WO2019199752A1 - Functional fluoropolymers - Google Patents

Functional fluoropolymers Download PDF

Info

Publication number
WO2019199752A1
WO2019199752A1 PCT/US2019/026490 US2019026490W WO2019199752A1 WO 2019199752 A1 WO2019199752 A1 WO 2019199752A1 US 2019026490 W US2019026490 W US 2019026490W WO 2019199752 A1 WO2019199752 A1 WO 2019199752A1
Authority
WO
WIPO (PCT)
Prior art keywords
copolymer
monomer
fluorinated
lithium
formulation
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.)
Ceased
Application number
PCT/US2019/026490
Other languages
French (fr)
Inventor
James T. Goldbach
Wensheng He
Andrew P. Kahn
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.)
Arkema Inc
Original Assignee
Arkema Inc
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 Arkema Inc filed Critical Arkema Inc
Priority to EP19784265.1A priority Critical patent/EP3774714B1/en
Priority to CN201980024552.7A priority patent/CN111954657A/en
Priority to US17/045,263 priority patent/US12435174B2/en
Priority to KR1020207032363A priority patent/KR102836859B1/en
Priority to JP2020555440A priority patent/JP7535947B2/en
Publication of WO2019199752A1 publication Critical patent/WO2019199752A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/02—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polycarbonates or saturated polyesters
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C21/00—Acyclic unsaturated compounds containing halogen atoms
    • C07C21/02—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds
    • C07C21/18—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds containing fluorine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/52—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/52—Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
    • C07C69/533—Monocarboxylic acid esters having only one carbon-to-carbon double bond
    • C07C69/54—Acrylic acid esters; Methacrylic acid esters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
    • C08F214/18—Monomers containing fluorine
    • C08F214/22—Vinylidene fluoride
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10—Esters
    • C08F220/22—Esters containing halogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00—Polymerisation catalysts
    • C08F4/28—Oxygen or compounds releasing free oxygen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/02—Elements
    • C08K3/04—Carbon
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C08K3/22—Oxides; Hydroxides of metals
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/32—Phosphorus-containing compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C08L27/16—Homopolymers or copolymers or vinylidene fluoride
    • 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
    • C09D127/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
    • C09D127/02—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
    • C09D127/12—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C09D127/16—Homopolymers or copolymers of vinylidene fluoride
    • 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
    • C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04—Homopolymers or copolymers of esters
    • C09D133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
    • C09D133/16—Homopolymers or copolymers of esters containing halogen atoms
    • 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
    • C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
    • C09D151/08—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/04—Processes of manufacture in general
    • H01M4/0402—Methods of deposition of the material
    • H01M4/0404—Methods of deposition of the material by coating on electrode collectors
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/621—Binders
    • H01M4/622—Binders being polymers
    • H01M4/623—Binders being polymers fluorinated polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C08K3/22—Oxides; Hydroxides of metals
    • C08K2003/2203—Oxides; Hydroxides of metals of lithium
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C08K3/22—Oxides; Hydroxides of metals
    • C08K2003/2227—Oxides; Hydroxides of metals of aluminium
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C08K3/22—Oxides; Hydroxides of metals
    • C08K2003/2262—Oxides; Hydroxides of metals of manganese
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C08K3/22—Oxides; Hydroxides of metals
    • C08K2003/2289—Oxides; Hydroxides of metals of cobalt
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C08K3/22—Oxides; Hydroxides of metals
    • C08K2003/2293—Oxides; Hydroxides of metals of nickel
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/32—Phosphorus-containing compounds
    • C08K2003/321—Phosphates
    • C08K2003/324—Alkali metal phosphate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/32—Phosphorus-containing compounds
    • C08K2003/321—Phosphates
    • C08K2003/328—Phosphates of heavy metals
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00—Specific properties of additives
    • C08K2201/001—Conductive additives
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00—Specific properties of additives
    • C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M2004/026—Electrodes composed of, or comprising, active material characterised by the polarity
    • H01M2004/028—Positive electrodes
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries

Definitions

  • the invention relates to novel linear, semi-crystalline, functional fluoropolymers that have been obtained by copolymerizing a fluorinated vinylic monomer and a hydrophilic (meth)acrylic comonomer bearing a halogen functionality. At most 10.0 weight percent of the (meth)acrylic comonomer units are present in the copolymer as single monomer units between two fluoromonomer units.
  • the invention also relates to a process for forming the fluoromonomers/(meth) acrylic copolymer.
  • Fluoropolymers are traditionally used for applications requiring special properties, such as low surface energy, high resistance to chemical attack, aging resistance, and electrochemical stability.
  • these advantageous properties also make fluoropolymers difficult to work with and limits their applications.
  • the lack of functional groups on the fluoropolymers makes them difficult: to adhere to substrates, to facilitate cross-linking, to provide sites for subsequent chemical modification, to be wetted by water, and to add hydrophilic characteristics.
  • fluorinated polymers having modified properties, such as functional groups which can augment their properties.
  • US 5,415,958 discloses copolymerization of vinylidene fluoride with an unsaturated dibasic acid monoester polar monomer, to introduce carbonyl groups to the backbone of PVDF in order to improve its adhesion to different substrates.
  • US 8,337,725 discloses copolymerization of vinylidene fluoride with at least one hydrophilic (meth)acrylic monomer of formula:
  • each of R 1 , R2, R3 is independently a hydrogen atom or a C1-C3 hydrocarbon group
  • R OH is a hydrogen or a C1-C5 hydrocarbon moiety comprising at least one hydroxyl group.
  • the invention relates to a fluorinated copolymer comprising a fluorinated vinylic monomer and a halogenated monomer (1):
  • Ri, R 2 , and R 3 is a hydrogen or a halogen (F, Cl, Br, I), and at least one is a halogen;
  • R 4 is hydrogen, a C i to C 10 linear, branched, aryl, or cycloalkyl group, a Ci to C1 ⁇ 2 fluorinated linear, branched, aryl or cycloalkyl group, a fluorinated oligomer of hexfluoropropylene oxide, an alkali metal (lithium, sodium, potassium, rubidium, cesium), ammonium, alkylammonium, or alkylarylammonium ion.
  • the invention further relates to a formulation comprising the fluorinated copolymer in a solvent, and may further comprise conductive carbon additives and active material particles.
  • Active materials for lithium ion battery cathode formulation include, but are not limited to: lithium iron phosphate (LFP), lithium nickel manganese cobalt oxide (NMC), lithium-manganese-cobalt- oxide (LCO), lithium-nickel-cobalt-aluminum oxide (NCA), lithium-manganese oxide (LMO), lithium-nickel-manganese-oxide (LNMO), and lithium manganese iron phosphate (LMFP).
  • Active materials for anode formulation include, but are not limited to graphite, hard carbon, soft carbon, graphene, silicon, silicon monoxide (SiO), tin, or lithium titanate (LTO).
  • the invention further contemplates a process for preparing the fluorinated copolymer in an aqueous reaction medium, comprising: a) forming an aqueous emulsion comprising at least one initiator, a stabilizer, at least one fluoromonomer, and a halogenated monomer (1) as defined above, b) initiating copolymerization of said at least one fluoromonomer with said halogenated monomer (1) with stirring, under heat and super- atmospheric pressure.
  • the invention further relates to articles formed from the fluorinated copolymer, which benefit from the special properties of the functional copolymer.
  • These articles find uses in applications such as for: an electrode or separator for a battery or capacitor; a hydrophilic porous membrane or hollow fiber membrane; an article coated on at least one surface with said functional fluoropolymer, impregnation of woven and unwoven fibers, and a multi-layer construction wherein said functional fluoropolymer forms a tie layer between a fluoropolymer layer and a polymer layer that is incompatible with said fluoropolymer layer.
  • “Copolymer” is used to mean a polymer having two or more different monomer units. “Polymer” is used to mean both homopolymer and copolymers. Polymers may be straight chain, branched, star comb, block, or any other structure. The polymers may be homogeneous, heterogeneous, and may have a gradient distribution of co-monomer units. All references cited are incorporated herein by reference. As used herein, unless otherwise described, percent shall mean weight percent. Unless otherwise stated, molecular weight is a weight average molecular weight as measured by GPC, using a polymethyl methacrylate standard.
  • soluble fraction/ gel fraction or soluble faction molecular weight after extraction from gel is used.
  • Crystallinity and melting temperature are measure by DSC as described in ASTM D3418 at heating rate of 10 C/min. Melt viscosity is measured in accordance with ASTM D3835 at 230°C expressed in k Poise @ 100 Sec A (-l)
  • Fluoropolymers particularly poly(vinylidene fluoride) (PVDF) and its copolymers, find application as the binder in electrode articles used in lithium ion batteries.
  • PVDF poly(vinylidene fluoride)
  • One key binder performance matrix is determined by an adhesion test whereby a formulated electrode is subjected to a peel test. Improved binding performance increases the potential to reduce the overall binder loading, increasing active material loading and improving battery capacity and energy density.
  • the functional fluoropolymers provide enhanced properties compared to the fluoropolymer, such as increased adhesion and hydrophilic characteristics.
  • the fluoropolymer of the invention may be used in applications benefiting from a functional fluoropolymer including as binders in electrode-forming compositions and separator compositions, or in forming hydrophilic membranes and hollow fibers.
  • the invention solves the above-cited problems by providing a fluorinated copolymer comprising a fluorinated vinylic monomer and a monomer (1):
  • Ri, R 2 , and R 3 is a hydrogen or a halogen (F, Cl, Br, I), and at least one is a halogen;
  • R 4 is hydrogen, a Ci to C 1 ⁇ 2 linear, branched, aryl, or cycloalkyl group, a Ci to C1 ⁇ 2 fluorinated linear, branched, aryl or cycloalkyl group, a fluorinated oligomer of hexfluoropropylene oxide, an alkali metal (lithium, sodium, potassium, rubidium, cesium), ammonium, alkylammonium, or alkylarylammonium ion.
  • an alkali metal lithium, sodium, potassium, rubidium, cesium
  • the fluorinated vinylic monomer is selected from the group comprising: vinylidene fluoride (VDF), tetrafluoroethylene (TFE), trifluoroethylene (TrFE), chlorotrifluoroethylene (CTFE), hexafluoropropene (HFP), vinyl fluoride (VF), hexafluoroisobutylene (HFIB), perfluorobutylethylene (PFBE), pentafluoropropene, 3,3,3-trifluoro-l-propene, 2-trifluoromethyl- 3,3,3-trifluoropropene, 2,3,3,3-tetrafluoropropene, fluorinated vinyl ethers including perfluoromethyl ether (PMVE), perfluoroethylvinyl ether (PEVE), perfluoropropylvinyl ether (PPVE), perfluorobutylvinyl ether (PBVE), longer alkyl chain perfluorinated vinyl ether
  • the functional copolymer according to the invention is further characterized by the following embodiments.
  • the fluorinated copolymer comprises up to 10 wt % of Monomer (1), preferably 0.001 to 10.0 wt%, preferably from 0.01 to l0.0wt% of Monomer (1) and 90.0 to 99.99wt% of fluorinated vinylic monomer.
  • the fluorinated copolymer comprises vinylidene fluoride and Monomer (1).
  • the fluorinated copolymer comprises vinylidene fluoride and Monomer (1), wherein Ri is fluorine.
  • the fluorinated copolymer comprises vinylidene fluoride and Monomer (1), wherein Ri is fluorine and R 4 is Ci to C1 ⁇ 2 linear, branched or cycloalkyl group.
  • the fluorinated copolymer comprises vinylidene fluoride and Monomer (1), wherein Ri and R 2 are fluorine and R 4 is Ci to Ci 6 linear, branched or cycloalkyl group.
  • the fluorinated copolymer comprises vinylidene fluoride and Monomer (1), wherein Ri, R 2 and R 3 are fluorine and R 4 is Ci to C1 ⁇ 2 linear, branched or cycloalkyl group.
  • the fluorinated copolymer comprises vinylidene fluoride and Monomer (1), wherein Ri is fluorine and R 4 is hydrogen or an alkali metal, ammonium, or alkylammonium.
  • the fluorinated copolymer comprises vinylidene fluoride and Monomer (1), wherein Ri and R 2 are fluorine and R 4 is hydrogen or an alkali metal, ammonium, or alkylammonium.
  • the fluorinated copolymer comprises vinylidene fluoride and Monomer (1), wherein Ri, R 2 and R 3 are fluorine and R 4 is hydrogen or an alkali metal, ammonium, or alkylammonium.
  • Monomer (1) is randomly copolymerized as determined by nuclear magnetic resonance ( 19 F NMR and 'H NMR) of Monomer (1).
  • the invention further relates to a formulation comprising the fluorinated copolymer in a solvent.
  • the solvent is preferably chosen from: n-methylpyrrolidone (NMP), dimethylsulfoxide (DMSO), N,N-dimethylformamide (DMF), triethylphosphite (TEP), acetone, tetrahydrofuran, methyl ethylketone (MEK), methyl isobutyl ketone (MiBK), ethyl acetate (EA), butyl acetate (BA), ethylene carbonate (EC), propylene carbonate (PC), dimethyl carbonate (DMC), diethyl carbonate (DEC) or ethyl methyl carbonate (EMC).
  • NMP n-methylpyrrolidone
  • DMSO dimethylsulfoxide
  • DMF N,N-dimethylformamide
  • TEP triethylphosphite
  • MEK methyl e
  • the formulation further comprises conductive carbon additives and active material particles in suspension in said solvent.
  • Such formulation is particularly suitable for forming battery electrode films, notably positive (cathode) electrode or negative (anode) electrod for a lithium ion battery.
  • Active material for lithium ion battery cathode formulation can be selected from the group, not limiting to, lithium iron phosphate (LFP), lithium nickel manganese cobalt oxide (NMC), lithium-manganese-cobalt-oxide (LCO), lithium-nickel- cobalt-aluminum oxide (NCA), lithium-manganese oxide (LMO), lithium-nickel-manganese- oxide (LNMO) , and lithium manganese iron phosphate (LMFP).
  • Active material for anode formulation can be from graphite, hard carbon, soft carbon, graphene, silicon, silicon monoxide (SiO), tin, or lithium titanate (LTO).
  • the invention encompasses a battery comprising the fluorinated copolymer described herein. [0031]
  • the invention further contemplates a process for preparing the fluorinated copolymer in an aqueous reaction medium, comprising:
  • a) forming an aqueous emulsion comprising at least one initiator, a stabilizer, at least one fluorinated vinylic monomer, and a halogenated monomer (1) as defined above, b) initiating copolymerization of said at least one fluorinated vinylic monomer with said halogenated monomer (1) with stirring, under heat and super- atmospheric pressure.
  • a polymerization reaction in accordance with the present invention may be carried out by charging a reactor with water (preferably deionized water), at least one fluorinated vinylic monomer, at least one halogenated Monomer (1) as defined above and optionally, one or more of a surfactant, a chain-transfer agent and/or an antifoulant. Air may be purged from the reactor prior to the introduction of the fluoromonomer. Water is added to the reactor before bringing the reactor to the desired starting temperature, but the other materials may be added before or after bringing the reactor to temperature. At least one radical initiator is added to start and maintain the polymerization reaction.
  • Additional vinylic fluoromonomer(s) and/or additional functional monomer may be optionally added to replenish monomer that is consumed, and the other materials may be optionally added during the course of the polymerization to maintain the reaction and control the final product properties.
  • all monomer components will be fed at a controlled ratio (to each other) to maintain reaction pressure
  • the Monomers (1) comonomers may be used in the reactor in an amount, for example, of from about 0.001 to about 15 weight percent, preferably from about 0.01 to about 15 weight percent based on total monomer. Preferably they are used in an amount from about 0.001 to about 10 weight percent, preferably 0.01 to about 10 weight percent based on total monomer. In various embodiments, the total amount of hydrophilic monomer(s) is at least 0.001, at least 0.01, at least 0.05, at least 0.1, at least 1.0 or at least 2.0 weight percent based on total monomer. In other embodiments, the total amount of hydrophilic monomer does not exceed 13.0, 10.0, 9.0, 7.0, 6.0, 5.0 weight percent based on total monomer.
  • the hydrophilic (meth)acrylic comonomer may be used in solution such as in aqueous solution for convenient handling.
  • two or more different functional acrylates was found to provide increased adhesion. While not being bound by any particular theory, it is believed that different functionalities, for example an alcohol and acid functionality, could react or crosslink to form ester groups.
  • the two or more different functionalities preferably are present in the same terpolymer, but could also be a blend of two or more different copolymers.
  • the surfactant used in the polymerization can be any surfactant known in the art to be useful in PVDF emulsion polymerization, including perfluorinated, partially fluorinated, and non- fluorinated surfactants.
  • the PVDF emulsion of the present disclosure can be fluorosurfactant free, with no fluoro surfactants being used in any part of the polymerization.
  • Non-fluorinated surfactants useful in the PVDF polymerization could be both ionic and non-ionic in nature including, but are not limited to, 3-allyloxy-2-hydroxy-l-propane sulfonic acid salt, polyvinylphosphonic acid, polyacrylic acids, polyvinyl sulfonic acid, and salts thereof, polyethylene glycol and/or polypropylene glycol and the block copolymers thereof, alkyl phosphonates and siloxane-based surfactants.
  • Surfactants can also be used in combination with hydrophilic (meth)acrylic comonomer to provide further stability to the polymer emulsion.
  • Preferred surfactants are non-fluorinated hydrocarbon surfactants, siloxane surfactants or a combination thereof.
  • a hydrophilic (meth)acrylic comonomer can be used in combination with sodium dodecyl benzene sulfonate (SDDBS), sodium octyl sulfonate, sodium lauryl sulfate, ammonium lauryl sulfate, or sodium laureth sulfate, among others.
  • no fluorosurfactant is present in the aqueous emulsion and/or no fluorosurfactant is introduced during copolymerization of the fluorinated vinylic monomer with the hydrophilic (meth)acrylic comonomer.
  • the stabilizer is a poly electrolyte.
  • the stabilizer of the polymer emulsion is a functionalized cellulose.
  • initiator and the expressions "radical initiator” and “free radical initiator” refer to a chemical that is capable of providing a source of free radicals, either induced spontaneously, or by exposure to heat or light. Examples of suitable initiators include peroxides, peroxydicarbonates and azo compounds. “Initiators” also includes redox systems useful in providing a source of free radicals.
  • radical and the expression “free radical” refer to a chemical species that contains at least one unpaired electron.
  • the radical initiator is added to the reaction mixture in an amount sufficient to initiate and maintain the polymerization reaction at a desired reaction rate.
  • the order of addition may vary according to the desired process and latex emulsion characteristics.
  • the radical initiator may comprise a persulfate salt, such as sodium persulfate, potassium persulfate, or ammonium persulfate.
  • the amount of persulfate salt added to the reaction mixture may, for example, be from about 0.002 to about 1.0 weight percent.
  • the radical initiator may comprise an organic peroxide such as an alkyl, dialkyl, or diacyl peroxide, peroxydicarbonates, and peroxy esters or mixtures thereof.
  • a preferred dialkyl peroxide is di-tert-butylperoxide (DTBP), which may be added to the reaction mixture in an amount from about 0.01 to about 5 weight percent on total monomer, and is preferably added in an amount from about 0.05 to about 2.5 weight percent on total monomer.
  • Preferred peroxydicarbonate initiators are di-n-propyl peroxydicarbonate and diisopropyl peroxydicarbonate, which may be added to the reaction mixture in an amount from about 0.5 to about 2.5 weight percent on total monomer.
  • Peroxy ester initiators include tert-amyl peroxypivalate, tertbutyl peroxypivalate, and succinic acid peroxide.
  • the radical initiator may comprise an azo initiator, such as 2,2'- azobis(2 methyl- propionamidine)dihydrochloride.
  • the radical initiator may comprise a redox system.
  • redox system is meant a system comprising an oxidizing agent, a reducing agent and optionally, a promoter as an electron transfer medium.
  • Oxidizing agents include, for example, persulfate salts; peroxides, such as hydrogen peroxide; hydroperoxides such as tert-butyl hydroperoxide and cumene hydroperoxide; and oxidizing metal salts such as, for example, ferric sulfate.
  • Reducing agents include, for example, sodium formaldehyde sulfoxylate, sodium and potassium sulfite, ascorbic acid, bisulfite, metabisulfite, and reduced metal salts.
  • the promoter is a component of the redox system which, in different oxidation states, is capable of reacting with both the oxidant and the reducing agent, thereby accelerating the overall reaction. Promoters include, for example, transition metal salts such as ferrous sulfate.
  • the oxidizing agent and the reducing agent may be utilized in an amount from about 0.01 to about 0.5 weight percent on total monomer.
  • the optional promoter may be utilized in an amount from about 0.005 to about 0.025 weight percent on total monomer. Redox systems are described in G.S. Misra and U.D.N. Bajpai, Prog. Polym. Sci., 1982, 8(1-2), pp. 61-131.
  • Chain-transfer agents are added to the polymerization to regulate the molecular weight of the product. They may be added to a polymerization in a single portion at the beginning of the reaction, or incrementally or continuously throughout the reaction. The amount and mode of addition of chain-transfer agent depend on the activity of the particular chain transfer agent employed, and on the desired molecular weight of the polymer product. The amount of chain- transfer agent added to the polymerization reaction is preferably from about 0.05 to about 5 weight percent, more preferably from about 0.1 to about 2 weight percent based on the total weight of monomer added to the reaction mixture.
  • Oxygenated compounds such as alcohols, carbonates, ketones, esters, and ethers may serve as chain-transfer agents.
  • oxygenated compounds useful as chain-transfer agents include isopropyl alcohol, as described in U.S. Patent 4,360,652.
  • Other classes of compounds which may serve as chain-transfer agents in the polymerization of halogen-containing monomers include, for example, halocarbons and hydrohalocarbons, such as chlorocarbons.
  • Alkanes such as ethane and propane may also function as chain-transfer agents.
  • the polymerization reaction mixture may optionally contain a buffering agent to maintain a controlled pH throughout the polymerization reaction.
  • the pH is preferably controlled within the range of from about 4 to about 8, to minimize undesirable color development in the product.
  • Buffering agents may comprise an organic or inorganic acid or alkali metal salt thereof, or base or salt of such organic or inorganic acid, that has at least one pK a value and/or pK b value in the range of from about 4 to about 10, preferably from about 4.5 to about 9.5.
  • Preferred buffering agents in the practice of the invention include, for example, phosphate buffers and acetate buffers.
  • a "phosphate buffer” is a salt or a mixture of salts of phosphoric acid.
  • An “acetate buffer” is a salt of acetic acid.
  • Buffering agents are preferably employed where potassium persulfate is employed as the radical initiator.
  • a preferred buffering agent for use with persulfate radical initiators is sodium acetate.
  • a preferred amount of sodium acetate buffer is from about 50 wt.% to about 150 wt.%, based on the weight of persulfate initiator added to the reaction.
  • the initiator feed comprises approximately equal weights of potassium persulfate and sodium acetate in aqueous solution.
  • the addition of a paraffin wax or hydrocarbon oil to the reaction serves as an antifoulant to minimize or prevent polymer adhesions to the reactor components. Any long chain saturated hydrocarbon wax or oil can perform this function.
  • the amount of oil or wax added to the reactor is an amount which serves to minimize the formation of polymer adhesions on the reactor components. The amount is generally proportional to the interior surface area of the reactor and may vary from about 1 to about 40 mg per square centimeter of reactor interior surface area.
  • the amount of paraffin wax or hydrocarbon oil is preferably about 5 mg/cm 2 of the reactor interior surface area.
  • the temperature used for polymerization may vary, for example, from 20-130 degrees Celsius, depending on the initiator system chosen.
  • the polymerization temperature is preferably from 35-130 degrees Celsius, and most preferably from 70-125 degrees Celsius.
  • the pressure used for polymerization may vary from 280-20,000 kPa, depending on the capabilities of the reaction equipment, the initiator system chosen, and the monomer selection.
  • the polymerization pressure is preferably from 2,000-11,000 kPa, and most preferably from 2,750-6,900 kPa.
  • the polymerization occurs under stirring or other agitation.
  • the stirring/agitation may be constant, or may be varied to optimize process conditions during the course of the polymerization. In one embodiment, both multiple stirring speeds and multiple temperatures are used for controlling the reaction.
  • a pressurized polymerization reactor equipped with a stirrer and heat control means is charged with water, preferably deionized water, one or more halogenated monomers (1) and at least one fluorinated vinylic monomer.
  • the mixture may optionally contain one or more of a surfactant, a buffering agent, an antifoulant or a chain-transfer agent for molecular weight regulation of the polymer product.
  • air Prior to introduction of the monomer or monomers, air is preferably removed from the reactor in order to obtain an oxygen-free environment for the polymerization reaction.
  • the order in which the polymerization components are assembled may be varied, although it is generally preferred that at least a portion of the Monomer (1) is present in the aqueous reaction medium prior to the initiation of the polymerization of the fluorinated vinylic monomer. An additional amount of Monomer (1) may be fed to the reactor during the reaction.
  • water, initiator, Monomer (1) and optionally surfactant, antifoulant, chain transfer agent and/or buffer are charged to the reactor, and the reactor heated to the desired reaction temperature.
  • the fluorinated vinylic monomer(s) is(are) then fed into the reactor, preferably at a rate which provides an essentially constant pressure.
  • the fluorinated vinylic monomer, Monomer (1) and initiator can be fed to the reactor, along with one or more of the optional ingredients.
  • Other variations for fluoropolymer copolymerization processes are contemplated, as known in the art.
  • the monomer feed is terminated when the desired weight of monomer has been fed to the reactor. Additional radical initiator is optionally added, and the reaction is allowed to react out for a suitable amount of time. The reactor pressure drops as the monomer within the reactor is consumed.
  • the reactor Upon completion of the copolymerization reaction, the reactor is brought to ambient temperature and the residual unreacted monomer is vented to atmospheric pressure.
  • the aqueous reaction medium containing the copolymer is then recovered from the reactor as a latex.
  • the latex consists of a stable mixture of the reaction components, i.e., water, Monomer (1), initiator (and/or decomposition products of the initiator) and copolymer solids.
  • the latex contains from about 10 to about 50 weight percent copolymer solids.
  • the polymer in the latex may be in the form of small particles having a size range of from about 30 nm to about 800 nm.
  • the product of the copolymerization is a latex which can be used in that form, usually after filtration of solid byproducts from the polymerization process, or which can be coagulated to isolate the solids, which may then be washed and dried.
  • the latex can be stabilized by the addition of a surfactant, which may be the same as or different from the surfactant present during polymerization (if any).
  • This later added surfactant may, for example, be an ionic or non-ionic surfactant.
  • no fluorosurfactant is added to the latex.
  • the latex may be coagulated mechanically or by the addition of salts or acids, and then isolated by well-known means such as by filtration. Once isolated, solid product can be purified by washing or other techniques, and it may be dried for use as a powder, which can be further processed into granules, pellets or the like.
  • the functional copolymer according to the invention is applied to a substrate, as a latex in water or as a solvent solution, the solvent being chosen among those listed above.
  • a primer layer can be applied to the substrate, before the layer of functional copolymer.
  • said substrate is porous, for example a porous membrane.
  • PVDF copolymer of the invention is first dissolved in N-methylpyrrolidone (NMP) solvent, typically in 5-l0wt% concentration.
  • NMP N-methylpyrrolidone
  • Conductive carbon additive such as SuperP-Li from Timcal
  • active material such as Celcore® NMC622 (Umicore), and small amount of NMP are added to the mixture, and mixed to form a thick and uniform paste, typically 60s at 2000rpm.
  • the cathode slurry is then cast onto aluminum foil (15mhi thickness) using adjustable doctor blade on an automatic film applicator (Elcometer 4340).
  • the wet casting is then transferred to a convection oven, and dried at 120C for 30min.
  • the electrode is calendered using a roll mill (IRM, international roll mill), to a final density of 3.2-3.6 g/cm3, with a typical value of 3.4g/cm3.
  • the typical areal mass loading of the dry cathode is 180-220 g/m2.
  • Peel strengths for cathodes were obtained via a 180° peel test using ASTM D903 with three modifications. The first modification was that the extension rate used was 50 mm/minute (peel rate of 25 mm/minute), electrodes were tested one day after fabrication, and the electrode was bonded to the alignment plate using double sided paper tape (3M Company, type 401M) with the flexible aluminum foil current collector peeled affixed in the testing grips.
  • the first modification was that the extension rate used was 50 mm/minute (peel rate of 25 mm/minute), electrodes were tested one day after fabrication, and the electrode was bonded to the alignment plate using double sided paper tape (3M Company, type 401M) with the flexible aluminum foil current collector peeled affixed in the testing grips.
  • Example 1 To a 2 gallon autoclave were added 3500g of deionized water, 9.2g of low molecular weight poly(acrylic acid) (BASF CP-10S), and 0.5g of methyl 2-fluoroacrylate (MFA). The autoclave was agitated, heated to 100C and pressurized to 650psi with vinylidene fluoride. A 2.0wt% feed of potassium persulfate was started at 2.0mL/min. Upon start of pressure drop, an additional feed of MFA was started at 0.25mL/min. and pressure was maintained by additional VDF feed. Feeds were continued in this fashion, increasing MFA feed rate to moderate instantaneous VDF feed demand to maintain a range of 500-1500g/hr.
  • BASF CP-10S low molecular weight poly(acrylic acid)
  • MFA methyl 2-fluoroacrylate
  • MFA feed was increased in this fashion up to l.OmL/min. All feeds were continued until a total of 1650g of VDF had been fed to the reactor, corresponding to 69.6g of MFA. Monomer feeds were stopped and the pressure was allowed to autogenously decrease for 10 minutes at which point the reactor was vented to atmospheric pressure and cooled to room temperature. Latex was discharged from the reactor and dried in a convection oven overnight. 4993g of latex was recovered with solids of 31 wt%.
  • Example 2 To a 2 gallon autoclave were added 3500g of deionized water, 9.2g of low molecular weight poly(acrylic acid) solution (BASF CP-10S), and 25mL of sodium 2-fluoroacrylate (SFA) as 5.25wt% solution in deionized water. The autoclave was agitated, heated to 100C and pressurized to 650psi with vinylidene fluoride. A 2.0wt% feed of potassium persulfate was started at 2.0mF/min. Upon start of pressure drop, an additional feed of SFA solution was started at 2.0mF/min. and pressure was maintained by additional VDF feed.
  • BASF CP-10S low molecular weight poly(acrylic acid) solution
  • SFA sodium 2-fluoroacrylate
  • Example 3 An identical procedure as outlined in Example 1 was used except a reaction temperature of 83C was used and total of 1.15% MFA was fed vs. total VDF. Fluid latex was recovered with solids of 33.5 wt%.
  • Example 4 An identical procedure as outlined in Example 1 was used except a reaction temperature of 83C was used and total of 2.30% MFA was fed vs. total VDF. Fluid latex was recovered with solids of 30.5 wt%.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Electric Double-Layer Capacitors Or The Like (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

The invention relates to novel linear, semi-crystalline, functional fluoropolymers that have been obtained by copolymerizing a fluorinated vinylic monomer and a hydrophilic (meth)acrylic comonomer bearing a halogen functionality.

Description

FUNCTIONAL FLUOROPOLYMERS
FIELD OF THE INVENTION
[0001] The invention relates to novel linear, semi-crystalline, functional fluoropolymers that have been obtained by copolymerizing a fluorinated vinylic monomer and a hydrophilic (meth)acrylic comonomer bearing a halogen functionality. At most 10.0 weight percent of the (meth)acrylic comonomer units are present in the copolymer as single monomer units between two fluoromonomer units. The invention also relates to a process for forming the fluoromonomers/(meth) acrylic copolymer.
BACKGROUND OF THE RELATED ART
[0002] Fluoropolymers are traditionally used for applications requiring special properties, such as low surface energy, high resistance to chemical attack, aging resistance, and electrochemical stability. However, these advantageous properties also make fluoropolymers difficult to work with and limits their applications. For example, the lack of functional groups on the fluoropolymers makes them difficult: to adhere to substrates, to facilitate cross-linking, to provide sites for subsequent chemical modification, to be wetted by water, and to add hydrophilic characteristics. There is a need for fluorinated polymers having modified properties, such as functional groups, which can augment their properties.
[0003] However it is difficult to add functional monomer units directly into the polymerizing polymer backbone, especially in a random manner, due to the aggressive nature of the fluorine- containing free radicals. Functionality has been added by several means, such as, by direct copolymerization of a functional monomer with the fluoromonomers, and by a post polymerization grafting mechanism, such as the grafting of maleic anhydride onto a polyvinylidene fluoride homopolymer or copolymer, as described in US 7,241,817, to form KYNAR® ADX resins available from Arkema Inc. (Pennsylvania, USA). WO 2013/110740 and US 7,351,498 further describe functionalization of a fluoropolymer by monomer grafting or by copolymerization.
[0004] US 5,415,958 discloses copolymerization of vinylidene fluoride with an unsaturated dibasic acid monoester polar monomer, to introduce carbonyl groups to the backbone of PVDF in order to improve its adhesion to different substrates. [0005] US 8,337,725 discloses copolymerization of vinylidene fluoride with at least one hydrophilic (meth)acrylic monomer of formula:
Figure imgf000003_0001
[0006] wherein each of R 1 , R2, R3 , equal or different from each other, is independently a hydrogen atom or a C1-C3 hydrocarbon group, and ROH is a hydrogen or a C1-C5 hydrocarbon moiety comprising at least one hydroxyl group.
[0007] There is a need to further improve the adhesion performance of fluorinated polymers.
[0008] The art is silent as to functional fluoropolymers obtained by copolymerizing a fluorinated vinylic monomer and a hydrophilic (meth)acrylic comonomer bearing a halogen functionality, that allow for improved adhesion to a substrate, when compared to the non-functional fluoropolymer, while maintaining good mechanical and thermal properties.
BRIEF SUMMARY OF THE INVENTION
[0009] The invention relates to a fluorinated copolymer comprising a fluorinated vinylic monomer and a halogenated monomer (1):
Figure imgf000003_0002
Monomer (1) wherein:
Ri, R2, and R3 is a hydrogen or a halogen (F, Cl, Br, I), and at least one is a halogen;
R4 is hydrogen, a C i to C 10 linear, branched, aryl, or cycloalkyl group, a Ci to C½ fluorinated linear, branched, aryl or cycloalkyl group, a fluorinated oligomer of hexfluoropropylene oxide, an alkali metal (lithium, sodium, potassium, rubidium, cesium), ammonium, alkylammonium, or alkylarylammonium ion. [0010] The invention further relates to a formulation comprising the fluorinated copolymer in a solvent, and may further comprise conductive carbon additives and active material particles. Active materials for lithium ion battery cathode formulation include, but are not limited to: lithium iron phosphate (LFP), lithium nickel manganese cobalt oxide (NMC), lithium-manganese-cobalt- oxide (LCO), lithium-nickel-cobalt-aluminum oxide (NCA), lithium-manganese oxide (LMO), lithium-nickel-manganese-oxide (LNMO), and lithium manganese iron phosphate (LMFP). Active materials for anode formulation include, but are not limited to graphite, hard carbon, soft carbon, graphene, silicon, silicon monoxide (SiO), tin, or lithium titanate (LTO).
[0011] The invention further contemplates a process for preparing the fluorinated copolymer in an aqueous reaction medium, comprising: a) forming an aqueous emulsion comprising at least one initiator, a stabilizer, at least one fluoromonomer, and a halogenated monomer (1) as defined above, b) initiating copolymerization of said at least one fluoromonomer with said halogenated monomer (1) with stirring, under heat and super- atmospheric pressure.
[0012] The invention further relates to articles formed from the fluorinated copolymer, which benefit from the special properties of the functional copolymer. These articles find uses in applications such as for: an electrode or separator for a battery or capacitor; a hydrophilic porous membrane or hollow fiber membrane; an article coated on at least one surface with said functional fluoropolymer, impregnation of woven and unwoven fibers, and a multi-layer construction wherein said functional fluoropolymer forms a tie layer between a fluoropolymer layer and a polymer layer that is incompatible with said fluoropolymer layer.
[0013]“Copolymer” is used to mean a polymer having two or more different monomer units. “Polymer” is used to mean both homopolymer and copolymers. Polymers may be straight chain, branched, star comb, block, or any other structure. The polymers may be homogeneous, heterogeneous, and may have a gradient distribution of co-monomer units. All references cited are incorporated herein by reference. As used herein, unless otherwise described, percent shall mean weight percent. Unless otherwise stated, molecular weight is a weight average molecular weight as measured by GPC, using a polymethyl methacrylate standard. In cases where the polymer contains some cross-linking, and GPC cannot be applied due to an insoluble polymer fraction, soluble fraction/ gel fraction or soluble faction molecular weight after extraction from gel is used. Crystallinity and melting temperature are measure by DSC as described in ASTM D3418 at heating rate of 10 C/min. Melt viscosity is measured in accordance with ASTM D3835 at 230°C expressed in k Poise @ 100 SecA(-l)
DETAILED DESCRIPTION OF THE INVENTION
[0014] Fluoropolymers, particularly poly(vinylidene fluoride) (PVDF) and its copolymers, find application as the binder in electrode articles used in lithium ion batteries. As the demand for greater energy density and battery performance intensifies, the need for reduction of the binder content in the electrodes has increased. To reduce the binder content, it is paramount to increase the performance of the binder material. One key binder performance matrix is determined by an adhesion test whereby a formulated electrode is subjected to a peel test. Improved binding performance increases the potential to reduce the overall binder loading, increasing active material loading and improving battery capacity and energy density. It has been shown that copolymers of fluorinated vinylic monomers with acid-functional comonomers lead to adhesion performance improvement. These approaches have also suffered from low reaction productivity, and difficulty to supply sufficient quantities of material to a rapidly-growing market. Here, we present a new copolymer and process with vastly improved productivity.
[0015] The functional fluoropolymers provide enhanced properties compared to the fluoropolymer, such as increased adhesion and hydrophilic characteristics. The fluoropolymer of the invention may be used in applications benefiting from a functional fluoropolymer including as binders in electrode-forming compositions and separator compositions, or in forming hydrophilic membranes and hollow fibers.
[0016] The invention solves the above-cited problems by providing a fluorinated copolymer comprising a fluorinated vinylic monomer and a monomer (1):
Figure imgf000005_0001
Monomer (1) wherein:
Ri, R2, and R3 is a hydrogen or a halogen (F, Cl, Br, I), and at least one is a halogen;
R4 is hydrogen, a Ci to C½ linear, branched, aryl, or cycloalkyl group, a Ci to C½ fluorinated linear, branched, aryl or cycloalkyl group, a fluorinated oligomer of hexfluoropropylene oxide, an alkali metal (lithium, sodium, potassium, rubidium, cesium), ammonium, alkylammonium, or alkylarylammonium ion.
[0017] The fluorinated vinylic monomer is selected from the group comprising: vinylidene fluoride (VDF), tetrafluoroethylene (TFE), trifluoroethylene (TrFE), chlorotrifluoroethylene (CTFE), hexafluoropropene (HFP), vinyl fluoride (VF), hexafluoroisobutylene (HFIB), perfluorobutylethylene (PFBE), pentafluoropropene, 3,3,3-trifluoro-l-propene, 2-trifluoromethyl- 3,3,3-trifluoropropene, 2,3,3,3-tetrafluoropropene, fluorinated vinyl ethers including perfluoromethyl ether (PMVE), perfluoroethylvinyl ether (PEVE), perfluoropropylvinyl ether (PPVE), perfluorobutylvinyl ether (PBVE), longer alkyl chain perfluorinated vinyl ethers, fluorinated dioxoles, partially- or per-fluorinated alpha olefins of C4 and higher, partially- or per fluorinated cyclic alkenes of C3 and higher, and combinations thereof.
[0018] The functional copolymer according to the invention is further characterized by the following embodiments.
[0019] According to one embodiment, the fluorinated copolymer comprises up to 10 wt % of Monomer (1), preferably 0.001 to 10.0 wt%, preferably from 0.01 to l0.0wt% of Monomer (1) and 90.0 to 99.99wt% of fluorinated vinylic monomer.
[0020] According to one embodiment, the fluorinated copolymer comprises vinylidene fluoride and Monomer (1).
[0021] According to one embodiment, the fluorinated copolymer comprises vinylidene fluoride and Monomer (1), wherein Ri is fluorine.
[0022] According to one embodiment, the fluorinated copolymer comprises vinylidene fluoride and Monomer (1), wherein Ri is fluorine and R4 is Ci to C½ linear, branched or cycloalkyl group.
[0023] According to one embodiment, the fluorinated copolymer comprises vinylidene fluoride and Monomer (1), wherein Ri and R2 are fluorine and R4 is Ci to Ci6 linear, branched or cycloalkyl group. [0024] According to one embodiment, the fluorinated copolymer comprises vinylidene fluoride and Monomer (1), wherein Ri, R2 and R3 are fluorine and R4 is Ci to C½ linear, branched or cycloalkyl group.
[0025] According to one embodiment, the fluorinated copolymer comprises vinylidene fluoride and Monomer (1), wherein Ri is fluorine and R4 is hydrogen or an alkali metal, ammonium, or alkylammonium.
[0026] According to one embodiment, the fluorinated copolymer comprises vinylidene fluoride and Monomer (1), wherein Ri and R2 are fluorine and R4 is hydrogen or an alkali metal, ammonium, or alkylammonium.
[0027] According to one embodiment, the fluorinated copolymer comprises vinylidene fluoride and Monomer (1), wherein Ri, R2 and R3 are fluorine and R4 is hydrogen or an alkali metal, ammonium, or alkylammonium.
[0028] According to one embodiment, Monomer (1) is randomly copolymerized as determined by nuclear magnetic resonance (19F NMR and 'H NMR) of Monomer (1).
[0029] The invention further relates to a formulation comprising the fluorinated copolymer in a solvent. The solvent is preferably chosen from: n-methylpyrrolidone (NMP), dimethylsulfoxide (DMSO), N,N-dimethylformamide (DMF), triethylphosphite (TEP), acetone, tetrahydrofuran, methyl ethylketone (MEK), methyl isobutyl ketone (MiBK), ethyl acetate (EA), butyl acetate (BA), ethylene carbonate (EC), propylene carbonate (PC), dimethyl carbonate (DMC), diethyl carbonate (DEC) or ethyl methyl carbonate (EMC).
[0030] According to one embodiment, the formulation further comprises conductive carbon additives and active material particles in suspension in said solvent.. Such formulation is particularly suitable for forming battery electrode films, notably positive (cathode) electrode or negative (anode) electrod for a lithium ion battery. Active material for lithium ion battery cathode formulation can be selected from the group, not limiting to, lithium iron phosphate (LFP), lithium nickel manganese cobalt oxide (NMC), lithium-manganese-cobalt-oxide (LCO), lithium-nickel- cobalt-aluminum oxide (NCA), lithium-manganese oxide (LMO), lithium-nickel-manganese- oxide (LNMO) , and lithium manganese iron phosphate (LMFP). Active material for anode formulation can be from graphite, hard carbon, soft carbon, graphene, silicon, silicon monoxide (SiO), tin, or lithium titanate (LTO). The invention encompasses a battery comprising the fluorinated copolymer described herein. [0031] The invention further contemplates a process for preparing the fluorinated copolymer in an aqueous reaction medium, comprising:
a) forming an aqueous emulsion comprising at least one initiator, a stabilizer, at least one fluorinated vinylic monomer, and a halogenated monomer (1) as defined above, b) initiating copolymerization of said at least one fluorinated vinylic monomer with said halogenated monomer (1) with stirring, under heat and super- atmospheric pressure.
[0032] A polymerization reaction in accordance with the present invention may be carried out by charging a reactor with water (preferably deionized water), at least one fluorinated vinylic monomer, at least one halogenated Monomer (1) as defined above and optionally, one or more of a surfactant, a chain-transfer agent and/or an antifoulant. Air may be purged from the reactor prior to the introduction of the fluoromonomer. Water is added to the reactor before bringing the reactor to the desired starting temperature, but the other materials may be added before or after bringing the reactor to temperature. At least one radical initiator is added to start and maintain the polymerization reaction. Additional vinylic fluoromonomer(s) and/or additional functional monomer (Monomer 1) may be optionally added to replenish monomer that is consumed, and the other materials may be optionally added during the course of the polymerization to maintain the reaction and control the final product properties. In a typical embodiment, all monomer components will be fed at a controlled ratio (to each other) to maintain reaction pressure
Monomer (1)
[0033] The structure of Monomer (1) is detailed above.
[0034] The Monomers (1) comonomers may be used in the reactor in an amount, for example, of from about 0.001 to about 15 weight percent, preferably from about 0.01 to about 15 weight percent based on total monomer. Preferably they are used in an amount from about 0.001 to about 10 weight percent, preferably 0.01 to about 10 weight percent based on total monomer. In various embodiments, the total amount of hydrophilic monomer(s) is at least 0.001, at least 0.01, at least 0.05, at least 0.1, at least 1.0 or at least 2.0 weight percent based on total monomer. In other embodiments, the total amount of hydrophilic monomer does not exceed 13.0, 10.0, 9.0, 7.0, 6.0, 5.0 weight percent based on total monomer. The hydrophilic (meth)acrylic comonomer (Monomer (1)) may be used in solution such as in aqueous solution for convenient handling.
[0035] In one embodiment, two or more different functional acrylates was found to provide increased adhesion. While not being bound by any particular theory, it is believed that different functionalities, for example an alcohol and acid functionality, could react or crosslink to form ester groups. The two or more different functionalities preferably are present in the same terpolymer, but could also be a blend of two or more different copolymers.
Surfactants
[0036] The surfactant used in the polymerization can be any surfactant known in the art to be useful in PVDF emulsion polymerization, including perfluorinated, partially fluorinated, and non- fluorinated surfactants. In a preferred embodiment, the PVDF emulsion of the present disclosure can be fluorosurfactant free, with no fluoro surfactants being used in any part of the polymerization. Non-fluorinated surfactants useful in the PVDF polymerization could be both ionic and non-ionic in nature including, but are not limited to, 3-allyloxy-2-hydroxy-l-propane sulfonic acid salt, polyvinylphosphonic acid, polyacrylic acids, polyvinyl sulfonic acid, and salts thereof, polyethylene glycol and/or polypropylene glycol and the block copolymers thereof, alkyl phosphonates and siloxane-based surfactants.
[0037] Surfactants can also be used in combination with hydrophilic (meth)acrylic comonomer to provide further stability to the polymer emulsion. Preferred surfactants are non-fluorinated hydrocarbon surfactants, siloxane surfactants or a combination thereof. For example a hydrophilic (meth)acrylic comonomer can be used in combination with sodium dodecyl benzene sulfonate (SDDBS), sodium octyl sulfonate, sodium lauryl sulfate, ammonium lauryl sulfate, or sodium laureth sulfate, among others. In certain embodiments of the invention, no fluorosurfactant is present in the aqueous emulsion and/or no fluorosurfactant is introduced during copolymerization of the fluorinated vinylic monomer with the hydrophilic (meth)acrylic comonomer. In one embodiment, the stabilizer is a poly electrolyte. In another embodiment, the stabilizer of the polymer emulsion is a functionalized cellulose.
Initiators
[0038] The term "initiator" and the expressions "radical initiator" and "free radical initiator" refer to a chemical that is capable of providing a source of free radicals, either induced spontaneously, or by exposure to heat or light. Examples of suitable initiators include peroxides, peroxydicarbonates and azo compounds. “Initiators” also includes redox systems useful in providing a source of free radicals. The term "radical" and the expression "free radical" refer to a chemical species that contains at least one unpaired electron.
[0039] The radical initiator is added to the reaction mixture in an amount sufficient to initiate and maintain the polymerization reaction at a desired reaction rate. The order of addition may vary according to the desired process and latex emulsion characteristics.
[0040] The radical initiator may comprise a persulfate salt, such as sodium persulfate, potassium persulfate, or ammonium persulfate. The amount of persulfate salt added to the reaction mixture (based upon the total weight of monomer added to the reaction mixture) may, for example, be from about 0.002 to about 1.0 weight percent.
[0041] The radical initiator may comprise an organic peroxide such as an alkyl, dialkyl, or diacyl peroxide, peroxydicarbonates, and peroxy esters or mixtures thereof. A preferred dialkyl peroxide is di-tert-butylperoxide (DTBP), which may be added to the reaction mixture in an amount from about 0.01 to about 5 weight percent on total monomer, and is preferably added in an amount from about 0.05 to about 2.5 weight percent on total monomer. Preferred peroxydicarbonate initiators are di-n-propyl peroxydicarbonate and diisopropyl peroxydicarbonate, which may be added to the reaction mixture in an amount from about 0.5 to about 2.5 weight percent on total monomer. Peroxy ester initiators include tert-amyl peroxypivalate, tertbutyl peroxypivalate, and succinic acid peroxide.
[0042] The radical initiator may comprise an azo initiator, such as 2,2'- azobis(2 methyl- propionamidine)dihydrochloride.
[0043] The radical initiator may comprise a redox system. By "redox system" is meant a system comprising an oxidizing agent, a reducing agent and optionally, a promoter as an electron transfer medium. Oxidizing agents include, for example, persulfate salts; peroxides, such as hydrogen peroxide; hydroperoxides such as tert-butyl hydroperoxide and cumene hydroperoxide; and oxidizing metal salts such as, for example, ferric sulfate. Reducing agents include, for example, sodium formaldehyde sulfoxylate, sodium and potassium sulfite, ascorbic acid, bisulfite, metabisulfite, and reduced metal salts. The promoter is a component of the redox system which, in different oxidation states, is capable of reacting with both the oxidant and the reducing agent, thereby accelerating the overall reaction. Promoters include, for example, transition metal salts such as ferrous sulfate. In redox systems, the oxidizing agent and the reducing agent may be utilized in an amount from about 0.01 to about 0.5 weight percent on total monomer. The optional promoter may be utilized in an amount from about 0.005 to about 0.025 weight percent on total monomer. Redox systems are described in G.S. Misra and U.D.N. Bajpai, Prog. Polym. Sci., 1982, 8(1-2), pp. 61-131.
Chain-Transfer Agents
[0044] Chain-transfer agents are added to the polymerization to regulate the molecular weight of the product. They may be added to a polymerization in a single portion at the beginning of the reaction, or incrementally or continuously throughout the reaction. The amount and mode of addition of chain-transfer agent depend on the activity of the particular chain transfer agent employed, and on the desired molecular weight of the polymer product. The amount of chain- transfer agent added to the polymerization reaction is preferably from about 0.05 to about 5 weight percent, more preferably from about 0.1 to about 2 weight percent based on the total weight of monomer added to the reaction mixture.
[0045] Oxygenated compounds such as alcohols, carbonates, ketones, esters, and ethers may serve as chain-transfer agents. Examples of oxygenated compounds useful as chain-transfer agents include isopropyl alcohol, as described in U.S. Patent 4,360,652. Other classes of compounds which may serve as chain-transfer agents in the polymerization of halogen-containing monomers include, for example, halocarbons and hydrohalocarbons, such as chlorocarbons. Alkanes such as ethane and propane may also function as chain-transfer agents.
Buffering Agent
[0046] The polymerization reaction mixture may optionally contain a buffering agent to maintain a controlled pH throughout the polymerization reaction. The pH is preferably controlled within the range of from about 4 to about 8, to minimize undesirable color development in the product.
[0047] Buffering agents may comprise an organic or inorganic acid or alkali metal salt thereof, or base or salt of such organic or inorganic acid, that has at least one pKa value and/or pKb value in the range of from about 4 to about 10, preferably from about 4.5 to about 9.5. Preferred buffering agents in the practice of the invention include, for example, phosphate buffers and acetate buffers. A "phosphate buffer" is a salt or a mixture of salts of phosphoric acid. An "acetate buffer" is a salt of acetic acid. [0048] Buffering agents are preferably employed where potassium persulfate is employed as the radical initiator. A preferred buffering agent for use with persulfate radical initiators is sodium acetate. A preferred amount of sodium acetate buffer is from about 50 wt.% to about 150 wt.%, based on the weight of persulfate initiator added to the reaction. In one preferred embodiment, the initiator feed comprises approximately equal weights of potassium persulfate and sodium acetate in aqueous solution.
Antifoulant
[0049] The addition of a paraffin wax or hydrocarbon oil to the reaction serves as an antifoulant to minimize or prevent polymer adhesions to the reactor components. Any long chain saturated hydrocarbon wax or oil can perform this function. The amount of oil or wax added to the reactor is an amount which serves to minimize the formation of polymer adhesions on the reactor components. The amount is generally proportional to the interior surface area of the reactor and may vary from about 1 to about 40 mg per square centimeter of reactor interior surface area. The amount of paraffin wax or hydrocarbon oil is preferably about 5 mg/cm2 of the reactor interior surface area.
Co-Polymerization Conditions
[0050] The temperature used for polymerization may vary, for example, from 20-130 degrees Celsius, depending on the initiator system chosen. The polymerization temperature is preferably from 35-130 degrees Celsius, and most preferably from 70-125 degrees Celsius.
[0051] The pressure used for polymerization may vary from 280-20,000 kPa, depending on the capabilities of the reaction equipment, the initiator system chosen, and the monomer selection. The polymerization pressure is preferably from 2,000-11,000 kPa, and most preferably from 2,750-6,900 kPa.
[0052] The polymerization occurs under stirring or other agitation. The stirring/agitation may be constant, or may be varied to optimize process conditions during the course of the polymerization. In one embodiment, both multiple stirring speeds and multiple temperatures are used for controlling the reaction.
[0053] According to one embodiment of the process of the invention, a pressurized polymerization reactor equipped with a stirrer and heat control means is charged with water, preferably deionized water, one or more halogenated monomers (1) and at least one fluorinated vinylic monomer. The mixture may optionally contain one or more of a surfactant, a buffering agent, an antifoulant or a chain-transfer agent for molecular weight regulation of the polymer product.
[0054] Prior to introduction of the monomer or monomers, air is preferably removed from the reactor in order to obtain an oxygen-free environment for the polymerization reaction.
[0055] The order in which the polymerization components are assembled may be varied, although it is generally preferred that at least a portion of the Monomer (1) is present in the aqueous reaction medium prior to the initiation of the polymerization of the fluorinated vinylic monomer. An additional amount of Monomer (1) may be fed to the reactor during the reaction.
[0056] In one embodiment, water, initiator, Monomer (1) and optionally surfactant, antifoulant, chain transfer agent and/or buffer are charged to the reactor, and the reactor heated to the desired reaction temperature. The fluorinated vinylic monomer(s) is(are) then fed into the reactor, preferably at a rate which provides an essentially constant pressure.
[0057] Alternatively the fluorinated vinylic monomer, Monomer (1) and initiator can be fed to the reactor, along with one or more of the optional ingredients. Other variations for fluoropolymer copolymerization processes are contemplated, as known in the art.
[0058] The monomer feed is terminated when the desired weight of monomer has been fed to the reactor. Additional radical initiator is optionally added, and the reaction is allowed to react out for a suitable amount of time. The reactor pressure drops as the monomer within the reactor is consumed.
[0059] Upon completion of the copolymerization reaction, the reactor is brought to ambient temperature and the residual unreacted monomer is vented to atmospheric pressure. The aqueous reaction medium containing the copolymer is then recovered from the reactor as a latex. The latex consists of a stable mixture of the reaction components, i.e., water, Monomer (1), initiator (and/or decomposition products of the initiator) and copolymer solids.
[0060] Generally, the latex contains from about 10 to about 50 weight percent copolymer solids. The polymer in the latex may be in the form of small particles having a size range of from about 30 nm to about 800 nm.
Product Handling
[0061] The product of the copolymerization is a latex which can be used in that form, usually after filtration of solid byproducts from the polymerization process, or which can be coagulated to isolate the solids, which may then be washed and dried. For use in latex form, the latex can be stabilized by the addition of a surfactant, which may be the same as or different from the surfactant present during polymerization (if any). This later added surfactant may, for example, be an ionic or non-ionic surfactant. In one embodiment of the invention, no fluorosurfactant is added to the latex. For solid product, the latex may be coagulated mechanically or by the addition of salts or acids, and then isolated by well-known means such as by filtration. Once isolated, solid product can be purified by washing or other techniques, and it may be dried for use as a powder, which can be further processed into granules, pellets or the like.
[0062] In one embodiment, the functional copolymer according to the invention is applied to a substrate, as a latex in water or as a solvent solution, the solvent being chosen among those listed above. Optionally, a primer layer can be applied to the substrate, before the layer of functional copolymer.
[0063] In one embodiment, said substrate is porous, for example a porous membrane.
EXAMPLES
[0064] Cathode formulation and fabrication
[0065] One exemplary cathode slurry preparation procedure for laboratory scale is described here. PVDF copolymer of the invention is first dissolved in N-methylpyrrolidone (NMP) solvent, typically in 5-l0wt% concentration. Conductive carbon additive, such as SuperP-Li from Timcal, is added to the binder solution, and mixed using a centrifugal planetary mixer, Thinky AR-310, for 3 repeats of l20s at 2000rpm with lmin air cooling in between. Once the conductive carbon is dispersed in the binder solution, active material such as Celcore® NMC622 (Umicore), and small amount of NMP are added to the mixture, and mixed to form a thick and uniform paste, typically 60s at 2000rpm. Then small amount of NMP is added to the paste and mixed at 60s/2000rpm to gradually reduce the slurry solids (in about 1.5% with each NMP addition) and viscosity. This dilution step is repeated multiple time until the slurry viscosity reaches proper level for coating, typically 3,000-15, OOOcP @ l/s shear rate. A typical formulation for our laboratory cathode is active material/carbon/PVDF=97/l.5/l.5 (wt/wt/wt) on dry basis.
[0066] The cathode slurry is then cast onto aluminum foil (15mhi thickness) using adjustable doctor blade on an automatic film applicator (Elcometer 4340). The wet casting is then transferred to a convection oven, and dried at 120C for 30min. After drying, the electrode is calendered using a roll mill (IRM, international roll mill), to a final density of 3.2-3.6 g/cm3, with a typical value of 3.4g/cm3. The typical areal mass loading of the dry cathode is 180-220 g/m2.
[0067] Peel strengths for cathodes were obtained via a 180° peel test using ASTM D903 with three modifications. The first modification was that the extension rate used was 50 mm/minute (peel rate of 25 mm/minute), electrodes were tested one day after fabrication, and the electrode was bonded to the alignment plate using double sided paper tape (3M Company, type 401M) with the flexible aluminum foil current collector peeled affixed in the testing grips.
[0068] NMR Analysis for % Incorporation: Samples solution was prepared at lwt% concentration in DMSO-d6 with heating at 90C overnight. The 1H and 19F experiments were carried out using a Bruker AV III HD 500 (11.7 T) spectrometer equipped with a 5 mm TXO probe at 50°C. The peaks appearing around -160ppm in the decoupled 19F spectrum (shifted and split vs. authentic poly(methyl 2-fluoroacrylate)) were taken as indicative of the incorporated comonomer and integrated vs. total PVDF signal.
Example 1: To a 2 gallon autoclave were added 3500g of deionized water, 9.2g of low molecular weight poly(acrylic acid) (BASF CP-10S), and 0.5g of methyl 2-fluoroacrylate (MFA). The autoclave was agitated, heated to 100C and pressurized to 650psi with vinylidene fluoride. A 2.0wt% feed of potassium persulfate was started at 2.0mL/min. Upon start of pressure drop, an additional feed of MFA was started at 0.25mL/min. and pressure was maintained by additional VDF feed. Feeds were continued in this fashion, increasing MFA feed rate to moderate instantaneous VDF feed demand to maintain a range of 500-1500g/hr. MFA feed was increased in this fashion up to l.OmL/min. All feeds were continued until a total of 1650g of VDF had been fed to the reactor, corresponding to 69.6g of MFA. Monomer feeds were stopped and the pressure was allowed to autogenously decrease for 10 minutes at which point the reactor was vented to atmospheric pressure and cooled to room temperature. Latex was discharged from the reactor and dried in a convection oven overnight. 4993g of latex was recovered with solids of 31 wt%. Example 2: To a 2 gallon autoclave were added 3500g of deionized water, 9.2g of low molecular weight poly(acrylic acid) solution (BASF CP-10S), and 25mL of sodium 2-fluoroacrylate (SFA) as 5.25wt% solution in deionized water. The autoclave was agitated, heated to 100C and pressurized to 650psi with vinylidene fluoride. A 2.0wt% feed of potassium persulfate was started at 2.0mF/min. Upon start of pressure drop, an additional feed of SFA solution was started at 2.0mF/min. and pressure was maintained by additional VDF feed. Feeds were continued in this fashion, increasing SFA feed rate in order to moderate instantaneous VDF feed demand to maintain a range of 500-l500g/hr. SFA solution feed was increased in this fashion up to lO.OmF/min. All feeds were continued until a total of l650g of VDF had been fed to the reactor, corresponding to l2.45g of SFA solid. Monomer feeds were stopped and the pressure was allowed to autogenously decrease for 10 minutes at which point the reactor was vented to atmospheric pressure and cooled to room temperature. Fatex was discharged from the reactor and dried in a convection oven overnight. 6046g of latex was recovered with solids of 3 l.8wt%.
Example 3: An identical procedure as outlined in Example 1 was used except a reaction temperature of 83C was used and total of 1.15% MFA was fed vs. total VDF. Fluid latex was recovered with solids of 33.5 wt%.
Example 4: An identical procedure as outlined in Example 1 was used except a reaction temperature of 83C was used and total of 2.30% MFA was fed vs. total VDF. Fluid latex was recovered with solids of 30.5 wt%.
Figure imgf000017_0001

Claims

What is claimed is:
1. A fluorinated copolymer comprising a fluorinated vinylic monomer and a halogenated monomer (1):
Figure imgf000018_0001
Monomer (1) wherein:
Ri, R2, and R3 is a hydrogen or a halogen (F, Cl, Br, I), and at least one is a halogen;
R4 is hydrogen, a Ci to C½ linear, branched, aryl, or cycloalkyl group, a Ci to C½ fluorinated linear, branched, aryl or cycloalkyl group, a fluorinated oligomer of hexfluoropropylene oxide, an alkali metal (lithium, sodium, potassium, rubidium, cesium), ammonium, alkylammonium, or alkylarylammonium ion.
2. The copolymer of claim 1 comprising up to l0.0wt% of Monomer (1).
3. The copolymer of claim 1 , wherein said fluorinated vinylic monomer is vinylidene fluoride.
4. The copolymer of claim 3, wherein Ri is fluorine.
5. The copolymer of claim 4, wherein R4 is Ci to C½ linear, branched or cycloalkyl group.
6 The copolymer of claim 3, wherein Ri and R2 are fluorine and R4 is Ci to Ci6 linear, branched or cycloalkyl group.
7. The copolymer of claim 3, wherein Ri, R2 and R3 are fluorine and R4 is Ci to C½ linear, branched or cycloalkyl group.
8. The copolymer of claim 4, wherein R4 is hydrogen or an alkali metal, ammonium, or alkylammonium.
9. The copolymer of claim 3, wherein Ri and R2 are fluorine and R4 is hydrogen or an alkali metal, ammonium, or alkylammonium.
10. The copolymer of claim 3, wherein Ri, R2 and R3 are fluorine and R4 is hydrogen or an alkali metal, ammonium, or alkylammonium.
11. A formulation comprising the fluorinated copolymer of any of claims 1 to 10, in a solvent.
12. The formulation of claim 11, wherein said solvent is chosen from: n-methylpyrrolidone (NMP), dimethylsulfoxide (DMSO), N,N-dimethylformamide (DMF), triethylphosphite (TEP), acetone, tetrahydrofuran, methyl ethylketone (MEK), methyl isobutyl ketone (MiBK), ethyl acetate (EA), butyl acetate (BA), ethylene carbonate (EC), propylene carbonate (PC), dimethyl carbonate (DMC), diethyl carbonate (DEC) or ethyl methyl carbonate (EMC).
13. The formulation of claim 11 or 12 further comprising conductive carbon additives and cathode active material particles. Active material for lithium ion battery cathode formulation can be selected from the group, not limiting to : lithium iron phosphate (LFP), lithium nickel manganese cobalt oxide (NMC), lithium-manganese-cobalt-oxide (LCO), lithium-nickel-cobalt- aluminum oxide (NCA), lithium-manganese oxide (LMO), lithium-nickel- manganese-oxide (LNMO) , and lithium manganese iron phosphate (LMFP).
14. The formulation of claim 11 further comprising conductive carbon additives and anode active material particles, preferably the anode active material particles is selected from the group consisting of graphite, hard carbon, soft carbon, graphene, silicon, silicon monoxide (SiO), tin, and lithium titanate (LTO).
15. A process for preparing the fluorinated copolymer of claim 1 in an aqueous reaction medium, comprising:
a) forming an aqueous emulsion comprising at least one initiator, a stabilizer, at least one fluorinated vinylic monomer, and halogenated Monomer (1),
b) initiating copolymerization of said at least one fluorinated vinylic monomer with said halogenated Monomer (1) with stirring, under heat and super- atmospheric pressure.
16. The process of claim 15, wherein the aqueous medium is additionally comprised of at least one buffering agent.
17. The process of any one of claims 15 and 16, wherein polymerization is carried out at a temperature of from about 35 to about 130 degrees Celsius.
18. The process of any one of claims 15 to 17, wherein polymerization is carried out at a polymerization pressure of from about 2750 to about 6900 kPa.
19. The process of any one of claims 15 to 18, wherein the initiator is a persulfate or an organic peroxide.
20. An article comprising the formulation of any one of claims 11 to 13, wherein said article is a battery electrode film, notably a positive electrode for a lithium ion battery.
21. A battery comprising the fluorinated copolymer of any one of claims 1 to 10.
22. A coated substrate on which the copolymer of any one of claims 1 to 10 is applied as a latex in water or as a solvent solution.
23. A porous membrane comprising the copolymer of any one of claims 1 to 10 is applied as a latex in water or as a solvent solution.
PCT/US2019/026490 2018-04-10 2019-04-09 Functional fluoropolymers Ceased WO2019199752A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
EP19784265.1A EP3774714B1 (en) 2018-04-10 2019-04-09 Electrodes and batteries comprising functional fluoropolymers
CN201980024552.7A CN111954657A (en) 2018-04-10 2019-04-09 Functional Fluoropolymer
US17/045,263 US12435174B2 (en) 2018-04-10 2019-04-09 Functional fluoropolymers
KR1020207032363A KR102836859B1 (en) 2018-04-10 2019-04-09 Functional fluoropolymer
JP2020555440A JP7535947B2 (en) 2018-04-10 2019-04-09 Functional Fluoropolymers

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201862655453P 2018-04-10 2018-04-10
US62/655,453 2018-04-10

Publications (1)

Publication Number Publication Date
WO2019199752A1 true WO2019199752A1 (en) 2019-10-17

Family

ID=68163777

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2019/026490 Ceased WO2019199752A1 (en) 2018-04-10 2019-04-09 Functional fluoropolymers

Country Status (6)

Country Link
US (1) US12435174B2 (en)
EP (1) EP3774714B1 (en)
JP (1) JP7535947B2 (en)
KR (1) KR102836859B1 (en)
CN (1) CN111954657A (en)
WO (1) WO2019199752A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114292554A (en) * 2022-01-27 2022-04-08 上海水立方新材料有限公司 Modified nano-silica reinforced aqueous PVDF coating and preparation method thereof
JP2023528873A (en) * 2020-06-02 2023-07-06 アーケマ・インコーポレイテッド Method for manufacturing battery electrode with improved properties

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112189271A (en) 2018-06-12 2021-01-05 株式会社吴羽 Binder composition, electrode mixture, electrode structure, method for producing electrode structure, and secondary battery
CN115863639B (en) * 2021-09-26 2025-05-13 比亚迪股份有限公司 Binder for dry electrode and preparation method thereof
CN115558049B (en) * 2022-10-19 2024-01-26 上海华谊三爱富新材料有限公司 Vinylidene fluoride copolymer and preparation method thereof
CN115441042A (en) * 2022-10-21 2022-12-06 天能帅福得能源股份有限公司 Low-temperature lithium iron phosphate battery and preparation method thereof

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4360652A (en) 1981-08-31 1982-11-23 Pennwalt Corporation Method of preparing high quality vinylidene fluoride polymer in aqueous emulsion
US5415958A (en) 1992-12-02 1995-05-16 Kureha Kagaku Kogyo Kabushiki Kaisha Vinylidene fluoride copolymer, and binder composition containing the copolymer for non-aqueous solvent-type secondary battery
JP2000200623A (en) 1999-01-06 2000-07-18 Reiko Udagawa Lithium battery having fluorine-containing polymer electrolyte
JP2002249522A (en) 2001-02-23 2002-09-06 Nippon Mektron Ltd Carboxy group-containing fluorocopolymer
JP2002249589A (en) 2001-02-23 2002-09-06 Nippon Mektron Ltd Gel composition
US20050170255A1 (en) * 2002-10-03 2005-08-04 Daikin Industries, Ltd. Solid electrolyte comprising fluorine-containing polymer having fluorine-containing ether chains
US7241817B2 (en) 2003-06-06 2007-07-10 Arkema France Process for grafting a fluoropolymer and multilayer structures comprising this grafted polymer
US7351498B2 (en) 2001-04-10 2008-04-01 Mitsubishi Materials Corporation Lithium ion polymer secondary battery its electrode and method for synthesizing polymer compound in binder used in adhesion layer thereof
US8337725B2 (en) 2007-04-24 2012-12-25 Solvay Solexis S.P.A. Vinylidene fluoride copolymers
WO2013110740A1 (en) 2012-01-25 2013-08-01 Solvay Sa Fluoropolymers as binder for the electrodes in supercapacitors
US20140147726A1 (en) * 2011-07-06 2014-05-29 Zeon Corporation Porous membrane for secondary battery, separator for secondary battery, and secondary battery
CN104725544A (en) 2013-12-20 2015-06-24 浙江蓝天环保高科技股份有限公司 Novel vinylidene fluoride copolymer with high cohesiveness
US20150196585A1 (en) * 2012-07-19 2015-07-16 Relypsa, Inc. Compositions comprising crosslinked cation-binding polymers and uses thereof
US20160046746A1 (en) 2013-04-03 2016-02-18 Arkema France Copolymers containing vinylidene fluoride and trifluoroethylene
WO2017163756A1 (en) * 2016-03-23 2017-09-28 旭硝子株式会社 Method for producing α-fluoro acrylic acid ester, and composition containing highly-pure fluorocyclopropane derivative, and composition containing highly-pure α-fluoro acrylic acid ester
JP6269890B1 (en) 2016-10-07 2018-01-31 ダイキン工業株式会社 Binder for secondary battery and electrode mixture for secondary battery

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5141678B1 (en) * 1964-08-07 1976-11-11
JPS551351B2 (en) * 1974-03-07 1980-01-12
JPS5523567B1 (en) 1977-05-09 1980-06-24
JPS54135400A (en) * 1978-04-13 1979-10-20 Kureha Chemical Ind Co Ltd High dielectric film
JPS5554311A (en) * 1978-10-18 1980-04-21 Japan Atom Energy Res Inst Preparation of fluorine-containing polymer having functional group
US4294675A (en) * 1978-10-18 1981-10-13 Japan Atomic Energy Research Institute Process for production of fluorine-containing multi-component copolymers
JPS5827803B2 (en) * 1979-04-27 1983-06-11 日本原子力研究所 Method for producing cross-linked fluorine-containing copolymer containing ion exchange group
JPS57137308A (en) * 1981-02-19 1982-08-24 Nippon Mektron Ltd Production of copolymer
JP4605919B2 (en) 2001-02-26 2011-01-05 甲南化工株式会社 Protein purification carrier, production method thereof, and protein purification method using the same
US7121817B2 (en) 2002-05-30 2006-10-17 Anest Iwata Corporation Scroll fluid machine comprising compressing and expanding sections
JP2007258127A (en) * 2006-03-27 2007-10-04 Sony Corp Negative electrode and battery
JP5423214B2 (en) * 2009-07-31 2014-02-19 旭硝子株式会社 Novel fluorine-containing copolymer and membrane
JP5701131B2 (en) * 2011-04-05 2015-04-15 株式会社クレハ Vinylidene fluoride copolymer and use of the copolymer
US10745555B2 (en) 2011-06-23 2020-08-18 Solvay Specialty Polymer Italy S.P.A. Process for manufacturing porous membranes
CN104725545A (en) 2013-12-23 2015-06-24 浙江蓝天环保高科技股份有限公司 Novel high-cohesiveness vinylidene fluoride copolymer
US11643486B1 (en) * 2022-06-08 2023-05-09 Arkema Inc. Non-linear vinylidene fluoride copolymers
JP2025135400A (en) * 2024-03-05 2025-09-18 ローム株式会社 Semiconductor Devices

Patent Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4360652A (en) 1981-08-31 1982-11-23 Pennwalt Corporation Method of preparing high quality vinylidene fluoride polymer in aqueous emulsion
US5415958A (en) 1992-12-02 1995-05-16 Kureha Kagaku Kogyo Kabushiki Kaisha Vinylidene fluoride copolymer, and binder composition containing the copolymer for non-aqueous solvent-type secondary battery
JP2000200623A (en) 1999-01-06 2000-07-18 Reiko Udagawa Lithium battery having fluorine-containing polymer electrolyte
JP2002249522A (en) 2001-02-23 2002-09-06 Nippon Mektron Ltd Carboxy group-containing fluorocopolymer
JP2002249589A (en) 2001-02-23 2002-09-06 Nippon Mektron Ltd Gel composition
US7351498B2 (en) 2001-04-10 2008-04-01 Mitsubishi Materials Corporation Lithium ion polymer secondary battery its electrode and method for synthesizing polymer compound in binder used in adhesion layer thereof
US20050170255A1 (en) * 2002-10-03 2005-08-04 Daikin Industries, Ltd. Solid electrolyte comprising fluorine-containing polymer having fluorine-containing ether chains
US7241817B2 (en) 2003-06-06 2007-07-10 Arkema France Process for grafting a fluoropolymer and multilayer structures comprising this grafted polymer
US8337725B2 (en) 2007-04-24 2012-12-25 Solvay Solexis S.P.A. Vinylidene fluoride copolymers
US20140147726A1 (en) * 2011-07-06 2014-05-29 Zeon Corporation Porous membrane for secondary battery, separator for secondary battery, and secondary battery
WO2013110740A1 (en) 2012-01-25 2013-08-01 Solvay Sa Fluoropolymers as binder for the electrodes in supercapacitors
US20150196585A1 (en) * 2012-07-19 2015-07-16 Relypsa, Inc. Compositions comprising crosslinked cation-binding polymers and uses thereof
US20160046746A1 (en) 2013-04-03 2016-02-18 Arkema France Copolymers containing vinylidene fluoride and trifluoroethylene
CN104725544A (en) 2013-12-20 2015-06-24 浙江蓝天环保高科技股份有限公司 Novel vinylidene fluoride copolymer with high cohesiveness
WO2017163756A1 (en) * 2016-03-23 2017-09-28 旭硝子株式会社 Method for producing α-fluoro acrylic acid ester, and composition containing highly-pure fluorocyclopropane derivative, and composition containing highly-pure α-fluoro acrylic acid ester
JP6269890B1 (en) 2016-10-07 2018-01-31 ダイキン工業株式会社 Binder for secondary battery and electrode mixture for secondary battery
EP3447831A1 (en) 2016-10-07 2019-02-27 Daikin Industries, Ltd. Binder for secondary batteries and electrode mixture for secondary batteries

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
BOSCHET ET AL., MACROMOLECULES AMERICAN CHEM. SOCIETY, vol. 43, no. 11, 8 June 2010 (2010-06-08), pages 4879 - 4888
G. S. MISRAU.D.N. BAJPAI, PROG. POLYM. SCI., vol. 8, no. 1-2, 1982, pages 61 - 131
See also references of EP3774714A4

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2023528873A (en) * 2020-06-02 2023-07-06 アーケマ・インコーポレイテッド Method for manufacturing battery electrode with improved properties
JP7765412B2 (en) 2020-06-02 2025-11-06 アーケマ・インコーポレイテッド Method for manufacturing battery electrodes with improved properties
CN114292554A (en) * 2022-01-27 2022-04-08 上海水立方新材料有限公司 Modified nano-silica reinforced aqueous PVDF coating and preparation method thereof
CN114292554B (en) * 2022-01-27 2022-07-26 上海水立方新材料有限公司 Modified nano-silica reinforced aqueous PVDF coating and preparation method thereof

Also Published As

Publication number Publication date
US20210171693A1 (en) 2021-06-10
KR102836859B1 (en) 2025-07-23
JP7535947B2 (en) 2024-08-19
US12435174B2 (en) 2025-10-07
EP3774714A4 (en) 2021-12-22
CN111954657A (en) 2020-11-17
EP3774714A1 (en) 2021-02-17
JP2021521296A (en) 2021-08-26
KR20200141485A (en) 2020-12-18
EP3774714B1 (en) 2025-04-23

Similar Documents

Publication Publication Date Title
US12209152B2 (en) Functional fluoropolymers
US12435174B2 (en) Functional fluoropolymers
US11643484B2 (en) Modified fluoropolymers
US9434837B2 (en) Method of producing fluoropolymers using acid-functionalized monomers
US10570231B2 (en) Fluoropolymers
CN119173547A (en) Nonlinear vinylidene fluoride copolymer
US20230197964A1 (en) Electrode binder composition for lithium ion electrical storage devices
CN120035635A (en) Preparation of Large Particle Size Fluoropolymer Latex
CN121152818A (en) Shear-stable aqueous fluoropolymer dispersions

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 19784265

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2020555440

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 20207032363

Country of ref document: KR

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 2019784265

Country of ref document: EP

Effective date: 20201110

WWG Wipo information: grant in national office

Ref document number: 2019784265

Country of ref document: EP

WWG Wipo information: grant in national office

Ref document number: 17045263

Country of ref document: US