WO2008080184A2 - Verwendung von polymeren guanidinen zum bekämpfen von mikroorganismen - Google Patents
Verwendung von polymeren guanidinen zum bekämpfen von mikroorganismen Download PDFInfo
- Publication number
- WO2008080184A2 WO2008080184A2 PCT/AT2007/000589 AT2007000589W WO2008080184A2 WO 2008080184 A2 WO2008080184 A2 WO 2008080184A2 AT 2007000589 W AT2007000589 W AT 2007000589W WO 2008080184 A2 WO2008080184 A2 WO 2008080184A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- polymeric
- diamine
- polymeric guanidinium
- guanidinium hydroxide
- hydroxide
- Prior art date
Links
Classifications
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
- A01N47/42—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides containing —N=CX2 groups, e.g. isothiourea
- A01N47/44—Guanidine; Derivatives thereof
Definitions
- the present invention relates to the use of polymeric guanidines for controlling microorganisms.
- Biocidal polymers based on guanidinium hydrochloride, in particular their activity against Escherichia coli Bakte ⁇ en are already known (see, WO 01/85676). Furthermore, it is already known that such guanidine derivatives can be used as fungicidal agents (see WO 2006/047800).
- the present invention provides a use which solves the problem at least in some aspects, since it has now surprisingly been found that polymeric guanidinium hydroxides can be used particularly well for controlling unwanted microorganisms such as bacteria, yeasts and fungi.
- a preferred embodiment of the guanidinium hydroxides which can be used according to the invention are based on a diamine which contains oxyalkylene chains and / or alkylene groups between two amino groups, and is particularly preferably obtainable by polyethers. condensation of a guanidine acid addition salt with the diamine to obtain a polycondensation product in salt form, which is then converted into the hydroxide form by basic anion exchange.
- the salts which can be used as starting materials for this embodiment of the guanidinium hydroxides which can be used according to the invention are known, in particular the hydrochlorides (cf., WO 01/85676).
- a further preferred embodiment of the polymeric guanidinium hydroxide poly [2- (2-ethoxy-ethoxyethyl) -guanidinium hydroxide] which can be used according to the invention having an average molecular weight of about 1000 is obtained by reacting 4.43 mol of guanidinium hydrochloride in 4.03 mol of triethylene glycol diamine at 50 0 C dissolves. The mixture is then heated to 120 ° C and stirred for 2 hours at this temperature.
- the temperature is maintained for 2 hours, then a vacuum (0.1 bar) applied and stirred for 2 more hours under vacuum at 170 ° C. It is then vented to atmospheric pressure, allowed to cool to 120 ° C and diluted with demineralized water to about 50%. With phosphoric acid is neutralized to a pH of about 6, allowed to cool and diluted to the desired concentration.
- the hydroxide form is prepared by treating the previously obtained solution with a strongly alkaline anion exchanger in hydroxide form, conveniently in an exchange column (eg "Ambersep 900 OH" or "Lewatit MP 500").
- a strongly alkaline anion exchanger in hydroxide form conveniently in an exchange column (eg "Ambersep 900 OH" or "Lewatit MP 500").
- a further preferred embodiment of the guanidinium hydroxide which can be used according to the invention consists in that, as representatives of the series of polyoxyalkylene-guanidine salts, those using triethylene glycol diamine (relative molecular mass: 148), of polyoxypropylene diamine (relative molecular mass: 230) and of Polyoxyethylenediamine (relative molecular mass: 600), or of polyhexamethylenediamine (relative molecular mass: be obtained.
- a further preferred embodiment of the guanidinium hydroxides which can be used according to the invention is characterized in that as the polymeric guanidine derivative poly (2- (2-ethoxyethoxyethyl) guanidinium hydroxide) having at least 3 guanidinium radicals is contained.
- polymeric guanidine derivative poly (2- (2-ethoxyethoxyethyl) guanidinium hydroxide) having at least 3 guanidinium radicals is contained.
- diamine is an alkylene diamine of the general formula
- H 2 N- (CH 2 ) - NH 2 is provided, in which n is an integer between 2 and 10, in particular 6.
- oxyalkylenediamine is a compound of the general formula
- the average molecular mass of the guanidinium hydroxide which can be used according to the invention is preferably in the range from 500 to 3,000, particularly preferably in the range from 500 to 2,000, very particularly preferably in the range from 500 to 1,500. Further preferred is an average molecular mass of 1000.
- Preferred uses of the polymeric guanidinium hydroxide are as a misting agent for microbial decontamination; Decontamination of building fabric; as a preservative for detergents and cleaners; as a preservative for paints and varnishes; as a preservative for cosmetics: as an antimicrobial additive in natural and synthetic polymers and leather, wherein the synthetic polymers are preferably formed as fibers or films or as a coating material; as a slime control agent in papermaking and petroleum production; and as an additive for cooling lubricant;
- Cooling lubricants are used in the machining of metals.
- "Machining” is understood to mean all mechanical machining processes in which the metal is shaped to the desired shape by removing it in the form of chips.
- the machining techniques include, for example, turning, drilling, milling and loops. These activities are usually performed with a lathe or a drill.
- the function of the cooling lubricant is that it reduces both the friction between the metallic workpiece and the tool, whereby the wear of the tool is reduced, as well as the heating of the material counteracts. At temperatures above 1000 ° C, cooling lubricants allow higher processing speeds. But the cooling lubricant can also serve to rinse the chips out of the field and to protect the metallic workpiece from corrosion.
- cooling lubricants There are e.g. non-water miscible mineral oils with or without additives, which additives may be fatty acids or sulfur and phosphorus containing organic compounds. Furthermore, milky white mineral oil-containing oil-in-water emulsions are known. Mineral oil-free solutions, in turn, are transparent and contain sodium carbonate or nitrite in water.
- additives serve substances that bring an added benefit with their chemical properties, such as. Antirust, higher lubricity in extreme conditions, preventing foaming or inhibiting the growth of bacteria, yeasts and fungi in the emulsion.
- the guanidinium hydroxide used is preferably poly [2- (2-ethoxyethoxyethyl) guanidinium hydroxide] having an average molecular weight of about 1000 (AI), an average molecular weight of about 1500 (A-2).
- an average molecular weight of about 500 (A-3), an average molecular weight of about 2,000 (A-4), an average molecular weight of about 2,500 (A-5), or an average molecular weight of about 3,000 (A-6), as well as in addition, a polycondensate of poly (hexamethylene-guanidirdum hydroxide) and poly [2- (2-ethoxy) -ethoxyethyl) -guanidinium hydroxide] in a molar ratio of 3: 1 (A-7).
- the agents according to the invention can be used as such or depending on their respective physical and / or chemical properties in the form of their formulations or the application examples prepared therefrom, such as aerosols, capsule suspensions, cold mist concentrates. heat-fog concentrates, encapsulated granules, fine granules, flowable concentrates for the treatment of microbially contaminated material, ready-to-use solutions, dustable powders, emulsifiable concentrates, oil-in-water emulsions, water-in-oil emulsions, macrogranules, microgranules, oil-dispersible Powders, oil-miscible flowable concentrates, oil-miscible liquids, foams, pastes, pesticide-coated seeds, suspension concentrates, suspension-emulsion concentrates, soluble concentrates, suspensions, wettable powders, soluble powders, dusts and granules, water-soluble granules or tablets, water-soluble powders and wettable ones
- This example is intended to document the superiority of the OH form of the polymeric guanidine over the Chlo ⁇ d form.
- MIC minimal inhibitory concentration, determined by microdilution method
- this modification significantly improves the environmental compatibility of the products, as chloride increases the solubility of heavy metals in groundwater, salts the soil and forms hydrochloric acid in the case of thermal disposal or fire.
- the effectiveness as a pot preservative was tested, for example, in a mineral interior wall paint by adding 0.2 to 2% by weight of the guanidine derivative with germinated tap water, with a complete germ killing being detectable from 1%.
- the color samples were diluted 1:10 (vol., Part color: vol., Part water) with contaminated tap water. 100 ⁇ l of this dilution were spread on TSA plates (bacterial culture medium), incubated for 24 hours at 35 ° C. and then the total germ count in the form of colony-forming units (CFU) was counted.
- the subject guanidine derivatives are also known as Preservative for cosmetics and even for direct application to the skin as a disinfectant suitable.
- polymeric guanidine hydroxides which can be used according to the invention are soluble in water and can be applied with conventional nebulizer devices in the form of very fine droplets, virtually as an active substance mist in enclosed spaces, for ambient air and surface sterilization.
- This fogging application enables rapid control of bacteria, fungi and viruses. It can treat all contaminated premises, such as mold contaminated homes, air conditioners, germinated food production facilities, livestock farming areas, as well as public facilities (hospitals, spas, schools) quickly and effectively. For effective treatment, the premises to be treated should be closed.
- the active substance eliminates not only pathogens but also airborne, unpleasant odors.
- the active ingredient adheres to all particles and surfaces or walls during the nebulization phase and thus also forms a preventive, sustained effective protective film.
- the invention thus also relates to the decontamination by means of nebulization of the polymeric guanidine derivative in apartments, air conditioning and ventilation shafts, hotels and catering areas, food and pharmaceutical production facilities, storage and transport facilities especially ships and cars, livestock housing areas, laboratories and also public facilities such as hospitals, spas Areas and schools.
- the amount of active ingredient used is optimized to a required minimum.
- the procedure and the type of nebulizer are adapted to the application area and room size.
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2007339730A AU2007339730A1 (en) | 2006-12-29 | 2007-12-28 | Use of polymeric guanidines for controlling microorganisms |
CA002676461A CA2676461A1 (en) | 2006-12-29 | 2007-12-28 | Use of polymeric guanidines for controlling microorganisms |
EP07845311A EP2114164B1 (de) | 2006-12-29 | 2007-12-28 | Verwendung von polymeren guanidinen zum bekämpfen von mikroorganismen |
US12/523,845 US20100303752A1 (en) | 2006-12-29 | 2007-12-28 | Use of polymeric guanidines for controlling microorganisms |
DE502007004609T DE502007004609D1 (de) | 2006-12-29 | 2007-12-28 | Verwendung von polymeren guanidinen zum bekämpfen von mikroorganismen |
EA200970652A EA200970652A1 (ru) | 2006-12-29 | 2007-12-28 | Применение полимерных гуанидинов для борьбы с микроорганизмами |
AT07845311T ATE475313T1 (de) | 2006-12-29 | 2007-12-28 | Verwendung von polymeren guanidinen zum bekämpfen von mikroorganismen |
HK10104448.8A HK1138155A1 (en) | 2006-12-29 | 2010-05-06 | Use of polymeric guanidines for controlling microorganisms |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT0215606A AT504675A1 (de) | 2006-12-29 | 2006-12-29 | Polymere guanidinderivate |
ATA2156/2006 | 2006-12-29 | ||
EP07150147.2 | 2007-12-19 | ||
EP07150147A EP2071954A1 (de) | 2007-12-19 | 2007-12-19 | Verwendung von polymeren Guanidin-Derivaten zum Bekämpfen von unerwünschten Mikro-organismen im Pflanzenschutz |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2008080184A2 true WO2008080184A2 (de) | 2008-07-10 |
WO2008080184A3 WO2008080184A3 (de) | 2008-10-02 |
Family
ID=39133882
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/AT2007/000589 WO2008080184A2 (de) | 2006-12-29 | 2007-12-28 | Verwendung von polymeren guanidinen zum bekämpfen von mikroorganismen |
Country Status (10)
Country | Link |
---|---|
US (1) | US20100303752A1 (de) |
EP (1) | EP2114164B1 (de) |
KR (1) | KR20090119840A (de) |
AT (1) | ATE475313T1 (de) |
AU (1) | AU2007339730A1 (de) |
CA (1) | CA2676461A1 (de) |
DE (1) | DE502007004609D1 (de) |
EA (1) | EA200970652A1 (de) |
HK (1) | HK1138155A1 (de) |
WO (1) | WO2008080184A2 (de) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009092123A2 (de) * | 2008-01-24 | 2009-07-30 | Aka Central Research Laboratories Gmbh | Verfahren zur bekämpfung unerwünschter mikroorganismen an bananenpflanzen |
EP2230258A1 (de) | 2009-03-18 | 2010-09-22 | Mindinvest Holdings Ltd. | Mikrobiozid wirkendes Arzneimittel |
DE102009052725A1 (de) * | 2009-11-12 | 2011-05-19 | B. Braun Melsungen Ag | Verwendung von Polyoxyalkylendiamin-basierten Polyguanidinderivaten für medizinische Artikel |
EP2338923A1 (de) | 2009-12-24 | 2011-06-29 | Sebastian Oberwalder | Polyurethan mit einem bioziden Polyharnstoff als Comonomer |
EP2338342A1 (de) | 2009-12-24 | 2011-06-29 | Sebastian Oberwalder | Polyharnstoff mit bioziden Eigenschaften |
WO2012041910A1 (de) * | 2010-10-01 | 2012-04-05 | Elektra Management S.R.O. | Lösung von guanidinium-verbindungen, verfahren unter einsatz dieser lösung sowie deren verwendung |
CN102665778A (zh) * | 2009-11-12 | 2012-09-12 | B·布朗·梅尔松根有限公司 | 用于医用制品的聚合活性组分或低聚活性组分的应用 |
WO2013064161A1 (de) | 2011-11-02 | 2013-05-10 | Mindinvest Holdings Ltd. | Polyguanidinsilikat und dessen verwendung |
WO2015071063A1 (de) | 2013-11-18 | 2015-05-21 | Evonik Industries Ag | Verwendung von guanidinumsetzungsprodukten bei der herstellung von polyurethansystemen |
EP3459983A1 (de) | 2017-09-25 | 2019-03-27 | Evonik Degussa GmbH | Herstellung von polyurethansystemen |
EP3524055A1 (de) | 2018-02-08 | 2019-08-14 | BCSK Biocid GmbH | Antibakterielles und spermizides gleitmittel |
EP3886823A4 (de) * | 2018-11-30 | 2022-07-06 | UCAR Health GmbH | Maske, wundauflage, slip, bh, taschentuch, kissen, pad, wegwerfbares chirurgisches kleidungsstück, wegwerftücher mit antimikrobiellen eigenschaften aus gewebe, vlies, baumwolle, vlies-baumwoll-gemischtem polyethylen und polypropylen und polystyrol |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110804179A (zh) * | 2019-11-19 | 2020-02-18 | 石家庄学院 | 具有良好成膜特性和长期抑菌性的高分子离子液体及其应用 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3475375A (en) * | 1967-06-23 | 1969-10-28 | Du Pont | Novel amorphous guanidine silicates,and compositions thereof with synthetic resins |
EP0472093A1 (de) * | 1990-08-22 | 1992-02-26 | BASF Aktiengesellschaft | Bis-Guanidine und diese enthaltende Fungizide |
WO2001085676A1 (de) * | 2000-05-11 | 2001-11-15 | P.O.C. Oil Industry Technology Beratungsges.M.B.H | Biozide polymere auf der basis von guanidin-salzen |
WO2006047800A1 (de) * | 2004-11-05 | 2006-05-11 | Oskar Schmidt | Biozid, insbesondere fungizid wirkendes mittel |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2007770A (en) * | 1930-09-01 | 1935-07-09 | Anticoman G M B H | Polymethylenediguanidine compounds and process of making said compounds |
US2325586A (en) * | 1940-03-21 | 1943-08-03 | Du Pont | Polymeric guanidines and process for preparing the same |
-
2007
- 2007-12-28 EP EP07845311A patent/EP2114164B1/de not_active Revoked
- 2007-12-28 US US12/523,845 patent/US20100303752A1/en not_active Abandoned
- 2007-12-28 AU AU2007339730A patent/AU2007339730A1/en not_active Abandoned
- 2007-12-28 DE DE502007004609T patent/DE502007004609D1/de active Active
- 2007-12-28 KR KR1020097015665A patent/KR20090119840A/ko not_active Application Discontinuation
- 2007-12-28 EA EA200970652A patent/EA200970652A1/ru unknown
- 2007-12-28 AT AT07845311T patent/ATE475313T1/de active
- 2007-12-28 WO PCT/AT2007/000589 patent/WO2008080184A2/de active Application Filing
- 2007-12-28 CA CA002676461A patent/CA2676461A1/en not_active Abandoned
-
2010
- 2010-05-06 HK HK10104448.8A patent/HK1138155A1/xx not_active IP Right Cessation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3475375A (en) * | 1967-06-23 | 1969-10-28 | Du Pont | Novel amorphous guanidine silicates,and compositions thereof with synthetic resins |
EP0472093A1 (de) * | 1990-08-22 | 1992-02-26 | BASF Aktiengesellschaft | Bis-Guanidine und diese enthaltende Fungizide |
WO2001085676A1 (de) * | 2000-05-11 | 2001-11-15 | P.O.C. Oil Industry Technology Beratungsges.M.B.H | Biozide polymere auf der basis von guanidin-salzen |
WO2006047800A1 (de) * | 2004-11-05 | 2006-05-11 | Oskar Schmidt | Biozid, insbesondere fungizid wirkendes mittel |
Non-Patent Citations (1)
Title |
---|
ALBERT MARTIN ET AL: "Structure-activity relationships of oligoguanidines: Influence of counterion, diamine, and average molecular weight on biocidal activities." BIOMACROMOLECULES, Bd. 4, Nr. 6, November 2003 (2003-11), Seiten 1811-1817, XP002490825 ISSN: 1525-7797 * |
Cited By (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009092123A2 (de) * | 2008-01-24 | 2009-07-30 | Aka Central Research Laboratories Gmbh | Verfahren zur bekämpfung unerwünschter mikroorganismen an bananenpflanzen |
EP2084967A1 (de) * | 2008-01-24 | 2009-08-05 | Aka Central Research Laboratories GmbH | Verfahren zur Bekämpfung unerwünschter Mikroorganismen an Bananenpflanzen |
WO2009092123A3 (de) * | 2008-01-24 | 2010-04-22 | Aka Central Research Laboratories Gmbh | Verfahren zur bekämpfung unerwünschter mikroorganismen an bananenpflanzen |
EP2230258A1 (de) | 2009-03-18 | 2010-09-22 | Mindinvest Holdings Ltd. | Mikrobiozid wirkendes Arzneimittel |
WO2010106006A1 (de) | 2009-03-18 | 2010-09-23 | Mindinvest Holdings Ltd. | Mikrobiozid wirkendes arzneimittel |
WO2010106007A1 (de) | 2009-03-18 | 2010-09-23 | Mindinvest Holdings Ltd. | Komplex enthaltend ein polymeres guanidin |
CN102665778A (zh) * | 2009-11-12 | 2012-09-12 | B·布朗·梅尔松根有限公司 | 用于医用制品的聚合活性组分或低聚活性组分的应用 |
US9572913B2 (en) | 2009-11-12 | 2017-02-21 | B. Braun Melsungen Ag | Use of polymeric or oligomeric active ingredients for medical articles |
CN102665778B (zh) * | 2009-11-12 | 2016-08-31 | B·布朗·梅尔松根有限公司 | 用于医用制品的聚合活性组分或低聚活性组分的应用 |
US20120283664A1 (en) * | 2009-11-12 | 2012-11-08 | B. Braun Melsungen Ag | Use of Polyoxyalkylene Diamine-Based Polyguanidine Derivatives for Medical Articles |
DE102009052725A1 (de) * | 2009-11-12 | 2011-05-19 | B. Braun Melsungen Ag | Verwendung von Polyoxyalkylendiamin-basierten Polyguanidinderivaten für medizinische Artikel |
EP2338342A1 (de) | 2009-12-24 | 2011-06-29 | Sebastian Oberwalder | Polyharnstoff mit bioziden Eigenschaften |
EP2338923A1 (de) | 2009-12-24 | 2011-06-29 | Sebastian Oberwalder | Polyurethan mit einem bioziden Polyharnstoff als Comonomer |
WO2012041910A1 (de) * | 2010-10-01 | 2012-04-05 | Elektra Management S.R.O. | Lösung von guanidinium-verbindungen, verfahren unter einsatz dieser lösung sowie deren verwendung |
WO2013064161A1 (de) | 2011-11-02 | 2013-05-10 | Mindinvest Holdings Ltd. | Polyguanidinsilikat und dessen verwendung |
WO2015071063A1 (de) | 2013-11-18 | 2015-05-21 | Evonik Industries Ag | Verwendung von guanidinumsetzungsprodukten bei der herstellung von polyurethansystemen |
DE102013223444A1 (de) | 2013-11-18 | 2015-05-21 | Evonik Industries Ag | Verwendung von Guanidinumsetzungsprodukten bei der Herstellung von Polyurethansystemen |
EP3459983A1 (de) | 2017-09-25 | 2019-03-27 | Evonik Degussa GmbH | Herstellung von polyurethansystemen |
EP3524055A1 (de) | 2018-02-08 | 2019-08-14 | BCSK Biocid GmbH | Antibakterielles und spermizides gleitmittel |
WO2019154983A1 (de) | 2018-02-08 | 2019-08-15 | Bcsk Biocid Gmbh | Antibakterielles und spermizides gleitmittel |
EP3886823A4 (de) * | 2018-11-30 | 2022-07-06 | UCAR Health GmbH | Maske, wundauflage, slip, bh, taschentuch, kissen, pad, wegwerfbares chirurgisches kleidungsstück, wegwerftücher mit antimikrobiellen eigenschaften aus gewebe, vlies, baumwolle, vlies-baumwoll-gemischtem polyethylen und polypropylen und polystyrol |
Also Published As
Publication number | Publication date |
---|---|
EA200970652A1 (ru) | 2010-04-30 |
HK1138155A1 (en) | 2010-08-20 |
US20100303752A1 (en) | 2010-12-02 |
EP2114164A2 (de) | 2009-11-11 |
WO2008080184A3 (de) | 2008-10-02 |
CA2676461A1 (en) | 2008-07-10 |
ATE475313T1 (de) | 2010-08-15 |
KR20090119840A (ko) | 2009-11-20 |
DE502007004609D1 (de) | 2010-09-09 |
AU2007339730A1 (en) | 2008-07-10 |
EP2114164B1 (de) | 2010-07-28 |
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