JP2005264067A - Thermoplastic elastomer composition - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a novel thermoplastic elastomer composition which has good physical properties, is excellent in rubbery elasticity, high-temperature creep performance, and moldability in an extensive temperature range and, though containing a thermoplastic elastomer, is excellent in oil resistance, heat resistance, and fuel oil resistance. <P>SOLUTION: The thermoplastic elastomer composition is one comprising (A) a (meth)acrylic block copolymer, (B) a compound having at least two amino groups in the molecule, (C) a thermoplastic resin, and (D) a plasticizer, wherein the (meth)acrylic block copolymer (A) is composed of (A1) (meth)acrylic polymer blocks and (A2) acrylic polymer blocks, where at least a polymer block of either type has at least one acid anhydride group in its main chain, and (meth)acrylic block copolymer (A) is dynamically crosslinked with compound (B) in the thermoplastic resin (C). <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

The present invention relates to a thermoplastic elastomer, has good physical properties, has a wide temperature range, is excellent in rubber elasticity, high temperature creep performance, molding processability, and is a thermoplastic elastomer, but also has oil resistance and heat resistance. The present invention relates to a novel thermoplastic elastomer composition excellent in fuel oil resistance.

Vulcanized rubber has excellent flexibility and rubber elasticity, but at the time of molding, it is necessary to add additives to the rubber and vulcanize, so the molding cycle time is long and the process is complicated, There is a problem in formability. Further, since the vulcanized rubber does not melt even after re-heating after being molded and vulcanized, there is a problem that post-processing such as joining cannot be performed and it is difficult to recycle after use. In view of the above, in recent years, thermoplastic elastomers have been used in place of vulcanized rubber.

Such thermoplastic elastomers include a type in which hard segments and soft segments are alternately contained in a copolymer chain (see, for example, Patent Document 1). These can be manufactured from those having high flexibility to those having rigidity by changing the proportion of each segment. Furthermore, a monoolefin copolymer rubber and a polyolefin resin are melt-kneaded using a crosslinking agent and a partially crosslinked composition, that is, a material having improved compression set by dynamic heat treatment (dynamic crosslinking). It is known (for example, see Patent Document 2).

However, in the case of a thermoplastic elastomer having a structure in which hard and soft segments are alternately contained in the former copolymer chain, a large amount of soft segments should be included in order to obtain a flexible thermoplastic elastomer. Is required. In addition, since the constraining component is a hard segment, it flows at a high temperature, but has a drawback of being inferior in heat resistance (heat resistance in this case means physical properties at high temperature) and compression set. In addition, since the soft segment has low tensile strength and heat resistance and oil resistance are poor, a flexible thermoplastic elastomer composition containing a large amount of such soft segments still has low tensile strength, heat resistance and oil resistance. Has the disadvantage of being bad and cannot be used for a wide range of applications. The technology disclosed as a conventional styrenic elastomer belongs to this category, and thus the moldability is very good. However, because of the above problems, it is used for a wide range of applications such as industrial mechanical parts. I can't. On the other hand, recently, acrylic block copolymers having a methacrylic copolymer block and an acrylic copolymer block have been disclosed as thermoplastic elastomers excellent in oil resistance. Is very good, but has disadvantages such as poor heat resistance and compression set (see, for example, Patent Document 3).

In the case of a thermoplastic elastomer with a structure in which the olefin copolymer rubber is partially crosslinked in the latter polyolefin, when the thermoplastic elastomer alone cannot provide sufficient performance, such as good compression set at high temperatures. Attempts have been made as a technique for improving performance.

However, crystalline polyolefins such as polyethylene and polypropylene have the disadvantage of being inferior in oil resistance due to their relatively low melting points, so that the composition obtained has only its parts that do not require oil resistance and heat resistance. Use has been limited. In recent years, as a solution to the above problems, by combining various thermoplastic resins such as polyester, polycarbonate, polyamide and various polar rubbers such as acrylic rubber, ethylene-acrylate copolymer rubber, nitrile rubber, Partially cross-linked thermoplastic elastomers have been studied (see, for example, Patent Documents 4, 5, and 6), but when a heat-resistant thermoplastic resin is used, the melting temperature is high, so that it is difficult to control cross-linking. The disadvantage that a good composition cannot be obtained and the conventional crosslinking agents for polar rubbers have the disadvantage that the properties of the resulting composition are lowered because the thermoplastic resin deteriorates during the curing process. Therefore, a thermoplastic elastomer material having oil resistance, heat resistance, good mechanical properties, and moldability is desired.
In addition, particularly in recent industrial applications, especially in automobile parts, development of recyclable thermoplastic elastomers that are not only excellent in heat resistance and oil resistance in the use environment but also excellent in fuel oil resistance is desired. So far, no material satisfying these characteristics has been obtained.
JP 61-34050 A Japanese Patent Publication No.53-21021 Japanese Patent No. 2553134 Japanese Patent Laid-Open No. 10-53697 JP-A-11-349734 JP 2000-26720 A

The present invention relates to a thermoplastic elastomer, has good physical properties, has a wide temperature range, is excellent in rubber elasticity, high temperature creep performance, molding processability, and is a thermoplastic elastomer, but also has oil resistance and heat resistance. The present invention relates to a novel thermoplastic elastomer composition excellent in fuel oil resistance.

The present inventors have (A) (meth) acrylic block copolymer comprising (A1) (meth) acrylic polymer block and (A2) acrylic polymer block, and (B) 2 in one molecule. A thermoplastic elastomer composition comprising a compound containing at least one amino group, (C) a thermoplastic resin, and (D) a plasticizer has an excellent balance between hardness and mechanical strength, rubber elasticity over a wide temperature range, and high temperature creep performance The present invention has been completed by finding that it is excellent in low temperature impact resistance, mechanical strength and molding processability, and is excellent in oil resistance, heat resistance and fuel oil resistance while being a thermoplastic elastomer.
That is, the present invention comprises (A) a (meth) acrylic block copolymer, (B) a compound containing two or more amino groups in one molecule, (C) a thermoplastic resin, and (D) a plasticizer. A thermoplastic elastomer composition comprising:
The (meth) acrylic block copolymer (A) is composed of (A1) (meth) acrylic polymer block and (A2) acrylic polymer block, and in the main chain of at least one polymer block, Formula (1):

(Wherein R ¹ is hydrogen or a methyl group, two R ^{1 s} may be the same or different from each other, n is an integer of 0 to 3, and m is an integer of 0 or 1). Having at least one
The present invention relates to a thermoplastic elastomer composition characterized in that a (meth) acrylic block copolymer (A) is dynamically crosslinked in a thermoplastic resin (C) with a compound (B).
In the present invention, the (meth) acrylic block copolymer (A) is a block copolymer represented by the general formula (A1-A2) _n , a block copolymer represented by the general formula A2- (A1-A2) _n. It is preferably at least one selected from the group consisting of a polymer and a block copolymer represented by formula (A1-A2) _n -A1 (n is an integer of 1 or more).
The (meth) acrylic block copolymer (A) comprises (meth) acrylic polymer block (A1) 0.1 to 60% by weight and acrylic polymer block (A2) 99.9 to 40% by weight. It is preferable.
The (meth) acrylic polymer block (A1) preferably has an acid anhydride group.
It is preferable that the acrylic polymer block (A2) has an acid anhydride group.
The (meth) acrylic block copolymer (A) is preferably obtained by controlled polymerization by atom transfer radical polymerization.
The thermoplastic resin (C) is preferably a polyamide-based resin and / or a polyester-based resin.
More preferably, the thermoplastic resin (C) is a polyamide-based resin.
The plasticizer (D) is preferably at least one selected from the group consisting of phthalic acid derivatives, hydroxybenzoic acid ester derivatives, benzenesulfonic acid alkylamide derivatives, and toluenesulfonic acid alkylamide derivatives.

The thermoplastic elastomer composition of the present invention has an excellent balance between hardness and mechanical strength, is excellent in rubber elasticity, high temperature creep performance and molding processability over a wide temperature range, and is a thermoplastic elastomer, but also has oil resistance and heat resistance. Since it is excellent in fuel oil resistance, it can be suitably used widely as various sealed containers, gaskets, oil resistant hoses, covering sheets and the like.

The present invention relates to a thermoplastic resin comprising a (meth) acrylic block copolymer (A), a compound (B) containing two or more amino groups in one molecule, a thermoplastic resin (C) and a plasticizer (D). An elastomer composition, wherein the (meth) acrylic block copolymer (A) comprises a (meth) acrylic polymer block (A1) and an acrylic polymer block (A2), and at least one polymer block In the main chain of general formula (1):

(Wherein R ¹ is hydrogen or a methyl group, two R ^{1 s} may be the same or different from each other, n is an integer of 0 to 3, and m is an integer of 0 or 1). Heat having at least one (a1), wherein the (meth) acrylic block copolymer (A) is dynamically cross-linked in the thermoplastic resin (C) by the compound (B) The present invention relates to a plastic elastomer composition.

Here, dynamically crosslinking means that (meth) acrylic block copolymer (A), compound (B) containing two or more amino groups in one molecule, and thermoplastic resin (C) are present. Crosslinking the (meth) acrylic block copolymer (A) and the compound (B) containing two or more amino groups in one molecule in the thermoplastic resin (C) by melt-kneading the system Thus, a thermoplastic elastomer composition having improved physical properties can be obtained. The morphology of this thermoplastic elastomer is that the crosslinked (meth) acrylic block copolymer (A) is dispersed in the thermoplastic resin (C) matrix that is a continuous phase in view of rubber elasticity and the like. It is preferable from the viewpoint of flexibility and the like that the crosslinked (meth) acrylic block copolymer (A) and the thermoplastic resin (C) have a co-continuous structure.

<(Meth) acrylic block copolymer (A)>
The structure of the (meth) acrylic block copolymer (A) used in the present invention is a linear block copolymer or a branched (star) block copolymer, and may be a mixture thereof. The structure of such a block copolymer is necessary for the required physical properties of the (meth) acrylic block copolymer (A), processing properties and mechanical properties required for the composition with the thermoplastic resin, etc. However, a linear block copolymer is preferable from the viewpoint of cost and ease of polymerization.

The (meth) acrylic block copolymer (A) comprises a (meth) acrylic polymer block (A1) and an acrylic polymer block (A2), and has physical properties of the composition such as tensile mechanical properties and compression set. In view of this, a block copolymer represented by the general formula (A1-A2) _n , a block copolymer represented by the general formula A2- (A1-A2) _n , and a general formula (A1-A2) _n- At least one selected from the group consisting of block copolymers represented by A1 (n is an integer of 1 or more) is preferred. Although not particularly limited, among these, from the viewpoint of easy handling during processing and physical properties of the composition, an A1-A2 type diblock copolymer, an A1-A2-A1 type or an A2-A1-A2 type tri A block copolymer or a mixture thereof is preferred.

In addition, since the (meth) acrylic block copolymer (A) is dynamically crosslinked by the compound (B) containing two or more amino groups in one molecule, the general formula (1):

(Wherein R ¹ is hydrogen or a methyl group, two R ^{1 s} may be the same or different from each other, n is an integer of 0 to 3, and m is an integer of 0 or 1). (A1).

The acid anhydride group (a1) represented by the general formula (1) can be one or more per polymer block, and when the number is two or more, the monomer is The mode being polymerized can be block copolymerization. For example, an x-y-x type triblock copolymer is represented by (x / z) -y-x type, (x / z) -y- (x / z) type, z-xy- x-type, z-x-y-x-z type, x- (y / z) -x-type, x-yz-x-type, x-z-y-x-type, x-z-yz Any of -x type etc. may be sufficient. Here, z represents a monomer or polymer block containing an acid anhydride group (a1), and (x / z) is a single monomer containing an acid anhydride group (a1) in the block body (x). The body is copolymerized, and (y / z) indicates that the block body (y) is copolymerized with a monomer containing an acid anhydride group (a1).

The number average molecular weight of the (meth) acrylic block copolymer (A) is not particularly limited, but is necessary for each of the (meth) acrylic polymer block (A1) and the acrylic polymer block (A2). It can be determined from the molecular weight. In the present invention, the number average molecular weight can be measured by gel permeation chromatography (GPC). The number average molecular weight can be directly measured for the (meth) acrylic block copolymer (A), but the acid anhydride group precursor is contained in terms of the reactivity of the acid anhydride group and the simplicity of the process. It is preferable to measure in the state of a (meth) acrylic block copolymer (A ′). If necessary, conversion based on the number average molecular weight obtained by measuring the content of acid anhydride groups and the precursor-containing (meth) acrylic block copolymer (A ′) of acid anhydride groups described below By doing, the number average molecular weight of a (meth) acrylic block copolymer (A) can also be calculated | required.

When the molecular weight of the (meth) acrylic block copolymer (A) is small, sufficient mechanical properties as an elastomer cannot be expressed, and conversely, when the molecular weight is larger than necessary, the processing properties deteriorate. The number average molecular weight of the acid anhydride group precursor-containing (meth) acrylic block copolymer (A ′) is preferably 3000 to 500000, more preferably 4000 to 400000, and still more preferably 5000 to 300000. .

Further, the ratio (Mw / Mn) of the weight average molecular weight (Mw) and the number average molecular weight (Mn) measured by gel permeation chromatography of the (meth) acrylic block copolymer (A) is not particularly limited. 1 to 1.8, more preferably 1 to 1.5. When Mw / Mn exceeds 1.8, the uniformity of the (meth) acrylic block copolymer may be lowered.

The composition ratio of the (meth) acrylic polymer block (A1) and the acrylic polymer block (A2) constituting the (meth) acrylic block copolymer (A) is not particularly limited, and is required for the use application. It may be determined from the physical properties required for processing the composition, the moldability required during processing of the composition, and the molecular weight required for each of the (meth) acrylic polymer block (A1) and the acrylic polymer block (A2). When the range of the composition ratio of the preferable (meth) acrylic polymer block (A1) and acrylic polymer block (A2) is exemplified, the (meth) acrylic polymer block (A1) is 0.1 to 80% by weight. The acrylic polymer block (A2) is preferably 99.9 to 20% by weight. More preferably, the (meth) acrylic polymer block (A1) is 0.1 to 70% by weight, and the acrylic polymer block (A2) is 99.9 to 30% by weight. More preferably, the (meth) acrylic polymer block (A1) is 0.1 to 60% by weight, and the acrylic polymer block (A2) is 99.9 to 40% by weight. When the proportion of the (meth) acrylic polymer block (A1) is less than 0.1% by weight, the rubber elasticity at high temperature may be lowered. Characteristics, particularly elongation at break, may decrease, and flexibility of the composition with the thermoplastic resin may decrease.

The relationship between the glass transition temperatures of the (meth) acrylic polymer block (A1) and the acrylic polymer block (A2) constituting the (meth) acrylic block copolymer (A) is as follows: (meth) acrylic polymer the glass transition temperature _{Tg A1} block (A1), its acrylic polymer block (A2) as _{Tg A2,} preferably satisfy the relation of the following equation.
Tg _A1 > Tg _A2

The glass transition temperature (Tg) of the polymer ((meth) acrylic polymer block (A1) and acrylic polymer block (A2)) is roughly set according to the following Fox formula, and each polymer portion This can be done by setting the weight ratio of the monomer.
_{1 / Tg = (W 1 /} Tg 1) + (W 2 / Tg 2) + ... + (W m / Tg m)
W ₁ + W ₂ + ... + W _m = 1

In the formula, Tg represents the glass transition temperature of the polymer, and Tg ₁ , Tg ₂ ,..., Tg _m represent the glass transition temperature of the polymer composed only of each monomer. W ₁ , W ₂ ,..., W _m represent the weight ratio of each monomer.

As the glass transition temperature of each monomer in the Fox formula, for example, a value described in Polymer Handbook Third Edition (Wiley-Interscience 1989) may be used.

General formula (1):

(Wherein R ¹ is hydrogen or a methyl group, two R ^{1 s} may be the same or different from each other, n is an integer of 0 to 3, and m is an integer of 0 or 1). The method for introducing (a1) into the (meth) acrylic block copolymer (A) is not particularly limited, but the acid anhydride group (a1) may be used in terms of ease of introduction and ease of purification after introduction. It is preferably introduced by introducing it into the (meth) acrylic block copolymer in the form of a functional group to be a precursor of, and then cyclizing.

N in General formula (1) is an integer of 0-3, Preferably it is 0 or 1, More preferably, it is 1. When n is 4 or more, polymerization tends to be complicated, and cyclization of the acid anhydride group tends to be difficult.

M in the general formula (1) is an integer of 0 or 1, and when n is 0, m is also preferably 0. When n is 1 to 3, m is preferably 1. .

The acid anhydride group (a1) may be contained in either one of the (meth) acrylic polymer block (A1) and the acrylic polymer block (A2) or in both blocks. You may do it. The reaction point of the (meth) acrylic block copolymer (A), the cohesive force and glass transition temperature of the block constituting the (meth) acrylic block copolymer (A), and further required (meth) Depending on the purpose, such as the physical properties of the acrylic block copolymer (A), the block into which the acid anhydride group should be introduced can be determined. For example, when controlling the molecular weight between cross-linking points, the acid anhydride group (a1) may be introduced into the (meth) acrylic polymer block (A1), and the compatibility with the thermoplastic resin (C) is controlled. In this case, the acid anhydride group (a1) may be introduced into the acrylic polymer block (A2). Although not particularly limited, in terms of reaction point control, heat resistance, rubber elasticity, etc., only one of the (meth) acrylic polymer block (A1) or the acrylic polymer block (A2) is used. It preferably has an acid anhydride group (a1). Although not particularly limited, but is preferably two R ¹ are both methyl (meth) may include an acid anhydride group (a1) acrylic polymer block (A1) has the general formula (1) , if containing an acid anhydride group (a1) in the acrylic polymer block (A2), 2 one of R ¹ in the general formula (1) is preferably both hydrogen. When (1) the acid anhydride group (a1) is contained in the (meth) acrylic polymer block (A1), R ¹ is hydrogen, or the acrylic polymer block (A2) contains the acid anhydride group (a1). In the case where R ¹ is a methyl group, the polymerization operation of the (meth) acrylic block copolymer (A) becomes complicated, or the (meth) acrylic polymer block (A1) and the acrylic polymer block The difference in the glass transition temperature of (A2) is reduced, and the rubber elasticity of the (meth) acrylic block copolymer (A) may be reduced.

The preferred range of the content of the acid anhydride group (a1) is the cohesive strength and reactivity of the acid anhydride group (a1), the structure and composition of the (meth) acrylic block copolymer (A), (meth) It varies depending on the number of blocks constituting the acrylic block copolymer (A), the glass transition temperature, and the site and manner in which the acid anhydride group (a1) is contained. If the preferable range of content of an acid anhydride group (a1) is illustrated, 0.05 to 50 weight% in the whole (meth) acrylic block copolymer (A) is preferable, and 0.1 to 40 weight% is preferable. More preferred. When the content of the acid anhydride group (a1) is less than 0.05% by weight, the reactivity of the (meth) acrylic block copolymer (A) and the compatibility with the thermoplastic resin are insufficient. When the amount exceeds 50% by weight, the rubber elasticity of the (meth) acrylic block copolymer (A) is reduced, or a large amount of crosslinking agent (B) is used to crosslink the (meth) acrylic block copolymer. ) May be necessary, or the fluidity of the resulting thermoplastic elastomer may be reduced by reaction with the thermoplastic resin (C). In addition, for the purpose of improving the heat resistance of the (meth) acrylic block copolymer (A), an acid anhydride group (a1) having a high Tg is introduced into the (meth) acrylic polymer block (A1) which is a hard segment. In such a case, if the content of the acid anhydride group (a1) is less than 0.05% by weight, the heat resistance may not be sufficiently improved, and the development of rubber elasticity at high temperatures may be reduced. Here, the content of the acid anhydride group (a1) is the total amount of the monomer unit originally having the acid anhydride group (a1) or the monomer unit represented by the general formula (1). Expressed in weight percent of the unit of the mass. This content can be calculated by ¹³ C-NMR analysis. Specifically, the resin is dissolved in heavy acetone, heavy chloroform, or the like, and ¹³ C-NMR analysis is performed. At this time, when the skeleton of the (meth) acrylic block copolymer is a (meth) acrylic acid ester, a signal of a carbonyl group derived from the (meth) acrylic acid ester unit is observed at 174 to 178 ppm, and 171 to 173 ppm. A signal derived from the carbonyl moiety of the (meth) acrylic anhydride skeleton is observed. By comparing these ratios, it is possible to quantify the acid anhydride group. When other copolymerizable monomers are introduced, monomer determination by GCMS using thermal decomposition and composition comparison by NMR or the like are performed.

The content block and content of the acid anhydride group (a1) may be appropriately determined according to the above, depending on the required reactivity, reaction point, cohesive force, glass transition temperature, and the like.

<(Meth) acrylic polymer block (A1)>
The monomer constituting the (meth) acrylic polymer block (A1) is (meth) from the viewpoint of easily obtaining a (meth) acrylic block copolymer having the desired physical properties, cost and availability. 100 to 50% by weight of an acrylic ester (including a monomer having an acid anhydride group (a1) when copolymerized with (A1)), and other vinyl monomers copolymerizable therewith It is preferably composed of 0 to 50% by weight of a monomer, and (meth) acrylic acid ester (including a monomer having an acid anhydride group (a1) when copolymerized with (A1)) is also included. More preferably, it consists of 0 to 25% by weight and other vinyl monomers copolymerizable therewith. When the proportion of (meth) acrylic acid ester (including a monomer having an acid anhydride group (a1) is present in (A1)) is less than 50% by weight, (meth) acrylic acid ester In some cases, the weather resistance, high glass transition point, compatibility with the resin, and the like, which are characteristics of the above, may be impaired.

The molecular weight required for the (meth) acrylic polymer block (A1) may be determined from the cohesive force required for the (meth) acrylic polymer block (A1) and the time required for the polymerization. .

The cohesive force is said to depend on the interaction between molecules and the degree of entanglement, and as the molecular weight increases, the entanglement point increases and the cohesive force increases. That is, the molecular weight required for the (meth) acrylic polymer block (A1) is M _A1, and the molecular weight between the entanglement points of the polymer constituting the (meth) acrylic polymer block (A1) is Mc _A1. Exemplifying the range of _A1 , when cohesive force is required, preferably M _A1 > Mc _A1 . As a further example, when further cohesive force is required, preferably M _A1 > 2 × Mc _A1 , and conversely, when it is desired to achieve both a certain cohesive force and creep property, Mc _A1 < M _A1 <2 × Mc _A1 is preferred. The molecular weight between the entanglement points may be referred to Wu et al. (Polymer Engineering and Science (Polym. Eng. And Sci., 1990, 30, p. 753), etc.) For example, a (meth) acrylic polymer block When the range of the number average molecular weight of the (meth) acrylic polymer block (A1) in the case where cohesive force is required assuming that (A1) is composed entirely of methyl methacrylate, it is 100 or more. In addition, since the polymerization time tends to be long when the number average molecular weight is large, it may be set according to the required productivity, but is preferably 200000 or less, more preferably 100000 or less.

Examples of the (meth) acrylic acid ester constituting the (meth) acrylic polymer block (A1) include methacrylic acid esters and acrylic acid esters.
Examples of the methacrylate ester include methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, n-pentyl methacrylate, and n-methacrylate. Methacrylic acid aliphatic carbonization such as hexyl, n-heptyl methacrylate, n-octyl methacrylate, 2-ethylhexyl methacrylate, nonyl methacrylate, decyl methacrylate, dodecyl methacrylate, stearyl methacrylate Hydrogen (for example, alkyl having 1 to 20 carbon atoms, preferably 1 to 10 carbons) ester; methacrylic acid alicyclic hydrocarbon ester such as cyclohexyl methacrylate and isobornyl methacrylate; aralkyl methacrylate such as benzyl methacrylate ester; Methacrylic acid aromatic hydrocarbon esters such as phenyl acrylate and toluyl methacrylate; methacrylic acid such as 2-methoxyethyl methacrylate and 3-methoxybutyl methacrylate and functional group-containing alcohols having etheric oxygen; Esters of: trifluoromethyl methacrylate, 2-trifluoroethyl methacrylate, 2-perfluoroethyl ethyl methacrylate, 2-perfluoroethyl-2-perfluorobutyl ethyl methacrylate, 2-methacrylic acid 2- Perfluoroethyl, perfluoromethyl methacrylate, diperfluoromethyl methyl methacrylate, 2-perfluoromethyl-2-perfluoroethyl methyl methacrylate, 2-perfluorohexyl ethyl methacrylate, methacrylic acid 2 - Fluoro decyl ethyl, etc. methacrylic acid fluorinated alkyl esters such as meta 2-perfluoro-hexadecyl acrylate and the like.

Examples of the acrylic ester constituting the (meth) acrylic polymer block (A1) include methyl acrylate, ethyl acrylate, n-propyl acrylate, n-butyl acrylate, isobutyl acrylate, and n-acrylate. Acrylic aliphatic hydrocarbons such as pentyl, n-hexyl acrylate, n-heptyl acrylate, n-octyl acrylate, 2-ethylhexyl acrylate, nonyl acrylate, decyl acrylate, dodecyl acrylate, stearyl acrylate ( For example, an alkyl ester having 1 to 20 carbon atoms, preferably 1 to 10 carbon atoms; acrylic acid alicyclic hydrocarbon ester such as cyclohexyl acrylate and isobornyl acrylate; aromatic aromatic hydrocarbon such as phenyl acrylate and toluyl acrylate Esters; acrylic acid Aralkyl esters of acrylic acid such as Nzyl; esters of acrylic acid such as 2-methoxyethyl acrylate and 3-methoxybutyl acrylate with functional group-containing alcohols having etheric oxygen; trifluoromethylmethyl acrylate, 2-acrylic acid 2- Trifluoromethylethyl, 2-perfluoroethylethyl acrylate, 2-perfluoroethyl-2-perfluorobutylethyl acrylate, 2-perfluoroethyl acrylate, perfluoromethyl acrylate, diperfluoromethylmethyl acrylate Acrylic acid such as 2-perfluoromethyl-2-perfluoroethylmethyl acrylate, 2-perfluorohexylethyl acrylate, 2-perfluorodecylethyl acrylate, 2-perfluorohexadecylethyl acrylate, etc. Etc. can be mentioned alkyl esters.

At least one of these is used. Among the above methacrylic acid esters or acrylic acid esters, in view of compatibility with the thermoplastic resin to be combined, cost and availability, methacrylic acid esters are preferred, methacrylic acid aliphatic hydrocarbon esters are more preferred, More preferred are alkyl methacrylates, and particularly preferred is methyl methacrylate.

Examples of vinyl monomers copolymerizable with the (meth) acrylic acid ester constituting the (meth) acrylic block copolymer (A) include carboxylic acid-containing unsaturated compounds, aromatic alkenyl compounds, and cyanide. Examples thereof include vinyl compounds, conjugated diene compounds, halogen-containing unsaturated compounds, silicon-containing unsaturated compounds, unsaturated dicarboxylic acid compounds, vinyl ester compounds, maleimide compounds, and the like.

Examples of the carboxylic acid-containing unsaturated compound include methacrylic acid and acrylic acid. Examples of the aromatic alkenyl compound include styrene, α-methylstyrene, p-methylstyrene, p-methoxystyrene, and the like. Examples of the vinyl cyanide compound include acrylonitrile and methacrylonitrile. Examples of the conjugated diene compound include butadiene and isoprene. Examples of the halogen-containing unsaturated compound include vinyl chloride, vinylidene chloride, perfluoroethylene, perfluoropropylene, and vinylidene fluoride. Examples of the silicon-containing unsaturated compound include vinyltrimethoxysilane and vinyltriethoxysilane. Examples of the unsaturated dicarboxylic acid compound include maleic anhydride, maleic acid, monoalkyl esters and dialkyl esters of maleic acid, fumaric acid, monoalkyl esters and dialkyl esters of fumaric acid, and the like. Examples of the vinyl ester compound include vinyl acetate, vinyl propionate, vinyl pivalate, vinyl benzoate, vinyl cinnamate, and the like. Examples of the maleimide compound include maleimide, methylmaleimide, ethylmaleimide, propylmaleimide, butylmaleimide, hexylmaleimide, octylmaleimide, dodecylmaleimide, stearylmaleimide, phenylmaleimide, cyclohexylmaleimide and the like. At least one of these is used.

These vinyl monomers can be selected preferably depending on the compatibility with the thermoplastic resin (C) and / or the plasticizer (D). In addition, methyl methacrylate polymer is almost quantitatively depolymerized by thermal decomposition, but in order to suppress it, acrylic acid esters such as methyl acrylate, ethyl acrylate, butyl acrylate, acrylic acid 2 -Methoxyethyl or a mixture thereof, or styrene can be copolymerized. Further, acrylonitrile can be copolymerized for the purpose of further improving oil resistance.

The glass transition temperature of the (meth) acrylic polymer block (A1) is preferably 0 ° C. or higher, more preferably room temperature or higher. The glass transition temperature (Tg) of the polymer ((meth) acrylic polymer block (A1)) is set by setting the weight ratio of the monomer in each polymer portion according to the Fox formula. Can be done. Here, the glass transition temperature is calculated according to the Fox equation using a value described in Polymer Handbook Third Edition (Wiley-Interscience 1989) as the glass transition temperature of each monomer.

<Acrylic polymer block (A2)>
The monomer constituting the acrylic polymer block (A2) has an acrylic ester (an acid anhydride group (a1) from the viewpoint of easily obtaining a composition having desired physical properties, cost and availability. The monomer preferably comprises 100 to 50% by weight (including this when copolymerized with (A2)), and 0 to 50% by weight of a vinyl monomer copolymerizable therewith. 100 to 75% by weight of an ester (including a monomer having an acid anhydride group (a1) when copolymerized with (A2)), and vinyl monomer 0 to copolymerize with ester More preferably, it consists of 25% by weight. When the proportion of the acrylic ester is less than 50% by weight, the physical properties of the composition, particularly the impact resistance, which is a characteristic when using the acrylic ester, may be impaired.

The molecular weight required for the acrylic polymer block (A2) may be determined from the elastic modulus and rubber elasticity required for the acrylic polymer block (A2), the time required for the polymerization, and the like.

The elastic modulus is closely related to the ease of movement of the molecular chain and its molecular weight, and the original elastic modulus is not shown unless the molecular weight exceeds a certain level. The same applies to rubber elasticity, but from the viewpoint of rubber elasticity, a higher molecular weight is desirable. That is, when the number average molecular weight required for the acrylic polymer block (A2) is exemplified as M _A2 , the range is preferably M _A2 > 3000, more preferably M _A2 > 5000, and more preferably M _A2 > 10000. Particularly preferably, M _A2 > 20000, and most preferably M _A2 > 40000. However, since the polymerization time tends to be longer when the number average molecular weight is large, the polymerization time may be set according to the required productivity, but is preferably 500,000 or less, more preferably 300,000 or less.

Examples of the acrylic ester constituting the acrylic polymer block (A2) include those described in the (meth) acrylic polymer block (A1), and the (meth) acrylic polymer block (A1). There is no particular limitation as long as it is not the same. At least one of these is used.

Among these, acrylic acid aliphatic hydrocarbon ester is preferable, and acrylic acid alkyl ester is more preferable. N-butyl acrylate is particularly preferred from the standpoint of impact resistance, cost, and availability of the thermoplastic elastomer composition. Further, when the composition needs oil resistance, ethyl acrylate is preferable. When low temperature characteristics are required, 2-ethylhexyl acrylate is preferable. Furthermore, when it is desired to achieve both oil resistance and low temperature characteristics, a mixture of ethyl acrylate, n-butyl acrylate, and 2-methoxyethyl acrylate is preferable.

Examples of the vinyl monomer copolymerizable with the acrylic ester constituting the acrylic polymer block (A2) include, for example, methacrylic ester, aromatic alkenyl compound, vinyl cyanide compound, conjugated diene compound, halogen Examples thereof include unsaturated compounds containing unsaturated compounds, unsaturated dicarboxylic acid compounds, vinyl ester compounds, maleimide compounds, and specific examples thereof include those described in the (meth) acrylic polymer block (A1). be able to. At least one of these is used.

These vinyl monomers have a glass transition temperature, an elastic modulus and a polarity required for the acrylic polymer block (A2), and physical properties required for the composition, thermoplastic resin (C) and / or plasticity. A preferable one can be selected depending on compatibility with the agent (D). For example, acrylonitrile can be copolymerized for the purpose of improving the oil resistance of the composition.

The glass transition temperature of the acrylic polymer block (A2) is preferably −100 ° C. or higher and 50 ° C. or lower, more preferably −100 ° C. or higher and 0 ° C. or lower. When the glass transition temperature is higher than 50 ° C., the rubber elasticity of the (meth) acrylic block copolymer (A) may be lowered. When the glass transition temperature is lower than −100 ° C., the (meth) acrylic block copolymer ( The mechanical strength of A) may decrease.

The glass transition temperature (Tg) of the polymer (acrylic polymer block (A2)) can be set by setting the monomer weight ratio of each polymer portion according to the Fox formula. it can. Here, the glass transition temperature is calculated according to the Fox equation using a value described in Polymer Handbook Third Edition (Wiley-Interscience 1989) as the glass transition temperature of each monomer.

<Acid anhydride group (a1)>
General formula (1):

(Wherein R ¹ is hydrogen or a methyl group, two R ^{1 s} may be the same or different from each other, n is an integer of 0 to 3, and m is an integer of 0 or 1). (A1) has high reactivity with a compound having an amino group, a hydroxyl group, etc., and therefore, as a reaction point in modifying the polymer, the reaction with the thermoplastic resin (C) and / or the plasticizer (D) It can also be used as a compatibility improvement site. Further, the acid anhydride group (a1) can become a crosslinking point by reaction with a compound (B) containing two or more amino groups in one molecule. Moreover, since it has high reactivity with a compound having an amino group, a hydroxyl group, etc., it can also be used as a compatibility improving site when blended with a thermoplastic resin. Furthermore, by introducing the acid anhydride group (a1) into a preferred site of the (meth) acrylic block copolymer (A), the desired site of the (meth) acrylic block copolymer (A) It is possible to crosslink. Moreover, since the acid anhydride group (a1) has a high glass transition temperature (Tg), when introduced into the hard segment, it has the effect of improving the heat resistance of the (meth) acrylic block copolymer (A). Have. The glass transition temperature of the polymer having an acid anhydride group (a1) is, for example, as high as 159 ° C. for polymethacrylic anhydride, and a (meth) acrylic block copolymer is introduced by introducing units constituting them. The heat resistance of (A) can be improved.

The method for introducing the acid anhydride group (a1) is not particularly limited, but the acid anhydride group (a1) is introduced into the (meth) acrylic block copolymer (A) in the form of a precursor, and thereafter It is preferable to cyclize. For example, the general formula (2):

(Wherein R ² represents hydrogen or a methyl group, R ³ represents hydrogen, a methyl group, or a phenyl group, and three R ³ represent at least two selected from a methyl group and / or a phenyl group) Except that they may be the same as or different from each other.) A precursor (meth) acrylic block copolymer (A ′) of an acid anhydride group characterized by having at least one monomer unit represented by ) Is preferably cyclized by heating at a temperature of 180 to 300 ° C. to introduce an acid anhydride group.

The introduction of the monomer unit represented by the general formula (2) is performed by introducing the monomer into the monomer constituting the (meth) acrylic polymer block (A1) and / or the acrylic polymer block (A2). It can carry out by copolymerizing with the monomer which comprises.
The monomer unit represented by the general formula (2) is eliminated and cyclized with an adjacent ester unit at a high temperature to generate an acid anhydride group (see, for example, Hatada et al., JMS -PURE APPL.CHEM., A30 (9 & 10), PP.645-667 (1993)). According to the above document, generally, in a polymer having a bulky ester unit and β-hydrogen, the ester unit is decomposed at a high temperature, followed by cyclization to produce an acid anhydride group. By utilizing the method described in the above document, an acid anhydride group can be easily introduced into the polymer into the (meth) acrylic block copolymer (A). Although not particularly limited, specifically, as such a monomer, t-butyl acrylate, isopropyl acrylate, α, α-dimethylbenzyl acrylate, α-methylbenzyl acrylate, t-butyl methacrylate, Examples include isopropyl methacrylate, α, α-dimethylbenzyl methacrylate, and α-methylbenzyl methacrylate. Of these, t-butyl acrylate and t-butyl methacrylate are preferable from the viewpoints of availability, ease of polymerization, and ease of acid anhydride group formation.

The formation of the acid anhydride group (a1) is preferably performed by heating the acid anhydride group precursor-containing (meth) acrylic block copolymer (A ′) at a high temperature, and is not particularly limited. It is preferable to heat at 180 to 300 ° C. When the temperature is lower than 180 ° C., the acid anhydride group may be insufficiently generated. When the temperature is higher than 300 ° C., the precursor (meth) acrylic block copolymer (A ′) itself of the acid anhydride group is decomposed. There is a case. In general, in the process of introducing an acid anhydride group, an ester unit decomposes at a high temperature to generate a carboxyl group, followed by cyclization and a part of the cyclization pathway in which an acid anhydride group is generated. When the acid anhydride group (a1) is introduced, a part of the carboxyl group may remain.

<Method for Producing Acid Anhydride Group Precursor (Meth) acrylic Block Copolymer (A ′)>
Although it does not specifically limit as a method of manufacturing the precursor containing (meth) acrylic block copolymer (A ') of the said acid anhydride group, It is preferable to use control polymerization. Examples of controlled polymerization include living anion polymerization, radical polymerization using a chain transfer agent, and recently developed living radical polymerization. Of these, living radical polymerization is preferable from the viewpoint of controlling the molecular weight and structure of the (meth) acrylic block copolymer.

Living radical polymerization is radical polymerization in which the activity at the polymerization terminal is maintained without loss. In the narrow sense, living polymerization refers to polymerization in which the terminal always has activity, but generally includes pseudo-living polymerization in which the terminal is inactivated and the terminal is in equilibrium. . The definition here is also the latter. Living radical polymerization has been actively researched by various groups in recent years.

Examples thereof include those using a chain transfer agent such as polysulfide, cobalt porphyrin complex (J. Am. Chem. Soc., 1994, 116, 7943) and nitroxide. Compounds using radical scavengers such as compounds (Macromolecules, 1994, 27, 7228), atom transfer radical polymerization using organic halides as initiators and transition metal complexes as catalysts (Atom Transfer) And Radical Polymerization (ATRP). In the present invention, there is no particular restriction as to which of these methods is used, but atom transfer radical polymerization is preferred from the viewpoint of ease of control.

In atom transfer radical polymerization, an organic halide or a sulfonyl halide compound is used as an initiator, and a metal complex having a group 8 element, group 9, group 10 or group 11 element as a central metal is used as a catalyst (for example, Matjajaszewski et al., Journal of American Chemical Society (J. Am. Chem. Soc.), 1995, 117, 5614; Macromolecules, 1995. 28, 7901; Science, 1996, 272, 866; or Sawamoto et al., Macromolecules, 1995, 28, 1721).

According to these methods, in general, the polymerization proceeds in a living manner and the molecular weight distribution is narrow (Mw / M), although the polymerization rate is very high and a radical reaction such as coupling between radicals is likely to occur. Mn = 1.1 to 1.5) polymer is obtained, and the molecular weight can be freely controlled by the charging ratio of the monomer and the initiator.

In the atom transfer radical polymerization method, as the organic halide or sulfonyl halide compound used as an initiator, a monofunctional, difunctional, or polyfunctional compound can be used. These may be properly used according to the purpose, but when producing a diblock copolymer, a monofunctional compound is preferable from the viewpoint of easy availability of an initiator, and a triblock of A1-A2-A1 type In the case of producing a copolymer, A2-A1-A2 type triblock copolymer, it is preferable to use a bifunctional compound from the viewpoint of the number of reaction steps and time reduction, and a branched block copolymer is used. In the case of production, it is preferable to use a polyfunctional compound in terms of the number of reaction steps and time reduction.

Moreover, it is also possible to use a polymer initiator as the initiator. The polymer initiator is a compound composed of a polymer in which a halogen atom is bonded to the end of a molecular chain among organic halides or sulfonyl halide compounds. Since such a polymer initiator can be produced by a controlled polymerization method other than the living radical polymerization method, a block copolymer obtained by combining polymers obtained by different polymerization methods is obtained. .

Examples of monofunctional compounds include:
C ₆ H ₅ -CH ₂ X,
_{C 6 H 5 -C (H)} (X) -CH 3,
_{C 6 H 5 -C (X)} (CH 3) 2,
R ⁴ —C (H) (X) —COOR ⁵ ,
R ⁴ —C (CH ₃ ) (X) —COOR ⁵ ,
R ⁴ —C (H) (X) —CO—R ⁵ ,
R ⁴ —C (CH ₃ ) (X) —CO—R ⁵ ,
R ⁴ —C ₆ H ₄ —SO ₂ X
And the like.

In the formula, C ₆ H ₅ represents a phenyl group, and C ₆ H ₄ represents a phenylene group (which may be ortho-substituted, meta-substituted, or para-substituted). R ⁴ represents a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, or an aralkyl group having 7 to 20 carbon atoms. X represents chlorine, bromine or iodine. R ⁵ represents a monovalent organic group having 1 to 20 carbon atoms.

Specific examples of the alkyl group having 1 to 20 carbon atoms (including the alicyclic hydrocarbon group) as R ⁴ include, for example, a methyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, an isobutyl group, Examples thereof include t-butyl group, n-pentyl group, n-hexyl group, cyclohexyl group, n-heptyl group, n-octyl group, 2-ethylhexyl group, nonyl group, decyl group, dodecyl group, isobornyl group and the like. Specific examples of the aryl group having 6 to 20 carbon atoms include a phenyl group, a tolyl group, a naphthyl group, and the like. Specific examples of the aralkyl group having 7 to 20 carbon atoms include benzyl group and phenethyl group.

Specific examples of the monofunctional compound include, for example, tosyl bromide, methyl 2-bromopropionate, ethyl 2-bromide propionate, butyl 2-bromide propionate, methyl 2-isobutyrate bromide, 2- Examples thereof include ethyl bromide isobutyrate and 2-butyl isobutyrate bromide. Of these, ethyl 2-bromide propionate and butyl 2-bromide propionate are preferred because they are similar to the structure of the (meth) acrylic acid ester monomer, and are easy to control polymerization.

As a bifunctional compound, for example,
_{X-CH 2 -C 6 H 4} -CH 2 -X,
_{X-CH (CH 3) -C} 6 H 4 -CH (CH 3) -X,
_{X-C (CH 3) 2} -C 6 H 4 -C (CH 3) 2 -X,
^{_{X-CH (COOR 6) -}} (CH 2) n -CH (COOR 6) -X,
^{_{X-C (CH 3) (}} COOR 6) - (CH 2) n -C (CH 3) (COOR 6) -X
^{_{X-CH (COR 6) -}} (CH 2) n -CH (COR 6) -X,
^{_{X-C (CH 3) (}} COR 6) - (CH 2) n -C (CH 3) (COR 6) -X,
_{X-CH 2 -CO-CH 2} -X,
X—CH (CH ₃ ) —CO—CH (CH ₃ ) —X,
_{X-C (CH 3) 2} -CO-C (CH 3) 2 -X,
_{X-CH (C 6 H 5} ) -CO-CH (C 6 H 5) -X,
X—CH ₂ —COO— (CH ₂ ) _n —OCO—CH ₂ —X,
_{X-CH (CH 3) -COO-} (CH 2) n -OCO-CH (CH 3) -X,
_{X-C (CH 3) 2} -COO- (CH 2) n -OCO-C (CH 3) 2 -X,
_{X-CH 2 -CO-CO-} CH 2 -X,
_{X-CH (CH 3) -CO} -CO-CH (CH 3) -X,
_{X-C (CH 3) 2} -CO-CO-C (CH 3) 2 -X,
_{X-CH 2 -COO-C 6} H 4 -OCO-CH 2 -X,
_{X-CH (CH 3) -COO} -C 6 H 4 -OCO-CH (CH 3) -X,
_{X-C (CH 3) 2} -COO-C 6 H 4 -OCO-C (CH 3) 2 -X,
_{X-SO 2 -C 6 H 4} -SO 2 -X
And the like.
In the formula, R ⁶ represents an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, or an aralkyl group having 7 to 20 carbon atoms. n represents an integer of 0 to 20. C ₆ H ₅ , C ₆ H ₄ and X are the same as described above.

Alkyl group having 1 to 20 carbon atoms R ^6, an aryl group having 6 to 20 carbon atoms, and specific examples of the aralkyl group having 7 to 20 carbon atoms, an alkyl group having 1 to 20 carbon atoms ^{R 4,} carbon atoms 6 The same thing as the specific example of a -20 aryl group and a C7-20 aralkyl group is mentioned.

Specific examples of the bifunctional compound include, for example, bis (bromomethyl) benzene, bis (1-bromoethyl) benzene, bis (1-bromoisopropyl) benzene, dimethyl 2,3-dibromosuccinate, and 2,3-dibromosuccinate. Diethyl acetate, dibutyl 2,3-dibromosuccinate, dimethyl 2,4-dibromoglutarate, diethyl 2,4-dibromoglutarate, dibutyl 2,4-dibromoglutarate, dimethyl 2,5-dibromoadipate, 2, Diethyl 5-dibromoadipate, dibutyl 2,5-dibromoadipate, dimethyl 2,6-dibromopimelate, diethyl 2,6-dibromopimelate, dibutyl 2,6-dibromopimelate, dimethyl 2,7-dibromosuberate, 2, , 7-dibromosuberic acid diethyl, 2,7-dibromosuberic acid Such as dibutyl, and the like. Of these, bis (bromomethyl) benzene, diethyl 2,5-dibromoadipate, and diethyl 2,6-dibromopimelate are preferred from the viewpoint of availability of raw materials.

As the multifunctional compound, for example,
_{C 6 H 3 - (CH 2} -X) 3,
_{C 6 H 3 - (CH (} CH 3) -X) 3,
_{C 6 H 3 - (C (} CH 3) 2 -X) 3,
_{C 6 H 3 - (OCO-} CH 2 -X) 3,
_{C 6 H 3 - (OCO-} CH (CH 3) -X) 3,
_{C 6 H 3 - (OCO-} C (CH 3) 2 -X) 3,
_{C 6 H 3 - (SO 2} -X) 3
And the like.
In the formula, C ₆ H ₃ is a trivalent phenyl group (the position of the three bonds may be any one of positions 1 to 6), and X is the same as described above.

Specific examples of the polyfunctional compound include, for example, tris (bromomethyl) benzene, tris (1-bromoethyl) benzene, tris (1-bromoisopropyl) benzene and the like. Of these, tris (bromomethyl) benzene is preferable from the viewpoint of availability of raw materials.

In addition, when an organic halide or sulfonyl halide compound having a functional group is used in addition to the group for initiating polymerization, a polymer in which a functional group other than the group for initiating polymerization is easily introduced at the terminal or in the molecule is obtained. It is done. Examples of functional groups other than the group that initiates polymerization include alkenyl groups, hydroxyl groups, epoxy groups, amino groups, amide groups, silyl groups, and the like.

The organic halide that can be used as the initiator is polymerized by activating the carbon-halogen bond, in which the carbon to which the halogen group (halogen atom) is bonded is bonded to the carbonyl group or the phenyl group. Is something that starts.
The amount of the initiator to be used may be determined from the molar ratio with the monomer in accordance with the required molecular weight of the (meth) acrylic block copolymer. That is, the molecular weight of the (meth) acrylic block copolymer can be controlled by the number of initiators used per molecule of monomer.

The transition metal complex used as the catalyst for the atom transfer radical polymerization is not particularly limited, but preferred are monovalent and zerovalent copper, divalent ruthenium, divalent iron, and divalent nickel. The complex of

Among these, a monovalent copper complex is preferable from the viewpoint of cost and reaction control. Examples of the monovalent copper compound include cuprous chloride, cuprous bromide, cuprous iodide, cuprous cyanide, cuprous oxide, cuprous perchlorate, and the like. Among these, cuprous chloride and cuprous bromide are more preferable from the viewpoint of polymerization control. When a monovalent copper compound is used, 2,2′-bipyridyl or a derivative thereof (for example, 4,4′-dinolyl-2,2′-bipyridyl, 4,4′-di (5- Noryl) -2,2'-bipyridyl and the like; 1,10-phenanthroline, derivatives thereof (for example, 4,7-dinolyl-1,10-phenanthroline, 5,6-dinolyl- 1,10-phenanthroline-based compounds such as 1,10-phenanthroline); polyamines such as tetramethyldiethylenetriamine (TMEDA), pentamethyldiethylenetriamine, and hexamethyl (2-aminoethyl) amine may be added as a ligand. .

A tristriphenylphosphine complex of divalent ruthenium chloride (RuCl ₂ (PPh ₃ ) ₃ ) is also preferable as a catalyst. When a ruthenium compound is used as a catalyst, aluminum alkoxides may be added as an activator. Furthermore, a divalent iron bistriphenylphosphine complex (FeCl ₂ (PPh ₃ ) ₂ ), a divalent nickel bistriphenylphosphine complex (NiCl ₂ (PPh ₃ ) ₂ ), and a divalent nickel bistributylphosphine A complex (NiBr ₂ (PBu ₃ ) ₂ ) is also preferable as a catalyst.

The catalyst, ligand and activator to be used are not particularly limited, but may be appropriately determined from the relationship between the initiator, monomer and solvent to be used and the required reaction rate. For example, in the polymerization of acrylic monomers such as acrylic acid esters, it is preferable from the viewpoint of polymerization control that the growth terminal of the polymer chain has a carbon-bromine bond, so that the initiator used is an organic bromide or It is a sulfonyl bromide compound, and the solvent is preferably acetonitrile, and a ligand such as pentamethyldiethylenetriamine is used using a metal complex catalyst having copper bromide, preferably copper contained in cuprous bromide as a central metal. Is preferably used. For polymerization of methacrylic monomers such as methacrylic acid esters, it is preferable from the viewpoint of polymerization control that the growth end of the polymer chain has a carbon-chlorine bond. It is a chloride or sulfonyl chloride compound, and the solvent is preferably a mixed solvent with acetonitrile, and if necessary toluene, etc., and a metal complex catalyst having copper as a central metal, preferably copper contained in cuprous chloride It is preferable to use a ligand such as pentamethyldiethylenetriamine.

The amount of catalyst and ligand to be used may be determined from the relationship between the amount of initiator, monomer and solvent to be used and the required reaction rate. For example, when trying to obtain a polymer with a high molecular weight, the initiator / monomer ratio must be smaller than when trying to obtain a polymer with a low molecular weight. Further, the reaction rate can be increased by increasing the number of catalysts and ligands. In addition, when a polymer having a glass transition point higher than room temperature is produced, the reaction rate tends to decrease when an appropriate organic solvent is added to lower the viscosity of the system and increase the stirring efficiency. In such a case, the reaction rate can be increased by increasing the number of catalysts and ligands.

The atom transfer radical polymerization can be carried out in the absence of a solvent (bulk polymerization) or in various solvents. Further, in bulk polymerization and polymerization performed in various solvents, the polymerization can be stopped halfway. Examples of the solvent include hydrocarbon solvents, ether solvents, halogenated hydrocarbon solvents, ketone solvents, alcohol solvents, nitrile solvents, ester solvents, carbonate solvents, and the like.

Examples of the hydrocarbon solvent include benzene and toluene. Examples of ether solvents include diethyl ether and tetrahydrofuran. Examples of the halogenated hydrocarbon solvent include methylene chloride and chloroform. Examples of the ketone solvent include acetone, methyl ethyl ketone, methyl isobutyl ketone, and the like. Examples of the alcohol solvent include methanol, ethanol, propanol, isopropanol, n-butanol, t-butanol and the like. Examples of nitrile solvents include acetonitrile, propionitrile, benzonitrile and the like. Examples of the ester solvent include ethyl acetate and butyl acetate. Examples of the carbonate solvent include ethylene carbonate and propylene carbonate. At least one of these may be used.

When a solvent is used, the amount used may be appropriately determined from the relationship between the viscosity of the entire system and the required stirring efficiency. In addition, in the case of bulk polymerization and polymerization performed in various solvents, even when the polymerization is stopped halfway, the monomer conversion rate at the point of stopping the reaction is the relationship between the viscosity of the entire system and the required stirring efficiency. It may be determined as appropriate.

The polymerization can be carried out in the range of 23 ° C to 200 ° C, preferably in the range of 50 ° C to 150 ° C. In order to produce a (meth) acrylic block copolymer by the above polymerization, a method of sequentially adding monomers, a method of polymerizing the next block using a pre-synthesized polymer as a polymer initiator, and polymerization separately And a method of bonding the obtained polymer by reaction. Any of these methods may be used, and they may be properly used according to the purpose. From the point of simplicity of the production process, the method by sequential addition of monomers is preferable, and in order to avoid the monomer of the previous block remaining and copolymerizing to the next block, it was synthesized in advance. A method of polymerizing the next block using a polymer as a polymer initiator is preferred.

Hereinafter, in the case of sequential addition of monomers, a case where the next block is polymerized using a polymer synthesized in advance as a polymer initiator will be described in detail, but the (meth) acrylic block copolymer of the present invention will be described. The manufacturing method is not limited.

In the case of sequential addition of monomers, it is desirable to charge the next monomer to be polymerized when the conversion rate of the previously charged monomer is 80 to 95%. When the polymerization is allowed to proceed until the conversion rate exceeds 95% (for example, up to 96 to 100%), the growth reaction of the polymer chain is stochastically suppressed. Further, since the polymer radicals are likely to react with each other, side reactions such as disproportionation, coupling, and chain transfer tend to occur. When the monomer to be polymerized next is charged when the conversion rate is less than 80% (for example, when it is 79% or less), the monomer previously charged for polymerization is the single monomer to be polymerized next. Mixing with a monomer and copolymerizing may cause a problem.

In this case, as the order of addition of the monomers, first, the acrylic monomer is first charged and polymerized, and then the methacrylic monomer is charged and polymerized. A method of charging and polymerizing an acrylic monomer after charging and polymerizing can be considered, but first a method of charging and polymerizing an acrylic monomer and then charging and polymerizing a methacrylic monomer Is preferable from the viewpoint of controlling the polymerization. This is because it is preferable to grow the methacrylic polymer block from the end of the acrylic polymer block.

As a method of polymerizing the next block using a polymer synthesized in advance as a polymer initiator, for example, at a desired point in the polymerization of the first block, the temperature is once lowered in the living state to stop the polymerization. There is a method in which the monomer of the second block is distilled off under reduced pressure, and then the monomer of the second block is added. When the third and subsequent blocks are to be polymerized, the same operation as that for the second block may be performed. In this method, at the time of polymerization of the second and subsequent blocks, it is possible to avoid copolymerization of the remaining monomers of the previous block.

Further, in this case, as a block polymerization sequence, first, a method of polymerizing an acrylic block after polymerizing the acrylic block, and a method of polymerizing an acrylic block after first polymerizing the methacrylic block However, the method of polymerizing the acrylic block after first polymerizing the acrylic block is preferable from the viewpoint of polymerization control. This is because it is preferable to grow the methacrylic polymer block from the end of the acrylic polymer block.

Here, how to determine the conversion rate of an acrylic monomer, a methacrylic monomer, etc. will be described. In order to obtain the conversion rate, a gas chromatograph (GC) method, a gravimetric method, or the like can be applied. In the GC method, the polymerization reaction solution is sampled as needed before and during the reaction, and GC measurement is performed. From the abundance ratio of the monomer and the internal standard substance previously added to the polymerization system, This is a method for obtaining the consumption rate. The advantage of this method is that each conversion rate can be determined independently even when a plurality of monomers are present in the system. The weight method is a method in which a polymerization reaction solution is sampled, the solid content concentration is obtained from the weight before drying and the weight after drying, and the conversion rate of the whole monomer is obtained. The advantage of this method is that the conversion can be easily determined. Among these methods, when a plurality of monomers are present in the system, for example, when an acrylic monomer is included as a copolymerization component of a methacrylic monomer, the GC method is used. preferable.

The reaction liquid obtained by the polymerization contains a mixture of a polymer and a metal complex, and is formed by adding a carboxylic acid group or an organic acid containing a sulfonic acid group to form a metal complex and a metal salt. The solid content is removed by filtering the metal complex, etc., followed by basic activated alumina, basic adsorbent, solid inorganic acid, anion exchange resin, acid remaining in the solution by cellulose anion exchanger adsorption treatment, etc. By removing impurities, a (meth) acrylic block copolymer solution can be obtained.

In the polymer solution thus obtained, the polymerization solvent and unreacted monomer are subsequently removed by an evaporation operation, and the (meth) acrylic block copolymer is isolated. As the evaporation method, a thin film evaporation method, a flash evaporation method, a horizontal evaporation method provided with an extrusion screw, or the like can be used. Since the (meth) acrylic block copolymer has adhesiveness, efficient evaporation is possible by combining the horizontal evaporation method with an extrusion screw alone or another evaporation method among the above evaporation methods.

<Production method of (meth) acrylic block copolymer (A)>
For the production of the (meth) acrylic block copolymer (A), the acid anhydride group precursor-containing (meth) acrylic block copolymer (A ′) produced above is used at a high temperature of 180 to 300 ° C. A method of heating is preferably used. At that time, the precursor containing an acid anhydride group (meth) acrylic block copolymer (A ′) may be heated under pressure in the state of the polymer solution, and the solvent is evaporated and removed from the polymer solution. The acid anhydride group precursor-containing (meth) acrylic block copolymer (A ′) may be directly heated and melted, but the reactivity to the acid anhydride group and the production From the standpoint of simplicity, it is preferable to directly heat-melt the anhydride-containing precursor-containing (meth) acrylic block copolymer (A ′). Furthermore, it is more preferable to melt-knead the acid anhydride group precursor-containing (meth) acrylic block copolymer (A ′).

The method of heating the precursor-containing (meth) acrylic block copolymer (A ′) of an acid anhydride group in the state of a polymer solution can be carried out in a pressure-resistant reaction vessel. In addition, as a method of heating the acid anhydride group precursor-containing (meth) acrylic block copolymer (A ′) while evaporating and removing the solvent from the polymer solution, a horizontal evaporation system equipped with an extrusion screw, etc. Can be used.

As a method of directly heating and melting the acid anhydride group precursor-containing (meth) acrylic block copolymer (A ′), a press machine, an injection molding machine, or the like can be used.

As a method of melt-kneading the precursor-containing (meth) acrylic block copolymer (A ′) of an acid anhydride group, it can be carried out in various apparatuses capable of performing heating and kneading simultaneously, For example, there are Banbury mixers, kneaders, single-screw or multi-screw extruders used for ordinary rubber processing. Although not particularly limited, an extruder is preferably used in terms of reactivity to an acid anhydride group and ease of production. When melt-kneading the precursor containing an acid anhydride group (meth) acrylic block copolymer (A ′), the melt-kneading time (or the residence time in the extruder when an extruder is used) is melt-kneaded. What is necessary is just to determine suitably according to the temperature to perform, screw structure, L / D (ratio of the screw effective length L and the screw diameter D), screw rotation speed, etc.

<Compound (B) containing two or more amino groups in one molecule>
The compound (B) having two or more amino groups in one molecule used as a crosslinking agent in the present invention is particularly limited as long as it is a compound having two or more primary or secondary amino groups in one molecule. However, from the viewpoint of reactivity with an acid anhydride group, a compound having a primary amino group is preferable, and a diamine having a primary amino group is preferable. Specific examples of the compound (B) containing two or more amino groups in one molecule include ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, tetramethylenediamine, pentamethylenediamine, hexamethylenediamine. , Trimethylhexamethylenediamine, dodecamethylenediamine, polyoxypropylene polyamine, 1,2-diaminopropane, bis (hexamethylene) triamine, tris (2-aminoethyl) amine, N, N′-dimethylethylenediamine, N, N ′ -Diethyl-1,3-propanediamine, N, N'-dibutyl-1,6-hexanediamine, N, N'-diethyl-2-butene-1,4-diamine, N, N'-diethyl-1, 4-diaminocyclohexane, molecular weight Aliphatic polyamines such as 200 to 1000 polyether polyamines (such as polyoxypropylenediamine having amino groups at both ends), cyclohexylenediamine, piperazine, isophoronediamine, 1,3-bisaminomethylcyclohexane, 1,4-bis Aminopropylpiperazine, 1,3-bisaminocyclohexane, di (aminodicyclohexyl) methane, 3,3′-dimethyldi (aminocyclohexyl) methane, 1-cyclohexylamino-3-aminopropane, 1,4-diaminocyclohexane, 1, 4-diaminocyclopentane, di (aminocyclohexyl) methane, di (aminocyclohexyl) sulfone, 1,3-di (aminocyclohexyl) propane, 4-isopropyl-1,2-diaminocyclohexane, 2,4-di Fats such as minocyclohexane, N, N′-diethyl-1,4-diaminocyclohexane, 3,3′-dimethyl-4,4′-diaminodicyclohexylmethane, 3-aminomethyl-3,3,5-trimethylcyclohexylamine Cyclic polyamines, melamine, benzidine, o-phenylenediamine, m-phenylenediamine, p-phenylenediamine, 4,4′-diaminodiphenylmethane, 4,4′-diaminodiphenylsulfone, 4,4′-diaminodiphenylether, 2 And aromatic polyamine compounds such as 1,4-diaminodiphenylamine, 1,5-diaminonaphthalene, 1,8-diaminonaphthalene, and 2,4-diaminotoluene.

At least one of these can be used. Among these, those having a boiling point of 100 ° C. or higher are preferable, and those having a boiling point of 150 ° C. or higher are more preferable in view of availability, cost, and handling during the reaction. Moreover, 1-20 are preferable and, as for carbon number of a compound (B), the thing of 1-10 is more preferable. Moreover, it is preferable to use what was excellent in compatibility with the (meth) acrylic block copolymer (A). Specifically, aliphatic polyamines and alicyclic polyamines are preferable, aliphatic polyamines are more preferable, and hexamethylenediamine is particularly preferable.

The number of amino groups contained in the compound (B) containing two or more amino groups in one molecule to be used may be appropriately determined according to the balance between hardness and mechanical strength of the elastomer to be obtained and compression set characteristics. Regarding the compounding amount of these compounds (B), the ratio of the number of moles of amino groups in compound (B) to the number of moles of acid anhydride groups (a1) in (meth) acrylic block copolymer (A) is as follows. The range of 0.01 to 10 is preferable, and the range of 0.05 to 10 is more preferable. If the blending amount of the compound (B) containing two or more amino groups in one molecule exceeds 10, the mechanical strength of the thermoplastic elastomer obtained tends to be reduced, and if it is less than 0.01, In some cases, the crosslinking reactivity of the resulting thermoplastic elastomer is lowered.

<Thermoplastic resin (C)>
The thermoplastic resin (C) that can be used in the present invention is not particularly limited, and examples thereof include polyvinyl chloride resins, polyethylene resins, polypropylene resins, cyclic olefin copolymer resins, polymethyl methacrylate resins, and polystyrene resins. , Polyphenylene ether resin, polycarbonate resin, polyester resin, polyamide resin, polyacetal resin, polyphenylene sulfide resin, polysulfone resin, polyimide resin, polyetherimide resin, polyetherketone resin, polyetheretherketone resin, polyamideimide resin And 70 to 100% by weight of at least one vinyl monomer selected from the group consisting of an aromatic alkenyl compound, a vinyl cyanide compound, and a (meth) acrylic acid ester; Examples thereof include homopolymers and copolymers that are copolymerizable with other monomers, for example, obtained by polymerizing 30 to 0% by weight of other vinyl monomers such as ethylene, propylene, and vinyl acetate. . At least one of these can be used.

More specifically, as the polyvinyl chloride resin, for example, polyvinyl chloride homopolymers, vinyl chloride-vinyl acetate copolymers, vinyl chloride-vinyl acetate-maleic anhydride copolymers having various polymerization degrees, Polyvinyl chloride copolymer such as vinyl chloride-ethylene copolymer, vinyl chloride-propylene copolymer; alloy of polyvinyl chloride and ethylene-vinyl acetate copolymer, alloy of polyvinyl chloride and chlorinated polyethylene, Polyvinyl chloride alloys such as alloys of polyvinyl chloride and acrylic copolymers, alloys of polyvinyl chloride and polyurethane, etc .; functionalized polyvinyl chlorides such as polyvinyl chloride / filler composites and post-chlorinated polyvinyl chloride , Polyvinylidene chloride homopolymer, vinylidene chloride-vinyl chloride copolymer, vinylidene chloride-acrylonitrile copolymer Body, vinylidene chloride - such as polyvinylidene chloride copolymers such as acrylic acid ester copolymer.

Examples of the polyethylene resin include polyethylene resins such as low density polyethylene, high density polyethylene, linear low density polyethylene, and ultrahigh molecular weight polyethylene; ethylene-vinyl acetate copolymer, ethylene-methyl acrylate copolymer, Ethylene-ethyl acrylate copolymer, ethylene-methyl methacrylate copolymer, ethylene-ethyl acrylate-glycidyl methacrylate copolymer, ethylene-vinyl acetate-glycidyl methacrylate copolymer, ethylene-acrylic acid copolymer, ethylene and acrylic Copolymer with metal salt of acid or methacrylic acid, maleic anhydride modified polyethylene, maleic anhydride modified ethylene-ethyl acrylate copolymer, ethylene-dimethylaminomethyl methacrylate copolymer, ethylene - vinyl alcohol copolymer, ethylene - can be exemplified a copolymer of ethylene and a polar monomer such as ethylene oxide adducts of vinyl alcohol copolymer.

Examples of the polypropylene resin include homoisotactic polypropylene, isotactic polypropylene random copolymer containing ethylene or 1-butene, isotactic polypropylene block copolymer containing ethylene propylene, and Ziegler-Natta catalyst isoform. Examples thereof include polypropylenes such as tactic polypropylene, metallocene catalyst-based isotactic polypropylene, metallocene catalyst-based syndiotactic polypropylene, and atactic polypropylene; functionalized polypropylene such as polypropylene / filler composite, chlorinated polypropylene, and maleic acid-modified polypropylene.

The cyclic olefin copolymer resin is not particularly limited as long as it contains a cyclic olefin, for example, a monomer unit derived from cyclopentadiene. For example, ARTON (manufactured by JSR Corporation), ZEONEX (Japan) Zeon Co., Ltd.), a copolymer of cyclic olefin and ethylene or propylene.

The polymethyl methacrylate resin is not particularly limited as long as it is a resin mainly composed of methyl methacrylate, and may be a polymethyl methacrylate resin in which α-methylstyrene, maleic anhydride, or the like is copolymerized. it can.

Examples of the polystyrene resin include polystyrene homopolymer, syndiotactic polystyrene, and the like.

Further, 70 to 100% by weight of at least one vinyl monomer selected from the group consisting of an aromatic alkenyl compound, a vinyl cyanide compound and a (meth) acrylic acid ester, and these vinyl monomers As a homopolymer or copolymer that can be polymerized, for example, obtained by polymerizing 0 to 30% by weight of other vinyl monomers such as ethylene, propylene, and vinyl acetate, for example, acrylonitrile-styrene copolymer Resins, acrylonitrile-butyl acrylate-styrene copolymers, acrylonitrile-ethylene / propylene-styrene copolymers, acrylonitrile-chlorinated polyethylene-styrene copolymers, and other acrylonitrile-styrene copolymer resins; methyl methacrylate-styrene Examples thereof include copolymer resins.

Examples of the polyphenylene ether resin include polyphenylene ether homopolymers; alloys of polyphenylene ether and polystyrene, alloys of polyphenylene ether and polyamide, and alloys of polyphenylene ether and polybutylene terephthalate.

Polycarbonate resins include polycarbonates such as bisphenol A type aromatic polycarbonate; polycarbonate alloys such as alloys of polycarbonate and polybutylene terephthalate, alloys of polycarbonate and polyarylate, and alloys of polycarbonate and polymethyl methacrylate. It is done.

Examples of polyester resins include aliphatic polyesters such as polyglycolic acid, polylactic acid, polycaprolactone, and polyethylene succinate; polyethylene terephthalate, polytrimethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, and polycyclohexanedimethylene terephthalate. Semi-aromatic polyesters such as ethylene terephthalate / cyclohexanedimethylene terephthalate copolymer and thermotropic liquid crystal polymer type 2; amorphous polyarylate, thermotropic liquid crystal polymer type 1 and thermotropic liquid crystal polymer type 2 Aromatic polyesters and ester elastomers can be mentioned.

Examples of polyamide resins include ring-opening polymerization aliphatic polyamides such as PA6 and PA12; polycondensation polyamides such as PA66, PA46, PA610, PA612, and PA11; MXD6, PA6T, PA9T, PA6T / 66, PA6T / 6, semi-aromatic polyamides such as amorphous PA; wholly aromatic polyamides such as poly (p-phenylene terephthalamide), poly (m-phenylene terephthalamide), poly (m-phenylene isophthalamide), amide elastomers, etc. can give.

Examples of the polyacetal resin include a polyacetal homopolymer and a copolymer of formaldehyde and trioxane. In the present invention, the thermoplastic resin (C) is not limited to these, and various thermoplastic resins can be widely used, such as styrene elastomers, olefin elastomers, vinyl chloride elastomers, urethane elastomers, and the like. These thermoplastic elastomers can also be used.

Of these various thermoplastic resins, those having a softening temperature of 100 ° C. or higher and a melting temperature of 300 ° C. or lower are preferable. Among them, polymethyl methacrylate resins, polyolefin resins, polyester resins, polyamide resins, polycarbonates Resin is preferable, and polyester resin and polyamide resin are more preferable in terms of compatibility with the (meth) acrylic block copolymer (A), oil resistance and heat resistance of the resulting thermoplastic elastomer. In particular, from the viewpoint of compatibility with the (meth) acrylic block copolymer (A), a polyamide resin having reactivity with the acid anhydride group (a1) is preferable. For example, PA6 (polycaproamide), PA12 ( Polydodecanamide) and PA612.

The blending amount of these thermoplastic resins (C) is preferably 5 to 150 parts by weight and more preferably 10 to 100 parts by weight with respect to 100 parts by weight of the (meth) acrylic block copolymer (A). When the blending amount of the thermoplastic resin (C) is larger than 150 parts by weight, the rubber elasticity of the obtained thermoplastic elastomer may be lowered. If the thermoplastic resin (C) is less than 5 parts by weight, the moldability and mechanical strength of the resulting thermoplastic elastomer may be lowered.

<Plasticizer (D)>
A plasticizer is added to the thermoplastic elastomer of the present invention in order to impart oil resistance and fuel oil resistance of the thermoplastic elastomer composition.
Examples of the plasticizer include plasticizers that are usually blended in thermoplastic resins and rubbers; softeners such as process oils; oligomers; oils such as animal oils and vegetable oils; petroleum fractions such as kerosene, light oil, heavy oil, and naphtha. However, it is not limited to them. Examples of the softening agent include process oil, and more specifically, petroleum-based process oils such as paraffin oil; naphthenic process oil; aromatic process oil and the like. Examples of the plasticizer include dimethyl phthalate, diethyl phthalate, di-n-butyl phthalate, di (2-ethylhexyl) phthalate, diheptyl phthalate, diisodecyl phthalate, di-n-octyl phthalate, and phthalic acid. Phthalic acid derivatives such as diisononyl, ditridecyl phthalate, octyldecyl phthalate, butyl benzyl phthalate, dicyclohexyl phthalate, phthalate-β-hydroxyethyl-2-ethylhexyl; isophthalic acid derivatives such as dimethyl isophthalate; di- (2 Tetrahydrophthalic acid derivatives such as -ethylhexyl) tetrahydrophthalic acid; dimethyl adipate, dibutyl adipate, di-n-hexyl adipate, di- (2-ethylhexyl) adipate, isononyl adipate, diisodecyl adipate, adipate Adipic acid derivatives such as dibutyl diglycolate; azelaic acid derivatives such as di-2-ethylhexyl azelate; sebacic acid derivatives such as dibutyl sebacate; dodecane-2-acid derivatives; dibutyl maleate, di-2-ethylhexyl maleate Maleic acid derivatives such as: fumaric acid derivatives such as dibutyl fumarate; 2-ethylhexyl o- or p-hydroxybenzoate, hexyldecyl o- or p-hydroxybenzoate, 2-ethyldecyl o- or p-hydroxybenzoate, octyloctyl o- or p-hydroxybenzoate, decyldodecyl o- or p-hydroxybenzoate, methyl o- or p-hydroxybenzoate, butyl o- or p-hydroxybenzoate, o- or p-hydroxybenzoic acid Hexyl, o- or Hydroxybenzoates such as n-octyl p-hydroxybenzoate, o- or decyl p-hydroxybenzoate, o- or dodecyl p-hydroxybenzoate; trimellitic acid derivatives such as tris-2-ethylhexyl trimellitic acid; pyromellitic Citric acid derivatives such as acetyltributyl citrate; itaconic acid derivatives; oleic acid derivatives; ricinoleic acid derivatives; stearic acid derivatives; other fatty acid derivatives; sulfonic acid derivatives; phosphoric acid derivatives; glutaric acid derivatives; Polyester plasticizers that are polymers of dibasic acids such as phthalic acid and glycols and monohydric alcohols, glycol derivatives, glycerin derivatives, paraffin derivatives such as chlorinated paraffin, and epoxy derivative polyester polymerization type Agents, polyether polymerization type plasticizers, carbonate derivatives such as ethylene carbonate and propylene carbonate, N-alkylbenzenesulfones such as N-propylbenzenesulfonamide, Nn-butylbenzenesulfonamide, N-2-ethylhexylbenzenesulfonamide Amides; N-butyl-N-ethyl-o- or N-butyl-N-ethyl-p-toluenesulfonamide, N-ethyl-N-2-ethylhexyl-o- or N-ethyl-N-2-ethylhexyl -N-alkyltoluenesulfonamides such as p-toluenesulfonamide; vinyl polymers obtained by polymerizing vinyl monomers such as acrylic plasticizers by various methods. In the present invention, the plasticizer is not limited to these, and various plasticizers can be used, and those widely marketed as rubber or thermoplastic resin plasticizers can also be used. Commercially available plasticizers include Thiocol TP (manufactured by Morton), Adekasizer O-130P, C-79, UL-100, P-200, RS-735 (Asahi Denka Co., Ltd.), Sunsocizer N -400 (manufactured by Shin Nippon Rika Co., Ltd.), BM-4 (manufactured by Daihachi Chemical Industry Co., Ltd.), EHPB (manufactured by Ueno Pharmaceutical Co., Ltd.), Exepar (manufactured by Kao Corporation), UP-1000 (Toa) Synthetic Chemical Co., Ltd.). Examples of vegetable oils include castor oil, cottonseed oil, linseed oil, rapeseed oil, soybean oil, palm oil, palm oil, peanut oil, pine oil, tall oil and the like.

In the above, it is preferable to use a material having excellent affinity with the (meth) acrylic block copolymer (A) or the thermoplastic resin (C). Although not particularly limited, adipic acid derivatives, phthalic acid derivatives, glutaric acid derivatives, trimellitic acid derivatives, pyromellitic acid derivatives, polyester plasticizers, glycerin derivatives, epoxy derivatives, which are low volatility and low heat loss plasticizers. Vinyl polymers obtained by polymerizing vinyl monomers including polyester polymerization plasticizers, polyether polymerization plasticizers, acrylic plasticizers by various methods, hydroxybenzoates, N- Polymer plasticizers such as alkylbenzenesulfonamides and N-alkyltoluenesulfonamides are preferably used. For example, when a polyamide resin is used for the thermoplastic resin (C), phthalic acid derivatives, hydroxybenzoic acid esters, etc. in terms of flexibility, hardness adjustment, oil resistance, heat resistance, and fuel oil resistance of the resulting thermoplastic elastomer. N-alkylbenzenesulfonamides and N-alkyltoluenesulfonamides are preferably used.

The above plasticizers may be used alone or in combination. The amount of the plasticizer (D) is preferably 1 to 300 parts by weight, more preferably 1 to 200 parts by weight, with respect to 100 parts by weight of the (meth) acrylic block copolymer (A). More preferably, 100 parts by weight. If the blending amount exceeds 300 parts by weight, the heat resistance and mechanical strength of the resulting thermoplastic elastomer may be lowered, and if it is less than 1 part by weight, the oil resistance and fuel oil resistance may be lowered.

The thermoplastic elastomer composition of the present invention comprises the above (meth) acrylic block copolymer (A), a compound (B) containing two or more amino groups in one molecule, a thermoplastic resin (C) and a plastic. In addition to the agent (D), stabilizers, lubricants, flame retardants, pigments, fillers, reinforcing agents, tackifiers and the like can be appropriately blended as necessary. Specifically, stabilizers such as hindered phenol, hindered amine and dibutyltin maleate; lubricants such as polyethylene wax, polypropylene wax and montanic acid wax; flame retardants such as decabromobiphenyl and decabromobiphenyl ether; titanium oxide, sulfide Zinc, zinc oxide and other pigments; carbon black, silica, glass fiber, asbestos, wollastonite, mica, talc, calcium carbonate and other fillers, reinforcing agents; coumarone / indene resin, phenolic resin, terpene resin, high styrene resin And tackifiers such as petroleum hydrocarbons (for example, dicyclopentadiene resin, aliphatic cyclic hydrocarbon resin, unsaturated hydrocarbon resin, etc.), polybutene, rosin derivatives, and the like.

Furthermore, in order to further improve the compatibility between the (meth) acrylic block copolymer (A) and the thermoplastic resin (C), various graft polymers and block polymers may be added as a compatibilizing agent. As compatibilizers, Kraton series (manufactured by Shell Japan), Tuftec series (manufactured by Asahi Kasei Kogyo Co., Ltd.), Dynalon (manufactured by Nippon Synthetic Rubber Co., Ltd.), Epofriend (manufactured by Daicel Chemical Industries, Ltd.), Septon (Kuraray Co., Ltd.), Nofaloy (Nippon Yushi Co., Ltd.), Lexpearl (Nippon Polyolefin Co., Ltd.), Bond First (Sumitomo Chemical Co., Ltd.), Bondine (Sumitomo Chemical Co., Ltd.) ), Admer (Mitsui Chemicals Co., Ltd.), Umex (Sanyo Chemical Industries Co., Ltd.), VMX (Mitsubishi Chemical Co., Ltd.), Modiper (Nippon Yushi Co., Ltd.), Staphyroid (Takeda Pharmaceutical Co., Ltd.) And commercial products such as Kane Ace (manufactured by Kaneka Chemical Co., Ltd.) and Reseta (manufactured by Toa Gosei Co., Ltd.). These can be appropriately selected according to the (meth) acrylic block copolymer (A) and the thermoplastic resin (C) to be used.

<Method for producing thermoplastic elastomer composition>
The thermoplastic elastomer composition of the present invention comprises two compositions each composed of the (meth) acrylic block copolymer (A), the thermoplastic resin (C) and the plasticizer (D) prepared above. It is produced by substantially reacting with the above compound (B) containing an amino group. Although not particularly limited, more preferably, two or more amino groups are contained in one molecule while melting and kneading the composition containing the (meth) acrylic block copolymer (A) and the thermoplastic resin (C) at a high temperature. In addition to the plasticizer (D) and further stabilizers, lubricants, flame retardants, pigments, fillers, reinforcing materials, lubricants, tackifiers, compatibilizers, etc. It is manufactured by adding these components and carrying out dynamic crosslinking.

As the kneader used for the production of the composition, various apparatuses capable of performing heating and kneading at the same time can be used. For example, a Banbury mixer, a kneader, a single screw or a multi-screw used for ordinary rubber processing can be used. Extruder etc. Furthermore, if necessary, the composition can be molded using a press, an injection molding machine or the like. The kneading temperature for producing the composition is preferably 100 to 300 ° C, more preferably 150 to 250 ° C.

The (meth) acrylic block copolymer (A) obtained in the present invention (A), a compound (B) containing two or more amino groups in one molecule, a thermoplastic resin (C) and a plasticizer (D) are combined. The thermoplastic elastomer composition obtained by dynamically cross-linking the composition has improved oil resistance, heat resistance, mechanical properties, etc. while maintaining the inherent properties of the (meth) acrylic block copolymer. It can be more suitably used as an automobile or an electric / electronic component. Specifically, the types are oil seals, various oil seals such as reciprocating oil seals, various packings such as gland packing, lip packing, squeeze packing, constant velocity joint boots, strut boots, rack and pinion boots, brakes Various boots such as booster boots, steering ball joint boots, fuel hoses, gasoline hoses, air conditioning hoses, brake hoses, air hoses, air duct hoses, air cleaner hoses, suspension dust covers, suspension tie rods Various dust covers such as dust covers for stabilizers, dust covers for stabilizers and die rods, resin intake manifold gaskets, gaskets for throttle bodies, powers Alling vane pump gasket, head cover gasket, water heater self-contained pump gasket, filter gasket, piping joint (ABS & HBB) gasket, HDD top cover gasket, HDD connector gasket, cylinder head gasket combined with metal, car cooler Various gaskets such as compressor gaskets, gaskets around the engine, AT separate plates, general-purpose gaskets (industrial sewing machines, nailing machines, etc.), needle valves, plunger valves, water / gas valves, brake valves, drinking valves, aluminum electrolysis Various valves such as safety valves for condensers, vacuum boosters, water / gas diaphragms, seal washers, bore plugs, high-precision stoppers, etc. Plug tube seal, the injection pipe seal, oil receiver, a brake drum seal, shielding seals, plug seals, connectors seal, and the like precision seal rubber such as keyless entry cover. In addition, various weather strips such as door weather strips for automobiles, seal products such as trunk seals and glass run channels can be listed.

The molding of the product is performed by molding the thermoplastic elastomer composition by any molding method such as extrusion molding, compression molding, blow molding, calendar molding, vacuum molding, foam molding, injection molding, injection blow, and the like. It can be carried out.

A composition comprising the (meth) acrylic block copolymer (A), a compound (B) containing two or more amino groups in one molecule, a thermoplastic resin (C) and a plasticizer (D) is heated. Dynamically-crosslinked thermoplastic elastomer compositions are used in hoses, sheets, film materials, vibration dampers, adhesives in fields such as packaging materials, construction, civil engineering materials, and miscellaneous goods in addition to automobiles and electrical / electronic components It can also be used widely and suitably as a base polymer, a resin modifier, and the like.

EXAMPLES Next, although this invention is demonstrated further in detail based on an Example, this invention is not limited only to these Examples.
In the examples, BA, MMA, and TBA represent n-butyl acrylate, methyl methacrylate, and t-butyl acrylate, respectively. “Co” represents a bond by random copolymerization, and the abbreviation “b” represents a bond by block copolymerization.

<Test method>
(Molecular weight)
The molecular weight shown in the present example was measured by the GPC analyzer shown below, and GPC measurement using a polystyrene gel column was performed using chloroform as a mobile phase to determine the molecular weight in terms of polystyrene. GPC measurement was performed with a GPC analyzer (system: GPC system manufactured by Waters, column: Shodex K-804 (polystyrene gel) manufactured by Showa Denko KK). The molecular weight in terms of polystyrene was determined using chloroform as the mobile phase.

(hardness)
According to JIS K6253, the hardness at 23 ° C. (immediately after, JIS A) was measured with a type A durometer.

(Mechanical strength)
Measurements were made using an autograph AG-10TB model manufactured by Shimadzu Corporation, applying the method described in JIS K7113. The measurement was performed at n = 3, and the average value of the strength (MPa) and elongation (%) when the test piece was broken and the elastic modulus (MPa) was adopted. A test piece having a shape of 2 (1/3) shape and a thickness of about 2 mm was used. The test was conducted at 23 ° C. and a test speed of 500 mm / min. In principle, the test piece was conditioned for 48 hours or more at a temperature of 23 ± 2 ° C. and a relative humidity of 50 ± 5% before the test.

(Oil resistance)
In accordance with ASTM D638, ASTM oil no. 3 was immersed for 72 hours, and the weight change rate (% by weight) was determined. In addition, for the appearance evaluation after the test, the shape of the molded body before and after the test was observed, and judged as ◯: shape maintenance, x: deformation.

(Heat-resistant)
This was done by comparing the flow start temperatures. The flow starting temperature was 1 mm in inner diameter at a load of 60 kgf / cm ² with a composition heated at a heating rate of 5 ° C./min using a Koka-type flow tester CFT-500C manufactured by Shimadzu Corporation. When the resin was extruded from a nozzle having a length of 10 mm, the temperature was set to a temperature at which the resin extrusion piston of the flow tester clearly began to descend (indicated as Tfb in this measuring device).

(Fuel resistance)
In accordance with JIS K6258, the molded product of the composition was immersed in test fuel oil C (isooctane / toluene = 50/50 (v / v)) maintained at 23 ° C. for 70 hours to obtain the volume change rate (%). The fuel oil resistance evaluation was judged as ◯: 70% or less and x: greater than 70% from the volume change rate before and after the test.

Production Example 1
Synthesis of MMA-b-BA-b-MMA type block copolymer (BA / MMA = 70/30 wt%) (hereinafter abbreviated as MBAM) After purging the inside of the polymerization vessel of a 5 L separable flask with nitrogen, 11.3 g (78.5 mmol) of copper chloride was weighed, and 180 mL of acetonitrile (dried with molecular sieves and then bubbled with nitrogen) was added. After heating and stirring at 70 ° C. for 5 minutes, the mixture was cooled again to room temperature, and initiator 5.7 g (15.7 mmol) of diethyl 2,5-dibromoadipate and 804.6 g (900.0 mL) of n-butyl acrylate were added. added. The mixture was heated and stirred at 80 ° C., and 1.6 mL (7.9 mmol) of ligand diethylenetriamine was added to initiate polymerization. About every 0.2 mL of the polymerization solution was sampled from the polymerization solution for sampling at regular intervals from the start of polymerization, and the conversion of n-butyl acrylate was determined by gas chromatogram analysis of the sampling solution. The polymerization rate was controlled by adding triamine as needed. When the conversion rate of n-butyl acrylate was 95%, methyl methacrylate, 345.7 g (369.3 mL), copper chloride, 7.8 g (78.5 mmol), diethylenetriamine, 1.6 mL (7.9 mmol) , 1107.9 mL of toluene (dried with molecular sieves and then bubbled with nitrogen) was added. Similarly, the conversion rate of methyl methacrylate was determined. When the conversion rate of methyl methacrylate was 85% and the conversion rate of n-butyl acrylate was 98%, 1500 mL of toluene was added and the reactor was cooled in a water bath to complete the reaction. During the reaction, the polymerization solution was always green. The reaction solution was diluted with 4000 mL of toluene, 22.1 g of p-toluenesulfonic acid monohydrate was added, and the mixture was stirred at room temperature for 3 hours. The precipitated insoluble part was removed by filtration with a Kiriyama funnel, and then 9.7 g of the adsorbent Kyoward 500SH was added to the polymer solution, followed by further stirring at room temperature for 3 hours. The adsorbent was filtered with a Kiriyama funnel to obtain a colorless and transparent polymer solution. This solution was dried to remove the solvent and residual monomer to obtain the target MBAM. When GPC analysis of the obtained MBAM was performed, the number average molecular weight Mn was 119200, and the molecular weight distribution Mw / Mn was 1.51. Moreover, it was BA / MMA = 72/28 (weight%) when the compositional analysis by NMR was conducted.

Production Example 2
MMA-b- (BA-co-TBA) -b-MMA (BA / TBA = 97.5 / 2.5 mol%, (BA-co-TBA) / MMA = 70/30 wt%) type (meth) acrylic Synthesis of System Block Copolymer (hereinafter referred to as 2.5STBA7) After the inside of a 5 L separable flask was purged with nitrogen, 11.3 g (78.4 mmol) of copper bromide was weighed and acetonitrile (nitrogen) 180 mL was added. After heating and stirring at 70 ° C. for 30 minutes, 5.65 g (15.7 mmol) of diethyl 2,5-dibromoadipate initiator, 877 mL (6.12 mol) of BA, and 22.9 mL (0.16 mol) of TBA were added. . The mixture was heated and stirred at 85 ° C., and 1.64 mL (7.8 mmol) of ligand diethylenetriamine was added to initiate polymerization. When the conversion rate of BA was 95% and the conversion rate of TBA was 100%, 369 mL (3.45 mol) of MMA was added. The reaction was terminated when the MMA conversion was 64%. Otherwise, the same production as in Production Example 1 was carried out to obtain the desired (meth) acrylic block copolymer 2.5STBA7.
When the GPC analysis of the obtained (meth) acrylic block copolymer 2.5STBA7 was conducted, the number average molecular weight Mn was 97900, and the molecular weight distribution Mw / Mn was 1.44.

Example 1
Laboplast mill (Toyo) in which 45 g of (meth) acrylic block copolymer 2.5STBA7 produced in Production Example 2 and 0.23 g of Irganox 1010 (manufactured by Ciba Specialty Chemicals) were set at 240 ° C. The resulting acid anhydride group-containing (meth) acrylic block copolymer (the obtained polymer is described as 2.5SANBA7) was obtained by melt-kneading at 100 rpm for 20 minutes using a Seiki Co., Ltd. . The obtained 2.5 SANBA7 and polyamide; PA (UBE nylon 3012U: Ube Industries, Ltd.), Irganox 1010 (Ciba Specialty Chemicals, Inc.) at a ratio shown in Table 1 at 190 ° C It melt-kneaded using the set Laboplast mill (made by Toyo Seiki Co., Ltd.). Further, hexamethylene diamine (manufactured by Tokyo Chemical Industry Co., Ltd.) was added at the ratio shown in Table 1 and melt kneaded to advance the reaction (dynamic crosslinking). Thereafter, Sansosizer N400 (manufactured by Shin Nippon Rika Co., Ltd.) was added at the ratio shown in Table 1, and melt kneaded at 190 ° C. The heat resistance of the obtained sample was measured. The obtained sample was hot press molded at a set temperature of 190 ° C. to obtain a cylindrical molded body having a diameter of 30 mm and a thickness of 12 mm. The hardness of these molded bodies was measured. Similarly, hot press molding was performed at a set temperature of 190 ° C. to obtain a sheet-like molded body having a thickness of 2 mm. These sheets were measured for mechanical strength, oil resistance, and fuel oil resistance.

Example 2
2.5 SANBA7 obtained by the same method as in Example 1 and polyamide; PA (UBE nylon 3012U: manufactured by Ube Industries, Ltd.), Irganox 1010 (produced by Ciba Specialty Chemicals, Inc.) are shown in Table 1. The mixture was melt-kneaded using a lab plast mill (manufactured by Toyo Seiki Co., Ltd.) set at 190 ° C. at the rate shown in FIG. Further, hexamethylene diamine (manufactured by Tokyo Chemical Industry Co., Ltd.) was added at the ratio shown in Table 1 and melt kneaded to advance the reaction (dynamic crosslinking). Thereafter, 2-ethylhexyl p-hydroxybenzoate (manufactured by Tokyo Chemical Industry Co., Ltd.) was further added at the ratio shown in Table 1, and melt-kneaded at 190 ° C. The heat resistance of the obtained sample was measured. The obtained sample was hot press molded at a set temperature of 190 ° C. to obtain a cylindrical molded body having a diameter of 30 mm and a thickness of 12 mm. The hardness of these molded bodies was measured. Similarly, hot press molding was performed at a set temperature of 190 ° C. to obtain a sheet-like molded body having a thickness of 2 mm. These sheets were measured for mechanical strength, oil resistance, and fuel oil resistance.

Example 3
2.5 SANBA7 obtained by the same method as in Example 1 and polyamide; PA (UBE nylon 3012U: manufactured by Ube Industries, Ltd.), Irganox 1010 (produced by Ciba Specialty Chemicals, Inc.) are shown in Table 1. The mixture was melt-kneaded using a lab plast mill (manufactured by Toyo Seiki Co., Ltd.) set at 190 ° C. at the rate shown in FIG. Further, hexamethylene diamine (manufactured by Tokyo Chemical Industry Co., Ltd.) was added at the ratio shown in Table 1 and melt kneaded to advance the reaction (dynamic crosslinking). Thereafter, Sansosizer N400 (manufactured by Shin Nippon Rika Co., Ltd.) was added at the ratio shown in Table 1, and melt kneaded at 190 ° C. The heat resistance of the obtained sample was measured. The obtained sample was hot press molded at a set temperature of 190 ° C. to obtain a cylindrical molded body having a diameter of 30 mm and a thickness of 12 mm. The hardness of these molded bodies was measured. Similarly, hot press molding was performed at a set temperature of 190 ° C. to obtain a sheet-like molded body having a thickness of 2 mm. These sheets were measured for mechanical strength, oil resistance, and fuel oil resistance.

Example 4
2.5 SANBA7 obtained by the same method as in Example 1 and polyamide; PA (UBE nylon 3012U: manufactured by Ube Industries, Ltd.), Irganox 1010 (produced by Ciba Specialty Chemicals, Inc.) are shown in Table 1. The mixture was melt-kneaded using a lab plast mill (manufactured by Toyo Seiki Co., Ltd.) set at 190 ° C. at the rate shown in FIG. Further, hexamethylene diamine (manufactured by Tokyo Chemical Industry Co., Ltd.) was added at the ratio shown in Table 1 and melt kneaded to advance the reaction (dynamic crosslinking). Thereafter, PA was further added at a rate shown in Table 1, and melt-kneaded at 190 ° C. Subsequently, Nn-butylbenzenesulfonamide (manufactured by Daihachi Chemical Industry Co., Ltd.) was added at the ratio shown in Table 1, and melt-kneaded at 190 ° C. The heat resistance of the obtained sample was measured. The obtained sample was hot press molded at a set temperature of 190 ° C. to obtain a cylindrical molded body having a diameter of 30 mm and a thickness of 12 mm. The hardness of these molded bodies was measured. Similarly, hot press molding was performed at a set temperature of 190 ° C. to obtain a sheet-like molded body having a thickness of 2 mm. These sheets were measured for mechanical strength, oil resistance, and fuel oil resistance.

Comparative Example 1
Laboplast mill (Toyo Seiki Co., Ltd.) in which MBAM and Irganox 1010 (manufactured by Ciba Specialty Chemicals Co., Ltd.) produced in Production Example 1 were set at 190 ° C. at a screw rotation speed of 50 rpm at the ratio shown in Table 1. )) To obtain a sample. The heat resistance of the obtained sample was measured. The obtained sample was hot press molded at a set temperature of 190 ° C. to obtain a cylindrical molded body having a diameter of 30 mm and a thickness of 12 mm. The hardness of these molded bodies was measured. Similarly, hot press molding was performed at a set temperature of 190 ° C. to obtain a sheet-like molded body having a thickness of 2 mm. These sheets were measured for mechanical strength, oil resistance, and fuel oil resistance.
It can be seen that MBAM alone has insufficient mechanical strength, oil resistance, heat resistance and fuel oil resistance.

Comparative Example 2
MBAM and polyamide manufactured in Production Example 1; PA (UBE nylon 3012U: manufactured by Ube Industries), Irganox 1010 (manufactured by Ciba Specialty Chemicals) at the ratio shown in Table 1 The mixture was melt kneaded using a Laboplast mill (manufactured by Toyo Seiki Co., Ltd.) set at 190 rpm at 100 rpm. The heat resistance of the obtained sample was measured. The obtained sample was hot press molded at a set temperature of 190 ° C. to obtain a cylindrical molded body having a diameter of 30 mm and a thickness of 12 mm. The hardness of these molded bodies was measured. Similarly, hot press molding was performed at a set temperature of 190 ° C. to obtain a sheet-like molded body having a thickness of 2 mm. These sheets were measured for mechanical strength, oil resistance, and fuel oil resistance.
It can be seen that a sample obtained by only melt kneading MBAM and PA has insufficient mechanical strength, oil resistance, heat resistance and fuel oil resistance.

Comparative Example 3
Laboplast mill (Toyo) in which 45 g of (meth) acrylic block copolymer 2.5STBA7 produced in Production Example 2 and 0.23 g of Irganox 1010 (manufactured by Ciba Specialty Chemicals) were set at 240 ° C. The resulting acid anhydride group-containing (meth) acrylic block copolymer (the obtained polymer is described as 2.5SANBA7) was obtained by melt-kneading at 100 rpm for 20 minutes using a Seiki Co., Ltd. . Laboplast mill in which the obtained 2.5SANBA7 and polyamide; PA (UBE nylon 3012U: manufactured by Ube Industries), Irganox 1010 (manufactured by Ciba Geigy) were set at 190 ° C. at the ratio shown in Table 1. The mixture was melt kneaded using Toyo Seiki Co., Ltd. Further, hexamethylene diamine (manufactured by Tokyo Chemical Industry Co., Ltd.) was added at the ratio shown in Table 1 and melt kneaded to advance the reaction (dynamic crosslinking). The heat resistance of the obtained sample was measured. The obtained sample was hot press molded at a set temperature of 190 ° C. to obtain a cylindrical molded body having a diameter of 30 mm and a thickness of 12 mm. The hardness of these molded bodies was measured. Similarly, hot press molding was performed at a set temperature of 190 ° C. to obtain a sheet-like molded body having a thickness of 2 mm. These sheets were measured for mechanical strength, oil resistance, and fuel oil resistance.
It can be seen that the sample obtained without adding the plasticizer has insufficient fuel oil resistance.

Comparative Example 4
It was melt-kneaded using a Laboplast mill (manufactured by Toyo Seiki Co., Ltd.) in which Dilast (701-80W180: manufactured by AES Japan Co., Ltd.) was set to 190 ° C. The heat resistance of the obtained sample was measured. The obtained sample was hot press molded at a set temperature of 190 ° C. to obtain a cylindrical molded body having a diameter of 30 mm and a thickness of 12 mm. The hardness of these molded bodies was measured. Similarly, hot press molding was performed at a set temperature of 190 ° C. to obtain a sheet-like molded body having a thickness of 2 mm. These sheets were measured for mechanical strength, oil resistance, and fuel oil resistance. It can be seen that dilast, which is an olefinic thermoplastic elastomer, has insufficient oil resistance.

As apparent from Table 1 (Examples 1 to 4 and Comparative Examples 1 to 4), the thermoplastic elastomer composition of the present invention is excellent in all of mechanical strength, oil resistance, heat resistance and fuel oil resistance. I understand that.

Claims (9)

(A) a (meth) acrylic block copolymer, (B) a thermoplastic elastomer composition comprising a compound containing two or more amino groups in one molecule, (C) a thermoplastic resin and (D) a plasticizer. There,
The (meth) acrylic block copolymer (A) is composed of (A1) (meth) acrylic polymer block and (A2) acrylic polymer block, and in the main chain of at least one polymer block, Formula (1):

(Wherein R ¹ is hydrogen or a methyl group, two R ^{1 s} may be the same or different from each other, n is an integer of 0 to 3, and m is an integer of 0 or 1). Having at least one
A thermoplastic elastomer composition, wherein the (meth) acrylic block copolymer (A) is dynamically crosslinked in the thermoplastic resin (C) with the compound (B). (Meth) acrylic block copolymer (A) is a block copolymer represented by the general formula (A1-A2) _n , a block copolymer represented by the general formula A2- (A1-A2) _n , 2. The thermoplastic elastomer composition according to claim 1, which is at least one selected from the group consisting of a block copolymer represented by the general formula (A1-A2) _n -A1 (n is an integer of 1 or more). . The (meth) acrylic block copolymer (A) comprises (meth) acrylic polymer block (A1) 0.1 to 60% by weight and acrylic polymer block (A2) 99.9 to 40% by weight. The thermoplastic elastomer composition according to claim 1 or 2. The thermoplastic elastomer composition according to any one of claims 1 to 3, wherein the (meth) acrylic polymer block (A1) has an acid anhydride group. The thermoplastic elastomer composition according to any one of claims 1 to 3, wherein the acrylic polymer block (A2) has an acid anhydride group. The thermoplastic elastomer composition according to any one of claims 1 to 5, wherein the (meth) acrylic block copolymer (A) is obtained by controlled polymerization by atom transfer radical polymerization. The thermoplastic elastomer composition according to any one of claims 1 to 6, wherein the thermoplastic resin (C) is a polyamide-based resin and / or a polyester-based resin. The thermoplastic elastomer composition according to claim 7, wherein the thermoplastic resin (C) is a polyamide-based resin. The plasticizer (D) is at least one selected from the group consisting of a phthalic acid derivative, a hydroxybenzoic acid ester derivative, an N-alkylbenzenesulfonamide derivative, and an N-alkyltoluenesulfonamide derivative. The thermoplastic elastomer composition according to any one of the above.