JPH03223205A - Boric acid solution and insecticide - Google Patents

Boric acid solution and insecticide

Info

Publication number
JPH03223205A
JPH03223205A JP29891390A JP29891390A JPH03223205A JP H03223205 A JPH03223205 A JP H03223205A JP 29891390 A JP29891390 A JP 29891390A JP 29891390 A JP29891390 A JP 29891390A JP H03223205 A JPH03223205 A JP H03223205A
Authority
JP
Japan
Prior art keywords
boric acid
solution
insecticide
polyhydric alcohol
weight
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
JP29891390A
Other languages
Japanese (ja)
Inventor
Yasunobu Mineki
峯木 安信
Minoru Mori
森 実
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.)
AGC Inc
Original Assignee
Asahi Glass 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 Asahi Glass Co Ltd filed Critical Asahi Glass Co Ltd
Publication of JPH03223205A publication Critical patent/JPH03223205A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide a safe and easily applicable insecticide, especially an insecticide for protecting wood from termite, comprising a homogeneous boric acid solution containing an ammonia derivative and a polyhydric alcohol and containing boric acid in high concentration. CONSTITUTION:A boric acid solution having high concentration is produced by adding an ammonia derivative and a polyhydric alcohol to boric acid, thereby increasing the solubility of boric acid. The boric acid solution having high concentration is used as an insecticide, especially insecticide for termite. Preferably, 0.2-5 pts.wt. of ammonia derivative and 0.2-5 pts.wt. of polyhydric alcohol are used based on 1 pt.wt. of boric acid. It is especially preferable to use 0.2-5 pts.wt. of a polyhydric alcohol having amino group in the molecule based on 1 pt.wt. of boric acid. Since the solution is stable, it can be stored in the form of a solution having high concentration and used after proper dilution. It exhibits mildewcidal effect as well as insecticidal effect.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、ホウ酸溶液およびそのホウ酸溶液からなる殺
虫剤、特に白アリから木材を守るための殺虫剤に間する
ものである。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a boric acid solution and an insecticide comprising the boric acid solution, particularly an insecticide for protecting wood from termites.

(従来の技術) ホウ酸は、適度な殺虫作用を有する化合物であるため、
木材などに溶液の形でスプレーあるしAはハケ塗りで塗
布して、白アリ等の害を防ぐ目的で使用されている。
(Prior art) Boric acid is a compound that has a moderate insecticidal effect, so
It is used to prevent termites and other harmful insects by spraying it on wood, etc. in the form of a solution, or applying it with a brush.

しかしながら、ホウ酸は表1に示すように一般の溶媒に
は溶けに(く、高濃度で均一な溶液力S得られないため
、木材に塗布しても十分な効果力≦得られない場合があ
った。(表1において、グI)セリンは比較的高い溶解
度を示しているが、ホウ酸のグリセリン溶液は、グリセ
リンに吸湿性があるため、木材などに塗布しても長期間
ベトつし1で実用上不都合が多い。) 表 1 (発明が解決しようとする課題) 本発明の目的は、ホウ酸を高濃度で含む均質な溶液を得
て、安全で使用しやすい殺虫剤を提供することである。
However, as shown in Table 1, boric acid is difficult to dissolve in common solvents and cannot provide a uniform solution strength at high concentrations, so even if applied to wood, sufficient effectiveness may not be obtained. (G I in Table 1) Serine has a relatively high solubility, but a boric acid glycerin solution does not remain sticky for a long time even when applied to wood etc. because glycerin is hygroscopic. Table 1 (Problems to be solved by the invention) The purpose of the present invention is to obtain a homogeneous solution containing boric acid at a high concentration, and to provide an insecticide that is safe and easy to use. That's true.

(課題を解決するための手段) 本発明は、アンモニア誘導体および多価アルコールを含
むホウ酸?容液からなる殺虫剤を提供するものである。
(Means for Solving the Problems) The present invention provides boric acid containing an ammonia derivative and a polyhydric alcohol. The present invention provides an insecticide consisting of a liquid solution.

本発明においては、アンモニア誘導体および多価アルコ
ールを含むことによりホウ酸が溶解しやすくなり、従来
知られていない高い濃度のホウ酸溶液が得られる。
In the present invention, boric acid is easily dissolved by containing an ammonia derivative and a polyhydric alcohol, and a boric acid solution with a high concentration hitherto unknown can be obtained.

本発明のホウ酸溶液は、ホウ酸1重量部に対して、アン
モニア誘導体0.2〜5重量部および多価アルコール0
.2〜5重量部を含むことが好ましい。ホウ酸1重量部
に対して、アンモニア誘導体0.5〜1゜5重量部およ
び多価アルコール0.5〜1.5重量部を含む場合は、
さらに好ましい。
The boric acid solution of the present invention contains 0.2 to 5 parts by weight of an ammonia derivative and 0 parts by weight of polyhydric alcohol per 1 part by weight of boric acid.
.. It is preferable to include 2 to 5 parts by weight. When containing 0.5 to 1.5 parts by weight of an ammonia derivative and 0.5 to 1.5 parts by weight of polyhydric alcohol per 1 part by weight of boric acid,
More preferred.

アンモニア誘導体としては、アンモニアおよび、第1級
アミン、第2級アミン、第3級アミン、第4級アンモニ
ウム塩のいずれも使用することができる。アンモニアを
始め揮発性の高いものを用いると、臭気が激しく作業が
困難となるので、適度の揮発性を有するものが良い。ア
ンモニア誘導体のなかで好ましいのは、第3級アミンで
ある。具体的には、アルキル第3級アミンが好ましく、
特に好ましいのは、トリエチルアミンである。
As the ammonia derivative, any of ammonia, primary amines, secondary amines, tertiary amines, and quaternary ammonium salts can be used. If a highly volatile material such as ammonia is used, the odor will be strong and the work will be difficult, so it is better to use a material with appropriate volatility. Among the ammonia derivatives, tertiary amines are preferred. Specifically, alkyl tertiary amines are preferred;
Particularly preferred is triethylamine.

本発明において用いる多価アルコールは、特に限定され
ず種々のものを用いることができる。例えば、エチレン
グリコール、プロピレングリコール、テトラメチレング
リコール、ペンタメチレングリコール、ヘキサメチレン
グリコール、ジエチレングリコール、ポリエチレングリ
コールなどの2価アルコール、グリセリンなどの3価ア
ルコール、エリトリットなどの4価アルコール、果糖、
マンノース、ガラクトースなどの糖類を挙げることがで
きる。
The polyhydric alcohol used in the present invention is not particularly limited, and various types can be used. For example, dihydric alcohols such as ethylene glycol, propylene glycol, tetramethylene glycol, pentamethylene glycol, hexamethylene glycol, diethylene glycol, polyethylene glycol, trihydric alcohols such as glycerin, tetrahydric alcohols such as erythritol, fructose,
Examples include sugars such as mannose and galactose.

これらのなかで、特に好ましいのは、エチレングリコー
ル、ジエチレングリコールあるいはポリエチレングリコ
ールである。
Among these, particularly preferred are ethylene glycol, diethylene glycol and polyethylene glycol.

本発明においては、ホウ酸と多価アルコールとアンモニ
ア誘導体の3者が反応して錯体を形成するため安定な1
液ができるものと考えられる。この3者の錯体が形成さ
れるには、水が必要である。ホウ酸と多価アルコールと
が反応する際には、水が生成するので、必ずしも水を初
めがら加える必要はない。
In the present invention, since the three components of boric acid, polyhydric alcohol, and ammonia derivative react to form a complex, a stable one
It is thought that liquid is formed. Water is required for the formation of this three-way complex. Since water is produced when boric acid and polyhydric alcohol react, it is not necessarily necessary to add water from the beginning.

本発明において、アンモニア誘導体として、分子内にア
ミノ基を有する多価アルコールを用いる場合は、アンモ
ニア誘導体自体が多価アルコールであるので、ほかに別
の多価アルコールを加えなくても、高濃度でも安定なホ
ウ酸溶液が得られる。分子内にアミノ基を有する多価ア
ルコールとしては、トリス(ヒドロキシアルキル)アミ
ンが好ましく、特に好ましいのは、トリエタノールアミ
ンである。
In the present invention, when a polyhydric alcohol having an amino group in the molecule is used as the ammonia derivative, since the ammonia derivative itself is a polyhydric alcohol, it can be used at high concentrations without adding another polyhydric alcohol. A stable boric acid solution is obtained. As the polyhydric alcohol having an amino group in the molecule, tris(hydroxyalkyl)amine is preferred, and triethanolamine is particularly preferred.

分子内にアミノ基を有する多価アルコールは、ホウ酸1
重量部に対して、0.2〜5重量部用いるのが好ましい
。ホウ酸1重量部に対して、0.5〜1.5重量部であ
る場合は、さらに好ましい。
A polyhydric alcohol having an amino group in its molecule is boric acid 1
It is preferable to use 0.2 to 5 parts by weight based on the weight part. More preferably, the amount is 0.5 to 1.5 parts by weight per 1 part by weight of boric acid.

分子内にアミノ基を有する多価アルコールを用いた場合
も、さらに分子内にアミン基のない多価アルコール0.
2〜5重量部を加えると、より安定な、@液が得られる
ので好ましい。ホウ酸1重量部に対して、0.5〜1.
5重量部である場合は、さらに好ましい。
Even when a polyhydric alcohol having an amino group in the molecule is used, a polyhydric alcohol without an amine group in the molecule is used.
It is preferable to add 2 to 5 parts by weight because a more stable @ liquid can be obtained. 0.5 to 1 part by weight of boric acid.
More preferably, the amount is 5 parts by weight.

本発明の溶液は、例えば以下のような方法で好適に製造
することができるが、必ずしもこれに限定されるもので
はない。
The solution of the present invention can be suitably produced, for example, by the following method, but is not necessarily limited thereto.

まず、水と多価アルコールを混合しておき、これを50
〜200°Cに加熱し、攪拌しながら所定量のホウ酸を
徐々に加える。このとき、ホウ酸は完全に溶解していな
くても良い。そして、加熱、撹拌を続けながら、アンモ
ニア誘導体を加えると、前述の錯形成反応が起こり均質
な溶液が得られる。
First, mix water and polyhydric alcohol, and add 50
Heat to ~200°C and gradually add the specified amount of boric acid while stirring. At this time, boric acid does not need to be completely dissolved. Then, when an ammonia derivative is added while continuing heating and stirring, the above-described complex formation reaction occurs and a homogeneous solution is obtained.

分子内にアミノ基を有する多価アルコールを用いる場合
は、所定量のホウ酸と混合してゆっくり加熱することに
より均一な溶液が得られる。これらの溶液に、水やアル
コールを加えて適宜希釈すると任意の濃度のホウ酸溶液
が得られる。
When using a polyhydric alcohol having an amino group in its molecule, a homogeneous solution can be obtained by mixing it with a predetermined amount of boric acid and slowly heating the mixture. If these solutions are appropriately diluted by adding water or alcohol, a boric acid solution of any concentration can be obtained.

このようなホウ酸溶液は、殺虫剤として好適に使用でき
る。
Such a boric acid solution can be suitably used as an insecticide.

本発明の殺虫剤においては、木材に塗布するために、他
に塗料として好適な樹脂成分を含むものであってもよい
The insecticide of the present invention may also contain a resin component suitable as a paint in order to be applied to wood.

本発明の殺虫剤は、木材に塗布して使用し、木材がシロ
アリあるいはキクイムシなどからの食害を防止すること
ができる。また同様に木材にカビが発生を妨げる効果も
有する。
The insecticide of the present invention can be applied to wood to prevent it from being damaged by termites, bark beetles, and the like. It also has the effect of preventing the growth of mold on wood.

(実施例) 実施例1 ポリエチレングリコール(分子量:約600) Log
と水10gを混合し、 100℃に加熱しながら、ホウ
酸20gを加え撹拌した。ホウ酸の一部が溶は残ってい
る状態でトリエチルアミンを25g加え、更に100℃
で加熱を続けたところ、5分後に無色透明で均質な溶液
(ホウ酸1度30,7重量%)が得られたので加熱をや
め放冷した。
(Example) Example 1 Polyethylene glycol (molecular weight: approximately 600) Log
and 10 g of water were mixed, and while heating to 100°C, 20 g of boric acid was added and stirred. Add 25g of triethylamine while some of the boric acid remains, and then heat to 100°C.
When heating was continued for 5 minutes, a colorless, transparent and homogeneous solution (boric acid 1°C, 30.7% by weight) was obtained, so heating was stopped and the solution was allowed to cool.

この溶液は、長期間保存しても白濁あるいは沈殿物は認
められなかった。また、この溶液は、水、アルコールで
任意の濃度に希釈することができた。
No cloudiness or precipitate was observed in this solution even after long-term storage. Moreover, this solution could be diluted to any concentration with water or alcohol.

実施例2 エチレングリコール20g、水log、トリエチルアミ
ン20g、ホウ酸20gを用いて実施例1と同様にして
無色透明なホウ酸溶液(ホウ酸濃度28.5重量%)を
得た。
Example 2 A colorless and transparent boric acid solution (boric acid concentration: 28.5% by weight) was obtained in the same manner as in Example 1 using 20 g of ethylene glycol, log water, 20 g of triethylamine, and 20 g of boric acid.

実施例3 エチレングリコール20g、水10g、トリエチルアミ
ン20g、ホウ酸30gを用いて、実施例1と同様にし
て無色透明なホウ酸溶液(ホウ酸濃度37.5重量%)
を得た。
Example 3 A colorless and transparent boric acid solution (boric acid concentration 37.5% by weight) was prepared in the same manner as in Example 1 using 20 g of ethylene glycol, 10 g of water, 20 g of triethylamine, and 30 g of boric acid.
I got it.

実施例4 ポリエチレングリコール(分子量:約600) Log
と水10gを混合し、 100℃に加熱しながら、ホウ
酸20gを加え撹拌した。ホウ酸の一部が溶は残ってい
る状態でトリエタノールアミンを25g加え、更に 1
00℃で加熱を続けたところ、5分後に無色透明で均質
な溶液が得られたので加熱をやめ放冷した。
Example 4 Polyethylene glycol (molecular weight: about 600) Log
and 10 g of water were mixed, and while heating to 100°C, 20 g of boric acid was added and stirred. Add 25g of triethanolamine while some of the boric acid remains, and add 1
Heating was continued at 00°C, and a colorless, transparent, homogeneous solution was obtained after 5 minutes, so heating was stopped and allowed to cool.

この溶液のホウ酸濃度は30.7重量%であった。The boric acid concentration of this solution was 30.7% by weight.

実施例5 エチレングリコール20g、水10g、トリエタノール
アミン20g、ホウ酸20gを用いて実施例1と同様に
して無色透明なホウ酸、@液(ホウ酸濃度28.5重量
%)を得た。
Example 5 A colorless and transparent boric acid solution (boric acid concentration: 28.5% by weight) was obtained in the same manner as in Example 1 using 20 g of ethylene glycol, 10 g of water, 20 g of triethanolamine, and 20 g of boric acid.

実施例6 エチレングリコール20g、水10g、トリエタノール
アミン20g、ホウ酸30gを用いて、実施例1と同様
にして無色透明なホウ酸溶液(ホウ酸濃度37.5重量
%)を得た。
Example 6 A colorless and transparent boric acid solution (boric acid concentration: 37.5% by weight) was obtained in the same manner as in Example 1 using 20 g of ethylene glycol, 10 g of water, 20 g of triethanolamine, and 30 g of boric acid.

実施例7 果糖15g、水10g、トリエタノールアミン20g、
ホウ酸25gを用いて実施例1と同様にして無色透明な
ホウ酸溶液(ホウ酸濃度35.7重量%)を得た。
Example 7 Fructose 15g, water 10g, triethanolamine 20g,
A colorless and transparent boric acid solution (boric acid concentration 35.7% by weight) was obtained in the same manner as in Example 1 using 25 g of boric acid.

実施例8 ガラクトース15g 、水log、トリエタノールアミ
ン20g、ホウ酸25gを用いて実施例1と同様にして
、無色透明なホウ酸溶液(ホウ酸濃度35.7重量%)
を得た。
Example 8 A colorless and transparent boric acid solution (boric acid concentration 35.7% by weight) was prepared in the same manner as in Example 1 using 15 g of galactose, log water, 20 g of triethanolamine, and 25 g of boric acid.
I got it.

実施例2〜8で得られた溶液は、実施例1の溶液と同様
、いずれも安定で、長期間保存しても白濁あるいは沈殿
物は認められなかった。また、この溶液は、水、アルコ
ールで任意の濃度に希釈することができた。
Like the solution of Example 1, the solutions obtained in Examples 2 to 8 were all stable, and no cloudiness or precipitate was observed even after long-term storage. Moreover, this solution could be diluted to any concentration with water or alcohol.

実施例9 ホウ酸40gにトリエタノールアミン40gを加え約1
20°Cに加熱し、10分間撹拌を行なって、透明なホ
ウ酸溶液を得た。この溶液を徐々に冷却して、100℃
になったときに室温の水を20g加えた。このようにし
て得られた40重量%のホウ酸溶液は長期間安定で、ま
た、水、アルコールで任意の濃度に希釈することができ
た。希釈液は室温で長期間放置しても、沈殿等を生じる
ことはなかった。
Example 9 Add 40 g of triethanolamine to 40 g of boric acid to give approx.
Heating to 20°C and stirring for 10 minutes gave a clear boric acid solution. This solution was gradually cooled to 100°C.
When the temperature reached 20 g, room temperature water was added. The 40% by weight boric acid solution thus obtained was stable for a long period of time and could be diluted with water or alcohol to any desired concentration. Even when the diluted solution was left at room temperature for a long period of time, no precipitation occurred.

実施例10 ホウ酸70gにトリエタノールアミン30gを加え約1
20℃に加熱し、20分間撹拌を行なって、透明で粘稠
なホウ酸溶液を得た。この溶液を徐々に冷却して、10
0℃になったときに室温のエタノールを250g加えた
。このホウ酸溶液は長期間安定で、室温で長期間放置し
ても沈殿等を生じることはない。
Example 10 Add 30 g of triethanolamine to 70 g of boric acid to give approx.
The mixture was heated to 20° C. and stirred for 20 minutes to obtain a clear and viscous boric acid solution. The solution was gradually cooled and
When the temperature reached 0° C., 250 g of room temperature ethanol was added. This boric acid solution is stable for a long period of time and does not cause precipitation even if left at room temperature for a long period of time.

エタノールに代えて、メタノールあるいはエタノールと
メタノールの混合溶7夜を用いても同様に安定なな溶液
が得られた。これらの/8液は、いずれも水、アルコー
ルで任意の濃度に希釈することができた。この希釈液は
室温で長期間放置しても沈殿等を生じることはなかった
A similarly stable solution was obtained by using methanol or a mixed solution of ethanol and methanol for 7 days instead of ethanol. All of these /8 solutions could be diluted with water or alcohol to any desired concentration. This diluted solution did not cause precipitation even when left at room temperature for a long period of time.

実施例11 ホウ酸100gにトリエタノールアミン40gを加え約
120℃に加熱し、20分間攪拌を行なって、透明で粘
稠なホウ酸溶液を得た。この溶液を徐々に冷却して、1
00℃になったときに室温のメタノールとエタノールの
1=1a合溶液355gを加えた。
Example 11 40 g of triethanolamine was added to 100 g of boric acid, heated to about 120° C., and stirred for 20 minutes to obtain a transparent and viscous boric acid solution. This solution was gradually cooled and
When the temperature reached 00°C, 355 g of a 1=1a combined solution of methanol and ethanol at room temperature was added.

この溶液にメラミン−ホルムアルデヒド樹脂(三井東圧
化学社製;サイメル325■)25gと重合開始剤(三
井東圧化学社製: Catalyst−6000)0、
25g加えた。透明な溶液が得られ、この、@液も長期
間保存しても安定であった。
To this solution were added 25 g of melamine-formaldehyde resin (manufactured by Mitsui Toatsu Chemical Co., Ltd.; Cymel 325■) and 0 of a polymerization initiator (manufactured by Mitsui Toatsu Chemical Co., Ltd.: Catalyst-6000).
Added 25g. A clear solution was obtained, and this @ solution was also stable even after long-term storage.

実施例12 ホウ酸100gにトリエタノールアミン40gを加え約
120°Cに加熱し、20分間撹拌を行なって、透明で
粘稠なホウ酸溶液を得た。この溶液を徐々に冷却して、
100℃になったときに室温のメタノールとエタノール
の1・1混合溶を夜355gを加えた。
Example 12 40 g of triethanolamine was added to 100 g of boric acid, heated to about 120°C, and stirred for 20 minutes to obtain a transparent and viscous boric acid solution. This solution is gradually cooled and
When the temperature reached 100° C., 355 g of a 1:1 mixed solution of methanol and ethanol at room temperature was added overnight.

この溶液にポリエチレングリコールメタクリレート25
gを加えて、均一な溶液を得た。この溶液も長期間保存
しても安定であった。
Add 25% polyethylene glycol methacrylate to this solution.
g was added to obtain a homogeneous solution. This solution was also stable even after long-term storage.

実施例13 アカマツ(学名pimus densiflora )
材の表面に実施例11の溶液を塗布量200g/m2で
塗布し、60℃で10時間乾燥した。イエシロアリ(学
名Coptotermies formosamus 
)が営巣しているアカマツ切株の周辺に処理したアカマ
ツ材と、比較のための無処理のアカマツ材を、それぞれ
5本交互に均等間隔で埋設した。
Example 13 Red pine (scientific name pimus densiflora)
The solution of Example 11 was applied to the surface of the material at a coating amount of 200 g/m 2 and dried at 60° C. for 10 hours. Coptotermies formosamus (scientific name: Coptotermies formosamus)
) were buried around the red pine stumps where they were nesting. Five treated red pine trees and five untreated red pine trees for comparison were alternately buried at equal intervals.

1年後、これらの試験片を引き抜いて、観察したところ
。処理を行なった試験片は、1本のみが一部にイエシロ
アリの食害を受けていたが、他の4本は全(食害を受け
ていなかった。無処理試験片は、すべてイエシロアリの
食害を受けていた。
One year later, these specimens were pulled out and observed. Of the treated test specimens, only one had been partially damaged by termites, but the other four had not suffered any damage.All of the untreated specimens had suffered damage from termites. was.

実施例14 実施例1.5.12の/g ’t&について、それぞれ
実施例13と同様なイエシロアリの食害試験を行なった
。いずれも、実施例11の溶液と同様に、はとんど食害
を受けていなかった。
Example 14 For /g't& of Examples 1, 5, and 12, the same termite damage test as in Example 13 was conducted. In both cases, similar to the solution of Example 11, there was almost no feeding damage.

実施例15 ホウ酸70gにトリエタノールアミン30gを加え約1
20℃に加熱し、20分間攪拌を行なって、透明で粘稠
なホウ酸溶液を得た。この溶液を徐々に冷却して、10
0℃になったときに室温のエタノールを250g加え、
ホウ酸溶液を得た。
Example 15 Add 30 g of triethanolamine to 70 g of boric acid to give approx.
The mixture was heated to 20° C. and stirred for 20 minutes to obtain a transparent and viscous boric acid solution. The solution was gradually cooled and
When the temperature reached 0℃, add 250g of room temperature ethanol,
A boric acid solution was obtained.

この溶液をエタノールで更に2倍に希釈して、ホウ酸濃
度10重量%の溶液を得た。ラワン材試験片(10mm
X 50n+m8100mm )の50mmX 100
mmの面の片方にこの溶液を130g/m”の塗布量で
塗布し、室温で14日間、40℃の恒温器中で30日間
放置したものを使用した。
This solution was further diluted twice with ethanol to obtain a solution with a boric acid concentration of 10% by weight. Lauan material test piece (10mm
x 50n+m8100mm) 50mm x 100
This solution was applied at a coating amount of 130 g/m'' to one side of the 2 mm surface, and the sample was left at room temperature for 14 days and in a thermostat at 40° C. for 30 days.

10mmX 50mmX 100mmのアルミ板に直径
2mmの穴を32個あけ、この中に、キクイムシ(学名
Lyctusbrunneus 5teph、)の幼虫
(体重2〜3mg)をそれぞれ1匹ずつ入れ、両側を上
記ラワン材を塗布面がアルミニウムに接するように挟ん
でゴムバンドで同定した。それぞれの穴には、小麦粉、
酵母粉末、セルロース粉末の混合物充填した。この試験
片を25°C1関係湿度70〜75%に保った。ホウ酸
溶液で処理した試験片と処理をしない試験片について、
3か月観測した。食害孔の数を測定し、羽化して成虫が
脱出した数を測定した。ホウ酸溶液で処理したものは、
食害孔数10、羽化脱出数が0であった。処理しないも
のは、食害孔数29、羽化脱出数が20であった。
Drill 32 holes with a diameter of 2 mm in a 10 mm x 50 mm x 100 mm aluminum plate, place one bark beetle (scientific name: Lyctus brunneus 5teph) larva (weight 2-3 mg) in each hole, and apply the lauan material on both sides. It was identified with a rubber band by holding it so that it was in contact with the aluminum. Fill each hole with flour,
Filled with a mixture of yeast powder and cellulose powder. This test piece was maintained at 25°C1 relative humidity of 70-75%. For specimens treated with boric acid solution and specimens without treatment,
Observed for 3 months. The number of feeding holes was measured, and the number of adults that emerged and escaped. Those treated with boric acid solution are
The number of feeding holes was 10, and the number of escapees was 0. Those that were not treated had 29 feeding damage holes and 20 emergence escapes.

実施例16 実施例4.5.11の/8/?!について、それぞれ実
施例15と同様なイエシロアリの食害試験を行なった。
Example 16 Example 4.5.11 /8/? ! For each of these, the same feeding damage test for Japanese termites as in Example 15 was conducted.

結果を表2に示す。The results are shown in Table 2.

表 (発明の効果) 本発明のホウ酸溶液は、ホウ酸を高濃度で含むことがで
きる。この溶液は安定で、かつ任意の濃度に希釈するこ
とができるので高濃度の溶液で貯蔵しておき、適宜希釈
して用いることもできる。
Table (Effects of the Invention) The boric acid solution of the present invention can contain boric acid at a high concentration. This solution is stable and can be diluted to any concentration, so it can be stored as a highly concentrated solution and used after being diluted as appropriate.

本発明の溶液を殺虫剤として使用する場合は、安全で、
適度な殺虫効果を有する。この溶液を木材等に塗布する
ことにより、高い防虫効果を得ることができ、特に白ア
リおよびキクイムシの被害から木材を守るために好適で
ある。
When using the solution of the invention as an insecticide, it is safe and
Has moderate insecticidal effect. By applying this solution to wood, etc., a high insect repellent effect can be obtained, and it is particularly suitable for protecting wood from damage by termites and bark beetles.

Claims (4)

【特許請求の範囲】[Claims] (1)アンモニア誘導体および多価アルコールを含むホ
ウ酸溶液からなる殺虫剤。
(1) An insecticide consisting of a boric acid solution containing an ammonia derivative and a polyhydric alcohol.
(2)ホウ酸1重量部に対して、アンモニア誘導体0.
2〜5重量部および多価アルコール0.2〜5重量部を
含むことを特徴とするホウ酸溶液。
(2) 0.0% ammonia derivative per 1 part by weight of boric acid.
A boric acid solution containing 2 to 5 parts by weight and 0.2 to 5 parts by weight of a polyhydric alcohol.
(3)ホウ酸1重量部に対して、分子内にアミノ基を有
する多価アルコール0.2〜5重量部を含むことを特徴
とするホウ酸溶液。
(3) A boric acid solution containing 0.2 to 5 parts by weight of a polyhydric alcohol having an amino group in the molecule per 1 part by weight of boric acid.
(4)請求項1または請求項2のホウ酸溶液からなる殺
虫剤。
(4) An insecticide comprising the boric acid solution according to claim 1 or claim 2.
JP29891390A 1989-11-07 1990-11-06 Boric acid solution and insecticide Pending JPH03223205A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP1-287818 1989-11-07
JP28781889 1989-11-07

Publications (1)

Publication Number Publication Date
JPH03223205A true JPH03223205A (en) 1991-10-02

Family

ID=17722160

Family Applications (1)

Application Number Title Priority Date Filing Date
JP29891390A Pending JPH03223205A (en) 1989-11-07 1990-11-06 Boric acid solution and insecticide

Country Status (1)

Country Link
JP (1) JPH03223205A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1025967A1 (en) * 1999-01-25 2000-08-09 Lonza AG Wood treatment agent
KR20040072778A (en) * 2003-02-11 2004-08-19 김성옥 Insecticide

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1025967A1 (en) * 1999-01-25 2000-08-09 Lonza AG Wood treatment agent
KR20040072778A (en) * 2003-02-11 2004-08-19 김성옥 Insecticide

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