DE458825C - Process for making blueprints and photocopies - Google Patents

Process for making blueprints and photocopies

Info

Publication number
DE458825C
DE458825C DEI30470D DEI0030470D DE458825C DE 458825 C DE458825 C DE 458825C DE I30470 D DEI30470 D DE I30470D DE I0030470 D DEI0030470 D DE I0030470D DE 458825 C DE458825 C DE 458825C
Authority
DE
Germany
Prior art keywords
photocopies
blueprints
sulfonic acid
developed
naphthoquinone
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
Application number
DEI30470D
Other languages
German (de)
Inventor
Dr Max Raeck
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to DEI30470D priority Critical patent/DE458825C/en
Application granted granted Critical
Publication of DE458825C publication Critical patent/DE458825C/en
Expired 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
    • G03C1/72Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705
    • G03C1/73Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705 containing organic compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Verfahren zur Herstellung von Lichtpausen und Photokopien. Es ist bekannt, daß i, 2-naphthochinon-4-sulfosaure Salze mit organischen Verbindungen, «-elche eine oder mehrere freie Aminogruppen enthalten, unter Abspaltung der Sulfogruppe sehr leicht farbige Chinonanile bilden.Process for making blueprints and photocopies. It is known that i, 2-naphthoquinone-4-sulfonic acid salts with organic compounds, «-Which contain one or more free amino groups, with elimination of the sulfo group very easily form colored quinone aniles.

Wie gefunden wurde, sind i, 2-naplithocliinon-4-sulfosaure Salze sehr lichtempfindlich, so daß sich der genannte Vorgang mit Vorteil zur Herstellung von gefärbten Photokopien, Lichtpausen u. dgl. verwenden läßt. Man macht Papier oder mit einer Gelatineschicht überzogenes Papier, Glas oder Film durch Behandeln mit Lösungen von i, 2-naplitliochinon-4-sulfosauren Salzen lichtempfindlich, belichtet, z. B. unter einer Zeichnung auf Pauspapier, und entwickelt mit organischen Verbindungen, welche eine oder mehrere i Aminogruppen enthalten, wobei unmittelbar ein positives Bild der Zeichnung entsteht.As has been found, 1,2-naplithocliinone-4-sulfonic acid salts are very photosensitive, so that said process is advantageous for the production of colored photocopies, blueprints and the like. One makes paper or paper, glass or film coated with a gelatin layer by treating with Solutions of i, 2-naplitlioquinone-4-sulfonic acid salts light-sensitive, exposed, z. B. under a drawing on tracing paper, and developed with organic compounds, which contain one or more amino groups, with a positive immediately Image of the drawing is created.

Beispiel i.Example i.

Ein mit einer zweiprozentigen Lösung von i, 2-naphthocliinoti-4-sulfosaurem Kalium getränktes und getrocknetes Papier wird unter einem Schwarz-Weiß-Positit- belichtet und danach in einer einprozentigen Lösung von salzsaurem Anilin entwickelt. Die vor der Belichtung geschützten Stellen erscheinen rot auf farblosem Grunde.One with a two percent solution of i, 2-naphthocliinoti-4-sulfonic acid Potassium soaked and dried paper is displayed under a black and white position exposed and then developed in a one percent solution of hydrochloric aniline. The areas protected from exposure appear red on a colorless background.

Beispiel e.Example e.

Papier wird begossen mit einer Gelatinelösung, welche i, 2-naphthochinon-4-sulfosaures Kali enthält. Nach dem Trocknen und Belichten wird mit einer einprozentigen wäßrigen Lösung von i-Methyl-2, 4-diaminobenzol entwickelt. Man erhält bordeauxrote Töne.Paper is doused with a gelatin solution containing 1,2-naphthoquinone-4-sulfosaures Contains potash. After drying and exposure, a one percent aqueous solution is used Solution of i-methyl-2, 4-diaminobenzene developed. Bordeaux-red tones are obtained.

Beispiel 3. Example 3.

Eine i, 2-naphthochinon-4-sulfosaures Kali enthaltende Gelatinelösung wird auf Glas gegossen. Nach dem Trocknen und Belichten wird mit einer Lösung von i-Amino-4-oxybenzol entwickelt. Man erhält violette Töne.A gelatin solution containing 1,2-naphthoquinone-4-sulphonic acid potassium is poured onto glass. After drying and exposure, a solution of i-Amino-4-oxybenzene developed. Purple tones are obtained.

Claims (1)

PA TENTANSPRUCII Verfahren zur Herstellung von Lichtpausen und Photokopien, dadurch gekennzeichnet, daß man als lichtempfindlichen Stoff i, 2-naphthochinon-4-sulfosaureSalzeverwendet und nach erfolgter Belichtung das Bild mit organischen, freie Aminogruppen enthaltenden Verbindungen entwickelt.PA TENTANSPRUCII Process for the production of blueprints and photocopies, characterized in that i, 2-naphthoquinone-4-sulfonic acid salts are used as the photosensitive substance and after exposure, the image with organic free amino groups containing Connections developed.
DEI30470D 1927-02-28 1927-03-01 Process for making blueprints and photocopies Expired DE458825C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEI30470D DE458825C (en) 1927-02-28 1927-03-01 Process for making blueprints and photocopies

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEI0030470 1927-02-28
DEI30470D DE458825C (en) 1927-02-28 1927-03-01 Process for making blueprints and photocopies

Publications (1)

Publication Number Publication Date
DE458825C true DE458825C (en) 1928-04-18

Family

ID=25981405

Family Applications (1)

Application Number Title Priority Date Filing Date
DEI30470D Expired DE458825C (en) 1927-02-28 1927-03-01 Process for making blueprints and photocopies

Country Status (1)

Country Link
DE (1) DE458825C (en)

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