JPH0369321B2 - - Google Patents
Info
- Publication number
- JPH0369321B2 JPH0369321B2 JP12494084A JP12494084A JPH0369321B2 JP H0369321 B2 JPH0369321 B2 JP H0369321B2 JP 12494084 A JP12494084 A JP 12494084A JP 12494084 A JP12494084 A JP 12494084A JP H0369321 B2 JPH0369321 B2 JP H0369321B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- synthetic resin
- acid
- spraying
- resin emulsion
- 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
Links
- 239000000839 emulsion Substances 0.000 claims description 34
- 239000000057 synthetic resin Substances 0.000 claims description 22
- 229920003002 synthetic resin Polymers 0.000 claims description 22
- 238000005507 spraying Methods 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 17
- 239000000575 pesticide Substances 0.000 claims description 12
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 9
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 7
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 6
- 238000007334 copolymerization reaction Methods 0.000 claims description 6
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 claims description 4
- 229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 claims description 3
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 claims description 3
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 claims description 3
- 239000004615 ingredient Substances 0.000 claims 1
- 239000008187 granular material Substances 0.000 description 12
- 239000003905 agrochemical Substances 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- 239000000178 monomer Substances 0.000 description 9
- 241000196324 Embryophyta Species 0.000 description 7
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 4
- -1 2-ethylhexyl Chemical group 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 239000012872 agrochemical composition Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 244000141359 Malus pumila Species 0.000 description 2
- 235000011430 Malus pumila Nutrition 0.000 description 2
- 235000015103 Malus silvestris Nutrition 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 2
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000002316 fumigant Substances 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 230000002940 repellent Effects 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- MNCGMVDMOKPCSQ-UHFFFAOYSA-M sodium;2-phenylethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 MNCGMVDMOKPCSQ-UHFFFAOYSA-M 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- FKOZPUORKCHONH-UHFFFAOYSA-N 2-methylpropane-1-sulfonic acid Chemical compound CC(C)CS(O)(=O)=O FKOZPUORKCHONH-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241000341511 Nematodes Species 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000005667 attractant Substances 0.000 description 1
- 229940007550 benzyl acetate Drugs 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000006172 buffering agent Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N dimethylmethane Natural products CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- GSGDTSDELPUTKU-UHFFFAOYSA-N nonoxybenzene Chemical compound CCCCCCCCCOC1=CC=CC=C1 GSGDTSDELPUTKU-UHFFFAOYSA-N 0.000 description 1
- 125000001117 oleyl 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])=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
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000003128 rodenticide Substances 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- BWYYYTVSBPRQCN-UHFFFAOYSA-M sodium;ethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=C BWYYYTVSBPRQCN-UHFFFAOYSA-M 0.000 description 1
- 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
(産業上の利用分野)
本発明は散布用農薬組成物に関するものであ
り、特には農薬成分を特定の組成からなる合成樹
脂エマルジヨンと混合することにより、散布時に
農薬成分が風等の影響で他地域へ飛散するのを防
ぐと共に植物体への該農薬成分の付着固定化を目
的とするものである。
(従来の技術)
粉剤等の農薬は散布時に風の影響等により目的
圃場以外の近接する田畑、家屋、畜舎、池沼など
へ飛散しやすく、このような農薬の飛散は損失と
いう経済的不利にとどまらず周囲の環境に悪影響
を及ぼすものであり、また充分な病害虫防除効果
が得られない原因ともなる。この解決策として粉
剤を顆粒状あるいは粒状に製剤することが試みら
れているが、粉剤が粒状のものになれば当然のこ
とながら植物体への付着性が大幅に低下すること
になり、風雨などにより容易に流失、飛散してし
まい、この場合にも充分な防除効果が得られない
不利がある。
一方蒸発や昇華により気化する殺虫剤、殺菌
剤、忌避剤、その他のくん蒸剤などに関しては、
その効果を一時的なものとせず比較的長い期間に
わたつて平均して持続させる目的で粒状に製剤化
して使用することもすでに知られているが、この
場合には該製剤化された粒状物の植物体の適当な
高さ適当な部位に、風雨に対しても容易に流失、
飛散することのないように、安定に付着させるこ
とが重要な課題となる。
(発明の構成)
本発明者らは従来のかかる不利欠点にかんがみ
鋭意検討の結果、後記する特定の合成樹脂エマル
ジヨンを混合したものが、一般の散布用器具によ
り散布が容易で植物体への付着が確実であり、風
雨による飛散・流失がなく、また気化性農薬等に
ついてはその効果が植物体上で長期間持続される
ことを確認し、本発明を完成した。
本発明で対象とされる農薬としては、粉末状、
粒状、液状、さらには除放性とするためにあらか
じめ製剤化されたものなど各種形態のものが包含
され、また農薬の有効成分についても特に制限は
なく、一般的に殺虫剤、殺菌剤、殺線虫剤、除草
剤、殺そ剤、植物成長調製剤、忌避剤、誘引剤、
くん蒸剤などがあげられる。
つぎに本発明に使用される合成樹脂エマルジヨ
ンは、(イ)99〜70重量%の、アクリル酸もしくはメ
タクリル酸のエステルまたは酢酸ビニルの1種ま
たは2種以上、(ロ)0.5〜15重量%の、アクリル酸、
メタクリル酸またはグリシジルアクリレートの1
種または2種以上、および(ハ)0.5〜15重量%の、
ビニルスルホン酸、スチレンスルホン酸、2−ア
クリルアミド−2−メチルプロパンスルホン酸あ
るいはその塩類の1種または2種以上、を乳化共
重合して得られるものであり、これを各種の農薬
と混合することにより前記諸効果を達成すること
ができる。
前記(イ)成分に相当する単量体としては、アクリ
ル酸やメタクリル酸のメチル、エチル、プロピ
ル、i−プロピル、n−ブチル、i−ブチル、t
−ブチル、ヘキシル、シクロヘキシル、2−エチ
ルヘキシル、ラウリル、ステアリル、オレイル、
エトキシエチルまたはベンジル等のエステル類、
および酢酸ビニルが例示される。
また(ロ)成分に相当する単量体としては、アクリ
ル酸、メタクリル酸、グリシジルアクリレートが
使用される。
さらに(ハ)成分に相当する単量体成分としてはビ
ニルスルホン酸、スチレンスルホン酸、2−アク
リルアミド−2−メチルプロパンスルホン酸、お
よびこれらのナトリウム塩、カリウム塩またはア
ンモニウム塩などが例示される。
以上述べた(イ)成分、(ロ)成分および(ハ)成分の各単
量体はそれぞれ1種のみでも2種以上組み合せて
用いてもよい。
乳化共重合させる際の上記成分の使用割合は、
(イ)成分99〜70重量%、(ロ)成分0.5〜15重量%およ
び(ハ)成分0.5〜15重量%とすることが必要とされ
る。乳化共重合方法は一般的な方法でよく、乳化
剤としてはアニオン系、ノニオン系、カチオン系
の各種界面活性剤が使用され、また重合開始剤と
しては過硫酸カリウム、過硫酸アンモニウム、過
酸化水素、あるいはこれら過酸化物と還元剤とを
組合せたレドツクス系触媒が使用される。なお、
乳化重合系には必要に応じ連鎖移動剤、緩衝剤、
無機塩類など通常乳化重合に使用される重合助剤
を添加してもよい。
このようにして得られる乳化共重合エマルジヨ
ンは、固形分すなわち重合体成分のTgが−10℃
ないし−60℃であることが望ましく、前記した各
成分の使用割合およびこのTgの範囲が外れると
望まれる付着力(接着力)が発揮されない場合が
ある。またこの乳化共重合エマルジヨンを農薬と
混合する場合に固形分濃度は5重量%以上である
ことが好ましく、これ以下であると散布液の粘度
が充分でないために農薬の分散安定性が低下し散
布の際トラブルが生じたり、また植物体への農薬
の付着力が発揮されない場合が生じる。乳化共重
合エマルジヨンのPHについては特に制限はない
が、植物体の薬害を及ぼさないような範囲すなわ
ちPH6〜8のものとして使用することが望まし
い。
農薬と合成樹脂エマルジヨンとの混合割合につ
いては、農薬の種類、形態ならびに合成樹脂エマ
ルジヨンの種類、固形分濃度等によりその適切な
割合が定められるのでこれを画一的に論じること
はできないが、通常は農薬1重量部に対し合成樹
脂エマルジヨンの固形分0.2〜2重量部、水成分
1〜20重量部の範囲となるようにすることが望ま
しい。
なお、前記合成樹脂エマルジヨンには付着性、
接着性をさらに向上させる目的で水溶性セルロー
スエーテル、ポリビニルアルコール、ポリアクリ
ル酸などの増粘剤を併用してもよい。
本発明の農薬組成物を散布する方法は、適用場
所、規模等により、機械による散布、空中散布な
ど適宜の方法によればよく、散布手段の特別の制
限はない。なお、本発明にかかわる該組成物は水
性液であるので駆動力と吐出ノズルを備えた背負
式等の簡便な一般的散布機により容易に散布する
ことができ、一般の農家においてもその取り扱い
に苦労することはない。
つぎに具体的実施例をあげる。
実施例 1
合成樹脂エマルジヨンを下記のように製造し
た。
合成樹脂エマルジヨン(1):
かくはん機、温度計、還流冷却器および窒素ガ
ス導入管を備えた反応容器に、
アクリル酸2−エチルヘキシル 70重量部
酢酸ビニル 20 〃
メタクリル酸 9 〃
2−アクリルアミド2−メチルプロパンスルホン
酸ナトリウム 1 〃
ポリエチレングリコールノニルフエニルエーテル
(HLB17) 2 〃
ラウリル硫酸ナトリウム 0.5 〃
過硫酸アンモン 0.2 〃
水 100 〃
を仕込み、窒素気流中でかくはんしつつ70℃で6
時間乳化共重合反応させた。ついで冷却しアンモ
ニア水でPH値で6〜7になるように調整し、粗大
粒子のない安定な合成樹脂エマルジヨンを得た。
このものは固形分含有量50%、PH6.2、粘度200セ
ンチボアズ(25℃、ブルツクフイールド粘度計)、
Tg値−38.3℃であつた。
つぎに、農薬としてダイアジノンを有効成分と
する平均粒子径0.4mmの粒剤を用意し、このもの
100重量部と上記合成樹脂エマルジヨン100重量部
および水500重量部を混合し、散布用農薬組成物
を調製した。
この農薬組成物を(株)共立製の背負式動力散布機
(PD−703E−13型)に仕込み、水平より45°の角
度に固定した1m×1mの大きさのポリエチレン
シート上に2mの距離から散布し、該ポリエチレ
ンシート上にダイアジノン粒剤が付着した数と付
着せずに落下した数とから散布時における付着率
を求めた。
散布時の付着率=a/a+b×100(%)
a:付着した粒剤数
b:落下した粒剤数
また、散布を行ない25℃で5時間乾燥後このダ
イアジノン粒剤付着面に約50/分・m2の条件で
1時間または3時間散水した際の当初の粒剤付着
数に対する残存付着数を調べ、散水後の付着率を
求めた。
散水後の付着率=a′/b′×100(%)
a′:散水後の付着粒剤数
b′:散水前の付着粒剤数
結果はそれぞれ次のとおりであつた。
散布時付着率:99%
散水後付着率
散水1時間後:98%
散水3時間後:96%
実施例 2〜6
合成樹脂エマルジヨン(1)と同様にして下記の各
組成および性状を有する合成樹脂エマルジヨン(2)
〜(6)を得た。
合成樹脂エマルジヨン(2):
(単量体仕込み組成)
アクリル酸2−エチルヘキシル 80重量部
メタクリル酸メチル 10 〃
アクリル酸グリシジル 5 〃
スチレンスルホン酸ナトリウム 5 〃
(性状)
固形分=52%、PH=6.8、
粘度=100センチポアズ(25℃)、
Tg=−50.6℃
合成樹脂エマルジヨン(3):
(単量体仕込み組成)
アクリル酸ブチル 64重量部
メタクリル酸メチル 32重量部
メタクリル酸 3 〃
2−アクリルアミド2−メチルプロパンスルホン
酸ナトリウム 1 〃
(性状)
固形分=50%、PH=6.2、
粘度=350センチポアズ(25℃)、
Tg=−14.8℃
合成樹脂エマルジヨン(4):
(単量体仕込み組成)
アクリル酸2−エチルヘキシル 90重量部
アクリル酸 6 〃
スチレンスルホン酸ナトリウム 4 〃
(性状)
固形分=51%、PH=6.2、
粘度=400センチポアズ(25℃)
Tg=−60℃
合成樹脂エマルジヨン(5):
(単量体仕込み組成)
アクリル酸2−エチルヘキシル 70重量部
酢酸ビニル 16 〃
メタクリル酸 7 〃
ビニルスルホン酸ナトリウム 7 〃
(性状)、
固形分=48%、PH=6.3、
粘度=300センチポアズ(25℃)、
Tg=−40.4℃
合成樹脂エマルジヨン(6):
(単量体仕込み組成)
アクリル酸ブチル 99重量部
アクリル酸 0.5 〃
2−アクリルアミド2−メチルプロパンスルホン
酸ナトリウム 0.5 〃
(性状)
固形分=49%、PH=6.6、
粘度=50センチポアズ(25℃)、
Tg=−54℃
次に実施例1で用いたと同様のダイアジノン粒
剤100重量部と上記いずれかの合成樹脂エマルジ
ヨン100重量部および水500重量部を混合し、各組
成物を調製した。これらについて実施例1と同様
にして散布時付着率(%)および散水後付着率
(%)(散水1時間後および散水3時間後)を測定
したところ、第1表に示すとおりの結果が得られ
た。
(Industrial Application Field) The present invention relates to an agrochemical composition for spraying, and in particular, by mixing agrochemical components with a synthetic resin emulsion having a specific composition, the agrochemical components are dispersed by wind, etc. during spraying. The purpose is to prevent the pesticide components from being dispersed into the area and to fix the pesticide components on the plants. (Conventional technology) When spraying pesticides such as powders, they tend to scatter into nearby fields, houses, livestock barns, ponds, etc. other than the target field due to the influence of wind, etc. Such scattering of pesticides is not only an economic disadvantage in terms of losses. This has a negative impact on the surrounding environment, and also causes insufficient pest control effects. As a solution to this problem, attempts have been made to formulate powders into granules or granules, but if the powders are made into granules, their adhesion to plants will naturally be significantly reduced, and wind, rain, etc. Therefore, it is easily washed away and scattered, and in this case as well, there is a disadvantage that a sufficient pest control effect cannot be obtained. On the other hand, regarding insecticides, fungicides, repellents, and other fumigants that vaporize through evaporation or sublimation,
It is already known that the effect is not temporary and is maintained evenly over a relatively long period of time by being formulated into a granular formulation, but in this case, the granular formulation It can be easily washed away by wind and rain at the appropriate height and appropriate part of the plant.
The important issue is to ensure stable adhesion to prevent scattering. (Structure of the Invention) The present inventors have conducted intensive studies in consideration of the disadvantages of the conventional methods, and have found that a mixture of a specific synthetic resin emulsion described later is easy to spray with a general spraying device and does not adhere to plants. The present invention was completed by confirming that the pesticides are reliable, do not scatter or wash away due to wind and rain, and that the effects of vaporizable pesticides are sustained on plants for a long period of time. The agricultural chemicals targeted by the present invention include powdered,
It includes various forms such as granular, liquid, and even those that have been formulated in advance for sustained release.There are also no particular restrictions on the active ingredients of agricultural chemicals, and they generally include insecticides, fungicides, and pesticides. Nematodes, herbicides, rodenticides, plant growth regulators, repellents, attractants,
Examples include fumigants. Next, the synthetic resin emulsion used in the present invention includes (a) 99 to 70% by weight of one or more esters of acrylic acid or methacrylic acid or vinyl acetate, and (b) 0.5 to 15% by weight. , acrylic acid,
1 of methacrylic acid or glycidyl acrylate
species or two or more species, and (c) 0.5 to 15% by weight,
It is obtained by emulsion copolymerization of one or more of vinyl sulfonic acid, styrene sulfonic acid, 2-acrylamido-2-methylpropanesulfonic acid, or their salts, and can be mixed with various agricultural chemicals. The various effects described above can be achieved. Monomers corresponding to component (a) include methyl, ethyl, propyl, i-propyl, n-butyl, i-butyl, and t-acrylic acid and methacrylic acid.
-butyl, hexyl, cyclohexyl, 2-ethylhexyl, lauryl, stearyl, oleyl,
Esters such as ethoxyethyl or benzyl,
and vinyl acetate. Furthermore, as the monomer corresponding to component (b), acrylic acid, methacrylic acid, and glycidyl acrylate are used. Furthermore, examples of monomer components corresponding to component (iii) include vinylsulfonic acid, styrenesulfonic acid, 2-acrylamido-2-methylpropanesulfonic acid, and their sodium, potassium, or ammonium salts. The monomers of component (a), component (b) and component (c) described above may be used alone or in combination of two or more. The usage ratio of the above components during emulsion copolymerization is:
It is required that component (a) be 99 to 70% by weight, component (b) 0.5 to 15% by weight, and component (c) 0.5 to 15% by weight. The emulsion copolymerization method may be a general method, and various anionic, nonionic, and cationic surfactants are used as emulsifiers, and potassium persulfate, ammonium persulfate, hydrogen peroxide, or A redox catalyst containing a combination of these peroxides and a reducing agent is used. In addition,
In the emulsion polymerization system, chain transfer agents, buffering agents,
Polymerization aids commonly used in emulsion polymerization, such as inorganic salts, may be added. The emulsion copolymer emulsion obtained in this way has a solid content, that is, a Tg of the polymer component of -10°C.
Desirably, the temperature is between -60°C, and if the ratio of each component used and the Tg are out of the ranges described above, the desired adhesion (adhesive force) may not be exhibited. In addition, when this emulsion copolymer emulsion is mixed with agricultural chemicals, it is preferable that the solid content concentration is 5% by weight or more. If it is less than this, the viscosity of the spraying liquid will not be sufficient and the dispersion stability of the agricultural chemicals will decrease, resulting in spraying. Trouble may occur during this process, or the pesticide may not be able to adhere to the plant. There is no particular restriction on the pH of the emulsion copolymerization emulsion, but it is desirable to use it within a range that does not cause any phytotoxicity to plants, that is, a pH of 6 to 8. Regarding the mixing ratio of agricultural chemicals and synthetic resin emulsions, the appropriate ratio is determined by the type and form of the agricultural chemicals as well as the type of synthetic resin emulsion, solid content concentration, etc., so it cannot be discussed uniformly, but usually It is desirable that the solid content of the synthetic resin emulsion be 0.2 to 2 parts by weight and the water component be 1 to 20 parts by weight per 1 part by weight of the agricultural chemical. Note that the synthetic resin emulsion has adhesive properties,
In order to further improve adhesiveness, a thickener such as water-soluble cellulose ether, polyvinyl alcohol, polyacrylic acid, etc. may be used in combination. The method of spraying the agrochemical composition of the present invention may be any suitable method such as mechanical spraying or aerial spraying depending on the application site, scale, etc., and there are no particular restrictions on the spraying means. Furthermore, since the composition according to the present invention is an aqueous liquid, it can be easily sprayed using a simple general sprayer such as a backpack type sprayer equipped with a driving force and a discharge nozzle, and is easy to handle even for ordinary farmers. It's not a struggle. Next, specific examples will be given. Example 1 A synthetic resin emulsion was produced as follows. Synthetic resin emulsion (1): In a reaction vessel equipped with a stirrer, a thermometer, a reflux condenser, and a nitrogen gas inlet tube, 2-ethylhexyl acrylate 70 parts by weight Vinyl acetate 20 methacrylic acid 9 2-methyl 2-acrylamide Sodium propane sulfonate 1 Polyethylene glycol nonyl phenyl ether (HLB17) 2 Sodium lauryl sulfate 0.5 Ammonium persulfate 0.2 Water 100% and stirred in a nitrogen stream at 70°C.
A time emulsion copolymerization reaction was carried out. The mixture was then cooled and adjusted to a pH value of 6 to 7 with aqueous ammonia to obtain a stable synthetic resin emulsion free of coarse particles.
This product has a solid content of 50%, a pH of 6.2, a viscosity of 200 centiboads (25°C, Burdskfield viscometer),
The Tg value was -38.3°C. Next, we prepared granules with an average particle size of 0.4 mm containing diazinon as an active ingredient as a pesticide.
A pesticide composition for spraying was prepared by mixing 100 parts by weight of the above synthetic resin emulsion and 500 parts by weight of water. This agrochemical composition was loaded into a backpack-type power spreader (model PD-703E-13) manufactured by Kyoritsu Co., Ltd., and spread at a distance of 2 m on a polyethylene sheet measuring 1 m x 1 m fixed at an angle of 45° from the horizontal. The adhesion rate was determined from the number of diazinon granules that adhered to the polyethylene sheet and the number that fell without adhering to the polyethylene sheet. Adhesion rate during spraying = a/a+b×100 (%) a: Number of adhered granules b: Number of fallen granules In addition, after spraying and drying at 25°C for 5 hours, approximately 50% of the diazinon granules adhered to the surface When water was sprinkled for 1 hour or 3 hours under the conditions of 1 min/m 2 , the number of remaining particles attached to the initial number of particles attached was examined, and the adhesion rate after watering was determined. Adhesion rate after watering = a'/b' x 100 (%) a': Number of adhered granules after watering b': Number of adhered granules before watering The results were as follows. Adhesion rate during spraying: 99% Adhesion rate after watering 1 hour after watering: 98% 3 hours after watering: 96% Examples 2 to 6 Synthetic resins having the following composition and properties in the same manner as synthetic resin emulsion (1) Emulsion (2)
~(6) was obtained. Synthetic resin emulsion (2): (Monomer composition) 2-ethylhexyl acrylate 80 parts by weight Methyl methacrylate 10 Glycidyl acrylate 5 Sodium styrene sulfonate 5 (Properties) Solid content = 52%, PH = 6.8 , Viscosity = 100 centipoise (25℃), Tg = -50.6℃ Synthetic resin emulsion (3): (Monomer preparation composition) Butyl acrylate 64 parts by weight Methyl methacrylate 32 parts by weight Methacrylic acid 3 〃 2-Acrylamide 2- Sodium methylpropanesulfonate 1 〃 (Properties) Solid content = 50%, PH = 6.2, Viscosity = 350 centipoise (25℃), Tg = -14.8℃ Synthetic resin emulsion (4): (Monomer preparation composition) Acrylic acid 2-Ethylhexyl 90 parts by weight Acrylic acid 6 Sodium styrene sulfonate 4 (Properties) Solid content = 51%, PH = 6.2, Viscosity = 400 centipoise (25℃) Tg = -60℃ Synthetic resin emulsion (5): ( Monomer charge composition) 2-ethylhexyl acrylate 70 parts by weight Vinyl acetate 16 〃 Methacrylic acid 7 〃 Sodium vinylsulfonate 7 〃 (Properties) Solid content = 48%, PH = 6.3, Viscosity = 300 centipoise (25℃) , Tg=-40.4℃ Synthetic resin emulsion (6): (Monomer preparation composition) Butyl acrylate 99 parts by weight Acrylic acid 0.5 〃 Sodium 2-acrylamide 2-methylpropanesulfonate 0.5 〃 (Properties) Solid content = 49% , PH = 6.6, viscosity = 50 centipoise (25°C), Tg = -54°C Next, 100 parts by weight of diazinon granules similar to those used in Example 1, 100 parts by weight of any of the above synthetic resin emulsions, and 500 parts by weight of water. Each composition was prepared by mixing the following parts. When the adhesion rate (%) during spraying and the adhesion rate (%) after watering (1 hour after watering and 3 hours after watering) were measured for these in the same manner as in Example 1, the results shown in Table 1 were obtained. It was done.
【表】
比較例 1
実施例1において、合成樹脂エマルジヨン(1)の
代りに酢酸ビニル樹脂エマルジヨン〔コニシ(株)
製、ボンドCH−18〕を同じ使用割合で使用した
ほかは同様にして散布実験を行つた。散布時の付
着率は98%であつたが、散水1時間後の付着率は
22%と低く、さらに散水3時間後の付着率は1%
でありほとんどが脱落・流失し、充分な付着力を
示さなかつた。
実施例 7
実施例1で調製した、ダイアジノン粒剤と合成
樹脂エマルジヨン(1)とからなる組成物を、樹高4
mのリンゴの木に散布して1カ月後の残存付着率
(%)
残存付着率=30日後の付着数/初期付着数×100(%
)
を調べた。この試験期間中降雨のあつた日数は5
日間であつたが、1カ月放置後の付着率は88%で
あり良好な付着性能を示した。
比較例 2
比較例1と同様の散布組成物を、実施例7の試
験と並行してリンゴの木に散布し、1カ月後の残
存付着率を調べた。最初の降雨日の後の付着率が
すでに38%と低く、1カ月放置後ではほとんどが
脱落しており充分な付着力を示さなかつた。[Table] Comparative Example 1 In Example 1, vinyl acetate resin emulsion [Konishi Co., Ltd.] was used instead of synthetic resin emulsion (1).
Spraying experiments were conducted in the same manner except that Bond CH-18] (manufactured by BOND CH-18) was used at the same rate. The adhesion rate at the time of spraying was 98%, but the adhesion rate after 1 hour of watering was
The adhesion rate is as low as 22%, and the adhesion rate after 3 hours of watering is 1%.
Most of it fell off or was washed away, and did not exhibit sufficient adhesion. Example 7 The composition prepared in Example 1, consisting of diazinon granules and synthetic resin emulsion (1), was
Residual adhesion rate (%) one month after spraying on apple trees of m
) was investigated. The number of rainy days during this test period was 5.
The adhesion rate after being left for one month was 88%, indicating good adhesion performance. Comparative Example 2 The same spray composition as in Comparative Example 1 was sprayed on apple trees in parallel with the test in Example 7, and the residual adhesion rate after one month was examined. The adhesion rate after the first rainy day was already low at 38%, and after being left for one month, most of it had fallen off and did not show sufficient adhesion.
Claims (1)
もしくはメタクリル酸のエステルまたは酢酸ビニ
ルの1種または2種以上、(ロ)0.5〜15重量%の、
アクリル酸、メタクリル酸またはグリシジルアク
リレートの1種または2種以上、および(ハ)0.5〜
15重量%の、ビニルスルホン酸、スチレンスルホ
ン酸、2−アクリルアミド−2−メチルプロパン
スルホン酸あるいはその塩類の1種または2種以
上を乳化共重合して得た合成樹脂エマルジヨンと
からなる散布用農薬組成物。1 Pesticide ingredients, (a) 99 to 70% by weight of one or more esters of acrylic acid or methacrylic acid or vinyl acetate, (b) 0.5 to 15% by weight,
one or more types of acrylic acid, methacrylic acid or glycidyl acrylate, and (c) 0.5~
A pesticide for spraying comprising 15% by weight of a synthetic resin emulsion obtained by emulsion copolymerization of one or more of vinylsulfonic acid, styrenesulfonic acid, 2-acrylamido-2-methylpropanesulfonic acid, or their salts. Composition.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12494084A JPS615001A (en) | 1984-06-18 | 1984-06-18 | Pesticide composition for spraying |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12494084A JPS615001A (en) | 1984-06-18 | 1984-06-18 | Pesticide composition for spraying |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS615001A JPS615001A (en) | 1986-01-10 |
| JPH0369321B2 true JPH0369321B2 (en) | 1991-10-31 |
Family
ID=14897950
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12494084A Granted JPS615001A (en) | 1984-06-18 | 1984-06-18 | Pesticide composition for spraying |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS615001A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014037443A (en) * | 2008-04-25 | 2014-02-27 | Nippon Soda Co Ltd | Granular agrochemical composition and production method of the same |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61291502A (en) * | 1985-06-19 | 1986-12-22 | Shinto Paint Co Ltd | Method for controlling noxious life |
| BRPI0609170A2 (en) * | 2005-03-10 | 2010-11-16 | Basf Ag | processes for producing aqueous polymeric dispersions containing pesticide, and for combating harmful microorganisms and / or for regulating plant growth and / or for combating undesirable plant growth and / or for combating insect infestation or undesirable mites and / or for controlling phytopathogenic fungi and / or to treat seeds, aqueous dispersion, agrochemical formulation, dispersions use, and, seed |
| WO2014010435A1 (en) * | 2012-07-13 | 2014-01-16 | 日本エンバイロケミカルズ株式会社 | Anti-bioactive particles and method for manufacturing same |
-
1984
- 1984-06-18 JP JP12494084A patent/JPS615001A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014037443A (en) * | 2008-04-25 | 2014-02-27 | Nippon Soda Co Ltd | Granular agrochemical composition and production method of the same |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS615001A (en) | 1986-01-10 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |