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NO167013B - PROCEDURE FOR FIGHTING SUSPENS WHICH DAMAGE TO WOODS - Google Patents

PROCEDURE FOR FIGHTING SUSPENS WHICH DAMAGE TO WOODS Download PDF

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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
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NO
Norway
Prior art keywords
wood
fungi
damage
dimethyl
tridecyl
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Application number
NO860755A
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Norwegian (no)
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NO860755L (en
NO167013C (en
Inventor
Wolfgang Reuther
Horst Sommer
Dietrich Mangold
Ernst-Heinrich Pommer
Hans-Volker Borck
Original Assignee
Basf Ag
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Publication of NO860755L publication Critical patent/NO860755L/en
Publication of NO167013B publication Critical patent/NO167013B/en
Publication of NO167013C publication Critical patent/NO167013C/en

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, 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
    • A01N43/84Biocides, 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27KPROCESSES, 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
    • B27K3/00Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
    • B27K3/34Organic impregnating agents
    • B27K3/343Heterocyclic compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27KPROCESSES, 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
    • B27K3/00Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
    • B27K3/34Organic impregnating agents
    • B27K3/36Aliphatic compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27KPROCESSES, 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
    • B27K3/00Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
    • B27K3/34Organic impregnating agents
    • B27K3/50Mixtures of different organic impregnating agents

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  • 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

1. A method of controlling fungi which damage wood, wherein the fungi, or the wood threatened by fungal infestation, excluding wood from rubber trees, is treated with N-tridecyl-2,6-dimethylmorpholine, except in the form of an aqueous solution which contains a 1,3-butadiene polymer as a solubilizer.

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)

Fremgangsmåte ved bekjempelse av sopp som skader treverk, karakterisert ved at man behandler soppene eller trevirket som er truet av soppangrep, unntatt trevirke fra gummitrær, med N-tridecyl-2,6-dimetylmorfolin.Method for combating fungi that damage wood, characterized by treating the fungi or the wood that is threatened by fungal attack, except wood from rubber trees, with N-tridecyl-2,6-dimethylmorpholine.
NO860755A 1985-03-02 1986-02-28 PROCEDURE FOR FIGHTING SUSPENS WHICH DAMAGE TO WOODS NO167013C (en)

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

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ID=6264020

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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)

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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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

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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