[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

US20120283098A1 - Stable high strength oil-in-water emulsions - Google Patents

Stable high strength oil-in-water emulsions Download PDF

Info

Publication number
US20120283098A1
US20120283098A1 US13/463,848 US201213463848A US2012283098A1 US 20120283098 A1 US20120283098 A1 US 20120283098A1 US 201213463848 A US201213463848 A US 201213463848A US 2012283098 A1 US2012283098 A1 US 2012283098A1
Authority
US
United States
Prior art keywords
oil
water
composition
emulsion
glyphosate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US13/463,848
Inventor
Hong Zhang
Holger Tank
Franklin N. Keeney
Mei Li
Marco A. Tavares Do Nascimento
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Corteva Agriscience LLC
Original Assignee
Dow AgroSciences LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dow AgroSciences LLC filed Critical Dow AgroSciences LLC
Priority to US13/463,848 priority Critical patent/US20120283098A1/en
Publication of US20120283098A1 publication Critical patent/US20120283098A1/en
Priority to US14/510,289 priority patent/US11058108B2/en
Abandoned legal-status Critical Current

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
    • 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
    • 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
    • A01N25/30Biocides, 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 characterised by the surfactants
    • 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
    • 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

Definitions

  • a common method of herbicidal treatment in agricultural endeavors is to treat a field to remove or control unwanted vegetation in preparation for planting a crop plant or seed, a method otherwise known as a “burndown” herbicide treatment.
  • single herbicides typically lack the weed control spectrum, e.g., the range of weed species effectively controlled by the herbicide, to fully control the diversity of weeds in such an environment and therefore, it is common to apply two or more herbicides simultaneously in order to achieve the desired spectrum of control with the burndown treatment.
  • the herbicides are often sold separately and mixed in a spray tank by the end user.
  • a more convenient way to deliver these herbicides is to formulate them into a single pre-mix concentrate that can easily be measured and diluted in water by the end user prior to application by spraying.
  • Glyphosate containing compositions are of particular interest in burndown herbicide applications due to their wide spectrum of weed control. These compositions are made more useful by expanding their spectrum of weed control even further by the addition of an oil soluble herbicide.
  • An oil-in-water emulsion (EW) composition may be used to combine an oil soluble herbicide and a water soluble herbicide, such as a glyphosate, into a pre-mix herbicide concentrate where droplets of oil are stabilized by surfactant emulsifiers as a discrete phase and are uniformly dispersed in water as a continuous phase.
  • Oil-in-water emulsions can have stability issues caused by one or more factors. Interactions or reactions of an ingredient in the aqueous phase with component(s) of the dispersed oil phase include, but are not limited to, crystal formation and growth due to Ostwald ripening of an oil phase component or an aqueous phase component, or chemical degradation of ingredients in either the oil phase or the aqueous phase. These degradations may be caused by the presence of one or more components in the oil-in-water emulsion and can lead to formulation instability.
  • Migration of water into the oil phase and contact with the active ingredient dissolved in the oil phase or migration of the active ingredient into the water phase or to the oil-water interface can lead to one or more of active ingredient hydrolysis, crystal formation or Ostwald ripening with possible formulation instability or unsuitability for agricultural spray applications.
  • a high ionic strength aqueous solution such as, for example, a water solution containing a soluble glyphosate salt.
  • the high ionic strength aqueous solution can destabilize the emulsion leading to coalescence of the oil droplets into larger sized oil droplets which may ultimately cause the emulsion to separate into two liquid layers.
  • This undesired phenomenon has been attributed to the electrolyte decreasing the electrostatic repulsive force between the dispersed droplets, thus causing the droplets to agglomerate.
  • This stability issue becomes more severe in a high load emulsion system, and at high temperature extremes.
  • High-strength formulations are desirable for a variety of economic and environmental reasons. For example, it is desirable to provide a high-strength concentrate in order to reduce shipping and handling costs and to reduce the amount of packaging material that must be disposed after use of the product.
  • the high-strength concentrates should be stable and retain potency during storage and shipping.
  • the high-strength concentrate should be a homogeneous liquid emulsion that is stable at temperatures at least as high as about 50 ° C. and should not exhibit any precipitation of solids at temperatures as low as about 0 ° C.
  • a stable high-strength herbicidal oil-in-water emulsion includes:
  • a discontinuous oil phase comprising, with respect to the oil-in-water emulsion, from about 25 grams active ingredient per liter (g ai/L) to about 300 g ai/L of at least one oil soluble herbicide active ingredient and from 0 grams per liter (g/L) to about 300 g/L of a water immiscible organic solvent;
  • a continuous aqueous phase comprising, with respect to the oil-in-water emulsion, from about 260 g ai/L to about 570 g ai/L of a water soluble salt of glyphosate and from about 200 g/L to about 500 g/L of water;
  • emulsifying surfactants with at least one having a hydrophile lipophile balance (HLB) value of about 13 to about 16 and at least one having an HLB value of about 22 to about 29 and each having a molecular weight (mw) of about 5000 or higher, with the combined emulsifying surfactants comprising, with respect to the oil-in-water emulsion, from about 1 g/L to about 200 g/L.
  • HLB hydrophile lipophile balance
  • a method of preparing a stable high-strength herbicidal oil-in-water emulsion composition includes:
  • a) preparing a discontinuous oil phase comprising, with respect to the oil-in-water emulsion, from about 25 grams active ingredient per liter (g ai/L) to about 300 g ai/L of at least one oil soluble herbicide active ingredient and from 0 grams per liter (g/L) to about 300 g/L of a water immiscible organic solvent;
  • a continuous aqueous phase comprising, with respect to the oil-in-water emulsion, from about 260 g ai/L to about 570 g ai /L of a water soluble salt of glyphosate and from about 200 g/L to about 500 g/L of water, and at least two non-ionic EO/PO block copolymer emulsifying surfactants with at least one having a hydrophile lipophile balance (HLB) value of about 13 to about 16 and at least one having an HLB value of about 22 to about 29 and with each having a molecular weight (mw) of about 5000 or higher, with the combined emulsifying surfactants comprising, with respect to the oil-in-water emulsion, from about 1 g/L to about 200 g/L; and
  • HLB hydrophile lipophile balance
  • a high-strength, herbicidal oil-in-water emulsion pre-mix composition comprising a dispersed oil phase containing at least one oil soluble herbicide and a water immiscible organic solvent, a continuous aqueous phase containing a water soluble salt of glyphosate, and at least two non-ionic EO/PO block copolymer emulsifying surfactant, one having an hydrophile lipophile balance (HLB) value of about 13 to about 16 and the other having an HLB value of about 22 to about 29, both having a molecular weight (mw) of about 5000 or higher is disclosed.
  • the composition may optionally include additional active ingredients and inert formulation ingredients.
  • the oil soluble herbicide active ingredient contained in the discontinuous oil phase of the compositions disclosed herein may generally be selected from the class of synthetic auxin and lipid synthesis inhibitor (ACCase inhibitors) herbicides.
  • Preferred herbicide active ingredients include, but are not limited to, oil soluble derivatives of carboxylic acid herbicides, such as esters of the following: benzoic acid herbicides, such as dicamba; phenoxyalkanoic acid herbicides, such as 2,4-D, MCPA and 2,4-DB; pyridinecarboxylic acid herbicides, such as aminopyralid, picloram and clopyralid; pyridinyloxyalkanoic acid herbicides such as fluroxypyr and triclopyr; pyrimidinecarboxylic acids, such as aminocyclopyrachlor; and, esters of the aryloxyphenoxypropionic acids, such as cyhalofop, clodinafop, diclofop, fenoxaprop, flu
  • Preferred oil-soluble herbicide active ingredients also include cyclohexanediones, such as cycloxydim, sethoxydim, tralkoxydim and the like.
  • the oil soluble herbicide active ingredient of the compositions disclosed herein generally has a water solubility of less than about 3000 parts per million (ppm) and preferably less than about 1000 ppm.
  • the oil soluble herbicide active ingredient comprises, with respect to the oil-in-water emulsion, from about 25 g ai/L to about 300 g ai/L.
  • the water immiscible organic solvent of the compositions disclosed herein generally has a water solubility of less than about 1000 ppm and may include, but is not limited to, one or more of petroleum fractions or hydrocarbons such as mineral oil, kerosene, paraffinic oils, mixed naphthalene and alkyl naphthalene fractions, aromatic solvents, particularly alkyl substituted benzenes such as xylene or propylbenzene fractions, and the like; heavy aromatic solvent naphtha such as Aromatic 150 fluid (Exxon Mobil Chemical; Houston, Tex.), dialkyl amides of carboxylic acids, particularly the dimethyl amides of fatty acids such as the dimethyl amide of caprylic acid and the like; vegetable, animal, algae or seed oils such as soybean oil, rape seed oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cotton seed oil, linseed oil, palm oil, peanut oil, safflower oil, sesame oil
  • Preferred water immiscible organic solvents include one or more of petroleum fractions or hydrocarbons such as mineral oil, paraffinic oils and aromatic solvents like xylene, propylbenzene fractions, alkyl naphthalene fractions, and the like; dialkyl amides of carboxylic acids, particularly the dimethyl amides of fatty acids such as the dimethyl amide of caprylic acid and the like; vegetable or seed oils such as soybean oil, rape seed oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cotton seed oil, linseed oil, palm oil, peanut oil, safflower oil, sesame oil, tung oil and the like; and C 1 -C 5 esters of vegetable or seed oils and the like.
  • the water immiscible organic solvent may comprise, with respect to the oil-in-water emulsion, from about 0 g/L to about 300 g/L, preferably from about 10 g/L to about 300 g/L.
  • Optional ingredients that may be added to the discontinuous oil phase described herein include emulsion stabilizers such as, but not limited to, one or more low molecular weight homopolymers ( ⁇ 5000 mw) of the following: polyolefins, such as polybutadiene, polyisoprene, poly(substituted butadienes), such as poly(2-t-butyl-1,3-butadiene), polyethylene, chlorinated polyethylene, polypropylene, polybutene, polyisobutene, polycyclopentylethylene and polycyclolhexylethylene; polyacrylates, including polyalkylacrylates and polyarylacrylates; polymethacrylates, including polyalkylmethacrylates and polyarylmethacrylates; polydisubstituted esters, such as poly(di-n-butylitaconate) and poly(amylfumarate); polyvinylethers, such as poly(butoxyethylene) and poly(benzyloxy
  • the continuous aqueous phase of the compositions disclosed herein comprises water as the solvent medium and a water soluble salt of glyphosate.
  • water in the aqueous phase of the emulsion formulation is used to dissolve the salt of glyphosate and any other water soluble ingredients and to balance the final composition.
  • the continuous aqueous phase of the compositions disclosed herein may comprise, with respect to the oil-in-water emulsion, from about 200 g/L to about 500 g/L, preferably from about 200 g/L to about 400 g/L of water.
  • the water soluble salt of glyphosate contained in the continuous aqueous phase of the compositions disclosed herein may comprise one or more of an organo ammonium salt and the potassium salt of glyphosate.
  • Suitable water soluble organo ammonium salts of glyphosate include, but are not limited to, dimethyl ammonium, isopropyl ammonium, monoethanol ammonium and the N,N,N,N-trimethylethanol ammonium (choline) salt of glyphosate.
  • the water soluble salt of glyphosate may comprise, with respect to the oil-in-water emulsion, from about 260 g ai/L to about 570 g ai/L, preferably from about 260 g ai/L to about 450 g ai/L.
  • compositions described herein also include at least two non-ionic EO/PO block copolymer emulsifying surfactants with a hydrophile lipophile balance (HLB) value of 13 or higher and a molecular weight (mw) of about 5000 or higher.
  • HLB hydrophile lipophile balance
  • mw molecular weight
  • the utility of non-ionic surfactants in emulsifying an oil-water mixture may in part be predicted by the Hydrophile-Lipophile Balance (HLB) values of the surfactants.
  • the HLB value of a surfactant estimates the balance between the oil soluble and water soluble moieties in a surface active molecule (i.e., a surfactant).
  • a more oil-soluble emulsifier will have a lower HLB value (less than about 7) and a more water-soluble emulsifier will have a larger HLB value (greater than about 7).
  • the HLB approach is a useful method to select an emulsifier for a particular application and is more fully described in “The HLB System” an online publication available from the crodalubricants.com website at the following link:
  • the non-ionic EO/PO block copolymer emulsifying surfactants of the compositions disclosed herein include at least one surfactant with an HLB value of about 13 to about 16 and at least one surfactant with an HLB value of about 22 to about 29, with the surfactants having a molecular weight of a least about 5000.
  • the EO/PO block copolymer emulsifying surfactants described herein include both di- and tri-block co-polymers of ethylene oxide (EO) and propylene oxide (PO).
  • Preferred non-ionic EO/PO block copolymer surfactants of the compositions disclosed herein include, but are not limited to, Pluronic® L35, L44, L64, P65, P75, P84, P85, P104, P105, F77, F87, F88, F68, F68 LF, F98, F108, F127, 17R8 and 25R8; Tetronic® 704, 707, 904, 1104, 1107, 1307, 1504, 1508, 50R8 and 90R8; Macol® 15-20; Toximul® 8323 and 8323/33; Step-Flow® 26, 26F and 1500; Synperonic® PE 30/40, PE 30/80 and PE 39/70; Pegol® 10R8, 17R8, 25R8, F-68LF, F-108, F-127, L-10, L-35, L-44, P-65, P-75 and P-85; Antarox® 724/P, T-Det® BP-1, EPO-64 and EPO-104; A
  • the non-ionic EO/PO block copolymer emulsifying surfactants of the compositions disclosed herein may comprise, with respect to the oil-in-water emulsion, from about 1 g/L to about 200 g/L, preferably from about 1 g/L to about 100 g/L.
  • compositions described herein may optionally contain additional water soluble herbicide active ingredients if they cause no incompatibility or active ingredient stability issues to other ingredients of the composition.
  • water soluble herbicide active ingredients may be selected from, but are not limited to, alkali metal salts or amine salts of benzoic acids, phenoxyalkanoic acids, pyridinecarboxylic acids, pyrimidinecarboxylic acids and pyridinyloxycarboxylic acids such as, dicamba, 2,4-D, MCPA, 2,4-DB, aminopyralid, aminocyclopyrachlor, picloram, clopyralid, fluroxypyr and triclopyr, and alkali metal salts of bromoxynil and ioxynil.
  • the amines are comprised of primary, secondary or tertiary alkylamines, alkanolamines, alkylalkanolamines or alkoxyalkanolamines wherein the alkyl and alkanol groups are saturated and contain C 1 -C 4 alkyl groups individually.
  • the alkali metals are comprised of sodium and potassium.
  • compositions described herein may optionally contain inert formulation ingredients such as, but not limited to, adjuvants, antifoam agents, dispersants, surfactants, spray drift reduction agents, stabilizers and wetting agents.
  • inert formulation ingredients such as, but not limited to, adjuvants, antifoam agents, dispersants, surfactants, spray drift reduction agents, stabilizers and wetting agents.
  • These optional inert ingredients may include surfactants conventionally used in the art of formulation that are described, inter alia, in “McCutcheon's Detergents and Emulsifiers Annual,” MC Publishing Corp., Ridgewood, N.J., 1998 and in the “Encyclopedia of Surfactants,” Vol. I-III, Chemical Publishing Co., N.Y., 1980-81.
  • Adjuvants that are particularly well-suited for use in the compositions disclosed herein may include one or more of: alkylamine surfactants having 8 to 22 carbon atoms such as Armeen® DMTD and Duomeen® TTM; alkoxylated alkylamine surfactants having 8 to 22 carbon atoms and a total of 1-20 alkylene oxide groups such as Ethomeen® C/12, Ethomeen® T/12, Ethoduomeen® T/13 and Propomeen® T/12; etheramine surfactants such as Tomah® E-14-2, Tomah® E-14-5 and Tomah® PA-17; amine oxide surfactants such as Aromox C/12, Aromox DMC, Ammonyx® LO, Ammonyx® CDO and Tomah®AO-14-2; amidoamine surfactants such as Adsee C80W; quaternary ammonium surfactants such as Arquad® T/50, Arquad° APA-E, Duoquad° T/50, Ethoqua
  • compositions disclosed herein provide a high-strength herbicidal oil-in-water emulsion composition that is storage stable at high temperatures. That is, the composition forms a stable, homogeneous emulsion that does not exhibit coalescence under the storage conditions. More preferably, the composition described herein is stable at temperatures of greater than or equal to about 40° C. for a period of at least 4 weeks, more preferably, at temperatures greater than or equal to about 54° C. for a period of at least about 4 weeks.
  • the high-strength oil-in-water emulsion composition described herein also does not exhibit separation or precipitation (or crystallization) of any of the components at low temperatures.
  • the composition remains a homogeneous emulsion at temperatures below about 20° C., more preferably at temperatures below about 10° C. and most preferably at a temperature equal to or less than about 5° C. for a period of at least about 4 weeks.
  • the aqueous phase is prepared by mixing the water with water soluble or water dispersible ingredients including, but not limited to, water soluble or water dispersible dispersing or emulsifying surfactants, water soluble active ingredients and optionally, other inert ingredients such as thickeners, pH buffers, wetting agents, antifreeze agents, antifoam agents, biocides, etc.
  • the oil phase is prepared by mixing the oil-soluble emulsifying surfactants with oil miscible or soluble ingredients, including but not limited to, water immiscible organic solvents and oil soluble active ingredients.
  • Emulsion droplet sizes can be, for example, between 0.1 ⁇ m and 5 ⁇ m, between 0.1 ⁇ m and 4 ⁇ m, 0.1 ⁇ m and 3 ⁇ m, 0.1 ⁇ m and 2 ⁇ m, or 0.1 ⁇ m and 1 ⁇ m.
  • An example of a stable, high-strength oil-in-water emulsion composition described herein in which coalescence of the dispersed oil phase and crystallization and Oswald ripening of an oil soluble active ingredient is retarded comprises:
  • a discontinuous oil phase comprising, with respect to the oil-in-water emulsion, from about 25 g ai/L to about 300 g ai/L of fluroxypyr-meptyl and from about 1 g/L to about 300 g/L of naphthalene depleted Aromatic 150 fluid;
  • a continuous aqueous phase comprising, with respect to the oil-in-water emulsion, from about 310 g ai/L to about 570 g ai/L of glyphosate dimethyl ammonium and from about 200 g/L to about 500 g/L of water;
  • HLB hydrophile lipophile balance
  • compositions and use of oil-in-water emulsions in combination with one or more additional compatible ingredients may include, for example, one or more other pesticides, dyes, and any other additional ingredients providing functional utility, such as, for example, stabilizers, compatibility agents, fragrants, viscosity-modifying additives, suspension aids, dispersants, and freeze-point depressants.
  • aqueous herbicidal compositions described herein may optionally be diluted in an aqueous spray mixture for agricultural application such as for burndown weed control in crop fields prior to planting.
  • Such compositions are typically diluted with an inert carrier, such as water, before application.
  • the diluted compositions which are usually applied to weeds, the locus of weeds or the locus of where weeds may eventually emerge, generally contain about 0.0001 to about 1 weight percent active ingredient and preferably contain about 0.001 to about 0.05 weight percent active ingredient.
  • the compositions disclosed herein can be applied to weeds or their locus by the use of conventional ground or aerial sprayers, by addition to irrigation water and by other conventional means known to those skilled in the art.
  • compositions described herein may be applied in conjunction with one or more other herbicides to control a wider variety of undesirable vegetation.
  • the presently claimed compositions can be formulated with the other herbicide or herbicides as premix concentrates, tank mixed with the other herbicide or herbicides for spray application or applied sequentially with the other herbicide or herbicides in separate spray applications.
  • a glyphosate DMA salt concentrate was prepared by mixing 247.4 g glyphosate acid technical (purity 97%) with 1.1 molar equivalents of dimethylamine aqueous solution (40% in water) to form a homogeneous clear solution at ambient temperature. To the glyphosate DMA solution were then added 31.2 g of Agnique® PG 8107-U (Agnique is a registered trademark of Cognis) and 154.9 g of water to achieve a concentration of 608 g ai/L [480 grams acid equivalent per liter (g ae/L)] of glyphosate DMA.
  • An oil phase was prepared by dissolving 35.6 g of fluroxypyr MHE (purity 97.1%) in 53.4 g of Aromatic 150 ND fluid (ExxonMobil Chemical Company; Houston, Tex.) containing 13.7 g of Pluronic® F68 LF
  • Soprophor® 796/P Soprophor is a registered trademark of Rhodia Inc
  • Indopol® H15 Indopol is a registered trademark of INEOS Oligomers
  • Example A in Table 1 a 300 mL sample (Sample A in Table 1) of an oil-in-water emulsion containing 115 g ai/L [80 g ae/L] of fluroxypyr MHE and 380 g ai/L [300 g ae/L] of glyphosate DMA, respectively.
  • the above oil phase containing fluroxypyr MHE was slowly added into 229 g of the glyphosate DMA salt concentrate at 7,000-11,000 rpm (depending on the desired emulsion size) by using a Silverson high-shear homogenizer. 1.8 g water was eventually added to achieve the desired concentration.
  • a stable, homogenous oil-in-water emulsion concentrate containing fluroxypyr MHE and glyphosate DMA was generated in this manner.
  • Samples C and D contain 86 g ai/L of fluroxypyr meptyl and 355 g ai/L of glyphosate DMA.
  • Sample E contains 29 g ai/L of haloxyfop-R-methyl and 380 g ai/L of glyphosate DMA.
  • the homogenous oil-in-water emulsion concentrates (Samples A, B, C, D and E) thus prepared were stable to coalescence and crystallization while stored at 54° C. for 4 weeks or while stored at 5° C. for 4 weeks.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Dentistry (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Toxicology (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

Novel high-strength herbicidal oil-in-water emulsions containing a water soluble salt of glyphosate and an oil soluble herbicide active ingredient show enhanced stability to oil phase coalescence and active ingredient crystallization by the use of specific surfactants and water immiscible organic solvents.

Description

  • This application claims the benefit of U.S. Provisional Patent Application Ser. No. 61/482,716 filed May 5, 2011.
  • BACKGROUND
  • A common method of herbicidal treatment in agricultural endeavors is to treat a field to remove or control unwanted vegetation in preparation for planting a crop plant or seed, a method otherwise known as a “burndown” herbicide treatment. However, single herbicides typically lack the weed control spectrum, e.g., the range of weed species effectively controlled by the herbicide, to fully control the diversity of weeds in such an environment and therefore, it is common to apply two or more herbicides simultaneously in order to achieve the desired spectrum of control with the burndown treatment. To facilitate this application of two or more herbicides, the herbicides are often sold separately and mixed in a spray tank by the end user. A more convenient way to deliver these herbicides is to formulate them into a single pre-mix concentrate that can easily be measured and diluted in water by the end user prior to application by spraying.
  • Glyphosate containing compositions are of particular interest in burndown herbicide applications due to their wide spectrum of weed control. These compositions are made more useful by expanding their spectrum of weed control even further by the addition of an oil soluble herbicide. An oil-in-water emulsion (EW) composition may be used to combine an oil soluble herbicide and a water soluble herbicide, such as a glyphosate, into a pre-mix herbicide concentrate where droplets of oil are stabilized by surfactant emulsifiers as a discrete phase and are uniformly dispersed in water as a continuous phase.
  • Oil-in-water emulsions can have stability issues caused by one or more factors. Interactions or reactions of an ingredient in the aqueous phase with component(s) of the dispersed oil phase include, but are not limited to, crystal formation and growth due to Ostwald ripening of an oil phase component or an aqueous phase component, or chemical degradation of ingredients in either the oil phase or the aqueous phase. These degradations may be caused by the presence of one or more components in the oil-in-water emulsion and can lead to formulation instability. Migration of water into the oil phase and contact with the active ingredient dissolved in the oil phase or migration of the active ingredient into the water phase or to the oil-water interface can lead to one or more of active ingredient hydrolysis, crystal formation or Ostwald ripening with possible formulation instability or unsuitability for agricultural spray applications.
  • It can be particularly challenging to develop stable oil-in-water emulsions containing a high ionic strength aqueous solution such as, for example, a water solution containing a soluble glyphosate salt. The high ionic strength aqueous solution can destabilize the emulsion leading to coalescence of the oil droplets into larger sized oil droplets which may ultimately cause the emulsion to separate into two liquid layers. This undesired phenomenon has been attributed to the electrolyte decreasing the electrostatic repulsive force between the dispersed droplets, thus causing the droplets to agglomerate. This stability issue becomes more severe in a high load emulsion system, and at high temperature extremes. Previous efforts to combine oil soluble herbicides with aqueous solutions containing salts of glyphosate in a liquid concentrate formulation have been disclosed, for example, in U.S. Pat. No. 6,713,433 B2, U.S. Pat. No. 6,689,719 and U.S. Pat. No. 6,369,001.
  • High-strength formulations are desirable for a variety of economic and environmental reasons. For example, it is desirable to provide a high-strength concentrate in order to reduce shipping and handling costs and to reduce the amount of packaging material that must be disposed after use of the product. The high-strength concentrates should be stable and retain potency during storage and shipping. Furthermore, the high-strength concentrate should be a homogeneous liquid emulsion that is stable at temperatures at least as high as about 50 ° C. and should not exhibit any precipitation of solids at temperatures as low as about 0 ° C.
  • SUMMARY
  • A stable high-strength herbicidal oil-in-water emulsion is disclosed that includes:
  • a) a discontinuous oil phase comprising, with respect to the oil-in-water emulsion, from about 25 grams active ingredient per liter (g ai/L) to about 300 g ai/L of at least one oil soluble herbicide active ingredient and from 0 grams per liter (g/L) to about 300 g/L of a water immiscible organic solvent;
  • b) a continuous aqueous phase comprising, with respect to the oil-in-water emulsion, from about 260 g ai/L to about 570 g ai/L of a water soluble salt of glyphosate and from about 200 g/L to about 500 g/L of water; and
  • c) at least two non-ionic EO/PO block copolymer emulsifying surfactants with at least one having a hydrophile lipophile balance (HLB) value of about 13 to about 16 and at least one having an HLB value of about 22 to about 29 and each having a molecular weight (mw) of about 5000 or higher, with the combined emulsifying surfactants comprising, with respect to the oil-in-water emulsion, from about 1 g/L to about 200 g/L.
  • Additionally, a method of preparing a stable high-strength herbicidal oil-in-water emulsion composition is disclosed that includes:
  • a) preparing a discontinuous oil phase comprising, with respect to the oil-in-water emulsion, from about 25 grams active ingredient per liter (g ai/L) to about 300 g ai/L of at least one oil soluble herbicide active ingredient and from 0 grams per liter (g/L) to about 300 g/L of a water immiscible organic solvent;
  • b) preparing a continuous aqueous phase comprising, with respect to the oil-in-water emulsion, from about 260 g ai/L to about 570 g ai /L of a water soluble salt of glyphosate and from about 200 g/L to about 500 g/L of water, and at least two non-ionic EO/PO block copolymer emulsifying surfactants with at least one having a hydrophile lipophile balance (HLB) value of about 13 to about 16 and at least one having an HLB value of about 22 to about 29 and with each having a molecular weight (mw) of about 5000 or higher, with the combined emulsifying surfactants comprising, with respect to the oil-in-water emulsion, from about 1 g/L to about 200 g/L; and
  • c) adding the oil phase into the aqueous phase under high shear homogenization until an emulsion is achieved.
  • DETAILED DESCRIPTION
  • A high-strength, herbicidal oil-in-water emulsion pre-mix composition comprising a dispersed oil phase containing at least one oil soluble herbicide and a water immiscible organic solvent, a continuous aqueous phase containing a water soluble salt of glyphosate, and at least two non-ionic EO/PO block copolymer emulsifying surfactant, one having an hydrophile lipophile balance (HLB) value of about 13 to about 16 and the other having an HLB value of about 22 to about 29, both having a molecular weight (mw) of about 5000 or higher is disclosed. The composition may optionally include additional active ingredients and inert formulation ingredients.
  • The oil soluble herbicide active ingredient contained in the discontinuous oil phase of the compositions disclosed herein may generally be selected from the class of synthetic auxin and lipid synthesis inhibitor (ACCase inhibitors) herbicides. Preferred herbicide active ingredients include, but are not limited to, oil soluble derivatives of carboxylic acid herbicides, such as esters of the following: benzoic acid herbicides, such as dicamba; phenoxyalkanoic acid herbicides, such as 2,4-D, MCPA and 2,4-DB; pyridinecarboxylic acid herbicides, such as aminopyralid, picloram and clopyralid; pyridinyloxyalkanoic acid herbicides such as fluroxypyr and triclopyr; pyrimidinecarboxylic acids, such as aminocyclopyrachlor; and, esters of the aryloxyphenoxypropionic acids, such as cyhalofop, clodinafop, diclofop, fenoxaprop, fluazifop-P, haloxyfop, haloxyfop-R, metamifop, propaquizafop and quizalofop-P. Preferred oil-soluble herbicide active ingredients also include cyclohexanediones, such as cycloxydim, sethoxydim, tralkoxydim and the like. The oil soluble herbicide active ingredient of the compositions disclosed herein generally has a water solubility of less than about 3000 parts per million (ppm) and preferably less than about 1000 ppm. The oil soluble herbicide active ingredient comprises, with respect to the oil-in-water emulsion, from about 25 g ai/L to about 300 g ai/L.
  • The water immiscible organic solvent of the compositions disclosed herein generally has a water solubility of less than about 1000 ppm and may include, but is not limited to, one or more of petroleum fractions or hydrocarbons such as mineral oil, kerosene, paraffinic oils, mixed naphthalene and alkyl naphthalene fractions, aromatic solvents, particularly alkyl substituted benzenes such as xylene or propylbenzene fractions, and the like; heavy aromatic solvent naphtha such as Aromatic 150 fluid (Exxon Mobil Chemical; Houston, Tex.), dialkyl amides of carboxylic acids, particularly the dimethyl amides of fatty acids such as the dimethyl amide of caprylic acid and the like; vegetable, animal, algae or seed oils such as soybean oil, rape seed oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cotton seed oil, linseed oil, palm oil, peanut oil, safflower oil, sesame oil, tung oil and the like; esters of the above vegetable, animal, algae or seed oils; chlorinated aliphatic and aromatic hydrocarbons such as 1,1,1-trichloroethane and chlorobenzene; ketones such as isophorone and trimethylcyclohexanone (dihydroisophorone); and acetate esters of C4-C10 alcohols such as hexyl, or heptyl acetate, and the like. In some instances, where the herbicide active ingredient is a liquid under normal operating conditions, the oil phase may contain very little or none of the water immiscible organic solvent.
  • Preferred water immiscible organic solvents include one or more of petroleum fractions or hydrocarbons such as mineral oil, paraffinic oils and aromatic solvents like xylene, propylbenzene fractions, alkyl naphthalene fractions, and the like; dialkyl amides of carboxylic acids, particularly the dimethyl amides of fatty acids such as the dimethyl amide of caprylic acid and the like; vegetable or seed oils such as soybean oil, rape seed oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cotton seed oil, linseed oil, palm oil, peanut oil, safflower oil, sesame oil, tung oil and the like; and C1-C5 esters of vegetable or seed oils and the like. The water immiscible organic solvent may comprise, with respect to the oil-in-water emulsion, from about 0 g/L to about 300 g/L, preferably from about 10 g/L to about 300 g/L.
  • Optional ingredients that may be added to the discontinuous oil phase described herein include emulsion stabilizers such as, but not limited to, one or more low molecular weight homopolymers (<5000 mw) of the following: polyolefins, such as polybutadiene, polyisoprene, poly(substituted butadienes), such as poly(2-t-butyl-1,3-butadiene), polyethylene, chlorinated polyethylene, polypropylene, polybutene, polyisobutene, polycyclopentylethylene and polycyclolhexylethylene; polyacrylates, including polyalkylacrylates and polyarylacrylates; polymethacrylates, including polyalkylmethacrylates and polyarylmethacrylates; polydisubstituted esters, such as poly(di-n-butylitaconate) and poly(amylfumarate); polyvinylethers, such as poly(butoxyethylene) and poly(benzyloxyethylene); poly(methyl isopropenyl ketone); polyvinyl chloride; polyvinyl carboxylate esters such as polyvinyl acetate, polyvinyl propionate, polyvinyl butyrate, polyvinyl caprylate, polyvinyl laurate, polyvinyl stearate and polyvinyl benzoate; polystyrenes, like polystyrene, poly-t-butyl styrene, poly (substituted styrene) and poly(biphenyl ethylene); polycyclodienes, like poly(1,3-cyclohexadiene) and polycyclopentadiene and the like; and low molecular weight (<5000 mw) co-polymers of styrene, alkyl styrenes, isoprene, butenes, isobutenes, of which Indopol® H-15 is a preferred example (Indopol is trademark of INEOS Oligomers), butadiene, acrylonitrile, alkyl acrylates, alkyl methacrylates, vinyl chloride, vinylidene chloride, vinyl esters of lower carboxylic acids and alpha, beta-ethylenically unsaturated carboxylic acids and esters thereof, including co-polymers containing three or more different monomer species, and the like. Additional emulsion stabilizers include paraffinic hydrocarbons such as tetradecane, hexadecane and the like.
  • The continuous aqueous phase of the compositions disclosed herein comprises water as the solvent medium and a water soluble salt of glyphosate. Typically, water in the aqueous phase of the emulsion formulation is used to dissolve the salt of glyphosate and any other water soluble ingredients and to balance the final composition. The continuous aqueous phase of the compositions disclosed herein may comprise, with respect to the oil-in-water emulsion, from about 200 g/L to about 500 g/L, preferably from about 200 g/L to about 400 g/L of water.
  • The water soluble salt of glyphosate contained in the continuous aqueous phase of the compositions disclosed herein may comprise one or more of an organo ammonium salt and the potassium salt of glyphosate. Suitable water soluble organo ammonium salts of glyphosate include, but are not limited to, dimethyl ammonium, isopropyl ammonium, monoethanol ammonium and the N,N,N,N-trimethylethanol ammonium (choline) salt of glyphosate. The water soluble salt of glyphosate may comprise, with respect to the oil-in-water emulsion, from about 260 g ai/L to about 570 g ai/L, preferably from about 260 g ai/L to about 450 g ai/L.
  • The compositions described herein also include at least two non-ionic EO/PO block copolymer emulsifying surfactants with a hydrophile lipophile balance (HLB) value of 13 or higher and a molecular weight (mw) of about 5000 or higher. The utility of non-ionic surfactants in emulsifying an oil-water mixture may in part be predicted by the Hydrophile-Lipophile Balance (HLB) values of the surfactants. The HLB value of a surfactant estimates the balance between the oil soluble and water soluble moieties in a surface active molecule (i.e., a surfactant). A more oil-soluble emulsifier will have a lower HLB value (less than about 7) and a more water-soluble emulsifier will have a larger HLB value (greater than about 7). The HLB approach is a useful method to select an emulsifier for a particular application and is more fully described in “The HLB System” an online publication available from the crodalubricants.com website at the following link:
    • www.crodalubricants.com/download.aspx?s=133&m=doc&id=267 .
  • The non-ionic EO/PO block copolymer emulsifying surfactants of the compositions disclosed herein include at least one surfactant with an HLB value of about 13 to about 16 and at least one surfactant with an HLB value of about 22 to about 29, with the surfactants having a molecular weight of a least about 5000. The EO/PO block copolymer emulsifying surfactants described herein include both di- and tri-block co-polymers of ethylene oxide (EO) and propylene oxide (PO). Preferred non-ionic EO/PO block copolymer surfactants of the compositions disclosed herein include, but are not limited to, Pluronic® L35, L44, L64, P65, P75, P84, P85, P104, P105, F77, F87, F88, F68, F68 LF, F98, F108, F127, 17R8 and 25R8; Tetronic® 704, 707, 904, 1104, 1107, 1307, 1504, 1508, 50R8 and 90R8; Macol® 15-20; Toximul® 8323 and 8323/33; Step-Flow® 26, 26F and 1500; Synperonic® PE 30/40, PE 30/80 and PE 39/70; Pegol® 10R8, 17R8, 25R8, F-68LF, F-108, F-127, L-10, L-35, L-44, P-65, P-75 and P-85; Antarox® 724/P, T-Det® BP-1, EPO-64 and EPO-104; Agrilan® AEC167; Monolan® 4500, 6400, 8000 E/80 and 12,000 E/80; Genapol® PF80 Powder; Hartopol® P85; Surfonic® POA-L44 and L64; Soprophor® 796P, BSU, CY8, S25 and S25/80; and Atlas® G-5000. (Pluronic, Tetronic and Macol are trademarks of BASF Aktiengesellschaft; Toximul and Step-Flow are trademarks of Stepan; Synperonic and Pegol are trademarks of Croda; Antarox and Soprophor are trademarks of Rhodia Inc., T-Det is a trademark of Harcos; Agrilan and Monolan are trademarks of Akzo Nobel; Genapol is a trademark of Clariant; Hartopol and Surfonic are trademarks of Huntsman; Atlas is a trademark of Uniqema). The non-ionic EO/PO block copolymer emulsifying surfactants of the compositions disclosed herein may comprise, with respect to the oil-in-water emulsion, from about 1 g/L to about 200 g/L, preferably from about 1 g/L to about 100 g/L.
  • The compositions described herein may optionally contain additional water soluble herbicide active ingredients if they cause no incompatibility or active ingredient stability issues to other ingredients of the composition. These water soluble herbicide active ingredients may be selected from, but are not limited to, alkali metal salts or amine salts of benzoic acids, phenoxyalkanoic acids, pyridinecarboxylic acids, pyrimidinecarboxylic acids and pyridinyloxycarboxylic acids such as, dicamba, 2,4-D, MCPA, 2,4-DB, aminopyralid, aminocyclopyrachlor, picloram, clopyralid, fluroxypyr and triclopyr, and alkali metal salts of bromoxynil and ioxynil. The amines are comprised of primary, secondary or tertiary alkylamines, alkanolamines, alkylalkanolamines or alkoxyalkanolamines wherein the alkyl and alkanol groups are saturated and contain C1-C4 alkyl groups individually. The alkali metals are comprised of sodium and potassium.
  • The compositions described herein may optionally contain inert formulation ingredients such as, but not limited to, adjuvants, antifoam agents, dispersants, surfactants, spray drift reduction agents, stabilizers and wetting agents. These optional inert ingredients may include surfactants conventionally used in the art of formulation that are described, inter alia, in “McCutcheon's Detergents and Emulsifiers Annual,” MC Publishing Corp., Ridgewood, N.J., 1998 and in the “Encyclopedia of Surfactants,” Vol. I-III, Chemical Publishing Co., N.Y., 1980-81. Adjuvants that are particularly well-suited for use in the compositions disclosed herein may include one or more of: alkylamine surfactants having 8 to 22 carbon atoms such as Armeen® DMTD and Duomeen® TTM; alkoxylated alkylamine surfactants having 8 to 22 carbon atoms and a total of 1-20 alkylene oxide groups such as Ethomeen® C/12, Ethomeen® T/12, Ethoduomeen® T/13 and Propomeen® T/12; etheramine surfactants such as Tomah® E-14-2, Tomah® E-14-5 and Tomah® PA-17; amine oxide surfactants such as Aromox C/12, Aromox DMC, Ammonyx® LO, Ammonyx® CDO and Tomah®AO-14-2; amidoamine surfactants such as Adsee C80W; quaternary ammonium surfactants such as Arquad® T/50, Arquad° APA-E, Duoquad° T/50, Ethoquad® C/12, Ethoquad® 18/12 and Tomah® Q-14-2; amphoteric surfactants such as Dehyton® AB-30, Geronol® CF/AS 30, Tego® Betaine F 50t and Miranol® C2M-SF (Disodium Cocoampho Dipropionate); alcohol ethoxylates such as Tergitol® 15S20; alcohol ethoxylate phosphate esters such as Geranol® CF/AR; alkyl polyglycosides such as Akzo Nobel's AG 6202 and AG 6210, and Cognis' Agnique PG 8107-U (C8-16 alkyl polyglucoside in which the alkyl group contains 8 to 10 carbon atoms and having an average degree of polymerization of 1.7); and ester derivatives of alkyl polyglycosides such as the Eucarol® AGE surfactants. (Armeen, Duomeen, Ethomeen, Ethoduomeen, Propomeen, Aromox, Arquad, Duoquad, Ethoquad and Adsee are trademarks of Akzo Nobel; Tomah is a trademark of Air Products; Ammonyx is a trademark of Stepan; Dehyton and Agnique are a trademarks of Cognis; Geronol and Miranol are trademarks of Rhodia Inc.; Tego is a trademark of Goldschmidt; Tergitol is a trademark of The Dow Chemical Company; Eucarol is a trademark of Lamberti)
  • The compositions disclosed herein provide a high-strength herbicidal oil-in-water emulsion composition that is storage stable at high temperatures. That is, the composition forms a stable, homogeneous emulsion that does not exhibit coalescence under the storage conditions. More preferably, the composition described herein is stable at temperatures of greater than or equal to about 40° C. for a period of at least 4 weeks, more preferably, at temperatures greater than or equal to about 54° C. for a period of at least about 4 weeks.
  • Furthermore, the high-strength oil-in-water emulsion composition described herein also does not exhibit separation or precipitation (or crystallization) of any of the components at low temperatures. For example, the composition remains a homogeneous emulsion at temperatures below about 20° C., more preferably at temperatures below about 10° C. and most preferably at a temperature equal to or less than about 5° C. for a period of at least about 4 weeks.
  • In a typical procedure for preparing the high-strength oil-in-water emulsion compositions described herein, the aqueous phase is prepared by mixing the water with water soluble or water dispersible ingredients including, but not limited to, water soluble or water dispersible dispersing or emulsifying surfactants, water soluble active ingredients and optionally, other inert ingredients such as thickeners, pH buffers, wetting agents, antifreeze agents, antifoam agents, biocides, etc. The oil phase is prepared by mixing the oil-soluble emulsifying surfactants with oil miscible or soluble ingredients, including but not limited to, water immiscible organic solvents and oil soluble active ingredients. The final emulsion formulation is prepared by slowly adding the oil phase into the aqueous phase under high shear homogenization until a desired emulsion droplet size is achieved. Emulsion droplet sizes can be, for example, between 0.1μm and 5 μm, between 0.1 μm and 4 μm, 0.1 μm and 3 μm, 0.1 μm and 2 μm, or 0.1 μm and 1 μm.
  • An example of a stable, high-strength oil-in-water emulsion composition described herein in which coalescence of the dispersed oil phase and crystallization and Oswald ripening of an oil soluble active ingredient is retarded comprises:
  • a) a discontinuous oil phase comprising, with respect to the oil-in-water emulsion, from about 25 g ai/L to about 300 g ai/L of fluroxypyr-meptyl and from about 1 g/L to about 300 g/L of naphthalene depleted Aromatic 150 fluid;
  • b) a continuous aqueous phase comprising, with respect to the oil-in-water emulsion, from about 310 g ai/L to about 570 g ai/L of glyphosate dimethyl ammonium and from about 200 g/L to about 500 g/L of water;
  • c) two non-ionic EO/PO block copolymer emulsifying surfactants with at least one having a hydrophile lipophile balance (HLB) value of about 13 to about 16 and at least one having an HLB value of about 22 to about 29 and with each surfactant having a molecular weight (mw) of about 5000 or higher together comprising, with respect to the oil-in-water emulsion, from about 1 g/L to about 200 g/L each of Pluronic® F68 LF and Soprophor® 796/P; and
  • d) optionally, other inert formulation ingredients.
  • In addition to the compositions and uses set forth above, also described herein are compositions and use of oil-in-water emulsions in combination with one or more additional compatible ingredients. Other additional ingredients may include, for example, one or more other pesticides, dyes, and any other additional ingredients providing functional utility, such as, for example, stabilizers, compatibility agents, fragrants, viscosity-modifying additives, suspension aids, dispersants, and freeze-point depressants.
  • The aqueous herbicidal compositions described herein may optionally be diluted in an aqueous spray mixture for agricultural application such as for burndown weed control in crop fields prior to planting. Such compositions are typically diluted with an inert carrier, such as water, before application. The diluted compositions, which are usually applied to weeds, the locus of weeds or the locus of where weeds may eventually emerge, generally contain about 0.0001 to about 1 weight percent active ingredient and preferably contain about 0.001 to about 0.05 weight percent active ingredient. The compositions disclosed herein can be applied to weeds or their locus by the use of conventional ground or aerial sprayers, by addition to irrigation water and by other conventional means known to those skilled in the art.
  • The herbicidal compositions described herein may be applied in conjunction with one or more other herbicides to control a wider variety of undesirable vegetation. When used in conjunction with other herbicides, the presently claimed compositions can be formulated with the other herbicide or herbicides as premix concentrates, tank mixed with the other herbicide or herbicides for spray application or applied sequentially with the other herbicide or herbicides in separate spray applications.
  • The following Examples are presented to illustrate various aspects of the compositions and methods described herein and should not be construed as limitations to the claims.
  • Example 1 Preparation of a Stable Oil-in-Water Emulsion Containing Glyphosate Dimethyl Ammonium (DMA) and Fluroxypyr Meptyl (MHE)
  • A glyphosate DMA salt concentrate was prepared by mixing 247.4 g glyphosate acid technical (purity 97%) with 1.1 molar equivalents of dimethylamine aqueous solution (40% in water) to form a homogeneous clear solution at ambient temperature. To the glyphosate DMA solution were then added 31.2 g of Agnique® PG 8107-U (Agnique is a registered trademark of Cognis) and 154.9 g of water to achieve a concentration of 608 g ai/L [480 grams acid equivalent per liter (g ae/L)] of glyphosate DMA. An oil phase was prepared by dissolving 35.6 g of fluroxypyr MHE (purity 97.1%) in 53.4 g of Aromatic 150 ND fluid (ExxonMobil Chemical Company; Houston, Tex.) containing 13.7 g of Pluronic® F68 LF
  • (Pluronic is a registered trademark of BASF Aktiengesellschaft), 5.1 g of Soprophor® 796/P (Soprophor is a registered trademark of Rhodia Inc) and 3.4 g of Indopol® H15 (Indopol is a registered trademark of INEOS Oligomers) to provide a solution while maintaining the temperature at 50 ° C. Finally, to prepare a 300 mL sample (Sample A in Table 1) of an oil-in-water emulsion containing 115 g ai/L [80 g ae/L] of fluroxypyr MHE and 380 g ai/L [300 g ae/L] of glyphosate DMA, respectively, the above oil phase containing fluroxypyr MHE was slowly added into 229 g of the glyphosate DMA salt concentrate at 7,000-11,000 rpm (depending on the desired emulsion size) by using a Silverson high-shear homogenizer. 1.8 g water was eventually added to achieve the desired concentration. A stable, homogenous oil-in-water emulsion concentrate containing fluroxypyr MHE and glyphosate DMA was generated in this manner.
  • TABLE 1
    Oil-in-Water Emulsion Concentrates (ingredients in weight percent)
    Sample Sample Sample Sample Sample
    Component A1 B1 C2 D2 E3
    Fluroxypyr-meptyl 10.1 10.1 7.7 7.7 /
    Haloxyfop-R-methyl / / / / 2.4
    Glyphosate DMA 33.3 33.3 31.4 31.4 33.3
    Agnique ® PG 8107-U 5.5 5.5 5.2 5.2 5.5
    Pluronic ® F-68 LF 4.0 / 4.0 / 7.2
    Pluronic ® P-104 / 3.9 / 4.0 /
    Soprophor ® 796P 1.5 1.0 1.5 1.0 1.8
    Aromatic 150 ND 15.8 16.1 16.7 18.3 14.8
    Indopol ® H-15 1.0 / 1.0 / /
    water 28.8 30.1 32.5 32.4 35.0
    1Samples A and B contain 115 grams active ingredient per liter (g ai/L) of fluroxypyr meptyl and 380 g ai/L of glyphosate dimethyl ammonium (DMA).
    2Samples C and D contain 86 g ai/L of fluroxypyr meptyl and 355 g ai/L of glyphosate DMA.
    3Sample E contains 29 g ai/L of haloxyfop-R-methyl and 380 g ai/L of glyphosate DMA.
  • The homogenous oil-in-water emulsion concentrates (Samples A, B, C, D and E) thus prepared were stable to coalescence and crystallization while stored at 54° C. for 4 weeks or while stored at 5° C. for 4 weeks.
  • The present invention is not limited in scope by the embodiments disclosed herein which are intended as illustrations of a few aspects of the invention and any embodiments which are functionally equivalent are within the scope of this invention. Various modifications of the compositions and methods in addition to those shown and described herein will become apparent to those skilled in the art and are intended to fall within the scope of the appended claims. Further, while only certain representative combinations of the composition components and method steps disclosed herein are specifically discussed in the embodiments above, other combinations of the composition components and method steps will become apparent to those skilled in the art and also are intended to fall within the scope of the appended claims. Thus a combination of components or method steps may be explicitly mentioned herein; however, other combinations of components and method steps are included, even though not explicitly stated. The term “comprising” and variations thereof as used herein is used synonymously with the term “including” and variations thereof and are open, non-limiting terms.

Claims (20)

1. A stable high-strength herbicidal oil-in-water emulsion composition comprising:
a) a discontinuous oil phase comprising, with respect to the oil-in-water emulsion, from about 25 grams active ingredient per liter (g ai/L) to about 300 g ai/L of at least one oil soluble herbicide active ingredient and from 0 grams per liter (g/L) to about 300 g/L of a water immiscible organic solvent;
b) a continuous aqueous phase comprising, with respect to the oil-in-water emulsion, from about 260 g ai/L to about 570 g ai /L of a water soluble salt of glyphosate and from about 200 g/L to about 500 g/L of water; and
c) at least two non-ionic EO/PO block copolymer emulsifying surfactants with at least one having a hydrophile lipophile balance (HLB) value of about 13 to about 16 and at least one having an HLB value of about 22 to about 29 and with each having a molecular weight (mw) of about 5000 or higher, with the combined emulsifying surfactants comprising, with respect to the oil-in-water emulsion, from about 1 g/L to about 200 g/L.
2. The composition of claim 1, wherein the at least one oil soluble herbicide active ingredients is a synthetic auxin or a lipid synthesis inhibitor herbicide.
3. The composition of claim 1, wherein the at least one oil soluble herbicide active ingredient has a water solubility of less than about 3000 parts per million (ppm).
4. The composition of claim 1, wherein the water immiscible organic solvent has a water solubility of less than about 1000 ppm.
5. The composition of claim 1, wherein the discontinuous oil phase includes from 0 grams per liter (g/L) to about 300 g/L of a water immiscible organic solvent.
6. The composition of claim 1, wherein the discontinuous oil phase further includes an emulsion stabilizer.
7. The composition of claim 1, wherein the continuous oil phase includes from about 200 g/L to about 400 g/L of water.
8. The composition of claim 1, wherein the continuous oil phase includes a water soluble salt of glyphosate.
9. The composition of claim 8, wherein the water soluble salt of glyphosate is an organo ammonium salt or a potassium salt.
10. The composition of claim 8, wherein the organo ammonium salt is a dimethyl ammonium, a isopropyl ammonium, a monoethanol ammonium, or a N,N,N,N-trimethylethanol ammonium (choline) salt.
11. The composition of claim 8, wherein the continuous aqueous phase includes about 260 g ai/L to about 450 g ai/L of the water soluble salt of glyphosate.
12. The composition of claim 1, wherein the at least two non-ionic EO/PO block copolymer emulsifying surfactants include both di- and tri-block co-polymers of ethylene oxide (E0) and propylene oxide (PO).
13. The composition of claim 1, wherein the combined emulsifying surfactants comprise, with respect to the oil-in-water emulsion, about 1 g/L to about 100 g/L.
14. The composition of claim 1, further including additional water soluble herbicide active ingredients.
15. The composition of claim 1, wherein the composition forms a stable, homogeneous emulsion that does not exhibit coalescence under the storage conditions.
16. The composition of claim 1, wherein the composition is stable at temperatures of greater than or equal to about 40° C. for a period of at least 4 weeks.
17. The composition of claim 1, wherein the composition does not exhibit separation or precipitation (or crystallization) of any of the components at temperatures below about 20° C.
18. The composition of claim 1, wherein the discontinuous oil phase comprises fluroxypyr-meptyl and naphthalene depleted Aromatic 150 fluid, and the continuous aqueous phase comprises glyphosate dimethyl ammonium and water.
19. A method of preparing a stable high-strength herbicidal oil-in-water emulsion composition comprising:
a) preparing a discontinuous oil phase comprising, with respect to the oil-in-water emulsion, from about 25 grams active ingredient per liter (g ai/L) to about 300 g ai/L of at least one oil soluble herbicide active ingredient and from 0 grams per liter (g/L) to about 300 g/L of a water immiscible organic solvent;
b) preparing a continuous aqueous phase comprising, with respect to the oil-in-water emulsion, from about 260 g ai/L to about 570 g ai /L of a water soluble salt of glyphosate and from about 200 g/L to about 500 g/L of water, and at least two non-ionic EO/PO block copolymer emulsifying surfactants with at least one having a hydrophile lipophile balance (HLB) value of about 13 to about 16 and at least one having an HLB value of about 22 to about 29 and with each having a molecular weight (mw) of about 5000 or higher, with the combined emulsifying surfactants comprising, with respect to the oil-in-water emulsion, from about 1 g/L to about 200 g/L; and
c) adding the oil phase into the aqueous phase under high shear homogenization until an emulsion is achieved.
20. The method of preparing the stable high-strength herbicidal oil-in-water emulsion composition of claim 19, wherein the emulsion droplet size is between 0.1 μm and 5 μm.
US13/463,848 2011-05-05 2012-05-04 Stable high strength oil-in-water emulsions Abandoned US20120283098A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US13/463,848 US20120283098A1 (en) 2011-05-05 2012-05-04 Stable high strength oil-in-water emulsions
US14/510,289 US11058108B2 (en) 2011-05-05 2014-10-09 Stable high strength oil-in-water emulsions

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161482716P 2011-05-05 2011-05-05
US13/463,848 US20120283098A1 (en) 2011-05-05 2012-05-04 Stable high strength oil-in-water emulsions

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US14/510,289 Continuation US11058108B2 (en) 2011-05-05 2014-10-09 Stable high strength oil-in-water emulsions

Publications (1)

Publication Number Publication Date
US20120283098A1 true US20120283098A1 (en) 2012-11-08

Family

ID=47090620

Family Applications (2)

Application Number Title Priority Date Filing Date
US13/463,848 Abandoned US20120283098A1 (en) 2011-05-05 2012-05-04 Stable high strength oil-in-water emulsions
US14/510,289 Active US11058108B2 (en) 2011-05-05 2014-10-09 Stable high strength oil-in-water emulsions

Family Applications After (1)

Application Number Title Priority Date Filing Date
US14/510,289 Active US11058108B2 (en) 2011-05-05 2014-10-09 Stable high strength oil-in-water emulsions

Country Status (19)

Country Link
US (2) US20120283098A1 (en)
EP (1) EP2704561B1 (en)
CN (1) CN103648274B (en)
AR (1) AR086284A1 (en)
AU (1) AU2012250601B2 (en)
BR (1) BR102012010651B8 (en)
CA (1) CA2834789C (en)
CL (1) CL2013003129A1 (en)
CO (1) CO6801801A2 (en)
ES (1) ES2592529T3 (en)
IL (1) IL229174A (en)
MA (1) MA35164B1 (en)
MX (1) MX2013012893A (en)
PL (1) PL2704561T3 (en)
RU (1) RU2013153904A (en)
TN (1) TN2013000457A1 (en)
TW (1) TW201247099A (en)
WO (1) WO2012151455A1 (en)
ZA (1) ZA201308084B (en)

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013096443A1 (en) * 2011-12-20 2013-06-27 Dow Agrosciences Llc Synergistic herbicidal composition containing fluroxypyr and glyphosate
US9421758B2 (en) 2014-09-30 2016-08-23 Xerox Corporation Compositions and use of compositions in printing processes
US9428663B2 (en) 2014-05-28 2016-08-30 Xerox Corporation Indirect printing apparatus employing sacrificial coating on intermediate transfer member
US9494884B2 (en) 2014-03-28 2016-11-15 Xerox Corporation Imaging plate coating composite composed of fluoroelastomer and aminosilane crosslinkers
US9550908B2 (en) 2014-09-23 2017-01-24 Xerox Corporation Sacrificial coating for intermediate transfer member of an indirect printing apparatus
US9593255B2 (en) 2014-09-23 2017-03-14 Xerox Corporation Sacrificial coating for intermediate transfer member of an indirect printing apparatus
US9611404B2 (en) * 2014-09-23 2017-04-04 Xerox Corporation Method of making sacrificial coating for an intermediate transfer member of indirect printing apparatus
US9683130B2 (en) 2014-03-19 2017-06-20 Xerox Corporation Polydiphenylsiloxane coating formulation and method for forming a coating
US9718964B2 (en) 2015-08-19 2017-08-01 Xerox Corporation Sacrificial coating and indirect printing apparatus employing sacrificial coating on intermediate transfer member
US9752042B2 (en) 2015-02-12 2017-09-05 Xerox Corporation Sacrificial coating compositions comprising polyvinyl alcohol and waxy starch
US9816000B2 (en) 2015-03-23 2017-11-14 Xerox Corporation Sacrificial coating and indirect printing apparatus employing sacrificial coating on intermediate transfer member
US9956760B2 (en) 2014-12-19 2018-05-01 Xerox Corporation Multilayer imaging blanket coating
WO2018082895A1 (en) * 2016-11-02 2018-05-11 Syngenta Participations Ag Agrochemical concentrates containing alkyl polyglucoside and non-ionic surfactant
WO2019236723A1 (en) * 2018-06-05 2019-12-12 Monsanto Technology Llc Herbicidal compositions
WO2021140442A1 (en) * 2020-01-10 2021-07-15 UPL Corporation Limited A stable agrochemical composition and process for preparation thereof
US11478991B2 (en) 2020-06-17 2022-10-25 Xerox Corporation System and method for determining a temperature of an object
US11498354B2 (en) 2020-08-26 2022-11-15 Xerox Corporation Multi-layer imaging blanket
US11499873B2 (en) 2020-06-17 2022-11-15 Xerox Corporation System and method for determining a temperature differential between portions of an object printed by a 3D printer
US11767447B2 (en) 2021-01-19 2023-09-26 Xerox Corporation Topcoat composition of imaging blanket with improved properties

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112014022126A2 (en) * 2012-03-08 2017-06-20 Dow Agrosciences Llc AQUEOUS CONCENTRATE COMPOSITIONS, METHOD FOR REDUCING DRIFT DURING THE APPLICATION OF A PESTICIDE MIXTURE FOR AQUEOUS SPRAYING, AND METHOD FOR PREPARING SUCH MIXTURE
CN104277071B (en) * 2013-12-30 2017-03-08 山东潍坊润丰化工股份有限公司 A kind of glyphosate choline raw drug, preparation and preparation method thereof
CN113615696A (en) 2014-12-30 2021-11-09 美国陶氏益农公司 Pyridine amide compounds having fungicidal activity
CN105949237B (en) * 2016-07-14 2019-01-04 山东润博生物科技有限公司 A kind of preparation method of glyphosate dimethylamine salt raw medicine
CN106387835A (en) * 2016-08-31 2017-02-15 恒枫食品科技有限公司 Preparation method of emulsifying essence

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2267825A (en) * 1992-05-26 1993-12-22 Dowelanco Herbicide microemulsion concentrate
US6713433B2 (en) * 1999-08-11 2004-03-30 Monsanto Technology, Llc Coformulation of an oil-soluble herbicide and a water-soluble herbicide

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4440562A (en) * 1981-07-20 1984-04-03 Monsanto Company Herbicidal emulsions
US4822405A (en) * 1987-01-27 1989-04-18 American Cyanamid Company Herbicidal oil in water combination compositions of imidazolinone herbicides
US6369001B1 (en) 1999-08-11 2002-04-09 Monsanto Technology, Llc Microemulsion coformulation of a graminicide and a water-soluble herbicide
US6689716B2 (en) 2000-10-17 2004-02-10 Altair Nanomaterials Inc. Method for producing catalyst structures
ATE373422T1 (en) * 2001-09-26 2007-10-15 Platte Chemical Co MICRO-EMULSION-FORMING HERBICIDE CONCENTRATES, MICRO-EMULSIONS AND METHODS
DE102004025220A1 (en) * 2004-05-22 2005-12-08 Bayer Cropscience Gmbh Oil suspension concentrate
GB0624760D0 (en) * 2006-12-12 2007-01-17 Syngenta Ltd Herbicidal compounds
CN101406202A (en) * 2008-11-24 2009-04-15 段传进 Compound herbicide and herbicidal composition
EP2470017B1 (en) * 2009-08-27 2013-12-11 Basf Se Aqueous concentrate formulations containing saflufenacil and glyphosate
UA109416C2 (en) * 2009-10-06 2015-08-25 STABLE EMULSIONS OF OIL-IN-WATER TYPE

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2267825A (en) * 1992-05-26 1993-12-22 Dowelanco Herbicide microemulsion concentrate
US6713433B2 (en) * 1999-08-11 2004-03-30 Monsanto Technology, Llc Coformulation of an oil-soluble herbicide and a water-soluble herbicide

Cited By (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2793572A4 (en) * 2011-12-20 2015-07-15 Dow Agrosciences Llc Synergistic herbicidal composition containing fluroxypyr and glyphosate
WO2013096443A1 (en) * 2011-12-20 2013-06-27 Dow Agrosciences Llc Synergistic herbicidal composition containing fluroxypyr and glyphosate
US9683130B2 (en) 2014-03-19 2017-06-20 Xerox Corporation Polydiphenylsiloxane coating formulation and method for forming a coating
US10081739B2 (en) 2014-03-19 2018-09-25 Xerox Corporation Polydiphenylsiloxane coating formulation and method for forming a coating
US9494884B2 (en) 2014-03-28 2016-11-15 Xerox Corporation Imaging plate coating composite composed of fluoroelastomer and aminosilane crosslinkers
US9796192B2 (en) 2014-03-28 2017-10-24 Xerox Corporation Imaging plate coating composite composed of fluoroelastomer and aminosilane crosslinkers
US9428663B2 (en) 2014-05-28 2016-08-30 Xerox Corporation Indirect printing apparatus employing sacrificial coating on intermediate transfer member
US9790373B2 (en) 2014-05-28 2017-10-17 Xerox Corporation Indirect printing apparatus employing sacrificial coating on intermediate transfer member
US10336910B2 (en) 2014-09-23 2019-07-02 Xerox Corporation Sacrificial coating for intermediate transfer member of an indirect printing apparatus
US20170145240A1 (en) * 2014-09-23 2017-05-25 Xerox Corporation Method of making sacrificial coating for an intermediate transfer member of indirect printing apparatus
US9783697B2 (en) 2014-09-23 2017-10-10 Xerox Corporation Sacrificial coating for intermediate transfer member of an indirect printing apparatus
US9611404B2 (en) * 2014-09-23 2017-04-04 Xerox Corporation Method of making sacrificial coating for an intermediate transfer member of indirect printing apparatus
US9593255B2 (en) 2014-09-23 2017-03-14 Xerox Corporation Sacrificial coating for intermediate transfer member of an indirect printing apparatus
US9926456B2 (en) * 2014-09-23 2018-03-27 Xerox Corporation Method of making sacrificial coating for an intermediate transfer member of indirect printing apparatus
US9550908B2 (en) 2014-09-23 2017-01-24 Xerox Corporation Sacrificial coating for intermediate transfer member of an indirect printing apparatus
US10675862B2 (en) 2014-09-30 2020-06-09 Xerox Corporation Compositions and use of compositions in printing processes
US10280313B2 (en) 2014-09-30 2019-05-07 Xerox Corporation Compositions and use of compositions in printing processes
US9421758B2 (en) 2014-09-30 2016-08-23 Xerox Corporation Compositions and use of compositions in printing processes
US9956760B2 (en) 2014-12-19 2018-05-01 Xerox Corporation Multilayer imaging blanket coating
US9752042B2 (en) 2015-02-12 2017-09-05 Xerox Corporation Sacrificial coating compositions comprising polyvinyl alcohol and waxy starch
US9816000B2 (en) 2015-03-23 2017-11-14 Xerox Corporation Sacrificial coating and indirect printing apparatus employing sacrificial coating on intermediate transfer member
US9718964B2 (en) 2015-08-19 2017-08-01 Xerox Corporation Sacrificial coating and indirect printing apparatus employing sacrificial coating on intermediate transfer member
WO2018082895A1 (en) * 2016-11-02 2018-05-11 Syngenta Participations Ag Agrochemical concentrates containing alkyl polyglucoside and non-ionic surfactant
KR102536880B1 (en) 2016-11-02 2023-05-24 신젠타 파티서페이션즈 아게 Pesticide Concentrate Containing Alkyl Polyglucosides and Nonionic Surfactants
JP2019532093A (en) * 2016-11-02 2019-11-07 シンジェンタ パーティシペーションズ アーゲー Pesticide concentrate containing alkyl polyglucoside and nonionic surfactant
IL266294B2 (en) * 2016-11-02 2024-05-01 Syngenta Participations Ag Agrochemical concentrates containing alkyl polyglucoside and non-ionic surfactant
CN109922658A (en) * 2016-11-02 2019-06-21 先正达参股股份有限公司 Agrochemical concentrate containing alkyl polyglycoside and nonionic surfactant
IL266294B1 (en) * 2016-11-02 2024-01-01 Syngenta Participations Ag Agrochemical concentrates containing alkyl polyglucoside and non-ionic surfactant
RU2757333C2 (en) * 2016-11-02 2021-10-13 Зингента Партисипейшнс Аг Agrochemical concentrates containing alkyl polyglucoside and non-ionic surfactant
AU2017355176B2 (en) * 2016-11-02 2022-03-31 Syngenta Participations Ag Agrochemical concentrates containing alkyl polyglucoside and non-ionic surfactant
KR20190082237A (en) * 2016-11-02 2019-07-09 신젠타 파티서페이션즈 아게 A pesticide concentrate containing an alkyl polyglucoside and a nonionic surfactant
US11464226B2 (en) 2016-11-02 2022-10-11 Syngenta Participations Ag Agrochemical concentrates containing alkyl polyglucoside and non-ionic surfactant
WO2019236723A1 (en) * 2018-06-05 2019-12-12 Monsanto Technology Llc Herbicidal compositions
CN115003157A (en) * 2020-01-10 2022-09-02 Upl有限责任公司 Stable agrochemical compositions and process for their preparation
WO2021140442A1 (en) * 2020-01-10 2021-07-15 UPL Corporation Limited A stable agrochemical composition and process for preparation thereof
US11478991B2 (en) 2020-06-17 2022-10-25 Xerox Corporation System and method for determining a temperature of an object
US11499873B2 (en) 2020-06-17 2022-11-15 Xerox Corporation System and method for determining a temperature differential between portions of an object printed by a 3D printer
US11498354B2 (en) 2020-08-26 2022-11-15 Xerox Corporation Multi-layer imaging blanket
US11767447B2 (en) 2021-01-19 2023-09-26 Xerox Corporation Topcoat composition of imaging blanket with improved properties

Also Published As

Publication number Publication date
CA2834789A1 (en) 2012-11-08
BR102012010651B8 (en) 2022-10-11
US11058108B2 (en) 2021-07-13
AR086284A1 (en) 2013-12-04
WO2012151455A1 (en) 2012-11-08
TN2013000457A1 (en) 2015-03-30
US20150024939A1 (en) 2015-01-22
IL229174A0 (en) 2013-12-31
AU2012250601B2 (en) 2015-07-16
CN103648274A (en) 2014-03-19
CN103648274B (en) 2017-02-08
NZ617125A (en) 2016-02-26
PL2704561T3 (en) 2017-05-31
MA35164B1 (en) 2014-06-02
EP2704561A1 (en) 2014-03-12
TW201247099A (en) 2012-12-01
EP2704561A4 (en) 2014-11-19
BR102012010651A2 (en) 2013-06-18
ES2592529T3 (en) 2016-11-30
CO6801801A2 (en) 2013-11-29
CA2834789C (en) 2019-07-09
EP2704561B1 (en) 2016-08-03
RU2013153904A (en) 2015-06-10
BR102012010651B1 (en) 2018-07-31
CL2013003129A1 (en) 2014-08-22
AU2012250601A1 (en) 2013-11-14
ZA201308084B (en) 2015-01-28
MX2013012893A (en) 2014-02-17
IL229174A (en) 2017-01-31

Similar Documents

Publication Publication Date Title
US11058108B2 (en) Stable high strength oil-in-water emulsions
EP3054774B1 (en) Aqueous herbicidal concentrates
MX2011004587A (en) Stable emulsifiable concentrates containing a first herbicidal carboxylic acid salt and a second herbicidal carboxylic acid ester.
US20230263158A1 (en) Pesticide emulsion concentrates containing natural or petroleum derived oils and methods of use
EP3131392B1 (en) Homogeneous aqueous pesticide concentrates containing paraffinic oils
CA2925412C (en) Aqueous herbicidal concentrates
NZ617125B2 (en) Stable high strength oil-in-water emulsions
WO2022118818A1 (en) Agrochemical composition
WO2022118817A1 (en) Agrochemical composition
CA3203804A1 (en) Liquid pesticidal formulation
CA3203806A1 (en) Liquid pesticidal formulation

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION