JPH01157903A - Dispersant composition for agricultural chemical wettable powder - Google Patents
Dispersant composition for agricultural chemical wettable powderInfo
- Publication number
- JPH01157903A JPH01157903A JP62318177A JP31817787A JPH01157903A JP H01157903 A JPH01157903 A JP H01157903A JP 62318177 A JP62318177 A JP 62318177A JP 31817787 A JP31817787 A JP 31817787A JP H01157903 A JPH01157903 A JP H01157903A
- Authority
- JP
- Japan
- Prior art keywords
- starch hydrolyzate
- wettable powder
- agricultural chemical
- surfactant
- granular starch
- 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
Links
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
本発明は、水に易溶性の顆粒状農薬水和剤用分散剤組成
物に関するものである。The present invention relates to a dispersant composition for a granular agricultural chemical wettable powder that is easily soluble in water.
(従来の技術)
農薬水和剤は、農薬活性成分、モンモリロナイト等の粘
土鉱物質及び界面活性剤を主成分としたもので、取り扱
いが容易であり、適当な溶剤がないため乳剤化できない
農薬原体あるいは経時的な結晶析出のために流動化でき
ない農薬原体でも利用できるなどの利点があることから
、今日広く用いられている。
以上において、分散剤としてナフタリンスルホン酸ナト
リウム塩のホルマリン縮合物、アルキルベンゼンスルホ
ン酸ナトリウム塩、高級アルコールの硫酸エステルナト
リウム塩等の7ニオン性界面活性剤を使用した場合には
、界面活性剤の融点が高いため、芒硝、硫安等の水溶性
無機塩類を添加することにより容易に粉末化することが
できる。しかし、一般に水和剤用分散剤として用いられ
る非イオン性界面活性剤(例えば、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・ポリ
オキシプロピレン会ブロックポリマー等)、アニオン性
界面活性剤(例えば、ポリオキシエチレンアルキルアリ
ールエーテルの硫酸エステルアンモニウム塩、ポリオキ
シエチレンアルキルエーテルのリン酸エステル等)を粉
末化するためには、普通吸油能が大きい含水硅酸(Si
02・nH2O;普通くホワイトカーボン〉又はくシリ
カ〉と呼ばれれることが多い)が用いられている。
(従来の技術の問題点)
ところで、含水硅酸は吸油能に優れている反面、それ自
体水に溶解しないため、これに界面活性剤を吸着させた
粉末品を水中に投入したとき、水中へ溶出してくる界面
活性剤は精々30〜SOSに留まる。従って、水和剤用
分散剤として非イオン性界面活性剤、アニオン性界面活
性剤を使用する場合、充分な分散能を期待するためには
吸着量を見こんで必要量以上の活性剤を添加する必要を
生じ、これは価格アップの原因となるものであった。(Prior art) Pesticide hydrating agents are mainly composed of agricultural chemical active ingredients, clay minerals such as montmorillonite, and surfactants, and are easy to handle, and are suitable for agricultural chemical raw materials that cannot be emulsified due to the lack of suitable solvents. It is widely used today because it has the advantage that it can be used even in agricultural chemical ingredients that cannot be fluidized due to crystal precipitation over time. In the above, when a 7-ionic surfactant such as a formalin condensate of sodium naphthalene sulfonate, a sodium alkylbenzene sulfonate, or a sodium sulfate ester of a higher alcohol is used as a dispersant, the melting point of the surfactant is Since it is expensive, it can be easily powdered by adding water-soluble inorganic salts such as Glauber's salt and ammonium sulfate. However, nonionic surfactants (e.g., polyoxyethylene alkylaryl ether, polyoxyethylene/polyoxypropylene block polymers, etc.) and anionic surfactants (e.g., polyoxypropylene block polymers, etc.), which are generally used as dispersants for wettable powders, In order to powder sulfuric acid ester ammonium salts of oxyethylene alkylaryl ethers, phosphoric acid esters of polyoxyethylene alkyl ethers, etc.), hydrous silicic acid (Si), which has a large oil absorption capacity, is usually used.
02.nH2O; often referred to as white carbon or silica) is used. (Problems with conventional technology) By the way, although hydrated silicic acid has excellent oil-absorbing ability, it does not dissolve in water itself, so when a powdered product with a surfactant adsorbed to it is placed in water, it does not dissolve into the water. The surfactant eluted remains at 30 to SOS at most. Therefore, when using a nonionic surfactant or anionic surfactant as a dispersant for wettable powders, in order to expect sufficient dispersion ability, add more than the required amount of surfactant based on the amount of adsorption. This resulted in a need to increase the price.
本発明は、これまで農薬水和剤用担体として従−未使用
されたことのない澱粉加水分解物を選択することにより
、従来の含水硅酸の欠点を解消した新規な農薬水和剤用
分散剤組成物を提供するのを目的とする。The present invention provides a novel dispersion for agricultural chemical hydrating powders that eliminates the drawbacks of conventional hydrated silicic acid by selecting a starch hydrolyzate that has never been used as a carrier for agricultural chemical hydrating powders. The purpose of the present invention is to provide a drug composition.
(概要)
以上の目的を達成するため1本発明に係る農薬水和剤用
分散剤組成物は、界面活性剤が、噴霧乾燥又はドラム・
ドライヤー乾燥された顆粒状のV粉加水分解物、好まし
くは、デキストロース当量(DE)30以下の澱粉加水
分解物に吸着していることを特徴とする。
以下、発明を構成する諸要素について説明する。
(澱粉加水分解物)
本発明において用いる澱粉加水分解物は、ジャガイモ、
スィートコーン、小麦等から得る澱粉を通常の方法、例
えば酵素分解、酸分解で低分子量化した後、スプレード
ライヤー又はドラム・ドライヤー等を用いて乾燥させる
ことにより得られる。具体的な方法を述べると、例えば
、反応釜に水100部及び澱粉30部を加え、これに粉
末状のα−アミラーゼを加えて撹拌しながら50℃を保
ち。
目的とするDEの加水分解物が得られた時点で苛性ソー
ダを加えてα−アミラーゼを失活させ、酸で中和してス
ラリー状の醒粉加水分解液を得る0発明目的上、蕨粉加
水分解物のデキストロース当量(D E)は30以下で
あるのが望ましい。
次いで上の加水分解物のスラリーをスプレードライヤー
又はドラム・ドライヤーを用い、雰囲気温度的80℃〜
150℃で乾燥することにより、本発明の実施に適した
80メ5シx篩通30%以上の顆粒状澱粉加水分解物を
得る。
(界面活性剤)
本発明に用いる界面活性剤としては、例えばポリオキシ
エチレンアルキルエーテル、ポリオキシアルキルアリー
ルエーテル、ポリオキシエチレン・ポリオキシプロピレ
ン拳ブロックポリマー、ポリオキシアルキレン脂肪酸エ
ステルの如き非イオン性界面活性剤、ポリオキシアルキ
ルエーテルの硫酸塩、ポリオキシアルキルアリールエー
テルの硫酸塩、アルキル硫酸塩、ポリオキシアルキルエ
ーテルのリン酸エステル、ポリオキシアルキルアリール
エーテルのリン酸エステル、ジアルキルスルホコハク酸
エステル塩の如きアニオン性界面活性剤を挙げることが
できるが、勿論1例示のものに限られる訳ではない、な
お、これらの界面活性剤は、単独又は二種以上混合して
使用することができる。
(a薬木和剤用分散剤の調製法)
本発明の農薬水和剤用分散剤を調製するには、例えば、
顆粒状の澱粉加水分解物をリボンミキサー又はナウター
ミキサ−などに入れ、撹拌しながら界面活性剤を注入し
、均一に混合する。この際、必要に応じ、50〜80℃
に加熱してもよい。
(他の添加物)
本発明においては、更に必要に応じ、流動性向上剤とし
て、芒硝、硫安、塩安、ブドウ糖、尿素等を加えること
ができる。(Summary) In order to achieve the above objects, 1 the dispersant composition for agrochemical wettable powders according to the present invention is such that the surfactant is spray-dried or drum-dried.
It is characterized in that it is adsorbed onto a granular V powder hydrolyzate dried in a dryer, preferably a starch hydrolyzate having a dextrose equivalent (DE) of 30 or less. Below, various elements constituting the invention will be explained. (Starch hydrolyzate) The starch hydrolyzate used in the present invention includes potato,
It is obtained by reducing the molecular weight of starch obtained from sweet corn, wheat, etc. by a conventional method, such as enzymatic decomposition or acid decomposition, and then drying it using a spray dryer or drum dryer. To describe a specific method, for example, 100 parts of water and 30 parts of starch are added to a reaction vessel, and powdered α-amylase is added thereto, and the temperature is maintained at 50°C while stirring. When the desired DE hydrolyzate is obtained, caustic soda is added to inactivate α-amylase, and neutralized with acid to obtain a slurry-like fermented flour hydrolyzate. It is desirable that the dextrose equivalent (DE) of the decomposition product is 30 or less. Next, the slurry of the above hydrolyzate was heated to an ambient temperature of 80°C to 80°C using a spray dryer or drum dryer.
By drying at 150° C., a granular starch hydrolyzate having a sieve size of 30% or more is obtained, which is suitable for carrying out the present invention. (Surfactant) Examples of the surfactant used in the present invention include nonionic surfactants such as polyoxyethylene alkyl ether, polyoxyalkylaryl ether, polyoxyethylene/polyoxypropylene fist block polymer, and polyoxyalkylene fatty acid ester. Activators, such as polyoxyalkyl ether sulfates, polyoxyalkylaryl ether sulfates, alkyl sulfates, polyoxyalkyl ether phosphates, polyoxyalkylaryl ether phosphates, dialkyl sulfosuccinates, etc. Anionic surfactants can be mentioned, but of course the surfactants are not limited to one example. These surfactants can be used alone or in a mixture of two or more. (a) Method for preparing a dispersant for agrochemical powders of the present invention, for example,
The granular starch hydrolyzate is placed in a ribbon mixer or Nauta mixer, and the surfactant is injected while stirring to mix uniformly. At this time, if necessary, 50-80℃
May be heated to (Other additives) In the present invention, as required, fluidity improvers such as Glauber's salt, ammonium sulfate, ammonium chloride, glucose, and urea can be added.
本発明に用いる粗粒状の澱粉加水分解物は、比表面積が
大きく、界面活性剤を多量吸着して組成物(農薬水和剤
)の流動性を阻害しない、そして本発明組成物を含有す
る農薬水和剤を水に投入すると、V粉加水分解物自体水
に溶解してしまうので、該加水分解物に吸着された界面
活性剤は完全に水中に溶け、その効果を完全に発揮する
。加えて、溶解物は澱粉加水分解物に由来する適度の粘
度を有し、対象植物体に対する付着効果を有するため、
農薬の効果を最大限度発揮させることができる。The coarse starch hydrolyzate used in the present invention has a large specific surface area, adsorbs a large amount of surfactant and does not impede the fluidity of the composition (agrochemical hydrating agent), and the agrochemical containing the composition of the present invention. When the hydrating agent is added to water, the V-powder hydrolyzate itself dissolves in water, so the surfactant adsorbed to the hydrolyzate completely dissolves in water and fully exhibits its effect. In addition, the dissolved material has a moderate viscosity derived from starch hydrolyzate and has an adhesive effect on the target plant.
The effects of pesticides can be maximized.
以下、実験例び比較例を掲げ1本発明実施の態様及び効
果を詳説するが1本発明思想は、これらの例示により限
定されるものではない。
実験例〜1
水和剤用分散剤であるハイテノールNF−13(出願入
会社製のポリオキシエチレンアルキルアリールエーテル
の硫酸エステルアンモニウム塩の商標名)を用いて種々
のDEを有する澱粉加水分解物の吸着能を測定した。な
お、ここに云う「吸着能」は、澱粉加水分解物の流動性
がなくなるまでのハイテノールNF−13の吸着量を意
味する。
(以下余白)
表−1
実)1引≦
カープレックス#80(塩野義製薬鈎製の含水硅酸の商
標名)100部に、ハイテノールNF−13100部を
吸着させ、ハイテノールNF−13の水への溶解性を表
−1中の試料No、7と比較した。結果を下表−2に示
す。
〈測定方法〉
上記の試料5gを 100 mlビーカーに秤り取り、
水95gを加えスターラーで撹拌する。
測定時間ごとにガラスフィルター(3G−4)を使って
、その上澄液を吸引濾過する。グラスフィルターを 1
05℃で1時間乾燥し水不溶分を求める。
(以下余白)
表−2
下記に示すNAC(1−ナフチル−N−メチルカーバメ
ート)水利剤を調整し1表−1中の試料N007とカー
プレックス180100部にハイテノールNF−13t
oo部を吸着させた分散剤の比較試験を行なった。結果
を下表−3に示す。
1)配合処方
NAC原体 50
ジ−クライトC35
ラジオライト200 15−x
2)試料調製方法
ボールミルで2時間混合、80メワシ、全通。
3)試験方法
(1)水和性
農薬公定検査法による(5°硬水使用)。
(2)懸垂率
試料0.5gをビーカーに取り、少量の水で充分に分散
させ、250+sJlメスシリンダー(内径3.8cm
φ)に移し、5°硬水(水温20℃)で250 tsl
とし、上下に30回倒立する。30分静置後、上部22
5■文を抜き取り、残り251文をガラスフィルター(
3G−4)で濾過し、乾燥後。
下式により懸垂率を求める。
(以下余白)
表−3
上表−3の懸垂率の項から見て、従来分散剤を5z添加
しなければならないところが、本発明品では1〜2z添
加で充分であることが明らかである。Hereinafter, the embodiments and effects of the present invention will be explained in detail using experimental examples and comparative examples, but the idea of the present invention is not limited to these examples. Experimental Example ~ 1 Starch hydrolysates with various DEs using Hytenol NF-13 (trade name of sulfuric acid ester ammonium salt of polyoxyethylene alkylaryl ether manufactured by the applicant company), which is a dispersant for wettable powders. The adsorption capacity was measured. The term "adsorption capacity" as used herein means the amount of Hytenol NF-13 adsorbed until the starch hydrolyzate loses its fluidity. (Margin below) Table 1 Actual) 1 pull ≦ 100 parts of Carplex #80 (trade name of hydrated silicic acid manufactured by Shionogi & Co., Ltd.) was adsorbed with 100 parts of Hitenol NF-13. The solubility in water was compared with sample No. 7 in Table-1. The results are shown in Table 2 below. <Measurement method> Weigh 5g of the above sample into a 100ml beaker,
Add 95 g of water and stir with a stirrer. The supernatant liquid is suction filtered using a glass filter (3G-4) at each measurement time. 1 glass filter
Dry at 05°C for 1 hour and determine the water-insoluble content. (Leaving space below) Table 2 Prepare the NAC (1-naphthyl-N-methylcarbamate) irrigation agent shown below and add Hytenol NF-13t to sample N007 and Carplex 180,100 parts in Table 1.
A comparative test was conducted on a dispersant that adsorbed the oo portion. The results are shown in Table 3 below. 1) Blend formula NAC bulk 50 Zikrite C35 Radiolite 200 15-x 2) Sample preparation method Mix in a ball mill for 2 hours, 80 milliliter, all through. 3) Test method (1) Based on the official testing method for hydrating pesticides (using 5° hard water). (2) Take 0.5g of the suspension ratio sample in a beaker, thoroughly disperse it with a small amount of water, and use a 250+sJl graduated cylinder (inner diameter 3.8cm).
φ) and 250 tsl with 5° hard water (water temperature 20°C).
Then do a handstand up and down 30 times. After standing still for 30 minutes, the upper part 22
Extract 5 ■ sentences and pass the remaining 251 sentences through a glass filter (
After filtering with 3G-4) and drying. Find the suspension rate using the formula below. (The following is a blank space) Table 3 From the suspension ratio section in Table 3 above, it is clear that 5z of the dispersant had to be added in the conventional product, but it is sufficient to add 1 to 2z of the dispersant in the product of the present invention.
以上、説明した通り1本発明は、これまで農薬水和剤用
担体として従来使用されたことのない澱粉加水分解物を
選択することにより、従来の含水硅酸の欠点を解消した
新しい経済的な農薬水和剤用分散剤組成物を提供しえた
ことにより、農園芸及び関連産業に寄与しうる。
特許出願人 第一工業製薬株式会社As explained above, the present invention is a new economical product that eliminates the drawbacks of conventional hydrous silicic acid by selecting a starch hydrolyzate that has not been used as a carrier for agricultural chemical wettable powders. By providing a dispersant composition for agrochemical wettable powders, the present invention can contribute to agriculture, horticulture, and related industries. Patent applicant Daiichi Kogyo Seiyaku Co., Ltd.
Claims (6)
ていることを特徴とする農薬水和剤用分散剤組成物。(1) A dispersant composition for an agrochemical wettable powder, characterized in that a surfactant is adsorbed on a granular starch hydrolyzate.
DE)が、約30以下である特許請求の範囲第1項記載
の農薬水和剤用分散剤組成物。(2) Dextrose equivalent of granular starch hydrolyzate (
The dispersant composition for agrochemical wettable powders according to claim 1, wherein DE) is about 30 or less.
の顆粒子が30%以上含まれている特許請求の範囲第1
項又は第2項記載の農薬水和剤用分散剤組成物。(3) Claim 1 in which the granular starch hydrolyzate contains 30% or more of granules with a size of 80 mesh or more.
The dispersant composition for agrochemical hydration powders according to item 1 or 2.
0〜120重量部の界面活性剤を含む特許請求の範囲第
1項、第2項又は第3項記載の農薬水和剤用分散剤組成
物。(4) 5 parts per 100 parts by weight of granular starch hydrolyzate
The dispersant composition for an agrochemical wettable powder according to claim 1, 2 or 3, which contains 0 to 120 parts by weight of a surfactant.
霧乾燥したものである特許請求の範囲第1項から第4項
のいづれかに記載の農薬水和剤用分散剤組成物。(5) The dispersant composition for an agrochemical wettable powder according to any one of claims 1 to 4, wherein the granular starch hydrolyzate is obtained by spray-drying a starch hydrolyzate.
ラム・ドライヤー乾燥したものである特許請求の範囲第
1項から第4項のいづれかに記載の農薬水和剤用分散剤
組成物。(6) The dispersant composition for an agrochemical wettable powder according to any one of claims 1 to 4, wherein the granular starch hydrolyzate is obtained by drying a starch hydrolyzate using a drum dryer. .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62318177A JPH0714841B2 (en) | 1987-12-15 | 1987-12-15 | Dispersant composition for pesticide wettable powder |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62318177A JPH0714841B2 (en) | 1987-12-15 | 1987-12-15 | Dispersant composition for pesticide wettable powder |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01157903A true JPH01157903A (en) | 1989-06-21 |
| JPH0714841B2 JPH0714841B2 (en) | 1995-02-22 |
Family
ID=18096322
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62318177A Expired - Lifetime JPH0714841B2 (en) | 1987-12-15 | 1987-12-15 | Dispersant composition for pesticide wettable powder |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0714841B2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05132401A (en) * | 1991-02-12 | 1993-05-28 | Matsutani Kagaku Kogyo Kk | Agricultural chemical preparation and its production |
| JPH10139607A (en) * | 1996-11-08 | 1998-05-26 | Hokko Chem Ind Co Ltd | Pesticide granular wettable powder |
| JPH10218704A (en) * | 1997-02-13 | 1998-08-18 | Hokko Chem Ind Co Ltd | Improved pesticide granular wettable powder |
| WO2008061655A3 (en) * | 2006-11-24 | 2009-04-23 | Bayer Cropscience Ag | Plant protection granulates to be applied to the leaf surface |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57109702A (en) * | 1980-12-26 | 1982-07-08 | Kumiai Chem Ind Co Ltd | Powdered agricultural chemical emulsion |
| JPS6036402A (en) * | 1983-08-09 | 1985-02-25 | Nichiden Kagaku Kk | Composition of agricultural chemical |
-
1987
- 1987-12-15 JP JP62318177A patent/JPH0714841B2/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57109702A (en) * | 1980-12-26 | 1982-07-08 | Kumiai Chem Ind Co Ltd | Powdered agricultural chemical emulsion |
| JPS6036402A (en) * | 1983-08-09 | 1985-02-25 | Nichiden Kagaku Kk | Composition of agricultural chemical |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05132401A (en) * | 1991-02-12 | 1993-05-28 | Matsutani Kagaku Kogyo Kk | Agricultural chemical preparation and its production |
| JPH10139607A (en) * | 1996-11-08 | 1998-05-26 | Hokko Chem Ind Co Ltd | Pesticide granular wettable powder |
| JPH10218704A (en) * | 1997-02-13 | 1998-08-18 | Hokko Chem Ind Co Ltd | Improved pesticide granular wettable powder |
| WO2008061655A3 (en) * | 2006-11-24 | 2009-04-23 | Bayer Cropscience Ag | Plant protection granulates to be applied to the leaf surface |
| JP2010510261A (en) * | 2006-11-24 | 2010-04-02 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | Plant protective granule for application to leaf surface |
| US8323697B2 (en) | 2006-11-24 | 2012-12-04 | Bayer Intellectual Property Gmbh | Plant protection granulates to be applied to leaf surface |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0714841B2 (en) | 1995-02-22 |
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