US3772017A - Diazo-type developing process - Google Patents

Diazo-type developing process Download PDF

Info

Publication number
US3772017A
US3772017A US00109547A US3772017DA US3772017A US 3772017 A US3772017 A US 3772017A US 00109547 A US00109547 A US 00109547A US 3772017D A US3772017D A US 3772017DA US 3772017 A US3772017 A US 3772017A
Authority
US
United States
Prior art keywords
diazo
light
grams
image
compound
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
US00109547A
Inventor
M Reichel
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.)
Kalle GmbH and Co KG
Original Assignee
Kalle GmbH and Co KG
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 Kalle GmbH and Co KG filed Critical Kalle GmbH and Co KG
Application granted granted Critical
Publication of US3772017A publication Critical patent/US3772017A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • G03C5/18—Diazo-type processes, e.g. thermal development, or agents therefor

Definitions

  • Diazo-type imaging processes have long been known and ordinarily employ diazonium compounds which are light-sensitive and readily decomposable by exposure to actinic radiation, generally ultraviolet light. Image-wise exposure of light-sensitive diazonium materials effects the formation of a diazonium compound image which may subsequently be coupled with azo components to form distinctly visible dye images.
  • Two diazo-type processes in common use include the one-component system which utilizes sheet material bearing only the light sensitive diazonium compound, the azo coupler component being applied subsequent to light exposure in a developing solution.
  • a disadvantage inherent in the usual one-component system arises from the fact that the developing solution contains alkaline ingredients conductive to the coupling reaction. The inherent alkalinity, however, renders the developing solution particularly susceptible to aerial oxidation, thereby reducing its useful life.
  • the second process includes both the light-sensitive diazonium compound and the azo. dye coupler together in the light-sensitive material along with acid stabilizers which prevent premature dye-forming coupling. Subsequent to light exposure the material is contacted with a developing medium of high alkalinity, usually moist ammonia gas, to effect the dye-forming coupling reaction.
  • a developing medium of high alkalinity usually moist ammonia gas
  • diazo-type compositions comprising diazo sulfonate compounds which, in general, are light-sensitive and possess the additional property of being capable of forming distinctive azo dyes when heated in the presence of azo dye coupler compounds.
  • a system employing diazo sulfonate compositions is described in U.S. Pat. No. 2,217,189.
  • the various disadvantages encountered heretofore with diazo-type materials and processes are avoided by employing in a diazo-type process a light-sensitive material which utilizes the more highly light-sensitive diazonium compounds, and developing the characteristic azo dye image subsequent to light exposure by applying a developer solution which comprises an azo coupler component and sufficient amount of a sulfite compound to convert the image-wise disposed diazonium compound to the corresponding diazo sulfonate compound, and heating the resulting sheet to thereby effect dyeforming coupling of the diazo sulfonate with the azo coupler component.
  • a developer solution which comprises an azo coupler component and sufficient amount of a sulfite compound to convert the image-wise disposed diazonium compound to the corresponding diazo sulfonate compound, and heating the resulting sheet to thereby effect dyeforming coupling of the diazo sulfonate with the azo coupler component.
  • the present invention additionally provides a greater choice in the available light-sensitive materials of practical imaging'speed, a prolonged shelf life and stability of diazo-type materials which are devoid of the diazo/- coupler component combination, and a broad scope of color combinations available through the free selection of both the diazonium and azo coupler components; and further avoids the dangers and discomforts associated with the use of noxious, gaseous developers, such as ammonia.
  • the light-sensitive materials useful in the present invention include sheet-like supports such as paper, film or the likebearing a coating of a composition which comprises at least one light-sensitive diazonium compound.
  • Such materials may be the commonly employed one-component or two-component diazo-type sheets, however, it is preferred to employ the one-component material to take advantage of the greater storage stability of compositions which are essentially devoid of the azo coupler component.
  • the composition may include the usual diazo-type composition adjuncts such as buffers of aminoacetic acid; stabilizers such as 1, 3, -trisulfonic acid; napthalene-l ,S-disulfonic acid; naphthalene-2,7-dissulfonic acid and their water soluble salts; antioxidants such as thiourea; metal salts such as aluminumsulfate; and binders such as gelatin, gum
  • Diazonium compounds which are useful in the present invention are those commonly employed in oneor two-component diazo-type systems, in particular the benzene diazonium salts which are substituted in the benzene nucleus at a position para to the diazo group with any of a tertiary amino, acylamino, arylamino, alkoxy, alkylmercapto, arylmercapto groups, a halogen atom, or a heterocyclic substituent.
  • the benezene nucleus of these'diazonium compounds may additionally be substituted in the 2, 3, 2 and 3, or 2 and 5 positions with any of an alkyl, alkoxy, aryloxy, alkylmercapto, or arylmercapto group, or a halogen atom.
  • diazonium compounds include 4-Ethoxy-benzene diazonium-; 3,4-Diethoxybenzenediazonium-; 4-Chloro 2,5-dimethoxybenzenediazonium-; benzenediazonium-;
  • anions such as chlorides, sulfates and the like may be employed to form the useful salts of the various diazonium compounds.
  • the light-sensitive materials are prepared in the usual manner by combining the diazonium compound with the selected adjuncts in an appropriate solvent or dispersion and coating the mixture onto selected supports such as paper, cloth, metallic foils, transparent papers and films such as cellulose acetate, polyester or polycarbonate sheets, and drying the resulting coatings.
  • selected supports such as paper, cloth, metallic foils, transparent papers and films such as cellulose acetate, polyester or polycarbonate sheets, and drying the resulting coatings.
  • the preparation of the light-sensitive material does not differ significantly from that of oneor twocomponent diazo-type materials heretofore produced; in fact, commercial products of this type may be employed in the present process.
  • the developer solution employed in the process of the present invention includes any of the known rapidcoupling azo components found particularly useful in the common one-component moist developing diazotype systems.
  • azo coupler components include, for example, resorcinol; phloroglucinol; N-phenylpyrazolone-(S); acetoacetic acid amide; 2, 3 dihydroxy-naphthalene; and the like.
  • the developer solution includes a substantial amount of a sulfite salt, such as sodium sulfite.
  • a sulfite salt such as sodium sulfite.
  • Application of a layer or thin film of the developer solution to a light-exposed sheet of the diazo-type material directly forms, by the action of the sulfite, a diazo-N-sulfonate disposed in image-wise fashion according to the diazonium compound remaining in the sheet material after exposure. While the sheet remains moistened at its surface with the developer solution, the sheet material is heated, such as by passing in contact with rollers maintained at a temperature of between about 130 and 150 C.
  • the effect of heating the material is to convert the diazo-N- sulfonate compound into an active coupling form whereupon immediate dye-forming coupling with the azo coupler compound takes place with formation of the distinctive dye image.
  • Concurrently the sheet is dried and the imaged material is ready for use without further fixing, or aeration which is often required, particularly with ammonia-developed two-component diazo-type systems.
  • Example 1 A paper sheet previously coated with a solution of zinc acetate was coated in the usual manner with an aqueous solution containing, in one liter, the following compounds:
  • EXAMPLE 2 A common diazo-type paper base sheet was precoated with zinc acetate as in Example 1 and then coated with an aqueous solution containing, in one liter:
  • EXAMPLE 3 The pre-coated paper of Example 2 was coated with an aqueous solution containing in one liter:
  • the moistened sheet material was developed with heat as described in Example 1 to yield a deep red dye image.
  • Substitution of 8.0 grams 2,3-di-hydroxynaphthalene or 7.5 grams phloroglucinol for the pyrazolone compound of Example 3 yielded upon development respectively blue and deep blue-violet images on white backgrounds.
  • An imaging process comprising:
  • EXAMPLE 4 a forming on a suitable support a coating of a com- A cellulose acetate film, superficially hydrolysed to iti comprising; Provide a more Coatable hydrophillic Surface, was 1. a light-sensitive benzene diazonium compound, coated with an aqueous solution containing, in one Ii- 5 2 aminoacetic acid, d

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
  • Heat Sensitive Colour Forming Recording (AREA)

Abstract

A diazo-type developing process, for light sensitive imaging material comprising a diazonium compound, employs a developer solution including an azo coupler compound and sodium sulfite. Contacting the exposed diazo-type material with the solution converts the image-wise disposed light-sensitive diagzonium compound to a diazo sulfonate, and subsequent heating effects development of an azo dye image while drying the sheet. The developer solution is resistant to oxidation and exhibits an extended useful life.

Description

United States Patent [191 Reichel DIAZO-TYPE DEVELOPING PROCESS [75] Inventor: Maximilian Karl Reichel,
Wiesbaden-Bierbrich, Germany [73] Assignee: Kalle Aktiengesellschatt,
Wiesbaden-Biebrich, Germany [22] Filed: Jan. 25, 1971 [21] Appl. No.: 109,547
[30] Foreign Application Priority Data Jan. 27, 1970 Germany P 20 03 542.1
[52] US. Cl. 96/49 [51] Int. Cl G036 5/18, G030 5/34 [58] Field of Search 96/49.75, 91; 250/651; ll7/36.7, 36.8, 36.9
[56] References Cited UNITED STATES PATENTS 2,217,189 10/1940 Sus 96/49 3,431,109 3/1969 Bialczak 96/49 3,309,200 3/1967 Berman et a1. 96/49 2,113,944 3/1968 Leuch 96/49 2,205,991 6/1940 Neugebauer et a1... 96/49 3,224,878 12/1965 Klimkowski et al. 96/49 3,164,469 1/1965 Behmenburg et a1 96/49 2,789,904 4/1957 Benbrook et a1. 96/49 2,680,062 6/1954 Sus 96/49 1 Nov. 13, 1973 11/1954 Sus 96/49 X 7/1934 Dl-lauterive 96/49 OTHER PUBLICATIONS Kosar, J.; Photographic Science & Engineering, Vol. 5, No. 4, July-August 1961, p. 239-243. Dinaburg, M. S.; Photosensitive Diazo Cpds, The Focal Press, 1964, p. 13-17, 80, 81, 93, 123 and 152-154.
Kosar, 1.; Light-Sensitive Systems, J. Wiley & Sons, 1965, p. 266, 269-270 and 291.
Primary Examiner-Charles L. Bowers, Jr. Attorney-J. Russell .luten, Peter F. Willig, Lionel M. White and Milford A. J uten [57] ABSTRACT 2 Claims, No Drawings DIAZO-TYPE DEVELOPING PROCESS BACKGROUND OF THE INVENTION Diazo-type imaging processes have long been known and ordinarily employ diazonium compounds which are light-sensitive and readily decomposable by exposure to actinic radiation, generally ultraviolet light. Image-wise exposure of light-sensitive diazonium materials effects the formation of a diazonium compound image which may subsequently be coupled with azo components to form distinctly visible dye images.
Two diazo-type processes in common use include the one-component system which utilizes sheet material bearing only the light sensitive diazonium compound, the azo coupler component being applied subsequent to light exposure in a developing solution. A disadvantage inherent in the usual one-component system arises from the fact that the developing solution contains alkaline ingredients conductive to the coupling reaction. The inherent alkalinity, however, renders the developing solution particularly susceptible to aerial oxidation, thereby reducing its useful life.
The second process, a two-component diazo-type system, includes both the light-sensitive diazonium compound and the azo. dye coupler together in the light-sensitive material along with acid stabilizers which prevent premature dye-forming coupling. Subsequent to light exposure the material is contacted with a developing medium of high alkalinity, usually moist ammonia gas, to effect the dye-forming coupling reaction. An obvious disadvantage of the two-component diazo-type system arises from the pungent and irritating nature of the gaseous ammonia developing agent.
Attempts have been made to supplant the disadvantageous gaseous and moist developing diazo-type systems with materials and processes which employ heat alone as a means of effecting azo dye image formation. Among such heat-developing materials are diazo-type compositions comprising diazo sulfonate compounds which, in general, are light-sensitive and possess the additional property of being capable of forming distinctive azo dyes when heated in the presence of azo dye coupler compounds. A system employing diazo sulfonate compositions is described in U.S. Pat. No. 2,217,189.
Although the disadvantages of the usual-oneor twocomponent diazo-type systems are avoided through the use of diazo sulfonate materials, additional disadvantages arise, particularly in the loss of light sensitivity as compared with materials employing diazonium compounds. The preparation of diazo sulfonate coating materials which possessed a practical degree of light sensitivity therefore was limited in the scope of useful light sensitive components and required close attention to the type of diazo compound employed in order to achieve acceptable results.
In addition to the inherent lower level of light sensitivity, the necessity of combining diazo sulfonate compounds with azo dye coupler components in a composition proved additionally disadvantageous due to the uncontrollable pre-coupling and instability of the composition. Attempts to improve the shelf life of these materials included the addition of various stabilizing materials such as described in U.S. Pat. No. 2,429,249 and U.S. Pat. No. 2,694,009. Incorporation of such stabilizers in the light-sensitive compositions represented,
however, a further compromise to the light sensitivity of the material.
SUMMARY OF THE INVENTION According to the present invention the various disadvantages encountered heretofore with diazo-type materials and processes are avoided by employing in a diazo-type process a light-sensitive material which utilizes the more highly light-sensitive diazonium compounds, and developing the characteristic azo dye image subsequent to light exposure by applying a developer solution which comprises an azo coupler component and sufficient amount of a sulfite compound to convert the image-wise disposed diazonium compound to the corresponding diazo sulfonate compound, and heating the resulting sheet to thereby effect dyeforming coupling of the diazo sulfonate with the azo coupler component. As a result of the present invention, advantage is taken of the high light sensitivity of diazonium compounds, the greater heat stability of diazo sulfonate compounds, and the resistance of the generally acidic developer solution to aerial oxidation.
The present invention additionally provides a greater choice in the available light-sensitive materials of practical imaging'speed, a prolonged shelf life and stability of diazo-type materials which are devoid of the diazo/- coupler component combination, and a broad scope of color combinations available through the free selection of both the diazonium and azo coupler components; and further avoids the dangers and discomforts associated with the use of noxious, gaseous developers, such as ammonia.
DESCRIPTION OF THE INVENTION The light-sensitive materials useful in the present invention include sheet-like supports such as paper, film or the likebearing a coating of a composition which comprises at least one light-sensitive diazonium compound. Such materials may be the commonly employed one-component or two-component diazo-type sheets, however, it is preferred to employ the one-component material to take advantage of the greater storage stability of compositions which are essentially devoid of the azo coupler component. In addition to the lightsensitive diazonium compound, the composition may include the usual diazo-type composition adjuncts such as buffers of aminoacetic acid; stabilizers such as 1, 3, -trisulfonic acid; napthalene-l ,S-disulfonic acid; naphthalene-2,7-dissulfonic acid and their water soluble salts; antioxidants such as thiourea; metal salts such as aluminumsulfate; and binders such as gelatin, gum
arabic, synthetic resins, silica dispersions and the like.
Diazonium compounds which are useful in the present invention are those commonly employed in oneor two-component diazo-type systems, in particular the benzene diazonium salts which are substituted in the benzene nucleus at a position para to the diazo group with any of a tertiary amino, acylamino, arylamino, alkoxy, alkylmercapto, arylmercapto groups, a halogen atom, or a heterocyclic substituent. The benezene nucleus of these'diazonium compounds may additionally be substituted in the 2, 3, 2 and 3, or 2 and 5 positions with any of an alkyl, alkoxy, aryloxy, alkylmercapto, or arylmercapto group, or a halogen atom.
Some particularly useful diazonium compounds include 4-Ethoxy-benzene diazonium-; 3,4-Diethoxybenzenediazonium-; 4-Chloro 2,5-dimethoxybenzenediazonium-; benzenediazonium-;
4-Acetylamino- 4-Benzoylamino-2,5 -diethoxymethoxy-benzenediazonium-; 2-Phenylmercapto-4- ethylmercapto-S-ethoxy-benzenediazonium-; N-ethylcarbazol-3-diazonium-; 4-Dipropylaminobenzenediazonium-; 2-Methyl-4-diethylamino-benzene-diazonium-; 4-Morpholino-2,S-dibutoxy benzenediazonium-; and 3-Methoxy-4-dipropylaminobenzenediazonium salts.
The usual types of anions such as chlorides, sulfates and the like may be employed to form the useful salts of the various diazonium compounds.
The light-sensitive materials are prepared in the usual manner by combining the diazonium compound with the selected adjuncts in an appropriate solvent or dispersion and coating the mixture onto selected supports such as paper, cloth, metallic foils, transparent papers and films such as cellulose acetate, polyester or polycarbonate sheets, and drying the resulting coatings. Thus the preparation of the light-sensitive material does not differ significantly from that of oneor twocomponent diazo-type materials heretofore produced; in fact, commercial products of this type may be employed in the present process.
The developer solution employed in the process of the present invention includes any of the known rapidcoupling azo components found particularly useful in the common one-component moist developing diazotype systems. Such azo coupler components include, for example, resorcinol; phloroglucinol; N-phenylpyrazolone-(S); acetoacetic acid amide; 2, 3 dihydroxy-naphthalene; and the like.
In addition to the azo coupler component, the developer solution includes a substantial amount of a sulfite salt, such as sodium sulfite. Application of a layer or thin film of the developer solution to a light-exposed sheet of the diazo-type material directly forms, by the action of the sulfite, a diazo-N-sulfonate disposed in image-wise fashion according to the diazonium compound remaining in the sheet material after exposure. While the sheet remains moistened at its surface with the developer solution, the sheet material is heated, such as by passing in contact with rollers maintained at a temperature of between about 130 and 150 C. The effect of heating the material is to convert the diazo-N- sulfonate compound into an active coupling form whereupon immediate dye-forming coupling with the azo coupler compound takes place with formation of the distinctive dye image. Concurrently the sheet is dried and the imaged material is ready for use without further fixing, or aeration which is often required, particularly with ammonia-developed two-component diazo-type systems.
PREFERRED EMBODIMENTS Example 1 A paper sheet previously coated with a solution of zinc acetate was coated in the usual manner with an aqueous solution containing, in one liter, the following compounds:
24.6 grams 4-phenylamino-benzene diazonium sulfate 20.0 grams aminoacetic acid 20.0 grams thiourea Subsequent to drying, the resulting sheet was exposed under an original in an ordinary diazo-type copying device having a ultraviolet light source and the remaining diazo composition was lightly moistened with a developer solution containing, in one liter of water, the following compounds:
50.0 grams sodium sulfite 7.5 grams 2,3-dihydroxy-naphthalene 30.8 grams magnesium salicilate 20.0 grams sodium benzoate.
While the material remained moistened with the developer solution, it was heated by passing through rollers at a temperature of between about and l50 C There was immediately developed a deep blue-violet image on a white background.
Substitution in the developing solution of 10 grams of resorcino] for the 2,3-dihydroxy-naphthalenc yielded a deep brown-red image on a white background when the exposed sheet material was treated in the foregoing manner.
EXAMPLE 2 A common diazo-type paper base sheet was precoated with zinc acetate as in Example 1 and then coated with an aqueous solution containing, in one liter:
22.5 grams N-ethyl-carbazol-3-diazonium chloridezinc chloride 20.0 grams aminoacetic acid 40.0 grams thiourea The dried sheet was image-wise exposed under an original in the usual manner and was moistened with an aqueous solution containing, in one liter:
50.0 grams sodium sulfite 10.0 grams resorcinol 30.0 grams magnesium salicilate 20.0 grams sodium benzoate The moistened sheet was developed by heating as in Example 1, yielding a deep red brown dye image.
EXAMPLE 3 The pre-coated paper of Example 2 was coated with an aqueous solution containing in one liter:
24.0 grams 4-dipropylamino-benzene diazonium chloride zinc chloride 20.0 grams aminoacetic acid 400 grams thiourea The dried sheet was exposed under an original, as previously described, and subsequently moistened with an aqueous solution containing, in one liter:
50.0 grams sodium sulfite 8.0 grams l-phenyl-3 -methyl-pyrazolone-(5) 30.0 grams magnesium salicilate 20.0 grams sodium benzoate.
The moistened sheet material was developed with heat as described in Example 1 to yield a deep red dye image. Substitution of 8.0 grams 2,3-di-hydroxynaphthalene or 7.5 grams phloroglucinol for the pyrazolone compound of Example 3 yielded upon development respectively blue and deep blue-violet images on white backgrounds.
1. An imaging process comprising:
EXAMPLE 4 a. forming on a suitable support a coating of a com- A cellulose acetate film, superficially hydrolysed to iti comprising; Provide a more Coatable hydrophillic Surface, was 1. a light-sensitive benzene diazonium compound, coated with an aqueous solution containing, in one Ii- 5 2 aminoacetic acid, d
ter:
24.0 grams 2-methyl-4-diethylamino-benzene diazonium chloride zinc chloride 20.0 grams aminoacetic acid 40.0 grams thiourea 10 The dried sheet was exposed under an original as in the previous examples, and then moistened at the coated surface with an aqueous solution containing, in
3. thiourea;
b exposing said coating imagewise to light thereby forming an image-wise disposition of said composition on said support;
c. moistening said image-wise disposed composition with an acidic solution comprising:
1. an azo coupler compound normally coupling with said diazonium compound under alkaline one liter:
50.0 grams Sodium Sulfite conditions to form an azo dye, and 75 grams phloroglucinol 2. an alkali sulfite salt, and 30 grams magnesium salicylate d. heating said moistened composition in excess of 2() grams di benzoate about 100 C, thereby effecting formation of an azo The moistened sheet was heated, as in Example I, y imageand developed a deep blue-violet colored image on a 2- An imaging proc ss according to claim 1 wherein transparent background. said sulfite salt is sodium sulfite.
I claim:

Claims (4)

  1. 2. aminoacetic acid, and
  2. 2. an alkali sulfite salt, and d. heating said moistened composition in excess of about 100* C, thereby effecting formation of an azo dye image.
  3. 2. An imaging process according to claim 1 wherein said sulfite salt is sodium sulfite.
  4. 3. thiourea; b. exposing said coating imagewise to light thereby forming an image-wise disposition of said composition on said support; c. moistening said image-wise disposed composition with an acidic solution comprising:
US00109547A 1970-01-27 1971-01-25 Diazo-type developing process Expired - Lifetime US3772017A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19702003542 DE2003542A1 (en) 1970-01-27 1970-01-27 Diazotype process

Publications (1)

Publication Number Publication Date
US3772017A true US3772017A (en) 1973-11-13

Family

ID=5760600

Family Applications (1)

Application Number Title Priority Date Filing Date
US00109547A Expired - Lifetime US3772017A (en) 1970-01-27 1971-01-25 Diazo-type developing process

Country Status (3)

Country Link
US (1) US3772017A (en)
CA (1) CA948467A (en)
DE (1) DE2003542A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4382262A (en) * 1981-03-23 1983-05-03 Joseph Savit Multicolor jet printing

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1966755A (en) * 1931-11-09 1934-07-17 Kalle & Co Ag Process of preparing diazo-types
US2113944A (en) * 1933-09-11 1938-04-12 Dietzgen Eugene Co Production of photographic diazotype prints
US2205991A (en) * 1935-12-28 1940-06-25 Kalle & Co Ag Diazotype process
US2217189A (en) * 1938-12-05 1940-10-08 Kalle & Co Ag Process of preparing photographic prints
US2680062A (en) * 1949-07-23 1954-06-01 Keuffel & Esser Co Process for the production of azo dyestuff images
US2694009A (en) * 1948-10-01 1954-11-09 Keuffel & Esser Co Diazo-n-sulfonate light-sensitive material
US2789904A (en) * 1953-09-17 1957-04-23 Gen Aniline & Film Corp Diazo print process
US3164469A (en) * 1960-03-04 1965-01-05 Keuffel & Esser Co One-component diazo process
US3224878A (en) * 1961-12-01 1965-12-21 Dietzgen Co Eugene Thermographic diazotype reproduction material, method of making and method of using
US3309200A (en) * 1963-06-03 1967-03-14 Itek Corp Data reproduction process
US3431109A (en) * 1964-10-16 1969-03-04 Addressograph Multigraph Heat sensitive diazotype materials

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1966755A (en) * 1931-11-09 1934-07-17 Kalle & Co Ag Process of preparing diazo-types
US2113944A (en) * 1933-09-11 1938-04-12 Dietzgen Eugene Co Production of photographic diazotype prints
US2205991A (en) * 1935-12-28 1940-06-25 Kalle & Co Ag Diazotype process
US2217189A (en) * 1938-12-05 1940-10-08 Kalle & Co Ag Process of preparing photographic prints
US2694009A (en) * 1948-10-01 1954-11-09 Keuffel & Esser Co Diazo-n-sulfonate light-sensitive material
US2680062A (en) * 1949-07-23 1954-06-01 Keuffel & Esser Co Process for the production of azo dyestuff images
US2789904A (en) * 1953-09-17 1957-04-23 Gen Aniline & Film Corp Diazo print process
US3164469A (en) * 1960-03-04 1965-01-05 Keuffel & Esser Co One-component diazo process
US3224878A (en) * 1961-12-01 1965-12-21 Dietzgen Co Eugene Thermographic diazotype reproduction material, method of making and method of using
US3309200A (en) * 1963-06-03 1967-03-14 Itek Corp Data reproduction process
US3431109A (en) * 1964-10-16 1969-03-04 Addressograph Multigraph Heat sensitive diazotype materials

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
Dinaburg, M. S.; Photosensitive Diazo Cpds, The Focal Press, 1964, p. 13 17, 80, 81, 93, 123 and 152 154. *
Kosar, J.; Light Sensitive Systems, J. Wiley & Sons, 1965, p. 266, 269 270 and 291. *
Kosar, J.; Photographic Science & Engineering, Vol. 5, No. 4, July August 1961, p. 239 243. *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4382262A (en) * 1981-03-23 1983-05-03 Joseph Savit Multicolor jet printing

Also Published As

Publication number Publication date
DE2003542A1 (en) 1971-08-12
CA948467A (en) 1974-06-04

Similar Documents

Publication Publication Date Title
US3764329A (en) Heat activated dry silver
US2246425A (en) Production of diazotype reflex copies
US2429249A (en) Stabilized aryl diazo-n-sulfonate light-sensitive material
US3887376A (en) Photographic elements, compositions and processes
US3479183A (en) Negative-working diazosulfonate reproduction process
US3772017A (en) Diazo-type developing process
US2552354A (en) Diazotype layers containing diazos of n-(2-hydroxypropyl)-phenylenediamines
US2432549A (en) Diazotype layers containing thiourea derivatives of hydroxy benzene
GB711390A (en) Improvements in or relating to photographic light-sensitive diazotype materials
US3622326A (en) Diazotype light-sensitive copying papers intended for wet development and for use in the preparation of intermediates
US3653903A (en) Diazo-type multicolor reproduction process
US3573051A (en) Two-component diazotype composition
US2542560A (en) Diazotypes on plastic surfaced carrier containing 5,5' diresorcinol
US3379531A (en) Two-component heat developing diazotypes
US3389996A (en) Two-component heat developable diazotypes
US3442650A (en) Diazonium compounds and diazotype materials containing them
US2495827A (en) Diazotype materials stabilized with an alpha-alkylidene-polymethylene dicarboxylic acid
US3442652A (en) Diazonium compounds and diazotype material
US3389995A (en) Two-component heat developable diazotypes containing amidine compounds
US3512978A (en) Diazosulfonate composition,copying material,and method of use
US3719491A (en) Diazo-type reproduction process
US3442651A (en) Diazonium compounds and diazotype materials containing them
US4055425A (en) Diazotype material and graphic reproduction processes employing the same
US3459550A (en) Diazotype material
US2531004A (en) Acetonitriles as azo components in diazotypes