KR20160123473A - Thermoplastic elastomer composition - Google Patents

Thermoplastic elastomer composition Download PDF

Info

Publication number
KR20160123473A
KR20160123473A KR1020150053422A KR20150053422A KR20160123473A KR 20160123473 A KR20160123473 A KR 20160123473A KR 1020150053422 A KR1020150053422 A KR 1020150053422A KR 20150053422 A KR20150053422 A KR 20150053422A KR 20160123473 A KR20160123473 A KR 20160123473A
Authority
KR
South Korea
Prior art keywords
thermoplastic elastomer
elastomer composition
weight
bio
parts
Prior art date
Application number
KR1020150053422A
Other languages
Korean (ko)
Inventor
이무정
이원희
홍경민
이상현
최재원
윤영기
전재욱
김영식
백승호
김기재
Original Assignee
(주) 화승소재
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by (주) 화승소재 filed Critical (주) 화승소재
Priority to KR1020150053422A priority Critical patent/KR20160123473A/en
Publication of KR20160123473A publication Critical patent/KR20160123473A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/16Elastomeric ethene-propene or ethene-propene-diene copolymers, e.g. EPR and EPDM rubbers
    • C08K3/0033
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/0008Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/0025Crosslinking or vulcanising agents; including accelerators
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/0008Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/005Stabilisers against oxidation, heat, light, ozone
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/06Polyethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/12Polypropene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2207/00Properties characterising the ingredient of the composition
    • C08L2207/04Thermoplastic elastomer

Abstract

The present invention relates to a resin composition comprising a matrix resin comprising one or both of Bio EPDM (Ethylene Propylene Diene Monomer) rubber and polypropylene and bio-polyethylene; Peroxide crosslinking agents; Crosslinking auxiliary; Antioxidants; Inorganic fillers; Polypropylene wax; And UV stabilizers. ≪ Desc / Clms Page number 2 >

Description

THERMOPLASTIC ELASTOMER COMPOSITION [0001]

The present invention relates to a thermoplastic elastomer composition using a biomaterial.

Rubber has a disadvantage in that it can not be used for recycling and productivity is low, and the need for replacement thereof has been greatly increased recently. A thermoplastic elastomer (TPE) has been developed as a material to solve the problem of such a rubber.

The thermoplastic elastomer is recognized as a recyclable rubber material between plastic and rubber, and has been used as a substitute for rubber in automobile parts. Recently, as the environment problem of PVC has emerged, it is more promising as a substitute material of soft PVC It is becoming.

Currently, it is actively promoting the use of biomaterials as a policy of national / corporations that encourages the use of various environmental regulations and environmentally friendly materials.

Korean Patent Laid-Open Publication No. 2005-0020003 (Mar. 4, 2005)

The present invention provides an eco-friendly thermoplastic elastomer composition capable of enhancing the bio-derived portion of the composition while maintaining physical properties equivalent to or superior to those of conventional petroleum-based PP / EPDM thermoplastic elastomers, do.

The present invention relates to a bio-EPDM (Ethylene Propylene Diene Monomer) rubber, and a matrix resin comprising one or both of polypropylene and bio-polyethylene; Peroxide crosslinking agents; Crosslinking auxiliary; Antioxidants; Inorganic fillers; Polypropylene wax; And UV (ultraviolet light) stabilizer, wherein the thermoplastic elastomer composition comprises:

The content of the bio EPDM rubber is 20 to 50% by weight based on the total weight of the thermoplastic elastomer composition,

The content of the peroxide crosslinking agent is 0.25 to 0.70 parts by weight based on 100 parts by weight of the matrix resin,

The content of the crosslinking aid is 0.1 to 0.5 parts by weight based on 100 parts by weight of the matrix resin,

The content of the antioxidant is 0.1 to 0.5 parts by weight based on 100 parts by weight of the matrix resin,

The content of the inorganic filler is 10 to 20 parts by weight based on 100 parts by weight of the matrix resin,

The content of the polypropylene wax is 0.5 to 1.0 part by weight based on 100 parts by weight of the matrix resin,

Wherein the content of the UV stabilizer is 0.5 to 10 parts by weight based on 100 parts by weight of the matrix resin.

The bio thermoplastic elastomer composition according to the present invention can be used as an environmentally friendly thermoplastic elastomer composition while replacing the petroleum EPDM with an existing eco-friendly thermoplastic elastomer by replacing the existing petroleum EPDM.

Hereinafter, the thermoplastic elastomer composition according to the present invention will be described in detail.

In the present invention, the bio EPDM rubber means an EPDM rubber derived from ethylene produced by using a biomaterial such as sugar cane, corn, soybean, and the like.

The thermoplastic elastomer composition according to the present invention contains the bio EPDM rubber in an amount of 20 to 50% by weight based on the total weight of the thermoplastic elastomer composition. When the content of the bio EPDM rubber is less than 20% by weight, If the content of the bio EPDM rubber exceeds 50% by weight, the viscosity of the product increases and the extrusion molding operation becomes difficult, and the production cost of the product increases.

In one embodiment of the present invention, the bio EPDM rubber has a Mooney viscosity of at least 55 at 125 占 폚.

In the present invention, the Mooney viscosity is measured through a Mooney viscometer. When the material to be measured is put into a die heated at a specific temperature and rotated, the torque value of a rotating spindle it means.

In one embodiment of the present invention, the bio EPDM rubber includes 5-ethylidene-2-norbornene (ENB).

In one embodiment of the present invention, the content of the 5-ethylidene-2-norbornene is 4 to 9% by weight based on the total weight of the bio EPDM rubber. If the content of the polypropylene is less than 4% by weight, there may be a problem in extrusion / injection molding. If the content of the polypropylene exceeds 9% by weight, the hardness and strength of the product may increase, and cutting during extrusion / injection molding may be difficult.

In a first embodiment of the present invention, the matrix resin comprises a thermoplastic elastomer composition wool characterized by comprising bio EPDM rubber and polypropylene.

In one aspect of the first aspect of the present invention, the content of the polypropylene is 30 to 40% by weight based on the total weight of the thermoplastic elastomer composition. If the content of the polypropylene is less than 30% by weight, there may be a problem in extrusion / injection molding. If the content of the polypropylene is more than 50% by weight, the hardness may increase and there may be a sensitivity problem of the product.

In one aspect of the first embodiment of the present invention, the polypropylene has a melt index (MI) of 0.2 to 0.5 at 230 占 폚 and 2.16 kg. If the melt index of the polypropylene is less than 0.2 at 230 캜 and at 2.16 kg, it is disadvantageous in extrusion / injection molding. If the melt index is higher than 0.5, control becomes difficult during extrusion / injection molding due to a decrease in viscosity.

In the second embodiment of the present invention, the matrix resin includes bio EPDM rubber and bio-polyethylene.

In the present invention, bio-polyethylene refers to polyethylene produced by using biomaterials such as sugar cane, corn, soybeans and the like.

In one aspect of the second aspect of the present invention, the content of the bio-polyethylene is 20 to 30% by weight based on the total weight of the thermoplastic elastomer composition. If the content of the bio-polyethylene is less than 20% by weight, there may be a problem in the extrusion / injection molding. If the content is more than 30% by weight, the hardness may increase and the product may have sensitivity problems.

In one aspect of the second embodiment of the present invention, the bio-polyethylene has a melt index (MI) of 0.2 to 0.5 at 190 占 폚 and 2.16 kg. If the melt index of the bio-polyethylene is less than 0.2 at 190 ° C and less than 0.2 at 2.16 kg, if the melt index of the bio-polyethylene exceeds 0.5, problems in control of flow during extrusion / May occur.

The thermoplastic elastomer composition according to the present invention contains a peroxide crosslinking agent in an amount of 0.25 to 0.70 part by weight based on 100 parts by weight of the matrix resin. When the content of the crosslinking agent is less than 0.25 part by weight, And when it is more than 0.70 part by weight, the polypropylene chain is severed by the peroxide crosslinking agent, resulting in an open cell.

In one embodiment of the present invention, the peroxide crosslinking agent has a half-life temperature of 170 DEG C and a molecular weight of 290 or more, preferably 2,5-dimethyl-2,5-di- (tertiarybutylperoxy) hexane 2,5-Dimethyl-2,5-di- (tert-butylperoxy) -hexane).

The thermoplastic elastomer composition according to the present invention contains a crosslinking aid in an amount of 0.1 to 0.5 parts by weight based on 100 parts by weight of the matrix resin. When the content of the crosslinking agent is less than 0.1 parts by weight, If the amount is more than 1 part by weight, cross-linking may cause fish eye on the surface of the product, which may cause problems in the appearance of the product.

In one embodiment of the present invention, the crosslinking assistant is N, N'-m-phenylenedimaleimide, 1,2-polybutadiene, or a mixture thereof.

The thermoplastic elastomer composition according to the present invention contains the antioxidant in an amount of 0.1 to 0.5 parts by weight based on 100 parts by weight of the matrix resin. When the content of the antioxidant is less than 0.1 parts by weight, the physical properties of the composition are deteriorated. There may be a problem of performance deterioration. If the amount is more than 0.5 part by weight, a problem may occur that a product is blooming.

In one embodiment of the present invention, the antioxidant has a melting point of 120 ° C or higher and a whiteness of 95% or higher, preferably tetrakis (3,5-di-tert-butyl-4-hydroxyphenyl) Tetrakis- (3-dodecylthiopropionate), or a mixture thereof. The term " tetrakis (3,5-di-tert-butylphenyl) propionate " have.

The thermoplastic elastomer composition according to the present invention contains an inorganic filler in an amount of 10 to 20 parts by weight based on 100 parts by weight of the matrix resin. If the content of the inorganic filler is less than 10 parts by weight, the material ratio increases and its role as a filler becomes insignificant If it exceeds 20 parts by weight, the specific gravity of the product increases, and the extrusion molding operation becomes difficult due to the increase of the hardness and the flowability of the inorganic filler.

In one embodiment of the present invention, the inorganic filler has a particle size of 10 mu m or less and a whiteness of 95% or more.

In one embodiment of the present invention, the inorganic filler is calcium carbonate.

The thermoplastic elastomer composition according to the present invention contains the polypropylene wax in an amount of 0.5 to 1.0 part by weight based on 100 parts by weight of the matrix resin. When the content of the polypropylene wax is less than 0.5 part by weight, the scratch resistance The improvement effect is insufficient and it is not effective in improving the abrasion resistance. When the amount is 1.0 part by weight or more, the polypropylene wax is transferred to the product surface of the finished product, which may cause problems in implementation of product characteristics. When the content of the polypropylene wax is 0.5 parts by weight or more and 1.0 parts by weight or less, the surface slip property of the finished product is improved and the abrasion resistance is increased.

In one embodiment of the present invention, the propylene-based wax has a specific gravity of 0.90 or less and a melting point of 160 ° C or more.

The thermoplastic elastomer composition according to the present invention contains 0.5 to 10 parts by weight of a UV stabilizer per 100 parts by weight of the matrix resin. When the content of the UV stabilizer is less than 0.5 parts by weight, surface whitening and micro cracks If the amount is more than 10 parts by weight, a UV stabilizer having a low molecular weight may be migrated to the surface, resulting in a problem of blooming in appearance of the product.

In one embodiment of the present invention, the UV stabilizer is a benzotriazole type UV absorber, an Oligomeric Hindered Amine Light Stabilizer type UV stabilizer, or a mixture thereof.

In the third embodiment of the present invention, the thermoplastic elastomer composition further comprises a process oil, and the process oil does not limit the process oil so far as it serves to improve the processability of the composition.

In one aspect of the third aspect of the present invention, the process oil is paraffin oil, and the thermoplastic elastomer composition contains the paraffin oil in an amount of 20 to 50 parts by weight based on 100 parts by weight of the matrix resin. If the content is less than 20 parts by weight, the flowability during extrusion molding is poor, which may cause defective molding and defective work. If the content is more than 50 parts by weight, the melt strength may be lowered.

In one aspect of the third embodiment of the present invention, the paraffin oil has a kinematic viscosity at 40 DEG C of 170 or more. When the kinematic viscosity of the paraffin oil is 170 or more, the melt strength may be lowered due to viscosity increase of the product.

Hereinafter, the configuration and effects of the present invention will be described in more detail with reference to examples. However, these examples are provided for illustrative purposes only in order to facilitate understanding of the present invention, and the scope and scope of the present invention are not limited by the following examples.

( Manufacturing example  One) EPDM  Thermoplastics including mattress resins composed of rubber and polypropylene Erastomeric  Produce

Constituent Comparative Example 1 Comparative Example 2 Comparative Example 3 Example 1 Example 2 Example 3 Petroleum-based EPDM rubber (% by weight) 60 70 80 - - - Bio EPDM rubber
(weight%)
- - - 60 70 80
Polypropylene (% by weight) 40 30 20 40 30 20 Peroxide crosslinking agent (parts by weight) 0.25 0.25 0.25 0.25 0.25 0.25 Crosslinking aid (parts by weight) 0.25 0.25 0.25 0.25 0.25 0.25 Antioxidant
(Parts by weight)
0.2 0.2 0.2 0.2 0.2 0.2
Inorganic filler
(Parts by weight)
10 10 10 10 10 10
UV stabilizer
(Parts by weight)
5 5 5 5 5 5
Polypropylene wax
(Parts by weight)
One One One One One One
Highly viscous paraffin oil
(Parts by weight)
40 40 40 40 40 40

In Table 1, the weight% is a content ratio of the thermoplastic elastomer composition to the total weight, and the weight ratio is a content ratio with respect to 100 weight ratio of the matrix resin comprising petroleum-based or bio EPDM rubber and polypropylene.

In Table 1, trade names and manufacturers of each component are as follows.

Petroleum-based EPDM rubber: [KEP-2480, KEP Corporation]

Bio-based EPDM rubber: [KELTAN 5470,9950 ECO, LANXESS]

General-Purpose Polypropylene: [RP2400, Korean Oil Company]

Peroxide crosslinking agent: 2,5-dimethyl-2,5-di- (tertiarybutylperoxy) hexane [Luperox 101-50D, Atochem]

Crosslinking aid: N, N'-m-phenylene dimaleimide [TAC-50, DEGUSA]

Antioxidant: tetrakis (3,5-di-tertiary-butyl-4-hydroxyphenyl) propionate [SEENOX 412, Shipro Kasei]

Inorganic filler: calcium carbonate [SF, Dongho Calcium]

Polypropylene wax: [500 series, Lion Chemtech]

UV stabilizer: Benzotriazole type UV absorber, Oligomeric HALS type UV stabilizer [BASF]

Paraffin oil: [KL900B, SJC]

The thermoplastic elastomer compositions of Comparative Examples 1 to 3 and Examples 1 to 3 in the composition as shown in Table 1 were prepared by an extrusion molding method according to a general manufacturing method known in the art.

( Experimental Example  One) Comparative Example  1 to 3 and Example  1 to 3 < / RTI > Erastomeric  Basic property measurement

The basic properties of the thermoplastic elastomers of Comparative Examples 1 to 3 and Examples 1 to 3 prepared in Preparation Example 1 were measured according to KS M 6518, and the hardness and tensile specimen [dumbbell triangle], tear specimen [Tear A type] was used. The measurement results are shown in Table 2 below.

division Comparative Example 1 Comparative Example 2 Comparative Example 3 Example 1 Example 2 Example 3 basic
Properties
Hardness (Shore A) 90 88 86 90 88 86
Tensile strength (kgf / cm3) 180 170 160 180 170 160 Elongation at break (%) 680 660 640 680 660 640 Tear strength (kgf / cm) 72 60 54 70 61 53

As shown in Table 2 above, when the bio EPDM rubber other than the petroleum EPDM rubber was included as the mattress resin in Examples 1 to 3, the physical properties of the EPDM rubber with the existing thermoplastic elastomer compositions as in Comparative Examples 1 to 3 were equivalent . ≪ / RTI > Therefore, compared to the conventional thermoplastic elastomer compositions as in Comparative Examples 1 to 3, the bio-derived portion in the thermoplastic elastomer can be increased to highlight the environment-friendly aspect.

( Manufacturing example  2) polypropylene, bio-polyethylene, or mixtures thereof and EPDM  Thermoplastics including mattress resins made of rubber Erastomer  Preparation of composition

The thermoplastic elastomer compositions of Comparative Examples 1, 4 and 5 and Examples 1, 4 and 5 were prepared in the same manner as in Production Example 1, respectively, with the compositions shown in Table 3 below.

Constituent Comparative Example 1 Comparative Example 4 Comparative Example 5 Example 1 Example 4 Example 5 Petroleum-based EPDM rubber (% by weight) 60 60 60 - - - Bio EPDM rubber
(weight%)
- - - 60 60 60
Polypropylene (% by weight) 40 20 - 40 20 - Bio-polyethylene (% by weight) - 20 40 - 20 40 Crosslinking agent (parts by weight) 0.25 0.25 0.25 0.25 0.25 0.25 Crosslinking aid (parts by weight) 0.25 0.25 0.25 0.25 0.25 0.25 Antioxidant
(Parts by weight)
0.2 0.2 0.2 0.2 0.2 0.2
Inorganic filler
(Parts by weight)
10 10 10 10 10 10
UV stabilizer
(Parts by weight)
5 5 5 5 5 5
Polypropylene wax
(Parts by weight)
One One One One One One
Highly viscous paraffin oil
(Parts by weight)
40 40 40 40 40 40

In Table 3, the weight% of the constituent components is the content ratio of the thermoplastic elastomer composition with respect to the total weight, and the weight ratio of the thermoplastic elastomer composition to the thermoplastic elastomer composition is in a weight ratio of 100 to the weight ratio of the mattress resin composed of petroleum or polypropylene, .

In Table 3, the trade name of the bio-polyethylene and its manufacturer are [SGM9450F, EcoMax Korea Co., Ltd.], and the trade names and manufacturers of the remaining components are shown in Table 1.

( Experimental Example  2) Comparative Example  1, 4, 5, Example  1, 4, and 5, Erastomeric  Basic property measurement

The basic properties of the thermoplastic elastomers of Comparative Examples 1, 4, 5 and Examples 1, 4 and 5 prepared in Preparation Example 2 were measured according to KS M 6518, and the hardness and tensile specimen ] And tear specimen [Tear A type] were used. The measurement results are shown in Table 4 below.

division Comparative Example 1 Comparative Example 4 Comparative Example 5 Example 1 Example 4 Example 5 basic
Properties
Hardness (Shore A) 90 87 84 90 85 81
Tensile strength (kgf / cm3) 180 170 160 180 163 150 Elongation at break (%) 680 670 650 680 660 630 Tear strength (kgf / cm) 70 67 62 70 64 55

As shown in Table 4, when the content of bio-polyethylene was increased in Example 5, the physical properties due to the compatibility problem were partially reduced, but the hardness, tensile strength, elongation at break and tear strength were not significantly decreased , It can be seen that when the polypropylene and bio-polyethylene are used in appropriate combination as in Example 4, the physical properties and the physical properties with the existing thermoplastic elastomer composition are equivalent. Thus, in comparison with conventional thermoplastic elastomer compositions such as Comparative Examples 1, 4, and 5, the thermoplastic elastomer composition includes the bio EPDM rubber, and the content of bio-polyethylene is increased to increase the bio-derived portion in the thermoplastic elastomer The environmentally friendly aspect can be highlighted.

Claims (16)

A bio-EPDM (Ethylene Propylene Diene Monomer) rubber, and a matrix resin comprising one or both of polypropylene and bio-polyethylene; Peroxide crosslinking agents; Crosslinking auxiliary; Antioxidants; Inorganic fillers; Polypropylene wax; And a UV stabilizer, wherein the thermoplastic elastomer composition comprises:
The content of the bio EPDM rubber is 20 to 50% by weight based on the total weight of the thermoplastic elastomer composition,
The content of the peroxide crosslinking agent is 0.25 to 0.70 parts by weight based on 100 parts by weight of the matrix resin,
The content of the crosslinking aid is 0.1 to 0.5 parts by weight based on 100 parts by weight of the matrix resin,
The content of the antioxidant is 0.1 to 0.5 parts by weight based on 100 parts by weight of the matrix resin,
The content of the inorganic filler is 10 to 20 parts by weight based on 100 parts by weight of the matrix resin,
The content of the polypropylene wax is 0.5 to 1.0 part by weight based on 100 parts by weight of the matrix resin,
Wherein the content of the UV stabilizer is 0.5 to 10 parts by weight based on 100 parts by weight of the matrix resin.
The bio EPDM rubber according to claim 1, wherein the bio EPDM rubber has a Mooney viscosity of at least 55 at 125 ° C, the bio EPDM rubber comprises 5-ethylidene-2-norbornene, Wherein the content of the thermoplastic elastomer composition is 4 to 9% by weight based on the total weight of the bio EPDM rubber. The thermoplastic elastomer composition according to claim 1, wherein the matrix resin comprises bio EPDM rubber and polypropylene. The thermoplastic elastomer composition according to claim 3, wherein the polypropylene content is 30 to 40% by weight based on the total weight of the thermoplastic elastomer composition. The thermoplastic elastomer composition according to claim 1, wherein the polypropylene has a melt index (MI) of from 0.2 to 0.5 at 230 DEG C and 2.16 kg. The thermoplastic elastomer composition according to claim 1, wherein the matrix resin comprises bio EPDM rubber and bio-polyethylene. The thermoplastic elastomer composition according to claim 6, wherein the content of the bio-polyethylene is 20 to 30% by weight based on the total weight of the thermoplastic elastomer composition. The thermoplastic elastomer composition according to claim 1, wherein the bio-polyethylene has a melt index (MI) of 190 ° C or 2.16 kg at 0.2 to 0.5. The thermoplastic elastomer composition according to claim 1, wherein the peroxide crosslinking agent has a half-life temperature of 170 ° C and a molecular weight of 290 or more. The thermoplastic elastomer composition according to claim 1, wherein the antioxidant has a melting point of 120 ° C or higher and a whiteness of 95% or higher. The thermoplastic elastomer composition according to claim 1, wherein the inorganic filler has a particle size of 10 탆 or less and a whiteness of 95% or more. The thermoplastic elastomer composition according to claim 1, wherein the inorganic filler is calcium carbonate. The thermoplastic elastomer composition according to claim 1, wherein the polypropylene wax has a specific gravity of 0.90 or less and a melting point of 160 ° C or more. The thermoplastic elastomer composition according to claim 1, wherein the UV stabilizer is a benzotriazole type UV absorber, a HALS type UV stabilizer (Oligomeric Hindered Amine Light Stabilizer type UV stabilizer), or a mixture thereof. Composition. The thermoplastic elastomer composition of claim 1, wherein the thermoplastic elastomer composition further comprises a paraffin oil. 16. The thermoplastic elastomer composition according to claim 15, wherein the paraffin oil has a kinematic viscosity at 40 DEG C of 170 or more.
KR1020150053422A 2015-04-15 2015-04-15 Thermoplastic elastomer composition KR20160123473A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1020150053422A KR20160123473A (en) 2015-04-15 2015-04-15 Thermoplastic elastomer composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1020150053422A KR20160123473A (en) 2015-04-15 2015-04-15 Thermoplastic elastomer composition

Related Child Applications (1)

Application Number Title Priority Date Filing Date
KR1020170077079A Division KR102006842B1 (en) 2017-06-19 2017-06-19 Thermoplastic elastomer composition using bio-based material

Publications (1)

Publication Number Publication Date
KR20160123473A true KR20160123473A (en) 2016-10-26

Family

ID=57251461

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1020150053422A KR20160123473A (en) 2015-04-15 2015-04-15 Thermoplastic elastomer composition

Country Status (1)

Country Link
KR (1) KR20160123473A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3879155A1 (en) * 2020-03-09 2021-09-15 ContiTech USA, Inc. Sustainable industrial hose
KR102361628B1 (en) * 2020-11-12 2022-02-14 한국신발피혁연구원 Bio epdm foam composition for ocean suit
US11565494B2 (en) 2020-03-09 2023-01-31 Contitech Usa, Inc. Sustainable industrial hose

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20050020003A (en) 2003-08-20 2005-03-04 에스케이 주식회사 Thermoplastic elastomer composition and Method for preparing the same

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20050020003A (en) 2003-08-20 2005-03-04 에스케이 주식회사 Thermoplastic elastomer composition and Method for preparing the same

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3879155A1 (en) * 2020-03-09 2021-09-15 ContiTech USA, Inc. Sustainable industrial hose
US11168815B2 (en) 2020-03-09 2021-11-09 Contitech Usa, Inc. Sustainable industrial hose
US11565494B2 (en) 2020-03-09 2023-01-31 Contitech Usa, Inc. Sustainable industrial hose
US11867324B2 (en) 2020-03-09 2024-01-09 Contitech Usa, Inc. Sustainable industrial hose
KR102361628B1 (en) * 2020-11-12 2022-02-14 한국신발피혁연구원 Bio epdm foam composition for ocean suit

Similar Documents

Publication Publication Date Title
KR102006842B1 (en) Thermoplastic elastomer composition using bio-based material
KR101779365B1 (en) Chloroprene rubber composition, and vulcanizate and molding thereof
CA1333308C (en) Olefinic thermoplastic elastomer composition
KR101155869B1 (en) Thermo-reversible Crosslinked elastomer and Method producing thereof
KR101811191B1 (en) Chloroprene rubber composition, and vulcanizates and moldings thereof
KR101270545B1 (en) Supramolecular network thermo-reversible crosslinked elastomer having high mechanical properties and low compression set and Method producing thereof
CN104530542B (en) Halogen-free aging-resistant strippable shielding material for rubber sleeve cable
CN1861390B (en) Laminated product and process for producing the same
KR101836638B1 (en) EPDM based rubber composition for sponge section in weather strip of passenger car
EP1300620B1 (en) Hose made of thermoplastic elastomer
DE102016103822A1 (en) A thermoplastic elastomer composition of an elastomer, a non-elastomeric polyolefin and a thermoplastic polyolefin block copolymer-based elastomer
KR20160123473A (en) Thermoplastic elastomer composition
WO1990006859A1 (en) Air impermeable containers
DE602004012505T2 (en) Rubber hose material
DE102013002595A1 (en) Process for the preparation of a thermoplastic elastomer composition and process for the preparation of a composite article
CN107828121A (en) A kind of dynamic vulcanization thermoplastic elastomer material and preparation method thereof
KR960007010B1 (en) Two-layer sheets of thermoplastic elastomers
DE69932976T2 (en) Resin compositions for surface layers and laminates thereof
JP6040283B1 (en) Protective member for cable connection and cable connection
JP5189245B2 (en) Thermoplastic elastomer composition and molded article thereof
KR102142118B1 (en) Ionomer supramolecular network thermo-reversible crosslinked elastomer having high mechanical properties and low compression set and Producing method of dynamic crosslinked thermoplastic elastomer using the same
KR101154879B1 (en) Thermoplastic elastomer composition for guard valve body
KR20170046897A (en) Supramolecular network thermo-reversible crosslinked elastomer having high mechanical properties and low compression set and Method producing thereof
KR100466384B1 (en) Thermoplastic elastomer composition for shock absorbing
JP4922820B2 (en) Composite member and manufacturing method thereof

Legal Events

Date Code Title Description
A201 Request for examination
AMND Amendment
E902 Notification of reason for refusal
AMND Amendment
AMND Amendment
A107 Divisional application of patent