WO2003026429A1 - Herbicide compositions comprising suspension concentrate with glyphosate acid, methods of preparation, and methods of use - Google Patents

Herbicide compositions comprising suspension concentrate with glyphosate acid, methods of preparation, and methods of use Download PDF

Info

Publication number
WO2003026429A1
WO2003026429A1 PCT/US2002/008952 US0208952W WO03026429A1 WO 2003026429 A1 WO2003026429 A1 WO 2003026429A1 US 0208952 W US0208952 W US 0208952W WO 03026429 A1 WO03026429 A1 WO 03026429A1
Authority
WO
WIPO (PCT)
Prior art keywords
acid
suspension concentrate
glyphosate
surfactant
acidifying agent
Prior art date
Application number
PCT/US2002/008952
Other languages
French (fr)
Inventor
Anthony E. Herold
Richard A. Beardmore
Scott K. Parrish
Original Assignee
Platte Chemical Co.
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=27502307&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2003026429(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Platte Chemical Co. filed Critical Platte Chemical Co.
Priority to BR0212876-4A priority Critical patent/BR0212876A/en
Priority to EP02799541A priority patent/EP1432316A1/en
Priority to CA2462127A priority patent/CA2462127C/en
Publication of WO2003026429A1 publication Critical patent/WO2003026429A1/en

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
    • A01N37/00Biocides, 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
    • A01N37/36Biocides, 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
    • A01N37/38Biocides, 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
    • 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
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • 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
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A01N25/04Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
    • 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
    • A01N37/00Biocides, 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
    • A01N37/36Biocides, 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
    • A01N37/38Biocides, 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
    • A01N37/40Biocides, 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
    • 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
    • A01N39/00Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
    • A01N39/02Aryloxy-carboxylic acids; Derivatives 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
    • A01N39/00Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
    • A01N39/02Aryloxy-carboxylic acids; Derivatives thereof
    • A01N39/04Aryloxy-acetic acids; Derivatives 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • 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
    • A01N43/501,3-Diazoles; Hydrogenated 1,3-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
    • 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
    • A01N43/601,4-Diazines; Hydrogenated 1,4-diazines
    • 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
    • A01N57/00Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/18Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
    • A01N57/20Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
    • 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
    • A01N59/00Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/16Heavy metals; Compounds thereof
    • A01N59/20Copper

Definitions

  • HERBICIDE COMPOSITIONS COMPRISING SUSPENSION CONCENTRATE WITH GLYPHOSATE ACID
  • Herbicide Compositions Comprising Imidazolinone Acid, Methods of Preparation, 10 and Methods of Use, having Attorney Docket No. UAP0008/US, filed February 28, 2002.
  • the invention relates to compositions comprising suspension concentrates 15 and other herbicide compositions that contain glyphosate acid, methods of preparing such suspension concentrates and herbicide compositions, and methods of using each.
  • herbicide compositions include a very large variety of active herbicide compounds.
  • Such herbicide compositions can be prepared from different types of precursor compositions, and can be commercially available and used in a variety of different types of compositions, including, for example, compositions referred to as wettable powders, water dispersible granules, granules,
  • compositions 25 aqueous solutions, water soluble powders, emulsifiable concentrates, oil-based flowables, concentrated emulsions, suspo-emulsions, emulsions, suspensions, suspension concentrates, mixtures, dispersions, and microemulsions, as well as others. Any of these different types of compositions may have different advantages or disadvantages relating to factors such as the mode of application and
  • Examples of just a few available active herbicide compounds include those of the general class known as phenoxy herbicides, e.g., 2,4-dichlorophenoxyacetic acid (known as 2,4-D), MCPA acid, MCPP acid; those of the general class known as pyridine herbicides, (e.g., triclopyr, fluoroxypyr); those of the general class of benzoic acid herbicides, (e.g., dicamba acid); those of the general class of aryloxy phenoxy propionic acid herbicides, (e.g., fluzafop acid and quizolofop acid); water-insoluble diphenyl ether type herbicides (e.g., oxyfluorfen or acifluorfen); glyphosate compounds (N-(phosphonomethyl)glycine), e.g., in the acid form, referred to as glyphosate acid, or in a salt form such as the IPA salt form; imidizole herbicide compounds
  • Active herbicide ingredients such as these and others can be prepared from and used in the form of solid and liquid compositions including, as mentioned above, different forms of emulsions, suspensions, suspension concentrates, mixtures, dispersions, microemulsions, etc., and derivatives thereof such as diluted solutions or solutions including other added ingredients such as additional herbicides.
  • this compound is understood to be available in a variety of chemically different forms including glyphosate acid and glyphosate salts.
  • glyphosate compounds are described as being useful in herbicide compositions in their salt form, or as glyphosate acid, in combination with specific surfactants as a water-soluble free-flowing solid formulation. See, for example, United States patent numbers 5,118,338, 5,668,085, and 5,994,271.
  • the salts of glyphosate e.g., ammonium, sodium, isopropylammonium, and trimesium, are considered to be very soluble in water, while the acid form is not.
  • New forms of effective herbicide compositions are always desirable, especially those that can show advantages in processing, application, environmental profile (e.g., volatility), or efficacy.
  • the invention relates to suspension concentrates that include the herbicide compound glyphosate acid, in the acid form, and derivatives and uses of those suspension concentrates.
  • the suspension concentrates can be used in their suspension concentrate form to control plant growth, or can be used to prepare derivative herbicide compositions for application to control plant growth.
  • the suspension concentrate can be combined with an acidifying agent, e.g., in a tank mix procedure or otherwise, to form a herbicide application composition, and can optionally be further combined with other ingredients such as an additional, different active herbicide compound.
  • Preferred herbicide application compositions can have a pH below about 2.6 or 2.3, or otherwise below the pKa of glyphosate acid compound.
  • the suspension concentrate has been found to be easily and efficiently producible with the use of one or more other ingredients such as surfactants (wetting agents), dispersants, thickeners, etc., one or more of which optionally in combination with one or more of mixing, agitation, and milling, etc., can allow glyphosate acid particles to be suspended and/or dispersed in water to form a suspension concentrate.
  • surfactants wetting agents
  • dispersants thickeners, etc.
  • the use of a herbicide composition containing glyphosate in the acid form provides efficiency because the acid form does not need to be converted to the glyphosate salt form during processing or prior to application, as is often done with the glyphosate herbicide compound (because the salt forms are more soluble in water).
  • the suspension concentrate of the invention including the glyphosate acid herbicide in its glyphosate acid form, is simple and economical to produce, and can be efficiently distributed, prepared, and applied without taking steps to convert the glyphosate herbicide out of its acid form.
  • the invention can also advantageously provide improved efficacy of the glyphosate acid herbicide compound, especially when used in combination with acidifying agents.
  • the glyphosate acid suspension concentrates have other benefits when compared to other herbicide formulations such as the absence of dust; reduction of toxicity or flammability, etc.; they do not require organic solvents; they can exhibit increased efficacy, for example due to lower particle size; they benefit from a low packing volume as compared to other forms of herbicides such as powers; and the suspension concentrates are relatively easy to handle.
  • an aspect of the invention relates to a suspension concentrate comprising glyphosate acid particles suspended in water and surfactant selected from the group consisting of cationic surfactant, anionic surfactant, and mixtures thereof.
  • suspension concentrates comprising glyphosate acid and short chain alcohol ethoxylate nonionic surfactant, e.g., having a short chain branched or linear alkyl having from 3 to 23 or fewer carbon atoms.
  • Yet another aspect of the invention relates to a herbicide composition
  • a herbicide composition comprising a suspension concentrate comprising glyphosate acid, and acidifying agent other than sulfuric acid in an amount so the pH of the herbicide composition is below the pKa of glyphosate acid.
  • Another aspect of the invention relates to a herbicide composition
  • a herbicide composition comprising a suspension concentrate comprising glyphosate acid.
  • the herbicide composition also includes acidifying agent other than sulfuric acid, in an amount so the pH of the herbicide composition is below the pKa of glyphosate acid.
  • Another aspect of the invention relates to a method of applying a herbicide composition, the method comprising: preparing a herbicide composition comprising a suspension concentrate comprising glyphosate acid, and acidifying agent other than sulfuric acid, the acidifying agent being included in an amount so that the pH of the herbicide composition is below the pKa of glyphosate acid; and applying the herbicide composition to control plant growth.
  • Still another aspect of the invention relates to a method of preparing a suspension concentrate comprising glyphosate acid.
  • the method comprises: combining glyphosate acid particles with water and surfactant selected from anionic surfactant, cationic surfactant, short chain alcohol ethoxylate nonionic surfactant, and mixtures thereof; and mixing or agitating the water, glyphosate acid particles, and surfactant to produce a suspension concentrate.
  • Still a further aspect of the invention relates to a method of preparing a suspension concentrate comprising glyphosate acid.
  • the method comprises: combining glyphosate acid particles with water, surfactant, and dispersant; wet milling the mixture of glyphosate acid particles, water, surfactant, and dispersant, to reduce the size of glyphosate acid particles to a size that can be suspended in the water, surfactant, and dispersant; and using a high speed mixer to mix the water, glyphosate acid particles, surfactant, and dispersant, to produce a suspension concentrate comprising the glyphosate acid particles.
  • Yet another aspect of the invention relates to a method of preparing a herbicide composition comprising glyphosate acid.
  • the method comprises preparing a suspension concentrate composition by a method comprising: combining glyphosate acid particles with water and one or more of surfactant and dispersant; mixing or agitating the water, glyphosate acid particles, and one or more of surfactant and dispersant, to produce a suspension concentrate containing the glyphosate acid particles; and combining the suspension concentrate composition with acidifying agent other than sulfuric acid.
  • Glyphosate N-(phosphonomethyl)glycine compounds (or "glyphosate”), and chemical derivatives thereof, are a known type of active herbicide compound. Glyphosate is generally considered a broad spectrum, post-emergent, systemic herbicide effective for the control of many annual and perennial grasses and broadleaf weeds, in addition to many tree and wooden brush species both in cropland and noncrop sites. Glyphosate is available in the acid form, referred to as glyphosate acid, and is also available and more commonly used for herbicide application in it's various salt forms, such as its isopropylamine (IPA) salt form.
  • IPA isopropylamine
  • Glyphosate is sold as the isopropylamine salt under the trade name Roundup®.
  • the invention relates to herbicide compositions that include glyphosate acid, i.e., glyphosate (N-(phosphonomethyl)glycine), in the acid form.
  • glyphosate acid i.e., glyphosate (N-(phosphonomethyl)glycine
  • the term "herbicide composition” refers to compositions that include a herbicide compound, specifically here, glyphosate acid.
  • Herbicide compositions include the described suspension concentrates and derivatives thereof.
  • Glyphosate acid is generally considered to be an insoluble active herbicide compound.
  • glyphosate acid can be soluble in water or acidic water only up to a few weight percent, meaning that approximately 100 grams of an aqueous solution can dissolve only approximately a couple of grams of glyphosate acid, e.g., approximately 1 gram, or one weight percent.
  • the glyphosate compound (N- (phosphonomethyl)glycine) includes 4 acidic protons which are removed at pKa t of 0.8 (1 st phosphonic), pKa 2 2.3 or 2.6 (carboxylate), pKa 3 6.0 (2 nd phosphonic), and pKa 11.0 (amine).
  • the pKa 2 is specifically meant, because this is the pKa that relates to the conversion of the glyphosate compound to and from the protonated and deprotonated carboxylic acid form, which is generally considered to be the "acid" form of the glyphosate herbicide compound. See, for example, http://www.soils.wisc.edu/virtual_museum/glyphosate/glyphosate_tx.html, which is part of the Virtual Museum of Minerals and Molecules, originally released 25 Dec, 1999, and last modified 31, Dec, 2000.
  • Glyphosate acid is commercially available, generally in the form of a granular, solid, powder form or as a wet cake, for example from Dow Chemical Co., under the tradename Glyphosate WC. These materials are sold in the form of solid glyphosate acid particles having an average size (diameter) in the range from about 5 to about 18 microns. According to the invention, glyphosate acid is incorporated into a suspension concentrate.
  • composition concentrate means a composition also sometimes referred to as an "aqueous flowable” or a “water- based flowable” composition, which compositions are known in the herbicide art and include or consist of particles of a generally insoluble solid active herbicide compound in suspension (preferably concentrated suspension) in water.
  • the suspension concentrates described herein can be produced with particles of glyphosate acid by suspending and preferably dispersing the particles in water with the assistance of other ingredients such as conventional dispersants, surfactants (wetting agents), and other optional ingredients.
  • the glyphosate acid should be in the form of particles that exhibit physical characteristics such as size, shape, surface features, etc., that will allow the glyphosate acid particles to be suspended in water as described.
  • the particle size range can vary depending on factors such as the other ingredients used to prepare the suspension concentrate and their respective amounts, but exemplary particles may be in the size range below about 10 microns, for example in the range from about 4 or 5 to about 7 or 8 microns.
  • the suspension concentrate includes water in a useful amount, such as an amount that, in combination with one or more other ingredients described herein (e.g., such as surfactant and/or dispersant) will allow suspension and preferably dispersion of the glyphosate acid particles.
  • a useful amount such as an amount that, in combination with one or more other ingredients described herein (e.g., such as surfactant and/or dispersant) will allow suspension and preferably dispersion of the glyphosate acid particles.
  • Relative amounts of water and the other ingredients used to prepare a suspension concentrate can be any amounts that produce a useful herbicide composition in the form of a suspension concentrate.
  • Relative amounts of different ingredients (water, glyphosate acid, surfactant, etc.) in any particular composition can depend on the intended application (including the plant to be controlled or the crop to be protected), the mode of application (e.g., field or aerial spraying or application from a hand-held spray applicator, or other technique), the method of any preparation from a suspension concentrate to a herbicide application composition, the amounts and identities of other ingredients added to the suspension concentrate, etc.
  • Useful amounts of water in a suspension concentrate may be, for example, in the range from about 20 to about 60 weight percent water based on the total weight of the suspension concentrate, such as from about 30 to about 50 weight percent water in a suspension concentrate.
  • a wetting agent (also referred to herein as "surfactant”), can be used to facilitate suspending the glyphosate acid particles in a suspension concentrate.
  • Surfactants can lower the surface tension of the water, helping to replace air on the surface of particles of the glyphosate acid with water, thereby suspending the particles.
  • new particle surfaces are created by mechanical breakdown of solid glyphosate particles. The surfactant adsorbs onto the particle surfaces to give rise to fluidity of the suspension.
  • surfactants are known and commercially available, including such different classes as cationic surfactants, anionic surfactants, non- ionic surfactants, ionic surfactants, and amphoteric surfactants, etc.
  • the surfactant can be a surfactant or combination of surfactants useful to suspend particles of glyphosate acid. Examples of some preferred surfactants include cationic, certain non-ionic surfactants, and anionic surfactants, either alone or in combinations (e.g., blends of cationic and nonionic surfactants).
  • surfactants include non-ionic linear or branched alcohol ethoxylate surfactants, anionic phosphoric acid ester surfactants (sometimes referred to as "phosphate ester” surfactants), and cationic ethoxylated tallow amine surfactants.
  • An example of useful surfactant would include nonionic wetting agents such as Surfonic LI 2-6, from Huntsman.
  • Other examples of commercially available surfactants of these general classes include the following:
  • anionic surfactant is a surface-active molecule in which an active portion of a lipophilic portion of the molecule forms a negative ion (i.e., anion) when placed in aqueous solution.
  • exemplary anionic surfactants include phosphoric acid ester surfactants (sometimes referred to as "phosphate ester” surfactants), sodium alkyl naphthalene sulfonate surfactants, and ethoxylated tristyrylphenol phosphate salts.
  • Exemplary sodium alkyl naphthalene sulfonate surfactants include sodium butyl naphthalene sulfonate, sodium di-n-butyl naphthalene sulfonate, sodium diisopropyl naphthalene sulfonate, sodium dimethyl naphthalene sulfonate, and mixtures thereof.
  • Sodium butyl naphthalene sulfonate is commercially available, for example, under the trade name "MORWET B" from Witco/Crompton, Greenwich, CT.
  • Sodium di-n-butyl naphthalene sulfonate is commercially available, for example, under the trade name "MORWET DB” from Witco/Crompton, Greenwich, CT.
  • Sodium diisopropyl naphthalene sulfonate is commercially available, for example, under the trade name "MORWET IP” from Witco/Crompton, Greenwich, CT.
  • Sodium dimethyl naphthalene sulfonate surfactant is commercially available, for example, under the trade name "SELLOGEN HR" from Henkle Corp., Cincinnati, OH.
  • An exemplary ethoxylated tristyrylphenol phosphate potassium salt surfactant is commercially available, for example, under the trade name "SOPROPHOR FLK" from Rhodia, Cranbury, NJ.
  • a nonionic surfactant is a surface-active molecule that does not contain ionizable polar end groups but does contain hydrophilic and lipophilic portions.
  • Exemplary nonionic surfactants include polyoxyethylene alkylether or alkenylether surfactants.
  • Nonionic surfactant used to prepare a suspension concentrate as described herein may include long or short chain alcohol ethoxylate surfactant. The alcohol ethoxylate surfactant may be branched or linear.
  • An example of a useful nonionic polyoxyalkylene surfactant includes alcohol ethoxylate having the general formula:
  • R may be "long” or “short” chain and “branched” or “linear” alkyl.
  • R preferably can be a "short chain” branched or linear alcohol, meaning that it can have from about 3 to 23 or fewer carbon atoms.
  • x can preferably be in the range from about 2 to 5, preferably from about 2 to 4 (e.g., 2 or 3, for a polyoxyethylene or polyoxypropylene, respectively) and y can preferably be in the in the range from 5 to 25.
  • Examples of useful short chain nonionic polyoxyalkylenes include linear alcohol polyoxyethylenes having the general formula:
  • CH 3 (C 2 H 4 ) m is a short chain linear alkyl having from about 3 to 23 or fewer carbon atoms (i.e., m can be in the range from about 1 to 11 carbon atoms), and n is in the range from about 5 to 25.
  • Another example is short chain nonionic polyoxypropylenes having the general formula:
  • CH 3 (C 2 H 4 ) m is a short chain linear alkyl having from about 3 to 23 or fewer carbon atoms (i.e., m can be in the range from about 1 to 11 carbon atoms), and n can preferably be in the range from about 5 to 25.
  • Exemplary short chain linear alcohol ethoxylate surfactant are commercially available, for example, under the trade names "SURFONIC LI 2-6" from Huntsman, Austin, TX, "SURFONIC L24-7” from Huntsman, Austin, Texas, “TERGITOL 15-S-7", “TERGITOL 24-L-60”, “ALPHONIC 1012-60”,
  • exemplary surfactants include polyethylene glycol, fatty acid ethoxylates, phosphate esters, octyl phenol ethoxylates, and nonyl phenol ethoxylates.
  • polyethylene glycol surfactants are commercially available, for example, under the trade names "ADEKA PEG” from Asahi Denka Kogyo, Tokyo, Japan.
  • Useful fatty acid ethoxylate surfactants are commercially available, for example, under the trade names "NINEX MT-610", “NINEX MT-615", and “NINEX MT-630" from Stepan, Northfield, IL.
  • Useful phosphate ester surfactants are commercially available, for example, under the trade names “STEPFAC 8180", “STEPFAC 8181”, and “STEPFAC 8182” from Stepan.
  • Useful octyl phenol ethoxylate surfactants are commercially available, for example, under the trade name “MAKON OP-9" from Stepan, Northfield, IL.
  • Useful nonyl phenol ethoxylate surfactants are commercially available, for example, under the trade names "MAKON 4", “MAKON 6", “MAKON 8", “MAKON 10", “MAKON 12", and “MAKON 14" from Stepan, Northfield, IL.
  • a cationic surfactant is a surface-active molecule in which an active portion of a lipophilic portion of the molecule forms a positive ion (i.e., cation) when placed in aqueous solution.
  • exemplary cationic surfactant includes ethoxylated tallow amine.
  • the amount of surfactant (“surfactant” refers to one or a combination of surfactants) can be any amount that will allow the preparation of a suspension concentrate. Useful amounts of surfactant will be apparent to the skilled artisan based on this overall description, with exemplary amounts being below about 20 percent by weight surfactant based on the total weight of suspension concentrate, such as in the range from about 0.1 or 1 to about 10 or 15 weight percent surfactant based on the total weight of the suspension concentrate with a particularly preferred range being from 0.5 to 3 weight percent.
  • a dispersant can also be useful to facilitate preparation of a suspension concentrate containing glyphosate acid particles.
  • a dispersant can stabilize and maintain a separation between the suspended particles, which otherwise may have a tendency to flocculate due to attractive forces.
  • Dispersants can provide repulsive forces to balance the tendency to flocculate.
  • An example of a useful type of dispersant is a nonionic dispersant such as Tersperse 4892 from Huntsman. Other examples of dispersants are listed in the table above.
  • the amount of dispersant can be any amount that will allow the preparation of a suspension concentrate, and that may help to stabilize a suspension concentrate, e.g., by preventing flocculation. Useful amounts may depend on the type of dispersant and the composition of the suspension concentrate, as will be apparent to the skilled artisan. Exemplary amounts of dispersant can be below about 10 or 8 percent by weight dispersant based on the total weight of the suspension concentrate, with preferred amounts being from about 2 to about 6 weight percent dispersant based on the total weight of the suspension concentrate. Other ingredients, additives, or adjuvants can also be included in the suspension concentrate, as will be appreciated by those skilled in the relevant arts.
  • an antifreeze may be useful, such as propylene glycol or other low molecular weight alcohols or polyols, in an amount to reduce the freezing point of the suspension concentrate.
  • the amount of the antifreeze can be any amount that is useful, as will be understood by the skilled artisan.
  • Exemplary amounts of antifreeze can be below about 20 weight percent based on the total weight of the suspension concentrate, for example from 1 to about 15 weight percent, or from about 5 to about 10 weight percent.
  • Thickeners can be included in the suspension concentrate to provide gravitational stabilization by increasing viscosity.
  • Useful thickeners include chemical compounds and polymeric materials that will be known to and understood by the skilled artisan, and include, generally, natural and synthetic starches, gums, and other types of chemical compounds that will increase the viscosity of a solution.
  • Thickening agents are well known in the chemical and polymer arts, and include, inter alia, polyacrylamides, cellulosic resins and functionalized cellulosic resins, polyacrylic acids, polyethylene oxides, and the like.
  • a useful amount of thickener will result in increased viscosity and stability, without causing viscosity build that would be excessive for application of the composition as a herbicide. Amounts below about 5 or 10 weight percent, based on the total weight of the suspension concentrate, may generally be useful. Preferred amounts may be less 0.5 weight percent for gums or cellulose resins.
  • Another ingredient in a suspension concentrate can be an antifoaming agent. Antifoaming agents are well understood in the chemical and herbicide arts, and a variety of useful examples are commercially available. Antifoam agents are substances such as silicones, organic phosphates, and alcohols, which inhibit the formation of bubbles in a liquid by reducing surface tension.
  • antifoam agent a 10% silicone in water
  • SAG 10 a 10% silicone in water
  • the amount of antifoaming agent used in a suspension concentrate will also be apparent to the skilled artisan, with typical amounts being less than 1 percent by weight, e.g., less than 0.5 percent by weight.
  • Other useful additives or adjuvants to the suspension concentrate may include other surfactants, antimicrobial agents, anticorrosion agents, and other ingredients that; will be understood to be useful, in amounts that will also be understood.
  • Surfactants having functions of wetting, spreading, or penetrating, preferably to improve efficacy of a herbicide composition may also be added to the formulation or can be added when a tank mix is made for application.
  • Organic solvents may be included in the suspension concentrate if desired, but are generally not used or needed.
  • the ingredients can be combined by known methods, including mixing, agitating, and dispersing, and, if needed or otherwise desired, milling of the glyphosate acid particles, to produce a suspension concentrate. Any of the mixing, milling, agitating, dispersing, or combining steps can be done in any order, such as milling the glyphosate acid particles and adding the milled particles to water and other ingredients, or by adding the particles to water and other ingredients followed by wet milling.
  • One exemplary method of producing a suspension concentrate starts with glyphosate acid particles in the form of a wet cake or dry (granular, powder) acid, generally having a relatively large particle size (e.g., greater than about 10 microns).
  • the wet cake or dry particles of that size can be mixed or dispersed into a liquid. This can be done, for example, by combining the glyphosate acid particles with water and other ingredients with agitation or mixing to disperse the particles.
  • the glyphosate acid particles can be added to water and one or more of surfactant, dispersant, antifreeze, and antifoam, and mixed using a highspeed mixer to disperse the glyphosate acid particles.
  • the mixture of glyphosate acid, water, and other ingredients can be further processed toward a suspension concentrate by methods that will process the glyphosate acid particles into a form that allows suspension of the particles in water in the form of a suspension concentrate, for instance by reducing the size of the particles in the presence of a useful surfactant.
  • a processing step can be to reduce the size of glyphosate acid particles to a size that will allow the particles, in combination with one or more of the other ingredients described herein such as surfactant and/or dispersant, to be maintained in a stable suspension concentrate composition.
  • An exemplary method of reducing the size of the glyphosate acid particles is by using milling techniques, e.g., what is referred to as "wet milling.”
  • a typical such average particle size can be below about 10 microns, for example in the range from about 4 to about 8 microns or from about 5 to about 7 microns.
  • Any method of reducing particle size may be useful, such as by using an attrition mill, ball mill, sand mill, or other milling process.
  • the solution containing the suspended glyphosate acid particles can be further combined with a thickener, by mixing the thickener into the solution.
  • the suspension concentrate can preferably be stable in the form of a suspension concentrate for a useful period, meaning that the suspension concentrate composition does not settle or otherwise transform out of the suspension concentrate form, and maintains the form of a suspension concentrate, for a useful amount of time.
  • Useful periods of stability can depend on timing, e.g., between preparation, further processing of, and use (application) of the suspension concentrate, which time periods may vary greatly based on convenience, preference, inherent stability of the suspension, or other factors.
  • suspension concentrate or a derivative form of the suspension concentrate can be applied in a short or very short period of time after preparation, longer-term stability is not required.
  • Exemplary suspension concentrates of the invention have been found to be stable at approximately room temperature and in substantially undisturbed and un-agitated environments for periods in excess of 6 or 12 months. Longer or shorter periods would also be useful.
  • the suspension concentrate can be applied directly to a field or plant to control undesired plant growth, or can be combined with other ingredients to form a derivative herbicide composition for application which can be applied to a field or plant, e.g., as a "herbicide application composition” to control undesired plant growth.
  • "herbicide application composition” refers to a herbicide composition having a concentration of herbicide compound (here, glyphosate acid) that would normally be applied to a field or plant to control undesired plant growth, as opposed, for example, to compositions having higher concentrations of herbicide compound that sometimes occur in preparation, storage, shipping, or sale of a herbicide composition. It is noted that suspension concentrate compositions as described herein are capable of controlling plant growth if applied directly to a plant.
  • herbicide application compositions include any herbicide composition having such a specific concentration of glyphosate acid for application, e.g., to a field, and specifically include suspension concentrates and derivatives prepared by combining the suspension concentrate with one or more of water, acidifying agent, another herbicide, or other ingredients, as will be described in more detail below.
  • Additional ingredients can be added to the suspension concentrate to produce a derivative herbicide composition or herbicide application composition. These added ingredients may be useful in the herbicide composition for purposes of dilution, stability, pH adjustment, anti-foaming, or to otherwise facilitate application or increase efficacy. These other ingredients may be added to the suspension concentrate or derivative herbicide composition at any time and in any order, as desired or convenient. Exemplary additional ingredients include water, antifoaming agents, acidifying agents, anticorrosion agents, or additional active herbicide compounds, such as described, for example, in Applicants' copending U.S. Patent Application entitled "Herbicide Compositions Comprising Imidazolinone Acid, Methods of Preparation, and Methods of Use," having Attorney Docket No. UAP0008/US/2, U.S. Serial No. , filed on even date herewith.
  • a preferred embodiment of a herbicide composition of the invention comprising or prepared from a suspension concentrate comprising glyphosate acid, can further include acidifying agent, particularly an acidifying agent that improves the efficacy of the herbicide composition.
  • acidifying agent particularly an acidifying agent that improves the efficacy of the herbicide composition. Examples of a certain type of acidifying agent are described in United States Patent Numbers 4,445,925, 4,994,101,
  • a preferred herbicide application composition can be formulated to include an acidifying agent, and most preferably to include sufficient acidifying agent to exhibit a pH that is below about 2.6, preferably below about 2.3, e.g., below the pKa of glyphosate acid.
  • a neutral (acid) molecule can have an easier time penetrating a cuticle on a plant, compared to a charged (salt) molecule.
  • an acidifying agent and a low pH of a herbicide composition can have a damaging effect on a plant's surface, thereby letting more herbicide penetrate the surface.
  • the neutral acid molecule can be less susceptible to de-activation by hard water.
  • a variety of different acidifying agents can be useful with the herbicide compositions of the invention.
  • the particular acidifying agent chosen and the amount used can be based on factors including the intended use or application of the herbicide composition (including the identity of the target undesirable plant growth and any nearby desirable plant growth) the method of application, physical and chemical properties of the herbicide application composition, and others.
  • the acidifying agent may be any of a variety of suitable organic or inorganic acids, of any useful strength or concentration, that can be added to a suspension concentrate or a derivative thereof, preferably without causing substantial or undue negative effects such as reaction with an ingredient of the suspension concentrate such as the glyphosate acid, precipitation, etc. It will be understood that an acidifying agent can be in a concentrated or diluted form, as necessary or desirable.
  • Non-limiting examples of acidifying agents include acids such as sulfuric acid, phosphoric acid, hydrochloric acid, nitric acid, acetic acid (e.g., "glacial” acidic acid), perchloric acid, polyphosphoric acid, acidic adducts such as the sulfuric acid adducts described in United States Patent Number 5,288,692 (Young), especially the adduct of sulfuric acid and urea, or any other acidifying agent that can be used to affect the pH of a herbicide composition, especially to prepare a herbicide composition including glyphosate acid and having a pH below the pKa of glyphosate acid.
  • acids such as sulfuric acid, phosphoric acid, hydrochloric acid, nitric acid, acetic acid (e.g., "glacial” acidic acid), perchloric acid, polyphosphoric acid, acidic adducts such as the sulfuric acid adducts described in United States Patent Number 5,288,692 (Young), especially
  • X is chalcogen
  • Ri, R 2 and R 3 is independently selected from hydrogen and organic radicals.
  • amide encompasses all compounds of formula (1 ) regardless of the chalcogen.
  • the molar ratio of amide to acid is usually in the range of about 1/4 to less than 2 so that at least some of the acid is present as the monoamide-acid adduct.
  • Ri, R 2 , and R 3 are organic radicals, they may be cyclic or acyclic, straight or branched chained, and can contain one or more heteroatoms such as sulfur, nitrogen, oxygen, phosphorus and the like. Further, Ri, R 2 and R 3 can contain one or more substituents such as thiol, hydroxy, nitro, amino, nitrile, amide, ester and halogen groups and others. Such organic radicals may contain aryl groups such as aralkyl and alkaryl groups. Certain preferred organic radicals can be free of olefinic or alkynyl unsaturation and can generally have up to about 20, preferably up to about 10 carbon atoms. Particularly preferred amides include urea, thiourea, formamide, dimethylformamide, biuret, triuret, thioformamide, and combinations of these.
  • the chalcogens are elements of Periodic Group VI-B and include. oxygen, sulfur, selenium, tellurium, and polonium. Oxygen and sulfur can be preferred due to low cost, availability, low toxicity, and chemical activity, and oxygen is the most preferred.
  • a specific example of an adduct according to formula (1) can be the sulfuric acid/urea adduct:
  • useful acidifying agents include various forms of sulfuric acid, phosphoric acid, hydrochloric acid, nitric acid, acetic acid (e.g., "glacial” acidic acid), perchloric acid, polyphosphoric acid, adducts of these, etc.
  • Various such acids are commercially available in different forms and concentrations, such as solids, liquid (aqueous) solutions, concentrated liquid solutions, etc., or can be prepared by one of skill. Any such form of acidifying acid may be useful to reduce the pH of a herbicide composition prepared from or comprising the suspension concentrate, preferably without causing any undue negative affects.
  • the chosen form of acidifying agent may be based on commercial availability, convenience, and the overall desired properties of the herbicide composition, its different ingredients (e.g., the herbicide compound), and its desired method of preparation and use.
  • the amount of acidifying agent added to a suspension concentrate or herbicide application composition can be based on factors including the particular composition and chemistry of the suspension concentrate or herbicide application composition, including the amounts and chemistries of surfactant and herbicide compound; the amount of water; the type of acidifying agent and its chemistry and strength (concentration); the desired pH; etc.
  • Preferred amounts of any particular acidifying agent can be capable of improving the efficacy of the herbicide composition as applied, and particularly preferred amounts will be sufficient to produce an application composition having a pH below 2.3 or 2.6, or otherwise below the pKa of glyphosate acid compound.
  • aqueous acidifying agent such as those listed above can be below about 5 or 10 volume percent, e.g., in the range from about 0.01 to about 4 parts by volume aqueous acidifying agent based on the total by volume of suspension concentrate and acidifying agent. Volumes of acidifying agent outside of this range may also be useful, depending on the composition and strength of the acidifying agent and the desired pH.
  • the herbicide compositions can be used for immediate and long-term, post- emergent control of a large variety of different forms of vegetation.
  • the suspension concentrate could be applied directly to plants for controlling plant growth, although this may include an unnecessarily potent concentration of the glyphosate acid.
  • a suspension concentrate would instead more likely be a product sold commercially as a herbicide concentrate product, which would be a composition that includes a relatively high concentration of glyphosate acid active herbicide compound, as manufactured or packaged for sale, and which may typically be diluted or combined with other ingredients prior to use to form a herbicide application composition.
  • the suspension concentrate could be purchased by distributors or suppliers, or directly by consumers such as farmers, any of which could add optional ingredients such as water, an acidifying agent (e.g., in the form of a solid, powder, or an aqueous solution, etc.), or another type of herbicide formulation or herbicide compound, to the suspension concentrate.
  • the additional ingredients could, for example, be added and mixed in a tank immediately prior to application.
  • the suspension concentrate would typically be diluted with water. A typical dilution would be 1 pint of suspension concentrate in 15 gallons of water for ground application. Another typical dilution would be 1 pint of suspension concentrate in 3-5 gallons of water for application by air.
  • a suspension concentrate could be sold to farming product or nursery dealers, or the like, who could dilute the suspension concentrate with water and/or add other ingredients such as an acidifying agent or other herbicide. This could be particularly convenient if such a dealer normally kept a stock of acidifying agent such as phosphoric acid or sulfuric acid, etc.
  • the suspension concentrate combined with acidifying agent by the dealer could be sold to an end consumer who could use the composition as purchased or who could optionally further dilute the purchased composition or add other ingredients to the purchased composition such as an additional herbicide by tank mixing.
  • the suspension concentrate could be sold directly to end users who could add one or more of the additional ingredients in a tank mixing process.
  • the suspension concentrate could be combined with water or an acidifying agent or both, in a tank, by a farmer, and then applied.
  • the herbicide compositions can be applied for immediate vegetation control by contact killing, by application of a herbicide application composition to plants.
  • herbicide application compositions as described can contain a useful amount of the glyphosate acid active herbicide compound, based on factors of efficacy, safety, application rate, etc.
  • a useful amount of herbicide application composition (containing the useful amount of glyphosate acid) to be applied to a plant or a field, will be readily understood by those of skill, based, e.g., on desired efficacy, safety, application rate, and environmental factors, etc.
  • any specific herbicide application composition will depend on factors known and as described above.
  • certain preferred herbicide application compositions of the invention especially those that include an acidifying agent, and in particular those that also have a reduced pH, e.g., below about 3, 2.6, or 2.3, can be applied at lower dosages or "application rates" (lower amounts of herbicide compound per plant or per acre) relative to other herbicide compositions containing other forms of glyphosate (e.g., the salt form), or not at a reduced pH as described.
  • Examples of dosages ("application rates") of glyphosate acid, especially as included in a herbicide compositions of the described pH, to a field, can be in the range from about 1/100 to about 6 pounds glyphosate acid per acre, with dosages in the range from about 0.03 to 0.5 pounds per acre being particularly preferred. More resistant plants or different field environments may require higher concentrations and/or higher dosage rates.
  • the preparation of herbicide application compositions suitable to apply useful dosages, based on the concentration of herbicide compound in a suspension concentrate, will be understood by one of ordinary skill.
  • the herbicide compositions can, as indicated, be applied using conventional aerial or ground spray techniques in field applications.
  • the herbicide compositions can also be applied by any other useful technique, such as by spot- application to undesired plant growth using a hand-held applicator, or the like.
  • herbicide compositions of the invention have been found to exhibit the additional advantages of being relatively non- volatile.
  • the advantage of non- volatile herbicide compositions are self-evident to those of skill in the herbicide arts.
  • a non- volatile herbicide composition has the advantage of not evolving, or evolving to a reduced degree, through the air, to inadvertently contact desired plant growth. In practical effect, this advantageous property allows the herbicide compositions of the invention to be applied to undesired plant growth in greater strength or in closer proximity to desired above-ground plant growth.
  • Vegetation that can be controlled using the herbicide compositions of the invention include any type of vegetation that is or is known to be controlled by glyphosate or glyphosate acid herbicide compounds.
  • the ingredients of the herbicide compositions e.g., surfactant, dispersant, acidifying agent, etc., can be selected in view of the type of control desired (i.e. pre-emergent or post-emergent) and the type of vegetation to be controlled according to the known attributes of glyphosate compounds, including glyphosate acid.
  • a typical suspension concentrate containing 3 lb glyphosate acid per gallon can be prepared as described herein, from ingredients including:
  • exemplary suspension concentrate formulations may also include a higher amount of surfactant (e.g., 8% by weight or greater) and can have a glyphosate acid concentration of 4 pounds per gallon, as follows:
  • the 8% surfactant provides wetting for the preparation of the suspension concentrate, and upon dilution in water functions as an adjuvant to improve efficacy of the herbicide formulation.
  • ingredients of a suspension concentrate Water 32.45%
  • suspension concentrates of the invention can be used to control plant growth, optionally with an acidifying agent.
  • Rhodofac RS 710 8.0 anionic, phosphate ester surfactant
  • the PCC-1133 microemulsion was made by adding surfactants to a mixing vessel and warming to 130F- 150F. Antifoam and acid were added and mix in until clear, with the 2,4-D acid becoming dissolved in the surfactant, producing a MFC. A microemulsion was formed from the MFC by combining 2 ml MFC with 98 ml water with agitation.
  • the pH of the spray solution of each treatment was measured with a, VWR Scientific model 8005 pH meter.
  • the pH was measured to determine if the acid used or the amount of acid added was sufficient to lower the pH below the pKa of the acid herbicides used.
  • the pKa of 2,4-D acid in the PCC-1133 was measured to be 2.87.
  • the pKa of glyphosate acid in PCC-1168 was measured to be about 2.5 or 2.6.
  • crops were at the following stages: corn - 2 to 3 If, oat - 2 to 3 If, cotton - cotyledon, kochia - 7 If, bean -1st trifoliate, and sunflower - 2 to 4 If.
  • Plants were treated using a greenhouse track sprayer equipped with an 800 IE nozzle and calibrated to deliver 140 L ha-1 at the height of the crop canopy. Each treatment was simultaneously applied to three trays of plants, one for each replicate. After treatment, the plants were left in the head house to dry and then transferred to the greenhouse. Plants in each treatment were evaluated visually for injury 1 day, 1 week, and 2 weeks after treatment.
  • PCC-1168+Polyphosphoric (4%) Following are data that illustrate the efficacy of various herbicide compositions of Experiments 1, 2, and 5.
  • SALVO® is a commercially available product of Platte Chemical Co. containing 5 lb 2,4-D acid equivalent/gallon as 2-ethyl-hexyl ester of 2,4-D
  • SABER® is 2,4-D formulated as a dimethylamine salt (2,4-dichlorophenoxy dimethylamine salt), i.e., is a commercially available product of Platte Chemical Company containing 3.8 lb 2,4-D acid equivalent/gallon as dimethylamine salt.
  • RODEO is a soluble liquid water based formulation of IPA, glyphosate, and water, commercially available from MONSANTO, and was used according to the labeling instructions.
  • RODEO ULTRA is a glyphosate salt herbicide composition commercially available from MONSANTO, and was used according to the labeling instructions.
  • ENGAME is a soluble liquid water based formulation of glyphosate acid, urea, sulfuric acid, and water, commercially available from ENTEK, and was used according to the labeling instructions.
  • ROUNDUP and ROUNDUP ULTRA are commercially available IPA glyphosate salt and surfactant herbicide compositions.
  • AMADS urea and H 2 S0 4 in water
  • LI-136 blend of 50 wt. % 21-0-0 urea liquor and 50 wt percent of 72% phosphoric acid in water.
  • 21-0-0 urea liquor means a liquid that contains 21% by volume urea (nitrogen), 0% by volume phosphate (phosphorous), and 0% by volume potash (potassium).
  • Each of the acids were used as is and combined with the PCC-1133 or PCC-1168 herbicide compositions to form a solution that contains 2 percent or 4 percent by volume of the acid solution, as indicated in the data tables, and such that the pH of the herbicide composition was below the pKa of the particular herbicide compound.
  • the ingredients of the herbicide compositions as applied are listed in the following data tables, and were diluted with water and used at the rates indicated for herbicide ingredients and acidifying agents. .
  • PCC-1174 4 %V/V PCC-1168 0.125 LBAE/A 70.0 60.0 70.0 63.3 76.7
  • NITRIC ACID 4 LB AE/A PCC-1168 .0625 % V/V 0.0 0.0 0.0 10.0 55.0 65.0
  • NITRIC ACID 4 LB AE/A PCC-1168 0.25 % V/V 75.0 70.0 60.0 60.0 80.0 90.0
  • NITRIC ACID 4 LB AE/A PCC-1168 0.5 % V/V 80.0 85.0 60.0 85.0 90.0 98.0
  • NITRIC ACID 4 LB AE/A PCC-1168 .0313 % V/V 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0

Abstract

Described are suspension concentrates that include glyphosate acid, herbicide compositions prepared therefrom, and methods of making and using each.

Description

HERBICIDE COMPOSITIONS COMPRISING SUSPENSION CONCENTRATE WITH GLYPHOSATE ACID
5 This application claims the benefit of U.S. Provisional Application Serial
No. 60/325,289^ U.S. Provisional Application Serial No. 60/325,342, and U.S. Provisional Application Serial No. 60/325,343, all filed September 26, 2001, and the benefit of U.S. Provisional Application Serial No. , entitled
Herbicide Compositions Comprising Imidazolinone Acid, Methods of Preparation, 10 and Methods of Use, having Attorney Docket No. UAP0008/US, filed February 28, 2002.
Field of the Invention
The invention relates to compositions comprising suspension concentrates 15 and other herbicide compositions that contain glyphosate acid, methods of preparing such suspension concentrates and herbicide compositions, and methods of using each.
Background
20 Commercially available herbicide compositions include a very large variety of active herbicide compounds. Such herbicide compositions can be prepared from different types of precursor compositions, and can be commercially available and used in a variety of different types of compositions, including, for example, compositions referred to as wettable powders, water dispersible granules, granules,
25 aqueous solutions, water soluble powders, emulsifiable concentrates, oil-based flowables, concentrated emulsions, suspo-emulsions, emulsions, suspensions, suspension concentrates, mixtures, dispersions, and microemulsions, as well as others. Any of these different types of compositions may have different advantages or disadvantages relating to factors such as the mode of application and
30 the type of active ingredient included in the herbicide composition.
Examples of just a few available active herbicide compounds include those of the general class known as phenoxy herbicides, e.g., 2,4-dichlorophenoxyacetic acid (known as 2,4-D), MCPA acid, MCPP acid; those of the general class known as pyridine herbicides, (e.g., triclopyr, fluoroxypyr); those of the general class of benzoic acid herbicides, (e.g., dicamba acid); those of the general class of aryloxy phenoxy propionic acid herbicides, (e.g., fluzafop acid and quizolofop acid); water-insoluble diphenyl ether type herbicides (e.g., oxyfluorfen or acifluorfen); glyphosate compounds (N-(phosphonomethyl)glycine), e.g., in the acid form, referred to as glyphosate acid, or in a salt form such as the IPA salt form; imidizole herbicide compounds (e.g., imazapyr or imazaquin); as well as others.
Active herbicide ingredients such as these and others can be prepared from and used in the form of solid and liquid compositions including, as mentioned above, different forms of emulsions, suspensions, suspension concentrates, mixtures, dispersions, microemulsions, etc., and derivatives thereof such as diluted solutions or solutions including other added ingredients such as additional herbicides.
Specifically with regard to herbicide compounds containing N- (ρhosphonomethyl)glycine, this compound is understood to be available in a variety of chemically different forms including glyphosate acid and glyphosate salts. These glyphosate compounds are described as being useful in herbicide compositions in their salt form, or as glyphosate acid, in combination with specific surfactants as a water-soluble free-flowing solid formulation. See, for example, United States patent numbers 5,118,338, 5,668,085, and 5,994,271. The salts of glyphosate, e.g., ammonium, sodium, isopropylammonium, and trimesium, are considered to be very soluble in water, while the acid form is not.
New forms of effective herbicide compositions are always desirable, especially those that can show advantages in processing, application, environmental profile (e.g., volatility), or efficacy.
Summary of the Invention
The invention relates to suspension concentrates that include the herbicide compound glyphosate acid, in the acid form, and derivatives and uses of those suspension concentrates. The suspension concentrates can be used in their suspension concentrate form to control plant growth, or can be used to prepare derivative herbicide compositions for application to control plant growth. For example, the suspension concentrate can be combined with an acidifying agent,, e.g., in a tank mix procedure or otherwise, to form a herbicide application composition, and can optionally be further combined with other ingredients such as an additional, different active herbicide compound. Preferred herbicide application compositions can have a pH below about 2.6 or 2.3, or otherwise below the pKa of glyphosate acid compound.
The suspension concentrate has been found to be easily and efficiently producible with the use of one or more other ingredients such as surfactants (wetting agents), dispersants, thickeners, etc., one or more of which optionally in combination with one or more of mixing, agitation, and milling, etc., can allow glyphosate acid particles to be suspended and/or dispersed in water to form a suspension concentrate.
The use of a herbicide composition containing glyphosate in the acid form provides efficiency because the acid form does not need to be converted to the glyphosate salt form during processing or prior to application, as is often done with the glyphosate herbicide compound (because the salt forms are more soluble in water). Instead, the suspension concentrate of the invention, including the glyphosate acid herbicide in its glyphosate acid form, is simple and economical to produce, and can be efficiently distributed, prepared, and applied without taking steps to convert the glyphosate herbicide out of its acid form. The invention can also advantageously provide improved efficacy of the glyphosate acid herbicide compound, especially when used in combination with acidifying agents. The glyphosate acid suspension concentrates have other benefits when compared to other herbicide formulations such as the absence of dust; reduction of toxicity or flammability, etc.; they do not require organic solvents; they can exhibit increased efficacy, for example due to lower particle size; they benefit from a low packing volume as compared to other forms of herbicides such as powers; and the suspension concentrates are relatively easy to handle.
In addition, the acid form of glyphosate acid, due to its uncharged state, can be advantageously less affected or unaffected by hard water, e.g., less susceptible to de-activation by hard water. An aspect of the invention relates to a suspension concentrate comprising glyphosate acid particles suspended in water and surfactant selected from the group consisting of cationic surfactant, anionic surfactant, and mixtures thereof.
Another aspect of the invention relates to suspension concentrates comprising glyphosate acid and short chain alcohol ethoxylate nonionic surfactant, e.g., having a short chain branched or linear alkyl having from 3 to 23 or fewer carbon atoms.
Yet another aspect of the invention relates to a herbicide composition comprising a suspension concentrate comprising glyphosate acid, and acidifying agent other than sulfuric acid in an amount so the pH of the herbicide composition is below the pKa of glyphosate acid.
Another aspect of the invention relates to a herbicide composition comprising a suspension concentrate comprising glyphosate acid. The herbicide composition also includes acidifying agent other than sulfuric acid, in an amount so the pH of the herbicide composition is below the pKa of glyphosate acid.
Another aspect of the invention relates to a method of applying a herbicide composition, the method comprising: preparing a herbicide composition comprising a suspension concentrate comprising glyphosate acid, and acidifying agent other than sulfuric acid, the acidifying agent being included in an amount so that the pH of the herbicide composition is below the pKa of glyphosate acid; and applying the herbicide composition to control plant growth.
Still another aspect of the invention relates to a method of preparing a suspension concentrate comprising glyphosate acid. The method comprises: combining glyphosate acid particles with water and surfactant selected from anionic surfactant, cationic surfactant, short chain alcohol ethoxylate nonionic surfactant, and mixtures thereof; and mixing or agitating the water, glyphosate acid particles, and surfactant to produce a suspension concentrate.
Still a further aspect of the invention relates to a method of preparing a suspension concentrate comprising glyphosate acid. The method comprises: combining glyphosate acid particles with water, surfactant, and dispersant; wet milling the mixture of glyphosate acid particles, water, surfactant, and dispersant, to reduce the size of glyphosate acid particles to a size that can be suspended in the water, surfactant, and dispersant; and using a high speed mixer to mix the water, glyphosate acid particles, surfactant, and dispersant, to produce a suspension concentrate comprising the glyphosate acid particles.
Yet another aspect of the invention relates to a method of preparing a herbicide composition comprising glyphosate acid. The method comprises preparing a suspension concentrate composition by a method comprising: combining glyphosate acid particles with water and one or more of surfactant and dispersant; mixing or agitating the water, glyphosate acid particles, and one or more of surfactant and dispersant, to produce a suspension concentrate containing the glyphosate acid particles; and combining the suspension concentrate composition with acidifying agent other than sulfuric acid.
Detailed Description
Glyphosate (N-(phosphonomethyl)glycine) compounds (or "glyphosate"), and chemical derivatives thereof, are a known type of active herbicide compound. Glyphosate is generally considered a broad spectrum, post-emergent, systemic herbicide effective for the control of many annual and perennial grasses and broadleaf weeds, in addition to many tree and wooden brush species both in cropland and noncrop sites. Glyphosate is available in the acid form, referred to as glyphosate acid, and is also available and more commonly used for herbicide application in it's various salt forms, such as its isopropylamine (IPA) salt form. These salt forms are considered to be generally soluble in water, which encourages the use of the glyphosate salt forms. Glyphosate is sold as the isopropylamine salt under the trade name Roundup®. The invention relates to herbicide compositions that include glyphosate acid, i.e., glyphosate (N-(phosphonomethyl)glycine), in the acid form. The term "herbicide composition" refers to compositions that include a herbicide compound, specifically here, glyphosate acid. Herbicide compositions include the described suspension concentrates and derivatives thereof. Glyphosate acid is generally considered to be an insoluble active herbicide compound. This means, for example, depending on temperature and pH, that glyphosate acid can be soluble in water or acidic water only up to a few weight percent, meaning that approximately 100 grams of an aqueous solution can dissolve only approximately a couple of grams of glyphosate acid, e.g., approximately 1 gram, or one weight percent. The glyphosate compound (N- (phosphonomethyl)glycine) includes 4 acidic protons which are removed at pKat of 0.8 (1st phosphonic), pKa2 2.3 or 2.6 (carboxylate), pKa3 6.0 (2nd phosphonic), and pKa 11.0 (amine). For purposes of the present description, when discussing the pKa of the glyphosate acid form of the N-(phosphonomethyl)glycine, the pKa2 is specifically meant, because this is the pKa that relates to the conversion of the glyphosate compound to and from the protonated and deprotonated carboxylic acid form, which is generally considered to be the "acid" form of the glyphosate herbicide compound. See, for example, http://www.soils.wisc.edu/virtual_museum/glyphosate/glyphosate_tx.html, which is part of the Virtual Museum of Minerals and Molecules, originally released 25 Dec, 1999, and last modified 31, Dec, 2000. Glyphosate acid is commercially available, generally in the form of a granular, solid, powder form or as a wet cake, for example from Dow Chemical Co., under the tradename Glyphosate WC. These materials are sold in the form of solid glyphosate acid particles having an average size (diameter) in the range from about 5 to about 18 microns. According to the invention, glyphosate acid is incorporated into a suspension concentrate. The term "suspension concentrate" as used herein, means a composition also sometimes referred to as an "aqueous flowable" or a "water- based flowable" composition, which compositions are known in the herbicide art and include or consist of particles of a generally insoluble solid active herbicide compound in suspension (preferably concentrated suspension) in water.
The suspension concentrates described herein can be produced with particles of glyphosate acid by suspending and preferably dispersing the particles in water with the assistance of other ingredients such as conventional dispersants, surfactants (wetting agents), and other optional ingredients. The glyphosate acid should be in the form of particles that exhibit physical characteristics such as size, shape, surface features, etc., that will allow the glyphosate acid particles to be suspended in water as described. The particle size range can vary depending on factors such as the other ingredients used to prepare the suspension concentrate and their respective amounts, but exemplary particles may be in the size range below about 10 microns, for example in the range from about 4 or 5 to about 7 or 8 microns. The suspension concentrate includes water in a useful amount, such as an amount that, in combination with one or more other ingredients described herein (e.g., such as surfactant and/or dispersant) will allow suspension and preferably dispersion of the glyphosate acid particles. Relative amounts of water and the other ingredients used to prepare a suspension concentrate can be any amounts that produce a useful herbicide composition in the form of a suspension concentrate. Relative amounts of different ingredients (water, glyphosate acid, surfactant, etc.) in any particular composition can depend on the intended application (including the plant to be controlled or the crop to be protected), the mode of application (e.g., field or aerial spraying or application from a hand-held spray applicator, or other technique), the method of any preparation from a suspension concentrate to a herbicide application composition, the amounts and identities of other ingredients added to the suspension concentrate, etc. Useful amounts of water in a suspension concentrate may be, for example, in the range from about 20 to about 60 weight percent water based on the total weight of the suspension concentrate, such as from about 30 to about 50 weight percent water in a suspension concentrate.
A wetting agent (also referred to herein as "surfactant"), can be used to facilitate suspending the glyphosate acid particles in a suspension concentrate. Surfactants can lower the surface tension of the water, helping to replace air on the surface of particles of the glyphosate acid with water, thereby suspending the particles. During milling (see below), new particle surfaces are created by mechanical breakdown of solid glyphosate particles. The surfactant adsorbs onto the particle surfaces to give rise to fluidity of the suspension.
A very large variety of surfactants are known and commercially available, including such different classes as cationic surfactants, anionic surfactants, non- ionic surfactants, ionic surfactants, and amphoteric surfactants, etc. The surfactant can be a surfactant or combination of surfactants useful to suspend particles of glyphosate acid. Examples of some preferred surfactants include cationic, certain non-ionic surfactants, and anionic surfactants, either alone or in combinations (e.g., blends of cationic and nonionic surfactants). Of these, particular types of preferred surfactants include non-ionic linear or branched alcohol ethoxylate surfactants, anionic phosphoric acid ester surfactants (sometimes referred to as "phosphate ester" surfactants), and cationic ethoxylated tallow amine surfactants. An example of useful surfactant would include nonionic wetting agents such as Surfonic LI 2-6, from Huntsman. Other examples of commercially available surfactants of these general classes include the following:
TRADE NAME COMMON NAME FUNCTION GENERAL
CLASSIFICATION
Tomadol 1-5 11 carbon 5 mole linear alcohol wetting agent nonionic
Surfonic L12-6 12 carbon 6 mole linear alcohol wetting agent nonionic
Trymeen 6607 20 mole tallow amine wetting agent/adjuvant cationic
Stepfac 8170 phosphate ester dispersant/adjuvant anionic
Surfonic PE 1218 phosphate ester dispersant/adjuvant anionic
Surfonic OP-70 7 mole octylphenol wetting agent/adjuvant nonionic
Tergitol NP-9 9 mole nonylphenol wetting agent/adjuvant nonionic
Soprophor 796P tristerol phenol EO/PO dispersant nonionic
Soprophor FLK tristerolphenol potassium phosphate dispersant anionic
Polyfon H sodium lignosulfonate dispersant anionic
Morwet D425 napthalene formaldehyde condensant dispersant anionic
Morwet IP naphthalene sulfonates wetting agent anionic
Pluronic L1061 block copolymer disperant nonionic
Tersperse 4984 block copolymer/alcohol ethoxylate dispersant, wetting nonionic
Tersperse 2500 surfactant dispersant anionic
Surfonic DOS60 sulfosuccinate wetting agent anionic
LI-700 lecithin derivative adjuvant nonionic
Goodrite K732 polyacrylic acid dispersant anionic
An anionic surfactant is a surface-active molecule in which an active portion of a lipophilic portion of the molecule forms a negative ion (i.e., anion) when placed in aqueous solution. Exemplary anionic surfactants include phosphoric acid ester surfactants (sometimes referred to as "phosphate ester" surfactants), sodium alkyl naphthalene sulfonate surfactants, and ethoxylated tristyrylphenol phosphate salts.
Exemplary sodium alkyl naphthalene sulfonate surfactants include sodium butyl naphthalene sulfonate, sodium di-n-butyl naphthalene sulfonate, sodium diisopropyl naphthalene sulfonate, sodium dimethyl naphthalene sulfonate, and mixtures thereof. Sodium butyl naphthalene sulfonate is commercially available, for example, under the trade name "MORWET B" from Witco/Crompton, Greenwich, CT. Sodium di-n-butyl naphthalene sulfonate is commercially available, for example, under the trade name "MORWET DB" from Witco/Crompton, Greenwich, CT. Sodium diisopropyl naphthalene sulfonate is commercially available, for example, under the trade name "MORWET IP" from Witco/Crompton, Greenwich, CT. Sodium dimethyl naphthalene sulfonate surfactant is commercially available, for example, under the trade name "SELLOGEN HR" from Henkle Corp., Cincinnati, OH.
An exemplary ethoxylated tristyrylphenol phosphate potassium salt surfactant is commercially available, for example, under the trade name "SOPROPHOR FLK" from Rhodia, Cranbury, NJ. A nonionic surfactant is a surface-active molecule that does not contain ionizable polar end groups but does contain hydrophilic and lipophilic portions. Exemplary nonionic surfactants include polyoxyethylene alkylether or alkenylether surfactants. Nonionic surfactant used to prepare a suspension concentrate as described herein may include long or short chain alcohol ethoxylate surfactant. The alcohol ethoxylate surfactant may be branched or linear.
An example of a useful nonionic polyoxyalkylene surfactant includes alcohol ethoxylate having the general formula:
R-O-((CH2)xO)y-H
wherein R may be "long" or "short" chain and "branched" or "linear" alkyl. R preferably can be a "short chain" branched or linear alcohol, meaning that it can have from about 3 to 23 or fewer carbon atoms. With respect to the oxyalkylene, x can preferably be in the range from about 2 to 5, preferably from about 2 to 4 (e.g., 2 or 3, for a polyoxyethylene or polyoxypropylene, respectively) and y can preferably be in the in the range from 5 to 25.
Examples of useful short chain nonionic polyoxyalkylenes include linear alcohol polyoxyethylenes having the general formula:
CH3(C2H4)mO(C2H4O)nH wherein CH3(C2H4)mis a short chain linear alkyl having from about 3 to 23 or fewer carbon atoms (i.e., m can be in the range from about 1 to 11 carbon atoms), and n is in the range from about 5 to 25.
Another example is short chain nonionic polyoxypropylenes having the general formula:
CH3(C2H4)mO(C3H6O)nH,
wherein CH3(C2H4)mis a short chain linear alkyl having from about 3 to 23 or fewer carbon atoms (i.e., m can be in the range from about 1 to 11 carbon atoms), and n can preferably be in the range from about 5 to 25.
Exemplary short chain linear alcohol ethoxylate surfactant are commercially available, for example, under the trade names "SURFONIC LI 2-6" from Huntsman, Austin, TX, "SURFONIC L24-7" from Huntsman, Austin, Texas, "TERGITOL 15-S-7", "TERGITOL 24-L-60", "ALPHONIC 1012-60",
"ALPOHONIC 1414-60", "BIOSOFT ET 630," from Stepan Company, Chicago, IL, and "GENOPAL 24-L-60."
Other exemplary surfactants include polyethylene glycol, fatty acid ethoxylates, phosphate esters, octyl phenol ethoxylates, and nonyl phenol ethoxylates.
Useful polyethylene glycol surfactants are commercially available, for example, under the trade names "ADEKA PEG" from Asahi Denka Kogyo, Tokyo, Japan.
Useful fatty acid ethoxylate surfactants are commercially available, for example, under the trade names "NINEX MT-610", "NINEX MT-615", and "NINEX MT-630" from Stepan, Northfield, IL.
Useful phosphate ester surfactants are commercially available, for example, under the trade names "STEPFAC 8180", "STEPFAC 8181", and "STEPFAC 8182" from Stepan. Useful octyl phenol ethoxylate surfactants are commercially available, for example, under the trade name "MAKON OP-9" from Stepan, Northfield, IL. Useful nonyl phenol ethoxylate surfactants are commercially available, for example, under the trade names "MAKON 4", "MAKON 6", "MAKON 8", "MAKON 10", "MAKON 12", and "MAKON 14" from Stepan, Northfield, IL.
A cationic surfactant is a surface-active molecule in which an active portion of a lipophilic portion of the molecule forms a positive ion (i.e., cation) when placed in aqueous solution. In one embodiment, exemplary cationic surfactant includes ethoxylated tallow amine.
The amount of surfactant ("surfactant" refers to one or a combination of surfactants) can be any amount that will allow the preparation of a suspension concentrate. Useful amounts of surfactant will be apparent to the skilled artisan based on this overall description, with exemplary amounts being below about 20 percent by weight surfactant based on the total weight of suspension concentrate, such as in the range from about 0.1 or 1 to about 10 or 15 weight percent surfactant based on the total weight of the suspension concentrate with a particularly preferred range being from 0.5 to 3 weight percent.
A dispersant can also be useful to facilitate preparation of a suspension concentrate containing glyphosate acid particles. A dispersant can stabilize and maintain a separation between the suspended particles, which otherwise may have a tendency to flocculate due to attractive forces. Dispersants can provide repulsive forces to balance the tendency to flocculate. An example of a useful type of dispersant is a nonionic dispersant such as Tersperse 4892 from Huntsman. Other examples of dispersants are listed in the table above.
The amount of dispersant can be any amount that will allow the preparation of a suspension concentrate, and that may help to stabilize a suspension concentrate, e.g., by preventing flocculation. Useful amounts may depend on the type of dispersant and the composition of the suspension concentrate, as will be apparent to the skilled artisan. Exemplary amounts of dispersant can be below about 10 or 8 percent by weight dispersant based on the total weight of the suspension concentrate, with preferred amounts being from about 2 to about 6 weight percent dispersant based on the total weight of the suspension concentrate. Other ingredients, additives, or adjuvants can also be included in the suspension concentrate, as will be appreciated by those skilled in the relevant arts. For example, an antifreeze may be useful, such as propylene glycol or other low molecular weight alcohols or polyols, in an amount to reduce the freezing point of the suspension concentrate. The amount of the antifreeze can be any amount that is useful, as will be understood by the skilled artisan. Exemplary amounts of antifreeze can be below about 20 weight percent based on the total weight of the suspension concentrate, for example from 1 to about 15 weight percent, or from about 5 to about 10 weight percent.
Thickeners can be included in the suspension concentrate to provide gravitational stabilization by increasing viscosity. Useful thickeners include chemical compounds and polymeric materials that will be known to and understood by the skilled artisan, and include, generally, natural and synthetic starches, gums, and other types of chemical compounds that will increase the viscosity of a solution. Thickening agents are well known in the chemical and polymer arts, and include, inter alia, polyacrylamides, cellulosic resins and functionalized cellulosic resins, polyacrylic acids, polyethylene oxides, and the like. Commercially available examples include Kelzan and Rhodaopl 23 xanthan gums, Attagel 50 and Attaflow FL clays, Carbopol 910 polyacrylic acid polymer, Kelcosol sodium alginate, and Bentolite purified Bentonite.
A useful amount of thickener will result in increased viscosity and stability, without causing viscosity build that would be excessive for application of the composition as a herbicide. Amounts below about 5 or 10 weight percent, based on the total weight of the suspension concentrate, may generally be useful. Preferred amounts may be less 0.5 weight percent for gums or cellulose resins. Another ingredient in a suspension concentrate can be an antifoaming agent. Antifoaming agents are well understood in the chemical and herbicide arts, and a variety of useful examples are commercially available. Antifoam agents are substances such as silicones, organic phosphates, and alcohols, which inhibit the formation of bubbles in a liquid by reducing surface tension. One specific example of a commercially available antifoam agent is SAG 10 (a 10% silicone in water), from Witco OSI. The amount of antifoaming agent used in a suspension concentrate will also be apparent to the skilled artisan, with typical amounts being less than 1 percent by weight, e.g., less than 0.5 percent by weight. Other useful additives or adjuvants to the suspension concentrate may include other surfactants, antimicrobial agents, anticorrosion agents, and other ingredients that; will be understood to be useful, in amounts that will also be understood. Surfactants having functions of wetting, spreading, or penetrating, preferably to improve efficacy of a herbicide composition, may also be added to the formulation or can be added when a tank mix is made for application. Organic solvents may be included in the suspension concentrate if desired, but are generally not used or needed.
The ingredients can be combined by known methods, including mixing, agitating, and dispersing, and, if needed or otherwise desired, milling of the glyphosate acid particles, to produce a suspension concentrate. Any of the mixing, milling, agitating, dispersing, or combining steps can be done in any order, such as milling the glyphosate acid particles and adding the milled particles to water and other ingredients, or by adding the particles to water and other ingredients followed by wet milling.
One exemplary method of producing a suspension concentrate starts with glyphosate acid particles in the form of a wet cake or dry (granular, powder) acid, generally having a relatively large particle size (e.g., greater than about 10 microns). The wet cake or dry particles of that size can be mixed or dispersed into a liquid. This can be done, for example, by combining the glyphosate acid particles with water and other ingredients with agitation or mixing to disperse the particles. For example, the glyphosate acid particles can be added to water and one or more of surfactant, dispersant, antifreeze, and antifoam, and mixed using a highspeed mixer to disperse the glyphosate acid particles. The mixture of glyphosate acid, water, and other ingredients can be further processed toward a suspension concentrate by methods that will process the glyphosate acid particles into a form that allows suspension of the particles in water in the form of a suspension concentrate, for instance by reducing the size of the particles in the presence of a useful surfactant. Thus, a processing step can be to reduce the size of glyphosate acid particles to a size that will allow the particles, in combination with one or more of the other ingredients described herein such as surfactant and/or dispersant, to be maintained in a stable suspension concentrate composition. An exemplary method of reducing the size of the glyphosate acid particles is by using milling techniques, e.g., what is referred to as "wet milling." A typical such average particle size can be below about 10 microns, for example in the range from about 4 to about 8 microns or from about 5 to about 7 microns. Any method of reducing particle size may be useful, such as by using an attrition mill, ball mill, sand mill, or other milling process.
After reduction of the particle size, the solution containing the suspended glyphosate acid particles can be further combined with a thickener, by mixing the thickener into the solution. The suspension concentrate can preferably be stable in the form of a suspension concentrate for a useful period, meaning that the suspension concentrate composition does not settle or otherwise transform out of the suspension concentrate form, and maintains the form of a suspension concentrate, for a useful amount of time. Useful periods of stability can depend on timing, e.g., between preparation, further processing of, and use (application) of the suspension concentrate, which time periods may vary greatly based on convenience, preference, inherent stability of the suspension, or other factors. If a suspension concentrate or a derivative form of the suspension concentrate can be applied in a short or very short period of time after preparation, longer-term stability is not required. Exemplary suspension concentrates of the invention have been found to be stable at approximately room temperature and in substantially undisturbed and un-agitated environments for periods in excess of 6 or 12 months. Longer or shorter periods would also be useful.
The suspension concentrate can be applied directly to a field or plant to control undesired plant growth, or can be combined with other ingredients to form a derivative herbicide composition for application which can be applied to a field or plant, e.g., as a "herbicide application composition" to control undesired plant growth. "Herbicide application composition" refers to a herbicide composition having a concentration of herbicide compound (here, glyphosate acid) that would normally be applied to a field or plant to control undesired plant growth, as opposed, for example, to compositions having higher concentrations of herbicide compound that sometimes occur in preparation, storage, shipping, or sale of a herbicide composition. It is noted that suspension concentrate compositions as described herein are capable of controlling plant growth if applied directly to a plant. Yet it can be typical for reasons of efficiency, cost, convenience, techniques presently used in applying herbicide compositions, and environmental considerations, to use a relatively diluted form of herbicide compositions to conveniently apply a specific and known amount of herbicide compound per acre or per other unit of application. By way of example, herbicide application compositions include any herbicide composition having such a specific concentration of glyphosate acid for application, e.g., to a field, and specifically include suspension concentrates and derivatives prepared by combining the suspension concentrate with one or more of water, acidifying agent, another herbicide, or other ingredients, as will be described in more detail below.
Additional ingredients can be added to the suspension concentrate to produce a derivative herbicide composition or herbicide application composition. These added ingredients may be useful in the herbicide composition for purposes of dilution, stability, pH adjustment, anti-foaming, or to otherwise facilitate application or increase efficacy. These other ingredients may be added to the suspension concentrate or derivative herbicide composition at any time and in any order, as desired or convenient. Exemplary additional ingredients include water, antifoaming agents, acidifying agents, anticorrosion agents, or additional active herbicide compounds, such as described, for example, in Applicants' copending U.S. Patent Application entitled "Herbicide Compositions Comprising Imidazolinone Acid, Methods of Preparation, and Methods of Use," having Attorney Docket No. UAP0008/US/2, U.S. Serial No. , filed on even date herewith.
A preferred embodiment of a herbicide composition of the invention, comprising or prepared from a suspension concentrate comprising glyphosate acid, can further include acidifying agent, particularly an acidifying agent that improves the efficacy of the herbicide composition. Examples of a certain type of acidifying agent are described in United States Patent Numbers 4,445,925, 4,994,101,
5,288,692, (Young). Other exemplary acidifying agents are known, and still others are described in Assignee's copending United States Patent Application entitled "Herbicide Composition Comprising Herbicide Compound in Acid Form and Acidifying Agent," having Attorney's Docket Number UAP0006/US/2, and United
States Patent Application serial number , filed on even date herewith.
See also Assignee's copending United States Patent Application entitled "Herbicide Microemulsion-Forming-Concentrates, Microemulsions, and
Methods," having Attorney's Docket Number UAP0003/US/2, and United States
Patent Application serial number , filed on even date herewith. A preferred herbicide application composition can be formulated to include an acidifying agent, and most preferably to include sufficient acidifying agent to exhibit a pH that is below about 2.6, preferably below about 2.3, e.g., below the pKa of glyphosate acid.
While wishing not to be bound by theory, it is believed that the direct application of the acid form of glyphosate, especially as part of a herbicide composition having a pH below the pKa of the glyphosate acid compound, can effect improvements in plant control by one or both of the following mechanisms. First, a neutral (acid) molecule can have an easier time penetrating a cuticle on a plant, compared to a charged (salt) molecule. Secondly, an acidifying agent and a low pH of a herbicide composition can have a damaging effect on a plant's surface, thereby letting more herbicide penetrate the surface. Also, the neutral acid molecule can be less susceptible to de-activation by hard water.
A variety of different acidifying agents can be useful with the herbicide compositions of the invention. The particular acidifying agent chosen and the amount used can be based on factors including the intended use or application of the herbicide composition (including the identity of the target undesirable plant growth and any nearby desirable plant growth) the method of application, physical and chemical properties of the herbicide application composition, and others. The acidifying agent may be any of a variety of suitable organic or inorganic acids, of any useful strength or concentration, that can be added to a suspension concentrate or a derivative thereof, preferably without causing substantial or undue negative effects such as reaction with an ingredient of the suspension concentrate such as the glyphosate acid, precipitation, etc. It will be understood that an acidifying agent can be in a concentrated or diluted form, as necessary or desirable. Non-limiting examples of acidifying agents include acids such as sulfuric acid, phosphoric acid, hydrochloric acid, nitric acid, acetic acid (e.g., "glacial" acidic acid), perchloric acid, polyphosphoric acid, acidic adducts such as the sulfuric acid adducts described in United States Patent Number 5,288,692 (Young), especially the adduct of sulfuric acid and urea, or any other acidifying agent that can be used to affect the pH of a herbicide composition, especially to prepare a herbicide composition including glyphosate acid and having a pH below the pKa of glyphosate acid. These and other acidifying agents can be used alone or in combination. Just one specific example of a useful type of acidifying agent includes adducts of sulfuric acid, and an "amide" according to the formula:
Figure imgf000018_0001
wherein X is chalcogen, and each of Ri, R2 and R3 is independently selected from hydrogen and organic radicals. As used herein, "amide" encompasses all compounds of formula (1 ) regardless of the chalcogen. The molar ratio of amide to acid is usually in the range of about 1/4 to less than 2 so that at least some of the acid is present as the monoamide-acid adduct.
When Ri, R2, and R3 are organic radicals, they may be cyclic or acyclic, straight or branched chained, and can contain one or more heteroatoms such as sulfur, nitrogen, oxygen, phosphorus and the like. Further, Ri, R2 and R3 can contain one or more substituents such as thiol, hydroxy, nitro, amino, nitrile, amide, ester and halogen groups and others. Such organic radicals may contain aryl groups such as aralkyl and alkaryl groups. Certain preferred organic radicals can be free of olefinic or alkynyl unsaturation and can generally have up to about 20, preferably up to about 10 carbon atoms. Particularly preferred amides include urea, thiourea, formamide, dimethylformamide, biuret, triuret, thioformamide, and combinations of these.
The chalcogens are elements of Periodic Group VI-B and include. oxygen, sulfur, selenium, tellurium, and polonium. Oxygen and sulfur can be preferred due to low cost, availability, low toxicity, and chemical activity, and oxygen is the most preferred.
A specific example of an adduct according to formula (1) can be the sulfuric acid/urea adduct:
N H 2
I
H N Q
H
(2) O
O O H
Other types of useful acidifying agents include various forms of sulfuric acid, phosphoric acid, hydrochloric acid, nitric acid, acetic acid (e.g., "glacial" acidic acid), perchloric acid, polyphosphoric acid, adducts of these, etc. Various such acids are commercially available in different forms and concentrations, such as solids, liquid (aqueous) solutions, concentrated liquid solutions, etc., or can be prepared by one of skill. Any such form of acidifying acid may be useful to reduce the pH of a herbicide composition prepared from or comprising the suspension concentrate, preferably without causing any undue negative affects. The chosen form of acidifying agent may be based on commercial availability, convenience, and the overall desired properties of the herbicide composition, its different ingredients (e.g., the herbicide compound), and its desired method of preparation and use. The amount of acidifying agent added to a suspension concentrate or herbicide application composition can be based on factors including the particular composition and chemistry of the suspension concentrate or herbicide application composition, including the amounts and chemistries of surfactant and herbicide compound; the amount of water; the type of acidifying agent and its chemistry and strength (concentration); the desired pH; etc. Preferred amounts of any particular acidifying agent can be capable of improving the efficacy of the herbicide composition as applied, and particularly preferred amounts will be sufficient to produce an application composition having a pH below 2.3 or 2.6, or otherwise below the pKa of glyphosate acid compound.
Examples of useful amounts of acidifying agent will be quite varied considering the above factors. Relatively strong concentrations of liquid (aqueous) acidifying agent solutions such as 93% liquid sulfuric acid, 72% phosphoric acid, 85% polyphosphoric acid, 90% nitric acid, 99% glacial acetic acid, etc., can be added directly or can be first diluted and then added to a suspension concentrate or a derivative formulation in an amount to bring the pH below about 3, e.g., below about 2.6 or 2.3, or lower. In terms of volume percent, very generally speaking, useful amounts of aqueous acidifying agent such as those listed above can be below about 5 or 10 volume percent, e.g., in the range from about 0.01 to about 4 parts by volume aqueous acidifying agent based on the total by volume of suspension concentrate and acidifying agent. Volumes of acidifying agent outside of this range may also be useful, depending on the composition and strength of the acidifying agent and the desired pH.
The herbicide compositions can be used for immediate and long-term, post- emergent control of a large variety of different forms of vegetation. As an example, the suspension concentrate could be applied directly to plants for controlling plant growth, although this may include an unnecessarily potent concentration of the glyphosate acid. Furthermore, it may as a general matter be difficult to uniformly apply a small amount of concentrated herbicide composition to a large area without dilution. A suspension concentrate would instead more likely be a product sold commercially as a herbicide concentrate product, which would be a composition that includes a relatively high concentration of glyphosate acid active herbicide compound, as manufactured or packaged for sale, and which may typically be diluted or combined with other ingredients prior to use to form a herbicide application composition.
The suspension concentrate could be purchased by distributors or suppliers, or directly by consumers such as farmers, any of which could add optional ingredients such as water, an acidifying agent (e.g., in the form of a solid, powder, or an aqueous solution, etc.), or another type of herbicide formulation or herbicide compound, to the suspension concentrate. The additional ingredients could, for example, be added and mixed in a tank immediately prior to application. The suspension concentrate would typically be diluted with water. A typical dilution would be 1 pint of suspension concentrate in 15 gallons of water for ground application. Another typical dilution would be 1 pint of suspension concentrate in 3-5 gallons of water for application by air.
In one embodiment of a distribution system, a suspension concentrate could be sold to farming product or nursery dealers, or the like, who could dilute the suspension concentrate with water and/or add other ingredients such as an acidifying agent or other herbicide. This could be particularly convenient if such a dealer normally kept a stock of acidifying agent such as phosphoric acid or sulfuric acid, etc. The suspension concentrate combined with acidifying agent by the dealer could be sold to an end consumer who could use the composition as purchased or who could optionally further dilute the purchased composition or add other ingredients to the purchased composition such as an additional herbicide by tank mixing.
Alternatively, the suspension concentrate could be sold directly to end users who could add one or more of the additional ingredients in a tank mixing process. For example, the suspension concentrate could be combined with water or an acidifying agent or both, in a tank, by a farmer, and then applied. The herbicide compositions can be applied for immediate vegetation control by contact killing, by application of a herbicide application composition to plants. As will be understood by the skilled artisan, herbicide application compositions as described can contain a useful amount of the glyphosate acid active herbicide compound, based on factors of efficacy, safety, application rate, etc. Similarly, a useful amount of herbicide application composition (containing the useful amount of glyphosate acid) to be applied to a plant or a field, will be readily understood by those of skill, based, e.g., on desired efficacy, safety, application rate, and environmental factors, etc.
The particular amount of glyphosate acid in any specific herbicide application composition will depend on factors known and as described above. Advantageously, it has been found that certain preferred herbicide application compositions of the invention, especially those that include an acidifying agent, and in particular those that also have a reduced pH, e.g., below about 3, 2.6, or 2.3, can be applied at lower dosages or "application rates" (lower amounts of herbicide compound per plant or per acre) relative to other herbicide compositions containing other forms of glyphosate (e.g., the salt form), or not at a reduced pH as described.
Examples of dosages ("application rates") of glyphosate acid, especially as included in a herbicide compositions of the described pH, to a field, can be in the range from about 1/100 to about 6 pounds glyphosate acid per acre, with dosages in the range from about 0.03 to 0.5 pounds per acre being particularly preferred. More resistant plants or different field environments may require higher concentrations and/or higher dosage rates. The preparation of herbicide application compositions suitable to apply useful dosages, based on the concentration of herbicide compound in a suspension concentrate, will be understood by one of ordinary skill. The herbicide compositions can, as indicated, be applied using conventional aerial or ground spray techniques in field applications. The herbicide compositions can also be applied by any other useful technique, such as by spot- application to undesired plant growth using a hand-held applicator, or the like.
Advantageously, herbicide compositions of the invention have been found to exhibit the additional advantages of being relatively non- volatile. The advantage of non- volatile herbicide compositions are self-evident to those of skill in the herbicide arts. A non- volatile herbicide composition has the advantage of not evolving, or evolving to a reduced degree, through the air, to inadvertently contact desired plant growth. In practical effect, this advantageous property allows the herbicide compositions of the invention to be applied to undesired plant growth in greater strength or in closer proximity to desired above-ground plant growth.
Vegetation that can be controlled using the herbicide compositions of the invention include any type of vegetation that is or is known to be controlled by glyphosate or glyphosate acid herbicide compounds. The ingredients of the herbicide compositions, e.g., surfactant, dispersant, acidifying agent, etc., can be selected in view of the type of control desired (i.e. pre-emergent or post-emergent) and the type of vegetation to be controlled according to the known attributes of glyphosate compounds, including glyphosate acid.
EXAMPLES A typical suspension concentrate containing 3 lb glyphosate acid per gallon can be prepared as described herein, from ingredients including:
Water 41.60%
SAG 30 Antifoam 0.30
Propylene Glycol 5.00
Surfonic T-l 5 8.00 tallow amine 15 mole
86% glyphosate wc 36.10 wet cake
Tersperse 4984 2.00 dispersant
2% Kelzan 0.5% Proxel 7.00
Other exemplary suspension concentrate formulations may also include a higher amount of surfactant (e.g., 8% by weight or greater) and can have a glyphosate acid concentration of 4 pounds per gallon, as follows:
Water 32.45%
SAG 30 0.30 antifoam
Propylene Glycol 8.00 antifreeze
AU-392 8.00 nonionic/tallow amine blend
Glyphosate WC,Dow 45.30 active, 39.0% glyphosate acid
Tersperse 4894 2.00 dispersant
2% Kelzan-0.5% Proxel 4.00 thickener & antimicrobial
Total 100.00
Glyphosate Acid Content of this formulation:
39.0% w/w
480 g/L
4.0 lb/gal
In the above formulation, the 8% surfactant provides wetting for the preparation of the suspension concentrate, and upon dilution in water functions as an adjuvant to improve efficacy of the herbicide formulation. As another example of ingredients of a suspension concentrate: Water 32.45%
SAG 30 0.30 antifoam
Propylene Glycol 8.00 antifreeze
LI-700 8.00 lecithin derivative
Glyphosate WC, Dow 45.30 active, 39.0% glyphosate acid
Tersperse 2500 2.00 dispersant
2% Kelzan-0.5% Proxel 4.00 thickener & antimicrobial
Total 100.00
EXAMPLES 1-5
The following examples illustrate how suspension concentrates of the invention can be used to control plant growth, optionally with an acidifying agent.
Materials and Methods :
Experiments were conducted to evaluate the efficacy of a variety of different types of herbicide formulations, including formulations from suspension concentrates, and to evaluate the effect of adding acids to the spray solution as an adjuvant (see Data Tables for Experiment 2 and Experiment 5). Each treatment in the experiment was replicated three times. An untreated control was also included in each experiment.
Experiment one was designed to identify useful acid concentrations of four acids when used with a 2,4-D acid (2,4-dichlorophenoxy acetic acid) formulation (PCC- 1133), or a glyphosate (N-(phosphonomethyl)glycine) acid formulation (PCC-1168 suspension concentrate containing glyphosate acid), in a greenhouse. These treatments were compared to standard 2,4-D and glyphosate formulations (ROUNDUP ULTRA, SABER, SALVO), and an untreated control.
Experiment two determined the effect of adding four different acid adjuvants to five formulations of glyphosate: RODEO, ROUNDUP, ROUNDUP ULTRA, ENGAME, and PCC-1168, at four different glyphosate rates. (The Kochia for experiment 2 did not germinate well.) Experiment five compared the efficacy of the glyphosate acid formulation PCC- 1168, to PCC-1168 containing a variety of acidifying agents.
PCC-1168 Suspension Concentrate Formulation
INGREDIENT %AI-Tech %/WT
Water 44.60
SAG 30, OSI, Antifoam 0.30
Proplyene Glycol, Antifreeze 8.00
Surfonic LI 2-6, Huntsman, nonionic wetting agent 0.50
Glyphosate WC, Dow, Active Ingredient 86.00 36.10
Tersperse 4894, Huntsman, nonionic dispersant wetter 3.50
Gum 2% Kelzan-0.5%Proxel Premix, thickener & antimicrobial 7.00
(Delivers 0.14%Kelzan, 0.03% Proxel.)
Add in order listed to cowles high speed mixer stopping prior to Kelzan-Proxel addition.
Grind to 5-18 microns, 4 hrs in attritor, 60%.
Let down to mix tank with scales
Add calculated amount Kelzan/Proxel Premix to milled liquid. Blend moderately for 30 min.
PCC-1133 Microemulsion Formulation
2,4-D Acid 28.0 98% 2,4-D acid technical flake
Tomadol 1-5 32.0 11 carbon 5 mole linear alcohol ethoxylate
Tomadol 1-7 32.3 tt n u a
Rhodofac RS 710 8.0 anionic, phosphate ester surfactant
SAG 10 Antifoam 0.1
The PCC-1133 microemulsion was made by adding surfactants to a mixing vessel and warming to 130F- 150F. Antifoam and acid were added and mix in until clear, with the 2,4-D acid becoming dissolved in the surfactant, producing a MFC. A microemulsion was formed from the MFC by combining 2 ml MFC with 98 ml water with agitation.
Procedure
For each experiment conducted, greenhouse flats 26 cm2 by 6 cm deep were filled with Metro Mix 200 potting soil (experiments one and two) or Metro Mix 350 (experiments three, four, and five). The soil was pre-wetted before filling the flats. Six furrows were pressed into the soil in each flat using a custom designed form. Corn, tame oats, wheat, pinto beans, cotton, and sunflower were planted in each tray. Cottonseed was soaked for three days previous to planting to improve germination. However, germination was still unacceptable and kochia was substituted in experiments two through five. One species was planted in each of the six rows in each flat. Five seeds were planted in each row of corn, bean, and cotton, and sunflower. Six seeds were planted in each row of oat and wheat. Kochia was sprinkled evenly along the row by hand. Each flat was covered with 2 cm of soil and placed in the greenhouse. Greenhouse conditions were 28/20 C day/night temperatures and 16/8 h day night periods. Light was supplemented with 400 W sodium halide lights.
The plants were allowed to germinate and grow in the greenhouse for 2 weeks and then treated. Treatments were mixed using serial dilutions. In experiment one, the percent acid was reduced in each dilution by one half. In experiments 2 through 5 each dilution reduced the herbicide rate by one half. Acid concentrations were calculated and mixed so that a treatment with one of the acids or LI- 136 would have the same amount of acid as the treatment with PCC- 1174. Therefore, a treatment designated 4% sulfuric acid would have the same amount of acid as a treatment with 4% PCC-1174.
After mixing in experiments one, four, and five, the pH of the spray solution of each treatment was measured with a, VWR Scientific model 8005 pH meter. The pH was measured to determine if the acid used or the amount of acid added was sufficient to lower the pH below the pKa of the acid herbicides used. The pKa of 2,4-D acid in the PCC-1133 was measured to be 2.87. The pKa of glyphosate acid in PCC-1168 was measured to be about 2.5 or 2.6.
At the time of treatment, crops were at the following stages: corn - 2 to 3 If, oat - 2 to 3 If, cotton - cotyledon, kochia - 7 If, bean -1st trifoliate, and sunflower - 2 to 4 If. Plants were treated using a greenhouse track sprayer equipped with an 800 IE nozzle and calibrated to deliver 140 L ha-1 at the height of the crop canopy. Each treatment was simultaneously applied to three trays of plants, one for each replicate. After treatment, the plants were left in the head house to dry and then transferred to the greenhouse. Plants in each treatment were evaluated visually for injury 1 day, 1 week, and 2 weeks after treatment.
SUMMARY OF VARIABLES OF EXPERIMENTS
Figure imgf000027_0001
Experiment 5
Treatment rates lb/A Plants Reps
PCC-1168 0.0313 dry beans 3
PCC-1168+Sulfuric (4%) 0.0625 wheat
PCC-1168+HC1 (4%) 0.125 kochia
PCC-1168+Nitric (4%) 0.025 corn
PCC-1168+Acetic (4%) 0.5 sunflower
PCC-1168+Phosphoric (4%) oats
PCC-1168+Perchloric (4%)
PCC-1168+Polyphosphoric (4%) Following are data that illustrate the efficacy of various herbicide compositions of Experiments 1, 2, and 5. The injury caused by the herbicide treatment was rated visually. Plants were observed and compared to the untreated control. All the plants of each species in each replication were given a single rating. A rating of 0 = no injury ~ the plants look the same as the untreated. A rating of 100 = dead — usually highly necrotic, brown and no chance of producing seed. SALVO® is a commercially available product of Platte Chemical Co. containing 5 lb 2,4-D acid equivalent/gallon as 2-ethyl-hexyl ester of 2,4-D
SABER® is 2,4-D formulated as a dimethylamine salt (2,4-dichlorophenoxy dimethylamine salt), i.e., is a commercially available product of Platte Chemical Company containing 3.8 lb 2,4-D acid equivalent/gallon as dimethylamine salt.
RODEO is a soluble liquid water based formulation of IPA, glyphosate, and water, commercially available from MONSANTO, and was used according to the labeling instructions.
RODEO ULTRA is a glyphosate salt herbicide composition commercially available from MONSANTO, and was used according to the labeling instructions.
ENGAME is a soluble liquid water based formulation of glyphosate acid, urea, sulfuric acid, and water, commercially available from ENTEK, and was used according to the labeling instructions.
ROUNDUP and ROUNDUP ULTRA are commercially available IPA glyphosate salt and surfactant herbicide compositions.
Acidifying Agents
HC137% Nitric 70%
Glacial Acetic 100% Perchloric 60% Polyphosphoric 100% PCC-1174
Commercially available as "AMADS," which is urea and H2S04 in water:
Chemical Name 1-amino methanamide dihydrogen tetraoxosulfate, or sulfuric acid and urea Molecular Formula NH2C(OH)NHS04H2
Figure imgf000029_0001
INGREDIENT %/wτ
Water 22.99
93% Sulfuric Acid 48.65
99% Urea 26.64
Stepfac 8170 1.71
SAG 10 Antifoam 0.01
LI-136 = blend of 50 wt. % 21-0-0 urea liquor and 50 wt percent of 72% phosphoric acid in water. The phrase "21-0-0 urea liquor" means a liquid that contains 21% by volume urea (nitrogen), 0% by volume phosphate (phosphorous), and 0% by volume potash (potassium).
Each of the acids were used as is and combined with the PCC-1133 or PCC-1168 herbicide compositions to form a solution that contains 2 percent or 4 percent by volume of the acid solution, as indicated in the data tables, and such that the pH of the herbicide composition was below the pKa of the particular herbicide compound.
The ingredients of the herbicide compositions as applied are listed in the following data tables, and were diluted with water and used at the rates indicated for herbicide ingredients and acidifying agents. .
DATA FOR EXPERIMENT 2 (TWO WEEK) tame spring dry
Rate Units corn oat wheat bean sunflower
1 RODEO .0313 LB AE/A 0.0 0.0 0.0 0.0 0.0
2 RODEO .0625 LB AE/A 0.0 0.0 0.0 5.0 5.0
3 RODEO 0.125 LB AE/A 20.0 20.0 0.0 30.0 40.0
4 RODEO 0.25 LB AE/A 30.0 10.0 40.0 60.0 100.0
5 ROUNDUP .0313 LB AE/A 0.0 0.0 0.0 0.0 0.0
6 ROUNDUP .0625 LB AE/A 20.0 5.0 0.0 33.3 40.0 ROUNDUP 0.125 LBAE/A 70.0 70.0 60.0 50.0 90.0 ROUNDUP 0.25 LBAE/A 90.0 80.0 70.0 80.0 100.0 ROUNDUP ULTRA .0313 LBAE/A 20.0 0.0 0.0 0.0 0.0 ROUNDUP ULTRA .0625 LBAEA 30.0 20.0 40.0 50.0 40.0 ROUNDUP ULTRA 0.125 LBAE/A 90.0 49.0 70.0 70.0 90.0 ROUNDUP ULTRA 0.25 LBAE/A 100.0 80.0 90.0 80.0 100.0 ENGAME .0313 LBAE/A 20.0 0.0 0.0 60.0 60.0 ENGAME .0625 LBAE/A 40.0 20.0 20.0 60.0 63.3 ENGAME 0.125 LB AE/A 50.0 40.0 30.0 60.0 90.0 ENGAME 0.25 LBAE/A 90.0 80.0 90.0 75.0 100.0 PCC-1168 .0313 LBAE/A 0.0 0.0 0.0 0.0 0.0 PCC-1168 .0625 LBAE/A 0.0 0.0 0.0 0.0 0.0 PCC-1168 0.125 LB AE/A 20.0 50.0 10.0 20.0 16.7' PCC-1168 0.25 LBAE/A 70.0 60.0 80.0 46.7 40.0 PCC-1168 .0313 LB AE/A 50.0 30.0 5.0 40.0 40.0
PCC-1174 4 %V7V PCC-1168 .0625 LBAE/A 50.0 60.0 20.0 40.0 40.0
PCC-1174 4 %V/V PCC-1168 0.125 LBAE/A 70.0 60.0 70.0 63.3 76.7
PCC-1174 4 % V/V PCC-1168 0.25 LBAE/A 90.0 80.0 80.0 80.0 100.0
PCC-1174 4 %V7V PCC-1168 .0313 LBAE/A 10.0 10.0 10.0 40.0 5.0
SULFURIC ACID 2 % V/V PCC-1168 .0625 LBAE/A 10.0 10.0 10.0 40.0 10.0
SULFURIC ACID 2 % V/V PCC-1168 0.125 LBAE/A 50.0 20.0 10.0 60.0 28.0
SULFURIC ACID 2 %V/V PCC-1168 0.25 LBAE/A 90.0 70.0 80.0 80.0 90.0
SULFURIC ACID 2 %V/V PCC-1168 .0313 LBAE/A 0.0 0.0 0.0 0.0 1.7
PHOSPHORIC ACID 4 %V/V PCC-1168 .0625 LB AE/A 0.0 0.0 0.0 20.0 5.0
PHOSPHORIC ACID 4 % V/V PCC-1168 0.125 LBAE/A 5.0 5.0 5.0 40.0 40.0
PHOSPHORIC ACID 4 %V/V PCC-1168 0.25 LBAE/A 60.0 60.0 40.0 60.0 80.0
PHOSPHORIC ACID 4 %V/V PCC-1168 .0313 LBAE/A 5.0 0.0 0.0 10.0 20.0
LI- 136 4 %V/V PCC-1168 .0625 LBAE/A 5.0 0.0 0.0 20.0 40.0
LI-136 4 %V/V PCC-1168 0.125 LBAE/A 20.0 0.0 10.0 40.0 70.0
LI-136 4 %V/V PCC-1168 0.25 LBAE/A 50.0 50.0 60.0 70.0 100.0
LI-136 4 %VV UNTREATED 0.0 0.0 0.0 0.0 0.0 DATA FOR EXPERIMENT 5 (TWO WEEIQ tame spring dry
Rate Unit corn oat cochia wheat bean sunflower PCC-1168 .0313 LB AE/A 0.0 0.0 0.0 0.0 5.0 0.0 PCC-1168 .0625 LB AE/A 0.0 0.0 0.0 10.0 30.0 20.0 PCC-1168 0.125 LB AE/A 20.0 20.0 0.0 40.0 50.0 60.0 PCC-1168 0.25 LB AE/A 60.0 60.0 20.0 70.0 70.0 95.0 PCC-1168 0.5 LB AE/A 75.0 70.0 50.0 80.0 75.0 100.0 PCC-1168 .0313 LB AE/A 0.0 0.0 0.0 10.0 50.0 60.0
SULFURIC ACID 4 % V/V PCC-1168 .0625 LB AE/A 10.0 30.0 0.0 30.0 70.0 90.0
SULFURIC ACID 4 % V/V PCC-1168 0.125 LB AE/A 65.0 60.0 10.0 65.0 80.0 95.0
SULFURIC ACID 4 % V/V PCC-1168 ; 0.25 LB AE/A 80.0 75.0 50.0 85.0 85.0 100.0
SULFURIC ACID 4 % V/V PCC-1168 0.5 LB AE/A 100.0 100.0 95.0 100.0 98.0 100.0
SULFURIC ACID 4 % V/V PCC-1168 .0313 LB AE/A 0.0 0.0 0.0 0.0 30.0 20.0
HYDROCHLORIC ACID 4 % V/V PCC-1168 .0625 LB AE/A 0.0 0.0 0.0 10.0 50.0 65.0
HYDROCHLORIC ACID 4 % V/V PCC-1168 0.125 LB AE/A 10.0 25.0 0.0 40.0 60.0 70.0
HYDROCHLORIC ACID 4 % V/V PCC-1168 0.25 LB AE/A 75.0 70.0 10.0 60.0 80.0 90.0
HYDROCHLORIC ACID 4 % V/V PCC-1168 0.5 LB AE/A 80.0 90.0 60.0 90.0 93.0 100.0
HYDROCHLORIC ACID 4 % V/V PCC-1168 .0313 %v/v 0.0 0.0 0.0 0.0 50.0 50.0
NITRIC ACID 4 LB AE/A PCC-1168 .0625 % V/V 0.0 0.0 0.0 10.0 55.0 65.0
NITRIC ACID 4 LB AE/A PCC-1168 0.125 % V/V 15.7 25.0 10.0 40.0 60.0 75.0
NITRIC ACID 4 LB AE/A PCC-1168 0.25 % V/V 75.0 70.0 60.0 60.0 80.0 90.0
NITRIC ACID 4 LB AE/A PCC-1168 0.5 % V/V 80.0 85.0 60.0 85.0 90.0 98.0
NITRIC ACID 4 LB AE/A PCC-1168 .0313 % V/V 0.0 0.0 0.0 0.0 0.0 0.0
GLACIAL ACETIC ACID 4 LB AE/A PCC-1168 .0625 % V/V 0.0 0.0 0.0 0.0 0.0 5.0
GLACIAL ACETIC ACID 4 > LB AE/A PCC-1168 0.125 % V/V 10.0 20.0 0.0 36.7 30.0 40.0
GLACIAL ACETIC ACID 4 LB AE/A PCC-1168 0.25 % V/V 60.0 60.0 0.0 70.0 50.0 60.0
GLACIAL ACETIC ACID 4 LB AE/A PCC-1168 0.5 %v/v 75.0 75.0 20.0 80.0 70.0 95.0
GLACIAL ACETIC ACID 4 %v/v PCC-1168 .0313 LBAE/A 5.0 0.0 0.0 0.0 30.0 40.0
PHOSPHORIC ACID 4 %VV PCC-1168 .0625 LBAE/A 15.0 0.0 5.0 0.0 40.0 65.0
PHOSPHORIC ACID 4 %VV PCC-1168 0.125 LBAE/A 60.7 60.0 10.0 65.0 50.0 60.0
PHOSPHORIC ACID 4 % V/V PCC-1168 0.25 LBAE/A 80.0 75.0 20.0 85.0 70.0 95.0
PHOSPHORIC ACID 4 %V/V PCC-1168 0.5 LBAE/A 93.0 95.0 80.0 95.0 98.0 100.0
PHOSPHORIC ACID 4 %V/V PCC-1168 .0313 LBAE/A 0.0 0.0 0.0 0.0 40.0 40.0
PERCHLORIC ACID 4 % V/V PCC-1168 .0625 LB AE/A 20.0 20.0 0.0 20.0 50.0 60.0
PERCHLORIC ACID 4 %V/V PCC-1168 0.125 LBAE/A 65.0 60.0 20.0 60.0 55.0 60.0
PERCHLORIC ACID 4 % V/V PCC-1168 0.25 LBAE/A 80.0 75.0 30.0 75.0 60.0 95.0
PERCHLORIC ACID 4 %V/V PCC-1168 0.5 LBAE/A 90.0 90.0 30.0 90.0 80.0 98.0
PERCHLORIC ACID 4 %V/V PCC-1168 .0313 LBAE/A 70.0 70.0 0.0 60.0 50.0 50.0
POLYPHOSPHORIC ACID 4 %V/V PCC-1168 .0625 LBAE/A 75.0 75.0 0.0 75.0 55.0 65.0
POLYPHOSPHORIC ACID 4 %V/V PCC-1168 0.125 LBAE/A 80.0 80.0 30.0 90.0 60.0 90.0
POLYPHOSPHORIC ACID 4 %V/V PCC-1168 0.25 LBAE/A 95.0 90.0 40.0 93.0 85.0 95.0
POLYPHOSPHORIC ACID 4 %V/V PCC-1168 0.5 LBAE/A 98.0 95.0 80.0 95.0 90.0 100.0
POLYPHOSPHORIC ACID 4 %VV UNTREATED 0.0 0.0 0.0 0.0 0.0 0.0

Claims

We claim:
1. A suspension concentrate comprising glyphosate acid particles suspended in water and surfactant selected from the group consisting of cationic surfactant, anionic surfactant, and mixtures thereof.
2. The suspension concentrate of claim 1 comprising glyphosate acid particles suspended in water and surfactant selected from the group consisting of an anionic phosphoric acid ester, a cationic ethoxylated tallow amine, and mixtures thereof.
3. The suspension concentrate of claim 2 comprising a dispersant to disperse glyphosate acid particles.
4. The suspension concentrate of claim 1 wherein the glyphosate acid particles have an average particle size below about 10 micron.
5. The suspension concentrate of claim 1 wherein the glyphosate acid particles have an average particle size in the range from about 4 to about 8 micron.
6. The suspension concentrate of claim 1 wherein the suspension concentrate comprises from about 25 to about 50 parts by weight glyphosate acid.
7. The suspension concentrate of claim 1 wherein the suspension concentrate comprises from about 30 to about 40 parts by weight glyphosate acid.
8. The suspension concentrate of claim 1 comprising cationic ethoxylated tallow amine surfactant.
9. The suspension concentrate of claim 1 comprising cationic ethoxylated tallow amine surfactant and dispersant.
10. The suspension concentrate of claim 1 comprising acidifying agent.
11. A suspension concentrate comprising glyphosate acid and short chain alcohol ethoxylate nonionic surfactant having a short chain branched or linear alkyl having from 3 to 23 or fewer carbon atoms.
12. The suspension concentrate of claim 11 wherein the nonionic surfactant comprises short chain linear alcohol ethoxylate surfactant.
13. The suspension concentrate of claim 11 wherein the nonionic surfactant has the formula:
CH3(C2H2)mO(C2H4O)nH
wherein m is in the range from 1 to 11 and n is in the range from about 5 to 25.
14. A herbicide composition comprising a suspension concentrate comprising glyphosate acid, and acidifying agent other than sulfuric acid, in an amount so the pH of the herbicide composition is below the pKa of glyphosate acid.
15. The composition of claim 14 wherein the pH of the herbicide composition is below about 2.6.
16. The composition of claim 14 wherein the herbicide composition does not contain sulfuric acid.
17. The composition of claim 14 comprising acidifying agent selected from the group consisting of: hydrochloric acid, nitric acid, acetic acid, phosphoric acid, polyphosphoric acid, perchloric acid, and combinations thereof.
18. The composition of claim 14 comprising: about 10 to about 100 parts by volume suspension concentrate comprising about 20 to about 50 parts by weight glyphosate acid, about 5 to about 30 total parts by weight of one or more of surfactant, thickener, antifreeze, and antifoam, about 20 to about 60 parts by weight water; and about 1 to about 4 parts by volume aqueous acidifying agent.
19. A method of applying a herbicide composition, the method comprising preparing a herbicide composition comprising a suspension concentrate comprising glyphosate acid, acidifying agent other than sulfuric acid, in an amount so the pH of the herbicide composition is below the pKa of glyphosate acid, and applying the herbicide composition to control plant growth.
20. The method of claim 19 wherein the suspension concentrate comprises from about 25 to about 50 parts by weight glyphosate acid.
21. The method of claim 19 wherein the suspension concentrate comprises glyphosate acid particles suspended in water and surfactant.
22. The method of claim 21 wherein the glyphosate acid particles have an average particle size below about 10 micron.
23. The method of claim 19 wherein the suspension concentrate comprises cationic ethoxylated tallow amine surfactant.
24. The method of claim 19 wherein the pH of the herbicide composition is below about 2.6.
25. The method of claim 19 wherein the acidifying agent is selected from the group consisting of: hydrochloric acid, nitric acid, acetic acid, phosphoric acid, polyphosphoric acid, perchloric acid, and combinations thereof.
26. A method of preparing a suspension concentrate comprising glyphosate acid, the method comprising combining glyphosate acid particles with water and surfactant selected from the group consisting of cationic surfactant, anionic surfactant, short chain alcohol ethoxylate nonionic surfactant, and mixtures thereof, and mixing or agitating the water, glyphosate acid particles, and surfactant, to produce a suspension concentrate.
27. A method of preparing a suspension concentrate comprising glyphosate acid, the method comprising: combining glyphosate acid particles with water, surfactant, and dispersant, wet milling the mixture of glyphosate acid particles, water, surfactant, and dispersant to reduce the size of glyphosate acid particles to a size that can be suspended in the water, surfactant, and dispersant, and using a high speed mixer to mix the water, glyphosate acid particles, surfactant, and dispersant, to produce a suspension concentrate comprising the glyphosate acid particles.
28. The method of claim 27 wherein the glyphosate acid particles are wet milled to an average particle diameter less than 10 microns.
29. The method of claim 27 further comprising adding a thickener to the suspension concentrate comprising the glyphosate acid particles, and mixing.
30. A method of preparing a herbicide composition comprising glyphosate acid, the method comprising preparing a suspension concentrate composition by a method comprising combining glyphosate acid particles with water and one or more of surfactant and dispersant, and mixing or agitating the water, glyphosate acid particles, and one or more of surfactant and dispersant, to produce a suspension concentrate containing the glyphosate acid particles, and combining the suspension concentrate composition with acidifying agent other than sulfuric acid.
31. The method of claim 30 wherein the pH of the herbicide composition is below the pKa of glyphosate acid such that the glyphosate compound is present in the acid form.
32. The suspension concentrate of claim 10 wherein the acidifying agent comprises sulfuric acid.
33. The suspension concentrate of claim 10 wherein the acidifying agent is selected from the group consisting of hydrochloric acid, sulfuric acid, nitric acid, acetic acid, phosphoric acid, polyphosphoric acid, perchloric acid, and combinations thereof.
34. The suspension concentrate of claim 10 wherein the acidifying agent comprises sulfuric acid adduct according to the formula:
Figure imgf000037_0001
wherein X is chalcogen, and each of Rls R2 and R3 is independently selected from hydrogen and organic radicals.
35. The suspension concentrate of claim 10 wherein the acidifying agent comprises an adduct of sulfuric acid and urea.
36. The suspension concentrate of claim 11 comprising acidifying agent.
37. The suspension concentrate of claim 36 wherein the acidifying agent comprises sulfuric acid.
38. The suspension concentrate of claim 36 wherein the acidifying agent is selected from the group consisting of hydrochloric acid, sulfuric acid, nitric acid, acetic acid, phosphoric acid, polyphosphoric acid, perchloric acid, and combinations thereof.
39. The suspension concentrate of claim 36 wherein the acidifying agent comprises a sulfuric acid adduct according to the formula:
Figure imgf000038_0001
wherein X is chalcogen, and each of Rls R2 and R3 is independently selected from hydrogen and organic radicals.
40. The suspension concentrate of claim 36 wherein the acidifying agent comprises an adduct of sulfuric acid and urea.
41. The herbicide composition of claim 14 wherein the acidifying agent comprises a sulfuric acid adduct according to the formula:
Figure imgf000038_0002
wherein X is chalcogen, and each of Ri, R2 and R3 is independently selected from hydrogen and organic radicals.
42. The herbicide composition of claim 14 wherein the acidifying agent is an adduct of sulfuric acid and urea.
PCT/US2002/008952 2001-09-26 2002-03-21 Herbicide compositions comprising suspension concentrate with glyphosate acid, methods of preparation, and methods of use WO2003026429A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
BR0212876-4A BR0212876A (en) 2001-09-26 2002-03-21 Suspension concentrate, herbicidal composition and methods of applying a herbicidal composition and preparing a suspension concentrate and a herbicidal composition.
EP02799541A EP1432316A1 (en) 2001-09-26 2002-03-21 Herbicide compositions comprising suspension concentrate with glyphosate acid, methods of preparation, and methods of use
CA2462127A CA2462127C (en) 2001-09-26 2002-03-21 Herbicide compositions comprising suspension concentrate with glyphosate acid

Applications Claiming Priority (8)

Application Number Priority Date Filing Date Title
US32528901P 2001-09-26 2001-09-26
US32534301P 2001-09-26 2001-09-26
US32534201P 2001-09-26 2001-09-26
US60/325,343 2001-09-26
US60/325,342 2001-09-26
US60/325,289 2001-09-26
US36101602P 2002-02-28 2002-02-28
US60/361,016 2002-02-28

Publications (1)

Publication Number Publication Date
WO2003026429A1 true WO2003026429A1 (en) 2003-04-03

Family

ID=27502307

Family Applications (4)

Application Number Title Priority Date Filing Date
PCT/US2002/008787 WO2003026424A1 (en) 2001-09-26 2002-03-21 Herbicide compound in acid form and acidifying agent
PCT/US2002/008830 WO2003026422A1 (en) 2001-09-26 2002-03-21 Herbicide microemulsion-forming-concentrates, microemulsions, and methods
PCT/US2002/008953 WO2003032729A1 (en) 2001-09-26 2002-03-21 Herbicide compositions comprising imidazolinone acid
PCT/US2002/008952 WO2003026429A1 (en) 2001-09-26 2002-03-21 Herbicide compositions comprising suspension concentrate with glyphosate acid, methods of preparation, and methods of use

Family Applications Before (3)

Application Number Title Priority Date Filing Date
PCT/US2002/008787 WO2003026424A1 (en) 2001-09-26 2002-03-21 Herbicide compound in acid form and acidifying agent
PCT/US2002/008830 WO2003026422A1 (en) 2001-09-26 2002-03-21 Herbicide microemulsion-forming-concentrates, microemulsions, and methods
PCT/US2002/008953 WO2003032729A1 (en) 2001-09-26 2002-03-21 Herbicide compositions comprising imidazolinone acid

Country Status (9)

Country Link
US (10) US7776790B2 (en)
EP (4) EP1432316A1 (en)
JP (2) JP2005503419A (en)
AT (3) ATE332639T1 (en)
AU (3) AU2002306811B2 (en)
BR (3) BR0212876A (en)
CA (4) CA2462127C (en)
DE (3) DE60213114T2 (en)
WO (4) WO2003026424A1 (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2006311623B2 (en) * 2005-11-07 2010-05-13 Los Alamos National Security, Llc Use of prolines for improving growth and/or yield
WO2013164658A1 (en) * 2012-05-02 2013-11-07 Red Surcos, S.A. Glyphosate herbicide composition
US8815773B2 (en) 2009-07-29 2014-08-26 Upl Limited Herbicidal combination
US9045392B2 (en) 2013-03-14 2015-06-02 Los Alamos National Security, Llc Preparation of 4-amino-2,4-dioxobutanoic acid
US9290442B2 (en) 2013-03-14 2016-03-22 Los Alamos National Security, Llc Preparation of 4-amino-2,4-dioxobutanoic acid
US9290443B2 (en) 2013-03-14 2016-03-22 Los Alamos National Security, Llc Preparation of 4-amino-2,4-dioxobutanoic acid
US9963423B2 (en) 2016-01-12 2018-05-08 Millennium Enterprises, Inc. Synthesis of 4-amino-2, 4-dioxobutanoic acid
WO2019215483A1 (en) 2018-05-10 2019-11-14 Red Surcos Colombia Ltda. Herbicide formulation in the form of a microemulsion

Families Citing this family (63)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6093592A (en) * 1983-10-26 1985-05-25 シャープ株式会社 Code registration for indoor security system
US8232230B2 (en) * 2000-12-01 2012-07-31 Helena Holding Company Manufacture and use of a herbicide formulation
CA2462127C (en) * 2001-09-26 2013-04-23 Platte Chemical Co. Herbicide compositions comprising suspension concentrate with glyphosate acid
US9668471B2 (en) * 2003-05-28 2017-06-06 AgQuam LLC Manufacture and use of agricultural spray adjuvants for hard water conditions
DE10343872A1 (en) * 2003-09-23 2005-04-21 Bayer Cropscience Ag Agrochemical suspension concentrates containing azole and/or strobilurin, e.g. the fungicide tebuconazole, containing alkanol ethoxylate penetration promoter and specific polymeric dispersant to increase activity
US8034744B2 (en) * 2003-12-08 2011-10-11 AgQuam LLC Compositions comprising a phosphonic compound, and acids as methods for plant growth and regulatory effects
AU2011203046B2 (en) * 2004-03-03 2011-12-22 Indorama Ventures Oxides Llc Crop oil concentrate adjuvants containing amine surfactants
AU2005218621A1 (en) 2004-03-03 2005-09-15 Huntsman Petrochemical Llc Crop oil concentrate adjuvants containing amine surfactants
EP1722634B2 (en) 2004-03-10 2020-09-02 Monsanto Technology LLC Herbicidal compositions containing n-phosphonomethyl glycine and an auxin herbicide
CA2472806A1 (en) 2004-05-18 2005-11-18 Petro-Canada Compositions and methods for treating turf insect pests and diseases such as fungal infestations
DE102004026938A1 (en) 2004-06-01 2005-12-22 Bayer Cropscience Gmbh Low-foam aqueous formulations for crop protection
US10334842B1 (en) * 2004-09-15 2019-07-02 Solvay Usa, Inc. Agricultural adjuvant compositions, pesticide compositions, and methods for using such compositions
CA2579816C (en) * 2004-09-17 2014-04-29 Monsanto Technology Llc Glyphosate formulations with early burndown symptoms
US8932988B2 (en) * 2004-11-26 2015-01-13 AgQuam LLC Cationic surfactant based adjuvant systems for some herbicides that increase pH, herbicide solubility and performance
US8426341B2 (en) * 2005-05-27 2013-04-23 Helena Holding Company Herbicide formulation
CN101326275B (en) * 2005-10-07 2013-06-05 阿拉巴马大学 Multi-functional ionic liquid compositions
BRPI0711219B1 (en) * 2006-05-26 2016-07-05 Hutsman Petrochemical Corp method for preparing an agricultural composition, and low odor, low volatility solvent for agricultural chemicals
BRPI0715292A2 (en) * 2006-09-22 2013-06-11 Huntsman Spec Chem Corp inhibition of ostwald maturation in chemical formulations
US9357768B2 (en) * 2006-10-05 2016-06-07 Suncor Energy Inc. Herbicidal composition with increased herbicidal efficacy
US20080090780A1 (en) * 2006-10-13 2008-04-17 Pbi/Gordon Corporation Storage stable azadirachtin pesticide formulation
ES2636918T3 (en) 2006-12-06 2017-10-10 Akzo Nobel N.V. Compatibility agents for herbicidal formulations comprising salts of 2,4- (dichlorophenoxy) acetic acid
WO2008068214A2 (en) 2006-12-06 2008-06-12 Akzo Nobel N.V. Alkylamidopropyl dialkylamine surfactants as adjuvants
US8053392B2 (en) * 2007-01-23 2011-11-08 Pbi/Gordon Corporation Auxin acid-catalyzed stable microemulsion pesticide formulation
US9416065B2 (en) * 2007-02-12 2016-08-16 Archer Daniels Midland Company Adjuvants and methods of using them
MX2009008934A (en) 2007-02-26 2009-08-28 Dow Agrosciences Llc Process for the preparation of certain substituted sulfilimines.
US7652048B2 (en) * 2007-05-04 2010-01-26 Troy Corporation Water-based, antimicrobially active, dispersion concentrates
GB2456752B (en) * 2007-12-19 2012-09-19 Rotam Agrochem Int Co Ltd Agrochemical composition and method for preparing the same
RU2488270C2 (en) * 2008-02-05 2013-07-27 Ариста Лайфсайенс Норс Америка, Ллс Solid composition of low-melting active compound
EP2303023B1 (en) 2008-06-26 2016-12-28 Suncor Energy Inc. Improved turfgrass fungicide formulation with pigment
AU2009268127B2 (en) * 2008-07-08 2014-07-03 Akzo Nobel Chemicals International B.V. Surfactant blends useful in agriculture
US9307758B2 (en) 2009-06-19 2016-04-12 Exacto, Inc. Polyacrylamide based agricultural compositions
US9428630B2 (en) 2009-06-19 2016-08-30 Exacto, Inc. Water-in-oil polyacrylamide-based microemulsions and related methods
US9309378B2 (en) 2009-06-19 2016-04-12 Exacto, Inc. Emulsion compositions comprising polyacrylamide copolymer and ethylene oxide—propylene oxide copolymer
WO2011019652A2 (en) 2009-08-10 2011-02-17 Monsanto Technology Llc Low volatility auxin herbicide formulations
WO2011043748A1 (en) * 2009-10-07 2011-04-14 Chrysamed Ki̇mya Sanayi̇ Ve Diş Ti̇caret Li̇mi̇ted Şi̇rketi̇ Composition used in the dissolution and stabilization of pesticide active agents
KR20130109126A (en) 2010-09-09 2013-10-07 선코 에너지 인코포레이티드 Synergistic paraffinic oil and boscalid fungicides
WO2012109639A1 (en) * 2011-02-12 2012-08-16 Ward Paula Marie Herbicidal compositions
AU2012245869B2 (en) * 2011-04-20 2015-12-03 Indorama Ventures Oxides Llc Spray drift reduction agents comprising low hydrophilic-lipophilic balance surfactants
CN103648274B (en) * 2011-05-05 2017-02-08 陶氏益农公司 Stable high strength oil-in-water emulsions
KR20140031966A (en) 2011-06-03 2014-03-13 선코 에너지 인코포레이티드 Paraffinic oil-in-water emulsions for controlling infection of crop plants by fungal pathogens
AU2012328638B2 (en) 2011-10-26 2016-11-17 Monsanto Technology Llc Salts of carboxylic acid herbicides
DK2827714T3 (en) * 2012-03-23 2019-11-11 Dow Agrosciences Llc TANK MIXTURE ADDITIVE CONCENTRATE CONTAINING TRIGLYCERIDE FAT ACID EASTERS AND PROCEDURES FOR USING IT
UY34845A (en) 2012-06-04 2014-01-31 Monsanto Technology Llc ? WATER CONCENTRATED HERBICIDE COMPOSITIONS CONTAINING GLIFOSATE SALTS AND DICAMBA SALTS
US20140005052A1 (en) * 2012-06-28 2014-01-02 Red Surcos S.A. Phytosanitary compositions and spraying products in the form of microemulsions
CN104902746B (en) 2012-11-05 2018-09-21 孟山都技术公司 Low volatility herbicidal composition
HUE040466T2 (en) 2013-02-27 2019-03-28 Monsanto Technology Llc Glyphosate and dicamba tank mixtures with improved volatility
US9464223B2 (en) 2013-03-14 2016-10-11 Flotek Chemistry, Llc Methods and compositions for use in oil and/or gas wells
GB201313803D0 (en) * 2013-08-01 2013-09-18 Omex Agriculture Ltd Fungicidal composition and method
CA2923994C (en) 2013-09-30 2023-08-01 Fmc Corporation Foam formulations and apparatus for delivery
UY36181A (en) * 2014-06-24 2016-09-30 Fmc Corp FORMULATIONS OF FOAMS AND EMULSIONABLE CONCENTRATES
WO2016127027A1 (en) * 2015-02-06 2016-08-11 AgQuam LLC Acid herbicide-containing compositions, precursors, derivatives, and methods
AR104556A1 (en) 2015-05-07 2017-07-26 Nufarm Australia Ltd HERBICIDE COMPOSITION OF BENZOIC ACID
WO2016176743A1 (en) * 2015-05-07 2016-11-10 Nufarm Australia Limited Emulsifiable concentrate comprising picolinic acid herbicide
US10077248B2 (en) * 2015-10-29 2018-09-18 Rotam Agrochem International Company Limited Form of imazapyr, a process for its preparation and use the same
AU2016378184B2 (en) 2015-12-23 2022-04-21 Fmc Corporation In situ treatment of seed in furrow
AU2017280009B2 (en) * 2016-06-20 2020-07-30 AgQuam LLC Methods for managing herbicide vaporization
EP3484288A4 (en) * 2016-07-12 2020-01-08 Monsanto Technology LLC Pesticidal compositions
WO2019056065A1 (en) * 2017-09-21 2019-03-28 Hippocratic Oligo Medicine Corporation Pty Ltd Acetic acid-based herbicide composition
CN109757478A (en) * 2017-11-09 2019-05-17 山东润博生物科技有限公司 A kind of dicamba type missible oil and preparation method thereof
US20210289775A1 (en) * 2018-07-31 2021-09-23 Bayer Aktiengesellschaft Thickener combination for agrochemical (crop protection) formulations with high salt content
CN110934149B (en) * 2018-09-21 2021-03-02 华中师范大学 Microemulsion preparation containing glyphosate herbicide and preparation method and application thereof
AR117186A1 (en) 2020-04-08 2021-07-21 Red Surcos Colombia Ltda PHYTOSANITARY COMPOSITION OF HERBICIDES IN THE FORM OF MICROEMULSION WITH LOW CONTENT OF SURFACTANTS, HIGH COMPATIBILITY IN ULTRA LOW VOLUME SPRAY BROTHS, AND METHOD TO OBTAIN IT
FR3112460B1 (en) * 2020-07-15 2022-08-05 Evergreen Garden Care France Sas HERBICIDE COMPOSITION

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0216126A1 (en) * 1985-08-30 1987-04-01 Union Oil Company Of California Herbicide and method
EP0243522A1 (en) * 1986-04-30 1987-11-04 Union Oil Company Of California Systemic herbicidal compositions and methods of use
EP0357553A2 (en) * 1988-08-30 1990-03-07 Ciba-Geigy Ag Herbicidal mixtures
GB2230955A (en) * 1989-05-02 1990-11-07 Rhone Poulenc Agrochimie Concentrated liquid compositions based on N-phosphonomethylglycine
EP0433577A1 (en) * 1989-11-22 1991-06-26 American Cyanamid Company Herbicidal emulsifiable suspension concentrate compositions
US5189414A (en) * 1986-09-30 1993-02-23 Kabushiki Kaisha Toshiba Network system for simultaneously coupling pairs of nodes
US5288692A (en) * 1982-11-17 1994-02-22 Union Oil Company Of California Systemic herbicides and methods of use
WO1994019941A1 (en) * 1993-03-09 1994-09-15 Kvk Agro A/S A herbicide preparation, a process for producing it and an activating additive for application therewith
WO1999055155A1 (en) * 1998-04-24 1999-11-04 Monsanto Company Concentrate composition of plant treatment compound in acid form
WO2002011536A2 (en) * 2000-08-07 2002-02-14 Helena Chemical Company Manufacture and use of a herbicide formulation

Family Cites Families (79)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US532889A (en) * 1895-01-22 Brake for railway-cars
US3761486A (en) 1971-07-26 1973-09-25 Dow Chemical Co Aminohalopyridyloxy acids and derivatives thereof
US3755339A (en) 1971-07-26 1973-08-28 Dow Chemical Co Esters of aminohalopyridyloxy acids
DE2328192A1 (en) 1972-06-06 1974-01-03 Procter & Gamble HERBICIDAL COMPOSITIONS
US3937826A (en) 1973-05-14 1976-02-10 Pbi-Gordon Corporation Fly killing composition
US4188487A (en) 1977-08-08 1980-02-12 American Cyanamid Company Imidazolinyl benzoic acids, esters and salts and their use as herbicidal agents
DE3125399A1 (en) 1981-06-27 1983-01-13 A. Nattermann & Cie GmbH, 5000 Köln NEW HERBICIDE COMPOSITION, METHOD FOR PRODUCTION AND USE THEREOF
US5411944A (en) 1981-11-05 1995-05-02 Union Oil Company Of California Glyphosate-sulfuric acid adduct herbicides and use
US4445925A (en) 1981-11-05 1984-05-01 Union Oil Company Of California Methods of producing concentrated urea-sulfuric acid reaction products
ATE23093T1 (en) * 1982-07-10 1986-11-15 Nattermann A & Cie HERBICIDE EMULSION CONCENTRATES.
US4994101A (en) 1982-11-17 1991-02-19 Union Oil Company Of California Systemic herbicides and methods of use
US4971630A (en) 1983-07-15 1990-11-20 Pbi/Gordon Corporation Liquid herbicidal composition having extended penetrating and systemic activity
DE3573368D1 (en) 1984-04-27 1989-11-09 Ciba Geigy Ag Herbicidal compositions
CA1225533A (en) 1984-04-30 1987-08-18 Union Oil Company Of California Systemic herbicidal compositions and methods of use
ATE55535T1 (en) 1985-09-27 1990-09-15 American Cyanamid Co PESTICIDES AQUEOUS LIQUID COMPOSITIONS.
DK191386D0 (en) * 1986-04-24 1986-04-24 Koege Kemisk Vaerk emulsifier
US4816060A (en) * 1986-08-15 1989-03-28 American Cyanamid Company Herbicidal aqueous compositions of imidazolinone herbicides
US5668085A (en) 1987-04-29 1997-09-16 Monsanto Company Glyphosate formulations comprising alkoxylated amine surfactants
JPH0618899B2 (en) * 1987-06-30 1994-03-16 品川燃料株式会社 Film containing antibacterial zeolite
EP0334041A3 (en) 1988-02-23 1990-03-28 Mitsubishi Petrochemical Co., Ltd. Herbicidal composition
US5176938A (en) * 1988-11-23 1993-01-05 Plasmacarb Inc. Process for surface treatment of pulverulent material
EP0424873A3 (en) * 1989-10-24 1992-05-27 Tosoh Corporation Method for modifying the surface of a polymer article
US5268352A (en) 1989-11-22 1993-12-07 American Cyanamid Company Herbicidal emulsifiable suspension concentrate compositions
US5317042A (en) 1989-12-11 1994-05-31 Isp Investments Inc. Water-based microemulsion formulations
DK165156C (en) 1989-12-20 1993-03-01 Cheminova Agro As HERBICID FORMULATION CONTAINING GLYPHOSATE ACID
EP0454968A1 (en) 1990-04-30 1991-11-06 American Cyanamid Company Method for enhancing the biological activity of formulations containing solid imidazolinyl benzoic acid esters
US5741502A (en) 1990-07-19 1998-04-21 Helena Chemical Co. Homogeneous, essentially nonaqueous adjuvant compositions with buffering capability
USRE37313E1 (en) 1990-07-19 2001-08-07 Helena Chemical Company Homogeneous, essentially nonaqueous adjuvant compositions with buffering capability
EP0473890A1 (en) 1990-08-28 1992-03-11 American Cyanamid Company Aqueous herbicidal compositions of 2-(2-imidazolin-2-yl)-pyridines and quinolines
IT1243864B (en) * 1990-10-24 1994-06-28 Donegani Guido Ist BODIES FORMED IN POLYMERIC MATERIAL WITH IMPROVED SURFACE CHARACTERISTICS AND PROCESS FOR THEIR OBTAINING.
US5270286A (en) 1991-01-31 1993-12-14 American Cyanamid Company Herbicidal emulsifiable concentrate compositions of imidazolinone herbicides
CA2097707A1 (en) 1991-02-12 1992-08-13 Kolazi S. Narayanan Stabilization of microemulsions using hydrophobic acid buffers
GB9109599D0 (en) 1991-05-03 1991-06-26 Dow Chemical Co Herbicidal compositions with reduced phytotoxicity
US5498773A (en) 1991-05-03 1996-03-12 Dowelanco Herbicidal compositions with increased crop safety
GB9111974D0 (en) 1991-06-04 1991-07-24 Ici Plc Novel process
US5221319A (en) 1991-08-16 1993-06-22 Pbi-Gordon Corporation Dry, water-soluble, substituted phenoxy and/or benzoic acid herbicidal compositions and method of preparing same
US5328889A (en) 1992-07-10 1994-07-12 Pbi-Gordon Corporation Dry, water-soluble, substituted phenoxy and/or benzoic acid herbicides and method of preparing same
US5280008A (en) 1991-08-16 1994-01-18 Pbi-Gordon Corporation Dry, water-soluble powder, substituted heterocyclic acid or substituted phenol herbicidal compositions, and method of preparing same
JPH06509805A (en) 1991-08-16 1994-11-02 ピービーアイ/ゴードン・コーポレーション Dry, water-soluble, substituted phenoxy acid and/or substituted benzoic acid herbicides and processes for their production
TW280760B (en) 1992-04-28 1996-07-11 Du Pont
GB2267825B (en) 1992-05-26 1995-08-30 Dowelanco Herbicidal aqueous-based microemulsion compositions
US5416067A (en) 1992-07-10 1995-05-16 Pbi - Gordon Corporation Dry, water-soluble, substituted phenoxy and/or benzoic acid herbicides and method of preparing same
US5558806A (en) * 1992-07-23 1996-09-24 Osi Specialties, Inc. Surfactant blend of a polyalkleneoxide polysiloxane and an organic compound having a short chain hydrophobic moiety
US5283086A (en) * 1992-12-23 1994-02-01 The University Of Western Ontario Plasma treatment of polymer powders
US5565409A (en) 1993-04-02 1996-10-15 Monsanto Company Liquid concentrated herbicidal microemulsion compositions comprising glyphosate and either oxyfluorfen or acifluorfen
US5707928A (en) 1993-09-28 1998-01-13 American Cyanamid Company Emulsifiable suspension concentrate compositions of imidazolinyl benzoic acids, esters and salts thereof, and dinitroaniline herbicides
DK0645083T3 (en) * 1993-09-28 1999-09-20 American Cyanamid Co Emulsifiable suspension concentrates of imidazolinylbenzoic acids, esters and salts thereof and dinitroaniline herbicides
US5416036A (en) * 1993-10-04 1995-05-16 United Microelectronics Corporation Method of improvement ESD for LDD process
WO1996008150A1 (en) 1994-09-15 1996-03-21 Akzo Nobel N.V. Aqueous pesticidal microemulsion compositions
US5538938A (en) * 1994-10-14 1996-07-23 Monsanto Company Stable emulsion flowable formulation of a 2-chloroacetamide herbicide and an imidazolinone herbicide
US5696024A (en) * 1995-06-06 1997-12-09 American Cyanmid Herbicidal water soluble granular compositions
US5772640A (en) * 1996-01-05 1998-06-30 The Trustees Of Columbia University Of The City Of New York Triclosan-containing medical devices
FR2744649B1 (en) * 1996-02-12 1998-04-10 Conte METHOD FOR INCREASING THE WETABILITY OF A POROUS BODY AND DEVICE FOR IMPLEMENTING THE PROCESS
AU719494B2 (en) 1996-06-28 2000-05-11 Novartis Ag Pesticidal compositions
US5859086A (en) * 1996-08-07 1999-01-12 Competitive Technologies Of Pa, Inc. Light directed modification fluoropolymers
HU227713B1 (en) 1996-10-25 2012-01-30 Monsanto Technology Llc Compositions and process for treating plants with exogenous chemicals
AU708918B2 (en) 1997-01-28 1999-08-19 Syngenta Participations Ag Herbicidal synergistic composition and method of weed control
US5877112A (en) 1997-08-27 1999-03-02 Helena Chemical Company Agricultural formulation
US6127317A (en) 1997-09-17 2000-10-03 American Cyanamid Company Concentrated, aqueous herbicidal compositions containing an imidazolinyl acid salt and a glyphosate salt
US6069115A (en) 1997-11-12 2000-05-30 Rhone-Poulenc Agrochimie Method of controlling weeds in transgenic crops
US6156705A (en) 1997-12-04 2000-12-05 Henkel Corporation Use of fatty alcohol polyalkoxy alkyl ethers in agricultural formulations
ITTO980048A1 (en) 1998-01-20 1999-07-20 Ipici Spa HERBICIDE COMPOSITIONS, PROCEDURES FOR THEIR PREPARATION AND USES
ID26936A (en) 1998-03-09 2001-02-22 Monsanto Co HERBISIDE COMPOSITION CONCENTRATE
JP4230607B2 (en) 1998-07-24 2009-02-25 株式会社ショーワ Damping damper with preload
US6235300B1 (en) 1999-01-19 2001-05-22 Amway Corporation Plant protecting adjuvant containing topped or peaked alcohol alkoxylates and conventional alcohol alkoxylates
US6232272B1 (en) 1999-02-02 2001-05-15 Helena Chemical Company Manufacture and use of herbicide chlorinated phenoxy formulation
AUPQ017699A0 (en) 1999-05-05 1999-05-27 Victorian Chemicals International Pty Ltd Agrochemical composition
US6369001B1 (en) * 1999-08-11 2002-04-09 Monsanto Technology, Llc Microemulsion coformulation of a graminicide and a water-soluble herbicide
US6939555B2 (en) 2000-01-21 2005-09-06 Helena Holding Company Manufacture and use of an deposition aid
AR026824A1 (en) 2000-01-21 2003-02-26 Ishihara Sangyo Kaisha HERBICIDE MICROEMULSION
US20010034304A1 (en) 2000-01-21 2001-10-25 Greg Volgas Manufacture and use of an deposition aid
US6187715B1 (en) 2000-02-16 2001-02-13 Isp Investments Inc. Water-based microemulsions of a lower alkyl ester of quinoxalinyl herbicide
US8232230B2 (en) 2000-12-01 2012-07-31 Helena Holding Company Manufacture and use of a herbicide formulation
GB0103761D0 (en) 2001-02-15 2001-04-04 Syngenta Ltd Agrochemical formulation
US6831038B2 (en) 2001-02-20 2004-12-14 Helena Holding Company Agricultural formulation
CA2462127C (en) * 2001-09-26 2013-04-23 Platte Chemical Co. Herbicide compositions comprising suspension concentrate with glyphosate acid
US20030091767A1 (en) * 2001-11-02 2003-05-15 Podhajny Richard M. Anti-microbial packaging materials and methods for making the same
WO2003103396A1 (en) 2002-06-11 2003-12-18 Helena Chemical Company Research Extension And Service Center Manufacture and use of a herbicide formulation
US9668471B2 (en) 2003-05-28 2017-06-06 AgQuam LLC Manufacture and use of agricultural spray adjuvants for hard water conditions

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5288692A (en) * 1982-11-17 1994-02-22 Union Oil Company Of California Systemic herbicides and methods of use
EP0216126A1 (en) * 1985-08-30 1987-04-01 Union Oil Company Of California Herbicide and method
EP0243522A1 (en) * 1986-04-30 1987-11-04 Union Oil Company Of California Systemic herbicidal compositions and methods of use
US5189414A (en) * 1986-09-30 1993-02-23 Kabushiki Kaisha Toshiba Network system for simultaneously coupling pairs of nodes
EP0357553A2 (en) * 1988-08-30 1990-03-07 Ciba-Geigy Ag Herbicidal mixtures
GB2230955A (en) * 1989-05-02 1990-11-07 Rhone Poulenc Agrochimie Concentrated liquid compositions based on N-phosphonomethylglycine
EP0433577A1 (en) * 1989-11-22 1991-06-26 American Cyanamid Company Herbicidal emulsifiable suspension concentrate compositions
WO1994019941A1 (en) * 1993-03-09 1994-09-15 Kvk Agro A/S A herbicide preparation, a process for producing it and an activating additive for application therewith
WO1999055155A1 (en) * 1998-04-24 1999-11-04 Monsanto Company Concentrate composition of plant treatment compound in acid form
WO2002011536A2 (en) * 2000-08-07 2002-02-14 Helena Chemical Company Manufacture and use of a herbicide formulation

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; S.L.SHERRICK ET AL.: "Effects of adjuvants and environment during plant development on glyphosate adsorption and translocation in field bindweed (Convolvulus arvensis)", XP002211986, retrieved from STN-INTERNATIONAL Database accession no. 106:14601 CA *
WEED SCI., vol. 34, no. 6, 1986, pages 811 - 816 *
WYRILL J B ET AL: "GLYPHOSATE TOXICITY TO COMMON MILKWEED AND HEMP DOGBANE AS INFLUENCED BY SURFACTANTS", WEED SCIENCE, WEED SCIENCE SOCIETY OF AMERICA, CHAMPAIGN, IL, US, vol. 25, no. 3, 1 May 1977 (1977-05-01), pages 275 - 287, XP002034447, ISSN: 0043-1745 *

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2006311623B2 (en) * 2005-11-07 2010-05-13 Los Alamos National Security, Llc Use of prolines for improving growth and/or yield
US8551917B2 (en) * 2005-11-07 2013-10-08 Los Alamos National Security, Llc Use of prolines for improving growth and/or yield
US8802595B2 (en) 2005-11-07 2014-08-12 Los Alamos National Security, Llc Use of prolines for improving growth and/or yield
US8815773B2 (en) 2009-07-29 2014-08-26 Upl Limited Herbicidal combination
WO2013164658A1 (en) * 2012-05-02 2013-11-07 Red Surcos, S.A. Glyphosate herbicide composition
US9045392B2 (en) 2013-03-14 2015-06-02 Los Alamos National Security, Llc Preparation of 4-amino-2,4-dioxobutanoic acid
US9290442B2 (en) 2013-03-14 2016-03-22 Los Alamos National Security, Llc Preparation of 4-amino-2,4-dioxobutanoic acid
US9290443B2 (en) 2013-03-14 2016-03-22 Los Alamos National Security, Llc Preparation of 4-amino-2,4-dioxobutanoic acid
US9963423B2 (en) 2016-01-12 2018-05-08 Millennium Enterprises, Inc. Synthesis of 4-amino-2, 4-dioxobutanoic acid
WO2019215483A1 (en) 2018-05-10 2019-11-14 Red Surcos Colombia Ltda. Herbicide formulation in the form of a microemulsion
CN112399796A (en) * 2018-05-10 2021-02-23 睿舒柯哥伦比亚有限公司 Herbicidal formulations in the form of microemulsions

Also Published As

Publication number Publication date
AU2002306811B2 (en) 2008-05-15
US20030153461A1 (en) 2003-08-14
WO2003026424A1 (en) 2003-04-03
DE60213114T2 (en) 2007-02-15
DE60222573D1 (en) 2007-10-31
DE60222573T2 (en) 2008-06-12
US6906004B2 (en) 2005-06-14
ATE362314T1 (en) 2007-06-15
CA2462127A1 (en) 2003-04-03
CA2462124C (en) 2009-12-08
US7094735B2 (en) 2006-08-22
WO2003032729A1 (en) 2003-04-24
BR0212876A (en) 2004-09-14
CA2462955C (en) 2010-02-09
EP1432316A1 (en) 2004-06-30
US7776790B2 (en) 2010-08-17
US9237746B2 (en) 2016-01-19
BR0212871B1 (en) 2014-10-14
JP2005503419A (en) 2005-02-03
EP1432314A1 (en) 2004-06-30
EP1432311A1 (en) 2004-06-30
BR0212871A (en) 2004-10-13
EP1432314B1 (en) 2007-05-16
EP1432307B1 (en) 2007-09-19
BR0212870A (en) 2004-10-13
CA2462122C (en) 2010-02-09
EP1432311B9 (en) 2008-08-27
ATE332639T1 (en) 2006-08-15
DE60220174D1 (en) 2007-06-28
US20030148889A1 (en) 2003-08-07
US20050170967A1 (en) 2005-08-04
CA2462127C (en) 2013-04-23
EP1432307A1 (en) 2004-06-30
DE60213114D1 (en) 2006-08-24
US20040127364A1 (en) 2004-07-01
DE60220174T2 (en) 2008-01-17
EP1432311B1 (en) 2006-07-12
AU2002254345B2 (en) 2007-07-05
US20030144147A1 (en) 2003-07-31
US20100184599A1 (en) 2010-07-22
US20140323309A1 (en) 2014-10-30
JP2005512963A (en) 2005-05-12
CA2462122A1 (en) 2003-04-03
CA2462124A1 (en) 2003-04-03
US6703346B2 (en) 2004-03-09
US20030153462A1 (en) 2003-08-14
US6803345B2 (en) 2004-10-12
CA2462955A1 (en) 2003-04-24
US8759256B2 (en) 2014-06-24
WO2003026422A1 (en) 2003-04-03
US20060205601A1 (en) 2006-09-14
ATE373422T1 (en) 2007-10-15
AU2002255869B2 (en) 2008-06-05
US20050137091A1 (en) 2005-06-23

Similar Documents

Publication Publication Date Title
US7776790B2 (en) Herbicide compositions comprising suspension concentrate with glyphosate acid, methods of preparation, and methods of use
AU2002254345A1 (en) Herbicide compositions comprising imidazolinone acid
US20190075799A1 (en) Glyphosate Salt Herbicidal Composition
EP0820231B1 (en) Glyphosate formulations containing etheramine surfactants
AU2002255869A1 (en) Herbicide compound in acid form and acidifying agent
EP2677866B1 (en) New uses of choline chloride in agrochemical formulations
AU2002306811A1 (en) Herbicide microemulsion-forming-concentrates, microemulsions, and methods
CA3004762C (en) Flumioxazin compositions
WO2003059068A1 (en) High-strength low-viscosity agricultural formulations
AU2002306827A1 (en) Herbicide compositions comprising suspension concentrate with glyphosate acid, methods of preparation, and methods of use

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BY BZ CA CH CN CO CR CU CZ DE DM DZ EC EE ES FI GB GD GE GH HR HU ID IL IN IS JP KE KG KP KR LC LK LR LS LT LU LV MA MD MG MN MW MX MZ NO NZ OM PH PL PT RU SD SE SG SI SK SL TJ TM TN TR TZ UA UG UZ VN YU ZA ZM

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ UG ZM ZW AM AZ BY KG KZ RU TJ TM AT BE CH CY DE DK FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GQ ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
WWE Wipo information: entry into national phase

Ref document number: 2462127

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 2002306827

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 2002799541

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 2002799541

Country of ref document: EP

NENP Non-entry into the national phase

Ref country code: JP

WWW Wipo information: withdrawn in national office

Country of ref document: JP