KR100289552B1 - Pesticide preparation - Google Patents
Pesticide preparation Download PDFInfo
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- KR100289552B1 KR100289552B1 KR1019940007670A KR19940007670A KR100289552B1 KR 100289552 B1 KR100289552 B1 KR 100289552B1 KR 1019940007670 A KR1019940007670 A KR 1019940007670A KR 19940007670 A KR19940007670 A KR 19940007670A KR 100289552 B1 KR100289552 B1 KR 100289552B1
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- pesticide
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- imazosulfuron
- dimeron
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N25/00—Biocides, 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
- A01N25/12—Powders or granules
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N25/00—Biocides, 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
- A01N25/30—Biocides, 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 characterised by the surfactants
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, 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
- A01N43/74—Biocides, 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 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N47/00—Biocides, 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
- A01N47/08—Biocides, 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
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
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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
[발명의 명칭][Name of invention]
농약 입제Pesticide
[요약][summary]
[목적] 붕괴 확전성과 안정성이 우수한 농약입제의 제공[Purpose] Providing pesticide granules with excellent collapse stability and stability
[구성] 농약 활성 성분, 중량제, 폴리아크릴산염 및 디알킬술포숙신산염을 함유하는 것을 특징으로 하는 농약 입제.[Configuration] Agrochemical granules containing an active pesticide active ingredient, a weighting agent, a polyacrylate and a dialkylsulfosuccinate.
[효과] 본 발명의 농약 입제는 붕괴확전성과 농약 활성 성분의 보존안정성이 우수하다.[Effects] The pesticide granules of the present invention are excellent in disintegration proliferation and storage stability of active pesticides.
Description
[발명의 명칭][Name of invention]
농약 입제Pesticide
[발명의 상세한 설명]Detailed description of the invention
본 발명은 붕괴성이 우수한 농약 입제에 관한 것이다. 더욱 상세하게는 본 발명은 논에의 산포시에 수중에서 신속하게 붕괴, 확전(擴展) 하는 농약 입제에 관한 것이다. 본 발명의 제제는 살충, 살균, 제초등의 목적으로 농업분야에서 사용된다.The present invention relates to a pesticide granules excellent in disintegration. More specifically, the present invention relates to a pesticide granules which rapidly collapse and expand in water when spreading on rice fields. The formulation of the present invention is used in agriculture for the purpose of insecticide, sterilization, weeding and the like.
종래, 입제는 분제, 유제, 수화제 등과 함께 농업분야에서 흔히 사용되는 제제 형태이다(일본 식물 방역협회 발행, 농약 핸드북 1992 년판). 본 발명에서 사용되는 폴리아크릴산염은 농약 고형 제제의 붕괴조제로서 시판되고 있다. 또 디알킬 술포숙신산염은 표면 장력을 감소시키는 계면 활성제로서 공지되어 있다(산업도서(주) 발행, 계면활성제 편람, 발행일 소화 36 년 9 월 10 일). 그러나 폴리아크릴산염과 디알킬술포숙신산염을 함께 함유하고, 붕괴성이 우수한 농약입제는 알려져 있지 않다.Conventionally, granulation is a formulation form commonly used in the agricultural field together with powders, emulsions, hydrating powders, etc. (issued by the Japan Plant Protection Association, 1992 Pesticide Handbook). Polyacrylates used in the present invention are commercially available as disintegration aids for agrochemical solid preparations. Dialkyl sulfosuccinates are also known as surfactants for reducing surface tension (published by Industrial Co., Ltd., Handbook of Surfactants, September 10, 36). However, pesticide granules containing polyacrylate and dialkylsulfosuccinate together and having excellent disintegration are not known.
본 발명은 주로 논에 있어서의 벼재배를 위하여 사용되는 농약 입제를 제공한다.The present invention provides pesticide granulation mainly used for rice cultivation in rice fields.
입제를 논에 산포하면 입제는 수중에서 붕괴하고 확전하여 주약이 방출되고, 확산함으로써 약효를 나타낸다. 따라서 입제의 붕괴, 확전성은 우수한 약효를 위한 중요한 인자이다.When the granules are dispersed in rice fields, the granules disintegrate and expand in water, and the main medicine is released and diffused. Therefore, the disintegration and expansion of granules are important factors for good drug efficacy.
본 발명은 (1) 논에 산포하면 신속하게 물을 빨아들여 팽윤하고 용이하게 붕괴하므로써 농약활성 성분을 효율좋게 확전할 뿐만아니라, (2) 조립성이 좋고, (3) 농약활성 성분의 안정성이 우수하고, (4) 제조비용이 저렴한 농약 입제를 제공한다.The present invention (1) spreads the rice paddy rapidly, swells and easily collapses, thereby efficiently expanding the pesticide active ingredient, and (2) good granularity and (3) stability of the pesticide active ingredient. (4) To provide pesticide granules that are excellent and have low manufacturing costs.
상기 과제를 해결하기 위하여, 본 발명자들은 농원예분야, 의약분야, 식품분야에서 사용되는 수많은 보조제, 첨가제, 계면활성제, 용제 및 그것들의 조합에 관하여 검토한 결과, 폴리아크릴산염과 디알킬술포숙신산염을 가하여 제조한 농약 입제가 본 발명의 과제를 해결하는 것이라는 것을 알아내었다.In order to solve the above problems, the present inventors have studied a number of auxiliaries, additives, surfactants, solvents and combinations thereof used in agrohorticulture, medicine and food, and as a result, polyacrylates and dialkylsulfosuccinates. It was found that the pesticide granules prepared by adding the solution solve the problems of the present invention.
본 발명은 (1) 농약 활성 성분(농약 활성 성분이 이마조술푸론, 메페나세트 및 다이므론으로 구성됨은 제외한다), 중량제, 폴리아크릴산염 및 디알킬술포숙신산염을 함유하는 것을 특징으로 하는 농약입제 및 (2) 농약 활성 성분(농약 활성 성분이 이마조술푸론, 메페나세트 및 다이므론으로 구성됨은 제외한다), 폴리아크릴산염, 디알킬술포숙신산염, 중량제, 또 소망에 따라 계면활성제, 및 결합제를 혼합하여 조립하는 것을 특징으로 하는 상기 (1) 기재의 농약 입제의 제조방법에 관한 것이다.The present invention is characterized by containing (1) agrochemical active ingredients (except that the agrochemical active ingredients consist of imazosulfuron, mefenacet and dimeron), weighting agents, polyacrylates and dialkylsulfosuccinates. Pesticide preparations, and (2) pesticide active ingredients (except that the pesticide active ingredient consists of imazosulfuron, mefenacet and dimeron), polyacrylates, dialkylsulfosuccinates, weight agents, and as desired It relates to a method for producing a pesticide granules according to the above (1), wherein the surfactant and the binder are mixed and granulated.
상기 (1)기재의 농약 입제로서는, (3)농약 입제 전체에 대하여 폴리아크릴산염의 함량이 약 0.1 ∼ 10 %(중량비)이고, 디알킬술포숙신산염의 함량이 약 0.1-5 %(중량비)인 상기 (1)기재의 농약 입제 및 (4)농약 활성 성분이 이마조술푸론, 프레티라크롤, 다이므론 및 에스프로카르브로부터 선택되는 1 이상의 제초활성 성분인 상기 (1) 기재의 농약 입제(단, 농약 활성 성분이 이마조술푸론, 메페나세트 및 다이므론으로 구성됨은 제외한다)가 바람직하다.As the pesticide granulation according to the above (1), the content of the polyacrylate is about 0.1 to 10% (weight ratio) and the dialkyl sulfosuccinate content is about 0.1-5% (weight ratio) with respect to the whole pesticide granulation. Pesticide granulation according to the above (1), wherein the pesticide granulation according to the above (1) and (4) the active ingredient of the pesticide is at least one herbicidally active ingredient selected from imazosulfuron, pretilacrol, dimeron and esprocarb ( However, except that the pesticide active ingredient consists of imazosulfuron, mefenacet and dimeron).
농약 활성 성분은 한정되지 않는다. 단, 농약 활성 성분이 이마조술푸론, 메페나세트, 및 다이므론으로 구성됨을 제외한다. 예컨대 소프트 사이언스사(일본) 발행의 최신 농약 데이타 북 1989 년판이나 일본 식물 방역협회(일본) 발행의 농약 핸드북 1992 년판에 등재되어 있는 농약활성 성분을 들수가 있다.Pesticide active ingredients are not limited. Except that the pesticide active ingredient consists of imazosulfuron, mefenacet, and dimeron. For example, the active ingredient of a pesticide may be mentioned in the latest pesticide data book 1989 edition of Soft Science Corporation (Japan) and the pesticide handbook 1992 edition of Japan Plant Protection Association (Japan).
상기한 바와 같이 본 발명에 사용되는 농약활성 성분은 일반적으로 농약으로서 사용되는 것이면 어떤 것이라도 사용할 수가 있으나, 예컨대, 제초제, 살충제, 살균제 등이 사용된다.As described above, any pesticide active ingredient used in the present invention can be used as long as it is generally used as a pesticide. For example, herbicides, insecticides, fungicides and the like are used.
제초제의 구체예로서는 예컨대 하기의 (i) ∼(xiv) 등이 사용된다.As a specific example of herbicide, following (i)-(xiv) etc. are used, for example.
(i)페녹시계 제초제 ‥‥ 예를들면 2, 4-D, MCPA, MCPCA, MCPB, 클로메프로프(chlomeprop), 나프로아닐리드(naproanilide), DEH-112(N-부틸-(R)-2-[4-(2-플루오로-4-시아노페녹시)페녹시]프로피오네이트)등(i) phenoxy clock herbicides ‥‥ 2, 4-D, MCPA, MCPCA, MCPB, chlomeprop, naproanilide, DEH-112 (N-butyl- (R) -2 -[4- (2-fluoro-4-cyanophenoxy) phenoxy] propionate), etc.
(ii) 디페닐에테르계 제초제 ‥‥ 예를들면 클로르니트로펜(chlornitrofen), 클로로메톡시닐(chlormethoxynil), 비페녹스(bifenox) 등,(ii) diphenyl ether herbicides, such as chlornitrofen, chloromethoxynil, bifenox, etc .;
(iii) 카르바메이트계 제초제 ‥‥ 예를들면 스웹(swep), 티오벤카르브(thiobencarb), 에스프로카르브(esprocarb), 몰리네이트(molinate), 디메피페레이트(dimepiperate), 피리부티카르브(pyributycarb) 등,(iii) carbamate herbicides, e.g. swep, thiobencarb, esprocarb, molinate, dimepiperate, pyributicar Pyributycarb, etc.
(iv) 산아미드계 제초제 ‥‥ 예를들면, 프로파닐(propanil), 부타클로르(butachlor), 프레틸라클로르(pretilachlor), 브로모부티드(bromobutide), 메페나세트(mefenacet), HW-52(에토벤자미도(etobenzamido))(2′, 3′- 디클로로-4-에톡시메톡시벤즈아닐리드) 등,(iv) acidamide herbicides, e.g., propanil, butachlor, pretilachlor, bromobutide, mefenacet, HW-52 Etobenzamido) (2 ', 3'- dichloro-4-ethoxymethoxybenzanilide), etc.,
(v) 요소계 제초제 ‥‥ 예를들면, 다이므론(dymron) 등,(v) urea herbicides, e.g., dymron, etc.
(vi) 술포닐요소계 제초제 ‥‥ 예를들면, 벤술푸론-메틸(bensulfuron-Methyl), 이마조술푸론(N-(2-클로로이미다조[1, 2-a] 피리딘-3-일술포닐)-N′-(4, 6-디메톡시-2-피리미디닐)요소), 피라조술푸론-에틸(pyrazosulfuron-ethyl), 시노술푸론 등,(vi) sulfonyl urea herbicides, e.g., bensulfuron-methyl, imazosulfuron (N- (2-chloroimidazo [1,2-a] pyridin-3-ylsulfonyl) -N '-(4, 6-dimethoxy-2-pyrimidinyl) urea), pyrazosulfuron-ethyl, cynosulfuron, etc.,
(vii) 트리아진계 제초제 ‥‥ 예를 들면, 시메트린(simetryn), 프로메트린(prometryn), 디메타메트린(dimethametryn) 등,(vii) triazine herbicides; for example, simethrin, promethrin, dimethametry n, etc .;
(xiii) 다이아진계 제초제 ‥‥ 예를 들면, 벤타존(bentazone) 등,(xiii) diazine herbicides; for example, bentazone, etc.
(ix) 다이아졸계 제초제 ‥‥ 예를 들면, 옥사디아존(oxadiazon), 피라졸레이트(pyrazolate), 피라족시펜(pyrazoxyfen), 벤조페납(benzofenap) 등,(ix) diazole herbicides; for example, oxadiazon, pyrazolate, pyrazoxyfen, benzofenap, and the like.
(x) 디니트로아닐린계 제초제 ‥‥ 예를 들면, 트리플루랄린(thifluralin)등,(x) dinitroaniline herbicides; for example, trifluralin and the like,
(xi) 지방산계 제초제 ‥‥ 예를 들면, 달라폰(dalapon) 등,(xi) fatty acid herbicides, for example, dalapon, etc.
(xii) 유기인계 제초제 ‥‥ 예를 들면, 피페로포스(piperophos) 등,(xii) organophosphorus herbicides; for example, piperophos, etc.
(xiii) 니트릴계 제초제 ‥‥ 예를 들면, 클로르티아미드(chlorthiamid) 등,(xiii) nitrile herbicides, such as chlorthiamid,
(xiv) 기타의 제초제 ‥‥ 예를 들면, 디티오피르(dithiopyr) 등.(xiv) other herbicides; for example, dithiopyr and the like.
살충제, 살균제로서는 예를 들면 (i)∼(xiii) 등을 들수 있다.Examples of insecticides and fungicides include (i) to (xiii).
(i) 유기인계 살충제 ‥‥ 예컨대 펜티온(fenthion), 페니트로티온(fenitrothion), 피리미포스-메틸(pirimiphos-methyl), 다이아지논(diazinon), 퀴날포스(quinalphos), 이속사티온(isoxathion), 피리다펜티온(pyridaphenthion), 클로르피리포스-메틸(chlorpyrifos-methyl), 바미도티온(vamidothion), 말라톤(malathon), 펜토에이트(phenthoate), 디메토에이트(dimethoate), 디술포톤(disulfoton), 모노크로토포스(monocrotophos), 테트라클로르빈포스(tetrachlorvinphos), 클로로펜빈포스(chlorofenvinphos), 프로파포스(propaphos), 아세페이트(acephate), 살리티온(salithion), 트리클로르폰(trichlorphon), EPN등,(i) organophosphorus insecticides, e.g. ), Pyridaphenthion, chlorpyrifos-methyl, vamidothion, malathon, phenthoate, dimethoate, disulfotone ( disulfoton, monocrotophos, tetrachlorvinphos, chlorofenvinphos, propaphos, acephate, salityion, trichlorphon , EPN, etc.
(ii) 카르바메이트계 살충제 ‥‥ 예를 들면, 카르바릴(carbaryl), 메톨카르브(metolcarb), 이소프로카르브(isoprocarb), BPMC, 프로폭수르(propoxur), 크실릴카르브(xylylcarb), XMC, 카르보술판(carbosulfan), 벤푸라카르브(benfuracarb), 메토밀(methomyl), 티오디카르브(thiodicarb) 등(ii) Carbamate insecticides. For example, carbaryl, metolcarb, isoprocarb, BPMC, propoxur, xylylcarb ), XMC, carbosulfan, benfuracarb, methomyl, thiodicarb, etc.
(iii) 합성 피레드로이드계 살충제 ‥‥ 예를 들면, 시클로프로트린(cycloprothrin), 에토펜프록수(ethofenprox) 등,(iii) synthetic pyredoid insecticides. For example, cycloprothrin, ethofenprox, etc.,
(iv) 그외의 살충제 ‥‥ 예를 들면, 카르탭(cartap), 티오시클램(thiocyclam), 벤술탭(bensultap), 부프로페진(buprofezin), 카르보푸란(carbofuran), 푸라티오카르보(furathiocarb), 시아노펜포스(cyanofenphos) 등,(iv) Other pesticides ... for example, cartap, thiocyclam, bensultap, buprofezin, carbofuran, furathiocarbo ( furathiocarb, cyanofenphos and the like,
(v) 폴리할로 알킬티오계 살균제 ‥‥ 예를 들면, 캡탄(caftan) 등,(v) polyhaloalkylthio-based fungicides ... for example, captan, etc.
(vi) 유기염소계 살균제 ‥‥ 예를 들면, TPN, 프탈라이드(fthalide), 몽가아드(monguard) 등(vi) Organochlorine disinfectants .. For example, TPN, phthalide, monguard, etc.
(vii) 유기인계 살균제 ‥‥ 예를 들면, 에디펜포스(edifenphos), IBP(iprobenfos) 등,(vii) organophosphorus fungicides, e.g., edifenphos, IBP (iprobenfos), etc.
(viii) 벤조이미다졸계 살균제 ‥‥ 예를 들면, 티오파네이트-메틸(thiophanate-methyl), 베노밀(benomyl) 등,(viii) benzoimidazole-based fungicides; for example, thiophanate-methyl, benoyl, etc.
(ix) 카르복시아미드계 살균제 ‥‥ 예를 들면, 메프로닐(mepronil), 플루톨라닐(flutolanil), 테클로프탈람(tecloftalam), 펜시쿠론(pencycuron) 등.(ix) Carboxyamide disinfectants. For example, mepronil, flutolanil, tecloftalam, pencicuron and the like.
(x) 아실알라닌계 살균제 ‥‥ 예를 들면, 메탈락실(metalaxyl) 등,(x) acyl alanine fungicides ‥‥ For example, metalaxyl, etc.
(xi) N-헤테로환계 에르고스테롤 저해제 ‥‥ 예를 들면, 트리플루미졸(triflumizole) 등,(xi) N-heterocyclic ergosterol inhibitors .... For example, triflumizole, etc.,
(xii) 항생물질계 살균제 ‥‥ 예를 들면, 가스가마이신(kasugamycin), 발리다마이신(validamycin) A 등,(xii) antibiotic-based fungicides ... for example, kasugamycin, valididamycin A, etc.
(xiii) 그외의 살균제 ‥‥ 예를 들면, 프로베나졸(probenazole), 이소프로티올란(isoprothiolane), 트리시클라졸(tricyclazole), 피로퀼론(pyroquilon), 옥솔린산(oxolinic acid), 페림존(ferimzon), 이프로디온(iprodione) 등을 들수 있다.(xiii) Other fungicides ... e.g. probenazole, isoprothiolane, tricyclazole, pyroquilon, oxolinic acid, ferimzon ), Iprodione and the like.
그중에서도 특히, 예를들어, 이마조술푸론, 프레틸라크롤, 디메타메트린, 다이므론, 에스프로카르브, 메페나세트, DEH-112, 에토벤자미드, 모리네이트, 디메피페레이트, 피리부티카르브, 티오벤카르브등의 제초활성 성분을 바람직한 것으로서 들수가 있고, 또 KPP-314(코드명, 가껜제약(일본)), CH-900(코드명, 쥬가이 제약(일본)), MX-70906(코드명, 미쓰비시가세이(일본)) 등의 제초 활성 성분을 바람직한 것으로서 들수가 있다.Among them, for example, imazosulfuron, pretilacrol, dimethamethrin, dimron, esprocarb, mefenacet, DEH-112, etobenzamide, morinate, dimepiperate, pyributi Herbicide active ingredients, such as carb and thiobencarb, are mentioned as a preferable thing, and also KPP-314 (code name, Gabung Pharmaceuticals (Japan)), CH-900 (code name, Jugai Pharmaceutical (Japan)), MX Herbicide active ingredients, such as -70906 (code name, Mitsubishi Chemical Co., Ltd.), are mentioned as a preferable thing.
이상 기술한 농약성 성분은 단독으로 사용하여도 좋고 2 이상을 혼합하여 사용하여도 좋다.The pesticide components described above may be used alone or in combination of two or more thereof.
본 발명의 농약입제 전체에 대하여 농약 활성 성분의 사용량은 통상 약 0.1~50 %(중량), 보다 바람직하게는 약 0.3~35 %(중량) 정도이다.The use amount of the pesticide active ingredient is generally about 0.1 to 50% (by weight), and more preferably about 0.3 to 35% (by weight) with respect to the whole pesticide preparation of the present invention.
중량제는 통상 농약 고형제제에 사용되는 것이 좋으나 바람직한 예로서 점토, 활석, 산성 백토, 규조토, 탄산 칼슘, 제올라이트등을 들수 있다. 이것들은 단독으로 사용하여도 좋고, 병용하여도 좋다. 중량제의 사용량은 통상 45 ∼ 95 %(중량) 정도이며, 보다 바람직하게는 약 55 ∼ 75%(중량) 정도이다.The weight agent is generally used in agrochemical solid preparations, but preferable examples thereof include clay, talc, acidic clay, diatomaceous earth, calcium carbonate, zeolite and the like. These may be used independently and may be used together. The usage-amount of a weighting agent is about 45 to 95% (weight) normally, More preferably, it is about 55 to 75% (weight).
본 발명에서 사용되는 폴리아크릴산염으로서는, 구체적으로는 예를들어 폴리아크릴산나트륨염, 폴리아크릴산 칼륨염 등을 들수 있고, 그 사용량은 농약제제 전체에 대하여 통상 약 0.1~10 %(중량)정도이며, 보다 바람직하게는 약 0.5~5 %(중량) 정도이다.Specific examples of the polyacrylate used in the present invention include sodium polyacrylate salt, potassium polyacrylate salt, and the like, and the amount thereof is usually about 0.1 to 10% (weight) based on the whole pesticide preparation. More preferably, it is about 0.5-5% (weight) grade.
본 발명에서 사용되는 디알킬술포숙신산염의 알킬기는 탄소수 5 ∼ 20 정도의 것이 바람직하고, 구체적으로는 예를 들면 디옥틸술포숙신산 나트륨, 디노닐술포숙신산 칼륨등을 들수 있고, 그 사용량은 통상 약 0.1 ∼ 5%(중량), 보다 바람직하게는 약 0.2~2 %(중량) 정도이다.The alkyl group of the dialkylsulfosuccinate salt used in the present invention is preferably about 5 to 20 carbon atoms, and specific examples thereof include sodium dioctylsulfosuccinate, potassium dinonylsulfosuccinate, and the like. It is about 5% (weight), More preferably, it is about 0.2 to 2% (weight).
소망에 따라 추가의 다른 첨가제, 예를 들면 결합제, 계면활성제 등을 사용하여도 좋다.If desired, further other additives may be used, such as binders, surfactants and the like.
결합제로서는 농약 분야에서 통상 사용되는 결합제라도 좋으나, 특히 벤토나이트, 덱스트린이 바람직하다. 이것들은 단독으로 사용하여도 좋고, 병용하여도 좋다. 결합제의 사용량은 통상 약 1 ∼ 50 %(중량), 보다 바람직하게는 약 2 ∼ 30 %(중량)이다.The binder may be a binder commonly used in the pesticide field, but bentonite and dextrin are particularly preferable. These may be used independently and may be used together. The amount of the binder used is usually about 1 to 50% by weight, more preferably about 2 to 30% by weight.
계면활성제로서는 비이온성, 음이온성, 양이온성 및 양성이온성의 어느것이라도 좋으나, 통상은 비이온성 및/또는 음이온성의 것이 바람직하다. 적당한 비이온성 계면활성제로서는 예컨대 라우릴알콜, 스테아릴알콜, 올레일알콜등의 고급알콜인 에틸렌옥시드부가물 ; 이소옥틸페놀, 노닐페놀 등의 알킬페놀의 에틸렌옥시드 부가물 ; 부틸나프톨, 옥틸나프톨등의 알킬나프톨의 에틸렌옥시드부가물 ; 팔미트산, 스테아르산, 올레산 등의 고급지방산의 에틸렌옥시드 부가물 ; 스테아린인산, 디라우릴인산등의 모노 또는 디알킬 인산의 에틸렌옥시드부가물 ; 도데실아민, 스테아르산 아미드의 아민에 에틸렌옥시드를 중합부가시킨 것 ; 소르비탄 등의 다가 알콜의 고급 지방산 에스테르 및 그의 에틸렌옥시드 부가물 ; 에틸렌옥시드와 프로필렌옥시드의 중합 부가물 등을 들수 있다. 적당한 음이온성 계면 활성제로서는 예컨대 라우릴 황산나트륨, 올레일알콜황산 에스테르아민염등의 알킬 황산 에스테르염 ; 술포숙신산, 디옥틸 에스테르나트륨, 2 -에틸헥센술폰산 나트륨등의 알킬술폰산염 ; 이소프로필나프탈렌술폰산나트륨, 메틸렌비스나프탈렌술폰산나트륨, 리그닌술폰산 나트륨, 도데실벤젠술폰산나트륨 등의 아릴술폰산염 등을 들수 있다.The surfactant may be any of nonionic, anionic, cationic and zwitterionic, but usually nonionic and / or anionic. Suitable nonionic surfactants include, for example, ethylene oxide adducts which are higher alcohols such as lauryl alcohol, stearyl alcohol and oleyl alcohol; Ethylene oxide adducts of alkylphenols such as isooctylphenol and nonylphenol; Ethylene oxide addition products of alkyl naphthols, such as butyl naphthol and octyl naphthol; Ethylene oxide adducts of higher fatty acids such as palmitic acid, stearic acid and oleic acid; Ethylene oxide adducts of mono or dialkyl phosphoric acid such as stearic acid and dilauryl phosphoric acid; Polymerized addition of ethylene oxide to amines of dodecylamine and stearic acid amide; Higher fatty acid esters of polyhydric alcohols such as sorbitan and ethylene oxide adducts thereof; The polymerization adduct of ethylene oxide and a propylene oxide, etc. are mentioned. Examples of suitable anionic surfactants include alkyl sulfate ester salts such as sodium lauryl sulfate and oleyl alcohol sulfate esteramine salts; Alkyl sulfonates such as sulfosuccinic acid, sodium dioctyl ester and sodium 2-ethylhexene sulfonate; And aryl sulfonates such as sodium isopropyl naphthalene sulfonate, sodium methylenebisnaphthalene sulfonate, sodium lignin sulfonate and sodium dodecylbenzene sulfonate.
계면 활성제의 사용량은 일률적으로 말할 수 없으나, 본 발명의 제제 전체에 대하여 통상 0.1 ∼ 10 %(중량), 바람직하게는 0.5 ∼ 5 %(중량) 정도이다.Although the usage-amount of surfactant cannot be said uniformly, it is 0.1-10% (weight) normally with respect to the whole formulation of this invention, Preferably it is about 0.5 to 5% (weight).
본 발명의 농약 입제는 자체 공지의 방법에 의해서 용이하게 제조된다. 예컨대 농약 활성 성분, 폴리아크릴산염, 디알킬술포숙신산염, 중량제, 추가로 소망에 따라 계면활성제, 및 결합제를 혼합하여 조립함으로써 수행된다. 통상은 성분을 물과 함께 혼화하고, 압출조립하여 건조시킴으로써 제조한다.The pesticide granules of the present invention are easily produced by a method known per se. For example, it is carried out by mixing and assembling agrochemical active ingredients, polyacrylates, dialkylsulfosuccinates, weighting agents, further surfactants, and binders as desired. It is usually prepared by mixing the components with water, extruding and drying.
본 발명의 농약 입제의 사용방법의 바람직한 예로서는 손으로 산포하거나, 산립기나 단관분두(短管噴頭)가 부착된 동력 산포기 등의 농기구를 사용하여 실시된다. 실시량은 주약 함량에 따라 다르나, 입제로서, 10 아르당 1 ∼ 3 kg가 바람직하다.As a preferable example of the method of using the pesticide granulation of the present invention, it is carried out using a farming machine such as a hand spreader or a power spreader with a granulator or a single pipe branch. Although the amount varies depending on the main drug content, 1-3 kg per 10 ar is preferable as a granule.
본 발명의 농약 입제는 수중증에서의 붕괴 확전성이 우수하고 농약 활성 성분의 보존 안정성이 우수하다.The pesticide granules of the present invention are excellent in collapse propagation in aquatic disease and excellent in storage stability of active pesticide ingredients.
이하에 실시예 및 시험예를 들어서 본 발명을 더 상세히 설명하겠으나, 본 발명은 이것들로 한정되는 것은 아니다.Although an Example and a test example are given to the following, this invention is demonstrated in more detail, but this invention is not limited to these.
[실시예 1]Example 1
소형 니더에 탄산칼슘 671.94 g, 이마조술푸론 원체(순도 98 %) 3.06 g, 토키사논 GR31A(폴리아크릴산염 약 40 % 수용액, 상요가세이(일본)) 20 g, 삼모린 OT-70(소듐 디옥틸술포숙시네이트 약 70 % 수용액, 상요가세이제) 5 g, 벤토나이트 300 g을 순차적으로 투입하고, 20분간 혼합한 후, 수돗물 150 ml을 가하여 10분간 반죽하였다. 반죽물을 압출형 조립기(입경 0.8 mm)로 조립하고, 유동층 건조기로 건조후, 체에 통과시켜 0.3 ∼ 1.7 mm(체 메쉬)의 입제 약 800 g을 얻었다.To small kneader 671.94 g of calcium carbonate, imazosulfuron original (purity 98%) 3.06 g, tokisanone GR31A (approximately 40% aqueous solution of polyacrylate, Sangyoseisei (Japan)), samoline OT-70 (sodium About 5% of dioctylsulfosuccinate solution and 5 g of bentonite) were sequentially added and mixed for 20 minutes, and then 150 ml of tap water was added to knead for 10 minutes. The dough was granulated in an extrusion granulator (0.8 mm in diameter), dried in a fluid bed dryer, and passed through a sieve to obtain about 800 g of granules of 0.3 to 1.7 mm (sieve mesh).
[실시예 2]Example 2
실시예 1과 동일하게 하여 하기 원료를 사용하여 2종류의 입제를 얻었다.In the same manner as in Example 1, two kinds of granules were obtained using the following starting materials.
[시험예][Test Example]
(1) 보존 안정성(1) storage stability
상기 실시예에서 얻어진 입제를 40℃에서 1개월, 2개월 및 3개월 및 실온에서 1년 6개월 보존하여 입제에 함유되어 있는 농약활성성분의 잔존율을 측정하였다.The granules obtained in the above examples were stored at 40 ° C. for 1 month, 2 months and 3 months, and at room temperature for 1 year and 6 months to measure the residual ratio of the pesticide active ingredient contained in the granules.
(가) 실시예 2(1)의 입제(A) Granulation of Example 2 (1)
[표 1]TABLE 1
(나) 실시예 2(2)의 제제(B) Formulation of Example 2 (2)
[표 2]TABLE 2
(2) 붕괴확전성 시험(2) collapse probability test
직경 9 cm의 시험 접시에 3도 경수 50 cc를 넣고 입제 3 개를 투하하고, 입제의 원형이 흔적없이 사라지는 시간을 측정한다. 그리고 투하 30분후의 확전면적을 측정한다.50 cc of 3 degree hard water is added to a 9 cm diameter test dish, and 3 granules are dropped, and the time when the granules of the granules disappear without a trace is measured. The area of expansion after 30 minutes is measured.
[표 3]TABLE 3
상기 시험 결과로부터 본 발명의 입제가 경도가 높은 수중에서도 붕괴확전성이 우수하고 농약활성 성분의 보존 안정성이 우수한 제제인 것을 알 수 있다.From the above test results, it can be seen that the granules of the present invention are excellent in disintegration proliferation even in water of high hardness and excellent in storage stability of the agrochemical active ingredient.
Claims (4)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP93-85043 | 1993-04-13 | ||
| JP5085043A JPH06298603A (en) | 1993-04-13 | 1993-04-13 | Granular agrichemical |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019940016766A Division KR100408912B1 (en) | 1993-04-13 | 1994-07-12 | Pesticide preparation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR940023358A KR940023358A (en) | 1994-11-17 |
| KR100289552B1 true KR100289552B1 (en) | 2001-11-30 |
Family
ID=13847660
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019940007670A Expired - Lifetime KR100289552B1 (en) | 1993-04-13 | 1994-04-12 | Pesticide preparation |
| KR1019940016766A Expired - Fee Related KR100408912B1 (en) | 1993-04-13 | 1994-07-12 | Pesticide preparation |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019940016766A Expired - Fee Related KR100408912B1 (en) | 1993-04-13 | 1994-07-12 | Pesticide preparation |
Country Status (3)
| Country | Link |
|---|---|
| JP (1) | JPH06298603A (en) |
| KR (2) | KR100289552B1 (en) |
| TW (1) | TW259689B (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1995031900A1 (en) * | 1994-05-24 | 1995-11-30 | Nippon Shinyaku Co., Ltd. | Pesticide composition, production process, and pesticidal preparation |
| US5512186A (en) * | 1995-04-28 | 1996-04-30 | Betz Laboratories, Inc. | Method for inhibiting microbial adhesion on surfaces |
| US5607597A (en) * | 1995-04-28 | 1997-03-04 | Betzdearborn Inc. | Method for enhancing biocidal activity |
| WO1997003558A1 (en) * | 1995-07-21 | 1997-02-06 | Nissan Chemical Industries, Ltd. | Solid preparation for paddy field and method for the application thereof |
| JPH09118602A (en) * | 1995-08-18 | 1997-05-06 | Nippon Kayaku Co Ltd | Water surface-floatable agrochemical preparation |
| US5635447A (en) * | 1996-03-22 | 1997-06-03 | Donlar Corporation | Polyorganic acids and their analogues to enhance herbicide effectiveness |
| US6241898B1 (en) | 1996-04-19 | 2001-06-05 | Betzdearborn Inc. | Method for inhibiting microbial adhesion on surfaces |
-
1993
- 1993-04-13 JP JP5085043A patent/JPH06298603A/en active Pending
-
1994
- 1994-03-19 TW TW083102395A patent/TW259689B/zh not_active IP Right Cessation
- 1994-04-12 KR KR1019940007670A patent/KR100289552B1/en not_active Expired - Lifetime
- 1994-07-12 KR KR1019940016766A patent/KR100408912B1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| KR100408912B1 (en) | 2004-12-23 |
| TW259689B (en) | 1995-10-11 |
| JPH06298603A (en) | 1994-10-25 |
| KR940023358A (en) | 1994-11-17 |
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