JPS63130502A - Insecticidal mat - Google Patents

Insecticidal mat

Info

Publication number
JPS63130502A
JPS63130502A JP27755386A JP27755386A JPS63130502A JP S63130502 A JPS63130502 A JP S63130502A JP 27755386 A JP27755386 A JP 27755386A JP 27755386 A JP27755386 A JP 27755386A JP S63130502 A JPS63130502 A JP S63130502A
Authority
JP
Japan
Prior art keywords
insecticidal
mat
volatile
heating
cyclodextrin
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
Application number
JP27755386A
Other languages
Japanese (ja)
Inventor
Mareyoshi Sawaguchi
希能 澤口
Michio Kawada
川田 倫夫
Yutaka Aoki
豊 青木
Takashi Kawasaki
隆志 川崎
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nitto Denko Corp
Original Assignee
Nitto Electric Industrial Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nitto Electric Industrial Co Ltd filed Critical Nitto Electric Industrial Co Ltd
Priority to JP27755386A priority Critical patent/JPS63130502A/en
Publication of JPS63130502A publication Critical patent/JPS63130502A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain an insecticidal mat having excellent preservation quality and thermal stability, by including a volatile insecticidal ingredient in cyclodextrin and placing the resultant clathrate material on a mat. CONSTITUTION:An insecticidal mat obtained by including a volatile insecticidal ingredient, particularly preferably pyrethroid based insecticide in cyclodextrin, particularly preferably beta-type and placing the resultant clathrate material on a mat. Oxidation of the volatile insecticidal ingredient can be prevented and stability to light is improved by including the volatile insecticidal ingredient. The volatility thereof by heating is as good as that of the nonclathrate compound. That is, since the volatile insecticidal ingredient is stably present even in preservation of the insecticidal mat as well as in use while heating and moderately volatilized in use while heating, excellent insecticidal effects are sustained for a long period. There is no fear of toxicity without requiring use of noxious oxidizing agents.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、殺虫マットに関するものであり、特にそこに
含有される揮発性殺虫成分が保存性および熱安定性に優
れている殺虫マットに関するものであ。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to an insecticidal mat, and particularly to an insecticidal mat in which volatile insecticidal components contained therein have excellent storage stability and thermal stability. So.

〔従来技術・発明が解決しようとする問題点〕従来、電
気蚊とりマットをはじめとする加熱式殺虫マットは、揮
発性殺虫成分、たとえばピレスロイドを厚紙等に含有せ
しめたものが主である。
[Prior Art/Problems to be Solved by the Invention] Conventionally, heating type insecticidal mats such as electric mosquito repellent mats have mainly been made of cardboard containing volatile insecticidal ingredients such as pyrethroids.

ところが、かかる殺虫マットは、加熱使用中あるいは保
存中に、揮発性殺虫成分が酸化分解して効果が充分に発
揮されないことが多い。
However, in such insecticidal mats, the volatile insecticidal components are often oxidized and decomposed during heating or storage, resulting in insufficient effectiveness.

また、この酸化分解を防止するためにBHAやBITと
いった酸化防止剤を多量に含有せしめていた。このため
、気化されたBHAやBITの空気中濃度が数百1)I
)Mにも至るケースが報告され、人体に対する慢性、急
性毒性(安全性)に対する配慮を求める報告もしばしば
あり、これらに対する対策が社会的にも要求されるよう
になっている。
Furthermore, in order to prevent this oxidative decomposition, a large amount of antioxidants such as BHA and BIT have been contained. For this reason, the concentration of vaporized BHA and BIT in the air is several hundred 1) I
) M, and there are also reports that often call for consideration of chronic and acute toxicity (safety) to the human body, and social measures are also becoming required.

従って、本発明は加熱使用中あるいは保存中にも、揮発
性殺虫成分が安定である殺虫マットを提供することであ
る。
Therefore, it is an object of the present invention to provide an insecticidal mat whose volatile insecticidal components are stable even during heating and storage.

〔問題点を解決するための手段〕[Means for solving problems]

本発明者らは、かかる目的を達成するために種々研究を
続けてきたところ、サイクロデキストリンに揮発性殺虫
成分を包接させることにより、揮発性殺虫成分の酸化が
防止されること、光に対する安定性にも優れること、し
かも加熱による揮発性は非包接化合物と同様に良好であ
り、従ってBHA、BITなどの酸化防止剤を必要とし
ないで、安定で優れた殺虫特性が得られることを見出し
、さらに研究を重ねて本発明を完成するに至った。
The present inventors have continued various studies to achieve this objective, and have found that by including volatile insecticidal ingredients in cyclodextrin, oxidation of the volatile insecticidal ingredients can be prevented and that the volatile insecticidal ingredients can be stabilized against light. Furthermore, we discovered that its volatility upon heating is as good as that of non-clathrate compounds, and that stable and excellent insecticidal properties can be obtained without the need for antioxidants such as BHA and BIT. After further research, the present invention was completed.

即ち、本発明はサイクロデキストリンに包接されてなる
揮発性殺虫成分(以下、包接化合物ともいう)をマット
に配してなる殺虫マットである。
That is, the present invention is an insecticidal mat in which a volatile insecticidal component (hereinafter also referred to as an clathrate compound) encapsulated in cyclodextrin is arranged on the mat.

本発明で使用される揮発性殺虫成分は、揮発すること(
特に、180℃程度の加熱下に揮散して殺虫活性を示す
ものが好ましい)によって殺虫活性を示し、サイクロデ
キストリンに包接されうる化合物であれば特に制限はな
い。揮発性殺虫成分としてはピレスロイド類が一般に使
用され、合成のもの、天然のもののいずれであってもよ
い。合成のピレスロイドとしてはアレスリン、フレスリ
ン、ピレトリン、ペルメトリン等が、天然のピレスロイ
ドとしては除虫菊中の成分、たとえば、ピレスリン1)
ピレスリン■、シネリン■、シネリン■等が例示される
The volatile insecticidal component used in the present invention has the ability to volatilize (
There are no particular limitations as long as the compound exhibits insecticidal activity by volatilizing under heating at about 180° C. and can be included in cyclodextrin. Pyrethroids are generally used as volatile insecticidal ingredients, and they may be either synthetic or natural. Synthetic pyrethroids include allethrin, fresrin, pyrethrin, permethrin, etc.; natural pyrethroids include components of pyrethrum, such as pyrethrin 1)
Examples include pyrethrin (■), cinerin (■), and cinerin (■).

本発明の殺虫マットに使用されるマットとしては、従来
この分野で使用されているものを使用すれば充分であり
、揮発性殺虫成分を配しえ、たとえば180℃程度の加
熱に対して耐熱性を有するものが使用される。かかるも
のの具体例としては、たとえば厚紙、フェルト、石膏ボ
ード、石綿紙、木片等が例示される。マットの厚みには
特に制限はないが、適度の揮発性を維持できる等の観点
から0.1〜3龍程度のものが、好適に使用される。
As the mat used in the insecticidal mat of the present invention, it is sufficient to use one conventionally used in this field, which can contain volatile insecticidal ingredients and is heat resistant to heating of about 180 degrees Celsius. The one with the following is used. Specific examples of such materials include cardboard, felt, plasterboard, asbestos paper, and wood chips. There is no particular limit to the thickness of the mat, but from the viewpoint of maintaining appropriate volatility, a thickness of about 0.1 to 3 mm is preferably used.

本発明で使用されるサイクロデキストリンとしては、α
、β、γタイプのいずれでもよいが、特にβタイプのも
のが好ましい。
The cyclodextrin used in the present invention includes α
, β, and γ types, but β type is particularly preferred.

揮発性殺虫成分のサイクロデキストリンへの包接は自体
既知の手段、たとえば次のようにして簡便に行われる。
Inclusion of volatile insecticidal components into cyclodextrin is conveniently carried out by means known per se, for example, as follows.

即ち、サイクロデキストリン水溶液に、揮発性殺虫成分
を有m?8媒(たとえば、エタノール等)に溶解したも
のを徐々に加えて包接化合物を沈澱させて濾取する手段
等が例示される。
That is, does the cyclodextrin aqueous solution contain volatile insecticidal components? An example of such a method is to gradually add a solution dissolved in an 8 medium (for example, ethanol, etc.) to precipitate the clathrate and filter it out.

この場合、エチレンジアミン四酢酸のようなキレート剤
を存在させることが望ましい。
In this case, it is desirable to have a chelating agent such as ethylenediaminetetraacetic acid present.

包接化合物をマットに配する態様として、マ。Ma is a mode of disposing the clathrate compound on the mat.

トの内部に包接化合物が浸透した態様のみならず、マッ
ト表面に華に付着したC、様をも包含するものであるが
、好ましくはマットの内部にまで包接化合物が侵透した
態様のものが使用される。具体的な方法としては、包接
化合物を溶媒(たとえばポリビニルアルコール、エタノ
ール1:グリセリン3:水60の混合溶媒など)に分散
しマットに直接塗布または含浸後、乾燥する方法などに
よってマットに配される。
This includes not only the embodiment in which the clathrate compound penetrates into the interior of the mat, but also the embodiment in which the clathrate compound penetrates into the interior of the mat, but it also includes the embodiment in which the clathrate compound penetrates into the interior of the mat. things are used. A specific method is to disperse the clathrate compound in a solvent (for example, polyvinyl alcohol, a mixed solvent of 1 part ethanol, 3 parts glycerin, and 60 parts water) and apply it directly to the mat, or apply it directly to the mat and then dry it. Ru.

本発明の包接化合物のマットに配する量には特に制限は
ないが、通常10■〜50■/clI!程度である。
There is no particular limit to the amount of the clathrate compound of the present invention disposed in the mat, but it is usually 10 to 50 μ/clI! That's about it.

本発明の殺虫マットは、たとえば所謂電気蚊取器等にセ
ントされて、90〜180℃程度に加温されて使用され
る。かくして、揮発性の殺虫成分が揮発して良好なる殺
虫活性が発揮される。
The insecticidal mat of the present invention is used, for example, by placing it in a so-called electric mosquito repellent or the like and heating it to about 90 to 180°C. In this way, the volatile insecticidal components are volatilized and good insecticidal activity is exhibited.

〔作用・効果〕[Action/Effect]

本発明の殺虫マットにおいては、揮発性殺虫成分がサイ
クロデキストリンに包接されているので、揮発性殺虫成
分が、当該殺虫マット保存時は勿論、加熱使用にも安定
に存在しえ、かつ加熱使用時に適度に揮発されるので優
れた殺虫効果が長時間持続する。また、BHAやB I
 Tといった有害な酸化防止剤を使用する必要がないの
で、これらに起因する慢性、急性毒性の懸念もない。
In the insecticidal mat of the present invention, since the volatile insecticidal component is included in cyclodextrin, the volatile insecticidal component can stably exist not only during storage of the insecticidal mat but also when heated. Because it evaporates in a moderate amount, its excellent insecticidal effect lasts for a long time. Also, BHA and B I
Since there is no need to use harmful antioxidants such as T, there is no concern about chronic or acute toxicity caused by these.

〔実施例・実験例〕[Example/Experiment example]

実施例1 ピレトリン1gとエチレンジアミン四酢酸0.01gを
エタノール10m1に分散し、これをβ−サイクロデキ
ストリン10%水溶液50m1に徐々に加え、沈澱物を
濾取し、乾燥した。
Example 1 1 g of pyrethrin and 0.01 g of ethylenediaminetetraacetic acid were dispersed in 10 ml of ethanol, and this was gradually added to 50 ml of a 10% β-cyclodextrin aqueous solution, and the precipitate was collected by filtration and dried.

得られた包接化合物300■を含む20%ポリビニルア
ルコール溶/&1mlを厚さ1)、面積1゜ciの厚紙
の表面に塗布し、40℃で乾燥して殺虫マットを得た。
1 ml of a 20% polyvinyl alcohol solution containing 300 μm of the obtained clathrate compound was applied onto the surface of cardboard with a thickness of 1) and an area of 1° ci, and dried at 40° C. to obtain an insecticidal mat.

実施例2 ピレトリン1gの代わりにフレスワン1gを使用し、実
施例1と同様に行って殺虫マットを得た。
Example 2 An insecticidal mat was obtained in the same manner as in Example 1, except that 1 g of Freswan was used instead of 1 g of pyrethrin.

比較例1 ピレトリン1gとエチレンジアミン四酢i90.01g
の混合物を作製し、その100■を含む20%ポリビニ
ルアルコール1)1m+を厚さl mu、面積10cd
の厚紙の表面に塗布し、40℃で乾燥して殺虫マットを
得た。
Comparative Example 1 1 g of pyrethrin and 90.01 g of ethylenediaminetetravinegar i
Prepare a mixture of 20% polyvinyl alcohol containing 100μ of 1) 1m+ of the mixture with a thickness of l mu and an area of 10cd.
It was applied onto the surface of cardboard and dried at 40°C to obtain an insecticidal mat.

比較例2 ピレトリン1gの代わりにフレスリン1gを使用し、比
較例1と同様に行って殺虫マットを得た。
Comparative Example 2 An insecticidal mat was obtained in the same manner as in Comparative Example 1 except that 1 g of Fresrin was used instead of 1 g of pyrethrin.

実験例1 (持続性試験) 実施例1.2および比較例1.2で作製した殺虫マット
を150℃に加熱したホットプレート上に置き、所定時
間加熱後の殺虫マット中の揮発゛性殺虫成分の残存量を
測定した。測定方法は所定時間後、エタノール101に
残存する揮発性殺虫成分を溶解させ、逆相液体クロマト
グラフィーにて定量分析した。なお加熱前の殺虫マット
中の揮発性殺虫成分量を100%として計算し、表1に
示した。
Experimental Example 1 (Sustainability Test) The insecticidal mats prepared in Example 1.2 and Comparative Example 1.2 were placed on a hot plate heated to 150°C, and the volatile insecticidal components in the insecticidal mats were heated for a predetermined period of time. The remaining amount was measured. The measurement method was to dissolve the remaining volatile insecticidal components in ethanol 101 after a predetermined period of time, and perform quantitative analysis using reversed phase liquid chromatography. The calculations are shown in Table 1, assuming that the amount of volatile insecticidal components in the insecticidal mat before heating is 100%.

(以下余白) 表  1 実験例2(耐熱分解性試験) 実施例1.2および比較例1.2で作製した殺虫マット
を細かく裁断し、これを体積200m1のシールドチュ
ーブ中に入れ、密封した。このシールドチューブを18
0℃に加熱したオーブンに入れ、所定時間加熱後の殺虫
マット中の揮発性殺虫成分の残存量を測定した。測定方
法は所定時間後、エタノール10m1に残存する揮発性
殺虫成分を溶解させ、逆相液体クロマトグラフィーにて
定量分析した。なお加熱前の殺虫マット中の揮発性殺虫
成分量を100%として計算し、表2に示した。
(Margins below) Table 1 Experimental Example 2 (Heat decomposition resistance test) The insecticidal mats prepared in Example 1.2 and Comparative Example 1.2 were cut into pieces, placed in a shield tube with a volume of 200 m1, and sealed. This shield tube is 18
The insecticidal mat was placed in an oven heated to 0°C, and after heating for a predetermined period of time, the remaining amount of volatile insecticidal components in the insecticidal mat was measured. The measurement method was to dissolve the remaining volatile insecticidal components in 10 ml of ethanol after a predetermined period of time, and perform quantitative analysis using reversed phase liquid chromatography. The calculations are shown in Table 2, assuming that the amount of volatile insecticidal components in the insecticidal mat before heating is 100%.

表  2 実験例3(保存試験) 実施例1.2および比較例L2で作製した殺虫マットを
ポリエステル/ポリエチレンラミネートフィルム40μ
厚さのものでヒートシールした。
Table 2 Experimental Example 3 (Storage Test) The insecticidal mats prepared in Example 1.2 and Comparative Example L2 were coated with a 40μ polyester/polyethylene laminate film.
I heat sealed it with a thick one.

ヒートシールは大きさ5cmX4.5cm、内周り4.
50X3cmである。このヒートシールを40℃、湿度
90%中で3ケ月保存した後、殺虫マット中の揮発性殺
虫成分の残存量を測定した。測定方法は保存後、エタノ
ール10+wlに残存する揮発性殺虫成分を溶解させ、
逆相液体クロマトグラフィーにて定量分析した。なお保
存前の殺虫マット中の揮発性殺虫成分量を100%とし
て計算し、表3に示した。
Heat seal size: 5cm x 4.5cm, inner circumference: 4.
It is 50 x 3 cm. After this heat seal was stored for 3 months at 40° C. and 90% humidity, the remaining amount of volatile insecticidal components in the insecticidal mat was measured. The measurement method is to dissolve the remaining volatile insecticidal components in ethanol 10+wl after storage,
Quantitative analysis was performed using reverse phase liquid chromatography. Note that calculations were made assuming that the amount of volatile insecticidal components in the insecticidal mat before storage was 100%, and the results are shown in Table 3.

表3Table 3

Claims (3)

【特許請求の範囲】[Claims] (1)サイクロデキストリンに包接されてなる揮発性殺
虫成分をマットに配してなる殺虫マット。
(1) An insecticidal mat in which a volatile insecticidal ingredient encapsulated in cyclodextrin is arranged on the mat.
(2)揮発性殺虫成分がピレスロイド系殺虫剤である特
許請求の範囲第(1)項記載の殺虫マット。
(2) The insecticidal mat according to claim (1), wherein the volatile insecticidal component is a pyrethroid insecticide.
(3)サイクロデキストリンがβタイプである特許請求
の範囲第(1)項記載の殺虫マット。
(3) The insecticidal mat according to claim (1), wherein the cyclodextrin is β type.
JP27755386A 1986-11-20 1986-11-20 Insecticidal mat Pending JPS63130502A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27755386A JPS63130502A (en) 1986-11-20 1986-11-20 Insecticidal mat

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27755386A JPS63130502A (en) 1986-11-20 1986-11-20 Insecticidal mat

Publications (1)

Publication Number Publication Date
JPS63130502A true JPS63130502A (en) 1988-06-02

Family

ID=17585133

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27755386A Pending JPS63130502A (en) 1986-11-20 1986-11-20 Insecticidal mat

Country Status (1)

Country Link
JP (1) JPS63130502A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001058261A2 (en) * 2000-02-11 2001-08-16 The Government Of The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Insecticide-impregnated fabric and method of production
JP2007509853A (en) * 2003-10-27 2007-04-19 エンデュラ ソシエタ ペル アチオニ Synergistic insecticidal composition formulation as a cyclodextrin complex

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001058261A2 (en) * 2000-02-11 2001-08-16 The Government Of The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Insecticide-impregnated fabric and method of production
WO2001058261A3 (en) * 2000-02-11 2002-03-07 Us Health Insecticide-impregnated fabric and method of production
US6896892B2 (en) 2000-02-11 2005-05-24 The United States Of America As Represented By The Department Of Health And Human Services Insecticide-impregnated fabric and method of production
JP2007509853A (en) * 2003-10-27 2007-04-19 エンデュラ ソシエタ ペル アチオニ Synergistic insecticidal composition formulation as a cyclodextrin complex

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