US2018657A - Photographic developer and method of preparing the same - Google Patents
Photographic developer and method of preparing the same Download PDFInfo
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- US2018657A US2018657A US658446A US65844633A US2018657A US 2018657 A US2018657 A US 2018657A US 658446 A US658446 A US 658446A US 65844633 A US65844633 A US 65844633A US 2018657 A US2018657 A US 2018657A
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- developer
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- gas
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
- B41C3/00—Reproduction or duplicating of printing formes
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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
- G03C5/305—Additives other than developers
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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
- G03F7/04—Chromates
Definitions
- This invention relates to the preparation of a printing surface by photographic methods, having for its object to provide such a method as will be low in operating costs and more efficient in use than those heretofore proposed.
- the present novelty lies not only in the production of the finished printing surface, but in the production of a means for photographically developing a sensitized emulsion, as well as in the treatment of the developed emulsion for certain purposes, and also includes the change from one type of emulsion to another during the development.
- Ihe primary object sought herein is to prepare the same photographic image, laid down in essentially bare and covered parts on the plate, but the covered parts are preferably charged or loaded with a material capable of forming gas when heated.v A coating capable of entrapping this gas when evolved, may be added to the image parts or to the whole surface of the plate (for example, a solution of rubber may be flowed over the entire surface, or such a solution or other sticky films as rosin in a.
- this gas producing material may be added to the original emulsion of either type (for example, camphor or menthol may be added to the silver type emulsion, or solids, strongly adsorbing gases, may be used as for instance carbon black or clays, as bentonite).
- camphor or menthol may be added to the silver type emulsion, or solids, strongly adsorbing gases, may be used as for instance carbon black or clays, as bentonite.
- the range of materials is w greater and, beside those given above for silver emulsions, there may be added certain salts, such as ammonium carbonate or borate, or organic materials such-as chloral hydrate.
- gas forming materials may be added during the developing of a silver image during the washout process (both types of emulsion) for baring the plate; before, during, or after the final hardening process; and/or placed in or upon the image after hardening. These may be combined 20 and the gas producing material added at more than one point.
- a support such as a plate or more especially paper having thereon an emulsion of the bichromate type with or without an intervening layer of stripping gelatine, the bichromate emulsion having a thickness of as much as seven ll thousandths of an inch.
- This emulsion is exposed photographically and when the stripping paper is used is then transferred face down to a plate and treated in the usual manner or as hereinafter disclosed to remove the paper back as well as to develop the emulsion to provide bare and covered portions of said plate. If no stripping paper is used then the emulsion is developed immediately after exposure. In this case.
- the exposed emulsion may be covered with sticky material as well known, which material may contain the gas producing substance, or said substance may be applied over or under said sticky material.
- sticky material as well known, which material may contain the gas producing substance, or said substance may be applied over or under said sticky material.
- These silver emulsions maybe of any suitable and well known formula including the well-known fast silver bromide emulsions of the process type, and containing sufllcient silver, of course, so that in the consequent development there will be formed metallic silver.
- the silver bromide emulsion lends itself admirably to my process.
- This sensitized medium is placed in a camera and subjected to light rays admitted through the camera lens to affect the sensitized emulsion in accordance with the object which is being pictured.
- This sensitized and exposed emulsion is then subjected photographically to development to bring out the latent reproduction or image of said object in black and white.
- This development of the silver image is properly done at lower temperatures than that of the ordinary and/or heretofore known practice, a practical range being 50-58 F. with considerable lower temperatures giving very good results.
- the light exposed portions of the emulsion are tanned or rendered insoluble in water, and the resultant developed image strengthened by the partial hardening of the contained gelatine as a 'result of the tanning.
- the exposed and developedimage now becomes, for all intents and purposes, one of a bichromated type ing of the gelatine and penetration of the development.
- a novel medium for reducing the silver of the emulsion to metallic silver which is itself oxidized by the development of the silver salt of the exposed image into a tanning compound, which latter is taken up by the gelatine of the emulsion at the reduced areas only thereof.
- a restrainer capable of stabilizing the reducer against air oxidation, and an accelerator to restore the normal rate of development without appreciably changing the tendency of the reducer to become air oxidized.
- the sodium carbonate is the base having in combination therewith the sodium hydroxide to 15 give penetration in the development, and also in combination with pyrocatechinas the reducing agent.
- the borax and the potassium bromide form the restrainer, the borax serving to stabilize the pyrocatechin, and the acetone is used as the 20 accelerator, it additionally serving to increase penetration.
- This acetone also furnishes gas at a later stage of the process since a small quantity thereof is taken up by the gelatine.
- a small quantity of urea say up to 3 to 5% of the entire 5 developer volume, may advantageously be used in addition to the foregoing. ingredients to assist the penetration of the developer.
- the borax prevents air oxidation of the pyrocatechin, and lowers the reduction potential or the speed of the development of the silver image, and the acetone raises the reduction potential for silver with only a slight change on the oxidizing power of the air, which however,
- the developed image may be photographically fixed or not as desired to suit the needs of practice, but I have found it unnecessary to fix it.
- the development is stopped by immersion for approxinately one minute in a 3% solution of boric acid, then immediately submitted for a short time to an alcohol bath for partial drying.
- the developed and partially dried print is then transferred in a well known manner face down (upon the surface of a support which may be the surface of a metallic plate or the like, and then the paper backing as well as'the stripping gelatine and the whites of the image are washed on leaving the developed and tanned image upon said support.
- the washing can be done with various chemicals including water, but forextremely satisfactory results an acidified salt solution, such as calcium chloride, has been used. This same washing can be applied to the bichromated type of emulsion as well as to that hereinbefore mentioned.
- the chloride is in a solution of 4 substantially 5% concentration, and preferably containing 4% of 1% of concentrated hydrochloric acid with respecttothe volume of the washing solution.
- a peculiarity-of this particular washing solution is that if the chloride is used unacidified, and if a straight hydrochloric acid solution isused, the washing is so materially delayed as to be sub stantially ineffective; but by acidifying the chloride as above stated, the washing is quickly and efiiciently accomplished.
- This material may be the hardening solution itself, or it may be added is to the washed image before or after: the same is hardened by the hardener.
- gas liberating materials may be found those broughtabout icy-(1) reaction, (2) adsorbed gas with slight decomposition, (3) easily go decomposable inorganic compounds (4) volatile or easily decomposable organic compounds.
- chromic acid 'withoxalic acid as well as chromic acid with hydrogen peroxide, both liberating as oxygen, and the former additionally giving oif Among the materials which can be used, covering .the second group of adsorbed gas with slight decompositio there may be listed charso coal, carbon black, fullers earth, talc, and clays.
- powdered oxides such as litharge, iron oxide, lead dioxide; also powdered metals such as aluminum, and bronze powder; powdered glass such as obtained from a Cottrell precipitator in the stack leading from a furnace burning powdered coal.
- salts serve admirably for this gas liberating material including Prussian blue; copper, nickel, cadmium, manganese, and calcium oxslates, carbonates, 40 and cyanides; iron carbonate, bismuth sub-carbonate. and bismuth sub-nitrater Paris green; baking powder; ammonium mercurous chloride; mercury oxides; calcium-peroxide; silver-peroxide.
- the easily decomposable inorganic compounds capable of liberating gas will be found sodium perborate, ammonium carbonates, sodium hypochlorite, ammonium borate, ammonium chromates, and .the bicarbonates of alkali metals.
- the materials which are volatile or easily decomposable organic compounds and capable of liberating gas are ammonium oxalate, oxalic acid, naphthalene, camphor, acetone,- menthol, chloral hydrate,.urlc acid, milk sugar, pinene (alpha), Wintergreen (oil), aniline, aloin, formaldehyde, hydrazine” salts such as hydrazinedicarboxylic acid, and.
- organic acids especially the members of the malonic acid series.
- water as such, or water 00 of crystallization as in gypsum or calcium sulphate will also-produce evolution of gas upon heat.
- they may be added to the hardened image by incorporatimin a sticky body I which may be rolled on top, or they may be sprinkled over and caused to adhere to the sticky body such as ink which is rolled over the top.
- finely powdered materials which contain adsorbed gasfimd when used as 10 gas liberating senta' may be applied over, under, or in the sticky' such as ordinary inks as prlntinginksor .-rollins -up inks; rosin in a solvent;-varnishes;'oils vegetable or animal,
- the printing surface is formed preferably by casting type metal or the like against the image and its support.
- material other than metal such as matrix material, pulp of various forms, etc. may be pressed against the image and its support to receive an impression corresponding to the image, although in the use of the last mentioned materials, no additional relief will result in the ultimate cast.
- the metal being hotwill affect the gas liberating chemical contained in the image, thereby liberating the gas which is'then entrapped by the medium or vehicle employed therefor, and the pressure of this gas so liberated will force the metal away from the normal plane of the image so as to add increased relief to the ultimate cast.
- the cast can be made in several ways such for example as flowing the molten' metal onto the image and its support, or utilizing said support as a wall of a mold, and additionally the metal can be given still further relief by withdrawal of either the supporting plate from the main body portion of the metal, or a withdrawal by vacuum process of a portion of the applied metal while still semi-molten from the supporting plate. It is apparent that'the metal can be applied at various pressures other than atmospheric, especially above. In certain instances where desired the metal plate may be chilled at substantially the time of contact of the'molten metal therewith, so as to set or instantaneously solidify said casting metal at the printing surface portion thereof. When the cast is removed, it will. be ready to be inked for printing purposes.
- a photographic developer capable of developing a silver image at temperatures as low as 30 11, wherein the cut-out is sharp, the swelling of the contained gelatine is penetration is fast,'said developer containing borax and acetone serving to stabilize the developer against air oxidation while maintaining a strong chemic activity against the metal oi.' the image.
- Y 15 2.
- a photographic developer the same comprising substantially 1115 grams NazCOa (11% solution), 10 grams NaOH 96% purity, 6 grams KBr, 16 grams borax, 7 grams acetone, 2 grams KaSzOr, and 5 grams pyrocatechin. 20
- a photographic developer capable of reuse comprising a batch developer for a latent silver image of the bromide type, having added thereto borax and acetone to stabilize the developer against air oxidation while maintaining a strong chemical activity against the sliver of the image.
- a photographic developer comprising sub-- stantially 122 grams NarCOs 10 grams NaOH (96% purity), 6 grams KBr, 16 grams borax, grams acetone, 2 grams KzSzOv, 5 grams pyrocatechin, and water suflicient to make one liter.
- a photographic developer capable of working at a temperature as low as 30 F. comprising substantially 122 grams NazCO: 10 grams NaOH (96% purity), 6 grams KBr, 16 grams borax, 7 grams acetone, 5 gramspyrocatechin, and water suflicient to make 2 liters.
- a photographic developer comprising substantially 1000 grams water, 100-125 grams NflzCOs, 1045 grams NaOH (96% purity), 5-7 grams KBr, 15-17 grams borax, 6-8 grams acetone, 1-3 grams K2820! and 4'-6 grams pyrocatechin.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Printing Plates And Materials Therefor (AREA)
- Manufacture Or Reproduction Of Printing Formes (AREA)
- Printing Methods (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Description
latentegl Oct. 2 9, i935 PHOTOGRAPHIC DEVELOPER AND METHOD a or PREPARING T E SAME Charles W. Bennett, Douglaston, N. Y., asaignor,
direct and mesne assignments, to Photo- Cast, Inc., Rochester, N. Y., a corporation of Q New York No Drawing. ApplicationFebrnary 24, 1933.
Serial No. 658,448
\ 9Claims. (on. -88) This invention relates to the preparation of a printing surface by photographic methods, having for its object to provide such a method as will be low in operating costs and more efficient in use than those heretofore proposed.
With these and other objects in view the invention resides in the novel steps and combina tions of steps constituting the method as will be disclosed more fully hereinafter and particularly pointed out in-the claims.
In order'that this invention may be better understood, it is said that there is much need at present for a simplified and an inexpensive method of producing a printing surface, particularly in the reproduction of news and/ or copy make-up, to the end that if several steps of the processes now in use can be eliminated, without sacrifice of the resultant printing surface, then much has been attained. This invention therefore is particularly directed to a simplification of preparation of such a printing surface, as well as the novel progressive and intermediate steps which naturally flow from the entire process. In other words, the present novelty lies not only in the production of the finished printing surface, but in the production of a means for photographically developing a sensitized emulsion, as well as in the treatment of the developed emulsion for certain purposes, and also includes the change from one type of emulsion to another during the development.
This invention constitutes in part a continuation of that disclosed in my copending application for U. S. Letters Patent filed June 9, 1930 under the Serial No. 460,102 and entitled Method of printing in that this application has for its purpose, the disclosure of a method of preparing a photographic image delineated on a plate and represented by bare and covered portions. While the copending application set forth the production of additional relief in the image on the plate, in this application the additional relief in the image itself is not the primary object, although such may be a secondary occurrence.
Ihe primary object sought herein, is to prepare the same photographic image, laid down in essentially bare and covered parts on the plate, but the covered parts are preferably charged or loaded with a material capable of forming gas when heated.v A coating capable of entrapping this gas when evolved, may be added to the image parts or to the whole surface of the plate (for example, a solution of rubber may be flowed over the entire surface, or such a solution or other sticky films as rosin in a. solvent may be applied selectively, with a roller as in rolling up with ink, to the covered {portion rep-" resenting the image) a I v Furthermore this gas producing material may be added to the original emulsion of either type (for example, camphor or menthol may be added to the silver type emulsion, or solids, strongly adsorbing gases, may be used as for instance carbon black or clays, as bentonite). In the dichromate emulsion the range of materials is w greater and, beside those given above for silver emulsions, there may be added certain salts, such as ammonium carbonate or borate, or organic materials such-as chloral hydrate.
These gas forming materials may be added during the developing of a silver image during the washout process (both types of emulsion) for baring the plate; before, during, or after the final hardening process; and/or placed in or upon the image after hardening. These may be combined 20 and the gas producing material added at more than one point.
The method of evolving this gas to produce a desired result is disclosed in another application for patent. Suffice it to say, by way of making 5 the intent more clear, this process cools-the plate while the front of the image is heated. Gas is evolved at the heated portions where the cooling is retarded by the image, resulting in increased relief of the casted metal, at such image parts.
It is apparent that such a lag in cooling at the image parts, allows another method of applying the gas forming material namely, to flow over the total surface a gas forming material, or an emulsion or solution of the same (as for instance ammonium carbonate or borate combinedwith rubber as latex). This surface is then prepared for casting for instance by drying, and casting the hot metal against the above film. Strong cooling 40 at the substantially bare parts prevents a rise in temperature necessary to evolve gas while, at the image parts, the cooling lags and gas is evolved, producing relief suflicient for many cases. This differential liberation of gas is not so generally an applicable as the liberation of gas from gas producing material selectively placed in or upon the image parts either before exposure, or during the process.
According to this process, there is contemplated lo the provision of a support such as a plate or more especially paper having thereon an emulsion of the bichromate type with or without an intervening layer of stripping gelatine, the bichromate emulsion having a thickness of as much as seven ll thousandths of an inch. This emulsion is exposed photographically and when the stripping paper is used is then transferred face down to a plate and treated in the usual manner or as hereinafter disclosed to remove the paper back as well as to develop the emulsion to provide bare and covered portions of said plate. If no stripping paper is used then the emulsion is developed immediately after exposure. In this case. and prior to the development, the exposed emulsion may be covered with sticky material as well known, which material may contain the gas producing substance, or said substance may be applied over or under said sticky material. Alternately there may be prepared a silver emulsion over gelatine on a paper support and wherein the thickness of the coating is quite appreciable, such for example as up to five thousandths of an inch for the silver emulsion, the gelatine underlying said emulsion being of any desired thickness and for use in stripping alone. These silver emulsions maybe of any suitable and well known formula including the well-known fast silver bromide emulsions of the process type, and containing sufllcient silver, of course, so that in the consequent development there will be formed metallic silver. The silver bromide emulsion lends itself admirably to my process.
This sensitized medium is placed in a camera and subjected to light rays admitted through the camera lens to affect the sensitized emulsion in accordance with the object which is being pictured. This sensitized and exposed emulsion is then subjected photographically to development to bring out the latent reproduction or image of said object in black and white. This development of the silver image is properly done at lower temperatures than that of the ordinary and/or heretofore known practice, a practical range being 50-58 F. with considerable lower temperatures giving very good results. During this development the light exposed portions of the emulsion are tanned or rendered insoluble in water, and the resultant developed image strengthened by the partial hardening of the contained gelatine as a 'result of the tanning. At this point the exposed and developedimage now becomes, for all intents and purposes, one of a bichromated type ing of the gelatine and penetration of the development. There is also contemplated in this developer a novel medium for reducing the silver of the emulsion to metallic silver which is itself oxidized by the development of the silver salt of the exposed image into a tanning compound, which latter is taken up by the gelatine of the emulsion at the reduced areas only thereof. Also there is preferably provided a restrainer capable of stabilizing the reducer against air oxidation, and an accelerator to restore the normal rate of development without appreciably changing the tendency of the reducer to become air oxidized.
- Various chemical elements and compounds may be found suitable for accomplishing this development, as just stated, but from actual practice it has been found that one which is very eflicient and cheap is wherein the sodium carbonate is a water solution and the sodium hydroxide is of 96% purity.
The sodium carbonate is the base having in combination therewith the sodium hydroxide to 15 give penetration in the development, and also in combination with pyrocatechinas the reducing agent. The borax and the potassium bromide form the restrainer, the borax serving to stabilize the pyrocatechin, and the acetone is used as the 20 accelerator, it additionally serving to increase penetration. This acetone also furnishes gas at a later stage of the process since a small quantity thereof is taken up by the gelatine. A small quantity of urea, say up to 3 to 5% of the entire 5 developer volume, may advantageously be used in addition to the foregoing. ingredients to assist the penetration of the developer.
However, though borax as a restrainer and preservative has been previously used as well 30 as acetone as an accelerator in about a 3% solution, it is particularly pointed out that the action obtained according to this invention is different from the ordinary restraining and accelerating action of these agencies. That is to say if the acetone is left out, the development is just as rapid for one or two prints but after the second print the developer will not function. 0n the other hand, by the use of acetone (in quantity less than 1% by volume of the total developer) in combination, a developer is obtained which can be reused satisfactorily for making a large number of prints. It appears therefore that this result is not contemplated in the mere acceleration according to previous disclosures. The borax prevents air oxidation of the pyrocatechin, and lowers the reduction potential or the speed of the development of the silver image, and the acetone raises the reduction potential for silver with only a slight change on the oxidizing power of the air, which however,
by this invention, has been discovered to yield an advantageous result. This advantage is unexpected in that it was not foreseen that there could be obtained a stability to air while maintaining strong chemical activity as against silver, and hence a new combination is produced in the elements of this developer.
The foregoing may be stated differently as follows. Heretofore, sodium hydroxide develops were known as batch developers, that is to say one print could be developed therewith after which the developer was thrown away. This is contradistinguishable to carbonate or sulphite developers which will last for some time. By this invention there is produced a developer (which has a concentration of alkali comparable with present day batch developers) which has the beneficial advantages of a carbonate or sulphite developer as used today. ,Before the above advantageous combination of borax and acetone was discovered, the development of prints was in batches, but now the present developer can be reused while producing good prints. In other words, by combining the borax and acetone an Tl This developer can be used at various temperiatures, a surprising result being that it has beenbeen found that a developer containing a lower nncentration of the above ingredients has very successfully worked at a temperature as low as 30 F. and, of course, willlikewise work at temperatures thereabove and more in the range of the heretofore known developers. The pyrocatechin in reducing the silver salt of the emulsion of the latent image to metallic silver, concurrently forms a tanning compound acting upon the gelatine of the emulsion at the reduced areas only, to harden the gelatine at said areas, and the hydroxide is found to facilitate the penetration as well as to intensify the tanning action. The developed image may be photographically fixed or not as desired to suit the needs of practice, but I have found it unnecessary to fix it. The development is stopped by immersion for approxinately one minute in a 3% solution of boric acid, then immediately submitted for a short time to an alcohol bath for partial drying.
- The developed and partially dried print is then transferred in a well known manner face down (upon the surface of a support which may be the surface of a metallic plate or the like, and then the paper backing as well as'the stripping gelatine and the whites of the image are washed on leaving the developed and tanned image upon said support. The washing can be done with various chemicals including water, but forextremely satisfactory results an acidified salt solution, such as calcium chloride, has been used. This same washing can be applied to the bichromated type of emulsion as well as to that hereinbefore mentioned.
The chloride is in a solution of 4 substantially 5% concentration, and preferably containing 4% of 1% of concentrated hydrochloric acid with respecttothe volume of the washing solution. a peculiarity-of this particular washing solution is that if the chloride is used unacidified, and if a straight hydrochloric acid solution isused, the washing is so materially delayed as to be sub stantially ineffective; but by acidifying the chloride as above stated, the washing is quickly and efiiciently accomplished.
As a result of the development, it is highly desirable to keepall portions of the tanned gelatine fixed or immobile with respect to the support to which it is transferred, for should any disturbance of the gelatine occur, there maybe a serious defect in the resultant formation of the image, and the printing surface-which may be produced therefrom. By the use of this acidified solution of calcium chloride, this result is insured namely, the fixation of the gelatine with respect to the support, in that there is no tendency to loosen the image from the support I v The completely developed and washed image, transferredtothesupporhiathenreadyfora further treatment tending to render said image hard and capable of withstanding considerable handling as well as the possible formation of the printing surface in manners including casting of metal against this image. It has been found practical to include in the hardening agent, ap plied at this stage of the process,,a chemical or substance which will be somewhat absorbed by thergelatine so that there will be a quantity thereof in the resultant washed image to produce a' gas in the printing surface formation.
There is desired a wide latitude in the selecence has shown that excellent results can be obtained with many. This material may be the hardening solution itself, or it may be added is to the washed image before or after: the same is hardened by the hardener.
Among the gas liberating materials may be found those broughtabout icy-(1) reaction, (2) adsorbed gas with slight decomposition, (3) easily go decomposable inorganic compounds (4) volatile or easily decomposable organic compounds. Under the heading of reactions there may be cited chromic acid 'withoxalic acid as well as chromic acid with hydrogen peroxide, both liberating as oxygen, and the former additionally giving oif Among the materials which can be used, covering .the second group of adsorbed gas with slight decompositio there may be listed charso coal, carbon black, fullers earth, talc, and clays. In addition there are powdered oxides such as litharge, iron oxide, lead dioxide; also powdered metals such as aluminum, and bronze powder; powdered glass such as obtained from a Cottrell precipitator in the stack leading from a furnace burning powdered coal. Also many salts serve admirably for this gas liberating material including Prussian blue; copper, nickel, cadmium, manganese, and calcium oxslates, carbonates, 40 and cyanides; iron carbonate, bismuth sub-carbonate. and bismuth sub-nitrater Paris green; baking powder; ammonium mercurous chloride; mercury oxides; calcium-peroxide; silver-peroxide.
Among the easily decomposable inorganic compounds capable of liberating gas will be found sodium perborate, ammonium carbonates, sodium hypochlorite, ammonium borate, ammonium chromates, and .the bicarbonates of alkali metals. On the other hand, the materials which are volatile or easily decomposable organic compounds and capable of liberating gas, are ammonium oxalate, oxalic acid, naphthalene, camphor, acetone,- menthol, chloral hydrate,.urlc acid, milk sugar, pinene (alpha), Wintergreen (oil), aniline, aloin, formaldehyde, hydrazine" salts such as hydrazinedicarboxylic acid, and. organic acids especially the members of the malonic acid series. In addition to the foregoing, water as such, or water 00 of crystallization as in gypsum or calcium sulphate, will also-produce evolution of gas upon heat. In any of the foregoing-materials itwill be understood that they may be added to the hardened image by incorporatimin a sticky body I which may be rolled on top, or they may be sprinkled over and caused to adhere to the sticky body such as ink which is rolled over the top.
In addition, the finely powdered materials which contain adsorbed gasfimd when used as 10 gas liberating senta'may be applied over, under, or in the sticky' such as ordinary inks as prlntinginksor .-rollins -up inks; rosin in a solvent;-varnishes;'oils vegetable or animal,
straight, v by heat, and in combination; II.
tion of the, gas producing materials since experithe most efllcient and may be applied by flowing,
or spraying. When using such a rubber solution' it will, of course, cover the otherwise bare portions of the metal plate constituting the support for the image as well as the image itself, but this is not detrimental. On the other hand,
it is advantageous since it produces a cementitious bond between the metal which may be cast against the image and the support, and the surface of said support, so that additional relief beyond ordinary may be obtained in the resultant cast. 1
'The printing surface is formed preferably by casting type metal or the like against the image and its support. On the other hand, material other than metal such as matrix material, pulp of various forms, etc. may be pressed against the image and its support to receive an impression corresponding to the image, although in the use of the last mentioned materials, no additional relief will result in the ultimate cast. The metal, however, being hotwill affect the gas liberating chemical contained in the image, thereby liberating the gas which is'then entrapped by the medium or vehicle employed therefor, and the pressure of this gas so liberated will force the metal away from the normal plane of the image so as to add increased relief to the ultimate cast.
The cast can be made in several ways such for example as flowing the molten' metal onto the image and its support, or utilizing said support as a wall of a mold, and additionally the metal can be given still further relief by withdrawal of either the supporting plate from the main body portion of the metal, or a withdrawal by vacuum process of a portion of the applied metal while still semi-molten from the supporting plate. It is apparent that'the metal can be applied at various pressures other than atmospheric, especially above. In certain instances where desired the metal plate may be chilled at substantially the time of contact of the'molten metal therewith, so as to set or instantaneously solidify said casting metal at the printing surface portion thereof. When the cast is removed, it will. be ready to be inked for printing purposes.
It is obvious that those skilled'in the art may vary the steps and combinations of steps conaoraesv stituting the method as well as the component 1 parts of the developer, without departing from the spirit of the invention, and therefore it is not desired tobe limited to the foregoing except as may be required by-the claims. 5
What is claimed is:
1. .A photographic developer capable of developing a silver image at temperatures as low as 30 11, wherein the cut-out is sharp, the swelling of the contained gelatine is penetration is fast,'said developer containing borax and acetone serving to stabilize the developer against air oxidation while maintaining a strong chemic activity against the metal oi.' the image. Y 15 2. A photographic developer the same comprising substantially 1115 grams NazCOa (11% solution), 10 grams NaOH 96% purity, 6 grams KBr, 16 grams borax, 7 grams acetone, 2 grams KaSzOr, and 5 grams pyrocatechin. 20
3. A photographic developer capable of reuse comprising a batch developer for a latent silver image of the bromide type, having added thereto borax and acetone to stabilize the developer against air oxidation while maintaining a strong chemical activity against the sliver of the image.
4. The method of stabilizing a photographic batch developer for a latent silver image of the bromide type, which consists in adding borax and acetone thereto.
5. The method of stabilizing a photographic batch developer for a latent silver image of the bromide type and containing 10-15 grams of sodium hydroxide per liter, which consists in adding borax and acetone thereto. Y 6. The method of stabilizing a photographic batch developer for a latent silver image of the bromide type and containing 1045 grams of sodium hydroxide per liter, which consists in adding approximately 15 grams of borax and 6 grams 0 of acetone per liter thereto.
'7. A photographic developer comprising sub-- stantially 122 grams NarCOs 10 grams NaOH (96% purity), 6 grams KBr, 16 grams borax, grams acetone, 2 grams KzSzOv, 5 grams pyrocatechin, and water suflicient to make one liter.
8. A photographic developer capable of working at a temperature as low as 30 F. comprising substantially 122 grams NazCO: 10 grams NaOH (96% purity), 6 grams KBr, 16 grams borax, 7 grams acetone, 5 gramspyrocatechin, and water suflicient to make 2 liters. p I
9. A photographic developer comprising substantially 1000 grams water, 100-125 grams NflzCOs, 1045 grams NaOH (96% purity), 5-7 grams KBr, 15-17 grams borax, 6-8 grams acetone, 1-3 grams K2820! and 4'-6 grams pyrocatechin.
CHARLES W. BENNE'I'I. o0
inappreciable, and the 10
Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US460102A US1952787A (en) | 1930-06-09 | 1930-06-09 | Method of printing |
US528435A US1919194A (en) | 1930-06-09 | 1931-04-07 | Method of making a printing surface |
US658446A US2018657A (en) | 1930-06-09 | 1933-02-24 | Photographic developer and method of preparing the same |
GB12082/33A GB407834A (en) | 1930-06-09 | 1933-04-25 | Method of making a printing surface |
NL65122A NL35923C (en) | 1930-06-09 | 1933-04-28 | |
FR755134D FR755134A (en) | 1930-06-09 | 1933-05-04 | Process for producing a printing surface |
BE396084D BE396084A (en) | 1930-06-09 | 1933-05-04 | |
DEB160836D DE645361C (en) | 1930-06-09 | 1933-05-11 | Process for the production of high-pressure forms by molding gelatin reliefs, which evolve from heat, using liquid metal |
US681228A US1990925A (en) | 1930-06-09 | 1933-07-19 | Method of preparing a plate for printing purposes |
BE411607D BE411607A (en) | 1930-06-09 | 1935-10-05 | |
FR795992D FR795992A (en) | 1930-06-09 | 1935-10-05 | Photographic developer and its stabilization process |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US460102A US1952787A (en) | 1930-06-09 | 1930-06-09 | Method of printing |
US528435A US1919194A (en) | 1930-06-09 | 1931-04-07 | Method of making a printing surface |
US658446A US2018657A (en) | 1930-06-09 | 1933-02-24 | Photographic developer and method of preparing the same |
DEB160836D DE645361C (en) | 1930-06-09 | 1933-05-11 | Process for the production of high-pressure forms by molding gelatin reliefs, which evolve from heat, using liquid metal |
US681228A US1990925A (en) | 1930-06-09 | 1933-07-19 | Method of preparing a plate for printing purposes |
Publications (1)
Publication Number | Publication Date |
---|---|
US2018657A true US2018657A (en) | 1935-10-29 |
Family
ID=40822991
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US460102A Expired - Lifetime US1952787A (en) | 1930-06-09 | 1930-06-09 | Method of printing |
US528435A Expired - Lifetime US1919194A (en) | 1930-06-09 | 1931-04-07 | Method of making a printing surface |
US658446A Expired - Lifetime US2018657A (en) | 1930-06-09 | 1933-02-24 | Photographic developer and method of preparing the same |
US681228A Expired - Lifetime US1990925A (en) | 1930-06-09 | 1933-07-19 | Method of preparing a plate for printing purposes |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US460102A Expired - Lifetime US1952787A (en) | 1930-06-09 | 1930-06-09 | Method of printing |
US528435A Expired - Lifetime US1919194A (en) | 1930-06-09 | 1931-04-07 | Method of making a printing surface |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US681228A Expired - Lifetime US1990925A (en) | 1930-06-09 | 1933-07-19 | Method of preparing a plate for printing purposes |
Country Status (6)
Country | Link |
---|---|
US (4) | US1952787A (en) |
BE (2) | BE396084A (en) |
DE (1) | DE645361C (en) |
FR (2) | FR755134A (en) |
GB (1) | GB407834A (en) |
NL (1) | NL35923C (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2606117A (en) * | 1947-06-05 | 1952-08-05 | Gen Aniline & Film Corp | Diazotype photoprinting materials |
US2656272A (en) * | 1950-11-30 | 1953-10-20 | Gen Aniline & Film Corp | Stabilized azine photographic developers containing sodium metaborate as the sole alkali |
US2703756A (en) * | 1951-12-12 | 1955-03-08 | Gen Aniline & Film Corp | Vesicular prints and process of making same |
US2911299A (en) * | 1952-07-22 | 1959-11-03 | Kalvar Corp | System of photographic reproduction |
US3001873A (en) * | 1956-03-22 | 1961-09-26 | Ncr Co | Photo-printing process and material |
DE1117386B (en) * | 1958-06-28 | 1961-11-16 | Pharmacia Ab | Photographic developer |
US3129097A (en) * | 1959-07-01 | 1964-04-14 | Gevaert Photo Prod Nv | Manufacture of photographic gelatin relief images |
DE3337641A1 (en) * | 1982-10-25 | 1984-05-10 | Heribert 5163 Langerwehe Schain | Developer for imagewise development of document films |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB587023A (en) * | 1944-11-03 | 1947-04-10 | Arthur Stanley Briggs | The production of rubbers and plastics in sponge-like or cellular form |
US2532390A (en) * | 1945-05-28 | 1950-12-05 | Preparation of a printing surface | |
US2569936A (en) * | 1947-11-08 | 1951-10-02 | Hall Lab Inc | Phosphate product and method of making same |
US2610157A (en) * | 1948-09-24 | 1952-09-09 | Monsanto Chemicals | Porous composition utilizing n-carboxylic acid anhydrides of amino carboxylic acids |
US2634243A (en) * | 1949-12-22 | 1953-04-07 | Us Rubber Co | Production of gas-expanded organic plastics |
US2621161A (en) * | 1950-02-23 | 1952-12-09 | Us Rubber Co | Making gas-expanded organic plastics |
US2598078A (en) * | 1950-06-22 | 1952-05-27 | Us Rubber Co | Preparation of gas-expanded plastic materials |
US2709654A (en) * | 1950-09-29 | 1955-05-31 | Adalbert B Guth | Thermographic method of producing relief and intaglio impressions |
US2748022A (en) * | 1952-08-08 | 1956-05-29 | Eastman Kodak Co | Cellulose ester photographic emulsions |
US2875047A (en) * | 1955-01-19 | 1959-02-24 | Oster Gerald | Photopolymerization with the formation of coherent plastic masses |
GB814299A (en) * | 1955-11-09 | 1959-06-03 | Thos J Moran Sons Inc | Improvements in or relating to photographic reliefs |
US3108872A (en) * | 1961-09-27 | 1963-10-29 | Photo-thermolytical vesicular | |
GB1080364A (en) * | 1963-03-28 | 1967-08-23 | Nat Res Dev | Preparation of diffraction gratings |
US4128422A (en) * | 1976-11-08 | 1978-12-05 | Eastman Kodak Company | Cyclopropenone vesicular imaging composition, element and process |
US4379830A (en) * | 1981-10-06 | 1983-04-12 | Polychrome Corporation | Developer for positive photolithographic articles |
-
1930
- 1930-06-09 US US460102A patent/US1952787A/en not_active Expired - Lifetime
-
1931
- 1931-04-07 US US528435A patent/US1919194A/en not_active Expired - Lifetime
-
1933
- 1933-02-24 US US658446A patent/US2018657A/en not_active Expired - Lifetime
- 1933-04-25 GB GB12082/33A patent/GB407834A/en not_active Expired
- 1933-04-28 NL NL65122A patent/NL35923C/xx active
- 1933-05-04 BE BE396084D patent/BE396084A/xx unknown
- 1933-05-04 FR FR755134D patent/FR755134A/en not_active Expired
- 1933-05-11 DE DEB160836D patent/DE645361C/en not_active Expired
- 1933-07-19 US US681228A patent/US1990925A/en not_active Expired - Lifetime
-
1935
- 1935-10-05 FR FR795992D patent/FR795992A/en not_active Expired
- 1935-10-05 BE BE411607D patent/BE411607A/xx unknown
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2606117A (en) * | 1947-06-05 | 1952-08-05 | Gen Aniline & Film Corp | Diazotype photoprinting materials |
US2656272A (en) * | 1950-11-30 | 1953-10-20 | Gen Aniline & Film Corp | Stabilized azine photographic developers containing sodium metaborate as the sole alkali |
US2703756A (en) * | 1951-12-12 | 1955-03-08 | Gen Aniline & Film Corp | Vesicular prints and process of making same |
US2911299A (en) * | 1952-07-22 | 1959-11-03 | Kalvar Corp | System of photographic reproduction |
US3001873A (en) * | 1956-03-22 | 1961-09-26 | Ncr Co | Photo-printing process and material |
DE1117386B (en) * | 1958-06-28 | 1961-11-16 | Pharmacia Ab | Photographic developer |
US3129097A (en) * | 1959-07-01 | 1964-04-14 | Gevaert Photo Prod Nv | Manufacture of photographic gelatin relief images |
DE3337641A1 (en) * | 1982-10-25 | 1984-05-10 | Heribert 5163 Langerwehe Schain | Developer for imagewise development of document films |
Also Published As
Publication number | Publication date |
---|---|
US1919194A (en) | 1933-07-25 |
NL35923C (en) | 1935-07-15 |
DE645361C (en) | 1937-05-26 |
US1990925A (en) | 1935-02-12 |
US1952787A (en) | 1934-03-27 |
BE396084A (en) | 1933-06-30 |
FR795992A (en) | 1936-03-26 |
GB407834A (en) | 1934-03-29 |
BE411607A (en) | 1935-11-30 |
FR755134A (en) | 1933-11-17 |
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