CH402800A - Process for treating acrylic textile fibers, with a view to improving their whiteness - Google Patents

Process for treating acrylic textile fibers, with a view to improving their whiteness

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Publication number
CH402800A
CH402800A CH75863A CH75863A CH402800A CH 402800 A CH402800 A CH 402800A CH 75863 A CH75863 A CH 75863A CH 75863 A CH75863 A CH 75863A CH 402800 A CH402800 A CH 402800A
Authority
CH
Switzerland
Prior art keywords
fibers
acrylonitrile
bath
sub
acid
Prior art date
Application number
CH75863A
Other languages
French (fr)
Other versions
CH75863A4 (en
Original Assignee
Monsanto Chemicals
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Publication date
Application filed by Monsanto Chemicals filed Critical Monsanto Chemicals
Publication of CH75863A4 publication Critical patent/CH75863A4/xx
Publication of CH402800A publication Critical patent/CH402800A/en

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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
    • D06P5/00Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
    • D06P5/22Effecting variation of dye affinity on textile material by chemical means that react with the fibre
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F11/00Chemical after-treatment of artificial filaments or the like during manufacture
    • D01F11/04Chemical after-treatment of artificial filaments or the like during manufacture of synthetic polymers
    • D01F11/06Chemical after-treatment of artificial filaments or the like during manufacture of synthetic polymers of macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/02Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/18Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of unsaturated nitriles, e.g. polyacrylonitrile, polyvinylidene cyanide
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/28Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/38Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising unsaturated nitriles as the major constituent
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/44Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
    • D01F6/54Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polymers of unsaturated nitriles
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/68Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with phosphorus or compounds thereof, e.g. with chlorophosphonic acid or salts thereof
    • D06M11/70Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with phosphorus or compounds thereof, e.g. with chlorophosphonic acid or salts thereof with oxides of phosphorus; with hypophosphorous, phosphorous or phosphoric acids or their salts
    • 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
    • D06P1/44General 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
    • D06P1/673Inorganic compounds
    • D06P1/67316Acids
    • 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
    • D06P3/70Material containing nitrile groups
    • D06P3/76Material containing nitrile groups using basic dyes

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Inorganic Chemistry (AREA)
  • Artificial Filaments (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Description

  

  Procédé de traitement de     fibres        textiles    acryliques,  en vue d'en améliorer la blancheur    La présente invention concerne un procédé de  traitement de fibres textiles acryliques, en vue d'en  améliorer la blancheur et de favoriser sur celles-ci  la fixation des colorants basiques ; elle concerne no  tamment le traitement des fibres textiles composées  de polymères, de copolymères, de     terpolymères    et       d'interpolymères    d'ordre plus élevé d'acrylonitrile  ainsi que de mélanges de     ceux-ci.     



  Au cours de leurs productions la plupart des  fibres acryliques acquièrent un léger reflet jaunâtre  ou une couleur jaunâtre qui est regrettable. On a  proposé de nombreuses méthodes pour éliminer cette  coloration gênante. On a utilisé entre autres les  agents     blanchissants        utilisés    classiquement     dans    l'in  dustrie textile mais cela sans succès, en ce sens que,  bien que ces méthodes classiques de blanchiment  aient éliminé des défauts de coloration initiaux, les  fibres ainsi traitées ne sont pas stable à la lumière  ultraviolette ; on retrouve généralement cette colora  tion indésirable après à peu près 2 heures d'expo  sition.

   De plus des températures voisines de 1500 C  ou supérieures à celle-ci, tendent à augmenter cette  coloration des fibres textiles acryliques. On a égale  ment proposé     d'effectuer    d'abord un traitement acide  (phosphorique,     pyrophosphorique)    puis un traitement  au chlorite (brevet français No 1205810).  



  La présente invention fournit des fibres textiles  acryliques présentant une blancheur acceptable, gar  dant cette blancheur lorsqu'elles sont exposées à la  lumière ultraviolette et à la chaleur et prenant plus  facilement les teintures basiques.  



  Le     procédé    selon l'invention est caractérisé en  ce qu'on traite les fibres avec un bain comprenant  de l'acide hypophosphoreux ou un mélange d'acide    hypophosphoreux et d'au moins un de ses sels mé  talliques.  



  On peut, par exemple,     traiter    les     fibres    par une  solution aqueuse d'acide hypophosphoreux dont la       concentration        peut        aller        de        0,01%,    à     environ        1,0        0/0,     avec une concentration optimum comprise entre       0,1%        et        0,5        0%    ;

       il        est        évident        que        l'on        peut        em-          ployer    des concentrations plus élevées de l'acide,  mais cela ne présente aucun intérêt économique.

   On  peut, outre l'acide indiqué ci-dessus, utiliser un mé  lange aqueux de l'acide et de ses sels métalliques  solubles dans l'eau,     comme    par exemple les sels mé  talliques     alcalins    et alcalino-terreux hydrosolubles de  l'acide     hypophosphoreux,    en quantité nécessaire pour  maintenir la concentration des ions     hypophosphite     telle qu'elle est .donnée plus haut. Le pH de la solu  tion est maintenu à 7 ou au-dessous, avec un pH  optimum inférieur à 4. Cette solution     peut    âtre  appliquée sur les fibres par pulvérisation, en em  ployant des mèches ou des rouleaux, ou par n'im  porte quelle méthode convenable.  



  Les fibres     traitées    peuvent être en     homopoly-          mères    ou en copolymères de l'acrylonitrile, par exem  ple en copolymères     binaires,    ternaires ou d'un ordre  inférieur contenant au moins 80104 en poids     d'acry-          lo-nitrile    ;

   elles peuvent être en des mélanges com  prenant du     polyacrylonitrile    ou des polymères     com-          portant        de        l'acrylonitrile,        avec    2 à     50%        d'un        autre     produit polymérisé,

   le mélange comportant un pour  centage     total    d'acrylonitrile polymérisé d'au moins       80        %        en        poids.        Bien        que        les        polymères        se        prêtant        le     mieux à la présente invention soient ceux contenant       au        moins        80%        d'acrylonitrile,

          généralement        consi-          dérés    comme les polymères     d'acrylonitrile    suscepti  bles de ,former des fibres, il est bien entendu que la      présente invention est également applicable aux fi  bres textiles acryliques contenant moins de 80 0/0  d'acrylonitrile.  



  Le polymère peut par exemple être un     copoly-          mère        constitué        de        80    à     98,%        dacrylonitrile        et        de     2 à     20%        d'un        autre        monomère        contenant        la        liai-          son    > C = C  <  et     copolymérisable    avec l'acrylo  nitrile.  



  Le polymère peut être aussi un     interpolymère     ternaire ou d'ordre plus élevé comme par exemple  des produits obtenus par     interpolymérisation    de  l'acrylonitrile avec 2 ou plus de 2 monomères autres  que l'acrylonitrile. De façon plus précise, il est pré  férable, que le polymère ternaire soit constitué  d'acrylonitrile,

   de     méthacrylonitrile    et de     2-vinylpy-          ridine.    Il y a avantage à ce que les polymères     ter-          naires        contiennent        de        80    à     98        %        d'acrylonitrile,        de     1 à     101%        de        vinylpyridine        ou        de        1-vinylimidazole,

            et        de    1 à     18        %        d'un        autre        composé        comme        le        mé-          thacrylonitrile    ou le chlorure de vinyle.  



  Le polymère peut     également    être constitué d'un  mélange de     polyacrylonitrile    ou d'un     interpolymère          binaire        comportant        de        80    à     99        %        d'acrylonitrile        et     de 1 à     200/11    d'au moins un autre composé conte  nant le groupement > C = C  < , avec 2.

   à 50 0/0  en poids du mélange d'un copolymère comportant de       10    à     70%        d'acrylonitrile        et        de        30    à     90%        d'au     moins un autre monomère polymérisable contenant  le groupement<B>>C=C < .</B> Lorsque le polymère       comporte    un mélange,

   on a intérêt à ce qu'il s'agisse  d'un mélange d'un copolymère comportant de 90 à       98        ro/o        d'acrylonitrile        et        de    2 à     10'%        d'un        autre     monomère     mono-oléfinique,    comme l'acétate de vi  nyle,

   avec une     proportion    suffisante d'un copolymère       constitué        de        10    à     70'%        d'acrylonitrile        avec        30    à       90(%        d'une        amine        hétérocyclique        tertiaire        vinyl-          substituée,    comme la     vinylpyridine    ou le     1-vinylimi-          dazole,

      de façon à obtenir un mélange susceptible  d'être teint dont le pourcentage en amine     hétérocy-          clique        tertiaire        vinylique        est        de    2 à     10%        par        rap-          port    au poids du mélange.  



  Les exemples suivants     illustrent    la présente in  vention.  



  <I>Exemple 1</I>       Des        fibres        en        un        copolymère    à     93%        d'acrylo-          nitrile        et    7     %        d'acétate        de        vinyle,        sont        traitées        en        les     faisant passer à travers 2000     ml    d'un bain addi  tionné de 40 ml d'acide hypophosphoreux concentré  à 50 0/0.

   Les fibres sont     ensuite    séchées. Les mesu  res     colorimétriques,    effectuées par réflexion sur un  spectrophotomètre de     General        Electrie,    donnent une  pureté de 2,2 et une brillance de 85,1 ; à     partir    de  la pureté et de la brillance, on calcule que la blan  cheur est de 89,8.  



  <I>Exemple 2</I>       Des        fibres        en        un        copolymère    à     93        %        d'acrylo-          nitrile        et    7     %        d'acétate        de        vinyle        sont        traitées        en        les     faisant passer à travers 2000 ml d'un bain additionné         de    8     ml    

      d'acide        hypophosphoreux        concentré    à     50        %.     Les fibres sont ensuite séchées. Dans les conditions  indiquées dans l'exemple 1, leur pureté est de 3,2,  leur brillance de 85,2. et leur blancheur de 82,9.  



  <I>Exemple 3</I>       Des        fibres        en        un        copolymère    à     93        %        d'acryloni-          trile        et    7     %        d'acétate        de        vinyle        sont        traitées        en        les     faisant passer à travers 2000 ml d'un bain     addi-          tionné     <RTI  

   ID="0002.0177">   de        40        ml        d'acide        hypophosphoreux    à     50        %        et     4 g     d'hypophosphite    de sodium. Les fibres sont en  suite séchées. Dans les conditions données dans  l'exemple 1, on constate que leur pureté est de 1,9,  leur brillance de 84,1 et leur blancheur de 90,6.  



  <I>Exemple 4</I>       Des        fibres        en        un        copolymère    à     93:%        d'acrylo-          nitrile        et    7     %        d'acétate        de        vinyle        sont        traitées        en        les     faisant passer à travers 2000 ml d'un bain additionné       de    8     ml        

  d'acide        hypophosphoreux    à     50        %        et        20        g          d'hypophosphite    de sodium. Les fibres sont ensuite  séchées. Dans les conditions indiquées dans l'exem  ple 1, leur pureté est de 3,9, leur brillance de 85,3  et leur blancheur de 77,0.  



  <I>Exemple 5</I>  Des fibres en un copolymère à 93 'Vo     d'acrylo-          nitrile        et        7'%        d'acétate        de        vinyle        sont        traitées        en     les faisant passer à travers 2000 ml d'un bain     addi-          tionné        de    8     ml        d'acide        hypophosphoreux    à     50        %        et   

    4 g     d'hypop-hosphite    de sodium. Les fibres sont en  suite séchées. Dans les conditions indiquées dans  l'exemple 1, leur pureté est de 3,5, leur brillance de  85,6 et leur blancheur de 80,5.  



  <I>Exemple 6</I>       Des        fibres        en        un        copolymère    à     93        %        d'acrylo-          nitrile        et        7'%     d'acétate        de        vinyle        sont        traitées        en        les     faisant passer à travers 2000 ml d'un bain additionné  de 4 ml d'acide hypophosphoreux à 50% et     20#g      

      d'hypophosphite    de sodium. Les fibres sont ensuite  séchées puis teintes avec     Sevron    Blue 2G,     C.I.    Basic  Blue 22.. La     proportion    de fixation des colorants  basiques est de     6,01%    alors qu'elle n'est que de       3,71%        sans        le        traitement        conforme    à     la        présente        in-          vention.     



  Ainsi les agents de traitement propres à la pré  sente invention permettent non seulement d'obtenir  des fibres plus blanches que dans le passé, mais on  obtient en plus une augmentation de l'absorption des  colorants basiques. Le procédé conforme à la pré  sente invention confère ainsi de meilleures qualités  tinctoriales ainsi qu'une meilleure coloration des fi  bres, ce qui a pour effet d'améliorer la coloration  après teinture.



  Process for treating acrylic textile fibers, with a view to improving their whiteness The present invention relates to a process for treating acrylic textile fibers, with a view to improving their whiteness and promoting the fixing of basic dyes thereon; it relates in particular to the treatment of textile fibers composed of polymers, copolymers, terpolymers and higher-order interpolymers of acrylonitrile, as well as mixtures thereof.



  During their production most acrylic fibers acquire a slight yellowish sheen or a yellowish color which is unfortunate. Numerous methods have been proposed to eliminate this troublesome staining. The bleaching agents conventionally used in the textile industry have been used, among others, but without success, in the sense that, although these conventional bleaching methods have eliminated initial coloring defects, the fibers thus treated are not stable at ultraviolet light; this unwanted color is usually found after about 2 hours of exposure.

   In addition, temperatures close to 1500 ° C. or higher than this tend to increase this coloring of the acrylic textile fibers. It has also been proposed to carry out first an acid treatment (phosphoric, pyrophosphoric) then a treatment with chlorite (French patent No. 1205810).



  The present invention provides acrylic textile fibers exhibiting acceptable whiteness, maintaining that whiteness when exposed to ultraviolet light and heat and more readily absorbing basic dyes.



  The process according to the invention is characterized in that the fibers are treated with a bath comprising hypophosphorous acid or a mixture of hypophosphorous acid and at least one of its metal salts.



  It is possible, for example, to treat the fibers with an aqueous solution of hypophosphorous acid, the concentration of which can range from 0.01% to approximately 1.0%, with an optimum concentration of between 0.1% and 0, 50%;

       It is obvious that higher concentrations of the acid can be employed, but this is of no economic benefit.

   In addition to the acid indicated above, it is possible to use an aqueous mixture of the acid and its water-soluble metal salts, such as, for example, the water-soluble alkali and alkaline-earth metal salts of hypophosphorous acid. , in an amount necessary to maintain the concentration of the hypophosphite ions as given above. The pH of the solution is maintained at 7 or below, with an optimum pH below 4. This solution can be applied to the fibers by spraying, using wicks or rolls, or by any type. suitable method.



  The treated fibers can be in homopolymers or in copolymers of acrylonitrile, for example in binary, ternary or lower order copolymers containing at least 80104 by weight of acrylonitrile;

   they can be in mixtures comprising polyacrylonitrile or polymers comprising acrylonitrile, with 2 to 50% of another polymerized product,

   the mixture comprising a total percentage of polymerized acrylonitrile of at least 80% by weight. Although the polymers which lend themselves best to the present invention are those containing at least 80% acrylonitrile,

          Generally considered as acrylonitrile polymers capable of forming fibers, it is understood that the present invention is also applicable to acrylic textile fibers containing less than 80% of acrylonitrile.



  The polymer may, for example, be a copolymer consisting of 80 to 98% acrylonitrile and 2 to 20% of another monomer containing the> C = C <bond and copolymerizable with acrylonitrile.



  The polymer can also be a ternary or higher-order interpolymer, such as, for example, products obtained by interpolymerization of acrylonitrile with 2 or more than 2 monomers other than acrylonitrile. More precisely, it is preferable that the ternary polymer consists of acrylonitrile,

   of methacrylonitrile and 2-vinylpy- ridine. It is advantageous that the terminal polymers contain 80 to 98% acrylonitrile, 1 to 101% vinylpyridine or 1-vinylimidazole,

            and from 1 to 18% of another compound such as methacrylonitrile or vinyl chloride.



  The polymer can also consist of a mixture of polyacrylonitrile or of a binary interpolymer comprising from 80 to 99% of acrylonitrile and from 1 to 200/11 of at least one other compound containing the group> C = C < , with 2.

   at 50% by weight of the mixture of a copolymer comprising from 10 to 70% acrylonitrile and from 30 to 90% of at least one other polymerizable monomer containing the group <B>> C = C <. </ B> When the polymer contains a mixture,

   it is advantageous that it is a mixture of a copolymer comprising from 90 to 98 ro / o of acrylonitrile and from 2 to 10 '% of another mono-olefinic monomer, such as acetate vinyl,

   with a sufficient proportion of a copolymer consisting of 10 to 70% acrylonitrile with 30 to 90 (% of a vinyl-substituted tertiary heterocyclic amine, such as vinylpyridine or 1-vinylimidazole,

      so as to obtain a mixture capable of being dyed in which the percentage of vinyl tertiary heterocyclic amine is 2 to 10% relative to the weight of the mixture.



  The following examples illustrate the present invention.



  <I> Example 1 </I> Fibers in a copolymer of 93% acrylonitrile and 7% vinyl acetate, are treated by passing them through 2000 ml of an additional 40 ml bath. of 50% concentrated hypophosphorous acid.

   The fibers are then dried. The colorimetric measurements, carried out by reflection on a General Electrie spectrophotometer, give a purity of 2.2 and a brightness of 85.1; from the purity and brightness, the whiteness is calculated to be 89.8.



  <I> Example 2 </I> Fibers in a copolymer of 93% acrylonitrile and 7% vinyl acetate are treated by passing them through 2000 ml of a bath added to 8 ml

      50% concentrated hypophosphorous acid. The fibers are then dried. Under the conditions indicated in Example 1, their purity is 3.2 and their brightness is 85.2. and their whiteness of 82.9.



  <I> Example 3 </I> Fibers of a copolymer of 93% acrylonitrile and 7% vinyl acetate are treated by passing them through 2000 ml of an additive bath <RTI

   ID = "0002.0177"> 40 ml of 50% hypophosphorous acid and 4 g of sodium hypophosphite. The fibers are then dried. Under the conditions given in Example 1, it is found that their purity is 1.9, their brightness 84.1 and their whiteness 90.6.



  <I> Example 4 </I> Fibers in a 93% copolymer:% acrylonitrile and 7% vinyl acetate are treated by passing them through 2000 ml of a bath to which 8 ml has been added.

  50% hypophosphorous acid and 20 g of sodium hypophosphite. The fibers are then dried. Under the conditions indicated in Example 1, their purity is 3.9, their brightness is 85.3 and their whiteness is 77.0.



  <I> Example 5 </I> Fibers of a copolymer of 93% acrylonitrile and 7% vinyl acetate are treated by passing them through 2000 ml of a bath with addition of 8 ml of 50% hypophosphorous acid and

    4 g of sodium hypophosphite. The fibers are then dried. Under the conditions indicated in Example 1, their purity is 3.5, their brightness 85.6 and their whiteness 80.5.



  <I> Example 6 </I> Fibers of a copolymer of 93% acrylonitrile and 7% vinyl acetate are treated by passing them through 2000 ml of a bath supplemented with 4 ml of 50% hypophosphorous acid and 20 # g

      of sodium hypophosphite. The fibers are then dried and then dyed with Sevron Blue 2G, CI Basic Blue 22 .. The proportion of fixing of the basic dyes is 6.01% whereas it is only 3.71% without the treatment in accordance with the present invention.



  Thus, the treatment agents specific to the present invention not only make it possible to obtain fibers which are whiter than in the past, but also an increase in the absorption of basic dyes is obtained. The process in accordance with the present invention thus confers better dyeing qualities as well as better coloring of the fibers, which has the effect of improving the coloring after dyeing.

 

Claims (1)

REVENDICATION Procédé de traitement de fibres textiles acryli ques, en vue d'en améliorer la blancheur et de favo riser sur celles-ci la fixation des colorants basiques, caractérisé en ce que l'on traite les fibres avec un bain comprenant de l'acide hypophosphoreux ou un mélange de cet acide avec au moins un de ses sels métalliques hydrosolubles. SOUS-REVENDICATIONS 1. Procédé selon la revendication, caractérisé en ce que l'on emploie des mélanges d'acide hypophos- phoreux avec au moins un de ses sels métalliques hydrosolubles. 2. CLAIM Process for the treatment of acrylic textile fibers, with a view to improving their whiteness and promoting the fixing of basic dyes thereon, characterized in that the fibers are treated with a bath comprising acid hypophosphorous or a mixture of this acid with at least one of its water-soluble metal salts. SUB-CLAIMS 1. Process according to claim, characterized in that mixtures of hypophosporous acid with at least one of its water-soluble metal salts are employed. 2. Procédé selon la revendication, caractérisé en ce que l'on traite des fibres blanches constituées d'au moins 80 % d'acrylonitrile et de jusqu'à 20'% d'un autre monomère mono-oléfinique copolymérisable. 3. Process according to claim, characterized in that white fibers consisting of at least 80% acrylonitrile and up to 20% of another copolymerizable mono-olefinic monomer are treated. 3. Procédé selon la revendication, caractérisé en ce que l'on traite des fibres blanches constituées de 93 % d'acrylonitrile et de 7 % d'acétate de vinyle. 4. Procédé selon la sous-revendication 3, carac térisé en ce que l'on opère à un pH inférieur à 7. 5. Procédé selon la sous-revendication 4, carac térisé en ce que l'on opère avec un bain d'acide hypophosphoreux. 6. Process according to claim, characterized in that white fibers consisting of 93% acrylonitrile and 7% vinyl acetate are treated. 4. Method according to sub-claim 3, charac terized in that one operates at a pH below 7. 5. Method according to sub-claim 4, charac terized in that one operates with a bath of hypophosphorous acid. 6. Procédé selon la sous-revendication 4, carac térisé en ce que l'on opère avec un bain compre nant un mélange d'acide hypophosphoreux et d'hypo- phosphite de sodium. 7. Procédé selon la sous-revendication 4, carac térisé en ce que l'on opère avec un bain compre nant un mélange d'acide hypophosphoreux et d'hy- pophosphite de potassium. 8. Procédé selon la sous-revendication 4, carac térisé en ce que l'on opère avec un bain comprenant un mélange d'acide hypophosphoreux et d'hypophos- phite de calcium. Process according to sub-claim 4, characterized in that one operates with a bath comprising a mixture of hypophosphorous acid and sodium hypophosphite. 7. Method according to sub-claim 4, characterized in that one operates with a bath comprising a mixture of hypophosphorous acid and potassium hypophosphite. 8. Process according to sub-claim 4, characterized in that the operation is carried out with a bath comprising a mixture of hypophosphorous acid and calcium hypophosphite.
CH75863A 1962-01-26 1963-01-23 Process for treating acrylic textile fibers, with a view to improving their whiteness CH402800A (en)

Applications Claiming Priority (2)

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US16911462A 1962-01-26 1962-01-26
US23645462A 1962-11-08 1962-11-08

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CH75863A4 CH75863A4 (en) 1965-06-15
CH402800A true CH402800A (en) 1966-05-31

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CH1365563A CH447471A (en) 1962-01-26 1963-11-07 Process for manufacturing a white thermoplastic fiber

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DE (2) DE1297282B (en)
DK (1) DK113943B (en)
GB (2) GB998677A (en)
LU (1) LU44758A1 (en)
NL (2) NL288198A (en)
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JPS496799B1 (en) * 1970-12-29 1974-02-16
GB2567456B (en) 2017-10-12 2021-08-11 Si Group Switzerland Chaa Gmbh Antidegradant blend

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US2510777A (en) * 1946-12-30 1950-06-06 Du Pont Polyamide treated with a hypophosphorous acid compound
DE1096542B (en) * 1952-07-17 1961-01-05 Benckiser Gmbh Joh A Process for the finishing of fully synthetic nitrogen-containing fibers

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CH75863A4 (en) 1965-06-15
LU44758A1 (en) 1964-05-05
DE1302037B (en) 1969-10-16
DK113943B (en) 1969-05-12
SE317771B (en) 1969-11-24
GB1058229A (en) 1967-02-08
CH447471A (en) 1967-11-30
BE639717A (en)
GB998677A (en) 1965-07-21
BE627600A (en)
NL300230A (en)
DE1297282B (en) 1969-06-12
NL288198A (en)

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