DD209952A5 - Verfahren zum ausbringen von pflanzenschutzmittelspritzbruehen - Google Patents

Verfahren zum ausbringen von pflanzenschutzmittelspritzbruehen Download PDF

Info

Publication number: DD209952A5
Authority: DD; German Democratic Republic
Prior art keywords: phospholipid; spray; concentrate; concentrates; active ingredient
Prior art date: 1982-07-09

Application number

DD83252807A

Other languages

German (de)

English (en)

Inventor

Miklos Ghyczy

Paul-Robert Imberge

Armin Wendel

Original Assignee

Nattermann A & Cie

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1982-07-09

Filing date

1983-07-06

Publication date

1984-05-30

1983-07-06 Application filed by Nattermann A & Cie filed Critical Nattermann A & Cie

1984-05-30 Publication of DD209952A5 publication Critical patent/DD209952A5/de

Links

238000000034 method Methods 0.000 title claims abstract description 23
230000008569 process Effects 0.000 title abstract description 8
239000007921 spray Substances 0.000 claims abstract description 68
150000003904 phospholipids Chemical class 0.000 claims abstract description 63
239000000203 mixture Substances 0.000 claims abstract description 58
239000012141 concentrate Substances 0.000 claims abstract description 57
239000004480 active ingredient Substances 0.000 claims abstract description 29
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 26
239000013543 active substance Substances 0.000 claims description 23
238000002156 mixing Methods 0.000 claims description 15
238000004806 packaging method and process Methods 0.000 claims description 14
239000000575 pesticide Substances 0.000 claims description 10
239000007788 liquid Substances 0.000 claims description 8
WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 claims description 8
238000002360 preparation method Methods 0.000 claims description 7
JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 claims description 6
150000008104 phosphatidylethanolamines Chemical class 0.000 claims description 6
238000010790 dilution Methods 0.000 claims description 4
239000012895 dilution Substances 0.000 claims description 4
150000008105 phosphatidylcholines Chemical class 0.000 claims description 4
238000007865 diluting Methods 0.000 claims description 3
230000007480 spreading Effects 0.000 claims description 3
TZCPCKNHXULUIY-RGULYWFUSA-N 1,2-distearoyl-sn-glycero-3-phosphoserine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC TZCPCKNHXULUIY-RGULYWFUSA-N 0.000 claims description 2
ZWZWYGMENQVNFU-UHFFFAOYSA-N Glycerophosphorylserin Natural products OC(=O)C(N)COP(O)(=O)OCC(O)CO ZWZWYGMENQVNFU-UHFFFAOYSA-N 0.000 claims description 2
ATBOMIWRCZXYSZ-XZBBILGWSA-N [1-[2,3-dihydroxypropoxy(hydroxy)phosphoryl]oxy-3-hexadecanoyloxypropan-2-yl] (9e,12e)-octadeca-9,12-dienoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(COP(O)(=O)OCC(O)CO)OC(=O)CCCCCCC\C=C\C\C=C\CCCCC ATBOMIWRCZXYSZ-XZBBILGWSA-N 0.000 claims description 2
AWUCVROLDVIAJX-UHFFFAOYSA-N alpha-glycerophosphate Natural products OCC(O)COP(O)(O)=O AWUCVROLDVIAJX-UHFFFAOYSA-N 0.000 claims description 2
239000008350 hydrogenated phosphatidyl choline Substances 0.000 claims description 2
150000003905 phosphatidylinositols Chemical class 0.000 claims description 2
ASWBNKHCZGQVJV-UHFFFAOYSA-N (3-hexadecanoyloxy-2-hydroxypropyl) 2-(trimethylazaniumyl)ethyl phosphate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)COP([O-])(=O)OCC[N+](C)(C)C ASWBNKHCZGQVJV-UHFFFAOYSA-N 0.000 claims 1
239000004615 ingredient Substances 0.000 abstract 1
238000012856 packing Methods 0.000 abstract 1
235000008504 concentrate Nutrition 0.000 description 39
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 28
239000000839 emulsion Substances 0.000 description 22
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 14
241000196324 Embryophyta Species 0.000 description 10
235000011187 glycerol Nutrition 0.000 description 10
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
239000000243 solution Substances 0.000 description 9
239000002904 solvent Substances 0.000 description 9
239000004563 wettable powder Substances 0.000 description 8
238000009472 formulation Methods 0.000 description 7
239000000725 suspension Substances 0.000 description 7
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
239000000843 powder Substances 0.000 description 6
230000000694 effects Effects 0.000 description 5
239000004009 herbicide Substances 0.000 description 5
239000002917 insecticide Substances 0.000 description 5
239000003921 oil Substances 0.000 description 5
229920006395 saturated elastomer Polymers 0.000 description 5
IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
239000007957 coemulsifier Substances 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
238000007599 discharging Methods 0.000 description 4
229940079593 drug Drugs 0.000 description 4
239000003814 drug Substances 0.000 description 4
239000003995 emulsifying agent Substances 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
230000002363 herbicidal effect Effects 0.000 description 4
239000000787 lecithin Substances 0.000 description 4
235000010445 lecithin Nutrition 0.000 description 4
229940067606 lecithin Drugs 0.000 description 4
235000019198 oils Nutrition 0.000 description 4
-1 phospholipid citrate Chemical class 0.000 description 4
239000004476 plant protection product Substances 0.000 description 4
239000000047 product Substances 0.000 description 4
239000011734 sodium Substances 0.000 description 4
238000005507 spraying Methods 0.000 description 4
239000000126 substance Substances 0.000 description 4
WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 description 3
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
238000001704 evaporation Methods 0.000 description 3
230000008020 evaporation Effects 0.000 description 3
150000004665 fatty acids Chemical class 0.000 description 3
239000000499 gel Substances 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
239000002689 soil Substances 0.000 description 3
238000003756 stirring Methods 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
239000005562 Glyphosate Substances 0.000 description 2
239000005949 Malathion Substances 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
241000607479 Yersinia pestis Species 0.000 description 2
230000000895 acaricidal effect Effects 0.000 description 2
230000008901 benefit Effects 0.000 description 2
JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 2
229940097068 glyphosate Drugs 0.000 description 2
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
230000000749 insecticidal effect Effects 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
229960000453 malathion Drugs 0.000 description 2
239000002480 mineral oil Substances 0.000 description 2
235000010446 mineral oil Nutrition 0.000 description 2
239000005645 nematicide Substances 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
239000003791 organic solvent mixture Substances 0.000 description 2
235000020354 squash Nutrition 0.000 description 2
230000003068 static effect Effects 0.000 description 2
235000015112 vegetable and seed oil Nutrition 0.000 description 2
239000008158 vegetable oil Substances 0.000 description 2
235000013311 vegetables Nutrition 0.000 description 2
239000007762 w/o emulsion Substances 0.000 description 2
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
LEEANUDEDHYDTG-UHFFFAOYSA-N 1,2-dimethoxypropane Chemical compound COCC(C)OC LEEANUDEDHYDTG-UHFFFAOYSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
JOLQKTGDSGKSKJ-UHFFFAOYSA-N 1-ethoxypropan-2-ol Chemical compound CCOCC(C)O JOLQKTGDSGKSKJ-UHFFFAOYSA-N 0.000 description 1
DJMUYABFXCIYSC-UHFFFAOYSA-N 1H-phosphole Chemical compound C=1C=CPC=1 DJMUYABFXCIYSC-UHFFFAOYSA-N 0.000 description 1
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical class NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
PWVXXGRKLHYWKM-UHFFFAOYSA-N 5-[2-(benzenesulfonyl)ethyl]-3-[(1-methylpyrrolidin-2-yl)methyl]-1h-indole Chemical compound CN1CCCC1CC(C1=C2)=CNC1=CC=C2CCS(=O)(=O)C1=CC=CC=C1 PWVXXGRKLHYWKM-UHFFFAOYSA-N 0.000 description 1
239000005493 Chloridazon (aka pyrazone) Substances 0.000 description 1
239000005752 Copper oxychloride Substances 0.000 description 1
239000005946 Cypermethrin Substances 0.000 description 1
RDJTWDKSYLLHRW-UHFFFAOYSA-N Dinoseb acetate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(C)=O RDJTWDKSYLLHRW-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical class CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
239000005621 Terbuthylazine Substances 0.000 description 1
GBAWQJNHVWMTLU-RQJHMYQMSA-N [(1R,5S)-7-chloro-6-bicyclo[3.2.0]hepta-2,6-dienyl] dimethyl phosphate Chemical compound C1=CC[C@@H]2C(OP(=O)(OC)OC)=C(Cl)[C@@H]21 GBAWQJNHVWMTLU-RQJHMYQMSA-N 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000009471 action Effects 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
230000006978 adaptation Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
239000003905 agrochemical Substances 0.000 description 1
239000003513 alkali Substances 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
230000008859 change Effects 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
WYKYKTKDBLFHCY-UHFFFAOYSA-N chloridazon Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1 WYKYKTKDBLFHCY-UHFFFAOYSA-N 0.000 description 1
HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 description 1
239000013065 commercial product Substances 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
229960005424 cypermethrin Drugs 0.000 description 1
KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 description 1
238000013461 design Methods 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000005538 encapsulation Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
125000005456 glyceride group Chemical group 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 description 1
150000002632 lipids Chemical class 0.000 description 1
239000002502 liposome Substances 0.000 description 1
244000144972 livestock Species 0.000 description 1
150000004668 long chain fatty acids Chemical class 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 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
239000012071 phase Substances 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920000136 polysorbate Polymers 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
239000002243 precursor Substances 0.000 description 1
QXJKBPAVAHBARF-BETUJISGSA-N procymidone Chemical compound O=C([C@]1(C)C[C@@]1(C1=O)C)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-BETUJISGSA-N 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
IKVXBIIHQGXQRQ-UHFFFAOYSA-N propan-2-yl 2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N(C(C)C(=O)OC(C)C)C(=O)C1=CC=CC=C1 IKVXBIIHQGXQRQ-UHFFFAOYSA-N 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
235000013772 propylene glycol Nutrition 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000009467 reduction Effects 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
238000010008 shearing Methods 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
RNVYQYLELCKWAN-UHFFFAOYSA-N solketal Chemical compound CC1(C)OCC(CO)O1 RNVYQYLELCKWAN-UHFFFAOYSA-N 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
235000000346 sugar Nutrition 0.000 description 1
150000008163 sugars Chemical class 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000004546 suspension concentrate Substances 0.000 description 1
FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
238000012546 transfer Methods 0.000 description 1
238000011282 treatment Methods 0.000 description 1
ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
238000009736 wetting Methods 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
- A01N25/02—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 liquids as carriers, diluents or solvents
- 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
- A01N25/02—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 liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Dentistry (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Toxicology (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
Wood Science & Technology (AREA)
Pest Control & Pesticides (AREA)
Environmental Sciences (AREA)
Chemical & Material Sciences (AREA)
Dispersion Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
Fertilizers (AREA)
Catching Or Destruction (AREA)

DD83252807A 1982-07-09 1983-07-06 Verfahren zum ausbringen von pflanzenschutzmittelspritzbruehen DD209952A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19823225705 DE3225705A1 (de)	1982-07-09	1982-07-09	Verfahren zum ausbringen von pflanzenschutzmittelspritzbruehen durch verspruehen und verpackungseinheit fuer konzentrate

Publications (1)

Publication Number	Publication Date
DD209952A5 true DD209952A5 (de)	1984-05-30

Family

ID=6168029

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD83252807A DD209952A5 (de)	1982-07-09	1983-07-06	Verfahren zum ausbringen von pflanzenschutzmittelspritzbruehen

Country Status (12)

Country	Link
US (1)	US4506831A (pt)
EP (1)	EP0099039B1 (pt)
JP (1)	JPS5921605A (pt)
AT (1)	ATE24263T1 (pt)
AU (1)	AU1669883A (pt)
BR (1)	BR8303676A (pt)
CA (1)	CA1203992A (pt)
DD (1)	DD209952A5 (pt)
DE (2)	DE3225705A1 (pt)
HU (1)	HU188993B (pt)
PL (1)	PL242927A1 (pt)
ZA (1)	ZA834999B (pt)

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US4610311A (en) *	1983-02-15	1986-09-09	Sanitek Products, Inc.	Method for reducing the aerial drift of aqueous preparations
US4863899A (en) *	1983-05-09	1989-09-05	Todaro George J	Biologically active polypeptides
YU45662B (sh) *	1983-09-20	1992-07-20	Berol Nobel (Suisse) S.A.	Postupak za dobijanje fenmedifama ili dezmedifama
CZ156191A3 (en) *	1984-02-29	1995-10-18	Schering Ag	Stabilized liquid herbicidal agent and method of controlling weed
US5246912A (en) *	1984-02-29	1993-09-21	Berol Nobel (Suisse) S.A.	Herbicidal compositions of phenmedipham and desmedipham
JPS6157506A (ja) *	1984-08-29	1986-03-24	Sanyo Mokuzai Boufu Kk	防虫防蟻組成物
EP0379851A1 (en) *	1988-12-27	1990-08-01	Monsanto Company	Dispensable pesticide-containing compositions
JPH05137970A (ja) *	1991-11-19	1993-06-01	Mitsui Eng & Shipbuild Co Ltd	アルコールの回収方法
FR2713235B1 (fr) *	1993-11-29	1996-01-19	Rhone Poulenc Agrochimie	Composition pour aérosol et système générateur d'aérosol la contenant.
US5821195A (en) *	1996-08-16	1998-10-13	Monsanto Company	Sequential application method for enhancing glyphosate herbicidal effectiveness with reduced antagonism
ATE252827T1 (de) *	1996-08-16	2003-11-15	Monsanto Technology Llc	Reihenanordnungsmethode zur behandlung von pflanzen mit exogenen chemikalien
US6130186A (en) *	1996-10-25	2000-10-10	Monsanto Company	Composition and method for treating plants with exogenous chemicals
CZ299552B6 (cs) *	1996-10-25	2008-09-03	Monsanto Technology Llc	Kompozice a zpusob pro ošetrení rostlin exogenními chemikáliemi
US7046682B2 (en) *	1997-02-12	2006-05-16	Elster Electricity, Llc.	Network-enabled, extensible metering system
US5906316A (en) *	1997-09-04	1999-05-25	S. C. Johnson & Son, Inc.	Nozzle to dispense active material
WO2002044305A2 (en) *	2000-11-28	2002-06-06	Astaris Llc	Fire retardant compositions with reduced aluminum corrosivity
US6743756B2 (en) *	2001-01-26	2004-06-01	Benchmark Research And Technology, Inc.	Suspensions of particles in non-aqueous solvents
US7037535B2 (en) *	2002-11-19	2006-05-02	Kimberly-Clark Worldwide, Inc.	Method and composition for neutralizing house dust mite feces
US20060233863A1 (en)	2003-02-10	2006-10-19	Enzymotec Ltd.	Oils enriched with diacylglycerols and phytosterol esters and unit dosage forms thereof for use in therapy
AU2005270831B2 (en)	2004-08-10	2011-08-25	Enzymotec Ltd.	Mixture of phytosterol ester(s) and 1, 3-diglyceride(s) for use in the treatment of medical conditions
US9416065B2 (en)	2007-02-12	2016-08-16	Archer Daniels Midland Company	Adjuvants and methods of using them
BRPI0915271A2 (pt) *	2008-11-14	2016-06-14	Archer Daniels Midland Co	composição de organo-gel fosfolipídico estruturado termorreversível, uso da composição de organo-gel fosfolipídico estruturado termorreversível, processo para a obtenção de um produto cristalino líquido e método de carregar organo-gel fosfolipídico estruturado termorreversível
US20120142533A1 (en) *	2009-06-15	2012-06-07	Accuform Technologies, Llc	Reduced vaporization compositions and methods
BR112012029040A2 (pt)	2010-05-14	2016-08-02	Archer Daniels Midland Co	composição de organogel de fosfolipideo estruturado termorreversível comestível para uso em produto alimentício, método de estruturar uma fase orgânica comestível, produto ou ingrediente alimentício, composição, método de carregar um organogel de fosfolipídeo estruturado termorreversível comestível, método de revestir um alimento e composição de organogel de fosfolipídeo estruturado termorreversivel comestível para uso em um produto alimentício
WO2012068105A2 (en)	2010-11-15	2012-05-24	Archer Daniels Midland Company	Compositions and uses thereof in converting contaminants
ES2733112T3 (es) *	2013-05-23	2019-11-27	Syngenta Participations Ag	Formulaciones de mezcla de tanque
WO2014187846A1 (en) *	2013-05-23	2014-11-27	Syngenta Participations Ag	Tank-mix formulations

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US1938864A (en) *	1929-10-21	1933-12-12	Firm Hanseatische Muhlenwerke	Insecticidal emulsion
US2006227A (en) *	1932-10-19	1935-06-25	Grasselli Chemical Co	Contact insecticide
GB944229A (en) *	1960-06-07	1963-12-11	Stull Chemical	Apparatus and process for mixing and dispensing fluids
US3052599A (en) *	1960-06-15	1962-09-04	American Cyanamid Co	Stabilized organic phosphate pesticidal compositions in fuel oil
DE2422954A1 (de) *	1974-05-11	1975-11-13	Bayer Ag	Mittel zur reduzierung der drift beim ausbringen waessriger spritzbruehen von pflanzenschutzmitteln
IE50142B1 (en) *	1979-07-11	1986-02-19	Sampson Michael James	Improved method of using a plant-growth regulator
US4238072A (en) *	1979-11-29	1980-12-09	Nicola Licursi	Method of dispensing a granular fertilizer
DE3125447A1 (de) *	1981-06-27	1983-01-13	A. Nattermann & Cie GmbH, 5000 Köln	Neue nematizid-zusammensetzung, verfahren zur herstellung und deren verwendung
DE3125423A1 (de) *	1981-06-27	1983-01-13	A. Nattermann & Cie GmbH, 5000 Köln	Neue insektizid-zusammensetzung, verfahren zur herstellung und deren verwendung
DE3125399A1 (de) *	1981-06-27	1983-01-13	A. Nattermann & Cie GmbH, 5000 Köln	Neue herbizid-zusammensetzung, verfahren zur herstellung und deren verwendung
DE3125422A1 (de) *	1981-06-27	1983-01-27	A. Nattermann & Cie GmbH, 5000 Köln	Neue fungizid-zusammensetzung, verfahren zur herstellung und deren verwendung
DE3125448A1 (de) *	1981-06-27	1983-01-13	A. Nattermann & Cie GmbH, 5000 Köln	"neue acarizid-zusammensetzung, verfahren zur herstellung und deren verwendung"

1982
- 1982-07-09 DE DE19823225705 patent/DE3225705A1/de not_active Ceased
1983
- 1983-06-28 US US06/508,663 patent/US4506831A/en not_active Expired - Fee Related
- 1983-07-02 AT AT83106465T patent/ATE24263T1/de not_active IP Right Cessation
- 1983-07-02 EP EP83106465A patent/EP0099039B1/de not_active Expired
- 1983-07-02 DE DE8383106465T patent/DE3368372D1/de not_active Expired
- 1983-07-05 JP JP58121123A patent/JPS5921605A/ja active Pending
- 1983-07-06 CA CA000431955A patent/CA1203992A/en not_active Expired
- 1983-07-06 DD DD83252807A patent/DD209952A5/de not_active IP Right Cessation
- 1983-07-08 AU AU16698/83A patent/AU1669883A/en not_active Abandoned
- 1983-07-08 HU HU832456A patent/HU188993B/hu not_active IP Right Cessation
- 1983-07-08 ZA ZA834999A patent/ZA834999B/xx unknown
- 1983-07-08 PL PL24292783A patent/PL242927A1/xx unknown
- 1983-07-08 BR BR8303676A patent/BR8303676A/pt unknown

Also Published As

Publication number	Publication date
JPS5921605A (ja)	1984-02-03
EP0099039B1 (de)	1986-12-17
CA1203992A (en)	1986-05-06
DE3225705A1 (de)	1984-01-12
US4506831A (en)	1985-03-26
EP0099039A1 (de)	1984-01-25
HU188993B (en)	1986-05-28
AU1669883A (en)	1984-01-12
BR8303676A (pt)	1984-02-14
PL242927A1 (en)	1984-07-02
DE3368372D1 (en)	1987-01-29
HUT36047A (en)	1985-08-28
ZA834999B (en)	1984-04-25
ATE24263T1 (de)	1987-01-15

Legal Events

Date	Code	Title	Description
2000-04-13	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
DD209952A5 (de)	1984-05-30	Verfahren zum ausbringen von pflanzenschutzmittelspritzbruehen
DE3225703C1 (de)	1984-01-19	Phospholipidkonzentrat und seine Verwendung als Hilfsstoff zum Herstellen und Austragen von Pflanzenschutzmittel enthaltenden Spritzbruehen
DE60117403T2 (de)	2006-11-23	Agrochemisches formulierungshilfsmittel und dessen verwendung
EP1035771B1 (de)	2004-11-03	Tensidsysteme für flüssige wässrige zubereitungen
DE3887513T2 (de)	1994-06-16	Chemische formulierungen.
EP0407874B1 (de)	1995-01-18	Entschäumer für flüssige Netzmittel und schaumarme flüssige Pflanzenschutzmittel
DD207140A5 (de)	1984-02-22	Herbizide emulsionen
EP0357559A2 (de)	1990-03-07	Wässrige Formulierungen und deren Verwendung
DE3009944C2 (de)	1994-01-20	Insektizide Öl-in-Wasser-Emulsion
DE3141224C2 (de)	1995-11-30	Behandlung von Ectoparasiten bei Schweinen
DE3700881A1 (de)	1987-07-23	Zur schaedlingsbekaempfung geeignete oel-in-wasser-emulsion, verfahren zu ihrer herstellung und verwendung derselben
EP0185185B1 (de)	1990-01-24	Verfahren zur Verdunstungshemmung und Mittel zu seiner Durchführung
DE2422954A1 (de)	1975-11-13	Mittel zur reduzierung der drift beim ausbringen waessriger spritzbruehen von pflanzenschutzmitteln
DE69515881T2 (de)	2000-08-17	Pestizide zusammensetzungen, die ethoxylierte fettamine zur steigerung der effektivität von endothall und dessen salzen enthalten.
EP0591768A1 (de)	1994-04-13	Neue Tenside, Verfahren zu ihrer Herstellung, diese enthaltende Mittel und ihre Verwendung
EP0196463B1 (de)	1989-11-15	Makroemulsionen
WO1994010839A1 (de)	1994-05-26	Öl-in-wasser-emulsionen
EP0735815B1 (de)	1998-08-12	Öl-in-wasser-emulsionen
EP0107023B1 (de)	1986-12-17	Homogene wässrige Formulierungen
DE69627682T2 (de)	2004-03-18	Insektizidhilfsmittel
DE60214989T2 (de)	2007-05-10	Verwendung von vicinalen 1,2-Diole zur Bekämpfung von Anthropoden
DD202100A5 (de)	1983-08-31	Neue nematizid-zusammensetzung, verfahren zur herstellung und deren verwendung
DD243846A5 (de)	1987-03-18	Makroemulsionen
DE1542941C (de)	1971-12-02	Herbicides Mittel
DE3512916A1 (de)	1986-10-16	Makroemulsionen