NO167013B - PROCEDURE FOR FIGHTING SUSPENS WHICH DAMAGE TO WOODS - Google Patents
PROCEDURE FOR FIGHTING SUSPENS WHICH DAMAGE TO WOODS Download PDFInfo
- Publication number
- NO167013B NO167013B NO860755A NO860755A NO167013B NO 167013 B NO167013 B NO 167013B NO 860755 A NO860755 A NO 860755A NO 860755 A NO860755 A NO 860755A NO 167013 B NO167013 B NO 167013B
- Authority
- NO
- Norway
- Prior art keywords
- wood
- fungi
- damage
- dimethyl
- tridecyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 4
- 239000002023 wood Substances 0.000 claims abstract description 23
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 claims abstract description 14
- 241000233866 Fungi Species 0.000 claims abstract description 13
- 230000002538 fungal effect Effects 0.000 claims abstract description 11
- 244000043261 Hevea brasiliensis Species 0.000 claims abstract description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 2
- 206010061217 Infestation Diseases 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000013543 active substance Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 229920001817 Agar Polymers 0.000 description 5
- 239000008272 agar Substances 0.000 description 5
- 239000004480 active ingredient Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000010409 ironing Methods 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- YTOPFCCWCSOHFV-RTBURBONSA-N (2r,6r)-2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1C[C@@H](C)O[C@H](C)C1 YTOPFCCWCSOHFV-RTBURBONSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- XGWIJUOSCAQSSV-XHDPSFHLSA-N (S,S)-hexythiazox Chemical compound S([C@H]([C@@H]1C)C=2C=CC(Cl)=CC=2)C(=O)N1C(=O)NC1CCCCC1 XGWIJUOSCAQSSV-XHDPSFHLSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241000094558 Antrodia sinuosa Species 0.000 description 2
- 241000221198 Basidiomycota Species 0.000 description 2
- 241001600095 Coniophora puteana Species 0.000 description 2
- 241001492300 Gloeophyllum trabeum Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 241000222355 Trametes versicolor Species 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000003171 wood protecting agent Substances 0.000 description 2
- KEUPLGRNURQXAR-UHFFFAOYSA-N (4-chlorophenyl) acetate Chemical compound CC(=O)OC1=CC=C(Cl)C=C1 KEUPLGRNURQXAR-UHFFFAOYSA-N 0.000 description 1
- PLMBMEXGGQWUDS-UHFFFAOYSA-N 1-[2-[2-(2,4-dichlorophenyl)-1,3-dioxolan-2-yl]ethyl]-1,2,4-triazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CCN2N=CN=C2)OCCO1 PLMBMEXGGQWUDS-UHFFFAOYSA-N 0.000 description 1
- DPGXTUOZQHBZRC-UHFFFAOYSA-N 1-[2-[2-(2,4-dichlorophenyl)-4-ethyl-1,3-dioxolan-2-yl]ethyl]-1,2,4-triazole Chemical compound O1C(CC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CCN1N=CN=C1 DPGXTUOZQHBZRC-UHFFFAOYSA-N 0.000 description 1
- FBGKAFRWBNEYTR-UHFFFAOYSA-N 1-[2-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-yl]ethyl]-1,2,4-triazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CCN1N=CN=C1 FBGKAFRWBNEYTR-UHFFFAOYSA-N 0.000 description 1
- RULKYXXCCZZKDZ-UHFFFAOYSA-N 2,3,4,5-tetrachlorophenol Chemical compound OC1=CC(Cl)=C(Cl)C(Cl)=C1Cl RULKYXXCCZZKDZ-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- 241000235349 Ascomycota Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241001600093 Coniophora Species 0.000 description 1
- 241000221785 Erysiphales Species 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- QTDRLOKFLJJHTG-UHFFFAOYSA-N Furmecyclox Chemical compound C1=C(C)OC(C)=C1C(=O)N(OC)C1CCCCC1 QTDRLOKFLJJHTG-UHFFFAOYSA-N 0.000 description 1
- 244000162269 Lentinus lepideus Species 0.000 description 1
- 235000017066 Lentinus lepideus Nutrition 0.000 description 1
- 241000318230 Merulius Species 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241001581437 Polystictus Species 0.000 description 1
- 241000221535 Pucciniales Species 0.000 description 1
- 244000082988 Secale cereale Species 0.000 description 1
- 241001674251 Serpula lacrymans Species 0.000 description 1
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000011230 binding agent 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
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 1
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 1
- 239000011093 chipboard Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229940120693 copper naphthenate Drugs 0.000 description 1
- SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- QQQYTWIFVNKMRW-UHFFFAOYSA-N diflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(Cl)C=C1 QQQYTWIFVNKMRW-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000001034 iron oxide pigment Substances 0.000 description 1
- 229960002809 lindane Drugs 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- DECZQJJTUZWGMA-UHFFFAOYSA-N methyl-(2-propoxyphenyl)carbamic acid Chemical compound CCCOC1=CC=CC=C1N(C)C(O)=O DECZQJJTUZWGMA-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 150000002780 morpholines Chemical class 0.000 description 1
- AKBZLSDTRZFLRP-UHFFFAOYSA-N n-cyclohexylnitrous amide Chemical class O=NNC1CCCCC1 AKBZLSDTRZFLRP-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000006916 nutrient agar Substances 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- JUEAPPHORMOWPK-UHFFFAOYSA-M tributylstannyl benzoate Chemical compound CCCC[Sn](CCCC)(CCCC)OC(=O)C1=CC=CC=C1 JUEAPPHORMOWPK-UHFFFAOYSA-M 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [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
- 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
- A01N43/84—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 six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
-
- 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
- B27K3/36—Aliphatic 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
- B27K3/50—Mixtures of different organic impregnating agents
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
- Photometry And Measurement Of Optical Pulse Characteristics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyrrole Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
Description
Foreliggende oppfinnelse vedrører en fremgangsmåte ved bekjempelse av sopp som skader treverk. The present invention relates to a method for combating fungi that damage wood.
Det erkjent fra tysk off.skrift 1.164.152 å anvende substituerte morfolinderivater i jordbruket for bekjempelse av fytopatogene sopper. Et tyngdepunkt ved anvendelsen av disse virkestoffer, spesielt av N-tridecyl-2,6-dimetylmorfolin (tridemorf) ligger derunder i korn i bekjempelse av ekte meldugg-sopper som tilhører soppklassen Ascomyceter. Kornrust-sopper såsom rugdvergrust og hvetebrunrust som tilhører soppklassen Basidiomyceter bekjempes ikke med tridemorf. It is recognized from German official publication 1,164,152 to use substituted morpholine derivatives in agriculture to combat phytopathogenic fungi. A center of gravity in the use of these active substances, especially of N-tridecyl-2,6-dimethylmorpholine (tridemorph) lies underneath in grain in combating true powdery mildew fungi belonging to the fungal class Ascomycetes. Grain rust fungi such as rye dwarf rust and wheat brown rust which belong to the Basidiomycetes class of fungi are not controlled with tridemorph.
Det er videre kjent å anvende N-tridecyl-2,6-trans-dimetyl-morfolin for bekjempelse av sopper som ødelegger trevirke såsom Coniophora og Polystictus (EP 129.211). It is also known to use N-tridecyl-2,6-trans-dimethyl-morpholine for combating wood-destroying fungi such as Coniophora and Polystictus (EP 129,211).
Det er nå overraskende funnet at N-tridecyl-2,6-dimetyl-morf olin i sammenligning med N-tridecyl-2,6-trans-dimetyl-morfolin viser en vesentlig bedre virksomhet mot slike sopper, som angriper og ødelegger trevirke, spesielt ikke lenger levende trevirke. It has now surprisingly been found that N-tridecyl-2,6-dimethyl-morpholine in comparison with N-tridecyl-2,6-trans-dimethyl-morpholine shows a significantly better activity against such fungi, which attack and destroy wood, especially no longer living wood.
Foreliggende oppfinnelse ligger derfor i at man behandler soppene eller trevirket som er truet av soppangrep, unntatt trevirke fra gummitrær, med N-tridecyl-2,6-dimetylmorfolin. The present invention therefore consists in treating the fungi or wood that is threatened by fungal attack, except for wood from rubber trees, with N-tridecyl-2,6-dimethylmorpholine.
Følgende sopper som ødeleggeer trevirke (Basidiomyceter) lar seg ifølge oppfinnelsen f.eks. bekjempe med trevirke-beskyttelsesmiddelet: Merulius lacrimans, Coniophora puteana, Lentinus lepideus, Lenzites trabea, Polystictus versicolor, Poria vaporaria. According to the invention, the following wood-destroying fungi (Basidiomycetes) can be used, e.g. fight with the wood preservative: Merulius lacrimans, Coniophora puteana, Lentinus lepideus, Lenzites trabea, Polystictus versicolor, Poria vaporaria.
Ikke lenger levende (dødt) trevirke er f.eks. skåret trevirke, bygningstrevirke, trevirkestoffer, f.eks. sponplater, trespon. Med N-tridecyl-2,6-dimetylmorfolin menes både virkestoffet selv og dets salter med uorganiske eller organiske syrer, f.eks. salter med hydrogenfluorid, saltsyre, hydrogen-bromid, svovelsyre, eddiksyre og propionsyre. No longer living (dead) wood is e.g. cut wood, construction wood, wood materials, e.g. chipboard, wood shavings. By N-tridecyl-2,6-dimethylmorpholine is meant both the active substance itself and its salts with inorganic or organic acids, e.g. salts with hydrogen fluoride, hydrochloric acid, hydrogen bromide, sulfuric acid, acetic acid and propionic acid.
Virkestoffet kan anvendes i preparater eåsom løsninger, emulsjoner, pastaer, strykemidler (f.eks. maling, beis) og oljedispersjoner. Preparatene inneholder generelt mellom 0,1 The active substance can be used in preparations such as solutions, emulsions, pastes, ironing agents (eg paint, stain) and oil dispersions. The preparations generally contain between 0.1
og 90 vekt% virkestoff, fortrinnsvis 0,25 til 50%. Bruksmengden er avhengig av den virkning man ønsker å oppnå 0,5 til 8 g and 90% by weight active substance, preferably 0.25 to 50%. The amount used depends on the effect you want to achieve, 0.5 to 8 g
virkestoff pr. m<2> trevirkeoverflate som skal beskyttes henholds-vis 50 til 4000 g virkestoff pr. m<3> trevirke. Strykemidler inneholder f.eks. 0,5 til 4 vekt% virkestoff. For beskyttelse av trevirkestoffer kan virkestoffene tilsettes bindemidlet i form av emulsjon, f.eks. i mengder på 2 til 6 vekt%. active ingredient per m<2> wooden surface to be protected respectively 50 to 4000 g of active substance per m<3> wood. Ironing agents contain e.g. 0.5 to 4% by weight of active ingredient. To protect wood substances, the active substances can be added to the binder in the form of an emulsion, e.g. in amounts of 2 to 6% by weight.
Applikasjon av virkestoffet finner sted på vanlig måte, f.eks. ved strykning, sprøyting, spruting, dypping eller trykk-impregnerings- eller diffusjonsmetoder. Application of the active substance takes place in the usual way, e.g. by ironing, spraying, spraying, dipping or pressure impregnation or diffusion methods.
De følgende eksempler skal anskueliggjøre oppfinnelsen (prosenter i vekt%). The following examples shall illustrate the invention (percentages by weight%).
Eksempel 1 Example 1
Trevirkebeskyttelsesgrunning farveløs Wood protection primer colorless
2,00% tridemorf 2.00% tridemorph
0,10% permetri.n 0.10% permetri.n
0,50% diklofluanid 0.50% diclofluanid
6,00% linolje 6.00% linseed oil
91,40% prøvebensin (kp. 180-220°C) 91.40% test gasoline (bp. 180-220°C)
Eksempel 2 Example 2
Trevi rkebeskyttelsesglasur, farvet Trevi frost protection glaze, colored
1,00% tridemorf 1.00% tridemorph
0,10% permetri.n 0.10% permetri.n
0,50% diklofluanid 0.50% diclofluanid
15,00% alkydharpiks 15.00% alkyd resin
3,00% butylglykol 3.00% butyl glycol
3,00% jernoksydpigment 3.00% iron oxide pigment
0,20% tørkemiddel 0.20% desiccant
77,20% prøvebensin (kp. 180-220°C) 77.20% test gasoline (bp. 180-220°C)
Eksempel 3 Example 3
Vakuumimpregneringsolje Vacuum impregnation oil
2,00% tridemorf 2.00% tridemorph
0,50% diklofluanid 0.50% diclofluanid
3,00% di.butylftalat 3.00% dibutyl phthalate
94,50% prøvebensin (kp. 180-220°C) 94.50% test petrol (bp. 180-220°C)
Eksempel 4 Example 4
Trevi rkebeskyttelsesgrunni ng, vannfortynnbar 2,00% tridemorf Trevi rain protection primer, water-dilutable 2.00% tridemorph
3,00% dimetylalkylberizylammoni umklori d 3.00% dimethylalkylberizylammonium umchlori d
1,00% addisjonsprodukt av etylenoksyd (EO) til 1.00% addition product of ethylene oxide (EO) to
nonylfenol (ca. 10 mol EO pr. mol fenol) nonylphenol (approx. 10 mol EO per mol phenol)
3,00% eddiksyre 3.00% acetic acid
5,00% propylenglykol 5.00% propylene glycol
86,00% vann 86.00% water
For å utvide virkningsspektret eller for å oppnå spesielle virkninger kan virkestoffene kombineres med andre virkestoffer. Som spesielt heldig anses blandinger med følgende forbindelser: Organotinnforbindelser såsom tributyltinnoksyd og tributyl-ti nnbenzoat To extend the spectrum of action or to achieve special effects, the active substances can be combined with other active substances. Mixtures with the following compounds are considered particularly fortunate: Organotin compounds such as tributyl tin oxide and tributyl tin benzoate
metylenbi sti ocyanat methylene bi sti ocyanate
dimetylalkylaminsalter dimethylalkylamine salts
dimetyldi alkylammoni um-klori der dimethyldialkylammonium chloride there
dimetylalkylbenzylammonium-klorider dimethylalkylbenzylammonium chlorides
trimetylalkylammoni um-klorider trimethylalkylammonium chlorides
dimetylbi pyridi ni um-klori d dimethyl bi pyridi ni um-chlori d
cetylpyri di ni um-klori d cetylpyri di ni um-chlori d
klorerte fenoler, såsom tetra- og pentaklorfenol tetraklori softalsyre-di ni tri 1 chlorinated phenols, such as tetra- and pentachlorophenol tetrachlorosofthalic acid dinitri 1
2-halogenbenzosyreanilid 2-Halobenzoic acid anilide
N-cykloheksyl-N-metoksy-2,5-dimetyl-furan-3-karboksylsyreamid N,N-dimetyl-N'-fenyl-(N-fluormetylti o)-sulfami d N,N-dimety1-N1-tolyl-(N-fluormetylti o)-sulfami d benzimi dazol-2-karbaminsyre-metylester N-cyclohexyl-N-methoxy-2,5-dimethyl-furan-3-carboxylic acid amide N,N-dimethyl-N'-phenyl-(N-fluoromethylthio)-sulfamid N,N-dimethyl-N1-tolyl-( N-fluoromethylthio)-sulfami d benzimidazole-2-carbamic acid methyl ester
2-ti ocyanomety1-ti obenzoti azol 2-thi ocyanomethy1-thi obenzothi azole
kobbernaftenat copper naphthenate
kobber-8-oksyki noli n copper-8-oxyki noli n
alkali- og metallsalter av N'-hydroksy-N-cykloheksyl-di azeni umoksyder ^alkali and metal salts of N'-hydroxy-N-cyclohexyl-diazenium oxides ^
1-(1',2',4'-tri azolyl-1')-[1-(4'-klorfenoksy)]-3,3-dimetyl-butan-2-on 1-(1',2',4'-triazolyl-1')-[1-(4'-chlorophenoxy)]-3,3-dimethyl-butan-2-one
1-(1<1>,2'-4'-triazolyl-1')-[1-(4'-klorfenoksy)]-3,3-dimetyl-butan-2-ol 1-(1<1>,2'-4'-triazolyl-1')-[1-(4'-chlorophenoxy)]-3,3-dimethyl-butan-2-ol
N-[3,(p-tert.-butylfenyl)-2-mety1-propyl]-cis-2,6-dimetylmorfoli n heksaklorcykloheksan N-[3,(p-tert-butylphenyl)-2-methyl-propyl]-cis-2,6-dimethylmorpholine hexachlorocyclohexane
0,0-di etyl-o-(a-cyanbenzyli den-ami no-ti ofosfat 0,0-diethyl-o-(a-cyanobenzylidene-amino-thiophosphate).
0,0-di.etyl-o-3. 5.6. - tri klor-2-pyri di 1-ti ono-f os f at 0,0-diety1-ditio-fosforyl-metyl-6-klorbenzoksazolon 2- i-propoksyfenyl-N-metyl-karbamat 0,0-di.ethyl-o-3. 5.6. - trichloro-2-pyridi 1-thiono-phos ph at 0,0-diethy1-dithio-phosphoryl-methyl-6-chlorobenzoxazolone 2-i-propoxyphenyl-N-methyl-carbamate
N-metyl-l-naftyl-karbamat N-methyl-1-naphthyl-carbamate
norbornen-di.metanolheksa-klorcyklosulf i tt norbornene-di.methanolhexa-chlorocyclosulf in tt
1-(4-klorfenyl)-3-(2.6-di-fluorbenzoyl)-urea 1-(4-Chlorophenyl)-3-(2,6-difluorobenzoyl)-urea
1-[2-(2,4-di klorfenyl)-1,3-dioksolan-2-yl-etyl]-1H-1,2,4-tri azol 1-[2-(2,4-dichlorophenyl)-1,3-dioxolan-2-yl-ethyl]-1H-1,2,4-triazole
1-[2-(2,4-diklorfenyl)-4-etyl-l,3-dioksolan-2-yl-etyl]-1H-1,2,4-tri azol 1-[2-(2,4-Dichlorophenyl)-4-ethyl-1,3-dioxolan-2-yl-ethyl]-1H-1,2,4-triazole
1- [ 2- (2 ,4-diklorf enyl) -4-n-propyl-l, 3-di.oksolan-2-yl-etyl] - 1H-1,2,4-triazol 1-[2-(2,4-dichlorophenyl)-4-n-propyl-1,3-dioxolan-2-yl-ethyl]-1H-1,2,4-triazole
Syntetiske pyretroider såsom Synthetic pyrethroids such as
(±) -3- (2. 2-diklorvi.nyl-2 . 2-dimetyl) -cyklopropan-l-karboksylsyre-3- fenoksy-benzylester (±)-3-(2.2-dichlorovinyl-2.2-dimethyl)-cyclopropane-1-carboxylic acid 3-phenoxy-benzyl ester
3- (2 . 2-diklorvi.ny 1-2. 2-dimety1) -cyklopropan-l-karboksylsyre-ct-cyano-3-f enoksybenzylester 3-(2.2-dichloroviny1-2.2-dimethyl)-cyclopropane-1-carboxylic acid ct-cyano-3-phenoxybenzyl ester
3- (2 . 2-dibromvinyl-2 . 2-di.metyl) -a-cyano-m-f enoksybenzyl (IR, 3R) - cyklopropan-karboksylat 3-(2.2-dibromovinyl-2.2-dimethyl)-α-cyano-m-phenoxybenzyl (IR, 3R)-cyclopropane carboxylate
a-cyano-3-f enoksybenzyl-i.sopropyl-2 . 4-klorf enylacetat Eksempel 5 α-cyano-3-phenoxybenzyl-isopropyl-2. 4-Chlorophenyl acetate Example 5
For å fremstille et oljeaktig trevirke-beskyttelsesmiddel med 1% virkestoff oppløses først 1 del (vektdel) av virkestoffet under svak oppvarming i 55 deler av en aromatrik bensinfraksjon. Så tilsettes 10 deler av en alkydharpiks og kompletteres med prøvebensin ved romtemperatur til 100 deler. To prepare an oily wood preservative with 1% active ingredient, first dissolve 1 part (part by weight) of the active ingredient under gentle heating in 55 parts of an aromatic gasoline fraction. Then 10 parts of an alkyd resin are added and supplemented with test gasoline at room temperature to 100 parts.
For å fremstille vannavstøtende impregneringsmidler kan To produce water-repellent impregnating agents can
de oljeaktige trevirke-beskyttelsesmidler tilsettes såkalte "water repellents". Egnede substanser er f.eks. sinkstearat, alumi.niumstearat og vokser. so-called "water repellents" are added to the oily wood preservatives. Suitable substances are e.g. zinc stearate, aluminum stearate and waxes.
Videre kan det for å oppnås farveeffekte* innarbeides finpartiklede uorganiske eller organiske pigmenter eller olje-løselige farvestoffer i formuleringene. Furthermore, in order to achieve a color effect*, fine-particle inorganic or organic pigments or oil-soluble dyes can be incorporated into the formulations.
For å beskytte trevirke mot soppangrep påføres normalt To protect wood against fungal attack is normally applied
50 til 200 ml av de i eks. 5 oppførte oljeaktige trevirke-beskyttelsesmidler pr. m 2 trevirkeoverflate ved strykning, sprøyting eller dypping. 50 to 200 ml of those in ex. 5 listed oily wood preservatives per m 2 wooden surface by ironing, spraying or dipping.
Anve ndelseseksempel 1 Application example 1
Tridemorf oppløses i aceton i mengder fra 100, trinnvis til 3 ppm og tilsettes en 5%ig maltekstraktagar. Agaren helles 1 petri-skåler og etter stivning inokkuleres de fungicid-holdige næringsagarplater adskilt med myzele av trevirke-angripende sopper Merculius lacrimans (ekte hussopp), Coniophora puteana (kjellersopp), Lenzites trabea, Polystictus versicolor og Poria vaporaria. Etter 5 dagers utvikling av skålene ved 2 5°C vurderes utviklingen av sopp-kolonier på næringsbunnen sammenlignet med N-tridecyl-2,6-trans-dimetylmorfolin (A) Tridemorph is dissolved in acetone in quantities from 100, step by step to 3 ppm and a 5% malt extract agar is added. The agar is poured into 1 petri dish and, after solidification, the fungicide-containing nutrient agar plates are inoculated separately with the mycelium of the wood-attacking fungi Merculius lacrimans (true house fungus), Coniophora puteana (cellar fungus), Lenzites trabea, Polystictus versicolor and Poria vaporaria. After 5 days of development of the dishes at 25°C, the development of fungal colonies on the nutrient medium is assessed compared to N-tridecyl-2,6-trans-dimethylmorpholine (A)
og kontrollen (uten fungicid-tilsetning). and the control (without fungicide addition).
0 = ingen soppvekst (soppmyzel drept) 0 = no fungal growth (fungal mycelium killed)
1 = litt soppvekst (opptil 1/3 av agaroverflaten bevokst) 1 = some fungal growth (up to 1/3 of the agar surface covered)
2 = middels soppvekst (opptil 2/3 av agaroverflaten bevokst) 2 = medium fungal growth (up to 2/3 of the agar surface covered)
5 = uhemmet soppvekst (hele agaroverflaten bevokst) 5 = unrestrained fungal growth (entire agar surface overgrown)
Anvendelseseksempel 2 Application example 2
Følgende grenseverdier, d.v.s. den nødvendige mengde av virkestoffet tridemorf for beskyttelse av 1 m 3 trevirke ble The following limit values, i.e. the required amount of the active substance tridemorph for the protection of 1 m 3 of wood was
målt etter forutgående utvasking med vann. measured after previous washing out with water.
4r 4 years
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19853507420 DE3507420A1 (en) | 1985-03-02 | 1985-03-02 | WOOD PRESERVATIVES |
Publications (3)
Publication Number | Publication Date |
---|---|
NO860755L NO860755L (en) | 1986-09-03 |
NO167013B true NO167013B (en) | 1991-06-17 |
NO167013C NO167013C (en) | 1991-09-25 |
Family
ID=6264020
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO860755A NO167013C (en) | 1985-03-02 | 1986-02-28 | PROCEDURE FOR FIGHTING SUSPENS WHICH DAMAGE TO WOODS |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0193890B1 (en) |
JP (1) | JPH07115327B2 (en) |
AT (1) | ATE37157T1 (en) |
CA (1) | CA1272853A (en) |
DE (2) | DE3507420A1 (en) |
FI (1) | FI860750L (en) |
NO (1) | NO167013C (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3539412A1 (en) * | 1985-11-07 | 1987-05-14 | Basf Ag | WOOD PRESERVATIVES |
DE3641554C2 (en) * | 1986-12-05 | 1995-04-06 | Solvay Werke Gmbh | Wood preservatives |
DE3736298A1 (en) * | 1987-10-27 | 1989-05-11 | Wolman Gmbh Dr | WOOD PRESERVATIVES |
DE3839640A1 (en) * | 1988-11-24 | 1990-05-31 | Wolman Gmbh Dr | WOOD PRESERVATIVES |
CH681436A5 (en) * | 1990-04-26 | 1993-03-31 | Warmoctro Bv | |
CH681440A5 (en) * | 1990-04-26 | 1993-03-31 | Warmoctro Bv | |
CH681437A5 (en) * | 1990-04-26 | 1993-03-31 | Warmoctro Bv | |
CH681438A5 (en) * | 1990-04-26 | 1993-03-31 | Warmoctro Bv |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3121349A1 (en) * | 1981-05-29 | 1982-12-16 | Basf Ag, 6700 Ludwigshafen | CYCLOHEXEN DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND FUNGICIDES CONTAINING THEM |
DE3321712A1 (en) * | 1983-06-16 | 1984-12-20 | Basf Ag, 6700 Ludwigshafen | 2,6-TRANS-DIMETHYLMORPHOLINE DERIVATIVES AND FUNGICIDES CONTAINING THEM AND METHOD FOR CONTROLLING FUNGI |
DE3329694A1 (en) * | 1983-08-17 | 1985-03-07 | Dr. Wolman Gmbh, 7573 Sinzheim | AQUEOUS WOOD PRESERVATIVE |
-
1985
- 1985-03-02 DE DE19853507420 patent/DE3507420A1/en not_active Withdrawn
-
1986
- 1986-02-20 FI FI860750A patent/FI860750L/en not_active Application Discontinuation
- 1986-02-26 JP JP61039351A patent/JPH07115327B2/en not_active Expired - Lifetime
- 1986-02-27 CA CA000502836A patent/CA1272853A/en not_active Expired - Lifetime
- 1986-02-28 EP EP86102615A patent/EP0193890B1/en not_active Expired
- 1986-02-28 DE DE8686102615T patent/DE3660709D1/en not_active Expired
- 1986-02-28 NO NO860755A patent/NO167013C/en unknown
- 1986-02-28 AT AT86102615T patent/ATE37157T1/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
ATE37157T1 (en) | 1988-09-15 |
NO860755L (en) | 1986-09-03 |
NO167013C (en) | 1991-09-25 |
DE3660709D1 (en) | 1988-10-20 |
JPH07115327B2 (en) | 1995-12-13 |
JPS61202801A (en) | 1986-09-08 |
FI860750A0 (en) | 1986-02-20 |
EP0193890B1 (en) | 1988-09-14 |
CA1272853A (en) | 1990-08-21 |
EP0193890A1 (en) | 1986-09-10 |
FI860750L (en) | 1986-09-03 |
DE3507420A1 (en) | 1986-09-04 |
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