CH127534A - Colored varnish and process for its manufacture. - Google Patents

Colored varnish and process for its manufacture.

Info

Publication number
CH127534A
CH127534A CH127534DA CH127534A CH 127534 A CH127534 A CH 127534A CH 127534D A CH127534D A CH 127534DA CH 127534 A CH127534 A CH 127534A
Authority
CH
Switzerland
Prior art keywords
manufacture
colored
unsulfated
colored varnish
general formula
Prior art date
Application number
Other languages
German (de)
Inventor
Gesellschaft Fuer Chemis Basel
Original Assignee
Chem Ind Basel
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 Chem Ind Basel filed Critical Chem Ind Basel
Publication of CH127534A publication Critical patent/CH127534A/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B67/00Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0071Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
    • C09B67/008Preparations of disperse dyes or solvent dyes
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B39/00Other azo dyes prepared by diazotising and coupling
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D101/00Coating compositions based on cellulose, modified cellulose, or cellulose derivatives
    • C09D101/08Cellulose derivatives
    • C09D101/16Esters of inorganic acids
    • C09D101/18Cellulose nitrate

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)

Description

  

  Gefärbter Lack und     Verfahren    zu dessen Herstellung.    Es ist bekannt, dass zur Herstellung von  lichtecht gefärbten Lacken (welche auf Zel  lulose- oder     Phenolaldehydbasis    hergestellt  sein können),     Aminoanthrachinone    verwendet  werden     können.     



  Es wurde nun die wichtige Beobachtung  gemacht, dass man ausserordentlich lichtechte  gelbe bis blaurot gefärbte Lacke herstellen  kann, .wenn man Lacke mit solchen Farb  stoffen färbt, welche der allgemeinen Formel       R,-N=N-R..    entsprechen, in welcher     R1     den aromatischen Kern einer negativ substi  tuierten,     unsulfierten        Diazoverbindung    und       R2    ein beliebiges, in der     4-.Stellung    zur     Amino-          gruppe    kuppelndes aromatisches Amin be  deutet.  



  <I>Beispiel</I>     .1:     Man löst 4 bis 5 Teile des durch Ver  einigen 'von     diazotiertem        p-Nitranilin    und       Kresidin    erhältlichen Farbstoffes in 1000  Teilen fertigem     Zaponlack.    Die so erhaltene  Flüssigkeit, in dünner Schicht auf die ver  schiedensten Unterlagen (Metall, Glas, Leder,  Holz, Zelluloid, Seide usw.) aufgebracht,    hinterlässt beim Eintrocknen einen transpa  renten Überzug, dessen intensiv scharlach  rote Farbe vorzüglich lichtecht ist. Durch  Einverleibung geeigneter Zusätze kann der  transparente Lack in einen Matt- oder Deck  lack übergeführt werden.  



  <I>Beispiel 2:</I>  Man versetzt, gegebenenfalls unter Zu  gabe weiterer Lösungsmittel und der üblichen       Weichmachungs-        bezw.        Plastifizierungs-          mittel,    eine     Nitrozelluloselösung    mit einer     ace-          tonischen.    Lösung von     4-Nitro-4'-aminoazo-          benzol.    Der so erhaltene Lack wird zur Her  stellung von orangeroten Überzügen von vor  züglicher Lichtechtheit verwendet.  



  Ähnliche Resultate erhält man mit Lacken  aus     Acetylzellulose    oder aus     Phenol-Alde-          hydkondensationsprodukten.    Im letzteren  Fall widerstehen die Färbungen den verschie  denen     H;ärtungsverfahren.     



  Gelbe Lacke erhält man mit Produkten  wie     2.5-Dichlor-4'-aminoazobenzol        bezw.        2.5-          Dichlor-4'-amino-3'-methylazobenzol,    orange  farbene mit     3-Nitro-4'-aminoazobenzol,    schar-      lachrote mit     4-Nitro-4'-amino-2'-acetylamino-          azobenzol,    blaurote mit     4-Nitro-2-methoxy-4'-          dialkylaminoazobenzol    usw.

   Gut geeignet sind  ebenfalls die     Azofarbstoffe    aus     unsulfierten     negativ substituierten     Diazoverbindungen    und       Diphenylaminen,    ferner aus     Benzyl-        bezw.          Äthylbenzyl-        bezw.        Dibenzylanilin.  



  Colored varnish and process for its manufacture. It is known that for the production of lightfast colored paints (which can be made on a cellulose or phenolaldehyde basis), aminoanthraquinones can be used.



  The important observation has now been made that extremely lightfast yellow to blue-red colored paints can be produced, if paints are colored with those dyes which correspond to the general formula R, -N = NR .., in which R1 is the aromatic nucleus a negatively substituted, unsulfated diazo compound and R2 is any aromatic amine coupling in the 4-position to the amino group.



  <I> Example </I> .1: 4 to 5 parts of the dye obtainable by combining diazotized p-nitroaniline and cresidine are dissolved in 1000 parts of finished zapon varnish. The liquid obtained in this way, applied in a thin layer to a wide variety of substrates (metal, glass, leather, wood, celluloid, silk, etc.), leaves a transparent coating when it dries, the intense scarlet red color of which is extremely lightfast. By incorporating suitable additives, the transparent lacquer can be converted into a matt or top lacquer.



  <I> Example 2 </I> The mixture is added, optionally with the addition of further solvents and the usual plasticizing or Plasticizer, a nitrocellulose solution with an acetic one. Solution of 4-nitro-4'-aminoazobenzene. The varnish obtained in this way is used for the manufacture of orange-red coatings of excellent lightfastness.



  Similar results are obtained with lacquers made from acetyl cellulose or from phenol-aldehyde condensation products. In the latter case, the colorations resist the various hardening processes.



  Yellow lacquers are obtained with products such as 2.5-dichloro-4'-aminoazobenzene or. 2.5- dichloro-4'-amino-3'-methylazobenzene, orange colored with 3-nitro-4'-aminoazobenzene, sharp red with 4-nitro-4'-amino-2'-acetylamino-azobenzene, blue-red with 4- Nitro-2-methoxy-4'-dialkylaminoazobenzene etc.

   The azo dyes from unsulfated negatively substituted diazo compounds and diphenylamines, and also from benzyl or benzyl, are also suitable. Ethylbenzyl- respectively. Dibenzylaniline.

 

Claims (1)

PATENTANSPRÜCHE: I. Gefärbter lichtechter Lack, dadurch ge kennzeichnet, dass er einen solchen Farb stoff enthält, der der allgemeinen Formel R,-N=N-R2 entspricht, in welcher R, den aromatischen Kern einer negativ sub stituierten; unsulfierten Diazoverbin- dung, und R2 ein beliebiges, in der 4- Stellung zur Aminogruppe kuppelndes, aromatisches Amin bedeutet. Il. Verfahren zur Herstellung eines ge färbten lichtechten Lackes nach Patent anspruch I, dadurch gekennzeichnet, dass man einen. PATENT CLAIMS: I. Dyed, lightfast paint, characterized in that it contains such a dye which corresponds to the general formula R, -N = N-R2, in which R, the aromatic nucleus of a negatively substituted one; unsulfated diazo compound, and R2 is any aromatic amine which couples in the 4 position to the amino group. Il. Process for the production of a colored lightfast paint according to claim I, characterized in that one. Lack mit einem Farbstoff der allgemeinen Formel R,-N=N-R2, in welcher R, den aromatischen Kern einer negativ substituierten, unsulfierten Di- azoverbindung, und R_# ein beliebiges, in der 4-Stellung zur Aminogruppe kup- pelndes aromatisches Amin bedeutet, färbt. Lacquer with a dye of the general formula R, -N = N-R2, in which R, the aromatic nucleus of a negatively substituted, unsulfated diazo compound, and R_ # any aromatic amine coupling in the 4-position to the amino group means, colors.
CH127534D 1927-02-10 1927-02-10 Colored varnish and process for its manufacture. CH127534A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH127534T 1927-02-10

Publications (1)

Publication Number Publication Date
CH127534A true CH127534A (en) 1928-09-01

Family

ID=4386074

Family Applications (1)

Application Number Title Priority Date Filing Date
CH127534D CH127534A (en) 1927-02-10 1927-02-10 Colored varnish and process for its manufacture.

Country Status (1)

Country Link
CH (1) CH127534A (en)

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