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AT135053B - Process for preserving diazo solutions. - Google Patents

Process for preserving diazo solutions.

Info

Publication number
AT135053B
AT135053B AT135053DA AT135053B AT 135053 B AT135053 B AT 135053B AT 135053D A AT135053D A AT 135053DA AT 135053 B AT135053 B AT 135053B
Authority
AT
Austria
Prior art keywords
preserving
solutions
diazo
diazo solutions
desc
Prior art date
Application number
Other languages
German (de)
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
Application granted granted Critical
Publication of AT135053B publication Critical patent/AT135053B/en

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
    • 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
    • C09B67/0079Azoic dyestuff preparations

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

   <Desc/Clms Page number 1> 
 



  Verfahren zum Haltbarmaehen von Diazolösungen. 



   Es ist bekannt, dass in Diazolösungen, wie man sie zur Herstellung von Azofarbstoffen auf der Faser verwendet, je nach der Haltbarkeit der Diazoverbindung nach kürzerem oder längerem Stehen sich Ausscheidungen von Zersetzungsprodukten bilden, welche die Reibechtheit der Färbung, insbesondere bei Apparatfärbungen, sehr ungünstig beeinflussen. 



   Es wurde nun gefunden, dass das Auftreten dieser Ausscheidungen praktisch dadurch verhindert werden kann, dass man den Diazolösungen Dispergier-oder Emulgiermittel, die bei saurer Reaktion beständige Lösungen bilden, zusetzt. Als Dispergier-bzw. Emulgiermittel seien beispielsweise genannt : gereinigte Sulfitablauge, die Umsetzungsprodukte von Carbonsäuren aliphatischer, cycloaliphatischer oder aromatisch-aliphatischer Natur mit organischen Aminosulfonsäuren, deren Herstellung den Gegenstand der englischen Patente Nr. 341053,343524 und 343899 bildet ; ferner Verbindungen, die man dadurch erhält, dass man in organische Verbindungen, die eine oder mehrere Oxy-,   Carboxy-oder   Aminogruppen enthalten,   Polyglylcolätherreste   mit 4 oder mehr Äthylengruppen einführt (vgl. franz. 



  Patent Nr. 727202) oder auch esterartige Kondensationsprodukte, wie sie nach dem Verfahren des franz. Patentes Nr. 705801 erhalten werden können. 



   Die Menge des zuzusetzenden Dispergier-oder Emulgiermittels kann in weiten Grenzen schwanken, jedoch genügen im allgemeinen 1-3   g   auf   l .   Die Lösungen bleiben dadurch während der ganzen Dauer ihres Gebrauches klar und zeigen eine sehr gute Haltbarkeit. 



   Beispiel : 2 g   4-Chlor-l-methyl-2-aminobenzol   werden in der   üblichen   Weise diazotiert, mit essigsaurem Natrium abgestumpft und nach dem Auffüllen auf   l   mit 1 g Oleylmethyltaurin (hergestellt nach Beispiel 4 des engl. Patentes Nr. 343899) versetzt. Mit dieser Lösung wird Baumwolle, welche mit   2-oxynaphthalin-3-carbonsänre-o-toluidid   imprägniert ist, in der üblichen Weise entwickelt. 



   Die in derselben Weise hergestellte Diazolösung zeigt ohne den Zusatz von Oleylmethyltaurin schon nach kurzer Zeit (etwa   %-1   Stunde) rosa gefärbte, flockige Ausscheidungen. 



   An Stelle des Oleylmethyltaurin kann mit demselben Erfolg z. B. auch Oleylhydroxyäthannatriumsulfonat verwendet werden (siehe z. B. franz. Patent Nr.   705 081)   oder Produkte, die durch Einwirkung von 20 Mol Äthylenoxyd auf 1 Mol   Octodecylalkohol   oder 1 Mol von Oleylalkohol (siel. e z. B. franz. Patent Nr. 727702) erhalten werden. 

**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.



   <Desc / Clms Page number 1>
 



  Process for the preservation of diazo solutions.



   It is known that in diazo solutions, such as those used for the production of azo dyes on the fiber, depending on the durability of the diazo compound, after a shorter or longer period of standing, decomposition products form, which have a very unfavorable effect on the rubbing fastness of the dyeing, especially in the case of machine dyeing .



   It has now been found that the occurrence of these precipitates can practically be prevented by adding dispersants or emulsifiers, which form stable solutions in the event of an acid reaction, to the diazo solutions. As a dispersing or. Examples of emulsifiers are: purified sulphite waste liquor, the reaction products of carboxylic acids of aliphatic, cycloaliphatic or aromatic-aliphatic nature with organic aminosulphonic acids, the production of which is the subject of English patents 341053,343524 and 343899; Furthermore, compounds obtained by introducing polyglylcolether radicals with 4 or more ethylene groups into organic compounds which contain one or more oxy, carboxy or amino groups (cf.



  Patent No. 727202) or ester-like condensation products, as they are according to the method of the French. Patent No. 705801 can be obtained.



   The amount of dispersant or emulsifier to be added can vary within wide limits, but 1-3 g per liter are generally sufficient. The solutions thus remain clear for the entire duration of their use and have a very good shelf life.



   Example: 2 g of 4-chloro-1-methyl-2-aminobenzene are diazotized in the usual way, blunted with acetic acid sodium and, after making up to 1, mixed with 1 g of oleylmethyltaurine (prepared according to Example 4 of English Patent No. 343899) . Cotton impregnated with 2-oxynaphthalene-3-carboxylic acid o-toluidide is developed with this solution in the usual way.



   The diazo solution prepared in the same way shows, without the addition of oleylmethyltaurine, pink-colored, flaky precipitates after a short time (approx.



   Instead of oleylmethyltaurine, z. B. Oleylhydroxyäthannatriumsulfonat can be used (see z. B. French. Patent No. 705 081) or products that by the action of 20 moles of ethylene oxide on 1 mole of octodecyl alcohol or 1 mole of oleyl alcohol (siel. E. B. French. Patent No. 727702).

** WARNING ** End of DESC field may overlap beginning of CLMS **.

 

Claims (1)

PATENT-ANSPRUCH : Verfahren zum Haltbarmachen von Diazolösungen, dadurch gekennzeichnet, dass man denselben Dispergier-oder Emulgiermittel, die bei saurer Reaktion beständige Lösungen bilden, zusetzt. **WARNUNG** Ende CLMS Feld Kannt Anfang DESC uberlappen**. PATENT CLAIM: Process for preserving diazo solutions, characterized in that the same dispersing or emulsifying agents which form stable solutions in the event of an acid reaction are added. ** WARNING ** End of CLMS field may overlap beginning of DESC **.
AT135053D 1931-10-05 1932-09-24 Process for preserving diazo solutions. AT135053B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI42736D DE593790C (en) 1931-10-05 1931-10-05 Process for preserving diazo solutions

Publications (1)

Publication Number Publication Date
AT135053B true AT135053B (en) 1933-10-25

Family

ID=7190852

Family Applications (1)

Application Number Title Priority Date Filing Date
AT135053D AT135053B (en) 1931-10-05 1932-09-24 Process for preserving diazo solutions.

Country Status (5)

Country Link
AT (1) AT135053B (en)
CH (1) CH162738A (en)
DE (1) DE593790C (en)
FR (1) FR743545A (en)
NL (1) NL35402C (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE468202A (en) * 1945-07-04

Also Published As

Publication number Publication date
DE593790C (en) 1934-03-06
FR743545A (en)
NL35402C (en)
CH162738A (en) 1933-07-15

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