JPS6299356A - Granular wettable powder composition - Google Patents

Granular wettable powder composition

Info

Publication number
JPS6299356A
JPS6299356A JP23911585A JP23911585A JPS6299356A JP S6299356 A JPS6299356 A JP S6299356A JP 23911585 A JP23911585 A JP 23911585A JP 23911585 A JP23911585 A JP 23911585A JP S6299356 A JPS6299356 A JP S6299356A
Authority
JP
Japan
Prior art keywords
parts
formula
diphenyl ether
disulfonic acid
wettable powder
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
JP23911585A
Other languages
Japanese (ja)
Inventor
Tetsuo Ishii
哲雄 石井
Yoshihiro Nonaka
義弘 野中
Katsuji Sasaki
勝司 佐々木
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.)
Nippon Nyukazai Co Ltd
Original Assignee
Nippon Nyukazai 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 Nippon Nyukazai Co Ltd filed Critical Nippon Nyukazai Co Ltd
Priority to JP23911585A priority Critical patent/JPS6299356A/en
Publication of JPS6299356A publication Critical patent/JPS6299356A/en
Pending legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To provide the titled composition having improved disintegrability and dispersibility of granular agricultural chemical, by adding an alkyl diphenyl ether disulfonic acid derivative to an active agricultural chemical component. CONSTITUTION:An alkyl diphenyl ether disulfonic acid derivative of formula (R is 6-16C alkyl; M is alkali metal atom, alkaline earth metal corresponding to univalent, ammonium, etc.) is used as a component of the objective composition. Application of an agricultural chemical in the form of wettable powder is widely used as an extremely effective method among application processes of agricultural chemicals. It has been found that the compound of formula is effective to impart granular agricultural chemicals with extremely excellent disintegrability and dispersibility in water as a dispersant giving stable suspending property comparable to powdery wettable powder. The compound of formula can be easily produced by sulfonating an alkyl diphenyl ether by conventional method and neutralizing the product. The amount of the compound added to the composition is usually 2-20wt%.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は農薬組成物に関し、更に詳しくは顆粒状農薬の
水相剤において、優れ次崩壊注と分散性全厚える分散剤
を含有し斥組放物に関する。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to an agrochemical composition, and more particularly, to an aqueous phase agent for granular agrochemicals containing a dispersant having excellent disintegration and dispersibility throughout the entire thickness. Concerning parabola.

〔従来の技術〕[Conventional technology]

農薬撒布の一方法として、農薬有効成分を水相剤として
撒布する方法に、極めて有効なものとして広く一般に使
用されている。そして比較的最近までは農薬有効取分の
分散性をよくするために、微粉化され7を農薬を便用し
た粉状水相剤が使用されていた。しかしながら近年農薬
撒布の安全性が1視されてきておシ、粉状水相剤につい
ても分散液製造時の激しい粉立ちによる安全衛生面が問
題とされるに至り、顆粒状水相剤が開発されて来た。そ
れと同時に顆粒状水相剤の分散性をよくするために種々
の方法が検討されている。例えは、水浴性無機塩を配合
する方法(%公開53−12577号)、糖類、ナフタ
レンスルホン酸系界面活性剤およびリン酸アルカリ金属
塩を配合する方法(特開昭57−163303号)、サ
ルフェート系アニオン界面活性剤と非イオン界面活性剤
とを組合せて配合する方法(t¥f開昭59−1938
03号)などがあげられる。
As a method of spraying pesticides, it is widely and generally used as an extremely effective method for spraying pesticide active ingredients in the form of an aqueous phase agent. Until relatively recently, in order to improve the dispersibility of the effective fraction of pesticides, powdered aqueous phase agents containing micronized pesticides have been used. However, in recent years, the safety of spraying pesticides has become a top priority, and the safety and health aspects of powdered aqueous agents due to the heavy dusting during dispersion production have become a problem, and granular aqueous agents have been developed. I've been At the same time, various methods are being studied to improve the dispersibility of granular aqueous phase agents. For example, a method of blending a water-bathable inorganic salt (% Publication No. 53-12577), a method of blending a sugar, a naphthalene sulfonic acid surfactant, and an alkali metal phosphate salt (JP-A-57-163303), A method of combining and blending an anionic surfactant and a nonionic surfactant (t¥f Kaisho 59-1938
No. 03).

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

前記のように水相剤の安全性を得るための顆粒状水和剤
組成物についても、いくつかの分散剤の添加の研究がな
されているが、これらはいずれも、崩壊性や一時的水中
分散註については改良され優れた点を有してはいるもの
の、低希釈倍率および高希釈倍率における懸垂性につい
ては粉状水相剤に比べて著しく劣る次め、長時間安定し
た均一な懸濁性が得られず、その結果。
As mentioned above, research has been conducted on the addition of several dispersants to granular wettable powder compositions to ensure the safety of aqueous phase agents. Although it has improved and excellent dispersion properties, its suspension properties at low and high dilution ratios are significantly inferior to powdered aqueous phase agents, and it is difficult to obtain stable and uniform suspension for a long time. As a result of not being able to have sex.

散布時の丹分散、再撹拌等りで必要でおシ、問題とされ
、粉状水相剤の場合と同様な安定した懸濁性を得るため
の分散剤の開発が安来されていた。
Due to the necessity and problem of redundant dispersion and re-stirring during spraying, efforts were made to develop a dispersant to obtain stable suspension properties similar to those of powdered aqueous phase agents.

〔問題点を解決する穴めの手段〕[Measures to solve problems]

本発明者らは、前記の問題点を解決して粒状であシなが
ら粉状水相剤と同等の安定した懸濁性全厚える分散剤を
得るために、各種化合物特に界面活性剤について鋭意研
究金型ねた結果。
In order to solve the above-mentioned problems and obtain a granular dispersant with stable suspending properties equivalent to powdery aqueous phase agents, the present inventors have worked diligently on various compounds, especially surfactants. Research mold results.

後記一般式(I)で示されるアルキルジフェニルエーテ
ルジスルホン酸誘導体が顆粒状農薬に極めて優れた崩壊
性と水分散性を与えることを見出して本発明を光取した
口 即ち1本発明の顆粒伏水相剤組成物に、分散剤として、
一般式 %式% (式中、Rは炭素数6〜1S個のアルキル基を示し、M
はアルカリ金属原子、1価相当のアルカリ土類金kI4
原子、アンモニウム基、またはアルキル若しくはヒドロ
キシアルキル置換アンモニウム基を示す。〕を有するア
ルキルジフェニルエーテルジスルホン酸酵導体全含有す
ることを特徴とするものである。
The present invention was achieved by discovering that the alkyl diphenyl ether disulfonic acid derivative represented by the general formula (I) below provides extremely excellent disintegration properties and water dispersibility to granular agricultural chemicals. In the agent composition, as a dispersant,
General formula%Formula% (wherein, R represents an alkyl group having 6 to 1S carbon atoms, M
is an alkali metal atom, monovalent equivalent alkaline earth gold kI4
Represents an atom, an ammonium group, or an alkyl- or hydroxyalkyl-substituted ammonium group. It is characterized by containing all of the alkyl diphenyl ether disulfonic acid enzyme derivatives having the following properties.

前記式(I)で表わされる代表的な化合物としては、次
のようなものが例示される。
The following are exemplified as typical compounds represented by the above formula (I).

1)  ドデシルジフェニルエーテルジスルホン酸ジナ
トリウム塩 2)  ドデシルジフェニルエーテルジスルホン酸ジ(
1/2)カルシウム塩 3)オクチルジフェニルエーテルジスルホン酸ジアンモ
ニウム塩 リ ドデシルジフエ二ルエーテルジスルホン敏ビストリ
エタノールアミン塩 5)ヘキサデシルジフェニルエーテルジスルスルホン酸
ジナトリウム塩 6)オクチルジフェニルエーテルジスルホン酸ビストリ
メチルアミン塩 前記式(I)で示される化合物は、アルキルジフェニル
エーテル?:g@によってスルホン化シ。
1) Dodecyl diphenyl ether disulfonic acid disodium salt 2) Dodecyl diphenyl ether disulfonic acid disodium salt (
1/2) Calcium salt 3) Octyl diphenyl ether disulfonic acid diammonium salt Dodecyl diphenyl ether disulfonic acid bistriethanolamine salt 5) Hexadecyl diphenyl ether disulfonic acid disodium salt 6) Octyl diphenyl ether disulfonic acid bis trimethylamine salt Formula (I) ) Is the compound represented by alkyldiphenyl ether? : Sulfonated by g@.

中和することによって容易に製造される。ジスルホン化
によ92個のスルホン基は、2個のフェニル基に夫々1
個づつ導入されるが、スルホン基の位置は特定の位置に
入らず混合物が得られる。クロマトグラフィー等の暦法
によって分離することは可能であるが、コスト高となυ
、単離することによる効果も特に混合物と変らないので
、通常混合物のま又使用される。
Easily produced by neutralization. By disulfonation, 92 sulfone groups are converted to 1 to 2 phenyl groups, respectively.
Although the sulfone groups are introduced one by one, a mixture is obtained without placing the sulfone group in a specific position. It is possible to separate by calorimetric methods such as chromatography, but it is expensive and
Since the effect of isolation is not particularly different from that of a mixture, it is usually used as a mixture.

本発明に係る水和剤用の粗粒組成物は、電性によって製
造される。例えは農薬有効成分に式(I)で示される化
合物を加え、また必要に応じて通常顆粒形成に使用され
る担体例えば無筋性含水珪酸ナトリウム、ケイソウ上床
、クレー類、ホワイトカーボンなどを使用して、押出造
粒、噴霧造粒、転勤造粒、破砕造粒などの暦法によって
製造される。
The coarse particle composition for wettable powders according to the present invention is produced by electroconversion. For example, the compound represented by the formula (I) is added to the active ingredient of the agricultural chemical, and if necessary, carriers commonly used for granule formation, such as unreinforced hydrous sodium silicate, diatomaceous supernatant, clays, white carbon, etc., are used. It is manufactured by methods such as extrusion granulation, spray granulation, transfer granulation, and crushing granulation.

農薬有効成分としては、従米水相剤として使用されてい
るものに特に限定なく適用することができる。例えは、
殺虫沖」としてはMPMC。
As the agricultural chemical active ingredient, those used as an aqueous phase agent can be used without particular limitation. For example,
MPMC as “Insecticide Offshore”.

XMC、BPMC、MEP 、 MPP 、72ソン、
 PHC。
XMC, BPMC, MEP, MPP, 72son,
PHC.

BRP 、 MTMC、NAC、DDVP 、ダイアジ
ノン。
BRP, MTMC, NAC, DDVP, diazinon.

PAP 、 DEP 、 PMP 、ホルモチオン、チ
オメトン。
PAP, DEP, PMP, formothion, thiometone.

エチルチオメトン、フェニンブロモV −ト、 ジメチ
ルビンホス、ピリダフェンチオン、アセフェート、クロ
ルベンジレート、ピリミホスメチル、ビナバクリル、ジ
メトエート、 ESP 、 BPPS 。
Ethylthiometone, pheninebromo V-to, dimethylvinphos, pyridafenthion, acephate, chlorbenzilate, pirimiphos methyl, binabacryl, dimethoate, ESP, BPPS.

プロパホスjMIPC、ボサロン1インチオエート。Propaphos j MIPC, Bosalon 1 inch oetoate.

ピレトリン、ケルセン、インキサチオン、サリチオン、
 CYAP 、アミトラズ、カルタップ、 cvpなど
があげられun剤とじてはポリオキシン。
pyrethrin, kelsen, inxathion, salithion,
Examples include CYAP, amitraz, cartap, cvp, and polyoxin as an anti-inflammatory agent.

フサライド、グイホルタン、チオファネートメチル、 
EDDP 、 IBP 、カスガマイシン、ストレフ゛
トマイシン、イングロチオラン、マンネブ、ジネプ、ベ
ノミル、プロペナゾール、トリアジン。
fusaride, guyfortan, thiophanate methyl,
EDDP, IBP, kasugamycin, streftomycin, ingrothiolane, maneb, ginep, benomyl, propenazole, triazine.

TMTD 、 TPN 、キャブタン、プラストサイジ
ンS。
TMTD, TPN, Cabtan, Plasticidin S.

塩基性塩化鋼、塩基i!+:饋酸銅、水酸化第二銅。Basic chloride steel, basic i! +: Copper acetate, cupric hydroxide.

ポリカーバメート、ヒドロキシイソキサゾールなどがあ
げられ、fた除草剤としては、DCMV 。
Examples of herbicides include polycarbamates and hydroxyisoxazole, and DCMV.

DCPA 、シメトリン、ビラゾレート、アトラジン。DCPA, cymetrine, virazolate, atrazine.

DBN 、 IPC、ブタクロール、ニトラゾン、オキ
サシアシン、アロキシジム、 MCCjバラコートジク
ロリド、クロメトキシニル、 CNP 、ペンタシン、
ペンチオカーブ、 CAT 、 MCPエチル、トリフ
ルラリン、 MCPBエチル、ビフェノックス。
DBN, IPC, butachlor, nitrazone, oxacyacin, alloxydim, MCCj baraquat dichloride, clomethoxynil, CNP, pentacine,
Penthiocarb, CAT, MCP ethyl, trifluralin, MCPB ethyl, bifenox.

モリネート、ダゾメットなどがあげられる。Examples include molinate and dazomet.

式(I)を有する化合物の添加率は、主として農薬有効
成分、担体の種類などによっても異なるが、通常2〜2
0重M%程度の添加で有効である。また、他のアニオン
界面活性剤、ノニオン界面活注剤、水浴性無機塩、水溶
性高分子物質(PVA 、 CMC、リグニンスルホン
酸塩など〕などの分散剤との併用も可能である。
The addition rate of the compound having formula (I) varies mainly depending on the agricultural chemical active ingredient, the type of carrier, etc., but is usually 2 to 2.
Addition of approximately 0% by weight is effective. Further, it is also possible to use it in combination with dispersants such as other anionic surfactants, nonionic surfactants, water-based inorganic salts, and water-soluble polymeric substances (PVA, CMC, lignin sulfonate, etc.).

〔実施ガ〕[Implementation Ga]

次に実施例等をあげて本発明を更に具体的に説明するが
、これによって限定されるものではない。なお比較例と
して粉状水相用分散剤として著効を有することが知られ
ているポリオギシアルキレンフェニルエーテル減飲エス
テル塩を使用した。
Next, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited thereto. As a comparative example, a polyoxyalkylene phenyl ether reduced drinking ester salt, which is known to be highly effective as a dispersant for a powdery aqueous phase, was used.

実施例1 フサライド 80部、クレー8部およびドテシルジフェ
ニルエーテルジスルホン酸ジナトリウム塩〔日本乳化剤
四層、Newcol−271A312部を粉砕混合した
後、水20部を加え、押出し造粒機〔不二パウダル@製
、ペンツターEXD m )で造粒し、乾燥後篩別し1
0〜50メツシユの顆粒を得た。
Example 1 After pulverizing and mixing 80 parts of fusaride, 8 parts of clay, and 312 parts of dodecyl diphenyl ether disulfonic acid disodium salt [Nippon Nyukazai 4-layer, Newcol-271A], 20 parts of water was added, and an extrusion granulator [Fuji Paudal@ Pelletized with Penzter EXD m), dried and sieved 1
Granules of 0 to 50 mesh were obtained.

実施例2 NAC85部、ホワイトカーボン2部、クレー3部およ
びドデシルジフェニルエーテルジスルホン酸ジ(1/2
)カルシウム塩 10部を粉砕混合した後、水20部金
加え、押出し造粒機(前出)で造粒し、乾燥後面別し、
10〜50メツシ二の顆粒金得た。
Example 2 85 parts of NAC, 2 parts of white carbon, 3 parts of clay and dodecyl diphenyl ether disulfonic acid di(1/2
) After pulverizing and mixing 10 parts of calcium salt, 20 parts of water and gold were added, and the mixture was granulated using an extrusion granulator (described above). After drying, the surfaces were separated.
10 to 50 pieces of gold granules were obtained.

実施例3 MEP  40部、ホワイトカーボン 50音すおよび
オクチルジフェニルエーテルジスルホン酸ジアンモニウ
ム塩10部を粉砕混合した後、水15部全加え、転勤造
粒機〔栗本鉄工社製、パン型造粒KC)10型〕で造粒
し、乾燥後篩別して10〜50メツシユの顆粒を得た〇 実施例4 ダイホルタン 80部、クレー 10部およびドデシル
ジフェニルエーテルジスルホン酸ビストリエタノールア
ミン塩 10部を粉砕混合した抜水20部を加え、押出
し造粒機(@出)で造粒し、乾燥後面別し10〜50メ
ツシユの顆粒を得たO 実施例5 チオ7アネートメチル 75部、ホワイトカーボン2部
、クレー 11部およびヘキサデシルジフェニルエーテ
ルジスルホン酸ジナトリウム塩12部を粉砕混合した後
、水20部金加え、押出し造粒機(前出〕で造粒し、乾
燥後篩別し10〜50メツシユの顆粒を得之。
Example 3 After pulverizing and mixing 40 parts of MEP, 50 parts of white carbon, and 10 parts of octyldiphenyl ether disulfonic acid diammonium salt, all 15 parts of water were added, and a transfer granulator [manufactured by Kurimoto Iron Works Co., Ltd., pan-type granulator KC] was used. Example 4 80 parts of difortan, 10 parts of clay, and 10 parts of dodecyl diphenyl ether disulfonic acid bistriethanolamine salt were pulverized and mixed to obtain granules of 10 to 50 meshes. Example 5 Thio-7anate methyl 75 parts, white carbon 2 parts, clay 11 parts and hexa After pulverizing and mixing 12 parts of decyl diphenyl ether disulfonic acid disodium salt, 20 parts of water was added and granulated using an extrusion granulator (described above). After drying, the mixture was sieved to obtain 10 to 50 mesh granules.

実施例6 DCPA 50部、ホワイトカーボン5部、クレー33
部およびオクチルジフェニルエーテルジスルホン酸ビス
トリメチルアミン塩12部を粉砕混合した後、水15部
金加え、押出し造粒機(前出って造粒し、乾燥後篩別し
、10〜50メツシユの顆粒を得た。
Example 6 50 parts of DCPA, 5 parts of white carbon, 33 parts of clay
1 part and 12 parts of octyl diphenyl ether disulfonic acid bistrimethylamine salt were pulverized and mixed, 15 parts of water was added, and the mixture was granulated using an extrusion granulator. Ta.

比較例1 フサライド 80部、クレー8部およびドデシルベンゼ
ンスルホン酸ナトリウムff112mk&用して、実施
例1と同様にして顆粒を得た。
Comparative Example 1 Granules were obtained in the same manner as in Example 1 using 80 parts of fusaride, 8 parts of clay, and sodium dodecylbenzenesulfonate ff112mk&.

比較例2 NAC85部、ホワイトカーボン2部、クレー3 部k
 ヨCF E、o、 (20モル)ドデシルフェニルエ
ーテル+I/rceRエステルカルシウム塩10 部k
 使用し、実施例2と同様にして顆粒を得た。
Comparative Example 2 85 parts NAC, 2 parts white carbon, 3 parts clay
YOCF E, o, (20 mol) Dodecyl phenyl ether + I/rceR ester calcium salt 10 parts k
Granules were obtained in the same manner as in Example 2.

比較例3 MEP  40部、ホワイトカーボン 50部ひよびE
、O,(4モル)オクチルフェニルエーテル硫酸エステ
ルアンモニウム塩10部を使用し、実施例3と同様にし
て顆粒會得た。
Comparative Example 3 MEP 40 parts, white carbon 50 parts Hiyoto E
, O, (4 mol) Octyl phenyl ether sulfate ammonium salt was used to prepare granules in the same manner as in Example 3.

比較例4 ダイホルタン 80部、クレー 10部およびドテシル
ベンゼンスルホン酸トリエタノールアミン塩10部を使
用し、実施例4と同様にして顆粒を得た。
Comparative Example 4 Granules were obtained in the same manner as in Example 4 using 80 parts of difortan, 10 parts of clay, and 10 parts of dotesylbenzenesulfonic acid triethanolamine salt.

比坤づと1シリ 5 チオファネートメチル 15部、ホワイトカーボン2m
、りL/−11”liおよびE、O,(15−E:k)
ノニルフェニルエーテル硫酸エステルナ) IJウム塩
 12部を使用し、実施例5と同様にして顆粒を得た。
Hikonzuto 1 silicate 5 thiophanate methyl 15 parts, white carbon 2m
, ri L/-11"li and E, O, (15-E:k)
Granules were obtained in the same manner as in Example 5 using 12 parts of nonylphenyl ether sulfate (IJ) salt.

比較例6 DCPA 50部、ホワイトカーボン5部、クレー33
部およびオクチルベンゼンスルホン酸トリメチルアミン
塩 12部全使用し、実施例6と同様にして顆粒を得た
Comparative Example 6 50 parts of DCPA, 5 parts of white carbon, 33 parts of clay
Granules were obtained in the same manner as in Example 6 except that all 1 part and 12 parts of octylbenzenesulfonic acid trimethylamine salt were used.

〔発明の効果〕〔Effect of the invention〕

次に試験例をあげて本発明の効果を具体的に説明する。 Next, the effects of the present invention will be specifically explained with reference to test examples.

1)崩壊性試験 3度硬水5〇−全直径90のガラス製シャーレに入れた
もの12個金相意し、これを静置して各実施例および比
較例によって造粒した試料5粒づつを入れる。投入直後
から試料が粒形をとどめなくなるまでの時間全5粒につ
いて平均し崩壊時間とした。この値の少さいもの程崩壊
性が優れていることになる。
1) Disintegration test Twelve pieces were placed in a glass petri dish with 3 degree hard water of 50° and a total diameter of 90°, left to stand, and 5 pellets of the sample granulated according to each example and comparative example were added. The time from immediately after the sample was added until the sample no longer retained its particle shape was averaged over all five particles and was defined as the disintegration time. The smaller this value is, the better the disintegrability is.

2)水中分散性試験 3度硬水150−を200−有枠シリンダーに入れたも
の12個を用意し、これに各実施例および比較例によっ
て造粒した試料so、p’i入れて5分間静置する。静
置後30回激しく転倒全繰返し、分散状態を観察する。
2) Dispersibility test in water Prepare 12 cylinders filled with 3 degree hard water (150-200), add samples so and p'i granulated according to each example and comparative example, and let stand for 5 minutes. place After being allowed to stand still, the mixture was violently overturned 30 times and the state of dispersion was observed.

1時間後250メツシユの篩に通し、篩上の残渣物を少
量の水でビーカーに洗い流し、乾燥後残泣物の重量を測
定する。残渣物の重重が少い方がストレーナ−や噴霧器
のノズルをつまらせる障害が少く優れている。
After 1 hour, pass through a 250-mesh sieve, wash the residue on the sieve into a beaker with a small amount of water, and measure the weight of the residue after drying. The lower the weight of the residue, the less the problem of clogging the strainer or sprayer nozzle, which is better.

分散状態の評価は次のようにした。The dispersion state was evaluated as follows.

○:均−分散、△:禾分散、×:凝集 3)懸垂性試験 3度硬水200 d ’i 250 rntの有枠シリ
ンダーに入れたもの12個を用油し、これに各実施例お
よび比較例によって造粒した試料2.51を入れる。次
に3度硬水を追加して25θ−とし5分間静置する。静
置後30回激しく転倒を繰返し再び静置させ、1時間抜
上部よシ225 m/ (9/10容)を静かに吸い収
シ、残りの25−全乾燥恒量(乾燥残分りとし、次式に
よシ悪垂率(鉤を算出した。
○: Uniform dispersion, △: Dispersion, ×: Coagulation 3) Suspension test 12 pieces placed in a framed cylinder of 3 degree hard water 200 d'i 250 rnt were oiled, and each example and comparison was applied to this. Add sample 2.51 granulated according to the example. Next, add 3 degree hard water to make the solution 25θ- and leave it for 5 minutes. After leaving it to stand, it was violently inverted 30 times and left to stand again. Gently suck up 225 m/(9/10 volumes) from the top for 1 hour. The sagging rate (hook) was calculated according to the formula.

懸垂率が大きい程、散布の際に再分散や貴攪拌の操作の
必要がなく、一度の分散で長時間安定な懸濁液が得られ
る。従来の粉状農薬水相物では、通常懸垂率γOq6を
目標に製造されてお9、値に大きい程潰れていることを
示すがこれ以上であれば実用上問題はない。
The larger the suspension ratio, the less redispersion and intensive stirring operations are required during dispersion, and a stable suspension can be obtained for a long time with a single dispersion. Conventional powdered agricultural chemical aqueous phase products are usually manufactured with a suspension ratio of γOq of 6 as the target9, and the larger the value, the more crushed the suspension ratio is, but if it is higher than this, there is no practical problem.

試験結果 上記試験の結果をまとめると下表の如くなる。Test results The results of the above tests are summarized in the table below.

上記試験結果から明らかなように、本発明に係る凝業顆
粒状水相剤組成物は、崩壊性9分散性に潰れるばかシで
なく、懸垂率も極めて高く、長時間安定な懸濁液を与え
るものである。
As is clear from the above test results, the coagulated granular aqueous phase agent composition according to the present invention has a disintegrability of 9 dispersibility, does not collapse, has an extremely high suspension rate, and forms a stable suspension for a long time. It is something to give.

Claims (1)

【特許請求の範囲】 式 ▲数式、化学式、表等があります▼ (式中、Rは炭素数6〜16個のアルキル基を示し、M
はアルカリ金属原子、1価相当のアルカリ土類金属原子
、アンモニウム基、またはアルキル若しくはヒドロキシ
アルキル置換アンモニウム基を示す。)を有する化合物
を含有したことを特徴とする崩壊性、分散性の改良され
た顆粒状水和剤組成物。
[Claims] Formula ▲ Numerical formula, chemical formula, table, etc. ▼ (In the formula, R represents an alkyl group having 6 to 16 carbon atoms, and M
represents an alkali metal atom, a monovalent equivalent alkaline earth metal atom, an ammonium group, or an alkyl- or hydroxyalkyl-substituted ammonium group. ) A granular wettable powder composition with improved disintegrability and dispersibility, characterized by containing a compound having the following properties.
JP23911585A 1985-10-25 1985-10-25 Granular wettable powder composition Pending JPS6299356A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23911585A JPS6299356A (en) 1985-10-25 1985-10-25 Granular wettable powder composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23911585A JPS6299356A (en) 1985-10-25 1985-10-25 Granular wettable powder composition

Publications (1)

Publication Number Publication Date
JPS6299356A true JPS6299356A (en) 1987-05-08

Family

ID=17040017

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23911585A Pending JPS6299356A (en) 1985-10-25 1985-10-25 Granular wettable powder composition

Country Status (1)

Country Link
JP (1) JPS6299356A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003007712A1 (en) * 2001-07-19 2003-01-30 Dsm Ip Assets B.V. Streptomycin-containing granules and process for the preparation thereof
CN106631921A (en) * 2016-11-10 2017-05-10 广东锦昱材料科技有限公司 High-efficiency difunctional anionic surfactant disodium hexadecyl diphenyl ether disulfonate prepared from tetrapolybutene

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003007712A1 (en) * 2001-07-19 2003-01-30 Dsm Ip Assets B.V. Streptomycin-containing granules and process for the preparation thereof
CN106631921A (en) * 2016-11-10 2017-05-10 广东锦昱材料科技有限公司 High-efficiency difunctional anionic surfactant disodium hexadecyl diphenyl ether disulfonate prepared from tetrapolybutene

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