EP1592300A2 - Additiv zur verleihung von bakteriziden und mikrobiziden eigenschaften an materialien - Google Patents

Additiv zur verleihung von bakteriziden und mikrobiziden eigenschaften an materialien

Info

Publication number
EP1592300A2
EP1592300A2 EP04710427A EP04710427A EP1592300A2 EP 1592300 A2 EP1592300 A2 EP 1592300A2 EP 04710427 A EP04710427 A EP 04710427A EP 04710427 A EP04710427 A EP 04710427A EP 1592300 A2 EP1592300 A2 EP 1592300A2
Authority
EP
European Patent Office
Prior art keywords
additive
diphenyl ether
ester
hydroxy diphenyl
fatty acid
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Withdrawn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
EP04710427A
Other languages
English (en)
French (fr)
Inventor
Paul Alexander
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.)
Eradibac Ltd
Original Assignee
Eradibac Ltd
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 Eradibac Ltd filed Critical Eradibac Ltd
Publication of EP1592300A2 publication Critical patent/EP1592300A2/de
Withdrawn legal-status Critical Current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
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
    • A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
    • A01N31/14—Ethers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/14—Paints containing biocides, e.g. fungicides, insecticides or pesticides
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/34—Filling pastes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00—Materials not provided for elsewhere
    • C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
    • 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
    • C11D3/24—Organic compounds containing halogen
    • 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
    • C11D7/28—Organic compounds containing halogen
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2200/00—Chemical nature of materials in mouldable or extrudable form for sealing or packing joints or covers
    • C09K2200/06—Macromolecular organic compounds, e.g. prepolymers
    • C09K2200/0615—Macromolecular organic compounds, e.g. prepolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C09K2200/0625—Polyacrylic esters or derivatives 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
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02—Anionic compounds
    • C11D1/04—Carboxylic acids or salts thereof

Definitions

  • the present invention relates to an improved additive for imparting bactericidal and antimicrobial properties to a material, particularly but not exclusively for use in surface coatings such as paints and sealants.
  • Triclosan or 2,4,4'-trichloro-2'-hydroxy diphenyl ether has been widely used since the 1960's against the spread of microbes.
  • the compound has been incorporated into a range of consumer goods to impart bactericidal properties, including plastics for toys and kitchen utensils, cosmetics and toothpaste.
  • the substance is a potent killer of microbes, such as bacteria and fungi and acts by blocking the active site of an enzyme called enoyl-acyl carrier-protein reductase ("ENR") which prevents the microbe from manufacturing fatty acids required for cell membrane construction and other vital functions. Humans do not possess this enzyme and therefore the compound is harmless to them thereby enabling its incorporation into consumer products as a safe bactericide.
  • ELR enoyl-acyl carrier-protein reductase
  • Triclosan is a powder that is scarcely soluble in water. This limits the application of the compound to certain products.
  • the powder has been provided as a dispersion in paint, but although satisfactory, this paint composition does suffer
  • the Triclosan powder can only be added at certain stages of the manufacturing process.
  • the Triclosan may be distributed unevenly throughout the coating and may subsequently be removed from the surface by cleaning operations, causing paints based on a dispersion of Triclosan powder to experience loss of bactericidal protection over time.
  • attempts to dissolve the triclosan in solvents can give paints an undesirable granular appearance when applied to a surface.
  • a first aspect of the present invention provides an additive for a material, the additive comprising 2,4,4'-trichloro-2'-hydroxy diphenyl ether or a derivative thereof dissolved in a carrier, the carrier comprising at least one selected from the group consisting of a fatty acid, a fatty acid ester, a fatty acid salt, an alkyl ester of benzoic acid, an alkyl ester of a dicarboxylic acid and an ester of glycerol or a derivative of any of the aforesaid.
  • a long chain fatty acid and/or fatty acid ester and/or ester of glycerol is used, including triglycerides.
  • fatty acids or esters having chain lengths of 6 to 20 carbon atoms are used. Branched or straight chain, saturated, unsaturated, or polyunsaturated fatty acids may be used.
  • the fatty acids are saturated.
  • the fatty acids and/or fatty acid esters or salts may be natural or synthetic. Natural or synthetic oils or fats may be used as the source of the fatty acid and/or fatty acid esters or salts. Derivatives may include, for example, ethoxylated fatty acid esters.
  • the carrier for dissolving the 2,4,4'-trichloro-2'-hydroxy diphenyl ether may be one or more compounds selected from the group consisting of linseed oil, mineral oil, castor oil, soya oil, tall oil fatty acids, C ⁇ -C ⁇ 5 alkyl benzoate, MCT oil (medium chain triglycerides), 2-Ethyl Hexyl palmitate, 2-Di-Ethyl Hexyl adipate, triglyceride ester, isodecyl oleate, isopropyl myristate, isopropyl palmitate, isopropyl stearate and butyl myristate.
  • the fatty acid may also be sodium, potassium and amine soaps of, for example, oleic, ricinoleic, coconut and myristic fatty acids.
  • the carrier is selected from the group consisting of at least one C1-C20 alkyl ester of a long chain alkyl or aryl carboxylic acid, including fatty acids, dicarboxylic acids and benzoic acids or a glycerol ester.
  • the carrier for the 2,4,4'-trichloro-2'-hydroxy diphenyl ether is a triglyceride, especially MCT oil, or a fatty acid ester having the general basic formula:
  • R is a branched or straight chain alkyl group having at least 3 carbon atoms; X is 13 to 17 and Y is 27 to 35.
  • R has 3 to 8 carbon atoms.
  • Preferred additives according to the present invention comprise 2,4,4'- trichloro-2'-hydroxy diphenyl ether and a fatty acid ester selected from the group consisting of isopropyl myristate, 2-ethyl-hexyl palmitate, butyl myristate, isopropyl stearate and isopropyl palmitate.
  • the solution preferably contains a maximum of 60% by weight 2,4,4'- trichloro-2'-hydroxy diphenyl ether.
  • the solution contains a minimum of 30% by weight of 2,4,4'-trichloro-2'-hydroxy diphenyl ether, more preferably 30% to 50%, especially 40% by weight.
  • the solution may also contain other minor ingredients, such as dispersants/surface tension modifiers and additional microbiologically active substances (such as 2-n-octyl-4-isothiazolin-3-one).
  • the minor ingredients are in an amount 0 to 10% w/w, or in amount of 0- 30% in the case of microbiologically active substances.
  • the viscosity of the solution is lmPa (0.01 Poise) to 2 Pas (20 Poise).
  • a second aspect of the present invention provides the use of an additive comprising 2,4,4'-trichloro-2'-hydroxy diphenyl ether or derivative thereof dissolved in a carrier, the carrier comprising at least one selected from the group consisting of a fatty acid, a fatty acid ester, a fatty acid salt, an alkyl ester of benzoic acid, an alkyl ester of a dicarboxylic acid and an ester of glycerol or a derivative of any of the
  • aforesaid for imparting bactericidal and/or antimicrobial properties to a material such as a surface coating, particularly a paint formulation.
  • a third aspect of the present invention provides a method for imparting bactericidal and/or antimicrobial properties to a material comprising adding to the material 2,4,4'-trichloro-2'-hydroxy diphenyl ether or derivative thereof dissolved in a carrier, the carrier comprising at least one selected from the group consisting of a fatty acid, a fatty acid ester, a fatty acid salt, an alkyl ester of benzoic acid, an alkyl ester of a dicarboxylic acid and an ester of glycerol or a derivative of any of the aforesaid.
  • the surface coating comprises a paint formulation.
  • a paint composition comprising a binder and a pigment and further comprising 2,4,4'-trichloro-2'- hydroxy diphenyl ether or a derivative thereof dissolved in a carrier, the carrier comprising at least one from the group consisting of a fatty acid, a fatty acid ester, a fatty acid salt, an alkyl ester of benzoic acid, an alkyl ester of a dicarboxylic acid and an ester of glycerol or a derivative of any of the aforesaid.
  • any appropriate binder such as a resin or polymer, may be included in the paint composition as is standard in the art.
  • any pigment may be used, such as titanmm dioxide.
  • the paint composition may also contain solvents, thinners and diluents and may include conventional additives for paints, such as anticorrosive pigments, filler/extender pigments, dispersants, preservatives, tliickening/structuring agents, antifoaming agents, antisettling agents and antiskinning agents.
  • the additive may be incorporated into other surface coatings such as sealants and mastics to impart bactericidal and antimicrobial properties to the coating.
  • the solution may also be added to a cleaning solution.
  • the solution of the 2,4,4'-trichloro-2'-hydroxy diphenyl ether in a carrier as herein described may be added to a surface coating composition during or after manufacture of the coating.
  • the solution of 2,4,4'-trichloro-2'-hydroxy diphenyl ether is present in the material to which it is added at less than 5% by volume, more preferably 0.1 to 2.5%, especially 0.5-1.5 %. It is to be appreciated that a material may be provided in a concentrated form, which is diluted prior to application to a substrate.
  • Example 1 describes the preparation of an additive according to the present invention and its incorporation into a surface coating
  • Examples 2 to 5 provide the compositions of different types of paint formulations provided with the additive of the present invention
  • Example 6 describes a mastic composition provided with the additive of the present invention
  • Example 7 describes a cleaning solution provided with the additive of the present invention
  • Example 8 investigates the bactericidal properties of paint formulations provided with the additive of the present invention, and with reference to the accompanying drawings in which:
  • Figure 1 is a plot of the number of viable bacteria against time (in days) for treated and untreated Paracem Semi-gloss paint.
  • Figure 2 is a plot of the number of viable bacterial against time (in days) for treated and untreated Pegakote 2-pack epoxy paint.
  • Triclosan (2,4,4'-trichloro-2'-hydroxy diphenyl ether) was dissolved in 60% by weight of isopropyl myristate (synonyms include tetradecanoic acid 1-methylethyl ester, estergel, isopropyl tetradecanoate, myristic acid isopropyl ester).
  • This solution was then added to a water-based paint composition in an amount 1-2% by volume.
  • the Triclosan appears to be completely dispersed within the paint composition with no granular appearance.
  • the Triclosan solution of the present invention appears to be adsorbed onto the surface of the paint resin.
  • the paint resin forms a film with the Triclosan forming an integral part of the film. This also suggests that, following scrubbing of the film, a diffusion process will replenish depleted levels of the antimicrobial substance within the surface coating.
  • the solution form of the Triclosan also allows for its addition at any stage of the manufacture of the paint and even post- manufacture, allowing addition of the solution as an additive at or after the point of sale of the paint.
  • Triclosan solution according to the present invention was added to a waterborne 2-pack epoxy finish paint to provide the following composition:
  • Bisphenol A/F liquid epoxy resin (emulsifiable) 24.50 epoxy equivalent (ISO 3001) 177/g/Eq Water 6.75
  • Triclosan solution was added to Component 1 but could have been added to Component 2 to provide a paint composition having the required properties.
  • the triclosan solution replaces water in the standard paint formulation.
  • Triclosan solution according to the present invention was added to a waterborne matt emulsion paint to provide the following composition:
  • Triclosan solution according to the present invention was added to a waterborne gloss emulsion paint to provide a composition having the following formula:
  • the triclosan solution replaces water provided in the basic paint formulation.
  • Example 4 A triclosan solution of the present invention was added to a decorative quality gloss enamel paint for brush application to provide the following composition:
  • the triclosan solution additive replaces white spirit provided in the basic formulation.
  • a triclosan solution of the present invention was incorporated into a quick drying industrial enamel for spray application to provide the following composition: % by weight
  • the triclosan solution of the present invention replaces an equivalent amount of Xylene in the basic enamel formulation.
  • a triclosan solution of the present invention was added a mastic formulation
  • the triclosan solution replaces water in the basic mastic formulation.
  • a concentrated cleaning solution is provided with an additive of the present invention to provide a solution with the following composition:
  • Dispersants/surface tension modifiers 0%- 10% w/w
  • Triclosan solution was incorporated into solvent-borne, solvent-free and water-borne paint formulations at a level of 1% w/w and had no noticeable effect on physical properties.
  • the above tests show that the paint compositions treated with a Triclosan solution according to the present invention exhibit excellent bacteriostatic and bactericidal activity. They prevent/inhibit the growth of micro-organisms, subject to the conditions of the Halo test and organisms used, and also give a higher rate of 'kill' than the untreated products under the conditions of the modified AATCC 100 test.
  • the antimicrobial used is recognised as demonstrating antibacterial activity against a large range of gram+ve bacteria (as tested using Staphylococcus aureus) and gram-ve bacteria.
  • Triclosan has been shown to be effective against, inter alia, the Gram-positive bacteria Bacillus cereus, Clostridium botulinum, Corynebacterium acnes, Diplococcus pnuemoniae, Enterococcus faecalis, Lactobacillus arabinosus, Listeria monocytogenes, Micrococcus luteus and Streptococcus aureus and to be effective against, inter alia, the Gram- negative bacteria Aerobacter aerogenes, Bracella abortus, Escherichia coli, Proteus vulgaris, Pseudomonas aeruginosa, and Salmonella enteritidis. From the results obtained it is reasonable to conclude that good bacteriostatic and bactericidal activity should be exhibited against a large range of bacteria.
  • the solution of the present invention may be added to a wide range of aqueous and non-aqueous paints and other coating materials which are applied to a substrate to impart bactericidal and/or antimicrobial properties to the coating on the substrate.
  • the non- granular texture of the solution results in it being more acceptable for inclusion in surface coatings vis-a-vis the Triclosan compositions of the prior art.
  • the solution may be added to the surface coating at any stage, during or post-manufacture of the additive and/or surface coating.
  • Inhibitory Concentrations 'mic' for any organism and ensures there is plenty spare to diffuse throughout the coating. This results in the bactericidal and/or antimicrobial properties of the coating being maintained throughout its service life.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Plant Pathology (AREA)
  • Pest Control & Pesticides (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
EP04710427A 2003-02-15 2004-02-12 Additiv zur verleihung von bakteriziden und mikrobiziden eigenschaften an materialien Withdrawn EP1592300A2 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0303579A GB2398243B (en) 2003-02-15 2003-02-15 An improved additive for imparting bactericidal and antimicrobial properties to a material
GB0303579 2003-02-15
PCT/GB2004/000567 WO2004071537A2 (en) 2003-02-15 2004-02-12 Additive for imparting bactericidal and antimicrobial properties to a material

Publications (1)

Publication Number Publication Date
EP1592300A2 true EP1592300A2 (de) 2005-11-09

Family

ID=9953140

Family Applications (1)

Application Number Title Priority Date Filing Date
EP04710427A Withdrawn EP1592300A2 (de) 2003-02-15 2004-02-12 Additiv zur verleihung von bakteriziden und mikrobiziden eigenschaften an materialien

Country Status (3)

Country Link
EP (1) EP1592300A2 (de)
GB (1) GB2398243B (de)
WO (1) WO2004071537A2 (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111315858A (zh) * 2017-11-14 2020-06-19 宝洁公司 颗粒状抗微生物衣物洗涤剂组合物

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2386589A1 (de) 2010-04-23 2011-11-16 Centre National de la Recherche Scientifique (C.N.R.S) Neue antimikrobielle Zusammensetzung, Verwendung damit und Herstellung davon
CN104255721B (zh) * 2014-08-29 2016-01-27 北京桑普生物化学技术有限公司 一种含2,4,4′-三氯-2′-羟基二苯醚的防腐杀菌剂组合物及用途
CN107691448B (zh) * 2017-10-18 2020-07-28 万华化学集团股份有限公司 一种环氧大豆油基防霉剂及其制备方法和应用、环氧美缝剂
CN114262535A (zh) * 2022-01-14 2022-04-01 美巢集团股份公司 一种绿色环保持久防霉弱碱性腻子及其制备方法

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL123541C (de) * 1967-04-27
US3947576A (en) * 1973-09-27 1976-03-30 Mortell Company Synergistic biostatic composition
US4098877A (en) * 1975-09-15 1978-07-04 American Cyanamid Company Antimicrobial composition (enhanced activity from combination of phenol and a quaternary compound)
US4683080A (en) * 1984-06-11 1987-07-28 Morton Thiokol, Inc. Microbiocidal compositions comprising an aryl alkanol and a microbiocidal compound dissolved therein
US5531982A (en) * 1987-01-30 1996-07-02 Colgate Palmolive Company Antimicrobial oral composition
US5453275A (en) * 1988-05-05 1995-09-26 Interface, Inc. Biocidal polymeric coating for heat exchanger coils
US4832861A (en) * 1988-05-27 1989-05-23 Lever Brothers Company Soap compositions of enhanced antimicrobial effectiveness
JPH0491023A (ja) * 1990-08-06 1992-03-24 Nippon Nohyaku Co Ltd 徐放性製剤
US5236699A (en) * 1992-06-22 1993-08-17 Libin Barry M Antiplaque mouth rinse
US5532291A (en) * 1995-05-16 1996-07-02 Betco Corporation Coating composition and processes therefor
US6110445A (en) * 1995-06-26 2000-08-29 Colgate-Palmotive Company Oral composition exhibiting improved uptake and retention of antibacterial compounds on dental tissue surfaces
US5700842A (en) * 1995-11-01 1997-12-23 Kimberly-Clark Worldwide, Inc. Methods of incorporating a hydrophobic substance into an aqueous solution
CA2431360A1 (en) * 2000-12-14 2002-06-20 Ciba Specialty Chemicals Holding Inc. Surface-active compositions
KR20030019641A (ko) * 2001-06-01 2003-03-06 아이씨아이 아메리카스 인크. 알콕실화 알칸올 아미드 계면활성제 및 항균화합물의 용액

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111315858A (zh) * 2017-11-14 2020-06-19 宝洁公司 颗粒状抗微生物衣物洗涤剂组合物
CN111315858B (zh) * 2017-11-14 2021-12-24 宝洁公司 颗粒状抗微生物衣物洗涤剂组合物

Also Published As

Publication number Publication date
WO2004071537A3 (en) 2004-10-14
WO2004071537A2 (en) 2004-08-26
GB0303579D0 (en) 2003-03-19
GB2398243B (en) 2005-09-07
GB2398243A (en) 2004-08-18

Similar Documents

Publication Publication Date Title
KR100426888B1 (ko) 캔내 및 건식피복 항미생물제
EP0963291B1 (de) Verfahren zur verhinderung der entfärbung von pyrithion enthaltenden beschichtungszusammensetzungen
JPH09501688A (ja) 抗細菌性および抗汚れ性オキサチアジン類およびそれらの酸化物
CN103102725A (zh) 一种添加茶叶末和茶多酚的涂料及其制备方法
WO2007092632A2 (en) Surface coating compositions and methods
CN1184885C (zh) 1,3－双(羟甲基)－5,5－二甲基乙内酰脲和1,2－苯并异噻唑啉－3－酮的抗微生物混合物
JP2009519207A (ja) 相乗作用を示す銀含有殺生物組成物
US20190071576A1 (en) Use of alkyd resins
CA2636506C (en) Antimicrobial paint
WO2004071537A2 (en) Additive for imparting bactericidal and antimicrobial properties to a material
JP2001509474A (ja) ２−（チオシアノメチルチオ）ベンゾチアゾールとメチレン−ビス（チオシアネート）との混合物をカルボン酸ジメチルアミドとともに含有する相乗的抗微生物組成物
JPWO2015107934A1 (ja) 防腐剤組成物
JP4982837B2 (ja) 海洋付着菌用抗菌剤
RU2186810C2 (ru) Состав с бактерицидными свойствами
JP2010522796A (ja) 組成物
JP4226302B2 (ja) 塗料用抗菌剤
CN109952030A (zh) 涂料和涂饰用的抗微生物剂
JP2011519968A (ja) 防汚塗料用の環境に優しい新規な微生物付着防止剤及び該防止剤を含有する防汚塗料
WO2006131147A1 (en) Wax emulsions to increase biocidal properties in paints
JPS59164704A (ja) 防腐防カビ剤
JP5383969B2 (ja) エマルジョン製剤組成物及び水溶性殺菌剤の安定化方法
WO2018219788A1 (en) Use of natural oil in polymers for disinfecting purposes
US11814532B1 (en) Coatings with antimicrobial copper glass nanoparticles and diol compounds
Strangis et al. EFFICACY OF DEEP EUTECTIC SOLVENTS (DESs) FOR MITIGATING BIODETERIORATION IN CULTURAL HERITAGE: IN SITU EVALUATION.
CA3015726C (en) Use of alkyd resins

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20050816

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LI LU MC NL PT RO SE SI SK TR

AX Request for extension of the european patent

Extension state: AL LT LV MK

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20070315

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20071127