DD292172A5 - Mittel oder konzentrat zum konservieren von holz oder holzwerkstoffen - Google Patents
Mittel oder konzentrat zum konservieren von holz oder holzwerkstoffen Download PDFInfo
- Publication number
- DD292172A5 DD292172A5 DD90338232A DD33823290A DD292172A5 DD 292172 A5 DD292172 A5 DD 292172A5 DD 90338232 A DD90338232 A DD 90338232A DD 33823290 A DD33823290 A DD 33823290A DD 292172 A5 DD292172 A5 DD 292172A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- mass
- solvent
- parts
- hydroxy
- agent
- Prior art date
Links
- 239000012141 concentrate Substances 0.000 title claims abstract description 31
- 239000002023 wood Substances 0.000 title claims abstract description 25
- 239000000463 material Substances 0.000 title claims abstract description 11
- 239000002904 solvent Substances 0.000 claims abstract description 54
- 239000000126 substance Substances 0.000 claims abstract description 43
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 31
- 239000000203 mixture Substances 0.000 claims abstract description 23
- 239000011230 binding agent Substances 0.000 claims abstract description 16
- 239000000975 dye Substances 0.000 claims abstract description 11
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- 239000002917 insecticide Substances 0.000 claims abstract description 5
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- -1 3-phenoxybenzyl Chemical group 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 239000000080 wetting agent Substances 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 238000001035 drying Methods 0.000 claims description 8
- 125000005843 halogen group Chemical group 0.000 claims description 8
- 239000002728 pyrethroid Substances 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 239000001273 butane Substances 0.000 claims description 7
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- 239000007787 solid Substances 0.000 claims description 6
- 229920003002 synthetic resin Polymers 0.000 claims description 6
- 239000000057 synthetic resin Substances 0.000 claims description 6
- 125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 claims description 5
- 239000000417 fungicide Substances 0.000 claims description 5
- 239000000654 additive Substances 0.000 claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 230000000855 fungicidal effect Effects 0.000 claims description 4
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 239000002184 metal Chemical class 0.000 claims description 4
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 3
- 230000000996 additive effect Effects 0.000 claims description 3
- MDIQXIJPQWLFSD-NJGYIYPDSA-N cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylic acid Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(O)=O MDIQXIJPQWLFSD-NJGYIYPDSA-N 0.000 claims description 3
- 230000035515 penetration Effects 0.000 claims description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 3
- 239000008158 vegetable oil Substances 0.000 claims description 3
- LLMLSUSAKZVFOA-UJURSFKZSA-N (1S,3R)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acid Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@@H]1C(O)=O LLMLSUSAKZVFOA-UJURSFKZSA-N 0.000 claims description 2
- 239000012963 UV stabilizer Substances 0.000 claims description 2
- QQODLKZGRKWIFG-UHFFFAOYSA-N cyfluthrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-UHFFFAOYSA-N 0.000 claims description 2
- 125000001033 ether group Chemical group 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims description 2
- XVSNMNYYRHUVGL-UHFFFAOYSA-N (4-methyl-1h-benzimidazol-2-yl) carbamate Chemical compound CC1=CC=CC2=C1NC(OC(N)=O)=N2 XVSNMNYYRHUVGL-UHFFFAOYSA-N 0.000 claims 1
- PTXMTZUUIOZOKF-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1,3-dioxolane Chemical compound ClC1=CC(Cl)=CC=C1C1OCCO1 PTXMTZUUIOZOKF-UHFFFAOYSA-N 0.000 claims 1
- 239000000470 constituent Substances 0.000 claims 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 claims 1
- 239000003755 preservative agent Substances 0.000 abstract description 2
- 239000003171 wood protecting agent Substances 0.000 description 14
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 11
- QQODLKZGRKWIFG-QSFXBCCZSA-N cyfluthrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-QSFXBCCZSA-N 0.000 description 11
- 229960001591 cyfluthrin Drugs 0.000 description 11
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 10
- 238000009835 boiling Methods 0.000 description 7
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 239000003921 oil Substances 0.000 description 6
- 235000019198 oils Nutrition 0.000 description 6
- 241000233866 Fungi Species 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 4
- FWSCAOIHIYZXES-UHFFFAOYSA-N 3-(2,2-dichloroethenyl)-1-[(4-fluoro-3-phenoxyphenyl)methyl]-2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)C(C=C(Cl)Cl)C1(C(O)=O)CC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 FWSCAOIHIYZXES-UHFFFAOYSA-N 0.000 description 3
- CCTFMNIEFHGTDU-UHFFFAOYSA-N 3-methoxypropyl acetate Chemical compound COCCCOC(C)=O CCTFMNIEFHGTDU-UHFFFAOYSA-N 0.000 description 3
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- 125000004093 cyano group Chemical group *C#N 0.000 description 3
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical group CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 3
- WURGXGVFSMYFCG-UHFFFAOYSA-N dichlofluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=CC=C1 WURGXGVFSMYFCG-UHFFFAOYSA-N 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
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- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
- VEQMUQZKBLIXLT-UHFFFAOYSA-N 2,3-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1C(C)C1C(O)=O VEQMUQZKBLIXLT-UHFFFAOYSA-N 0.000 description 2
- LDZYRENCLPUXAX-UHFFFAOYSA-N 2-methyl-1h-benzimidazole Chemical compound C1=CC=C2NC(C)=NC2=C1 LDZYRENCLPUXAX-UHFFFAOYSA-N 0.000 description 2
- 241000235349 Ascomycota Species 0.000 description 2
- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
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- 239000004480 active ingredient Substances 0.000 description 2
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- AKNQMEBLVAMSNZ-UHFFFAOYSA-N azaconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCCO1 AKNQMEBLVAMSNZ-UHFFFAOYSA-N 0.000 description 2
- 239000006013 carbendazim Substances 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 230000000749 insecticidal effect Effects 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- 230000003449 preventive effect Effects 0.000 description 2
- OJFZCPMENWLPRI-UHFFFAOYSA-N (2-ethylphenyl)-phenylmethanone Chemical compound CCC1=CC=CC=C1C(=O)C1=CC=CC=C1 OJFZCPMENWLPRI-UHFFFAOYSA-N 0.000 description 1
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 1
- JTPNRXUCIXHOKM-UHFFFAOYSA-N 1-chloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1 JTPNRXUCIXHOKM-UHFFFAOYSA-N 0.000 description 1
- BFNMOMYTTGHNGJ-UHFFFAOYSA-N 2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)CC1C(O)=O BFNMOMYTTGHNGJ-UHFFFAOYSA-N 0.000 description 1
- PZHXTCOVSRHUSS-UHFFFAOYSA-N 2-(2-phenylpropan-2-yloxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OC(C)(C)C1=CC=CC=C1 PZHXTCOVSRHUSS-UHFFFAOYSA-N 0.000 description 1
- IQHSSYROJYPFDV-UHFFFAOYSA-N 2-bromo-1,3-dichloro-5-(trifluoromethyl)benzene Chemical group FC(F)(F)C1=CC(Cl)=C(Br)C(Cl)=C1 IQHSSYROJYPFDV-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- ZMZNPVSNGBQGRW-UHFFFAOYSA-N 3-(2,2-dichloroethenyl)-2,2-dimethyl-1-[(3-phenoxyphenyl)methyl]cyclopropane-1-carboxylic acid Chemical compound CC1(C)C(C=C(Cl)Cl)C1(C(O)=O)CC1=CC=CC(OC=2C=CC=CC=2)=C1 ZMZNPVSNGBQGRW-UHFFFAOYSA-N 0.000 description 1
- JSEYDVLGSMLKDL-UHFFFAOYSA-N 4-[(4-ethoxyphenyl)diazenyl]naphthalen-1-ol Chemical compound C1=CC(OCC)=CC=C1N=NC1=CC=C(O)C2=CC=CC=C12 JSEYDVLGSMLKDL-UHFFFAOYSA-N 0.000 description 1
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- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 1
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- 241001523681 Dendrobium Species 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 241001399709 Dinoderus minutus Species 0.000 description 1
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- 241000415266 Ernobius mollis Species 0.000 description 1
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- 241001387516 Kalotermes flavicollis Species 0.000 description 1
- 241001174458 Kendrickiella phycomyces Species 0.000 description 1
- 235000001715 Lentinula edodes Nutrition 0.000 description 1
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- 241001465754 Metazoa Species 0.000 description 1
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- 241001147402 Monachus Species 0.000 description 1
- 241001504481 Monticola <Aves> Species 0.000 description 1
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- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000228143 Penicillium Species 0.000 description 1
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- 241001619461 Poria <basidiomycete fungus> Species 0.000 description 1
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- 241000590379 Reticulitermes santonensis Species 0.000 description 1
- 241001599571 Serpula <basidiomycete> Species 0.000 description 1
- 241001674251 Serpula lacrymans Species 0.000 description 1
- 241001177138 Sinoxylon Species 0.000 description 1
- 241001365173 Sirex juvencus Species 0.000 description 1
- 241000779819 Syncarpia glomulifera Species 0.000 description 1
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- 241001510583 Xyleborus Species 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 239000013011 aqueous formulation Substances 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 229950000294 azaconazole Drugs 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
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- 235000014113 dietary fatty acids Nutrition 0.000 description 1
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- 229940079593 drug Drugs 0.000 description 1
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- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
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- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
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- WIBFFTLQMKKBLZ-SEYXRHQNSA-N n-butyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCCC WIBFFTLQMKKBLZ-SEYXRHQNSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- MOQRZWSWPNIGMP-UHFFFAOYSA-N pentyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCC MOQRZWSWPNIGMP-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 239000001739 pinus spp. Substances 0.000 description 1
- 229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 1
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- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
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- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
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- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
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- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
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- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical class [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B27K3/343—Heterocyclic compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B27K3/38—Aromatic compounds
- B27K3/40—Aromatic compounds halogenated
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B27K3/50—Mixtures of different organic impregnating agents
Landscapes
- 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)
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3906556A DE3906556A1 (de) | 1989-03-02 | 1989-03-02 | Mittel oder konzentrat zum konservieren von holz oder holzwerkstoffen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD292172A5 true DD292172A5 (de) | 1991-07-25 |
Family
ID=6375287
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD90338232A DD292172A5 (de) | 1989-03-02 | 1990-02-28 | Mittel oder konzentrat zum konservieren von holz oder holzwerkstoffen |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US5248450A (es) |
| EP (2) | EP0385076B1 (es) |
| JP (1) | JPH02282307A (es) |
| AT (2) | ATE108718T1 (es) |
| DD (1) | DD292172A5 (es) |
| DE (3) | DE3906556A1 (es) |
| DK (2) | DK0577145T3 (es) |
| ES (1) | ES2058611T3 (es) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4142134A1 (de) * | 1991-12-20 | 1993-06-24 | Desowag Materialschutz Gmbh | Mittel oder konzentrat zum konservieren von holz und holzwerkstoffen |
| GB9202159D0 (en) * | 1992-01-31 | 1992-03-18 | Nc Dev Inc | Pesticidal treatment |
| DE4233337A1 (de) * | 1992-10-05 | 1994-04-07 | Bayer Ag | Mikrobizide Mittel |
| AU689480B2 (en) * | 1993-06-21 | 1998-04-02 | Bayer Aktiengesellschaft | Fungicidal active-substance combination |
| WO1995011786A1 (de) * | 1993-10-26 | 1995-05-04 | Bayer Aktiengesellschaft | Holzschutzmittel enthaltend eine kupferverbindung |
| JP3360383B2 (ja) * | 1993-12-20 | 2002-12-24 | 住友化学工業株式会社 | 殺虫組成物 |
| DE19513903A1 (de) * | 1995-04-12 | 1996-10-17 | Bayer Ag | Holzschutzmittel enthaltend eine Kupferverbindung |
| JP4017665B2 (ja) | 1995-09-29 | 2007-12-05 | ローム・アンド・ハース・カンパニー | 木材防腐剤 |
| DE19648888A1 (de) * | 1996-11-26 | 1998-05-28 | Remmers Bauchemie Gmbh | Wasserverdünnbares Konzentrat für den Holzschutz |
| US5906983A (en) * | 1997-08-20 | 1999-05-25 | The Clorox Company | High fructose containing insecticide compositions and methods of using the same |
| US6117854A (en) * | 1997-08-20 | 2000-09-12 | The Clorox Company | Enhanced performance insecticide compositions containing plant derived oil carriers and methods of using the same |
| US5856285A (en) * | 1997-10-31 | 1999-01-05 | Nouveau Technologies, Inc. | Polyurethane adhesive/sealant remover |
| DE19918730A1 (de) * | 1999-04-24 | 2000-10-26 | Bayer Ag | Wasserbasierte Formulierungen mit fungizider Wirkung |
| AUPR211400A0 (en) * | 2000-12-15 | 2001-01-25 | Koppers-Hickson Timber Protection Pty Limited | Material and method for treatment of timber |
| US8637089B2 (en) | 2003-04-09 | 2014-01-28 | Osmose, Inc. | Micronized wood preservative formulations |
| KR101110669B1 (ko) | 2003-04-09 | 2012-02-17 | 오스모스 인코포레이티드 | 미세화된 목재 방부제 제형 |
| GB2408511A (en) * | 2003-11-29 | 2005-06-01 | David George Cobbett | Preservative timber stain |
| US20070021385A1 (en) * | 2005-07-21 | 2007-01-25 | Jun Zhang | Compositions and methods for wood preservation |
| AU2006279671A1 (en) * | 2005-08-15 | 2007-02-22 | Osmose, Inc. | Water repellent composition for improving wood product dimensional stability |
| US20080175913A1 (en) * | 2007-01-09 | 2008-07-24 | Jun Zhang | Wood preservative compositions comprising isothiazolone-pyrethroids |
| DE102007043717A1 (de) | 2007-09-13 | 2009-03-19 | Remmers Baustofftechnik Gmbh | Holzschutzmittel |
| KR20120046242A (ko) * | 2009-07-08 | 2012-05-09 | 바이엘 크롭사이언스 아게 | 치환된 페닐(옥시/티오)알칸올 유도체 |
| CA2767385A1 (en) * | 2009-07-08 | 2011-01-13 | Bayer Cropscience Ag | Phenyl(oxy/thio)alkanol derivatives |
| GB201010439D0 (en) | 2010-06-21 | 2010-08-04 | Arch Timber Protection Ltd | A method |
| ES2387711B8 (es) * | 2011-03-03 | 2013-09-27 | Química De Munguía, S.A. (Quimunsa) | Producto para tratamiento de plantas. |
| GB201119139D0 (en) | 2011-11-04 | 2011-12-21 | Arch Timber Protection Ltd | Additives for use in wood preservation |
| JP2014101325A (ja) * | 2012-11-21 | 2014-06-05 | Japan Enviro Chemicals Ltd | 工業用防腐及び／又は防カビ剤 |
| JP2017514906A (ja) | 2014-05-02 | 2017-06-08 | アーチ ウッド プロテクション，インコーポレーテッド | 木材防腐剤組成物 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CY1259A (en) * | 1976-12-24 | 1984-11-23 | Wellcome Found | Synergistic parasiticidal compositions |
| DE2730515A1 (de) * | 1977-07-06 | 1979-01-18 | Bayer Ag | Substituierte phenoxybenzyloxycarbonylderivate, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide |
| NZ190600A (en) * | 1978-05-30 | 1982-03-09 | Wellcome Found | Arthropodicidal compositions containing cyclopropane-carboxylic acid ester derivatives |
| DE2833193A1 (de) * | 1978-07-28 | 1980-02-14 | Basf Ag | Insektizide mittel |
| AU542623B2 (en) * | 1980-05-16 | 1985-02-28 | Bayer Aktiengesellschaft | 1-hydroxyethyl-azole derivatives |
| DE3175673D1 (en) * | 1980-11-19 | 1987-01-15 | Ici Plc | Triazole compounds, a process for preparing them, their use as plant fungicides and fungicidal compositions containing them |
| FR2517176A1 (fr) * | 1981-12-01 | 1983-06-03 | Rhone Poulenc Agrochimie | Association insecticide et acaricide a base de pyrethroide |
| DE3202601A1 (de) * | 1982-01-27 | 1983-08-04 | Bayer Ag, 5090 Leverkusen | Substituierte 1 -hydroxyalkyl-azolyl-derivate, verfahren zu ihrer herstellung sowie ihrer verwendung als fungizide und pflanzenwachstumsregulatoren |
| DE3333412A1 (de) * | 1983-09-16 | 1985-04-04 | Bayer Ag, 5090 Leverkusen | Fungizide mittel |
| DE3333411A1 (de) * | 1983-09-16 | 1985-04-04 | Bayer Ag, 5090 Leverkusen | Fungizide mittel |
| ATE44354T1 (de) * | 1985-04-13 | 1989-07-15 | Desowag Materialschutz Gmbh | Holzkonservierungsmittel. |
| DE3621494A1 (de) * | 1986-06-27 | 1988-01-07 | Bayer Ag | Verwendung von 1-aryl-3-hydroxy-3-alkyl-4-(1,2,4-triazol-1-yl) -butan-derivaten als mikrobizide fuer den materialschutz |
| DE3641555A1 (de) * | 1986-12-05 | 1988-06-16 | Solvay Werke Gmbh | Mittel oder konzentrat zum konservieren von holz und holzwerkstoffen |
-
1989
- 1989-03-02 DE DE3906556A patent/DE3906556A1/de not_active Withdrawn
-
1990
- 1990-01-16 ES ES90100818T patent/ES2058611T3/es not_active Expired - Lifetime
- 1990-01-16 DK DK93110978.9T patent/DK0577145T3/da active
- 1990-01-16 AT AT90100818T patent/ATE108718T1/de not_active IP Right Cessation
- 1990-01-16 EP EP90100818A patent/EP0385076B1/de not_active Expired - Lifetime
- 1990-01-16 EP EP93110978A patent/EP0577145B1/de not_active Expired - Lifetime
- 1990-01-16 DE DE59010685T patent/DE59010685D1/de not_active Expired - Fee Related
- 1990-01-16 AT AT93110978T patent/ATE150354T1/de not_active IP Right Cessation
- 1990-01-16 DK DK90100818.5T patent/DK0385076T3/da active
- 1990-01-16 DE DE59006463T patent/DE59006463D1/de not_active Expired - Fee Related
- 1990-02-28 DD DD90338232A patent/DD292172A5/de not_active IP Right Cessation
- 1990-02-28 US US07/485,890 patent/US5248450A/en not_active Expired - Fee Related
- 1990-03-02 JP JP2049667A patent/JPH02282307A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| ES2058611T3 (es) | 1994-11-01 |
| ATE108718T1 (de) | 1994-08-15 |
| DE59006463D1 (de) | 1994-08-25 |
| EP0385076B1 (de) | 1994-07-20 |
| US5248450A (en) | 1993-09-28 |
| DK0385076T3 (da) | 1994-08-22 |
| ATE150354T1 (de) | 1997-04-15 |
| EP0577145A1 (de) | 1994-01-05 |
| DE59010685D1 (de) | 1997-04-24 |
| DK0577145T3 (da) | 1997-09-22 |
| EP0577145B1 (de) | 1997-03-19 |
| EP0385076A1 (de) | 1990-09-05 |
| DE3906556A1 (de) | 1990-09-06 |
| JPH02282307A (ja) | 1990-11-19 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| NAC | Public notice for inspection of provisional exclusive patent accord. to par 18/2 dd-patg. | ||
| RPI | Change in the person, name or address of the patentee (searches according to art. 11 and 12 extension act) | ||
| RPV | Change in the person, the name or the address of the representative (searches according to art. 11 and 12 extension act) | ||
| ENJ | Ceased due to non-payment of renewal fee |