BE353232A - - Google Patents
Info
- Publication number
- BE353232A BE353232A BE353232DA BE353232A BE 353232 A BE353232 A BE 353232A BE 353232D A BE353232D A BE 353232DA BE 353232 A BE353232 A BE 353232A
- Authority
- BE
- Belgium
- Prior art keywords
- materials
- substances
- inorganic base
- incorporated
- anthraquinone derivatives
- Prior art date
Links
- 239000000463 material Substances 0.000 claims description 21
- 238000011282 treatment Methods 0.000 claims description 10
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 8
- 150000004056 anthraquinones Chemical class 0.000 claims description 8
- 229920002678 cellulose Polymers 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 238000004043 dyeing Methods 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 125000001769 aryl amino group Chemical group 0.000 claims description 5
- 229920002301 cellulose acetate Polymers 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 4
- 125000003282 alkyl amino group Chemical group 0.000 claims description 4
- 150000007529 inorganic bases Chemical class 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 229910021538 borax Inorganic materials 0.000 claims description 3
- 238000004040 coloring Methods 0.000 claims description 3
- 239000004744 fabric Substances 0.000 claims description 3
- 239000000835 fiber Substances 0.000 claims description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 3
- 239000004328 sodium tetraborate Substances 0.000 claims description 3
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 3
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 claims description 2
- 229910000397 disodium phosphate Inorganic materials 0.000 claims description 2
- 235000019800 disodium phosphate Nutrition 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 229940096992 potassium oleate Drugs 0.000 claims description 2
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 claims description 2
- 239000001632 sodium acetate Substances 0.000 claims description 2
- 235000017281 sodium acetate Nutrition 0.000 claims description 2
- 239000001488 sodium phosphate Substances 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- 125000005122 aminoalkylamino group Chemical group 0.000 claims 1
- 230000007062 hydrolysis Effects 0.000 claims 1
- 238000006460 hydrolysis reaction Methods 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 235000015424 sodium Nutrition 0.000 claims 1
- -1 filaments Substances 0.000 description 3
- 229920002955 Art silk Polymers 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- FBMQNRKSAWNXBT-UHFFFAOYSA-N 1,4-diaminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2N FBMQNRKSAWNXBT-UHFFFAOYSA-N 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229960004249 sodium acetate Drugs 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229940045870 sodium palmitate Drugs 0.000 description 1
- GGXKEBACDBNFAF-UHFFFAOYSA-M sodium;hexadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCC([O-])=O GGXKEBACDBNFAF-UHFFFAOYSA-M 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 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
- 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
- D06P1/653—Nitrogen-free carboxylic acids or their salts
- D06P1/6533—Aliphatic, araliphatic or cycloaliphatic
-
- 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
- D06P1/67333—Salts or hydroxides
- D06P1/6735—Salts or hydroxides of alkaline or alkaline-earth metals with anions different from those provided for in D06P1/67341
-
- 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
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/043—Material containing basic nitrogen containing amide groups using dispersed dyes
-
- 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
- D06P3/34—Material containing ester groups
- D06P3/40—Cellulose acetate
- D06P3/42—Cellulose acetate using dispersed dyestuffs
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Coloring (AREA)
Description
<Desc/Clms Page number 1>
EMI1.1
if PERF. CTIOlif.NE1:lENrS A LA COLORATION DE 1JJTI1!iREB"
Cette invention a trait au traitement de matières et spécialement de matières telles que : filaments , fi- bres, fils, tissus, films , etc..., constitués par ou contenant des esters cellulosiques , par exemple de l'acé- tate de cellulose ,du propionate de cellulose ou du buty- rate de cellulose, en vue de l'obtention de colorations solides .
On a constaté que les couleurs obtenues par la tein- ture, l'impression, le ponçage ,etc.., plus spécialement sur des matières constituées par ou contenant des esters cellulosiques fabriqués à l'aide de certains dérivés an-
<Desc/Clms Page number 2>
thraquinoniques, et plus particulièrement à l'aide de dérivés anthraquinoniques contenant des groupes amino libre ,alkylamino ou arylamino -- que ces groupes contien- nent, ou non, d'autres groupes de substitution dans le noyau , comme par exemple les groupes mercapto, pxy , alkoxy , halogène ou nitro --, ne résistent pas aux in- fluences combinées des acides et de la lumière .
Comme les traitements auxquels les matières sont soumises dans l'industrie consistent fréquemment à soumettre ces ma- tières à l'action d'acides, ce manque de solidité constitue un sérieux obstacle à l'emploi des dérivés anthraquinoni- ques, et en particulier des dérivés spécifiés en¯vue de la production de colorations, étant donné que ,dans la pratique les matières colorées sont presque toujours appelées à être exposées à la lumière ,
Suivant la présente invention, la solidité des couleurs obtenues par la teinture , l'impression , le ponçage ,etc....
spécialement sur des matières cons- tituées par ou contenant des esters cellulosiques fabri- qués à l'aide de dérivés anthraquinoniques, et plus par- ticulièrement des dérivés anthraquinoniques contenant les groupes-amino libre ,alkylamino ou arylamino , est assu- rée en supprimant toute réaction d'acide nuisible sur la fibre , le tissu ou autre matière .
Ceci peut être réalisé en rinçant ou lavant les matières , de préférence après la teinture ou autre procé- dé de coloration, jusqu'à ce que lesdites matières soient devenues à peu près ou entièrement exemptes d'acide, mais il est plus avantageux de le réaliser en incorporant aux matières ,à une phase quelconque de leur fabrication ou traitement ,et de préférence pendant la teinture
<Desc/Clms Page number 3>
ou autre procédé de coloration ou pendant un traitement de finissage ou autre traitement supplémentaire ,une ou plusieurs substances contenant une base inorganique et ayant une réaction alcaline .
De telles substances sont, par exemple ,le carbonate de sodium le borax ,le phos- phate @@@@@@@ disodique , l'acétate de sodium ,le palmitate de sodium et l'oléate de potassium, mais il est bien entendu que ces exemples ne limitent l'invention en aucune façon .
Dans le traitement de matières constituées par ou contenant des esters cellulosiques , il est préférable que les substances ne soient pas suffisamment basiques ou- alcalines ou qu'elles ne soient pas appliquées à un degré de concentration suffisant pour hydroliser dans une mesure nuisible l'ester cellulosique ,
Les exemples qui suivent feront comprendre l'in- vention, étant bien entendu toutefois qu'ils ne la limi- tent en aucune façon .
Exemple 1.- Des fils de soie artificielle d'acétate de cellulose sont d'abord teints de toute manière convena- ble par une quantité suffisante de 1.4-diaminoanthraquinone pour obtenir la nuance désirée , Après la teinture , on rin- ce la matière dans de l'eau contenant 2 grammes de borax par litre et on la sèche sans autre rinçage.
Exemple 2.- On teint de la soie artificielle d'acé- tate de cellulose sous une forme quelconque avec de la
EMI3.1
1-mono.n.éthylarnino-4-oxyanthra,uin,one, on la traite alors dans un bain contenant 3 grammes de carbonate de sodium par litre .puis on la sèche sans la rincer .
Quoiqu'on ait plus particulièrement décrit l'appli- cation de l'invention au traitement de matières constituées Par ou contenant des esters cellulosiques , comme par exem- ple l'acétate de cellulose, on remarquera que cette inven- @
<Desc/Clms Page number 4>
tion est aussi applicable au traitement de toutes'autres matières qui peuvent être teintes ou autrement colorées par des dérivés anthraquinoniques ( en particulier ceux contenant des groupes amino libre , alkylamino ou arylamino) tels que la laine, la soie naturelle, les éthers cellulosiques , etc... et au traitement de matières mixtes .
<Desc / Clms Page number 1>
EMI1.1
if PERF. CTIOlif.NE1: lENrS TO THE COLORATION OF 1JJTI1! IREB "
This invention relates to the treatment of materials and especially materials such as: filaments, fibers, threads, fabrics, films, etc., made of or containing cellulose esters, for example cellulose acetate. , cellulose propionate or cellulose butyrate, with a view to obtaining solid colorations.
It has been found that the colors obtained by dyeing, printing, sanding, etc., more especially on materials constituted by or containing cellulose esters produced with the aid of certain anti-
<Desc / Clms Page number 2>
thraquinones, and more particularly using anthraquinone derivatives containing free amino, alkylamino or arylamino groups - whether or not these groups contain other substitution groups in the nucleus, such as for example mercapto groups, pxy, alkoxy, halogen or nitro - are not resistant to the combined influence of acids and light.
As the treatments to which materials are subjected in industry frequently consist in subjecting these materials to the action of acids, this lack of solidity constitutes a serious obstacle to the use of anthraquinone derivatives, and in particular of derivatives specified for the production of colorations, since in practice colored materials are almost always required to be exposed to light,
According to the present invention, the color fastness obtained by dyeing, printing, sanding, etc.
especially on materials consisting of or containing cellulose esters manufactured using anthraquinone derivatives, and more particularly anthraquinone derivatives containing the free amino, alkylamino or arylamino groups, is ensured by removing any harmful acid reaction on fiber, fabric or other material.
This can be done by rinsing or washing the materials, preferably after dyeing or other coloring process, until said materials have become substantially or entirely acid-free, but it is more advantageous to do so. carried out by incorporating into the materials, at any phase of their manufacture or treatment, and preferably during dyeing
<Desc / Clms Page number 3>
or other coloring process or during a finishing treatment or other additional treatment, one or more substances containing an inorganic base and having an alkaline reaction.
Such substances are, for example, sodium carbonate, borax, disodium phosphate, sodium acetate, sodium palmitate and potassium oleate, but it is of course that these examples do not limit the invention in any way.
In the treatment of materials consisting of or containing cellulose esters, it is preferable that the substances are not sufficiently basic or alkaline or that they are not applied in a sufficient degree of concentration to hydrolyze the ester to an adverse extent. cellulosic,
The examples which follow will make the invention understood, it being understood, however, that they do not limit it in any way.
Example 1. - Cellulose acetate artificial silk threads are first dyed in any suitable manner with a sufficient amount of 1,4-diaminoanthraquinone to obtain the desired shade. After dyeing, the material is rinsed in water containing 2 grams of borax per liter and dried without further rinsing.
Example 2 Artificial silk of cellulose acetate in any form is dyed with
EMI3.1
1-mono.n.ethylarnino-4-oxyanthra, uin, one, it is then treated in a bath containing 3 grams of sodium carbonate per liter. Then it is dried without rinsing it.
Although the application of the invention to the treatment of materials consisting of or containing cellulose esters, such as cellulose acetate, for example, it will be noted that this invention has been more particularly described.
<Desc / Clms Page number 4>
tion is also applicable to the treatment of all other materials which may be dyed or otherwise colored by anthraquinone derivatives (especially those containing free amino, alkylamino or arylamino groups) such as wool, natural silk, cellulose ethers, etc. ... and the treatment of mixed materials.
Claims (1)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE353232A true BE353232A (en) |
Family
ID=27854
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE353232D BE353232A (en) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE353232A (en) |
-
0
- BE BE353232D patent/BE353232A/fr unknown
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