JP2015146315A - Packaging material for batteries - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a film-shaped packaging material for batteries which allows a thinner film formation to be materialized by providing a coating layer as a top layer instead of an adhesion layer and a base material layer in a conventional film-shaped packaging material for batteries, and which is high in the film strength of the coating layer and superior in formability, and enables the shortening of a lead time.SOLUTION: A packaging material for batteries comprises a laminate having at least, a coating layer, a barrier layer, and sealant layer in this order. The coating layer is composed of a monolayer or multilayer formed by a hardened material of a resin composition including a thermosetting resin and a hardening accelerator. The resin composition used to form at least one layer of the coating layer is arranged to include reactive resin beads, which enables the rise in formability, and the shortening of a lead time.

Description

  The present invention is a film-like battery packaging material that is thinned by providing a coating layer on the barrier layer as the outermost layer, and has excellent moldability and can also shorten the lead time. About.

  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 frequently used as battery packaging.

  On the other hand, as the performance of electric vehicles, hybrid electric vehicles, personal computers, cameras, mobile phones, and the like increases, the batteries are required to have various shapes, as well as to be thinner and lighter. 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, a film-like laminate in which a base material layer / adhesive layer / barrier layer / sealant layer are sequentially laminated is proposed as a battery packaging material that can be easily processed into various shapes and can be made thinner and lighter. (For example, refer to 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, in recent years, there has been an increasing demand for smaller and thinner batteries, and further thinning of film-like battery packaging materials is required to follow the demand. As a method for thinning the whole film packaging material for a battery, there is a method of thinning a base material layer in which a resin film having a thickness of about 10 to 20 μm is used. However, there is a problem in that the reduction in the thickness of the resin film has a manufacturing limit, and the manufacturing cost of the battery packaging material increases due to the processing cost required to reduce the thickness of the resin film.

  In addition, the coating layer formed by coating the thermosetting resin compared to the resin film can greatly reduce the film thickness. It is also effective to replace the adhesive layer and the base material layer laminated on each other with a coating layer formed of a thermosetting resin.

  However, in film-like battery packaging materials, when a coating layer is formed with a thermosetting resin instead of an adhesive layer and a base material layer, aging under high temperature conditions is performed for several days to several weeks in the curing process. Therefore, there is a problem in that the lead time is prolonged, and the product defect is caused by being exposed to high temperature conditions and temperature changes for a long time.

  In recent years, there has been no need for further improvement in battery performance, and accordingly, an increase in battery capacity has been demanded. Film-like battery packaging materials are processed into a predetermined shape by deep drawing or the like to seal the battery element, so the battery capacity is increased by improving the moldability of film-like battery packaging materials. To increase the molding depth (elongation during molding).

  With such a conventional technology as a background, it is possible to improve the moldability and lead time of film-like battery packaging materials that have been made thinner by providing a coating layer instead of an adhesive layer and a base material layer. Development of technology is allowed.

JP 2001-202927 A

  The present invention is a film-like battery packaging material that can realize thinning by providing a coating layer as the outermost layer in place of the adhesive layer and the base material layer in the conventional film-like battery packaging material, It is an object of the present invention to provide a film-like battery packaging material that has moldability and can shorten the lead time.

  The inventors of the present invention have conducted intensive studies to solve the above problems, and at least in a battery packaging material comprising a laminate having in this order a coating having a coating layer, a barrier layer, and a sealant layer in this order, The coating layer is set to a single layer or a multilayer structure formed of a cured product of a resin composition containing a thermosetting resin and a curing accelerator, and is used for forming at least one layer of the coating layer. It has been found that by incorporating reactive resin beads into the resin composition, it is possible to improve moldability and shorten lead time. Furthermore, in the battery packaging material having the above-described configuration, by including a pigment and / or dye in at least one layer of the coating layer, the battery packaging material can be given distinctiveness, and the thermal conductivity can be increased. It has been found that the heat dissipation can be improved. The present invention has been completed by further studies based on such knowledge.

That is, this invention provides the invention of the aspect hung up below.
Item 1. It consists of a laminate having at least a coating layer, a barrier layer, and a sealant layer in this order,
The coating layer is composed of a single layer or a multilayer structure formed of a cured product of a resin composition containing a thermosetting resin and a curing accelerator,
Reactive resin beads are included in the resin composition used to form at least one layer of the coating layer.
A battery packaging material characterized by the above.
Item 2. The coating layer has a three-layer structure in which a first coating layer, a second coating layer, and a third coating layer are arranged in this order from the outermost surface side to the barrier layer side, and the formation of the second coating layer Item 4. The battery packaging material according to Item 1, wherein the reactive resin beads are included in the resin composition used in the battery.
Item 3. Item 3. The battery packaging material according to Item 1 or 2, wherein the reactive resin beads are urethane resin beads or acrylic resin beads having a functional group.
Item 4. Item 4. The battery packaging material according to any one of Items 1 to 3, wherein the reactive resin beads have a refractive index of 1.3 to 1.8.
Item 5. Item 5. The battery packaging material according to any one of Items 1 to 4, wherein the resin composition used for forming at least one layer of the coating layer contains a pigment and / or a dye.
Item 6. Item 6. The battery packaging material according to Item 5, wherein the resin composition used for forming at least one layer of the coating layer contains an inorganic pigment.
Item 7. Any one of Items 1 to 6, wherein the thermosetting resin is at least one selected from the group consisting of an epoxy resin, an amino resin, an acrylic resin, a urethane resin, a phenol resin, an unsaturated polyester resin, and an alkyd resin. A packaging material for a battery as described in 1.
Item 8. Item 1-7, wherein the curing accelerator is at least one selected from the group consisting of an amidine compound, a carbodiimide compound, a ketimine compound, a hydrazine compound, a sulfonium salt, a benzothiazolium salt, and a tertiary amine compound. The battery packaging material according to any one of the above.
Item 9. Item 9. The battery packaging material according to any one of Items 1 to 8, wherein the barrier layer is a metal foil.
Item 10. Item 10. The battery packaging material according to any one of Items 1 to 9, wherein the entire battery packaging material has a thickness of 40 to 120 μm.
Item 11. A coating layer forming step of applying a resin composition containing a thermosetting resin and a curing accelerator on the barrier layer, and curing by heating;
The coating layer forming step is performed once or a plurality of times, and at least once in the coating layer forming step, the resin composition containing reactive resin beads is used,
Before or after the coating layer forming step, a sealant layer is laminated on the surface of the barrier layer opposite to the surface on which the coating layer is laminated.
A method for producing a packaging material for a battery.
Item 12. Item 11. 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 10.

  The battery packaging material of the present invention is composed of a laminate having at least a coating layer, a barrier layer, and a sealant layer in this order, and an adhesive layer is formed on the barrier layer like a conventional film-shaped battery packaging material. Since the base material layer is not provided, the film thickness can be reduced, and the battery can be reduced in size and thickness.

  In addition, the battery packaging material of the present invention, in the at least one layer constituting the coating layer provided on the barrier layer, the reactive resin beads are present in a state of being chemically bonded to the thermosetting resin, Excellent moldability can be provided, and cracks, pinholes, and the like can be prevented from occurring even if the molding depth during deep drawing is increased.

  Furthermore, in the battery packaging material of the present invention, each layer constituting the coating layer provided on the barrier layer is formed by a cured product of a resin composition containing a thermosetting resin and a curing accelerator. In the curing process of the coating layer, it can be cured in a short time without requiring aging under high temperature conditions, so the lead time can be shortened, and further, the occurrence of product defects due to long-term exposure to high temperature conditions can be prevented. You can also.

  Moreover, in the conventional film-shaped battery packaging material, when providing distinctiveness by color tone for each type of battery, it is necessary to add a pigment and / or dye to either the adhesive layer or the base material layer. However, when a pigment and / or dye is added to the adhesive layer, the adhesive strength of the adhesive layer is reduced, and when a pigment and / or dye is added to the base layer, the manufacturing cost of the base layer is increased. There was a drawback of inviting. On the other hand, in the battery packaging material of the present invention, since the battery packaging material can be given distinctiveness by including a pigment and / or dye in at least one layer constituting the coating layer, the conventional film-like material is used. It is also possible to overcome the disadvantages of imparting distinguishability to the battery packaging material. Furthermore, when a pigment and / or dye (particularly inorganic pigment) is contained in at least one layer constituting the coating layer, the thermal conductivity of the battery packaging material can be increased and the heat dissipation can be improved. It can also contribute to the improvement of safety.

It is a figure which shows an example of the cross-section of the packaging material for batteries of this invention. It is a figure which shows an example of the cross-section of the packaging material for batteries of this invention.

  The battery packaging material of the present invention comprises a laminate having at least a coating layer, a barrier layer, and a sealant layer in this order, and the coating layer is a cured resin composition containing a thermosetting resin and a curing accelerator. A reactive resin bead is included in the resin composition which is composed of a single layer or a multi-layer structure formed of a material and is used for forming at least one layer of the coating layer. Hereinafter, the battery packaging material of the present invention will be described in detail.

1. Laminated Structure of Battery Packaging Material As shown in FIG. 1, the battery packaging material of the present invention has a laminated structure composed of a laminate having at least a coating layer 1, a barrier layer 2, and a sealant layer 3 in this order. In the battery packaging material of the present invention, the coating layer 1 may be a single layer or a multilayer composed of two or more layers.

  The coating layer 1 is preferably a multilayer composed of two or more layers, more preferably a multilayer composed of two or three layers in order to provide a thick film capable of providing sufficient insulation. Particularly preferred is a multilayer composed of three layers. FIG. 2 shows a case where the coating layer 1 has a three-layer structure having a first coating layer 1a, a second coating layer 1b, and a third coating layer 1c in this order from the outermost surface toward the barrier layer 2 side. The laminated structure of the battery packaging material of invention is shown.

  In the battery packaging material of the present invention, the coating layer 1 is the outermost surface layer, and the sealant layer 3 is the innermost layer. That is, when the battery is assembled, the sealant layers 3 positioned at the periphery of the battery element are thermally welded to seal the battery element, thereby sealing the battery element.

  Moreover, in the battery packaging material of the present invention, an adhesive layer 4 may be provided between the barrier layer 2 and the sealant layer 3 as necessary for the purpose of enhancing the adhesion.

2. Composition of each layer forming battery packaging material [Coating layer 1]
In the battery packaging material of the present invention, the coating layer 1 is a layer that is provided on the barrier layer 2 and forms the outermost layer of the battery packaging material. Further, the coating layer 1 is composed of a single layer or a multilayer structure formed of a cured product of a resin composition containing a thermosetting resin and a curing accelerator, and at least one layer (cured) constituting the coating layer. Reactive resin beads are included in the resin composition for forming the product.

(Thermosetting resin)
The resin composition used for forming the coating layer 1 contains a thermosetting resin. Any thermosetting resin may be used as long as it causes polymerization upon heating to form a polymer network structure and cure. Although it does not restrict | limit especially as a thermosetting resin used for formation of the coating layer 1, Specifically, an epoxy resin, an amino resin (melamine resin, a benzoguanamine resin, etc.), an acrylic resin, a urethane resin, a phenol resin, non-resin Examples thereof include saturated polyester resins and alkyd resins. These thermosetting resins may be used individually by 1 type, and may be used in combination of 2 or more type.

  Among these thermosetting resins, from the viewpoints of further shortening the curing time of the coating layer 1 and further improving the film strength and moldability, preferably a urethane resin, an epoxy resin, and more preferably a two-part curable resin. A urethane resin, a two-component curable epoxy resin, particularly preferably a two-component curable urethane resin.

  Specific examples of the two-component curable urethane resin include a combination of a polyol compound (main agent) and an isocyanate compound (curing agent). As the two-component curable epoxy resin, specifically, an epoxy resin (main agent) and , Acid anhydrides, amine compounds, or combinations of amino resins (curing agents).

  In the two-component curable urethane resin, the polyol compound used as the main agent is not particularly limited, and examples thereof include polyester polyol, polyester polyurethane polyol, polyether polyol, and polyether polyurethane polyol. These polyol compounds may be used individually by 1 type, and may be used in combination of 2 or more type.

  In the two-part curable urethane resin, the isocyanate compound used as a curing agent is not particularly limited. For example, polyisocyanate, its adduct, its isocyanurate-modified, its carbodiimide-modified, and its allophanate. A modified body, its burette modified body, etc. are mentioned. Specific examples of the polyisocyanate include diphenylmethane diisocyanate (MDI), polyphenylmethane diisocyanate (polymeric MDI), toluene diisocyanate (TDI), hexamethylene diisocyanate (HDI), and bis (4-isocyanatocyclohexyl) methane (H12MDI). , Aromatic diisocyanates such as isophorone diisocyanate (IPDI), 1,5-naphthalene diisocyanate (1,5-NDI), 3,3′-dimethyl-4,4′-diphenylene diisocyanate (TODI), xylene diisocyanate (XDI) Aliphatic diisocyanates such as tramethylene diisocyanate, hexamethylene diisocyanate, trimethylhexamethylene diisocyanate, isophorone diisocyanate DOO; 4,4'-methylenebis (cyclohexyl isocyanate), alicyclic diisocyanates such as isophorone diisocyanate; 1,5-naphthalene diisocyanate (1, 5-NDI) polycyclic aromatic diisocyanates such as are exemplified. Specific examples of the adduct include those obtained by adding trimethylolpropane, glycol and the like to the polyisocyanate. These isocyanate compounds may be used individually by 1 type, and may be used in combination of 2 or more type.

  In the case of the coating layer 1 having a single layer structure or the layer located on the outermost layer of the coating layer 1 having a multilayer structure, the thermosetting resin has a polycyclic aromatic skeleton and / or a heterocyclic skeleton Can be used to provide even better chemical resistance. Specific examples of the thermosetting resin having a polycyclic aromatic skeleton include an epoxy resin having a polycyclic aromatic skeleton and a urethane resin having a polycyclic aromatic skeleton. Examples of the thermosetting resin having a heterocyclic skeleton include amino resins such as melamine resin and benzoguanamine resin. These thermosetting resins having a polycyclic aromatic skeleton and / or a heterocyclic skeleton may be either a one-component curable type or a two-component curable type.

  More specifically, as an epoxy resin having a polycyclic aromatic skeleton, a reaction product of dihydroxynaphthalene and epihalohydrin; a condensate of naphthol and aldehydes (naphthol novolak resin) and a reaction product of epihalohydrin; dihydroxy Condensate of naphthalene and aldehydes and reaction product of epihalohydrin; condensate of mono or dihydroxynaphthalene and xylylene glycol and reaction product of epihalohydrin; adduct of mono or dihydroxynaphthalene and diene compound, and epihalohydrin A reaction product of polynaphthols in which naphthols are directly coupled with epihalohydrin, and the like.

  More specifically, examples of the urethane resin having a polycyclic aromatic skeleton include a reaction product of a polyol compound and an isocyanate compound having a polycyclic aromatic skeleton.

(Curing accelerator)
The resin composition used for forming the coating layer 1 contains a curing accelerator. Thus, by coexisting a curing accelerator together with a thermosetting resin, the coating layer can be cured in a short time without requiring aging under high temperature conditions during production, and the lead time can be shortened. .

  Here, the “curing accelerator” is a substance that does not form a crosslinked structure by itself, but promotes a crosslinking reaction of a thermosetting resin, and has an action of promoting a crosslinking reaction of a thermosetting resin. Is also a substance that may form a crosslinked structure.

  The type of curing accelerator is appropriately selected according to the thermosetting resin to be used so that the hardness described above can be satisfied. For example, an amidine compound, a carbodiimide compound, a ketimine compound, a hydrazine compound, a sulfonium salt, a benzoic acid Examples include thiazolium salts and tertiary amine compounds.

  The amidine compound is not particularly limited, and examples thereof include imidazole compounds, 1,8-diazabicyclo [5.4.0] undec-7ene (DBU), 1,5-diazabicyclo [4.3.0] none. 5-ene (DBN), a guanidine compound, etc. are mentioned. Specific examples of the imidazole compound include 2-methylimidazole, 2-ethylimidazole, 2-undecylimidazole, 2,4-dimethylimidazole, 2-heptadecylimidazole, 1,2-dimethylimidazole, 1,2 -Diethylimidazole, 2-ethyl-4-methylimidazole, 2-phenylimidazole, 1-benzyl-2-phenylimidazole, 1-cyanoethyl-2-methylimidazole, 1-cyanoethyl-2-undecylimidazole, 1-benzyl- 2-methylimidazole, 2,4-diamino-6- [2′-methylimidazolyl- (1) ′]-ethyl-S-triazine, 2,4-diamino-6- [2′-ethyl-4′-methyl Imidazolyl- (1) ′]-ethyl-S-triazine, 2,4-diamino- -[2'-undecylimidazolyl] -ethyl-S-triazine, 2,4-diamino-6- [2'-methylimidazolyl- (1) ']-ethyl-S-triazine isocyanurate oxidation adduct, 2- Examples include phenyl-4-methyl-5-hydroxymethylimidazole, 2-phenyl-4,5-dihydroxymethylimidazole, 2-aryl-4,5-diphenylimidazole and the like. These amidine compounds may be used individually by 1 type, and may be used in combination of 2 or more type.

  The carbodiimide compound is not particularly limited. For example, N, N′-dicyclohexylcarbodiimide, N, N′-diisopropylcarbodiimide, 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide, N- [3- ( Dimethylamino) propyl] -N'-ethylcarbodiimide, N- [3- (dimethylamino) propyl] -N'-ethylcarbodiimide methiodide, N-tert-butyl-N'-ethylcarbodiimide, N-cyclohexyl-N Examples include '-(2-morpholinoethyl) carbodiimide meso-p-toluenesulfonate, N, N'-di-tert-butylcarbodiimide, N, N'-di-p-tolylcarbodiimide, and the like. These carbodiimide compounds may be used individually by 1 type, and may be used in combination of 2 or more type.

  The ketimine compound is not particularly limited as long as it has a ketimine bond (N = C), and examples thereof include a ketimine compound obtained by reacting a ketone with an amine. Specific examples of the ketone include methyl ethyl ketone, methyl isopropyl ketone, methyl tertiary butyl ketone, methyl cyclohexyl ketone, diethyl ketone, ethyl propyl ketone, ethyl butyl ketone, dipropyl ketone, dibutyl ketone, and diisobutyl ketone. Specific examples of the amine include o-phenylenediamine, m-phenylenediamine, p-phenylenediamine, m-xylylenediamine, diaminodiphenylmethane, diaminodiphenylsulfone, and diaminodiethyldiphenylmethane; ethylenediamine , Propylenediamine, butylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, hexamethylenediamine, trimethylhexamethylenediamine, 1,2-propanediamine, iminobispropylamine, methyliminobispropylamine, etc. Aliphatic polyamines; N-aminoethylpiperazine, 3-butoxyisopropylamine and the like monoamines and polyesters having an ether bond in the main chain Terpone diamines; cyclophoric amines such as isophorone diamine, 1,3-bisaminomethylcyclohexane, 1-cyclohexylamino-3-aminopropane, 3-aminomethyl-3,3,5-trimethylcyclohexylamine: norbornane skeleton Polyamide amine having an amino group at the molecular end of polyamide; 2,5-dimethyl-2,5-hexamethylenediamine, mensendiamine, 1,4-bis (2-amino-2-methylpropyl) piperazine, etc. Is given as a specific example. These ketimine compounds may be used individually by 1 type, and may be used in combination of 2 or more type.

  The hydrazine compound is not particularly limited, and examples thereof include dipic acid dihydrazide and isophthalic acid dihydrazide. These hydrazine compounds may be used individually by 1 type, and may be used in combination of 2 or more type.

  The sulfonium salt is not particularly limited. For example, 4-acetophenyldimethylsulfonium hexafluoroantimonate, 4-acetophenyldimethylsulfonium hexafluoroarsenate, dimethyl-4- (benzyloxycarbonyloxy) phenylsulfonium hexafluoroantimony , Alkylsulfonium salts such as dimethyl-4- (benzoyloxy) phenylsulfonium hexafluoroantimonate, dimethyl-4- (benzoyloxy) phenylsulfonium hexafluoroarsenate; benzyl-4-hydroxyphenylmethylsulfonium hexafluoroantimonate, 4-acetoxyphenylbenzylmethylsulfonium hexafluoroantimonate, benzyl-4-methoxypheny Benzylsulfonium salts such as methylsulfonium hexafluoroantimonate, benzyl-3-chloro-4-hydroxyphenylmethylsulfonium hexafluoroarsenate, 4-methoxybenzyl-4-hydroxyphenylmethylsulfonium hexafluorophosphate; dibenzyl-4-hydroxyphenyl Dibenzylsulfonium such as sulfonium hexafluoroantimonate, dibenzyl-4-hydroxyphenylsulfonium hexafluorophosphate, dibenzyl-4-methoxyphenylsulfonium hexafluoroantimonate, benzyl-4-methoxybenzyl-4-hydroxyphenylsulfonium hexafluorophosphate Salt; p-chlorobenzyl-4-hydroxyphenylmethylsulfonium hexa Luoantimonate, p-nitrobenzyl-4-hydroxyphenylmethylsulfonium hexafluoroantimonate, 3,5-dichlorobenzyl-4-hydroxyphenylmethylsulfonium hexafluoroantimonate, o-chlorobenzyl-3-chloro-4- Examples thereof include substituted benzylsulfonium salts such as hydroxyphenylmethylsulfonium hexafluoroantimonate. These sulfonium salts may be used individually by 1 type, and may be used in combination of 2 or more type.

  The benzothiazolium salt is not particularly limited. For example, 3-benzylbenzothiazolium hexafluoroantimonate, 3-benzylbenzothiazolium hexafluorophosphate, 3-benzylbenzothiazolium tetrafluoroborate, Such as 3- (p-methoxybenzyl) benzothiazolium hexafluoroantimonate, 3-benzyl-2-methylthiobenzothiazolium hexafluoroantimonate, 3-benzyl-5-chlorobenzothiazolium hexafluoroantimonate Benzylbenzothiazolium salt. These benzothiazolium salts may be used individually by 1 type, and may be used in combination of 2 or more type.

  The tertiary amine compound is not particularly limited, and examples thereof include trimethylamine, triethylamine, tripropylamine, tributylamine, triethylenediamine, 1,4-diazabicyclo [2.2.2] octane, quinuclidine, and 3-quinuclidinol. And aliphatic tertiary amines; aromatic tertiary amines such as dimethylaniline; and heterocyclic tertiary amines such as isoquinoline, pyridine, collidine, and betapicoline. These tertiary amine compounds may be used individually by 1 type, and may be used in combination of 2 or more type.

  As a suitable example of the said hardening accelerator, what functions as a thermal acid generator is mentioned. A thermal acid generator is a substance that generates an acid by heating and functions as a curing accelerator. Specific examples of the curing accelerator that can function as a thermal acid generator include sulfonium salts and benzothiazolium salts.

  In addition, another suitable example of the curing accelerator is a thermal latent that is activated under a predetermined heating condition (for example, 80 to 2000 ° C., preferably 100 to 160 ° C.) to promote the crosslinking reaction of the thermosetting resin. The thing with sex is mentioned. Among the above-mentioned curing accelerators, specific examples of the heat-latent substance include an epoxy adduct obtained by adding an epoxy compound to an amidine compound, a hydrazine compound, a tertiary amine compound, or the like.

  Furthermore, as another preferable example of the curing accelerator, it does not function as a curing agent in a sealed state, that is, in a moisture blocking state, but the sealed state is opened and hydrolyzed under the presence of moisture as a curing agent. Those having a hydrolytic potential that functions. Among the above-mentioned curing accelerators, specific examples of the hydrolytic latent substance include an epoxy adduct obtained by adding an epoxy compound to an amidine compound, a hydrazine compound, a tertiary amine compound, or the like.

  These hardening accelerators may be used individually by 1 type, and may be used in combination of 2 or more type. Among these curing accelerators, an amidine compound and a sulfonium salt are preferable, and an amidine compound is more preferable.

  About content of the hardening accelerator in the resin composition used for formation of the coating layer 1, although it sets suitably according to the kind of thermosetting resin to be used, the kind of hardening accelerator, etc., for example, thermosetting The curing accelerator is 0.01 to 6 parts by mass, preferably 0.05 to 5 parts by mass, and more preferably 0.1 to 2 parts by mass with respect to 100 parts by mass of the conductive resin.

(Reactive resin beads)
In the coating layer 1 having a single layer structure or in at least one layer constituting the coating layer 1 having a multilayer structure, the resin composition used for the formation is a reactive resin together with the thermosetting resin and the curing accelerator. Contains beads. In this way, by containing reactive resin beads in at least one layer constituting the coating layer 1, the reactive resin beads are chemically bonded to the thermosetting resin in the layer, and the battery packaging material is formed. It becomes possible to provide excellent moldability.

  The reactive resin beads are resin particles (filler) having a functional group that reacts with the thermosetting resin and chemically binds.

  The type of the functional group of the reactive resin bead used in the present invention is appropriately set according to the type of the thermosetting resin. For example, a hydroxyl group, a carboxyl group, an isocyanate group, a mercapto group, a hydrolyzable group. Examples thereof include a silyl group, an epoxy group, a polymerizable vinyl group, and a (meth) acryloyl group. Further, in the reactive resin beads, the number of functional groups per one is not particularly limited, but from the viewpoint that the reactive resin beads are stably held in the adhesive layer and exhibit excellent moldability. It is preferable to have two or more functional groups per bead. More specifically, in the case of reactive resin beads having a hydroxyl group, the hydroxyl value is, for example, 1 to 100 KOHmg / g, preferably 5 to 80 KOHmg / g. In the case of reactive resin beads having an isocyanate group (-N = C = O), the N = C = O content is 1 to 10% by weight, preferably 3 to 8% by weight. Further, in the case of reactive resin beads having a functional group other than the hydroxyl value and isocyanate group, the functional group equivalent (value obtained by dividing the molecular weight of the reactive resin beads by the functional group) is 100 to 5000, preferably 150 to 3000.

  Although it does not restrict | limit especially about resin which comprises the particle | grains of a reactive resin bead, For example, a urethane resin, an acrylic resin, a urethane acrylic resin, a nylon resin etc. are mentioned. Among these, Preferably, a urethane resin and an acrylic resin are mentioned.

  From the viewpoint of further improving moldability, the reactive resin beads of the present invention preferably include urethane beads having a hydroxyl group and / or an isocyanate group as functional groups, and acrylic beads having a hydroxyl group and / or an isocyanate group.

  Further, the refractive index of the reactive resin beads is not particularly limited, but from the viewpoint of providing the coating layer 1 with excellent transparency, for example, 1.3 to 1.8, preferably 1.4 to 1.6. Is mentioned. Here, the refractive index of the reactive resin beads is a value measured according to B method of JIS K7142 “Method for measuring refractive index of plastic”. Further, the closer the refractive index of the reactive resin bead to the thermosetting resin used, the more difficult it is to visually recognize the presence of the reactive resin bead in the coating layer 1, and the coating layer 1 has more excellent transparency. be able to.

  Further, the average particle diameter of the reactive resin beads is not particularly limited, but may be, for example, 0.1 to 15 μm, preferably 0.2 to 10 μm, from the viewpoint of further improving the film strength and moldability. The average particle size of the reactive resin beads is measured by using the Shimadzu laser diffraction particle size distribution analyzer SALD-2100-WJA1 and using compressed air to inject the powder to be measured from the nozzle and into the air. It is a value measured by an injection-type dry measurement method that is measured by dispersing.

  As such reactive resin beads, for example, Art Pearl C-TH series (hydroxyl group-added urethane beads), Art Pearl RU to RV series (reactive urethane beads to block NCO type), etc. (all of which are Negami Kogyo Co., Ltd.) Manufactured) are commercially available, and these commercially available products can also be used.

  These reactive resin beads may be used alone or in a combination of two or more.

  In the resin composition used for forming at least one layer constituting the coating layer 1, the content of the reactive resin beads depends on the type of thermosetting resin used, the type of reactive resin beads, and the like. Although it sets suitably, for example with respect to 100 mass parts of thermosetting resins, a reactive resin bead is 0.1-30 mass parts in total, Preferably 0.2-15 mass parts is mentioned.

(Pigments and / or dyes)
The at least one layer constituting the coating layer 1 may contain a pigment and / or a dye as necessary. By including a pigment and / or dye in at least one layer constituting the coating layer 1, the battery packaging material can be given distinctiveness (colored by the pigment and / or dye), and further the battery packaging material. The heat conductivity can be increased to improve the heat dissipation.

  The material of the pigment is not particularly limited and may be either an inorganic pigment or an organic pigment. Specific examples of inorganic pigments include carbon black, carbon nanotube, graphite, talc, silica, kaolin, montmorillonite, montmorillonite, synthetic mica, hydrotalcite, zeolite, aluminum hydroxide, magnesium hydroxide, zinc oxide, and oxidation. Examples include magnesium, aluminum oxide, neodymium oxide, antimony oxide, titanium oxide, cerium oxide, calcium sulfate, barium sulfate, calcium carbonate, calcium silicate, lithium carbonate, gold, aluminum, copper, nickel, and the like. Specific examples of the organic pigment include azo pigments, polycyclic pigments, lake pigments, and fluorescent pigments. These pigments may be used alone or in combination of two or more.

  The shape of the pigment is not particularly limited, and examples thereof include a spherical shape, a fiber shape, a plate shape, an indefinite shape, and a balloon shape. Further, the average particle diameter of the pigment is not particularly limited, but for example, 0.01 to 3 μm, preferably 0.05 to 1 μm. The average particle size of the pigment is determined by using the Shimadzu laser diffraction particle size distribution analyzer SALD-2100-WJA1 and using compressed air to inject the powder to be measured from the nozzle and dispersing it in the air. It is a value measured by the jet type dry measurement method to be measured.

  If necessary, the pigment may be subjected to various surface treatments such as insulation treatment and high dispersibility treatment (resin coating treatment) on the surface.

  The type of the dye is not particularly limited as long as it can be dissolved and dispersed in the resin composition used for forming the coating layer 1. For example, nitro dye, azo dye, stilbene dye, carbonium dye, quinoline Examples thereof include dyes, methine dyes, thiazole dyes, quinimine dyes, anthraquinone dyes, indigoid dyes, and phthalocyanine dyes, and preferred examples include azo dyes, carbonium dyes, and anthraquinone dyes. These dyes may be used alone or in combination of two or more.

  Among these pigments and dyes, from the viewpoint of further improving the heat dissipation of the battery packaging material, preferably a pigment, more preferably an inorganic pigment, more preferably a carbon material such as carbon black, carbon nanotube, and graphite, particularly Preferably, carbon black is used.

  When the pigment and / or dye is contained in at least one layer constituting the coating layer 1, the content of the pigment and / or the dye used, the distinguishability to be imparted to the battery packaging material, and heat dissipation It may be set as appropriate according to the properties, etc., for example, the pigment and / or dye is 1 to 30 parts by mass in total with respect to 100 parts by mass of the thermosetting resin contained in the layer containing the pigment and / or dye. Is mentioned. From the viewpoint of imparting even better discrimination, the total amount of pigment and / or dye is 3 to 20 parts by mass with respect to 100 parts by mass of the thermosetting resin contained in the layer containing the pigment and / or dye. Can be mentioned. Moreover, from the viewpoint of suppressing the deterioration of the moldability caused by the pigment and / or dye together with the further excellent discrimination, with respect to 100 parts by mass of the thermosetting resin contained in the layer containing the pigment and / or dye. In addition, the total amount of pigment and / or dye is 5 to 15 parts by mass.

(Other additives)
In addition to the components described above, the resin composition used for forming the coating layer 1 may contain other additives such as an organic filler, a slip agent, a solvent, and an elastomer resin as necessary.

  In particular, when the coating layer 1 has a single-layer structure, or a slip agent is contained in a layer located in the outermost layer in a multi-layer structure, the molding / workability in press molding or embossing can be improved, It becomes possible to improve the property.

  The type of the organic filler is not particularly limited, and examples thereof include high melting point nylon, crosslinked acrylic, crosslinked styrene, crosslinked polyethylene, and benzoguanamine. The shape of the organic filler is not particularly limited, and examples thereof include a spherical shape, a fiber shape, a plate shape, an indeterminate shape, and a balloon shape.

  Moreover, it does not restrict | limit especially as a slip agent, A non-reactive slip agent may be sufficient and a reactive slip agent may be sufficient. In particular, the reactive slip agent is less likely to lose bleed from the coating layer 1, and can suppress powder blowing and set-off during use or a reduction in the slip effect of the coating layer 1 over time. Among these slip agents, a reactive slip agent is preferable because of its advantage.

  Here, the non-reactive slip agent is a compound that does not have a functional group that chemically reacts with the thermosetting resin and can impart slip properties (slip properties). The reactive slip agent is a compound that has a functional group that reacts with the thermosetting resin and chemically binds, and can impart slip properties (slip properties).

  Specific examples of the non-reactive slip agent include fatty acid amide, metal soap, hydrophilic silicone, silicone-grafted acrylic, silicone-grafted epoxy, silicone-grafted polyether, silicone-grafted polyester, Examples thereof include block type silicone acrylic copolymer, polyglycerol-modified silicone, paraffin and the like. These non-reactive slip agents may be used individually by 1 type, and may be used in combination of 2 or more type.

  In the reactive slip agent, the type of functional group is appropriately set according to the type of thermosetting resin to be used. For example, hydroxyl group, mercapto group, hydrolyzable silyl group, isocyanate group, epoxy group A polymerizable vinyl group, a (meth) acryloyl group, and the like. In the reactive slip agent, the number of functional groups per molecule is not particularly limited, and examples thereof include 1 to 3, preferably 1 or 2.

  Specific examples of reactive slip agents include modified silicones having the above functional groups; modified fluororesins having the above functional groups; fatty acid amides such as stearic acid amide, oleic acid amide, erucic acid amide, and ethylene bis-stearic acid amide. On the other hand, there can be mentioned compounds having the functional group introduced therein; metal soaps having the functional group introduced therein; paraffins having the functional group introduced therein. These reactive slip agents may be used individually by 1 type, and may be used in combination of 2 or more type. Among these reactive slip agents, the modified silicone having the functional group, the fluororesin having the functional group, and the silicone-modified resin having the functional group are preferable. As the modified silicone, specifically, a modified silicone obtained by block polymerization of a polymer having the functional group, such as a modified silicone obtained by block polymerization of an acrylic resin; a modified silicone obtained by graft polymerization of an acrylate, or the like, Examples thereof include modified silicone obtained by graft polymerization of a monomer having a functional group. Further, as the modified fluororesin, specifically, a modified fluororesin in which a monomer having the functional group is graft-polymerized, such as a fluororesin in which acrylate is graft-polymerized; modified fluorine in which an acrylic resin is block-polymerized Examples of the resin include a fluororesin in which a polymer having the functional group is block polymerized. Further, as the silicone-modified resin, specifically, the silicone having a functional group and the silicone having undergone graft polymerization, such as a silicone-modified acrylic resin in which silicone is graft-polymerized to the acrylic resin having the functional group. Examples include silicone-modified resins. Further, as the modified fluororesin, specifically, a modified fluororesin in which a monomer having the functional group is graft-polymerized, such as a fluororesin in which acrylate is graft-polymerized; modified fluorine in which an acrylic resin is block-polymerized Examples of the resin include a fluororesin in which a polymer having the functional group is block polymerized. Among these, as a particularly preferable reactive slip agent, a modified silicone in which the monomer or polymer having the functional group is polymerized at one terminal of the silicone; the monomer or polymer having the functional group is fluorine. Examples thereof include a modified fluororesin that is polymerized at one end of the resin. As such modified silicone and modified fluororesin, for example, “Modiper (registered trademark) F / FS series” (manufactured by NOF Corporation), “Symac (registered trademark) series” (manufactured by Toagosei Co., Ltd.) and the like are commercially available. These commercial products can also be used.

  These slip agents may be used individually by 1 type, and may be used in combination of 2 or more type.

  When the coating layer 1 has a single layer structure, or a slip agent is included in a layer located in the outermost layer in a multilayer structure, the content is not particularly limited, but for example, 100 parts by mass of a thermosetting resin In contrast, the total amount of slip agent is 1 to 12 parts by mass, preferably 3 to 10 parts by mass, and more preferably 5 to 8 parts by mass.

  When the coating layer 1 has a multilayer structure, an elastomer resin is applied to a layer other than the layer located on the outermost surface (that is, the layer provided between the outermost layer constituting the coating layer 1 and the barrier 2). When contained, the coating layer 1 can be imparted with appropriate flexibility while suppressing shrinkage of the coating layer 1 during curing, and the moldability can be further improved.

  The elastomer resin has a functional group that can be cross-linked with the thermosetting resin, and may be cross-linked with the thermosetting resin when cured, and does not have such a functional group. Even if cured, it may not be crosslinked with the thermosetting resin. The type of elastomer resin is not particularly limited. For example, a polyolefin-based elastomer such as ethylene-based elastomer containing ethylene and one or more α-olefins (excluding ethylene) having 2 to 20 carbon atoms as constituent monomers. Elastomers; Styrenic elastomers; Polyester elastomers; Urethane elastomers; Acrylic elastomers; Epoxy elastomers such as bisphenol A type epoxy elastomers; Polyol elastomers such as polyester polyols, polyester polyurethane polyols, polyether polyols, and polyether polyurethane polyols ; Rubber components such as nitrile rubber, fluorine rubber, acrylic rubber, silicone rubber, chloroprene rubber, isoprene rubber, butadiene rubber, etc.Among these elastomer resins, a urethane elastomer, an epoxy elastomer, and a polyol elastomer are preferable.

  These elastomer resins may be used individually by 1 type, and may be used in combination of 2 or more type.

  When the coating layer 1 has a multilayer structure, an elastomer resin is contained in a layer other than the layer located on the outermost surface (that is, the layer provided between the outermost layer constituting the coating layer 1 and the barrier 2) When it is made, the content is not particularly limited, but for example, the total amount of slip agent is 3 to 50 parts by weight, preferably 5 to 30 parts by weight, more preferably 10 to 100 parts by weight of the thermosetting resin. -20 mass parts is mentioned.

(Suitable layer structure of coating layer 1)
As described above, the coating layer 1 may have a single-layer structure or a multi-layer structure including two or more layers. However, in order to provide a thick film that can provide sufficient insulation. , Preferably a multilayer structure composed of two or more layers, more preferably a multilayer structure composed of two or three layers, particularly preferably a multilayer structure composed of three layers.

  When the coating layer 1 has a multi-layer structure composed of two layers, the reactive resin beads may be included in any one of these layers, or included in both of these layers. However, the reactive resin beads are preferably contained only in the layer located on the outermost surface. That is, when the coating layer 1 has a two-layer structure in which the first coating layer 1a and the second coating layer 1b are arranged in this order from the outermost surface side toward the barrier layer 2, the coating layer 1 and the barrier layer 2 From the viewpoint of improving adhesion, the first coating layer 1a preferably contains the reactive resin beads, and the second coating layer 1b preferably does not contain the reactive resin beads. When the pigment and / or dye is contained in the coating layer 1 having such a two-layer structure, the pigment and / or dye is at least one of the first coating layer 1a and the second coating layer 1b. It only has to be included in the layer. From the viewpoint of reducing the difference in color tone between the molded part and the non-molded part after the battery packaging material is molded, the pigment and / or the dye are both in the first coating layer 1a and the second coating layer 1b. It is preferable that it is contained.

  In addition, when the coating layer 1 is a multilayer composed of three layers, the reactive resin beads may be included in any one of these layers, and two of these layers may be included. Although it may be contained above, it is preferable that the reactive resin bead is contained only in the layer arranged at the center of the three layers. That is, when the coating layer 1 has a three-layer structure in which the first coating layer 1a, the second coating layer 1b, and the third coating layer 1c are arranged in this order from the outermost surface side toward the barrier layer 2, From the viewpoint of more effectively providing chemical resistance and slipping properties while improving the adhesion between the layer 1 and the barrier layer 2, the second coating layer 1b preferably contains the reactive resin beads. It is preferable that the reactive resin beads are not contained in the coating layer 1a and the third coating layer 1c. Further, when the pigment is contained in the coating layer 1 having such a three-layer structure, the pigment and / or the dye is any one of the first coating layer 1a, the second coating layer 1b, and the third coating layer 1c. It may be contained in at least one layer. From the viewpoint of reducing the difference in color tone between the molded part and the non-molded part after the molding of the battery packaging material, the pigment and / or the dye may be the first coating layer 1a, the second coating layer 1b, and It is preferably contained in at least two layers in the third coating layer 1c, and more preferably contained in all these three layers.

(Thickness of coating layer 1)
Although it does not restrict | limit especially about the thickness of the coating layer 1 whole, For example, 4-20 micrometers, Preferably 6-18 micrometers is mentioned. More specifically, if the coating layer 1 has a single layer structure, the thickness is, for example, 2 to 10 μm, preferably 3 to 7 μm. Moreover, if the coating layer 1 has a multilayer structure composed of two or more layers, the thickness of each layer alone is, for example, 1 to 5 μm, preferably 2 to 4 μm.

[Barrier layer 2]
In the battery packaging material of the present invention, the barrier layer 2 is a layer that functions as a barrier layer for preventing moisture, oxygen, light, and the like from entering the battery, in addition to improving the strength of the packaging material. Specific examples of the material of the barrier layer 2 include metal foils such as aluminum, stainless steel, and titanium; films obtained by vapor deposition of inorganic compounds such as silicon oxide and alumina. Among these, metal foil is preferable, and aluminum foil is more preferable. In order to prevent wrinkles and pinholes during the production of battery packaging materials, the barrier layer 2 in the present invention is a soft aluminum foil, for example, annealed aluminum (JIS A8021P-O) or (JIS A8079P-O) foil. Etc. are preferably used.

  Although it does not restrict | limit especially about the thickness of the barrier layer 2, For example, when using metal foil, 10-200 micrometers normally, Preferably 20-100 micrometers is mentioned.

  Further, when a metal foil is used as the barrier layer 2, at least one surface, preferably at least the surface on the sealant layer side, and more preferably both surfaces are subjected to chemical conversion treatment in order to stabilize adhesion, prevent dissolution and corrosion, and the like. It is preferable. Here, the chemical conversion treatment is a treatment for forming an acid-resistant film on the surface of the barrier layer 2. Chemical conversion treatment is, for example, chromate chromate treatment using a chromic acid compound such as chromium nitrate, chromium fluoride, chromium sulfate, chromium acetate, chromium oxalate, chromium biphosphate, chromic acetyl acetate, chromium chloride, potassium sulfate chromium, etc. ; Phosphoric acid chromate treatment using phosphoric acid compounds such as sodium phosphate, potassium phosphate, ammonium phosphate, polyphosphoric acid; aminated phenol heavy consisting of repeating units represented by the following general formulas (1) to (4) Examples thereof include chromate treatment using a coalescence.

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

  Further, as a chemical conversion treatment method for imparting corrosion resistance to the metal foil, a metal oxide such as aluminum oxide, titanium oxide, cerium oxide, tin oxide or the like, in which fine particles of barium sulfate are dispersed in phosphoric acid, is coated. A method of forming a corrosion-resistant treatment layer on the surface of the metal foil by performing a baking treatment at a temperature of 0 ° C. or higher can be mentioned. A resin layer obtained by crosslinking a cationic polymer with a crosslinking agent may be formed on the corrosion-resistant treatment 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 the aminated phenol polymer are combined is more preferable.

The amount of the acid-resistant film to be formed on the surface of the metal foil in the chemical conversion treatment is not particularly limited. For example, if the chromate treatment is performed by combining a chromic acid compound, a phosphoric acid compound, and the 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 foil. About 1.0 to about 40 mg, and the aminated phenol polymer is desirably contained in an amount of about 1 to about 200 mg, preferably about 5.0 to 150 mg.

  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 foil by a bar coating method, a roll coating method, a gravure coating method, a dipping method or the like, and then the temperature of the metal foil is 70. It is carried out by heating to about 200 ° C. In addition, before the chemical conversion treatment is performed on the barrier layer 2, the metal foil 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 foil.

[Adhesive layer 4]
In the battery packaging material of the present invention, the adhesive layer 4 is a layer provided between the barrier layer 2 and the sealant layer 3 as necessary in order to firmly bond them.

  The adhesive layer 4 is formed of an adhesive resin composition that can adhere the barrier layer 2 and the sealant layer 3. The adhesive component used for forming the adhesive layer 4 is not particularly limited as long as the barrier layer 2 and the sealant layer 3 can be bonded, and may be a two-component curable adhesive. A curable adhesive may be used. Further, the adhesion mechanism of the adhesive component used for forming the adhesive layer 4 is not particularly limited, and may be any of a chemical reaction type, a solvent volatilization type, a heat melting type, a hot pressure type, and the like. Polyester resins such as polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, polybutylene naphthalate, polyethylene isophthalate, polycarbonate, and copolyester; polyether adhesives; polyurethane adhesives; epoxy resins; phenol resin resins Polyamide resins such as nylon 6, nylon 66, nylon 12 and copolymerized polyamides; polyolefin resins such as polyolefins, carboxylic acid modified polyolefins, metal modified polyolefins, polyvinyl acetate resins; cellulose adhesives; (meth) acrylic Tree ; Polyimide resin; urea resins, amino resins such as melamine resins; - chloroprene rubbers, nitrile rubbers, styrene rubbers such as butadiene rubber, silicone-based resins.

  In the formation of the adhesive layer 4, from the viewpoint of shortening the lead time by curing in a short time without requiring aging under high temperature conditions during production, and further improving the moldability, preferably thermosetting A resin composition for an adhesive layer containing a resin and a curing accelerator is preferably used. By using a thermosetting resin and a curing accelerator in combination, the lead time can be shortened by curing in a short time without requiring aging under high temperature conditions.

  About the kind of thermosetting resin used for the said resin composition for contact bonding layers, a preferable thing, etc., it is the same as that of the thermosetting resin as described in the said [Coating layer 1] column. In addition, the types and preferred curing accelerators used in the adhesive layer resin composition are the same as the curing accelerators described in the column “Coating layer 1”. About content of the hardening accelerator in the said resin composition for contact bonding layers, although suitably set according to the kind of thermosetting resin to be used, the kind of hardening accelerator, etc., for example, 100 mass parts of thermosetting resins In contrast, the total amount of the curing accelerator is 0.01 to 6 parts by mass, preferably 0.05 to 5 parts by mass, and more preferably 0.1 to 2 parts by mass.

  About the thickness of the contact bonding layer 4, 2-50 micrometers, for example, Preferably 3-25 micrometers is mentioned.

[Sealant layer 3]
In the battery packaging material of the present invention, the sealant layer 3 corresponds to the innermost layer and is a layer that seals the battery element by heat-sealing the sealant layers when the battery is assembled.

  The resin component used in the sealant layer 3 is not particularly limited as long as it can be thermally welded, and examples thereof include polyolefin, cyclic polyolefin, carboxylic acid-modified polyolefin, and carboxylic acid-modified cyclic polyolefin.

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

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

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

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

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

  The sealant layer 3 may be formed of one kind of resin component alone or may be formed of a blend polymer in which two or more kinds of resin components are combined. Furthermore, the sealant layer may be formed of only one layer, but may be formed of two or more layers using the same or different resin components.

  Further, the thickness of the sealant layer 3 is not particularly limited, but may be 2 to 2000 μm, preferably 5 to 1000 μm, and more preferably 10 to 500 μm.

[Battery packaging material thickness]
Since the battery packaging material of the present invention does not have a base layer made of an adhesive layer and a resin film on the barrier layer 3, it can be made thinner than conventional film-shaped battery packaging materials. About the thickness of the whole battery packaging material of this invention, 40-120 micrometers is mentioned, for example, Preferably 50-100 micrometers is mentioned.

3. 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. :
A coating layer forming step of applying a resin composition containing a thermosetting resin and a curing accelerator on the barrier layer 2 and heating to cure;
The coating layer forming step is performed once or a plurality of times, and at least once in the coating layer forming step, the resin composition containing reactive resin beads is used,
Before or after the coating layer forming step, the sealant layer 3 is laminated on the surface of the barrier layer 2 opposite to the surface on which the coating layer 1 is laminated.

  Application | coating of the resin composition which forms the coating layer to the barrier layer 2 in the said coating layer formation process can be performed with application methods, such as a gravure coat method and a roll coat method. Moreover, as a heating condition at the time of hardening the resin composition apply | coated on the barrier layer 2, it is 90-200 degreeC, for example, Preferably it is 100-190 degreeC, 0.1 to 60 second, Preferably it is 1 to 30 second Is mentioned.

  As described above, in the present invention, the aging under the high temperature condition is not required in the coating layer forming step, and the slip coating layer 1 can be sufficiently cured only by the heating condition, thereby greatly reducing the lead time. be able to.

  When the sealant layer 3 is directly laminated on the barrier layer 2, the resin component constituting the sealant layer 3 may be applied on the barrier layer 2 by a method such as a gravure coating method or a roll coating method. When the adhesive layer 4 is provided between the barrier layer 2 and the sealant layer 3, for example, (1) a method of laminating the adhesive layer 4 and the sealant layer 3 on the barrier layer 2 by coextrusion (co- Extrusion lamination method), (2) Separately, a laminate in which the adhesive layer 4 and the sealant layer 3 are laminated, and this is laminated on the barrier layer 2 by the thermal lamination method. (3) On the barrier layer 2, An adhesive for forming the adhesive layer 4 is laminated by an extrusion method, a solution-coated high temperature drying or baking method, and the sealant layer 3 previously formed into a sheet shape on the adhesive layer 4 by a thermal lamination method. (4) Laminate A and sealant layer 3 through adhesive layer 4 while pouring molten adhesive layer 4 between barrier layer 2 and sealant layer 3 formed into a sheet in advance. Be bonded method (sand lamination method), and the like.

  As described above, a single layer or multi-layered coating layer 1 / a laminated body comprising a barrier layer 2 whose surface is subjected to chemical conversion treatment as required / an adhesive layer 4 provided as necessary / a sealant layer 3 is formed. Is done.

  In the battery packaging material of the present invention, each layer constituting the laminate is improved or stabilized as necessary in terms of film-forming properties, lamination processing, suitability for final processing (pouching, embossing), etc. In order to do so, surface activation treatment such as corona treatment, blast treatment, oxidation treatment, ozone treatment, etc. may be performed.

4). Application of Battery Packaging Material The battery packaging material of the present invention is used by being molded into a desired shape as a packaging material for sealing and housing battery elements such as a positive electrode, a negative electrode, and an electrolyte.

  Specifically, a battery element including at least a positive electrode, a negative electrode, and an electrolyte is formed 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 packaging material was used by covering the periphery of the element so that a flange portion (a region where the sealant layers 3 contact each other) can be formed, and heat sealing the sealant layers 3 of the flange portion together. A battery is provided. In addition, when accommodating a battery element using the battery packaging material of the present invention, the battery packaging material of the present invention is used such that the sealant portion 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.

  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.

(1) Manufacture and evaluation of battery packaging materials having a two-layer coating layer-1
[Manufacture of battery packaging materials 1]
A coating layer having a two-layer structure was formed on a barrier layer made of an aluminum foil (thickness: 40 μm) subjected to chemical conversion treatment on both sides. Specifically, the resin composition A2 having the following composition was applied to the barrier layer so that the thickness after curing was 5 μm, and cured under the conditions of 120 ° C. and 30 seconds to form a second coating layer. Next, on the second coating layer, a resin composition A1 having the following composition was applied so that the thickness after curing was 5 μm, and cured at 120 ° C. for 30 seconds to form a first coating layer. . In addition, the chemical conversion treatment of the aluminum foil used as the barrier layer was performed by roll coating a treatment liquid composed of a phenol resin, a chromium fluoride compound, and phosphoric acid so that the coating amount of chromium was 10 mg / m ² (dry weight). The coating was performed on both surfaces of the aluminum foil by the method and baked for 20 seconds under the condition that the film temperature was 180 ° C. or higher.

  Thereafter, the barrier layer is formed by co-extruding carboxylic acid-modified polypropylene (arranged on the barrier layer side, thickness 23 μm) and homopolypropylene (innermost layer, thickness 23 μm) on the side of the barrier layer where the coating layer is not laminated. A two-layer sealant layer was laminated on the layer. Thus, a battery packaging material comprising a laminate in which a coating layer having a two-layer structure (first coating layer / second coating layer) / barrier layer 4 / sealant layer was sequentially laminated was obtained.

<Resin composition A2 used for forming the second coating layer>
・ 100 parts by mass of thermosetting resin (main agent: urethane polyol having a molecular weight of 8000 to 50000 and a hydroxyl value of less than 40, curing agent: diphenylmethane diisocyanate adduct)
-Curing accelerator 1 part by mass (imidazole compound that promotes crosslinking reaction of thermosetting resin at 80-150 ° C)

<Resin composition A1 used for forming the first coating layer>
-Thermosetting resin 100 parts by mass (main agent: aliphatic polyol having a molecular weight of 500 to 3000 and a hydroxyl value of 70 or more, curing agent: diphenylmethane diisocyanate adduct)
Curing accelerator 1 part by mass (octylate salt of 1,8-diazabicyclo [5.4.0] undec-7ene)
Resin beads Predetermined amounts shown in Tables 1 to 4 (resin beads shown in Tables 1 to 4)
・ Slip agent 1 part by mass (erucic amide)

[Manufacture of battery packaging materials 2]
In the formation of the first coating layer, a battery packaging material was produced in the same manner as in [Manufacture of battery packaging material 1] except that the resin composition B1 having the following composition was used.

<Resin composition B1 used for forming the first coating layer>
・ 100 parts by mass of thermosetting resin (main agent: urethane polyol having a molecular weight of 8000 to 50000 and a hydroxyl value of less than 40, curing agent: diphenylmethane diisocyanate adduct)
Curing accelerator 1 part by mass (octylate salt of 1,8-diazabicyclo [5.4.0] undec-7ene)
Resin beads Predetermined amounts shown in Tables 1 to 4 (resin beads shown in Tables 1 to 4)

[Evaluation of formability]
Each battery packaging material obtained above was cut into 120 × 80 mm strips, which were used as test samples. Using a straight mold composed of a 30 × 50 mm rectangular male mold and a female mold with a clearance of 0.5 mm between the male mold and the above, the thermal adhesive resin layer side is positioned on the male mold side. The test sample was placed, the forming depth was set in various ranges, and the test sample was pressed with a presser pressure (surface pressure) of 0.1 MPa to perform cold forming (retraction one-step forming). The presence or absence of pinholes and cracks in the metal layer in each of the molded test samples was confirmed, and the pinhole and crack generation rates (%) were calculated. The incidence of pinholes and cracks was determined when molding was performed when 100 test samples were molded under the above-mentioned conditions by determining that pinholes or cracks were observed even at one location after molding as above. The proportion of defective products was determined, and the case where the proportion of molding defects was less than 5% was judged as acceptable, and the case where the proportion of molding defects was 5% or more was judged as unacceptable. In addition, the moldability was similarly evaluated using the battery packaging material produced in the same manner as described above except that no resin beads were added to the resin composition forming the first coating layer. The obtained results were judged according to the following criteria, and the moldability improvement effect was evaluated.

(Criteria for moldability improvement effect)
(Double-circle): The shaping | molding depth used as a pass is improved by 1.0 mm or more compared with control.
○: The forming depth that is acceptable as compared with the control is improved by 0.5 mm or more and less than 1.0 mm.
(Triangle | delta): The shaping | molding depth used as the pass is the same as control.
X: The forming depth that is acceptable is lower than that of the control.

[Evaluation results]
The obtained results are shown in Tables 1 to 4. As is clear from Tables 1 to 4, when resin beads that do not have reactivity are added to the resin composition that forms one of the coating layers, it is compared with the case where resin beads are not added. As a result, the moldability was reduced (Comparative Examples 1 to 4). On the other hand, when reactive resin beads are added to the resin composition forming one layer of the coating layer, the molding depth can be increased compared to when no resin beads are added. It was found that the moldability was improved. In addition, by adding a curing accelerator to the resin composition forming the coating layer, the adhesive layer can be cured in an extremely short time of 160 ° C. for 30 seconds, and the lead time can be greatly shortened. (Examples 1 to 50).

(2) Manufacture and evaluation of battery packaging materials having a three-layer coating layer-1
[Manufacture of battery packaging materials 3]
A coating layer having a three-layer structure was formed on a barrier layer made of an aluminum foil (thickness 40 μm) subjected to chemical conversion treatment on both sides. Specifically, a resin composition C3 having the following composition was applied to the barrier layer so that the thickness after curing was 5 μm, and cured under the conditions of 120 ° C. and 30 seconds to form a third coating layer. Next, on the third coating layer, a resin composition C2 having the following composition was applied so that the thickness after curing was 5 μm, and cured at 120 ° C. for 30 seconds to form a second coating layer. . Furthermore, on the said 2nd coating layer, the resin composition C1 of the following composition was apply | coated so that the thickness after hardening might be set to 5 micrometers, and it hardened | cured on 120 degreeC and the conditions for 30 second, and formed the 1st coating layer. . In addition, the chemical conversion treatment of the aluminum foil used as the barrier layer was performed by roll coating a treatment liquid composed of a phenol resin, a chromium fluoride compound, and phosphoric acid so that the coating amount of chromium was 10 mg / m ² (dry weight). The coating was performed on both surfaces of the aluminum foil by the method and baked for 20 seconds under the condition that the film temperature was 180 ° C. or higher.

  Thereafter, the barrier layer is formed by co-extruding carboxylic acid-modified polypropylene (arranged on the barrier layer side, thickness 23 μm) and homopolypropylene (innermost layer, thickness 23 μm) on the side of the barrier layer where the coating layer is not laminated. A two-layer sealant layer was laminated on the layer. Thus, a battery packaging material comprising a laminate in which a three-layer coating layer (first coating layer / second coating layer / third coating layer) / barrier layer 4 / sealant layer was sequentially laminated was obtained.

<Resin composition C3 used for forming the third coating layer>
・ 100 parts by mass of thermosetting resin (main agent: urethane polyol having a molecular weight of 8000 to 50000 and a hydroxyl value of less than 40, curing agent: diphenylmethane diisocyanate adduct)
Curing accelerator 1 part by mass (octylate salt of 1,8-diazabicyclo [5.4.0] undec-7ene)

<Resin composition C2 used for forming the second coating layer>
-Thermosetting resin 100 parts by mass (main agent: aliphatic polyol having a molecular weight of 500 to 3000 and a hydroxyl value of 70 or more, curing agent: isophorone diisocyanate)
-Curing accelerator 1 part by mass (imidazole compound that promotes crosslinking reaction of thermosetting resin at 80-150 ° C)
・ Resin beads Predetermined amounts shown in Tables 5 to 8 (Resin beads shown in Tables 5 to 8)

<Resin composition C1 used for forming the first coating layer>
・ 100 parts by mass of thermosetting resin (main agent: molecular weight 200-1000, phenol novolac type epoxy resin, curing agent: methylhexahydrophthalic anhydride)
Curing accelerator 1 part by mass (octylate salt of 1,8-diazabicyclo [5.4.0] undec-7ene)
・ Slip agent 1 part by mass (erucic amide)

[Manufacture of battery packaging materials 4]
In the formation of the second coating layer, a battery packaging material was produced in the same manner as in [Manufacture of battery packaging material 3] except that the resin composition D2 having the following composition was used.

<Resin composition D2 used for forming the second coating layer>
・ 100 parts by mass of thermosetting resin (main agent: molecular weight 200-1000, phenol novolac type epoxy resin, curing agent: methylhexahydrophthalic anhydride)
Curing accelerator 1 part by mass (octylate salt of 1,8-diazabicyclo [5.4.0] undec-7ene)
・ Resin beads Predetermined amounts shown in Tables 5 to 8 (Resin beads shown in Tables 5 to 8)

[Evaluation of formability]
The effect of improving the moldability of each battery packaging material was evaluated under the same conditions as in the case of “Manufacture and evaluation of battery packaging material having a coating layer having a 1.2 layer structure”.

[Evaluation results]
The obtained results are shown in Tables 5-8. From these results, in battery packaging materials having a three-layer coating layer, moldability is improved by adding reactive resin beads to the adhesive layer in the resin composition that forms one of the coating layers. (Examples 51 to 100). On the other hand, when resin beads having no reactivity were added to the resin composition forming one of the coating layers, the moldability was rather inferior (Comparative Examples 5 to 8). Also, from this test result, by adding a curing accelerator to the resin composition forming the coating layer, the adhesive layer can be cured in an extremely short time of 160 ° C. for 30 seconds, and lead time can be reduced. Examples 51 to 100) in which significant shortening was achieved.

(3) Manufacture and evaluation of battery packaging materials having a two-layer coating layer-2
[Manufacture of battery packaging materials 5]
[Manufacturing of battery packaging material 1], except that resin composition E1 having the following composition was used in forming the first coating layer and resin composition E2 having the following composition was used in forming the second coating layer. A battery packaging material was produced in the same manner as described above.

<Resin composition E2 used for forming the second coating layer>
・ 100 parts by mass of thermosetting resin (main agent: urethane polyol having a molecular weight of 8000 to 50000 and a hydroxyl value of less than 40, curing agent: diphenylmethane diisocyanate adduct)
-Curing accelerator 1 part by mass (imidazole compound that promotes crosslinking reaction of thermosetting resin at 80-150 ° C)
Inorganic pigment Predetermined amounts shown in Table 9 (carbon black average particle diameter 0.2 μm)

<Resin composition E1 used for forming the first coating layer>
-Thermosetting resin 100 parts by mass (main agent: aliphatic polyol having a molecular weight of 500 to 3000 and a hydroxyl value of 70 or more, curing agent: diphenylmethane diisocyanate adduct)
Curing accelerator 1 part by mass (octylate salt of 1,8-diazabicyclo [5.4.0] undec-7ene)
・ Resin beads 0.3 parts by mass (made of urethane resin, containing hydroxyl group as functional group, number of functional group bonds (hydroxyl value, KOH mg / g) 5, average particle size 0.2 μm, refractive index 1.5)
Inorganic pigment Predetermined amounts shown in Table 9 (carbon black, average particle size 0.2 μm)
・ Slip agent 1 part by mass (erucic amide)

[Evaluation of distinguishability]
About the obtained battery packaging material and the battery packaging material of Example 6 (when the resin composition A1 is used for forming the first coating layer), the color tone on the coating layer side is visually observed, and the coating layer The visibility of coloration (black) by the carbon black blended in was confirmed and evaluated according to the following criteria.

(Evaluation criteria for distinguishability)
A: It can be clearly visually recognized that the color is black.
B: It can be visually recognized slightly that it is black.
C: It cannot visually recognize that it is black.

[Evaluation of moldability]
About each obtained battery packaging material and the battery packaging material of Example 6 (when resin composition A1 is used for formation of the 1st coating layer), it shape | molds on the same conditions as the above, and by moldability and shaping | molding The color tone of the stretched part was evaluated according to the following criteria.

(Formability)
A: The forming depth to pass is the same as that of the control battery packaging material.
B: A reduction of 0.5 mm or less is recognized in the molding depth that is acceptable as compared with the battery packaging material for control.
C: A decrease in the molding depth that passes is less than 0.5 mm and 1.0 mm or less as compared with the control battery packaging material.
D: A reduction of more than 1.0 mm is observed in the molding depth to pass, as compared with the control battery packaging material.

  In addition, the battery packaging material of Example 6 (when resin composition A1 is used for formation of the 1st coating layer) was used as the battery packaging material for control. The battery packaging materials of Examples 101 to 118 are the battery packaging material of Example 6 (of the first coating layer) except that the resin composition used for forming the first coating layer contains carbon black. This is the same structure as when resin composition A1 is used for formation.

(Color tone of stretched part by molding)
A: No difference in color tone is observed between the stretched part and the non-stretched part.
B: A slight difference in color tone is recognized between the stretched portion and the non-stretched portion.
C: A clear difference in color tone is recognized between the stretched portion and the non-stretched portion.

[Evaluation results]
Table 9 shows the obtained results. From this result, it was confirmed that by adding an inorganic pigment (carbon black) to at least one layer constituting the coating layer, a color tone can be imparted to the battery packaging material so as to have discriminability. Moreover, it was also confirmed that a decrease in moldability can be effectively suppressed by setting the amount of the inorganic pigment to be added to 30 parts by mass or less, particularly 15 parts by mass or less per 100 parts by mass of the thermosetting resin. Furthermore, it became clear that the color difference between the molded part and the non-molded part can be effectively suppressed after molding by adding an inorganic pigment to both the two layers constituting the coating layer. . Moreover, when the thermal conductivity of the battery packaging material in which carbon black was added to the coating layer was measured, it was confirmed that it had a thermal conductivity of about 60 W / m · K or more and had excellent heat dissipation. It was.

(4) Manufacture and evaluation of battery packaging materials having a three-layer coating layer-2
[Manufacture of battery packaging materials 6]
The resin composition F1 having the following composition is used in the formation of the first coating layer, the resin composition F2 having the following composition is used in the formation of the second coating layer, and the resin composition having the following composition is formed in the formation of the third coating layer. A battery packaging material was produced in the same manner as in [Manufacture of battery packaging material 3], except that F3 was used.

<Resin composition F3 used for forming the third coating layer>
・ 100 parts by mass of thermosetting resin (main agent: urethane polyol having a molecular weight of 8000 to 50000 and a hydroxyl value of less than 40, curing agent: diphenylmethane diisocyanate adduct)
Curing accelerator 1 part by mass (octylate salt of 1,8-diazabicyclo [5.4.0] undec-7ene)
Inorganic pigment Predetermined amounts shown in Tables 10 and 11 (carbon black, average particle size 0.2 μm)

<Resin composition F2 used for forming the second coating layer>
-Thermosetting resin 100 parts by mass (main agent: aliphatic polyol having a molecular weight of 500 to 3000 and a hydroxyl value of 70 or more, curing agent: isophorone diisocyanate)
-Curing accelerator 1 part by mass (imidazole compound that promotes crosslinking reaction of thermosetting resin at 80-150 ° C)
・ Resin beads 0.3 parts by mass (made of urethane resin, containing hydroxyl group as functional group, number of functional group bonds (hydroxyl value, KOH mg / g) 5, average particle size 0.2 μm, refractive index 1.5)
Inorganic pigment Predetermined amounts shown in Tables 10 and 11 (carbon black, average particle size 0.2 μm)

<Resin composition F1 used for forming the first coating layer>
・ 100 parts by mass of thermosetting resin (main agent: molecular weight 200-1000, phenol novolac type epoxy resin, curing agent: methylhexahydrophthalic anhydride)
Curing accelerator 1 part by mass (octylate salt of 1,8-diazabicyclo [5.4.0] undec-7ene)
Inorganic pigment Predetermined amounts shown in Tables 10 and 11 (carbon black, average particle size 0.2 μm)
・ Slip agent 1 part by mass (erucic amide)

[Evaluation of distinguishability and moldability]
About each obtained battery packaging material and the battery packaging material of Example 56 (when the resin composition C2 is used for forming the second coating layer), the battery having the coating layer having the above-mentioned (3) two-layer structure is used. In the same manner as in “Manufacturing packaging material and its evaluation-2”, the discriminability and moldability were evaluated.

  In the evaluation of “moldability” in moldability, the battery packaging material of Example 56 (when the resin composition C2 was used for forming the second coating layer) was used as the control battery packaging material. The battery packaging material of Examples 119 to 160 is the battery packaging material of Example 56 (of the second coating layer) except that the resin composition used to form the second coating layer contains carbon black. This is the same structure as when the resin composition C2 is used for formation.

[Evaluation results]
The results obtained are shown in Tables 10 and 11. Also from this result, it was confirmed that by adding an inorganic pigment (carbon black) to at least one layer constituting the coating layer, a color tone can be imparted to the battery packaging material so as to have discriminability. Moreover, it was also confirmed that a decrease in moldability can be effectively suppressed by setting the amount of the inorganic pigment to be added to 30 parts by mass or less, particularly 15 parts by mass or less per 100 parts by mass of the thermosetting resin. Furthermore, by adding an inorganic pigment to at least two of the three layers constituting the coating layer, in particular, three layers, a difference in color tone between the molded part and the non-molded part can occur after molding. It was also revealed that it can be effectively suppressed. Moreover, when the thermal conductivity of the battery packaging material in which carbon black was added to the coating layer was measured, it was confirmed that it had a thermal conductivity of about 60 W / m · K or more and had excellent heat dissipation. It was.

DESCRIPTION OF SYMBOLS 1 Coating layer 1a 1st coating layer 1b 2nd coating layer 1c 3rd coating layer 2 Barrier layer 3 Sealant layer

Claims (12)

It consists of a laminate having at least a coating layer, a barrier layer, and a sealant layer in this order,
The coating layer is composed of a single layer or a multilayer structure formed of a cured product of a resin composition containing a thermosetting resin and a curing accelerator,
Reactive resin beads are included in the resin composition used to form at least one layer of the coating layer.
A battery packaging material characterized by the above.   The coating layer has a three-layer structure in which a first coating layer, a second coating layer, and a third coating layer are arranged in this order from the outermost surface side to the barrier layer side, and the formation of the second coating layer The battery packaging material according to claim 1, wherein the reactive resin beads are included in the resin composition used in a battery.   The battery packaging material according to claim 1 or 2, wherein the reactive resin beads are urethane resin beads or acrylic resin beads having a functional group.   The battery packaging material according to any one of claims 1 to 3, wherein the reactive resin beads have a refractive index of 1.3 to 1.8.   The battery packaging material according to any one of claims 1 to 4, wherein the resin composition used for forming at least one layer of the coating layer contains a pigment and / or a dye.   The battery packaging material according to claim 5, wherein the resin composition used for forming at least one layer of the coating layer contains an inorganic pigment.   The thermosetting resin is at least one selected from the group consisting of an epoxy resin, an amino resin, an acrylic resin, a urethane resin, a phenol resin, an unsaturated polyester resin, and an alkyd resin. A packaging material for a battery according to claim 1.   The curing accelerator is at least one selected from the group consisting of an amidine compound, a carbodiimide compound, a ketimine compound, a hydrazine compound, a sulfonium salt, a benzothiazolium salt, and a tertiary amine compound. The battery packaging material according to any one of 7 above.   The battery packaging material according to claim 1, wherein the barrier layer is a metal foil.   The battery packaging material according to any one of claims 1 to 9, wherein the entire thickness of the battery packaging material is 40 to 120 µm. A coating layer forming step of applying a resin composition containing a thermosetting resin and a curing accelerator on the barrier layer, and curing by heating;
The coating layer forming step is performed once or a plurality of times, and at least once in the coating layer forming step, the resin composition containing reactive resin beads is used,
Before or after the coating layer forming step, a sealant layer is laminated on the surface of the barrier layer opposite to the surface on which the coating layer is laminated.
A method for producing a packaging material for a battery.   The battery by which the battery element provided with the positive electrode, the negative electrode, and electrolyte at least is accommodated in the packaging material for batteries in any one of Claims 1-10.