EP1075502A1 - Produit pour laver la vaisselle a action antibacterienne - Google Patents

Produit pour laver la vaisselle a action antibacterienne

Info

Publication number
EP1075502A1
EP1075502A1 EP98924255A EP98924255A EP1075502A1 EP 1075502 A1 EP1075502 A1 EP 1075502A1 EP 98924255 A EP98924255 A EP 98924255A EP 98924255 A EP98924255 A EP 98924255A EP 1075502 A1 EP1075502 A1 EP 1075502A1
Authority
EP
European Patent Office
Prior art keywords
weight
alkylbenzenesulfonates
composition according
salts
amounts
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
EP98924255A
Other languages
German (de)
English (en)
Other versions
EP1075502B1 (fr
Inventor
Dagmar Zaika
Brigitte Giesen
Christian Laske
Hans Andree
Michael Heinzel
Norbert Stelter
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 EP1075502A1 publication Critical patent/EP1075502A1/fr
Application granted granted Critical
Publication of EP1075502B1 publication Critical patent/EP1075502B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2075—Carboxylic acids-salts thereof
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/34—Organic compounds containing sulfur
    • C11D3/3409—Alkyl -, alkenyl -, cycloalkyl - or terpene sulfates or sulfonates

Definitions

  • the invention relates to dishwasher detergents containing alkylbenzoisulfonate which, when used in concentrated form, show an antibacterial effect, i.e. when used undiluted, inhibit bacterial growth and, in addition, kill a large number of bacteria.
  • a modern hand dishwashing detergent must also have a special range of properties, which includes very good cleaning, skin tolerance, temperature and storage stability and ecological compatibility.
  • Antibacterial detergents are known in the prior art.
  • a bacteriostatic component i.a. Triclosan (2,4,4'-trichloro-2'-hydroxydiphenyl ether)
  • natural or nature-identical extracts e.g. Extracts from the orange peel using pineapple oil, geraniol, nerol etc.
  • the bacteriostatic effect is not sufficient to guarantee sufficient inhibition of bacterial growth when using the hand dishwashing liquid using moist dishcloths, sponges or brushes.
  • Chloramine-T toluenesulfonic acid chloramide sodium salt
  • Germal 115 imidazolidinyl urea
  • sodium formate 2-phenoxyethanol, 1-phenoxy-2-propanol, 2-phenoxy-1-propanol showed insufficient antibacterial effects, especially at 50% concentration Effect.
  • compositions proposed in the prior art is suitable as an arbitrarily perfumable, very easy-cleaning, skin-compatible, temperature- and storage-stable and ecologically compatible hand dishwashing detergent with specific anti- bacterial effectiveness when concentrated on wet work surfaces, kitchen appliances using wet dishcloths, sponges and brushes.
  • Products that are easy to perfume, very easy to clean, skin-compatible, temperature- and storage-stable and ecologically compatible products with good antibacterial activity when used in concentrated form are obtained by mixing a surfactant-containing mixture with alkylbenzenesulfonate and possibly other surfactants, especially fatty alcohol ether sulfate, but also alkyl polyglycoside and betaine , together with benzoic acid or its salts.
  • the present invention accordingly relates to a hand dishwashing detergent with good antibacterial activity, comprising anionic surfactants, the detergent containing one or more alkylbenzenesulfonates and, as the antibacterial active component, benzoic acid and / or one or more of their salts.
  • the present invention also relates to the use of benzoic acid and / or one or more of its salts as an antibacterial component in hand dishwashing detergents containing alkylbenzenesulfonate.
  • Benzoic acid salts for the purposes of the present invention are in particular the sodium, potassium, magnesium or calcium salts and also mixtures thereof, which can be used alone or together with benzoic acid in the agents according to the invention.
  • benzoic acid salts or benzoic acid if necessary together with the corresponding hydroxides, i.e. Sodium, potassium, magnesium or Calcium hydroxide can be used.
  • a content of benzoic acid and / or its salts is from 0.1 to 8% by weight, preferably from 0.5 to 6% by weight and particularly preferably preferably from 1 to 4% by weight.
  • a detergent formulation containing benzoic acid and / or benzoic acid salt at a pH in the finished product between 4 and 6, preferably between 4.5 and 5.5, in particular between 4.9 and 5.3, has the strongest antibacterial activity combined with the best storage stability.
  • the pH of the agents according to the invention can be adjusted by means of customary pH regulators, for example citric acid or sodium hydroxide.
  • Alkylbenzenesulfonates in the sense of the teaching according to the invention are alkylbenzenesulfonates with straight-chain or branched, saturated or unsaturated C 6 -C 12 -alkyl radicals, preferably C 8 .
  • 18 -alkyl radicals in particular C 1-4 -alkylene radicals, most preferably C 10 . 13 alkyl residues. They are used as alkali metal and / or alkaline earth metal salts, in particular sodium, potassium, magnesium and / or calcium salts, as well as ammonium salts or mono-, di- or triethanolammonium salts but also as alkylbenzenesulfonic acid together with the corresponding alkali metal or Alkaline earth metal hydroxide and / or ammonia or mono-, di- or triethanolamine used.
  • the incorporation of benzoic acid or benzoic acid salts succeeds without problems if the alkylbenzenesulfonates are used partially or completely in the form of their mono-, di- or trialkanolammonium salts, in particular triethanolammonium salts.
  • the agents accordingly contain 0 mono-, di- or trialkanolammonium alkylbenzenesulfonate, in particular triethanoiammonium alkylbenzenesulfonate, in amounts of from 10 to 100%, preferably from 30 to 100, based on the total amount by weight of alkylbenzenesulfonates %, in particular from 50 to 100%.
  • the agents contain exclusively mono-, di- and / or trialkanolammonium alkylbenzenesulfonate, in particular triethanoiammonium alkylbenzenesulfonate, as 25 alkylbenzenesulfonates.
  • the incorporation of benzoic acid or benzoates is also successful if the agents contain a combination of alkylbenzenesulfonates with one or more fatty alcohol ether sulfates.
  • the agents contain alkylbenzenesulfonates and fatty alcohol ether sulfates in a weight ratio of from 10: 1 to 1: 5, preferably from 5: 1 to 1: 2, in particular from 2: 1 up to 1: 1.5.
  • only mono-, di- or trialkanolammonium alkylbenzenesulfonates are contained on average as alkylbenzenesulfonates.
  • anionic surfactants can be aliphatic sulfates such as fatty alcohol sulfates, diaikyl ether sulfates, monoglyceride sulfates and aliphatic sulfonates such as alkane sulfonates, olefin sulfonates, ether sulfonates, n-alkyl ether sulfone sulfates, and n-alkyl ether sulfone sulfates.
  • Fatty acid cyanamides, sulfosuccinic acid esters, fatty acid isethionates, acylaminoalkane sulfonates (fatty acid taurides), fatty acid sarcosinates, ether carboxylic acids and alkyl (ether) phosphates can also be used in the context of the present invention.
  • the fatty alcohol ether sulfates are particularly preferred in the context of the present invention. Fatty alcohol sulfates and combinations of fatty alcohol ether sulfates and fatty alcohol sulfates are also preferred.
  • fatty acids or fatty alcohols or their derivatives are representative of branched or unbranched carboxylic acids or alcohols or their derivatives, preferably having 6 to 22 carbon atoms.
  • the former are preferred for ecological reasons, in particular because of their vegetable basis than based on renewable raw materials, but without restricting the teaching according to the invention to them.
  • the oxo alcohols or their derivatives obtainable, for example, according to ROELE ⁇ / oxo synthesis can also be used accordingly.
  • Fatty alcohol ether sulfates are products of sulfation reactions on alkoxylated alcohols.
  • alkoxylated alcohols generally understands alkoxylated alcohols to mean the reaction products of alkylene oxide, preferably ethylene oxide, with alcohols, preferably the longer-chain alcohols in the sense of the present invention.
  • a complex mixture of addition products of different degrees of ethoxylation are formed from n moles of ethylene oxide and one mole of alcohol, depending on the reaction conditions.
  • Another embodiment consists in the use of mixtures of the alkylene oxides, preferably the mixture of ethylene oxide and propylene oxide.
  • Low-ethoxylated fatty alcohols (0.5 to 4 mol EO, preferably 1 to 2.5 mol EO) are very particularly preferred for the purposes of the present invention.
  • the anionic surfactants are preferably used in amounts of 0.2 to 40% by weight, in particular 3 to 35% by weight, particularly preferably 5 to 30% by weight.
  • Particularly suitable surfactant mixtures are those composed of anionic surfactants in combination with one or more nonionic surfactants or betaine surfactants, the betaine surfactant in this connection being equated with the class of amphoteric surfactants.
  • the joint additional use of nonionic surfactants and betaine surfactants in a mixture can also be advantageous for many applications.
  • the surfactants are used in amounts of 0.2 to 50% by weight, preferably 1 to 40% by weight, in particular 3 to 35% by weight and extremely preferably 5 to 30% by weight.
  • Nonionic surfactants in the context of the present invention can be alkoxylates such as polyglycol ethers, fatty alcohol polyglycol ethers, alkylphenol polyglycol ethers, end-capped polyglycol ethers, mixed ethers and hydroxy mixed ethers and fatty acid polyglycol esters. Ethylene oxide, propylene oxide, block polymers and fatty acid alkanolamides and fatty acid polyglycol ethers can also be used.
  • An important class of nonionic surfactants that can be used according to the invention are the polyol surfactants and here in particular the glucose surfactants, such as alkyl polyglycoside and fatty acid glucamides. The alkyl polyglucosides are particularly preferred.
  • Alkyl polyglycosides are surfactants which can be obtained by the reaction of sugars and alcohols according to the relevant methods of preparative organic chemistry, which, depending on the type of production, results in a mixture of monoalkylated, oligomeric or polymeric sugars.
  • Preferred alkyl polyglycosides can be alkyl polyglucosides, the alcohol being particularly preferably a long-chain fatty alcohol or a mixture of long-chain fatty alcohols with branched or unbranched C 8 to C 18 alkyl chains and the degree of oligomerization (DP) of the sugars between 1 and 10, preferably 1 to 6, in particular 1.1 to 3, most preferably 1.1 to 1.7.
  • DP degree of oligomerization
  • the agents preferably contain nonionic surfactants in amounts of 0.1 to 14.9% by weight, in particular 0.5 to 8% by weight and extremely preferably 1 to 6% by weight.
  • betaine surfactants which can be used according to the invention include the alkyl betaines, the alkyl amido betaines, the imidazolinium betaines and the aminopropionates. just like the sulfobetaines and biosurfactants.
  • a preferred ingredient here is alkylamido betaine.
  • betaine surfactants are preferably used in amounts of 0.05 to 10% by weight, in particular 0.1 to 7% by weight, most preferably 0.2 to 5% by weight.
  • solvents for example alcohols, preferably low molecular weight alkanols with 1 to 4 carbon atoms in the molecule, in particular ethanol and isopropanol. They contribute to the incorporation of perfume and dye, prevent the formation of liquid-crystalline phases and improve the cold stability of the clear formulations.
  • solubilizers for example alkanolamines, polyols such as ethylene glycol, 1,2-propylene glycol, glycerol and other mono- and polyhydric alcohols as well as alkylbenzenesulfonates with 1 to 3 carbon atoms in the alkyl radical, in particular cumene, also has an advantageous effect in the agents according to the invention -, toluene and xylene sulfonate, in amounts of up to 5% by weight, preferably 0.05 to 3% by weight, in particular 0.1 to 2% by weight.
  • solubilizers for example alkanolamines, polyols such as ethylene glycol, 1,2-propylene glycol, glycerol and other mono- and polyhydric alcohols as well as alkylbenzenesulfonates with 1 to 3 carbon atoms in the alkyl radical, in particular cumene
  • ingredients common in hand dishwashing detergents such as UV stabilizers, defoamers (such as silicone oils, paraffin oils or mineral oils), structuring agents, perfume substances, dyes, corrosion inhibitors, preservatives or the like, preferably in amounts of up to 5% by weight.
  • the hand dishwashing detergents according to the invention can be obtained by stirring the individual components in any order and leaving the mixture to stand until 8th
  • Agents E1 to E5 according to the invention were prepared as described above and their pH, viscosity, clouding or clearing point, and in some cases also their antibacterial activity and rinsing power were determined.
  • compositions of the agents E1 to E5 according to the invention in% by weight and the specific properties are shown in Table 1.
  • agents E1 to E5 according to the invention contained traces of dye.
  • the pH of the agents E1 to E5 according to the invention was adjusted with citric acid.
  • the viscosity was measured at 20 ⁇ C with a viscometer of the type Brookfield LV DV 11+ determined (spindle 25, shear rate 30 min -1).
  • the cold cloud point was determined by cooling a sample in the cryostat with a cooling rate of 0.2 ° C.min * 1 , the cold cloud point being the temperature at which a slight cloudiness was first detected. After the sample was completely cloudy, the mixture was heated at a heating rate of 0.2 ° C min '1 . The temperature at which the sample was completely clear for the first time is given as the clear point.
  • the rinsing capacity of the agents E1 to E3 and E5 according to the invention was determined in a semi-automatic plate test apparatus using two different types of soiling (beef tallow or soiling or olive oil / soiled pork). Plates soiled with the test dirt were washed at a constant temperature of 40 or 45 ° C in 5 l of water with 16 ° German hardness under constant conditions compared to a high-quality classic hand dishwashing liquid as a laboratory standard until the foam - formed before the start of the test - was destroyed was and the plates were no longer clean. The concentration of the agent was 4 ml per 5 l of water. The number of plates rinsed is set in relation to the laboratory standard with a rinsing capacity of 100% (the mean value for both stains is given). 10
  • Test method quantitative suspension test based on the DGHM test method (the logarithmic reduction rate is given)
  • Test germ Salmonelle enteritidis (practice isolate)
  • Test concentration 50% in water of 17 ° German hardness Test temperature: room temperature Exposure time: 15 minutes
  • Test method quantitative suspension test based on the European standard EN 1040 test organisms: Staphylococcus aereus, Pseudomonas aeruginosa,

Abstract

Un produit pour laver la vaisselle à la main, parfumable à volonté, présentant de très bonnes caractéristiques de nettoyage, de tolérance cutanée, de stabilité en température et au stockage et de respect de l'environnement, alliées à une efficacité antibactérienne spécifique lors d'une utilisation concentrée sur des surfaces de travail et des ustensiles de cuisine humides avec des lavettes, des éponges et des brosses humides, est préparé sous forme d'un mélange contenant des agents de surface anioniques. Ce mélange contient un ou plusieurs sulfonates de benzène d'alkyle ainsi que de l'acide benzoïque et/ou un ou plusieurs de ses sels. L'acide benzoïque ou ses sels conviennent pour être utilisés comme constituants actifs antibactériens dans des produits pour laver la vaisselle à la main contenant du sulfonate de benzène d'alkyle.
EP98924255A 1998-04-30 1998-04-30 Produit pour laver la vaisselle a action antibacterienne Expired - Lifetime EP1075502B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/EP1998/002565 WO1999057235A1 (fr) 1998-04-30 1998-04-30 Produit pour laver la vaisselle a action antibacterienne

Publications (2)

Publication Number Publication Date
EP1075502A1 true EP1075502A1 (fr) 2001-02-14
EP1075502B1 EP1075502B1 (fr) 2005-10-12

Family

ID=8166947

Family Applications (1)

Application Number Title Priority Date Filing Date
EP98924255A Expired - Lifetime EP1075502B1 (fr) 1998-04-30 1998-04-30 Produit pour laver la vaisselle a action antibacterienne

Country Status (9)

Country Link
EP (1) EP1075502B1 (fr)
CN (1) CN1291225A (fr)
AT (1) ATE306533T1 (fr)
DE (1) DE59813107D1 (fr)
ES (1) ES2249831T3 (fr)
HU (1) HUP0103189A2 (fr)
SK (1) SK16202000A3 (fr)
TR (1) TR200002723T2 (fr)
WO (1) WO1999057235A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105524731A (zh) * 2014-09-30 2016-04-27 青岛康和食品有限公司 一种含有抗过敏成分的洗洁精

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10023438A1 (de) * 2000-05-12 2001-11-22 Henkel Kgaa Konzentrat zur Verdünnung unter Viskositätserhalt oder -erhöhung
DE10122380A1 (de) * 2001-05-09 2002-11-28 Schuelke & Mayr Gmbh Alkoholfreies Flüssig-Konzentrat zur Konservierung von kosmetischen, Haushalts- und technischen Produkten
GB0112567D0 (en) * 2001-05-24 2001-07-18 Cussons Int Ltd Bactericidal liquid detergent composition
EP1331261A1 (fr) * 2002-01-23 2003-07-30 Chemische Fabrik Dr. Weigert GmbH & Co. KG. Procès de nettoyage et désinfection de la vaiselle
DE102009005791A1 (de) 2009-01-22 2010-07-29 Henkel Ag & Co. Kgaa Handgeschirrspülmittel mit antibakterieller Wirkung
CN104194970A (zh) * 2014-09-29 2014-12-10 镇江华域环保设备制造有限公司 一种餐具专用洗洁精
CN106318678A (zh) * 2016-07-25 2017-01-11 广州普爱生物科技有限公司 无水无防腐剂无酒精的蛋白酶超浓缩洗衣液

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2226988A1 (de) * 1972-06-02 1973-12-20 Henkel & Cie Gmbh Geschirrspuel- und reinigungsmittel
US4867898A (en) * 1987-03-23 1989-09-19 American Cyanamid Company Broad spectrum antimicrobial system for hard surface cleaners
NZ240355A (en) * 1991-06-04 1994-09-27 Ecolab Inc Sanitising composition comprising sorbic and benzoic acids
DE4417809A1 (de) * 1994-05-20 1995-11-23 Becker Klaus Verfahren zur Sanitärreinigung sowie ein Sanitärreiniger
US5510052A (en) * 1994-08-25 1996-04-23 Colgate-Palmolive Co. Enzymatic aqueous pretreatment composition for dishware

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9957235A1 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105524731A (zh) * 2014-09-30 2016-04-27 青岛康和食品有限公司 一种含有抗过敏成分的洗洁精

Also Published As

Publication number Publication date
EP1075502B1 (fr) 2005-10-12
ES2249831T3 (es) 2006-04-01
DE59813107D1 (de) 2006-02-23
WO1999057235A1 (fr) 1999-11-11
HUP0103189A2 (hu) 2002-01-28
SK16202000A3 (sk) 2001-04-09
TR200002723T2 (tr) 2000-12-21
ATE306533T1 (de) 2005-10-15
CN1291225A (zh) 2001-04-11

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