KR100523798B1 - Mixed granular agent for an agriculture - Google Patents

Mixed granular agent for an agriculture Download PDF

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KR100523798B1
KR100523798B1 KR10-1999-0030572A KR19990030572A KR100523798B1 KR 100523798 B1 KR100523798 B1 KR 100523798B1 KR 19990030572 A KR19990030572 A KR 19990030572A KR 100523798 B1 KR100523798 B1 KR 100523798B1
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parts
active ingredient
pesticide active
probenazole
inner core
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KR10-1999-0030572A
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Korean (ko)
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KR20000012005A (en
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아라이마리코
오다와라겐지
오치아이가즈코
우오모토가츠히토
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오츠카 가가쿠 홀딩스 가부시키가이샤
메이지 세이카 가부시키가이샤
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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
    • 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
    • A01N25/08Biocides, 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 solids as carriers or diluents
    • 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
    • A01N31/00Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
    • A01N31/08Oxygen or sulfur directly attached to an aromatic ring system
    • A01N31/16Oxygen or sulfur directly attached to an aromatic ring system with two or more oxygen or sulfur atoms directly attached to the same aromatic ring system
    • 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
    • A01N43/48Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/561,2-Diazoles; Hydrogenated 1,2-diazoles
    • 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
    • A01N43/72Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/80Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
    • 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
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/24Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues 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
    • A01N51/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Dentistry (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Toxicology (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

본 발명은 제 1 농약 활성 성분과 제 2 농약 활성 성분을 함유하는 혼합 입제(粒劑)에 관한 것으로, 제 1 농약 활성 성분의 급격한 용출(溶出)을 방지하면서, 시용(施用) 직후부터 제 2 농약 활성 성분의 효과를 발현시킬 수 있는 농약용 혼합 입제를 얻는 것을 그 목적으로 한다.TECHNICAL FIELD The present invention relates to a mixed granule containing a first pesticide active ingredient and a second pesticide active ingredient, wherein the second pesticide is immediately after application while preventing rapid elution of the first pesticide active ingredient. It is an object of the present invention to obtain a mixed granule for agrochemicals capable of expressing the effect of an agrochemical active ingredient.

본 발명은 내핵 입자의 표면을 수지로 피복하고, 그 둘레에 외층부를 형성한 구조를 가지며, 제 1 농약 활성 성분이 주로 내핵 입자에 함유되어 있고, 제 2 농약 활성 성분이 주로 외층부에 함유되어 있는 것을 특징으로 하고 있다. The present invention has a structure in which the surface of the inner core particles is coated with a resin, and the outer layer portion is formed around the first core pesticide active ingredient mainly contained in the inner core particles, and the second pesticide active ingredient mainly contained in the outer layer part. It is characterized by that.

Description

농업용 혼합 입제{Mixed granular agent for an agriculture}Mixed granular agent for an agriculture}

본 발명은 혼합하여도 안정되게 사용할 수 있는 적어도 2종 이상의 농약 활성 성분을 함유하는 농업용 혼합 입제(粒劑)에 관한 것으로, 보다 상세하게는 각각의 농약 활성 성분의 효과 발현 시기를 제어할 수 있고, 약해(藥害) 발생의 우려가 적은 농업용 혼합 입제에 관한 것이다.The present invention relates to an agricultural mixed granule containing at least two or more pesticide active ingredients that can be stably used even when mixed. More specifically, the timing of effect expression of each pesticide active ingredient can be controlled. The present invention relates to agriculturally mixed granules, which are less likely to cause weakening.

최근, 농작업의 에너지 절약을 목적으로 하여, 각종 혼합제가 제안되고 있다. 이와 같은 혼합제로서는, 예를 들면, 살균 활성을 갖는 화합물과 살충 활성을 갖는 화합물을 동일제(同一劑)내에 배합한 살충 살균제가 알려져 있다.In recent years, various mixing agents have been proposed for the purpose of energy saving of agricultural work. As such a mixing agent, the insecticide fungicide which mix | blended the compound which has bactericidal activity, and the compound which has pesticidal activity in the same agent is known, for example.

그 중에서도, 살균 활성을 갖는 화합물로서 프로베나졸(Probenazole)을 이용하고, 살충 활성을 갖는 화합물로서 벤푸라카르브(Benfuracarb)를 이용한 혼합제는, 화합물 상호간에 분해 촉진 등의 악영향을 미치지 않고, 벼농사의 각종 병충해 방제에 매우 큰 효과를 갖고 있어 널리 이용되고 있다. 다만, 프로베나졸의 함유량이 충분히 많지 않은 경우, 지역에 따라서는 효과의 지속성이 충분하지 않은 경우가 있었다. 이 때문에, 프로베나졸 살균 효과의 지속성이 높은 혼합제가 요구되어, 프로베나졸의 함량을 늘리는 것이 고려되었다. 그러나 프로베나졸의 함유량을 늘리는 것은, 프로베나졸의 초기 용출(溶出)을 높여 약해 발생의 원인이 될 우려가 있었다.Among them, a mixing agent using Probenazole as a compound having bactericidal activity and Benfuracarb as a compound having insecticidal activity has no adverse effect such as promoting degradation among the compounds, It has a very large effect on the control of various pests and is widely used. However, when the content of probenazole is not high enough, the effect persistence may not be sufficient in some regions. For this reason, the admixture with high sustainability of the provenazole sterilization effect is calculated | required, and it was considered to increase the content of probenazole. However, increasing the content of probenazole could increase the initial elution of probenazole and cause weakening.

그런데, 이들 혼합제는, 산포(散布)시의 에너지 절약과 안전성의 면에서, 일반적으로 입제(粒劑) 형태로 사용되고 있다. 입제로서 일반적인 형태는, 농약 활성 성분과 점토같은 담체(擔體) 등을 혼합하고, 여기에 통상 물을 가하여 혼합하고 압출하여 조립(造粒)한 후, 건조하여 제조되는 압출형 입제이다. 이와 같은 입제 형태에서 프로베나졸의 함유량을 늘리면, 상술한 바와 같이 초기 용출 농도가 높아져, 살균 효과의 지속성을 충분히 높일 수 없었다. 또한, 다른 입제의 형태로서, 흡유성(吸油性)이 없는 입상 담체의 표면에 접착제를 이용하여 농약 활성 성분을 부착시켜 피복한 입제가 알려져 있다. 예를 들면, 일본국 특허공개 공보 평7-149606호에는, 접착제로서 수중에 유탁(乳濁)한 상태에 있는 수불용성 열가소성 수지를 이용하여, 비흡유성 입상 담체에 농약 활성 성분을 부착시켜 피복한 입제가 개시되어 있다. 이와 같은 방법으로 프로베나졸의 함유량을 높여 혼합 입제를 조제한 경우에도, 마찬가지로 프로베나졸의 초기 용출 농도가 높아져, 원하는 살균 효과의 지속성을 얻을 수 없었다.By the way, these mixing agents are generally used in granular form from the viewpoint of energy saving and safety at the time of dispersion. A general form of granules is an extruded granule which is prepared by mixing an active pesticide active ingredient with a carrier such as clay, mixing with water, extruding, granulating, and then drying. Increasing the content of probenazole in such a granulated form increased the initial elution concentration as described above, so that the sustainability of the bactericidal effect could not be sufficiently increased. In addition, granules coated with an agrochemical active ingredient with an adhesive on a surface of a particulate carrier having no oil absorption are known as other granules. For example, Japanese Patent Application Laid-open No. Hei 7-149606 uses a water-insoluble thermoplastic resin suspended in water as an adhesive to adhere a pesticide active ingredient to a non-oil-absorbing particulate carrier. Granulation is disclosed. Even in the case where a mixed granule was prepared by increasing the content of probenazole in such a manner, the initial elution concentration of probenazole was similarly high, and the desired sustainability of the bactericidal effect could not be obtained.

농약제제의 효과를 장시간 지속시키는 방법으로서, 농약제제에 서방성(徐放性)을 부여하는 방법이 알려져 있다. 농약제제에 서방성을 부여하는 방법으로는, 예를 들면, 농약 활성 성분과 담체 등을 혼합할 때에, 각종 폴리머, 왁스, 비정질 실리카 등의 농약 활성 성분의 용출을 방해하는 성분을 배합하여 용출 속도를 제어하는 방법, 서방성을 갖는 담체에 농약 활성 성분을 함침시키는 방법, 입제 표면에 수지 피막을 형성하여 용출 속도를 제어하는 방법 등이 알려져 있다.As a method of sustaining the effect of pesticide preparation for a long time, a method of imparting sustained release to pesticide preparations is known. As a method of imparting sustained release to a pesticide preparation, for example, when mixing a pesticide active ingredient and a carrier, a dissolution rate by formulating a component that prevents the dissolution of the pesticide active ingredient such as various polymers, waxes, amorphous silica, etc. The method of controlling the method, the method of impregnating a pesticide active ingredient in the carrier which has sustained release property, the method of forming a resin film on the granule surface, and controlling the elution rate are known.

하지만, 이들 방법을 상기 벤푸라카르브/프로베나졸 혼합제에 적용하면, 프로베나졸에 대해 충분한 서방성을 부여한 제형(劑型)에서는 벤푸라카르브의 살충 효과가 빠르게 발현되지 않는다는 문제를 일으키고, 한편 벤푸라카르브의 효과가 빠르게 발현하는 제형에서는 프로베나졸에 대한 서방성이 불충분해져, 약해 발생의 위험을 불식할 수 없다는 문제를 일으킨다.However, when these methods are applied to the benfuracarb / provenazole mixture, it causes a problem that the insecticidal effect of benfuracarb is not rapidly expressed in the formulations that give sufficient sustained release to provenazole, On the other hand, in the formulation in which the effect of benfuracarb is rapidly expressed, the sustained release to provenazole is insufficient, causing a problem that the risk of weakening cannot be eliminated.

또, 이와 같은 문제는 다른 농약 활성 성분의 조합에서도 발생하는 문제였다.Moreover, such a problem was also a problem which arises in the combination of another pesticide active ingredient.

본 발명의 목적은 제 1 농약 활성 성분과 제 2 농약 활성 성분을 함유하는 혼합 입제로서, 제 1 농약 활성 성분의 급격한 용출을 막으면서, 시용 직후부터 제 2 농약 활성 성분의 효과를 발현할 수 있는 농업용 혼합 입제를 제공하는데 있다.An object of the present invention is a mixed granule containing the first pesticide active ingredient and the second pesticide active ingredient, which can express the effect of the second pesticide active ingredient immediately after application while preventing the rapid dissolution of the first pesticide active ingredient. It is to provide an agricultural mixed granules.

본 발명의 농업용 혼합 입제는, 혼합하여도 안정되게 사용할 수 있는 제 1 농약 활성 성분과 제 2 농약 활성 성분을 함유하는 농업용 혼합 입제로서, 내핵 입자의 표면을 에멀젼 수지로 피복하고, 그 둘레에 외층부를 형성한 구조를 가지며, 제 1 농약 활성 성분이 주로 내핵 입자에 함유되어 있고, 제 2 농약 활성 성분이 주로 외층부에 함유되어 있으며, 제 1 농약 활성 성분이 프로베나졸(Probenazole)이고, 제 2 농약 활성 성분이 벤푸라카르브(Benfuracarb), 피프로닐(Fipronil), 에토펜프록스(Ethofenprox), 푸라티오카르브(Furathiocarb), 카르보술판(Carbosulfan) 및 이미다크로프리드(Imidacloprid)로 이루어진 군에서 선택되는 적어도 한 종임을 특징으로 하고 있다.The agricultural mixed granules of the present invention are agricultural mixed granules containing a first pesticide active ingredient and a second pesticide active ingredient that can be stably used even when mixed. The surface of the inner core particles is coated with an emulsion resin, and the outer layer is surrounded by an outer layer. It has a structure of forming a part, the first pesticide active ingredient is mainly contained in the inner core particles, the second pesticide active ingredient is mainly contained in the outer layer portion, the first pesticide active ingredient is Probenazole, 2 Pesticide active ingredients are Benfuracarb, Fipronil, Ethofenprox, Furathiocarb, Carbosulfan and Imidacloprid. At least one species selected from the group consisting of:

본 발명의 농업용 혼합 입제는, 높은 서방 효과의 부여가 요구되는 농약 활성 성분을 제 1 농약 활성 성분으로 하고, 빠른 효과의 발현이 요구되는 농약 활성 성분을 제 2 농약 활성 성분으로 하는 각종 농약 활성 성분의 조합에서 바람직하게 적용할 수 있다. 또한 본 발명의 농업용 혼합 입제에 이용되는 농약 활성 성분의 조합은, 혼합하여도 안정되게 사용할 수 있는 농약 활성 성분의 조합에 대해 바람직하게 적용된다. 즉, 농약 활성 성분의 화합물 상호간에 분해 촉진 등의 악영향이 없는 관계, 이른바 배합 금기가 아닌 관계에 있는 농약 활성 성분의 조합에 대해 바람직하게 적용된다.The mixed granules for agricultural use of the present invention are a pesticide active ingredient requiring a high sustained-release effect as a first pesticide active ingredient, and a pesticide active ingredient requiring rapid expression as a second pesticide active ingredient. It is preferably applicable in the combination of. Moreover, the combination of the pesticide active ingredient used for the agricultural mixed granulation of this invention is applied suitably with respect to the combination of the pesticide active ingredient which can be used stably even if it mixes. That is, the compound is preferably applied to a combination of pesticide active ingredients in a relationship that does not have adverse effects such as promoting degradation among the compounds of the pesticide active ingredient, and is not a so-called contraindication.

본 발명의 농업용 혼합 입제에 이용되는 농약 활성 성분으로서는, 살충 활성 성분, 살균 활성 성분, 제초(除草) 활성 성분 및 식물 성장 활성 성분 등을 예시할 수 있다. Examples of the pesticide active ingredient used in the agricultural mixed granules of the present invention include insecticidal active ingredients, bactericidal active ingredients, herbicide active ingredients, plant growth active ingredients and the like.

살충 활성 성분으로서는, 아세페이트(Acephate), 이소크사티온(Isoxathion), 이미다크로프리드(Imidacloprid), 에틸티오메톤(Ethylthiodemeton), 에토펜프록스(Ethofenprox), 카르탑(Cartap), 카르보술판(Carbosulfan), 크로펜테진(Clofentezine), 클로르피리포스메틸(Chlorpyrifas-methyl), 산화펜부타주석(Fenbutatin-oxide), 시클로프로트린(Cycloprothrin), 디메틸빈포스(Dimetylrinphos), 디메토에이트(Dimethoate), 시라프르오펜(Silafluofen), 다이아지논(Diazinon), 티오디카르브(Thiodicarb), 티오시크람(Thiocyclam), 테부페노지드(Tebufenozide), 니텐피람(Nitenpyram), 바미도티온(Vamidothion), 비펜트린(Bifenthrin), 피리다펜티온(Pyridaphenthion), 피리다벤(Pyridaben), 피리미포스메틸(Pyrimiphos-methyl), 피프로닐(Fipronil), 페니소브로모레이트(Phenisobromolate), 부프로페진(Buprofezin), 푸라티오카르브(Furathiocarb), 프로파포스(Propafos), 벤술탑(Bensultap), 벤푸라카르브, 폴모티온(Formothion), 마라톤(Malathon), 모노크로토포스(Monocrotophos), BPMC, CVMC, DEP, EPN, MEP, MIPC, MPP, MTMC, NAC, PAP, PHC, PMP, XMC 등을 들 수 있다. As insecticidal active ingredients, Acephate, Isoxathion, Imidacloprid, Ethylthiodemeton, Ethofenprox, Cartap, Carbosulphan (Carbosulfan), Crofentezine (Clofentezine), Chlorpyrifas-methyl, Fenbutatin-oxide, Cycloloprothrin, Dimetylrinphos, Dimethoate ), Silafluofen, Diazinon, Thiodicarb, Thiocyclam, Tebufenozide, Nitenpyram, Vamidothion, Bifenthrin, Pyridaphenthion, Pyridaben, Pyrimiphos-methyl, Fipronil, Phenisobromolate, Bupropezin (Buprofezin), Furathiocarb, Propafos, Bensultop ultap, Benfuracarb, Formothion, Marathon, Monocrotophos, BPMC, CVMC, DEP, EPN, MEP, MIPC, MPP, MTMC, NAC, PAP, PHC, PMP , XMC, and the like.

살균 활성 성분으로서는, 아시벤조랄(Acibenzolar)-S-메틸, 아족시스트로빈(Azoxystrobin), 이소푸로티올란(Isoprothiolane), 이소푸로디온(Isoprodion), 이미노크타딘초산염(Iminoctadine triacetate), 옥소리닉산(Oxolinic acid), 옥시퀴놀린구리(Oxone-copper), 카수가마이신(Kasugamycin), 카르프로파미드(Carpropamid), 캡탄(Captan), (RS)-2-시아노(cyano)-N-((R)-1-(2,4-디클로로페닐)에틸)-3,3-디메틸부틸아미드(개발상품번호 S-2900), 디클로메진(Diclomezine), 티아벤다졸(Thiabendazole), 티프루자미드(Thifluzamide), 테클로프타람(Tecloftalam), 트리시클라졸(Tricyclazole), 바리다마이신(Validamycin), 히드록시이소퀴사졸(Hydroxyisoxazole), 피로퀴론(Pyroquilon), 페나리몰(Fenarimol), 페림존(Ferimzone), 푸사라이드(Fthalide), 블라스트사이딘(Blasticidin), 푸라메트필(Furametpyr), 프루트라닐(Flutlanil), 프로베나졸, 펜시쿠론(Pencycuron), 폴리옥신(Polyoxin), 메타술포카르브(Methasulfocarb), 메타락실(Metalaxl), 메타락실-M, 메토미노스트로빈(Metominostrobin), 메프로닐(Mepronil), CNA, IBP, DF-351, NNF-9425, NNF-9850, (RS)-2-(4-플루오로페닐)-1-(1H-1,2,4-트리아졸-1-일(il))-3-트리메틸시릴프로판-2-올(SF·9701) 등을 들 수 있다.As bactericidal active ingredients, Acibenzolar-S-methyl, Azoxystrobin, Isoprothiolane, Isoprorodion, Iminoctadine triacetate, Oxolinic acid acid), Oxyquinolin copper (Oxone-copper), Kasugamycin, Carpropamid, Captan, (RS) -2-cyano-N-((R) -1- (2,4-dichlorophenyl) ethyl) -3,3-dimethylbutylamide (Development Product No. S-2900), Diclomezine, Thiabendazole, Thifluzamide , Tecloftalam, Tricyclazole, Varidamycin, Hydroxyisoxazole, Pyroquilon, Penarimol, Ferrimzone, Ferrimzone, Fthalide, Blasticidin, Furammetpyr, Flutlanil, Provenazole, Pencycuron, Polyox (Polyoxin), Metasulfocarb, Metalaxyl, Metalaxyl, Metalaxyl-M, Metominostrobin, Mepronil, CNA, IBP, DF-351, NNF-9425, NNF-9850, (RS) -2- (4-fluorophenyl) -1- (1H-1,2,4-triazol-1-yl (il))-3-trimethylsilylpropan-2-ol ( SF9701) and the like.

제초 활성 성분 및 식물 성장 조절 성분으로서는, 아짐술푸론(Azimsulfuron), 아트라진(Atrazine), 아메트린(Ametryn), 이나벤피드(Inabenfide), 이마조술푸론(Imazosulfuron), 우니코나졸(Nuiconazole), 에스프로카르브(Esprocarb), 에토벤자니드(Etobenzanid), 옥사디아존(Oxadiazon), 카펜스트롤(Cafenstrole), 퀴자로폽에틸(Quizalofop-ethyl), 퀸크롤락(Quinclorac), 쿠밀론(Cumylron), 클로메톡시닐(Chlomethoxynil), 시클로술파무론(Cyclosulfamuron), 디티오필(Dithiopyr), 시노술푸론(Cinosulfuron), 시하로폽부틸(Cyhalofop-butyl), 시마진(Simazine), 디메타메트린(Dimetametryn), 디메피페레이트(Dimepiperate), 신메스린(Cinmethylin), 다임론(Dymron), 테닐크롤(Thenylchor), 트리아펜테놀(Triapenthenol), 나프로아니리드(Naproanilide), 파크로부트라졸(Paclobutrazol), 비페녹스(Bifenox), 피페로포스(Piperophos), 피라족시펜(Pyrazoxyfen), 피라조술푸론에틸(Pyrazosulfuron-ethyl), 피라조레이트(Pyrazolate), 피리부티카르브(Pyributicarb), 피리미노백메틸(Pyriminobac-methyl), 부타크롤(Butachlor), 부타미포스(Butamifos), 프레티라크롤(Pretilachlor), 브로모부티드(Bromobutide), 벤술푸론메틸(Bensulfuron-methyl), 벤조페납(Benzofenap), 벤타존(Bentazon), 벤티카르브(Benthiocarb), 펜토크사존(Pentoxazone), 벤푸레세이트(Benfuresate), 메페나셋트(Mefenacet), 몰네이트(Molinate), ACN, CNP, 2,4-D, MCPB, MCPB 에틸 등 및 식물 성장 조절제 등을 들 수 있다.Herbicidal active ingredients and plant growth regulators include Azimsulfuron, Atrazine, Ametryn, Inabenfide, Imazosulfuron, Uniconazole, S. Esprocarb, Etobenzanid, Oxadiazon, Carfenstrole, Quizarofop-ethyl, Quinclorac, Cumylron , Chlomethoxynil, Cyclosulfamuron, Dithiopyr, Cinosulfuron, Cyhalofop-butyl, Simazine, Dimethamethine ( Dimetametryn, Dimepiperate, Cinmethylin, Dymron, Thenylchor, Triaphentenol, Naproanilide, Paclobutrazol ), Bifenox, Piperophos, Pyrazoxyfen, Pyrazulfuronethyl (Py) razosulfuron-ethyl, Pyrazolate, Pyributicarb, Pyriminobac-methyl, Butachlor, Butamifos, Pretilachlor, Bromobutide, Bensulfuron-methyl, Benzofenap, Bentazon, Benthiocarb, Pentoxazone, Benfuresate, Menfuresate Mefenacet, molinate, ACN, CNP, 2,4-D, MCPB, MCPB ethyl and the like, and plant growth regulators.

일반적으로 농약 활성 성분 중에는, 한 시기에 대량으로 용출함으로써, 작물에 해를 입히거나, 어류 등의 수생(水生) 생물에 영향을 주거나, 혹은 악취가 강해지는 등의 문제를 발생시키는 것도 존재한다. 통상, 농약 활성 성분의 용출량을 제어함으로써 그 문제들을 회피할 수 있다. 또한, 용출량을 제어함으로써 효과의 지속성을 부여하는 것도 기대할 수 있다. 본 발명에 따른 바람직한 혼합제의 한 실시 형태에서는, 서로 다른 활성 성분 중에서, 어떠한 목적에 따라 용출량의 제어가 더욱 필요한 활성 성분을 제 1 농약 활성 성분으로 하고, 다른쪽 활성 성분을 제 2 농약 활성 성분으로 하여 적용하는 것이 바람직하다. 이와 같은, 농약 활성 성분의 조합으로서는, 구체적으로, 제 1 농약 활성 성분으로서의 프로베나졸 및 제 2 농약 활성 성분으로서의 벤푸라카르브, 피프로닐, 에토펜프록스, 푸라티오카르브, 카르보술판, 이미다크로프리드에서 선택되는 적어도 한 종의 조합을 들 수 있다. 특히, 대표적인 예로서는, 제 1 농약 활성 성분으로서 프로베나졸을 이용하고, 제 2 농약 활성 성분으로서 벤푸라카르브를 이용한 입제를 들 수 있다.Generally, some of the pesticide active ingredients are eluted in large quantities at one time, causing problems such as damage to crops, affecting aquatic organisms such as fish, or strong odor. Usually, the problems can be avoided by controlling the elution amount of the pesticide active ingredient. Moreover, it can also be expected to provide the persistence of the effect by controlling the amount of elution. In one embodiment of the preferred admixture according to the present invention, among the different active ingredients, the active ingredient which further needs to be controlled for elution according to a certain purpose is used as the first pesticide active ingredient, and the other active ingredient is used as the second pesticide active ingredient. It is preferable to apply. As such a combination of pesticide active ingredients, specifically, benvencarcarb, fipronil, etofenprox, furathiocarb, and carbosulfane as the first pesticide active ingredient and provenazole as the second pesticide active ingredient And combinations of at least one species selected from imidacroprids. In particular, examples thereof include granules using provenazole as the first pesticide active ingredient and benfuracarb as the second pesticide active ingredient.

제 1 농약 활성 성분으로서 바람직하게 이용되는 프로베나졸은, 일반명 3-아릴옥시-1,2-벤조이소티아졸-1,1-디옥시드이며, 도열병의 방제에 탁월한 효과를 갖는 화합물이다. 본 발명의 입제에 있어서의 프로베나졸의 배합량은, 입제 전체에 대해 3∼70중량%가 바람직하고, 더욱 바람직하게는 8∼70중량%, 더욱 바람직하게는 8∼50중량%이다.Probenazole, which is preferably used as the first pesticide active ingredient, is a generic name 3-aryloxy-1,2-benzoisothiazole-1,1-dioxide, and is a compound having an excellent effect in controlling the blasting disease. As for the compounding quantity of the provenazole in the granule of this invention, 3 to 70 weight% is preferable with respect to the whole granule, More preferably, it is 8 to 70 weight%, More preferably, it is 8 to 50 weight%.

제 2 농약 활성 성분으로서 바람직하게 이용되는 벤푸라카르브는, 화학명 에틸=N-[2,3-디히드로-2,2-디메틸벤조푸란-7-이르옥시카르보닐(메틸)아미노티오]-N-이소프로필-β-아라니나아트(alaninate)이고, 벼뿌리바구미(Lissorhoptrus oryzophilus), 애멸구(Laodelphax striatellus), 흰등멸구(Sogatella furcifera), 풀멸구(Nephotettix cincticeps), 벼잎벌레(Oulema oryzae), 아페렌추이데스 베세이(Aphelenchoides besseyi) 등의 해충 방제에 높은 효과를 갖는다. 본 발명의 입제에 있어서 벤푸라카르브의 배합량은, 입제 전체에 대해 바람직하게는 1∼30중량%, 더욱 바람직하게는 1∼20중량%이다.Benfuracarb which is preferably used as the second pesticide active ingredient, has the chemical name ethyl = N- [2,3-dihydro-2,2-dimethylbenzofuran-7-iroxycarbonyl (methyl) aminothio]- N-isopropyl-β-alaninate, Lisorhoptrus oryzophilus, Laodelphax striatellus, Sogatella furcifera, Nephotettix cincticeps, Olema oryzae It is highly effective in controlling pests such as Aphelenchoides besseyi. In the granulation of the present invention, the blending amount of benfuracarb is preferably 1 to 30% by weight, more preferably 1 to 20% by weight based on the entire granulation.

본 발명에서, 제 1 농약 활성 성분 및 제 2 농약 활성 성분으로서 그 밖의 농약 활성 성분을 이용하는 경우에는, 상기 배합량을 기준으로, 농약 활성 성분의 약효를 고려하여 적절히 배합량을 조정할 수 있다.In the present invention, in the case of using other pesticide active ingredients as the first pesticide active ingredient and the second pesticide active ingredient, the compounding amount can be appropriately adjusted in consideration of the medicinal effects of the pesticide active ingredient based on the above compounding amount.

본 발명에 따른 입제의 내핵 입자는, 제 1 농약 활성 성분, 고체 담체 및 필요에 따라 배합되는 그 밖의 성분으로 구성된다.The inner core particles of the granules according to the present invention are composed of the first pesticide active ingredient, a solid carrier and other ingredients to be blended as necessary.

고체 담체로서는, 벤토나이트(bentonite), 점토(clay), 고령토(kaolin), 견운모(sericite), 활석(talc), 산성 백토(白土), 경석(輕石), 불석(zeolite), 질석(vermiculite), 진주암(pearlite), 탄산칼슘, 규사 등을 예시할 수 있다. Examples of the solid carrier include bentonite, clay, kaolin, sericite, talc, acidic clay, pumice, zeolite and vermiculite. , Pearlite, calcium carbonate, silica sand and the like can be exemplified.

또, 그 밖의 성분으로서는, 왁스 등의 서방성 향상제, 알킬황산에스테르염류, 아릴술폰산염류, 폴리옥시에틸렌글리코올에테르류, 다가알코올에스테르류, 디알킬술포삭시네이트류, 폴리카르본산류 등의 계면 활성제, 전분, 알긴산, 글리세린, 폴리비닐피롤리돈, 폴리우레탄, 폴리에틸렌글리코올, 폴리프로필렌글리코올, 폴리부텐, 폴리비닐알코올, 아라비아고무, 유동파라핀, 에틸셀룰로우즈, 폴리비닐아세테이트 등의 결합제, 염료, 안료 등의 착색제 등을 예시할 수 있다.Moreover, as other components, such as sustained release improvers, such as a wax, alkyl sulfate ester salts, aryl sulfonate, polyoxyethylene glycol ethers, polyhydric alcohol esters, dialkyl sulfosuccinates, polycarboxylic acids, etc. Surfactant, starch, alginic acid, glycerin, polyvinylpyrrolidone, polyurethane, polyethylene glycol, polypropylene glycol, polybutene, polyvinyl alcohol, gum arabic, liquid paraffin, ethyl cellulose, polyvinylacetate Coloring agents, such as a binder, dye, and a pigment, etc. can be illustrated.

본 발명의 입제 내핵 입자에는 수지로 이루어지는 피막이 형성된다. 수지로서는 에멀전 수지가 바람직하고, 상기 에멀전 수지로서는, 폴리우레탄수지, 초산비닐수지, 스틸렌수지, 아크릴수지와 이들의 공중합체, 및 이들 혼합물의 에멀전을 예시할 수 있다. 제조시 에멀전의 고형분 함량은, 특히 제한은 없지만, 1∼55중량%가 바람직하고, 더욱 바람직하게는 15∼45중량%이다.The granular inner core particles of the present invention are formed with a resin film. As resin, an emulsion resin is preferable, and as said emulsion resin, the emulsion of a polyurethane resin, a vinyl acetate resin, a styrene resin, an acrylic resin, a copolymer thereof, and these mixture can be illustrated. Although there is no restriction | limiting in particular in solid content of emulsion at the time of manufacture, 1-55 weight% is preferable, More preferably, it is 15-45 weight%.

폴리우레탄수지의 시판품으로서는, 예를 들면 상품명 「닛포란 2606」(니폰폴리우레탄고교 가부시키가이샤), 상품명 「본딕 2220」, 「하이드란 AP-20」, 「하이드란 AP-40(F)」(다이니폰잉키가가쿠고교 가부시키가이샤), 상품명 「파머린 UA-150」(산요가세이고교 가부시키가이샤), 상품명 「올레스타 UD100N」(미츠이가가쿠 가부시키가이샤), 상품명 「수퍼플렉스 160」, 「수퍼플렉스 750」, 「수퍼플렉스 410」, 「수퍼플렉스 126」(다이이치고교 세이야쿠 가부시키가이샤) 등을 들 수 있다.As a commercial item of a polyurethane resin, for example, a brand name "Nipporan 2606" (Nippon Polyurethane High School Co., Ltd.), a brand name "Bondick 2220", "Hylan AP-20", "Hylan AP-40 (F)" (Dai Nippon Ingiga Chemical Co., Ltd.), a brand name `` Parmaline UA-150 '' (Sanyo Sego Co., Ltd.), a brand name `` Olesta UD100N '' (Mitsuigagaku Kabuki Kaisha), a brand name `` Superplex 160 "," Superplex 750 "," Superplex 410 "," Superplex 126 "(Daiichigogyo Seiyaku Co., Ltd.), etc. are mentioned.

이들 수지에는 조막(造膜) 보조제로서 부틸셀로솔브, 칼비토올, 부틸칼비토올, 메틸셀로솔브, 부틸셀로솔브아세테이트, 칼비토올아세테이트, 부틸칼비토올아세테이트, 메틸셀로솔브아세테이트 등을 배합하여 이용할 수 있다. 배합량으로서는 고형분에 대해 통상 0∼15%, 많게는 50% 정도를 예시할 수 있다.These resins include butyl cellosolve, carbitol, butyl carbitol, methyl cellosolve, butyl cellosolve acetate, carbitolol acetate, butyl carbitol acetate, and methyl cellosolve as a film forming aid. Acetate etc. can be mix | blended and used. As a compounding quantity, 0 to 15% normally, about 50% can be illustrated with respect to solid content normally.

본 발명의 입제 외층부는 제 2 농약 활성 성분 및 필요에 따라 배합되는 그 밖의 성분으로 구성된다.The granular outer layer part of this invention is comprised from a 2nd pesticide active ingredient and the other component mix | blended as needed.

그 밖의 성분으로서는, 알칼리금속염, 알칼리토류금속염, 에폭시화유지류 등의 농약 활성 성분 안정제, 벤토나이트, 규조토, 화이트카본 등의 고체 담체 및 내핵 입자 성분으로서 예시한 고체 담체, 서방성 향상제, 계면 활성제, 결합제, 그 밖의 농약 활성 성분 등을 예시할 수 있다. Other components include agrochemical active ingredient stabilizers such as alkali metal salts, alkaline earth metal salts and epoxidized oils and fats, solid carriers such as bentonite, diatomaceous earth and white carbon, and solid carriers exemplified as inner core particle components, sustained release enhancers, surfactants, and binders. And other pesticide active ingredients.

본 발명의 입제에서는, 외층부에 파라핀왁스 등의 서방성 향상제를 배합하거나, 외층부의 더 외측에 에멀전 수지 등으로 이루어지는 피막을 형성함으로써, 제 1 농약 활성 성분 및 제 2 농약 활성 성분의 양자에 서방성을 부여한 입제로 하는 것도 가능하며, 그 입제에서는 제 1 농약 활성 성분의 서방화 효과가 제 2 농약 활성 성분의 서방화 효과보다도 상대적으로 높게 설정된 것이 된다.In the granulation of the present invention, a sustained release agent such as paraffin wax is blended into the outer layer portion, or a film made of an emulsion resin or the like is formed on the outer layer portion so that the first pesticide active ingredient and the second pesticide active ingredient are both released slowly. It is also possible to set the granule to which the property is imparted, in which the sustained release effect of the first pesticide active ingredient is set relatively higher than the sustained release effect of the second pesticide active ingredient.

본 발명의 입제 제조시에는, 1) 제 1 농약 활성 성분과 고체 담체, 필요에 따라 그 밖의 성분을, 압출 조립기(造粒機), 교반 조립기, 전동 조립기 혹은 유동층 조립기 등 통상의 혼합 조립기를 이용하여 제조하는 방법, 2) 제 1 농약 활성 성분을 함유하지 않고 상기 1)과 동일한 방법으로 얻은 중심 입자(芯粒)에 콘크리트믹서, 나우타믹서 등 통상의 혼합기를 이용하여, 제 1 농약 활성 성분을 함침(含浸)시키는 방법, 또는 3) 규사 및 탄산칼슘 등의 비흡유성 담체 표면에 제 1 농약 활성 성분을 필요에 따라 고체 담체나 그 밖의 성분과 함께, 적절한 바인더를 이용하여 부착시키는 방법 등에 의해 내핵 입자를 제조한다. 그 내핵 입자의 형상으로는, 직경이 0.1∼30㎜인 구형상물, 직경 0.1∼5㎜, 길이 1∼30㎜, 어스펙트비(길이/직경) 1∼10인 원통형상물 등을 예시할 수 있다.In the preparation of the granules of the present invention, 1) a conventional agrochemical granulator such as an extrusion granulator, a stirring granulator, a rolling granulator or a fluidized bed granulator is used as the first pesticide active ingredient, a solid carrier and, if necessary, other components. 2) The first pesticide active ingredient is prepared by using a conventional mixer, such as a concrete mixer or a Nauta mixer, to the central particles obtained by the same method as in 1) without containing the first pesticide active ingredient. Impregnation or 3) a method of adhering the first pesticide active ingredient to the surface of a non-oil-absorbing carrier such as silica sand and calcium carbonate with a solid carrier or other components, if necessary, using an appropriate binder, or the like. Prepare the particles. As the shape of the inner core particles, a spherical material having a diameter of 0.1 to 30 mm, a diameter of 0.1 to 5 mm, a length of 1 to 30 mm, and a cylindrical shape having an aspect ratio (length / diameter) of 1 to 10 can be exemplified. .

계속해서 에멀전 수지 등의 수지를, 분무 또는 적하(滴下) 등의 수단에 의해 내핵 입자 표면에 피복하여 건조시키거나, 혹은 미건조 상태에서 외층부의 구성 성분을 차례로 또는 동시에 첨가할 수 있다. 이 때, 상온이나, 혹은 가열하에서 첨가할 수 있고, 또 첨가후에 가열, 감압, 송풍 등의 수단을 이용하여 건조시킬 수 있다. 다만, 건조를 행하지 않거나, 일부 미건조로 하는 등의 수단에 의해 피막에 점착성 또는 접착성을 부여한 상태에서 외층부의 구성 성분을 첨가함으로써 외층부의 부착성 향상을 도모할 수도 있다. 이들 공정은, 콘크리트 믹서, 나우터 믹서(Knowter mixer), 리본 믹서 등 통상의 혼합기를 이용하여 내핵 입자를 혼합 혹은 전동(轉動)시키면서 행하는 것이 바람직하다.Subsequently, resin, such as an emulsion resin, is coat | covered and dried on the inner core particle surface by means of spraying or dripping, or the component of an outer layer part can be added one by one or simultaneously simultaneously in an undried state. At this time, it can be added at normal temperature or under heating, and after addition, it can be dried using means, such as heating, pressure reduction, and blowing. However, the adhesiveness of an outer layer part can also be improved by adding the structural component of an outer layer part in the state which provided adhesiveness or adhesiveness to a film by means, such as not drying or making it partially dry. It is preferable to perform these processes, mixing or driving inner core particle | grains using normal mixers, such as a concrete mixer, a Knoter mixer, and a ribbon mixer.

적용 작물의 예 : 논에 심은 벼(水稻)Example of Applied Crops: Rice Planted in Paddy Fields

사용 방법 : 육묘(育苗) 상자How to use: seedling box

10 아르(a)당 사용량 : 0.1∼10㎏, 통상 1㎏ 정도Usage amount per 10 ar (a): 0.1-10 kg, usually about 1 kg

사용 시기 : 모내기 전When to use: Before planting

(실시예)(Example)

이하, 실시예, 비교예 및 시험예를 들어 본 발명을 보다 상세히 설명한다. 또한, 이하, 단지 "부"로 표기한 것은 "중량부"를, "%"로 표기한 것은 "중량%"를 나타낸다.Hereinafter, the present invention will be described in more detail with reference to Examples, Comparative Examples and Test Examples. In addition, hereinafter, only "parts" means "parts by weight", and "%" indicates "% by weight".

실시예 1Example 1

프로베나졸 원체(technical product) 12부(유효성분량), 벤토나이트(상품명 「C벤토」, 네오라이트고산 가부시키가이샤) 3부, 알파화 전분(상품명 「마츠노린 M」, 마츠다니가가쿠 가부시키가이샤) 2부를 가하고, 점토(상품명 「NO 점토」, 네오라이트고산 가부시키가이샤)를 상기 성분과 합하여 80부가 되도록 더 가하여 혼합하고, 물 24부를 첨가하여 혼합한 후, 압출 조립기(바스켓 류저, 후지파우다루 가부시키가이샤)로 직경 1.2㎜인 원통형으로 압출하고, 사이징하여 어스펙트비 약 3으로 한 후, 60℃에서 2시간 건조하여, 내핵 입자 (A)를 얻었다.12 parts of probenazole technical substance (active ingredient amount), bentonite (brand name "C bento", neo-light high altitude Kabushi Kaisha), 3 parts of alpha starch (brand name "Matsunorin M", Matsutani Kagaku Kashiki) Kaisha) 2 parts were added, clay (brand name "NO clay", neo-light algae Co., Ltd.) was added to 80 parts of the above ingredients, mixed, and 24 parts of water were added and mixed, followed by extrusion granulator (basket riser, Fuji). The powder was extruded into a cylindrical shape having a diameter of 1.2 mm, powdered, and sized to an aspect ratio of about 3. Then, dried at 60 ° C. for 2 hours to obtain an inner core particle (A).

얻어진 내핵 입자 (A)를 콘크리트 믹서로 전동시키면서, 폴리우레탄 수분산체(상품명 「수퍼플렉스130」, 다이이치고교 세이야쿠 가부시키가이샤, 고형분 함량 35%) 4부를 내핵 입자 (A)의 표면에 스프레이함으로써, 표면에 폴리우레탄 피막을 형성하고, 화이트카본 0.3부를 첨가한 후 60℃에서 2시간 건조하였다. 얻어진 폴리우레탄 피복 내핵 입자를 교반하면서, 벤푸라카르브 원체 2.5부(유효성분량) 및 화이트카본(상품명 「톡시일AL-1」, 가부시키가이샤 도쿠야마) 1.5부를 여러 차례로 나누어 번갈아 첨가하고, 계속해서 점토(NO 점토)를 고형분으로 전체가 100부가 되도록 첨가하여, 실시예 1의 살충 살균 혼합 입제를 얻었다.While spraying the obtained inner core particles (A) with a concrete mixer, spray 4 parts of polyurethane water dispersion (brand name "Superflex 130", Daiichi-kyokyo Seiyaku Co., Ltd., 35% solids content) to the surface of the inner core particles (A). By forming a polyurethane film on the surface by adding 0.3 part of white carbon, it dried at 60 degreeC for 2 hours. While stirring the obtained polyurethane-coated inner core particles, 2.5 parts (the amount of active ingredient) of benfuracarb element and 1.5 parts of white carbon (brand name "Toxyyl AL-1", Tokuyama Co., Ltd.) were added several times alternately, and it continued. Thus, the clay (NO clay) was added so that the whole was 100 parts in solid content, and the insecticidal sterilization mixed granule of Example 1 was obtained.

실시예 2Example 2

프로베나졸 원체 24부(유효성분량), 벤토나이트(C벤트) 3부, 폴리비닐알코올(상품명 「PVA 224」, 클라레 가부시키가이샤) 2부를 가하고, 점토(NO 점토)를 상기 성분과 합하여 81.2부가 되도록 가하여 더 혼합하고, 물 23.3부를 첨가하여 혼합한 후, 바스켓 류저로 직경 1㎜, 어스펙트비 약 3인 원통형 내핵 입자를 얻고, 이를 60℃에서 2시간 건조하여 내핵 입자 (B)를 얻었다.24 parts of Probenazole original substance (active ingredient amount), 3 parts of bentonite (C vent), 2 parts of polyvinyl alcohol (trade name "PVA 224", Clare Kabushi Kaisha) were added, and the clay (NO clay) was added to the above ingredients. After addition, the mixture was further mixed, 23.3 parts of water was added and mixed, and cylindrical basket particles having a diameter of 1 mm and an aspect ratio of about 3 were obtained with a basket flowr, and dried at 60 ° C. for 2 hours to obtain an inner core particle (B). .

얻어진 내핵 입자 (B)를 콘크리트 믹서로 전동시키면서, 아이오노머(ionomer)형 수성 우레탄 수지(상품명 「하이드란 AP-20」, 다이니폰잉키가가쿠고교 가부시키가이샤, 고형분 30%) 7부를 내핵 입자 표면에 스프레이함으로써, 표면에 폴리우레탄 피막을 형성하고, 탄산칼슘 1.5부를 더 첨가하였다. 60℃에서 2시간 건조한 후, 얻어진 폴리우레탄 피복 내핵 입자를 교반하면서, 벤푸라카르브 원체 5부(유효성분량) 및 화이트카본(상품명 「카프렉스 #1120」, 시오노기 세이야쿠 가부시키가이샤) 3.5부를 여러 차례로 나누어 번갈아 첨가하고, 점토(NO 점토)를 고형분으로 전체가 100부가 되도록 첨가하여, 실시예 2의 살충 살균 혼합 입제를 얻었다.7 parts of ionomer type aqueous urethane resin (brand name "Hylan AP-20", Dainippon Ingiga Chemical Co., Ltd., 30% of solid content), while rolling the obtained inner core particle (B) with a concrete mixer. By spraying on the surface, a polyurethane film was formed on the surface, and 1.5 parts of calcium carbonate was further added. After drying at 60 ° C. for 2 hours, 5 parts of Benfuracarb element (active ingredient amount) and white carbon (trade name "Caprex # 1120", Shionogi Seiyaku Co., Ltd.) 3.5 while stirring the obtained polyurethane-coated inner core particles 3.5 The parts were divided in turn and added alternately, and the clay (NO clay) was added so that the whole was 100 parts in solid content, and the insecticidal sterilization mixed granule of Example 2 was obtained.

실시예 3Example 3

실시예 2와 동일하게 하여 얻어진 내핵 입자 (B)를 콘크리트 믹서로 전동시키면서, 폴리우레탄 수분산체(상품명 「수퍼플렉스126」, 다이이치고교 세이야쿠 가부시키가이샤, 고형분 함량 30%) 8부를 내핵 입자의 표면에 스프레이함으로써, 표면에 폴리우레탄 피막을 형성하고, 그 후 60℃에서 2시간 건조하였다. 얻어진 폴리우레탄 피막 내핵 입자를 교반하면서, 벤푸라카르브 원체 5부(유효성분량) 및 화이트카본(상품명 「카프렉스 CS-7」, 시오노기 세이야쿠 가부시키가이샤) 3부를 여러 차례로 나누어 번갈아 첨가하고, 계속해서 점토(NO 점토)를 고형분으로 전체가 100부가 되도록 첨가하여, 실시예 3의 살충 살균 혼합 입제를 얻었다.8 parts of polyurethane aqueous dispersions (brand name "Superflex 126", Daiichi-kyokyo Seiyaku Co., Ltd., 30% of solid content) while carrying out the inner core particle (B) obtained by carrying out similarly to Example 2 with a concrete mixer By spraying on the surface of, a polyurethane film was formed on the surface, and it dried at 60 degreeC after that for 2 hours. While stirring the obtained polyurethane-film inner core particles, 5 parts (the active ingredient amount) of benfuracarb and 3 parts of white carbon (brand name "Caprex CS-7" and Shionogi Seiyaku Co., Ltd.) are added several times alternately, Then, the clay (NO clay) was added so that the whole may be 100 parts with solid content, and the insecticidal sterilization mixed granulation of Example 3 was obtained.

실시예 4Example 4

프로베나졸 원체 24부(유효성분량), 벤푸라카르브 원체 2.5부(유효성분량), 벤토나이트(C벤토) 3부, 폴리비닐알코올(PVA 224) 2부를 가하고, 더욱이 점토(NO 점토)를 상기 성분과 합하여 78.4부가 되도록 가하여 혼합하고, 물 13.3부 및 특수 파라핀계왁스(상품명 「푸르닛 101Z」, 신나카무라가가쿠 가부시키가이샤 제품, 고형분 함량 50%) 10부를 첨가하여 혼합한 후, 바스켓 류저(스크린 1.0㎜)를 이용하여 원통형 내핵 입자를 얻고, 이를 마르메라이져를 이용하여 정립(整粒)하여 어스펙트비(긴지름/짧은지름)가 약 1.5인 거의 구형의 내핵 입자 (C)를 얻었다.24 parts of Probenazole original (active ingredient), 2.5 parts of Benfuracarb original (active ingredient amount), 3 parts of bentonite (C bento), and 2 parts of polyvinyl alcohol (PVA 224) were added, and the clay (NO clay) The mixture was added to 78.4 parts, mixed, and mixed with 13.3 parts of water and 10 parts of special paraffin wax (trade name "Purnet 101Z", manufactured by Shin-Nakamura Chemical Co., Ltd., 50% solids content), followed by a basket riser. Cylindrical inner core particles were obtained using (screen 1.0 mm), which were sized using a marmerizer to obtain almost spherical inner core particles (C) having an aspect ratio (long diameter / short diameter) of about 1.5. .

얻어진 내핵 입자 (C)를 콘크리트 믹서로 전동시키면서, 초산비닐계 수지 에멀전(상품명 「폴리조올 S-400」, 쇼와고분시 가부시키가이샤, 고형분 함량 53%) 4.5부를 내핵 입자의 표면에 스프레이 처리함으로써, 표면에 폴리우레탄 피막을 형성하고, 교반을 계속하면서 점토(NO 점토), 벤푸라카르브 원체 2.5부(유효성분량)를 서서히 첨가하고, 60℃에서 2시간 건조하여, 실시예 4의 살충 살균 혼합 입제 100부를 얻었다.4.5 parts of vinyl acetate-based resin emulsions (brand name "Polyzool S-400", Showa Kobunshi Co., Ltd., 53% of solid content) are spray-treated on the surface of an inner core particle, rolling the obtained inner core particle (C) with a concrete mixer. Thereby, a polyurethane film is formed on the surface, 2.5 parts (active ingredient amount) of clay (NO clay) and benfuracarb element are gradually added while continuing stirring, and dried at 60 degreeC for 2 hours, and the insecticide of Example 4 is carried out. 100 parts of sterile mixed granules were obtained.

실시예 5Example 5

실시예 3에서, 폴리우레탄 수분산액(수퍼플렉스 126) 8부를 대신하여, 락카형 폴리우레탄수지(상품명 「바아녹 16-411」, 다이니폰잉키가가쿠 가부시키가이샤 제품, 고형분 함량 50%) 5부를 이용하는 이외는, 모두 동일하게 하여, 실시예 5의 살충 살균 혼합 입제를 얻었다.In Example 3, in place of 8 parts of polyurethane aqueous dispersion (Superflex 126), lacquer-type polyurethane resin (trade name "Baan Nok 16-411", Dainippon Ingiga Chemical Co., Ltd., solid content 50%) 5 Except for using a part, it carried out similarly to all, and the insecticidal sterilization mixed granulation of Example 5 was obtained.

실시예 6Example 6

프로베나졸 원체 24부(유효성분량), 벤토나이트(C벤토) 3부, 폴리비닐알코올(상품명 「PVA 224」, 클라레 가부시키가이샤) 2부를 가하고, 점토(NO점토)를 상기 성분과 합하여 74.7부가 되도록 가하여 더 혼합하고, 물 23부를 첨가하여 혼합한 후, 바스켓 류저로 직경 1㎜, 어스펙트비 약 3의 원통형 내핵 입자를 얻고, 60℃에서 2시간 건조하여 내핵 입자 (D)를 얻었다.24 parts of Probenazole original (active ingredient amount), 3 parts of bentonite (C bento), 2 parts of polyvinyl alcohol (trade name "PVA 224", Clare Kabushi Kaisha) were added, and the clay (NO clay) was added to the above ingredients, and 74.7 After addition, the mixture was further mixed, 23 parts of water was added and mixed, and cylindrical basket particles having a diameter of 1 mm and an aspect ratio of about 3 were obtained with a basket flowr, and dried at 60 ° C. for 2 hours to obtain internal core particles (D).

얻어진 내핵 입자 (D)를 콘크리트믹서로 전동시키면서, 아이오노머형 수성 우레탄 수지(상품명 「하이드란 AP-40(F)」, 다이니폰잉키가가쿠고교 가부시키가이샤 제품, 고형분 22.5%) 6.5부를 내핵 입자 표면에 스프레이함으로써, 표면에 폴리우레탄 피막을 형성하고, 그 후 60℃에서 2시간 건조하였다. 얻어진 폴리우레탄 피복 내핵 입자를 교반하면서, 벤푸라카르브 원체 5부(유효성분량), 화이트카본(카프렉스#1120) 7부, 파라핀왁스(상품명「도요파락스 A40S」, 도소 가부시키가이샤, 염화파라핀, 염소 함유율 40%) 5부를 차례로 첨가하고, 점토(NO 점토)를 고형분으로 전체가 100부가 되도록 첨가하여, 실시예 6의 살충 살균 혼합 입제를 얻었다.6.5 parts of the ionomer-type aqueous urethane resin (brand name "Hyran AP-40 (F)", Dainippon Ingiga Chemical Co., Ltd., 22.5% of solid content) while rolling the obtained inner core particle (D) with a concrete mixer By spraying on the particle surface, the polyurethane film was formed in the surface, and it dried at 60 degreeC after that for 2 hours. While stirring the obtained polyurethane-coated inner core particles, 5 parts of benfuracarb element (active ingredient amount), 7 parts of white carbon (caprex # 1120), paraffin wax (brand name "Toyo Parax A40S", Toso Kabushiki Kaisha, chloride 5 parts of paraffin and 40% of chlorine content were added sequentially, and the clay (NO clay) was added so that the whole may be 100 parts with solid content, and the insecticidal sterilization mixed granulation of Example 6 was obtained.

실시예 7Example 7

프로베나졸 원체 24부(유효성분량), 벤푸라카르브 원체 2.5부(유효성분량), 벤토나이트(C벤트) 1.5부, 폴리비닐알코올(PVA 224) 1.5부를 가하고, 점토(NO 점토)를 상기 성분과 합하여 88부가 되도록 가하여 더 혼합하고, 물 18.8부 및 특수 파라핀계왁스(푸르닛 101Z) 6부를 첨가하여 혼합한 후, 바스켓류저(스크린 1.0㎜)를 이용하여 직경 1㎜, 어스펙트비 약 3의 원통형 내핵 입자를 얻고, 이를 60℃에서 1시간 건조하여 내핵 입자 (E)를 얻었다.24 parts of Provenazole original (active ingredient), 2.5 parts of Benfuracarb original (active ingredient amount), 1.5 parts of bentonite (C vent), and 1.5 parts of polyvinyl alcohol (PVA 224) were added, and clay (NO clay) was added to the above components. Add to 88 parts of water, and further mix, add 18.8 parts of water and 6 parts of special paraffin wax (Purnet 101Z), mix, and then use a basket reducer (screen 1.0 mm) to make a diameter of 1 mm and an aspect ratio of about 3 Cylindrical inner core particles of were obtained and dried at 60 ° C. for 1 hour to obtain inner core particles (E).

얻어진 내핵 입자 (E)를 콘크리트믹서로 전동시키면서, 수계 폴리우레탄 수지(상품명 「닛포라 2606」, 니폰폴리우레탄고교 가부시키가이샤, 고형분 40%) 2.6부를 내핵 입자의 표면에 스프레이함으로써, 표면에 폴리우레탄 피막을 형성하였다. 교반을 계속하면서, 벤푸라카르브 원체 2.5부(유효성분량) 및 화이트카본(상품명「시피리나아트 50S」, 시오노기 세이야쿠 가부시키가이샤)을 여러 차례로 나누어 번갈아 첨가한 후, 수계폴리우레탄수지(닛포란 2606) 2.6부를 스프레이하였다. 이를 60℃에서 1시간 건조하여, 실시예 7의 살충 살균 혼합 입제를 얻었다.While spraying the obtained inner core particle (E) with a concrete mixer, 2.6 parts of water-based polyurethane resins (brand name "Nippora 2606", Nippon Polyurethane Co., Ltd., 40% of solid content) are sprayed on the surface of an inner core particle, A urethane film was formed. While continuing stirring, 2.5 parts of benfuracarb element (active ingredient amount) and white carbon (brand name "Sipyrina art 50S", Shionogi Seiyaku Kabuki Kaisha) are added in turn and added in turn, and then the aqueous polyurethane resin ( Nipporan 2606) 2.6 parts were sprayed. This was dried at 60 degreeC for 1 hour, and the insecticidal sterilization mixed granulation of Example 7 was obtained.

비교예 1Comparative Example 1

프로베나졸 원체 12부(유효성분량), 벤푸라카르브 원체 2.5부(유효성분량), 벤토나이트(C벤토) 3부, 알파화전분(마츠노린 M) 2부, 화이트카본(톡시일 AL-1) 1.8부 및 점토(NO 점토)를 가하여 혼합하고, 물 24부를 첨가하여 혼합한 후, 바스켓 류저로 직경 1.2㎜, 어스펙트비가 약 3인 원통형 내핵 입자를 얻었다. 60℃에서 2시간 건조한 후, 콘크리트믹서로 전동시키면서, 폴리우레탄 수분산체(수퍼플렉스 130) 4부를 스프레이하여, 표면에 폴리우레탄 피막을 형성하고, 60℃에서 2시간 건조하여, 비교예 1의 혼합 입제 100부를 얻었다.12 parts of probenazole element (active ingredient amount), 2.5 parts of benfuracarb element (active ingredient amount), 3 parts of bentonite (C bento), 2 parts of alpha starch (matsunorin M), white carbon (methoxyyl AL-1) ) 1.8 parts and clay (NO clay) were added and mixed, 24 parts of water was added and mixed, and a cylindrical inner core particle having a diameter of 1.2 mm and an aspect ratio of about 3 was obtained with a basket holder. After drying at 60 ° C. for 2 hours, 4 parts of a polyurethane water dispersion (Superflex 130) was sprayed while rolling with a concrete mixer to form a polyurethane film on the surface, and dried at 60 ° C. for 2 hours, followed by mixing of Comparative Example 1 100 parts of granules were obtained.

비교예 2Comparative Example 2

프로베나졸 원체 24부(유효성분량), 벤푸라카르브 5부(유효성분량), 화이트카본(카프렉스#1120) 3.5부, 벤토나이트(C벤토) 3부, 폴리비닐알코올(PVA 224) 2부, 탄산칼슘 1.5부를 가하고, 더욱이 점토(NO점토)를 전체 100부가 되도록 가하여 혼합하고, 물 23.3부를 첨가하여 혼합한 후, 바스켓 류저로 직경 1㎜, 어스펙트비가 약 3인 원통형 내핵 입자를 얻고, 이를 60℃에서 2시간 건조하여, 비교예 2의 혼합 입제 100부를 얻었다.Probenazole original 24 parts (active ingredient amount), benfuracarb 5 parts (active ingredient amount), white carbon (Caprex # 1120) 3.5 parts, bentonite (C bento) 3 parts, polyvinyl alcohol (PVA 224) 2 parts 1.5 parts of calcium carbonate was added, and then 100 parts of clay (NO clay) was added and mixed, 23.3 parts of water was added and mixed, and then a cylindrical inner core particle having a diameter of 1 mm and an aspect ratio of about 3 was obtained with a basket holder. This was dried at 60 degreeC for 2 hours, and 100 parts of mixed granules of the comparative example 2 were obtained.

비교예 3Comparative Example 3

프로베나졸 원체 24부(유효성분량), 벤푸라카르브 원체 2.5부(유효성분량), 벤토나이트(C벤토) 3부, 폴리비닐알코올(PVA 224) 2부를 가하고, 더욱이 점토(NO 점토)를 가하여 혼합하고, 물 13.3부 및 특수 파라핀계 왁스(프루닛 101Z) 10부를 첨가하여 혼합하였다. 바스켓류저(스크린 1.0㎜)를 이용하여 원통형 내핵 입자를 얻고, 마르메라이저를 이용하여 어스펙트비가 약 1.5인 거의 구형으로 정립(整粒)한 후, 콘크리트믹서로 전동시키면서 벤푸라카르브 원체 2.5부(유효성분량)를 서서히 첨가하였다. 이를 60℃에서 2시간 건조하여, 비교예 3의 혼합 입제 100부를 얻었다.24 parts of Probenazole original (active ingredient), 2.5 parts of Benfuracarb original (active ingredient), 3 parts of bentonite (C bento), 2 parts of polyvinyl alcohol (PVA 224) were added, and clay (NO clay) was further added. 13.3 parts of water and 10 parts of special paraffin wax (Prunit 101Z) were added and mixed. Cylindrical inner core particles were obtained by using a basket reducer (screen 1.0 mm), and a marfurizer was formed into an almost spherical shape having an aspect ratio of about 1.5. Part (active ingredient amount) was added slowly. This was dried at 60 degreeC for 2 hours, and 100 parts of mixed granules of the comparative example 3 were obtained.

비교예 4Comparative Example 4

프로베나졸 원체 24부(유효성분량), 폴리비닐알코올(PVA224) 2부, 스테알린산마그네슘 3부, 더욱이 점토(NO 점토)를 가하여 혼합하고, 물 23.3부를 첨가하여 혼합한 후, 바스켓류저(스크린 1.0㎜)를 이용하여 직경 1㎜, 어스펙트비 약 3의 원통형 내핵 입자를 얻었다. 60℃에서 2시간 건조한 후, 콘크리트 믹서로 전동시키면서, 벤푸라카르브 원체 5부(유효성분량)를 서서히 첨가하여, 비교예 4의 혼합 입제 100부를 얻었다.After adding 24 parts of Probenazole original substance (active ingredient amount), 2 parts of polyvinyl alcohol (PVA224), 3 parts of magnesium stearate, and clay (NO clay), and adding and mixing 23.3 parts of water, Screen 1.0 mm) to obtain cylindrical inner core particles having a diameter of 1 mm and an aspect ratio of about 3. After drying at 60 ° C. for 2 hours, 5 parts (active ingredient amount) of benfuracarb was gradually added while rolling with a concrete mixer, and 100 parts of mixed granules of Comparative Example 4 were obtained.

비교예 5Comparative Example 5

화이트카본(톡시일 AL-1)에 벤푸라카르브 원체 2.5부(유효성분량)를 서서히 첨가하면서, 충분히 혼합한 후, 프로베나졸 원체 12부(유효성분량)를 가하고 혼합하여, 혼합물 A를 얻었다. 다음으로, 규사 82부를 혼합하면서, 폴리우레탄수분산체(수퍼플렉스 130) 4부를 적당량의 물에 희석한 것과 상기 혼합물 A를 혼합하여 균일하게 피복한 후, 60℃에서 2시간 건조하여, 비교예 5의 혼합 입제 100부를 얻었다.2.5 parts (effective amount) of benfuracarb element was slowly added to white carbon (methoxyyl AL-1), and after mixing enough, 12 parts (probe amount) of probenazole element were added and mixed, and mixture A was obtained. . Next, while mixing 82 parts of silica sand, 4 parts of polyurethane water dispersion (Superflex 130) was diluted in an appropriate amount of water, and the mixture A was mixed and uniformly coated, followed by drying at 60 ° C. for 2 hours, and Comparative Example 5 100 parts of mixed granules were obtained.

이상과 같이 하여 얻어진 실시예 1∼7 및 비교예 1∼5의 배합 조성을, 표 1∼표 3에 정리하여 나타낸다.The compounding compositions of Examples 1 to 7 and Comparative Examples 1 to 5 obtained as described above are collectively shown in Tables 1 to 3.

실시예 1Example 1 실시예 2Example 2 실시예 3Example 3 내핵입자Inner nuclear particles 프로베나졸 12부벤토나이트 3부α화 전분 2부점토 63부Probenazole 12 parts Bentonite 3 parts α-ized starch 2 parts Clay 63 parts 프로베나졸 24부벤토나이트 3부PVA 2부점토 52.2부Probenazole 24 parts Bentonite 3 parts PVA 2 parts Clay 52.2 parts 프로베나졸 24부벤토나이트 3부PVA 2부점토 52.2부Probenazole 24 parts Bentonite 3 parts PVA 2 parts Clay 52.2 parts 피복수지Coating resin 폴리우레탄수분산체 4부 (1.4부)4 parts of polyurethane water dispersion (1.4 parts) 아이오노머형수성우레탄 7부 (2.1부)Ionomer-type aqueous urethane 7 parts (2.1 parts) 폴리우레탄수분산체 8부 (2.4부)8 parts polyurethane dispersion (2.4 parts) 외층부Outer layer 벤푸라카르브 2.5부화이트카본 1.8부점토 나머지Ventura Carb 2.5 parts White Carbon 1.8 parts Clay Rest 탄산칼슘 1.5부벤푸라카르브 5부화이트카본 3.5부점토 나머지Calcium Carbonate 1.5 parts Benfuracarb 5 parts White Carbon 3.5 parts Clay Rest 벤푸라카르브 5부화이트카본 3부점토 나머지Ventura Carb Part 5 White Carbon Part 3 Clay Rest 합계Sum 100부                      100 copies 100부                      100 copies 100부                    100 copies

실시예 4Example 4 실시예 5Example 5 실시예 6Example 6 실시예 7Example 7 내핵 입자 Inner core particles 프로베나졸 24부벤푸라카르프 2.5부벤토나이트 3부PVA 2부점토 46.9부왁스 10부 (5부)Probenazole 24 parts Benfurakarpe 2.5 parts Bentonite 3 parts PVA 2 parts Clay 46.9 parts Wax 10 parts (5 parts) 프로베나졸 24부벤토나이트 3부PVA 2부점토 52.2부Probenazole 24 parts Bentonite 3 parts PVA 2 parts Clay 52.2 parts 프로베나졸 24부벤토나이트 3부PVA 2부점토 45.7부Probenazole 24 parts Bentonite 3 parts PVA 2 parts Clay 45.7 parts 프로베나졸 24부벤푸라카르브 2.5부벤토나이트 1.5부PVA 1.5부점토 58.5부왁스 6부 (3부)Probenazole 24 parts Benfuracarb 2.5 parts Bentonite 1.5 parts PVA 1.5 parts Clay 58.5 parts Wax 6 parts (3 parts) 피복수지Coating resin 초산비닐에멀전 4.5부 (2.4부)4.5 parts (2.4 parts) of vinyl acetate emulsion 락카형폴리우레탄수분산체 5부 (2.5부)Lacca-type Polyurethane Dispersion (5 parts) 아이오노머형수성 우레탄 6.5부 (1.46부)Ionomer-type aqueous urethane 6.5 parts (1.46 parts) 수계폴리우레탄수지 2.6부 (1.04부)Water-based polyurethane resin 2.6 parts (1.04 parts) 외층부 Outer layer 점토 나머지벤푸라카르브 2.5부Clay Restbenfuracarb 2.5 벤푸라카르브 5부화이트카본 3부점토 나머지Ventura Carb Part 5 White Carbon Part 3 Clay Rest 벤푸라카르브 5부화이트카본 7부왁스 5부점토 나머지Ventura Carb Part 5 White Carbon Part 7 Wax 5 Part Clay Rest 벤푸라카르프 2.5부화이트카본 나머지 Benpurakar 2.5 parts white carbon rest 피복수지 수계폴리우레탄수지 2.6부 (1.04부)Coating resin Water-based polyurethane resin 2.6 parts (1.04 parts) 합계Sum 100부            100 copies 100부           100 copies 100부           100 copies 100부             100 copies

비교예 1Comparative Example 1 비교예 2Comparative Example 2 비교예 3Comparative Example 3 비교예 4Comparative Example 4 비교예 5Comparative Example 5 내핵 입자 Inner core particles 프로베나졸 12부벤푸라카르브 2.5부벤토나이트 3부α화 전분 2부화이트카본 1.8부점토 나머지Probenazole 12 parts Benfururacarb 2.5 parts Bentonite 3 parts α-ized starch 2 parts White carbon 1.8 parts Clay Rest 프로베나졸 24부벤푸라카르브 5부화이트카본 3.5부벤토나이트 3부PVA 2부탄산칼슘 1.5부점토 61부Probenazole 24 parts Benfuracarb 5 parts White carbon 3.5 parts Bentonite 3 parts PVA 2 parts Calcium carbonate 1.5 parts Clay 61 parts 프로베나졸 24부벤푸라카르브 2.5부벤토나이트 3부PVA 2부점토 나머지왁스 10부 (5부)Probenazole 24 parts Benfuracarb 2.5 parts Bentonite 3 parts PVA 2 parts Clay Rest wax 10 parts (5 parts) 프로베나졸 24부PVA 2부스테알린산마그네슘 3부점토 나머지Probenazole 24 parts PVA 2 magnesium stearate 3 parts clay Rest 규사 82부Silica 82 피복수지Coating resin 폴리우레탄수분산체 4부 (1.4부)4 parts of polyurethane water dispersion (1.4 parts) 없음 none 없음 none 없음 none 폴리우레탄수분산체 4부 (1.4부)4 parts of polyurethane water dispersion (1.4 parts) 외층부 Outer layer 없음 none 없음 none 벤푸라카르브 2.5부Benfuracarb Part 2.5 벤푸라카르브 5부Benfuracarb Part 5 화이트카본 나머지벤푸라카르브 2.5부프로베나졸 12부White Carbon Rest Benfuracarb 2.5 parts Provenazole 12 parts 합계Sum 100부          100 copies 100부          100 copies 100부          100 copies 100부          100 copies 100부        100 copies

시험예 1 (용출시험)Test Example 1 (Dissolution Test)

실시예 1∼4 및 비교예 1∼5의 각 혼합 입제 160㎎을, 800㎖의 활성탄 처리수를 넣은 비이커(beaker)에 투입하였다. 소정 시간마다 비이커의 중앙부로부터 시험액을 채취하여, 고속 액체 크로마토그래피에 의해, 유효 성분의 함유량을 측정하고, 용출률을 산출하였다. 결과를 표 4에 나타낸다.160 mg of each mixed granule of Examples 1 to 4 and Comparative Examples 1 to 5 was charged into a beaker containing 800 ml of activated carbon treated water. Every predetermined time, the test liquid was extract | collected from the center part of the beaker, the content of the active ingredient was measured by high performance liquid chromatography, and the dissolution rate was computed. The results are shown in Table 4.

공시약제Disclosure 성분명Ingredient Name 용 출 률 (%)Dissolution Rate (%) 2일후2 days later 4일후4 days later 6일후6 days later 8일후8 days later 10일후10 days later 실시예 1Example 1 프로베나졸Probenazole 6.7 6.7 13.013.0 19.219.2 25.025.0 30.730.7 벤푸라카르브Benpuracarb 7.2 7.2 14.414.4 21.621.6 27.627.6 33.633.6 실시예 2Example 2 프로베나졸Probenazole 6.7 6.7 12.712.7 18.118.1 23.323.3 28.128.1 벤푸라카르브Benpuracarb 8.0 8.0 15.015.0 21.021.0 26.026.0 31.031.0 실시예 3Example 3 프로베나졸Probenazole 7.7 7.7 15.015.0 22.322.3 29.429.4 36.036.0 벤푸라카르브Benpuracarb 8.0 8.0 15.015.0 22.022.0 27.027.0 32.032.0 실시예 4Example 4 프로베나졸Probenazole 9.0 9.0 17.117.1 24.224.2 30.430.4 35.835.8 벤푸라카르브Benpuracarb 7.0 7.0 13.013.0 19.019.0 25.025.0 30.030.0 비교예 1Comparative Example 1 프로베나졸Probenazole 8.5 8.5 17.717.7 26.726.7 35.135.1 42.242.2 벤푸라카르브Benpuracarb 4.6 4.6 9.9 9.9 14.814.8 18.618.6 20.320.3 비교예 2Comparative Example 2 프로베나졸Probenazole 14.414.4 26.726.7 37.137.1 47.347.3 57.157.1 벤푸라카르브Benpuracarb 8.2 8.2 16.516.5 24.324.3 31.631.6 38.038.0 비교예 3Comparative Example 3 프로베나졸Probenazole 14.214.2 25.625.6 35.235.2 42.742.7 49.049.0 벤푸라카르브Benpuracarb 9.4 9.4 17.917.9 24.724.7 30.630.6 35.735.7 비교예 4Comparative Example 4 프로베나졸Probenazole 12.412.4 23.323.3 32.732.7 40.640.6 47.647.6 벤푸라카르브Benpuracarb 8.5 8.5 16.916.9 24.224.2 30.030.0 33.433.4 비교예 5Comparative Example 5 프로베나졸Probenazole 17.917.9 29.229.2 39.539.5 49.749.7 59.859.8 벤푸라카르브Benpuracarb 12.812.8 20.220.2 29.629.6 37.537.5 43.243.2

표 4의 결과로부터 알 수 있듯이, 본 발명에 따른 실시예 1∼4의 혼합 입제에서는, 벤푸라카르브가 빠르게 용출함과 함께, 프로베나졸이 서방성을 동반하여 용출하는 것을 알 수 있다.As can be seen from the results in Table 4, it can be seen that in the mixed granules of Examples 1 to 4 according to the present invention, benfuracarb rapidly elutes and provenazole elutes with sustained release.

상기 실시예에서는, 제 1 농약 활성 성분으로서 프로베나졸을, 제 2 농약 활성 성분으로서 벤푸라카르브를 예로 하여 설명하였지만, 본 발명은 이들 조합에 한정되는 것은 아니며, 그 밖의 농약 활성 성분의 조합에도 적용할 수 있는 것이다.In the above embodiment, the description has been made with the example of provenazole as the first pesticide active ingredient and benfuracarb as the second pesticide active ingredient, but the present invention is not limited to these combinations. It is also applicable to.

본 발명에 따르면, 혼합하여도 안정되게 사용할 수 있는 제 1 농약 활성 성분과 제 2 농약 활성 성분을 함유하는 농업용 혼합 입제에 있어서, 제 1 농약 활성 성분의 급격한 용출을 막으면서, 시용 직후부터 제 2 농약 활성 성분의 효과를 발현할 수 있는 농업용 혼합 입제를 제공할 수 있다. According to the present invention, in an agricultural mixed granule containing a first pesticide active ingredient and a second pesticide active ingredient which can be used stably even after mixing, the second pesticide is immediately released from the first application while preventing rapid elution of the first pesticide active ingredient. An agricultural mixed granule capable of expressing the effect of the pesticide active ingredient can be provided.

Claims (6)

혼합하여도 안정되게 사용할 수 있는 제 1 농약 활성 성분과 제 2 농약 활성 성분을 함유하는 농업용 혼합 입제(粒劑)로서,As an agricultural mixed granule containing the 1st pesticide active ingredient and the 2nd pesticide active ingredient which can be used stably even if mixed, 내핵 입자의 표면을 에멀젼 수지로 피복하고, 그 둘레에 외층부를 형성한 구조를 가지며, 제 1 농약 활성 성분이 주로 내핵 입자에 함유되어 있고, 제 2 농약 활성 성분이 주로 외층부에 함유되어 있으며,It has a structure which coat | covers the surface of an inner core particle with an emulsion resin, and formed the outer layer part around it, the 1st pesticide active ingredient is mainly contained in an inner core particle, the 2nd pesticide active ingredient is mainly contained in an outer layer part, 제 1 농약 활성 성분이 프로베나졸(Probenazole)이고, 제 2 농약 활성 성분이 벤푸라카르브(Benfuracarb), 피프로닐(Fipronil), 에토펜프록스(Ethofenprox), 푸라티오카르브(Furathiocarb), 카르보술판(Carbosulfan) 및 이미다크로프리드(Imidacloprid)로 이루어진 군에서 선택되는 적어도 한 종임을 특징으로 하는 농업용 혼합 입제.The first pesticide active ingredient is Probenazole, the second pesticide active ingredient is Benfuracarb, Fipronil, Ethofenprox, Furathiocarb, Agricultural granules, characterized in that at least one species selected from the group consisting of Carbosulfan and imidacloprid. 삭제delete 삭제delete 제 1항에 있어서, 프로베나졸의 함유량이 입제 전체에 대해 3∼70 중량% 임을 특징으로 하는 농업용 혼합 입제.The agricultural granulated granules according to claim 1, wherein the content of probenazole is 3 to 70% by weight based on the whole granules. 제 1항에 있어서, 프로베나졸의 함유량이 입제 전체에 대해 8∼70중량%임을 특징으로 하는 농업용 혼합 입제.The agricultural granulated granules according to claim 1, wherein the content of probenazole is 8 to 70% by weight based on the whole granules. 제 1 항, 제 4항 및 제 5항 중 어느 한 항에 있어서, 내핵 입자를 피복하는 에멀젼 수지가 폴리우레탄수지임을 특징으로 하는 농업용 혼합 입제.The agricultural mixed granulation according to any one of claims 1, 4 and 5, wherein the emulsion resin covering the inner core particles is a polyurethane resin.
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Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3746677B2 (en) * 2000-12-12 2006-02-15 三井化学株式会社 Sustained release agricultural chemicals
JP4677146B2 (en) * 2001-09-04 2011-04-27 三井化学アグロ株式会社 Coated sustained-release granules
TW200304772A (en) * 2002-03-08 2003-10-16 Meiji Seika Kaisha Fungicidal composition for control of rice plant disease
KR100676829B1 (en) 2003-01-27 2007-02-05 재단법인 한국화학시험연구원 Controlled release pesticidal granules coated with biodegradable polymer of low melting point or amorphousness and a process for the production thereof
FR2850576B1 (en) * 2003-02-05 2007-03-23 Ethypharm Sa COMPOSITION COMPRISING A MIXTURE OF ACTIVE INGREDIENTS AND PROCESS FOR PREPARING THE SAME
TW200500008A (en) * 2003-04-09 2005-01-01 Meiji Seika Kaisha Slow-releasable pesticide granules
JP2011026349A (en) * 2003-12-04 2011-02-10 Sumitomo Chemical Co Ltd Agrochemical granule
KR20070041709A (en) * 2004-06-04 2007-04-19 인바이로포커스 리미티드 Improvements in or relating to plant treatment agents
AU2006347294A1 (en) * 2005-12-22 2008-02-21 Syngenta Participations Ag Methods and composition for growth engineering and disease control
DE102006033723A1 (en) * 2006-07-21 2008-01-24 Bayer Technology Services Gmbh Formulations of multicomponent granules for active ingredients
JP2009073820A (en) * 2007-08-31 2009-04-09 Sumitomo Chemical Co Ltd Granular agrichemical composition
KR101570536B1 (en) * 2008-05-16 2015-11-19 수미토모 케미칼 컴퍼니 리미티드 Agrichemical granules
CN102657157A (en) * 2012-04-19 2012-09-12 天津市鑫卫化工有限责任公司 Probenazole granules and preparation method thereof
WO2015115476A1 (en) * 2014-01-29 2015-08-06 日本農薬株式会社 Method for controlling insect pests and controlling agent

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60202801A (en) * 1984-03-28 1985-10-14 Nippon Tokushu Noyaku Seizo Kk Granular substance of sustained release type
KR890001145A (en) * 1987-06-22 1989-03-18 아라이 기꾸지 Fluorescent lamp
JPH07149606A (en) * 1993-10-06 1995-06-13 Nissan Chem Ind Ltd Granular agent for agriculture and horticulture
US5652196A (en) * 1991-07-22 1997-07-29 Oms Investments, Inc. Timed release of water-soluble plant nutrients
JPH09315903A (en) * 1996-05-29 1997-12-09 Hokko Chem Ind Co Ltd Granular agrochemical having improved storage stability
JPH104783A (en) * 1996-06-19 1998-01-13 Chisso Corp Horticultural culture soil for raising seedling and raising seedling using the same
JPH10152387A (en) * 1996-11-18 1998-06-09 Sumitomo Chem Co Ltd Granular coated fertilizer containing agrochemical
WO1999063817A1 (en) * 1998-06-09 1999-12-16 Oms Investments, Inc. Precoated controlled release fertilizers and processes for their preparation

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60202801A (en) * 1984-03-28 1985-10-14 Nippon Tokushu Noyaku Seizo Kk Granular substance of sustained release type
KR890001145A (en) * 1987-06-22 1989-03-18 아라이 기꾸지 Fluorescent lamp
US5652196A (en) * 1991-07-22 1997-07-29 Oms Investments, Inc. Timed release of water-soluble plant nutrients
JPH07149606A (en) * 1993-10-06 1995-06-13 Nissan Chem Ind Ltd Granular agent for agriculture and horticulture
JPH09315903A (en) * 1996-05-29 1997-12-09 Hokko Chem Ind Co Ltd Granular agrochemical having improved storage stability
JPH104783A (en) * 1996-06-19 1998-01-13 Chisso Corp Horticultural culture soil for raising seedling and raising seedling using the same
JPH10152387A (en) * 1996-11-18 1998-06-09 Sumitomo Chem Co Ltd Granular coated fertilizer containing agrochemical
WO1999063817A1 (en) * 1998-06-09 1999-12-16 Oms Investments, Inc. Precoated controlled release fertilizers and processes for their preparation

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