JPH0635362B2 - Stable paste pesticide application - Google Patents
Stable paste pesticide applicationInfo
- Publication number
- JPH0635362B2 JPH0635362B2 JP18148685A JP18148685A JPH0635362B2 JP H0635362 B2 JPH0635362 B2 JP H0635362B2 JP 18148685 A JP18148685 A JP 18148685A JP 18148685 A JP18148685 A JP 18148685A JP H0635362 B2 JPH0635362 B2 JP H0635362B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- added
- active ingredient
- room temperature
- pesticide
- 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
- 239000000575 pesticide Substances 0.000 title claims description 16
- 239000011248 coating agent Substances 0.000 claims description 20
- 239000004480 active ingredient Substances 0.000 claims description 18
- 229920000151 polyglycol Polymers 0.000 claims description 15
- 239000010695 polyglycol Substances 0.000 claims description 15
- 239000007788 liquid Substances 0.000 claims description 11
- 235000011837 pasties Nutrition 0.000 claims description 9
- 239000007787 solid Substances 0.000 claims description 9
- 239000000843 powder Substances 0.000 description 17
- 229920001223 polyethylene glycol Polymers 0.000 description 14
- 239000002202 Polyethylene glycol Substances 0.000 description 12
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 10
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 8
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 description 8
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 8
- 235000012239 silicon dioxide Nutrition 0.000 description 8
- 239000005807 Metalaxyl Substances 0.000 description 7
- DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- 239000000945 filler Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 239000003960 organic solvent Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 241000196324 Embryophyta Species 0.000 description 6
- 239000003814 drug Substances 0.000 description 6
- 229940079593 drug Drugs 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 231100000674 Phytotoxicity Toxicity 0.000 description 5
- 201000010099 disease Diseases 0.000 description 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 5
- 229940051250 hexylene glycol Drugs 0.000 description 5
- KRTSDMXIXPKRQR-AATRIKPKSA-N monocrotophos Chemical compound CNC(=O)\C=C(/C)OP(=O)(OC)OC KRTSDMXIXPKRQR-AATRIKPKSA-N 0.000 description 5
- 240000008067 Cucumis sativus Species 0.000 description 4
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 4
- 241000227653 Lycopersicon Species 0.000 description 4
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 4
- 239000003905 agrochemical Substances 0.000 description 4
- 239000008199 coating composition Substances 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000004898 kneading Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000004166 Lanolin Substances 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000004264 Petrolatum Substances 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 235000013871 bee wax Nutrition 0.000 description 3
- 239000012166 beeswax Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000011081 inoculation Methods 0.000 description 3
- 235000019388 lanolin Nutrition 0.000 description 3
- 229940039717 lanolin Drugs 0.000 description 3
- 229940056211 paraffin Drugs 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- 239000003090 pesticide formulation Substances 0.000 description 3
- 229940066842 petrolatum Drugs 0.000 description 3
- 235000019271 petrolatum Nutrition 0.000 description 3
- -1 phosphorus compound Chemical class 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- 239000005813 Penconazole Substances 0.000 description 2
- 229940092738 beeswax Drugs 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 230000002940 repellent Effects 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- OVANCIHPSBMNEN-UHFFFAOYSA-N (2,2-dimethyl-3h-1-benzofuran-7-yl)methylcarbamic acid Chemical compound C1=CC(CNC(O)=O)=C2OC(C)(C)CC2=C1 OVANCIHPSBMNEN-UHFFFAOYSA-N 0.000 description 1
- FPZWZCWUIYYYBU-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl acetate Chemical compound CCOCCOCCOC(C)=O FPZWZCWUIYYYBU-UHFFFAOYSA-N 0.000 description 1
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 241001600408 Aphis gossypii Species 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 241000233622 Phytophthora infestans Species 0.000 description 1
- 241001281805 Pseudoperonospora cubensis Species 0.000 description 1
- 241000124033 Salix Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 244000061458 Solanum melongena Species 0.000 description 1
- 235000002597 Solanum melongena Nutrition 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000012868 active agrochemical ingredient Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000000305 astragalus gummifer gum Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- SFMJNHNUOVADRW-UHFFFAOYSA-N n-[5-[9-[4-(methanesulfonamido)phenyl]-2-oxobenzo[h][1,6]naphthyridin-1-yl]-2-methylphenyl]prop-2-enamide Chemical group C1=C(NC(=O)C=C)C(C)=CC=C1N1C(=O)C=CC2=C1C1=CC(C=3C=CC(NS(C)(=O)=O)=CC=3)=CC=C1N=C2 SFMJNHNUOVADRW-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000009333 weeding Methods 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、農薬有効成分と、常温で液体状であるモノグ
リコール類若しくはポリグリコール類と、常温で固体状
であるポリグリコール類とを配合してなることを特徴と
する安定なペースト状農薬塗布剤に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial field of application] The present invention blends an agrochemical active ingredient, monoglycols or polyglycols that are liquid at room temperature, and polyglycols that are solid at room temperature. The present invention relates to a stable pasty pesticide coating agent characterized by the following.
農薬製剤はその形態により粉剤、乳剤、水和剤、粒剤な
どに分けられる。一般的に、粉剤、乳剤、水和剤などの
散布剤は作物及び防除対象の害虫、病原菌、雑草などに
速やかに到達して速効的な効果を発現するが、その反
面、圃場に均一に散布するために、作物や防除対象に到
達せずに無駄になる薬剤の最も多い。また、人畜に対す
る毒性の強い農薬は散布剤としては使用できず粒剤とし
て使用されるが、一般的に粒剤として土壌表面に処理さ
れた農薬は作物や雑草に吸収された後に効果を発現する
ために遅効的であり、また吸収されずに無駄になる薬剤
の量が散布剤に比して多い。このことは土壌残留の問題
にもつながるものであり、従つて効果、土壌残留及びコ
スト等の面から作物や防除対象に到達せずに無駄になる
薬剤量を可及的に少なくすることが望ましい。Pesticide formulations are classified into powders, emulsions, wettable powders, granules and the like depending on the form. Generally, powders, emulsions, wettable powders, and other spraying agents quickly reach crops and pests to be controlled, pathogens, weeds, etc., and have a rapid-acting effect, but on the other hand, they are uniformly sprayed on the field. Therefore, most of the chemicals are wasted without reaching the crops or the control target. In addition, pesticides that are highly toxic to humans and livestock cannot be used as sprays and are used as granules.Generally, pesticides treated on the soil surface as granules are effective after being absorbed by crops and weeds. Therefore, it is slow-acting, and the amount of the drug that is not absorbed and wasted is larger than that of the spray agent. This leads to the problem of soil retention, and it is therefore desirable to minimize the amount of chemicals wasted without reaching the crops or control targets from the viewpoints of effect, soil retention and cost. .
これらの農薬製剤に対して、植物の樹幹に直接処理する
農薬塗布剤は、作物や防除対象に到達せずに無駄になる
薬剤の量がごく少なく、効果に優れ、土壌残留問題も回
避できる優れた農薬製剤である。In contrast to these pesticide formulations, pesticide coating agents that directly treat the trunks of plants have a very small amount of waste chemicals that do not reach the crops or the control target, are highly effective, and can also avoid soil residue problems. It is a pesticide formulation.
従来の農薬塗布剤は通常アクリル樹脂、塩化ゴム、石油
樹脂、ポリ酢酸ビニル、ポリビニルアルコール、ラテツ
クスエマルジヨン、α−デンプン、ビニル重合体、セル
ロースエーテル類、カルボキシメチルセルロース、トラ
ガントゴム、アラビアゴム等の塗膜形成剤を充てん剤と
ともに水または有機溶媒に混合、分散させてなる。しか
し、該塗布剤の調製に有機溶媒を用いた場合には作物に
対して薬害を引き起こす場合が多く、また水を用いた場
合には成分の安定性に問題を生じ、特に成分のうちの有
機リン剤の安定性が極度に悪化する。Conventional pesticide coating agents are usually acrylic resin, chlorinated rubber, petroleum resin, polyvinyl acetate, polyvinyl alcohol, latex emulsion, α-starch, vinyl polymer, cellulose ethers, carboxymethyl cellulose, tragacanth gum, gum arabic, etc. The film-forming agent is mixed and dispersed in water or an organic solvent together with the filler. However, when an organic solvent is used for the preparation of the coating agent, it often causes phytotoxicity to crops, and when water is used, it causes a problem in the stability of the components, and in particular, the organic solvent The stability of the phosphorus compound is extremely deteriorated.
本発明は、この課題を解決すべく鋭意研究を重ねた結果
なされたものである。The present invention has been made as a result of intensive studies to solve this problem.
本発明のペースト状農薬塗布剤は、農薬有効成分と、常
温で液体状であるモノグリコール類若しくはポリグリコ
ール類と、常温で固体状であるポリグリコール類とを配
合し、必要に応じて他の有機溶媒、界面活性剤、微粉状
充てん剤又は高級アルコール類、パラフイン、ラノリ
ン、ワセリン及びサラシミツロウ等の増量剤などを配合
してなることを特徴とするものである。The pasty pesticide coating composition of the present invention comprises a pesticide active ingredient, monoglycols or polyglycols that are liquid at room temperature, and polyglycols that are solid at room temperature, and if necessary, other An organic solvent, a surfactant, a fine powder filler or a higher alcohol, a filler such as paraffin, lanolin, petrolatum, and beeswax, and the like are blended.
本発明における塗布剤とは、薬剤を作物、樹木、雑草な
どの植物の樹幹に塗布して、殺虫、殺菌、除草、忌避な
どの効果を発揮させることを目的とする農薬製剤を意味
する。The coating agent in the present invention means an agrochemical formulation for the purpose of exerting effects such as insecticidal, bactericidal, weeding, and repellent by applying the drug to the trunks of plants such as crops, trees and weeds.
本発明の塗布剤は作物に対しては全く薬害を示さず、又
有効成分の安定性にも問題のないものである。The coating agent of the present invention shows no phytotoxicity to crops and has no problem with stability of the active ingredient.
本発明で使用できる農薬の有効成分としては常温で固体
又は液体のものであれば良く、殺虫剤、殺菌剤、除草
剤、植物成長調節剤及び忌避剤等が挙げられる。例えば
化合物を例示すれば、下記のものを挙げることができる
が、本発明はこれらに限定されるものではない。The active ingredient of the pesticide that can be used in the present invention may be one that is solid or liquid at room temperature, and includes insecticides, fungicides, herbicides, plant growth regulators and repellents. Examples of the compound include the following, but the present invention is not limited thereto.
ジメチル(E)−1−メチル−2−(メチルカルバモイ
ル)−ビニルホスフエート、(一般名:モノクロトホ
ス) 2,3−ジヒドロ−2,2−ジメチルベンゾフラン−7
−イルメチルカーバメート、(一般名:カルボフラン) (±)−メチルN−(2−メトキシアセチル)−N−
(2,6−キシリル)−DL−アラニネート、(一般
名:メタラキシル) 1−〔2−(2,4−ジクロロフエニル)−n−ペンチ
ル〕−1H−1,2,4−トリアゾール、(一般名:ペ
ンコナゾール) DL−2−アミノ−4−〔ヒドロキシ(メチル)ホスホ
リル〕酪酸、(一般名:グリホシネート) 本発明で使用する常温で液体状のモノグリコール類とし
ては液体状乃至粘稠状のモノグリコール類であれば良
く、例えばエチレングリコール、プロピレングリコー
ル、ヘキシレングリコール又はグリセロール等を挙げる
ことができる。常温で液体状のポリグリコール類として
は液体状乃至粘稠状のポリグリコール類であれば良く、
例えば低重合度のポリエチレングリコール、例えばポリ
エチレングリコール#200(重合度200:平均分子
量として)、#300、#400及び#600等の液体
状ポリエチレングリコール類又はポリプロピレングリコ
ール類等を挙げることができる。これらは単独で又は2
種以上混合して使用することもできる。Dimethyl (E) -1-methyl-2- (methylcarbamoyl) -vinyl phosphate, (generic name: monocrotophos) 2,3-dihydro-2,2-dimethylbenzofuran-7
-Ylmethylcarbamate, (generic name: carbofuran) (±) -methyl N- (2-methoxyacetyl) -N-
(2,6-xylyl) -DL-alaninate, (generic name: metalaxyl) 1- [2- (2,4-dichlorophenyl) -n-pentyl] -1H-1,2,4-triazole, (general Name: Penconazole) DL-2-amino-4- [hydroxy (methyl) phosphoryl] butyric acid, (general name: glyphosinate) As the monoglycols used in the present invention which are liquid at room temperature, liquid or viscous monoglycols are used. Any glycol can be used, and examples thereof include ethylene glycol, propylene glycol, hexylene glycol, and glycerol. The liquid polyglycols at room temperature may be liquid or viscous polyglycols,
For example, polyethylene glycol having a low degree of polymerization, such as polyethylene glycol # 200 (degree of polymerization 200: as an average molecular weight), liquid polyethylene glycols such as # 300, # 400, and # 600, polypropylene glycols and the like can be mentioned. These alone or 2
It is also possible to use a mixture of two or more species.
本発明で使用する常温で固体状のポリグリコール類とし
ては例えば高重合度のポリエチレングリコール、例えば
ポリエチレングリコール#1000(重合度1000:
平均分子量として)、#1540、#2000、#40
00、#6000及び#20000等の固体状ポリエチ
レングリコール類を挙げることができる。Examples of the polyglycols which are solid at room temperature used in the present invention include polyethylene glycol having a high degree of polymerization, for example, polyethylene glycol # 1000 (degree of polymerization 1000:
(As average molecular weight), # 1540, # 2000, # 40
Solid polyethylene glycols such as 00, # 6000 and # 2000 can be mentioned.
本発明で使用できる有機溶媒としては、ペースト基剤及
び農薬の有効成分に親和性があり、しかも作物に薬害を
与えず、有効成分の安定性を悪化させないものであれば
良く、例えばセロソルブ類、カルビトール類、ジメチル
スルホキシド、ジメチルホルムアミド、有機酸エステル
類、ケトン類などが使用できる。The organic solvent that can be used in the present invention, as long as it has an affinity for the active ingredients of the paste base and agricultural chemicals, does not harm the crops, and does not deteriorate the stability of the active ingredient, for example, cellosolves, Carbitols, dimethylsulfoxide, dimethylformamide, organic acid esters, ketones and the like can be used.
界面活性剤としては、農薬に慣用される非イオン系、ア
ニオン系界面活性剤などが使用できる。As the surfactant, nonionic or anionic surfactants commonly used for agricultural chemicals can be used.
微粉状充てん剤としては、農薬粉剤、粒剤などに慣用さ
れるクレー、ベンナイト、カオリナイト、タルク、炭酸
カルシウム、石膏、珪藻土、合成含水ケイ酸等の微粉が
使用できる。As the fine powdery filler, fine powders such as clay, bentonite, kaolinite, talc, calcium carbonate, gypsum, diatomaceous earth, and synthetic hydrous silicic acid which are commonly used in pesticide powders and granules can be used.
本発明における農薬有効成分、常温で液体状のモノグリ
コール類若しくはポリグリコール類及び常温で固体状の
ポリグリコール類の夫々の割合は有効成分の物理性や他
の添加剤の量によつて適宜変動するが、製剤に対する重
量%で示すと農薬有効成分の割合は0.01%〜90%
の範囲から、常温で液体状のモノグリコール類若しくは
ポリグリコール類の割合は5%〜95%の範囲から、及
び常温で固体状のポリグリコール類の割合は5%〜80
%の範囲から夫々適宜選択すれば良く、さらに必要に応
じてこれらに、有機溶媒、界面活性剤、微粉状充てん剤
又は高級アルコール類、パラフイン、ワセリン、ラノリ
ン及びサラシミツロウ等の増量剤等を適宜の割合で配合
すれば良い。The respective proportions of the pesticide active ingredient in the present invention, the monoglycols or polyglycols which are liquid at room temperature and the polyglycols which are solid at room temperature are appropriately changed depending on the physical properties of the active ingredient and the amount of other additives. However, the ratio of pesticide active ingredient is 0.01% to 90% when expressed in% by weight based on the formulation.
From the range of 5% to 95% of the liquid-state monoglycols or polyglycols at room temperature, and from 5% to 80% of the solid polyglycols at room temperature.
% May be appropriately selected from the range, and if necessary, an organic solvent, a surfactant, a fine powder filler or a higher alcohol, a filler such as paraffin, petrolatum, lanolin and salix beeswax may be appropriately added. It may be mixed in the ratio of.
本発明のペースト状農薬塗布剤の製造方法として、例え
ば、常温で液体状のモノグリコール類若しくはポリグリ
コール類及び常温で固体状のポリグリコール類、更に必
要に応じて界面活性剤又は高級アルコール類、パラフイ
ン、ワセリン、ラノリン及びサラシミツロウ等の増量剤
等を添加混合し40〜100℃に加温溶融させた後、加
温を止め、農薬有効成分及び必要に応じ有機溶媒、微粉
状充てん剤等を添加し、混合しながら徐々に冷却し粘稠
なペースト状農薬塗布剤を調製する方法を挙げることが
できる。As a method for producing the pasty pesticide coating composition of the present invention, for example, liquid monoglycols or polyglycols at room temperature and polyglycols solid at room temperature, further surfactants or higher alcohols as necessary, After adding and mixing extenders such as paraffin, petrolatum, lanolin, and beeswax, and heating and melting at 40 to 100 ° C, stop heating and add active ingredients of pesticide and organic solvent, fine powder filler, etc. as necessary. A method of preparing a viscous pasty agricultural chemical coating agent by adding and mixing and gradually cooling it can be mentioned.
以下に本発明の実施例及び試験例を挙げるが本発明はこ
れらに限定されるものではない。Examples and test examples of the present invention will be given below, but the present invention is not limited thereto.
実施例1 モノクロトホス12.5部にヘキシレングリコール14部を加
え、撹拌して完全に溶解した。別にポリエチレングリコ
ール#400 40部とポリエチレングリコール#40
00 33.5部を混合撹拌しながら60〜80℃に加
温し、溶融させた。完全に溶融した時点で加温をやめ、
これに上記のモノクロトホス・ヘキシレングリコール溶
液を加え、撹拌、混練しながら徐々に冷却して有効成分
12.5%のペースト状塗布剤を得た。Example 1 14 parts of hexylene glycol was added to 12.5 parts of monocrotophos and stirred to dissolve completely. Separately, 40 parts of polyethylene glycol # 400 and polyethylene glycol # 40
33.5 parts of 00 were heated to 60 to 80 ° C. while being mixed and stirred to be melted. Stop heating when completely melted,
The above monocrotophos-hexylene glycol solution was added to this, and the mixture was gradually cooled while stirring and kneading, and the active ingredient was added.
A 12.5% pasty coating agent was obtained.
実施例2 カルボフラン12.5部に合成含水ケイ酸2.5部を加え、
サンプルミル(ホリカワミクロン株式会社製)で粉砕し
てカルボフラン粉末を得た。別にポリエチレングリコー
ル#400 21部、ポリエチレングリコール#400
0 36部及びヘキシレングリコール8部を混合撹拌し
ながら60〜80℃に加温し、溶融させた。これにジメ
チルスルホキシド20部を加えて十分に撹拌・混合した
後、上記のカルボフラン粉末15部を加え、撹拌・混練
しながら徐々に冷却して有効成分12.5%のペースト状塗
布剤を得た。Example 2 To 12.5 parts of carbofuran was added 2.5 parts of synthetic hydrous silicic acid,
A sample mill (manufactured by Horikawa Micron Co., Ltd.) was pulverized to obtain carbofuran powder. Separately, 21 parts of polyethylene glycol # 400, polyethylene glycol # 400
While mixing and stirring 036 parts and 8 parts of hexylene glycol, the mixture was heated to 60 to 80 ° C. and melted. 20 parts of dimethyl sulfoxide was added to this and sufficiently stirred and mixed, and then 15 parts of the above carbofuran powder was added and gradually cooled while stirring and kneading to obtain a paste-like coating agent containing 12.5% of the active ingredient.
実施例3 メタラキシル50部に合成含水ケイ酸50部を加え、サ
ンプルミル(ホリカワミクロン株式会社製)で粉砕して
メタラキシル50%粉末を得た。別にポリエチレングリ
コール#400 35部及びポリエチレングリコール#
4000 35部を混合撹拌しながら60〜80℃に加
温し、溶融させた。これにジメチルスルホキシド20部
と上記のメタラキシル50%粉末10部を加え、撹拌・
混練しながら徐々に冷却して有効成分5%のペースト状
塗布剤を得た。Example 3 50 parts of synthetic hydrous silicic acid was added to 50 parts of metalaxyl and pulverized with a sample mill (manufactured by Horikawa Micron Co., Ltd.) to obtain 50% metalaxyl powder. Separately, 35 parts of polyethylene glycol # 400 and polyethylene glycol #
While mixing and stirring 4000 parts, 4000 parts were heated to 60 to 80 ° C. to be melted. To this, 20 parts of dimethyl sulfoxide and 10 parts of the above metalaxyl 50% powder were added and stirred.
While kneading, the mixture was gradually cooled to obtain a pasty coating agent containing 5% of the active ingredient.
実施例4 ペンコナゾール5部をジメチルスルホキシド20部に溶
解した。別にポリエチレングリコール#400 24
部、ポリエチレングリコール#4000 43部、ヘキ
シレングリコール8部を60〜80℃に加温溶融させ、
これに上記のベンコナゾールのジメチルスルホキシド溶
液を加え、撹拌・混練しながら徐々に冷却して有効成分
5%のペースト状塗布剤を得た。Example 4 5 parts of penconazole were dissolved in 20 parts of dimethyl sulfoxide. Separately polyethylene glycol # 400 24
Part, polyethylene glycol # 4000 43 parts, hexylene glycol 8 parts by heating and melting at 60 to 80 ° C.,
The above-mentioned dimethyl sulfoxide solution of benconazole was added thereto, and gradually cooled while stirring and kneading to obtain a pasty coating agent containing 5% of the active ingredient.
比較例1 ポリビニルアルコール4部を65.5部の水に溶解し、さら
にモノクロトホス12.5部を加えて撹拌し、溶解した。こ
れに合成含水ケイ酸18部を加え、混練して有効成分1
2.5%のペースト状塗布剤を得た。Comparative Example 1 4 parts of polyvinyl alcohol was dissolved in 65.5 parts of water, and 12.5 parts of monocrotophos was further added and stirred to dissolve. To this, 18 parts of synthetic hydrous silicic acid was added and kneaded to prepare the active ingredient 1
A 2.5% paste-like coating agent was obtained.
比較例2 カルボフラン12.5部に合成含水ケイ酸2.5部を加え
て、サンプルミル(ホソカワミクロン株式会社製)で粉
砕し、カルボフラン粉末を得た。別にポリビニルアルコ
ール4.4部を水66.1部に溶解し、これに上記のカルボ
フラン粉末15部を加え、撹拌しながら合成含水ケイ酸
14.5部を加え、混練して、有効成分12.5%のペースト状
塗布剤を得た。Comparative Example 2 2.5 parts of synthetic hydrous silicic acid was added to 12.5 parts of carbofuran and pulverized with a sample mill (manufactured by Hosokawa Micron Co., Ltd.) to obtain carbofuran powder. Separately, 4.4 parts of polyvinyl alcohol was dissolved in 66.1 parts of water, and 15 parts of the above-mentioned carbofuran powder was added thereto, and the synthetic hydrous silicic acid was stirred.
14.5 parts was added and kneaded to obtain a paste-like coating agent containing 12.5% of the active ingredient.
比較例3 ポリ酢酸ビニル10部にフエニルセロソルブ42.5部を加
え、撹拌して溶解した。これにモノクロトホス12.5部、
クレー35部を加え、混練して有効成分12.5%のペース
ト状塗布剤を得た。Comparative Example 3 42.5 parts of phenyl cellosolve was added to 10 parts of polyvinyl acetate and dissolved by stirring. 12.5 parts of monocrotophos,
35 parts of clay was added and kneaded to obtain a pasty coating agent containing 12.5% of the active ingredient.
比較例4 メタラキシル50部に合成含水ケイ酸50部を加え、サ
ンプルミル(ホソカワミクロン株式会社製)で粉砕して
メタラキシル50%粉末を得た。このメタラキシル50
%粉末10部にエチルセルロース10部、合成含水ケイ
酸9部を加えて混合し、さらにジエチレングリコールモ
ノエチルエーテルアセテート71部を加えて混練し、有
効成分5%のペースト状塗布剤を得た。Comparative Example 4 50 parts of synthetic hydrous silicic acid was added to 50 parts of metalaxyl and pulverized with a sample mill (manufactured by Hosokawa Micron Co., Ltd.) to obtain 50% metalaxyl powder. This metalaxyl 50
% 10 parts of powder, 10 parts of ethyl cellulose and 9 parts of synthetic hydrous silicic acid were added and mixed, and further 71 parts of diethylene glycol monoethyl ether acetate was added and kneaded to obtain a paste-like coating agent containing 5% of the active ingredient.
試験例1 安定性試験 本発明の実施例1,2,3及び4のペースト状塗布剤及
び比較例1,2,3及び4のペースト状塗布剤をそれぞ
れガラス製密閉容器に入れ、40℃の恒温器に15日間
及び30日間置いた。その後それぞれの成分濃度を測定
し、調整直後の成分濃度と比較して成分残存率を求め
た。その結果を第1表に示す。Test Example 1 Stability Test The paste-like coating agents of Examples 1, 2, 3 and 4 of the present invention and the paste-like coating agents of Comparative Examples 1, 2, 3 and 4 were placed in glass closed containers at 40 ° C., respectively. It was placed in an incubator for 15 days and 30 days. After that, the respective component concentrations were measured and compared with the component concentrations immediately after the adjustment to obtain the component residual rate. The results are shown in Table 1.
試験例2 効果及び薬害試験 本発明の実施例1,2,3及び4のペースト状塗布剤と
比較例1,2,3及び4のペースト状塗布剤を第5葉期
のナス(品種:千両)の茎部に植物1個体当り100mg
(成分量12.5mg)塗布した。薬剤処理の7日後及び21
日後にワタアブラムシ3齢幼虫を接種し、接種1日後に
その生存を確め死虫率を求めた。又薬剤処理21日後に
薬害の程度を観察し下記の基準に従つて判定した。 Test Example 2 Effect and phytotoxicity test The paste-like coating agents of Examples 1, 2, 3 and 4 of the present invention and the paste-like coating agents of Comparative Examples 1, 2, 3 and 4 were used at the fifth leaf stage eggplant (variety: 1,000 units). ) Stem part 100mg per plant
(Component amount 12.5 mg) was applied. 7 days after drug treatment and 21
One day after the inoculation, the third-instar larva of Aphis gossypii was inoculated, and one day after the inoculation, its survival was confirmed and the mortality rate was calculated. After 21 days from drug treatment, the degree of drug damage was observed and judged according to the following criteria.
+;薬害なし ±;葉縁部のごく一部が褐変又は黄変 +;葉縁部の一部が褐変又は黄変 ;葉縁部の半分程度が褐変又は黄変 ;葉縁部の半分程度が褐斑又は黄斑 ;枯死 その結果を第2表に示す。+: No phytotoxicity ±: A small part of the leaf edge is browned or yellowed +: A part of the leaf edge is browned or yellowed; About half of the leaf edge is browned or yellowed; About half of the leaf edge Is brown spot or yellow spot; withered. The results are shown in Table 2.
試験例3 キユウリベと病及びトマト疾病に対する防除
効果試験 本発明の実施例3のペースト状塗布剤と、対照として比
較例4のペースト状塗布剤を第5葉期のキユウリ(品
種:北進)及び第5葉期のトマト(品種:福寿2号)の
茎基部に所定量塗布した。薬剤処理の7日後にキユウリ
にはキユウリベと病菌(Pseudoperonospora cubensis)、
トマトにはトマト疾病菌(Phytophthora infestans)をそ
れぞれ接種した。接種7日後に発病程度を調査して防除
価を算出した。又同時にキユウリに付いて薬害程度を観
察し、試験例2と同一の基準より判定した。その結果を
第3表に示す。 Test Example 3 Control effect test against cucumber bean disease and tomato disease The paste-form coating composition of Example 3 of the present invention and the paste-form coating composition of Comparative Example 4 as a control were used as the fifth leaf stage of Cucumber (variety: Hokushin) and A predetermined amount was applied to the stem base of a 5-leaf stage tomato (variety: Fukuju No. 2). Seven days after the treatment with the drug, the yellow cucumber and the disease fungus (Pseudoperonospora cubensis)
Each tomato was inoculated with the tomato disease fungus (Phytophthora infestans). Seven days after the inoculation, the degree of disease was investigated and the control value was calculated. At the same time, the degree of phytotoxicity on the cucumber was observed and judged based on the same criteria as in Test Example 2. The results are shown in Table 3.
Claims (1)
グリコール類若しくはポリグリコール類と、常温で固体
状であるポリグリコール類とを配合してなることを特徴
とする安定なペースト状農薬塗布剤。1. A stable pasty pesticide characterized by comprising an active ingredient of pesticide, a monoglycol or a polyglycol which is liquid at room temperature, and a polyglycol which is solid at room temperature. Coating agent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18148685A JPH0635362B2 (en) | 1985-08-19 | 1985-08-19 | Stable paste pesticide application |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18148685A JPH0635362B2 (en) | 1985-08-19 | 1985-08-19 | Stable paste pesticide application |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6242902A JPS6242902A (en) | 1987-02-24 |
JPH0635362B2 true JPH0635362B2 (en) | 1994-05-11 |
Family
ID=16101602
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18148685A Expired - Lifetime JPH0635362B2 (en) | 1985-08-19 | 1985-08-19 | Stable paste pesticide application |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0635362B2 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0764684B2 (en) * | 1990-07-24 | 1995-07-12 | ヤシマ産業株式会社 | Insecticidal / insect-containing ointment and method for producing the same |
DE19506095A1 (en) * | 1994-03-04 | 1995-09-21 | Bayer Agrochem Kk | Paste compsn. contg. pesticides or fungicides for use on plants |
FR2718610B1 (en) * | 1994-04-14 | 1996-06-07 | Roussel Uclaf | New pesticide formulations and their preparation process. |
DE19630651A1 (en) * | 1996-07-30 | 1998-04-16 | Paul Habich | Means for controlling flying and / or crawling insects and / or rodents in rooms |
US6216388B1 (en) * | 1998-04-07 | 2001-04-17 | Gene W. Miller | Dissolving polymer plug for introducing nutrients and medicinal materials into tree trunks |
US6180088B1 (en) | 1998-11-17 | 2001-01-30 | Nihon Nohyaku Co., Ltd. | Foamable aerosol agricultural-chemical composition and method of controlling diseases and insect pests |
JP2007246495A (en) * | 2006-03-20 | 2007-09-27 | Mitsui Chemicals Inc | Method for controlling disease and insect pest |
-
1985
- 1985-08-19 JP JP18148685A patent/JPH0635362B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS6242902A (en) | 1987-02-24 |
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