JPH10182306A - Insecticidal liquid for heat transpiration - Google Patents
Insecticidal liquid for heat transpirationInfo
- Publication number
- JPH10182306A JPH10182306A JP8343452A JP34345296A JPH10182306A JP H10182306 A JPH10182306 A JP H10182306A JP 8343452 A JP8343452 A JP 8343452A JP 34345296 A JP34345296 A JP 34345296A JP H10182306 A JPH10182306 A JP H10182306A
- Authority
- JP
- Japan
- Prior art keywords
- insecticidal
- solution
- carbon atoms
- heat
- insecticide
- 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.)
- Pending
Links
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、加熱蒸散用殺虫液
及び加熱蒸散殺虫方法に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an insecticidal solution for heat evaporation and a method of heat evaporation.
【0002】[0002]
【発明が解決しようとする課題】殺虫液中に吸液芯の一
部を浸漬して該芯に殺虫液を吸液させ、該芯の殺虫液中
に浸漬されていない部分を加熱することにより吸液され
た殺虫液を蒸散させる加熱蒸散殺虫方法において、加熱
蒸散過程における殺虫液組成の変化等により、長時間に
わたって安定した殺虫液の蒸散を行い、安定した殺虫効
果を得ることが困難であることから、安定した蒸散を可
能とし、安定した殺虫効果をあげることのできる加熱蒸
散用殺虫液の開発が望まれていた。A part of a liquid absorbing core is immersed in an insecticide to absorb the insecticide into the core, and a portion of the core not immersed in the insecticide is heated. In the heat evaporation insecticidal method of evaporating the absorbed insecticide, it is difficult to perform stable evaporation of the insecticide over a long period of time due to a change in the insecticide composition during the heat evaporation process, and to obtain a stable insecticidal effect. Therefore, development of an insecticidal solution for heat transpiration that enables stable transpiration and achieves a stable insecticidal effect has been desired.
【0003】[0003]
【従来の技術】これに対して、特開平7−196418
号公報には、有効成分としてフラメトリン、アレスリ
ン、プラレトリン、ベンフルスリン(トランスフルスリ
ン)0.3〜5.0 重量%を油性溶剤に溶解した加熱蒸散用
殺虫液において、該油性溶剤として沸点範囲が200 〜30
0 ℃のノルマルパラフィンに加え、沸点範囲が250 〜35
0℃のイソパラフィン及び/又はナフテン系炭化水素を1
0〜70重量%用いることが提唱されているが、該方法に
おいても、加熱蒸散初期及び終期における蒸散の安定性
は必ずしも充分ではない。2. Description of the Related Art On the other hand, Japanese Patent Application Laid-Open No. 7-196418
The publication discloses that in a pesticidal solution for heat evaporation in which 0.3 to 5.0% by weight of flamethrin, allethrin, praletrin, and benfluthulin (transfluthrin) are dissolved as an active ingredient in an oily solvent, the boiling point range of the oily solvent is 200 to 30.
In addition to normal paraffin at 0 ° C, the boiling point range is 250-35.
Isoparaffin and / or naphthenic hydrocarbon at 0 ° C
Although it is proposed to use 0 to 70% by weight, even in this method, the stability of evaporation at the beginning and end of evaporation is not always sufficient.
【0004】[0004]
【課題を解決するための手段】本発明は、上述の課題を
解決するものであり、殺虫活性成分が、炭素数16〜2
0のノルマルパラフィンと共に、炭素数10〜15のイ
ソパラフィン系及び/又はナフテン系炭化水素に溶解さ
れてなる殺虫液を用いることにより、殺虫液及び殺虫活
性成分の安定した蒸散を可能とし、その結果、長時間に
わたって安定した殺虫効力を維持することを可能とした
ものである。即ち、本発明は殺虫液中に吸液芯の一部を
浸漬して該芯に殺虫液を吸液させ、吸液芯の殺虫液中に
浸漬されていない部分を加熱することにより吸液された
殺虫液を蒸散させる加熱蒸散殺虫方法に用いられる殺虫
液において、殺虫活性成分が、炭素数16〜20のノル
マルパラフィンと共に、炭素数10〜15のイソパラフ
ィン系及び/又はナフテン系炭化水素に溶解されてなる
加熱蒸散用殺虫液、並びに、該殺虫液を用いる加熱蒸散
殺虫方法を提供するものである。SUMMARY OF THE INVENTION The present invention has been made to solve the above-mentioned problems, and has a pesticidal active ingredient containing 16 to 2 carbon atoms.
By using an insecticide solution dissolved in an isoparaffinic and / or naphthenic hydrocarbon having 10 to 15 carbon atoms together with normal paraffin of 0, it is possible to stably evaporate the insecticide solution and the insecticidal active ingredient. It is possible to maintain a stable insecticidal effect for a long time. That is, in the present invention, a part of the absorbent core is immersed in the insecticide, the insecticide is absorbed into the core, and the part of the absorbent core that is not immersed in the insecticide is heated to absorb the liquid. In the insecticidal solution used in the heat transpiration insecticidal method for evaporating the insecticidal solution, the insecticidal active ingredient is dissolved in isoparaffinic and / or naphthenic hydrocarbons having 10 to 15 carbon atoms together with normal paraffins having 16 to 20 carbon atoms. The present invention provides an insecticidal solution for heat transpiration and a method for heat transpiration and insecticidal use of the insecticide.
【0005】[0005]
【発明の実施の形態】本発明において用いられる殺虫活
性成分としては、殺虫効力や安全性等の点からピレスロ
イド化合物の使用が好ましく、該ピレスロイド化合物と
しては、アレスリン、プラレトリン、フラメトリン、エ
ムペントリン、レスメトリン、フェノトリン、ペルメト
リン、トランスフルスリン、テラレスリン、シラフルオ
フェン、エトフェンプロックス、1−エチニル−2−フ
ルオロ−2−ペンテニル 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
ト等が挙げられ、本発明の加熱蒸散用殺虫液中に通常0.
1 〜5重量%含有される。BEST MODE FOR CARRYING OUT THE INVENTION As the insecticidal active ingredient used in the present invention, use of a pyrethroid compound is preferred from the viewpoint of insecticidal efficacy and safety. Examples include phenothrin, permethrin, transfluthrin, teraresulin, silafluofen, etofenprox, 1-ethynyl-2-fluoro-2-pentenyl 3- (2,2-dichlorovinyl) -2,2-dimethylcyclopropanecarboxylate, and the like. Is usually contained in the insecticidal solution for heat evaporation of the present invention.
It is contained in an amount of 1 to 5% by weight.
【0006】本発明において用いられる炭素数16〜2
0のノルマルパラフィンとは、直鎖のアルカンであるヘ
キサデカン、ヘプタデカン、オクタデカン、ノナデカ
ン、エイコサン及びこれらの混合物であり、本発明の加
熱蒸散用殺虫液中に通常5〜45重量%、好ましくは8
〜40重量%含有される。The carbon number of 16 to 2 used in the present invention
The normal paraffin of 0 is a linear alkane such as hexadecane, heptadecane, octadecane, nonadecane, eicosane and a mixture thereof, and is usually 5 to 45% by weight, preferably 8% by weight in the insecticidal solution for heat evaporation of the present invention.
-40% by weight.
【0007】本発明において用いられる炭素数10〜1
5のイソパラフィン系炭化水素(側鎖のある飽和炭化水
素)としては、例えばエクソン化学株式会社製のアイソ
パーM(炭素数12〜15のイソパラフィン系炭化水素
を主成分とする炭化水素溶媒)、アイソパーL(炭素数
11〜13のイソパラフィン系炭化水素を主成分とする
炭化水素溶媒)、アイソパーH(炭素数11〜12のイ
ソパラフィン系炭化水素を主成分とする炭化水素溶
媒)、アイソパーG(炭素数10〜11のイソパラフィ
ン系炭化水素を主成分とする炭化水素溶媒)、出光石油
化学株式会社製のIPソルベント1620(炭素数10〜1
5のイソパラフィン系炭化水素を主成分とする炭化水素
溶媒)、日本石油化学株式会社製の日石アイソゾール30
0 (炭素数10〜13のイソパラフィン系炭化水素を主
成分とする炭化水素溶媒)、シェルジャパン株式会社品
のシェルゾール71(炭素数10〜12のイソパラフィン
系炭化水素を主成分とする炭化水素溶媒)、シェルゾー
ル72(炭素数11〜15のイソパラフィン系炭化水素を
主成分とする炭化水素溶媒)、昭和化成株式会社品のメ
ルベイユ40(炭素数11〜15のイソパラフィン系炭化
水素を主成分とする炭化水素溶媒)、メルベイユ30(炭
素数10〜12のイソパラフィン系炭化水素を主成分と
する炭化水素溶媒)等が挙げられる。[0007] The carbon number 10-1 used in the present invention
Examples of the isoparaffin-based hydrocarbon (saturated hydrocarbon having a side chain) of No. 5 include, for example, Isopar M (hydrocarbon solvent mainly composed of an isoparaffin-based hydrocarbon having 12 to 15 carbon atoms) manufactured by Exxon Chemical Co., Ltd. (Hydrocarbon solvent mainly containing isoparaffinic hydrocarbons having 11 to 13 carbon atoms), Isopar H (hydrocarbon solvent mainly containing isoparaffinic hydrocarbons having 11 to 12 carbon atoms), Isopar G (hydrocarbon solvent having 10 carbon atoms) To 11 isoparaffinic hydrocarbons), IP Solvent 1620 manufactured by Idemitsu Petrochemical Co., Ltd.
5, a hydrocarbon solvent containing an isoparaffinic hydrocarbon as a main component), Nisseki Isosol 30 manufactured by Nippon Petrochemical Co., Ltd.
0 (hydrocarbon solvent mainly containing isoparaffinic hydrocarbon having 10 to 13 carbon atoms), Shellsol 71 manufactured by Shell Japan Co., Ltd. (hydrocarbon solvent mainly containing isoparaffinic hydrocarbon having 10 to 12 carbon atoms) ), Shellsol 72 (hydrocarbon solvent mainly composed of an isoparaffinic hydrocarbon having 11 to 15 carbon atoms), Merveille 40 manufactured by Showa Kasei Co., Ltd. (mainly composed of an isoparaffinic hydrocarbon having 11 to 15 carbon atoms) Hydrocarbon solvents), Merveille 30 (a hydrocarbon solvent mainly composed of an isoparaffinic hydrocarbon having 10 to 12 carbon atoms), and the like.
【0008】また、炭素数10〜15のナフテン系炭化
水素(シクロパラフィン;環式飽和炭化水素)として
は、例えば日本石油化学株式会社製の日石ナフテゾール
H(炭素数15のナフテン系炭化水素を主成分とする炭
化水素溶媒)、日石ナフテゾールM(炭素数12〜13
のナフテン系炭化水素を主成分とする炭化水素溶媒)、
日石ナフテゾールL(炭素数10〜11のナフテン系炭
化水素を主成分とする炭化水素溶媒)、日本石油株式会
社製のAFソルベント−4(炭素数14のナフテン系炭
化水素を主成分とする炭化水素溶媒)、シェルジャパン
株式会社品のシェルゾールD−70(炭素数12〜13
のナフテン系炭化水素を主成分とする炭化水素溶媒)等
が挙げられる。さらに、炭素数10〜15のイソパラフ
ィン系炭化水素と炭素数10〜15のナフテン系炭化水
素とを主成分とするエクソン化学株式会社製のエクソー
ルD−80(炭素数10〜13のナフテン系及びイソパ
ラフィン系炭化水素溶媒を主成分とする炭化水素溶
媒)、エクソールD−110(炭素数15のナフテン系
及びイソパラフィン系炭化水素溶媒を主成分とする炭化
水素溶媒)等が挙げられる。The naphthenic hydrocarbons having 10 to 15 carbon atoms (cycloparaffins; cyclic saturated hydrocarbons) include, for example, Nippon Petrochemical Co., Ltd. Nisseki Naphthesol H (a naphthenic hydrocarbon having 15 carbon atoms). A hydrocarbon solvent as a main component), Nisseki Naphthesol M (C12-13)
A hydrocarbon solvent whose main component is a naphthenic hydrocarbon),
Nisseki Naphthesol L (hydrocarbon solvent mainly containing naphthenic hydrocarbons having 10 to 11 carbon atoms), AF Solvent-4 manufactured by Nippon Oil Co., Ltd. (carbonization mainly containing naphthenic hydrocarbons having 14 carbon atoms) Hydrogen solvent), Shell Japan Co., Ltd. Shellsol D-70 (C12-13)
(A hydrocarbon solvent whose main component is a naphthenic hydrocarbon). Furthermore, Exol D-80 (a naphthenic and isoparaffin having 10 to 13 carbon atoms) manufactured by Exxon Chemical Co., Ltd., which mainly comprises an isoparaffinic hydrocarbon having 10 to 15 carbon atoms and a naphthenic hydrocarbon having 10 to 15 carbon atoms. Exol D-110 (a hydrocarbon solvent mainly composed of a naphthene-based and isoparaffin-based hydrocarbon solvent having 15 carbon atoms), and the like.
【0009】本発明の加熱蒸散用殺虫液は、炭素数10
〜15のイソパラフィン系及び/又はナフテン系炭化水
素を主構成成分とするものであり、該イソパラフィン系
及び/又はナフテン系炭化水素は、通常、本発明の加熱
蒸散用殺虫液中に55〜95重量%含有される。尚、本
発明の加熱蒸散用殺虫液は、殺虫活性成分、炭素数16
〜20のノルマルパラフィン、炭素数10〜15のイソ
パラフィン系及び/又はナフテン系炭化水素の他に、必
要により、殺菌剤、共力剤、芳香剤等を含有してもよ
い。また、BHT、BHA等のフェノール系安定化剤、
ベンゾフェノン系又はベンゾトリアゾール系等の紫外線
吸収剤などの安定化剤、エステル等の揮散調整剤を含有
してもよい。The insecticidal solution for heat evaporation of the present invention has a carbon number of 10
-15-isoparaffinic and / or naphthenic hydrocarbons as a main component, and the isoparaffinic and / or naphthenic hydrocarbons are usually 55 to 95% by weight in the insecticidal solution for heat evaporation of the present invention. %. The insecticidal solution for heat evaporation according to the present invention contains an insecticidally active ingredient having 16 carbon atoms.
In addition to normal paraffins having up to 20 carbon atoms, isoparaffinic and / or naphthenic hydrocarbons having 10 to 15 carbon atoms, a bactericide, a synergist, a fragrance and the like may be contained as necessary. Phenolic stabilizers such as BHT and BHA;
It may contain a stabilizer such as a benzophenone-based or benzotriazole-based ultraviolet absorber and a volatilization modifier such as an ester.
【0010】本発明の加熱蒸散殺虫方法は、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、カ、ハエ等の衛生害虫を始め種々の害虫防
除に優れた効果をあげることができる。図1は本発明の
加熱蒸散殺虫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の一部を浸漬されて
おり、該芯に殺虫液を吸液させ、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。The heat-transpiration insecticidal method of the present invention is excellent in controlling various insect pests including sanitary pests such as mosquitoes and flies by applying it to a heat-transpiration type insecticidal apparatus described in, for example, Japanese Patent Publication No. 25885/1990. The effect can be improved. FIG. 1 shows an example of an apparatus used in the heat transpiration insecticidal method of the present invention, in which a part of a porous absorbent core 3 is immersed in an insecticide solution 1 and the insecticide solution is absorbed in the core. And the upper part of the core is heated 2
So that it can be heated.
【0011】吸液芯の材質としては、通常、多孔質材が
用いられ、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、石綿等の無機粉末又
は耐熱性高分子樹脂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、必要により焼成したもの
が用いられる。また、耐熱性高分子樹脂粉末を熱可塑性
樹脂で固結させて得られるものを用いてもよい。尚、該
吸液芯に、色素、防腐剤等を適宜添加してもよい。As the material of the liquid absorbing core, a porous material is usually used. Examples of the porous material include clay, talc, kaolin, diatomaceous earth, gypsum, perlite, bentonite, acid clay, glass fiber, asbestos and the like. Inorganic powder or heat-resistant polymer resin powder of the above is bonded with a paste such as carboxymethylcellulose, starch, gum arabic, gelatin, polyvinyl alcohol, etc., molded and, if necessary, fired. Further, a material obtained by consolidating a heat-resistant polymer resin powder with a thermoplastic resin may be used. In addition, a coloring matter, a preservative, and the like may be appropriately added to the absorbent core.
【0012】[0012]
【実施例】以下、本発明を実施例をあげてより詳細に説
明する。まず、本発明の加熱蒸散用殺虫液の製造例を示
す。 製造例1 プラレトリン1.7 重量部及びヘプタデカン20重量部をア
イソパーM(エクソン化学株式会社製;炭素数12〜1
5のイソパラフィン系炭化水素を主成分とする炭化水素
溶媒)に溶解して全体を100 重量部とし、本発明の殺虫
液を得た。The present invention will be described below in more detail with reference to examples. First, a production example of the insecticidal solution for heat evaporation of the present invention will be described. Production Example 1 1.7 parts by weight of praretrin and 20 parts by weight of heptadecane were obtained from Isopar M (manufactured by Exxon Chemical Co., Ltd .;
5), and the whole was made up to 100 parts by weight to obtain an insecticidal solution of the present invention.
【0013】製造例2 プラレトリン1.7 重量部及びヘプタデカン30重量部をエ
クソールD−80(エクソン化学株式会社製;炭素数1
0〜13のナフテン系炭化水素を45〜50重量%、炭素数
10〜13のイソパラフィン系炭化水素を約35重量%含
有する炭化水素溶媒)に溶解して全体を100 重量部と
し、本発明の殺虫液を得た。Production Example 2 1.7 parts by weight of praretrin and 30 parts by weight of heptadecane were added to Exol D-80 (manufactured by Exxon Chemical Co., Ltd .;
A hydrocarbon solvent containing 45 to 50% by weight of a naphthenic hydrocarbon of 0 to 13 and about 35% by weight of an isoparaffinic hydrocarbon of 10 to 13 carbon atoms) to make the whole 100 parts by weight. An insecticidal solution was obtained.
【0014】製造例3 プラレトリン1.7 重量部及びオクタデカン10重量部をア
イソパーMに溶解して全体を100 重量部とし、本発明の
殺虫液を得た。Production Example 3 1.7 parts by weight of praletrin and 10 parts by weight of octadecane were dissolved in Isopar M to make the whole 100 parts by weight, thereby obtaining an insecticidal solution of the present invention.
【0015】製造例4 プラレトリン1.7 重量部及びノナデカン10重量部をアイ
ソパーMに溶解して全体を100 重量部とし、本発明の殺
虫液を得た。Production Example 4 1.7 parts by weight of praletrin and 10 parts by weight of nonadecane were dissolved in Isopar M to make the whole 100 parts by weight, thereby obtaining an insecticidal solution of the present invention.
【0016】次に、後述の試験例で比較のために用いる
殺虫液の製造例を参考例として示す。 参考例1 プラレトリン1.7 重量部及びペンタデカン20重量部をエ
クソールD−130(エクソン化学株式会社製;炭素数
16以上のナフテン系炭化水素を主成分とする溶媒)に
溶解して全体を100 重量部とし、比較用の殺虫液を得
た。Next, a production example of an insecticidal solution used for comparison in a test example described later is shown as a reference example. Reference Example 1 1.7 parts by weight of praletrin and 20 parts by weight of pentadecane were dissolved in Exol D-130 (manufactured by Exxon Chemical Co., Ltd .; a solvent mainly composed of a naphthenic hydrocarbon having 16 or more carbon atoms) to make the whole 100 parts by weight. Thus, an insecticidal solution for comparison was obtained.
【0017】参考例2 プラレトリン1.7 重量部及びペンタデカン40重量部をエ
クソールD−130に溶解して全体を100 重量部とし、
比較用の殺虫液を得た。Reference Example 2 1.7 parts by weight of praletrin and 40 parts by weight of pentadecane were dissolved in Exol D-130 to make the whole 100 parts by weight.
An insecticidal solution for comparison was obtained.
【0018】参考例3 プラレトリン1.7 重量部をネオチオゾール(中央化成株
式会社製;炭素数12〜15のノルマルパラフィン)に
溶解して全体を100 重量部とし、比較用の殺虫液を得
た。Reference Example 3 1.7 parts by weight of praletrin was dissolved in neothiozole (manufactured by Chuo Kasei Co., Ltd .; normal paraffin having 12 to 15 carbon atoms) to make the whole 100 parts by weight, to obtain an insecticidal solution for comparison.
【0019】次に試験例を示す。 試験例 製造例1〜4の各々で得た殺虫液を45ml容の容器に入
れて吸液芯(無機粉末を糊剤で粘結して得られる多孔質
材)を取付け、図1に示されるような加熱蒸散型殺虫装
置に設置した。直径4cm、高さ12cmのガラス管内にアカ
イエカ雌成虫10頭を放ち、ガラス管の両端をナイロン網
で閉じたもの2本をプラスチック製筒状カバー(直径18
cm、高さ30cm)内に入れて垂直方向に保持し、該筒状カ
バーの下に金属筒(直径20cm、高さ80cm)を設置し、そ
の金属筒底部に予め加熱した図1に示される加熱蒸散型
殺虫装置を設置し、吸液芯上部を120〜135℃に間
接加熱してアカイエカがノックダウンする虫数を数え、
プロビット法によりKT50値(50%の虫がノックダウ
ンするのに要する時間、単位は分)を計算した。また、
参考例1〜3で得た殺虫液についても比較のために同様
の試験を行った。結果を表1に示す。Next, test examples will be described. Test Example The insecticidal solution obtained in each of Production Examples 1 to 4 was placed in a 45-ml container, and a liquid-absorbing core (a porous material obtained by binding inorganic powder with a paste) was attached, as shown in FIG. It installed in such a heat evaporation type insecticidal apparatus. 10 adult female Culex pipiens pallens are released into a glass tube 4 cm in diameter and 12 cm in height, and two glass tubes whose both ends are closed with nylon mesh are covered with a plastic cylindrical cover (diameter 18).
cm, height 30 cm) and held vertically, a metal cylinder (diameter 20 cm, height 80 cm) was placed under the cylindrical cover and the bottom of the metal cylinder was preheated as shown in FIG. Install a heat transpiration type insecticidal device, indirectly heat the upper part of the absorbent core to 120-135 ° C, count the number of insects that Culex pipiens knock down,
The KT 50 value (the time required for 50% of the insects to knock down, in minutes) was calculated by the probit method. Also,
The same test was performed for the insecticidal solutions obtained in Reference Examples 1 to 3 for comparison. Table 1 shows the results.
【0020】[0020]
【表1】 [Table 1]
【0021】上表の結果に見られるように、沸点が270
℃のペンタデカンと沸点範囲が277〜310 ℃のエクソー
ルD−130とを溶媒に用いた(特開平7-196418号公報
参照)参考例1及び2の殺虫液では、全体に殺虫効力の
低下が見られ、特に初期及び終期における殺虫効力の低
下が大きく、また、ノルマルパラフィンのみを溶媒に用
いた参考例3の殺虫液では、終期における殺虫効力の著
しい低下が見られた。これに対して、本発明の殺虫液で
は、ほぼ一定の殺虫効力を持続させることができた。As can be seen from the results in the above table, the boiling point was 270.
In the insecticidal solutions of Reference Examples 1 and 2, in which pentadecane at a temperature of 0 ° C. and Exol D-130 having a boiling point range of 277 to 310 ° C. were used as solvents (see JP-A-7-196418), a decrease in insecticidal efficacy was observed as a whole. In particular, the insecticidal efficacy was significantly reduced at the initial and final stages, and the insecticidal solution of Reference Example 3 using only normal paraffin as the solvent showed a remarkable decrease at the final stage. In contrast, the insecticidal solution of the present invention was able to maintain almost constant insecticidal efficacy.
【0022】[0022]
【発明の効果】本発明の加熱蒸散殺虫方法によれば、長
時間にわたって安定した殺虫液の蒸散を行い、安定した
殺虫効果を得ることができる。According to the method of the present invention, the insecticidal liquid is stably evaporated for a long time to obtain a stable insecticidal effect.
【図1】本発明の加熱蒸散殺虫方法に用いられる装置の
一例を示す説明図である。FIG. 1 is an explanatory diagram showing an example of an apparatus used in the method for killing insects by heat evaporation according to the present invention.
1は殺虫液、2は発熱体、3は吸液芯、4は殺虫液を入
れた容器を表す。Reference numeral 1 denotes an insecticide, 2 denotes a heating element, 3 denotes an absorbent core, and 4 denotes a container containing the insecticide.
Claims (4)
殺虫液を吸液させ、吸液芯の殺虫液中に浸漬されていな
い部分を加熱することにより吸液された殺虫液を蒸散さ
せる加熱蒸散殺虫方法に用いられる殺虫液において、殺
虫活性成分が、炭素数16〜20のノルマルパラフィン
と共に、炭素数10〜15のイソパラフィン系及び/又
はナフテン系炭化水素に溶解されてなることを特徴とす
る加熱蒸散用殺虫液。A liquid absorbent core is immersed in a pesticide solution to absorb the insecticide into the wick, and a portion of the absorbent core that is not immersed in the insecticide solution is heated to absorb the liquid. In the insecticidal solution used in the heat transpiration insecticidal method for evaporating the insecticidal solution, the insecticidal active ingredient is dissolved in isoparaffinic and / or naphthenic hydrocarbons having 10 to 15 carbon atoms together with normal paraffins having 16 to 20 carbon atoms. An insecticidal solution for heat transpiration characterized by comprising:
ラフィン含有量が5〜45重量%である請求項1記載の
加熱蒸散用殺虫液。2. The insecticidal solution for heat evaporation according to claim 1, wherein the content of the normal paraffin having 16 to 20 carbon atoms in the insecticide solution is 5 to 45% by weight.
請求項1又は請求項2記載の加熱蒸散用殺虫液。3. The insecticidal solution for heat evaporation according to claim 1, wherein the insecticidal active ingredient is a pyrethroid compound.
殺虫液を吸液させ、吸液芯の殺虫液中に浸漬されていな
い部分を加熱することにより吸液された殺虫液を蒸散さ
せる加熱蒸散殺虫方法において、殺虫活性成分が、炭素
数16〜20のノルマルパラフィンと共に、炭素数10
〜15のイソパラフィン系及び/又はナフテン系炭化水
素に溶解されてなる殺虫液を用いることを特徴とする加
熱蒸散殺虫方法。4. A liquid absorbent core is immersed in an insecticide solution to absorb the insecticide solution into the wick, and a portion of the absorbent core not immersed in the insecticide solution is heated to absorb the liquid. In a heat-transpiration insecticidal method for evaporating a pesticidal solution, the insecticidal active component is a mixture of normal paraffin having 16 to 20 carbon atoms and 10 normal carbon atoms.
A heat-transpiration insecticidal method, which comprises using an insecticide solution dissolved in isoparaffinic and / or naphthenic hydrocarbons.
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8343452A JPH10182306A (en) | 1996-12-24 | 1996-12-24 | Insecticidal liquid for heat transpiration |
ES9702633A ES2129378B1 (en) | 1996-12-24 | 1997-12-18 | LIQUID INSECTICIDE PREPARATION FOR THERMAL FUMIGATION AND METHOD FOR REPRESSING INSECTS BY THERMAL FUMIGATION. |
BR9706414A BR9706414A (en) | 1996-12-24 | 1997-12-19 | Insecticidal liquid preparation for hot fumigation process to control insects by hot fumigation and hot fumigation device |
ARP970106098 AR010381A1 (en) | 1996-12-24 | 1997-12-22 | LIQUID INSECTICIDE PREPARATION, METHOD FOR REPRESSING INSECTS BY THERMAL FUMIGATION WITH THE SAME AND APPARATUS OF THE TYPE FOR THERMAL FUMIGATION QUELA USA |
CN97125907A CN1185899A (en) | 1996-12-24 | 1997-12-23 | Liquid insecticidal preparation for heat fumigation and method for controlling insects by heat fumigation |
IT97RM000807 IT1297138B1 (en) | 1996-12-24 | 1997-12-23 | PREPARATION LIQUID INSECTICIDE FOR HOT FUMIGATION AND PROCEDURE TO CONTROL INSECTS FOR HOT FUMIGATION |
IDP973983A ID19221A (en) | 1996-12-24 | 1997-12-24 | LIQUID INSECTICIDE PROVISIONS FOR HEAT-FUMIGATION AND INSECT CONTROL METHOD THROUGH HEAT-FUMIGATION |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8343452A JPH10182306A (en) | 1996-12-24 | 1996-12-24 | Insecticidal liquid for heat transpiration |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH10182306A true JPH10182306A (en) | 1998-07-07 |
Family
ID=18361633
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8343452A Pending JPH10182306A (en) | 1996-12-24 | 1996-12-24 | Insecticidal liquid for heat transpiration |
Country Status (7)
Country | Link |
---|---|
JP (1) | JPH10182306A (en) |
CN (1) | CN1185899A (en) |
AR (1) | AR010381A1 (en) |
BR (1) | BR9706414A (en) |
ES (1) | ES2129378B1 (en) |
ID (1) | ID19221A (en) |
IT (1) | IT1297138B1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001342103A (en) * | 2000-03-31 | 2001-12-11 | Sumitomo Chem Co Ltd | Liquid insecticide for thermal evaporation and insecticidal thermal evaporation method using the insecticide |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102524312A (en) * | 2012-01-15 | 2012-07-04 | 陈谐晷 | Natural pyrethrin hot smoke agent and use method thereof |
TWI586274B (en) * | 2015-04-14 | 2017-06-11 | Dainippon Jochugiku Kk | Insect pest control product and insect pest control method |
CN108684701A (en) * | 2018-07-25 | 2018-10-23 | 成都彩虹电器(集团)股份有限公司 | A kind of composition and product of mosquito |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54135227A (en) * | 1978-04-13 | 1979-10-20 | Kureha Chem Ind Co Ltd | Insecticidal or fungicidal fumigant |
EG18025A (en) * | 1986-07-18 | 1993-06-30 | Sumitomo Chemical Co | A method for killing insects by heating fumigation |
JPS63152305A (en) * | 1986-08-15 | 1988-06-24 | Fumakiraa Kk | Insecticidal mat for vaporization by heating |
JPH07196418A (en) * | 1993-12-28 | 1995-08-01 | Dainippon Jochugiku Co Ltd | Liquid type thermo-transpiring insecticidal composition and insecticidal method |
AU708907B2 (en) * | 1995-09-14 | 1999-08-12 | Sumitomo Chemical Company, Limited | Liquid insecticidal preparation for heat fumigation and method for killing insects by heat fumigation |
-
1996
- 1996-12-24 JP JP8343452A patent/JPH10182306A/en active Pending
-
1997
- 1997-12-18 ES ES9702633A patent/ES2129378B1/en not_active Expired - Lifetime
- 1997-12-19 BR BR9706414A patent/BR9706414A/en not_active Application Discontinuation
- 1997-12-22 AR ARP970106098 patent/AR010381A1/en unknown
- 1997-12-23 IT IT97RM000807 patent/IT1297138B1/en active IP Right Grant
- 1997-12-23 CN CN97125907A patent/CN1185899A/en active Pending
- 1997-12-24 ID IDP973983A patent/ID19221A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001342103A (en) * | 2000-03-31 | 2001-12-11 | Sumitomo Chem Co Ltd | Liquid insecticide for thermal evaporation and insecticidal thermal evaporation method using the insecticide |
Also Published As
Publication number | Publication date |
---|---|
IT1297138B1 (en) | 1999-08-03 |
BR9706414A (en) | 1999-05-18 |
CN1185899A (en) | 1998-07-01 |
ES2129378A1 (en) | 1999-06-01 |
ID19221A (en) | 1998-06-28 |
ES2129378B1 (en) | 2000-01-16 |
ITRM970807A1 (en) | 1999-06-23 |
AR010381A1 (en) | 2000-06-07 |
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