JP4551639B2 - Weeding method by nursery box application and nursery box application preparation - Google Patents
Weeding method by nursery box application and nursery box application preparation Download PDFInfo
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Description
本発明は育苗箱施用による除草方法及び育苗箱施用製剤に関する。より詳しくは、本発明は除草剤組成物を水稲苗移植前に育苗箱に散布し、移植後の本田に発生する雑草を防除する方法、及びその方法に供する製剤に関する。 The present invention relates to a weeding method by application of a seedling box and a preparation for application of a seedling box. More specifically, the present invention relates to a method for spraying a herbicidal composition on a seedling box before transplanting paddy rice seedlings to control weeds generated in the rice field after transplanting, and a preparation used for the method.
移植水稲田の雑草を防除する方法として、水溶解度が15℃で0.5ppm以上の除草剤を含む組成物を移植前の水稲育苗箱に散布して、機械移植することに特徴をもった方法が知られている(特許文献1参照)。
また特定の殺草性有効成分とする粒状除草剤を移植直前の育苗床に均一に散布し、該粒状剤が吸水、膨潤したのち機械移植することを特徴とする移植水稲田の除草方法が知られている(特許文献2参照)。
Also known is a method of weeding transplanted rice fields, characterized in that a granular herbicide as a specific herbicidal active ingredient is uniformly sprayed on a nursery bed immediately before transplanting, and the granular agent absorbs water and swells and then mechanically transplants. (See Patent Document 2).
移植水稲田における雑草防除は、水稲生育上極めて重要であり、また雑草防除の作業効率の上からもいかにして雑草の発生を抑えるかは、水稲生産者にとって極めて重要でありまた関心の高いところである。
従前より行なわれている水稲田雑草の防除手段としては、雑草発生前又は同後の除草剤の本田への散布処理がすべてであった。作業効率の改善、また作業労働の軽減のため、処理薬剤の剤型の新たな開発や、処理薬剤量の単位面積当たりの低減化、また薬剤処理回数の削減、更には薬剤と移植の同時処理等々が行なわれてきているが、これらもすべて本田施用に係わる改良に限られていた。
Weed control in transplanted paddy rice fields is extremely important for the growth of paddy rice, and how to suppress the occurrence of weeds from the viewpoint of the work efficiency of weed control is also extremely important and interesting for paddy rice producers. is there.
Conventionally, as a means of controlling paddy rice weeds, spraying herbicides to Honda before or after weeds emerged was all. In order to improve work efficiency and reduce work labor, new development of treatment drug dosage forms, reduction of the amount of treatment chemicals per unit area, reduction of the number of treatments, and simultaneous treatment of drugs and transplants However, all of these were limited to improvements related to Honda application.
本発明者らは、実用に供せられる新たな雑草防除方法で、且つ作業効率及び作業労働の軽減を格段に向上させる方法を開発すべく検討を重ねた結果、下記に特定される方法及びそのための製剤を見い出し、本発明を完成するに至った。 As a result of repeated studies to develop a new method for controlling weeds that can be put into practical use and to significantly improve work efficiency and reduction of work labor, the present inventors have identified the following method and therefore: Thus, the present invention was completed.
かくして、本発明によれば、見かけ比重1未満で、除草活性化合物及びポリオキシエチレンアルキルエーテル硫酸塩を含有して成り、更に必要に応じ、補助剤を含むところの粒径が約3mm〜約10mmの押し出し粒剤、直径が約6mm〜約20mmで高さが約5mm〜約40mmの発泡錠剤、又は直径が約5mm〜約20mmで長さが約5mm〜約30mmのカプセル剤のいずれか一つの剤を水稲苗の移植前の育苗箱に散布することを特徴とする、移植後の本田雑草の防除方法、並びに見かけ比重1未満で、除草活性化合物とポリオキシエチレンアルキルエーテル硫酸塩を含有し、更に必要に応じ、補助剤を含有して成る粒径が約3mm〜約10mmの押し出し粒剤、直径が約6mm〜約20mmで高さが約5mm〜約40mmの発泡錠剤又は直径が約5mm〜約20mmで長さが約5mm〜約30mmのカプセル剤のいずれか一つの剤である育苗箱施用製剤が提供される。 Thus, according to the present invention, the apparent specific gravity is less than 1, the herbicidal active compound and the polyoxyethylene alkyl ether sulfate are contained, and if necessary, the particle size including the adjuvant is about 3 mm to about 10 mm. Any one of an extruded granule, a foamed tablet having a diameter of about 6 mm to about 20 mm and a height of about 5 mm to about 40 mm, or a capsule having a diameter of about 5 mm to about 20 mm and a length of about 5 mm to about 30 mm A method of controlling Honda weeds after transplanting, characterized by spraying the agent on a seedling box before transplanting rice seedlings, and having an apparent specific gravity of less than 1, containing a herbicidal active compound and polyoxyethylene alkyl ether sulfate, Further, if necessary, an extruded granule having a particle size of about 3 mm to about 10 mm containing an auxiliary agent, an expanded tablet having a diameter of about 6 mm to about 20 mm and a height of about 5 mm to about 40 mm Has nursery box application preparation is any one of the agents of the capsules is about 5mm~ about 30mm diameter length of about 5mm~ about 20mm is provided.
本発明の斯る除草方法及び該製剤を用いると、驚くべきことに、これまで実用的に不可能であった水稲育苗段階での除草活性組成物の苗箱施用(処理)を可能にし、そして本田移植後の雑草発生を抑えることを可能にすると共に水稲に対しての薬害については、許容し得る範囲内に的確に抑えられることができる。 Surprisingly, the use of such a herbicidal method and the preparation of the present invention enables the application (treatment) of a herbicidal active composition in a rice seedling raising stage, which has heretofore been impossible in practice, and It is possible to suppress the occurrence of weeds after transplanting to Honda, and the phytotoxicity to paddy rice can be accurately suppressed within an acceptable range.
下記実施例の結果から明らかなとおり、本発明の方法及び該方法に用いる製剤が除草活性組成物の苗箱施用を可能にし、本田移植後の雑草防除に有効に働き、同時に水稲に対しての薬害を許容できる程度に抑えた。 As is apparent from the results of the following Examples, the method of the present invention and the preparation used in the method enable the herbicidal active composition to be applied to a seedling box, and work effectively for weed control after transplanting to Honda, and at the same time against paddy rice. The chemical damage was suppressed to an acceptable level.
本発明で用いられる除草活性化合物としては、常温で固体のものが好ましく、そして水稲用除草活性化合物であれば、特に限定されるものではないが、好例としては次のものが挙げられる(一般名記載)。
2,4−PA−エチル、ACN、SAP、アジムスルフロン、イマゾスルフロン、インダノファン、エスプロカルブ、エトキシスルフロン、エトベンザニド、オキサジクロメホン、カフェンストロール、クミルロン、クロメプロップ、シクロスルファムロン、シノスルフロン、シハロホップブチル、ジメタメトリン、シメトリン、ジメピペレート、ダイムロン、テニルクロール、ナプロアニリド、ハロスルフロンメチル、ビフェノックス、ピペロホス、ピラゾキシフェン、ピラゾスルフロンエチル、ピラゾレート、ピリブチカルブ、ピリミノバックメチル、フェントラザミド、ブタミホス、プレチラクロール、ブロモブチド、ベンスルフロンメチル、ベンゾビシクロン、ベンゾフェナップ、ベンタゾン、ベンタゾンナトリウム塩、ベンチオカーブ、ペントキサゾン、ベンフレセート、メフェナセット、モリネート及びアニロホス等。
The herbicidal active compound used in the present invention is preferably a solid at room temperature, and is not particularly limited as long as it is a herbicidal active compound for paddy rice, but preferred examples include the following (generic name) Description).
2,4-PA-ethyl, ACN, SAP, azimusulfuron, imazosulfuron, indanophan, esprocarb, ethoxysulfuron, etobenzanide, oxadiclomephone, caffentrol, cumyluron, clomeprop, cyclosulfamuron, sinosulfuron, cihalohopbutyl, dimetamethrin, cimethrin , Dimethylpiperate, dimelon, tenylchlor, naproanilide, halosulfuronmethyl, biphenox, piperophos, pyrazoxifene, pyrazosulfuronethyl, pyrazolate, pyributycarb, pyriminobacmethyl, phentolazamide, butamifos, pretilachlor, bromobutide, bensulfuron methyl, benzobicyclone, Fenap, bentazone, bentazone sodium salt, bench oka Breakfast, Pentoxazone, benfuresate, mefenacet, such as molinate and anilofos.
発泡錠剤に用いる発泡剤としては、炭酸塩と酸との組み合わせで用いることができ、夫々の具体例としては次のものを例示することができる。
炭酸塩: 炭酸ナトリウム、炭酸カリウム、炭酸アンモニウム、重炭酸ナトリウム、重炭酸カリウム、セスキ炭酸ナトリウム等。
酸: クエン酸、コハク酸、マロン酸、シュウ酸、酒石酸、無水マレイン酸、フタル酸、リンゴ酸、クルタル酸、アジピン酸、硫酸アルミニウム等。
As a foaming agent used for an effervescent tablet, it can use by the combination of carbonate and an acid, The following can be illustrated as each specific example.
Carbonate: Sodium carbonate, potassium carbonate, ammonium carbonate, sodium bicarbonate, potassium bicarbonate, sodium sesquicarbonate and the like.
Acid: Citric acid, succinic acid, malonic acid, oxalic acid, tartaric acid, maleic anhydride, phthalic acid, malic acid, kultaric acid, adipic acid, aluminum sulfate, etc.
更に補助剤としては、一般の粒剤に用いるところの固体担体、結合剤、更には本発明の必須構成の界面活性剤に加えて、他の界面活性剤を挙げることができる。そして固体担体としては、鉱物質微粉(例えば、カオリン、クレー、タルク、ベントナイト、珪藻土、炭酸カルシウム、ホワイトカーボン)、塩化カリウムなどの無機塩、又は木粉などの有機物を挙げることができる。結合剤としては、デキストリン、カルボキシメチルセルロース、天然ポリマー(例えば、アラビアゴム等)、合成ポリマー(例えば、ポリビニルアルコール、ポリビニルアセテート等)等を挙げることができる。 Further, examples of the auxiliary agent include solid surfactants and binders used for general granules, and other surfactants in addition to the essential surfactants of the present invention. Examples of the solid carrier include mineral fine powder (for example, kaolin, clay, talc, bentonite, diatomaceous earth, calcium carbonate, white carbon), inorganic salts such as potassium chloride, and organic substances such as wood powder. Examples of the binder include dextrin, carboxymethyl cellulose, natural polymers (for example, gum arabic), synthetic polymers (for example, polyvinyl alcohol, polyvinyl acetate, etc.), and the like.
他の界面活性剤としては、ポリエチレングリコール高級脂肪酸エステル、ポリオキシエチレンアルキルエーテル、ポリオキシエチレンアルキルアリールエーテル、ポリオキシエチレンアリールフェニルエーテル、ソルビタンモノアルキレート、アセチレンアルコール及びアセチレンジオール並びにそれらのアルキレンオキシドの付加物等のノニオン界面活性剤、アルキルアリールスルホン酸塩、ジアルキルスルホン酸塩、リグニンスルホン酸塩、ナフタレンスルホン酸塩及びその縮合物、アルキル硫酸エステル塩、アルキルリン酸エステル塩、アルキルアリール硫酸エステル塩、アルキルアリールリン酸エステル塩、ポリオキシエチレンアルキルエーテル硫酸エステル塩、ポリオキシエチレンアルキルアリールエーテル硫酸エステル塩、ポリオキシエチレンアリールフェニルエーテル硫酸エステル塩、ポリカルボン酸型高分子活性剤、ジアルキルスルホコハク酸エステル塩等のアニオン界面活性剤、更にはシリコーン系界面活性剤、フッ素系界面活性剤等々を挙げることができる。 Other surfactants include polyethylene glycol higher fatty acid esters, polyoxyethylene alkyl ethers, polyoxyethylene alkyl aryl ethers, polyoxyethylene aryl phenyl ethers, sorbitan monoalkylates, acetylene alcohols and acetylenic diols and their alkylene oxides. Nonionic surfactants such as adducts, alkylaryl sulfonates, dialkyl sulfonates, lignin sulfonates, naphthalene sulfonates and their condensates, alkyl sulfates, alkyl phosphates, alkylaryl sulfates , Alkylaryl phosphate ester salt, polyoxyethylene alkyl ether sulfate ester salt, polyoxyethylene alkyl aryl ether sulfate ester salt, Carboxymethyl ethylene aryl phenyl ether sulfuric acid ester salts, polycarboxylic acid type polymer, an anionic surfactant such as a dialkyl sulfosuccinate salt, more can be mentioned silicone-based surfactants, and so fluorosurfactant.
本発明で用いる粒剤及び発泡錠剤は、好ましくは本田の田面水において、浮遊性を有することにより、一層の効果を現わすことができる。
このような浮遊性を持たせるために、本発明で用いる粒剤及び発泡錠剤は、発泡性パーライト、発泡性シラス、プラスチック中空体等を含有することができる。
The granule and the effervescent tablet used in the present invention can exhibit a further effect by having floatability, preferably in the rice field water of Honda.
In order to provide such floating properties, the granules and effervescent tablets used in the present invention can contain effervescent pearlite, effervescent shirasu, plastic hollow bodies, and the like.
本発明で用いる押し出し粒剤、発泡錠剤又はカプセル剤における各成分の配合割合は、実質的に広い範囲にわたって変えることができる。そして一般には、製剤中の重量%で、除草活性化合物を約1〜約20重量%、好ましくは約3〜約15重量%、ポリオキシエチレンアルキルエーテル硫酸塩を約2〜約7重量%、好ましくは約3〜約5重量%、そしてその他の補助剤を残分量として配合することができる。 The blending ratio of each component in the extruded granule, effervescent tablet or capsule used in the present invention can vary over a substantially wide range. And generally from about 1 to about 20% by weight of the herbicidal active compound, preferably from about 3 to about 15% by weight, and from about 2 to about 7% by weight of polyoxyethylene alkyl ether sulfate, preferably by weight% in the formulation. From about 3 to about 5% by weight, and other adjuncts can be included in the balance.
本発明で用いる押し出し粒剤は、粒径が約3mm〜約10mm、好ましくは約3mm〜約9mmの範囲内であり、同じく発泡錠剤は、直径が約6mm〜約20mm、好ましくは約6mm〜約9mmで、高さが約5mm〜約40mm、好ましくは約10mm〜約15mmであり、また同じくカプセル剤は、直径が約5mm〜約20mm、好ましくは約6mm〜約15mmで、長さが約5mm〜約30mm、好ましくは約7mm〜約25mmであるものを挙げることができる。 The extruded granules used in the present invention have a particle size in the range of about 3 mm to about 10 mm, preferably about 3 mm to about 9 mm, and the effervescent tablet also has a diameter of about 6 mm to about 20 mm, preferably about 6 mm to about 9 mm. 9 mm, the height is about 5 mm to about 40 mm, preferably about 10 mm to about 15 mm, and the capsule is also about 5 mm to about 20 mm in diameter, preferably about 6 mm to about 15 mm, and about 5 mm in length. To about 30 mm, preferably about 7 mm to about 25 mm.
本発明で用いる押し出し粒剤は、通常の押し出し造粒法によって調製することができる。具体的には、例えば、以上に述べた構成成分を水と共に混練した後、押し出し造粒機を用いて造粒することによって製造することができる。練合の際用いる水の量は厳密に制限されるものではないが、全重量に対して、通常5〜50%、好ましくは15〜35%の範囲内とすることができる。
また、発泡錠剤は通常の打錠機を用いて調製することができる。
The extruded granule used in the present invention can be prepared by an ordinary extrusion granulation method. Specifically, for example, the components described above can be kneaded with water and then granulated using an extrusion granulator. The amount of water used in the kneading is not strictly limited, but can be usually 5 to 50%, preferably 15 to 35%, based on the total weight.
Effervescent tablets can be prepared using a normal tableting machine.
カプセル剤は、ごく一般に用いられるところのゼラチンを主として基剤としてなるカプセル中に本発明に従う構成成分から成る顆粒状、細粒状又は粉末状の調製物を充填することにより容易に得ることができる。
カプセル剤に用いる顆粒状又は細粒状の調製物は、上記押し出し造粒法に従って得ることができ、また粉末状の調製物は、通常の農薬の粉剤を調製する方法に従って得られる。
Capsules can be easily obtained by filling granular, fine or powdery preparations comprising the constituents according to the invention into capsules based mainly on gelatin, which is very commonly used.
The granular or fine-grained preparation used for the capsule can be obtained according to the above-mentioned extrusion granulation method, and the powdery preparation can be obtained according to the usual method for preparing an agrochemical powder.
以下、実施例を挙げて本発明を更に具体的に説明するが、本発明はこれらに限定されるものではない。なお、実施例中、%は重量%を示す。 EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples, but the present invention is not limited to these examples. In the examples,% indicates% by weight.
(発明製剤例1)
フェントラザミド原末(70.8%) 3.05%
ベンスルフロンメチル原末(9.9%) 5.66%
ダイムロン原末(84.8%) 5.73%
カルボキシメチルセルロースのナトリウム塩 20.0%
ポリカルボン酸型陰イオン界面活性剤 2.0%
リグニンスルホン酸のナトリウム塩 2.0%
ポリオキシエチレンアルキルエーテル硫酸塩 5.0%
木粉 残分
以上の粉末を混合機を用いて均一に混合した後、水35重量%を加えて混練し、ついで口径3.0mmのスクリーンを装着した押し出し造粒機を用いて造粒する。乾燥後、目開きが2.0mmから5.6mmの篩を用いて整粒し、押し出し粒剤を得る。
(Invention Formulation Example 1)
Fentrazamide raw powder (70.8%) 3.05%
Bensulfuron methyl bulk powder (9.9%) 5.66%
Daimron bulk powder (84.8%) 5.73%
Sodium salt of carboxymethyl cellulose 20.0%
Polycarboxylic acid type anionic surfactant 2.0%
Sodium salt of lignin sulfonic acid 2.0%
Polyoxyethylene alkyl ether sulfate 5.0%
Wood powder residue After the above powder is uniformly mixed using a mixer, 35% by weight of water is added and kneaded, and then granulated using an extrusion granulator equipped with a screen having a diameter of 3.0 mm. After drying, the particles are sized using a sieve having an opening of 2.0 mm to 5.6 mm to obtain extruded granules.
(発明製剤例2)
上記実施例1と同じ構成の粉末を同様に混練し、口径5.0mmのスクリーンで押し出し造粒する。
(Invention Formulation Example 2)
A powder having the same structure as in Example 1 is kneaded in the same manner and extruded and granulated with a screen having a diameter of 5.0 mm.
(発明製剤例3)
フェントラザミド原末(70.8%) 3.05%
ベンスルフロンメチル原末(9.9%) 5.66%
ダイムロン原末(84.8%) 5.73%
ブラスチック中空体 1.5%
ジアルキルスルホコハク酸エステルナトリウム塩 2.0%
デキストリン 2.0%
ポリオキシエチレンアルキルエーテル硫酸塩 3.0%
塩化カリウム 残分
上記実施例2と同様にして、径5.0mmの粒剤を得る。
(Invention Formulation Example 3)
Fentrazamide raw powder (70.8%) 3.05%
Bensulfuron methyl bulk powder (9.9%) 5.66%
Daimron bulk powder (84.8%) 5.73%
Plastic hollow body 1.5%
Dialkylsulfosuccinate sodium salt 2.0%
Dextrin 2.0%
Polyoxyethylene alkyl ether sulfate 3.0%
Potassium chloride residue Granules having a diameter of 5.0 mm are obtained in the same manner as in Example 2 above.
(発明製剤例4)
フェントラザミド原末(70.8%) 3.05%
ベンスルフロンメチル原末(9.9%) 5.66%
ダイムロン原末(84.8%) 5.73%
カルボキシメチルセルロースのナトリウム塩 5.0%
ジアルキルスルホコハク酸エステルナトリウム塩 2.0%
タルク 5.0%
ポリオキシエチレンアルキルエーテル硫酸塩 3.0%
クエン酸 22.62%
炭酸水素ナトリウム 29.7%
木粉 残分
以上の粉末を混合機を用いて均一に混合した後、単発打錠機を用いて打錠し、直径9mmの発泡錠剤を得る。
(Invention Formulation Example 4)
Fentrazamide raw powder (70.8%) 3.05%
Bensulfuron methyl bulk powder (9.9%) 5.66%
Daimron bulk powder (84.8%) 5.73%
Sodium salt of carboxymethyl cellulose 5.0%
Dialkylsulfosuccinate sodium salt 2.0%
Talc 5.0%
Polyoxyethylene alkyl ether sulfate 3.0%
Citric acid 22.62%
Sodium bicarbonate 29.7%
Wood powder residue After the above powder is uniformly mixed using a mixer, it is tableted using a single tableting machine to obtain an expanded tablet having a diameter of 9 mm.
(発明製剤例5)
フェントラザミド原末(70.8%) 3.05%
ベンスルフロンメチル原末(9.9%) 5.66%
ダイムロン原末(84.8%) 5.73%
カルボキシメチルセルロースのナトリウム塩 20.0%
ポリカルボン酸型陰イオン界面活性剤 2.0%
リグニンスルホン酸のナトリウム塩 2.0%
ポリオキシエチレンアルキルエーテル硫酸塩 5.0%
木粉 残分
以上の粉末を混合機を用いて均一に混合した後、水20重量%を加えて混練し、ついで口径0.5mmのスクリーンを装着した押し出し造粒機を用いて造粒する。乾燥後、目開きが0.2mmから1.0mmの篩を用いて整粒し、顆粒状物を得る。
この顆粒状のものを、直径6mm、長さ15mmのゼラチンカプセルに充填し、カプセル剤を得る。
(Invention Formulation Example 5)
Fentrazamide raw powder (70.8%) 3.05%
Bensulfuron methyl bulk powder (9.9%) 5.66%
Daimron bulk powder (84.8%) 5.73%
Sodium salt of carboxymethyl cellulose 20.0%
Polycarboxylic acid type anionic surfactant 2.0%
Sodium salt of lignin sulfonic acid 2.0%
Polyoxyethylene alkyl ether sulfate 5.0%
Wood powder residue After the above powder is uniformly mixed using a mixer, 20% by weight of water is added and kneaded, and then granulated using an extrusion granulator equipped with a screen having a diameter of 0.5 mm. After drying, the granules are sized using a sieve having an opening of 0.2 mm to 1.0 mm to obtain a granular product.
This granular product is filled into a gelatin capsule having a diameter of 6 mm and a length of 15 mm to obtain a capsule.
比較製剤例
フェントラザミド原末(70.8%) 3.05%
ベンスルフロンメチル原末(9.9%) 5.66%
ダイムロン原末(84.8%) 5.73%
ポリカルボン酸型陰イオン界面活性剤 1.0%
ジアルキルスルホコハク酸エステルナトリウム塩 0.2%
酵素変性デキストリン 1.0%
ポリオキシアルキレンアリールフェニールエーテル
硫酸塩 3.5%
トリポリリン酸ナトリウム 2.0%
ベントナイト 30.0%
炭酸カルシウム 残分
上記粉末を実施例1と同様にして、0.8mmのスクリーンで押し出し造粒する。
Comparative formulation example Fentrazamide powder (70.8%) 3.05%
Bensulfuron methyl bulk powder (9.9%) 5.66%
Daimron bulk powder (84.8%) 5.73%
Polycarboxylic acid type anionic surfactant 1.0%
Dialkylsulfosuccinate sodium salt 0.2%
Enzyme-modified dextrin 1.0%
Polyoxyalkylene aryl phenyl ether sulfate 3.5%
Sodium tripolyphosphate 2.0%
Bentonite 30.0%
Calcium carbonate residue The powder is extruded and granulated in the same manner as in Example 1 using a 0.8 mm screen.
試験例 除草並びに薬害試験
供試製剤:
発明製剤1(=前記実施例1) 粒径3mm粒剤
発明製剤2(=前記実施例4) 発泡錠剤
比較製剤(=前記比較製剤例) 粒径0.8mm粒剤
方法:
田植当日移植前、育苗箱に1箱あたり製剤50gを処理した(10アールあたり20箱)。処理された稚苗は、湛水約1cmの本田に機械移植された。
田植後10日間隔で40日まで肉眼評価した。薬効薬害の評価は、0が無影響、100%が完全枯死を意味する。水稲薬害10%以下:許容範囲。
結果:
───────────────────────────────────
タイヌビ タマガ コナギ 広葉 ホタル 水稲薬 水稲欠
エ効果 ヤツリ イ 害 株率
───────────────────────────────────
発明製剤1 100 100 100 97 90 10 0
箱処理
───────────────────────────────────
発明製剤2 98 100 100 97 90 9 1
箱処理
───────────────────────────────────
比較製剤 100 100 100 97 100 95 40
箱処理
───────────────────────────────────
比較製剤 100 100 100 98 100 2 0
田植同時
───────────────────────────────────
Test example Herbicidal and phytotoxicity test formulation:
Invention formulation 1 (= Example 1 above) Particle size 3 mm granule Invention formulation 2 (= Example 4 above) Effervescent tablet Comparative formulation (= Comparative formulation example) Particle size 0.8 mm granule Method:
Prior to transplanting on the day of rice transplantation, 50 g of the preparation per box was treated in a seedling box (20 boxes per 10 ares). The treated seedlings were mechanically transplanted to Honda, which was about 1 cm in water.
Macroscopic evaluation was performed up to 40 days at 10-day intervals after rice transplanting. In the evaluation of medicinal effects, 0 means no effect and 100% means complete death. Paddy rice chemical damage 10% or less: allowable range.
result:
───────────────────────────────────
Tainubi Tamaga Konagi Broadleaf Firefly Paddy Rice Missing Rice
Effect of effect File damage rate
───────────────────────────────────
Invention formulation 1 100 100 100 97 90 10 0
Box processing
───────────────────────────────────
Invention formulation 2 98 100 100 97 90 9 1
Box processing
───────────────────────────────────
Comparative formulation 100 100 100 97 100 95 40
Box processing
───────────────────────────────────
Comparative preparation 100 100 100 98 100 2 0
Rice planting simultaneously
───────────────────────────────────
Claims (6)
A seedling box having an apparent specific gravity of less than 1, containing a herbicidal active compound and polyoxyethylene alkyl ether sulfate, and further containing an adjuvant and having a diameter of 6 mm to 20 mm and a length of 5 mm to 30 mm. Application formulation.
Herbicidal active compounds are 2,4-PA-ethyl, ACN, SAP, azimusulfuron, imazosulfuron, indanophan, eprocarb, ethoxysulfuron, etobenzanide, oxadichromemephone, kafenstrol, cumyllon, clomeprop, cyclosulfamuron, sinosulfuron, cihalohop Butyl, dimetamethrin, cimethrin, dimepiperate, dimrone, tenylchlor, naproanilide, halosulfuronmethyl, biphenox, piperophos, pyrazoxifene, pyrazosulfuronethyl, pyrazolate, pyributicarb, pyriminobacmethyl, phentolazamide, butamiphos, pretilacrol, bromobutyrode Benzobicyclon, benzophenap, bentazone, bentazon natri Unsalted, benthiocarb, pentoxazone, benfuresate, mefenacet, nursery box application formulation according to claim 3, 4 or 5 is at least one selected from the group consisting of molinate and anilofos.
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