JPS606319B2 - A plant breeding agent that improves the physical, chemical, and biological aspects of soil and imparts soil fertility. - Google Patents

A plant breeding agent that improves the physical, chemical, and biological aspects of soil and imparts soil fertility.

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Publication number
JPS606319B2
JPS606319B2 JP53139240A JP13924078A JPS606319B2 JP S606319 B2 JPS606319 B2 JP S606319B2 JP 53139240 A JP53139240 A JP 53139240A JP 13924078 A JP13924078 A JP 13924078A JP S606319 B2 JPS606319 B2 JP S606319B2
Authority
JP
Japan
Prior art keywords
lfn
silicon
chloride
soil
hydrogen
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
JP53139240A
Other languages
Japanese (ja)
Other versions
JPS5565290A (en
Inventor
健吉 立木
義輝 佐田
豊 山下
怜 遠藤
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.)
JIN RIKAGAKU KENKYUSHO KK
Original Assignee
JIN RIKAGAKU KENKYUSHO KK
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 JIN RIKAGAKU KENKYUSHO KK filed Critical JIN RIKAGAKU KENKYUSHO KK
Priority to JP53139240A priority Critical patent/JPS606319B2/en
Publication of JPS5565290A publication Critical patent/JPS5565290A/en
Publication of JPS606319B2 publication Critical patent/JPS606319B2/en
Expired legal-status Critical Current

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  • Fertilizers (AREA)

Description

【発明の詳細な説明】 本発明は、新規な土壌改良兼植物育成剤に関するが、更
に詳しくは、窒素化した珪水塩化物を生魚体とともに発
酵させたものを含有せしめてなる全く新規な土壌改良兼
植物育成剤に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel soil improvement and plant growth agent, and more specifically, to a completely novel soil containing nitrogenated silica chloride fermented with raw fish bodies. This relates to an improvement and plant breeding agent.

本発明者は、珪素塩化物の各種誘導体について研究を行
ったところ、珪水塩化物(HSi3CI7)をヒドラジ
ンで処理して得た窒素化珪水塩化物(CI6Si3(N
H2)・H)が極めて特異的な生理活性を有するという
新規な知見を得、この新知見に基づき鋭意研究を行った
結果、この窒素化珪水塩化物を生魚体とともに発酵させ
たものは高い植物浸透性を示し、土壌に施用した場合土
壌の物理、化学、生物的様相を改善することは勿論のこ
と、葵面施用した場合も、著しい植物成長促進作用、結
実増加作用、連作障害防止作用といった特殊な植物育成
作用を有することをつきとめ、本発明を完成したのであ
る。
The present inventor conducted research on various derivatives of silicon chloride, and found that nitrogenated silica chloride (CI6Si3 (N
We obtained new knowledge that H2) and H) have extremely specific physiological activities, and as a result of intensive research based on this new knowledge, we found that this nitrogenated silica chloride fermented with raw fish bodies has a high It exhibits permeability to plants, and when applied to the soil, it not only improves the physical, chemical, and biological aspects of the soil, but also has a remarkable effect of promoting plant growth, increasing fruit set, and preventing damage to continuous cropping when applied to the hollyhock side. They discovered that it has a special plant-growing effect, and completed the present invention.

即ち、本発明は、次に述べるところの窒素化した珪水塩
化物を有効成分として含有せしめたことを特徴とする土
壌改良兼植物育成剤である。
That is, the present invention is a soil improvement and plant growth agent characterized by containing the following nitrogenated silica chloride as an active ingredient.

本発明に係る窒素化した窪水塩化物と生魚体との発酵製
品は、次のようにして製造する。まずはじめに、予め空
気に接触させた珪素の塩化物(即ち、四塩化珪素、六辻
副ヒ珪素、又は八塩化珪素)に、塩化水素ガスを夫々の
2%以上共存させておき、これを200℃以上の温度で
水素と反応させて、珪素塩化物を製造する。
The fermented product of nitrogenated pit water chloride and raw fish according to the present invention is produced as follows. First, silicon chloride (i.e., silicon tetrachloride, silicon arsenic, or silicon octachloride) which has been brought into contact with air in advance is made to coexist with hydrogen chloride gas in an amount of 2% or more. Silicon chloride is produced by reacting with hydrogen at temperatures above ℃.

原料として使用する珪素の塩化物は、その純度が充分に
高いものでなければならず、そのために通常は、市販さ
れている塩化珪素を数回蒸留して使用する。
The silicon chloride used as a raw material must have a sufficiently high purity, and for this purpose, commercially available silicon chloride is usually distilled several times before use.

このようにして精製した塩化珪素は、充分に空気と接触
させておき、次いで塩化水素ガスを共存させる。
The silicon chloride purified in this manner is brought into sufficient contact with air, and then hydrogen chloride gas is allowed to coexist.

共存させる塩化水素ガスの量は、2%以上である。これ
よりも少ないと反応の進行が遅れる。塩化水素ガスの量
が多い程反応は容易になる。塩化水素ガスを共存せしめ
る手段としては、例えば、予じめ低温のもとで塩化水素
ガスを珪素の塩化物に溶解しておき、これを反応室に導
いて気化使用してもよいし、また、気化した珪素の塩化
物に塩化水素ガスを混合して使用してもよいが、前者の
方法が好適である。次に、塩化珪素は、塩化水素ガス共
存下において、水素と反応せしめて珪水塩化物とするの
であるが、この塩化珪素と水素との反応は、双方を接触
させて反応させるのであればどのような方法も採用する
ことができる。
The amount of hydrogen chloride gas coexisting is 2% or more. If the amount is less than this, the progress of the reaction will be delayed. The larger the amount of hydrogen chloride gas, the easier the reaction will be. As a means of making hydrogen chloride gas coexist, for example, hydrogen chloride gas may be dissolved in silicon chloride at a low temperature in advance, and this may be introduced into a reaction chamber and used for vaporization. Although hydrogen chloride gas may be mixed with vaporized silicon chloride, the former method is preferred. Next, silicon chloride is reacted with hydrogen in the coexistence of hydrogen chloride gas to form silica chloride. Such a method can also be adopted.

通常は、気相で反応させるのが好適であって、例えば、
ノズルを用いて塩化珪素及び水素双方のガスを接触させ
る方法によれば反応を円滑に行わせることができる。双
方のガスの反応比率は、原料の種類、反応条件その他に
よって広範囲に変えることができるが、好適なガスの量
比は、塩化珪素1モルに対し水素0.5〜10モル、特
に好適には水素1.5〜5モルであって、この範囲内で
反応を行うと特に品質のすぐれた珪水塩化物が得られる
。反応温度は、200〜700℃である。200qo未
満では反応が充分に進行しないので、20000以上の
温度で反応させることが必須の要件である。
Usually, it is preferable to carry out the reaction in the gas phase, for example,
By using a nozzle to bring both silicon chloride and hydrogen gases into contact with each other, the reaction can be carried out smoothly. The reaction ratio of both gases can be varied widely depending on the type of raw materials, reaction conditions, etc., but the preferred gas ratio is 0.5 to 10 moles of hydrogen per mole of silicon chloride, particularly preferably 0.5 to 10 moles of hydrogen. When the amount of hydrogen is 1.5 to 5 moles and the reaction is carried out within this range, a silica chloride of particularly excellent quality can be obtained. The reaction temperature is 200-700°C. If the temperature is less than 200 qo, the reaction will not proceed sufficiently, so it is essential to carry out the reaction at a temperature of 20,000 qo or higher.

反応温度は高い方が効率的であるが、熱経済性を考慮す
ると700qo以上とするのは好ましいことではない。
原料として使用する塩化珪素は、上記したように充分精
製したものでなければならないが、これに共存させる塩
化水素は、極端にその純度をあげる必要はないけれども
、水分は充分に除去しておくのが良い。
Although the higher the reaction temperature, the more efficient it is, it is not preferable to set the reaction temperature to 700 qo or more in consideration of thermoeconomic efficiency.
The silicon chloride used as a raw material must be sufficiently purified as described above, but the hydrogen chloride coexisting with it does not need to be extremely purified, but it is important to remove moisture sufficiently. is good.

反応に用いる水素は、通常の方法で製造された市販品を
用いても何ら差仕えはない。原料として使用する塩化珪
素としては、四塩化珪素のみならず、六塩化珪素、八塩
化珪素も全く同機に使用することが可能である。六塩化
珪素、八塩化珪素は、四塩化珪素に比して反応が容易で
あるので、反応温度も比較的低温で充分であるし、共存
させる塩化水素の量も四塩化珪素の場合よりも少量で充
分である。このような反応によって得られた珪水塩化物
(以下、これを「LFN−11という。
There is no difference in hydrogen used in the reaction even if a commercially available product produced by a conventional method is used. As the silicon chloride used as a raw material, not only silicon tetrachloride but also silicon hexachloride and silicon octachloride can be used in the same machine. Silicon hexachloride and silicon octachloride react more easily than silicon tetrachloride, so a relatively low reaction temperature is sufficient, and the amount of hydrogen chloride coexisting is smaller than that of silicon tetrachloride. is sufficient. Silica chloride obtained by such a reaction (hereinafter referred to as "LFN-11").

)は、無色で刺激性が強い液体であって、比重が1.4
前後、1%溶液の解が0.7〜0.9という強酸性の物
性を有する。このようにして得られた珪水塩化物(LF
N−1)を一旦ガス化し、そのガスを水に吸収溶解させ
るが、その重量比率は、水100に対して液相として2
〜5、特に2.5〜3.M寸近が適当である。
) is a colorless, highly irritating liquid with a specific gravity of 1.4.
It has strong acidic physical properties with a solution of 0.7 to 0.9 in a 1% solution. Silica chloride (LF
N-1) is once gasified and the gas is absorbed and dissolved in water, but the weight ratio is 2 as a liquid phase to 100 parts of water.
~5, especially 2.5~3. A value close to M is appropriate.

これを、常温で、ヒドラジンと反応させる。反応方式は
、水に吸収溶解せしめたLFN−1とヒドラジンとを接
触させるものであればすべての方式が適宜使用される。
通常は、上記によって得られたLFN−1水溶液にN2
比を常温で溶解反応させる。反応比率は、N2比80%
として、0.1〜5%、好ましくは0.4〜0.8%で
ある。次いでアルカリを加えて中和する。アルカリ化剤
としては、ナトリウム、カリウム、カルシウム、マグネ
シウム等の酸化物「水酸化物といった通常のアルカリが
適宜使用できるが、Ca(OH)2等は特に好適なアル
カリ化剤の例である。このようにして、窒素化したLF
N−1が得られるが(以下、これを「LFN一2」とい
う。)、上記中和反応工程中において、Si02が析出
することがあり、これは櫨過することによって除去する
。このようにして得られたLFN−2は、斑7.0比重
1.0の無色透明液体である。このLFN‐2を原料と
して本発明の有効成分化合物である発酵製品を製造する
のであるが、それには先ず、上記のようにして製造した
LFN−2を水で稀釈する。
This is reacted with hydrazine at room temperature. Any reaction method may be used as appropriate, as long as it brings LFN-1 absorbed and dissolved in water into contact with hydrazine.
Usually, N2 is added to the LFN-1 aqueous solution obtained above.
The ratio is dissolved and reacted at room temperature. Reaction ratio is 80% N2 ratio
It is 0.1 to 5%, preferably 0.4 to 0.8%. Then add an alkali to neutralize. As the alkalizing agent, ordinary alkalis such as oxides and hydroxides of sodium, potassium, calcium, magnesium, etc. can be used as appropriate, but Ca(OH)2 and the like are particularly suitable examples of the alkalizing agent. In this way, nitrogenized LF
Although N-1 is obtained (hereinafter referred to as "LFN-2"), Si02 may be precipitated during the above neutralization reaction step, and this is removed by filtration. LFN-2 thus obtained is a colorless transparent liquid with a speck of 7.0 and a specific gravity of 1.0. A fermented product, which is the active ingredient compound of the present invention, is produced using this LFN-2 as a raw material. First, the LFN-2 produced as described above is diluted with water.

稀釈割合は、含有塩素量が0.01〜10%、好適には
1〜8%程度となるようにするのがよい。次に、稀釈し
たLFN一2液に生魚体を加え、発酵させて発酵製品を
得る。
The dilution ratio is preferably such that the amount of chlorine contained is about 0.01 to 10%, preferably about 1 to 8%. Next, raw fish bodies are added to the diluted LFN solution and fermented to obtain a fermented product.

稀釈LFN一2液と生魚体との混合比は、1:0.5〜
1:10、好適には1:1〜1:5である。生魚体は「
粉砕することなくそのまま使用してもよいが、発酵促進
のために細かく粉砕した方が良い。生魚体としては、全
魚体をそのまま用いてもよいし、内臓のみでもよく、ま
た魚肉を用いても勿論差仕えない。発酵は「自然発酵に
まかせておいて充分であり、別に種菌を接種することは
ないし、発酵温度は室温で充分であるが、冬期には少し
加溢してやると良い。発酵所要期間は、常温で5〜15
日程度であるが、通常、1週間は必要である。このよう
にして得られた発酵製品は、そのま)用いてもよいが必
要ある場合には、猿過、遠心分離その他の常法によって
固液分離を行った後、通常は、製剤化を行って粉剤又は
液剤として実際に使用する。
The mixing ratio of diluted LFN liquid and raw fish is 1:0.5~
The ratio is 1:10, preferably 1:1 to 1:5. The raw fish body is
You can use it as is without pulverizing it, but it is better to pulverize it finely to promote fermentation. As for the raw fish, the whole fish may be used as is, only the internal organs may be used, and of course there is no difference in the use of fish meat. For fermentation, it is sufficient to leave it to natural fermentation, there is no need to inoculate the starter, and the fermentation temperature is sufficient at room temperature, but in winter it is a good idea to add a little overflow. 5-15
Usually, it takes about a week. The fermented product thus obtained may be used as is, but if necessary, it is usually formulated into a formulation after solid-liquid separation by sieving, centrifugation or other conventional methods. It is actually used as a powder or liquid.

本発明の有効成分化合物である発酵製品(これを、以下
「LFN−3」という。
Fermented product which is the active ingredient compound of the present invention (hereinafter referred to as "LFN-3").

)の製造実施例を、参考例として以下に示す。参考例
1 5回蒸留した四塩化珪素lkgを予め空気に接触させて
おき、貯槽ビンに入れ、これを冷却して塩化水素ガスを
80タ落籍させる。
) is shown below as a reference example. Reference example
1. 1 kg of silicon tetrachloride distilled 5 times is brought into contact with air in advance, placed in a storage bottle, and cooled to release 80 tons of hydrogen chloride gas.

他方、水素を内圧lk9のタンクに貯える。これらを、
400つ0に加熱してある四塩化珪素気化装置並びに水
素加熱装置に夫々バルブを開いてポンプ及び目圧で送入
する。400qoに加熱したノズルを通して、加熱気化
した四塩化珪素ガスと水素ガスを送入し、反応器内で4
00qoで接触反応させる。
On the other hand, hydrogen is stored in a tank with an internal pressure of lk9. these,
The valves were opened to the silicon tetrachloride vaporizer and hydrogen heating device, which were heated to 400°C, and the mixture was fed into the silicon tetrachloride vaporizer and the hydrogen heating device using a pump and eye pressure. Heat-vaporized silicon tetrachloride gas and hydrogen gas are fed through a nozzle heated to 400 qo, and 400 qo is heated in the reactor.
Contact reaction is carried out at 00qo.

双方のガスの流量比は、四塩化珪素1モルに対して水素
2モルの比率に保持する。接触反応終了後のガスは、こ
れを冷却した捕集に導き凝縮させる。こ)で未反応のガ
スは分離する。このようにして、珪水塩化物(LFN−
1)が、無色で刺激性が強く、比重が1.40〜1.4
を1%溶液のpHが0.8の液体として、収率90%で
得られる。このようにして得られたLFN−1を、常温
で一日ガス化し、水100に対して液相として3.0の
重量比率で、水に吸収溶解させる。
The flow rate ratio of both gases is maintained at a ratio of 2 moles of hydrogen to 1 mole of silicon tetrachloride. The gas after the completion of the contact reaction is guided to a cooled collection and condensed. This) separates unreacted gas. In this way, silica chloride (LFN-
1) is colorless, highly irritating, and has a specific gravity of 1.40 to 1.4.
is obtained as a 1% solution of a liquid with a pH of 0.8 in a yield of 90%. The LFN-1 thus obtained is gasified at room temperature for one day, and absorbed and dissolved in water at a weight ratio of 3.0 as a liquid phase to 100 parts of water.

これにヒドラジンを常温で溶解反応させるが、その反応
比率は、N2比80%として、0.5%とする。反応液
にCa(OH)2を添加して、そのpHが7.0になる
まで中和反応させる。析出するSi02を櫨過して除去
する。このようにして、窒素化した珪水塩化物(LFN
−2)が、pH7,0、比重1.0の無色透明の液体と
して得られる。LFN−2を水で稀釈してその含有CI
量を4%とした後、生の鰯荒を粉砕し、タンクで混合し
て、20qoで発酵させる。
Hydrazine is dissolved and reacted with this at room temperature, and the reaction ratio is 0.5% with the N2 ratio being 80%. Ca(OH)2 is added to the reaction solution, and a neutralization reaction is carried out until the pH becomes 7.0. The precipitated Si02 is removed by filtration. In this way, nitrogenated silica chloride (LFN
-2) is obtained as a colorless and transparent liquid with a pH of 7.0 and a specific gravity of 1.0. LFN-2 was diluted with water and its containing CI
After adjusting the amount to 4%, raw sardine grains are crushed, mixed in a tank, and fermented at 20 qo.

稀釈LFN−2と鰯荒との混合比は、1:1.2とし、
7日間発酵させた。このようにして本発明に係る有効成
分である発酵製品(LFN−3)が得られた。参考例
2 ,5回蒸留した六塩化珪素lk9に対し塩化水素ガス4
0夕を溶解させた後、参考例1と同様に処理してLFN
−3を同様の収率で得た。
The mixing ratio of diluted LFN-2 and sardine roughness was 1:1.2,
Fermented for 7 days. In this way, a fermented product (LFN-3), which is an active ingredient according to the present invention, was obtained. Reference example
2. Hydrogen chloride gas 4 to 5 times distilled silicon hexachloride lk 9
After dissolving LFN, it was treated in the same manner as in Reference Example 1.
-3 was obtained in similar yield.

但し、六塩化珪素1モルに対する水素の反応比率は、3
.5モルとし、反応温度は30び○とし、生魚としては
、鰯を内臓、頭、尾、骨等の分離を行うことなく全体を
使用した。参考例 3 5回蒸留した八塩化珪素を用い、参考例1の方法をくり
返してLFN−2を得た。
However, the reaction ratio of hydrogen to 1 mole of silicon hexachloride is 3
.. 5 mol, the reaction temperature was 30°C, and the whole sardine was used as raw fish without separating the internal organs, head, tail, bones, etc. Reference Example 3 LFN-2 was obtained by repeating the method of Reference Example 1 using silicon octachloride that had been distilled five times.

但し、八塩化珪素と水素の反応比率は、1:4モルとし
、反応温度は250℃、ヒドラジン(80%)の反応比
率は、0.4%とし、生魚荒と稀釈LFN−2との混合
比は1:1.4とし、発酵は25qoで7日間継続せし
めた。このようにして製造したLFN−3は、生理活性
が強く、植物に対する浸透性も顕著で、これを植物に対
して適用したところ卓越した生長促進、結実増加、品質
上昇、連作障害の防止といったすぐれた土壌改良及び植
物育成作用を有することをつきとめた。
However, the reaction ratio of silicon octachloride and hydrogen was 1:4 mol, the reaction temperature was 250°C, the reaction ratio of hydrazine (80%) was 0.4%, and the mixture of raw raw fish and diluted LFN-2 was The ratio was 1:1.4 and fermentation was continued for 7 days at 25 qo. LFN-3 produced in this way has strong physiological activity and remarkable permeability to plants, and when applied to plants, it has excellent growth promotion, increased fruit set, improved quality, and prevention of continuous cropping failure. It has been found that it has soil improvement and plant growth effects.

そして更に研究をすすめた結果、LFN−3は、植物に
対する薬害もなく、耐膜性があり、その他農業用担体、
補助剤との協調性も良好であるうえ、葉面散布、土壌中
への溝注、いづれの方法でも適用できるという新知見を
得て、LFN−3が土壌改良兼植物育成剤として実施に
供することができることを確認し、また粉末化した貝化
石にLFN一3を混練して、これを土壌に散布すると、
堆肥を使用したと同じ状態となり、±磯の物理、イb学
、生物的様相が一変して植物の生育、品質の向上及び病
虫害の防除効果が、LFN−3の単独使用よりも更に向
上することを確認し、本発明を完成したものである。本
発明に係る有効成分は、使用目的によって直接適用する
か、または適当な液状担体に溶解するか、あるいはこれ
に分散させ、または適当な固体担体と混合するか、ある
いはこれに吸着させ、更に必要ある場合には、これらに
、分散剤、乳化剤、懸濁剤、展着剤、浸透剤、湿潤剤、
安定剤等を添加し、水和剤、乳剤、油剤、粉剤、錠剤、
粒剤止噴霧剤等の剤型として使用する。
Further research revealed that LFN-3 has no phytotoxicity to plants, is membrane resistant, and can be used as a carrier for other agricultural purposes.
New knowledge has been obtained that LFN-3 works well with adjuvants and can be applied either by foliar spraying or by pouring into the soil, allowing LFN-3 to be used as a soil improvement and plant growth agent. We also confirmed that it was possible to do this by mixing LFN-3 with powdered shellfish fossils and spraying it on the soil.
The condition is the same as when compost is used, and the physical, biological, and biological aspects of the rock are completely changed, and the plant growth, quality improvement, and pest control effect are even better than when using LFN-3 alone. This was confirmed and the present invention was completed. The active ingredient according to the present invention can be applied directly, dissolved or dispersed in a suitable liquid carrier, mixed with a suitable solid carrier, or adsorbed thereto, depending on the purpose of use. In some cases, these include dispersants, emulsifiers, suspending agents, spreading agents, penetrating agents, wetting agents,
Add stabilizers, etc. to produce wettable powders, emulsions, oils, powders, tablets,
Used as a dosage form such as granules and anti-spray agents.

これらの調合物に他の殺菌剤、殺虫剤、毅ダニ剤、植物
生長調整剤等の農業用薬剤を混用することも可能である
。また、肥料用担体と混合して粉状、液状、粒状肥料の
形態にして土壌に適用したり、葵面に直接適用したりし
てもよい。
It is also possible to mix these preparations with other agricultural chemicals such as fungicides, insecticides, acaricides, plant growth regulators, and the like. Further, it may be mixed with a fertilizer carrier and applied to the soil in the form of powder, liquid, or granular fertilizer, or it may be applied directly to the hollyhock surface.

この調合物に、窒素、リン酸、カリ等の無機合成肥料、
魚粕、油粕、堆肥、勤物糞尿等の有機質肥料を添加混合
することも可能である。次に本発明の実施例について記
述することにする。
This mixture contains inorganic synthetic fertilizers such as nitrogen, phosphoric acid, and potassium.
It is also possible to add and mix organic fertilizers such as fish meal, oil cake, compost, and manure. Next, embodiments of the present invention will be described.

実施例 1 昭和53王5月30日、水稲(金南風)種子を播種し、
6月30日に1′5000アールポットに3本ずつの苗
を移植した。
Example 1 On May 30th, 1976, paddy rice (Kinnanpu) seeds were sown.
Three seedlings were transplanted into 1'5,000 are pots on June 30th.

施肥量は、ポット当り硫安2夕、過燐酸石灰2夕、硫酸
カリ1夕とし、更にLFN−3の0.05%液1の‘を
基肥として施した。7月2日※日に抜取調査をしたが、
田植後10日毎に0.05%液の10鉢音稀釈液をまん
べんなく葵面に散布した。
The amount of fertilizer applied per pot was 2 nights of ammonium sulfate, 2 nights of lime superphosphate, and 1 night of potassium sulfate, and 1 part of 0.05% solution of LFN-3 was also applied as a base fertilizer. We conducted a sampling survey on July 2nd*.
Every 10 days after rice transplantation, 0.05% diluted solution was evenly sprayed on the hollyhock surface.

このようにして水稲に対する生育調査を行い、下記のよ
うな結果を得た。なお、LFN−3を全く使用しないポ
ケットを対照とした。実施例 2 静岡県奨励品種水稲である駿河もちを用い、1.也の水
田でLFN−3、肥料、農薬を次のように施用して生育
、収穫試験を行った。
In this way, we conducted a growth survey on paddy rice and obtained the following results. Note that a pocket in which no LFN-3 was used was used as a control. Example 2 Using Suruga Mochi, a rice variety recommended by Shizuoka Prefecture, 1. Growth and yield tests were conducted in Yano paddy fields by applying LFN-3, fertilizers, and pesticides as follows.

(注) 1.LFN−3 P′Lは、それぞれ実施例4
,5によって製造されたLFN−3の粉剤及び液剤であ
る。
(Note) 1. LFN-3 P'L is Example 4, respectively.
These are powder and liquid formulations of LFN-3 manufactured by Co., Ltd., 5.

2.(52.6.26)とは、LFN−3を施用した期
日、昭和52年6月26日を指す。
2. (52.6.26) refers to the date of application of LFN-3, June 26, 1978.

{a)LPN−3粉剤IP)の施用時期 本田に於て苗を植えつける1週背乃至10日前に(P)
を散布し土とよく混和させ姿すつ育苗箱に於て播種の1
週間乃至10日前に(P)を散布し、土とよく混和させ
ておく。
{a) Timing of application of LPN-3 powder IP) 1 week to 10 days before planting seedlings at Honda (P)
Spray and mix well with the soil, then sow seeds in a seedling box.
Spray (P) a week to 10 days in advance and mix well with the soil.

(b)LFN−3液剤血の施用時期 LFN−3液剤!L)は田植を終ったのち散布する(第
1回目)。
(b) Application timing of LFN-3 liquid blood LFN-3 liquid! L) will be sprayed after rice planting is completed (first time).

第1回目散布後、10日後に2回目の散布し更にその1
0日後3回目の散布する。尚、本田の開花時期にもう1
回散布することもある。3.肥料、農薬名は、いづれも
商品名である。
After the first spraying, 10 days later, the second spraying and then the first spraying.
Spray for the third time after 0 days. In addition, there is another one during the flowering period of Honda.
It may be sprayed twice. 3. The names of fertilizers and pesticides are all product names.

4.裁培密度は3.3で当り72株とした。4. The culture density was 3.3, with 72 plants per seed.

この結果、2等米が510k9(8.5俵)得られた。
なお、対照としてこの水田の隣接由において、LFN−
3を使用する以外は全く同様な方法で水稲を栽培したが
、その結果は、品質が非常に劣った4等米が、しかも4
20k9(7俵)しか得られなかつた。従って、LFN
−3によって、顕著な結実増加、品質改良効果の得られ
ることが、はっきりわかるのである。
As a result, 510k9 (8.5 bales) of second grade rice was obtained.
As a control, LFN-
I cultivated paddy rice in exactly the same way except using 3rd grade rice, but the result was 4th grade rice with very poor quality, and even 4 grade rice.
Only 20k9 (7 bales) were obtained. Therefore, LFN
-3 clearly shows that a remarkable increase in fruit set and quality improvement effects can be obtained.

実施例 3 トマトを7年間連作した圃場段に水稲を栽培した後、再
度トマト(抑制大型ズィコウ)を昭和51年11月10
日に定植した。
Example 3 After cultivating paddy rice in a field where tomatoes had been continuously cultivated for 7 years, tomatoes (suppressed large-sized rice plant) were grown again on November 10, 1976.
It was planted on the day.

肥料としては、切りわら200k9、ミネラルフミン7
0k9、齢鶏糞、70k9、ケイ酸マグ30k9、鱗硝
安カリ50k9、カリ8kg、リン15kgを元肥とし
、そして追肥として燐硝安カリ30kgを3回に分施し
た。常法により栽培を継続したが、農薬としてトップジ
ンM、ダイセンを3回づつ施用したにも拘らず、し、ち
よう病、青枯病が多発してこのままでは体耕に到る状態
となった。
As fertilizer, cut straw 200k9, mineral humin 7
0k9, old chicken manure, 70k9, silicate mag 30k9, scale sulfate ammonium 50k9, potash 8 kg, and phosphorus 15 kg were used as base fertilizers, and as additional fertilizer, phosphorus sulfate ammonium potassium 30 kg was applied in three portions. Cultivation continued using conventional methods, but despite applying Topgin M and Daisen three times each as pesticides, rot, mildew, and bacterial wilt occurred frequently, and if left unchecked, it would become necessary to cultivate the crops. .

しかし、この時点で、実施例5のLFN−乳の10M音
液を20クづつ15日間毎日散布し、次に4日おきに藁
面がぬれる程度に葉面散布した。
However, at this point, 20 batches of the 10M sonic solution of LFN-milk of Example 5 was sprayed every day for 15 days, and then sprayed on the leaves every four days to the extent that the straw surface was wet.

その結果、横勢が持ち直し、トマトの収穫が可能となっ
た。このように連作の被害があらわれた圃場ではtもは
やナス科植物の連作は不可能である。
As a result, the situation has improved and tomatoes can now be harvested. In fields where damage from continuous cropping has occurred in this way, it is no longer possible to continuously cultivate solanaceous plants.

しかしながら、LFN処理することにより連作が可能と
なった。
However, continuous cropping became possible by LFN treatment.

すなわち、肥料としては、くみあい尿素入り硫加燐安4
64を2袋(20k9入)を使用し、昭和52王5月2
4日にナス(品種千成)を定植した。なお、元肥として
実施例4で得たLFN一如を30k9使用し「更に、実
施例5で得たLFN一丸の10の音液を4日おきに20
そ/回宛葉面に散布した。昭和53王7月1日から収穫
が可能となり、平均21k9/日のナスの収穫が得られ
、最高値は37k9/日であった。
In other words, as a fertilizer, sulfurized phosphorus ammonium 4 containing urea is used.
Using 2 bags of 64 (20k9 pieces), May 2, 1974
Eggplants (variety Sennari) were planted on the 4th. In addition, 30k9 of LFN Ichinyo obtained in Example 4 was used as a starter fertilizer, and 20k9 of LFN Ichimaru obtained in Example 5 was added every 4 days.
It was sprayed on the leaves each time. Harvesting began on July 1, 1973, and an average yield of eggplants was 21k9/day, with the highest yield being 37k9/day.

9月10日まで収穫があり、全収量は1600kgであ
った。
Harvesting continued until September 10th, with a total yield of 1,600 kg.

途中ダィセンを月2回散布したところ、病虫害の発生は
なかった。
During the process, I sprayed Daisen twice a month, but no pests or diseases occurred.

従って、LFN処理することによって、連作障害を防止
できることがわかる。
Therefore, it can be seen that continuous crop failure can be prevented by performing LFN processing.

実施例 4 参考例1によって製造したLFN−3:7%、N:3%
「K20:19%、貝化石:残量を良く粉砕混合して粉
状のLFN−3(LFN一如)を製造した。
Example 4 LFN-3 manufactured according to Reference Example 1: 7%, N: 3%
"K20: 19%, shellfish fossil: The remaining amount was thoroughly ground and mixed to produce powdered LFN-3 (LFN Ichiro).

この1%溶液は、pHは約8.0を呈する。実施例 5
参考例1によって製造したLFN−3:5%、N:8%
、P24:1%、K20:3%、日20:残量を良く混
合して液状のLFN−3(LFN−丸)を製造した。
This 1% solution exhibits a pH of approximately 8.0. Example 5
LFN-3 manufactured according to Reference Example 1: 5%, N: 8%
, P24: 1%, K20: 3%, Day 20: The remaining amounts were mixed well to produce liquid LFN-3 (LFN-circle).

Claims (1)

【特許請求の範囲】[Claims] 1 四塩化珪素(SiCl_4)、六塩化珪素(Si_
2Cl_6)及び八塩化珪素(Si_3Cl_8)から
なる群から選ばれる珪素の塩化物を予め空気に接触させ
ておき、これに塩化水素ガスを夫々の2%以上共存させ
、これに水素を200℃以上の温度で反応させて液状の
珪水塩化物(HSi_3Cl_7)を得た後、これをガ
ス化させ、水に吸収溶解させ、次いでヒドラジンを反応
させ、そして最後にアルカリを加えて中和して窒素化し
た珪水塩化物(Cl_6Si_3(NH_2)・H)を
得、これを水で稀釈した後、生の全魚体、魚内臓、又は
魚肉を混合して発酵させ、 このようにして得られた発
酵製品を有効成分として含有せしめたこと、を特徴とす
る土壤改良兼植物育成剤。
1 Silicon tetrachloride (SiCl_4), silicon hexachloride (Si_
A silicon chloride selected from the group consisting of silicon chloride (Si_3Cl_6) and silicon octachloride (Si_3Cl_8) is brought into contact with air in advance, hydrogen chloride gas is allowed to coexist with it in an amount of 2% or more of each, and hydrogen is added to this at a temperature of 200°C or higher. After reacting at high temperature to obtain liquid silica chloride (HSi_3Cl_7), it is gasified, absorbed and dissolved in water, then reacted with hydrazine, and finally neutralized by adding alkali to nitrogenize. Diluted silica chloride (Cl_6Si_3(NH_2).H) is obtained, diluted with water, mixed with raw whole fish, fish internal organs, or fish meat, and fermented. A soil improving and plant growing agent characterized by containing as an active ingredient.
JP53139240A 1978-11-10 1978-11-10 A plant breeding agent that improves the physical, chemical, and biological aspects of soil and imparts soil fertility. Expired JPS606319B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP53139240A JPS606319B2 (en) 1978-11-10 1978-11-10 A plant breeding agent that improves the physical, chemical, and biological aspects of soil and imparts soil fertility.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP53139240A JPS606319B2 (en) 1978-11-10 1978-11-10 A plant breeding agent that improves the physical, chemical, and biological aspects of soil and imparts soil fertility.

Publications (2)

Publication Number Publication Date
JPS5565290A JPS5565290A (en) 1980-05-16
JPS606319B2 true JPS606319B2 (en) 1985-02-16

Family

ID=15240723

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JPS606319B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107857632A (en) * 2017-11-01 2018-03-30 侯彦阳 A kind of composition of alternative various plants hormone and preparation method thereof

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