NO176088B - Wood preservative and its use - Google Patents
Wood preservative and its use Download PDFInfo
- Publication number
- NO176088B NO176088B NO884758A NO884758A NO176088B NO 176088 B NO176088 B NO 176088B NO 884758 A NO884758 A NO 884758A NO 884758 A NO884758 A NO 884758A NO 176088 B NO176088 B NO 176088B
- Authority
- NO
- Norway
- Prior art keywords
- acid
- water
- wood
- wood preservative
- benzimidazole
- Prior art date
Links
- 239000003171 wood protecting agent Substances 0.000 title claims abstract description 10
- 239000002253 acid Substances 0.000 claims abstract description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000002023 wood Substances 0.000 claims description 30
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 15
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 claims description 14
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 6
- -1 dimethyl alkylamine Chemical class 0.000 claims description 6
- OEOIWYCWCDBOPA-UHFFFAOYSA-N 6-methyl-heptanoic acid Chemical compound CC(C)CCCCC(O)=O OEOIWYCWCDBOPA-UHFFFAOYSA-N 0.000 claims description 4
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 claims description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 3
- 229920000847 nonoxynol Polymers 0.000 claims description 3
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 claims description 3
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 claims description 2
- RILZRCJGXSFXNE-UHFFFAOYSA-N 2-[4-(trifluoromethoxy)phenyl]ethanol Chemical compound OCCC1=CC=C(OC(F)(F)F)C=C1 RILZRCJGXSFXNE-UHFFFAOYSA-N 0.000 claims description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 abstract 1
- LKUBWDNDGBVKFK-UHFFFAOYSA-N methyl 1h-benzimidazole-2-carboxylate Chemical compound C1=CC=C2NC(C(=O)OC)=NC2=C1 LKUBWDNDGBVKFK-UHFFFAOYSA-N 0.000 abstract 1
- 239000003755 preservative agent Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 7
- 241000233866 Fungi Species 0.000 description 5
- 239000012141 concentrate Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000005470 impregnation Methods 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 230000000855 fungicidal effect Effects 0.000 description 3
- 239000000417 fungicide Substances 0.000 description 3
- 244000025254 Cannabis sativa Species 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 2
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 2
- 239000002798 polar solvent Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- RYAUSSKQMZRMAI-YESZJQIVSA-N (S)-fenpropimorph Chemical compound C([C@@H](C)CC=1C=CC(=CC=1)C(C)(C)C)N1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-YESZJQIVSA-N 0.000 description 1
- TUBQDCKAWGHZPF-UHFFFAOYSA-N 1,3-benzothiazol-2-ylsulfanylmethyl thiocyanate Chemical compound C1=CC=C2SC(SCSC#N)=NC2=C1 TUBQDCKAWGHZPF-UHFFFAOYSA-N 0.000 description 1
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 description 1
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 1
- LWPLSMSFAZPBGO-UHFFFAOYSA-N 1-dodecyl-2h-pyridine;hydrochloride Chemical compound Cl.CCCCCCCCCCCCN1CC=CC=C1 LWPLSMSFAZPBGO-UHFFFAOYSA-N 0.000 description 1
- HILAYQUKKYWPJW-UHFFFAOYSA-N 1-dodecylguanidine Chemical compound CCCCCCCCCCCCN=C(N)N HILAYQUKKYWPJW-UHFFFAOYSA-N 0.000 description 1
- LEHNQGSPRXHYRT-UHFFFAOYSA-N 2-dodecyl-1h-imidazole Chemical compound CCCCCCCCCCCCC1=NC=CN1 LEHNQGSPRXHYRT-UHFFFAOYSA-N 0.000 description 1
- 229940099451 3-iodo-2-propynylbutylcarbamate Drugs 0.000 description 1
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 description 1
- SBUKOHLFHYSZNG-UHFFFAOYSA-N 4-dodecyl-2,6-dimethylmorpholine Chemical compound CCCCCCCCCCCCN1CC(C)OC(C)C1 SBUKOHLFHYSZNG-UHFFFAOYSA-N 0.000 description 1
- FEPBITJSIHRMRT-UHFFFAOYSA-N 4-hydroxybenzenesulfonic acid Chemical compound OC1=CC=C(S(O)(=O)=O)C=C1 FEPBITJSIHRMRT-UHFFFAOYSA-N 0.000 description 1
- AWQSAIIDOMEEOD-UHFFFAOYSA-N 5,5-Dimethyl-4-(3-oxobutyl)dihydro-2(3H)-furanone Chemical compound CC(=O)CCC1CC(=O)OC1(C)C AWQSAIIDOMEEOD-UHFFFAOYSA-N 0.000 description 1
- XZOYHFBNQHPJRQ-UHFFFAOYSA-N 7-methyloctanoic acid Chemical compound CC(C)CCCCCC(O)=O XZOYHFBNQHPJRQ-UHFFFAOYSA-N 0.000 description 1
- 241000609240 Ambelania acida Species 0.000 description 1
- 241000228245 Aspergillus niger Species 0.000 description 1
- 241000223678 Aureobasidium pullulans Species 0.000 description 1
- 241000221198 Basidiomycota Species 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- 241001515917 Chaetomium globosum Species 0.000 description 1
- GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical compound C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 description 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 1
- JYFHYPJRHGVZDY-UHFFFAOYSA-N Dibutyl phosphate Chemical compound CCCCOP(O)(=O)OCCCC JYFHYPJRHGVZDY-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 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
- DYMNZCGFRHLNMT-UHFFFAOYSA-N Glyodin Chemical compound CC(O)=O.CCCCCCCCCCCCCCCCCC1=NCCN1 DYMNZCGFRHLNMT-UHFFFAOYSA-N 0.000 description 1
- 239000005795 Imazalil Substances 0.000 description 1
- SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 241001674251 Serpula lacrymans Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- BAZMYXGARXYAEQ-UHFFFAOYSA-N alpha-ethyl valeric acid Chemical compound CCCC(CC)C(O)=O BAZMYXGARXYAEQ-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000010905 bagasse Substances 0.000 description 1
- LJOZMWRYMKECFF-UHFFFAOYSA-N benodanil Chemical compound IC1=CC=CC=C1C(=O)NC1=CC=CC=C1 LJOZMWRYMKECFF-UHFFFAOYSA-N 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- BNMJSBUIDQYHIN-UHFFFAOYSA-N butyl dihydrogen phosphate Chemical compound CCCCOP(O)(O)=O BNMJSBUIDQYHIN-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- QQWAGMBIDPBJRR-UHFFFAOYSA-N cyclohexyldiazene Chemical compound N=NC1CCCCC1 QQWAGMBIDPBJRR-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 229960002125 enilconazole Drugs 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 230000002538 fungal effect Effects 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
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 229940083094 guanine derivative acting on arteriolar smooth muscle Drugs 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 238000012432 intermediate storage Methods 0.000 description 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 229960002809 lindane Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- RMIODHQZRUFFFF-UHFFFAOYSA-N methoxyacetic acid Chemical compound COCC(O)=O RMIODHQZRUFFFF-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 150000002780 morpholines Chemical class 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 229960000490 permethrin Drugs 0.000 description 1
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 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
- 238000005507 spraying Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- DYWSVUBJGFTOQC-UHFFFAOYSA-N xi-2-Ethylheptanoic acid Chemical compound CCCCCC(CC)C(O)=O DYWSVUBJGFTOQC-UHFFFAOYSA-N 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
-
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/04—Nitrogen directly attached to aliphatic or cycloaliphatic carbon atoms
-
- 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
- B27K3/16—Inorganic impregnating agents
- B27K3/166—Compounds of phosphorus
-
- 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
-
- 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
-
- 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
-
- 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
- B27K3/52—Impregnating agents containing mixtures of inorganic and organic compounds
Landscapes
- Life Sciences & Earth Sciences (AREA)
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Abstract
Description
Trevirkebeskyttelsesmiddel. Wood preservative.
Foreliggende oppfinnelse vedrører et trevirkebeskyttelsesmiddel på grunnlag av et dimetyl-alkylamin og en syre og anvendelse derav, for beskyttelse av trevirke, spesielt av friskt trevirke, f.eks. friskt oppsaget sagvirke i sagbruk eller nettopp felte trestammer i skogen. The present invention relates to a wood preservative based on a dimethyl alkylamine and an acid and its use, for the protection of wood, especially fresh wood, e.g. freshly sawn timber in a sawmill or just felled tree trunks in the forest.
Det er kjent å anvende dimetylalkylaminer, 2-(metoksy-karbonylamino)benzimidazol (BCM) eller N-tridecyl-2,6-dimetyl-morfolin (tridemorf), f.eks. i form av deres salter, til beskyttelse av trevirke (EP-147 976, DE-3 138 575.3, DE-3 507 4 2 0.5). Virkningen av disse midlene er imidlertid ikke tilfredsstillende. It is known to use dimethylalkylamines, 2-(methoxycarbonylamino)benzimidazole (BCM) or N-tridecyl-2,6-dimethylmorpholine (tridemorph), e.g. in the form of their salts, for the protection of wood (EP-147 976, DE-3 138 575.3, DE-3 507 4 2 0.5). However, the effect of these means is not satisfactory.
Det ble funnet at trevirkebeskyttelsesmidler som inneholder a) et dimetylalkylamin, b) en vannløselig syre og c) en vannuløselig syre eller BCM eller c) en vannuløselig syre og 2-(metoksykarbonylamino)-benzimidazol, bortsett fra en blanding av N-tridecyl-2,6-dimetylmorfolin, dimetyl-C12-alkylamin, etoksylert nonylfenol (9 etylenoksyd pr. fenol), propylenglykol, fluorborsyre, fosforsyre, isooktansyre og vann, har en svært god virkning mot treparasitter, spesielt mot sopp, som er bedre enn virkningen av de kjente trevirkebeskyttelsesmidlene. De nye trevirkebeskyttelsesmidlene er vannløselige. De anvendes i form av vandige impregnerings-løsninger som fremstilles fra trevirkebeskyttelsesmidlene (konsentratene) ved fortynning med vann. Den foreliggende oppfinnelsen omfatter såvel konsentratene som også de fortynnede vandige løsningene (impregnerings-løsningene) som kan fremstilles derav ved fortynning med vann. De nye trevirkebeskyttelsesmidlene egner seg til beskyttelse av trevirke, spesielt av friskt trevirke, slik som det forekommer f.eks. som friskt oppsaget trevirke i sagbruk eller som nettopp felte trestammer i skogen. It was found that wood preservatives containing a) a dimethylalkylamine, b) a water-soluble acid and c) a water-insoluble acid or BCM or c) a water-insoluble acid and 2-(methoxycarbonylamino)-benzimidazole, except for a mixture of N-tridecyl-2 ,6-dimethylmorpholine, dimethyl-C12-alkylamine, ethoxylated nonylphenol (9 ethylene oxide per phenol), propylene glycol, fluoroboric acid, phosphoric acid, isooctanoic acid and water, have a very good effect against wood parasites, especially against fungi, which is better than the effect of the known wood preservatives. The new wood preservatives are water-soluble. They are used in the form of aqueous impregnation solutions that are produced from the wood preservatives (concentrates) by dilution with water. The present invention includes the concentrates as well as the diluted aqueous solutions (impregnation solutions) which can be prepared from them by dilution with water. The new wood preservatives are suitable for the protection of wood, especially of fresh wood, as occurs e.g. as freshly felled timber in a sawmill or as just felled tree trunks in the forest.
Et dimetylalkylamin er et N,N-dimetyl-N-alkylamin med en alkylrest som inneholder eksempelvis 6 til 20 C-atomer. Dimetylalkylaminer med 12 til 14 C-atomer i alkylresten blir foretrukket. Ved siden av de rene dimetylalkylaminene kan også anvendes blandinger, f.eks. blandinger av dimetyl-C12-alkylamin og dimetyl-C14-alkylamin (dimetylalkyl (C12/C14-aiuin) . A dimethylalkylamine is an N,N-dimethyl-N-alkylamine with an alkyl residue containing, for example, 6 to 20 carbon atoms. Dimethylalkylamines with 12 to 14 C atoms in the alkyl residue are preferred. In addition to the pure dimethylalkylamines, mixtures can also be used, e.g. mixtures of dimethyl-C12-alkylamine and dimethyl-C14-alkylamine (dimethylalkyl (C12/C14-aiuin) .
En vannløselig syre er eksempelvis en vannløselig uorganisk syre, f.eks. en syre av fosfor, spesielt fosfonsyre (H3PO3) , fosfinsyre (H3P02) , sure fosforsyreestere (f.eks. fosforsyre-mono- (eller -di)-alkylester, eksempelvis fosfor-syremonobutylester, fosforsyre-di-butylester), fosfonsyre-mono-alkylester eller en syre av svovel, f.eks. en sulfonsyre, eksempelvis benzo 1-mono- (eller -di)-sulfonsyre, sulfaminsyre, 4-fenolsulfonsyre. Dessuten en organisk C2-C4-karboksyl-syre, f.eks. monokarboksylsyre, eksempelvis eddiksyre, propionsyre, metoksyeddiksyre, melkesyre, glykolsyre eller polykarboksylsyre, f.eks. fumarsyre, citronsyre, maleinsyre. A water-soluble acid is, for example, a water-soluble inorganic acid, e.g. an acid of phosphorus, especially phosphonic acid (H3PO3), phosphinic acid (H3P02), acidic phosphoric acid esters (e.g. phosphoric acid mono- (or -di)-alkyl ester, e.g. phosphoric acid monobutyl ester, phosphoric acid di-butyl ester), phosphonic acid mono -alkyl ester or an acid of sulphur, e.g. a sulfonic acid, for example benzo 1-mono- (or -di)-sulfonic acid, sulfamic acid, 4-phenolsulfonic acid. Also, an organic C2-C4 carboxylic acid, e.g. monocarboxylic acid, for example acetic acid, propionic acid, methoxyacetic acid, lactic acid, glycolic acid or polycarboxylic acid, e.g. fumaric acid, citric acid, maleic acid.
En vannuløselig syre er f.eks. en alifatisk C5-C20-karboksylsyre, eksempelvis en monokarboksylsyre, heksansyre, heptansyre, oktansyre, nonansyre, dekansyre, 2-etylpentansyre, 2-etylheksansyre, 2-etylheptansyre, isooktansyre, isononan-syre, versatikksyrér (sterkt forgrenede monokarbokylsyrer), eller en dikarbokylsyre, f.eks. dekandikarboksylsyre. A water-insoluble acid is e.g. an aliphatic C5-C20 carboxylic acid, for example a monocarboxylic acid, hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, 2-ethylpentanoic acid, 2-ethylhexanoic acid, 2-ethylheptanoic acid, isooctanoic acid, isononanoic acid, versatic acids (highly branched monocarboxylic acids), or a dicarboxylic acid , e.g. decane carboxylic acid.
Syrene kan også anvendes i form av sine salter, f.eks. dimetylalkylaminsaltene. De BCM inneholdende midlene kan også ved siden av den vannløselige syren dessuten inneholde en vannuløselig syre. The acids can also be used in the form of their salts, e.g. the dimethylalkylamine salts. The BCM-containing agents can also contain a water-insoluble acid in addition to the water-soluble acid.
Trevirkebeskyttelsesmidlene er blandbare med vann, danner klare løsninger med vann og har i den vanlige anvendelses-konsentrasjonen (0,5 til 10,0 vekt-%, beregnet på konsen-tratet), en pH-verdi lavere enn 7,0 ved utelukkende anvendelse av dimetylalkylamin, ved blandinger av dimetylalkylamin med tridemorf, en pH-verdi lavere enn 6, og ved blandinger av dimetylalkylamin med BCM, en pH-verdi lavere enn 3,5. De fremstilles ved blanding av de enkelte komponentene med hverandre. The wood preservatives are miscible with water, form clear solutions with water and, in the usual application concentration (0.5 to 10.0% by weight, calculated on the concentrate), have a pH value lower than 7.0 when used exclusively of dimethylalkylamine, for mixtures of dimethylalkylamine with tridemorph, a pH value lower than 6, and for mixtures of dimethylalkylamine with BCM, a pH value lower than 3.5. They are produced by mixing the individual components with each other.
Trevirkebeskyttelsesmidlene (konsentratene) er mer eller mindre viskøse løsninger, med en viskositet som kan reduseres ved tilsetning av polare løsningsmidler. Som polare løsnings-midler kan anvendes f.eks. dimetylformamid, dietylformamid, N-metylpyrrolidon, dimetylsulfoksyd, glykoler, polyglykoler, glykoleter, glykoleteracetater og alkoholer. I disse tilfellene foreligger BCM-saltet for det meste i pastaform. The wood protection agents (concentrates) are more or less viscous solutions, with a viscosity that can be reduced by adding polar solvents. Polar solvents can be used, e.g. dimethylformamide, diethylformamide, N-methylpyrrolidone, dimethylsulfoxide, glycols, polyglycols, glycol ethers, glycol ether acetates and alcohols. In these cases, the BCM salt is mostly present in paste form.
Konsentratene inneholder vanligvis (vekt-%). The concentrates usually contain (% by weight).
hvorved summen alltid skal være 100 vekt-%. whereby the sum must always be 100% by weight.
Blandingsforholdet (vekt-deler) av BCM til dimetylalkylamin ligger f.eks. mellom 1:50 til 2:1, fortrinnsvis 1:20 til 1:2. The mixing ratio (parts by weight) of BCM to dimethylalkylamine is e.g. between 1:50 to 2:1, preferably 1:20 to 1:2.
Dessuten kan vann være tilstede, som f.eks. inneholdes i de handelsvanlige formene av syrene. I tilleg kan tilsettes: fuktemidler, korrosjonsinhibitorer, fargestoffer og eventuelt bindemiddel. In addition, water may be present, such as e.g. contained in the commercially available forms of the acids. In addition, the following can be added: wetting agents, corrosion inhibitors, dyes and possibly a binder.
For å forbedre virkningsbredden av trevirkebeskyttelsesmidlene, kan de dessuten også inneholde nitrogenholdige organiske fungicider, f.eks. ytterligere morfolinderivater, som f.eks. fenpropemorf, aldimorf; guanidinderivater, som f.eks. dodecylguanidin, klorheksadin, guazatin, f.eks. imidazolderivater, f.eks. imazalil, dodecylimidazol, glyodin; pyrimidinderivater, f.eks. heksatidin, kvartære ammonium-forbindelser, f.eks. N-dodecylpyridinklorid. Dessuten kan andre fungicider anvendes i tillegg, som f.eks. 2-(tiocyan-metyltio)benzotiazol, 3-jod-2-propynylbutylkarbamat, 2-(4-tiazolyl)benzimidazol, vannløselige salter (f.eks. kalium-saltet) av N-cykloheksyl'diazeniumdioksydet. In order to improve the effectiveness of the wood preservatives, they can also contain nitrogen-containing organic fungicides, e.g. further morpholine derivatives, such as e.g. fenpropemorph, aldimorph; guanidine derivatives, such as dodecylguanidine, chlorhexadine, guazatin, e.g. imidazole derivatives, e.g. imazalil, dodecylimidazole, glyodin; pyrimidine derivatives, e.g. hexatidine, quaternary ammonium compounds, e.g. N-dodecylpyridine chloride. Furthermore, other fungicides can be used in addition, such as e.g. 2-(Thiocyanomethylthio)benzothiazole, 3-iodo-2-propynylbutylcarbamate, 2-(4-thiazolyl)benzimidazole, water soluble salts (e.g. the potassium salt) of N-cyclohexyldiazenium dioxide.
Også andre fungicider, som f.eks. furmecykloks eller benodanil, eller insekticider, som lindan eller permetrin, kan tilsettes til formuleringene, de må eventuelt innarbeides under tilsetning av emulgatorer, f.eks. etoksylerte nonyl-fenoler. Also other fungicides, such as e.g. furmecyclox or benodanil, or insecticides, such as lindane or permethrin, can be added to the formulations, they must possibly be incorporated with the addition of emulsifiers, e.g. ethoxylated nonyl phenols.
Anvendelsen av beskyttelsesmiddelet for treverket kan, alt etter hvor utsatt treverket er, foregå f.eks.: The application of the protective agent for the wood can, depending on how exposed the wood is, take place, for example:
a) ved påsprøytning av treverket med oppløsningen, a) by spraying the wood with the solution,
b) ved neddykking av treverket i oppløsningen, b) by immersing the wood in the solution,
c) ved impregnering av treverket ved hjelp av c) by impregnating the wood using
trykkforskjeller, pressure differences,
f.eks. kjeletrykk- eller dobbelvakuumimpregnering, e.g. boiler pressure or double vacuum impregnation,
d) ved påstrykning av treverket. d) when ironing the wood.
Ved følgeprodukter av tre, f.eks. oppsaget treverk, In the case of secondary products made of wood, e.g. reclaimed wood,
cellestoff, såvel som videre tekniske produkter eller også celluloseholdige materialer som utsettes for soppangrep, f.eks. mellomprodukter ved papirfremstillingen, treaktige ettårsplanter (bagasse, raps) må anvendelsen tilpasses til de tekniske mulighetene. cell material, as well as further technical products or also cellulose-containing materials which are exposed to fungal attack, e.g. intermediate products in paper production, woody annual plants (bagasse, rapeseed), the application must be adapted to the technical possibilities.
Virkningen av midlene på trevirkebeskyttelsesområdet omfatter eksempelvis: The effect of the funds in the wood protection area includes, for example:
a) muggsopp (f.eks. aspergillus niger), a) molds (e.g. aspergillus niger),
b) forråtnelsessopp (f.eks. chaetomium globosum), b) decay fungi (e.g. chaetomium globosum),
c) blåsopp (f.eks. pullularia pullulans), c) blue fungus (e.g. pullularia pullulans),
d) treødeleggende basidiomyceter (f.eks. serpula lacrymans), spesielt er virkningen svært god mot blåsopp. d) wood-destroying basidiomycetes (e.g. serpula lacrymans), especially the effect is very good against blue fungus.
Trevirkebeskyttelsesmidlene har en svært god fungicid virkning, som det fremgår av følgende forsøk. The wood preservatives have a very good fungicidal effect, as can be seen from the following experiments.
Til forsøkene ble anvendt saftfriske, nettopp oppsagede stykker av ytterved av bartre med målene 200 x 50 x 15 mm, som var dypfryst til forsøkende begynte. For the experiments fresh, freshly sawn pieces of coniferous outer wood measuring 200 x 50 x 15 mm were used, which were deep-frozen until the experiments began.
Etter opptining, (omlag 6 timer) ble trestykkene dykket ned i de løsningene som skulle anvendes i ca. 10 sekunder, stillet svakt på skrå for avdrypping og etter en mellomlagring på ca. 24 timer under normale klimabetingelser, plassert i forsøkslandskapet. Med de enkelte forsøksløsningene ble 10 prøvebrett impregnert av gangen på den ovenfor beskrevne måten. Kontrolltrestykker uten impregnering ble neddykket i rent vann. After thawing, (approx. 6 hours), the pieces of wood were immersed in the solutions to be used for approx. 10 seconds, slightly tilted for draining and after an intermediate storage of approx. 24 hours under normal climate conditions, placed in the experimental landscape. With the individual test solutions, 10 test boards were impregnated at a time in the manner described above. Control pieces of wood without impregnation were immersed in clean water.
Som prøvelandskap ble valgt ut en skyggefull eng, der gressvollen ble snauklippet før utleggingen av prøvestykkene. Prøvestykkene ble lagt ut på to kunststoffskinner i en høyde A shady meadow was selected as the test landscape, where the grass embankment was cut short before laying out the test pieces. The test pieces were laid out on two plastic rails at one height
av ca. 1 cm over gressvollen. of approx. 1 cm above the grass embankment.
De prøvebrettene som var utsatt for den ytre påvirkningen (regn) ble prøvet etter 2 mnd. (august/september). The test boards that were exposed to the external influence (rain) were tested after 2 months. (August/September).
Den fungicide virkningen ble klassifisert i fire kate-gorier på grunn av den opptredende fargingen og forandringen av treoverflaten: The fungicidal action was classified into four categories due to the occurring staining and change of the wood surface:
0 ingen vekst 0 no growth
+ svak punktvis overflatevekst + weak punctate surface growth
++ sterkere punktvis vekst ++ stronger point-wise growth
+++ store flater inntil fullstendig bevokst. +++ large areas until completely overgrown.
Sammenligningseksempel: Comparison example:
50, 00% dimetylalkylamin (C12/C1A) 50.00% Dimethylalkylamine (C12/C1A)
17,50% fosfonsyre 17.50% phosphonic acid
22,50% propylenglykol 22.50% propylene glycol
Sammenligningseksempel: 50,00% tridemorf 3 0,00% fosfonsyre 20,00% propylenglykol Comparative example: 50.00% tridemorph 3 0.00% phosphonic acid 20.00% propylene glycol
Eksempel 1 (ifølge oppfinnelsen): Example 1 (according to the invention):
Eksempel 2: Example 2:
30,00% dimetylalkylamin (C12/Cu) 2 0,00% tridemorf 25,00% fosfonsyre 25,00% propylenglykol 30.00% dimethylalkylamine (C12/Cu) 2 0.00% tridemorph 25.00% phosphonic acid 25.00% propylene glycol
Eksempel 3: Example 3:
35,00% dimetylalkylamin (C12/Cu) 35.00% dimethylalkylamine (C12/Cu)
20,00% tridemorf 20.00% tridemorph
10,00% isooktansyre 10.00% isooctanoic acid
35,00% melkesyre 85% (15% vann) 35.00% lactic acid 85% (15% water)
Sammenligning: Comparison:
25,00% 2-(metoksykarbonylamino)-benzimidazol 37,50% fosfonsyre 25.00% 2-(methoxycarbonylamino)-benzimidazole 37.50% phosphonic acid
37,50% vann 37.50% water
Eksempel 4: Example 4:
Sammenligningseksempel BCM: Comparison example BCM:
50% 2-(metoksy-karbonylamino)-benzimidazol 50% sulfaminsyre 50% 2-(methoxy-carbonylamino)-benzimidazole 50% sulfamic acid
(omsatt i vakuum-knamaskin) (processed in a vacuum kneader)
Eksempel 5 (ifølge oppfinnelsen): Example 5 (according to the invention):
Eksempel 6: Example 6:
Alle prøvetrestykkene uten behandling var bevokst og farget med blåsopp (+++). All the test pieces of wood without treatment were overgrown and stained with blue fungus (+++).
Ytterligere en blanding med god fungicid virkning er følgende blanding: Another mixture with good fungicidal effect is the following mixture:
Claims (5)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19873736298 DE3736298A1 (en) | 1987-10-27 | 1987-10-27 | WOOD PRESERVATIVES |
Publications (4)
Publication Number | Publication Date |
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NO884758D0 NO884758D0 (en) | 1988-10-26 |
NO884758L NO884758L (en) | 1989-04-28 |
NO176088B true NO176088B (en) | 1994-10-24 |
NO176088C NO176088C (en) | 1995-02-01 |
Family
ID=6339153
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO884758A NO176088C (en) | 1987-10-27 | 1988-10-26 | Wood preservative and its use |
Country Status (10)
Country | Link |
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EP (2) | EP0316602B1 (en) |
AT (2) | ATE90611T1 (en) |
AU (1) | AU605639B2 (en) |
CA (1) | CA1327428C (en) |
DE (3) | DE3736298A1 (en) |
ES (2) | ES2067109T3 (en) |
FI (1) | FI98797C (en) |
NO (1) | NO176088C (en) |
NZ (1) | NZ226721A (en) |
PT (1) | PT88855B (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3839640A1 (en) * | 1988-11-24 | 1990-05-31 | Wolman Gmbh Dr | WOOD PRESERVATIVES |
DE3918978A1 (en) * | 1989-06-10 | 1990-12-13 | Wolman Gmbh Dr | MIXING FOR WOOD PROTECTION |
DE4009740A1 (en) * | 1990-03-27 | 1991-10-02 | Desowag Materialschutz Gmbh | MEDIUM OR CONCENTRATE FOR PROTECTING SAWN WOOD AGAINST WOOD-MOLDING MUSHROOMS |
DE4441672A1 (en) * | 1994-11-23 | 1996-05-30 | Basf Ag | Wood preservatives |
DE19517811C2 (en) * | 1995-05-17 | 1999-02-25 | Baden Chemie Gmbh | Use of a coating material to reduce or avoid the release of biocides |
EP1071331A4 (en) * | 1998-04-17 | 2004-12-29 | Matter Smiths Holdings Ltd | A biocidal composition containing phosphite ions |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3138575A1 (en) * | 1981-09-28 | 1983-04-07 | Basf Ag, 6700 Ludwigshafen | FUNGICIDE |
GB8333228D0 (en) * | 1983-12-13 | 1984-01-18 | Hicksons Timber Products Ltd | Antifungal compositions |
DE3502939A1 (en) * | 1985-01-30 | 1986-07-31 | Dr. Wolman Gmbh, 7573 Sinzheim | FUNGICIDE AGENT |
DE3507420A1 (en) * | 1985-03-02 | 1986-09-04 | Basf Ag, 6700 Ludwigshafen | WOOD PRESERVATIVES |
DE3605007A1 (en) * | 1986-02-18 | 1987-08-20 | Wolman Gmbh Dr | SALT OF A SUBSTITUTED MORPHOLIN WITH FLUOROBORIC ACID AND WOOD PRESERVATIVE |
DE3613254A1 (en) * | 1986-04-19 | 1987-10-22 | Wolman Gmbh Dr | WOOD PROTECTIVE AGENT WITH DIMETHYL ALKYLAMINE AND BORIC ACID |
-
1987
- 1987-10-27 DE DE19873736298 patent/DE3736298A1/en not_active Withdrawn
-
1988
- 1988-10-19 ES ES91115260T patent/ES2067109T3/en not_active Expired - Lifetime
- 1988-10-19 EP EP88117433A patent/EP0316602B1/en not_active Expired - Lifetime
- 1988-10-19 ES ES198888117433T patent/ES2040810T3/en not_active Expired - Lifetime
- 1988-10-19 DE DE3852704T patent/DE3852704D1/en not_active Expired - Fee Related
- 1988-10-19 AT AT88117433T patent/ATE90611T1/en not_active IP Right Cessation
- 1988-10-19 AT AT91115260T patent/ATE116591T1/en active
- 1988-10-19 EP EP91115260A patent/EP0466206B1/en not_active Expired - Lifetime
- 1988-10-19 DE DE8888117433T patent/DE3881831D1/en not_active Expired - Lifetime
- 1988-10-20 FI FI884848A patent/FI98797C/en not_active IP Right Cessation
- 1988-10-25 CA CA000581222A patent/CA1327428C/en not_active Expired - Lifetime
- 1988-10-26 AU AU24347/88A patent/AU605639B2/en not_active Expired
- 1988-10-26 NO NO884758A patent/NO176088C/en not_active IP Right Cessation
- 1988-10-26 PT PT88855A patent/PT88855B/en not_active IP Right Cessation
- 1988-10-26 NZ NZ226721A patent/NZ226721A/en unknown
Also Published As
Publication number | Publication date |
---|---|
FI98797B (en) | 1997-05-15 |
FI884848A0 (en) | 1988-10-20 |
EP0466206B1 (en) | 1995-01-04 |
ATE90611T1 (en) | 1993-07-15 |
ES2040810T3 (en) | 1993-11-01 |
DE3881831D1 (en) | 1993-07-22 |
AU605639B2 (en) | 1991-01-17 |
EP0316602A3 (en) | 1990-09-12 |
NZ226721A (en) | 1990-01-29 |
CA1327428C (en) | 1994-03-08 |
ES2067109T3 (en) | 1995-03-16 |
NO884758D0 (en) | 1988-10-26 |
FI98797C (en) | 1997-08-25 |
DE3736298A1 (en) | 1989-05-11 |
PT88855B (en) | 1993-01-29 |
EP0466206A1 (en) | 1992-01-15 |
NO884758L (en) | 1989-04-28 |
AU2434788A (en) | 1989-04-27 |
EP0316602A2 (en) | 1989-05-24 |
FI884848A (en) | 1989-04-28 |
EP0316602B1 (en) | 1993-06-16 |
NO176088C (en) | 1995-02-01 |
DE3852704D1 (en) | 1995-02-16 |
ATE116591T1 (en) | 1995-01-15 |
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