JPH11199416A - Granular soil treatment agent for controlling organism - Google Patents

Granular soil treatment agent for controlling organism

Info

Publication number
JPH11199416A
JPH11199416A JP378598A JP378598A JPH11199416A JP H11199416 A JPH11199416 A JP H11199416A JP 378598 A JP378598 A JP 378598A JP 378598 A JP378598 A JP 378598A JP H11199416 A JPH11199416 A JP H11199416A
Authority
JP
Japan
Prior art keywords
component
azide
weight
parts
water
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.)
Withdrawn
Application number
JP378598A
Other languages
Japanese (ja)
Inventor
Koji Fujii
孝司 藤井
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.)
Teijin Ltd
Original Assignee
Teijin Chemicals 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 Teijin Chemicals Ltd filed Critical Teijin Chemicals Ltd
Priority to JP378598A priority Critical patent/JPH11199416A/en
Publication of JPH11199416A publication Critical patent/JPH11199416A/en
Withdrawn legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain in high efficiency the subject soil treatment agent with high commodity value as an agrochemical by including a specific azide compound in high concentrations, an extender, and a specific binder. SOLUTION: This soil treatment agent is obtained by including (A) 10-70 wt.% of an azide compound capable of producing hydrogen azide when decomposed, (B) 30-90 wt.% of an extender, and (C) 1-25 pts.wt. based on 100 pts.wt. of the components A+B, of a binder 200-1,200 ml/100 g in water absorption in the weight ratio C/A of 0.1-1.0; wherein the component A is pref. a compound hydrolyzable when subjected to moisture action, specifically being sodium azide or the like; the component B is pref. talc, pyrophyllite-based agalmatolite clay, Zeeklite, calcium carbonate or the like; and the component C is pref. pregelatinized modified starch, a carboxymethylcellulose alkali salt or the like.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、増量剤、分解によ
りアジ化水素を発生し得るアジ化化合物、及び吸水量が
特定である結合剤からなる生物防除用粒状土壌処理剤に
関する。更に詳しくは作業中の安全を確保し、土壌への
散布を均質かつ効果的に実施でき、更に農薬としての効
果を効率的に発揮する生物防除用土壌処理剤において、
製造効率に優れ、農薬としての商品価値の高い生物防除
用粒状土壌処理剤に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a granular soil treatment agent for biological control comprising a bulking agent, an azide compound capable of generating hydrogen azide by decomposition, and a binder having a specific water absorption. More specifically, a biocontrol soil treatment agent that ensures safety during work, can perform spraying on the soil homogeneously and effectively, and also efficiently exhibits the effect as a pesticide,
The present invention relates to a granular soil treatment agent for biological control having excellent production efficiency and high commercial value as an agricultural chemical.

【0002】[0002]

【従来の技術】近年、土壌中の病害虫および作物の生育
をいちじるしく障害させる雑草の防除のために、効果的
な土壌処理剤が要望されている。既知のDD剤(有効成
分、1,3−ジクロルプロペン)、ホスチアゼート剤
(有効成分、ブチル−O−エチル−2−オキソ−1,3
−チアゾリジン−3−イルホスホノチオアト)は土壌中
に生息する線虫には有効であるが土壌病原菌及び雑草の
防除には効果がなく、ダゾメット剤(有効成分、3,5
−ジメチルテトラヒドロ−2H−1,3,5−チアジアジ
ン−2−チオン)は、線虫及び病原菌には有効であるが
雑草防除には十分な効果を示さず、さらには土壌のもつ
水分含有量の高低により薬効の発揮度や作物への薬害に
バラツキが出る欠点をもっている。
2. Description of the Related Art In recent years, there has been a demand for an effective soil treatment agent for controlling weeds that significantly impair the growth of pests and crops in soil. Known DD agent (active ingredient, 1,3-dichloropropene), phosthiazate agent (active ingredient, butyl-O-ethyl-2-oxo-1,3)
-Thiazolidine-3-ylphosphonothioato) is effective against nematodes living in soil, but is not effective in controlling soil pathogens and weeds. Dazomet (active ingredient 3,5)
-Dimethyltetrahydro-2H-1,3,5-thiadiazin-2-thione) is effective against nematodes and pathogens, but does not show sufficient effect for controlling weeds. It has the disadvantage that the degree of efficacy and the phytotoxicity to crops vary depending on the height.

【0003】一方、分解によりアジ化水素を発生し得る
アジ化化合物、例えばアジ化塩類は、それを圃場に投薬
する時、土壌中で容易に加水分解を受けて気体状のアジ
化水素を生成させ、かかる気体状のアジ化水素が土壌中
の病害虫や雑草の防除に卓効を示すことが知られてい
る。かかる事実よりかかるアジ化化合物を用いる土壌処
理は、土壌中の病害虫および雑草の広範囲な防除に有効
な手段であるとみなされている(Can.J.Micr
obiol.、565−570(1974))。
On the other hand, an azide compound which can generate hydrogen azide by decomposition, for example, azide salts, is easily hydrolyzed in soil when administered to a field to produce gaseous hydrogen azide. It has been known that such gaseous hydrogen azide has excellent effect on controlling pests and weeds in soil. Based on this fact, soil treatment using such azide compounds is regarded as an effective means for controlling a wide range of pests and weeds in soil (Can. J. Micr).
obiol. 565-570 (1974)).

【0004】一般に、これらの土壌処理剤は、効果的で
かつ安定化された防除成果を得るだけでなく、より簡便
でかつ安全な作業効果を得る目的で製剤化が行われる。
これらの製剤化の工夫には、有効成分の物理化学的特性
を十分に生かすことによって最適な農薬剤型を定めるこ
とが行われている。例えば、DD剤は有機溶媒に易溶な
ことからその剤型は油剤として調製せられ、かかる油剤
は分注機の助けを受けて土壌深く注入することによって
均一拡散ができるようになっている。またダゾメット剤
の有効成分は常温で固体であることから固形製剤とさ
れ、更に圃場への均一散布をより確実なものにするため
に微細化された粒剤として調製されている。これらが示
すように土壌処理剤の剤型は、その有効成分の持つ物理
化学的特性を最大限に活用した製剤形態が選択される。
[0004] In general, these soil treating agents are formulated not only to obtain effective and stabilized control results, but also to obtain simpler and safer working effects.
In devising these formulations, the most appropriate physicochemical properties of the active ingredient are fully utilized to determine the optimal agricultural chemical type. For example, since the DD agent is easily soluble in an organic solvent, its dosage form is prepared as an oil, and such an oil can be uniformly diffused by injecting deep into the soil with the aid of a dispenser. The active ingredient of the dazomet preparation is a solid preparation because it is solid at room temperature, and is prepared as finely divided granules to further ensure uniform application to the field. As shown by these, as the dosage form of the soil treatment agent, a preparation form that maximizes the physicochemical properties of the active ingredient is selected.

【0005】分解によりアジ化水素を発生し得るアジ化
化合物、例えばアジ化塩類においても、アジ化塩類の水
溶解度が高いとの物理化学的特性を生かすことにより、
高濃度の水溶液の液剤として調合して、そのまま投薬さ
れる場合もあるが、一般に土壌処理剤を投薬する作業に
は粒剤が望まれている。粒剤は投薬作業おける有効成分
の粉立ちや飛散がなくその取り扱いや計量が容易である
と共に、長期間の貯蔵、保存も簡便である等の利点を有
するためである。そのためいったんアジ化塩類の濃厚水
溶液を調合後、吸収型あるいは吸着型の粒状増量剤に吸
収あるいは吸着させて、粒剤とする粒状化技術が知られ
ている。しかしながらこの製造技術はアジ化塩類が低濃
度領域のものに止まる問題があり、実用上十分とはいえ
なかった。
Azide compounds which can generate hydrogen azide by decomposition, for example, azide salts, also make use of the physicochemical properties that the azide salts have high water solubility.
In some cases, the composition may be prepared as a solution of a high-concentration aqueous solution and administered as it is. However, granules are generally desired for the operation of administering the soil treating agent. Granules are advantageous because they do not cause powdering or scattering of the active ingredient in the administration operation, are easy to handle and measure, and are easy to store and store for a long period of time. Therefore, there is known a granulation technique in which a concentrated aqueous solution of an azide salt is once prepared and then absorbed or adsorbed by an absorption-type or adsorption-type granular extender to obtain a granule. However, this production technique has a problem that the azide salt is limited to a low concentration region, and is not sufficiently practical.

【0006】本願出願人は、かかる問題を解決すべく、
増量剤、分解によりアジ化水素を発生し得るアジ化化合
物及び水溶性結合剤からなる生物防除用組成物を既に提
案している(特開平8−295610号公報)。しかし
ながら、かかる組成物はかかるアジ化化合物を高濃度に
含有できるものの、粒剤を製造する際にはかかる水溶性
化合物を一旦水に溶解した上で、かかる増量剤等の混合
物に添加しないと安定した粒剤の製造が困難であり、更
に造粒品同士が付着し易いため、塊状分が生成し易く次
工程の整粒工程において予め塊状分をほぐす等の必要が
あり製造効率に劣る部分があった。更に整粒工程後得ら
れた粒剤は形状の崩れたものが含まれており、より形状
のそろった商品価値の高い粒剤が望まれるようになって
いる。すなわち商品価値のより高い粒剤を効率よく得る
ことが望まれているものの、従来の方法では十分といえ
るものではなかった。
[0006] The applicant of the present application has sought to solve such a problem.
A biocontrol composition comprising a bulking agent, an azide compound capable of generating hydrogen azide by decomposition, and a water-soluble binder has already been proposed (JP-A-8-295610). However, such compositions can contain such azide compounds at high concentrations, but when producing granules, such water-soluble compounds must be dissolved in water once and then added to a mixture of such bulking agents and the like. It is difficult to manufacture granules, and the granules are easily adhered to each other, so that agglomerates are likely to be generated and it is necessary to loosen the agglomerates in advance in the next sizing step, and there are parts where production efficiency is poor. there were. Furthermore, the granules obtained after the sizing step include those having a deformed shape, and granules having a more uniform shape and high commercial value have been demanded. That is, although it is desired to efficiently obtain granules having higher commercial value, the conventional methods have not been sufficient.

【0007】一般に押出造粒、特に湿式造粒による成型
物たる粒剤は、予め粒剤の原材料たる各種成分及び必要
に応じて更に水を混合した湿潤粉末を、かかる湿潤粉体
中の固体相、液体相及び気体相の割合が成型に適した領
域となるよう調整し成型される。かかる割合が成型条件
の可否の鍵となっており、成型に適した割合を安定的に
保持することにより、かかる押出造粒が安定に保たれ、
目的とする粒剤を収率よく得ることが可能となる。
In general, a granule as a molded product by extrusion granulation, particularly wet granulation, is prepared by mixing a wet powder obtained by previously mixing various components as raw materials of the granule and, if necessary, further water with a solid phase in the wet powder. The ratio of the liquid phase and the gas phase is adjusted so as to be in a region suitable for molding, and then molded. Such a ratio is the key to the feasibility of molding conditions, and by stably maintaining a ratio suitable for molding, such extruded granulation is stably maintained,
It is possible to obtain the desired granules in good yield.

【0008】しかしながら成形時の摩擦熱や粒剤の温度
上昇等といった製造環境の影響により、かかる水溶性粉
末原料が水溶解現象等を起こすため、当初成型に適した
かかる割合が変化し安定に保持されなくなる。その結
果、成型不良あるいは造粒物自体の再付着が起こり、目
的とする粒剤を得ることが困難となり、結果的には製品
収率不良に陥る。
However, such a water-soluble powder raw material causes a water dissolution phenomenon due to the influence of the manufacturing environment such as frictional heat during molding and a rise in the temperature of the granules. Will not be. As a result, molding defects or reattachment of the granules themselves occur, making it difficult to obtain the desired granules, resulting in poor product yield.

【0009】水溶性の高い粉末原料は微粉になればなる
ほど少量の練合水分に容易に溶解するために、成型の適
正比率の水分量を定めることが難しく、標準的な成型条
件を定めることが困難になる。溶解度の影響を受けるこ
れらの現象は一般には造粒時の「熱軟化現象」として知
られ、この影響を回避するために組成物構成やその配合
割合のみならず温度管理や製造条件に種々の工夫がこら
されているものの十分に満足できるものではなかった。
Since powdery materials having high water solubility are easily dissolved in a small amount of kneading water as the powder becomes finer, it is difficult to determine an appropriate amount of water for molding, and it is difficult to determine standard molding conditions. It becomes difficult. These phenomena affected by solubility are generally known as "thermal softening phenomena" during granulation. To avoid this effect, various measures must be taken not only for the composition of the composition and its mixing ratio, but also for temperature control and manufacturing conditions. Although it was broken, it was not satisfactory enough.

【0010】すなわち、分解によりアジ化水素を発生し
得るアジ化化合物、特に水溶性の高いアジ化塩類を、特
に従来の農薬の慣用造粒技術である湿式押出造粒技術で
粒剤化する際、かかるアジ化化合物の持つ高い水溶解度
特性のために生じる成形時の熱軟化現象を防止した、安
定した製造技術は確立しておらず、かかる問題の解決が
要望されていた。
That is, when an azide compound capable of generating hydrogen azide by decomposition, particularly a highly water-soluble azide salt, is granulated by a wet extrusion granulation technique, which is a conventional granulation technique for conventional agricultural chemicals. However, a stable production technique for preventing the thermal softening phenomenon at the time of molding caused by the high water solubility characteristic of such azide compounds has not been established, and a solution to such a problem has been demanded.

【0011】[0011]

【発明が解決しようとする課題】本発明の目的は、分解
によりアジ化水素を発生し得るアジ化化合物、特にアジ
化塩類を高濃度に含有し、かつ安定して製造できる生物
防除用粒状土壌処理剤を提供することにある。更に詳し
くは押出造粒技術を用いて生物防除用組成物を粒状化す
る際、含有する水分の影響を受けることなく、安定して
製造できる生物防除用粒状土壌処理剤を提供し、併せて
粒剤化による利点を提供することにある。
SUMMARY OF THE INVENTION An object of the present invention is to provide a granular soil for biological control which contains a high concentration of an azide compound which can generate hydrogen azide by decomposition, particularly azide salts, and which can be stably produced. It is to provide a processing agent. More specifically, when granulating a composition for biological control using extrusion granulation technology, the present invention provides a granular soil treatment agent for biological control that can be stably manufactured without being affected by the water content. The advantage of the present invention is to provide the advantages of the formulation.

【0012】本発明者は、前記目的を達成するため鋭意
研究を重ねた結果、増量剤、分解によりアジ化水素を発
生し得るアジ化化合物及び吸水量が特定範囲である結合
剤からなる組成物がアジ化化合物を高濃度に含有しつ
つ、かつ製造効率に優れ、農薬としての商品価値の高い
生物防除用粒状土壌処理剤を製造するのに好適であるこ
とを見出し、本発明の生物防除用粒状土壌処理剤を完成
するに至った。
The present inventors have conducted intensive studies to achieve the above object, and as a result, have found that a composition comprising a bulking agent, an azide compound capable of generating hydrogen azide by decomposition, and a binder having a water absorption in a specific range. Contains azide compound at high concentration, and is excellent in production efficiency, and found to be suitable for producing a granular soil treatment agent for biological control having high commercial value as an agricultural chemical, and for the biological control of the present invention. The granular soil treatment agent was completed.

【0013】[0013]

【課題を解決するための手段】すなわち、本発明によれ
ば増量剤、分解によりアジ化水素を発生し得るアジ化化
合物及び吸水量が特定範囲である結合剤からなる生物防
除用粒状土壌処理剤が提供される。
That is, according to the present invention, a granular soil treating agent for biological control comprising a bulking agent, an azide compound capable of generating hydrogen azide by decomposition and a binder having a specified amount of water absorption. Is provided.

【0014】本発明におけるA成分として使用するアジ
化水素を発生し得るアジ化化合物としては、水分の作用
を受けて加水分解する化合物が望ましく、例えばアジ化
塩、特にアルカリ金属塩又はアルカリ土類金属塩が好ま
しく、具体的にはアジ化ナトリウム、アジ化カルシウム
及びアジ化バリウム等が用いられるが、特にアジ化ナト
リウムが好ましい。
As the azide compound capable of generating hydrogen azide used as the component A in the present invention, a compound which hydrolyzes under the action of moisture is desirable, for example, an azide salt, particularly an alkali metal salt or an alkaline earth salt. Metal salts are preferred, and specific examples include sodium azide, calcium azide, barium azide, and the like, with sodium azide being particularly preferred.

【0015】本発明におけるB成分として使用する増量
剤としては、農業製剤用として一般に使用される増量剤
のうち、本発明のA成分にかかるアジ化化合物に対して
不活性である鉱物質の微粉体である。かかる増量剤とし
ては、例えばタルク、セリサイト、ケイ石、ケイ砂、パ
イロフィライト系ろう石クレー、ジークライト、ゼオラ
イト、炭酸カルシウム、ケイソウ土、消石灰等が挙げら
れる。またかかる増量剤の粒径は、平均粒径が5〜50
μmのものが目的とする均質な粒剤をより製造しやすい
ので好ましく使用できる。
The extender used as the component B in the present invention includes, among extenders generally used for agricultural preparations, fine powders of mineral substances which are inert to the azide compound according to the component A of the present invention. Body. Examples of such extenders include talc, sericite, silica stone, silica sand, pyrophyllite-based pyroxene clay, ziglite, zeolite, calcium carbonate, diatomaceous earth, slaked lime, and the like. In addition, the particle size of such an extender is preferably 5 to 50.
μm particles can be preferably used because the desired homogeneous granules can be more easily produced.

【0016】好ましい増量剤としては、タルク、パイロ
フィライト系ろう石クレー、ジークライト、炭酸カルシ
ウム、消石灰を挙げることができる。また必要に応じ
て、更に水溶性を示すアルカリ性物質を適当量添加する
ことも可能である。水溶性を示すアルカリ性物質として
は、アルカリ金属塩、アルカリ土類金属塩等を挙げるこ
とができる。更に本発明のB成分は単独の使用のみなら
ず、必要に応じて2以上を混合しての使用も可能であ
る。
Preferred extenders include talc, pyrophyllite-based limestone clay, ziglite, calcium carbonate, and slaked lime. If necessary, an appropriate amount of a water-soluble alkaline substance can be added. Examples of the water-soluble alkaline substance include alkali metal salts and alkaline earth metal salts. Further, the component B of the present invention can be used not only alone, but also as a mixture of two or more as necessary.

【0017】本発明におけるC成分として使用する結合
剤としては、吸水量が200〜1200ml/100g
である化合物である。
The binder used as the component C in the present invention has a water absorption of 200 to 1200 ml / 100 g.
Is a compound.

【0018】本発明における吸水量とは、JIS K−
5101の規定する「吸油量の測定方法」の測定条件に
準じて行われるものである。すなわち、ガラス板上の試
料にビュレットから1〜数滴ずつ蒸留水を滴下し、その
都度金属ヘラで十分に練り合わせ、滴下及び練り合わせ
の操作を繰り返し試料全体が軟化し、流動化し始める水
分量を求め、試料100g当たりに対する水分量として
算出したものである。すなわち金属ヘラでラセン形に巻
き起こされる程度になった時、ラセン形に巻き起こされ
ないものでは、蒸留水の1滴で急激に軟らかくなり、ガ
ラス板に粘りつく直前の水分量を求め算出したものであ
る。
The water absorption in the present invention is defined by JIS K-
The measurement is performed in accordance with the measurement conditions of the “method for measuring oil absorption” specified in 5101. That is, distilled water is dropped from the burette to the sample on the glass plate by one to several drops at a time, and each time the mixture is sufficiently kneaded with a metal spatula, and the operation of dropping and kneading is repeated to determine the amount of water at which the entire sample softens and starts to fluidize. , Calculated as the amount of water per 100 g of the sample. In other words, when the metal spatula is wound up into a spiral shape, when it is not wound up into a spiral shape, the water content immediately before it sticks to the glass plate is calculated by suddenly softening with one drop of distilled water. It is.

【0019】かかる範囲の吸水量を有することにより、
本発明において使用する結合剤は適度に練合する際の水
分を吸収することになる。これにより本発明のA成分で
あるアジ化化合物の水溶解を抑制でき、特に湿式押出造
粒時の固体相、液体相及び気体相の割合を成型に適した
割合に安定的に保持することが可能となった。吸水量が
200ml/100g未満では吸水量が不十分なため、
アジ化化合物の水溶解を抑制できず、1200ml/1
00gを越えると押出造粒時の可塑性が不足し造粒が困
難となるため好ましくない。
By having such a range of water absorption,
The binder used in the present invention absorbs moisture when kneading to an appropriate degree. This makes it possible to suppress the dissolution of the azide compound as the component A of the present invention in water, and particularly to stably maintain the proportions of the solid phase, the liquid phase and the gas phase during wet extrusion granulation to the proportions suitable for molding. It has become possible. If the water absorption is less than 200 ml / 100 g, the water absorption is insufficient,
Water dissolution of the azide compound could not be suppressed, 1200 ml / 1
If it exceeds 00 g, the plasticity at the time of extrusion granulation becomes insufficient and granulation becomes difficult, which is not preferable.

【0020】上記に示す結合剤の作用により、かかる結
合剤は練合水分に対して、上記に示す吸水性を有し、溶
解性が低く、更に粘性の高い状態となるものが好まし
い。
By the action of the above-mentioned binder, it is preferable that such a binder has the above-described water absorption to kneading water, has low solubility, and has a high viscosity.

【0021】かかる観点及び土壌処理剤に使用するとの
観点から、本発明のC成分として好ましい結合剤として
は、かかる吸水量範囲を満足するアルファー化された化
工デンプン、デキストリン、アラビアガム、カルボキシ
メチルセルロース、メチルセルロース、ヒドロキシプロ
ピルセルロース、ポリビニルアルコール、部分けん化酢
酸ビニル、ポリビニルピロリドン、カルボキシメチルセ
ルロースのアルカリ塩等が挙げられる。これらは単独で
用いてもよいし、目的とする粒度範囲、水面沈降あるい
は浮上、及び水中における崩壊あるいは非崩壊等の物理
化学的特性に合わせて2成分以上を混合して用いること
もできる。
From this viewpoint and from the viewpoint of use as a soil treatment agent, preferred binders as the C component of the present invention include pregelatinized modified starch, dextrin, gum arabic, carboxymethylcellulose, which satisfies such a water absorption range. Examples include methylcellulose, hydroxypropylcellulose, polyvinyl alcohol, partially saponified vinyl acetate, polyvinylpyrrolidone, and alkali salts of carboxymethylcellulose. These may be used alone, or two or more components may be mixed and used in accordance with the physicochemical properties such as a target particle size range, water surface sedimentation or floating, and disintegration or non-disintegration in water.

【0022】更に本発明のA成分であるアジ化化合物と
の相互作用の観点から、吸水量が200〜1200ml
/100gであるアルファー化されたデンプン及びカル
ボキシメチルセルロースのアルカリ塩、例えばカルボキ
シメチルセルロースナトリウムが特に好ましい。
Further, from the viewpoint of the interaction with the azide compound which is the component A of the present invention, the water absorption is 200 to 1200 ml.
Particularly preferred are pregelatinized starch and alkali salts of carboxymethylcellulose, for example sodium carboxymethylcellulose, which is / 100 g.

【0023】本発明におけるアジ化水素を発生しうるア
ジ化化合物(A成分)、増量剤(B成分)及び特定の吸
水量を有する結合剤(C成分)の混合比率としては、A
成分10〜70重量%、B成分30〜90重量%である
A成分とB成分の合計100重量部に対し、C成分が1
〜25重量部であり、かつA成分に対するC成分の重量
比が0.1〜1.0であるものが好ましい。更に好まし
くはA成分15〜60重量%、B成分が40〜85重量
%の合計100重量部に対し、C成分が2〜20重量部
であり、かつA成分に対するC成分の重量比が0.1〜
1.0であり、特に好ましくはC成分が3〜15重量部
であり、かつA成分とC成分の重量比が0.15〜0.
40の範囲内にあるものである。
In the present invention, the mixing ratio of the azide compound capable of generating hydrogen azide (component A), the extender (component B) and the binder having a specific water absorption (component C) is as follows.
Component C is added in an amount of 1 to 70% by weight of component A and 30 to 90% by weight of component B, and 100 parts by weight of component A and component B in total.
It is preferable that the weight ratio of the C component to the A component is 0.1 to 1.0 part by weight. More preferably, the C component is 2 to 20 parts by weight, and the weight ratio of the C component to the A component is 0.1 to 100 parts by weight, which is 15 to 60% by weight of the A component and 40 to 85% by weight of the B component. 1 to
1.0, particularly preferably the C component is 3 to 15 parts by weight, and the weight ratio of the A component to the C component is 0.15 to 0.1.
It is in the range of 40.

【0024】A成分とB成分の合計100重量部中A成
分が10重量%未満では、薬効が十分でなく、一方70
重量%を越えると粒剤を製造することが極めて困難とな
り好ましくない。一方C成分が1重量部未満では結合剤
の量が不十分なため、25重量部を越える場合には組成
物の可塑性が不足し、押出造粒が困難となり好ましくな
い。更にA成分に対するC成分の重量比が0.1未満の
場合には、A成分の水溶解を十分に抑制できないため粒
剤の成型が困難となり、重量比が1.0を越える場合に
は組成物の可塑性が不足し、押出造粒が困難となり好ま
しくない。
If the amount of the component A is less than 10% by weight in the total of 100 parts by weight of the components A and B, the efficacy is not sufficient.
Exceeding the weight percentage makes it extremely difficult to produce granules, which is not preferred. On the other hand, if the amount of the component C is less than 1 part by weight, the amount of the binder is insufficient. If the amount exceeds 25 parts by weight, the plasticity of the composition becomes insufficient and extrusion granulation becomes difficult, which is not preferable. Further, when the weight ratio of the component C to the component A is less than 0.1, the dissolution of the component A in water cannot be sufficiently suppressed, so that the molding of the granules becomes difficult. The plasticity of the product is insufficient, and extrusion granulation becomes difficult, which is not preferable.

【0025】本発明の生物防除用粒状土壌処理剤にはA
成分、B成分、及びC成分以外にも、本発明の目的を損
なわない範囲で、すなわち本発明の製剤工程や粒剤品質
に大きな影響を与えない範囲で、必要に応じて種々の物
質を添加することができる。例えば、土壌処理剤を散布
する際に、土壌表層の散布状態の均一性を容易に識別確
認する目的で、染料あるいは顔料成分を添加して、本発
明の粒状土壌処理剤を着色することができる。その添加
方法にはA成分、B成分、及びC成分と同時に着色剤を
混合し、その後蒸留水等の練合水を混合する方法の他、
水溶性染料であるならばその必要量をあらかじめ練合水
に溶解しておき、その着色練合水を加えてもよい。
The granular soil treating agent for biocontrol of the present invention includes A
In addition to the components, B component and C component, various substances are added as needed within a range that does not impair the purpose of the present invention, that is, within a range that does not greatly affect the preparation process and granule quality of the present invention. can do. For example, when spraying a soil treating agent, a dye or pigment component can be added to color the granular soil treating agent of the present invention by adding a dye or pigment component for the purpose of easily identifying and confirming the uniformity of the applied state of the soil surface layer. . In addition to the method of adding the colorant simultaneously with the A component, the B component, and the C component, and then kneading water such as distilled water,
If it is a water-soluble dye, its necessary amount may be dissolved in kneading water in advance, and the coloring kneading water may be added.

【0026】また本発明の生物防除用粒状土壌処理剤か
ら、有効成分であるアジ化化合物の放出を制御する目的
で、かかる土壌処理剤にさらなる補助剤を添加すること
も可能である。すなわち、有効成分であるアジ化化合物
は土壌中に含まれる水分と接触して、溶解及びガス化の
反応が進むことから、これら水分との接触を促進あるい
は均質化する目的で、ラウリル硫酸ナトリウム等の陰イ
オン界面活性剤や、ポリオキシエチレンノニルフェニル
エーテル等の非イオン界面活性剤を添加してもよい。ま
た、反対に作業性の問題等でガス化を遅延したい場合に
は水分との接触を疎外あるいは排除する目的で、ステア
リン酸カルシウム等の金属石鹸類、あるいはシリコンオ
イル等の撥水剤を必要に応じた適当量を添加してもよ
い。
Further, for the purpose of controlling the release of an azide compound as an active ingredient from the granular soil treating agent for biological control of the present invention, it is possible to add a further auxiliary agent to the soil treating agent. In other words, the azide compound, which is an active ingredient, comes into contact with moisture contained in soil, and the dissolution and gasification reactions proceed. Therefore, sodium lauryl sulfate or the like is used for the purpose of promoting or homogenizing the contact with such moisture. May be added, or a nonionic surfactant such as polyoxyethylene nonylphenyl ether may be added. Conversely, if it is desired to delay gasification due to workability problems, etc., use a metal soap such as calcium stearate or a water repellent such as silicone oil as necessary for the purpose of eliminating or eliminating contact with moisture. Alternatively, an appropriate amount may be added.

【0027】また、本発明の生物防除用粒状土壌処理剤
には、さらなる土壌処理消毒剤の効果を補強する目的
で、すでに公知の農薬有効成分をその必要に応じて添加
することも可能である。例えば、土壌中の殺線虫効果を
増強及び拡大する目的で、アジ化化合物に加えて殺線虫
効果の高いホスチアゼート(ブチル−O−エチル−2−
オキソ−1,3−チアゾリジン−3−イルホスホノチオ
アト)を本発明の粒状土壌処理剤に添加することも可能
である。また、同様に土壌殺菌効果を補強及び拡大する
目的でアジ化化合物に加えて汎用殺菌効果の高い微粉化
されたTPN(テトラクロロイソフタロニトリル)を本
発明の粒状土壌処理剤に加えることもできる。さらに同
様に、雑草の除草効果を増強及び拡大する目的で、アジ
化化合物に加えて畑地除草効果の高いDCMU(3−
(3,4−ジクロロフェニル) −1,1ジメチル尿素)
を本発明の土壌処理剤に加えて粒状化することも可能で
ある。
In order to reinforce the effect of the disinfectant for soil treatment, known active ingredients for agricultural chemicals can be added to the granular soil treatment agent for biological control of the present invention, if necessary. . For example, in order to enhance and expand the nematicidal effect in soil, in addition to the azide compound, phosthiazate (butyl-O-ethyl-2-yl) having a high nematicidal effect is added.
Oxo-1,3-thiazolidin-3-ylphosphonothioato) can also be added to the granular soil treating agent of the present invention. Similarly, in addition to an azide compound, micronized TPN (tetrachloroisophthalonitrile) having a high general bactericidal effect can be added to the granular soil treating agent of the present invention in addition to the azide compound for the purpose of reinforcing and expanding the soil bactericidal effect. . Similarly, in order to enhance and expand the weed herbicidal effect of weeds, in addition to azide compounds, DCMU (3-
(3,4-dichlorophenyl) -1,1 dimethyl urea)
Can be added to the soil treating agent of the present invention to form granules.

【0028】本発明の生物防除用粒状土壌処理剤の製法
としては、例えば本発明のA成分、B成分、C成分、及
びその他の添加物の混合物に更に水を加えて練り合わせ
た後、押出成型又は圧縮成型して造粒し、これを乾燥し
て水分を除去する方法を用いることができる。造粒方法
としては特に湿式押出造粒法が簡便かつ効率的な造粒法
として好ましく、本発明の組成物は特にかかる造粒法に
適したものである。
The method for producing the granular soil treating agent for biological control according to the present invention includes, for example, kneading a mixture of the component A, component B, and component C of the present invention with additional water, followed by extrusion molding. Alternatively, a method of compressing and granulating, drying this and removing moisture can be used. As a granulation method, a wet extrusion granulation method is particularly preferred as a simple and efficient granulation method, and the composition of the present invention is particularly suitable for such a granulation method.

【0029】より具体的には、練合された組成物を目的
とするサイズに適した孔径を有する押出ダイスあるいは
スクリーンを選択することにより、取り扱い性に優れた
粒径サイズの粒剤を容易に作ることができる。押出造粒
法にはスクリュー型(横型あるいは前押し型ともいう)
あるいは円筒型(縦型ともいう)等の各種方式がある
が、いずれの型式においても本発明の組成物は適してお
り、目的とする粒剤を効率よく得ることができる。
More specifically, by selecting an extrusion die or screen having a pore size suitable for the size of the kneaded composition, granules having a particle size excellent in handleability can be easily prepared. Can be made. Screw type (also called horizontal type or pre-press type) for extrusion granulation
Alternatively, there are various types such as a cylindrical type (also referred to as a vertical type). In any of the types, the composition of the present invention is suitable, and a target granule can be obtained efficiently.

【0030】[0030]

【発明の実施の形態】以下に実施例を挙げて更に説明す
る。なお実施例中の部は重量部であり、%は重量%を示
す。吸水量の測定方法及び造粒収率の評価方法を下記に
示す。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be further described below with reference to examples. Parts in Examples are parts by weight, and% indicates% by weight. The method for measuring the water absorption and the method for evaluating the granulation yield are shown below.

【0031】1.吸水量の測定方法 JIS K−5101に規定する「吸油量の測定方法」
の測定条件に準じて以下の要領で測定を行った。23
℃、相対湿度50%の雰囲気下、本発明のC成分である
結合剤の試料粉末10gを200ml容のガラスビーカ
ーに入れ、これにビュレットを用いて蒸留水を0.5m
lずつ程度を目安に静かに滴下する。滴下の都度金属へ
らで十分に練り合わせ、試料粉末との均質化を図る。滴
下及び練り合わせの操作を繰り返し、試料全体が軟化
し、流動化し始める水分量(Aml)、すなわち金属ヘ
ラでラセン形に巻き起こされる程度になった時の水分量
を求め、次式により計算する。但し流動化の開始は、注
水終了の1分後の状態で判定する。 吸水量(ml/100g) = A × 10
1. Method of measuring water absorption "Method of measuring oil absorption" specified in JIS K-5101
The measurement was performed in the following manner according to the measurement conditions described in above. 23
In an atmosphere of 50 ° C. and a relative humidity of 50%, 10 g of a sample powder of the binder as the component C of the present invention was placed in a 200 ml glass beaker, and 0.5 ml of distilled water was added thereto using a burette.
Gently add the solution gently at a rate of 1 l. Each time it is dropped, it is thoroughly kneaded with a metal spatula to achieve homogenization with the sample powder. The operation of dropping and kneading is repeated to obtain the amount of water (Aml) at which the whole sample starts to soften and fluidize, that is, the amount of water when the metal spatula is formed into a spiral shape, and is calculated by the following equation. However, the start of fluidization is determined in a state one minute after the end of water injection. Water absorption (ml / 100g) = A x 10

【0032】2.造粒品収率の評価方法 以下の実施例及び比較例で得られた造粒品、すなわち押
出造粒後の造粒物をそのまま乾燥したものを、48メッ
シュ(300μm)及び9メッシュ(2000μm)で
篩い分け、全粒子中における48〜9メッシュの粒状物
の比率を算出し、造粒品収率として表わした。この値が
高いほど製品に近い造粒物が得られているため、そのま
まの状態で整粒工程にかけられ、且つ均質な形状のもの
を得ることができる。
2. Evaluation method of granulated product yield Granulated products obtained in the following Examples and Comparative Examples, that is, those obtained by drying granules after extrusion granulation as they are, were subjected to 48 mesh (300 μm) and 9 mesh (2000 μm) meshes. And the ratio of the 48 to 9 mesh granular material in all the particles was calculated and expressed as the yield of granulated product. As this value is higher, a granulated product closer to the product is obtained, so that the granulated product can be subjected to a sizing process as it is and a product having a uniform shape can be obtained.

【0033】3.製品収率の評価方法 以下の実施例及び比較例で得られた製品、すなわち押出
造粒後の造粒物を、整粒工程を経て整粒したのち、かか
る粒剤を乾燥したものを48メッシュ(300μm)及
び16メッシュ(1000μm)で篩い分け、全粒子中
における48〜16メッシュの粒状物の比率を算出し、
製品収率として表わした。かかる粒径範囲は農薬取締法
に基づく粒剤の粒径範囲、すなわち48メッシュ〜10
メッシュ(300μm〜1700μm)の範囲に入るも
のとなる。すなわち、かかる製品収率が高いものほど製
造効率に優れるものとなる。
3. Product Yield Evaluation Method The product obtained in the following Examples and Comparative Examples, that is, the granulated product after extrusion granulation, after sieving through a sizing step, dried such granules were 48 mesh (300 μm) and 16 mesh (1000 μm), and calculate the ratio of the granular material of 48 to 16 mesh in all the particles,
Expressed as product yield. Such a particle size range is a particle size range of granules based on the Agricultural Chemicals Control Law, that is, 48 mesh to 10 mesh.
It falls within the range of mesh (300 μm to 1700 μm). That is, the higher the product yield, the higher the production efficiency.

【0034】[実施例1]80メッシュ以下であるアジ
化ナトリウム粉末(東洋化成(株)製)750部を、ク
レー(勝光山鉱業所(株)製、Aクレー)1971部に
加えよく混和した。更にステアリン酸カルシウム90部
(和光純薬(株)製)及びアルファー化した化工デンプ
ン150部(日澱化学(株)製、アミコールC)、ホワ
イトカーボン30部(日本シリカ(株)製、ニプシール
NS)を加え混和した後、これをニーダー(不二パウダ
ル(株)製、DHJ−10型)に入れ、あらかじめ蒸留
水491重量部に水酸化ナトリウム9部を溶解した練合
水500部を常温条件下、徐々に注水して均一物になる
まで捏和した。ついでかかる捏和物を孔径0.8mmの
ドーム型ダイのスクリーンを付けた押出造粒機(不二パ
ウダル(株)製、DG−L1型)を使用し常温下で造粒
の後、流動層乾燥機(不二パウダル(株)製、2F型)
で80℃にて練合水分を蒸発させ、アジ化ナトリウムを
25%含有する造粒品3000部を得た。一方同様の組
成及び条件にて造粒後、かかる造粒物をそのまま整粒機
に投入して整粒し、その後流動層乾燥機(不二パウダル
(株)製、2F型)で80℃にて乾燥し製品3000部
を得た。
[Example 1] 750 parts of sodium azide powder (manufactured by Toyo Kasei Co., Ltd.) having a mesh size of 80 mesh or less was added to 1971 parts of clay (manufactured by Katsumitsu Mine Co., Ltd., A clay) and mixed well. . Furthermore, 90 parts of calcium stearate (manufactured by Wako Pure Chemical Industries, Ltd.) and 150 parts of pregelatinized modified starch (manufactured by Nichien Chemical Co., Ltd., AMICOL C), 30 parts of white carbon (manufactured by Nippon Silica Co., Ltd., Nipsil NS) Was added and mixed, and the mixture was placed in a kneader (Model DHJ-10, manufactured by Fuji Paudal Co., Ltd.), and 500 parts of kneaded water in which 9 parts of sodium hydroxide was previously dissolved in 491 parts by weight of distilled water were added at room temperature. Then, water was gradually added and kneaded until a uniform product was obtained. Then, the kneaded product is granulated at room temperature using an extrusion granulator (DG-L1 type, manufactured by Fuji Paudal Co., Ltd.) equipped with a screen of a dome-shaped die having a pore diameter of 0.8 mm. Dryer (2F type, manufactured by Fuji Paudal Co., Ltd.)
The kneading water was evaporated at 80 ° C. to obtain 3000 parts of a granulated product containing 25% of sodium azide. On the other hand, after granulation under the same composition and conditions, the granulated product is directly charged into a granulator and sized, and then heated to 80 ° C. with a fluid bed dryer (2F type, manufactured by Fuji Paudal Co., Ltd.). And dried to obtain 3000 parts of the product.

【0035】[実施例2]80メッシュ以下であるアジ
化ナトリウム粉末(東洋化成(株)製)1000部を、
クレー(勝光山鉱業所(株)製、Aクレー)774部に
加えよく混和した。更にアルファー化した化工デンプン
200部(三和澱粉(株)製、コーンアルファY)、ホ
ワイトカーボン20部((株)トクヤマ製、トクシール
GUN)を加え混和した後、これをニーダー(不二パウ
ダル(株)製、DHJ−10型)に入れ、あらかじめ蒸
留水234部に水酸化ナトリウム6部を溶解した練合水
240部を徐々に注水して常温下で均一になるまで捏和
した。ついでこの捏和物を常温下孔径1.2mmのドー
ム型ダイのスクリーンを付けた押出造粒機(不二パウダ
ル(株)製DG−L1型)で粗造粒の後、引き続き孔径
0.6mmのスクリーンで造粒した。その後、これら造
粒物を流動層乾燥機(不二パウダル(株)製、2F型)
で80℃にて含有水分を蒸発除去し、アジ化ナトリウム
を50%含有する造粒品2000部を得た。一方同様の
組成及び条件にて造粒後、上記実施例1と同様に整粒及
び乾燥して製品2000部を得た。
Example 2 1000 parts of sodium azide powder (manufactured by Toyo Kasei Co., Ltd.) having a mesh size of 80 mesh or less
It was added to 774 parts of clay (Aclay manufactured by Katsumitsu Mining Co., Ltd.) and mixed well. Further, 200 parts of pregelatinized modified starch (manufactured by Sanwa Starch Co., Ltd., Corn Alpha Y) and 20 parts of white carbon (manufactured by Tokuyama Co., Ltd., Tokusil GUN) were added and mixed. Co., Ltd., DHJ-10 type), 240 parts of kneaded water in which 6 parts of sodium hydroxide were previously dissolved in 234 parts of distilled water were gradually poured, and kneaded at room temperature until uniform. Then, the kneaded product was coarsely granulated at room temperature by an extrusion granulator (DG-L1 type, manufactured by Fuji Paudal Co., Ltd.) equipped with a dome-shaped die screen having a hole diameter of 1.2 mm, and then the hole diameter was continuously 0.6 mm. Granulated with a screen. Then, these granulated products are fluidized bed dryers (2F type, manufactured by Fuji Paudal Co., Ltd.)
The water content was removed by evaporation at 80 ° C. to obtain 2,000 parts of a granulated product containing 50% of sodium azide. On the other hand, after granulation under the same composition and conditions, the mixture was sized and dried in the same manner as in Example 1 to obtain 2000 parts of a product.

【0036】[実施例3]80メッシュ以下に微粉化さ
れたアジ化ナトリウム粉末(東洋化成(株)製)564
部に、クレー(勝光山鉱業所(株)製、Aクレー)22
77部を加えてよく混和した。さらにポリビニルアルコ
ール120部(日本合成(株)製、ゴーセノールGL−
05S)、およびホワイトカーボン30部((株)トク
ヤマ製、トクシールGUN)を加えた後、これらの全量
をニーダー(不二パウダル(株)製、DHJ−10型)
に投入し、あらかじめ水酸化ナトリウム9部を蒸留水3
65部に溶解した練合水374部を徐々に注水して常温
下で均一になるまで捏和した。均一に湿潤したこの捏和
物を、常温下孔径0.8mmのドームダイ式のスクリー
ンをもつ押出造粒機(不二パウダル(株)製、DG−L
1型)で造粒した。その後、これら造粒物を流動層乾燥
機(不二パウダル(株)製、2F型)で80℃にて含有
水分を蒸発除去し、アジ化ナトリウムを18.8%含有
する造粒品3000部を得た。一方同様の組成及び条件
にて造粒後、上記実施例1と同様に整粒及び乾燥して製
品3000部を得た。
[Example 3] Sodium azide powder (Toyo Kasei Co., Ltd.) pulverized to 80 mesh or less 564
Clay (Atsu clay manufactured by Katsumitsu Mining Co., Ltd.) 22
77 parts were added and mixed well. Further, 120 parts of polyvinyl alcohol (Gosenol GL- manufactured by Nippon Gosei Co., Ltd.)
05S), and 30 parts of white carbon (Tokusyl GUN, manufactured by Tokuyama Corporation), and then the entire amount thereof was kneaded (Model DHJ-10, manufactured by Fuji Paudal Co., Ltd.).
And 9 parts of sodium hydroxide beforehand in distilled water 3
374 parts of kneaded water dissolved in 65 parts were gradually poured, and kneaded at room temperature until uniform. The kneaded product uniformly moistened was subjected to an extrusion granulator (DG-L, manufactured by Fuji Paudal Co., Ltd.) having a dome die type screen having a hole diameter of 0.8 mm at room temperature.
(Type 1). Thereafter, the water content of these granules was removed by evaporation at 80 ° C. using a fluid bed dryer (2F type, manufactured by Fuji Paudal Co., Ltd.), and 3000 parts of granules containing 18.8% of sodium azide were removed. I got On the other hand, after granulation under the same composition and conditions, the mixture was sized and dried in the same manner as in Example 1 to obtain 3000 parts of a product.

【0037】[実施例4]実施例3と同様に製造する
際、ポリビニルアルコール120部に替えてカルボキシ
メチルセルロースナトリウム120部(第一工業製薬
(株)製、セロゲン7A)を用い、以下同様に操作して
アジ化ナトリウムを18.8%含有する造粒物3000
部及び製品3000部を得た。
Example 4 In the same manner as in Example 3, except that 120 parts of polyvinyl alcohol was replaced with 120 parts of sodium carboxymethylcellulose (Cellogen 7A, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.), and the same procedure was followed. To give granules containing 18.8% sodium azide
Parts and 3000 parts of product.

【0038】[比較例1]あらかじめ80メッシュ以下
に微粉化したアジ化ナトリウム粉末(東洋化成(株)
製)566部を、タルク(日本タルク(株)製、SW
B)2284部に加え混合する。さらに乳鉢で60メッ
シュ以下に粉砕したポリエチレングリコール6000
(和光純薬(株)製、試薬)粉末の150部を、あらか
じめ加温した練合水330部と混和して均一な糊状の液
を調製する。粉末混合物の全量をニーダー(不二パウダ
ル(株)製、DHJ−10型)に入れて、上部よりこの
調製液の全量を添加しつつ常温下で捏和した。目視によ
り捏和物の外観が均一になるまで捏和し、かかる捏和物
を孔径0.8mmのドーム型ダイのスクリーンを付けた
押出造粒機(不二パウダル(株)製DG−L1型)を使
用し常温下で造粒した。かかる造粒物の全量を流動層乾
燥機(不二パウダル(株)製、2F型)に入れ、80℃
にて捏和に用いた水分を蒸発、留去し、アジ化ナトリウ
ムを18.8%含有する造粒品3000部を得た。一方
同様の組成及び条件にて造粒後、上記実施例1と同様に
整粒及び乾燥して製品3000部を得た。但し得られた
製品は実施例1〜4に比較して製品である粒剤個々にお
いて割れや欠けが目立ち、形状が不均一であった。
[Comparative Example 1] A sodium azide powder previously finely ground to 80 mesh or less (Toyo Kasei Co., Ltd.)
566 parts of talc (manufactured by Nippon Talc Co., Ltd., SW
B) Add to 2284 parts and mix. In addition, polyethylene glycol 6000 ground to 60 mesh or less in a mortar
(Reagent, manufactured by Wako Pure Chemical Industries, Ltd.) 150 parts of powder is mixed with 330 parts of kneaded water that has been heated in advance to prepare a uniform paste-like liquid. The whole amount of the powder mixture was put into a kneader (Model DHJ-10, manufactured by Fuji Paudal Co., Ltd.), and kneaded at room temperature while adding the whole amount of the prepared solution from above. The kneaded product was kneaded with the naked eye until the appearance of the kneaded product became uniform, and the kneaded product was extruded with a dome-shaped die screen having a hole diameter of 0.8 mm (DG-L1 manufactured by Fuji Paudal Co., Ltd.). ) And granulated at room temperature. The whole amount of the granulated product was put into a fluid bed dryer (2F type, manufactured by Fuji Paudal Co., Ltd.),
The water used for kneading was evaporated and distilled off to obtain 3000 parts of a granulated product containing 18.8% of sodium azide. On the other hand, after granulation under the same composition and conditions, the mixture was sized and dried in the same manner as in Example 1 to obtain 3000 parts of a product. However, in the obtained product, as compared to Examples 1 to 4, cracks and chips were conspicuous in each of the product granules, and the shape was uneven.

【0039】[比較例2]比較例1と同様に製造する
際、整粒機にかける前に造粒物をある程度細かくなるま
で手でほぐし、その後整粒機に投入することにより整粒
したこと以外は比較例1と同様に行い、製品を得た。但
し得られた製品は実施例1〜4に比較して製品である粒
剤個々において割れや欠けが目立ち、形状が不均一であ
った。
[Comparative Example 2] In the same manner as in Comparative Example 1, before granulation, the granulated product was loosened by hand until it became fine to some extent, and then the granulated product was sieved by being put into a granulator. A product was obtained in the same manner as in Comparative Example 1 except for the above. However, in the obtained product, as compared to Examples 1 to 4, cracks and chips were conspicuous in each of the product granules, and the shape was uneven.

【0040】[比較例3]比較例1と同様に製造する
際、糊状の液を調製する工程を経ず、ポリエチレングリ
コール6000(和光純薬(株)製、試薬)を60メッ
シュ以下に粉砕した粉末状態で他の粉末原料と混合の
後、ニーダーにて常温下練合水330部を徐々に添加し
ながら均一になるまで捏和した。かかる捏和物を孔径
0.8mmのドーム型ダイのスクリーンを付けた押出造
粒機(不二パウダル(株)製DG−L1型)を使用し常
温下で造粒することを試みたが、練合物の弾性が不足し
スクリーン通過後の形状を保つことができず、造粒する
ことができなかった。実施例および比較例に用いた結合
剤の吸水量と、造粒収率との関係を表1の比較表にまと
めた。
Comparative Example 3 In the same manner as in Comparative Example 1, polyethylene glycol 6000 (a reagent manufactured by Wako Pure Chemical Industries, Ltd.) was pulverized to 60 mesh or less without the step of preparing a paste-like liquid. After mixing with the other powder raw materials in the powdered state, the mixture was kneaded with a kneader at room temperature while gradually adding 330 parts of kneaded water until the mixture became uniform. An attempt was made to granulate the kneaded product at room temperature by using an extrusion granulator (DG-L1 manufactured by Fuji Paudal Co., Ltd.) equipped with a screen of a dome-shaped die having a hole diameter of 0.8 mm. The elasticity of the kneaded product was insufficient and the shape after passing through the screen could not be maintained, and granulation could not be performed. The relationship between the water absorption of the binder used in the examples and the comparative examples and the granulation yield is summarized in the comparative table of Table 1.

【0041】[0041]

【表1】 [Table 1]

【0042】この表から明らかなように、吸水量が特定
の範囲にある場合には目的とする粒剤を高収率で得るこ
とが可能であることがわかる。一方吸水量が範囲外の場
合には、比較例1及び2に示すように一旦結合剤を水に
溶解する工程や、整粒工程前に手でほぐす等の煩雑な工
程を必要とし生産性が低い上、更に形状の不均一さがあ
り商品価値としては劣るものとなる。また手でほぐすな
どの工程を経ない場合には製品収率が低下する。更に比
較例3に示すように実施例1〜4と同様に水のみを別途
添加する場合には、粒剤が製造できないことがわかる。
As is clear from this table, when the amount of water absorption is in a specific range, it is possible to obtain the target granule in a high yield. On the other hand, when the water absorption is out of the range, as shown in Comparative Examples 1 and 2, a step of once dissolving the binder in water or a complicated step of loosening by hand before the sizing step is required, and the productivity is reduced. In addition to being low, there is further unevenness in the shape, resulting in poor commercial value. In addition, if the process such as loosening by hand is not performed, the product yield decreases. Furthermore, as shown in Comparative Example 3, when only water is separately added similarly to Examples 1 to 4, it can be seen that granules cannot be produced.

【0043】[0043]

【発明の効果】本発明の生物防除用粒状土壌処理剤は、
アジ化化合物を高充填で含有しかつ目的とする適正な粒
径の製品を効率的に製造でき、農薬としての商品価値の
高い生物防除用粒状土壌処理剤を提供できることから、
その奏する工業的効果は格別なものである。
The granular soil treating agent for biological control of the present invention comprises:
Since it is possible to efficiently produce a product having an appropriate particle size and containing an azide compound at a high loading and to provide a granular soil treatment agent for biological control having a high commercial value as an agricultural chemical,
The industrial effects they produce are exceptional.

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 分解によりアジ化水素を発生し得るアジ
化化合物(A成分)、増量剤(B成分)、及び吸水量が
200〜1200ml/100gである結合剤(C成
分)からなる生物防除用粒状土壌処理剤。
1. Biological control comprising an azide compound capable of generating hydrogen azide by decomposition (component A), a bulking agent (component B), and a binder (component C) having a water absorption of 200 to 1200 ml / 100 g. For granular soil treatment agent.
【請求項2】 C成分がアルファー化された化工デンプ
ン及び/又はカルボキシメチルセルロースのアルカリ塩
である請求項1に記載の生物防除用粒状土壌処理剤。
2. The granular soil treating agent for biological control according to claim 1, wherein the C component is a pregelatinized modified starch and / or an alkali salt of carboxymethylcellulose.
【請求項3】 B成分がタルク、パイロフィライト系ろ
う石クレー、ジークライト、炭酸カルシウム、消石灰か
ら選択される少なくとも1種からなる請求項1又は2の
いずれか1項に記載の生物防除用粒状土壌処理剤。
3. The biocontrol agent according to claim 1, wherein the B component comprises at least one selected from talc, pyrophyllite-based pyroxene clay, ziglite, calcium carbonate, and slaked lime. Granular soil treatment agent.
【請求項4】 A成分、B成分及びC成分からなる生物
防除用粒状土壌処理剤において、A成分が10〜70重
量%、B成分が30〜90重量%であり、A成分とB成
分の合計100重量部に対して、C成分が1〜25重量
部であり、かつA成分に対するC成分の重量比が0.1
〜1.0である請求項1〜3のいずれか1項に記載の生
物防除用粒状土壌処理剤。
4. A granular soil treatment agent for biological control comprising A component, B component and C component, wherein the A component is 10 to 70% by weight, the B component is 30 to 90% by weight, and the A component and the B component The C component is 1 to 25 parts by weight with respect to 100 parts by weight in total, and the weight ratio of the C component to the A component is 0.1.
The granular soil treating agent for biological control according to any one of claims 1 to 3, which is 1.0 to 1.0.
【請求項5】 A成分が15〜60重量%、B成分が4
0〜85重量%であり、A成分とB成分の合計100重
量部に対して、C成分が3〜15重量部であり、かつA
成分に対するC成分の重量比が0.15〜0.40であ
ることを特徴とする請求項4に記載の生物防除用粒状土
壌処理剤。
5. Component A is 15 to 60% by weight, and Component B is 4% by weight.
0 to 85% by weight, and 3 to 15 parts by weight of the component C with respect to 100 parts by weight of the total of the component A and the component B;
The granular soil treating agent for biological control according to claim 4, wherein the weight ratio of the component C to the component is 0.15 to 0.40.
JP378598A 1998-01-12 1998-01-12 Granular soil treatment agent for controlling organism Withdrawn JPH11199416A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP378598A JPH11199416A (en) 1998-01-12 1998-01-12 Granular soil treatment agent for controlling organism

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP378598A JPH11199416A (en) 1998-01-12 1998-01-12 Granular soil treatment agent for controlling organism

Publications (1)

Publication Number Publication Date
JPH11199416A true JPH11199416A (en) 1999-07-27

Family

ID=11566847

Family Applications (1)

Application Number Title Priority Date Filing Date
JP378598A Withdrawn JPH11199416A (en) 1998-01-12 1998-01-12 Granular soil treatment agent for controlling organism

Country Status (1)

Country Link
JP (1) JPH11199416A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6852341B2 (en) 2000-10-10 2005-02-08 Auburn University Azide method and composition for controlling deleterious organisms and for stimulating beneficial organisms
US6932985B2 (en) 2000-10-10 2005-08-23 Auburn University Azide method and composition for controlling deleterious organisms
WO2019050192A1 (en) * 2017-09-08 2019-03-14 주식회사 경농 Soil moisturizing and binding composition and preparation method therefor
JP2019156836A (en) * 2018-03-09 2019-09-19 三井化学アグロ株式会社 Agricultural and horticultural granular composition and method for producing said composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6852341B2 (en) 2000-10-10 2005-02-08 Auburn University Azide method and composition for controlling deleterious organisms and for stimulating beneficial organisms
US6932985B2 (en) 2000-10-10 2005-08-23 Auburn University Azide method and composition for controlling deleterious organisms
WO2019050192A1 (en) * 2017-09-08 2019-03-14 주식회사 경농 Soil moisturizing and binding composition and preparation method therefor
JP2019156836A (en) * 2018-03-09 2019-09-19 三井化学アグロ株式会社 Agricultural and horticultural granular composition and method for producing said composition

Similar Documents

Publication Publication Date Title
JP3420591B2 (en) Dispersible granules for disinfecting and fungicidal products
JPH06336403A (en) Divided spreadable solid agrochemical preparation packaged in water-soluble paper
US3980463A (en) Process for producing granular composition for use in agriculture and horticulture
EP1488697B1 (en) Granulated wettable powder
JPH11199416A (en) Granular soil treatment agent for controlling organism
JPS58133827A (en) Water dispersible or soluble particle, production and use thereof
JPH0240301A (en) Agricultural and horticultural granular wettable powder and production thereof
JP4919662B2 (en) Uniform diffusible granular pesticide formulation
ES2202037T3 (en) PROCEDURE TO PRODUCE GRANULES.
JP5207262B2 (en) Granular wettable powder
JPH10158111A (en) Stabilized agrochemical solid preparation
JP3645920B2 (en) Water-soluble pesticide granules
JPH0517302A (en) Granular substance and its production
JP4421309B2 (en) Agricultural and horticultural granule wettable powder
CN105248445A (en) Slow-release thiamethoxam water dispersible granule and preparing method thereof
JPH10109904A (en) Granular herbicide for rice paddies
RU2147179C1 (en) Dosed pesticidal agent in the form of single pressed mold
JP2932077B2 (en) Pesticidal granular composition in which caking has been prevented
JP3869491B2 (en) Agrochemical granules
JPH06211610A (en) Herbicidal composition and tablet for paddy field
JP2003183106A (en) Water-surface-buoyant agrochemical preparation
JPH09255504A (en) Agrochemical solid formulation
JPH09110605A (en) Herbicidal granular preparation having controlled elution and its production
JP2001294501A (en) Wettable powder for agrochemical
JP2001288004A (en) Method for producing granular agrochemical composition

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20041012

A761 Written withdrawal of application

Effective date: 20061110

Free format text: JAPANESE INTERMEDIATE CODE: A761