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
  • C11D3/16—Organic compounds
  • C11D3/18—Hydrocarbons
  • C11D3/188—Terpenes
• • 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
  • C11D3/2003—Alcohols; Phenols
  • C11D3/2006—Monohydric alcohols
  • C11D3/2034—Monohydric alcohols aromatic
• • 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
  • C11D3/2003—Alcohols; Phenols
  • C11D3/2006—Monohydric alcohols
  • C11D3/2037—Terpenes
• • 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
  • C11D3/2003—Alcohols; Phenols
  • C11D3/2041—Dihydric alcohols
  • C11D3/2062—Terpene
• • 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
  • C11D3/2068—Ethers
• • 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
  • C11D3/2072—Aldehydes-ketones
• • 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
  • C11D3/2093—Esters; Carbonates
• • 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
  • C11D3/22—Carbohydrates or derivatives thereof
  • C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
• • 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
  • C11D3/22—Carbohydrates or derivatives thereof
  • C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
  • C11D3/225—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin etherified, e.g. CMC
• • 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
  • C11D3/37—Polymers
  • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • C11D3/3707—Polyethers, e.g. polyalkyleneoxides
• • 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
  • C11D3/37—Polymers
  • C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
  • C11D3/3753—Polyvinylalcohol; Ethers or esters 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
  • C11D3/37—Polymers
  • C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
  • C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid 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
  • C11D3/37—Polymers
  • C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
  • C11D3/3769—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
  • C11D3/3776—Heterocyclic compounds, e.g. lactam
• • 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
  • C11D3/50—Perfumes
• • 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
  • C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
  • C11D7/22—Organic compounds
  • C11D7/24—Hydrocarbons
  • C11D7/248—Terpenes
• • 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
  • C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
  • C11D7/22—Organic compounds
  • C11D7/26—Organic compounds containing oxygen
  • C11D7/261—Alcohols; Phenols
• • 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
  • C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
  • C11D7/22—Organic compounds
  • C11D7/26—Organic compounds containing oxygen
  • C11D7/263—Ethers
• • 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
  • C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
  • C11D7/22—Organic compounds
  • C11D7/26—Organic compounds containing oxygen
  • C11D7/264—Aldehydes; Ketones; Acetals or ketals
• • 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
  • C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
  • C11D7/22—Organic compounds
  • C11D7/26—Organic compounds containing oxygen
  • C11D7/266—Esters or carbonates

Definitions

• the invention is in the field of hard surface cleaning, especially in the field of hard surface cleaning composition having anti-microbial effect.
• Hygiene is of high priority to present day consumers. Consumers all over the world use various kinds of disinfecting cleaning compositions for hard surfaces.
• E . coli Escherichia coli
• Staphylococcus aureus also referred to as S . aureus.
• S . aureus Several other gram-positive and gram-negative bacteria can be found on any household surface.
• hypochlorite The most commonly known disinfectant in house hold care is hypochlorite.
• hypochlorite causes bad smell, bleaches clothes that come in contact with it and is unpleasant to skin mostly caused by its high alkalinity.
• EP-A-912678 discloses the use of essential oil compounds for anti microbial effect on hard surfaces.
• essential oils are relatively expensive ingredients. Additionally, essential oils are also known for their fragrances; using high amounts may cause a peculiar smell that is not always appreciated by the consumer.
• WO1998/20735 (Procter and Gamble) describes a spray-able liquid disinfecting composition comprising a hydrogen peroxide, an antimicrobial essential oil, and a shear thinning polymeric thickener.
• the hydrogen peroxide in presence shear thinning polymeric thickener provides safe and effective disinfection on clean surfaces.
• the Application doesn't disclose a composition comprising a polymer complex and an antimicrobial composition.
• the hygiene benefit is not only active shortly after deposition, but remains on the surface for a longer time.
• composition that is effective against common bacteria, including both gram-positive and gram-negative bacteria.
• composition comprising a low amount of essential oil and quaternary ammonium biocide and a polymer complex provides improved hygiene efficacy.
• the present invention provides in a first aspect a hard surface treatment composition
• a hard surface treatment composition comprising a polymer complex comprising polymer A selected from the group of homopolymers and copolymers of carboxylic acid, and a polymer B selected from the group of homopolymers and copolymers of alkylene oxides, vinyl pyrrolidone; and/or the group of homopolymers and copolymers of vinyl alcohol, saccharides, hydroxyalkyl cellulose, wherein polymer A and polymer B are not of the same class and wherein Polymer B has a monomeric unit comprising a group that forms hydrogen bonds with the carboxyl groups of polymer A; and an antimicrobial composition comprising essential oil and a quaternary ammonium biocide, wherein the pH of the hard surface treatment composition is between 2 and less than 6.
• the invention provides a method for providing an anti-microbial effect to a hard surface comprising the steps of applying a composition according to the first aspect to the surface, and waiting for at least 5 seconds.
• the invention provides the use of a combination of a polymer complex comprising polymer A selected from the group of homopolymers and copolymers of carboxylic acid, and a polymer B selected from the group of homopolymers and copolymers of alkylene oxides, vinyl pyrrolidone; and/or the group of homopolymers and copolymers of vinyl alcohol, saccharides, hydroxyalkyl cellulose; wherein polymer A and polymer B are not of the same class and wherein polymer B has a monomeric unit comprising a group that forms hydrogen bonds with the carboxyl groups of polymer A; and an antimicrobial composition comprising essential oil and a quaternary ammonium biocide, wherein the pH of the hard surface treatment composition is between 2 and less than 6, for providing a anti-microbial effect on hard surfaces.
• anti-microbial effect is meant being able to kill bacteria under the standard European suspension test (EST) - EN 1276.
• composition according to the invention thus comprises a polymer complex and an antimicrobial composition.
• the polymer complex according to the invention comprises a polymer A selected from the group of homopolymers and copolymers of carboxylic acid, and a polymer B selected from the group of homopolymers and copolymers of alkylene oxides, vinyl pyrrolidone ; and/or the group of homopolymers and copolymers of vinyl alcohol, saccharides, hydroxyalkyl cellulose ;
• composition according to the invention comprises a polymer A and a polymer B.
• Polymers A and B are typically selected such that they form a complex due to the formation of hydrogen bonds.
• the polymers may be homo polymers or copolymers, wherein by copolymer of monomer X is meant any polymer that contains the monomer X and at least one further monomer.
• Polymers A and B are preferably present in the composition in a ratio of between 1:5 and 5:1, more preferably between 1:2 and 2:1
• polymer A is a polymer selected from the group of homopolymers and copolymers of carboxylic acid.
• Polymer A has a plurality of carboxyl groups.
• the polymer A has a molecular mass preferably from 300 to 10 9 D (Dalton, also referred to as atomic mass units, amu).
• the polymer A is selected from the class consisting of homopolymers or copolymers of carboxylic polymers, including natural synthetic and semi-synthetic polymers in this class.
• polymer A according to the present invention include:
• Homopolymers or copolymers of carboxylic acid have a molecular mass of preferably from 2x10 3 to 10 7 D more preferably from 5x10 4 to 10 6 D and most preferably from 9x10 4 to 5x10 5 D.
• the particle size is preferably less than 200 ⁇ m, preferably less than 100 ⁇ m, more preferably less than 50 ⁇ m still more preferably less than 10 ⁇ m, or even less than 5 ⁇ m.
• the homopolymers or copolymers of polysaccharide have a molecular mass of preferably from 10 3 to 10 9 D, more preferably from 10 4 to 10 9 D and most preferably from 10 5 to 10 9 D.
• Polymer A is preferably at least partially neutralised in the Sodium (Na + ) form, preferably at least 10%w of polymer A is neutralised, more preferably at least 20%, still more preferably at least 50%.
• Polymer A may be synthetic, semi-synthetic or natural. However, synthetic or semi-synthetic polymers are preferred.
• Polymer A is preferably water soluble or water dispersible, most preferably polymer A is water soluble.
• the polymer A is selected from a class consisting of homopolymers or copolymers of carboxylic acid.
• the homopolymers or copolymers of carboxylic acid are preferably a polyacrylic acid or a copolymer thereof.
• Examples include SOKALAN® PA (BASF) and CARBOPOL® (Lubrizol).
• the concentration of polymer A in the composition according to the invention is preferably between 0.001 and 25% by weight, more preferably at least 0.002%, or even at least 0.005%, but preferably not more than 15%, more preferably less than 5%, still more preferably less than 1%, even more preferably less than 0.5%, even less than 0.1%, or even less than 0.05% by weight of the composition.
• polymer B has a monomeric unit comprising a group that forms hydrogen bonds with the carboxyl groups of polymer A.
• polymer B is selected from the group of homopolymers and copolymers of alkylene oxides, vinyl pyrrolidone; and/or the group of homopolymers and copolymers of vinyl alcohol, saccharides, hydroxyalkyl cellulose.
• the group of homopolymers and copolymers of vinyl alcohol, saccharides, hydroxyalkyl cellulose, is generally not water soluble.
• the particle size is set such that the particles are easily dispersible in water or and aqueous solution (i.e. a wash or rinse liquor). If the polymers are in particulate form, the particle size is preferably less than 200 ⁇ m, more preferably less than 100 ⁇ m, even more preferably less than 50 ⁇ m still more preferably less than 10 ⁇ m, or even less than 5 ⁇ m.
• polymer A and polymer B are not of the same class.
• Polymers A and B are selected from different classes of polymers. Without wishing to be limited by theory, it is believed that the two polymers A and B, when dissolved in water, form a complex with a solubility lower than each of the polymers A and B, which helps in enhanced deposition and other benefits.
• Polymer B preferably has a molecular mass from 10 3 to 10 9 D.
• Homopolymers or copolymers of vinyl pyrrolidone or vinyl alcohol preferably have a molecular mass of between 10 3 and 10 7 D, more preferably from 10 4 to 10 6 D and most preferably from 30,000 to 500,000 D.
• Commercially available polyvinyl pyrrolidone can be used, one example of which is LUVISKOL® (BASF).
• Homopolymers or copolymers of poly alkylene oxide preferably have a molecular mass greater than 2x10 4 D.
• the molecular mass is preferably from 2x10 4 to 10 6 D, more preferably from 3x10 4 to 5x10 5 D and most preferably from 5x10 4 to 2x10 5 D.
• Homopolymers or copolymers of saccharide preferably have a molecular mass of preferably from 10 3 to 10 9 D, more preferably from 10 4 to 10 9 D and most preferably from 10 5 to 10 9 D.
• Any commercially available poly alkylene oxide, for example POLYOX® (Dow Chemical Co) can be used according to the present invention.
• Polymer B may be synthetic, semi-synthetic or natural. However, synthetic or semi-synthetic polymers are preferred.
• the polymer B is water soluble.
• the polymer B is selected from a class consisting of homopolymers or copolymers of vinyl pyrrolidone or alkylene oxide.
• the concentration of polymer B in the composition according to the invention is preferably between 0.001 and 20% by weight, more preferably at least 0.002%, or even at least 0.005%, but preferably not more than 10%, more preferably less than 5%, still more preferably less than 1%, even more preferably less than 0.5%, even less than 0.1 %, or even less than 0.05% by weight of the composition.
• the most preferred combinations of the polymers are PAA-PVP, PAA-PEO, PAA-PEG Starch-graft-polymethacrylic acid-Polyethylene Oxide.
• the polymer complex according to the invention comprises an antimicrobial composition comprising essential oil and quaternary ammonium biocide.
• Essential oils are typically concentrated, hydrophobic liquid containing volatile aroma compounds from plants.
• Essential oils are also known as volatile, ethereal oils or aetherolea.
• An oil is "essential” in the sense that it carries a distinctive scent, or essence, of the plant.
• Essential oils do not as, a group, need to have any specific chemical properties in common, beyond conveying characteristic fragrances.
• Essential oils may also be obtained though synthetic or semi-synthetic routes.
• Essential oils are generally extracted by distillation. Other processes include expression, or solvent extraction. They are used in perfumes, cosmetics, soap and other products, for flavoring food and drink, and for scenting incense and household cleaning products.
• aromatic essential oils suitable for use in the present invention include amyl salicylate, carvacrol, cymene, e.g. p-cymene, dihydroeugenol, eugenol, hexyl eugenol, hexyl salicylate, isoeugenol, methyl eugenol, methyl isoeugenol, methyl salicylate, tert butyl cresol, thymol, and vanillin.
• non-aromatic essential oils of terpenoid compounds include cedrene, cineole, citral (including geranial and neral), citronellal, citronellol, eucalyptol (also known as 1,8 cineole) paradihydrolinalool, dihydromyrcenol (DH myrcenol), farnesol, geraniol, hexyl cinnamaldehyde, hydroxycitronallol, hydroxycitronellal, isocitral, limonene, preferably d-limonene, linalool, longifolene, menthol, nerol, nerolidiol, pinene, e.g.
• ⁇ -pinene phellendrene
• terpinene e.g. ⁇ -terpinene and ⁇ -terpinene
• terpineol e.g. ⁇ -terpineol and terpin-4-ol
• THM tetrahydromyrcenol
• the most preferred essential oils in the context of the present invention are thymol, terpineol and eugenol.
• the essential oil is preferably present in the composition in a concentration of between 0.001 and 10% by weight of the composition, but preferably at least 0.002%, or even at least 0.005% by weight of the composition, while preferably not more than 5%, more preferably not more than 1%, still more preferably not more than 0.5%, or even not more than 0.1% by weight of the concentration.
• composition comprises a second essential oil, wherein the essential oils are even more preferably selected from any combination of a thymol, a terpineol and/or a eugenol.
• composition comprises three essential oils, wherein the essential oils are still more preferably selected from a combination of a thymol, a terpineol and a eugenol.
• the above mentioned concentrations may be considered to be the concentrations of the combined essential oils, but preferably relate to each of the individual essential oils.
• a quaternary ammonium biocide is used to provide additional biocidal efficacy.
• the quaternary ammonium biocide is preferably selected from Cetyl-trimethyl-ammonium Chloride, Cetyl-trimethyl-ammonium Bromide, Tetradecyl-trimethyl-ammonium Chloride, Dodecyl-trimethyl-ammonium Chloride, Stearyl-trimethyl-ammonium Chloride, Octadecyl-trimethyl-ammonium Chloride, Dodecylpyridinium Chloride, Cetylpyridinium Chloride, Benzalkonium Chloride, Tetrabutyl-ammonium Chloride, Tetraheptyl-ammonium Chloride, 1,3-Decyl-2-methyl-imidazolium Chloride, 1-Hexadecyl-3-methyl-imidazolium Chloride, Didecyl-dimethyl-ammonium Bromide, Didecy
• Bromides are typically not preferred due to their toxicity.
• the most preferred quaternary ammonium biocide is benzalkonium chloride and cetylpyridinium chloride.
• the quaternary ammonium biocide is preferably present in the composition in a concentration of between 0.01 and 10% by weight of the composition, but preferably at least 0.02%, or even at least 0.05% by weight of the composition, while preferably not more than 5%, more preferably not more than 1%, still more preferably not more than 0.5%, or even not more than 0.1% by weight of the concentration.
• the quaternary ammonium biocide provides more complete kill with longer lasting hygiene.
• compositions according to the invention may be applied in various hard surface cleaning composition, such as concentrated and dilute liquid compositions.
• Concentrated composition include amongst other floor cleaner composition that need to be diluted by the consumers upon use.
• concentrations are relating to the diluted concentrations as used by the consumer.
• Dilute liquid compositions include but are not limited to ready-to-use compositions, such as liquid abrasive cleaners and toilet cleaning compositions, and spray compositions for glass, kitchen surfaces and bathroom surfaces
• the contact time of the product with the surface before rinsing is at least 5 seconds, more preferably at least 10 seconds, still more preferably at least 15 seconds, or even at least 20 seconds.
• compositions may stay for a longer period of time, preferably at least 5 minute, more preferably at least 15 minutes, still more preferably at least 1 hour, still more preferably at least 2 hours, or even more than 5 hours, or even days.
• the pH of the compositions is between pH 2 and less than pH 6, still more preferably at least pH 3.
• composition is not wiped away or rinsed, but may be wiped of after the indicated time.
• Example 1 EST challenge This test is not a surface test. It is a suspension test
• the standard European suspension test (EST) protocol - EN 1276 for antiseptics was followed.
• the test organisms were Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus, and Enterococcus hirae. Under clean conditions the test was done with 0.03% BSA (bovine serum albumin), while in dirty condition 0.3% BSA was used (see table 2 below).
• BSA bovine serum albumin
• the contact time was 5 min. A 5 log reduction was required to pass the test.
• compositions as used are given in table 1 below.
• the polymer complex comprised PAA (poly acrylic acid; Mw 100,000 D, ex Sigma-Aldrich) and PEO (poly ethylene oxide; Mw 100,000 D, ex Sigma-Aldrich), in a total amount as given in the table.
• Table 2 E. coli S. aureus P . aeruginosa E.
• Example 2 Long Lasting hygiene challenge.
• compositions were used (as is) Comp C (%w) Comp D (%w) Example 2 (%w) Thymol 0.025 0.025 Terpineol 0.05 0.05 Eugenol 0.005 0.005 Poly acrylic acid 1) 0.015 0.015 Poly ethylene oxide 1) 0.01 0.01 Isopropanol 0.65 0.65 Curcuma extract 0.005 0.005 Benzalkonium chloride 0.15 0.15 Citric acid 0.02 0.02 Water Up to 100% Up to 100% Up to 100% 1)
• the polymer complex comprised PAA (poly acrylic acid; Mw 100,000 D, ex Sigma-Aldrich) and PEO (poly ethylene oxide; Mw 100,000 D, ex Sigma-Aldrich), in a total amount as given in the table, or its individual components.
• compositions according to the invention still provides anti-microbial activity to the surface, even though the single ingredients do not show the same effect.
• Example 3 Long Lasting hygiene challenge.
• compositions were used (as is) Comp E (%w) Example 3 (%w) Example 4 2) (%w) Thymol 0.025 0.025 Terpineol 0.05 0.05 Eugenol 0.005 0.005 Poly acrylic acid 1) 0.015 0.015 0.015 Poly ethylene oxide 1) 0.01 0.01 0.01 C12-EO5 Nonionic 0.15 0.15 Benzalkonium chloride 0.15 Citric acid 0.02 0.02 Water Up to 100% Up to 100% Up to 100% 1)
• the polymer complex comprised PAA (poly acrylic acid; Mw 100,000 D, ex Sigma-Aldrich) and PEO (poly ethylene oxide; Mw 100,000 D, ex Sigma-Aldrich), in a total amount as given in the table, or its individual components. 2) Comparative
• compositions according to the invention still provides anti-microbial activity to the surface, even though the single ingredients do not show the same effect.
• the additional benefit of benzalkonium chloride is also demonstrated.

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)
• Health & Medical Sciences (AREA)
• Emergency Medicine (AREA)
• Molecular Biology (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Detergent Compositions (AREA)

Priority Applications (1)

Applications Claiming Priority (3)

Publications (2)

Family

ID=45066199

Family Applications (1)

Country Status (8)

Families Citing this family (16)

Family Cites Families (7)

• 2011
  • 2011-05-17 WO PCT/EP2011/057930 patent/WO2011151169A1/en active Application Filing
  • 2011-05-17 EA EA201201618A patent/EA020708B1/ru not_active IP Right Cessation
  • 2011-05-17 BR BR112012028719-2A patent/BR112012028719B1/pt not_active IP Right Cessation
  • 2011-05-17 EP EP11719579.2A patent/EP2576747B1/en active Active
  • 2011-05-17 CN CN201180026526.1A patent/CN102906237B/zh not_active Expired - Fee Related
  • 2011-05-17 PL PL11719579T patent/PL2576747T3/pl unknown
  • 2011-05-30 AR ARP110101847A patent/AR081502A1/es active IP Right Grant
• 2012
  • 2012-11-08 ZA ZA2012/08409A patent/ZA201208409B/en unknown

Also Published As

Similar Documents

Legal Events