JP2014220172A - Wrapping material for battery - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a wrapping material for battery having high insulation properties which can maintain a state of sealing a battery element without cleavage until reaching a set temperature determined between 140°C and 160°C, and can unseal quickly and gently at a moment in time when reaching a set temperature, while suppressing excessive expansion and runaway of cell reaction.SOLUTION: A wrapping material for battery consists of a laminate having at least a base material layer, an adhesive layer, a metal layer, an insulation layer, and a sealant layer in this order. The insulation layer is formed of a resin composition containing an acid modified polyolefin resin and a hardener, the sealant layer has a first sealant layer containing polyolefin resin, and the melting points of the insulation layer and sealant layer satisfy a predetermined relationship.

Description

  The present invention relates to a battery packaging material that can ensure safety even when the pressure and temperature in the battery are continuously increased, and further has high insulation properties. More specifically, the present invention does not open until a set temperature determined between 140 and 160 ° C. is reached, the battery element can be maintained in a sealed state, and when the set temperature is reached, the battery element is quickly opened. In addition, the present invention relates to a battery packaging material that can be opened gently to suppress excessive expansion of the battery packaging material and runaway battery reaction, and further has excellent insulation properties.

  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.

  On the other hand, depending on the type of electrolyte, the battery may generate a combustible gas and the pressure may increase. For example, when the battery is exposed to a high temperature, the organic solvent used in the electrolytic solution may be decomposed to generate a combustible gas and cause an increase in pressure. In addition, the battery may continuously increase in temperature due to charging due to overvoltage or discharging due to excessive current, causing battery reaction to runaway.

  In a battery using a film-like battery packaging material, such an increase in the pressure or temperature in the battery may cause the battery packaging material to be cleaved and cause ignition due to ejection of combustible gas. Further, if the pressure or temperature rises continuously in the battery and the battery reaction runs out of control when the battery packaging material is excessively expanded, the battery may explode.

  Conventionally, as a packaging material for a battery that can suppress the tearing of the heat seal part and the break before the heat seal part even when the pressure in the battery rises continuously, the sealant layer or adjacent thereto It has been reported that one of the adhesive resin layers has a cleavage inducing portion in which the stress at the time of cleavage is smaller than the stress at the time of cleavage of the fused surface between the sealant layers (see Patent Document 2). However, Patent Document 2 is not designed to be opened gently when the pressure or temperature in the battery has been continuously increased. In fact, in Patent Document 2, when a strong stress is applied, delamination in which cleavage proceeds between layers having adhesiveness, or cohesive failure in which cracks progress in an adhesive layer occurs. Designed to be If the battery is opened by delamination or cohesive failure when the pressure or temperature in the battery rises, there is a concern that the risk of ignition, explosion, or the like may increase due to a sudden ejection of combustible gas.

  Therefore, the battery packaging material is not cleaved until it reaches about 140 to 160 ° C. in order to ensure safety when the pressure or temperature rise in the battery continuously proceeds, and the battery element By maintaining the sealed state, the gas in the battery packaging material is gradually opened by gradually opening the gas when the temperature reaches about 140 to 160 ° C., while suppressing the ignition due to the sudden ejection of the combustible gas. It is required to be designed to release.

  Depending on the type and application of the battery, the temperature that should be induced to open from the maintenance of the battery packaging material is different, so the battery packaging material needs to be designed for sealing and unsealing depending on the applied battery. There is. For example, if there is a battery that is required to be induced from a sealed state to an opened state when reaching 140 ° C., there is a battery that is required to be induced from the sealed state to the opened state when reaching 160 ° C. Therefore, in the prior art, the current situation is that the battery packaging material must be individually designed according to the temperature to be guided from the maintenance of the sealing to the opening, and the setting determined between 140 and 160 ° C. Regarding battery packaging materials that are induced to open from maintaining a sealed state at a temperature, a common design guideline that does not depend on the difference in the set temperature is not disclosed.

  Further, in the battery manufacturing process, minute foreign matters such as electrode active material and electrode tab fragments may adhere to the surface of the sealant layer, and the heat generated when the battery element is heat sealed with the battery packaging material. Depending on the pressure, the portion of the sealant layer to which foreign matter has adhered may become thin. For example, when the sealant layer becomes thin in a portion where the sealant layers are heat-sealed, there is a problem that the insulation of the battery packaging material may be insufficient.

  Minute foreign matters such as electrode active materials and electrode tab fragments generally have electrical conductivity. If conductive foreign matter exists between the electrode tab and the sealant layer, the foreign material penetrates the sealant layer due to heat and pressure during heat sealing, and the electrode tab and the metal layer of the battery packaging material are electrically connected. There is a risk of short circuiting.

JP 2001-202927 A JP 2012-203982 A

  The present invention has been made in view of the above problems of the prior art. More specifically, according to the present invention, the battery element can be maintained in a sealed state without being cleaved until reaching a set temperature determined between 140 and 160 ° C., and when the set temperature is reached. It can be opened quickly and gently, suppressing excessive expansion of battery packaging materials and runaway battery reaction. In addition, minute foreign substances such as electrode active material and electrode tab debris are separated from the interface between the sealant layers and the electrode tab. The main object is to provide a battery packaging material having high insulation even when present in a heat-sealed portion such as between a sealant layer and the like.

The present inventor has conducted intensive studies to solve the above-mentioned problems.As a result, the inventor comprises a laminate having at least a base material layer, an adhesive layer, a metal layer, an insulating layer, and a sealant layer in this order. It is formed with the resin composition containing modified polyolefin resin and a hardening | curing agent, a sealant layer has the 1st sealant layer containing polyolefin resin, and an insulating layer and a 1st sealant layer are following formula (1) and (2 The battery packaging material satisfying the relationship) reaches T ° C. when the temperature is raised to a set temperature T ° C. determined between 140 ° C. and 160 ° C. at an internal pressure of 1 atm and a heating rate of 3 ° C./min. Until then, at least a part of the interface between the metal layer and the insulating layer is peeled off, but the battery element can be kept sealed by the insulating layer and the sealant layer, and the metal layer can be quickly reached after reaching T ° C. Peeled from Found that can open gently causing min insulating layer and fine cleavage of pinholes in the sealant layer. Furthermore, it has also been found that such a battery packaging material has high insulating properties. The present invention has been completed by further studies based on such knowledge.
−10 ≦ T _A −T ≦ −5 (1)
−5 ≦ T ₁ −T ≦ 5 (2)
T _A : melting point (° C.) of the insulating layer
T ₁ : Melting point (° C.) of the first sealant layer

That is, this invention provides the invention of the aspect hung up below.
Item 1. When the temperature is raised to a set temperature T ° C determined between 140 ° C and 160 ° C, the packaging material is not opened until the temperature reaches T ° C. After reaching T ° C, the packaging material is opened quickly. A battery packaging material used for a battery,
It consists of a laminate having at least a base material layer, an adhesive layer, a metal layer, an insulating layer, and a sealant layer in this order,
The insulating layer is formed of a resin composition containing an acid-modified polyolefin resin and a curing agent,
The sealant layer has a first sealant layer containing a polyolefin resin,
The insulating layer and the first sealant layer are represented by the following formulas (1) and (2):
−10 ≦ T _A −T ≦ −5 (1)
−5 ≦ T ₁ −T ≦ 5 (2)
T _A : melting point (° C.) of the insulating layer
T ₁ : Melting point (° C.) of the first sealant layer
Battery packaging material that satisfies this relationship.
Item 2. The acid-modified polyolefin resin in the insulating layer was modified with an acid-modified polyolefin resin modified with an unsaturated carboxylic acid or an acid anhydride thereof, and an unsaturated carboxylic acid or acid anhydride and a (meth) acrylic acid ester. Item 2. The battery packaging material according to Item 1, which is at least one of acid-modified polyolefin resins.
Item 3. The acid-modified polyolefin resin modified with the unsaturated carboxylic acid or acid anhydride thereof is formed by modifying at least one of a polyethylene resin or a polypropylene resin with the unsaturated carboxylic acid or acid anhydride thereof. Item 3. A battery packaging material according to Item 2.
Item 4. The acid-modified polyolefin resin modified with the unsaturated carboxylic acid or acid anhydride thereof and a (meth) acrylic acid ester is such that at least one of a polyethylene resin and a polypropylene resin is the unsaturated carboxylic acid or acid anhydride thereof. Item 3. The battery packaging material according to Item 2, which is modified with (meth) acrylic acid ester.
Item 5. Item 5. The battery packaging material according to any one of Items 1 to 4, wherein the polyolefin resin contained in the first sealant layer contains at least propylene as a constituent monomer.
Item 6. Item 6. The battery packaging material according to any one of Items 1 to 5, wherein the insulating layer has a thickness of 0.1 to 20 µm, and the first sealant layer has a thickness of 1 to 40 µm.
Item 7. Item 7. The battery packaging material according to any one of Items 1 to 6, wherein the metal layer is an aluminum foil.
Item 8. Item 8. The battery packaging material according to any one of Items 1 to 7, wherein the curing agent includes at least one selected from the group consisting of a polyfunctional isocyanate compound, a carbodiimide compound, an epoxy compound, and an oxazoline compound.
Item 9. The said resin composition WHEREIN: Content of the said hardening | curing agent exists in the range of 0.1 mass part-50 mass parts with respect to 100 mass parts of said acid-modified polyolefin resin, The term in any one of claim | item 1-8. Battery packaging material.
Item 10. The sealant layer further includes a second sealant layer including at least one of an acid-modified polyolefin resin and a polyolefin resin between the insulating layer and the first sealant layer, and the second sealant layer is represented by the following formula (3 )
5 ≦ T ₂ −T ≦ 10 (3)
T ₂ : Melting point (° C.) of the second sealant layer
Item 10. The battery packaging material according to any one of Items 1 to 9, wherein
Item 11. Item 11. The battery packaging material according to Item 10, wherein the acid-modified polyolefin resin and the polyolefin resin in the second sealant layer contain at least propylene as a constituent monomer.
Item 12. Item 12. A battery in which a battery element including at least a positive electrode, a negative electrode, and an electrolyte is accommodated in the battery packaging material according to any one of Items 1 to 11.

  According to the battery packaging material of the present invention, by adopting such a specific configuration, when the temperature is raised to a predetermined temperature between 140 to 160 ° C. at an internal pressure of 1 atm and a temperature rising rate of 3 ° C./min. In addition, until the predetermined temperature is reached, at least a part of the interface between the metal layer and the insulating layer peels off, but the insulating layer and the sealant layer are formed in a bag shape and the battery element can be kept sealed. In addition, the battery packaging material of the present invention, after reaching a predetermined temperature, quickly causes a minute opening such as pinholes in the insulating layer and sealant layer separated from the metal layer, and is opened in a mild condition. Can be. Thus, the battery packaging material of the present invention does not cleave until reaching a predetermined temperature between 140 and 160 ° C., can maintain the battery element in a sealed state, and when it reaches the predetermined temperature. Because it can be opened quickly and gently, even if the pressure and temperature in the battery continue to rise, excessive expansion of the battery packaging material and runaway battery reaction can be suppressed, ensuring safety. The

  Furthermore, according to the battery packaging material of the present invention, minute foreign matters such as electrode active material and electrode tab fragments are exposed to heat-sealed portions such as the interface between the sealant layers and between the electrode tab and the sealant layer. Even when it exists, it is possible to provide a battery packaging material having high insulation. Furthermore, since the battery packaging material of the present invention has high adhesion between the insulating layer and the metal layer or sealant layer, the battery packaging material is also excellent in durability. That is, by sealing the battery element with the battery packaging material of the present invention, the insulation of the battery can be improved, and the durability of the battery can be improved.

It is a figure which shows an example of the cross-section of the packaging material for batteries of this invention. A state (A) in which two battery packaging materials of the present invention are heat-sealed to form a sealed space, and when the temperature is raised to a set temperature T ° C. determined between 140 ° C. and 160 ° C., the set temperature T ° C. It is sectional drawing (the left end is heat-sealed and the right side part is abbreviate | omitted) of one side about the state (B) before reaching | attainment, and the state (C) after reaching preset temperature T degreeC. It is a schematic diagram which shows the cleaved state which arises when two conventional packaging materials for batteries are heat-sealed to form a sealed space and heated to a set temperature T ° C determined between 140 ° C and 160 ° C.

A. Battery packaging material The battery packaging material of the present invention does not open until the temperature reaches T ° C. when the temperature is raised to a set temperature T ° C. determined between 140 ° C. and 160 ° C., and reaches T ° C. And a battery packaging material used for a battery packaging material used for a battery set so that the packaging material can be opened quickly; at least a base material layer, an adhesive layer, a metal layer, an insulating layer, And the insulating layer is formed of a resin composition containing an acid-modified polyolefin resin and a curing agent; the sealant layer has a first sealant layer containing a polyolefin resin. And the melting points of the insulating layer and the first sealant layer satisfy a predetermined relationship. Hereinafter, the battery packaging material of the present invention will be described in detail.

1. As shown in FIG. 1, the battery packaging material is made of a laminate having at least a base layer 1, an adhesive layer 2, a metal layer 3, an insulating layer 4, and a sealant layer 5 in this order. Thus, the sealant layer 5 has a first sealant layer 5a. That is, the battery packaging material of the present invention is composed of a laminate having the base layer 1, the adhesive layer 2, the metal layer 3, the insulating layer 4, and the first sealant layer 5a in this order. 1 is the outermost layer, and the first sealant layer 5a is the innermost layer. At the time of assembling the battery, the battery elements are sealed by sealing the battery elements by bringing the first sealant layers 5a located on the periphery of the battery elements into contact with each other and thermally welding them. The sealant layer 5 may be formed of a plurality of layers. For example, the second sealant layer 5b and the third sealant layer 5c may be provided between the first sealant layer 5a and the insulating layer 4 as necessary. You may have in order.

2. Opening mechanism of battery packaging material The battery packaging material of the present invention has a sealing property until reaching a set temperature T ° C defined between 140 ° C and 160 ° C, and a quick and gentle after reaching the set temperature T ° C. It has a good openability. An example of the opening mechanism of the battery packaging material of the present invention will be described with reference to FIG. FIG. 2A shows a cross-sectional view of one side when a battery element is sealed in two battery packaging materials of the present invention. In FIG. 2A, the edges of the two sealant layers 5 of the battery packaging material are heat-sealed to form a sealed space. Although the battery element is accommodated in the sealed space, the battery element is omitted in FIG. When the temperature is raised from the state of FIG. 2A to a set temperature T.degree. C. determined between 140.degree. C. and 160.degree. C., as shown in FIG. Although it peels off, the insulating layer 4 and the sealant layer 5 are formed in a bag shape (inner bag shape) and the battery element is kept sealed. When the temperature reaches the set temperature T ° C., the state quickly shifts to the state shown in FIG. 2C, and fine cracks such as pinholes are formed in the regions of the insulating layer 4 and the sealant layer 5 separated from the metal layer 3 (in FIG. 2). (Indicated by reference numeral 10) and the unsealed state is obtained under mild conditions. In the battery packaging material of the present invention, when the temperature is raised to a set temperature T ° C. determined between 140 and 160 ° C., at least a part of the interface between the insulating layer 4 and the sealant layer 5 is peeled off, The sealant layer 5 may be formed into a bag shape, and then, the sealant layer 5 may be finely cleaved such as pinholes to be opened in a mild condition.

  On the other hand, conventional battery packaging materials are opened quickly after reaching the set temperature T ° C without being opened quickly, or are opened quickly before or after reaching the set temperature T ° C. It may shift rapidly and cause a swift ejection of combustible gas or electrolyte. This abrupt transition from the sealed state to the unsealed state is caused by the transition to any one of interface peeling, cohesive peeling, and delamination. Here, interfacial peeling refers to a peeling state in which cleavage proceeds at the heat seal interface between the sealant layers, and an example of the schematic diagram is shown in FIG. Moreover, cohesive peeling refers to the peeling state in which the cleavage proceeds inside the sealant layer, and an example of the schematic diagram is shown in FIG. In addition, delamination refers to a delamination state in which cleavage progresses between layers (layers within a sealant layer or between a metal layer and a sealant layer) after the sealant layer is broken, and an example of a schematic diagram thereof Is shown in FIG. The “root break” means that the sealant layer is broken at the inner edge of the heat seal portion. Since the battery packaging material of the present invention does not cause such interfacial peeling, cohesive peeling, or delamination to shift to an abrupt opening state, the battery packaging material in the battery has a higher capacity than conventional battery packaging materials. Excellent safety when pressure and temperature rise continuously.

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.

  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 resin films 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 , Polyimide resin, amino resin, rubber, and silicon resin.

  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 preferably used 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 for bonding the base material layer 1 and the metal layer 3 together.

  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. Further, 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, and a hot pressure type.

  Specific examples of adhesive resins that can be used to form the adhesive layer 2 include polyester resins such as polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, polybutylene naphthalate, polyethylene isophthalate, polycarbonate, and copolyester. 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, amino resin such as melamine resin; Chloroprene rubber, Nitrile rubber, Styrene rubber Silicone resin; rubber such diene 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 5 side, and more preferably both surfaces in order to stabilize adhesion, prevent 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. In the general formulas (1) to (4), X is preferably any one of a hydrogen atom, a hydroxyl group, and a hydroxyalkyl 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 layer on the surface of the metal layer 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.

In the chemical conversion treatment, the amount of the acid-resistant film to be formed on the surface of the metal layer 3 is not particularly limited. For example, when the chromate treatment is performed by combining a chromic acid compound, a phosphoric acid compound, and an aminated phenol polymer. For example, 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. 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 by a bar coating method, a roll coating method, a gravure coating method, an immersion method or the like, and then the temperature of the metal layer is 70. It is carried out by heating to about 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.

[Insulating layer 4]
In the present invention, the insulating layer 4 is a layer provided between the metal layer 3 and the sealant layer 5. The insulating layer 4 is formed of a resin composition containing an acid-modified polyolefin resin and a curing agent. In the battery packaging material of the present invention, since the insulating layer 4 formed of such a specific resin composition is provided between the metal layer 3 and the sealant layer 5, the electrode active material and the electrode tab are provided. Even when a minute foreign matter such as a broken piece is present between the battery element and the sealant layer 5, the insulation and durability of the battery packaging material are enhanced.

  Although it does not restrict | limit especially as acid-modified polyolefin resin which forms the insulating layer 4, Acid-modified polyolefin resin modified with unsaturated carboxylic acid or its acid anhydride, and unsaturated carboxylic acid or its acid anhydride, and (meth) It is preferably at least one of acid-modified polyolefin resins modified with an acrylic ester. Here, the acid-modified polyolefin resin modified with an unsaturated carboxylic acid or an acid anhydride thereof is obtained by modifying a polyolefin resin with an unsaturated carboxylic acid or an acid anhydride thereof. The acid-modified polyolefin resin modified with an unsaturated carboxylic acid or its acid anhydride and (meth) acrylic acid ester is a combination of an unsaturated carboxylic acid or its acid anhydride and (meth) acrylic acid ester. Thus, it is obtained by modifying the polyolefin resin. In the present invention, “(meth) acrylic acid ester” means “acrylic acid ester” or “methacrylic acid ester”.

  The polyolefin resin to be modified is not particularly limited as long as it is a resin containing at least an olefin as a monomer unit. The polyolefin resin can be composed of, for example, at least one of a polyethylene resin and a polypropylene resin, and is preferably composed of a polypropylene resin. The polyethylene resin can be composed of, for example, at least one of homopolyethylene and ethylene copolymer. The polypropylene resin can be composed of at least one of a homopolypropylene and a propylene copolymer, for example. Examples of the propylene copolymer include copolymers of propylene and other olefins such as an ethylene-propylene copolymer, a propylene-butene copolymer, and an ethylene-propylene-butene copolymer. The proportion of the propylene unit contained in the polypropylene resin is preferably about 50 mol% to 100 mol%, more preferably about 80 mol% to 100 mol%, from the viewpoint of further improving the insulation and durability of the battery packaging material. More preferably. In addition, the proportion of ethylene units contained in the polyethylene resin is preferably about 50 mol% to 100 mol%, and more preferably 80 mol% to 100 mol, from the viewpoint of further improving the insulation and durability of the battery packaging material. More preferably, it is about%. Each of the ethylene copolymer and the propylene copolymer may be a random copolymer or a block copolymer. Further, the ethylene copolymer and the propylene copolymer may each be crystalline or amorphous, and may be a copolymer or a mixture thereof. The polyolefin resin may be formed of one type of homopolymer or copolymer, or may be formed of two or more types of homopolymer or copolymer.

  Examples of the unsaturated carboxylic acid include acrylic acid, methacrylic acid, maleic acid, itaconic acid, fumaric acid, and crotonic acid. Moreover, as an acid anhydride, the acid anhydride of the unsaturated carboxylic acid illustrated above is preferable, and maleic anhydride and itaconic anhydride are more preferable. In the modification of the polyolefin resin, only one type of unsaturated carboxylic acid may be used, or two or more types may be used.

  Examples of the (meth) acrylic acid ester include an esterified product of (meth) acrylic acid and an alcohol having 1 to 30 carbon atoms, preferably an esterified product of (meth) acrylic acid and an alcohol having 1 to 20 carbon atoms. Is mentioned. Specific examples of (meth) acrylic acid esters include methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate, hexyl (meth) acrylate, (meth) Examples include octyl acrylate, decyl (meth) acrylate, lauryl (meth) acrylate, octyl (meth) acrylate, dodecyl (meth) acrylate, stearyl (meth) acrylate, and the like. In modification | denaturation of polyolefin resin, only 1 type may be used for (meth) acrylic acid ester and it may use 2 or more types.

  The ratio of the unsaturated carboxylic acid or its acid anhydride in the acid-modified polyolefin resin is preferably about 0.1% by mass to 30% by mass, and preferably about 0.1% by mass to 20% by mass. Is more preferable. By setting it as such a range, the insulation and durability of the packaging material for batteries can be improved more.

  Further, the proportion of (meth) acrylic acid ester in the acid-modified polyolefin resin is preferably about 0.1% by mass to 40% by mass, and more preferably about 0.1% by mass to 30% by mass. . By setting it as such a range, the insulation and durability of the packaging material for batteries can be improved more.

  The weight average molecular weight of the acid-modified polyolefin resin is preferably about 6000 to 200000, more preferably about 8000 to 150,000. By setting it as such a range, since the affinity of the insulating layer 4 with respect to the metal layer 3 and the sealant layer 5 can be stabilized, the adhesiveness of the metal layer 3 and the sealant layer 5 can be stabilized for a long time. Furthermore, since heat resistance can also be improved, the insulation and durability of the battery packaging material can be further improved. The weight average molecular weight of the acid-modified polyolefin resin is a value measured by gel permeation chromatography (GPC) measured under conditions using polystyrene as a standard sample.

  In the acid-modified polyolefin resin, the method for modifying the polyolefin resin is not particularly limited, and for example, an unsaturated carboxylic acid or an acid anhydride thereof or a (meth) acrylic acid ester may be copolymerized with the polyolefin resin. Examples of such copolymerization include random copolymerization, block copolymerization, graft copolymerization (graft modification), and the like, and preferably graft copolymerization.

  The curing agent is not particularly limited as long as it cures the acid-modified polyolefin resin. 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):

A polycarbodiimide compound having a repeating unit represented by:
The following general formula (6):

A polycarbodiimide compound having a repeating unit represented by:
And the following general formula (7):

The polycarbodiimide compound represented by these is mentioned. In general formula (5)-(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 insulating layer 4, the curing agent may be composed of two or more kinds of compounds.

  In the resin composition, the content of the curing agent is preferably in the range of 0.1 to 50 parts by mass with respect to 100 parts by mass of the acid-modified polyolefin resin, and 0.1 to 30 parts by mass. More preferably, it is in the range. In the resin composition, 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 the acid-modified polyolefin resin. More preferably, it is in the range of ˜20 equivalents. Thereby, the insulation and durability of the battery packaging material can be further improved.

  Further, by adding an olefin rubber-like additive or a hydrocarbon wax to the insulating layer 4, the insulating layer 4 has a high flexibility, and it is possible to suppress crushing at the time of foreign matter biting due to stress dispersion during compression, It is possible to prevent fine cracks during stretching. Examples of the olefinic rubber-like additive include Mitsui Chemicals' Tuffmer P, Tuffmer A, Tuffmer H, Tuffmer XM, Tuffmer BL, Tuffmer PN, and α-olefin copolymers such as Sumitomo Chemical's Tough Selenium. Examples of the hydrocarbon wax include paraffin.

  As described above, in the manufacturing process of the battery, minute foreign matters such as electrode active material and electrode tab fragments may adhere to the surface of the sealant layer, which causes a thin-walled portion or a through hole in the sealant layer, There is a possibility that the insulating property is lowered. On the other hand, the battery packaging material of the present invention is formed from the resin composition containing the acid-modified polyolefin resin and the curing agent as described above, and has high heat resistance and mechanical properties when heat is applied during heat sealing. The insulating layer 4 is formed which has strength, high flexibility, and can suppress generation of fine cracks due to stress such as bending. For this reason, in the sealant layer 5, fine cracks that are likely to occur in thin portions, through-holes due to foreign matters, and voids due to foaming of the sealant layer 5 that are generated when the sealant layer 5 is heat-sealed in a state where it is bitten are formed. In this case, the insulating layer 4 can prevent the electrolytic solution from coming into direct contact with the metal layer, and the metal layer 3 is protected. In addition, even when the sealant layer 5 bites foreign matter or the like, the insulating layer 4 having high heat resistance and high mechanical strength and flexibility can prevent deterioration of the insulating property of the battery packaging material due to foreign matter.

Moreover, in addition to being formed with the resin composition containing an acid-modified polyolefin resin and a hardening | curing agent, the insulating layer 4 is set so that the relationship of following formula (1) may be satisfied.
−10 ≦ T _A −T ≦ −5 (1)
T: Set temperature (° C) determined between 140 and 160 ° C
T _A : melting point of the insulating layer (° C.)

By thus setting the melting point T _A of the insulating layer 4 to a low value within a predetermined range than the set temperature T, when the battery is exposed to high temperatures up to T ° C., the insulating layer 4 is in a molten state Thus, at least a part of the insulating layer 4 can be peeled off from the interface between the metal layer 3 and the insulating layer 4. Then, at least a part of the insulating layer 4 peeled off from the metal layer 3 is expanded by an internal pressure together with a sealant layer 5 to be described later, and swells while maintaining a sealed state. Thereafter, the swollen insulating layer 4 and the sealant layer 5 are T Fine cleavage (pinholes, etc.) occurs within 30 minutes after reaching the temperature, and the gas inside the battery can be released gently.

Here, the melting point T _A of the insulating layer 4, the melting point of the resin constituting the insulating layer 4 JIS K6921-2: a value measured by compliant DSC method (ISO1873-2.2 95). In addition, when the insulating layer 4 is formed of a blend resin containing a plurality of resins, the melting point T _A of the blend resin conforms to JIS K6921-2 (ISO 1873-2.2: 95) and DSC. Calculate the ratio of the peak area of the melting point corresponding to each resin with the total peak area being 1, and calculate the value (melting point x area ratio) multiplied by the ratio of the melting point corresponding to each resin and the peak area ratio. Further, it is obtained by adding the value (melting point × area ratio) calculated for each melting point.

  Since the melting point of the resin is determined by the molecular weight, the type and ratio of the constituent monomer, etc., the acid-modified polyolefin resin blended in the insulating layer 4 has its molecular weight and constituent monomer so as to satisfy the melting point range of the insulating layer 4. The type and ratio are set as appropriate.

  Although the thickness of the insulating layer 4 will not be specifically limited if it is the thickness suitable for the packaging material for batteries, For example, about 0.1 micrometer-20 micrometers, Preferably it can be set as about 0.5 micrometer-15 micrometers. Since the battery packaging material of the present invention is molded into various shapes according to the shape of the battery, a certain degree of flexibility is also required. In the battery packaging material, by setting the thickness of the insulating layer 4 in such a range, the insulation and durability can be further improved while maintaining the flexibility of the battery packaging material.

  The insulating layer 4 may have a multilayer structure of two or more layers. Thereby, even when a thin-walled portion or a through-hole is formed in the first insulating layer together with the sealant layer 5, the insulating properties can be maintained by the second and third insulating layers.

[Sealant layer]
In the battery packaging material of the present invention, the sealant layer 5 corresponds to the innermost layer, and is a layer that heat-welds the sealant layers 5 together during battery assembly to seal the battery element. The sealant layer 5 has a first sealant layer 5a containing a polyolefin resin. The sealant layer 5 may be formed of a plurality of layers. If necessary, the sealant layer 5 includes at least one of an acid-modified polyolefin resin and a polyolefin resin in order from the first sealant layer 5a side to the metal layer 3 side. You may have the 2nd sealant layer 5b, the 3rd sealant layer 5c containing at least one of acid-modified polyolefin resin and polyolefin resin. When the sealant layer 5 is formed of a plurality of layers, the battery has a layer structure in which the first sealant layer 5a containing a polyolefin resin is located in the innermost layer of the battery packaging material when the battery is assembled.

(First sealant layer)
The 1st sealant layer 5a is a layer which contains polyolefin resin and is located in the innermost layer of the battery packaging material. The polyolefin resin used for forming the first sealant layer 5a is not particularly limited as long as the melting point described below is satisfied, and examples thereof include low density polyethylene, medium density polyethylene, high density polyethylene, and linear low density polyethylene. Polypropylene such as homopolypropylene, block copolymer of polypropylene (for example, block copolymer of propylene and ethylene), random copolymer of polypropylene (for example, random copolymer of propylene and ethylene), etc., polypropylene of ethylene or ethylene-butene -Propylene terpolymer and the like. Among these polyolefins, from the viewpoint of heat resistance, a polyolefin having at least propylene as a constituent monomer is preferable, more preferably a random copolymer of propylene-ethylene, a terpolymer of propylene-ethylene-butene, and a homopolymer of propylene. Can be mentioned. These polyolefin resins may be used individually by 1 type, and may be used in combination of 2 or more type.

  The 1st sealant layer 5a may be formed only from polyolefin resin, and may contain resin other than polyolefin resin as needed. When the resin other than the polyolefin resin is contained in the first sealant layer 5a, the content of the polyolefin in the first sealant layer 5a is not particularly limited as long as the effect of the present invention is not hindered, for example, 10 to 95% by mass, Preferably 30-90 mass%, Furthermore, 50-80 mass% is mentioned.

  In addition to the polyolefin resin in the first sealant layer 5a, examples of the resin that can be contained as necessary include an acid-modified polyolefin resin. Examples of the acid-modified polyolefin resin include polymers obtained by graft polymerization of the polyolefin resin exemplified in the first sealant layer 5a with an unsaturated carboxylic acid or an acid anhydride thereof. Examples of the unsaturated carboxylic acid or acid anhydride thereof 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.

  When the resin other than the polyolefin resin is contained in the first sealant layer 5a, the content of the resin is appropriately set within a range that does not hinder the object of the present invention. For example, when the acid-modified polyolefin resin is contained in the first sealant layer 5a, the content of the acid-modified polyolefin resin in the first sealant layer 5a is usually 5 to 60% by mass, preferably 10 to 50% by mass, Preferably 20-40 mass% is mentioned.

The first sealant layer 5a is set so as to satisfy the following formula (2) in addition to including the polyolefin resin.
−5 ≦ T ₁ −T ≦ 5 (2)
T: Set temperature (° C.) determined between 140 ° C. and 160 ° C.
T ₁ : Melting point (° C.) of the first sealant layer

Thus the melting point T ₁ of the first sealant layer 5a is set to higher than the melting point T _A of the insulating layer 4, and by setting the temperature range of the set temperature T and 5 ° C. before and after the battery set temperature T ° C. When the insulating layer 4 and the sealant layer 5 are swollen in a sealed state when at least a part of the insulating layer 4 is peeled off from the interface between the metal layer 3 and the insulating layer 4 due to exposure to high temperatures, the insulating layer 4 and the sealant Suppresses the cracks from advancing inside the layer 5 and suddenly opening due to cohesive failure, causing fine cracks (pinholes, etc.). It becomes possible to release. If the melting point T ₁ of the first sealant layer 5a is set in a temperature range that exceeds 5 ° C. from the set temperature T, heat sealing itself becomes difficult, and even if the sealing strength varies or reaches T ° C., it is quick. There is a tendency that the sealant layer 5 cannot be opened.

The method for calculating the melting point T ₁ of the first sealant layer 5 a is the same as that for the melting point T _A of the insulating layer 4.

  Since the melting point of the resin is determined by the molecular weight, the type and ratio of the constituent monomers, etc., the polyolefin resin blended in the first sealant layer 5a and other resins blended as necessary have the melting point of the first sealant layer 5a. The molecular weight, the type and ratio of constituent monomers, etc. are appropriately set so as to satisfy the range.

  Examples of the thickness of the first sealant layer 5a include 5 to 40 μm, preferably 10 to 35 μm, and more preferably 15 to 30 μm.

(Relationship between melting point of insulating layer and first sealant layer)
The insulating layer 4 and the first sealant layer 5a satisfy the relationship of 0 ≦ (T ₁ −T _A ) ≦ 15 by satisfying the above-described melting points.

(Second sealant layer)
The second sealant layer 5b is a layer provided between the first sealant layer 5a and the insulating layer 4 as necessary when the sealant layer 5 is formed of multiple layers. The second sealant layer 5b includes at least one of a polyolefin resin and an acid-modified polyolefin. Examples of the polyolefin resin and the acid-modified polyolefin used for forming the second sealant layer are the same as those exemplified in the first sealant layer 5a.

  The second sealant layer 5b may be formed of only one of the acid-modified polyolefin resin and the polyolefin resin as long as it has a melting point described later, and may contain other resins as necessary. Good. When the second sealant layer 5b contains an acid-modified polyolefin, the content of the acid-modified polyolefin resin in the second sealant layer 5b is not particularly limited as long as the effect of the present invention is not hindered, for example, 5 to 95% by mass, Preferably it is 10-90 mass%, Furthermore, 20-80 mass% is mentioned. In addition, when the second sealant layer 5b contains a polyolefin resin, the content of the polyolefin resin in the second sealant layer 5b is not particularly limited as long as the effect of the present invention is not hindered. 10-90 mass%, Furthermore, 20-80 mass% is mentioned.

Moreover, the 2nd sealant layer 5b is set so that following formula (3) may be satisfied.
5 ≦ T ₂ −T ≦ 10 (3)
T: Set temperature (° C.) determined between 140 ° C. and 160 ° C.
T ₂ : Melting point (° C.) of the second sealant layer

Thus the melting point T ₂ of the second sealant layer is set above the melting point T _A of the insulating layer, and by setting the high temperature range of 5 ° C. to 10 ° C. than the set temperature T, the battery set temperature T ° C. The second sealant layer 5b swells with the internal pressure even if the insulating layer 4 is exposed to a high temperature until the insulating layer 4 is melted and at least a part of the insulating layer 4 is peeled off from the interface between the metal layer 3 and the insulating layer 4. However, after the set temperature T ° C. is reached, fine cleaving (pinholes or the like) can be quickly generated, and the gas inside the battery can be released gently. Furthermore, since the melting point T ₂ of the second sealant layer 5b is set to be equal to or higher than the melting point T _A of the insulating layer 4 and equal to or higher than the melting point T ₁ of the first sealant layer, the temperature is raised to the set temperature T ° C. Even in such a case, an excellent insulating property can be provided.

The method for calculating the melting point T ₂ of the second sealant layer 5 b is the same as that for the melting point T _A of the insulating layer 4.

  Since the melting point of the resin is determined by the molecular weight, the type and ratio of the constituent monomers, etc., the acid-modified polyolefin blended in the second sealant layer 5b and other resins blended as necessary are the melting points of the second sealant layer 5b. The molecular weight, the type and ratio of constituent monomers, etc. are appropriately set so as to satisfy this range.

  Moreover, as thickness of the 2nd sealant layer 5b, 5-40 micrometers, Preferably it is 10-35 micrometers, More preferably, 15-30 micrometers is mentioned, for example.

(Relationship between melting points of insulating layer and second sealant layer)
The insulating layer 4 and the second sealant layer 5b satisfy the relationship of 10 ≦ (T ₂ −T _A ) ≦ 20 by satisfying the above-described melting points.

(3rd sealant layer)
The third sealant layer 5c is a layer provided between the second sealant layer 5b and the insulating layer 4 as necessary when the sealant layer 5 is formed of multiple layers. The third sealant layer 5c is formed of the same resin as the second sealant layer 5b. Further, the melting point, thickness, etc. of the third sealant layer 5c can be the same as those of the second sealant layer 5b.
(Thickness of sealant layer 5)
The thickness of the sealant layer 5 is determined based on the thickness of each of the first sealant layer 5a, the second sealant layer, the third sealant layer, and the like provided as necessary. For example, the thickness is 15 to 120 μm, preferably 60 -80 μm, more preferably 30-60 μm.

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 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 above resin composition used for forming the insulating layer 4 is applied on the metal layer 3 of the laminate A and dried. The resin composition can be applied by a coating method such as a gravure coating method or a roll coating method. Next, the sealant layer 5 is laminated on the insulating layer 4. The lamination of the sealant layer 5 on the insulating layer 4 can be performed, for example, by a method of applying the first sealant layer on the insulating layer 4 by a method such as a gravure coating method or a roll coating method. Before laminating the first sealant layer on the insulating layer 4, a third sealant layer, a second sealant layer, and the like may be laminated on the insulating layer 4 by a similar method, if necessary. Alternatively, the sealant layer 5 can be laminated on the insulating layer 4 by a method of extruding the first sealant layer on the insulating layer 4. For example, when providing a 2nd sealant layer etc., the method of coextruding a 2nd sealant layer etc. and a 1st sealant layer is also employable. For example, after applying or thermocompression bonding the second sealant layer or the like on the insulating layer 4, the first sealant layer may be extruded, or the third sealant layer is applied or thermocompression bonded on the insulating layer 4. Later, the second sealant layer and the first sealant layer may be coextruded. Furthermore, after coextruding the third sealant layer and the second sealant layer on the insulating layer 4, the first sealant layer may be applied or thermocompression-bonded, or the third sealant layer may be formed on the insulating layer 4. After the extrusion, the second sealant layer and the first sealant layer may be sequentially applied or thermocompression-bonded.

  As described above, a laminate composed of the base material layer 1 / adhesive layer 2 / metal layer 3 / insulating layer 4 / sealant layer 5 whose surface is subjected to chemical conversion treatment as necessary is formed. In order to strengthen the adhesiveness, 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 second 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. Characteristics and Applications of Battery Packaging Material The battery packaging material of the present invention has the specific insulating layer and the sealant layer described above, so that the sealed space is formed in a state where the sealant layers are heat sealed to form a sealed space. Is exposed to heating conditions in which the temperature is increased by 1 atm higher than the outside to a set temperature T ° C determined between 140 and 160 ° C at a rate of temperature increase of 3 ° C / min, until T ° C is reached. The packaging material does not open, and the packaging material can be opened within 30 minutes after reaching T ° C. More specifically, the battery packaging material of the present invention does not open the packaging material until the set temperature T ° C. defined between 140 to 160 ° C. is reached under the heating conditions shown below. It becomes possible to provide the property of opening within 30 minutes after reaching ° C.
<Heating conditions>
(1) A recess having a depth of 3 mm, a length of 35 and a width of 50 mm is formed at the center of the battery packaging material cut into a shape having a length of 80 mm and a width of 150 mm, and is formed into a shape having an edge around the recess. Two battery packaging materials molded into such a shape are prepared.
(2) The edge portions are overlapped so that the two sealant layers of the battery packaging material formed as described above face each other, and the edge portions are heat sealed (175 ° C., 3 seconds, surface pressure 1.4 MPa), A case having a sealed internal space (pressure 1 atm) is formed.
(3) Put the battery packaging material in the above-mentioned case into an oven that can be depressurized, set the pressure in the oven to 0 atm, 140 to 160 ° C. at a temperature increase rate of 3 ° C./min. The temperature is heated to a set temperature T ° C. determined between and after reaching the set temperature T ° C., the set temperature T ° C. is maintained.

  The battery packaging material of the present invention has the above-described opening characteristics, and is gently opened by micro-cleavage at the time of opening. Therefore, when the temperature is raised to the set temperature T ° C., the packaging material does not reach until T ° C. is reached. It is used as a battery packaging material that is set so that the packaging material is opened quickly after reaching T ° C. without opening. The set temperature T determined by the battery is set between 140 and 160 ° C., and the set temperature differs depending on the type of battery to be packaged, usage, safety standards, and the like. For example, some batteries have a set temperature T set to 140 ° C., while others have a set temperature T set to 160 ° C. for safety standards. The battery packaging material of the present invention is provided as a packaging material having a sealing property and an opening property corresponding to a set temperature required by a battery to be applied. In addition, the time required for the battery to transition to the unsealed state after reaching T ° C. is determined within a range where safety can be ensured, and varies depending on the type and use of the battery, the rate of temperature increase, etc. Within 30 minutes, the battery packaging material of the present invention can satisfy the time.

  Furthermore, in the battery manufacturing process, minute foreign matters such as electrode active materials and electrode tab fragments may adhere to the surface of the sealant layer of the battery packaging material, which causes thin portions and through-holes in the sealant layer. May occur, and the insulation of the battery packaging material may be reduced. On the other hand, the battery packaging material of the present invention is formed from the resin composition containing the acid-modified polyolefin resin and the curing agent as described above, and has high heat resistance and mechanical properties when heat is applied during heat sealing. The insulating layer 4 is formed which has strength, high flexibility, and can suppress generation of fine cracks due to stress such as bending. For this reason, in the sealant layer 5, fine cracks that are likely to occur in thin portions, through holes due to foreign matters, voids due to foaming of the sealant layer that are generated when the sealant layer is heat sealed, and the like are formed. Even in this case, the insulating layer 4 can prevent the electrolytic solution from coming into direct contact with the metal layer, thereby protecting the metal layer 3. In addition, even when the sealant layer 5 bites foreign matter or the like, the insulating layer 4 having high heat resistance and high mechanical strength and flexibility can prevent deterioration of the insulating property of the battery packaging material due to foreign matter. Furthermore, in this invention, since the insulating layer 4 has high affinity with the metal layer 3 and the sealant layer 5, the adhesiveness between the insulating layer 4 and the metal layer 3 or the sealant layer 5 is high, and the durability is excellent.

  Specifically, the battery packaging material of the present invention can be used for sealing and housing battery elements such as a positive electrode, a negative electrode, and an electrolyte, and is provided with a space for housing the battery element. . The space is formed by press-molding a laminated sheet cut into a short shape.

  More specifically, a battery element including at least a positive electrode, a negative electrode, and an electrolyte is formed using the battery packaging material of the present invention with the metal terminals connected to each of the positive electrode and the negative electrode protruding outward. A battery using a battery packaging material is provided by covering the periphery of the element so that a flange portion (region where the sealant layers are in contact with each other) can be formed, and heat-sealing and sealing the sealant layers of the flange portion. Is done. In addition, when accommodating a battery element using the battery packaging material of the present invention, it is used so that the first sealant layer of the battery packaging material of the present invention is on the inner side (surface in contact with the battery element).

  The battery packaging material of the present invention may be used for either a primary battery or a secondary battery, but is preferably a secondary battery. The type of secondary battery to which the battery packaging material of the present invention is applied is not particularly limited. For example, a lithium ion battery, a lithium ion polymer battery, a lead battery, a nickel / hydrogen battery, a nickel / cadmium battery , Nickel / iron livestock batteries, nickel / zinc livestock batteries, silver oxide / zinc livestock batteries, metal-air batteries, polyvalent 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.

B. Method for Screening Resin Used for Insulating Layer and Sealant Layer The present invention further screens the resin used for the insulating layer and the sealant layer formed in the battery packaging material having the above-described sealing property and opening property. Provide a method.

Specifically, the screening method is a method of screening a resin used for an insulating layer and a sealant layer formed on a battery packaging material,
When the battery packaging material is heated up to a set temperature T ° C. determined between 140 ° C. and 160 ° C., the packaging material is not opened until the temperature reaches T ° C., and the packaging material quickly arrives after reaching T ° C. Used for batteries set to open,
The battery packaging material is composed of a laminate having a base layer, an adhesive layer, a metal layer, an insulating layer, and a sealant layer in this order, and the insulating layer is formed of a resin composition containing an acid-modified polyolefin resin and a curing agent. The sealant layer has a first sealant layer containing a polyolefin resin, and at least an acid-modified polyolefin resin is selected as a resin that forms an insulating layer, and at least a polyolefin resin is selected as a resin that forms a first sealant layer And the insulating layer and the first sealant layer have the following formulas (1) and (2):
(T-10) ≦ T _A ≦ (T-5) (1)
(T-5) ≦ T ₁ ≦ (T + 5) (2)
T _A : melting point of the insulating layer (° C.)
T ₁ : Melting point (° C.) of the first sealant layer
The resin for forming the insulating layer and the first sealant layer is selected so as to satisfy the above.

  The meaning of each term in the screening method is as described in the column “A. Battery packaging material”.

In the screening method of the present invention, when the sealant layer has the second sealant layer in addition to the first sealant layer, at least an acid-modified polyolefin resin is selected as the resin for forming the insulating layer, and the first sealant layer is formed. At least a polyolefin resin is selected as a resin to be used, at least one of an acid-modified polyolefin resin and a polyolefin resin is selected as a resin for forming the second sealant layer, and the insulating layer, the first sealant layer, and the second sealant layer are as follows: Formula (1)-(3)
(T-10) ≦ T _A ≦ (T-5) (1)
(T-5) ≦ T ₁ ≦ (T + 5) (2)
(T + 5) ≦ T ₂ ≦ (T + 10) (3)
T _A : melting point of the insulating layer (° C.)
T ₁ : Melting point (° C.) of the first sealant layer
T ₂ : Melting point (° C.) of the second sealant layer
The resin forming the insulating layer, the first sealant layer, and the second sealant layer is selected so as to satisfy the above.

  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.

Examples 1-6 and Comparative Examples 1-5
[Manufacture of battery packaging materials]
On the base material layer 1 made of a biaxially stretched nylon film (thickness 25 μm), a metal layer 3 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 polyol compound and an aromatic isocyanate compound) was applied to one surface of an aluminum foil to form an adhesive layer 2 (thickness 4 μm) on the metal layer 3. Next, after bonding the adhesive layer 2 and the base material layer 1 on the metal layer 3 under pressure and heating, an aging treatment is carried out at 40 ° C. for 24 hours, whereby base material layer 1 / adhesive layer 2 / metal layer 3 A laminate was obtained. In addition, the chemical conversion treatment of the aluminum foil used as the metal layer 3 is performed by rolling 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 applied to both surfaces of the aluminum foil and baked for 20 seconds under the condition that the film temperature was 180 ° C. or higher.

  Subsequently, in order to form the insulating layer 4 on the metal layer 3 side of the laminate, a resin composition containing an acid-modified polyolefin resin having a composition shown in Table 2 and a curing agent was applied to a thickness of 5 μm. , Dried. Next, the resin having the melting point shown in Table 2 for forming the first sealant layer 5a is extruded in a molten state from above the dried resin composition, whereby the first sealant layer 5a ( 30 μm thick) was laminated. Further, by heating the obtained laminate at 190 ° C. for 2 minutes, the laminate is obtained by sequentially laminating the base material layer 1 / adhesive layer 2 / metal layer 3 / insulating layer 4 / first sealant layer 5a. A packaging material was obtained. About melting | fusing point of resin which forms the insulating layer 4 and the 1st sealant layer 5a, it is the value measured by DSC method.

<Evaluation of sealing and unsealing properties of battery packaging materials>
Each battery packaging material obtained in Examples 1 to 6 and Comparative Examples 1 to 5 is cut into 80 mm × 150 mm, and then a 35 mm × 50 mm diameter mold (female mold) and a corresponding mold (Male type) was cold-molded at a depth of 3.0 mm at 0.4 MPa, and a recess was formed at the center. Regarding the battery packaging material after cold forming, it was visually observed whether or not pinholes were generated on the surface of the base material layer 1, and no pinholes were observed in any of the battery packaging materials. It was. Also, the two battery packaging materials after molding are stacked so that the sealant layers face each other, and the edge where the sealant layers overlap is heat sealed (175 ° C., 3 seconds, surface pressure 1.4 MPa). A case with a sealed internal space (pressure 1 atm) was formed. The battery packaging material thus made into a case is put in an oven that can be depressurized, and the pressure in the oven is set to 0 atm, and the temperature is raised to a set temperature T ° C. at a rate of 3 ° C./min. Then, T ° C was maintained for 30 minutes, and the state of the battery packaging material was visually confirmed at the time immediately before reaching T ° C and 30 minutes after reaching T ° C. In addition, this performance evaluation was performed by setting the set temperature T to three types of 140, 150, and 160 ° C. as described in Table 2.

  Based on the results observed in the test, the sealing and unsealing properties of each battery packaging material were evaluated according to the following criteria.

<Durability evaluation>
The battery packaging materials obtained in Examples 1 to 6 were each cut to 60 mm (MD direction, vertical direction) × 150 mm (TD direction, horizontal direction). Next, the cut battery packaging material is folded in half so that the sealant layers face each other in the TD direction, one side in the TD direction and one side in the MD direction are thermally welded, and one side in the TD direction is An open bag-shaped battery packaging material was prepared. The heat welding conditions were a temperature of 190 ° C., a surface pressure of 1.0 MPa, and a heating / pressurization time of 3 seconds. Next, 3 g of electrolytic solution was injected from the opening, and the opening was 7 mm wide and thermally welded under the same conditions as described above. The electrolytic solution was obtained by mixing lithium hexafluorophosphate with a solution mixed at a volume ratio of ethylene carbonate: diethyl carbonate: dimethyl carbonate = 1: 1: 1. Next, the part where the opening part of the packaging material for batteries was located was faced up, and it left still in an 85 degreeC thermostat for 24 hours.

  Next, each battery packaging material was taken out from the thermostatic layer, the battery packaging material was opened, and the electrolytic solution was taken out. Next, the folded portion of the battery packaging material was cut into a 15 mm wide strip to obtain a test piece. The first sealant layer 5a and the metal layer 3 of the obtained test piece were pulled at a rate of 50 mm / min using a tension machine (trade name AGS-50D manufactured by Shimadzu Corporation), and the peel strength (N / 15 mm) was measured (peel strength after durability test). On the other hand, the peel strength was measured in the same manner for the test pieces obtained by cutting the battery packaging materials obtained in Examples 1 to 6 into a width of 15 mm (peel strength before the durability test). The results are shown in Table 2.

<Insulation evaluation against foreign object biting>
The battery packaging materials obtained in Examples 1 to 6 were cut into a size of 40 mm in width and 100 mm in length to obtain test pieces. Next, the test piece was folded so that the short sides were opposed to each other, and arranged so that the surfaces of the first sealant layer 5a of the test piece were opposed to each other. Next, a wire of 25 μmφ was inserted between the surfaces of the first sealant layer 5a facing each other. Next, in this state, the sealant layers were heat-sealed with a heat-sealing machine composed of a flat plate-like hot plate having a width of 7 mm both in the vertical direction in the direction perpendicular to the length direction of the battery packaging material. Next, the terminals of the tester were connected to the surfaces of the base material layers on both sides so that the portion where the wire of the battery packaging material was sandwiched was in the center. Next, a voltage of 100 V was applied between the testers, and the time (seconds) until short-circuiting was measured. Three battery packaging materials obtained in Examples 1 to 6 (n = 3) each were measured for time (seconds) until they were short-circuited, and all three were 10 seconds or longer. Those with less than 2 seconds were marked with x. The results are shown in Table 2.

<Insulation evaluation against cracks>
The battery packaging materials obtained in Examples 1 to 6 were cut into sheet pieces of 60 mm (MD direction) × 60 mm (TD direction, lateral direction). Next, these sheet pieces were folded in two in the MD direction (longitudinal direction), and two opposite sides were heat-sealed with a width of 7 mm to produce 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 insulation evaluation test with respect to a crack was implemented using the impulse application system (Nippon Technate make, a lithium ion battery insulation tester). About Examples 1-6, the said lithium ion battery is prepared 5 each, the impulse voltage of the applied voltage 100V is applied between the negative electrode terminal and aluminum foil of each lithium ion battery, and the voltage drop after 99 msec is shown. When there was no voltage drop in all five, it was marked with ◯. The results are shown in Table 2.

In the packaging material for a battery in sequence and a first sealant layer 5a including an insulating layer and a polyolefin resin formed of a resin composition containing an acid-modified polyolefin resin and a curing agent, the set temperature T and the melting point T _A of the insulating layer The difference (T _A −T) is −10 ° C. or more and −5 ° C. or less, and the difference (T ₁ −T) between the melting point T ₁ of the first sealant layer 5a and the set temperature T is −5 ° C. or more and + 5 ° C. In Examples 1 to 6 satisfying the following, at least a part of the insulating layer 4 was peeled off from the interface of the metal layer 3 until the set temperature T ° C., but the insulating layer 4 and the first sealant layer 5a became bag-like. 30 minutes after reaching the set temperature T.degree. C. while maintaining the internal sealing state, a minute crack such as a pinhole occurs in the insulating layer 4 and the first sealant layer 5a separated from the metal layer 3. Can lead to opening It was. In contrast, in Comparative Examples 1 to 6 where the difference (T ₁ −T) between the melting point T ₁ of the first sealant layer 5a and the set temperature T does not satisfy −5 ° C. or more and + 5 ° C. or less, the set temperature T ° C. Before reaching the temperature, the heat seal part was agglomerated and the sealant layer was broken or the sealant layer could not be opened even after 30 minutes at the set temperature T ° C.

  On the other hand, in the battery packaging materials of Examples 1 to 6 including an insulating layer formed of a resin composition containing an acid-modified polyolefin resin and a curing agent, the insulation against both foreign matter biting and cracking is high and durable. The change in peel strength before and after the property test was small and the durability was excellent.

Examples 7-15 and Comparative Examples 6-12
[Manufacture of battery packaging materials]
In the same manner as in Example 1, a laminate of base material layer 1 / adhesive layer 2 / metal layer 3 was prepared. Next, in order to form an insulating layer on the metal layer 3 side of the laminate, a resin composition containing a modified polyolefin resin having a composition shown in Table 3 and a curing agent was applied to a thickness of 5 μm and dried. I let you. Next, in Examples 7, 8, 10, 13 to 15 and Comparative Examples 6 to 12, a resin for forming the second sealant layer 5b and a resin for forming the first sealant layer are formed on the dried resin composition. Were coextruded in a molten state, thereby laminating a second sealant layer (thickness 20 μm) and a first sealant layer 5a (thickness 10 μm) on the insulating layer. Further, the obtained laminate was heated at 190 ° C. for 2 minutes, whereby base layer 1 / adhesive layer 2 / metal layer 3 / insulating layer 4 / second sealant layer 5b / first sealant layer 5a were sequentially laminated. A battery packaging material comprising a laminate was obtained.

  On the other hand, in Example 9, a resin for forming the second sealant layer 5b (thickness: 10 μm) is applied on the dried resin composition of the insulating layer and dried, and then the first sealant layer 5a is formed. The resin to be melt-extruded is made into a single film, and this is overlaid on the second sealant layer 5b and pressure-bonded at 160 ° C., and then heated in an oven at 190 ° C. for 2 minutes, whereby the second sealant layer 5b From the laminate in which the first sealant (thickness 20 μm) is laminated thereon and the base material layer 1 / adhesive layer 2 / metal layer 3 / insulating layer 4 / second sealant layer 5b / first sealant layer 5a are laminated in this order. A battery packaging material was obtained.

  Further, in Example 11, a resin for forming the second sealant layer 5b is applied from above the dried resin composition of the insulating layer and dried, and then the resin for forming the first sealant layer 5a is melt-extruded. Then, a single film was prepared, and this was overlaid on the second sealant layer 5b, pressure-bonded at 160 ° C., and then heated in an oven at 190 ° C. for 2 minutes, whereby the first sealant layer was formed on the second sealant layer 5b. A packaging material for a battery comprising a laminate in which a base layer 1 / adhesive layer 2 / metal layer 3 / insulating layer 4 / second sealant layer 5b / first sealant layer 5a are sequentially laminated. Got.

  Further, in Example 12, the third sealant layer 5c (thickness 5 μm) / second sealant layer 5b (thickness 20 μm) formed of the resin shown in Table 3 from above the dried resin composition of the insulating layer. ) / Laminated films of the first sealant layer 5a (thickness 5 μm) were laminated and laminated by heat lamination. Furthermore, by heating the obtained laminate at 190 ° C. for 2 minutes, material layer 1 / adhesive layer 2 / metal layer 3 / insulating layer 4 / third sealant layer 5c / second sealant layer 5b / first sealant layer 5a The battery packaging material which consists of a laminated body laminated | stacked in order was obtained. The resin, the curing agent, and the like that form the insulating layer 4, the first sealant layer 5a, the second sealant layer 5b, and the third sealant layer 5c are as shown in Table 3. Further, the melting points of the resins forming the insulating layer 4, the first sealant layer 5a, the second sealant layer 5b, and the third sealant layer 5c are values measured by the DSC method.

<Evaluation of sealing and unsealing properties of battery packaging materials>
In the same manner as in Example 1, the battery packaging materials obtained in Examples 7 to 15 and Comparative Examples 6 to 12 were evaluated for sealability and openability. The results are shown in Table 3.

<Durability evaluation>
In the same manner as in Example 1, the battery packaging materials obtained in Examples 7 to 13 were evaluated for durability. The results are shown in Table 3.

<Insulation evaluation against foreign object biting>
In the same manner as in Example 1, the battery packaging materials obtained in Examples 7 to 13 were evaluated for insulation against foreign object biting. The results are shown in Table 3.

<Insulation evaluation against cracks>
In the same manner as in Example 1, the battery packaging materials obtained in Examples 7 to 13 were evaluated for insulation against cracks. The results are shown in Table 3.

A battery comprising an insulating layer formed of a resin composition containing an acid-modified polyolefin resin and a curing agent, a second sealant layer 5b containing a polyolefin resin or an acid-modified polyolefin resin, and a first sealant layer 5a containing a polyolefin resin in this order. In the packaging material, the difference (T _A −T) between the melting point T _A of the insulating layer and the set temperature T is −10 ° C. or more and −5 ° C. or less, and the melting point T ₂ and the set temperature T of the second sealant layer 5b Difference (T ₂ −T) is −10 ° C. to −5 ° C., and the difference (T ₁ −T) between the melting point T ₁ of the first sealant layer 5a and the set temperature T is −5 ° C. to + 5 ° C. In Examples 7 to 15 satisfying all of the above, at least a part of the insulating layer 4 was peeled off from the interface of the metal layer 3 until the set temperature T ° C was reached, but the insulating layer 4 and the sealant layer 5 were formed into a bag shape inside. While maintaining the sealed state of After 30 minutes from the constant temperature T ° C. reached resulting fine cleavage, such as a pin hole in the insulating layer 4 and the sealant layer 5 of the release portion from the metal layer 3, it had been able to lead to opening under mild conditions. On the other hand, in Comparative Examples 6 to 12 where the difference (T ₁ −T) between the melting point T ₁ of the first sealant layer 5a and the set temperature T does not satisfy −5 ° C. or more and + 5 ° C. or less, the set temperature T ° C. Before reaching the temperature, the heat seal portion was broken and the sealant layer 5 was broken, or even after 30 minutes had reached the set temperature T ° C., the seal could not be opened.

  On the other hand, in the battery packaging materials of Examples 7 to 13 provided with an insulating layer formed of a resin composition containing an acid-modified polyolefin resin and a curing agent, the insulation against both foreign matter biting and cracking is high and durable. The change in peel strength before and after the property test was small and the durability was excellent.

Examples 16 to 31 and Comparative Examples 13 to 15
[Manufacture of battery packaging materials]
In the same manner as in Example 1, a laminate of base material layer 1 / adhesive layer 2 / metal layer 3 was prepared. Next, in order to form an insulating layer on the metal layer 3 side of the laminate, a resin composition containing a modified polyolefin resin and a curing agent each having the composition shown in Table 4 was applied to a thickness of 5 μm and dried. It was. Next, the second sealant layer is formed on the insulating layer by co-extruding the resin forming the second sealant layer 5b and the resin forming the first sealant layer 5a in a molten state from above the dried resin composition. 5b (thickness 20 μm) and the first sealant layer 5a (thickness 10 μm) were laminated. Furthermore, by heating the obtained laminate by the following heating methods A to D, the base material layer 1 / adhesive layer 2 / metal layer 3 / insulating layer 4 / second sealant layer 5b / first sealant layer 5a are obtained. A battery packaging material comprising a laminate laminated in order was obtained.
<Heating method>
A: Heat at 190 ° C. for 2 minutes B: Heat at 190 ° C. for 2 minutes and then age at 60 ° C. for 1 day C: After aging at 60 ° C. for 1 day, heat at 190 ° C. for 2 minutes D: At 80 ° C. The resin, the curing agent, and the like that form the insulating layer 4, the first sealant layer 5a, and the second sealant layer 5b are as shown in Table 4. Further, the melting points of the resins forming the insulating layer 4, the first sealant layer 5a, and the second sealant layer 5b are values measured by the DSC method.

<Evaluation of sealing and unsealing properties of battery packaging materials>
In the same manner as in Example 1, the battery packaging materials obtained in Examples 16 to 31 and Comparative Examples 13 to 15 were evaluated for sealability and openability. The results are shown in Table 4.

<Durability evaluation>
In the same manner as in Example 1, the battery packaging materials obtained in Examples 16 to 31 and Comparative Examples 13 to 15 were evaluated for durability. The results are shown in Table 4.

<Insulation evaluation against foreign object biting>
In the same manner as in Example 1, the battery packaging materials obtained in Examples 16 to 31 and Comparative Examples 13 to 15 were evaluated for insulation against foreign object biting. The results are shown in Table 4.

<Insulation evaluation against cracks>
In the same manner as in Example 1, the battery packaging materials obtained in Examples 16 to 31 and Comparative Examples 13 to 15 were evaluated for insulation against cracks. The results are shown in Table 4.

A battery comprising an insulating layer formed of a resin composition containing an acid-modified polyolefin resin and a curing agent, a second sealant layer 5b containing a polyolefin resin or an acid-modified polyolefin resin, and a first sealant layer 5a containing a polyolefin resin in this order. In the packaging material, the difference (T _A −T) between the melting point T _A of the insulating layer and the set temperature T is −10 ° C. or more and −5 ° C. or less, and the melting point T ₂ and the set temperature T of the second sealant layer 5b Difference (T ₂ −T) is −10 ° C. to −5 ° C., and the difference (T ₁ −T) between the melting point T ₁ of the first sealant layer 5a and the set temperature T is −5 ° C. to + 5 ° C. In Examples 16 to 31 and Comparative Examples 13 to 15 that satisfy all of the conditions, at least part of the insulating layer 4 was peeled off from the interface of the metal layer 3 until the set temperature T ° C. was reached, but the sealant layer 5 became a bag shape. Sealed inside 30 minutes after reaching the set temperature T.degree. C., the insulating layer 4 and the sealant layer 5 separated from the metal layer 3 are finely cleaved like a pinhole, leading to opening in a gentle state. It was done.

  On the other hand, in the battery packaging materials of Examples 16 to 31 including the insulating layer 4 formed of a resin composition containing an acid-modified polyolefin resin and a curing agent, the insulation against both foreign matter biting and cracking is high and durable. The change in peel strength before and after the property test was small and the durability was excellent. On the other hand, in the battery packaging material of Comparative Example 13 in which the resin composition forming the insulating layer 4 did not contain a curing agent, the insulation against foreign object biting was low and the durability was also low. Further, in the battery packaging materials of Comparative Examples 14 and 15 in which the resin composition forming the insulating layer did not contain a curing agent, the insulation against both foreign matter biting and cracking was low, and the durability was also low.

DESCRIPTION OF SYMBOLS 1 Base material layer 2 Adhesion layer 3 Metal layer 4 Insulation layer 5 Sealant layer 5a First sealant layer 5b Second sealant layer 5c Third sealant layer 10 Fine cleavage

Claims (12)

When the temperature is raised to a set temperature T ° C determined between 140 ° C and 160 ° C, the packaging material is not opened until the temperature reaches T ° C. After reaching T ° C, the packaging material is opened quickly. A battery packaging material used for a battery,
It consists of a laminate having at least a base material layer, an adhesive layer, a metal layer, an insulating layer, and a sealant layer in this order,
The insulating layer is formed of a resin composition containing an acid-modified polyolefin resin and a curing agent,
The sealant layer has a first sealant layer containing a polyolefin resin,
The insulating layer and the first sealant layer are represented by the following formulas (1) and (2):
−10 ≦ T _A −T ≦ −5 (1)
−5 ≦ T ₁ −T ≦ 5 (2)
T _A : melting point (° C.) of the insulating layer
T ₁ : Melting point (° C.) of the first sealant layer
Battery packaging material that satisfies this relationship.   The acid-modified polyolefin resin in the insulating layer was modified with an acid-modified polyolefin resin modified with an unsaturated carboxylic acid or an acid anhydride thereof, and an unsaturated carboxylic acid or acid anhydride and a (meth) acrylic acid ester. The battery packaging material according to claim 1, which is at least one of acid-modified polyolefin resins.   The acid-modified polyolefin resin modified with the unsaturated carboxylic acid or acid anhydride thereof is formed by modifying at least one of a polyethylene resin or a polypropylene resin with the unsaturated carboxylic acid or acid anhydride thereof. The battery packaging material according to claim 2, wherein   The acid-modified polyolefin resin modified with the unsaturated carboxylic acid or acid anhydride thereof and a (meth) acrylic acid ester is such that at least one of a polyethylene resin and a polypropylene resin is the unsaturated carboxylic acid or acid anhydride thereof. The battery packaging material according to claim 2, which is modified with and (meth) acrylic acid ester.   The battery packaging material according to any one of claims 1 to 4, wherein the polyolefin resin contained in the first sealant layer contains at least propylene as a constituent monomer.   The battery packaging material according to claim 1, wherein the insulating layer has a thickness of 0.1 to 20 μm, and the first sealant layer has a thickness of 1 to 40 μm.   The battery packaging material according to any one of claims 1 to 6, wherein the metal layer is an aluminum foil.   The said hardening | curing agent is a packaging material for batteries in any one of Claims 1-7 containing at least 1 sort (s) selected from the group which consists of a polyfunctional isocyanate compound, a carbodiimide compound, an epoxy compound, and an oxazoline compound.   The said resin composition WHEREIN: Content of the said hardening | curing agent exists in the range of 0.1 mass part-50 mass parts with respect to 100 mass parts of said acid-modified polyolefin resin, The any one of Claims 1-8. Battery packaging material. The sealant layer further includes a second sealant layer including at least one of an acid-modified polyolefin resin and a polyolefin resin between the insulating layer and the first sealant layer, and the second sealant layer is represented by the following formula (3 )
5 ≦ T ₂ −T ≦ 10 (3)
T ₂ : Melting point (° C.) of the second sealant layer
The battery packaging material according to claim 1, wherein   The battery packaging material according to claim 10, wherein the acid-modified polyolefin resin and the polyolefin resin in the second sealant layer contain at least propylene as a constituent monomer.   The battery by which the battery element provided with the positive electrode, the negative electrode, and the electrolyte at least is accommodated in the battery packaging material in any one of Claims 1-11.