US3418469A - Diazo reproduction - Google Patents

Diazo reproduction Download PDF

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Publication number
US3418469A
US3418469A US445704A US44570465A US3418469A US 3418469 A US3418469 A US 3418469A US 445704 A US445704 A US 445704A US 44570465 A US44570465 A US 44570465A US 3418469 A US3418469 A US 3418469A
Authority
US
United States
Prior art keywords
diazo
layer
particles
reproduction
discrete
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
US445704A
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English (en)
Inventor
Robert M Gold
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.)
Keuffel and Esser Co
Original Assignee
Keuffel and Esser Co
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 Keuffel and Esser Co filed Critical Keuffel and Esser Co
Priority to US445704A priority Critical patent/US3418469A/en
Priority to DE19661572076 priority patent/DE1572076A1/de
Priority to BE678993D priority patent/BE678993A/xx
Priority to AT320066A priority patent/AT277752B/de
Priority to SE04502/66A priority patent/SE326102B/xx
Priority to NL6604532A priority patent/NL6604532A/xx
Priority to FR56426A priority patent/FR1473770A/fr
Priority to GB15108/66A priority patent/GB1134943A/en
Application granted granted Critical
Publication of US3418469A publication Critical patent/US3418469A/en
Assigned to CHASE MANHATTAN BANK, N.A. THE; A NATIONAL BANKING ASSOCIATION, CONTINENTAL ILLINOIS NATIONAL BANK & TRUST CO., OF CHICAGO, A NATIONAL BANKING ASSOCIATION, BANK OF CALIFORNIA N.A. THE; A NATIONAL BANKING ASSOCIATION, SECURITY NATIONAL BANK, A NATIONAL BANKING ASSOCIATION FOR ITSELF AND AS AGENT FOR CITIBANK, N.A. A NATIONAL BANKING ASSOCIATION, CHEMICAL BANK, A BANKING INSTITUTION OF reassignment CHASE MANHATTAN BANK, N.A. THE; A NATIONAL BANKING ASSOCIATION SECURITY INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KEUFFEL & ESSER COMPANY A.N.J. CORP
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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

Definitions

  • a method for image formation on diazotype material includes the use of developable diazotype composition having an outer coating of a layer of discrete solid particles of a thermoplastic polymeric material which is ordinarily permeable to diazotype developing fluids, but when heated will form a coalesced impermeable film.
  • a developer fluid such as ammonia vapors or an alkaline solution of azo dye coupler
  • the present invention relates to diazo reproduction and refers more particularly to materials and methods for making diazo reproductions.
  • diazo materials are exposed to actinic radiation through a transparent or translucent original, thereby destroying the light-sensitive diazo compound in the exposed areas.
  • the undecomposed diazo compound is then combined with a coupling component in the presence of an alkali to form a dye. It is not presently possible to copy two-sided printed materials or graphic information on opaque bases by this procedure, nor is it possible to make a reversal copy by this procedure.
  • one object of the present invention is to provide materials and methods for making diazo reproductions, which overcome the disadvantages of the prior art.
  • Another object is to provide materials and methods for copying opaque and two-sided originals.
  • Another object is to provide materials and methods for making direct and reversal copies.
  • Another object is to provide methods for making diazo reproductions by the reflex technique.
  • Another object is to provide methods for making diazo transparencies without ultraviolet radiation.
  • Another object is to provide methods for making diazo intermediates from originals having printed matter on both sides.
  • the objects of the present invention may be realized by impressing an image on a diazo material overcoated with a layer of discrete coalesceable thermoplastic particles, by means of infrared radiation or ultraviolet radiation, and developing the image by means of ammonia vapors or a liquid developer.
  • the diazo material may be of the dry-developing variety or the semi-moist variety. In the dry-developing type, the diazo compound and the coupler are on the same support. In the semi-moist type, only the diazo compound is on the support; the coupler is in the aqueous developer.
  • the discrete coalesceable thermoplastic particles may also be coated together with the diazo compound.
  • the diazo material preferably comprises a diazo layer on a support which is substantially vapor and liquid-impervious. Paper may be used but plastic films are better.
  • a conventional dry-developing diazo material was overcoated with 3,418,469 Patented Dec. 24, 1968 a discontinuous layer of discrete coalesceable thermoplastic latex particles which coalesce above a given temperature.
  • the uniform, discontinuous layer was substantially transparent except for a slight haze which was barely visible.
  • the discontinuous layer was permeable to vapors and liquids.
  • the resulting sheet was used in a normal manner by contact exposure to ultraviolet radiation which decomposed the diazo compound in the light-struck areas and by development in ammonia vapors to produce a positive reproduction of good quality.
  • thermographic methods coupled with retention of the original conventional methods.
  • Thermal imaging may take place in a thermographic copying machine using an original with infrared-absorbing graphics.
  • the thermal exposure coalesces the latex particles in the image areas so that the particles adhere to each other and to the support in these areas.
  • the coalesced particles thus form a vapor barrier or mask that prevents development in heated areas while the uncoalesced particles permit coupling in the uu heated areas.
  • Development with ammonia produces a reversal copy of the original.
  • Subsequent uniform exposure to ultraviolet radiation stabilizes the image.
  • Exposure in the thermoprinting machine may be either by front-printing or back-printing.
  • the former permits copying two-sided or opaque originals.
  • Thermographic and photographic exposure techniques may be combined in any sequence to obtain composite copies of two or more originals.
  • the film substrate prevents ammonia permeation through the support to the underlying diazo layer, but paper and cloth substrates were still suitable for producing excellent reproductions.
  • a barrier coating of ammonia-impermeable polymer may be used.
  • a semi-moist diazo material was also used.
  • the sensitized layer was overcoated with the latex and used for photographic or thermographic copying to give positives, negatives, or combinations of both.
  • Development in the semi-moist developer proceeds normally for the ultra-violet-exposed copy, since the uncoalesced particles permit penetration of the developer into the sensitized layer.
  • Another example of this invention employs a developing sheet which releases alkali vapors upon heating.
  • the alkali-releasing temperature is below the particle-coalescing temperature to prevent serious image degradation.
  • the diazo material was placed in intimate contact with the alkali-releasing sheet with the particle layer in contact with the alkali-releasing sheet.
  • the composite was then passed through a heating machine which heats the paper to the alkali-releasing temperature.
  • an infrared-absorbing layer on the alkali sheet permits development by infrared radiation in a thermographic machine.
  • Suitable supports for the diazo layer were paper, film, cloth and similar bases. Where the support is transparent, the reproduction may be used as a transparency for projection purposes or as an intermediate for further reproduction.
  • photosensitive diazo compounds were 4-diethyl-amino-benzene diazonium borofluoride; 2,5-dimethoxy-4-morpholino-benzene diazonium borofluoride; 2,5 diethoxy-4-morpholino-benzene-diazonium borofluoride; 4 ethylbenzylamino benzene diazonium chloride; and mixtures thereof.
  • Other photosensitive diazonium compounds may be used.
  • Couplers were 2,4-dihydroxy-benzamide; 1-methyl-3-hydroxy-4-acetylamido-benzene; 3-hydroxy-2- naphthoic acid ethanolamide hydrochloride; diresorcinol sulfide; 4 bromo 3,5 dihydroxy benzoic acid amide; resorcinol; (2 hydroxy 4 methyl)-beta-pheny1-glutaric acid; 3-hydroxy-2-naphtholic acid ethylene-diamine amide hydrochloride; and mixtures thereof.
  • Other couplers may also be used.
  • Some suitable latexes were Rhoplex B-85 acrylic resin latex, Vinac WR- polyvinyl acetate emulsion, poly- EM non-ionic polyethylene emulsion, emulsion M polystyrene emulsion, Poly-EM11 anionic polyethylene emulsion.
  • the latexes were diluted to 1 to 10 percent by volume for coating purposes.
  • the particles were discrete when coated but were coalesced by the application of heat.
  • the layer of discrete particles is permeable to ammonia and to aqueous developer, but the coalesced particles are impervious to ammonia and to aqueous developer.
  • diazo material may be used as the starting material. It is coated with the layer of discrete coalesceable thermoplastic particles in a thin and transparent layer. In fact, the layer is barely discernible except as a slight haze on transparent supports.
  • a diazo reproduction material consisting essentially of:
  • a substantially fluid-impermeable support a layer of light-sensitive diazotype composition coated on said support, said composition comprising a light-sensitive diazonium compound capable of forming a dye with azo coupler compound;
  • a diazo reproduction material consisting essentially of:
  • a substantially fluid-impermeable support a layer of light-sensitive diazotype composition coated on said support, said composition comprising a light-sensitive diazonium compound and an azo coupler compound capable of forming a dye with said diazonium compound;
  • a diazo reproduction material according to claim 1 wherein said permeable layer consists essentially of discrete, coalesceable, thermoplastic particles of polyvinyl acetate.
  • a method of image reproduction comprising:
  • a developer fluid capable of promoting the formation of an azo dye in said diazotype composition, whereby said developer fluid penetrates the permeable areas of said polymer particle layer and effects dye formation in those portions of said diazotype composition immediately underlying said permeable areas.
  • said developer fluid comprises an alkaline solution of an azo coupler compound.
  • a method of image reproduction according to claim 7 including a further fixing step, after the application of developer, comprising exposing said material to ultraviolet radiation.

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)
US445704A 1965-04-05 1965-04-05 Diazo reproduction Expired - Lifetime US3418469A (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
US445704A US3418469A (en) 1965-04-05 1965-04-05 Diazo reproduction
DE19661572076 DE1572076A1 (de) 1965-04-05 1966-04-02 Diazotypieverfahren und Diazotypiematerial
AT320066A AT277752B (de) 1965-04-05 1966-04-04 Diazotypiematerial
SE04502/66A SE326102B (de) 1965-04-05 1966-04-04
BE678993D BE678993A (de) 1965-04-05 1966-04-04
NL6604532A NL6604532A (de) 1965-04-05 1966-04-05
FR56426A FR1473770A (fr) 1965-04-05 1966-04-05 Procédé et matériel pour la diazotypie
GB15108/66A GB1134943A (en) 1965-04-05 1966-04-05 Improvements in and relating to diazo-type reproduction

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US445704A US3418469A (en) 1965-04-05 1965-04-05 Diazo reproduction

Publications (1)

Publication Number Publication Date
US3418469A true US3418469A (en) 1968-12-24

Family

ID=23769896

Family Applications (1)

Application Number Title Priority Date Filing Date
US445704A Expired - Lifetime US3418469A (en) 1965-04-05 1965-04-05 Diazo reproduction

Country Status (7)

Country Link
US (1) US3418469A (de)
AT (1) AT277752B (de)
BE (1) BE678993A (de)
DE (1) DE1572076A1 (de)
GB (1) GB1134943A (de)
NL (1) NL6604532A (de)
SE (1) SE326102B (de)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3514597A (en) * 1966-04-05 1970-05-26 Agfa Gevaert Nv Thermographic recording processes and materials
US4650738A (en) * 1984-10-22 1987-03-17 American Hoechst Corporation Negative working diazo color proofing method
US4659642A (en) * 1984-10-22 1987-04-21 American Hoechst Corporation Positive working naphthoquinone diazide color proofing transfer process
US5124227A (en) * 1990-03-15 1992-06-23 Graphics Technology International Inc. Protective overcoats for diazo type layers

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2597306A (en) * 1949-10-05 1952-05-20 Little Inc A Printing process wherein an alkaline substance passing through stencil openings effects coupling of an azo dye in situ
US2691587A (en) * 1949-07-20 1954-10-12 Rca Corp Developing of diazotype images
US2732299A (en) * 1952-07-22 1956-01-24 Light sensitive
US3027256A (en) * 1957-11-22 1962-03-27 Dietzgen Co Eugene Production of light-sensitive diazotype materials
US3046128A (en) * 1958-07-03 1962-07-24 Dietzgen Co Eugene Thermally developable diazotype photoprinting material and production thereof
FR1336307A (fr) * 1962-07-19 1963-08-30 Bauchet & Cie Ets Produit diazotype photosensible développable par la chaleur et son procédé de préparation
FR1377477A (fr) * 1963-09-24 1964-11-06 Bauchet & Cie Ets Procédé de fabrication d'un article à surface photosensible diazotype thermodéveloppable et article réalisé par application de ce procédé
US3272629A (en) * 1962-01-25 1966-09-13 Nashua Corp Photosensitive diazotype materials
US3284201A (en) * 1961-12-21 1966-11-08 Grinten Chem L V D Three layered light-sensitive diazotype material

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2691587A (en) * 1949-07-20 1954-10-12 Rca Corp Developing of diazotype images
US2597306A (en) * 1949-10-05 1952-05-20 Little Inc A Printing process wherein an alkaline substance passing through stencil openings effects coupling of an azo dye in situ
US2732299A (en) * 1952-07-22 1956-01-24 Light sensitive
US3027256A (en) * 1957-11-22 1962-03-27 Dietzgen Co Eugene Production of light-sensitive diazotype materials
US3046128A (en) * 1958-07-03 1962-07-24 Dietzgen Co Eugene Thermally developable diazotype photoprinting material and production thereof
US3284201A (en) * 1961-12-21 1966-11-08 Grinten Chem L V D Three layered light-sensitive diazotype material
US3272629A (en) * 1962-01-25 1966-09-13 Nashua Corp Photosensitive diazotype materials
FR1336307A (fr) * 1962-07-19 1963-08-30 Bauchet & Cie Ets Produit diazotype photosensible développable par la chaleur et son procédé de préparation
FR1377477A (fr) * 1963-09-24 1964-11-06 Bauchet & Cie Ets Procédé de fabrication d'un article à surface photosensible diazotype thermodéveloppable et article réalisé par application de ce procédé

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3514597A (en) * 1966-04-05 1970-05-26 Agfa Gevaert Nv Thermographic recording processes and materials
US4650738A (en) * 1984-10-22 1987-03-17 American Hoechst Corporation Negative working diazo color proofing method
US4659642A (en) * 1984-10-22 1987-04-21 American Hoechst Corporation Positive working naphthoquinone diazide color proofing transfer process
US5124227A (en) * 1990-03-15 1992-06-23 Graphics Technology International Inc. Protective overcoats for diazo type layers

Also Published As

Publication number Publication date
GB1134943A (en) 1968-11-27
BE678993A (de) 1966-09-16
DE1572076A1 (de) 1970-02-12
AT277752B (de) 1970-01-12
SE326102B (de) 1970-07-13
NL6604532A (de) 1966-10-06

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AS Assignment

Owner name: SECURITY NATIONAL BANK, A NATIONAL BANKING ASSOCIA

Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808

Effective date: 19820323

Owner name: CHASE MANHATTAN BANK, N.A. THE; A NATIONAL BANKING

Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808

Effective date: 19820323

Owner name: CHEMICAL BANK, A BANKING INSTITUTION OF NY.

Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808

Effective date: 19820323

Owner name: CONTINENTAL ILLINOIS NATIONAL BANK & TRUST CO., OF

Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808

Effective date: 19820323

Owner name: BANK OF CALIFORNIA N.A. THE; A NATIONAL BANKING AS

Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808

Effective date: 19820323

Owner name: CHEMICAL BANK, A BANKING INSTITUTION OF, NEW YORK

Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808

Effective date: 19820323