JP2008111022A - Thermoplastic elastomer and thermoplastic elastomer composition - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a thermoplastic elastomer having excellent oil-resistance and mechanical strength, especially compression set while keeping excellent recyclability and to provide a thermoplastic elastomer composition containing the elastomer. <P>SOLUTION: The thermoplastic elastomer is composed of an elastomeric polymer having an epoxide, a hydroxyl group and a nitrogen-containing heterocyclic group, wherein the nitrogen-containing heterocyclic group is bonded to the main chain of the elastomeric polymer through a nitrogen atom or an oxygen atom. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention relates to a thermoplastic elastomer and a thermoplastic elastomer composition, and more specifically, thermoplasticity having a property (hereinafter, sometimes simply referred to as “recyclability”) capable of repeatedly reproducing cross-linking and cross-linking by temperature change. The present invention relates to an elastomer and a thermoplastic elastomer composition containing the elastomer.

In recent years, reuse of used materials is desired from the standpoints of environmental protection and resource saving. Cross-linked rubber (vulcanized rubber) has a stable three-dimensional network structure in which a polymer substance and a cross-linking agent (vulcanizing agent) are covalently bonded, and exhibits very high strength. Reforming is difficult. On the other hand, a thermoplastic elastomer utilizes physical cross-linking and can be easily molded by heating and melting without requiring a complicated vulcanization / molding process including pre-molding.
A typical example of such a thermoplastic elastomer includes a resin component and a rubber component, and at room temperature, the microcrystalline resin component serves as a hard segment serving as a crosslinking point of a three-dimensional network structure, and the rubber component (soft segment) Thermoplastic elastomers that prevent plastic deformation of the resin and that are plastically deformed by softening or melting of the resin component by increasing the temperature are known. However, since such a thermoplastic elastomer contains a resin component, the rubber elasticity tends to be lowered. Therefore, a material that can impart thermoplasticity without containing a resin component is required.

  In response to such a problem, the present inventor has previously proposed that a hydrogen-bonding thermoplastic elastomer comprising an elastomeric polymer having a carbonyl-containing group and a heterocyclic amine-containing group in the side chain is changed by temperature change using hydrogen bonding. It has been found that crosslinking and dissociation can be repeated, and a hydrogen-bonding thermoplastic elastomer comprising an elastomeric polymer having (i) a carbonyl-containing group and (ii) a heterocyclic amine-containing group in the side chain. As a proposed method for producing the thermoplastic elastomer, an elastomeric polymer having a cyclic acid anhydride group in the side chain and a heterocyclic amine-containing compound are chemically bonded to the cyclic amine-containing compound. A method for producing a thermoplastic elastomer is proposed in which a thermoplastic elastomer is obtained by reacting under a bonding temperature (see, for example, Patent Document 1). ).

  The thermoplastic elastomer having such characteristics has high industrial utility value and environmental protection value, and further high tensile strength is obtained, and there is no change in physical properties even after repeated cross-linking and dissociation. It is expected as a material with excellent recyclability.

  However, although the thermoplastic elastomer described in Patent Document 1 has recyclability, it may have poor oil resistance, and may not be suitable for applications requiring oil resistance.

JP 2000-169527 A

  Therefore, the present invention aims to provide a thermoplastic elastomer that retains excellent recyclability, is excellent in oil resistance, and is excellent in mechanical strength, particularly compression set, and a thermoplastic elastomer composition containing the same. And

As a result of intensive studies to solve the above-mentioned problems, the present inventors have found that a thermoplastic elastomer that can be obtained by a predetermined reaction maintains excellent recyclability, excellent oil resistance, and mechanical strength, particularly compression permanent. The present inventors have found that the strain is excellent and have achieved the present invention.
That is, this invention provides the thermoplastic elastomer and thermoplastic elastomer composition as described in the following (i)-(viii).

(I) an elastomeric polymer having an epoxide, a hydroxyl group and a nitrogen-containing heterocycle;
A thermoplastic elastomer in which the nitrogen-containing heterocycle is bonded to the main chain of the elastomeric polymer through a nitrogen atom or an oxygen atom.

  (Ii) The thermoplastic elastomer according to the above (i), which has a structure represented by the following formula (1).

（式中、Ａは含窒素複素環である。）

(In the formula, A is a nitrogen-containing heterocyclic ring.)

  (Iii) The thermoplastic elastomer according to the above (i) or (ii), which has a structure represented by any of the following formulas (2a) to (2c).

（式中、Ａは含窒素複素環を表し、Ｒ¹〜Ｒ³はそれぞれ独立に水素原子、アルキル基、アリール基またはアルキル基にアリール基が置換したアラルキル基を表す。）

(In the formula, A represents a nitrogen-containing heterocyclic ring, and R ^{1 to} R ³ each independently represents a hydrogen atom, an alkyl group, an aryl group, or an aralkyl group in which an aryl group is substituted with an alkyl group.)

  The nitrogen-containing heterocycle is preferably a 5- or 6-membered ring.

  The nitrogen-containing heterocycle is preferably a triazole ring, thiazole ring, imidazole ring, pyridine ring, thiadiazole ring or hydantoin ring.

  (Iv) The heat according to any one of the above (i) to (iii) obtained by the reaction of the compound (A) having an epoxide and the compound (B) having an amino group or a hydroxyl group and a nitrogen-containing heterocyclic ring Plastic elastomer.

  (V) The thermoplastic elastomer according to (iv), wherein the compound (A) is an epoxidized elastomer.

  (Vi) The epoxidized elastomer is an epoxidized natural rubber, a styrene elastomer having an epoxide, an acrylic rubber having an epoxide, an ethylene-glycidyl methacrylate-methyl acrylate copolymer or an ethylene-glycidyl methacrylate-vinyl acetate copolymer. The thermoplastic elastomer according to (v) above.

  (Vii) The above (iv) to (vi) wherein the compound (B) is 3-amino-1,2,4-triazole, 2-aminothiazole, 4-aminopyridine or 2-butyl-4-hydroxymethylimidazole. The thermoplastic elastomer according to any one of the above.

  (Viii) A thermoplastic elastomer composition containing the thermoplastic elastomer according to any one of (i) to (vii) above.

  As described below, the present invention is useful because it can provide a thermoplastic elastomer that retains excellent recyclability, is excellent in oil resistance, and is excellent in mechanical strength, particularly compression set. is there. Moreover, the composition containing this thermoplastic elastomer also has the same effect and is very useful because its value is extremely high.

The present invention is described in detail below.
The thermoplastic elastomer according to the first aspect of the present invention (hereinafter sometimes simply referred to as “the thermoplastic elastomer of the present invention”) is composed of an elastomeric polymer having an epoxide, a hydroxyl group, and a nitrogen-containing heterocycle, A thermoplastic elastomer in which a nitrogen-containing heterocycle is bonded to the main chain of the elastomeric polymer through a nitrogen atom or an oxygen atom.

In the present invention, the epoxide refers to an oxide having a three-membered ring, and two carbon atoms forming the three-membered ring may constitute a part of the main chain of the elastomeric polymer. It may exist via a chemically stable bond (for example, a covalent bond, an ionic bond, etc.) with the main chain of the polymer.
In the present invention, the hydroxyl group does not include a hydroxyl group constituting a part of the carboxy group.

The reason why the thermoplastic elastomer of the present invention retains excellent recyclability, is excellent in oil resistance, and is excellent in mechanical strength, particularly compression set is not clear in detail. I think so.
Since the thermoplastic elastomer has a very large number of hydrogen-bonding cross-linked sites in its structure, that is, it has a hydroxyl group and a nitrogen-containing heterocycle, and the nitrogen-containing heterocycle is a nitrogen atom or Since it is bonded to the main chain via an oxygen atom, it is considered that excellent recyclability is maintained and that mechanical strength, particularly compression set, is excellent.
Similarly, it is considered that the thermoplastic elastomer is excellent in oil resistance because it has an epoxide in its structure.

The elastomeric polymer that is the main chain of the thermoplastic elastomer of the present invention is generally a known natural polymer or synthetic polymer, and a glass transition point of a polymer having a glass transition temperature of room temperature (25 ° C.) or lower, that is, an elastomer. If it does not specifically limit.
Specific examples of such elastomeric polymers include natural rubber (NR), isoprene rubber (IR), butadiene rubber (BR), 1,2-butadiene rubber, styrene-butadiene rubber (SBR), and acrylonitrile. -Diene rubbers such as butadiene rubber (NBR), chloroprene rubber (CR), butyl rubber (IIR), ethylene-propylene-diene rubber (EPDM), and hydrogenated products thereof; ethylene-propylene rubber, ethylene-acrylic rubber (AEM) Olefin-based rubbers such as ethylene-butene rubber (EBM), chlorosulfonated polyethylene, acrylic rubber, fluororubber, polyethylene rubber, and polypropylene rubber; epichlorohydrin rubber; polysulfide rubber; silicone rubber; urethane rubber;

  Further, the elastomeric polymer may be an elastomeric polymer containing a resin component, and specific examples thereof may be a hydrogenated polystyrene elastomeric polymer (for example, SBS, SIS, SEBS, etc.), Examples include polyolefin-based elastomeric polymers, polyvinyl chloride-based elastomeric polymers, polyurethane-based elastomeric polymers, polyester-based elastomeric polymers, and polyamide-based elastomeric polymers.

Further, the elastomeric polymer may be liquid or solid, and the molecular weight thereof is not particularly limited, and the thermoplastic elastomer of the present invention and the thermoplastic elastomer composition according to the second aspect of the present invention (hereinafter referred to as the following) It can be appropriately selected according to the use in which the “composition of the present invention” is used, the physical properties required for the composition of the present invention, and the like.
When the thermoplastic elastomer of the present invention and the composition of the present invention (hereinafter sometimes simply referred to as “the thermoplastic elastomer of the present invention (composition)”) are heated (decrosslinked) when the fluidity is emphasized The elastomeric polymer is preferably in a liquid state. For example, in diene rubbers such as isoprene rubber and butadiene rubber, the weight average molecular weight is preferably 1,000 to 100,000, and 1,000 to 50, It is especially preferable that it is about 000.
On the other hand, when emphasizing the strength of the thermoplastic elastomer (composition) of the present invention, the elastomeric polymer is preferably solid. For example, in diene rubbers such as isoprene rubber and butadiene rubber, the weight average molecular weight Is preferably 100,000 or more, particularly preferably about 500,000 to 1,500,000.
In the present invention, the weight average molecular weight is a weight average molecular weight (polystyrene conversion) measured by gel permeation chromatography (GPC). For the measurement, tetrahydrofuran (THF) is preferably used as a solvent.

In the present invention, two or more of the above elastomeric polymers can be mixed and used. In this case, the mixing ratio of the respective elastomeric polymers may be any ratio depending on the use of the thermoplastic elastomer (composition) of the present invention, the physical properties required for the thermoplastic elastomer (composition) of the present invention, and the like. It can be.
The glass transition point of the elastomeric polymer is preferably 25 ° C. or less as described above. When the elastomeric polymer has two or more glass transition points, or two or more elastomeric polymers are mixed. When used, at least one of the glass transition points is preferably 25 ° C. or lower. When the glass transition point of the elastomeric polymer is within this range, a molded product made of the thermoplastic elastomer (composition) of the present invention exhibits rubber-like elasticity at room temperature.
In the present invention, the glass transition point is a glass transition point measured by differential scanning calorimetry (DSC-Differential Scanning Calorimetry). The temperature raising rate is preferably 10 ° C./min.

  Such elastomeric polymers include natural rubber (NR), isoprene rubber (IR), butadiene rubber (BR), 1,2-butadiene rubber, styrene-butadiene rubber (SBR), ethylene-propylene-diene rubber (EPDM), Diene rubber such as butyl rubber (IIR); Olefin rubber such as ethylene-propylene rubber (EPM), ethylene-acrylic rubber (AEM), ethylene-butene rubber (EBM); Since the obtained molded product made of the thermoplastic elastomer (composition) of the present invention exhibits rubber-like elasticity at room temperature, it is preferable. Moreover, when an olefin rubber is used, deterioration of the composition is suppressed because there is no double bond.

In the present invention, the bound styrene amount of the styrene-butadiene rubber (SBR), the hydrogenation rate of the hydrogenated elastomeric polymer, and the like are not particularly limited, and the use of the thermoplastic elastomer (composition) of the present invention is not limited. The ratio can be adjusted to any ratio according to the physical properties required for the thermoplastic elastomer (composition) of the present invention.
When ethylene-propylene-diene rubber (EPDM), ethylene-acrylic rubber (AEM), ethylene-propylene rubber (EPM), ethylene-butene rubber (EBM) is used as the main chain of the elastomeric polymer, its ethylene content Is preferably 10 to 90 mol%, more preferably 40 to 90 mol%. It is preferable for the ethylene content to be in this range because the thermoplastic elastomer (composition) of the present invention is excellent in mechanical strength, particularly compression set.

  The thermoplastic elastomer of the present invention has an epoxide, a hydroxyl group and a nitrogen-containing heterocycle in the elastomeric polymer, and the nitrogen-containing heterocycle is bonded to the main chain of the elastomeric polymer via a nitrogen atom or an oxygen atom. It is a thermoplastic elastomer.

  In the present invention, the nitrogen-containing heterocycle of the elastomeric polymer is preferably bonded to the main chain of the elastomeric polymer via a nitrogen atom.

  Specifically, the thermoplastic elastomer of the present invention preferably has a structure represented by the following formula (1), and has a structure represented by any of the following formulas (2a) to (2c). More preferred.

In the above formula (1), A represents a nitrogen-containing heterocycle, and the bond on the side of the nitrogen atom that is not bonded to A does not represent a methyl group, but is bonded to the elastomeric polymer (for example, shared Bond, ionic bond, etc.).
In the above formulas (2a) to (2c), A represents a nitrogen-containing heterocyclic ring, and R ^{1 to} R ³ each independently represents a hydrogen atom, an alkyl group, an aryl group, or an aralkyl group in which an aryl group is substituted with an alkyl group. Represents.
Here, the free bond of each carbon atom in the formula (2a) does not represent a methyl group, and the bond between the two carbon atoms in the formula (2a) is the main chain of the elastomeric polymer. It constitutes a part of In addition, the free bond between the carbon atom to which R ² in the formula (2b) is bonded and the carbon atom to which R ¹ in the formula (2c) is bonded does not represent a methyl group, and the elastomeric polymer (For example, covalent bond, ionic bond, etc.).

Specific examples of the nitrogen-containing heterocycle as A in the above formula (1) include those shown below.
In addition, as the aralkyl group in which an aryl group is substituted for a hydrogen atom, an alkyl group, an aryl group, or an alkyl group, which is R ^{1 to} R ³ in the above formulas (2a) to (2c), specifically, for example, As the substituent X in the formulas (3) and (4) described later, an alkyl group having 1 to 30 carbon atoms, an aralkyl group having 7 to 20 carbon atoms, or an aryl group having 6 to 20 carbon atoms is preferably exemplified.

In the present invention, the nitrogen-containing heterocycle may have a heteroatom other than a nitrogen atom in the heterocycle, for example, a sulfur atom, an oxygen atom, a phosphorus atom, etc., as long as it contains a nitrogen atom in the heterocycle. Can be used.
The nitrogen-containing heterocycle may have a substituent, and specific examples of the substituent include alkyl groups such as a methyl group, an ethyl group, a (iso) propyl group, and a hexyl group; Alkoxy groups such as methoxy group, ethoxy group, (iso) propoxy group; groups consisting of halogen atoms such as fluorine atom, chlorine atom, bromine atom, iodine atom; cyano group; amino group; aromatic hydrocarbon group; ester group; An ether group; an acyl group; a thioether group; and the like can be mentioned, and these can be used in combination. The substitution position of these substituents is not particularly limited, and the number of substituents is not limited.

  Specific examples of such nitrogen-containing heterocycle include pyrrololine, pyrrolidone, oxindole (2-oxindole), indoxyl (3-oxindole), dioxindole, isatin, indolyl, phthalimidine, β -Isoindigo, monoporphyrin, diporphyrin, triporphyrin, azaporphyrin, phthalocyanine, hemoglobin, uroporphyrin, chlorophyll, phyroerythrin, imidazole, pyrazole, triazole, tetrazole, benzimidazole, benzopyrazole, benzotriazole, imidazoline, imidazolone, imidazolidone Hydantoin, pyrazoline, pyrazolone, pyrazolidone, indazole, pyridoindole, purine, cinnoline, pyrrole, pyrroline, in , Indoline, oxylindole, carbazole, phenothiazine, indolenine, isoindole, oxazole, thiazole, isoxazole, isothiazole, oxadiazole, thiadiazole, oxatriazole, thiatriazole, phenanthroline, oxazine, benzoxazine, phthalazine, pteridine , Pyrazine, phenazine, tetrazine, benzoxazole, benzoisoxazole, anthranyl, benzothiazole, benzofurazan, pyridine, quinoline, isoquinoline, acridine, phenanthridine, anthrazolin, naphthyridine, thiazine, pyridazine, pyrimidine, quinazoline, quinoxaline, triazine, histidine , Triazolidine, melamine, adenine, guanine, thymine, cytosine And derivatives thereof. Of these, the nitrogen-containing 5-membered ring is preferably exemplified by the following compounds, triazole derivatives represented by the following formula (3) and imidazole derivatives represented by the following formula (4). These may have the above-described various substituents, or may be hydrogenated or eliminated.

In the formula, the substituent X is an alkyl group having 1 to 30 carbon atoms, an aralkyl group having 7 to 20 carbon atoms, or an aryl group having 6 to 20 carbon atoms.
Specific examples of such substituent X include linear alkyl groups such as methyl group, ethyl group, propyl group, butyl group, pentyl group, octyl group, dodecyl group and stearyl group; isopropyl group Branched alkyl groups such as isobutyl group, s-butyl group, t-butyl group, isopentyl group, neopentyl group, t-pentyl group, 1-methylbutyl group, 1-methylheptyl group, 2-ethylhexyl group; benzyl group Aralkyl groups such as phenethyl group; aryl groups such as phenyl group, tolyl group (o-, m-, p-), dimethylphenyl group, mesityl group; and the like.
Among these, the alkyl group, in particular, the butyl group, the octyl group, the dodecyl group, the isopropyl group, and the 2-ethylhexyl group, have good fluidity at a high temperature of the thermoplastic elastomer (composition) of the present invention to be obtained. This is preferable.

  Moreover, about a nitrogen-containing 6-membered ring, the following compound is illustrated preferably. These may have various substituents as described above, or may be hydrogenated or eliminated.

  Moreover, what condensed the said nitrogen-containing heterocyclic ring, a benzene ring, or nitrogen-containing heterocyclic rings can also be used, Specifically, the following condensed ring is illustrated suitably. These condensed rings may also have the above-described various substituents, and may have hydrogen atoms added or eliminated.

Of such nitrogen-containing heterocycles, a 5-membered ring or a 6-membered ring is preferable. Specifically, a triazole ring, a thiazole ring, an imidazole ring, a pyridine ring, a thiadiazole ring, or a hydantoin ring can further improve the recyclability of the thermoplastic elastomer (composition) of the present invention and obtain mechanical strength. In particular, it is preferable because the compression set is further improved.
Further, among such nitrogen-containing heterocycles, having aromaticity, the resulting thermoplastic elastomer (composition) of the present invention has a higher tensile strength during crosslinking, mechanical strength, In particular, it is preferable because the compression set resistance becomes better.

  In the present invention, such a nitrogen-containing heterocycle is bonded to the main chain of the elastomeric polymer via a nitrogen atom or an oxygen atom, whereby the hydrogen bonding property of the thermoplastic elastomer of the present invention obtained is obtained. It is considered that the number of cross-linking sites increases, excellent recyclability is maintained, and mechanical strength, particularly compression set, is excellent.

Next, the bonding position of the nitrogen-containing heterocycle will be described. For convenience, the nitrogen-containing heterocycle is referred to as “nitrogen-containing n-membered ring compound (n ≧ 3)”.
The bonding positions described below ("positions 1 to n") are based on the IUPAC nomenclature. For example, in the case of a compound having three nitrogen atoms having an unshared electron pair, the bonding position is determined by the order based on the IUPAC nomenclature. Specifically, the bonding positions are indicated on the 5-membered, 6-membered and condensed nitrogen-containing heterocycles exemplified above.

  In the thermoplastic elastomer of the present invention, the bonding position of the nitrogen-containing n-membered ring compound bonded to the main chain of the elastomeric polymer through a nitrogen atom or an oxygen atom is not particularly limited, and any bonding position (position 1 to n) Rank). Preferably, it is the 1-position or 3-position to n-position.

When the nitrogen-containing n-membered ring compound has one nitrogen atom (for example, a pyridine ring), chelate is easily formed in the molecule and the physical properties such as tensile strength of the thermoplastic elastomer composition of the present invention are excellent. The 3rd to (n-1) positions are preferred.
By selecting the bonding position of the nitrogen-containing n-membered ring compound, the thermoplastic elastomer of the present invention is likely to form crosslinks due to hydrogen bonding, ionic bonding, coordination bonding, etc. between the thermoplastic elastomer molecules. The recyclability can be made better, and the mechanical strength, in particular, the compression set can be made better.

In the thermoplastic elastomer of the present invention, the epoxide is preferably contained in a proportion of 0.1 to 60% with respect to the monomer unit constituting the elastomeric polymer. When the ratio of having an epoxide is within this range, the oil resistance of the resulting thermoplastic elastomer (composition) of the present invention becomes better.
Similarly, the hydroxyl group is preferably contained in a proportion of 0.1 to 60% with respect to the monomer unit constituting the elastomeric polymer. When the proportion having a hydroxyl group is within this range, the recyclability and compression set of the thermoplastic elastomer (composition) of the present invention to be obtained become better.
Similarly, the nitrogen-containing heterocycle preferably has a ratio of 0.1 to 60% with respect to the monomer unit constituting the elastomeric polymer. When the ratio of the nitrogen-containing heterocyclic ring is within this range, the recyclability and compression set of the thermoplastic elastomer (composition) of the present invention to be obtained become better.

  The thermoplastic elastomer of the present invention is obtained by the reaction of a compound (A) having an epoxide and a compound (B) having an amino group or a hydroxyl group and a nitrogen-containing heterocyclic ring. This is preferable because an amino group (nitrogen atom) or an ether group (oxygen atom) having a high hydrogen bonding property for bonding to the main chain is easily generated.

<Compound having epoxide (A)>
As a compound (A) which has an epoxide, the epoxidized elastomer which has an epoxide in the said elastomeric polymer is mentioned, for example.
Specific examples of the epoxidized elastomer include epoxidized natural rubber, styrenic elastomer having epoxide, acrylic rubber having epoxide, ethylene-glycidyl methacrylate-methyl acrylate copolymer, ethylene-glycidyl methacrylate-vinyl acetate. A copolymer etc. are mentioned suitably.
Among these, epoxidized natural rubber and acrylic rubber having epoxide are preferable because the compression set of the resulting thermoplastic elastomer (composition) of the present invention becomes better.

In the present invention, as the epoxidized natural rubber, one obtained by epoxidizing natural rubber may be used, or a commercially available product may be used.
The method for epoxidizing natural rubber is not particularly limited, and examples thereof include a chlorohydrin method, a direct oxidation method, a hydrogen peroxide method, an alkyl hydroperoxide method, and a peracid method. Specifically, there is a method of reacting natural rubber with an organic peracid such as peracetic acid or performic acid.
Further, as commercially available products, specifically, for example, ENR-25 (epoxidation rate: 25%), ENR-50 (epoxidation rate: 50%), ENR-60 (manufactured by Malaysian Rubber Bureau (MRB)) Epoxidation rate: 60%) and the like.

  Moreover, in this invention, it is preferable that the epoxidation rate of an epoxidized natural rubber is 5-80 mol%, and it is more preferable that it is 5-60 mol%. If the epoxidation rate is within this range, the resulting thermoplastic elastomer of the present invention has better oil resistance.

On the other hand, as an acrylic rubber having an epoxide, specifically, for example, a monomer component that forms a main skeleton such as ethyl acrylate, butyl acrylate, or methoxyethyl acrylate, and a monomer that forms a crosslinking point such as glycidyl acrylate or glycidyl methacrylate. What is obtained by copolymerizing with a component may be used, and a commercial item may be used.
Specific examples of commercially available products include Nipol AR30 series, 40 series, and 50 series manufactured by Nippon Zeon Co., Ltd. Among them, AR54 is preferably used because of its low Tg and excellent cold resistance.

  In addition, the styrene elastomer having an epoxide is a styrene thermoplastic elastomer whose hard segment is polystyrene, and is an elastomer obtained by epoxidizing an unsaturated double bond portion contained in a conjugated diene component of a soft segment. In the invention, commercially available products such as Epofriend (for example, CT301, AT501) manufactured by Daicel Chemical Industries, Ltd. can be used.

  In addition, as the ethylene-glycidyl methacrylate-methyl acrylate copolymer, commercially available products such as Bond First 7L, 7M manufactured by Sumitomo Chemical Co., Ltd. can be used. Similarly, as the ethylene-glycidyl methacrylate-vinyl acetate copolymer, Commercially available products such as Bond First 2B and 7B manufactured by Sumitomo Chemical Co., Ltd. can be used.

<Compound (B) having amino group or hydroxyl group and nitrogen-containing heterocycle>
Specific examples of the compound (B) having an amino group or hydroxyl group and a nitrogen-containing heterocyclic ring include various examples having the amino group or hydroxyl group in the nitrogen-containing heterocyclic ring described above.
Among them, 3-amino-1,2,4-triazole, 3-amino-1,2,4-triazole-5-carboxylic acid, 4-amino-1,2,4-triazole, 1,2,4-triazole Triazole ring compounds such as -3-ol; 2-aminoimidazole, 2-butyl-4-hydroxymethylimidazole, 1- (2-hydroxyethyl) -2-methylimidazole, 4-hydroxymethyl-2-methylimidazole, etc. Preferable examples include imidazole ring compounds; thiazole ring compounds such as 2-aminothiazole; pyridine ring compounds such as 2-aminopyridine, 3-aminopyridine and 4-aminopyridine;

  The reaction conditions of the compound (A) and the compound (B) are not particularly limited because it is necessary to appropriately change mainly depending on the type of the compound (A), but epoxidized natural rubber is used as the compound (A). When used, the compound (A) and the compound (B) are preferably reacted under conditions of 100 ° C. or higher.

  The thermoplastic elastomer of the present invention preferably has a glass transition point of 25 ° C. or lower. When the thermoplastic elastomer has two or more glass transition points, or when two or more thermoplastic elastomers are used in combination, glass is used. At least one of the transition points is preferably 25 ° C. or lower. If the glass transition point is 25 ° C. or lower, the molded article exhibits rubber-like elasticity at room temperature.

Next, the composition of the present invention containing the thermoplastic elastomer of the present invention will be described.
The composition of the present invention contains one or more thermoplastic elastomers according to the first aspect of the present invention. The mixing ratio in the case of containing two or more kinds can be set to any ratio depending on the use of the composition, the physical properties required for the composition, and the like.

The composition of the present invention preferably contains carbon black and / or silica as a reinforcing agent.
The type of carbon black is appropriately selected according to the application. Generally, carbon black is classified into hard carbon and soft carbon based on the particle diameter. Soft carbon has low reinforcement to rubber, and hard carbon has strong reinforcement to rubber. In the present invention, it is particularly preferable to use hard carbon having strong reinforcing properties.
The content of carbon black (when used alone) is 0.1 to 200 parts by weight, preferably 1 to 100 parts by weight, based on 100 parts by weight of the thermoplastic elastomer of the present invention. More preferably, it is -80 mass parts.

Silica is not particularly limited, and specifically, for example, fumed silica, calcined silica, precipitated silica, pulverized silica, fused silica, diatomaceous earth, etc., the content (when silica alone is used) is The amount is from 0.1 to 200 parts by weight, preferably from 1 to 100 parts by weight, and more preferably from 1 to 80 parts by weight, based on 100 parts by weight of the thermoplastic elastomer of the present invention. Of these, precipitated silica is preferred.
When silica is used as the reinforcing agent, a silane coupling agent can be used in combination. Examples of the silane coupling agent include bis (triethoxysilylpropyl) tetrasulfide (Si69), bis (triethoxysilylpropyl) disulfide (Si75), γ-mercaptopropyltrimethoxysilane, vinyltrimethoxysilane, and the like. Moreover, the aminosilane compound mentioned later can also be used.

  When carbon black and silica are used in combination, the content (total amount of carbon black and silica) is 0.1 to 200 parts by mass and 1 to 100 parts by mass with respect to 100 parts by mass of the thermoplastic elastomer of the present invention. It is preferable that it is 1-80 mass parts.

  If necessary, the composition of the present invention introduces a polymer other than the thermoplastic elastomer of the present invention, a reinforcing agent (filler) other than carbon black and silica, and an amino group as long as the object of the present invention is not impaired. Fillers (hereinafter simply referred to as “amino group-introducing fillers”), amino group-containing compounds other than the amino group-introducing fillers, compounds containing metal elements (hereinafter simply referred to as “metal salts”), Maleic anhydride modified polymer, anti-aging agent, antioxidant, pigment (dye), plasticizer, thixotropic agent, UV absorber, flame retardant, solvent, surfactant (including leveling agent), dispersant, dehydration Various additives such as an agent, a rust preventive agent, an adhesion imparting agent, an antistatic agent, and a filler can be contained.

As the additive and the like, commonly used ones can be used, and specific examples thereof are shown below, but are not limited to those exemplified.
As the polymer other than the thermoplastic elastomer of the present invention, a polymer having a glass transition temperature of 25 ° C. or lower is preferable as described above. Specifically, for example, natural rubber (NR), isoprene rubber (IR), butadiene rubber (BR), 1,2-butadiene rubber, styrene-butadiene rubber (SBR), acrylonitrile-butadiene rubber (NBR), butyl rubber ( IIR), ethylene-propylene-diene rubber (EPDM), ethylene-propylene rubber (EPM), ethylene-acrylic rubber (AEM), ethylene-butene rubber (EBM), etc., and particularly the unsaturated bond of IIR, EPM, EBM. Polymers that do not have them or polymers with low unsaturated bonds (eg EPDM) are preferred. A polymer having a site capable of hydrogen bonding is also preferable, and examples thereof include polyester, polylactone, and polyamide. Further, thermoplastic polymers such as polyolefin-based soft resins, propylene-butene copolymers, ethylene-octene or ethylene-butene copolymers are also included.
In the composition of the present invention, the polymer other than the thermoplastic elastomer of the present invention may contain one kind or two or more kinds, and the content of the polymer is 100 parts by mass of the thermoplastic elastomer of the present invention. On the other hand, it is preferable that it is 0.1-200 mass parts, and it is more preferable that it is 1-100 mass parts.

  Specific examples of reinforcing agents other than carbon black and silica include, for example, iron oxide, zinc oxide, aluminum oxide, titanium oxide, barium oxide, magnesium oxide, calcium carbonate, magnesium carbonate, zinc carbonate, wax stone clay, and kaolin. Examples include clay and fired clay. The content of these reinforcing agents is preferably 0.1 to 200 parts by mass, and more preferably 1 to 100 parts by mass with respect to 100 parts by mass of the thermoplastic elastomer of the present invention.

  Examples of the filler that serves as a base for the amino group-introduced filler (hereinafter sometimes referred to simply as “filler that serves as a base”) include those exemplified as being able to be added to the crosslinked rubber as desired. From the viewpoint of ease of amino group introduction and easy adjustment of the introduction ratio (introduction ratio), silica, carbon black, and calcium carbonate are preferable, and silica is more preferable.

The amino group introduced into the filler serving as the substrate (hereinafter sometimes simply referred to as “amino group”) is not particularly limited, and specific examples thereof include aliphatic amino groups, aromatic amino groups, and complex groups. Examples thereof include an amino group constituting a ring and a plurality of mixed amino groups of these amino groups.
Here, in the present invention, an amino group having an amino group in an aliphatic amine compound is bonded to an aliphatic amino group, an aromatic group having an amino group bonded to an aromatic group, and an amino group having an amino group in a heterocyclic amine compound. It is called a heterocyclic amino group.
Among these, from the viewpoint of appropriately forming an interaction with the thermoplastic elastomer of the present invention and being effectively dispersible in the thermoplastic elastomer, a heterocyclic amino group and a mixed amino group containing a heterocyclic amino group are included. It is preferably a group or an aliphatic amino group, and preferably a heterocyclic amino group or an aliphatic amino group.

The series of the amino group is not particularly limited, and may be any of primary (—NH ₂ ), secondary (imino group,> NH), tertiary (> N—) or quaternary (> N ⁺ <). May be.
When the amino group is primary, the interaction with the thermoplastic elastomer of the present invention tends to be strong, and gelation may occur depending on the conditions for preparing the composition. On the other hand, when the amino group is tertiary, the interaction with the thermoplastic elastomer of the present invention tends to be weak, and there are cases where the effect of improving compression set or the like when the composition is obtained is small.
From such a viewpoint, the series of the amino group is preferably primary or secondary, and more preferably secondary.

  That is, the amino group is preferably a heterocyclic amino group, a mixed amino group containing a heterocyclic amino group, or a primary or secondary aliphatic amino group, and is preferably a heterocyclic amino group or a primary or secondary amino group. Particularly preferred is an aliphatic amino group.

  It is sufficient that at least one amino group is present on the surface of the filler serving as the substrate, but it is preferable to have a plurality of amino groups from the viewpoint of excellent effect of improving compression set when used as a composition.

In the case of having a plurality of amino groups, at least one of the plurality of amino groups is preferably a heterocyclic amino group, and further a primary or secondary amino group (an aliphatic amino group, an aromatic amino group, a complex amino group). It is more preferable to have a cyclic amino group.
Moreover, the kind and series of an amino group can arbitrarily adjust the said amino group according to the physical property requested | required of a composition.

The amino group-introduced filler is obtained by introducing the amino group into the filler serving as the substrate.
The method for introducing the amino group is not particularly limited, and specific examples thereof include surface treatment methods generally used for various fillers, reinforcing agents, etc. (for example, surface modification methods, surface coating methods, etc.). Can be mentioned. Preferred methods include a method of reacting a compound having a functional group capable of reacting with the filler serving as the substrate and an amino group with the filler (surface modification method), and a filler serving as the substrate with a polymer having an amino group. The method of coating the surface (surface coating method) or the method of reacting a compound having an amino group or the like in the synthesis process of the filler.

The amino group-introduced fillers may be used alone or in combination of two or more. The mixing ratio when two or more kinds are used in combination can be set to any ratio depending on the application in which the composition of the present invention is used, the physical properties required for the composition of the present invention, and the like.
The content of the amino group-introduced filler is preferably 0.1 to 200 parts by weight, more preferably 10 parts by weight or more, and 30 parts by weight with respect to 100 parts by weight of the thermoplastic elastomer of the present invention. Part or more is particularly preferable.

The amino group-containing compound other than the amino group-introduced filler will be described.
The amino group in the amino group-containing compound is basically the same as that described in the amino group-introduced filler, and is not particularly limited as long as the amino group content is 1 or more. It is preferable that the number is at least one because it can form two or more cross-linking bonds with the thermoplastic elastomer of the present invention and is excellent in the effect of improving physical properties.

The series of the amino group in the amino group-containing compound is not particularly limited, and is the same as the amino group in the amino group-introduced filler, primary (—NH ₂ ), secondary (imino group,> NH), tertiary ( > N-) or quaternary (> N ⁺ <), and may be used for physical properties such as recyclability, compression set, hardness and mechanical strength, particularly tensile strength, required for the composition of the present invention. It can be arbitrarily selected depending on the case. When a secondary amino group is selected, mechanical strength tends to be excellent, and when a tertiary amino group is selected, recyclability tends to be excellent. In particular, it is preferable to have two secondary amino groups because the resulting composition of the present invention is excellent in recyclability, compression set and mechanical strength, and in the balance of these physical properties.
In the case where the amino group-containing compound contains two or more amino groups, the number of primary amino groups in the amino group-containing compound is preferably 2 or less, and 1 or less. More preferably. When it has 3 or more primary amino groups, the (crosslinking) bond formed by the amino group and the functional group in the thermoplastic elastomer of the present invention (particularly, the carboxy group that is a carbonyl-containing group) is strengthened, and is excellent. Recyclability may be impaired.

  That is, considering the bonding strength between the functional group in the thermoplastic elastomer of the present invention and the amino group in the amino group-containing compound, the series and number of amino groups and the structure of the amino group-containing compound are appropriately adjusted and selected. be able to.

Specific examples of such an amino group-containing compound include N, N′-dimethylethylenediamine, N, N′-diethylethylenediamine, N, N′-diisopropylethylenediamine, N, N′-dimethyl-1,3- Propanediamine, N, N'-diethyl-1,3-propanediamine, N, N'-diisopropyl-1,3-propanediamine, N, N'-dimethyl-1,6-hexanediamine, N, N'- Secondary aliphatic diamines such as diethyl-1,6-hexanediamine and N, N ′, N ″ -trimethylbis (hexamethylene) triamine; Tertiary aliphatics such as tetramethyl-1,6-hexanediamine Diamines; polyamines containing aromatic primary amines such as aminotriazole and aminopyridine and heterocyclic amines; such as dodecylamine Alkyl monoamine; dipyridyl tertiary heterocyclic diamines and the like; and the like, compression set, mechanical strength, is preferably exemplified because improvement is high, especially tensile strength and the like.
Of these, secondary aliphatic diamines, polyamines containing aromatic primary amines and heterocyclic amines, or tertiary heterocyclic diamines are more preferred.

  In addition to these examples, a polymer compound having an amino group can be used as the amino group-containing compound.

The polymer compound having an amino group is not particularly limited, and specific examples thereof include polyamide, polyurethane, urea resin, melamine resin, polyvinylamine, polyallylamine, polyacrylamide, polymethacrylamide, polyaminostyrene, amino group-containing poly Examples thereof include polymers such as siloxane, and polymers obtained by modifying various polymers with a compound having an amino group.
The physical properties such as average molecular weight, molecular weight distribution, and viscosity of these polymers are not particularly limited, and may be any physical property depending on the application in which the composition of the present invention is used, the physical properties required for the composition of the present invention, and the like. be able to.

  The polymer compound having an amino group is preferably a polymer obtained by polymerizing (polyaddition or polycondensation) a condensable or polymerizable compound (monomer) having an amino group. A polysiloxane having an amino group which is a single condensate of a silyl compound having a group or a cocondensate of the silyl compound and a silyl compound having no amino group, is easily available, easy to produce, and has a molecular weight It is more preferable because it is easy to adjust the amino acid and the amino group introduction rate.

The silyl compound having a hydrolyzable substituent and an amino group is not particularly limited, and examples thereof include aminosilane compounds. Specifically, γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, γ An aminosilane compound having an aliphatic primary amino group such as aminopropylmethyldimethoxysilane, γ-aminopropylmethyldiethoxysilane, 4-amino-3,3-dimethylbutyltrimethoxysilane (manufactured by Nihon Unicar); N, N-bis [(3-trimethoxysilyl) propyl] amine, N, N-bis [(3-triethoxysilyl) propyl] amine, N, N-bis [(3-tripropoxysilyl) propyl] amine (Nippon Unicar Company), 3- (n-butylamino) propyltrimethoxysilane (Dyn Silane 1189 (manufactured by Degussa Huls)), N-ethyl-aminoisobutyltrimethoxysilane (Silquest A-Link 15 silane, manufactured by OSi Specialties) and other aminosilane compounds having an aliphatic secondary amino group; N-β (aminoethyl) ) Aliphatic primary such as γ-aminopropylmethyldimethoxysilane, N-β (aminoethyl) γ-aminopropyltrimethoxysilane, N-β (aminoethyl) γ-aminopropyltriethoxysilane (Nihon Unicar) And aminosilane compounds having secondary amino groups; aminosilane compounds having aromatic secondary amino groups such as N-phenyl-γ-aminopropyltrimethoxysilane (Nihon Unicar); imidazole trimethoxysilane (Japan Energy) Ami And the like are; triazole and epoxysilane compound or isocyanate silane compounds and the presence or absence of a catalyst, the aminosilane compound having a heterocyclic amino group, such as triazole silane obtained by reacting at room temperature or above.
Among these, from the viewpoint of high effect of improving physical properties such as compression set, the above-mentioned aminosilane compounds having an aliphatic primary amino group, aminosilane compounds having an aliphatic secondary amino group, and aliphatic primary and secondary It is preferably an aminoalkylsilane compound of an aminosilane compound having an amino group.

The silyl compound not having an amino group is not particularly limited as long as it is a compound different from the silyl compound having a hydrolyzable substituent and an amino group and does not contain an amino group. Examples include alkoxysilane compounds and halogenated silane compounds. Of these, alkoxysilane compounds are preferred from the viewpoints of availability, easy handling, and excellent physical properties of the resulting cocondensate.
Specific examples of the alkoxysilane compound include tetramethoxysilane, tetraethoxysilane, tetrabutoxysilane, tetraisopropoxysilane, methyltrimethoxysilane, methyltriethoxysilane, methyltributoxysilane, and methyltriisopropoxysilane. , Phenyltrimethoxysilane, dimethyldimethoxysilane and the like.
Specific examples of the halogenated silane compound include tetrachlorosilane and vinyltrifluorosilane.
Of these, tetraethoxysilane and tetramethoxysilane are preferred from the viewpoint of low cost and safe handling.

  The silyl compound having a hydrolyzable substituent and an amino group and the silyl compound not having an amino group may be used alone or in combination of two or more.

  Such a polymer compound having an amino group may be used alone or in combination of two or more. The mixing ratio when two or more kinds are used in combination can be set to any ratio depending on the application in which the composition of the present invention is used, the physical properties required for the composition of the present invention, and the like.

Further, the content of the polymer compound having an amino group can be defined by the number of nitrogen atoms (equivalent) in the compound with respect to the side chain of the thermoplastic elastomer of the present invention, as in the case of the amino group-containing compound. Depending on the structure and molecular weight of the polymer compound, there may be an amino group that cannot effectively form an interaction with the thermoplastic elastomer.
Therefore, the content of the polymer compound having an amino group is preferably 1 to 200 parts by mass, more preferably 5 parts by mass or more, with respect to 100 parts by mass of the thermoplastic elastomer of the present invention. It is particularly preferable that the amount is not less than part by mass.

The metal salt is not particularly limited as long as it is a compound containing at least one metal element, and is composed of Li, Na, K, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, and Al. A compound containing one or more metal elements selected from the group is preferable.
Specific examples of the metal salt include saturated fatty acid salts having 1 to 20 carbon atoms such as formate, acetate and stearate containing one or more of these metal elements, and (meth) acrylates. And unsaturated fatty acid salts such as, metal alkoxides (reactants with alcohols having 1 to 12 carbon atoms), nitrates, carbonates, bicarbonates, chlorides, oxides, hydroxides, complexes with diketones, and the like. .
Here, the “complex with diketone” refers to a complex in which a 1,3-diketone (for example, acetylacetone) or the like is coordinated to a metal atom.

  Among these, from the viewpoint of further improving the compression set of the composition of the present invention to be obtained, Ti, Al, Zn is preferable as the metal element, and carbon such as these acetates, stearates, etc. as the metal salts A complex with a saturated fatty acid salt having 1 to 20 carbon atoms, a metal alkoxide (reactant with an alcohol having 1 to 12 carbon atoms), an oxide, a hydroxide, or a diketone is preferable. Particularly preferred are saturated fatty acid salts, metal alkoxides (reactants with alcohols having 1 to 12 carbon atoms), and complexes with diketones.

  The said metal salt may be used individually by 1 type, or may use 2 or more types together. The mixing ratio when two or more kinds are used in combination can be set to any ratio depending on the application in which the composition of the present invention is used, the physical properties required for the composition of the present invention, and the like.

  The content of the metal salt is preferably 0.05 to 3.0 equivalents and more preferably 0.1 to 2.0 equivalents with respect to the carbonyl group contained in the thermoplastic elastomer of the present invention. Preferably, it is 0.2-1.0 equivalent. If the content of the metal salt is within this range, it is preferable because physical properties such as compression set, hardness and mechanical strength, particularly tensile strength, of the obtained composition of the present invention are improved.

In addition, as the metal salt, any hydroxide, metal alkoxide, carboxylate, or the like that the metal can take can be used. For example, taking a hydroxide as an example, when the metal is iron, Fe (OH) ₂ and Fe (OH) ₃ may be used alone or in combination.
Further, as described above, the metal salt is one or more selected from the group consisting of Li, Na, K, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, and Al. Although it is preferable that it is a compound containing a metal element, you may contain metal elements other than these in the range which does not impair the effect of this invention. Although the content rate of metal elements other than these is not specifically limited, For example, it is preferable that it is 1-50 mol% with respect to all the metal elements in the said metal salt.

  The maleic anhydride modified polymer is a polymer obtained by modifying the elastomeric polymer with maleic anhydride, and the side chain of the maleic anhydride modified polymer is other than the maleic anhydride residue and the nitrogen-containing heterocyclic ring. However, it is preferable to have only a maleic anhydride residue.

The maleic anhydride residue is introduced (modified) into the side chain or terminal of the elastomeric polymer and is not introduced into the main chain of the elastomeric polymer. The maleic anhydride residue is a cyclic acid anhydride group, and the cyclic acid anhydride group (part) does not open.
Therefore, as the maleic anhydride-modified thermoplastic polymer, for example, as shown in the following formula (5), a cyclic acid in the side chain obtained by reacting an ethylenically unsaturated bond portion of maleic anhydride with an elastomeric polymer is used. Examples include thermoplastic elastomers having an anhydride group and no nitrogen-containing heterocycle, and specific examples thereof include those exemplified for the above-described elastomeric polymer containing a cyclic acid anhydride group in the side chain. .

（式中、Ｑはエチレン残基またはプロピレン残基であり、ｐ、ｑおよびｒはそれぞれ独立に０．１〜９９の数を表す。）

(In the formula, Q is an ethylene residue or a propylene residue, and p, q and r each independently represents a number of 0.1 to 99.)

  The amount of maleic anhydride modification is preferably 0.1 to 50 mol% with respect to 100 mol% of the main chain portion of the elastomeric polymer from the viewpoint of improving compression set without impairing excellent recyclability. More preferably, it is 0.3-30 mol%, Most preferably, it is 0.5-10 mol%.

  The maleic anhydride-modified polymer may be used alone or in combination of two or more. The mixing ratio when two or more kinds are used in combination can be set to any ratio depending on the application in which the composition of the present invention is used, the physical properties required for the composition of the present invention, and the like.

The content of the maleic anhydride-modified polymer is preferably 1 to 100 parts by mass and more preferably 5 to 50 parts by mass with respect to 100 parts by mass of the thermoplastic elastomer of the present invention. If the content of the maleic anhydride-modified polymer is within this range, it is preferable because the processability and mechanical strength of the resulting composition of the present invention are improved.
In addition, when producing the thermoplastic elastomer of the present invention, specifically, in the reaction step A or B, if an elastomeric polymer containing a cyclic acid anhydride group in the side chain remains as an unreacted product, Without removing the carbonyl-containing group-modified elastomer, the composition of the present invention can be contained as it is.

Specific examples of the anti-aging agent include hindered phenol compounds, aliphatic and aromatic hindered amine compounds, and the like.
Specific examples of the antioxidant include butylhydroxytoluene (BHT) and butylhydroxyanisole (BHA).
Specific examples of the pigment include, for example, titanium dioxide, zinc oxide, ultramarine, bengara, lithopone, lead, cadmium, iron, cobalt, aluminum, hydrochloride, sulfate, and other inorganic pigments, azo pigments, copper phthalocyanine pigments, and the like. Organic pigments and the like.

Specific examples of the plasticizer include benzoic acid, phthalic acid, trimellitic acid, pyromellitic acid, adipic acid, sebacic acid, fumaric acid, maleic acid, itaconic acid, citric acid, and other polyesters. , Polyether, epoxy and the like.
Specific examples of the thixotropic agent include benton, silicic anhydride, silicic acid derivatives, urea derivatives, and the like.
Specific examples of the ultraviolet absorber include 2-hydroxybenzophenone, benzotriazole, and salicylic acid ester.
Specific examples of the flame retardant include phosphorus-based materials such as TCP, halogen-based materials such as chlorinated paraffin and perchlorpentacyclodecane, antimony-based materials such as antimony oxide, and aluminum hydroxide.

Specific examples of the solvent include hydrocarbons such as hexane and toluene; halogenated hydrocarbons such as tetrachloromethane; ketones such as acetone and methyl ethyl ketone; ethers such as diethyl ether and tetrahydrofuran; ethyl acetate. And ester systems such as
Specific examples of the surfactant (leveling agent) include polybutyl acrylate, polydimethylsiloxane, a modified silicone compound, and a fluorine-based surfactant.
Specific examples of the dehydrating agent include vinyl silane and the like.

Specific examples of the rust inhibitor include zinc phosphate, tannic acid derivatives, phosphate esters, basic sulfonates, and various rust preventive pigments.
Specific examples of the adhesion imparting agent include known silane coupling agents, silane compounds having an alkoxysilyl group, titanium coupling agents, zirconium coupling agents, and the like. More specifically, trimethoxyvinylsilane, vinyltriethoxysilane, vinyltris (2-methoxyethoxy) silane, γ-methacryloxypropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane and the like can be mentioned.
Generally as an antistatic agent, hydrophilic compounds, such as a quaternary ammonium salt or polyglycol and an ethylene oxide derivative, are mentioned.

  The content of the plasticizer is preferably 0.1 to 50 parts by mass, and more preferably 1 to 30 parts by mass with respect to 100 parts by mass of the thermoplastic elastomer of the present invention. The content of other additives is preferably 0.1 to 10 parts by mass and more preferably 1 to 5 parts by mass with respect to 100 parts by mass of the thermoplastic elastomer of the present invention.

Some of the thermoplastic elastomers of the present invention can self-crosslink, but vulcanizing agents, vulcanization aids, vulcanization accelerators, vulcanization retarders, etc. can be used in combination as long as the object of the present invention is not impaired. .
Examples of the vulcanizing agent include sulfur-based, organic peroxide-based, metal oxide-based, phenolic resin, quinone dioxime and other vulcanizing agents.
Specific examples of the sulfur vulcanizing agent include powdered sulfur, precipitated sulfur, highly dispersible sulfur, surface-treated sulfur, insoluble sulfur, dimorpholine disulfide, alkylphenol disulfide, and the like.
Specific examples of the organic peroxide vulcanizing agent include benzoyl peroxide, t-butyl hydroperoxide, 2,4-dichlorobenzoyl peroxide, 2,5-dimethyl-2,5-di- (T-Butylperoxy) hexane, 2,5-dimethylhexane-2,5-di (peroxylbenzoate) and the like.
Other examples include magnesium oxide, risurge (lead oxide), p-quinonedioxime, tetrachloro-p-benzoquinone, p-dibenzoylquinonedioxime, poly-p-dinitrosobenzene, and methylenedianiline.

Specific examples of the vulcanization aid include zinc oxide, magnesium oxide, and amines; fatty acids such as acetyl acid, propionic acid, butanoic acid, stearic acid, acrylic acid, and maleic acid; zinc acetylate, propionic acid. And fatty acid zinc such as zinc, zinc butanoate, zinc stearate, zinc acrylate, and maleate.
Specific examples of the vulcanization accelerator include thiurams such as tetramethylthiuram disulfide (TMTD) and tetraethylthiuram disulfide (TETD); aldehydes / ammonias such as hexamethylenetetramine; guanidines such as diphenylguanidine; Thiazoles such as 2-mercaptobenzothiazole and dibenzothiazyl disulfide (DM); sulfenes such as N-cyclohexyl-2-benzothiazylsulfenamide and Nt-butyl-2-benzothiazylsulfenamide Amide type; and the like. Furthermore, alkylphenol resins and their halides can also be used.
Specific examples of the vulcanization retarder include organic acids such as phthalic anhydride, benzoic acid, salicylic acid, and acetylsalicylic acid; N-nitrosodiphenylamine, N-nitrosophenyl-β-naphthylamine, N-nitroso- Nitroso compounds such as polymers of trimethyl-dihydroquinoline; halides such as trichloromelanin; 2-mercaptobenzimidazole; N- (cyclohexylthio) phthalimide (Santguard PVI);
The content of these vulcanizing agents is preferably 0.1 to 20 parts by mass and more preferably 1 to 10 parts by mass with respect to 100 parts by mass of the thermoplastic elastomer of the present invention.

  The method for producing the composition of the present invention is not particularly limited. For example, the thermoplastic elastomer of the present invention and various additives that may be contained as necessary are rolls, kneaders, pressure kneaders, Banbury mixers. And a method of producing by mixing using a single screw extruder, a twin screw extruder, a universal agitator, or the like.

  Curing conditions when the composition of the present invention is permanently cross-linked (by a vulcanizing agent) can be appropriately selected according to various components to be blended, and are not particularly limited. For example, curing conditions for curing at a temperature of 130 to 200 ° C. for 5 to 60 minutes are preferable.

When the thermoplastic elastomer (composition) of the present invention is heated to about 80 to 200 ° C., the three-dimensional crosslinked bond (crosslinked structure) is dissociated and softened to impart fluidity. This is considered to be because the interaction between the side chains formed between the molecules or within the molecule is weakened.
When the thermoplastic elastomer (composition) of the present invention that has been softened and given fluidity is allowed to stand at about 80 ° C. or less, the dissociated three-dimensional cross-linked bond (cross-linked structure) is re-bonded and cured. By repeating this, the thermoplastic elastomer (composition) of the present invention exhibits recyclability.

  The thermoplastic elastomer (composition) of the present invention can be used for various rubber applications utilizing, for example, rubber elasticity. Moreover, since it can improve heat resistance and recyclability, it is preferable to use it as a hot melt adhesive or as an additive contained therein. The thermoplastic elastomer (composition) of the present invention includes automobile surroundings, hoses, belts, sheets, anti-vibration rubber, rollers, linings, rubberized cloth, sealing materials, gloves, fenders, medical rubber (syringe gaskets, tubes) , Catheters), gaskets (for home appliances, construction), asphalt modifiers, hot melt adhesives, boots, grips, toys, shoes, sandals, keypads, gears, PET bottle cap liners, etc. Used.

  Specific examples of the above-mentioned automobile surroundings include, for example, tire treads, carcass, sidewalls, inner liners, under treads, belt portions, and the like; exterior radiator grilles, side moldings, garnishes (pillars, rears, cowls) Top), aero parts (air dam, spoiler), wheel cover, weather strip, cow belt grille, air outlet louver, air scoop, hood bulge, vent parts, anti-corrosion parts (over fender, side seal panel, molding ( Window, hood, door belt)), marks, etc .; interior window frame parts such as door, light, wiper weather strip, glass run, glass run channel; air duct hose, radiator hose, brake hose; crankshaft Lubricant, valve stem seal, head cover gasket, A / T oil cooler hose, mission oil seal, P / S hose, P / S oil seal and other lubricating oil parts; fuel hose, emission control hose, inlet filler hose, diaphragm Fuel system parts such as engine parts; Anti-vibration parts such as engine mounts and in-tank pump mounts; Boots such as CVJ boots and rack and pinion boots; Air conditioning parts such as A / C hoses and A / C seals; Belt parts such as timing belts and auxiliary belts; sealers such as windshield sealers, vinyl plastisol sealers, anaerobic sealers, body sealers, spot weld sealers; and the like.

  Further, when a rubber modifier, for example, a flow preventing agent, is included in a resin or rubber that causes a cold flow at room temperature, it is possible to prevent a flow during extrusion or a cold flow.

  The thermoplastic elastomer (composition) of the present invention is superior in oil resistance and mechanical strength while maintaining the same level of recyclability as compared to conventional thermoplastic elastomers. Among them, it is suitably used for applications requiring particularly recyclability, oil resistance and mechanical strength.

EXAMPLES Next, although an Example is shown and this invention is demonstrated more concretely, this invention is not limited to these.
(Examples 1-4 and Comparative Examples 1-3)
First, epoxidized natural rubber (ENR-50, epoxidation rate: 50%, manufactured by Malaysian Rubber Bureau (MRB)) and anti-aging agent (Irganox 1010, manufactured by Ciba Specialty Chemicals) ) Was added in the amount shown in Table 1 below and kneaded for 5 minutes.
Then, 3-amino-1,2,4-triazole (ATA, manufactured by Nippon Carbide), 2-aminothiazole (manufactured by Wako Pure Chemical Industries), 2-butyl-4-hydroxymethylimidazole (manufactured by Nippon Synthetic Chemical Co., Ltd.) ), 4-aminopyridine (manufactured by Koei Chemical Co., Ltd.), diethylenetriamine (manufactured by Tokyo Chemical Industry Co., Ltd.), 3-mercaptotriazole (manufactured by Otsuka Chemical Co., Ltd.) or 2-mercaptoimidazole (manufactured by Otsuka Chemical Co., Ltd.) The thermoplastic elastomer composition containing the thermoplastic elastomer was prepared by adding and kneading for 10 minutes to react. By performing IR analysis, it was confirmed that a thermoplastic elastomer having an epoxide, a hydroxyl group, and a nitrogen-containing heterocyclic ring was contained.

  About each thermoplastic elastomer composition obtained in Examples 1 to 4 and Comparative Examples 1 to 3, JIS-A hardness, tensile properties, compression set and oil resistance were measured by the method described later, and the recyclability was evaluated. . The results are shown in Table 1 below.

<JIS-A hardness>
Each obtained thermoplastic elastomer composition was hot-pressed at 180 ° C. for 10 minutes to produce a sheet having a thickness of 2 mm.
A disk-shaped test piece (diameter 29 mm) is punched from this sheet, and seven of the obtained disk-shaped test pieces are stacked and hot-pressed at 200 ° C. for 20 minutes, and the JIS-A hardness is measured according to JIS K6253. It was measured.

<Tensile properties>
Each obtained thermoplastic elastomer composition was hot-pressed at 180 ° C. for 10 minutes to produce a sheet having a thickness of 2 mm.
A No. 3 dumbbell-shaped test piece was punched out from this sheet, and a tensile test at a tensile speed of 500 mm / min was conducted in accordance with JIS K6251, and 100% modulus (M ₁₀₀ ) [MPa], 300% modulus (M ₃₀₀ ) [ MPa], breaking strength (T _B ) [MPa], and breaking elongation (E _B ) [%] were measured at room temperature.

<Compression set (C-Set)>
Each obtained thermoplastic elastomer composition was hot-pressed at 180 ° C. for 10 minutes to produce a sheet having a thickness of 2 mm.
Seven sheets prepared were stacked and hot-pressed at 200 ° C. for 20 minutes to prepare a cylindrical sample (diameter 29 × thickness 12.5 mm).
This cylindrical sample was compressed 25% with a dedicated jig and allowed to stand at 70 ° C. for 22 hours, and then the compression set was measured according to JIS K6262.

<Oil resistance>
Each obtained thermoplastic elastomer composition was hot-pressed at 180 ° C. for 10 minutes to produce a sheet having a thickness of 2 mm.
A disk-shaped test piece (diameter 29 mm) was punched from this sheet, immersed in JIS 3 oil at 23 ° C. for 168 hours, and the volume change rate (%) before and after immersion was measured.

<Recyclability>
Each obtained thermoplastic elastomer composition was hot-pressed at 200 ° C. for 10 minutes to produce a sheet having a thickness of 2 mm. This sheet was finely cut and press-molded again, and evaluated by the number of times that a seamless integrated sheet could be produced.
What was produced 10 times or more was set as "(circle)".

From the results shown in Table 1 above, the thermoplastic elastomer compositions prepared in Examples 1 to 4 were compared with the thermoplastic elastomer composition containing a thermoplastic elastomer having no nitrogen-containing heterocycle prepared in Comparative Example 1. The oil resistance was found to be excellent, and the mechanical strength, particularly compression set, was also excellent.
Further, the thermoplastic elastomer compositions prepared in Examples 1 to 4 are thermoplastics containing a thermoplastic elastomer in which the nitrogen-containing heterocycle prepared in Comparative Examples 1 and 2 is bonded to the main chain via a sulfur atom. Surprisingly, it was found that the oil resistance is remarkably excellent as compared with the elastomer composition, and the mechanical strength, particularly compression set, is remarkably excellent.

(Examples 5 and 6)
First, an acrylic rubber having an epoxide (AR54, manufactured by Nippon Zeon Co., Ltd.) and an anti-aging agent (Irganox 1010, manufactured by Ciba Specialty Chemicals Co., Ltd.) in a mass part shown in Table 2 below are charged into a pressure kneader set at 180 ° C. Kneaded for 5 minutes.
Thereafter, 3-amino-1,2,4-triazole (ATA, manufactured by Nippon Carbide Co., Ltd.) is added to the parts by mass shown in Table 2 below, and is further kneaded and reacted for 10 minutes to cause heat containing a thermoplastic elastomer. A plastic elastomer composition was prepared. By performing IR analysis, it was confirmed that a thermoplastic elastomer having an epoxide, a hydroxyl group, and a nitrogen-containing heterocyclic ring was contained.

About each thermoplastic elastomer composition obtained in Examples 5 and 6, JIS-A hardness, tensile properties, compression set and oil resistance were measured by the method described above, and the recyclability was evaluated. The results are shown in Table 2 below.
As for tensile properties, instead of measuring the 300% modulus (M ₃₀₀₎ [MPa], it was measured 50% modulus (M ₁₀₀₎ [MPa] and 200% modulus (M ₃₀₀₎ [MPa].
Moreover, about oil resistance, the volume change rate (%) at the time of being immersed in 70 degreeC JIS3 oil for 72 hours was further measured.

  From the results shown in Table 2 above, it was found that the thermoplastic elastomer compositions prepared in Examples 5 and 6 were also excellent in oil resistance and excellent in mechanical strength, particularly compression set.

Claims (8)

An elastomeric polymer having an epoxide, a hydroxyl group, and a nitrogen-containing heterocycle,
A thermoplastic elastomer in which the nitrogen-containing heterocycle is bonded to the main chain of the elastomeric polymer through a nitrogen atom or an oxygen atom. The thermoplastic elastomer according to claim 1, which has a structure represented by the following formula (1).

(In the formula, A represents a nitrogen-containing heterocyclic ring.) The thermoplastic elastomer of Claim 1 or 2 which has a structure represented by either of following formula (2a)-(2c).

(In the formula, A represents a nitrogen-containing heterocyclic ring, and R ^{1 to} R ³ each independently represents a hydrogen atom, an alkyl group, an aryl group, or an aralkyl group in which an aryl group is substituted with an alkyl group.)   The thermoplastic elastomer according to any one of claims 1 to 3, obtained by a reaction of a compound (A) having an epoxide and a compound (B) having an amino group or a hydroxyl group and a nitrogen-containing heterocyclic ring.   The thermoplastic elastomer according to claim 4, wherein the compound (A) is an epoxidized elastomer.   The epoxidized elastomer is an epoxidized natural rubber, a styrenic elastomer having an epoxide, an acrylic rubber having an epoxide, an ethylene-glycidyl methacrylate-methyl acrylate copolymer or an ethylene-glycidyl methacrylate-vinyl acetate copolymer. 5. The thermoplastic elastomer according to 5.   The compound (B) is 3-amino-1,2,4-triazole, 2-aminothiazole, 4-aminopyridine or 2-butyl-4-hydroxymethylimidazole. Thermoplastic elastomer.   A thermoplastic elastomer composition comprising the thermoplastic elastomer according to claim 1.