JPH06247811A - Insecticidal composition - Google Patents

Insecticidal composition

Info

Publication number
JPH06247811A
JPH06247811A JP5031700A JP3170093A JPH06247811A JP H06247811 A JPH06247811 A JP H06247811A JP 5031700 A JP5031700 A JP 5031700A JP 3170093 A JP3170093 A JP 3170093A JP H06247811 A JPH06247811 A JP H06247811A
Authority
JP
Japan
Prior art keywords
average particle
composition
particle size
insecticidal
fenobucarb
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.)
Granted
Application number
JP5031700A
Other languages
Japanese (ja)
Other versions
JP3269160B2 (en
Inventor
Toshiro Otsubo
敏朗 大坪
Yoshikazu Murakami
美和 村上
Isato Tejima
勇人 手嶋
Seiji Inai
誠二 井内
Masao Ogawa
雅男 小川
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP03170093A priority Critical patent/JP3269160B2/en
Priority to TW83100719A priority patent/TW307662B/zh
Priority to MYPI94000358A priority patent/MY110689A/en
Priority to MX9401266A priority patent/MX9401266A/en
Priority to CO94006721A priority patent/CO4290469A1/en
Publication of JPH06247811A publication Critical patent/JPH06247811A/en
Application granted granted Critical
Publication of JP3269160B2 publication Critical patent/JP3269160B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To obtain an insecticidal composition maintaining the insecticidal effect over a long period, especially effective for controlling wood injurious insects, etc., and reduced in toxicity. CONSTITUTION:A microcapsuled insecticidal composition comprising a carbamate insecticidal compound such as fenobucarb, propoxur, xylylcarb, metolcarb, isoprocarb or metoxadiazone capsuled with coating films having an average particle diameter of 5-80mum and an average particle diameter/film thickness of <200, and suitable for controlling wood injurious insects.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は殺虫組成物に関するもの
である。さらに詳しく述べると、特に木材害虫を防除す
るために適した殺虫組成物に関するものである。
This invention relates to insecticidal compositions. More particularly, it relates to an insecticidal composition suitable for controlling wood pests.

【従来の技術および発明が解決しようとする課題】従
来、木材害虫を防除するための殺虫組成物が種々知られ
ているが、木材害虫防除においては、安価で長期間の残
効性のあることが必要とされ、かつ、以前盛んに用いら
れていた有機塩素系殺虫剤のような残留毒性による問題
のないものが求められており、こうした諸条件を満たす
有効な殺虫組成物の開発が望まれていた。
2. Description of the Related Art Conventionally, various insecticidal compositions for controlling wood pests are known, but they are inexpensive and have a long-term residual effect in controlling wood pests. In addition, there is a need for compounds that do not have problems due to residual toxicity, such as organochlorine insecticides that have been used extensively in the past, and the development of effective insecticidal compositions that satisfy these conditions is desired. Was there.

【0002】[0002]

【課題を解決するための手段】カーバメート系殺虫化合
物は、一般に安価であるが、白蟻、ヒラタキクイムシ等
の木材害虫防除に用いるには、長期間の残効性を付与
し、かつ残留毒性による問題がないように工夫する必要
がある。本発明は、平均粒径が5〜80μm、好ましく
は10〜80μmであり、(平均粒径/膜厚)値が20
0未満、好ましくは100未満である被膜中に、カーバ
メート系殺虫化合物が内包されてなるマイクロカプセル
化された殺虫組成物(以下、本発明組成物と記す。)を
提供するものであり、本発明組成物は木材害虫を防除す
るのに特に適したものである。
[Means for Solving the Problems] Carbamate insecticidal compounds are generally inexpensive, but when used for controlling wood pests such as termites and flat beetles, they impart a long-term residual effect and are a problem due to residual toxicity. It is necessary to devise so that there is not. In the present invention, the average particle size is 5 to 80 μm, preferably 10 to 80 μm, and the (average particle size / film thickness) value is 20.
The present invention provides a microencapsulated insecticidal composition (hereinafter referred to as the composition of the present invention) in which a carbamate insecticidal compound is included in a coating film having a coating amount of less than 0, preferably less than 100. The composition is particularly suitable for controlling wood pests.

【0003】本発明において用いられるカーバメート系
殺虫化合物は特に限定されないが、例えば以下に示す化
合物が挙げられる。 フェノブカルブ;2−セカンダリーブチルフェニル N
−メチルカーバメート プロポキスル;2−イソプロポキシフェニル N−メチ
ルカーバメート キシリルカルブ;3,4−キシリル N−メチルカーバ
メート メトルカルブ;m−トリル N−メチルカーバメート イソプロカルブ;2−イソプロピルフェニル N−メチ
ルカーバメート メトキサジアゾン;5−メトキシ−3−(2−メトキシ
フェニル)−1,3,4−オキサジアゾール−2(3
H)−オン 尚、本発明でいうカーバメート系殺虫化合物とは、上記
したメトキサジアゾンのような環状のカーバメート系殺
虫化合物をも含むものである。
The carbamate insecticidal compound used in the present invention is not particularly limited, but examples thereof include the compounds shown below. Fenobucarb; 2-Secondary butylphenyl N
-Methylcarbamate propoxur; 2-isopropoxyphenyl N-methylcarbamate xylylcarb; 3,4-xylyl N-methylcarbamate metolcarb; m-tolyl N-methylcarbamate isoprocarb; 2-isopropylphenyl N-methylcarbamate methoxadiazone; 5-methoxy- 3- (2-methoxyphenyl) -1,3,4-oxadiazole-2 (3
H) -one In addition, the carbamate-based insecticidal compound in the present invention includes a cyclic carbamate-based insecticidal compound such as methoxadiazone described above.

【0004】殺虫化合物をマイクロカプセル化する方法
は種々知られているが、例えば特開昭62−21550
4号公報、特開昭62−215505号公報、特開昭6
3−22004号公報等に記載の界面重合法を用いるの
が簡便で、しかも目的の平均粒径、(平均粒径/膜厚)
値が得られるようにマイクロカプセル化反応を制御し易
い。該マイクロカプセルの膜物質としては、ポリウレタ
ン、ポリウレア、ポリアミド、ポリエステル、ポリカー
ボナート、ポリスルホナート、ポリスルホンアミド等が
挙げられる。
Various methods for microencapsulating an insecticidal compound are known, for example, JP-A-62-21550.
4, JP-A-62-215505 and JP-A-6-215505.
It is simple to use the interfacial polymerization method described in JP-A-3-22004, and the desired average particle size is (average particle size / film thickness).
It is easy to control the microencapsulation reaction so that a value can be obtained. Examples of the membrane material of the microcapsule include polyurethane, polyurea, polyamide, polyester, polycarbonate, polysulfonate, polysulfonamide and the like.

【0005】界面重合法を用いたポリウレア膜およびポ
リウレタン膜マイクロカプセルの製造法の一つを例に挙
げて、より詳しく説明すると以下の通りである。カーバ
メート系殺虫化合物と多価イソシアナートとを、必要に
よりフェニルキシリルエタン、メチルナフタレン等の溶
媒を加えて混合し、得られた油相を、分散剤を含有する
水相中に注入、攪拌しながら加熱してポリウレア膜を形
成させる。加熱する前または油相を水相中に注入する前
に、水相中に多価アルコールを添加しておくことによ
り、ポリウレタン膜を形成させることもできる。上述の
界面重合法による膜形成反応は、通常40〜80℃の範
囲内の温度で1時間以上、好ましくは1〜48時間かけ
て行われる。得られたスラリーをそのまま本発明組成物
として用いることもできるが、より使用し易くかつ安定
な形態に製剤化するのが良い。
A more detailed description will be given by taking one of the methods for producing microcapsules of a polyurea film and a polyurethane film using the interfacial polymerization method as an example. Carbamate insecticidal compounds and polyisocyanates are mixed by adding solvents such as phenylxylylethane and methylnaphthalene, if necessary, and the resulting oil phase is poured into an aqueous phase containing a dispersant and stirred. While heating, a polyurea film is formed. It is also possible to form a polyurethane film by adding a polyhydric alcohol to the water phase before heating or before injecting the oil phase into the water phase. The film-forming reaction by the above-mentioned interfacial polymerization method is usually carried out at a temperature within the range of 40 to 80 ° C. for 1 hour or longer, preferably 1 to 48 hours. The obtained slurry can be used as it is as the composition of the present invention, but it is better to formulate it into a stable form which is easier to use.

【0006】具体的な製剤形態としては、水性懸濁剤、
粉剤、水和剤、粒剤等、好ましくは水性懸濁剤が挙げら
れる。水性懸濁剤は、上記で得られたスラリーに増粘
剤、凍結防止剤、防腐剤、比重調節剤等の安定剤を添加
して製造される。増粘剤としては、例えばザンタンガ
ム、ラムザンガム、ローカストビーンガム、カラギーナ
ン、ウェランガム等の天然多糖類、ポリアクリル酸ソー
ダ塩等の合成高分子類、カルボキシメチルセルロース等
の半合成高分子類、アルミニウムマグネシウムシリケー
ト、スメクタイト、ベントナイト、ヘクトライト、乾式
法シリカ等の鉱物質微粉末、アルミナゾルなどの水中で
増粘効果のある物質が挙げられる。増粘剤の添加量は、
その種類等にもよるが、一般に本発明組成物100重量
部中に10重量部以下である。また、凍結防止剤として
は、例えばプロピレングリコール等が挙げられる。凍結
防止剤の添加量は、一般に本発明組成物100重量部中
に20重量部以下である。防腐剤としては、例えばパラ
ヒドロキシ安息香酸エステル、サリチル酸誘導体などの
通常の殺虫製剤に用いられるものが挙げられ、比重調節
剤としては、例えば硫酸ナトリウム等の水溶性塩類、尿
素等の水溶性肥料などが挙げられる。本発明組成物中の
カーバメート系殺虫化合物の含量は、その製剤形態によ
り異なるが一般に0.5〜80重量%であり、特に水性
懸濁剤の場合、通常0.5〜50重量%である。
[0006] As a specific formulation form, an aqueous suspension,
Powders, wettable powders, granules and the like, preferably aqueous suspensions are mentioned. The aqueous suspension is produced by adding a stabilizer such as a thickener, an antifreezing agent, an antiseptic and a specific gravity adjusting agent to the slurry obtained above. Examples of the thickener include xanthan gum, rhamsan gum, locust bean gum, carrageenan, natural polysaccharides such as welan gum, synthetic polymers such as polyacrylic acid sodium salt, semi-synthetic polymers such as carboxymethyl cellulose, aluminum magnesium silicate, and the like. Examples thereof include fine powders of mineral substances such as smectite, bentonite, hectorite and dry process silica, and substances having a thickening effect in water such as alumina sol. The amount of thickener added is
The amount is generally 10 parts by weight or less based on 100 parts by weight of the composition of the present invention, although it depends on the kind and the like. Examples of the antifreezing agent include propylene glycol and the like. The addition amount of the antifreezing agent is generally 20 parts by weight or less based on 100 parts by weight of the composition of the present invention. Examples of the antiseptic include those used in ordinary insecticidal preparations such as parahydroxybenzoic acid ester and salicylic acid derivatives, and examples of the specific gravity adjusting agent include water-soluble salts such as sodium sulfate and water-soluble fertilizers such as urea. Is mentioned. The content of the carbamate insecticidal compound in the composition of the present invention varies depending on the formulation form, but is generally 0.5 to 80% by weight, and particularly 0.5 to 50% by weight in the case of an aqueous suspension.

【0007】本発明組成物は、マイクロカプセルの平均
粒径が5〜80μmであり、(平均粒径/膜厚)値が2
00未満であるが、該平均粒径は、例えばコールターカ
ウンターTA−II型(コールターエレクトロニクス社
製、日科機取扱品)を用いて測定できる。また、膜厚は
以下の数式で計算するのが簡便である。
The composition of the present invention has an average particle size of microcapsules of 5 to 80 μm and an (average particle size / film thickness) value of 2
Although it is less than 00, the average particle diameter can be measured by using, for example, Coulter Counter TA-II type (manufactured by Coulter Electronics Co., Ltd., Nikkaki handling product). Further, it is easy to calculate the film thickness by the following formula.

【数1】 ここで、Dはマイクロカプセルの平均粒径、WW は膜物
質重量、WC は芯物質重量、ρW は膜物質密度、ρC
芯物質密度を表す。
[Equation 1] Here, D is the average particle size of the microcapsules, W W is the weight of the membrane substance, W C is the weight of the core substance, ρ W is the density of the membrane substance, and ρ C is the density of the core substance.

【0008】本発明組成物はシロアリ、ヒラタキクイム
シ等の木材害虫防除に特に有用であり、シロアリ防除に
用いられる場合、例えば本発明組成物またはその希釈液
を有効成分量で5〜50g/m2 程度、家屋の床下土壌
またはコンクリート表面等に散布する。あるいは、木部
処理に用いられる場合は例えば有効成分量で1〜5g/
2 程度を木部表面に処理する。ヒラタキクイムシ防除
に用いられる場合、例えば防虫合板としての使用が挙げ
られる。防虫合板製造の具体例としては、合板1m3
りの本発明組成物が有効成分量で10〜1000g程度となる
よう接着剤中に混入して板接着用糊を調製し、この糊を
用いて単板を貼合し、適温で加圧して防虫合板を得る方
法が挙げられる。用いられる接着剤としては、尿素樹脂
系、メラミン尿素系、変性フェノール樹脂系、アルカリ
フェノール樹脂系等の接着剤が挙げられる。また、本発
明組成物は木材害虫に限らず、アリ、カマドウマ、ゲジ
ゲジ、ムカデ、ワラジムシ、ダンゴムシ等の不快害虫の
防除にも有効である。この場合、例えば本発明組成物ま
たはその希釈液を有効成分量で1〜50g/m2 程度、
不快害虫にまたは不快害虫の生息場所に処理すればよ
い。
The composition of the present invention is particularly useful for controlling wood pests such as termites and flat beetles. When used for controlling termites, for example, the composition of the present invention or a diluted solution thereof is contained in an amount of 5 to 50 g / m 2 as an active ingredient. Disperse the soil under the floor of the house or concrete surface. Alternatively, when used for xylem treatment, for example, the amount of active ingredient is 1 to 5 g /
About 2 m 2 is treated on the wood surface. When it is used for the control of flat beetle, it may be used as, for example, an insect-control plywood. As a specific example of the production of insect-repellent plywood, the composition of the present invention is mixed in an adhesive so that the amount of the active ingredient is about 10 to 1000 g per 1 m 3 of plywood to prepare a paste for plate adhesion, and this paste is used. A method for obtaining a pest control plywood by laminating a single plate and pressurizing at a suitable temperature can be mentioned. Examples of the adhesive used include urea resin adhesives, melamine urea adhesives, modified phenolic resin adhesives, and alkali phenolic resin adhesives. Further, the composition of the present invention is effective not only for controlling wood pests but also for controlling unpleasant pests such as ants, horsetails, gudgeages, centipedes, wallworms, and pill bugs. In this case, for example, the composition of the present invention or a diluted solution thereof is contained in an amount of the active ingredient of about 1 to 50 g / m 2 ,
It can be applied to unpleasant pests or habitats of unpleasant pests.

【0009】[0009]

【実施例】次に、本発明を製造例、比較例、試験例を挙
げてより詳細に説明する。 製造例1 スミジュールL−75(住友バイエルウレタン社製芳香
族イソシアナート)40gとフェニルキシリルエタン1
50gとをフェノブカルブ150gに混合して均一にし
た後、これを17.5gのアラビアガムと20gのエチ
レングリコールとを含む水溶液400gに加え、T.K.オ
ートホモミクサー(特殊機化工業社製ホモジナイザー)
を用いて常温で攪拌分散し(回転速度; 5500rpm)、微
小滴を得た。次いで、60℃で24時間ゆるやかに攪拌
し、フェノブカルブがポリウレタン膜中に内包されたマ
イクロカプセルスラリーを得た。得られたスラリーに1
gのザンタンガムと5gのアルミニウムマグネシウムシ
リケートとを含む水溶液260gを加え、15重量%の
フェノブカルブを含む本発明組成物(1)を得た。得ら
れたマイクロカプセルの平均粒径は23.1μm、(平
均粒径/膜厚)値は70であった。
EXAMPLES Next, the present invention will be described in more detail with reference to production examples, comparative examples and test examples. Production Example 1 Sumidur L-75 (Sumitomo Bayer Urethane Co., Ltd. aromatic isocyanate) 40 g and phenylxylylethane 1
After mixing 50 g with 150 g of Fenobucarb to make it uniform, add this to 400 g of an aqueous solution containing 17.5 g of gum arabic and 20 g of ethylene glycol, and add TK auto homomixer (homogenizer manufactured by Tokushu Kika Kogyo Co., Ltd.).
Was stirred and dispersed at room temperature (rotation speed: 5500 rpm) to obtain fine droplets. Then, the mixture was gently stirred at 60 ° C. for 24 hours to obtain a microcapsule slurry in which fenobucarb was encapsulated in a polyurethane film. 1 in the resulting slurry
260 g of an aqueous solution containing g of xanthan gum and 5 g of aluminum magnesium silicate was added to obtain a composition (1) of the present invention containing 15% by weight of fenocarb. The average particle size of the obtained microcapsules was 23.1 μm, and the (average particle size / film thickness) value was 70.

【0010】製造例2 スミジュールL−75を40gにかえて60g、1gの
ザンタンガムと5gのアルミニウムマグネシウムシリケ
ートとを含む水溶液を260gにかえて280g使用し
た以外は全て製造例1と同様の操作にて、15重量%の
フェノブカルブを含む本発明組成物(2)を得た。得ら
れたマイクロカプセルの平均粒径は19.4μm、(平
均粒径/膜厚)値は48であった。 製造例3 スミジュールL−75を40gにかえて80g、1gの
ザンタンガムと5gのアルミニウムマグネシウムシリケ
ートとを含む水溶液を260gにかえて220g使用し
た以外は全て製造例1と同様の操作にて、15重量%の
フェノブカルブを含む本発明組成物(3)を得た。得ら
れたマイクロカプセルの平均粒径は21.1μm、(平
均粒径/膜厚)値は36であった。
Production Example 2 The same procedure as in Production Example 1 was repeated except that 60 g of SUMIJUR L-75 was replaced with 40 g, and 280 g of an aqueous solution containing 1 g of xanthan gum and 5 g of aluminum magnesium silicate was replaced with 260 g. Thus, a composition (2) of the present invention containing 15% by weight of fenocarb was obtained. The average particle size of the obtained microcapsules was 19.4 μm, and the (average particle size / film thickness) value was 48. Production Example 3 The same procedure as in Production Example 1 except that 220 g of an aqueous solution containing 80 g of Sumidule L-75 instead of 40 g and 1 g of xanthan gum and 5 g of aluminum magnesium silicate was used instead of 260 g were used. The composition (3) of the present invention containing Fenobucarb by weight was obtained. The average particle size of the obtained microcapsules was 21.1 μm, and the (average particle size / film thickness) value was 36.

【0011】製造例4 スミジュールL−75 40gとフェニルキシリルエタ
ン150gとをフェノブカルブ150gに混合して均一
にした後、これを20gのゴーセノールGL−05(日
本合成化学工業社製ポリビニルアルコール)と25gの
エチレングリコールとを含む水溶液400gに加え、T.
K.オートホモミクサーを用いて常温で攪拌分散し(回転
速度; 3700rpm)、微小滴を得た。次いで、60℃で2
4時間ゆるやかに攪拌し、フェノブカルブがポリウレタ
ン膜中に内包されたマイクロカプセルスラリーを得た。
得られたスラリーに1gのザンタンガムと5gのアルミ
ニウムマグネシウムシリケートとを含む水溶液260g
を加え、15重量%のフェノブカルブを含む本発明組成
物(4)を得た。得られたマイクロカプセルの平均粒径
は8.1μm、(平均粒径/膜厚)値は70であった。
Production Example 4 40 g of Sumidule L-75 and 150 g of phenylxylylethane were mixed with 150 g of fenocarb to homogenize the mixture, and this was mixed with 20 g of Gohsenol GL-05 (polyvinyl alcohol manufactured by Nippon Synthetic Chemical Industry Co., Ltd.). Add to 400 g of an aqueous solution containing 25 g of ethylene glycol,
K. Auto homomixer was used to stir and disperse at room temperature (rotation speed: 3700 rpm) to obtain fine droplets. Then 2 at 60 ℃
The mixture was gently stirred for 4 hours to obtain a microcapsule slurry in which fenobucarb was encapsulated in a polyurethane film.
260 g of an aqueous solution containing 1 g of xanthan gum and 5 g of aluminum magnesium silicate in the obtained slurry.
Was added to obtain a composition (4) of the present invention containing 15% by weight of Fenobucarb. The average particle size of the obtained microcapsules was 8.1 μm, and the (average particle size / film thickness) value was 70.

【0012】製造例5 スミジュールL−75 20gとフェニルキシリルエタ
ン150gとをフェノブカルブ150gに混合して均一
にした後、これを15gのアラビアガムと20gのエチ
レングリコールとを含む水溶液400gに加え、T.K.オ
ートホモミクサーを用いて常温で攪拌分散し(回転速
度; 5500rpm)、微小滴を得た。次いで、60℃で24
時間ゆるやかに攪拌し、フェノブカルブがポリウレタン
膜中に内包されたマイクロカプセルスラリーを得た。得
られたスラリーに1gのザンタンガムと5gのアルミニ
ウムマグネシウムシリケートとを含む水溶液280gを
加え、15重量%のフェノブカルブを含む本発明組成物
(5)を得た。得られたマイクロカプセルの平均粒径は
31μm、(平均粒径/膜厚)値は141であった。
Preparation Example 5 20 g of Sumidule L-75 and 150 g of phenylxylylethane were mixed with 150 g of fenocarb to make them uniform, and this was added to 400 g of an aqueous solution containing 15 g of gum arabic and 20 g of ethylene glycol. Using TK Autohomomixer, the mixture was stirred and dispersed at room temperature (rotation speed: 5500 rpm) to obtain microdroplets. Then 24 at 60 ℃
The mixture was gently stirred for a time to obtain a microcapsule slurry in which Fenobucarb was encapsulated in a polyurethane film. 280 g of an aqueous solution containing 1 g of xanthan gum and 5 g of aluminum magnesium silicate was added to the obtained slurry to obtain a composition (5) of the present invention containing 15% by weight of fenocarb. The average particle size of the obtained microcapsules was 31 μm, and the (average particle size / film thickness) value was 141.

【0013】製造例6 アラビアガム17.5gにかえて15g、エチレングリ
コール20gにかえて25g使用した以外は全て製造例
1と同様の操作にて、15重量%のフェノブカルブを含
む本発明組成物(6)を得た。得られたマイクロカプセ
ルの平均粒径は47.7μm、(平均粒径/膜厚)値は
70であった。 製造例7 スミジュールL−75 40gにかえて20g、アラビ
アガム15gにかえて17.5g、1gのザンタンガム
と5gのアルミニウムマグネシウムシリケートとを含む
水溶液を260gにかえて280g使用した以外は全て
製造例1と同様の操作にて、15重量%のフェノブカル
ブを含む本発明組成物(7)を得た。得られたマイクロ
カプセルの平均粒径は21.5μm、(平均粒径/膜
厚)値は138であった。 製造例8 スミジュールL−75 40gを加熱溶融させたフェノ
ブカルブ150gに混合して均一にした後、これを1
7.5gのアラビアガムと30gのエチレングリコール
とを含む水溶液400gに加え、T.K.オートホモミクサ
ーを用いて常温で攪拌分散し(回転速度; 5500rpm)、
微小滴を得た。次いで、60℃で24時間ゆるやかに攪
拌し、フェノブカルブがポリウレタン膜中に内包された
マイクロカプセルスラリーを得た。得られたスラリーに
1gのザンタンガムと5gのアルミニウムマグネシウム
シリケートとを含む水溶液410gを加え、15重量%
のフェノブカルブを含む本発明組成物(8)を得た。得
られたマイクロカプセルの平均粒径は19.7μm、
(平均粒径/膜厚)値は35であった。
Production Example 6 A composition of the present invention containing 15% by weight of fenocarb was prepared by the same procedure as in Production Example 1 except that 15 g of gum arabic was used instead of 17.5 g and ethylene glycol 20 g was used instead of 25 g. 6) was obtained. The average particle size of the obtained microcapsules was 47.7 μm, and the (average particle size / film thickness) value was 70. Production Example 7 Sumidule L-75 20 g instead of 40 g, gum arabic 15 g instead of 17.5 g, 1 g of xanthan gum and 5 g of aluminum magnesium silicate were changed to 260 g and all were used except that 280 g was used. By the same operation as in 1, a composition (7) of the present invention containing 15% by weight of fenocarb was obtained. The average particle size of the obtained microcapsules was 21.5 μm, and the (average particle size / film thickness) value was 138. Production Example 8 40 g of Sumidule L-75 was mixed with 150 g of Fenobucarb which was heated and melted to make it uniform, and then 1
Add to 400 g of an aqueous solution containing 7.5 g of gum arabic and 30 g of ethylene glycol, stir and disperse at room temperature using a TK auto homomixer (rotation speed: 5500 rpm),
Microdroplets were obtained. Then, the mixture was gently stirred at 60 ° C. for 24 hours to obtain a microcapsule slurry in which fenobucarb was encapsulated in a polyurethane film. To the obtained slurry, 410 g of an aqueous solution containing 1 g of xanthan gum and 5 g of aluminum magnesium silicate was added, and 15% by weight was added.
The composition (8) of the present invention containing the Fenobucarb of The average particle size of the obtained microcapsules was 19.7 μm,
The (average particle size / film thickness) value was 35.

【0014】製造例9 スミジュールL−75 40gとフェニルキシリルエタ
ン150gとをフェノブカルブ150gに混合して均一
にした後、これを17.5gのアラビアガムを含む水溶
液400gに加え、T.K.オートホモミクサーを用いて常
温で攪拌分散し(回転速度; 5500rpm)、微小滴を得
た。次いで、60℃で24時間ゆるやかに攪拌し、フェ
ノブカルブがポリウレア膜中に内包されたマイクロカプ
セルスラリーを得た。得られたスラリーに1gのザンタ
ンガムと5gのアルミニウムマグネシウムシリケートと
を含む水溶液260gを加え、15重量%のフェノブカ
ルブを含む本発明組成物(9)を得た。得られたマイク
ロカプセルの平均粒径は21.3μm、(平均粒径/膜
厚)値は78であった。
Production Example 9 40 g of Sumidule L-75 and 150 g of phenylxylylethane were mixed with 150 g of Fenobucarb to make it uniform, and this was added to 400 g of an aqueous solution containing 17.5 g of gum arabic, and TK autohomomixer was added. Was stirred and dispersed at room temperature (rotation speed: 5500 rpm) to obtain fine droplets. Then, the mixture was gently stirred at 60 ° C. for 24 hours to obtain a microcapsule slurry in which fenobucarb was encapsulated in a polyurea film. 260 g of an aqueous solution containing 1 g of xanthan gum and 5 g of aluminum magnesium silicate was added to the obtained slurry to obtain a composition (9) of the present invention containing 15% by weight of fenocarb. The average particle size of the obtained microcapsules was 21.3 μm, and the (average particle size / film thickness) value was 78.

【0015】製造例10 スミジュールN−75(住友バイエルウレタン社製脂肪
族イソシアナート)50gとフェニルキシリルエタン1
50gとをフェノブカルブ150gに混合して均一にし
た後、これを17.5gのアラビアガムと20gのエチ
レングリコールとを含む水溶液400gに加え、T.K.オ
ートホモミクサーを用いて常温で攪拌分散し(回転速
度; 5400rpm)、微小滴を得た。次いで、60℃で24
時間ゆるやかに攪拌し、フェノブカルブがポリウレタン
膜中に内包されたマイクロカプセルスラリーを得た。得
られたスラリーに1gのザンタンガムと5gのアルミニ
ウムマグネシウムシリケートとを含む水溶液250gを
加え、15重量%のフェノブカルブを含む本発明組成物
(10)を得た。得られたマイクロカプセルの平均粒径
は20.8μm、(平均粒径/膜厚)値は69であっ
た。
Production Example 10 50 g of Sumidur N-75 (aliphatic isocyanate manufactured by Sumitomo Bayer Urethane Co.) and 1 of phenylxylylethane
After mixing 50 g with 150 g of Fenobucarb to make it uniform, add this to 400 g of an aqueous solution containing 17.5 g of gum arabic and 20 g of ethylene glycol, and stir-disperse at room temperature using a TK autohomomixer (rotation speed 5400 rpm), microdroplets were obtained. Then 24 at 60 ℃
The mixture was gently stirred for a time to obtain a microcapsule slurry in which Fenobucarb was encapsulated in a polyurethane film. To the resulting slurry, 250 g of an aqueous solution containing 1 g of xanthan gum and 5 g of aluminum magnesium silicate was added to obtain a composition (10) of the present invention containing 15% by weight of fenocarb. The average particle size of the obtained microcapsules was 20.8 μm, and the (average particle size / film thickness) value was 69.

【0016】製造例11 合板用尿素樹脂74.4重量部に、本発明組成物(2)
8.7重量部を加え、さらに小麦粉14.9重量部、2
0重量%塩化アンモニウム水1.8重量部、水0.2部
を加え、良く混合して接着用の糊を調製した。含水率
7.5重量%の単板3枚(18cm×18cm、厚さは2枚
が1.0mmで、中央に用いる1枚が2.5mm)を、上述
の糊を30.3cm×30.3cm当たり30g用いて貼合し、室温
で20分間冷圧(10kg/cm2 )を加え、解圧後30分
間放置し、さらに115〜125℃の熱圧(10kg/cm
2 )を90秒間加えて合板を製造した。この合板製造
時、フェノブカルブによる臭気は感じられなかった。
Production Example 11 The composition (2) of the present invention was added to 74.4 parts by weight of a urea resin for plywood.
8.7 parts by weight were added, and further 14.9 parts by weight of flour, 2
1.8 parts by weight of 0% by weight aqueous ammonium chloride and 0.2 parts by weight of water were added and mixed well to prepare an adhesive paste. 3 veneers with a moisture content of 7.5% by weight (18 cm x 18 cm, thickness 2 is 1.0 mm, one for the center is 2.5 mm), and the above-mentioned glue per 30.3 cm x 30.3 cm pasted with 30 g, 20 min cold pressed to (10kg / cm 2) was added at room temperature, allowed to stand After depressurization for 30 minutes, further 115 to 125 ° C. for hot pressing (10 kg / cm
2 ) was added for 90 seconds to produce plywood. At the time of manufacturing this plywood, no odor due to Fenobucarb was felt.

【0017】比較例1 スミジュールL−75を40gにかえて10g、1gの
ザンタンガムと5gのアルミニウムマグネシウムシリケ
ートとを含む水溶液を260gにかえて290g使用し
た以外は全て製造例1と同様の操作にて、15重量%の
フェノブカルブを含む比較組成物(1)を得た。得られ
たマイクロカプセルの平均粒径は23μm、(平均粒径
/膜厚)値は273であった。 比較例2 スミジュールL−75 40gとフェニルキシリルエタ
ン150gとをフェノブカルブ150gに混合して均一
にした後、これを40gのゴーセノールGL−05と2
5gのエチレングリコールとを含む水溶液400gに加
え、T.K.オートホモミクサーを用いて常温で攪拌分散し
(回転速度; 5000rpm)、微小滴を得た。次いで、60
℃で24時間ゆるやかに攪拌し、フェノブカルブがポリ
ウレタン膜中に内包されたマイクロカプセルスラリーを
得た。得られたスラリーに1gのザンタンガムと5gの
アルミニウムマグネシウムシリケートとを含む水溶液2
60gを加え、15重量%のフェノブカルブを含む比較
組成物(2)を得た。得られたマイクロカプセルの平均
粒径は2.7μm、(平均粒径/膜厚)値は71であっ
た。
Comparative Example 1 The same procedure as in Preparation Example 1 was repeated except that 40 g of Sumidule L-75 was replaced with 40 g, and 290 g of an aqueous solution containing 1 g of xanthan gum and 5 g of aluminum magnesium silicate was replaced with 260 g. Thus, a comparative composition (1) containing 15% by weight of Fenobucarb was obtained. The average particle size of the obtained microcapsules was 23 μm, and the (average particle size / film thickness) value was 273. Comparative Example 2 40 g of Sumidule L-75 and 150 g of phenylxylylethane were mixed with 150 g of Fenobucarb to homogenize it, and this was mixed with 40 g of Gohsenol GL-05 and 2
To 400 g of an aqueous solution containing 5 g of ethylene glycol was added, and the mixture was stirred and dispersed at room temperature using a TK Autohomomixer (rotation speed: 5000 rpm) to obtain microdroplets. Then 60
The mixture was gently stirred at 24 ° C. for 24 hours to obtain a microcapsule slurry in which Fenobucarb was encapsulated in a polyurethane film. Aqueous solution 2 containing 1 g of xanthan gum and 5 g of aluminum magnesium silicate in the obtained slurry.
60 g was added to obtain a comparative composition (2) containing 15% by weight of Fenobucarb. The average particle size of the obtained microcapsules was 2.7 μm, and the (average particle size / film thickness) value was 71.

【0018】試験例1 500gの土壌に下記表1記載の各々の組成物の1重量
%水希釈液を50g処理し、処理された土壌をシャーレ
に入れ、イエシロアリ職蟻20頭を放ち3日後に生死を
観察した。また、前記処理土壌を40℃の暗条件下で3
か月保存したものについても、同様にイエシロアリ職蟻
20頭を放ち3日後に生死を観察した。結果を表1に示
す。
Test Example 1 500 g of soil was treated with 50 g of a 1% by weight water-diluted solution of each composition shown in Table 1 below, the treated soil was placed in a petri dish, and 20 termite termite workers were released and 3 days later. Observed life and death. In addition, the treated soil under dark conditions of 40 ℃ 3
Similarly, for those stored for a month, 20 dead termite worker ants were similarly released, and life and death were observed 3 days later. The results are shown in Table 1.

【表1】 上表に示されるように、本発明組成物は長期間にわた
り、シロアリ防除に有効な組成物である。
[Table 1] As shown in the above table, the composition of the present invention is a composition effective for controlling termites over a long period of time.

【0019】試験例2 縦50cm、横50cm、深さ30cmの箱中に、土壌を深さ
が10cmになるようにしきつめ、本発明組成物(2)の
1重量%水希釈液を1.25リットル散布した。散布直
後および40℃で所定日数保存後に、各々箱中にイエシ
ロアリ職蟻100頭を放ち翌日に生死を観察した。結果
を表2に示す。
Test Example 2 A box having a length of 50 cm, a width of 50 cm, and a depth of 30 cm was filled with soil so that the soil had a depth of 10 cm. L sprayed. Immediately after spraying and after storage at 40 ° C. for a predetermined number of days, 100 termite termite worker ants were released in each box, and life or death was observed on the next day. The results are shown in Table 2.

【表2】 [Table 2]

【0020】試験例3 直径9cmのガラスシャーレ中に、下記表3記載の各々の
組成物の水希釈液を有効成分量が30mgとなるように処
理し、風乾した。該シャーレを40℃で2週間保存後、
ガスクロマトグラフィーにより、シャーレ中の残存有効
成分量を測定し残存率(%)を求めた。結果を表3に示
す。
Test Example 3 A glass petri dish having a diameter of 9 cm was treated with a water-diluted solution of each composition shown in Table 3 below so that the amount of active ingredient was 30 mg, and air-dried. After storing the dish at 40 ° C. for 2 weeks,
The residual ratio (%) was determined by measuring the amount of active ingredient remaining in the petri dish by gas chromatography. The results are shown in Table 3.

【表3】 [Table 3]

【0021】試験例4 下記表4記載の各々の組成物について、ICR系マウス
(雄)を用いて急性経口毒性を調べた。表4に、3000mg
/kgを投与した際の死亡率(%)を示す。
Test Example 4 With respect to each composition shown in Table 4 below, acute oral toxicity was examined using ICR mouse (male). In Table 4, 3000mg
The mortality rate (%) when administering / kg is shown.

【表4】 上表に示されるように、本発明組成物は毒性の軽減され
た組成物である。
[Table 4] As shown in the table above, the composition of the present invention has reduced toxicity.

【0022】試験例5 製造例11で得た防虫合板を8cm×5cmに切り、その上
に32個の穴を有するアルミニウム板を重ね、各穴にヒ
ラタキクイムシ幼虫を入れ、各穴を人工飼料で埋め、さ
らに、アルミニウム板上にもう1枚の製造例11で得た
防虫合板(8cm×5cm)を重ねた。2か月保存後に防虫
合板を調査したところ、羽化したヒラタキクイムシに食
い破られた形跡は全く認められなかった。
Test Example 5 The insect-repellent plywood obtained in Production Example 11 was cut into 8 cm × 5 cm pieces, an aluminum plate having 32 holes was stacked on the plywood plate, and the larva of Beetle beetle was put in each hole, and each hole was made with artificial feed. After burying, another insect-proof plywood (8 cm × 5 cm) obtained in Production Example 11 was placed on the aluminum plate. When the insect-repellent plywood was examined after storage for 2 months, no evidence of being bitten by the flaked flatworm was found.

【0023】[0023]

【発明の効果】本発明組成物は、長期間にわたり殺虫効
力を維持することのできる毒性の軽減された組成物であ
り、木材害虫等の防除に有効である。
INDUSTRIAL APPLICABILITY The composition of the present invention is a composition with reduced toxicity capable of maintaining insecticidal efficacy for a long period of time and is effective for controlling wood pests and the like.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 井内 誠二 兵庫県宝塚市高司4丁目2番1号 住友化 学工業株式会社内 (72)発明者 小川 雅男 兵庫県宝塚市高司4丁目2番1号 住友化 学工業株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Seiji Inouchi 4-2-1 Takashi, Takarazuka-shi, Hyogo Sumitomo Kagaku Kogyo Co., Ltd. (72) Inventor Masao Ogawa 4-2-1 Takashi, Takarazuka-shi, Hyogo Sumitomo Chemical Co., Ltd.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】平均粒径が5〜80μmであり、(平均粒
径/膜厚)値が200未満である被膜中に、カーバメー
ト系殺虫化合物が内包されてなることを特徴とするマイ
クロカプセル化された殺虫組成物。
1. A microencapsulation characterized in that a carbamate insecticidal compound is encapsulated in a film having an average particle size of 5 to 80 μm and an (average particle size / film thickness) value of less than 200. Insecticidal composition.
【請求項2】木材害虫を防除するための、請求項1記載
の殺虫組成物。
2. The insecticidal composition according to claim 1, for controlling wood pests.
【請求項3】カーバメート系殺虫化合物が、フェノブカ
ルブ、プロポキスル、キシリルカルブ、メトルカルブ、
イソプロカルブおよびメトキサジアゾンから選ばれる一
種以上であることを特徴とする請求項1または請求項2
記載の殺虫組成物。
3. A carbamate insecticidal compound is fenobucarb, propoxur, xylylcarb, metolcarb,
It is 1 or more types chosen from an isoprocarb and a methoxadiazone, Claim 1 or Claim 2 characterized by the above-mentioned.
The insecticidal composition described.
【請求項4】カーバメート系殺虫化合物がフェノブカル
ブであることを特徴とする請求項1または請求項2記載
の殺虫組成物。
4. The insecticidal composition according to claim 1, wherein the carbamate insecticidal compound is fenobucarb.
JP03170093A 1993-02-22 1993-02-22 Insecticidal composition Expired - Fee Related JP3269160B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP03170093A JP3269160B2 (en) 1993-02-22 1993-02-22 Insecticidal composition
TW83100719A TW307662B (en) 1993-02-22 1994-01-28
MYPI94000358A MY110689A (en) 1993-02-22 1994-02-17 Microencapsulated carbamate insecticidal composition and method for controlling insects
MX9401266A MX9401266A (en) 1993-02-22 1994-02-18 INSECTICIDE COMPOSITIONS.
CO94006721A CO4290469A1 (en) 1993-02-22 1994-02-22 INSECTICIDE COMPOSITION OF MICROENCAPSULATED CARBAMATE SUITABLE FOR CONTROLLING INSECTS THAT PERFORATE WOOD

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP03170093A JP3269160B2 (en) 1993-02-22 1993-02-22 Insecticidal composition

Publications (2)

Publication Number Publication Date
JPH06247811A true JPH06247811A (en) 1994-09-06
JP3269160B2 JP3269160B2 (en) 2002-03-25

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ID=12338353

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JP03170093A Expired - Fee Related JP3269160B2 (en) 1993-02-22 1993-02-22 Insecticidal composition

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Country Link
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107047557A (en) * 2016-12-14 2017-08-18 安徽东健化工科技有限公司 A kind of microcapsule formulations for extending the residual property of medicine of Bassa
KR102428031B1 (en) * 2021-12-07 2022-08-02 내외코리아 주식회사 Method for producing antibacterial virus coating composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107047557A (en) * 2016-12-14 2017-08-18 安徽东健化工科技有限公司 A kind of microcapsule formulations for extending the residual property of medicine of Bassa
KR102428031B1 (en) * 2021-12-07 2022-08-02 내외코리아 주식회사 Method for producing antibacterial virus coating composition

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