CN104996417A - 用自乳化酯控制农药喷雾漂移的方法 - Google Patents
用自乳化酯控制农药喷雾漂移的方法 Download PDFInfo
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- CN104996417A CN104996417A CN201510397552.5A CN201510397552A CN104996417A CN 104996417 A CN104996417 A CN 104996417A CN 201510397552 A CN201510397552 A CN 201510397552A CN 104996417 A CN104996417 A CN 104996417A
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- GOENIMGKWNZVDA-OAMCMWGQSA-N Spinetoram Chemical compound CO[C@@H]1[C@H](OCC)[C@@H](OC)[C@H](C)O[C@H]1OC1C[C@H]2[C@@H]3C=C4C(=O)[C@H](C)[C@@H](O[C@@H]5O[C@H](C)[C@H](CC5)N(C)C)CCC[C@H](CC)OC(=O)CC4[C@@H]3CC[C@@H]2C1 GOENIMGKWNZVDA-OAMCMWGQSA-N 0.000 description 1
- 239000005930 Spinosad Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 208000006011 Stroke Diseases 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 239000005937 Tebufenozide Substances 0.000 description 1
- HBPDKDSFLXWOAE-UHFFFAOYSA-N Tebuthiuron Chemical compound CNC(=O)N(C)C1=NN=C(C(C)(C)C)S1 HBPDKDSFLXWOAE-UHFFFAOYSA-N 0.000 description 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
- SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical class CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 1
- OYVABZRZDZPVQD-UHFFFAOYSA-N [F].C=1C=CSC=1 Chemical compound [F].C=1C=CSC=1 OYVABZRZDZPVQD-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- NIXXQNOQHKNPEJ-UHFFFAOYSA-N aminopyralid Chemical compound NC1=CC(Cl)=NC(C(O)=O)=C1Cl NIXXQNOQHKNPEJ-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- GCTOSMYFALESJI-UHFFFAOYSA-N azane;2-methylpropan-2-ol Chemical compound N.CC(C)(C)O GCTOSMYFALESJI-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000000853 biopesticidal effect Effects 0.000 description 1
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- VAIZTNZGPYBOGF-UHFFFAOYSA-N butyl 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoate Chemical group C1=CC(OC(C)C(=O)OCCCC)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 VAIZTNZGPYBOGF-UHFFFAOYSA-N 0.000 description 1
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 description 1
- 229960002483 decamethrin Drugs 0.000 description 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- CNKHSLKYRMDDNQ-UHFFFAOYSA-N halofenozide Chemical compound C=1C=CC=CC=1C(=O)N(C(C)(C)C)NC(=O)C1=CC=C(Cl)C=C1 CNKHSLKYRMDDNQ-UHFFFAOYSA-N 0.000 description 1
- PMHURSZHKKJGBM-UHFFFAOYSA-N isoxaben Chemical compound O1N=C(C(C)(CC)CC)C=C1NC(=O)C1=C(OC)C=CC=C1OC PMHURSZHKKJGBM-UHFFFAOYSA-N 0.000 description 1
- YECIFGHRMFEPJK-UHFFFAOYSA-N lidocaine hydrochloride monohydrate Chemical compound O.[Cl-].CC[NH+](CC)CC(=O)NC1=C(C)C=CC=C1C YECIFGHRMFEPJK-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000013178 mathematical model Methods 0.000 description 1
- QCAWEPFNJXQPAN-UHFFFAOYSA-N methoxyfenozide Chemical compound COC1=CC=CC(C(=O)NN(C(=O)C=2C=C(C)C=C(C)C=2)C(C)(C)C)=C1C QCAWEPFNJXQPAN-UHFFFAOYSA-N 0.000 description 1
- QYPPRTNMGCREIM-UHFFFAOYSA-M methylarsonate(1-) Chemical compound C[As](O)([O-])=O QYPPRTNMGCREIM-UHFFFAOYSA-M 0.000 description 1
- FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical class CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- WRPIRSINYZBGPK-UHFFFAOYSA-N quinoxyfen Chemical compound C1=CC(F)=CC=C1OC1=CC=NC2=CC(Cl)=CC(Cl)=C12 WRPIRSINYZBGPK-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- ZNOZEKFDBJRBMI-UHFFFAOYSA-M sodium;4-(2-ethylhexoxy)-4-oxo-3-sulfobutanoate Chemical compound [Na+].CCCCC(CC)COC(=O)C(S(O)(=O)=O)CC([O-])=O ZNOZEKFDBJRBMI-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000013599 spices Nutrition 0.000 description 1
- 229940014213 spinosad Drugs 0.000 description 1
- 229930185156 spinosyn Natural products 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- WOSNCVAPUOFXEH-UHFFFAOYSA-N thifluzamide Chemical compound S1C(C)=NC(C(F)(F)F)=C1C(=O)NC1=C(Br)C=C(OC(F)(F)F)C=C1Br WOSNCVAPUOFXEH-UHFFFAOYSA-N 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 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
- 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
- A01N25/24—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 containing ingredients to enhance the sticking of the active ingredients
-
- 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
- A01N25/30—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 characterised by the surfactants
-
- 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
-
- 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
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Catching Or Destruction (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11006008P | 2008-10-31 | 2008-10-31 | |
| US61/110,060 | 2008-10-31 | ||
| CN2009801416581A CN102186340A (zh) | 2008-10-31 | 2009-10-30 | 用自乳化酯控制农药喷雾漂移的方法 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2009801416581A Division CN102186340A (zh) | 2008-10-31 | 2009-10-30 | 用自乳化酯控制农药喷雾漂移的方法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN104996417A true CN104996417A (zh) | 2015-10-28 |
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Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201510397552.5A Pending CN104996417A (zh) | 2008-10-31 | 2009-10-30 | 用自乳化酯控制农药喷雾漂移的方法 |
| CN2009801416581A Pending CN102186340A (zh) | 2008-10-31 | 2009-10-30 | 用自乳化酯控制农药喷雾漂移的方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2009801416581A Pending CN102186340A (zh) | 2008-10-31 | 2009-10-30 | 用自乳化酯控制农药喷雾漂移的方法 |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US20100113275A1 (https=) |
| EP (1) | EP2348836B1 (https=) |
| JP (2) | JP5653926B2 (https=) |
| CN (2) | CN104996417A (https=) |
| AR (1) | AR075294A1 (https=) |
| AU (1) | AU2009308821B2 (https=) |
| BR (1) | BRPI0920002B8 (https=) |
| CA (1) | CA2739700C (https=) |
| CO (1) | CO6361858A2 (https=) |
| MX (1) | MX2011004586A (https=) |
| WO (1) | WO2010051435A2 (https=) |
| ZA (1) | ZA201101895B (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109310080A (zh) * | 2016-07-01 | 2019-02-05 | 禾大公司 | 喷雾漂移减少 |
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| JPS6093592A (ja) * | 1983-10-26 | 1985-05-25 | シャープ株式会社 | 家屋内警備システム |
| ES2493928T3 (es) * | 2010-06-08 | 2014-09-12 | Dow Agrosciences Llc | Aceites microencapsulados para el control de propagación de pulverización de plaguicidas |
| ES2767282T3 (es) * | 2010-09-15 | 2020-06-17 | Dow Agrosciences Llc | Tensioactivos de amina para controlar la deriva de pulverización de herbicidas |
| US20130150241A1 (en) | 2011-04-20 | 2013-06-13 | Huntsman Petrochemical Llc | Spray drift reduction agents comprising low hydrophilic-lipophilic balance surfactants |
| WO2012150162A1 (en) * | 2011-05-02 | 2012-11-08 | Basf Se | A method for enhancing the performance of a pesticide with guanidines |
| WO2013040006A1 (en) | 2011-09-12 | 2013-03-21 | Rhodia Operations | Agricultural pesticide compositions |
| CN104244719B (zh) * | 2012-03-23 | 2016-10-12 | 陶氏益农公司 | 包含脂肪酸烷基酯、脂肪酸酰胺、或甘油三脂肪酸酯的含水除草浓缩物及使用方法 |
| PT2833715T (pt) * | 2012-04-02 | 2019-06-05 | Dow Agrosciences Llc | Ésteres aromáticos para controlar a deriva em pulverizações agrícolas |
| JP6729925B2 (ja) | 2012-05-30 | 2020-07-29 | クラリアント・ファイナンス・(ビーブイアイ)・リミテッド | N−メチル−n−アシルグルカミン含有組成物 |
| WO2013178671A2 (de) | 2012-05-30 | 2013-12-05 | Clariant International Ltd. | Verwendung von n-methyl-n-acylglucaminen als solubilisatoren |
| CA2873822C (en) * | 2012-06-21 | 2020-09-22 | Basf Se | An aqueous composition comprising dicamba, and a fatty alcohol alkoxylate as a drift control agent |
| CN105025710A (zh) * | 2012-10-23 | 2015-11-04 | 罗地亚经营管理公司 | 农药组合物 |
| WO2014063818A1 (de) * | 2012-10-24 | 2014-05-01 | Clariant International Ltd | Driftreduzierende zusammensetzungen |
| DE102012021647A1 (de) | 2012-11-03 | 2014-05-08 | Clariant International Ltd. | Wässrige Adjuvant-Zusammensetzungen |
| EP3032950B1 (en) | 2013-08-14 | 2023-05-31 | Croda, Inc. | Spray drift reduction |
| RU2631235C2 (ru) | 2013-08-14 | 2017-09-20 | Крода, Инк. | Комбинация вспомогательных веществ |
| UY35923A (es) * | 2013-12-30 | 2015-07-31 | Rhodia Operations | ?composiciones pesticidas agrícolas?. |
| BR112016022386A2 (pt) | 2014-03-28 | 2018-06-19 | Schertz Aerial Service Inc | sistema e método de pulverização |
| DE102014005771A1 (de) * | 2014-04-23 | 2015-10-29 | Clariant International Ltd. | Verwendung von wässrigen driftreduzierenden Zusammensetzungen |
| DE102014211826A1 (de) | 2014-06-20 | 2015-12-24 | Evonik Degussa Gmbh | Verwendung von Entschäumern als Anti-Drift-Additive |
| BR112017002519A2 (pt) * | 2014-08-15 | 2017-12-05 | Clariant Int Ltd | uso de ésteres de lactato eterificados para redução do desvio durante a aplicação de agentes de tratamento de plantas |
| EP3203838B1 (de) * | 2014-10-08 | 2020-04-01 | Evonik Operations GmbH | Verwendung von hydrophoben, selbstemulgierenden polyglycerinestern als adjuvantien und anti-spray-drift mittel |
| WO2016087473A1 (de) * | 2014-12-01 | 2016-06-09 | Clariant International Ltd | Verwendung von tributylphenolalkoxylaten zur verminderung der drift bei der applikation von pflanzenbehandlungsmitteln |
| BR112017011737A2 (pt) * | 2014-12-05 | 2017-12-26 | Clariant Int Ltd | uso de derivados de óleos vegetais alcoxilados para reduzir o desvio na aplicação de agentes de tratamento de plantas |
| AU2016235791A1 (en) * | 2015-03-25 | 2017-09-21 | Huntsman Petrochemical Llc | Maleated natural oil derivatives as agrochemical inert ingredients |
| US20160374334A1 (en) | 2015-06-29 | 2016-12-29 | Lamberti Spa | Method for reducing spray drift |
| CA2992119C (en) | 2015-07-14 | 2023-08-29 | Rhodia Operations | Agricultural adjuvant compositions of oil/surfactant/salt emulsions and methods for use |
| DE102015219651A1 (de) | 2015-10-09 | 2017-04-13 | Clariant International Ltd. | Zusammensetzungen enthaltend Zuckeramin und Fettsäure |
| DE202015008045U1 (de) | 2015-10-09 | 2015-12-09 | Clariant International Ltd. | Universelle Pigmentdispersionen auf Basis von N-Alkylglukaminen |
| DE202016003070U1 (de) | 2016-05-09 | 2016-06-07 | Clariant International Ltd. | Stabilisatoren für Silikatfarben |
| US12133526B1 (en) | 2016-08-19 | 2024-11-05 | Ethox Chemicals, LLC. | Drift control additive |
| CN109090108B (zh) * | 2018-09-13 | 2021-03-02 | 江苏擎宇化工科技有限公司 | 一种乳化植物油乳化剂组合物及其制备方法 |
| CN109287632A (zh) * | 2018-09-26 | 2019-02-01 | 广西田园生化股份有限公司 | 一种油基农药制剂增效剂组合物及其应用 |
| US20200236925A1 (en) * | 2019-01-24 | 2020-07-30 | Bayer Cropscience Lp | Methods and formulations for preventing downward migration of agricultural materials |
| UY39010A (es) | 2020-01-10 | 2021-08-31 | Monsanto Technology Llc | Composiciones de herbicidas de auxina que incluyen agentes retardantes de la deriva y métodos de preparacion de las mismas |
| UY39009A (es) | 2020-01-10 | 2021-08-31 | Monsanto Technology Llc | Composiciones herbicidas que incluyen agentes retardantes de la deriva y métodos de preparación de las mismas |
| CN114621803B (zh) * | 2020-12-10 | 2023-06-30 | 中国石油天然气股份有限公司 | 一种自乳化酯及其制备方法 |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5543035A (en) * | 1978-09-21 | 1980-03-26 | Toho Chem Ind Co Ltd | Low drifting powdery pesticide |
| JPH0912407A (ja) * | 1995-06-26 | 1997-01-14 | Hokko Chem Ind Co Ltd | ドリフト防止剤および改良された農薬粉剤 |
| US6103770A (en) * | 1995-01-18 | 2000-08-15 | Societe D'exploitation De Pruduits Pour Les Industries Chimiques - Seppic | Utilization of ethoxylated fatty acid esters as self-emulsifiable compounds |
| US6797673B1 (en) * | 2002-05-01 | 2004-09-28 | Platte Chemical Company | Lecithin-containing drift reduction composition for use in spraying agricultural acreage |
| CN1553768A (zh) * | 2001-09-06 | 2004-12-08 | 新的化合物 | |
| WO2007081961A2 (en) * | 2006-01-10 | 2007-07-19 | Innovaform Technologies, Llc | Pesticide delivery system |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3912642A (en) * | 1973-08-01 | 1975-10-14 | Emery Industries Inc | Ester lubricants suitable for use in aqueous systems |
| US4559226A (en) * | 1983-09-06 | 1985-12-17 | Bernel Chemical Company Inc. | Self-emulsifying alkoxylate esters |
| DK653488D0 (da) | 1988-11-23 | 1988-11-23 | Esti Kemi Aps | Smoeremiddel |
| JP3512414B2 (ja) * | 1993-06-02 | 2004-03-29 | ユニケマ・ケミー・ベー・ヴェー | 基剤流体 |
| WO1995007961A1 (en) * | 1993-09-14 | 1995-03-23 | Unichema Chemie B.V. | Base fluids |
| GB2306965B (en) * | 1995-11-06 | 1999-09-01 | American Cyanamid Co | Aqueous spray compositions |
| US6060438A (en) * | 1998-10-27 | 2000-05-09 | D. A. Stuart | Emulsion for the hot rolling of non-ferrous metals |
| US6566308B1 (en) * | 1999-01-29 | 2003-05-20 | Basf Aktiengesellschaft | Emulsifiable concentrate containing one or more pesticides and adjuvants |
| JP2002114601A (ja) * | 2000-10-06 | 2002-04-16 | Sumitomo Chem Co Ltd | 殺虫エアゾール用組成物 |
| EA012031B1 (ru) * | 2002-12-13 | 2009-06-30 | Байер Кропсайенс Аг | Гербицидный масляный суспензионный концентрат, способ его получения, применения и способ борьбы с сорными растениями |
| JP4480962B2 (ja) * | 2003-06-30 | 2010-06-16 | アース製薬株式会社 | 殺虫組成物の殺虫効力の残効性向上方法 |
| US20090209441A1 (en) | 2004-01-09 | 2009-08-20 | The Lubrizol Corporation | Maleated vegetable oils and derivatives, as self-emulsifying lubricants in metalworking |
| US8153145B2 (en) * | 2005-12-22 | 2012-04-10 | Fmc Corporation | Formulations of bifenthrin and enriched cypermethrin |
| WO2008079304A2 (en) | 2006-12-21 | 2008-07-03 | Croda Uniqema, Inc. | Composition and method |
| GB0703394D0 (en) | 2007-02-22 | 2007-03-28 | Ciba Sc Holding Ag | Process for Preparing and Applying Pesticide or Herbicide Formulation |
| TW200843642A (en) * | 2007-03-08 | 2008-11-16 | Du Pont | Liquid sulfonylurea herbicide formulations |
-
2009
- 2009-10-29 AR ARP090104172A patent/AR075294A1/es active IP Right Grant
- 2009-10-30 CN CN201510397552.5A patent/CN104996417A/zh active Pending
- 2009-10-30 EP EP09744579.5A patent/EP2348836B1/en active Active
- 2009-10-30 AU AU2009308821A patent/AU2009308821B2/en active Active
- 2009-10-30 JP JP2011534804A patent/JP5653926B2/ja active Active
- 2009-10-30 CN CN2009801416581A patent/CN102186340A/zh active Pending
- 2009-10-30 MX MX2011004586A patent/MX2011004586A/es unknown
- 2009-10-30 US US12/609,404 patent/US20100113275A1/en not_active Abandoned
- 2009-10-30 CA CA2739700A patent/CA2739700C/en active Active
- 2009-10-30 BR BRPI0920002A patent/BRPI0920002B8/pt active IP Right Grant
- 2009-10-30 WO PCT/US2009/062734 patent/WO2010051435A2/en not_active Ceased
-
2011
- 2011-03-11 ZA ZA2011/01895A patent/ZA201101895B/en unknown
- 2011-04-14 CO CO11046642A patent/CO6361858A2/es active IP Right Grant
-
2014
- 2014-07-29 JP JP2014153686A patent/JP5728114B2/ja active Active
-
2016
- 2016-06-09 US US15/177,410 patent/US11172679B2/en active Active
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5543035A (en) * | 1978-09-21 | 1980-03-26 | Toho Chem Ind Co Ltd | Low drifting powdery pesticide |
| US6103770A (en) * | 1995-01-18 | 2000-08-15 | Societe D'exploitation De Pruduits Pour Les Industries Chimiques - Seppic | Utilization of ethoxylated fatty acid esters as self-emulsifiable compounds |
| JPH0912407A (ja) * | 1995-06-26 | 1997-01-14 | Hokko Chem Ind Co Ltd | ドリフト防止剤および改良された農薬粉剤 |
| CN1553768A (zh) * | 2001-09-06 | 2004-12-08 | 新的化合物 | |
| US6797673B1 (en) * | 2002-05-01 | 2004-09-28 | Platte Chemical Company | Lecithin-containing drift reduction composition for use in spraying agricultural acreage |
| WO2007081961A2 (en) * | 2006-01-10 | 2007-07-19 | Innovaform Technologies, Llc | Pesticide delivery system |
Non-Patent Citations (2)
| Title |
|---|
| C. STAINIER ET AL.: "Droplet size spectra and drift effect of two phenmedipham formulations and four adjuvants mixtures", 《CROP PRODUCTION》 * |
| M. A. APODACA ET AL.: "DRIFT CONTROL POLYMERS AND FORMULATION TYPE AFFECT VOLUMETRIC DROPLET SIZE SPECTRA OF PROPANIL SPRAYS", 《JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH, PART B》 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109310080A (zh) * | 2016-07-01 | 2019-02-05 | 禾大公司 | 喷雾漂移减少 |
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| MX2011004586A (es) | 2011-06-17 |
| CA2739700A1 (en) | 2010-05-06 |
| AR075294A1 (es) | 2011-03-23 |
| US20100113275A1 (en) | 2010-05-06 |
| JP2012507561A (ja) | 2012-03-29 |
| ZA201101895B (en) | 2012-05-30 |
| JP5728114B2 (ja) | 2015-06-03 |
| CO6361858A2 (es) | 2012-01-20 |
| BRPI0920002A2 (pt) | 2019-11-19 |
| CN102186340A (zh) | 2011-09-14 |
| CA2739700C (en) | 2017-09-05 |
| EP2348836A2 (en) | 2011-08-03 |
| WO2010051435A3 (en) | 2011-04-21 |
| BRPI0920002B8 (pt) | 2022-10-11 |
| AU2009308821B2 (en) | 2015-01-29 |
| US11172679B2 (en) | 2021-11-16 |
| BRPI0920002B1 (pt) | 2020-12-29 |
| AU2009308821A1 (en) | 2010-05-06 |
| EP2348836B1 (en) | 2017-01-11 |
| JP2014240403A (ja) | 2014-12-25 |
| JP5653926B2 (ja) | 2015-01-14 |
| WO2010051435A2 (en) | 2010-05-06 |
| US20160278370A1 (en) | 2016-09-29 |
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