DE727917C - Process for improving the fastness properties of dyeings with substantive dyes on cellulose fibers - Google Patents
Process for improving the fastness properties of dyeings with substantive dyes on cellulose fibersInfo
- Publication number
- DE727917C DE727917C DEI48174D DEI0048174D DE727917C DE 727917 C DE727917 C DE 727917C DE I48174 D DEI48174 D DE I48174D DE I0048174 D DEI0048174 D DE I0048174D DE 727917 C DE727917 C DE 727917C
- Authority
- DE
- Germany
- Prior art keywords
- dyeings
- cellulose fibers
- improving
- substantive dyes
- fastness properties
- 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
Links
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General 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
- D06P1/44—General 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 insoluble pigments or auxiliary substances, e.g. binders
- D06P1/655—Compounds containing ammonium groups
- D06P1/66—Compounds containing ammonium groups containing quaternary ammonium groups
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Paper (AREA)
- Coloring (AREA)
Description
Verfahren zur Verbesserung der Echtheitseigenschaften von Färbungen mit substantiven Farbstoffen auf Cellulosefasern Es wurde gefunden, daß man die Echtheitseigenschaften von Färbungen mit substantiven Farbstoffen auf Cellulosefasern verbessern kann, wenn man die gefärbte Faser mit Lösungen von Salzen quartärer Ammoniumbasen nachbehandelt, die durch energische Peralkylierung von Basengemischen hergestellt sind, welc2ie im wesentlichen Polyalkylenpolyamine der allgemeinen Formel H2N-(AlkylenNH) > 2alkylenNH2 enthalten.Process for improving the fastness properties of dyeings with substantive dyes on cellulose fibers It has been found that the Fastness properties of dyeings with substantive dyes on cellulose fibers can improve if the dyed fiber with solutions of salts of quaternary ammonium bases post-treated, which is produced by vigorous peralkylation of base mixtures are, which are essentially polyalkylenepolyamines of the general formula H2N- (AlkylenNH) > 2alkyleneNH2 included.
lm Vergleich mit den bisher aus dem Schriftdun bekannten Verfahren zur Nachbehandlung von Färbungen auf Cellulosefasern mit Lösungen von quartären Ammoniumverbindungen (vgl. die brifischen Patentschriften 3669I8, 383 634 und 39o 553 sowie die französische Patentschrift 748 5I6) zeigt sich das vorliegende Verfahren, namentlich in bezug auf die Waschechtheit, bei weitem überlegen.In comparison with the methods known so far from the document in Dun for the aftertreatment of dyeings on cellulose fibers with solutions of quaternary Ammonium compounds (see British patents 3669I8, 383 634 and 39o 553 as well as the French patent 748 5I6) shows the present process, especially in terms of fastness to washing, far superior.
Von den möglichen Polyaminen ist das Polyäthylendiamin technisch am leichtesten zugänglich. Dieses ist bekanntlich ein Gemischpolymerer Äthylendiamine. von der allgemeinen Formel NH2(C2H4NH)nC2H4NH2,. denen Verbindungen von der allgemeinen Formel (C2H4NH)n (Piperazin und ähnliche Verbindungen) beigemischt sind. Während Athylendiamin selbst und die nächsthöheren Polymeren, beispielsweise Diäthylentriamin, Triäthylentriamin, Triäthylentetramin einer Kondensationsreaktion bedürfen, um nach ihrer Überführung in. Ammoniumbasenbrauchbare Nachbehandlungsmittel für Substantive Färbungen zu ergeben, können Gemischepolymerer Basen, die in der Hauptsache Verbindungen enthalten, bei denen im Sinne der obigen Formeln n < 2 ist, schon durch energische Peralkylierung allein in wertvolle Nachbehandlungsmittel übergeführt werden. Hierbei ist eine möglichst vollständige Alkylierung von Vorteil, bei welcher möglichst viele der vorhandenen Stickstoffatome in den fünfwertigen Zustand übergeführt werden. Beispiel Eine zur Nächbehandlung substantiver Färbangen geeignete qüartäre Ammoniumbase kann z. B. in folgender Weise hergestellt werden: ' Aus einem Gemisch polymerer Äthy@endamne destilliert man bei einem Vakuum: von io mm die bis 22o° C übergehenden Anteile ab, I 5o Teile des Rückstandes,der eine zähe braune Flüssigkeit darstellt,, löst man in 2ooo Teilen Wasser und setzt bei 25 bis 3o° C I2oo Teile Dimethylsulfät allmählich zu und sorgt dabei durch gleichzeitigen Zusatz von Natriumcarbonat für dauernd alkalische Keaktion. Nach beendeter Umsetzung saugt man vom ausgeschiedenen Natriumsulfat ab und erhält eine braune Lösung, die, entsprechend verdünnt, unmittelbar zur Nachbehandlung substantiver Färbungen dienen kann. Die Arbeitsweise ist dabei die gleiche wie im Patent 633 69I.Of the possible polyamines, polyethylene diamine is technically the most Easiest Accessible. This is known to be a mixture of polymeric ethylene diamines. of the general formula NH2 (C2H4NH) nC2H4NH2 ,. which connections from the general Formula (C2H4NH) n (piperazine and similar compounds) are added. While Ethylenediamine itself and the next higher polymers, for example diethylenetriamine, Triethylenetriamine, triethylenetetramine require a condensation reaction in order to their conversion to ammonium bases useful aftertreatment agents for nouns Mixtures of polymeric bases, which are mainly compounds, can be used to produce colorations in which n <2 in the sense of the above formulas, already by energetic Peralkylation alone can be converted into valuable aftertreatment agents. Here As complete an alkylation as possible is advantageous, in which as many as possible of the nitrogen atoms present are converted into the pentavalent state. Example A quaternary ammonium base suitable for subsequent treatment of substantive stains can e.g. B. be prepared in the following way: 'From a mixture of polymeric Ethy @ endamne is distilled in a vacuum: from 10 mm to 22o ° C Shares from, I 50 parts of the residue, which is a viscous brown liquid represents ,, one dissolves in 2,000 parts of water and sets at 25 to 30 ° C I2oo parts Dimethyl sulphate gradually increases and ensures this by the simultaneous addition of sodium carbonate for permanent alkaline reaction. After the reaction has ended, the precipitated product is sucked off Sodium sulfate and receives a brown solution, which, if diluted accordingly, immediately can be used for post-treatment of substantive colorations. The way of working is included the same as in patent 633 69I.
Das als Ausgangskörper dienende Polyamin kann die' verschiedenste Zusammensetzung aufweisen. Ebenso kann die Alkylierung in der verschiedensten Weise, beispielsweise auch mit Arylsulfonsäurealkylestern verschiedener Alkohole oder Benzylchlorid, vorgenommen werden. Die verschiedenen Alkylierungsmittel können auch nacheinander angewendet werden, Man kann auch in bekannter Weise erst mit Alkohol und Salzsäure die tertiäre Base und aus dieser die quartäre Ammoniumbase herstellen.The polyamine used as the starting body can be very diverse Have composition. The alkylation can also be carried out in a wide variety of ways, for example also with arylsulfonic acid alkyl esters of various alcohols or benzyl chloride, be made. The various alkylating agents can also be used one after the other Can also be used in a known manner with alcohol and hydrochloric acid produce the tertiary base and from this the quaternary ammonium base.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEI48174D DE727917C (en) | 1933-10-22 | 1933-10-22 | Process for improving the fastness properties of dyeings with substantive dyes on cellulose fibers |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEI48174D DE727917C (en) | 1933-10-22 | 1933-10-22 | Process for improving the fastness properties of dyeings with substantive dyes on cellulose fibers |
Publications (1)
Publication Number | Publication Date |
---|---|
DE727917C true DE727917C (en) | 1942-11-17 |
Family
ID=7192185
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEI48174D Expired DE727917C (en) | 1933-10-22 | 1933-10-22 | Process for improving the fastness properties of dyeings with substantive dyes on cellulose fibers |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE727917C (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE928713C (en) * | 1952-05-28 | 1955-06-10 | Bayer Ag | Process for the preparation of alkylation products of polyamines |
DE958379C (en) * | 1943-04-09 | 1957-02-21 | Cassella Farbwerke Mainkur Ag | Process for improving the fastness properties of dyeings with substantive dyes on cellulose fibers |
DE1040503B (en) * | 1955-02-23 | 1958-10-09 | Bayer Ag | Post-treatment agent for colorings |
DE1062667B (en) * | 1956-09-07 | 1959-08-06 | Hoechst Ag | Process for improving the fastness properties of dyeings and prints on natural or regenerated cellulose fiber material |
DE1104926B (en) * | 1957-01-19 | 1961-04-20 | Bayer Ag | Process for the aftertreatment of direct dyeing with quaternary polyalkylene polyamines |
DE1224265B (en) * | 1956-10-20 | 1966-09-08 | Bayer Ag | Post-treatment agent for direct dyeing |
DE1492708B1 (en) * | 1963-05-21 | 1972-04-27 | Union Carbide Corp | Packaging sleeves for meat and sausage products |
-
1933
- 1933-10-22 DE DEI48174D patent/DE727917C/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE958379C (en) * | 1943-04-09 | 1957-02-21 | Cassella Farbwerke Mainkur Ag | Process for improving the fastness properties of dyeings with substantive dyes on cellulose fibers |
DE928713C (en) * | 1952-05-28 | 1955-06-10 | Bayer Ag | Process for the preparation of alkylation products of polyamines |
DE1040503B (en) * | 1955-02-23 | 1958-10-09 | Bayer Ag | Post-treatment agent for colorings |
DE1062667B (en) * | 1956-09-07 | 1959-08-06 | Hoechst Ag | Process for improving the fastness properties of dyeings and prints on natural or regenerated cellulose fiber material |
DE1224265B (en) * | 1956-10-20 | 1966-09-08 | Bayer Ag | Post-treatment agent for direct dyeing |
DE1104926B (en) * | 1957-01-19 | 1961-04-20 | Bayer Ag | Process for the aftertreatment of direct dyeing with quaternary polyalkylene polyamines |
DE1492708B1 (en) * | 1963-05-21 | 1972-04-27 | Union Carbide Corp | Packaging sleeves for meat and sausage products |
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