WO2008129041A1 - Vinylidene fluoride copolymers - Google Patents
Vinylidene fluoride copolymers Download PDFInfo
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- WO2008129041A1 WO2008129041A1 PCT/EP2008/054831 EP2008054831W WO2008129041A1 WO 2008129041 A1 WO2008129041 A1 WO 2008129041A1 EP 2008054831 W EP2008054831 W EP 2008054831W WO 2008129041 A1 WO2008129041 A1 WO 2008129041A1
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- 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
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D69/00—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
- B01D69/02—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor characterised by their properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/40—Polymers of unsaturated acids or derivatives thereof, e.g. salts, amides, imides, nitriles, anhydrides, esters
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/40—Polymers of unsaturated acids or derivatives thereof, e.g. salts, amides, imides, nitriles, anhydrides, esters
- B01D71/401—Polymers based on the polymerisation of acrylic acid, e.g. polyacrylate
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/76—Macromolecular material not specifically provided for in a single one of groups B01D71/08 - B01D71/74
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- 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
- C08F214/225—Vinylidene fluoride with non-fluorinated comonomers
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- 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
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/20—Manufacture of shaped structures of ion-exchange resins
- C08J5/22—Films, membranes or diaphragms
- C08J5/2206—Films, membranes or diaphragms based on organic and/or inorganic macromolecular compounds
- C08J5/2218—Synthetic macromolecular compounds
- C08J5/2231—Synthetic macromolecular compounds based on macromolecular compounds obtained by reactions involving unsaturated carbon-to-carbon bonds
- C08J5/2237—Synthetic macromolecular compounds based on macromolecular compounds obtained by reactions involving unsaturated carbon-to-carbon bonds containing fluorine
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- 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
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2325/00—Details relating to properties of membranes
- B01D2325/36—Hydrophilic membranes
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/30—Polyalkenyl halides
- B01D71/32—Polyalkenyl halides containing fluorine atoms
- B01D71/34—Polyvinylidene fluoride
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use 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; Derivatives of such polymers
- C08J2327/02—Characterised by the use 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; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/12—Characterised by the use 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; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08J2327/16—Homopolymers or copolymers of vinylidene fluoride
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- 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 present invention pertains to vinylidene fluoride copolymers comprising recurring units derived from hydrophilic (meth)acrylic monomers having improved thermal stability, to a process for their manufacture, to a composition comprising the same, and to their use as binder in batteries or for the manufacture of hydrophilic membranes.
- VDF Vinylidene fluoride copolymers comprising recurring units derived from hydrophilic (meth)acrylic monomers (e.g. acrylic acid) are well known in the art.
- Such copolymers have been developed aiming at adding to the mechanical properties and chemical inertness of PVDF suitable adhesion towards metals, e.g. aluminium or copper, or hydrophilic properties.
- these materials are produced by surface functionalization of pre-formed PVDF materials, so as to obtain grafted copolymers; nevertheless such grafted copolymers suffer from the drawback that as grafting is generally initiated via radical route, by providing free radicals generation on the fluorinated backbone: uncontrolled radical side reactions occur, yielding poorly soluble, generally cross-linked materials, and/or generating chains breaks, so that the final material possess impaired mechanical properties.
- Linear copolymers are thus generally preferred when a precise control of the molecular structure is required.
- US 4861851 JAPAN SYNTHETIC RUBBER CO LTD (JP) 29.08.1989 discloses substantially random linear vinylidene fluoride acrylic acid ester copolymers comprising, inter alia, 15 to 95 % wt of at least one unit selected from alkyl acrylate and alkoxy-substituted alkyl acrylate.
- Said copolymers can be produced by copolymerizing suitable monomers in emulsion, suspension, solution or bulk polymerization, emulsion being preferred.
- WO 01/57095 09.08.2001 discloses linear fluoropolymers comprising fluorocarbon and hydrocarbon repeat units, fluorocarbon units being derived from tetrafluoroethylene, chlorotrifluoroethylene, trifluoroethylene, vinyl fluoride or vinylidene fluoride, the hydrocarbon units being derived from vinyl acetate, vinyl alcohol, acrylic acid, acrylated, methacrylates. Said materials are prepared by polymerization in a medium comprising supercritical carbon dioxide.
- WO 01/57095 09.08.2001 teaches that acrylic acid monomers have intrinsic reactivity and tend to reacts with themselves rather than with the fluorocarbon monomer, also due to the lack of physical affinity for domains of the other monomer. "Blocky" structures are generally obtained as a function of polymerization conditions. In CO 2 supercritical polymerization, the choice of selected surfactants can improve the homogeneity of the hydrocarbon monomers' distribution.
- US 5880204 (ALLIED SIGNAL INC (US) ) 09.03.1999 discloses room temperature coalescable aqueous fluoropolymer dispersions comprising fluoropolymer particles having a core-shell structure, comprising a core composed predominantly of a first semi-crystalline fluorocopolymer, and a shell composed predominantly of a second amorphous fluorocopolymer obtained by reacting, in the presence of said first copolymer, at least one cure site provider (e.g. acrylic acid), and at least two fluorinated comonomer units. Said second polymerization step yielding the amorphous terpolymer can be carried out by continuous addition of the cure site provider.
- at least one cure site provider e.g. acrylic acid
- Copolymerizing vinylidene fluoride and hydrophilic (meth)acrylic monomer remains indeed an uneasy task, due to the very different reactivity of such copolymers and their intrinsic incompatibility.
- the present invention advantageously solves the above mentioned problems by providing a linear semi-crystalline copolymer [polymer (A)] comprising recurring units derived from vinylidene fluoride (VDF) monomer and at least one hydrophilic (meth)acrylic monomer (MA) of formula:
- each of R1 , R2, R3, equal or different from each other is independently a hydrogen atom or a C 1 -C 3 hydrocarbon group, and R 0H is a hydrogen or a C 1 -C 5 hydrocarbon moiety comprising at least one hydroxyl group, said polymer (A) comprising from 0.05 to 10 % by moles of recurring units derived from said hydrophilic (meth)acrylic monomer (MA) and being characterized by a fraction of randomly distributed units (MA) of at least 40 %.
- Another object of the present invention is a novel process for the manufacture of linear semi-crystalline copolymers as above described, said process advantageously comprising polymerizing in an aqueous medium in the presence of a radical initiator the vinylidene fluoride (VDF) monomer and the hydrophilic (meth)acrylic monomer (MA) in a reaction vessel, said process comprising
- Another object of the invention is a composition comprising polymer (A) as above defined and a VDF polymer.
- Still another object of the invention is the use of the linear semi-crystalline copolymers as above detailed as binder in Li-batteries electrodes or for the manufacture of hydrophilic membranes.
- the substantially random distribution of hydrophilic (meth)acrylic monomer (MA) within the polyvinylidene fluoride backbone of the polymer (A) advantageously maximizes the effects of the modifying monomer (MA) on both adhesiveness and/or hydrophilic behaviour of the resulting copolymer, even at low levels of hydrophilic (meth)acrylic monomer (MA) in the composition, without impairing the other outstanding properties of the vinylidene fluoride polymers, e.g. thermal stability and mechanical properties.
- Polymer (A) comprises recurring units derived from derived from vinylidene fluoride (VDF) monomer and from at least one hydrophilic (meth)acrylic monomer (MA).
- VDF vinylidene fluoride
- MA hydrophilic (meth)acrylic monomer
- the VDF monomer referred to herein can include, in addition to vinylidene fluoride, at least one conventionally used monomer copolymerizable with vinylidene fluoride, such as vinyl fluoride, trifluoroethylene, trifluorochloroethylene, tetrafluoroethylene, hexafluoropropylene, and fluoroalkyl vinyl ether.
- the amount of vinylidene fluoride in the vinylidene fluoride monomer is at least 70 mol %, so as not to impair the excellent properties of vinylidene fluoride resin, such as chemical resistance, weatherability, and heat resistance.
- the VDF monomer does not include any monomer other than vinylidene fluoride, that is to say the VDF monomer is vinylidene fluoride.
- hydrophilic (meth)acrylic monomer (MA) is understood to mean that the polymer (A) may comprise recurring units derived from one or more than one hydrophilic (meth)acrylic monomer (MA) as above described.
- hydrophilic (meth)acrylic monomer (MA) and “monomer (MA)” are understood, for the purposes of the present invention, both in the plural and the singular, that is to say that they denote both one or more than one hydrophilic (meth)acrylic monomer (MA).
- polymer (A) consists essentially of recurring units derived from VDF mononomer and monomer (MA).
- Polymer (A) may still comprise other moieties such as defects, end-groups and the like, which do not affect nor impair its physico -chemical properties.
- hydrophilic (meth)acrylic monomer (MA) preferably complies formula:
- each of R1 , R2, R 0H have the meanings as above defined, and R3 is hydrogen; more preferably, each of R1 , R2, R3 are hydrogen, while R 0H has the same meaning as above detailed.
- Non limitative examples of hydrophilic (meth)acrylic monomers (MA) are notably acrylic acid, methacrylic acid, hydroxyethyl (meth)acrylate, hydroxypropyl(meth)acrylate; hydroxyethylhexyl(meth)acrylates.
- the monomer (MA) is more preferably selected among: - hydroxyethylacrylate (HEA) of formula:
- HPA 2-hydroxy propyl acrylate
- the monomer (MA) is AA and/or HEA.
- polymer (A) it is essential that in polymer (A) the fraction of randomly distributed units (MA) is of at least 40 %. Only polymers wherein this condition is fulfilled possess adequate thermal resistance in combination with other properties such as adhesiveness and/or hydrophilicity.
- fraction of randomly distributed units (MA) is intended to denote the percent ratio between the average number of (MA) monomer sequences (%), said sequences being comprised between two recurring units derived from VDF monomer, and the total average number of (MA) monomer recurring units (%), according to the following formula: a ⁇ erage number of (MA) sequences (%)
- Determination of total average number of (MA) monomer recurring units in polymer (A) can be performed by any suitable method. Mention can be notably made of acid-base titration methods, well suited e.g. for the determination of the acrylic acid content, of NMR methods, adequate for the quantification of (MA) monomers comprising aliphatic hydrogens in side chains (e.g. HPA, HEA), of weight balance based on total fed (MA) monomer and unreacted residual (MA) monomer during polymer (A) manufacture.
- acid-base titration methods well suited e.g. for the determination of the acrylic acid content, of NMR methods, adequate for the quantification of (MA) monomers comprising aliphatic hydrogens in side chains (e.g. HPA, HEA), of weight balance based on total fed (MA) monomer and unreacted residual (MA) monomer during polymer (A) manufacture.
- the average number of (MA) monomer sequences (%) can be determined e.g. by 19 F-NMR according to standard methods.
- the fraction of randomly distributed units (MA) is of preferably at least 50%, more preferably of at least 60%, most preferably of at least 70 %.
- Polymer (A) comprises preferably at least 0.1 , more preferably at least 0.2 % moles of recurring units derived from said hydrophilic (meth)acrylic monomer (MA).
- Polymer (A) comprises preferably at most 10, more preferably at most 7.5 % moles, even more preferably at most 5 % moles, most preferably at most 3 % moles of recurring units derived from said hydrophilic (meth)acrylic monomer (MA).
- the polymer (A) has advantageously an intrinsic viscosity of above 0.1 dl/g and at most 20 dl/g, preferably in the range of 0.2 - 15 dl/g, more preferably in the range of 0.5 - 10.0 dl/g.
- the polymer (A) be used as binder, especially for forming electrodes of Lithium batteries, it possesses preferably an intrinsic viscosity of at least 1.0 dl/g, more preferably of at least 1.5 dl/g; also maximum intrinsic viscosity is generally in this case of 5 dl/g, preferably of 4 dl/g.
- Polymer (A) is semi-crystalline.
- semi-crystalline is intended to denote a polymer (A) which possesses a detectable melting point. It is generally understood that a semi-crystalline polymer (A) possesses a heat of fusion determined according to ASTM D 3418 of advantageously at least 0.4 J/g, preferably of at least 0.5 J/g, more preferably of at least 1 J/g.
- Semi-crystalline polymers (A) have significant advantages over amorphous products, as they exhibit the required properties, and in particular suitable mechanical properties without additional crosslinking treatments.
- Polymer (A) is a linear copolymer, that is to say that it is composed of macromolecules made of substantially linear sequences of recurring units from VDF monomer and (MA) monomer; polymer (A) is thus distinguishable from grafted and/or comb-like polymers.
- Polymer (A) advantageously possesses improved thermal resistance.
- polymer (A) undergoes a loss in weight of 1 % wt in TGA analysis under nitrogen following ISO 11358 standard at a temperature of more than 350°C, preferably of more than 360°C, more preferably of more than 380 0 C.
- Another object of the present invention is a novel process for the manufacture of linear semi-crystalline copolymers as above described.
- the process of the invention advantageously comprises polymerizing in an aqueous medium in the presence of a radical initiator the vinylidene fluoride (VDF) monomer and the hydrophilic (meth)acrylic monomer (MA) in a reaction vessel, said process comprising
- Critical pressure of vinylidene fluoride is known to be 4.43 MPa (corresponding to 44.3 bar). It is essential that during the whole polymerization run, pressure is maintained above critical pressure of vinylidene fluoride. Generally the pressure is maintained at a value of more than 50 bars, preferably of more than 75 bars, even more preferably of more than 100 bars.
- VDF monomer and, optionally, of hydrophilic (meth)acrylic monomer (MA) is loaded into the reaction vessel at the beginning of the process.
- continuous feeding or “continuously feeding” means that slow, small, incremental additions the aqueous solution of hydrophilic (meth)acrylic monomer (MA) take place until polymerization has concluded.
- the aqueous solution of hydrophilic (meth)acrylic monomer (MA) continuously fed during polymerization amounts for at least 50 % wt of the total amount of monomer (MA) supplied during the reaction (i.e. initial charge plus continuous feed). Preferably at least 60 % wt, more preferably at least 70 % wt, most preferably at least 80 % wt of the total amount of monomer (MA) is continuously fed during polymerization.
- variations in monomer (MA) concentration during polymerization typically occur: higher initial monomer (MA) concentrations can thus be encountered yielding monomer (MA) - blocky structures.
- VDF monomer An incremental addition of VDF monomer can be effected during polymerization, even if this requirement is not mandatory. To the sake of simplicity it would be generally preferred to introduce all the VDF monomer required at the onset of the polymerization.
- the process of the invention is carried out at a temperature of at least 35°C, preferably of at least 40°C, more preferably of at least 45°C.
- composition (C) comprising polymer (A) and at least one VDF polymer.
- VDF polymer is intended to denote polymer comprising at least 70 % moles of recurring units derived from VDF and, optionally, up to 30 % moles of recurring units derived from at least one other suitable fluorinated comonomer, e.g. hexafluoropropylene, chlorotrifluoroethylene, trifluoroethylene, and the like. VDF homopolymer is particularly advantageous for the compositions of the invention.
- Said composition (C) advantageously comprises at least 5 % wt, preferably at least 10 % wt of polymer (A).
- composition (C) can be notably used for achieving the target properties of adhesion/hydrophilicity provided by the polymer (A) component, by reducing the required amount of highly valuable polymer (A), by dilution with a VDF polymer.
- an object of the invention is the use of the polymer (A) as above described or of the composition (C) as above detailed as binder, especially for forming electrodes of Lithium batteries and/or electric double layer capacitors.
- binder As binder will be described in relation with polymer (A); it is nevertheless understood that the composition (C) as above detailed can be used in //euof polymer (A) in all embodiments detailed here below.
- a binder solution of polymer (A) is generally prepared.
- the organic solvent used for dissolving the polymer (A) to provide the binder solution according to the present invention may preferably be a polar one, examples of which may include: N-methyl-2-pyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide, dimethylsulfoxide, hexamethylphosphamide, dioxane, tetrahydrofuran, tetramethylurea, triethyl phosphate, and trimethyl phosphate.
- the vinylidene fluoride polymer used in the present invention has a much larger polymerization degree than a conventional one, it is further preferred to use a nitrogen-containing organic solvent having a larger dissolving power, such as N-methyl-2-pyrrolidone, N,N-dimethylformamide or N,N-dimethylacetamide among the above-mentioned organic solvents.
- a nitrogen-containing organic solvent having a larger dissolving power such as N-methyl-2-pyrrolidone, N,N-dimethylformamide or N,N-dimethylacetamide.
- the binder solution of polymer (A) As above detailed, it is preferred to dissolve 0.1 - 10 wt. parts, particularly 1 - 5 wt. parts, of the copolymer (A) in 100 wt. parts of such an organic solvent. Below 0.1 wt. part, the polymer occupies too small a proportion in the solution, thus being liable to fail in exhibiting its performance of binding the powdery electrode material. Above 10 wt. parts, an abnormally high viscosity of the solution is obtained, so that not only the preparation of the electrode-forming composition becomes difficult but also avoiding gelling phenomena can be an issue.
- the polymer (A) binder solution it is preferred to dissolve the copolymer (A) in an organic solvent at an elevated temperature of 30 - 200 0 C, more preferably 40 - 160 0 C, further preferably 50 - 150 0 C. Below 30 0 C, the dissolution requires a long time and a uniform dissolution becomes difficult.
- An electrode-forming composition may be obtained by adding and dispersing a powdery electrode material (an active substance for a battery or an electric double layer capacitor), and optional additives, such as an electroconductivity-imparting additive and/or a viscosity modifying agent, into the thus-obtained polymer (A) binder solution.
- a powdery electrode material an active substance for a battery or an electric double layer capacitor
- optional additives such as an electroconductivity-imparting additive and/or a viscosity modifying agent
- an object of the invention is thus an electrode-forming composition
- an electrode-forming composition comprising polymer (A) or composition (C), a powdery electrode material and, optionally, an electroconductivity-imparting additive and/or a viscosity modifying agent.
- the active substance may comprise a composite metal chalcogenide represented by a general formula of LiMY 2 , wherein M denotes at least one species of transition metals such as Co, Ni, Fe, Mn, Cr and V; and Y denotes a chalcogen, such as O or S.
- M denotes at least one species of transition metals such as Co, Ni, Fe, Mn, Cr and V
- Y denotes a chalcogen, such as O or S.
- a lithium-based composite metal oxide represented by a general formula of LiMO 2 wherein M is the same as above.
- Preferred examples thereof may include: LiCoO 2 , LiNiO 2 , LiNi x Co 1-x O 2 (O ⁇ x ⁇ 1), and spinel-structured LiMn 2 O 4 .
- the active substance may comprise a lithiated or partially lithiated transition metal oxyanion-based electrode materials of the nominal formula AB(XO 4 ) f E 1-f , in which A is lithium, which may be partially substituted by another alkali metal representing less that 20% of the A metals, B is a main redox transition metal at the oxidation level of +2 chosen among Fe, Mn, Ni or mixtures thereof, which may be partially substituted by one or more additional metal at oxidation levels between +1 and +5 and representing less than 35% of the main +2 redox metals, including 0, XO 4 is any oxyanion in which X is either P, S, V, Si, Nb, Mo or a combination thereof, E is a fluoride, hydroxide or chloride anion, f is the molar fraction Of XO 4 oxyanion, generally comprised between 0.75 and 1 (extremoxO 4 ) f, in which A is lithium, which may be partially substituted by another alkali metal
- the above AB(XO 4 ) f E 1-f active substances are preferably phosphate-based and may have an ordered or modified olivine structure.
- the active substance as above described complies with formula Li 3-x M' y M" 2-y (XO 4 ) 3 in which: 0 ⁇ x ⁇ 3, 0 ⁇ y ⁇ 2; M' and M" are the same or different metals, at least one of which being a redox transition metal; XO 4 is mainly PO 4 which may be partially substitued with another oxyanion, in which X is either P, S, V, Si, Nb, Mo or a combination thereof.
- the active material is a phosphate-based electrode material having the nominal formula Li(Fe x Mn 1-x )PO 4 in which 0 ⁇ x ⁇ 1 , wherein x is preferably 1 (that is to say, Lithium Iron Phosphate of formula: LiFePO 4 ).
- the active substance may preferably comprise a carbonaceous material, such as graphite, activated carbon or a carbonaceous material obtained by carbonization of phenolic resin, pitch, etc.
- the carbonaceous material may preferably be used in the form of particles having an average diameter of ca. 0.5 - 100 ⁇ m.
- An electroconductivity-imparting additive may be added in order to improve the conductivity of a resultant composite electrode layer formed by applying and drying of the electrode-forming composition of the present invention, particularly in case of using an active substance, such as LiCoO 2 or LiFePO 4 , showing a limited electron-conductivity.
- an active substance such as LiCoO 2 or LiFePO 4
- Examples thereof may include: carbonaceous materials, such as carbon black, graphite fine powder and fiber, and fine powder and fiber of metals, such as nickel and aluminum.
- the active substance for an electric double layer capacitor may preferably comprise fine particles or fiber, such as activated carbon, activated carbon fiber, silica or alumina particles, having an average particle (or fiber) diameter of 0.05 - 100 ⁇ m and a specific surface area of 100 - 3000 m 2 /g, i.e., having a relatively small particle (or fiber) diameter and a relatively large specific surface area compared with those of active substances for batteries.
- fine particles or fiber such as activated carbon, activated carbon fiber, silica or alumina particles, having an average particle (or fiber) diameter of 0.05 - 100 ⁇ m and a specific surface area of 100 - 3000 m 2 /g, i.e., having a relatively small particle (or fiber) diameter and a relatively large specific surface area compared with those of active substances for batteries.
- the preferred electrode-forming composition for positive electrodes comprises:
- polymer (A) in an amount from 1 to 10 % wt, preferably from 2 to 9 % wt, more preferably about 3 % wt, with respect to the total weight (a)+(b)+(c);
- a powdery electrode material preferably a composite metal chalcogenide represented by a general formula of LiMY 2 , as above detailed, or a lithiated or partially lithiated transition metal oxyanion-based electrode materials of the nominal formula AB(XO 4 ) f E 1-f , as above detailed, in an amount from 80 to 97% wt, preferably from 85 to 94 % wt, more preferably about 92 % wt.
- Still another object of the invention is the use of the polymer (A) or of composition (C), as above described for the manufacture of a hydrophilic membrane.
- the present invention thus pertains to a process for the manufacture of a hydrophilic membrane comprising polymer (A) or composition (C), and to the hydrophilic membrane comprising polymer (A) or composition (C), as above described.
- membrane possesses its usual meaning, that is to say it refers, in essence, to a discrete, generally thin, interface that moderates the permeation of chemical species in contact with it.
- This interface may be molecularly homogeneous, that is, completely uniform in structure (dense membrane), or it may be chemically or physically heterogeneous, for example containing voids, holes or pores of finite dimensions (porous membrane).
- pore void
- hole will be used as synonymous within the context of the present invention.
- the membrane of the invention is preferably a porous membrane.
- a porous membrane possesses generally a voided structure with interconnected pores.
- Porous membranes are generally characterized by the average pore diameter (d) and the porosity ( ⁇ ), i.e. the fraction of the total membrane that is porous.
- the porous membrane of the invention has a porosity ( ⁇ ) of advantageously at least 1 %, preferably of at least 2 %, more preferably of at least 3 % and advantageously at most 90 %, preferably of at most 80 %.
- These pores have generally an average diameter (d) of advantageously at least 0.01 , preferably of at least 0.05, more preferably of at least 0.1 ⁇ m and advantageously at most 50 ⁇ m, preferably of at least 25 ⁇ m, more preferably of at least 10 ⁇ m.
- the membrane can be under the form of a flat-sheet or can be produced under the form of thin tubes or fibers (hollow-fiber membranes).
- Flat-sheet membranes are generally preferred when high fluxes are required. Formation of membrane into hollow fibers is particularly advantageous when compact modules with high surface areas are required.
- the membranes of the invention can be used in the chemical processing industry in various separation processes, such as microfiltration and preferably ultrafiltration, in particular of aqueous media, and in biomedical applications, e.g. for haemodialysis, for controlled release of drugs, for artificial organs, such as kidney, lung and pancreas.
- the process of the invention advantageously comprises casting and/or melt forming the polymer (A) as above defined.
- Melt forming is commonly used to make dense membranes either by extrusion as a sheet from a die or as a blown film.
- the process of the invention advantageously comprises at least one step including one of irradiation technique, film expansion, template leaching technique, solution precipitation technique.
- a film of the polymer (A) as above described made by conventional techniques is first irradiated with charged particles from a suitable radiation source, said particles typically breaking polymer chains and leaving sensitized/damaged tracks; then said irradiated film is passed through a suitable etch solution etching preferentially along the sensitized tracks, thereby forming pores.
- porous membranes are prepared by subsequent orientation and stretching; thus an oriented film of the copolymer (A) as above described is typically extruded under drawdown; after cooling, the film is advantageously stretched at right angle to the original orientation, so that the crystalline structure of the polymer is typically deformed and slit-like voids are advantageously formed.
- a homogeneous film is prepared from a mixture of the membrane material (i.e. the polymer (A) as above described) and a leachable component. After the film has been formed, the leachable component is removed with a suitable solvent and a porous membrane is formed.
- the leachable component could be a soluble low molecular weight solid or liquid, such as a plasticizer, a low molecular weight VDF polymer, and the like.
- a clear solution comprising the polymer (A) as above described is precipitated into two phases, namely a solid, polymer-rich phase which forms the matrix of the membrane and a liquid, polymer-poor phase that forms the membrane pores.
- Said polymer precipitation from solution can be achieved in several ways, such as cooling, solvent evaporation, precipitation by immersion in a non-solvent, imbibition of a non-solvent from the vapour phase.
- Casting generally involve solution casting, wherein typically a casting knife or draw-down bar is used to spread an even film of an appropriate polymer solution of the polymer (A) as above described across a suitable support. After the casting has been made, the solvent generally evaporates to leave a uniform dense membrane.
- the process comprises at least one step including template leaching technique.
- thermoplastic composition (TC) comprising polymer (A) as above described is mixed with 50 - 250 wt. parts of a plasticizer and, optionally, 0 - 80 wt. parts of a good solvent for said copolymer (A) to provide a mixture (Mx); said mixture (Mx) is processed into a film; the film is then subjected to extraction of the plasticizer (and optionally of the good solvent) by a suitable extraction solvent.
- hydrogenated plasticizer may generally be used preferably used.
- Esters or polyesters such as citrates, phthalates, trimellitates, sabacates, adipates, azelates can be notably mentioned. Examples thereof may include: adipic acid-based polyesters of, e.g., the adipic acid-propylene glycol type, and the adipic acid-1 ,3-butylene glycol type; sebacic acid-based polyesters of, e.g., the sebacic acid-propylene glycol type; azelaic acid-based polyesters of e.g., the azelaic acid-propylene glycol type, and azelaic acid-1 ,3-butylene glycol type; alkyl phthalates like, e.g.
- alkyl and acyl citrates e.g. triethyl citrate, acetyl triethyl citrate, tri-n-butyl citrate, acetyl-tri-n-butyl citrate, trioctyl citrate, acetyl-tri-octyl citrate trihexyl citrate, acetyl-trihexyl citrate, butyryl-trihexyl citrate or trihexyl-o-butyryl citrate; alkyl trimelliltates, like notably trimethyl trimellitate , tri-(2-ethylhexyl)trimellitate , tri-(n-octyl,n-decyl) trimellitate tri-(heptyl,nonyl) trimellitate, n-octy
- the good solvent for polymer (A) those capable of dissolving copolymer (A) in a temperature range of 20 - 250°C may be used.
- examples thereof may include: N-methylpyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide, dimethyl sulfoxide, methyl ethyl ketone, acetone, tetrehydrofuran, dioxane, ethyl acetate, propylene carbonate, cyclohexane, methyl isobutyl ketone, dimethyl phthalate, and solvent mixtures of these.
- NMP N-methylpyrrolidone is particularly preferred in view of its stability at high temperatures.
- a good solvent for polymer (A) is particularly advantageous when the mixture (Mx) is processed by casting, as it can advantageously help in tuning the viscosity of said mixture (Mx).
- the so obtained mixture (Mx) can be processed by extrusion moulding, injection moulding, compression moulding and/or casting to yield a film, so as to obtain advantageously the desired shape to the membrane.
- the so obtained film is dipped into an extraction solvent to extract the plasticizer and optionally the good solvent. It is possible to carry out the extraction at room temperature obtaining a complete plasticizer extraction in a time ranging from some minutes to some hours, depending on the thickness, the nature of the extraction solvent and the agitation. Generally times of few minutes are sufficient to completely extract the plasticizer. After extraction a porous membrane is obtained.
- extraction solvents solvents wherein the plasticizer is soluble, but which are not compatible with the polymer (A), so as not to cause the swelling thereof, are generally used.
- the most commonly used class of solvents is that of aliphatic alcohols, preferably having a short chain, for example from 1 to 6 carbon atoms, more preferably methanol and isopropanol.
- polymer (A) can be used for the manufacture of a hydrophilic membrane either alone, as unique thermoplastic polymer component or in admixture with another suitable thermoplastic polymer.
- composition (C) of the invention is a composition comprising polymer (A) and at least one VDF polymer, i.e. the composition (C) of the invention as above detailed.
- the Applicant has surprisingly found that an amount of at least 5 % wt is already satisfactory for substantially modifying the surface properties of membranes made from the composition as above detailed.
- Total average AA content in polymer (A) is determined by acid-base titration of the carboxylic group. The procedure which has been followed is detailed here below.
- a sample of about 0.5 g of polymer (A) is carefully weighted and dissolved in acetone at a temperature of 70-80°C. 5 ml of water are then added dropwise under vigorous stirring so that to avoid coagulation of the polymer. Titration with aqueous NaOH having a concentration of 0.1 N until complete neutralization of acidity is then carried out, with neutrality transition at about - 270 mV. AA content is thus determined on the basis of measured acid equivalents.
- the HEA content of the copolymer was determined by 1 H-NMR, measuring intensity of the H atoms of the CH 2 group as evidenced here below, with respect to the total intensity of CH 2 moieties of the polymer (A) backbone VDF monomer units:
- Fraction of randomly distributed HEA units is determined by 19 F-NMR, following an analogous procedure to that followed for determining randomly distributed AA units fraction.
- Intrinsic Viscosity was determined using the following equation on the basis of the dropping time, at 25°C, of a solution obtained by dissolving polymer (A) in dimethylformamide at a concentration of about 0.2 g/dl, in an Ubbelhode viscosimeter:
- TGA analyses were carried out according to ISO 11358 standard, under nitrogen atmosphere, in dynamic mode. Temperatures required for obtaining a weight loss of, respectively, 0.5, 0.75 and 1 % wt of polymer (A) were recorded. The higher these temperatures, the higher is the thermal stability of polymer (A).
- T m2 designates the melting temperature, as determined in 2 nd heat cycle
- T xx is the crystallization temperature, as determined during intermediate cooling cycle.
- Static contact angle measurements towards water MiIIiQ have been carried on dense flat polymer (A) sheets obtained by solution casting, using the G10-Kruss instrument, according to ASTM D 2578-84, D 5725-99. Each value was determined as the average of measurements of at least 5 drops.
- - Suspending agent 0,8g (Methocel ® K100GR from DOW Chemical). Reactor was then repeatedly evacuated and purged with nitrogen (1 bar) while maintaining the temperature at 14°C. Then 2 g of acrylic acid (AA) and then 3 g of a solution of the initiator t-amyl perpivalate in isododecane (75%) were introduced into the autoclave and immediately after, 105Og of VDF monomer were introduced into the reactor. The reactor was then gradually heated until the set-point temperature of 52°C was attained, which corresponded to a pressure of 120 bar. The pressure was kept constantly equal to 120 bar during the whole polymerization run by feeding an aqueous solution comprising 37 g of AA/I of solution.
- the polymerization was stopped by degassing the suspension until reaching atmospheric pressure. A total of 550 ml of AA solution were charged to the reactor. The polymer was then collected by filtration and suspended again in demineralized water in a stirred tank. After this washing cycle, the polymer was oven-dried at 50°C. The amount of collected dry powder was found to be 695g.
- Example 4 Preparation of electrode-forming compositions and electrodes therefrom [0127]
- Example 4 Preparation of electrode comprising polymer of example 1. 1 g of resin produced as in example 1 was dissolved in 50 g of N-methylpyrrolidone (NMP) under mechanical stirring at room temperature using a Dispermat device equipped with a flat PTFE disc. Under moderate stirring, 1.67 g of SuperP (conductive Carbon Black) and 30.67 g Lithium Cobaltum Oxide (LiCoO 2 ) were added and the slurry was thoroughly mixed to ensure a good homogeneity.
- NMP N-methylpyrrolidone
- SuperP conductive Carbon Black
- LiCoO 2 Lithium Cobaltum Oxide
- All the materials involved in the slurry preparation were previously conditioned either by drying using molecular sieve of 4A (for the solvent) or by heating for one night at 100°C (for the powders).
- the solid concentration of the composition was 40% weight, polymer (A) representing 3% wt of the total solids components (polymer (A) + active material (carbon black 5% and Li Oxide 92%)).
- the composition was then degassed under vacuum and spread using a Doctor Blade coating instrument on an Aluminum foil, previously degreased.
- the coating was finally dried in vacuum oven at the fixed temperature for enough time to ensure solvent removal, typically for 15 min at 130°C, and/or 30 min at 80°C.
- the thickness of the dried coating was found to be about 50 ⁇ m.
- Example 5 Preparation of electrode comprising polymer of example 2
- Example 8 [0137] 5 grams of polymer produced as in example 1 were added to 45 grams NMP and the mixture was stirred until complete dissolution. Dense flat polymer films were obtained by solution casting with a Braive bar coater on a glass surface, and drying at 120°C in a ventilated oven for 30 minutes. Final thickness of the dried films was found to be about 10 ⁇ m. The films were subsequently immersed for 1.5 hours in a 5%wt aqueous solution of NaOH at 70°C, and then washed with deionized water and dried at room temperature to provide specimens which were subjected to contact angle measurements. Data are summarized in Table 4.
- Example 9 Same procedure as described in example 8 was repeated but using 5 grams of polymer produced as detailed in example 2. Contact angle determinations are summarized in Table 4.
- Comparative Example 10 Same procedure as described in example 8 was repeated but using 5 grams of SOLEF ® 1015 VDF homopolymer having an intrinsic viscosity of 1.5 dl/g. Contact angle determinations are summarized in Table 4.
- Example 11 Same procedure as described in example 8 was repeated but using 5 grams of each of the mixtures comprising the polymer (A) produced as in example 2 and PVDF homopolymer (SOLEF ® 1015), whose composition is detailed in Table 5. Contact angle determinations are also summarized in Table 5.
- Example 12 [0149] A solution prepared as detailed in example 9 (resin produced as in example 2) was cast with a Braive bar coater on a glass surface, and coagulated by subsequent immersion in deionized water to obtain a porous membrane, After detachment from glass surface, the porous membrane was washed with deionized water and dried at room temperature between two sheets of paper.
- the membrane was subsequently immersed for 1.5 hours in 5%wt aqueous solution of NaOH at 70°C, and then washed with deionized water and dried at room temperature. After this treatment, the membrane color turned from white to brown.
- the wettability of the membrane was evaluated by putting a drop of distilled water on the surface of the membrane; the drop was suddenly adsorbed and spread over the surface, thus proving the hydrophilic nature of the membrane.
- Example 13 Same procedure as described in Example 12 was repeated but using the solution prepared in example 10, containing SOLEF ® 1015 VDF homopolymer. The wettability of the membrane was evaluated by putting a drop of distilled water on the surface of the membrane; the drop remained on the surface, not being adsorbed, thus not revealing any wetting improvement of the membrane.
- the pressure was maintained at 120 bar for the whole polymerization by feeding an aqueous solution of 35,7g of HEA/I of solution. After 690 minutes the polymerization was stopped by degassing the suspension until reaching atmospheric pressure. A total of 605cc of HEA solution were charged to the reactor. The polymer was then collected by filtration and suspended again in clean water in a stirred tank. After this washing cycle, the polymer was oven-dried at 50°. The amount of dry powder was found to be 713 g. The properties of the polymer are presented in Table 6. The thermal stability of the product in nitrogen atmosphere was evaluated by TGA analysis; data are summarized in Table 7.
Abstract
Description
Claims
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KR1020097023585A KR101529740B1 (en) | 2007-04-24 | 2008-04-22 | Vinylidene fluoride copolymers |
EP08749636A EP2147029B1 (en) | 2007-04-24 | 2008-04-22 | Vinylidene fluoride copolymers |
JP2010504657A JP5283688B2 (en) | 2007-04-24 | 2008-04-22 | Vinylidene fluoride copolymer |
US12/596,475 US8337725B2 (en) | 2007-04-24 | 2008-04-22 | Vinylidene fluoride copolymers |
CN2008800195712A CN101679563B (en) | 2007-04-24 | 2008-04-22 | Vinylidene fluoride copolymers |
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US10847800B2 (en) | 2016-10-07 | 2020-11-24 | Daikin Industries, Ltd. | Binder for secondary batteries and electrode mixture for secondary batteries |
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CN111247176B (en) * | 2017-10-17 | 2022-07-29 | 索尔维特殊聚合物意大利有限公司 | Method for synthesizing fluoropolymers |
US11702491B2 (en) * | 2017-12-13 | 2023-07-18 | Solvay Sa | Membrane including fluoropolymer hybrid organic/inorganic composite, and electrochemical device having the same |
EP3728359B1 (en) * | 2017-12-19 | 2022-02-09 | Solvay Specialty Polymers Italy S.p.A. | Fluorinated block copolymers and application thereof |
CN108484814B (en) * | 2018-03-02 | 2021-04-09 | 浙江衢州巨塑化工有限公司 | Hydrophilic polyvinylidene fluoride resin |
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JP7062476B2 (en) * | 2018-03-14 | 2022-05-06 | 株式会社クレハ | Binder composition, electrode mixture raw material, electrode mixture, electrode, non-aqueous electrolyte secondary battery and method for manufacturing electrode mixture |
FR3079834B1 (en) | 2018-04-10 | 2021-09-10 | Arkema Inc | FUNCTIONAL FLUOROPOLYMERS |
EP3774714A4 (en) | 2018-04-10 | 2021-12-22 | Arkema, Inc. | Functional fluoropolymers |
WO2019239781A1 (en) * | 2018-06-12 | 2019-12-19 | 株式会社クレハ | Binder composition, electrode mixture, electrode structure, method for manufacturing electrode structure, and secondary cell |
JP7137742B2 (en) * | 2018-07-09 | 2022-09-15 | ダイキン工業株式会社 | Vinylidene fluoride resin composition |
FR3083922B1 (en) * | 2018-07-11 | 2020-10-16 | Commissariat Energie Atomique | ELECTROCHEMICAL ACCUMULATOR WITH BIPOLAR ARCHITECTURE WITH A SPECIFIC STRUCTURE |
US11228037B2 (en) | 2018-07-12 | 2022-01-18 | GM Global Technology Operations LLC | High-performance electrodes with a polymer network having electroactive materials chemically attached thereto |
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JP7472128B2 (en) * | 2018-11-22 | 2024-04-22 | ソルベイ スペシャルティ ポリマーズ イタリー エス.ピー.エー. | Method for producing heat-treated PVDF |
US20220025087A1 (en) | 2018-12-20 | 2022-01-27 | Solvay Specialty Polymers Italy S.P.A. | Vinylidene fluoride polymer dispersion |
JP2022515059A (en) | 2018-12-20 | 2022-02-17 | ソルベイ スペシャルティ ポリマーズ イタリー エス.ピー.エー. | Vinylidene Fluoride Polymer Dispersion |
KR20210139338A (en) | 2019-03-22 | 2021-11-22 | 가부시끼가이샤 구레하 | Composition for electrode mixture, electrode mixture, electrode, non-aqueous electrolyte secondary battery and method for manufacturing electrode |
KR102254803B1 (en) * | 2019-11-18 | 2021-05-21 | 한국화학연구원 | Blood compatible fluorine membrane and preparation method thereof |
EP4206241A1 (en) * | 2020-08-26 | 2023-07-05 | Zhejiang Quzhou Jusu Chemical Industry Co., Ltd. | Copolymerized pvdf resin for lithium battery binder and preparation method therefor |
KR20220134103A (en) * | 2021-03-26 | 2022-10-05 | 주식회사 엘지에너지솔루션 | Positive electrode and lithium secondary battery |
WO2023277055A1 (en) | 2021-06-29 | 2023-01-05 | ダイキン工業株式会社 | Composition for forming electrode, electrode and secondary battery |
CN114369211B (en) * | 2021-12-27 | 2023-12-19 | 万华化学集团股份有限公司 | Polyvinylidene fluoride resin composition, preparation method and application thereof |
US11643486B1 (en) | 2022-06-08 | 2023-05-09 | Arkema Inc. | Non-linear vinylidene fluoride copolymers |
CN114989344B (en) * | 2022-06-14 | 2023-09-19 | 万华化学集团股份有限公司 | Vinylidene fluoride copolymer, preparation method thereof and application thereof in lithium ion battery |
CN114891146B (en) * | 2022-06-21 | 2023-09-19 | 万华化学(四川)电池材料科技有限公司 | High-heat-resistance vinylidene fluoride copolymer and preparation method and application thereof |
DE102022118484A1 (en) | 2022-07-25 | 2024-01-25 | Bayerische Motoren Werke Aktiengesellschaft | Cathode and lithium ion battery with the cathode |
CN115124686B (en) * | 2022-08-31 | 2022-12-13 | 拓迪化学(上海)有限公司 | Adhesive and insulating adhesive of lithium ion battery and preparation method and application thereof |
CN115594789B (en) * | 2022-11-01 | 2023-09-19 | 万华化学集团股份有限公司 | Method for preparing polyvinylidene fluoride resin by acrylic acid copolymerization |
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CN116041604A (en) * | 2023-01-06 | 2023-05-02 | 浙江巨化技术中心有限公司 | Branched polyvinylidene fluoride resin and preparation method and application thereof |
CN116675800B (en) * | 2023-08-03 | 2024-01-30 | 宁德时代新能源科技股份有限公司 | Fluorine-containing polymer, preparation method, positive electrode plate, secondary battery and electricity utilization device |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1001765A (en) * | 1962-03-22 | 1965-08-18 | Du Pont | Terpolymers and elastomer surfaced structures made therefrom |
GB1011577A (en) * | 1963-06-10 | 1965-12-01 | Du Pont | Vinylidene fluoride copolymers |
US3438953A (en) * | 1965-01-18 | 1969-04-15 | Minnesota Mining & Mfg | Carboxy and ester terminated copolymers of vinylidene fluoride-hexafluoropropene and method of preparation |
US4749607A (en) * | 1985-06-15 | 1988-06-07 | Mitsubishi Petrochemical Co., Ltd. | Thermoplastic halocarbon polymer laminates |
EP0601754A1 (en) * | 1992-12-02 | 1994-06-15 | Kureha Kagaku Kogyo Kabushiki Kaisha | Vinylidene fluoride copolymer, and binder composition containing the copolymer for non-aqueous solvent type secondary battery |
US5880204A (en) | 1995-09-27 | 1999-03-09 | Alliedsignal Inc. | Room temperature coalescable aqueous fluoropolymer dispersions and method for their manufacture |
WO2001057095A1 (en) | 2000-02-02 | 2001-08-09 | Lousenberg Robert D | Linear copolymers of fluorocarbon-hydrocarbon monomers synthesized in carbon dioxide |
EP1621573A1 (en) | 2003-04-16 | 2006-02-01 | Kureha Corporation | Porous film of vinylidene fluoride resin and method for producing same |
WO2006026521A1 (en) * | 2004-08-31 | 2006-03-09 | Advanced Cardiovascular Systems, Inc. | Polymers of fluorinated monomers and hydrophilic monomers |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2006604A (en) * | 1934-05-25 | 1935-07-02 | Raymond W Post | Fish lure |
JPS51132294A (en) | 1975-05-14 | 1976-11-17 | Central Glass Co Ltd | A method for preparing vinylidene fluoride resin |
JPS62156951A (en) | 1985-12-28 | 1987-07-11 | 三菱化成ビニル株式会社 | Vinyl chloride group resin laminate |
JPS63145026A (en) * | 1986-12-10 | 1988-06-17 | 三菱油化株式会社 | Thermoplastic halogen-contained resin laminate |
JPS63182310A (en) * | 1987-01-22 | 1988-07-27 | Japan Synthetic Rubber Co Ltd | Vinylidene fluoride/acrylate copolymer and its production |
AU621916B2 (en) | 1988-06-20 | 1992-03-26 | Ppg Industries, Inc. | Polymerizable surfactant |
JP2767819B2 (en) | 1988-07-23 | 1998-06-18 | 大日本インキ化学工業株式会社 | Non-aqueous dispersion type resin composition |
US5229461A (en) * | 1990-05-22 | 1993-07-20 | Daikin Industries, Ltd. | Vinylidene fluoride copolymer and composition containing the same |
NO912922L (en) | 1990-09-05 | 1992-03-06 | Atochem North America | PEROXIDES FOR POLYMERIZATION REACTIONS. |
JPH05194668A (en) * | 1991-07-05 | 1993-08-03 | Japan Synthetic Rubber Co Ltd | Vinylidene fluoride-fluorine-containing (meth)acrylic acid ester copolymer, its production and coating composition using the same |
AU701611B2 (en) | 1994-10-28 | 1999-02-04 | Dsm Ip Assets B.V. | Free radical polymerisation process |
US5618900A (en) | 1996-01-16 | 1997-04-08 | The Dow Chemical Company | Free radical polymerization |
JP3387392B2 (en) * | 1997-10-24 | 2003-03-17 | ダイキン工業株式会社 | Fluorinated polymer aqueous dispersion composition |
EP1306397A1 (en) * | 2000-07-27 | 2003-05-02 | Asahi Glass Company Ltd. | Aqueous fluorocopolymer dispersion |
US6420502B1 (en) | 2000-10-23 | 2002-07-16 | The Penn State Research Foundation | Living free radical initiators based on alkylperoxydiarylborane derivatives and living free radical polymerization process |
JP4992203B2 (en) * | 2005-06-24 | 2012-08-08 | 日本ゼオン株式会社 | Lithium ion secondary battery |
JP2011518247A (en) * | 2008-04-16 | 2011-06-23 | ボストン サイエンティフィック サイムド,インコーポレイテッド | Medical implant coating compositions based on fluorinated polymers |
-
2008
- 2008-04-14 TW TW097113500A patent/TWI437009B/en active
- 2008-04-22 WO PCT/EP2008/054831 patent/WO2008129041A1/en active Application Filing
- 2008-04-22 US US12/596,475 patent/US8337725B2/en active Active
- 2008-04-22 KR KR1020097023585A patent/KR101529740B1/en active IP Right Grant
- 2008-04-22 CN CN2008800195712A patent/CN101679563B/en active Active
- 2008-04-22 JP JP2010504657A patent/JP5283688B2/en active Active
- 2008-04-22 EP EP08749636A patent/EP2147029B1/en active Active
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1001765A (en) * | 1962-03-22 | 1965-08-18 | Du Pont | Terpolymers and elastomer surfaced structures made therefrom |
GB1011577A (en) * | 1963-06-10 | 1965-12-01 | Du Pont | Vinylidene fluoride copolymers |
US3438953A (en) * | 1965-01-18 | 1969-04-15 | Minnesota Mining & Mfg | Carboxy and ester terminated copolymers of vinylidene fluoride-hexafluoropropene and method of preparation |
US4749607A (en) * | 1985-06-15 | 1988-06-07 | Mitsubishi Petrochemical Co., Ltd. | Thermoplastic halocarbon polymer laminates |
EP0601754A1 (en) * | 1992-12-02 | 1994-06-15 | Kureha Kagaku Kogyo Kabushiki Kaisha | Vinylidene fluoride copolymer, and binder composition containing the copolymer for non-aqueous solvent type secondary battery |
US5880204A (en) | 1995-09-27 | 1999-03-09 | Alliedsignal Inc. | Room temperature coalescable aqueous fluoropolymer dispersions and method for their manufacture |
WO2001057095A1 (en) | 2000-02-02 | 2001-08-09 | Lousenberg Robert D | Linear copolymers of fluorocarbon-hydrocarbon monomers synthesized in carbon dioxide |
EP1621573A1 (en) | 2003-04-16 | 2006-02-01 | Kureha Corporation | Porous film of vinylidene fluoride resin and method for producing same |
WO2006026521A1 (en) * | 2004-08-31 | 2006-03-09 | Advanced Cardiovascular Systems, Inc. | Polymers of fluorinated monomers and hydrophilic monomers |
Cited By (109)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011014490A (en) * | 2009-07-06 | 2011-01-20 | Sony Corp | Electrode, and battery having the same |
WO2012084578A1 (en) | 2010-12-22 | 2012-06-28 | Solvay Specialty Polymers Italy S.P.A. | Vinylidene fluoride copolymers |
WO2012084579A1 (en) * | 2010-12-22 | 2012-06-28 | Solvay Specialty Polymers Italy S.P.A. | Vinylidene fluoride and trifluoroethylene polymers |
WO2012084580A1 (en) | 2010-12-22 | 2012-06-28 | Solvay Specialty Polymers Italy S.P.A. | Hydrophilic vinylidene fluoride polymers |
US9701766B2 (en) | 2010-12-22 | 2017-07-11 | Solvay Specialty Polymers Italy S.P.A. | Hydrophilic vinylidene fluoride polymers |
US9751967B2 (en) | 2010-12-22 | 2017-09-05 | Solvay Specialty Polymers Italy S.P.A. | Vinylidene fluoride and trifluoroethylene polymers |
US9441054B2 (en) | 2010-12-22 | 2016-09-13 | Solvay Specialty Polymers Italy S.P.A. | Vinylidene fluoride copolymers |
US20130273424A1 (en) * | 2010-12-28 | 2013-10-17 | Kureha Corporation | Vinylidene Fluoride Copolymers and Uses of the Copolymers |
US9512255B2 (en) * | 2010-12-28 | 2016-12-06 | Kureha Corporation | Vinylidene fluoride copolymers and uses of the copolymers |
WO2012175416A1 (en) | 2011-06-23 | 2012-12-27 | Solvay Specialty Polymers Italy S.P.A. | Process for manufacturing porous membranes |
US10985353B2 (en) | 2011-06-23 | 2021-04-20 | Solvay Specialty Polymers Italy S.P.A. | Secondary batteries |
US10256498B2 (en) | 2011-06-23 | 2019-04-09 | Solvay Specialty Polymers Italy S.P.A. | Process for manufacturing battery components |
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WO2012175418A1 (en) | 2011-06-23 | 2012-12-27 | Solvay Specialty Polymers Italy S.P.A. | Process for manufacturing battery components |
US10745555B2 (en) | 2011-06-23 | 2020-08-18 | Solvay Specialty Polymer Italy S.P.A. | Process for manufacturing porous membranes |
US20140120269A1 (en) * | 2011-06-23 | 2014-05-01 | Solvay Specialty Polymers Italy S.P.A. | Process for manufacturing battery components |
US10079388B2 (en) | 2011-07-15 | 2018-09-18 | Solvay Specialty Polymers Italy S.P.A. | Aqueous vinylidene fluoride-(meth)acrylic co-polymer latex, electrode and lithium ion secondary battery using the same |
WO2013010936A1 (en) | 2011-07-15 | 2013-01-24 | Solvay Specialty Polymers Italy S.P.A. | Aqueous vinylidene fluoride polymer latex |
WO2013010854A3 (en) * | 2011-07-15 | 2013-08-15 | Solvay Specialty Polymers Italy S.P.A. | Fluoropolymer composition for multilayer assemblies |
US11441007B2 (en) | 2011-07-15 | 2022-09-13 | Solvay Specialty Polymers Italy S.P.A. | Fluoropolymer composition for multilayer assemblies |
US10920006B2 (en) | 2011-12-13 | 2021-02-16 | Solvay Specialty Polymers Italy S.P.A. | Hybrid polymers |
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WO2014012860A1 (en) | 2012-07-16 | 2014-01-23 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Process for manufacturing a li-ion battery comprising a fluoropolymeric separator |
US9991057B2 (en) | 2012-08-06 | 2018-06-05 | Solvay Specialty Polymers Italy S.P.A | Hybrid fluoropolymer composition |
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WO2014201194A1 (en) * | 2013-06-12 | 2014-12-18 | E. I. Du Pont De Nemours And Company | Hybrid battery binder |
WO2015128337A1 (en) * | 2014-02-28 | 2015-09-03 | Solvay Specialty Polymers Italy S.P.A. | Crosslinkable fluoropolymers |
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EP3118230B1 (en) | 2014-03-11 | 2017-09-13 | Kureha Corporation | Vinylidene fluoride copolymer, method for producing same, gel electrolyte and nonaqueous battery |
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US11799086B2 (en) | 2017-07-07 | 2023-10-24 | Ppg Industries Ohio, Inc. | Electrode binder slurry composition for lithium ion electrical storage devices |
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US11777096B2 (en) | 2017-07-07 | 2023-10-03 | Ppg Industries Ohio, Inc. | Electrode binder slurry composition for lithium ion electrical storage devices |
US11840800B2 (en) * | 2017-07-14 | 2023-12-12 | Arkema Inc. | High strength polyvinylidene fluoride based sized reinforcing fibers |
WO2018104564A2 (en) | 2017-08-11 | 2018-06-14 | Solvay Specialty Polymers Italy S.P.A. | Method for stabilizing aqueous dispersions of fluorinated polymers |
US11555094B2 (en) | 2017-08-11 | 2023-01-17 | Solvay Specialty Polymers Italy S.P.A. | Method for stabilizing aqueous dispersions of fluorinated polymers |
WO2019101829A1 (en) | 2017-11-24 | 2019-05-31 | Solvay Specialty Polymers Italy S.P.A. | Pvdf binders for graphite/silicon anodes |
WO2019101806A1 (en) | 2017-11-24 | 2019-05-31 | Solvay Specialty Polymers Italy S.P.A. | Flexible pvdf polymers |
US11594734B2 (en) | 2018-02-28 | 2023-02-28 | Kureha Corporation | Vinylidene fluoride polymer, binder composition, electrode mixture, electrode, and non-aqueous electrolyte secondary battery, and method for producing electrode mixture |
EP3794046B1 (en) | 2018-05-17 | 2023-03-08 | Solvay Specialty Polymers Italy S.p.A. | Flexible vdf polymers |
WO2020030694A1 (en) | 2018-08-09 | 2020-02-13 | Solvay Specialty Polymers Italy S.P.A. | Crosslinkable blends of vdf copolymers |
EP3833697B1 (en) * | 2018-08-09 | 2023-11-15 | Solvay Specialty Polymers Italy S.p.A. | Self crosslinking pvdf |
WO2020030690A1 (en) | 2018-08-09 | 2020-02-13 | Solvay Specialty Polymers Italy S.P.A. | Self crosslinking pvdf |
WO2020127651A1 (en) | 2018-12-21 | 2020-06-25 | Solvay Specialty Polymers Italy S.P.A. | Highy flexible vdf polymer |
WO2020127653A1 (en) | 2018-12-21 | 2020-06-25 | Solvay Specialty Polymers Italy S.P.A. | Flexible polymer electrolyte |
WO2020169496A1 (en) | 2019-02-19 | 2020-08-27 | Solvay Specialty Polymers Italy S.P.A. | Composition for lithium battery electrodes |
WO2020225041A1 (en) | 2019-05-03 | 2020-11-12 | Solvay Sa | Method for the manufacture of electrodes |
WO2021018615A1 (en) | 2019-07-29 | 2021-02-04 | Solvay Specialty Polymers Italy S.P.A. | Secondary batteries |
WO2021023707A1 (en) | 2019-08-07 | 2021-02-11 | Solvay Specialty Polymers Italy S.P.A. | Composition for secondary battery electrodes |
WO2021023709A1 (en) | 2019-08-07 | 2021-02-11 | Solvay Specialty Polymers Italy S.P.A. | Composition for secondary battery electrodes |
EP3792304A1 (en) | 2019-09-10 | 2021-03-17 | Solvay SA | Compositions and films comprising a vinylidene fluoride (co)polymer and an aromatic compound, and their preparation and uses |
WO2021084074A1 (en) | 2019-10-30 | 2021-05-06 | Solvay Sa | Compositions and films comprising a polymer and tis2 particles, and their preparation and uses |
KR20220132569A (en) | 2020-02-28 | 2022-09-30 | 다이킨 고교 가부시키가이샤 | Composition, binder, electrode mixture, electrode and secondary battery |
KR20220132571A (en) | 2020-02-28 | 2022-09-30 | 다이킨 고교 가부시키가이샤 | Polyvinylidene fluoride, binder, electrode mixture, electrode and secondary battery |
WO2021172585A1 (en) | 2020-02-28 | 2021-09-02 | ダイキン工業株式会社 | Polyvinylidene fluoride, binder, electrode mixture, electrode, and secondary battery |
WO2021172586A1 (en) | 2020-02-28 | 2021-09-02 | ダイキン工業株式会社 | Composition, binding agent, electrode mixture, electrode and secondary battery |
WO2022148680A1 (en) | 2021-01-08 | 2022-07-14 | Solvay Sa | Method for the manufacture of electrodes |
WO2022200345A1 (en) | 2021-03-22 | 2022-09-29 | Solvay Specialty Polymers Italy S.P.A. | Composition for electrodes |
WO2022223347A1 (en) | 2021-04-19 | 2022-10-27 | Solvay Specialty Polymers Italy S.P.A. | Composition for lithium battery electrodes |
WO2022221992A1 (en) * | 2021-04-19 | 2022-10-27 | Solvay Specialty Polymers Italy S.P.A. | Method for manufacturing partially fluorinated polymers |
WO2022223348A1 (en) | 2021-04-19 | 2022-10-27 | Solvay Specialty Polymers Italy S.P.A. | Method for manufacturing partially fluorinated polymers |
WO2022258551A1 (en) | 2021-06-10 | 2022-12-15 | Solvay Specialty Polymers Italy S.P.A. | High performance binders for lithium battery electrodes |
WO2023034784A1 (en) * | 2021-08-31 | 2023-03-09 | Saint-Gobain Performance Plastics Corporation | Tube and method for making same |
WO2023094623A1 (en) | 2021-11-29 | 2023-06-01 | Solvay Specialty Polymers Italy S.P.A. | Battery electrode and method of making the same |
WO2023187035A1 (en) | 2022-04-01 | 2023-10-05 | Solvay Specialty Polymers Italy S.P.A. | Method for separating the electrode materials from the current collector in electrodes from spent lithium-ion batteries |
WO2023198717A1 (en) | 2022-04-12 | 2023-10-19 | Solvay Specialty Polymers Italy S.P.A. | Positive electrode binder for lithium ion batteries |
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US8337725B2 (en) | 2012-12-25 |
JP5283688B2 (en) | 2013-09-04 |
TW200911848A (en) | 2009-03-16 |
KR101529740B1 (en) | 2015-06-18 |
CN101679563A (en) | 2010-03-24 |
US20100133482A1 (en) | 2010-06-03 |
EP2147029B1 (en) | 2013-02-20 |
TWI437009B (en) | 2014-05-11 |
CN101679563B (en) | 2012-01-18 |
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