JPS5935521Y2 - heating evaporation plate - Google Patents

heating evaporation plate

Info

Publication number
JPS5935521Y2
JPS5935521Y2 JP7875479U JP7875479U JPS5935521Y2 JP S5935521 Y2 JPS5935521 Y2 JP S5935521Y2 JP 7875479 U JP7875479 U JP 7875479U JP 7875479 U JP7875479 U JP 7875479U JP S5935521 Y2 JPS5935521 Y2 JP S5935521Y2
Authority
JP
Japan
Prior art keywords
plate
transpiration
evaporation plate
present
drug
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.)
Expired
Application number
JP7875479U
Other languages
Japanese (ja)
Other versions
JPS55180436U (en
Inventor
博志 平松
良春 高砂
隆啓 長谷川
正富 大塚
Original Assignee
ア−ス製薬株式会社
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 ア−ス製薬株式会社 filed Critical ア−ス製薬株式会社
Priority to JP7875479U priority Critical patent/JPS5935521Y2/en
Publication of JPS55180436U publication Critical patent/JPS55180436U/ja
Application granted granted Critical
Publication of JPS5935521Y2 publication Critical patent/JPS5935521Y2/en
Expired legal-status Critical Current

Links

Description

【考案の詳細な説明】 本考案は加熱蒸散板に関する。[Detailed explanation of the idea] The present invention relates to a heating evaporation plate.

従来加熱蒸散板は、例えば電気蚊取器に代表されるよう
に、電気的に加熱される熱板上に載置されることにより
、薬剤を蒸散させて殺虫等の目的に用いられるいわゆる
殺虫マットであり、バルブや石綿等を主とする繊維板等
の基材に加熱蒸散用薬剤を溶剤溶液等の形態で塗布含浸
されている。
Conventional heating evaporation plates are so-called insecticidal mats that are used for purposes such as killing insects by evaporating chemicals by placing them on an electrically heated hot plate, as typified by electric mosquito repellents. A chemical for heating and evaporation is applied and impregnated in the form of a solvent solution to a base material such as a fiberboard or the like, which is mainly made of bulbs or asbestos.

このような殺虫マットは既に各種のものが市販されてお
り、その形状、大きさに関してはいずれも略々同じで゛
あって、3.5mmX22mmX3.0〜3.2mm(
肉厚)の板状基材の全体に薬剤を含浸保持させている。
Various types of such insecticidal mats are already commercially available, and they are all approximately the same in shape and size: 3.5 mm x 22 mm x 3.0 to 3.2 mm (
The drug is impregnated and retained throughout the plate-like base material (thick).

ところがこのような公知の殺虫マットに於ては、これが
比較的厚肉(3,0〜3.2mm)であるので、熱板を
加熱してから薬剤が蒸散されるまでに時間を要すると共
に、マット内部の温度勾配が大きいために使用後の薬剤
残存率が大きく例えば25〜30%にも達し不経済であ
った。
However, since such known insecticidal mats have a relatively thick wall (3.0 to 3.2 mm), it takes time for the chemicals to evaporate after the hot plate is heated, and Since the temperature gradient inside the mat is large, the residual rate of the drug after use is high, reaching, for example, 25 to 30%, making it uneconomical.

本考案者はこのような問題を解決することを目的として
蒸散板の厚みを市販品よりも薄くすることを試みたとこ
ろ、蒸散開始時間及び残存率の改善はみられるものの、
これでは薬剤の蒸散が加熱開始後の短時間に集中し薬効
持続時間が極度に低下するという問題を招くことが判っ
た。
In order to solve this problem, the present inventor attempted to make the thickness of the transpiration plate thinner than commercially available products, and although improvements were seen in the transpiration start time and survival rate,
It has been found that this causes a problem in that the transpiration of the drug concentrates in a short period of time after the start of heating, and the duration of the drug's efficacy is extremely reduced.

そこで本考案者は、蒸散板の厚みを薄くすることに加え
、蒸散面の周縁部の少なくとも一部に突起部を形式する
ときは、薬効持続時間を殆んど低下することなしに、蒸
散開始時間及び残存率の問題を一掃し得ることを見出し
、鼓に本考案を完成するに至ったものである。
Therefore, in addition to reducing the thickness of the transpiration plate, the inventor of the present invention found that when a protrusion is formed on at least a part of the peripheral edge of the transpiration surface, transpiration can be started without substantially reducing the duration of the medicinal effect. It was discovered that the problems of time and survival rate could be eliminated, and the present invention was finally completed.

即ち本考案は蒸散板の全体に含浸保持された薬剤を加熱
蒸散する形式の加熱蒸散板において、蒸散板の厚みが0
.5〜2.8mmであって、がっ蒸散板の蒸散面の周縁
部の一部又は全部が突起部を形成していることを特徴と
する加熱蒸散板に係る。
That is, the present invention is a heating evaporation plate that heats and evaporates the drug impregnated throughout the evaporation plate, and the thickness of the evaporation plate is 0.
.. The heating evaporation plate has a diameter of 5 to 2.8 mm and is characterized in that a part or all of the peripheral edge of the evaporation surface of the evaporation plate forms a protrusion.

本考案による加熱蒸散板によれば薬効を長時間持続保持
し、従来品と同様に殺虫マットとして支障なく使用でき
ると共に、蒸散使用初期段階の蒸散性が向上し加熱開始
後速みやかに所定の薬効を発揮でき、更に含有薬剤の残
存率が低下し、薬剤を無駄なく有効に蒸散使用できる特
長を有する。
The heating evaporation plate of the present invention maintains its medicinal efficacy for a long time and can be used as an insecticidal mat without any problems like conventional products.In addition, the transpiration performance in the initial stage of transpiration use is improved, and the specified level can be quickly reached after heating starts. It has the characteristics of being able to exhibit medicinal efficacy, and furthermore, the residual rate of the contained drug is reduced, and the drug can be effectively evaporated and used without wasting it.

本考案に於て、加熱蒸散板の形状、大きさは任意であり
、形状は矩形、正方形、三角形、ひし形、楕円形、円形
等を例示でき、大きさは使用される熱源例えば電気蚊取
器の放熱板の大きさに応じ決められる。
In the present invention, the shape and size of the heating evaporation plate are arbitrary, and examples include rectangular, square, triangular, diamond, oval, and circular shapes, and the size depends on the heat source used, such as an electric mosquito repellent. It is decided according to the size of the heat sink.

本考案に於て、突起部は蒸散面の周縁部の全周に形式さ
れる場合と一部に形成される場合があり、一部の場合に
は例えば対向する2辺に沿って形成するようにすればよ
い。
In the present invention, the protrusion may be formed all around the periphery of the transpiration surface, or may be formed on a part of the periphery of the transpiration surface, and in some cases, for example, it may be formed along two opposing sides. Just do it.

本考案に於て上記蒸散板の突起部の形成手段は任意であ
り、例えば多少厚目の蒸散板用基材を用意し、金型を利
用してプレスにより形成する方法等を上げうる。
In the present invention, the protrusions of the evaporation plate can be formed by any means, such as preparing a somewhat thick base material for the evaporation plate and forming them by pressing using a mold.

本考案に於ては蒸散使用の初期段階に於ける薬剤の蒸散
性向上を目的として、突起部以外の蒸散面に凹凸部を形
成することができる。
In the present invention, uneven parts can be formed on the transpiration surface other than the protrusions for the purpose of improving the transpiration performance of the drug in the initial stage of transpiration use.

これとは逆に使用終期段階での蒸散性の向上を目的とす
る場合には、突起部の上面に凹凸部を設ければよい。
On the contrary, if the purpose is to improve the transpiration performance at the final stage of use, an uneven portion may be provided on the upper surface of the protrusion.

上記蒸散板に保持される薬剤としては、従来より害虫駆
除、殺菌、賦香等の目的に使用されている各種の薬剤を
使用できる。
As the chemicals held in the transpiration plate, various chemicals conventionally used for purposes such as pest control, sterilization, and fragrance can be used.

殺虫剤例えばピレスロイドである一般名アレスリン及び
アレスリンの幾可及び/又は光学異性体、比較的蒸気圧
の高いピレスロイドなど、忌避剤例えばN、 N−ジエ
チル−メタ−トルアミド、シクロヘキシミドなど、殺菌
剤例えばサリチル酸、パラクロロ−メタ−キシレノール
など、賦香剤例えばレモン系、ローズ系、グリーン系な
どの各種香料を例示できる。
Insecticides such as the pyrethroid, common name allethrin and several and/or optical isomers of allethrin, pyrethroids with relatively high vapor pressure, repellents such as N,N-diethyl-meta-toluamide, cycloheximide, etc., fungicides such as salicylic acid. , parachloro-meta-xylenol, etc., and various flavoring agents such as lemon-based, rose-based, and green-based fragrances.

代表的薬剤としては以下のものを例示できる。The following are examples of representative drugs.

03−アリル−2−メチルシクロペンタ−2−エン4−
オン−1−イル d−シス/トランスークリサンテマー
ト (以下ピナミンフォルテという)05−ベンジル−
3−フリルメチル d−シス/トランスークリサンテマ
ート(以下クリスロンフォルテという) 03−フェノキシベンジル d−シス/トランスクリサ
ンテマート (以下スミスリンという)03−フェノキ
シベンジル 3−(2,2−ジクロロヒニル)−2,2
−ジメチルシクロプロパンカルボキシレート (以下ペ
ルメトリンという)○ エムペンスリン(住友化学工業
株式会社製、商品名:ペーパースリン) 00.0−ジメチル 0−(2,2−ジクロロ)ビニル
ホスフェート (以下DDVPという)00.0−ジメ
チル 0−(3−メチル−4−ニトロフェニル)チオノ
フォスフェート(以下スミチオンという) 00.0−ジメチル−5−(1,2−ジカルボエトキシ
エチル)ジチオフォスフェート (以下マラソンという
) 本考案において上記薬剤には、通常用いられている効力
増強剤(ピペロニルブトキサイド、サイネピレン222
等)、消臭剤(ラウリル酸メタクリレート等)、香料(
シトラール、シトロネラール等)の各種添加剤を任意に
添加することができる。
03-allyl-2-methylcyclopent-2-ene 4-
On-1-yl d-cis/trans-chrysanthemate (hereinafter referred to as pinamine forte) 05-benzyl-
3-furylmethyl d-cis/trans-chrysanthemate (hereinafter referred to as cryuronforte) 03-phenoxybenzyl d-cis/trans-chrysanthemate (hereinafter referred to as smithrin) 03-phenoxybenzyl 3-(2,2-dichlorohinyl) -2,2
-Dimethylcyclopropanecarboxylate (hereinafter referred to as permethrin) ○ Empenthrin (manufactured by Sumitomo Chemical Co., Ltd., trade name: Paper Surin) 00.0-Dimethyl 0-(2,2-dichloro)vinyl phosphate (hereinafter referred to as DDVP) 00. 0-dimethyl 0-(3-methyl-4-nitrophenyl) thionophosphate (hereinafter referred to as sumithion) 0-dimethyl-5-(1,2-dicarboethoxyethyl) dithiophosphate (hereinafter referred to as marathon) In the present invention, the above drugs include commonly used potency enhancers (piperonyl butoxide, sinepyrene 222,
etc.), deodorants (lauric acid methacrylate, etc.), fragrances (
Various additives such as citral, citronellal, etc.) can be optionally added.

本考案に於て、加熱蒸散板の材質としては石綿、岩綿等
の無機繊維、パルプ等並びに無機粉末を成形して板状と
したもの等を例示できる。
In the present invention, examples of the material for the heating evaporation plate include inorganic fibers such as asbestos and rock wool, pulp, and inorganic powder formed into a plate shape.

なお上記蒸散板の被加熱面にアルミニウム等の熱伝導性
シートあるいは断熱性シートを貼り合わせてもよい 本考案に於て、加熱蒸散板の厚みは0.5〜2.8mm
であって、厚みが0.5mmより薄い場合は単位面積当
りの薬剤保持量に自づと制約を受は好ましくない。
In the present invention, a thermally conductive sheet or a heat insulating sheet made of aluminum or the like may be attached to the heated surface of the evaporation plate, and the thickness of the heating evaporation plate is 0.5 to 2.8 mm.
Therefore, if the thickness is thinner than 0.5 mm, it is not preferable that the amount of drug held per unit area is naturally limited.

また2、8mmを超えると厚み方向への熱の伝達が不充
分となり良好な薬剤蒸散が困難となる。
Moreover, if the thickness exceeds 2.8 mm, heat transfer in the thickness direction becomes insufficient, making it difficult to evaporate the chemical well.

以下に本考案を図示した本考案実施の1例を示す図面に
もとづき説明すると次の通りである。
The present invention will be described below with reference to drawings showing an example of the implementation of the present invention.

第1〜8図は本考案実施の1例を示す平面図A及び断面
図Bであり、第1〜3図に於て、1は加熱蒸散板であり
、該蒸散板1の周縁部に突起部2が周設されている場合
を示し、該突起部2が上記蒸散板1の蒸散面に設けられ
ている。
1 to 8 are a plan view A and a sectional view B showing an example of the implementation of the present invention. A case is shown in which a portion 2 is provided around the periphery, and the protrusion portion 2 is provided on the evaporation surface of the evaporation plate 1.

第4〜5図は該突起部2が上記蒸散板の両側部に設けら
れており、この場合も蒸散面側だけに該突起部2が形成
されている。
In FIGS. 4 and 5, the projections 2 are provided on both sides of the evaporation plate, and in this case, the projections 2 are also formed only on the evaporation surface side.

第6〜8図は第1〜3図の変更例を示すもので、加熱蒸
散板1の蒸散面側に凸凹部3が設けられている。
6 to 8 show modifications of FIGS. 1 to 3, in which uneven portions 3 are provided on the evaporation surface side of the heating evaporation plate 1. FIGS.

以下に本考案品〔第1図乃至第8図に図示のもの、寸法
:35mX22mmX1.5mm (突起部2.8mm
))]と、本考案品とは突起部を有しない以外は同一の
比較1(但し肉厚: 2.8 mm)及び比較2(但し
、肉厚:1.5mm)と、更に市販1 (但し肉厚:3
.0mm)及び市販2(但し肉厚:3.2mm)とを、
薬剤含有量を同一にして、市販の同一電気蚊取器を用い
て、揮散量、残存量について比較した結果を第1表に示
す。
The following is a product of the present invention [as shown in Figures 1 to 8, dimensions: 35m x 22mm x 1.5mm (protrusion 2.8mm)
))], Comparison 1 (wall thickness: 2.8 mm) and Comparison 2 (wall thickness: 1.5 mm), which are the same as the invented product except that it does not have a protrusion, and commercially available 1 ( However, wall thickness: 3
.. 0 mm) and commercially available 2 (however, wall thickness: 3.2 mm),
Table 1 shows the results of comparing the volatilization amount and residual amount using the same commercially available electric mosquito repellent with the same drug content.

尚アレスリンの光学異性体であるピナミンフォルテ(商
品名、住友化学工業株式会社製)40mg及びピペロニ
ルブトキサイド40 mgを各種肉厚の35mm X
22 mmのリンターパルプよりなる加熱蒸散板基材の
全体に含浸させて各種試料を作成し、これを表面150
°Cの電気蚊取器の熱板上に載置した。
In addition, 40 mg of Pinamin Forte (trade name, manufactured by Sumitomo Chemical Industries, Ltd.), which is an optical isomer of allethrin, and 40 mg of piperonyl butoxide were added to 35 mm X
Various samples were prepared by impregnating the entire heated evaporation plate base material made of 22 mm linter pulp, and the surface 150
It was placed on the hot plate of an electric mosquito repellent at °C.

第1表から明かなように、比較1及び2と市販1及び2
は、9〜10時間の時間帯に於ける有効揮散率が、殺蚊
効力の限界といわれる6%にいずれも達しておらず、薬
効持続性に問題があり、また比較1と市販1及び2は残
存率が20〜30%にも達し薬剤ロスが大きい。
As is clear from Table 1, comparative 1 and 2 and commercially available 1 and 2
The effective volatilization rate in the 9-10 hour period did not reach 6%, which is said to be the limit of mosquitoicidal efficacy, and there was a problem with the durability of the drug's efficacy. The residual rate is as high as 20-30%, resulting in large drug losses.

更に0〜1時間の時間帯に於ける有効揮散率に於ても、
市販1及び2は、5%前後でいずれも6%に達していな
い。
Furthermore, regarding the effective volatilization rate in the time period of 0 to 1 hour,
Commercially available products 1 and 2 have a content of around 5%, neither of which has reached 6%.

之に対し本考案によるものは、0〜1.4〜5及び9〜
10の時間帯の全てに於て有効揮散率が6%を遥かに越
え、少なくとも10時間に亘って薬効を持続できる。
On the other hand, those according to the present invention have a range of 0 to 1.4 to 5 and 9 to 1.
The effective volatilization rate far exceeds 6% in all 10 time periods, and the medicinal efficacy can be sustained for at least 10 hours.

更に残存率に於ても市販1及び2に比べ少なくとも30
%程度低減でき、経済性を向上できる。
Furthermore, the residual rate is at least 30% higher than that of commercially available 1 and 2.
%, improving economic efficiency.

更に0〜1時間の時間帯に於ける有効揮散率に於ても6
%台を遥かに越え、加熱開始後、速みやかに所定の薬効
を発揮し得る。
Furthermore, the effective volatilization rate in the time period of 0 to 1 hour was also 6.
% range, and the desired medicinal effect can be exerted immediately after heating starts.

このように本考案に於ては、薬効持続性時間を何等低下
することなしに、蒸散性及び残存率を著るしく改善でき
る。
As described above, in the present invention, the transpiration property and the residual rate can be significantly improved without any decrease in the duration of drug efficacy.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図乃至第8図は、相異なる本考案の実施例を示す平
面図A及び断面図Bである。 図に於いて、1は蒸散板、2は突起部、3は凹凸部であ
る。
1 to 8 are a plan view A and a sectional view B showing different embodiments of the present invention. In the figure, 1 is a transpiration plate, 2 is a protrusion, and 3 is an uneven portion.

Claims (1)

【実用新案登録請求の範囲】[Scope of utility model registration request] 蒸散板の全体に含浸保持された薬剤を加熱蒸散する形式
の加熱蒸散板において、蒸散板の厚みが0.5〜2.8
mmであって、かつ蒸散板の蒸散面の周縁部の一部又は
全部が突起部を形式していることを特徴とする加熱蒸散
板。
In a heating evaporation plate that heats and evaporates the drug impregnated and retained throughout the transpiration plate, the thickness of the transpiration plate is 0.5 to 2.8.
1. mm, and a part or all of the peripheral edge of the evaporation surface of the evaporation plate is in the form of a protrusion.
JP7875479U 1979-06-08 1979-06-08 heating evaporation plate Expired JPS5935521Y2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7875479U JPS5935521Y2 (en) 1979-06-08 1979-06-08 heating evaporation plate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7875479U JPS5935521Y2 (en) 1979-06-08 1979-06-08 heating evaporation plate

Publications (2)

Publication Number Publication Date
JPS55180436U JPS55180436U (en) 1980-12-25
JPS5935521Y2 true JPS5935521Y2 (en) 1984-10-01

Family

ID=29312202

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7875479U Expired JPS5935521Y2 (en) 1979-06-08 1979-06-08 heating evaporation plate

Country Status (1)

Country Link
JP (1) JPS5935521Y2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60126202A (en) * 1983-12-09 1985-07-05 Fumakiraa Kk Insecticidal sheet

Also Published As

Publication number Publication date
JPS55180436U (en) 1980-12-25

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