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 whitenessInfo
- 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
Links
- 239000000835 fiber Substances 0.000 title claims description 31
- 238000000034 method Methods 0.000 title claims description 17
- 239000004753 textile Substances 0.000 title claims description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 title claims description 7
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 16
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims description 14
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- KWSLGOVYXMQPPX-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-2h-tetrazole Chemical compound FC(F)(F)C1=CC=CC(C2=NNN=N2)=C1 KWSLGOVYXMQPPX-UHFFFAOYSA-N 0.000 claims description 5
- 239000000981 basic dye Substances 0.000 claims description 5
- 239000000178 monomer Substances 0.000 claims description 5
- 229910001379 sodium hypophosphite Inorganic materials 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 230000001737 promoting effect Effects 0.000 claims description 2
- 229910001382 calcium hypophosphite Inorganic materials 0.000 claims 1
- 229940064002 calcium hypophosphite Drugs 0.000 claims 1
- 229910001380 potassium hypophosphite Inorganic materials 0.000 claims 1
- CRGPNLUFHHUKCM-UHFFFAOYSA-M potassium phosphinate Chemical compound [K+].[O-]P=O CRGPNLUFHHUKCM-UHFFFAOYSA-M 0.000 claims 1
- CNALVHVMBXLLIY-IUCAKERBSA-N tert-butyl n-[(3s,5s)-5-methylpiperidin-3-yl]carbamate Chemical compound C[C@@H]1CNC[C@@H](NC(=O)OC(C)(C)C)C1 CNALVHVMBXLLIY-IUCAKERBSA-N 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 description 13
- 229920000642 polymer Polymers 0.000 description 9
- -1 for example Chemical class 0.000 description 5
- 238000004040 coloring Methods 0.000 description 4
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 3
- 229920002239 polyacrylonitrile Polymers 0.000 description 3
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 2
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- RFQSMLBZXQOMKK-UHFFFAOYSA-N [3-[(4,8-diamino-6-bromo-1,5-dioxonaphthalen-2-yl)amino]phenyl]-trimethylazanium;chloride Chemical compound [Cl-].C[N+](C)(C)C1=CC=CC(NC=2C(C3=C(N)C=C(Br)C(=O)C3=C(N)C=2)=O)=C1 RFQSMLBZXQOMKK-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910001919 chlorite Inorganic materials 0.000 description 1
- 229910052619 chlorite group Inorganic materials 0.000 description 1
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
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
- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
- D06P5/22—Effecting variation of dye affinity on textile material by chemical means that react with the fibre
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F11/00—Chemical after-treatment of artificial filaments or the like during manufacture
- D01F11/04—Chemical after-treatment of artificial filaments or the like during manufacture of synthetic polymers
- D01F11/06—Chemical 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
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/18—Monocomponent 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
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/28—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/38—Monocomponent 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
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/44—Monocomponent 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
- D01F6/54—Monocomponent 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
-
- 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
- D06M11/00—Treating 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
- D06M11/68—Treating 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
- D06M11/70—Treating 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
-
- 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
- D06P1/673—Inorganic compounds
- D06P1/67316—Acids
-
- 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
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/70—Material containing nitrile groups
- D06P3/76—Material 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)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16911462A | 1962-01-26 | 1962-01-26 | |
US23645462A | 1962-11-08 | 1962-11-08 |
Publications (2)
Publication Number | Publication Date |
---|---|
CH75863A4 CH75863A4 (en) | 1965-06-15 |
CH402800A true CH402800A (en) | 1966-05-31 |
Family
ID=26864782
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH75863A CH402800A (en) | 1962-01-26 | 1963-01-23 | Process for treating acrylic textile fibers, with a view to improving their whiteness |
CH1365563A CH447471A (en) | 1962-01-26 | 1963-11-07 | Process for manufacturing a white thermoplastic fiber |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH1365563A CH447471A (en) | 1962-01-26 | 1963-11-07 | Process for manufacturing a white thermoplastic fiber |
Country Status (8)
Country | Link |
---|---|
BE (2) | BE639717A (en) |
CH (2) | CH402800A (en) |
DE (2) | DE1297282B (en) |
DK (1) | DK113943B (en) |
GB (2) | GB998677A (en) |
LU (1) | LU44758A1 (en) |
NL (2) | NL288198A (en) |
SE (1) | SE317771B (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS496799B1 (en) * | 1970-12-29 | 1974-02-16 | ||
GB2567456B (en) | 2017-10-12 | 2021-08-11 | Si Group Switzerland Chaa Gmbh | Antidegradant blend |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
-
0
- BE BE627600D patent/BE627600A/xx unknown
- NL NL300230D patent/NL300230A/xx unknown
- NL NL288198D patent/NL288198A/xx unknown
- BE BE639717D patent/BE639717A/xx unknown
-
1963
- 1963-01-15 GB GB181563A patent/GB998677A/en not_active Expired
- 1963-01-23 CH CH75863A patent/CH402800A/en unknown
- 1963-01-26 DE DE1963M0055568 patent/DE1297282B/en active Pending
- 1963-11-04 GB GB4345763A patent/GB1058229A/en not_active Expired
- 1963-11-05 LU LU44758D patent/LU44758A1/xx unknown
- 1963-11-07 SE SE1228463A patent/SE317771B/xx unknown
- 1963-11-07 DK DK522863A patent/DK113943B/en unknown
- 1963-11-07 CH CH1365563A patent/CH447471A/en unknown
-
1968
- 1968-11-07 DE DE1968M0058826 patent/DE1302037B/en active Pending
Also Published As
Publication number | Publication date |
---|---|
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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