JPS5813504A - Surface coating granular agricultural chemical - Google Patents
Surface coating granular agricultural chemicalInfo
- Publication number
- JPS5813504A JPS5813504A JP11344381A JP11344381A JPS5813504A JP S5813504 A JPS5813504 A JP S5813504A JP 11344381 A JP11344381 A JP 11344381A JP 11344381 A JP11344381 A JP 11344381A JP S5813504 A JPS5813504 A JP S5813504A
- Authority
- JP
- Japan
- Prior art keywords
- agricultural chemical
- water
- carrier
- granular
- chemical active
- 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
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Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】
″本慟−は農−有効成分を粒eai体’DI!IIK被
覆しえ溶脱性のすぐれた農薬着剤〇−法に関すゐもので
あム、 ′
一献KJI薬粒鋼の御−に杜、最−有効成蓚とカオリン
、クレー、Iiミルクベントナイト、白土。[Detailed Description of the Invention] ``This paper relates to a method for coating agriculturally active ingredients on grains of DI!IIK and having excellent leachability as an agricultural chemical adhesive.'' Granular steel, the most effective grains of silk, kaolin, clay, milk bentonite, and white clay.
炭酸カルシクム等各種鉱物質黴聯末と結合剤、崩壊及び
濤脱促迩剤、温展剤として界面活性剤、水**無機成分
、水濤性高分子物質とを渦合し、少量O水で練)′aぜ
て造粒する練シ込与造較法、T。Various mineral mold powders such as calcium carbonate are mixed with surfactants as binders, disintegration and release promoting agents, and warming agents, water**inorganic components, and hydrophobic polymer substances, and a small amount of O water is added. Kneading) 'A method of kneading and granulating by agitation, T.
るいは↑め造粒し九゛粒状纏体着しくは原石を看砕して
篩別し九担体に、上記同様、界面活性鋼中高又は溶媒−
希釈して噴霧被覆する褒面被覆法又は゛造粒担体に會浸
名せる方法等がある。Or the raw stone is crushed and sieved to form a 9-carrier, and the surface-active steel medium or solvent is granulated as above.
There are a surface coating method in which the material is diluted and spray coated, and a method in which a granulated carrier is impregnated with the material.
通常の鋺剤は機械的な圧力中衝撃に対゛して又、熱中[
fK対して崩壊せずに形状を保持し開−でoIIA用後
に於ては容易に崩壊して會有するl&票有効成分をその
生物的効果が最良になるようK11l脱し作用を尭揮す
ることが必要となる。この為に粒@0−造−際しては界
面活性剤、水溶性高分子物質、氷溶−無機化合物等が會
有されるが界面活性剤としてはりグー?・−ホ・酸塩、
シア〜キーールホ号クシネート、アル中ルベンゼンスル
ホネート等のアニオン性界面活性剤、ポリオキシエチレ
ンOアル中ルエーテル、アル中ルアリルエーテル支はエ
ステル類のノーオン性界面活性剤の他、乳化剤@0混金
物が利用される。水溶性高分子物質としてはポリビニル
アルコール、ポリアル中ルダリコール、CMC,MC,
澱物、アクビアβム、トラガントガム、グルカン、デキ
ストラン、ポリビニルピロリド/、にかわ、グリセリド
−とドー命ジエチルセルロース、アルダ/1ljLワV
クス、ゼラチ/、流動パラツイン、セルロースs、tm
ヒトt!中ジプロピルセルロース、トールm、牛脂。Ordinary mulch agents are resistant to mechanical pressure, impact, and heat [
It maintains its shape without disintegrating against fK, and easily disintegrates and interacts with the active ingredient K11L in order to maximize its biological effect and exert its action. It becomes necessary. For this purpose, surfactants, water-soluble polymeric substances, ice-soluble inorganic compounds, etc. are used in the production of grains.・−ho acid salt,
Anionic surfactants such as succinate, rubenzene sulfonate in alcohol, polyoxyethylene O ether in alcohol, and allyl ether in alcohol are used in addition to non-ionic surfactants of esters, as well as emulsifier @0 mixtures. Ru. Water-soluble polymer substances include polyvinyl alcohol, polyalcohol in polyalcohol, CMC, MC,
Starch, Akbia βum, tragacanth gum, glucan, dextran, polyvinylpyrrolid/, glue, glyceride and diethylcellulose, Alda/1ljLwa V
sous, gelati/, liquid paratwin, cellulose S, tm
Human t! Medium dipropyl cellulose, tall m, beef tallow.
シリ;ン油、植物ワークス、植物油、ポリエチレンワッ
クス、ポリアクリル酸塩、ポリマレイン酸塩等が用いら
れて1九。Silicone oil, vegetable works, vegetable oil, polyethylene wax, polyacrylate, polymaleate, etc. are used.
練)込み式造粒法の場合に1tan有効成分の大部分が
粒状体に内蔵されて−るので施用時に11!が崩壊し有
効成分が濤脱して拡散しないと劫果発構に憂らなかう九
)、微粒化し―いという一点が69I丸、*面被覆法に
よる粒剤の製造は、この点改良されて−haか)か−進
法の簡便さから多用されて自たがいくつかO閾■点が参
った。★ず、粒状体01111は轟薬有効威分O執着量
に@変がある。In the case of the kneading type granulation method, most of the 1tan active ingredient is incorporated into the granules, so 1tan! Unless the active ingredient disintegrates and diffuses, there is no need to worry about the deterioration.9) The one point of 69I is that it is difficult to atomize.*The production of granules by the surface coating method has been improved in this respect. -ha?) Because of the simplicity of the -decimal system, it is often used, and some of us have suffered from O threshold ■ points. ★Zu, the granular material 01111 has an @ strange amount of effective force and attachment.
即ち、農薬有効成分−液体の場合には直接噴−して被覆
するか又は上記各種補助剤やssi;と混合して被覆す
るが1粒状体表面が乾燥し丸後、いつまでもぺとり1晶
く、粒体椙亙O結会がみられることが争い、又、農薬有
効成分が徽聯化され九固体の場合には、単独又は他の界
面活性鋼や補#剤と温合して、又は溶媒に溶融し九ルし
て粒状体の表面に噴霧して被覆するが乾燥し九後、農薬
有効成分が艙1析出して剥離し具(なる現象がみられる
ことが多い。That is, in the case of a liquid agricultural chemical active ingredient, it can be sprayed directly to coat it, or it can be coated by mixing it with the various auxiliary agents and SSI; It is disputed that granular O-association is observed, and in the case where the agricultural chemical active ingredient is solidified and solid, it may be used alone or in combination with other surface-active steels or adjuvants, or It is melted in a solvent and sprayed onto the surface of the granules to coat them, but after drying, the active ingredient of the agricultural chemical precipitates out and is often removed by a peeling tool.
本発明者等は、液状の農薬有効成分中1体状貴県有効成
分を粒状体表−に被覆してちぺとり(ことなく、又剥離
することな(結合し、開場に施用すると1には速やかK
il脱する農薬粒剤を得ぺ(種々検討を重ねた結果、有
効成分としては液体及び固体OSg成分を、担体として
は原石’as砕物から篩別し九粒状体友び各種鉱物質黴
場末から造粒された粒状体表面に、水*、a若しく検水
分散性の合成高分子カルボン酸及びその誘導体の被覆を
層成するととによp給金して、農薬有効成分粒状体01
1111中大きさにかかわらず、すぐれ九−出性能をも
つ表面被覆渥農−粒剤を製造すゐことを見いだした。The inventors of the present invention coated the surface of the granular body with a single-form active ingredient in a liquid agricultural chemical active ingredient, bonded it without peeling (bonded), and applied it to an open field. As soon as possible
(As a result of various studies, we found that the active ingredient is a liquid and solid OSg component, and the carrier is a 9-granular material obtained by sifting from crushed raw stones and various minerals from the end of a mold field.) A coating of water*, a, or a water-dispersible synthetic polymer carboxylic acid and its derivatives is layered on the surface of the granulated granules, and then P is added to form agrochemical active ingredient granules 01.
It has been found that a surface-coated agricultural granule with excellent yield performance can be produced regardless of size.
本慟明に於ける合成高分子カルボン酸及びそ011導体
とは、アクリル酸、メタクリル酸、マレイン酸の重合体
てあうて、従つて、又これら重合体OII導体例えば低
級アル中ルエステルア電ド、アルカリ◆属塩、アンモニ
ウム塩及び有機アζン塩を含有する4のである。Synthetic polymeric carboxylic acids and their 011 conductors in this specification include polymers of acrylic acid, methacrylic acid, and maleic acid. ◆ Containing genus salts, ammonium salts and organic amine salts.
これら不飽和カルダン酸はいずれもビニル基を有してお
)、既存全知Oラジカル体上触媒に↓〕重体上て広範I
IO重舎体上与えるがすでに親明し大過〉水に対して溶
解するか若しくは分散すゐ倫農薬有劫威分と良好な相溶
性%−和性をもつ。All of these unsaturated cardanoic acids have a vinyl group), and can be used as catalysts on existing omniscient O radicals.
IO has good compatibility with pesticides, which are dissolved or dispersed in water and have good compatibility.
乾燥後は強度な機械的強度をもつ被膜を形成し、水中で
は迅速Ell欝して界面活性剤など他の補助剤と共に農
薬有効成分を水中に溶出するという機能をもつものであ
る。 。After drying, it forms a film with strong mechanical strength, and has the function of quickly evaporating in water and eluting the active agricultural ingredients together with other adjuvants such as surfactants into water. .
919てここに明示し九不飽和カルl/酸は他のビニル
基を有す為単量体例えばスチレン、酢酸ビニル、塩化ビ
ニル、各種ビニルエーテル化合物と共重合体を形成する
ことがで−るので多種類の被膜を形成する高分子物を誘
導することができる。919 is specified here because it has other vinyl groups and can form copolymers with monomers such as styrene, vinyl acetate, vinyl chloride, and various vinyl ether compounds. Polymers that form many types of films can be derived.
異体的には、lItリアクリル酸、ポリメタクリル酸s
が9マレイン酸、ポリアクリル酸−メタクリル酸、ポリ
アクリル酸−マレイン酸、ポリアクリル蒙アオド、ポリ
マレイン酸−酢酸ビニル及びこれら重合体のナトリクム
、カリクム、アンモニクム塩−有機ア電ン塩等か又部分
ケン化物等が好まし!例として挙げることができる。こ
れら合威萬分千カルボン酸及びその誘導体の一部は造粒
eclIして使用して11象例がみられる0例えば、4
1会昭411’−1町01号は水中崩壊拡展性のすぐれ
た粒を水と共K111合して転−瀝造粒機や押し出し瀝
造°−機によp造粒するもOで612.このようにして
製造され大農薬粒剤は、施用時水中で崩壊して有効成分
が拡散する仁とを特長とする亀のである。Variants include lIt lyacrylic acid, polymethacrylic acid s
9 Maleic acid, polyacrylic acid-methacrylic acid, polyacrylic acid-maleic acid, polyacrylic acid-vinyl acetate, polymaleic acid-vinyl acetate, and sodium, calicum, and ammonicum salts-organic atronic salts of these polymers, etc. Saponified products are preferable! This can be cited as an example. Some of these carboxylic acids and their derivatives have been used as granules in 11 cases. For example, 4
1986-1 Town No. 01 is made by combining grains with excellent disintegration and spreadability in water with K111 and granulating them using a rolling die granulator or an extrusion die granulator. 612. The large pesticide granules produced in this way are characterized by a granule that disintegrates in water upon application, allowing the active ingredients to diffuse.
又、41会昭S鵞−雪10881は1llI&薬同体散
布剤の*Wを粒剤の製造後に上記合成高分子カルボン酸
及びその誘導体Oas末でがおうことによ〕、。In addition, the 41st Eisai Sho-Sen-Sue 10881 is obtained by dissolving *W of the 1llI and pharmaceutical drug dispersant with the above-mentioned synthetic polymer carboxylic acid and its derivative Oas powder after producing the granule].
晴着性能を改嵐しようとする慟明−閤するもので・ある
、 ゛
従うてこれら既存0@@は本発明とはその技術思想を全
く異にするものである。This is an attempt to improve the clear weather performance.Therefore, these existing devices have completely different technical ideas from the present invention.
本発@に係る合成高分子カルボン酸及び七〇、S導体は
その単量体の種類に依存して多種類のものが使用で自る
と共に一般的にはそO重金度は70〜to@oの範囲の
ものが好適である。しかし必゛ ずしもζO@IIK@
定される亀のではない。The synthetic polymeric carboxylic acid and 70, S conductor related to this invention can be used in many types depending on the type of monomer, and generally have a heavy metal content of 70 to 70. A range of o is suitable. But it must be ZushimoζO@IIK@
It is not a turtle that is determined.
これら合成高分子カルボン酸及び誘導体は、Ii体であ
hが被膜形成時には通常!O〜40%O水溶液として液
体又は黴看化され九a薬有効成分ど1和又は111簿さ
れ、更にこれらの温和を容易にならしめる補助剤、fI
I出・拡散促進剤としての界薗活性剤、乳化を促進する
乳化剤と共に粒状担体表両に噴@*れるが混合均一化の
丸め通常ナクター電命ず一、リボン々キサー、ドラム(
キす−等が用いられ先後、乾燥工種を経て粒剤となるも
のである。1:
本Ii@に於いて使用しうる農薬有効−分は殺央剤、s
!曹剤、瞼草剤K11lらずあらゆる種類の農薬K11
l用で自るものである。These synthetic polymeric carboxylic acids and derivatives are in the Ii form and the h form is usually used when forming a film! The active ingredients of the nine-a medicine are contained in a liquid or mold as an aqueous solution of O to 40% O, and furthermore, an adjuvant, fI, which facilitates the softening of these ingredients.
It is sprayed on both sides of the granular carrier together with the Kaizono activator as an I release/diffusion promoter and the emulsifier to promote emulsification.
After that, it is made into granules through a drying process. 1: The effective amount of pesticides that can be used in this Ii @ is the centrifugal agent, s
! All kinds of pesticides K11, not just soda agents and herbicides K11l
It is for personal use.
駿歳剤としては0.8−ジメチル−N−ア七チルホス、
ホロアミドチオエート、0.0−ジメチル−8−7タル
インドメチルジチオホス7エー)、0,0−ジエチル−
8−2−(エチルチオ)エチルホスホ費ジテオエート、
!−り■ルー1−、(L4.!1−)9/ロル7工二ル
)ビニルジメチルホスフェート、冨−イソプロポ中ジフ
ェニルーN−メチルカーバメート、ジメチル(3−メチ
ル−4−ニトロツエニル)テオホスフ” −) s 1
− + 7 ? ルー H−メチルカーバメート、(!
−イソプロピルー4−メチルピリ電ジル−6)−ジエチ
ルチオホスフェート等が挙げられ、殺菌剤としては゛ジ
イソプロδ
ビル−13−ジチオラン−8−〒すデ!9!−マロネ−
)、O,O−シイ、ソプロビルー8−ベンジルチオホス
フェート等
除草剤としては飢4−ジ、クロル7エエルー3−メトキ
シ−4′−エトpツエエルエーテル、S−エチルへキ紫
と)’El−IH−アゼピンー!−カーボテオエート、
意−メチルチオ−也6−ピスーエテルア電ノー8−トリ
アジン、!、6−ジタロルベンゾ品トリトリル−(4−
′クロルベンジル)−N、N−ジエチルチオカーパ57
)、意−クロル−も6−ビス(エチル゛アし0−トドリ
アジン、L4−ジク關ルツエエルー4−ニド諺フェニル
エーテル勤訃4.6−トリクpルフェニルー:4′−二
)W7エエルエーテ、ル、トイソプロビルーシ屯トムン
ゾーテアジアジノン−(4)−意、3−ジオキシド等が
挙げもちるが、これらの例示し大化合物のみKll定1
れゐもOではない。0.8-dimethyl-N-acetylphos,
holamidothioate, 0.0-dimethyl-8-7talindomethyldithiophos 7-ether), 0,0-diethyl-
8-2-(ethylthio)ethyl phosphoroditioate,
! -ri■Lu1-, (L4.!1-)9/Rol7-dimethyl)vinyldimethylphosphate, diphenyl-N-methylcarbamate in isopropyl, dimethyl(3-methyl-4-nitrozenyl)theophosph"-) s 1
−+7? Roux H-methyl carbamate, (!
-Isopropyl-4-methylpyridenyl-6)-diethylthiophosphate, etc., and examples of the disinfectant include "diisopropyl-13-dithiolane-8-de!" 9! -Maroney-
), O, O-cyi, soprobyl-8-benzylthiophosphate, etc. As herbicides, starvation 4-di, chlor7-ether-3-methoxy-4'-ethoptzel ether, S-ethylhekipurple and)'El- IH-Azepine! -carbotheoate,
Meaning-methylthio-also 6-pis-ether-electro-8-triazine,! , 6-ditharolbenzo tritolyl-(4-
'chlorobenzyl)-N,N-diethylthiocarpa 57
), meaning-chlor-also 6-bis(ethyl-0-todryazine, L4-dichloromethyl-4-nido-phenyl ether), Examples include toisopropylene tomonzoteadiazinone-(4)-dioxide, 3-dioxide, etc., but only these large exemplified compounds have a Kll rating of 1.
Rei is not O either.
° 以上会成分−配合割合は*に@定されるべ魯ではな
いが1献に#液体又は徽看末状OI&薬有効成分!−+
黛・%、合成高分子カルlン一及びその誘導体al−1
0%、その他の補助剤o−s%、敏状鶴体残のとと自躯
方が多用で自る。 ′ ・本慟明による粒剤l1l11
方法は、I!来O表面被榎臘造敏法がさの一重−★−適
用することがで自、上述し。° The above ingredients - The blending ratio is not determined by *, but it is #liquid or OI & medicinal active ingredients in one serving! −+
Mayuzumi・%, synthetic polymer carin-1 and its derivative al-1
0%, other adjuvants o-s%, sensitive crane body residue and self-propagation are often used. ' ・Granule l1l11 by Honkyomei
The method is I! The method described above can also be applied to the surface of the surface.
た各成分の任意の配合−合によシlk県有効成分と合成
高分子カルボン酸又は七O鱒導体の水溶液更には界面活
性剤等の補助剤を=緒にして同時に。Arbitrary combinations of each component can be combined simultaneously with an aqueous solution of an active ingredient, a synthetic polymer carboxylic acid or a 70% trout conductor, and an auxiliary agent such as a surfactant.
叉は任意O配舎馴序に従つて温合して濤解若しくは温和
しえものを、すでに鉱物質黴扮末を造粒して得た任−〇
、大きさの粒状担体又社原石を砕石し篩別して得た担体
を各穏呵キ号−中に仕吟み、回転攪拌しクク噴優゛し均
一に被覆させた後、乾燥1横を経て脱水し被膜形成す夕
ものである0、εのようにして得九着状農薬は担体0表
面に合成高分子0@―な被膜中に結合し九lk県有効成
分を有し、充憂な機械的な強度を有して* D s−撃
によ1シ剥−・崩壊するこ。Alternatively, the granular carrier or raw stone of size 0, obtained by granulating the mineral mold powder, is heated according to the arbitrary distribution order. The carrier obtained by crushing and sieving is placed in each sieve, stirred and sprayed to uniformly coat it, and then dried for 1 time and dehydrated to form a film. , ε The 9-pasteurized pesticide is bonded to the surface of the carrier in a synthetic polymer coating, has 9 active ingredients, and has excellent mechanical strength *D One piece peels off and collapses due to an attack.
どがな−、又施用されて水中では速やかEll解して農
薬有効成分を放出し拡散促進して作用するものである。After being applied, it quickly decomposes in water, releasing the active pesticide ingredients and promoting their diffusion.
次に本尭明を異体的に説明する丸めIK箇例を挙け“為
がこれら要論例Kjl定されるものではない。Next, I will give examples of rounding IK that explain this book in a different way.
1要論例L
o、oジメチル−8−(3・メチル@4・エトa7エエ
ル)チオホスフェート3部、ポ゛リオキシエチレンスチ
リルフェニルエーテルとドデシルベンゼンスルホン酸カ
ルシウ≠?混合物1部とポリアクリル酸ソー〆(平均分
子量81.000)10%及びポリメタタリル酸1−ダ
(平均分子量!?@00)10%を含む水溶1111!
s部を均一に温和した後、ナクター建 。1 Essay Example L 3 parts of o,o dimethyl-8-(3.methyl@4.ethyl)thiophosphate, polyoxyethylene styrylphenyl ether and calcium dodecylbenzenesulfonate≠? Aqueous solution 1111 containing 1 part of the mixture and 10% of polyacrylic acid (average molecular weight 81.000) and 10% of polymethacrylic acid (average molecular weight!?@00)!
After uniformly softening the s part, Nachtar construction was performed.
中量−中で、48〜75メツシ、の粒IKII別堕微粒
クレー14!IIIK噴霧して添加し、十分に攪拌して
砿覆し九〇 7o’cz時間の乾燥工程を経て有効成分
3%を含有する微粒剤を得え。Medium weight - Medium, 48 to 75 pieces of grain IKII fallen fine clay 14! IIIK was added by spraying, thoroughly stirred and ground, and a drying process of 907 oz. hours was performed to obtain fine granules containing 3% of the active ingredient.
実施例1
4〜S電クロンKll砕し友l−ナフデルーN−メテル
カーパメー)3部、ポ隻アクリル酸トリエタノールア七
ン塩(平均分子量1111,00G)15%水溶液8部
を均一にfiHL九後、先後−’Isメlり&に篩別し
た微粒クレー91!11にドラムずキサ−中で噴霧して
混合した*丁ot*時間の乾燥工程を経て、有効成分3
%を含有する微粒剤を得え。Example 1 3 parts of 4-S Denkron Kll Krushitomo L-Nafdel N-Metelcarpame) and 8 parts of a 15% aqueous solution of acrylic acid triethanolamine salt (average molecular weight 1111,00G) were uniformly mixed after fiHL nine days. The active ingredient 3 was sprayed and mixed in a drum shaker on the finely divided clay 91!
Obtain microgranules containing %.
喪箇例亀
α0−ジエチル−5−S−<エテルチオ)−エチル−ホ
スホ四ジチオエニト5部、ポリオキシエチレンステリル
フェニルエ′二“テルポリマーとドデシルベンゼンスル
ホン酸カルクウムの混合物8部、ポリメタタリル酸アン
モニウム(平均分子量2九800)の40%水ll1l
液S部を均一に混和した後、ナウターミキサ−中で16
〜3oメVシ&に篩別した海砂II”−部と混合攪拌し
て禎覆しえ、?(11時間の乾燥ニーを経て、有効成分
6%を含有する粒剤を得九・夾箇例本
′クレー43部とベントナイト40部をリグニンスルホ
ン酸ソーダ20%を含有し九本溶液17部と練シ喧ぜ、
押し出し式造着機を用いて直径a8■K11′I11シ
て乾燥し九粒基材s為2部に、ジイソプロピル1.3・
ジチオラン−意−イリデンーマロネー)1部部とスチレ
ン・マレイン酸ソーダ共重合体(モル比l:3.平均分
子量1&!!00)の40%水溶液1!部の混和物を、
転動瀝造粒機中で吸着させて、被顆しえ、フO′e!時
間の乾燥工程を経て、有効成分11!%を含有する粒剤
を得た。Examples: 5 parts of α0-diethyl-5-S-<ethylthio)-ethyl-phosphotetradithioenite, 8 parts of a mixture of polyoxyethylene steryl phenyl ether polymer and calcium dodecylbenzenesulfonate, ammonium polymethatalylate 1 liter of 40% water (average molecular weight 29,800)
After uniformly mixing the liquid S part, mix it in a Nauta mixer for 16 minutes.
Mix and stir with ~300 ml of sifted sea sand II'' and overturn. After drying for 11 hours, a granule containing 6% of the active ingredient was obtained. Example: 43 parts of clay and 40 parts of bentonite were kneaded with 17 parts of a nine-tone solution containing 20% sodium lignin sulfonate;
Using an extrusion-type binding machine, dry the 9-grain base material with a diameter of a8 x K11'I11, add 2 parts of diisopropyl, and add 1.3 x 1.
1 part of 40% aqueous solution of 1 part of dithiolane-ylidene-maloney) and styrene-sodium maleate copolymer (mole ratio l: 3. Average molecular weight 1 &!! 00). of the mixture,
It is adsorbed in a rolling granulator and then granulated. After a long drying process, 11 active ingredients! Granules containing %.
実施例翫
S雫エチル・ヘキサ枠イドロー1g−アゼピン〃−
−1碕チオエート6部、2−メチルチオ−4・・)
一ビスーエチルアミ1−8−)リアジンL5111、ジ
オクチルスルホ号クシネート1部及びポリ酢酸ビニル−
アクリル酸ソーダ共重合体(モル比1:3、平均分子量
44000)の25%水溶液8部を埼−に混和し先後、
ナクター1dPサー中で、l!−32メシシ轟に篩別し
た石灰石SaS部に噴霧して浪合し被覆し九0丁O″c
m時間の乾燥工程を経て、有効成分7.!&%を含有す
る粒剤を得え。Example 1 drop of ethyl hexa-frame hydrochloride 1 g of azepine--1 6 parts of thioate, 2-methylthio-4...) 1-bis-ethylamine 1-8-) riazine L5111, 1 part of dioctyl sulfonate succinate and polyvinyl acetate −
8 parts of a 25% aqueous solution of sodium acrylate copolymer (molar ratio 1:3, average molecular weight 44,000) was mixed in the saline, and then
In Naktar 1dP sir, l! - Spray on the SaS part of the limestone that has been sieved to a depth of 32 mm and coat it with 90 pieces of O''c.
After a drying process of m hours, the active ingredient 7. ! Obtain granules containing &%.
w箇例亀
8−(4−クロルベンジル)−N−N−ジエチルデオカ
ーパメート丁部、冨、4.@)リクロルフエエルー4−
二ト四フェニルエーテル@IE、ポ97/9ル酸ソーダ
、メタクリル酸ソーダ共重合体(4ル比lX!、平均分
子量4亀000)の30%水溶液15藻を均−Kfi和
した後、ナラターンキサ−中で、12〜S!メータ&に
篩別した炭カル771−に噴霧して被覆しえ、70′c
!時間の乾燥工程を経て有効成分13%を含有する粒剤
を得た。Examples 8-(4-chlorobenzyl)-N-N-diethyldeocarpamate Tobe, Tomi, 4. @)Liclor Fueru 4-
After homogenizing 15 algae of a 30% aqueous solution of dito-tetraphenyl ether @IE, sodium poly(97/9), and sodium methacrylate copolymer (4 lx ratio, average molecular weight 4,000), Naratanxa - Inside, 12~S! It can be coated by spraying on charcoal 771- which has been sieved to 70'c.
! After a long drying process, granules containing 13% of the active ingredient were obtained.
上記実施例の剥離試験及び溶脱試験の結果を次に示す。The results of the peel test and leaching test of the above examples are shown below.
を剥離試験結果
(i)方 法
試験法は全農法による剥離率算出法に基づいた即ち
試料粒剤又は微粒剤101を下図の如きグラスフィルタ
ー(11G!グラスフイルター使用)に入れすべての部
分を接続した後、風f”Winの割合で2分間空気を通
じる。その後ダラスフィルター内に残9九試料を回収、
秤量して次式によシ剥離率を算出、!囲(〉返しの平均
値讐求めた。Peeling test results (i) Method The test method is based on the peeling rate calculation method by Zennogho, that is, put the sample granule or fine granule 101 into a glass filter as shown in the figure below (11G! Glass filter used) and connect all parts. After that, air was passed for 2 minutes at the rate of wind f”Win.Then, the remaining 99 samples were collected in the Dallas filter.
Weigh it and calculate the peeling rate using the following formula! The average value of the return was calculated.
槍)結 果
上記O如〈実施例1〜60粒剤ば全て剥離率O%であり
友、即ち結合性に富んだ結果となう九。The results were as above (Examples 1 to 60 granules all had a peeling rate of 0%, that is, the results were rich in bonding properties).
am脱試験締果
(1)方 法
SOO*のトールビーカーにto声oイオン交換水WO
O−を入れ1粒剤5frを投入して20℃で意4時間放
置し丸、この試験液を12sメヅシ&O箇で一過し、更
に!!″・0−のイオン交換卜
水で洗滌し、P液を合して’!505gに定容した。am removal test results (1) Method: Pour ion-exchanged water into a tall beaker of SOO*.
Add O-, add 1 tablet 5fr, leave it at 20℃ for 4 hours, pass this test solution through 12s of medicine & O, and then! ! It was washed with ion-exchanged water of 0-1, and P solution was combined to give a constant volume of 505 g.
その10−を分堆し農薬残留分析法(ソフトサイエンス
社、昭1055都)K準するガスクシマドグラフィーに
よシ、各有効成分の定量を行つ溶脱車軸一定量値神)
X 11 S O/ !! t X表示有効成分軸
(幻結 果
113!S−エチルへキすヒドロ−111−7−に’ビ
ン・−1−カーボチオエート
東288−メチルチオ−4・6−ピスーエチノ
ルーξ番−8−)リアジン
宣\
asss−(4−クロoベンジA−)−N、N−ジエテ
ルテオカーパメート
)[4fL4.@−)リクロルフェニルー4′−二トロ
フェニルエーテル
以上の結果、実施例はいずれも機械的衡機に対して、形
状を十分に保持すると共に、水中に於ける溶脱率も十分
に高い粒剤であることが明らかである。The leached axle is used to quantify each active ingredient using gas chromatography based on Pesticide Residue Analysis Method (Soft Science Co., Ltd., 1985).
X 11 SO/! ! t Riazine Asss-(4-ChloobendiA-)-N,N-Dietherteocarpamate) [4fL4. @-) Lichlorphenyl-4'-nitrophenyl ether As a result, all of the examples showed granules that sufficiently retained their shape against mechanical balance and had a sufficiently high leaching rate in water. It is clear that
、I′−
手続補正書(試)
L事件の表示 昭和S6年特許願第113441号〜2
発明の名称 表面被覆型粒状農薬
&補正をする者
昭和56年11月24日(発送日)
&補正の対象 明細書の[発明の詳細な説明]の欄及
び[図面Jの記載。, I'- Procedural Amendment (Trial) Indication of Case L 1939 Showa S6 Patent Application Nos. 113441-2
Title of the invention Surface-coated granular pesticide & Person making the amendment November 24, 1980 (Date of shipment) & Subject of amendment The [Detailed Description of the Invention] section of the specification and the description of [Drawing J].
a補正の内容 明細書第14頁の図面の削除。Contents of amendment a: Deletion of the drawing on page 14 of the specification.
(1)明細書第14頁の図面を削除する。(1) Delete the drawing on page 14 of the specification.
(2) 仝 17頁4行く「4、図面の簡単な説明
」の項を設ける。(2) Provide a section titled ``4. Brief explanation of the drawings'' on page 17, line 4.
(31明細書17頁4厚や欄K
「図面(1)は側面図である。図中
(1)・・・・・・・・・・・・・・・・・・ コンプ
レッサー(2)・・・・・・・・・・・・・・・・・・
マノメーター(31・ 連結管(育種■=)
(4)・・・・・・・・・・・・・・・・・・ 11σ
鬼グラスフイルター(6ト・・・・・・・・・・・・・
・・・・ アダプ^−(6)・・・・・・・・・・・・
・・・・・・補集風(7)・・・・・・・・・・・・・
・・・・・ バッグフィルターを示す。」 ゛
を挿入する。(31 Specification page 17 4 Thickness and Column K "Drawing (1) is a side view. In the figure (1)......... Compressor (2)...・・・・・・・・・・・・・・・・・・
Manometer (31・ Connecting pipe (breeding ■=) (4)・・・・・・・・・・・・・・・ 11σ
Oni glass filter (6t...)
・・・・Adapt^−(6)・・・・・・・・・・・・
・・・・・・Supplementary style (7)・・・・・・・・・・・・・・・
... Indicates a bag filter. ” Insert ゛.
(4) 別紙として図面を記載・する。(4) Describe the drawing as a separate sheet.
Claims (1)
酸、メタクリル駿、マレイ”/酸及びそのエステル類又
は塩類から選ばれ九単量体を重合して1にゐ水溶性又は
水分散性の生成物を使用して被覆することを特徴と子ゐ
表−砿an麺状最−0□The liquid is made into a mold and the active ingredients of the pesticide are polymerized with nine monomers selected from acrylic acid, methacrylic acid, and their esters or salts to make them water-soluble or water-dispersible. Characterized by coating using the product of
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11344381A JPS5813504A (en) | 1981-07-16 | 1981-07-16 | Surface coating granular agricultural chemical |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11344381A JPS5813504A (en) | 1981-07-16 | 1981-07-16 | Surface coating granular agricultural chemical |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5813504A true JPS5813504A (en) | 1983-01-26 |
Family
ID=14612349
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11344381A Pending JPS5813504A (en) | 1981-07-16 | 1981-07-16 | Surface coating granular agricultural chemical |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5813504A (en) |
Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61282301A (en) * | 1985-06-07 | 1986-12-12 | Otsuka Chem Co Ltd | Slow-releasing granular agricultural chemical composition and production thereof |
JPS6340743A (en) * | 1986-08-04 | 1988-02-22 | Central Glass Co Ltd | Easy-to-temper glass composition |
JPH03187946A (en) * | 1989-11-16 | 1991-08-15 | Libbery Owens Ford Co | Infrared and ultraviolet ray absorbing green glass and window glass and window material for vehicular use |
US5380685A (en) * | 1992-03-18 | 1995-01-10 | Central Glass Company, Ltd. | Bronze-colored infrared and ultraviolet radiation absorbing glass |
JP2007308413A (en) * | 2006-05-17 | 2007-11-29 | Nippon Nohyaku Co Ltd | Pesticide granular preparation and method for producing the same |
US8320724B2 (en) | 2009-01-20 | 2012-11-27 | Sumitomo Electric Industries, Ltd. | Optical communication system and arrangement converter |
CN103080797A (en) * | 2010-08-30 | 2013-05-01 | 住友电气工业株式会社 | Multicore optical fiber |
US8447156B2 (en) | 2009-01-19 | 2013-05-21 | Sumitomo Electric Industries, Ltd. | Multi-core optical fiber |
US8687931B2 (en) | 2009-01-19 | 2014-04-01 | Sumitomo Electric Industries, Ltd. | Optical fiber |
US20160213000A1 (en) * | 2013-09-26 | 2016-07-28 | Basf Agrochemical Products B.V. | Method for Controlling Weeds in Sugar Cane Plantations |
US10375959B2 (en) | 2015-01-22 | 2019-08-13 | BASF Agro B.V. | Ternary herbicidal combination comprising saflufenacil |
US10813356B2 (en) | 2015-07-10 | 2020-10-27 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and dimethenamid |
US10897898B2 (en) | 2015-07-10 | 2021-01-26 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and acetochlor or pretilachlor |
US10980232B2 (en) | 2015-07-10 | 2021-04-20 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and pyroxasulfone |
US11116213B2 (en) | 2015-07-10 | 2021-09-14 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and pethoxamid |
US11206827B2 (en) | 2015-07-10 | 2021-12-28 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and specific quinolinecarboxylic acids |
US11219212B2 (en) | 2015-07-10 | 2022-01-11 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and imazamox |
US11291206B2 (en) | 2015-07-10 | 2022-04-05 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and specific pigment synthesis inhibitors |
US11517018B2 (en) | 2015-07-10 | 2022-12-06 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and saflufenacil |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4872338A (en) * | 1971-12-28 | 1973-09-29 |
-
1981
- 1981-07-16 JP JP11344381A patent/JPS5813504A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4872338A (en) * | 1971-12-28 | 1973-09-29 |
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0257047B2 (en) * | 1985-06-07 | 1990-12-03 | Ootsuka Kagaku Kk | |
JPS61282301A (en) * | 1985-06-07 | 1986-12-12 | Otsuka Chem Co Ltd | Slow-releasing granular agricultural chemical composition and production thereof |
JPS6340743A (en) * | 1986-08-04 | 1988-02-22 | Central Glass Co Ltd | Easy-to-temper glass composition |
JPH0433743B2 (en) * | 1986-08-04 | 1992-06-03 | Central Glass Co Ltd | |
JPH03187946A (en) * | 1989-11-16 | 1991-08-15 | Libbery Owens Ford Co | Infrared and ultraviolet ray absorbing green glass and window glass and window material for vehicular use |
US5380685A (en) * | 1992-03-18 | 1995-01-10 | Central Glass Company, Ltd. | Bronze-colored infrared and ultraviolet radiation absorbing glass |
JP2007308413A (en) * | 2006-05-17 | 2007-11-29 | Nippon Nohyaku Co Ltd | Pesticide granular preparation and method for producing the same |
US8687931B2 (en) | 2009-01-19 | 2014-04-01 | Sumitomo Electric Industries, Ltd. | Optical fiber |
US8447156B2 (en) | 2009-01-19 | 2013-05-21 | Sumitomo Electric Industries, Ltd. | Multi-core optical fiber |
US8655131B2 (en) | 2009-01-19 | 2014-02-18 | Sumitomo Electric Industries, Ltd. | Multi-core optical fiber |
US8320724B2 (en) | 2009-01-20 | 2012-11-27 | Sumitomo Electric Industries, Ltd. | Optical communication system and arrangement converter |
US8718429B2 (en) | 2010-08-30 | 2014-05-06 | Sumitomo Electric Industries, Ltd. | Multicore optical fiber |
CN103080797A (en) * | 2010-08-30 | 2013-05-01 | 住友电气工业株式会社 | Multicore optical fiber |
US8867881B2 (en) | 2010-08-30 | 2014-10-21 | Sumitomo Electric Industries, Ltd. | Multicore optical fiber |
US20160213000A1 (en) * | 2013-09-26 | 2016-07-28 | Basf Agrochemical Products B.V. | Method for Controlling Weeds in Sugar Cane Plantations |
US10375959B2 (en) | 2015-01-22 | 2019-08-13 | BASF Agro B.V. | Ternary herbicidal combination comprising saflufenacil |
US10813356B2 (en) | 2015-07-10 | 2020-10-27 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and dimethenamid |
US10897898B2 (en) | 2015-07-10 | 2021-01-26 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and acetochlor or pretilachlor |
US10980232B2 (en) | 2015-07-10 | 2021-04-20 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and pyroxasulfone |
US11116213B2 (en) | 2015-07-10 | 2021-09-14 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and pethoxamid |
US11206827B2 (en) | 2015-07-10 | 2021-12-28 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and specific quinolinecarboxylic acids |
US11219212B2 (en) | 2015-07-10 | 2022-01-11 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and imazamox |
US11291206B2 (en) | 2015-07-10 | 2022-04-05 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and specific pigment synthesis inhibitors |
US11517018B2 (en) | 2015-07-10 | 2022-12-06 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and saflufenacil |
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