Classifications

• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N25/00—Biocides, 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
  • A01N25/24—Biocides, 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 ingredients to enhance the sticking of the active ingredients
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N25/00—Biocides, 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
  • A01N25/30—Biocides, 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
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N25/00—Biocides, 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
  • A01N25/02—Biocides, 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
  • A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
  • A01N25/06—Aerosols
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
  • A01N33/02—Amines; Quaternary ammonium compounds
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
  • A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
  • A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
  • A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
  • A01N37/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N39/00—Biocides, 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
  • A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
  • A01N39/04—Aryloxy-acetic acids; Derivatives thereof
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
  • A01N43/40—Biocides, 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
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
  • A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
  • A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
  • A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals

Definitions

• Spray drift during application can be reduced by incorporating certain tertiary amine or tertiary amine oxide surfactants into an aqueous herbicidal spray mixture containing glyphosate and an auxinic herbicide.
• Methods and compositions to reduce spray drift during the application of an aqueous herbicidal spray mixture are described herein.
• the methods to reduce spray drift during the application of an aqueous herbicidal spray mixture containing glyphosate and an auxinic herbicide include incorporating into the aqueous herbicidal spray mixture from about 0.02 to about 2 weight percent of one of a tertiary amine surfactant of the formula:
• aqueous concentrate compositions include from about 5 to about 40 weight percent of a water soluble salt of at least one auxinic herbicide, about 5 to about 40 weight percent of a water soluble salt of glyphosate, and from about 1 to about 20 weight percent of one or more tertiary amine or tertiary amine oxide.
• the methods and compositions reduce the amount of driftable fines of a herbicide spray in both aerial and ground spray applications.
• the methods include the use of compositions incorporating tertiary amine or tertiary amine oxide surfactants, or mixtures thereof, into aqueous herbicidal spray mixtures containing a water soluble glyphosate salt and at least one water soluble auxinic herbicide salt.
• Particularly useful auxinic herbicides to which this method applies include clopyralid, triclopyr, 2,4-D, 2,4-DB, MCPA, MCPB, dicamba, aminopyralid, and picloram.
• the methods described herein are most particularly useful for the application of herbicides that are subject to restricted applications around sensitive crops such as spray mixtures containing glyphosate and 2,4-D, triclopyr or dicamba.
• Suitable cations contained in the water soluble salt of glyphosate and the water soluble salt of the auxinic herbicide used in the spray mixtures described herein include isopropyl ammonium, dimethyl ammonium, triethyl ammonium, monoethanol ammonium, diethanol ammonium, triethanol ammonium, dimethylethanol ammonium, diethyleneglycol ammonium, triisopropanol ammonium, tetramethyl ammonium, tetraethyl ammonium, and choline.
• tertiary amine and tertiary amine oxide surfactants useful with the methods and compositions described herein may be prepared from petroleum derived raw materials or from naturally derived raw materials such as, for example, vegetable, animal, algae, or seed oils, or from combinations of petroleum derived or naturally derived raw materials.
• tertiary amine surfactants refer to trialkyl amines of the formula
• R 1 is a straight or branched chain (C 12 -C 18 ) alkyl and R 2 and R 3 independently are straight or branched chain (C 1 -C 18 ) alkyls.
• useful tertiary amine surfactants include those found in products such as, for example, Armeen® DMTD (cocoalkyldimethylamine; AkzoNobel, Chicago, Ill.) and the like.
• tertiary amine oxide surfactants refer to trialkyl amine oxides of the formula
• R 4 is a straight or branched chain (C 10 -C 18 ) alkyl or an alkyletherpropyl or alkylamidopropyl of the formula
• R 7 is a straight or branched chain (C 10 -C 18 ) alkyl
• R 5 and R 6 independently are straight or branched chain (C 1 -C 18 ) alkyl or ethoxylates or propoxylates of the formula
• n is an integer from 1 to 20, or mixtures thereof.
• useful tertiary amine oxide surfactants include those found in the following products such as, for example, Ammonyx® C (R 4 is cocoalkyl; R 5 and R 6 are methyl), Ammonyx® MO (R 4 is straight chain C 14 alkyl; R 5 and R 6 are methyl), Ammonyx® MCO (R 4 is indicated to be predominantly a mixture of straight chain C 14 and C 16 alkyls; R 5 and R 6 are methyl), Ammonyx® LO (R 4 is straight chain C 12 alkyl; R 5 and R 6 are methyl) and Ammonyx® CDO (R 4 is cocoamidopropyl; R 5 and R 6 are methyl) (the Ammonyx® line of products are available from Stepan Company, Northfield, Ill.); Rhodamox® LO (R 4 is indicated to be predominantly a mixture of straight chain C 12 and C 14 alkyls; R 5 and R 6 are methyl) (Rhodia-
• the tertiary amine or tertiary amine oxide surfactant, and mixtures thereof can be incorporated into the aqueous herbicidal spray mixture, for example, by being tank-mixed directly with the diluted herbicidal formulation.
• the tertiary amine or tertiary amine oxide surfactant, and mixtures thereof may be incorporated into the aqueous spray mixture at a concentration from about 0.02 to about 2 weight percent of the final spray mixture, preferably from about 0.05 to about 1.0 weight percent of the final spray mixture, and most preferably from about 0.05 to about 0.2 weight percent of the final spray mixture.
• the optimum spray droplet size depends on the application for which the composition is used. If droplets are too large, there will be less coverage by the spray; i.e, large droplets will land in certain areas while areas in between will receive little or no spray coverage.
• the maximum acceptable droplet size may depend on the amount of composition being applied per unit area and the need for uniformity in spray coverage. Smaller droplets provide more even coverage, but are more prone to drift during spraying. Thus, application parameters such as uniformity in spray coverage must be balanced against the tendency for smaller droplets to drift. For example, if it is particularly windy during spraying, larger droplets may be needed to reduce drift, whereas on a calmer day smaller droplets may be acceptable.
• spray droplet size may also depend on the spray apparatus, e.g., nozzle size and configuration.
• the reduction in spray drift may result from a variety of factors including a reduction in the production of fine spray droplets ( ⁇ 150 ⁇ m minimum diameter) and an increase in the volume median diameter (VMD) of the spray droplets.
• the median diameter of the plurality of spray droplets created using the compositions and methods described herein is increased above that of a spray composition that does not include the tertiary amine or tertiary amine oxide surfactants as described herein.
• aqueous concentrate compositions are also described.
• aqueous concentrate compositions are solutions containing high concentrations of the aqueous herbicidal spray components described above, i.e., a water soluble glyphosate salt, one or more water soluble auxinic herbicide salts, and one or more tertiary amine or tertiary amine oxide surfactants.
• the aqueous concentrate compositions are intended to be diluted to provide aqueous herbicidal spray mixtures for use, for example, with the methods described herein.
• the aqueous concentrate compositions include from about 5 to about 40 weight percent of one or more water soluble salts of an auxinic herbicide, from about 5 to about 40 weight percent of a water soluble salt of glyphosate, and from about 1 to about 20 weight percent of one or more tertiary amine or tertiary amine oxide surfactants.
• the aqueous concentrate compositions are preferably solutions containing the one or more tertiary amine or tertiary amine oxide surfactant, or mixtures thereof, dissolved or dispersed in the formulation containing the auxinic herbicide and glyphosate.
• the aqueous concentrate compositions contain about 10 to about 40 weight percent of the water soluble glyphosate salt; about 10 to about 40 weight percent of the one or more water soluble auxinic herbicide salts; and about 1 to about 18, about 1 to about 16, about 1 to about 14, about 1 to about 12, about 1 to about 10, about 1 to about 9, about 1 to about 8, about 1 to about 7, about 1 to about 6, about 1 to about 5, about 1 to about 4, about 1 to about 3, about 1 to about 2, or about 1 to about 1.5 weight percent of the one or more tertiary amine or tertiary amine oxide surfactants.
• the aqueous concentrate compositions contain about 15 to about 30, about 20 to about 30, or about 25 to about 30 weight percent of the water soluble glyphosate salt; about 15 to about 30, about 20 to about 30, or about 25 to about 30 weight percent of the one or more water soluble auxinic herbicide salts; and about 1 to about 18, about 1 to about 16, about 1 to about 14, about 1 to about 12, about 1 to about 10, about 1 to about 9, about 1 to about 8, about 1 to about 7, about 1 to about 6, about 1 to about 5, about 1 to about 4, about 1 to about 3, about 1 to about 2, or about 1 to about 1.5 weight percent of the one or more tertiary amine or tertiary amine oxide surfactants.
• the aqueous concentrate compositions can be stored in suitable containers as will be readily recognized by one of skill in the art and can be, for example, solutions, emulsions, or suspensions.
• Aqueous solutions i.e., including both concentrates and spray solutions, containing 2,4-D and glyphosate are prone to incompatibility under certain conditions and concentrations leading to product performance issues and difficulty in using the products, i.e., difficulty with field applications of the products.
• Incompatibility in concentrate compositions is minimized by the use of very small amounts of 2,4-D, such as less than about 3 wt % ae (acid equivalent) relative to the total composition.
• compositions described herein may contain surfactants in addition to the tertiary amine and tertiary amine oxide surfactants mentioned herein.
• the additional surfactants may be anionic, cationic, or nonionic in character.
• typical surfactants include alcohol-alkylene oxide addition products, such as tridecyl alcohol-C 16 ethoxylate; sorbitol esters, such as sorbitol oleate; quaternary amines, such as lauryl trimethylammonium chloride; ethoxylated amines, such as tallowamine ethoxylated; betaine surfactants, such as cocoamidopropyl betaine; fatty acid amidopropyl dimethylamine surfactants such as cocoamidopropyl dimethylamine; alkylpolyglycoside surfactants; polyethylene glycol esters of fatty acids, such as polyethylene glycol stearate; block copolymers of ethylene oxide and propylene oxide; salt
• compositions optionally containing one or more additional compatible ingredients are provided herein.
• additional ingredients may include, for example, one or more pesticides or other ingredients, which may be dissolved or dispersed in the composition and may be selected from acaricides, bactericides, fungicides, insecticides, herbicides, herbicide safeners, insect attractants, insect repellents, plant activators, plant growth regulators, and synergists.
• any other additional ingredients providing functional utility such as, for example, dyes, stabilizers, fragrants, viscosity-lowering additives, compatibility agents, and freeze-point depressants may be included in these compositions.
• Herbicide concentrates containing 228 grams acid equivalent per liter (g ae/L) 2,4-D choline, 240 g ae/L glyphosate dimethyl ammonium (DMA), 60 g/L propylene glycol, and 36 g/L (dry weight basis) of the indicated tertiary amine oxide surfactants were prepared as described below using the following aqueous samples of the amine oxide surfactants:
• a 50 milliliter (mL) volumetric flask was first charged with 23.58 g of a 48.35 wt % ae of a 2,4-D choline salt solution in water. To the volumetric flask, 3.00 g of propylene glycol was added and the liquids were then blended by hand shaking the flask until the contents were homogenous. Next, 24.52 g of a 48.95 wt % ae of a glyphosate DMA solution in water was added to the flask. The volumetric flask was once again hand shaken until the contents were blended and homogenous.
• the tertiary amine oxide surfactant was added (3.60 g of Aromox® C/12 solution; 6.00 g for all others) and the flask was hand shaken until the contents were blended and homogenous.
• deionized water was added to fill the volumetric flask to the 50 mL mark. The sample was then blended by shaking the solution by hand until the liquid was homogenous. Seven samples containing one each of the tertiary amine oxide surfactants listed above and one concentrate containing no tertiary amine oxide surfactant (i.e., control sample) were prepared in this manner.
• Each of the herbicide concentrates were then diluted in water to make a 2.49% v/v spray solution of each by taking 11.21 mL of the herbicide concentrate, placing it into 438.80 mL of deionized water and then lightly shaking by hand until each spray sample was homogenous.
• the eight spray solutions were sprayed using a Teejet® 8002 flat fan nozzle (Teejet Technologies; Wheaton, Ill.) at 40 psi (276 kiloPascal) and the spray droplet size distribution measurement was performed with a Sympatec Helos/KF high resolution laser diffraction particle sizer with an R7 lens (Sympatec GmbH; Clausthal-Zellerfeld, Germany).
• the tip of the nozzle was situated 12 inches (30.5 centimeters) above the path of the laser beam of the Sympatec particle sizer.
• the percentage of driftable fines was expressed as the volume percentage of spray droplets below 150 ⁇ m volume mean diameter (VMD) as shown in Table 1.
• Herbicide concentrates containing 114 g ae/L 2,4-D DMA, 120 g ae/L glyphosate DMA, 30 g/L propylene glycol, and 18 g/L (dry weight basis) of the tertiary amine oxide surfactants listed in Example 1 were prepared as follows. A 100 mL volumetric flask was first charged with 20.56 g of a 55.44 wt % ae 2,4-D DMA salt solution in water. To the volumetric flask, 3.00 g of propylene glycol was added and the liquids were then blended by hand shaking the flask until the contents were homogenous.
• Each of the herbicide concentrates was then diluted in water to make a 4.99% v/v spray solution of each by taking 22.46 mL of the herbicide concentrate and placing it into 427.55 mL of deionized water and then lightly shaking by hand until each spray sample was homogenous.
• the eight spray solutions were sprayed using the same procedure and technique described in Example 1. The results are shown in Table 2.
• a tank-mixed spray solution containing dicamba diglycol ammonium (DGA) salt, glyphosate isopropyl ammonium (IPA) salt, and a tertiary amine oxide surfactant was prepared.
• a sample container was first charged with 276.73 mL of deionized water and then 4.56 g of 30% w/w Ammonyx® LO solution was added and mixed.
• 11.22 mL of Rodeo® herbicide concentrate commercial 4 pounds acid equivalent per gallon (lb ae/gal) glyphosate IPA salt solution from Dow AgroSciences, LLC) and 7.49 mL of Clarity® herbicide concentrate (commercial 4 lb ae/gal dicamba DGA salt solution from BASF
• TAA Triclopyr Triethyl Ammonium
• IPA Glyphosate Isopropyl Ammonium
• a tank-mixed spray solution containing triclopyr triethyl ammonium (TEA) salt, glyphosate isopropyl ammonium (IPA) salt, and a tertiary amine oxide surfactant was prepared.
• a sample container was first charged with 275.48 mL of deionized water and then 0.79 g of 30% w/w Ammonyx® LO solution was added and mixed.
• Rodeo® herbicide concentrate commercial 4 lb ae/gal glyphosate IPA salt solution from Dow AgroSciences, LLC
• Garlon 3A® herbicide concentrate commercial 3 lb ae/gal triclopyr TEA salt solution from Dow AgroSciences, LLC
• Table 4 The results, along with that for a control spray sample containing no tertiary amine oxide surfactant are shown in Table 4.
• a herbicide concentrate containing 225 g ae/L of 2,4-D DMEA (dimethylethanol ammonium), 225 g ae/L of glyphosate DMA, 51 g/L of propylene glycol, and 56 g/L of Armeen® DMTD dimethyltallowalkylamine (AzkoNobel; Chicago, Ill.) was prepared as follows: 14.72 mL of a glyphosate DMA stock solution (40.5 wt % ae, density-1.208 g/mL), 14.98 mL of a 2,4-D DMEA/propylene glycol stock solution (40.3 wt % ae 2,4-D DMEA, 9.1 wt % propylene glycol, density-1.192 g/mL), and 2.25 mL (1.80 g, density-0.80 g/mL) of Armeen® DMTD were combined and swirled to yield a clear, homogeneous concentrate.
• the resulting herbicide concentrate was then diluted in deionized water to make a 4% (vol/vol) spray solution in a similar manner as described in Example 1.
• the spray solution was sprayed using the same procedure and technique described in Example 1. The results are shown in Table 5.
• a glyphosate/2,4-D concentrate formulation was prepared by blending 22.01 g of 2,4-D choline concentrate (44.30 wt % acid equivalent (ae)), 3.0 g propylene glycol, 21.22 g of glyphosate DMA concentrate (48.30 wt % ae), 3.53 g of Tomamine® AO-728 Special (50% active linear alkylpropylamine oxide, 1.77 g active; AirProducts; Allentown, Pa.), and sufficient water to charge a 50 mL volumetric flask.
• the formulation contained 205 g/L glyphosate DMA (ae) and 195 g/L 2,4-D choline (ae).
• the resulting herbicide concentrate was then diluted in deionized water to make a 4.38% (vol/vol) spray solution in a similar manner as described in Example 1.
• the spray solution was sprayed using the same procedure and technique described in Example 1. The results are shown in Table 6.

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  • 2011-09-15 BR BR122017003656-4A patent/BR122017003656B1/pt active IP Right Grant
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