyclohexanone is soluble in water and, if used as the sole resin solvent, causes the deposition of a thin scum over the entire plate area. However, when cyclohexanone or other equivalent volatile and water-miscible solvent is added to ethylene dichloride, as in Examples 1-4 hereof, there is, surprisingly, even less of a tendency towards scum formation than occurs when ethylene dichloride is employed alone.
The concentration of resin in the solvent or solvent mixture may be widely varied. At excessive dilution, it will be apparent that prolonged treatment will be required in order to develop an adequately visible and wear-resistant coating, and hence I prefer to include at least about 30 parts of resin for each 100-150 parts of solvent. Too high a concentration, however, may cause curdling of the emulsion, and such viscous solutions are also more likely to form strings and thus cause bridging of halftone dots and smearing of non-image areas. For example reducing the ethylene dichloride content of Example 1 to much less than about parts has been found to cause curdling of the emulsion and bridging of the half-tones. I therefore prefer to use an amount of water-immiscible solvent at least about equal to the amount of resin.
The presence of both an aqueous and a non-aqueous or oily phase in the developer as applied to the exposed and washed plate in processes such as hereinabove described is found to be highly desirable in the proper development of the image. Application of a resin solution in the absence of the aqueous phase, for example, results in deposition of resin over substantially the entire plate area. Such a resin solution may eifectively be applied to a bichromate-albumen type plate, where the unexposed portion of the sensitized coating is ordinarily not removed until after the application of the developer; and in this method of application the concentration of the resin may be widely varied. Even for such applications, however,
6 the pre-formed emulsion is found to. have a number of advantages.
Surprisingly, it has been observed that both the waterin-oil and the oil-in -water type emulsions are effective in developing lithographic plates, and particularly for plates prepared in accordance with the above-referred-to Jewett et al. application. In either case, the resin solution is selectively adsorbed at the image areas and is prevented from being adsorbed at the non-image areas of the plate; or, if some of the resin accidentally becomes deposited on such non-image areas, due for example, to excessive drying out of the material in localized areas, it is quicklyre-dissolved and removed by other portions of the solution during the rubbing or swabbing operations incident to development.
It has also been observed that the oil-in-water type emulsions are more easily applied to the plate, since, as previously pointed out, the latter is first covered with an aqueous gum solution; and the oil-in-water emulsion is immediately and uniformly miscible therewith. The presence of a wetting agent is usually desirable, although not essential, in securing an oil-in-Water type emulsion as well as in obtaining improved wetting action on the plate. In some instances the oil-in-water emulsions have separated into two layers on standing, a phenomenon which has not been observed with my water-in-oil emulsions. However, this separation may be retarded by increasing the proportion of water-soluble gum, or by other means; and in any event is not a serious disadvantage, since the two phases are readily re-combined and emulsified by brief stirring or shaking.
Examples have been provided of two specific pigments; many others are equally applicable. Soluble dyes, such as DuPont Oil Red may also be employed, although the developed image then ordinarily has less depth of color than is obtainable with pigments. The pigment or other coloring agent need not necessarily be combined with the resin components in the developer composition, although such combination is ordinarily preferred. When the pigment of Example 1 was omitted from the non-aqueous phase and introduced instead into the aqueons phase, the emulsion was of the oil-in-water type. On application as a lithographic plate developer, the pigment was taken up by the resin coating on the image areas, producing a colored image.
Gum arabic is widely employed in the lithographic printing art and hence is suggested here also. However other water-soluble gums are known which are fully or substantially equivalent to gum arabic for such operations, and substitution of such materials is considered as coming fully within the scope of this invention. Sodium carboxymethyl cellulose is one such water-soluble thickener. Likewise, the sodium lauryl sulfate of the foregoing examples may be efiectively replaced by soap or various other Wetting agents; and entirely satisfactory compositions have also been produced in which no Wetting agents were used, or in which additional water-soluble gum replaced part or all of the wetting agent. In this connection, it has been observed that amine type wetting agents, e. g. triethanolamine oleate, have a tendency to cause the deposition of an adherent scum or residue over the entire plate; and these materials are therefore to be avoided.
This invention provides, in the lithographic printing art, a new and simplified method of obtaining visible printing-plate images, accurate inking and printing, and increased Wear-resistance of the image, through application of a novel lithographic plate developer composition as herein above described and illustrated. The composition and application is particularly advantageous with lithographic plates of the type described in the Jewett et al. application Serial No. 199,566, wherein developing is carried out after the non-exposed portions of the pre-sensitized layer have been removed. The res'ulting developed plates are superior to prior art plates, particularly as to wear-resistance.
-What is claimed is as follows:
1. A lithographic printing-plate image developer comprising a colored two-phase liquid composition having an aqueous phase comprising Water and a soluble thickener, and a non-aqueous liquid resinous phase comprising an unmodified hydroxyl-containing resinous glycidyl polyether of a dihydric phenol, and a water-immiscible volatile solvent.
2. A lithographic printing-plate image developer comprising a colored two-phase liquid composition having an internal aqueous phase comprising water and a soluble thickener, and an external non-aqueous liquid resinous phase comprising an unmodified hydroxyl-containing resinous glycidyl polyether of a dihydric phenol, and a water-immiscible volatile solvent.
3'. A lithographic printing-plate image developer comprising a colored two-phase liquid composition having an external aqueous phase comprising water, a Wetting agent and a soluble thickener, and an internal non-aqueous liquid resinous phase comprising an unmodified hydroxyl-containing resinous glycidyl polyether of a dihydric phenol, and a water-immiscible volatile solvent.
. 4. A lithographic printing-plate image developer comprising a colored two-phase liquid composition having an aqueous phase comprising water and a soluble thickener, and a non-aqueous liquid resinous phase comprister-miscible solvent, of an'unmodifie d hydroxyl-contain-Q ing resinous glycidyl polyether of a dihydric phenol.
References Cited in the file of this patent UNI'ITEDV STATES PATENTS 1,032,890 Fritsche "July 16, 1912 2,345,447 Bassist Mar. 28, 1944 2,364,692 Cassel Dec. 12, 1944 2,441,653 Van Dusen May 18, 1948 2,448,749 Van Dusen Sept. 7, 1943 2,467,186 Cairns Apr. 12, 1949 2,637,621 Auer j May 5,
1953 OTHER REFERENCES Paint, on & Chem; Review, vol. 113, No. 23, pages 1548, 48 and 49, November 9, 1950. V

Claims (1)

1. A LITHOGRAPHIC PRINTING-PLATE IMAGE DEVELOPER COMPRISING A COLORED TWO-PHASE LIQUID COMPOSITION HAVING AN AQUEOUS PHASE COMPRISING WATER AND A SOLUBLE THICKENER, AND A NON-AQUEOUS LIQUID RESINOUS PHASE COMPRISING AN UNMODIFIED HYDROXYL-CONTAINING RESINOUS GLYCIDYL POLYETHER OF A DIHYDRIC PHENOL, AND A WATER-IMMISCIBLE VOLATILE SOLVENT.
US239841A 1951-08-01 1951-08-01 Aqueous composition of an unmodified hydroxyl-containing resinous glycidyl polyether of a dihydric phenol Expired - Lifetime US2754279A (en)

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Application Number Priority Date Filing Date Title
US239841A US2754279A (en) 1951-08-01 1951-08-01 Aqueous composition of an unmodified hydroxyl-containing resinous glycidyl polyether of a dihydric phenol
GB19818/56A GB799102A (en) 1951-08-01 1956-06-26 Improvements in planographic printing plate developers
FR1154744D FR1154744A (en) 1951-08-01 1956-06-29 Aqueous composition based on hydroxylated polyether glycidyl, stable and resinous, derived from a diphenol
DEM30971A DE1192667B (en) 1951-08-01 1956-06-30 Composition and process for making visible, strengthening and protective coating of the exposed image areas of a lithographic printing plate

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US239841A US2754279A (en) 1951-08-01 1951-08-01 Aqueous composition of an unmodified hydroxyl-containing resinous glycidyl polyether of a dihydric phenol
GB19818/56A GB799102A (en) 1951-08-01 1956-06-26 Improvements in planographic printing plate developers

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US2865873A (en) * 1957-02-06 1958-12-23 Litho Chemical And Supply Co I Lacquer emulsion for lithographic plates
US2872428A (en) * 1955-01-31 1959-02-03 Shell Dev Polyepoxide emulsions and method of treating textiles therewith
US2872427A (en) * 1954-10-04 1959-02-03 Shell Dev Polyepoxide emulsions and method of treating textiles therewith
US2994609A (en) * 1956-09-25 1961-08-01 Azoplate Corp Development of diazotype printing plates
US3010389A (en) * 1953-03-09 1961-11-28 Buskes Willem Marie Photographic transfer printing plates
US3010390A (en) * 1954-06-29 1961-11-28 Buskes Willem Marie Planographic printing plates
US3010391A (en) * 1954-06-29 1961-11-28 Grinten Chem L V D Light-sensitive sheets and process for producing transfer images
US3019105A (en) * 1957-02-28 1962-01-30 Harris Intertype Corp Treatment of diazo-sensitized lithographic plates
US3091533A (en) * 1958-05-22 1963-05-28 Developer composition for a light
US3113866A (en) * 1957-01-22 1963-12-10 Polaroid Corp Photographic processes and compositions useful therein
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US3136637A (en) * 1958-11-26 1964-06-09 Minnesota Mining & Mfg Presensitized lithographic light-sensitive sheet construction
US3158476A (en) * 1961-01-13 1964-11-24 Azoplate Corp Process for the improvement of fixed electrophotographic printing plates which are water-conductive in the image-free parts
US3161518A (en) * 1957-11-01 1964-12-15 Lithoplate Inc Diazo sensitized lithographic plate comprising a hydrophilic amine formaldehyde intermediate layer
US3351008A (en) * 1965-12-06 1967-11-07 Dick Co Ab Composition for treatment of imaged lithographic masters and method of use
US3378372A (en) * 1963-05-02 1968-04-16 Gevaert Photo Prod Nv Durability of offset printing plates
US3390992A (en) * 1964-06-15 1968-07-02 North American Rockwell Non-etching circuit fabrication
US3455688A (en) * 1966-02-10 1969-07-15 Riddet Co Lacquer emulsion for presensitized lithographic plates
US3481740A (en) * 1964-01-30 1969-12-02 Summer Williams Inc Emulsion developers for lithographic plates
US3511654A (en) * 1964-12-30 1970-05-12 Keuffel & Esser Co Reprographic process
DE1622743B1 (en) * 1961-03-30 1971-06-03 Agfa Ag Process for the production of planographic printing forms with an aluminum base
US3615791A (en) * 1966-10-24 1971-10-26 Lithoplate Inc Lacquer emulsions for lithographic plates and method for their manufacture
WO1987007735A1 (en) * 1986-06-09 1987-12-17 Imperial Metal & Chemical Company Additive developer
US4786580A (en) * 1983-12-27 1988-11-22 Hoechst Celanese Corporation Method of developing imaged diazo material with propanol containing developer composition
US5154994A (en) * 1988-10-06 1992-10-13 Fujitsu Limited Method of and apparatus for forming volume type phase hologram
US5176986A (en) * 1989-03-17 1993-01-05 Basf Aktiengesellschaft Liquid cleaner composition for removing polymeric materials from a surface
US20030064319A1 (en) * 2001-05-21 2003-04-03 Tokyo Ohka Kogyo Co., Ltd. Negative photoresist compositions for the formation of thick films, photoresist films and methods of forming bumps using the same

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US2448749A (en) * 1947-01-24 1948-09-07 Addressograph Multigraph Treated planographic printing plate
US2467186A (en) * 1945-04-20 1949-04-12 Du Pont Aqueous dispersions of synthetic linear polyamide and process for obtaining same
US2637621A (en) * 1949-05-02 1953-05-05 Auer Laszlo Textile decorating pigment color composition containing a phenolepihalohydrin condensation product

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US2448749A (en) * 1947-01-24 1948-09-07 Addressograph Multigraph Treated planographic printing plate
US2637621A (en) * 1949-05-02 1953-05-05 Auer Laszlo Textile decorating pigment color composition containing a phenolepihalohydrin condensation product

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US3010389A (en) * 1953-03-09 1961-11-28 Buskes Willem Marie Photographic transfer printing plates
US3010390A (en) * 1954-06-29 1961-11-28 Buskes Willem Marie Planographic printing plates
US3010391A (en) * 1954-06-29 1961-11-28 Grinten Chem L V D Light-sensitive sheets and process for producing transfer images
US2872427A (en) * 1954-10-04 1959-02-03 Shell Dev Polyepoxide emulsions and method of treating textiles therewith
US2872428A (en) * 1955-01-31 1959-02-03 Shell Dev Polyepoxide emulsions and method of treating textiles therewith
US2994609A (en) * 1956-09-25 1961-08-01 Azoplate Corp Development of diazotype printing plates
US3113866A (en) * 1957-01-22 1963-12-10 Polaroid Corp Photographic processes and compositions useful therein
US2865873A (en) * 1957-02-06 1958-12-23 Litho Chemical And Supply Co I Lacquer emulsion for lithographic plates
US3019105A (en) * 1957-02-28 1962-01-30 Harris Intertype Corp Treatment of diazo-sensitized lithographic plates
US3161518A (en) * 1957-11-01 1964-12-15 Lithoplate Inc Diazo sensitized lithographic plate comprising a hydrophilic amine formaldehyde intermediate layer
US3091533A (en) * 1958-05-22 1963-05-28 Developer composition for a light
DE1166002B (en) * 1958-07-04 1964-03-19 Algraphy Ltd Process for developing photolithographic plates
US3136637A (en) * 1958-11-26 1964-06-09 Minnesota Mining & Mfg Presensitized lithographic light-sensitive sheet construction
US3158476A (en) * 1961-01-13 1964-11-24 Azoplate Corp Process for the improvement of fixed electrophotographic printing plates which are water-conductive in the image-free parts
DE1622743B1 (en) * 1961-03-30 1971-06-03 Agfa Ag Process for the production of planographic printing forms with an aluminum base
US3378372A (en) * 1963-05-02 1968-04-16 Gevaert Photo Prod Nv Durability of offset printing plates
US3481740A (en) * 1964-01-30 1969-12-02 Summer Williams Inc Emulsion developers for lithographic plates
US3390992A (en) * 1964-06-15 1968-07-02 North American Rockwell Non-etching circuit fabrication
US3511654A (en) * 1964-12-30 1970-05-12 Keuffel & Esser Co Reprographic process
US3351008A (en) * 1965-12-06 1967-11-07 Dick Co Ab Composition for treatment of imaged lithographic masters and method of use
US3455688A (en) * 1966-02-10 1969-07-15 Riddet Co Lacquer emulsion for presensitized lithographic plates
US3615791A (en) * 1966-10-24 1971-10-26 Lithoplate Inc Lacquer emulsions for lithographic plates and method for their manufacture
US4786580A (en) * 1983-12-27 1988-11-22 Hoechst Celanese Corporation Method of developing imaged diazo material with propanol containing developer composition
US4714670A (en) * 1986-06-09 1987-12-22 Imperial Metal & Chemical Company Developer including an aliphatic cyclic carbonate in the oil phase emulsion
WO1987007735A1 (en) * 1986-06-09 1987-12-17 Imperial Metal & Chemical Company Additive developer
US5154994A (en) * 1988-10-06 1992-10-13 Fujitsu Limited Method of and apparatus for forming volume type phase hologram
US5176986A (en) * 1989-03-17 1993-01-05 Basf Aktiengesellschaft Liquid cleaner composition for removing polymeric materials from a surface
US20030064319A1 (en) * 2001-05-21 2003-04-03 Tokyo Ohka Kogyo Co., Ltd. Negative photoresist compositions for the formation of thick films, photoresist films and methods of forming bumps using the same
US20060035169A1 (en) * 2001-05-21 2006-02-16 Tokyo Ohka Kogyo Co., Ltd. Negative photoresist compositions for the formation of thick films, photoresist films and methods of forming bumps using the same
US20060035170A1 (en) * 2001-05-21 2006-02-16 Koji Saito Negative photoresist compositions for the formation of thick films, photoresist films and methods of forming bumps using the same
US7063934B2 (en) * 2001-05-21 2006-06-20 Toyko Ohka Kogyo Co., Ltd. Negative photoresist compositions for the formation of thick films, photoresist films and methods of forming bumps using the same
US7129018B2 (en) 2001-05-21 2006-10-31 Toyko Ohka Kogyo Co., Ltd. Negative photoresist compositions for the formation of thick films, photoresist films and methods of forming bumps using the same
US7419769B2 (en) 2001-05-21 2008-09-02 Tokyo Ohka Kogyo Co., Ltd. Negative photoresist compositions for the formation of thick films, photoresist films and methods of forming bumps using the same

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FR1154744A (en) 1958-04-16
GB799102A (en) 1958-07-30

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