EP1483363A1 - Antibakterielles reinigungstuch - Google Patents
Antibakterielles reinigungstuchInfo
- Publication number
- EP1483363A1 EP1483363A1 EP03709247A EP03709247A EP1483363A1 EP 1483363 A1 EP1483363 A1 EP 1483363A1 EP 03709247 A EP03709247 A EP 03709247A EP 03709247 A EP03709247 A EP 03709247A EP 1483363 A1 EP1483363 A1 EP 1483363A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- cleaning wipe
- oil
- glycol
- ether
- 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.)
- Granted
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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/83—Mixtures of non-ionic with anionic compounds
-
- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/049—Cleaning or scouring pads; Wipes
-
- 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
-
- 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
- C11D3/3726—Polyurethanes
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/143—Sulfonic acid esters
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/146—Sulfuric acid esters
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/74—Carboxylates or sulfonates esters of polyoxyalkylene glycols
Definitions
- the present invention relates to a nonwoven fabric which has been impregnated with a liquid cleaning composition that provides a lasting antibacterial protection of hard surfaces.
- U.S. Patent Nos. 6,183,315 and 6,183,763 teach cleaning compositions containing a proton donating agent and having an acidic pH.
- a cleaning wipe for cleaning and lasting antibacterial protection of hard surfaces such as walls, toilet bowl, bath tub, door handle, tables, counter tops and floors
- a nonwoven fabric containing at least polyester fibers and viscose fibers
- a liquid cleaning composition comprises an anionic surfactant and a polycationic antibacterial agent, a nonionic surfactant, an emulsifier, optionally, a perfume, optionally, a proton donating agent, optionally, cosurfactants and solvents and water
- the liquid cleaning composition is not an emulsion and does not contain proteins, metallic salts, enzymes, amides, sodium hypochlorite, dimethicone, N-methyl-2-pyrrolidone, monoalkyl phosphate or silicon based sulfosuccinate.
- the present invention relates to an antibacterial cleaning wipe for hard surfaces which comprises approximately:
- liquid cleaning composition 70 wt. % to 80 wt. % of a liquid cleaning composition being impregnated in said nonwoven fabric, wherein said liquid cleaning composition comprises:
- n 4 to 6 or from the group consisting of quatemized cationic polymer having the structure of
- composition does not contain potassium sorbate, an alkali metal carbonate, salicylamide substituted compositions, silver ions, an anionic surfactant as crosslinking agent, poly (hexamethylene biguanide) stearate or a cationic surfactant such as a quaternary ammonium compound.
- perfume is used in its ordinary sense to refer to and include any non-water soluble fragrant substance or mixture of substances including natural (i.e., obtained by extraction of flower, herb, blossom or plant), artificial (i.e., mixture of natural oils or oil constituents) and synthetically produced substance) odoriferous substances.
- perfumes are complex mixtures of blends of various organic compounds such as alcohols, aldehydes, ethers, aromatic compounds and varying amounts of essential oils (e.g., terpenes) such as from 0% to 80%, usually from 10% to 70% by weight, the essential oils themselves being volatile odoriferous compounds and also serving to dissolve the other components of the perfume.
- the precise composition of the perfume is of no particular consequence to cleaning performance so long as it meets the criteria of water immiscibility and having a pleasing odor.
- the perfume, as well as all other ingredients should be cosmetically acceptable, i.e., non-toxic, hypoallergenic, etc.
- Suitable essential oils are selected from the group consisting of: Anethole 20/21 natural, Aniseed oil china star, Aniseed oil globe brand,, Balsam (Peru), Basil oil (India), Black pepper oil, Black pepper oleoresin 40/20, Bois de Rose (Brazil) FOB, Borneol Flakes (China), Camphor oil, White, Camphor powder synthetic technical, Cananga oil (Java), Cardamom oil, Cassia oil (China), Cedarwood oil (China) BP,
- the water soluble nonionic surfactants utilized in this invention are commercially well known and include the primary aliphatic alcohol ethoxylates, secondary aliphatic alcohol ethoxylates, alkylphenol ethoxylates and ethylene-oxide-propylene oxide condensates on primary alkanols, such a Plurafacs (BASF) and condensates of ethylene oxide with sorbitan fatty acid esters such as the Tweens (ICI).
- the nonionic synthetic organic detergents generally are the condensation products of an organic aliphatic or alkyl aromatic hydrophobic compound and hydrophilic ethylene oxide groups.
- any hydrophobic compound having a carboxy, hydroxy, amido, or amino group with a free hydrogen attached to the nitrogen can be condensed with ethylene oxide or with the polyhydration product thereof, polyethylene glycol, to form a water-soluble nonionic detergent. Further, the length of the polyethenoxy chain can be adjusted to achieve the desired balance between the hydrophobic and hydrophilic elements.
- the nonionic surfactant class includes the condensation products of a higher alcohol (e.g., an alkanol containing about 8 to 18 carbon atoms in a straight or branched chain configuration) condensed with about 5 to 30 moles of ethylene oxide, for example, lauryl or myristyl alcohol condensed with about 16 moles of ethylene oxide (EO), tridecanol condensed with about 6 to moles of EO, myristyl alcohol condensed with about 10 moles of EO per mole of myristyl alcohol, the condensation product of EO with a cut of coconut fatty alcohol containing a mixture of fatty alcohols with alkyl chains varying from 10 to about 14 carbon atoms in length and wherein the condensate contains either about 6 moles of EO per mole of total alcohol or about 9 moles of EO per mole of alcohol and tallow alcohol ethoxylates containing 6 EO to 11 EO per mole of alcohol.
- a higher alcohol e.g.
- Neodol ethoxylates which are higher aliphatic, primary alcohol containing about 9- 15 carbon atoms, such as Cg-C-
- Additional satisfactory water soluble alcohol ethylene oxide condensates are the condensation products of a secondary aliphatic alcohol containing 8 to 18 carbon atoms in a straight or branched chain configuration condensed with 5 to 30 moles of ethylene oxide.
- Examples of commercially available nonionic detergents of the foregoing type are C11-C15 secondary alkanol condensed with either 9 EO (Tergitol
- nonionic surfactants include the polyethylene oxide condensates of one mole of alkyl phenol containing from about 8 to 18 carbon atoms in a straight- or branched chain alkyl group with about 5 to 30 moles of ethylene oxide.
- alkyl phenol ethoxylates include nonyl phenol condensed with about 9.5 moles of EO per mole of nonyl phenol, dinonyl phenol condensed with about 12 moles of EO per mole of phenol, dinonyl phenol condensed with about 15 moles of EO per mole of phenol and di-isoctylphenol condensed with about 15 moles of EO per mole of phenol.
- nonionic surfactants of this type include Igepal CO-630
- nonionic surfactants are the water-soluble condensation products of a C8-C20 alkanol with a heteric mixture of ethylene oxide and propylene oxide wherein the weight ratio of ethylene oxide to propylene oxide is from 2.5:1 to 4:1 , preferably 2.8:1 to 3.3:1 , with the total of the ethylene oxide and propylene oxide (including the terminal ethanol or propanol group) being from 60-85%, preferably 70-80%, by weight.
- Such detergents are commercially available from BASF-Wyandotte and a particularly preferred detergent is a C-
- C20 alkanoic acid esters having a HLB of 8 to 15 also may be employed as the nonionic detergent ingredient in the described composition.
- These surfactants are well known and are available from Imperial Chemical Industries under the Tween trade name. Suitable surfactants include polyoxyethylene (4) sorbitan monolaurate, polyoxyethylene (4) sorbitan monostearate, polyoxyethylene (20) sorbitan trioleate and polyoxyethylene (20) sorbitan tristearate.
- Other suitable water-soluble nonionic surfactants are marketed under the trade name "Pluronics”. The compounds are formed by condensing ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol.
- the molecular weight of the hydrophobic portion of the molecule is of the order of 950 to 4000 and preferably 200 to 2,500.
- the addition of polyoxyethylene radicals to the hydrophobic portion tends to increase the solubility of the molecule as a whole so as to make the surfactant water-soluble.
- the molecular weight of the block polymers varies from 1 ,000 to 15,000 and the polyethylene oxide content may comprise 20% to 80% by weight.
- these surfactants will be in liquid form and satisfactory surfactants are available as grades L 62 and L 64.
- Suitable water-soluble non-soap, anionic surfactants used in the instant compositions include those surface-active or detergent compounds which contain an organic hydrophobic group containing generally 8 to 26 carbon atoms and preferably 10 to 18 carbon atoms in their molecular structure and at least one water-solubilizing group selected from the group of sulfonate, sulfate and carboxylate so as to form a water-soluble detergent.
- the hydrophobic group will include or comprise a Cs- C22 al . or ac yl group.
- Such surfactants are employed in the form of water-soluble salts and the salt-forming cation usually is selected from the group consisting of sodium, potassium, ammonium, zinc, magnesium and mono-, di- or tri-C2-C3 alkanolammonium, with the sodium, magnesium and ammonium cations again being preferred.
- Suitable sulfonated anionic surfactants are the well known higher alkyl mononuclear aromatic sulfonates such as the higher alkyl benzene sulfonates containing from 10 to 16 carbon atoms in the higher alkyl group in a straight or branched chain, C8-C15 alkyl toluene sulfonates and C8-C15 alkyl phenol sulfonates.
- the linear alkyl benzene sulfonate has a high content of 3- (or higher) phenyl isomers and a correspondingly low content (well below 50%) of 2- (or lower) phenyl isomers, that is, wherein the benzene ring is preferably attached in large part at the 3 or higher (for example, 4, 5, 6 or 7) position of the alkyl group and the content of the isomers in which the benzene ring is attached in the 2 or 1 position is correspondingly low.
- Particularly preferred materials are set forth in U.S. Patent 3,320,174.
- Suitable anionic surfactants are the olefin sulfonates, including long-chain alkene sulfonates, long-chain hydroxyalkane sulfonates or mixtures of alkene sulfonates and hydroxyalkane sulfonates.
- Preferred olefin sulfonates contain from 14 to 16 carbon atoms in the R alkyl group and are obtained by sulfonating an a-olefin.
- Suitable anionic sulfonate surfactants are the paraffin sulfonates containing 10 to 20, preferably 13 to 17, carbon atoms.
- Primary paraffin sulfonates are made by reacting long-chain alpha olefins and bisulfites and paraffin sulfonates having the sulfonate group distributed along the paraffin chain are shown in
- Examples of satisfactory anionic sulfate surfactants are the preferred C8-C18 alkyl sulfate salts and the Cs-Ci ⁇ alkyl sulfate salts and the C8-C18 alkyl ether polyethenoxy sulfate salts having the formula R(OC2H4) n OSO3M wherein n is 1 to 12, preferably 1 to 5, and M is a solubilizing cation selected from the group consisting of sodium, potassium, ammonium, zinc, magnesium and mono-, di- and triethanol ammonium ions.
- the alkyl sulfates may be obtained by sulfating the alcohols obtained by reducing glycerides of coconut oil or tallow or mixtures thereof and neutralizing the resultant product.
- the alkyl ether polyethenoxy sulfates are obtained by sulfating the condensation product of ethylene oxide with a C8-C18 alkanol and neutralizing the resultant product.
- the alkyl sulfates may be obtained by sulfating the alcohols obtained by reducing glycerides of coconut oil or tallow or mixtures thereof and neutralizing the resultant product.
- the alkyl ether polyethenoxy sulfates are obtained by sulfating the condensation product of ethylene oxide with a C8-C18 alkanol and neutralizing the resultant product.
- alkyl ether polyethenoxy sulfates differ from one another in the number of moles of ethylene oxide reacted with one mole of alkanol.
- Preferred alkyl sulfates and preferred alkyl ether polyethenoxy sulfates contain 10 to 16 carbon atoms in the alkyl group.
- the C8-C12 alkylphenyl ether polyethenoxy sulfates containing from 2 to 6 moles of ethylene oxide in the molecule also are suitable for use in the inventive compositions.
- These surfactants can be prepared by reacting an alkyl phenol with 2 to 6 moles of ethylene oxide and sulfating and neutralizing the resultant ethoxylated alkylphenol.
- C9-C15 alkyl ether polyethenoxyl carboxylates having the structural formula R(OC2H4)nOX COOH wherein n is a number from 4 to 12, preferably 5 to 10 and X is selected from the group consisting of CH2, C(0)R1 and wherein Ri is a C1-C3 alkylene group.
- Preferred compounds include C9-C11 alkyl ether polyethenoxy (7-9) C(O) CH2CH2COOH, C13-C15 alkyl ether polyethenoxy (7-9) and C10-C12 alkyl ether polyethenoxy (5-7) CH2COOH.
- These compounds may be prepared by condensing ethylene oxide with appropriate alkanol and reacting this reaction product with chloracetic acid to make the ether carboxylic acids as shown in US Pat. No. 3,741 ,911 or with succinic anhydride or phtalic anhydride.
- anionic detergents will be present either in acid form or salt form depending upon the pH of the final composition, with the salt forming cation being the same as for the other anionic detergents.
- One emulsifier used in the instant composition is LRI manufactured by Wackherr which is a mixture of a PEG-40 hydrogenated Castor oil and PPG-26 buteth 26.
- Other useful emulsifiers are all the surfactants that can be used to solubilize perfumes or other lipophilic ingredients into water as the surfactants belonging to the following families and showing an HLB higher than 12 : the ethoxylated fatty alcohols, ethoxylated lanolin, ethoxylated glycerides or ethoxylated hydroxylated glycerides, ethoxylated amides, ethoxylated carboxylic acids (polyethylene glycol acylates and di- acylates), EO-PO block copolymers or any propoxylated PEO ethers as well as sorbitan and sorbitol esters. More specifically, the following examples can be mentionned :
- the cosurfactants in the instant compositions are selected from the group consisting of polypropylene glycol of the formula HO(CH3CHCH2 ⁇ )nH wherein n is a number from 1 to 18, and mono and di C-
- Representative members of the polypropylene glycol include dipropylene glycol and polypropylene glycol having a molecular weight of 150 to 1000, e.g., polypropylene glycol 400.
- Satisfactory glycol ethers are ethylene glycol monobutyl ether (butyl cellosolve), diethylene glycol monobutyl ether (butyl carbitol), triethylene glycol monobutyl ether, mono, di, tri propylene glycol monobutyl ether, tetraethylene glycol monobutyl ether, mono, di, tripropylene glycol monomethyl ether, propylene glycol monomethyl ether, ethylene glycol monohexyl ether, diethylene glycol monohexyl ether, propylene glycol tertiary butyl ether, ethylene glycol monoethyl ether, ethylene glycol monomethyl ether, ethylene glycol monopropyl ether, ethylene glycol monopentyl ether, diethylene glyco
- the preferred C1-C4 alkanols are ethanol or isopropanol and mixtures thereof.
- the final essential ingredient in the inventive compositions having improved interfacial tension properties is water.
- the proportion of water in the compositions generally is in the range of 20% to 99.7%, preferably 70% to 97% by weight.
- compositions of this invention may often and preferably do contain one or more additional ingredients which serve to improve overall product performance.
- the antibacterial solution of this invention may, if desired, also contain other components either to provide additional effect or to make the product more attractive to the consumer.
- Colors or dyes in amounts up to 0.5% by weight, 2,6-di-tert.butyl-p-cresol, etc., in amounts up to 2% by weight; and pH adjusting agents, such as sulfuric acid, chlorhydric acid or sodium hydroxide, as needed.
- the proton donating agent that can be used in the instant composition is selected from the group consisting of organic acids and inorganic acids and mixtures thereof.
- the organic acids are selected from the group consisting of mono- and di- aliphatic carboxylic acids and hydroxy containing organic acids and mixtures thereof.
- Typical organic acids are adipic acid, succinic acid, lactic acid, glycolic acid, salicylic acid, tartaric acid, citric acid, gluconic acid, malic acid, acetic acid, pyruvic acid, sorbic acid, propionic acid, formic acid and ortho hydroxy benzoic acid.
- Typical inorganic acids are sulfuric acid, nitric acid and hydrochloric acid.
- the cleaning compositions are prepared by simple batch mixing at 25°C-30°C.
- the nonwoven fabric is impregnated with the liquid cleaning composition by means of a positive impregnation process.
- the liquid is positively fed into the nonwoven fabric through a controlled gear pump and injection bar at a ratio of about 2.4 to 2.8 grams of liquid cleaning composition to about 1 gram of the nonwoven fabric.
- the nonwoven fabric is formed from 10 wt. % to 90 wt. % of viscose fibers and 10 wt. % to 90 wt. % of polyester fibers such as Spunlace made by the Dexter Corporation. More preferably the nonwoven fabric comprises 10 wt. % to 95 wt. % of wood pulp fibers, 1 wt.
- Such a nonwoven fabric which is manufactured by Dexter Corporation under the name Hydraspun comprises about 60% to 95% of wood pulp fabrics, 2.5 wt. % to 20 wt. % of viscose fibers and 2.5 wt. % to 20 wt. % of polyester fibers.
- the cleaning wipes were made following the aforementioned process.
- Ceramic tiles are treated with the product, let dried and rinsed with sterile tap water. After drying, the surface is inoculated with a germ suspension containing Bovin Serum Albumin at 3g/l as interfering substance. After 1 hour contact, the remaining living germs are quantified. 3 inoculations are successively performed at 1 hour interval.
- the performance of the product is expressed in terms of Iog10 'CFU' reduction versus an untreated tile.
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)
- Cleaning Implements For Floors, Carpets, Furniture, Walls, And The Like (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/081,279 US6475976B1 (en) | 2002-02-22 | 2002-02-22 | Antibacterial cleaning wipe comprising polyhexamethylene-4-biguanide hydrochloride |
US81279 | 2002-02-22 | ||
US277962 | 2002-10-22 | ||
US10/277,962 US6596681B1 (en) | 2002-02-22 | 2002-10-22 | Antibacterial cleaning wipe |
PCT/US2003/005321 WO2003072696A1 (en) | 2002-02-22 | 2003-02-20 | Antibacterial cleaning wipe |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1483363A1 true EP1483363A1 (de) | 2004-12-08 |
EP1483363B1 EP1483363B1 (de) | 2006-11-29 |
Family
ID=27767329
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP03709247A Expired - Lifetime EP1483363B1 (de) | 2002-02-22 | 2003-02-20 | Antibakterielles reinigungstuch |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP1483363B1 (de) |
AT (1) | ATE346908T1 (de) |
AU (1) | AU2003213201A1 (de) |
DE (1) | DE60310042T2 (de) |
DK (1) | DK1483363T3 (de) |
ES (1) | ES2276046T3 (de) |
WO (1) | WO2003072696A1 (de) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2061454B1 (de) * | 2006-09-08 | 2018-06-06 | DeLaval Holding AB | Zusammensetzungen mit einer c2-c14-carboxylsäure und einem tensid zur behandlung von huferkrankungen |
JP2013537430A (ja) * | 2010-08-27 | 2013-10-03 | アニトックス コーポレーション | 抗菌性処方剤 |
CN102246794B (zh) * | 2011-06-08 | 2015-08-19 | 江中药业股份有限公司 | 一种杀灭微生物的组合物 |
CN102246793B (zh) * | 2011-06-08 | 2015-08-19 | 江中药业股份有限公司 | 一种杀灭微生物的组合物及其应用 |
JP5904873B2 (ja) * | 2012-05-23 | 2016-04-20 | 旭化成ホームプロダクツ株式会社 | 水拭き用洗浄剤組成物 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK0823937T3 (da) * | 1995-05-05 | 1999-12-27 | Procter & Gamble | Glasrensningssammensætninger med lineært alkylsulfatoverfladeaktive midler |
US5962388A (en) * | 1997-11-26 | 1999-10-05 | The Procter & Gamble Company | Acidic aqueous cleaning compositions |
WO1999040791A1 (en) * | 1998-02-12 | 1999-08-19 | Surfacine Development Company, Llc | Disinfectant compositions providing sustained biocidal action |
US6653274B1 (en) * | 1999-09-27 | 2003-11-25 | The Proctor & Gamble Company | Detergent composition comprising a soil entrainment system |
EP1146112A1 (de) * | 2000-04-14 | 2001-10-17 | The Procter & Gamble Company | Verfahren zur Reinigung und/oder Desinfektion von einer harten Oberfläche unter Verwendung einer Zusammensetzung enthaltend ein Biguanid als antimikrobieller Wirkstoff |
-
2003
- 2003-02-20 AT AT03709247T patent/ATE346908T1/de not_active IP Right Cessation
- 2003-02-20 DE DE60310042T patent/DE60310042T2/de not_active Expired - Fee Related
- 2003-02-20 AU AU2003213201A patent/AU2003213201A1/en not_active Abandoned
- 2003-02-20 DK DK03709247T patent/DK1483363T3/da active
- 2003-02-20 WO PCT/US2003/005321 patent/WO2003072696A1/en active IP Right Grant
- 2003-02-20 EP EP03709247A patent/EP1483363B1/de not_active Expired - Lifetime
- 2003-02-20 ES ES03709247T patent/ES2276046T3/es not_active Expired - Lifetime
Non-Patent Citations (1)
Title |
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See references of WO03072696A1 * |
Also Published As
Publication number | Publication date |
---|---|
EP1483363B1 (de) | 2006-11-29 |
AU2003213201A1 (en) | 2003-09-09 |
DE60310042D1 (de) | 2007-01-11 |
ATE346908T1 (de) | 2006-12-15 |
WO2003072696A1 (en) | 2003-09-04 |
DE60310042T2 (de) | 2007-06-28 |
ES2276046T3 (es) | 2007-06-16 |
DK1483363T3 (da) | 2007-04-02 |
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