JP2002294006A - Thermoplastic elastomer composition - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a thermoplastic elastomer composition excellent in scratch resistance wear resistance and mechanical properties (especially elongation at break). SOLUTION: This thermoplastic elastomer composition comprises the components (A) to (C) shown below; (A): an ethylene and/or α-olefin-aromatic vinyl compound copolymer, (B): an ethylene->=4C α-olefin copolymer and (C): an olefin-based resin.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

[0001] The present invention relates to a thermoplastic elastomer composition. More specifically, the present invention relates to scratch resistance, abrasion resistance and mechanical properties (particularly elongation at break).
The present invention relates to a thermoplastic elastomer composition having excellent heat resistance.

[0002]

2. Description of the Related Art Conventionally, since a molded article molded using a thermoplastic elastomer is used after being painted, scratch resistance and abrasion resistance are imparted by a coating film, so that a thermoplastic elastomer is not required. Was. In recent years, the number of molded articles to be coated has decreased, and scratch resistance and abrasion resistance have been emphasized, and the required performance thereof has been further enhanced. Further, since the strength of the molded body is also required, the mechanical properties of the material are also required. In light of the current situation, conventional thermoplastic elastomer compositions have not always been satisfactory.

[0003]

Under these circumstances, an object of the present invention is to provide a thermoplastic elastomer composition having excellent scratch resistance, abrasion resistance and mechanical properties (particularly elongation at break). It is in the point of doing.

[0004]

That is, the present invention relates to a thermoplastic elastomer composition containing the following components (A) to (C). (A): ethylene and / or α-olefin-aromatic vinyl compound copolymer (B): ethylene-α-olefin copolymer composed of α-olefin having 4 or more carbon atoms (C): olefin resin

[0005]

DETAILED DESCRIPTION OF THE INVENTION Component (A) of the present invention is an ethylene and / or α-olefin-aromatic vinyl compound copolymer.

Here, the α-olefin includes propylene, 1-butene, 1-pentene, 1-hexene, 4-methyl-1-pentene, 1-octene, 1-decene and the like. -Butene, 1-hexene and 1-octene are preferred. Examples of the aromatic vinyl compound include p-methylstyrene, m-methylstyrene,
o-methylstyrene, p-ethylstyrene, m-ethylstyrene, o-ethylstyrene, 2,4-dimethylstyrene, 2,5-dimethylstyrene, 3,4-dimethylstyrene, 3,5-dimethylstyrene, 3- Methyl-5
Ethyl styrene, p-tert-butyl styrene, p-
alkylstyrene such as sec-butylstyrene; styrene, 2-phenyl-1-propylene, 2-phenyl-
Examples thereof include alkenylbenzenes such as 1-butene; bisalkenylbenzenes such as divinylbenzene; vinylnaphthalenes such as 1-vinylnaphthalene. Among these alkenyl aromatic compounds, ease of synthesis and copolymerizability (easy to produce as a monomer,
And copolymerization with ethylene or α-olefin is easy).
Methylstyrene, o-methylstyrene, p-tert-
Butylstyrene, 2-phenylpropylene, divinylbenzene and 1-vinylnaphthalene are preferred, with styrene being particularly preferred. The content of the aromatic vinyl compound is 5 to 5
0% by weight, more preferably 10 to 10% by weight.
35% by weight. If the content of the aromatic vinyl compound is too small, the elasticity and transparency may be poor. On the other hand, if the content is too large, the elasticity may be poor. As the component (A) of the present invention, an ethylene-aromatic vinyl compound copolymer is particularly preferred from the viewpoint of flexibility and elastic recovery.

The component (B) according to the present invention comprises α-α having 4 or more carbon atoms.
It is an ethylene-α-olefin copolymer composed of olefin. The melt flow rate (190 ° C., 21.18 N) of the ethylene-α-olefin copolymer is 0.01 to 1
It is preferably 00 g / 10 min, more preferably 0.1 to 30 g / 10 min. If the melt flow rate is too small, the moldability is poor, while if the melt flow rate is too large, the mechanical properties may be significantly reduced.

The α-olefin having 4 or more carbon atoms includes
Examples thereof include 1-butene, 1-pentene, 1-hexene, 4-methyl-1-pentene, 1-octene, and 1-decene, and among them, 1-butene, 1-hexene and 1-octene are preferred. The content of the α-olefin is 5 to 50% by weight, preferably 10 to 40% by weight.

The component (C) of the present invention is an olefin resin. Examples of the olefin-based resin include an ethylene-based resin, a propylene-based resin, and a butene-based resin, and may be a single substance or a mixture. As olefin resin, heat resistance,
From the viewpoint of industrialization, a propylene-based resin is preferred. Melt flow rate of olefin resin (230 ° C, 21.
18N) is preferably 0.1 to 150 g / 10 min, more preferably 1 to 100 g / 10 min. If the melt flow rate is too small, the moldability is poor, while if the melt flow rate is too large, the mechanical properties may be significantly reduced. Examples of the propylene-based resin include homopolypropylene (C1), propylene-ethylene random copolymer (C2), and propylene-ethylene block copolymer (C3). Further, a mixture of (C1), (C2) and (C3) may be used.

(C1) is a homopolymer of propylene, and if it is desired to increase the rigidity, a polymer having high crystallinity is preferable.

(C2) is a copolymer obtained by randomly polymerizing propylene and ethylene. When it is desired to increase the rigidity, it is preferable to reduce the ethylene content or to have high crystallinity. Conversely, when it is desired to lower the rigidity, it is preferable to increase the ethylene content or lower the crystallinity.

(C3) is a block copolymer comprising a first segment and a second segment, wherein the first segment is a homopropylene portion of propylene homopolymerization and the second segment is a propylene-ethylene random copolymer portion. is there. As the first segment, a propylene-ethylene random copolymer having a different ethylene content from the second segment may be used. Further, the content of the propylene-ethylene random copolymer part as the second segment is 30.
You may use the reactor olefin-type thermoplastic elastomer (R-TPO) which is more than weight%. When it is desired to increase the rigidity, those having a small content of the propylene-ethylene random copolymer portion as the second segment and those having a small ethylene content of the propylene-ethylene random copolymer portion are preferable. Conversely, when it is desired to lower the rigidity, those having a high content of the propylene-ethylene random copolymer portion as the second segment and those having a high ethylene content of the propylene-ethylene random copolymer portion are preferable.

The preferred content of each component in the thermoplastic elastomer composition of the present invention is such that the content of (A) is 10%.
-80% by weight, the content of (B) is 10-80% by weight, and the content of (C) is 60-10% by weight (provided that (A) + (B) + ( C) = 100 parts by weight.) If (A) is too small, scratch resistance and abrasion resistance may be poor, while if (A) is too large, mechanical properties may be poor. If the content of (B) is too small, the mechanical properties may be poor. On the other hand, if the content of (B) is too large, the scratch resistance and abrasion resistance may be poor.
If the content of (C) is too small, the fluidity may be reduced and the moldability may be poor. On the other hand, if the content of (C) is too large, the scratch resistance and abrasion resistance may be poor.

[0014] The thermoplastic elastomer composition of the present invention comprises:
In addition to the essential components (A) to (C), inorganic fillers (talc, calcium carbonate, calcined kaolin, etc.), organic fillers (fiber, wood powder, cellulose powder, etc.), lubricants (fatty acid amides, etc.), oxidation Inhibitors (phenol-based, sulfur-based, phosphorus-based, lactone-based, vitamin-based, etc.), weather stabilizers, ultraviolet absorbers (benzotriazole-based, triazine-based, anilide-based, benzophenone-based, etc.), heat stabilizers, light stabilizers (Hindered amines, benzoates, etc.), pigments and the like. In order to further improve the wear resistance, it is preferable to contain an inorganic filler. Further, it is more preferable to contain an inorganic filler and a lubricant. Calcium carbonate is preferred for flexible thermoplastic elastomer compositions.

In order to obtain the thermoplastic elastomer composition of the present invention, melt kneading may be performed using a continuous or batch kneader. Examples of the continuous kneader include a single screw extruder and a twin screw extruder, and examples of the batch kneader include a kneader and a Banbury mixer. Component (A)
Depending on the shape of (C), a batch type or a continuous type may be used together.

The thermoplastic elastomer of the present invention is used for extrusion molding, injection molding, press molding, blow molding, powder molding and the like. It is preferably used for applications such as automobiles, railways, airplanes, ships, and the like, home electric appliance components, civil engineering and construction components, stationery, miscellaneous goods, and the like, which have scratch resistance and wear resistance.

The thermoplastic elastomer composition of the present invention comprises:
As a preferred specific example of the multilayer molded article used in the multilayer molding and the sheet, a molded article in which the core portion is an olefin-based resin and the skin portion is molded by two-layer molding comprising the thermoplastic elastomer composition of the present invention is given. be able to. When a soft feeling is required for the skin portion, the hardness (shoreA) of the thermoplastic elastomer composition is preferably 99 or less. More preferably, the hardness (shoreA) is 90-60.
Examples of the olefin resin in the core include propylene resins, ethylene resins, and olefin thermoplastic elastomers.

In order to obtain a molded article formed by the above-described two-layer molding, for example, coextrusion by an extruder, two-color molding by injection molding, insert molding and the like may be performed.

Preferred examples of the multilayer molded body include automobile interior parts, and specifically include an instrument panel, a door, an armrest, a grab rail, a shift knob, an instrument panel grip, a side brake knob, a console box, a glass run, Weather strips and the like.

[0020]

The following examples illustrate the invention in more detail. [I] Raw material (A) Ethylene-aromatic vinyl compound copolymer Ethylene and styrene were continuously copolymerized using a 100 L SUS polymerization vessel equipped with stirring blades. That is, 84.7 hexane was used as a polymerization solvent from the bottom of the polymerization vessel.
kg / h, ethylene 2.8 kg / h, styrene 4.
Feed continuously at a rate of 15 kg / hour. On the other hand, the polymerization liquid is continuously withdrawn from the upper part of the polymerization vessel so that the polymerization liquid in the polymerization vessel becomes 100 L. As a catalyst, isopropylidene (cyclopentadienyl) (3-tert-butyl-5) is used.
-Methyl-2-phenoxy) titanium dichloride,
N, N-dimethylanilinium tetrakis (pentafluorophenyl) borate and triisobutylaluminum were continuously fed from the lower part of the polymerization reactor into the polymerization reactor at a rate of 0.348 g / hr, 1.081 g / hr, and 6.912 g / hr, respectively. Supplied. The copolymerization reaction is performed by circulating cooling water through a jacket attached to the outside of the polymerization vessel.
Performed at 0 ° C. A small amount of ethanol was added to the polymerization solution withdrawn from the polymerization vessel to stop the polymerization reaction,
After washing with water, the solvent was removed by steam in a large amount of water, and the copolymer was taken out and dried at 80 ° C. under reduced pressure day and night. By the above operation, ethylene-styrene copolymerization was performed at a rate of 2 kg / hour. The intrinsic viscosity [η] of this copolymer measured at 135 ° C. using tetralin as a solvent with an Ubbelohde viscometer was 2.31. When a melting curve was determined at a heating rate of 10 ° C./min using a differential thermal analyzer (DSC220 manufactured by Seiko Instruments Inc.), the melting point was 44.
℃, the glass transition point was -20 ℃. ¹³ C-NMR
(JNM-EX270 manufactured by JEOL Ltd., measurement solvent orthodichlorobenzene, measurement temperature: 135 ° C.) The styrene content determined by analysis was 16 mol%, and 36.0 to 3
34.0 to the area of the peak appearing at 8.0 ppm
The ratio of the areas of the peaks appearing at 36.0 ppm is 0.01
Nine. (B-1) Ethylene-α-olefin copolymer MFR (190 ° C., 21.18 N) = 0.6 g / 10 m
Ethylene-butene copolymer which is in (B-2) Ethylene-α-olefin copolymer MFR (190 ° C., 21.18 N) = 0.7 g / 10 m
ethylene-propylene copolymer (C) olefin-based resin MFR (230 ° C., 21.18 N) = 65 g / 10 mi
n is a propylene-ethylene block copolymer

[II] Measurement Method The obtained composition was molded at 200 ° C. using a press molding machine into a flat plate having a thickness of 2 mm and a size of 150 mm × 150 mm, and then required measurements were performed. (1) Scratch resistance test Using a surface property measuring device Tribogear (manufactured by Shinto Kagaku Co.), 30
Scratches were made by scratching the mirror surface of the plate formed by pressing with a scratch needle loaded with a load of 0 g at a constant speed, and the scratches were evaluated by visual observation. ○: good (scratch is not conspicuous) ×: bad (scratch is conspicuous) (2) Abrasion test A cloth (Kanakin No. 3) and a plate are attached to a Gakushin abrasion tester, a load of 500 g is placed, and the mirror surface is clothed with a cloth. The surface worn by rubbing 200 times was evaluated by visual observation. ；: Good (abrasion is not conspicuous) ×: bad (abrasion is conspicuous) (3) Tensile test A test piece was punched out from a press-formed plate using a JIS No. 3 dumbbell, and the speed was 200 m using a tensile tester.
The sample was pulled at m / min, and the breaking strength and the breaking elongation were measured.
(Based on JIS K6251.)

Example 1 and Comparative Examples 1 to 3 The compositions shown in Table 1 were melt-kneaded in a Labo Plastomill. The obtained composition was molded and measured. The results are shown in Table 1.

[0023]

[Table 1]

[0024]

As described above, according to the present invention, a thermoplastic elastomer composition having excellent scratch resistance, abrasion resistance and mechanical properties (particularly elongation at break) can be provided.

 ──────────────────────────────────────────────────続 き Continuing on the front page F term (reference) 4F100 AK03A AK03B AK03C AK04A AK04C AK07A AK07C AK11A AK11C AK12A AK12C AL01A AL01C AL05A AL05C AL09A AL09C BA03 BA06 JB16A JB16C JK08 JWB BB00 JB00B

Claims (6)

[Claims] 1. A thermoplastic elastomer composition comprising the following components (A) to (C). (A): ethylene and / or α-olefin-aromatic vinyl compound copolymer (B): ethylene-α-olefin copolymer composed of α-olefin having 4 or more carbon atoms (C): olefin resin 2. The thermoplastic elastomer composition according to claim 1, wherein the aromatic vinyl compound (A) is styrene. 3. The thermoplastic elastomer composition according to claim 1, wherein (C) is a propylene-based resin. 4. The content of (A) is from 10 to 80% by weight, the content of (B) is from 10 to 80% by weight, and the content of (C) is from 60 to 10% by weight. The thermoplastic elastomer composition according to claim 1, wherein (A) + (B) + (C) = 100% by weight. 5. The thermoplastic elastomer composition according to claim 1, which is used for multilayer molding and a sheet. 6. A multilayer molded article comprising a core part made of an olefin resin and a surface part made of the thermoplastic elastomer composition according to claim 1.