WO2024033234A1 - Polyester biodégradable utilisé comme dispersant et composition agricole le comprenant - Google Patents

Polyester biodégradable utilisé comme dispersant et composition agricole le comprenant Download PDF

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Publication number
WO2024033234A1
WO2024033234A1 PCT/EP2023/071619 EP2023071619W WO2024033234A1 WO 2024033234 A1 WO2024033234 A1 WO 2024033234A1 EP 2023071619 W EP2023071619 W EP 2023071619W WO 2024033234 A1 WO2024033234 A1 WO 2024033234A1
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Prior art keywords
biodegradable polyester
dispersant
agricultural
polyester used
composition
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PCT/EP2023/071619
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English (en)
Inventor
Ritu Ahuja
Sandeep Thakur
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Specialty Operations France
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Publication of WO2024033234A1 publication Critical patent/WO2024033234A1/fr

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    • 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
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
    • C08G63/688—Polyesters containing atoms other than carbon, hydrogen and oxygen containing sulfur
    • C08G63/6884—Polyesters containing atoms other than carbon, hydrogen and oxygen containing sulfur derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/6886—Dicarboxylic acids and dihydroxy compounds
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/08—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 solids as carriers or diluents
    • A01N25/10—Macromolecular compounds
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
    • 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
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/16—Dicarboxylic acids and dihydroxy compounds
    • C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
    • C08G63/199—Acids or hydroxy compounds containing cycloaliphatic rings
    • 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
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/66—Polyesters containing oxygen in the form of ether groups
    • C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/672—Dicarboxylic acids and dihydroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds

Definitions

  • the present invention provides a biodegradable polyester which can be used as dispersant for agricultural formulations.
  • the present invention further provide an agricultural composition comprising the same.
  • Agricultural compositions are more and more complex with high loading of active ingredients which may be sparingly soluble, or even insoluble, in water, and/or combo systems combining said active ingredients with several modes of action having different physicochemical characteristics: for example, one active can be in the form of a soluble salt and the other one dispersed in an aqueous phase.
  • agricultural compositions typically include dispersants to improve the dispersion, and in particular to provide homogeneity and to help reduce and/or prevent flocculation and agglomeration.
  • Dispersion is the process through which agglomerates of solid particles become separated, and a new interface forms between each of the smaller particles and the surrounding media. This process is facilitated by the application of external force (milling) and the use of amphiphilic additives such as dispersants.
  • biodegradable non-polymeric surfactants such as phosphate esters
  • phosphate esters are not very versatile for many active ingredients and there is a need to utilize polymeric dispersants in order to stabilize the agricultural formulations.
  • Lignosulfonates and EO-POs are biodegradable and can be used as polymeric dispersant, however they are not versatile.
  • biodegradable polyester which can be used as dispersant for agricultural formulations.
  • the biodegradable polyester can be prepared from a monomer composition comprising:
  • SA sulphonated dicarboxylic acid monomer
  • a polyhydric polyol (P) selected from the group consisting of at least one ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol or polyethylene glycol having an ethylene oxide number ranging from 1 to 200, dipropylene glycol, glycerol, 1 ,2,4-butanetriol and 1 ,2,3- butanetriol, and oligomers of thereof having from 1 to 100 monomer units; and
  • a dihydroxyl compound (DH) selected from C 5 - C10 cycloaliphatic diol, C 5 - C cycloaliphatic diacidic acid, C 2 - C 8 hydroxylated aliphatic acid, or the combination thereof.
  • the biodegradable polyester can comprises the following repeating units (I) and (II): wherein Ri, R 2 , R3, and R 4 are independently selected from H or Ci-C 8 alkyl;
  • A is selected from C 5 - C10 cycloaliphatic group or aromatic group; and n and m is a number ranging from 1 to 200.
  • an agricultural composition comprising a pesticide and the biodegradable polyester of the present invention.
  • the agricultural compositions according to the invention reduce, or even prevent, crystal growth of dispersed agricultural material, and also guarantee good performances at dilution including a good suspensibility of the agricultural material, even for high loading formulations.
  • the agricultural compositions according to the invention present a high storage stability over time.
  • the agricultural compositions according to the invention have a good viscosity and a good dispersion of agricultural materials, which allows easier application onto soils, plants and/or seeds.
  • biodegradable polyester of the present invention as dispersant for agricultural compositions.
  • a method for treating soils, plants and/or seeds to control pests and/or to regulate the growth of plants by applying the composition according to the invention to at least one plant, area adjacent to a plant, soil adapted to support growth of a plant, root of a plant, foliage of a plant, and/or seed adapted to produce a plant.
  • any particular upper concentration, weight ratio or amount can be associated with any particular lower concentration, weight ratio or amount, respectively.
  • alkyl means a saturated hydrocarbon radical, which may be straight, branched or cyclic, such as, methyl, ethyl, n-propyl, iso-propyl, n- butyl, sec-butyl, t-butyl, pentyl, n-hexyl, cyclohexyl.
  • (Cn-Cm) in reference to an organic group, wherein n and m are each integers, indicates that the group may contain from n carbon atoms to m carbon atoms per group.
  • the suspensibility of the agricultural composition is defined as the percentage in weight of one or more agricultural material(s) remaining in suspension relative to the total weight of compounds after a given time, after the dilution of said composition at a certain %wt in water (CIPAC A or D standard waters), for example at 1%wt in water.
  • CIPAC A or D standard waters %wt in water
  • good suspensibility is intended to denote a suspensibility greater than or equal to 70%, in particular greater than or equal to 80%, more particularly greater than or equal to 85%, for example greater than or equal to 90%.
  • the suspensibility of a composition can for example be determined according to the CIPAC method MT184.
  • the term “good storage stability” is intended to denote compositions which remain homogeneous (that is to say which exhibit substantially no, or limited, phase separation (sedimentation, syneresis, etc.)) over time, in particular which remain substantially homogeneous when stored for at least one week at 0°C, or for at least 2 weeks at 54°C or at least 3 months at 45°C (CIPAC MT 39.3 and MT 46.3 standardized tests).
  • compositions exhibiting “good flowability” that is to say compositions of suitable viscosity, for example of viscosity greater than 300 cP (i.e. 300 mPa.s), in particular of viscosity greater than 300 cP (i.e. 300 mPa.s) and less than 10,000 cP (i.e. 10,000 mPa.s), measured at 20 rpm and at 25°C using a Brookfield RV viscometer.
  • a shear thinning profile that is to say a viscosity which decreases when the shear rate increases, is generally required, in order to allow good flowability of the composition.
  • a concentrated agricultural composition of the invention must in particular remain pumpable.
  • suitable dispersion or “good dispersion” is intended to mean a dispersion after dilution in water (CIPAC A or D standard waters) which is homogeneous (that is to say which exhibits substantially no phase separation, (sedimentation, syneresis, etc.)) over time, in particular which remains substantially homogeneous when stored for 30 minutes in a water bath thermostatically controlled at 30°C, preferably for 2 hours in a water bath thermostatically controlled at 30°C and ideally for 24 hours in a water bath thermostatically controlled at 30°C (adaptation of the CIPAC MT180 test).
  • CIPAC A or D standard waters water which is homogeneous (that is to say which exhibits substantially no phase separation, (sedimentation, syneresis, etc.)) over time, in particular which remains substantially homogeneous when stored for 30 minutes in a water bath thermostatically controlled at 30°C, preferably for 2 hours in a water bath thermostatically controlled at 30°C and ideally for 24 hours in a water bath thermostat
  • Crystal growth by "Ostwald ripening", generally occurs when smaller crystals (which have a larger surface area than bigger crystals) dissolve in the aqueous phase and the material is transported through the continuous phase, to nucleation sites of bigger crystals.
  • the crystals of the agricultural material may aggregate and sediment, the composition becomes inhomogeneous; during application, filters and nozzles of the spray equipment can block and the biological efficacy may be reduced.
  • the particle size D(50) and D(90) values were determined by dynamic light scattering analysis using a Malvern Mastersizer 2000 with Hydro 2000SM attachments running on deionized water.
  • the particle size D(50) and D(90) values corresponding to the particle diameter such as the cumulative undersized volume fraction of particles is respectively equal to 50 % and to 90%. From the particle size values obtained, D(50) and D(90) values were readily determined.
  • the crystalline morphology of the material was assessed by optical microscopy observation.
  • the sample was diluted to a 5%w/w solution in deionized water, and images of crystalline material taken and processed. In some cases, arbitrary line measurements on the resultant image were used to confirm particle size of the crystals.
  • biodegradable polyester used as dispersant for agricultural compositions.
  • the biodegradable polyester can be prepared from a monomer composition comprising:
  • SA sulphonated dicarboxylic acid monomer
  • a polyhydric polyol (P) selected from the group consisting of at least one ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol or polyethylene glycol having an ethylene oxide number ranging from 1 to 200, dipropylene glycol, glycerol, 1 ,2,4-butanetriol and 1 ,2,3- butanetriol, and oligomers of thereof having from 1 to 100 monomer units; and
  • a dihydroxyl compound (DH) selected from C 5 - C10 cycloaliphatic diol, C 5 - C cycloaliphatic diacidic acid, C 2 - C 8 hydroxylated aliphatic acid, or the combination thereof.
  • the sulphonated dicarboxylic acid monomer has at least one sulphonic acid group, preferably in the form of an alkali metal or alkali earth metal (preferably sodium) sulphonate, and two acidic functional groups or acidic functional group equivalents (that is to say an anhydride functional group or two ester functional groups) attached to one or a number of aromatic rings, when aromatic dicarboxylic acids or anhydrides or their diesters are involved, or to the aliphatic chain when aliphatic dicarboxylic acids or anhydrides or their alkyl diesters are involved.
  • SA sulphonated dicarboxylic acid monomer
  • SA sulphonated dicarboxylic acid monomers
  • aromatic sulphonated dicarboxylic acids or anhydrides such as sulphoisophthalic, sulphoterephthalic, sulpho-ortho-phthalic acids or anhydrides, 4-sulpho-2,7-naphthalenedicarboxylic acids or anhydrides, sulpho-4,4’- bis(hydroxycarbonyl)diphenyl sulphones, sulphodiphenyldicarboxylic acids or anhydrides, sulpho-4,4’-bis(hydroxycarbonyl)diphenylmethanes, sulpho-5- phenoxyisophthalic acids or anhydrides or their lower (methyl, ethyl, propyl, isopropyl, butyl) diesters and sulphonated aliphatic sulphonated dicarboxylic acids or anhydrides such as sulphosuccinic
  • the sulphonated dicarboxylic acid monomers are selected from aromatic sulphonated dicarboxylic acids, preferably sulphoisophthalic, sulphoterephthalic, sulpho-ortho-phthalic acids or anhydrides lower diesters thereof.
  • the polyhydric polyol (P) used in the present invention is at least one polyol selected from the group consisting of ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol or polyethylene glycol having an ethylene oxide number ranging from 1 to 200, dipropylene glycol, glycerol, 1 ,2,4- butanetriol and 1 ,2,3-butanetriol, and oligomers of thereof having from 1 to 100 monomer units; preferably used is ethylene glycol and/or glycerol.
  • the dihydroxyl compound (DH) used in the present invention is selected from C 5 - C10 cycloaliphatic diol, C 5 - C10 cycloaliphatic diacidic acid, C 2 - C 8 hydroxylated aliphatic acid, or the combination thereof.
  • the illustrative example of C 5 - C10 cycloaliphatic diol include but not limited to cyclohexane dimethanol
  • the illustrative example of C 2 - C 8 hydroxylated aliphatic acid include but not limited to glycolic acid
  • the illustrative example of C 5 - C10 cycloaliphatic diacidic acid monomer include but not limited to cyclohexane dicarboxylic acid.
  • more than one dihydroxyl compounds can be used, for example, cyclohexane dimethanol and cyclohexane dicarboxylic acid can be used together in the present invention.
  • the dihydroxyl compound(s) is used in an amount of 0.1% to 50 %, preferably between 0.5% to 25%, more preferably between 0.5% to 15%, based on the 100 molar % of the biodegradable polyester.
  • the monomer composition for preparing the polyester further comprises:
  • a diacidic component which is at least one selected from d1) an unsulphonated dicarboxylic acid monomer (A) consisting of at least one dicarboxylic acid or derivatives thereof selected from the group consisting of terephthalic, isophthalic, 2,6-naphthalenedicarboxylic acids and furan dicarboxylic acid; and d2) a polyester prepolymer prepared from the unsulphonated dicarboxylic acid monomers (A) or derivatives thereof and the polyhydric polyol (P).
  • A unsulphonated dicarboxylic acid monomer
  • P polyhydric polyol
  • the unsulphonated dicarboxylic acid monomerdicarboxylic acid monomers (A) are consisted of isophthalic and/or furan dicarboxylic acids.
  • the unsulphonated dicarboxylic acid monomer (A) there may additionally be present minor quantities of aromatic diacids other than those mentioned above, such as orthophthalic acid, anthracene, 1 ,8-naphthalene, 1 ,4-naphthalene and biphenyl dicarboxylic acids or aliphatic diacids such as adipic, glutaric, succinic, trimethyladipic, pimelic, azelaic, sebacic, suberic, itaconic and maleic acids, etc. in the form of acid, anhydride or lower (methyl, ethyl, propyl, isopropyl, butyl) diesters.
  • aromatic diacids other than those mentioned above, such as orthophthalic acid, anthracene, 1 ,8-naphthalene, 1 ,4-naphthalene and biphenyl dicarboxylic acids or aliphatic diacids such as adipic, glutaric
  • the prepolymer c2) used in the present invention is prepared from the unsulphonated dicarboxylic acid monomerdicarboxylic acid monomers (A) or the derivatives thereof and the polyhydric polyol (P).
  • the prepolymer c2) is polyethylene terephthalate which can be prepared from terephthalic acid, isophthalic acid, ethylene glycol and/or diethylene glycol.
  • the prepolymer c2) has an intrinsic viscosity range between 0.1 to 0.9 dL/g determined according to ASTM method D-4603 and has a maximum melting point of 250 °C.
  • biodegradable polyester used as dispersant of the present invention can be prepared by the process of esterification or transesterification and polycondensation according to the common knowledge in the art. US 09/887664 discloses such a process of preparing the water-dispersible polyester polymer, which are hereby incorporated herein by reference in their entirety.
  • biodegradable polyester comprises the following repeating units (I) and (II): wherein R1, R 2 , R3, and R 4 are independently selected from H or Ci-C 8 alkyl;
  • A is selected from C 5 - C10 cycloaliphatic group or aromatic group; and n and m is a number ranging from 1 to 200.
  • one of R1 and R 2 is selected from H, the other is selected from H, methyl, ethyl, propyl, or butyl, preferably methyl.
  • the biodegradable polyester further comprises the repeating units (III) wherein R 5 and R 6 are independently selected from H or Ci-C 8 alkyl; and p is a number ranging from 1 to 200.
  • one of R 5 and R 6 is selected from H, the other is selected from H, methyl, ethyl, propyl, or butyl, preferably methyl.
  • the biodegradable polyester further comprises at least one of the repeating units IV to VI, wherein A is defined as above, B is selected from C 5 - C10 cycloaliphatic group.
  • B is represented hexamethylenyl.
  • A is selected from hexamethylenyl.
  • an agricultural composition comprising:
  • the agricultural composition according to the invention comprises at least one agricultural material.
  • the term “agricultural material” means an active ingredient used in the practice of farming, including cultivation of the soil for the growing of 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.
  • the agricultural material(s) are chosen from pesticides, antimicrobials, nutrients, biostimulants, plant growth regulators, and mixtures thereof.
  • pesticides include fungicides, herbicides, insecticides, algicides, moluscicides, miticides, nematicides, and rodenticides.
  • antimicrobials include germicides, antibiotics, antibacterials, antivirals, antifungals, antiprotozoals, antiparasites.
  • the agricultural material(s) are selected from fungicides, herbicides, insecticides, algicides, moluscicides, miticides, nematicides, rodenticides, germicides, antibiotics, antibacterials, antivirals, antifungals, antiprotozoals, antiparasites, and mixtures thereof.
  • Suitable pesticides, antimicrobials, plant growth regulators, nutrients and biostimulants for use in the composition according to the invention may be chosen from those cited in the international application WO 2019/185851 from CRODA.
  • Pesticide' will be understood to refer to any substance or mixture of substances intended for preventing, destroying, repelling, or mitigating any pest.
  • a pesticide may be a chemical substance, a biological agent (such as a macroorganisms, a microorganisms), a semiochemicals (such as pheromone) or natural substances of mineral, plant or animal origin used against pests including insects, plant pathogens, weeds, mollusks, birds, mammals, fish, nematodes (roundworms) and microbes that compete with humans for food, destroy property, spread disease or are a nuisance.
  • Pesticides includes biopesticides. The skilled worker is familiar with such pesticides, which can be found, for example, in the Pesticide Manual, 16th Ed. (2013), The British Crop Protection Council, London. In the following examples, pesticides suitable for the agricultural compositions according to the present invention are given.
  • the pesticides are chosen from insecticides, fungicides, herbicides, miticides, and mixtures thereof.
  • a fungicide refers to any substance or mixture of substances used to prevent the spread of fungi in gardens and crops. Fungicides are also used to fight fungal infections. Fungicides can either be contact or systemic. A contact fungicide kills fungi when it comes into contact with the fungicide retained on leaf surfaces. A systemic fungicide is absorbed into plant tissues and kills the fungus when it attempts to invade the host.
  • fungicides examples include, but are not limited to: (3-ethoxypropyl)-mercury bromide, 2-methoxyethylmercury chloride, 2-phenylphenol, 8-hydroxyquinoline sulfate, 8- phenylmercurioxyquinoline, acibenzolar, acibenzolar-S-methyl, acypetacs, acypetacs-copper, acypetacs-zinc, aldimorph, allyl alcohol, ametoctradin, amisulbrom, ampropylfos, anilazine, aureofungin, azaconazole, azithiram, azoxystrobin, barium polysulfide, benalaxyl, benalaxyl-M, benodanil, benomyl, benquinox, bentaluron, benthiavalicarb, benthiavalicarb-isopropy
  • An herbicide is a pesticide used to kill unwanted plants. Selective herbicides kill specific targets while leaving the desired crop relatively unharmed. Some of these act by interfering with the growth of the weed and are often based on plant hormones. Herbicides used to clear waste ground are non-selective and kill all plant material with which they come into contact. Herbicides are widely used in agriculture and in landscape turf management. They are applied in total vegetation control (TVC) programs for maintenance of highways and railroads. Smaller quantities are used in forestry, pasture systems, and management of areas set aside as wildlife habitat.
  • TVC total vegetation control
  • herbicides examples include, but are not limited to: 4-CPA, 4-CPB, 4-CPP, 2,4-D, 3,4- DA, 2,4-DB, 3,4-DB, 2,4- DEB, 2,4-DEP, 3,4-DP, 2,3,6-TBA, 2,4,5-T, 2,4,5-TB, acetochlor, acifluorfen, aclonifen, acrolein, alachlor, allidochlor, alloxydim, allyl alcohol, alorac, ametridione, ametryn, amibuzin, amicarbazone, amidosulfuron, aminocyclopyrachlor, aminopyralid, amiprofos-methyl, amitrole, ammonium sulfamate, anilofos, anisuron, asulam, atraton, atrazine, azafenidin, azimsulfuron, aziprotryne, barban, BCPC, beflu
  • Safeners mean active ingredients applied with herbicides to protect crops against their injury.
  • Some of the safeners that can be employed in the present disclosure include, but are not limited to: benoxacor, benthiocarb, brassinolide, cloquintocet (mexyl), cyometrinil, daimuron, dichlormid, dicyclonon, dimepiperate, disulfoton, fenchlorazole-ethyl, fenclorim, flurazole, fluxofenim, furilazole, isoxadifen-ethyl, mefenpyr-diethyl, MG 191 , MON 4660, naphthalic anhydride (NA), oxabetrinil, R29148, N-phenylsulfonylbenzoic acid amides and mixtures thereof.
  • benoxacor benthiocarb
  • brassinolide cloquintocet (mexyl)
  • An insecticide is a pesticide used against insects in all developmental forms, and include ovicides and larvicides used against the eggs and larvae of insects. Insecticides are used in agriculture, medicine, industry and the household.
  • insecticides examples include, but are not limited to: 1 ,2- dichloropropane, abamectin, acephate, acetamiprid, acethion, acetoprole, acrinathrin, acrylonitrile, alanycarb, aldicarb, aldoxycarb, aldrin, allethrin, allosamidin, allyxycarb, alpha-cypermethrin, alpha-ecdysone, alpha-endosulfan, amidithion, aminocarb, amiton, amiton oxalate, amitraz, anabasine, athidathion, azadirachtin, azamethiphos, azinphos-ethyl, azinphos- methyl, azothoate, barium hexafluoro silicate, barthrin, bendiocarb, benfuracarb,
  • Miticides are pesticides that kill mites.
  • Antibiotic miticides, carbamate miticides, formamidine miticides, mite growth regulators, organochlorine, permethrin and organophosphate miticides all belong to this category.
  • Molluscicides are pesticides used to control mollusks, such as moths, slugs and snails. These substances include metaldehyde, methiocarb and aluminium sulphate.
  • a nematicide is a type of chemical pesticide used to kill parasitic nematodes (a phylum of worm).
  • the amount of pesticide(s) in the composition ranges from 1 to 95 % by weight, relative to the total weight of the composition.
  • the amount of antimicrobial(s) in the composition ranges from 1 to 95 % by weight, relative to the total weight of the composition.
  • the sum of the amount of antimicrobial(s) and of the amount of pesticide(s) in the composition ranges from 1 to 95 % by weight, relative to the total weight of the composition
  • composition according to the invention may comprise at least one biopesticide.
  • biopesticide includes microorganisms that control pests (microbial pesticides), macroorganisms that control pests, semiochemicals that control pests and natural substance of mineral, plant or animal origin that control pests.
  • Microbial pesticides means any microorganism, whether in a vegetative state, a dormant state (e.g., spore) or a whole broth culture, any substance derived from a microorganism (e.g., metabolites), or any fermentation product (e.g., supernatants, filtrates, extracts, etc.) that are pathogenic to a pest (e.g., capable of attacking, infecting, killing, disabling, causing disease, compete with and/or causing injury to a pest), and is thus able to be used in the control of a pest by adversely affecting the viability or growth of the target pest.
  • microbial pesticides include microbial nematocides, microbial insecticides, microbial fungicides, microbial bactericides, and microbial viricides).
  • the biopesticide are chosen from fungal spores and/or bacterial spores.
  • Examples of fungal spores or conidia that are insecticidal or nematicidal or fungicidal include but not limited to the following classes: Basidiomycetes, Chytridiomycetes, Deuteromycetes, Hyphochytridiomycetes, Oomycetes, Plasmodiophoromycetes, Sordahomycetes, Thchomycetes and Zygomycetes, specifically the following fungi; Arthrobotrys superba, Arthrobotrys irregular, Beauveria bassiana, Erynia neoaphidis, Fusarium spp., Hirsute/ la rhossiliensis, Hirsutella thompsonii, Lagenidium giganteum, Metarhiziurn anisopliae, Myrothecium, Neozygietes fresenii (Nowakowski), Nomuraea rileyi, Paecilomyces lilac
  • bacterial spores include but not limited to Bacillus agri, Bacillus aizawai, Bacillus albolactis, Bacillus amyloliquefaciens, Bacillus cereus, Bacillus circulans, Bacillus coagulans, Bacillus endoparasiticus, Bacillus endorhythmos, Bacillus firmus, Bacillus kurstaki, Bacillus lacticola, Bacillus lactimorbus, Bacillus lactis, Bacillus laterosporus, Bacillus lentimorbus, Bacillus licheniformis, Bacillus macerans, Bacillus megatehum, Bacillus medusa, Bacillus metiens, Bacillus natto, Bacillus nigricans, Bacillus popillae, Bacillus pumiliss, Bacillus pumilus, Bacillus siamensis, Bacillus sphaehcus, Bacillus spp., Bacillus
  • Photorhabdus luminescens Xenorhabdus nematophilus
  • pantoea agglomerans those nematicidal bacterial antagonists listed in "Nematology Advances and Perspectives, Vol. 2 (2004)”.
  • the amount of biopesticide(s) in the composition ranges from 1 to 95 % by weight, relative to the total weight of the composition.
  • composition according to the invention may comprise at least one nutrient.
  • Nutrients refer to chemical elements and compounds which are desired or necessary to promote or improve plant growth. Nutrients generally are described as macronutrients or micronutrients.
  • Suitable nutrients for use in the compositions according to the invention may be micronutrient compounds, preferably those which are solid at room temperature (25°C) or are partially soluble.
  • Micronutrients typically refer to trace metals or trace elements, and are often applied in lower doses. Suitable micronutrients include trace elements selected from zinc, boron, chlorine, copper, iron, molybdenum, and manganese.
  • the micronutrients may be in a soluble form or included as insoluble solids, and may in the form of salts or chelates.
  • the micronutrient is in the form of a carbonate or oxide.
  • the micronutrients may be selected from zinc, calcium, molybdenum or manganese, or magnesium. More preferentially micronutrients for use in the compositions according to the invention may be selected from zinc oxide, manganese carbonate, manganese oxide, or calcium carbonate.
  • composition according to the present invention may also comprise at least one macronutrient.
  • Micronutrients typically refer to those comprising nitrogen, phosphorus, and potassium, and include fertilisers such as ammonium sulphate, and water conditioning agents. Suitable macronutrients include fertilisers and other nitrogen, phosphorus, or sulphur containing compounds, and water conditioning agents.
  • Suitable fertilisers include inorganic fertilisers that provide nutrients such as nitrogen, phosphorus, potassium or sulphur. Examples of such fertilisers include:
  • nitrates and or ammonium salts such as ammonium nitrate, including in combination with urea e.g. as uran type materials, calcium ammonium nitrate, ammonium sulphate nitrate, ammonium phosphates, particularly mono-ammonium phosphate, diammonium phosphate and ammonium polyphosphate, ammonium sulphate, and the less commonly used calcium nitrate, sodium nitrate, potassium nitrate and ammonium chloride;
  • urea e.g. as uran type materials, calcium ammonium nitrate, ammonium sulphate nitrate, ammonium phosphates, particularly mono-ammonium phosphate, diammonium phosphate and ammonium polyphosphate, ammonium sulphate, and the less commonly used calcium nitrate, sodium nitrate, potassium nitrate and ammonium chloride;
  • - for phosphorus as the nutrient acidic forms of phosphorus such as phosphoric, pyrophosphoric or polyphosphoric acids, but more usually salt forms such as ammonium phosphates, particularly mono-ammonium phosphate, di-ammonium phosphate, and ammonium polyphosphate, potassium phosphates, particularly potassium dihydrogen phosphate and potassium polyphosphate; - for sulphur as the nutrient: ammonium sulphate and potassium sulphate, e.g. the mixed sulphate with magnesium.
  • the amount of nutrient(s) in the composition range from 1 to 40 % by weight, more preferentially from 10 to 35 % by weight; even more preferentially from 15 to 30 % by weight, relative to the total weight of the composition.
  • the amount of micronutrient(s) in the composition range from 1 to 40 % by weight, more preferentially from 10 to 35 % by weight; even more preferentially from 15 to 30 % by weight, relative to the total weight of the composition.
  • the amount of macronutrient(s) in the composition range from 1 to 40 % by weight, more preferentially from 10 to 35 % by weight; even more preferentially from 15 to 30 % by weight, relative to the total weight of the composition.
  • biostimulant is intended to mean a compound which may enhance metabolic or physiological processes such as respiration, photosynthesis, nucleic acid uptake, ion uptake, nutrient delivery, or a combination thereof.
  • biostimulants include seaweed extracts (e.g., ascophyllum nodosum), humic acids (e.g., potassium humate), fulvic acids, myoinositol, glycine, and combinations thereof.
  • seaweed extracts e.g., ascophyllum nodosum
  • humic acids e.g., potassium humate
  • fulvic acids e.g., myoinositol, glycine, and combinations thereof.
  • the amount of biostimulant(s) in the composition range from 0.001 to 10 % by weight, more preferentially from 0.01 to 5 % by weight; even more preferentially from 0.1 to 1 % by weight, relative to the total weight of the composition.
  • composition according to the invention may comprise at least one plant growth regulator.
  • Plant growth regulators mean active ingredients used to influence the growth characteristics of plants.
  • plant growth regulators which may be used in the present disclosure include, but are not limited to: 1 -naphthaleneacetic acid, 1 -naphthaleneacetic acid -salt, 1-napthol, 2,4-dichlorophenoxyacetic acid (2,4-D), 2,4-DB, 2,4-DEP, 2,3,5-triiodobenzoic acid, 2,4,5-trichlorophenoxyacetic acid, 2- naphthoxyacetic acid, 2-naphthoxyacetic acid sodium salt, 3-chloro-4- hydroxyphenylacetic acid, 3-indoleacetic acid, 4-biphenylacetic acid, 4- chlorophenoxyacetic acid (4-CPA), 4-hydroxyphenylacetic acid, 6- benzylaminopurine, auxindole, a-naphthaleneacetic acid K-salt, B- naphfhoxyacetic acid, p-chloroph
  • the amount of plant growth regulator(s) in the composition ranges from 1 to 95 % by weight, relative to the total weight of the composition.
  • the agricultural composition according to the invention is aqueous.
  • the water content of the composition ranges from 5% to 99% by weight, more preferentially from 20% to 98% by weight, even more preferentially from 25% to 97% by weight, relative to the total weight of the composition.
  • the pH of the agricultural composition ranges from 1 to 11 ; more preferentially from 3 to 9; and even better from 4 to 8.
  • the pH of the agricultural compositions can be adjusted to the desired value by means of basifying agents or acidifying agents.
  • Use may be made, among the basifying agents, of one or more alkaline agents, such as ammonia, sodium hydroxide or ethanolamine.
  • Mention may be made, by way of examples, among the acidifying agents, of inorganic or organic acids, such as hydrochloric acid or orthophosphoric acid.
  • the agricultural composition according to the invention may further contains additives different from the ingredients described previously, such as binders, diluents, absorbents, dispersants different from those described previously, carriers, disintegration agents, wetting agents, emulsifiers, antifoam agents, antifreeze agents, solvents, viscosity modifiers, preservatives and/or antimicrobials.
  • additives different from the ingredients described previously such as binders, diluents, absorbents, dispersants different from those described previously, carriers, disintegration agents, wetting agents, emulsifiers, antifoam agents, antifreeze agents, solvents, viscosity modifiers, preservatives and/or antimicrobials.
  • Each additive can be present in the agricultural composition according to the invention in an amount ranging from 0% to 20% by weight, more preferably from 0% to 10% by weight, relative to the total weight of the composition.
  • the viscosity of an aqueous agricultural composition according to the invention ranges from 500 mPa.s to 1 500 mPa.s; more preferentially from 700 to 1 300 mPa.s.
  • the agricultural composition according to the invention may be in the form of a concentrate of agricultural material(s), a diluted concentrate, or a sprayable diluted.
  • the agricultural composition according to the invention may be in the form of an emulsifiable concentrate (EC), emulsion in water concentrate (EW), suspension concentrate (SC), capsule suspension (CS), ZC formulation, flowable concentrate for seed treatment (FS), water dispersible granules (WDG) and/or suspoemulsions (SE).
  • EC emulsifiable concentrate
  • EW emulsion in water concentrate
  • SC suspension concentrate
  • CS capsule suspension
  • ZC formulation ZC formulation
  • flowable concentrate for seed treatment FS
  • WDG water dispersible granules
  • SE suspoemulsions
  • the agricultural composition according to the invention is formulated as a suspension concentrate (SC), a flowable concentrate for seed treatment (FS) or a suspoemulsions (SE).
  • SC suspension concentrate
  • FS flowable concentrate for seed treatment
  • SE suspoemulsions
  • the agricultural composition is an aqueous suspension having a concentration of greater than 0.05 g/L of agricultural material(s).
  • the agricultural composition is an aqueous suspension having a concentration of between 0.05 g/L to 1 200 g/L of agricultural material(s).
  • the agricultural composition is a concentrated aqueous suspension having a concentration of greater than 50 g/L of agricultural material(s).
  • the agricultural composition is a concentrated aqueous suspension having a concentration of between 50 g/L to 1 200 g/L of agricultural material(s), even more preferentially between 400 g/L to 1 200 g/L, for instance higher than 700 g/L.
  • the concentrated agricultural composition may be diluted in water for use resulting in a dilute composition having a concentration of greater than 0.05 g/L of agricultural material(s).
  • the concentrated agricultural composition may be diluted in water for use resulting in a dilute composition having a concentration of between 0.05 g/L to 120 g/L of agricultural material(s), even more preferentially between 0.4 g/L to 120 g/L, for instance higher than 0.7 g/L.
  • the copolymer according to the invention may also reduce the viscosity of the agricultural composition during milling of the composition compared to the viscosity of the same agricultural composition during milling without addition of the copolymer according to the invention.
  • the copolymer according to the invention may also reduce the temperature during milling of the agricultural composition compared to the temperature during milling of the same agricultural composition during milling without addition of the copolymer according to the invention.
  • the copolymer layer formed on the particles by the copolymer according to the invention may lower/reduce 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 present copolymer according to the invention permits greater density of the formulations and an efficient, low temperature wet milling, process.
  • the agricultural composition according to the invention is formulated as water dispersible granules (WDG).
  • the granules can include solid support, filler or diluent material(s) which is desirably inert to the agricultural material(s), but which is readily dispersible in water, if necessary in conjunction with dispersing agents. These materials may also have the benefit of reducing granule dry clumping and the disintegration rate (on addition to water) and can also be used to adjust the agricultural material(s) concentration(s).
  • Examples include clays such as kaolin (china clay) and bentonite clays, which may be natural bentonites or modified e.g. activated bentonites, synthetic and diatomaceous silicas, calcium and magnesium silicates, titanium dioxide, aluminium, calcium or magnesium carbonate, ammonium, sodium, potassium, calcium or barium sulphate, charcoal, starch, including modified starches such as alkyl and carboxyalkyl starches, cellulose, such as microcrystalline cellulose, and cellulose derivatives such as carboxyalkyl cellulose, and mixtures of two or more such solid support, filler, diluent materials.
  • clays such as kaolin (china clay) and bentonite clays, which may be natural bentonites or modified e.g. activated bentonites, synthetic and diatomaceous silicas, calcium and magnesium silicates, titanium dioxide, aluminium, calcium or magnesium carbonate, ammonium, sodium, potassium, calcium or barium sulphate, charcoal, starch, including modified starches
  • the copolymer according to the invention facilitates the disintegration of the granules after the addition of water to form a homogeneous dispersion and guarantee good performances at dilution including a good suspensibility of the active ingredients, and lead to low residues, when passing the diluted formulation through a sieve of mesh size of 200.
  • the suspensibility performances can be evaluated with the CIPAC method MT184 after a dilution at 0.5% or 1.0% in CIPAC standard waters A, D or C. In the present application, the suspensibility performances was evaluated with the CIPAC method MT184 after a dilution at 1.0% in CIPAC standard waters C.
  • the easiness of disintegration of the granules to form a dispersion is evaluated after a dilution at 1% in CIPAC standard water D in a measuring cylinder.
  • the number of inversions of the measuring cylinder to disintegrate completely the granules and to form a suspension is assessed, with an acceptance criteria to be below than 30 inversions.
  • the copolymer according to the invention significantly reduces the amount of non-dispersible material obtained after dilution of the WDG formulation.
  • the amount of non- dispersible material can be evaluated with the CIPAC method MT185 (wet sieve test). A sample of the formulation is dispersed in water and the suspension formed is transferred to a sieve, for example of 200 mesh size, and washed. The amount of the material retained on the sieve is determined by drying and weighing.
  • the copolymer according to the invention may reduce the pressure during the possible granulation of the agricultural composition compared to the pressure during granulation of the same agricultural composition without addition of the copolymer according to the invention.
  • Granulation is a process used for preparing water dispersible granules formulations.
  • some amount of water up to 30% w/w
  • the copolymer according to the invention 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 copolymer layer formed on the particles using the copolymer according to the invention may improve granulation by remarkably reducing the pressure that develops during the granulation process.
  • the invention relates to the use of the agrochemical composition as described previously, for the treatment of soils, plants and/or seeds to control pests and/or to regulate the growth of plants.
  • the invention also relates to a method for treating soils, plants and/or seeds to control pests and/or to regulate the growth of plants, by applying the composition according to the invention as described previously to at least one plant, area adjacent to a plant, soil adapted to support growth of a plant, root of a plant, foliage of a plant, and/or seed adapted to produce a plant.
  • composition according to the invention may kill or inhibit pests and/or clean and/or inhibit growth of undesired plants.
  • the agrochemical composition according to the invention can be diluted and applied to at least one plant, area adjacent to a plant, soil adapted to support growth of a plant, root of a plant, foliage of a plant, and/or seed adapted to produce a plant, in a customary manner; for example by watering (drenching), drip irrigation, spraying, and/or atomizing.
  • biodegradable polyesters were prepared by the process below:
  • a stainless steel reactor equipped with an overhead stirrer, nitrogen inlet, condenser setup with receiving vessel and a solid addition port was charged with 384.2g (2.209mol) of 1 ,4 cyclohexanedicarboxylic acid, 155.9g (0.552 mol) of 5-Sulfoisophthalic acid sodium salt, 3.49g (0.011 mmol) of Titanium(IV) (triethanolaminato)isopropoxide solution (80 wt. % in isopropanol) [Tyzor TE] and 519.4 g (8.28 mol) of Ethylene Glycol.
  • the mixture was heated to 160 °C under nitrogen blanket and the reaction mixture was maintained at the same temperature for 60 minutes under agitation, then the reaction temperature was raised to 200 °C and gradually a reduced pressure of WOmBarwas achieved, under this condition ethylene glycol started distilling and was collected in a receiver.
  • the reaction temperature was then increased to 235 °C under reduced pressure. As the reaction achieved 235 °C the pressure was further reduced to 20 mBar.
  • the reaction was maintained for 60 minutes in this condition after which the temperature was decreased to stop the polymerization. Polymer was discharged after it reached room temperature
  • the biodegradability test is done according inherent biodegradability test with OECD 302B.
  • biodegradability test result is over 70% calculated based on the theoretical oxygen demand or ThOD and fulfilled the validity criteria of the test, it will be deemed as passing the readily biodegradability test.
  • Imidaclorid 48% SC of the present invention were prepared as following:
  • the Diuron 80% WDG of the present invention were prepared as following:
  • the Imidacloprid 70% WDG of the present invention were prepared as following:
  • Atrazine 87% WDG of the present invention were prepared as following:
  • Table 5 shows the dispersant of the present invention can also be used in WDG formulation, and endows favorable suspensibility to the WDG formulation comprising the same.

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Abstract

La présente invention concerne un polyester biodégradable qui peut être utilisé en tant que dispersant dans des formulations agricoles. De plus, la présente invention concerne également une composition agricole le comprenant.
PCT/EP2023/071619 2022-08-08 2023-08-03 Polyester biodégradable utilisé comme dispersant et composition agricole le comprenant WO2024033234A1 (fr)

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Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4427557A (en) * 1981-05-14 1984-01-24 Ici Americas Inc. Anionic textile treating compositions
US5019389A (en) 1988-10-13 1991-05-28 University Of Arkansas Method of controlling crop and plant pests
US6168947B1 (en) 1999-02-11 2001-01-02 Food Industry Research And Development Institute Nematophagous fungus Esteya vermicola
EP0763068B1 (fr) * 1994-05-30 2001-09-05 Rhodia Chimie Compositions detergentes comprenant des polyesters sulfones
US9887664B2 (en) 2015-03-04 2018-02-06 David Lawrence Hammers Solar panel module with increased volume of solar production
WO2019185851A1 (fr) 2018-03-28 2019-10-03 Croda International Plc Dispersants polymères agrochimiques
WO2022167655A1 (fr) * 2021-02-08 2022-08-11 Rhodia Operations Polymère de polyester biodégradable à libération de sol biodégradable et composition de nettoyage le comprenant

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4427557A (en) * 1981-05-14 1984-01-24 Ici Americas Inc. Anionic textile treating compositions
US5019389A (en) 1988-10-13 1991-05-28 University Of Arkansas Method of controlling crop and plant pests
EP0763068B1 (fr) * 1994-05-30 2001-09-05 Rhodia Chimie Compositions detergentes comprenant des polyesters sulfones
US6168947B1 (en) 1999-02-11 2001-01-02 Food Industry Research And Development Institute Nematophagous fungus Esteya vermicola
US9887664B2 (en) 2015-03-04 2018-02-06 David Lawrence Hammers Solar panel module with increased volume of solar production
WO2019185851A1 (fr) 2018-03-28 2019-10-03 Croda International Plc Dispersants polymères agrochimiques
US20210029989A1 (en) * 2018-03-28 2021-02-04 Croda International Plc Agrochemical polymer dispersants
WO2022167655A1 (fr) * 2021-02-08 2022-08-11 Rhodia Operations Polymère de polyester biodégradable à libération de sol biodégradable et composition de nettoyage le comprenant

Non-Patent Citations (3)

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Title
"Pesticide Manual", 2013, THE BRITISH CROP PROTECTION COUNCIL
NEMATOLOGY ADVANCES AND PERSPECTIVES, vol. 2, 2004
TODAR'S ONLINE TEXTBOOK OF BACTERIOLOGY, 2009

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