JPS593441B2 - Slowly soluble insecticide - Google Patents
Slowly soluble insecticideInfo
- Publication number
- JPS593441B2 JPS593441B2 JP49014772A JP1477274A JPS593441B2 JP S593441 B2 JPS593441 B2 JP S593441B2 JP 49014772 A JP49014772 A JP 49014772A JP 1477274 A JP1477274 A JP 1477274A JP S593441 B2 JPS593441 B2 JP S593441B2
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- insecticide
- polymer
- slowly soluble
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- 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.)
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Description
【発明の詳細な説明】
本発明は新規にして有用な徐溶性殺虫剤に関するもので
ある。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a new and useful slowly soluble insecticide.
近年においては、樹脂工業の飛躍的発展に伴い、その莫
大な生産量が消費されると共に、莫大な量の廃棄物が生
成し、公害の原因となっている。In recent years, with the rapid development of the resin industry, a huge amount of its production has been consumed, and a huge amount of waste has been generated, causing pollution.
かかる公害の原因を解消する為に、これらプラスチック
材料を廃棄物公害の発生しない材料に改質せんとする研
究、たとえば、樹脂材料に要求される本来の要件である
熱や光等に対する安定性とは反対に、熱や光等によって
容易に分解し得る樹脂材料の開発が課題となっているが
、未だ満足し得る技術は提供されていない。In order to eliminate the causes of such pollution, research is being conducted to modify these plastic materials into materials that do not generate waste pollution, such as improving stability against heat and light, which is the original requirement for resin materials. On the contrary, the challenge is to develop resin materials that can be easily decomposed by heat, light, etc., but no satisfactory technology has been provided yet.
一方、これらプラスチック廃棄物を■焼却、■再生、■
微生物分解、等によって処理する方法が知られているが
、■の方法は有毒ガスの発生によって2次公害を生ずる
他、燃焼熱量が太きいために焼却炉の耐用年数が短かい
等の問題があり、■においては、これら廃棄物を土地造
成や道路舗装に用いる試みが行なわれている。On the other hand, these plastic wastes can be ■ incinerated, ■ recycled, and ■
Methods such as microbial decomposition are known, but method (2) not only causes secondary pollution due to the generation of toxic gases, but also has problems such as a short service life of the incinerator due to the large amount of combustion heat. Yes, and in ■, attempts are being made to use these wastes for land development and road paving.
■においては、微生物の作用によってこれら廃棄物を分
解する方法が研究され、かつ発表されている。In (2), a method for decomposing these wastes through the action of microorganisms has been researched and announced.
しかしながら、斜上の如き方法は、処理方法の繁雑さ、
処理費用あるいは2次公害防止等の観点から満足し得る
ものでない。However, the diagonal method is complicated,
This is not satisfactory from the viewpoint of treatment costs or prevention of secondary pollution.
しかるに、実用性を備え、かつ廃棄物公害を生ずること
のない樹脂組成物が提供され〜ば、廃棄物処理の点から
極めて有用となるのであるが、その様な樹脂組成物は殆
んど知られていない。However, if a resin composition that is practical and does not cause waste pollution could be provided, it would be extremely useful in terms of waste treatment, but such resin compositions are hardly known. It has not been done.
本発明者等は、かかる事情に着眼し種々研究を重ねた結
果無機酸化物とアルカリ金属塩との焼成物■及び不飽和
カルボン酸の重合体もしくは共重合体■を配合してなる
徐溶性組成物を開発するに至った。The present inventors focused on this situation and conducted various studies, and as a result, the present inventors discovered a slowly soluble composition comprising a fired product (1) of an inorganic oxide and an alkali metal salt and a polymer or copolymer (2) of an unsaturated carboxylic acid. I ended up developing something.
即ちこの組成物は実用にかなう保形性及び成形性を有す
ると共に、水に徐々に溶解するという特異な特性を有し
ており、雨水等によって徐々に溶解し消滅するので廃棄
物公害を生じることがない。In other words, this composition has practical shape retention and moldability, and also has the unique property of gradually dissolving in water, and as it gradually dissolves and disappears in rainwater, etc., it does not cause waste pollution. There is no.
本発明者等はこの様な徐溶性組成物の特徴を各種殺虫剤
との組合わせにおいて有効に活用すべく更に研究の結果
完成されたものであって、その構成は、前記■及び■と
共に殺虫剤■を配合し、殺虫剤■を徐々に放出させる様
にしたところに要旨が存在する。The present inventors have completed further research to effectively utilize the characteristics of such slowly soluble compositions in combination with various insecticides. The gist lies in the fact that the insecticide (2) is blended and the insecticide (2) is gradually released.
本発明に係る徐溶性殺虫剤を構成する焼成物■は、無機
酸化物とアルカリ金属塩とを焼成することによって得ら
れる。The baked product (1) constituting the slowly soluble insecticide according to the present invention is obtained by baking an inorganic oxide and an alkali metal salt.
無機酸化物としては、周期律表第1族から第■族に及ぶ
多種類の元素の酸化物を使用することができ、たとえば
、銅等の銅族元素、ベリリウム、マグネシウム、カルシ
ウム、ストロンチウム、バリウム等のアルカリ土類金属
元素、能鉛等の亜鉛族元素、硼素、アルミニウム等のア
ルミニウム族元素、珪素、錫、鉛等の炭素元素、チタン
、ジルコニウム等のチタン族元素、アンチモン等の窒素
族元素、バナジウム等のバナジウム族元素、クロム、モ
リブデン等のクロム族元素、マンガン等のマンガン族元
素、鉄、コバルト、ニッケル等の鉄族元素、等の金属も
しくは非金属の酸化物が挙げられる。As the inorganic oxide, oxides of various elements ranging from Group 1 to Group II of the periodic table can be used, such as copper group elements such as copper, beryllium, magnesium, calcium, strontium, and barium. alkaline earth metal elements such as lead, zinc group elements such as lead, aluminum group elements such as boron and aluminum, carbon elements such as silicon, tin, and lead, titanium group elements such as titanium and zirconium, nitrogen group elements such as antimony. , vanadium group elements such as vanadium, chromium group elements such as chromium and molybdenum, manganese group elements such as manganese, iron group elements such as iron, cobalt, and nickel, and metal or nonmetal oxides.
またアルカリ金属塩とは、リチウム、ナトリウム、カリ
ウム等のハロゲン化物、水酸化物、炭酸塩、重炭酸塩、
硝酸塩等の無機塩、蟻酸塩、酢酸塩等の有機塩が例示さ
れ、これらは1種もしくは2種以上の混合物として使用
してもよい。Alkali metal salts include halides, hydroxides, carbonates, bicarbonates, etc. of lithium, sodium, potassium, etc.
Examples include inorganic salts such as nitrates, and organic salts such as formates and acetates, and these may be used alone or as a mixture of two or more.
該アルカリ金属塩は徐溶性と密接に関連しており、これ
を増減することによって徐溶性の程度を広範囲に選択調
整し得る。The alkali metal salt is closely related to slow solubility, and by increasing or decreasing its content, the degree of slow solubility can be selectively adjusted over a wide range.
しかして、該アルカリ金属の使用割合は、該組成物の徐
溶性の程度に応じて広範囲に変化し得るので特に限定を
設けるべきでないが、通常は、溶解性の高い組成物な得
ようとする場合は、不飽和カルボン酸重合体100重量
部に対し50〜200重量部、溶解性の低い組成物を得
んとする場合は、1〜50重量部、の範囲から任意に選
択される。Therefore, the proportion of the alkali metal to be used can vary over a wide range depending on the degree of slow solubility of the composition and should not be particularly limited; however, it is usually desired to obtain a composition with high solubility. In this case, the amount is arbitrarily selected from the range of 50 to 200 parts by weight per 100 parts by weight of the unsaturated carboxylic acid polymer, and in the case of obtaining a composition with low solubility, the amount is arbitrarily selected from the range of 1 to 50 parts by weight.
ところで、酸化物とアルカリ金属塩とを焼成する際の条
件は、500℃以上の高温であればよ(、殊に好ましい
のは、900〜1300℃の範囲であり、その温度範囲
内では、2〜10時間程度焼成するのがよい。Incidentally, the conditions for firing the oxide and the alkali metal salt may be as high as 500°C or higher (particularly preferably in the range of 900 to 1300°C; within that temperature range, It is best to bake for about 10 hours.
尚、前記焼成においては焼成温度を低くし、あるいは焼
成時間を短か(するに従って、(これを不飽和カルボン
酸重合体と混合して得られる)徐溶性組成物の溶解性は
高くなる傾向があるので、焼成温度及び焼成時間は、目
的とする徐溶性の程度に応じて適宜に選択して決定され
る。In addition, in the above-mentioned calcination, the solubility of the slowly soluble composition (obtained by mixing it with an unsaturated carboxylic acid polymer) tends to increase as the calcination temperature is lowered or the calcination time is shortened. Therefore, the firing temperature and firing time are appropriately selected and determined depending on the desired degree of slow solubility.
又、焼成物■は、不飽和カルボン酸重合物との練和を容
易かつ完全に行なう為に、通常300メツシユ以下の微
粒子に粉砕して使用される。In addition, the fired product (2) is usually used after being ground into fine particles of 300 mesh or less in order to easily and completely knead it with the unsaturated carboxylic acid polymer.
不飽和カルボン酸の重合物もしくは共重合物■は、アク
リル酸、メタクリル酸、フマル酸、マレイン酸、クロト
ン酸、ビニル酢酸、桂皮酸等の不飽和カルボン酸を、従
来公知の方法で単独重合もしくは共重合して得られる粘
稠液である。Polymers or copolymers of unsaturated carboxylic acids (2) are obtained by homopolymerizing or copolymerizing unsaturated carboxylic acids such as acrylic acid, methacrylic acid, fumaric acid, maleic acid, crotonic acid, vinyl acetic acid, and cinnamic acid by conventionally known methods. It is a viscous liquid obtained by copolymerization.
重合方法は特に限定されないが、通常採用される方法を
例示すれば下記の如(である。The polymerization method is not particularly limited, but examples of commonly employed methods are as follows.
■ 不飽和カルボン酸の単独物または混合物にベンゾフ
ェノン、アセトンなどの光増感剤を添加し、水溶液中で
高圧水銀灯等によって紫外線を照射して重合させる。(2) A photosensitizer such as benzophenone or acetone is added to unsaturated carboxylic acids alone or as a mixture, and the mixture is polymerized by irradiation with ultraviolet rays using a high-pressure mercury lamp or the like in an aqueous solution.
■ 不飽和カルボン酸の単独物または混合物に、0.5
〜5.0重量%の遊離基触媒、例えば過硫酸アンモニウ
ム、過硫酸カリウム、過硫酸ナトリウム等、を添加し、
窒素雰囲気下、80〜100℃の温度で水溶液重合する
。■ Unsaturated carboxylic acids alone or in mixture, 0.5
adding ~5.0% by weight of a free radical catalyst, such as ammonium persulfate, potassium persulfate, sodium persulfate, etc.;
Aqueous solution polymerization is carried out at a temperature of 80 to 100°C under a nitrogen atmosphere.
この際、必要に応じて適宜量の重合度調整剤、例えばイ
ソプロピルアルコール、を添加する場合もある。At this time, an appropriate amount of a degree of polymerization regulator, such as isopropyl alcohol, may be added as necessary.
かくして得られる焼成物■と重合物■とを、たとえば前
者1部に対して後者011〜5部の割合で練和し、次い
で静置すると、4〜30分間で固化し硬い樹脂が得られ
る。The thus obtained baked product (1) and polymer (2) are kneaded in a ratio of, for example, 1 part of the former to 0.11 to 5 parts of the latter, and then left to stand, solidifying in 4 to 30 minutes to obtain a hard resin.
従ってこれらを所定割合で練和した後、所望の型枠に圧
入して固定させれば、任意形状の成形物が得られる。Therefore, by kneading these in a predetermined ratio and press-fitting and fixing them into a desired mold, a molded product of any shape can be obtained.
しかして該成形物は、水と接触するとその表面から徐々
に溶解し、いわゆる徐溶性を有するのであるが、徐溶性
の程度は、焼成物■に使用されるアルカリ金属塩の量を
増減することによって任意に調節することが出来る。However, when the molded product comes into contact with water, it gradually dissolves from its surface and has so-called slow solubility, but the degree of slow solubility can be determined by increasing or decreasing the amount of the alkali metal salt used in the baked product. It can be adjusted arbitrarily by
本発明の徐溶性殺虫剤は、前記徐溶性組成物に農業用ま
たは公衆衛生用殺虫剤■を含有せしめることによって得
られる。The slowly soluble insecticide of the present invention can be obtained by incorporating agricultural or public health insecticide (2) into the slowly soluble composition.
即ち、前記徐溶性組成物に殺虫剤■を含有せしめれば、
徐溶性組成物が水に徐々に溶解するにつれて殺虫剤■を
も徐々に溶出するので、徐溶性組成物の徐溶性の程度を
任意に調節することによって、殺虫剤■の徐放性を自由
に調整し得るものである。That is, if the slowly soluble composition contains the insecticide (2),
As the slowly soluble composition gradually dissolves in water, the insecticide ■ gradually dissolves, so by arbitrarily adjusting the degree of slow solubility of the slowly soluble composition, the sustained release of the insecticide ■ can be freely controlled. It can be adjusted.
かかる殺虫剤■としては、極めて広汎のものを適用する
ことができ、代表的なものとしては各種農業用殺虫剤や
公衆衛生用の各種殺虫剤が挙げられるが、この他防腐剤
、防かび剤、殺菌剤等も本発明でいう殺虫剤の範囲に含
まれる。A very wide range of insecticides can be used as such insecticides, and typical examples include various agricultural insecticides and various insecticides for public health, but there are also preservatives and fungicides. , fungicides, etc. are also included within the scope of the insecticides referred to in the present invention.
これら殺虫剤■を徐溶性組成物に含有せしめる方法は特
に限定されるものではなく、たとえば焼成物■の粉末ま
たは不飽和カルボン酸重合体■の溶液に均一に分散もし
くは溶解させる方法、あるいは前記■■の練和時に殺虫
剤■を添加し、同時に練和する方法のいずれも採用する
ことができる。The method of incorporating these insecticides (1) into the slowly soluble composition is not particularly limited. Any of the methods of adding the insecticide (2) at the time of kneading (2) and kneading at the same time can be adopted.
本発明殺虫剤は以上の如(徐溶性という特異な性質を有
しているので、殺虫効果の持続性が極めて良好であると
共に、地中等に施用したときの分散ロスが少なく、しか
も一気に大量の殺虫剤が拡散する恐れがないので、薬害
が著しく緩和される等、幾多の利益を享受し得るもので
ある。As described above, the insecticide of the present invention has the unique property of slow solubility, so it has an extremely long-lasting insecticidal effect, has little dispersion loss when applied underground, and can be applied in large quantities at once. Since there is no fear of the insecticide spreading, it is possible to enjoy many benefits such as significantly reducing chemical damage.
次に、本発明を参考例及び実施例によって説明する。Next, the present invention will be explained by reference examples and examples.
参考例 1
〔焼成物製造例〕
焼成塩1)酸化叱鉛 50重量部酸化マグネ
シウム 40重量部
フッ化ナトリウム 10重量部
上記の配合物を1000℃で3時間焼成した後、ジェッ
ト粉砕し300メツシユ以下の粒子の粉末とする。Reference Example 1 [Example of producing baked products] Baking salt 1) Lead oxide 50 parts by weight Magnesium oxide 40 parts by weight Sodium fluoride 10 parts by weight The above mixture was fired at 1000°C for 3 hours and then jet-pulverized to 300 mesh or less. powder of particles.
焼成物(2)酸化叱鉛 50重量部酸化マグ
ネシウム 30重量部
フッ化カリウム 10重量部
上記の配合物を1000℃で2時間焼成した後、ジェッ
ト粉砕し300メツシユ以下の粒子の粉末とする。Calcined product (2) Lead oxide 50 parts by weight Magnesium oxide 30 parts Potassium fluoride 10 parts by weight The above mixture was fired at 1000° C. for 2 hours and then jet-pulverized to form a powder with particles of 300 mesh or less.
焼成1に3) 酸化能鉛 40重量部酸化
マグネシュウム 20重量部
酸化力ルシュウム 20重量部
フッ化カリウム 20重量部
焼成vA4) 酸化徂鉛 40重量部酸化
珪素 30重量部
酸化マグネシウム 20重量部
フッ化ナトリウム 20重量部
焼成塩5)酸化能鉛 20重量部酸化マグネ
シュウム 60重量部
フッ化カリウム 10重量部
焼成物(6)酸化マグネシュウム 80重量部炭酸ナト
リウム 40重量部
酸化唾鉛 10重量部
前記粉末(3X4X5X6)の配合混合物はいずれも1
200℃5時間焼成して300メツシユ以下にジェット
粉砕した。3) Lead oxidation capacity 40 parts by weight Magnesium oxide 20 parts by weight Rusium oxidation capacity 20 parts by weight Potassium fluoride 20 parts by weight Calcination vA4) Lead oxide 40 parts by weight Silicon oxide 30 parts by weight Magnesium oxide 20 parts by weight Sodium fluoride 20 parts by weight Calcined salt 5) Oxidizing capacity Lead 20 parts by weight Magnesium oxide 60 parts by weight Potassium fluoride 10 parts by weight Calcined product (6) Magnesium oxide 80 parts by weight Sodium carbonate 40 parts by weight Saliva oxide 10 parts by weight The above powder (3X4X5X6) The blended mixtures are all 1
It was fired at 200° C. for 5 hours and jet-pulverized to 300 meshes or less.
重合機1) マレイン酸 60重量部アクリ
ル酸 10重量部
ベンゾフェノン 5重量部
蒸留水 100重量部
重合物(2)アクリル酸 80重量部クロトン
酸 10重量部
アセトン 5重量部
蒸留水 100重量部
重合物(3)フマル酸 40重量部メタアク
リル・酸 10重量部
ビニル酢酸 10重量部
アセトン 5重量部
蒸留水 100重量部
上記(1)(2X3)の配合物に1にW高圧水銀灯の紫
外線を照射した後、未反応物、溶媒を留去し重合物、共
重合物の濃度が40%になるまで濃縮した。Polymerizer 1) Maleic acid 60 parts by weight Acrylic acid 10 parts by weight Benzophenone 5 parts by weight Distilled water 100 parts by weight Polymer (2) Acrylic acid 80 parts by weight Crotonic acid 10 parts by weight Acetone 5 parts by weight Distilled water 100 parts by weight Polymer ( 3) Fumaric acid 40 parts by weight Methacrylic acid 10 parts by weight Vinyl acetic acid 10 parts by weight Acetone 5 parts by weight Distilled water 100 parts by weight After irradiating the blend of (1) (2X3) above with ultraviolet rays from a W high pressure mercury lamp. , unreacted substances and the solvent were distilled off, and the mixture was concentrated until the concentration of the polymer and copolymer was 40%.
粘度はそれぞれ11000CPS、14000CPS、
1oooocpsであった。The viscosity is 11000CPS, 14000CPS, respectively.
It was 1ooooocps.
重合物(4)アクリル酸 50重合部4 /
yoo e”iv 7 iv 10重量部コール
過硫酸ナトリウム 1重量部
蒸留水 150重量部
上記配合物のうちイングロビルアルコール、過硫酸ナト
リウムを蒸留水に混合して反応器に入れ、85℃±3℃
の温度に保ちアクリル酸をかく拌しながら3時間に亘っ
て滴下させて重合した。Polymer (4) Acrylic acid 50 polymer parts 4 /
yoo e”iv 7 iv 10 parts by weight Sodium cole persulfate 1 part by weight Distilled water 150 parts Among the above formulations, Inglobil alcohol and sodium persulfate were mixed with distilled water, put into a reactor, and heated to 85°C ± 3°C.
Acrylic acid was added dropwise over a period of 3 hours while stirring to polymerize.
反応終了後、水を減圧下で除去し重合物の濃度を35%
にした。After the reaction is complete, water is removed under reduced pressure to reduce the concentration of the polymer to 35%.
I made it.
平均分子量 50000、粘度12000 CP S0
重合物シ)マレイン酸 20重量部桂皮酸
5重量部
メタアクリル酸 10重量部
過硫酸アンモニウム 2重量部
蒸留水 100重量部
上記配合物も(4)と同様にして共重合させた。Average molecular weight 50000, viscosity 12000 CP S0
Polymer c) Maleic acid 20 parts by weight cinnamic acid
5 parts by weight Methacrylic acid 10 parts by weight Ammonium persulfate 2 parts by weight Distilled water 100 parts by weight The above formulation was also copolymerized in the same manner as in (4).
濃度40%、平均分子量20000.粘度
10000CPS0
重合物6)アクリル酸 40重量部メタアクリ
ル酸 10重量部
過硫酸アンモニウム 1重量部
蒸留水 150重量部
上記配合物も(4)と同様にして共重合させた。Concentration 40%, average molecular weight 20,000. Viscosity: 10,000 CPS0 Polymer 6) Acrylic acid: 40 parts by weight Methacrylic acid: 10 parts by weight Ammonium persulfate: 1 part by weight Distilled water: 150 parts by weight The above blend was also copolymerized in the same manner as in (4).
濃度43%、平均分子量25000.粘度
11000CPS0
前述の各焼成物と重合物もしくは共重合物を2:1(重
量部)の割合で練和して直径6mm、高さ12朋の円柱
状成形物を得た。Concentration 43%, average molecular weight 25000. Viscosity 11,000 CPS0 Each of the above-mentioned fired products and the polymer or copolymer were kneaded in a ratio of 2:1 (parts by weight) to obtain a cylindrical molded product with a diameter of 6 mm and a height of 12 mm.
25分後、表面が滑沢で、かつ硬い樹脂の成形物を得た
。After 25 minutes, a hard resin molding with a smooth surface was obtained.
次の表は、それぞれの成形物の物性を測定したものであ
る。The following table shows the measured physical properties of each molded product.
抗圧縮力は、直径6mm、高さ12mmの円柱形の試験
片を使用し圧縮試験機によって測定した。The anti-compressive force was measured using a compression tester using a cylindrical test piece with a diameter of 6 mm and a height of 12 mm.
溶解速度は、上記め試験片を20℃の蒸留水に浸漬し、
1週間後の減量%(重量)で示されている。The dissolution rate was determined by immersing the above test piece in distilled water at 20°C.
It is shown as % weight loss after 1 week.
実施例 1
S−(エチルスルフィニルメチル)−ジイソプロピルホ
スホロチオロチオネートを有効成分とする有機リン酸系
殺虫剤(IPSP剤)1重量部を、前記焼成物(1)1
0重量部及び重合物3)4重量部と共に均一に練和した
後造粒し、粒状殺虫剤を得た。Example 1 1 part by weight of an organophosphate insecticide (IPSP agent) containing S-(ethylsulfinylmethyl)-diisopropyl phosphorothiorothionate as an active ingredient was added to the baked product (1) 1
After uniformly kneading the mixture with 0 parts by weight and 4 parts by weight of polymer 3), the mixture was granulated to obtain a granular insecticide.
該殺虫剤を、タマネギを定植する際、根ぎわに殺虫剤の
有効成分が10〜15′?/株となる様に施用した場合
、生育期から収穫に至るまでネダニ、タマネギバエ等の
発生は見られなかった。When planting onions, the active ingredient of the insecticide is added to the roots of onions by 10 to 15'? When applied in such a way as to produce a total of 100% of plants, no outbreaks of mites, onion flies, etc. were observed from the growing season to harvest.
一方、IPSP粒剤をそのまま使用する場合は、生育期
間中に2〜3回に分割して施用するのであるが、これを
定植時一度に151/株を施用した場合は生育末期に前
記の害虫が発生した。On the other hand, when using IPSP granules as is, they are applied in two or three times during the growing period, but if 151/plant is applied at once at the time of planting, the above-mentioned pests will occur at the end of the growing season. There has occurred.
即ち本発明によれば、殺虫剤を分割して施用する必要が
な(、一度の施用で長期間殺虫効果を持続する。That is, according to the present invention, it is not necessary to apply the insecticide in parts (the insecticidal effect can be maintained for a long period of time with one application).
又、本発明の徐溶性殺虫剤は、希釈効果をも有するので
、施用時の薬害をも著しく緩和し、かつ徐放性であるの
で殺虫剤の地中での分散によるロスが少ない。Furthermore, since the slowly soluble insecticide of the present invention also has a diluting effect, it significantly alleviates chemical damage during application, and since it is sustained release, there is little loss due to dispersion of the insecticide underground.
Claims (1)
カルボン酸の重合体もしくは共重合体■及び殺虫剤■か
らなることを特徴とする、徐溶性殺虫剤。1. A slow-soluble insecticide characterized by consisting of a baked product (1) of an inorganic oxide and an alkali metal salt, (2) a polymer or copolymer of an unsaturated carboxylic acid, and (2) an insecticide.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP49014772A JPS593441B2 (en) | 1974-02-04 | 1974-02-04 | Slowly soluble insecticide |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP49014772A JPS593441B2 (en) | 1974-02-04 | 1974-02-04 | Slowly soluble insecticide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS50109243A JPS50109243A (en) | 1975-08-28 |
| JPS593441B2 true JPS593441B2 (en) | 1984-01-24 |
Family
ID=11870333
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP49014772A Expired JPS593441B2 (en) | 1974-02-04 | 1974-02-04 | Slowly soluble insecticide |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS593441B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6174922U (en) * | 1984-10-19 | 1986-05-21 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04216869A (en) * | 1990-12-18 | 1992-08-06 | Ishizuka Glass Co Ltd | Degradable plastic composition |
| JPH04216870A (en) * | 1990-12-18 | 1992-08-06 | Ishizuka Glass Co Ltd | Degradable plastic composition |
-
1974
- 1974-02-04 JP JP49014772A patent/JPS593441B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6174922U (en) * | 1984-10-19 | 1986-05-21 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS50109243A (en) | 1975-08-28 |
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