JPH072608A - Agrichemical solid formulation - Google Patents

Agrichemical solid formulation

Info

Publication number
JPH072608A
JPH072608A JP14495493A JP14495493A JPH072608A JP H072608 A JPH072608 A JP H072608A JP 14495493 A JP14495493 A JP 14495493A JP 14495493 A JP14495493 A JP 14495493A JP H072608 A JPH072608 A JP H072608A
Authority
JP
Japan
Prior art keywords
acephate
weight
parts
boron oxide
preparation
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
JP14495493A
Other languages
Japanese (ja)
Inventor
Yasuyuki Katayama
泰之 片山
Toshiro Otsubo
敏朗 大坪
Shii Hefuanan Danieru
シー ヘファナン ダニエル
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 JP14495493A priority Critical patent/JPH072608A/en
Priority to TW83101529A priority patent/TW296971B/zh
Priority to FR9403328A priority patent/FR2706247B1/en
Priority to KR1019940006604A priority patent/KR950000027A/en
Priority to US08/220,882 priority patent/US6335026B1/en
Priority to ITRM940217A priority patent/IT1272208B/en
Priority to EP94302727A priority patent/EP0629346A3/en
Priority to BR9401546A priority patent/BR9401546A/en
Priority to ES09400807A priority patent/ES2094681B1/en
Priority to CN94104296A priority patent/CN1096628A/en
Publication of JPH072608A publication Critical patent/JPH072608A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To improve the storage stability of acephate in an acephate technical product or in an agrichemical solid formulation containing the acephate by adding boron oxide and/or metaboric acid. CONSTITUTION:A method for stabilizing acephate comprises adding boron oxide and/or metaboric acid to an acephate technical product or an agrichemical solid formulation containing the acephate, and the acephate improved in storage stability adding the boron oxide and/or the metaboric acid.

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、アセフェートを含有す
る安定化された農薬固形製剤に関するものである。
TECHNICAL FIELD The present invention relates to a stabilized agricultural chemical solid preparation containing acephate.

【従来の技術】アセフェート(O,S−ジメチル アセ
チルホスホルアミドチオエート)は、The Pesticide Ma
nual第8版(1987年 The British Crop Protection Cou
ncil発行)第1頁に記載の殺虫活性を有する化合物であ
り、各種害虫の防除に有効なことから、現在農業用殺虫
剤の有効成分として用いられている。
2. Description of the Related Art Acephate (O, S-dimethyl acetylphosphoramidothioate) is used in The Pesticide Ma
nual 8th edition (1987 The British Crop Protection Cou
(published by Ncil), which is a compound having an insecticidal activity described on page 1, and is currently used as an active ingredient of agricultural insecticides because it is effective in controlling various pests.

【発明が解決しようとする課題】しかしながら、アセフ
ェートは農薬製剤中での安定性があまり高くないため、
保存条件によっては製剤中のアセフェートの分解が激し
く、その結果アセフェートの殺虫効力を有効に活かせな
いことがあった。そこで、アセフェートを含有する安定
な農薬製剤の開発が望まれていた。
However, since acephate is not very stable in pesticide formulations,
Depending on storage conditions, the acephate in the preparation was decomposed severely, and as a result, the insecticidal efficacy of acephate could not be effectively utilized. Therefore, it has been desired to develop a stable pesticide formulation containing acephate.

【0002】[0002]

【課題を解決するための手段】本発明は、(a)アセフ
ェート、(b)酸化硼素および/またはメタ硼酸および
(c)製剤用固形担体を含有する安定化された農薬固形
製剤を提供するものであり、酸化硼素またはメタ硼酸の
添加により、アセフェート原体または農薬固形製剤中の
アセフェートが安定化されることによるものである。ア
セフェートを安定化するのに有効な酸化硼素および/ま
たはメタ硼酸の量は、一般にアセフェート1重量部に対
して0.01〜0.5 重量部であるが、勿論それ以上の添加量
であっても何ら問題はない。
The present invention provides a stabilized pesticide solid formulation containing (a) acephate, (b) boron oxide and / or metaboric acid, and (c) a solid carrier for formulation. This is because the addition of boron oxide or metaboric acid stabilizes the acephate drug substance or the acephate in the agricultural chemical solid preparation. The amount of boron oxide and / or metaboric acid effective for stabilizing acephate is generally 0.01 to 0.5 parts by weight per 1 part by weight of acephate, but of course no problem will occur even if it is added in excess. Absent.

【0003】本発明において、農薬固形製剤中のアセフ
ェートの含有量は一般に0.5〜99重量%、好ましく
は5〜95重量%であり、安定化剤である酸化硼素およ
び/またはメタ硼酸の含有量は、アセフェートを安定化
するのに必要な量、通常0.01〜50重量%、好まし
くは1〜20重量%、より好ましくは1〜10重量%で
ある。本発明において用いられる製剤用固形担体として
は、カオリンクレー、アタパルジャイトクレー、セリサ
イトクレー、パイロフィライトクレー、モンモリロナイ
トクレー、ゼオライト、ベントナイト、酸性白土、活性
白土、蛇紋岩、タルク、珪藻土などの鉱物質担体、硫酸
塩、硝酸塩、塩化物などの無機塩、シリカなどの合成担
体等の無機質担体、糖類、澱粉、デキストリン、小麦
粉、大豆粉、トウモロコシ粉、木粉等の有機質担体が挙
げられる。これらの製剤用固形担体は、本発明の農薬固
形製剤中に、通常1〜90重量%、好ましくは20〜7
0重量%含有される。
In the present invention, the content of acephate in the agricultural chemical solid preparation is generally 0.5 to 99% by weight, preferably 5 to 95% by weight, and the stabilizer boron oxide and / or metaboric acid is contained. The amount is necessary to stabilize the acephate, usually 0.01 to 50% by weight, preferably 1 to 20% by weight, more preferably 1 to 10% by weight. As the solid carrier for the formulation used in the present invention, kaolin clay, attapulgite clay, sericite clay, pyrophyllite clay, montmorillonite clay, zeolite, bentonite, acid clay, activated clay, serpentine, talc, diatomaceous earth and other mineral substances Examples thereof include carriers, inorganic salts such as sulfates, nitrates and chlorides, inorganic carriers such as synthetic carriers such as silica, and organic carriers such as sugars, starch, dextrin, wheat flour, soybean flour, corn flour and wood flour. These solid carriers for preparation are usually contained in the agricultural chemical solid preparation of the present invention in an amount of 1 to 90% by weight, preferably 20 to 7%.
Contains 0% by weight.

【0004】本発明の農薬固形製剤は、さらに必要によ
り各種の農薬製剤用補助剤を含有しても良く、該製剤用
補助剤としては、界面活性剤、色素、香料、公知の安定
化剤等が挙げられ、これらは本発明の農薬固形製剤中
に、通常0.1〜35重量%、好ましくは2〜10重量
%含有される。界面活性剤としては、例えばラウリル硫
酸ナトリウムなどのアルキル硫酸エステル塩、アルキル
ナフタレンスルホン酸ナトリウムなどのアルキルアリー
ルスルホン酸塩、リグニンスルホン酸ナトリウムなどの
リグニンスルホン酸塩、コハク酸エステル誘導体、ポリ
エチレングリコールアルキルアリールエーテル硫酸エス
テル塩、芳香族スルホン酸塩のホルムアルデヒド縮合物
等のアニオン性界面活性剤、ポリオキシエチレンアルキ
ルエーテル、ポリオキシエチレンアルキルアリールエー
テル、ポリオキシエチレンアリールアリールエーテル等
のノニオン性界面活性剤が挙げられる。尚、本発明の農
薬固形製剤は、さらに他の農薬活性成分、例えばフェン
プロパトリン、フェンバレレート等のピレスロイド化合
物などを含有してもよい。
The agricultural chemical solid preparation of the present invention may further contain various kinds of auxiliary agents for agricultural chemical preparations, such as surfactants, dyes, fragrances, known stabilizers and the like. And 0.1 to 35% by weight, preferably 2 to 10% by weight, in the solid agricultural chemical preparation of the present invention. Examples of the surfactant include alkylsulfate salts such as sodium lauryl sulfate, alkylarylsulfonates such as sodium alkylnaphthalenesulfonate, ligninsulfonates such as sodium ligninsulfonate, succinate derivative, polyethylene glycol alkylaryl. Examples include anionic surfactants such as ether sulfate ester salts and formaldehyde condensates of aromatic sulfonates, and nonionic surfactants such as polyoxyethylene alkyl ethers, polyoxyethylene alkylaryl ethers, and polyoxyethylene arylaryl ethers. To be The pesticide solid preparation of the present invention may further contain other pesticide active ingredients, for example, pyrethroid compounds such as fenpropatorin and fenvalerate.

【0005】本発明の農薬固形製剤は、(a)アセフェ
ート、(b)酸化硼素および/またはメタ硼酸、(c)
製剤用固形担体、さらに必要により界面活性剤などを加
え、ミキサーなどで混合し、エアーミル、ハンマーミ
ル、遠心式粉砕機などの粉砕機で粉砕したり、これらの
粉砕物をさらにローラーコンパクターなどの圧縮成型
機、押出造粒機、転動造粒機を用いて顆粒状に成型する
等の通常の方法により製造される。
The agricultural chemical solid preparation of the present invention comprises (a) acephate, (b) boron oxide and / or metaboric acid, and (c).
A solid carrier for the formulation, if necessary, a surfactant, etc. are added, mixed with a mixer, etc., and crushed with a crusher such as an air mill, a hammer mill, a centrifugal crusher, or the crushed product is further compressed with a roller compactor, etc. It is produced by a usual method such as molding into granules using a molding machine, an extrusion granulator, or a rolling granulator.

【0006】[0006]

【実施例】以下、本発明を製剤例および試験例を挙げて
より詳細に説明するが、本発明は以下の例のみに限定さ
れるものではない。 製剤例1 アセフェート50重量部、酸化硼素5重量部およびウェ
ッサロンS(デグサ製合成珪酸)45重量部をミキサー
で混合した後、遠心式粉砕機で微粉砕し、本発明の農薬
固形製剤である水和剤を得る。 製剤例2 アセフェート50重量部、酸化硼素5重量部およびトク
シールGU−N(徳山曹達製合成珪酸)45重量部をミ
キサーで混合した後、遠心式粉砕機で微粉砕し、本発明
の農薬固形製剤である水和剤を得る。 製剤例3 アセフェート50重量部、酸化硼素5重量部およびハイ
シール233(PPG製合成珪酸)45重量部をミキサ
ーで混合した後、遠心式粉砕機で微粉砕し、本発明の農
薬固形製剤である水和剤を得る。 製剤例4 アセフェート25重量部、酸化硼素10重量部および硫
酸アンモニウム65重量部をミキサーで混合した後、遠
心式粉砕機で微粉砕し、本発明の農薬固形製剤である水
和剤を得る。
The present invention will be described in more detail below with reference to formulation examples and test examples, but the present invention is not limited to the following examples. Formulation Example 1 50 parts by weight of acephate, 5 parts by weight of boron oxide, and 45 parts by weight of Wessalon S (synthetic silicic acid manufactured by Degussa) were mixed with a mixer and then finely pulverized with a centrifugal pulverizer to obtain the solid pesticide formulation of the present invention. Obtain a wettable powder. Formulation Example 2 50 parts by weight of acephate, 5 parts by weight of boron oxide and 45 parts by weight of Tokusil GU-N (synthetic silicic acid manufactured by Tokuyama Soda) were mixed with a mixer, and then finely pulverized with a centrifugal pulverizer, and the pesticide solid formulation of the present invention To obtain a wettable powder. Formulation Example 3 50 parts by weight of acephate, 5 parts by weight of boron oxide, and 45 parts by weight of Hi-Seal 233 (synthetic silicic acid made by PPG) were mixed by a mixer, and then finely pulverized by a centrifugal pulverizer to prepare water as the pesticide solid formulation of the present invention. Get the remedy. Formulation Example 4 25 parts by weight of acephate, 10 parts by weight of boron oxide and 65 parts by weight of ammonium sulfate are mixed in a mixer and then finely pulverized by a centrifugal pulverizer to obtain a wettable powder which is a solid pesticide formulation of the present invention.

【0007】製剤例5 アセフェート75重量部、酸化硼素10重量部および硫
酸アンモニウム15重量部をミキサーで混合した後、遠
心式粉砕機で微粉砕し、本発明の農薬固形製剤である水
和剤を得る。 製剤例6 アセフェート25重量部、酸化硼素5重量部、ドデシル
ベンゼンスルホン酸ナトリウム5重量部および珪藻土6
5重量部をミキサーで混合した後、遠心式粉砕機で微粉
砕し、本発明の農薬固形製剤である水和剤を得る。 製剤例7 アセフェート40重量部、メタ硼酸10重量部、硫酸ア
ンモニウム10重量部およびハイシール233(前出)
40重量部をミキサーで混合した後、遠心式粉砕機で微
粉砕し、本発明の農薬固形製剤である水和剤を得る。
Formulation Example 5 75 parts by weight of acephate, 10 parts by weight of boron oxide and 15 parts by weight of ammonium sulfate are mixed in a mixer and then finely pulverized by a centrifugal pulverizer to obtain a wettable powder which is a solid agricultural chemical formulation of the present invention. . Formulation Example 6 25 parts by weight of acephate, 5 parts by weight of boron oxide, 5 parts by weight of sodium dodecylbenzenesulfonate and 6 parts of diatomaceous earth
After mixing 5 parts by weight with a mixer, the mixture is finely pulverized with a centrifugal pulverizer to obtain a wettable powder which is the agricultural chemical solid preparation of the present invention. Formulation Example 7 40 parts by weight of acephate, 10 parts by weight of metaboric acid, 10 parts by weight of ammonium sulfate and Hi-Seal 233 (supra)
After mixing 40 parts by weight with a mixer, it is finely pulverized with a centrifugal pulverizer to obtain a wettable powder which is the agricultural chemical solid preparation of the present invention.

【0008】試験例1 製剤例1、2および3で得られた水和剤を50ml容ガラ
ス製アンプルに封入して60℃の恒温器中で2週間保存
した。ガスクロマトグラフィーを用いて、保存前後の製
剤中のアセフェート含量を測定し、その分解率を次式に
より求めた。
Test Example 1 The wettable powders obtained in Formulation Examples 1, 2 and 3 were sealed in a 50 ml glass ampoule and stored in a thermostat at 60 ° C. for 2 weeks. The content of acephate in the preparation before and after storage was measured using gas chromatography, and the decomposition rate was determined by the following formula.

【数1】 また、製剤例1、2および3において、酸化硼素5重量
部に代えてウェッサロンS、トクシールGU−Nまたは
ハイシール233を5重量部用いて同様に製剤した比較
製剤1、2および3についても同様に分解率を求めた。
結果を表1に示す。
[Equation 1] The same applies to Comparative Formulations 1, 2 and 3 prepared in the same manner as in Formulation Examples 1, 2 and 3 using 5 parts by weight of Wesalone S, Tokusil GU-N or Hi-Seal 233 instead of 5 parts by weight of boron oxide. The decomposition rate was calculated.
The results are shown in Table 1.

【0009】[0009]

【表1】 [Table 1]

【0010】試験例2 製剤例4および5で得られた水和剤を50ml容ガラス製
アンプルに封入して60℃の恒温器中で2週間保存し
た。ガスクロマトグラフィーを用いて、保存前後の製剤
中のアセフェート含量を測定し、その分解率を上記式に
より求めた。また、製剤例4および5において、酸化硼
素10重量部に代えて硫酸アンモニウムを10重量部用
いて同様に製剤した比較製剤4および5についても同様
に分解率を求めた。結果を表2に示す。
Test Example 2 The wettable powders obtained in Formulation Examples 4 and 5 were enclosed in a 50 ml glass ampoule and stored in a thermostat at 60 ° C. for 2 weeks. The content of acephate in the preparation before and after storage was measured using gas chromatography, and the decomposition rate was determined by the above formula. Further, in Preparation Examples 4 and 5, the decomposition rate was similarly obtained for Comparative Preparations 4 and 5 prepared in the same manner by using 10 parts by weight of ammonium sulfate instead of 10 parts by weight of boron oxide. The results are shown in Table 2.

【表2】 [Table 2]

【0011】試験例3 製剤例6で得られた水和剤を50ml容ガラス製アンプル
に封入して60℃の恒温器中で2週間保存した。ガスク
ロマトグラフィーを用いて、保存前後の製剤中のアセフ
ェート含量を測定し、その分解率を上記式により求め
た。また、製剤例6において、酸化硼素5重量部に代え
て珪藻土を5重量部用いて同様に製剤した比較製剤6に
ついても同様に分解率を求めた。結果を表3に示す。
Test Example 3 The wettable powder obtained in Preparation Example 6 was enclosed in a 50 ml glass ampoule and stored in a thermostat at 60 ° C. for 2 weeks. The content of acephate in the preparation before and after storage was measured using gas chromatography, and the decomposition rate was determined by the above formula. Further, the degradation rate was similarly obtained for Comparative Preparation 6 prepared in the same manner as in Preparation Example 6, except that 5 parts by weight of diatomaceous earth was used instead of 5 parts by weight of boron oxide. The results are shown in Table 3.

【表3】 [Table 3]

【0012】試験例4 製剤例7で得られた水和剤を50ml容ガラス製アンプル
に封入して60℃の恒温器中で2週間保存した。ガスク
ロマトグラフィーを用いて、保存前後の製剤中のアセフ
ェート含量を測定し、その分解率を上記式により求め
た。また、製剤例7において、メタ硼酸または酸化アル
ミニウム10重量部に代えてハイシール233を10重
量部用いて同様に製剤した比較製剤7についても同様に
分解率を求めた。結果を表4に示す。
Test Example 4 The wettable powder obtained in Preparation Example 7 was enclosed in a 50 ml glass ampoule and stored in a thermostat at 60 ° C. for 2 weeks. The content of acephate in the preparation before and after storage was measured using gas chromatography, and the decomposition rate was determined by the above formula. Further, the degradation rate was similarly determined for Comparative Preparation 7 prepared in the same manner as in Preparation Example 7, except that 10 parts by weight of Hi-Seal 233 was used instead of 10 parts by weight of metaboric acid or aluminum oxide. The results are shown in Table 4.

【表4】 [Table 4]

【0013】[0013]

【発明の効果】本発明は、酸化硼素および/またはメタ
硼酸の添加により、アセフェート原体またはアセフェー
トを含有する農薬固形製剤中のアセフェートの保存安定
性が改善されてなるものである。
INDUSTRIAL APPLICABILITY According to the present invention, the storage stability of acephate in an acephate drug substance or an agrochemical solid preparation containing acephate is improved by adding boron oxide and / or metaboric acid.

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】(a)アセフェート、(b)酸化硼素およ
び/またはメタ硼酸および(c)製剤用固形担体を含有
することを特徴とする農薬固形製剤。
1. A solid agricultural chemical preparation comprising: (a) acephate, (b) boron oxide and / or metaboric acid, and (c) a solid carrier for the preparation.
【請求項2】(a)アセフェート、(b)酸化硼素およ
び(c)製剤用固形担体を含有することを特徴とする農
薬固形製剤。
2. A solid agricultural chemical formulation comprising (a) acephate, (b) boron oxide and (c) solid carrier for formulation.
【請求項3】(a)アセフェート、(b)メタ硼酸およ
び(c)製剤用固形担体を含有することを特徴とする農
薬固形製剤。
3. A solid agricultural chemical preparation comprising: (a) acephate, (b) metaboric acid, and (c) solid carrier for preparation.
【請求項4】アセフェートを含有する農薬固形製剤に、
酸化硼素および/またはメタ硼酸を添加することを特徴
とするアセフェートの安定化方法。
4. A solid agricultural chemical preparation containing acephate,
A method for stabilizing acephate, which comprises adding boron oxide and / or metaboric acid.
【請求項5】酸化硼素および/またはメタ硼酸が添加さ
れてなる安定化されたアセフェート。
5. A stabilized acephate obtained by adding boron oxide and / or metaboric acid.
JP14495493A 1993-06-16 1993-06-16 Agrichemical solid formulation Pending JPH072608A (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
JP14495493A JPH072608A (en) 1993-06-16 1993-06-16 Agrichemical solid formulation
TW83101529A TW296971B (en) 1993-06-16 1994-02-22
FR9403328A FR2706247B1 (en) 1993-06-16 1994-03-22 Method for stabilizing pesticidal compositions containing acephate, and pesticidal compositions obtained.
KR1019940006604A KR950000027A (en) 1993-06-16 1994-03-30 Pesticide composition
US08/220,882 US6335026B1 (en) 1993-06-16 1994-03-31 Pesticidal compositions
ITRM940217A IT1272208B (en) 1993-06-16 1994-04-15 PESTICIDE COMPOSITIONS.
EP94302727A EP0629346A3 (en) 1993-06-16 1994-04-18 Pesticidal compositions.
BR9401546A BR9401546A (en) 1993-06-16 1994-04-19 Process for stabilizing a solid pesticidal composition and the obtained solid pesticidal composition
ES09400807A ES2094681B1 (en) 1993-06-16 1994-04-19 PESTICIDE COMPOSITIONS
CN94104296A CN1096628A (en) 1993-06-16 1994-04-20 Composition pesticide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14495493A JPH072608A (en) 1993-06-16 1993-06-16 Agrichemical solid formulation

Publications (1)

Publication Number Publication Date
JPH072608A true JPH072608A (en) 1995-01-06

Family

ID=15374061

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14495493A Pending JPH072608A (en) 1993-06-16 1993-06-16 Agrichemical solid formulation

Country Status (1)

Country Link
JP (1) JPH072608A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10139607A (en) * 1996-11-08 1998-05-26 Hokko Chem Ind Co Ltd Granular agrochemical wettable agent

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10139607A (en) * 1996-11-08 1998-05-26 Hokko Chem Ind Co Ltd Granular agrochemical wettable agent

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