DE534637C - Process for dyeing and printing cellulose esters and ethers - Google Patents

Process for dyeing and printing cellulose esters and ethers

Info

Publication number
DE534637C
DE534637C DEI39118D DEI0039118D DE534637C DE 534637 C DE534637 C DE 534637C DE I39118 D DEI39118 D DE I39118D DE I0039118 D DEI0039118 D DE I0039118D DE 534637 C DE534637 C DE 534637C
Authority
DE
Germany
Prior art keywords
ethers
dyeing
cellulose esters
printing cellulose
phenol
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
DEI39118D
Other languages
German (de)
Inventor
Dr Hans Kaemmerer
Dr Emil Weber
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 DEI39118D priority Critical patent/DE534637C/en
Application granted granted Critical
Publication of DE534637C publication Critical patent/DE534637C/en
Expired legal-status Critical Current

Links

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
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/10Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
    • C09B29/12Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group of the benzene series
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/34Material containing ester groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Coloring (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Description

Verfahren zum Färben und Bedrucken von Celluloseestern und -äthern Es wurde gefunden, daß man Cellulos.eester und -äther in vorzüglicher Weise färben und bedrucken kann, wenn man hierbei Monoazofarbstoffe, die durch Kuppeln von diazotierten aromatischen Verbindungen mit Phenol oder Phenolderivaten, deren Parastellung zur Hydroxylgruppe unbesetzt ist und die außer Alkylgruppen keine weiteren Substituenten enthalten, erhalten werden, verwendet. Die erhaltenen Färbungen zeichnen sich durch hervorragende Lichtechtheit und sonstige sehr gute Echtheitseigenschaften aus. Außerdem haben die Färbungen den Vorteil, daß sie nicht phototrop sind.Process for dyeing and printing cellulose esters and ethers It has been found that cellulose esters and ethers can be dyed in an excellent manner and can be printed if one uses monoazo dyes that are diazotized by coupling aromatic compounds with phenol or phenol derivatives, their para position to Hydroxyl group is unoccupied and apart from alkyl groups no further substituents contain, are obtained, used. The colorations obtained are distinguished excellent lightfastness and other very good fastness properties. aside from that the colorations have the advantage that they are not phototropic.

Die Eigenschaften der verwendeten Farbstoffe können noch verbessert werden, wenn man sie mit Halogenallkylen, Säurechloriden usw. nachbehandelt.The properties of the dyes used can still be improved if they are aftertreated with halogen alkyls, acid chlorides, etc.

Beispiel i Acetatseide wird in der üblichen Weise mit dem durch Kuppeln von diazotiertem Monoacetyl-p-phenylendiamin mit o-Kresol erhaltenen Farbstoff i Stunde lang bei 6o bis 8o° gefärbt. Man erhält eine gelbe, nicht phototrope Färbung von hervorragender Lichtechtheit. Ähnliche Färbungen erhält man mit anderen Monoazofarbstoffen, die sich von anderen Phenolen mit freier Parastellung, z. B. m-Kresol usw., ableiten. Beispiel z Man färbt Acetatseide in der üblic'he;n Weise mit dem mit Chloräthyl behandelten Farbstoff aus diazotiertem Anilin und Phenol. Man erhält eine gelbe Färbung von ausgezeichneten Echtheitseigenschaften.Example i Acetate silk is made in the usual manner with the coupling dye obtained from diazotized monoacetyl-p-phenylenediamine with o-cresol i Stained at 6o to 8o ° for 1 hour. A yellow, non-photochromic coloration is obtained of excellent lightfastness. Similar colorations are obtained with other monoazo dyes, which differ from other phenols with a free para position, e.g. B. m-cresol, etc., derive. Example z Acetate silk is dyed in the usual way with that of chloroethyl treated diazotized aniline and phenol dye. A yellow one is obtained Coloring with excellent fastness properties.

Claims (1)

PATE NTANSPRUCÜ: Verfahren zum Färben und Bedrucken von Celluloseestern und -äthern, dadurch gekennzeichnet, daß, man Monoazofarbstoffe, die durch Kuppeln von diazotierten aromatischen Verbindungen -mit Phenol oder Phenolderivaten, deren Parastellung zur Hydroxylgruppe unbesetzt ist und die außer Allkylgruppen keine weiteren Substituenten enthalten, erhalten werden und die gegebenenfalls noch einer Nachbehandlung mit Halogenalkylen, Säurechloriden u. dgl. unterworfen sein können, verwendet. PATE NTANSPRUCÜ: Process for dyeing and printing cellulose esters and ethers, characterized in that monoazo dyes obtained by coupling diazotized aromatic compounds with phenol or phenol derivatives whose para position to the hydroxyl group is unoccupied and which apart from alkyl groups contain no further substituents, are obtained and which can optionally also be subjected to an aftertreatment with haloalkylenes, acid chlorides and the like.
DEI39118D 1929-08-27 1929-08-27 Process for dyeing and printing cellulose esters and ethers Expired DE534637C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEI39118D DE534637C (en) 1929-08-27 1929-08-27 Process for dyeing and printing cellulose esters and ethers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI39118D DE534637C (en) 1929-08-27 1929-08-27 Process for dyeing and printing cellulose esters and ethers

Publications (1)

Publication Number Publication Date
DE534637C true DE534637C (en) 1931-09-30

Family

ID=7189976

Family Applications (1)

Application Number Title Priority Date Filing Date
DEI39118D Expired DE534637C (en) 1929-08-27 1929-08-27 Process for dyeing and printing cellulose esters and ethers

Country Status (1)

Country Link
DE (1) DE534637C (en)

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