JPH0751489B2 - Agrochemical composition consisting of natural products - Google Patents

Agrochemical composition consisting of natural products

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Publication number
JPH0751489B2
JPH0751489B2 JP2295092A JP2295092A JPH0751489B2 JP H0751489 B2 JPH0751489 B2 JP H0751489B2 JP 2295092 A JP2295092 A JP 2295092A JP 2295092 A JP2295092 A JP 2295092A JP H0751489 B2 JPH0751489 B2 JP H0751489B2
Authority
JP
Japan
Prior art keywords
wood vinegar
lysophospholipid
fatty acid
weight
solution
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 - Lifetime
Application number
JP2295092A
Other languages
Japanese (ja)
Other versions
JPH06279221A (en
Inventor
哲 藤田
鍾徳 天野
Original Assignee
株式会社ビー・エヌ有機農法研究所
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Priority to JP2295092A priority Critical patent/JPH0751489B2/en
Publication of JPH06279221A publication Critical patent/JPH06279221A/en
Publication of JPH0751489B2 publication Critical patent/JPH0751489B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、農作物、園芸植物、植
木などの駆虫、生育促進に有効な天然系農薬組成物に関
する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a natural agrochemical composition which is effective for deworming and promoting the growth of agricultural crops, horticultural plants, plants and the like.

【0002】[0002]

【従来の技術】木酢液は木炭製造など、木材の乾溜時に
発生する気体を冷却して得られる酸性の液体で、古く
は、酢酸やアセトンの原料として、また、木材や食品の
防腐剤、くん液、し尿や家畜の糞尿の消臭剤などの用途
に用いられてきた。最近は、有機農法の普及や、減農薬
農業、化学合成された農薬の忌避の傾向から、生体への
安全性の高い木酢液が特に近年注目され、土壌消毒、厩
・堆肥に添加する肥料製造、雑草防除、植物成長促進、
害虫忌避など、農業用の用途が増加している(特公昭6
3−24964号公報、山林誌,1978年,28頁、
木材学雑誌,35卷,564頁、及び1021頁参
照)。
2. Description of the Related Art Wood vinegar is an acidic liquid obtained by cooling the gas generated during the dry distillation of wood, such as in the production of charcoal. In the old days, it was used as a raw material for acetic acid and acetone. It has been used as a deodorant for liquid, human waste and livestock manure. Recently, due to the widespread use of organic farming methods, reduced pesticide agriculture, and the tendency to avoid chemically synthesized pesticides, wood vinegar, which is highly safe for living organisms, has been receiving particular attention in recent years. , Weed control, plant growth promotion,
Agricultural applications such as pest repellent are increasing (Japanese Patent Publication 6)
3-24964, Yamabayashi, 1978, p. 28,
Lumber magazine, 35, 564, and 1021).

【0003】[0003]

【発明が解決しようとする課題】木酢液は、その安全性
の点から、有機農法野菜、家庭園芸、庭園用樹木や芝生
などへの利用の増加が大きい。木酢液は、これらの農業
用の用途に、通常、水で50−1000倍程度に希釈し
て用いられるが、効果が遅く、特に、害虫忌避の点では
十分な効果が得られない欠点があった。この点を改良す
るには、木酢液に合成の殺虫剤を混合するなどの方法が
行われたり、また別途に殺虫剤の散布を行う必要があっ
た。
From the viewpoint of safety, the use of wood vinegar is greatly increased in organic farm vegetables, home gardening, garden trees and lawns, and the like. The wood vinegar is usually used after diluting it with water about 50 to 1000 times for these agricultural uses, but its effect is slow, and there is a drawback that a sufficient effect cannot be obtained particularly in terms of pest repellent. It was In order to improve this point, a method of mixing a synthetic pesticide with a wood vinegar solution or the like, or it was necessary to separately spray the pesticide.

【0004】[0004]

【課題を解決するための手段及び作用】本発明者らは、
前記の木酢液の性能を向上するために、種々研究の結
果、木酢液にリゾリン脂質を混合することにより、木酢
液の有する前記の農薬的な効果を飛躍的に増強すること
ができた。
Means and Actions for Solving the Problems The present inventors have
As a result of various studies in order to improve the performance of the wood vinegar, it was possible to dramatically enhance the above-mentioned pesticidal effect of the wood vinegar by mixing lysophospholipid with the wood vinegar.

【0005】すなわち、本発明の第一の天然系農薬組成
物は、木酢液とリゾリン脂質からなり、また本発明の第
2の天然系農薬組成物は木酢液とリゾリン脂質及び脂肪
酸を含むことを要旨とする。本発明でいう農薬とは、そ
の奏する作用効果は通常の農薬が有する作業効果とほぼ
同程度を示し、例えば病気の予防、駆虫、殺虫、生育促
進等の如きをいう。
That is, the first natural agrochemical composition of the present invention comprises wood vinegar and lysophospholipid, and the second natural agrochemical composition of the present invention contains wood vinegar, lysophospholipid and fatty acid. Use as a summary. The pesticide referred to in the present invention is
The action and effect exhibited by are similar to those of ordinary pesticides, and include, for example, disease prevention, anthelmintic, insecticidal, and growth promoting.

【0006】本発明の天然系農薬組成物は、木酢液/リ
ゾリン脂質の重量比が20:80−97:3であるか、
及び木酢液/リゾリン脂質の重量比が20:80−9
7:3であり、さらにリゾリン脂質に対して100重量
%以下の脂肪酸を含むものであることが特に好ましい。
The natural agricultural chemical composition of the present invention has a weight ratio of wood vinegar / lysophospholipid of 20: 80-97: 3,
And the weight ratio of wood vinegar / lysophospholipid is 20: 80-9.
It is 7: 3 and particularly preferably contains 100% by weight or less of a fatty acid with respect to the lysophospholipid.

【0007】さらに本発明は、使用するリゾリン脂質が
大豆リゾリン脂質であり、脂肪酸が不飽和脂肪酸及びま
たは炭素原子数8−14の中鎖脂肪酸であることを特徴
とする天然系農薬組成物に関する。
The present invention further relates to a natural agricultural chemical composition characterized in that the lysophospholipid used is soybean lysophospholipid and the fatty acid is unsaturated fatty acid and / or medium chain fatty acid having 8 to 14 carbon atoms.

【0008】本発明における木酢液とは、一般には黒炭
や白炭などの木炭の製造に際して得られるもの、また、
おがくず、廃木材、樹皮、バーク、籾殻などの乾溜によ
って得られるものが用いられる。炭焼きや、木材等の乾
溜によって発生する気体を冷却して得られる液体を長時
間靜置して、沈降するタール分を分離したものが粗木酢
液である。粗木酢液はそのままでも用いることができる
が、さらに濾過や遠心分離などによって不溶物を除いた
ものはさらに適する。また粗木酢液を常圧もしくは減圧
下で蒸留したものも用いることができる。
The wood vinegar in the present invention is generally obtained in the production of charcoal such as black charcoal and white charcoal, and
Sawdust, waste wood, bark, bark, chaff, etc. obtained by dry distillation are used. A crude wood vinegar solution is a solution obtained by placing a liquid obtained by cooling the gas generated by charcoal burning or dry distillation of wood etc. for a long time and separating the precipitated tar content. The crude wood vinegar can be used as it is, but it is more suitable if the insoluble matter is removed by filtration or centrifugation. Moreover, what distilled the crude wood vinegar liquid under normal pressure or reduced pressure can also be used.

【0009】木酢液の成分は原料、製造方法、特に温度
条件によってある程度異なるが、通常は、比重1.01
−1.04、水分80−90%、pH2−4で、有機物
として、酢酸を主とする有機酸類、メタノールなどのア
ルコール類、アセトンなどの中性有機物、フェノール類
など、殆ど無数といえる成分を含有している(木材炭化
成分多用途利用技術研究組合発行「木炭と木酢液の新用
途開発研究成果集」1990年、297頁参照)。本発
明においては、これらの木酢液のいずれをも用いること
ができる。また、通常の木酢液に苛性ソーダなどのアル
カリ性成分を加えて中和したものも用いることができ
る。
The components of the wood vinegar solution vary to some extent depending on the raw materials, the manufacturing method, especially the temperature conditions, but usually the specific gravity is 1.01.
-1.04, water content 80-90%, pH 2-4, as organic substances, organic acids mainly acetic acid, alcohols such as methanol, neutral organic substances such as acetone, and phenols, etc. Contained (Refer to “Collection of Research Results on New Uses of Charcoal and Wood Vinegar”, p. 297, published by Research Association for Multi-Use Technology for Carbonized Wood). In the present invention, any of these wood vinegar solutions can be used. In addition, it is also possible to use an ordinary wood vinegar solution neutralized by adding an alkaline component such as caustic soda.

【0010】なお木酢液の持つ土壌消毒、微生物の増殖
促進、雑草防除、植物成長促進、植物の耐病性増加、害
虫忌避などの作用が、それぞれ、どの成分に起因し、ど
の様な機作で起こるかは現在においてもなお不明であ
る。
The action of the wood vinegar solution such as soil disinfection, microbial growth promotion, weed control, plant growth promotion, plant disease resistance increase, pest repelling, etc. is caused by each component and by what mechanism It still remains unclear what will happen.

【0011】本発明に用いるリゾリン脂質とは、大豆や
菜種などの植物種子由来のリン脂質や卵黄リン脂質を、
ホスフォリパーゼAによって脱アシル化した、モノアシ
ル体のリン脂質であって、通常は膵臓由来のホスフォリ
パーゼA-2で処理されたものが用いられる。特に大豆油
の精製時に副生する大豆リン脂質(大豆レシチン)から
作る大豆リゾリン脂質は安価であり、本発明の原料に適
する。これらのリゾリン脂質は、リゾホスファチジルコ
リン、リゾホスファチジルエタノールアミン、リゾホス
ファチジルイノシトール、リゾホスファチジン酸などの
モノアシルグリセロリン脂質を含む。またこれらの混合
物から含水アルコール処理などによってリゾホスファチ
ジルコリンの含有量を増加させたものも適する。化学合
成されたリゾリン脂質も同様に用いることができる。
The lysophospholipids used in the present invention include phospholipids derived from plant seeds such as soybeans and rapeseed and egg yolk phospholipids,
A monoacyl phospholipid deacylated by phospholipase A, which is usually treated with pancreatic phospholipase A-2, is used. In particular, soybean lysophospholipid made from soybean phospholipid (soybean lecithin) produced as a by-product at the time of refining soybean oil is inexpensive and is suitable as a raw material of the present invention. These lysophospholipids include monoacylglycerophospholipids such as lysophosphatidylcholine, lysophosphatidylethanolamine, lysophosphatidylinositol, lysophosphatidic acid. Further, those obtained by increasing the content of lysophosphatidylcholine from these mixtures by treatment with hydrous alcohol are also suitable. A chemically synthesized lysophospholipid can be used as well.

【0012】前記酵素処理によっては全てのリン脂質を
リゾリン脂質にすることは困難で、ジアシル体リン脂質
が残存するが、リゾリン脂質の量はリン脂質全体の50
重量%以上であることが本発明の原料に適する。このよ
うなものであれば、リゾリン脂質が、例えば、通常の油
分を含むペースト状の大豆リン脂質をホスフォリパーゼ
A-2で処理した後、リゾリン脂質の含水ペーストを遠心
分離して、油分と脂肪酸を除いたものでもよい。また、
ホスフォリパーゼA-2処理の後、脂肪酸をある程度中和
し、油分などを含んだまま製品化したものであってもよ
い。更に、ホスフォリパーゼA-2処理後、アセトンなど
の溶剤によって精製し、油脂及び発生した脂肪酸を除い
たものでもよい。いずれの場合にも、木酢液に対するリ
ゾリン脂質の添加量はその絶対量で計算する。
It is difficult to convert all phospholipids into lysophospholipids by the above enzyme treatment, and diacyl phospholipids remain, but the amount of lysophospholipids is 50% of the total phospholipids.
It is suitable for the raw material of the present invention that the content is at least wt%. If this is the case, the lysophospholipid is, for example, a paste-like soybean phospholipid containing an ordinary oil component is treated with phospholipase A-2, and then the lysophospholipid-containing paste is centrifuged to obtain an oil component. It may be one without fatty acids. Also,
After the treatment with phospholipase A-2, the fatty acid may be neutralized to some extent, and the product may be produced with the oil content contained. Furthermore, after the treatment with phospholipase A-2, the product may be purified with a solvent such as acetone to remove fats and oils and generated fatty acids. In either case, the amount of lysophospholipid added to the wood vinegar is calculated as the absolute amount.

【0013】本発明に使用する不飽和脂肪酸は、リノー
ル酸、リノレン酸、オレイン酸、アラキドン酸、エイコ
サペンタエン酸、ドコサヘキサエン酸、などの脂肪酸及
びこれらの混合物であって、パルミチン酸、ステアリン
酸などの飽和脂肪酸が存在していてもよい。この点では
大豆油などの植物油の脂肪酸もまた適する。
The unsaturated fatty acid used in the present invention is a fatty acid such as linoleic acid, linolenic acid, oleic acid, arachidonic acid, eicosapentaenoic acid, docosahexaenoic acid and a mixture thereof, such as palmitic acid and stearic acid. Saturated fatty acids may be present. In this respect, the fatty acids of vegetable oils such as soybean oil are also suitable.

【0014】本発明に使用する中鎖脂肪酸とは、カプリ
ン酸、カプリル酸、ラウリン酸、ミリスチン酸、または
これらの混合物であって、少量の他の脂肪酸が混在して
もよい。従って、ヤシ油、パーム核油などの脂肪酸もま
た適する。
The medium-chain fatty acid used in the present invention is capric acid, caprylic acid, lauric acid, myristic acid, or a mixture thereof, and a small amount of other fatty acid may be mixed. Therefore, fatty acids such as coconut oil and palm kernel oil are also suitable.

【0015】本発明の第1は、前記木酢液に対して、リ
ゾリン脂質をその絶対量で、重量比率で、20:80−
97:3の範囲で加える。混合は加熱下で行うのがよい
が、木酢液中の揮発性成分の損失を避けるために、80
℃以下で行うことが好ましい。混合の時期は、予め両者
を混合しておき、使用に当たって希釈して用いてもよい
し、また使用の直前に両者を混合してから希釈して用い
てもよい。更に、希釈した木酢液とリゾリン脂質水溶液
を混合して用いてもよい。組成物中の木酢液の量が20
重量%以下か、リゾリン脂質の量が3重量%以下では組
成物の効力が不十分である。なお木酢液/リゾリン脂質
の比は通常1以上であればよいが、リゾリン脂質の重量
比がそれ以上になっても上記範囲内であれば、目的に応
じて希釈率を変えて用いることが出来る。
The first aspect of the present invention is that the absolute amount of lysophospholipid in the wood vinegar solution is 20: 80-in terms of a weight ratio.
Add in the range of 97: 3. Mixing should be carried out under heating, but to avoid loss of volatile components in the wood vinegar, 80%
It is preferably carried out at a temperature of not higher than 0 ° C. At the time of mixing, both may be mixed in advance and diluted before use, or both may be mixed immediately before use and then diluted. Further, a diluted wood vinegar solution and an aqueous lysophospholipid solution may be mixed and used. The amount of wood vinegar in the composition is 20
If the amount of lysophospholipid is less than 3% by weight or less, the efficacy of the composition is insufficient. The ratio of wood vinegar / lysophospholipid is usually 1 or more, but even if the weight ratio of lysophospholipid is more than that, if the ratio is within the above range, the dilution ratio can be changed according to the purpose. .

【0016】本発明の第2では、木酢液とリゾリン脂質
を重量比で20:80−97:3の範囲で混合し、更に
脂肪酸をリゾリン脂質100部に対して重量比で100
部以下を加える。混合は第1の場合と同様に均一な溶液
が得られれば、どの様な方法であってもよいが、この場
合は予めリゾリン脂質の水溶液を加熱下に作っておき、
それに脂肪酸を溶解した後、木酢液と混合すると容易に
組成物を得ることができる。
In the second aspect of the present invention, wood vinegar and lysophospholipid are mixed in a weight ratio of 20:80 to 97: 3, and fatty acid is added to 100 parts of lysophospholipid in a weight ratio of 100.
Add the following parts. Mixing may be performed by any method as long as a uniform solution can be obtained as in the first case. In this case, an aqueous solution of lysophospholipid is prepared in advance by heating,
The composition can be easily obtained by dissolving the fatty acid therein and then mixing it with wood vinegar.

【0017】三者の混合の時期と希釈の方法は任意に選
定できる。組成物中の木酢液の量が20重量%以下か、
リゾリン脂質の量が3重量%以下では組成物の効果が不
十分であり、脂肪酸の量がリゾリン脂質の量を越えると
脂肪酸が溶解されず、析出するので好ましくない。木酢
液/リゾリン脂質/脂肪酸の組成物では、木酢液/リゾ
リン脂質の組成物に比べてリゾリン脂質の量が少量でも
前者と同等の効果が得られることが多い。また木酢液/
(リゾリン脂質+脂肪酸)の比は通常1以上であればよ
いが、リゾリン脂質と脂肪酸の合計の重量比がそれ以上
になっても上記範囲内であれば、目的に応じて希釈率を
変えて用いることが出来る。
The mixing timing and the dilution method of the three can be arbitrarily selected. If the amount of wood vinegar in the composition is 20% by weight or less,
When the amount of lysophospholipid is 3% by weight or less, the effect of the composition is insufficient, and when the amount of fatty acid exceeds the amount of lysophospholipid, the fatty acid is not dissolved and is precipitated, which is not preferable. In the composition of wood vinegar / lysophospholipid / fatty acid, the same effect as the former is often obtained even when the amount of lysophospholipid is small compared to the composition of wood vinegar / lysophospholipid. Also wood vinegar /
The ratio of (lysophospholipid + fatty acid) may be usually 1 or more, but if the total weight ratio of lysophospholipid and fatty acid is more than the above range and the ratio is within the above range, the dilution rate may be changed according to the purpose. Can be used.

【0018】木酢液そのものは農薬ではないので、急速
な作用は現れない。しかし、木酢液を通常の農薬や化学
肥料などと併用すると、それらの作用を強化する働きが
大きいので、減農薬剤としての利用も拡大している。従
って、木酢液のみでは、全くの無農薬農法を実現するこ
とは困難であったし、特に害虫忌避作用は不十分であっ
た。しかるに本発明による組成物は驚くべきことには、
極めて顕著な害虫忌避作用と共に、殺虫効果を有した。
Since the wood vinegar solution itself is not a pesticide, it does not show a rapid action. However, when wood vinegar is used in combination with ordinary pesticides and chemical fertilizers, it has a great effect of strengthening those effects, and therefore its use as a pesticide-reducing agent is expanding. Therefore, it was difficult to realize a completely pesticide-free farming method using only wood vinegar, and the pest repellent effect was particularly insufficient. However, the composition according to the invention is surprisingly
It had a pesticidal effect as well as a very pronounced pest repellent effect.

【0019】リゾリン脂質の浸透作用は工業用の界面活
性剤に比べて強くない。ある種のリゾリン脂質/脂肪酸
混合物に、強い浸透、湿潤、展着効果のあることは公知
である(特開平2−203928)。しかし、本発明の
組成物の効果は、前記リゾリン脂質/脂肪酸混合物と同
程度の浸透、湿潤、展着効果のある工業的界面活性剤、
ポリオキシエチレンノニルフェノールエーテルを、リゾ
リン脂質またはリゾリン脂質/脂肪酸混合物の代わりに
用いて、木酢液に加えても、それを得ることができな
い。
The penetrating action of lysophospholipids is not as strong as that of industrial surfactants. It is known that certain lysophospholipid / fatty acid mixtures have strong penetrating, wetting and spreading effects (JP-A-2-203928). However, the effect of the composition of the present invention is that an industrial surfactant having the same penetration, wetting and spreading effects as the lysophospholipid / fatty acid mixture,
If polyoxyethylene nonylphenol ether is used instead of lysophospholipid or lysophospholipid / fatty acid mixture and added to wood vinegar, it cannot be obtained.

【0020】本発明の天然系農薬組成物には、本発明の
目的を損なわない範囲で、界面活性剤、脂肪酸モノグリ
セリド、カゼインなどの蛋白質、蛋白質の酵素分解物、
繊維素グリコール酸ソーダなどの増粘剤、木炭の微粉
末、キトサンなどの添加物を加えることができ、また、
ニンニク、ヨモギ、ドクダミなどの防虫、殺菌性を有す
る天然物の抽出物を加えることができる。
The natural agrochemical composition of the present invention contains a protein such as a surfactant, a fatty acid monoglyceride, and casein, an enzymatic decomposition product of the protein, within a range that does not impair the object of the present invention.
Thickeners such as sodium fiber glycolate, charcoal fine powder, and additives such as chitosan can be added.
It is possible to add an extract of natural products having insecticidal and bactericidal properties such as garlic, mugwort and Dokudami.

【0021】[0021]

【実施例】以下に実施例と実験例を挙げて本発明の効果
を検証するが、本発明はそれらに限定されない。以下
に、この実施例中で使用した木酢液、及びリゾリン脂質
について示す。
EXAMPLES The effects of the present invention will be verified below with reference to Examples and Experimental Examples, but the present invention is not limited thereto. The wood vinegar solution and lysophospholipid used in this example are shown below.

【0022】<木酢液> ・ホートク物産(株)製、ハイモクサン、本品は比重
1.018、pH3.2の木酢液であった。 ・(株)信濃有機製の中和木酢液、本品は酸性を中和に
よって緩和したもので、比重1.021、pH5.9の
木酢液であった。
<Wood Vinegar> High moxan, manufactured by Hortoku Bussan Co., Ltd., had a specific gravity of 1.018 and a pH of 3.2. -Neutralized wood vinegar made by Shinano Organic Co., Ltd. This product was prepared by neutralizing acidity and had a specific gravity of 1.021 and a pH of 5.9.

【0023】<リゾリン脂質> ・味の素の製含油大豆リン脂質1kgに、膵ホスフォリ
パーゼA-2(ノボ社製レシターゼ10−L)2gを含む
水道水200gを加えて攪拌し、60℃に一日靜置し、
遠心分離によって上部に分離した油層を除いた。沈降し
た水分を含む大豆リゾリン脂質を集め、均一に混合した
ものを酵素処理脂質Aとした。酵素処理脂質Aはアセト
ン不溶分(リン脂質)53重量%と脂肪酸11重量%
と、他は油脂、水からなり、またアセトン不溶分はTL
C−FID法(ヤトロン社製イヤトロスキャンTH−1
0)による分析の結果、リゾリン脂質を重量比で84%
含んでいた。従って酵素処理脂質A中には純分で45重
量%のリゾリン脂質を含む。
<Rhizophospholipid> 200 g of tap water containing 2 g of pancreatic phospholipase A-2 (lecitase 10-L manufactured by Novo Co.) was added to 1 kg of oil-containing soybean phospholipid manufactured by Ajinomoto, and stirred at 60 ° C. Place in the sun
The oil layer separated on the top was removed by centrifugation. The soybean lysophospholipid containing the precipitated water was collected and uniformly mixed to obtain enzyme-treated lipid A. Enzyme-treated lipid A is acetone insoluble matter (phospholipid) 53 wt% and fatty acid 11 wt%
And the others consist of oil and fat, and acetone insoluble matter is TL
C-FID method (Yatroscan TH-1 manufactured by Yatron)
0) analysis showed that lysophospholipid was 84% by weight.
Included. Accordingly, the enzyme-treated lipid A contains 45% by weight of pure lysophospholipid.

【0024】・酵素処理脂質Aと同様に処理して得た反
応終了物600gにアセトン1kgを加えて、50℃に
加熱攪拌後に15℃まで冷却し遠心分離して、アセトン
不溶分を得、減圧下にアセトンを溜去してリゾリン脂質
を得た。これを酵素処理脂質Bとした。酵素処理脂質B
は固形分97重量%、リゾリン脂質83重量%を含ん
だ。
1 kg of acetone was added to 600 g of the reaction product obtained by treating in the same manner as the enzyme-treated lipid A, heated and stirred at 50 ° C., cooled to 15 ° C., and centrifuged to obtain an acetone-insoluble matter, and decompression Acetone was distilled off underneath to obtain lysophospholipid. This was designated as enzyme-treated lipid B. Enzyme-treated lipid B
Contained 97% by weight of solids and 83% by weight of lysophospholipids.

【0025】・酵素処理脂質Bの調製法に於て、酵素の
反応時間を8hrとしたほかは同じ方法で得たものを酵
素処理脂質Cとした。酵素処理脂質Cは固形分96重量
%、リゾリン脂質を67重量%含んだ。
In the method for preparing the enzyme-treated lipid B, the enzyme-treated lipid C was obtained by the same method except that the reaction time of the enzyme was 8 hr. The enzyme-treated lipid C contained 96% by weight of solid content and 67% by weight of lysophospholipid.

【0026】<脂肪酸> ・日本油脂(株)製、ヤシ油脂肪酸 ・日本油脂(株)製、大豆油脂肪酸<Fatty acid> -NOF CORPORATION, coconut oil fatty acid-NOF Co., soybean oil fatty acid

【0027】実施例1 ホートク物産のハイモクサン1重量部に、酵素処理脂質
Bの10重量%水溶液1重量部を加え、組成物水溶液2
重量部を得た(この組成物水溶液には、木酢液50重量
%、リゾリン脂質純分4.2重量%を含む)。
Example 1 1 part by weight of a 10% by weight aqueous solution of the enzyme-treated lipid B was added to 1 part by weight of high-moxan from Hortoku Co., Ltd.
By weight, 50% by weight of wood vinegar and 4.2% by weight of pure lysophospholipids were contained in this composition aqueous solution.

【0028】実施例2 信濃有機製中和木酢液8重量部に、酵素処理脂質B2重
量部、水道水10重量部を加えて加熱溶解し、組成物水
溶液20重量部を得た。
Example 2 2 parts by weight of enzyme-treated lipid B and 10 parts by weight of tap water were added to 8 parts by weight of a Shinano Organic neutralized wood vinegar solution and dissolved by heating to obtain 20 parts by weight of a composition aqueous solution.

【0029】実施例3 ホートク物産のハイモクサン5部に、酵素処理脂質Cの
10重量部、水溶液15部を加え混合溶液を20部とし
た。
Example 3 10 parts by weight of enzyme-treated lipid C and 15 parts by weight of an aqueous solution were added to 5 parts by weight of high-moxan from Hortoku Co., Ltd. to make a mixed solution of 20 parts.

【0030】実施例4 信濃有機製中和木酢液5重量部に、酵素処理脂質A5重
量部、水道水40重量部を加えて加熱溶解し混合液を5
0重量部とした。
Example 4 To 5 parts by weight of neutralized wood vinegar made by Shinano Organic Co., 5 parts by weight of enzyme-treated lipid A and 40 parts by weight of tap water were added and dissolved by heating to give a mixed solution of 5 parts.
It was 0 part by weight.

【0031】実施例5 重量部で、ホートク物産のハイモクサン90部、酵素処
理脂質B6部、ヤシ油脂肪酸4部を加熱溶解し、組成物
100部を得た。
Example 5 By weight, 90 parts of high moxan from Hotoku Co., 6 parts of enzyme-treated lipid B and 4 parts of coconut oil fatty acid were dissolved by heating to obtain 100 parts of a composition.

【0032】実施例6 重量でハイモクサン木酢液94部、酵素処理脂質C4
部、大豆油脂肪酸2部を加熱混合して、組成物を得た。
Example 6 94 parts by weight of high-moxan wood vinegar, enzyme-treated lipid C4
And 2 parts of soybean oil fatty acid were mixed by heating to obtain a composition.

【0033】実施例7 重量部で、ハイモクサン木酢液9、酵素処理脂質A1、
水道水10の比で加熱混合して20部の組成物を得た。
Example 7 In parts by weight, high-moxan wood vinegar solution 9, enzyme-treated lipid A1,
20 parts of the composition was obtained by heating and mixing with a ratio of 10 tap water.

【0034】実施例8 重量部で、信濃有機の中和木酢液6、酵素処理脂質B
4、水道水10を加熱混合して20部の組成物を得た。
Example 8 6 parts by weight of Shinano Organic Neutralized Wood Vinegar Solution 6 and Enzyme Treated Lipid B
4, tap water 10 was heated and mixed to obtain 20 parts of the composition.

【0035】実施例9 重量部で、ハイモクサン木酢液80、酵素処理脂質C1
5、ヤシ油脂肪酸5、水道水100を加熱溶解して20
0部の組成物を得た。
Example 9 By weight, high-moxan wood vinegar solution 80 and enzyme-treated lipid C1
5, coconut oil fatty acid 5, tap water 100 dissolved by heating 20
0 part of composition was obtained.

【0036】実施例10 重量部で、ハイモクサン木酢液81、酵素処理脂質A1
5、大豆油脂肪酸4、水道水200を加熱溶解して30
0部の組成物を得た。
Example 10 By weight, high-moxan wood vinegar solution 81 and enzyme-treated lipid A1
5, soybean oil fatty acid 4, tap water 200 dissolved by heating 30
0 part of composition was obtained.

【0037】[0037]

【実験例】実験例1 苗から5年間育成後のツバキ畑、1a(5m×10m)
を4等分した試験区について、6月上旬と8月上旬の2
回の散布試験を行った。対照区1としてハイモクサン木
酢液の200倍希釈液を、対照区2として酵素処理脂質
Bの0.05%水溶液を、2カ所の試験区には、実施例
1、実施例7の組成物の水溶液を木酢液換算で200倍
に希釈したものを、それぞれ、350ml/m2 散布し
た、9月上旬に於て、両対照区にはアブラムシ、カイガ
ラムシの付着がみられたが、本発明の組成物の試験区で
はそれらを見いだすことは困難だった。また翌年2月時
点で、両対照区ではツバキモチ病やスス病が認められた
が、試験区では異常がなく、樹勢が良好であった。
[Experimental example] Experimental example 1 Camellia field after growing for 5 years from seedling, 1a (5m x 10m)
About the test area divided into four, 2 in early June and early August
One spray test was performed. As a control group 1, a 200-fold diluted solution of high-moxan wood vinegar solution, as a control group 2, a 0.05% aqueous solution of enzyme-treated lipid B, and in two test groups, an aqueous solution of the composition of Example 1 and Example 7. Each of the control plots was sprayed with 350 ml / m 2 of a 200-fold diluted solution of wood vinegar, and aphids and scale insects were found to adhere to both control groups in early September. It was difficult to find them in our test plot. As of February of the following year, camellia vulgaris disease and soot disease were observed in both control plots, but there was no abnormality in the test plots and the vigor was good.

【0038】実験例2 約5m2 の密生したオオムラサキツツジの植え込み4カ
所について、5月上旬の刈り込み後、7月、9月の各月
の上旬に3回の散布試験を行った。対照区としてハイモ
クサン木酢液の200倍液、3カ所の試験区には、実施
例5、実施例6、実施例9の組成物を木酢液換算で20
0倍の希釈液として、それぞれ、400ml/m2 散布
した。対照区では葉面へのハダニ付着、グンパイ虫の食
害による中程度の葉の白色化、ルリチュウレンジによる
葉の食害が起こったが、3つの試験区では害虫被害が認
められなかった。また試験区では対照区に比べて、葉の
色付きがよく、花芽の着生が1.5倍程度になった。
Experimental Example 2 About 4 places of densely planted Oomurasaki azalea of about 5 m 2 were sprayed three times at the beginning of each month of July and September after pruning at the beginning of May. As a control group, a 200-fold solution of high-moxan wood vinegar solution, and in three test groups, the compositions of Example 5, Example 6 and Example 9 were converted to 20 times in terms of wood vinegar solution.
As a 0-fold diluted solution, 400 ml / m 2 was sprayed on each. In the control plots, mite adhesion on the leaf surface, moderate leaf whitening due to feeding damage of Gunpai insects, and leaf feeding damage due to Rurichurange were caused, but no pest damage was observed in the three test plots. In the test plot, the leaves were better colored and the flower buds were about 1.5 times as much as the control plot.

【0039】実験例3 盛り土のり面保護のため、4月に播種し5月に発芽した
ケンタッキイグラスに対し、同一条件の斜面を5カ所に
区切り、6月下旬に散布試験を行った。対照区1には信
濃有機の中和木酢液を400倍に希釈したものを、対照
区2には同じく信濃有機の木酢液の散布の1日後に、酵
素処理脂質Aの0.25%水溶液を散布し、2カ所の試
験区には、それぞれ、実施例4及び実施例8の組成物の
木酢液換算で400倍に調整した水溶液を散布した。散
布量は1m2 あたり200mlとした。8月下旬に於け
る各区の生育状況は両試験区が最も良好で、緑色が強
く、一見して区別できた。次いで対照区2が良好で、対
照区1がそれに劣ったが、無試験区よりはよかった。
Experimental Example 3 For protection of the embankment slope, Kentacchii grass seeded in April and germinated in May was divided into 5 slopes under the same conditions, and a spraying test was conducted in late June. The control group 1 was prepared by diluting the Shinano organic neutralized wood vinegar solution 400 times, and the control group 2 was also treated with the 0.25% aqueous solution of the enzyme-treated lipid A one day after spraying the Shinano organic wood vinegar solution. An aqueous solution adjusted to 400 times in terms of the wood vinegar solution of the compositions of Example 4 and Example 8 was applied to each of the two test plots. The amount of spray was 200 ml per 1 m 2 . The growth status of each plot in the latter part of August was the best in both test plots, and the green color was strong, and it was possible to distinguish at a glance. Next, the control group 2 was good and the control group 1 was inferior thereto, but it was better than the non-test group.

【0040】実験例4 千宝菜の無農薬栽培において、対照区は信濃有機の中和
木酢液の500倍液を、試験区は実施例2の組成物水溶
液を木酢液換算で500倍としたものを用いた。地上部
の体長が約5cmに達した時から、15日間隔で25l
/aの量を3回葉面散布を行ったところ、無試験区に対
して、対照区は7日、試験区は12日早く収穫できた。
Experimental Example 4 In pesticide-free cultivation of Senbokusai, the control group was 500 times the neutralized wood vinegar solution of Shinano Organic, and the test group was 500 times the aqueous solution of the composition of Example 2 in terms of wood vinegar solution. I used one. 25l at 15-day intervals from when the length of the above-ground part reached about 5cm
When the amount of / a was sprayed on the leaves three times, the control plot was able to be harvested 7 days earlier and the test plot was harvested 12 days earlier than the non-test plot.

【0041】実験例5 アスパラガスの栽培において、5月上旬から1カ月おき
に、土壌・葉面散布として5回の散布を行った。散布量
は35l/aで、対照区にはハイモクサン木酢液の50
0倍液を、試験区1には実施例3、試験区2には実施例
10の組成物の木酢液換算500倍水溶液を散布した。
春取り収穫日数は無試験区の52日に対して、対照区:
58日、試験区1:63日、試験区2:65日であり、
収穫量は無試験区に対して、対照区:1.10倍、試験
区1と2はそれぞれ、1.18倍、1.21倍になっ
た。また秋取りの収量倍率はは、それぞれ順番に、1.
08、1.13、1.15であった。
Experimental Example 5 In the cultivation of asparagus, application was performed 5 times as soil / foliage application every other month from the beginning of May. The amount of spray is 35l / a, and 50m of high-moxan wood vinegar is used in the control area.
The test solution 1 was sprayed with a 0-fold solution, and the test solution 2 was sprayed with a 500-fold aqueous solution of the composition of Example 10 converted into a wooden vinegar solution.
The spring harvest time is 52 days in the non-test area, whereas the control area is:
58 days, test area 1:63 days, test area 2:65 days,
The amount of harvest was 1.10 times as much as that in the non-test section, and 1.18 times and 1.21 times as much in test sections 1 and 2, respectively. In addition, the yield ratios for autumn are 1.
It was 08, 1.13 and 1.15.

【0042】実験例6 サラサドウダンツツジの挿し木に於て、6月下旬に採取
した挿し穂を、実施例1の組成物水溶液の100倍希釈
液に10時間浸した後、100本を鹿沼土に挿し木し
た。挿し木後は15日間隔で2回、同組成物水溶液の2
00倍液3リットルを灌水した。対照として、水道水の
みを用いた無処理区を全く同様にしてもうけて比較し
た。10月下旬の段階で活着率は、試験区で91%、対
照は63%であり、試験区苗の1本当りの発根重量は対
照区の1.6倍だった。
Experimental Example 6 For cuttings of Amaranthaceae, cuttings collected in late June were soaked in a 100-fold dilution of the composition aqueous solution of Example 1 for 10 hours, and 100 cuttings were cut into Kanuma soil. did. After cutting, 2 times with an aqueous solution of the same composition twice every 15 days.
3 liters of a 00-fold solution was irrigated. As a control, an untreated plot using only tap water was prepared in the same manner and compared. At the stage of late October, the survival rate was 91% in the test plot and 63% in the control plot, and the rooting weight per seedling in the test plot was 1.6 times that in the control plot.

【0043】[0043]

【発明の効果】本発明の効果は、実験例1ー6に示した
通りである。即ち、第1の発明の木酢液/リゾリン脂質
からなる組成物、第2の発明の木酢液/リゾリン脂質/
脂肪酸からなる組成物の双方ともに、本発明の目的であ
る、効力の大きい天然系の農薬に類似する組成物を得る
ことに成功し、従来の木酢液の作用が飛躍的に改良され
たことにある。また植物の栄養状態の改良に於て、単な
る木酢液よりもはるかに大きな効果の得られたことにあ
る。
The effects of the present invention are as shown in Experimental Examples 1-6. That is, a composition comprising the wood vinegar of the first invention / lysophospholipid, the wood vinegar of the second invention / lysophospholipid /
Both of the compositions consisting of fatty acids, which is the object of the present invention, succeeded in obtaining a composition similar to a highly effective natural pesticide, and the action of conventional wood vinegar was dramatically improved. is there. Moreover, in improving the nutritional condition of plants, it is possible to obtain a far greater effect than simple wood vinegar.

Claims (9)

【特許請求の範囲】[Claims] 【請求項1】 木酢液とリゾリン脂質とを含む植物活性
農薬組成物。
1. A plant activity containing wood vinegar and lysophospholipid
Chemical pesticide composition.
【請求項2】 木酢液/リゾリン脂質の重量比が20:
80−97:3である請求項1記載の農薬組成物。
2. The weight ratio of wood vinegar / lysophospholipid is 20:
The pesticidal composition according to claim 1, which is 80-97: 3.
【請求項3】 リゾリン脂質が大豆リゾリン脂質であ
る、請求項1または2記載の農薬組成物。
3. A lysophospholipid is a soybean lysophospholipid, according to claim 1 or 2 agrochemical composition.
【請求項4】 木酢液とリゾリン脂質及び脂肪酸とを含
植物活性化農薬組成物。
4. A plant activated pesticide composition comprising wood vinegar, lysophospholipids and fatty acids.
【請求項5】 木酢液/リゾリン脂質の重量比が20:
80−97:3であり、さらにリゾリン脂質に対して1
00重量%以下の脂肪酸を含む請求項4記載の農薬組成
物。
5. A wood vinegar solution / lysophospholipids weight ratio of 20:
80-97: 3, and 1 for lysophospholipid
The pesticide composition according to claim 4, which contains not more than 00% by weight of a fatty acid.
【請求項6】 リゾリン脂質が大豆リゾリン脂質である
請求項4または5記載の農薬組成物。
6. The method of claim 4 or 5 agrochemical composition according lysophospholipids are soybean lysophospholipid.
【請求項7】 脂肪酸が不飽和脂肪酸である請求項4
たは5記載の農薬組成物。
Claim 7. The fatty acid is an unsaturated fatty acid 4 or
Pesticidal compositions of other 5 wherein.
【請求項8】 脂肪酸が不飽和脂肪酸及び炭素原子数8
−14の中鎖脂肪酸である請求項4または5記載の農薬
組成物。
8. The unsaturated fatty acid and the fatty acid having 8 carbon atoms
The pesticide composition according to claim 4 or 5, which is a medium chain fatty acid of -14.
【請求項9】 脂肪酸が炭素原子数8−14の中鎖脂肪
酸である請求項4または5記載の農薬組成物。
9. fatty claim 4 or 5 agrochemical composition wherein the medium chain fatty acid having a carbon number of 8-14.
JP2295092A 1992-02-07 1992-02-07 Agrochemical composition consisting of natural products Expired - Lifetime JPH0751489B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2295092A JPH0751489B2 (en) 1992-02-07 1992-02-07 Agrochemical composition consisting of natural products

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Publication Number Publication Date
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JPH0751489B2 true JPH0751489B2 (en) 1995-06-05

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ID=12096898

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JP (1) JPH0751489B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000160476A (en) * 1998-11-30 2000-06-13 E Tec:Kk Production of carbon fiber and carbon fiber produced thereby
JP3805599B2 (en) * 2000-04-10 2006-08-02 花王株式会社 Plant vitality agent
JP2001316204A (en) * 2000-04-28 2001-11-13 Kao Corp Agent for vitalizing plant
JP5809449B2 (en) * 2011-05-27 2015-11-10 住友化学園芸株式会社 Agricultural and horticultural insecticidal compositions
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