KR20000028283A - Microcapsule insecticide using biodegradable polymeric material - Google Patents

Microcapsule insecticide using biodegradable polymeric material Download PDF

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Publication number
KR20000028283A
KR20000028283A KR1019980046456A KR19980046456A KR20000028283A KR 20000028283 A KR20000028283 A KR 20000028283A KR 1019980046456 A KR1019980046456 A KR 1019980046456A KR 19980046456 A KR19980046456 A KR 19980046456A KR 20000028283 A KR20000028283 A KR 20000028283A
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South Korea
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insecticide
polylactic acid
dissolved
added
micro capsule
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KR1019980046456A
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Korean (ko)
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장봉석
김노수
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안민동
국보제약 주식회사
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Priority to KR1019980046456A priority Critical patent/KR20000028283A/en
Publication of KR20000028283A publication Critical patent/KR20000028283A/en

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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/26Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests in coated particulate form
    • A01N25/28Microcapsules or nanocapsules
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A01N25/04Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/12Powders or granules
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/36Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N53/00Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N57/00Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/12Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N57/00Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/14Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing aromatic radicals
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N57/00Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/16Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L101/00Compositions of unspecified macromolecular compounds
    • C08L101/16Compositions of unspecified macromolecular compounds the macromolecular compounds being biodegradable
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N2300/00Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48

Abstract

PURPOSE: A micro capsule insecticide capsuled an insecticidal composition with a biodegradable polymer is provided which is effective in reducing effort and cost by spraying of chemicals because of the gradually releasing property of chemical component. CONSTITUTION: A biodegradable micro capsule insecticide comprises as an active component organic phosphorus insecticides or pyrethroid insecticides, organic solvents, poly lactic acid as a capsuling agent and one or more of supplement agents selected from the groups consisting of surface active agents, dispersing agents, viscosity controllers, and water. Also described is a dispersion liquid phase type micro capsule insecticide or powdery type micro capsule insecticide.

Description

생분해성 고분자 물질을 이용한 마이크로캡슐 형태의 살충제Microcapsule Insecticide Using Biodegradable Polymer

본 발명은 생분해성 고분자를 이용한 마이크로캡슐 형태의 살충제에 관한 것이다.The present invention relates to a microcapsule type insecticide using a biodegradable polymer.

환경오염의 문제는 더 이상 방치할 수 없는 지구 전체와 인류생존의 문제이다. 많은 환경오염의 원인 중 하나는 필요 이상의 과다한 양의 농약 및 살충제의 사용이라고 할 수 있다. 농약 및 살충제의 무분별한 사용으로 인하여 꼭 박멸해야 할 해충뿐 아니라, 유해하지 않거나 혹은 유익한 곤충마저도 죽이게되는 결과를 초래하게 된다. 그리하여 그 곤총들을 먹이로 하는 조류 및 동물들의 먹이사슬을 끊어서 생태계에도 치명적인 악영향을 미치게 된다.The problem of environmental pollution is the problem of the whole planet and human survival that can no longer be neglected. One of the causes of many environmental pollutions is the use of excess pesticides and pesticides. Indiscriminate use of pesticides and pesticides results in the killing of not only harmful pests but also harmful or beneficial insects. Thus, the food chains of the birds and animals that feed them are cut off, and the ecosystem is devastating.

본 발명자들은 이러한 환경문제에 영향을 미치지 않으면서 인류에 해로운 해충들을 퇴치하기 위하여 노력한 결과, 살충제 성분을 마이크로캡슐형태로 제조하는 방법을 개발하여 본 발명을 완성하였다.The present inventors have endeavored to combat pests harmful to humans without affecting these environmental problems, and thus, the present invention has been completed by developing a method for preparing pesticide components in the form of microcapsules.

본 발명에 따른 마이크로캡슐화된 살충제는 환경에 노출되어도 환경오염이 전혀 없는 생분해성 물질을 이용하여 살충제 성분을 캡슐화 물질로 감싸서 강한 독성을 완화시키고 캡슐물질이 서서히 분해 되면서 캡슐화된 살충제 약제 성분이 지속적으로 서서히 방출되므로 살충제의 살포 횟수 및 살포량을 줄이게 되어 약제살포로 인한 자연환경 오염과 약제살포에 대한 노력과 비용을 줄일 수 있다.The microencapsulated insecticide according to the present invention uses a biodegradable substance that is not environmentally polluted even when exposed to the environment to alleviate strong toxicity by encapsulating the insecticide component with the encapsulating substance and continuously encapsulate the encapsulated insecticide pharmaceutical ingredient as the encapsulating substance is gradually degraded. Since it is released slowly, the number of sprays and the amount of spraying of pesticides can be reduced, thereby reducing the environmental pollution caused by drug spraying and the effort and cost of drug spraying.

살충제 물질을 캡슐화 하는 목적은 약효지속 효과가 짧은 약제들의 약효지속 기간을 연장시킬 수 있으며, 독성이 강한 살충제 성분을 캡슐물질로 감싸서 서서히 방출하게 되므로 강한 독성을 완화시키는 데 있다. 또한 살충제를 캡슐화 함으로써 살충제의 남용을 최소화 할 수 있게 되고 해충들에게 치명적으로 작용하지만 기타 먹이사슬관계에 있는 조류나 동물들에게는 치명적인 영향을 주지 않는 장점이 있다.The purpose of encapsulating the pesticide material is to extend the drug duration of drugs with short duration of drug efficacy, and to relieve strong toxicity because it is slowly released by encapsulating the toxic pesticide ingredient in a capsule material. In addition, by encapsulating the pesticide, it is possible to minimize the abuse of the pesticide and to act deadly to pests, but it does not have a fatal effect on other birds or animals in the food chain relationship.

따라서, 본 발명의 목적은 살충제 성분을 생분해 물질로 감싸서 제조하는 마이크로 캡슐형태의 살충제를 제공하는 것이다.Accordingly, it is an object of the present invention to provide a microcapsule-type pesticide prepared by wrapping the pesticide component with a biodegradable material.

본 발명의 또다른 목적은 살충제 성분을 생분해 물질로 감싸서 제조하는 마이크로 캡슐형태의 살충제를 현탁액이나 분말제제를 제공하는 것이다.It is another object of the present invention to provide a suspension or powder formulation of a pesticide in microcapsule form prepared by wrapping the pesticide component with a biodegradable substance.

본 발명은 생분해성 고분자인 PLA(Poly Lactic Acid)를 캡슐화벽 물질로 사용하여 현재 전세계적으로 사용되고 있는 유기인계 살충제인 클로르피리포스, 디클로르보스, 훼니트로치온, 다이아지논등과 합성 피레스로이드계 살충제인 델타메쓰린, 싸이퍼메쓰린, 퍼메쓰린 등을 마이크로캡슐화 상태로 만들게 되었다.The present invention is a synthetic pyrethroid using PLA (Poly Lactic Acid), a biodegradable polymer, as an encapsulating wall material and organophosphorus insecticides such as chlorpyriphos, dichlorbose, fenitrothion, diazinon, etc. Insecticides deltamethrin, ciphermethrin, and permethrin have been microencapsulated.

마이크로캡슐화 살충제의 제조방법을 간단히 설명하면 유기인계 살충성분과 합성 피레스로이드계 살충성분을 유기용제에 용해시킨 다음 계면활성제, 분산제, 점도조절제, 물 등을 첨가한다. 상기 용액을 폴리락산을 아세톤의 중량비로 1 대 1 내지 1 대 10의 비율로 용해시킨 용액에 격렬히 교반시켜주면서 첨가하여 마이크로캡슐화 살충제를 제조한다.Briefly describing the preparation method of the microencapsulated insecticide, the organophosphorus insecticide and the synthetic pyrethroid insecticide are dissolved in an organic solvent, and then a surfactant, a dispersant, a viscosity modifier, and water are added. The solution is added to the solution in which polylactic acid is dissolved in a ratio of 1 to 1 to 10 in a weight ratio of acetone while being vigorously stirred to prepare a microencapsulated insecticide.

마이크로캡슐화 살충제의 분말제제의 제조방법을 간단히 설명하면, 유기인계 살충성분과 합성 피레스로이드계 살충성분을 유기용제에 용해시킨 다음 계면활성제, 분산제, 물 등을 첨가한다. 상기 용액을 폴리락산을 아세톤의 중량비로 1대 1 내지 1 대 10의 비율로 용해시킨 용액에 격렬히 교반시켜 주면서 첨가한 다음 이 용액을 여과, 건조시켜 마이크로캡슐화된 분말제를 제조한다.A brief description will be made of a method for preparing a microencapsulated insecticide powder, in which an organic phosphorus insecticide component and a synthetic pyrethroid insecticide component are dissolved in an organic solvent, and then a surfactant, a dispersant, and water are added. The solution is added to the solution in which polylactic acid is dissolved in a ratio of 1 to 1 to 10 in a weight ratio of acetone with vigorous stirring, and then the solution is filtered and dried to prepare a microencapsulated powder.

본 발명에서 사용된 유기인계 살충제들은 클로르피리포스, 다이아지논, 디클로르보스, 훼니트로치온 등이며, 합성 피레스로이드계 살충제들은 델타메스린, 싸이퍼메스린, 퍼메스린 등이다. 이들 살충성분을 중량비로 1내지 80 퍼센트를 캡슐화 하여 사용하였으며, 비이온성 계면활성제로는 TWEEN 80(상품명), MONOPOL(상품명), 폴리옥시알킬렌 아릴에테르(Polyoxyalkylene arylether), 소르비탄 모노에스테르(Sorbitan monoester) 등을 사용할 수 있으며, 양이온성 계면활성제로는 Pionnin SB50(상품명), 음이온성 계면활성제로는 소디움 도데실 설페이트, 알킬 벤젠 설폰네이트 등을 중량비로 3 내지 20퍼센트를 사용하였다.Organophosphorus insecticides used in the present invention are chlorpyriphos, diazinon, dichlorbose, fenitrothion and the like, and synthetic pyrethroid insecticides are deltamethrin, cyspermethrin, permethrin and the like. These insecticides were encapsulated in a weight ratio of 1 to 80 percent, and nonionic surfactants were TWEEN 80 (trade name), MONOPOL (trade name), polyoxyalkylene arylether, and sorbitan monoester (Sorbitan). monoester) and Pionnin SB50 (trade name) as the cationic surfactant, sodium dodecyl sulfate, alkyl benzene sulfonate and the like by weight of 3 to 20% as anionic surfactant.

분산제로는 NK-KNZ(상품명)(Epoxidized fatty oil), NK-DIS(상품명) 20(alkyl naphthalene sulfonate, lignosulfonate mixture), 잔탄검 등을 중량비로 1 내지 10퍼센트를 사용하였으며 점도조절제로는 글리세린, 프로필렌 글리콜 등을 중량비로 5 내지 20 퍼센트를 사용하였으며, 유기용제로는 Solvesso(상품명), Kocosol(상품명), 디아세톤 알콜(Diacetone alcohol), 아세톤, 메틸렌 클로라이드 등을 중량비로 0 내지 30 퍼센트를 사용하였다.As dispersant, NK-KNZ (Epoxidized fatty oil), NK-DIS (trade name) 20 (alkyl naphthalene sulfonate, lignosulfonate mixture), xanthan gum, etc. were used in a weight ratio of 1 to 10 percent. 5 to 20 percent by weight of propylene glycol was used, and organic solvents used were 0 to 30 percent by weight of Solvesso (trade name), Kocosol (trade name), diacetone alcohol, acetone, methylene chloride, and the like. It was.

본 발명을 다음의 실시예에서 자세히 설명하지만 다음의 실시예로 본 발명이 한정되는 것은 아니다.The invention is described in detail in the following examples, but the invention is not limited to the following examples.

실시예 1Example 1

고속교반 장치와 환류냉각기가 부착된 반응기에 클로르피리포스 100g, 아세톤 100g, 폴리락산 20g을 넣고 가열하여 환류냉각 하면서 서서히 교반하여 용해시킨다.모두다 용해되면 이용액에 계면활성제인 소디움 도데실 설페이트(Sodium dodecyl sulfate) 10g과 잔탄검 2g을 물 698g에 용해시킨 수용액을 천천히 첨가하면서 교반회전을 증가시켜 분당 회전수 3,000회전을 유지한다. 계속하여 NK-KNZ(상품명) 20g, 글리세린 50g을 넣고 2시간동안 고속으로 회전하여 평균입경이 10내지 100미크론의 폴리락산으로 캡슐화된 클로르피리포스 10%현탁액 1,000g을 얻었다.In a reactor equipped with a high speed stirrer and a reflux condenser, 100 g of chlorpyriphos, 100 g of acetone, and 20 g of polylactic acid are added, heated, and refluxed. The solution is slowly stirred and dissolved. When all are dissolved, sodium dodecyl sulfate as a surfactant is used in the solution. Slowly add the aqueous solution in which 10 g of dodecyl sulfate) and 2 g of xanthan gum were dissolved in 698 g of water, increasing the stirring rotation to maintain 3,000 revolutions per minute. Subsequently, 20 g of NK-KNZ (trade name) and 50 g of glycerin were added and rotated at a high speed for 2 hours to obtain 1,000 g of chlorpyriphos 10% suspension encapsulated with polylactic acid having an average particle diameter of 10 to 100 microns.

실시예 2Example 2

고속교반 장치와 환류냉각기가 부착된 반응기에 다이아지논 100g, 디아세톤 알코올(Diacetone alcohol) 100g, 폴리락산(Polylactic acid) 20g을 넣고 가열하여 환류냉각 하면서 서서히 교반하여 용해 시킨다. 모두다 용해되면 이 용액에 계면활성제인 폴리옥시알킬렌 아릴에테르 10g과 잔탄검 2g을 물 698g에 용해시킨 수용액을 천천히 첨가하면서 교반회전을 증가시켜 분당 회전수 3,000회전을 유지한다. 계속하여 NK-KNZ(상품명) 20g, 플로필렌 글리콜 50g을 넣고 2시간동안 고속으로 회전하여 평균입경이 10내지 100미크론의 폴리락산으로 캡슐화된 다이아지논 10% 현탁액 1,000g을 얻었다.100 g of diazinon, 100 g of diacetone alcohol, and 20 g of polylactic acid were added to a reactor equipped with a high speed stirring device and a reflux cooler, and the mixture was heated to reflux and slowly stirred to dissolve. When all are dissolved, an aqueous solution of 10 g of polyoxyalkylene aryl ether and 2 g of xanthan gum, dissolved in 698 g of water, is slowly added to the solution to increase stirring and maintain 3,000 revolutions per minute. Subsequently, 20 g of NK-KNZ (trade name) and 50 g of flohylene glycol were added thereto, and the mixture was rotated at high speed for 2 hours to obtain 1,000 g of a diazinon 10% suspension encapsulated with polylactic acid having an average particle diameter of 10 to 100 microns.

실시예 3Example 3

고속교반 장치와 환류냉각기가 부착된 반응기에 델타메쓰린 100g, Solvesso(상품명) 100g, 폴리락산 20g을 넣고 가열하여 환류냉각 하면서 서서히 교반하여 용해 시킨다. 모두다 용해되면 이 용액에 계면활성제인 소디움 도데실 설페이트(Sodium dodecyl sulfate) 10g과 잔탄검 2g을 물 698g에 용해시킨 수용액을 천천히 첨가하면서 교반회전을 증가시켜 분당 회전수 3,000회전을 유지한다. 계속하여 NK-KNZ(상품명) 20g, 글리세린 50g을 넣고 2시간동안 고속으로 회전하여 평균입경이 10내지 100미크론의 폴리락산으로 캡슐화된 델타메쓰린 10% 현탁액 1,000g을 얻었다.100 g of deltamethrin, 100 g of Solvesso (trade name), and 20 g of polylactic acid were added to a reactor equipped with a high speed stirring device and a reflux cooler, followed by heating and reflux cooling. When all are dissolved, the solution is slowly added with an aqueous solution of 10 g of sodium dodecyl sulfate and 2 g of xanthan gum in 698 g of water. The stirring speed is increased to maintain 3,000 revolutions per minute. Subsequently, 20 g of NK-KNZ (trade name) and 50 g of glycerin were added and rotated at a high speed for 2 hours to obtain 1,000 g of a deltamethrin 10% suspension encapsulated with polylactic acid having an average particle diameter of 10 to 100 microns.

실시예 4Example 4

고속교반 장치와 환류냉각기가 부착된 반응기에 퍼메쓰린 100g, 아세톤 100g, 폴리락산 20g을 넣고 가열하여 환류냉각 하면서 서서히 교반하여 용해 시킨다. 모두다 용해되면 이 용액에 계면활성제인 소디움 도데실 설페이트 10g과 잔탄검 2g을 물 698g에 용해시킨 수용액을 천천히 첨가하면서 교반회전을 증가시켜 분당 회전수 3,000회전을 유지한다. 계속하여 NK-KNZ(상품명) 20g, 글리세린 50g을 넣고 2시간동안 고속으로 회전하여 평균입경이 10내지 100미크론의 폴리락산으로 캡슐화된 퍼메쓰린 10% 현탁액 1,000g을 얻었다.Into a reactor equipped with a high speed stirrer and a reflux condenser, 100 ml of permethrin, 100 g of acetone, and 20 g of polylactic acid were added, heated, and refluxed. When all are dissolved, slowly add an aqueous solution in which 10 g of sodium dodecyl sulfate and 2 g of xanthan gum are dissolved in 698 g of water to the solution to increase the stirring rotation to maintain 3,000 revolutions per minute. Subsequently, 20 g of NK-KNZ (trade name) and 50 g of glycerin were added and rotated at high speed for 2 hours to obtain 1,000 g of a permethrin 10% suspension encapsulated with polylactic acid having an average particle diameter of 10 to 100 microns.

실시예 5Example 5

고속교반 장치와 환류냉각기가 부착된 반응기에 훼니트로치온 100g, Kocosol(상품명) 100g, 폴리락산 20g을 넣고 가열하여 환류냉각 하면서 서서히 교반하여 용해 시킨다. 모두다 용해되면 이 용액에 계면활성제인 소디움 도데실 설페이트 10g과 잔탄검 2g을 물 698g에 용해시킨 수용액을 천천히 첨가하면서 교반회전을 증가시켜 분당 회전수 3,000회전을 유지한다. 계속하여 NK-KNZ(상품명) 20g, 글리세린 50g을 넣고 2시간동안 고속으로 회전하여 평균입경이 10내지 100미크론의 폴리락산으로 캡슐화된 훼니트로치온 10% 현탁액 1,000g을 얻었다.Into a reactor equipped with a high speed stirrer and a reflux condenser, 100 g of fenitrothion, 100 g of Kocosol (trade name), and 20 g of polylactic acid are heated and refluxed while stirring to dissolve gradually. When all are dissolved, slowly add an aqueous solution in which 10 g of sodium dodecyl sulfate and 2 g of xanthan gum are dissolved in 698 g of water to the solution to increase the stirring rotation to maintain 3,000 revolutions per minute. Subsequently, 20 g of NK-KNZ (trade name) and 50 g of glycerin were added and rotated at a high speed for 2 hours to obtain 1,000 g of fenitrothion 10% suspension encapsulated with polylactic acid having an average particle diameter of 10 to 100 microns.

실시예 6Example 6

고속교반 장치와 환류냉각기가 부착된 반응기에 싸이퍼메쓰린 100g, 메틸렌 클로라이드 100g, 폴리락산 20g을 넣고 가열하여 환류냉각 하면서 서서히 교반하여 용해 시킨다. 모두다 용해되면 이 용액에 계면활성제인 소디움 도데실 설페이트 10g과 잔탄검 2g을 물 698g에 용해시킨 수용액을 천천히 첨가하면서 교반회전을 증가시켜 분당 회전수 3,000회전을 유지한다. 계속하여 NK-KNZ(상품명) 20g, 글리세린 50g을 넣고 2시간동안 고속으로 회전하여 평균입경이 10내지 100미크론의 폴리락산으로 캡슐화된 싸이퍼메쓰린 10% 현탁액 1,000g을 얻었다.Into a reactor equipped with a high speed stirrer and a reflux cooler, 100 g of cyphermethrin, 100 g of methylene chloride, and 20 g of polylactic acid are added thereto, heated to reflux, and then slowly stirred to dissolve. When all are dissolved, slowly add an aqueous solution in which 10 g of sodium dodecyl sulfate and 2 g of xanthan gum are dissolved in 698 g of water to the solution to increase the stirring rotation to maintain 3,000 revolutions per minute. Subsequently, 20 g of NK-KNZ (trade name) and 50 g of glycerin were added and rotated at a high speed for 2 hours to obtain 1,000 g of a ciphermethrin 10% suspension encapsulated with polylactic acid having an average particle diameter of 10 to 100 microns.

실시예 7Example 7

고속교반 장치와 환류냉각기가 부착된 반응기에 디클로르보스 100g, 아세톤 100g, 폴리락산 20g을 넣고 가열하여 환류냉각 하면서 서서히 교반하여 용해 시킨다. 모두다 용해되면 이 용액에 계면활성제인 Monopol(상품명) 10g과 NK-DIS20(상품명) 2g을 물 698g에 용해시킨 수용액을 천천히 첨가하면서 교반회전을 증가시켜 분당 회전수 3,000회전을 유지한다. 계속하여 NK-KNZ(상품명) 20g, 글리세린 50g을 넣고 2시간동안 고속으로 회전하여 평균입경이 10내지 100미크론의 폴리락산으로 캡슐화된 디클로르보스 10% 현탁액 1,000g을 얻었다.Into a reactor equipped with a high speed stirrer and a reflux condenser, 100 g of dichloose, 100 g of acetone, and 20 g of polylactic acid were added thereto, heated to reflux, and then slowly stirred to dissolve. When all are dissolved, slowly add an aqueous solution of 10g of Monopol (trade name) and 2g of NK-DIS20 (trade name) to 698g of water, and increase the stirring speed to maintain 3,000 revolutions per minute. Subsequently, 20 g of NK-KNZ (trade name) and 50 g of glycerin were added thereto, and the mixture was rotated at high speed for 2 hours to obtain 1,000 g of a dichlorbose 10% suspension encapsulated with polylactic acid having an average particle diameter of 10 to 100 microns.

실시예 8Example 8

고속교반 장치와 환류냉각기가 부착된 반응기에 클로르피리포스 1,000g, 아세톤 500g, 폴리락산 200g을 넣고 가열하여 환류냉각 하면서 서서히 교반하여 용해 시킨다. 모두다 용해되면 이 용액에 계면활성제인 소디움 도데실 설페이트 100g과 잔탄검 20g을 물 3,000g에 용해시킨 수용액을 천천히 첨가하면서 교반회전을 증가시켜 분당 회전수 3,000회전을 4시간동안 유지한다. 원심분리기에서 탈수시킨 다음 건조 하면 평균입경이 10내지 100미크론의 폴리락산으로 캡슐화된 클로르피리포스 75% 분말제제 1,320g을 얻었다.Into a reactor equipped with a high speed stirring device and a reflux cooler, chlorpyruphos 1,000g, acetone 500g, and polylactic acid 200g were added, heated to reflux cooling, and then slowly stirred to dissolve. When all were dissolved, the solution was slowly added with an aqueous solution of 100 g of sodium dodecyl sulfate and 20 g of xanthan gum in 3,000 g of water, increasing the stirring rotation to maintain 3,000 revolutions per minute for 4 hours. After dehydration in a centrifuge and dried, 1,320 g of chlorpyriphos 75% powder was encapsulated with polylactic acid having an average particle diameter of 10 to 100 microns.

실시예 9Example 9

고속교반 장치와 환류냉각기가 부착된 반응기에 다이아지논 1,000g, 디아세톤 알코올 100g, 폴리락산 200g을 넣고 가열하여 환류냉각 하면서 서서히 교반하여 용해 시킨다. 모두다 용해되면 이 용액에 분산제인 NK-DIS20(상품명) 100g과 잔탄검 20g을 물 3,000g에 용해시킨 수용액을 천천히 첨가하면서 교반회전을 증가시켜 분당 회전수 3,000회전을 6시간동안 유지한다. 원심분리기에서 탈수시킨 다음 건조 하면 평균입경이 10내지 100미크론의 폴리락산으로 캡슐화된 다이아지논 80% 분말제제 1,250g을 얻었다.1,000 g of diazinone, 100 g of diacetone alcohol, and 200 g of polylactic acid were added to a reactor equipped with a high speed stirring device and a reflux condenser, followed by heating, reflux cooling, and agitation. When all are dissolved, slowly add an aqueous solution in which 100 g of NK-DIS20 (trade name) and 20 g of xanthan gum are dissolved in 3,000 g of water. The stirring speed is increased to maintain 3,000 revolutions per minute for 6 hours. After dehydration in a centrifuge and dried, 1,250 g of diazinon 80% powder was encapsulated with polylactic acid having an average particle diameter of 10 to 100 microns.

실시예 10Example 10

고속교반 장치와 환류냉각기가 부착된 반응기에 델타메쓰린 800g, Solvesso 1,000g, 폴리락산 200g을 넣고 가열하여 환류냉각 하면서 서서히 교반하여 용해 시킨다. 모두다 용해되면 이 용액에 계면활성제인 소디움 도데실 설페이트 100g과 잔탄검 20g을 물 3,000g에 용해시킨 수용액을 천천히 첨가하면서 교반회전을 증가시켜 분당 회전수 3,000회전을 4시간동안 유지한다. 원심분리기에서 탈수시킨 다음 건조 하면 평균입경이 10내지 100미크론의 폴리락산으로 캡슐화된 델타메쓰린 70% 분말제제 1,120g을 얻었다.Into a reactor equipped with a high speed stirrer and a reflux condenser, 800 g of deltamethrin, 1,000 g of Solvesso, and 200 g of polylactic acid were added, heated, and refluxed. When all were dissolved, the solution was slowly added with an aqueous solution of 100 g of sodium dodecyl sulfate and 20 g of xanthan gum in 3,000 g of water, increasing the stirring rotation to maintain 3,000 revolutions per minute for 4 hours. When dehydrated in a centrifuge and dried to obtain 1120 g of deltamethrin 70% powder encapsulated with polylactic acid having an average particle diameter of 10 to 100 microns.

실시예 11Example 11

고속교반 장치와 환류냉각기가 부착된 반응기에 퍼메쓰린 800g, 아세톤 500g, 폴리락산 200g을 넣고 가열하여 환류냉각 하면서 서서히 교반하여 용해 시킨다. 모두다 용해되면 이 용액에 계면활성제인 소디움 도데실 설페이트 100g과 잔탄검 20g을 물 3,000g에 용해시킨 수용액을 천천히 첨가하면서 교반회전을 증가시켜 분당 회전수 3,000회전을 6시간동안 유지한다. 원심분리기에서 탈수시킨 다음 건조 하면 평균입경이 10내지 100미크론의 폴리락산으로 캡슐화된 퍼메쓰린 70% 분말제제 1,120g을 얻었다.Into a reactor equipped with a high speed stirrer and a reflux condenser, 800 ml of permethrin, 500 g of acetone, and 200 g of polylactic acid were added, heated, and refluxed. When all were dissolved, the solution was slowly added with an aqueous solution in which 100 g of sodium dodecyl sulfate and 20 g of xanthan gum were dissolved in 3,000 g of water, and the stirring was increased to maintain 3,000 revolutions per minute for 6 hours. When dehydrated in a centrifuge and dried to obtain 1,120 g of a permethrin 70% powder formulation encapsulated with polylactic acid having an average particle diameter of 10 to 100 microns.

실시예 12Example 12

고속교반 장치와 환류냉각기가 부착된 반응기에 훼니트로치온 1,000g, Kocosol 500g, 폴리락산 200g을 넣고 가열하여 환류냉각 하면서 서서히 교반하여 용해 시킨다. 모두다 용해되면 이 용액에 계면활성제인 소디움 도데실 설페이트 100g과 잔탄검 20g을 물 3,000g에 용해시킨 수용액을 천천히 첨가하면서 교반회전을 증가시켜 분당 회전수 3,000회전을 6시간동안 유지한다. 원심분리기에서 탈수시킨 다음 건조 하면 평균입경이 10내지 100미크론의 폴리락산으로 캡슐화된 훼니트로치온 75% 분말제제 1,320g을 얻었다.Into a reactor equipped with a high speed stirrer and a reflux cooler, phenyltrotion 1,000g, 500 g Kocosol, and 200 g polylactic acid were added and heated to reflux and slowly stirred to dissolve. When all were dissolved, the solution was slowly added with an aqueous solution in which 100 g of sodium dodecyl sulfate and 20 g of xanthan gum were dissolved in 3,000 g of water, and the stirring was increased to maintain 3,000 revolutions per minute for 6 hours. When dehydrated in a centrifuge and dried to obtain 1,320 g of phenytrothion 75% powder encapsulated with polylactic acid having an average particle diameter of 10 to 100 microns.

실시예 13Example 13

고속교반 장치와 환류냉각기가 부착된 반응기에 싸이퍼메쓰린 1,000g, 메틸렌 클로라이드 400g, 폴리락산 200g을 넣고 가열하여 환류냉각 하면서 서서히 교반하여 용해 시킨다. 모두다 용해되면 이 용액에 계면활성제인 소디움 도데실 설페이트 100g과 잔탄검 20g을 물 3,000g에 용해시킨 수용액을 천천히 첨가하면서 교반회전을 증가시켜 분당 회전수 3,000회전을 6시간동안 유지한다. 원심분리기에서 탈수시킨 다음 건조 하면 평균입경이 10내지 100미크론의 폴리락산으로 캡슐화된 싸이퍼메쓰린 75% 분말제제 1,320g을 얻었다.Into a reactor equipped with a high speed stirring device and a reflux condenser, 1,000 g of cyphermethrin, 400 g of methylene chloride, and 200 g of polylactic acid were added thereto, followed by heating and reflux cooling. When all were dissolved, the solution was slowly added with an aqueous solution in which 100 g of sodium dodecyl sulfate and 20 g of xanthan gum were dissolved in 3,000 g of water, and the stirring was increased to maintain 3,000 revolutions per minute for 6 hours. When dehydrated in a centrifuge and dried to obtain 1,320 g of Cypermethrin 75% powder encapsulated with polylactic acid having an average particle diameter of 10 to 100 microns.

실시예 14Example 14

고속교반 장치와 환류냉각기가 부착된 반응기에 디클로르보스 800g, 아세톤 200g, 폴리락산 200g을 넣고 가열하여 환류냉각 하면서 서서히 교반하여 용해 시킨다. 모두다 용해되면 이 용액에 계면활성제인 Monopol 100g과 NK-DIS20 50g을 물 3,000g에 용해시킨 수용액을 천천히 첨가하면서 교반회전을 증가시켜 분당 회전수 3,000회전을 6시간동안 유지한다. 원심분리기에서 탈수시킨 다음 건조 하면 평균입경이 10내지 100미크론의 폴리락산으로 캡슐화된 디클로르보스 80% 분말제제 1,000g을 얻었다.Into a reactor equipped with a high speed stirrer and a reflux cooler, dichlorobos 800g, acetone 200g, and polylactic acid 200g are heated, and refluxed and slowly stirred to dissolve. When all are dissolved, slowly add the aqueous solution of 100g of Monopol and 50g of NK-DIS20 in 3,000g of water to the solution and increase the stirring speed to maintain 3,000 revolutions per minute for 6 hours. When dehydrated in a centrifuge and dried to obtain 1,000 g of dichlorbos 80% powder formulation encapsulated with polylactic acid having an average particle diameter of 10 to 100 microns.

본 발명은 캡슐화된 살충제 약제 성분이 지속적으로 서서히 방출되므로 살충제의 살포 횟수 및 살포량을 줄이게 되어 약제살포로 인한 자연환경 오염과 약제살포에 따른 노력과 비용을 절약할 수 있는 효과가 있다.According to the present invention, the encapsulated insecticide drug ingredient is continuously released slowly, thereby reducing the spraying frequency and the spraying amount of the insecticide, thereby reducing the effort and cost according to the natural environmental pollution and the drug spraying due to the drug spraying.

Claims (3)

활성성분으로 유기인계 살충제 또는 피레스로이드계 살충제, 유기용제, 캡슐화제로서 폴리락산 및 계면활성제, 분산제, 점도조절제, 물에서 선택된 1종 이상의 보조제를 포함하는 생분해성 마이크로캡슐화 살충제.A biodegradable microencapsulated insecticide comprising an organophosphorus insecticide or a pyrethroid insecticide, an organic solvent and an encapsulating agent as an active ingredient, and polylactic acid and at least one auxiliary agent selected from surfactants, dispersants, viscosity modifiers and water. 제 1항에 있어서, 유기인계 살충제로서 클로로피리포스, 다이아지논, 훼니트로치온 또는 디클로로보스를 5-60중량% 함유하거나 피레스로이드계 살충제로서 델타메쓰린, 싸이퍼메쓰린 또는 퍼메쓰린을 1-30중량% 함유하는 것을 특징으로 하는 생분해성 마이크로캡슐화 살충제.The method according to claim 1, wherein the organophosphorus insecticide contains 5-60% by weight of chloropyriphos, diazinone, phenytrothion or dichloroboss, or deltamethrin, ciphermethrin or permethrin as pyrethroid insecticide. Biodegradable microencapsulated insecticide, characterized in that containing 30% by weight. 제 1항에 있어서, 살충제 조성물의 각 성분을 혼합, 교반하여 제조된 현탁액상, 또는 이 현탁액을 탈수, 건조하여 제조된 분말상인 것을 특징으로 하는 생분해성 마이크로캡슐화 살충제.The biodegradable microencapsulated insecticide according to claim 1, which is in the form of a suspension prepared by mixing and stirring the components of the insecticide composition, or a powder prepared by dehydrating and drying the suspension.
KR1019980046456A 1998-10-30 1998-10-30 Microcapsule insecticide using biodegradable polymeric material KR20000028283A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100457251B1 (en) * 2002-03-27 2004-11-16 주식회사 한국아핀사 microcapsule type insecticide and preparation process thereof
KR101016388B1 (en) * 2001-09-06 2011-02-21 신젠타 리미티드 Novel compounds
KR20150025995A (en) * 2013-08-30 2015-03-11 (주)국보싸이언스 urethane-urea composite microcapsule type insecticide

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101016388B1 (en) * 2001-09-06 2011-02-21 신젠타 리미티드 Novel compounds
KR100457251B1 (en) * 2002-03-27 2004-11-16 주식회사 한국아핀사 microcapsule type insecticide and preparation process thereof
KR20150025995A (en) * 2013-08-30 2015-03-11 (주)국보싸이언스 urethane-urea composite microcapsule type insecticide

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