US2183447A - Light-sensitive material and method of making the same - Google Patents

Light-sensitive material and method of making the same Download PDF

Info

Publication number
US2183447A
US2183447A US222536A US22253638A US2183447A US 2183447 A US2183447 A US 2183447A US 222536 A US222536 A US 222536A US 22253638 A US22253638 A US 22253638A US 2183447 A US2183447 A US 2183447A
Authority
US
United States
Prior art keywords
film
light
solution
image
support
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US222536A
Inventor
Dippel Cornelis Johannes
Alink Roelef Jan Hendrik
Kouning Klaas Jannes
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Koninklijke Philips NV
Original Assignee
Philips Gloeilampenfabrieken NV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Philips Gloeilampenfabrieken NV filed Critical Philips Gloeilampenfabrieken NV
Application granted granted Critical
Publication of US2183447A publication Critical patent/US2183447A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/52Compositions containing diazo compounds as photosensitive substances
    • G03C1/62Metal compounds reducible to metal

Definitions

  • Our invention relates to light-sensitive layers, to a method of making the same, and to a method of obtaining contrasts therewith.
  • this image can be given a high covering power and a high density by physical development" with a silver salt.
  • the object of the present invention is to materially reduce the gradation value of the images formed on such materiaL'and for this purpose we use as a support a transparent lyophile film and provide the same with a colloidally-dispersed material which during formation of the image does not, or substantially does not, dissolve in the solution used for the physical development and which causes local variations in the concentration of the photo-sensitive diazonium compound in the film.
  • a lyophile film supporting material having a a great afilnity with respect to polar solvents we preferably use regenerated cellulose, but other materials, for instance cellulose derivatives, such as acetyl cellulose and gelatine foils may also be used 50
  • cellulose derivatives such as acetyl cellulose and gelatine foils
  • the colloidally-dispersed material may be either introduced into the support during the manufacture thereof, or formed as a colloidal precipitate in thesupport by'means of a chemical reaction.
  • the gradation value of the image can be controlled within wide limits by varying the quantity of the colloidally-dispersed material contained within the transparent film, and can be made smaller by increasing the quantity of the oolloidally-dispersed material.
  • the selection of the colloidally-dispersed material used in any particular case depends upon practical considerations.
  • the materials introduced or to be introduced into the support must not react with each other in an undesirable manner, and it is, of course, preferable to use materials which do not cause excessive fogging.
  • Practical circumstances must also be considered for the applicationof the colloidally-dispersed material. For example, if it is desired to form the oolloidallydispersed material by means of aprecipitation reaction, care should be taken'that the concerntration of the solutions are so chosen that the precipitate arises in the film itself.
  • Example I a A transparent film consisting of regenerated cellulose of a thickness of about 40a is soaked for several minutes in a nitric solution of bismuth nitrate, which may be prepared in the following manner:
  • an aqueous solution which contains 5% bismuth nitrate and 4% nitric acid.
  • the film is then introduced into a solution containing two parts by volume of ethanol (CzHsOH) and one part by volume of water.
  • the film is allowed to remain for 5 to 10 minutes in this solution while agitating the liquid,' and as a result the bismuth nitrate is hydrolised.
  • the adhering excess liquid is removed, and. the film is dried in air.
  • the film thus prepared is then soaked for several minutes in a solution obtained by mixing:
  • Example II A film of regenerated cellulose, provided with a basic bismuth nitrate precipitate in the manner described in Example I, is sensitized by means of the following solution:
  • a metal image is then obtained 'on the film by physical development in the manner described in Example I.
  • Ea'arizple ZZZ A film is provided with basic bismuth nitrate in the manner described in Example I, and is sensitized by the application of the following solution:
  • Example IV A film of superficially saponified acetyl cellulose is provided with basic bismuth nitrate in the manner described in Example I and is then sensitized with the following solution:
  • the further treatment is the same; namely, rinsing for about 15 minutes in running water, bathing .for about 15 minutes in distilled Water, blotting between filter paper, and drying in. ail.
  • films containing bismuth which are often opalescent are substantially as transparent as films that have not been treated.
  • Example VI Two similar cellulose films were treated according to Example V treatment 0 and sensitized. Subsequently one of these films was bathed for about one minute in ethanol of 55% to which is added 0.1 part by volume of glycerol. After removing the adhering excess liquid, the film was dried in air. The films were then exposed in a similar manner. After physical development, it was found that the film subjected to the aftertreatment is softer than a film which was not treated; the gradation value being 2.0 and 3.4 respectively.
  • a light-sensitive material adapted to be physically-developed after exposure bythe application of a developing solution comprising a support of a transparent lyophile colloid of the type of regenerated cellulose and cellulose derivatives, a light-sensitive system within a portion of said support and comprising a diazonium com- I pound and a metal salt which is reducible to a metal in an aqueous solution, and means within said portion to produce. local variations in the concentration of the diazonium compound and to reduce the gradation value of the light-sensitive system, said means comprising a colloidallydispersed material which is substantially not dissolved by the developing solution during the formation of the image.
  • a light-sensitive material adapted to be physically-developed after exposure by the application of a developing solution comprising a support of transparent regenerated cellulose, a lightsensitive system within a portion of said support and comprising a diazonium compound and a metal salt which is reducible to a metal in an aqueous solution, and means within said portion to produce local variations in the concentration of the diazonium compound and to reduce the gradation value of the light-sensitive system, said means comprising a oolloidally-dispersed material which is substantially not dissolved by the developing solution during the formation of the image.
  • a light-sensitive material adapted to be physically-developed after exposure by the application of a developing solution
  • a developing solution comprising a support of a transparent cellulose derivative of the type of acetyl cellulose and gelatin material, a light-sensitive system within a portion of said support and comprising a diazonium compound and a metal salt which is reducible to a metal in an aqueous solution, and means within said portion to produce local variations in the concentration of the diazonium compound and to reduce.
  • the gradation value of the light-sensitive system said means comprising a colloidally-dispersed material'which is substantially not dissolved by the developing solution during the formation of the image.
  • a light-sensitive material adapted to be physically developed after exposure by the application of a developing solution comprising a support of a transparent lyophile colloid, a lightsensitive system within a portion of said support and comprising a diazonium compound and a metal salt which is reducible to a metal in an aqueous solution, and means within said portion to produce local variations in the concentration of the diazonium compound and to reduce the gradation value of the light-sensitive system, said means comprising colloidally-dispersed basic bismuth nitrate.
  • a method of photo-chemically pro d ucing contrasts comprising the steps of placing a diazonium compound within a portion of a support of a transparent lyophile colloid to.form a lightsensitive system, incorporating within the said portion of the support to produce local variations in the concentration of the diazonium compounds coiloidally-dispersed material which is substantially not dissolved in the developing solution, selectively exposing the so-treated support to light, and physically developing the exposed support by applying to said portion a developing solution containing a metal salt reducible to a metal in an aqueous solution.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)

Description

Patented Dec. 12, 1939 UNITED STATES. l
ATENT OFFICE GET-SENSITIVE MATERIAL MAKING THE S m us'rnon AME 6 Claims.
Our invention relates to light-sensitive layers, to a method of making the same, and to a method of obtaining contrasts therewith.
In the photo-chemical production of contrasts it is known to produce a metal image by means of a photo-sensitive diazonium compound and a metal salt which can be reduced tov form metal in an aqueous solution. For example, it has been proposed to produce in this way a silver image 0 by means of a silver salt, and in the U. 8. Patent 2,067,690 to Alink et al. excellent results are obtained by means of a diazonium compound and a mercurous salt. In the latter case a mercury image is obtained which gives excellent contrasts,
15 and this image can be given a high covering power and a high density by physical development" with a silver salt.
The term "physical development", as used herein and in the claims is to be understood to 0 mean a development in which, prior to the deso a high gamma, which is a disadvantage as regards general use of the method for photographic purposes.
The object of the present invention is to materially reduce the gradation value of the images formed on such materiaL'and for this purpose we use as a support a transparent lyophile film and provide the same with a colloidally-dispersed material which during formation of the image does not, or substantially does not, dissolve in the solution used for the physical development and which causes local variations in the concentration of the photo-sensitive diazonium compound in the film.
As a lyophile film supporting material having a a great afilnity with respect to polar solvents we preferably use regenerated cellulose, but other materials, for instance cellulose derivatives, such as acetyl cellulose and gelatine foils may also be used 50 We have found that when using a film such as described above, the gradation value obtained after development is considerably lower than it would have been without using the invention. This is probably due to the fact that a film according to the invention has the property that, with a homogeneous exposure followed by physical development, local variations of the quantity of the deposited metal forming the image are obtained.
1mm. Application August 1, 1m, Serial 222,536. In Germany August 9, 1937 The colloidally-dispersed material may be either introduced into the support during the manufacture thereof, or formed as a colloidal precipitate in thesupport by'means of a chemical reaction. The gradation value of the image can be controlled within wide limits by varying the quantity of the colloidally-dispersed material contained within the transparent film, and can be made smaller by increasing the quantity of the oolloidally-dispersed material.
In carrying out the invention, the selection of the colloidally-dispersed material used in any particular case depends upon practical considerations. For example, the materials introduced or to be introduced into the support must not react with each other in an undesirable manner, and it is, of course, preferable to use materials which do not cause excessive fogging. Practical circumstances must also be considered for the applicationof the colloidally-dispersed material. For example, if it is desired to form the oolloidallydispersed material by means of aprecipitation reaction, care should be taken'that the concerntration of the solutions are so chosen that the precipitate arises in the film itself. It may occur, for instance, that a material introduced has for the greater part already been expelled by dif-- fusion from the film before the concentration of a second material necessary for the precipitate in the film is sufilcient to produce the precipitate in the film. To avoid this the concentration of this second reagent solution should be made sufflciently strong. Furthermore, in some cases the precipitate might be soluble in an excess of the above-mentioned reagent solution. In such a case, the concentration of the reagent solution must be sufficiently weakto avoid the last-mentioned drawback. If, with a certain precipitation reaction, the relationship of the solubility conditions of the reacting materials are such that suitable concentrations cannot be found, this combination is in the nature of things unsuitable for the preparation of a film according to the invention. In such a case, however, it may be possible to provide the material to be colloidally dispersed, in some other manner in the him, for instance during the manufacture of the support material itself.
From the above it appears that materials which are suitable for carrying out the invention can be selected by one skilled in the art from the point of view of diazonium compound-adsorbing capacity whilst being in the colloidal dispersed state.
In order that the invention may be clearly an readily carried into effect, we shall describe the samein more detail with reference to several examples. 4
Example I a A transparent film consisting of regenerated cellulose of a thickness of about 40a is soaked for several minutes in a nitric solution of bismuth nitrate, which may be prepared in the following manner:
5 gms. of basic bismuth nitrate (BiONOaHzO) are mixed with 2.2 cos. of nitric acid (sp. gr. 1.4); a solid mass arising with the production of heat. Subsequently cos. of water and 2.5 cos. of nitric acid (sp. gr. 1.4) are added in which this solid material dissolves. Upon dilution with 3.2 ccs.
' of nitric acid (sp. gr. 1.4) and 103 cos. of water,
an aqueous solution is produced which contains 5% bismuth nitrate and 4% nitric acid.
The excess solution is then removed by pass- I ing the film between suitable rolls.
The film is then introduced into a solution containing two parts by volume of ethanol (CzHsOH) and one part by volume of water. The film is allowed to remain for 5 to 10 minutes in this solution while agitating the liquid,' and as a result the bismuth nitrate is hydrolised. The adhering excess liquid is removed, and. the film is dried in air.
The film thus prepared is then soaked for several minutes in a solution obtained by mixing:
Diazonium-2 hydroxy-l methyl-6 benzene sulphonic acid-4 gms 2.0 Mercurous nitrate (HgNOaHzO).. gms 2.5 Nitric acid (sp. gr. 1.4) cc 0.75 94% ethanol ccs 86 Water ccs 21 Glycerol ccs 10 quantity of the bismuth compound is added to the film. The color of the image also depends on the quantity of the bismuth compound used, and with a larger quantity the color of the image changes from black to a ratherbrown tone.
Example II A film of regenerated cellulose, provided with a basic bismuth nitrate precipitate in the manner described in Example I, is sensitized by means of the following solution:
Double salt of p-diethylamino-benz ene-diazonium chloride and zinc chloride-..gms.. 2.0 Silver nitrate em 4.1 Tartaric acid g 1.0 Water ccs 65 94% ethanol ccs..; 25 Glycerolccs 10 The adhering excess liquid is removed and the film dried in air.
A metal image is then obtained 'on the film by physical development in the manner described in Example I.
Ea'arizple ZZZ A film is provided with basic bismuth nitrate in the manner described in Example I, and is sensitized by the application of the following solution:
p-Diphenylamino-tlazonium sulphate-gms 5.0 Silver nitrate gms 5.0 Wateros" 175 The film is then treated in the manner described in Example I whereby a metal image is obtained by physical development.
Example IV A film of superficially saponified acetyl cellulose is provided with basic bismuth nitrate in the manner described in Example I and is then sensitized with the following solution:
Diazonium-2 methyl-8 phenol sulphonic acid-4 gms 2.0 Silver nitrate "gms-- 2.5 Mercurous nitrate (HgNOi2H:O)-- gms 3.5 Water -ccs A metal image can be obtained in the film thus obtained by the physical development described in Example I.
Upon comparison of physically-developed" images on films containing bismuth oxy-nitrate with images on films subjected to exactly the same treatments, but with the difference that a bath in nitric acid of 4% is substituted for the bath in the nitric bismuth nitrate solution, it is found that in all of the Examples I to IV above, the gradation value ('7) is decreased. This will be more clearly explained with reference to Table I which gives some comparative data obtained from experiments which we have made.
Table I Gradatlon value 0! images produced Treatment 0! film Film con Film free taining Bi of Bi Example I 3. l 0 Example IL 4. 0 6. 3 Example III 1 3.0 About 6 Example IV 4. l About 6 Example V (a) Bathing for about three minutes in a 1 n.
ammonia solution,
(b) Bathing for three minutes in 0.1 n. caustic soda lye,
(c) Allowed to remain for several hours in a closed drum above a concentrated ammonia solution.
For the three films receiving the treatments a, b, and c respectively, the further treatment is the same; namely, rinsing for about 15 minutes in running water, bathing .for about 15 minutes in distilled Water, blotting between filter paper, and drying in. ail.
For comparison several films (not subject to the treatments at, b, or 0) were rimed only in distilled water (a), and several films were bathed in 0.1 N. caustic soda lye, followed by rinsing in water and bathing in distilled water (e).
All of the films treated in the described manners were sensitized by means of the following manner described in Example I.
In the films containing zirconium the color of the metal image is somewhat bluish.
With such a series the following gradation values were found:
Table II Gradation Treatment value respect.
In contradistinction to films containing bismuth which are often opalescent. films containing zirconium are substantially as transparent as films that have not been treated. I
Example VI Two similar cellulose films were treated according to Example V treatment 0 and sensitized. Subsequently one of these films was bathed for about one minute in ethanol of 55% to which is added 0.1 part by volume of glycerol. After removing the adhering excess liquid, the film was dried in air. The films were then exposed in a similar manner. After physical development, it was found that the film subjected to the aftertreatment is softer than a film which was not treated; the gradation value being 2.0 and 3.4 respectively.
While we have described our invention with reference to certain applications and in connec-' aqueous solution, and means within said portionv to produce local variationsin the concentration of the diazonium compound and to reduce the gradation value of the light-sensitive system. said means comprising a colloidally-dispersed material which is substantially not dissolved by the developing solution during the formation of the image.
2. A light-sensitive material adapted to be physically-developed after exposure bythe application of a developing solution comprising a support of a transparent lyophile colloid of the type of regenerated cellulose and cellulose derivatives, a light-sensitive system within a portion of said support and comprising a diazonium com- I pound and a metal salt which is reducible to a metal in an aqueous solution, and means within said portion to produce. local variations in the concentration of the diazonium compound and to reduce the gradation value of the light-sensitive system, said means comprising a colloidallydispersed material which is substantially not dissolved by the developing solution during the formation of the image.
3. A light-sensitive material adapted to be physically-developed after exposure by the application of a developing solution comprising a support of transparent regenerated cellulose, a lightsensitive system within a portion of said support and comprising a diazonium compound and a metal salt which is reducible to a metal in an aqueous solution, and means within said portion to produce local variations in the concentration of the diazonium compound and to reduce the gradation value of the light-sensitive system, said means comprising a oolloidally-dispersed material which is substantially not dissolved by the developing solution during the formation of the image.
4. A light-sensitive material adapted to be physically-developed after exposure by the application of a developing solution comprising a support of a transparent cellulose derivative of the type of acetyl cellulose and gelatin material, a light-sensitive system within a portion of said support and comprising a diazonium compound and a metal salt which is reducible to a metal in an aqueous solution, and means within said portion to produce local variations in the concentration of the diazonium compound and to reduce. the gradation value of the light-sensitive system, said means comprising a colloidally-dispersed material'which is substantially not dissolved by the developing solution during the formation of the image.
5. A light-sensitive material adapted to be physically developed after exposure by the application of a developing solution comprising a support of a transparent lyophile colloid, a lightsensitive system within a portion of said support and comprising a diazonium compound and a metal salt which is reducible to a metal in an aqueous solution, and means within said portion to produce local variations in the concentration of the diazonium compound and to reduce the gradation value of the light-sensitive system, said means comprising colloidally-dispersed basic bismuth nitrate. I
6. A method of photo-chemically pro d ucing contrasts comprising the steps of placing a diazonium compound within a portion of a support of a transparent lyophile colloid to.form a lightsensitive system, incorporating within the said portion of the support to produce local variations in the concentration of the diazonium compounds coiloidally-dispersed material which is substantially not dissolved in the developing solution, selectively exposing the so-treated support to light, and physically developing the exposed support by applying to said portion a developing solution containing a metal salt reducible to a metal in an aqueous solution. a
. CORNELIS JOHANNES DIPPEL. ROELOF JAN HENDRIX ALINK. KLAAB JANNEB KEUNING.
US222536A 1937-08-09 1938-08-01 Light-sensitive material and method of making the same Expired - Lifetime US2183447A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEN0041062 1937-08-09

Publications (1)

Publication Number Publication Date
US2183447A true US2183447A (en) 1939-12-12

Family

ID=7348327

Family Applications (1)

Application Number Title Priority Date Filing Date
US222536A Expired - Lifetime US2183447A (en) 1937-08-09 1938-08-01 Light-sensitive material and method of making the same

Country Status (6)

Country Link
US (1) US2183447A (en)
BE (1) BE429591A (en)
CH (1) CH211505A (en)
FR (1) FR841911A (en)
GB (1) GB511816A (en)
NL (1) NL53832C (en)

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2416021A (en) * 1944-12-29 1947-02-18 Gen Aniline & Film Corp Light sensitive diazotype compositions and process
US2571671A (en) * 1946-01-18 1951-10-16 Hartford Nat Bank & Trust Co Process of producing photographic contrasts
US2571670A (en) * 1946-01-21 1951-10-16 Hartford Nat Bank & Trust Co Method of producing photographic contrasts
US2588218A (en) * 1946-06-01 1952-03-04 Hartford Nat Bank & Trust Co Method of drying photographic material
US2609295A (en) * 1947-10-27 1952-09-02 Hartford Nat Bank & Trust Co Process for discontinuously physically developing latent photographic images
US2618555A (en) * 1949-04-09 1952-11-18 Kalle & Co Ag Process for positive diazotype and negative metal reduction images and light-sensitive material therefor
US2733144A (en) * 1951-03-28 1956-01-31 Method of producing photographic
US2735773A (en) * 1951-03-27 1956-02-21 Method of producing a photographic
US2738272A (en) * 1950-07-25 1956-03-13 Hartford Nat Bank & Trust Co Photographic process
US2750292A (en) * 1950-05-26 1956-06-12 Hartford Nat Bank & Trust Co Process for producing colored photographic contrasts
US2764484A (en) * 1950-10-03 1956-09-25 Hartford Nat Bank & Trust Co Method of forming photographic images by physical developing
US2838398A (en) * 1951-03-27 1958-06-10 Philips Corp Method of producing a physically developable latent photographic image
US2923626A (en) * 1956-09-18 1960-02-02 Philips Corp Method of forming photographic images
US2929709A (en) * 1951-07-10 1960-03-22 Philips Corp Photographic process
US3409438A (en) * 1963-08-26 1968-11-05 Minnesota Mining & Mfg Photosensitive heat developable copysheet
US20140367613A1 (en) * 2011-12-22 2014-12-18 Gc Corporation Fluorescence imparting agent for ceramics

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2416021A (en) * 1944-12-29 1947-02-18 Gen Aniline & Film Corp Light sensitive diazotype compositions and process
US2571671A (en) * 1946-01-18 1951-10-16 Hartford Nat Bank & Trust Co Process of producing photographic contrasts
US2571670A (en) * 1946-01-21 1951-10-16 Hartford Nat Bank & Trust Co Method of producing photographic contrasts
US2588218A (en) * 1946-06-01 1952-03-04 Hartford Nat Bank & Trust Co Method of drying photographic material
US2609295A (en) * 1947-10-27 1952-09-02 Hartford Nat Bank & Trust Co Process for discontinuously physically developing latent photographic images
US2618555A (en) * 1949-04-09 1952-11-18 Kalle & Co Ag Process for positive diazotype and negative metal reduction images and light-sensitive material therefor
US2750292A (en) * 1950-05-26 1956-06-12 Hartford Nat Bank & Trust Co Process for producing colored photographic contrasts
US2738272A (en) * 1950-07-25 1956-03-13 Hartford Nat Bank & Trust Co Photographic process
US2764484A (en) * 1950-10-03 1956-09-25 Hartford Nat Bank & Trust Co Method of forming photographic images by physical developing
US2735773A (en) * 1951-03-27 1956-02-21 Method of producing a photographic
US2838398A (en) * 1951-03-27 1958-06-10 Philips Corp Method of producing a physically developable latent photographic image
US2733144A (en) * 1951-03-28 1956-01-31 Method of producing photographic
US2929709A (en) * 1951-07-10 1960-03-22 Philips Corp Photographic process
US2923626A (en) * 1956-09-18 1960-02-02 Philips Corp Method of forming photographic images
US3409438A (en) * 1963-08-26 1968-11-05 Minnesota Mining & Mfg Photosensitive heat developable copysheet
US20140367613A1 (en) * 2011-12-22 2014-12-18 Gc Corporation Fluorescence imparting agent for ceramics

Also Published As

Publication number Publication date
NL53832C (en)
BE429591A (en)
CH211505A (en) 1940-09-30
FR841911A (en) 1939-06-01
GB511816A (en) 1939-08-24

Similar Documents

Publication Publication Date Title
US2183447A (en) Light-sensitive material and method of making the same
US2665986A (en) Process of producing colored reversal images
US2740717A (en) Photographic transfer process
GB439005A (en) Improved methods of obtaining photographic contrasts by means of diazonium compounds and sensitive layers for use therein
US3730716A (en) Silver image stabilization with noble metal compounds and alpha,beta-enediol developer
US3466173A (en) Silver halide element containing a developer and aromatic sulfinic acid stabilizers
DE1547793A1 (en) Direct positive silver halide photographic emulsion
GB687751A (en) Process and material for the direct production of positive photographic images
DE1945408A1 (en) Process for making photographic images
US3656961A (en) Direct positive silver halide photographic light-sensitive elements
US3124458A (en) Direct positive photographic materials
US3615607A (en) Method of desensitizing light-sensitive silver halide photographic materials with cycloheptimidazole derivatives
US3821000A (en) Silver image stabilization with noble metal compounds and enediol developers
US2937945A (en) Process and photographic material for the direct production of positive photographicimages
US3674489A (en) Photographic image amplifying with copper ions
US3993490A (en) Direct positive photographic elements containing developers
US2952538A (en) Photographic process
US2584029A (en) Photographic silver transfer product and process, including a lead salt
US2929709A (en) Photographic process
US2689792A (en) Process for producing and developing light-sensitive photographic layers
US3843363A (en) Photographic developer with cuprous amine complex
US2696439A (en) Photographic stabilization process
US3021212A (en) Developers for photographic reversal processes
US3053657A (en) Photographic silver halide diffusion transfer process
US2733144A (en) Method of producing photographic