JP2006282643A - Insect pest control solution for heating transpiration containing pyrethrum extract as effective component and method of insect pest control - Google Patents

Insect pest control solution for heating transpiration containing pyrethrum extract as effective component and method of insect pest control Download PDF

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JP2006282643A
JP2006282643A JP2005108595A JP2005108595A JP2006282643A JP 2006282643 A JP2006282643 A JP 2006282643A JP 2005108595 A JP2005108595 A JP 2005108595A JP 2005108595 A JP2005108595 A JP 2005108595A JP 2006282643 A JP2006282643 A JP 2006282643A
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pest control
insecticidal
solution
insect pest
heating
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Keisuke Watanabe
渡辺敬介
Kazumi Sugiki
杉木和美
Masato Mizutani
水谷理人
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Sumika Life Tech Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide an insecticidal solution stably expressing insect pest control effects for a long time by heating by installing the same in biotope of the insect pests, and an insecticidal method. <P>SOLUTION: The insecticidal solution is prepared by dissolving a pyrethrum extract and a phenol-based antioxidant in a straight chain hydrocarbon or a branched chain hydrocarbon having 200-300°C temperature of 50% off. The insecticidal solution is stably transpired by soaking a part of a porous liquid absorbent wick in the insecticidal solution and heating the unsoaked part of the wick while allowing the insecticidal solution to be absorbed into the wick. The insecticidal solution can decrease the used amount of the effective components from the standpoint of its effect without using materials suspicious to have influences to human bodies and the environment. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

本発明は、天然に存在する殺虫成分であるジョチュウギクエキスを有効成分とする害虫防除液を使用し、これを加熱して有効成分を効率的に蒸散させて人体や環境への負荷を少なくした条件で人体に有害なハエ、蚊、ゴキブリなどの害虫を駆除する方法を提供することである。
The present invention uses a pest control solution comprising a natural wormwood extract, which is a naturally occurring insecticidal component, as an active ingredient, and heats it to efficiently evaporate the active ingredient, thereby reducing the burden on the human body and the environment. It is to provide a method for controlling flies, mosquitoes, cockroaches and other pests that are harmful to the human body under these conditions.

本発明の有効成分の一つであるジョチュウギクエキスを含有する殺虫剤としては下記文献のハチ駆除用でエアゾールが知られている。また、衛生害虫駆除剤としては、商品名「インセクトサイド,ピレトリン」(仲本エンタープライズ(株))があるが、この製品には、殺虫効力を増強させる共力剤であるピペロニルブトキサイド(PBO)が有効成分の2.3倍も含まれており、この共力剤の削減が求められている。またピレスロイド系薬剤であるプラレトリンを炭化水素系溶剤に溶解させ、これを多孔質吸液芯の一部を浸漬して、該芯に害虫防除液を吸わせてながら、該芯の非浸漬部分を加熱することにより吸液された害虫防除液を大気中に蒸散させて害虫を駆除する製品も市販されている。   As an insecticide containing the licorice extract which is one of the active ingredients of the present invention, an aerosol is known for bee control in the following literature. In addition, as a sanitary pest control agent, there is a trade name “Insectside, Piretrin” (Nakamoto Enterprise Co., Ltd.), but this product contains piperonyl butoxide (PBO), a synergist that enhances insecticidal efficacy. ) Is 2.3 times as much as the active ingredient, and there is a need to reduce this synergist. Further, pyrethrin, which is a pyrethroid, is dissolved in a hydrocarbon solvent, and a portion of the porous liquid absorbent core is immersed in the pestroid so that the pest control liquid is sucked into the core while the non-immersed portion of the core is absorbed. A product that exterminates pests by evaporating the pest control liquid absorbed by heating into the atmosphere is also commercially available.

特開2004−269406号公報JP 2004-269406 A

本発明は、天然に存在する殺虫成分であるジョチュウギクエキスを有効成分として溶解した害虫防除液の加熱蒸散を長期間安定して行うことを可能とし、これにより安定した害虫防除効果を長期間持続させることが可能な加熱蒸散用害虫防除液を提供することにある。
The present invention makes it possible to stably carry out heat transpiration of a pest control solution obtained by dissolving a natural wormwood extract, which is a naturally occurring insecticidal component, as an active ingredient, thereby providing a stable pest control effect over a long period of time. The object is to provide a pest control solution for heat evaporation that can be sustained.

本発明者らはジョチュウギクエキスを有効成分として溶解させた加熱蒸散害虫防除液が長期間に渡って効果を発揮する殺虫方法について検討を重ねた結果、本発明を完成した。   The inventors of the present invention have completed the present invention as a result of repeated studies on an insecticidal method in which a heat-transpirating insect pest control solution in which a mulberry extract is dissolved as an active ingredient is effective over a long period of time.

本発明は以下のものである。
1. 50%留出温度が200〜300℃の直鎖ないし分岐鎖状飽和炭化水素(以下、(a)成分と記す。)を60〜99.99重量%、ジョチュウギクエキス(以下、(b)成分と記す。)を0.1〜10重量%およびフェノール系酸化防止剤(以下、(c)成分と記す。)を0.01〜10重量%含有させた加熱蒸散用害虫防除液(以下、本殺虫液)。
2. 本殺虫液中に、多孔質吸液芯の一部を浸漬して、該芯に害虫防除液を吸わせながら、該芯の非浸漬部分を加熱することにより吸液された害虫防除液を大気中に安定的に蒸散させて、人体や環境への影響を疑われている資材を使用せず、効力面でも有効成分の使用量を減らした害虫を駆除する方法
3. 加熱温度が150〜280℃である1.に記載の殺虫方法
The present invention is as follows.
1. 60 to 99.99% by weight of straight or branched saturated hydrocarbon (hereinafter referred to as component (a)) having a 50% distillation temperature of 200 to 300 ° C., chrysanthemum extract (hereinafter referred to as (b) Pest control solution for heat evaporation (hereinafter referred to as “component”) containing 0.1 to 10 wt% and phenolic antioxidant (hereinafter referred to as “component (c)”) 0.01 to 10 wt%. This insecticide).
2. In this insecticide, a part of the porous absorbent core is dipped, and the pest control liquid absorbed by heating the non-immersed part of the core is sucked into the atmosphere while sucking the pest control liquid into the core. 2. A method of exterminating pests that have been stably evaporated and do not use materials that are suspected of affecting the human body or the environment, and have reduced the amount of active ingredients used in terms of efficacy. 1. Heating temperature is 150-280 ° C. Insecticidal method described in

天然に存在する殺虫成分であるジョチュウギクエキスを、50%留出温度が200〜300℃の直鎖状飽和炭化水素に、フェノール系酸化防止剤とともに溶解させた害虫防除液を調製し、これを加熱して有効成分を効率的に蒸散させることにより、人体や環境への負荷を少なくした条件でハエ、蚊、ゴキブリなどの害虫を駆除することができるようになった。   A pest control solution is prepared by dissolving a cypress extract, a naturally occurring insecticidal component, in a linear saturated hydrocarbon having a 50% distillation temperature of 200 to 300 ° C. together with a phenolic antioxidant. By heating the water and efficiently evaporating the active ingredients, it has become possible to control pests such as flies, mosquitoes and cockroaches under conditions that reduce the burden on the human body and the environment.

本発明に使用されるジョチュウギクエキスは、天然に存在する植物であるジョチュウギクから抽出されたものであり、殺虫有効成分を6種含有しているものである。前記殺虫有効成分とは、表1に記載した6成分であり、これらを合わせて総ピレトリンといわれている。本発明に使用されるジョチュウギクエキスに含まれる前記総ピレトリン量は、10〜90重量%、好ましくは20〜80重量%のものが使用される。
なお本殺虫液に溶解されるジョチュウギクエキスの量は、本殺虫液中の0.1〜10重量%、好ましくは0.2〜8重量%である。
The Oyster extract used in the present invention is extracted from Oyster, which is a naturally occurring plant, and contains six insecticidal active ingredients. The insecticidal active ingredients are the six ingredients listed in Table 1, and are collectively referred to as total pyrethrin. The total amount of pyrethrin contained in the licorice extract used in the present invention is 10 to 90% by weight, preferably 20 to 80% by weight.
It should be noted that the amount of chrysanthemum extract dissolved in this insecticide is 0.1 to 10% by weight, preferably 0.2 to 8% by weight in this insecticide.

Figure 2006282643
Figure 2006282643

本発明において50%留出温度とはJIS K 2254に記載の方法により常圧蒸留を行った場合に得られる溶媒種、その構成比率等により決まる固有の値である。   In the present invention, the 50% distillation temperature is a specific value determined by the solvent species obtained when atmospheric distillation is performed by the method described in JIS K 2254, the constituent ratio, and the like.

本発明において用いられる(a)成分としてはドデカン(50%留出温度 約216℃)、トリデカン(50%留出温度 約235℃)、テトラデカン(50%留出温度 約253℃)、ペンタデカン(50%留出温度 約270℃)等のノルマルパラフィン、ノルマルパラフィン系混合物の溶剤であるノルパー13(エクソンモービル化学 50%留出温度 約231℃)、ノルパー15(エクソンモービル化学 50%留出温度 約261℃)、0号ソルベントM(日本石油化学 50%留出温度 約226℃)0号ソルベントH(日本石油化学 50%留出温度 約250℃)、ネオチオゾール(中央化成50%留出温度 約220℃)、IPソルンベント2028(出光石油化学、50%留出温度 約233℃、アイソパーM(エクソンモービル、50%留出温度 約234℃)、メルベイユ40(昭和石油、50%留出温度 約229℃)等があげられ、これらを単独または2種類以上混合して使用することができる。
As the component (a) used in the present invention, dodecane (50% distillation temperature about 216 ° C.), tridecane (50% distillation temperature about 235 ° C.), tetradecane (50% distillation temperature about 253 ° C.), pentadecane (50 Norpar 13 (ExxonMobil chemistry 50% distillation temperature 231 ° C), Norpar 15 (ExxonMobil chemistry 50% distillation temperature 261) No. 0 Solvent M (Nippon Petrochemical 50% distillation temperature approx. 226 ° C) No. 0 Solvent H (Nippon Petrochemical 50% distillation temperature approx. 250 ° C), Neothiozol (Central Chemical 50% distillation temperature approx. 220 ° C) ), IP solvent 2028 (Idemitsu Petrochemical, 50% distillation temperature about 233 ° C, Isopar M (Exxon Mobil, 50% distillation temperature) About 234 ° C.), Merveille 40 (Showa oil, 50% distillation temperature about 229 ° C.) and the like, can be used as a mixture thereof alone, or two or more kinds.

フェノール系酸化防止剤としては2,6−ジーt−ブチルー4−メチルフェノール(BHT)、2−tーブチルヒドロキシアニソール(BHA)、4,4‘−ブチリデンビス(3−メチルー6−t−ブチルフェノール)、3,9−ビス[2−[3−(3−t−ブチルー4−ヒドロキシー5−メチルフェニル)−プロピオニ オロキシ]−1,1−ジメチル]−2,4,8,10−テトラオキザスピロ[5・5]ウンデカン等が挙げられる。 2,6-di-t-butyl-4-methylphenol (BHT), 2-tert-butylhydroxyanisole (BHA), 4,4′-butylidenebis (3-methyl-6-tert-butylphenol) as phenolic antioxidants 3,9-bis [2- [3- (3-t-butyl-4-hydroxy-5-methylphenyl) -propionioxy] -1,1-dimethyl] -2,4,8,10-tetraoxaspiro [5.5] Undecane and the like.

本殺虫液には必要に応じて他の溶剤、パラヒドロキシ安息香酸エステル系の安定化剤、香料、ヒノキチオール、3―メチルー4−イソプロピルフェノール、チモールまたはカルバクロルのような防カビ剤、他のピレスロイド系殺虫剤、害虫忌避剤、メタクリル酸ラウリル等の消臭剤等が含有されていてもよい。   This insecticide contains other solvents, parahydroxybenzoic acid ester stabilizers, fragrances, hinokitiol, 3-methyl-4-isopropylphenol, fungicides such as thymol or carbchlor, and other pyrethroids as necessary. An insecticide, a pest repellent, a deodorant such as lauryl methacrylate, and the like may be contained.

本殺虫液に用いることができる他の溶剤としてはメタノール、エタノール、イソプロピルアルコール、アミルアルコール等の1価アルコール、グリセリン、ブチルジグリコール、エチレングリコール、プロピレングリコール等の2価アルコール、エチレングリコールモノメチルエーテル、エチレングリコールモノエチルエーテル、エチレングリコールモノブチルエーテル、ジエチレングリコールモノメチルエーテル、ジエチレングリコールモノエチルエーテル、ジエチレングリコールモノブチルエーテル、プロピレングリコールモノメチルエーテル、プロピレングリコールモノエチルエーテル、プロピレングリコールモノブチルエーテル等のグリコールアルキルエーテル系界面活性剤が挙げられる。   Other solvents that can be used in this insecticide include monohydric alcohols such as methanol, ethanol, isopropyl alcohol, and amyl alcohol, dihydric alcohols such as glycerin, butyl diglycol, ethylene glycol, and propylene glycol, ethylene glycol monomethyl ether, Examples include glycol alkyl ether surfactants such as ethylene glycol monoethyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, propylene glycol monomethyl ether, propylene glycol monoethyl ether, and propylene glycol monobutyl ether. It is done.

香料としては、例えばペパーミント、ハッカ、ヒノキ、ヒバ、パイン、ラベンダー、パチョリ、ユーカリ、シトロネラ、ライム、タイム、ヒソップ、ローズマリー、ティツリー、マヌカ、イランイラン、クローブ、ベイ、セージ等の植物精油、サリチル酸メチル、フェノキシエタノール、リナロール、シネオール、シトロネオール、シトロネラール、オイゲノール、メントール、メントン等の天然香料、及び合成香料が挙げられる。本発明の加熱蒸散用消臭液中には、香料が本発明の加熱蒸散用消臭液全量に対して、通常5重量%以下の量が含有される。   Examples of flavors include peppermint, mint, cypress, hiba, pine, lavender, patchouli, eucalyptus, citronella, lime, thyme, hyssop, rosemary, tea tree, manuka, ylang ylang, clove, bay, sage and other plant essential oils, salicylic acid Examples include natural fragrances such as methyl, phenoxyethanol, linalool, cineol, citronole, citronellal, eugenol, menthol and menthone, and synthetic fragrances. In the deodorizing liquid for heat evaporation of the present invention, the fragrance is usually contained in an amount of 5% by weight or less based on the total amount of the deodorizing liquid for heat evaporation of the present invention.

混合しうる他のピレスロイド系殺虫剤としては、例えば2−メチル−3−アリル−4−オキソ−2−シクロペンテン−1−イル 3−(2−メチル−1−プロペニル)−2,2−ジメチルシクロプロパンカルボキシラート、2−メチル−3−プロパルギル−4−オキソ−2−シクロペンテン−1−イル 3−(2−メチル−1−プロペニル)−2,2−ジメチルシクロプロパンカルボキシラート、1−エチニル−2−メチル−2−ペンテニル 3−(2−メチル−1−プロペニル)−2,2−ジメチルシクロプロパンカルボキシラート、5−プロパルギル−2−フルフリル 3−(2−メチル−1−プロペニル)−2,2−ジメチルシクロプロパンカルボキシラート、3−(2−クロロ−2−フルオロビニル)−2,2−ジメチルシクロプロパン−1−カルボキシラート、1−エチニル−2−メチル−2−ペンテニル 3−(2−クロロ−2−フルオロビニル)−2,2−ジメチルシクロプロパン−1−カルボキシラート、2,3,5,6−テトラフルオロ−4−メチルベンジル 3−(2,2−ジクロロビニル)−2,2−ジメチルシクロプロパンカルボキシラート、2,3,5,6−テトラフルオロ−4−メチルベンジル 3−(2−メチル−1−プロペニル)−2,2−ジメチルシクロプロパンカルボキシラート、2,3,5,6−テトラフルオロ−4−メチルベンジル 3−(1−プロペニル)−2,2−ジメチルシクロプロパンカルボキシラート、2−メチル−3−アリル−4−オキソ−2−シクロペンテン−1−イル 2,2,3,3−テトラメチルシクロプロパンカルボキシラート、2,3,5,6−テトラフルオロ−4−メトキシルベンジル 3−(2,2−ジクロロビニル)−2,2−ジメチルシクロプロパンカルボキシラート、2,3,5,6−テトラフルオロ−4−メトキシルベンジル 3−(1−プロペニル)−2,2−ジメチルシクロプロパンカルボキシラート、2,3,5,6−テトラフルオロベンジル 3−(2,2−ジクロロビニル)−2,2−ジメチルシクロプロパンカルボキシラート、2,3,5,6−テトラフルオロ−4−メトキシルベンジル 3−(2−メチル−1−プロペニル)−2,2−ジメチルシクロプロパンカルボキシラート、2,3,5,6−テトラフルオロ−4−メトキシベンジル 3−メトキシイミノメチル−2,2−ジメチルシクロプロパンカルボキシラート等のピレスロイド系殺虫性化合物が挙げられる。これらの化合物には、シクロプロパン環、及び二重結合に基づく異性体が存在する場合があるが、この場合は活性な任意の異性体を使用することができる。   Other pyrethroid insecticides that can be mixed include, for example, 2-methyl-3-allyl-4-oxo-2-cyclopenten-1-yl 3- (2-methyl-1-propenyl) -2,2-dimethylcyclo Propanecarboxylate, 2-methyl-3-propargyl-4-oxo-2-cyclopenten-1-yl 3- (2-methyl-1-propenyl) -2,2-dimethylcyclopropanecarboxylate, 1-ethynyl-2 -Methyl-2-pentenyl 3- (2-methyl-1-propenyl) -2,2-dimethylcyclopropanecarboxylate, 5-propargyl-2-furfuryl 3- (2-methyl-1-propenyl) -2,2 -Dimethylcyclopropanecarboxylate, 3- (2-chloro-2-fluorovinyl) -2,2-dimethylcycloprop -1-carboxylate, 1-ethynyl-2-methyl-2-pentenyl 3- (2-chloro-2-fluorovinyl) -2,2-dimethylcyclopropane-1-carboxylate, 2,3,5,6 -Tetrafluoro-4-methylbenzyl 3- (2,2-dichlorovinyl) -2,2-dimethylcyclopropanecarboxylate, 2,3,5,6-tetrafluoro-4-methylbenzyl 3- (2-methyl) -1-propenyl) -2,2-dimethylcyclopropanecarboxylate, 2,3,5,6-tetrafluoro-4-methylbenzyl 3- (1-propenyl) -2,2-dimethylcyclopropanecarboxylate, 2 -Methyl-3-allyl-4-oxo-2-cyclopenten-1-yl 2,2,3,3-tetramethylcyclopropanecarboxyl 2,3,5,6-tetrafluoro-4-methoxylbenzyl 3- (2,2-dichlorovinyl) -2,2-dimethylcyclopropanecarboxylate, 2,3,5,6-tetrafluoro-4 -Methoxylbenzyl 3- (1-propenyl) -2,2-dimethylcyclopropanecarboxylate, 2,3,5,6-tetrafluorobenzyl 3- (2,2-dichlorovinyl) -2,2-dimethylcyclopropane Carboxylate, 2,3,5,6-tetrafluoro-4-methoxylbenzyl 3- (2-methyl-1-propenyl) -2,2-dimethylcyclopropanecarboxylate, 2,3,5,6-tetrafluoro Pyreth such as -4-methoxybenzyl 3-methoxyiminomethyl-2,2-dimethylcyclopropanecarboxylate Id based insecticidal compounds. These compounds may have isomers based on a cyclopropane ring and a double bond. In this case, any active isomer can be used.

本発明の殺虫液は沸点180〜280℃の直鎖ないし分岐鎖状飽和炭化水素系溶剤、ジョチュウギクエキス、フェノール系酸化防止、必要に応じて安定化剤、香料、他の害虫防除性化合物、防カビ剤、他の消臭剤を混合することにより製造することができる。   The insecticidal solution of the present invention is a linear or branched saturated hydrocarbon solvent having a boiling point of 180 to 280 ° C., chrysanthemum extract, phenolic antioxidant, if necessary, stabilizer, fragrance, other pest control compound It can be produced by mixing an antifungal agent and other deodorant.

本発明の殺虫方法は、例えば特公平2−25885号公報等に記載の加熱蒸散型殺虫装置に適用して、優れた効果をあげることができる。この装置では通常、本発明の加熱蒸散用殺虫液中に、多孔質吸液芯の一部(通常は下部)を浸漬して、該芯に前記殺虫液を吸液させ、該芯の非浸漬部(通常は上部)をヒータ等により間接加熱することにより吸液された前記殺虫液を、害虫の発生する場所で、蒸散させることにより行われる。
より具体的には図1に本方法に用いられる装置の一例を示すものであり、殺虫液1中に多孔質吸液芯3の一部が浸漬されており、該芯に該殺虫液を吸液させ、該芯の上部を発熱体2で加熱することができるようになっている。該芯の上部を約60℃〜約135℃の温度に加熱体2で間接加熱することにより、該芯に吸液された本殺虫液を大気中に蒸散させて、害虫を防除することができる。また、この場合の加熱温度は、ヒータの表面温度が通常80〜300℃、好ましくは100〜200℃である。
該加熱蒸散装置において使用される多孔質吸液芯の材質としては、例えば本発明の加熱蒸散用殺虫液を吸液し、かつヒータ等による加熱に耐え得る多孔質の無機物粘結体や焼結体が挙げられる。該多孔質材としては、例えばクレー、タルク、カオリン、珪藻土、石膏、パーライト、ベントナイト、酸性白土、グラスファイバー、石綿等の無機粉末を、カルボキシメチルセルロース、澱粉、アラビアガム、ゼラチン、ポリビニルアルコール等の糊剤にて粘結、成形したものが通常用いられる。尚、該吸液芯は、色素、防腐剤、酸化防止剤等を適宜含有してもよく、例えば、前記無機粉末と糊剤との粘結時に混合することにより含有させることができる。
The insecticidal method of the present invention can be applied to a heat evaporation type insecticidal device described in, for example, Japanese Patent Publication No. 2-25885, and can provide excellent effects. In this apparatus, usually, a part (usually the lower part) of the porous absorbent core is immersed in the insecticidal solution for heat evaporation of the present invention, the insecticide is absorbed into the core, and the core is not immersed. It is carried out by evaporating the insecticide sucked by indirectly heating the part (usually the upper part) with a heater or the like at a place where pests are generated.
More specifically, FIG. 1 shows an example of an apparatus used in this method. A part of the porous absorbent core 3 is immersed in the insecticide 1, and the insecticide is absorbed by the core. The upper part of the core can be heated by the heating element 2. By indirectly heating the upper part of the lead to a temperature of about 60 ° C. to about 135 ° C. with the heating element 2, the insecticide sucked by the lead can be evaporated in the atmosphere to control pests. . The heating temperature in this case is such that the surface temperature of the heater is usually 80 to 300 ° C, preferably 100 to 200 ° C.
The material of the porous liquid absorbent core used in the heating transpiration device is, for example, a porous inorganic caking body or sintered body that absorbs the heat transpiration insecticide of the present invention and can withstand heating by a heater or the like. The body is mentioned. Examples of the porous material include clay, talc, kaolin, diatomaceous earth, gypsum, perlite, bentonite, acid clay, glass fiber, asbestos and other inorganic powders, pastes such as carboxymethylcellulose, starch, gum arabic, gelatin, polyvinyl alcohol and the like. Those that are caking and molded with an agent are usually used. In addition, this liquid absorption core may contain a pigment | dye, antiseptic | preservative, antioxidant, etc. suitably, for example, can be contained by mixing at the time of caking of the said inorganic powder and a paste.

本殺虫液の防除対象害虫としては各種の有害昆虫、ダニ類等の節足動物を挙げることができ、特に有害飛翔性害虫、例えばアカイエカ、コガタアカイエカ、ネッタイイエカ、チカイエカ等のイエカ類、ネッタイシマカ、ヒトスジシマカ等のヤブカ類、シナハマダラカ等のハマダラカ類、ユスリカ類、イエバエ、オオイエバエ、ヒメイエバエ等のイエバエ類、クロバエ類、ニクバエ類、ショウジョウバエ類、チョウバエ類、ノミバエ類、アブ類、ブユ類、サシバエ類、ヌカカ類等の双翅目害虫が挙げられる。   Examples of pests to be controlled by this insecticide include various harmful insects, arthropods such as ticks, and particularly harmful flying pests, for example, Culex mosquitoes such as Akaieka, Kogataakaeka, Attaikaeka, Chikaieka, Aedes aegypti, Aedes albopictus, etc. Aedes, Aedes, Chironomidae, Chironomidae, Houseflies, Drosophila, Drosophila, etc. Diptera pests.

以下、製造例等により本発明を更に詳しく説明するが、本発明はこれらに限定されるものではない。 Hereinafter, the present invention will be described in more detail with reference to production examples, but the present invention is not limited thereto.

製剤例1
ジュチュウギクエキス(純度76%)6.7gとBHT1.3gをノルパー13(エクソン化学株式会社製)92.0gとを混合して、本発明の殺虫液1を得た。

製剤例2
ジュチュウギクエキス(純度76%)6.7gとBHT1.3gをアイソパーM(エクソン化学株式会社製)92.0gとを混合して、本発明の殺虫液2を得た。

製剤例3
ジュチュウギクエキス(純度76%)6.7gとBHT1.3gをネオチオゾール(中央化成株式会社製)92.0gとを混合して、本発明の殺虫液3を得た。

比較例1
ジュチュウギクエキス(純度76%)6.7gをアイソパーM(エクソン化学株式会社製)93.3gとを混合して、比較例1の溶液を得た。

比較例2
ジュチュウギクエキス(純度76%)6.7gとBHT1.3gをアイソパーM(エクソン化学株式会社製)42.0gとを混合して、比較例2の溶液を得た。
Formulation Example 1
An insecticide 1 according to the present invention was obtained by mixing 6.7 g of jujube extract (purity 76%) and 1.3 g of BHT with 92.0 g of Norper 13 (manufactured by Exxon Chemical Co., Ltd.).

Formulation Example 2
An insecticide 2 of the present invention was obtained by mixing 6.7 g of jujube extract (purity 76%) and 1.3 g of BHT with 92.0 g of Isopar M (manufactured by Exxon Chemical Co., Ltd.).

Formulation Example 3
An insecticidal solution 3 of the present invention was obtained by mixing 6.7 g of jujube extract (purity 76%) and 1.3 g of BHT with 92.0 g of neothiozole (manufactured by Chuo Kasei Co., Ltd.).

Comparative Example 1
A solution of Comparative Example 1 was obtained by mixing 6.7 g of jujube extract (purity 76%) with 93.3 g of Isopar M (Exxon Chemical Co., Ltd.).

Comparative Example 2
A solution of Comparative Example 2 was obtained by mixing 6.7 g of jujube extract (purity 76%) and 1.3 g of BHT with 42.0 g of Isopar M (manufactured by Exxon Chemical Co., Ltd.).

(試験例1)
製造例2で得られた本発明の殺虫液45mlを図1の50mlの容器に入れて、無機多孔質材質の吸液芯を取り付けた。この容器を図1に示される加熱蒸散装置に組み込み、吸液芯上部をヒーターで間接的に100時間加熱し続けてから、本発明の殺虫液を試験空間で稼動直後から有効成分が蒸散できるようにした。
この装置をガラスチャンバー(0.7m×0.7m×0.7m:0.34m)の床中央部に置いて10分間稼動させてから、アカイエカ雌成虫を20頭放飼して、フリーフライング状態とした。虫を放飼してから5、7、10、 15、20、30、40および60分後にノックダウン数を調査し時間の経過に伴うノックダウン数から、KT50値を算出した。結果を表2に示す。

(比較試験例1)
比較例1で得られた本発明の殺虫液45mlを図1の50mlの容器に入れて、無機多孔質材質の吸液芯を取り付けた。この容器を図1に示される加熱蒸散装置に組み込み、吸液芯上部をヒーターで間接的に100時間加熱し続けてから、本発明の殺虫液が試験空間で稼動開始直後から有効成分が蒸散できるようにした。
この装置をガラスチャンバー(0.7m×0.7m×0.7m:0.34m)の床中央部に置いて10分間稼動させてから、アカイエカ雌成虫を20頭放飼して、フリーフライング状態とした。虫を放飼してから5、7、10、 15、20、30、40および60分後にノックダウン数を調査し時間の経過に伴うノックダウン数から、KT50値を算出した。結果を表2に示す。

(比較試験例2)
比較例2で得られた本発明の殺虫液45mlを図1の50mlの容器に入れて、無機多孔質材質の吸液芯を取り付けた。この容器を図1に示される加熱蒸散装置に組み込み、吸液芯上部をヒーターで間接的に100時間加熱し続けてから、本発明の殺虫液が試験空間で稼動開始直後から有効成分が蒸散できるようにした。
この装置をガラスチャンバー(0.7m×0.7m×0.7m:0.34m)の床中央部に置いて10分間稼動させてから、アカイエカ雌成虫を20頭放飼して、フリーフライング状態とした。虫を放飼してから5,7、10、 15、20、30、40および60分後にノックダウン数を調査し時間の経過に伴うノックダウン数から、KT50値を算出した。なお、比較例2については吸液芯の詰まりによる効力低下が確認されたので、芯部分をアセトンにつけて洗浄してから1時間加熱後、再度試験した。結果を表2に示す。
(Test Example 1)
45 ml of the insecticidal solution of the present invention obtained in Production Example 2 was placed in a 50 ml container shown in FIG. 1, and a liquid absorbent core made of an inorganic porous material was attached. This container is incorporated into the heating and transpiration device shown in FIG. 1, and the upper portion of the liquid absorption core is continuously heated indirectly by a heater for 100 hours so that the active ingredient can be transpirated immediately after operation of the insecticide of the present invention in the test space. I made it.
This apparatus is placed on the center of the floor of a glass chamber (0.7 m × 0.7 m × 0.7 m: 0.34 m 3 ) and operated for 10 minutes. After that, 20 female squids are released and free flying. State. 5, 7, 10 insects after the release, from the knock number down over the course of a to time investigate the number of knocked down after 15, 20, 30, 40 and 60 minutes, were calculated KT 50 value. The results are shown in Table 2.

(Comparative Test Example 1)
45 ml of the insecticidal solution of the present invention obtained in Comparative Example 1 was placed in the 50 ml container of FIG. 1 and a liquid absorbent core made of an inorganic porous material was attached. This container is incorporated in the heating and transpiration device shown in FIG. 1, and the upper part of the liquid absorption core is indirectly heated with a heater for 100 hours, and then the active ingredient can evaporate immediately after the insecticidal solution of the present invention starts operation in the test space. I did it.
This apparatus is placed on the center of the floor of a glass chamber (0.7 m × 0.7 m × 0.7 m: 0.34 m 3 ) and operated for 10 minutes. After that, 20 female squids are released and free flying. State. 5, 7, 10 insects after the release, from the knock number down over the course of a to time investigate the number of knocked down after 15, 20, 30, 40 and 60 minutes, were calculated KT 50 value. The results are shown in Table 2.

(Comparative Test Example 2)
45 ml of the insecticidal solution of the present invention obtained in Comparative Example 2 was placed in a 50 ml container of FIG. 1 and a liquid absorbent core made of an inorganic porous material was attached. This container is incorporated in the heating and transpiration device shown in FIG. 1, and the upper part of the liquid absorption core is indirectly heated with a heater for 100 hours, and then the active ingredient can evaporate immediately after the insecticidal solution of the present invention starts operation in the test space. I did it.
This apparatus is placed on the center of the floor of a glass chamber (0.7 m × 0.7 m × 0.7 m: 0.34 m 3 ) and operated for 10 minutes. After that, 20 female squids are released and free flying. State. The number of knockdowns was investigated 5, 7, 10, 15, 20, 30, 40, and 60 minutes after releasing the insects, and the KT50 value was calculated from the number of knockdowns over time. In Comparative Example 2, since a decrease in efficacy due to clogging of the liquid absorbent core was confirmed, the core portion was washed with acetone and heated for 1 hour, and then tested again. The results are shown in Table 2.

Figure 2006282643
表2に示すように殺虫液2は安定した害虫防除効果を示したが、酸化防止剤を加えない場合や濃度が濃すぎる場合には効果が劣った。
Figure 2006282643
As shown in Table 2, the insecticide 2 showed a stable pest control effect, but the effect was poor when no antioxidant was added or when the concentration was too high.

本発明の殺虫方法に適用される装置の一例の断面図Sectional drawing of an example of the apparatus applied to the insecticidal method of this invention

符号の説明Explanation of symbols

1・・・殺虫液
2・・・ヒーター
3・・・吸液芯
4・・・殺虫液を入れる容器。
DESCRIPTION OF SYMBOLS 1 ... Insecticide 2 ... Heater 3 ... Liquid absorption core 4 ... Container which puts an insecticide.

Claims (3)

50%留出温度が200〜300℃の直鎖ないし分岐鎖状飽和炭化水素(以下、(a)成分と記す。)を60〜99.99重量%とジョチュウギクエキス(以下、(b)成分と記す。)を0.01〜10重量%およびフェノール系酸化防止剤(以下、(c)成分と記す。)を0.01〜10重量%含有することを特徴とする加熱蒸散用害虫防除液 60 to 99.99% by weight of straight chain or branched saturated hydrocarbon (hereinafter referred to as component (a)) having a 50% distillation temperature of 200 to 300 ° C. and chrysanthemum extract (hereinafter referred to as (b) Pest control for heating transpiration, characterized by containing 0.01 to 10% by weight and 0.01 to 10% by weight of a phenolic antioxidant (hereinafter referred to as component (c)). liquid 請求項1に記載の加熱蒸散用害虫防除液中に多孔質吸液芯の一部を浸漬して、該芯に害虫防除液を吸わせながら、該芯の非浸漬部分を加熱することにより吸液された害虫防除液を大気中に蒸散させて害虫を駆除する方法
A part of the porous liquid absorbent core is immersed in the pest control liquid for heat evaporation according to claim 1, and the non-immersed part of the core is heated by sucking the pest control liquid while the core absorbs the pest control liquid. A method of exterminating pests by evaporating the liquid pest control solution into the atmosphere
加熱温度が150〜280℃である請求項1記載の害虫防除方法


The pest control method according to claim 1, wherein the heating temperature is 150 to 280 ° C.


JP2005108595A 2005-04-05 2005-04-05 Insect pest control solution for heating transpiration containing pyrethrum extract as effective component and method of insect pest control Pending JP2006282643A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009062282A (en) * 2007-09-04 2009-03-26 Hakugen:Kk Extermination method of cockroach
CN102511477A (en) * 2011-11-28 2012-06-27 华南农业大学 Pyrethrin hot fogging agent and preparation method and application thereof
CN105123350A (en) * 2015-07-13 2015-12-09 重庆市彭水琳琅农业发展有限公司 Organic control method for fly and insect attack on shaddocks

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009062282A (en) * 2007-09-04 2009-03-26 Hakugen:Kk Extermination method of cockroach
CN102511477A (en) * 2011-11-28 2012-06-27 华南农业大学 Pyrethrin hot fogging agent and preparation method and application thereof
CN105123350A (en) * 2015-07-13 2015-12-09 重庆市彭水琳琅农业发展有限公司 Organic control method for fly and insect attack on shaddocks

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