KR101843748B1 - Polypropylene resin composition and article prepared therefrom - Google Patents

Abstract

A polypropylene resin composition for injection foaming which is excellent in light weight due to foaming and excellent in mechanical properties, dimensional stability and injection appearance, and a molded article produced thereby.
The polypropylene resin composition according to one embodiment comprises 33 to 93% by weight of a polypropylene resin, based on the total weight of the polypropylene resin composition; 1 to 30% by weight of a thermoplastic elastomer; 1 to 30% by weight of inorganic filler; 0.1 to 2% by weight of a sodium phosphate-based nucleating agent; And 0.1 to 3% by weight of a foaming agent.

Description

BACKGROUND OF THE INVENTION 1. Field of the Invention [0001] The present invention relates to a polypropylene resin composition,

The disclosed invention relates to a polypropylene resin composition used for injection foaming and a molded article produced therefrom.

Since the weight of the vehicle has a close relationship with the fuel consumption performance and the driving performance, a continuous effort is made to reduce the weight of the vehicle.

Thermoplastics are mainly used in vehicles. Previously, polyvinyl chloride (PVC) has been widely used as a vehicle interior material such as door trim and dashboard, but it has a problem of emitting harmful substances in a specific environment.

Therefore, recently, polypropylene, a thermoplastic polyolefin-based polymer that does not emit harmful substances, has emerged as an important material that can replace PVC in automobile interior materials. In addition, polypropylene has a lower density than polyvinyl chloride and can be used to lighten the vehicle when it is used.

A polypropylene resin composition for injection foaming which is excellent in light weight due to foaming and excellent in mechanical properties, dimensional stability and injection appearance, and a molded article produced thereby.

The polypropylene resin composition according to one embodiment comprises 33 to 93% by weight of a polypropylene resin, based on the total weight of the polypropylene resin composition; 1 to 30% by weight of a thermoplastic elastomer; 1 to 30% by weight of inorganic filler; 0.1 to 2% by weight of a sodium phosphate-based nucleating agent; And 0.1 to 3% by weight of a foaming agent.

The polypropylene resin may include at least one of a propylene homopolymer and a propylene-ethylene copolymer.

The propylene homopolymer may be contained in a proportion of 0 to 30% by weight based on the total weight of the polypropylene resin, and the propylene-ethylene copolymer may be included in a proportion of 70 to 100% by weight based on the total weight of the polypropylene resin.

The propylene homopolymer may be contained in a proportion of 0 to 20% by weight based on the total weight of the polypropylene resin, and the propylene-ethylene copolymer may be included in a proportion of 80 to 100% by weight based on the total weight of the polypropylene resin.

The propylene homopolymer may have a melt index (Melt Index) of 1 to 100 g / 10 min measured at 230 ° C under a load of 2.16 kg.

The propylene-ethylene copolymer may have a melt index of 1 to 100 g / 10 min measured at 230 ° C under a load of 2.16 kg

The thermoplastic elastomer may include at least one of an ethylene-alpha olefin copolymer having 4 or more carbon atoms and a styrene-diene copolymer.

The alpha-olefin copolymer having four or more ethylene-carbon atoms may include at least one of an ethylene butene-1 copolymer (EBM) and an ethylene octene-1 copolymer (EOM).

The alpha olefin copolymer having 4 or more carbon atoms may be contained in an amount of 12 to 45% by weight based on the total weight of the thermoplastic elastomer.

The styrene-diene copolymer may be a styrene-butylene-styrene block copolymer, a styrene-ethylene-butylene-styrene block copolymer, a styrene-isoprene-styrene block copolymer, a styrene- - ethylene-propylene-styrene block copolymer.

The thermoplastic elastomer may have a melt index of 10 to 40 g / 10 min measured at 230 DEG C under a load of 2.16 kg.

The thermoplastic elastomer may be contained in an amount of 3 to 5% by weight based on the total weight of the polypropylene resin composition.

The inorganic filler may include at least one of a fibrous inorganic filler and a non-fibrous inorganic filler.

The fiber-based inorganic filler may have an average fiber length of 1 to 5 mm.

The fibrous inorganic filler may include at least one of glass fiber, carbon fiber and metal fiber.

The non-fibrous inorganic filler may include at least one of talc, calcium carbonate, barium sulfate, glass bubbles, and glass beads.

The sodium phosphate-based nucleating agent can be represented by the following formula (1).

[Chemical Formula 1]

R and R 'are each a hydrogen atom or a substituted or unsubstituted alkyl group.

The alkyl group may be substituted with at least one functional group selected from a vinyl group, an amino group, a methacrylic group, an epoxy group, a mercapto group, a phenol group and a phenyl group.

The molded article according to one embodiment is produced by a polypropylene resin composition.

The foaming agent may be mixed in a proportion of 0.5 to 1.5% by weight.

The molded article may be at least one of the interior material of the vehicle and the exterior material of the vehicle.

According to the polypropylene resin composition and the molded article produced thereby, the polypropylene resin composition according to one embodiment is excellent in light weight due to foaming and excellent in mechanical properties, dimensional stability, and appearance of injection.

BRIEF DESCRIPTION OF DRAWINGS FIG. 1 is a view showing an example in which a molded article produced by a polypropylene resin composition is used as a casing of a vehicle.
Fig. 2 is a view showing an example in which a molded article produced by the polypropylene resin composition is used as an interior material of a vehicle.

Hereinafter, examples of a polypropylene resin composition and a molded article produced thereby will be described in detail with reference to the accompanying drawings, formulas and tables.

A thermoplastic polyolefin-based polymer which does not discharge harmful substances to exterior materials such as door trim of vehicles, interior materials such as dashboards, and bumpers can be used. In particular, polypropylene has a density lower than a polyvinyl chloride (PVC) having a density of 0.855 g / cm ^3, a bar having a density of 0.946 g / cm ³ in the determination area, from 1.1 to 1.45 g / cm ³ in non region Therefore, when the polypropylene resin composition is used as a vehicle interior or exterior material, the weight of the vehicle can be reduced.

Further, when the polypropylene resin composition is processed by foam molding, the lightening effect can be maximized.

The polypropylene resin composition according to one embodiment has a composition capable of obtaining an excellent appearance while foaming and injection are performed stably.

The polypropylene resin composition according to one embodiment comprises (A) 33 to 93% by weight of a polypropylene resin, (B) 1 to 30% by weight of a thermoplastic elastomer, (C) 1 to 30% by weight of an inorganic filler, (D) 0.1 to 2% by weight of a nucleating agent and (E) 0.1 to 3% by weight of a blowing agent. Hereinafter, each component constituting the polypropylene resin composition according to one embodiment will be described in detail.

(A) Polypropylene resin

The polypropylene resin may be a crystalline polymer containing at least one of a propylene homopolymer (A1) containing a propylene monomer as a main component and a propylene-ethylene copolymer (A2) containing ethylene.

Each of the propylene homopolymer and the propylene-ethylene copolymer may be used alone, or a mixture of a propylene homopolymer and a propylene-ethylene copolymer may be used.

The propylene homopolymer (A1) may have a melt index (MI) of 1 to 100 g / 10 min measured at 230 ° C under a load of 2.16 kg. The melt index is an index indicating the melt flowability of a plastic material having a constant load and a constant temperature. In the polypropylene resin composition according to one embodiment, a suitable range of melt index can be selected in consideration of both the expansion ratio and the mechanical properties.

When a propylene homopolymer having a melt index of 1 to 100 g / 10 min at 230 DEG C and a load of 2.16 kg is used, excellent foamability and excellent mechanical and impact properties can be ensured. In addition, it is possible to prevent defects due to surface gas which may occur during injection molding.

The propylene-ethylene copolymer (A2) may have a melt index (Melt Index) of 1 to 100 g / 10 min measured at 230 ° C under a load of 2.16 kg. When a propylene homopolymer having a melt index of 1 to 100 g / 10 min at 230 DEG C under a load of 2.16 kg is used in the same manner as the propylene homopolymer (A1), excellent foamability and excellent mechanical and impact properties are ensured . In addition, it is possible to prevent defects due to surface gas which may occur during injection molding.

When a mixture of a propylene homopolymer and a propylene-ethylene copolymer is used, the mixing ratio of the propylene homopolymer to the propylene-ethylene copolymer ranges from 0 to 30% by weight of the propylene homopolymer and from 100 to 70% by weight of the propylene- Lt; / RTI >

Alternatively, 100 to 80% by weight of the propylene-ethylene copolymer may be blended with respect to 0 to 20% by weight of the propylene homopolymer.

The propylene homopolymer and the propylene-ethylene copolymer may be mixed to complement each other with insufficient physical properties. This ensures excellent impact strength and fluidity. The impact resistance can be improved by the propylene-ethylene copolymer to improve the impact strength, and the propylene homopolymer can complement the physical properties such as moldability, rigidity and heat resistance.

The content ratio of the polypropylene resin containing at least one of propylene homopolymer and propylene-ethylene copolymer can be determined in consideration of physical properties such as fluidity, rigidity and impact strength of the polypropylene resin composition. For example, the lower limit value of the content ratio can be determined in consideration of the workability at the time of product injection based on flowability and flowability, and the upper limit value of the content ratio can be determined in consideration of physical properties such as stiffness and impact strength.

As described above, when the polypropylene resin is contained in the polypropylene resin composition in a proportion of 33 to 93% by weight, properties such as excellent flowability, workability, rigidity and impact strength can be obtained.

(B) a thermoplastic elastomer

The thermoplastic elastomer (B) may be included for ensuring processability, rebound resilience, heat resistance and impact resistance of the polypropylene resin composition according to one embodiment.

The thermoplastic elastomer (B) may comprise at least one of an ethylene-alpha-olefin copolymer and a styrene-diene copolymer. That is, the ethylene-alpha olefin copolymer may be used alone as the thermoplastic elastomer, the styrene-diene copolymer may be used alone, or a mixture of the ethylene-alpha olefin copolymer and the styrene-diene copolymer may be used It is possible.

For example, the alpha olefins used in the preparation of ethylene-alpha olefin copolymers may be alpha olefins having 4 or more carbon atoms. Specifically, an ethylene-butene-1 copolymer (EBM) or an ethylene-octene-1 copolymer (ethylene-octene-1 copolymer: EOM) is used as an alpha olefin copolymer having four or more ethylene- And the content of alpha olefin in the copolymer is 12 to 45% by weight.

As the styrene-based monomer in the styrene-diene copolymer, styrene,? -Methylstyrene,? -Ethylstyrene, p-methylstyrene and the like can be used Butadiene, isoprene, and the like can be used as the diene-based monomer.

When the above-mentioned styrene-based monomer or diene-based monomer is used, excellent workability, impact resistance, rebound resilience and heat resistance can be secured.

Examples of the styrene-diene-based copolymer include styrene-butylene-styrene block copolymer, styrene-ethylene-butylene-styrene block copolymer, styrene-isoprene-styrene block copolymer, styrene- And a styrene-ethylene-propylene-styrene block copolymer may be used.

On the other hand, the thermoplastic elastomer (B) may be a thermoplastic elastomer having a melt index (MI) of 10 to 40 g / 10 min measured at 230 DEG C under a load of 2.16 kg. The range of the melt index of the thermoplastic elastomer can be determined by considering the flowability, and the upper limit value can be determined in consideration of physical properties such as impact resistance and surface impact resistance.

By selecting a melt index of 10 g / 10 min or more, the problem of poor flowability and poor dispersion can be prevented. By selecting a melt index of 40 g / 10 min or less, deterioration of impact resistance and surface impact resistance can be prevented.

As described above, the thermoplastic elastomer (B) may be contained in an amount of 1 to 30% by weight based on the total weight of the polypropylene resin composition. By containing the thermoplastic elastomer (B) in an amount of 1% by weight or more, the impact resistance can be prevented from lowering, and the content of the thermoplastic elastomer (B) is 30% by weight or less.

Alternatively, the thermoplastic elastomer (B) may be contained in an amount of 3 to 25% by weight based on the total weight of the polypropylene resin composition.

(C) Inorganic filler

The inorganic filler (C) may be included to improve the rigidity, impact resistance and heat resistance of the polypropylene resin composition according to one embodiment.

As the inorganic filler (C), at least one of a fibrous inorganic filler and a non-fibrous inorganic filler may be used.

As one example, at least one of glass fiber, carbon fiber and metal fiber may be used as the fiber-based inorganic filler. The average fiber length (L) of the fiber-based inorganic filler may be selected in the range of 1 to 5 mm, and the maximum aspect ratio may be selected in the range of 50 to 300.

When the average fiber length and the maximum aspect ratio are selected in the above-mentioned range, excellent impact resistance and rigidity can be obtained while securing excellent flowability and moldability.

For example, at least one of talc, calcium carbonate, barium sulfate, glass bubbles and glass beads may be used as the non-fibrous inorganic filler.

(D) Sodium Phosphate Nucleating Agent

The sodium phosphate-based nucleating agent (D) may be included in order to prevent stiffness, heat resistance of the polypropylene resin composition according to one embodiment, and formation of gas marks on the injection surface due to foaming during injection molding.

For example, the sodium phosphate-based nucleating agent (D) is characterized by being represented by the following formula

  [Chemical Formula 1]

In the above formula (1), R and R 'may be a hydrogen atom, a substituted or unsubstituted alkyl group, and R and R' may be the same or different. The substituent (Y) may be a functional group such as a vinyl group, an amino group, a methacrylic group, an epoxy group, a mercapto group, a phenol group or a phenyl group.

In one example, R, R 'may be bis (2,4-Di-tert-butyl phenol) or bis (4-tert-butyl phenyl).

For example, the sodium phosphate-based nucleating agent (D) may be contained in an amount of 0.1 to 2% by weight based on the polypropylene resin composition. It is possible to ensure nucleation of the polypropylene resin sufficiently by incorporating 0.1 wt% or more of the sodium phosphate-based nucleating agent (D), and when the nucleation of the polypropylene resin is sufficiently carried out, excellent tensile strength and bending strength can be obtained.

Particularly, when nucleation is not sufficiently performed on the surface of the mold at the time of foaming injection, the surface is not solidified and the foaming gas is transferred to the surface and the appearance of the injection may become poor. When the nucleation agent (D) So that this problem can be avoided. In addition, 2% by weight or less of the sodium phosphate-based nucleating agent (D) is contained, and an excellent impact strength can be obtained. It is also possible that the sodium phosphate-based nucleating agent (D) is contained in an amount of 0.5 to 1.5% by weight.

(E) foaming agent

The foaming agent (E) may be included in the foaming injection processing of the polypropylene resin composition according to one embodiment to form a foamed cell in the article.

As an example, the blowing agent (E) may comprise sodium hydrogen bicarbonate.

For example, the foaming agent (E) may be contained in an amount of 0.1 to 3% by weight based on the polypropylene resin composition. When the foaming agent (E) is contained in an amount of 0.1 wt% or more, foaming cells can be sufficiently formed during injection molding, and the foaming cells can be uniformly formed by 3 wt% or less. In addition, by preventing the excessive generation of the foaming gas, it is possible to prevent a gas mark from appearing on the appearance of the article due to the excessively generated foaming gas. Further, it is possible to prevent the mechanical strength from being lowered due to excessive generation of the foaming gas.

It is also possible that the foaming agent (E) is contained in an amount of 0.5 to 1.5% by weight.

Meanwhile, the polypropylene resin composition according to one embodiment may further include conventional additives. For example, additives such as an antioxidant, an antistatic agent and the like may be included in an appropriate amount range.

Examples of the antioxidant include a phenolic antioxidant, a phosphite-based antioxidant, and a thiodipropinone synergist.

It is also possible to further include other additives in addition to the antioxidant and the antistatic agent, and the use of the additives can be easily performed by those skilled in the art.

The polypropylene resin composition according to one embodiment may be produced by mixing a polypropylene resin (A), a thermoplastic elastomer (B), a polypropylene resin (B) and a thermoplastic elastomer (B) in accordance with the composition ratio described above using a kneader such as a single screw extruder, a twin screw extruder, a multi-screw extruder, a Banbury mixer, , (C) an inorganic filler, (D) a sodium phosphate-based nucleating agent, and (E) a foaming agent.

However, the method for producing the polypropylene resin composition according to one embodiment is not limited thereto, and the polypropylene resin composition can be prepared by mixing the components using various methods other than the above-mentioned methods.

The molded article according to one embodiment can be produced by molding the polypropylene resin composition according to the above-described embodiment. For example, a foam molding process can be used to realize a lightweight molded article. Various molding methods such as extrusion molding, compression molding, injection molding, and the like are applied to the polypropylene resin composition according to the above-described embodiment for foam molding Whereby a molded article having a desired shape can be produced.

When the polypropylene resin composition according to one embodiment is injected into a mold and high temperature steam is injected into the mold, a molded article having the shape of the mold can be produced while the mixture is expanded. However, it is obvious to a person skilled in the art that a molded article can be manufactured by applying various manufacturing methods to the molded article using the polypropylene resin composition.

Hereinafter, the properties of the present invention will be described by way of various examples and comparative examples of the molded article produced by the above-mentioned polypropylene resin composition. However, the following examples are provided to aid understanding of the present invention, and the scope of the present invention is not limited to the following examples.

≪ Example 1 and Comparative Examples 1 to 4 >

(A) a polypropylene resin, (B) a thermoplastic elastomer, (C) an inorganic filler, (D) a nucleating agent and (E) a foaming agent were prepared for producing a polypropylene resin composition.

(A) Polypropylene resin

(A1) Propylene homopolymer: A melt index of 11 g / 10 min as measured at 230 ° C under a load of 2.16 kg was used.

(A2) Propylene-ethylene copolymer: A melt index of 90 g / 10 min as measured at 230 ° C under a load of 2.16 kg was used.

(B) a thermoplastic elastomer

A thermoplastic elastomer containing an ethylene octene-1 copolymer (EOM) having a melt index of 15 g / 10 min measured at 230 DEG C under a load of 2.16 kg was used.

(C) Inorganic filler

Talc having a number average particle size of 2 탆 was used.

(D) Nucleating agent

(D1) First nucleating agent: methylene bis- (2,4-di-tert-butylphenol) acid phosphate sodium saltmetylene bis- (2,4-di-tert-butylphenol) .

(D2) Second nucleating agent: Dibenzylidene sorbitol was used.

(E) Foaming agent: sodium hydrogen bicarbonate was used.

Example  One

(A) 15 wt% of propylene homopolymer, (A2) 47 wt% of propylene-ethylene copolymer, (B) 15 wt% of thermoplastic elastomer, (C) 20 wt% of inorganic filler, The mixture was mixed to prepare a polypropylene resin composition, which was then extruded using a twin-screw extruder. The extruded pellets were mixed with 2% by weight of sodium hydrogen bicarbonate (E) as a foaming agent (E) and injection-molded using a core-back mold to prepare specimens. The component ratios in the Examples and Comparative Examples are based on the total weight of the mixture of the polypropylene resin composition and the foaming agent.

Comparative Example  One

(A) 15 wt% of propylene homopolymer, (A2) 48 wt% of propylene-ethylene copolymer, 15 wt% of thermoplastic elastomer (B) and 20 wt% of inorganic filler (C) were mixed to prepare a polypropylene resin composition , And extruded using a twin-screw extruder. The extruded pellets were mixed with 2% by weight of sodium hydrogen bicarbonate (E) as a foaming agent (E) and injection-molded using a core-back mold to prepare specimens. No nucleating agent was included.

Comparative Example  2

(A) 15 wt% of propylene homopolymer, (A2) 44 wt% of propylene-ethylene copolymer, (B) 15 wt% of thermoplastic elastomer, (C) 20 wt% of inorganic filler, The mixture was mixed to prepare a polypropylene resin composition, which was then extruded using a twin-screw extruder. The extruded pellets were mixed with 2% by weight of sodium hydrogen bicarbonate (E) as a foaming agent (E) and injection-molded using a core-back mold to prepare specimens.

Comparative Example  3

(A) 15 wt% of propylene homopolymer, (A2) 44 wt% of propylene-ethylene copolymer, (B) 15 wt% of thermoplastic elastomer, (C) 20 wt% of inorganic filler, and (D1) The mixture was mixed to prepare a polypropylene resin composition, which was then extruded using a twin-screw extruder. The extruded pellets were mixed with 5% by weight of sodium hydrogen bicarbonate (E) as a foaming agent (E) and injection-molded using a core-back mold to prepare specimens.

Comparative Example  4

(A) 15 wt% of propylene homopolymer, (A2) 47 wt% of propylene-ethylene copolymer, (B) 15 wt% of thermoplastic elastomer, (C) 20 wt% of inorganic filler, and (D2) The mixture was mixed to prepare a polypropylene resin composition, which was then extruded using a twin-screw extruder. The extruded pellets were mixed with 2% by weight of sodium hydrogen bicarbonate (E) as a foaming agent (E) and injection-molded using a core-back mold to prepare specimens.

The component ratios of the polypropylene resin composition and the foaming agent of Example 1 and Comparative Examples 1 to 4 were summarized in Table 1 below.

Example Comparative Example One One 2 3 4 (A) (A1) 15 15 15 15 15 (A2) 47 48 44 44 47 (B) 15 15 15 15 15 (C) 20 20 20 20 20 (D) (D1) One - 4 One - (D2) - - - - One (E) 2 2 2 5 2 Sum 100 100 100 100 100

(Unit: wt%)

≪ Property evaluation method &

The following items were measured to evaluate the physical properties and processability of the specimens produced according to Example 1 and Comparative Examples 1 to 4, and the results are shown in Table 2 below.

(1) Tensile strength (kgf / cm2): Measured according to ASTM D638.

(2) Elongation (%): Measured according to ASTM D638.

(3) IZOD impact strength (kgf · cm / cm): Measured according to ASTM D256 for a temperature condition of room temperature (23) at 1/4 notched condition.

(4) Flexural strength (kgf / cm2): Measured according to ASTM D790.

(5) Flexural modulus (kgf / cm 2): Measured according to ASTM D790.

(6) Specific gravity: Measured according to ASTM D792

(7) Injection appearance: The presence or absence of gas marks on the surface of the specimen was visually observed.

X: Gas mark generation

○: No gas mark

Example Comparative Example One One 2 3 4 The tensile strength
(kgf / cm2) 185 160 180 150 182 Elongation
(%) 40 37 40 20 38 Flexural strength
(kgf / cm2) 300 270 290 210 280 Flexural modulus
(kgf / cm2) 26,400 24,100 26,000 1,800 26,000 IZOD impact strength
(kgf · cm / cm) 8.9 8.7 3.5 2.0 8.5 importance 0.83 0.84 0.85 0.78 0.83 Injection Appearance ○ × ○ × ×

Referring to the results of Table 2, it can be seen that the specimen according to Example 1 exhibits excellent mechanical properties such as tensile strength, elongation, flexural strength, flexural modulus, impact strength and specific gravity. In addition, by containing 1 wt% of the nucleating agent (D), nucleation at the surface of the mold is sufficiently performed at the time of injection, and it can be confirmed that gas marks do not occur on the surface of the specimen.

On the other hand, the specimen of Comparative Example 1 produced by the polypropylene resin composition not containing the nucleating agent was not sufficiently nucleated at the mold surface at the time of injection, and the foaming gas was transferred to the surface, .

On the other hand, it can be confirmed that the impact strength of the specimen of Comparative Example 2 produced by the polypropylene resin composition containing more than 2% by weight of the core agent and 4% by weight of the core agent was decreased.

Also, it can be confirmed that the specimen of Comparative Example 3 produced by the polypropylene resin composition containing the blowing agent in an amount of more than 3% by weight and 5% by weight had a reduced mechanical strength due to excessive foaming gas.

In addition, in Comparative Example 4, it can be confirmed that nucleation was not sufficiently carried out, and a gas mark appeared on the appearance of the injection.

(A) 33 to 93% by weight of a polypropylene resin, (C) 1 to 30% by weight of an inorganic filler (B) 1 to 10% by weight of a thermoplastic elastomer, (D) 0.1 to 2% by weight of a nucleating agent and (E) 0.1 to 3% by weight of a foaming agent may be used as an interior material or an exterior material of a vehicle.

Fig. 1 is a view showing an example in which a molded article produced by a polypropylene resin composition is used as an exterior material of a vehicle, and Fig. 2 is an illustration showing an example in which a molded article produced by a polypropylene resin composition is used as an interior material of a vehicle.

1, the bumpers 10F, 10R of the vehicle 1 and the battery case 21 provided inside the bonnet 20 according to one embodiment are made of a polypropylene resin composition according to the above- As a material. In addition, the back panel molding can also be made from the polypropylene resin composition according to the above-described embodiment.

2, an interior material such as the instrument panel 30 and the door trim 40 of the vehicle 1 may also be a molded product made of a polypropylene resin composition according to the above-described embodiment.

However, the type of the interior material and the exterior material of the vehicle shown in Figs. 1 and 2 is merely an example in which the molded article manufactured by the polypropylene resin composition according to one embodiment can be applied, and the scope of the present invention is limited to this no.

Therefore, it goes without saying that the polypropylene resin composition according to one embodiment can also be used as a material for the interior and exterior materials other than the examples shown in FIGS. 1 and 2.

The vehicle interior and exterior materials manufactured by the polypropylene resin composition according to one embodiment can have excellent appearance in terms of light weight and mechanical properties and smooth surface.

The embodiments disclosed with reference to the accompanying drawings and tables have been described above. It will be understood by those of ordinary skill in the art that various changes in form and details may be made therein without departing from the spirit and scope of the present invention as defined by the following claims. The disclosed embodiments are illustrative and should not be construed as limiting.

1: vehicle
20: bonnet
30: Instrument panel
40: Door trim

Claims (21)

33 to 93% by weight, based on the total weight of the polypropylene resin composition, of a polypropylene resin;
1 to 30% by weight of a thermoplastic elastomer;
1 to 30% by weight of inorganic filler;
1 to 1.5% by weight of a sodium phosphate-based nucleating agent; And
0.1 to 3% by weight of a foaming agent,
In the polypropylene resin,
A propylene homopolymer contained in a proportion of 20 to 30% by weight based on the total weight of the polypropylene resin, and
Wherein the propylene-ethylene copolymer is contained in a proportion of 70 to 80% by weight based on the total weight of the polypropylene resin. delete delete delete The method according to claim 1,
The propylene homopolymer,
And a melt index (Melt Index) measured at 230 占 폚 under a load of 2.16 kg of 1 to 100 g / 10 min. The method according to claim 1,
The propylene-ethylene copolymer is a propylene-
A polypropylene resin composition having a melt index (Melt Index) of 1 to 100 g / 10 min as measured at 230 占 폚 under a load of 2.16 kg The method according to claim 1,
The thermoplastic elastomer is a thermoplastic elastomer,
An ethylene-alpha olefin copolymer having 4 or more carbon atoms, and a styrene-diene copolymer. 8. The method of claim 7,
The above-mentioned alpha-olefin copolymer of ethylene-
A polypropylene resin composition comprising at least one of an ethylene butene-1 copolymer (EBM) and an ethylene octene-1 copolymer (EOM). 8. The method of claim 7,
The above alpha-olefin copolymer having 4 or more carbon atoms is,
And 12 to 45% by weight based on the total weight of the thermoplastic elastomer. 8. The method of claim 7,
The above-mentioned styrene-diene-
Styrene-butylene-styrene block copolymer, styrene-ethylene-butylene-styrene block copolymer, styrene-isoprene-styrene block copolymer, styrene-ethylene-propylene block copolymer and styrene- ≪ RTI ID = 0.0 > polypropylene < / RTI > The method according to claim 1,
The thermoplastic elastomer is a thermoplastic elastomer,
A melt index of 10 to 40 g / 10 min as measured at 230 占 폚 under a load of 2.16 kg. The method according to claim 1,
The thermoplastic elastomer is a thermoplastic elastomer,
Wherein the polypropylene resin composition is contained in a proportion of 3 to 25% by weight based on the total weight of the polypropylene resin composition. The method according to claim 1,
The inorganic filler,
A fibrous inorganic filler, and a non-fibrous inorganic filler. 14. The method of claim 13,
The fiber-based inorganic filler may be,
And an average fiber length of 1 to 5 mm. 14. The method of claim 13,
The fiber-based inorganic filler may be,
Wherein the polypropylene resin composition comprises at least one of glass fiber, carbon fiber and metal fiber. 14. The method of claim 13,
Wherein the non-fibrous inorganic filler is a non-
Talc, calcium carbonate, barium sulfate, glass bubbles and glass beads. The method according to claim 1,
The sodium phosphate-
A polypropylene resin composition represented by the following formula (1).
[Chemical Formula 1]

R and R 'are each a hydrogen atom or a substituted or unsubstituted alkyl group, and Y is a substituent. 18. The method of claim 17,
The above-
A vinyl group, an amino group, a methacrylic group, an epoxy group, a mercapto group, a phenol group and a phenyl group. 18. A molded article produced by the polypropylene resin composition according to any one of claims 1 to 18. 20. The method of claim 19,
The blowing agent may contain,
0.5 to 1.5% by weight. 20. The method of claim 19,
The above-
The interior material of the vehicle and the exterior material of the vehicle.

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