US20170172142A1 - Polyelectrolyte-layer forming block copolymers and compositions and uses thereof - Google Patents

Polyelectrolyte-layer forming block copolymers and compositions and uses thereof Download PDF

Info

Publication number
US20170172142A1
US20170172142A1 US15/373,664 US201615373664A US2017172142A1 US 20170172142 A1 US20170172142 A1 US 20170172142A1 US 201615373664 A US201615373664 A US 201615373664A US 2017172142 A1 US2017172142 A1 US 2017172142A1
Authority
US
United States
Prior art keywords
composition
block copolymer
moiety
polyelectrolyte
particles
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
US15/373,664
Other languages
English (en)
Inventor
Gilad Silbert
Michael Berkovitch
David James Wilson
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.)
Rhodia Operations SAS
Adama Makhteshim Ltd
Original Assignee
Rhodia Operations SAS
Adama Makhteshim Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Rhodia Operations SAS, Adama Makhteshim Ltd filed Critical Rhodia Operations SAS
Priority to US15/373,664 priority Critical patent/US20170172142A1/en
Publication of US20170172142A1 publication Critical patent/US20170172142A1/en
Assigned to RHODIA OPERATIONS reassignment RHODIA OPERATIONS ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: WILSON, DAVID JAMES
Assigned to ADAMA MAKHTESHIM, LTD. reassignment ADAMA MAKHTESHIM, LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BERKOVITCH, Michael, SILBERT, Gilad
Priority to US16/653,595 priority patent/US11533910B2/en
Priority to US17/946,610 priority patent/US20230067163A1/en
Assigned to RHODIA OPERATIONS reassignment RHODIA OPERATIONS ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: WILSON, DAVID JAMES
Abandoned legal-status Critical Current

Links

Images

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
    • A01N25/02—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
    • 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
    • A01N25/12—Powders or granules
    • 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
    • A01N25/26—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 in coated particulate form
    • 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
    • A01N29/00—Biocides, pest repellants or attractants, or plant growth regulators containing halogenated hydrocarbons
    • 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
    • A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
    • A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
    • A01N41/10—Sulfones; Sulfoxides
    • 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
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/707—1,2,3- or 1,2,4-triazines; Hydrogenated 1,2,3- or 1,2,4-triazines
    • 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
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
    • 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
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
    • 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
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
    • A01N47/04—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing >N—S—C≡(Hal)3 groups
    • 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
    • A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring
    • 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
    • A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/10—Fluorides
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
    • C08G81/02—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C08G81/021—Block or graft polymers containing only sequences of polymers of C08C or C08F
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
    • C08G81/02—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C08G81/024—Block or graft polymers containing sequences of polymers of C08C or C08F and of polymers of C08G
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/02—Emulsion paints including aerosols
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/65—Additives macromolecular
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/42—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
    • C09K8/46—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement
    • C09K8/467—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement containing additives for specific purposes
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2103/00—Function or property of ingredients for mortars, concrete or artificial stone
    • C04B2103/0045—Polymers chosen for their physico-chemical characteristics
    • C04B2103/0059—Graft (co-)polymers
    • C04B2103/006—Comb polymers
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2103/00—Function or property of ingredients for mortars, concrete or artificial stone
    • C04B2103/0045—Polymers chosen for their physico-chemical characteristics
    • C04B2103/0061—Block (co-)polymers

Definitions

  • the present invention relates generally to polyelectrolyte-layer forming block copolymers adsorbed at colloid interfaces in aqua solution and compositions and uses thereof.
  • the present invention relates to agricultural material compositions comprising particles of at least one agricultural material compound and a polyelectrolyte-layer forming block copolymer.
  • the present invention also relates to non-agricultural material compositions comprising particles of at least one non-agricultural material compound and a polyelectrolyte-layer forming block co-polymer.
  • water based formulations are composed of the hydrophobic solid particles of the AI suspended in the aqua phase or hydrophobic drops and capsules, which contain the active ingredient, dispersed in the water.
  • the concentration of a pesticide active material and other materials for agricultural application in a formulation can influence the application rate and packaging of the product.
  • High-load formulations require less packaging and thus are easier to handle and transport.
  • the ultimate goal for designing a pesticidal formulation is to prepare the formulation with the highest possible amount of the active material, with the resultant formulation maintaining stability and a long shelf life, and also providing an environmentally friendly and cheaper product.
  • dispersing agents and surfactants are known in the art to achieve these purposes.
  • the dispersing agents in this regard can be ionic or non-ionic compounds, polymeric or non-polymeric surfactants. Some of these co-formulants impart rheology properties for the concentrated pesticidal formulations.
  • the dispersant surrounds the particles and disperses the particles in the liquid phase and therefore prevents and/or breaks aggregates.
  • Previously exemplified and known dispersants useful in this regard include comb co-polymers such as AtloxTM 4913, block co-polymers of alkylene oxide, ethoxylate alcohol and anionic type polymers such as fatty acid sulfonate.
  • dispersants In order to achieve and stabilize a high load formulation there is a need for the dispersants to stabilize extremely well against flocculation and coagulation, to perform well at low concentration of dispersant and to reduce the friction between the particles. In granulation processes, good lubricating properties of the dispersant are also desired. Another important property for a dispersant is good performance in both high and low concentrations of the electrolyte.
  • WO 2015116716 is directed to compositions for plant growth regulation comprising at least one polyanionic polymer in combination with one or more plant growth regulators, in preferred forms, the polyanionic polymer comprises a copolymer polymers having repeat units randomly located along the polymer chain without any ordered sequence of repeat units.
  • WO 2013004704 discloses, in part, an apolar liquid comprising micelles comprising a copolymer AB, in which the micellar cores are more hydrophilic than the micelle coronas.
  • the copolymer is formed as micelles in a water-free organic solvent liquid medium to provide a surface coating.
  • WO 2013189776 discloses a solid dispersion consisting of hydrophobic active ingredients and cationic copolymers of N,N-diethylaminoethyl methacrylate and methyl methacrylate, the monomers being provided at a weight ratio of 35:65 to 55:45.
  • compositions comprising a polyelectrolyte complex of a polyanion, preferably selected from the group consisting of a natural polyanion such as xanthan gum, alginate, a lignin compound such as lignosulfonate, pectin, carrageenan, humic acid, fulvic acid, angico gum, gum Kondagogu, sodium alkyl naphtalene sulfonate, poly- ⁇ -glutamic acid, maleic starch half-ester, carboxymethyl cellulose, chondroitin sulphate, dextran sulphate, hyaluronic acid, and a synthetic polyanion such as poly(acrylic acid), polyphosphoric acid, and poly(L-lactide), and a polycation preferably selected from the group consisting of poly-L-lysine, epsilon-poly-L-lysine, poly-L-arginine, chitosan oligosacc
  • WO 2013093578 discloses a polymer selected from the group consisting of poly(methacrylic acid-co-ethyl acrylate); poly(methacrylic acid-co-styrene); poly(methacrylic acid-co-butylmethacrylate); poly[acrylic acid-co-poly(ethylene glycol) methyl ether methacrylate]; and poly(n-butylmethacrylcate-co-methacrylic acid).
  • any known dispersants as described by the prior art are limited in some of the characteristics needed for a dispersant to achieve a high load formulation: stabilization against agglomeration, reduction in the friction between particles, perform well at low concentration and efficient in different electrolyte solutions.
  • the prior art typically provides products with the amount of particles present being limited. Accordingly, there remains a need in the art for pesticidal compositions containing improved dispersants which permit a higher concentration of the active ingredient in the composition, and which enable improved milling and granulation of the composition.
  • the present subject matter relates to the use of a polyelectrolyte-layer forming block copolymer as a dispersant or emulsifier wherein the block copolymers adsorb on the surfaces of the active ingredient particles in a dispersion to result in a stable brushed “particle-polymer” complex.
  • the present compositions have a reduced friction between particles and stabilize dispersions in a very efficient way. Also, by combining steric and ionic stabilization they perform well at both high and low concentrations of electrolytes.
  • the subject invention provides an agricultural material composition comprising:
  • the subject invention provides a pesticidal composition comprising:
  • the subject invention also provides a method of controlling and preventing pest comprising applying a pesticidal composition to a locus where the pest is to be controlled and prevented, wherein the pesticidal composition comprises:
  • the subject invention also provides a method of improving plant growth comprising applying an agricultural material composition to at least one of a plant, an area adjacent to a plant, soil adapted to support growth of a plant, a root of a plant, foliage of a plant, and/or a seed adapted to produce a plant, wherein the composition comprises:
  • the subject invention also provides a process of preparing a composition comprising mixing particles of at least one compound with an amount of a polyelectrolyte-layer forming block co-polymer, wherein the block copolymer comprises (A) an anchoring moiety and (B) at least one stabilizing moiety.
  • the subject invention also provides a process of preparing a pesticidal composition comprising mixing particles of at least one pesticide compound with an amount of a polyelectrolyte-layer forming block co-polymer, wherein the block copolymer comprises (A) an anchoring moiety and (B) at least one stabilizing moiety.
  • the subject invention also provides a colorant system composition comprising:
  • the subject invention also provides an aqueous non-agricultural-application-based composition comprising at least:
  • the subject invention also provides a method of preparing a coating composition comprising contacting a film forming polymer latex with a dispersant system comprising a polyelectrolyte-layer forming block copolymer, wherein the block copolymer comprises (A) an anchoring moiety and (B) at least one stabilizing moiety.
  • the subject invention also provides a method of preparing a colorant system composition
  • a method of preparing a colorant system composition comprising contacting a colorant component with a dispersant system comprising a polyelectrolyte-layer forming block copolymer wherein the block copolymer comprises (A) an anchoring moiety and (B) at least one stabilizing moiety, and wherein the resulting colorant system composition is a dispersion.
  • the subject invention also provides a method of tinting an alkyd-based base coating or a latex-based base coating comprising contacting the alkyd-based base coating or the latex-based base coating with a colorant system composition, wherein the colorant system composition comprises:
  • the subject invention also provides an oil cement grout composition
  • an oil cement grout composition comprising solid particles and a polyelectrolyte-layer forming block copolymer wherein the block copolymer comprises (A) an anchoring moiety and (B) at least one stabilizing moiety.
  • the subject invention also provides use of a polyelectrolyte-layer forming block copolymer comprising (A) an anchoring moiety and (B) at least one stabilizing moiety for keeping solid particles in suspension in an oil cement grout composition.
  • FIG. 1 shows the change in the viscosity between the milling steps for formulation 1, without the presently described polymer, and for formulation 2, with the presently described polymer.
  • FIG. 2 shows the change in the particle size distribution during the milling steps in the production process.
  • FIGS. 3A and 3B provides a comparison of performances of known dispersants and of the presently described polymer dispersant in high salt solutions.
  • FIG. 4 provides a comparison of performances of additional known dispersants and of the presently described polymer dispersant in high salt solutions.
  • FIGS. 5A and 5B provide a comparison of performances of further known dispersants and of the presently described polymer dispersant in high salt solutions.
  • FIG. 6 shows the viscosities during the milling of Formulation 3 and Formulation 2.
  • FIG. 7 shows the general structure of a di-block copolymer.
  • FIG. 8 shows the general structure of a tri-block copolymer.
  • FIG. 9 shows the general structure of a comb-graft polymer/copolymer.
  • agricultural material means an active ingredient used in the practice of farming, including cultivation of the soil for the growing of crops.
  • use of agricultural materials is not limited to application to crops.
  • Agricultural materials may be applied to any surface, e.g., for the purpose of cleaning or aiding or inhibiting growth of a living organism.
  • Other non-crop applications include, but are not limited to, application to an animal, e.g. livestock, application to turf and ornamentals, and application to railroad weed.
  • agrochemical is a chemical active ingredient used in the practice of farming, including cultivation of the soil for the growing of crops.
  • use of agrochemicals is not limited to application to crops.
  • Agrochemicals may be applied to any surface, e.g., for the purpose of cleaning or aiding or inhibiting growth of a living organism.
  • agricultural materials and agrochemicals include, but are not limited to, pesticides, hormones, bio-stimulants, and plant growth agents.
  • the term “pesticide”, “pesticide compound” or “pesticidal compound” means a compound capable of killing or inhibiting growth or proliferation of a pest, whether for plant protection or for non-crop application. As used herein, all “pesticide”, “pesticide compound” or “pesticidal compound” fall within “agricultural material compound”.
  • the term “pesticide”, “pesticide compound” or “pesticidal compound” includes, but is not limited to, insecticide, nematicide, herbicide, fungicide, algicides, animal repellents, and acaricides.
  • the term “pest” includes, but is not limited to, insect, nematode, weed, fungi, algae, mite, tick, and animal.
  • the term “weed” refers to any unwanted vegetation.
  • hydrophobic when used to characterize a compound or a surface means that the compound or surface lacks affinity for water.
  • polyelectrolyte means a polymer which contains charged monomers.
  • block copolymer means a polymer comprising at least two different polymers combined by a covalent bond.
  • Each of the blocks is usually a homopolymer but can also be a copolymer with a specific distinct physical/chemical or functional characteristic (e.g., having one block that is easily soluble in water, with the other block being primarily insoluble in water).
  • anchoring block means a block comprised of a homopolymer or copolymer which has an affinity for the particle surface and which will cause the block copolymer to adsorb strongly and even irreversibly to the particle surface.
  • stabilizing block means a charged polymer zone for which the dispersing medium, ex. water, is a good solvent. More specifically, if a copolymer is prepared of same molar mass and composition as that of the stabilizing block, then it should be soluble in the dispersing medium at a concentration greater than or equal to 10 wt %, for instance greater than or equal to 20 wt %, for instance greater than or equal to 30 wt %, for instance greater than or equal to 40 wt %, for instance greater than or equal to 50 wt %, for instance greater than or equal to 60 wt % and even 80 wt %.
  • comb copolymer means polymers wherein side polymeric chains are bonded to a polymer/copolymeric main chain, frequently also known as the backbone.
  • the present polymer/copolymers have at least one repeat unit derived from polyolefin-based macromonomers.
  • the term “dispersion” means a formulation which includes a heterogeneous mixture of at least two phases wherein the first (continuous phase) is liquid and the second (dispersed phase) is solid or liquid particles.
  • the “dispersion” compositions discussed herein necessarily include an aqueous phase as the continuous phase.
  • suspension and “dispersion” are interchangeable and means a formulation having solid particles that are mixed with at least one liquid phase but which remain undissolved. Water is the continuous phase.
  • capsule suspension means a formulation having solid capsules contained active ingredient, surrounding by a solid coating, dispersed in water.
  • particle As used herein, the terms “particle”, “solid particle”, “liquid droplets” and capsules can be used interchangeably to mean solids and/or drops.
  • particles having a “brushed structure” have a layer of polymers attached on one end to the surface of the particles and on the other end extend normal to the surface into a bulk solution.
  • agriculturally acceptable carrier means carriers, which are known and accepted in the art for the formation of formulations for agricultural or horticultural use.
  • the phrase “ultra-high concentration” and “high-load concentration” means active substances in amounts of at least 500 g/L.
  • the term “high salt environment” means that the composition contains at least 5% by weight of salt relative to the weight of the composition.
  • the composition may also contain at least 7% by weight of salt or at least 10% by weight of salt relative to the total weight of the composition.
  • the subject invention provides an agricultural material composition comprising:
  • the subject invention provides a pesticidal composition comprising:
  • the block copolymer is adsorbed at the interface between the hydrophobic surface of the particles and the water. When surrounded in a water medium, the block copolymer hydrates, leading to a highly efficient lubrication.
  • the particles are dispersed in the water.
  • the resultant particles of the combination of the polyelectrolyte-layer formed through the block copolymer and the active ingredient has a brushed structure. In water, the brushed polyelectrolyte layer is hydrated, resulting in a highly efficient lubrication.
  • the composition is a dispersion.
  • the agricultural material is an agrochemical.
  • the agricultural material is a plant growth regulator. In one embodiment, the agricultural material is a bio-stimulant. In one embodiment, the agricultural material is a hormones.
  • the agricultural material is a pesticide.
  • the pesticide is an insecticide. In one embodiment, the pesticide is a nematicide. In one embodiment, the pesticide is an herbicide. In one embodiment, the pesticide compound is a fungicide. In one embodiment, the pesticide is an algicide. In one embodiment, the pesticide is an animal repellent. In one embodiment, the pesticide is an acaricide.
  • herbicides may include, but are not limited to, atrazine, diuron, chlorotoluron, clethodim, clomazone, and tebuthiuron.
  • insecticides and acaricides may include, but are not limited to, abamectin, pyriproxyfen, acetamiprid, bifenthrin, cyfluthrin, pymetrozine, novaluron, ethiprole, fipronil, and lambda-cyhalothrin.
  • fungicides may include, but are not limited to, azoxistrobine, chlorothalonil, epoxiconazole, propiconazole, fenpropidin, folpet, epoxiconazole, tebuconazole, cyprodinil, diazinon, dimethomorph, fipronil, fludioxonil, and captan.
  • nematicide may include, but not limited to, fluensulfone.
  • the agricultural material is hydrophobic agricultural material.
  • the agricultural material is hydrophobic agrochemical.
  • the agricultural material is hydrophobic pesticide.
  • the particles of the at least one agricultural material compound is hydrophobic particles.
  • the particles are in solution which comprises the agricultural material.
  • the particles are solid.
  • the particles are liquid.
  • the particles are capsules.
  • the particles are drops.
  • the drops are agricultural material which is dissolved in the solvent.
  • the drops are pesticide which is dissolved in the solvent.
  • the particles are agricultural material which is dissolved in the solvent.
  • the particles are pesticide which is dissolved in the solvent.
  • the particles are agricultural material which is encapsulated.
  • the particles are pesticide which is encapsulated.
  • the drops are in solution which comprises the agricultural material.
  • the agricultural material is liquid.
  • the agricultural material is dissolved in solvent.
  • the solvent is non aqueous solvent.
  • the solvent is organic solvent.
  • Solvents may include, but are not limited to, methyloleate (Agnique® ME 181), aromatic fluids (SolvessoTM), cyclohexanon, N,N-dimethyloctanamide, N,N-dimethyl-decanamide, acetophenone, and octanol.
  • the composition further comprises an agriculturally acceptable carrier. In one embodiment, the composition further comprises a safener. In one embodiment, the composition further comprises a preservative. In another embodiment, the composition further comprises at least one additional component/moiety selected from the group consisting of surfactants, rheology modifiers, anti-settling agents, antifoam agents, buffers, and liquid diluents. Other ingredients, such as wetting agents, adhesives, thickeners, binders, colorants such as azo, phthalocyanine or other pigments, or antifreeze agents, may also be added to the composition in order to increase the stability, density, appearance and ease-of-handling of the composition.
  • the agricultural material composition can further comprise adjuvant such as ionic, anionic, nonionic, polymeric/copolymeric, or non-polymeric/copolymeric surfactants.
  • adjuvant such as ionic, anionic, nonionic, polymeric/copolymeric, or non-polymeric/copolymeric surfactants.
  • One exemplary moiety in this regard can be a penetrant amassment such as a pyrrolidone.
  • the composition is an emulsion, a suspension, a suspension concentrate, a capsule suspension, or a suspo-emulsion.
  • the composition is an emulsion and the emulsion is an oil in water emulsion.
  • the polyelectrolyte layer adsorbed on the surface of the droplets containing at least one agricultural material compound and stabilizes the droplets as the oil phase of a dispersion, wherein at least one agricultural material compound is in the oil phase and is dispersed in a continuous water phase.
  • the present dispersions can maintain a high concentration of oil while preserving the oil in water emulsion system. This permits the emulsion to remain stable, and prevents the inversion of the oil and water phases.
  • the oil in water emulsion comprises at least 40, 50, 60, or 70% by weight of an oil phrase.
  • the composition is an aqueous suspension.
  • the aqueous suspension has a concentration of greater than 500 g/L of particles of the agricultural material compound. In one embodiment, the aqueous suspension has a concentration of between 900 g/L to 1200 g/L of particles of the agricultural material compound. In one embodiment, the suspension has a viscosity of less than 750 cPs. In one embodiment, the suspension contains no thickening agent and has a viscosity of less than 750 cPs. Viscosity is measured using the Brookfield viscometer at spindle 62 and 12 RPM.
  • the composition is a suspension concentrate.
  • the suspension concentrate further comprises a nonionic surfactant, an anionic surfactant, and/or an anti-crystallization agent (crystal growth inhibitor).
  • the composition is in solid form. In one embodiment, the solid composition is in the form of granules.
  • the subject invention also provides a method of controlling and preventing pest comprising applying a pesticidal composition to a locus where the pest is to be controlled and prevented, wherein the pesticidal composition comprises:
  • the pest is insect. In one embodiment, the pest is fungi. In one embodiment, the pest is nematode. In one embodiment, the pest is weed.
  • the locus is a plant, an area adjacent to a plant, soil adapted to support growth of a plant, a root of a plant, foliage of a plant, and/or a seed adapted to produce a plant.
  • the present compositions may be applied to healthy or diseased plant.
  • the present compositions is applied to various plants including but not limited to crops, seeds, bulbs, propagation material, turf, or ornamental species.
  • the locus is a wall, a floor, or a surface of a furniture or fixture. In one embodiment, the locus is a kitchen surface or bathroom surface.
  • the locus is skin of an animal or surrounding of an animal. In one embodiment, the locus is a railway or an area surrounding a railway.
  • compositions can be diluted and applied in a customary manner, for example by watering (drenching), drip irrigation, spraying, and/or atomizing.
  • the subject invention also provides a method of improving plant growth comprising applying an agricultural material composition to at least one of a plant, an area adjacent to a plant, soil adapted to support growth of a plant, a root of a plant, foliage of a plant, and/or a seed adapted to produce a plant, wherein the composition comprises:
  • the agricultural material is a plant growth regulator. In one embodiment, the agricultural material is a bio-stimulant. In one embodiment, the agricultural material is a hormone.
  • the method is effective to increase yield of the plant. In one embodiment, the method is effective to increase growth rate of the plant. In one embodiment, the method is effective to increase size of the plant.
  • the present compositions is applied to various plants including but not limited to crops, seeds, bulbs, propagation material, or ornamental species.
  • compositions can be diluted and applied in a customary manner, for example by watering (drenching), drip irrigation, spraying, and/or atomizing.
  • the agricultural material composition is high-load. In some embodiments of the subject invention, the pesticidal composition is high-load.
  • the high-load composition is a dispersion. In one embodiment, the high-load composition is prepared as a stable, accurate-to-dilute, easy-to-dilute concentrated dispersion.
  • the concentration of particles in the composition is 500, 600, 700, 800, 900, 1000, 1100, or 1200 g/L. In another embodiment, the concentration of particles in the composition is 900-1200 g/L.
  • the density of the composition is about 1.4-1.6 kg/L. Dispersible compositions of this density provide enhanced stability of formulations with closed packed particles in the composition.
  • the composition comprises about 15-40% by weight of water.
  • the viscosity of the composition is less than 750 cPs. Viscosity measured at spindle 62 and 12 RPM using Brookfield viscometer.
  • compositions are advantageous because they contain densely packed particles, yet maintain low viscosity and high flowability. These compositions can also have a high particle concentration and very small amounts of water.
  • the present high-load compositions are also advantageous because they permit a reduction of package volume of the composition comprising at least one compound.
  • the at least one compound is an agricultural material compound.
  • the agricultural material compound is an agrochemical compound.
  • the agricultural material compound is a pesticide compound.
  • the agricultural material compound is a plant growth regulator, a hormone, or a bio-stimulant.
  • the at least one compound is a non-agricultural material compound.
  • the present invention provides a process of preparing a composition comprising mixing particles of at least one compound with an amount of a polyelectrolyte-layer forming block co-polymer, wherein the block copolymer comprises (A) an anchoring moiety and (B) at least one stabilizing moiety.
  • the present invention provides a process of preparing a pesticidal composition comprising mixing particles of at least one pesticide compound with an amount of a polyelectrolyte-layer forming block co-polymer, wherein the block copolymer comprises (A) an anchoring moiety and (B) at least one stabilizing moiety.
  • mixing comprises preparing a dispersion of particles of the at least one compound and adsorbing the polyelectrolyte-layer forming block copolymer on hydrophobic surfaces of the particles to form a polyelectrolyte layer on the particle interface.
  • mixing comprises preparing a dispersion comprising particles in up to 20% w/w water of the at least one compound and adsorbing the polyelectrolyte-layer forming block copolymer on hydrophobic surfaces of the particles in the dispersion and forming a polyelectrolyte layer on the particle interface.
  • the present invention provides a process of preparing a pesticidal composition comprising:
  • the dispersion is a water dispersion. In one embodiment, the dispersion has a concentration of agricultural material particles of at least 900 g/L.
  • the process further comprises a wet milling step after the polyelectrolyte layer is formed.
  • the amount of the block copolymer is effective to reduce the temperature during milling of the composition compared to the temperature during milling of the same composition without addition of the block co-polymer.
  • the amount of block copolymer is effective to reduce the viscosity of the composition during milling of the composition compared to the viscosity of the same composition during milling without addition of the block co-polymer.
  • the temperature during the wet milling process is less than 30° C. In one embodiment, the temperature during milling is reduced from 40° C.-50° C. to 20° C.-25° C. In one embodiment, the viscosity during milling is reduced from 1000-2000 cPs to 200-400 cPs. Viscosity is measured using the Brookfield viscometer at spindle 62 and 12 RPM. In yet another specific embodiment, 90% of the particles have a particle size of 50 ⁇ m or greater prior to the wet milling process and a particle size of 1 ⁇ m or less after the wet milling process.
  • the process further comprises a granulation step after the polyelectrolyte layer is formed.
  • the preparation provides an improved granulation by reducing the pressure that develops during granulation.
  • the amount of block copolymer is effective to reduce the pressure during granulation of the composition compared to the pressure during granulation of the same composition without addition of the block co-polymer.
  • the subject invention provides a method of reducing pressure during granulation of a composition comprising at least one compound by adding an amount of a polyelectrolyte-layer forming block copolymer to the composition, wherein the block copolymer comprises (A) an anchoring moiety and (B) at least one stabilizing moiety, and wherein the amount of block copolymer is effective to reduce the pressure during granulation of the composition compared to the pressure during granulation of the same composition without addition of the block co-polymer.
  • the at least one compound is an agricultural material compound.
  • the agricultural material compound is an agrochemical compound.
  • the agricultural material compound is a pesticide compound.
  • the agricultural material compound is a plant growth regulator, a hormone, or a bio-stimulant.
  • the at least one compound is a non-agricultural material compound.
  • Granulation is a process used for preparing water dispersible granules formulations.
  • some amount of water up to 30% w/w
  • the present block copolymer is added together with this water.
  • the powder is introduced to the granulator.
  • the granulator made of wings rotating at a certain speed (which is determined by the user), pushes the powder through a screen with small holes. In hard cases the powder creates a large pressure that resists this transfer through the screen.
  • the polyelectrolyte layer formed on the particles using the block copolymer improves granulation by remarkably reducing the pressure that develops during the granulation process.
  • the subject invention provides a method of reducing viscosity of a composition comprising at least one compound during milling of the composition by adding an amount of a polyelectrolyte-layer forming block copolymer to the composition, wherein the block copolymer comprises (A) an anchoring moiety and (B) at least one stabilizing moiety, and wherein the amount of block copolymer is effective to reduce the viscosity of the composition during milling of the composition compared to the viscosity of the same composition during milling without addition of the block co-polymer.
  • the subject invention provides a method of reducing temperature during milling of a composition comprising at least one compound by adding an amount of a polyelectrolyte-layer forming block copolymer to the composition, wherein the block copolymer comprises (A) an anchoring moiety and (B) at least one stabilizing moiety, and wherein the amount of block copolymer is effective to reduce the temperature during milling of the composition compared to the temperature during milling of the same composition without addition of the block co-polymer.
  • the at least one compound is an agricultural material compound.
  • the agricultural material compound is an agrochemical compound.
  • the agricultural material compound is a pesticide compound.
  • the agricultural material compound is a plant growth regulator, a hormone, or a bio-stimulant.
  • the at least one compound is a non-agricultural material compound.
  • wet milling is a process used for preparing suspension concentrate formulations.
  • the polyelectrolyte layer formed by the block copolymer significantly lowers/reduces interactions between the particles thereby reducing viscosity and allowing the suspension to be loaded with a high concentration of particles without increasing the temperature of the system.
  • the temperature during milling a 1000 g/L suspension of the present compositions is less than 30° C.
  • the temperature during milling is reduced from 40° C.-50° C. to 20° C.-25° C.
  • the viscosity during milling is reduced from 1000-2000 cPS to 200-400 cPs. Viscosity is measured using the Brookfield viscometer at spindle 62 and 12 RPM.
  • the particle size of 90% of the particle decreases from 50 ⁇ m to 1 ⁇ m as a result of the wet milling process.
  • the present subject matter permits greater density of the formulations and an efficient, low temperature wet milling process.
  • the polyelectrolyte-layer forming block copolymers of the subject invention can function as an adjuvant, and more specifically as a steric dispersant under various conditions in a highly ionic solution.
  • Use of the block copolymers of the subject invention stabilizes, e.g. by prevents or delays settlement of, the particles of compounds in high salt environment.
  • the compound is an agricultural material compound. In one embodiment, the agricultural material compound is an agrochemical compound. In one embodiment, the agricultural material compound is a pesticide compound. In one embodiment, the agricultural material compound is a plant growth regulator, a hormone, or a bio-stimulant. In another embodiment, the compound is a non-agricultural material compound.
  • the subject invention provides a non-agricultural material composition comprising:
  • the subject application provides a colorant system composition comprising:
  • the colorant component may comprise at least one colorant particle and the block co-polymer is adsorbed on a hydrophobic surface of the colorant particle.
  • the dispersant system further comprises a second dispersant.
  • the second dispersant is at least one of a polymeric dispersant, polycarboxylate, sodium polyacrylate, glycol, diethylene glycol, glycerine, C 6-18 alcohol ethoxylate and its sulfate or phosphate, sorbitan monoleate, tristyryl phenol ethoxylate, nopol-containing surfactant or eicosa(propoxy)deca(ethoxy)diethylamine.
  • the colorant composition has a VOC (Volatile Organic Content) of less than about 100 g/L.
  • the colorant composition is compatible with both latex-based coatings and alkyd-based coatings.
  • the subject invention provides a method of tinting an alkyd-based base coating or a latex-based base coating comprising contacting the alkyd-based base coating or the latex-based base coating with a colorant system composition, wherein the colorant system composition comprises:
  • the subject invention also provides an aqueous non-agricultural-application-based composition comprising at least:
  • the aqueous non-agricultural-application-based composition is an emulsion comprising an effective amount of the dispersant system and a film forming polymer latex.
  • the aqueous non-agricultural-application-based composition further comprises one or more of a pigment, a filler, or an extender.
  • the aqueous non-agricultural-application-based composition is an emulsion selected from the group consisting of a latex paint, a latex coating, a cosmetic, a detergent/cleanser, a stimulation fluid and an oilfield drilling fluid.
  • the emulsion is a latex paint.
  • the aqueous non-agricultural-application-based composition further comprises at least one additive selected from the group consisting of surfactants, rheology modifiers, defoamers, thickeners, colorants, waxes, perfumes and co-solvents.
  • the subject invention provides a method of preparing a coating composition comprising contacting a film forming polymer latex with a dispersant system comprising a polyelectrolyte-layer forming block copolymer, wherein the block copolymer comprises (A) an anchoring moiety and (B) at least one stabilizing moiety.
  • the method further comprises contacting the film forming polymer latex with water.
  • the subject invention provides a method of preparing a colorant system composition comprising contacting a colorant component with a dispersant system comprising a polyelectrolyte-layer forming block copolymer wherein the block copolymer comprises (A) an anchoring moiety and (B) at least one stabilizing moiety, and wherein the resulting colorant system composition is a dispersion.
  • the subject invention also provides a polyelectrolyte-layer forming block copolymer for use as an additive in oil cement grout.
  • the polyelectrolyte-layer forming block copolymer is used as a suspending agent in the oil cement grout.
  • the polyelectrolyte-layer forming block copolymer of the invention in combination with the solid particles present in the cement, provides the dispersing effect during the cementing.
  • the subject invention also provides an oil cement grout comprising solid particles and a polyelectrolyte-layer forming block copolymer wherein the block copolymer comprises (A) an anchoring moiety and (B) at least one stabilizing moiety.
  • the subject invention also provides use of a polyelectrolyte-layer forming block copolymer for keeping solid particles in suspension in an oil cement grout, wherein the block copolymer comprises (A) an anchoring moiety and (B) at least one stabilizing moiety.
  • the polyelectrolyte-layer forming block copolymer of the subject invention has one of the structures A, B and C, shown in FIGS. 7, 8 and 9 , respectively.
  • a di-block copolymer is a linear polymer/copolymer and consists of a block of hydrophobic moiety (anchoring moiety) and a block of a hydrophilic charged moiety (stabilizing moiety). (see FIG. 7 )
  • a tri-block copolymer is a linear polymer/copolymer and consists of a hydrophobic moiety and two blocks of hydrophilic charged moiety. (see FIG. 8 )
  • a comb-graft polymer/copolymer consists of a hydrophobic moiety and multiple blocks of a hydrophilic charged moiety, for example 4 blocks of hydrophilic charged moiety as represented in FIG. 9 . This can be referred to simply as a grafted copolymer.
  • the adsorption of the polyelectrolyte-layer forming block copolymer described in the subject invention may be measured by a number of techniques.
  • the polyelectrolyte-layer forming block copolymer of the subject invention may be added to a dispersion of particles in an aqueous medium.
  • the serum may be obtained by centrifuging or filtration of the slurry.
  • the resultant serum could be injected into a size exclusion chromatography device running the relevant method to separate polymer from the matrix and its concentration determined using a calibration curve obtained by injecting polymer samples of known concentration.
  • the centrifuged particles could be washed and their zeta potential measured using equipment known to those skilled in the art.
  • the adsorption of the polyelectrolyte-layer forming block copolymer will result in a net increase of negative charge on the particle surface which corresponds to the formation of a polyelectrolyte brush layer from the adsorbed polymer.
  • the anchoring moiety is a hydrophobic block copolymer. In one embodiment, at least 90% of the anchoring moiety comprises hydrophobic monomers. In some cases, a small amount of hydrophilic monomers (i.e., less than 10% by monomer number) may be introduced to the block.
  • the hydrophobic monomers is selected from the group consisting of acrylate derivatives, methacrylate derivatives, styrene derivatives, and any combination thereof.
  • An alkyl acrylate monomer such as a methyl, ethyl, or butyl acrylate, is one exemplary embodiment in this regard.
  • the hydrophobic monomer is selected from a group consisting of methylacrylate, ethylacrylate, n-propylacrylate, n-butylacrylate, 2-ethyl-hexyl acrylate, methylmethacrylate, ethylmethacrylate, n-propylmethacrylate, n-butylmethacrylate and 2-ethyl-hexyl methacrylate.
  • the hydrophobic monomer is ethyl acrylate.
  • the at least one stabilizing moiety is a hydrophilic block copolymer. In one embodiment, the at least one stabilizing moiety comprises charged monomers. In one embodiment, at least 60% by weight of the stabilizing moiety is charged monomers. In one embodiment, at least 70% by weight of the stabilizing moiety is charged monomers. In one embodiment, at least 80% by weight of the stabilizing moiety is charged monomers. In one embodiment, at least 90% by weight of the stabilizing moiety is charged monomers. In one embodiment, 100% by weight of the stabilizing moiety is charged monomers.
  • the weight percentage of the charged monomers in the stabilizing block is 77% of the weight of the stabilizing block. In another specific embodiment, the weight percentage of the charged monomers in the stabilizing block is 88% of the weight of the stabilizing block. In another specific embodiment, the weight percentage of the charged monomers in the stabilizing block is 68% of the weight of the stabilizing block. In another specific embodiment, the weight percentage of the charged monomers in the stabilizing block is 83% of the weight of the stabilizing block.
  • the weight percentage of the charged monomers of the stabilizing polymer is at least 35% of the total weight of the block copolymer. In another embodiment, the weight percentage of the charged monomers of the stabilizing polymer is 58% of the total weight of the block copolymer.
  • the charged monomers are zwitterionic monomers. In one embodiment, the charged monomers are anionic monomers. In one embodiment, at least 60% of the monomers in the stabilizing block are anionic monomers. In one embodiment, the anionic monomer has a sulfonate group. In one embodiment, the anionic monomer is 2-acrylamido-2-methylpropane sulphonate (AMPS).
  • AMPS 2-acrylamido-2-methylpropane sulphonate
  • the neutral hydrophilic monomer is selected from a group consisting of N-vinylpyrrolidone, ethylene oxide, glycoside acrylate, and acrylamide.
  • the weight percentage of the stabilizing block is 65-90% of the total weight of the block copolymer.
  • the concentration of the block copolymer in the composition is about 0.1%, 0.5%, 1.0%, 1.5%, or 2.0% w/w. In one embodiment, the concentration of the block copolymer in the composition is 0.2-3% w/w.
  • the block copolymer comprises up to 150 monomers. In one embodiment, the block copolymer comprises 85 monomers. In one embodiment, the block copolymer comprises 63 monomers.
  • the weight of the block copolymer is up to about 31000 g/mol. In one embodiment, the weight of the block copolymer is about 17000 g/mol. In another embodiment, the weight of the block copolymer is about 12000 g/mol. In one embodiment, the weight of the block copolymer is 8,000 to 50,000 g/mol. In one embodiment, the weight of the block copolymer is 10,000 to 25,000 g/mol.
  • the weight of the stabilizing block is 5,000 to 100,000 g/mol. In one embodiment, the weight of the stabilizing block is 6,000 to 50,000 g/mol. In one embodiment, the weight of the stabilizing block is 7,000 to 30,000 g/mol.
  • the weight of the anchoring moiety is 500 to 5,000 g/mol. In one embodiment, the weight of the anchoring moiety is 1,000 to 4,000 g/mol.
  • the anchoring moiety comprises alkyl acrylate monomers, preferably ethyl acrylate monomers, and the weight of the anchoring moiety is 1,000 to 4,000 g/mol. In one embodiment, the anchoring moiety comprises alkyl acrylate monomers, preferably ethyl acrylate monomers, and the weight of the anchoring moiety is 1,500 to 3,500 g/mol. In one embodiment, the anchoring moiety comprises alkyl acrylate monomers, preferably ethyl acrylate monomers, and the weight of the anchoring moiety is 1,500 to 3,000 g/mol.
  • the molar ratio of the anchoring moiety to the stabilizing moiety is 1:2-4.
  • the weight ratio between the anchoring moiety and the stabilizing moiety is lower than 0.6, lower than or equal to 0.5, lower than or equal to 0.4, lower than or equal to 0.3, or lower than or equal to 0.2. In one embodiment, the weight ratio between the anchoring moiety and the stabilizing moiety ([anchoring moiety]:[stabilizing moiety]) is between 0.01 and 0.6. In one embodiment, the weight ratio between the anchoring moiety and the stabilizing moiety ([anchoring moiety]:[stabilizing moiety]) is between 0.1 and 0.3.
  • the block copolymer of the subject invention can be synthesized by raft and polymer/copolymerization.
  • the polyelectrolyte-layer forming block copolymer of the invention comprises:
  • living or controlled polymerization as defined by Quirk and Lee (Polymer International 27, 359 (1992)) can be used. This particular method makes it possible to prepare polymers with a narrow dispersity and in which the length and the composition of the blocks are controlled by the stoichiometry and the degree of conversion.
  • copolymers which can be obtained by any so-called living or controlled polymerization method such as, for example:
  • Preferred processes are sequenced living free-radical polymerization processes involving the use of a transfer agent.
  • Preferred transfer agents are agents comprising a group of formula —S—C(S)—Y—, —S—C(S)—S—, or —S—P(S)—Y—, or —S—P(S)—S—, wherein Y is an atom different from sulfur, such as an oxygen atom, a nitrogen atom, and a carbon atom.
  • Y is an atom different from sulfur, such as an oxygen atom, a nitrogen atom, and a carbon atom.
  • They include dithioester groups, thioether-thione groups, dithiocarbamate groups, dithiphosphoroesters, dithiocarbazates, and xanthate groups.
  • groups comprised in preferred transfer agents include groups of formula —S—C(S)—NR—NR′2, —S—C(S)—NR—N ⁇ CR′2, —S—C(S)—O—R, —S—C(S)—CR′CR′2, and —S—C(S)—X, wherein R and R′ are or identical or different hydrogen atoms, or organic groups such as hydrocarbyl groups, optionally substituted, optionally comprising heteroatoms, and X is an halogen atom.
  • a preferred polymerization process is a living radical polymerization using xanthates.
  • Copolymers obtained by a living or controlled free-radical polymerization process may comprise at least one transfer agent group at an end of the polymer chain. In particular embodiment such a group is removed or deactivated.
  • a living or controlled radical polymerization process used to make the block copolymers comprises the steps of:
  • a “living” or “controlled” radical polymerization process used to make the di-block copolymers comprises the steps of:
  • step a a first block of the polymer is synthesized.
  • step b) b1), or b2), another block of the polymer is synthesized.
  • transfer agents are transfer agents of the following formula (I):
  • the R1, R2, R′2 and R3 groups can be substituted by substituted phenyl or alkyl groups, substituted aromatic groups or the following groups: oxo, alkoxycarbonyl or aryloxycarbonyl (—COOR), carboxyl (—COOH), acyloxy (—O2CR), carbamoyl (—CONR2), cyano (—CN), alkylcarbonyl, alkylarylcarbonyl, arylcarbonyl, arylalkylcarbonyl, isocyanato, phthalimido, maleimido, succinimido, amidino, guanidino, hydroxyl (—OH), amino (—NR2), halogen, allyl, epoxy, alkoxy (—OR), S-alkyl, S-aryl or silyl, groups exhibiting a hydrophilic or ionic nature, such as alkaline salts of carboxylic acids or alkaline salts of sulphonic acid, poly(alkylene oxide) (
  • the transfer agent of formula (I) is a dithiocarbonate chosen from the compounds of following formulae (IA), (IB) and (IC):
  • transfer agents are transfer agents of the following formulae (II) and (III):
  • the mono-alpha-ethylenically-unsaturated monomers and their proportions are chosen in order to obtain the desire properties for the block(s). According to this process, if all the successive polymerizations are carried out in the same reactor, it is generally preferable for all the monomers used during one stage to have been consumed before the polymerization of the following stage begins, therefore before the new monomers are introduced. However, it may happen that monomers of the preceding stage are still present in the reactor during the polymerization of the following block. In this case, these monomers generally do not represent more than 5 mol % of all the monomers.
  • the polymerization can be carried out in an aqueous and/or organic solvent medium.
  • the polymerization can also be carried out in a substantially neat melted form (bulk polymerization), or according to a latex type process in an aqueous medium.
  • PolyAgro A is a di-block copolymer, with a total weight of 17000 g/mol, composed of a hydrophobic block (Anchor block—ANCHOR) and a hydrophilic block (Stabilizing block—STAB).
  • the stabilizing, hydrophilic, block is made of sodium 2-Acryloylamino-2-methylpropane-1-sulfonate (AMPS) monomers, which are 77% of the overall monomers in the polymer.
  • AMPS 2-Acryloylamino-2-methylpropane-1-sulfonate
  • the other 23% of the monomers belongs to the anchor, hydrophobic, block which is made of ethyl acrylate monomers.
  • the total amount of monomers in the polymer (degree of polymerization, DPn) is 85 monomers.
  • This polymer may be obtained according to the following procedure.
  • Ethanol was removed from the polymer solution using a rotary evaporator. Water was back added to achieve a polymer solution with a final solids content of 40.4%.
  • the measured solids content was 37.5%.
  • the polymer is used in the formulations according to the below examples from a ready aqua polymer solution at concentration of about 30% w/w.
  • a conventional polymeric dispersant was used (AtloxTM 4913—a non-ionic grafted copolymer).
  • the dispersant system used contains the present di-block copolymer PolyAgro A2 (note: PolyAgro A2 is a water solution with 30% w/w of the PolyAgro A polymer/copolymer of Example 1 as shown above in Table 1). The milling process of the two samples is identical.
  • the active ingredient and the dispersant are introduced into the mixture within three steps, between the steps the mixture is being milled and the viscosity and size distribution of the particles in the mixture is measured, as described in more detail below.
  • Formulation 1 comprising Folpet 1000 g/L as a suspension was prepared by using AtloxTM 4913 as dispersant.
  • Formulation 2 comprising Folpet 1000 g/L as a suspension was prepared by using PolyAgro A2 as dispersant.
  • the active ingredient is added in three steps and so are the dispersants and the wetting agent (Emcol 4500, Sodium dioctyl sulfosuccinate). About half of the Folpet is added immediately, then it is milled, another amount of Folpet is added ( ⁇ 32%) and milled again. On the last step the rest of Folpet is added and milled.
  • the wetting agent Emcol 4500, Sodium dioctyl sulfosuccinate
  • Formulation 1 and Formulation 2 are summarized in Table 2A and 2B below.
  • this graph presents the change in the viscosity between the steps for Formulation 1—without PolyAgro A2, and for Formulation 2—with PolyAgro A2.
  • the viscosity increases, while after milling in each step the viscosity reduces.
  • the viscosity rise is dramatically steeper than in the case of the formulation with the PolyAgro A2.
  • this graph presents the change in the particle side distribution (PSD) during the process (d 90 is a value which 90%, by volume, of the particles has smaller diameter). It shows that the PolyAgro A2 polymer doesn't damage the efficacy of the milling, and that in both cases the reduction in d 90 is similar.
  • High concentration salt solutions with equal amounts of different dispersants were prepared. A dried-milled active ingredient was dispersed in the solution and left for a certain period of time. The sedimentation was then compared between the different solutions.
  • the composition i.e., type of salt, concentrations, dispersants, active ingredient, is specified for each set of measurements in Table 3 below.
  • FIGS. 3A and 3B provides a comparison of performances of different known dispersants and of the PolyAgro A2 dispersant in high salt solutions.
  • active ingredient powder Panrozine
  • high salt concentration ammonium sulfate 10% w/w
  • FIG. 4 provides a further comparison of performances of different known dispersants and of the PolyAgro A2 dispersant in high salt solutions.
  • an equal amount of active ingredient powder (Folpet) was dispersed in different dispersant solutions (1% w/w) with high salt concentration (Sodium chloride 10% w/w). After sitting overnight the only powder remaining dispersed is the one dispersed in the PolyAgro A2 polymer dispersant solution (3 different batches). In the rest of the tubes the powder settled to the bottom.
  • FIGS. 5A and 5B provides another comparison of performances of different known dispersants and of the PolyAgro A2 dispersant in high salt solutions.
  • an equal amount of active ingredient powder Fralpet was dispersed in different dispersant solutions (1% w/w) with high salt concentration ( FIG. 5A —ammonium sulfate 10% w/w; FIG. 5B —Calcium chloride 10.5% w/w).
  • FIG. 5A ammonium sulfate 10% w/w
  • FIG. 5B Calcium chloride 10.5% w/w
  • the only powder remaining dispersed is the one dispersed in the PolyAgro A2 polymer dispersant solution (3 different batches). In the rest of the tubes the powder settled to the bottom.
  • compositions exemplified in the Table 4 were tested for granulation of a Pymetrozin-Dinotefuran formulation.
  • the compositions and granulation process differ only by the surface active agents used.
  • Samples 1 and 2 used conventional surfactants at concentration of 2% while sample 3 used 1% of the PolyAgro A2 polymer solution ( ⁇ 30% w/w).
  • the milled powder was pressed through a screen.
  • the pressure that developed required more electric power to push the powder through the screen.
  • the electric current was measured and was an indication for the pressure. In the case of sample 3, the lowest current was needed in the granulation process indicating the lowest pressure that developed.
  • the formulations without the present block copolymer had a severe pressure problem which developed during granulation, and which was only solved using the present block copolymer.
  • the electrical current needed for the granulator in order to overcome the developed pressure and achieve the necessary granulation speed is given in amperes and indicates the extrusion pressure problem.
  • This is a di-block copolymer, with a total weight of 12000 g/mol, composed of a hydrophobic block (Anchor block—ANCHOR) and a hydrophilic block (Stabilizing block—STAB).
  • the stabilizing, hydrophilic, block is made of sodium 2-Acryloylamino-2-methylpropane-1-sulfonate (AMPS) monomers, which are 69% of the overall monomers in the polymer.
  • AMPS 2-Acryloylamino-2-methylpropane-1-sulfonate
  • the other 31% of the monomers belongs to the anchor, hydrophobic, block which is made of ethyl acrylate monomers.
  • the total amount of monomers in the polymer (degree of polymerization, DPn) is 64 monomers.
  • This polymer may be obtained according to the following procedure.
  • Ethanol was removed from the polymer solution using a rotary evaporator. Water was back added to achieve a polymer solution with a final solids content of 35.8%.
  • the measured solids content were 32.2% (PolyAgro B2).
  • a stable pesticidal formulation of oil in water (o/w) emulsion which is rich in organic phase is presented.
  • the active ingredient is the nematocide Fluensulfone.
  • the composition is presented in Table 7.
  • the organic phase is added to the aqua phase and then the emulsion is produced using high shear homogenizer.
  • the final droplet size is D 90 ⁇ 2 ⁇ m
  • the final Fluensulfone is 630 gr/l
  • the organic phase content is 69%, which is more than twice than the aqua phase.
  • the final viscosity, after high shear is 370 cP (measured at 12 RPM, spindle 62 , Brookfield viscometer.).
  • Example 5 Evaluation of the efficacy and optimum use level of the polymer prepared in Example 5 for the preparation of a pigment color pastes was determined by dispersant demand curve studies. Starting point formulations were chosen for 3 pigments Blue PB 15:2 (40% solids), Black Raven® 5000 (20% solids) and Yellow PY42 (50% solids). For each specific pigment a demand curve was acquired by obtaining 6 viscosity data points corresponding to the dispersion of 6 samples with varying active dispersant to pigment ratios. Each sample contains 1.5 g in total.
  • the amount of dispersant added to each vial was varied such that the active dispersant to pigment ratio was between 6-21% for PB 15:2, 20-70% for Raven® 5000 and 0.3-4% for PY42.
  • the Di water water amount was added such that the final pigment concentrations were 40% for PB 15:2, 20% for Raven® 5000 and 50% for PY42.
  • the mixture was wetted by gentle vortex mixing and then dispersed using vigorous vortex agitation for 90 min using a Scientific industries Vortex-Genie® 2 speed 6-8.
  • the viscosity of the dispersions in the different vials was measured using a Gilson Viscoman portable viscometer.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Dentistry (AREA)
  • Environmental Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Plant Pathology (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Toxicology (AREA)
  • Dispersion Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Ceramic Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Structural Engineering (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Cultivation Of Plants (AREA)
  • Catching Or Destruction (AREA)
  • Manufacturing Of Micro-Capsules (AREA)
  • Graft Or Block Polymers (AREA)
  • Conductive Materials (AREA)
  • Paints Or Removers (AREA)
US15/373,664 2015-12-10 2016-12-09 Polyelectrolyte-layer forming block copolymers and compositions and uses thereof Abandoned US20170172142A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US15/373,664 US20170172142A1 (en) 2015-12-10 2016-12-09 Polyelectrolyte-layer forming block copolymers and compositions and uses thereof
US16/653,595 US11533910B2 (en) 2015-12-10 2019-10-15 Polyelectrolyte-layer forming block copolymers and compositions and uses thereof
US17/946,610 US20230067163A1 (en) 2015-12-10 2022-09-16 Polyelectrolyte-layer forming block copolymers and compositions and uses thereof

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201562265725P 2015-12-10 2015-12-10
US15/373,664 US20170172142A1 (en) 2015-12-10 2016-12-09 Polyelectrolyte-layer forming block copolymers and compositions and uses thereof

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US16/653,595 Continuation US11533910B2 (en) 2015-12-10 2019-10-15 Polyelectrolyte-layer forming block copolymers and compositions and uses thereof

Publications (1)

Publication Number Publication Date
US20170172142A1 true US20170172142A1 (en) 2017-06-22

Family

ID=57960550

Family Applications (3)

Application Number Title Priority Date Filing Date
US15/373,664 Abandoned US20170172142A1 (en) 2015-12-10 2016-12-09 Polyelectrolyte-layer forming block copolymers and compositions and uses thereof
US16/653,595 Active US11533910B2 (en) 2015-12-10 2019-10-15 Polyelectrolyte-layer forming block copolymers and compositions and uses thereof
US17/946,610 Pending US20230067163A1 (en) 2015-12-10 2022-09-16 Polyelectrolyte-layer forming block copolymers and compositions and uses thereof

Family Applications After (2)

Application Number Title Priority Date Filing Date
US16/653,595 Active US11533910B2 (en) 2015-12-10 2019-10-15 Polyelectrolyte-layer forming block copolymers and compositions and uses thereof
US17/946,610 Pending US20230067163A1 (en) 2015-12-10 2022-09-16 Polyelectrolyte-layer forming block copolymers and compositions and uses thereof

Country Status (14)

Country Link
US (3) US20170172142A1 (ja)
EP (1) EP3386299B1 (ja)
JP (1) JP7139246B2 (ja)
CN (1) CN108697074A (ja)
AR (1) AR107038A1 (ja)
AU (2) AU2016367260B9 (ja)
BR (4) BR122022001868B1 (ja)
CA (1) CA3007735A1 (ja)
IL (1) IL259867B (ja)
MA (1) MA43419A (ja)
RU (1) RU2769260C2 (ja)
UA (1) UA123505C2 (ja)
WO (1) WO2017098325A2 (ja)
ZA (1) ZA201803680B (ja)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11597859B2 (en) 2020-01-24 2023-03-07 Oatey Co. Solvent cement formulations having extended shelf life

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20220061314A1 (en) * 2020-08-28 2022-03-03 Grospurt Plant growth regulator in a semisolid or viscous medium
WO2022107098A1 (en) 2020-11-23 2022-05-27 Adama Makhteshim Ltd. Tau-fluvalinate compositions
EP4066638A1 (en) 2021-03-31 2022-10-05 Adama Agan Ltd. Stable emulsions
BR112023019983A2 (pt) 2021-03-31 2023-11-14 Adama Agan Ltd Emulsões estáveis
WO2022264064A1 (en) 2021-06-16 2022-12-22 Adama Makhteshim Ltd. Novaluron water dispersible solid composition
EP4154715A1 (en) 2021-09-24 2023-03-29 Adama Agan Ltd. Agrochemical composition comprising a combination of herbicide active ingredients
AR127776A1 (es) 2021-11-28 2024-02-28 Adama Agan Ltd Composiciones de concentrado en suspensión de alta carga
EP4197327A1 (en) 2021-12-15 2023-06-21 Adama Agan Ltd. Stable suspoemulsions
WO2023126898A1 (en) 2021-12-31 2023-07-06 Adama Makhteshim Ltd. Combination of copper-based fungicide and azole fungicide
TW202410808A (zh) 2022-06-02 2024-03-16 以色列商安道麥馬克西姆有限公司 唑類殺真菌劑組成物
WO2023233380A1 (en) 2022-06-02 2023-12-07 Adama Makhteshim Ltd. Fungicidal compositions
CN117413834A (zh) 2022-07-11 2024-01-19 安道麦马克西姆有限公司 吡蚜酮水性组合物
WO2024018456A1 (en) 2022-07-18 2024-01-25 Adama Makhteshim Ltd. Solid composition of cyantraniliprole and acetamiprid
WO2024028880A1 (en) 2022-08-03 2024-02-08 Adama Makhteshim Ltd. Composition comprising phthalimide fungicide and co-fungicide
WO2024069628A1 (en) 2022-09-29 2024-04-04 Adama Makhteshim Ltd. Concentrated agrochemical compositions of anthranilic diamides

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150189882A1 (en) * 2011-12-15 2015-07-09 Bayer Intellectual Property Gmbh Active ingredient combinations having insecticidal and acaricidal properties
US20160330953A1 (en) * 2013-12-23 2016-11-17 Dow Global Technologies Llc Pymetrozine suspension concentrates and its preparation method

Family Cites Families (73)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4015991A (en) * 1975-08-08 1977-04-05 Calgon Corporation Low fluid loss cementing compositions containing hydrolyzed acrylamide/2-acrylamido-2-methylpropane sulfonic acid derivative copolymers and their use
US4011909A (en) * 1975-09-04 1977-03-15 Calgon Corporation Method of using cementing composition having improved flow properties
US4222881A (en) * 1978-05-01 1980-09-16 Mobil Oil Corporation Oil recovery process involving the injection of thickened water
EP0007731A3 (en) * 1978-07-28 1980-02-20 Imperial Chemical Industries Plc Process for the production of dispersions of hydrophobic particulate solids (e.g. pesticides) and the particulate dispersions thus obtained
US4515635A (en) * 1984-03-23 1985-05-07 Halliburton Company Hydrolytically stable polymers for use in oil field cementing methods and compositions
US5085698A (en) * 1990-04-11 1992-02-04 E. I. Du Pont De Nemours And Company Aqueous pigmented inks for ink jet printers
US5589522A (en) * 1994-12-21 1996-12-31 Lexmark International, Inc. Ink composition
US5763548A (en) 1995-03-31 1998-06-09 Carnegie-Mellon University (Co)polymers and a novel polymerization process based on atom (or group) transfer radical polymerization
DE19621983A1 (de) 1996-06-03 1997-12-04 Basf Ag Verwendung von Copolymeren aus hydrophilen und hydrophoben Monomeren zur Erhöhung der Lösegeschwindigkeit von teilchenförmigen Waschmittelformulierungen in Wasser
KR100479628B1 (ko) 1996-07-10 2005-04-06 이.아이,듀우판드네모아앤드캄파니 리빙 특성을 갖는 중합 방법
US6117921A (en) * 1996-08-30 2000-09-12 E. I. Du Pont De Nemours And Company Process for making printed images using pigmented ink jet compositions
US5708095A (en) * 1996-08-30 1998-01-13 E. I. Du Pont De Nemours And Company Graft copolymers containing sulfonate and phosphonate groups having particular utility as pigmented ink dispersants
FR2764892B1 (fr) 1997-06-23 2000-03-03 Rhodia Chimie Sa Procede de synthese de polymeres a blocs
EP0996643B1 (en) 1997-07-15 2003-03-26 Ciba SC Holding AG Polymerizable compositions containing alkoxyamine compounds derived from nitroso- or nitrone compounds
CA2309279C (en) 1997-12-18 2009-07-14 E.I. Du Pont De Nemours And Company Polymerization process with living characteristics and polymers made therefrom
FR2773161B1 (fr) 1997-12-31 2000-01-21 Rhodia Chimie Sa Procede de synthese de polymeres a blocs
WO1999035177A1 (fr) 1997-12-31 1999-07-15 Rhodia Chimie Procede de synthese de polymeres a blocs par polymerisation radicalaire controlee a partir de composes dithiocarbamates
US6262152B1 (en) * 1998-10-06 2001-07-17 E. I. Du Pont De Nemours And Company Particles dispersed w/polymer dispersant having liquid soluble and cross-linkable insoluble segments
US6204319B1 (en) * 1998-10-30 2001-03-20 E.I. Du Pont De Nemours And Company Aqueous coating compositions
TR200102918T2 (tr) 1999-04-12 2002-01-21 Imperial Chemical Industries Plc Tarım kimyasalı formülasyonları
FR2793634B1 (fr) 1999-05-12 2001-06-29 Schlumberger Systems & Service Dispositif de securisation d'une ligne telephonique dans le domaine audible
FR2794463B1 (fr) 1999-06-04 2005-02-25 Rhodia Chimie Sa Procede de synthese de polymeres par polymerisation radicalaire controlee a l'aide de xanthates halogenes
JP2001019685A (ja) 1999-07-06 2001-01-23 Nippon Bayer Agrochem Co Ltd 殺センチュウ性トリフルオロブテン類
JP2001322988A (ja) 2000-03-09 2001-11-20 Nippon Bayer Agrochem Co Ltd 殺センチュウ性トリフルオロブテン類
DE10034130A1 (de) 2000-07-13 2002-01-24 Bayer Ag Heterocyclische Fluoralkenylthioether (lV)
FR2812293B1 (fr) 2000-07-28 2002-12-27 Rhodia Chimie Sa Procede de synthese de polymeres a blocs par polymerisation radicalaire controlee
AU2001290972A1 (en) 2000-09-14 2002-03-26 Rohm And Haas Company A method for preparing a multi-layered polymeric composite and a multi-layered composite produced thereby
FR2814168B1 (fr) 2000-09-18 2006-11-17 Rhodia Chimie Sa Procede de synthese de polymeres a blocs par polymerisation radicalaire controlee en presence d'un compose disulfure
US6569969B2 (en) 2000-09-28 2003-05-27 Symyx Technologies, Inc. Control agents for living-type free radical polymerization, methods of polymerizing and polymers with same
US6579947B2 (en) 2001-02-20 2003-06-17 Rhodia Chimie Hydraulic fracturing fluid comprising a block copolymer containing at least one water-soluble block and one hydrophobic block
WO2002098409A1 (en) 2001-06-07 2002-12-12 Wyeth Combination therapy for type ii diabetes or syndrome x
ATE426638T1 (de) * 2001-12-12 2009-04-15 Rhodia Chimie Sa Formulierung enthaltend eine anionische verbindung, ein polyionisches polymer und ein copolymer
DE10229776A1 (de) 2002-07-03 2004-01-22 Bayer Cropscience Ag Verfahren zum Herstellen von heterocyclischen Fluoralkenylsulfonen
DE10319590A1 (de) 2003-05-02 2004-11-18 Bayer Cropscience Ag Wirkstoffkombinationen mit nematiziden und insektiziden Eigenschaften basierend auf Trifluorbutenyl-Verbindungen
DE10319591A1 (de) 2003-05-02 2004-11-18 Bayer Cropscience Ag Wirkstoffkombinationen mit nematiziden, insektiziden und fungiziden Eigenschaften basierend auf Trifluorbutenyl-Verbindungen
US20080287294A1 (en) 2005-04-08 2008-11-20 Syngenta Crop Protection, Inc. Method of Mollusc Control
CN102276769B (zh) 2005-04-18 2013-12-04 巴斯夫欧洲公司 一种呈由至少三种不同的单烯属不饱和单体构成的聚合物形式的共聚物
DE102005051823A1 (de) * 2005-10-28 2007-05-03 Basf Ag Polyalkoxylat-haltige feste Pflanzenschutzmittel, Verfahren zu ihrer Herstellung und ihre Verwendung
RU2008132841A (ru) 2006-01-10 2010-02-20 ИННОВАФОРМ ТЕКНОЛОДЖИЗ, ЭлЭлСи (US) Система доставки пестицидов
WO2008004677A1 (fr) 2006-07-07 2008-01-10 Nippon Soda Co., Ltd. Composition antimicrobienne liquide capable de former des films transparents
WO2008036864A2 (en) 2006-09-22 2008-03-27 Huntsman Petrochemical Corporation Ostwald ripening inhibition in chemical formulations
CA2670982A1 (en) 2006-12-13 2008-06-26 Innovaform Technologies, Llc Pesticidal aggregates
JP5114660B2 (ja) 2007-04-23 2013-01-09 東洋紡株式会社 抗血栓性抗菌性組成物および医療用具
KR20110066952A (ko) 2008-09-25 2011-06-17 비브 나노, 인코포레이티드 중합체 나노입자 및 활성 성분의 제형을 제조하는 방법
BRPI0921583A2 (pt) 2008-11-07 2015-08-18 Basf Se Composição, uso de um sistema de solvente, processo para produzir uma composição, uso de uma composição, e, material de semente
TWI508962B (zh) * 2009-04-22 2015-11-21 Du Pont 氮雜環醯胺之固體形態
TW201041509A (en) 2009-04-30 2010-12-01 Dow Agrosciences Llc Pesticide compositions exhibiting enhanced activity
TW201041507A (en) 2009-04-30 2010-12-01 Dow Agrosciences Llc Pesticide compositions exhibiting enhanced activity and methods for preparing same
CA2771006C (en) 2009-08-14 2018-05-01 Bayer Cropscience Ag Aluminium silicate-free, highly concentrated suspension concentrates of metribuzin
US9198424B2 (en) 2010-06-18 2015-12-01 Bayer Intellectual Property Gmbh Active ingredient combinations having insecticidal and acaricidal properties
DE102011014354A1 (de) 2011-03-17 2012-09-20 Clariant International Ltd. Suspensionskonzentrate
GB201111438D0 (en) * 2011-07-04 2011-08-17 Syngenta Ltd Formulation
GB201111439D0 (en) 2011-07-04 2011-08-17 Syngenta Ltd Formulation
WO2013093578A1 (en) * 2011-12-22 2013-06-27 Vive Crop Protection Inc. Strobilurin formulations
CN104053362B (zh) 2012-01-17 2017-04-26 先正达参股股份有限公司 含螺杂环吡咯烷二酮的杀有害生物混合物
EP2836073A1 (en) 2012-03-05 2015-02-18 Ceradis B.V. Polyelectrolyte complexes for biocide enhancement
WO2013186695A1 (en) 2012-06-11 2013-12-19 Vive Crop Protection Inc. Herbicide formulations
JP6189429B2 (ja) 2012-06-22 2017-08-30 ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ ジエチルアミノエチルメタクリレートコポリマーをベースにした活性成分含有固体分散体
FR3011555A1 (fr) * 2013-10-04 2015-04-10 Rhodia Operations Polymeres sequences pour le controle du filtrat
CN103525379A (zh) * 2013-10-21 2014-01-22 中国石油大学(华东) 一种聚合物纳米二氧化硅抗温耐盐降失水剂及其制备方法
WO2015116716A1 (en) 2014-01-29 2015-08-06 Verdesian Life Sciences, Llc Adjuvants for plant growth regulators
EP3193602A1 (en) 2014-09-18 2017-07-26 Adama Makhteshim Ltd Use of heterocyclic fluoroalkenyl sulfone compounds for repelling molluscs
CN104430477A (zh) 2014-11-25 2015-03-25 广东中迅农科股份有限公司 一种含有氟噻虫砜和烟碱类杀虫剂的农药组合物
CN104585224A (zh) 2014-12-27 2015-05-06 江西中迅农化有限公司 一种含有氟噻虫砜和拟除虫菊酯类杀虫剂的农药组合物
CN104585226A (zh) 2014-12-27 2015-05-06 江西中迅农化有限公司 一种含有氟噻虫砜和有机磷类杀虫剂的农药组合物
CN104855392B (zh) 2015-02-04 2016-08-17 东莞市瑞德丰生物科技有限公司 一种杀线虫组合物
CN104982431A (zh) * 2015-06-09 2015-10-21 天津市华宇农药有限公司 一种含有异丙草胺和莠去津的除草剂组合物及其制备方法
CN105165844B (zh) 2015-09-25 2017-10-31 广东真格生物科技有限公司 一种含氟噻虫砜的杀线虫组合物
CN105638689A (zh) 2016-03-03 2016-06-08 陕西上格之路生物科学有限公司 一种含有氟噻虫砜和甲氨基阿维菌素苯甲酸盐的杀线虫组合物
IL267063A (en) 2016-12-09 2019-07-30 Adama Makhteshim Ltd Fluensulfone formulations in high concentration, their uses and processes for their preparation
CA3066200A1 (en) 2017-06-09 2018-12-20 Adama Makhteshim Ltd. Formulation for seed treatment comprising fluensulfone
AR114185A1 (es) 2018-01-23 2020-07-29 Adama Makhteshim Ltd Síntesis de 5-cloro-2-[(3,4,4-trifluoro-3-buten-1-il)tio]-tiazol
BR112020025309A2 (pt) 2018-06-13 2021-03-09 Adama Makhteshim Ltd. Composição estável de amplo espectro, mistura, método para aumentar o desenvolvimento de planta, método para controlar nematoides, método para regular crescimento de planta e método para preparar a composição estável de amplo espectro

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150189882A1 (en) * 2011-12-15 2015-07-09 Bayer Intellectual Property Gmbh Active ingredient combinations having insecticidal and acaricidal properties
US20160330953A1 (en) * 2013-12-23 2016-11-17 Dow Global Technologies Llc Pymetrozine suspension concentrates and its preparation method

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11597859B2 (en) 2020-01-24 2023-03-07 Oatey Co. Solvent cement formulations having extended shelf life
US11976222B2 (en) 2020-01-24 2024-05-07 Oatey Co. Solvent cement formulations having extended shelf life

Also Published As

Publication number Publication date
US20200178521A1 (en) 2020-06-11
BR122022001869B1 (pt) 2022-09-13
CN108697074A (zh) 2018-10-23
EP3386299B1 (en) 2024-04-24
WO2017098325A3 (en) 2017-08-03
AU2016367260B9 (en) 2021-07-29
BR112018011501A2 (pt) 2018-12-04
BR122022001868B1 (pt) 2022-09-13
AU2021203824B2 (en) 2023-07-06
AU2021203824A1 (en) 2021-07-08
IL259867A (en) 2018-07-31
US11533910B2 (en) 2022-12-27
UA123505C2 (uk) 2021-04-14
JP7139246B2 (ja) 2022-09-20
CA3007735A1 (en) 2017-06-15
BR112018011501B1 (pt) 2022-05-31
RU2018124933A3 (ja) 2020-08-28
JP2018538298A (ja) 2018-12-27
AR107038A1 (es) 2018-03-14
AU2016367260A1 (en) 2018-07-19
WO2017098325A4 (en) 2017-11-30
MA43419A (fr) 2018-10-17
RU2018124933A (ru) 2020-01-13
EP3386299A2 (en) 2018-10-17
US20230067163A1 (en) 2023-03-02
AU2016367260B2 (en) 2021-07-08
RU2769260C2 (ru) 2022-03-29
IL259867B (en) 2021-06-30
WO2017098325A2 (en) 2017-06-15
BR122020007824B1 (pt) 2022-05-03
ZA201803680B (en) 2023-01-25

Similar Documents

Publication Publication Date Title
US11533910B2 (en) Polyelectrolyte-layer forming block copolymers and compositions and uses thereof
US11503827B2 (en) Stabilized chemical composition
JP5624188B2 (ja) ピカリング乳剤
KR20080044871A (ko) 수-현탁성 농약 조성물
US20210227823A1 (en) Stabilized chemical composition
CN110099566A (zh) 使用分散组分稳定涂覆有非两性、可季化和水溶性聚合物的颗粒
CN102176822B (zh) 含杀生物剂的高固体分散体
JP6717830B2 (ja) 殺有害生物剤及び共重合性界面活性剤を含有するポリマー粒子の水性分散体
CN117813003A (zh) 农用化学组合物
OA16271A (en) Stabilized chemical composition.

Legal Events

Date Code Title Description
AS Assignment

Owner name: ADAMA MAKHTESHIM, LTD., ISRAEL

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:SILBERT, GILAD;BERKOVITCH, MICHAEL;REEL/FRAME:046745/0643

Effective date: 20161220

Owner name: RHODIA OPERATIONS, FRANCE

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:WILSON, DAVID JAMES;REEL/FRAME:046746/0449

Effective date: 20170113

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STCB Information on status: application discontinuation

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

AS Assignment

Owner name: RHODIA OPERATIONS, FRANCE

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:WILSON, DAVID JAMES;REEL/FRAME:061335/0328

Effective date: 20170113