US2763553A - Lithographic offset printing process - Google Patents
Lithographic offset printing process Download PDFInfo
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- US2763553A US2763553A US267482A US26748252A US2763553A US 2763553 A US2763553 A US 2763553A US 267482 A US267482 A US 267482A US 26748252 A US26748252 A US 26748252A US 2763553 A US2763553 A US 2763553A
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/06—Silver salts
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03B—APPARATUS OR ARRANGEMENTS FOR TAKING PHOTOGRAPHS OR FOR PROJECTING OR VIEWING THEM; APPARATUS OR ARRANGEMENTS EMPLOYING ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ACCESSORIES THEREFOR
- G03B15/00—Special procedures for taking photographs; Apparatus therefor
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/29—Development processes or agents therefor
- G03C5/315—Tanning development
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S101/00—Printing
- Y10S101/29—Printing involving a color-forming phenomenon
Definitions
- LITHOGRAPHIC OFFSET PRINTING PROCESS Filed Jan. 21. 1952 EXPOSURE 9 ⁇ /6 UNHARDENED x LYN.WWN XWP EMULSION TANMNGDE'VELOP/NGAGE'NT DEVELOPMENT IN ALKALINE $0LU770/V HARDENED HYMOP/l/UC COLLOID-P/GMHVT Jv HEA 77/V6 mArvsFimw 5TRA7Z/M' w/Mr RECEPT/VE PR/NT/NG PAPE Walier Clark IffbQf/B. Cowden I N V EN TORS ATTY.
- This invention relates to methods for preparing lithographic oifset printing plates and particularly to methods for preparing such plates having a paper base.
- Lithographic paper printing plates have been prepared and used in a similar manner. That is, a paper sheet may be provided with a hydrophilic surface and the ink-receptive image is applied to the surface in a well-known manner.
- the ink-receptive image can be de veloped in a light-sensitive colloid layer on the treated surface of the paper plate as described above.
- our invention contemplates forming in a substantially unhardened gelatino-silver halide emulsion layer, hardened image areas corresponding to the highlights of a subject and other coplanar areas which are not hardened and which correspond to the shadows of the subject, then transferring a stratum of the unhardened areas to a hydrophilic surface which will repel greasy printing inks when wetted during lithographic printing operations.
- suitable hydrophilic surf-aces to which the stratum adheres in preference to the hardened areas of the emulsion can be mentioned fibrous cellulosic surfaces such as present on wood, paper and cloth; grained zinc, anodized aluminum, surfaces of hydrophilic organic colloid such as surface hydrolyzed cellulose ester e. g. a. surface hydrolyzed cellulose acetate sheet, surface hydrolyzed synthetic resins such as surface hydrolyzed polyvinyl acetate, polyvinyl alcohol, gelatin, casein, pigmented gelatin or casein etc.
- the balance of our process includes treating the transferred stratum of gelatin emulsion on the hydrophilic surface so as to increase its ink receptivity and decrease its moisture absorbing properties, and then using the resulting printing plate in a lithographic printing press to obtain lithographic prints.
- Preferred embodiments of our invention involve making the transfer of the stratum unhardened emulsion to the surface of pigmented hydrophilic colloid layers.
- dry pigmentcoated paper such as a paper coated with a mixture of gelatin and baryta, for example, ordinary baryta-coated photographic paper, and after heating the transferred colloid image, or other treatment to render the transferred colloid ink-receptive, a moderately durable printing plate results.
- the pigmented paper can be coated with a thin layer of organic colloid material such as gum arabic and the transfer made to the dried sheet.
- organic colloid material such as gum arabic
- press endurance is reduced since the transferred. image adheres less readily to the unpigmented organic colloid surface.
- Further improvement is obtained if the pigment-colloid coated sheet is hardened more than is normally possible during the pigmentcolloid coating operation, by treatment of the pigmented paper with an oxidizing solution such as an acid dichromate solution containing tannic acid.
- a lithographic printing element which includes a paper base which has been rendered Water-repellent and which has been coated with a mixture of hardened hydrophilic organic colloid material and inert pigment.
- a paper base which has been rendered Water-repellent and which has been coated with a mixture of hardened hydrophilic organic colloid material and inert pigment.
- Suitable for this purpose is a paper which has been coated with a mixture of well-hardened casein and a pigment such as clay, barium sulfate, etc. If the casein-coated'paper is provided with a 'layer containing gelatin and pigment, it may be treated as above to render the surface less absorptive.
- Figs. l 'to 4 illustrate in greatly enlarged cross-sectional view representative materials and methods used in preparing a lithographic .printing plate according to our invention.
- Example 1 A lithographic printing element having a hydrophilic surface is prepared by coating a melamine-formaldehyde sized paper stock of medium weight with a mixture of gelatin and baryta containing a gelatin hardening agent such as formaldehyde or aluminum chloride. The baryta coating is then hardened by application of 1.7 grams of the following solution per square foot of surface followed by'drying:
- An unhardened paper stock is coated with a substantially unhardened gelatino-silver halide emulsion preferably containing a substantially water-insoluble gelatin tanning developing agent such as 3,4-dihydroxy diphenyl, 2,5-dihydroxy diphenyl or 2,3-dihydroxy diphenyl and prepared by the methods described in the Yackel U. S. patent application Serial No. 783,912, filed November 4, 1947, now U. S. Patent 2,592,368, grantedApril 8, 1952.
- Water-soluble tanning developing agents such as hydroquinone or pyrocatechol are less preferred but can be utilized in the emulsion.
- the emulsion is not harder than a gelatin layer containing 0.7 gram of formaldehyde per pound of gelatin freshly coated.
- the silver halide sensitized sheet is then exposed by projection or contact printing methods under a two-tone subject such as a line or halftone transparency or printed matter. If desired, reflex exposure methods may be used for making the exposure.
- the exposure procedure is illustrated in Fig. 1 of the drawings, wherein the silver halide sensitized element having the paper, film, or other support carrying the unhardened emulsion layer 11 is shown undergoing exposure to light under the subject comprising a transparent or semi-transparent support 12 carrying a line or halftone image 13 such as present on printed matter on paper. Exposure produces latent images principally in areas 14 of emulsion 11, the remaining areas receiving little or no exposure unless it is desired to impart optical density to those areas to facilitate inspection of those areas subsequently.
- the exposed element is then developed as described in the Yutzy et al invention by treating the exposed emulsion with a minimum of alkaline solution such as 3 percent aqueous sodium carbonate solution which may contain a softening agent such as urea, etc., for about 20 to 45 seconds at room temperature.
- alkaline solution such as 3 percent aqueous sodium carbonate solution which may contain a softening agent such as urea, etc.
- the result as shown in Fig. 2 of the drawings, is to develop the exposed silver halide and tan or harden the gelatin in areas 15 of the emulsion layer 11, the remaining unexposed areas 16 containing unhardened emulsion.
- the excess alkaline solution is then squeegeed from the surface of the emulsion layer.
- the pigmented hardened hydrophiliccolloid surface of the baryta-coated paper prepared as above is then pressed against the surface of the developed emulsion :layer :11, taking reasonable care to prevent excessive light exposure of the emulsion layer, and very soon 'thereafteris peeled off.
- the printing element to dry heat suflicient to improve ink-receptivity and preferably at a temperature below the charring point of the transferred colloid stratum; that is, a temperature of the order of 150 to 275 C. for ten seconds to three minutes, depending upon the temperature used and the extent to which theelement has been dried before heating. At 230 to 250 C., 20 seconds is satisfactory for a previously dried element or -seconds if the element is moist from the transfer operation.
- the finalprinting plate is then obtained having the structure shown in Fig. 4 of the drawings wherein areas 19 are the inkv receptive portions of the printing plate and the remaining surface of layer 18 is hydrophilic and Will absorb sufficient moisture in the lithographic printing press to repel the greasy printing ink.
- the printing plate may then be used directly in a lithographic printing press; however, improved results are obtained if, prior to inking, the plate is next treated with a solution of a bi-valent metal salt such as zinc acetate and/or application of an aqueous solution of glycerin and phosphoric acid.
- a bi-valent metal salt such as zinc acetate and/or application of an aqueous solution of glycerin and phosphoric acid.
- Other metal salts which are satisfactory are disclosed in the Worthen U. S. Patent 2,534,650 granted December 19, 1950, and suitable acidic glycerin solutions are disclosed in the Van Dusen U. S. Patent 2,515,536, granted July 18, 1950.
- Example 2 A sized paper stock of medium weight is rendered water-repellent by coating a casein solution on theface side so as to obtain about .15-.6 gram .of casein per square foot of surface as follows:
- a normal baryta coating is then applied to the casein coating from a composition containing one part of gelatin per 10 parts of barium sulfate and formaldehyde as the hardener for the gelatin. The coating is applied so as to obtain three grams of solid per square foot. Subsequently the baryta coating is further hardened by treatment with the acid dichromate solution of Example 1 using 1.7 grams of solution per square foot of surface.
- An unhardened paper stock is then coated with a substantially unhardened gelatino-silver halide emulsion layer preferably containing a silver halide tanning developing agent as described in Example 1.
- This sensitive element is then exposed to the desired subject and developed in alkaline solution.
- the casein and baryta-coated printing element prepared above is then pressed against the developed emulsion layer under reduced illumination and quickly peeled off.
- the hardened image areas do not adhere to the baryta coated surface whereas the unexposed, undeveloped and unhardened areas adhere, and a stratum thereof comes off on to the'p'igmented hydrophilic surface of the printing element.
- the element now carrying the adhered stratum is then heated underthe conditions set forth in Example 1.
- the printing plate Prior to inking the printing plate in the lithographic printing press, it may be treated with the mentions 1. salt and glycerin solutions if desired.
- the printing plate shows little distortion in the printing press in the presence of moisture and press endurance is high since the printing areas adhere well to the baryta coating.
- Example 3 As the hydrophilic lithographic printing element a sized paper support is provided carrying a layer of a mixture of a hardened organic colloid such as casein and an inert pigment such as clay or baryta, and if desired, treated with a cuprammonium solution or a salt solution such as zinc acetate before, after, or during application to the caseinpigment coat of a thin coating of a hydrophilic colloid such as sodium alginate as described in U. S. Patent 2,534,650 granted December 19, 1950.
- the coated surface of this element is then pressed against the moistened surface of the sensitive element which has been exposed and processed as mentioned in the previous examples, followed by separation of the two sheets and heating the printing element carrying the adhered emulsion stratum.
- the resulting printing plate is used directly in a lithographic printing press, treating it if desired with the solutons indicated in Example 1 prior to inking the plate.
- Our invention contemplates the use of other treatments besides heat, zinc salts, etc. set forth in Example 1, for increasing the ink-receptivity of the transferred colloid image on the hydrophilic surface.
- a hardening agent for gelatin such as formaldehyde, alum, etc.
- Another very convenient and useful method involves making the transfer of the unhardened emulsion stratum, as above described, to the hydrophilic surfaces mentioned, then merely (further exposure is not necessary) treating it with an alkali solution.
- the stratum contains undeveloped silver halide, developing agent and gelatin, apparently the result is to develop the silver halide and at the same time tan the gelatin with the oxidation products of the developing agent.
- a 520% sodium carbonate solution is satisfactory, employed for about 30 seconds at about 70-85 F., followed by an acid rinse such as 1-2% acetic acid, or rinsing with Water.
- acid rinse such as 1-2% acetic acid, or rinsing with Water.
- Other alkaline solutions may be used with similar results such as those containing trlsodium phosphate, alkali metal hydroxides, sodium metaborate etc.
- Patent 2,716,059 granted August 23, 1955, we may employ a mixture of gelatin tanning and non-tanning developing agents in the emulsion layer such as a mixture of preferably 35-40% of one of the indicated dihydroxy diphenyl tanning developing agents, and 4-methoxy-1-naphthol or p-hydroxyanilino-methane sulfonic acid, etc., non-tanning developing agents.
- the silver halide emulsion may be of the usual negative type or may be a direct positive emulsion.
- the pigment used in the coating of the hydrophilic printing element may be any of the well known inert pigments, particularly inert mineral pigments such as clay, barium sulfate, titanium oxide, etc., and carbon black, although it is preferred to use light-colored pigments to obtain maximum contrast to light between the inked image and the hydrophilic surface of the printing plate.
- the hydrophilic colloid of the pigmented printing element can be gelatin or casein, as indicated, or other organic colloids such as polyvinyl alcohol, gum arabic, starch, albumin, methyl cellulose, cellulose sulfate, partially hydrolyzed polyvinyl acetate, zein, etc., particularly those materials which can be insolubilized and hardened most readily, particularly with the bi-valent metal salts and yet retain hydrophilic properties.
- the hydrophilic surfaces to which the emulsion transfer is made can be any of the grained metal surfaces such as of grained zinc and anodized aluminum.
- the organic colloid material used as in Example 3 to render the paper support moisture-repellent may consist of any of the well known water-resistant materials such as synthetic resins, cellulose esters, rubber, etc., applied from solvent or aqueous dispersions, such as methyl meth acrylate resin, cellulose acetate, natural or artificial rubber latex.
- the organic colloid component of the pigmented layer should be selected so as to obtain optimum adherence to the water-repellent layer and to this end subbing layers may be interposed between the pigmented hydrophilic colloid layer and the moisture-repellant layer. It is not necessary but may be advisable in some cases to coat the paper base on both sides with the water-repellent organic colloid material such as hardened casein.
- a method for preparing a lithographic printing plate which comprises pressing the hydrophilic surface of a supported layer containing a mixture of hardened gelatin and an inert pigment, against a moistened supported substantially unhardened gelatino-silver halide emulsion layer which has been exposed to a two-tone subject and developed in the presence of a mixture of gelatin tanning and non-tanning silver halide developing agents producing hardened image areas which will not adhere to said hydrophilic surface and other coplanar areas corresponding to the shadows of the subject which adhere to said hydrophiiic surface, said emulsion layer being not harder than a gelatin layer containing 0.7 gram of formaldehyde per pound of gelatin freshly coated, mechanically removing the support of said emulsion layer together with the hardened image areas from the hydrophilic surface to leave a stratum of only said coplanar emulsion areas containing gelatin tanning silver halide developing agent adhered to said surface, and then treating said hydrophilic surface with an alka
Description
ii' 1956 w. CLARK ET AL 2,763,553
LITHOGRAPHIC OFFSET PRINTING PROCESS Filed Jan. 21. 1952 EXPOSURE 9 {/6 UNHARDENED x LYN.WWN XWP EMULSION TANMNGDE'VELOP/NGAGE'NT DEVELOPMENT IN ALKALINE $0LU770/V HARDENED HYMOP/l/UC COLLOID-P/GMHVT Jv HEA 77/V6 mArvsFimw 5TRA7Z/M' w/Mr RECEPT/VE PR/NT/NG PAPE Walier Clark IffbQf/B. Cowden I N V EN TORS ATTY. & Ae'r United States Patent LITHOGRAPHIC OFFSET PRINTING PROCESS Walter Clark and Herbert B. Cowden, Rochester, N. Y., assignors to Eastman Kodak Company, Rochester, N. Y., a corporation of New Jersey Application January 21, 1952, Serial No. 267,482
1 Claim. (Cl. 95-5.4)
This invention relates to methods for preparing lithographic oifset printing plates and particularly to methods for preparing such plates having a paper base.
There are a number of Well-known methods for preparing lithographic oifset printing plates. Perhaps the most common method involves sensitizing a metal plate, such as a zinc plate which has been grained, with a light-sensitive coating such as bichromated albumin following which the plate is exposed usually to a line or halftone negative and before developing the plate a coating of lithographic developing ink is applied. Subsequently the plate is developed in water to remove the albumin in the unexposed areas leaving the hardened albumin covered with ink in the exposed regions. When the plate is moistened and then inked with a greasy printing ink in the lithographic printing press, the ink is taken up only in the areas occupied by the hardened albumin image. If it is necessary to reverse the image, actually this can be accomplished in the usual manner by first transferring the ink image to a rubber oifset blanket and thence to the paper, otherwise the ink image can be transferred directly from the printing plate to the receiving paper.
Lithographic paper printing plates have been prepared and used in a similar manner. That is, a paper sheet may be provided with a hydrophilic surface and the ink-receptive image is applied to the surface in a well-known manner. For example, the ink-receptive image can be de veloped in a light-sensitive colloid layer on the treated surface of the paper plate as described above. These methods possess the obvious disadvantages that during the development of the ink-receptive image, it is difficult to remove all of the unhardened colloid in the unexposed region which is intended to repel the greasy printing ink when moistened. Moreover, in the development of such paper plates with aqueous solutions, a certain amount of distortion of the plate occurs which is obviously undesirable.
We have discovered a process which overcomes the disadvantages of previously known methods for preparing lithographic printing plates. Our process involves exposure to a subject, of a substantially unhardened silver halide emulsion layer, followed by tanning development of the emulsion and transfer of the unexposed areas to a suitably-prepared absorbent hydrophilic surface. Subsequently the transferred colloid image is heated or given other treatment to render it more fully receptive of greasy printing inks, and the resultant product used directly in a lithographic printing press in the usual manner.
In the Yutzy and Yackel U. S. patent application Serial No. 783,914, filed November 4, 1947, now U. S. patent 2,596,756, granted May 13, 1952, is described a photographic reproduction method which involves the steps of exposing a substantially unhardened silver halide emulsion layer, preferably containing a tanning developing agent, followed by development of the emulsion layer under conditions of tanning development and then transferring a stratum only of the unhardened areas of the emul- 2,763,553 Patented Sept. 18, 1956 sion layer to a suitable absorbent hydrophilic surface such as paper, cloth or wood.
We have discovered that the basic principles of that process can be utilized for forming a lithographic printing plate. That is, we have found that the stratum of emulsion which has been transferred to the absorbent hydrophilic surface can be inked with greasy printing inks and used for making lithographic prints, particularly if the stratum is further treated to render it more fully selectively receptive of printing ink when the element is moistened and inked in the press. Accordingly, our invention contemplates forming in a substantially unhardened gelatino-silver halide emulsion layer, hardened image areas corresponding to the highlights of a subject and other coplanar areas which are not hardened and which correspond to the shadows of the subject, then transferring a stratum of the unhardened areas to a hydrophilic surface which will repel greasy printing inks when wetted during lithographic printing operations. As examples of suitable hydrophilic surf-aces to which the stratum adheres in preference to the hardened areas of the emulsion, can be mentioned fibrous cellulosic surfaces such as present on wood, paper and cloth; grained zinc, anodized aluminum, surfaces of hydrophilic organic colloid such as surface hydrolyzed cellulose ester e. g. a. surface hydrolyzed cellulose acetate sheet, surface hydrolyzed synthetic resins such as surface hydrolyzed polyvinyl acetate, polyvinyl alcohol, gelatin, casein, pigmented gelatin or casein etc.
The balance of our process includes treating the transferred stratum of gelatin emulsion on the hydrophilic surface so as to increase its ink receptivity and decrease its moisture absorbing properties, and then using the resulting printing plate in a lithographic printing press to obtain lithographic prints.
Several methods are available for treating the transferred stratum of emulsion to increase its ink receptivity as will be apparent from consideration of the examples thereinafter, such as drying and heating.
Preferred embodiments of our invention involve making the transfer of the stratum unhardened emulsion to the surface of pigmented hydrophilic colloid layers. We have found that useful results are obtained if we make the transfer of the unhardened colloid image to dry pigmentcoated paper such as a paper coated with a mixture of gelatin and baryta, for example, ordinary baryta-coated photographic paper, and after heating the transferred colloid image, or other treatment to render the transferred colloid ink-receptive, a moderately durable printing plate results. In order to obtain a printing plate of better quality, it is desirable to decrease the moisture absorption properties of the pigment-coated paper. This can be accomplished by moistening the pigmented surface prior to making the transfer but this operation increases the transfer time and the image tends to smear. Alternately, the pigmented paper can be coated with a thin layer of organic colloid material such as gum arabic and the transfer made to the dried sheet. However, in this case press endurance is reduced since the transferred. image adheres less readily to the unpigmented organic colloid surface. Further improvement is obtained if the pigment-colloid coated sheet is hardened more than is normally possible during the pigmentcolloid coating operation, by treatment of the pigmented paper with an oxidizing solution such as an acid dichromate solution containing tannic acid.
In a preferred method a lithographic printing element is provided which includes a paper base which has been rendered Water-repellent and which has been coated with a mixture of hardened hydrophilic organic colloid material and inert pigment. Suitable for this purpose is a paper which has been coated with a mixture of well-hardened casein and a pigment such as clay, barium sulfate, etc. If the casein-coated'paper is provided with a 'layer containing gelatin and pigment, it may be treated as above to render the surface less absorptive.
In the accompanying drawings, Figs. l 'to 4 illustrate in greatly enlarged cross-sectional view representative materials and methods used in preparing a lithographic .printing plate according to our invention.
The following examples are provided to illustrate representative methods for carrying out our invention.
Example 1 A lithographic printing element having a hydrophilic surface is prepared by coating a melamine-formaldehyde sized paper stock of medium weight with a mixture of gelatin and baryta containing a gelatin hardening agent such as formaldehyde or aluminum chloride. The baryta coating is then hardened by application of 1.7 grams of the following solution per square foot of surface followed by'drying:
Water cc 295 Hydrochloric acid (0.05 gm. per cc.) cc 64 Potassium dichromate grams 4 Tannic acid (0.05 gram per cc.) ce 32 Saponin (7.5% aqueous sol.) cc 5 The printing element prepared as just described has the structure of the element shown in Fig. 3 of the accompanying drawings wherein layer 17 is the paper support to which is attached the hardened baryta coating 18.
An unhardened paper stock is coated with a substantially unhardened gelatino-silver halide emulsion preferably containing a substantially water-insoluble gelatin tanning developing agent such as 3,4-dihydroxy diphenyl, 2,5-dihydroxy diphenyl or 2,3-dihydroxy diphenyl and prepared by the methods described in the Yackel U. S. patent application Serial No. 783,912, filed November 4, 1947, now U. S. Patent 2,592,368, grantedApril 8, 1952. Water-soluble tanning developing agents such as hydroquinone or pyrocatechol are less preferred but can be utilized in the emulsion. The emulsion is not harder than a gelatin layer containing 0.7 gram of formaldehyde per pound of gelatin freshly coated. The silver halide sensitized sheet is then exposed by projection or contact printing methods under a two-tone subject such as a line or halftone transparency or printed matter. If desired, reflex exposure methods may be used for making the exposure. The exposure procedure is illustrated in Fig. 1 of the drawings, wherein the silver halide sensitized element having the paper, film, or other support carrying the unhardened emulsion layer 11 is shown undergoing exposure to light under the subject comprising a transparent or semi-transparent support 12 carrying a line or halftone image 13 such as present on printed matter on paper. Exposure produces latent images principally in areas 14 of emulsion 11, the remaining areas receiving little or no exposure unless it is desired to impart optical density to those areas to facilitate inspection of those areas subsequently.
The exposed element is then developed as described in the Yutzy et al invention by treating the exposed emulsion with a minimum of alkaline solution such as 3 percent aqueous sodium carbonate solution which may contain a softening agent such as urea, etc., for about 20 to 45 seconds at room temperature. The result, as shown in Fig. 2 of the drawings, is to develop the exposed silver halide and tan or harden the gelatin in areas 15 of the emulsion layer 11, the remaining unexposed areas 16 containing unhardened emulsion. The excess alkaline solution is then squeegeed from the surface of the emulsion layer.
As shown in Fig. 3 of the drawings, the pigmented hardened hydrophiliccolloid surface of the baryta-coated paper prepared as aboveis then pressed against the surface of the developed emulsion :layer :11, taking reasonable care to prevent excessive light exposure of the emulsion layer, and very soon 'thereafteris peeled off. Since the emulsion layer 11 contains-the hardened image areas 15 which will not adhere to the hardened hydrophilic surface of layer 18, and other coplanar unhardened areas 16 which will adhere to layer 18, when the layer 18 is peeled off a stratum of area =16.adheres to it. Even at this stage the printing element carrying the adhered area 16 is useful as a lithographic printing plate. If it is dried down before use .in the printing press, it is found that While areas 16 are still more hydrophilic than desired, these areas will selectively attract printing inks when moistened and prints can be obtained therefrom. Accordingly, at this stage in order to render those areas more fully ink-receptive, we subject the printing element to dry heat suflicient to improve ink-receptivity and preferably at a temperature below the charring point of the transferred colloid stratum; that is, a temperature of the order of 150 to 275 C. for ten seconds to three minutes, depending upon the temperature used and the extent to which theelement has been dried before heating. At 230 to 250 C., 20 seconds is satisfactory for a previously dried element or -seconds if the element is moist from the transfer operation. At 150 (3., three minutes and .at 275 C., 10 seconds heating are required. The finalprinting plate is then obtained having the structure shown in Fig. 4 of the drawings wherein areas 19 are the inkv receptive portions of the printing plate and the remaining surface of layer 18 is hydrophilic and Will absorb sufficient moisture in the lithographic printing press to repel the greasy printing ink. The printing plate may then be used directly in a lithographic printing press; however, improved results are obtained if, prior to inking, the plate is next treated with a solution of a bi-valent metal salt such as zinc acetate and/or application of an aqueous solution of glycerin and phosphoric acid. Other metal salts which are satisfactory are disclosed in the Worthen U. S. Patent 2,534,650 granted December 19, 1950, and suitable acidic glycerin solutions are disclosed in the Van Dusen U. S. Patent 2,515,536, granted July 18, 1950.
Example 2 A sized paper stock of medium weight is rendered water-repellent by coating a casein solution on theface side so as to obtain about .15-.6 gram .of casein per square foot of surface as follows:
To 800 gms. casein in water is added sufficient aqueous ammonia solution to obtain pH=9.0. After filtering,'the solution is neutralized :to pH=6.5 with citric acid. This solution is then diluted with 120 F. water to a 7% casein solution. Spreading agent and 11 cc. of 20% formaldehyde solution per gms. of casein are then added and coatings are made directly from this solution. A normal baryta coating is then applied to the casein coating from a composition containing one part of gelatin per 10 parts of barium sulfate and formaldehyde as the hardener for the gelatin. The coating is applied so as to obtain three grams of solid per square foot. Subsequently the baryta coating is further hardened by treatment with the acid dichromate solution of Example 1 using 1.7 grams of solution per square foot of surface.
An unhardened paper stock is then coated with a substantially unhardened gelatino-silver halide emulsion layer preferably containing a silver halide tanning developing agent as described in Example 1. This sensitive element is then exposed to the desired subject and developed in alkaline solution. The casein and baryta-coated printing element prepared above is then pressed against the developed emulsion layer under reduced illumination and quickly peeled off. As before, the hardened image areas do not adhere to the baryta coated surface whereas the unexposed, undeveloped and unhardened areas adhere, and a stratum thereof comes off on to the'p'igmented hydrophilic surface of the printing element. The element now carrying the adhered stratum is then heated underthe conditions set forth in Example 1. Prior to inking the printing plate in the lithographic printing press, it may be treated with the mentions 1. salt and glycerin solutions if desired. As a result of using the casein-coated paper stock as a support for the baryta layer, the printing plate shows little distortion in the printing press in the presence of moisture and press endurance is high since the printing areas adhere well to the baryta coating.
Example 3 As the hydrophilic lithographic printing element a sized paper support is provided carrying a layer of a mixture of a hardened organic colloid such as casein and an inert pigment such as clay or baryta, and if desired, treated with a cuprammonium solution or a salt solution such as zinc acetate before, after, or during application to the caseinpigment coat of a thin coating of a hydrophilic colloid such as sodium alginate as described in U. S. Patent 2,534,650 granted December 19, 1950. The coated surface of this element is then pressed against the moistened surface of the sensitive element which has been exposed and processed as mentioned in the previous examples, followed by separation of the two sheets and heating the printing element carrying the adhered emulsion stratum. The resulting printing plate is used directly in a lithographic printing press, treating it if desired with the solutons indicated in Example 1 prior to inking the plate.
Our invention contemplates the use of other treatments besides heat, zinc salts, etc. set forth in Example 1, for increasing the ink-receptivity of the transferred colloid image on the hydrophilic surface. To this end we can obtain very satisfactory results by treating the gelatin emulsion image With a hardening agent for gelatin such as formaldehyde, alum, etc. Another very convenient and useful method involves making the transfer of the unhardened emulsion stratum, as above described, to the hydrophilic surfaces mentioned, then merely (further exposure is not necessary) treating it with an alkali solution. Since the stratum contains undeveloped silver halide, developing agent and gelatin, apparently the result is to develop the silver halide and at the same time tan the gelatin with the oxidation products of the developing agent. For this purpose a 520% sodium carbonate solution is satisfactory, employed for about 30 seconds at about 70-85 F., followed by an acid rinse such as 1-2% acetic acid, or rinsing with Water. Other alkaline solutions may be used with similar results such as those containing trlsodium phosphate, alkali metal hydroxides, sodium metaborate etc.
A number of other variations may be made in our methods for preparing printing plates which fall within the scope of our invention. We may use light-sensitive elements disclosed in the Yackel invention mentioned, containing the developing agent in the emulsion or not. In the latter case a soluble silver halide tanning developing agent is employed in the alkaline developing solution used to effect tanning development. Also, as described in the Yutzy et a1. U. S. patent application Serial No. 267,447, filed concurrently herewith, now U. S. Patent 2,716,059, granted August 23, 1955, we may employ a mixture of gelatin tanning and non-tanning developing agents in the emulsion layer such as a mixture of preferably 35-40% of one of the indicated dihydroxy diphenyl tanning developing agents, and 4-methoxy-1-naphthol or p-hydroxyanilino-methane sulfonic acid, etc., non-tanning developing agents. The silver halide emulsion may be of the usual negative type or may be a direct positive emulsion. The pigment used in the coating of the hydrophilic printing element may be any of the well known inert pigments, particularly inert mineral pigments such as clay, barium sulfate, titanium oxide, etc., and carbon black, although it is preferred to use light-colored pigments to obtain maximum contrast to light between the inked image and the hydrophilic surface of the printing plate. The hydrophilic colloid of the pigmented printing element can be gelatin or casein, as indicated, or other organic colloids such as polyvinyl alcohol, gum arabic, starch, albumin, methyl cellulose, cellulose sulfate, partially hydrolyzed polyvinyl acetate, zein, etc., particularly those materials which can be insolubilized and hardened most readily, particularly with the bi-valent metal salts and yet retain hydrophilic properties. As mentioned, the hydrophilic surfaces to which the emulsion transfer is made can be any of the grained metal surfaces such as of grained zinc and anodized aluminum.
The organic colloid material used as in Example 3 to render the paper support moisture-repellent may consist of any of the well known water-resistant materials such as synthetic resins, cellulose esters, rubber, etc., applied from solvent or aqueous dispersions, such as methyl meth acrylate resin, cellulose acetate, natural or artificial rubber latex. The organic colloid component of the pigmented layer should be selected so as to obtain optimum adherence to the water-repellent layer and to this end subbing layers may be interposed between the pigmented hydrophilic colloid layer and the moisture-repellant layer. It is not necessary but may be advisable in some cases to coat the paper base on both sides with the water-repellent organic colloid material such as hardened casein.
What we claim is:
A method for preparing a lithographic printing plate which comprises pressing the hydrophilic surface of a supported layer containing a mixture of hardened gelatin and an inert pigment, against a moistened supported substantially unhardened gelatino-silver halide emulsion layer which has been exposed to a two-tone subject and developed in the presence of a mixture of gelatin tanning and non-tanning silver halide developing agents producing hardened image areas which will not adhere to said hydrophilic surface and other coplanar areas corresponding to the shadows of the subject which adhere to said hydrophiiic surface, said emulsion layer being not harder than a gelatin layer containing 0.7 gram of formaldehyde per pound of gelatin freshly coated, mechanically removing the support of said emulsion layer together with the hardened image areas from the hydrophilic surface to leave a stratum of only said coplanar emulsion areas containing gelatin tanning silver halide developing agent adhered to said surface, and then treating said hydrophilic surface with an alkaline solution to develop the silver halide of the adhered stratum and at the same time tan the gelatin thereof with the oxidation products of the developing agent.
References Cited in the file of this patent UNITED STATES PATENTS 1,618,505 Beebe Feb. 22, 1927 1,892,682 Richards Jan. 3, 1933 2,058,396 Baker Oct. 27, 1936 2,184,310 Meigs .1. Dec. 26, 1939 2,214,565 Montgomery et al Sept. 10, 1940 2,484,431 Staehle Oct. 11, 1949 2,534,650 Worthen Dec. 19, 1950 2,549,177 Davidson Apr. 17, 1951 2,568,503 Kenyon et a1 Sept. 18, 1951 2,596,756 Yutzey et al May 13, 1951 2,716,059 Yutzy et al Aug. 23, 1955
Priority Applications (18)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE485609D BE485609A (en) | 1947-11-04 | 1942-10-30 | |
US783912A US2592368A (en) | 1947-11-04 | 1947-11-04 | Gelatine silver halide emulsion layer containing a dihydroxy diphenyl tanning developing agent |
US783914A US2596756A (en) | 1947-11-04 | 1947-11-04 | Photomechanical copy method |
GB10545/48A GB655274A (en) | 1947-11-04 | 1948-04-15 | Improvements in processes of photographic reproduction |
GB10544/48A GB655273A (en) | 1947-11-04 | 1948-04-15 | Improved photographic materials |
BE485611D BE485611A (en) | 1947-11-04 | 1948-10-30 | |
FR980399D FR980399A (en) | 1947-11-04 | 1948-11-03 | New photosensitive products and process for the preparation of reliefs on these products |
FR980401D FR980401A (en) | 1947-11-04 | 1948-11-03 | Improved process for transferring photographic images and resulting products |
DEE2141A DE874704C (en) | 1947-11-04 | 1950-09-17 | Light-sensitive layer for drawing canvas |
US267482A US2763553A (en) | 1947-11-04 | 1952-01-21 | Lithographic offset printing process |
US267446A US2675313A (en) | 1947-11-04 | 1952-01-21 | Photographic reproduction process |
DEE6633A DE927307C (en) | 1947-11-04 | 1953-01-20 | Process for the photographic reproduction of pamphlets or the like. |
FR1089934D FR1089934A (en) | 1947-11-04 | 1953-01-21 | Photographic reproduction process and new products obtained |
GB1827/53A GB726543A (en) | 1947-11-04 | 1953-01-21 | Improvements in processes of photographic reproduction |
GB1826/53A GB725667A (en) | 1947-11-04 | 1953-01-21 | Improvements in processes of photographic reproduction |
FR1092963D FR1092963A (en) | 1947-11-04 | 1953-01-21 | Process for preparing photolithographic printing plates and new products for the implementation of this process |
BE517066D BE517066A (en) | 1947-11-04 | 1953-01-21 | |
BE517064D BE517064A (en) | 1947-11-04 | 1953-02-21 |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US783914A US2596756A (en) | 1947-11-04 | 1947-11-04 | Photomechanical copy method |
US267482A US2763553A (en) | 1947-11-04 | 1952-01-21 | Lithographic offset printing process |
US267446A US2675313A (en) | 1947-11-04 | 1952-01-21 | Photographic reproduction process |
Publications (1)
Publication Number | Publication Date |
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US2763553A true US2763553A (en) | 1956-09-18 |
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ID=27401969
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
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US783914A Expired - Lifetime US2596756A (en) | 1947-11-04 | 1947-11-04 | Photomechanical copy method |
US783912A Expired - Lifetime US2592368A (en) | 1947-11-04 | 1947-11-04 | Gelatine silver halide emulsion layer containing a dihydroxy diphenyl tanning developing agent |
US267446A Expired - Lifetime US2675313A (en) | 1947-11-04 | 1952-01-21 | Photographic reproduction process |
US267482A Expired - Lifetime US2763553A (en) | 1947-11-04 | 1952-01-21 | Lithographic offset printing process |
Family Applications Before (3)
Application Number | Title | Priority Date | Filing Date |
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US783914A Expired - Lifetime US2596756A (en) | 1947-11-04 | 1947-11-04 | Photomechanical copy method |
US783912A Expired - Lifetime US2592368A (en) | 1947-11-04 | 1947-11-04 | Gelatine silver halide emulsion layer containing a dihydroxy diphenyl tanning developing agent |
US267446A Expired - Lifetime US2675313A (en) | 1947-11-04 | 1952-01-21 | Photographic reproduction process |
Country Status (5)
Country | Link |
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US (4) | US2596756A (en) |
BE (4) | BE485609A (en) |
DE (2) | DE874704C (en) |
FR (4) | FR980399A (en) |
GB (4) | GB655274A (en) |
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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 |
US3010389A (en) * | 1953-03-09 | 1961-11-28 | Buskes Willem Marie | Photographic transfer printing plates |
US3029727A (en) * | 1956-07-13 | 1962-04-17 | Polychrome Corp | Method and composition for fixing transfer image |
US3091528A (en) * | 1958-08-19 | 1963-05-28 | Chem Fab L Van Der Grinten N V | Process and light-sensitive sheets for the production of pigment images by transfer |
US3091529A (en) * | 1958-08-19 | 1963-05-28 | Chem Fab L Van Der Grinton N V | Process and light-sensitive screen-sheets for the production of pigment images by transfer |
US3106516A (en) * | 1960-07-28 | 1963-10-08 | Eastman Kodak Co | Photoconductography employing electrolytic images to harden or soften films |
US3106517A (en) * | 1960-07-28 | 1963-10-08 | Eastman Kodak Co | Photoconductography employing spongy images containing gelatin hardeners |
US3152969A (en) * | 1960-07-28 | 1964-10-13 | Eastman Kodak Co | Photoconductolithography employing hydrophobic images |
US3220837A (en) * | 1955-07-22 | 1965-11-30 | Polaroid Corp | Diffusion transfer to stratum of a silver image inked and used in printing |
US3278958A (en) * | 1955-03-31 | 1966-10-18 | Dick Co Ab | Method of imaging a photolithographic plate and elements for use in the preparation of same |
US3650742A (en) * | 1968-07-01 | 1972-03-21 | Eastman Kodak Co | Oleophilizing gelatinous images |
US4024085A (en) * | 1973-10-03 | 1977-05-17 | Fuji Photo Film Co., Ltd. | Gum removing solution for lithographic plate |
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US2710820A (en) * | 1952-09-18 | 1955-06-14 | Eastman Kodak Co | Formation of laminates using contact resins |
US2704712A (en) * | 1952-09-18 | 1955-03-22 | Eastman Kodak Co | Photographic copying process |
US2795504A (en) * | 1952-10-25 | 1957-06-11 | Dick Co Ab | Compositions for use in the manufacture of elements in reproduction |
US2747999A (en) * | 1953-03-16 | 1956-05-29 | Eastman Kodak Co | Photographic reproduction process |
DE954391C (en) * | 1953-06-05 | 1956-12-13 | Agfa Ag Fuer Photofabrikation | Halogen silver layers containing developer substances |
US2969015A (en) * | 1953-07-14 | 1961-01-24 | Dick Co Ab | Method of producing a spirit master from a positive and a duplicating process with same |
US2914404A (en) * | 1953-07-31 | 1959-11-24 | Blaupunkt Werke Gmbh | Method of producing two-dimensional circuits or circuit elements on supporting bases |
US2756143A (en) * | 1953-12-24 | 1956-07-24 | Eastman Kodak Co | Photographic reproduction process |
US2903964A (en) * | 1955-01-24 | 1959-09-15 | Eastman Kodak Co | Photographic spirit duplicating process |
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US2942975A (en) * | 1955-05-05 | 1960-06-28 | Keuffel & Esser Co | Photosensitive material |
US2873671A (en) * | 1955-05-11 | 1959-02-17 | Dick Co Ab | Copy process and materials for use in same |
US2834676A (en) * | 1955-07-19 | 1958-05-13 | Sperry Rand Corp | Photographic diffusion transfer process for producing multiple direct positive copies |
US2865745A (en) * | 1955-08-25 | 1958-12-23 | Eastman Kodak Co | Photographic reproduction process |
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US2856283A (en) * | 1956-05-07 | 1958-10-14 | Eastman Kodak Co | Photographic emulsion |
DE1200134B (en) * | 1957-05-09 | 1965-09-02 | Wilhelm Ritzerfeld | Printing form foil with a light-sensitive direct positive halogen silver layer and a translucent carrier |
BE636778A (en) * | 1959-04-10 | |||
BE590925A (en) * | 1959-05-20 | |||
US3060022A (en) * | 1959-07-13 | 1962-10-23 | Gen Aniline & Film Corp | Image transfer process |
US3146104A (en) * | 1959-12-21 | 1964-08-25 | Eastman Kodak Co | Silver halide sensitized lithographic printing plate |
US3295969A (en) * | 1961-04-12 | 1967-01-03 | Eastman Kodak Co | Photographic spirit duplicating process |
FR1333745A (en) * | 1962-03-14 | 1963-08-02 | Kodak Pathe | New photothermographic product and method of photographic reproduction using such product |
BE636329A (en) * | 1962-08-20 | |||
US3189448A (en) * | 1962-08-22 | 1965-06-15 | Eastman Kodak Co | Developing compositions used in photographic transfer processes |
US3189449A (en) * | 1962-10-01 | 1965-06-15 | Eastman Kodak Co | Colloid stratum transfer process |
US3240600A (en) * | 1963-01-16 | 1966-03-15 | Eastman Kodak Co | Colloid transfer process |
GB1053631A (en) * | 1963-01-16 | |||
DE1256541B (en) * | 1963-01-23 | 1967-12-14 | Eastman Kodak Co | Copier with a developing device for matrices with a grip edge |
US3345170A (en) * | 1964-06-05 | 1967-10-03 | Eastman Kodak Co | Light sensitive photographic elements containing developing agent precursors |
US3326687A (en) * | 1964-11-10 | 1967-06-20 | Eastman Kodak Co | Photographic colloid transfer system |
US3751161A (en) * | 1965-10-01 | 1973-08-07 | Itek Corp | Photographic image transfer apparatus |
DE2832530C2 (en) * | 1978-07-25 | 1984-08-02 | Du Pont de Nemours (Deutschland) GmbH, 4000 Düsseldorf | Photosensitive material for tanning development |
JPS6015262B2 (en) * | 1979-02-26 | 1985-04-18 | 富士写真フイルム株式会社 | Silver halide photographic material |
JPS5625729A (en) * | 1979-08-07 | 1981-03-12 | Fuji Photo Film Co Ltd | Silver halide photographic material |
JPS59188641A (en) | 1983-04-11 | 1984-10-26 | Fuji Photo Film Co Ltd | Silver halide photographic emulsion |
US5037734A (en) * | 1989-12-28 | 1991-08-06 | Eastman Kodak Company | Stabilized photographic element containing infrared sensitizing dye |
JP2739261B2 (en) * | 1991-05-07 | 1998-04-15 | 富士写真フイルム株式会社 | Image forming method |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3010389A (en) * | 1953-03-09 | 1961-11-28 | Buskes Willem Marie | Photographic transfer printing plates |
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US4024085A (en) * | 1973-10-03 | 1977-05-17 | Fuji Photo Film Co., Ltd. | Gum removing solution for lithographic plate |
Also Published As
Publication number | Publication date |
---|---|
FR980399A (en) | 1951-05-11 |
GB726543A (en) | 1955-03-23 |
BE485611A (en) | 1948-11-13 |
BE517066A (en) | 1954-11-26 |
FR1092963A (en) | 1955-04-28 |
FR980401A (en) | 1951-05-11 |
US2592368A (en) | 1952-04-08 |
US2675313A (en) | 1954-04-13 |
GB655274A (en) | 1951-07-18 |
GB655273A (en) | 1951-07-18 |
GB725667A (en) | 1955-03-09 |
BE517064A (en) | 1954-11-26 |
FR1089934A (en) | 1955-03-24 |
US2596756A (en) | 1952-05-13 |
BE485609A (en) | 1942-11-12 |
DE927307C (en) | 1955-05-23 |
DE874704C (en) | 1953-04-27 |
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