DE1027630B - Process for the production of textile fabrics ready for use - Google Patents
Process for the production of textile fabrics ready for useInfo
- Publication number
- DE1027630B DE1027630B DEF13880A DEF0013880A DE1027630B DE 1027630 B DE1027630 B DE 1027630B DE F13880 A DEF13880 A DE F13880A DE F0013880 A DEF0013880 A DE F0013880A DE 1027630 B DE1027630 B DE 1027630B
- Authority
- DE
- Germany
- Prior art keywords
- production
- threads
- ready
- textile fabrics
- carbamide resins
- 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.)
- Pending
Links
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/285—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acid amides or imides
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
DEUTSCHESGERMAN
Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung stuhlfertiger Textilgewebe aus natürlichen oder künstlichen Fäden; es besteht darin, daß man dk Fäden mit wäßrigen Lösungen, die polymerisierte Amide ungesättigter niederer Fettsäuren, zur Bildung von Carbamidharzen befähigte Methylolverbindungen und die Bildung der Carbamidharze beschleunigende Katalysatoren enthalten, behandelt, dann bei Temperaturen unterhalb 100° C trocknet und hierauf vor oder nach dem Verweben einer Wärmebehandlung bei Temperaturen über 1000C unterwirft.The present invention relates to a method for the production of textile fabrics ready for use from natural or artificial threads; It consists in treating the threads with aqueous solutions containing polymerized amides of unsaturated lower fatty acids, methylol compounds capable of forming carbamide resins and catalysts which accelerate the formation of carbamide resins, then drying them at temperatures below 100 ° C. and then drying them before or after Interweaving subjected to a heat treatment at temperatures above 100 ° C.
Als polymerisierte Amide ungesättigter niederer Fettsäuren kommen vor allem die Polymerisationsprodukte von Acrylsäureamid und Methacrylsäureamid in Betracht. Unter den zur Bildung von Carbamidharzen befähigten Methylolverbindungen sind Umsetzungsprodukte von Formaldehyd oder Formaldehyd abgebenden Verbindungen, wie Paraformaldehyd, mit Harnstoff, Thioharnstoff, Melamin, Guanidin, Dicyandiamid oder ähnlichen Verbindungen, zu verstehen. Als Katalysatoren, die die Bildung der Carbamidharze zu beschleunigen vermögen, seien Ammoniumsalze starker Säuren, wie z. B. Ammoniumsulfat und Ammoniumnitrat, sowie freie organische Säuren, wie z. B. Milchsäure und Glykolsäure, genannt. Polymerization products are the main polymerized amides of unsaturated lower fatty acids of acrylic acid amide and methacrylic acid amide into consideration. Among those used to form carbamide resins Capable methylol compounds are reaction products of formaldehyde or formaldehyde releasing compounds, such as paraformaldehyde, with urea, thiourea, melamine, Guanidine, dicyandiamide or similar compounds. As catalysts that promote the formation of the Carbamide resins are able to accelerate, ammonium salts of strong acids, such as. B. ammonium sulfate and ammonium nitrate, and free organic acids, such as. B. lactic acid and glycolic acid called.
Geeignete Mengenverhältnisse lassen sich durch Vorversuche leicht ermitteln; von den polymerisierten Amiden und von den Methylolverbindungen verwendet man im allgemeinen gleiche Gewichtsteile, von den Katalysatoren geringere Mengen.Suitable proportions can easily be determined by preliminary tests; from the polymerized Amides and methylol compounds are generally used in equal parts by weight, of the catalysts in smaller amounts.
Die Behandlung der Fäden mit den wäßrigen Lösungen, die die angegebenen Komponenten enthalten, erfolgt in an sich bekannter Weise; das gleiche gilt für das Trocknen der Fäden bei Temperaturen unterhalb 100° C und für die Wärmebehandlung der Fäden oder der hieraus hergestellten Gewebe bei Temperaturen über 100° C.The threads are treated with the aqueous solutions containing the specified components in a manner known per se; the same applies to drying the threads at temperatures below 100 ° C and for the heat treatment of the threads or the fabrics made from them at temperatures over 100 ° C.
Vorzugsweise führt man die Behandlung auf Kettschlichtemaschinen mit Zylindertrocknung durch, da hier die zur Bildung der Carbamidharze notwendige hohe Temperatur bereits während des Schlichtens in ein und demselben Arbeitsgang erreicht wird, so daß sich eine Nachkondensation der aus der geschlichteten Kette gewebten Ware erübrigt.The treatment is preferably carried out on warp sizing machines with cylinder drying, since here the high temperature necessary for the formation of the carbamide resins already during the sizing in one and the same operation is achieved, so that there is a post-condensation of the settled Chain woven goods are superfluous.
Die erfindungsgemäß anzuwendenden wäßrigen Lösungen mit den angegebenen drei Komponenten können auch zusätzlich noch geringe Mengen nativer Stärke enthalten: man erzielt dann eine erhöhte Steife des Gewebes.The aqueous solutions to be used according to the invention with the specified three components can also contain small amounts of native starch: this results in increased stiffness of the fabric.
Bemerkenswert ist noch, daß das vorgeschlagene Verfahren bei gefärbter Ware nicht zu einer Verschleierung oder Vergrauung der Färbung führt.It is also noteworthy that the proposed method does not obscure dyed goods or graying of the coloration.
Verfahren zur Herstellung
stuhlfertiger TextilgewebeMethod of manufacture
ready-to-use textile fabric
Anmelder:Applicant:
Farbenfabriken Bayer Aktiengesellschaft, Leverkusen-BayerwerkPaint factories Bayer Aktiengesellschaft, Leverkusen-Bayerwerk
Dr. Herbert Gensei und Hans Herx, Leverkusen,
sind als Erfinder genannt wordenDr. Herbert Gensei and Hans Herx, Leverkusen,
have been named as inventors
Eine Webkette, die auf 1 cm 50 Fäden Viskosereyon vom Titer 100 den enthält, wird auf einer Zylindertrockenschlichtemaschine durch Tauchen und Abquetschen mit einer 40° C warmen Lösung behandelt, die im Liter 10 g Polyacrylsäureamid, 10 g Dimethylolharnstoff und 6g Ammoniumnitrat enthält; anschließend wird die Kette stufenweise zunächst unterhalb 100° C getrocknet und dann kurz auf 110° C nacherhitzt. Die Kette läßt sich ohne Schwierigkeiten z.B. zu einem Futterstoff verweben; der Futterstoff besitzt dann eine leichte Steifheit, die waschbeständig ist, und zeigt in der Kettrichtung nur eine geringe Restkrumpfung nach dem Befeuchten.A warp which contains 50 threads of viscose rayon with a titer of 100 denier per 1 cm is placed on a cylinder dry sizing machine treated by dipping and squeezing with a 40 ° C solution, which contains 10 g of polyacrylic acid amide, 10 g of dimethylolurea and 6 g of ammonium nitrate per liter; afterward the chain is first dried in stages below 100 ° C and then briefly to 110 ° C reheated. The chain can be woven into a lining, for example, without difficulty; the lining then has a slight stiffness which is washable and shows only a slight stiffness in the warp direction Residual shrinkage after wetting.
Eine buntfarbige Webkette, die auf 1 cm 40 Fäden einfaches Baumwollgarn von der metrischen Nummer 30 enthält, wird auf einer Lufttrockenschlichtemaschine mit einer Lösung behandelt, die im Liter 6 g Polyacrylsäureamid, 20 g Kartoffelmehl, 15 g Dimethylolharnstoff und 6 g Milchsäure enthält. Anschließend wird die Kette bei etwa 70° C getrocknet. Hierauf wird die Kette zu einem Schürzenstoff verwebt, und der Stoff wird dann 3 Minuten auf 130° C erwärmt. Der Schürzenstoff besitzt einen vollen, leicht steifen Griff, der gegen wiederholte Wäsche sehr beständig ist.A brightly colored woven warp made on 1 cm of 40 threads of simple cotton yarn with the metric number 30 is treated on an air-dry sizing machine with a solution that contains 6 g Contains polyacrylic acid amide, 20 g potato flour, 15 g dimethylolurea and 6 g lactic acid. Afterward the chain is dried at about 70 ° C. The chain is then woven into an apron fabric, and the fabric is then heated to 130 ° C for 3 minutes. The apron fabric has a full, light look stiff handle that is very resistant to repeated washing.
Vor dem bekannten Verfahren zur Herstellung stuhlfertiger Gewebe, bei welchem neben zur Bildung von Carbamidharzen befähigten Methylolverbindungen Ammonium- bzw. Aminsalze von Styrol-Maleinsäure-Mischpolymerisaten zur Anwendung gelangen, weist das Verfahren der vorliegenden Erfindung den Vorteil auf. daß hierbei eine Belästigung durch Ammoniak oder Amine, die bei dem bekannten Verfahren während des Ansetzens der Lösungen und besondersBefore the known method of making chair-ready fabric, in which in addition to forming methylol compounds capable of carbamide resins ammonium or amine salts of styrene-maleic acid copolymers are used, the method of the present invention has the advantage on. that this is a nuisance by ammonia or amines, which during the known process the preparation of the solutions and especially
709 959/397709 959/397
während des Trocknens der behandelten Ware leicht auftreten kann, nicht mehr zu gewärtigen ist. Gegenüber solchen bekannten Verfahren zur Herstellung stuhlfertiger Gewebe, die auf der Grundlage von Stärke, Celluloseäthern oder Polyacrylsäureestern vorgenommen werden, zeichnet sich das erfindungsgemäße Verfahren dadurch aus, daß es zu Appreturen von besonders hoher Waschbeständigkeit führt und gleichzeitig die Krumpffestigkeit der Gewebe in Kettrichtung wesentlich verbessert.can easily occur during the drying of the treated goods, can no longer be expected. Opposite to such known processes for the production of ready-to-chair fabrics based on starch, Cellulose ethers or polyacrylic acid esters are made, the process according to the invention is distinguished characterized in that it leads to finishes of particularly high wash resistance and at the same time the resistance to shrinkage of the fabric in the warp direction is significantly improved.
Claims (1)
Deutsche Patentschrift Nr. 895 436;
französische Patentschriften Nr. 815 908, 827 059; USA.-Patentschrift Nr. 2 469 408.Considered publications:
German Patent No. 895,436;
French Patent Nos. 815 908, 827 059; U.S. Patent No. 2,469,408.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF13880A DE1027630B (en) | 1954-02-10 | 1954-02-10 | Process for the production of textile fabrics ready for use |
FR1118663D FR1118663A (en) | 1954-02-10 | 1955-02-03 | Manufacture of finished fabrics falling from the loom |
GB378055A GB788945A (en) | 1954-02-10 | 1955-02-08 | Process for the manufacture of loom-finished textile fabric |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF13880A DE1027630B (en) | 1954-02-10 | 1954-02-10 | Process for the production of textile fabrics ready for use |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1027630B true DE1027630B (en) | 1958-04-10 |
Family
ID=7087431
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEF13880A Pending DE1027630B (en) | 1954-02-10 | 1954-02-10 | Process for the production of textile fabrics ready for use |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE1027630B (en) |
FR (1) | FR1118663A (en) |
GB (1) | GB788945A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1064784A (en) * | 1972-11-01 | 1979-10-23 | Frederick C.B.M. Oliver | Resinated warp yarns for making woven fabrics for use in the production of permanent-press garments and processes of producing such yarns |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR815908A (en) * | 1935-10-28 | 1937-07-26 | Rohm & Haas Ag | Process for preparing methacrylic amide |
FR827059A (en) * | 1936-09-26 | 1938-04-15 | Ig Farbenindustrie Ag | Nitrogenous condensation products and process for preparing them |
US2469408A (en) * | 1945-12-01 | 1949-05-10 | Monsanto Chemicals | Treatment of textile material |
DE895436C (en) * | 1944-01-27 | 1953-11-02 | Basf Ag | Process for upgrading cellulose and cellulose-containing fiber material |
-
1954
- 1954-02-10 DE DEF13880A patent/DE1027630B/en active Pending
-
1955
- 1955-02-03 FR FR1118663D patent/FR1118663A/en not_active Expired
- 1955-02-08 GB GB378055A patent/GB788945A/en not_active Expired
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR815908A (en) * | 1935-10-28 | 1937-07-26 | Rohm & Haas Ag | Process for preparing methacrylic amide |
FR827059A (en) * | 1936-09-26 | 1938-04-15 | Ig Farbenindustrie Ag | Nitrogenous condensation products and process for preparing them |
DE895436C (en) * | 1944-01-27 | 1953-11-02 | Basf Ag | Process for upgrading cellulose and cellulose-containing fiber material |
US2469408A (en) * | 1945-12-01 | 1949-05-10 | Monsanto Chemicals | Treatment of textile material |
Also Published As
Publication number | Publication date |
---|---|
GB788945A (en) | 1958-01-08 |
FR1118663A (en) | 1956-06-08 |
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