JPS588003A - Preparation of dust blended with agricultural chemical - Google Patents

Preparation of dust blended with agricultural chemical

Info

Publication number
JPS588003A
JPS588003A JP56103946A JP10394681A JPS588003A JP S588003 A JPS588003 A JP S588003A JP 56103946 A JP56103946 A JP 56103946A JP 10394681 A JP10394681 A JP 10394681A JP S588003 A JPS588003 A JP S588003A
Authority
JP
Japan
Prior art keywords
component
premix
carrier
powder
insecticidal
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
JP56103946A
Other languages
Japanese (ja)
Other versions
JPS64361B2 (en
Inventor
Hiromichi Shimizu
清水 宏道
Akihiko Kunitomo
国友 昭彦
Toshiie Nakamura
中村 利家
Hideaki Tsuji
英明 辻
Katsuhiro Fujita
藤田 勝大
Yukiyoshi Takahi
高日 幸義
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.)
Sankyo Co Ltd
Original Assignee
Sankyo 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 Sankyo Co Ltd filed Critical Sankyo Co Ltd
Priority to JP56103946A priority Critical patent/JPS588003A/en
Publication of JPS588003A publication Critical patent/JPS588003A/en
Publication of JPS64361B2 publication Critical patent/JPS64361B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:In blending the titled dust comprising a votalile germicidal component with an insecticidal component with an adsorbing carrier for preventing the volatility of the germicidal component, to prevent the reduction in effect of the insecticidal component, by blending the dust with the insecticidal component as a premix of it and a specific adsorbing carrier. CONSTITUTION:A premix or dust obtained by blending a volatile germicidal component such as 3-hydroxy-5-methylisoquinazole, etc. effective for controlling sheath blight of rice plant, etc. with an adsorbing carrier (preferably acid clay, or activated clay) for preventing the volatility of the germicidal component is blended with a premix obtained by blending an insecticidal component such as organic phosphorus compound with an adsorbing carrier (especially white carbon, for not causing the reduction in its effect, and, if necessary, a carrier, to give blended dust which prevents the reduction in the effect caused by the volatility of the germicidal component, preventing the reduction in the effect of the blended insecticidal component as well. Preferably the premix of the germicidal component and the premix of the insecticidal component are blended with the carrier, to give the dust.

Description

【発明の詳細な説明】 本発明は揮散性殺菌成分と殺虫成分との農薬混合粉剤の
製法、に関し、茎葉等への散布時に揮散性殺菌成分が揮
散して効力が低下することを防ぐと共に、それに配合さ
れた殺虫成分の効力も低下しない混合粉剤を得ることを
目的とするものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing an agrochemical mixed powder containing a volatile bactericidal component and an insecticidal component, which prevents the volatile bactericidal component from volatilizing and reducing the efficacy when spraying on foliage, etc. The object of the present invention is to obtain a mixed powder that does not reduce the efficacy of the insecticidal ingredients blended therein.

殺菌成分は茎葉表面またはじよじよに内部に取)込まれ
て菌体に作用する良め、茎葉上に極力長期間保持される
ことが好ましいが、−場での効力が劣るものの主要因の
1つとして化合物が揮散してしまう鳩舎がある。そこで
揮散性殺菌成分の製剤化に際しては揮散を抑制してかつ
効果を最大限に発揮させることが必l!である。
It is preferable that the bactericidal component be retained on the foliage for as long as possible so that it can be absorbed into the surface of the foliage or gradually into the interior of the foliage and act on the bacterial cells. One example of this is a pigeon house where the compound volatilizes. Therefore, when formulating volatile sterilizing ingredients, it is essential to suppress volatilization and maximize effectiveness! It is.

最も実用的な手段は揮散性殺菌成分を例えば酸性白土の
ような吸着性担体と混合して揮散を抑制することが考え
られる。しかしながら、殺虫成分を酸性白土等で製剤化
し九場合は殺虫効力は著しく低下してしまう。これは殺
虫成分にあっては最大効果を発揮するためにはある楊変
のすみやかな放出あるいはガス効果が期待されるからで
ある。
The most practical means is to suppress volatilization by mixing volatile sterilizing components with an adsorbent carrier such as acid clay. However, when the insecticidal ingredient is formulated with acid clay or the like, the insecticidal efficacy is significantly reduced. This is because insecticidal ingredients are expected to be released quickly or have a gas effect in order to achieve maximum effectiveness.

ところで、最近は散布の省力化の目的で殺菌成分と殺虫
成分を配合した粉剤が用いられることが多いので、揮散
性殺菌成分と殺虫成分とが共存してもそれぞ謹効果を充
分発現しつる配合粉剤の製造が望まれる。
Incidentally, recently, powders containing bactericidal and insecticidal ingredients are often used for the purpose of saving labor in spraying, so even if volatile bactericidal and insecticidal ingredients coexist, each will still be fully effective. Production of blended powders is desired.

成分の効力低下をsPCすが、殺虫成分をあらかじめ特
定な方法でプレミックスとしてのち配合した場合には、
最終粉剤において均等化されるにもかかわらず、殺虫成
分は酸性白土等への再拡散による影響をほとんどうけず
に充分に効力を発揮することを見い出した。
sPC reduces the effectiveness of ingredients, but if insecticidal ingredients are premixed using a specific method and then later blended,
It has been found that although the insecticidal components are equalized in the final powder, they are hardly affected by re-diffusion into acid clay and the like, and exhibit sufficient efficacy.

本発明の方法は、揮散性殺菌成分をその揮散を防ぎうる
吸着性担体と混合し九プレミックスま九は粉剤と、殺虫
成分をその効力低下をおこさない吸着性担体と混合した
プレミックスとを、必要ならば担体と共に混合して農薬
混合粉剤を製造する方法である。
The method of the present invention uses a premix containing a volatile fungicidal component mixed with an adsorbent carrier capable of preventing its volatilization, and a premix containing a dust powder, and a premix containing an insecticidal component mixed with an adsorptive carrier that does not reduce its efficacy. This is a method of manufacturing an agrochemical mixed powder by mixing with a carrier if necessary.

本発明において、揮散性殺菌成分とは茎葉散布時に揮散
によって効力の低下をきたすなど効果が不安定となるも
のであり、おおよそ20℃における蒸気圧が1×1・ 
■Hf以上のものである。このような殺菌成分としては
、例えば稲紋枯病等の防除に有効な3−ヒドロキシ−S
−メチルイソキサゾール(一般名 ヒメキサゾール)、
野菜のえき病等の防除に有効な5−エトキシ−3−トリ
クロロメチル−も2.4−チアジアゾール(一般名 ニ
トリジアゾール)、稲いもち病等の防除に有効な4−ク
ロロ−3−メチル−ベンゾチアゾール−2−オン(CM
II?)などがあげられる。
In the present invention, a volatile bactericidal component is one whose effectiveness is unstable, such as a decrease in efficacy due to volatilization during spraying on foliage, and whose vapor pressure at approximately 20°C is 1×1.
■It is more than Hf. Such fungicidal components include, for example, 3-hydroxy-S, which is effective in controlling rice sheath blight, etc.
-Methylisoxazole (generic name Himexazole),
5-ethoxy-3-trichloromethyl-, which is effective in controlling vegetable blight, etc., is also 2,4-thiadiazole (generic name: nitridiazole), and 4-chloro-3-methyl-, which is effective in controlling rice blast, etc. Benzothiazol-2-one (CM
II? ) etc.

殺虫成分はある程度揮散性が高いものでも低いものでも
よく、とくに限定されないが、例えば&O−ジメチル0
−(S−メチル−4−二トロフェニル)チオホスフェー
ト(フェニトロチオン)、LO−ジエチル 0−(S−
フェニル−3−インキサゾリル)ホスホロチオエート(
インキサチオン)、亀・−ジメチル $−(3−メチル
−4−メチルチオフェニル)チオホスフェート(フェン
チオン)、(L(1−ジメチル0−〔2−クロロ−1−
(2,4−ジクロロフェニル)ビニル〕ホスフェート(
ジメチルビンホス)、エチル α−(へ0−ジメチル−
ジチオホスホリル)フェニルアセテート(フエントエー
ト)、へO−ジ−n−プロピル @−(4−メチルチオ
フェニル)ホスフェート(プロパホス)のような有機リ
ン化合物;1−ナフチルN−メチルカーバメート(カル
バリル)、m−トリルN−メチルカーバメート(MテM
、O)、λ4−キシリルに一メチルカーバメート(MP
MO)、λ5−キシリルN−メチルカーバメート(nt
c)、2−5ea−ブチルフェニル夏−メチルヵーパメ
−) (BPMC)のようなカーバメート化合物:パー
メスリン、レスメスリン、フェンバレレートのようなピ
レスロイド化合物があげられる。
The insecticidal component may have high or low volatility to a certain extent, and is not particularly limited, but for example, &O-dimethyl 0
-(S-Methyl-4-nitrophenyl)thiophosphate (fenitrothion), LO-diethyl 0-(S-
phenyl-3-inxazolyl) phosphorothioate (
inxathion), tortoise-dimethyl $-(3-methyl-4-methylthiophenyl)thiophosphate (fenthion), (L(1-dimethyl0-[2-chloro-1-
(2,4-dichlorophenyl)vinyl]phosphate (
dimethylvinphos), ethyl α-(h0-dimethyl-
Organophosphorus compounds such as dithiophosphoryl)phenylacetate (fuentate), O-di-n-propyl@-(4-methylthiophenyl)phosphate (propaphos); 1-naphthyl N-methylcarbamate (carbaryl), m-tolyl N-methyl carbamate (MteM
, O), λ4-xylyl monomethyl carbamate (MP
MO), λ5-xylyl N-methylcarbamate (nt
c) Carbamate compounds such as 2-5ea-butylphenyl-methylcarpame-) (BPMC); Examples include pyrethroid compounds such as permethrin, resmethrin, and fenvalerate.

揮散性殺菌成分の揮散を防ぎうる吸着性担体は、揮散性
殺菌成分の蒸気を充分に吸着しつるものであればよく、
例えばモンモリロナイト系粘土吸着剤である酸性白土、
活性白土、ベントナイトなどが用いられる。とくに酸性
白土シよび活性白土のような静電的に活性な吸着能を有
するもの状好適に用いられる。またベントナイトは酸性
に不安定な主剤に用いられる。このような吸着性担体の
所用量拡、揮発性殺菌成分の物理化学的性状および担体
の吸着能によって異なるが、酸性白土、活性白土O楊合
祉過常最終粉剤中に20−以上好ましくL4$−以上を
含ませることによって目的を達する。この担体は揮散性
殺菌成分のプレミックスま九鉱粉剤の製造時に配合する
か、不足分は彼の混合工横で配合してもよい。
The adsorbent carrier capable of preventing volatilization of the volatile sterilizing component may be one that can sufficiently adsorb the vapor of the volatile sterilizing component,
For example, acid clay, which is a montmorillonite clay adsorbent,
Activated clay, bentonite, etc. are used. In particular, materials having electrostatically active adsorption ability such as acid clay and activated clay are preferably used. Bentonite is also used as a base ingredient that is unstable to acids. Although it varies depending on the required amount of the adsorbent carrier, the physicochemical properties of the volatile bactericidal component, and the adsorption capacity of the carrier, the amount of acid clay, activated clay, and activated clay in the final powder is preferably 20 or more L4$- or more. Achieve your goal by including. This carrier may be added at the time of manufacturing the volatile fungicidal premix powder, or the missing amount may be added at the mixer's side.

殺虫成分のプレミックスを製造する丸めの吸着性担体は
、比表面積が大きいいわゆる高吸油能の吸着性担体であ
り、前記揮散性殺菌成分のために用いられる吸着性担体
とは別のものであって、殺虫成分と混合しても効力低下
をおこさないものであればよい。このような吸着性担体
としては例えば、ホワイトカーボン、珪藻土−1軽石の
微粉末、天然または合成のゼオライト、シリカゲルが用
いられる。とくにホワイトカーボンは合成された含水け
い酸、含水けい酸塩または無水けい酸の種類があシ、水
中で酸性、中性またはアルカリ性を呈するものがあるが
、いずれも好適に使用でき、主剤に応じて最も適当なも
のが選択される。殺虫成分のプレミックスを製造するに
際してこのような吸着性担体の所用量は、殺虫成分1部
に対してaSS部上上好ましくは1部以上が用いられる
The round adsorbent carrier for producing the premix of insecticidal ingredients is a so-called high oil absorption adsorbent carrier with a large specific surface area, and is different from the adsorbent carrier used for the volatile bactericidal ingredient. Any substance may be used as long as it does not cause a decrease in efficacy even when mixed with insecticidal ingredients. Examples of such adsorptive carriers include white carbon, diatomaceous earth-1 pumice powder, natural or synthetic zeolite, and silica gel. In particular, white carbon can be synthesized in the form of hydrated silicic acid, hydrated silicate, or anhydrous silicic acid, and can be acidic, neutral, or alkaline in water. The most appropriate one is selected. When producing a premix of the insecticidal component, the amount of adsorbent carrier used is preferably 1 part or more based on the aSS part per 1 part of the insecticidal component.

上記以外の増量の目的で配合される担体は、通常粉剤の
製造に用いられるもの、例えばタルク、クレー、炭酸カ
ルシウム(重質)などが用いられる。
The carriers used for the purpose of increasing the amount other than those mentioned above are those commonly used in the production of powders, such as talc, clay, and calcium carbonate (heavy).

揮散性殺菌成分または殺虫成分と上記吸着、性担体とを
混合するには、主剤が常温で固体の原体である場合は主
剤と担体を混合粉砕するか、固体原体を加温法Mまたは
溶媒に溶解して液状化し、これを担体に混合吸着する。
To mix the volatile bactericidal component or insecticidal component with the above-mentioned adsorptive or active carrier, if the base ingredient is a solid raw material at room temperature, the base ingredient and carrier may be mixed and pulverized, or the solid raw material may be mixed with heating method M or It is dissolved in a solvent and liquefied, and mixed and adsorbed onto a carrier.

主剤が常温で液状の原体である場合は通常そのま\用い
るが、必要に応じ溶媒に溶解してこれを担体に混合吸着
する。これらの溶媒を用いた場合に、低沸点溶媒は製造
工程中で回収することができ、高沸点溶媒は製剤中にそ
のま\共存させてもよい。
When the main ingredient is a raw material that is liquid at room temperature, it is usually used as is, but if necessary, it is dissolved in a solvent and mixed and adsorbed onto a carrier. When these solvents are used, the low boiling point solvent can be recovered during the manufacturing process, and the high boiling point solvent may be allowed to coexist in the formulation as is.

本発明の混合粉剤を製造する態様として祉、揮散性殺菌
成分のプレミックスと殺虫成分のプレミックスとを担体
と共に混合粉砕する方法が最も好ましいが、他に揮散性
殺菌成分のプレミックスと担体とを混合粉砕して粉剤を
製造し、これに殺虫成分のプレミックスを混合する方法
、殺虫成分のプレミックスと担体とを混合粉砕して粉剤
を製造し、これに揮散性殺菌成分のプレミックスを混合
する方法、揮散性殺菌成分をその揮散を防ぎうる吸着性
担体と混合粉砕して粉剤を製造し、これに殺虫成分のプ
レミックスを混合してもよい。ようするに殺虫成分はプ
レミックスを用いることが必須であるが、揮散性殺菌成
分はプレミックスでも粉剤でもよく、他の担体とは適宜
の段階で混合されつる。
The most preferable method for producing the mixed powder of the present invention is to mix and pulverize a premix of volatile sterilizing ingredients and a premix of insecticidal ingredients together with a carrier. A method in which a premix of insecticidal ingredients is mixed with a premix of an insecticidal ingredient, and a premix of an insecticidal ingredient is mixed with a carrier to produce a powder, and a premix of a volatile sterilizing ingredient is added to this. As for the mixing method, a powder may be prepared by mixing and pulverizing a volatile fungicidal component with an adsorbent carrier capable of preventing its volatilization, and a premix of the insecticidal component may be mixed into this powder. In this way, it is essential to use a premix for the insecticidal component, but the volatile fungicidal component may be a premix or a powder, and is mixed with other carriers at an appropriate stage.

また前述したように、揮散性殺菌成分の揮散を防ぐため
の担体の不足分は後の混合工程の適宜の段階で追加して
もよい。
Furthermore, as described above, the amount of carrier needed to prevent volatilization of volatile sterilizing components may be added at an appropriate stage of the subsequent mixing step.

なお、製造の適宜の段階で安定剤、物理性改良剤などの
助剤を配合することができることはいうまでもない。
It goes without saying that auxiliary agents such as stabilizers and physical property improvers can be added at appropriate stages of production.

以下に本発明の混合粉剤の製造実施例および試験例をあ
げ説明する。
Production examples and test examples of the powder mixture of the present invention will be described below.

実施例1゜ ヒメキサゾールプレミックス〔ヒメキサゾール原体(9
89G ) 40.1部と酸性白土51L2部の混合粉
砕品345部に、フェニトロチオンプレミックス〔フェ
ニトロチオン原体(96,5% ) 41.5部とホワ
イトカーボン5ILS部の混合粉砕品〕4s部を加えて
ハンマーミルで粉砕混合し、さらにクレー3&0部およ
び酸性白土SU部を加え攪拌混合して粉剤を得た。
Example 1 Hymexazole premix [hymexazole drug substance (9
To 345 parts of a pulverized mixture of 40.1 parts of 89G) and 2 parts of acid clay 51L, 4s parts of fenitrothion premix [pulverized mixture of 41.5 parts of fenitrothion raw material (96.5%) and 5ILS of white carbon] was added. The mixture was ground and mixed in a hammer mill, and 3&0 parts of clay and SU parts of acid clay were added and mixed with stirring to obtain a powder.

実施例2 ヒメキサゾールプレミックス〔ヒメキサゾール原体C@
8%>L2部を塩化メチレンLO部に溶解させ、酸性白
土SO,O部に吸着混合後塩化メチレンを揮散させ丸も
の)512部に、インキサチオンプレミックス〔インキ
サチオン原体(11fk ) 440部とホワイトカー
ボン5&o部の混合粉砕品345部を加えハンマーミル
で粉砕混合し、さらにクレー4LSgを加え攪拌混合し
て粉剤を得え。
Example 2 Hymexazole premix [hymexazole bulk C@
8%>L2 part was dissolved in LO part of methylene chloride, adsorbed and mixed with acidic clay SO, O part, and the methylene chloride was volatilized to make 512 parts of inxathion premix [inxathion raw material (11fk) 440 parts Add 345 parts of a pulverized mixture of 5 & o parts of white carbon and pulverize with a hammer mill, then add 4LSg of clay and mix with stirring to obtain a powder.

実施例i ヒメキサゾールプレミックス(実施例1と同一品)!L
!1部に、MTMOプレミックス〔M丁MO原体(SS
%)12部を塩化メチレン龜・部に溶解させホワイトカ
ーボンーロ部KIl1着混合しハンマーミルで粉砕後塩
化メチレンを揮散させたもの〕77.2部クレーS1.
3部および酸性白土5Q、1部を加え攪拌混合して粉剤
を得九。
Example i Hymexazole premix (same product as Example 1)! L
! Part 1 contains MTMO premix [MTMO original material (SS
%) was dissolved in methylene chloride solution, mixed with white carbon and mixed with 1 part of methylene chloride, crushed in a hammer mill, and the methylene chloride was volatilized] 77.2 parts of clay S1.
Add 3 parts and 1 part of acid clay 5Q and mix with stirring to obtain a powder.

実施例4゜ ヒメキサゾールプレミックス(実施例2と同一品) 5
42部に、M?MOプレミックス(実施例3と同一品)
1.2部を加え同様に粉砕混合し、さらにクレー4a@
部を加え攪拌混合して粉剤を得た。
Example 4 Hymexazole premix (same product as Example 2) 5
M in the 42nd part? MO premix (same product as Example 3)
Add 1.2 parts, grind and mix in the same way, and then add clay 4a@
1 part and stirred and mixed to obtain a powder.

実施例i ニトリジアゾールプレミックス〔ニトリジアゾール原体
(95% ) 27.1部と酸性白土71部の混合粉砕
品) 11.0部に、クレー331石部および酸性白土
5ILI部を加え同様に粉砕混合後、BPMOフレミッ
クス[BPMOi体(11,5% ) 404部とホワ
イトカーボン5ILJ部の混合粉砕品〕!L5部を加え
攪拌混合して粉剤を得た。
Example i Nitridiazole premix [mixture pulverized product of 27.1 parts of nitridiazole raw material (95%) and 71 parts of acid clay] To 11.0 parts, 331 parts of clay and 5 ILI parts of acid clay were added and the same procedure was carried out. After pulverization and mixing, BPMO Flemix [mixed pulverized product of 404 parts of BPMOi (11.5%) and 5 ILJ parts of white carbon]! 5 parts of L were added and mixed with stirring to obtain a powder.

実施例1 フェンエートプレミックス〔フェンエート原体〔s16
チ)41.7部とホワイトカーボン513部の混合粉砕
品315部に、クレー3io部および酸性白土sue部
を加え同様に粉砕混合後、ニトリジアゾールプレミック
ス(実施例5と同一品)5.5部を加え攪拌混合して粉
剤を得た。
Example 1 Phenate premix [Phenate raw material [s16]
h) To 315 parts of a mixed pulverized product of 41.7 parts of white carbon and 513 parts of white carbon, 3io parts of clay and sue parts of acid clay were added and mixed in the same manner, followed by nitridiazole premix (same product as in Example 5)5. 5 parts were added and mixed with stirring to obtain a powder.

実施例7゜ CMBTプレミックス((!MBτ原体(Its % 
)41.5部と酸性白土515部の粉砕混合品〕4s部
とフェニトロチオンプレミックス(実施例1と同一品)
45部に、クレー89部および酸性白土SO,O部を加
え攪拌混合して粉剤を得た。
Example 7゜CMBT premix ((!MBτ bulk (Its %
) 41.5 parts of pulverized mixture of acid clay and 515 parts of acid clay] 4s parts and fenitrothion premix (same product as Example 1)
To 45 parts, 89 parts of clay and parts of acid clay SO,O were added and mixed with stirring to obtain a powder.

実施例東 (:!MB’!原体(96,5% ) l 3部と酸性
白土StO部およびクレー417部を混合粉砕して粉剤
とし、さらにパーメスリンプレミックス〔パーメスリン
原体(s s % ) 2oo部とホワイトカーボン7
7.0部の混合粉砕品〕1.@部を加え粉砕混合して粉
剤管得た。
Example East (:!MB'! Raw material (96.5%) l 3 parts, acid clay StO part and clay 417 parts were mixed and ground to make a powder, and further permethrin premix [permethrin raw material (s s %) ) 2oo part and white carbon 7
7.0 parts of mixed pulverized product] 1. @ part was added and ground and mixed to obtain a powder tube.

実施例1 ヒメキサゾールプレミックス〔ヒメキサゾー施例2と同
一品)tS部およびクレー5tost’混合後ハンマー
ミルで粉砕して粉剤を得た。
Example 1 Hymexazole premix (same product as Hymexazole Example 2) After mixing part tS and 5 tost' of clay, the mixture was ground in a hammer mill to obtain a powder.

実施例1a OMBTプレミックス[: cMBrg体(mis S
 )41.5部と活性白土515部の粉砕混合品35.
5部とイソキサチオンプレミックス〔実施例2と同一品
345部およびクレー89部を混合後ハンマーミルで粉
砕して粉剤を得た。
Example 1a OMBT premix [: cMBrg body (mis S
) and 515 parts of activated clay 35.
5 parts of isoxathion premix [same as in Example 2, 345 parts, and 89 parts of clay were mixed and ground in a hammer mill to obtain a powder.

試験例1゜ 揮散性殺菌成分の揮散抑制試験 実JHICヒメキサゾール)、実施例S(ニトリジアゾ
ール)および実施例7 (CMBr)の方法によって製
造された粉剤について、またそれぞれの処方中の酸性白
土の代りに第1表にかかげる担体を用いた粉剤について
、揮散性殺菌成分の残存率を測定した。
Test Example 1゜Volatilization Suppression Test of Volatile Bactericidal Components Regarding the powders produced by the methods of JHIC hymexazole), Example S (nitridiazole) and Example 7 (CMBr), and the effect of acid clay in each formulation, Instead, the residual rate of volatile sterilizing components was measured for powders using the carriers listed in Table 1.

揮散性試験は粉剤サンプル約5・ダを採夛、標準ふるい
(150メツシユ)の金網上におき、刷毛を使用して約
10amの高さから、5X10Gのスライドグラス上に
できるだけ均一になるように粉剤29〜30〜を散布し
た。このスライドグラスは、あらかじめ60℃、相対湿
度TO%に調整した恒温器内に24時間静置して殺菌成
分を揮散させた後にと9出し、スライドグラス上のサン
プルをアセトンで洗い落し、それぞれの殺菌成分の残存
緻を定量し、初期散布されたサンプル重量から計算によ
り求めた殺菌成分重量に対する残存率を算出した。結果
を表−IK示す。
For the volatility test, take a powder sample of about 5 mm, place it on a wire mesh of a standard sieve (150 mesh), and use a brush to spread it as uniformly as possible onto a 5 x 10 G slide glass from a height of about 10 am. Powders 29-30 were sprayed. This slide glass was placed in a thermostat pre-adjusted to 60°C and relative humidity TO% for 24 hours to volatilize the bactericidal components, and then removed.The sample on the slide glass was washed off with acetone, and each The residual density of the bactericidal component was quantified, and the residual rate was calculated based on the weight of the bactericidal component calculated from the initial sprayed sample weight. The results are shown in Table IK.

第   1   表 本は主剤を塩化メチレンに溶解して担体に吸着させたの
ち塩化メチレンを留去させ丸サンプルを示す。
Table 1 shows a round sample in which the base agent was dissolved in methylene chloride and adsorbed onto a carrier, and then the methylene chloride was distilled off.

第1表から明らかなように、本発明の粉剤における殺菌
成分の揮散性よくおさえられているが、一般担体におき
かえ九粉剤で紘揮散がきわめて大きいことがわかる。
As is clear from Table 1, the volatility of the bactericidal component in the powder of the present invention is well controlled, but when the powder was replaced with a general carrier, the volatility was extremely large.

イネ紋枯病防除実験(保護効果) プラスチック製容器(30X4ScI!、深さ2saM
)中で幼穂形成中期まで育成したイネ(品種=4株 日本晴、/)に、各供試粉剤を小型散 容器 粉器で41.21または1f / 111”の割合で散
布し、温室内に7日間放置した後、紋枯病菌(Psll
icultria 5asakii )を培養したイネ
ワラを地際部の茎にしばりつけ接種した。これを温度2
1〜30℃、湿度90%以上の温室に14日間保存した
後、発病の程fを病斑形成の高さくcll)によって調
査した。1区3連制とし、そO平均値を第2表に示した
。なお、対照粉剤は一般的な粉剤の製造法と同じように
、それぞれの実施例における揮散性膜1M成分と殺虫成
分はプレミックスせす、クレーのみの担体と混合して製
造された粉剤。
Rice sheath blight control experiment (protective effect) Plastic container (30X4ScI!, depth 2saM
) was grown to the middle stage of panicle formation (variety = 4 plants, Nipponbare, /), each test powder was sprinkled at a rate of 41.21 or 1f/111" using a small duster, and 7 After leaving it for a day, sheath blight fungus (Psll)
icultria 5asakii) was tied to the stem at the ground level and inoculated. This temperature 2
After storing for 14 days in a greenhouse at 1 to 30° C. and a humidity of 90% or more, the degree of disease onset was determined by the height of lesion formation (cll). Table 2 shows the average SOO value for each ward of three consecutive races. The control powder is a powder prepared by premixing the volatile film 1M component and the insecticidal component in each example and mixing it with a clay-only carrier in the same way as a general powder production method.

粉剤        2         ″1実施例
3の     4.        αT−粉剤   
      2          t。
Powder 2″1 Example 3 4. αT-Powder
2t.

1          48 実施例10     4         龜■対照粉
剤       2          tsl   
  、    11@ 対照粉剤       2        121  
     2α1 試験例龜 トマトえき病防除実験 プラスチック製容器(30X45cm、深さ2Sdll
)中で6〜1葉期まで育成したトマト(品種:新福寿、
1/容。)に、各供試粉剤を小型散粉器で41.29ま
たは1 j’ /z’の割合で散布し、3日間放置した
後、別に準備したえき病菌(Fhytophthora
 1nfestans)の胞子を噴霧接種した。これを
温度20℃、湿度IQOチ以上の温室に24時間放置し
た彼、25〜27℃湿度8・−以上の温室に移し、5日
後に上位5葉について病斑面積を調査して一葉あたフの
病斑面積率を算出し丸。1区3連制とし、その平均値を
第3表に示した。なお、対照粉剤は試験例2に説明した
ものと同じ。
1 48 Example 10 4 Control powder 2 tsl
, 11@ Control powder 2 121
2α1 Test example Tomato blight control experiment Plastic container (30 x 45 cm, depth 2 Sdll
) grown to the 6-1 leaf stage (variety: Shinpuku Kotobuki,
1/Yong. ) with a small duster at a ratio of 41.29 or 1 j'/z', and after leaving it for 3 days, separately prepared
1 nfestans) spores were spray inoculated. He left the plants in a greenhouse for 24 hours at a temperature of 20℃ and a humidity of over 8 degrees, then moved them to a greenhouse at 25 to 27 degrees Celsius and a humidity of 8. Calculate the area ratio of the lesions and draw a circle. Each ward was divided into three series, and the average values are shown in Table 3. The control powder was the same as that described in Test Example 2.

第   3   表 実施例5の     4          ・粉剤 
        2          。
Table 3 Example 5-4 ・Powder
2.

1          12 実施例6の      40 粉剤         2s I           Is 実施例5の     4        45対照粉剤
       2         7s実施例口の 
    4       51対照粉剤       
2        81無散布       iss 試験例4゜ イネいもち病防除実験 周囲にいもち病(Pyricularla oryma
e )が多発している野外畑晩婚苗代で3〜41Mtで
育成し九イネ(品種:農林2o号)に各供試粉剤を小臘
散粉器で4f、2f″1が3割合で散布し九(いもち病
初発前)。1区15♂、3連制とし、薬剤散布T目抜シ
よび14日後に各区から任意K 180本ずつ抜き取)
上位2葉に形成されている病斑数を調査した。第4表に
は一葉当)平均病斑数を示した。なお、対照粉剤は試験
例2に説明したものと同じ。
1 12 40 powder of Example 6 2s I Is 4 of Example 5 45 Control powder 2 7s Example mouth
4 51 control powder
2 81 No spraying iss Test example 4゜ Rice blast control experiment
e) were grown at 3 to 41 Mt in late-marriage seedlings in an outdoor field, where many cases of 4f and 2f''1 were grown, and each test powder was sprayed with a small duster at a ratio of 4f and 2f''1 to 9 rice (variety: Norin 2o). (Before the first appearance of rice blast disease. 15♂ per area, 3 consecutive times, and 180 arbitrary K were removed from each area after 14 days by removing the chemical spray T)
The number of lesions formed on the top two leaves was investigated. Table 4 shows the average number of lesions per leaf. The control powder was the same as that described in Test Example 2.

第   4   表 実施例1(1)     4          as
    42粉剤        ’l       
   if    &11          1、S
    象S実施例Sの    4         
1.1   45粉剤        2      
   &3   t・1           74 
 1t、2実施例Tの     4         
12  1L2対照粉剤      2       
  &2 2龜4実施例$の     4      
    tl   !45対R粉剤      2  
       tis   2*s無散布      
 ロ4I翫3 上記試験例2〜4の病害防除試験では、本発明の揮散性
殺菌成分を酸性白土と混合して製造された粉剤は対照の
クレーと混合して製造された粉剤に比べ、はるかに薬効
が大きく、揮散による効力低下が少ないことがわかる。
Table 4 Example 1 (1) 4 as
42 powder 'l
if &11 1, S
Elephant S Example S 4
1.1 45 powder 2
&3 t・1 74
1t, 2 Example T 4
12 1L2 control powder 2
&2 2 4 example $4
Tl! 45 vs R powder 2
tis 2*s no spraying
In the disease control tests of Test Examples 2 to 4 above, the powders produced by mixing the volatile fungicidal component of the present invention with acid clay were far more effective than the powders produced by mixing them with the control clay. It can be seen that the medicinal efficacy is high, and the decrease in efficacy due to volatilization is small.

試験例i トビイロウンカ、ツマグロヨコバイ殺虫実験上部内径1
asc*、底内径lG1深さ11)1111Nのプラス
チック製ポットに土壌と水を満して水田状態とし、種苗
(東海17号)を3本植として温室内で育てた。稲がI
Sawg度に生長し九時、ポット上に内径&ScM、高
さ251の透明なプラスチック薄板製円筒を稲Kかぶせ
るように立てた。散粉は市販のエンジンクリーナ(K−
@1゜近畿製作新製、大阪)で、噴出口から1f国の距
離に所定の粉剤を入れた小皿(磁製ルツボのふた、直径
z rx )が乗るように加工したもので行なつ九。こ
れを小皿がポットの水面近(になるまで円筒内に挿入し
、先端から空気を瞬間的に噴出させて(コンプレッサー
圧力ts#/d)、小皿中の粉剤を飛散させ丸。この際
、ウレタンフオームラバーの円板で円筒上部を閉じ良状
態で行ない、粉剤が円筒外にもれるのを防いだ。
Test example I: Brown planthopper and black leafhopper insecticidal experiment Upper inner diameter 1
asc*, bottom inner diameter lG1 depth 11) A 1111N plastic pot was filled with soil and water to form a paddy field, and three seedlings (Tokai No. 17) were planted and grown in a greenhouse. Rice is I
At 9 o'clock, when the rice had grown to Sawg degree, a transparent thin plastic cylinder with an inner diameter of &ScM and a height of 251 cm was placed over the pot to cover the rice. For powder, use a commercially available engine cleaner (K-
@1゜Kinki Seisaku Shin, Osaka), which was processed so that a small plate (porcelain crucible lid, diameter zrx) containing the specified powder was placed at a distance of 1 f from the spout. Insert this into the cylinder until the small plate is close to the water surface of the pot, and then blow out air momentarily from the tip (compressor pressure ts#/d) to scatter the powder in the small plate. The upper part of the cylinder was closed with a foam rubber disk to prevent the powder from leaking out of the cylinder.

その後、供試虫を1ポット当り10頭前後、あらかじめ
円筒内にとシつけた戸紙製のコーン内に放ち、揺上へ自
由に移動させた。円筒にはナイロンコース製の上ぶ+t
−かぶせ、2S1±1℃、16時間照明の室内に保ち、
72時間後の生死判定を行なった。各区のく夛かえしは
2連制とした。結果は第5表および第6表に示す。
Thereafter, about 10 test insects per pot were released into paper cones that had been placed inside the cylinder in advance, and allowed to move freely onto the shaker. The cylinder has a nylon course upper + t
- Cover and keep in a room with lighting at 2S1±1℃ for 16 hours.
After 72 hours, a determination of life or death was made. Each ward will have two consecutive visits. The results are shown in Tables 5 and 6.

なお、対照粉剤Aは、それぞれの実施例における揮散性
殺菌成分のプレミックスに殺虫成分はプレミックスせず
に実施例と同じクレーおよび酸性白土を混合して製造さ
れた粉剤。対照粉剤Bは、一般的な粉剤の製造法と同じ
ように、それぞれの実施例における揮散性殺菌成分と殺
虫成分をいずれもプレミックスせず、クレーのみの担体
と混合して製造された粉剤。対照粉剤Cは、それぞれの
実施例における揮散性殺菌成分と殺菌成分をいずれもプ
レミツゲスせず、酸性白土のみの担体と混合して製造さ
れた粉剤・本発明の粉剤および対照粉剤はいずれも密閉
容器中に40Uで1ケ月保存しえものについて試験した
In addition, control powder A is a powder prepared by mixing the same clay and acid clay as in the example without premixing the insecticidal component with the premix of the volatile bactericidal component in each example. Control powder B is a powder produced by mixing with a clay carrier only, without premixing either the volatile bactericidal component or the insecticidal component in each example, in the same way as in a general powder production method. Control powder C is a powder prepared by mixing the volatile bactericidal component and the bactericidal component in each example with a carrier of only acid clay without premixing.The powder of the present invention and the control powder are both stored in a closed container. A test was conducted on fresh meat that had been stored in 40 U for one month.

第   5   表 トビイロクンカ終令幼虫に対する試験 第   6   表 新和系ツマグロヨコバイ終令幼虫に対する試験上記の第
5,6表から本発明の実施例の粉剤の殺虫効力は、クレ
ーのみを担体とするそれぞれの対照粉剤Bと同等に有効
であった。しかし  ゛この対照粉剤Bは殺菌効力につ
いては第2〜4表に示したように低下した。酸性白土の
みを担体とする対照粉剤Cは殺菌効力は低下しないが、
殺虫効力は著しく低下し倉。tた殺虫成分をプレミック
スせずに配合した対照粉剤ムはや紘)酸性白土の影響を
うけて殺虫効力の低下が著しいO こOように、本発明の粉剤においては、揮散性殺菌成分
の蒸気を酸性白土が吸着するので揮散性が抑制されて充
分な効力を発揮すると共に、ホワイトカーボンに吸着さ
れた殺虫成分はもはや酸性白土の影響をうけて効力が低
下することなく充分な効力を発揮するという優れた効果
がある。
Table 5: Test against the final instar larva of the Japanese black leafhopper Table 6: Test against the final instar larva of the Shinwa black leafhopper From Tables 5 and 6 above, the insecticidal efficacy of the powders of the examples of the present invention is compared to the respective controls using only clay as a carrier. It was equally effective as powder B. However, the bactericidal efficacy of the control powder B was reduced as shown in Tables 2 to 4. Control powder C, which uses only acid clay as a carrier, does not reduce its bactericidal efficacy, but
Insecticidal efficacy is significantly reduced. The control powder, which was formulated without premixing the insecticidal ingredients, showed a significant decrease in insecticidal efficacy due to the influence of acidic clay. As vapor is adsorbed by acid clay, volatility is suppressed and sufficient efficacy is exhibited, and the insecticidal ingredients adsorbed by white carbon are no longer affected by acid clay and exhibit sufficient efficacy. It has an excellent effect.

特詐出願人 三共株式金社 代理人 弁理士樫山庄治Special fraud applicant: Sankyo Co., Ltd. Agent: Patent attorney Shoji Kashiyama

Claims (1)

【特許請求の範囲】 1、 揮散性殺菌成分をその揮散を防ぎうる吸着性担体
と混合したプレミックスを九は粉剤と、殺虫成分をその
効力低下をおこさない吸着性担体と混合したプレミック
スとを、必要ならば担体と共に混合することを特徴とす
る農薬配合粉剤の製法。 2 揮散性殺菌成分のプレミックスと殺虫成分のプレミ
ックスとを、担体と共に混合する特許請求の範囲第1項
記載の製法。 寡 揮散性殺菌成分の担体が瞭性白土または活性白土で
あり、殺虫成分の担体がホワイトカーボンである特許請
求の範囲第1項また社第、2項記載の製法。 未 揮散性殺菌成分が3−ヒドロキシ−5−メチルイン
キサゾール、5−エトキシ−3−トIJ クロロメチル
−t2.3−チアジアゾールま7’tは4−クロロ−3
−メチル−1,3−ベンゾチアゾール−2−オンである
特許請求の範囲第1項記載の製法。 i 殺虫成分が有機リン化合物、カーバメート化合物ま
たはピレスロイド化合物である特許請求の範囲第1項記
載の製法。
[Scope of Claims] 1. A premix in which a volatile bactericidal component is mixed with an adsorbent carrier that can prevent its volatilization, and a premix in which an insecticidal component is mixed with an adsorbent carrier that does not reduce its efficacy. A method for producing an agrochemical compound powder, which comprises mixing the following with a carrier if necessary. 2. The manufacturing method according to claim 1, wherein a premix of a volatile fungicidal component and a premix of an insecticidal component are mixed together with a carrier. The method according to claim 1 or claim 2, wherein the carrier for the low-volatile bactericidal component is clear clay or activated clay, and the carrier for the insecticidal component is white carbon. The non-volatile bactericidal component is 3-hydroxy-5-methylinxazole, 5-ethoxy-3-IJ chloromethyl-t2,3-thiadiazole or 7't is 4-chloro-3
-Methyl-1,3-benzothiazol-2-one. The method according to claim 1, wherein the insecticidal component is an organic phosphorus compound, a carbamate compound, or a pyrethroid compound.
JP56103946A 1981-07-03 1981-07-03 Preparation of dust blended with agricultural chemical Granted JPS588003A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56103946A JPS588003A (en) 1981-07-03 1981-07-03 Preparation of dust blended with agricultural chemical

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56103946A JPS588003A (en) 1981-07-03 1981-07-03 Preparation of dust blended with agricultural chemical

Publications (2)

Publication Number Publication Date
JPS588003A true JPS588003A (en) 1983-01-18
JPS64361B2 JPS64361B2 (en) 1989-01-06

Family

ID=14367599

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56103946A Granted JPS588003A (en) 1981-07-03 1981-07-03 Preparation of dust blended with agricultural chemical

Country Status (1)

Country Link
JP (1) JPS588003A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63189914A (en) * 1987-02-02 1988-08-05 Tlv Co Ltd Pressure regulating device for self adjusting valve

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63189914A (en) * 1987-02-02 1988-08-05 Tlv Co Ltd Pressure regulating device for self adjusting valve
JPH0560611B2 (en) * 1987-02-02 1993-09-02 Tlv Co Ltd

Also Published As

Publication number Publication date
JPS64361B2 (en) 1989-01-06

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