JPH0680504A - Herbicidal formulation and herbicidal method - Google Patents
Herbicidal formulation and herbicidal methodInfo
- Publication number
- JPH0680504A JPH0680504A JP4355527A JP35552792A JPH0680504A JP H0680504 A JPH0680504 A JP H0680504A JP 4355527 A JP4355527 A JP 4355527A JP 35552792 A JP35552792 A JP 35552792A JP H0680504 A JPH0680504 A JP H0680504A
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- Japan
- Prior art keywords
- parts
- herbicidal
- weight
- anionic surfactant
- manufactured
- Prior art date
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Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は除草剤成分に速効性が付
与された除草製剤および除草方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a herbicidal preparation and a herbicidal method in which a herbicidal ingredient has a fast-acting effect.
【0002】[0002]
【従来の技術】これまで乳剤や水和剤などの除草剤製剤
では35〜50重量%の除草性化合物成分に対して、展
着性,分散性,浸透性等を良くして効果を確実にするた
め20〜30重量%の界面活性剤を加えるのが通常であ
る。2. Description of the Related Art Up to now, herbicidal preparations such as emulsions and wettable powders have improved spreadability, dispersibility, penetration and the like for 35 to 50% by weight of herbicidal compound components to ensure their effects. Therefore, it is usual to add 20 to 30% by weight of a surfactant.
【0003】[0003]
【発明が解決しようとする課題】これらの製剤は実地に
使用する場合、水で1000〜2000倍に希釈して、
たとえば、除草剤濃度0.01〜0.025%、界面活
性剤濃度0.01〜0.03%の希薄濃度で、散布され
るが、除草効果は徐々にしか現れず、速効性が充分とは
言い難い。When these preparations are put to practical use, they are diluted 1000 to 2000 times with water,
For example, the herbicides are sprayed at a dilute concentration of 0.01 to 0.025% and a surfactant concentration of 0.01 to 0.03%, but the herbicidal effect only gradually appears and the rapid-acting effect is sufficient. Is hard to say.
【0004】[0004]
【課題を解決するための手段】上記のような欠点を克服
すべく研究を重ねた結果、本発明者らは除草剤成分と各
種陰イオン界面活性剤の1種以上を、従来散布において
実用された来た濃度よりも遙かに高い濃度で、含有する
水性組成物が予想外にも速効性の除草効果を現すことを
知った。As a result of repeated studies to overcome the above-mentioned drawbacks, the present inventors have practically applied one or more herbicidal components and various anionic surfactants in conventional spraying. It has been found that the aqueous composition containing unexpectedly exhibits a fast-acting herbicidal effect at a much higher concentration than the one obtained.
【0005】本発明はこの新知見に基づくもので、除草
剤成分0.1〜20重量%および陰イオン界面活性剤
0.1重量%以上を含有する水性組成物よりなる直接散
布用速効性除草製剤および上記の水性組成物を雑草に散
布することを特徴とする急速除草方法に関する。The present invention is based on this new finding, and is a fast-acting herbicide for direct application, which comprises an aqueous composition containing 0.1 to 20% by weight of a herbicide component and 0.1% by weight or more of an anionic surfactant. It relates to a method for rapid weeding, which comprises applying a formulation and the above-mentioned aqueous composition to weeds.
【0006】本発明の除草製剤に含有される除草剤成分
としては、各種の除草活性化合物が用いられる。これら
の化合物は、たとえば、有機リン系(例、ビアラホス,
グルホシネート),酸アミド系(例、メトラクロール,
DCPA),ダイアジン系(例、ベンタゾン),フェノ
キシ系(例、MCPB,MCPP),カーバメート系
(例、チオベンカルブ),尿素系(例、DCMU,テブ
チウロン),スルホニル尿素系(例、エスプロカル
ブ),トリアジン系(例、シマジン),ダイゾール系
(例、ピラゾキンフェン),芳香族カルボン酸系(例、
TCBA),脂肪酸系(例、テトラピオン)およびビピ
リジリウム系(例、パラコート)などの有機除草剤化合
を包含する。またそれは塩素酸塩剤などの無機除草剤化
合物であってもよい。As the herbicide component contained in the herbicidal preparation of the present invention, various herbicidally active compounds are used. These compounds are, for example, organophosphorus compounds (eg, bialaphos,
Glufosinate), acid amides (eg, metolachlor,
DCPA), diazine type (eg, bentazone), phenoxy type (eg, MCPB, MCPP), carbamate type (eg, thiobencarb), urea type (eg, DCMU, tebutiuron), sulfonylurea type (eg, esprocarb), triazine type. (Eg, simazine), dizole type (eg, pyrazoquinphene), aromatic carboxylic acid type (eg,
TCBA), fatty acid-based (eg, tetrapion) and bipyridylium-based (eg, paraquat) and other organic herbicide compounds are included. It may also be an inorganic herbicide compound such as a chlorate agent.
【0007】本発明の除草製剤における陰イオン界面活
性剤は本発明の目的を阻害しない限りいずれでもよい
が、好ましいのはスルホネート系,サルフェート系およ
びフォスフェート系陰イオン界面活性剤である。以下、
商品名にはR を付する。The anionic surfactant in the herbicidal preparation of the present invention may be any anionic surfactant as long as the object of the present invention is not impaired, but preferred are sulfonate, sulfate and phosphate anionic surfactants. Less than,
Add R to the product name.
【0008】スルホネート系陰イオン界面活性剤として
は、たとえば、ニューコール−290MR 〔ジアルキル
スルホサクシネート、日本乳化剤(株)製〕,ニューコ
ール−210R 〔アルキルベンゼンスルホネート、同上
製〕,ニューカルゲンEP−4MR 〔ジアルキルスルホ
サクシネート・ソーダ塩、竹本油脂(株)製〕,ニュー
カルゲンEP−4CR 〔ジアルキルスルホサクシネート
・ソーダ塩、同上製〕,RY−453WR 〔松本油脂製
薬(株)製〕,RY−349〔同上製〕,ソルポール5
050R 〔ジアルキルエステルスルホン酸塩、東邦化学
工業(株)製〕,ソルポール3047KR 〔同上製〕,
Disrol SHR 〔ビスナフタレンスルホン酸ソー
ダ、同上製〕などが挙げられるが、これらの例に限定さ
れるものではない。Examples of the sulfonate anionic surfactant include Newcol-290M R [dialkylsulfosuccinate, manufactured by Nippon Emulsifier Co., Ltd.], Newcol-210 R [alkylbenzene sulfonate, manufactured by the same], Newkalgen EP. -4M R [dialkylsulfosuccinate soda salt, manufactured by Takemoto Yushi Co., Ltd.], Newkalgen EP-4C R [dialkylsulfosuccinate soda salt, manufactured by the same company], RY-453W R [Matsumoto Yushi-Seiyaku Co., Ltd.] Made], RY-349 [made by the same], Solpol 5
050 R [dialkyl ester sulfonate, manufactured by Toho Chemical Industry Co., Ltd.], Solpol 3047K R [manufactured by the same company],
Examples thereof include Disrol SH R [sodium bisnaphthalene sulfonate, manufactured by the same company], but are not limited to these examples.
【0009】サルフェート系陰イオン界面活性剤として
は、たとえば、パイオニンA−15R 〔オレイン酸高濃
度硫酸化物、竹本油脂(株)製〕,ロート油40R 〔東
邦化学工業(株)製〕,ニューコール240R 〔アルキ
ルジサルフェート、日本乳化剤(株)製〕,ニューコー
ル560SNR 〔同上製〕,ニューコール570SF
〔ポリオキシエチレンアリルエーテルサルフェート、同
上製〕などが挙げられるが、これらの例に限定されるも
のではない。フォスフェート系陰イオン界面活性剤とし
ては、たとえば、パラコールOPR〔アルキルフォスフ
ェート、東邦化学工業(株)製〕,バイオニンA−73
KR〔アルキルフォスフェート、竹本油脂(株)製〕,
パイオニンA−720R 〔ノニルフェニルエーテルフォ
スフェート、同上製〕などが挙げられるが、これらの例
に限定されるものではない。Examples of the sulfate type anionic surfactants include, for example, Pionin A-15 R [highly concentrated oleic acid sulfate, manufactured by Takemoto Yushi Co., Ltd.], funnel oil 40 R [manufactured by Toho Chemical Industry Co., Ltd.], Newcol 240 R [Alkyl disulfate, manufactured by Nippon Emulsifier Co., Ltd.], Newcor 560 SN R [manufactured by the same company], Newcor 570 SF
Examples thereof include [polyoxyethylene allyl ether sulphate, manufactured by the same company], but are not limited to these examples. Examples of the phosphate-based anionic surfactant include, for example, Parachol OP R [alkyl phosphate, manufactured by Toho Chemical Industry Co., Ltd.], BIONIN A-73.
K R [alkyl phosphate, manufactured by Takemoto Yushi Co., Ltd.],
Examples thereof include Pionine A-720 R [nonylphenyl ether phosphate, manufactured by the same company], but are not limited to these examples.
【0010】また、Disrol H12R 〔日本乳化
剤(株)〕のようなポリカルボン型高分子活性剤も用い
られる。Further, a polycarboxylic type polymer activator such as Disrol H12 R [Japan Emulsifier Co., Ltd.] is also used.
【0011】本発明においては、陰イオン界面活性剤の
1種または2種以上が用いられ、除草剤成分1重量部に
対して陰イオン界面活性剤0.2重量部以上が用いられ
る。除草剤成分と陰イオン界面活性剤の好ましい割合は
一般に前者1重量部に対し後者0.2〜200重量部、
さらに好ましくは0.25〜100重量部である。上記
の除草成分および陰イオン界面活性剤は水または水性溶
媒と混和され、除草剤成分0.1〜20重量%、好まし
くは0.1〜4重量%、陰イオン界面活性剤0.1重量
%以上、好ましくは1〜20重量%、さらに好ましくは
1〜10重量%を含有する水性組成物に調製される。In the present invention, one or more anionic surfactants are used, and 0.2 part by weight or more of the anionic surfactant is used for 1 part by weight of the herbicide component. Generally, the preferable ratio of the herbicide component to the anionic surfactant is 0.2 to 200 parts by weight of the latter with respect to 1 part by weight of the former,
More preferably, it is 0.25 to 100 parts by weight. The above herbicidal component and anionic surfactant are mixed with water or an aqueous solvent, and the herbicidal component is 0.1 to 20% by weight, preferably 0.1 to 4% by weight, anionic surfactant 0.1% by weight. The above composition is prepared into an aqueous composition containing preferably 1 to 20% by weight, more preferably 1 to 10% by weight.
【0012】この水性組成物は水で希釈することなくそ
のまま雑草に散布できるレディユースの除草製剤であ
る。This aqueous composition is a ready-use herbicidal formulation which can be applied to weeds without being diluted with water.
【0013】水性組成物には、必要に応じて、リン酸,
ポリリン酸,クエン酸,酒石酸のような安定剤、イソプ
ロピルアルコール,エチレングリコールのような凍結防
止剤を加えてもよく、また、必要に応じ展着剤,湿潤剤
として、石鹸類,ポリオキシアルキルエーテル類,アル
キル硫酸塩類,ポリエチレングリコールエーテル類,ア
ルキルスルホン酸塩類,多価アルコールエーテル類等の
陰イオン系または非イオン系界面活性剤を添加すること
もできる。The aqueous composition may contain phosphoric acid, if necessary.
Stabilizers such as polyphosphoric acid, citric acid and tartaric acid, and antifreezing agents such as isopropyl alcohol and ethylene glycol may be added, and if necessary, soaps, polyoxyalkyl ethers as spreading agents and wetting agents. Anionic or nonionic surfactants such as compounds, alkyl sulfates, polyethylene glycol ethers, alkyl sulfonates, polyhydric alcohol ethers and the like can be added.
【0014】かくして得られる本発明の除草製剤はその
まま散布して急速に雑草を枯死させるばかりでなく、毒
性が極めて少なくて安全である。The herbicidal preparation of the present invention thus obtained is not only sprayed as it is to rapidly kill weeds, but also has very little toxicity and is safe.
【0015】[0015]
【実施例】次に実施例の形で本発明の除草製剤の製造を
説明すると共に試験例に記載される対照製剤の製造を記
す参考例ならびに本発明製剤と対照製剤の効果を比較す
る試験例を示す。EXAMPLES Next, reference examples describing the production of the herbicidal formulation of the present invention in the form of examples and describing the production of the control formulation described in the test examples, and test examples comparing the effects of the present invention formulation and the control formulation Indicates.
【0016】実施例1 常水867部を溶解タンクに仕込み攪拌しながらニュー
カルゲンEP−4MR〔ジアルキルスルホサクシネート
・ソーダ塩、竹本油脂(株)製〕2.5部、TSA−7
30R (ジメチルシリコン油、消泡剤)0.2部を加え
て充分に混合したのち、DCPA0.6部、イソプロピ
ルアルコール10部を加えて溶解させ液剤を得る。Example 1 867 parts of ordinary water was charged into a dissolution tank and stirred while stirring 2.5 parts of New Calgen EP-4M R [dialkylsulfosuccinate soda salt, manufactured by Takemoto Yushi Co., Ltd.], TSA-7.
After 0.2 part of 30 R (dimethyl silicone oil, antifoaming agent) was added and mixed thoroughly, 0.6 part of DCPA and 10 parts of isopropyl alcohol were added and dissolved to obtain a liquid agent.
【0017】実施例2 常水82.4部を溶解タンクに仕込み攪拌しながらニュ
ーカルゲンEP−4CR 〔ジアルキルスルホサクシネー
ト・ソーダ塩、竹本油脂(株)製〕2.0部、TSA−
730R 0.1部を加えて充分混合したのち、グリホサ
ート0.5部、イソプロピルアルコール15部を加えて
溶解させて液剤を得る。Example 2 82.4 parts of ordinary water was charged into a dissolution tank and stirred with Newcalgen EP-4C R [dialkylsulfosuccinate soda salt, manufactured by Takemoto Yushi Co., Ltd.] 2.0 parts, TSA-
After adding 0.1 part of 730 R and thoroughly mixing, 0.5 part of glyphosate and 15 parts of isopropyl alcohol are added and dissolved to obtain a liquid preparation.
【0018】実施例3 常水79.5部を溶解タンクに仕込み攪拌しながらニュ
ーカルゲンEP−4CR 10部、イソプロピルアルコー
ル10部、TSA−730R 0.1部を加えて充分混合
したのちビアラホス0.4部を加えて均一に溶解させて
液剤を得る。Example 3 79.5 parts of ordinary water was charged into a dissolution tank, 10 parts of Newcalgen EP-4C R, 10 parts of isopropyl alcohol, and 0.1 part of TSA-730 R were added with stirring and sufficiently mixed, and then bialaphos. 0.4 parts is added and uniformly dissolved to obtain a liquid agent.
【0019】実施例4 常水81.9部を溶解タンクに仕込み攪拌しながらニュ
ーコール−290MR〔ジアルキルスルホサクシネー
ト、日本乳化剤(株)製〕2.5部、TSA−730R
0.1部を加えて充分に混合したのち、グリホシネート
0.5部、イソプロピルアルコール15部を加えて溶解
させて液剤を得る。Example 4 81.9 parts of ordinary water was charged into a dissolution tank and stirred with Newcol-290M R [dialkylsulfosuccinate, manufactured by Nippon Emulsifier Co., Ltd.] 2.5 parts, TSA-730 R.
After 0.1 part is added and mixed well, 0.5 part of glyphosinate and 15 parts of isopropyl alcohol are added and dissolved to obtain a liquid preparation.
【0020】実施例5 常水85.8部を溶解タンクに仕込み攪拌しながらニュ
ーコール−210R 〔アルキルベンゼンスルホネート、
日本乳化剤(株)製〕3.5部、TSA−730R 0.
2部を加えて充分に混合したのち、DCMU0.3部、
ターバシル0.2部、イソプロピルアルコール10部を
加えて溶解させて液剤を得る。Example 5 85.8 parts of ordinary water was charged into a dissolution tank and stirred with Newcol-210 R [alkylbenzene sulfonate,
Nippon Emulsifier Co., Ltd.] 3.5 parts, TSA-730 R 0.
After adding 2 parts and mixing well, 0.3 parts of DCMU,
0.2 parts of terbacil and 10 parts of isopropyl alcohol are added and dissolved to obtain a liquid agent.
【0021】実施例6 常水86.5部を溶解タンクに仕込み攪拌しながらニュ
ーカルゲンEP−70GR 〔ジオクチルスルホサクシネ
ート、竹本油脂(株)製〕2.5部、TSA−730R
0.5部を加えて充分に混合したのち、グリホサート・
トリメシウム塩酸0.5部、イソプロピルアルコール1
0部を加えて溶解し液剤を得る。Example 6 86.5 parts of ordinary water was charged into a dissolution tank and stirred while stirring 2.5 parts of Newcalgen EP-70G R [Dioctylsulfosuccinate, manufactured by Takemoto Yushi Co., Ltd.], TSA-730 R.
After adding 0.5 parts and mixing thoroughly, glyphosate
0.5 parts trimesium hydrochloride, 1 isopropyl alcohol
0 part is added and dissolved to obtain a liquid preparation.
【0022】実施例7 常水85.8部を溶解タンクに仕込み攪拌しながらニュ
ーカルゲンEP−4MR 〔ジアルキルスルホサクシネー
ト・ソーダ塩、竹本油脂(株)製〕3.5部、TSA−
730R 0.2部を加えて充分に混合したのち、テブチ
ウロン0.5部、イソプロピルアルコール10部を加え
て溶解し液剤を得る。Example 7 85.8 parts of ordinary water was charged into a dissolution tank and stirred while stirring with Newcalgen EP-4M R [dialkyl sulfosuccinate soda salt, manufactured by Takemoto Yushi Co., Ltd.] 3.5 parts, TSA-
730 R ( 0.2 parts) was added and mixed thoroughly, and then tebutyuron (0.5 parts) and isopropyl alcohol (10 parts) were added to dissolve the solution.
【0023】実施例8 常水86.4部を溶解タンクに仕込み攪拌しながらエア
ロールCT−1R 〔ジオクチルスルホサクシネート、東
邦化学工業(株)製〕2.5部、TSA−730R 0.
5部を加えて充分混合したのち、グリホサート0.6
部、イソプロピルアルコール10部を添加、溶解させて
液剤を得る。Example 8 86.4 parts of ordinary water was charged into a dissolution tank and stirred with air roll CT-1 R [dioctyl sulfosuccinate, manufactured by Toho Chemical Industry Co., Ltd.] 2.5 parts, TSA-730 R 0.
After adding 5 parts and mixing well, glyphosate 0.6
Parts and 10 parts of isopropyl alcohol are added and dissolved to obtain a liquid preparation.
【0024】実施例9 常水69.3部を溶解タンクに仕込み攪拌しながらニュ
ーカルゲンEP4C15部、イソプロピルアルコール1
5部、TSA−750R 0.2部を加えて充分攪拌した
のち、ビアラホス0.5部を溶解させて液剤を得る。Example 9 69.3 parts of ordinary water was charged into a dissolution tank and, with stirring, 15 parts of Newkalgen EP4C and 1 part of isopropyl alcohol.
5 parts After sufficiently stirred with 0.2 parts TSA-750 R, to obtain a liquid formulation by dissolving 0.5 parts of bialaphos.
【0025】実施例10 常水864部を溶解タンクに仕込み攪拌しながらエアロ
ールOPR 〔ジオクチルスルホサクシネート、東邦化学
工業(株)製〕2.5部、TSA−730R 0.5部を
加えて充分混合したのち、アトラジン0.6部、イソプ
ロピルアルコール10部を加えて溶解させ液剤を得る。Example 10 864 parts of ordinary water were charged into a dissolution tank and 2.5 parts of air roll OP R [dioctyl sulfosuccinate, manufactured by Toho Chemical Industry Co., Ltd.] and 0.5 part of TSA-730 R were added with stirring. After thoroughly mixing, 0.6 part of atrazine and 10 parts of isopropyl alcohol are added and dissolved to obtain a liquid agent.
【0026】実施例11 常水87.5部を溶解タンクに仕込み攪拌しながらパイ
オニンA−15R 〔オレイン酸高濃度硫化物、竹本油脂
(株)製〕1.5部、TSA−730R 0.2部を加え
て充分に混合したのち、DCPA0.8部とイソプロピ
ルアルコール10部を加えて溶解させ液剤を得る。Example 11 87.5 parts of ordinary water was charged into a dissolution tank and stirred while stirring, Pionin A-15 R [high concentration oleic acid sulfide, manufactured by Takemoto Yushi Co., Ltd.] 1.5 parts, TSA-730 R 0 After adding 2 parts and thoroughly mixing, 0.8 parts of DCPA and 10 parts of isopropyl alcohol are added and dissolved to obtain a liquid agent.
【0027】実施例12 常水84.2部を溶解タンクに仕込み攪拌しながらフォ
スファノールRP−710R 〔フェノールエーテルリン
酸エステル、東邦化学工業(株)製〕4.5部、TSA
−730R 0.5部を加えて充分に混合したのち、グリ
ホサート・トリメシウム塩酸0.8部とイソプロピルア
ルコール10部を加えて溶解させ液剤を得る。Example 12 84.2 parts of ordinary water was charged into a dissolution tank, and while stirring, phosphanol RP-710 R [phenol ether phosphate ester, manufactured by Toho Chemical Industry Co., Ltd.] 4.5 parts, TSA
-730 R 0.5 part was added and mixed thoroughly, and then 0.8 part of glyphosate / trimesium hydrochloride and 10 parts of isopropyl alcohol were added and dissolved to obtain a liquid preparation.
【0028】実施例13 常水79.9部を溶解タンクに仕込み攪拌しながらニュ
ーコール240R 〔アルキルジサルフェール、日本乳化
剤(株)製〕4.0部、TSA−750R 0.5部を加
えて充分混合したのち、アトラジン0.6部、イソプロ
ピルアルコール15部を加えて溶解させ液剤を得る。Example 13 79.9 parts of ordinary water was charged into a dissolution tank and stirred with Newcol 240 R [alkyldisulfide, manufactured by Nippon Emulsifier Co., Ltd.] 4.0 parts, TSA-750 R 0.5 part. After adding and thoroughly mixing, 0.6 part of atrazine and 15 parts of isopropyl alcohol are added and dissolved to obtain a liquid preparation.
【0029】実施例14 常水43.5部を溶解タンクに仕込み攪拌しながらニュ
ーカルゲンEP−4CR 〔ジアルキルスルホサクシネー
ト・ソーダ塩、竹本油脂(株)製〕20部、イソプロピ
ルアルコール15部およびTSA−730R 1.5部を
加えて充分攪拌したのち、ビアホラス20部を加えて溶
解させ液剤を得る。Example 14 43.5 parts of ordinary water was charged into a dissolution tank and stirred with Newcalgen EP-4C R [dialkylsulfosuccinate soda salt, manufactured by Takemoto Yushi Co., Ltd.] 20 parts, isopropyl alcohol 15 parts and After 1.5 parts of TSA-730 R was added and sufficiently stirred, 20 parts of viaholus was added and dissolved to obtain a liquid agent.
【0030】実施例15 常水54.5部を溶解タンクに仕込み攪拌しながらパラ
コールOPR 〔アルキルフォスフェート、東邦化学工業
(株)製〕20部とTSA−750R 0.5部を加えて
充分混合したのちグリホサート10部とイソプロピルア
ルコール15部を加えて溶解させ液剤を得る。Example 15 54.5 parts of ordinary water was charged into a dissolution tank, and 20 parts of Paracor OP R [alkyl phosphate, manufactured by Toho Chemical Industry Co., Ltd.] and 0.5 part of TSA-750 R were added with stirring. After thoroughly mixing, 10 parts of glyphosate and 15 parts of isopropyl alcohol are added and dissolved to obtain a liquid agent.
【0031】実施例16 常水53.5部を溶解タンクに仕込み攪拌しながらニュ
ーコールSNR 〔アルキルジサルフェート、日本乳化剤
(株)製〕20部とTSA−730R 15部を加えて充
分攪拌したのち、グリホシネート15部とイソプロピル
アルコール10部を加えて溶解させ液剤を得る。Example 16 53.5 parts of ordinary water was charged into a dissolution tank and 20 parts of Newcol SN R [alkyl disulfate, manufactured by Nippon Emulsifier Co., Ltd.] and 15 parts of TSA-730 R were added and stirred sufficiently. After that, 15 parts of glyphosinate and 10 parts of isopropyl alcohol are added and dissolved to obtain a liquid agent.
【0032】参考例1 常水87.0部を溶解タンクに仕込み攪拌しながらニュ
ーカルゲンST−50R 〔ポリオキシアルキレンアリル
フェニルエーテル、竹本油脂(株)製〕2.0部、TS
A−730R 0.2部を加えて充分に攪拌したのちDC
PA0.8部、イソプロピルアルコール10部を加えて
溶解させて液剤を得る。Reference Example 1 87.0 parts of ordinary water was charged into a dissolution tank and stirred with Newcalgen ST-50 R [polyoxyalkylene allyl phenyl ether, manufactured by Takemoto Yushi Co., Ltd.] 2.0 parts TS.
Add 0.2 parts of A-730 R and stir well, then DC
0.8 parts of PA and 10 parts of isopropyl alcohol are added and dissolved to obtain a liquid preparation.
【0033】参考例2 常水87.0部を溶解タンクに仕込み攪拌しながらニュ
ーコール862R 〔ポリオキシエチレンオクチルフェニ
ルエーテル、日本乳化剤(株)製〕2.5部、TSA−
750R 0.1部、イソプロピルアルコール10部を加
えて充分に混合したのち、ビアラホス0.4部を加えて
溶解させて液剤を得る。Reference Example 2 87.0 parts of ordinary water was charged into a dissolution tank and stirred with Newcol 862 R [polyoxyethylene octylphenyl ether, manufactured by Nippon Emulsifier Co., Ltd.] 2.5 parts, TSA-
750 R ( 0.1 part) and isopropyl alcohol (10 parts) are added and mixed thoroughly, and then 0.4 part of bialaphos is added and dissolved to obtain a liquid preparation.
【0034】参考例3 常水873部を溶解タンクに仕込み攪拌しながらソルポ
ール3688R 〔ポリオキシエチレンひまし油、東邦化
学工業(株)製〕2.0部、TSA−730R0.2部
を加えて充分に混合したのち、DCMU0.3部、ター
バシル0.2部、イソプロピルアルコール10部を加え
て溶解させて液剤を得る。Reference Example 3 873 parts of ordinary water was charged into a dissolution tank, 2.0 parts of SORPOL 3688 R [polyoxyethylene castor oil, manufactured by Toho Chemical Industry Co., Ltd.] and 0.2 part of TSA-730 R were added with stirring. And thoroughly mixed, then 0.3 parts of DCMU, 0.2 parts of terbacyl and 10 parts of isopropyl alcohol are added and dissolved to obtain a liquid preparation.
【0035】参考例4 常水96.7部を溶解タンクに仕込み攪拌しながらニュ
ーカルゲンST−50XR 〔ポリオキシアルキレンアリ
ルフェニルエーテル、竹本油脂(株)製〕2.5部、T
SA−730R 0.2部を加えて充分に混合したのち、
グリホサート0.6部を加えて溶解させて液剤を得る。Reference Example 4 96.7 parts of ordinary water was charged into a dissolution tank and stirred with Newcalgen ST-50X R [polyoxyalkylene allyl phenyl ether, manufactured by Takemoto Yushi Co., Ltd.] 2.5 parts, T
After adding 0.2 parts of SA-730 R and mixing thoroughly,
Glyphosate (0.6 part) is added and dissolved to obtain a liquid preparation.
【0036】参考例5 常水86.7部を溶解タンクに仕込み攪拌しながらソル
ポール3539WR 〔ポリオキシエチレンスチリルフェ
ニルエーテル・アルキルアリルスルホネート、東邦化学
工業(株)製〕2.5部、TSA−730R 0.2部、
イソプロピルアルコール10部を加えて充分に混合した
のち、アトラジン0.6部を加えて溶解して液剤を得
た。Reference Example 5 86.7 parts of ordinary water was charged into a dissolution tank and stirred with SOLPOL 3539W R [polyoxyethylene styryl phenyl ether alkylallyl sulfonate, manufactured by Toho Chemical Industry Co., Ltd.] 2.5 parts, TSA- 730 R 0.2 parts,
After adding 10 parts of isopropyl alcohol and thoroughly mixing, 0.6 part of atrazine was added and dissolved to obtain a liquid preparation.
【0037】試験例1 メヒシバ,エノコログサ,カモジグサ,ヌスビトハギを
対象として、それらが草丈20〜30cmに生育した試
験圃場を1区画1m2 に区切り、前記実施例および参考
例で得られた各製剤を各100ml/m2 の量で草の茎
葉全体にポンプ式噴霧器を用いて反復2回均一に散布し
た。雑草の状態は24時間毎に調べた。結果は表1と表
2に、各実施例および参考例の製剤に含有される除草剤
成分と界面活性剤の種類を表3と表4に示す。Test Example 1 Targeting crabgrass, Enocorogosa, Duckweed, and Nupisotohagi, a test field in which they grew to a plant height of 20 to 30 cm was divided into 1 m 2 sections, and each preparation obtained in the above Examples and Reference Examples was divided into An amount of 100 ml / m 2 was sprayed uniformly over the entire foliage of the grass using a pump atomizer twice. Weed condition was checked every 24 hours. The results are shown in Tables 1 and 2, and the types of herbicidal components and surfactants contained in the formulations of Examples and Reference Examples are shown in Tables 3 and 4.
【0038】[0038]
【表1】 注)雑草の状態に対する評価基準 5:100%枯死 4:50%枯死 3:25%枯
死 2:変化あり 1:変化なし[Table 1] Note) Evaluation criteria for weed status 5: 100% death 4: 50% death 3: 25% death 2: Change 1: No change
【0039】[0039]
【表2】 注)雑草の状態に対する評価基準 5:100%枯死 4:50%枯死 3:25%枯
死 2:変化あり 1:変化なし[Table 2] Note) Evaluation criteria for weed status 5: 100% death 4: 50% death 3: 25% death 2: Change 1: No change
【0040】表1と表2から明らかなように、各実施例
の製剤中成績は早いものは24時間後に、遅くても72
時間後には100%枯死の成績を示したが、参考例の製
剤では72時間後においても雑草の状態に変化が多少認
められるかまたは認められない程度の作用しか示さなか
った。As is clear from Tables 1 and 2, the in-formulation results in each Example were 24 hours after the earliest and 72 hours at the latest.
After 100 hours, 100% mortality was shown, but the formulation of Reference Example showed some or no change in the state of weeds even after 72 hours.
【0041】[0041]
【表3】 [Table 3]
【0042】[0042]
【表4】 [Table 4]
【0043】試験例2 本発明に従い陰イオン界面活性剤としてニューカルゲン
EP−4Cを用いた場合と、その代りに陽イオン,非イ
オンまたは両性界面活性剤を用いた製剤および市販の速
効性といわれる製剤と比較した。非イオン界面活性剤と
しては、ニューカルゲンTAKD−3615TR (ポリ
オキシエチレン牛脂アミノエーテル),同TAK300
0SR (四級化ポリオキシエチレンアルキルアミノエー
テル),同TAK89137R (ポリオキシエチレンア
ルキルアリルエーテル)〔以上竹本油脂(株)製〕およ
びレオドールKAOTW−0120R 〔ポリオキシエチ
レンソルビタンモノオレート、花王(株)製〕を用い、
両性界面活性剤としてはアンヒトールKAO24B
R 〔ラウリルベタイン、花王(株)製〕を用いた。Test Example 2 According to the present invention, it is said that Nucargen EP-4C is used as an anionic surfactant, and a preparation using a cationic, nonionic or amphoteric surfactant instead of it and a commercially available fast-acting agent. Compared to formulation. Examples of nonionic surfactants include Newcalgen TAK-3615T R (polyoxyethylene tallow amino ether) and TAK300.
0 S R (quaternized polyoxyethylene alkylamino ether), TAK 89137 R (polyoxyethylene alkyl allyl ether) [all manufactured by Takemoto Yushi Co., Ltd.] and REO DOL KAOTW-0120 R [polyoxyethylene sorbitan monooleate, Kao ( Co., Ltd.]
Amphoteric KAO24B as amphoteric surfactant
R [lauryl betaine, manufactured by Kao Corporation] was used.
【0044】これらの試験製剤は次のように調製した。
すなわち、参考例2において、ビアラホス0.4部、各
種界面活性剤8.5部を用い、また水を全量100部と
なるように用いたほかは同例と同様にして液剤を得た。These test formulations were prepared as follows.
That is, a liquid agent was obtained in the same manner as in Reference Example 2 except that 0.4 part of bialaphos and 8.5 parts of various surfactants were used and the total amount of water was 100 parts.
【0045】上記の各製剤ならびに対照として市販のハ
ービエースの50倍希釈液とパスター液剤について、試
験例1と同様にして除草試験を行い、対象雑草の状況を
経時的に調査して表5の結果を得た。With respect to each of the above-mentioned preparations and a commercially available 50-fold dilution of Herbiace and a paste solution, a weeding test was conducted in the same manner as in Test Example 1, and the situation of the target weeds was investigated over time, and the results in Table 5 were obtained. Got
【0046】[0046]
【表5】 注)雑草の状態に対する判定基準 +++ 100%枯死 ++ 50%枯 + 10%枯
死 ± 葉先枯れ − 変化なし[Table 5] Note) Criteria for weed condition +++ 100% dead + 50% dead + 10% dead ± Leaf tip dead-no change
【0047】[0047]
【発明の効果】本発明によれば人畜に対する安全性が高
、1ないし3日以内に雑草を枯死させることのできる
速効性除草剤が提供される。INDUSTRIAL APPLICABILITY According to the present invention, there is provided a fast-acting herbicide which is highly safe for humans and animals and can kill weeds within 1 to 3 days.
Claims (7)
イオン界面活性剤0.1重量%以上を含有する水性組成
物よりなる直接散布用速効性除草製剤。1. A rapid-acting herbicidal formulation for direct application, which comprises an aqueous composition containing 0.1 to 20% by weight of a herbicide component and 0.1% by weight or more of an anionic surfactant.
%含有される請求項1記載の除草製剤。2. The herbicidal preparation according to claim 1, which contains 0.1 to 20% by weight of an anionic surfactant.
ン界面活性剤が1〜10重量%である請求項1記載の除
草製剤。3. The herbicidal preparation according to claim 1, wherein the herbicidal component is 0.1 to 4% by weight and the anionic surfactant is 1 to 10% by weight.
ダイアジン系,フェノキシ系,カーバメート系,尿素
系,スルホニル尿素系,トリアジン系,ダイアゾール
系,芳香族カルボン酸系,脂肪酸系,ビピリジリウム系
または無機除草剤化合物である請求項1または2記載の
除草製剤。4. The herbicide component is an organic phosphorus type, an acid amide type,
The herbicidal preparation according to claim 1 or 2, which is a diazine-based, phenoxy-based, carbamate-based, urea-based, sulfonylurea-based, triazine-based, diazole-based, aromatic carboxylic acid-based, fatty acid-based, bipyridylium-based or inorganic herbicide compound.
サルフェート系またはホスフェート系陰イオン界面活性
剤である請求項1記載の除草製剤。5. The anionic surfactant is a sulfonate type,
The herbicidal preparation according to claim 1, which is a sulfate or phosphate anionic surfactant.
に対して陰イオン界面活性剤を1重量部以上を含有する
濃厚製剤を水で希釈して調製されたものである請求項1
記載の除草製剤。6. The aqueous composition is prepared by diluting a concentrated preparation containing 1 part by weight or more of an anionic surfactant with 0.1 to 5 parts by weight of a herbicidal component with water. 1
The herbicidal preparation described.
イオン界面活性剤0.1重量%以上を含有する水性組成
物を雑草に直接散布することを特徴とする急速除草方
法。7. A method for rapid weeding, which comprises directly spraying an aqueous composition containing 0.1 to 20% by weight of a herbicide component and 0.1% by weight or more of an anionic surfactant onto weeds.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4355527A JPH0680504A (en) | 1992-07-17 | 1992-12-17 | Herbicidal formulation and herbicidal method |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4-213383 | 1992-07-17 | ||
JP21338392 | 1992-07-17 | ||
JP4355527A JPH0680504A (en) | 1992-07-17 | 1992-12-17 | Herbicidal formulation and herbicidal method |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0680504A true JPH0680504A (en) | 1994-03-22 |
Family
ID=26519775
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4355527A Pending JPH0680504A (en) | 1992-07-17 | 1992-12-17 | Herbicidal formulation and herbicidal method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0680504A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6093681A (en) * | 1996-10-25 | 2000-07-25 | Monsanto Company | Composition and method for treating plants with exogenous chemicals |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63310801A (en) * | 1987-06-10 | 1988-12-19 | ヘキスト・アクチエンゲゼルシヤフト | Liquid agricultural drug composition |
JPH01299205A (en) * | 1988-03-18 | 1989-12-04 | Hoechst Ag | Liquid herbicide |
JPH02295907A (en) * | 1989-05-02 | 1990-12-06 | Rhone Poulenc Agrochim | Liquid concentrated composite based on n- phosphonomethylglycine |
JPH04338308A (en) * | 1991-05-16 | 1992-11-25 | Mitsubishi Petrochem Co Ltd | Herbicide for upland field |
JPH0597601A (en) * | 1991-04-09 | 1993-04-20 | Rhone Poulenc Chim | Plant protection composition |
-
1992
- 1992-12-17 JP JP4355527A patent/JPH0680504A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63310801A (en) * | 1987-06-10 | 1988-12-19 | ヘキスト・アクチエンゲゼルシヤフト | Liquid agricultural drug composition |
JPH01299205A (en) * | 1988-03-18 | 1989-12-04 | Hoechst Ag | Liquid herbicide |
JPH02295907A (en) * | 1989-05-02 | 1990-12-06 | Rhone Poulenc Agrochim | Liquid concentrated composite based on n- phosphonomethylglycine |
JPH0597601A (en) * | 1991-04-09 | 1993-04-20 | Rhone Poulenc Chim | Plant protection composition |
JPH04338308A (en) * | 1991-05-16 | 1992-11-25 | Mitsubishi Petrochem Co Ltd | Herbicide for upland field |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6093681A (en) * | 1996-10-25 | 2000-07-25 | Monsanto Company | Composition and method for treating plants with exogenous chemicals |
US6475953B1 (en) | 1996-10-25 | 2002-11-05 | Monsanto Technology Llc | Composition and method for treating plants with exogenous chemicals |
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