KR100214247B1 - Thermoplastic resin composition - Google Patents

Thermoplastic resin composition Download PDF

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KR100214247B1
KR100214247B1 KR1019960045725A KR19960045725A KR100214247B1 KR 100214247 B1 KR100214247 B1 KR 100214247B1 KR 1019960045725 A KR1019960045725 A KR 1019960045725A KR 19960045725 A KR19960045725 A KR 19960045725A KR 100214247 B1 KR100214247 B1 KR 100214247B1
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thermoplastic resin
resin composition
antioxidant
weight
resistance
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KR19980027067A (en
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이병진
강정원
허철호
김형준
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김윤
주식회사삼양사
정몽규
현대자동차주식회사
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L69/00Compositions of polycarbonates; Compositions of derivatives of polycarbonates
    • 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
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/13Phenols; Phenolates
    • 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
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3472Five-membered rings
    • C08K5/3475Five-membered rings condensed with carbocyclic rings
    • 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
    • C08K5/36Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/41Compounds containing sulfur bound to oxygen
    • C08K5/42Sulfonic acids; Derivatives thereof
    • 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
    • C08K5/49Phosphorus-containing compounds
    • C08K5/51Phosphorus bound to oxygen
    • C08K5/52Phosphorus bound to oxygen only
    • C08K5/524Esters of phosphorous acids, e.g. of H3PO3
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L55/00Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
    • C08L55/02ABS [Acrylonitrile-Butadiene-Styrene] polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • C08L2666/24Graft or block copolymers according to groups C08L51/00, C08L53/00 or C08L55/02; Derivatives thereof

Abstract

본 발명은 열가소성 수지 조성물에 관한 것으로서, 더욱 상세하게는 폴리카보네이트 수지와 아크릴로니트릴-부타디엔-스티렌 공중합체를 주성분으로 하는 열가소성 수지 조성물에 있어서 통상의 상용화제를 첨가하지 않고 상기 수지만을 사용하고 최적의 자외선안정제와 산화방지제를 조합하여 첨가함으로써 내열성, 내충격성, 내열노화성 및 내광노화성이 우수한 열가소성 수지 조성물에 관한 것이다.The present invention relates to a thermoplastic resin composition, and more particularly, to a thermoplastic resin composition comprising a polycarbonate resin and an acrylonitrile-butadiene-styrene copolymer as a main component without using a conventional compatibilizer, The present invention relates to a thermoplastic resin composition excellent in heat resistance, impact resistance, heat aging resistance and photo-aging resistance by adding an ultraviolet stabilizer and an antioxidant in combination.

Description

열가소성 수지 조성물Thermoplastic resin composition

본 발명은 열가소성 수지 조성물에 관한 것으로서, 더욱 상세하게는 폴리카보네이트 수지와 아크릴로니트릴-부타디엔-스티렌 공중합체를 주성분으로 하는 열가소성 수지 조성물에 있어서 통상의 상용화제를 첨가하지 않고 상기 수지만을 사용하고 최적의 자외선안정제와 산화방지제를 조합하여 첨가함으로써 내열성, 내충격성, 내열노화성 및 내광노화성이 우수한 열가소성 수지 조성물에 관한 것이다.The present invention relates to a thermoplastic resin composition, and more particularly, to a thermoplastic resin composition comprising a polycarbonate resin and an acrylonitrile-butadiene-styrene copolymer as a main component without using a conventional compatibilizer, The present invention relates to a thermoplastic resin composition excellent in heat resistance, impact resistance, heat aging resistance and photo-aging resistance by adding an ultraviolet stabilizer and an antioxidant in combination.

자동차의 내장재로 쓰이는 인스트루먼트 패널(instrument panel)은 운전자의 앞쪽에 위치하여 자동차의 엔진룸과 운전석을 분리시켜 주며, 또한 각종 계기판이 부착되어지는 장치로써 엔진룸의 고열을 차단시켜 주고 충돌시 운전자를 보호하여 주어야 하기 때문에 높은 내열성과 내충격성이 요구된다.The instrument panel, which is used as an interior material for automobiles, is located in front of the driver and separates the engine room and the driver's seat of the car. It also has various instrument panels attached to it to block the high temperature of the engine room. High heat resistance and impact resistance are required.

또한, 여름에는 자동차의 실내온도가 90 ℃ 이상으로 올라가고 한겨울에는 자동차의 실내온도가 -10 ℃ 이하로 내려가기 때문에 내열노화성 및 내한성을 동시에 가져야하며, 차내로 들어오는 자외선에 강한 내광노화성을 가져야 한다.Also, in summer, the indoor temperature of a car rises to 90 ° C or higher, and in the middle of winter, the temperature of a car falls down to -10 ° C or lower. Therefore, it must have heat aging resistance and cold resistance. do.

이와같은 물성을 만족시키기 위해 높은 내열성과 내한성을 가지는 폴리카보네이트수지와 아크릴로니트릴-부타디엔-스티렌 수지를 주성분으로 하는 수지 조성물이 사용되고 있으나, 이들은 내열노화성 및 내광노화성을 만족시키지 못하는 문제가 있다.In order to satisfy such physical properties, a resin composition containing a polycarbonate resin having high heat resistance and cold resistance and an acrylonitrile-butadiene-styrene resin as a main component has been used, but these resins have problems in that they can not satisfy the heat aging resistance and the photo-aging resistance .

폴리카보네이트 수지는 내충격성, 전기적 특성, 치수안정성 및 투명성이 우수하여 각종 성형물, 필름, 엔지니어링 플라스틱 등의 용도로 광범위하게 사용되고 있지만, 수지 자체의 용융점도가 높아 성형성이 불량하고 충격강도의 두께의존성 및 내용제성이 약한 단점이 있다.The polycarbonate resin is widely used for various molded products, films, engineering plastics and the like because of its excellent impact resistance, electrical properties, dimensional stability and transparency. However, since the resin itself has a high melt viscosity, the moldability is poor, And a weak solvent resistance.

이를 개선하기 위하여 폴리카보네이트 수지와 아크릴로니트릴-부타디엔-스티렌 수지를 블렌드시킴으로써 기계적 성질, 가공성 및 내용제성이 우수한 수지를 얻을 수 있게 되어 많은 제품의 성형소재로 사용될 수 있게 되었다.By blending polycarbonate resin and acrylonitrile-butadiene-styrene resin, it is possible to obtain a resin having excellent mechanical properties, processability and solvent resistance, so that it can be used as a molding material for many products.

그러나, 폴리카보네이트 수지와 아크릴로니트릴-부타디엔-스티렌 수지를 블렌드시킨 조성물은 충격강도의 두께의존성이나 성형가공성은 다소 개선되었지만 아크릴로니트릴-부타디엔-스티렌 수지의 내열성으로 인한 내열성의 문제점과 아크릴로니트릴-부타디엔-스티렌 수지내에 포함된 부타디엔 고무로 인해 내열노화성의 문제는 여전히 남게되어 이를 해결하기 위한 연구가 활발히 진행되고 있다.However, although the composition in which the polycarbonate resin and the acrylonitrile-butadiene-styrene resin are blended has a somewhat improved thickness dependency of the impact strength and molding processability, there is a problem of heat resistance due to the heat resistance of the acrylonitrile-butadiene- -Butadiene-styrene resin, the problem of heat aging resistance still remains, and studies for solving the problem have been actively conducted.

그 한예로서 일본특허공개 소 61-174257 호에서는 폴리카보네이트 수지와 아크릴로니트릴-부타디엔 수지의 혼합물에 α-올레핀 공중합체를 첨가하여 내열성을 향상시키고자 하였지만, 내열노화성 및 내충격성이 떨어지는 문제가 있다.As an example, Japanese Patent Application Laid-Open No. 61-174257 has attempted to improve the heat resistance by adding an? -Olefin copolymer to a mixture of a polycarbonate resin and an acrylonitrile-butadiene resin, but the problem of deterioration in heat aging resistance and impact resistance have.

또한, 일본특허공개 소 62-156850 호 및 대한민국특허 공개 제 95-792 호 및 제 94-18435 호 등에서는 상용화제 등을 첨가하여 내충격성을 향상시켰으나, 내열성 및 내열노화성은 우수하지 못한 문제가 있다.In addition, Japanese Patent Application Laid-Open No. 62-156850 and Korean Patent Laid-Open Nos. 95-792 and 94-18435 and the like have improved the impact resistance by adding a compatibilizing agent and the like, but the heat resistance and the heat aging resistance are not excellent .

본 발명자들은 상기와 같은 종래의 폴리카보네이트 수지와 아크릴로니트릴-부타디엔-스티렌 수지를 주성분으로 하는 인스트루먼트 패널용 열가소성 수지의 문제점을 해결하기 위하여 연구노력한 결과, 상용화제의 첨가없이 최적의 자외선안정제와 티오에스테르계, 포스파이트계 및 폐놀계 산화방지제를 조합하여 첨가한 결과 내열성, 내충격성, 내광노화성 및 내열노화성이 우수함을 알게되어 본 발명을 완성하였다.The inventors of the present invention have made efforts to solve the problems of the conventional polycarbonate resin and the thermoplastic resin for an instrument panel comprising an acrylonitrile-butadiene-styrene resin as a main component. As a result, it has been found that an ultraviolet stabilizer, Ester type, phosphite type, and phenolic type antioxidant, it was found that heat resistance, impact resistance, photo-aging resistance and heat aging resistance are excellent, and thus the present invention has been completed.

본 발명은 내열성, 내충격성, 내광노화성 및 내열노화성이 우수하여 자동차의 인스트루먼트 패널재로서 적합한 열가소성 수지 조성물을 제공하는 데 그 목적이 있다.An object of the present invention is to provide a thermoplastic resin composition which is excellent in heat resistance, impact resistance, photo-aging resistance and heat aging resistance, and which is suitable as an instrument panel material for automobiles.

본 발명은 폴리카보네이트 수지와 아크릴로니트릴-부타디엔-스티렌 수지를 주성분으로 하는 열가소성 수지 조성물에 있어서, 상기 수지 100 중량부에 대하여 벤조트리아졸계 자외선안정제 0.3∼0.5 중량부, 티오에스테르계 산화방지제와 포스파이트계 산화방지제 0.8∼1.2 중량부 및 페놀계 산화방지제 0.4∼0.6 중량부를 첨가하여 이루어진 것을 그 특징으로 한다.The present invention relates to a thermoplastic resin composition comprising a polycarbonate resin and an acrylonitrile-butadiene-styrene resin as main components, wherein 0.3 to 0.5 parts by weight of a benzotriazole-based ultraviolet stabilizer is added to 100 parts by weight of the resin, 0.8 to 1.2 parts by weight of a pigment-based antioxidant and 0.4 to 0.6 parts by weight of a phenol-based antioxidant.

또한, 상기 티오에스테르계 산화방지제 함량(X)과 포스파이트계 산화방지제 함량(Y) 및 페놀계 산화방지제 함량(Z)은 다음 수식을 만족시키는 것을 그 특징으로 한다.The thioester-based antioxidant content (X), the phosphite-based antioxidant content (Y) and the phenol-based antioxidant content (Z) satisfy the following expressions.

X + Y ≥ 2Z 이고, X ≥ 2YX + Y? 2Z, and X? 2Y

이와같은 본 발명을 더욱 상세하게 설명하면 다음과 같다.Hereinafter, the present invention will be described in detail.

본 발명은 폴리카보네이트 수지와 아크릴로니트릴-부타디엔-스티렌 수지로 이루어진 열가소성 수지 조성물에 벤조트리아졸계 화합물을 자외선안정제로 첨가함으로써 내열성, 내충격성 및 내열노화성이 우수한 열가소성 수지 조성물에 관한 것이다.The present invention relates to a thermoplastic resin composition excellent in heat resistance, impact resistance and heat aging resistance by adding a benzotriazole-based compound as a UV stabilizer to a thermoplastic resin composition comprising a polycarbonate resin and an acrylonitrile-butadiene-styrene resin.

본 발명에서 사용되는 폴리카보네이트 수지는 수지 성분중 60∼80 중량%로 함유하는 바, 그 함량이 수지 성분중 60 중량% 미만이면 내열성이 저하되고 80 중량%를 초과하면 가공성이 좋지 않게 되어 성형시 미성형품이 발생하는 등의 문제가 있다. 그리고, 상기 폴리카보네이트 수지는 점도분자량이 23,000∼27,000인 범위의 것을 사용하는 바, 만일 그 점도분자량이 23,000 미만일 경우 기계적 물성이 낮아지고 27,000을 초과하는 경우 용융점도가 높아 성형시 문제가 발생한다. 여기서, 점도분자량이란 점도계를 이용하여 메틸렌클로라이드(Methylenchloride)를 용매로 하는 극한점도(η)를 구하여 H.Shell의 점도식 [η]=1.23 × 10-5M0.83에 의하여 얻어진 것을 의미한다.The polycarbonate resin used in the present invention is contained in an amount of 60 to 80% by weight of the resin component. When the content of the polycarbonate resin is less than 60% by weight, the heat resistance is deteriorated. When the content is more than 80% by weight, There is a problem that a molded article occurs. If the viscosity of the polycarbonate resin is in the range of 23,000 to 27,000, if the molecular weight of the polycarbonate resin is less than 23,000, the mechanical properties of the polycarbonate resin are lowered. If the viscosity exceeds 27,000, the polycarbonate resin has a high melt viscosity. Here, the viscosity molecular weight means the viscosity obtained by obtaining the intrinsic viscosity (?) Using a viscometer using methylenechloride as a solvent and by the viscosity formula [?] = 1.23 x 10 -5 M 0.83 of H.Shell.

한편, 본 발명에서 사용되는 아크릴로니트릴-부타디엔-스티렌 수지는 수지 성분중 20∼40 중량%로 함유하는 바, 그 함량이 20 중량% 미만이면 가공성이 나빠지고 40 중량%를 초과하면 내열성 및 내열노화성이 나빠진다. 그리고, 아크릴로니트릴-부타디엔-스티렌 수지 중의 부타디엔 고무 함량이 6∼16 중량%인 것이 바람직한 바, 부타디엔 고무의 함량이 6 중량% 미만이면 내충격성이 나빠지고 16 중량%를 초과하면 성형가공성 및 내열성이 떨어지는 문제가 있다.On the other hand, the acrylonitrile-butadiene-styrene resin used in the present invention contains 20 to 40% by weight of the resin component. When the content is less than 20% by weight, workability deteriorates. When the content exceeds 40% by weight, Aging deteriorates. The butadiene rubber content in the acrylonitrile-butadiene-styrene resin is preferably 6 to 16% by weight. When the butadiene rubber content is less than 6% by weight, the impact resistance is deteriorated. When the content is more than 16% by weight, There is a falling problem.

또한, 본 발명에서는 자외선안정제로서 벤조트리아졸계 화합물을 상기 수지 성분 100 중량부에 대하여 0.3∼0.5 중량부로 함유하는 바, 만일 그 함량이 0.3 중량부 미만이면 첨가효과가 미미하며 0.5 중량부를 초과하면 첨가효과가 상승되지 않고 오히려 다른 물성, 특히 내충격성을 떨어뜨리는 문제가 있다.In the present invention, the benzotriazole-based compound is contained in an amount of 0.3 to 0.5 parts by weight based on 100 parts by weight of the resin component. If the amount is less than 0.3 part by weight, the effect of addition is insignificant. There is a problem that the effect is not increased but rather the other properties, particularly the impact resistance, are lowered.

상기 벤조트리아졸계 자외선안정제로는 2-(2-히드록시-5-t-옥틸페닐)-벤조트리아졸 및 2-(5-메틸-2-히드록시-페닐)-벤조트리아졸 중에서 선택하여 1 종 이상의 것을 사용한다.The benzotriazole-based ultraviolet stabilizer may be selected from 2- (2-hydroxy-5- t -octylphenyl) -benzotriazole and 2- (5-methyl-2-hydroxy- Use more than species.

그리고, 산화방지제는 전체 상기 수지 성분 100 중량부에 대하여 1.2∼1.8 중량부로 함유하는 바, 이들의 구체적인 화합물로는 티오에스테르계(Thioester, X) 및 포스파이트(Phosphite, Y)계가 0.8∼1.2 중량부, 페놀계(Phenol, Z)가 0.4∼0.6 중량부로 함유되는 것이 바람직하다.The antioxidant is contained in an amount of 1.2 to 1.8 parts by weight based on 100 parts by weight of the whole resin component. Specific examples of the antioxidant include thioester (X) and phosphite (Y) (Phenol, Z) is contained in an amount of 0.4 to 0.6 parts by weight.

단, X + Y ≥ 2Z 이고, X ≥ 2Y가 되어야 한다.Provided that X + Y? 2Z and X? 2Y.

만일 전체 산화방지제의 함량이 상기 수지 성분 100 중량부에 대하여 1.2 중량부 미만이면 첨가효과가 미미하고, 1.8 중량부를 초과하면 첨가효과의 상승없이 기타물성이 떨어지게 된다.If the total amount of the antioxidant is less than 1.2 parts by weight based on 100 parts by weight of the resin component, the addition effect is insignificant. If the total antioxidant is more than 1.8 parts by weight, other properties are deteriorated without increasing the effect.

또한, X + Y가 Z의 2배보다 작거나 X가 Y의 2배보다 크지 않으면 초기의 열안정성에는 문제가 없으나, 내열노화성이 떨어져 장기 물성에 영향을 주게 된다.If X + Y is smaller than 2 times of Z or X is not larger than 2 times of Y, there is no problem in the initial thermal stability, but the thermal aging property is deteriorated and the long-term properties are affected.

여기서, 티오에스테르계 산화방지제로는 4,4'-디티오-비스(6-t-부틸-3-메틸페놀), 디스테아릴티오 디프로피오네이트 및 디미리스틸티오 디프로피오네이트 등이 있으며, 포스파이트계 산화방지제로는 트리스(2,4-디-t-부틸페닐)-포스파이트 및 비스(2,4-디-t-부틸)펜타에리스리톨-디포스파이트 등이 있다. 그리고, 페놀계 산화방지제로는 옥타데실-3-(3,5-디-t-부틸-4-히드록시페닐)-프로피오네이트, 옥타데실 2,5-디-t-부틸-4-히드록시히드로신나메이트 및 2,5-디-t-부틸-4-sec-부틸페놀 등이 있다.Examples of the thioester antioxidant include 4,4'-dithio-bis (6-t-butyl-3-methylphenol), distearyl thiodipropionate and dimyristyl thiodipropionate Tris (2,4-di- t -butylphenyl) -phosphite and bis (2,4-di- t -butyl) pentaerythritol-diphosphite. Then, the phenolic antioxidants are octadecyl-3- (3,5-di -t- butyl-4-hydroxyphenyl) -propionate, octadecyl-2,5-di-t-butyl-4-hydroxy Butylhydrocinnamate and 2,5-di- t -butyl-4-sec-butylphenol.

또한, 상기의 수지 조성물에 이형효과를 주기 위하여 이형제 및 조색품을 위한 조색제를 첨가할 수도 있다.In order to impart a releasing effect to the resin composition, a releasing agent and a coloring agent for the coloring product may be added.

상기한 바와 같은 본 발명에 따른 열가소성 수지 조성물은 종래의 열가소성 수지 조성물에 비하여 내충격성, 내열성, 내열노화성 및 내광노화성이 우수하여 자동차의 인스트루먼트 패널(instrument panel)부품으로 유용하게 사용될 수 있다.The thermoplastic resin composition according to the present invention as described above is superior in impact resistance, heat resistance, heat aging resistance and photo-aging resistance to conventional thermoplastic resin compositions and can be usefully used as instrument panel parts in automobiles.

이하, 본 발명을 실시예에 의거하여 상세히 설명하면 다음과 같은 바, 본 발명이 실시예에 의해 한정되는 것은 아니다.Hereinafter, the present invention will be described in more detail with reference to the following examples, but it should be understood that the invention is not construed as being limited thereto.

[실시예 1~3 및 비교예 1~4][Examples 1 to 3 and Comparative Examples 1 to 4]

다음 표에 나타낸 바와 같은 함량 및 조성으로 용융혼련용 압출기로 압출혼련하여 펠렛을 제조한 다음, 제조된 펠렛을 120 ℃에서 3 시간 동안 열풍건조한 다음 사출기로 시편을 제조하여 각각의 물성을 측정하였으며, 그 결과를 다음 표에 나타내었다.The pellets were extruded and kneaded by an extruder for melt kneading as shown in the following table to prepare pellets. The prepared pellets were hot-air dried at 120 ° C for 3 hours, and specimens were prepared using an injection machine. The results are shown in the following table.

이때, 충격강도는 ASTM D256, 열변형온도는 ASTM D648에 의거 측정하였고, 성형성은 스파이럴플로우(Spiral Flow)에 의한 길이로 평가하였다. 그리고, 내열노화성은 120 ℃ 열풍건조기에서 300 시간을 노화시킨 후, 상온에서 1 시간 방치한 다음 충격강도, 인장강도 및 신율을 측정하여 상온에서 측정한 값보다 변화율이 충격강도는 20% 미만이면 양호, 20% 이상이면 불량인 것으로 하였다. 인장강도는 변화율이 20% 미만이면 양호, 20% 이상이면 불량으로 하고, 인장신율은 80% 미만이면 양호로 80% 이상이면 불량인 것으로 판정하였다.At this time, the impact strength was measured according to ASTM D256, the heat distortion temperature was measured according to ASTM D648, and the formability was evaluated as a spiral flow length. The heat aging resistance was evaluated by measuring the impact strength, tensile strength and elongation after aging in a 120 ° C hot air dryer for 300 hours and then standing at room temperature for 1 hour. When the impact strength was less than 20% , And if it is 20% or more, it is determined to be defective. The tensile strength was determined to be good when the change rate was less than 20%, to be defective when it was 20% or more, and to be inferior if the tensile elongation was 80% or more.

내광노화성은 내후성측정시험기(Fade-O-Meter)의 엔크로스 카본 아크(Enclose carbon arc)하(Black panel 88 ℃)에서 300 시간 조사(照射)한 후, 상온에서 1 시간 방치한 다음 충격강도를 측정하여 상온에서 측정한 충격강도값보다 변화율이 30% 미만이면 양호, 30% 이상이면 불량으로 평가하였다.The photo-aging resistance was measured by irradiating for 300 hours under an Enclose carbon arc (Fade-O-Meter) of Enclose carbon arc (Black panel 88 ° C), leaving it at room temperature for 1 hour, And when the rate of change was less than 30%, it was evaluated as good and when it was 30% or more, it was evaluated as bad.

(주) (1) 점도분자량 25,000인 폴리카보네이트 수지(1) Polycarbonate resin having viscosity and molecular weight of 25,000

(2) 2-(2-히드록시-5-t-옥틸페닐)-벤조트리아졸, UV5411, Cyanamide 사 제품(2) 2- (2-hydroxy-5-t-octylphenyl) -benzotriazole, UV5411, manufactured by Cyanamide

(3) 티오에스테르계 산화방지제, 4,4'-디티오-비스(6-t-부틸-3-메틸페놀), Yoshinox SR, Yoshitomi사 제품(3) thioester antioxidants, 4,4'-dithio-bis (6-t-butyl-3-methylphenol), Yoshinox SR, Yoshitomi

(4) 포스파이트계 산화방지제, 트리스(2,4-디-t-부틸페닐_-포스파이트, MARK 2112, Asahi Denka사 제품(4) phosphite antioxidant, tris (2,4-di-t-butylphenyl-phosphite, MARK 2112, manufactured by Asahi Denka)

(5) 페놀계 산화방지제, 옥타데실-3-(3,5-디-t-부틸-4-히드록시페닐)프로피오네이트, Irganox 1076, Ciba Geigy사 제품(5) Phenolic antioxidants, octadecyl-3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate, Irganox 1076, products of Ciba Geigy

(6) 1/4'', 23 ℃(6) 1/4 '', 23 ° C

(7) 1/4'', -40 ℃(7) 1/4 ", -40 ° C

(8) 1/4'', 18.6 kgf/㎠(8) 1/4 ", 18.6 kgf / cm 2

(9) 120 ℃ × 300 시간(9) 120 占 폚 x 300 hours

(10) 120 ℃ × 300 시간(10) 120 占 폚 x 300 hours

(11) 120 ℃ × 300 시간(11) 120 占 폚 300 hours

(12) 88 ℃ × 300 시간(12) 88 占 폚 占 300 hours

* 아크릴로니트릴-부타디엔-스티렌 수지(ABS 수지) 중에 함유된 부타디엔 고무함량* Butadiene rubber content in acrylonitrile-butadiene-styrene resin (ABS resin)

본 발명에 따른 열가소성 수지 조성물은 내충격성, 내열성, 내열노화성 및 내광노화성이 우수하여 자동차의 인스트루먼트 패널등 상기 물성이 요구되는 부품에 유용하게 사용할 수 있다.The thermoplastic resin composition according to the present invention is excellent in impact resistance, heat resistance, heat aging resistance and photo-aging resistance, and can be usefully used for parts requiring physical properties such as instrument panels for automobiles.

Claims (7)

폴리카보네이트 수지와 아크릴로니트릴-부타디엔-스티렌 수지를 주성분으로 하는 열가소성 수지 조성물에 있어서, 상기 수지 조성물 100 중량부에 벤조트리아졸계 자외선안정제 0.3∼0.5 중량부, 티오에스테르계 산화방지제와 포스파이트계 산화방지제 0.8∼1.2 중량부 및 페놀계 산화방지제 0.4∼0.6 중량부를 첨가하여 이루어진 것을 특징으로 하는 열가소성 수지 조성물.A thermoplastic resin composition comprising, as main components, a polycarbonate resin and an acrylonitrile-butadiene-styrene resin, wherein 0.3 to 0.5 parts by weight of a benzotriazole-based ultraviolet stabilizer, 100 parts by weight of a thioester- 0.8 to 1.2 parts by weight of an antioxidant and 0.4 to 0.6 parts by weight of a phenol-based antioxidant are added to the thermoplastic resin composition. 제1항에 있어서, 상기 아크릴로니트릴-부타디엔-스티렌 수지는 부타디엔 고무를 6∼16 중량% 함유하는 것을 특징으로 하는 열가소성 수지 조성물.The thermoplastic resin composition according to claim 1, wherein the acrylonitrile-butadiene-styrene resin comprises 6 to 16% by weight of a butadiene rubber. 제1항에 있어서, 상기 벤조트리아졸계 자외선안정제는 2-(2-히드록시-5-t-옥틸페닐)-벤조트리아졸 및 2-(5-메틸-2-히드록시-페닐)-벤조트리아졸 중에서 선택된 1 종 이상의 것임을 특징으로 하는 열가소성 수지 조성물.2. The composition of claim 1, wherein the benzotriazole based UV stabilizer is selected from the group consisting of 2- (2-hydroxy-5- t -octylphenyl) -benzotriazole and 2- (5-methyl- Wherein the thermoplastic resin composition is a thermoplastic resin composition. 제1항에 있어서, 상기 티오에스테르계 산화방지제(X)와 포스파이트계 산화방지제(Y) 및 페놀계 산화방지제(Z)의 함량은 다음 수식을 만족시키는 것임을 특징으로 하는 열가소성 수지 조성물.The thermoplastic resin composition according to claim 1, wherein the content of the thioester antioxidant (X), the phosphite antioxidant (Y) and the phenol antioxidant (Z) satisfy the following formula: X + Y ≥ 2Z 이고, X ≥ 2YX + Y? 2Z, and X? 2Y 제1항 또는 제4항에 있어서, 상기 티오에스테르계 산화방지제는 4,4'-디티오-비스(6-t-부틸-3-메틸페놀), 디스테아릴티오 디프로피오네이트 및 디미리스틸티오 디프로피오네이트 중에서 선택된 1 종 이상의 것임을 특징으로 하는 열가소성 수지 조성물.The antioxidant composition according to claim 1 or 4, wherein the thioester antioxidant is at least one selected from the group consisting of 4,4'-dithio-bis (6-t-butyl-3-methylphenol), distearyl thiodipropionate, Wherein the thermoplastic resin composition is at least one selected from the group consisting of styrenesulfonic acid, styrenesulfonic acid, and stilthiodipropionic acid. 제1항 또는 제4항에 있어서, 상기 포스파이트계 산화방지제는 트리스(2,4-디-t-부틸페닐)-포스파이트 및 비스(2,4-디-t-부틸)펜타에리스리톨-디포스파이트 중에서 선택된 1 종 이상의 것임을 특징으로 하는 열가소성 수지 조성물.The positive-type antioxidant according to claim 1 or 4, wherein the phosphite antioxidant is at least one selected from the group consisting of tris (2,4-di- t -butylphenyl) -phosphite and bis (2,4-di- t- butyl) pentaerythritol- Wherein the thermoplastic resin composition is a thermoplastic resin composition. 제1항에 있어서, 상기 페놀계 산화방지제는 옥타데실-3-(3,5-디-t-부틸-4-히드록시페닐)-프로피오네이트, 옥타데실 2,5-디-t-부틸-4-히드록시히드로신나메이트 및 2,5-디-t-부틸-4-sec-부틸페놀 중에서 선택된 1 종 이상의 것임을 특징으로 하는 열가소성 수지 조성물.The method of claim 1 wherein said phenol antioxidant is octadecyl-3- (3,5-di -t- butyl-4-hydroxyphenyl) -propionate, octadecyl-2,5-di-t-butyl -4-hydroxyhydrocinnamate and 2,5-di- t -butyl-4-sec-butylphenol.
KR1019960045725A 1996-10-14 1996-10-14 Thermoplastic resin composition KR100214247B1 (en)

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Cited By (1)

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Publication number Priority date Publication date Assignee Title
KR101184791B1 (en) * 2008-12-31 2012-09-20 주식회사 삼양사 Polycarbonate Resin Composition Having Reduced Mitigation of Pigments onto Mould

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Publication number Priority date Publication date Assignee Title
KR100435519B1 (en) * 1998-10-24 2004-10-06 주식회사 삼양사 Thermoplastic resin composition
KR101636128B1 (en) 2013-07-01 2016-07-04 주식회사 엘지화학 Polycarbonate resin composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101184791B1 (en) * 2008-12-31 2012-09-20 주식회사 삼양사 Polycarbonate Resin Composition Having Reduced Mitigation of Pigments onto Mould

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