JP5704202B2 - Battery packaging materials - Google Patents

Description

  The present invention relates to a resin composition that can impart high insulating properties, sealing properties, and moldability to a battery packaging material when used in a sealant layer of the battery packaging material.

  Conventionally, various types of batteries have been developed. In any battery, a packaging material is an indispensable member for sealing battery elements such as electrodes and electrolytes. Conventionally, metal packaging materials have been widely used as battery packaging, but in recent years, with the increasing performance of electric vehicles, hybrid electric vehicles, personal computers, cameras, mobile phones, etc., batteries are required to have various shapes. At the same time, there is a demand for reduction in thickness and weight. However, metal battery packaging materials that have been widely used in the past have the disadvantages that it is difficult to follow the diversification of shapes and that there is a limit to weight reduction.

  Therefore, in recent years, as a battery packaging material that can be easily processed into various shapes and can be reduced in thickness and weight, a film-like laminate in which a base layer / adhesive layer / metal layer / sealant layer are sequentially laminated. Has been proposed (see, for example, Patent Document 1). Such a film-shaped battery packaging material is formed so that the battery element can be sealed by causing the sealant layers to face each other and heat-sealing the peripheral portion by heat sealing.

  For example, Patent Document 1 discloses a battery case including a biaxially stretched polyamide film layer as an outer layer, an unstretched thermoplastic resin film layer as an inner layer, and an aluminum foil layer disposed between the two film layers. A packaging material is disclosed.

  Conventionally, in such a battery packaging material, polypropylene or the like is generally used as a resin for forming a sealant layer in consideration of the electrolytic solution resistance, seal strength, and the like. Since polypropylene has a melting point of 120 ° C. or higher, it has the advantage of having high sealing strength even when the battery packaging material is exposed to high temperatures.

  Polypropylene has a crystalline part and an amorphous part, and the melting point decreases as the amorphous part increases, and the melting point increases as the crystalline part increases. For example, when polypropylene having a large amount of amorphous part is used for the sealant layer, there is a problem that, for example, thermal melting starts at about 80 ° C. and the sealing strength becomes insufficient when the battery temperature rises. On the other hand, when polypropylene with many crystal parts is used for the sealant layer, the melting point becomes high, so that the seal strength at high temperature is increased, but the crystallinity control in the cooling process after heat sealing (for example, the growth of crystal nuclei) Control of increase in the number of crystal nuclei, etc.) is difficult. For this reason, for example, when the seal portion is bent after heat sealing, there is a problem that cracks are generated in the seal portion of the sealant layer or in the vicinity thereof, and the insulating property is likely to be lowered.

  In order to solve such problems, for example, after heat sealing using a polypropylene having a high melting point and a high melting point for the sealant layer, a cooling process is performed in which a cooling plate is pressed against the sealing portion or cooling air is blown. There is also. However, even when such a cooling step is provided, it is not easy to suppress the occurrence of cracks in the seal portion. Furthermore, since battery packaging materials are required to have not only insulating properties but also high sealing properties and moldability, it is also required to impart these properties to the resin forming the sealant layer.

JP 2008-287971 A

  Under such circumstances, the present invention suppresses the occurrence of cracks when the heat-sealed seal part of the battery packaging material is bent when used in the sealant layer of the battery packaging material. Has high sealing strength even when exposed to high temperatures or electrolytes, and has high insulation properties for battery packaging materials by suppressing the occurrence of cracks when stretched during molding of battery packaging materials. The main object of the present invention is to provide a resin composition capable of imparting sealing properties and moldability. Another object of the present invention is to provide a battery packaging material using the resin composition as a sealant layer.

  The present inventor has intensively studied to solve the above problems. As a result, (A-1) a random copolymer of propylene-ethylene having a melting point of 156 ° C. or higher and an ethylene content of 5% by mass or less, and (A -2) A resin composition comprising at least one of a propylene-ethylene block copolymer having a melting point of 158 ° C or higher and an ethylene content of 7% by mass or less, and (B) a polyolefin elastomer having a melting point of 135 ° C or higher. In addition, when used in a sealant layer for battery packaging materials, it is possible to suppress the generation of cracks when bending the heat-sealed seal portion of the battery packaging material, and to provide high insulation, and the seal portion has a high temperature. Or, when exposed to electrolyte solution, it has high sealing strength and can provide high sealing performance, and suppresses the generation of cracks when battery packaging materials are stretched. It was found to be able to impart formability have. The present invention has been completed by further studies based on such knowledge.

That is, this invention provides the invention of the aspect hung up below.
Item 1. (A-1) a random copolymer of propylene-ethylene having a melting point of 156 ° C. or higher and an ethylene content of 5% by mass or less, and (A-2) a melting point of 158 ° C. or higher and an ethylene content of 7% by mass or less. At least one of a propylene-ethylene block copolymer;
(B) a polyolefin-based elastomer having a melting point of 135 ° C. or higher;
A resin composition for a sealant layer of a battery packaging material.
Item 2. Item 2. The resin composition according to Item 1, wherein the content of the (B) polyolefin elastomer having a melting point of 135 ° C or higher is 20 to 75 mass%.
Item 3. (A-1) a random copolymer of propylene-ethylene having a melting point of 156 ° C. or higher and an ethylene content of 5% by mass or less, and (A-2) a melting point of 158 ° C. or higher and an ethylene content of 7% by mass or less. Item 3. The resin composition according to Item 1 or 2, wherein the total content of the propylene-ethylene block copolymer is 25 to 80% by mass.
Item 4. Item 4. The resin composition according to any one of Items 1 to 3, further comprising a low stereoregular olefin having a weight average molecular weight of 10,000 or more, a mesopentad fraction (mmmm) of 90% or less, and a melting point of 70 ° C or more. object.
Item 5. Item 5. The resin composition according to any one of Items 1 to 4, wherein the (C) low stereoregular olefin comprises a 1-butene polymer.
Item 6. The content of the (B) polyolefin elastomer having a melting point of 135 ° C. or more is 20 to 65% by mass, the (C) weight average molecular weight is 10,000 or more, the mesopentad fraction (mmmm) is 90% or less, and the melting point is 70. Item 6. The resin composition according to any one of Items 1 to 5, wherein the content of the low stereoregular olefin that is at least ° C is 2 to 30% by mass.
Item 7. A battery packaging material comprising a laminate having at least a base material layer, a metal layer, and a sealant layer in this order,
The battery packaging material, wherein the sealant layer includes a layer formed of the resin composition according to any one of Items 1 to 6.
Item 8. A battery, wherein a battery element including a positive electrode, a negative electrode, and an electrolyte is sealed with the battery packaging material according to Item 7.

  According to the resin composition of the present invention, when used in the sealant layer of a battery packaging material, the occurrence of cracks when bending the heat-sealed seal part of the battery packaging material is suppressed, and the seal part Has high sealing strength even when exposed to high temperature or electrolytic solution, and suppresses the occurrence of cracks when the battery packaging material is stretched, so that the battery packaging material has high insulation, sealability, And formability can be imparted.

It is a schematic sectional drawing of the packaging material for batteries of this invention. It is a schematic sectional drawing of the packaging material for batteries of this invention.

  The resin composition of the present invention comprises (A-1) a random copolymer of propylene-ethylene having a melting point of 156 ° C. or higher and an ethylene content of 5% by mass or less, and (A-2) an ethylene having a melting point of 158 ° C. or higher. It contains at least one of a propylene-ethylene block copolymer having a content of 7% by mass or less and (B) a polyolefin elastomer having a melting point of 135 ° C. or higher. Hereinafter, the resin composition of the present invention, the battery packaging material using the resin composition for the sealant layer, and the battery will be described in detail.

1. Resin Composition The resin composition of the present invention is a resin composition used for, for example, a sealant layer of a battery packaging material as described later, and (A-1) has a melting point of 156 ° C. or higher and an ethylene content of 5 mass. % Propylene-ethylene random copolymer, and (A-2) at least one of propylene-ethylene block copolymer having a melting point of 158 ° C. or higher and an ethylene content of 7% by mass or less, and (B) melting point Includes a polyolefin-based elastomer having a temperature of 135 ° C. or higher.

  (A-1) Propylene-ethylene random copolymer having a melting point of 156 ° C. or higher and an ethylene content of 5% by mass or less (hereinafter sometimes simply referred to as “(A-1) random copolymer”) The melting point is 156 ° C. or higher, the proportion of ethylene in the (A-1) random copolymer is 5% by mass or less, and the constituent monomers propylene and ethylene are randomly polymerized. There is no particular limitation. (A-1) The melting point of the random copolymer can be adjusted by the molecular weight, the proportion of the crystalline portion, the proportion of propylene and ethylene, and the like. (A-1) As a random copolymer, a commercial item can also be used. Further, the upper limit of the melting point of the (A-1) random copolymer is not particularly limited as long as the effects of the present invention are exhibited, but preferably 165 ° C, more preferably 163 ° C. Further, the lower limit of the ethylene content in the (A-1) random copolymer is not particularly limited as long as the effects of the present invention are exhibited, but preferably 2% by mass. In addition, melting | fusing point of each component contained in the resin composition of this invention is a value measured with a differential scanning calorimeter (DSC).

  The content of the (A-1) random copolymer in the resin composition of the present invention is not particularly limited as long as the effects of the present invention are exhibited, but is preferably about 25 to 80% by mass, more preferably About 30-70 mass%, More preferably, about 33-65 mass% is mentioned.

  (A-2) Propylene-ethylene block copolymer having a melting point of 158 ° C. or higher and an ethylene content of 7% by mass or less (hereinafter sometimes simply referred to as “(A-2) block copolymer”) If melting point is 158 degreeC or more, the ratio of ethylene in the said (A-2) block copolymer is 7 mass% or less, and propylene and ethylene which are constituent monomers are block-polymerized. There is no particular restriction. (A-2) The melting point of the block copolymer can be adjusted by the molecular weight, the proportion of the crystalline portion, the proportion of propylene and ethylene, and the like. (A-2) As a block copolymer, a commercial item can also be used. (A-2) The upper limit of the melting point of the block copolymer is not particularly limited as long as the effects of the present invention are exhibited, but preferably 165 ° C, more preferably 163 ° C. In addition, the lower limit of the ethylene content in the (A-2) block copolymer is not particularly limited as long as the effect of the present invention is exhibited, but preferably 2% by mass.

  The content of the (A-2) block copolymer in the resin composition of the present invention is not particularly limited as long as the effects of the present invention are exhibited, but is preferably about 25 to 80% by mass, more preferably About 30-70 mass%, More preferably, about 33-65 mass% is mentioned.

  The total amount of (A-1) random copolymer and (A-2) block copolymer in the resin composition of the present invention is preferably about 25 to 80% by mass, more preferably 30 to 70. About mass%, More preferably, about 33-65 mass% is mentioned.

  (B) A polyolefin-based elastomer having a melting point of 135 ° C. or higher (hereinafter sometimes simply referred to as “(B) polyolefin-based elastomer”) has a melting point of 135 ° C. or higher and has characteristics as an elastomer (that is, If it is a polyolefin-type elastomer), it will not be restrict | limited in particular. (B) As a polyolefin-type elastomer, a propylene-type elastomer is mentioned preferably from viewpoints, such as an improvement of sealing strength and prevention of delamination after heat sealing. Examples of the propylene-based elastomer include polymers containing propylene and one or more α-olefins having 2 to 20 carbon atoms (excluding propylene) as constituent monomers, and the number of carbon atoms constituting the propylene-based elastomer is 2. Specific examples of the α-olefin of ˜20 (excluding propylene) include ethylene, 1-butene, 1-pentene, 1-hexene, 4-methyl-1-pentene, 1-octene, 1-decene, 1 -Dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicocene and the like. (B) A polyolefin-type elastomer may be used individually by 1 type, and may be used in combination of 2 or more type. In the resin composition of the present invention, a propylene-ethylene copolymer having both a specific melting point and an ethylene content, at least one of the (A-1) random copolymer and the (A-2) block copolymer. By blending the (B) polyolefin-based elastomer having a specific melting point with respect to the coalescence, the flexibility of the resin composition is improved, and when the resin composition is used for a sealant layer of a battery packaging material, Even when the heat-sealed seal portion of the battery packaging material is bent, high insulation can be imparted. In addition, by adding (B) a polyolefin-based elastomer, the sealing portion of the battery packaging material has high sealing strength even when exposed to high temperature or an electrolytic solution, so that excellent hermeticity can be imparted, Furthermore, since generation | occurrence | production of the crack when the packaging material for batteries is extended | stretched, the outstanding moldability can also be provided.

  (B) Melting | fusing point of polyolefin-type elastomer can be adjusted with molecular weight, the ratio of a crystalline part, the ratio of a propylene, and ethylene. (B) A commercial item can also be used as a polyolefin-type elastomer. (B) The upper limit of the melting point of the polyolefin-based elastomer is not particularly limited as long as the effect of the present invention is exhibited, but preferably 165 ° C, more preferably 163 ° C.

  The content of the (B) polyolefin-based elastomer in the resin composition of the present invention is not particularly limited as long as the effect of the present invention is achieved, but is preferably about 20 to 75% by mass, more preferably 25 to 70%. About mass%, More preferably, about 30-65 mass% is mentioned.

  In addition to (A-1) the random copolymer and (A-2) the block copolymer, and (B) the polyolefin-based elastomer, the resin composition of the present invention further includes (C) a weight average. A low stereoregular olefin having a molecular weight of 10,000 or more, a mesopentad fraction (mmmm) of 90% or less, and a melting point of 70 ° C. or more (hereinafter sometimes simply referred to as “(C) low stereoregular olefin”) It is preferable to include. When the resin composition of the present invention contains (C) a low stereoregular olefin, high flexibility can be imparted to the resin composition without substantially lowering the melting point of the resin composition. As a result, when the resin composition of the present invention is used for the sealant layer of the battery packaging material, the tensile yield point strength (MD + TD) of the battery packaging material described later can be lowered. The effect of making the pressure uniform becomes high, uniform sealing becomes possible, and high sealing performance is obtained. In addition, in resin cooling that occurs after heat sealing, the effect of suppressing the growth of crystal nuclei and the increase in the number of crystal nuclei in the resin composition is manifested, and fine cracks that occur due to increase in crystal nuclei after sealing and non-uniformization, etc. Can be prevented. For this reason, while being able to raise seal strength, it also becomes possible to suppress the permeability of the electrolyte solution which is the contents, and the stable sealing nature is obtained.

(C) As the low stereoregular olefin, if the weight average molecular weight is 10,000 or more, the mesopentad fraction (mmmm) is 90% or less, and the melting point is 70 ° C. or more, the effect of the present invention is achieved. It does not restrict | limit in particular as a limit, The well-known low stereoregular olefin which satisfies these physical properties can be used, and a commercial item can also be used. As the (C) low stereoregular olefin, for example, a polyolefin resin composition as disclosed in JP-A-2002-220503 can be used. (C) The weight average molecular weight of the low stereoregular olefin is preferably 30,000 or more. The mesopentad fraction (mmmm) is preferably 80% or less. As melting | fusing point, Preferably 75 degreeC or more is mentioned. Further, the upper limit value of the weight average molecular weight of the (C) low stereoregular olefin is not particularly limited as long as the effect of the present invention is exerted, and for example, about 1,000,000, preferably about 500,000 can be mentioned. The lower limit of the mesopentad fraction (mmmm) is not particularly limited as long as the effect of the present invention is exhibited, but may be 20%, for example, 35%. The upper limit of the melting point is not particularly limited as long as the effect of the present invention is exhibited, and examples thereof include 140 ° C., preferably 100 ° C. In the present invention, the weight average molecular weight is a value measured by gel permeation chromatography (GPC) using polystyrene as a standard sample. Further, in the present invention, the mesopentad fraction (mmmm) is determined according to “Polymer Journal, 16, 717 (1984)”, “Macromol. Chem. Phys., C29, 201 (1989)”, and “Macromol. Chem. Phys. , 198, 1257 (1997) ". That is, the mesopentad fraction is determined by measuring signals of methylene group and methine group using ¹³ C nuclear magnetic resonance spectrum.

  (C) From the viewpoint of satisfying the above physical properties of the low stereoregular olefin, the (C) low stereoregular olefin preferably contains a 1-butene polymer. The 1-butene polymer may be a 1-butene homopolymer, or at least one of 1-butene, ethylene, and an α-olefin having 3 to 20 carbon atoms (excluding 1-butene). Copolymers with olefins such as One type of 1-butene polymer may be used alone, or two or more types may be used in combination. The weight average molecular weight of the 1-butene polymer is preferably 10,000 or more. The mesopentad fraction (mmmm) of the 1-butene polymer is preferably 90% or less, more preferably 85% or less. Moreover, as melting | fusing point of 1-butene type polymer, Preferably it is 140 degrees C or less, More preferably, 100 degrees C or less is mentioned. In addition, as an upper limit of the weight average molecular weight of 1-butene type polymer, Preferably it is about 1 million, More preferably, about 500,000 is mentioned. The lower limit value of the mesopentad fraction (mmmm) is preferably 20%, more preferably 40%. The molecular weight distribution (Mw / Mn) of the 1-butene polymer is preferably 4 or less, more preferably 3.5 to 1.5, and still more preferably 3.0 to 1.5.

  (C) The low stereoregular olefin may be composed of only a 1-butene polymer, or may be a mixture of a 1-butene polymer and polyolefins. The polyolefin is not particularly limited as long as it can satisfy the above-described physical properties of the (C) low stereoregular olefin. For example, polyethylene, polypropylene, a poly α-olefin composed of α-olefin having 4 or more carbon atoms, polyvinylcyclo Examples include alkane, syndiocta polystyrene, polyalkenyl silane, and the like. Examples of polypropylene include homopolypropylene, which is a propylene-only polymer, such as propylene-ethylene random polypropylene, such as propylene / propylene-ethylene block polypropylene, and polyethylene includes high-density polyethylene, low-density polyethylene, such as ethylene. -Linear low density polyethylene such as butene-1, ethylene-hexene-1 and ethylene-octene-1. Examples of the poly α-olefin include polybutene-1, poly (4-methylpentene-1), poly (3-methylpentene-1), and poly (3-methylbutene-1). Preferred examples of the polyvinylcycloalkane include polyvinylcyclohexane and polyvinylcyclopentane. Examples of the polyalkenyl silane include those having an alkenyl group having 2 to 20 carbon atoms, such as vinyl silane, butene silane, and allyl silane. Among these, polypropylene, polyethylene and poly α-olefin are preferable from the viewpoint of compatibility, and polypropylene is more preferable from the viewpoint of heat resistance and flexibility. The weight average molecular weight of the polyolefin is preferably 10,000 or more. Polyolefins may be used alone or in combination of two or more.

  When the (C) low stereoregular olefin contains a 1-butene polymer and polyolefins, the mass ratio of the 1-butene polymer and polyolefins in the (C) low stereoregular olefin is not particularly limited. However, it is preferably about 1:99 to 99: 1, more preferably about 10:90 to 90:10, and still more preferably about 10:90 to 60:40.

  When the resin composition of the present invention contains (C) a low stereoregular olefin, the content of (C) the low stereoregular olefin is not particularly limited as long as the effect of the present invention is achieved, but preferably About 2-30 mass%, More preferably, it is about 3-25 mass%, More preferably, about 5-20 mass% is mentioned. When the resin composition of the present invention contains (C) a low stereoregular olefin, the content of the (B) polyolefin-based elastomer in the resin composition of the present invention is preferably about 20 to 65% by mass. More preferably, about 25-60 mass%, More preferably, about 20-50 mass% is mentioned.

  Although it does not restrict | limit especially as a melt flow rate (MFR) in 230 degreeC of the resin composition of this invention, Preferably it is 1-20 g / 10min, More preferably, 2.5-15g / 10min is mentioned. In the present invention, the melt flow rate is a value measured using a melt flow rate measuring device in accordance with the method described in JIS K7210.

  The resin composition of the present invention has the above-mentioned (A-1) random copolymer, (A-2) block copolymer, (B) polyolefin-based elastomer, as long as the effects of the present invention are not impaired. (C) A resin component other than the low stereoregular olefin may be included. As such a resin component, for example, in the above (A-1) random copolymer, (A-2) block copolymer, (B) polyolefin-based elastomer, and (C) low stereoregular olefin, Examples include those that do not satisfy at least one physical property, for example, (A-1) propylene-ethylene having a melting point of 156 ° C. or higher and an ethylene content exceeding 5% by mass as not satisfying the physical properties of the random copolymer. A random copolymer of propylene-ethylene having a melting point of less than 156 ° C. and an ethylene content of 5% by mass or less, and a propylene-ethylene random copolymer having a melting point of less than 156 ° C. and an ethylene content of more than 5% by mass Copolymers, etc .; (A-2) As those which do not satisfy the physical properties of block copolymers, the melting point is 158 ° C. or higher and the ethylene content is 7 % Block copolymer of propylene-ethylene, melting point of less than 158 ° C. and propylene-ethylene block copolymer of ethylene content of 7% by mass or less, melting point of less than 158 ° C. and ethylene content of 7% by mass Exceeding propylene-ethylene block copolymer, etc .; (B) Polyolefin elastomer having a melting point of less than 135 ° C. as not satisfying physical property value of polyolefin elastomer; (C) Satisfying physical property value of low stereoregular olefin No olefin having a weight average molecular weight of less than 10,000, a mesopentad fraction (mmmm) of 90% or less, a melting point of 70 ° C. or more, a weight average molecular weight of 10,000 or more, and a mesopentad fraction (mmmm) of 90%. An olefin having a melting point of 70 ° C. or higher, a weight average molecular weight of 10,000 or more, Olefin having a fraction (mmmm) of 90% or less, a melting point of less than 70 ° C, a weight average molecular weight of less than 10,000, a mesopentad fraction (mmmm) of more than 90%, and a melting point of 70 ° C or more, a weight average Olefin having a molecular weight of 10,000 or more, a mesopentad fraction (mmmm) of more than 90% and a melting point of less than 70 ° C., a weight average molecular weight of less than 10,000, a mesopentad fraction (mmmm) of 90% or less, and a melting point of 70 ° C. And olefins having a weight average molecular weight of less than 10,000, a mesopentad fraction (mmmm) of more than 90%, and a melting point of less than 70 ° C. The resin composition of the present invention contains a resin component other than (A-1) a random copolymer, (A-2) a block copolymer, (B) a polyolefin-based elastomer, and (C) a low stereoregular olefin. In this case, the total content of such resin components in the resin composition of the present invention is preferably 30% by mass or less, more preferably 25% by mass or less.

  The resin composition of this invention can be used conveniently as a resin composition which forms the sealant layer of the packaging material for batteries. Hereinafter, the battery packaging material produced using the resin composition of the present invention and the configuration of the battery will be described in detail.

2. Battery Packaging Material The battery packaging material is composed of a laminate having at least a base material layer 1, a metal layer 3, and a sealant layer 4 in this order. As shown in FIG. 1, the battery packaging material may have an adhesive layer 2 between the base material layer 1 and the metal layer 3. When the battery packaging material of the present invention is used in a battery, the base material layer 1 is the outermost layer and the sealant layer 4 is the innermost layer (battery element side). When assembling the battery, the sealant layers 4 located on the periphery of the battery element are brought into contact with each other and thermally welded to seal the battery element and seal the battery element. The battery packaging material may have an adhesive layer 5 between the metal layer 3 and the sealant layer 4 as shown in FIG.

3. Composition of each layer forming base material for battery [base material layer 1]
In the battery packaging material of the present invention, the base material layer 1 is a layer forming the outermost layer. The material for forming the base material layer 1 is not particularly limited as long as it has insulating properties. Examples of the material for forming the base material layer 1 include polyester, polyamide, epoxy, acrylic, fluororesin, polyurethane, silicon resin, phenol, polyetherimide, polyimide, and a mixture or copolymer thereof.

  Specific examples of the polyester include polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, polybutylene naphthalate, polyethylene isophthalate, polycarbonate, copolymerized polyester mainly composed of ethylene terephthalate, butylene terephthalate as a repeating unit. Examples thereof include a copolymer polyester mainly used. The copolymer polyester mainly composed of ethylene terephthalate is a copolymer polyester that polymerizes with ethylene isophthalate mainly composed of ethylene terephthalate (hereinafter, polyethylene (terephthalate / isophthalate)). Abbreviated), polyethylene (terephthalate / isophthalate), polyethylene (terephthalate / adipate), polyethylene (terephthalate / sodium sulfoisophthalate), polyethylene (terephthalate / sodium isophthalate), polyethylene (terephthalate / phenyl-dicarboxylate) And polyethylene (terephthalate / decanedicarboxylate). In addition, as a copolymer polyester mainly composed of butylene terephthalate as a repeating unit, specifically, a copolymer polyester that polymerizes with butylene isophthalate having butylene terephthalate as a repeating unit (hereinafter referred to as polybutylene (terephthalate / isophthalate)). For example), polybutylene (terephthalate / adipate), polybutylene (terephthalate / sebacate), polybutylene (terephthalate / decanedicarboxylate), polybutylene naphthalate and the like. These polyesters may be used individually by 1 type, and may be used in combination of 2 or more type. Polyester has the advantage of being excellent in electrolytic solution resistance and less likely to cause whitening due to the adhesion of the electrolytic solution, and is suitably used as a material for forming the base material layer 1.

  Specific examples of polyamides include aliphatic polyamides such as nylon 6, nylon 66, nylon 610, nylon 12, nylon 46, and copolymers of nylon 6 and nylon 6,6; terephthalic acid and / or Nylon 6I, Nylon 6T, Nylon 6IT, Nylon 6I6T (I represents isophthalic acid, T represents terephthalic acid) and the like, which include a structural unit derived from isophthalic acid, Aromatic polyamides such as silylene adipamide (MXD6); alicyclic polyamides such as polyaminomethylcyclohexyl adipamide (PACM6); and lactam components and isocyanate components such as 4,4′-diphenylmethane-diisocyanate. Polymerized polyamide, co-weight Polyester amide copolymer and polyether ester amide copolymer is a copolymer of polyamide and polyester and polyalkylene ether glycol; copolymers thereof, and the like. These polyamides may be used individually by 1 type, and may be used in combination of 2 or more type. The stretched polyamide film is excellent in stretchability, can prevent whitening due to resin cracking of the base material layer 1 during molding, and is suitably used as a material for forming the base material layer 1.

  The base material layer 1 may be formed of a uniaxially or biaxially stretched resin film, or may be formed of an unstretched resin film. Among them, a uniaxially or biaxially stretched resin film, in particular, a biaxially stretched resin film has improved heat resistance by orientation crystallization, and thus is suitably used as the base material layer 1. Moreover, the base material layer 1 may be formed by coating the above-mentioned raw material on the metal layer 3.

  Among these, as a resin film which forms the base material layer 1, Preferably nylon and polyester, More preferably, biaxially stretched nylon, biaxially stretched polyester, Most preferably, biaxially stretched nylon is mentioned.

  The base material layer 1 can also be laminated with at least one of resin films and coatings of different materials in order to improve pinhole resistance and insulation when used as a battery package. Specific examples include a multilayer structure in which a polyester film and a nylon film are laminated, and a multilayer structure in which a biaxially stretched polyester and a biaxially stretched nylon are laminated. When making the base material layer 1 into a multilayer structure, each resin film may be adhere | attached through an adhesive agent, and may be laminated | stacked directly without an adhesive agent. In the case of bonding without using an adhesive, for example, a method of bonding in a hot melt state such as a co-extrusion method, a sand lamination method, or a thermal laminating method can be mentioned. Moreover, when making it adhere | attach through an adhesive agent, the adhesive agent to be used may be a two-component curable adhesive, or a one-component curable adhesive. Further, the bonding mechanism of the adhesive is not particularly limited, and may be any of a chemical reaction type, a solvent volatilization type, a heat melting type, a hot pressure type, an electron beam curing type such as UV and EB, and the like. As an adhesive component, polyester resin, polyether resin, polyurethane resin, epoxy resin, phenol resin resin, polyamide resin, polyolefin resin, polyvinyl acetate resin, cellulose resin, (meth) acrylic resin Resins, polyimide resins, amino resins, rubbers, and silicon resins can be used.

  The base material layer 1 may be reduced in friction in order to improve moldability. In the case of reducing the friction of the base material layer 1, the friction coefficient of the surface is not particularly limited, but for example, 1.0 or less can be mentioned. In order to reduce the friction of the base material layer 1, for example, mat treatment, formation of a thin film layer of a slip agent, a combination thereof, and the like can be given.

  As the matting treatment, a matting agent is added to the base material layer 1 in advance to form irregularities on the surface, a transfer method by heating or pressurizing with an embossing roll, a surface is mechanically dry or wet blasting, or a file. There is a way to troll. Examples of the matting agent include fine particles having a particle size of about 0.5 nm to 5 μm. The material of the matting agent is not particularly limited, and examples thereof include metals, metal oxides, inorganic substances, and organic substances. The shape of the matting agent is not particularly limited, and examples thereof include a spherical shape, a fiber shape, a plate shape, an indeterminate shape, and a balloon shape. As a matting agent, specifically, talc, silica, graphite, kaolin, montmorilloid, montmorillonite, synthetic mica, hydrotalcite, silica gel, zeolite, aluminum hydroxide, magnesium hydroxide, zinc oxide, magnesium oxide, oxidation Aluminum, neodymium oxide, antimony oxide, titanium oxide, cerium oxide, calcium sulfate, barium sulfate, calcium carbonate, calcium silicate, lithium carbonate, calcium benzoate, calcium oxalate, magnesium stearate, alumina, carbon black, carbon nanotubes , High melting point nylon, crosslinked acrylic, crosslinked styrene, crosslinked polyethylene, benzoguanamine, gold, aluminum, copper, nickel and the like. These matting agents may be used individually by 1 type, and may be used in combination of 2 or more type. Among these matting agents, silica, barium sulfate, and titanium oxide are preferable from the viewpoint of dispersion stability and cost. The matting agent may be subjected to various surface treatments such as insulation treatment and high dispersibility treatment on the surface noodles.

  The thin film layer of the slip agent can be formed by depositing the slip agent on the surface of the base material layer 1 by bleeding out to form a thin layer, or by laminating the slip agent on the base material layer 1. The slip agent is not particularly limited. For example, fatty acid amide, metal soap, hydrophilic silicone, silicone grafted acrylic, silicone grafted epoxy, silicone grafted polyether, silicone grafted polyester, block silicone Examples thereof include acrylic copolymers, polyglycerol-modified silicone, and paraffin. These slip agents may be used individually by 1 type, and may be used in combination of 2 or more type.

  As for the thickness of the base material layer 1, 10-50 micrometers is mentioned, for example, Preferably 15-30 micrometers is mentioned.

[Adhesive layer 2]
In the battery packaging material of the present invention, the adhesive layer 2 is a layer provided as necessary in order to adhere the base material layer 1 and the metal layer 3.

  The adhesive layer 2 is formed of an adhesive capable of adhering the base material layer 1 and the metal layer 3. The adhesive used for forming the adhesive layer 2 may be a two-component curable adhesive or a one-component curable adhesive. Furthermore, the adhesive mechanism of the adhesive used for forming the adhesive layer 2 is not particularly limited, and may be any of a chemical reaction type, a solvent volatilization type, a heat melting type, a hot pressure type, and the like.

  Specific examples of the resin component of the adhesive that can be used to form the adhesive layer 2 include polyesters such as polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, polybutylene naphthalate, polyethylene isophthalate, polycarbonate, and copolyester. Resin; Polyether adhesive; Polyurethane adhesive; Epoxy resin; Phenol resin resin; Polyamide resin such as nylon 6, nylon 66, nylon 12, copolymer polyamide; polyolefin, acid-modified polyolefin, metal-modified polyolefin, etc. Polyolefin resin; polyvinyl acetate resin; cellulose adhesive; (meth) acrylic resin; polyimide resin; urea resin, melamine resin and other amino resins; chloroprene rubber, nitrile rubber, styrene - rubbers such as butadiene rubber, silicone resin; fluorinated ethylene propylene copolymer, and the like. These adhesive components may be used individually by 1 type, and may be used in combination of 2 or more type. The combination mode of two or more kinds of adhesive components is not particularly limited. For example, as the adhesive component, a mixed resin of polyamide and acid-modified polyolefin, a mixed resin of polyamide and metal-modified polyolefin, polyamide and polyester, Examples thereof include a mixed resin of polyester and acid-modified polyolefin, and a mixed resin of polyester and metal-modified polyolefin. Among these, extensibility, durability under high-humidity conditions, anti-hypertensive action, thermal deterioration-preventing action during heat sealing, etc. are excellent, and a decrease in lamination strength between the base material layer 1 and the metal layer 3 is suppressed. From the viewpoint of effectively suppressing the occurrence of delamination, a polyurethane two-component curable adhesive; polyamide, polyester, or a blended resin of these with a modified polyolefin is preferable.

  The adhesive layer 2 may be multilayered with different adhesive components. When the adhesive layer 2 is multilayered with different adhesive components, from the viewpoint of improving the lamination strength between the base material layer 1 and the metal layer 3, the adhesive component disposed on the base material layer 1 side is used as the base material layer 1. It is preferable to select a resin having excellent adhesion to the metal layer 3 and to select an adhesive component having excellent adhesion to the metal layer 3 as the adhesive component disposed on the metal layer 3 side. When the adhesive layer 2 is multilayered with different adhesive components, specifically, the adhesive component disposed on the metal layer 3 side is preferably an acid-modified polyolefin, a metal-modified polyolefin, a polyester and an acid-modified polyolefin. And a resin containing a copolyester.

  About the thickness of the contact bonding layer 2, 2-50 micrometers, for example, Preferably 3-25 micrometers is mentioned.

[Metal layer 3]
In the battery packaging material of the present invention, the metal layer 3 is a layer that functions as a barrier layer for preventing the penetration of water vapor, oxygen, light, etc. into the battery, in addition to improving the strength of the packaging material. Specific examples of the metal forming the metal layer 3 include metal foils such as aluminum, stainless steel, and titanium. Among these, aluminum is preferably used. In order to prevent wrinkles and pinholes during the production of the packaging material, soft aluminum such as annealed aluminum (JIS A8021P-O) or (JIS A8079P-O) is used as the metal layer 3 in the present invention. Is preferred.

  About thickness of the metal layer 3, 10-200 micrometers is preferable, for example, Preferably it is 20-100 micrometers.

  Further, the metal layer 3 is preferably subjected to chemical conversion treatment on at least one surface, preferably at least the surface on the sealant layer 4 side, and more preferably both surfaces, for the purpose of stabilizing adhesion, preventing dissolution and corrosion, and the like. . Here, the chemical conversion treatment is a treatment for forming an acid-resistant film on the surface of the metal layer 3. Chemical conversion treatment is, for example, chromate chromate treatment using a chromic acid compound such as chromium nitrate, chromium fluoride, chromium sulfate, chromium acetate, chromium oxalate, chromium biphosphate, chromic acetyl acetate, chromium chloride, potassium sulfate chromium, etc. ; Phosphoric acid chromate treatment using phosphoric acid compounds such as sodium phosphate, potassium phosphate, ammonium phosphate, polyphosphoric acid; aminated phenol heavy consisting of repeating units represented by the following general formulas (1) to (4) Examples thereof include chromate treatment using a coalescence.

In general formulas (1) to (4), X represents a hydrogen atom, a hydroxyl group, an alkyl group, a hydroxyalkyl group, an allyl group or a benzyl group. R ₁ and R ₂ are the same or different and represent a hydroxyl group, an alkyl group, or a hydroxyalkyl group. In the general formulas (1) to (4), examples of the alkyl group represented by X, R ₁ and R ₂ include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, C1-C4 linear or branched alkyl groups, such as a tert- butyl group, are mentioned. Examples of the hydroxyalkyl group represented by X, R ₁ and R ₂ include a hydroxymethyl group, a 1-hydroxyethyl group, a 2-hydroxyethyl group, a 1-hydroxypropyl group, a 2-hydroxypropyl group, 3- A linear or branched chain having 1 to 4 carbon atoms substituted with one hydroxy group such as hydroxypropyl group, 1-hydroxybutyl group, 2-hydroxybutyl group, 3-hydroxybutyl group, 4-hydroxybutyl group An alkyl group is mentioned. be able to. In the general formulas (1) to (4), X is preferably any one of a hydrogen atom, a hydroxyl group, and a droxyalkyl group. The number average molecular weight of the aminated phenol polymer composed of the repeating units represented by the general formulas (1) to (4) is, for example, about 500 to about 1,000,000, preferably about 1000 to about 20,000.

  In addition, as a chemical conversion treatment method for imparting corrosion resistance to the metal layer 3, a metal oxide such as aluminum oxide, titanium oxide, cerium oxide, tin oxide, or barium sulfate fine particles dispersed in phosphoric acid is coated. A method of forming a corrosion-resistant treatment layer on the surface of the metal layer 3 by performing a baking treatment at 150 ° C. or higher can be mentioned. Moreover, you may form the resin layer which crosslinked the cationic polymer with the crosslinking agent on the corrosion-resistant process layer. Here, as the cationic polymer, for example, polyethyleneimine, an ionic polymer complex composed of a polymer having polyethyleneimine and a carboxylic acid, a primary amine-grafted acrylic resin in which a primary amine is grafted on an acrylic main skeleton, polyallylamine, or Examples thereof include aminophenols and derivatives thereof. These cationic polymers may be used individually by 1 type, and may be used in combination of 2 or more type. Examples of the crosslinking agent include compounds having at least one functional group selected from the group consisting of isocyanate groups, glycidyl groups, carboxyl groups, and oxazoline groups, silane coupling agents, and the like. These crosslinking agents may be used alone or in combination of two or more.

  These chemical conversion treatments may be performed alone or in combination of two or more chemical conversion treatments. Furthermore, these chemical conversion treatments may be carried out using one kind of compound alone, or may be carried out using a combination of two or more kinds of compounds. Among these, chromic acid chromate treatment is preferable, and chromate treatment in which a chromic acid compound, a phosphoric acid compound, and an aminated phenol polymer are combined is more preferable.

The amount of the acid-resistant film formed on the surface of the metal layer 3 in the chemical conversion treatment is not particularly limited. For example, if the chromate treatment is performed by combining a chromic acid compound, a phosphoric acid compound, and an aminated phenol polymer. The chromic acid compound is about 0.5 to about 50 mg, preferably about 1.0 to about 40 mg in terms of chromium, and the phosphorus compound is about 0.5 to about 50 mg in terms of phosphorus per 1 m ² of the surface of the metal layer 3. Is preferably about 1.0 to about 40 mg, and about 1 to about 200 mg, preferably about 5.0 to 150 mg of aminated phenol polymer.

  In the chemical conversion treatment, a solution containing a compound used for forming an acid-resistant film is applied to the surface of the metal layer 3 by a bar coating method, a roll coating method, a gravure coating method, a dipping method or the like, and then the temperature of the metal layer 3 is reached. Is performed by heating so as to be about 70 to 200 ° C. In addition, before the chemical conversion treatment is performed on the metal layer 3, the metal layer 3 may be subjected to a degreasing treatment by an alkali dipping method, an electrolytic cleaning method, an acid cleaning method, an electrolytic acid cleaning method, or the like in advance. By performing the degreasing treatment in this way, it becomes possible to more efficiently perform the chemical conversion treatment on the surface of the metal layer 3.

[Sealant layer 4]
In the battery packaging material of the present invention, the sealant layer 4 corresponds to the innermost layer, and the sealant layers 4 are heat-welded to each other to seal the battery element when the battery is assembled. The sealant layer 4 may be composed of one layer formed of the resin composition of the present invention, or may be composed of a plurality of layers formed of the resin composition. The sealant layer 4 may further include one or more other layers in addition to the layer formed of the resin composition of the present invention. The resin forming the other layer is not particularly limited as long as the effects of the present invention are exhibited, and examples thereof include polyolefin, cyclic polyolefin, carboxylic acid-modified polyolefin, and carboxylic acid-modified cyclic polyolefin.

  Specific examples of polyolefins include polyethylene such as low density polyethylene, medium density polyethylene, high density polyethylene, and linear low density polyethylene; homopolypropylene, polypropylene block copolymers (for example, block copolymers of propylene and ethylene), polypropylene Crystalline or amorphous polypropylene such as random copolymers (eg, random copolymers of propylene and ethylene); ethylene-butene-propylene terpolymers, and the like. Among these polyolefins, polyethylene and polypropylene are preferable.

  Cyclic polyolefin is a copolymer of olefin and cyclic monomer. Examples of the olefin include ethylene, propylene, 4-methyl-1-pentene, styrene, butadiene, and isoprene. Examples of the cyclic monomer include cyclic alkenes such as norbornene; cyclic dienes such as cyclopentadiene, dicyclopentadiene, cyclohexadiene, norbornadiene, and the like. Among these polyolefins, a cyclic alkene is preferable, and norbornene is more preferable.

  A carboxylic acid-modified polyolefin is a polymer obtained by modifying a polyolefin with a carboxylic acid. Examples of the carboxylic acid used for modification include maleic acid, acrylic acid, itaconic acid, crotonic acid, maleic anhydride, itaconic anhydride and the like.

  The carboxylic acid-modified cyclic polyolefin is a copolymer obtained by copolymerizing a part of the monomer constituting the cyclic polyolefin in place of the α, β-unsaturated carboxylic acid or its acid anhydride, or α, β with respect to the cyclic polyolefin. -A polymer obtained by block copolymerization or graft copolymerization of an unsaturated carboxylic acid or its acid anhydride. The cyclic polyolefin to be modified with carboxylic acid can be the same as the above cyclic polyolefin. The carboxylic acid used for modification can be the same as that used for modification of the acid-modified cycloolefin copolymer.

  Among these resin components, preferably crystalline or amorphous polyolefin, cyclic polyolefin, and blended polymers thereof; more preferably polyethylene, polypropylene, copolymers of ethylene and norbornene, and two or more of these The blend polymer of these is mentioned.

  The other layer may be formed from only one type of resin component, or may be formed from a blend polymer that combines two or more types of resin components.

  The thickness of the sealant layer 4 is not particularly limited, but can be, for example, about 2 μm to 2000 μm, preferably about 5 μm to 1000 μm, and more preferably 10 μm to 500 μm.

[Adhesive layer 5]
In the battery packaging material of the present invention, an adhesive layer is provided between the metal layer 3 and the sealant layer 4 for the purpose of firmly bonding the metal layer 3 and the sealant layer 4 as shown in FIG. 5 may be further provided. The adhesive layer 5 may be formed of one layer or may be formed of a plurality of layers.

  The adhesive layer 5 is formed of a resin capable of bonding the metal layer 3 and the sealant layer 4. The resin forming the adhesive layer 5 is not particularly limited as long as it is a resin capable of adhering the metal layer 3 and the sealant layer 4, but preferably the acid-modified polyolefin, polyester resin, fluorine resin, or polyether resin described above. , Polyurethane resin, epoxy resin, phenol resin resin, polyamide resin, polyolefin resin, polyvinyl acetate resin, cellulose resin, (meth) acrylic resin, polyimide resin, amino resin, rubber, silicon Examples thereof include resins. The resin forming the adhesive layer 5 may be used alone or in combination of two or more.

  The acid-modified polyolefin is a polymer modified by graft polymerization of polyolefin with an unsaturated carboxylic acid. Specific examples of the acid-modified polyolefin include polyethylene such as low density polyethylene, medium density polyethylene, high density polyethylene, and linear low density polyethylene; homopolypropylene, block copolymer of polypropylene (for example, block copolymer of propylene and ethylene) ), A random or amorphous polypropylene copolymer (for example, a random copolymer of propylene and ethylene), and a terpolymer of ethylene-butene-propylene. Among these polyolefins, from the viewpoint of heat resistance, polyolefins having at least propylene as a constituent monomer are preferable, and ethylene-butene-propylene terpolymers and propylene-ethylene random copolymers are more preferable. Examples of the unsaturated carboxylic acid used for modification include maleic acid, acrylic acid, itaconic acid, crotonic acid, maleic anhydride, itaconic anhydride and the like. Among these unsaturated carboxylic acids, maleic acid and maleic anhydride are preferable. These acid-modified polyolefins may be used individually by 1 type, and may be used in combination of 2 or more type.

  Polyester resins include polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, polybutylene naphthalate, polyethylene isophthalate, polycarbonate, copolymer polyester mainly composed of ethylene terephthalate, and copolymer mainly composed of butylene terephthalate. Examples include polymerized polyester. The copolymer polyester mainly composed of ethylene terephthalate is a copolymer polyester that polymerizes with ethylene isophthalate mainly composed of ethylene terephthalate (hereinafter, polyethylene (terephthalate / isophthalate)). Abbreviated), polyethylene (terephthalate / isophthalate), polyethylene (terephthalate / adipate), polyethylene (terephthalate / sodium sulfoisophthalate), polyethylene (terephthalate / sodium isophthalate), polyethylene (terephthalate / phenyl-dicarboxylate) And polyethylene (terephthalate / decanedicarboxylate). In addition, as a copolymer polyester mainly composed of butylene terephthalate as a repeating unit, specifically, a copolymer polyester that polymerizes with butylene isophthalate having butylene terephthalate as a repeating unit (hereinafter referred to as polybutylene (terephthalate / isophthalate)). For example), polybutylene (terephthalate / adipate), polybutylene (terephthalate / sebacate), polybutylene (terephthalate / decanedicarboxylate), polybutylene naphthalate and the like. These polyester resins may be used individually by 1 type, and may be used in combination of 2 or more type.

  Fluorocarbon resins include tetrafluoroethylene, trifluoroethylene, polyvinylidene fluoride, polyvinyl fluoride, ethylene tetrafluoroethylene, polychlorotrifluoroethylene, ethylene chlorotrifluoroethylene copolymer, tetrafluoroethylene-hexafluoropropylene copolymer A polymer, a fluorine-type polyol, etc. are mentioned. These fluororesins may be used alone or in combination of two or more.

  The adhesive layer 5 may be formed of at least one of these resins, and may contain other resin components as necessary. When the adhesive layer 5 contains other resin components, the acid-modified polyolefin, polyester resin, fluororesin, polyether resin, polyurethane resin, epoxy resin, phenol resin resin, polyamide resin in the sealant layer 4 Resin, polyolefin resin, polyvinyl acetate resin, cellulose resin, (meth) acrylic resin, polyimide resin, amino resin, rubber, and silicon resin content, as long as the effects of the present invention are not hindered Although it does not restrict | limit in particular, For example, 10-95 mass%, Preferably it is 30-90 mass%, Furthermore, 50-80 mass% is mentioned.

  Moreover, it is preferable that the contact bonding layer 5 further contains a hardening | curing agent. When the adhesive layer 5 contains a curing agent, the mechanical strength of the adhesive layer 5 can be increased, and the insulation of the battery packaging material can be effectively increased. A hardening | curing agent may be used individually by 1 type, and may be used in combination of 2 or more types.

  Curing agents are acid-modified polyolefin, polyester resin, fluorine resin, polyether resin, polyurethane resin, epoxy resin, phenol resin resin, polyamide resin, polyolefin resin, polyvinyl acetate resin, cellulose resin , (Meth) acrylic resin, polyimide resin, amino resin, rubber, or silicon resin is not particularly limited. As a hardening | curing agent, a polyfunctional isocyanate compound, a carbodiimide compound, an epoxy compound, an oxazoline compound etc. are mentioned, for example.

  The polyfunctional isocyanate compound is not particularly limited as long as it is a compound having two or more isocyanate groups. Specific examples of the polyfunctional isocyanate compound include isophorone diisocyanate (IPDI), hexamethylene diisocyanate (HDI), tolylene diisocyanate (TDI), diphenylmethane diisocyanate (MDI), those obtained by polymerizing or nurate, mixtures thereof, Examples include copolymers with other polymers.

  The carbodiimide compound is not particularly limited as long as it is a compound having at least one carbodiimide group (—N═C═N—). As the carbodiimide compound, a polycarbodiimide compound having at least two carbodiimide groups is preferable. Specific examples of particularly preferred carbodiimide compounds include the following general formula (5):

[In General formula (5), n is an integer greater than or equal to 2. ]
A polycarbodiimide compound having a repeating unit represented by:
The following general formula (6):

[In General formula (6), n is an integer greater than or equal to 2. ]
A polycarbodiimide compound having a repeating unit represented by:
And the following general formula (7):

[In General formula (7), n is an integer greater than or equal to 2. ]
The polycarbodiimide compound represented by these is mentioned. In general formula (4)-(7), n is an integer of 30 or less normally, Preferably it is an integer of 3-20.

  The epoxy compound is not particularly limited as long as it is a compound having at least one epoxy group. Examples of the epoxy compound include epoxy resins such as bisphenol A diglycidyl ether, modified bisphenol A diglycidyl ether, novolac glycidyl ether, glycerin polyglycidyl ether, and polyglycerin polyglycidyl ether.

  The oxazoline compound is not particularly limited as long as it is a compound having an oxazoline skeleton. Specific examples of the oxazoline compound include Epocross series manufactured by Nippon Shokubai Co., Ltd.

  From the standpoint of increasing the mechanical strength of the adhesive layer 5, the curing agent may be composed of two or more types of compounds.

  In the adhesive layer 5, the content of the curing agent is acid-modified polyolefin, polyester resin, fluorine resin, polyether resin, polyurethane resin, epoxy resin, phenol resin resin, polyamide resin, polyolefin resin, poly It should be in the range of 0.1 to 50 parts by weight with respect to 100 parts by weight of vinyl acetate resin, cellulose resin, (meth) acrylic resin, polyimide resin, amino resin, rubber, or silicon resin. It is more preferable that it is in the range of 0.1 to 30 parts by mass. Further, in the adhesive layer 5, the content of the curing agent is preferably in the range of 1 equivalent to 30 equivalents as a reactive group in the curing agent with respect to 1 equivalent of the carboxyl group in each resin such as acid-modified polyolefin. More preferably, it is in the range of 1 equivalent to 20 equivalents. Thereby, the insulation and durability of the battery packaging material can be further improved.

  When the adhesive layer 5 includes a curing agent, the adhesive layer 5 may be formed of a two-component curable adhesive resin or a one-component curable adhesive resin. Further, the bonding mechanism of the adhesive is not particularly limited, and may be any of a chemical reaction type, a solvent volatilization type, a heat melting type, a hot pressure type, an electron beam curing type such as UV and EB, and the like.

  Although it does not restrict | limit especially as thickness of the contact bonding layer 5, Preferably it is 0.01 micrometer or more, More preferably, 0.05-20 micrometers is mentioned. If the thickness of the adhesive layer 5 is less than 0.01 μm, it may be difficult to stably bond the metal layer 3 and the sealant layer 4.

4). Method for Producing Battery Packaging Material The method for producing the battery packaging material of the present invention is not particularly limited as long as a laminate in which layers having a predetermined composition are laminated is obtained. For example, the following method is exemplified. .

  First, a laminate in which the base material layer 1, the adhesive layer 2, and the metal layer 3 are laminated in order (hereinafter also referred to as “laminate A”) is formed. Specifically, the laminate A is formed by using a thermal laminating method, a sand laminating method, using an adhesive that forms the adhesive layer 2 on the base material 1 and the metal layer 3 whose surface is subjected to a chemical conversion treatment if necessary. It is performed by laminating by a method or a combination thereof.

  The laminate A is formed by the thermal laminating method. For example, a multilayer film in which the base material layer 1 and the adhesive layer 2 are laminated is prepared in advance, and the metal layer 3 is superimposed on the adhesive layer 2 and heated with a heating roll. It can be performed by thermocompression bonding with the adhesive layer 2 sandwiched between the layer 1 and the metal layer 3. The laminate A is formed by the thermal laminating method in which a multilayer film in which the metal layer 3 and the adhesive layer 2 are laminated is prepared in advance, and the base material layer 1 is superposed on the heated metal layer 3 and the adhesive layer 2. It may be performed by thermocompression bonding while sandwiching the adhesive layer 2 between the base material layer 1 and the metal layer 3. In addition, the base material layer 1 and the metal layer 3 may be directly laminated without using the adhesive layer 2.

  In addition, the multilayer film in which the base material layer 1 and the adhesive layer 2 prepared in advance in the thermal laminating method are laminated on the resin film constituting the base material layer 1 by melt extrusion or solution coating of the adhesive constituting the adhesive layer 2. After being laminated and dried by (liquid coating), the adhesive layer 2 is formed by baking at a temperature equal to or higher than the melting point of the adhesive. By performing baking, the adhesive strength between the metal layer 3 and the adhesive layer 2 is improved. Similarly, for a multilayer film in which the metal layer 3 and the adhesive layer 2 prepared in advance in the thermal laminating method are laminated, the adhesive constituting the adhesive layer 2 is melt-extruded or solution into the metal foil constituting the metal layer 3 in the same manner. After being laminated by coating and dried, it is formed by baking at a temperature equal to or higher than the melting point of the adhesive constituting the adhesive layer 2.

  The laminate A is formed by the sand lamination method, for example, by melting and extruding the adhesive constituting the adhesive layer 2 onto the upper surface of the metal layer 3 and bonding the resin film constituting the base material layer 1 to the metal layer. Can be performed. At this time, it is desirable that the resin film is bonded and temporarily bonded, and then heated again to perform the main bonding. In the sand lamination method, the adhesive layer 2 may be multilayered with different resin types. In this case, a multilayer film in which the base material layer 1 and the adhesive layer 2 are laminated is prepared in advance, the adhesive constituting the adhesive layer 2 is melt-extruded on the upper surface of the metal layer 3, and the multilayer resin film and the thermal lamination method are used. What is necessary is just to laminate. Thereby, the adhesive layer 2 which comprises a multilayer film, and the adhesive layer 2 laminated | stacked on the upper surface of the metal layer 3 adhere | attach, and the two-layer adhesive layer 2 is formed. When the adhesive layer 2 is multilayered with different resin types, a multilayer film in which the metal layer 3 and the adhesive layer 2 are laminated is prepared in advance, and the adhesive constituting the adhesive layer 2 is melted on the base material layer 1 It may be extruded and laminated with the adhesive layer 2 on the metal layer 3. Thereby, the adhesive layer 2 composed of two different adhesives is formed between the multilayer resin film and the base material layer 1.

  Next, the sealant layer 4 is laminated on the metal layer 3 of the laminate A. Lamination of the sealant layer 4 on the metal layer 3 of the laminate A can be performed by a coextrusion method, a thermal lamination method, a sand lamination method, a coating method, or a combination thereof. For example, when the adhesive layer 5 is not provided, the sealant layer 4 can be formed on the metal layer 3 by melt extrusion, thermal lamination, coating, or the like. When the adhesive layer 5 is provided, the sealant layer 4 can be formed by the same method after the adhesive layer 5 is formed on the metal layer 3 by a melt extrusion method, a thermal laminating method, a coating method, or the like. Further, a co-extrusion method in which the adhesive layer 5 and the sealant layer 4 are simultaneously melt-extruded on the metal layer 3 may be performed. Moreover, while the adhesive layer 5 is melt-extruded on the metal layer 3, a sand laminating method in which the film-like sealant layer 4 is bonded can also be performed. When the sealant layer 4 is formed of two layers, for example, one layer of the adhesive layer 5 and the sealant layer 4 is coextruded on the metal layer 3, and then another layer of the sealant layer 4 is pasted by a thermal lamination method. The method of attaching is mentioned. Further, there may be mentioned a method in which one layer of the adhesive layer 5 and the sealant layer 4 is coextruded on the metal layer 3 and another layer of the film-like sealant layer 4 is bonded. In addition, when making the sealant layer 4 into three or more layers, the sealant layer 4 can be further formed by a melt extrusion method, a thermal lamination method, a coating method, or the like.

  As described above, it comprises: base material layer 1 / adhesive layer 2 provided as needed / metal layer 3 whose surface is subjected to chemical conversion treatment as needed / adhesive layer 5 / sealant layer 4 provided as needed A laminate is formed. In order to strengthen the adhesiveness of the adhesive layer 2, it may be further subjected to heat treatment such as hot roll contact, hot air, near or far infrared irradiation, dielectric heating, heat resistance heating and the like. Examples of such heat treatment conditions include 150 to 250 ° C. and 1 to 10 hours.

  Moreover, in the battery packaging material of the present invention, each layer constituting the laminate improves or stabilizes film forming properties, lamination processing, suitability for final processing (pouching, embossing), etc., as necessary. Therefore, surface activation treatment such as corona treatment, blast treatment, oxidation treatment, and ozone treatment may be performed.

5. Application of Battery Packaging Material The battery packaging material of the present invention is used as a packaging material for sealing and housing battery elements such as a positive electrode, a negative electrode, and an electrolyte.

  Specifically, a battery element including at least a positive electrode, a negative electrode, and an electrolyte is formed with a flange (sealant layer) on the periphery of the battery element in a state in which a metal terminal connected to each of the positive electrode and the negative electrode protrudes outward. The area | region which mutually contacts) can be formed, and it coat | covers with the battery packaging material of this invention. Next, the battery sealed with the battery packaging material of the present invention is provided by heat-sealing and sealing the sealant layers of the flange part. When the battery element is accommodated using the battery packaging material of the present invention, the battery packaging material of the present invention is used so that the sealant layer 4 is on the inner side (surface in contact with the battery element).

  The battery packaging material of the present invention can be used for both primary batteries and secondary batteries, but is particularly suitable for use in secondary batteries. The type of the secondary battery to which the battery packaging material of the present invention is applied is not particularly limited. Nickel / iron livestock batteries, nickel / zinc livestock batteries, silver oxide / zinc livestock batteries, metal-air batteries, multivalent cation batteries, capacitors, capacitors, and the like. Among these secondary batteries, lithium ion batteries and lithium ion polymer batteries are suitable applications for the battery packaging material of the present invention.

  In the battery packaging material of the present invention, the seal strength of the part heat-sealed with the sealant layers 4 facing each other (heat-sealing conditions: 190 ° C., 3 seconds at a surface pressure of 1.0 MPa) at 25 ° C. Preferably 30 (N / 15mm) or more, More preferably, 40-200 (N / 15mm) is mentioned. In addition, in the battery packaging material of the present invention, the seal strength of the part heat-sealed with the sealant layers 4 facing each other (heat-sealing conditions: 190 ° C., 3 seconds at a surface pressure of 1.0 MPa) is 125 ° C. In the above, preferably 4 (N / 15 mm) or more, more preferably 5 to 100 (N / 15 mm). Further, the tensile yield point strength (MD + TD) of the battery packaging material of the present invention is preferably 50 MPa or less, more preferably 35 MPa or less. When the tensile yield point strength of the battery packaging material of the present invention is such a low value, the sealant layer 4 is soft, and the occurrence of cracks when the battery packaging material is stretched is more effectively suppressed. In addition, the moldability is excellent, and furthermore, since the generation of cracks when the seal portion is bent is more effectively suppressed, the insulation is also excellent. That is, high flexibility can be imparted to the resin composition without substantially lowering the melting point of the resin composition. As a result, when the resin composition of the present invention is used for the sealant layer of the battery packaging material, the tensile yield point strength (MD + TD) of the battery packaging material described later can be lowered. The effect of making the pressure uniform becomes high, uniform sealing becomes possible, and high sealing performance is obtained. In addition, in resin cooling that occurs after heat sealing, the effect of suppressing the growth of crystal nuclei and the increase in the number of crystal nuclei in the resin composition is manifested, and fine cracks that occur due to increase in crystal nuclei after sealing and non-uniformization, etc. Can be prevented. For this reason, while being able to raise seal strength, it also becomes possible to suppress the permeability of the electrolyte solution which is the contents, and the stable sealing nature is obtained. The tensile yield point strength of the battery packaging material of the present invention is a value measured by a method based on JIS K7161-1994.

  Hereinafter, the present invention will be described in detail with reference to Examples and Comparative Examples. However, the present invention is not limited to the examples.

Example 1-10 and Comparative Example 1-6
[Manufacture of battery packaging materials]
On a base material layer made of a biaxially stretched nylon film (thickness 25 μm), a metal layer made of an aluminum foil (thickness 40 μm) subjected to chemical conversion treatment on both surfaces was laminated by a dry lamination method. Specifically, a two-component urethane adhesive (a polyester-based main agent and an isocyanate-based curing agent) was applied to one surface of the aluminum foil, and an adhesive layer (thickness 4 μm) was formed on the metal layer. Next, after the adhesive layer and the base material layer on the metal layer were pressure-heat bonded, a laminate of base material layer / adhesive layer / metal layer was prepared by performing an aging treatment at 60 ° C. for 24 hours. . In addition, the chemical conversion treatment of the aluminum foil used as the metal layer is performed by roll coating a treatment liquid composed of a phenol resin, a chromium fluoride compound, and phosphoric acid so that the coating amount of chromium is 10 mg / m ² (dry weight). The coating was performed on both surfaces of the aluminum foil by the method and baked for 20 seconds under the condition that the film temperature was 180 ° C. or higher.

Next, an adhesive layer formed of a carboxylic acid-modified polypropylene resin and a sealant layer 4 formed of a resin listed in Table 1 were laminated on the metal layer by a coextrusion method. Thus, a battery packaging material comprising a laminate in which the base layer / adhesive layer / metal layer / adhesive layer / sealant layer was laminated in order was obtained. The resin used for the sealant layer 4 is a propylene-ethylene copolymer, a propylene-based elastomer, and a low stereoregular resin described in Table 1. The product names of the low stereoregular resins used in Examples and Comparative Examples are as follows.
<Low stereoregular olefin>
Examples 3, 5, 10 and Comparative Example 6: Product name “El Modu S400” manufactured by Idemitsu Kosan Co., Ltd.
Example 4: Product name “El Modu S901” manufactured by Idemitsu Kosan Co., Ltd.

The melting point of each resin component is a value measured by a differential scanning calorimeter (DSC). Further, the melt flow rate (MFR) at 230 ° C. is a value measured using a melt flow rate measuring device in accordance with the method described in JIS K7210. The weight average molecular weight is a value measured by gel permeation chromatography (GPC) using polystyrene as a standard sample. The mesopentad fraction (mmmm) of the low stereoregular olefin is a value measured by measuring a ¹³ C nuclear magnetic resonance spectrum.

  Next, the following items were evaluated for the battery packaging materials obtained in Examples 1 to 10 and Comparative Examples 1 to 6, respectively. The results are shown in Table 2.

<Measurement of tensile yield strength>
The tensile yield strength was measured according to JIS K7161-1994, by preparing a sample having a width of 15 mm and a length of 100 mm, and a tensile speed of 300 mm / min.

<Measurement of seal strength>
(1) In the case of 25 ° C. The battery packaging materials are stacked so that the sealant layers face each other, heat sealed under conditions of 190 ° C. and a surface pressure of 1.0 MPa for 3 seconds, and then left at 25 ° C. for 2 minutes. Under 25 ° C., the sealant layer of the heat seal part was peeled 10 mm at a rate of 300 mm / min with a tensile tester (manufactured by Shimadzu Corporation, AGS-50D (trade name)), and the maximum strength at the time of peeling was defined as the seal strength.
(2) In the case of 125 ° C. The battery packaging materials are stacked so that the sealant layers face each other, heat sealed under conditions of 190 ° C. and a surface pressure of 1.0 MPa for 3 seconds, and then left at 125 ° C. for 2 minutes. Under 125 ° C., the sealant layer of the heat seal part was peeled 10 mm at a speed of 300 mm / min with a tensile tester (manufactured by Shimadzu Corporation, AGS-50D (trade name)), and the maximum strength at the time of peeling was defined as the seal strength.
(3) When exposed to electrolyte solution The battery packaging material was cut into 150 mm (MD direction, vertical direction) × 80 mm (TD direction, horizontal direction), respectively, and then folded at the center in the MD direction to be 75 mm × 80 mm. . Next, the two sides in the MD direction were heat-sealed so as to have a width of 7 mm and an inner dimension of 75 mm (MD direction) × 65 mm (TD direction) to form a bag. Next, 3 g of electrolyte solution (consisting of 1M LiPF ₆ and a mixed solution of ethylene carbonate, diethyl carbonate and dimethyl carbonate (capacity ratio 1: 1: 1)) is filled from the opening on one side which is not heat sealed. This one side was heat sealed. The heat seal conditions were 190 ° C. and a surface pressure of 1.0 MPa for 3 seconds. Next, the ring was left to stand at 65 ° C. for 14 days, with the last heat-sealed side facing down. Next, after standing at room temperature until reaching 25 ° C., the sealant layer of the heat seal part is 10 mm at a speed of 300 mm / min with a tensile tester (manufactured by Shimadzu Corp., AGS-50D (trade name)) at 25 ° C. The maximum strength at the time of peeling was defined as the seal strength.

<Presence or absence of cracks due to stretching>
After cutting each battery packaging material into 150 mm (MD direction) × 80 mm (TD direction), with a molding die (female die) having a caliber of 35 mm × 50 mm and a corresponding molding die (male die), Cold forming was performed at a depth of 3.0 mm at 0.4 MPa, and a recess was formed at the center. Then, the presence or absence of the whitening of a recessed part was confirmed visually.

<Evaluation of insulation after bending the seal part>
The battery packaging material was cut into 60 mm (MD direction) × 60 mm (TD direction) sheet pieces. Next, these sheet pieces were folded in the MD direction, and two opposing sides were heat-sealed with a width of 7 mm to prepare a pouch-type exterior body having an opening on one side. Next, the obtained exterior body is sealed with a lithium ion battery main body including cells so that the metal terminal extends to the outside from one side of the opening, and the opening is formed while holding the metal terminal with the electrolytic solution. A lithium ion battery was produced by hermetically sealing with a width of 3 mm. At this time, the heat sealing was performed under the conditions of a surface pressure of 2.0 MPa, a sealing temperature of 170 ° C., and a sealing time of 5.0 seconds. Next, the heat-sealed portion of the obtained lithium ion battery was bent inward and returned to its original state. Next, the insulation evaluation test with respect to a crack was implemented using the impulse application system (Nippon Technate make, a lithium ion battery insulation tester). First, prepare 10 lithium ion batteries, apply an impulse voltage of 100 V applied between the negative electrode terminal of each lithium ion battery and the aluminum foil, and have a voltage drop within 40 V after 99 msec. The product was accepted, and the product with an acceptable product ratio of 50% or more was evaluated as ◯. An acceptable product with a ratio of less than 50% was evaluated as x.

  As shown in Tables 1 and 2, a propylene-ethylene random copolymer having a melting point of 156 ° C. or higher and an ethylene content of 5% by mass or less and a polypropylene elastomer having a melting point of 135 ° C. or higher are used for the sealant layer. In the battery packaging materials of Examples 1 and 2, the tensile yield point strength was low, and the seal strength was high at 25 ° C., 125 ° C., and when exposed to the electrolyte. Furthermore, in the battery packaging materials of Examples 1 and 2, no cracks due to stretching were observed, and the insulation after bending the seal portion was high. Moreover, in the battery packaging materials of Examples 3 to 5 in which the low stereoregular olefin was further blended in the sealant layer, the tensile yield point strength was further reduced and the seal strength was also extremely high.

  Battery packaging materials of Examples 6 to 9 using a propylene-ethylene block copolymer having a melting point of 158 ° C. or higher and an ethylene content of 7% by mass or less and a polypropylene elastomer having a melting point of 135 ° C. or higher for the sealant layer. Also, the tensile yield point strength was low, and the seal strength was high at 25 ° C., 125 ° C., and when exposed to the electrolyte. Furthermore, in the battery packaging materials of Examples 6 to 9, no cracks due to stretching were observed, and the insulation after bending the seal portion was high. In addition, in the battery packaging material of Example 10 in which the low stereoregular olefin was further blended in the sealant layer, the tensile yield point strength was further reduced and the seal strength was also very high.

  On the other hand, in the battery packaging material of Comparative Example 1 in which the sealant layer was formed of polyethylene, the tensile yield point strength was low, but the seal strength at 125 ° C. tended to be low, and the seal strength after being exposed to the electrolyte solution Was significantly lower. Comparative Example 2 where a propylene-ethylene random copolymer having a melting point of 156 ° C. or higher and an ethylene content of 5% by mass or less was used for the sealant layer, but a polypropylene elastomer having a melting point of 135 ° C. or higher was not used. In the battery packaging materials of No. 3 and No. 3, the insulation after bending the seal portion was low. Further, the battery packaging materials of Comparative Examples 2 and 3 showed a tendency that the sealing strength at 125 ° C. was lowered, and cracks in stretching were also observed. The battery packaging material of Comparative Example 5 in which a propylene-ethylene random copolymer having a melting point of 156 ° C. or higher and an ethylene content of 5% by mass or less was used for the sealant layer, but a polypropylene elastomer having a melting point of 80 ° C. Then, the sealing strength after exposure to the electrolytic solution was low, discoloration of the electrolytic solution was observed, and dissolution of the added polypropylene elastomer was observed. Moreover, in the comparative example 5, the crack by extending | stretching was also recognized and the insulation after bending a seal part was bad.

  In the battery packaging material of Comparative Example 4 in which a propylene-ethylene block copolymer having a melting point of 158 ° C. or more and an ethylene content of 7% by mass or less was used, but a polypropylene elastomer having a melting point of 135 ° C. or more was not used. In addition, the tensile yield point strength was very high, and cracks were observed during stretching. Although a polypropylene elastomer having a melting point of 135 ° C. or more and a low stereoregular olefin having a meso pendant fraction (mmmm) of 90% or less, a random copolymer of propylene-ethylene having a melting point of 132 ° C. and an ethylene content of 8% by mass. In Comparative Example 6 using the polymer, the tensile yield point strength was low, but the seal strength at 125 ° C. was low.

1 Base material layer 2 Adhesive layer 3 Metal layer 4 Sealant layer 5 Adhesive layer

Claims (8)

(A-1) a random copolymer of propylene-ethylene having a melting point of 156 ° C. or higher and an ethylene content of 5% by mass or less, and (A-2) a melting point of 158 ° C. or higher and an ethylene content of 7% by mass or less. At least one of a propylene-ethylene block copolymer;
(B) a polyolefin-based elastomer having a melting point of 135 ° C. or higher;
A resin composition for a sealant layer of a battery packaging material.   2. The resin composition according to claim 1, wherein the content of the (B) melting point of the polyolefin-based elastomer having a melting point of 135 ° C. or higher is 20 to 75% by mass.   (A-1) a random copolymer of propylene-ethylene having a melting point of 156 ° C. or higher and an ethylene content of 5% by mass or less, and (A-2) a melting point of 158 ° C. or higher and an ethylene content of 7% by mass or less. The resin composition according to claim 1 or 2, wherein the total content of the block copolymer of propylene-ethylene is 25 to 80% by mass.   The resin according to any one of claims 1 to 3, further comprising (C) a low stereoregular olefin having a weight average molecular weight of 10,000 or more, a mesopentad fraction (mmmm) of 90% or less, and a melting point of 70 ° C or more. Composition.   The resin composition according to any one of claims 1 to 4, wherein the (C) low stereoregular olefin contains a 1-butene polymer.   The content of the (B) polyolefin elastomer having a melting point of 135 ° C. or more is 20 to 65% by mass, the (C) weight average molecular weight is 10,000 or more, the mesopentad fraction (mmmm) is 90% or less, and the melting point is 70. The resin composition according to any one of claims 1 to 5, wherein the content of the low stereoregular olefin that is at least ° C is 2 to 30% by mass. A battery packaging material comprising a laminate having at least a base material layer, a metal layer, and a sealant layer in this order,
The battery packaging material in which the said sealant layer contains the layer formed with the resin composition in any one of Claims 1-6.   A battery in which a battery element including a positive electrode, a negative electrode, and an electrolyte is sealed with the battery packaging material according to claim 7.