CN107372551B - Weeding composition containing triazophorbine and pyridazine compound and application thereof - Google Patents

Weeding composition containing triazophorbine and pyridazine compound and application thereof Download PDF

Info

Publication number
CN107372551B
CN107372551B CN201710744235.5A CN201710744235A CN107372551B CN 107372551 B CN107372551 B CN 107372551B CN 201710744235 A CN201710744235 A CN 201710744235A CN 107372551 B CN107372551 B CN 107372551B
Authority
CN
China
Prior art keywords
triazophone
pyridazine
active ingredient
weeding
pyridazine compounds
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.)
Active
Application number
CN201710744235.5A
Other languages
Chinese (zh)
Other versions
CN107372551A (en
Inventor
连磊
张景远
彭学岗
刘娜
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Qingdao Kingagroot Chemical Compound Co Ltd
Original Assignee
Qingdao Kingagroot Chemical Compound Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Qingdao Kingagroot Chemical Compound Co Ltd filed Critical Qingdao Kingagroot Chemical Compound Co Ltd
Priority to CN201710744235.5A priority Critical patent/CN107372551B/en
Priority to PCT/CN2017/112010 priority patent/WO2019037313A1/en
Publication of CN107372551A publication Critical patent/CN107372551A/en
Application granted granted Critical
Publication of CN107372551B publication Critical patent/CN107372551B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/561,2-Diazoles; Hydrogenated 1,2-diazoles
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/02Biocides, 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 no bond to a nitrogen atom
    • A01N47/06Biocides, 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 no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/18Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring

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

The invention belongs to the field of pesticides, and particularly relates to a weeding composition containing triazophos-cotrione and pyridazine compounds and application thereof. The weeding composition comprises an active ingredient A and an active ingredient B which are used for weeding effective dose, wherein the active ingredient A is the triazasulamone, and the active ingredient B is a pyridazine compound selected from pyridate or cycloprominate. The composition can effectively prevent and kill the problems of black nightshade, moleplant seed, rice barnyard grass, barnyard grass and other weeds in a paddy field, and has the characteristics of expanding a weed control spectrum, reducing the application amount, being safe to crops, generating a synergistic effect, solving resistant weeds and the like.

Description

Weeding composition containing triazophorbine and pyridazine compound and application thereof
Technical Field
The invention belongs to the field of pesticides, and particularly relates to a weeding composition containing triazophos-cotrione and pyridazine compounds and application thereof.
Background
Chemical weeding is the most economic and effective means in preventing and removing weeds in farmlands, but the problems of drug resistance and resistance evolution of weeds and the like are easily caused by using a single variety or a single action mode of chemical herbicide continuously at a high dose for a long time.
The chemical structural formula of the triazophone is shown as
Figure BDA0001389781420000011
The HPPD inhibitor herbicide is a newly developed HPPD inhibitor herbicide for post-emergence stem and leaf treatment of the paddy field, has excellent biological activity, and can effectively prevent and kill various malignant weeds in the paddy field.
The chemical structural formula of the pyridate is
Figure BDA0001389781420000012
Is a selective post-emergence herbicide. After the treatment of the stem and leaf, the stem and leaf are quickly absorbed by the leaf, the Hill reaction of photosynthesis is blocked, the leaf of the weed turns yellow and stops growing, and the weed withers and dies. Is suitable for preventing and killing broad-leaved weeds of cereal crops such as wheat, rice, corn and the like, and particularly has good preventing and killing effect on cleavers, amaranthus retroflexus and certain local weeds.
The structural formula of the compound cyclopyromate (test code number H-965) is shown in the specification
Figure BDA0001389781420000013
Is a pyridazine herbicide developed by Mitsui chemical Co., Ltd., Japan, and is a photosystem II inhibitor. The creation may be based on the structural derivation of pyridate and pyridaben.
The reasonable compounding or mixing of the herbicide compound has the advantages of expanding the weed spectrum, improving the control effect, delaying the occurrence and development of drug resistance and drug resistance of weeds and the like, and is one of the most effective methods for solving the problems. Therefore, the development of a weeding composition variety which has high safety and wide weed control spectrum, can produce synergistic effect and solve the problem of resistant weeds is urgently needed in production.
Disclosure of Invention
In order to solve the problems in the prior art, the invention provides a weeding composition containing triazophos and pyridazine compounds and application thereof. The composition can effectively prevent and kill the weeds such as nightshade, moleplant seed, rice barnyard grass and barnyard grass in crop fields, and has the characteristics of expanding the weed control spectrum, reducing the application amount, being safe to crops, generating synergistic effect and solving resistant weeds.
A weeding composition containing triazophos and pyridazine compounds comprises a herbicidally effective amount of an active ingredient A and an active ingredient B, wherein the active ingredient A is triazophos, and the active ingredient B is pyridazine compounds selected from pyridate or cyclopyromate.
Wherein the weight ratio of A to B is 1:120-120:1, preferably 1:100-100: 1; further, the weight ratio of A and B is 1:80-80:1, preferably 1:50-50: 1; further, the weight ratio of A and B is 1:20 to 20:1, preferably 1:10 to 10:1, more preferably 1:5 to 5: 1.
The mass percentage of A, B in the weeding composition accounts for 1-95% of the total amount, and preferably 10-80%.
The weeding composition also comprises conventional auxiliaries which comprise a carrier and a surfactant.
The term "carrier" herein denotes an organic or inorganic, natural or synthetic substance. They facilitate the application of the active ingredient, the carrier being generally inert and must be agriculturally acceptable, in particular for the treated plant. The carrier may be a solid, such as a clay, natural or synthetic silicate, silica, resin, wax, solid fertilizer, or the like; or liquids such as water, alcohols, ketones, petroleum distillates, aromatic or waxy hydrocarbons, chlorinated hydrocarbons, liquefied gases, etc.
Surfactants may include emulsifying, dispersing or wetting agents, which may be ionic or non-ionic. Examples which may be mentioned are salts of polyacrylic acids, lignosulphonates, salts of phenolsulphonic or naphthalenesulphonic acids, polymers of ethylene oxide with aliphatic alcohols or with aliphatic acids or with aliphatic amines and substituted phenols, in particular alkylphenols or arylphenols, sulphosuccinates, taurine derivatives, in particular taurine alkyl esters, and phosphoric esters of alcohols or polyhydroxyethylated phenols, alkylsulfonates, alkylarylsulphonates, alkylsulfates, lauryl ether sulphates, fatty alcohol sulphates, and sulphated hexadec, heptadeca-and octadecanols and sulphated fatty alcohol glycol ethers, and furthermore condensates of naphthalene or naphthalenesulphonic acids with phenol and formaldehyde, polyoxyethylene octylphenyl ether, ethoxylated isooctylphenol, octylphenol or nonylphenol, alkylphenyl polyglycol ethers, tributylphenyl polyglycol ether, tristearylphenyl polyglycol ether, polystearylphenyl polyglycol ether, Alkylaryl polyether alcohols, alcohol and fatty alcohol/ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignosulfite waste liquors, and also proteins, denatured proteins, polysaccharides (e.g. methylcellulose), hydrophobically modified starches, polyvinyl alcohols, polycarboxylates, polyalkoxylates, polyvinylamines, polyvinylpyrrolidone and copolymers thereof. At least one surfactant is required to be present to facilitate dispersion of the active ingredients in water and to facilitate their proper application to the plant.
The compositions may also contain various other components such as protective colloids, binders, thickeners, thixotropic agents, penetrating agents, stabilizers, chelating agents, dyes, colorants, and polymers.
The composition of the present invention may be diluted or used directly by the user prior to use. The formulation can be prepared by conventional processing methods, i.e., mixing the active substance with a liquid solvent or solid carrier, and adding one or more surfactants such as dispersing agent, stabilizer, wetting agent, binder, defoamer, etc.
The specific preparation of the weeding composition is dispersible oil suspending agent, water suspending agent, suspending emulsion, wettable powder, missible oil, water dispersible granules (dry suspending agent), emulsion in water and microemulsion.
In short, the compositions of the present invention may be mixed with solid and liquid additives conventionally used in prior art formulations.
In addition, the combination of compound a and pyridate and the combination of compound a and cycloprominate may be mixed with active substances known, for example, from "technical universe of new agricultural chemicals", chinese agro-scientific and technical press, 2010.9 and the references cited therein. For example the herbicide active substances mentioned below, (remarks: name of the compound, either common name according to the international organization for standardization (ISO) or chemical name, with a code number where appropriate): acetochlor, butachlor, alachlor, propisochlor, metolachlor, s-metolachlor, pretilachlor, propyzamide, pretilachlor, napropamide, R-levulinyl-propyzamide, propanil, mefenacet, dibenzamide, diflufenican, flumetsulam, bromobutyrolac, dimethenamid, mefenacet, metazachlor, isoxaflutole, ryegrass methyl ester, loflutolane, diacrylamide, pethoxamide, butachlor, propisochlor, cyprosulfamide, flumetsulam, heptanoyl, isobutramine, propyzamide, terbutamid, dimethenamid, larvamide, trimethylcyclam, clofenamid, propyzamide, penoxulamide, carpronide, diflormid, trinitrol, butachlor, butafenacet, butachlor, benfluralin, bencarbzamide, pencyhalonil, metolachlor, bencarbzamide, pencyhalonil, butachlor, benfluralin-bencarbzachlor, bencarbzamide, bencarb-N-P-N-P-N-P-N-, Grazing amine, bensulfuron, quinoxalamine, bensulfuron-methyl, naproxen, acetochlor, naphazel, thiachlor, pyraflufen, bensulfuron-methyl, prochloraz, clofenamide, butamidam, flupiram, atrazine, simazine, prometryn, cyanazine, simetryn, ametryn, prometryn, ipratron, flurazin, terbutryn, triazineone-flumetsulam, ciprofloxacin, glycazine, pradapazine, prometryn, simatong, azidezin, diuron, isopentetryn, cycloprozine, ametryn, terbuthylazine, terbuton, metocloprid, cyanazine, bentazon, clonazine, atrazine, metribuzin, cyanuric acid, indaziflazaflam, chlorsulfuron, meturon, bensulfuron, chlorimuron, tribenuron-methyl, thifensulfuron-methyl, pyrazosulfuron-methyl, sulfosulfuron-methyl, sulfometuron, bensulfuron-methyl, benazol-methyl, bensulfuron-methyl, benazol-methyl, benflurazid, benfluridimethyl, benfluridil, benflurazid, benfluridil, ben, Cinosulfuron, triasulfuron, sulfometuron-methyl, nicosulfuron, ethametsulfuron, amidosulfuron, ethoxysulfuron, cyclosulfamuron, rimsulfuron, azimsulfuron, primisulfuron-methyl, flusulfuron-methyl, flupyrsulfuron-methyl, epoxysulfuron, imazosulfuron, primisulfuron-methyl, prosulfuron, sulfosulfuron, trifloxysulfuron, triflusulfuron, metsulfuron-methyl sodium, flupyrazosulfuron, methisulfuron-methyl, primisulfuron, propysilfuron (Propyrisulfuron), metribusulfuron, acifluorfen-methyl, fomesafen, lactofen, fluoroglycofen-ethyl, oxyfen, prosulfuron, benfuresafen, trifloxysulfuron, metofen-ethyl, metofen, trifloxysulfuron, fluroxypyr, fluridone, benfop, benfluridone, benfurazolin, benfluridone, benfurbenfluridone, benfluridone, benfurin, benfluridone, benfurbenfurbenfurin, benfurbenfurbenfurbenfurbenfurbenfurin, benfluridone, benfurbenfurbenfurbenfurbenfurin, benfurin, benfluridone, benfurin, benfurbenfurbenfurin, benfurbenfurbenfurbenfurbenfurbenfurbenfurbenfurbenfurbenfurbenfurin, benfurin, benfurbenfurbenfurbenfurbenfurin, benfurin, benfurbenfurbenfurbenfurbenfurbenfurbenfurin, benfurin, benfurbenfurin, benfurin, benfurbenfurbenfurbenfurbenfurbenfurbenfurbenfurbenfurin, benfurin, benfurbenfurbenfurin, benfurbenfurbenfurbenfurbenfurin, benfurin, benfurbenfurin, benfurin, benfurbenfurbenfurin, benfurbenfurbenfurbenfurbenfurin, benfurin, benfurbenfurbenfurbenfur, Dimethofen, oxyfluorfen, clofenflurate, Halosafen, chlortoluron, isoproturon, linuron, diuron, sifenuron, fluometuron, benzthiauron, methabenzuron, prosulfuron, sulfosulfuron, clomauron, clodinafuron, clofensulfuron, metoxuron, bromuron, metoxuron, meturon, fensulfuron, prosulfuron, subtilon, cuarone, metolachlor, cycloaroron, cyclouron, thifluuron, buthiuron, kuron, cumuron, metoxuron, methamidothion, metominosulfuron, trifolium, isoxafluron, isoxauron, moneuronon, aniron, methicuron, chloretron, clotururon, teuron, benuron, pennison, phenmedibensulfuron, bensulfuron, benazolin, propham, buthan, thiuron, buthan, benazolin, buthan, benazolin, buthan, benazolin, thiuron, thifenbenazolin, thiuron, thifenbenazolin, thiuron, thifenbenazolin, thiuron, thifenbencarb, thiuron, thifenbencarb, thiuron, thifenbencarb, thiuron, thifenbencarb, Thiobencarb, merthiolane, diclofop, triallate, penoxsulam, pyributicarb, dichlorfon, edifenphos, ethiofen, prosulfocarb, clenbuterol, prosulfocarb, dichotomene, thiobencarb, promethazine, Isopolinate, Methiobencarb, 2, 4-d butyl ester, 2 methyl 4-sodium chloride, 2, 4-d isooctyl ester, 2 methyl 4-chloroisooctyl ester, 2, 4-d sodium salt, 2, 4-d dimethylamine salt, 2 methyl 4-chloroethyl thioester, 2 methyl 4 chloride, 2, 4-d propionic acid, 2, 4-d propionate, 2, 4-d butyric acid, 2 methyl 4-chloropropionic acid, 2 methyl 4-chlorobutyric acid, 2,4, 5-d nasal discharge, 2,4, 5-d propionic acid, 2,4, 5-d butyric acid, 2 methyl 4-chloropropionic acid, 2 methyl 4-d propionic acid, 2-d propionic acid, 2-cloroprionic acid, triclocarb, triclopyr, clorac, aminodiclofenac, metocloprofenac, diclofop-methyl, fluazifop-p-butyl, haloxyfop-methyl, haloxyfop-p-butyl, quizalofop-ethyl, quizalofop-p-ethyl, fenoxaprop-p-ethyl, propaquizafop-ethyl, fenoxaprop-ethyl, clodinafop-ethyl, benazolin, clodinafop-ethyl, haloxyfop-methyl, benazolin, propalaxyl, butyfen-ethyl, chloroethafloxacin, aminofluanid, benazolin, dichlofop-ethyl, methamphetalin, propamocarb-ethyl, benfop-methyl, thiophosphine, pirimiphos-methyl, benfop-ethyl, benazolin, benfop-methyl, imax-methyl, mefenofos, mefenap-ethyl, mefenoxaprop-p-ethyl, mefenofos, mefenoxaprop-p-ethyl, mefenoxaprop-p-ethyl, mefenoxaprop-p-ethyl, mefenoxaprop-p-ethyl, mefenofos, mefenap-p-ethyl, mefenoxaprop-p-ethyl, mefenoxaprop-p-ethyl, mefenoxaprop-p-ethyl, mefenozide, mefenoxaprop-ethyl, mefenoxaprop-p-ethyl, mefenoxaprop-p-ethyl, mefenoxaprop-p-, Imazamox ammonium salt, imazapic acid, imazamethabenz ester, fluroxypyr, clopyralid, picloram, triclopyr, dithiopyr, haloxydine, triclopyril, thiazopyr, fluridone, aminopyralid, diflufenzopyr, butoxyethyl triclopyr, Clodinate, sethoxydim, clethodim, cycloxydim, clethodim, topramezone, Buthidazole, metribuzin, hexazinone, metamitron, metribuzin, amitridione, Amibuzin, bromoxynil, octanoyl ioxynil, dichlobenitrile, pyraclonil, hydroxybensulam, Iodobonil, flumetsulam, penoxsulam, clofenapyr, pyraclonil, pyraflufen-ethyl, pyraoxystrobin, flumetsulam, pyraclonil, pyraoxystrobin, isoxathion, pyraclonil, pyraoxystrobin, pyraclonil, pyraclostrobin, propyzachlor, pyraclostrobin, flufenapyr-ethyl, pyraclostrobin, flufenapyr-ethyl, pyraclostrobin, Pyriftalid, pyriminobac-methyl, pyrithiobac-methyl, benzobicylon, mesotrione, sulcotrione, Tembotrione, Tefuryltrione, Bicyclopyrone, ketodradox, isoxaflutole, isoxaclomazone, fenoxasulfofone, methiozoline, isopyrafen, pyraflufen, pyrazote, difenzoquat, pyrazoxazole, pyroxaflutole, pyroxsulam, pyraclofos, pyraclonil, amicarbazone, carfentrazone, flumiclone, sulfentrazone, bencarane, bisphenomezone, butafenacil, isoxaflutole, cyclam, triclopyr, fluroxypyr, flumethazine, parnaprox, flumiclone, flumethol, carfentrazone, carzone, carfentrazone, tebufenozide, tebufadix, tebufenozide, tebufalin, tebufenozide, tebufalin, fluazifop-methyl, pyriminostrobin, bromopicrin, didaphylm, pyridaben, Pyridafol, quinclorac, chloroquine, bentazon, pyridate, oxaziclomefone, benazolin, clomazone, isoprox, isoproxypyrim, propyribac, cumylfen, clomazone, sodium chlorate, thatch, trichloroacetic acid, monochloroacetic acid, hexachloroacetone, tetrafluoropropionic acid, mequat, bromophenol oxime, triazasulam, imazazole, flurtamone, mesotrione, ethofumesate, pyrimethanil, clodinafop-methyl, clodinium, pyributaine, benfurazolin, meton, metamitron, metolachlor, dichlorvofen, triclopyr, aloac, Dietmquat, Etpronil, ipriflam, iprimazam, iprodione, Trizopyr, Thiaclonifen, chlorpyrifos, pyradifquat, chlorpyrifos, propiram, pyradifurone, pyradifon, pyradifurone, pyrazone, thion, pyrazone, thiothifluzone, pyrazone, thiothifluzone, thion, thiothifluzone, thion, thiobenflurazolidone, thion, thifluzone, thion, thifluzone, thidiazuron, thidiaz, Clomazone, fenclorim, cloquintocet-mexyl, mefenpyr-diethyl, DOWFAUC, UBH-509, D489, LS 82-556, KPP-300, NC-324, NC-330, KH-218, DPX-N8189, SC-0744, DOWCO535, DK-8910, V-53482, PP-600, MBH-001, KIH-9201, ET-751, KIH-6127 and KIH-2023.
The herbicidal composition further comprises a safener selected from one or more of isoxadifen, p-cymene sulfonamide, mefenpyr-diethyl, cloquintocet-mexyl, gibberellic acid, furilazole and N- (2-methoxybenzoyl) -4- [ (methylaminocarbonyl) amino ] benzenesulfonamide.
The compositions of the invention can be applied by spraying to the foliage of the plants to be treated, i.e. to the weeds, in particular to surfaces which are harmful or susceptible to infestation by weeds which are harmful to crop growth.
When the herbicidal composition of the present invention is applied, an unexpected synergistic effect is obtained, and the herbicidal activity is more remarkable than the expected sum of the activities using individual herbicides, and the activities of the individual herbicides alone. The synergistic effect is manifested by reduced application rates, a broader spectrum of weed control, and a faster and longer lasting herbicidal action, which are desirable in the practice of weed control. These new compositions are clearly superior to existing herbicides in terms of the properties described.
The herbicidal composition of the present invention also has the following advantages:
(1) the composition is environment-friendly, is easy to degrade in the environment, and is suitable for various crop fields.
(2) The weeding composition disclosed by the invention is low in cost and convenient to use, and has great economic and social benefits when popularized and applied.
(3) Compared with the prior art, the weeding composition can prevent and kill non-resistant gramineous weeds, and can prevent and kill cockspur grass, black nightshade and moleplant seed which can resist an ALS inhibitor, and the like, and is an effective scheme for weed resistance management.
Detailed Description
The following examples are not intended to limit the invention, but merely to illustrate how the invention may be carried out. These examples show particularly significant effectiveness against certain weeds. Examples are as follows:
A) example- -compounding of A with pyridate
Emulsifiable concentrate formulation
The formula comprises the following components:
example 1) 4% of A + 16% of pyridate + 20% of cyclohexanone + 7% of calcium dodecylbenzenesulfonate + 7% of nonylphenol polyoxyethylene ether +150# of aromatic solvent oil
Example 2) 6% A + 24% pyridate + 25% cyclopentanone + 5% calcium dodecylbenzenesulfonate + 10% phenethylphenol polyoxyethylene ether +100# aromatic solvent oil
The processing equipment of the missible oil comprises the following steps: vacuum pump, batching cauldron, storage tank.
The processing process of the missible oil comprises the following steps: putting all the materials into a batching kettle, stirring and dissolving until the materials are completely transparent, transferring the materials to a storage tank for filling after the materials are qualified in a test.
Microemulsion formulations
The formula comprises the following components:
example 3) 4% of A + 16% of pyridate + 20% of cyclohexanone + 10% of isooctanol + 8% of sodium cis-dioctyl sulfonate + 8% of polyoxyethylene phenyl ether + 4% of polyoxyethylene phenyl ether formaldehyde resin condensate + water to complement
Example 4) 3% of A + 12% of pyridate + 15% of cyclohexanone + 8% of isooctanol + 6% of sodium cis-dioctyl sulfonate + 10% of polyoxyethylene phenyl ether + 4% of polyoxyethylene phenyl ether formaldehyde resin condensate + water to complement
The microemulsion processing equipment comprises the following steps: vacuum pump, batching cauldron, storage tank.
The processing process of the microemulsion comprises the following steps: putting the original drug and the solvent into a batching kettle, stirring and dissolving until the solution is completely transparent, then adding the emulsifier, stirring uniformly, finally adding water, stirring until the solution is completely transparent, transferring to a storage tank for filling after the assay is qualified.
Aqueous emulsion preparation
The formula comprises the following components:
example 5) 3% A + 12% pyridate + 15% cyclohexanone + 15% 200# solvent oil + 3% phenethyl phenol polyoxyethylene ether phosphate triethanolamine salt + 4% phenethyl phenol polyoxyethylene ether + 3% castor oil polyoxyethylene ether + 0.2% xanthan gum + 3% ethylene glycol + water to make up
Example 6) 5% A + 20% pyridate + 25% cyclohexanone + 15% 200# solvent oil + 3% phenethylphenol polyoxyethylene ether phosphate triethanolamine salt + 5% phenethylphenol polyoxyethylene ether + 3% castor oil polyoxyethylene ether + 0.1% xanthan gum + 3% ethylene glycol + water to make up
The processing equipment of the emulsion in water comprises: a vacuum pump, a batching kettle, a storage tank and a shearing kettle.
The processing process of the emulsion in water comprises the following steps: putting the original drug and the solvent into a material mixing kettle, stirring and dissolving the original drug and the solvent until the original drug and the solvent are completely transparent, then adding the emulsifier, uniformly stirring the mixture to form an oil phase, then pumping the glycol, the defoamer and the water into a shearing kettle, finally slowly pumping the oil phase into the shearing kettle in a shearing state, continuously shearing the materials for 1 hour after all the materials are pumped, transferring the materials to a storage tank for filling after the materials are qualified in testing.
Aqueous suspension formulation
The formula comprises the following components:
example 7) 4.5% a + 18% pyridate + 3% polycarboxylate dispersant + 3% EO-PO block polyether + 2% fatty alcohol polyoxyethylene ether + 0.2% xanthan gum + 1.5% magnesium aluminium silicate + 5% glycerol + water to make up.
Example 8) 6% a + 24% pyridate + 4% polycarboxylate dispersant + 4% EO-PO block polyether + 2% fatty alcohol polyoxyethylene ether + 0.15% xanthan gum + 1.5% magnesium aluminium silicate + 5% glycerol + water to make up.
The processing equipment of the aqueous suspending agent comprises: mixing kettles, colloid mills, sand mills, shearing machines and the like.
The processing process of the aqueous suspending agent comprises the following steps: putting all materials into a mixing kettle, stirring and mixing, passing through a colloid mill, then entering a sand mill for three-stage sand milling, finally uniformly shearing in a shearing machine, and transferring to a storage tank for filling after the test is qualified.
Dispersible oil suspension formulation
The formula comprises the following components:
example 9) 4% A + 16% pyridate + 5% calcium dodecylbenzenesulfonate + 7% fatty acid polyoxyethylene ether + 4% castor oil polyoxyethylene ether + 2.5% organobentonite + 2.0% fumed silica + 10% 150# mineral spirits + methyl oleate.
Example 10) 6.5% a + 26% pyridate + 4% calcium dodecylbenzenesulfonate + 7% fatty acid polyoxyethylene ether + 4% castor oil polyoxyethylene ether + 2.5% organobentonite + 1.5% fumed silica + 20% 200# mineral spirits + methyl oleate.
Example 11) 8% A + 32% pyridate + 6% calcium dodecylbenzenesulfonate + 6% nonylphenol ethoxylate + 4% castor oil ethoxylate + 2.5% organobentonite + 40% 200# solvent oil + methyl oleate.
Example 12) 5% A + 20% pyridate + 6% calcium dodecylbenzenesulfonate + 7% fatty acid polyoxyethylene ether + 4% castor oil polyoxyethylene ether + 0.5% organobentonite +100# mineral spirits.
The processing equipment of the dispersible oil suspending agent comprises the following steps: mixing kettles, colloid mills, sand mills, shearing machines and the like.
The processing process of the dispersible oil suspending agent comprises the following steps: putting all materials into a mixing kettle, stirring and mixing, passing through a colloid mill, then entering a sand mill for three-stage sand milling, finally uniformly shearing in a shearing machine, and transferring to a storage tank for filling after the test is qualified.
Wettable powder formulation
The formula comprises the following components:
example 13) 4% A + 16% pyridate + 10% naphthalenesulfonate dispersant + 5% nekal + 25% precipitated silica + diatomaceous earth
Example 14) 6% A + 24% pyridate + 10% naphthalenesulfonate dispersant + 5% sodium dodecylsulfate + 30% precipitated silica + calcined Kaolin to complement
The processing equipment of the wettable powder comprises: mechanical disintegrator, jet mill.
The processing process of the wettable powder comprises the following steps: putting the raw medicines, the auxiliary agents, the white carbon black, the kaolin and the like into a mechanical pulverizer, then passing through an airflow pulverizer, and sampling, testing and qualifying for later use.
Water dispersible granule formulation
The formula comprises the following components:
example 15) 3% a + 12% pyridate + 10% polycarboxylate dispersant + 6% nekal + 1% disintegrant polyvinyl alcohol + 25% precipitated silica + filler diatomaceous earth.
Example 16) 5% of A + 20% of pyridate + 15% of polycarboxylate dispersant + 4% of sodium lauryl sulfate + 1% of disintegrant polyvinyl alcohol + 30% of precipitated silica + filler calcined kaolin.
The water dispersible granule processing equipment comprises: jet mills, coulter mixers, basket granulators, drying ovens, screening machines, and the like.
The processing process of the water dispersible granule comprises the following steps: the materials are uniformly mixed, crushed by airflow, added with water, kneaded, granulated, dried and finally screened to obtain the finished product.
B) Example A compounding with Cyclopyrimate
Emulsifiable concentrate formulation
The formula comprises the following components:
example 17) 3% A + 3% cyclopyromate + 10% N-methylpyrrolidone + 7% calcium dodecylbenzenesulfonate + 7% fatty alcohol-polyoxyethylene ether + 3% phenethylphenol-polyoxyethylene ether-formaldehyde resin condensate +150# aromatic solvent oil is sufficient
Example 18) 5% A + 5% cycloprozole + 20% cyclohexanone + 7% calcium dodecylbenzenesulfonate + 8% nonylphenol polyoxyethylene ether + 2.5% phenethylphenol polyoxyethylene ether formaldehyde resin condensate +150# aromatic solvent oil
The processing equipment of the missible oil comprises the following steps: vacuum pump, batching cauldron, storage tank.
The processing process of the missible oil comprises the following steps: putting all the materials into a batching kettle, stirring and dissolving until the materials are completely transparent, transferring the materials to a storage tank for filling after the materials are qualified in a test.
Microemulsion formulations
The formula comprises the following components:
example 19) 5% A + 5% cycloprozole + 25% cyclohexanone + 10% n-octanol + 8% sodium di-sec-octylmaleate sulfonate + 8% polyoxyethylene styrene ether + 2% polyoxyethylene styrene ether formaldehyde resin condensate + Water to complement
Example 20) 8% A + 8% cycloprozole + 25% cyclopentanone + 8% isooctanol + 6% sodium di-sec-octylmaleate sulfonate + 10% polyoxyethylene phenethyl ether + 4% polyoxyethylene phenethyl phenol formaldehyde resin condensate + water to complement
The microemulsion processing equipment comprises the following steps: vacuum pump, batching cauldron, storage tank.
The processing process of the microemulsion comprises the following steps: putting the original drug and the solvent into a batching kettle, stirring and dissolving until the solution is completely transparent, then adding the emulsifier, stirring uniformly, finally adding water, stirring until the solution is completely transparent, transferring to a storage tank for filling after the assay is qualified.
Aqueous emulsion preparation
The formula comprises the following components:
example 21) 4% A + 4% cycloprozole + 15% cyclohexanone + 15% 200# solvent oil + 3% phenethylphenol polyoxyethylene ether phosphate triethanolamine salt + 3% phenethylphenol polyoxyethylene ether + 3% castor oil polyoxyethylene ether + 0.2% xanthan gum + 3% ethylene glycol + water to make up
Example 22) 5% A + 5% cycloprozole + 25% cyclohexanone + 15% 200# solvent oil + 3% phenethylphenol polyoxyethylene ether phosphate triethanolamine salt + 4% phenethylphenol polyoxyethylene ether + 3% castor oil polyoxyethylene ether + 0.1% xanthan gum + 3% ethylene glycol + water to make up
The processing equipment of the emulsion in water comprises: a vacuum pump, a batching kettle, a storage tank and a shearing kettle.
The processing process of the aqueous emulsion comprises the following steps: putting the original drug and the solvent into a material mixing kettle, stirring and dissolving the original drug and the solvent until the original drug and the solvent are completely transparent, then adding the emulsifier, uniformly stirring the mixture to form an oil phase, then pumping the glycol, the defoamer and the water into a shearing kettle, finally slowly pumping the oil phase into the shearing kettle in a shearing state, continuously shearing the materials for 1 hour after all the materials are pumped, transferring the materials to a storage tank for filling after the materials are qualified in testing.
Aqueous suspension formulations
The formula comprises the following components:
example 23) 4.5% A + 4.5% cycloprozoate + 3% polycarboxylate dispersant + 3% EO-PO block polyether + 2% fatty alcohol polyoxyethylene ether + 0.2% xanthan gum + 1.5% magnesium aluminium silicate + 5% glycerol + water to make up.
The processing equipment of the aqueous suspending agent comprises: mixing kettles, colloid mills, sand mills, shearing machines and the like.
The processing process of the aqueous suspending agent comprises the following steps: putting all materials into a mixing kettle, stirring and mixing, passing through a colloid mill, then entering a sand mill for three-stage sand milling, finally uniformly shearing in a shearing machine, and transferring to a storage tank for filling after the test is qualified.
Dispersible oil suspension formulation
The formula comprises the following components:
example 24) 4% A + 4% cycloprozole + 5% calcium dodecylbenzenesulfonate + 7% nonylphenol ethoxylate + 4% castor oil ethoxylate + 3.0% organobentonite + 2.5% fumed silica + methyl oleate.
Example 25) 6% A + 6% cycloprozole + 4% calcium dodecylbenzene sulfonate + 7% fatty acid polyoxyethylene ether + 4% castor oil polyoxyethylene ether + 2.8% organobentonite + 1.5% fumed silica + 5% 200# mineral spirits + methyl oleate.
Example 26) 8% A + 8% cycloprozole + 6% calcium dodecylbenzenesulfonate + 6% fatty alcohol-polyoxyethylene ether + 4% castor oil-polyoxyethylene ether + 2.5% organobentonite + 5% 200# mineral spirits + methyl oleate.
Example 27) 12% A + 12% cycloprozole + 6% calcium dodecylbenzenesulfonate + 7% fatty acid polyoxyethylene ether + 4% castor oil polyoxyethylene ether + 1.5% organobentonite + 10% 150# solvent oil + methyl oleate.
The processing equipment of the dispersible oil suspending agent comprises the following steps: mixing kettle, colloid mill, sand mill, shearing machine, etc.
The processing process of the dispersible oil suspending agent comprises the following steps: putting all materials into a mixing kettle, stirring and mixing, passing through a colloid mill, then entering a sand mill for three-stage sand milling, finally uniformly shearing in a shearing machine, and transferring to a storage tank for filling after the test is qualified.
Wettable powder formulation
The formula comprises the following components:
example 28) 10% A + 10% cycloprozole + 10% naphthalenesulfonate dispersant + 4% nekal + 15% precipitated silica + diatomaceous earth
Example 29) 15% A + 15% cycloprozole + 10% lignosulfonate dispersant + 5% sodium lauryl sulfate + 20% precipitated silica + calcined kaolin to complement
The processing equipment of the wettable powder comprises: mechanical disintegrator, jet mill.
The processing process of the wettable powder comprises the following steps: putting the raw medicines, the auxiliary agents, the white carbon black, the kaolin and the like into a mechanical pulverizer, then passing through an airflow pulverizer, and sampling, testing and qualifying for later use.
Water dispersible granule formulation
The formula comprises the following components:
example 30) 12% a + 12% cyclopyromate + 10% polycarboxylate dispersant + 6% nekal + 1% disintegrant polyvinyl alcohol + 15% precipitated silica + filler diatomaceous earth.
Example 31) 20% a + 20% cycloprozole + 15% polycarboxylate dispersant + 4% sodium lauryl sulfate + 1% disintegrant polyvinyl alcohol + 20% precipitated silica + filler calcined kaolin.
The water dispersible granule processing equipment comprises: jet mills, coulter mixers, basket granulators, drying ovens, screening machines, and the like.
The processing process of the water dispersible granule comprises the following steps: the materials are uniformly mixed, crushed by airflow, added with water, kneaded, granulated, dried and finally screened to obtain the finished product.
C) Test of drug efficacy
Spraying treatment of stems and leaves after seedling:
1) test conditions
1.1) test target
Echinochloa crusgalli (Echinochloa crusgalli) is collected from paddy fields in Changsha prefecture in Hunan, Echinochloa crusgalli (Stapf) Koss) is collected from Hulongjiang tiger forest city, Euphorbia lathyri (Leptochloa chinensis) is collected from Huangmei county in Hubei, and Solanum nigrum (Solanum nigrum L.) is collected from Shandong yellow island region, the above weeds are cultivated by pot culture, 180 х 140mm plastic nutrition pots are placed in enamel trays, surface soil (4/5) which is air-dried and sieved from farmlands is filled, the soil humidity is controlled at 20% in the initial stage, and the weed seeds with uniform and full seeds are selected, soaked in warm water at 25 ℃ for 6 hours, accelerated to germinate in a biochemical incubator (28 ℃) to ensure that the just exposed white weed seeds are uniformly placed on the surface of the soil, and then covered with soil with 0.5-1cm according to the large and small particle size.
1.2) culture conditions
The method is carried out in a controllable sunlight greenhouse, the temperature is 20-30 ℃, the natural illumination is carried out, and the relative humidity is 57-72%.
The soil type is loam, the organic matter content is 1.63%, the pH value is 7.1, the alkaline hydrolysis nitrogen is 84.3mg/kg, the quick-acting phosphorus is 38.5mg/kg, and the quick-acting potassium is 82.1 mg/kg.
1.3), instrumentation
3WP-2000 model walking spray tower, Minn Jing agricultural machinery research institute of agricultural department. Ten thousandth electronic balance type GA10 (germany); ZDR2000 intelligent data recorder (hangzhou ze large instruments ltd); SPX type intelligent biochemical incubator (Ningbo Jiangnan Instrument factory).
2) Design of experiments
2.1), reagents
2.1.1) test Agents
The desired active ingredient B was purchased from a reagent company and A was produced by this company.
The raw medicines are all diluted by using an emulsifier Tween-80 aqueous solution with the content of 0.1 percent and taking acetone as a solvent.
2.2) test treatment
2.2.1), dose setting
When determining the ratio or content of the component A and the component B, the main use purpose of the formula is also considered according to the action characteristics of the two medicaments and the measurement of toxicity and the like. On the basis of preliminary experiments, A, B active ingredients are respectively used singly and mixed in different amounts. Water without drug, containing the same solvent and emulsifier was used as a blank.
2.2.2) test repetition
Each treatment was repeated 4 times, 3 pots each time, and 20 weed seeds were sown per pot for a total of 60 plants per treatment.
2.3) treatment method
2.3.1), treatment time and number of times
The test was performed 1 time in total. And (3) thinning when 3 leaves of the weeds are in the 1-heart stage, keeping 15 weeds in each pot, keeping 45 weeds in each treatment, then continuously culturing until the barnyard grass, the rice barnyard grass and the moleplant seeds are in the 4-leaf 1-heart stage, and treating the solanum nigrum in the 6-7 leaf stage.
2.3.2), devices and methods of use
Uniformly placing the cultured test material on a 0.5m area2Spraying stem and leaf with 3WP-2000 model walking spraying tower in 30 kg/ha amount. The spraying pressure is 0.3 MPa. And after all the liquid medicine is sprayed, closing the air valve, opening the spraying tower door after 30 seconds, and taking out the nutrition pot. Then the air valve is opened, 50mL of clean water is sprayed, and the liquid spraying pipe is cleaned.
3) Test method
The potting method is adopted. The weed cultivation is carried out according to 1.1 and the standard herbicide for indoor bioassay of pesticides. The application method is 2.3.2, and stem and leaf treatment method is adopted. After treatment, the cells were transferred to a greenhouse for conventional culture, and a 1-2cm water layer was maintained throughout the experiment.
4) Data investigation and statistical analysis
4.1) investigation method
The complete survival weed seedlings are cut off along the soil surface by a blade by adopting an absolute number survey method, and the fresh weight of the weeds is weighed by an analytical balance. For the weeds that have died, the fresh weight is zero.
4.2), investigation time and number of surveys
The investigation was conducted 20 days after the treatment, and the total number of the investigations was 1.
4.3), statistical analysis of data
The theoretical fresh weight inhibition rate (E0 ═ X + Y-X Y/100) of each treatment mixed combination is calculated by a Gowing method, and then compared with the actually measured inhibition rate (E), the combined action type of the two mixed combinations on the weeds is evaluated, and when the E-E0 value is more than 10 percent, the effect is synergistic, when the E-E0 value is less than-10 percent, the effect is antagonistic, and when the E-E0 value is between-10 percent and 10 percent, the effect is additive. And the optimal proportion is determined according to factors such as actual control effect, characteristics of the herbicide, balance of the formula and the like.
Wherein X is the fresh weight inhibition rate when the dosage of the active component A is P; y is the fresh weight inhibition rate of the active component B when the dosage is Q.
The statistical results are shown in tables 1-26, wherein the test materials of solanum nigrum (6-7 leaf stage), moleplant seed (4 leaves 1 heart stage), barnyard grass (4 leaves 1 heart stage) and barnyard grass (4 leaves 1 heart stage) stem leaves are subjected to spray treatment, and the fresh weight control effect is counted 7 days after the test.
TABLE 1 evaluation of the actual control and combination of Black nightshade when blended with pyridate (Gowing)
Figure BDA0001389781420000121
TABLE 2 evaluation of the actual control and combination of weeds with pyridate mixtures (Gowing)
Figure BDA0001389781420000122
Figure BDA0001389781420000131
TABLE 3 evaluation of the actual control and combination of weeds in the Mitsubishi weed control (Gowing)
Figure BDA0001389781420000132
TABLE 4 evaluation of the actual control and combination of weeds in the Mitsubishi weed control (Gowing)
Figure BDA0001389781420000133
TABLE 5 evaluation of actual control and combination of weeds with pyridate combinations (Gowing)
Figure BDA0001389781420000134
TABLE 6 evaluation of actual control and combination of weeds with pyridate combinations (Gowing)
Figure BDA0001389781420000135
Figure BDA0001389781420000141
TABLE 7 evaluation of actual control and combination of weeds with pyridate combinations (Gowing)
Figure BDA0001389781420000142
TABLE 8 evaluation of actual control and combination of weeds with pyridate combinations (Gowing)
Figure BDA0001389781420000143
TABLE 9 evaluation of the actual control and combination of weeds in the Mitsubishi weed control (Gowing)
Figure BDA0001389781420000144
Figure BDA0001389781420000151
TABLE 10 evaluation of actual control and combination of weeds with pyridate combinations (Gowing)
Figure BDA0001389781420000152
TABLE 11 evaluation of actual control and combination of Black nightshade when blended with pyridate (Gowing)
Figure BDA0001389781420000153
TABLE 12 evaluation of the actual control and combination of the combination of Black nightshade and pyridaben (Gowing)
Figure BDA0001389781420000154
TABLE 13 evaluation of actual control and combination of Black nightshade when blended with pyridate (Gowing)
Figure BDA0001389781420000155
Figure BDA0001389781420000161
TABLE 14 evaluation of the actual control and combination of the combination of Black nightshade and pyridaben (Gowing)
Figure BDA0001389781420000162
TABLE 15 evaluation of actual control and combination of Black nightshade when blended with pyridate (Gowing)
Figure BDA0001389781420000163
TABLE 16 evaluation of the actual control and combination of Solanum nigrum by compounding with cycloprominate (Gowing)
Figure BDA0001389781420000164
TABLE 17 evaluation of actual control and Combined action of weed by blending with cyclopromidate (Gowing)
Figure BDA0001389781420000165
TABLE 18 evaluation of actual control and Combined action of weed by compounding with cyclopromidate (Gowing)
Figure BDA0001389781420000171
TABLE 19A evaluation of the actual control and Combined action of weed species paired with cyclopyrmate (Gowing)
Figure BDA0001389781420000172
TABLE 20 evaluation of actual control and Combined action of weed by compounding with cyclopromidate (Gowing)
Figure BDA0001389781420000173
TABLE 21 actual control and Combined action evaluation (Gowing) of weeds paired with cycloprominate
Figure BDA0001389781420000174
Figure BDA0001389781420000181
TABLE 22 evaluation of actual control and Combined action of weed by compounding with cyclopromidate (Gowing)
Figure BDA0001389781420000182
TABLE 23 evaluation of actual control and Combined action of Solanum nigrum by compounding with cycloprominate (Gowing)
Figure BDA0001389781420000183
TABLE 24 evaluation of actual control and Combined action of Solanum nigrum when blended with cycloprominate (Gowing)
Figure BDA0001389781420000184
TABLE 25 evaluation of actual control and Combined action of Solanum nigrum by blending with Cyclopyrimorate (Gowing)
Figure BDA0001389781420000191
TABLE 26 evaluation of the actual control and combination of Solanum nigrum by compounding with cycloprominate (Gowing)
Figure BDA0001389781420000192
D) Demonstration of field
The herbicidal compositions prepared in examples 1) to 31) were used for controlling weeds in paddy fields.
An exemplary promotional test was conducted in 2016 at 4 test sites in the long-sand early rice region of Hunan.
The test method comprises the following steps: after 3 leaves and 1 heart of the rice and 3-4 leaves of weeds, a manual sprayer is used for adding 30 kg of water per 667m 2The stem leaf spray is adopted for uniform spraying, the specific test medicament and dosage are shown in tables 5 and 6, the area of a cell is 50 square meters, and each treatment is repeated for 4 times. The control effect was examined 45 days after application of the composition shown in tables 5 and 6.
Figure BDA0001389781420000193
TABLE 5 field demonstration of Effect of the Compound composition with pyridate
Figure BDA0001389781420000194
Figure BDA0001389781420000201
TABLE 6 demonstration of field Effect of combinations of Cyclopyrimate and composition
Figure BDA0001389781420000202
Figure BDA0001389781420000211
Through a large number of tests and explorations, the composition is unexpectedly found to be used for preventing and removing gramineous weeds in paddy fields after seedlings, has a surprising and unexpected synergistic effect, particularly has a particularly obvious synergistic effect on barnyard grass, moleplant seeds and other gramineous weeds, cyperaceae such as cyperus rotundus and other cyperaceae, monochoria vaginalis, eclipta prostrata and other broadleaf weeds, has a more remarkable synergistic effect under a low dose, can reduce the dosage, is safe for paddy, reduces the pollution to the environment, is reasonably compounded, reduces the agricultural cost, is efficient on ALS and ACCase inhibitor resistant weeds, and has a good application prospect. Meanwhile, tests show that the herbicide composition shows good selectivity and excellent synergistic effect on lawns and crops such as wheat fields, corn fields, soybeans, cotton, vegetables, bluegrass, tall fescue, zoysia japonica and the like, and can be developed into herbicide mixtures with wide market values.

Claims (12)

1. A weeding composition containing triazophone and pyridazine compounds is characterized by comprising an active ingredient A and an active ingredient B which have herbicidally effective amounts, wherein the active ingredient A is the triazophone, the active ingredient B is the pyridazine compounds selected from pyridate or cyclopropyrolate, and the weight ratio of the A to the B is 1:100-100: 1.
2. The herbicidal composition comprising triazophone and pyridazine compounds according to claim 1 wherein the weight ratio of A to B is 1:80 to 80: 1.
3. The herbicidal composition comprising triazophone and pyridazine compounds according to claim 2 wherein the weight ratio of A to B is 1:50 to 50: 1.
4. The herbicidal composition comprising triazophone and pyridazine compounds according to claim 3 wherein the weight ratio of A to B is 1:20 to 20: 1.
5. The herbicidal composition comprising triazophone and pyridazine compounds according to claim 4 wherein the weight ratio of A to B is 1:10 to 10: 1.
6. The herbicidal composition comprising triazophone and pyridazine compounds according to claim 5 wherein the weight ratio of A to B is 1:5 to 5: 1.
7. The weeding composition containing triazophone and pyridazine compounds according to any one of claims 1-6, wherein A and B are present in the weeding composition in an amount of 1-95% by mass.
8. The weeding composition containing mesotrione and pyridazine compound according to claim 7, wherein the weight percentage of A and B in the weeding composition is 10-80% of the total weight.
9. The weeding composition containing triazophone and pyridazine compounds according to any one of claims 1-6, further comprising a carrier and a surfactant.
10. The weeding composition containing the triazophone and the pyridazine compound according to any one of claims 1-6, wherein the weeding composition is dispersible oil suspension, water suspension, suspoemulsion, wettable powder, emulsifiable concentrate, water dispersible granule, aqueous emulsion or microemulsion.
11. The herbicidal composition comprising triazophone and pyridazine compounds according to any one of claims 1-6, further comprising a safener selected from one or more of isoxadifen, p-cymene sulfonamide, mefenpyr, cloquintocet, gibberellic acid, furazolidone and N- (2-2 methoxybenzoyl) -4- [ (methylaminocarbonyl) amino ] benzenesulfonamide.
12. Use of the herbicidal composition comprising triazophone and a pyridazine compound according to any one of claims 1 to 11 for controlling harmful weeds in crops of crops.
CN201710744235.5A 2017-08-25 2017-08-25 Weeding composition containing triazophorbine and pyridazine compound and application thereof Active CN107372551B (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN201710744235.5A CN107372551B (en) 2017-08-25 2017-08-25 Weeding composition containing triazophorbine and pyridazine compound and application thereof
PCT/CN2017/112010 WO2019037313A1 (en) 2017-08-25 2017-11-21 Herbicidal composition containing triazole sulcotrione and application thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710744235.5A CN107372551B (en) 2017-08-25 2017-08-25 Weeding composition containing triazophorbine and pyridazine compound and application thereof

Publications (2)

Publication Number Publication Date
CN107372551A CN107372551A (en) 2017-11-24
CN107372551B true CN107372551B (en) 2022-06-28

Family

ID=60347180

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710744235.5A Active CN107372551B (en) 2017-08-25 2017-08-25 Weeding composition containing triazophorbine and pyridazine compound and application thereof

Country Status (1)

Country Link
CN (1) CN107372551B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109479888A (en) * 2018-12-19 2019-03-19 青岛清原化合物有限公司 Ternary weeding composition and its application comprising cyclopyrimorate
CN114304165B (en) * 2020-09-30 2023-07-07 青岛清原化合物有限公司 Binary weeding composition and application thereof
CN115088725A (en) * 2021-08-16 2022-09-23 吉林省八达农药有限公司 Weeding composition and preparation method thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105503728A (en) * 2015-12-31 2016-04-20 青岛清原化合物有限公司 Pyrazole compounds or salts thereof and preparation method thereof, and weedicide composition and application thereof

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105503728A (en) * 2015-12-31 2016-04-20 青岛清原化合物有限公司 Pyrazole compounds or salts thereof and preparation method thereof, and weedicide composition and application thereof

Also Published As

Publication number Publication date
CN107372551A (en) 2017-11-24

Similar Documents

Publication Publication Date Title
CN113057169B (en) Herbicidal composition containing bicyclopyrone and application thereof
CN107568230B (en) Weeding composition containing triazasulam and application thereof
CN107836452B (en) Weeding composition containing triazasulam and application thereof
WO2020019430A1 (en) Ternary herbicidal composition containing hppd inhibitor herbicide and use thereof
CN113016811A (en) Weeding composition containing topramezone and application thereof
CN109497075B (en) Ternary herbicidal composition containing trifludimoxazin and application thereof
CN107517978B (en) Ternary weeding composition containing triazophos-clomazone and anilofos and application thereof
CN106070309B (en) Complex herbicidal composition and its application method containing polybenzobisoxazole humulone
CN114431236B (en) Ternary herbicidal compositions comprising carboxylic acid derivative substituted oxyiminoaryl compounds and uses thereof
CN109964943B (en) Herbicidal compositions comprising pyrimidinyloximes and their use
CN116250539A (en) Ternary weeding composition containing fenpyrazamine and application thereof
CN110946144B (en) Herbicidal composition containing clomazone and application thereof
CN107372551B (en) Weeding composition containing triazophorbine and pyridazine compound and application thereof
CN105994354B (en) Complex herbicidal composition and its application method containing ring pyrrole fluorine humulone
CN112741097B (en) Herbicidal compositions comprising N- (1, 3, 4-oxadiazol-2-yl) arylcarboxamides and their use
CN112841202B (en) Herbicidal composition containing pyrimidine benzyl carboxylate compound and ALS inhibitor and application thereof
CN107897191B (en) Weeding composition containing topramezone and application thereof
WO2020215604A1 (en) Herbicidal composition comprising trifluoromethyl pyridazinol compound and application thereof
CN106508913B (en) Herbicide composition containing triazophoron and triafamone and application thereof
CN107484765B (en) Synergistic weeding composition containing topramezone and topramezone
CN107372525B (en) Weeding composition containing triazasulam and application thereof
CN106561665B (en) Wheat field weeding composition and application thereof
WO2019228215A1 (en) Ternary herbicidal composition and application thereof
WO2020124531A1 (en) Ternary herbicidal composition containing cyclopyrimorate and application thereof
CN110870481A (en) Herbicidal composition containing heterocyclic amide compound and application thereof

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
GR01 Patent grant
GR01 Patent grant