BE352614A - - Google Patents
Info
- Publication number
- BE352614A BE352614A BE352614DA BE352614A BE 352614 A BE352614 A BE 352614A BE 352614D A BE352614D A BE 352614DA BE 352614 A BE352614 A BE 352614A
- Authority
- BE
- Belgium
- Prior art keywords
- bases
- salts
- isocyclic
- dyeing
- ethers
- Prior art date
Links
- 239000000975 dye Substances 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 4
- 239000011780 sodium chloride Substances 0.000 claims description 4
- 238000004043 dyeing Methods 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 239000000980 acid dye Substances 0.000 claims description 2
- 229920002678 cellulose Polymers 0.000 claims description 2
- 239000001913 cellulose Substances 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 150000002170 ethers Chemical class 0.000 claims description 2
- 239000000835 fiber Substances 0.000 claims description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N Cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 3
- LKWOOKWVBNSLGN-UHFFFAOYSA-N 2,3-dimethylcyclohexan-1-amine Chemical class CC1CCCC(N)C1C LKWOOKWVBNSLGN-UHFFFAOYSA-N 0.000 description 1
- JYDYHSHPBDZRPU-UHFFFAOYSA-N 3-methylcyclohexan-1-amine Chemical compound CC1CCCC(N)C1 JYDYHSHPBDZRPU-UHFFFAOYSA-N 0.000 description 1
- 229920002955 Art silk Polymers 0.000 description 1
- MCZVRBLCRZWFJH-UHFFFAOYSA-N Bismark brown Y Chemical compound Cl.Cl.NC1=CC(N)=CC=C1N=NC1=CC=CC(N=NC=2C(=CC(N)=CC=2)N)=C1 MCZVRBLCRZWFJH-UHFFFAOYSA-N 0.000 description 1
- 229920002301 Cellulose acetate Polymers 0.000 description 1
- 240000001194 Heliotropium europaeum Species 0.000 description 1
- XTUVJUMINZSXGF-UHFFFAOYSA-N N-methylcyclohexylamine Chemical compound CNC1CCCCC1 XTUVJUMINZSXGF-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- SQHOAFZGYFNDQX-UHFFFAOYSA-N ethyl-[7-(ethylamino)-2,8-dimethylphenothiazin-3-ylidene]azanium;chloride Chemical compound [Cl-].S1C2=CC(=[NH+]CC)C(C)=CC2=NC2=C1C=C(NCC)C(C)=C2 SQHOAFZGYFNDQX-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- UPKAWFACSJWKND-ZXFFUEEESA-J tetrasodium;(6E)-4-amino-6-[[4-[4-[(2Z)-2-(8-amino-1-oxo-5,7-disulfonatonaphthalen-2-ylidene)hydrazinyl]-3-methoxyphenyl]-2-methoxyphenyl]hydrazinylidene]-5-oxonaphthalene-1,3-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].C\1=CC2=C(S([O-])(=O)=O)C=C(S([O-])(=O)=O)C(N)=C2C(=O)C/1=N/NC(C(OC)=C1)=CC=C1C1=CC=C(N\N=C\2C(C3=C(N)C(=CC(=C3C=C/2)S([O-])(=O)=O)S([O-])(=O)=O)=O)C(OC)=C1 UPKAWFACSJWKND-ZXFFUEEESA-J 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- D06P1/64—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 using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
- D06P1/642—Compounds containing nitrogen
- D06P1/6426—Heterocyclic compounds
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<Desc/Clms Page number 1>
"Procédé de teinture d'esters ou d'éthers de la cellulose"
La présente invention concède un procédé nouveau pour la teinture dealers ou d'éthers de la cellulose..
Il consiste à additionner au bain de teinture des bases isocycliques ou leur)? sels.
On emploi comme produits auxilaires de teinture l'hexahydroaniline et ses produits de substitution comme par exemple l'hexahydrométhylaniline, l'hexa-
<Desc/Clms Page number 2>
EMI2.1
hydroéthylaniline, et aussi les homo loges de lhexa- hydroaniline,par exemple les he.xaYpdratoluidines , comme l'hexahydrcithy2-o-taluidinc et lhexahydro-m- toluidine, les hexahydroxylidines p.e. l'hexahydro- m-xylindine, et enfin les naphtylènediamines hydrogénées
EMI2.2
p.e. 1,5 ou 1,7-naphtyànoàiearinea.
Au lieu d'additionner les bases on peut aussi isoler les sels des colorants acides avec les bases et teindre la fibre avec ces composés à la manière usuelle.
EXEMPLE 1:
Dissoudre 0,1 g du sel sodique de l'acide
EMI2.3
l-amino-4-hexahydroanilidoanthraquinone-2-sulfonique en 100 cm2 d'eau. Additionner à la solution chaude de 60 - 70 1 g de la hexahydroaniline et teindre la soie artificielle à ltacétate de cellulose à une température de 65 - 75 0 ,pendant un heure environ.
Après le rinçage et le séchage la soie est teinte en des nuances pures bleues.
E X E M P L. E 2:
EMI2.4
Orange II (voie Schtatz "9arbs%offtabellen* - édition VI 1923 No.145) est teinte de la même manière.
On obtient des nuances plus foncées que sans addition de bases isocycliques.
D'autres colorants appropriée peuvent être employés,tels que Benzobrun G,, Rouge Rhoduline N0, Bleu Méthylène nouveau, Brun Bismarck Fr extra. Violet
EMI2.5
Rhoduline brillant R, Héliotrope Rhodul1ne !Bl8UJ
<Desc/Clms Page number 3>
Méthylène BB, Saframine FF extra etc.
<Desc / Clms Page number 1>
"Process for dyeing esters or ethers of cellulose"
The present invention concedes a new process for dyeing dealers or cellulose ethers.
It consists in adding isocyclic bases or their) to the dye bath? salts.
Hexahydroaniline and its substitutes such as, for example, hexahydromethylaniline, hexa-
<Desc / Clms Page number 2>
EMI2.1
hydroethylaniline, and also homo loges of hexahydroaniline, for example he.xaYpdratoluidines, such as hexahydrcithy2-o-taluidinc and hexahydro-m-toluidine, hexahydroxylidines e.g. hexahydro-m-xiamen-indaphthylatedines, and finally
EMI2.2
e.g. 1.5 or 1.7-naphthyànoàiearinea.
Instead of adding the bases, it is also possible to isolate the salts of the acid dyes with the bases and to dye the fiber with these compounds in the usual manner.
EXAMPLE 1:
Dissolve 0.1 g of the sodium salt of the acid
EMI2.3
1-amino-4-hexahydroanilidoanthraquinone-2-sulfonic acid in 100 cm2 of water. Add to the hot solution of 60-70 1 g of hexahydroaniline and dye the artificial silk with cellulose acetate at a temperature of 65-75 0 for approximately one hour.
After rinsing and drying the silk is dyed in pure blue shades.
E X E M P L. E 2:
EMI2.4
Orange II (Schtatz way "9arbs% offtabellen * - edition VI 1923 No.145) is colored in the same way.
Darker shades are obtained than without the addition of isocyclic bases.
Other suitable dyes can be used, such as Benzobrun G ,, Rhodulin Red N0, New Methylene Blue, Bismarck Brown Fr extra. Purple
EMI2.5
Brilliant rhodulin R, Heliotrope Rhodul1ne! Bl8UJ
<Desc / Clms Page number 3>
Methylene BB, Saframine FF extra etc.
Claims (1)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE352614A true BE352614A (en) |
Family
ID=27344
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE352614D BE352614A (en) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE352614A (en) |
-
0
- BE BE352614D patent/BE352614A/fr unknown
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