EP0376893A2 - Flüssiges Wäschewaschmittel, enthaltend optische Aufheller - Google Patents

Flüssiges Wäschewaschmittel, enthaltend optische Aufheller Download PDF

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Publication number
EP0376893A2
EP0376893A2 EP89810985A EP89810985A EP0376893A2 EP 0376893 A2 EP0376893 A2 EP 0376893A2 EP 89810985 A EP89810985 A EP 89810985A EP 89810985 A EP89810985 A EP 89810985A EP 0376893 A2 EP0376893 A2 EP 0376893A2
Authority
EP
European Patent Office
Prior art keywords
laundry detergent
liquid laundry
detergent composition
formula
composition 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.)
Withdrawn
Application number
EP89810985A
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English (en)
French (fr)
Other versions
EP0376893A3 (de
Inventor
Jean-Pierre Chavannes
Rolf-Heinz Forrer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sandoz AG
Original Assignee
Sandoz AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sandoz AG filed Critical Sandoz AG
Publication of EP0376893A2 publication Critical patent/EP0376893A2/de
Publication of EP0376893A3 publication Critical patent/EP0376893A3/de
Withdrawn legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/40Dyes ; Pigments
    • C11D3/42Brightening agents ; Blueing agents

Definitions

  • the invention relates to liquid laundry detergent compositions containing optical brighteners.
  • optical brighteners in laundry detergent compositions has been known for a long time.
  • op­tical brighteners with poor water solubility are used as dispersions because such products should have enough substantivity, which means that their affinity to the fibres of the substrate that is to be washed, should be high enough in order not to be washed out immediately.
  • the use of such products has the disadvantage that the detergent compositions have a poor storage stability, that is to say that the optical brightener will precipitate. If, on the other hand, optical brighteners were to be used which are more soluble in water, these products would have an insufficient substantivity to the fibres of the substrate to be washed.
  • both groups R are the same and both groups X are the same and the alkyl and alkylene groups have the same number of carbon atoms i.e. compounds of formulae I and II are preferably symmetrical. More preferably, in compounds of formula 1, X is other than hydroxy or R1 is hydrogen. Especially preferred compounds have the structure of formulae III, IV, V, VI and/or VII. Most preferred compound is the one of formula III.
  • optical brighteners according to the invention are used in powder form or as solutions in water. Such solutions have a content of 18 to 75% by weight of active substance and preferably also contain hydrotropic substances.
  • active substances are well known and can be produced according to conventional processes.
  • liquid laundry detergent compositions according to the invention contain the usual components of such compositions.
  • such components include anionic as well as non-ionic surfactants, builders, alkali, hydrotropic agents, buffers, enzymes and the like will be contained. It is also possible to include cationic softeners which will not precipitate.
  • Typical detergent compositions contain from 0.05 to 0.15% by weight of optical brighteners (as 100% active substance), from 5 to 30%, preferably from 10 to 25% by weight of fatty acids, from 2 to 20%, preferably from 5 to 15% by weight of a further anionic surfactant, from 0.5 to 12%, preferably from 1.5 to 8% by weight of a non-ionic surfactant, to give in total from 20 to 50%, preferably from 30 to 50% by weight of surfactants and from 5 to 15% by weight of builders.
  • the amount of alkali should be sufficient to neutralize all acids present and to reach a pH value suitable for washing.
  • the fatty acids which are used as anionic surfactants are preferably saturated and unsaturated C5 ⁇ 22 carboxylic acids, more preferably C12 ⁇ 18.
  • the fatty acids for example coco fatty acid or oleic acid are added as such and converted to the salt form by addition of alkali e.g. NaOH, KOH or an organic base e.g. triethanolamine.
  • anionic surfactants which can be present may be any of the following conventional types:
  • a preferred class of surfactants which are only weakly anionic are of the formula IX R-O-(CH2CH2O (A-COOH) x IX in which R is the residue of a C8 ⁇ 22 fatty alcohol or of an alkylphenol having 10-24 C atoms; A is a methylene or ethylene group; m is a number from 1-20; and x is an average value from 0.1 to 1.
  • the most preferred component (B) is a compound of formula IX obtained by reacting a synthetic lauryl alcohol (C12 ⁇ 15) with 4-5 moles ethylene oxide and subsequently with 0.8 mole chloracetic acid.
  • the compounds are normally used in the form of their alkali metal salts, particularly sodium salts.
  • Nonionic surfactants which may be present include ethylene oxide (EO) / propylene oxide (PO) block copolymers (Pluronics), and the addition products of EO or PO, preferably EO, to fatty alcohols, fatty amines, fatty acids, fatty acid alkanolamides and alkylphenols. Such non-ionic surfactants are conventional and commercially available.
  • Hydrotropic compounds which may be present include for example urea, dicyandiamide and its derivatives, alcohols, water-soluble glycols, glycol ethers and glycol esters and C1 ⁇ 4 alkylbenzene­sulphonates, provided that the compounds display no cloud point in distilled water up to 100°. They act so as to prevent phase separ­ation, that is to stabilize the liquid composition.
  • Sequestering agents include citric acid, nitrilotriacetic acid and other complex formers. Buffers may be used to stabilise the pH of the wash liquor in the neutral or alkali region. Buffer substances include sodium bicarbonate, sodium carbonate and sodium silicate.
  • cationic softeners e.g., products of acylation and quaternization of a polyalkylene polyamine of the formula X in which each R1, independently, is C12 ⁇ 18 alkyl or C12 ⁇ 18 alkenyl; each n, independently, is 2 or 3; R2 is C1 ⁇ 4 alkyl, C1 ⁇ 4 hydroxyalkyl, or C1 ⁇ 4 hydroxyalkyl etherified with 1-10 ethylene oxide groups; R3 is C1 ⁇ 4 alkyl or benzyl; and X ⁇ is a halide, methylsulphate or ethylsulphate anion.
  • cationic softeners e.g., products of acylation and quaternization of a polyalkylene polyamine of the formula X in which each R1, independently, is C12 ⁇ 18 alkyl or C12 ⁇ 18 alkenyl; each n, independently, is 2 or 3; R2 is C1 ⁇ 4 alkyl, C1 ⁇ 4 hydroxyalkyl,
  • the liquid detergent compositions of the invention are primarily useful as domestic laundry detergents. Not only do they display good washing power, they also produce a soft handle on laundered cotton goods. Being phosphate-free, they are ecologically acceptable.
  • the liquid compositions of the invention are stable and do not separate into two phases, nor do the optical brighteners crystallize and precipitate on storage.
  • the carboxymethylated ethylene oxide adduct of the formula C12 ⁇ 15O(CH2CH2O) 4,5 - (CH2COONa) 0,7 as a 50% paste in water, the non-ionic surfactant of the formula as a 99% paste in water, the softener of the formula in which R x 85% oleic acid and 15% stearic acid residue, as a 90% solution in water, polyacrylic acid A with MW 100.00 as a solution of 29% of the semi-neutralized acid (sodium salt), polyacrylic acid B with MW 4500 as a solution of 49% are used as well as the optical brighteners with the given formulas in the following compositions: Formula III as an aqueous solution that contains 28% active substance or as a powder with 89% active substance Formula IV as an aqueous solution that contains 20% active substance Formula V as an aqueous solution that contains 23% active substance or as a powder with 50% active substance Formula VII as an aqueous
  • Example 1 is a so-called fabric softener
  • Example 2 is a liquid laundry detergent for industrial use
  • Example 3 is a complete laundry detergent for domestic use
  • Example 4 is a liquid laundry detergent with fabric softener for domestic use
  • Examples 5 and 6 are liquid laundry detergents for domestic use
  • Example 7 is a concentrated complete laundry detergent for domestic use.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)
EP19890810985 1988-12-30 1989-12-27 Flüssiges Wäschewaschmittel, enthaltend optische Aufheller Withdrawn EP0376893A3 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3844341 1988-12-30
DE19883844341 DE3844341A1 (de) 1988-12-30 1988-12-30 Fluessige waschmittel

Publications (2)

Publication Number Publication Date
EP0376893A2 true EP0376893A2 (de) 1990-07-04
EP0376893A3 EP0376893A3 (de) 1991-08-07

Family

ID=6370541

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19890810985 Withdrawn EP0376893A3 (de) 1988-12-30 1989-12-27 Flüssiges Wäschewaschmittel, enthaltend optische Aufheller

Country Status (3)

Country Link
EP (1) EP0376893A3 (de)
JP (1) JPH02227497A (de)
DE (1) DE3844341A1 (de)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5873913A (en) * 1994-06-23 1999-02-23 Clariant Finance (Bvi) Limited Optical brightening agents
EP1752453A1 (de) 2005-08-04 2007-02-14 Clariant International Ltd. Lagerstabile Lösungen von optischen Aufhellern
CN113574160A (zh) * 2019-03-19 2021-10-29 宝洁公司 洗涤织物的方法
US11878077B2 (en) 2019-03-19 2024-01-23 The Procter & Gamble Company Fibrous water-soluble unit dose articles comprising water-soluble fibrous structures

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS483889U (de) * 1971-05-26 1973-01-17
JPS515412B1 (de) * 1970-09-28 1976-02-19
FR2378119A1 (fr) * 1977-01-22 1978-08-18 Hoechst Ag Compositions liquides d'azureurs optiques renfermant des produits d'alcoxylation
US4233167A (en) * 1979-06-14 1980-11-11 S. C. Johnson & Son, Inc. Liquid detergent softening and brightening composition
SU804678A1 (ru) * 1978-06-19 1981-02-15 Предприятие П/Я М-5400 Жидкий препарат оптическогоОТбЕлиВАТЕл
DD230531A3 (de) * 1983-07-21 1985-12-04 Bitterfeld Chemie Verfahren zur herstellung eines optischen aufhellungsmittels der bistriazinylaminostilben-reihe
EP0275694A1 (de) * 1986-12-24 1988-07-27 Unilever Plc Flüssiger Gewebeweichmacher
GB2204609A (en) * 1987-05-11 1988-11-16 Sandoz Ltd Liquid detergent/softener compositions

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1234486A (de) * 1968-07-20 1971-06-03
GB1281189A (en) * 1969-12-20 1972-07-12 Ciab Geigy U K Ltd Method of whitening triazine-type optical bleaching agents
JPS591598A (ja) * 1982-06-25 1984-01-06 花王株式会社 洗浄剤組成物

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS515412B1 (de) * 1970-09-28 1976-02-19
JPS483889U (de) * 1971-05-26 1973-01-17
FR2378119A1 (fr) * 1977-01-22 1978-08-18 Hoechst Ag Compositions liquides d'azureurs optiques renfermant des produits d'alcoxylation
SU804678A1 (ru) * 1978-06-19 1981-02-15 Предприятие П/Я М-5400 Жидкий препарат оптическогоОТбЕлиВАТЕл
US4233167A (en) * 1979-06-14 1980-11-11 S. C. Johnson & Son, Inc. Liquid detergent softening and brightening composition
DD230531A3 (de) * 1983-07-21 1985-12-04 Bitterfeld Chemie Verfahren zur herstellung eines optischen aufhellungsmittels der bistriazinylaminostilben-reihe
EP0275694A1 (de) * 1986-12-24 1988-07-27 Unilever Plc Flüssiger Gewebeweichmacher
GB2204609A (en) * 1987-05-11 1988-11-16 Sandoz Ltd Liquid detergent/softener compositions

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, vol. 110, no. 22, 29 May 1989 Columbus, Ohio, USA page 128; right-hand column; ref. no. 195198R *
CHEMICAL ABSTRACTS, vol. 79, no. 22, 3 December 1973 Columbus, Ohio, USA page 59; left-hand column; ref. no. 127576D & JP-U-48 003 889 (SUMITOMO CHEMICAL CO., LTD.) *
CHEMICAL ABSTRACTS, vol. 85, no. 12, 20 September 1976 Columbus, Ohio, USA page 129; right-hand column; ref. no. 80081 & JP-A-51 005 412 (SHINNICHI SOKAKO CO.,LTD.) *
CHEMICAL ABSTRACTS, vol. 95, no. 6, 10 August 1981 Columbus, Ohio, USA page 72; right-hand column; ref. no. 44673N & SU-A-804678 (A.I. BUKHANKO ET AL.) *
JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY. vol. 65, no. 4, April 1988, CHAMPAIGN US pages 679 - 683; W.R. FINDLEY: "FLUORESCENT WHITENING AGENTS FOR MODERN DETERGENTS" *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5873913A (en) * 1994-06-23 1999-02-23 Clariant Finance (Bvi) Limited Optical brightening agents
EP1752453A1 (de) 2005-08-04 2007-02-14 Clariant International Ltd. Lagerstabile Lösungen von optischen Aufhellern
US8221588B2 (en) 2005-08-04 2012-07-17 Clariant Finance (Bvi) Limited Storage stable solutions of optical brighteners
CN113574160A (zh) * 2019-03-19 2021-10-29 宝洁公司 洗涤织物的方法
US11878077B2 (en) 2019-03-19 2024-01-23 The Procter & Gamble Company Fibrous water-soluble unit dose articles comprising water-soluble fibrous structures

Also Published As

Publication number Publication date
JPH02227497A (ja) 1990-09-10
EP0376893A3 (de) 1991-08-07
DE3844341A1 (de) 1990-07-05

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