JPH0224241B2 - - Google Patents

Info

Publication number
JPH0224241B2
JPH0224241B2 JP14579782A JP14579782A JPH0224241B2 JP H0224241 B2 JPH0224241 B2 JP H0224241B2 JP 14579782 A JP14579782 A JP 14579782A JP 14579782 A JP14579782 A JP 14579782A JP H0224241 B2 JPH0224241 B2 JP H0224241B2
Authority
JP
Japan
Prior art keywords
water
polymerization
monomer
acrylic acid
aqueous 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
Application number
JP14579782A
Other languages
Japanese (ja)
Other versions
JPS5936601A (en
Inventor
Tooru Myajima
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.)
KYORITSU JUKI KOGYO KENKYUSHO KK
Original Assignee
KYORITSU JUKI KOGYO 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 KYORITSU JUKI KOGYO KENKYUSHO KK filed Critical KYORITSU JUKI KOGYO KENKYUSHO KK
Priority to JP14579782A priority Critical patent/JPS5936601A/en
Publication of JPS5936601A publication Critical patent/JPS5936601A/en
Publication of JPH0224241B2 publication Critical patent/JPH0224241B2/ja
Granted legal-status Critical Current

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  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Polymerisation Methods In General (AREA)

Description

【発明の詳細な説明】 本発明は園芸用持続性薬剤の製造方法に関し、
詳しくは2.5モル量以下の水に溶解したアクリル
酸アンモニウムおよび/またはアクリル酸カリウ
ムの重合を行うにあたり、該モノマー水溶液中に
各種園芸用薬剤を溶解した後、重合を行うことに
より上記添加薬剤を保持したポリマーの乾燥固体
を得る方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a long-acting horticultural drug,
Specifically, when polymerizing ammonium acrylate and/or potassium acrylate dissolved in water in an amount of 2.5 molar or less, various horticultural chemicals are dissolved in the monomer aqueous solution and then polymerized to retain the above additive chemicals. The present invention relates to a method for obtaining a dry solid of a polymer.

従来より園芸用として肥料、殺虫剤、殺菌剤、
ケミカルレギユレーシヨン剤等各種の薬品が使用
されている。例えば、植物に欠くことができない
肥料成分としてのN.P.Kの主要三要素の他、Fe、
Cu、Mn、B、Zn、Moその他の微量元素が必要
であることは広く知られているところである。こ
れらの微量元素は水に不溶性の化合物として施肥
される場合と、水溶性塩の形で施肥される場合が
ある。水溶性塩の方が植物に利用され易い形であ
り、速効性があるが、特に砂質土壌の場合、流亡
し易い欠点があり、水不溶性の場合は流亡は少な
いが利用効率も低い。
Fertilizers, insecticides, fungicides,
Various chemicals such as chemical regulation agents are used. For example, in addition to the three main elements of NPK, which are essential fertilizer components for plants, Fe,
It is widely known that trace elements such as Cu, Mn, B, Zn, Mo and others are necessary. These trace elements may be applied as water-insoluble compounds or in the form of water-soluble salts. Water-soluble salts are easier to use by plants and have a faster effect, but they have the disadvantage of being easily washed away, especially in sandy soils, while water-insoluble salts are less likely to be washed away, but their utilization efficiency is also low.

ところで水溶性塩を安定な水性ゲル粒子中に均
一に分散せしめれば、利用効率を下げることなく
持続性を維持できる。また水性ゲルの粒径を適当
に選ぶことにより溶出速度を調節することも容易
である。
By the way, if the water-soluble salt is uniformly dispersed in stable aqueous gel particles, sustainability can be maintained without lowering utilization efficiency. Furthermore, the elution rate can be easily adjusted by appropriately selecting the particle size of the aqueous gel.

しかし既知の水性ゲルは微生物に対し不安定で
あつたり、工程が複雑でコスト高となる等の欠点
があつた。もし有用成分を含んだ水性ゲルが乾燥
固体の状態で入手できれば、適宜な粒度に粉砕す
ることは容易であり、運搬やその他の取扱の点で
も有利であることは論をまたない。
However, known aqueous gels have drawbacks such as being unstable to microorganisms, requiring complicated processes, and increasing costs. If an aqueous gel containing useful ingredients can be obtained in the form of a dry solid, it is easy to grind it to an appropriate particle size, and it is undoubtedly advantageous in terms of transportation and other handling.

本発明者はこのような条件を種々検討の結果、
有用成分を内部に包含した水膨潤性ポリマー乾燥
固体を簡便に得る方法を案出し、本発明に至つ
た。
As a result of various studies on such conditions, the present inventor found that
The present invention was achieved by devising a method for easily obtaining a dry water-swellable polymer solid containing useful components.

すなわち、本発明はモノマーに対し50〜
20000ppmのジビニル化合物共存下、アクリル酸
中和物の高濃度の水溶液に所望の有用成分を均一
に分散混合した後、重合を行い、重合時発する熱
により水分を気化せしめることにより、乾燥工程
を経ることなく有効成分を包含したポリマー乾燥
固体を得る方法である。
That is, the present invention provides monomers with a
After uniformly dispersing and mixing the desired useful ingredients in a highly concentrated aqueous solution of acrylic acid neutralized product in the coexistence of 20,000 ppm of divinyl compound, polymerization is performed, and the water is vaporized by the heat generated during polymerization, followed by a drying process. This is a method to obtain a dry polymer solid containing the active ingredient without any oxidation.

水分の蒸発に必要な熱の発生はすべてアクリル
酸モノマーの重合熱によるところから、重合に供
するモノマー水溶液中の水分含有量はアクリル酸
モノマーに対して2.5倍モル量以下である必要が
あり、これ以上の水分の共存は重合後のポリマー
含水率が高いため、そのままでは粉砕することが
できない。
Since all of the heat required for evaporation of water is generated by the heat of polymerization of the acrylic acid monomer, the water content in the monomer aqueous solution used for polymerization must be 2.5 times the molar amount or less of the acrylic acid monomer. If water is present in the above manner, the water content of the polymer after polymerization is high, so it cannot be pulverized as it is.

重合に供されるアクリル酸はアンモニウムおよ
び/またはカリウム塩であり、ナトリウム塩は植
物の生育阻害を招くおそれがある。
Acrylic acid subjected to polymerization is ammonium and/or potassium salt, and sodium salt may inhibit plant growth.

モノマー溶液に共存させるジビニル化合物は生
成したアクリル酸ポリマーが水に不溶性となるよ
う架橋剤として用いるものであるが、メチレンビ
スアクリルアミドのような水溶性化合物が望まし
く、ジビニルベンゼンのような油溶性化合物はモ
ノマー水溶液中に均一に分散させることが難かし
い。
The divinyl compound coexisting in the monomer solution is used as a crosslinking agent to make the produced acrylic acid polymer insoluble in water, but a water-soluble compound such as methylenebisacrylamide is preferable, and an oil-soluble compound such as divinylbenzene is preferable. It is difficult to uniformly disperse the monomer in an aqueous solution.

重合開始には、通常のラジカル重合に用いられ
る開始剤であるアゾビスイソブチロニトリル、ア
ゾビスアミジノプロパン、アゾビスイソシアノ吉
草酸等のアゾ化合物および過硫酸水素ナトリウ
ム、過硫酸カリウム等の過硫酸塩を単独に、ある
いは亜硫酸水素ナトリウムのような還元剤を併用
して用いることができる。
To initiate the polymerization, azo compounds such as azobisisobutyronitrile, azobisamidinopropane, and azobisisocyanovaleric acid, which are initiators used in normal radical polymerization, and peroxidants such as sodium hydrogen persulfate and potassium persulfate are used. Sulfates can be used alone or in combination with reducing agents such as sodium bisulfite.

重合時発熱する水蒸気の発散に便ならしめるた
め、重合容器の上部は開放している必要があり、
エンドレスベルト上で重合することが望ましい。
The top of the polymerization container must be open to vent the water vapor generated during polymerization.
It is desirable to polymerize on an endless belt.

モノマー水溶液中に共存させる有用物質は先に
例示した微量元素のみにとどまることなく、モノ
マー水溶液中に均一に分散させることができ、重
合後、ポリマー中にとどまるものであれば、すべ
ての化学薬品に適用できることはいうまでもな
い。
Useful substances to coexist in the monomer aqueous solution are not limited to the trace elements listed above, but can be used for all chemicals as long as they can be uniformly dispersed in the monomer aqueous solution and remain in the polymer after polymerization. Needless to say, it is applicable.

以下、実施例により本発明を具体的に説明する
が、本発明はその要旨を超えないかぎり以下述べ
る実施例に制約されるものではない。
Hereinafter, the present invention will be specifically explained with reference to Examples, but the present invention is not limited to the Examples described below unless it exceeds the gist thereof.

実施例 1 アクリル酸72gを300mlガラスビーカーに採取
し、50℃以下に冷却しながら25%アンモニア水40
gを混合し、中和する。つぎに炭酸カリウム14g
を脱泡しながら徐々に加え、さらにメチレンビス
アクリルアミド700mg、モリブデン酸アンモニウ
ム10mg、ニコチン硫酸塩100mgを加えて均一に混
合する。温度を40℃に調節する。その後アゾビス
アミジノプロパン塩酸塩700mgを添加混合し、直
ちに70℃の水浴上に保持した。面積100cm2のテフ
ロンコーテイング浅皿上に移し替え、重合させ
る。
Example 1 Collect 72 g of acrylic acid in a 300 ml glass beaker, and add 40 g of 25% ammonia water while cooling to below 50°C.
Mix and neutralize. Next, 14g of potassium carbonate
While defoaming, gradually add 700 mg of methylene bisacrylamide, 10 mg of ammonium molybdate, and 100 mg of nicotine sulfate, and mix uniformly. Adjust temperature to 40°C. Thereafter, 700 mg of azobisamidinopropane hydrochloride was added and mixed, and the mixture was immediately kept on a 70°C water bath. Transfer to a Teflon-coated shallow dish with an area of 100 cm 2 and allow to polymerize.

水蒸気が出なくなつてから3分後、容器から取
出し、冷却後粉砕する。標準フルイにて40〜60メ
ツシユにて篩別した粉末を試料1とする。
3 minutes after water vapor stops coming out, take it out from the container, cool it, and crush it. Sample 1 is a powder sieved with 40 to 60 meshes using a standard sieve.

同様の操作によりニコチン硫酸塩を含まぬ以外
は試料1と同様に製造した粉末を試料2とした。
Sample 2 was a powder produced in the same manner as Sample 1 except that it did not contain nicotine sulfate.

効果試験 砂質土壌である相模川岸の畑土を各2Kgずつ充
分の大きさのポツトに分取した。試験区用として
各5個ずつになるようにランダムにポツトを区分
けして、試験区には試料1を、対象区には試料2
を各々1ポツトにつき2gずつ添加均一に混合し
た。対に1リツトルずつ撒布した。
Efficacy test 2 kg of sandy field soil from the banks of the Sagami River was divided into pots of sufficient size. Randomly divide the pots into 5 pots each for the test plots, and place sample 1 in the test plot and sample 2 in the target plot.
2 g of each was added to each pot and mixed uniformly. 1 liter was applied to each pair.

対象区には水道水1リツトルずつを撒水した。 One liter of tap water was sprinkled on each target area.

1週間後、なす苗を1ポツトに1本ずつ定植
し、その後の状態を観察した。
One week later, one eggplant seedling was planted in each pot, and the condition thereafter was observed.

対象区には、2週間以内に全株にアリマキが寄
生したのに対し、試験区では収穫に至るまで虫害
は全く認められなかつた。
In the target plot, all the plants were infested with aphids within two weeks, whereas in the test plot, no insect damage was observed at all until harvest.

Claims (1)

【特許請求の範囲】[Claims] 1 ジビニル化合物共存下、モノマーに対し2.5
倍モル量以下の水を含有するアクリル酸のアンモ
ニウムおよび/またはカリウム中和物水溶液中に
有用成分を均一に分散させた後、重合せしめ、そ
の重合熱によつて水を気化せしめることにより、
乾燥工程を経ることなく粉砕可能なポリマー乾燥
固体を得ることを特徴とする園芸用持続性薬剤の
製造方法。
1 2.5 to monomer in the presence of divinyl compound
By uniformly dispersing the useful ingredient in an aqueous solution of ammonium and/or potassium neutralized acrylic acid containing up to twice the molar amount of water, and then polymerizing it and vaporizing the water with the heat of polymerization,
A method for producing a long-lasting horticultural agent, characterized by obtaining a dry polymer solid that can be crushed without undergoing a drying process.
JP14579782A 1982-08-23 1982-08-23 Preparation of horticultural prolonged release type chemical Granted JPS5936601A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14579782A JPS5936601A (en) 1982-08-23 1982-08-23 Preparation of horticultural prolonged release type chemical

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14579782A JPS5936601A (en) 1982-08-23 1982-08-23 Preparation of horticultural prolonged release type chemical

Publications (2)

Publication Number Publication Date
JPS5936601A JPS5936601A (en) 1984-02-28
JPH0224241B2 true JPH0224241B2 (en) 1990-05-29

Family

ID=15393368

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14579782A Granted JPS5936601A (en) 1982-08-23 1982-08-23 Preparation of horticultural prolonged release type chemical

Country Status (1)

Country Link
JP (1) JPS5936601A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH055995U (en) * 1991-07-10 1993-01-29 住友ゴム工業株式会社 Trowel for resin coating floor work
JP2544742Y2 (en) * 1991-12-27 1997-08-20 住友ゴム工業株式会社 Rotating trowel
JP2009523152A (en) * 2006-01-12 2009-06-18 ビーエーエスエフ ソシエタス・ヨーロピア Agrochemical formulation based on molecularly imprinted acrylate

Also Published As

Publication number Publication date
JPS5936601A (en) 1984-02-28

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