JP2003289781A - Vaporizing apparatus - Google Patents

Vaporizing apparatus

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Publication number
JP2003289781A
JP2003289781A JP2002098560A JP2002098560A JP2003289781A JP 2003289781 A JP2003289781 A JP 2003289781A JP 2002098560 A JP2002098560 A JP 2002098560A JP 2002098560 A JP2002098560 A JP 2002098560A JP 2003289781 A JP2003289781 A JP 2003289781A
Authority
JP
Japan
Prior art keywords
volatile
drug
carrier
fan
embedding material
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
JP2002098560A
Other languages
Japanese (ja)
Inventor
Koichi Taniguchi
晃一 谷口
Noriaki Tsukuda
憲明 築田
Hidenao Saito
秀直 斎藤
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.)
Rengo Co Ltd
Original Assignee
Rengo 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 Rengo Co Ltd filed Critical Rengo Co Ltd
Priority to JP2002098560A priority Critical patent/JP2003289781A/en
Publication of JP2003289781A publication Critical patent/JP2003289781A/en
Pending legal-status Critical Current

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  • Catching Or Destruction (AREA)
  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a vaporizing apparatus stably vaporizing a volatile chemical over a somewhat long period. <P>SOLUTION: The vaporizing apparatus is composed of a chemical composition-containing carrier and a fan. The chemical composition-containing carrier is arranged in an air stream produced with the fan. The chemical composition-containing carrier is obtained by mixing the volatile chemical with an embedding material so as to provide 0.1-50 ratio of the embedding material/ volatile chemical expressed in terms of weight ratio and supporting the resultant mixture on a granular carrier having 1-15 mm grain diameter. <P>COPYRIGHT: (C)2004,JPO

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】この発明は、薬剤組成物含有
担体及びファンから構成される揮散装置に関する。
TECHNICAL FIELD The present invention relates to a volatilization device comprising a carrier containing a pharmaceutical composition and a fan.

【0002】[0002]

【従来の技術】揮散性の殺虫剤を部屋内に揮散させる場
合、この薬剤の蒸気圧が低いために、ファンを利用して
揮散を促進させるものが、特開平8−147号公報や特
開平7−111850号公報に開示されている。
2. Description of the Related Art When a volatile insecticide is volatilized in a room, a fan is used to promote the volatilization because the vapor pressure of the chemical is low. It is disclosed in Japanese Patent Laid-Open No. 7-111850.

【0003】これらの技術は、上記薬剤を保持体に含浸
したもので、薬剤揮散量が偏らないようにハニカム構造
にしたり、その構造の穴径と保持体の奥行きを規定した
ものである。
In these techniques, a carrier is impregnated with the above-mentioned drug, and a honeycomb structure is formed so that the amount of the drug volatilized is not biased, and the hole diameter of the structure and the depth of the carrier are defined.

【0004】[0004]

【発明が解決しようとする課題】しかしながら、長期に
亘って薬剤を揮散させるためには、上記保持体の奥行を
長くしたり、構造を多くしなければならず、それに合わ
せてファンが大きくなり、装置が大型化してしまう。
However, in order to volatilize the drug over a long period of time, it is necessary to lengthen the depth of the holding body or increase the structure thereof, and the fan becomes larger accordingly. The device becomes large.

【0005】これに対し、粒状の薬剤含浸体を用いたも
のが、特開平10−191862号公報に開示されてい
る。上記薬剤含浸体は、粒状のため風が均一にあたり、
風の流れ方向の部位による揮散量のバラツキを解消する
ことができる。また、粒状なので、薬剤の担持量が多
く、装置をコンパクトにすることができる。
On the other hand, the one using a granular drug impregnated body is disclosed in Japanese Patent Application Laid-Open No. 10-191862. Since the chemical impregnated body is granular, the wind hits it uniformly,
It is possible to eliminate the variation in the amount of volatilization due to the part in the wind flow direction. Further, since it is granular, a large amount of the drug is carried, and the device can be made compact.

【0006】ところが、この技術は、薬剤を含浸させて
いるため、風が当たると薬剤含浸体間で薬剤移動が生
じ、初期の揮散速度が速く、その後、時間と共に急激に
揮散速度が低下する。また、薬剤の染み出し、べたつ
き、周囲を汚す等のおそれがある。
However, since this technique impregnates the chemicals, the chemicals move between the chemical-impregnated bodies when exposed to the air, and the initial volatilization rate is fast, and thereafter, the volatilization rate rapidly decreases with time. In addition, there is a risk of exudation of the drug, stickiness, and stains on the surroundings.

【0007】そこでこの発明は、揮散性薬剤をある程度
長期間にわたって安定して揮散させることができる揮散
装置を提供することを目的とする。
[0007] Therefore, an object of the present invention is to provide a volatilization device capable of stably volatilizing a volatile chemical for a certain period of time.

【0008】[0008]

【課題を解決するための手段】この発明は、薬剤組成物
含有担体及びファンから構成し、この薬剤組成物含有担
体を上記ファンによる気流内に配置したものであり、上
記薬剤組成物含有担体として、揮散性薬剤と包埋材と
を、重量比で包埋材/揮散性薬剤=0.1〜50となる
ように混合し、粒径1〜15mmの粒状担体に担持させ
ることにより上記の課題を解決したのである。
The present invention comprises a pharmaceutical composition-containing carrier and a fan, and the pharmaceutical composition-containing carrier is placed in an air stream by the fan, and is used as the pharmaceutical composition-containing carrier. The problem described above is obtained by mixing the volatile drug and the embedding material in a weight ratio of embedding material / volatile agent = 0.1 to 50 and supporting them on a granular carrier having a particle size of 1 to 15 mm. Is solved.

【0009】薬剤組成物含有担体として、所定の粒状担
体に担持させることで、風量が大きくても均一に担体に
風が当たり、揮散量のバラツキが発生しない。また、揮
散性薬剤と包埋材とを所定割合で混合することで、風の
影響によって担体間の薬剤の移動(偏り)が抑えられる
ため、ある程度長期間にわたって、揮散性薬剤を安定し
て揮散させることができる。さらに、包埋材の種類及び
量で揮散量を調整できる。
By loading a predetermined granular carrier as the drug composition-containing carrier, even if the air volume is large, the air is uniformly blown to the carrier and the volatilization amount does not vary. In addition, by mixing the volatile drug and the embedding material in a prescribed ratio, the migration (unevenness) of the drug between the carriers due to the influence of the wind can be suppressed, so that the volatile drug can be stably volatile for a certain period of time. Can be made. Furthermore, the volatilization amount can be adjusted by the type and amount of the embedding material.

【0010】[0010]

【発明の実施の形態】以下において、この発明について
詳細に説明する。この発明にかかる揮散装置は、図1に
示すように、薬剤組成物含有担体1及びファン2から構
成されるものである。この薬剤組成物含有担体1は、上
記ファン2によって生じる気流内、より好ましくは、上
記ファン2によって生じる風を直接受ける位置に配置さ
れる。これにより、薬剤組成物含有担体1から揮散した
揮散性薬剤がこの発明にかかる揮散装置の置かれる空間
内に拡散する。
BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in detail below. As shown in FIG. 1, the volatilization apparatus according to the present invention comprises a drug composition-containing carrier 1 and a fan 2. The pharmaceutical composition-containing carrier 1 is arranged in the air flow generated by the fan 2, more preferably at a position that directly receives the wind generated by the fan 2. As a result, the volatile drug that has volatilized from the drug composition-containing carrier 1 diffuses into the space in which the volatilization device according to the present invention is placed.

【0011】上記薬剤組成物含有担体1は、揮散性薬剤
と包埋材との混合物を、粒状担体に担持させたものであ
る。上記揮散性薬剤とは、常温あるいは加温した時に揮
散性を有するものをいう。このような揮散性薬剤として
は、芳香剤、抗菌・防カビ剤、殺虫剤、防虫剤等があげ
られる。これらは、揮散性薬剤の種類によって空間内に
おいて効果を発揮するのに有効な濃度が異なるため、目
的に応じて適当な揮散性薬剤を選定する。上記の芳香剤
や抗菌・防カビ剤の蒸気圧は、特に限定されないが、1
〜1000mmHgが好ましい。1000mmHgより
大きいと、揮散速度が速すぎるため、揮散速度を安定に
制御しきれないときがある。一方、1mmHg未満で
は、十分な有効濃度に達しないときがある。
The carrier 1 containing the drug composition is a granular carrier carrying a mixture of a volatile drug and an embedding material. The above-mentioned volatile chemical means a chemical that is volatile when heated at room temperature or heated. Examples of such volatile agents include aromatic agents, antibacterial / antifungal agents, insecticides, insecticides and the like. Since the effective concentration of these is effective for exerting the effect in the space depending on the type of the volatile drug, an appropriate volatile drug is selected according to the purpose. The vapor pressure of the above fragrance or antibacterial / antifungal agent is not particularly limited,
~ 1000 mmHg is preferred. If it is more than 1000 mmHg, the volatilization rate is too fast, and the volatilization rate may not be controlled stably. On the other hand, if it is less than 1 mmHg, a sufficient effective concentration may not be reached.

【0012】また、上記の殺虫剤や防虫剤の蒸気圧は、
特に限定されないが、上記と同じ理由で0.00001
〜0.01mmHgが好ましい。
The vapor pressures of the above insecticides and insect repellents are
Although not particularly limited, it is 0.00001 for the same reason as above.
~ 0.01 mmHg is preferred.

【0013】上記芳香剤としては、天然芳香剤や合成芳
香剤等があげられる。さらに、上記抗菌・防カビ剤とし
ては、アリルイソチオシアネート、オイゲノール、ヒノ
キチオール等があげられる。また、上記防虫剤として
は、ピレトリン、アレスレン、ペルメトリン等があげら
れる。上記殺虫剤としては、エンペンスリン、ベンフル
スリン、フェンフルスリン等のピレスロイド系防虫剤が
あげられる。
Examples of the fragrance include natural fragrance and synthetic fragrance. Further, examples of the antibacterial / antifungal agent include allyl isothiocyanate, eugenol, hinokitiol and the like. Examples of the insect repellent include pyrethrin, allethrene, permethrin and the like. Examples of the insecticide include pyrethroid insect repellents such as empensulin, benfluthrin, and fenfluthrin.

【0014】上記包埋材とは、常温時に固体で、上記揮
散性薬剤と混練可能であるものをいい、目的とする揮散
性薬剤の種類と有効な揮散量に応じ適宜選ばれる。上記
包埋材の例としては、オゾケライトに代表される鉱物ワ
ックス、パラフィンワックスやマイクロクリスタリンワ
ックス等の石油ワックス、脂肪酸やカルナバワックス、
ライスワックス等の天然ワックス、ガムロジン、ウッド
ロジン、トール油ロジンや変性ロジン及びそのエステル
化物、又は、ステアリルアルコール、ステアリン酸アミ
ド、安息香酸、2,6−ジ−t−ブチル−4−メチルフ
ェノール等があげられる。これらは、単独で使用するこ
とができ、また、2種以上を混合して使用することがで
きる。
The above-mentioned embedding material refers to a material which is solid at room temperature and can be kneaded with the volatile drug, and is appropriately selected depending on the kind of the volatile drug and the effective volatile amount. Examples of the embedding material include mineral wax represented by ozokerite, petroleum wax such as paraffin wax and microcrystalline wax, fatty acid and carnauba wax,
Natural wax such as rice wax, gum rosin, wood rosin, tall oil rosin, modified rosin and esterified products thereof, stearyl alcohol, stearic acid amide, benzoic acid, 2,6-di-t-butyl-4-methylphenol, etc. can give. These can be used alone or in combination of two or more.

【0015】上記揮散性薬剤と包埋材との混合比は、目
的とする揮散性薬剤の種類と有効な揮散量に応じて選択
し、重量比で包埋材/揮散性薬剤=0.1〜50がよ
く、0.5〜3が好ましい。0.1より小さいと、包埋
材の量が十分でないため、風量が大きくなると揮散性薬
剤の担体間の移動が生じて、長期間に亘り一定の揮散量
を確保することが困難となる。一方、50を超えると、
粒状担体が必要以上に多くなり、揮散装置が大型化す
る。
The mixing ratio of the volatile drug and the embedding medium is selected according to the kind of the volatile drug of interest and the effective amount of volatilization, and the weight ratio of embedding medium / volatilizing drug = 0.1. -50 is preferable, and 0.5-3 is preferable. If it is less than 0.1, the amount of the embedding material is not sufficient. Therefore, if the air volume becomes large, the volatile drug moves between the carriers, and it becomes difficult to secure a constant volatile amount for a long period of time. On the other hand, when it exceeds 50,
The number of granular carriers increases more than necessary, and the volatilization device becomes large.

【0016】上記粒状担体とは、上記の揮散性薬剤と包
埋材との混合物を担持することができ、かつ揮散性薬剤
との反応性に乏しい粒状物をいう。この担体を構成する
材質としては、セルロース、キトサン等の天然高分子及
びそれらの誘導体、ポリビニルアルコール、ポリウレタ
ン、ポリエチレン、ポリプロピレン等の合成高分子、ケ
イ酸塩、シリカゲル、ゼオライト、アルミナ等の無機化
合物等があげられる。
The above-mentioned granular carrier means a granular substance which can carry the mixture of the volatile drug and the embedding material and has a poor reactivity with the volatile drug. Examples of the material forming the carrier include natural polymers such as cellulose and chitosan and their derivatives, synthetic polymers such as polyvinyl alcohol, polyurethane, polyethylene and polypropylene, inorganic compounds such as silicates, silica gel, zeolite and alumina. Can be given.

【0017】また、上記粒状担体の粒径は、1〜15m
mがよく、2〜8mmが好ましい。1mmより小さい
と、圧力損失が生じて粒状担体に均一に風が当たらな
い。一方、15mmより大きいと、風が粒状担体に当た
らずに素通りする。
The particle size of the granular carrier is 1 to 15 m.
m is good, and 2-8 mm is preferable. If it is less than 1 mm, a pressure loss occurs and the granular carrier is not uniformly blown. On the other hand, if it is larger than 15 mm, the wind passes through the granular carrier without hitting it.

【0018】上記薬剤組成物含有担体1は、図1に示す
ように、ファン2の気流内に配置されるが、この薬剤組
成物含有担体1の収納部3のうち、上記気流の流れ方向
に対向する面は、この気流が通り抜けることができるよ
うな通気性部材4で構成されることが好ましい。この通
気性部材4としては、メッシュ、格子等を有する部材が
あげられる。
As shown in FIG. 1, the drug composition-containing carrier 1 is arranged in the air flow of the fan 2. In the accommodating portion 3 of the drug composition-containing carrier 1, the drug composition-containing carrier 1 is arranged in the flow direction of the air flow. The opposing surfaces are preferably made of breathable member 4 that allows the airflow to pass through. The breathable member 4 may be a member having a mesh, a lattice, or the like.

【0019】[0019]

【実施例】以下に実施例及び比較例をあげてこの発明を
さらに具体的に説明する。まず、実施例及び比較例にお
いて用いた薬品、及び試験方法を次に記載する。 <薬品> (1)揮散性薬剤 ・エンペンスリン:住友化学工業(株)製(以下、「E
PT」と略する。) ・シトラス香料:高砂香料(株)製;シトラス (2)包埋材 ・ステアリルアルコール:花王(株)製;カルコール8
098 ・ロジンエステル:荒川化学(株)製;AA−G
EXAMPLES The present invention will be described more specifically with reference to Examples and Comparative Examples below. First, the chemicals used in Examples and Comparative Examples and the test method are described below. <Chemicals> (1) Volatile chemicals and empensulin: manufactured by Sumitomo Chemical Co., Ltd. (hereinafter referred to as “E
Abbreviated as "PT". ) ・ Citrus fragrance: Takasago Fragrance Co., Ltd .; Citrus (2) embedding material ・ Stearyl alcohol: Kao Co., Ltd .; CALCOL 8
098 ・ Rosin ester: Arakawa Chemical Co., Ltd .; AA-G

【0020】(実施例1〜4、比較例1〜2)表1に記
載の揮散性薬剤及び包埋材を表1に記載の割合で混合
し、これを粒状担体としてセルロースビーズ(レンゴー
(株)製:ビスコパール、粒径は表1に示す。)4gに
揮散性薬剤としてEPT100mgを担持させ、薬剤組
成物含有担体を製造した。この薬剤組成物含有担体40
mlを対向する両端面が通気性部分であるワリフ(日石
プラスト(株)製:HS−24)で形成された円筒容器
(5cmφ×3cm)に充填し、シロッコファンの排気
口に取り付けた。回転開始から1ヶ月後(初期)、回転
開始から2ヶ月経過後(中期)、回転開始から3ヶ月経
過後(後期)の薬剤組成物含有担体中の残存薬剤量をガ
スクロマトグラフィーによって分析し、薬剤減少量を1
ヶ月間の揮散量とした。その結果を表1に示す。
(Examples 1 to 4 and Comparative Examples 1 and 2) Volatile drugs and embedding materials shown in Table 1 were mixed in the proportions shown in Table 1, and this was used as a granular carrier for cellulose beads (RENGO (stock). ): Viscopearl, particle size is shown in Table 1.) 4 g was loaded with 100 mg of EPT as a volatile drug to manufacture a drug composition-containing carrier. Carrier 40 containing this pharmaceutical composition
ml was filled in a cylindrical container (5 cmφ × 3 cm) made of a wallif (HS-24, manufactured by Nisseki Plast Co., Ltd.) having opposing air-permeable parts, and attached to the exhaust port of a sirocco fan. 1 month after the start of rotation (initial), 2 months after the start of rotation (middle period), and 3 months after the start of rotation (latter period), the amount of residual drug in the drug composition-containing carrier is analyzed by gas chromatography, Drug reduction amount is 1
It was the amount of volatilization for a month. The results are shown in Table 1.

【0021】[0021]

【表1】 [Table 1]

【0022】(比較例3)実施例2のうち、包埋材とし
てステアリルアルコールの重量を50g(包埋材/揮散
性薬剤=500)とした。しかし、薬剤組成物含有担体
が150mlとなってしまい、上記円筒容器にその全量
を充填し得なかった。
Comparative Example 3 In Example 2, the weight of stearyl alcohol as the embedding material was 50 g (embedding material / volatile agent = 500). However, the carrier containing the pharmaceutical composition was 150 ml, and the entire amount could not be filled in the cylindrical container.

【0023】[0023]

【発明の効果】この発明によれば、薬剤組成物含有担体
として、所定の粒状担体に担持させるので、風量が大き
くても均一に担体に風が当たり、揮散量のバラツキが発
生しない。
EFFECTS OF THE INVENTION According to the present invention, as a carrier for containing a pharmaceutical composition, it is supported on a predetermined granular carrier, so that even if the air volume is large, the air is uniformly blown to the carrier and the volatilization amount does not vary.

【0024】また、揮散性薬剤と包埋材とを所定割合で
混合するので、風の影響によって担体間の薬剤の移動
(偏り)が抑えられるため、ある程度長期間にわたっ
て、揮散性薬剤を安定して揮散させることができる。さ
らに、包埋材の種類及び量で揮散量を調整できる。
Further, since the volatile drug and the embedding material are mixed at a predetermined ratio, the migration (bias) of the drug between the carriers can be suppressed by the influence of the wind, so that the volatile drug can be stabilized for a certain period of time. Can be volatilized. Furthermore, the volatilization amount can be adjusted by the type and amount of the embedding material.

【図面の簡単な説明】[Brief description of drawings]

【図1】この発明にかかる揮散装置の例を示す模式図FIG. 1 is a schematic diagram showing an example of a volatilization device according to the present invention.

【符号の説明】[Explanation of symbols]

1 薬剤組成物含有担体 2 ファン 3 収納部 4 通気性部材 1 Pharmaceutical composition-containing carrier 2 fans 3 storage 4 Breathable material

───────────────────────────────────────────────────── フロントページの続き (72)発明者 斎藤 秀直 福井県坂井郡金津町自由ケ丘1丁目8番10 号 レンゴー株式会社福井研究所内 Fターム(参考) 2B121 AA11 AA20 CA02 CA15 CA43 CA44 CA61 CC02 CC03 CC04 EA01 FA05 4C002 AA03 BB02 DD03 DD06 FF01 HH06 KK01    ─────────────────────────────────────────────────── ─── Continued front page    (72) Inventor Hidenao Saito             1-8-10 Jiyugaoka, Kanazu-cho, Sakai-gun, Fukui Prefecture             No. Rengo Co., Ltd. Fukui Research Center F term (reference) 2B121 AA11 AA20 CA02 CA15 CA43                       CA44 CA61 CC02 CC03 CC04                       EA01 FA05                 4C002 AA03 BB02 DD03 DD06 FF01                       HH06 KK01

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 薬剤組成物含有担体及びファンから構成
し、この薬剤組成物含有担体を上記ファンによる気流内
に配置したものであり、上記薬剤組成物含有担体とし
て、揮散性薬剤と包埋材とを、重量比で包埋材/揮散性
薬剤=0.1〜50となるように混合し、粒径1〜15
mmの粒状担体に担持させたものを用いた揮散装置。
1. A drug composition-containing carrier and a fan, wherein the drug composition-containing carrier is placed in an air stream by the fan, and the volatile drug and the embedding material are used as the drug composition-containing carrier. And are mixed in a weight ratio of embedding material / volatile agent = 0.1 to 50 to obtain a particle size of 1 to 15
A volatilization device using what was supported on a granular carrier of mm.
【請求項2】 上記揮散性薬剤が常温又は加温時に揮散
性を有する芳香剤、抗菌・防カビ剤、防虫剤又は殺虫剤
である請求項1に記載の揮散装置。
2. The volatilization apparatus according to claim 1, wherein the volatile chemical is a fragrance, an antibacterial / antifungal agent, an insect repellent or an insecticide which has volatility at room temperature or when heated.
JP2002098560A 2002-04-01 2002-04-01 Vaporizing apparatus Pending JP2003289781A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2002098560A JP2003289781A (en) 2002-04-01 2002-04-01 Vaporizing apparatus

Publications (1)

Publication Number Publication Date
JP2003289781A true JP2003289781A (en) 2003-10-14

Family

ID=29240501

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005160469A (en) * 2003-11-10 2005-06-23 Dainippon Jochugiku Co Ltd Chemical-volatilizing device
JP2016019642A (en) * 2014-07-15 2016-02-04 株式会社Clox Air cleaning apparatus
JP2021153971A (en) * 2020-03-27 2021-10-07 東洋製罐グループホールディングス株式会社 Aromatic composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005160469A (en) * 2003-11-10 2005-06-23 Dainippon Jochugiku Co Ltd Chemical-volatilizing device
JP2016019642A (en) * 2014-07-15 2016-02-04 株式会社Clox Air cleaning apparatus
JP2021153971A (en) * 2020-03-27 2021-10-07 東洋製罐グループホールディングス株式会社 Aromatic composition
JP7496053B2 (en) 2020-03-27 2024-06-06 東洋製罐グループホールディングス株式会社 Fragrance composition

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