EP0495176A2 - Lessive en poudre - Google Patents

Lessive en poudre Download PDF

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Publication number
EP0495176A2
EP0495176A2 EP91119602A EP91119602A EP0495176A2 EP 0495176 A2 EP0495176 A2 EP 0495176A2 EP 91119602 A EP91119602 A EP 91119602A EP 91119602 A EP91119602 A EP 91119602A EP 0495176 A2 EP0495176 A2 EP 0495176A2
Authority
EP
European Patent Office
Prior art keywords
alkyl
fatty alcohol
mixtures
carbon atoms
powder detergent
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
EP91119602A
Other languages
German (de)
English (en)
Other versions
EP0495176A3 (en
EP0495176B1 (fr
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.)
Sasol Germany GmbH
Original Assignee
Huels AG
Chemische Werke Huels 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=6423098&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0495176(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Huels AG, Chemische Werke Huels AG filed Critical Huels AG
Publication of EP0495176A2 publication Critical patent/EP0495176A2/fr
Publication of EP0495176A3 publication Critical patent/EP0495176A3/de
Application granted granted Critical
Publication of EP0495176B1 publication Critical patent/EP0495176B1/fr
Anticipated expiration legal-status Critical
Revoked legal-status Critical Current

Links

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
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • 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
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • C11D10/045Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap based on non-ionic surface-active compounds and soap
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/14Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/22Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/662Carbohydrates or derivatives
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

Definitions

  • the present invention relates to powdered preparations for washing textiles, the surfactants of which are largely produced from renewable raw materials.
  • Powder detergents produced either by spray drying or agglomeration processes, today consist of surfactants, builders, bleaches and additives in smaller quantities such as optical brighteners, graying inhibitors, corrosion inhibitors, foam regulators, stabilizers, possibly odorants, dyes etc.
  • the surfactant component is usually in the foreground, usually a combination of anionic and nonionic surfactants, the essential basis of which is petroleum today.
  • the object of the invention was therefore to find a surfactant combination for powdered detergents which are largely made from renewable raw materials and which are extremely biodegradable, these powders having to achieve very good washing results.
  • This object was achieved by a surfactant combination consisting of alkyl polyglycosides with a degree of glycosidation ⁇ 1.4 as well as fatty alcohol oxyethylates, anionic surfactants and soap.
  • alkyl polyglycosides in combination with fatty alcohol oxyethylates, in the presence of anionic surfactants in small amounts, achieve very good washing results in the powder mixtures according to the invention.
  • alkyl polyglycoside in combination with anionic and nonionic surfactants is described in European applications EP-0 075 994, EP-0 075 995 and EP-0 075 996; here the degree of glycosidation is G ⁇ 1.5.
  • Alkyl polyglucosides are particularly preferred.
  • the alkyl polyglycosides used according to the invention can be produced by known processes based on renewable raw materials.
  • dextrose is reacted with n-butanol to give butylpolyglycoside mixtures in the presence of an acidic catalyst, which are transglycosidated with long-chain alcohols in the presence of an acidic catalyst to give the desired alkylpolyglycoside mixtures.
  • dextrose is immediately reacted with the desired long-chain alcohol.
  • the structure of the products can be varied within certain limits.
  • the alkyl radical R is determined by the choice of the long-chain alcohol.
  • the industrially accessible alcohols with 8 to 18 carbon atoms, in particular native alcohols from the hydrogenation of carboxylic acids or carboxylic acid derivatives.
  • Ziegler alcohols or oxo alcohols can also be used.
  • the polyglycosyl radicals Z n are determined, on the one hand, by the selection of the carbohydrate and, on the other hand, by setting the average degree of polymerization n z. B. according to DE-OS 19 43 689.
  • polysaccharides e.g. B. starch, maltodextrins, dextrose, galactose, mannose, xylose, etc.
  • the industrially available carbohydrates starch, maltodextrins and especially dextrose are preferred.
  • Alkyl polyglycosides used according to the invention can also be prepared by mixing alkyl polyglycosides with alkyl monoglycosides.
  • the latter can e.g. B. according to EP-A 0 092 355 using polar solvents, such as acetone, from alkyl polyglycosides.
  • the degree of glycosidation is advantageously determined by means of 1 H-NMR.
  • the detergents according to the invention contain 2 to 18% alkyl polyglycoside, preferably 3 to 15%.
  • the alkyl polyglycosides are considered to be extremely environmentally compatible.
  • the degree of biodegradation for the alkyl polyglycosides according to the invention determined by means of a sewage treatment plant simulation model / DOC analysis, is 96 ⁇ 3%. This figure can be seen against the background that with this test method (total degradation) a degree of degradation ⁇ 70% already indicates the substance to be readily degradable.
  • the acute oral toxicity LD 50 (rat) with> 10,000 mg / kg as well as the aquatic toxicity LC 50 (gold orfe) with approx. 12 mg / l and EC 50 (daphnia) with 30 mg / l are by a factor of 3 to 5 cheaper than the corresponding values of today's most important surfactants. The same applies to skin and mucous membrane compatibility.
  • the compounds are generally made by addition of ethylene oxide onto longer-chain alcohols in the presence of basic or acidic Catalysts made.
  • basic or acidic Catalysts made.
  • commercially available alcohols with 8 to 22 carbon atoms from the hydrogenation of carboxylic acids or carboxylic acid derivatives are favorable.
  • Ziegler alcohols or oxo alcohols can also be used.
  • the alcohol oxyethylates are known to be readily biodegradable; Their data are also favorable with regard to aquatoxicity, skin and mucous membrane compatibility.
  • the liquid detergents according to the invention contain 2 to 18% fatty alcohol oxyethylates, which can also be mixtures. Contents of 3 to 15% by weight are preferred.
  • Anionic surfactants :
  • Anionic surfactants used are alkylbenzene sulfate, alkane sulfonates, olefin sulfonates, fatty alcohol sulfates and fatty alcohol ether sulfates or their mixtures having 9 to 20 carbon atoms in the alkyl or alkylene group. Na, K, NH4, Mg and their mixtures are the counterions. These anionic surfactants, which can be present in the mixtures according to the invention in amounts of 0 to 12% by weight, are not to be understood as soap. Amounts of 1 to 10% by weight are preferred.
  • Fatty acid salts or their acids according to the invention correspond to formula III R '''COOP III, in which R '''is a saturated or unsaturated alkyl radical having 8 to 22 carbon atoms and P is hydrogen, alkali, ammonium or alkanolammonium.
  • the detergents according to the invention contain 0.5 to 30% soap, which will usually be a mixture of different components. Contents of 1 to 25% are preferred.
  • builders should be mentioned as non-surfactant components.
  • water-soluble builders such as different polyphosphates, phosphonates, carbonates, polycarboxylates, citronates, polyacetates such as NTA and EDTA etc. or mixtures thereof are used. These compounds are usually used as alkali salts, preferably as sodium salts. Although not complexing, sodium sulfate should also be mentioned here.
  • water-insoluble builders such as aluminosilicates of suitable particle size, is also according to the invention (cf. EP-A 0 075 994).
  • the concentration of the builders in the detergent is 0 to 70%, preferably 0 to 50%.
  • Bleaching agents such as sodium perborate, optionally combined with bleach activators such as tetraacetylethylene diamine etc. or percarbonate, are also used according to the invention; Other bleaching agents are of course also possible (cf. K. Engel, Tenside Surfactants 25, S. (1988).
  • concentration of the bleaching agents is 0 to 40%, preferably 0-30%.
  • Adjusting agents such as low molecular weight mono- or dihydric alcohols, alkyl ethers of polyhydric alcohols, hydrotropics such as alkylbenzenesulfonates with 1 to 3 carbon atoms in the alkyl radical, alkanolamines or urea, enzymes such as in particular proteases and enzyme stabilizers, corrosion inhibitors such as alkali silicates, optical, may be used according to the invention
  • the total use concentration in the powder detergents according to the invention is 0.1-10 g / l for the surfactant fraction according to the invention. 0.2 - 7 g / l are preferred.
  • the application concentration of the washing powder according to the invention is 1-20 g / l.
  • washing powders listed in Table 1 contain in addition to the above-mentioned surfactant components used according to the invention each 11% sodium perborate, 1.7% sodium metasilicate, 2.5% magnesium silicate, 14% Na2SO4, 3% Sokalan R CP 5, 9% soda, 23% Wesslith R P, 4% TAED R and 0.5% Sequion R 10 NA 2.
  • the washing powders listed in Table 2 contain 11% sodium perborate, 1.7% sodium metasilicate, 2.5% magnesium silicate, 14% Na2SO4, 14.5% Na5P3O10, 4% soda, 14% Wesslith R P, 3% TAED R , 0.5% Sequion R 10 NA 2 and 1% Na3PO4.
  • the liquid components were added to the mixture of solid components in small portions with intensive stirring. Stirring ensures sample homogeneity.
  • the known methods were used to characterize the powders in terms of bulk density and angle of repose.
  • the washability was determined in a normal household washing machine, and the foam development was also checked.

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)
EP91119602A 1991-01-16 1991-11-16 Lessive en poudre Revoked EP0495176B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4101070 1991-01-16
DE4101070A DE4101070A1 (de) 1991-01-16 1991-01-16 Waschpulver

Publications (3)

Publication Number Publication Date
EP0495176A2 true EP0495176A2 (fr) 1992-07-22
EP0495176A3 EP0495176A3 (en) 1992-10-14
EP0495176B1 EP0495176B1 (fr) 1995-06-21

Family

ID=6423098

Family Applications (1)

Application Number Title Priority Date Filing Date
EP91119602A Revoked EP0495176B1 (fr) 1991-01-16 1991-11-16 Lessive en poudre

Country Status (6)

Country Link
EP (1) EP0495176B1 (fr)
AT (1) ATE124080T1 (fr)
DE (2) DE4101070A1 (fr)
DK (1) DK0495176T3 (fr)
ES (1) ES2074204T3 (fr)
NO (1) NO920186L (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999043774A1 (fr) * 1998-02-26 1999-09-02 Henkel Kommanditgesellschaft Auf Aktien Detergent et nettoyant pulverulent a granulaire
WO2011047950A1 (fr) 2009-10-20 2011-04-28 Unilever Plc Améliorations de compositions de blanchisserie
WO2011047951A1 (fr) 2009-10-20 2011-04-28 Unilever Plc Compositions de blanchisserie

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE60309741T2 (de) 2002-12-03 2007-03-29 Unilever N.V. Behandlungszusammensetzungen für wäsche

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0075995A2 (fr) * 1981-09-28 1983-04-06 THE PROCTER & GAMBLE COMPANY Compositions détergentes contenant de mélanges d'alcylpolysaccharide et d'agents tensio-actifs non-ioniques
US4536319A (en) * 1983-10-04 1985-08-20 The Procter & Gamble Company Compositions comprising alkylpolysaccharide detergent surfactant

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4029035A1 (de) * 1990-09-13 1992-03-19 Huels Chemische Werke Ag Waschmittel

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0075995A2 (fr) * 1981-09-28 1983-04-06 THE PROCTER & GAMBLE COMPANY Compositions détergentes contenant de mélanges d'alcylpolysaccharide et d'agents tensio-actifs non-ioniques
US4536319A (en) * 1983-10-04 1985-08-20 The Procter & Gamble Company Compositions comprising alkylpolysaccharide detergent surfactant

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999043774A1 (fr) * 1998-02-26 1999-09-02 Henkel Kommanditgesellschaft Auf Aktien Detergent et nettoyant pulverulent a granulaire
WO2011047950A1 (fr) 2009-10-20 2011-04-28 Unilever Plc Améliorations de compositions de blanchisserie
WO2011047951A1 (fr) 2009-10-20 2011-04-28 Unilever Plc Compositions de blanchisserie

Also Published As

Publication number Publication date
DE59105791D1 (de) 1995-07-27
EP0495176A3 (en) 1992-10-14
DE4101070A1 (de) 1992-07-23
NO920186D0 (no) 1992-01-15
ATE124080T1 (de) 1995-07-15
DK0495176T3 (da) 1995-10-02
EP0495176B1 (fr) 1995-06-21
ES2074204T3 (es) 1995-09-01
NO920186L (no) 1992-07-17

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