WO2022065434A1 - 電解コンデンサ - Google Patents

電解コンデンサ Download PDF

Info

Publication number
WO2022065434A1
WO2022065434A1 PCT/JP2021/035092 JP2021035092W WO2022065434A1 WO 2022065434 A1 WO2022065434 A1 WO 2022065434A1 JP 2021035092 W JP2021035092 W JP 2021035092W WO 2022065434 A1 WO2022065434 A1 WO 2022065434A1
Authority
WO
WIPO (PCT)
Prior art keywords
acid
electrolytic capacitor
compound
liquid component
component
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/JP2021/035092
Other languages
English (en)
French (fr)
Japanese (ja)
Inventor
雄一郎 椿
佳津代 齊藤
達治 青山
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.)
Panasonic Intellectual Property Management Co Ltd
Original Assignee
Panasonic Intellectual Property Management Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Panasonic Intellectual Property Management Co Ltd filed Critical Panasonic Intellectual Property Management Co Ltd
Priority to US18/246,089 priority Critical patent/US12300445B2/en
Priority to CN202180064741.4A priority patent/CN116235266A/zh
Priority to JP2022552071A priority patent/JPWO2022065434A1/ja
Publication of WO2022065434A1 publication Critical patent/WO2022065434A1/ja
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Images

Classifications

    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/004—Details
    • H01G9/022—Electrolytes; Absorbents
    • H01G9/035—Liquid electrolytes, e.g. impregnating materials
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/145—Liquid electrolytic capacitors
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/15—Solid electrolytic capacitors

Definitions

  • the present invention relates to an electrolytic capacitor including a conductive polymer compound and a liquid component.
  • the electrolytic capacitor includes a capacitor element and a liquid component (electrolytic solution).
  • the capacitor element includes an anode having a dielectric layer on its surface and a conductive polymer compound covering at least a part of the dielectric layer.
  • the liquid component includes an acid component, a base component, and a solvent.
  • Patent Document 1 proposes to use a composite acid compound of an organic acid and an inorganic acid such as borodisalicylic acid as the acid component of the liquid component. By using the complex acid compound, deterioration of the acid component due to heat is suppressed. Further, Patent Document 2 proposes to include an antioxidant such as phenol in the electrolytic solution. Antioxidants are used for the purpose of suppressing deterioration of the conductive polymer compound due to oxidation.
  • the liquid component contains water
  • oxygen is supplied to the anode body, and the function of repairing the defect of the dielectric layer in the liquid component is easily exhibited.
  • the liquid component contains a complex acid compound together with water
  • the complex acid compound is hydrolyzed by the water contained in the liquid component, and the anode is corroded by the influence of the acid (for example, salicylic acid) generated by the decomposition, and the equivalent series resistance (equivalent series resistance) ( ESR) may increase.
  • the repair of defects in the dielectric layer may be insufficient, and the leakage current may increase.
  • One aspect of the present invention comprises a condenser element and a liquid component, wherein the condenser element comprises an anode having a dielectric layer on its surface and a conductive polymer compound covering at least a part of the dielectric layer.
  • the liquid component comprises an acid component, a base component, a solvent, an antioxidant, the solvent comprises water and a polyol compound, and the acid component comprises a central atom.
  • An electrolytic capacitor comprising an organic molecule having a plurality of coordinating atoms bonded to the central atom and a coordinating compound containing the coordinating compound, wherein at least one of the plurality of coordinating atoms is an oxygen atom bonded to a carbonyl group.
  • the electrolytic capacitor according to the embodiment of the present invention includes a capacitor element and a liquid component.
  • the capacitor element comprises an anode having a dielectric layer on its surface and a conductive polymer compound covering at least a part of the dielectric layer.
  • the liquid component includes an acid component, a base component, a solvent, and an antioxidant.
  • the solvent includes water and a polyol compound.
  • the acid component includes a coordination compound. Coordinating compounds include a central atom and an organic molecule having a plurality of coordinating atoms bonded to the central atom. At least one of the plurality of coordinating atoms is an oxygen atom bonded to a carbonyl group.
  • the liquid component containing the coordination compound is advantageous for improving the heat resistance of the electrolytic capacitor. Further, when the liquid component contains water, oxygen is supplied to the anode body, and the repair function of the dielectric layer is improved. For example, if the anode contains aluminum, the oxygen supplied to the anode can contribute to the formation of aluminum oxide at the defective portion of the dielectric layer.
  • the coordinating compound contains an organic molecule having an oxygen atom bonded to a carbonyl group as a coordinating atom, and is hydrolyzed by water contained in the liquid component to produce a carboxy group or an acid having a carboxy group and a hydroxy group. obtain.
  • the effect of this degrading acid corrodes the anode, and as a result, impurities (for example, a chelated product of aluminum) are generated on the surface of the anode, the interfacial resistance between the anode and the conductive polymer compound increases, and the ESR increases.
  • impurities for example, a chelated product of aluminum
  • the defects of the dielectric layer may not be sufficiently repaired, and the leakage current may increase.
  • the present invention includes an antioxidant and a polyol compound in a liquid component containing water and a coordination compound.
  • the liquid component is in direct contact with the dielectric layer or via a conductive polymer compound.
  • the liquid component may be present between the dielectric layer of the anode body and the cathode body together with the conductive polymer compound.
  • the acid component and the base component can exist as anions and cations, respectively. Therefore, the liquid component can function as an electrolytic solution having high electrical conductivity.
  • the liquid component has a function of enhancing the contact property between the dielectric layer and the conductive polymer compound and repairing defects in the dielectric layer.
  • the acid component contains a coordination compound as the first acid component.
  • the ratio of the coordination compound to the liquid component is, for example, 0.5% by mass or more, may be 3% by mass or more, may be 0.5% by mass or more, and may be 30% by mass or less, and may be 3% by mass. % Or more and 30% by mass or less.
  • the coordination compound contains a central atom and an organic molecule.
  • Organic molecules have multiple coordinating atoms attached to the central atom. Since a strong bond can be formed with the coordination atom, the central atom of the coordination compound preferably contains at least one selected from the group consisting of a boron atom, an aluminum atom and a silicon atom.
  • the organic molecule may form a complex anion with the central atom. At this time, the organic molecule may exist, for example, as a deprotonated organic group in which the proton bonded to the coordination atom is deprotonated.
  • the number of molecules of the organic molecule coordinated per central atom may be one molecule or two or more molecules. From the viewpoint of the stability of the complex anion, an organic molecule may be selected in which two or more (for example, two or three molecules) organic molecules are coordinated per two central atoms.
  • the quantitative qualitative analysis of complex anions can be performed by, for example, the following method.
  • ⁇ Qualitative analysis> First, 30 mL of the liquid component is weighed in a glass container having a closed lid, and the infrared absorption spectrum (IR) of the liquid component in the container is measured by a predetermined measuring device (IRSprit [manufactured by Shimadzu Corporation]). Next, the container containing the liquid component is sealed and held in a high temperature environment for a certain period of time. Then, after allowing the liquid component in the container to cool down, the IR is measured again.
  • the stability of the complex anion can be evaluated by the change in the expansion and contraction vibration spectrum of the bond between the central atom and the coordination atom. It can be said that the smaller the spectral change, the higher the stability of the complex anion.
  • ⁇ Quantitative analysis> First, 30 mL of the liquid component is weighed in a glass container having a closed lid, and the nuclear magnetic resonance spectrum (NMR) of the liquid component in the container is measured with a predetermined measuring device ([AVANCE III HD [BRUKER]). The initial complex anion formation ratio (G0) is obtained from the peak intensity. Next, the container containing the liquid component is sealed and held in a high temperature environment for a certain period of time. Then, after allowing the liquid component in the container to cool down, NMR is measured again to determine the production ratio (G1) of the complex anion and the unreacted organic molecule.
  • the decomposition rate of complex anions can be determined using the following equation, and the stability of complex anions can be evaluated. It can be said that the smaller the decomposition rate, the higher the stability of the complex anion.
  • At least one of the plurality of coordination atoms contained in the coordination compound is an oxygen atom bonded to a carbonyl group.
  • the plurality of coordinating atoms may contain a plurality of oxygen atoms, and all of the plurality of coordinating atoms may be oxygen atoms.
  • the coordinating atom is an oxygen atom bonded to a carbonyl group
  • an organic compound having a carboxy group derived from an organic molecule can be produced by hydrolysis.
  • hydrolysis can produce an organic compound having a hydroxy group derived from an organic molecule.
  • the organic molecule preferably contains at least one selected from the group consisting of hydroxy acids and polycarboxylic acids.
  • Hydroxy acids include aliphatic hydroxy acids (glycolic acid, lactic acid, tartronic acid, ⁇ -, ⁇ - or ⁇ -hydroxybutyric acid, malic acid, citric acid, etc.), aromatic hydroxy acids (salicylic acid, mandelic acid, benzylic acid, etc.).
  • Etc. can be mentioned.
  • the polycarboxylic acid include aliphatic polycarboxylic acids (oxalic acid, malonic acid, succinic acid, adipic acid, maleic acid, etc.), aromatic polycarboxylic acids (phthalic acid, etc.) and the like.
  • the central atom is bonded to at least two oxygen atoms, one oxygen atom is bonded to a carbonyl group, and the other oxygen atom is a carbon having no oxo group. It is bonded to an atom.
  • the plurality of coordination atoms contained in the coordination compound may contain an oxygen atom bonded to a carbonyl group and a nitrogen atom.
  • the number of oxygen atoms and nitrogen atoms may be one or plural.
  • at least one of the plurality of oxygen atoms may be bonded to a carbonyl group.
  • it may further contain an oxygen atom bonded to a carbon atom having no oxo group.
  • the organic molecule containing the oxygen atom and the nitrogen atom as a coordination atom include an aminocarboxylic acid-based chelating agent.
  • Aminocarboxylic acid-based chelating agents include ethylenediamine tetraacetic acid, nitrilotriacetic acid, diethylenetriaminepentacetic acid, hydroxyethylethylenediaminetriacetic acid, hydroxyethyliminodiacetic acid, L-aspartic acid-N, N-diacetic acid, and hydroxyiminodiacetic acid. And so on.
  • the central atom is boron or aluminum, for example, a tetracoordinated complex anion can be formed.
  • a complex anion in which two organic molecules (eg, hydroxy acid and dicarboxylic acid) are coordinated with a boron atom or an aluminum atom.
  • the central atom is silicon, for example, a pentacoordinated or hexacoordinated complex anion can be formed.
  • the coordination compound preferably contains at least one selected from the group consisting of borodisalicylic acid, borodiglycolic acid and borodiglycic acid.
  • the acid component may contain an oxo acid other than the first acid component as the second acid component.
  • the oxo acid of the secondary acid component does not contain an organic carboxylic acid.
  • an organic carboxylic acid organic molecule having a carboxy group
  • an oxo acid other than the organic carboxylic acid are produced by hydrolysis of the coordination compound, the equilibrium reaction is carried out by including the secondary acid component together with the coordination compound in the liquid component.
  • the hydrolysis reaction of the coordinating compound is suppressed, and the production of organic carboxylic acids that corrode the anode is suppressed.
  • the secondary acid component is preferably the same as the oxo acid other than the organic carboxylic acid produced by the hydrolysis of the coordination compound.
  • the second acid component may be an inorganic acid.
  • the inorganic acid include boric acid, phosphoric acid, phosphorous acid, hypophosphoric acid, sulfuric acid and the like.
  • boric acid is preferable as the secondary acid component. Hydrolysis of the coordination compound formed by an organic carboxylic acid such as salicylic acid and boric acid is easily suppressed, and corrosion of the anode body by the degrading acid is easily suppressed.
  • the above-mentioned coordination compound having excellent thermal stability exists without being decomposed, and deterioration of the acid component due to heat is easily suppressed.
  • the oxo acid / organic molecule is preferably 0.05 or more and 30 or less, and more preferably 0.5 or more and 30 or less. be. In this case, the pH of the liquid component is maintained at an appropriate level, and the hydrolysis of the coordination compound is easily suppressed efficiently.
  • an amine compound As the base component, an amine compound can be used. Amine compounds are advantageous for maintaining low ESR during long-term use of electrolytic capacitors.
  • an aliphatic amine, an aromatic amine, a heterocyclic amine or the like can be used. Of these, aliphatic amines having a molecular weight of 72 or more and 102 or less are preferable because they have a high degree of dissociation.
  • the amine compound may contain at least one selected from the group consisting of a primary amine compound, a secondary amine compound and a tertiary amine compound.
  • a primary amine compound a secondary amine compound
  • a tertiary amine compound a tertiary amine compound.
  • the thermal stability of the liquid component is enhanced, and the heat resistance of the electrolytic capacitor is improved.
  • the primary to tertiary amine compounds include methylamine, dimethylamine, monoethyldimethylamine, trimethylamine, ethylamine, diethylamine, triethylamine, ethylenediamine, N, N-diisopropylethylamine, tetramethylethylenediamine, hexamethylenediamine, spermidine, and the like.
  • Examples thereof include spermin, amantadin, aniline, phenethylamine, toluidine, pyrrolidine, piperidine, piperazine, morpholine, imidazole, imidazoline, pyridine, pyridazine, pyrimidine, pyrazine and 4-dimethylaminopyridine.
  • the amine compound one kind may be used alone, or two or more kinds may be used in combination. Of these, tertiary amines such as triethylamine and monoethyldimethylamine are preferable.
  • the liquid component preferably contains more acid components than the base component.
  • the acid component lowers the pH of the electrolytic solution from the initial stage and suppresses dedoping of the dopant from the conductive polymer.
  • By containing a larger amount of the acid component than the base component it is possible to suppress dedoping of the dopant from the conductive polymer (deterioration of the solid electrolyte).
  • the acid component since the acid component contributes to the repair function of the dielectric layer of the liquid component, it is preferable that the acid component contains a larger amount of the acid component than the basic component.
  • the molar ratio of the acid component to the base component is, for example, 1 or more, and may be 1.1 or more. It is preferably 1.5 or more, more preferably 1.5 or more and 10.0 or less.
  • the pH of the liquid component may be 4.0 or less, 0.1 or more, and 3.5 or less.
  • the total content of the acid component and the base component in the liquid component may be, for example, 3% by mass or more and 30% by mass or less, and 5% by mass or more and 25% by mass or less with respect to the entire liquid component. There may be. In the above range, the repairability of the dielectric layer is improved, and a liquid component having good conductivity can be easily obtained.
  • Solvents include at least water and polyol compounds.
  • the water contained in the liquid component may be derived from the water contained in the dispersion liquid of the conductive polymer compound used in the process of covering the surface of the dielectric layer with the film of the conductive polymer compound. Further, it may be derived from water contained in each member such as a separator or a metal foil, or a polyol compound.
  • the content of water with respect to the whole of the liquid component may be 0.1% by mass or more and 30% by mass or less, 0.1% by mass or more and 15% by mass or less, and may be 0.1% by mass.
  • the above may be 10% by mass or less.
  • the content of water with respect to the whole of the liquid component may be 1% by mass or more and 15% by mass, or may be 1% by mass or more and 10% by mass or less.
  • the repair function of the dielectric layer of the liquid component is likely to be exhibited.
  • the repairability of the dielectric layer of the liquid component is further improved.
  • the liquid component contains an antioxidant, so that the oxidative deterioration of the conductive polymer compound is easily suppressed, and the increase in ESR due to the deterioration of the conductive polymer compound is easily suppressed. ..
  • the water content is 10% by mass or less, the oxidative deterioration of the conductive polymer compound is further suppressed.
  • the content of water with respect to the whole liquid component may be 0.1% by mass or more and 5% by mass or less, 0.5% by mass or more and 5% by mass or less, and 1% by mass or more and 5%. It may be mass% or less.
  • the water content is 5% by mass or less, the increase in the internal pressure of the electrolytic capacitor during the reflow process and the accompanying deformation of the sealing portion are likely to be suppressed.
  • the content of water with respect to the whole liquid component may be 5% by mass or more and 10% by mass or less.
  • the content of the above water is 5% by mass or more, a large amount of decomposing acid is generated by hydrolysis of the coordination compound, but by using an antioxidant and a polyol compound, the effect of suppressing corrosion of the anode by the decomposing acid is achieved. Is remarkably obtained.
  • the water content in the liquid component is determined by disassembling the electrolytic capacitor, taking out a sample of the liquid component, and measuring the water content in the sample using a Karl Fischer titer.
  • the polyol compound easily dissolves the coordination compound and easily esterifies the decomposing acid of the coordination compound.
  • the ratio of the polyol compound to the solvent is, for example, 5% by mass or more, and may be 50% by mass or more. All solvents other than water may be polyol compounds.
  • the polyol compound one kind may be used alone, or two or more kinds may be used in combination.
  • Gas chromatography-mass spectrometry (GC / MS) or the like can be used for the analysis of the polyol compound.
  • the polyol compound preferably contains a glycerin compound.
  • the conductive polymer compound swells and the orientation of the conductive polymer compound is improved.
  • the conductivity of the conductive polymer compound is improved, and the ESR is likely to be reduced.
  • the glycerin compound has a high boiling point, and the permeation from the sealing portion of the electrolytic capacitor to the outside is suppressed. Therefore, the decrease of the solvent in the liquid component due to the exposure of the electrolytic capacitor to a high temperature is suppressed, the repairability of the dielectric layer is improved, and the withstand voltage is improved.
  • the degrading acid having a carboxy group is more easily esterified with the glycerin compound than the phenolic antioxidant having a hydroxy group bonded to the aromatic ring.
  • the solvent contains a glycerin compound, the effect of esterification of the degrading acid having a carboxy group on the phenolic antioxidant is reduced, and the function of CHO-forming the degrading acid in the phenolic antioxidant and the conductive polymer compound. The function of suppressing oxidative deterioration is likely to be efficiently exerted.
  • Glycerin compounds include glycerin, polyglycerin, and derivatives thereof.
  • the glycerin or polyglycerin derivative include an ester in which at least a part of the hydroxy group of glycerin or polyglycerin is esterified, an alkylene oxide adduct of glycerin or polyglycerin, and the like.
  • polyglycerin include diglycerin and triglycerin.
  • Polyglycerin contains a repeating structure of glycerin units.
  • the number of repetitions of the glycerin unit contained in polyglycerin is, for example, 2 or more and 15 or less, may be 2 or more and 12 or less, may be 2 or more and 10 or less, and may be 2 or more and 6 or less. May be good.
  • the weight average molecular weight of polyglycerin is, for example, preferably 200 or more and 1000 or less, and more preferably 300 or more and 800 or less.
  • the polyol compound preferably contains a glycol compound.
  • a glycol compound for example, an alkylene glycol such as ethylene glycol
  • the conductive polymer compound swells and the orientation of the conductive polymer compound is improved.
  • the conductivity of the conductive polymer compound is improved, and the ESR is likely to be reduced.
  • the glycol compound is hard to evaporate, the decrease of the solvent in the liquid component due to the exposure of the electrolytic capacitor to a high temperature is suppressed, the repairability of the dielectric layer is improved, and the withstand voltage is improved.
  • Glycol compounds include alkylene glycols, polyalkylene glycols and the like.
  • the polyalkylene glycol may be a homopolymer or a copolymer (for example, a copolymer containing ethylene oxide (EO) unit and propylene oxide (PO) unit, etc.).
  • the weight average molecular weight of the polyalkylene glycol is, for example, 100 or more and 3000 or less, and may be 100 or more and 2000 or less.
  • the weight average molecular weight of polyethylene glycol is, for example, 100 or more and 600 or less, and may be 100 or more and 400 or less.
  • glycol compound examples include ethylene glycol, propylene glycol, butylene glycol, hexylene glycol, diethylene glycol, triethylene glycol and the like, and among them, ethylene glycol is preferable.
  • Ethylene glycol has a low viscosity among glycol compounds and easily dissolves acid components and base components including coordination compounds. Further, ethylene glycol has high thermal conductivity and excellent heat dissipation, which is advantageous for improving the heat resistance of the electrolytic capacitor.
  • the solvent may contain components other than the polyol compound and water.
  • a component include a sulfone compound, a sulfoxide compound, a lactone compound, a carbonate compound and the like.
  • Examples of the sulfone compound include dimethyl sulfone, diethyl sulfone, sulfolane, 3-methyl sulfolane and the like.
  • Examples of the sulfoxide compound include dimethyl sulfoxide and diethyl sulfoxide.
  • Examples of the lactone compound include ⁇ -butyrolactone and ⁇ -valerolactone.
  • Examples of the carbonate compound include dimethyl carbonate, diethyl carbonate, ethylmethyl carbonate, ethylene carbonate, propylene carbonate, fluoroethylene carbonate and the like.
  • the components other than the polyol compound one kind may be used alone, or two or more kinds may be used in combination.
  • ⁇ -butyrolactone and sulfolane are preferable as the components other than the organic compound having a hydroxy group.
  • the antioxidant may contain at least one selected from the group consisting of phenol-based antioxidants, amine-based antioxidants, phosphorus-based antioxidants, sulfur-based antioxidants and aliphatic antioxidants. Among them, a phenolic antioxidant is preferable from the viewpoint of reactivity with oxygen.
  • the phenolic antioxidant preferably contains at least one selected from the group consisting of monophenolic antioxidants, bisphenolic antioxidants and polyphenolic antioxidants. Of these, polyphenols are preferable from the viewpoint of having many functional groups having good reactivity with oxygen.
  • the monophenolic antioxidant preferably contains 2,6-di-tert-butyl-4-methylphenol, butylhydroxyanisole, sesamol, tocopherol, tocotrienol, p-nitrophenol and the like. Further, the monophenolic antioxidant may contain mono, di, or tri ( ⁇ -methylbenzyl) phenol, trolox, normelatonin, ferulic acid and the like.
  • the bisphenol-based antioxidant preferably contains anoxomer or the like.
  • the bisphenol antioxidants are 2,2'-methylenebis (4-ethyl-6-tert-butylphenol), 2,2'-methylenebis (4-methyl-6-tert-butylphenol), 4,4'-. Butyldenbis (3-ethyl-6-tert-butylphenol), 4,4'-thiobis (3-ethyl-6-tert-butylphenol), butylation reaction products of p-cresol and dicyclopentadiene and the like may be included.
  • the polyphenolic antioxidant is preferably 2,5-di-tert-butylhydroquinone, 2,5-di-tert-amylhydroquinone, gallic acid, propyl gallate, chlorogenic acid, catechin, epigalocatechin, epigallo.
  • catechin gallate rosmarinic acid, genquanin, luteolin, carnosic acid, carnosol, ursoleic acid, pyrogallol, kebrazinic acid, hydroxytyrosol, dopamine, caffeic acid, adrenaline, noradrenaline, catechol, bovine all, hydroquinone, resorcinol and the like.
  • the polyphenolic antioxidants include protocatechuic acid, rutin, gnetin C, theaflavin, luteolin, resveratrol, pinocembrin, pinobanksin, 1,3,5-tris (3,5-di-tert-butyl-4-hydroxy).
  • Benzyl) -1,3,5-triazine-2,4,6 (1H, 3H, 5H) -trione, 4,4', 4 "-(1-methylpropanol-3-iriden) tris (6-tert) -Butyl-m-cresol) and the like may be contained.
  • Amine-based antioxidants include aromatic secondary amine-based antioxidants, benzotriazole-based antioxidants, benzimidazole-based antioxidants, amine-ketone-based antioxidants, and the like.
  • the aromatic secondary amine-based antioxidant includes N-phenyl-1-naphthylamine, diphenylamine-based antioxidant, phenylenediamine-based antioxidant, and the like.
  • Diphenylamine-based antioxidants include alkylated diphenylamines such as p, p'-dioctyldiphenylamine, 4,4'-bis ( ⁇ , ⁇ -dimethylbenzyl) diphenylamines, p- (p-toluenesulfonylamide) diphenylamines and the like.
  • Phenylenediamine-based antioxidants include N, N'-di-2-naphthyl-p-phenylenediamine, N-phenyl-N'-isopyrropyr-p-phenylenediamine, N-phenyl-N'-(1,3-). It contains dimethylbutyl) -p-phenylenediamine, N-phenyl-N'-(3-methacryloyloxy-2-hydroxypropyl) -p-phenylenediamine and the like.
  • Benzotriazole-based antioxidants include benzotriazole and the like.
  • Benzimidazole-based antioxidants include benzimidazole, 2-mercaptobenzoimidazole, 2-mercaptomethylbenzoimidazole, imidazole dipeptide and the like.
  • Amine-ketone antioxidants are 2,2,4-trimethyl-1,2-dihydroquinoline polymer, 6-ethoxy-1,2-dihydro-2,2,4-trimethylquinoline, reaction of diphenylamine with acetone. Includes substances, acetylcysteine, melatonin, etc.
  • Phosphorus-based antioxidants include phosphoric acid ester-based antioxidants, phosphite ester-based antioxidants, and the like.
  • ester include monoalkyl esters, dialkyl esters, trialkyl esters and the like.
  • phosphite ester-based antioxidant include tris (nonylphenyl) phosphite and the like.
  • Sulfur-based antioxidants include thioether-based antioxidants, isothiocyanates, sulfites (salts), pyrosulfites (salts), and the like.
  • Thioether-based antioxidants include phenothiazine, dibenzyldisulfide, diacetylsulfide, dilauryl thiodipropionate and the like.
  • Aliphatic antioxidants include citric acid, L-ascorbic acid, erythorbic acid, ethylenediaminetetraacetic acid and the like.
  • the antioxidant one type may be used alone, or two or more types may be used in combination.
  • the content of the antioxidant in the liquid component is, for example, 0.5% by mass or more and 30% by mass or less with respect to the entire liquid component.
  • Liquid chromatography (LC), gas chromatography-mass spectrometry (GC / MS), or the like can be used for the analysis of the antioxidant.
  • the molar ratio of the antioxidant to the organic molecule in the coordination compound may be 0.05 or more and 30 or less, and 0.5 or more and 30 or less. May be good. In this case, it is easy to efficiently convert the degrading acid derived from the organic molecule into CHO by the antioxidant.
  • the capacitor element contains at least an anode having a dielectric layer on its surface and a conductive polymer compound covering at least a part of the dielectric layer.
  • the capacitor element will be described in detail.
  • the anode body can contain a valve acting metal, an alloy containing a valve acting metal, a compound containing a valve acting metal, and the like. These materials can be used alone or in combination of two or more.
  • the valve acting metal for example, aluminum, tantalum, niobium, and titanium are preferably used.
  • the anode body having a porous surface can be obtained by, for example, roughening the surface of a base material (foil-shaped or plate-shaped base material, etc.) containing a valve acting metal by etching or the like.
  • the anode body may be a molded body of particles containing a valve acting metal or a sintered body thereof.
  • the sintered body has a porous structure.
  • the dielectric layer is formed by anodizing the valve acting metal on the surface of the anode body by chemical conversion treatment or the like.
  • the dielectric layer may be formed so as to cover at least a part of the anode body.
  • the dielectric layer is usually formed on the surface of the anode. Since the dielectric layer is formed on the porous surface of the anode body, it is formed along the inner wall surface of the holes and pits on the surface of the anode body.
  • the dielectric layer contains an oxide of the valve acting metal.
  • the dielectric layer when tantalum is used as the valve acting metal contains Ta 2 O 5
  • the dielectric layer when aluminum is used as the valve acting metal contains Al 2 O 3 .
  • the dielectric layer is not limited to this, and may be any one that functions as a dielectric.
  • the dielectric layer is formed along the surface of the anode, including the inner wall of the hole.
  • Examples of the conductive polymer compound include ⁇ -conjugated polymer compounds.
  • Examples of the conductive polymer compound include polypyrrole, polythiophene, polyfuran, polyaniline, polyacetylene, polyphenylene, polyphenylene vinylene, polyacene, polythiophene vinylene and the like. These may be used alone or in combination of two or more kinds, or may be a copolymer of two or more kinds of monomers.
  • the weight average molecular weight of the conductive polymer compound is, for example, 1000 to 100,000.
  • polypyrrole, polythiophene, polyfuran, polyaniline and the like mean polymers having polypyrrole, polythiophene, polyfuran, polyaniline and the like as basic skeletons, respectively. Therefore, polypyrrole, polythiophene, polyfuran, polyaniline and the like may also contain their respective derivatives.
  • polythiophene includes poly (3,4-ethylenedioxythiophene) and the like.
  • the conductive polymer compound can be doped with a dopant.
  • the dopant may be a polyanion.
  • Specific examples of the polyanion include polyvinyl sulfonic acid, polystyrene sulfonic acid, polyallyl sulfonic acid, polyacrylic sulfonic acid, polymethacrylic sulfonic acid, poly (2-acrylamide-2-methylpropanesulfonic acid), polyisoprene sulfonic acid, and poly. Acrylic acid and the like can be mentioned. These may be used alone or in combination of two or more. Further, these may be polymers of a single monomer or may be a copolymer of two or more kinds of monomers. Of these, a polyanion derived from polystyrene sulfonic acid is preferable.
  • a conductive polymer layer (solid electrolyte layer).
  • the conductive polymer layer may contain a dopant together with the conductive polymer compound.
  • the conductive polymer layer constitutes a part of the cathode portion together with the cathode body.
  • the conductive polymer layer may further contain an additive, if necessary.
  • the conductive polymer layer can be formed, for example, by chemically polymerizing and / or electrolytically polymerizing the raw material monomer on the dielectric layer. Alternatively, it can be formed by contacting the dielectric layer with a solution in which the conductive polymer compound is dissolved or a dispersion in which the conductive polymer compound is dispersed. The conductive polymer layer may be formed so as to cover at least a part of the dielectric layer.
  • Cathode By including the polyol compound and the antioxidant in the liquid component containing the coordination compound and water, the CHO conversion and esterification of the degrading acid generated by the hydrolysis of the coordination compound progresses, and the corrosion of the cathode body due to the decomposing acid is suppressed. Will be done.
  • the corrosion of the cathode body progresses and impurities are formed on the surface of the cathode body, the interfacial resistance between the cathode body and the conductive polymer compound increases, and the ESR increases.
  • a metal foil may be used for the cathode body.
  • the type of metal is not particularly limited, but it is preferable to use a valve acting metal such as aluminum, tantalum, niobium, or an alloy containing a valve acting metal. If necessary, the surface of the metal foil may be roughened.
  • the surface of the metal foil may be provided with a chemical conversion film, or may be provided with a metal (dissimilar metal) or non-metal film different from the metal constituting the metal foil. Examples of the dissimilar metal and the non-metal include a metal such as titanium and a non-metal such as carbon.
  • a separator When the metal foil is used for the cathode body, a separator may be arranged between the metal foil and the anode body.
  • the separator is not particularly limited, and for example, a non-woven fabric containing fibers of cellulose, polyethylene terephthalate, vinylon, polyamide (for example, aromatic polyamide such as aliphatic polyamide and aramid) may be used.
  • the electrolytic capacitor may have at least one capacitor element, and may have a plurality of capacitor elements.
  • the number of capacitor elements included in the electrolytic capacitor may be determined according to the application.
  • FIG. 1 is a schematic cross-sectional view of an electrolytic capacitor according to the present embodiment
  • FIG. 2 is a schematic view showing a part of a capacitor element related to the electrolytic capacitor.
  • the electrolytic capacitor shown in FIG. 1 includes a capacitor element 10, a liquid component (not shown), a bottomed case 11 that houses the capacitor element 10 and the liquid component, and a sealing member 12 that closes the opening of the bottomed case 11.
  • the seat plate 13 that covers the sealing member 12, the lead wires 14A and 14B that are derived from the sealing member 12 and penetrate the seat plate 13, and the lead tabs 15A and 15B that connect the lead wires and the electrodes of the capacitor element 10. , Equipped with.
  • the open end of the bottomed case 11 is curled so as to be crimped to the sealing member 12.
  • the capacitor element 10 is manufactured from a winding body as shown in FIG.
  • the wound body is a semi-finished product of the capacitor element 10, and means that the conductive polymer compound is not arranged between the anode body 21 having a dielectric layer on the surface and the cathode body 22.
  • the winding body is formed by winding an anode body 21 connected to the lead tab 15A and a cathode body 22 connected to the lead tab 15B via a separator 23.
  • the outermost circumference of the winding body is fixed by the winding stop tape 24. Note that FIG. 2 shows a partially unfolded state before fixing the outermost circumference of the winding body.
  • the anode body 21 is provided with a metal foil whose surface is roughened, and a dielectric layer is formed on the roughened surface.
  • the capacitor element 10 is formed by adhering a conductive polymer compound to at least a part of the surface of the dielectric layer.
  • Step of preparing the anode body 21 and the cathode body 22 having a dielectric layer As a raw material for the anode body 21 and the cathode body 22, a metal foil containing a valve acting metal is used. In the case of the anode body 21, the surface of the metal foil is roughened by etching or the like, and a plurality of irregularities are formed on the surface of the metal foil. Next, a dielectric layer is formed on the surface of the roughened metal foil by chemical conversion treatment or the like. If necessary, the surface of the cathode body 22 may be roughened.
  • the anode body 21 and the cathode body 22 are wound around the separator 23 to form a wound body.
  • the lead tabs 15A and 15B may be wound while being wound, and the lead tabs 15A and 15B may be planted from the winding body as shown in FIG.
  • the winding stop tape 24 is arranged on the outer surface of the cathode body 22 located on the outermost layer of the winding body, and the end portion of the cathode body 22 is fixed.
  • the wound body may be further subjected to chemical conversion treatment in order to form a dielectric layer on the cut surface of the anode body 21.
  • the dielectric layer is impregnated with a dispersion liquid of the conductive polymer compound to form a film of the conductive polymer compound covering at least a part of the dielectric layer.
  • the capacitor element 10 in which the conductive polymer compound is arranged between the anode body 21 and the cathode body 22 is obtained.
  • the step of applying the dispersion liquid of the conductive polymer compound to the surface of the dielectric layer may be repeated twice or more.
  • the capacitor element 10 may be impregnated with a liquid component.
  • an electrolytic capacitor containing a conductive polymer compound and a liquid component can be obtained.
  • an electrolytic capacitor having an excellent repair function of the dielectric layer can be obtained.
  • the material of the bottomed case 11 for storing the capacitor element 10 together with the liquid component in the bottomed case 11 so that the lead wires 14A and 14B are located on the opening side of the bottomed case 11 is aluminum, stainless steel, copper, iron, etc. Examples include metals such as brass and alloys containing these.
  • the opening of the bottomed case 11 is closed by the sealing member 12 through which the lead wires 14A and 14B penetrate, the opening end is crimped to the sealing member 12 and curled, and the seat plate 13 is arranged in the curled portion.
  • the aging process may be performed while applying the rated voltage.
  • the winding type electrolytic capacitor has been described, but the scope of application of the present invention is not limited to the above, and other electrolytic capacitors, for example, chip type electrolysis using a metal sintered body as an anode body. It can also be applied to capacitors and laminated electrolytic capacitors that use a metal plate as an anode.
  • An aluminum foil having a thickness of 100 ⁇ m was subjected to an etching treatment to roughen the surface of the aluminum foil. Then, a dielectric layer was formed on the surface of the aluminum foil by chemical conversion treatment. The chemical conversion treatment was carried out by immersing an aluminum foil in an ammonium adipate solution and applying a voltage of 45 V to the aluminum foil. Then, the aluminum foil was cut to prepare an anode body.
  • the anode lead tab and the cathode lead tab were connected to the anode body and the cathode body, and the anode body and the cathode body were wound through the separator while winding the lead tab.
  • the end portion of the outer surface of the winding body was fixed with a winding stop tape to prepare a winding body.
  • An anode lead wire and a cathode lead wire were connected to the end of each lead tab protruding from the winding body.
  • the produced wound body was subjected to chemical conversion treatment again to form a dielectric layer at the cut end of the anode body.
  • the winding body was immersed in the polymer dispersion contained in a predetermined container for 5 minutes in a reduced pressure atmosphere (40 kPa), and then the winding body was pulled up from the polymer dispersion. Next, the wound body impregnated with the polymer dispersion was dried in a drying oven at 150 ° C. for 20 minutes to form a conductive polymer layer covering at least a part of the dielectric layer. The capacitor element was formed in this way.
  • liquid component 12% by mass of a salt formed by the above acid component and base component was added.
  • the molar ratio of the first acid component / base component was 1.0.
  • Pyrogallol was used as the antioxidant.
  • the content of the antioxidant in the liquid component was set to 6% by mass with respect to the entire liquid component.
  • Comparative Examples 1 to 3, 6, 9 and 11 the liquid component did not contain an antioxidant.
  • ESR initial ESR (Z0)
  • Z0 initial ESR
  • the water content was as large as 5% by mass or more and 10% by mass or less, and a large amount of decomposing acid was generated, but the ESR and leakage current after storage were sufficiently reduced.
  • the antioxidant and the polyol compound in the liquid component by including the antioxidant and the polyol compound in the liquid component, the effect of suppressing the corrosion of the anode and the cathode by the decomposing acid was remarkably obtained.
  • the electrolytic capacitor of Example 14 using GLY had a smaller ESR and leakage current after storage than the electrolytic capacitor of Example 3 using EG.
  • the electrolytic capacitor according to the present invention is suitably used for applications where high ESR and leakage current are small and high reliability is required.

Landscapes

  • Engineering & Computer Science (AREA)
  • Power Engineering (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
PCT/JP2021/035092 2020-09-25 2021-09-24 電解コンデンサ Ceased WO2022065434A1 (ja)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US18/246,089 US12300445B2 (en) 2020-09-25 2021-09-24 Electrolytic capacitor
CN202180064741.4A CN116235266A (zh) 2020-09-25 2021-09-24 电解电容器
JP2022552071A JPWO2022065434A1 (https=) 2020-09-25 2021-09-24

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2020161360 2020-09-25
JP2020-161360 2020-09-25

Publications (1)

Publication Number Publication Date
WO2022065434A1 true WO2022065434A1 (ja) 2022-03-31

Family

ID=80846638

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2021/035092 Ceased WO2022065434A1 (ja) 2020-09-25 2021-09-24 電解コンデンサ

Country Status (4)

Country Link
US (1) US12300445B2 (https=)
JP (1) JPWO2022065434A1 (https=)
CN (1) CN116235266A (https=)
WO (1) WO2022065434A1 (https=)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE112021002147T5 (de) 2020-04-03 2023-03-02 Vladimir Borisovich Chernyshev Verfahren und anlage zur behandlung einer akuten lungeninsuffizienz
WO2024010063A1 (ja) * 2022-07-06 2024-01-11 パナソニックＩｐマネジメント株式会社 電解コンデンサ
WO2024181213A1 (ja) * 2023-02-28 2024-09-06 パナソニックＩｐマネジメント株式会社 電解コンデンサおよびその製造方法
WO2024181509A1 (ja) * 2023-03-02 2024-09-06 日本ケミコン株式会社 固体電解コンデンサ及び製造方法
US20250046528A1 (en) * 2021-12-27 2025-02-06 Panasonic Intellectual Property Management Co., Ltd. Electrolytic capacitor and liquid component for electrolytic capacitor
WO2025047356A1 (ja) * 2023-08-31 2025-03-06 パナソニックＩｐマネジメント株式会社 電解コンデンサおよび電解コンデンサ用液状成分

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004186580A (ja) * 2002-12-05 2004-07-02 Nippon Chemicon Corp 電解コンデンサ
WO2016174807A1 (ja) * 2015-04-28 2016-11-03 パナソニックＩｐマネジメント株式会社 電解コンデンサ
WO2017073062A1 (ja) * 2015-10-30 2017-05-04 パナソニックＩｐマネジメント株式会社 電解コンデンサおよびその製造方法
WO2020022471A1 (ja) * 2018-07-26 2020-01-30 パナソニックＩｐマネジメント株式会社 電解コンデンサ
JP2020107791A (ja) * 2018-12-28 2020-07-09 パナソニックＩｐマネジメント株式会社 電解コンデンサ

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5052746B2 (ja) 2004-10-12 2012-10-17 パナソニック株式会社 電解コンデンサ
JP2007246840A (ja) * 2006-03-17 2007-09-27 Fujifilm Corp インクジェット記録用インク組成物、平版印刷版の製造方法および平版印刷版
US10749153B2 (en) * 2016-01-08 2020-08-18 Zeon Corporation Sealant for electrochemical device in which non-aqueous electrolysis solution is used and sealant composition for electrochemical device
US20170372842A1 (en) * 2016-06-27 2017-12-28 Capacitor Sciences Incorporated Electro-polarizable complex compound and capacitor
WO2019146564A1 (ja) * 2018-01-23 2019-08-01 Tdk株式会社 ガス検知シート及びガス検知シートを備えた電気化学素子

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004186580A (ja) * 2002-12-05 2004-07-02 Nippon Chemicon Corp 電解コンデンサ
WO2016174807A1 (ja) * 2015-04-28 2016-11-03 パナソニックＩｐマネジメント株式会社 電解コンデンサ
WO2017073062A1 (ja) * 2015-10-30 2017-05-04 パナソニックＩｐマネジメント株式会社 電解コンデンサおよびその製造方法
WO2020022471A1 (ja) * 2018-07-26 2020-01-30 パナソニックＩｐマネジメント株式会社 電解コンデンサ
JP2020107791A (ja) * 2018-12-28 2020-07-09 パナソニックＩｐマネジメント株式会社 電解コンデンサ

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE112021002147T5 (de) 2020-04-03 2023-03-02 Vladimir Borisovich Chernyshev Verfahren und anlage zur behandlung einer akuten lungeninsuffizienz
US20250046528A1 (en) * 2021-12-27 2025-02-06 Panasonic Intellectual Property Management Co., Ltd. Electrolytic capacitor and liquid component for electrolytic capacitor
WO2024010063A1 (ja) * 2022-07-06 2024-01-11 パナソニックＩｐマネジメント株式会社 電解コンデンサ
WO2024181213A1 (ja) * 2023-02-28 2024-09-06 パナソニックＩｐマネジメント株式会社 電解コンデンサおよびその製造方法
WO2024181509A1 (ja) * 2023-03-02 2024-09-06 日本ケミコン株式会社 固体電解コンデンサ及び製造方法
WO2025047356A1 (ja) * 2023-08-31 2025-03-06 パナソニックＩｐマネジメント株式会社 電解コンデンサおよび電解コンデンサ用液状成分

Also Published As

Publication number Publication date
JPWO2022065434A1 (https=) 2022-03-31
CN116235266A (zh) 2023-06-06
US20230368982A1 (en) 2023-11-16
US12300445B2 (en) 2025-05-13

Similar Documents

Publication Publication Date Title
WO2022065434A1 (ja) 電解コンデンサ
CN108022756B (zh) 电解电容器
JP7289071B2 (ja) 電解コンデンサ
US10354806B2 (en) Electrolytic capacitor and method for manufacturing same
TWI875935B (zh) 固體電解電容器
US10755863B2 (en) Electrolytic capacitor
JP6610264B2 (ja) 固体電解コンデンサ及びその製造方法
JP2011109023A (ja) 固体電解コンデンサおよびその製造方法
US20260112544A1 (en) Electrolytic capacitor
JPWO2019088059A1 (ja) 電解コンデンサ
JPWO2020022472A1 (ja) 電解コンデンサ
JP6767527B2 (ja) ハイブリッド型電解コンデンサ用電解液
WO2022044636A1 (ja) 電解コンデンサ
CN114830274A (zh) 电解电容器用液状成分及电解电容器
JP2004253537A (ja) 固体電解コンデンサ
EP3270390B1 (en) Electrolytic solution for aluminum electrolytic capacitor and aluminum electrolytic capacitor using same
US12437935B2 (en) Solid electrolytic capacitor containing oxygen-containing amine without hydroxy group and method for manufacturing same
US20240177942A1 (en) Liquid component for electrolytic capacitor and electrolytic capacitor
WO2026004777A1 (ja) 電解コンデンサ
WO2025070507A1 (ja) 電解コンデンサ
CN120826754A (zh) 固体电解电容器、平滑电路、滤波电路和制造方法
TW202603760A (zh) 電解液、電解電容器及電解電容器之製造方法
CN118116743A (zh) 电解电容器和电解电容器用液态成分
CN121713264A (zh) 电解电容器和电解电容器用液态成分
HK40103661A (zh) 电解电容器

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: 21872563

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2022552071

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 21872563

Country of ref document: EP

Kind code of ref document: A1

WWG Wipo information: grant in national office

Ref document number: 18246089

Country of ref document: US