CN106922715A - A kind of Herbicidal combinations of Sulfometuron Methyl containing promazine with ethobenzanid and its application - Google Patents
A kind of Herbicidal combinations of Sulfometuron Methyl containing promazine with ethobenzanid and its application Download PDFInfo
- Publication number
- CN106922715A CN106922715A CN201710133335.4A CN201710133335A CN106922715A CN 106922715 A CN106922715 A CN 106922715A CN 201710133335 A CN201710133335 A CN 201710133335A CN 106922715 A CN106922715 A CN 106922715A
- Authority
- CN
- China
- Prior art keywords
- herbicidal combinations
- promazine
- ethoxyfen
- ethobenzanid
- methyl
- 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
Classifications
-
- 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<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
本发明公开了一种含丙嗪嘧磺隆与乙氧苯草胺的除草组合物,该除草组合物以丙嗪嘧磺隆与乙氧苯草胺为主要有效成分,乙氧苯草胺与丙嗪嘧磺隆的质量比为1:60~60:1。本发明还公开了该除草组合物在水稻田苗后除草中的应用,特别是在防除水稻田中禾本科和阔叶杂草中的应用。本发明除草组合物用于水稻田苗后除草,特别是用于防除水稻田中禾本科和阔叶杂草具有显著效果,相对于单剂在提高了药效的前提下,延缓杂草抗性,除草谱广,持效期长,而且对水稻以及后茬作物都具有安全性。The invention discloses a herbicidal composition containing rimsulfuron-methyl and ethoxyfen, the herbicidal composition uses rimsulfuron-methyl and ethoxyfen as main active ingredients, The mass ratio of promethazone-methyl is 1:60-60:1. The invention also discloses the application of the herbicidal composition in post-emergence weeding in paddy fields, especially the application in controlling gramineous and broad-leaved weeds in paddy fields. The herbicidal composition of the present invention is used for post-emergence weeding in paddy fields, especially for controlling gramineous and broad-leaved weeds in paddy fields. It has a wide spectrum, a long duration of effect, and is safe for rice and subsequent crops.
Description
技术领域technical field
本发明属于农药技术领域,尤其是除草剂领域,具体涉及一种含丙嗪嘧磺隆与乙氧苯草胺的二元复配除草组合物,该除草组合物可应用于水稻田苗后除草。The invention belongs to the technical field of pesticides, in particular to the field of herbicides, and in particular relates to a binary compound herbicidal composition containing promasulfuron-methyl and ethoxyfen, which can be used for post-emergence weeding in paddy fields.
背景技术Background technique
丙嗪嘧磺隆(propyrisulfuron),是一种选择性广谱除草剂,对耐磺酰脲类除草剂的杂草有较好的防除效果,对大龄稗草、莎草、阔叶草有效,可叶面喷雾、甩施。Propyrisulfuron is a selective broad-spectrum herbicide, which has a good control effect on weeds resistant to sulfonylurea herbicides, and is effective on older barnyardgrass, sedge, and broad-leaved grass. Can be foliar spray, shake application.
乙氧苯草胺,化学名称:2',3'-二氯-N-(4-乙氧基甲氧基苯酰)苯胺,结构式:Ethoxyfen, chemical name: 2',3'-dichloro-N-(4-ethoxymethoxybenzoyl)anilide, structural formula:
乙氧苯草胺属酰胺类除草剂,主要用于水稻田苗前或苗后除草。Ethoxyfen is an amide herbicide, which is mainly used for pre-emergence or post-emergence weeding in rice fields.
目前水稻田除草剂受作物安全性所限,杀草谱也有限,单独使用一种除草剂单剂不能完全有效地控制水稻田杂草的发生,再者有些除草剂由于水溶性大或田间持效期太长、用量过大或施药不均匀都容易造成对当季作物或后茬作物的残留毒害。发明人经研究发现,除草剂的增效复配是扩大杂草防除谱和提高防效的有效措施,迄今为止尚未发现有关丙嗪嘧磺隆与乙氧苯草胺复配的除草组合物。At present, herbicides in paddy fields are limited by the safety of crops, and the herbicidal spectrum is also limited. Using a single herbicide alone cannot completely and effectively control the occurrence of weeds in paddy fields. If the effective period is too long, the dosage is too large or the application is uneven, it will easily cause residual toxicity to the crops of the current season or the subsequent crops. The inventors have found through research that synergistic compounding of herbicides is an effective measure to expand the control spectrum of weeds and improve the control effect. Up to now, no herbicidal composition compounded with promasulfuron-methyl and ethoxyfen has been found.
发明内容Contents of the invention
本发明的目的是提供一种含丙嗪嘧磺隆与乙氧苯草胺的除草组合物。The object of the present invention is to provide a herbicidal composition containing promasulfuron-methyl and ethoxyfen.
本发明的另一目的是提供该除草组合物在水稻田除草中的应用。Another object of the present invention is to provide the application of the herbicidal composition in paddy field weeding.
本发明的目的通过以下技术方案实现:The object of the present invention is achieved through the following technical solutions:
一种含丙嗪嘧磺隆与乙氧苯草胺的除草组合物,该除草组合物以丙嗪嘧磺隆与乙氧苯草胺为主要有效成分,其中,乙氧苯草胺与丙嗪嘧磺隆的质量比为1:60~60:1。A herbicidal composition containing promasulfuron-methyl and ethopetazine, the herbicidal composition uses promethazone-methyl and ethopetazine as main active ingredients, wherein, ethopetazine and promethazine The mass ratio of rimsulfuron-methyl is 1:60~60:1.
本发明所述的除草组合物,所述的乙氧苯草胺与丙嗪嘧磺隆的质量比为1:30~50:1,进一步优选为1:30~29:1,最优选为1:5~20:1。In the herbicidal composition of the present invention, the mass ratio of ethoxyfen to promasulfuron-methyl is 1:30 to 50:1, more preferably 1:30 to 29:1, most preferably 1 :5~20:1.
在一些优选的技术方案中:乙氧苯草胺与丙嗪嘧磺隆可以在34:1、29:1、59:1、12:1、60:1、50:1、40:1、20:1、10:1、5:1、1:1、1:5、1:10、1:20、1:30、1:50、1:60这些比例中选择。In some preferred technical solutions: ethoxyfen and promethazone-methyl can be at 34:1, 29:1, 59:1, 12:1, 60:1, 50:1, 40:1, 20 :1, 10:1, 5:1, 1:1, 1:5, 1:10, 1:20, 1:30, 1:50, 1:60.
在本发明除草组合物中,所述的丙嗪嘧磺隆与乙氧苯草胺二者在除草组合物中的质量百分含量为1%~80%,优选为10%~65%。In the herbicidal composition of the present invention, the mass percentage of both promasulfuron-methyl and ethoxyfen in the herbicidal composition is 1%-80%, preferably 10%-65%.
本发明所述的除草组合物以丙嗪嘧磺隆与乙氧苯草胺为有效成分,还可以添加农药制剂上允许的常规表面活性剂、增稠剂、溶剂或固体填料等助剂配制成农药上允许的任意一种剂型。优选加工成乳油、悬浮剂、水乳剂、微乳剂、水分散粒剂、可湿性粉剂等。The herbicidal composition of the present invention uses promasulfuron-methyl and ethoxyfen as active ingredients, and can also be prepared by adding conventional surfactants, thickeners, solvents or solid fillers allowed on pesticide formulations. Any dosage form allowed on pesticides. It is preferably processed into emulsifiable concentrate, suspension concentrate, water emulsion, microemulsion, water dispersible granule, wettable powder, etc.
本发明所述的除草组合物可只含有活性成分丙嗪嘧磺隆与乙氧苯草胺,以丙嗪嘧磺隆与乙氧苯草胺为有效成分进行二元复配,也可在使用或配制时向组合物中加入其他活性组分,该除草组合物中的有效成份以增效有效量存在于组合物中。The herbicidal composition of the present invention may only contain the active ingredients promasulfuron-methyl and acetofen, and use promethazone-methyl and acetofen as active ingredients for binary compounding, and may also be used in Or add other active components to the composition during preparation, and the active ingredients in the herbicidal composition are present in the composition in a synergistically effective amount.
本发明的除草组合物,应用于水稻田除草,其能够防除水稻田中各种禾本科和阔叶杂草,具有显著效果,在提高了药效的前提下,对水稻以及后茬作物都具有安全性。因此,本发明的另一个效果是提供所述的除草组合物在水稻田苗后除草中的应用,特别是在防除水稻田中禾本科和阔叶杂草中的应用。本发明所述的除草组合物用于制备水稻田苗后除草的除草剂,特别是用于制备防除水稻田中禾本科和阔叶杂草的除草剂。所述的杂草为马唐、稗草、狗尾草、鸭舌草、千金子。The herbicidal composition of the present invention is applied to weeding in paddy fields, and it can prevent and control various gramineous and broad-leaved weeds in paddy fields, and has remarkable effects. sex. Therefore, another effect of the present invention is to provide the application of the herbicidal composition in post-emergence weeding in paddy fields, especially the application in controlling gramineous and broad-leaved weeds in paddy fields. The herbicidal composition of the invention is used for preparing herbicides for post-emergence weeding in paddy fields, especially for preparing herbicides for controlling gramineous and broad-leaved weeds in paddy fields. The weeds are crabgrass, barnyardgrass, green foxtail, bermudagrass, and daughter of a daughter.
本发明所述的除草组合物可The herbicidal composition of the present invention can be
和现有技术相比,本发明的有益效果:Compared with prior art, the beneficial effect of the present invention:
本发明选择可杀草谱不同,优缺点互补的丙嗪嘧磺隆与乙氧苯草胺两种除草剂适当减量后配成合剂使用,这样既扩大了杀草谱,明显提高了除草效果,也避免了对当季作物产生药害和对后茬作物产生残留毒害的可能性。具体表现为以下优点:In the present invention, two herbicides, promasulfuron-methyl and ethoxyfen, which have different herbicidal spectrums and have complementary advantages and disadvantages, are selected to be used as a mixture after appropriate reduction, so that the herbicidal spectrum is expanded and the herbicidal effect is obviously improved. , It also avoids the possibility of phytotoxicity to current crops and residual toxicity to subsequent crops. The specific performance is as follows:
1、除草活性高。本发明的除草组合物可以通过两种不同机理杀死杂草,使得杂草抗性产生速度降低了,极大地提高除草剂的杀草活性。1. High herbicidal activity. The herbicidal composition of the present invention can kill weeds through two different mechanisms, so that the speed of weed resistance generation is reduced, and the herbicidal activity of the herbicide is greatly improved.
2、除草谱广,持效期长。两者混合后,能够提高对多种禾本科杂草和阔叶杂草的防治。2. Broad herbicide spectrum and long duration. The combination of the two can improve the control of a variety of grass weeds and broadleaf weeds.
3、延缓杂草抗性。本发明除草组合物通过二元复配,降低杂草对药剂的抗性,并提高对抗性杂草的防效,从而延长药剂的使用寿命。3. Delay weed resistance. The herbicidal composition of the present invention reduces the resistance of weeds to the chemical agent and improves the control effect of the resistant weed through binary compounding, thereby prolonging the service life of the chemical agent.
4、安全性高。由于其使用剂量得到了控制,使药剂在提高了药效的前提下,其对水稻以及后茬作物的安全性也得到了提高。4. High security. Because the dose is controlled, the safety of the medicament to rice and subsequent crops is also improved under the premise of improving the efficacy of the medicament.
具体实施方式detailed description
为了使本发明的目的、技术方案及优点更加清楚明白,以下结合实施例,对本发明进行进一步详细说明。应当理解,此处所描述的具体实施例仅用以解释本发明,并不用于限定本发明,凡在本发明的构思前提下对本发明制备方法的简单改进都属于本发明的保护范围之内。In order to make the object, technical solution and advantages of the present invention more clear, the present invention will be further described in detail below in conjunction with the examples. It should be understood that the specific examples described here are only used to explain the present invention, and are not used to limit the present invention. Any simple improvement to the preparation method of the present invention under the concept of the present invention falls within the protection scope of the present invention.
以下实施例所有配方中百分比均为质量百分含量。本发明组合物各种制剂的加工工艺均为现有技术,根据不同情况可以有所变化。Percentages in all formulations of the following examples are mass percentages. The processing techniques of various preparations of the composition of the present invention are prior art, and can be changed according to different situations.
一、剂型制备实施例One, dosage form preparation embodiment
实施例1:35%乙氧苯草胺·丙嗪嘧磺隆乳油(34:1)Example 1: 35% Ethoxyfen Promethazone-methyl EC (34:1)
乙氧苯草胺34%、丙嗪嘧磺隆1%、烷基酚聚氧乙烯醚4%、苯乙基酚聚氧乙烯醚15%,二甲苯补足至100%,按照常规的制剂方法配制成质量百分含量为35%的乳油。Ethoxyfen 34%, promethazone 1%, alkylphenol polyoxyethylene ether 4%, phenethylphenol polyoxyethylene ether 15%, xylene supplemented to 100%, prepared according to conventional preparation methods It is 35% emulsifiable concentrate by mass percentage.
实施例2:30%乙氧苯草胺·丙嗪嘧磺隆悬浮剂(29:1)Example 2: 30% Ethoxyfen Promethazone Suspension Concentrate (29:1)
乙氧苯草胺29%、丙嗪嘧磺隆1%、甲基萘磺酸钠甲醛缩合物6%、壬基酚聚氧乙烯醚3%、硅酸镁铝0.5%、乙二醇7%、磷酸三丁酯2%、硅油0.2%,余量为水,按照常规的制剂方法配制成质量百分含量为30%的悬浮剂。Ethoxyfen 29%, Promethazone 1%, Sodium Naphthalene Sulfonate Formaldehyde Condensate 6%, Nonylphenol Polyoxyethylene Ether 3%, Magnesium Aluminum Silicate 0.5%, Ethylene Glycol 7% , 2% of tributyl phosphate, 0.2% of silicone oil, and the balance is water, which is prepared into a suspending agent with a mass percentage of 30% according to a conventional preparation method.
实施例3:60%乙氧苯草胺·丙嗪嘧磺隆水分散粒剂(59:1)Example 3: 60% Ethoxyfen Promethazone-methyl Water-dispersible Granules (59:1)
乙氧苯草胺59%、丙嗪嘧磺隆1%、NNO(亚甲基双萘磺酸钠)5%、硫酸铵3%、聚乙烯醇2%,高岭土补足至100%,按照常规的制剂方法配制成质量百分含量为60%的水分散粒剂(WDG)。Ethoxyfen 59%, promethazone 1%, NNO (sodium methylene bis-naphthalene sulfonate) 5%, ammonium sulfate 3%, polyvinyl alcohol 2%, kaolin supplemented to 100%, according to the conventional Preparation method Prepare water dispersible granules (WDG) with a mass percentage of 60%.
实施例4:65%乙氧苯草胺·丙嗪嘧磺隆可湿性粉剂(12:1)Example 4: 65% Ethoxyfen Promethazone-methyl WP (12:1)
乙氧苯草胺60%、丙嗪嘧磺隆5%、NNO 6%、木质素磺酸钠4%,高岭土补足至100%,按照常规的制剂方法配制成质量百分含量为65%的可湿性粉剂(WP)。Ethoxyfen 60%, promasulfuron-methyl 5%, NNO 6%, sodium lignosulfonate 4%, kaolin supplemented to 100%, according to the conventional preparation method, the mass percentage content is 65%. Wet powder (WP).
实施例5:61%乙氧苯草胺·丙嗪嘧磺隆乳油(60:1)Example 5: 61% Ethoxyfen Promethazone-methyl EC (60:1)
乙氧苯草胺60%、丙嗪嘧磺隆1%、烷基酚聚氧乙烯醚4%、苯乙基酚聚氧乙烯醚15%,二甲苯补足至100%,按照常规的制剂方法配制成质量百分含量为61%的乳油。Ethoxyfen 60%, promethazone 1%, alkylphenol polyoxyethylene ether 4%, phenethylphenol polyoxyethylene ether 15%, xylene supplemented to 100%, prepared according to conventional preparation methods It is 61% emulsifiable concentrate by mass percentage.
实施例6:61%乙氧苯草胺·丙嗪嘧磺隆乳油(1:60)Example 6: 61% Ethoxyfen Promethazone-methyl EC (1:60)
乙氧苯草胺1%、丙嗪嘧磺隆60%、烷基酚聚氧乙烯醚4%、苯乙基酚聚氧乙烯醚15%,二甲苯补足至100%,按照常规的制剂方法配制成质量百分含量为61%的乳油。Ethoxyfen 1%, promethazone 60%, alkylphenol polyoxyethylene ether 4%, phenethylphenol polyoxyethylene ether 15%, xylene supplemented to 100%, prepared according to conventional preparation methods It is 61% emulsifiable concentrate by mass percentage.
实施例7:51%乙氧苯草胺·丙嗪嘧磺隆悬浮剂(50:1)Example 7: 51% Ethoxyfen Promethazone-methyl Suspension Concentrate (50:1)
乙氧苯草胺50%、丙嗪嘧磺隆1%、甲基萘磺酸钠甲醛缩合物6%、壬基酚聚氧乙烯醚3%、硅酸镁铝0.5%、乙二醇7%、磷酸三丁酯2%、硅油0.2%,余量为水,按照常规的制剂方法配制成质量百分含量为51%的悬浮剂。Ethoxyfen 50%, Promethazone 1%, Sodium Naphthalene Sulfonate Formaldehyde Condensate 6%, Nonylphenol Polyoxyethylene Ether 3%, Magnesium Aluminum Silicate 0.5%, Ethylene Glycol 7% , 2% of tributyl phosphate, 0.2% of silicone oil, and the balance is water, which is prepared into a suspending agent with a mass percentage of 51% according to a conventional preparation method.
实施例8:51%乙氧苯草胺·丙嗪嘧磺隆悬浮剂(1:50)Example 8: 51% Ethoxyfen Promethazone-methyl Suspension Concentrate (1:50)
乙氧苯草胺1%、丙嗪嘧磺隆50%、甲基萘磺酸钠甲醛缩合物6%、壬基酚聚氧乙烯醚3%、硅酸镁铝0.5%、乙二醇7%、磷酸三丁酯2%、硅油0.2%,余量为水,按照常规的制剂方法配制成质量百分含量为51%的悬浮剂。Ethoxyfen 1%, promethazone 50%, sodium methylnaphthalene sulfonate formaldehyde condensate 6%, nonylphenol polyoxyethylene ether 3%, magnesium aluminum silicate 0.5%, ethylene glycol 7% , 2% of tributyl phosphate, 0.2% of silicone oil, and the balance is water, which is prepared into a suspending agent with a mass percentage of 51% according to a conventional preparation method.
实施例9:31%乙氧苯草胺·丙嗪嘧磺隆水分散粒剂(1:30)Example 9: 31% Ethoxyfen Promethazone-methyl Water Dispersible Granules (1:30)
乙氧苯草胺1%、丙嗪嘧磺隆30%、NNO 5%、硫酸铵3%、聚乙烯醇2%,高岭土补足至100%,按照常规的制剂方法配制成质量百分含量为31%的水分散粒剂。Ethoxyfen 1%, promethazone 30%, NNO 5%, ammonium sulfate 3%, polyvinyl alcohol 2%, kaolin supplemented to 100%, according to the conventional preparation method to prepare a mass percentage of 31% % of water dispersible granules.
实施例10:41%乙氧苯草胺·丙嗪嘧磺隆水分散粒剂(40:1)Example 10: 41% Ethoxyfen Promethazone-methyl Water Dispersible Granules (40:1)
乙氧苯草胺40%、丙嗪嘧磺隆1%、NNO 5%、硫酸铵3%、聚乙烯醇2%,高岭土补足至100%,按照常规的制剂方法配制成质量百分含量为41%的水分散粒剂。Ethoxyfen 40%, promethazone 1%, NNO 5%, ammonium sulfate 3%, polyvinyl alcohol 2%, kaolin supplemented to 100%, prepared according to the conventional preparation method with a mass percentage of 41% % of water dispersible granules.
实施例11:42%乙氧苯草胺·丙嗪嘧磺隆可湿性粉剂(20:1)Example 11: 42% Ethoxyfen Promethazone-methyl WP (20:1)
乙氧苯草胺40%、丙嗪嘧磺隆2%、NNO 6%、木质素磺酸钠4%,高岭土补足至100%,按照常规的制剂方法配制成质量百分含量为42%的可湿性粉剂。Ethoxyfen 40%, promethazone 2%, NNO 6%, sodium lignosulfonate 4%, kaolin supplemented to 100%, according to the conventional preparation method, the mass percentage content is 42%. Wet powder.
实施例12:21%乙氧苯草胺·丙嗪嘧磺隆可湿性粉剂(1:20)Example 12: 21% Ethoxyfen Promethazone-methyl WP (1:20)
乙氧苯草胺1%、丙嗪嘧磺隆20%、NNO 6%、木质素磺酸钠4%,高岭土补足至100%,按照常规的制剂方法配制成质量百分含量为21%的可湿性粉剂。Ethoxyfen 1%, promethazone 20%, NNO 6%, sodium lignosulfonate 4%, kaolin supplemented to 100%, according to the conventional preparation method, the mass percentage content is 21%. Wet powder.
实施例13:33%乙氧苯草胺·丙嗪嘧磺隆水乳剂(1:10)Example 13: 33% Ethoxyfen Promethazone Emulsion in Water (1:10)
乙氧苯草胺3%、丙嗪嘧磺隆30%、甲基萘磺酸钠甲醛缩合物6%、壬基酚聚氧乙烯醚3%、硅酸镁铝0.5%、乙二醇7%、磷酸三丁酯2%、150#溶剂油20%,水补足至100%,按照常规的制剂方法配制成质量百分含量为33%的水乳剂。Ethoxyfen 3%, Promethazone 30%, Sodium Naphthalene Sulfonate Formaldehyde Condensate 6%, Nonylphenol Polyoxyethylene Ether 3%, Magnesium Aluminum Silicate 0.5%, Ethylene Glycol 7% , tributyl phosphate 2%, 150# solvent naphtha 20%, water supplements to 100%, is mixed with the water emulsion that mass percent composition is 33% according to routine preparation method.
实施例14:33%乙氧苯草胺·丙嗪嘧磺隆水乳剂(10:1)Example 14: 33% Ethoxyfen Promethazone Emulsion in Water (10:1)
乙氧苯草胺30%、丙嗪嘧磺隆3%、甲基萘磺酸钠甲醛缩合物6%、壬基酚聚氧乙烯醚3%、硅酸镁铝0.5%、乙二醇7%、磷酸三丁酯2%、150#溶剂油20%,水补足至100%,按照常规的制剂方法配制成质量百分含量为33%的水乳剂。Ethoxyfen 30%, Promethazone 3%, Sodium Naphthalene Sulfonate Formaldehyde Condensate 6%, Nonylphenol Polyoxyethylene Ether 3%, Magnesium Aluminum Silicate 0.5%, Ethylene Glycol 7% , tributyl phosphate 2%, 150# solvent naphtha 20%, water supplements to 100%, is mixed with the water emulsion that mass percent composition is 33% according to routine preparation method.
实施例15:30%乙氧苯草胺·丙嗪嘧磺隆微乳剂(5:1)Example 15: 30% Ethoxyfen Promethazone-methyl Microemulsion (5:1)
乙氧苯草胺25%、丙嗪嘧磺隆5%、甲基萘磺酸钠甲醛缩合物6%、壬基酚聚氧乙烯醚3%、硅酸镁铝0.5%、乙二醇7%、磷酸三丁酯2%,水补足至100%,按照常规的制剂方法配制成质量百分含量为30%的微乳剂。Ethoxyfen 25%, Promethazone 5%, Sodium Naphthalene Sulfonate Formaldehyde Condensate 6%, Nonylphenol Polyoxyethylene Ether 3%, Magnesium Aluminum Silicate 0.5%, Ethylene Glycol 7% , 2% of tributyl phosphate, supplemented with water to 100%, and prepared into a microemulsion with a mass percentage of 30% according to a conventional preparation method.
实施例16:60%乙氧苯草胺·丙嗪嘧磺隆可湿性粉剂(1:5)Example 16: 60% Ethoxyfen Promethazone-methyl WP (1:5)
乙氧苯草胺10%、丙嗪嘧磺隆50%、NNO 6%、木质素磺酸钠4%,高岭土补足至100%,按照常规的制剂方法配制成质量百分含量为60%的可湿性粉剂。Ethoxyfen 10%, promethazone 50%, NNO 6%, sodium lignosulfonate 4%, kaolin supplemented to 100%, prepared according to the conventional preparation method with a mass percentage of 60%. Wet powder.
实施例17:10%乙氧苯草胺·丙嗪嘧磺隆可湿性粉剂(1:1)Example 17: 10% Ethoxyfen Promethazone-methyl WP (1:1)
乙氧苯草胺5%、丙嗪嘧磺隆5%、NNO 6%、木质素磺酸钠4%,高岭土补足至100%,按照常规的制剂方法配制成质量百分含量为10%的可湿性粉剂。Ethoxyfen 5%, promethazone 5%, NNO 6%, sodium lignosulfonate 4%, kaolin supplemented to 100%, according to the conventional preparation method, the mass percentage content of 10% can be prepared Wet powder.
二、药效验证试验2. Drug efficacy verification test
1)、室内活性测定试验1), indoor activity determination test
按照有效成分乙氧苯草胺:丙嗪嘧磺隆质量配比为:70:1,34:1、29:1、59:1、12:1、60:1、50:1、40:1、20:1、10:1、5:1、1:1、1:5、1:10、1:20、1:30、1:50、1:60,1:70进行试验,测定其对水稻田常见杂草稗草的共毒系数。According to the mass ratio of the active ingredient ethoxyfen: promethazone-methyl: 70:1, 34:1, 29:1, 59:1, 12:1, 60:1, 50:1, 40:1 , 20:1, 10:1, 5:1, 1:1, 1:5, 1:10, 1:20, 1:30, 1:50, 1:60, 1:70 were tested to determine the Co-toxicity coefficient of barnyardgrass, a common weed in paddy fields.
试验方法:将定量的稗草的种子分别播种于9cm的一次性纸杯中,每杯中播种10~15粒种子,在光照培养箱中培养,待稗草1-4叶期时,在履带式作物喷雾机上进行喷雾处理。处理后温室内继续培养,定期观察各处理对杂草的防除效果,30d后称量各处理后的杂草鲜重,计算其毒力回归曲线和共毒系数。共毒系数大于120,表明两种有效物质具有增效作用,共毒系数在80-120之间,表明两种有效物质具有相加作用,共毒系数小于80,表明两种有效物质具有拮抗作用。测定结果如表1所示。Test method: sow quantitative barnyardgrass seeds in 9cm disposable paper cups, sow 10-15 seeds in each cup, and cultivate them in a light incubator. Spray treatment on crop sprayer. After the treatment, the cultivation was continued in the greenhouse, and the control effect of each treatment on weeds was regularly observed. After 30 days, the fresh weight of the weeds after each treatment was weighed, and the regression curve of toxicity and the co-toxicity coefficient were calculated. A co-toxicity coefficient greater than 120 indicates that the two effective substances have a synergistic effect, a co-toxicity coefficient between 80-120 indicates that the two effective substances have an additive effect, and a co-toxicity coefficient of less than 80 indicates that the two effective substances have an antagonistic effect . The measurement results are shown in Table 1.
表1 室内活性测定结果Table 1 The results of indoor activity determination
从表1可以看出,乙氧苯草胺与丙嗪嘧磺隆按照质量比1:60~60:1复配对稗草的除草效果显著提高,说明二者复配对防除稗草具有显著的增效作用。当乙氧苯草胺与丙嗪嘧磺隆的配比在1:30~50:1之间,两种有效物质复配后的共毒系数较优,共毒系数不低于135;当乙氧苯草胺与丙嗪嘧磺隆的配比在1:30~29:1之间,共毒系数大于150;当乙氧苯草胺与丙嗪嘧磺隆的配比在1:5~29:1之间,共毒系数大于160;说明本发明具有明显的增效作用。It can be seen from Table 1 that the combination of ethoxyfen and promethazone-methyl at a mass ratio of 1:60-60:1 significantly improved the herbicidal effect on barnyard grass, indicating that the combination of the two had a significant increase in the control of barnyard grass. effect. When the ratio of ethoxyfen to promasulfuron-methyl is between 1:30 and 50:1, the co-toxicity coefficient of the two effective substances after compounding is better, and the co-toxicity coefficient is not less than 135; when B The ratio of oxetam to promethazone is between 1:30 and 29:1, and the co-toxicity coefficient is greater than 150; Between 29:1, the co-toxicity coefficient is greater than 160; indicating that the present invention has obvious synergistic effect.
2)、田间药效试验。2), field efficacy test.
供试药剂:Drugs for testing:
实施例1~17制备的丙嗪嘧磺隆与乙氧苯草胺不同配比的二元复配除草剂。Binary compound herbicides prepared in Examples 1-17 with different ratios of promasulfuron-methyl and ethoxyfen.
对照药剂:Comparative drug:
9.5%丙嗪嘧磺隆SC(市售),40%乙氧苯草胺水分散粒剂(采用常规方法制备)。9.5% promasulfuron-methyl SC (commercially available), 40% ethoxyfen water-dispersible granules (prepared by conventional methods).
供试作物:水稻Test crops: rice
水稻苗长势良好,植株健壮,无其他病虫害。The rice seedlings are growing well, the plants are robust, and there are no other diseases and insect pests.
防除对象:Prevention object:
马唐、稗草、鸭舌草、狗尾草、千金子等杂草。Weeds such as crabgrass, barnyardgrass, bermudagrass, foxtail, and daughter.
试验方法:experiment method:
按照试验小区的面积,准确称量好各种药剂,并兑水稀释后,利用背负式喷雾器,进行均匀喷雾,喷头选用除草剂专用的扇形喷头。喷雾时,要注意将药液均匀喷施到试验小区中,做到没有漏喷、多喷的现象。Accurately weigh various agents according to the area of the test plot, and after diluting with water, use a knapsack sprayer to spray evenly, and the nozzles are herbicide-specific fan-shaped nozzles. When spraying, pay attention to spraying the liquid medicine evenly into the test area, so that there is no leakage or overspray.
试验后分别在药后20d、40d观察杂草死亡情况,并比较各种药剂的除草活性。此外,还要在药后1~15d内观察作物的生产情况(用量均为每亩地有效成分的用量),以考察药剂对作物是否有药害。After the test, weed death was observed at 20 days and 40 days after application, and the herbicidal activities of various agents were compared. In addition, it is necessary to observe the production of crops within 1-15 days after application (the dosage is the amount of active ingredients per mu of land) to investigate whether the pesticide has phytotoxicity on the crops.
本发明的实施例制剂除草试验效果见下表2(药后20d)和表3(药后40d)。The herbicidal test effects of the preparations of the embodiments of the present invention are shown in Table 2 (after 20 d) and Table 3 (40 d) below.
表2 田间药效试验结果(药后20d)Table 2 Field drug efficacy test results (20 days after drug treatment)
表3 田间药效试验结果(药后40d)Table 3 Field drug efficacy test results (40 days after drug treatment)
从表2和表3可以看出,丙嗪嘧磺隆与乙氧苯草胺复配具有起效快、扩大除草谱和提高除草活性的作用,并延长了药剂的持效期。能有效防除阔叶杂草和禾本科杂草,其防除效果优于单剂的防效,说明二者复配对水稻田中阔叶杂草和禾本科杂草的防除效果有显著的增效作用。It can be seen from Table 2 and Table 3 that the combination of promasulfuron-methyl and ethoxyfen has the effects of rapid onset of action, expansion of herbicidal spectrum and improvement of herbicidal activity, and prolongs the duration of the agent. It can effectively control broad-leaved weeds and gramineous weeds, and its control effect is better than that of a single agent, indicating that the combination of the two has a significant synergistic effect on the control of broad-leaved weeds and gramineous weeds in rice fields.
表4 药剂对作物的安全性调查结果Table 4 Results of survey on the safety of pesticides on crops
各处理小区内的水稻长势良好,未见任何药斑,说明各种药剂对水稻均安全。The rice in each treatment plot grew well, and no drug spots were seen, indicating that various pesticides are safe to rice.
Claims (10)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710133335.4A CN106922715A (en) | 2017-03-08 | 2017-03-08 | A kind of Herbicidal combinations of Sulfometuron Methyl containing promazine with ethobenzanid and its application |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710133335.4A CN106922715A (en) | 2017-03-08 | 2017-03-08 | A kind of Herbicidal combinations of Sulfometuron Methyl containing promazine with ethobenzanid and its application |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN106922715A true CN106922715A (en) | 2017-07-07 |
Family
ID=59423423
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201710133335.4A Pending CN106922715A (en) | 2017-03-08 | 2017-03-08 | A kind of Herbicidal combinations of Sulfometuron Methyl containing promazine with ethobenzanid and its application |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN106922715A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109699668A (en) * | 2019-02-25 | 2019-05-03 | 安徽省农业科学院植物保护与农产品质量安全研究所 | A kind of ternary weeding composition and its application for paddy field weed |
| WO2024110852A1 (en) * | 2022-11-25 | 2024-05-30 | Upl Limited | A herbicidal composition and a process for preparing the same thereof |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200513183A (en) * | 2003-09-30 | 2005-04-16 | Sumitomo Chem Takeda Agro Co | Herbicide composition |
| CN100349517C (en) * | 2002-01-18 | 2007-11-21 | 住化武田农药株式会社 | Fused heterocyclic sulfonylurea compound, herbicide containing the same and method of controlling weed with the same |
| JP2017019844A (en) * | 2016-03-22 | 2017-01-26 | 住友化学株式会社 | Herbicidal composition |
-
2017
- 2017-03-08 CN CN201710133335.4A patent/CN106922715A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100349517C (en) * | 2002-01-18 | 2007-11-21 | 住化武田农药株式会社 | Fused heterocyclic sulfonylurea compound, herbicide containing the same and method of controlling weed with the same |
| TW200513183A (en) * | 2003-09-30 | 2005-04-16 | Sumitomo Chem Takeda Agro Co | Herbicide composition |
| JP2017019844A (en) * | 2016-03-22 | 2017-01-26 | 住友化学株式会社 | Herbicidal composition |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109699668A (en) * | 2019-02-25 | 2019-05-03 | 安徽省农业科学院植物保护与农产品质量安全研究所 | A kind of ternary weeding composition and its application for paddy field weed |
| WO2024110852A1 (en) * | 2022-11-25 | 2024-05-30 | Upl Limited | A herbicidal composition and a process for preparing the same thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN106922715A (en) | A kind of Herbicidal combinations of Sulfometuron Methyl containing promazine with ethobenzanid and its application | |
| CN107027791A (en) | The Herbicidal combinations of a kind of Sulfometuron Methyl containing promazine and benzobicylon and its application | |
| CN106889083A (en) | A kind of Herbicidal combinations and its application containing pyraclonil and clomazone | |
| CN108077295A (en) | A kind of Herbicidal combinations and its application containing primisulfuronmethyl and ring sulphur ketone | |
| CN106857609A (en) | A kind of Herbicidal combinations and its application containing pyraclonil and ethoxysulfuron | |
| CN107156124A (en) | A kind of Herbicidal combinations and its application containing the bicyclic ketone of benzo and butachlor | |
| CN107047597A (en) | The Herbicidal combinations of a kind of Sulfometuron Methyl containing promazine and Diflufenican and its application | |
| CN106818795A (en) | A kind of Herbicidal combinations and its application containing pyraclonil and ethobenzanid | |
| CN106962383A (en) | The Herbicidal combinations of a kind of Sulfometuron Methyl containing promazine and triaziflam and its application | |
| CN107926970A (en) | A kind of sulphur of ketone containing thiophene is grand with the Herbicidal combinations of isopropyl methoxalamine and its application | |
| CN107047592A (en) | A kind of Herbicidal combinations and its application containing pyraclonil and bensulfuron-methyl | |
| CN107047595A (en) | The Herbicidal combinations of a kind of Sulfometuron Methyl containing promazine and clomazone and its application | |
| CN106889094A (en) | A kind of Herbicidal combinations and its application containing pyraclonil and pyrazosulfuron | |
| CN106900734A (en) | A kind of Herbicidal combinations of Sulfometuron Methyl containing promazine with fentrazamide and its application | |
| CN106922717A (en) | A kind of Herbicidal combinations of Sulfometuron Methyl containing promazine with ethoxysulfuron and its application | |
| CN107027792A (en) | The Herbicidal combinations of a kind of Sulfometuron Methyl containing promazine and esprocarb and its application | |
| CN107810966A (en) | A kind of Herbicidal combinations and its application containing primisulfuronmethyl and thifensulfuronmethyl | |
| CN108617680A (en) | A kind of Herbicidal combinations and its application of Sulfometuron Methyl containing formamido group and tritosulfuron | |
| CN107926967A (en) | A kind of Herbicidal combinations and its application containing primisulfuronmethyl and alachlor | |
| CN106900732A (en) | A kind of Herbicidal combinations of Sulfometuron Methyl containing promazine with dithiopyr and its application | |
| CN106857577A (en) | A kind of Herbicidal combinations and its application containing pyraclonil and dithiopyr | |
| CN107027793A (en) | A herbicidal composition containing promasulfuron-methyl and acetochlor and its application | |
| CN106889098A (en) | A kind of Herbicidal combinations of Sulfometuron Methyl containing promazine with symetryne and its application | |
| CN106857600A (en) | A kind of Herbicidal combinations and its application containing pyraclonil and isoproturon | |
| CN108576036A (en) | A kind of Herbicidal combinations and its application of Sulfometuron Methyl containing formamido group and bentazone |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20170707 |
|
| RJ01 | Rejection of invention patent application after publication |