CH637003A5 - Method of controlling weeds - Google Patents
Method of controlling weeds Download PDFInfo
- Publication number
- CH637003A5 CH637003A5 CH62379A CH62379A CH637003A5 CH 637003 A5 CH637003 A5 CH 637003A5 CH 62379 A CH62379 A CH 62379A CH 62379 A CH62379 A CH 62379A CH 637003 A5 CH637003 A5 CH 637003A5
- Authority
- CH
- Switzerland
- Prior art keywords
- foam
- acid
- water
- weeds
- weight
- Prior art date
Links
- 241000196324 Embryophyta Species 0.000 title claims description 24
- 238000000034 method Methods 0.000 title claims description 12
- 239000006260 foam Substances 0.000 claims description 23
- 230000002363 herbicidal effect Effects 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 13
- 239000004480 active ingredient Substances 0.000 claims description 11
- 239000000243 solution Substances 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 10
- 239000004094 surface-active agent Substances 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims description 3
- HXKWSTRRCHTUEC-UHFFFAOYSA-N 2,4-Dichlorophenoxyaceticacid Chemical compound OC(=O)C(Cl)OC1=CC=C(Cl)C=C1 HXKWSTRRCHTUEC-UHFFFAOYSA-N 0.000 claims description 3
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 claims description 3
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims description 3
- 238000005187 foaming Methods 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 244000025254 Cannabis sativa Species 0.000 claims 1
- 244000038559 crop plants Species 0.000 claims 1
- 230000006378 damage Effects 0.000 claims 1
- 239000000839 emulsion Substances 0.000 claims 1
- 239000000725 suspension Substances 0.000 claims 1
- 235000013311 vegetables Nutrition 0.000 claims 1
- 239000004563 wettable powder Substances 0.000 claims 1
- -1 2-chloroalyl-N Chemical class 0.000 description 11
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 8
- 150000007513 acids Chemical class 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000005574 MCPA Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-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
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 229960001701 chloroform Drugs 0.000 description 3
- 125000002147 dimethylamino group Chemical class [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 3
- SMYMJHWAQXWPDB-UHFFFAOYSA-N (2,4,5-trichlorophenoxy)acetic acid Chemical compound OC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl SMYMJHWAQXWPDB-UHFFFAOYSA-N 0.000 description 2
- 239000003559 2,4,5-trichlorophenoxyacetic acid Substances 0.000 description 2
- MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 101000742062 Bos taurus Protein phosphatase 1G Proteins 0.000 description 2
- YPQSPODHFDGVAC-UHFFFAOYSA-N Butyl heptanoate Chemical compound CCCCCCC(=O)OCCCC YPQSPODHFDGVAC-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ZLSWBLPERHFHIS-UHFFFAOYSA-N Fenoprop Chemical compound OC(=O)C(C)OC1=CC(Cl)=C(Cl)C=C1Cl ZLSWBLPERHFHIS-UHFFFAOYSA-N 0.000 description 2
- XGEGHDBEHXKFPX-UHFFFAOYSA-N N-methylthiourea Natural products CNC(N)=O XGEGHDBEHXKFPX-UHFFFAOYSA-N 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- RGXWDWUGBIJHDO-UHFFFAOYSA-N ethyl decanoate Chemical compound CCCCCCCCCC(=O)OCC RGXWDWUGBIJHDO-UHFFFAOYSA-N 0.000 description 2
- TVQGDYNRXLTQAP-UHFFFAOYSA-N ethyl heptanoate Chemical compound CCCCCCC(=O)OCC TVQGDYNRXLTQAP-UHFFFAOYSA-N 0.000 description 2
- MMXKVMNBHPAILY-UHFFFAOYSA-N ethyl laurate Chemical compound CCCCCCCCCCCC(=O)OCC MMXKVMNBHPAILY-UHFFFAOYSA-N 0.000 description 2
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
- XXOYNJXVWVNOOJ-UHFFFAOYSA-N fenuron Chemical compound CN(C)C(=O)NC1=CC=CC=C1 XXOYNJXVWVNOOJ-UHFFFAOYSA-N 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- YRHYCMZPEVDGFQ-UHFFFAOYSA-N methyl decanoate Chemical compound CCCCCCCCCC(=O)OC YRHYCMZPEVDGFQ-UHFFFAOYSA-N 0.000 description 2
- UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 description 2
- ZAZKJZBWRNNLDS-UHFFFAOYSA-N methyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OC ZAZKJZBWRNNLDS-UHFFFAOYSA-N 0.000 description 2
- XGEGHDBEHXKFPX-NJFSPNSNSA-N methylurea Chemical compound [14CH3]NC(N)=O XGEGHDBEHXKFPX-NJFSPNSNSA-N 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 239000003380 propellant Substances 0.000 description 2
- 150000003918 triazines Chemical class 0.000 description 2
- WJTCHBVEUFDSIK-NWDGAFQWSA-N (2r,5s)-1-benzyl-2,5-dimethylpiperazine Chemical compound C[C@@H]1CN[C@@H](C)CN1CC1=CC=CC=C1 WJTCHBVEUFDSIK-NWDGAFQWSA-N 0.000 description 1
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- RLPSARLYTKXVSE-UHFFFAOYSA-N 1-(1,3-thiazol-5-yl)ethanamine Chemical compound CC(N)C1=CN=CS1 RLPSARLYTKXVSE-UHFFFAOYSA-N 0.000 description 1
- HNAGHMKIPMKKBB-UHFFFAOYSA-N 1-benzylpyrrolidine-3-carboxamide Chemical compound C1C(C(=O)N)CCN1CC1=CC=CC=C1 HNAGHMKIPMKKBB-UHFFFAOYSA-N 0.000 description 1
- CLWAXFZCVYJLLM-UHFFFAOYSA-N 1-chlorohexadecane Chemical compound CCCCCCCCCCCCCCCCCl CLWAXFZCVYJLLM-UHFFFAOYSA-N 0.000 description 1
- VUQPJRPDRDVQMN-UHFFFAOYSA-N 1-chlorooctadecane Chemical compound CCCCCCCCCCCCCCCCCCCl VUQPJRPDRDVQMN-UHFFFAOYSA-N 0.000 description 1
- WLXGQMVCYPUOLM-UHFFFAOYSA-N 1-hydroxyethanesulfonic acid Chemical compound CC(O)S(O)(=O)=O WLXGQMVCYPUOLM-UHFFFAOYSA-N 0.000 description 1
- IONYGGJUUJFXJK-UHFFFAOYSA-N 2,3,4,5,6-pentachlorobenzoic acid Chemical class OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IONYGGJUUJFXJK-UHFFFAOYSA-N 0.000 description 1
- XZIDTOHMJBOSOX-UHFFFAOYSA-N 2,3,6-TBA Chemical compound OC(=O)C1=C(Cl)C=CC(Cl)=C1Cl XZIDTOHMJBOSOX-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 description 1
- 239000002794 2,4-DB Substances 0.000 description 1
- YOYAIZYFCNQIRF-UHFFFAOYSA-N 2,6-dichlorobenzonitrile Chemical compound ClC1=CC=CC(Cl)=C1C#N YOYAIZYFCNQIRF-UHFFFAOYSA-N 0.000 description 1
- IUQJDHJVPLLKFL-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)acetate;dimethylazanium Chemical compound CNC.OC(=O)COC1=CC=C(Cl)C=C1Cl IUQJDHJVPLLKFL-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-DOMIDYPGSA-N 2-(2,4-dichlorophenoxy)acetic acid Chemical compound OC(=O)[14CH2]OC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-DOMIDYPGSA-N 0.000 description 1
- PKAUICCNAWQPAU-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)acetic acid;n-methylmethanamine Chemical compound CNC.CC1=CC(Cl)=CC=C1OCC(O)=O PKAUICCNAWQPAU-UHFFFAOYSA-N 0.000 description 1
- PTCHZQXIZPMPNB-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)benzoic acid Chemical compound CC1=CC(Cl)=CC=C1OC1=CC=CC=C1C(O)=O PTCHZQXIZPMPNB-UHFFFAOYSA-N 0.000 description 1
- NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical compound CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
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- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 description 1
- JDRFUUBRGGDEIZ-UHFFFAOYSA-N 3,6-dichloro-2-methoxybenzoate;dimethylazanium Chemical compound CNC.COC1=C(Cl)C=CC(Cl)=C1C(O)=O JDRFUUBRGGDEIZ-UHFFFAOYSA-N 0.000 description 1
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- AMEMLELAMQEAIA-UHFFFAOYSA-N 6-(tert-butyl)thieno[3,2-d]pyrimidin-4(3H)-one Chemical compound N1C=NC(=O)C2=C1C=C(C(C)(C)C)S2 AMEMLELAMQEAIA-UHFFFAOYSA-N 0.000 description 1
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- PYGXAGIECVVIOZ-UHFFFAOYSA-N Dibutyl decanedioate Chemical compound CCCCOC(=O)CCCCCCCCC(=O)OCCCC PYGXAGIECVVIOZ-UHFFFAOYSA-N 0.000 description 1
- 239000005504 Dicamba Substances 0.000 description 1
- VOWAEIGWURALJQ-UHFFFAOYSA-N Dicyclohexyl phthalate Chemical compound C=1C=CC=C(C(=O)OC2CCCCC2)C=1C(=O)OC1CCCCC1 VOWAEIGWURALJQ-UHFFFAOYSA-N 0.000 description 1
- 239000005630 Diquat Substances 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 description 1
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- 150000001298 alcohols Chemical class 0.000 description 1
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- 229910052783 alkali metal Inorganic materials 0.000 description 1
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- ONSKGPPTXAPQON-UHFFFAOYSA-N fluoromethane dihydrochloride Chemical compound Cl.Cl.FC ONSKGPPTXAPQON-UHFFFAOYSA-N 0.000 description 1
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- 238000010438 heat treatment Methods 0.000 description 1
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- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
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- 150000002576 ketones Chemical class 0.000 description 1
- ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 description 1
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- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical compound FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 description 1
- 235000019407 octafluorocyclobutane Nutrition 0.000 description 1
- PSXNDMJWRZYVTM-UHFFFAOYSA-N octanoic acid butyl ester Natural products CCCCCCCC(=O)OCCCC PSXNDMJWRZYVTM-UHFFFAOYSA-N 0.000 description 1
- YYZUSRORWSJGET-UHFFFAOYSA-N octanoic acid ethyl ester Natural products CCCCCCCC(=O)OCC YYZUSRORWSJGET-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- SUOONJXHCFVNRL-UHFFFAOYSA-N oxadithiirane Chemical compound O1SS1 SUOONJXHCFVNRL-UHFFFAOYSA-N 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 235000017709 saponins Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 229940029284 trichlorofluoromethane Drugs 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
- A01N39/04—Aryloxy-acetic acids; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/16—Foams
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
-
- 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
Die vorliegende Erfindung betrifft nun ein Verfahren zur Bekämpfung von Unkraut durch Behandlung mit einem Unkrautbekämpfungsmittel, welches dadurch gekennzeichnet ist, dass man das Unkrautbekämpfungsmittel dem Unkraut in Form von Schaum appliziert, wobei man den Schaum auf einige Blätter der Unkrautpflanze aufträgt. Vorzugsweise betrifft die vorliegende Erfindung ein Verfahren zur Bekämpfung von Winden. The present invention now relates to a method for controlling weeds by treatment with a weed control agent, which is characterized in that the weed control agent is applied to the weeds in the form of a foam, the foam being applied to some leaves of the weed plant. The present invention preferably relates to a method for combating winds.
Erfindungsgemäss wird ein Unkrautbekämpfungsmittel enthaltender wässriger steifer Schaum auf die Blätter der zu vertilgenden Unkräuter mittels einer schaumerzeugenden Apparatur wie eines Sprühgeräts oder einer sogenannten Aerosoldose appliziert. Der im vorliegenden Verfahren verwendbare Schaum haftet an den Blättern während der gan-5 zen Trocknungszeit, so dass das herbizide Mittel nach der Behandlung der Blätter keine grosse Neigung hat, auf die benachbarten Pflanzen oder auf den Boden zu fliessen. According to the invention, an aqueous stiff foam containing weed control agent is applied to the leaves of the weeds to be destroyed by means of a foam-producing apparatus such as a spraying device or a so-called aerosol can. The foam which can be used in the present process adheres to the leaves during the entire drying time, so that after the treatment of the leaves the herbicidal composition has no great tendency to flow onto the neighboring plants or onto the soil.
Vorzugsweise wird der Schaum nur auf zwei bis drei einzelne Blätter jeder Windenpflanze mit Hilfe eines schaumer-10 zeugenden Apparates aufgetragen, dessen Düse ganz nahe an das Blatt gehalten wird. The foam is preferably applied to only two to three individual leaves of each winch plant with the aid of a foaming device, the nozzle of which is held very close to the leaf.
Ein solcher Schaum kann aus beliebigen schaumbildende Mittel enthaltenden Lösungen oder Dispersionen der Wirkstoffe erzeugt werden. Vorzugsweise wird aber der Schaum 15 aus einer wässrigen kolloidalen Lösung der herbiziden Wirk-stoffkomponente(n) und einem schaumbildenden oberflächenaktiven Mittel erhalten. Die Gewichtsgehalte der so erhaltenen Lösung an Wirkstoffkomponente(n) und an oberflächenaktivem Mittel liegen vorzugsweise in derselben 20 Grössenordnung, insbesondere zwischen 1:1 und 1:2. Das ermöglicht die Gestaltung eines molekularen Gerüstes innerhalb des Schaumes, das dem Schaum eine solche Konsistenz verleiht, dass der Schaum während der ganzen Trocknungszeit an den Blättern haftet. Such a foam can be generated from any solutions or dispersions of the active ingredients containing foam-forming agents. However, the foam 15 is preferably obtained from an aqueous colloidal solution of the herbicidal active ingredient (s) and a foam-forming surface-active agent. The weight contents of active ingredient component (s) and of surface-active agent in the solution thus obtained are preferably of the same 20 order of magnitude, in particular between 1: 1 and 1: 2. This enables the design of a molecular framework within the foam, which gives the foam such a consistency that the foam adheres to the leaves during the entire drying time.
25 Das schaumerzeugende Mittel liegt vorzugsweise in Form einer kolloidalen wässerigen, klaren Lösung bzw. Dispersion vor, welche durch Mischung mit Luft oder mit einem Treibgas einen steifen, nichtfliessenden stabilen Schaum bildet. Es enthält vorzugsweise 0,1 bis 5 Gew.-% eines oder 30 mehrerer herbiziden Wirkstoffe(s), 0,2 bis 10 Gew.-% eines oder mehrerer oberflächenaktiven Wirkstoffe(s) (Emulgiermittel und Schaummittel), 95 bis 99,7 Gew.-% flüssiges Trägermittel, das vorzugsweise Wasser ist, und kann noch weitere Bestandteile enthalten, wie zum Beispiel Schaumstabilisa-35 toren, Konservierungsmittel, Korrosionsinhibitoren, Lösungsmittel, Farbstoff(e) und/oder flüssiges Treibmittel. 25 The foam-generating agent is preferably in the form of a colloidal, aqueous, clear solution or dispersion which, when mixed with air or with a propellant, forms a rigid, non-flowing, stable foam. It preferably contains 0.1 to 5% by weight of one or 30 more herbicidal active ingredients (s), 0.2 to 10% by weight of one or more surface-active ingredients (emulsifiers and foaming agents), 95 to 99.7 % By weight of liquid carrier, which is preferably water, and may also contain further constituents, for example foam stabilizers, preservatives, corrosion inhibitors, solvents, dye (s) and / or liquid propellant.
Als herbizide Wirkstoffe können beispielsweise verwendet werden: 3-Amino-l,2,4-triazol, die herbizid wirksamen 40 Derivate von Uracil wie 5-sek-Brom-3-butyl-6-methyluracil und 3-Cyclohexyl-5,6-trimethylenuracil, die herbizid wirksamen Derivate von Harnstoff wie N,N-Dimethyl-N'-phe-nylharnstoff, bis-(2,2,2-Trichlor-l-hydroxyäthyl)-harnstoff, 3-Phenyl-1,1 -dimethylharnstoff, 3-(p-Chlorphenyl)- 1,1-di-45 methylharnstoff, 3-(3,4-Dichlorphenyl)-l,l-dimethylharn-stoff, n-Butyl-3-(3,4-dichlorphenyl)-l-methylharnstoff und 3-m-Nitrophenyl-l,l-dimethylharnstoff; 2,6-Dichlorbenzo-nitril, die Thiocarboalkoxydisulfide wie Thiocarboäthoxydi-sulfid, Thiocarboisopropoxydisulfid und Thiocarbometh-50 oxydisulfid; die Dithiocarbamate wie 2-ChloralIyl-N,N-di-äthyldithiocarbamat, N-Methyldithiocarbamat und Äthyl-N,N-di-n-propylthiocarbamat, die quaternären Salze von Bipyridilium wie das Dibromid von l,l'-Äthylen-2,2'-bipyri-dylen (Dibromid von Diquat) und das Dichlorid von 1,1'-55 Dimethyl-4,4'-bipyridylen (Dichlorid von Paraquat), die 7-Oxabicyclo-(2,2,l)-2,3-heptandicarbonsäure und ihr Dina-triumsalz, die halogenierten Benzoesäuren und ihre Salze oder von diesen Säuren abstammenden Ester, wie Trichlor-benzoe-, Tetrachlorbenzoe-, Pentachlorbenzoesäuren oder 6o das 2-Äthylhexyl-2,3,4,5-tetrachlorbenzoat, die halogenierten Phenoxyalkansäuren wie 2,4-Dichlorphenoxypropion-säure, 2,4-Dichlorphenoxyessigsäure, 2,4,5-Trichlorphen-oxyessigsäure, 2,4,5-Trichlorphenoxypropionsäure, 2-Me-thyl-4-chlorphenoxypropionsäure, 2,4-Dichlorphenoxybut-65 tersäure und 2-Methyl-4-chlorphenoxyessigsäure und ihre Salze oder die von diesen Säuren abstammenden Ester und die symmetrischen Triazine wie die 4,6-Diamino-symmetri-schen Triazine. Examples of herbicidal active ingredients which can be used are: 3-amino-1,2,4-triazole, the herbicidally active derivatives of uracil such as 5-sec-bromo-3-butyl-6-methyluracil and 3-cyclohexyl-5,6- trimethyleneuracil, the herbicidally active derivatives of urea such as N, N-dimethyl-N'-phenylurea, bis- (2,2,2-trichloro-l-hydroxyethyl) urea, 3-phenyl-1,1-dimethylurea, 3- (p-chlorophenyl) - 1,1-di-45 methylurea, 3- (3,4-dichlorophenyl) -l, l-dimethylurea, n-butyl-3- (3,4-dichlorophenyl) -l methyl urea and 3-m-nitrophenyl-l, l-dimethyl urea; 2,6-dichlorobenzonitrile, the thiocarboalkoxydisulfides such as thiocarboethoxydisulfide, thiocarboisopropoxydisulfide and thiocarbometh-50 oxydisulfide; the dithiocarbamates such as 2-chloroalyl-N, N-di-ethyldithiocarbamate, N-methyldithiocarbamate and ethyl-N, N-di-n-propylthiocarbamate, the quaternary salts of bipyridilium such as the dibromide of 1,1'-ethylene-2,2 '-bipyridylene (dibromide from Diquat) and the dichloride from 1,1'-55 dimethyl-4,4'-bipyridylene (dichloride from Paraquat), the 7-oxabicyclo- (2.2, l) -2.3 -heptanedicarboxylic acid and its disodium salt, the halogenated benzoic acids and their salts or esters derived from these acids, such as trichlorobenzoic, tetrachlorobenzoic, pentachlorobenzoic acids or 6o the 2-ethylhexyl-2,3,4,5-tetrachlorobenzoate which halogenated Phenoxyalkanoic acids such as 2,4-dichlorophenoxypropionic acid, 2,4-dichlorophenoxyacetic acid, 2,4,5-trichlorophenoxyacetic acid, 2,4,5-trichlorophenoxypropionic acid, 2-methyl-4-chlorophenoxypropionic acid, 2,4-dichlorophenoxybut- 65 teric acid and 2-methyl-4-chlorophenoxyacetic acid and their salts or the esters derived from these acids and the symmetrical triazines such as the 4,6-diamino-symme trian triazines.
Bevorzugte herbizide Wirkstoffe sind aber die Salze und Ester der Säuren der Formel I: Preferred herbicidal active ingredients are the salts and esters of the acids of the formula I:
#T #T
(X) < _ )--I-°-C„H2n1n-C00H • (X) <_) - I- ° -C „H2n1n-C00H •
R R
worin X 1 bis 4 Substituenten, ausgewählt aus Chlor und Brom, R ein Wasserstoffatom oder eine Methyl- oder Meth-oxygruppe, n eine ganze Zahl von 1 bis 3 und m 0 oder die Zahl 1 bedeuten. wherein X is 1 to 4 substituents selected from chlorine and bromine, R is a hydrogen atom or a methyl or methoxy group, n is an integer from 1 to 3 and m is 0 or the number 1.
Die mit diesen Säuren gebildeten Ester stammen vorzugsweise von einem primären oder sekundären Alkanol mit 1 bis 12 Kohlenstoffatomen oder einem Alkoxyalkanol mit insgesamt 3 bis 9 Kohlenstoffatomen ab. The esters formed with these acids preferably derive from a primary or secondary alkanol having 1 to 12 carbon atoms or an alkoxyalkanol having a total of 3 to 9 carbon atoms.
Besonders bevorzugte herbizide Mittel sind aber diejenigen, welche Wirkstoffe der Formel (I) in Form ihrer Alkali-, Amin- oder Ammoniumsalze enthalten. In dieser Gruppe werden ganz besonders die wasserlöslichen Aminsalze, insbesondere die Dimethylaminsalze, folgender Säuren bevorzugt: However, particularly preferred herbicidal compositions are those which contain active compounds of the formula (I) in the form of their alkali metal, amine or ammonium salts. The water-soluble amine salts, in particular the dimethylamine salts, of the following acids are particularly preferred in this group:
2,3,6-Trichlorbenzoesäure, 2,3,6-trichlorobenzoic acid,
3,6-Dichlor-2-methoxybenzoesäure(Dicamba), 3,6-dichloro-2-methoxybenzoic acid (dicamba),
2,4-Dichlorphenoxyessigsäure (2,4-D-Säure), 2,4-dichlorophenoxyacetic acid (2,4-D acid),
4-Chlor-2-methylphenoxyessigsäure, 4-chloro-2-methylphenoxyacetic acid,
2,4,5-Trichlorphenoxyessigsäure, 2,4,5-trichlorophenoxyacetic acid,
2-(2,4-Dichlorphenoxy)-propionsäure, 2- (2,4-dichlorophenoxy) propionic acid,
2-(4-Chlor-2-methylphenoxy)-propionsäure (MCPP-Säure) 2- (4-chloro-2-methylphenoxy) propionic acid (MCPP acid)
2-(2,4,5-Trichlorphenoxy)-propionsäure, 2- (2,4,5-trichlorophenoxy) propionic acid,
4-(2,4-Dichlorphenoxy)-buttersäure, 4- (2,4-dichlorophenoxy) butyric acid,
4-(4-Chlor-2-methylphenoxy)-buttersäureund 4- (4-chloro-2-methylphenoxy) butyric acid and
4-(2,4,5-Trichlorphenoxy)-buttersäure, 4- (2,4,5-trichlorophenoxy) butyric acid,
2-Methyl-4-chlorphenoxybenzoesäure (MCPA-Säure). 2-methyl-4-chlorophenoxybenzoic acid (MCPA acid).
Eine Mischung aus 2,4-D-Säure Dimethylaminsalz und MCPA-Säure Dimethylaminsalz in Gewichtsverhältnissen von 1:2 wird ganz besonders bevorzugt. Auch bevorzugt ist eine Mischung aus 2,4-D-Säure Dimethylaminsalz, MCPP-Säure Dimethylaminsalz und Dicamba Dimethylaminsalz in Gewichtsverhältnis von 10:10:1. A mixture of 2,4-D-acid dimethylamine salt and MCPA acid dimethylamine salt in a weight ratio of 1: 2 is very particularly preferred. A mixture of 2,4-D-acid dimethylamine salt, MCPP acid dimethylamine salt and dicamba dimethylamine salt in a weight ratio of 10: 10: 1 is also preferred.
Als oberflächenaktives Mittel können die üblichen schaumerzeugenden anionischen, vorzugsweise nichtionoge-nen, Mittel verwendet werden wie z.B. Saponine, Seifen, Fettalkoholsulfate, Alkylarylsulfate, Alkylarylsulfonate, Sarcosinate, Salze der Kondensationsprodukte aus gesättigten Fettsäuren mit Hydroxyäthansulfonsäure, Salze von Fettsäuren-Polypeptid-Kondensationsprodukten, Salze der Lauryl-(poly-1 -oxapropen)-oxaäthancarbonsäuren, Salze von sulfatierten Monoglyceriden, Fettalkoholpolyäthylen-glykoläther oder Alkylphenolpolyäthylenglykoläther. The usual foam-producing anionic, preferably nonionic, agents, such as e.g. Saponins, soaps, fatty alcohol sulfates, alkylarylsulfates, alkylarylsulfonates, sarcosinates, salts of the condensation products from saturated fatty acids with hydroxyethanesulfonic acid, salts of fatty acids-polypeptide condensation products, salts of lauryl- (poly-1-oxapropenes) -oxaethane-carboxylated fatty acids, monoglypolyalkenesulfonyl sulfonates of fatty alcohols glycol ether or alkylphenol polyethylene glycol ether.
Das oberflächenaktive Mittel muss gleichzeitig ein sehr gutes Schaumvermögen besitzen und gegebenenfalls die Fähigkeit haben, den oder die herbiziden Wirkstoff(e) aufzulösen. Diese Eigenschaft besitzen vorzugsweise die Mischungen aus mindestens zwei nichtionogenen Emulgatoren und einem anionischen Schaummittel. At the same time, the surface-active agent must have very good foaming power and, if appropriate, the ability to dissolve the herbicidal active ingredient (s). The mixtures of at least two nonionic emulsifiers and an anionic foaming agent preferably have this property.
Ein wichtiges Merkmal der Erfindung besteht darin, dass das schaumerzeugende Mittel den herbiziden Bestandteil und das oberflächenaktive Mittel in Gewichtsverhältnissen zwischen 1:1 und 1:2 enthält. An important feature of the invention is that the foam-generating agent contains the herbicidal component and the surface-active agent in weight ratios between 1: 1 and 1: 2.
Als Treibmittel, die zur Erzeugung eines Schaumes verwendbar sind, sind zu erwähnen Butan, Isobutan, Propan, Dimethyläther, Trichlorfluormethan, Dichloridfluormethan, l,2-Dichlor-l,l,2,2-tetrafluoräthan, Tetrafluormethan und Octafluorcyclobutan. As blowing agents which can be used to produce a foam, mention should be made of butane, isobutane, propane, dimethyl ether, trichlorofluoromethane, dichloride fluoromethane, 1,2-dichloro-1,1,2,2-tetrafluoroethane, tetrafluoromethane and octafluorocyclobutane.
Das flüssige Trägermittel besteht vorzugsweise aus Wasser. Es kann aber auch organische Lösungsmittel enthalten, The liquid carrier preferably consists of water. But it can also contain organic solvents
637 003 637 003
z.B. niedere Alkohole wie Methylalkohol, Äthylalkohol oder Äthoxyäthanol und Methoxyäthanol, Isopropylalko-hol, Ketone wie Aceton, Methyläthylketon und Cyclohexa-non, aromatische Kohlenwasserstoffe wie Tetrahydronaph-thalin, aliphatische Kohnenwasserstoffe wie Kerosin, chlorierte Kohlenwasserstoffe wie Dichlormethan, Trichlor-methane, Trichloräthylen und Perchloräthylen, sauerstoffhaltige heterocyclische Verbindungen wie Dioxan, aliphatische Carbonsäureamide wie Dimethylformamid und Di-methylacetamid und Ester, die aus Alkansäuren und Al-kanolen gebildet sind, wobei diese insgesamt zwischen 3 und 15 Kohlenstoffatome aufweisen, wie Methylacetat, Butylace-tat, Amylacetat, Äthylpropionat, Äthylbutyrat, Amylbuty-rat, Äthylheptanoat, Butylheptanoat, Heptylhaptanoat, Äthylcaprylat, Methylcaprat, Äthylcaprat, Methyllaurat, Äthyllaurat, Isopropyllaurat und Methylmyristat, Dimethyl-sulfoxid, Mineralöle, Pflanzenöle, Tieröle und Flüssigkeiten die im allgemeinen zum Plastifizieren von polymeren Harzen verwendet werden, wie im besonderen Chlorhexadecan, Chloroctadecan, Dioctyladipat, Dibutylsebacat, Dioctyl-sebacat, Dioctylazelat, Dibutylphthalat, Dioctylphthalat, Didecylphthalat, Diphenylphthalat, Dicresylphthalat, Di-cyclohexylphthalat, Dibenzylsebacat, Triphenylphosphat, Tricresylphosphat und Trioctylphosphat. Diese organischen Mittel können nämlich verwendet werden, um den herbiziden Wirkstoff in wässrige Lösung zu bringen. e.g. lower alcohols such as methyl alcohol, ethyl alcohol or ethoxyethanol and methoxyethanol, isopropyl alcohol, ketones such as acetone, methyl ethyl ketone and cyclohexa-non, aromatic hydrocarbons such as tetrahydronaphthalene, aliphatic hydrocarbons such as kerosene, chlorinated hydrocarbons such as dichloromethane, trichloromethane, trichloromethane, trichloromethane, oxygen-containing heterocyclic compounds such as dioxane, aliphatic carboxamides such as dimethylformamide and dimethylacetamide and esters which are formed from alkanoic acids and alkanols, these having a total of between 3 and 15 carbon atoms, such as methyl acetate, butyl acetate, amyl acetate, ethyl propionate, ethyl butyrate, Amylbutirate, ethyl heptanoate, butyl heptanoate, heptyl haptanoate, ethyl caprylate, methyl caprate, ethyl caprate, methyl laurate, ethyl laurate, isopropyl laurate and methyl myristate, dimethyl sulfoxide, mineral oils, vegetable oils, animal oils and liquids generally polymerize resins for plasticizing are used, such as in particular chlorhexadecane, chloroctadecane, dioctyl adipate, dibutyl sebacate, dioctyl sebacate, dioctyl azelate, dibutyl phthalate, dioctyl phthalate, didecyl phthalate, diphenyl phthalate, dicresyl phthalate, di-cyclohexyl phthalate, dioctyl phosphate, dibutyl phthalate, dibutyl phthalate, dibutyl phthalate, dicctyl phosphate, This is because these organic agents can be used to bring the herbicidal active ingredient into aqueous solution.
Die Zusammensetzungen können durch einfache Mischung der Komponenten hergestellt werden oder, indem man in einem ersten Schritt die (den) herbiziden Wirkstoff(e) in den flüssigen oberflächenaktiven Stoff oder in eine organische Lösung desselben, gegebenenfalls unter leichtem Erwärmen, auflöst oder dispergiert und in einem zweiten Schritt die so erhaltene Lösung mit Wasser verdünnt. The compositions can be prepared by simply mixing the components or, in a first step, by dissolving or dispersing the herbicidal active ingredient (s) in the liquid surfactant or in an organic solution thereof, optionally with gentle heating, and in one second step, the solution thus obtained is diluted with water.
Die unkrautvertilgende Wirkung ist schon 2 bis 3 Stunden nach der Behandlung sichtbar und wird vollständig nach 1 bis 3 Wochen, nach welchen die ganze Windenpflanze abgetötet ist. The weed-killing effect is already visible 2 to 3 hours after the treatment and becomes complete after 1 to 3 weeks after which the entire winch plant has been killed.
Das erfindungsgemässe Verfahren wird im folgenden Beispiel veranschaulicht. The method according to the invention is illustrated in the following example.
Beispiel example
Es werden 1,66 Gewichtsteile 4-Chlor-2-methylphen-oxyessigsäure Dimethylaminsalz (entsprechend 1,46 Gewichtsteilen 4-Chlor-2-methylphenoxyessigsäure) sowie 0,83 Gewichtsteile 2,4-Dichlorphenoxyessigsäure Dimethylaminsalz in 2,05 Gewichtsteilen eines oberflächenaktiven Mittels, bestehend aus 0,02 Gewichtsteilen einer Mischung aus einem Ca-Salz eines Alkylarylsulfonats und einem Nonylphenol-polyäthoxyäthanol, (das bei 20 °C als 0,1 %ige Wasserlösung eine Oberflächenspannung von 35 Dyn/cm, und als 0,01 %ige Wasserlösung eine Oberflächenspannung von 40 Dyn/cm aufweist), 0,03 Gewichtsteile Isooktylphenolpoly-äthoxyäthanol mit 9 bis 10 Oxyäthyleneinheiten und 2 Gewichtsteilen eines Nonylphenolpolyäthoxyäthanols (AN-TAROX/CO 730 der Firma General Aniline and Film Corporation). Der erhaltenen Lösung werden 0,1 Gewichtsteile eines wasserlöslichen Konservierungsmittels, wie z.B. eine Mischung aus einem Arylmethanol und einem Halogenal-kylacylaminomethanol, und 95,46 Gewichtsteile Wasser zugegeben. Man erhält eine klare Lösung, welche aus einer mit einem speziellen Ventil ausgerüsteten Plastikflasche als Schaum punktartig auf die Windenblätter appliziert wird. Der Schaum haftet gut an den Windenblättern und fliesst nicht auf den Boden. Eine Wirkung ist schon 2 bis 3 Stunden nach der Behandlung sichtbar und eine totale Vernichtung der behandelten Winden findet nach 2 bis 3 Wochen statt. 1.66 parts by weight of 4-chloro-2-methylphenoxyacetic acid dimethylamine salt (corresponding to 1.46 parts by weight of 4-chloro-2-methylphenoxyacetic acid) and 0.83 part by weight of 2,4-dichlorophenoxyacetic acid dimethylamine salt in 2.05 parts by weight of a surfactant, consisting of 0.02 parts by weight of a mixture of a Ca salt of an alkylarylsulfonate and a nonylphenol polyethoxyethanol, (which at 20 ° C as a 0.1% water solution has a surface tension of 35 dynes / cm, and as a 0.01% water solution has a surface tension of 40 dynes / cm), 0.03 parts by weight of isooctylphenol poly-ethoxyethanol with 9 to 10 oxyethylene units and 2 parts by weight of a nonylphenol polyethoxyethanol (AN-TAROX / CO 730 from General Aniline and Film Corporation). The solution obtained is mixed with 0.1 part by weight of a water-soluble preservative, e.g. a mixture of an arylmethanol and a haloalkylacylaminomethanol, and 95.46 parts by weight of water were added. A clear solution is obtained, which is applied to the winch blades as a foam from a plastic bottle equipped with a special valve. The foam adheres well to the winch blades and does not flow to the floor. An effect is already visible 2 to 3 hours after the treatment and the treated winds are completely destroyed after 2 to 3 weeks.
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Claims (7)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH62379A CH637003A5 (en) | 1979-01-22 | 1979-01-22 | Method of controlling weeds |
| DE19803002053 DE3002053A1 (en) | 1979-01-22 | 1980-01-21 | WINCH FIGHTING METHOD |
| AT28580A AT367599B (en) | 1979-01-22 | 1980-01-21 | METHOD FOR COMBATING WINCHES AND FOAM THEREOF |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH62379A CH637003A5 (en) | 1979-01-22 | 1979-01-22 | Method of controlling weeds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH637003A5 true CH637003A5 (en) | 1983-07-15 |
Family
ID=4191313
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH62379A CH637003A5 (en) | 1979-01-22 | 1979-01-22 | Method of controlling weeds |
Country Status (3)
| Country | Link |
|---|---|
| AT (1) | AT367599B (en) |
| CH (1) | CH637003A5 (en) |
| DE (1) | DE3002053A1 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY110565A (en) * | 1990-11-28 | 1998-08-29 | Fumakilla Ltd | Foam-forming herbicidal composition and method of application |
| US5308827A (en) * | 1990-11-28 | 1994-05-03 | Fumakilla Limited | Herbicidal foam composition |
| JPH05904A (en) * | 1990-11-28 | 1993-01-08 | Fumakilla Ltd | Foam herbicidal preparation and its application method |
| WO2008068214A2 (en) | 2006-12-06 | 2008-06-12 | Akzo Nobel N.V. | Alkylamidopropyl dialkylamine surfactants as adjuvants |
| CN104814011B (en) * | 2006-12-06 | 2017-04-12 | 阿克佐诺贝尔股份有限公司 | Compatibilizer for herbicidal formulations containing 2,4‑(dichlorophenoxy) acetate |
-
1979
- 1979-01-22 CH CH62379A patent/CH637003A5/en not_active IP Right Cessation
-
1980
- 1980-01-21 AT AT28580A patent/AT367599B/en not_active IP Right Cessation
- 1980-01-21 DE DE19803002053 patent/DE3002053A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| AT367599B (en) | 1982-07-12 |
| DE3002053A1 (en) | 1980-08-07 |
| ATA28580A (en) | 1981-12-15 |
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| PL | Patent ceased | ||
| PL | Patent ceased |