JPS6334841B2 - - Google Patents
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- Publication number
- JPS6334841B2 JPS6334841B2 JP1734281A JP1734281A JPS6334841B2 JP S6334841 B2 JPS6334841 B2 JP S6334841B2 JP 1734281 A JP1734281 A JP 1734281A JP 1734281 A JP1734281 A JP 1734281A JP S6334841 B2 JPS6334841 B2 JP S6334841B2
- Authority
- JP
- Japan
- Prior art keywords
- powder
- present
- agrochemical
- fluidity
- less
- 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.)
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- 239000000843 powder Substances 0.000 claims description 46
- 239000003905 agrochemical Substances 0.000 claims description 34
- 239000000203 mixture Substances 0.000 claims description 26
- -1 ester compounds Chemical class 0.000 claims description 17
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 6
- 239000011707 mineral Substances 0.000 claims description 6
- 150000005846 sugar alcohols Polymers 0.000 claims description 6
- 125000002015 acyclic group Chemical group 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 239000000654 additive Substances 0.000 description 16
- 239000002994 raw material Substances 0.000 description 12
- 230000000996 additive effect Effects 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 239000000575 pesticide Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 239000000969 carrier Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 238000005188 flotation Methods 0.000 description 5
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000010419 fine particle Substances 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- QPPQHRDVPBTVEV-UHFFFAOYSA-N isopropyl dihydrogen phosphate Chemical compound CC(C)OP(O)(O)=O QPPQHRDVPBTVEV-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- IGURWOUVEYRFJD-UHFFFAOYSA-N (2,5-dimethoxy-3-methyl-4-nitrophenoxy)-dihydroxy-sulfanylidene-lambda5-phosphane Chemical compound CC1=C(C(=CC(=C1OC)OP(=S)(O)O)OC)[N+](=O)[O-] IGURWOUVEYRFJD-UHFFFAOYSA-N 0.000 description 1
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- OEOIWYCWCDBOPA-UHFFFAOYSA-N 6-methyl-heptanoic acid Chemical compound CC(C)CCCCC(O)=O OEOIWYCWCDBOPA-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 229940105990 diglycerin Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008202 granule composition Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
本発明は流動性が極めて良好で、かつ飛散浮遊
性の少ない農薬粉剤組成物に関する。
近年農薬散布時の環境汚染あるいは作業者に対
する安全性あるいは薬効などの観点から飛散浮遊
性の少ない農薬粉剤に対する要望が極めて高くな
つてきている。
一般に農薬粉剤は均一に散布されなければなら
ないが、そのためには流動性の良いことが必要で
ある。このため鉱物質微粉粒担体に農薬原体を吸
着させた粉剤に例えばイソプロピルホスフエート
の様な流動化を向上させる添加剤を添加すること
によつて得られる流動性が改善された粉剤組成物
は散布時の分散性、吐粉性は改善されるが飛散浮
遊性の増加を招くのが常であり流動性、吐粉性を
上げながら同時に飛散浮遊性を低下させることは
非常に困難な問題であつた。
しかし前記した様な安全性の観点からこの問題
の解決を求める声は極めて高く業界でもその要望
に応えるべく盛んに検討が行なわれている。
例えば流動パラフイン,ポリアルキレングリコ
ール,リン酸エステル系アニオン界面活性剤,30
℃で液状を呈するソルビタンエステル系化合物、
イソプロピルホスフエートと、一定粘度以上の不
揮発性液状物との混合物等を添加剤として使用す
る提案又は一定値以上の粘度を有する疎水性有機
化合物と一定値以上の粘度を有する担体とを併用
する提案等が従来から行なわれている。
しかしながらこれらの方法は粉剤組成物の飛散
浮遊性防止性及び流動性向上の双方を狙いとして
いるものの、添加剤として全て油状物質を使用す
ることによつてそれらの油状物質の有する粘結作
用を利用するものであるためややもすれば粉剤を
べとつかせたり流動性を低下させたりする危険性
を含んでいる。従つて上記添加剤を使用した粉剤
組成物はべとつきや流動性を改善するために、そ
れらの改善に効果を有するホワイトカーボンの如
き吸油能の高い補助担体を添加剤と併用している
ものが多い。
更に現在では農薬使用時の安全性に特に力点を
おくために粉剤の飛散浮遊性を下げることを重視
しそのため微細粒子の含量を一定量以下に抑えた
所謂分級担体を使用することが盛んになつてい
る。しかしこの場合は粉剤の飛散浮遊性は低下す
る反面粉剤がべとついたり流動性が低下する傾向
が生じ易い。
殊に液状の農薬原体と分級担体を使用した粉剤
の場合はその傾向が著るしくなるためにホワイト
カーボンと添加剤との使用量が増加するのが普通
であるがそれにも拘らず粉剤の飛散浮遊防止性と
流動性との両方を同時に満足させることは難かし
く又経済的にも高くついているのが現状である。
上記の様な状況に鑑み本発明者等は農薬原体の
性状に拘らずできる丈添加剤の使用を少なくしな
がら飛散浮遊防止性及び流動性の高い農薬粉剤を
得ることを目的として鋭意研究した結果特定の化
学構造を有するエステル化合物を添加剤として、
5ミクロン以下の微粒子含量が10重量%以下であ
る分級担体を使用する農薬粉剤に使用すれば上記
目的が達成されることを見出して本発明を完成さ
せるに至つた。
即ち本発明の要旨は水酸基を3個以上有する総
炭素数12以下の非環状多価アルコールと、総炭素
数8〜22を有し直鎖又は分岐で飽和又は不飽和の
一価カルボン酸とを反応させて得られる分子中に
少くとも一個の水酸基を有する部分エステル化合
物の群から選ばれる単独品又は二種以上の混合物
を0.2〜3重量%含有し、かつ粒径が5ミクロン
以下の微粒子の含量が10重量%以下である農薬粉
剤用鉱物質担体を用いることを特徴としてなる農
薬粉剤組成物に関するものである。
本発明における部分エステル化合物の原料とし
て使用する水酸基を3個以上有する総炭素数12以
下の非環状多価アルコールの具体例としてはペン
タエリスリトール,ジペンタエリスリトール,ト
リメチロールプロパン,グリセリン,ジグリセリ
ン等が挙げられる。尚本発明では使用する多価ア
ルコールが非環状アルコールであることを特定し
ているが上記した如き非環状多価アルコールを使
用した本発明における部分エステル化合物は環状
多価アルコールエステル、例えば高級脂肪酸ソル
ビタンエステル及びそのエチレンオキシド付加物
等に比較してより優れた性能を有しており特に粉
剤組成物の流動性を向上させる。
又本発明における部分エステル化合物の原料と
して使用する総炭素数8〜22を有し直鎖又は分岐
で飽和又は不飽和の一価カルボン酸の具体例とし
てはn―オクチル酸,iso―オクチル酸,ラウリ
ン酸,パルミチン酸,オレイン酸,n―ステアリ
ン酸,iso―ステアリン酸,ヤシ油脂肪酸,牛脂
脂肪酸,米ヌカ脂肪酸等が挙げられる。
上記原料アルコールと原料カルボン酸とを反応
させて得られる本発明における化合物としては上
記の特定された化学構造を有するものであればい
ずれも使用できるが、特に水酸基が全てエステル
結合した完全エステルよりも水酸基が少くとも一
個残された部分エステルを使用するのが効果の点
で好ましいのである。
本発明における部分エステル化合物の具体例と
してはジ―n―ステアリン酸ペンタエリスリトー
ルエステル,モノ―オレイン酸ペンタエリスリト
ールエステル,ジ―ラウリン酸ペンタエリスリト
ールエステル,ジ―n―ステアリン酸ジペンタエ
リスリトールエステル,モノ―n―ステアリン酸
トリメチロールプロパンエステル,ジ―牛脂脂肪
酸トリメチロールプロパンエステル,iso―オク
チル―n―ステアリン酸トリメチロールプロパン
エステル,ジ―n―ステアリン酸グリセリンエス
テル,トリ―n―ステアリン酸トリメチロールプ
ロパンエステル等が挙げられる。
本発明における部分エステル化合物は前記原料
アルコールと原料カルボン酸とを使用して常法に
従い酸性あるいは塩基性触媒の存在下脱水エステ
ル化することによつて容易に得ることができる。
本発明における部分エステル化合物の添加剤と
しての使用量は農薬原体の性状・作用性に拘らず
農薬粉剤に対して0.2〜3重量%であり好ましく
は0.5〜2重量%である。添加量が0.2重量%より
少ないと十分な飛散浮遊防止性、流動性が得られ
ず、3重量%より多くても添加量に見合う効果が
得られない。
又農薬原体の性状,作用性に合せて本発明にお
ける部分エステル化合物の添加剤を選択すれば上
記添加量でホワイトカーボンを添加することなく
性能の良い粉剤組成物を得ることができるが、勿
論ホワイトカーボンの如き補助担体併用も可能で
ある。
次に本発明で使用する農薬粉剤用鉱物質担体と
してはクレー,タルク,カオリン,珪藻土等の5
ミクロン以下の微粒子の含量が10重量%以下であ
る粉末が挙げられる。
又本発明では従来からの添加剤である油脂類,
グリコール類,非イオン界面活性剤,ホスフエー
ト系アニオン界面活性剤や農薬原体安定剤として
使用されるホスフエート化合物などを本発明の効
果を損わない範囲で併用することができる。
本発明の農薬粉剤組成物は農薬原体,部分エス
テル化合物,鉱物質担体更に必要ならば補助担体
を通常の農薬粉剤組成物の製造法によつて均一に
混合すれば容易に得ることができるが必要であれ
ばプレミツクス法によつても製造することができ
る。
本発明の農薬粉剤組成物において部分エステル
化合物が添加剤として優れた性能を発揮する作用
機構については良く判らないが、特定の化学構造
を有するために従来の油状添加剤の粘結作用と異
なつて潤滑性、粘結性等の各性質が総合して効果
的に粉剤に働く結果粉剤の飛散浮遊防止性と流動
性と云う一面では相反する性質を共に向上させる
ものと思われる。
以下実施例によつて本発明の農薬粉剤組成物及
びその効果を説明するが本発明はこれらだけに限
定されるものではない。
実施例 1
担体として5ミクロン以下の微粒子含量を10重
量%にした農薬粉剤用クレー(以下カツトクレー
と云う)97g、添加剤としてジn―ステアリン酸
トリメチロールプロパンエステル1g、農薬原体
として常温で固状の1―ナフチル―N―メチルカ
ーバメート(以下NACと云う)2gを小型粉砕
器に入れて90秒程撹拌粉砕し均一な本発明の農薬
粉剤組成物を得る。
実施例 10
担体としてカツトクレー96g、添加剤としてジ
―n―ステアリン酸トリメチロールプロパンエス
テル1g、農薬原体として常温で液状のO,O―
ジメチル―O―(3―メチル―4―ニトロフエニ
ル)ホスホロチオエート(以下MEPと云う)2
g、補助担体としてホワイトカーボン1gを小型
粉砕器に入れて90秒程撹拌粉砕し均一な本発明の
農薬粉剤組成物を得る。
実施例2〜9,11〜17及び比較例3,4,5,
8,9,10
表―1に記載した担体、添加剤、農薬原体又は
それらに補助担体を加えて実施例1又は10と同様
に撹拌粉砕して均一な本発明又は比較例の農薬粉
剤組成物を得る。
比較例1及び6
表―1に記載した担体及び農薬原体を小型粉砕
器に入れて90秒程撹拌粉砕した。比較例1では均
一な粒剤組成物が得られたが、比較例6では得ら
れた粉剤のべとつきが大きく製品にできなかつ
た。
比較例2及び7
表―1に記載した担体,農薬原体及び補助担体
を小型粉砕器に入れて90秒程撹拌し均一な農薬粉
剤組成物を得る。
得られた本発明及び比較例の農薬粉剤組成物に
ついて散布時の飛散浮遊性と流動性とを下記の方
法で測定した。
飛散浮遊性
粉剤の標準吐粉試験機を用いて10gの農薬粉剤
組成物を1米立方の箱内に下向きに散布し5分間
放置した後散布管の上部40cmの位置に飛散浮遊す
る粒子を水75mlを入れた吸収管に30/分の流速
で1分間吸収させた。この懸濁液にドデシルベン
ゼンスルホン酸ソーダの6%水溶液1mlを加えて
ドデシルベンゼンスルホン酸ソーダの0.08%水溶
液を対照として層長1cm,波長610mμにおける
透過率を測定した。下記態様の浮遊性・指数を以
て飛散浮遊性を表わした。浮遊性指数が大きい程
飛散浮遊性が高い。
流動性
16メツシユ篩(直径62mm,高さ33mm)に農薬粉
剤組成物50gを入れ篩をバイブレーターで振動さ
せ上皿天秤に落下させる。
落下する粉剤が10〜30gに達する迄の落下時間
(秒)を以て流動性を表わした。
落下時間が短い程流動性が大きい。
測定した結果は次の表―1に示す如くであつ
た。
The present invention relates to an agrochemical powder composition that has extremely good fluidity and less scattering and flotation. In recent years, there has been an extremely high demand for agrochemical powders with low scattering and floating properties from the viewpoint of environmental pollution during agrochemical spraying, safety for workers, and medicinal efficacy. Generally, agrochemical powders must be uniformly dispersed, and for this purpose they need to have good fluidity. For this reason, a powder composition with improved fluidity can be obtained by adding an additive that improves fluidity, such as isopropyl phosphate, to a powder in which a pesticide active ingredient is adsorbed onto a mineral fine particle carrier. Although dispersibility and powder dispersion during spraying are improved, this usually results in an increase in scattering and flotation, and it is a very difficult problem to simultaneously improve fluidity and powder dispersion and reduce scattering and flotation. It was hot. However, from the viewpoint of safety as described above, there is a strong demand for a solution to this problem, and the industry is actively conducting studies to meet this demand. For example, liquid paraffin, polyalkylene glycol, phosphate ester anionic surfactant, 30
A sorbitan ester compound that is liquid at °C.
A proposal to use a mixture of isopropyl phosphate and a non-volatile liquid substance with a viscosity above a certain value as an additive, or a proposal to use a combination of a hydrophobic organic compound with a viscosity above a certain value and a carrier with a viscosity above a certain value etc. have been conventionally practiced. However, although these methods aim to both prevent scattering and improve fluidity of powder compositions, they do not utilize the caking effect of these oily substances by using all oily substances as additives. Therefore, there is a risk of making the powder sticky or reducing its fluidity. Therefore, in order to improve stickiness and fluidity, powder compositions using the above additives often use an auxiliary carrier with a high oil absorption capacity, such as white carbon, in combination with the additive, which is effective in improving these properties. . Furthermore, in order to place special emphasis on safety when using agricultural chemicals, it is now important to reduce the scattering and buoyancy of powder agents, and for this reason, the use of so-called classified carriers that suppress the content of fine particles below a certain amount has become popular. ing. However, in this case, while the scattering and flotation properties of the powder are reduced, the powder tends to become sticky and its fluidity tends to be reduced. This tendency is particularly pronounced in the case of powders that use liquid agricultural chemical ingredients and classified carriers, so the amount of white carbon and additives used increases. At present, it is difficult to simultaneously satisfy both anti-scattering properties and fluidity, and it is also economically expensive. In view of the above situation, the present inventors conducted intensive research with the aim of obtaining a pesticide powder with high scattering and floating resistance and high fluidity while reducing the use of additives that can be used regardless of the properties of the pesticide raw material. As a result, using an ester compound with a specific chemical structure as an additive,
The present invention has been completed based on the discovery that the above object can be achieved by using a classified carrier with a particle content of 5 microns or less of 10% by weight or less in an agrochemical powder. That is, the gist of the present invention is that an acyclic polyhydric alcohol having 3 or more hydroxyl groups and a total carbon number of 12 or less, and a linear or branched, saturated or unsaturated monohydric carboxylic acid having a total carbon number of 8 to 22. Fine particles containing 0.2 to 3% by weight of a single product or a mixture of two or more selected from the group of partial ester compounds having at least one hydroxyl group in the molecule obtained by reaction, and having a particle size of 5 microns or less. The present invention relates to an agrochemical powder composition characterized by using a mineral carrier for agrochemical powder having a content of 10% by weight or less. Specific examples of acyclic polyhydric alcohols having 3 or more hydroxyl groups and a total of 12 or less carbon atoms to be used as a raw material for the partial ester compound in the present invention include pentaerythritol, dipentaerythritol, trimethylolpropane, glycerin, diglycerin, etc. Can be mentioned. Although the present invention specifies that the polyhydric alcohol used is an acyclic alcohol, the partial ester compound in the present invention using the above-mentioned acyclic polyhydric alcohol is a cyclic polyhydric alcohol ester, such as higher fatty acid sorbitan. It has superior performance compared to esters and their ethylene oxide adducts, and particularly improves the fluidity of powder compositions. Further, specific examples of linear or branched, saturated or unsaturated monohydric carboxylic acids having a total carbon number of 8 to 22 used as raw materials for the partial ester compound in the present invention include n-octylic acid, iso-octylic acid, Examples include lauric acid, palmitic acid, oleic acid, n-stearic acid, iso-stearic acid, coconut oil fatty acid, beef tallow fatty acid, and rice bran fatty acid. As the compound in the present invention obtained by reacting the raw material alcohol and the raw material carboxylic acid, any compound having the chemical structure specified above can be used, but in particular, complete esters in which all hydroxyl groups are ester-bonded can be used. From the viewpoint of effectiveness, it is preferable to use a partial ester in which at least one hydroxyl group remains. Specific examples of the partial ester compound in the present invention include di-n-stearate pentaerythritol ester, mono-oleate pentaerythritol ester, di-laurate pentaerythritol ester, di-n-stearate dipentaerythritol ester, mono- n-stearate trimethylolpropane ester, di-tallow fatty acid trimethylolpropane ester, iso-octyl-n-stearate trimethylolpropane ester, di-n-stearate glycerin ester, tri-n-stearate trimethylolpropane ester etc. The partial ester compound in the present invention can be easily obtained by dehydrating and esterifying the raw material alcohol and the raw material carboxylic acid in the presence of an acidic or basic catalyst according to a conventional method. The amount of the partial ester compound used as an additive in the present invention is 0.2 to 3% by weight, preferably 0.5 to 2% by weight, based on the agricultural chemical powder, regardless of the properties and effects of the agricultural chemical raw material. If the amount added is less than 0.2% by weight, sufficient anti-scattering properties and fluidity will not be obtained, and if it is more than 3% by weight, the effect commensurate with the amount added will not be obtained. Moreover, if the additive of the partial ester compound in the present invention is selected according to the properties and action of the agricultural chemical raw material, it is possible to obtain a powder composition with good performance without adding white carbon at the above-mentioned addition amount. It is also possible to use an auxiliary carrier such as white carbon. Next, mineral carriers for agricultural chemical powders used in the present invention include clay, talc, kaolin, diatomaceous earth, etc.
Examples include powders in which the content of submicron particles is 10% by weight or less. In addition, in the present invention, conventional additives such as oils and fats,
Glycols, nonionic surfactants, phosphate anionic surfactants, phosphate compounds used as agricultural chemical stabilizers, and the like can be used in combination without impairing the effects of the present invention. The agrochemical powder composition of the present invention can be easily obtained by uniformly mixing the agrochemical raw material, a partial ester compound, a mineral carrier, and, if necessary, an auxiliary carrier by a conventional method for producing agrochemical powder compositions. If necessary, it can also be manufactured by a premix method. The mechanism of action by which the partial ester compound exhibits excellent performance as an additive in the agrochemical powder composition of the present invention is not well understood, but because it has a specific chemical structure, it has a caking effect that is different from that of conventional oil additives. It is thought that the properties such as lubricity and caking properties work together effectively on the powder, thereby improving both the anti-scattering and fluidity of the powder, which are contradictory properties. The agrochemical powder composition of the present invention and its effects will be explained below with reference to Examples, but the present invention is not limited thereto. Example 1 97 g of clay for agricultural chemical powders (hereinafter referred to as "Katsuto Clay") containing 10% by weight of fine particles of 5 microns or less as a carrier, 1 g of di-n-stearate trimethylolpropane ester as an additive, and 1 g of di-n-stearate trimethylolpropane ester as an agricultural chemical raw material that is solid at room temperature. 2 g of 1-naphthyl-N-methyl carbamate (hereinafter referred to as NAC) was placed in a small pulverizer and pulverized with stirring for about 90 seconds to obtain a uniform agrochemical powder composition of the present invention. Example 10 96 g of cut clay as a carrier, 1 g of di-n-stearic acid trimethylolpropane ester as an additive, and O, O-, which is liquid at room temperature as an agricultural chemical ingredient.
Dimethyl-O-(3-methyl-4-nitrophenyl) phosphorothioate (hereinafter referred to as MEP) 2
g. 1 g of white carbon as an auxiliary carrier is placed in a small pulverizer and pulverized with stirring for about 90 seconds to obtain a uniform agrochemical powder composition of the present invention. Examples 2 to 9, 11 to 17 and comparative examples 3, 4, 5,
8,9,10 The carriers, additives, agricultural chemical ingredients listed in Table 1, or auxiliary carriers are added thereto and stirred and ground in the same manner as in Example 1 or 10 to obtain a uniform agricultural chemical powder composition of the present invention or comparative example. get something Comparative Examples 1 and 6 The carriers and agricultural chemical ingredients listed in Table 1 were placed in a small pulverizer and agitated and pulverized for about 90 seconds. In Comparative Example 1, a uniform granule composition was obtained, but in Comparative Example 6, the powder obtained was so sticky that it could not be made into a product. Comparative Examples 2 and 7 The carrier, agricultural chemical raw material, and auxiliary carrier listed in Table 1 were placed in a small pulverizer and stirred for about 90 seconds to obtain a uniform agricultural chemical powder composition. The resulting agrochemical powder compositions of the present invention and comparative examples were measured for scattering buoyancy and fluidity during spraying using the following methods. Dispersion and Floatability Using a standard dust powder tester, spray 10g of the pesticide powder composition downward into a 1 m3 box, leave it for 5 minutes, and then remove the suspended particles at a position 40cm above the spray tube with water. Absorption was carried out for 1 minute at a flow rate of 30/min into an absorption tube containing 75 ml. To this suspension, 1 ml of a 6% aqueous solution of sodium dodecylbenzenesulfonate was added, and the transmittance at a layer length of 1 cm and a wavelength of 610 mμ was measured using a 0.08% aqueous solution of sodium dodecylbenzenesulfonate as a control. The scattering buoyancy was expressed using the buoyancy index shown below. The larger the buoyancy index is, the higher the buoyancy is. Fluidity: Put 50 g of the pesticide powder composition into a 16-mesh sieve (diameter 62 mm, height 33 mm), vibrate the sieve with a vibrator, and let it fall onto a top balance. Fluidity was expressed as the falling time (in seconds) until the powder reached 10 to 30 g. The shorter the falling time, the greater the fluidity. The measured results were as shown in Table 1 below.
【表】【table】
【表】
農薬粉剤組成の欄の数字は各成分の農薬粉剤組成
物中における重量%を表わす。
○* 粉剤組成物のべとつきのため測定不能。
表―1に示した結果から本発明の農薬粉剤組成
物は比較例に比較して農薬原体の性状に拘らず飛
散浮遊性が著るしく低くかつ同時に流動性が極め
て良好であることが明らかである。[Table] The numbers in the column of pesticide powder composition represent the weight percent of each component in the pesticide powder composition.
○* Unable to measure due to stickiness of powder composition.
From the results shown in Table 1, it is clear that the agrochemical powder composition of the present invention has significantly lower scattering and flotation properties than the comparative examples, regardless of the properties of the agrochemical substance, and at the same time has extremely good fluidity. It is.
Claims (1)
環状多価アルコールと、総炭素数8〜22を有し直
鎖又は分岐で飽和又は不飽和の一価カルボン酸と
を反応させて得られる分子中に少くとも一個の水
酸基を有する部分エステル化合物の群から選ばれ
る単独品又は二種以上の混合物を0.2〜3重量%
含有し、かつ粉径が5ミクロン以下の微粒子の含
量が10重量%以下である農薬粉剤用鉱物質担体を
用いることを特徴としてなる農薬粉剤組成物。1 Obtained by reacting an acyclic polyhydric alcohol having 3 or more hydroxyl groups and a total of 12 or less carbon atoms with a linear or branched, saturated or unsaturated monohydric carboxylic acid having a total of 8 to 22 carbon atoms. 0.2 to 3% by weight of a single product or a mixture of two or more selected from the group of partial ester compounds having at least one hydroxyl group in the molecule.
1. An agrochemical powder composition characterized by using a mineral carrier for an agrochemical powder, which contains a mineral carrier having a particle size of 5 microns or less in a content of 10% by weight or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1734281A JPS57130902A (en) | 1981-02-07 | 1981-02-07 | Dust composition for agricultural purpose |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1734281A JPS57130902A (en) | 1981-02-07 | 1981-02-07 | Dust composition for agricultural purpose |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57130902A JPS57130902A (en) | 1982-08-13 |
JPS6334841B2 true JPS6334841B2 (en) | 1988-07-12 |
Family
ID=11941376
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1734281A Granted JPS57130902A (en) | 1981-02-07 | 1981-02-07 | Dust composition for agricultural purpose |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57130902A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NO300383B1 (en) * | 1991-09-06 | 1997-05-20 | Colgate Palmolive Co | softergent |
DE102004017222A1 (en) * | 2004-04-05 | 2005-10-20 | Cognis Ip Man Gmbh | Sensory waxes for cosmetic and / or pharmaceutical formulations |
-
1981
- 1981-02-07 JP JP1734281A patent/JPS57130902A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS57130902A (en) | 1982-08-13 |
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