KR800000648B1 - Herbicidal composition - Google Patents

Herbicidal composition Download PDF

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KR800000648B1
KR800000648B1 KR7401084A KR740001084A KR800000648B1 KR 800000648 B1 KR800000648 B1 KR 800000648B1 KR 7401084 A KR7401084 A KR 7401084A KR 740001084 A KR740001084 A KR 740001084A KR 800000648 B1 KR800000648 B1 KR 800000648B1
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weeds
triazine
carbamate
methylthio
rice
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이찌로오 기무라
요시오 이시이
기요시 다기다
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모찌쯔 기기다시
구미아이가가구고교 가부시기가이샤
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Abstract

Herbicidal compd. contg. S-benzyl-N, N-dialkylthiol carbamate≮I; R = alkyl, X = halogen, methyl≉andphenoxy conpd., salt, ester of 2-methylthio-4,6-bisalkylamino-s- triazine of II was prepd. Thus, mixt. of s-(p-bromobenzyl)-N-N-dimethylthiol carbamate 5 % 2-(2-methyl-4,-chlorophenoxy)propionicacid aryl ester 1 %, 2-methylthio-4 ,6-bis-ethylamino-s-triazine 1 %, lognin sodium sulfonate 2 %, white carbon 5 % and bentonite 86 % knead with water, dried and granulated to give title compd. of 14-32 mesh.

Description

제초제 조성물Herbicide composition

본 발명은 하기 일반식(I)의 S-벤질-N,N-디알킬티올 카르바메이트와 하기 일반식(II)의 페녹시계 화합물이나, 그 염, 또는 에스테르 및 2-메틸티오-4,6-비스알킬아미노-S-트리아진과의 혼합물을 유효성분으로 함유하는 것을 특징으로 하는 제초제 조성물에 관한 것이다.The present invention relates to S-benzyl-N, N-dialkylthiol carbamate of the general formula (I) and a phenoxy compound of the general formula (II), salts or esters thereof, and 2-methylthio-4, A herbicidal composition comprising a mixture with 6-bisalkylamino-S-triazine as an active ingredient.

Figure kpo00001
Figure kpo00001

상기 식에서,Where

R는 알킬기,R is an alkyl group,

R′는 알킬렌기,R ′ is an alkylene group,

X는 할로겐원자 또는 메틸기,X is a halogen atom or a methyl group,

X′는 염소원자 또는 메틸기를 나타낸다.X 'represents a chlorine atom or a methyl group.

본 발명의 목적은 논에 발생하는 들피 등의 1년생인 여러가지 잡초, 쇠털골 등의 숙근생(宿根生) 잡초, 올미와 금방동산이 등의 다년생 잡초를 방제하고, 논에 해를 이르키지 않고 적용할 수 있고, 또 밭에 발생하는 들피, 바랭이 등의 화본과(禾本科) 잡초, 어귀, 명아주 등의 광엽(廣葉) 잡초, 금방동산이 등의 다년생 잡초를 방제하고, 콩, 목화, 옥수수 등의 유용작물에 해를 주지 않는 안전한 제초제 조성물을 제공하는데 있다. 따라서, 본 발명의 제초제 조성물은 1년생 잡초의 거의 모든 초본류(草本類)를 방제하고, 또 다년생 잡초에 대하여서도 유효하며 유용작물에 대한 안정성을 높인 것이다.An object of the present invention is to control various perennial weeds such as wild grasses, etc. that occur in paddy fields, yearly weeds such as ox bone, perennial weeds such as snares and geumbangdongi, without causing harm to rice fields. It can be applied to the control of perennial weeds such as wild grasses such as wild grass, barley, weed, broadleaf weeds such as estuaries, and mallow wine, and Geumbangsanyi. The present invention provides a safe herbicide composition that does not harm useful crops. Therefore, the herbicide composition of the present invention is to control almost all herbaceous plants of annual weeds, and is effective against perennial weeds and enhances stability against useful crops.

논에 있어서, 잡초는 발생 초기, 즉 써래질 당시에서부터 모를 심은 다음 약 2주간에 발생하는 것이며, 이 시기는 농번기로서 잡초 방제에는 손이 미치지 못하는 실정이다. 또한, 현재 시판되고 있는 각종의 제초제는 잡초의 발생 초기에는 유효하나, 모내기 10일을 지나면 제초효과가 떨어져 거의 제초의 목적을 달성할 수가 없다.In rice fields, weeds occur at the beginning of development, that is, about two weeks after planting at the time of harvesting, and this time is the agricultural season, which is out of reach of weed control. In addition, various herbicides currently on the market are effective in the early stages of weed development, but after 10 days of weeding, the herbicidal effect is poor and almost no purpose of weeding can be achieved.

또, 밭에 있어서의 잡초방제에는 카르바메이트계의 화합물, 우레아계의 화합물, 트리아진계의 화합물 등이 사용되고 있으나, 토양 중의 수분, 잡초의 종류, 작물의 종류 등의 문제로 해서 밭의 잡초를 완전히 방제하는 것이 불가능하였다.Carbamate-based compounds, urea-based compounds, triazine-based compounds and the like are used for weed control in the field. However, weeds in the field may be removed due to problems such as moisture in the soil, types of weeds, types of crops, and the like. It was impossible to control completely.

이와 같이, 이미 알려진 제초제에서는 이러한 요구를 충족시킬 만한 것이 없다. 또, 농업에 있어서의 노동력 부족과 모심을 때의 합리적인 노동력 분배 때문에, 1회의 처리로서 모든 시기에 발생하는 잡초의 방제, 즉 처리적 기의 폭이 넓은 것 및 밭의 잡초를 정확하게 방제하는 제초제의 출현이 요망되고 있다.As such, there is no known herbicide to meet this need. In addition, because of labor shortage in agriculture and reasonable labor distribution at the time of planting, we control of weed which occurs at all time as one treatment, that is, wide range of processing period and herbicide to control weed of field correctly An appearance is desired.

그러나, 본 발명의 제초제 조성물은 이러한 요망을 충분히 충족시킬 수 있는 것이다.However, the herbicide composition of the present invention is one that can sufficiently satisfy these requirements.

본 발명에서 사용되는 S-벤질티올카르바메이트는 들피, 쇠털골 등의 화분과 잡초에 대하여 방제효과가 우수하다. 즉, 발생 초기에 사용할 경우에는, 10아아르당 500g 이상을 사용하면 들피, 쇠털골을 방제할 수 있으나, 1년생 풀종류 중, 특히 여귀, 명아주, 털비름 등의 광엽 또는 금방동산이 등의 다년생 잡초에 대한 효과가 약하다.S-benzylthiolcarbamate used in the present invention is excellent in the control effect against pollen and weeds, such as wild grass, chaff bone. In other words, when used at the beginning of the development, the use of 500g or more per 10 are used to control the hulls and cow bones, but among the annual grass species, especially perennials such as broadleaf or jinbangdong, such as larvae, myeongju, hair agar The effect on weeds is weak.

또, 밭에 사용할 때에는 약량을 상당히 대량으로 사용하지 않으면 안된다. 한편, 식물 호르몬 작용을 가진 페녹시계 화합물은 잡초의 뿌리나 줄기 및 잎 등의 식물의 모든 부분에서 흡수되어 살초(殺草) 작용을 나타낸다. 즉, 이미 발생된 잡초에 농도 100-1,000ppm의 농도의 것을 줄기나 잎에 살포함으로써, 살포, 1주간 후에는 내크로시스(세포궤사(細胞潰死)를 동반하여 고사시킨다. 또, 잡초발아전(發芽前)이면 정지(整地)된 토양 표면에 10아아르당 유효성분으로서 50g 이상 처리함으로써 잡초의 발생을 완전히 억제할 수 있으나, 잡초와 유용(有用) 식물간의 선택성의 폭이 좁고, 항상 약해가 발생하고 있다. 또, 2-메틸티오-4,6-비스알킬아미노-S-트리아진은 잘 흡수되는 제초제이며, 광합성저해(光合成沮害)에 의해서 잡초를 고사시키거나, 또는 발아를 억제한다. 또, 잡초의 엽령(葉令)에 의해 관찰한 처리 적기의 폭은 들피일 때에는, 발아시에서 1엽기의 발생 초기에는 높은 효과를 나타내나, 3엽기 이후에서는 제초효과가 약하며, 고온에서는 가끔 논에 심은 벼와 밭에 심은 벼 등의 유용작물에 대하여 약해를 일으킬 때가 있다. 또, 밭에 있어서는 10아아르당 200g 이상으로 대단히 많은 약량을 처리하지 않으면 안된다.In addition, when you use it for a field, you must use a considerable quantity of medicine. On the other hand, the phenoxy clock compound having a plant hormone action is absorbed from all parts of the plant, such as the roots, stems and leaves of the weeds and exhibits a herbicide action. That is, by spraying the stem or leaves with a concentration of 100-1,000 ppm to the weeds that have already been generated, after 1 week of spraying, the cells are killed with acrosis (cell death). In the former case, the treatment of weeds can be completely suppressed by treating 50 g or more as an active ingredient per 10 ares on the surface of the suspended soil, but the selectivity between weeds and useful plants is narrow and always weak. In addition, 2-methylthio-4,6-bisalkylamino-S-triazine is a well absorbed herbicide and kills weeds or inhibits germination by photosynthesis inhibition. In addition, the width of the treatment bandit observed by weed leaf age shows a high effect at the beginning of the first stage of germination during germination, but weak herbicidal effect after the third leaf stage, and at high temperatures. Sometimes rice planted in rice fields and rice planted in fields There are times when it is harmful to useful crops such as etc. In addition, in the field, a very large amount must be treated at more than 200 g per 10 ares.

또한, 본 발명자 등은, S-벤질티올카르바메이트의 결점을 극복하기 위하여 각종의 연구를 한 결과, 이미 S-벤질티올카르바메이트와 페녹시계 화합물과의 혼합에 의한 제초제 조성물 S-벤질티올카르바메이트와 2-메틸티오-4,6-비스알킬아미노-S-트리아진과의 혼합에 의한 제초제 조성물을 명확하게 하였으나, 전자는 S-벤질티올 카르바메이트와 페녹시계 화합물의 효과에 의하여 화본과, 광엽, 다년생 잡초의 모든 초본류를 방제할 수 있게 되었으나 논에 있어서, 우세하게 번창하는 올미에는 효과가 약하며, 또 벼가 발아한 초기에는 약해가 생길 때가 있다.In addition, the present inventors have conducted various studies to overcome the drawbacks of S-benzylthiolcarbamate, and as a result, herbicide composition S-benzylthiol by mixing S-benzylthiolcarbamate and a phenoxy compound The herbicide composition by mixing carbamate and 2-methylthio-4,6-bisalkylamino-S-triazine was clarified, but the former was changed by the effect of S-benzylthiol carbamate and phenoxy compound. It is now possible to control all herbaceous plants of broad-leaved, broadleaf, and perennial weeds, but in rice fields, the prevailing Olme is less effective, and there are times when the rice germinates.

후자일 때에도 화본과, 광엽, 다년생 잡초의 모든 초본류를 방제할 수 있으나, 전자와 같이 올미 등의 후육업(厚肉葉)잡초에 대하여서는 효과가 약하고, 고온일 때에는 약해가 생기는 수가 있다.Even in the latter case, all herbaceous flowers, broadleaf, and perennial weeds can be controlled. However, as in the former, the effect is weak against thick-leaved weeds such as snares, and at high temperatures, weaknesses may occur.

이와 같은 것을 고려하여 여러가지의 검토를 행한 결과, 상기와 같은 결점을 극복하고, 거의 모든 논의 잡초를 방제하는 것과, 처리시기를 대폭적으로 연장할 수 있게 하고, 특히 종래 방제가 곤란하였던 올미의 방제를 가능하게 한 것은 대단히 의의깊은 것이다. 또 밭에 있어서는 약량을 대폭적으로 감소시킬 수 있는 것과, 너도방동산이, 향무자를 방제하는 등의 효과 및 경제적으로 유리한 제초제 조성물을 발견한 것이다. S-벤질티올카르바메이트계 화합물로서는, S-(P-브로모벤질)-N-N-디메틸티올카르바메이트(이하 BMC라고 함), S-(P-클로로벤질)-N,N-디메틸티올카르바메이트(이하 CBEC라고 함), S-(P-메틸벤질)-N,N-디이소프로필티올카르바메이트(이하 MBIC라고 함)이 있고, 페녹시계 화합물로서는 2,4-디클로로페녹시초산(이하 2,4-D라고 함), 2-(2-메틸-4-클로로페녹시)프로피온산(이하 MCPP라고 함), 2-메틸-4-클로로페녹시낙산(이하 MCPB라고 함)등의 염류 또는 에스테르가 있고 2-메틸티올-4,6-비스알킬아미노-S-트리아진으로서는, 2-메틸티오-4,6-비스-에틸아미노-S-트리아진(이하 MES라고 함), 2-메틸티오-4,6-비스 이소프로필아미노-S-트리아진(이하 MIS라고 함)을 들 수 있다.As a result of various studies in consideration of the above, it is possible to overcome the above-mentioned shortcomings, to control almost all rice weeds, and to prolong the treatment time significantly, and to prevent the control of Olme, which was difficult to control in the past. Enabling is very significant. In addition, in the field, it has been found that herbicide compositions that can significantly reduce the amount of the drug, and that the beta-banging property controls the perfume, and are advantageous economically. Examples of the S-benzyl thiol carbamate-based compound include S- (P-bromobenzyl) -NN-dimethylthiolcarbamate (hereinafter referred to as BMC) and S- (P-chlorobenzyl) -N, N-dimethylthiol Carbamate (hereinafter referred to as CBEC) and S- (P-methylbenzyl) -N, N-diisopropylthiolcarbamate (hereinafter referred to as MBIC). The phenoxy compound is 2,4-dichlorophenoxy. Acetic acid (hereinafter referred to as 2,4-D), 2- (2-methyl-4-chlorophenoxy) propionic acid (hereinafter referred to as MCPP), 2-methyl-4-chlorophenoxy butyric acid (hereinafter referred to as MCPB), etc. Salts or esters of 2-methylthiol-4,6-bisalkylamino-S-triazine, 2-methylthio-4,6-bis-ethylamino-S-triazine (hereinafter referred to as MES), 2-methylthio-4, 6-bis isopropylamino-S-triazine (henceforth MIS) is mentioned.

본 발명의 제초제 조성물의 유효성분인 S-벤질티올카르바메이트, 페녹시계 화합물 및 트리아진계 화합물의 혼합약량은 제각기의 단계로 사용할 경우보다 현저히 감소시켜서 사용함은 말할 나위도 없거니와, 제일 바람직한 혼합범위는 중량비로 S-벤질티올카르바메이트 : 페녹시계 화합물 : 트리아진계 화합물의 비가 1 : 0.01-0.3 : 0.01-0.5이며, 10아아르당의 사용량은 방제할 밭이나, 작물의 상태에 따라 달라지나 논일 때에는 50-300g : 10-60g : 10-70g을, 밭에 있어서는 약 100-500g : 20-120g : 20-140g의 혼합물을 사용하면 좋은 결과를 얻을 수 있다.S-benzyl thiol carbamate, phenoxy-compound and triazine-based compound of the active ingredient of the present invention is not to mention that the mixed dose is significantly reduced than when used in each step, the most preferred mixing range The ratio of S-benzylthiolcarbamate: phenoxy compound: triazine compound is 1: 0.01-0.3: 0.01-0.5 by weight ratio, and the amount of 10-argase varies depending on the field or crop condition to be controlled. If you use a mixture of 50-300g: 10-60g: 10-70g and about 100-500g: 20-120g: 20-140g in the field, you can get good results.

본 발명의 조성물은 논에서 사용할 경우, 입제(粒劑)로 제제(製劑)하는 것이 가장 효과적이다. 즉, 벤토나이트, 점토, 탈크, 석회석 등을 사용하여 증량하고 알킬벤젠설폰산나트륨, 폴리비닐 알코올, 리그닌 설폰산나트륨 등의 결합제를 가하여 물로 반죽하고, 압출조립한 다음 건조시키는 방법과, 디메틸포름아마이드 등의 적당한 용매에 녹이든가, 또는 녹이지 않고 입상규조토, 퍼어머클라이트 또는 벤토나이트, 탈크, 규조토, 점토, 석회석 등의 광물질 미분말, 알킬벤젠설폰산나트륨, 폴리비닐알코올, 리그닌설폰산나트륨 등의 결합제를 가하여 물로 반죽하고, 압출조립한 후 건조하고, 원하는 입도로 고르게 한 것에 균일하게 흡착시키는 방법 등을 사용하여 제조하고 입제를 손으로 또는 산립기

Figure kpo00002
나 헬리콥터 등을 사용하여 균일하게 산포하여 사용한다. 수화제일 때에는 규조토 등의 담체, 알킬 벤젠설폰산나트륨 등의 활성제를 배합하여 수화제를 제조하고, 물, 모래 등으로 희석하고 살포한다. 또, 유제일 때에는 톨루엔, 키실렌, 메틸나프탈렌, 알코올류, 시클로헥사논, DMF, DMSo 등의 용제, 폴리옥시에틸렌 등의 알킬아릴에테르, 디나프틸메탄 디설폰산칼슘 등의 활성제를 배합하여 유제를 제조하고, 물로 희석하여 살포한다. 물론, 필요하다면 다른 살충제, 살균제 또는 제초제와 혼합할 수도 있다.When the composition of the present invention is used in rice fields, it is most effective to formulate granules. That is, it is expanded using bentonite, clay, talc, limestone, and the like, added with a binder such as sodium alkylbenzenesulfonate, polyvinyl alcohol, sodium lignin sulfonate, kneaded with water, extruded and dried, and dimethylformamide Granular diatomaceous earth, permercite or mineral fine powders such as bentonite, talc, diatomaceous earth, clay, limestone, etc., dissolved or not dissolved in a suitable solvent, such as sodium alkylbenzenesulfonate, polyvinyl alcohol, sodium lignin sulfonate, etc. The binder is added, kneaded with water, extruded, dried, and evenly adsorbed to the desired particle size. The granulation is carried out by hand or granulator.
Figure kpo00002
Use it evenly by using a helicopter or the like. In the case of a wetting agent, a carrier such as diatomaceous earth and an activator such as sodium alkyl benzene sulfonate are blended to prepare a wetting agent, diluted with water, sand and the like and sprayed. In the case of an emulsion, an oil agent is prepared by blending an active agent such as toluene, xylene, methylnaphthalene, alcohols, solvents such as cyclohexanone, DMF, DMSo, alkylaryl ethers such as polyoxyethylene, and dinaphthylmethane disulfonate. Prepared, diluted with water and sprayed. Of course, it can also be mixed with other pesticides, fungicides or herbicides if necessary.

다음에 배합에 관하여 실시예를 들어 설명한다. 여기서, %는 중량 백분율을 나타낸다.Next, an Example is given and demonstrated about compounding. Where% represents weight percentage.

[실시예 1 : 입제]Example 1: granulation

BMC 5%, MCPP 아릴에스테르 1%, MES 1%, 리그닌 설폰산나트륨 2%, 화이트카아본 5%, 벤토나이트 86%를 균일하게 혼합분쇄하고, 물을 가하여 반죽하고 압출식조립기에서 조립한 다음, 건조시켜 14-32메시로 되게 정립하여 입제로 한다.BMC 5%, MCPP aryl ester 1%, MES 1%, sodium lignin sulfonate 2%, white carbon 5%, bentonite 86% was mixed and ground uniformly, kneaded with water and assembled in an extruder, It is dried, it is made into 14-32 mesh, and it is granulated.

[실시예 2 : 입제]Example 2: Granulation

CMES 5%, MCPB 에틸에스테르 0.8%, MIS 1.3%, 벤토나이트 48%, 점토 44.4%, 알킬벤젠설폰산나트륨 1%, 폴리비닐알코올 0.5%를 균일하게 혼합 분쇄하고, 물을 가하여 반죽하고 압출식 조립기로서 조립한 다음, 건조하고, 14-32메시로 되게 정립하여 입제로 한다.CMES 5%, MCPB ethyl ester 0.8%, MIS 1.3%, bentonite 48%, clay 44.4%, sodium alkylbenzenesulfonate 1%, polyvinyl alcohol 0.5% uniformly mixed and pulverized, kneaded with water and extruded granulator The granules were then granulated, dried, sieved to 14-32 mesh, and granulated.

[실시예 3 : 입제]Example 3: Granulation

MBIC 7%, 2,4-D-나트륨염 1.5%, MES 1%, 벤토나이트 40%, 점토 46%, 알킬벤젠설폰산나트륨 2%, 리그닌설폰산나트륨 2%를 균일하게 혼합분쇄하고, 물을 가하여 반죽하고 압출식 조립기로서 조립한 다음 건조하고, 14-32메시로 되게 정립하여 입제로 한다.MBIC 7%, 2,4-D-sodium salt 1.5%, MES 1%, bentonite 40%, clay 46%, alkylbenzenesulfonate 2%, sodium lignin sulfonate uniformly mixed and ground, It is added, kneaded, granulated as an extruded granulator, dried, and granulated to 14-32 mesh.

[실시예 4 : 입제]Example 4 granulation

BMC 7%, MCPB 1%, MES 2%, 중탄산칼슘 40%, 점토 46.5%, 알킬벤젠설폰산나트륨 1.5%, 리그닌설폰산나트륨 2%를 균일하게 혼합분쇄하고, 물을 가하여 반죽하고 압축식 조립기로서 조립한 다음, 건조하여, 14-32메시로 되게 정립하여 입제로 한다.BMC 7%, MCPB 1%, MES 2%, calcium bicarbonate 40%, clay 46.5%, sodium alkylbenzenesulfonate 1.5%, sodium lignin sulfonate 2% uniformly mixed, kneaded with water and kneaded The granules were then granulated, dried and sieved to 14-32 mesh to form granules.

[실시예 5 : 입제]Example 5 granulation

CBEC 7%, MCPP 아민염 1%, MIS 1.5%, 점토 40%, 알킬벤젠설폰산칼슘 1.5%, 벤토나이트 48.5%, 폴리비닐알코올 0.5%를 균일하게 혼합분쇄하여 물을 가하여 반죽하고 압출식 조립기로서 조립한 다음, 건조시켜, 14-32메시로 되게 정립하여 입제로 한다.CBEC 7%, MCPP amine salt 1%, MIS 1.5%, clay 40%, alkyl benzene sulfonate calcium 1.5%, bentonite 48.5%, polyvinyl alcohol 0.5%, mixed with a mixture of water and kneading, as an extruder granulator After granulation, it is dried, it is made to be 14-32 mesh, and it is granulated.

[실시예 6 : 입제]Example 6 granulation

MCPB 에틸에스테르를 5배량(중량비)의 DMF에 용해시킨 것 5%, MBIC 5% 및 MES 1%를 혼합용해하고, 이것을 8-32메시로서 사별(篩別)한 입상 규조토±90%에 균일하게 흡수시켜 입제로 한다.5% of MCPB ethyl ester dissolved in 5 times (weight ratio) DMF, 5% of MBIC, and 1% of MES were mixed and dissolved, and then uniformly dissolved into 8-32 mesh of granular diatomaceous earth ± 90%. Absorb it into granules.

[실시예 7 : 수화제]Example 7 Hydration

MBIC 40%, 2,4-D 에틸에스테르 10%, MIS 10%, 알킬벤젠설폰산나트륨 2%, 리그닌설폰산나트륨 2%, 화이트 카아본 10%, 규조토 26%를 균일하게 혼합분쇄하여 수화제로 한다.MBIC 40%, 2,4-D ethyl ester 10%, MIS 10%, sodium alkylbenzenesulfonate 2%, sodium lignin sulfonate 2%, white carbon 10%, diatomaceous earth 26%, and mixed with a hydrating agent do.

[실시예 8 : 유제]Example 8 Emulsion

CBEC 30%, MCPB 에틸에스테르 6%, MIS 10%, 키실렌 39%, 폴리옥시에틸렌 알킬아릴에테르 12%, 디나프틸메탄디설폰산칼슘 3%를 혼합 용해하여 유제로 한다.CBEC 30%, MCPB ethyl ester 6%, MIS 10%, xylene 39%, polyoxyethylene alkylaryl ether 12%, and calcium disnaphthyl methane disulfonate 3% are mixed and dissolved to obtain an emulsion.

[실시예 9 : 분제]Example 9 Powder

BMC 7%, MCPB 1%, MES 1.5% 및 규조토와 점토의 균등 혼합물 90.5%를 균일하게 혼합분쇄하여 분제로 한다. 다음에 실험예를 들어 구체적으로 본 발명의 효과를 설명한다.BMC 7%, MCPB 1%, MES 1.5%, and 90.5% of an even mixture of diatomaceous earth and clay are mixed and ground to obtain a powder. Next, the effects of the present invention will be described in detail with reference to experimental examples.

[실험예 (1) : 밭에 있어서의 발아전 토양처리 시험][Experimental Example (1): Soil Treatment Test Before Germination in Field]

800cm2의 폴리에틸렌제포트(Pot)에 밭토양(충적식양토(沖積殖壤土))를 충전하고, 각종 공시(供試) 잡초의 종자를 파종(금방동산이, 향무자는 괴경을 3cm의 깊이로 심는다)한 다음, 가볍게 복토진압(伏土鎭壓)을 하고, 실시예 7에 준하여 조제한 수화제를 물로 소정농도로 희석하고, 10아아르당 100ℓ의 비율로 분무처리하였다. 처리한 다음 온실 안에 두고 포트를 항상 바의 상태로 유지하고, 처리 30일 후에 관찰에 의하여 조사하였다. 결과를 제1표에 표시한다.Fill a 800 cm 2 polyethylene pot with a field soil (Alluvial Soil), and sow seeds of various publicly available weeds. Then, the soil was subjected to light earthquake suppression, and the hydrating agent prepared according to Example 7 was diluted with water to a predetermined concentration, and sprayed at a rate of 100 liters per 10 liters. After treatment, they were placed in a greenhouse and the pot was always kept in the state of a bar and examined by observation 30 days after the treatment. The results are shown in the first table.

단, 표중 5는 완전고사, 4는 80% 이상의 살초력을 나타냄.However, 5 in the table is a complete test, 4 is more than 80% killing power.

3은 50-80%의 살초력을 나타냄.3 shows 50-80% killing power.

2는 20-50%의 살초력을 나타냄.2 represents 20-50% killing power.

1은 20% 이하의 살초력을 나타냄.1 indicates less than 20% killing power.

0은 효과 없음을 나타낸 것이다.0 indicates no effect.

[제1표][Table 1]

Figure kpo00003
Figure kpo00003

Figure kpo00004
Figure kpo00004

Figure kpo00005
Figure kpo00005

Figure kpo00006
Figure kpo00006

[실험에 (2) : 채소밭에 있어서의 제초시험][Experiment (2): Herbicide test in vegetable garden]

채소밭을 5월 20일에 갈고 일으켜서 정지 1구당 4m2로 구획하고, 2연제(連制)로 하여 실시하였다.The vegetable garden was plowed and raised on May 20, and divided into 4 m 2 per stop, and it was implemented as a double flame retardant.

그후, 공시작물을 2-3cm의 길이로 파종하고, 즉시 실시예 7에 준하여 조제한 수화제를 물로서 소정농도로 희석하고, 10이아르당 100ml의 비율로 약제를 처리하였다.Thereafter, the starting material was seeded to a length of 2-3 cm, and the hydrous prepared immediately according to Example 7 was diluted with water to a predetermined concentration, and the drug was treated at a rate of 100 ml per 10 parts.

조사는 6월 20일에 관찰에 의하여 실험예 1의 효과표시에 따라서 조사하였다.The investigation was carried out according to the indication of the effect of Experimental Example 1 by observation on June 20.

결과를 제2표에 표시한다.The results are shown in the second table.

[제2표][Table 2]

Figure kpo00007
Figure kpo00007

[실험예 (3) : 이식논에 있어서의 제초시험]Experimental Example (3): Herbicide Test in Transplanted Rice Fields

논에 벼묘(품종 : 금납품)을 6월 10일에 이식하고, 이 논을 1구 5m2으로 구획하고 1약제(藥劑) 2연제(連制)로 하여 담수 상태에서 시험을 행하였다. 이식 후, 6월 25일에 실시예 3에 준하여 조제한 입제의 소정약량을 처리하고, 처리 후 7월 25일에 제초효과를 조사하였다. 결과의 시험예(1)의 표시에 따라, 제3표에 표시한다.Rice seedlings were harvested on June 10, and the rice paddies were divided into 1 piece 5m 2 and tested in fresh water with 1 drug diuretic. After transplantation, the prescribed dose of granules prepared according to Example 3 was treated on June 25, and the herbicidal effect was investigated on July 25 after the treatment. According to the display of the test example (1) of the result, it displays in a 3rd table | surface.

[제3표][Table 3]

Figure kpo00008
Figure kpo00008

Figure kpo00009
Figure kpo00009

Figure kpo00010
Figure kpo00010

[실험예 (4) : 엽령이 진행된 올챙이 고랭이에 대한 효과][Experimental Example (4): Effect on the tadpoles of the tadpole advanced

올챙이 고랭이가 우선적으로 발생하는 논에 벼모(품종 : 금납품)를 6월 11일에 이식하고, 이 논을 1구당 5m2로 구획하여, 1약제 2연제, 담수상태에서 시험을 행하였다. 이식 후 6월 26일에 실시예에 준하여 조사한 입제의 소정량을 처리하고, 처리 후 7월 26일에 제초효과를 조사하였다. 결과에 대한 표시는 실험에 1의 표시에 따르고, 결과를 제4표에 표시한다.Rice seedlings were harvested on June 11 in paddy fields where tadpoles had higher priority, and the rice paddies were divided into 5 m 2 per plot and tested in two-drug, fresh water. After transplantation, a predetermined amount of granules irradiated in accordance with Examples was treated on June 26, and the herbicidal effect was examined on July 26 after treatment. The indication of the result follows the indication of 1 in the experiment, and the result is shown in the fourth table.

[제4표][Table 4]

Figure kpo00011
Figure kpo00011

[실험에 (5) : 늦처리에 의한 올미방제시험][Experiment (5): Lame control test by late treatment]

올미가 많이 발생하는 논을 선택하고, 써레질 정지후 6월 5일에 3엽기의 논의 활달한 모를 기계적으로 이식하였다. 이식후 논을 1구 5m2로 구획하고, 1약제 2연제로서 입제를 담수처리하였다. 처리는 이식 22일후인 6월 27일에 행하고, 약제는 각구 함께 실시예에 준하여 입제로 제제하여, 소정량을 투입하였다.The rice field, which has a high number of snares, was selected, and mechanically transplanted the three-leaf ricefield active hairs on June 5 after harrowing was stopped. After transplanting, the rice paddies were partitioned into 1 sphere 5m 2 , and the granules were treated with fresh water as a single drug retardant. The treatment was carried out on June 27, 22 days after transplantation, and the drug was prepared in granules according to the examples together with each mouth, and a predetermined amount was added thereto.

처리시의 올미는 6-7엽기에 달하고 있었다. 제초효과는 처리 40일 후인 9월 6일에 각 시험구의 중심부 50×50cm 안의 올미를 뽑아내어 100℃로 건조하여 잔초량(殘草量)으로서 비교하였다.The snare at the time of treatment reached 6-7 leaf stage. The herbicidal effect was compared to the remaining amount of the herb after extracting a snare in 50 × 50 cm of the center of each test zone on September 6, 40 days after the treatment.

결과를 제5표에 표시함.The results are shown in Table 5.

[제5표][Table 5]

Figure kpo00012
Figure kpo00012

Claims (1)

하기 일반식(I)의 S-벤질-N,N-디알킬티올 카르바메이트와 하기 일반식(II)의 페녹시계 화합물이나 그의 염 및 2-메틸티오-4,6-비스알킬아미노-S-트리아진 화합물을 1 : 0.01~0.3 : 0.01~0.5의 비율로 조성한 제초제 조성물.S-benzyl-N, N-dialkylthiol carbamate of the following general formula (I), a phenoxy compound of the following general formula (II), a salt thereof and 2-methylthio-4,6-bisalkylamino-S -The herbicide composition which comprised the triazine compound in the ratio of 1: 0.01-0.3: 0.01-0.5.
Figure kpo00013
Figure kpo00013
상기 식에서, R는 알킬기, R′는 알킬렌기, X는 할로겐원자 또는 메틸기, X′는 염소원자 또는 메틸기임.Wherein R is an alkyl group, R 'is an alkylene group, X is a halogen atom or a methyl group, X' is a chlorine atom or a methyl group.
KR7401084A 1974-01-01 1974-01-01 Herbicidal composition KR800000648B1 (en)

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