EP0373349A2 - Détergent liquide pour surfaces dures - Google Patents

Détergent liquide pour surfaces dures Download PDF

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Publication number
EP0373349A2
EP0373349A2 EP89120518A EP89120518A EP0373349A2 EP 0373349 A2 EP0373349 A2 EP 0373349A2 EP 89120518 A EP89120518 A EP 89120518A EP 89120518 A EP89120518 A EP 89120518A EP 0373349 A2 EP0373349 A2 EP 0373349A2
Authority
EP
European Patent Office
Prior art keywords
composition according
carbon atoms
acid
alkyl
cleaning
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Withdrawn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
EP89120518A
Other languages
German (de)
English (en)
Other versions
EP0373349A3 (fr
Inventor
Birgit Dr. Middelhauve
Frantisek Dr. Jost
Gilbert Dr. Schenker
Eva Dr. Kiewert
Peter Dr. Jeschke
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.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
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 Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP0373349A2 publication Critical patent/EP0373349A2/fr
Publication of EP0373349A3 publication Critical patent/EP0373349A3/fr
Withdrawn legal-status Critical Current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
    • 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
    • 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
    • C11D1/123Sulfonic acids or sulfuric acid esters; Salts thereof derived from carboxylic acids, e.g. sulfosuccinates
    • 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
    • C11D1/37Mixtures of compounds all of which are anionic

Definitions

  • Liquid all-purpose detergents for household and commercial use have taken their place in the past decade because they are easy and straightforward to use.
  • the agents are usually marketed as preferably aqueous concentrates. They can be applied diluted or undiluted to a damp, absorbent cloth of any nature or a sponge, with which the hard surfaces made of metal, lacquered wood, plastic, ceramic products such as porcelain, tiles, tiles and the like can be wiped off and thereby dust, greasy dirt and stains are removed. It is desired that this surface treatment does not leave any detergent stains and strips and does not require any aftertreatment, for example with a damp cloth soaked in clear water.
  • EP 71 411 describes liquid detergent compositions which consist of a mixture of dialkyl sulfosuccinates with anionic and / or nonionic surfactants. These mixtures are said to have good cleaning performance and good foaming properties.
  • EP 112 044 describes liquid detergent compositions comprising dialkyl sulfosuccinates in combination with alkyl ether sulfates which have a special carbon chain distribution.
  • the formulations are characterized by improved performance and assembly.
  • EP 112 045 describes liquid detergent compositions composed of dialkyl sulfosuccinates in combination with other surfactants (e.g. alkyl benzene sulfonates, alkane sulfonates or fatty alcohol ether sulfates) and small amounts of Mg 2+ ions.
  • surfactants e.g. alkyl benzene sulfonates, alkane sulfonates or fatty alcohol ether sulfates
  • Mg 2+ small amounts of Mg 2+ ions.
  • EP 112 047 describes liquid detergent compositions comprising dialkyl sulfosuccinates with alkyl benzene sulfonates, alkane sulfonates and fatty alcohol ether sulfates.
  • the ternary combinations should be characterized by improved performance and packaging properties.
  • No. 3,639,291 describes the synergistic surfactant combination of vicinal alkyl ether sulfates of the formula with 0 ⁇ x ⁇ 15 and 0 ⁇ y ⁇ 15 and 13 ⁇ x + y ⁇ 15 with alkylbenzenesulfonates, in particular for use in manual rinsing.
  • y 0 it follows that the C chain length is 13 ⁇ x ⁇ 15.
  • the surfactants preferably claimed in this document have a maximum C chain length of 12.
  • Liquid cleaning agents are known from US Pat. No. 3,406,208, which can contain water-soluble high-molecular substances as dirt carriers.
  • Water-soluble salts of polyacrylic acid and also water-soluble derivatives of cellulose such as carboxymethyl cellulose are mentioned as examples.
  • liquid general-purpose cleaners which, in addition to water-soluble synthetic surface-active substances, organic solvents and optionally water-soluble builders, contain a small amount of a special water-soluble carboxymethyl cellulose and water.
  • US Pat. No. 3,970,594 discloses liquid, builders-containing cleaning agents for hard surfaces with small amounts of surfactants in combination with small amounts of a mixture of polyvinyl alcohol and / or polyvinylpyrrolidone and polysaccharide salt, which are also said to have improved dirt removal properties.
  • DE 27 09 690 discloses liquid cleaning agents for hard surfaces, which can also contain cleaning-enhancing additives in water-soluble high-molecular substances, such as polyvinyl alcohol, polyvinyl pyrrolidone and carboxymethyl cellulose.
  • liquid cleaning agents for hard surfaces which contain water-soluble polyethylene glycols as cleaning-enhancing additives.
  • alkylbenzenesulfonate and polymer-containing formulations now have an excellent performance profile, that of polymer Free formulations based on surfactants alone have not yet been achieved.
  • Hydroxy mixed ether sulfates produced as described in DE 37 23 354.8, unexpectedly show, together with anionic surfactants which are customary in all-purpose cleaners, no cleaning performance at any mixing ratio as one would expect for good products.
  • the present invention therefore relates to a liquid cleaning agent for hard surfaces based on dilute, preferably aqueous solutions containing anionic surfactants, organic and / or inorganic builders, optionally water-soluble solvents or solubilizers, and other conventional components of such cleaning agents, which is characterized in that it contains, as anionic surfactants, 0.02 to 40, preferably 0.05 to 15% by weight of a mixture of hydroxy mixed ether sulfates and dialkyl sulfosuccinates in a weight ratio of 1:10 to 10: 1, preferably 4: 1 to 1: 4.
  • the hydroxy mixed ether sulfates mentioned are sulfated hydroxyalkyl polyethylene and / or hydroxyalkyl polypropylene glycol ethers of the general formula in the R1 is hydrogen or a linear alkyl radical having 1 to 16, preferably 8 to 12, carbon atoms, R2 is a linear or branched, saturated alkyl radical having 1 to 22, preferably 1 to 16, carbon atoms, R3 is preferably hydrogen, but also a linear alkyl radical having 1 to 16 carbon atoms, R4 is preferably hydrogen, but also a methyl group, M for hydrogen, ammonium, alkylammonium, alkanolammonium, in which the alkyl and alkanol radicals each have 1 to 4 carbon atoms, or a monovalent metal atom and n stands for a number in the range from 0 to 20, preferably 0 to 15, and of mixtures of several such compounds.
  • the dialkyl sulfosuccinates are alkali metal, ammonium or substituted ammonium salts and can be derived from a C7, C8 or C9 alcohol, which can be linear or branched, or from any mixture thereof.
  • the preferred material is the straight chain and branched di-octylsulfosuccinate.
  • the dialkyl sulfosuccinates were prepared by conventional methods, e.g. by esterification of maleic acid and subsequent sulfonation with bisulfite.
  • the anionic surfactants can be present in the form of their alkali, alkaline earth and ammonium salts and as soluble salts of organic bases, such as mono-, di- or triethanolamine.
  • the sodium salts are mostly preferred for cost reasons.
  • alkaline organic or inorganic compounds in particular inorganic or organic complexing agents, are used as framework substances in their entirety, which are preferably present in the form of their alkali or amine salts, in particular the sodium and potassium salts.
  • the alkali hydroxides also belong to the framework substances here.
  • the alkaline polyphosphates in particular the tripolyphosphates and the pyrophosphates, are particularly suitable as inorganic complex-forming framework substances. For reasons of water entrophication, they can be replaced in whole or in part by organic complexing agents.
  • Further inorganic builder substances which can be used according to the invention are, for example, bicarbonates, carbonates, borates, silicates or orthophosphates of the alkalis.
  • the organic complexing agents of the aminopolycarboxylic acid type include, among others, nitrilotriacetic acid, ethylene diamine tetraacetic acid, N-hydroxyethyl ethylene diamine triacetic acid and polyalkylene polyamine N-polycarboxylic acids.
  • di- and polyphosphonic acids examples include: methylenediphosphonic acid, 1-hydroxyethane-1,1-diphosphonic acid, propane-1,2,3-triphosphonic acid, butane-1,2,3,4-tetraphonic acid, polyvinylphosphonic acid, copolymers of vinylphosphonic acid and Acrylic acid, ethane-1,2, dicarboxy-1,2-diphosphonic acid, ethane-1,2-dicarboxy-1,2-dihydroxydiphosphonic acid, phosphonosuccinic acid, 1-aminoethane-1,2-diphosphonic acid, aminotri- (methylenephosphonic acid), methyl amino- or ethylamino-di- (methylenephosphonic acid) and ethylenediamine-tetra- (methylenephosphonic acid).
  • N- or P-free polycarboxylic acids or their salts as builder substances.
  • a large number of these polycarboxylic acids have a complexing ability for calcium. These include e.g. B. citric acid, tartaric acid, benzene hexacarboxylic acid, tetrahydrofuran tetracarboxylic acid, glutaric acid, succinic acid, adipic acid or mixtures thereof.
  • aqueous use solutions have a pH in the range from 7.0 to 10.5 at application concentrations of 2 to 20, preferably 5 to 15 g / l of water or aqueous solution , preferably 7.0 - 9.5
  • an acidic and / or alkaline component also as a buffer, may be required to regulate the pH.
  • Suitable acidic substances are customary inorganic or organic acids or acidic salts, such as, for example, hydrochloric acid, sulfuric acid, bisulfates of alkalis, aminosulfonic acid, phosphoric acid or other acids of phosphorus, in particular the anhydrous acids of phosphorus or their acidic salts or their acid-reacting solid compounds with urea or other lower carboxylic acid amides, partial amides of phosphoric acids or anhydrous phosphoric acid, lactic acid, polycarboxylic acids, such as. B. citric acid, tartaric acid, glutaric acid, succinic acid, adipic acid or mixtures thereof and the like.
  • alkaline builders If the content of alkaline builders is not sufficient to regulate the pH, organic or inorganic compounds such as z.
  • organic or inorganic compounds such as z.
  • solubilizers individually or as mixtures with one another, can be incorporated, for which purpose, in addition to the water-soluble organic solvents such as, in particular, low-molecular aliphatic alcohols having 1-4 carbon atoms, also the so-called hydrotropic substances of the lower alkylarylsulfonate type, for example toluene, xylene or cumene sulfonates or short chain alkyl sulfates such as octyl sulfate. They can also be in the form of their sodium and / or potassium and / or alkylamino salts.
  • Water-soluble organic solvents can also be used as solubilizers, in particular those with boiling points above 75 ° C., such as, for example, the ethers of identical or different polyhydric alcohols or Partial ether from polyhydric alcohols. These include, for example, di- or triethylene glycol polyglycerols and the partial ethers of ethylene glycol, propylene glycol, butylene glycol or glycerol with aliphatic monohydric alcohols containing 1 to 6 carbon atoms in the molecule.
  • ketones such as acetones, methyl ethyl ketone and aliphatic, cycloaliphatic, aromatic and chlorinated hydrocarbons, and also the terpene alcohols.
  • the weight ratio of surfactant to solvent or solubilizer can be 1: 0 to 1: 2, preferably 1: 0.05 to 1: 1.
  • the claimed agents can contain, as other conventional constituents, additives to colorants and fragrances, preservatives and nonionic surfactants known therefor.
  • the cleaning agent to be tested was placed on an artificially soiled plastic surface.
  • the cited contamination 2 was used as artificial soiling.
  • a detergent with 10% by weight of surfactant a mixture of petroleum jelly (R) , fatty acid glycerol esters and pigments was used as the test soiling .
  • the test area of 26 x 28 cm was evenly coated with 2 g of the artificial soiling with the aid of a surface coater.
  • a plastic sponge was impregnated or coated with 10 ml of the surfactant content at 0.1% by weight and the test area was also impregnated or coated with 10 ml of the cleaning agent solution to be tested and moved mechanically on the test area.
  • the test area was also impregnated or coated with 10 ml of the cleaning agent solution to be tested and moved mechanically on the test area.
  • 10 ml of the cleaning agent solution In the case of a 10% strength by weight surfactant solution, only that Test area coated with 10 ml of the detergent solution. After ten wiping movements, the cleaned test area was kept under running water and the loose dirt was removed.
  • the cleaning effect ie the degree of whiteness of the plastic surface cleaned in this way, was measured using an LF 90 photoelectric colorimeter (Dr. B. Lange). The clean white plastic surface served as the white standard.
  • the read values for the cleaned plastic areas are to be equated with the percentage cleaning ability (% RV).
  • % RV percentage cleaning ability
  • the pH of the formulations was adjusted to 7.0 with 50% sodium hydroxide solution.
  • HMS hydroxy mixed ether sulfates
  • Di-isooctylsulfosuccinate, Na salt was used as the dialkyl sulfosuccinate.
  • compositions can also be packaged in the form of spray cleaners.
  • NTA nitrilotriacetic acid
  • EDTA ethylenediaminetetraacetic acid
  • STP sodium tripolyphosphate Sokalan (R)
  • DCS Mixture of glutaric acid, succinic acid and adipic acid from BASF
  • the cleaning services RL rel. [%] with concentrated application, ie with 10% surfactant content, are summarized in the second line.
  • the cleaning performance RL rel. [%] given a total surfactant concentration of 10 wt .-%. After dilution (1: 100) of the recipes with water, the cleaning performance RL rel. [%] determined at the application concentration, ie 0.1% by weight of surfactant.

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  • 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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
EP89120518A 1988-11-14 1989-11-06 Détergent liquide pour surfaces dures Withdrawn EP0373349A3 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3838533 1988-11-14
DE3838533A DE3838533A1 (de) 1988-11-14 1988-11-14 Fluessiges reinigungsmittel fuer harte oberflaechen

Publications (2)

Publication Number Publication Date
EP0373349A2 true EP0373349A2 (fr) 1990-06-20
EP0373349A3 EP0373349A3 (fr) 1990-07-11

Family

ID=6367125

Family Applications (2)

Application Number Title Priority Date Filing Date
EP89120518A Withdrawn EP0373349A3 (fr) 1988-11-14 1989-11-06 Détergent liquide pour surfaces dures
EP89913003A Pending EP0436671A1 (fr) 1988-11-14 1989-11-06 Produit a nettoyer liquide pour surfaces dures

Family Applications After (1)

Application Number Title Priority Date Filing Date
EP89913003A Pending EP0436671A1 (fr) 1988-11-14 1989-11-06 Produit a nettoyer liquide pour surfaces dures

Country Status (8)

Country Link
EP (2) EP0373349A3 (fr)
JP (1) JPH04501733A (fr)
KR (1) KR900701983A (fr)
BR (1) BR8907769A (fr)
CA (1) CA2002339A1 (fr)
DE (1) DE3838533A1 (fr)
TR (1) TR24128A (fr)
WO (1) WO1990005770A2 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4122200A1 (de) * 1991-07-04 1993-01-07 Henkel Kgaa Waessrige zubereitungen oberflaechenaktiver substanzen

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0112044A1 (fr) * 1982-11-16 1984-06-27 Unilever N.V. Compositions détergentes
EP0164894A2 (fr) * 1984-05-11 1985-12-18 Unilever N.V. Compositions détergentes

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0112044A1 (fr) * 1982-11-16 1984-06-27 Unilever N.V. Compositions détergentes
EP0164894A2 (fr) * 1984-05-11 1985-12-18 Unilever N.V. Compositions détergentes

Also Published As

Publication number Publication date
KR900701983A (ko) 1990-12-05
BR8907769A (pt) 1991-08-27
WO1990005770A3 (fr) 1990-07-12
WO1990005770A2 (fr) 1990-05-31
DE3838533A1 (de) 1990-05-17
EP0436671A1 (fr) 1991-07-17
TR24128A (tr) 1991-03-29
CA2002339A1 (fr) 1990-05-14
JPH04501733A (ja) 1992-03-26
EP0373349A3 (fr) 1990-07-11

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