The present disclosure provides a herbicide composition and a preparation method and an application method thereof, and relates to the technical field of herbicides. The herbicide composition includes pinoxaden and a cyclic lactone compound. The cyclic lactone compound is five-membered cyclic lactone and/or six-membered cyclic lactone. The herbicide composition solves the technical problems of poor chemical stability and precipitation due to crystallization at low temperature of existing pinoxaden emulsifiable concentrate formulations. In the herbicide composition, the cyclic lactone compound is used in combination with the pinoxaden, such that not only the solubility of the pinoxaden is improved, but also a chemical stabilization effect of the pinoxaden is effectively improved, and the problems of precipitation due to crystallization at low temperature and chemical stability of the pinoxaden emulsifiable concentrate formulations are solved.

The present disclosure provides a herbicide composition and a preparation method and an application method thereof, and relates to the technical field of herbicides. The herbicide composition includes pinoxaden and a cyclic lactone compound. The cyclic lactone compound is five-membered cyclic lactone and/or six-membered cyclic lactone. The herbicide composition solves the technical problems of poor chemical stability and precipitation due to crystallization at low temperature of existing pinoxaden emulsifiable concentrate formulations. In the herbicide composition, the cyclic lactone compound is used in combination with the pinoxaden, such that not only the solubility of the pinoxaden is improved, but also a chemical stabilization effect of the pinoxaden is effectively improved, and the problems of precipitation due to crystallization at low temperature and chemical stability of the pinoxaden emulsifiable concentrate formulations are solved.

The present application discloses herbicidal compositions containing a first herbicide beflubutamid, or an optically enriched form thereof, and a second herbicide selected from WSSA Group 15 herbicides, WSSA Group 13 herbicides, WSSA Group 27 herbicides, WSSA Group 9 herbicides, WSSA Group 10 herbicides, WSSA Group 22 herbicides, WSSA Group 7 herbicides, WSSA Group 3 herbicides, WSSA Group 14 triazolinone herbicides, WSSA Group 1 cyclohexanedione herbicides, WSSA Group 2 imida-zolinone herbicides, WSSA Group 14 N-phenylphthalimide herbicides, WSSA Group 14 diphenylether herbicides, WSSA Group 14 pyrimidinedione herbicides, WSSA Group 5 1,2,4-triazine herbicides and herbicides selected from metamifop, atrazine, fenoxaprop-P-ethyl, 2,4-D (2,4-dichlorophenoxyacetic acid), florasulam, halosulfuron-methyl and prosulfocarb. The application also discloses a method of controlling undesired vegetation in a crop by applying to the locus of such vegetation a herbicidally effective amount of a herbicidal composition.

Provided are pesticide application kits comprising a liquid formulation comprising a glucosinolate concentrate, an active myrsoinase enzyme complex, and a water soluble polyol. Further included in the kits are instructions for the addition of water to form a diluted formulation, and application of the diluted formulation to a pest.

Provided are pesticide application kits comprising a liquid formulation comprising a glucosinolate concentrate, an active myrsoinase enzyme complex, and a water soluble polyol. Further included in the kits are instructions for the addition of water to form a diluted formulation, and application of the diluted formulation to a pest.

The present invention relates to novel sulfoperoxycarboxylic acid compounds, and methods for making and using them. The sulfoperoxycarboxylic compounds of the invention are storage stable, water soluble and have low to no odor. Further, the compounds of the present invention can be formed from non-petroleum based renewable materials. The compounds of the present invention can be used as antimicrobials, and bleaching agents. The compounds of the present invention are also suitable for use as coupling agents.

The present invention relates to novel sulfoperoxycarboxylic acid compounds, and methods for making and using them. The sulfoperoxycarboxylic compounds of the invention are storage stable, water soluble and have low to no odor. Further, the compounds of the present invention can be formed from non-petroleum based renewable materials. The compounds of the present invention can be used as antimicrobials, and bleaching agents. The compounds of the present invention are also suitable for use as coupling agents.

The present invention relates to novel sulfoperoxycarboxylic acid compounds, and methods for making and using them. The sulfoperoxycarboxylic compounds of the invention are storage stable, water soluble and have low to no odor. Further, the compounds of the present invention can be formed from non-petroleum based renewable materials. The compounds of the present invention can be used as antimicrobials, and bleaching agents. The compounds of the present invention are also suitable for use as coupling agents.

The present invention relates to novel sulfoperoxycarboxylic acid compounds, and methods for making and using them. The sulfoperoxycarboxylic compounds of the invention are storage stable, water soluble and have low to no odor. Further, the compounds of the present invention can be formed from non-petroleum based renewable materials. The compounds of the present invention can be used as antimicrobials, and bleaching agents. The compounds of the present invention are also suitable for use as coupling agents.

The present invention provides a production method of an antimicrobial cellulosic fiber which includes the following steps: A, preparing a reactive antibacterial compound: B, preparing an antimicrobial cellulosic fiber: B1, chemical immobilization: B2, processing the structural body by a metal promoter or a heat treatment to stabilize it, and obtain an antimicrobial cellulosic fiber. In the present invention, a reactive antibacterial compound is prepared by a reaction of a reactive compound and an antibacterial agent, the reactive antibacterial compound is chemically immobilized to the cellulosic fiber through the chemical bonds between the reactive compound and the cellulosic fiber, so that the structure of the cellulosic fiber is more stable.