EP0622448A2 - Détergent - Google Patents

Détergent Download PDF

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Publication number
EP0622448A2
EP0622448A2 EP94104556A EP94104556A EP0622448A2 EP 0622448 A2 EP0622448 A2 EP 0622448A2 EP 94104556 A EP94104556 A EP 94104556A EP 94104556 A EP94104556 A EP 94104556A EP 0622448 A2 EP0622448 A2 EP 0622448A2
Authority
EP
European Patent Office
Prior art keywords
acid
weight
washing
detergent
wfk
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.)
Granted
Application number
EP94104556A
Other languages
German (de)
English (en)
Other versions
EP0622448B1 (fr
EP0622448A3 (fr
Inventor
Franz-Josef Dr. Dany
Werner Gohla
Ernst Ingo Dr. Leupold
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.)
Clariant Produkte Deutschland GmbH
Original Assignee
Hoechst 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 Hoechst AG filed Critical Hoechst AG
Publication of EP0622448A2 publication Critical patent/EP0622448A2/fr
Publication of EP0622448A3 publication Critical patent/EP0622448A3/fr
Application granted granted Critical
Publication of EP0622448B1 publication Critical patent/EP0622448B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/12Water-insoluble compounds
    • C11D3/124Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246Silicates, e.g. diatomaceous earth
    • C11D3/128Aluminium silicates, e.g. zeolites
    • 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
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/12Water-insoluble compounds
    • C11D3/124Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246Silicates, e.g. diatomaceous earth
    • C11D3/1253Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite
    • C11D3/1273Crystalline layered silicates of type NaMeSixO2x+1YH2O
    • 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
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds

Definitions

  • the invention relates to a detergent with 5 to 50% by weight, preferably 10 to 30% by weight, at least one surfactant, 0.5 to 60% by weight, preferably 5 to 60% by weight, builders and customary washing auxiliaries.
  • silicate detergent builders so-called builders, e.g. Zeolite A and / or crystalline layered sodium silicate in combination with organic polycarboxylic acids, e.g. Citric acid or its salts is known from EP-0 405 122 A2. It is desirable that such polycarboxylic acids increase the washing performance of the detergents provided with them and are largely harmless from an ecological point of view, i.e. are readily biodegradable. This requirement also includes a pronounced lime binding capacity that should be preserved as far as possible over a temperature range of 20 to 90 ° C, as is common in household laundry.
  • polyglycol diacid (CAS No. 39927-08-7) fulfills these requirements in the broadest sense.
  • the lime binding capacity of polyglycol diacid is 220 mg Ca / g, at 60 and 90 ° C it is still 80 mg Ca / g, while citric acid only contains lime binders of 195 mg Ca / g at room temperature and 30 mg Ca / g at 90 ° C owns.
  • the detergent of the invention is now characterized in that it contains 3 to 11% by weight of polyglycol diacid in addition to other builders.
  • Detergent formulations which, in addition to crystalline layered sodium silicate and / or zeolite A, contain polyglycol diacid in concentrations of 3 to 10% by weight, mostly provide very good washing performance both with regard to dirt removal and with regard to preventing tissue deposits.
  • the detergents were produced by the spray mixing method.
  • a free-fall mixer was used in which the solid powdery components were premixed.
  • the liquid ingredients were then sprayed onto the dry premix. The procedure is described in detail in the magazine "Seifen, Fette, ⁇ le, Wwachs” 99 (1973), pp. 351-357.
  • test formulations given in Table 1 (Examples 1 to 12), including a commercial detergent, were tested under washing conditions in accordance with the following conditions:
  • Table 2 shows the washing results obtained with Examples 1-12.
  • the individual results which were measured on the test fabrics BW 101 (EMPA) and PE / BW 20C (WFK) are shown.
  • the secondary washing effect is shown in the form of the average ash values (average of 5 test fabrics).
  • Examples 2-4 and 8-11 according to the invention are superior in all respects to Comparative Examples 1 and 5 (without polyglycol diacid). But also in comparison with the commercial detergent concentrate No. 12, the examples 2-4 and 8-11 according to the invention show a clearly better washing performance.
  • Examples 6 and 7 represent borderline cases which show that zeolite A generally does not show the good washing action as SKS 6, which is why without SKS 6 more than 6% by weight polyglycol diacid should be present in the detergent.
  • Nonionic surfactants are understood to mean those compounds which have an organic, hydrophobic group and a hydrophilic radical, for example the condensation products of alkylphenols or higher fatty alcohols with ethylene oxide (fatty alcohol ethoxylates), the condensation products of polypropylene glycol with ethylene oxide or propylene oxide, the condensation products of Ethylene oxide with the reaction product of ethylenediamine and propylene oxide, as well as long-chain tertiary amine oxides
  • surfactants with a zwitterionic (ampholytic) character include the following compounds: Derivatives of aliphatic, secondary and tertiary amines or quaternary ammonium compounds with 8 to 18 carbon atoms and a hydrophilic group in the aliphatic radical, such as sodium 3-dodecylaminopropionate, sodium 3-dodecylaminopropanesulfonate, 3- (N, N-dimethyl-N -hexadec
  • Suitable washing auxiliaries according to the invention are weakly acidic, neutral or alkaline inorganic complexing agents.
  • Useful, weakly acidic, neutral or alkaline-reacting salts are, for example, the bicarbonates or carbonates of the alkalis, furthermore the alkali salts of organic, non-capillary-active sulfonic acids, carboxylic acids and sulfocarboxylic acids containing 1 to 8 carbon atoms.
  • water-soluble salts of benzene, toluene or xylene sulfonic acid water-soluble salts of sulfoacetic acid, sulfobenzoic acid or salts of sulfodicarboxylic acids as well as the salts of acetic acid, lactic acid, citric acid, tartaric acid, oxydiacetic acid (HOOC-CH2-O-CH2-COOH) acid, oxydib , 1,2,3,4-cyclopentanetetracarboxylic acid, polycarboxylates, polyacrylic acid and polymaleic acid.
  • acetic acid lactic acid, citric acid, tartaric acid, oxydiacetic acid (HOOC-CH2-O-CH2-COOH) acid, oxydib , 1,2,3,4-cyclopentanetetracarboxylic acid, polycarboxylates, polyacrylic acid and polymaleic acid.
  • the organic complexing agents include, for example, nitrilotriacetic acid, ethylenediaminetetraacetic acid, N-hydroxyethylethylenediaminetriacetic acid or polyalkylene-polyamine-N-polycarboxylic acids.
  • Washing aids according to the invention also include products such as the alkali or ammonium salts of sulfuric acid, boric acid, alkylene, hydroxyalkylene or aminoalkylenephosphonic acid, as well as bleaching agents, stabilizers for peroxide compounds (bleaching agents) and water-soluble organic complexing agents.
  • the bleaching agents include sodium perborate or tetrahydrate, sodium percarbonate, the alkali metal salts of peroxomono- or peroxodisulfuric acid, the alkali metal salts of peroxodiphosphoric acid (H4P2O8), and alkali metal salts of peroxocarboxylic acids, such as diperoxododecanedioic acid.
  • stabilizers for these bleaching agents are water-soluble, precipitated magnesium silicate, organic complexing agents such as the alkali salts of iminodiacetic acid, nitrilotriacetic acid, tetraacetylethylene diamine (TAED), methylene diphosphonic acid, 1-hydroxyethane-1,1-diphosphonic acid and nitrilotrismethylene phosphonic acid.
  • organic complexing agents such as the alkali salts of iminodiacetic acid, nitrilotriacetic acid, tetraacetylethylene diamine (TAED), methylene diphosphonic acid, 1-hydroxyethane-1,1-diphosphonic acid and nitrilotrismethylene phosphonic acid.
  • Washing aids that increase the dirt-carrying capacity of washing liquors, such as carboxymethyl cellulose, carboxymethyl starch, methyl cellulose or copolymers of maleic anhydride with methyl vinyl ether or acrylic acid, foam regulators, such as mono- and dialkyl phosphoric acid esters with 16 to 20 carbon atoms in the alkyl radical, and optical brighteners, disinfectants and enzymes, such as proteas , Amylases, lipases can also be additional components of the detergent of the invention.
  • foam regulators such as mono- and dialkyl phosphoric acid esters with 16 to 20 carbon atoms in the alkyl radical
  • optical brighteners disinfectants and enzymes, such as proteas , Amylases, lipases can also be additional components of the detergent of the invention.

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)
  • Inorganic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Detergent Compositions (AREA)
EP94104556A 1993-04-24 1994-03-23 Détergent Expired - Lifetime EP0622448B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4313529 1993-04-24
DE4313529A DE4313529A1 (de) 1993-04-24 1993-04-24 Waschmittel

Publications (3)

Publication Number Publication Date
EP0622448A2 true EP0622448A2 (fr) 1994-11-02
EP0622448A3 EP0622448A3 (fr) 1995-05-31
EP0622448B1 EP0622448B1 (fr) 1999-07-21

Family

ID=6486328

Family Applications (1)

Application Number Title Priority Date Filing Date
EP94104556A Expired - Lifetime EP0622448B1 (fr) 1993-04-24 1994-03-23 Détergent

Country Status (4)

Country Link
EP (1) EP0622448B1 (fr)
JP (1) JPH0748597A (fr)
DE (2) DE4313529A1 (fr)
ES (1) ES2135499T3 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995031526A1 (fr) * 1994-05-11 1995-11-23 The Procter & Gamble Company Compositions pour inhiber le transfert des couleurs, contenant des catalyseurs constitues de complexes metalliques speciaux
US5908821A (en) * 1994-05-11 1999-06-01 Procter & Gamble Company Dye transfer inhibiting compositions with specifically selected metallo catalysts

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0317193A (ja) * 1989-06-14 1991-01-25 Kawaken Fine Chem Co Ltd 硬質表面洗浄剤
JPH03170410A (ja) * 1989-11-29 1991-07-24 Kawaken Fine Chem Co Ltd 毛髪化粧料組成物
EP0480757A1 (fr) * 1990-10-12 1992-04-15 Tosoh Corporation Procédé pour évitér l'agglomération de poudre

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0317193A (ja) * 1989-06-14 1991-01-25 Kawaken Fine Chem Co Ltd 硬質表面洗浄剤
JPH03170410A (ja) * 1989-11-29 1991-07-24 Kawaken Fine Chem Co Ltd 毛髪化粧料組成物
EP0480757A1 (fr) * 1990-10-12 1992-04-15 Tosoh Corporation Procédé pour évitér l'agglomération de poudre

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, vol. 98, no. 14, 4. April 1983, Columbus, Ohio, US; abstract no. 109307e, Seite 109 ;Spalte R ; & CS-A-189 228 (HELL JIRI ET AL.) 1. August 1982 *
DATABASE WPI Week 9110, Derwent Publications Ltd., London, GB; AN 91-069133 & JP-A-3 017 193 (KAWA-KEN-FINE CHEM) 25. Januar 1991 *
DATABASE WPI Week 9136, Derwent Publications Ltd., London, GB; AN 91-262295 & JP-A-3 170 410 (KAWA-KEN-FINE CHEM K) 29. November 1989 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995031526A1 (fr) * 1994-05-11 1995-11-23 The Procter & Gamble Company Compositions pour inhiber le transfert des couleurs, contenant des catalyseurs constitues de complexes metalliques speciaux
US5908821A (en) * 1994-05-11 1999-06-01 Procter & Gamble Company Dye transfer inhibiting compositions with specifically selected metallo catalysts

Also Published As

Publication number Publication date
DE59408502D1 (de) 1999-08-26
ES2135499T3 (es) 1999-11-01
EP0622448B1 (fr) 1999-07-21
JPH0748597A (ja) 1995-02-21
DE4313529A1 (de) 1994-10-27
EP0622448A3 (fr) 1995-05-31

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