JP2008024882A - Thermoplastic elastomer composition for sealant, molding material, and capacitor - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a thermoplastic elastomer composition for sealant, recyclable and imparting a sealing material excellent in strength, flexibility, resistance to solvent, gas permeation resistance and sealing performance. <P>SOLUTION: The invention relates to the thermoplastic elastomer composition for sealant substantially free from a plasticizer and softener, comprising (A) at least a kind of rubber components selected from a group comprising an ethylene-α-olefin copolymer rubber and an isobutylene-isoprene copolymer rubber, (B) at least a kind of thermoplastic resin components selected from a group comprising an α-olefin based crystalline thermoplastic resin, an α-olefin based amorphous thermoplastic resin and a cyclic olefin based thermoplastic resin, and (C) an inorganic compound, and obtained by dynamically heat-treating the raw material composition comprising 10-90 mass.% of the (A) rubber component to the 100 mass.% of the sum of the (A) rubber component and (B) the thermoplastic resin component, in the presence of a crosslinking agent (D). <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention relates to a thermoplastic elastomer composition for a sealing material, a molded member, and a capacitor.

  In various electric / mechanical parts, various sealing materials are used as members for partitioning at least a part thereof. For example, in an electrolytic capacitor (hereinafter simply referred to as “capacitor”), a capacitor element impregnated with an electrolytic solution is accommodated in an outer case made of a metal material having an opening at one end thereof. A sealing material is used to seal the opening. It is known that the characteristics of such a sealing material have a great influence on the performance deterioration of the capacitor accompanying the evaporation and diffusion of the electrolytic solution. Therefore, it is very important to select the type of electrolyte and a sealing material having physical properties adapted to it.

  Conventionally, a rubber material mainly composed of butyl rubber has been used as a material constituting such a sealing material (see, for example, Patent Documents 1 and 2). However, a sealing material using a rubber material containing butyl rubber as a main component may not have sufficient solvent resistance. In order to improve the characteristics of such butyl rubber, it is disclosed that a resin-crosslinked butyl rubber obtained by crosslinking butyl rubber using an alkylphenol formalin resin as a crosslinking agent is used as a sealing material for a capacitor (for example, see Patent Document 3). .

  In addition, for the purpose of improving solvent resistance and the like, an attempt has been made to configure a capacitor sealing material using a resin material obtained by curing a saturated hydrocarbon polymer with a specific curing agent (for example, Patent Documents). 4). However, it has not been said that a capacitor sealing material composed of a resin material is superior in flexibility and sealing properties compared to a rubber sealing material.

  On the other hand, a thermoplastic elastomer composition containing a polyolefin-based thermoplastic resin and a crosslinked butyl rubber, and a capacitor part (sealant) using the same (for example, see Patent Document 5), an ink tube for an inkjet printer ( Tube material) (see, for example, Patent Document 6). However, even the sealing material made of the thermoplastic elastomer composition disclosed in Patent Document 5 has satisfactory properties such as strength, flexibility, solvent resistance, gas permeation resistance, and sealing properties. It wasn't. In addition, from the viewpoint of environmental protection in recent years, the importance of being recyclable is also increasing for materials constituting various electric and mechanical parts. The constituent material of the sealing material is no exception and is required to be recyclable. However, no material that can be recycled at the same time while exhibiting suitable characteristics as a sealing material has been found. It was the current situation.

Further, even the tube material made of the thermoplastic elastomer composition disclosed in Patent Document 6 does not always satisfy various properties such as flexibility and non-contamination (oil bleed).
JP 55-158621 A Japanese Patent Laid-Open No. 1-114030 Japanese Patent No. 3682786 JP 2004-165259 A JP 2001-316383 A JP 2004-142364 A

  The present invention has been made in view of such problems of the prior art, and the problem is that it is recyclable and has strength, flexibility, solvent resistance, gas permeability resistance, and Thermoplastic elastomer composition for sealing material capable of producing a sealing material excellent in sealing performance, recyclable molded member excellent in strength, flexibility, solvent resistance, gas permeation resistance, and sealing performance Another object of the present invention is to provide a capacitor that is small in size and excellent in airtightness and can be used for a long period of time.

  As a result of intensive studies to achieve the above-mentioned problems, the present inventors dynamically crosslinked a raw material composition containing a specific rubber component, a thermoplastic resin component, and an inorganic compound by crosslinking, and a plasticizer and a softener. It has been found that the above-mentioned problems can be achieved by not containing substantially the present invention, and the present invention has been completed.

  That is, according to the present invention, the following thermoplastic elastomer composition for sealing material, molded member, and capacitor are provided.

  [1] (A) at least one rubber component selected from the group consisting of ethylene / α-olefin copolymer rubber and isobutylene-isoprene copolymer rubber, and (B) α-olefin crystalline thermoplastic resin, an (A) rubber component, comprising at least one thermoplastic resin component selected from the group consisting of an α-olefin-based amorphous thermoplastic resin and a cyclic olefin-based thermoplastic resin, and (C) an inorganic compound. And (B) a raw material composition in which the content of the rubber component (A) is 10 to 90% by mass with respect to a total of 100% by mass of the thermoplastic resin component (D) in the presence of a crosslinking agent. A thermoplastic elastomer composition for a sealing material, which is substantially heat-free and contains substantially no plasticizer and softener.

  [2] The thermoplastic elastomer composition for sealing materials according to [1], wherein the inorganic compound (C) is at least one selected from the group consisting of montmorillonite, mica, talc, clay, kaolin, and graphite.

  [3] Said [1] which further contains (E) 1-30 mass parts hydrogenated diene polymer with respect to a total of 100 mass parts of said (A) rubber component and said (B) thermoplastic resin component. ] Or the thermoplastic elastomer composition for sealing materials according to [2].

  [4] The thermoplastic elastomer composition for sealing materials according to any one of [1] to [3], wherein the (D) crosslinking agent is an organic peroxide and / or a phenolic crosslinking agent.

  [5] A molded member formed by molding the thermoplastic elastomer composition for a sealing material according to any one of [1] to [4].

  [6] The molded member according to [5], which is formed by injection molding the thermoplastic elastomer composition for a sealing material.

  [7] The molded member according to [5] or [6], which is a sealing material or a tube material.

  [8] The molded member according to any one of [5] to [7], which is for a capacitor, a battery, a toner case, an inkjet printer including an ink cartridge, a flat panel display, or a housing.

  [9] A container having a seal portion, wherein the seal portion is provided with a seal material made of the thermoplastic elastomer composition for seal materials according to any one of [1] to [4]. Constructed container.

  [10] The heat for the sealing material according to any one of [1] to [4], wherein the capacitor element, an exterior case that accommodates the capacitor element and having at least one opening, and the opening are sealed. A capacitor provided with a sealing material made of a plastic elastomer composition.

  The thermoplastic elastomer composition for a sealing material of the present invention is recyclable and has an effect that a sealing material excellent in strength, flexibility, solvent resistance, gas permeation resistance, and sealing properties can be produced. It is what you play.

  In addition, the molded member of the present invention is recyclable and has the effect of being excellent in strength, flexibility, solvent resistance, gas permeation resistance, and sealing properties.

  The capacitor of the present invention is small in size and excellent in airtightness, and has an effect that it can be used for a long time.

  BEST MODE FOR CARRYING OUT THE INVENTION The best mode for carrying out the present invention will be described below, but the present invention is not limited to the following embodiment, and is based on the ordinary knowledge of those skilled in the art without departing from the gist of the present invention. It should be understood that modifications and improvements as appropriate to the following embodiments also fall within the scope of the present invention.

1. Thermoplastic elastomer composition for seal material One embodiment of the thermoplastic elastomer composition for seal material of the present invention is selected from the group consisting of (A) ethylene / α-olefin copolymer rubber and isobutylene-isoprene copolymer rubber At least one rubber component (hereinafter also referred to as “component (A)”), (B) α-olefin-based crystalline thermoplastic resin, α-olefin-based amorphous thermoplastic resin, and cyclic olefin-based heat And at least one thermoplastic resin component selected from the group consisting of plastic resins (hereinafter also referred to as “component (B)”) and (C) an inorganic compound (hereinafter also referred to as “component (C)”). The raw material composition in which the content ratio of the component (A) is 10 to 90% by mass with respect to the total of 100% by mass of the component (A) and the component (B) is (D) a crosslinking agent (hereinafter referred to as “(D) Ingredients "and In the presence of a plasticizer and a softening agent. The details will be described below.

((A) rubber component)
(A) component which comprises the thermoplastic elastomer composition for sealing materials of this embodiment is at least 1 type of rubber component selected from the group which consists of ethylene-alpha-olefin type | system | group copolymer rubber and isobutylene-isoprene copolymer rubber It is.

(Ethylene / α-olefin copolymer rubber)
The ethylene / α-olefin copolymer rubber is not particularly limited as long as it is a copolymer rubber containing a structural unit (a1) derived from ethylene and a structural unit (a2) derived from an α-olefin. Therefore, in the ethylene / α-olefin copolymer rubber, in addition to the binary copolymer containing the structural unit (a1) and the structural unit (a2), the structural unit (a3) derived from another monomer is used. Furthermore, a ternary copolymer may be included. Furthermore, as long as it contains the structural unit (a1) and the structural unit (a2), it may be a multi-component copolymer containing 4 or more different structural units. The ethylene / α-olefin copolymer rubber can be used alone or in combination of two or more.

  The proportion of the structural unit (a1) contained in the ethylene / α-olefin copolymer rubber is preferably 35 mol% or more when the total structural unit is 100 mol%. When the proportion of the structural unit (a1) is less than 35 mol%, the mechanical strength of the obtained sealing material tends to be insufficient. In addition, when there are too many ratios of a structural unit (a1), it exists in the tendency for the softness | flexibility of the sealing material obtained to become inadequate. Therefore, the proportion of the structural unit (a1) contained in the ethylene / α-olefin copolymer rubber is more preferably 40 to 90 mol%, when the total structural unit is 100 mol%, and is preferably 45 to 85 mol%. It is particularly preferred.

  Specific examples of the α-olefin constituting the structural unit (a2) include propylene, 1-butene, 2-butene, isobutene, 1-pentene, 2-methyl-1-butene, 2-methyl-2-butene, 3 -Methylbutene, 1-hexene, 4-methyl-1-pentene, 3-methyl-1-pentene, 1-heptene, 1-octene, 1-decene, 1-undecene and the like can be mentioned. Of these, propylene and 1-butene are preferable. These α-olefins can be used alone or in combination of two or more.

  The proportion of the structural unit (a2) contained in the ethylene / α-olefin copolymer rubber is preferably 5 to 65 mol%, and preferably 10 to 45 mol%, when all the structural units are 100 mol%. More preferably, it is 15-40 mol%, and it is especially preferable. When the proportion of the structural unit (a2) is less than 5 mol%, the resulting sealing material tends to hardly exhibit desired rubber elasticity. On the other hand, when the proportion of the structural unit (a2) is more than 65 mol%, the durability of the resulting sealing material tends to be lowered.

  When the ethylene / α-olefin copolymer rubber contains the structural unit (a3), examples of the monomer constituting the structural unit (a3) include non-conjugated diene compounds. Specific examples of the non-conjugated diene compound include linear acyclic diene compounds such as 1,4-hexadiene, 1,5-hexadiene, 1,6-hexadiene; 5-methyl-1,4-hexadiene, 3,7 -Branching of dimethyl-1,6-octadiene, 5,7-dimethylocta-1,6-diene, 3,7-dimethyl-1,7-octadiene, 7-methylocta-1,6-diene, dihydromyrcene, etc. Chain acyclic diene compounds; tetrahydroindene, methyltetrahydroindene, dicyclopentadiene, bicyclo [2.2.1] -hepta-2,5-diene, 5-methylene-2-norbornene, 5-ethylidene-2-norbornene , 5-propenyl-2-norbornene, 5-isopropylidene-2-norbornene, 5-cyclohexylidene-2-norbornene , It can be mentioned alicyclic diene compounds such as 5-vinyl-2-norbornene. Of these, 1,4-hexadiene, dicyclopentadiene, and 5-ethylidene-2-norbornene are preferable. These comparative conjugated diene compounds can be used singly or in combination of two or more.

  When the ethylene / α-olefin copolymer rubber contains the structural unit (a3), the proportion of the structural unit (a3) contained in the ethylene / α-olefin copolymer rubber is 100 mol% of all the structural units. When it is, it is preferable that it is 10 mol% or less, and it is still more preferable that it is 1-8 mol%. When the proportion of the structural unit (a3) is more than 10 mol%, the durability of the obtained sealing material tends to be lowered.

  The thermoplastic elastomer composition for a sealing material of the present embodiment exhibits excellent characteristics as a material for constituting the sealing material without using a raw material containing halogen. Therefore, when a capacitor is manufactured using the sealing material produced by the thermoplastic elastomer composition for sealing material of this embodiment that does not use halogen-containing raw materials, halogen does not elute into the electrolyte solution, and the capacitor characteristics deteriorate. There is an advantage that it becomes difficult to do.

  Further, as the ethylene / α-olefin copolymer rubber, a graft polymer obtained by polymerizing an unsaturated monomer to the ethylene / α-olefin copolymer rubber described so far can also be used. Examples of unsaturated monomers include vinyl acetate; (meth) acrylic acid; (meth) acrylic acid methyl, (meth) acrylic acid derivatives such as glycidyl (meth) acrylate, (meth) acrylamide; maleic acid; maleic anhydride, maleimide And maleic acid derivatives such as dimethyl maleate; conjugated diene compounds such as butadiene, isoprene and chloroprene.

  The crystallinity of the ethylene / α-olefin copolymer rubber by X-ray diffraction measurement is preferably 20% or less, and more preferably 15% or less. When the crystallinity of the ethylene / α-olefin copolymer rubber exceeds 20%, the flexibility of the obtained sealing material tends to be lowered.

  The iodine value of the ethylene / α-olefin copolymer rubber is preferably 5 to 30, and more preferably 7 to 20. When the iodine value of the ethylene / α-olefin copolymer rubber is less than 5, the crosslink density of the thermoplastic elastomer composition for a seal material is lowered, and the mechanical properties of the seal material tend to be lowered. On the other hand, when the iodine value of the ethylene / α-olefin copolymer rubber is more than 30, the crosslinking density of the thermoplastic elastomer composition for the sealing material is excessively increased, and the mechanical properties of the sealing material tend to be decreased. .

  In addition, oil-extended rubber (in which the mineral oil softener is added to the ethylene / α-olefin copolymer rubber described so far) contains mineral oil softener and is used in principle. It is not preferable to do. However, a small amount can be used as long as the effect of the present invention is not impaired.

  The intrinsic viscosity (measured in decalin solvent at 135 ° C.) of the ethylene / α-olefin copolymer rubber is preferably 1.8 dl / g or more. When the intrinsic viscosity of the ethylene / α-olefin copolymer rubber is less than 1.8 dl / g, mechanical strength and rubber elasticity tend to be lowered. On the other hand, if the intrinsic viscosity of the ethylene / α-olefin copolymer rubber is too large, the moldability tends to decrease. Therefore, the intrinsic viscosity of the ethylene / α-olefin copolymer rubber is more preferably 2.0 to 7.0 dl / g, and particularly preferably 2.0 to 6.0 dl / g.

(Isobutylene-isoprene copolymer rubber)
Isobutylene-isoprene copolymer rubber (hereinafter also referred to as “butyl rubber”) is a rubbery amorphous copolymer having a low degree of unsaturation, including a structural unit derived from isobutylene and a structural unit derived from isoprene. This isobutylene-isoprene copolymer rubber is obtained, for example, by slurry-polymerizing isobutylene and a small amount of isoprene in methyl chloride at a low temperature of about -100 ° C. using anhydrous aluminum chloride as a catalyst, and then drying. Can do.

  The proportion of the structural unit derived from isoprene contained in the isobutylene-isoprene copolymer rubber is preferably 0.5 to 15 mol% when the total structural unit is 100 mol%, and 0.8 to 5.0 mol. % Is more preferable. If the proportion of the structural unit derived from isoprene is less than 0.5 mol%, the crosslinking reaction tends to be delayed, and the mechanical strength may not be sufficient. On the other hand, when the proportion of the structural unit derived from isoprene is more than 15 mol%, the crosslinking density of the thermoplastic elastomer composition for a sealing material is excessively increased, and the mechanical properties of the sealing material tend to be decreased.

((B) thermoplastic resin component)
(B) component which comprises the thermoplastic elastomer composition for sealing materials of this embodiment is from (alpha) -olefin type | system | group crystalline thermoplastic resin, (alpha) -olefin type amorphous thermoplastic resin, and cyclic olefin type thermoplastic resin. And at least one thermoplastic resin component selected from the group consisting of:

(Α-olefin crystalline thermoplastic resin)
The α-olefin-based crystalline thermoplastic resin is a polymer containing a structural unit (b1) derived from an α-olefin. Further, the crystallinity of the α-olefin-based crystalline thermoplastic resin by X-ray diffraction is 50% or more, preferably 53% or more, and more preferably 55% or more. This crystallinity is closely related to the density. For example, when the α-olefin-based crystalline thermoplastic resin is polypropylene, the density of α-type crystals (monoclinic crystals) is 0.936 g / cm ³ , and the density of smectic crystallites (pseudo hexagonal crystals) is 0.886 g. / Cm ³ , and the density of the amorphous (atactic) component is 0.850 g / cm ³ . When the α-olefin-based crystalline thermoplastic resin is poly-1-butene, the density of the isotactic crystal component is 0.91 g / cm ³ and the density of the amorphous (atactic) component is 0.87 g / cm ³ . cm ³ .

Therefore, the density of the α- olefin crystalline thermoplastic resin, 0.89 g / cm ³ or more, preferably 0.90~0.94g / cm ^3. By setting the density to 0.89 g / cm ³ or more, the crystallinity can be set to 50% or more. In addition, when the crystallinity of the α-olefin-based crystalline thermoplastic resin is less than 50% and / or the density is less than 0.89 g / cm ³ , the heat resistance, mechanical strength, and the like of the obtained sealing material are increased. It tends to decrease.

  The α-olefin constituting the structural unit (b1) preferably has 2 to 12 carbon atoms. Of these, propylene and 1-butene are more preferable. The proportion of the structural unit (b1) contained in the α-olefin-based crystalline thermoplastic resin is preferably 80 mol% or more, more preferably 90 to 100 mol% when all the structural units are 100 mol%. preferable. If it is less than 80 mol%, the mechanical strength may not be sufficient.

  The α-olefin-based crystalline thermoplastic resin may be a copolymer containing a structural unit (b2) other than the structural unit (b1). This copolymer may be either a block copolymer or a random copolymer. However, in the case where the α-olefin-based crystalline thermoplastic resin is a block copolymer, the proportion of the structural unit (b2) is set so that the crystallinity of the block copolymer is 50% or more. When the unit is 100 mol%, it is preferably 40 mol% or less, and more preferably 20 mol% or less. In addition, this block copolymer can be manufactured by living polymerization using a Ziegler-Natta catalyst, for example.

  In addition, when the α-olefin-based crystalline thermoplastic resin is a random copolymer, the proportion of the structural unit (b2) is set so that the random copolymer has a crystallinity of 50% or more. When the unit is 100 mol%, it is preferably 15 mol% or less, more preferably 10 mol% or less. In addition, this random copolymer can be obtained by polymerizing α-olefin or the like in the presence of a catalyst component including a Ziegler-Natta catalyst, a soluble vanadium compound, an organoaluminum compound, and a solvent, for example. Examples of the polymerization method include a medium / low pressure method and the like, and it can be produced by a gas phase method (fluidized bed or stirred bed), a liquid phase method (slurry method or solution method) and the like. During polymerization, a molecular weight regulator such as hydrogen gas may be used as necessary.

As the soluble vanadium compound contained in the catalyst component, it is preferable to use a reaction product of VOCl ₃ and / or VCl ₄ and an alcohol. Examples of the alcohol include methanol, ethanol, n-propanol, isopropanol, n-butanol, sec-butanol, t-butanol, n-hexanol, n-octanol, 2-ethylhexanol, n-decanol, n-dodecanol and the like. Can do. Among these, C3-C8 alcohol is preferable.

  Examples of organoaluminum compounds contained in the catalyst component include triethylaluminum, triisobutylaluminum, tri-n-hexylaluminum, diethylaluminum monochloride, diisobutylaluminum monochloride, ethylaluminum sesquichloride, butylaluminum sesquichloride, ethylaluminum dichloride, butyl. Examples thereof include aluminum dichloride, methylaluminoxane which is a reaction product of trimethylaluminum and water. Of these, ethylaluminum sesquichloride, butylaluminum sesquichloride, a mixture of ethylaluminum sesquichloride and triisobutylaluminum, and a mixture of triisobutylaluminum and butylaluminum sesquichloride are preferred.

  The solvent contained in the catalyst component is preferably a hydrocarbon. Of these, n-pentane, n-hexane, n-heptane, n-octane, isooctane, and cyclohexane are more preferable. These solvents can be used alone or in combination of two or more.

  The maximum peak temperature (melting point) measured by the differential scanning calorimetry method of the α-olefin-based crystalline thermoplastic resin is preferably 100 ° C. or higher, and more preferably 120 ° C. or higher. When the melting point of the α-olefin-based crystalline thermoplastic resin is less than 100 ° C., the heat resistance and mechanical strength of the obtained sealing material tend to be insufficient.

  The melt flow rate (MFR) (temperature 230 ° C., load 2.16 kg) of the α-olefin-based crystalline thermoplastic resin is preferably 0.1 to 1000 g / 10 minutes, preferably 0.5 to 500 g / 10 minutes is more preferable, and 1 to 100 g / 10 minutes is particularly preferable. When the MFR of the α-olefin-based crystalline thermoplastic resin is less than 0.1 g / 10 minutes, the kneadability and extrusion processability of the raw material composition tend to be insufficient. On the other hand, when it exceeds 1000 g / 10 minutes, the mechanical strength of the obtained sealing material tends to be lowered.

Accordingly, the α-olefin-based crystalline thermoplastic resin has a crystallinity of 50% or more, a density of 0.89 g / cm ³ or more, a content of constituent units other than the constituent unit (b1) of 20 mol% or less, a melting point Is preferably 100 ° C. or higher and MFR of 0.1 to 100 g / 10 min. In particular, a copolymer of polypropylene and / or propylene and ethylene having a melting point of 140 to 170 ° C. is preferable. Two or more α-olefin crystalline thermoplastic resins may be used in combination.

  Specific examples of the α-olefin-based crystalline thermoplastic resin include polypropylene polymers, propylene / ethylene random polymers, propylene / ethylene block polymers and the like sold by Prime Polymer, Sun Allomer, and Nippon Polypro. Can be mentioned. More specifically, the product name “NOVATEC” (manufactured by Nippon Polypro Co., Ltd.), the product name “Wintech” (manufactured by Nippon Polypro Co., Ltd.), the product name “New Former” (manufactured by Nippon Polypro Co., Ltd.), and the product name “NEW TREN” "(Manufactured by Nippon Polypro Co., Ltd.), trade name" Newcon "(manufactured by Nippon Polypro Co., Ltd.), and the like.

(Α-olefin-based amorphous thermoplastic resin)
The α-olefin-based amorphous thermoplastic resin contains the structural unit (b3) derived from α-olefin, and the crystallinity by X-ray diffraction is less than 50%, preferably 30% or less, more preferably 20% or less. belongs to. Further, the density of the α- olefin amorphous thermoplastic resin is preferably from 0.85~0.89g / cm ^3, further preferably 0.85~0.88g / cm ^3.

  The α-olefin constituting the structural unit (b3) preferably has 3 or more carbon atoms, more preferably 3 to 12 carbon atoms. The proportion of the structural unit (b3) contained in the α-olefin-based amorphous thermoplastic resin is preferably 60 mol% or more when the total structural unit is 100 mol%. If it is less than 60 mol%, the mechanical strength may not be sufficient.

  Specific examples of the α-olefin-based amorphous thermoplastic resin include homopolymers such as atactic polypropylene and atactic poly 1-butene; more than 50 mol% of propylene and other α-olefins (ethylene, 1-butene). , 1-pentene, 1-hexene, 4-methyl-1-pentene, 1-octene, 1-decene, etc.); more than 50 mol% of 1-butene and other α-olefins (ethylene, And propylene, 1-pentene, 1-hexene, 4-methyl-1-pentene, 1-octene, 1-decene, and the like. Among these, atactic polypropylene, a copolymer composed of more than 50 mol% propylene and ethylene, and a copolymer composed of more than 50 mol% propylene and 1-butene are particularly preferable.

  Atactic polypropylene and atactic poly-1-butene can be produced by a polymerization method using a zirconocene compound-methylaluminoxane catalyst. In addition, atactic polypropylene can also be obtained as a by-product of polypropylene exemplified as the aforementioned α-olefin-based crystalline thermoplastic resin.

  When the α-olefin-based amorphous thermoplastic resin is a copolymer, this copolymer may be either a block copolymer or a random copolymer. However, when the α-olefin-based amorphous thermoplastic resin is a block copolymer, the proportion of the structural unit (b3) contained in the block copolymer is 60 when all the structural units are 100 mol%. It is preferable that it is -100 mol% or more. If it is less than 60 mol%, the mechanical strength may not be sufficient.

  The α-olefin-based amorphous thermoplastic resin has a polystyrene-equivalent number average molecular weight (Mn) by GPC of preferably 1000 to 20000, and more preferably 1500 to 15000. When Mn of the α-olefin-based amorphous thermoplastic resin is less than 1000, physical properties tend to be inferior. On the other hand, when Mn exceeds 20000, the kneadability and extrusion processability of the raw material composition tend to be insufficient. Two or more α-olefin-based amorphous thermoplastic resins can be used in combination.

  Examples of commercially available products of the α-olefin-based amorphous thermoplastic resin include a trade name “Best Plast” (manufactured by Degussa), a trade name “APAO” (manufactured by Huntsman), and the like.

(Cyclic olefin thermoplastic resin)
Specific examples of the cyclic olefin thermoplastic resin include cyclic olefin (co) polymers represented by the following general formula (1).

In the general formula (1), R ^{1 to} R ⁴ are each independently a hydrogen atom, a halogen atom, or a monovalent organic group, and R ¹ and R ² , and R ³ and R ⁴ are either May be integrated to form a divalent organic group. R ¹ and R ² , and R ³ and R ⁴ may be bonded to each other to form a monocyclic structure or a polycyclic structure. m is 0 or a positive integer, and p is 0 or a positive integer.

  More specific cyclic olefin-based thermoplastic resins include any of the (co) polymers (i) to (vii) shown below.

(I) A ring-opening polymer of a cyclic olefin represented by the general formula (1).
(Ii) A ring-opening copolymer of the cyclic olefin represented by the general formula (1) and a copolymerizable monomer.
(Iii) Hydrogenated (co) polymer of the ring-opening (co) polymer of (i) or (ii).
(Iv) A (co) polymer obtained by cyclization of the ring-opening (co) polymer of (i) or (ii) by Friedel-Craft reaction and hydrogenation.
(V) A saturated copolymer of the cyclic olefin represented by the general formula (1) and an unsaturated double bond-containing compound.
(Vi) an addition type (co) polymer of the cyclic olefin represented by the general formula (1), a vinyl cyclic hydrocarbon monomer and / or a cyclopentadiene monomer, and hydrogenation thereof ( Co) polymer.
(Vii) An alternating copolymer of a cyclic olefin represented by the general formula (1) and an acrylate.

(Cyclic olefin)
Examples of the monovalent organic group in the general formula (1) include C1-C30 hydrocarbon groups and monovalent polar groups other than hydrocarbon groups. Examples of the monovalent polar group include a carboxyl group, a hydroxyl group, an alkoxycarbonyl group, an allyloxycarbonyl group, an amino group, an amide group, and a cyano group. These polar groups may be bonded via a linking group such as a methylene group. In addition, a hydrocarbon group bonded through a linking group composed of a divalent organic group having a polarity such as a carbonyl group, an ether group, a silyl ether group, a thioether group, or an imino group should also be mentioned as a specific example of the polar group. Can do. Of these polar groups, a carboxyl group, a hydroxyl group, an alkoxycarbonyl group, and an allyloxycarbonyl group are preferable, and an alkoxycarbonyl group and an allyloxycarbonyl group are particularly preferable. The cyclic olefin represented by the general formula (1) may be used alone or in combination of two or more.

  Examples of the cyclic olefin represented by the general formula (1) include the following compounds. The cyclic olefin is not limited to these compounds.

Bicyclo [2.2.1] hept-2-ene, tricyclo [4.3.0.1 ^2,5 ] -8-decene, tricyclo [4.4.0.1 ^2,5 ] -3-undecene, Tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, pentacyclo [6.5.1.1 ^3,6 . 0 ^2,7 . 0 ^9,13 ] -4-pentadecene, 5-methylbicyclo [2.2.1] hept-2-ene, 5-ethylbicyclo [2.2.1] hept-2-ene, 5-methoxycarbonylbicyclo [ 2.2.1] Hept-2-ene, 5-methyl-5-methoxycarbonylbicyclo [2.2.1] hept-2-ene, 5-cyanobicyclo [2.2.1] hept-2-ene , 8-methoxycarbonyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-ethoxycarbonyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-n-propoxycarbonyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-isopropoxycarbonyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-n-butoxycarbonyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-methyl-8-methoxycarbonyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-methyl-8-ethoxycarbonyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-methyl-8-n-propoxycarbonyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-methyl-8-isopropoxycarbonyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-methyl-8-n-butoxycarbonyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 5-ethylidenebicyclo [2.2.1] hept-2-ene, 8-ethylidenetetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 5-phenylbicyclo [2.2.1] hept-2-ene, 8-phenyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 5-fluorobicyclo [2.2.1] hept-2-ene, 5-fluoromethylbicyclo [2.2.1] hept-2-ene, 5-trifluoromethyl Bicyclo [2.2.1] hept-2-ene, 5-pentafluoroethylbicyclo [2.2.1] hept-2-ene, 5,5-difluorobicyclo [2.2.1] hept-2- Ene, 5,6-difluorobicyclo [2.2.1] hept-2-ene, 5,5-bis (trifluoromethyl) bicyclo [2.2.1] hept-2-ene, 5,6-bis (Trifluoromethyl) bicyclo [2.2.1] hept-2-ene, 5-methyl-5-trifluoromethylbicyclo [2.2.1] hept-2-ene, 5,5,6-trifluoro Bicyclo [2.2.1] hept-2-ene 5,5,6-tris (fluoromethyl) bicyclo [2.2.1] hept-2-ene, 5,5,6,6-tetrafluorobicyclo [2.2.1] hept-2-ene, 5 , 5,6,6-tetrakis (trifluoromethyl) bicyclo [2.2.1] hept-2-ene, 5,5-difluoro-6,6-bis (trifluoromethyl) bicyclo [2.2.1]. ] Hept-2-ene, 5,6-difluoro-5,6-bis (trifluoromethyl) bicyclo [2.2.1] hept-2-ene, 5,5,6-trifluoro-5-trifluoro Methylbicyclo [2.2.1] hept-2-ene, 5-fluoro-5-pentafluoroethyl-6,6-bis (trifluoromethyl) bicyclo [2.2.1] hept-2-ene, 5 , 6-Difluoro-5-heptafluoro-i so-propyl-6-trifluoromethylbicyclo [2.2.1] hept-2-ene, 5-chloro-5,6,6-trifluorobicyclo [2.2.1] hept-2-ene, 5 , 6-dichloro-5,6-bis (trifluoromethyl) bicyclo [2.2.1] hept-2-ene, 5,5,6-trifluoro-6-trifluoromethoxybicyclo [2.2.1]. ] Hept-2-ene, 5,5,6-trifluoro-6-heptafluoropropoxybicyclo [2.2.1] hept-2-ene, 8-fluorotetracyclo [4.4.0.1 ^{2, 5} . 1 ^7,10 ] -3-dodecene, 8-fluoromethyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-difluoromethyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-trifluoromethyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-pentafluoroethyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,8-difluorotetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,9-difluorotetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,8-bis (trifluoromethyl) tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,9-bis (trifluoromethyl) tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-methyl-8-trifluoromethyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,8,9-trifluorotetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,8,9-tris (trifluoromethyl) tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,8,9,9-tetrafluorotetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,8,9,9-tetrakis (trifluoromethyl) tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,8-difluoro-9,9-bis (trifluoromethyl) tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,9-difluoro-8,9-bis (trifluoromethyl) tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,8,9-trifluoro-9-trifluoromethyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,8,9-trifluoro-9-trifluoromethoxytetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,8,9-trifluoro-9-pentafluoropropoxytetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-fluoro-8-pentafluoroethyl-9,9-bis (trifluoromethyl) tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,9-difluoro-8-heptafluoroiso-propyl-9-trifluoromethyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-chloro-8,9,9-trifluorotetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8,9-dichloro-8,9-bis (trifluoromethyl) tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8- (2,2,2-trifluoroethoxycarbonyl) tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene, 8-methyl-8- (2,2,2-trifluoroethoxycarbonyl) tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] -3-dodecene.

In the general formula (1), R ¹ and R ³ are preferably each independently a hydrogen atom or a hydrocarbon group. The number of carbon atoms of the hydrocarbon machine is preferably 1 to 10, more preferably 1 to 4, and particularly preferably 1 or 2. R ¹ and R ³ are particularly preferably an alkyl group, and most preferably a methyl group.

In the general formula (1), R ² and R ⁴ are each independently a hydrogen atom or a monovalent organic group, and at least one of R ² and R ⁴ is a hydrogen atom. Or the monovalent polar group.

  In the general formula (1), m is preferably an integer of 0 to 3, and p is preferably an integer of 0 to 3. The value of m + p is preferably 0 to 4, more preferably 0 to 2, and particularly preferably m = 1 and p = 0. Cyclic olefins with m = 1 and p = 0 are most preferred in that a cyclic olefin-based thermoplastic resin having a high glass transition temperature and excellent mechanical strength can be obtained.

Furthermore, the cyclic olefin in which at least one of R ² and R ⁴ is a polar group represented by the following general formula (2) has a high glass transition temperature, low hygroscopicity, and excellent adhesion to various materials. It is preferable at the point from which the cyclic olefin type thermoplastic resin which has this is obtained.
_{- (CH 2) n COOR (} 2)

In the general formula (2), R is a hydrocarbon group. The number of carbon atoms in R is preferably 1 to 12, more preferably 1 to 4, and particularly preferably 1 or 2. R is preferably an alkyl group. Moreover, in said general formula (2), n is an integer of 0-5. A cyclic olefin having a smaller value of n is preferable because a cyclic olefin-based thermoplastic resin having a high glass transition temperature can be obtained, and a cyclic olefin having n = 0 is particularly preferable in terms of easy synthesis. In particular, the polar group represented by the general formula (2) is bonded to the carbon atom to which R ¹ and R ³ which are alkyl groups are bonded, so that the cyclic olefin-based thermoplastic resin having low hygroscopicity. Is preferable in that it is obtained.

  The (i) ring-opening polymer can be obtained by ring-opening polymerization of the aforementioned cyclic olefin in the presence of a metathesis catalyst. The (ii) ring-opening copolymer can be obtained by ring-opening copolymerization of the above-mentioned cyclic olefin and a copolymerizable monomer.

  (Ii) Examples of the copolymerizable monomer used for obtaining the ring-opening copolymer include cycloolefin. The cycloolefin has preferably 4 to 20 carbon atoms, more preferably 5 to 12 carbon atoms. More specific examples of the copolymerizable monomer include cyclobutene, cyclopentene, cycloheptene, cyclooctene, dicyclopentadiene and the like. These cycloolefins may be used individually by 1 type, or may use 2 or more types together. In addition, as a commercial item of cyclic olefin type thermoplastic resin, brand name “ARTON” (manufactured by JSR), brand name “TOPAS” (manufactured by Ticona, Germany), brand name “Apel” (manufactured by Mitsui Chemicals), commodity The name “Zeonex” (manufactured by Nippon Zeon Co., Ltd.) and the product name “Zeonoa” (manufactured by Nippon Zeon Co., Ltd.) can be exemplified.

(Ratio of rubber component and thermoplastic resin component)
The content ratio of the component (A) in the thermoplastic elastomer composition for sealing material of the present embodiment is 10 to 90% by mass, when the total amount of the component (A) and the component (B) is 100% by mass, Preferably it is 15-85 mass%, More preferably, it is 20-85 mass%. When the content ratio of the component (A) is less than 10% by mass, the flexibility and rubber elasticity of the resulting thermoplastic elastomer composition for sealing material are lowered. On the other hand, when the content ratio of the component (A) is more than 90% by mass, the phase structure (morphology) of the thermoplastic elastomer composition for sealing material obtained is a characteristic that is a characteristic of the dynamically crosslinked thermoplastic elastomer composition The sea-island structure (the thermoplastic resin is the sea (matrix) and the crosslinked rubber particles are islands (domains)) is hardly formed, and the fluidity and moldability are lowered.

((C) inorganic compound)
(C) component contained in the thermoplastic elastomer composition for sealing materials of this embodiment is an inorganic compound. By containing this (C) component, the gas-permeation resistance of the sealing material obtained using the thermoplastic elastomer composition for sealing materials of this embodiment can be made extremely excellent.

  Although the kind of (C) component which can be contained is not specifically limited, Specifically, it is a smectite clay compound, such as montmorillonite, saponite, bentonite, hectorite, beidellite, stevensite, and nontronite. Examples obtained by organically modifying these smectite clay compounds; layered clay compounds such as vermiculite, halloysite, kaolinite, and swellable mica; talc; clay and the like can be given as preferred examples. These inorganic compounds may be natural products or synthetic products. Moreover, it is also preferable to use the baked inorganic compound which baked these inorganic compounds and removed the impurity according to the use of the thermoplastic elastomer composition for sealing materials of this embodiment. In addition, these inorganic compounds can be used individually by 1 type or in combination of 2 or more types.

  There is no restriction | limiting in particular also about the shape of (C) component, For example, (C) components, such as fiber shape, flake shape, spherical shape, rod shape, needle shape, hollow shape, can be used. However, in order to suppress the influence on physical properties when dispersed in the thermoplastic elastomer composition as much as possible, and to improve the effect of effectively preventing the diffusion of gas molecules inside the thermoplastic elastomer composition, It is preferable to use a (C) component in the form of a plate or plate.

  When the shape of the component (C) is flaky or plate-like, the aspect ratio of the flaky or plate-like (C) component is preferably 1.5 to 50, and preferably 2 to 30. Is more preferable, and 2 to 15 is particularly preferable. When the aspect ratio is less than 1.5, the effect on gas permeability resistance tends to be small. On the other hand, when the aspect ratio is more than 50, the maximum length of the component (C) becomes excessive and the strength tends to decrease. The “aspect ratio” in the present specification refers to a value obtained by dividing the maximum length in the surface direction of the inorganic compound by the minimum length (= maximum length / minimum length).

  When the shape of the component (C) is flaky or plate-like, the maximum length of the flaky or plate-like (C) component is 0.1 to 50 μm in the thermoplastic elastomer composition. This is preferable because it is possible to suppress the influence on physical properties when dispersed as much as possible and to improve the effect of effectively preventing the diffusion of gas molecules inside the thermoplastic elastomer composition. In order to further suppress the influence on physical properties when dispersed in the thermoplastic elastomer composition, and to further improve the effect of effectively preventing gas molecule diffusion inside the thermoplastic elastomer composition, The maximum length of the flaky or plate-like (C) component is more preferably 0.5 to 30 μm, and particularly preferably 1 to 15 μm.

  The content ratio of the component (C) is preferably 5 to 200 parts by mass, more preferably 10 to 100 parts by mass, with respect to 100 parts by mass in total of the components (A) and (B). More preferably, it is 10-50 mass parts. If the amount is less than 5 parts by mass, the improvement in gas permeability resistance may be insufficient. On the other hand, if it exceeds 200 parts by mass, rubber elasticity tends to be lost.

((D) Crosslinking agent)
(D) component used in order to manufacture the thermoplastic elastomer composition for sealing materials of this embodiment is a crosslinking agent. (D) The kind of component is not specifically limited. However, the compound is preferably a compound capable of crosslinking at least the component (A) by dynamic heat treatment at a temperature equal to or higher than the melting point of the component (B).

  Specific examples of the component (D) include organic peroxides, phenol resin crosslinking agents, sulfur, sulfur compounds, p-quinones, p-quinone dioxime derivatives, bismaleimide compounds, epoxy compounds, silane compounds, amino resins, Examples include polyol cross-linking agents, polyamines, triazine compounds, and metal soaps. Of these, organic peroxides and phenol resin crosslinking agents are preferred. These can be used individually by 1 type or in combination of 2 or more types.

  Examples of the organic peroxide include 1,3-bis (t-butylperoxyisopropyl) benzene, 2,5-dimethyl-2,5-bis (t-butylperoxy) hexyne-3, 2,5-dimethyl- 2,5-bis (t-butylperoxy) hexene-3,2,5-dimethyl-2,5-bis (t-butylperoxy) hexane, 2,2'-bis (t-butylperoxy)- p-isopropylbenzene, dicumyl peroxide, di-t-butyl peroxide, t-butyl peroxide, p-menthane peroxide, 1,1-bis (t-butylperoxy) -3,3,5-trimethyl Cyclohexane, dilauroyl peroxide, diacetyl peroxide, t-butyl peroxybenzoate, 2,4-dichlorobenzoyl peroxide, p-chlorobenzoyl Okishido, benzoyl peroxide, may be mentioned di (t-butylperoxy) perbenzoate, n- butyl-4,4-bis (t-butylperoxy) valerate, and t-butyl peroxy isopropyl carbonate. Among them, 1,3-bis (t-butylperoxyisopropyl) benzene, 2,5-dimethyl-2,5-di (t-butylperoxy) hexyne-3, 2,5-dimethyl-2,5- Di (t-butylperoxy) hexane, α, α-bis (t-butylperoxy) diisopropylbenzene, dicumyl peroxide, and di-t-butyl peroxide are preferred. These can be used individually by 1 type or in combination of 2 or more types.

  Examples of the phenol resin crosslinking agent include p-substituted phenol compounds represented by the following general formula (3), o-substituted phenol / aldehyde condensate, m-substituted phenol / aldehyde condensate, brominated alkylphenol / aldehyde condensate. And the like. Of these, p-substituted phenolic compounds are preferred. These can be used individually by 1 type or in combination of 2 or more types.

  In said general formula (3), R is a C1-C15 saturated hydrocarbon group, n is an integer of 0-10. The p-substituted phenol compound can be obtained by a condensation reaction between a p-substituted phenol and an aldehyde (preferably formaldehyde) in the presence of an alkali catalyst.

  Commercially available phenolic crosslinking agents include trade name “Tacicol 201” (alkylphenol formaldehyde resin, manufactured by Taoka Chemical Co., Ltd.), product name “Tacicol 250-I” (brominated alkylphenol formaldehyde resin having a bromination rate of 4%, Taoka Chemical Industry Co., Ltd.), trade name “Tactrol 250-III” (brominated alkylphenol formaldehyde resin, manufactured by Taoka Chemical Industries), trade name “PR-4507” (manufactured by Gunei Chemical Industry Co., Ltd.), trade name “ST137X” Rohm & Haas), trade name "Sumilite Resin PR-22193" (Sumitomo Durez), trade name "Tamanor 531" (Arakawa Chemical Co., Ltd.), trade name "SP1059", trade name "SP1045", product Name “SP1055”, product name “SP1056” (manufactured by Schenectady), It can be cited name "CRM-0803" (manufactured by Showa Union Gosei Co.). Among these, “Tack roll 201” is preferably used.

  The amount of the crosslinking agent used is 0.01 to 20 mass with respect to 100 mass parts in total of the component (A) and the component (B) contained in the raw material composition for producing the thermoplastic elastomer composition for sealing material. Part, preferably 0.1 to 15 parts by weight, more preferably 1 to 10 parts by weight.

  In the case where an organic peroxide is used as the crosslinking agent, the amount of the organic peroxide used is the component (A) and the component (B) contained in the raw material composition for producing the thermoplastic elastomer composition for sealing material. It is preferable to set it as 0.05-10 mass parts with respect to a total of 100 mass parts of a component, and it is still more preferable to set it as 0.1-5 mass parts. When the amount of the organic peroxide used exceeds 10 parts by mass, the degree of crosslinking becomes excessively high, the molding processability decreases, and the mechanical properties of the resulting thermoplastic elastomer composition for sealing materials tend to decrease. is there. On the other hand, when the amount of the organic peroxide used is less than 0.05 parts by mass, the degree of crosslinking is insufficient, and the rubber elasticity and mechanical strength of the resulting thermoplastic elastomer composition for sealing material tend to be reduced.

  Moreover, when using a phenol resin crosslinking agent as a crosslinking agent, the usage-amount of this phenol resin crosslinking agent is the (A) component contained in the raw material composition for manufacturing the thermoplastic elastomer composition for sealing materials ( It is preferable to set it as 0.2-10 mass parts with respect to a total of 100 mass parts of B) component, and it is still more preferable to set it as 0.5-5 mass parts. If the amount of the phenol resin crosslinking agent used exceeds 10 parts by mass, the moldability tends to be lowered. On the other hand, when the amount of the phenol resin cross-linking agent used is less than 0.2, the degree of cross-linking is insufficient, and the rubber elasticity and mechanical strength of the resulting thermoplastic elastomer composition for sealing material tend to decrease.

  It is preferable to use a crosslinking aid and / or a crosslinking accelerator together with the crosslinking agent because the crosslinking reaction can be performed gently and uniform crosslinking can be formed. When organic peroxide is used as a crosslinking agent, sulfur, sulfur compounds (powder sulfur, colloidal sulfur, precipitated sulfur, insoluble sulfur, surface-treated sulfur, dipentamethylene thiuram tetrasulfide, etc.), oxime compounds are used as crosslinking aids. (P-quinone oxime, p, p′-dibenzoylquinone oxime, etc.), polyfunctional monomers (ethylene glycol di (meth) acrylate, diethylene glycol di (meth) acrylate, triethylene glycol di (meth) acrylate, tetraethylene) Glycol di (meth) acrylate, polyethylene glycol di (meth) acrylate, trimethylolpropane tri (meth) acrylate, diallyl phthalate, tetraallyloxyethane, triallyl cyanurate, N, N′-m-phenylenebismaleimide, N N'- toluylene bismaleimide, maleic anhydride, divinylbenzene, the use of di (meth) zinc acrylate and the like) or the like. Of these, p, p'-dibenzoylquinone oxime, N, N'-m-phenylenebismaleimide, and divinylbenzene are preferable. These can be used individually by 1 type or in combination of 2 or more types. Note that N, N′-m-phenylenebismaleimide exhibits an action as a crosslinking agent, and therefore can be used alone as a crosslinking agent.

  In the case of using an organic peroxide as a crosslinking agent, the amount of crosslinking aid used is 10 parts by mass or less with respect to 100 parts by mass in total of the component (A) and the component (B) contained in the raw material composition It is preferable to carry out, and it is still more preferable to set it as 0.2-5 mass parts. When the amount of the crosslinking aid used exceeds 10 parts by mass, the degree of crosslinking becomes excessively high, the molding processability is lowered, and the mechanical properties of the resulting thermoplastic elastomer composition for sealing material tend to be lowered. .

((E) Hydrogenated diene polymer)
The thermoplastic elastomer composition for sealing materials of this embodiment preferably further contains (E) a hydrogenated diene polymer (hereinafter also referred to as “component (E)”). The component (E) may be any component obtained by hydrogenating a polymer of a conjugated diene, but in addition to this, a random copolymer of a conjugated diene and an aromatic vinyl compound, or the following (e) to (i A hydrogenated block copolymer containing two or more polymer blocks selected from the polymer blocks shown in (1) is preferred.

(E) Aromatic vinyl compound polymer block in which the proportion of aromatic vinyl compound units is 80% by mass or more (f) Conjugated diene polymer block in which the proportion of conjugated diene units is 80% by mass or more (g) 1, 2 Conjugated diene polymer block in which the total of-and 3,4-bond content is less than 25% by mass (h) The total of 1,2- and 3,4-bond content is 25% by mass or more and 90% by mass or less Conjugated diene polymer block (i) Random copolymer block of aromatic vinyl compound and conjugated diene

  The random copolymer block shown in the above (i) includes a so-called taper type in which the content of the aromatic vinyl compound unit continuously changes in one molecule. Examples of the “block copolymer containing two or more polymer blocks selected from the polymer blocks shown in (e) to (i)” include (e)-(f), (e)- (G), (e)-(h), (e)-(i), (g)-(h), (g)-(i), [(e)-(f)] xY, [ (E)-(g)] xY, [(e)-(h)] xY, [(e)-(i)] xY, [(g)-(h)] xY , [(G)-(i)] x-Y, (e)-(f)-(g), (e)-(f)-(i), (e)-(f)-(e), (E)-(g)-(e), (e)-(h)-(e), (e)-(h)-(g), (e)-(i)-(e), [( e)-(f)-(g)] xY, [(e)-(f)-(i)] xY, [(e)-(f)-(e)] xY, [ (E)-(g)-(e) x-Y, [(e)-(h)-(e)] x-Y, [(e)-(h)-(g)] x-Y, [(e)-(i)-(e) ] X-Y, (e)-(f)-(e)-(f), (f)-(e)-(f)-(e), (e)-(g)-(e)-( g), (g)-(e)-(g)-(e), [(e)-(f)-(e)-(f)] x-Y, (e)-(f)-(e )-(F)-(e), [(e)-(f)-(e)-(f)-(e)] xY, [(f)-(e)] xY, [( g)-(e)] x-Y, [(h)-(e)] x-Y, [(i)-(e)] x-Y, (f)-(e)-(f)-( g), (f)-(e)-(f)-(i), (f)-(e)-(f)-(e), (f)-(e)-(g)-(e) , (G)-(e)-(h)-(e), (g)-(e)-(h)-(g) (G)-(e)-(i)-(e), [(g)-(e)-(f)-(g)] x-Y, [(h)-(e)-(f)- (I)] x-Y, [(h)-(e)-(f)-(e)] x-Y, [(h)-(e)-(g)-(e)] x-Y, [(H)-(e)-(h)-(e)] xY, [(h)-(e)-(h)-(g)] xY, [(h)-(e) -(I)-(e)] x-Y, (h)-(e)-(f)-(e)-(f), (h)-(f)-(e)-(f)-( e), (h)-(e)-(g)-(e)-(g), (h)-(g)-(e)-(g)-(e), [(h)-(e )-(F)-(e)-(f)] x-Y, (h)-(e)-(f)-(e)-(e)-(e), [(h)-(e) -(F)-(e)-(f)-(e)] x-Y, etc. X ≧ 2 and Y is the residue of the coupling agent).

  In addition, when making the shape of the hydrogenated diene polymer obtained into a pellet shape, (e) a polymer block and / or (g) a polymer block is included as a block component outside the hydrogenated modified polymer. It is preferable.

  Examples of the aromatic vinyl compound used to produce the component (E) include styrene, α-methylstyrene, p-methylstyrene, t-butylstyrene, divinylbenzene, N, N-dimethyl-p-aminoethylstyrene, 2,4-dimethylstyrene, N, N-diethyl-p-aminoethylstyrene, 2,4-dimethylstyrene, vinylnaphthalene, vinylanthracene and the like can be mentioned. Of these, styrene and α-methylstyrene are preferable.

  The conjugated diene used to produce the component (E) is 1,3-butadiene, isoprene, 2,3-dimethyl-1,3-butadiene, 1,3-pentadiene, 2-methyl-1, Examples include 3-pentadiene, 1,3-hexadiene, 4,5-dimethyl-1,3-octadiene, and chloroprene. Of these, 1,3-butadiene and isoprene are preferable.

  The composition ratio of the conjugated diene monomer and the aromatic vinyl monomer (conjugated diene compound / aromatic vinyl compound (mass ratio)) constituting the pre-hydrogenated polymer is not particularly limited, but is usually a conjugated diene. / Aromatic vinyl compound = 5/95 to 100/0, preferably conjugated diene / aromatic vinyl compound = 5/95 to 95/5, more preferably conjugated diene / aromatic vinyl compound = 30/70 to 92/8 It is.

  Component (E) is preferably one in which 80% or more of the double bonds derived from the conjugated diene contained in the pre-hydrogenation polymer are saturated, and preferably 90% or more is saturated. . When the saturation ratio is less than 80%, the weather resistance and the like may decrease. Moreover, it is preferable that the weight average molecular weights of (E) component are 5000-1 million, and it is still more preferable that it is 10000-500000.

  As said coupling agent, a halogen compound, an epoxy compound, a carbonyl compound, a polyvinyl compound etc. can be mentioned, for example. More specifically, for example, methyldichlorosilane, methyltrichlorosilane, butyltrichlorosilane, tetrachlorosilane, dibromoethane, epoxidized soybean oil, divinylbenzene, tetrachlorotin, butyltrichlorotin, tetrachlorogermanium, bis (trichlorosilyl) ) Ethane, diethyl adipate, dimethyl adipate, dimethyl terephthalic acid, diethyl terephthalic acid, polyisocyanate and the like.

  In the method for producing component (E), the microstructure, that is, the content of 1,2- or 3,4-bonds, can be controlled by using a Lewis base together with a hydrocarbon solvent. Examples of such Lewis bases include ethers and amines, and more specifically, diethyl ether, tetrahydrofuran, propyl ether, butyl ether, higher ethers, tetrahydrofurfuryl methyl ether, tetrahydrofurfuryl ethyl ether, 1 , 4-dioxane, bis (tetrahydrofurfuryl) formal, 2,2-bis (2-tetrahydrofurfuryl) propane, ethylene glycol dibutyl ether, diethylene glycol dimethyl ether, propylene glycol diethyl ether, and propylene glycol ethyl propyl ether Glycol ether derivatives; tertiary amines such as tetramethylethylenediamine, pyridine, tributylamine, etc.

  Specific examples of the component (E) include hydrogenated styrene-butadiene block copolymers, hydrogenated styrene-isoprene block copolymers, hydrogenated styrene-butadiene-isoprene block copolymers, hydrogenated butadiene block copolymers, and the like. Can be mentioned. Of these, hydrogenated styrene-butadiene block copolymers, hydrogenated styrene-butadiene-isoprene block copolymers, and hydrogenated butadiene block polymers are preferred. (E) Component commercial products include Kuraray Septon (trade name), Hibler (trade name), Asahi Kasei's Tuftec (trade name), JSR Dynalon (trade name), Kraton Polymers Clayton (trade name) and the like.

  The content ratio of the component (E) is preferably 1 to 30 parts by mass and more preferably 5 to 15 parts by mass with respect to 100 parts by mass of the total amount of the components (A) and (B). . When the amount is less than 1 part by mass, the flexibility of the thermoplastic elastomer composition for sealing material finally obtained tends to be lowered. On the other hand, if it exceeds 30 parts by mass, the heat resistance of the finally obtained thermoplastic elastomer composition for sealing material may be lowered.

(Additives, fillers)
Various additives and / or fillers can be contained in the thermoplastic elastomer composition for a sealing material of the present embodiment as long as the effects of the present invention are not impaired. Additives include anti-aging agents, antioxidants, UV absorbers, antistatic agents, weathering agents, non-halogen flame retardants, fillers, antibacterial and antifungal agents, blocking agents, sealability improvers, thermal stability And stabilizers such as an agent, a light stabilizer, a copper damage inhibitor, a metal deactivator, a crystal nucleating agent, a tackifier, a foaming aid, a colorant (dye, pigment, etc.), and the like.

  Further, in order to improve the sliding characteristics such as the wearability of the final product, a lubricant component can be added within a range not impairing the effects of the present invention. Examples of the lubricant component include metal soap, olefin resin wax, fatty acid, fatty acid amide, fatty alcohol, fatty acid ester and the like. In addition, the lubricant component is preferably a solid component or a compound exhibiting high viscosity characteristics at the normal use temperature of the final product. In the case of liquid or low-viscosity characteristics, defects such as thinning due to elution from the thermoplastic elastomer composition for sealing materials are likely to occur, and the sealing performance may not be maintained over a long period of time.

  Fillers include metal powders such as ferrite, inorganic fibers such as glass fibers and metal fibers, organic fibers such as carbon fibers and aramid fibers, composite fibers, inorganic whiskers such as potassium titanate whiskers, glass beads, and glass balloons. , Glass flakes, mica, calcium carbonate, talc, wet silica, dry silica, alumina, alumina silica, calcium silicate, hydrotalcite, kaolin, diatomaceous earth, graphite, pumice, evo powder, cotton flock, cork powder, sulfuric acid Examples thereof include barium, fluororesin, polymer beads, carbon black, cellulose powder, rubber powder, and wood powder.

(Other polymer components)
The thermoplastic elastomer composition for sealing materials of this embodiment contains other polymer components in addition to the component (A), the component (B), and the component (E) used as necessary. Also good. The kind of the other polymer component that can be contained is not particularly limited as long as it does not hinder the mechanical strength, flexibility, and the like of the thermoplastic elastomer composition for a sealing material to be obtained.

  Other polymer components include ionomer resin, aminoacrylamide polymer, polyethylene and its maleic anhydride graft polymer, polyisobutylene, ethylene / vinyl alcohol copolymer, ethylene / vinyl acetate copolymer, polyethylene oxide, ethylene Acrylic acid copolymer, polypropylene and its maleic anhydride graft polymer, polyisobutylene and its maleic anhydride graft polymer, chlorinated polypropylene, 4-methylpentene-1 resin, polystyrene, ABS resin, ACS resin, AS resin, AES resin, ASA resin, MBS resin, acrylic resin, methacrylic resin, polyamide resin, polycarbonate, vinyl alcohol resin, vinyl acetal resin, polyether resin, polyethylene terephthalate, ethylene -Olefin / non-conjugated diene copolymer rubber, nitrile rubber and hydrogenated products thereof, acrylic rubber, silicone rubber, butyl rubber, natural rubber, syndiotactic 1,2-polybutadiene, simple blend type olefin thermoplastic elastomer, implant type Examples thereof include olefin-based thermoplastic elastomers, dynamically crosslinked olefin-based thermoplastic elastomers, polyurethane-based thermoplastic elastomers, polyester-based thermoplastic elastomers, polyamide-based thermoplastic elastomers, and fluorine-based thermoplastic elastomers. These polymer components can be used singly or in combination of two or more.

(Thermoplastic elastomer composition for sealing material)
The thermoplastic elastomer composition for sealing materials of this embodiment contains substantially no plasticizer. Therefore, problems such as thinning of the meat due to volatilization of the plasticizer are not likely to occur, and excellent sealing properties are exhibited over a long period of time. Moreover, the thermoplastic elastomer composition for sealing materials of this embodiment does not contain a softener substantially. Therefore, since the sealing characteristics can be maintained for a long period of time, the loss of permeation of the encapsulated substance can be reduced. Here, “substantially free of” a plasticizer and a softener as referred to in the present specification means that the total content of the plasticizer and the softener is based on the entire thermoplastic elastomer composition for sealing material. 5.0 mass% or less, preferably 2.0 mass% or less, more preferably 1.0 mass% or less. In addition, the content ratio of the most preferable plasticizer and softener is 0.1% by mass or less (that is, it is not included at all).

  In addition, the thermoplastic elastomer composition for sealing materials of this embodiment can also contain a trace amount plasticizer in the range which does not impair the effect of this invention. Examples of the plasticizer that can be contained include phthalic acid esters such as dimethyl phthalate, diethyl phthalate, dibutyl phthalate, diisobutyl phthalate, dioctyl phthalate, butyl octyl phthalate, di- (2-ethylhexyl) phthalate, diisooctyl phthalate, and diisodecyl phthalate. Dimethyl adipate, diisobutyl adipate, di- (2-ethylhexyl) adipate, diisooctyl adipate, diisodecyl adipate, octyl decyl adipate, di- (2-ethylhexyl) azelate, diisooctyl azelate, diisobutyl azelate, dibutyl seba Fatty acid esters such as keto, di- (2-ethylhexyl) sebacate, diisooctyl sebacate; trimellitic acid isodecyl ester, In addition to trimellitic acid esters such as meritic acid octyl ester, trimellitic acid n-octyl ester, trimellitic acid isononyl ester, di- (2-ethylhexyl) fumarate, diethylene glycol monooleate, glyceryl monoricinoleate, trilauryl Mention may be made of phosphate, tristearyl phosphate, tri- (2-ethylhexyl) phosphate, tricresyl phosphate, epoxidized soybean oil, polyether ester and the like. On the other hand, as plasticizers and softeners that are not preferable to use, petroleum softeners such as aromatic oil, naphthenic oil, paraffin oil, white oil, petrolatum, gilsonite; castor oil, cottonseed oil, rapeseed oil, palm oil, coconut oil And vegetable oil-based softeners such as rosin.

  The melt flow rate (MFR) of the thermoplastic elastomer composition for sealing material of the present embodiment is preferably 0.1 g / 10 min or more under the conditions of a temperature of 230 ° C. and a load of 21 N, and 1.0 g / 10 min. More preferably, it is more preferably 2.0 g / 10 min or more, and most preferably 3.0 g / 10 min or more. If the MFR is less than 0.1 g / 10 min, the processability by various molding methods tends to be insufficient.

  The thermoplastic elastomer composition for a seal material of the present embodiment is excellent in fluidity. Therefore, even when various molded products are produced using a mold, mold contamination is unlikely to occur and the mold can be used for a long period of time. Moreover, since the thermoplastic elastomer composition for sealing materials of this embodiment is recyclable, the material can be used without waste.

(Method for producing thermoplastic elastomer composition for sealing material)
The thermoplastic elastomer composition for a seal material of the present embodiment is obtained by dynamically heat-treating a raw material composition containing the component (A), the component (B), and the component (C) with (D) a crosslinking agent. Can be manufactured by. Here, “dynamically heat-treating” refers to both applying a shearing force and heating. And the thermoplastic elastomer composition for sealing materials of this embodiment obtained by such dynamic heat treatment specifically has the component (B) as the sea phase, and the component (A) These particles constitute a so-called sea-island structure in which the particles are dispersed as island phases.

  In preparing the raw material composition, the component (A) and the component (B) may be used as they are, or those prepared as compositions containing the same or different additives may be used. The shape of the component (A) may be any of a veil shape, a crumb shape, a pellet shape, and a powder shape (including a crushed product of a bale rubber or a crumb rubber). Moreover, you may use combining several (A) component from which a shape differs.

  As a device used for “dynamic heat treatment”, a melt kneader or the like can be cited as a suitable example. The treatment by the melt kneader may be either a continuous type or a batch type. Specific examples of the melt kneader include an open type mixing roll, a non-open type Banbury mixer, a single screw extruder, a twin screw extruder, a continuous kneader, and a pressure kneader. Among these, it is preferable to use a continuous melt kneader such as a single screw extruder, a twin screw extruder, or a continuous kneader from the viewpoints of economy, processing efficiency, and the like. Further, two or more continuous melt-kneading apparatuses of the same type or different types may be used in combination.

  The L / D ratio (ratio between the screw effective length L and the outer diameter D) of the twin screw extruder is preferably 30 or more, and more preferably 36 to 60. In addition, as the twin screw extruder, for example, an arbitrary twin screw extruder such as one in which two screws mesh or not mesh can be used, but the rotation direction of the two screws is the same direction. Are more preferable. As such a twin screw extruder, for example, a trade name “PCM” (manufactured by Ikegai Co., Ltd.), a trade name “KTX” (manufactured by Kobe Steel), a trade name “TEX” (manufactured by Nippon Steel Works), a product The name “TEM” (manufactured by Toshiba Machine Co., Ltd.), the product name “ZSK” (manufactured by Warner), and the like can be mentioned.

  The L / D ratio (ratio between the screw effective length L and the outer diameter D) of the continuous kneader is preferably 5 or more, and more preferably 10 or more. Examples of such a continuous kneader include a trade name “Mixtron KTX / LCM / NCM” (manufactured by Kobe Steel), a trade name “CIM / CMP” (manufactured by Nippon Steel).

  The treatment temperature for the dynamic heat treatment is preferably 120 to 350 ° C, and more preferably 150 to 290 ° C. The treatment time is preferably 20 seconds to 320 minutes, more preferably 30 seconds to 25 minutes. Further, the shearing force to be applied is preferably 10 to 20000 / sec, more preferably 100 to 10,000 / sec in terms of shear rate.

2. Next, the molded member of the present invention will be described. One embodiment of the molded member of the present invention is formed by molding the thermoplastic elastomer composition for sealing materials described so far. Therefore, the molded member of the present embodiment is recyclable and has excellent strength, flexibility, solvent resistance, gas permeation resistance, and sealing properties, and is suitable as a sealing material and a tube material.

  The molded member of the present embodiment takes advantage of the characteristics as described above, and is used for capacitors, batteries, toner cases, inkjet printers including ink cartridges, FPDs (flat panel displays), household appliances, AV equipment, etc. It is suitable as various molded members (sealing material, tube material) for the housing. Moreover, if the sealing part is constituted by disposing the molding member of the present embodiment, a container having a sealing part having excellent sealing properties and the like can be provided.

  Note that the molded member of the present embodiment can be manufactured by various molding methods such as injection molding, press molding, and extrusion molding. In particular, it is preferable to manufacture by injection molding because it is possible to obtain a molded member having more excellent gas permeation resistance. This is presumed to be because the component (C) contained is oriented when the thermoplastic elastomer composition for sealing material of this embodiment is injection molded.

3. Next, the capacitor of the present invention will be described. FIG. 1 is a cross-sectional view schematically showing one embodiment of the capacitor of the present invention. A capacitor 5 shown in FIG. 1 includes a capacitor element 4, an outer case 3, and a sealing material 1. The capacitor element 4 is provided with a lead wire 2 for taking out electricity to the outside. The exterior case 3 has one or more openings 6 and can accommodate the capacitor element 4 therein. And the sealing material 1 is arrange | positioned so that the opening part 6 of the exterior case 3 which accommodated the capacitor | condenser element 4 in the inside may be sealed.

  The sealing material 1 of the capacitor 5 of the present embodiment is a sealing material made of the above-described thermoplastic elastomer composition for sealing material. For this reason, this sealing material 1 is recyclable and excellent in strength, flexibility, solvent resistance, gas permeation resistance, and sealing properties. Therefore, the capacitor 5 of this embodiment provided with this sealing material 1 is excellent in airtightness. Further, since the sealing property of the sealing material 1 is extremely excellent, the electrolytic solution or the like enclosed in the outer case 3 is hardly deteriorated or leaked. Therefore, the capacitor 5 of this embodiment has a characteristic that it can be used for a long time. Furthermore, even if the sealing material 1 is a case where the shape is made thin, sufficient sealing performance is exhibited. Therefore, the capacitor 5 of this embodiment using this sealing material 1 can be downsized in its overall structure.

  The capacitor 5 of this embodiment can be manufactured by the method shown below, for example. First, the capacitor element 4 is produced by winding the anode foil and the cathode foil connected with the lead wire 2 through a separator. The capacitor element 4 is impregnated with an electrolytic solution and then accommodated in an outer case 3 made of a metal material such as aluminum. Subsequently, the capacitor | condenser 5 can be manufactured by arrange | positioning the sealing material 1 to the opening part of the exterior case 3, and performing shape processing, such as restrict | squeezing the opening part 6 from the outside.

  EXAMPLES Hereinafter, although this invention is demonstrated concretely based on an Example, this invention is not limited to these Examples. In the examples and comparative examples, “parts” and “%” are based on mass unless otherwise specified. Moreover, the measuring method of various physical-property values and the evaluation method of various characteristics are shown below.

[Tensile test]: Based on JIS K6251, tensile strength T _B (MPa) and tensile elongation E _B (%) were measured.

  [Hardness]: Hardness (HS (Duro A)) was measured according to JIS K6253.

[Solvent Permeation Test]: The amount of permeation was calculated from the value measured by the cup method. Specifically, γ-butyrolactone is put in a cup having an inner diameter of 35 mm and a depth of 20 mm, and the cup is sealed with a sample molded into a sheet shape. The cup is left in an oven at 80 ° C., and the mass of the cup is measured every 24 hours. The mass of the cup before being put in the oven was defined as “initial mass”, and the transmittance ((mg · mm) / (m ² · h)) was calculated from the following formula (4).
Permeability = {[initial mass (mg) −mass after t days (mg)] × sample thickness (mm)} / {cup mouth area (m ² ) × test time (h)} (4)

  [Recycling characteristics]: Observe whether plastic deformation characteristics are observed at temperatures near the processing temperature (160 to 250 ° C.). If plastic deformation characteristics are observed, “○ (good recycling characteristics)” indicates that the plastic deformation characteristics are The case where it was not recognized was evaluated as "x (poor recycling characteristic)".

(Example 1)
Pressurized kneader (capacity 10 liters, manufactured by Moriyama Co., Ltd.) heated to 150 ° C., 75 parts of butyl rubber (trade name “Butyl268”, manufactured by JSR), and plate filler (magnesium silicate (talc), trade name “Mistron” "Vapor" (manufactured by Sierra Talc) was added and kneaded. Thereafter, 25 parts of polypropylene (trade name “PM900A”, manufactured by Sun Allomer Co., Ltd.) was further added. A kneaded material in a molten state was obtained by kneading at 40 rpm (shear rate 200 / sec) for 15 minutes until the polypropylene melted and each component was uniformly dispersed. The obtained kneaded material in a molten state was pelletized using a feeder ruder (manufactured by Moriyama Co., Ltd.) to obtain a kneaded material. 100 parts of the pelletized kneaded material and 2 parts of a cross-linking agent (trade name “Tacchi Roll 201”, manufactured by Taoka Chemical Co., Ltd.) pulverized into a powder form were put into a Henschel mixer and mixed for 30 seconds. Then, using a twin screw extruder (same direction complete meshing screw, L / D = 33.5, manufactured by Ikegai Co., Ltd.), 200 ° C., residence time 1 minute 30 seconds, 300 rpm (shear speed 400 / sec), And extruding while carrying out dynamic heat treatment to obtain a pellet-shaped thermoplastic elastomer composition (Example 1).

The obtained thermoplastic elastomer composition is injection-molded using an injection molding machine (model number “N-100”, manufactured by Nippon Steel Works Co., Ltd.) to evaluate the physical properties of a 120 mm × 120 mm × 2 mm sheet. A test piece was prepared. Tensile strength _{T B} of the fabricated test pieces 5 MPa, tensile elongation _{E B} is 410%, the hardness HS 76 points, the transmission amount is 230 as measured by solvent permeation test ^{(mg · mm) / (m} 2 · h), and The evaluation result of the recycling characteristics was “◯”.

(Examples 2 to 4, Comparative Example 1)
Except having set it as the mixing | blending prescription shown in Table 1, it carried out similarly to the case of the above-mentioned Example 1, and obtained the pellet-shaped thermoplastic elastomer composition (Examples 2-4, Comparative Example 1). The trade names and manufacturers of the various components and additives used are shown in Table 2. The obtained thermoplastic elastomer composition was injection-molded in the same manner as in Example 1 to prepare a test piece for evaluating physical properties. Table 1 shows the measurement results of various physical properties and the evaluation results of the properties of the prepared test pieces.

(Comparative Example 2)
Into a Banbury mixer heated to 100 ° C (capacity 1.7 liters, manufactured by Kobe Steel), various components / additives other than the crosslinking agent are added according to the formulation shown in Table 1 until each component is uniformly dispersed. The compounded rubber composition was obtained by kneading at 60 rpm for about 10 minutes. By adding 12 parts of a cross-linking agent (trade name “Tacchi Roll 201”, manufactured by Taoka Chemical Co., Ltd.) to a compounded rubber composition 308.5 parts using a 6 inch roll (manufactured by Kansai Roll Co., Ltd.) A compounded rubber composition containing a crosslinking agent (Comparative Example 2) was obtained. The trade names and manufacturers of the various components and additives used are shown in Table 2.

  The obtained rubber composition containing a crosslinking agent is press-molded at 200 ° C. for 45 minutes using a press machine (manufactured by Kansai Roll Co., Ltd.) and a mold mold, thereby obtaining a sheet-like physical property of 120 mm × 120 mm × 2 mm A test piece for evaluation was prepared. Table 1 shows the measurement results of various physical properties and the evaluation results of the properties of the prepared test pieces.

(Comparative Example 3)
Except for using the compounding formulation shown in Table 1, various components and additives other than the crosslinking agent and crosslinking aid were added and kneaded in the same manner as in Comparative Example 2 to obtain a compounded rubber composition. With respect to 186.2 parts of the obtained compounded rubber composition, 8.2 parts of a crosslinking agent (2) (trade name “Park Mill D-40”, manufactured by NOF Corporation) and a crosslinking aid (trade name “Valnoc DGM”) A rubber composition containing a crosslinking agent (Comparative Example 3) was obtained by adding 2.5 parts of Ouchi Shinsei Chemical Co., Ltd.) using a 6-inch roll (manufactured by Kansai Roll Co., Ltd.). The trade names and manufacturers of the various components and additives used are shown in Table 2. The obtained rubber composition containing a crosslinking agent was press-molded at 170 ° C. for 20 minutes in the same manner as in Comparative Example 2 to prepare a test piece for evaluating physical properties. Table 1 shows the measurement results of various physical properties and the evaluation results of the properties of the prepared test pieces.

  As shown in Table 1, when the thermoplastic elastomer compositions of Examples 1 to 4 are used, the solvent permeability is higher than when the thermoplastic elastomer compositions and rubber compositions of Comparative Examples 1 to 3 are used. It is clear that a recyclable sealing material that is low and excellent in tensile strength and tensile elongation (flexibility) can be produced.

  The thermoplastic elastomer composition for sealing materials of the present invention is recyclable and produces molded members such as sealing materials and tube materials that are excellent in strength, flexibility, solvent resistance, gas permeability resistance, and sealing properties. Is something that can be done. Therefore, the use of the sealing material comprising the thermoplastic elastomer composition for a sealing material of the present invention can provide a capacitor that is small in size and excellent in airtightness and can be used for a long time.

It is sectional drawing which shows typically one Embodiment of the capacitor | condenser of this invention.

Explanation of symbols

1 Sealing Material 2 Lead Wire 3 Exterior Case 4 Capacitor Element 5 Capacitor 6 Opening

Claims (10)

(A) at least one rubber component selected from the group consisting of ethylene / α-olefin copolymer rubber and isobutylene-isoprene copolymer rubber;
(B) at least one thermoplastic resin component selected from the group consisting of an α-olefin-based crystalline thermoplastic resin, an α-olefin-based amorphous thermoplastic resin, and a cyclic olefin-based thermoplastic resin;
(C) an inorganic compound,
A raw material composition in which the content ratio of the (A) rubber component is 10 to 90% by mass with respect to a total of 100% by mass of the (A) rubber component and the (B) thermoplastic resin component,
(D) A thermoplastic elastomer composition for a sealing material, which is dynamically heat-treated in the presence of a crosslinking agent and substantially does not contain a plasticizer and a softener.   The thermoplastic elastomer composition for sealing materials according to claim 1, wherein the inorganic compound (C) is at least one selected from the group consisting of montmorillonite, mica, talc, clay, kaolin, and graphite. For a total of 100 parts by mass of the (A) rubber component and the (B) thermoplastic resin component,
The thermoplastic elastomer composition for sealing materials according to claim 1 or 2, further comprising (E) 1 to 30 parts by mass of a hydrogenated diene polymer.   The thermoplastic elastomer composition for sealing materials according to any one of claims 1 to 3, wherein the (D) crosslinking agent is an organic peroxide and / or a phenolic crosslinking agent.   The molded member formed by shape | molding the thermoplastic elastomer composition for sealing materials as described in any one of Claims 1-4.   The molded member according to claim 5, wherein the thermoplastic elastomer composition for sealing material is injection molded.   The molded member according to claim 5 or 6, which is a sealing material or a tube material.   The molded member according to any one of claims 5 to 7, which is for a capacitor, a battery, a toner case, an inkjet printer including an ink cartridge, a flat panel display, or a housing. A container having a seal portion,
The container by which the said sealing part was comprised by arrange | positioning the sealing material which consists of a thermoplastic elastomer composition for sealing materials as described in any one of Claims 1-4.   The thermoplastic elastomer composition for a sealing material according to any one of claims 1 to 4, wherein the capacitor element, an exterior case containing at least one opening that accommodates the capacitor element, and the opening are sealed. Capacitor with sealing material consisting of

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