JPS6328043B2 - - Google Patents

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Publication number
JPS6328043B2
JPS6328043B2 JP54118126A JP11812679A JPS6328043B2 JP S6328043 B2 JPS6328043 B2 JP S6328043B2 JP 54118126 A JP54118126 A JP 54118126A JP 11812679 A JP11812679 A JP 11812679A JP S6328043 B2 JPS6328043 B2 JP S6328043B2
Authority
JP
Japan
Prior art keywords
disease
fatty acid
test
composition
polyglycerol fatty
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.)
Expired
Application number
JP54118126A
Other languages
Japanese (ja)
Other versions
JPS5643207A (en
Inventor
Asatada Misato
Yasuo Pponma
Yutaka Arimoto
Tooru Hidaka
Mitsuharu Juta
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.)
RIKEN Institute of Physical and Chemical Research
Original Assignee
RIKEN Institute of Physical and Chemical Research
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 RIKEN Institute of Physical and Chemical Research filed Critical RIKEN Institute of Physical and Chemical Research
Priority to JP11812679A priority Critical patent/JPS5643207A/en
Publication of JPS5643207A publication Critical patent/JPS5643207A/en
Publication of JPS6328043B2 publication Critical patent/JPS6328043B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、炭酸水素ナトリウムとポリグリセロ
ール脂肪酸エステルの1種又は2種以上とを有効
成分として含有する安全性の極めて高いすぐれた
農園芸用殺菌剤及び植物ウイルス病害防除剤組成
物に関するものである。 従来、農園芸用殺菌剤として銅剤、水銀剤、砒
素剤のような重金属化合物及び有機塩素系薬剤や
有機燐酸系薬剤が広く用いられて来たが、これら
の薬剤は、いずれも人体や動物に有害であり、ま
た土壤に対する汚染など、いわゆる環境汚染が重
大な社会問題となつている。 このような現状から、人体や動・植物に対して
安全性の高い農園芸用殺菌剤の新たな開発が強く
望まれているが、本発明者らは、安全性が極めて
高く、且つ植物病害に対して顕著な防除効果を示
す薬剤の開発について鋭意研究の結果、炭酸水素
ナトリウム及びポリグリセロール脂肪酸エステル
を有効成分として含有する薬剤が各種植物病害、
果実貯蔵病害及び植物ウイルス病害に対してすぐ
れた相乗的防除効果を奏し、且つ施用時の取扱い
が便利で、植物体に何らの悪影響を及ぼさないこ
との新たな知見を得て、こゝに本発明を完成する
に至つた。 本発明組成物の有効成分の一つである炭酸水素
ナトリウムは、医薬、ベーキングパウダー等の食
品用膨剤として広く用いられているほか、その植
物病害に対する防除効果により、殺菌剤としても
用い得る。しかし、これを殺菌剤として単独で使
用した場合には、その水溶性のために表面張力が
増大し、また植物体上において結晶が折出するた
めに植物体への展着性が劣り、持続して十分な病
害防除効果を発揮し得ないという問題を有する。
しかも、その展着性を向上させるために、界面活
性作用を有する種々の担体物質を組合わせて使用
しても、両者の親和性と展着性の向上による防除
作用の改善とは必ずしも一致せず、この問題を解
決するまでには至つていない。 一方、本発明組成物の他の有効成分であるポリ
グリセロール脂肪酸エステルは、各種植物病害の
防除に単独で用いた場合には、その効果は全く不
十分で、有効な防除薬剤とはなり得ない。 しかしながら、ポリグリセロール脂肪酸エステ
ルは分子内に適度の親水性と親油性を有している
ために水に容易に分散ないし溶解する性質をもつ
ている。本発明者らはこれに着目し、ポリグリセ
ロール脂肪酸エステルを炭酸水素ナトリウムと組
合せることによつて、炭酸水素ナトリウム水溶液
の表面張力を低下させて植物体への展着性を増大
させると共に、植物体上に散布された炭酸水素ナ
トリウムの結晶の折出を防止して両成分を植物体
上に均一に保持し得ることの知見を得て、両成分
の薬剤成分としての欠点を相補完した本発明のす
ぐれた組成物を完成するに至つた。即ち、本発明
の組成物は前記各成分の単独施用の場合に比し、
各種植物病害に対して相乗的に顕著な防除効果が
持続性よく得られるものである。 本発明殺菌組成物の対象病害としては、イネい
もち病、絞枯病、ミカンの青緑かび病、灰色かび
病、黒点病、かいよう病、キユウリのうどんこ
病、炭疽病、べと病、斑点性細菌病、トマトの葉
かび病、ぶどうのばんぷ病等の植物病害、果実、
とくにかんきつ類の各種貯蔵病害及びトマトモザ
イクウイルス病等の植物ウイルス病害が挙げられ
る。 さらに、本発明の著しい効果として本発明組成
物の有効成分がいずれも食品添加物として認めら
れている無害物質であり、従つてこれに加える担
体、溶剤、補助剤等に食品添加物等の安全性の高
い物質を選べば、本発明組成物を完全無公害農薬
とすることができる。従つて本発明は、取扱上の
危険性の全くない、また作物への残留毒性や環境
汚染の懸念の全くない、すぐれた殺菌剤を提供す
ることができる。 更に本発明組成物は、有効成分を組合わせるこ
とによつて、容易に展着性のすぐれた水和剤に製
剤化し、施用効果を著しく高めることができる。 このように、本発明組成物の効果は、対象病害
植物の適用範囲を拡大し、各有効成分の植物病害
防除効果を相乗的に高め、且つその高い治療効果
を持続的に安定化させ得ることである。しかもそ
の製剤化が容易で、施用時の不便を全く生じない
という極めて特異的な作用をも発揮し得るもので
ある。 本発明の組成物の一成分、ポリグリセロール脂
肪酸エステルは、グリセリンの脱水縮合体である
ポリグリセロールと油脂構成成分である脂肪酸と
のエステルであり、次の構造式で表わされる。 〔但し、R1、R2、R3の少なくとも1個以上は脂
肪酸であり、他は水素を表わす。nは2以上(好
ましくは2〜10)を示す。〕 ポリグリセロールは、グリセリンを加熱脱水縮
合させることによつて重合度2〜30のものが得ら
れる他、合成グリセリンと同様の方法で合成する
こともできる。グリセリンが3個の水酸基を含む
のに対し、ジグリセロールは4個、トリグリセロ
ールは5個であり、重合モル数が増すにつれて水
酸基は1個づつ増大して親水性を増す。なお、重
合度は2〜30で、特に2〜10が好ましい。 一方、ポリグリセロール脂肪酸エステルを構成
する脂肪酸成分としては、炭素数8〜22の飽和脂
肪酸、例えばカプリル酸、カプリン酸、ラウリン
酸、ミスチリン酸、パルミチン酸、ステアリン
酸、アラキン酸、ベヘニン酸、または不飽和脂肪
酸、例えばオレイン酸、リノール酸、リノレン
酸、リシノレン酸等の単一脂肪酸の他、混合脂肪
酸、例えば牛脂、綿実油、ナタネ油、パーム油等
の天然動植物油及びこれらの硬化油よりの混合脂
肪酸が用いられる。これらの脂肪酸は、飽和脂肪
酸より不飽和脂肪酸が特に良く、且つモノエステ
ル含量の多いもの程、即ち遊離の水酸基を多く含
むもの程好適に用いられる。また、ポリグリセロ
ール脂肪酸エステルは、ポリグリセロールの水酸
基の数だけ脂肪酸をエステル化することができ
る。例えば、ジグリセロールはテトラ脂肪酸エス
テル、トリグリセロールはペンタ脂肪酸エステル
まで作り得るので、グリセリンの重合度、脂肪酸
の種類または脂肪酸の結合量により多種のエステ
ルを作ることができる。従つて、疎水性のものか
ら水に可溶の親水性の強いものまで任意に作るこ
とが可能である。 グリセリン脂肪酸エステルが水酸基を最高2個
しか含まず、疎水性であるために水に分散させる
に際して特殊な条件が必要であるのに対し、上記
のポリグリセロール脂肪酸エステルは、水酸基の
数を任意に変え得るので、水に容易に分散するも
のから完全に溶解するものまで所望に応じて任意
に作り得る利点がある。またその安全性について
は各国においた食品添加物として加工食品の乳化
剤、品質改良剤等に汎用されていることからも明
らかなように、安全性の極めて高いことが認めら
れている。 これらのポリグリセロール脂肪酸エステルはそ
の1種、又は2種以上を混合して、加温溶融する
か、又はアルコール、プロピレングリコール、グ
リセリン、ソルビトール等の食品添加物として認
可されている溶剤又はこれらの混合溶剤に溶解し
たのち、これを炭酸水素ナトリウム粉末と混合す
ることにより、炭酸水素ナトリウムの結晶粒子を
ポリグリセロール脂肪酸エステルでコーテイング
した粉末を作ることができる。また、前記ポリグ
リセロール脂肪酸エステルの1種又は2種以上
を、あらかじめ水に分散し、これに例えばデンプ
ン、CMC、アルギン酸ソーダ、カゼインソーダ
等の親水性コロイド物質である食品又は食品添加
物を加え、これを乾燥粉末化することにより、こ
れらのポリグリセロール脂肪酸エステルは親水性
コロイド物質と親和し、冷水にも容易に分散し得
る粉末となり、これに炭酸水素ナトリウム粉末を
混合して好適に本発明組成物の有効成分粉末とす
ることができる。 本発明組成物の有効成分は、これに適当な担体
を加えて水和剤、粉剤及び粒剤等の各種剤型に製
剤化することができる。ここにいう担体として
は、クレー、ホワイトカーボン、珪藻土、カオリ
ン、タルク及びシリカ等を挙げることができる。 また、農薬組成物に一般に使用されている補助
剤、例えば展着剤、湿展剤、固着剤等の界面活性
剤は、本発明組成物の有効成分の水和性をより高
めるために有効であり、例えばアルキルアリルス
ルホネート、ポリオキシエチレンアルキルアリル
スルホネート等を適宜添加して易溶性の水和剤に
容易に製剤化することができる。 更に、本発明の組成物は、その効果を減少させ
る作用を生じない限り、他の農薬、例えば殺菌
剤、殺虫剤、植物生長調節剤、除草剤等と適宜混
合したり、併用することは何ら差支えない。 本発明組成物における有効成分のポリグリセロ
ール脂肪酸エステルの総量と炭酸水素ナトリウム
との混合重量比は、とくに限定されるものではな
いが10:1ないし1:10、好ましくは8:2〜
2:8の範囲で適宜決めることができる。 また、本発明組成物中の有効成分総量の割合は
水和剤で10〜90%、粉剤で0.1〜20%程度が適当
であるが、これに限定されることなく、使用目的
に応じて適宜増減することができる。 次に、本発明の組成物について実施例を挙げる
が、本発明はこれによつて何ら限定されるもので
はない。 実施例 1 (水和剤) 炭酸水素ナトリウム80重量部に対し、デカグリ
セロールトリラウリン酸エステル20重量部を50℃
で混合し、表面に吸着されることによつて流動性
の良い水和剤を得る。 実施例 2 (水和剤) トリグリセロールジ大豆油脂肪酸エステル30重
量部を50℃で珪藻土100重量部と混合し、吸着さ
せて粉末とし、これに炭酸水素ナトリウム70部を
混合して流動性の良い水和剤を得る。 実施例 3 (水和剤) ジグリセロールモノオレート80重量部と、別途
150重量部の水に10重量部のCMCを溶解したもの
を混合し、70℃まで加温して均一な分散液とす
る。これを噴霧乾燥機を用いて乾燥して粉末とす
る。この粉末50重量部に対して炭酸水素ナトリウ
ム50重量部を混合して流動性の良い水和剤を得
る。 上記実施例により調製される組成物は、互いに
親和性の良好な炭酸水素ナトリウム及びポリグリ
セロール脂肪酸エステルの両有効成分がその展着
性、分散性の著しい向上と相まつて、相乗的に顕
著な優れた殺菌効果を持続的に安定に発揮する。
例えば、かんきつ類等の果実貯蔵病害の場合、炭
酸水素ナトリウムを単独で用いたときの防除価
は、平均的に約60%程度であり、病害が激発状態
になる程防除価は相対的に低下する傾向を示すの
に対して、本発明組成物の有効成分の組合せによ
るときは、防除効果は極めて安定化され、病害が
激発状態においてもほぼ100%の防除価が持続的
に再現性よく得られる。また、イネいもち病、ミ
カン黒点病、キユウリ炭疽病、うどんこ病等の疏
菜類のかび病害に対しても前記果実貯蔵病害の場
合と同様な結果が得られる上、トマトモザイクウ
イルス病等の植物ウイルス病害に対しても同様の
すぐれた結果が得られる。 次に、本発明組成物の各種植物病害防除効果に
ついて試驗例を示す。 試驗例 1 (ミカン貯蔵病害防除試験) 1区当り10〜25果の供試果(温州ミカン)を木
綿針で油胞内(深さ:1.5mm)付傷した。1果当
りの付傷部位は4個所とし、以下の薬剤毎に4ブ
ロツクを設けた。 付傷後、ミカン縁かび病原菌(Penicillium
digltatum)胞子懸濁液を供試果の付傷部位に噴
霧接種した。2時間後に実施例1〜3に準じて調
製した水和剤の所定濃度希釈液に前記供試果を約
5分間浸漬し、風乾後、この処理果を湿度ほぼ
100%に保ち、4〜6日後にその病害の発生状態
を調べた。一方、対照薬剤として炭酸水素ナトリ
ウム及び各種ポリグリセロール脂肪酸エステルを
それぞれ単独で用いて同様に処理した。各供試薬
剤について病害の程度を調べ、次式に従つて防除
価を算出した。 防除価(%)=(1−処理区の病斑数/無処理区の病斑
数)×100 この結果を第1表に示す。
The present invention relates to an excellent, extremely safe agricultural and horticultural fungicide and plant virus disease control agent composition containing sodium bicarbonate and one or more polyglycerol fatty acid esters as active ingredients. . Conventionally, heavy metal compounds such as copper agents, mercury agents, and arsenic agents, as well as organic chlorine agents and organic phosphoric acid agents, have been widely used as disinfectants for agriculture and horticulture, but all of these agents are harmful to humans and animals. In addition, so-called environmental pollution, such as soil contamination, has become a serious social problem. Given this current situation, there is a strong desire to develop new agricultural and horticultural fungicides that are highly safe for humans, animals, and plants. As a result of intensive research into the development of drugs that have remarkable control effects on various plant diseases, drugs containing sodium bicarbonate and polyglycerol fatty acid ester as active ingredients have been found to be effective against various plant diseases.
Having obtained new knowledge that it has an excellent synergistic control effect against fruit storage diseases and plant virus diseases, is convenient to handle during application, and does not have any adverse effects on plants, we have published this book. The invention was completed. Sodium hydrogen carbonate, which is one of the active ingredients of the composition of the present invention, is widely used as a leavening agent for medicines and foods such as baking powder, and can also be used as a fungicide due to its effect on controlling plant diseases. However, when used alone as a fungicide, the surface tension increases due to its water solubility, and crystals are precipitated on the plant, resulting in poor spreadability and long-lasting However, there is a problem in that it cannot exhibit sufficient disease control effects.
Moreover, even if various carrier substances with surfactant properties are used in combination to improve the spreadability, the improvement in the pesticidal effect due to the improvement in the affinity and spreadability of the two does not necessarily match. However, we have not yet reached the point of solving this problem. On the other hand, when polyglycerol fatty acid ester, which is another active ingredient of the composition of the present invention, is used alone to control various plant diseases, its effect is completely insufficient and it cannot be an effective control agent. . However, polyglycerol fatty acid esters have moderate hydrophilicity and lipophilicity in their molecules, so they have the property of easily dispersing or dissolving in water. The present inventors focused on this, and by combining polyglycerol fatty acid ester with sodium hydrogen carbonate, the surface tension of the sodium hydrogen carbonate aqueous solution was lowered and the spreadability to plants was increased. This book complements the shortcomings of both components as medicinal components by obtaining the knowledge that both components can be maintained uniformly on the plant body by preventing the crystallization of sodium bicarbonate sprayed on the plant body. An excellent composition of the invention has been completed. That is, the composition of the present invention, compared to the case where each of the above-mentioned components is applied alone,
A remarkable synergistic control effect against various plant diseases can be obtained in a sustained manner. Target diseases of the fungicidal composition of the present invention include rice blast, strangle blight, blue-green mold of tangerine, gray mold, black spot, canker blight, powdery mildew of cucumber, anthracnose, downy mildew, and leaf spot. Plant diseases such as bacterial diseases, tomato leaf mold, and grape blight, fruit,
In particular, various storage diseases of citrus fruits and plant virus diseases such as tomato mosaic virus disease can be mentioned. Furthermore, as a remarkable effect of the present invention, all of the active ingredients of the composition of the present invention are harmless substances that are recognized as food additives, and therefore, the carriers, solvents, adjuvants, etc. added to them are safe to use as food additives. By selecting a substance with high properties, the composition of the present invention can be made into a completely pollution-free pesticide. Therefore, the present invention can provide an excellent fungicide that is completely free from handling hazards and has no concerns about residual toxicity to crops or environmental contamination. Furthermore, by combining the active ingredients, the composition of the present invention can be easily formulated into a wettable powder with excellent spreadability, and the application effect can be significantly enhanced. As described above, the effects of the composition of the present invention are that it can expand the range of application to target diseased plants, synergistically enhance the plant disease control effects of each active ingredient, and sustainably stabilize its high therapeutic effects. It is. In addition, it is easy to formulate a formulation and can exhibit extremely specific effects without causing any inconvenience during application. One component of the composition of the present invention, polyglycerol fatty acid ester, is an ester of polyglycerol, which is a dehydrated condensation product of glycerin, and fatty acid, which is an oil component, and is represented by the following structural formula. [However, at least one of R 1 , R 2 , and R 3 is a fatty acid, and the others represent hydrogen. n represents 2 or more (preferably 2 to 10). ] Polyglycerol having a degree of polymerization of 2 to 30 can be obtained by subjecting glycerin to thermal dehydration condensation, and can also be synthesized by the same method as synthetic glycerin. While glycerin contains three hydroxyl groups, diglycerol has four and triglycerol has five, and as the number of polymerized moles increases, the number of hydroxyl groups increases by one, increasing hydrophilicity. In addition, the degree of polymerization is 2 to 30, particularly preferably 2 to 10. On the other hand, the fatty acid components constituting the polyglycerol fatty acid ester include saturated fatty acids having 8 to 22 carbon atoms, such as caprylic acid, capric acid, lauric acid, mystilic acid, palmitic acid, stearic acid, arachidic acid, behenic acid, and Saturated fatty acids, such as single fatty acids such as oleic acid, linoleic acid, linolenic acid, and ricinolenic acid, as well as mixed fatty acids, such as natural animal and vegetable oils such as beef tallow, cottonseed oil, rapeseed oil, and palm oil, and mixed fatty acids from these hydrogenated oils. is used. Among these fatty acids, unsaturated fatty acids are particularly better than saturated fatty acids, and the higher the monoester content, that is, the higher the free hydroxyl group content, the more preferably they are used. Furthermore, the polyglycerol fatty acid ester can esterify as many fatty acids as the number of hydroxyl groups in polyglycerol. For example, diglycerol can be made into a tetra fatty acid ester, and triglycerol can be made into a penta fatty acid ester, so a wide variety of esters can be made depending on the degree of polymerization of glycerin, the type of fatty acid, or the amount of fatty acid bonded. Therefore, it is possible to make any desired material from hydrophobic to water-soluble and highly hydrophilic. Glycerol fatty acid ester contains only two hydroxyl groups at most and is hydrophobic, so special conditions are required when dispersing it in water, whereas the above polyglycerol fatty acid ester can have any number of hydroxyl groups. Since it can be obtained, it has the advantage that it can be made as desired, from easily dispersible to completely soluble in water. Furthermore, it is recognized to be extremely safe, as evidenced by the fact that it is widely used as a food additive in various countries, such as as an emulsifier and quality improver for processed foods. These polyglycerol fatty acid esters can be used by heating and melting one or more of them, or by using a solvent approved as a food additive such as alcohol, propylene glycol, glycerin, or sorbitol, or a mixture thereof. By dissolving it in a solvent and mixing it with sodium bicarbonate powder, it is possible to produce a powder in which sodium bicarbonate crystal particles are coated with polyglycerol fatty acid ester. Alternatively, one or more of the polyglycerol fatty acid esters are dispersed in water in advance, and a food or food additive, which is a hydrophilic colloid substance such as starch, CMC, sodium alginate, or casein soda, is added thereto; By drying and powdering these polyglycerol fatty acid esters, these polyglycerol fatty acid esters become powders that have an affinity with hydrophilic colloid substances and can be easily dispersed in cold water.Sodium hydrogen carbonate powder is mixed with this to form the composition of the present invention. It can be made into a powder of active ingredients. The active ingredient of the composition of the present invention can be formulated into various dosage forms such as wettable powders, powders, and granules by adding a suitable carrier thereto. Examples of the carrier herein include clay, white carbon, diatomaceous earth, kaolin, talc, and silica. In addition, adjuvants commonly used in agrochemical compositions, such as surfactants such as spreading agents, wetting agents, and fixing agents, are effective in increasing the hydration of the active ingredients of the composition of the present invention. For example, by appropriately adding alkylaryl sulfonate, polyoxyethylene alkylaryl sulfonate, etc., it can be easily formulated into easily soluble wettable powders. Furthermore, the composition of the present invention may not be appropriately mixed or used in combination with other agricultural chemicals, such as fungicides, insecticides, plant growth regulators, herbicides, etc., as long as this does not reduce their effectiveness. No problem. The mixing weight ratio of the total amount of polyglycerol fatty acid ester as an active ingredient to sodium hydrogen carbonate in the composition of the present invention is not particularly limited, but is 10:1 to 1:10, preferably 8:2 to
It can be determined as appropriate within the range of 2:8. In addition, the proportion of the total amount of active ingredients in the composition of the present invention is suitably about 10 to 90% for wettable powders and about 0.1 to 20% for powdered powders, but is not limited to this and can be adjusted as appropriate depending on the purpose of use. It can be increased or decreased. Next, Examples will be given regarding the composition of the present invention, but the present invention is not limited thereto. Example 1 (Wettable powder) 20 parts by weight of decaglycerol trilaurate was added to 80 parts by weight of sodium hydrogen carbonate at 50°C.
A wettable powder with good fluidity is obtained by adsorption on the surface. Example 2 (Wettable powder) 30 parts by weight of triglycerol di-soybean oil fatty acid ester was mixed with 100 parts by weight of diatomaceous earth at 50°C, adsorbed to form a powder, and 70 parts of sodium bicarbonate was mixed thereto to form a fluid powder. Get a good hydrating agent. Example 3 (Wettable powder) 80 parts by weight of diglycerol monooleate and separately
A solution of 10 parts by weight of CMC in 150 parts by weight of water is mixed and heated to 70°C to form a uniform dispersion. This is dried using a spray dryer to form a powder. 50 parts by weight of sodium bicarbonate is mixed with 50 parts by weight of this powder to obtain a wettable powder with good fluidity. The composition prepared according to the above example has remarkable synergistic properties due to the fact that both active ingredients, sodium hydrogen carbonate and polyglycerol fatty acid ester, which have good affinity for each other, have significantly improved spreadability and dispersibility. It continuously and stably exhibits a bactericidal effect.
For example, in the case of fruit storage diseases such as citrus fruits, the control value when using sodium bicarbonate alone is about 60% on average, and the control value decreases relatively as the disease becomes more severe. On the other hand, when the active ingredients of the composition of the present invention are combined, the control effect is extremely stabilized, and almost 100% control value can be obtained continuously and with good reproducibility even when the disease is in an aggressive state. . In addition, results similar to those for fruit storage diseases mentioned above can be obtained against fungal diseases of cane crops such as rice blast, citrus black spot, cucumber anthracnose, and powdery mildew. Similar excellent results can be obtained against plant virus diseases. Next, test examples will be shown regarding the effect of controlling various plant diseases of the composition of the present invention. Test Example 1 (Mandarin orange storage disease control test) 10 to 25 test fruits (Unshu mandarin orange) per plot were injured inside the oil sac (depth: 1.5 mm) with a cotton needle. There were four injured areas per fruit, and four blocks were provided for each of the following drugs. After injury, tangerine edge mold pathogen (Penicillium
digitatum) spore suspension was spray inoculated onto the injured site of the test fruit. After 2 hours, the test fruit was immersed in a predetermined concentration diluted solution of a hydrating agent prepared according to Examples 1 to 3 for about 5 minutes, and after air-drying, the treated fruit was dried at a humidity of approximately
The temperature was maintained at 100%, and the state of disease development was examined 4 to 6 days later. On the other hand, sodium bicarbonate and various polyglycerol fatty acid esters were used alone as control agents and treated in the same manner. The degree of disease damage was investigated for each test drug, and the control value was calculated according to the following formula. Control value (%) = (1 - number of lesions in treated area/number of lesions in untreated area) x 100 The results are shown in Table 1.

【表】【table】

【表】 試驗例 2 (キユウリうどんこ病害防除試驗) キユウリ(品種:相模半白)の2週間生育の幼
苗(2寸鉢〜2本植)に実施例1〜3に準じて調
製した水和剤の所定農度希釈液を、2鉢当り40ml
を均一に噴霧散布して乾燥した後、密室でキユウ
リうどんこ病原菌(Sphaerotheca fuliginea)の
胞子を人為的に風媒接種した。なお、処理区は25
鉢を1ブロツクとする5ブロツクとした。 接種後、10〜14日間温室に保つて発病させ、そ
の発病の速度を調査した。 一方、対照薬剤として炭酸水素ナトリウム及び
各種ポリグリセロール脂肪酸エステルをそれぞれ
単独で用いて同様の処理を行つた。供試薬剤につ
いてそれぞれ発病の程度を調べ、試驗例1の場合
と同様に防除価を算出した。 この結果を第2表に示す。
[Table] Test Example 2 (Test for controlling powdery mildew disease on cucumber) Hydration prepared according to Examples 1 to 3 was applied to two-week-grown seedlings (planted in 2-inch pots to 2 plants) of cucumber (variety: Sagami Hanshiro). 40ml of diluted solution of the specified agricultural agent per 2 pots.
After uniformly spraying and drying, spores of cucumber powdery mildew pathogen (Sphaerotheca fuliginea) were artificially inoculated with air pollination in a closed room. There are 25 treatment areas.
There were 5 blocks, one block being a pot. After inoculation, the plants were kept in a greenhouse for 10 to 14 days to develop disease, and the speed of disease development was investigated. On the other hand, similar treatments were carried out using sodium hydrogen carbonate and various polyglycerol fatty acid esters as control agents. The degree of disease onset was investigated for each test drug, and the control value was calculated in the same manner as in Test Example 1. The results are shown in Table 2.

【表】【table】

【表】 試驗例 3 (イネいもち病害防除試驗) 直径6cmの合成樹脂製ポツトで、1ポツト10株
宛、イネ(品種:十石)を温室内で育成し、第4
葉期において実施例1〜3に準じて調製した水和
剤を所定濃度に希釈したものを、1ポツト当り40
mlずつスプレーガンで稲体に散布した。 散布液が乾いた後、別途もみがら培地(粉末酵
素、エキス、可溶性でんぷん、しよ糖、もみがら
を含む。)で培養したイネいもち病菌
(Pyriculariaoryzae)の胞子を水で懸濁して稲体
に均一に噴霧接種し、温度27℃、湿度95%以上の
恒温恒湿箱に入れて発病させた。接種4日目にお
いて一葉当りの病斑数を求め、次式に従つて防除
価を算出した。 一方、対照薬剤として炭酸水素ナトリウム及び
各種ポリグリセロール脂肪酸エステルをそれぞれ
単独で用いて同様に処理し、それぞれの発病の程
度を調べ、防除価を算出した。 防除価(%)=(1−散布区の病斑数/無散布区の病斑
数)×100 その結果を第3表に示す。
[Table] Test example 3 (Rice blast disease control test) Rice (variety: Jukoku) was grown in a greenhouse in synthetic resin pots with a diameter of 6 cm, with 10 plants per pot.
At the leaf stage, the wettable powder prepared according to Examples 1 to 3 was diluted to a specified concentration, and 40% of the water was added per pot.
ml each was sprayed onto the rice plants using a spray gun. After the spray solution has dried, spores of the rice blast fungus (Pyricularia oryzae), which were separately cultured in a rice husk medium (containing powdered enzymes, extracts, soluble starch, sucrose, and rice husks), are suspended in water and applied to the rice bodies. The seeds were uniformly inoculated by spraying and placed in a constant temperature and humidity box at a temperature of 27°C and a humidity of 95% or higher to induce disease. On the fourth day after inoculation, the number of lesions per leaf was determined, and the control value was calculated according to the following formula. On the other hand, sodium bicarbonate and various polyglycerol fatty acid esters were used alone as control agents and treated in the same manner, the degree of onset of each disease was examined, and the control value was calculated. Control value (%) = (1 - number of lesions in sprayed area/number of lesions in non-sprayed area) x 100 The results are shown in Table 3.

【表】【table】

【表】 試驗例 4 (かんきつ黒点病害防除試驗) 温州ミカンの約3年生実生苗の新梢(6寸鉢2
〜4本植)を供試植物とし、調査時に新梢を基部
から切断して混合肥料を10〜20粒施し、その後約
2〜3週間後に新梢を再び供試する。実施例1〜
3に準じて調製した水和剤を所定濃度に希釈した
薬剤を、2鉢当り40mlずつ均一に噴霧散布する。
次いで試驗管中のかんきつ黒点病原菌培養枝に殺
菌水を流し込み、柄胞子懸濁液とし、これを150
培顕微鏡下1視野中、約200個に調製し、噴霧接
種する。接種後は、接種箱内で約3日間湿室に保
ち、十分感染後に温室に移動する。 接種後、約2〜3週間を経た新梢の全葉につい
て病斑1〜50個(1)、51〜150個(2)、151個以上(3)、
無発病(0)とに分けて調査し、次式により発病
度並びに防除価(%)を算出した。 発病度=1Xn1+2Xn2+3Xn3/3XN×100 (但し、n1、n2、n3はそれぞれ発病程度(1)、(2)、
(3)の葉数、Nは総葉数を示す。) 防除価(%)=(1−処理区の発病度/無処理区の発病
度)×100 一方、対照薬剤として炭酸水素ナトリウム及び
各種ポリグリセロール脂肪酸エステルをそれぞれ
単独で用いて同様に処理し、発病の程度を調べ、
防除価を算出した。 これらの結果を第4表に示す。
[Table] Trial example 4 (Citrus black spot disease control trial) New shoots of approximately 3-year-old unshiu mandarin seedlings (2 in 6-inch pots)
~4 plants) are used as test plants, and at the time of investigation, the new shoots are cut off from the base and 10 to 20 grains of mixed fertilizer are applied, and the new shoots are then tested again about 2 to 3 weeks later. Example 1~
A hydrating powder prepared according to step 3 was diluted to a predetermined concentration, and 40 ml of the drug was evenly sprayed per two pots.
Next, sterilized water was poured into the citrus blackspot pathogen culture branch in the test tube to obtain a stalk spore suspension, and this was
Prepare approximately 200 cells per field of view under a culture microscope and inoculate them by spraying. After inoculation, the inoculation box is kept in a moist room for about 3 days, and after sufficient infection, it is moved to a greenhouse. 1 to 50 lesions (1), 51 to 150 lesions (2), 151 or more lesions (3) on all leaves of new shoots approximately 2 to 3 weeks after inoculation,
The disease-free disease (0) and disease-free disease were investigated separately, and the disease severity and control value (%) were calculated using the following formula. Disease severity = 1Xn 1 + 2Xn 2 + 3Xn 3 / 3XN x 100 (However, n 1 , n 2 , n 3 are disease severity (1), (2), respectively)
(3) Number of leaves, N indicates the total number of leaves. ) Control value (%) = (1 - severity of disease in treated area / severity of disease in untreated area) x 100 On the other hand, sodium bicarbonate and various polyglycerol fatty acid esters were treated in the same way as control agents, respectively, and Check the severity of the disease,
The control value was calculated. These results are shown in Table 4.

【表】 試驗例 5 (キユウリ炭疽病害防除試驗) ポツトに播種して16〜17日間生育したキユウリ
幼苗(品種:相模半白)に、実施例1〜3で調整
した水和剤を所定濃度に水で希釈して、スプレー
ガンを用いて10ポツト当り40ml散布し、散布薬液
の乾燥後、これにキユウリ炭疽病菌
(Colletotrichum laqenarium)を接種した。接
種は、ジヤガイモ寒天培地上で生育したキユウリ
炭疽病菌胞子を胞子濃度が1視野(顕微鏡倍率:
150)中約200個の懸濁液にして接種箱内で噴霧す
る方法で行つた。次いで、これを湿度100%の接
種箱内に24時間放置してから、自然光の温室に移
し、3〜4日経過後、病斑数を調査し、次式によ
り防除価を算出した。なお、各処理区の試驗は10
連で行つた。 防除価(%)= 無処理区の病斑数−処理区の病斑数/無処理区の病斑
数×100 一方、対照薬剤として炭酸水素ナトリウム及び
各種ポリグリセロール脂肪酸エステルを用いて同
様の処理を行い、防除価を算出した。 この結果を第5表に示す。
[Table] Test Example 5 (Test for controlling anthracnose disease in cucumbers) Young cucumber seedlings (variety: Sagami Hanshiro), which were sown in pots and grown for 16 to 17 days, were treated with the hydrating agent prepared in Examples 1 to 3 at a prescribed concentration. The solution was diluted with water and sprayed at 40 ml per 10 pots using a spray gun. After drying, the solution was inoculated with Colletotrichum laqenarium. For inoculation, spores of cucumber anthracnose grown on a potato agar medium were collected in one field of view (microscopic magnification:
150) was made into a suspension of approximately 200 particles and sprayed in an inoculation box. Next, this was left in an inoculation box with 100% humidity for 24 hours, and then transferred to a greenhouse with natural light. After 3 to 4 days, the number of lesions was investigated, and the control value was calculated using the following formula. In addition, there were 10 trials in each treatment area.
We went together. Control value (%) = Number of lesions in untreated area - Number of lesions in treated area / Number of lesions in untreated area × 100 On the other hand, similar treatments were performed using sodium bicarbonate and various polyglycerol fatty acid esters as control agents. The control value was calculated. The results are shown in Table 5.

【表】 試驗例 6 (トマトモザイクウイルス(TMV)病害防除
試驗 (試驗方法) 1 供試植物 直径6.5cmの穴あきコツプに1本植とした、
播種後5週間空調温室で栽培したトマト苗を供
試した。土はクレハソイルを用い、空調温室の
設定条件は、昼間最高温度28℃、夜間最低温度
20℃、湿度60%、日照時間は12時間となるよう
に朝夕及び曇雨天時には水銀灯で補充した。 2 薬剤散布 実施例1〜3に従つて調製した水和剤に水を
加えて所定濃度の薬液に稀釈する。使用前に展
着剤を1滴加え、植物をターンテーブル上で回
転させながらスプレーガンで散布した。散布時
のコンプレツサーのゲージ圧力は2Kg/cm2であ
る。 3 接種 薬液が風乾後、TMVを吹付接種した。接種
条件は、罹病トマト葉1g(生重)を磨砕し、
蒸留水を加え、ガーゼで過後、蒸留水を加え
て1とする。このウイルス液に500メツシユ
のカーボランダム10gを加えてスターラーで撹
拌しながら接種する。この時のスプレーガン噴
霧口よりトマトの芯葉までの距離は20cm、コン
プレツサーのゲージ圧力4Kg/cm2、接種時間
0.5秒である。 4 発病及び調査 接種した植物はフアンジトロン内で生育さ
せ、10〜14日後に発病の有無を調査した。フア
ンジトロンの設定条件は温度28℃、湿度70%で
12時間陽光ランプによる人工照明を行つた。 なお、発病率及び防除価の定義は次の如くで
ある。 発病率は、各供試化合物について供試植物体
中の発病株を調べた。用いた供試株数は100株
である。 発病率=発病株数/供試株数×100 防除価(%)=100−発病率 この結果を第6表に示す。
[Table] Test example 6 (Tomato mosaic virus (TMV) disease control test (test method) 1 Test plant One plant was planted in a pot with a hole of 6.5 cm in diameter.
Tomato seedlings grown in an air-conditioned greenhouse for 5 weeks after sowing were used as test samples. The soil is Kureha soil, and the conditions for the air-conditioned greenhouse are a maximum daytime temperature of 28℃ and a minimum nighttime temperature.
The temperature was 20°C, the humidity was 60%, and the sunlight was 12 hours long, with mercury lamps being used in the morning and evening and during cloudy and rainy days. 2. Chemical Spraying Water is added to the wettable powders prepared according to Examples 1 to 3 to dilute the chemical solution to a predetermined concentration. Before use, one drop of spreading agent was added and sprayed with a spray gun while the plants were rotated on a turntable. The gauge pressure of the compressor during spraying is 2 Kg/cm 2 . 3. Inoculation After the chemical solution was air-dried, TMV was spray inoculated. The inoculation conditions were to grind 1 g (fresh weight) of diseased tomato leaves,
Add distilled water, pass through gauze, and add distilled water to make 1. Add 10 g of 500 mesh of carborundum to this virus solution and inoculate while stirring with a stirrer. At this time, the distance from the spray gun nozzle to the core leaf of the tomato was 20 cm, the compressor gauge pressure was 4 Kg/cm 2 , and the inoculation time was 20 cm.
It is 0.5 seconds. 4. Disease onset and investigation The inoculated plants were grown in a fanzitron, and the presence or absence of disease onset was investigated 10 to 14 days later. The setting conditions for Fungitron are a temperature of 28℃ and a humidity of 70%.
Artificial lighting was provided using a 12-hour sunlight lamp. In addition, the definitions of attack rate and control value are as follows. The disease attack rate was determined by examining the diseased strains in the test plants for each test compound. The number of test stocks used was 100. Disease attack rate = Number of diseased plants/Number of test plants x 100 Control value (%) = 100 - disease attack rate The results are shown in Table 6.

〔試験結果〕〔Test results〕

次式を用いて防除価(%)を算出した。 防除価(%)=1−処理区の測定値(計算値)/無処理
区の測定値(計算値) 一方、対照薬剤として炭酸水素ナトリウム及び
各種ポリグリセロール脂肪酸エステルを用いて同
様の処理を行い、防除価を算出した。 この結果を第7表に示す。
Control value (%) was calculated using the following formula. Control value (%) = 1 - Measured value of treated area (calculated value) / Measured value of untreated area (calculated value) On the other hand, similar treatments were performed using sodium bicarbonate and various polyglycerol fatty acid esters as control agents. , the control value was calculated. The results are shown in Table 7.

〔考察〕[Consideration]

以上の試験例で明らかなように、各種植物病
害、果実貯蔵病害及び植物ウイルス病害に対し
て、各種ポリグリセロール脂肪酸エステル及び炭
酸水素ナトリウムを各単独で用いた場合、各種ポ
リグリセロール脂肪酸エステル単独では防除価は
極めて低く、炭酸水素ナトリウム単独では防除価
は高くとも60%台で、しかも病害が激発状態にな
る程、防除価が相対的に低下する傾向を示すのに
対して、本発明組成物の防除効果は極めて安定し
ており、病害の激発状態において100%近い防除
(治療及び予防)価が持続的に再現性よく得られ
ること及び従来の殺菌剤が植物ウイルス病害に対
して殆んど無効であるのに対してかび及び細菌性
植物病害と同等に顕著な防除効果が得られたこと
は注目に値するものである。
As is clear from the above test examples, when various polyglycerol fatty acid esters and sodium hydrogen carbonate are used alone against various plant diseases, fruit storage diseases, and plant virus diseases, the various polyglycerol fatty acid esters alone do not control the diseases. The control value of sodium bicarbonate alone is in the 60% range at most, and the control value tends to decrease relatively as the disease becomes more severe, whereas the control value of the composition of the present invention is extremely low. The control effect is extremely stable, and nearly 100% control (treatment and prevention) value can be obtained continuously and reproducibly even in conditions of severe disease outbreaks, and conventional fungicides are almost ineffective against plant virus diseases. However, it is noteworthy that the same remarkable effect on controlling fungal and bacterial plant diseases was obtained.

Claims (1)

【特許請求の範囲】[Claims] 1 炭酸水素ナトリウムとポリグリセロール脂肪
酸エステルの1種又は2種以上とを有効成分とし
て含有することを特徴とする農園芸用殺菌剤及び
植物ウイルス病害防除剤組成物。
1. An agricultural and horticultural fungicide and plant virus disease control agent composition containing one or more of sodium bicarbonate and polyglycerol fatty acid ester as active ingredients.
JP11812679A 1979-09-14 1979-09-14 Agricultural and horticultural germicide and plant blight control agent composition Granted JPS5643207A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11812679A JPS5643207A (en) 1979-09-14 1979-09-14 Agricultural and horticultural germicide and plant blight control agent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11812679A JPS5643207A (en) 1979-09-14 1979-09-14 Agricultural and horticultural germicide and plant blight control agent composition

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Publication Number Publication Date
JPS5643207A JPS5643207A (en) 1981-04-21
JPS6328043B2 true JPS6328043B2 (en) 1988-06-07

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ID=14728674

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Country Link
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JPS58146470U (en) * 1982-03-29 1983-10-01 宮城島 玄也 fishing line reel clutch
DK244685D0 (en) * 1985-05-31 1985-05-31 Nexus Aps POLYGLYCEROLEMULGATOR
JPH02188504A (en) * 1989-01-17 1990-07-24 Osaka Kasei Kk Self-adsorbable antimicrobial agent and fiber product treated with the same antimicrobial agent
US6103768A (en) * 1991-05-01 2000-08-15 Mycogen Corporation Fatty acid based compositions and methods for the control of plant infections and pests
CA2081652C (en) * 1991-10-31 2002-09-10 Yuichi Hioki Agricultural chemical composition
WO1996028022A2 (en) * 1995-03-08 1996-09-19 Mycogen Corporation Fatty acid based compositions and methods for the control of plant infections and pests
EP0903080A4 (en) * 1996-04-15 2003-01-08 New Japan Chem Co Ltd Red tide eliminating composition and method for getting rid of red tide
WO2001008481A1 (en) * 1999-07-30 2001-02-08 Clariant Gmbh Pesticide preparations containing polyglycerin or polyglycerin derivatives
JP2001172104A (en) * 1999-12-14 2001-06-26 Yushiro Chem Ind Co Ltd Spreader, agrochemical composition with the same added thereto, and method for spraying agrochemical
FR2842706B1 (en) * 2002-07-26 2006-04-14 Novance METHOD FOR CONTROLLING PROPAGATION OF NON-PERSISTENT VIRUSES, COMPOSITION AND USE
JP2013231003A (en) * 2012-04-27 2013-11-14 Institute Of Physical & Chemical Research Control agent for black sigatoka disease

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5081856A (en) * 1973-11-15 1975-07-02
JPS5163932A (en) * 1974-11-27 1976-06-02 Rikagaku Kenkyusho Noengeiyosatsukin oyobi chozobyogaibojozai
JPS545525A (en) * 1977-06-15 1979-01-17 Toshiba Corp Transformer for network
JPS5437827A (en) * 1977-08-31 1979-03-20 Rikagaku Kenkyusho Bactericidal composition for agricultural and horticultural uses effective also against fruit pests during storage

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5081856A (en) * 1973-11-15 1975-07-02
JPS5163932A (en) * 1974-11-27 1976-06-02 Rikagaku Kenkyusho Noengeiyosatsukin oyobi chozobyogaibojozai
JPS545525A (en) * 1977-06-15 1979-01-17 Toshiba Corp Transformer for network
JPS5437827A (en) * 1977-08-31 1979-03-20 Rikagaku Kenkyusho Bactericidal composition for agricultural and horticultural uses effective also against fruit pests during storage

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JPS5643207A (en) 1981-04-21

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