WO2008132060A1 - 2-thiazol-4yl-1h-benzoimidazol (thiabendazol oder tbz) haltige wirkstoff-formulierungen zur herstellung von wpc - Google Patents
2-thiazol-4yl-1h-benzoimidazol (thiabendazol oder tbz) haltige wirkstoff-formulierungen zur herstellung von wpc Download PDFInfo
- Publication number
- WO2008132060A1 WO2008132060A1 PCT/EP2008/054661 EP2008054661W WO2008132060A1 WO 2008132060 A1 WO2008132060 A1 WO 2008132060A1 EP 2008054661 W EP2008054661 W EP 2008054661W WO 2008132060 A1 WO2008132060 A1 WO 2008132060A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- tbz
- wood
- less
- biocidal
- wpc
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/08—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing solids as carriers or diluents
- A01N25/10—Macromolecular compounds
-
- 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
- A01N47/08—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 one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
-
- 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
- A01N43/74—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 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
Definitions
- the present invention relates to the use of biocidal mixtures containing thiabendazole (TBZ) and 3-iodo-2-propynyl-N-butylcarbamate (IPBC) for the protection of
- WPC wood plastic composites
- compositions described which have a borate content (measured as B 2 O 3 ) of less than 0.1 wt .-% and corresponding WPC and their preparation.
- WPC wood plastic composites
- wood-causing and moderately and mildly rot-causing fungi such as e.g. Asco and Deuteromycetes
- wood-destroying fungi such as e.g. Basidiomycetes attacking and destroying WPC.
- WPCs are also capable of absorbing sufficient amounts of water for fungal growth (W. Wang and JJ Morell, Forest Products Journal, 2005, 54 (12), 209-212), so that in addition to the superficial infestation also a risk of deeper layers of the composite material is assumed.
- the fungicide most commonly used today in WPC is zinc borate (J. Simonsen et al., Holzaba, 2004, 58, 205-208), which, however, has a number of disadvantages.
- zinc borate has a higher activity against wood-destroying fungi than against the surface-affecting mold and blue fungus.
- zinc borate shows pronounced leaching due to its water solubility. As a result, are for
- IPBC itself (US-A-2006/0229381) as well as in connection with stabilizers (US Pat.
- TBZ thiabendazole
- the invention therefore relates to the use of a biocidal composition containing TBZ for the protection of wood-plastic composites (WPC) containing thermoplastic polymer and wood particles from infestation and / or destruction by microorganisms, characterized in that the biocidal composition comprises a borate Anteii (measured as B 2 O 3 ) of less than 0.1 wt .-%, preferably less than 0.05 wt%, insbondere less than 0.01 wt .-%.
- WPC wood-plastic composites
- the borate content is preferably determined by atomic absorption spectroscopy (AAS).
- wood particles are understood as meaning, for example, wood fibers, wood granules, wood flour or any other particulate wood pulp
- the hoiz particles preferably have a particle size of less than 3 mm, in particular less than 1.5 mm, particularly preferably less than 1 mm.
- thermoplastic polymer is preferably meant PVC, PET, fluoropolymers, HDPE, LDPE, LLDPE, PP, HDPP, LDPP, WHMWPE, MPE or mixtures thereof.
- biocidal composition may also be used in combinations with other fungicides
- Wood destroying basidiomycetes and / or insecticides and / or algicides are used.
- Examples of effective fungicides against wood-destroying basidiomycetes include: azaconazole, azocyclotin, bitertanol, bromuconazole, cyproconazole, diclobutrazole, difenoconazole, diniconazole, epoxyconazole, etaconazole, fenbuconazole, fenchlorazole,
- Fenethanil fluquinconazole, flusiiazole, flutriafol, furconazole, hexaconazole, imibenconazos, ipconazo ⁇ , isozofos, mycobutanil, metconazole, paclobutrazole, penconazole, propioconazole, prothioconazole, simeoconazole, (+) - cis-1- (4-chloro-phenyl) -2- (1H -l, 2,4-triazol-1-yl) -cycloheptanol, 2- (1-tert-butyl) -1- (2-chlorophenyl) -3- (1, 2,4-triazol-1-yl ) -propan-2-ol, tebuconazole, Tetraconazole, triadimefon, triadimol, triapenthenol, triflumizole, triticonazole, uniconazole and their metal
- algicides examples include: acetochlor, Aciffuorfen, acionifen, acrolein, aiachlor, alloxydim, ametryn, amidosulfuron, amitrole, ammonium sulfamate, anilofos, asulam, atrazine, azafenidine, aziptrotryn, azimsulfuron,
- MCPA MCPA hydrazide, MCPA-ihioethyl, MCPB, mecoprop, mecoprop-P, mefenacet, mefluidide, mesosuifuron, metam, metamifop, metamitron, metazachlor, methabenzthiazuron, methazole, methopyrone, methyl dymron, methylisothiocyanate, metobromuron, metoxurori, metribuzin, metsulfuron , Molinate, Monalid, Monolinuron, MSMA, Metolachlor, Metosulam, Metobenzuron,
- the algicides are triazine compounds, such as terbutryn, cybutryn, propazi ⁇ or terbutone, urea compounds such as diuron, benzthiazuron, methabenzthiazuron, tebutthiuron, and
- Isoproturon or uracils such as terbacil.
- insecticidal active ingredients are, for example, in question.
- Organo (thio) phosphates such as Acephate, Azamethiphos, Azinphos-methyl, Chlorpyrifos, Chlorpyriphos-methyl, Chlorfenvinphos, Diazinon, Dichlorvos, Dicrotophos, Dimethoate, Disulfoton, Ethion, Fenitrothion, Fenthion, Isoxathione, MaSathion, Methami dophos, Methidathion, Methyl- Parathion, mevinphos, monocrotophos, oxydemeton-methyl, paraoxon, parathion, phenthoate, phosalone, phosmet, phosphamidone, phorate, phoxim,
- Carbamates such as alanycarb, benfuracarb, bendiocarb, carbary !, carbosulfan, fenoxycarb, furathiocarb, indoxacarb, methiocarb, methomyl, oxamyl, pirimicarb, propoxur, thiodicarb, triazamates;
- Pyrethroids such as allethrin, bifenthrin, cyfluthrin, cyphenothrin, cypermethrin such as the alpha, beta, theta and zeta isomers, deitamethrin, esfenvalerate, ethofenprox, fenpropathrin, fenvalerate, cyhalothrin, lambda-cyhalothrin, imiprothrin, permethrin, prallethrin, pyrethrin I, pyrethrin II, silafluofen, tau fluvalinate, tefluthrin, tetramethrin, tralomethrin, transfluthrin, zeta-cypermethrin;
- Arthropod growth regulators such as a) chitin synthesis inhibitors; z. B.
- Benzoylureas such as chlorofiuazuron, cyromacin, diflubenzuron, flucycioxuron, fluphenoxuron, hexaflumuron, lufenuron, novaluron, teflubenzuron, tritlumuron; Buprofezin, diofenolan, hexythiazox, etoxazole, clofentazine; b) ecdysone antagonists such as halofenozides, methoxyfenozides, tebufenozides; c) juvenoids such as pyriproxyfen, methoprene, fenoxycarb; d) lipid biosynthesis inhibitors such as spirodicofen;
- Neonicotinoids such as flonicamid, clothianidin, dinotefuran, imidaciopride, thiamethoxam, nhenpyram, nithiazine, acetamiprid, thiaciopride;
- Pyrazole insecticides such as acetoprole, ethiprole, fipronil, tebufenpyrad, tolfenpyrad and vaniliprole. Furthermore Abamectin, Acequinocyi, Amitraz, Azadirachtin, Bifenazate, Cartap, ChlorFenapyr, Chlordimeform, Cyromazine, Diafenthiuron, Diofenolan, Emamec tin, Endosulfan, Fenazaquin, Formetanate, Formetanate hydrochloride, Hydramethylnon, Indoxacarb, Piperonylbutoxid, Pyridaben, Pymetrozine, Spinosad, Thiamethoxam, Thiocyclam, pyrldalyl, fluacyprim, milbemectin, spiro-soap, flupyrazofos, NCS 12,
- insecticides which are effective against wood-destroying insects and in particular against the following wood-destroying insects:
- Lyctidae such as Lyctus linearis, Lyctus brunneus; Bostrichidae such as Dinoderus minutus; Anoblidae such as Anoblum punctatum, Xestoblum rufovillosum; Lymexylida, such as Lymexylon navale; Platypodidae such as Piatypus cylindrus; Oedemeridae like Nacerda melanura.
- Hymenoptera Formicidae such as Camponotus abdominalis, Laslus flavus, Lasius brunneus, Laslus fuliginosus;
- Calotermitidae such as Calotermes flavicollis, Cryptothermes brevis
- Hodotermitidae such as Zootermopsis angusticollis, Zootermopsis nevadensis
- Rhinotermitidae such as Reticulitermes flavipes, Reticulitermes lucifugus, Coptoteres with formosanus, Coptotermes acinaciformis
- Mastotermitidae such as Mastotermes darwiniensis.
- insecticidal active substances from the class of pyrethroids, arthropod growth regulators, such as chitin biosynthesis inhibitors, ecdysone antagonists, juvenoids, lipid biosynthesis inhibitors, neonicotinoids, pyrazole insecticides and chlorfenapyr.
- arthropod growth regulators such as chitin biosynthesis inhibitors, ecdysone antagonists, juvenoids, lipid biosynthesis inhibitors, neonicotinoids, pyrazole insecticides and chlorfenapyr.
- insecticidal active ingredients of the group of neonicotinoids and pyrethroids and very particularly preferably insecticidal active compounds of the group
- the biocidal composition used in the invention contains a release agent.
- a preferred release agent is at least one selected from the group of polymers (fluoropolymers, HDPE, LDPE, LLDPE, PP, HDPP, LDPP, WHMWPE, MPE), alkaline earth metal stearates, metalisifers, pyrogenic silicas and Zn stearate, containing up to 3 wt .-%, preferably up to 2.5 wt .-% and most preferably up to 2 wt .-%, based on the biocidal composition.
- biocidal composition consists of more than 90% by weight, preferably more than 95% by weight, of TBZ and, if appropriate, further biocidal active substances and release agents.
- biocidal composition consists of more than 90 wt .-%, preferably more than 95 wt .-% of TBZ and separating agent.
- the biocidal composition additionally contains a conductivity improver (eg graphite) with a content of up to 5 wt.%, Preferably with a content of up to 3 wt.% And most preferably with a content contains up to 2.5 wt .-%.
- a conductivity improver eg graphite
- the biocidal composition used is preferably present as a particulate solid preparation or in the form of a solution or dispersion of the biocidal composition in a polymer matrix (hereinafter masterbatch).
- the particulate solid preparation can be present as powder or granules. Preferably, it is in a free-flowing form.
- Solid preparation preferably has a particle size of not more than 500 ⁇ m, preferably less than 100 ⁇ m, very particularly preferably less than 50 ⁇ m.
- the solid preparation preferably has an average particle size, determined from the mass distribution, of 50 to 5,000 ⁇ m, preferably 100 to 2,000 ⁇ m, in particular 100 to 500 ⁇ m.
- the solid preparations preferably used, in particular the release agent-containing, are themselves likewise an object of the invention. These are further characterized in that they have a borate content (measured as B 2 O 3 ) of less than 0.1% by weight, in particular less than 0.05 wt .-%.
- the masterbatch is preferably characterized by a polymer, preferably one selected from the group PVC, PET, fluoropolymer, HDPE, LDPE, LLDPE, PP, HDPP, LDPP, WHMWPE, MPE or a mixture thereof and TBZ, optionally separating agents and optionally further Active ingredients and optionally further additives, wherein the masterbatches have a borate content (measured as B 2 O 3 ) of less than 0.1% by weight, in particular less than 0.05% by weight.
- a polymer preferably one selected from the group PVC, PET, fluoropolymer, HDPE, LDPE, LLDPE, PP, HDPP, LDPP, WHMWPE, MPE or a mixture thereof and TBZ, optionally separating agents and optionally further Active ingredients and optionally further additives, wherein the masterbatches have a borate content (measured as B 2 O 3 ) of less than 0.1% by weight, in particular less than 0.05% by weight.
- the masterbatch itself is also the subject of the invention and preferably contains from 20 to 99% by weight of polymer, in particular 40 to 70% by weight and 1 to 80% by weight of TBZ, in particular 30 to 60% by weight.
- the invention further relates to a process for the preparation of the invention
- a masterbatch characterized in that a) a polymer and a biocidal composition comprising TBZ are mixed and extruded together or
- Mixture separates, preferably by distillation.
- the route a) is preferably achieved by compounding and extruding biocidal compositions, for example the above-described solid preparations in polymers such as, for example, PET, PVC, fluoropolymers, HDPE, LDPE, LLDPE, PP, HDPP, LDPP, WHMWPE, MPE and mixtures thereof
- the containing active ingredients preferably have a content of up to 60 wt .-%, preferably of up to 50 wt .-%, in particular of up to 40 wt .-%, based on the masterbatch.
- the route b) is preferably carried out by incorporating solutions of the biocidal compositions, in particular the above-described solid preparations in pre-swollen polymers such as, for example, PET, PVC, fluoropolymers, HDPE, LDPE, LLDPE, PP,
- HDPP high density polyethylene
- LDPP low density polyethylene
- WHMWPE high density polyethylene
- MPE low density polyethylene
- the invention further relates to a method for producing a wood-plastic
- WPC Wood particles, a thermopiastic polymer and a biocidal composition containing TBZ mixed under thermal energy, in particular extruded or injection molded, characterized in that the Composed composition a borate content (measured as B 2 Oj) of less than 0.1 wt .-%, in particular less than 0.05 wt .-%, in particular less than 0.01 Gcw .-%
- thermoplastic polymer For the production of wood-plastic composites, the two-stage processes derived from plastics technology are preferably used. Here are preferably initially granules of thermoplastic polymer, wood and various
- Additives as described above e.g., pigments, coupling agents, etc.
- Additives as described above e.g., pigments, coupling agents, etc.
- Additives as described above e.g. the use of heating-cooling mixers and then to the actual moldings, e.g. by extrusion or injection molding, processed.
- the temperatures usually used for the thermoplastic polymers used are preferably from 120 to 300 ° C. in the case of thermal mixing, in particular extrusion or injection molding.
- biocidal composition can take place within the scope of different production steps of a WPC.
- the biocidal compositions are used in the context of the compounding of wood particles and thermoplastic polymer, e.g. in the heating-cooling mixer, added.
- the biocidal compositions are compounded prior to compounding of wood particles, e.g. Wood fibers and thermoplastic polymer mixed with the wood fibers or the wood granules or the wood flour or mixed with the fPunstoffgranulat before the compounding of wood particles and thermoplastic polymer.
- wood particles e.g. Wood fibers and thermoplastic polymer mixed with the wood fibers or the wood granules or the wood flour or mixed with the fPunstoffgranulat before the compounding of wood particles and thermoplastic polymer.
- the biocidal compositions are prepared by use of suitable solvents and formulation adjuvants, e.g. Emulsifiers, in solutions, emulsions, suspensions or suspoemulsions transferred and treated with these to be compounded with the thermoplastic polymer wood particles, e.g. by spraying or soaking and if necessary dried.
- suitable solvents and formulation adjuvants e.g. Emulsifiers
- thermoplastic polymer eg, PE, PP, PET, HDPE, HDPP, PVC
- WPC wood-plastic composites
- the invention further relates to wood-plastic composites (WPC) containing thermoplastic polymer and wood particles, characterized in that it contains TBZ and a borate content (measured as B 2 O 3 ) of less than 0.1 wt .-%, in particular less than 0.05 wt .-%, in particular less than 0.01 wt .-%.
- the WPCs of the invention may contain, in addition to wood particles, thermoplastic polymer and the TBZ, further additives, e.g. from the group of adhesion promoters, lubricants, UV stabilizers, antioxidants, pigments, flame retardants, conductivity improvers, plastic stabilizers containing, of course, the above proviso regarding the borate content applies.
- the invention further relates to the use of a biocidal mixture containing IPBC and TBZ for the protection of wood-plastic composites (WPC) containing thermoplastic polymer and wood particles against attack and / or destruction by microorganisms.
- WPC wood-plastic composites
- this use is characterized in that the biocidal mixture the
- the biocidal mixture contains a release agent.
- the details of the release agent, which have already been made for the biocidal composition are also valid here. It is preferred if the biocidal mixture consists of more than 90% by weight, preferably more than 95% by weight, of IPBC, TBZ and, if appropriate, further biocidal active substances and release agents.
- the biocidal mixture consists of more than 90 wt .-%, preferably more than 95 wt .-% of IPBC, TBZ and release agent. Furthermore, the use of a biocidal mixture which has a borate content (measured as B 2 O 3 ) of less than 0.1% by volume, in particular less than 0.05% by weight, in particular less than 0.01% by weight, is preferred. % having.
- the biocidal mixture may also be used in combinations with other fungicides against wood-destroying basidiomycetes and / or insecticides and / or algicides. As such, those already mentioned above come into question.
- the biocidal mixture additionally comprises a conductivity improver (eg graphite) with a content of up to 5 wt .-%, preferably with a content of up to 3 wt .-% and most preferably with a content contains up to 2.5 wt .-%.
- a conductivity improver eg graphite
- the biocidal mixture used is preferably in the form of a particulate solid preparation or in the form of a solution or dispersion of the biocidal mixture in a polymer matrix (masterbatch in the following).
- the particulate solid preparation can be present as powder or granules. Preferably, it is present in a freely flowable form.
- Solid preparation preferably has a particle size of not more than 500 ⁇ m, preferably less than 100 ⁇ m, very particularly preferably less than 50 ⁇ m.
- the solid preparation preferably has an average particle size, determined from the mass distribution, of 50 to 5,000 ⁇ m, preferably 100 to 2,000 ⁇ m, in particular 100 to 500 ⁇ m.
- the masterbatch is preferably characterized by a polymer, preferably one selected from the group consisting of PVC, PET, fluoropolymer, HDPE, LDPE, LLDPE, PP, HDPP,
- LDPP 5 WHMWPE, MPE or a mixture thereof and TBZ if appropriate, separating agents and, if appropriate, further active ingredients and optionally further additives.
- the masterbatch itself is also the subject of the invention and preferably contains from 20 to 99% by weight of polymer, in particular 40 to 70% by weight and 1 to 80% by weight of TBZ and IPBC, in particular 30 to 60% by weight.
- the invention further relates to a process for the preparation of the masterbatch according to the invention, which comprises mixing a) the polymer and a biocidal mixture containing TBZ and IPBC and extruding them together or
- the invention further relates to a method for producing a wood-plastic
- WPC Wood particles, a thermoplastic polymer and a biocidal mixture containing TBZ and IPBC, mixed under thermal energy, in particular extruded or injection molded.
- thermoplastic polymer for the production of wood-plastic composites, the two-stage processes derived from plastics technology are preferably used.
- first, granules of thermoplastic polymer, wood and various additives e.g., pigments, coupling agents, etc.
- additives e.g., pigments, coupling agents, etc.
- the invention further relates to wood-plastic composites (WPC) containing thermoplastic polymer and wood particles, characterized in that it contains TBZ and IPBC.
- WPC wood-plastic composites
- % Data means% by weight.
- the vaccine used had the following germs: Penicülium funiculosum, Chaetomium giobosum, Gliocladium virens, Paecilomyces variotii and Aspergillus näger.
- Formulation 1 49.25% TBZ, 49.25% IPBC and 1.5% fumed silica.
- Formulation 2 32.8% TBZ, 65.7% IPBC and 1.5% fumed silica.
- Formulation 1 98.5% TBZ, and 0.5% MG Stearate and 1% Fumed Silica.
- Penicillium funiculosum After testing, resistance to the following germs was tested: Penicillium funiculosum, Chaetomium globosum, GHocladium virens, Paecilomyces variotii and Aspergillus niger.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Abstract
Description
Claims
Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08736324.8A EP2144500B1 (de) | 2007-04-27 | 2008-04-17 | 2-thiazol-4yl-1h-benzoimidazol (thiabendazol oder tbz) haltige wirkstoff-formulierungen zur herstellung von wpc |
CN200880022100A CN101686663A (zh) | 2007-04-27 | 2008-04-17 | 用于生产wpc的含有2-噻唑-4-基-1h-苯并咪唑(噻苯达唑或tbz)的活性物质的配制品 |
US12/597,241 US20100330185A1 (en) | 2007-04-27 | 2008-04-17 | Active ingredient formulations containing 2-thiazole-4yl-1h-benzoimidazol (thiaben-dazole or tbz) for the production of wpc |
BRPI0810681-9A2A BRPI0810681A2 (pt) | 2007-04-27 | 2008-04-17 | Formulações de substâncias ativas contendo 2-tiazol-4il-lh-benzoimidazol (tiabendazol ou tbz) para a produção de wpc (wood plastic composites - compostos plásticos-madeira) |
NZ580665A NZ580665A (en) | 2007-04-27 | 2008-04-17 | Active ingredient formulations containing 2-thiazole-4yl-1h-benzoimidazol (thiabendazole or tbz) for the production of wpc |
MX2009011542A MX2009011542A (es) | 2007-04-27 | 2008-04-17 | Formulaciones de sustancias activas que contienen 2-tiazol-4il-1h-benzoinidazol (tiabendazol o tbz) para la fabricacion de compuestos de madera y plastico. |
AU2008244387A AU2008244387B2 (en) | 2007-04-27 | 2008-04-17 | Active ingredient formulations containing 2-thiazole-4yl-1H-benzoimidazol (thiabendazole or TBZ) for the production of WPC |
ES08736324.8T ES2620742T3 (es) | 2007-04-27 | 2008-04-17 | Formulaciones de principio activo que contienen 2-tiazol-4il-1H-benzoimidazol (tiabendazol o TBZ) para la fabricación de WPC |
JP2010504640A JP5080639B2 (ja) | 2007-04-27 | 2008-04-17 | Wpcを製造するための、2−チアゾール−4−イル−1h−ベンゾイミダゾール(チアベンダゾールまたはtbz)を含む活性成分配合物 |
CA2685011A CA2685011C (en) | 2007-04-27 | 2008-04-17 | Active substance formulations containing 2-thiazol-4-yl-1h-benzoimidazole (thiabendazole or tbz) for the production of wpc |
ZA2009/07521A ZA200907521B (en) | 2007-04-27 | 2009-10-27 | Active ingredient formulations containing 2-thiazole-4yl-1h-benzoimidazol (thiabendazole or tbz) for the production of wpc |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102007020450A DE102007020450A1 (de) | 2007-04-27 | 2007-04-27 | Wirkstoff-Formulierungen zur Herstellung von WPC mit antifungischen Eigenschaften sowie WPC mit antifungischen Eigenschaften |
DE102007020450.9 | 2007-04-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2008132060A1 true WO2008132060A1 (de) | 2008-11-06 |
Family
ID=39591826
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2008/054661 WO2008132060A1 (de) | 2007-04-27 | 2008-04-17 | 2-thiazol-4yl-1h-benzoimidazol (thiabendazol oder tbz) haltige wirkstoff-formulierungen zur herstellung von wpc |
Country Status (15)
Country | Link |
---|---|
US (1) | US20100330185A1 (de) |
EP (1) | EP2144500B1 (de) |
JP (1) | JP5080639B2 (de) |
KR (1) | KR101151184B1 (de) |
CN (1) | CN101686663A (de) |
AU (1) | AU2008244387B2 (de) |
BR (1) | BRPI0810681A2 (de) |
CA (1) | CA2685011C (de) |
DE (1) | DE102007020450A1 (de) |
ES (1) | ES2620742T3 (de) |
MX (1) | MX2009011542A (de) |
NZ (1) | NZ580665A (de) |
RU (1) | RU2461193C2 (de) |
WO (1) | WO2008132060A1 (de) |
ZA (1) | ZA200907521B (de) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1615756A1 (de) * | 2003-04-23 | 2006-01-18 | Ciba SC Holding AG | Verbundwerkstoffe aus natürlichen produkten |
WO2017137157A1 (de) | 2016-02-12 | 2017-08-17 | Thor Gmbh | 2-n-octylisothiazolin-3-on und 4,5-dichlor-2-n-octylisothiazolin-3-on haltige zusammensetzung zur herstellung von wpc |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102009057206B3 (de) * | 2009-11-27 | 2011-09-01 | Technische Universität Dresden | Lignozelluloser Faserwerkstoff, naturfaserverstärkter Kunststoff und Verfahren zur Herstellung |
JP5529833B2 (ja) * | 2010-12-22 | 2014-06-25 | ダウ グローバル テクノロジーズ エルエルシー | グリホサート化合物とdmitsとの相乗的組み合わせ |
JP5529831B2 (ja) * | 2010-12-22 | 2014-06-25 | ダウ グローバル テクノロジーズ エルエルシー | グリホサート化合物とipbcとの相乗的組み合わせ |
JP5511093B2 (ja) * | 2010-12-22 | 2014-06-04 | ダウ グローバル テクノロジーズ エルエルシー | グリホサート化合物とtbzとの相乗的組み合わせ |
AT12874U1 (de) * | 2011-11-30 | 2013-01-15 | Extruwood Gmbh | Verbundprofil aus holz und holzfaserverstärktem kunststoff und verwendung eines derartigen profils |
PL2831160T3 (pl) | 2012-03-28 | 2016-09-30 | Stabilne kompozycje tiabendazolu i fungicydów zawierających jod | |
CN103351632B (zh) * | 2013-06-20 | 2016-04-20 | 黄山华塑新材料科技有限公司 | 一种防白蚁型木塑复合材料及其制备工艺 |
PL418134A1 (pl) | 2016-07-29 | 2018-02-12 | 3 Spare Spółka Z Ograniczoną Odpowiedzialnością | WPC zawierający pył z płyty wiórowej, sposób jego wytwarzania i zastosowanie |
WO2018126276A1 (en) * | 2017-01-01 | 2018-07-05 | Advanced Environmental Recycling Technologies, Inc. | Methods for coating composite articles |
JP6524433B2 (ja) * | 2017-06-07 | 2019-06-05 | 住化エンバイロメンタルサイエンス株式会社 | 木材用抗菌組成物 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06143205A (ja) * | 1992-11-04 | 1994-05-24 | Aica Kogyo Co Ltd | 防かび性木質材の製法 |
WO2004094120A1 (en) * | 2003-04-23 | 2004-11-04 | Ciba Specialty Chemicals Holding Inc. | Natural products composites |
KR20050082946A (ko) * | 2004-02-20 | 2005-08-24 | 송민영 | 목재 방부ㆍ방미를 위한 목재 보존제 조성물 |
US20060013833A1 (en) * | 2004-07-16 | 2006-01-19 | Isp Investments Inc. | Thermal stabilization of biocides in matrix compositions processed at elevated temperatures |
US20060229381A1 (en) * | 2005-04-07 | 2006-10-12 | Isp Investments Inc. | Free-flowing composition of a biocide and a processing additive therewith for incorporation into a polymer or plastic matrix product |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6197204A (ja) * | 1984-10-15 | 1986-05-15 | Takeda Chem Ind Ltd | 工業用殺菌組成物 |
US5939087A (en) * | 1995-03-14 | 1999-08-17 | Hagiwara Research Corporation | Antimicrobial polymer composition |
DE10040814A1 (de) * | 2000-08-21 | 2002-03-07 | Thor Gmbh | Synergistische Biozidzusammensetzung |
US20040076847A1 (en) | 2002-10-17 | 2004-04-22 | Saunders Howard E. | Colored wood/polymer composites |
IL153812A0 (en) | 2003-01-06 | 2003-07-31 | Bromine Compounds Ltd | Improved wood-plastic composites |
US20050049224A1 (en) | 2003-08-29 | 2005-03-03 | Gaglani Kamlesh D. | Antimicrobial mixtures comprising iodopropynyl compounds and dimethyldithiocarbamate derivatives |
US20060013847A1 (en) | 2004-07-16 | 2006-01-19 | Isp Investments Inc. | Thermal stabilization of IPBC biocide |
AU2006251504B2 (en) | 2005-05-22 | 2011-08-11 | U.S. Borax Inc. | Co-biocidal formulation for polymeric materials |
-
2007
- 2007-04-27 DE DE102007020450A patent/DE102007020450A1/de not_active Withdrawn
-
2008
- 2008-04-17 ES ES08736324.8T patent/ES2620742T3/es active Active
- 2008-04-17 JP JP2010504640A patent/JP5080639B2/ja active Active
- 2008-04-17 KR KR1020097024640A patent/KR101151184B1/ko active IP Right Grant
- 2008-04-17 US US12/597,241 patent/US20100330185A1/en not_active Abandoned
- 2008-04-17 RU RU2009143732/13A patent/RU2461193C2/ru not_active IP Right Cessation
- 2008-04-17 BR BRPI0810681-9A2A patent/BRPI0810681A2/pt not_active Application Discontinuation
- 2008-04-17 CA CA2685011A patent/CA2685011C/en active Active
- 2008-04-17 MX MX2009011542A patent/MX2009011542A/es active IP Right Grant
- 2008-04-17 EP EP08736324.8A patent/EP2144500B1/de active Active
- 2008-04-17 CN CN200880022100A patent/CN101686663A/zh active Pending
- 2008-04-17 WO PCT/EP2008/054661 patent/WO2008132060A1/de active Application Filing
- 2008-04-17 AU AU2008244387A patent/AU2008244387B2/en not_active Ceased
- 2008-04-17 NZ NZ580665A patent/NZ580665A/en not_active IP Right Cessation
-
2009
- 2009-10-27 ZA ZA2009/07521A patent/ZA200907521B/en unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06143205A (ja) * | 1992-11-04 | 1994-05-24 | Aica Kogyo Co Ltd | 防かび性木質材の製法 |
WO2004094120A1 (en) * | 2003-04-23 | 2004-11-04 | Ciba Specialty Chemicals Holding Inc. | Natural products composites |
KR20050082946A (ko) * | 2004-02-20 | 2005-08-24 | 송민영 | 목재 방부ㆍ방미를 위한 목재 보존제 조성물 |
US20060013833A1 (en) * | 2004-07-16 | 2006-01-19 | Isp Investments Inc. | Thermal stabilization of biocides in matrix compositions processed at elevated temperatures |
US20060229381A1 (en) * | 2005-04-07 | 2006-10-12 | Isp Investments Inc. | Free-flowing composition of a biocide and a processing additive therewith for incorporation into a polymer or plastic matrix product |
Non-Patent Citations (2)
Title |
---|
DATABASE WPI Week 199425, Derwent World Patents Index; AN 1994-205595, XP002489028 * |
DATABASE WPI Week 200674, Derwent World Patents Index; AN 2006-713964, XP002489107 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1615756A1 (de) * | 2003-04-23 | 2006-01-18 | Ciba SC Holding AG | Verbundwerkstoffe aus natürlichen produkten |
WO2017137157A1 (de) | 2016-02-12 | 2017-08-17 | Thor Gmbh | 2-n-octylisothiazolin-3-on und 4,5-dichlor-2-n-octylisothiazolin-3-on haltige zusammensetzung zur herstellung von wpc |
Also Published As
Publication number | Publication date |
---|---|
CA2685011C (en) | 2013-06-11 |
US20100330185A1 (en) | 2010-12-30 |
KR101151184B1 (ko) | 2012-06-08 |
MX2009011542A (es) | 2009-11-11 |
AU2008244387B2 (en) | 2011-09-29 |
RU2461193C2 (ru) | 2012-09-20 |
DE102007020450A1 (de) | 2008-10-30 |
EP2144500B1 (de) | 2017-02-22 |
CA2685011A1 (en) | 2008-11-06 |
KR20100007919A (ko) | 2010-01-22 |
JP2010525011A (ja) | 2010-07-22 |
RU2009143732A (ru) | 2011-06-10 |
BRPI0810681A2 (pt) | 2014-10-07 |
JP5080639B2 (ja) | 2012-11-21 |
AU2008244387A1 (en) | 2008-11-06 |
EP2144500A1 (de) | 2010-01-20 |
CN101686663A (zh) | 2010-03-31 |
ES2620742T3 (es) | 2017-06-29 |
NZ580665A (en) | 2012-01-12 |
ZA200907521B (en) | 2011-06-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2144500B1 (de) | 2-thiazol-4yl-1h-benzoimidazol (thiabendazol oder tbz) haltige wirkstoff-formulierungen zur herstellung von wpc | |
EP1671542B1 (de) | Synergistische Biozidzusammensetzung mit Pyrithion und Octylisothiazolinonen | |
JP7075451B2 (ja) | 種子処理としての5-フルオロ-4-イミノ-3-(アルキル/置換アルキル)-1-(アリールスルホニル)-3,4-ジヒドロピリミジン-2(1h)-オン | |
EP3042562B1 (de) | Penflufen enthaltende zusammensetzungen | |
EP1776010B1 (de) | Verfahren zur herstellung wässriger wirkstoffzusammensetzungen von in wasser schwer löslichen wirkstoffen | |
DE60003295T2 (de) | Pestizide und/oder pflanzenwachstumsregulierende zusammensetzungen | |
EP2216092B1 (de) | Emulsionszusammensetzung und agrochemische emulsionszusammensetzung | |
AU2008267882B2 (en) | Particulate polymers comprising biocidal active substance | |
US20120071324A1 (en) | Biocidal substances | |
EP2266397A1 (de) | Amidoalkylaminhaltige Azol-Zusammensetzungen für den Schutz technischer Materialien | |
WO2006122657A1 (de) | Verwendung von prochloraz für den holzschutz | |
EP2723169B1 (de) | Mischungen aus treibmittelhaltigen polymeren, insektiziden und wachsen | |
JP5280994B2 (ja) | 農園芸用殺菌粉剤組成物 | |
WO2007031198A1 (de) | Verwendung von triclosan für den holzschutz | |
WO2017137157A1 (de) | 2-n-octylisothiazolin-3-on und 4,5-dichlor-2-n-octylisothiazolin-3-on haltige zusammensetzung zur herstellung von wpc | |
WO2007031199A1 (de) | Verwendung von diclosan für den holzschutz |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200880022100.7 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 08736324 Country of ref document: EP Kind code of ref document: A1 |
|
REEP | Request for entry into the european phase |
Ref document number: 2008736324 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2008736324 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2685011 Country of ref document: CA |
|
WWE | Wipo information: entry into national phase |
Ref document number: 580665 Country of ref document: NZ |
|
WWE | Wipo information: entry into national phase |
Ref document number: MX/A/2009/011542 Country of ref document: MX |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2008244387 Country of ref document: AU Ref document number: 2010504640 Country of ref document: JP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
ENP | Entry into the national phase |
Ref document number: 2008244387 Country of ref document: AU Date of ref document: 20080417 Kind code of ref document: A |
|
ENP | Entry into the national phase |
Ref document number: 20097024640 Country of ref document: KR Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2009143732 Country of ref document: RU |
|
WWE | Wipo information: entry into national phase |
Ref document number: 12597241 Country of ref document: US |
|
ENP | Entry into the national phase |
Ref document number: PI0810681 Country of ref document: BR Kind code of ref document: A2 Effective date: 20091027 |