JP2020056038A - Thermoplastic elastomer composition, foamed particle and foam-molded product - Google Patents

Abstract

To provide a thermoplastic elastomer composition capable of producing a foam-molded product having improved heat resistance.SOLUTION: The problem is solved by the thermoplastic elastomer composition including a thermoplastic elastomer and a pigment as a heat resistance improver for use in the production of a foam-molded product. In the thermoplastic elastomer composition, the thermoplastic elastomer exhibits crystallinity and is selected from an amide-based elastomer, an olefin-based elastomer, an ester-based elastomer and a urethane-based elastomer.SELECTED DRAWING: None

Description

  The present invention relates to a thermoplastic elastomer composition, foamed particles, and a foamed molded article. More particularly, the present invention relates to a colored foamed article having excellent heat resistance, a thermoplastic elastomer composition for producing the same, and foamed particles. The foam molded article of the present invention can be used in a wide variety of applications such as various building materials, shoe members (for example, insole members and midsole members), sporting goods, cushioning materials, seat cushions, and automobile members.

2. Description of the Related Art Conventionally, a polystyrene foam molded article using polystyrene as a base resin has been widely used as a cushioning material or a packing material. Here, the expanded molded article is obtained by expanding expandable particles such as expandable polystyrene particles by heating and expanding (pre-expanding) to obtain expanded particles (pre-expanded particles). , And then subjected to secondary foaming to integrate the foamed particles by thermal fusion.
It is known that a polystyrene foam molded article has high rigidity but low resilience because a monomer as a raw material is styrene. Therefore, there is a problem that it is difficult to use in applications where compression is repeated and applications where flexibility is required.
In order to improve the resilience of the foamed molded article, a foamed molded article using an amide-based elastomer, which is a kind of thermoplastic elastomer, as a base resin has been proposed (International Publication WO2016 / 052387: Patent Document 1). Amide-based elastomers have higher elasticity than polystyrene. Therefore, it is said that the resilience of a foam molded article using an amide-based elastomer as a base resin can be improved.

International Publication WO2016 / 052387

  In Patent Literature 1, a foam molded article having good resilience can be obtained. However, foamed molded articles are also required to have improved heat resistance in addition to resilience. In particular, since the thermoplastic elastomer has a hard segment and a soft segment, its heat resistance is lower than that of an existing thermoplastic resin. Therefore, provision of a foamed molded article made of a thermoplastic elastomer having improved heat resistance has been desired.

The inventors of the present invention have attempted to add various heat resistance improvers in order to improve the heat resistance of a foamed article made of a thermoplastic elastomer. As a result, it is surprising that the pigment can increase the crystallization temperature of the thermoplastic elastomer, and improve the heat resistance of the foam molded article produced from the thermoplastic elastomer composition containing the thermoplastic elastomer and the pigment. Have also led to the present invention.
Thus, according to the present invention, there is provided a thermoplastic elastomer composition comprising a thermoplastic elastomer and a pigment as a heat resistance improver.
Further, according to the present invention, there is provided foamed particles using a thermoplastic elastomer composition containing a thermoplastic elastomer and a pigment as a heat resistance improver as a base resin.
Further, according to the present invention, there is provided a foam molded article using a thermoplastic elastomer composition containing a thermoplastic elastomer and a pigment as a heat resistance improver as a base resin.

ADVANTAGE OF THE INVENTION According to this invention, the foam molding which has high heat resistance can be provided.
In any of the following cases, a foam molded article having higher heat resistance can be provided.
(1) The pigment is contained in an amount of 0.05 to 3.0 parts by mass based on 100 parts by mass of the thermoplastic elastomer.
(2) The thermoplastic elastomer exhibits crystallinity and is selected from amide elastomers, olefin elastomers, ester elastomers, and urethane elastomers.
(3) The thermoplastic elastomer is an amide-based elastomer, and the thermoplastic elastomer composition has a melting point higher by 20 to 30C than the crystallization temperature.
(4) The thermoplastic elastomer is an olefin-based elastomer, and the thermoplastic elastomer composition has a melting point higher by 30 to 45C than the crystallization temperature.
(5) The thermoplastic elastomer is an ester-based elastomer, and the thermoplastic elastomer composition has a melting point higher by 25 to 45 ° C. than the crystallization temperature.

It is explanatory drawing of the calculation method of solid viscoelasticity.

(Thermoplastic elastomer composition)
A thermoplastic elastomer composition (hereinafter, also simply referred to as a composition) includes a thermoplastic elastomer and a pigment. The composition is suitably used for producing expanded particles and expanded molded articles. The pigment plays a role as a heat resistance improver in the composition. Specifically, as confirmed in the examples, the pigment plays a role in increasing the crystallization temperature of the thermoplastic elastomer. By increasing the crystallization temperature, the crystallinity of the thermoplastic elastomer is increased, and as a result, the heat resistance of the foam molded article is improved. The inventors believe that the phenomenon that the heat resistance is improved by the pigment is not known in the technical field of using a thermoplastic elastomer for producing a foam molded article.

(1) Thermoplastic elastomer The thermoplastic elastomer can be selected from, for example, an amide-based elastomer, an olefin-based elastomer, an ester-based elastomer, and a urethane-based elastomer. The composition may include only various elastomers, or may include a mixture of each elastomer. The thermoplastic elastomer preferably has crystallinity. The presence or absence of crystallinity can be determined by the presence or absence of a crystallization temperature.
(I) Amide-based elastomer The amide-based elastomer may be crosslinked or non-crosslinked. In the present specification, the term "non-crosslinked" means a foamed particle having an insoluble gel fraction of 3.0% by mass or less in an alcohol solvent. Crosslinking means that the gel fraction is more than 3.0% by mass.

Here, the gel fraction of the amide-based elastomer (foam) is measured in the following manner.
The mass W1 of the foam is measured. Next, the foam is immersed in 100 mL of an alcohol-based solvent (eg, 3-methoxy-3-methyl-1-butanol) at 130 ° C. for 24 hours.
Next, the residue of the alcohol-based solvent was filtered using an 80-mesh wire gauze, the residue remaining on the wire gauze was dried at 130 ° C. for 1 hour, and the mass W2 of the residue remaining on the wire gauze was measured. Then, the gel fraction of the foam can be calculated based on the following equation.
Gel fraction (% by mass) = W2 / W1 × 100
The base resin preferably contains a non-crosslinked amide elastomer.

As the non-crosslinked amide elastomer, a copolymer having a polyamide block (hard segment) and a polyether block (soft segment) can be used.
Examples of the polyamide block include polyε coupleramide (nylon 6), polytetramethylene adipamide (nylon 46), polyhexamethylene adipamide (nylon 66), polyhexamethylene sebacamide (nylon 610), and polyhexamethylene sebacamide (nylon 610). Methylene dodecamide (nylon 612), polyundecamethylene adipamide (nylon 116), polyundecaneamide (nylon 11), polylauramide (nylon 12), polyhexamethylene isophthalamide (nylon 6I), polyhexamethylene terephthalamide ( Polyamide structures such as nylon 6T), polynanomethylene terephthalamide (nylon 9T), and polymethaxylylene adipamide (nylon MXD6). The polyamide block may be a combination of units constituting these polyamide structures.
Examples of the polyether block include polyether structures such as polyethylene glycol (PEG), polypropylene glycol (PPG), polytetramethylene glycol (PTMG), and polytetrahydrofuran (PTHF). The polyether block may be a combination of units constituting these polyether structures.
The polyamide block and the polyether block may be randomly dispersed.

The number average molecular weight of the polyamide block is preferably from 300 to 15,000, more preferably from 600 to 5,000. The number average molecular weight Mn of the polyether block is preferably from 100 to 6000, and more preferably from 200 to 3,000.
Non-crosslinked amide elastomers include U.S. Pat.No. 4,331,786, U.S. Pat.No. 4,115,475, U.S. Pat.No. 4,195,015, U.S. Pat.No.4,839,441, U.S. Pat. Amide-based elastomers described in US Pat. No. 4,230,838 and US Pat. No. 4,332,920 can also be used.

The non-crosslinked amide-based elastomer is preferably one obtained by copolycondensation of a polyamide block having a reactive terminal and a polyether block having a reactive terminal. The copolycondensation may include, in particular:
(A) copolycondensation of a polyamide block having a diamine chain end and a polyoxyalkylene block having a dicarboxylic acid chain end,
(B) a mixture of a polyamide unit having a dicarboxylic acid chain end and a polyoxyalkylene unit having a diamine chain end obtained by cyanoethylation and hydrogenation of an aliphatic dihydroxylated α, ω-polyoxyalkylene unit called polyether diol; Copolycondensation,
(C) Copolycondensation of a polyamide unit having a dicarboxylic acid chain end with a polyether diol (the one obtained in this case is particularly called polyetheresteramide).

Examples of the compound that provides a polyamide block having a dicarboxylic acid chain end include a compound obtained by condensation of a dicarboxylic acid and a diamine in the presence of a chain regulator of α, ω-aminocarboxylic acid, lactam or dicarboxylic acid. .
In the case of the copolycondensation of (a), the non-crosslinked amide-based elastomer is prepared, for example, by mixing a polyether diol, a lactam (or an α, ω-amino acid) and a diacid as a chain stopper in the presence of a small amount of water. It can be obtained by reacting. The non-crosslinked amide-based elastomer may have polyether blocks and polyamide blocks of various lengths, and may be dispersed in the polymer chain by reacting each component at random.

  In the above copolycondensation, the block of polyether diol may be used as it is, or its hydroxyl group and a polyamide block having a carboxy terminal group may be copolymerized and used, and the hydroxyl group is aminated to form polyether diamine. After the conversion, it may be used by condensation with a polyamide block having a carboxy terminal group. In addition, a polymer containing a polyamide block and a polyether block dispersed at random can be obtained by mixing and copolycondensing a block of polyether diol with a polyamide precursor and a chain limiting agent.

(Ii) Olefin-based elastomer The olefin-based elastomer may be crosslinked or non-crosslinked. Non-crosslinked means a foam having a gel fraction insoluble in xylene of 3.0% by mass or less. Crosslinking means that the gel fraction is more than 3.0% by mass.
Here, the gel fraction of the olefin elastomer (foam) is measured in the following manner.
The mass W1 of the foam is measured. The foam is then heated at reflux for 3 hours in 80 ml of boiling xylene. Next, the residue in xylene was filtered using an 80 mesh wire mesh, the residue remaining on the wire mesh was dried at 130 ° C. for 1 hour, and the mass W2 of the residue remaining on the wire mesh was measured. The gel fraction of the foam can be calculated based on the following equation.
Gel fraction (% by mass) = W2 / W1 × 100
It is preferable that the base resin contains a non-crosslinked olefin elastomer.
It is preferable that the non-crosslinked olefin-based elastomer be capable of imparting a predetermined density and a permanent compression set to the foam without containing mineral oil. Examples of the non-crosslinked olefin-based elastomer include those having a structure in which a hard segment and a soft segment are combined. Such a structure gives rubber elasticity at normal temperature and is plasticized and moldable at high temperature.
For example, a non-crosslinked olefin-based elastomer in which the hard segment is a polypropylene-based resin and the soft segment is a polyethylene-based resin is exemplified.

As the former polypropylene-based resin, a resin containing polypropylene as a main component can be used. The polypropylene may have a stereoregularity selected from isotactic, syndiotactic, atactic and the like.
As the latter polyethylene resin, a resin containing polyethylene as a main component can be used. Components other than polyethylene include polyolefins such as polypropylene and polybutene.

The non-crosslinked olefin-based elastomer may contain a softener such as a lubricating oil, paraffin, coconut oil, stearic acid, or fatty acid.
As the non-crosslinked olefin-based elastomer, a polymerization type elastomer produced by polymerizing a monomer serving as a hard segment and a monomer serving as a soft segment and directly producing the same in a polymerization reaction vessel; a kneading machine such as a Banbury mixer or a twin screw extruder; And a blend-type elastomer produced by physically dispersing a polypropylene resin serving as a hard segment and a polyethylene resin serving as a soft segment using the above.

The non-crosslinked olefin elastomer preferably has a Shore A hardness of 30 to 100, and more preferably 40 to 90. The hardness of the non-crosslinked olefin-based elastomer is measured according to a durometer hardness test (JIS K6253: 97).
The non-crosslinked olefin-based elastomer preferably has a Shore D hardness of 10 to 70, and more preferably 20 to 60. The hardness of the non-crosslinked olefin elastomer is measured according to a durometer hardness test (ASTM D2240: 95).

(Iii) Ester-based elastomer Examples of the ester-based elastomer include an ester-based elastomer containing a hard segment and a soft segment.
The hard segment is composed of, for example, a dicarboxylic acid component and / or a diol component. It may be composed of two components, a dicarboxylic acid component, and a dicarboxylic acid component and a diol component.
Examples of the dicarboxylic acid component include components derived from aliphatic dicarboxylic acids such as oxalic acid, malonic acid, and succinic acid, and derivatives thereof, and aromatic dicarboxylic acids such as terephthalic acid, isophthalic acid, and naphthalenedicarboxylic acid, and derivatives thereof.
Examples of the diol component include _C2-10 alkylene glycols such as ethylene glycol, propylene glycol, and butanediol (for example, 1,4-butanediol), (poly) oxy _C2-10 alkylene glycol, and _C5-12 cycloalkanediol. , Bisphenols or their alkylene oxide adducts. The hard segment may have crystallinity.

As the soft segment, a polyester type and / or polyether type segment can be used.
Polyester type soft segments include dicarboxylic acids (aliphatic C _4-12 dicarboxylic acids such as adipic acid) and diols (C _2-10 alkylene glycols such as 1,4-butanediol and ethylene glycols). Aliphatic polyesters such as polycondensates with (poly) oxy C _2-10 alkylene glycol), polycondensates of oxycarboxylic acid and ring-opening polymers of lactones (C _3-12 lactones such as ε-caprolactone) Is mentioned. The polyester type soft segment may be amorphous. Specific examples of the polyester as a soft segment, caprolactone polymers, polyethylene adipate, polyesters of C _2-6 alkylene glycol and C _6-12 alkane dicarboxylic acids such as polybutylene adipate. The number average molecular weight of this polyester may be in the range of 200 to 15,000, may be in the range of 200 to 10000, and may be in the range of 300 to 8000.
Examples of the polyether type soft segment include a segment derived from an aliphatic polyether such as polyalkylene glycol (for example, polyoxyethylene glycol, polyoxypropylene glycol, polyoxytetramethylene glycol).
The number average molecular weight of the polyether may be in the range of 200 to 10000, may be in the range of 200 to 6000, and may be in the range of 300 to 5000.

The soft segment includes a polyester having a polyether unit such as a copolymer of an aliphatic polyester and a polyether (polyether-polyester), and a polyether such as a polyoxyalkylene glycol (for example, polyoxytetramethylene glycol). And a segment derived from a polyester of an aliphatic dicarboxylic acid.
The mass ratio between the hard segment and the soft segment may be from 20:80 to 90:10, may be from 30:70 to 90:10, may be from 30:70 to 80:20, The ratio may be 40:60 to 80:20, or may be 40:60 to 75:25.
When the dicarboxylic acid component is a terephthalic acid component and a dicarboxylic acid component other than the terephthalic acid component, the ester elastomer contains 30 to 80% by mass of a hard segment and contains 5% of a dicarboxylic acid component other than the terephthalic acid component. -30% by mass. The proportion of the dicarboxylic acid component other than the terephthalic acid component may be 5 to 25% by mass, 5 to 20% by mass, or 10 to 20% by mass. The ratio of the dicarboxylic acid component can be obtained by quantitatively evaluating the NMR spectrum of the resin.
Preferably, the dicarboxylic acid component other than the terephthalic acid component is an isophthalic acid component. By containing the isophthalic acid component, the crystallinity of the elastomer tends to decrease, and the foam moldability is improved, so that a foam molded article having a lower density can be obtained.
As the ester-based elastomer, a PELPrene series and a VYLON series manufactured by Toyobo can be preferably used. In particular, it is preferable to use the perprene series.

(Iv) Urethane-based elastomer As the polyurethane-based elastomer, for example, an elastomer obtained from a long-chain polyol, short-chain glycol, diisocyanate or the like as a raw material via a urethane bond in a molecule by a polyaddition reaction can be used. Examples of the chain polyol include poly (ethylene adipate), poly (diethylene adipate), poly (1,4-butylene adipate), poly (1,6-hexane adipate), polylactone diol, polycaprolactone diol, and polyenanthractone diol. , Polyethylene glycol, polypropylene glycol, polytetramethylene glycol, poly (propylene glycol / ethylene glycol), poly (1,6-hexamethylene glycol carbonate) and the like. The molecular weight of the long-chain polyol may be 100 to 10000, or may be 500 to 5000.

As the short-chain glycol, ethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 2,3-butanediol , 2,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,4-xylylene glycol, bisphenol A, hydroquinone diethylol ether, phenylene bis- (β-hydroxyethyl ether) and the like. No.
Examples of the diisocyanate include 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, phenylene diisocyanate, 4,4′-diphenylmethane diisocyanate, 4,4′-diphenyl diisocyanate, , 5-Naphthalene diisocyanate, 3,3'-dimethylbiphenyl-4,4'-diisocyanate, o-xylene diisocyanate, m-xylene diisocyanate, p-xylene diisocyanate, tetramethylene diisocyanate Examples thereof include nate, hexamethylene diisocyanate, trimethylhexamethylene diisocyanate, dodecamethylene diisocyanate, cyclohexane diisocyanate, dicyclohexylmethane diisocyanate, and isophorone diisocyanate.

A soft segment may be constituted by a polyurethane elastomer, a long-chain polyol and a diisocyanate, and a hard segment may be constituted by a short-chain glycol and a diisocyanate.
Polyurethane-based elastomers may be modified, if necessary, by maleation, carboxylation, hydroxylation, epoxidation, halogenation, sulfonation, etc., sulfur crosslinking, peroxide crosslinking, metal ion crosslinking, electron beam crosslinking, silane crosslinking, etc. It may be subjected to a crosslinking treatment such as crosslinking.
The polyurethane elastomer may have a viscosity molecular weight of 5,000 to 300,000 and 10,000 to 100,000 from the viewpoint of toughness and flexibility as a molded article.
The polyurethane-based elastomer may have a number average molecular weight of 3,000 to 200,000, 5,000 to 180,000, 8,000 to 150,000.

(2) Pigment The pigment used as the heat resistance improver is not particularly limited as long as the heat resistance of the foamed molded article can be improved. Here, the pigment may have a function of increasing the crystallization temperature of the composition by 10 ° C. or more than the crystallization temperature of the thermoplastic elastomer. The pigment also has a normal coloring function as a pigment. Therefore, it is possible to color the foamed particles and the foamed molded article into a desired color.
Examples of pigments include carbon, titanium oxide, iron oxide, iron hydroxide, chromium oxide, spinel, lead chromate, vermilion chromate, navy blue, aluminum powder, bronze powder, and carbonic acid. Calcium, barium sulfate, silicon oxide, aluminum hydroxide, phthalocyanine, azo, condensed azo, anthraquinone, azine, quinoline, quinacdrine, perinone / perylene, indigo / thioindico, iso Pigments of indolinone type, azomethine azo type, dioxazine type, quinacridone type, aniline black type, triphenylmethane type and the like can be mentioned. The pigments may be used alone or as a mixture of two or more.

Examples of the carbon-based pigment include carbon black, channel black, furnace black, acetylene black, anthracene black, oil smoke, pine smoke, and graphite.
Other pigments include
Copper phthalocyanine, isoindoline, dichloroquinacridone, diketopyrrolopyrrole,
C. I. Pigment Red 2, C.I. I. Pigment Red 3, C.I. I. Pigment Red 5, C.I. I. Pigment Red 17, C.I. I. Pigment Red 22, C.I. I. Pigment Red 38, C.I. I. Pigment Red 41, C.I. I. Pigment Red 48: 1, C.I. I. Pigment Red 48: 2, C.I. I. Pigment Red 48: 3, C.I. I. Pigment Red 48: 4, C.I. I. Pigment Red 49, C.I. I. Pigment Red 50: 1, C.I. I. Pigment Red 53: 1, C.I. I. Pigment Red 57: 1, C.I. I. Pigment Red 58: 2, C.I. I. Pigment Red 60, C.I. I. Pigment Red 63: 1, C.I. I. Pigment Red 63: 2, C.I. I. Pigment Red 64: 1, C.I. I. Pigment Red 88, C.I. I. Pigment Red 112, C.I. I. Pigment Red 122, C.I. I. Pigment Red 123, C.I. I. Pigment red 144, C.I.
I. Pigment Red 146, C.I. I. Pigment Red 149, C.I. I. Pigment Red 166, C.I. I. Pigment Red 168, C.I. I. Pigment Red 170, C.I. I. Pigment red 176, C.I. I. Pigment Red 177, C.I. I. Pigment Red 178, C.I. I. Pigment Red 179, C.I. I. Pigment Red 180, C.I. I. Pigment Red 185, C.I. I. Pigment Red 190, C.I. I. Pigment Red 194, C.I. I. Pigment Red 202, C.I. I. Pigment Red 206, C.I. I. Pigment Red 207, C.I. I. Pigment Red 209, C.I. I. Pigment Red 216, C.I. I. Pigment Red 245, C.I. I. Pigment Violet 19,

C. I. Pigment Blue 2, C.I. I. Pigment Blue 15, C.I. I. Pigment Blue 15: 1, C.I. I. Pigment Blue 15: 2, C.I. I. Pigment Blue 15: 3, C.I. I. Pigment Blue 15: 4, C.I. I. Pigment Blue 15: 5, C.I. I. Pigment Blue 16, C.I. I. Pigment Blue 17, C.I. I. Pigment Blue 22, C.I. I. Pigment Blue 25, C.I. I. Pigment Blue 28, C.I. I. Pigment Blue 60, C.I. I. Pigment Blue 66,
C. I. Pigment Green 7, C.I. I. Pigment Green 10, C.I. I. Pigment Green 26, C.I. I. Pigment Green 36, C.I. I. Pigment Green 50,
C. I. Pigment Yellow 1, C.I. I. Pigment Yellow 3, C.I. I. Pigment Yellow 11, C.I. I. Pigment Yellow 12, C.I. I. Pigment Yellow 13, C.I. I. Pigment Yellow 14, C.I. I. Pigment Yellow 17, C.I. I. Pigment Yellow 21, C.I. I. Pigment Yellow 35, C.I. I. Pigment yellow 53, C.I. I. Pigment yellow 55, C.I. I. Pigment yellow 74, C.I. I. Pigment yellow 76, C.I. I. Pigment yellow 82, C.I. I. Pigment yellow 83, C.I. I. Pigment Yellow 102, C.I. I. Pigment yellow 110, C.I. I. Pigment Yellow 128, C.I. I. Pigment yellow 153, C.I. I. Pigment yellow 157, C.I. I. Pigment Yellow 161, C.I. I. Pigment yellow 167, C.I. I. Pigment Yellow 173, C.I. I. Pigment Yellow 184
And the like.

(3) Content Ratio of Thermoplastic Elastomer and Pigment The pigment is preferably contained in an amount of 0.05 to 3.0 parts by mass based on 100 parts by mass of the thermoplastic elastomer. If the amount is less than 0.05 parts by mass, the effect of improving heat resistance may not be sufficient. If the amount is more than 3.0 parts by mass, foaming may be hindered. The content ratio of the pigment is more preferably 0.1 to 2.0 parts by mass, and further preferably 0.2 to 1.0 parts by mass.

(4) Additives In the base resin, additives, amide resins (excluding elastomers), olefin resins (excluding elastomers), and ester resins (excluding elastomers) as long as the effects of the present invention are not impaired. ), Urethane-based resins (excluding elastomers), and other resins such as polyether resins. The other resin may be a known thermoplastic resin or thermosetting resin.

(5) Crystallization Temperature and Melting Point of the Composition When the thermoplastic elastomer is an amide-based elastomer, the composition preferably has a melting point higher by 20 to 30 ° C. than the crystallization temperature.
When the thermoplastic elastomer is an olefin-based elastomer, the composition preferably has a melting point higher by 30 to 45C than the crystallization temperature.
When the thermoplastic elastomer is an ester-based elastomer, the composition preferably has a melting point higher by 25 to 45C than the crystallization temperature.
When the composition has the above-mentioned relationship between the crystallization temperature and the melting point, it is possible to provide a composition capable of producing a foam molded article having higher heat resistance.
The melting point of the composition is
For amide elastomers, 20 to 25 ° C. higher than the crystallization temperature,
For olefin-based elastomers, 30 to 35 ° C. higher than the crystallization temperature,
As for the ester-based elastomer, it is more preferable that the temperature is higher by 25 to 35 ° C. than the crystallization temperature.

(Expanded particles)
The expanded particles use a thermoplastic elastomer composition containing a thermoplastic elastomer and a pigment as a heat resistance improver as a base resin. The expanded particles have high heat resistance by containing the pigment.
The thermoplastic elastomer, the pigment and the content ratio of the expanded particles are the same as those of the thermoplastic elastomer composition.
Foamed particles preferably have a bulk density of 0.05 to 0.5 g / cm ^3. The bulk density is more preferably 0.10 to 0.25 g / cm ³ .
The expanded particles preferably have an open cell ratio of 10% or less. The open cell ratio is more preferably 5% or less. The lower limit is 0%.
The expanded particles preferably have an average particle diameter of 1 to 10 mm. The average particle size is more preferably 2 to 5 mm.
The expanded particles can be obtained through a step of impregnating the resin particles with a blowing agent to obtain expandable particles (impregnation step) and an expansion step of expanding the expandable particles.

(1) Impregnation Step (a) Resin Particles Resin particles can be obtained using a known production method and production equipment.
For example, resin particles can be produced by granulating a melt-kneaded product of a resin and a pigment extruded from an extruder by underwater cutting, strand cutting, or the like. The temperature, time, pressure, etc., during melt-kneading can be appropriately set according to the raw materials used and the production equipment.
The melt-kneading temperature in the extruder at the time of melt-kneading is a temperature at which the resin is sufficiently softened, preferably from 170 to 250C, more preferably from 200 to 230C. The melt-kneading temperature means the temperature of the melt-kneaded material inside the extruder obtained by measuring the temperature at the center of the flow path of the melt-kneaded material near the extruder head with a thermocouple thermometer.
The pigment may be fed to the extruder in the form of a masterbatch. Examples of the resin component constituting the master batch include thermoplastic elastomer resins such as polyolefin resins such as polyethylene and polypropylene, amide elastomers, ester elastomers, olefin elastomers, and urethane elastomers. Among them, a thermoplastic elastomer resin is preferable.
The shape of the resin particles is, for example, a true sphere, an oval sphere (egg), a column, a prism, a pellet, or a granular shape.
The resin particles preferably have an average particle size of 0.5 to 3.5 mm. If the average particle diameter is less than 0.5 mm, the holding power of the blowing agent may be reduced, and the foaming property may be reduced. If it is larger than 3.5 mm, the filling property into the mold may decrease.
The resin particles preferably have an L / D of 0.5 to 3 when the length is L and the average diameter is D. When the L / D of the resin particles is less than 0.5 or more than 3, the filling property in the mold may be reduced. The length L of the resin particles refers to the length in the extrusion direction, and the average diameter D refers to the diameter of the cut surface of the resin particles substantially orthogonal to the direction of the length L.
The average diameter D of the resin particles is preferably 0.5 to 3.5 mm. When the average diameter is less than 0.5 mm, the retention of the foaming agent may be reduced, and the foamability of the expandable particles may be reduced. If it is larger than 3.5 mm, the filling property of the foamed particles into the mold is reduced, and the thickness of the foam may not be reduced when a plate-like foam is produced.

The resin particles may contain a cell regulator.
Examples of the cell regulator include citric acid sodium bicarbonate, higher fatty acid amide, higher fatty acid bisamide, higher fatty acid salt, and inorganic cell nucleating agent. These air conditioners may be used in combination of two or more.
Examples of the higher fatty acid amide include stearic acid amide and 12-hydroxystearic acid amide.
Examples of the higher fatty acid bisamide include ethylene bisstearic acid amide, ethylene bis-12-hydroxystearic acid amide, and methylene bisstearic acid amide.
Examples of higher fatty acid salts include calcium stearate.
Examples of the inorganic cell nucleating agent include talc, calcium silicate, and synthetic or naturally produced silicon dioxide.
The resin particles may further contain a flame retardant such as hexabromocyclododecane and triallyl isocyanurate hexabromide.

(B) Expandable particles Expandable particles are produced by impregnating resin particles with a blowing agent. A known procedure can be used as a procedure for impregnating the resin particles with the foaming agent. For example, in a sealable autoclave, by supplying and stirring the resin particles, dispersant and water, the resin particles are dispersed in water to produce a dispersion, and a foaming agent is pressed into the dispersion, A method of impregnating resin particles with a foaming agent (wet impregnation) may be mentioned. The foaming agent may be impregnated without using water (dry impregnation).
The dispersant is not particularly limited, and examples thereof include poorly water-soluble inorganic substances such as calcium phosphate, magnesium pyrophosphate, sodium pyrophosphate, magnesium oxide, and hydroxyapatite, and surfactants such as sodium dodecylbenzenesulfonate.
As the foaming agent, general-purpose ones are used, and examples thereof include inorganic gases such as air, nitrogen, and carbon dioxide (carbon dioxide); aliphatic hydrocarbons such as propane, butane, and pentane; and halogenated hydrocarbons. Group hydrocarbons and inorganic gases are preferred. The blowing agents may be used alone or in combination of two or more.

  The amount of the foaming agent to be impregnated into the resin particles is preferably 1 to 12 parts by mass with respect to 100 parts by mass of the resin particles. When the content of the foaming agent is less than 1 part by mass, the foaming power is reduced, and it may be difficult to favorably foam at a high foaming ratio. If the amount exceeds 12 parts by mass, the cell membrane is easily broken, the plasticizing effect becomes too large, the viscosity at the time of foaming tends to decrease, and shrinkage tends to occur. When an aliphatic hydrocarbon is used as the blowing agent, a more preferable amount of the blowing agent is 6 to 8 parts by mass. Within this range, the foaming power can be sufficiently increased, and even if the foaming ratio is high, foaming can be performed more favorably. When the content of the foaming agent is 8 parts by mass or less, breakage of the cell membrane is suppressed, and the plasticizing effect is not excessively increased. .

The content (impregnation amount) of the foaming agent impregnated with respect to 100 parts by mass of the resin particles is measured as follows.
The mass Xg before the resin particles are placed in the pressure vessel is measured. After impregnating the resin particles with the foaming agent in the pressure vessel, the mass Yg after removing the impregnated material from the pressure vessel is measured. The content (impregnation amount) of the foaming agent impregnated with respect to 100 parts by mass of the resin particles is determined by the following formula.
Content of foaming agent (parts by mass) = ((Y−X) / X) × 100
When an aliphatic hydrocarbon is used as the foaming agent, if the impregnation temperature of the resin particles with the foaming agent is low, the time required for impregnating the resin particles with the foaming agent becomes long, and the production efficiency may decrease. On the other hand, if it is too high, the resin particles may fuse together to form bonded particles. The impregnation temperature is
Room temperature (25 ° C) to 120 ° C is preferable, and 50 to 110 ° C is more preferable. A foaming aid (plasticizer) may be used in combination with a foaming agent. Examples of the foaming auxiliary (plasticizer) include diisobutyl adipate, toluene, cyclohexane, ethylbenzene and the like.

(2) Foaming Step In the foaming step, the foaming temperature and the heating medium are not particularly limited as long as foamable particles can be obtained by foaming the expandable particles.
Before foaming, an anti-coalescing agent such as polyamide powder or a surfactant, or an antistatic agent may be applied to the surface of the expandable particles. Examples of the antistatic agent include polyoxyethylene alkylphenol ether and stearic acid monoglyceride.

(Foam molding)
The foamed molded article uses, as a base resin, a thermoplastic elastomer composition containing a thermoplastic elastomer and a pigment as a heat resistance improver. The foam molded article has high heat resistance by containing a pigment. Further, the foamed molded body is formed of a fusion body of a plurality of foamed particles.
The thermoplastic elastomer, the pigment and the content ratio thereof in the foam molded article are the same as those of the thermoplastic elastomer composition.
The foam molded article preferably has a density of 0.05 to 0.25 g / cm ³ . The density is more preferably 0.10 to 0.20 g / cm ³ .
The foam molded article can be used in a wide range of applications such as various building materials, shoe members (for example, insole members and midsole members), sporting goods, cushioning materials, seat cushions, and automobile members.
The foamed molded article can be manufactured by heating and molding a pair of molds in which a plurality of foamed particles are filled in a mold with a heating medium. For example, filling the foamed particles into a mold constituted by a mold having a large number of small holes, heating and foaming the foamed particles with pressurized steam, filling the gaps between the foamed particles, and fusing the foamed particles to each other. Can be obtained by integrating them.

The foaming particles may be impregnated with an inert gas or air (hereinafter, referred to as an inert gas or the like) to improve the foaming power of the foaming particles. By improving the foaming power, the fusion property between the foamed particles during heating and foaming is improved, and the foam has more excellent foamability. Note that examples of the inert gas include carbon dioxide, nitrogen, helium, and argon.
As a method of impregnating the foamed particles with an inert gas or the like, for example, a method of impregnating the foamed particles with an inert gas or the like by placing the foamed particles in an atmosphere of an inert gas or the like having a pressure equal to or higher than normal pressure Is mentioned. The foamed particles may be impregnated with an inert gas or the like before filling in the mold, but are impregnated by placing the foamed particles in the mold and then placing the mold under an atmosphere of an inert gas or the like. You may. When the inert gas is nitrogen, it is preferable to leave the foamed particles in a nitrogen atmosphere of 0.1 to 2.0 MPa (gauge pressure) for 20 minutes to 24 hours.

Next, the present invention will be described in more detail by way of examples, but the present invention is not limited thereto.
<Melting point and crystallization temperature of elastomer and composition>
It conformed to JIS K7121: 1987, 2012 “Method of measuring transition temperature of plastic” and JIS K7122: 1987, 2012 “Method of measuring transition heat of plastic”. However, the sampling method and temperature conditions were as follows. Using a differential scanning calorimeter "DSC6220, ASD-2" manufactured by SII Nanotechnology Co., Ltd. or a differential scanning calorimeter "DSC7000X, AS-3" manufactured by Hitachi High-Tech Science Co., Ltd. so that there is no gap between the bottom of the aluminum measuring container. , And the temperature was lowered from 30 ° C. to −70 ° C. under a nitrogen gas flow rate of 20 mL / min, held for 10 minutes, and then raised from −70 ° C. to 220 ° C. (1st Heating), and held for 10 minutes. A DSC curve was obtained when the temperature was lowered from 220 ° C. to −70 ° C. (Cooling), and after holding for 10 minutes, the temperature was raised from −70 ° C. to 220 ° C. (2nd Heating). In addition, all the temperature raising / lowering was performed at a rate of 10 ° C./min, and alumina was used as a reference substance. In the present invention, the melting point is a value obtained by reading the temperature at the top of the largest melting peak observed in the second heating process using analysis software attached to the apparatus. The crystallization temperature was a value obtained by reading the top temperature of the crystallization peak on the highest temperature side having a calorie of 3 mJ / mg or more, which was observed in the cooling process, using analysis software attached to the apparatus.

<Length L and average diameter D of resin particles>
The length L and the average diameter D of the resin particles were measured using calipers. The length in the extrusion direction when producing the resin particles was L, and the length in the direction perpendicular to the extrusion direction was the average diameter D.

<Bulk density of expanded particles>
First, Wg was collected as a measurement sample of foamed particles, and the measurement sample was dropped naturally into a measuring cylinder. Then, the apparent volume (V) cm ³ of the sample was fixed by hitting the bottom of the measuring cylinder, and the mass and the mass were measured. The volume was measured, and the bulk density of the expanded particles was calculated based on the following equation.
Bulk density (g / cm ³ ) = mass of measurement sample (W) / volume of measurement sample (V)

<Average particle diameter of expanded particles>
Approximately 50 g of the foamed particles were sieved using a low tap sieve shaker (manufactured by Iida Seisakusho Co., Ltd.) to 16.00 mm, 13.20 mm, 11.20 mm, 9.50 mm, 8.00 mm, 6.70 mm, and 5. Classified with a 60 mm, 4.75 mm, 4.00 mm, 3.35 mm, 2.80 mm, 2.36 mm, 2.00 mm, 1.70 mm, 1.40 mm, 1.18 mm, and 1.00 mm JIS standard sieve for 5 minutes. . The sample mass on the sieve net was measured, and the particle size (median size) at which the cumulative mass became 50% was defined as the average particle size based on the cumulative mass distribution curve obtained from the result.

<Open cell ratio of expanded particles>
First, a sample cup of a volume measurement air comparison hydrometer was prepared, and the total mass A (g) of the foamed particles in an amount satisfying about 80% of the sample cup was measured. Next, the volume B (cm ³ ) of the whole expanded particles was measured by a 1-1 / 2-1 atmospheric pressure method using a hydrometer. The specific gravity meter used was, for example, a product marketed under the trade name “1000 type” by Tokyo Science Corporation. Subsequently, a wire mesh container was prepared, the wire mesh container was immersed in water, and the mass C (g) of the wire mesh container in the state of being immersed in the water was measured. Next, after putting all of the foamed particles in the wire mesh container, the wire mesh container is immersed in water, and the wire mesh container in the state of being immersed in water and the foaming material placed in the wire mesh container are immersed in water. The mass D (g) including the total amount of the particles was measured. Then, the apparent volume E (cm ³ ) of the expanded particles is calculated based on the following equation, and the open cell ratio of the expanded particles is calculated by the following equation based on the apparent volume E and the volume B (cm ³ ) of the entire expanded particle. Was calculated. In calculating the open cell ratio, the volume of 1 g of water was set to 1 cm ³ .
E = A + (CD)
Open cell ratio (%) = 100 × (EB) / E

<The density of the foamed molded article>
The density of the foamed molded article was measured by the method described in JIS K7222: 2005 "Foamed plastic and rubber-Determination of apparent density". That is, a test piece of 100 cm ³ or more was cut without changing the original cell structure of the material, and the mass was measured and calculated by the following equation.
Density (g / cm ³ ) = test piece mass (g) / test piece volume (cm ³ )
A test piece for measurement was cut into a 100 mm × 100 mm × original molded article thickness from a sample 72 hours or more after molding, and was subjected to a temperature of 23 ± 2 ° C. and a humidity of 50 ± 5% or a temperature of 27 ± 2 ° C. and a humidity of 65 ±. What was left for more than 16 hours in an atmosphere condition of 5% was used.

<Solid viscoelasticity of foam molding>
As a solid viscoelasticity measuring device, a viscoelastic spectrometer EXSTAR DMS6100 (manufactured by SII Nanotechnology Inc.) was used. First, the molded foam was dried in an oven at 100 ° C. for 3 hours. Thereafter, pressing was performed at 200 ° C. for 5 minutes using a hot press machine to obtain a measurement sample having a length of 40 mm, a width of 10 mm and a thickness of 0.7 mm. Using a solid viscoelasticity measuring device, in a tension control mode, under a nitrogen atmosphere, a frequency of 1 Hz, a heating rate of 5 ° C./min, a measuring temperature of 30 ° C. to 220 ° C., a chuck interval of 20 mm, a strain amplitude of 5 μm, and a minimum tension / compression force of 20 mN. The solid viscoelasticity was measured under the conditions of a tension / compression force gain of 1.2 and a force amplitude initial value of 20 mN. The value of the temperature indicated by the intersection of the tangent to the inflection point in the solid viscoelasticity graph obtained from the measurement was calculated. FIG. 1 shows an example of how to draw tangents.

Example 1
(1) Resin particles Amide-based elastomer having nylon 12 as a hard segment and polytetramethylene glycol as a soft segment (trade name “PEBAX5533”, melting point 160.1 ° C., crystallization temperature 124.5 ° C., manufactured by Arkema) 100 Parts by mass, 2.0 parts by mass of a carbon black amide-based elastomer resin masterbatch (resin constituting: "PEBAX5533", pigment concentration 10% by mass, manufactured by Saika Chemical Co., Ltd.) as an pigment, and an organic foam modifier ( An amide-based elastomer composition was obtained by supplying 0.3 parts by mass (trade name “Kao Wax EBFF”, manufactured by Kao Corporation) to a single screw extruder and melt-kneading. In the single screw extruder, the composition was initially melt-kneaded at 180 ° C. and then melt-kneaded while increasing the temperature to 220 ° C.
Then, after cooling the composition in the molten state, the amide-based elastomer was extruded from each nozzle of the multi-nozzle mold attached to the front end of the single screw extruder. In addition, the resin was extruded from each nozzle of a multi-nozzle mold (having eight nozzles having a diameter of 1.3 mm) attached to the front end of the single screw extruder, and cut in water at 30 to 50 ° C. The obtained resin particles had a particle length L of 1.0 to 1.4 mm and an average particle diameter D of 1.0 to 1.4 mm. The melting point of the resin particles (composition) was 160.5 ° C and the crystallization temperature was 136.3 ° C.

(2) Expandable Particles 15 kg (100 parts by mass) of resin particles (average particle diameter 1.2 mm) were put into a 43 liter internal pressure-resistant rotary mixer capable of being heated and sealed. Further, 0.5 parts by mass of Epan 450 (manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) was added as a coalescence inhibitor and stirred. While stirring the resin particles, 12 parts by mass of butane (normal butane: isobutane = 7: 3) was injected as a foaming agent, the internal temperature was increased to 70 ° C., and stirring was continued for 2 hours. Immediately after the pressure was released from the mixer, the foamable particles were obtained.
(3) Expanded Particles 2 kg of expandable particles are charged into a cylindrical prefoaming machine having an inner volume of 50 L with a stirrer, and foamed while stirring with steam of 0.21 MPa to form expanded particles having a bulk density of 0.09 g / cm ³ . I got The obtained foamed particles were put in a closed container, and nitrogen was injected into the closed container at a pressure of 0.5 MPa and allowed to stand at room temperature for 18 hours to impregnate the foamed particles with nitrogen.
(4) Foamed molded article The foamed particles are taken out of the closed container, filled in a cavity of a mold having a cavity having a size of 400 mm x 300 mm x thickness of 11.0 mm, and heated with steam of 0.25 MPa for 35 seconds for molding. Then, a foam molded article was obtained.
The density of the foam molded article was 0.10 g / cm ³ , and the solid viscoelasticity was 152.3 ° C.

Example 2
The pigment is a copper phthalocyanine amide-based elastomer resin masterbatch (constituting resin:
A foam molded article was obtained in the same manner as in Example 1 except that “PEBAX5533”, a pigment concentration of 10% by mass, manufactured by Saika Chemical Co., Ltd.) was used. The melting point of the composition was 161.1 ° C, and the crystallization temperature was 136.4 ° C. The density of the foam molded article was 0.10 g / cm ³ , and the solid viscoelasticity was 153.1 ° C.
Example 3
100 parts by mass of an ester-based elastomer (trade name: “PELPENE GP-475”, melting point: 147.9 ° C., crystallization temperature: 96.7 ° C., manufactured by Toyobo Co., Ltd.), and an ester-based elastomer resin master batch of isoindoline as a pigment (constitution Resin: 5.0 parts by mass of “PELPENE GP-475”, pigment concentration 10%, manufactured by Saika Chemical Co., Ltd., and 0.3 parts by mass of an organic foam modifier (trade name “Kao Wax EBFF”, manufactured by Kao Corporation) Was supplied to a single screw extruder and melt-kneaded to obtain an ester-based elastomer composition. Thereafter, a foam molded article was obtained in the same manner as in Example 1. The composition had a melting point of 153.7 ° C. and a crystallization temperature of 116.5 ° C. The density of the foam molded article was 0.13 g / cm ³ , and the solid viscoelasticity was 150.8 ° C.
Example 4
Same as Example 3 except that the pigment was changed to a diketopyrrolopyrrole (DPP) ester-based elastomer resin masterbatch (constituting resin: “PELPENE GP-475”, pigment concentration 10% by mass, manufactured by Saika Chemical Co., Ltd.) To obtain a foam molded article. The composition had a melting point of 153.5 ° C and a crystallization temperature of 116.8 ° C. The density of the foam molded article was 0.13 g / cm ³ , and the solid viscoelasticity was 150.5 ° C.

Example 5
A foam molded article was produced in the same manner as in Example 3 except that the pigment was changed to a dichloroquinacridone ester-based elastomer resin masterbatch (constituting resin: “PELPRENE GP-475”, pigment concentration 10% by mass, manufactured by Saika Chemical Co., Ltd.). I got The melting point of the composition was 154.1 ° C, and the crystallization temperature was 122.7 ° C. The density of the foam molded article was 0.13 g / cm ³ , and the solid viscoelasticity was 150.8 ° C.
Example 6
Except that the pigment was changed to 5 parts by mass of a carbon black ester-based elastomer resin masterbatch (constituting resin: “PELPENE GP-475”, pigment concentration: 10% by mass, manufactured by Saika Chemical Co., Ltd.) A foam molded article was obtained. The composition had a melting point of 153.2 ° C and a crystallization temperature of 115.0 ° C. The density of the foam molded article was 0.13 g / cm ³ , and the solid viscoelasticity was 148.3 ° C.
Example 7
Except that the pigment was changed to 10 parts by mass of a carbon black ester-based elastomer resin masterbatch (constituting resin: “PELPRENE GP-475”, pigment concentration 10% by mass, manufactured by Saika Chemical Co., Ltd.), the same as in Example 3 A foam molded article was obtained. The melting point of the composition was 153.9 ° C, and the crystallization temperature was 119.3 ° C. The density of the foam molded article was 0.13 g / cm ³ , and the solid viscoelasticity was 149.5 ° C.
Example 8
Same as Example 3 except that the pigment was changed to 5 parts by mass of a copper phthalocyanine ester-based elastomer resin masterbatch (constituting resin: “PELPENE GP-475”, pigment concentration 10% by mass, manufactured by Saika Chemical Co., Ltd.) A foam molded article was obtained. The composition had a melting point of 152.8 ° C. and a crystallization temperature of 121.9 ° C. The density of the foam molded article was 0.13 g / cm ³ , and the solid viscoelasticity was 148.8 ° C.
Example 9
Except that the pigment was changed to 10 parts by mass of a copper phthalocyanine ester-based elastomer resin masterbatch (constituting resin: “PELPENE GP-475”, pigment concentration: 10% by mass, manufactured by Saika Chemical Co., Ltd.) A foam molded article was obtained. The melting point of the composition was 151.2 ° C, and the crystallization temperature was 122.8 ° C. The density of the foam molded article was 0.13 g / cm ³ , and the solid viscoelasticity was 149.3 ° C.
Example 10
100 parts by mass of an olefin-based elastomer (trade name “R110E”, melting point: 155.6 ° C., crystallization temperature: 101.6 ° C., manufactured by Prime Polymer Co., Ltd.), and an olefin-based elastomer resin master batch of carbon black as a pigment (constituting resin : 2.5 parts by mass of polypropylene, pigment concentration of 20% by mass, manufactured by Toyo Color Co., Ltd. and 0.3 parts by mass of an organic air conditioner (trade name "Kao Wax EBFF", manufactured by Kao Corporation) in a single screw extruder. By supplying and melt-kneading, an olefin-based elastomer composition was obtained. Thereafter, a foam molded article was obtained in the same manner as in Example 1. The composition had a melting point of 153.6 ° C. and a crystallization temperature of 116.3 ° C. The density of the foam molded article was 0.10 g / cm ³ , and the solid viscoelasticity was 150.3 ° C.

Comparative Example 1
100 parts by mass of an amide-based elastomer (trade name: “PEBAX5533”, melting point: 160.1 ° C., crystallization temperature: 124.5 ° C., manufactured by Arkema) having nylon 12 as a hard segment and polytetramethylene glycol as a soft segment; An amide-based elastomer composition was obtained by supplying 0.3 parts by mass of a system foam adjuster (trade name “Kao Wax EBFF”, manufactured by Kao Corporation) to a single-screw extruder and melt-kneading. Thereafter, a foam molded article was obtained in the same manner as in Example 1. The density of the foam molded article was 0.10 g / cm ³ , and the solid viscoelasticity was 146.0 ° C.
Comparative Example 2
100 parts by mass of an ester-based elastomer (trade name: “PELPENE GP-475”, melting point: 147.9 ° C., crystallization temperature: 96.7 ° C., manufactured by Toyobo Co., Ltd.), and an organic foam regulator (trade name: “Kao Wax EBFF”) 0.3 part by mass (manufactured by Kao Corporation) was supplied to a single screw extruder and melt-kneaded to obtain an ester-based elastomer composition. Thereafter, a foam molded article was obtained in the same manner as in Example 1. The density of the foam molded article was 0.13 g / cm ³ , and the solid viscoelasticity was 146.6 ° C.
Comparative Example 3
100 parts by mass of an olefin-based elastomer (trade name “R110E”, melting point 155.6 ° C., crystallization temperature 101.6 ° C., manufactured by Prime Polymer Co., Ltd.), and an organic foam control agent (trade name “Kao Wax EBFF”, Kao Corporation) Was supplied to a single-screw extruder and melt-kneaded to obtain an olefin-based elastomer composition. Thereafter, a foam molded article was obtained in the same manner as in Example 1. The density of the foam molded article was 0.10 g / cm ³ , and the solid viscoelasticity was 146.2 ° C.
Table 1 shows the production conditions and various physical properties of Examples 1 to 10 and Comparative Examples 1 to 4. In the table, AE is an amide elastomer, EE is an ester elastomer, OE is an olefin elastomer, CB is carbon black, CuP is copper phthalocyanine, Iso I is isoindoline, DPP is diketopyrrolopyrrole, and diClQ is dichloroquinacridone. means.

  Table 1 shows that the foamed article obtained from the composition containing the pigment exhibits improved heat resistance (solid viscoelasticity) compared to the foamed article containing no pigment.

Claims (10)

  A thermoplastic elastomer composition comprising: a thermoplastic elastomer; and a pigment as a heat resistance improver.   The thermoplastic elastomer composition according to claim 1, wherein the pigment is contained in an amount of 0.05 to 3.0 parts by mass based on 100 parts by mass of the thermoplastic elastomer.   The thermoplastic elastomer composition according to claim 1, wherein the thermoplastic elastomer exhibits crystallinity and is selected from an amide-based elastomer, an olefin-based elastomer, an ester-based elastomer, and a urethane-based elastomer.   The thermoplastic elastomer composition according to any one of claims 1 to 3, wherein the thermoplastic elastomer is an amide-based elastomer, and the thermoplastic elastomer composition has a melting point higher by 20 to 30C than a crystallization temperature. .   The thermoplastic elastomer composition according to any one of claims 1 to 3, wherein the thermoplastic elastomer is an olefin-based elastomer, and the thermoplastic elastomer composition has a melting point higher by 30 to 45 ° C than a crystallization temperature. .   The thermoplastic elastomer composition according to any one of claims 1 to 3, wherein the thermoplastic elastomer is an ester elastomer, and the thermoplastic elastomer composition has a melting point higher by 25 to 45 ° C than a crystallization temperature. .   Expanded particles containing a thermoplastic elastomer composition containing a thermoplastic elastomer and a pigment as a heat resistance improver as a base resin.   The foamed particles according to claim 7, wherein the foamed particles have a bulk density of 0.05 to 0.5 g / cm3, an open cell ratio of 10% or less, and an average particle diameter of 1 to 10 mm.   A foam molded article using a thermoplastic elastomer composition containing a thermoplastic elastomer and a pigment as a heat resistance improver as a base resin.   The foam molded article according to claim 9, wherein the foam molded article is used as a building material, a shoe member, or a cushioning material.