DE263431C - Process for the preservation of diazotized nitroaniline solutions - Google Patents

Process for the preservation of diazotized nitroaniline solutions

Info

Publication number
DE263431C
DE263431C DE1911263431D DE263431DA DE263431C DE 263431 C DE263431 C DE 263431C DE 1911263431 D DE1911263431 D DE 1911263431D DE 263431D A DE263431D A DE 263431DA DE 263431 C DE263431 C DE 263431C
Authority
DE
Germany
Prior art keywords
solutions
preservation
diazotized
sulfonic acids
nitroaniline
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
DE1911263431D
Other languages
German (de)
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.)
Bayer AG
Original Assignee
Farbenfabriken Vorm Friedr Bayer and 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 Farbenfabriken Vorm Friedr Bayer and Co filed Critical Farbenfabriken Vorm Friedr Bayer and Co
Application granted granted Critical
Publication of DE263431C publication Critical patent/DE263431C/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/02General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using azo dyes
    • 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
    • D06P3/58Material containing hydroxyl groups
    • D06P3/60Natural or regenerated cellulose
    • D06P3/68Preparing azo dyes on the material

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Coloring (AREA)

Description

KAISERLICHESIMPERIAL

PATENTAMT.PATENT OFFICE.

PATENTSCHRIFTPATENT LETTERING

KLASSE Sm. GRUPPECLASS Sm. GROUP

Bei Verwendung der diazotierten Nitraniline in der Färberei und Druckerei hat man mit dem Übelstand zu kämpfen, daß die Diazolösungen bzw. die daraus hergestellten Druckfarben schnell unbrauchbar werden.When using the diazotized nitroanilines in dyeing and printing you have with to fight the problem that the diazo solutions or the printing inks produced from them quickly become unusable.

Es wurde nun die Beobachtung gemacht, daß man durch Zusatz von aromatischen Sulfosäuren oder ihren Salzen, wie Naphtalinsulfosäuren oder Anthrachinonsulfosäuren, zuThe observation has now been made that the addition of aromatic Sulfonic acids or their salts, such as naphthalene sulfonic acids or anthraquinone sulfonic acids

ίο den Diazolösungen in einfacher Weise diesem Ubelstand abhelfen kann. Man kann diesen Zusatz vor oder nach dem Diazotieren der Nitraniline vornehmen.ίο the diazo solutions in a simple way this Can help. You can add this before or after the diazotization Make Nitraniline.

Es ist bemerkenswert, daß bereits verhält nismäßig geringe Mengen der Sulfosäuren hierzu ausreichend sind. Verwendet man z. B. eine Naphtalintrisulfosäure, so genügt von dieser Säure bereits 1/i bis x/3 vom Gewicht des angewandten Nitranilins, um eine vorzügliche Haltbarkeit zu erzielen. Aus der Literatur ist es allerdings bekannt, daß man mit Hilfe von Sulfosäuren des Naphtalins haltbare Salze des p-Nitrodiazobenzols in fester Form herstellen kann. Aus dieser Tatsache konnte man aber nicht voraussehen, daß man schon mit weit unter der Theorie liegenden Mengen dieser Sulfosäuren die wässerigen Lösungen der diazotierten Nitraniline haltbar machen kann.It is noteworthy that even relatively small amounts of the sulfonic acids are sufficient for this purpose. If you use z. B. a naphthalene trisulfonic acid, 1 / i to x / 3 of the weight of the nitroaniline used is sufficient to achieve an excellent shelf life. However, it is known from the literature that stable salts of p-nitrodiazobenzene can be prepared in solid form with the aid of sulfonic acids of naphthalene. From this fact, however, one could not foresee that the aqueous solutions of the diazotized nitroanilines could be preserved even with amounts of these sulfonic acids that were far below theoretical.

derthe

Beispiel.Example.

Für Herstellung von Paranitranilinrot wird Stoff mit einer Lösung aus 250 g ß-Naphtol,For the production of Paranitranilinrot, fabric is made with a solution 250 g ß-naphtol,

250 ecm Natronlauge, 360 Be., 3000 ecm Wasser,
500 g Türkischrotöl, 50 prozentig, 100 g Tonerdenatron,
1000 ecm Wasser,
250 ecm caustic soda, 36 0 Be., 3000 ecm water,
500 g Turkish red oil, 50 percent, 100 g clay soda,
1000 ecm of water,

500 g Tragant 65Z500 g tragacanth 65 t

10001000

4040

Auf diese PräparationOn this preparation

4545

1010

geklotzt, getrocknet,
wird gedruckt:
padded, dried,
is printed:

17,7 g Paranitranilinbase werden in 51,6 ecm Salzsäure, 22° Be.,
51,6 ecm kochendem Wasser gelöst. Man fügt 128,9 ccm Eiswasser und
64,5 g Eis zu und rührt langsam 9,9 g Natriumnitrit, in
17.7 g of paranitraniline base are in 51.6 ecm hydrochloric acid, 22 ° Be.,
51.6 ecm of boiling water dissolved. 128.9 cc of ice water are added and
64.5 g of ice and slowly stirred 9.9 g of sodium nitrite, in

64,5 ecm Wasser gelöst, zu. Man läßt 15 Minuten stehen, fügt dann g ι · 3 · 6-Naphtalintrisulfosäure zu, rührt 560,3 g Stärke-Tragant-Verdickung und vor Gebrauch g essigsaures Natron zu.64.5 ecm of water dissolved, too. Leave for 15 minutes stand, then add g · 3 · 6-naphthalene trisulfonic acid, stir Add 560.3 g of starch-tragacanth thickener and sodium acetate before use.

ι kg.ι kg.

!3391 ! 3391

Die Naphtalintrisulfosäure kann ebensogutThe naphthalene trisulfonic acid can as well

nach dem Einrühren der Verdickung oder nach dem Zufügen des essigsauren Natrons zugesetzt werden. Nach dem Drucken wird die Ware getrocknet und gewaschen.after stirring in the thickening or after adding the sodium acetate can be added. After printing, the goods are dried and washed.

Ebenso können andere aromatische Sulfosäuren oder ihre Salze, wie ι · 6-, 1-5-, 2 · 7-, 2 · 6-Naphtalindisulfosäuren, Benzolmono- und -disulfosäuren oder Toluolsulfosäuren oder ihre Salze verwendet werden.Likewise, other aromatic sulfonic acids or their salts, such as ι · 6-, 1-5-, 2 · 7-, 2 · 6-naphthalene disulfonic acids, benzene mono- and disulfonic acids or toluenesulfonic acids or their Salts are used.

Claims (1)

Patent-Anspruch :Patent claim: Verfahren zur Haltbarmachung von diazotierten Nitranilinlösungen, darin bestehend, daß man den Nitranilinen vor oder nach der Diazotierung weniger als die ihnen entsprechenden Mengen von aromatischen Sulfosäuren oder deren Salzen zusetzt.Process for the preservation of diazotized nitroaniline solutions, consisting therein that the nitroanilines before or after the diazotization less than the corresponding amounts of aromatic Adds sulfonic acids or their salts.
DE1911263431D 1911-10-20 1911-10-20 Process for the preservation of diazotized nitroaniline solutions Expired DE263431C (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE263431T 1911-10-20

Publications (1)

Publication Number Publication Date
DE263431C true DE263431C (en) 1913-09-05

Family

ID=32522220

Family Applications (1)

Application Number Title Priority Date Filing Date
DE1911263431D Expired DE263431C (en) 1911-10-20 1911-10-20 Process for the preservation of diazotized nitroaniline solutions

Country Status (3)

Country Link
DE (1) DE263431C (en)
FR (1) FR439535A (en)
GB (1) GB191202037A (en)

Also Published As

Publication number Publication date
FR439535A (en) 1912-06-15
GB191202037A (en) 1912-06-27

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