EP0074590B1 - Preparations of optical brighteners - Google Patents
Preparations of optical brighteners Download PDFInfo
- Publication number
- EP0074590B1 EP0074590B1 EP82108168A EP82108168A EP0074590B1 EP 0074590 B1 EP0074590 B1 EP 0074590B1 EP 82108168 A EP82108168 A EP 82108168A EP 82108168 A EP82108168 A EP 82108168A EP 0074590 B1 EP0074590 B1 EP 0074590B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- brightener
- denotes
- preparations
- radical
- brighteners
- 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
Links
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
- D06L4/664—Preparations of optical brighteners; Optical brighteners in aerosol form; Physical treatment of optical brighteners
Definitions
- the invention relates to brightener preparations in solid or liquid form which contain a cationic optical brightener, an anionic surfactant and optionally other additives, with the exception of those preparations which are obtained by melt formation.
- the anionic surfactants can be used in the form of the free acid or in the form of their water-soluble salts.
- inorganic salts such as NaCl, Na 2 S0 4
- Salts of organic acids for example CH 3 COONa
- readily water-soluble organic compounds such as, for example, s-caprolactam, sugar, etc.
- the concentration of the cationic optical brightener in the preferably liquid aqueous preparation is in the range from 1-10%, that of the anionic surfactants from 3 ⁇ 40% and that of the further additives likewise from 3-40%.
- the brightener preparations according to the invention are produced by homogenizing the cationic optical brighteners together with the anionic surfactants and possibly the other additives in an aqueous medium and, if necessary, dissolving them with heating.
- the solution can be filtered in order to separate undissolved constituents or impurities.
- the homogenization is carried out according to known methods with e.g. Rapid stirring, rotor-stator mills, dissolvers or similar devices.
- liquid preparations can be dried using known drying processes.
- the brightener preparations according to the invention are outstandingly suitable for the production of dyeing liquors for whitening polyacrylonitrile fibers by the exhaust process, preferably with a bleaching of the fiber material carried out in the same bath, for example with sodium chlorite.
- this preparation produces brilliant green tints.
- this preparation can achieve a 60-fold higher concentration.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Detergent Compositions (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Gegenstand der Erfindung sind Aufhellerpräparationen in fester oder flüssiger Form, die einen kationischen optischen Aufheller, ein anionisches Tensid und gegebenenfalls weitere Zusätze enthalten mit Ausnahme solcher Präparationen, die durch Schmelzformierung gewonnen werden.The invention relates to brightener preparations in solid or liquid form which contain a cationic optical brightener, an anionic surfactant and optionally other additives, with the exception of those preparations which are obtained by melt formation.
Aus FR-A-2 243 994 (entspricht DE-A 2 442 423) sind nämlich bereits staubfreie, gut rieselfähige Präparationen von optischen Aufhellern bekannt, die man durch eben diese Schmelzformierung von an sich beliebigen Aufhellern in Gegenwart von Trägermaterialien und gegebenenfalls einem Tensid erhält. Obwohl dor neben anionischen und nichtionischen Aufhellern auch kationische Typen beschrieben werden und als Tenside auch anionische Verbindungen genannt werden, fehlt jeglicher konkrete Hinweis, gerade die erfindungsgemäße Kombination von Aufhellerwirkstoff und Tensidart zu wählen.From FR-A-2 243 994 (corresponds to DE-A 2 442 423), dust-free, free-flowing preparations of optical brighteners are already known, which are obtained by this melt formation of brighteners of any kind in the presence of carrier materials and optionally a surfactant . Although cationic types are also described in addition to anionic and nonionic brighteners and anionic compounds are also mentioned as surfactants, there is no concrete indication that it is precisely the combination of brightener active ingredient and type of surfactant according to the invention that is to be selected.
Im übrigen sind für das Gelingen der Schemelzformierung naturgemäß die Anwendung relativ hoher Temperaturen und der Einsatz großer Mengen Trägermaterial (bezogen auf die Wirkstoffmenge) erforderlich, so daß mit Zersetzungserscheinungen an Träger und Aufheller sowie mit starken Umweltbelastungen gerechnet werden muß.In addition, the use of relatively high temperatures and the use of large amounts of carrier material (based on the amount of active ingredient) are naturally necessary for the successful formation of the stool, so that decomposition phenomena on the carrier and brightener as well as severe environmental pollution must be expected.
Erfindungsgemäß einsetzbare kationische optische Aufheller sind in der Literatur in großer Zahl beschrieben. Bevorzugt sind solche der allgemeinen Formel
- X = Triazolyl-Rest
- Y = Cumarinyl- oder Benzofuranyl-Rest
- Z = am N-Atom quaternierter heteroaromatischer Rest
- An° = Anion
bedeutetCationic optical brighteners which can be used according to the invention are described in large numbers in the literature. Those of the general formula are preferred
- X = triazolyl residue
- Y = coumarinyl or benzofuranyl residue
- Z = heteroaromatic residue quaternized on the N atom
- An ° = anion
means
Innerhalb dieser Gruppe sind solche bevorzugt bei denen
- Z = Triazolylrest mit quartärem Stickstoffatom, beispielsweise
- X die obige Bedeutung hat,
- Z Imidazolylrest mit quartärem N-Atom, z.B.
- Z = triazolyl radical with a quaternary nitrogen atom, for example
- X has the above meaning
- Z imidazolyl radical with a quaternary N atom, for example
Als anionische Tenside kommen u.a. solche in Betracht, wie sie in der DE-A-2 257 945 beschrieben sind. Beispielhaft seien genannt:
- Sulfatierte Alkylenoxidaddukte, sulfatierte partiell veresterte mehrwertige Alkohole, Alkylsulfonat, Natriumdialkylsulfosuccinate, Alkylbenzolsulfonate, Kondensationsprodukte aus Naphthalinsulfonsäuren oder Ditolylethersulfonäuren mit Formaldehyd, Ligninsulfonate und Oxyligninsulfonate, oder Kondensationsprodukte aus Kresol, 2-Napthol-6-sulfonsäure, Formaldehyd und Schwefelsäure: Bevorzugt sind Tenside mit Dispergiermitteleigenschaften, wie die vorstehend genannten Ligninderivate und Formaldehydkondensationsprodukte.
- Sulfated alkylene oxide adducts, sulfated partially esterified polyhydric alcohols, alkyl sulfonate, sodium dialkyl sulfosuccinates, alkyl benzene sulfonates, condensation products from naphthalenesulfonic acids or ditolyl ether sulfonic acids with formaldehyde, ligninsulfonates and oxyligninsulfonates, or condensation products from cresol, 2-naphthol-6-sulfonic acid, formaldehyde and sulfuric acid: surfactants with dispersant properties, such as the above-mentioned lignin derivatives and formaldehyde condensation products, are preferred.
Die anionischen Tenside können in Form de freien Säure oder in Form ihrer wasserlöslichen Salze eingesetzt werden.The anionic surfactants can be used in the form of the free acid or in the form of their water-soluble salts.
Weitere übliche Zusätze sind beispielsweise: anorganische Salze, wie NaCI, Na2S04; Salze organischer Säuren, z.B. CH3COONa, oder gut wasserlösliche organische Verbindungen, wie z.B. s-Caprolactam, Zucker, u.a.Other common additives are, for example: inorganic salts, such as NaCl, Na 2 S0 4 ; Salts of organic acids, for example CH 3 COONa, or readily water-soluble organic compounds, such as, for example, s-caprolactam, sugar, etc.
Die Konzentration des kationischen optischen Aufhellers in der vorzugsweise flüssigen wässrigen Präparation liegt im Bereich von 1-10%, die der anionischen Tenside von 3―40% und die der weiteren Zusätze ebenfalls von 3-40%.The concentration of the cationic optical brightener in the preferably liquid aqueous preparation is in the range from 1-10%, that of the anionic surfactants from 3―40% and that of the further additives likewise from 3-40%.
Die Herstellung der erfindungsgemäßen Aufhellerpräparationen erfolgt dadurch, daß die kationischen optischen Aufheller zusammen mit den anionischen Tensiden und ggf. den weiteren Zusätzen in wäßrigem Medium homogenisiert und ggf. unter Erwärmung in Lösung gebracht werden.The brightener preparations according to the invention are produced by homogenizing the cationic optical brighteners together with the anionic surfactants and possibly the other additives in an aqueous medium and, if necessary, dissolving them with heating.
Die Lösung kann ggf. filtriert werden, um noch ungelöste Bestandteile oder Verunreinigungen abzutrennen. Die Homogenisierung erfolgt nach bekannten Verfahren mit z.B. Schnellrühren, Rotor-Stator-Mühlen, Dissolvern oder ähnlichen Geräten.If necessary, the solution can be filtered in order to separate undissolved constituents or impurities. The homogenization is carried out according to known methods with e.g. Rapid stirring, rotor-stator mills, dissolvers or similar devices.
Wird eine fest Präparation gewünscht, so können die flüssigen Präparationen mit bekannten Trocknungsverfahren getrocknet werden.If a solid preparation is desired, the liquid preparations can be dried using known drying processes.
Die erfindungsgemäßen Aufhellerpräparate eignen sich hervorragend zur Herstellung von Färbeflotten zum Weißtönen von Polyacrylnitrilfasern nach dem Ausziehverfahren, vorzugsweise mit einer im selben Bad durchgeführten Bleiche des Fasermaterials, beispielsweise mit Natriumchlorit.The brightener preparations according to the invention are outstandingly suitable for the production of dyeing liquors for whitening polyacrylonitrile fibers by the exhaust process, preferably with a bleaching of the fiber material carried out in the same bath, for example with sodium chlorite.
3,6 g des optischen Aufhellers der Formel
Gegenüber der geringen Wasserlöslichkeit des Aufheller wirkstoffs von nur 0,07% kann mit der o.g. Zubereitung eine 50-fach höhere Konzentration erzielt werden.Compared to the low water solubility of the brightener active ingredient of only 0.07%, the above Preparation a concentration 50 times higher can be achieved.
7 g des Aufhellers aus Beispiel 1 werden mit 88 g des anionischen Tensids aus Beispiel 1 und 1 g CH3COONa in 250 g Wasser gelöst und anschließend zu einem Pulver mit 4 % Restfeuchte sprühgetrocknet.7 g of the brightener from example 1 are dissolved in 250 g of water with 88 g of the anionic surfactant from example 1 and 1 g of CH 3 COONa and then spray-dried to a powder with 4% residual moisture.
Diese Präparation ergibt auf Polyacrylnitrilfasern im Konzentrationsbereich von 0,2-2% und in Flottenverhältnissen von 1:10 bis 1:40 angewendet, brillante grünstichige Aufhellungen.Applied to polyacrylonitrile fibers in the concentration range of 0.2-2% and in liquor ratios of 1:10 to 1:40, this preparation produces brilliant green tints.
6 g des optischen Aufhellers der Formel
30 g dieses Pulvers werden in 70 g kockendem Wasser von pH 4 (essigsauer) gelöst. Diese Lösung bleibt auch nach dem Abkühlen auf Raumtemperatur erhalten.30 g of this powder are dissolved in 70 g of boiling water of pH 4 (acetic acid). This solution is retained even after cooling to room temperature.
Gegenüber der geringen Wasserlöslichkeit des Aufhellerwirkstoffs von nur 0,030% in Wasser kann mit dieser Präparation eine 60-fach höhere Konzentrtion erreicht werden.Compared to the low water solubility of the brightening agent of only 0.030% in water, this preparation can achieve a 60-fold higher concentration.
Die o.g. Präparation ergibt Polyacrynitrilfasern im Konzentrationsbereich von 0,2-2% und in Flottenverhältnissen von 1:10 bis 1:40 angewendet, brillante blaustichige Färbungen.The above Preparation results in polyacrynitrile fibers in the concentration range of 0.2-2% and in liquor ratios of 1:10 to 1:40, brilliant bluish tints.
Ähnliche Effekte erhält man, wenn man den in der vorstehend beschriebenen Präparation enthaltenen Aufheller durch den Aufheller gemäß Beispiel 1 ersetzt.Similar effects are obtained if the brightener contained in the preparation described above is replaced by the brightener according to Example 1.
Claims (3)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19813136809 DE3136809A1 (en) | 1981-09-16 | 1981-09-16 | OPTICAL BRIGHTNING PREPARATIONS |
DE3136809 | 1981-09-16 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0074590A2 EP0074590A2 (en) | 1983-03-23 |
EP0074590A3 EP0074590A3 (en) | 1984-05-16 |
EP0074590B1 true EP0074590B1 (en) | 1987-05-27 |
Family
ID=6141843
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP82108168A Expired EP0074590B1 (en) | 1981-09-16 | 1982-09-04 | Preparations of optical brighteners |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0074590B1 (en) |
JP (1) | JPS5861196A (en) |
DE (2) | DE3136809A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0498288U (en) * | 1991-01-22 | 1992-08-25 | ||
ES2225833T3 (en) * | 1994-05-12 | 2005-03-16 | Ciba Specialty Chemicals Holding Inc. | TEXTILE TREATMENT |
GB9413270D0 (en) * | 1994-07-01 | 1994-08-24 | Ciba Geigy Ag | Textile treatment |
GB9409465D0 (en) * | 1994-05-12 | 1994-06-29 | Ciba Geigy Ag | Protective use |
DE19500195A1 (en) * | 1995-01-05 | 1996-07-11 | Bayer Ag | Use of white-tinted plastics for tinting paper coating slips and such white-tinted paper coating slips |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1248652A (en) * | 1968-04-25 | 1971-10-06 | Du Pont | Water-insoluble dye salts |
DE2257945A1 (en) * | 1972-11-25 | 1974-05-30 | Basf Ag | Liquid and powdered cationic dyestuff prepns. - contg. excess anionic dispersants for dyeing/printing polyacrylonitrile, acid-modified polyesters and polyamides |
CH597335A5 (en) * | 1973-09-14 | 1978-03-31 | Ciba Geigy Ag |
-
1981
- 1981-09-16 DE DE19813136809 patent/DE3136809A1/en not_active Withdrawn
-
1982
- 1982-09-04 EP EP82108168A patent/EP0074590B1/en not_active Expired
- 1982-09-04 DE DE8282108168T patent/DE3276440D1/en not_active Expired
- 1982-09-13 JP JP57158246A patent/JPS5861196A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
EP0074590A2 (en) | 1983-03-23 |
DE3136809A1 (en) | 1983-03-31 |
JPS5861196A (en) | 1983-04-12 |
DE3276440D1 (en) | 1987-07-02 |
EP0074590A3 (en) | 1984-05-16 |
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