JPH09175914A - Herbicide composition - Google Patents
Herbicide compositionInfo
- Publication number
- JPH09175914A JPH09175914A JP35242995A JP35242995A JPH09175914A JP H09175914 A JPH09175914 A JP H09175914A JP 35242995 A JP35242995 A JP 35242995A JP 35242995 A JP35242995 A JP 35242995A JP H09175914 A JPH09175914 A JP H09175914A
- Authority
- JP
- Japan
- Prior art keywords
- chemical formula
- effect
- parts
- rice
- chemical
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 37
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 26
- 239000004009 herbicide Substances 0.000 title abstract description 10
- -1 phenyl-N-methylcarbamate compound Chemical class 0.000 claims abstract description 18
- ICWUMLXQKFTJMH-UHFFFAOYSA-N Etobenzanid Chemical compound C1=CC(OCOCC)=CC=C1C(=O)NC1=CC=CC(Cl)=C1Cl ICWUMLXQKFTJMH-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000004480 active ingredient Substances 0.000 claims abstract description 3
- 239000002689 soil Substances 0.000 abstract description 17
- 239000003795 chemical substances by application Substances 0.000 abstract description 16
- 230000000694 effects Effects 0.000 abstract description 12
- 241001148683 Zostera marina Species 0.000 abstract description 7
- 230000002195 synergetic effect Effects 0.000 abstract description 5
- 239000003814 drug Substances 0.000 abstract description 4
- 229940079593 drug Drugs 0.000 abstract description 4
- 230000003247 decreasing effect Effects 0.000 abstract 1
- 239000000126 substance Substances 0.000 description 64
- 241000209094 Oryza Species 0.000 description 29
- 235000007164 Oryza sativa Nutrition 0.000 description 28
- 235000009566 rice Nutrition 0.000 description 28
- 238000009472 formulation Methods 0.000 description 20
- 238000012360 testing method Methods 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 8
- 241000196324 Embryophyta Species 0.000 description 7
- 238000010899 nucleation Methods 0.000 description 7
- 239000008187 granular material Substances 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229910001868 water Inorganic materials 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000003359 percent control normalization Methods 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 239000004563 wettable powder Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 231100000674 Phytotoxicity Toxicity 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 238000012364 cultivation method Methods 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- YWQRFDUUFJNRMN-UHFFFAOYSA-N (2-butan-2-ylphenyl)-methylcarbamic acid Chemical compound CCC(C)C1=CC=CC=C1N(C)C(O)=O YWQRFDUUFJNRMN-UHFFFAOYSA-N 0.000 description 1
- 241001414720 Cicadellidae Species 0.000 description 1
- 241001466042 Fulgoromorpha Species 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- CVQODEWAPZVVBU-UHFFFAOYSA-N XMC Chemical compound CNC(=O)OC1=CC(C)=CC(C)=C1 CVQODEWAPZVVBU-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000008378 aryl ethers Chemical class 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- GTCAXTIRRLKXRU-UHFFFAOYSA-N carbamic acid methyl ester Natural products COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 description 1
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- QBSJMKIUCUGGNG-UHFFFAOYSA-N isoprocarb Chemical compound CNC(=O)OC1=CC=CC=C1C(C)C QBSJMKIUCUGGNG-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- RLEPUHXXMVRJDI-UHFFFAOYSA-N naphthalen-2-yl n-methylcarbamate Chemical compound C1=CC=CC2=CC(OC(=O)NC)=CC=C21 RLEPUHXXMVRJDI-UHFFFAOYSA-N 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- 238000009333 weeding Methods 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
(57)【要約】
【構成】2’,3’−ジクロロ−4−エトキシメトキシ
ベンズアニリドと、フェニル−N−メチルカーバメート
化合物を有効成分として含有することを特徴とする除草
剤組成物。
【効果】本発明の除草剤組成物は、イネ科雑草に対し土
壌残効期間の延長効果が観察され、また相乗効果を発揮
するため薬剤の投下薬量を減ずることが可能となり、さ
らに、個々の薬剤が有する作物選択性を減じることな
く、イネ科雑草を長期間にわたり完全に防除することが
できる。(57) [Summary] [Structure] A herbicide composition comprising 2 ', 3'-dichloro-4-ethoxymethoxybenzanilide and a phenyl-N-methylcarbamate compound as active ingredients. [Effect] The herbicidal composition of the present invention has an effect of prolonging the soil residual effect period on grass weeds, and since it exerts a synergistic effect, it is possible to reduce the amount of the drug to be dropped. It is possible to completely control grass weeds for a long period of time without decreasing the crop selectivity possessed by these agents.
Description
【0001】[0001]
【発明の属する技術分野】本発明は、除草剤組成物に関
するものである。TECHNICAL FIELD The present invention relates to a herbicide composition.
【0002】[0002]
【従来の技術】現在のイネ栽培地において防除対象にな
る雑草の種類は非常に多いが、特に問題となるものとし
て、1年生イネ科雑草のノビエと1年生広葉雑草があげ
られる。その中でも、イネ科雑草はイネ科作物と近縁種
であるため選択的防除が難しく、しかも発生量も多いた
め、イネ科雑草が残草すると農耕地では作物の減収問題
に直結してしまう。そのため現在の防除方法は、移植イ
ネを移植し雑草の発生前に土壌処理除草剤を処理するこ
とにより、ノビエおよび1年生広葉雑草の防除を行って
いるが、除草効果の持続時間は35〜45日ほどであ
る。2. Description of the Related Art There are many kinds of weeds to be controlled in the present rice cultivating land, and the particularly problematic ones are the annual grass weed Novie and annual broadleaf weed. Among them, grass weeds are closely related to gramineae crops, so that selective control is difficult, and the amount of grass weeds is large. If grass weeds are left over, it will directly lead to the problem of crop loss in agricultural fields. Therefore, the current control method is to control Nobie and annual broad-leaved weeds by transplanting transplanted rice and treating with a soil treatment herbicide before the emergence of weeds, but the duration of the herbicidal effect is 35 to 45. It's about a day.
【0003】本発明の組成物である2’,3’−ジクロ
ロ−4−エトキシメトキシベンズアニリド(以下、化1
と称す)は、既知化合物であり、水稲用除草剤として知
られている(特開昭56−73055)。The composition of the present invention, 2 ', 3'-dichloro-4-ethoxymethoxybenzanilide (hereinafter
Is a known compound and is known as a herbicide for paddy rice (JP-A-56-73055).
【0004】本発明の一方の組成物であるフェニル−N
−メチルカーバメート化合物には、1−ナフチル−N−
メチルカーバメート(以下、化2と称す)、2−ナフチ
ル−N−メチルカーバメート(以下、化3と称す)、
3,5−キシリル−N−メチルカーバメート(以下、化
4と称す)、2−セコンドリーブチルフェニル−N−メ
チルカーバメート(以下、化5と称す)、メタトリル−
N−メチルカーバメート(以下、化6と称す)および2
−イソプロピルフェニル−N−メチルカーバメート(以
下、化7と称す)などがあり、水稲用殺虫剤として広く
用いられている。フェニル−N−メチルカーバメート化
合物は、通常使用薬量では、茎葉散布剤として殺虫効果
を発揮し、ウンカ類およびヨコバイ類防除剤として知ら
れている。One composition of the present invention, Phenyl-N.
-Methylcarbamate compounds include 1-naphthyl-N-
Methyl carbamate (hereinafter referred to as Chemical formula 2), 2-naphthyl-N-methyl carbamate (hereinafter referred to as Chemical formula 3),
3,5-xylyl-N-methylcarbamate (hereinafter referred to as "Chemical formula 4"), 2-secondary butylphenyl-N-methylcarbamate (hereinafter referred to as "Chemical formula 5"), methatril-
N-methyl carbamate (hereinafter referred to as "Chemical formula 6") and 2
-Isopropylphenyl-N-methylcarbamate (hereinafter referred to as "Chemical formula 7") and the like, which are widely used as insecticides for paddy rice. The phenyl-N-methylcarbamate compound exerts an insecticidal effect as a foliar spraying agent in a normally used dose, and is known as a control agent for planthoppers and leafhoppers.
【0005】[0005]
【発明が解決しようとする課題】移植イネの移植後、雑
草が結実しないために必要な除草効果持続期間は、45
日程度とされている。化1は、ノビエと移植イネとの間
に高度の作物選択性を有するが、土壌処理後、除草剤と
しての除草効果の持続期間は30〜40日程度であり、
さらなる除草効果の持続期間が要望されている。Problems to be Solved by the Invention After transplanting rice, the weeding effect duration required for the weeds not to bear fruit is 45
It is said to be about a day. Chemical formula 1 has a high degree of crop selectivity between Nobie and transplanted rice, but the duration of the herbicidal effect as a herbicide is about 30 to 40 days after soil treatment,
Further duration of herbicidal effect is required.
【0006】さらに、現在のイネ栽培においては、労働
力の減少のために移植水稲栽培法に代わり直播水稲栽培
法の普及が切望されている。しかし、直播水稲栽培にお
いては、除草剤が直播イネに対し薬害を生じ初期生育が
遅れる等の問題があり、優れた選択性を有する除草剤の
出現が望まれている。化1は、移植イネと同様、直播イ
ネとノビエとの間に高い作物選択性を有するが、土壌処
理後の除草効果持続期間は30〜40日程度である。直
播水稲栽培において、雑草が結実しないために必要な持
続期間は約60日とされており、より長い除草効果の持
続期間が希求されている。Further, in the current rice cultivation, there is a strong demand for the spread of the direct seeding rice cultivation method instead of the transplanted rice cultivation method in order to reduce the labor force. However, in the direct seeding paddy rice cultivation, there is a problem that the herbicide causes phytotoxicity to the direct seeding rice and the initial growth is delayed, and thus the emergence of a herbicide having excellent selectivity is desired. Similar to the transplanted rice, the chemical formula 1 has a high crop selectivity between the direct-seeded rice and the Nobye, but the herbicidal effect duration after soil treatment is about 30 to 40 days. In direct seeding paddy rice cultivation, the duration required for the weeds not to set fruit is about 60 days, and a longer duration of herbicidal effect is desired.
【0007】[0007]
【課題を解決するための手段】本発明者らは、これらの
問題点を解決するために、様々な組成を検討した結果、
本発明の化1とフェニル−N−メチルカーバメート化合
物を混合することにより、化1の土壌残効期間が延長
し、さらに、化1単用の除草効果をはるかに超えた相乗
効果を示すことを見いだした。The present inventors have studied various compositions in order to solve these problems, and as a result,
By mixing the chemical formula 1 of the present invention with the phenyl-N-methylcarbamate compound, the soil residual effect period of the chemical formula 1 is prolonged, and further, a synergistic effect far exceeding the herbicidal effect of the chemical formula 1 alone is shown. I found it.
【0008】さらに、本効果が実際に利用価値があるか
否かを確認するために、投下薬量、混合比、作用範囲、
効果、あるいは作物に対する薬害などに関し、詳細な検
討を加え本発明を完成した。Further, in order to confirm whether or not the present effect is actually useful, the amount of the dropped drug, the mixing ratio, the range of action,
The present invention has been completed by making detailed examinations regarding the effects or the chemical damage to crops.
【0009】本発明における相乗効果は、1年生イネ科
雑草のノビエに対し、低薬量から高薬量まで広い範囲で
認められた。一方、イネに対する薬害は移植イネおよび
直播栽培イネに対し相乗的に増加するようなことはな
く、イネとノビエとの高い選択性は維持された。The synergistic effect of the present invention was observed in a wide range from low dose to high dose against Nobie, an annual grass weed. On the other hand, the phytotoxicity against rice did not increase synergistically with transplanted rice and direct-seeded rice, and the high selectivity between rice and novier was maintained.
【0010】これによって、自然条件下の圃場におい
て、化1の高い選択作用性を維持したまま、相乗効果的
な除草効果が発揮され、その土壌残効期間も延長される
ことから、本発明の除草剤組成物はきわめて実用価値が
高いことが確認された。As a result, in a field under natural conditions, a synergistic herbicidal effect is exerted while maintaining the high selective action of the chemical formula 1, and the soil residual effect period is extended. It was confirmed that the herbicide composition has extremely high practical value.
【0011】[0011]
【発明の実施の形態】本発明の実際上の使用量は有効成
分として化1が10g〜200g/10a、好ましくは
25g〜150g/10aがよい。フェニル−N−メチ
ルカーバメート化合物は、1g〜200g/10a、好
ましくは10g〜100g/10aがよい。ただし、化
1とフェニル−N−メチルカーバメート化合物との合計
の薬量は100g〜200g/10aが好ましい。BEST MODE FOR CARRYING OUT THE INVENTION In the practical use amount of the present invention, 10 g to 200 g / 10a, preferably 25 g to 150 g / 10a of the chemical formula 1 is used as an active ingredient. The phenyl-N-methyl carbamate compound may be 1 g to 200 g / 10a, preferably 10 g to 100 g / 10a. However, the total dose of Chemical Formula 1 and the phenyl-N-methylcarbamate compound is preferably 100 g to 200 g / 10a.
【0012】本発明の化1とフェニル−N−メチルカー
バメート化合物との併用割合は、本発明の優れた選択性
を実質的に損なわない範囲内で経済性を考慮し、適宜に
選択することができる。例えば、化1:フェニル−N−
メチルカーバメート化合物=0.1:1〜10:1(重
量比)の併用割合を例示できる。好ましくは、化1:フ
ェニル−N−メチルカーバメート化合物=1:1〜5:
1(重量比)の併用割合を例示できる。The combination ratio of the compound of the present invention 1 and the phenyl-N-methyl carbamate compound may be appropriately selected in consideration of economical efficiency within a range that does not substantially impair the excellent selectivity of the present invention. it can. For example, chemical formula 1: phenyl-N-
A combination ratio of methyl carbamate compound = 0.1: 1 to 10: 1 (weight ratio) can be exemplified. Preferably, the chemical formula 1: phenyl-N-methyl carbamate compound = 1: 1 to 5:
A combination ratio of 1 (weight ratio) can be exemplified.
【0013】本発明化合物を散布するにあたっては、例
として一体製剤による散布が挙げられる。一体製剤の場
合、均一に散布する製剤型、例えば粒剤、水和剤、顆粒
水和剤およびゾル剤が挙げられる。In spraying the compound of the present invention, for example, spraying by an integral preparation can be mentioned. In the case of a monolithic preparation, it includes a dosage form that is uniformly dispersed, such as granules, wettable powders, wettable granules and sol preparations.
【0014】組成物に使用するキャリア−としては、不
活性な無機物、例えば、水、ベントナイト、ゼオライ
ト、炭カル、食塩などを使用することができる。As the carrier used in the composition, an inert inorganic substance such as water, bentonite, zeolite, calcium carbonate, or salt can be used.
【0015】分散剤、あるいは固着剤としては、各種の
界面活性剤、例えば、アルキルナフタレンスルホン酸ホ
ルマリン縮合物、ジアルキルスルホサクシネート、ポリ
オキシエチレンアルキルアリールエーテル、ポリオキシ
エチレンラウリルエーテル、ポリオキシエチレンアルキ
ルアリールエーテル、ポリオキシエチレンドデシルエー
テルなどが挙げられる。As the dispersant or the fixing agent, various surfactants such as alkylnaphthalenesulfonic acid formalin condensate, dialkylsulfosuccinate, polyoxyethylene alkylaryl ether, polyoxyethylene lauryl ether, polyoxyethylene alkyl are used. Examples include aryl ethers and polyoxyethylene dodecyl ethers.
【0016】また、増粘剤、消泡剤、安定剤などの補助
剤を適宜選択の上添加することもできる。Further, auxiliary agents such as a thickener, a defoaming agent and a stabilizer can be appropriately selected and added.
【0017】[0017]
【実施例】以下、実施例をもって本発明を具体的に説明
する。実施例は、〔製剤例〕と〔試験例〕とに分けて記
述した。The present invention will be specifically described below with reference to examples. The examples are described separately as [formulation example] and [test example].
【0018】以下、本発明の組成物を製剤別に製剤例と
して具体的に示す。The compositions of the present invention will be specifically shown below as formulation examples for each formulation.
【0019】〔製剤例1〕 水和剤の作成 (化1の単
剤) 化1の50部(部は、いずれも重量部を示す。以下、同
じ)にクレー33部、ホワイトカーボン1部を加えジェ
ットミルで粉砕後、さらにクレー9部とホワイトカーボ
ン1部を加え均一に混合し、粉末界面活性剤のソルポー
ル5039(東邦化学工業(株)商標)5部とラピゾー
ルBB75(日本油脂(株)商標)1部を加えよく混合
し、化1の50%を含有する水和剤を得た。[Formulation Example 1] Preparation of wettable powder (single agent of Chemical Formula 1) 50 parts of Chemical Formula 1 (parts represent parts by weight; hereinafter the same) 33 parts of clay and 1 part of white carbon After crushing with a jet mill, 9 parts of clay and 1 part of white carbon were further added and mixed uniformly, and 5 parts of powdered surfactant Solpol 5039 (trademark of Toho Chemical Industry Co., Ltd.) and Lapizole BB75 (NOF CORPORATION). 1 part (trademark) was added and mixed well to obtain a wettable powder containing 50% of Chemical Formula 1.
【0020】〔製剤例2〕 粒剤の作成 (化1と化2
の混合剤) 化1の10部と化2の5部にクレー45部、ベントナイ
ト20部を加え均一に混合し、界面活性剤のソルポール
800A(東邦化学工業(株)商標)10部およびトリ
ポリリン酸ソーダ10部を加え、さらに適当量の水を加
え混練し、造粒機を用い造粒し、化1の10%と化2の
5%を含有する粒剤を得た。[Formulation Example 2] Preparation of Granules (Chemical Formula 1 and Chemical Formula 2)
Mixing agent) 10 parts of Chemical Formula 1 and 5 parts of Chemical Formula 2 were mixed with 45 parts of clay and 20 parts of bentonite and mixed uniformly, and 10 parts of surfactant Solpol 800A (trademark of Toho Chemical Industry Co., Ltd.) and tripolyphosphoric acid. 10 parts of soda was added, an appropriate amount of water was further added and kneaded, and the mixture was granulated using a granulator to obtain granules containing 10% of chemical formula 1 and 5% of chemical formula 2.
【0021】〔製剤例3〕 顆粒水和剤の作成 (化1
と化3の混合剤) 化1の60部に対し、化3の20部、ホワイトカーボン
5部、ソルポール5039(東邦化学工業(株)商標)
4部、バンノックスPW(日本乳化剤(株)商標)1部
およびトリポリリン酸ソーダ10部を加え、さらに水1
0部を加えて押し出し造粒機にて造粒し、乾燥して水分
を除いた後にふるい分けして、10〜48メッシュの化
1の60%と化3の20%を含有する顆粒水和剤を得
た。[Formulation Example 3] Preparation of granule wettable powder
And a mixture of Chemical Formula 3) 60 parts of Chemical Formula 1, 20 parts of Chemical Formula 3, 5 parts of white carbon, Solpol 5039 (trademark of Toho Chemical Industry Co., Ltd.)
4 parts, 1 part of Vannox PW (trademark of Nippon Emulsifier Co., Ltd.) and 10 parts of sodium tripolyphosphate were added, and further 1 part of water was added.
Granule wettable powder containing 0% and granulated by an extrusion granulator, dried to remove water and then sieved to contain 60% of Chemical Formula 1 and 20% of Chemical Formula 3 of 10-48 mesh Got
【0022】〔製剤例4〕 ゾル剤の作成 (化1と化
4の混合剤) 化1の30部、化4の10部に水48.3部と界面活性
剤のソルポール3742(東邦化学工業(株)商標)7
部と消泡剤としてソルポール5712(東邦化学工業
(株)商標)0.5部を加えて、サンドグラインダーで
粉砕し、取り出し後に、安定剤としてエチレングリコー
ル4部とVANGEL−B(三洋化成(株)商標)0.
2部を加え、良く攪拌して、化1の30%と化4の10
%を含有するゾル剤を得た。[Formulation Example 4] Preparation of sol agent (mixture of chemical formula 1 and chemical formula 4) 30 parts of chemical formula 1 and 10 parts of chemical formula 4 in 48.3 parts of water and surfactant Solpol 3742 (Toho Chemical Industry Co., Ltd.) Trademark Co., Ltd. 7
Parts and 0.5 parts of Solpol 5712 (trademark of Toho Chemical Industry Co., Ltd.) as an antifoaming agent, crushed with a sand grinder, and after taking out, 4 parts of ethylene glycol as a stabilizer and VANGEL-B (Sanyo Chemical Co., Ltd. ) Trademark) 0.
Add 2 parts and stir well to give 30% of Chemical formula 1 and 10 of Chemical formula 4
% Of the sol was obtained.
【0023】以下、本発明の除草剤の除草効果について
試験例をもって具体的に示す。Hereinafter, the herbicidal effect of the herbicide of the present invention will be specifically described with reference to test examples.
【0024】〔試験例1〕 温室内土壌残効試験 200cm2のポリプロピレン製ポットに水田土壌を充
填し、湛水深3cmとした。翌日、製剤例1に準じた処
方で製剤した化1、化2および化3の単剤および混合剤
の所定量と、製剤例4に準じた処方で製剤した化1、化
4、化5、化6および化7の単剤および混合剤の所定量
とを土壌表面に均一散布した。薬剤処理1週間毎にノビ
エ種子を20粒づつ土壌表面に播種し、ノビエ種子播種
2週間後に観察による調査を行なった。結果は、表1に
示す。Test Example 1 Soil residual effect test in greenhouse A 200 cm 2 polypropylene pot was filled with paddy soil to make a submerged depth of 3 cm. The following day, the prescribed amounts of the single agents and the mixed agents of Chemical Formula 1, Chemical Formula 2 and Chemical Formulation 3 formulated with the formulation according to Formulation Example 1 and Chemical Formula 1, Chemical Formulation 4 and Chemical Formulation 5 with the formulation according to Formulation Example 4; The single agents of Chemical formulas 6 and 7 and a predetermined amount of the mixed agent were uniformly sprayed on the soil surface. 20 seeds of Novier seeds were sown on the soil surface every 1 week of the chemical treatment, and two weeks after the seeding of the Novier seeds, an observational investigation was conducted. The results are shown in Table 1.
【0025】観察調査の結果は、次の評価基準で表示し
た。(以下の調査も同じ。) 〔除草効果の評価基準〕 0:無処理同様 1:20%防除 2:40%防除 3:60%防除 4:80%防除 5:完全防除The results of the observational survey are displayed according to the following evaluation criteria. (The same applies to the following surveys.) [Evaluation criteria for herbicidal effect] 0: Same as no treatment 1: 20% control 2: 40% control 3: 60% control 4: 80% control 5: Complete control
【0026】[0026]
【表1】 [Table 1]
【0027】〔試験例2〕 温室内除草効果試験 200cm2のポリプロピレン製ポットに水田土壌を充
填し、ノビエを土壌表面に播種し、催芽したイネを土壌
表面に植付、2〜2.5葉期に生育した水稲を移植し、
湛水条件とした。湛水深は、3cmとした。処理は、製
剤例1に準じた処方で製剤した化1、化2および化3の
単剤および混合剤の所定量と、製剤例4に準じた処方で
製剤した化1、化4、化5、化6および化7の単剤およ
び混合剤の所定量とを土壌表面に均一散布した。散布1
カ月後に観察による調査を行った。結果は、表2に示
す。Test Example 2 Herbicidal Effect Test in Greenhouse A 200 cm 2 polypropylene pot was filled with paddy soil, seeds of Nobie were sown on the soil surface, and the germinated rice was planted on the soil surface to obtain 2 to 2.5 leaves. Transplanted paddy rice grown in the
Flooding conditions were used. The water depth was 3 cm. The treatments were the prescribed amounts of the single agents and the mixed agents of Chemical Formula 1, Chemical Formula 2 and Chemical Formula 3 formulated with the formulation according to Formulation Example 1, and Chemical Formula 1, Chemical Formula 4 and Chemical Formula 5 with the formulation according to Formulation Example 4. , A predetermined amount of the single agent of Chemical formula 6 and Chemical agent 7 and a predetermined amount of the mixed agent were uniformly sprayed on the soil surface. Scatter 1
An observational study was conducted a month later. The results are shown in Table 2.
【0028】[0028]
【表2】 [Table 2]
【0029】[0029]
【表3】 [Table 3]
【0030】[0030]
【表4】 [Table 4]
【0031】[0031]
【表5】 [Table 5]
【0032】[0032]
【表6】 [Table 6]
【0033】[0033]
【表7】 [Table 7]
【0034】〔試験例3〕 圃場テスト 2m2の単位区を設け、ノビエの種子を土壌表面に播種
した。移植水稲は、2葉期に生育した水稲を3本1株と
し10株移植した。直播水稲は、催芽したイネを土壌表
面に植付けた。なお湛水深は3cmとした。水稲移植5
日後(雑草発生始期)および18日後(ノビエ3葉期)
に、製剤例に準じた処方で製剤した化1の単剤および一
体製剤の所定量を区内に均一に散布した。散布1カ月後
に観察による調査を行った。調査の基準は、試験例1に
準じた。結果は、表3に示す。[Test Example 3] Field test A unit of 2 m 2 was provided, and seeds of Novier were sown on the soil surface. As the transplanted paddy rice, 10 paddy rice plants grown in the 2nd leaf stage were transplanted in 3 strains. For direct-seeded paddy rice, germinated rice was planted on the soil surface. The submersion depth was 3 cm. Rice transplant 5
Day later (the beginning of weed development) and 18 days later (Novier 3 leaf stage)
Then, a predetermined amount of the single agent of Formula 1 and the integrated preparation, which were prepared by the formulation according to the formulation example, were uniformly dispersed in the plot. One month after the application, a survey by observation was conducted. The criteria for investigation were in accordance with Test Example 1. The results are shown in Table 3.
【0035】[0035]
【表8】 [Table 8]
【0036】[0036]
【表9】 [Table 9]
【0037】[0037]
【発明の効果】各試験例から明らかなように、本発明の
除草剤組成物は、(1)化1とフェニル−N−メチルカ
ーバメート化合物を混合することにより、土壌残効期間
の延長効果が発現し、移植水稲栽培や直播水稲栽培で必
要とされる60日まで化1の除草効果持続期間を長くす
ることが可能となる。As is apparent from each test example, the herbicidal composition of the present invention has the effect of extending the soil residual effect period by mixing (1) Chemical formula 1 and the phenyl-N-methylcarbamate compound. It is possible to prolong the duration of the herbicidal effect of Chemical 1 up to 60 days, which is required for transplanted paddy rice cultivation and direct seeding paddy rice cultivation.
【0038】(2)化1とフェニル−N−メチルカーバ
メート化合物を混合することにより相乗効果が発現し、
化1単剤での投下薬量に比べ、化1の投下薬量を減ずる
ことが可能となる。(2) A synergistic effect is exhibited by mixing the compound 1 and the phenyl-N-methylcarbamate compound,
It is possible to reduce the amount of the drug administered by Chemical 1 as compared with the amount of the drug administered by Chemical 1 alone.
【0039】また、(3)化1とフェニル−N−メチル
カーバメート化合物を混合することにより、化1に示す
化合物が有する作物選択性を保持したまま、ノビエを完
全に防除することが可能となる。Further, by mixing (3) Chemical formula 1 with a phenyl-N-methylcarbamate compound, it is possible to completely control Nobies while maintaining the crop selectivity of the compound shown in Chemical formula 1. .
【0040】以上の効果より、本発明の除草剤組成物
は、移植水稲栽培においても、直播水稲栽培において
も、きわめて有用な土壌処理除草剤組成物である。From the above effects, the herbicidal composition of the present invention is a very useful soil-treating herbicidal composition for both transplanted rice cultivation and direct seeding rice cultivation.
Claims (1)
キシベンズアニリドと、フェニル−N−メチルカーバメ
ート化合物を有効成分として含有することを特徴とする
除草剤組成物。1. A herbicidal composition comprising 2 ', 3'-dichloro-4-ethoxymethoxybenzanilide and a phenyl-N-methylcarbamate compound as active ingredients.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP35242995A JPH09175914A (en) | 1995-12-28 | 1995-12-28 | Herbicide composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP35242995A JPH09175914A (en) | 1995-12-28 | 1995-12-28 | Herbicide composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH09175914A true JPH09175914A (en) | 1997-07-08 |
Family
ID=18424022
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP35242995A Pending JPH09175914A (en) | 1995-12-28 | 1995-12-28 | Herbicide composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH09175914A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011195492A (en) * | 2010-03-19 | 2011-10-06 | Hodogaya Chem Co Ltd | Method for controlling digitaria ciliaris developing in western turf |
-
1995
- 1995-12-28 JP JP35242995A patent/JPH09175914A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011195492A (en) * | 2010-03-19 | 2011-10-06 | Hodogaya Chem Co Ltd | Method for controlling digitaria ciliaris developing in western turf |
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