JP2010194759A - Resin-coated stainless steel foil for electricity accumulation device container - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide resin-coated stainless steel foil which, in spite of the use of the stainless steel foil making thickness reduction for increasing an electric capacity and a strength improvement for improving safety compatible, in a temperature cycle test indispensable for an electricity accumulation device, maintains firm adhesive force in a surface outside a container on the entire surface of a laminate, does not peel, prevents the mixing of dirt with foreign substances, and is excellent in cleanness and designability. <P>SOLUTION: In the resin-coated stainless steel foil for the electricity accumulation device container, the resin-coated stainless steel foil is obtained by laminating a resin on both sides of the stainless steel foil 1, and when processed into the electricity accumulation device container, on the surface of the stainless steel foil to be the outside of the container, through an adhesive (B) layer 3 developing adhesive force by heating, a resin composition (A) layer 2 containing at least 50 mass% in total of at least one or at least two resins 5 selected from among a polyolefin, a polyester, a polyamide, and a polyimide is laminated by heat lamination. In addition, numeral 4 represents a surface treatment layer, for example, of a chromate. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

  The present invention relates to a resin-coated stainless steel foil for a power storage device container that has excellent high-temperature cycle resistance, cleanliness, and design properties, and few product defects.

  Power storage including secondary batteries and capacitors such as nickel-cadmium, nickel-hydrogen, and lithium-ion batteries for electronic devices and electronic parts, especially mobile phones, laptop computers, video cameras, satellite communications, electric / hybrid vehicles, etc. The device is widely used. Conventionally, a secondary battery using a strong alkaline electrolyte such as nickel-cadmium, nickel-hydrogen, etc. has used a case made of a nickel-plated cold-rolled steel plate or a plastic case. Further, even in a battery using a non-aqueous electrolyte such as a lithium ion battery, an electrolyte incorporated in an aluminum pouch is wrapped in a plastic case, or a nickel-plated steel plate or a stainless steel plate case is used.

  In recent years, with the miniaturization of electronic and electrical components, there has been a demand for miniaturization and weight reduction of power storage devices such as secondary batteries and capacitors. Among these trends, the thinning of containers is attracting attention as a tool that can mount a large amount of electrolyte and ions in a limited volume and increase the electric capacity. However, if the strength of the container is reduced due to thinning, there is a risk that the content electrolyte solution may leak due to deformation or destruction when an external force or piercing is applied. There is a high possibility that the leakage of the electrolytic solution will cause a serious obstacle to the device in which the electricity storage device is built. Therefore, when the member of the container is plastic or aluminum, the strength is insufficient when the thickness is 200 μm or less, and a material with high strength is required for further thinning. In consideration of mass production, a general-purpose material is preferable.

  Stainless steel foil is a material that satisfies these required characteristics. Stainless steel foil is a thin foil made of stainless steel with a thickness of 200 μm or less, and the tensile strength and Vickers hardness of stainless steel are generally 2 to 10 times higher than that of plastic and aluminum. It is promising as a thin material for containers. It can be said that stainless steel foil is indispensable in the future development of electricity storage devices in order to achieve both a reduction in wall thickness for increasing electric capacity and an improvement in strength for improving safety.

  A typical example of an electricity storage device that has been reduced in size and weight in the prior art is a lithium ion secondary battery, and metal foils for the container are disclosed in Patent Documents 1 to 4 and the like. As shown in these techniques, a container of an electricity storage device using a metal foil is generally coated with a resin on both surfaces of the metal foil. Resin that coats the outer surface of the container gives protection of the exterior such as insulation and corrosion resistance, design as a label, workability, etc., and heat sealability for packing with the resin on the inner surface side to mold the container Has been granted.

  In recent electronic products, particularly power storage devices using lithium ions, there have been many reports of fires, abnormal heat generation, and rupture accidents that are thought to be caused by some kind of product failure including contamination of dust and foreign substances. In addition to causing abnormalities in the contents and containers, it also causes a defective appearance of the product, so it is possible to achieve excellent cleanliness by eliminating dust and foreign substances, and eliminate defects in the adhesion between the resin and metal foil. It is important not to give out.

Japanese Patent Laid-Open No. 10-208708 JP 2001-30407 A Japanese Patent Laid-Open No. 2001-266809 JP 2000-123800 A

  However, in metal foils for power storage device containers that are coated with resin on both sides, as shown in Patent Documents 1 to 4, at least one side of the container, particularly the outer surface of the container is a method called dry lamination or wet lamination The resin is coated with. These methods require application of adhesive to the metal foil as the base material, resin film bonding, heat curing, solvent drying, curing, etc., and many materials and processes are complicated, so dust and foreign substances are mixed in. There are problems that are easy to do. Furthermore, in these methods, there is a strong concern that a poorly bonded portion will occur due to missing adhesive, and the adhesive force itself is generally lower than that of a thermal laminate, which may lead to product defects.

  On the other hand, in the thermal lamination which coats resin by thermocompression bonding, the number of processes is small and the laminating apparatus is simple. Therefore, it is easy to prevent dust and foreign matters from being mixed into the apparatus and materials, and easy to achieve excellent cleanliness. It is effective to coat the resin with a heat laminate because it can be adhered uniformly and satisfactorily without adhesion defects.

  However, when the resin is directly coated on the metal foil by thermal lamination, the following problems occur. Temperature standards are often imposed on the safety standards for power storage devices, and are exemplified in the `` Freedom CAR Electrical Energy Storage System Abuse Test Manual for Electric and Hybrid Electric Vehicle Applications '' by the US Department of Energy. Specified temperature cycle test at -40 ℃ and 80 ℃. When a metal cycle coated with resin by thermal lamination is subjected to a temperature cycle test that includes a temperature near or above the glass transition point of the resin, the thermal expansion and contraction of the resin is much greater than that of the metal foil. Therefore, a stress that the resin is pulled or compressed by the metal foil is generated, and a stress strain such as a warp that induces the separation of the resin is generated. And since most of resin used for the thermal lamination to metal foil has a glass transition point in these temperature ranges, or its vicinity, resin often peels.

  Further, since the stainless steel foil is harder than the aluminum foil and has a small thermal expansion and contraction, this tendency becomes more remarkable. The Young's modulus and rigidity of aluminum foil are about 1/4 to 1/3 of that of stainless steel foil, and the linear expansion coefficient is about 30 to 100% larger, reducing the thermal expansion and contraction of the resin. It is easy to be done. For this reason, the stress strain generated when the temperature cycle test is imposed is much larger and more severe in the stainless steel foil than in the case of the aluminum foil, so that the covering resin is very easily peeled off.

  In particular, in the storage device container application, the inner surface of the container is coated with polyethylene or polypropylene for the purpose of forming the container by heat sealing, and these thermal expansion and contraction are larger than that of the stainless steel foil. When the test is imposed, stress strain such as warpage that induces peeling becomes larger and worse for the resin coated on the outer surface side of the container than in the case of the stainless steel foil alone. Thus, the conventional thermal laminate has a problem with respect to temperature cycle resistance, which is peculiar to the case of using stainless steel foil for power storage device applications.

  In addition, when the resin is coated with a thermal laminate, since the resin is heated to a high temperature until the resin melts, the temperature difference between heating and actual use becomes large, and the heat shrinkage difference between the resin and the metal foil of the base material is large. Essentially easy to cause peeling. In particular, when the resin is crystalline, volume shrinkage due to crystallization is added, which may be further deteriorated. In addition, the resin is often formed into a film and coated, but once melted, the stretch ratio and crystallinity controlled in consideration of properties such as processability are greatly changed, which is not preferable.

  Therefore, the present invention provides a resin-coated stainless steel foil with excellent temperature cycle resistance that can solve the above-described problems and can be applied to a power storage device container with a resin-coated material by thermal lamination using a stainless steel foil as a base material. For the purpose.

As a result of imposing a temperature cycle test on the stainless steel foil coated with the resin composition with a thermal laminate and analyzing the peeling state of the resin composition in detail, the present inventors developed an adhesive force by heating. In the case where the adhesive is applied, the adhesive layer plays a role in buffering the stress strain caused by the difference in thermal expansion and contraction between the resin composition and the stainless steel foil. The present invention has been found based on this finding. In the stainless steel foil of the present invention, for use as an electricity storage device container, the opposite surface of the stainless steel foil coated with the resin composition (A) coated with the adhesive (B) is appropriately chromated or the like. Surface treatment is performed and a resin such as polyethylene or polypropylene is coated (FIG. 1). On the other hand, in the aluminum foil described in Patent Documents 1 to 4 as a metal foil for an electricity storage device container having a resin coated on both sides, the purpose of the resin coated on the outer surface of the container is to break a fragile aluminum foil. The main role is to improve workability, such as to prevent reinforcement. The strength and strength of the metal foil itself is completely different from that of stainless steel foil, which does not require a reinforcing material, and the required characteristics and purpose are completely different. In the prior art, in the manufacture of power storage device containers using stainless steel foil, the container Problems occur such as peeling of the resin coated on the outer surface and mixing of foreign substances such as dust. The present invention solves these problems, and in a stainless steel foil for an electricity storage device container, a normal product can be manufactured and provided stably and without difficulty even with an existing apparatus. That is, the gist of the present invention is as follows.
(1) A resin-coated stainless steel foil obtained by laminating a resin on both surfaces of a stainless steel foil, and when processed into an electricity storage device container, the adhesive force is applied by heating to the surface of the stainless steel foil on the outside of the container. Thermally laminating a resin composition (A) layer containing a total of 50 mass% or more of one or more resins selected from polyolefin, polyester, polyamide, and polyimide through an adhesive (B) layer that expresses A resin-coated stainless steel foil for an electricity storage device container, characterized in that it is laminated.
(2) the resin composition (A) layer having a thickness (t _a) and the adhesive ratio of (B) layer having a thickness _{(t b) (t b /} t a), is 0.01 to 0.5 (1) A resin-coated stainless steel foil for an electricity storage device container according to 1.
(3) The resin composition (A) layer tensile modulus (E _a) and the ratio of the adhesive tensile modulus (B) layer _{(E b) (E a /} E b), E a / E b The resin-coated stainless steel foil for an electricity storage device container according to (1) or (2), wherein> 1.
(4) The resin-coated stainless steel foil for an electricity storage device container according to any one of (1) to (3), wherein the resin composition (A) is a resin containing 50% by mass or more of polyester.
(5) The adhesive (B) is one or more selected from urethane-based resins, epoxy-based resins, nylon-based resins, unsaturated polyester-based resins, and any one of (1) to (4) The resin-coated stainless steel foil for an electricity storage device container as described.
(6) The resin-coated stainless steel foil for an electrical storage device container according to any one of (1) to (5), wherein the thickness (t _a ) of the resin composition (A) layer is 5 μm or more and 200 μm or less.
(7) The resin-coated stainless steel foil for an electricity storage device container according to any one of claims (1) to (6), further comprising a coating layer on the resin composition (A) layer.
(8) The resin laminated on the surface of the stainless steel foil that is the inside of the electricity storage device container is a resin composition (C) containing 50% by mass or more of polyolefin, and the thickness thereof is 10 μm or more and 150 μm or less (1) to (7) The resin-coated stainless steel foil for an electricity storage device container according to any one of the above.

  Even if the temperature cycling test essential for the electricity storage device is imposed, the present invention maintains a strong adhesive force on the outer surface of the container on the entire surface of the laminate, does not peel off, and does not contain dust or foreign matter. It is possible to provide a resin-coated stainless steel foil for an electricity storage device container having excellent properties, and contribute to improving the reliability of the electricity storage device.

It is a cross-sectional schematic diagram which shows an example of the resin-coated stainless steel foil of this invention.

  Hereinafter, the present invention will be described in detail.

  First, the resin composition (A) used in the present invention is a resin composition containing 50% by mass or more of one or more selected from polyolefins, polyesters, polyamides, and polyimides. These resin compositions are preferable as materials to be laminated on the outside of the electricity storage device container from the viewpoints of mass productivity, insulation, mechanical properties such as workability and scratch resistance, and chemical stability.

The polyolefin used in the present invention is a resin composition mainly composed of a resin having a repeating unit of the following (formula 1). The main component is that the resin having the repeating unit of (Formula 1) constitutes 50% by mass or more.
-CR ¹ H-CR ² R ^3- (Formula 1)
(Wherein R ¹ and R ² each independently represents an alkyl group having 1 to 12 carbon atoms or hydrogen, and R ³ represents an alkyl group having 1 to 12 carbon atoms, an aryl group or hydrogen)
The polyolefin used in the present invention may be a homopolymer of these structural units or two or more types of copolymers. It is preferable that five or more repeating units are chemically bonded. If it is less than 5, the polymer effect is difficult to exert. Examples of repeating units include repeating units appearing when addition polymerization of terminal olefins such as propene, 1-butene, 1-pentene, 4-methyl-1pentene, 1-hexene, 1-octene, 1-decene, 1-dodecene, etc. In addition to aliphatic olefins such as repeating units when isobutene is added, and styrene monomer, o-methylstyrene, m-methylstyrene, p-methylstyrene, o-ethylstyrene, m-ethylstyrene, o-ethyl Aromatic olefins such as styrene monomer addition polymer units such as alkylated styrene such as styrene, ot-butylstyrene, m-t-butylstyrene, pt-butylstyrene, halogenated styrene such as monochlorostyrene, and terminal methylstyrene Is mentioned. For example, low density polyethylene, medium density polyethylene, high density polyethylene, linear low density polyethylene, cross-linked polyethylene, polypropylene, polybutene, polypentene, polyhexene, polyoctenylene, polyisoprene, polybutadiene, which are homopolymers of terminal olefins Etc. Examples of the copolymer of the above unit include ethylene-propylene copolymer, ethylene-butene copolymer, ethylene-propylene-hexadiene copolymer, ethylene-propylene-5-ethylidene-2-norbornene copolymer, etc. Aliphatic polyolefins, aromatic polyolefins such as styrene copolymers, and the like, but are not limited thereto, as long as the above repeating units are satisfied. Further, it may be a block copolymer or a random copolymer. These resins may be used alone or in combination of two or more.

  Most preferable from the viewpoints of handling properties and barrier properties of corrosion-causing substances are low density polyethylene, medium density polyethylene, high density polyethylene, linear low density polyethylene, cross-linked polyethylene, polypropylene or a mixture of two or more of these.

  In addition, the polyolefin according to the present invention only needs to have the olefin unit as a main component, and a vinyl monomer, a polar vinyl monomer, and a diene monomer, which are substitutes of the unit, are copolymerized in a monomer unit or a resin unit. Also good. The copolymer composition is 50% by mass or less, preferably 30% by mass or less, based on the above unit. If it exceeds 50% by mass, properties as an olefin resin such as a barrier property against a causative substance may be deteriorated. Examples of polar vinyl monomers include acrylic acid derivatives such as acrylic acid, methyl acrylate and ethyl acrylate, methacrylic acid derivatives such as methacrylic acid, methyl methacrylate and ethyl methacrylate, acrylonitrile, maleic anhydride and maleic anhydride. Examples thereof include imide derivatives and vinyl chloride.

  The polyester according to the present invention includes only hydroxycarboxylic acid compound residues, dicarboxylic acid residues and diol compound residues, or hydroxycarboxylic acid compound residues and dicarboxylic acid residues and diol compound residues. Each is a thermoplastic polyester as a constituent unit. Moreover, these mixtures may be sufficient.

  Examples of hydroxycarboxylic acid compounds used as raw materials for hydroxycarboxylic acid compound residues include p-hydroxybenzoic acid, p-hydroxyethylbenzoic acid, 2- (4-hydroxyphenyl) -2- (4′-carboxyphenyl) propane These may be used alone or in combination of two or more.

  Examples of dicarboxylic acid compounds that form dicarboxylic acid residues include terephthalic acid, isophthalic acid, orthophthalic acid, 1,4-naphthalenedicarboxylic acid, 2,3-naphthalenedicarboxylic acid, 2,6-naphthalenedicarboxylic acid, 2 , 7-Naphthalenedicarboxylic acid, diphenic acid, diphenyldicarboxylic acid, diphenoxyethanedicarboxylic acid and other aromatic dicarboxylic acids and adipic acid, pimelic acid, sebacic acid, azelaic acid, decanedicarboxylic acid, malonic acid, succinic acid, malic acid And aliphatic dicarboxylic acids such as citric acid, and alicyclic dicarboxylic acids such as cyclohexanedicarboxylic acid. These may be used alone or in admixture of two or more.

  Next, diol compounds that form diol residues are exemplified by 2,2-bis (4-hydroxyphenyl) propane (hereinafter abbreviated as “bisphenol A”), bis (4-hydroxyphenyl) methane, bis ( 2-hydroxyphenyl) methane, o-hydroxyphenyl-p-hydroxyphenylmethane, bis (4-hydroxyphenyl) ether, bis (4-hydroxyphenyl) sulfone, bis (4-hydroxyphenyl) sulfide, bis (4-hydroxy Phenyl) ketone, bis (4-hydroxyphenyl) diphenylmethane, bis (4-hydroxyphenyl) -p-diisopropylbenzene, bis (3,5-dimethyl-4-hydroxyphenyl) methane, bis (3-methyl-4-hydroxy) Phenyl) methane, bis (3,5-dimethyl-4-hydroxyphenyl) ether, bis (3,5-dimethyl-4-hydroxyphenyl) sulfone, bis (3,5-dimethyl- 4-hydroxyphenyl) sulfide, 1,1-bis (4-hydroxyphenyl) ethane, 1,1-bis (3,5-dimethyl-4-hydroxyphenyl) ethane, 1,1-bis (4-hydroxyphenyl) Cyclohexane, 1,1-bis (4-hydroxyphenyl) -3,3,5-trimethylcyclohexane, 1,1-bis (4-hydroxyphenyl) -1-phenylethane, bis (4-hydroxyphenyl) phenylmethane, 2,2-bis (4-hydroxyphenyl) propane, 2,2-bis (4-hydroxyphenyl) butane, 2,2-bis (3,5-dimethyl-4-hydroxyphenyl) propane, 2,2-bis (3,5-dichloro-4-hydroxyphenyl) propane, 2,2-bis (3,5-dibromo-4-hydroxyphenyl) propane, 2,2-bis (3-methyl-4-hydroxyphenyl) propane, 2,2-bis (3-chloro-4-hydroxyphenyl) propane, 2,2-bis (3-bromo-4-hydroxyphenyl) propane, 1,1,1,3,3,3-he Safluoro-2,2-bis (4-hydroxyphenyl) propane, 4,4'-biphenol, 3,3 ', 5,5'-tetramethyl-4,4'-dihydroxybiphenyl, 4,4'-dihydroxybenzophenone Aromatic diols such as ethylene glycol, trimethylene glycol, propylene glycol, tetramethylene glycol, 1,4-butanediol, pentamethylene glycol, neopentyl glycol, hexamethylene glycol, dodecamethylene glycol, diethylene glycol, triethylene glycol, tetra Examples include ethylene glycol, polyethylene glycol, aliphatic diols such as hydrogenated bisphenol A, and alicyclic diols such as cyclohexanedimethanol. These can be used alone or in combination of two or more. You can also. In addition, the polyester resins obtained from these may be used alone or in combination of two or more.

  The polyester according to the present invention may be composed of these compounds or a combination thereof, and among them, an aromatic polyester resin composed of an aromatic dicarboxylic acid residue and a diol residue is preferable for workability, heat From the viewpoint of mechanical stability.

  The polyester according to the present invention is a small amount of structural units derived from polyfunctional compounds such as trimesic acid, pyromellitic acid, trimethylolethane, trimethylolpropane, trimethylolmethane, pentaerythritol, for example, an amount of 2 mol% or less. May be included.

  From the viewpoint of heat resistance and processability, the most preferable combination of these dicarboxylic acid compounds and diol compounds is a dicarboxylic acid compound of terephthalic acid 50 to 95 mol%, isophthalic acid and / or orthophthalic acid 50 to 5 mol%. , A combination of 2 to 5 carbon glycols with diol compounds.

  Examples of preferred polyesters according to the present invention include polyethylene terephthalate, polybutylene terephthalate, polyhexamethylene terephthalate, polycyclohexylene dimethylene terephthalate, polyethylene-2,6-naphthalate, polybutylene-2,6-naphthalate, etc. Among these, polyethylene terephthalate, polybutylene terephthalate, polyethylene-2,6-naphthalate, and polybutylene-2,6-naphthalate having appropriate mechanical properties, gas barrier properties, and metal adhesion are most preferable.

  The polyamide according to the present invention is an aliphatic polyamide resin, and is an aromatic polyamide resin such as polyhexamethylenediamine terephthalamide, polyhexamethylenediamine isophthalamide, xylene group-containing polyamide, and a modified product thereof or a mixture thereof. Etc. Specific examples include nylon 6, nylon 6,6, nylon 6,10, nylon 6,12, nylon 11, nylon 12, and nylon 4,6. Examples thereof include nylon 6, nylon 66, nylon 69, nylon 46, nylon 610, nylon 12, polymetaxylene adipamide, and those obtained by copolymerizing or blending these components.

  The polyimide according to the present invention is a general polyimide resin, a polyimide resin produced by reacting a diamine compound with benzene-1,2,4,5-tetracarboxylic anhydride, and an imide group in the structure. A resin made of polymer. Specific examples include polyimide, polyamideimide, polyetherimide, polysiloxaneimide, polybenzimidazoleimide and the like.

  In the resin composition (A), polyester is particularly preferable because of excellent balance of chemical resistance, heat resistance, processability, and price.

  Further, the resin composition (A) used in the present invention includes an antioxidant, a heat stabilizer, a light stabilizer, a release agent, a lubricant, a pigment, a flame retardant, a plasticizer, and an antistatic agent depending on the purpose. It is also possible to add an appropriate amount of antibacterial and antifungal agents.

  The resin composition (A) used in the present invention may be a single layer or a plurality of layers. A plurality of layers coated with different resins such as polyolefin, polyester, polyamide, and polyimide may be used.

  Whether the resin composition (A) is a single layer or a plurality of layers, the total thickness is preferably in the range of 5 to 200 μm, more preferably in the range of 10 to 100 μm. If it is less than 5 μm, functions such as processability, design, and insulation may not be sufficiently imparted, and if it is thicker than 200 μm, processability may be deteriorated. There are no economic benefits. In addition, since the resin composition (A) is the outermost surface of the electricity storage device container, an acrylic film or the like is laminated on the opposite surface to which the adhesive (B) is applied to improve weather resistance, or hard coat Laminate film or apply hard coat agent to improve surface hardness, provide printing layer to improve design, apply corona treatment to improve printability, or flame retardant, plastic, charged An antibacterial and antifungal layer can also be laminated.

  Next, the adhesive (B) used in the present invention is not particularly limited as long as it exhibits adhesive force by heating. If it is an adhesive that develops adhesive force by heating, it has the effect of buffering the stress strain caused by the difference in thermal expansion and contraction between the resin composition (A) and the stainless steel foil on the entire adhesive surface, and heat laminated. An effect of suppressing peeling of the resin composition (A) is obtained. Examples of the adhesive that exhibits an adhesive force by heating include adhesives such as a thermoplastic resin type such as hot melt, a thermosetting resin type, and a two-component mixed thermoadhesive type. The temperature for developing the adhesive force may be lower than the melting point of the resin composition (A), but is preferably 10 ° C. or more lower than the melting point. In general, the temperature at which the adhesive force is expressed is preferably 400 ° C. or lower.

  An adhesive that develops an adhesive force when heated is an anchoring effect (anchor effect) in which the adhesive enters into the irregularities on the surface of the stainless steel foil when heated, or / and a hydrogen bond or an ionic bond depending on the polarity of the functional group, or / In addition, it is possible to use a thermosetting resin, a thermoplastic resin, a reactive resin composition, etc., in order to exert an adhesive force by a covalent bond or the like by a chemical reaction. Those containing an isocyanate group, an amide group, an epoxy group, a phenol group, a carbonyl group, an acid anhydride group, and the like are preferable. Urethane-based, epoxy-based, phenol-based, nylon-based, or unsaturated polyester-based adhesives are preferable from the viewpoint of application to the resin composition, availability, and cost. Further, from the viewpoint of adhesion to the stainless steel foil and the resin composition (A) and flexibility as a buffer layer, urethane, nylon and unsaturated polyester adhesives are more preferable.

  The urethane-based adhesive is not particularly limited as long as it is an adhesive having an isocyanate group, and may be any of a thermosetting adhesive, a thermoplastic adhesive, and the like. Methylene-bis (p-phenylene diisocyanate), hexamethylene diisocyanate, 1,6-hexamethylene diisocyanate, 2,4-tolylene diisocyanate, toluene diisocyanate, 1-chlorophenyl diisocyanate, 1,5-naphthylene diisocyanate, thiodipropyl diisocyanate And an adhesive containing ethylbenzene-α-2-diisocyanate, 4,4 ′, 4 ″ -triphenylmethane triisocyanate, and the like. Urethane adhesive achieves good adhesion by the interaction between isocyanate group and hydroxyl group on the surface of stainless steel foil, and the anchoring effect (anchor effect) that the adhesive enters the irregularities on the surface of the stainless steel foil. It also adheres well to the composition (A) and has appropriate flexibility as a stress buffer layer.

  The epoxy adhesive is not particularly limited as long as it is an adhesive having an epoxy group, but is generally a thermosetting resin. Specifically, bisphenol A and epichlorohydrin can be used. Examples thereof include a bisphenol type reacted in the presence of an alkali and other novolak types. Epoxy adhesives achieve good adhesion due to the interaction between epoxy groups, glycidyl groups, etc. and hydroxyl groups on the surface of stainless steel foil, and the anchoring effect (anchor effect) that allows the adhesive to enter the irregularities on the surface of the stainless steel foil. And also adheres well to the resin composition (A).

  The phenolic adhesive is not particularly limited as long as it is an adhesive having a phenolic compound, but is generally a thermosetting resin. Specifically, phenol reacts with formaldehyde. And an adhesive containing resol, resistol, regit, novolak and the like cured with hexamethylenetetramine or the like.

  The nylon adhesive may be any adhesive having an amide group and is not particularly limited, and may be any of a thermosetting adhesive, a thermoplastic adhesive, and the like. Nylon 6, Nylon 6,6, Nylon 6,10, Nylon 6,12, Nylon 11, Nylon 12, Nylon 4,6. Examples thereof include nylon 6, nylon 66, nylon 69, nylon 46, nylon 610, nylon 12, polymetaxylene adipamide, and those obtained by copolymerizing or blending these components. Nylon-based adhesives achieve good adhesion due to the interaction between the amide group and the hydroxyl group on the surface of the stainless steel foil, and the anchoring effect (anchor effect) that allows the adhesive to enter the irregularities on the surface of the stainless steel foil. It also adheres well to the composition (A) and has appropriate flexibility as a stress buffer layer.

  The unsaturated polyester adhesive is not particularly limited as long as it is a polyester having an unsaturated group, but is generally a thermoplastic resin type, but is a thermosetting type using a crosslinking agent. Specific examples include those obtained by polycondensation of an unsaturated basic acid such as maleic anhydride and a polyhydric alcohol such as ethylene glycol. These adhesives may be used alone or in combination of two or more. Unsaturated polyester adhesives achieve good adhesion due to the interaction between carbonyl groups, etc. and the hydroxyl groups on the surface of the stainless steel foil, and the anchoring effect (anchor effect) that allows the adhesive to enter the irregularities on the surface of the stainless steel foil. In addition, it also adheres well to the resin composition (A) and has appropriate flexibility as a stress buffer layer.

  Further, the adhesive (B) used in the present invention includes a curing agent, a curing catalyst, a flexibility imparting agent, a filler, a diluent, a heat stabilizer, a light stabilizer, a pigment, and a flame retardant according to the purpose. It is also possible to add an appropriate amount of a plasticizer, an antistatic agent, an antibacterial antifungal agent or the like.

  The method of applying the adhesive (B) to the resin composition (A) is not particularly limited, but specific examples include (1) melting the adhesive (B) with an extruder with a T die. A method of kneading into a film and thermocompression bonding to the resin composition (A) immediately after extrusion. In this case, simultaneous extrusion of a plurality of layers may be performed. (2) A method of coating the resin composition (A) with a bar coater, roll coater, spin coater, spray or the like after the adhesive (B) is melted or dissolved in a solvent. (3) A method in which a sheet or film obtained by extruding or molding the adhesive (B) in advance is thermocompression bonded to the resin composition (A). In this case, the film may be stretched uniaxially or biaxially or may be laminated in a plurality of layers. (4) It can be applied by a method of immersing the resin composition (A) in an adhesive (B) melted or dissolved in a solvent. Among these, the methods (1) and (2) are preferable from the viewpoint of work efficiency.

The thickness of applying the adhesive (B) to the resin composition (A) is not particularly limited, but the thickness (t _a ) of the resin composition (A) and the thickness of the adhesive (B) (t _b in), it is preferable t _b / t _a is 0.01 to 0.5. If it is 0.01 or less, the adhesive strength with the stainless steel foil is insufficient and peeling is likely to occur, and if it is more than 0.5, the adhesive protrudes due to thermal lamination or the surface of the resin composition (A) after coating is dented. Defects are likely to be caused, and when the adhesive gels for some reason, it becomes a large lump and easily becomes a foreign matter.

The tensile modulus of the tensile modulus of the resin composition _(A) (E _a) and the adhesive (B) in (E _b), it is preferable that E _a / E _b> 1. When Ea / Eb ≦ 1, the role of the adhesive (B) for buffering the stress strain between the resin composition (A) and the stainless steel foil is weakened, and peeling is likely to occur. The tensile elastic modulus was measured by JIS K7127 after molding the resin composition (A) and the adhesive (B) to a proper thickness in a film or sheet.

  The stainless steel foil according to the present invention may be any of austenite (SUS301, 304, 316, etc.), ferrite (SUS430, etc.), martensite (SUS410, etc.), and heat treatment and rolling can be performed freely. From the viewpoint of processability and strength as a container, the thickness is preferably 200 μm or less and 10 μm or more.

The surface of the stainless steel foil used in the present invention may be pretreated. By performing the base treatment, the chemical adhesion between the adhesive (B) and the stainless steel foil can be increased. Specifically, a method for removing oil from the surface of the stainless steel foil and removing the scale as necessary, or performing a chemical conversion treatment thereafter is given as the base treatment. Examples of scale removal treatment methods include pickling, sand blast treatment, grid blast treatment, etc., and chemical conversion treatment methods include chromate treatment, non-chromate treatment without using Cr ⁺⁶ , strike plating treatment, epoxy primer treatment, and silane coupling treatment. And titanium coupling treatment.

  In FIG. 1, the structural example of the resin coating stainless steel foil for electrical storage device containers of this invention is shown. Although FIG. 1 is a cross-sectional view, in this example, the resin composition (A) is heat-laminated via an adhesive (B) on the outer surface of the stainless steel foil 1 container. The surface is subjected to a surface treatment 4 such as chromate, and a resin composition such as polyethylene or polypropylene is formed by thermal lamination or other methods.

  The method of coating the stainless steel foil with the resin composition (A) obtained by applying the adhesive (B) is not particularly limited as long as it is a heat laminate that is heated and pressure-bonded. In order to enhance the physical and chemical interaction with the stainless steel foil by increasing the contact area, the melting point of the adhesive (B), the curing start temperature Alternatively, it is preferable that the stainless steel foil is heated to an adhesion start temperature or higher and 400 ° C. or lower, bonded to the resin composition (A) coated with the adhesive (B), and pressed. More preferably, thermal lamination is performed at a melting point of the adhesive (B), a curing start temperature, or a temperature 10 ° C. higher than the adhesion start temperature and not higher than the melting point of the resin composition (A). The cleanliness around the device is preferably class 10000 or less.

The resin laminated on the inner surface of the container is not particularly limited, but a resin composition (C) containing 50% by mass or more of the above-mentioned polyolefin and having a thickness of 10 μm to 150 μm is preferable. If it is 10 μm or less, the strength of the seal part when the container is formed by heat sealing is insufficient, and if it is 150 μm or more, moisture permeation from the seal part becomes large, which tends to adversely affect the electricity storage device. The laminating method is not particularly limited, and existing techniques such as thermal lamination, dry lamination, and wet lamination can be used. Moreover, the same surface treatment as that on the outer surface side of the container may be applied to the surface of the stainless steel foil. In this case, preferable treatment includes chromate treatment, non-chromate treatment without using Cr ^+6, and the like.

  In addition, the method for forming the stainless steel foil into a container shape is not particularly limited, and conventional methods such as pressing, ironing, and drawing can be used. The shape of the container is not particularly limited, such as a rectangular parallelepiped rectangular tube shape or a cylindrical shape. Further, in use as a container, it is preferable to seal the lid and the bottom together. At this time, stainless steel foils squeezed by pressing or the like may be bonded together, or only one of them may be squeezed. Further, as a method of sealing, a conventional bonding method can be used, and specifically, a method of bonding using an adhesive, a method of bonding by heat fusion by heat sealing, and the like are specifically limited. Although not intended, heat sealing is preferred in terms of manufacturability. In the case of heat sealing, it is preferable to match the surfaces on which the resin composition (C) is laminated.

  Next, the present invention will be described more specifically based on examples and comparative examples, but the present invention is not limited to the following examples.

  All the stainless steel foils used in this example and comparative example were SUS304BA having a thickness of 50 μm.

  In Examples 1, 4 to 14, and 16 to 22, a nylon-based adhesive (Daiamide 470-1 manufactured by Daicel Degussa Co., Ltd.) was dissolved in a mixed solvent having a mass ratio of cresol and xylene of 70:30 at a concentration of 15% by mass. Then, it was applied to the resin composition (A) so that the film thickness after drying was 1 μm. The adhesive side was in contact with the stainless steel foil, and the stainless steel foil was heated to the temperature indicated in the laminating temperature column, and was thermocompression bonded to the stainless steel foil at a pressure of 1 MPa.

  In Example 2, a urethane-based adhesive (Nipporan 3022 manufactured by Nippon Polyurethane Industry Co., Ltd.) was applied to the resin composition (A) so that the film thickness after drying was 1 μm. The adhesive side was in contact with the stainless steel foil, and the stainless steel foil was heated to 200 ° C. and thermocompression bonded to the stainless steel foil at a pressure of 1 MPa, and heat laminated.

  In Example 3, as an unsaturated polyester-based adhesive, 2.0% by mass of ethylene glycol, 51.0% by mass of hexahydrophthalic anhydride, 47.0% by mass of glycidyl methacrylate, 0.9% by mass of N, N-dimethylbenzylamine, and hydroquinone A solution prepared by mixing 0.2% by mass and 20% by mass of ethyl acetate was reacted at 80 ° C. for 10 hours, and this was cooled and dissolved in ethyl acetate to a concentration of 20% by mass. After drying, the film thickness was 1 μm. It applied to the resin composition (A) so that it might become. The adhesive side was in contact with the stainless steel foil, and the stainless steel foil was heated to 200 ° C. and thermocompression bonded to the stainless steel foil at a pressure of 1 MPa, and heat laminated.

  In Example 15, an epoxy adhesive (EM-150 manufactured by Nagase ChemteX Corporation) was applied to the resin composition (A) so that the film thickness after drying was 1 μm. The adhesive side was in contact with the stainless steel foil, and the stainless steel foil was heated to 200 ° C. and thermocompression bonded to the stainless steel foil at a pressure of 1 MPa, and heat laminated.

In Comparative Examples 1 and 4, dry lamination was performed with a dry laminating adhesive (AD502 / CAT10 manufactured by Toyo Morton Co., Ltd.) applied at 4 g / m ² . In Comparative Example 2, the wet laminate adhesive (Sumitomo Seika Co., Ltd., Syxen A) was applied at a dry coating amount of 2 g / m ² , and the stainless steel foil and the resin composition (A) were bonded together and dried. did. In Comparative Example 3, the resin composition (A) was heat-laminated by heating the stainless steel foil to 250 ° C. and directly thermocompression bonding to the stainless steel foil at a pressure of 1 MPa.

  As the resin composition (A), in Examples 1 to 3, 7, 9, 11 to 18, 21, 22 and Comparative Examples 1 to 3, a stretched polyethylene terephthalate film (Teflex manufactured by Teijin DuPont Films Ltd., hereinafter referred to as stretched PET) In Examples 8 and 10, the stretched PET was heated to 150 ° C. using a biaxial stretching test apparatus manufactured by Toyo Seiki Seisakusho Co., Ltd. What was stretched and formed to have a thickness of 5 μm, 3 μm, stretched nylon film in Example 4 (Harden N1100 manufactured by Toyobo Co., Ltd., hereinafter stretched nylon), stretched polypropylene film in Example 5 ( In the examples 6, 19, and 20, polyimide films (Kapton 50H / V, hereinafter referred to as polyimide) manufactured by Toray DuPont Co., Ltd. were respectively used. In Comparative Example 4, a melamine resin sheet (Dai Nippon Printing Co., Ltd. melamine-based resin FRP prepreg sheet, hereinafter referred to as melamine) was pressed at a pressure of 200 ° C. and 2 MPa to form a thin film with a thickness of 50 μm. A).

  In Example 21, on the resin composition (A), a hard coat agent (SSG HB31B manufactured by Nitto Boseki Co., Ltd.) was applied using a bar coater so that the film thickness after drying was 5 μm, and the humidity was 25 ° C. It was cured in a 60% room for 3 days and used as a coating layer.

In Example 22, chromate treatment was applied to the inner surface side of the container, and a modified polypropylene film (Admer QE060C # 50 manufactured by Tosero Co., Ltd.) having a thickness of 50 μm was thermocompression bonded to the stainless steel foil at a pressure of 175 ° C. and 1 MPa. . Chromate treatment is performed by adding phosphoric acid, hydrochloric acid, ammonium fluoride, etc. to a room temperature bath consisting of 25 g / L of chromic anhydride, 3 g / L of sulfuric acid, 4 g / L of nitric acid, and a cathode current density of 25 A / dm ² , A chromate treatment layer was formed by energizing for 15 seconds.

  The tensile elastic modulus was measured according to JIS K7127, and the magnitudes of Ea and Eb were compared.

  The production conditions for these examples and comparative examples are shown in Table 1, and the evaluation results are shown in Table 2.

  Temperature cycle peeling distance is the progress of edge peeling after 6 hours of temperature cycling test in which the resin-coated stainless steel foil was heated and held at 80 ° C for 15 minutes, cooled and held at -40 ° C for 15 minutes. The distance was measured. The smaller one is preferable, and 0.5 mm or less was regarded as acceptable.

  In the appearance inspection, the produced resin-coated stainless steel foil was pressed, visually inspected, and evaluated according to the following criteria. A: No problem, B: Surface dent or adhesive protruding, C: Surface dent and adhesive protruding both, D: Adhesive failure due to dust / foreign matter mixing or missing adhesive . A is the most preferable, and C or more is considered acceptable.

  The press work is a rectangular tube container-shaped drawing often used as an electricity storage device container, and the conditions are a die 142 mm x 142 mm, corner R diameter 4 mm, punch 140 mm x 140 mm, corner R diameter 4 mm, wrinkle holding force 6 tons, The lubricant used was a mixture of Johnson WAX122 and machine oil 1: 1, with a press speed of 60 mm / min, a blank size of 200 mm x 200 mm, and a depth of 5 mm.

In Example 22, two of these press-formed molded products were combined, and an electrolytic copper foil coated with graphite as a negative electrode material, a separator, and an aluminum foil coated with LiNiCo _0.15 Al _0.05 O ₂ as a positive electrode material Sequentially laminated, electrolyte solution (1MLiPF6 EC / DEC-1 / 1 manufactured by Toyama Pharmaceutical Co., Ltd.) is injected into this, vacuum sealed under heat seal conditions of 200 ° C, 0.4 MPa, 10 seconds, and lithium ion secondary A battery was produced. This battery was subjected to an initial charge / discharge characteristic evaluation test and a charge / discharge cycle characteristic evaluation test. In the initial charge / discharge characteristic evaluation test, the first charge was performed at 25 ° C., and the discharge was performed immediately after that to measure the ratio between the charge capacity and the discharge capacity. In the charge / discharge cycle characteristic evaluation test, the ratio between the discharge capacity and the initial discharge capacity after 300 charge / discharge cycles at 25 ° C. was measured, and 80% or more was determined to be acceptable.

  Both of the results of the initial charge / discharge characteristic evaluation test and the charge / discharge cycle characteristic evaluation test of the battery produced in Example 22 were 80% or more, and it was confirmed that the battery operates properly.

  According to the above Examples 1 to 22 and Comparative Examples 1 to 4, the stainless steel foil of the present invention is thinned to increase the electric capacity that cannot be achieved with the aluminum foil that is the mainstream of conventional metal foils for power storage device containers. In addition, despite the use of stainless steel foil that achieves both strength improvement for safety improvement, even if the temperature cycling test required for the electricity storage device is imposed, the entire laminate surface has a strong adhesive force on the outer surface of the container. It was confirmed that it was excellent in cleanness and design, without being kept and peeled off, without being mixed with dust and foreign matter.

Claims (8)

  A resin-coated stainless steel foil obtained by laminating a resin on both surfaces of a stainless steel foil, and when processed into an electricity storage device container, the adhesive force is expressed by heating on the surface of the stainless steel foil that is the outside of the container Through the adhesive (B) layer, the resin composition (A) layer containing one or more resins selected from polyolefin, polyester, polyamide, and polyimide in total of 50% by mass or more is laminated by thermal lamination. A resin-coated stainless steel foil for a power storage device container. The resin composition the ratio (t _b / t _a) of (A) layer having a thickness (t _a) and the adhesive (B) layer thickness (t _b), the power storage according to claim 1, wherein 0.01 to 0.5 Resin-coated stainless steel foil for device containers. The resin composition is tensile modulus (A) layer (E _a) and the adhesive tensile modulus (B) layer ratio _{(E b) (E a /} E b), in E _a / E _b> 1 3. The resin-coated stainless steel foil for an electricity storage device container according to claim 1 or 2.   4. The resin-coated stainless steel foil for an electricity storage device container according to claim 1, wherein the resin composition (A) is a resin containing 50% by mass or more of polyester.   The electricity storage device container according to any one of claims 1 to 4, wherein the adhesive (B) is one or more selected from urethane resins, epoxy resins, nylon resins, and unsaturated polyester resins. Resin coated stainless steel foil. 6. The resin-coated stainless steel foil for an electricity storage device container according to claim 1, wherein the thickness (t _a ) of the resin composition (A) layer is 5 μm or more and 200 μm or less.   7. The resin-coated stainless steel foil for an electricity storage device container according to claim 1, further comprising a coating layer on the resin composition (A) layer.   The resin laminated on the surface of the stainless steel foil that is the inside of the electricity storage device container is a resin composition (C) containing 50% by mass or more of polyolefin, and the thickness thereof is 10 μm or more and 150 μm or less. A resin-coated stainless steel foil for an electricity storage device container according to claim 1.

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