CH366813A - Färben und Bedrucken von textilen Gebilden aus Polyacrilnitril und acrylnitrilhaltigen Mischpolymerisaten - Google Patents
Färben und Bedrucken von textilen Gebilden aus Polyacrilnitril und acrylnitrilhaltigen MischpolymerisatenInfo
- Publication number
- CH366813A CH366813A CH7351759A CH7351759A CH366813A CH 366813 A CH366813 A CH 366813A CH 7351759 A CH7351759 A CH 7351759A CH 7351759 A CH7351759 A CH 7351759A CH 366813 A CH366813 A CH 366813A
- Authority
- CH
- Switzerland
- Prior art keywords
- dyeing
- amino
- polyacrylonitrile
- group
- acrylonitrile
- Prior art date
Links
- 238000004043 dyeing Methods 0.000 title claims description 18
- 229920002239 polyacrylonitrile Polymers 0.000 title claims description 10
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 title claims description 5
- 229920001577 copolymer Polymers 0.000 title claims description 5
- 239000004753 textile Substances 0.000 title claims description 5
- 239000000975 dye Substances 0.000 claims description 26
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 229910052717 sulfur Chemical group 0.000 claims description 4
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000004947 alkyl aryl amino group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000004104 aryloxy group Chemical group 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 2
- 150000007522 mineralic acids Chemical class 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 125000001309 chloro group Chemical group Cl* 0.000 description 5
- 239000004744 fabric Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- -1 alkylphenols Chemical class 0.000 description 4
- 125000003277 amino group Chemical group 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 239000007859 condensation product Substances 0.000 description 4
- CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000013016 damping Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 1
- DXBHBZVCASKNBY-UHFFFAOYSA-N 1,2-Benz(a)anthracene Chemical compound C1=CC=C2C3=CC4=CC=CC=C4C=C3C=CC2=C1 DXBHBZVCASKNBY-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- OHLUUHNLEMFGTQ-UHFFFAOYSA-N N-methylacetamide Chemical compound CNC(C)=O OHLUUHNLEMFGTQ-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 150000002431 hydrogen Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000007524 organic acids Chemical group 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/02—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position
- C09B5/18—Coeroxene; Coerthiene; Coeramidene; Derivatives thereof
-
- 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)
- Organic Chemistry (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF25818A DE1098910B (de) | 1958-05-24 | 1958-05-24 | Faerben und Bedrucken von geformten Gebilden aus Polyacrylnitril oder aus Mischpolymerisaten, die als wesentlichen Bestandteil Acrylnitril enthalten |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CH7351759A4 CH7351759A4 (en, 2012) | 1962-10-15 |
| CH366813A true CH366813A (de) | 1963-03-15 |
Family
ID=7091773
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH7351759A CH366813A (de) | 1958-05-24 | 1959-10-01 | Färben und Bedrucken von textilen Gebilden aus Polyacrilnitril und acrylnitrilhaltigen Mischpolymerisaten |
Country Status (2)
| Country | Link |
|---|---|
| CH (1) | CH366813A (en, 2012) |
| DE (1) | DE1098910B (en, 2012) |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE718752C (de) * | 1933-05-03 | 1942-03-19 | Ig Farbenindustrie Ag | Verfahren zur Herstellung von Farbstoffen bzw. Farbstoffzwischenprodukten |
-
1958
- 1958-05-24 DE DEF25818A patent/DE1098910B/de active Pending
-
1959
- 1959-10-01 CH CH7351759A patent/CH366813A/de unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE1098910B (de) | 1961-02-09 |
| CH7351759A4 (en, 2012) | 1962-10-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CH179075A (de) | Kapillaraktives Mittel. | |
| DE2139688A1 (de) | Farbstoffe zum faerben von kunststoffen | |
| DE2850994C2 (en, 2012) | ||
| DE1921827A1 (de) | Verfahren zur Erzeugung von Faerbungen auf Fasermaterial aus polymerem oder copolymerem Acrylnitril | |
| CH366813A (de) | Färben und Bedrucken von textilen Gebilden aus Polyacrilnitril und acrylnitrilhaltigen Mischpolymerisaten | |
| DE1928372A1 (de) | Wasserunloesliche Monoazofarbstoffe | |
| DE2122232B2 (de) | Anthrachinonverbindungen, Verfahren zu deren Herstellung und deren Verwendung | |
| DE2819197C2 (en, 2012) | ||
| DE1942508A1 (de) | Verfahren zum Faerben oder Bedrucken von Textilmaschinen aus Polymerisaten oder Mischpolymerisaten des Acrylnitrils | |
| DE2036505C3 (de) | Kationische Farbstoffe, Verfahren zu deren Herstellung und deren Verwendung | |
| DE2239445C3 (de) | Kationische Pyrazolfarbstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| DE956575C (de) | Verfahren zum Faerben und Bedrucken von Fasern aus Polyacrylnitrilen | |
| DE2851373A1 (de) | Wasserloesliche kationische monoazo- farbstoffe | |
| DE2234465C3 (de) | Farbstoffmischungen und Verfahren zum Färben und Bedrucken von Polyesterfasermaterialien | |
| DE1644322C3 (de) | Basische Monoazofarbstoffe, Verfahren zu ihrer Herstellung und deren Verwendung | |
| DE2411761A1 (de) | Basische oxazinfarbstoffe, verfahren zu ihrer herstellung und ihre verwendung | |
| DE2002916A1 (de) | Verfahren zum Faerben oder Bedrucken von Textilmaterial aus Polymerisaten oder Mischpolymerisaten des Acrylnitrils | |
| DE2901666A1 (de) | Faerbeverfahren | |
| DE2154051B2 (de) | Gelbe, wasserunlösliche Chinophthalonfarbstoffe und Farbstoff/Dispergiermittel-Gemische | |
| AT244285B (de) | Beständiges Färbepräparat | |
| DE2612740A1 (de) | Verfahren zum faerben von gemischen aus aromatischem polyester und cellulose | |
| DE1051242B (de) | Verfahren zur Erzeugung von Faerbungen auf Fasermaterialien | |
| DE1619328B1 (de) | Verwendung eines quaternisierten Benzthiazolazofarbstoffes zu Färben von Textilmaterialien aus Polyacrylnitril | |
| DE1937885A1 (de) | Basische Monoazofarbstoffe,ihre Herstellung und Verwendung | |
| CH507348A (de) | Verfahren zur Herstellung von Farbstoffen |