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
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
  • A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2

Definitions

• the present invention relates to storage-stable, synergistic combinations containing glutaric dialdehyde (GDA) and 2-methyl-2H-isothiazol-3-one (methylisothiazolinone, MIT) and optionally 2-bromo-2-nitropropane-l, 3-diol (Bronopol) and / or other active substances for the protection of technical materials.
• GDA glutaric dialdehyde
• MIT 2-methyl-2H-isothiazol-3-one
• Bronopol 2-bromo-2-nitropropane-l, 3-diol
• GDA has been known as an antimicrobial compound since the 1960's (Gorman, SP, Scott, EM and Russel, AD, 1980. Antibacterial activity, uses and mechanism of action of glutaraldehyde, J. Appl. Bacteriol, 48, 161-90. ).
• GDA is used as a 2 to 50% by weight solution adjusted to a pH ⁇ 7. At pH values above 7, GDA shows an increasingly pronounced tendency to polymerise, but also the so-called "fast killing" effect, which is why GDA is often used as a disinfectant and sterilizer, or slimicides, as a preservative becomes.
• MIT is usually treated with other, fast-acting isothiazolinones such as e.g. 5-chloro-2-methyl-4-isothiazolin-3-one (chloromethylisothiazolinone, CMIT) or further combined with bronopol.
• isothiazolinones such as e.g. 5-chloro-2-methyl-4-isothiazolin-3-one (chloromethylisothiazolinone, CMIT) or further combined with bronopol.
• Microbicidal mixtures containing GDA and CMIT and MIT are already known and are used for the preservation of technical materials.
• DE 3313689 describes mixtures comprising GDA and CMIT and MIT, which are used for the antimicrobial treatment of cooling water systems and process waters in papermaking.
• KR 2000015319 A describes synergistic mixtures containing GDA and CMIT and MIT for use in papermaking and for the preservation of process water.
• JP 2002 370906 A describes mixtures comprising GDA and MIT in the ratio of 1: 1 and synergistic mixtures comprising GDA, MIT and o-phthalaidehyde.
• the abovementioned mixtures according to the prior art have in common that they have a very low storage stability due to the formation of decomposition products, which severely restricts the technical applicability or does not fully develop the desired effect.
• JP 03112908 describes stabilized microbicidal solutions containing GDA as well as CMIT and MIT as magnesium complex as well as polyglycols. ⁇ EP2008 / 064095
• JP 05271015 describes mixtures containing GDA and clathrates of CMIT and MIT with 1, 1, 6,6-tetraphenyl-2,4-hexadyn-l, 6-diol.
• Agents comprising GDA, MIT and optionally CMIT, wherein the CMIT content is 0 to 4% based on the weight ratio of CMIT to MIT and the weight ratio of GDA to MIT at least 1.1: 1, preferably 1.5: 1 to 50: 1 is more preferably 2: 1 to 20: 1 and most preferably 4: 1 to 20: 1.
• compositions according to the invention are characterized in that they are highly effective as microbicidal agents and are particularly storage-stable.
• compositions according to the invention are outstandingly suitable as preservatives for industrial materials.
• technical materials generally includes, but is not limited to, the following technical materials and products:
• Starch solutions and syrups or other starch-based products e.g. Printing thickener
• Mineral oils and mineral oil products such as diesel fuels
• the technical materials are preferably:
• Starch solutions and sturries or other starch-based products e.g. Pressure thickeners - slurries of other raw materials such as color pigments (for example iron oxide pigments, carbon black pigments, titanium dioxide pigments) or slurries of inorganic fillers and pigments such as kaolin, calcium carbonate, gypsum, bentonite, magnesium silicates, smectide or talcum.
• color pigments for example iron oxide pigments, carbon black pigments, titanium dioxide pigments
• inorganic fillers and pigments such as kaolin, calcium carbonate, gypsum, bentonite, magnesium silicates, smectide or talcum.
• the technical materials are:
• inorganic fillers and pigments such as kaolin, calcium carbonate, gypsum, bentonite, magnesium silicates, smectite or talc.
• compositions of the invention are used to protect engineering materials as described above; They are particularly effective against bacteria, yeasts and against slime organisms and in the presence of another fungicide additionally against molds.
• the following microorganisms may be mentioned: Altemaria such as Altemaria tenuis, Aspergillus such as Aspergillus niger, Chaetomium such as Chaetomium globosum, Fusarium such as Fusarium solani, Lentinus such as Lentinus tigrinus, Penicillium such as Penicillium glaucum;
• Alcaligenes such as Alcaligenes faecalis, Bacillus such as Bacillus subtilis, Escherichia such as Escherichia coli, Pseudomonas such as Pseudomonas aeruginosa or Pseudomonas fluorescens, Staphylococcus such as Staphylococcus aureus;
• Candida like Candida albicans, Geotrichum like Geotrichum candidum, Rhodotorula like Rhodotorula rubra.
• the agents according to the invention may additionally contain one or more active substances which are selected from the group:
• TMAD 1,
• the agents according to the invention for achieving an additional fungicidal action additionally contain one or more fungicides.
• Preferred fungicides are selected from the group:
• compositions according to the invention may contain between 0 and 4% CMIT, preferably 0 to 2%, more preferably 0 to 1% and most preferably 0 to 0.5%, based on the weight of the amount of MIT also present.
• the sum of GDA and MIT can be varied over a wide range.
• the sum of GDA and MIT is from 1 to 80% by weight, preferably from 2 to 70% by weight and more preferably from 5 to 60% by weight.
• the agents according to the invention are preferably aqueous and may additionally contain polyhydric alcohols to further improve the storage stability.
• Polyhydric alcohols include glycols such as diethylene glycol, triethylene glycol, tetraethylene glycol, polyethylene glycols of 200 to 10,000 molecular weight, dipropylene glycol, tripropylene glycol or polypropylene glycol of 200 to 10,000 molecular weight.
• the proportion of other active ingredients optionally used in the inventive compositions can vary within a wide range and depends strongly on the nature of the active ingredient and the medium to be protected. In general, it may be between 0.2 and 30% by weight, preferably between 0.5 and 25% by weight and more preferably between 1 and 20% by weight.
• the invention also includes the technical materials treated with the agents according to the invention.
• the invention also encompasses a method for antimicrobial finishing of technical materials, which is characterized in that technical materials are treated with an agent according to the invention.
• the invention encompasses the use of GDA and MIT for the preparation of the agents according to the invention, as well as the use of the inventive agents for the protection of industrial materials.
• inventive compositions are characterized by the fact that they are highly effective as microbicidal agents and particularly stable on storage. Examples
• MIC (A) concentration of substance A that inhibits microbial growth
• MIC (B) concentration of substance B that inhibits microbial growth
• MIC (A + B) concentration of substance A + B that inhibits microbial growth
• SI> 1 means antagonism
• Preventol GDA 50 containing 50% glutaric aldehyde
• Kathon 39 FG containing 24.3% of a salt-free mixture of chloromethylisothiazolinone and methylisothiazolinone
• 72.3 g of water were mixed together, stored at 40 ° C. and analyzed analytically after 1 and 2 months, respectively.

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• Life Sciences & Earth Sciences (AREA)
• Agronomy & Crop Science (AREA)
• Pest Control & Pesticides (AREA)
• Plant Pathology (AREA)
• Health & Medical Sciences (AREA)
• Engineering & Computer Science (AREA)
• Dentistry (AREA)
• General Health & Medical Sciences (AREA)
• Wood Science & Technology (AREA)
• Zoology (AREA)
• Environmental Sciences (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)

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• 2007
  • 2007-10-25 DE DE102007051006A patent/DE102007051006A1/de not_active Withdrawn
• 2008
  • 2008-10-20 KR KR1020107011252A patent/KR20100087021A/ko not_active Application Discontinuation
  • 2008-10-20 WO PCT/EP2008/064095 patent/WO2009053325A2/de active Application Filing
  • 2008-10-20 EP EP08841360A patent/EP2205087A2/de not_active Withdrawn
  • 2008-10-20 BR BRPI0818707-0A2A patent/BRPI0818707A2/pt not_active Application Discontinuation
  • 2008-10-20 JP JP2010530415A patent/JP2011500754A/ja active Pending
  • 2008-10-20 CN CN200880116322A patent/CN101868150A/zh active Pending
  • 2008-10-28 US US12/738,938 patent/US20110009462A1/en not_active Abandoned

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