EP0240461B1 - Mélanges d'agents de blanchiment optique - Google Patents
Mélanges d'agents de blanchiment optique Download PDFInfo
- Publication number
- EP0240461B1 EP0240461B1 EP87810176A EP87810176A EP0240461B1 EP 0240461 B1 EP0240461 B1 EP 0240461B1 EP 87810176 A EP87810176 A EP 87810176A EP 87810176 A EP87810176 A EP 87810176A EP 0240461 B1 EP0240461 B1 EP 0240461B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- formula
- compound
- weight
- parts
- mixture according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims description 35
- 230000003287 optical effect Effects 0.000 title description 8
- 150000001875 compounds Chemical class 0.000 claims description 54
- 229920000728 polyester Polymers 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 6
- 239000004753 textile Substances 0.000 claims description 6
- XSPWINZRSAKTKX-UHFFFAOYSA-N 3-[2-[4-[2-(4-cyanophenyl)ethenyl]phenyl]ethenyl]benzonitrile Chemical compound C1=CC(C#N)=CC=C1C=CC(C=C1)=CC=C1C=CC1=CC=CC(C#N)=C1 XSPWINZRSAKTKX-UHFFFAOYSA-N 0.000 claims description 2
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 2
- 230000002087 whitening effect Effects 0.000 claims 2
- RBABXJPJIHMBBP-WXUKJITCSA-N 2-[(e)-2-[4-[(e)-2-(2-cyanophenyl)ethenyl]phenyl]ethenyl]benzonitrile Chemical compound N#CC1=CC=CC=C1\C=C\C(C=C1)=CC=C1\C=C\C1=CC=CC=C1C#N RBABXJPJIHMBBP-WXUKJITCSA-N 0.000 claims 1
- OQVQNTRMZCGXIB-ICYHVJMASA-N 2-[(e)-2-[4-[(e)-2-(4-cyanophenyl)ethenyl]phenyl]ethenyl]benzonitrile Chemical compound C1=CC(C#N)=CC=C1\C=C\C(C=C1)=CC=C1\C=C\C1=CC=CC=C1C#N OQVQNTRMZCGXIB-ICYHVJMASA-N 0.000 claims 1
- JRVKAPLKKVWGKU-UHFFFAOYSA-N 2-[2-[4-[2-(3-cyanophenyl)ethenyl]phenyl]ethenyl]benzonitrile Chemical compound N#CC1=CC=CC(C=CC=2C=CC(C=CC=3C(=CC=CC=3)C#N)=CC=2)=C1 JRVKAPLKKVWGKU-UHFFFAOYSA-N 0.000 claims 1
- 239000006081 fluorescent whitening agent Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000004744 fabric Substances 0.000 description 5
- 238000005282 brightening Methods 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229920004933 Terylene® Polymers 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 1
- -1 1,4-bis (2-cyanstyryl) benzene 1- (2-cyanstyryl) -4- (4-cyanstyryl) benzene 1- (2-cyanstyryl) -4- (3-cyanstyryl) benzene Chemical compound 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound 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
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/60—Optical bleaching or brightening
- D06L4/65—Optical bleaching or brightening with mixtures of optical brighteners
Definitions
- Optical brighteners are often used as mixtures of two or more different types, because such mixtures show a synergistic effect in that the degree of whiteness of the mixture is higher than the degree of whiteness of the same amount of the individual components.
- the invention therefore relates to mixtures of optical brighteners composed of 1 to 99 parts by weight of a compound of the formula 1 wherein R1 and R2 are the same or different and are -CN, -COOCH3 or -COOC2H5, and 99 to 1 part by weight of one or more compounds of the formulas 2 to 10
- the mixtures preferably consist of 25 to 75 parts by weight of a compound of the formula 1 and 75 to 25 parts by weight of one or more of the compounds of the formulas 2 to 9, in particular the compounds of the formulas 3, 4 and 8, the preferred mixing ratio to the compound of the formula 8 20 to 50 to 80 to 50, while the preferred mixing ratio of a compound of formula 1 with a compound of formula 10 is 5 to 15 to 95 to 85, especially about 10 to 90 parts by weight.
- R1 and R2 are preferably the same and are especially -CN or also -COOC2H5.
- Preferred compounds of formula 10 are: 1,4-bis (2-cyanstyryl) benzene 1- (2-cyanstyryl) -4- (4-cyanstyryl) benzene 1- (2-cyanstyryl) -4- (3-cyanstyryl) benzene and 1- (3-cyanstyryl) -4- (4-cyanstyryl) benzene.
- the compounds of the formulas 2 to 10 can also be used individually in any mixture with one another together with a compound of the formula 1 as optical brighteners, the mixing ratio of the compounds of the formulas 2 to 10 to one another being uncritical and being able to be varied depending on experience.
- the mixtures according to the invention are obtained either by jointly dispersing compounds of the formula 1 with one or more compounds of the formulas 2 to 10 in the stated mixing ratio or else by separate dispersing of the components and mechanical mixing.
- the optimal mixing ratio depends on the type of connection and can be easily determined by simple tests.
- the present invention further relates to the use of mixtures of a compound of the formula 1 with one or more compounds of the formulas 2 to 10 for the optical brightening of polyester fibers and textile material containing polyester fibers, and agents for the optical brightening of polyester fibers and Textile materials containing polyester fibers, containing mixtures of a compound of formula 1 with one or more of the compounds of formulas 2 to 10.
- the mixtures according to the invention are particularly suitable for optically brightening textile materials made of linear or modified polyesters. They can be applied to the textile material by known methods, for example by the exhaust process at 90 to 140 ° C or by the pad thermal process at 160 to 220 ° C.
- the mixtures according to the invention are distinguished by very good dyeing behavior. In addition to a higher degree of whiteness compared to the corresponding proportions of the individual components, the mixtures have an improved brilliance of the brightenings.
- a polyester fabric (Terylene type 540) is at 40 ° C on a dyeing machine at a liquor ratio of 1 to 20 with an aqueous bath containing 0.1% by weight of an optical brightener from a mixture of 25 parts by weight of the compound of the formula and 75 parts by weight of the compound of the formula as well as 1 g / l of a fatty alcohol polyglycol ether (Irgasol P) treated.
- the temperature is increased to 120 ° C. within 30 minutes and left at this level for a further 30 minutes. Then you cool down to 40 ° C within 15 minutes.
- the fabric is rinsed in flowing deionized water for 30 seconds and dried at 80 ° C.
- the polyester fabric treated in this way has a high lightening effect.
- a polyester fabric (Terylene type 540) is padded at room temperature with an aqueous liquor containing 1 g / l of the brightener mixture of 50 parts by weight of the compound of the formula 1 and 50 parts by weight of the compound of the formula 4 (calculated on active substance) in dispersed form and 1 ml / l Invadin JFC 200%.
- the squeezing effect is 65%.
- polyester fabric treated in this way has a high lightening effect.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Detergent Compositions (AREA)
Claims (14)
- Mélanges selon la revendication 1, caractérisés en ce qu'ils sont constitués de 25 à 75 parties en poids d'un composé de formule 1 et de 75 à 25 parties en poids d'un ou plusieurs composés de formules 2 à 9.
- Mélanges selon la revendication 2, caractérisés en ce qu'ils sont constitués d'un composé de formule 1 et du composé de formule 3.
- Mélanges selon la revendication 2, caractérisés en ce qu'ils sont constitués d'un composé de formule 1 et du composé de formule 4.
- Mélanges selon la revendication 1, caractérisés en ce qu'ils sont constitués de 20 à 50 parties en poids d'un composé de formule 1 et de 80 à 50 parties en poids du composé de formule 8.
- Mélanges selon la revendication 1, caractérisés en ce qu'ils sont constitués de 5 à 15 parties en poids d'un composé de formule 1 et de 95 à 85 parties en poids d'un composé de formule 10.
- Mélanges selon la revendication 1, caractérisés en ce que, dans le composé de formule 1, R₁ et R₂ sont identiques.
- Mélanges selon la revendication 7, caractérisés en ce que R₁ et R₂ représentent -CN.
- Mélanges selon la revendication 6, caractérisés en ce que le composé de formule 10 est le 1,4-bis-(2-cyanostyryl)-benzène.
- Mélanges selon la revendication 6, caractérisés en ce que le composé de formule 10 est le 1-(2-cyanostyryl)-4-(4-cyanostyryl)-benzène.
- Mélanges selon la revendication 6, caractérisés en ce que le composé de formule 10 est le 1-(2-cyanostyryl)-4-(3-cyanostyryl)-benzène.
- Mélanges selon la revendication 6, caractérisés en ce que le composé de formule 10 est le 1-(3-cyanostyryl)-4-(4-cyanostyryl)-benzène.
- Utilisation de mélanges constitués d'un composé de formule 1 avec un ou plusieurs composés de formules 2 à 10 selon la revendication 1, pour l'azurage optique de fibres de polyester et de matériau textile contenant des fibres de polyester.
- Produit pour l'azurage optique de fibres de polyester et de matériau textile contenant des fibres de polyester, caractérisé en ce qu'il contient l'un des mélanges selon la revendication 1, constitué d'un composé de formule 1 et d'un ou plusieurs des composés de formules 2 à 10.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1284/86 | 1986-04-02 | ||
CH128486 | 1986-04-02 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0240461A1 EP0240461A1 (fr) | 1987-10-07 |
EP0240461B1 true EP0240461B1 (fr) | 1991-04-17 |
Family
ID=4206828
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP87810176A Expired - Lifetime EP0240461B1 (fr) | 1986-04-02 | 1987-03-27 | Mélanges d'agents de blanchiment optique |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0240461B1 (fr) |
JP (1) | JPS62236865A (fr) |
BR (1) | BR8701478A (fr) |
DE (1) | DE3769352D1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0682145A2 (fr) * | 1994-05-12 | 1995-11-15 | Ciba-Geigy Ag | Traitement textile |
US6117189A (en) * | 1994-05-12 | 2000-09-12 | Ciba Specialty Chemicals Corporation | Protective method |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU5845890A (en) * | 1989-06-22 | 1991-01-08 | Fmc Corporation | Thickened and gelled systems based on starch and glucomannan |
DE10219993A1 (de) * | 2002-05-03 | 2003-11-20 | Basf Ag | Verfahren zum Aufhellen von textilen Materialien |
DE10245705A1 (de) | 2002-09-30 | 2004-04-01 | Bayer Ag | Ein Polycarbonat oder Polyestercarbonat enthaltend optische Aufheller |
ES2316862T3 (es) * | 2002-12-10 | 2009-04-16 | Ciba Holding Inc. | Mezclas de agentes de blanqueo fluorescentes. |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH603513A5 (fr) * | 1975-02-05 | 1978-08-15 | Sandoz Ag | |
US4666627A (en) * | 1983-05-08 | 1987-05-19 | Ciba-Geigy Corporation | 4-Heterocyclylvinyl-4-'styryl-biphenyls |
-
1987
- 1987-03-27 DE DE8787810176T patent/DE3769352D1/de not_active Expired - Lifetime
- 1987-03-27 EP EP87810176A patent/EP0240461B1/fr not_active Expired - Lifetime
- 1987-04-01 BR BR8701478A patent/BR8701478A/pt unknown
- 1987-04-02 JP JP62082203A patent/JPS62236865A/ja active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0682145A2 (fr) * | 1994-05-12 | 1995-11-15 | Ciba-Geigy Ag | Traitement textile |
EP0682145A3 (fr) * | 1994-05-12 | 1998-08-26 | Ciba SC Holding AG | Traitement textile |
US6117189A (en) * | 1994-05-12 | 2000-09-12 | Ciba Specialty Chemicals Corporation | Protective method |
Also Published As
Publication number | Publication date |
---|---|
EP0240461A1 (fr) | 1987-10-07 |
BR8701478A (pt) | 1988-01-19 |
DE3769352D1 (de) | 1991-05-23 |
JPS62236865A (ja) | 1987-10-16 |
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