JPH0429904A - Plant growth-promotive preparation - Google Patents
Plant growth-promotive preparationInfo
- Publication number
- JPH0429904A JPH0429904A JP13253890A JP13253890A JPH0429904A JP H0429904 A JPH0429904 A JP H0429904A JP 13253890 A JP13253890 A JP 13253890A JP 13253890 A JP13253890 A JP 13253890A JP H0429904 A JPH0429904 A JP H0429904A
- Authority
- JP
- Japan
- Prior art keywords
- dcip
- preparation
- core material
- microencapsulation
- plant growth
- 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
Links
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、植物生育促進としての効果を有するが、その
反面揮散速度が速い故に植物生育促進剤としての安定し
た使用が困難であるジクロルジイソプロピルエーテル(
以下DCIPと略す。)を、その揮散速度を調節して生
育促進剤として利用し易くしたカプセル化剤に関するも
のである。Detailed Description of the Invention [Industrial Application Field] The present invention is directed to dichlor, which has the effect of promoting plant growth, but has a high volatilization rate and therefore is difficult to stably use as a plant growth promoter. Diisopropyl ether (
Hereinafter abbreviated as DCIP. ) can be easily used as a growth promoter by adjusting its volatilization rate.
従来、有効成分であるDCIPは殺線虫成分として高い
活性を有することから国内で殺線虫剤として実用に供せ
られてきた。又同時にDCIPは植物に対する生育促進
効果もしばしば認められることか知られていた。しかし
ながらDCIPの蒸気圧は0.58mmHg/ 20℃
と比較的高いため、有効成分の消失か速く、生育促進効
果としては長期持続性に劣るという欠点があり、この欠
点をなくして薬効持続性を安定化させることが切望され
ているのが現状である。Conventionally, the active ingredient DCIP has been put into practical use as a nematocide in Japan because it has high activity as a nematocidal ingredient. At the same time, it was known that DCIP often has a growth promoting effect on plants. However, the vapor pressure of DCIP is 0.58 mmHg/20℃
Because the drug has a relatively high level of drug efficacy, its active ingredients disappear quickly and its growth promoting effect is not long-lasting.There is currently a strong desire to eliminate these drawbacks and stabilize the durability of the drug's efficacy. be.
さらに乳剤、又は無機鉱物、界面活性剤との練り込み、
含浸等によって得られる、水和剤、粒剤等の一般的な製
剤形態では揮散速度の制御が難しく実用上不可能である
。Furthermore, emulsion or kneading with inorganic minerals and surfactants,
In general formulations such as wettable powders and granules obtained by impregnation, controlling the volatilization rate is difficult and practically impossible.
一方、生育促進剤としての活性成分をマイクロカプセル
化することにより、その作用を徐放化して効力の持続性
を図るとともに対象以外の生物に対する悪影響を防止し
ようとすることが考えられる。現在迄、活性成分である
DCIPをそのまま芯材としてカプセル化する手法は何
ら開示されていない。On the other hand, by microcapsulating the active ingredient as a growth promoter, it is possible to release its action in a sustained manner to maintain its efficacy and to prevent adverse effects on organisms other than the target. Until now, no method has been disclosed for encapsulating the active ingredient DCIP as it is as a core material.
本発明の目的は、各種の環境下に応じて最適な揮発速度
を自由に調節できるマイクロカプセル壁を有し、長期間
に亘って植物の生育促進効果を有するDCIP内包徐放
性マイクロカプセル化製剤の提供にある。The object of the present invention is to provide a sustained-release microencapsulated preparation containing DCIP, which has a microcapsule wall that can freely adjust the optimum volatilization rate according to various environments, and has a long-term plant growth promoting effect. It is provided by.
本発明におけるDCIPのマイクロカプセル化において
は、DCIPの単独もしくはDCIPを含む混合物を芯
物質とし、DCIPの揮発速度の調整が可能な徐放性を
有する外壁材であって、しかもその薬効を低下させるこ
とのない外壁月1こよりDCIPをマイクロカプセル化
する方法を用いている。マイクロカプセル生成技術にお
いては広く公知の界面重合法、in −5iLu法、相
分離法、液中硬化被覆法(オリフィス法)、液中乾燥法
、噴霧−造粒法等が利用できるが、なかでも界面重合法
、及び]n −5itu法は目的とするDCIPのマイ
クロカプセル化を効果的、かつ経済的に可能ならしめる
ので特に有用である。In the microencapsulation of DCIP in the present invention, the core material is DCIP alone or a mixture containing DCIP, and the outer wall material has a sustained release property that allows adjustment of the volatilization rate of DCIP, and also reduces its medicinal efficacy. A method is used to micro-encapsulate DCIP from a single outer wall. In the microcapsule production technology, widely known interfacial polymerization method, in-5iLu method, phase separation method, in-liquid curing coating method (orifice method), in-liquid drying method, spray-granulation method, etc. can be used. The interfacial polymerization method and the n-5 itu method are particularly useful because they enable microencapsulation of the desired DCIP effectively and economically.
以上の目的を満足するものとしてはモノマー或いは低分
子量のプレポリマー等の反応材料を使用して形成する高
分子材料が特に好ましく、かかる高分子材料としては例
えば、ポリアミド樹脂、ポリエステル樹脂、ポリウレア
樹脂、ポリウレタン樹脂、尿素樹脂、グアナミン樹脂、
メラミン樹脂、及びこれらの複合材料か挙げられる。Particularly preferred as a material that satisfies the above objectives are polymeric materials formed using reactive materials such as monomers or low molecular weight prepolymers; examples of such polymeric materials include polyamide resins, polyester resins, polyurea resins, polyurethane resin, urea resin, guanamine resin,
Examples include melamine resin and composite materials thereof.
本発明に於けるDCIPを含む芯物質と壁月料の好まし
い割合については特に限定されないが、経済性を考慮す
ると直接植物生育促進効果を有しない壁材は少ないこと
が好ましい。しかし本発明のマイクロカプセル壁材は内
包される液体状のDCIPを充分保持すると同時に内包
物を保護しなければならす、自ずと芯物質に対する壁材
の使用量としての下限が限定される。以上から芯物質と
壁材の好ましい重量比は]・1〜]:0.OIであり、
さらに好ましくは1:0.3〜1 : 0.03である
。In the present invention, there is no particular limitation on the preferred ratio of the core substance containing DCIP to the wall material, but in consideration of economic efficiency, it is preferable that the wall material does not have a direct plant growth promoting effect. However, the microcapsule wall material of the present invention must sufficiently retain the encapsulated liquid DCIP and at the same time protect the encapsulated material, which naturally limits the lower limit of the amount of wall material to be used relative to the core material. From the above, the preferred weight ratio of the core material and wall material is ].1 to ]:0. OI,
More preferably, the ratio is 1:0.3 to 1:0.03.
又DCIPの揮発速度を調整して、長期間に亘って植物
の生育促進効果を保持するためには、DCIPを芯材と
するマイクロカプセルの好ましい平均粒径は100μm
以下0.1μm以上、膜厚は10μm以下0.01μm
以上であり、さらに好ましくは508m以下1μm以上
、膜厚は5μm以下0.1μm以上である。In addition, in order to adjust the volatilization rate of DCIP and maintain the effect of promoting plant growth over a long period of time, the preferred average particle size of microcapsules containing DCIP as a core material is 100 μm.
0.1μm or more, film thickness 10μm or less 0.01μm
More preferably, the film thickness is 508 m or less and 1 μm or more, and the film thickness is 5 μm or less and 0.1 μm or more.
本発明のDCIPを内包した徐放性マイクロカプセル化
製剤は植物の特に、ホウレンソウ、イチゴなど野菜、草
花なとの園芸作物、イネ、牧草など普通作物、茶、たば
こなど時用作物、ミカン、りんごなど果樹作物などに対
し長期に亘って生育促進を必要とする場合には、DCI
P量として1〜20g/rd、好ましくは5g/ゴを散
布、土壌処理などによって使用することも可能である。The sustained-release microencapsulated preparation containing DCIP of the present invention can be applied to plants, especially vegetables such as spinach and strawberries, horticultural crops such as flowers, common crops such as rice and grass, occasional crops such as tea and tobacco, mandarin oranges, and apples. When long-term growth promotion is required for fruit crops such as
It is also possible to use P in an amount of 1 to 20 g/rd, preferably 5 g/rd, by spraying, soil treatment, etc.
従って本発明のDCIPを内包した徐放性マイクロカプ
セル化製剤はその使途によりマイクロカプセルの水分散
液自体でも、又粉体にしたものでも、或いは粉体を製剤
化、成形化したものでも広範囲な利用を可能とする。Therefore, the sustained-release microencapsulated preparation containing DCIP of the present invention can be used in a wide range of applications, including an aqueous dispersion of microcapsules, a powder, or a formulation or molding of the powder. make it available for use.
以下、実施例により本発明を更に詳しく説明するか、目
的とするDCIPを内包した徐放性マイクロカプセル化
植物生育促進製剤を得る方法は必ずしもこれ等の実施例
のみに限定されるものではない。なお、この明細書を通
して、温度は全て90であり部及び%は特記しない限り
重量基準である。Hereinafter, the present invention will be explained in more detail with reference to Examples, and the method for obtaining the intended sustained-release microencapsulated plant growth promoting preparation containing DCIP is not necessarily limited to these Examples. Throughout this specification, all temperatures are 90°C and parts and percentages are by weight unless otherwise specified.
実施例 1
DCIP(135部)に対してポリメチレンポリフェニ
ルイソシアネートrMR−200J (商品名、(」
本ポリウレタン社製) (31,6部)を添加して溶
解させた後、2%ポリビビニアルコールrPVA−21
7J (商品名、クラレ社製)溶液(300部)に加
え、バイオミキサー(日本精機社製)にてエマルション
の粒径が20μmとなるように乳化を行なった。得られ
た乳化物をゆっくり撹拌しながら、水(40部)に対し
てジエチレントリアミン(3部)をfめ溶解させた水溶
液を徐々に添加し、約20時間室温にて撹拌を続は反応
を充分行なわせてDCIPを内包した徐放性のポリウレ
ア壁マイクロカプセル分散液を得た。Example 1 DCIP (135 parts) to polymethylene polyphenylisocyanate rMR-200J (trade name, ()
After adding and dissolving 2% polyvinyl alcohol rPVA-21 (produced by Honpolyurethane Co., Ltd.) (31.6 parts),
In addition to 7J (trade name, manufactured by Kuraray Co., Ltd.) solution (300 parts), emulsification was carried out using a biomixer (manufactured by Nippon Seiki Co., Ltd.) so that the particle size of the emulsion was 20 μm. While slowly stirring the resulting emulsion, an aqueous solution of diethylenetriamine (3 parts) dissolved in water (40 parts) was gradually added, and the mixture was stirred at room temperature for about 20 hours until the reaction was sufficiently controlled. This was carried out to obtain a sustained release polyurea wall microcapsule dispersion containing DCIP.
実施例 2
DCIP(135部)にテレフタル酸クロライド(10
部)を加えて溶解させた後、3%ポリビニルアルコール
rPVA−217J (商品名、クラレ社製)溶液(
300部)中に加え、バイオミキサーにてエマルジョン
の粒径が20μmとなるように乳化を行なった。Example 2 Terephthalic acid chloride (10 parts) was added to DCIP (135 parts).
After adding and dissolving 3% polyvinyl alcohol rPVA-217J (trade name, manufactured by Kuraray Co., Ltd.) solution (
300 parts) and emulsified in a biomixer so that the particle size of the emulsion was 20 μm.
得られた乳化物をゆっくり撹拌しながら、水(70部)
中にエチレンジアミン(3,4部)及びソーダ灰(6部
)を予め溶解させた水溶液を徐々に添加し、約20時間
室温にて撹拌を続け、反応を充分に行なわせ、DCIP
を内包した徐放性のポリアミド壁マイクロカプセル分散
液を得た。While slowly stirring the resulting emulsion, add water (70 parts).
An aqueous solution in which ethylenediamine (3,4 parts) and soda ash (6 parts) were dissolved in advance was gradually added to the solution, and stirring was continued at room temperature for about 20 hours to ensure a sufficient reaction.
A sustained-release polyamide-walled microcapsule dispersion containing the following was obtained.
実施例 3
37%ホルマリン溶液(488,5g)に尿素(240
部)を溶解し、トリエタノールアミンにてpH8,0に
調整した後、70℃、1時間、加熱、撹拌した。水(1
00部)を加え、尿素−ホルムアルデヒドのプレポリマ
ーを用意した。Example 3 Urea (240 g) was added to 37% formalin solution (488.5 g).
After dissolving the solution and adjusting the pH to 8.0 with triethanolamine, the mixture was heated and stirred at 70°C for 1 hour. Water (1
00 parts) to prepare a urea-formaldehyde prepolymer.
上記プレポリマー溶液(80部)のpHを10%クエン
酸水溶液にて4.2に調整した後、バイオミキサーにて
乳化を行ないながらDCIP(65部)を加え、さらに
この乳化物のpHを10%クエン酸水溶液で3.5にし
た後、徐々に昇温をして40〜45℃にて40分撹拌し
た。温水(50部)をさらに加え、3時間撹拌して冷却
し、DCIPを内包した尿素ホルマリン樹脂壁マイクロ
カプセル分散液を得た。After adjusting the pH of the prepolymer solution (80 parts) to 4.2 with a 10% citric acid aqueous solution, DCIP (65 parts) was added while emulsifying with a biomixer, and the pH of this emulsion was adjusted to 10. After adjusting the temperature to 3.5% with an aqueous solution of citric acid, the temperature was gradually raised and stirred at 40 to 45°C for 40 minutes. Warm water (50 parts) was further added, and the mixture was stirred for 3 hours and cooled to obtain a urea-formalin resin-walled microcapsule dispersion containing DCIP.
比較例 1
2%ポリビビニアルコールrPVA−217J(商品名
、クラレ社製)溶液(100部)にDCIP(25部)
を加えた。Comparative Example 1 DCIP (25 parts) in 2% polyvinyl alcohol rPVA-217J (trade name, manufactured by Kuraray Co., Ltd.) solution (100 parts)
added.
比較例 2
DCIP(85部)にツルポール2613B (商品名
、東邦化学製)(5部)、白灯油(10部)を加え、混
合撹拌して均質なサンプルとした。Comparative Example 2 To DCIP (85 parts), Tsurupol 2613B (trade name, manufactured by Toho Chemical Co., Ltd.) (5 parts) and white kerosene (10 parts) were added and mixed and stirred to prepare a homogeneous sample.
〈カプセル内DCIP量の測定方法〉
実施例1〜3にて得られたDCIPを内包したマイクロ
カプセルの分散液を所定量採取し、アセトンを加えた。<Method for Measuring the Amount of DCIP in a Capsule> A predetermined amount of the microcapsule dispersion containing DCIP obtained in Examples 1 to 3 was collected, and acetone was added.
超音波槽中にてDCIPを抽出しメンブランフィルタ−
で濾過後、濾液を分析に供した。Extract DCIP in an ultrasonic bath and filter it with a membrane filter.
After filtration, the filtrate was subjected to analysis.
〈徐放性評価方法〉
実施例1〜3、比較例1,2にて古られたDCIP分散
液のサンプルについては、DCIP換算で約0.8 g
/ 100cIilとなるようにシャーレ全体に均一
に拡げた。各サンプルを25℃雰囲気中に静置し一定期
間経過後、DCIPの残存率を上記の方法によって測定
した。<Sustained release evaluation method> Regarding the samples of the DCIP dispersion liquids used in Examples 1 to 3 and Comparative Examples 1 and 2, approximately 0.8 g in terms of DCIP
/ 100cIil was spread uniformly over the entire Petri dish. Each sample was left standing in an atmosphere at 25° C., and after a certain period of time, the residual rate of DCIP was measured by the method described above.
DCIP内包マイクロカプセルの徐放性(DCIP残存
率%)
〈試験 例〉
試験例 1
実施例1,2および3に基づき作製されたDCIP徐放
性マイクロカプセル製剤と比較例1゜2に基づき作製さ
れたDCIP製剤のホウレンソウに対する生育促進作用
を比較した。Sustained-release properties of DCIP-containing microcapsules (DCIP residual rate %) <Test examples> Test example 1 DCIP sustained-release microcapsule formulations prepared based on Examples 1, 2, and 3 and those prepared based on Comparative Example 1゜2. The growth promoting effects of the DCIP formulations on spinach were compared.
土壌をつめた1/2000aポツトの中央約15cmの
深さの位置にDCIP各製剤の4kga、i/loa相
当量を処理した。その後ホウレンソウ種子をポット当り
15粒播種し、発芽揃期に間引きを行ないポット当り7
株にそろえた。試験は3反復とした。An amount equivalent to 4 kg, i/loa of each DCIP preparation was applied to the center of a 1/2000a pot filled with soil at a depth of about 15 cm. After that, 15 spinach seeds were sown per pot, and thinned out at the germination stage, resulting in 7 seeds per pot.
Aligned with stocks. The test was repeated three times.
収穫期にすべての株を抜き取り、葉長、地上部組および
根重を測定した。All plants were pulled out during the harvest period, and leaf length, aboveground composition, and root weight were measured.
結 果
試験例 2
実施例1,2および3に基づき作製されたDCIP徐放
性マイクロカプセル製剤と比較例1゜2に基づき作製さ
れたDCIP製剤のイチゴに対する生育促進作用を比較
した。Results Test Example 2 The growth promoting effect on strawberries of the DCIP sustained release microcapsule preparations prepared based on Examples 1, 2, and 3 and the DCIP preparation prepared based on Comparative Example 1.2 was compared.
促成イチゴハウスに上記の各製剤をDCIP換算で8k
g/lOaになるように土壌混和し、7日後に常法によ
り定植した。供試株数は1区20株で2反復とし、定植
後約4ケ月後の各区収量を合計し、平均株当り収量を求
めた。Each of the above preparations is added to the accelerated strawberry house at DCIP equivalent of 8k.
The soil was mixed to a concentration of g/lOa, and 7 days later, the plants were planted using a conventional method. The number of test plants was 20 per plot and repeated twice, and the yields of each plot about 4 months after planting were totaled to determine the average yield per plant.
結 果 出 願人 株式会社ニス・デイ φニス バイオチック 1 ]result Out applicant Niss Day Co., Ltd. φ varnish biotic 1]
Claims (1)
つ該有効成分を芯材とし、且つ該芯材の周囲に形成され
た壁材によって該芯材が徐放出することを特徴とするマ
イクロカプセル化された植物生育促進製剤。A microencapsulated plant growth material comprising dichlordiisopropyl ether as an active ingredient, the active ingredient as a core material, and a wall material formed around the core material to allow sustained release of the core material. Accelerator formulation.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13253890A JPH0429904A (en) | 1990-05-24 | 1990-05-24 | Plant growth-promotive preparation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13253890A JPH0429904A (en) | 1990-05-24 | 1990-05-24 | Plant growth-promotive preparation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0429904A true JPH0429904A (en) | 1992-01-31 |
Family
ID=15083620
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13253890A Pending JPH0429904A (en) | 1990-05-24 | 1990-05-24 | Plant growth-promotive preparation |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0429904A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002066307A (en) * | 2000-08-29 | 2002-03-05 | Kureha Chem Ind Co Ltd | Microcapsule granular material and method of manufacturing the same |
| WO2008155097A3 (en) * | 2007-06-21 | 2009-10-01 | Syngenta Participations Ag | Method of improving the growth of a plant |
-
1990
- 1990-05-24 JP JP13253890A patent/JPH0429904A/en active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002066307A (en) * | 2000-08-29 | 2002-03-05 | Kureha Chem Ind Co Ltd | Microcapsule granular material and method of manufacturing the same |
| WO2008155097A3 (en) * | 2007-06-21 | 2009-10-01 | Syngenta Participations Ag | Method of improving the growth of a plant |
| JP2010530394A (en) * | 2007-06-21 | 2010-09-09 | シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト | How to improve plant growth |
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