JPH0517882B2 - - Google Patents
Info
- Publication number
- JPH0517882B2 JPH0517882B2 JP60296588A JP29658885A JPH0517882B2 JP H0517882 B2 JPH0517882 B2 JP H0517882B2 JP 60296588 A JP60296588 A JP 60296588A JP 29658885 A JP29658885 A JP 29658885A JP H0517882 B2 JPH0517882 B2 JP H0517882B2
- Authority
- JP
- Japan
- Prior art keywords
- ethoprophos
- weight
- ethoprofos
- capsule
- capsules
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- 239000002775 capsule Substances 0.000 claims description 69
- 239000005961 Ethoprophos Substances 0.000 claims description 61
- VJYFKVYYMZPMAB-UHFFFAOYSA-N ethoprophos Chemical compound CCCSP(=O)(OCC)SCCC VJYFKVYYMZPMAB-UHFFFAOYSA-N 0.000 claims description 61
- 239000002002 slurry Substances 0.000 claims description 36
- 239000000203 mixture Substances 0.000 claims description 21
- 239000003094 microcapsule Substances 0.000 claims description 17
- 239000012528 membrane Substances 0.000 claims description 14
- 229920001807 Urea-formaldehyde Polymers 0.000 claims description 10
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 10
- 239000008158 vegetable oil Substances 0.000 claims description 10
- 229920000877 Melamine resin Polymers 0.000 claims description 9
- 238000004090 dissolution Methods 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 9
- 239000000843 powder Substances 0.000 claims description 9
- 239000011162 core material Substances 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 239000002270 dispersing agent Substances 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 5
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 claims description 5
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
- 230000000052 comparative effect Effects 0.000 description 16
- 238000012360 testing method Methods 0.000 description 16
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 14
- 239000008187 granular material Substances 0.000 description 13
- 238000005538 encapsulation Methods 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 10
- 230000001069 nematicidal effect Effects 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 239000002245 particle Substances 0.000 description 9
- 231100000419 toxicity Toxicity 0.000 description 9
- 230000001988 toxicity Effects 0.000 description 9
- 239000000243 solution Substances 0.000 description 8
- 239000002689 soil Substances 0.000 description 7
- 230000032683 aging Effects 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical compound NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 description 5
- 125000002091 cationic group Chemical group 0.000 description 5
- 238000010828 elution Methods 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 5
- 239000011259 mixed solution Substances 0.000 description 5
- 239000005645 nematicide Substances 0.000 description 5
- VGGLHLAESQEWCR-UHFFFAOYSA-N N-(hydroxymethyl)urea Chemical compound NC(=O)NCO VGGLHLAESQEWCR-UHFFFAOYSA-N 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- 239000004202 carbamide Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000004945 emulsification Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 3
- 241000699670 Mus sp. Species 0.000 description 3
- 241000244206 Nematoda Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000008186 active pharmaceutical agent Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229940088679 drug related substance Drugs 0.000 description 3
- 239000003549 soybean oil Substances 0.000 description 3
- 235000012424 soybean oil Nutrition 0.000 description 3
- 241000258920 Chilopoda Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 244000017020 Ipomoea batatas Species 0.000 description 2
- 235000002678 Ipomoea batatas Nutrition 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 235000012343 cottonseed oil Nutrition 0.000 description 2
- 239000002385 cottonseed oil Substances 0.000 description 2
- 230000007682 dermal toxicity Effects 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- -1 fatty acid salts Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 239000004006 olive oil Substances 0.000 description 2
- 235000008390 olive oil Nutrition 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 239000008262 pumice Substances 0.000 description 2
- 231100000438 skin toxicity Toxicity 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- AKTDWFLTNDPLCH-UHFFFAOYSA-N 1,1,3,3-tetrakis(hydroxymethyl)urea Chemical compound OCN(CO)C(=O)N(CO)CO AKTDWFLTNDPLCH-UHFFFAOYSA-N 0.000 description 1
- ZDTVBVUHESZSGN-UHFFFAOYSA-N 1,1-diaminoethanol Chemical compound CC(N)(N)O ZDTVBVUHESZSGN-UHFFFAOYSA-N 0.000 description 1
- IAUKWGFWINVWKS-UHFFFAOYSA-N 1,2-di(propan-2-yl)naphthalene Chemical compound C1=CC=CC2=C(C(C)C)C(C(C)C)=CC=C21 IAUKWGFWINVWKS-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- SQSPRWMERUQXNE-UHFFFAOYSA-N Guanylurea Chemical compound NC(=N)NC(N)=O SQSPRWMERUQXNE-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
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 244000292697 Polygonum aviculare Species 0.000 description 1
- 235000006386 Polygonum aviculare Nutrition 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 231100000605 Toxicity Class Toxicity 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- YGCOKJWKWLYHTG-UHFFFAOYSA-N [[4,6-bis[bis(hydroxymethyl)amino]-1,3,5-triazin-2-yl]-(hydroxymethyl)amino]methanol Chemical compound OCN(CO)C1=NC(N(CO)CO)=NC(N(CO)CO)=N1 YGCOKJWKWLYHTG-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 231100000293 acute skin toxicity Toxicity 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000013590 bulk material Substances 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 230000000214 effect on organisms Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000003979 granulating agent Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000002602 strong irritant Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- 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
- A01N25/26—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 in coated particulate form
- A01N25/28—Microcapsules or nanocapsules
-
- 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
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
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)
- Manufacturing Of Micro-Capsules (AREA)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60296588A JPS62149607A (ja) | 1985-12-25 | 1985-12-25 | エトプロホスのカプセル剤 |
IT8622870A IT1228244B (it) | 1985-12-25 | 1986-12-24 | Preparato attivo microincapsulato di ethoprophos |
FR8618170A FR2591857A1 (fr) | 1985-12-25 | 1986-12-24 | Ethoprophos microencapsule. |
KR1019860011274A KR900006515B1 (ko) | 1985-12-25 | 1986-12-24 | 에토프로포스의 마이크로캡슐제 |
PH34669A PH23583A (en) | 1985-12-25 | 1986-12-24 | Microencapsulated agent of ethoprophos |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60296588A JPS62149607A (ja) | 1985-12-25 | 1985-12-25 | エトプロホスのカプセル剤 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62149607A JPS62149607A (ja) | 1987-07-03 |
JPH0517882B2 true JPH0517882B2 (it) | 1993-03-10 |
Family
ID=17835485
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60296588A Granted JPS62149607A (ja) | 1985-12-25 | 1985-12-25 | エトプロホスのカプセル剤 |
Country Status (5)
Country | Link |
---|---|
JP (1) | JPS62149607A (it) |
KR (1) | KR900006515B1 (it) |
FR (1) | FR2591857A1 (it) |
IT (1) | IT1228244B (it) |
PH (1) | PH23583A (it) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63178840A (ja) * | 1987-01-19 | 1988-07-22 | Toppan Moore Co Ltd | 徐放性マイクロカプセル |
AU605698B2 (en) * | 1988-11-08 | 1991-01-17 | Kureha Kagaku Kogyo Kabushiki Kaisha | Insecticide comprising a suspension of microcapsule including chlorpyrifos |
US5462915A (en) * | 1989-09-28 | 1995-10-31 | Sandoz Ltd. | Process for producing microcapsules |
JPH04502016A (ja) * | 1989-09-28 | 1992-04-09 | サンド・リミテッド | マイクロカプセルに封入した農薬 |
JPH04310233A (ja) * | 1991-04-05 | 1992-11-02 | Kureha Chem Ind Co Ltd | 湿潤時に芯物質放出性を有するマイクロカプセル |
US5576008A (en) * | 1991-07-19 | 1996-11-19 | Industrial Technology Research Institute | Preparation of pesticide microcapsule |
HUT77708A (hu) | 1994-11-16 | 1998-07-28 | Fmc Corporation | Alacsony illékonyságú clomazone-készítmények |
EP1100336B1 (en) | 1998-07-30 | 2004-02-18 | Fmc Corporation | Microencapsulation formulations of cadusafos |
US6506397B1 (en) | 1999-02-19 | 2003-01-14 | Curt Thies | Pest controlling |
KR100753471B1 (ko) * | 2001-09-06 | 2007-08-31 | 주식회사 엘지생활건강 | 트리클로산을 포함하는 마이크로 캡슐의 제조방법 |
IL148693A0 (en) * | 2002-03-14 | 2002-09-12 | Agrichem Ltd | Encapsulated nematocides |
EP2403332A1 (en) * | 2009-03-04 | 2012-01-11 | Dow AgroSciences LLC | Microencapsulated insecticide with enhanced residual activity |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58124705A (ja) * | 1982-01-18 | 1983-07-25 | Kureha Chem Ind Co Ltd | マイクロカプセル化農薬及びその製造方法 |
-
1985
- 1985-12-25 JP JP60296588A patent/JPS62149607A/ja active Granted
-
1986
- 1986-12-24 KR KR1019860011274A patent/KR900006515B1/ko not_active IP Right Cessation
- 1986-12-24 IT IT8622870A patent/IT1228244B/it active
- 1986-12-24 PH PH34669A patent/PH23583A/en unknown
- 1986-12-24 FR FR8618170A patent/FR2591857A1/fr not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
KR900006515B1 (ko) | 1990-09-03 |
PH23583A (en) | 1989-09-11 |
JPS62149607A (ja) | 1987-07-03 |
IT1228244B (it) | 1991-06-05 |
FR2591857A1 (fr) | 1987-06-26 |
KR870005578A (ko) | 1987-07-06 |
IT8622870A0 (it) | 1986-12-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA1189448A (en) | Microencapsulated agricultural chemical and process of preparation thereof | |
EP0017409B1 (en) | Encapsulation by interfacial polycondensation | |
KR20010015572A (ko) | 조절이 용이한 방출 속도를 갖는 마이크로캡슐 | |
EP0008207B1 (en) | Insecticidal compositions, and preparation and use thereof | |
KR100420287B1 (ko) | 마이크로 캡슐화 된 살충제의 건조된 수분산성 조성물의 제조방법 및 그로 부터 제조된 조성물 | |
AP926A (en) | Microencapsulated Compositions | |
JPH0517882B2 (it) | ||
MXPA06014671A (es) | Microcapsulas de liberacion activada del material contenido en su nucleo. | |
HU215771B (hu) | 2-Klór-N-(etoxi-metil)-6'-etil-o-aceto-toluidid herbicidet tartalmazó kapszulák és eljárás előállításukra | |
PL198545B1 (pl) | Mikrokapsułka, wodna zawiesina mikrokapsułek, kompozycja zawierająca mikrokapsułki, zestaw zawierający mikrokapsułki oraz sposób zwalczania szkodnika | |
US5576008A (en) | Preparation of pesticide microcapsule | |
KR20110132354A (ko) | 향상된 잔류 활성을 갖는 마이크로캡슐화 살충제 | |
KR850001266B1 (ko) | 식물독성이 감소된 살충제 조성물의 제법 | |
EP0368576B1 (en) | Insecticide comprising a suspension of microcapsules containing chlorpyrifos | |
EP1100336B1 (en) | Microencapsulation formulations of cadusafos | |
FR2589677A1 (fr) | Procede pour la mise en oeuvre de micro-capsules de pesticides concernant la chimie agricole | |
JP2021123581A (ja) | マイクロカプセル農薬組成物 | |
JPH0229289B2 (it) | ||
JP7550707B2 (ja) | マイクロカプセル農薬組成物 | |
CN112335675B (zh) | 一种含有噻唑膦的农药制剂及其制备方法 | |
KR830001488B1 (ko) | 살충제 조성물의 제조방법 |