KR100654534B1 - Flame retardant thermoplastic resin composition - Google Patents

Flame retardant thermoplastic resin composition Download PDF

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KR100654534B1
KR100654534B1 KR1020050136094A KR20050136094A KR100654534B1 KR 100654534 B1 KR100654534 B1 KR 100654534B1 KR 1020050136094 A KR1020050136094 A KR 1020050136094A KR 20050136094 A KR20050136094 A KR 20050136094A KR 100654534 B1 KR100654534 B1 KR 100654534B1
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compound
weight
resin composition
flame retardant
aromatic vinyl
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김동진
안성희
손세범
최진환
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제일모직주식회사
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/04Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to rubbers
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K3/2279Oxides; Hydroxides of metals of antimony
    • 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
    • C08K5/02Halogenated hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C08L25/02Homopolymers or copolymers of hydrocarbons
    • C08L25/04Homopolymers or copolymers of styrene
    • C08L25/08Copolymers of styrene
    • C08L25/12Copolymers of styrene with unsaturated nitriles
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/04Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/04Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08L27/06Homopolymers or copolymers of vinyl chloride
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/02Flame or fire retardant/resistant
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • 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
    • C08L2666/66Substances characterised by their function in the composition
    • C08L2666/84Flame-proofing or flame-retarding additives

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  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Provided is a flame retardant thermoplastic resin composition which is excellent in weather resistance and flame retardancy without the deterioration of mechanical properties. The thermoplastic resin composition comprises 100 parts by weight of a base resin; 5-30 parts by weight of a halogen-based compound; 1-15 parts by weight of antimony oxide; and 1-10 parts by weight of a chlorine-based organic compound, wherein the base resin comprises (A) an acrylic graft polymer comprising 30-60 wt% of an acrylic synthetic rubber and 40-70 wt% of a copolymer of a cyano vinyl compound and an aromatic vinyl compound; a diene-based graft polymer comprising 30-60 wt% of a diene-based synthetic rubber and 40-70 wt% of a copolymer of a cyano vinyl compound and an aromatic vinyl compound; and a copolymer comprising 20-40 wt% of a cyano vinyl compound and 60-80 wt% of an aromatic vinyl compound.

Description

난연성 열가소성 수지 조성물{Flame Retardant Thermoplastic Resin Composition}Flame Retardant Thermoplastic Resin Composition

본 발명은 난연성 열가소성 수지 조성물에 관한 것으로, 더욱 상세하게는 아크릴계 그라프트 중합체, 디엔계 그라프트 중합체, 시안화비닐 화합물-방향족비닐 화합물 공중합체를 기초 수지로 하여 할로겐계 화합물을 난연제로, 산화안티몬계 화합물을 난연보조제로, 염소계 유기화합물을 충격보강재로 함유하는 우수한 내후성을 갖는 난연성 열가소성 수지 조성물에 관한 것이다.The present invention relates to a flame retardant thermoplastic resin composition, and more particularly, to an acrylic graft polymer, a diene graft polymer, a vinyl cyanide compound-aromatic vinyl compound copolymer, and a halogen-based compound as a flame retardant and an antimony oxide type. A flame retardant thermoplastic resin composition having excellent weather resistance containing a compound as a flame retardant aid and a chlorine-based organic compound as an impact reinforcing material.

일반적으로 아크릴로니트릴-부타디엔-스티렌 수지(이하, 'ABS 수지'라 함)는 내충격성, 기계적 강도, 표면특성 및 가공성 등이 우수하여 전기/전자제품, 자동차 부품 및 일반잡화 등에 광범위하게 사용되고 있는 수지이다. 그러나, 상기 ABS 수지는 수지의 특성상 수지 내부의 고무성분에 화학적으로 불안정한 이중결합을 함유하고 있어서 자외선에 의해 고무성분이 쉽게 노화될 수 있기 때문에 내후성, 내광성이 좋지 못하여, 옥외에 오랜 시간 방치할 경우, 시간이 지남에 따라 변색 및 물성저하가 비교적 커서 일광에 노출되어 있는 옥외 용도에 적합하지 못한 문제점이 있다. Generally, acrylonitrile-butadiene-styrene resin (hereinafter referred to as 'ABS resin') is widely used in electric / electronic products, automobile parts, and general merchandise because of its excellent impact resistance, mechanical strength, surface properties, and workability. Resin. However, the ABS resin contains a chemically unstable double bond in the rubber component of the resin due to the characteristics of the resin, so that the rubber component can be easily aged by ultraviolet rays, so the weather resistance and light resistance are not good, and when it is left outdoors for a long time However, over time, discoloration and physical property deterioration are relatively large, which makes it unsuitable for outdoor use exposed to sunlight.

따라서, 이러한 문제점을 보완하기 위해 ABS 수지 성형품에 도장 또는 도금과 같은 후가공을 하거나, ABS 수지의 압출가공시 자외선 안정제를 다량 첨가하는 방법을 사용하고 있으나 전자는 공정이 복잡하고 불량율이 높은 단점이 있고, 후자는 제조원가 상승과 만족할 만한 장시간의 내후성을 얻지 못하는 단점이 있다.Therefore, in order to compensate for this problem, a post-processing such as painting or plating is applied to the ABS resin molded article or a method of adding a large amount of UV stabilizer during extrusion processing of the ABS resin, but the former has a disadvantage in that the process is complicated and the defect rate is high. However, the latter has the disadvantage of failing to obtain a rise in manufacturing cost and satisfactory long-term weather resistance.

이와 같은 ABS 수지의 용도의 한계를 극복하기 위하여 ABS 수지 대신에 내후성이 우수하다고 알려져 있는 여러 수지들을 사용하고 있는데, 이중 아크릴레이트-스티렌-아크릴로니트릴 수지(이하, 'ASA 수지'라 함)가 가장 널리 사용되고 있다.In order to overcome the limitations of the use of ABS resins, various resins are known to have excellent weather resistance instead of ABS resins. Of these, acrylate-styrene-acrylonitrile resins (hereinafter referred to as 'ASA resins') are used. Most widely used.

ASA 수지는 일반적으로 아크릴계 합성고무에 시안화비닐 화합물과 방향족비닐 화합물을 유화 그라프트 중합방법에 의해 그라프트 중합한 아크릴계 그라프트 중합체와 시안화비닐 화합물 및 방향족비닐 화합물을 공중합시킨 시안화비닐 화합물-방향족비닐 화합물 공중합체를 혼합, 압출 가공하여 제조된다. 이때, 사용되는 아크릴계 합성고무와 아크릴계 그라프트 중합체, 그리고 매트릭스 중합체인 시안화비닐 화합물-방향족비닐 화합물 공중합체의 물성과 함량을 조절하고 특정한 역할의 보강재를 선택적으로 더 첨가하면 원하는 물성의 수지를 얻을 수 있다. ASA resins are generally vinyl cyanide compounds-aromatic vinyl compounds obtained by copolymerizing an acrylic graft polymer, a vinyl cyanide compound, and an aromatic vinyl compound graft-polymerized with an acrylic synthetic rubber by an emulsion graft polymerization method. The copolymer is prepared by mixing and extruding. At this time, by controlling the physical properties and content of the acrylic synthetic rubber and acrylic graft polymer, and the matrix polymer, the vinyl cyanide compound-aromatic vinyl compound copolymer, and selectively adding a reinforcing material of a specific role, the desired physical resin can be obtained. have.

이렇게 제조된 ASA 수지는 내후성, 내광성, 내약품성, 내열성 등이 우수하기 때문에 옥외용 전기/전자제품, 자동차용 외장부품, 건축용 자재 등 일광노출이 많은 옥외용 외장부품에 사용하기에 적합하다. 반면, ASA 수지는 그 자체로는 연소에 대한 저항성이 없고, 외부의 점화인자에 의해 불꽃이 점화되면 수지 자체가 연소를 도와주는 에너지로 작용하여 지속적으로 불을 확산시키게 되는 문제점이 있 다. Thus prepared ASA resin is excellent in weather resistance, light resistance, chemical resistance, heat resistance, etc., so it is suitable for use in outdoor exterior parts with high exposure to sunlight, such as outdoor electrical / electronic products, automotive exterior parts, building materials. On the other hand, ASA resin itself is not resistant to combustion, and when a spark is ignited by an external ignition factor, there is a problem in that the resin itself acts as an energy to assist combustion and continuously spreads fire.

따라서, 미국, 유럽 등의 국가에서는 전기·전자제품 등의 화재에 대한 안정성 확보를 위하여 난연성을 갖는 수지를 전기·전자제품 내외장 부품의 성형품 제조에 사용하도록 법제화하고 있다.Therefore, in the United States, Europe, etc., in order to secure stability against fires of electric and electronic products, a resin having flame retardancy is used to manufacture molded articles of internal and external parts of electric and electronic products.

ASA 수지의 제조방법으로는 아크릴계 고무를 사용하여 아크릴로니트릴과 스티렌을 공중합하는 방법(미국특허 제4,753,988호, 제4,801,646호 및 일본특허 특개소 60-3350호, 특공소 59-15331호), 폴리부타디엔 고무와 아크릴계 고무를 혼합한 고무에 아크릴로니트릴과 스티렌을 공중합하는 방법(일본특허 특개소 57-212215호, 특개소 58-187411호 및 특개소 57-167308호) 등이 개시되어 있으나, 이들 종래기술에는 ASA 수지의 난연성을 부여하는 방법은 개시되어 있지 않은 실정이다.As a method for producing ASA resin, a method of copolymerizing acrylonitrile and styrene using an acrylic rubber (US Pat. Nos. 4,753,988, 4,801,646, and Japanese Patent Application Laid-Open No. 60-3350, Special Publication 59-15331), poly A method of copolymerizing acrylonitrile and styrene on rubber mixed with butadiene rubber and acrylic rubber (Japanese Patent Laid-Open Nos. 57-212215, 58-187411 and 57-167308) is disclosed. In the prior art, a method of imparting flame retardancy of ASA resin is not disclosed.

이에 본 발명자들은 상기와 같은 종래기술의 문제점을 해결하기 위하여 ABS 수지의 내후성을 향상시키고자 ABS 수지 대신 ASA 수지를 사용하고, 또한 난연성을 향상시키고자 할로겐을 함유한 유기화합물을 난연제로, 산화안티몬을 함유한 무기화합물을 난연보조제로 첨가함으로써 본 발명을 완성하게 되었다. In order to solve the problems of the prior art, the present inventors use ASA resin instead of ABS resin to improve the weather resistance of the ABS resin, and to improve the flame retardancy, an organic compound containing halogen as a flame retardant, antimony oxide The present invention was completed by adding an inorganic compound containing a flame retardant aid.

따라서, 본 발명은 상기와 같은 문제점을 해결하기 위한 것으로, ASA 수지에 할로겐계 난연제 및 산화안티몬을 첨가함으로써 내후성이 우수한 난연성 열가소성 수지 조성물을 제공함을 목적으로 한다.Accordingly, an object of the present invention is to provide a flame retardant thermoplastic resin composition having excellent weather resistance by adding a halogen flame retardant and antimony oxide to an ASA resin.

본 발명은 하기 (A)+(B) : (C)의 중량비가 20∼60 : 40∼80이고, (A) : (B)의 중량비가 50∼90 : 10∼50인 기초 수지 (A)+(B)+(C) 100 중량부에 대하여 할로겐계 화합물 5∼30 중량부, 산화안티몬 1∼15 중량부 및 염소 유기화합물 1∼10 중량부를 포함하는 난연성 열가소성 수지 조성물임을 특징으로 한다.The present invention is a base resin (A) having a weight ratio of (A) + (B) :( C) of 20 to 60:40 to 80, and a weight ratio of (A) to (B) of 50 to 90:10 to 50. A flame retardant thermoplastic resin composition comprising 5 to 30 parts by weight of a halogen compound, 1 to 15 parts by weight of antimony oxide, and 1 to 10 parts by weight of chlorine organic compound, based on 100 parts by weight of + (B) + (C).

(A) 아크릴계 합성고무 30∼60 중량%와 시안화비닐 화합물-방향족비닐 화합물 공중합체 40∼70 중량%로 이루어진 아크릴계 그라프트 중합체 ;(A) Acrylic graft polymer which consists of 30-60 weight% of acrylic synthetic rubbers and 40-70 weight% of a vinyl cyanide compound-aromatic vinyl compound copolymer;

(B) 디엔계 합성고무 30∼60 중량%와 시안화비닐 화합물-방향족비닐 화합물 공중합체 40∼70 중량%로 이루어진 디엔계 그라프트 중합체 ;(B) a diene graft polymer composed of 30 to 60 wt% of a diene synthetic rubber and 40 to 70 wt% of a vinyl cyanide compound-aromatic vinyl compound copolymer;

(C) 시안화비닐 화합물 20∼40 중량%와 방향족비닐 화합물 60∼80 중량%로 이루어진 시안화비닐 화합물-방향족비닐 화합물 공중합체.(C) Vinyl cyanide compound-aromatic vinyl compound copolymer which consists of 20-40 weight% of vinyl cyanide compounds and 60-80 weight% of aromatic vinyl compounds.

이하, 본 발명을 상세히 설명한다.Hereinafter, the present invention will be described in detail.

(A) 아크릴계 그라프트 중합체(A) Acrylic Graft Polymer

본 발명에 의한 열가소성 수지조성물에 사용되는 아크릴계 그라프트 중합체는 아크릴계 합성고무에 시안화비닐 화합물과 방향족비닐 화합물의 단량체 혼합물을 혼합하여 통상의 유화 그라프트 중합방법에 의하여 제조한다. The acrylic graft polymer used in the thermoplastic resin composition according to the present invention is prepared by a conventional emulsion graft polymerization method by mixing a monomer mixture of a vinyl cyanide compound and an aromatic vinyl compound in an acrylic synthetic rubber.

상기 시안화비닐 화합물과 방향족비닐 화합물의 단량체 혼합물은 고형분 기준으로 20∼30 중량%의 시안화비닐 화합물과 70∼80 중량%의 방향족비닐 화합물이 사용되는데, 아크릴계 합성고무에 그라프트되어 있는 시안화비닐 화합물-방향족비 닐 화합물 공중합체는 전체 아크릴계 그라프트 중합체에 대하여 40∼70 중량%인 것이 바람직하다.As the monomer mixture of the vinyl cyanide compound and the aromatic vinyl compound, 20 to 30% by weight of a vinyl cyanide compound and 70 to 80% by weight of an aromatic vinyl compound are used, and the vinyl cyanide compound grafted on the acrylic synthetic rubber- The aromatic vinyl compound copolymer is preferably 40 to 70% by weight based on the total acrylic graft polymer.

또한, 상기 아크릴계 그라프트 중합체를 제조하기 위한 아크릴계 합성고무는 탄소수 2∼8개의 알킬아크릴레이트로부터 합성된 것이 바람직하고, 아크릴계 합성고무 입자의 평균입경은 0.05∼0.5 ㎛의 범위가 가능하며, 0.1∼0.3 ㎛의 범위가 바람직하다.In addition, the acrylic synthetic rubber for producing the acrylic graft polymer is preferably synthesized from an alkyl acrylate having 2 to 8 carbon atoms, the average particle diameter of the acrylic synthetic rubber particles may be in the range of 0.05 to 0.5 ㎛, 0.1 ~ The range of 0.3 micrometer is preferable.

본 발명에 의한 수지 조성물에 사용되는 아크릴계 그라프트 중합체를 제조하기 위한 시안화비닐 화합물로는 아크릴로니트릴, 메타크릴로니트릴 등이 있으며, 이들은 단독 또는 혼합하여 사용될 수 있고, 또한 상기 아크릴계 그라프트 중합체를 제조하기 위한 방향족비닐 화합물로는 스티렌, 알파-메틸스티렌, p-t-부틸스티렌, 2,4-디메틸스티렌, 비닐톨루엔 등이 있으며, 이들은 단독 또는 혼합하여 사용될 수 있다.Vinyl cyanide compounds for preparing the acrylic graft polymer used in the resin composition according to the present invention include acrylonitrile, methacrylonitrile, and the like, and these may be used alone or in combination. Aromatic vinyl compounds for preparation include styrene, alpha-methylstyrene, pt-butylstyrene, 2,4-dimethylstyrene, vinyltoluene and the like, which may be used alone or in combination.

(B) 디엔계 그라프트 중합체(B) diene graft polymer

본 발명에 의한 수지 조성물에 사용되는 디엔계 그라프트 중합체는 디엔계 합성고무에 시안화비닐 화합물과 방향족비닐 화합물의 단량체 혼합물를 혼합하여 통상의 유화 그라프트 중합방법에 의하여 제조한다. The diene graft polymer used in the resin composition according to the present invention is prepared by a conventional emulsion graft polymerization method by mixing a diene-based synthetic rubber with a monomer mixture of a vinyl cyanide compound and an aromatic vinyl compound.

상기 시안화비닐 화합물과 방향족비닐 화합물의 단량체 혼합물은 고형분 기준으로 20∼30 중량%의 시안화비닐 화합물과 80∼70 중량%의 방향족비닐 화합물로 이루어지며, 디엔계 합성고무에 그라프트되어 있는 시안화비닐 화합물-방향족비닐 화합물 공중합체는 전체 디엔계 그라프트 중합체에 대하여 40∼70 중량%인 것이 바람직하다.The monomer mixture of the vinyl cyanide compound and the aromatic vinyl compound is composed of 20 to 30% by weight of vinyl cyanide compound and 80 to 70% by weight of aromatic vinyl compound on the basis of solid content, and vinyl cyanide compound grafted on the diene-based synthetic rubber. The aromatic vinyl compound copolymer is preferably 40 to 70% by weight based on the total diene graft polymer.

또한, 상기 디엔계 그라프트 중합체를 제조하기 위한 디엔계 합성고무는 폴리부타디엔, 폴리이소프렌, 폴리클로로프렌, 부타디엔-스티렌 공중합체, 부타디엔-아크릴로니트릴 공중합체 등이 있으며, 이 중에서 폴리부타디엔, 부타디엔-스티렌 공중합체, 부타디엔-아크릴로니트릴 공중합체가 바람직하고, 상기 디엔계 합성고무 입자의 평균입경은 0.1∼0.6 ㎛인 범위가 바람직하며, 0.2∼0.5 ㎛인 범위가 좀더 바람직하다.In addition, the diene-based synthetic rubber for preparing the diene-based graft polymer may include polybutadiene, polyisoprene, polychloroprene, butadiene-styrene copolymer, butadiene-acrylonitrile copolymer, and the like, and polybutadiene, butadiene- Styrene copolymers and butadiene-acrylonitrile copolymers are preferred, and the average particle diameter of the diene-based synthetic rubber particles is preferably in the range of 0.1 to 0.6 mu m, more preferably in the range of 0.2 to 0.5 mu m.

본 발명에 의한 난연성 열가소성 수지 조성물에 사용되는 디엔계 그라프트 중합체를 제조하기 위한 시안화비닐 화합물로는 아크릴로니트릴, 메타크릴로니트릴 등이 있으며, 이들은 단독 또는 혼합하여 사용될 수 있고, 또한 디엔계 그라프트 중합체를 제조하기 위한 방향족비닐 화합물로는 스티렌, 알파-메틸스티렌, p-t-부틸스티렌, 2,4-디메틸스티렌, 비닐톨루엔 등이 있으며, 이들은 단독 또는 혼합하여 사용될 수 있다.Vinyl cyanide compounds for producing the diene graft polymer used in the flame retardant thermoplastic resin composition according to the present invention include acrylonitrile, methacrylonitrile, and the like. Aromatic vinyl compounds for the production of the polymers include styrene, alpha-methylstyrene, pt-butylstyrene, 2,4-dimethylstyrene, vinyltoluene, and the like, which may be used alone or in combination.

(C) 시안화비닐 화합물-방향족비닐 화합물 공중합체(C) Vinyl Cyanide Compound-Aromatic Vinyl Compound Copolymer

본 발명에 의한 수지 조성물에 사용되는 시안화비닐 화합물-방향족비닐 화합물 공중합체는 고형분 기준으로 시안화비닐 화합물 20∼40 중량%와 방향족비닐 화합물 60∼80 중량%를 사용하여 통상의 중합방법으로 제조되며, 중량 평균분자량이 80,000∼400,000 범위인 것이 바람직한데, 상기 시안화비닐 화합물-방향족비닐 화 합물 공중합체(C)의 중량 평균분자량이 80,000 보다 낮을 경우 내충격성이 현저히 저하되고, 400,000 보다 높을 경우 유동성이 낮아 성형품을 가공하는데 어려움이 있다.The vinyl cyanide compound-aromatic vinyl compound copolymer used in the resin composition according to the present invention is prepared by a conventional polymerization method using 20 to 40% by weight of a vinyl cyanide compound and 60 to 80% by weight of an aromatic vinyl compound on a solids basis. It is preferable that the weight average molecular weight is in the range of 80,000 to 400,000. When the weight average molecular weight of the vinyl cyanide compound-aromatic vinyl compound copolymer (C) is lower than 80,000, impact resistance is significantly lowered, and when higher than 400,000, fluidity is low. Difficulties in processing the molded article.

본 발명에 의한 수지 조성물에 사용되는 시안화비닐 화합물-방향족비닐 화합물 공중합체를 구성하는 시안화비닐 화합물로는 아크릴로니트릴, 메타크릴로니트릴 등의 단독 혹은 혼합물이 사용될 수 있다. 한편, 상기 방향족비닐 화합물로는 스티렌, 알파-메틸스티렌, p-t-부틸스티렌, 2,4-디메틸스티렌, 비닐톨루엔 등의 단독 또는 그 혼합물이 사용될 수 있고, 또한 이들과 N-페닐말레이미드, N-시클로헥실말레이드, 무수말레인산 등이 공중합될 수 있으며, 제조방법으로는 유화중합법, 현탁중합법, 용액중합법, 괴상중합법 등이 적용 가능하다.As the vinyl cyanide compound constituting the vinyl cyanide compound-aromatic vinyl compound copolymer used in the resin composition of the present invention, an acrylonitrile, methacrylonitrile or the like or a mixture thereof may be used. As the aromatic vinyl compound, styrene, alpha-methyl styrene, pt-butyl styrene, 2,4-dimethyl styrene, vinyl toluene or the like or a mixture thereof may be used, and these and N-phenylmaleimide, N Cyclohexyl maleade, maleic anhydride, and the like may be copolymerized, and as the production method, an emulsion polymerization method, suspension polymerization method, solution polymerization method, or bulk polymerization method may be applied.

(D) 할로겐계 화합물(D) halogen-based compound

본 발명에 의한 수지 조성물에 사용되는 할로겐계 화합물은 난연제로 사용되며, 상업화되어 일반적으로 사용되는 할로겐계 화합물이 사용될 수 있다. 구체적 예로 테트라브로모비스페놀 A (Tetrabromobisphenol A), 비스(트리브로모페녹시)에탄(Bis(Tribromophenoxy) ethane), 브롬화 에폭시 수지(Brominated epoxy resin) 또는 에폭시말단이 트리브로모페놀로 치환된 브롬화 에폭시 수지(Brominated epoxy resin terminated with tribromophenol), 2,4,6-트리(2,4,6-트리브로모페녹시)-1,3,5-트리아진 등이 사용 가능하다.The halogen-based compound used in the resin composition according to the present invention may be used as a flame retardant, and a halogen-based compound commercially used and generally used may be used. Specific examples include tetrabromoobisphenol A, bibro (tribromophenoxy) ethane, brominated epoxy resin, or brominated epoxy in which the epoxy terminal is substituted with tribromophenol. Brominated epoxy resin terminated with tribromophenol, 2,4,6-tri (2,4,6-tribromophenoxy) -1,3,5-triazine can be used.

상기 할로겐계 화합물은 기초 수지 (A)+(B)+(C) 100 중량부에 대하여 5 내 지 30 중량부의 양으로 사용되는데, 5 중량부 미만으로 사용할 경우에는 난연효과가 떨어지고, 30 중량부를 초과하여 사용할 경우에는 가공성 및 기계적 강도가 저하되는 문제점이 발생하여 물성상의 균형을 잃게 되므로 바람직하지 않게 된다. The halogen-based compound is used in an amount of 5 to 30 parts by weight based on 100 parts by weight of the base resin (A) + (B) + (C), but when used less than 5 parts by weight, the flame retardant effect is reduced, and 30 parts by weight When used in excess, the problem occurs that the workability and mechanical strength are deteriorated and the balance of physical properties is lost, which is not preferable.

(E) 산화안티몬(E) antimony oxide

본 발명에 의한 수지 조성물에 사용되는 산화안티몬은 난연제로 사용되는 할로겐계 화합물과 상승작용을 일으켜 ASA 수지에 적정한 난연성을 부여하기 위하여 난연보조제로 사용되며, 그 예로는 삼산화안티몬 또는 오산화안티몬 등이 있다. The antimony oxide used in the resin composition according to the present invention is used as a flame retardant aid to synergize with the halogen-based compound used as a flame retardant to impart proper flame retardancy to the ASA resin, and examples thereof include antimony trioxide or antimony pentoxide. .

상기 산화안티몬의 함량은 기초 수지 (A)+(B)+(C) 100 중량부에 대하여 1 내지 15 중량부를 사용하는 것이 바람직한데, 산화안티몬을 1 중량부 미만으로 사용하는 경우에는 충분한 난연효과를 얻을 수 없으며, 15 중량부를 초과하여 과량 사용하였을 경우에는 수지 조성물의 물성상의 균형을 잃게 되므로 바람직하지 않다.The content of the antimony oxide is preferably used 1 to 15 parts by weight based on 100 parts by weight of the base resin (A) + (B) + (C), when the antimony oxide is used in less than 1 part by weight sufficient flame retardant effect It cannot be obtained, and when it is used in excess of 15 parts by weight, it is not preferable because the balance of physical properties of the resin composition is lost.

(F) 염소유기화합물(F) chlorine organic compounds

본 발명에 의한 수지 조성물에 사용되는 염소 유기화합물은 난연보조제 및 충격보강제로 사용될 수 있는데, 본 발명에서 염소 유기화합물이란 염소가 치환 또는 첨가 등이 되어 염소를 포함하고 있는 유기화합물을 일컫는 것으로, 그 예로는 염소화폴리에틸렌(chlorinated polyethylene, CPE), 폴리비닐클로라이드(PVC)를 사용할 수 있으며, 이 중 염소화폴리에틸렌(chlorinated polyethylene, CPE)이 특히 바람직하다.The chlorine organic compound used in the resin composition according to the present invention may be used as a flame retardant adjuvant and an impact modifier. In the present invention, the chlorine organic compound refers to an organic compound containing chlorine due to substitution or addition of chlorine. Examples include chlorinated polyethylene (CPE) and polyvinyl chloride (PVC), of which chlorinated polyethylene (CPE) is particularly preferred.

상기 염소 유기화합물의 함량은 기초 수지 (A)+(B)+(C) 100 중량부에 대하여 1 내지 10 중량부인데, 1 중량부 미만으로 사용할 경우 충분한 난연보조효과 및 충격강도를 얻을 수 없으며, 10 중량부를 초과할 경우 열안정성이 현저히 떨어지는 단점이 있다.The content of the chlorine organic compound is 1 to 10 parts by weight based on 100 parts by weight of the base resin (A) + (B) + (C), but when used less than 1 part by weight, sufficient flame retardant auxiliary effect and impact strength cannot be obtained. If it exceeds 10 parts by weight, thermal stability is significantly lower.

본 발명에 의한 난연성 열가소성 수지 조성물은 기초 수지 (A)+(B)+(C) 100 중량부에 대하여 (A)+(B) : (C)의 중량비는 60 : 40 내지 20 : 80의 범위가 바람직한데, (A)+(B)의 중량이 기초 수지에 대하여 60 중량부를 초과할 경우 유동성이 현저히 저하되고, 20 중량부 보다 적은 경우 충격강도가 저하되어 실용적이지 못하다. The flame retardant thermoplastic resin composition according to the present invention has a weight ratio of (A) + (B) :( C) to 100 parts by weight of the base resin (A) + (B) + (C) in the range of 60:40 to 20:80 When the weight of (A) + (B) exceeds 60 parts by weight with respect to the base resin, the fluidity is significantly lowered, and when it is less than 20 parts by weight, the impact strength is lowered, which is not practical.

또한, (A) : (B)의 중량비는 90 : 10 내지 50 : 50의 범위가 바람직한데, (A)의 중량비가 90 보다 큰 경우, 충격강도가 저하되어 실용적이지 못하고, (A)의 중량비가 50 보다 작은 경우, 내후성이 충분하지 않아 내후 수지로서의 가치가 떨어진다. In addition, the weight ratio of (A) :( B) is preferably in the range of 90:10 to 50:50, but when the weight ratio of (A) is greater than 90, the impact strength is lowered and is not practical, and the weight ratio of (A) When is less than 50, weather resistance is not enough and the value as a weathering resin falls.

본 발명에 의한 난연성 열가소성 수지 조성물은 각각의 용도에 따라 선택적으로 특정한 산화방지제, 활제, 충격보강제, 광안정제, 충진제, 무기물 첨가제, 안료 및/또는 염료 등을 더 첨가하여 제조할 수 있다. 즉, 본 발명에 의한 수지 조성물은 상기 (A) 내지 (F)를 포함하여 이루어지는 수지 조성물에 그 용도 및 필요에 따라 틴말레이트계 화합물 또는 알루미노실리케이트계 무기 화합물, 왁스, 금속활제, 산화방지제, 광안정제, 안료 및 염료로 이루어진 군으로부터 선택된 1종 이상의 물질을 더 포함할 수 있다. The flame-retardant thermoplastic resin composition according to the present invention may be prepared by further adding a specific antioxidant, lubricant, impact modifier, light stabilizer, filler, inorganic additive, pigment and / or dye, etc. according to each use. That is, the resin composition according to the present invention is a tin maleate compound or an aluminosilicate inorganic compound, a wax, a metal lubricant, an antioxidant, according to the use and need thereof in the resin composition comprising the above (A) to (F). It may further comprise one or more materials selected from the group consisting of light stabilizers, pigments and dyes.

상기 틴말레이트계 화합물 또는 알루미노실리케이트계 무기 화합물은 할로겐계 난연제를 사용할 때 할로겐 캡쳐 역할을 하여 수지조성물의 변색을 방지하는 난연 열안정제 역할을 하는데, 상기 기타 첨가물의 사용량은 상기 기초 수지 (A)+(B)+(C) 100 중량부에 대하여 30 중량부 이하로 추가로 포함할 수 있다.The tin maleate compound or aluminosilicate inorganic compound acts as a flame retardant heat stabilizer to prevent discoloration of the resin composition by acting as a halogen capture when using a halogen-based flame retardant, the amount of the other additives is used as the base resin (A) It may further include up to 30 parts by weight based on 100 parts by weight of + (B) + (C).

본 발명에 의한 난연성 열가소성 수지 조성물의 제조방법은 본 발명이 속하는 기술분야에서 이미 공지되어 있으며, 본 발명의 열가소성 수지 조성물 또한 상기 통상의 방법에 의해 제조될 수 있다. 그러나 하나의 구현예를 들면,The method for producing a flame retardant thermoplastic resin composition according to the present invention is already known in the art to which the present invention pertains, and the thermoplastic resin composition of the present invention may also be prepared by the conventional method. However, for one embodiment,

(가) 상기 ASA 수지(A)+(B)+(C)를 난연제인 할로겐 화합물(D)와 혼합하고, 상기 혼합물에 난연보조제인 산화안티몬(E), 충격보강제인 염소유기화합물(F) 및 선택적으로 무기 첨가제, 왁스, 금속활제, 산화방지제, 광안정제, 안료 및 염료로 이루어진 군으로부터 선택된 1종 이상의 물질을 첨가하는 단계;(A) The ASA resin (A) + (B) + (C) is mixed with a halogen compound (D), which is a flame retardant, and the mixture is a flame retardant, antimony oxide (E), an impact modifier, a chlorine organic compound (F). And optionally adding at least one material selected from the group consisting of inorganic additives, waxes, metal lubricants, antioxidants, light stabilizers, pigments and dyes;

(나) 상기 첨가된 성분들을 혼합기에서 혼합하는 단계; 및(B) mixing the added ingredients in a mixer; And

(다) 상기 혼합물을 압출하는 단계를 포함하는 방법에 의해 제조될 수 있으며, 보다 구체적으로는 상기의 (A) 내지 (F)의 각 구성성분에 할로겐 캡쳐로서 틴말레이트계 화합물 또는 알루미노실리케이트계 무기 화합물, 산화방지제, 금속활제, 왁스, 이산화티타늄, 벤조트리아졸 및 힌더드 아민계 광안정제를 첨가한 후, 이를 통상의 혼합기에서 혼합하고, 상기 혼합물을 압출기를 통해 압출하여 펠렛 형태의 수지 조성물로 제조할 수 있다.(C) can be prepared by a method comprising the step of extruding the mixture, more specifically a tin maleate-based compound or aluminosilicate-based compound as a halogen capture to each component of the above (A) to (F) After adding an inorganic compound, an antioxidant, a metal lubricant, a wax, titanium dioxide, benzotriazole and a hindered amine light stabilizer, they are mixed in a conventional mixer, and the mixture is extruded through an extruder to form a resin composition in pellet form. It can be prepared as.

본 발명에 의한 수지 조성물은 하기의 실시예에 의하여 보다 더 잘 이해될 수 있으나, 하기의 실시예는 본 발명을 예시하기 위한 목적으로서 본 발명의 보호 범위를 제한하고자 하는 것은 아니다. The resin composition according to the present invention may be better understood by the following examples, but the following examples are not intended to limit the protection scope of the present invention for the purpose of illustrating the present invention.

실시예Example

하기의 실시예 및 비교예에서 사용된 (A) 아크릴계 그라프트 중합체, (B) 디엔계 그라프트 중합체, (C) 시안화비닐 화합물-방향족비닐 화합물 공중합체, (D) 할로겐계 화합물, (E) 산화안티몬 및 (F) 염소유기화합물의 사양은 다음과 같다. 할로겐계 화합물, 산화안티몬, 염소유기화합물 및 기타 첨가물은 상업적으로 입수할 수 있는 제품을 추가 정제 등의 과정 없이 그대로 사용하였다.(A) acrylic graft polymer, (B) diene graft polymer, (C) vinyl cyanide compound-aromatic vinyl compound copolymer, (D) halogen compound, (E) used in the following Examples and Comparative Examples The specifications of antimony oxide and (F) chlorine organic compounds are as follows. Halogen-based compounds, antimony oxide, chlorine organic compounds and other additives were used as such without commercially available products.

(A) 아크릴계 그라프트 중합체(A) Acrylic Graft Polymer

부틸아크릴레이트 고무 50 중량부에 아크릴로니트릴 25 중량%과 스티렌 75 중량%로 이루어진 단량체 혼합물 100 중량부를 그라프트 유화중합한 고무입경이 약 0.2 ㎛인 코어-쉘 형태의 그라프트 ASA 수지를 사용하였다. 100 parts by weight of a monomer mixture composed of 25% by weight of acrylonitrile and 75% by weight of styrene acrylate rubber was used as a core-shell graft ASA resin having a rubber particle diameter of about 0.2 μm. .

(B) 디엔계 그라프트 중합체(B) diene graft polymer

부타디엔 고무 58 중량부에 아크릴로니트릴 25 중량%과 스티렌 75 중량%로 이루어진 단량체 혼합물 100 중량부를 그라프트 유화중합한 고무입경이 약 0.3 ㎛인 코어-쉘 형태의 그라프트 ABS 수지를 사용하였다. A core-shell graft ABS resin having a rubber particle size of about 0.3 μm of a graft emulsion-polymerized rubber was used in 58 parts by weight of butadiene rubber in an amount of 100 parts by weight of a monomer mixture composed of 25% by weight of acrylonitrile and 75% by weight of styrene.

(C) 시안화비닐 화합물-방향족비닐 화합물 공중합체(C) Vinyl Cyanide Compound-Aromatic Vinyl Compound Copolymer

아크릴로니트릴 함량이 28 중량%, 스티렌 함량이 72 중량%이고 중량평균분자량이 약 120,000인 스티렌-아크릴로니트릴 공중합체 수지(이하, 'SAN 수지'라 함)를 사용하였다.A styrene-acrylonitrile copolymer resin (hereinafter referred to as 'SAN resin') having an acrylonitrile content of 28% by weight, a styrene content of 72% by weight, and a weight average molecular weight of about 120,000 was used.

(D) 할로겐계 화합물(D) halogen-based compound

중량평균 분자량이 550인 미국 ALBERMALE社 제조 TBBA계통의 난연제인 SAYTEX RB 100을 사용하였다.SAYTEX RB 100, a flame retardant of the TBBA system manufactured by ALBERMALE, USA having a weight average molecular weight of 550 was used.

(E) 산화 안티몬(E) antimony oxide

본 발명에 의한 열가소성 수지 조성물에 함유되는 산화 안티몬으로는 삼산화안티몬(한국 일성안티몬社 제조)을 사용하였다. As antimony oxide contained in the thermoplastic resin composition according to the present invention, antimony trioxide (manufactured by Ilsung Antimony Co., Ltd.) was used.

(F) 염소 유기화합물(F) chlorine organic compounds

본 발명에 의한 열가소성 수지 조성물에 함유되는 염소 유기화합물로는 미국 DDE사의 클로리네이티드 폴리에틸렌(CPE) Tyrin 3245P를 사용하였다. As the chlorine organic compound contained in the thermoplastic resin composition according to the present invention, US DDE's Chlorinated Polyethylene (CPE) Tyrin 3245P was used.

실시예Example 1 내지  1 to 실시예Example 4 4

상기 각 구성성분을 하기 표 1에 기재된 바와 같은 함량으로 첨가하고, 할로겐 캡쳐로서 틴말레이트계 화합물 TM-600P(송원산업社, 한국) 1.0 중량부, 산화방지제로서 hindered phenol계 산화방지제인 Irganox1076(송원산업社, 한국) 0.3 중 량부, 스테아린산계 금속활제인 SONGSTAB Ca-ST(송원산업社, 한국) 0.4 중량부 및 왁스 1 중량부를 첨가하여 믹서로 균일하게 혼합한 후, 이축압출기로 압출하여 펠렛 형태의 난연성 열가소성 수지 조성물을 제조하였다.Each component is added in an amount as shown in Table 1 below, 1.0 parts by weight of tin maleate compound TM-600P (Songwon Industrial Co., Korea) as a halogen capture, Irganox1076 (Songwon, a hindered phenolic antioxidant as an antioxidant) Industries, Korea) 0.3 parts by weight, 0.4 parts by weight of SONGSTAB Ca-ST (Songwon Industry Co., Korea), a stearic acid-based metal lubricant, and 1 part by weight of wax are mixed uniformly with a mixer, and then extruded with a twin screw extruder to form pellets. A flame retardant thermoplastic resin composition was prepared.

비교예Comparative example 1 One

(A)그라프트 ASA 수지를 사용하지 않고 (B)그라프트 ABS 수지 만 단독 사용한 것을 제외하고는 상기 실시예 1과 동일하게 실시하여 펠렛 형태의 난연성 열가소성 수지 조성물을 제조하였다.A flame-retardant thermoplastic resin composition was prepared in the same manner as in Example 1 except that (A) graft ASA resin was not used and only (B) graft ABS resin was used.

비교예Comparative example 2 2

(B)그라프트 ABS 수지를 사용하지 않고 (A)그라프트 ASA 수지 만 단독 사용한 것을 제외하고는 상기 실시예 1과 동일하게 실시하여 펠렛 형태의 난연성 열가소성 수지 조성물을 제조하였다.A flame-retardant thermoplastic resin composition was prepared in the same manner as in Example 1 except that (B) graft ABS resin was not used and only (A) graft ASA resin was used.

비교예Comparative example 3 3

난연제인 할로겐계 화합물과 난연보조제인 산화안티몬을 사용하지 않은 것을 제외하고는 상기 실시예 2와 동일하게 실시하여 펠렛 형태의 난연성 열가소성 수지 조성물을 제조하였다.A flame retardant thermoplastic resin composition was prepared in the same manner as in Example 2 except that a halogen-based compound as a flame retardant and an antimony oxide as a flame retardant were not used.

[표 1]TABLE 1

Figure 112005078647607-pat00001
Figure 112005078647607-pat00001

시험예Test Example

상기 실시예 1 내지 실시예 4 및 비교예 1 내지 비교예 3에서 제조된 펠렛 형태의 수지 조성물로부터 사출성형에 의해 물성 및 난연 시험용 시편 등을 제작하여 충격강도, 유동성, 내후성 및 난연성 등을 측정하였는 바, 각 물성항목에 대한 측정결과를 하기 표 2에 나타내었다.From the resin composition of the pellet form prepared in Examples 1 to 4 and Comparative Examples 1 to 3 by the injection molding to test the physical properties and flame retardant test, etc. to measure the impact strength, fluidity, weather resistance and flame retardancy Bar, the measurement results for each property item are shown in Table 2 below.

충격강도 측정은 ASTM D-256 시험 방법에 의해 1/4 인치 두께에 대해 평가하였으며 단위는 kgf·cm/cm 이고, 유동성은 ASTM D-1238 시험 방법에 의해 200 ℃, 5 ㎏ 하중의 조건에서 평가하였으며, 단위는 g/10min 이다.Impact strength measurements were evaluated for 1/4 inch thickness by ASTM D-256 test method, unit was kgf · cm / cm, and fluidity was evaluated under conditions of 200 ° C and 5 kg load by ASTM D-1238 test method. The unit is g / 10 min.

또한, 내후성은 ASTM D-4459 시험법에 의거 안료나 염료 등이 첨가되지 않은 자연색상의 표준시편과 제논아크로 300시간 조사한 시편과의 색차(dE)를 색차계를 이용하여 측정하였고, 난연성 측정은 UL-94 난연도 판정시험 방법에 따라 1/16 인 치 두께에 대해서 시험하여 판정하였다.In addition, the weather resistance was measured by the color difference meter (dE) between the standard specimen of natural color without the addition of pigments or dyes and the specimen irradiated with xenon arc for 300 hours according to ASTM D-4459 test method. It was determined by testing about 1/16 inch thickness according to the UL-94 flame retardancy determination test method.

[표 2]TABLE 2

Figure 112005078647607-pat00002
Figure 112005078647607-pat00002

상기 표 2의 실시예 및 비교예의 물성비교 결과에서 알 수 있는 바와 같이, ASA 수지, ABS 수지 및 난연제인 할로겐계 화합물로 구성된 본 발명의 난연성 열가소성 수지 조성물이 ASA 수지를 첨가하지 않은 ABS 수지로만 구성된 종래의 수지 조성물에 비하여, 충격강도, 유동성, 내후성, 난연성의 물성이 전체적으로 우수한 것을 알 수 있다. 반면, 비교예 1의 경우 내후성이 현저히 저하되고, 비교예 2의 경우에는 내충격성이 매우 저하되며, 비교예 3은 난연성이 저하됨을 확인할 수 있었다. 상기한 바와 같이, 본 발명에 의한 난연성 열가소성 수지 조성물은 할로겐계 화합물과 산화안티몬을 난연제로 사용하여 ASA 수지의 난연성을 향상시키는 효과가 있다는 사실을 확인할 수 있었다.As can be seen from the physical property comparison results of Examples and Comparative Examples of Table 2, the flame-retardant thermoplastic resin composition of the present invention composed of an ASA resin, an ABS resin, and a halogen-based compound that is a flame retardant is composed only of an ABS resin to which no ASA resin is added Compared with the conventional resin composition, it can be seen that the physical properties of impact strength, fluidity, weather resistance, and flame retardancy are excellent overall. On the other hand, in the case of Comparative Example 1, the weather resistance is remarkably lowered, in the case of Comparative Example 2, the impact resistance is very low, and Comparative Example 3 was confirmed that the flame retardancy is lowered. As described above, it was confirmed that the flame retardant thermoplastic resin composition according to the present invention has an effect of improving the flame retardancy of the ASA resin by using a halogen-based compound and antimony oxide as a flame retardant.

본 발명에 의한 난연성 열가소성 수지 조성물은 ASA 수지에 할로겐계 난연제 및 산화안티몬을 병용 사용함으로써, 기계적 물성을 유지하면서, 탁월한 내후성을 보유하면서도 난연성이 우수하다는 잇점을 갖는다.The flame retardant thermoplastic resin composition according to the present invention has the advantage of using flame retardants and antimony oxide in combination with ASA resin, while maintaining mechanical properties and having excellent weather resistance and excellent flame retardancy.

Claims (7)

하기 (A)+(B) : (C)의 중량비가 20∼60 : 40∼80이고, (A) : (B)의 중량비가 50∼90 : 10∼50인 기초 수지 (A)+(B)+(C) 100 중량부에 대하여, Basic resin (A) + (B) whose weight ratio of following (A) + (B) :( C) is 20-60: 40-80, and the weight ratio of (A) :( B) is 50-90: 10-50. ) 100 parts by weight (C), 할로겐계 화합물 5∼30 중량부;5 to 30 parts by weight of a halogen compound; 산화안티몬 1∼15 중량부; 및1 to 15 parts by weight of antimony oxide; And 염소 유기화합물 1∼10 중량부를 포함하는 것을 특징으로 하는 난연성 열가소성 수지 조성물:A flame retardant thermoplastic resin composition comprising 1 to 10 parts by weight of a chlorine organic compound: (A)는 아크릴계 합성고무 30∼60 중량%와 시안화비닐 화합물-방향족비닐 화합물 공중합체 40∼70 중량%로 이루어진 아크릴계 그라프트 중합체 ;(A) is an acrylic graft polymer composed of 30 to 60 wt% of acrylic synthetic rubber and 40 to 70 wt% of a vinyl cyanide compound-aromatic vinyl compound copolymer; (B) 디엔계 합성고무 30∼60 중량%와 시안화비닐 화합물-방향족비닐 화합물 공중합체 40∼70 중량%로 이루어진 디엔계 그라프트 중합체 ;(B) a diene graft polymer composed of 30 to 60 wt% of a diene synthetic rubber and 40 to 70 wt% of a vinyl cyanide compound-aromatic vinyl compound copolymer; (C) 시안화비닐 화합물 20∼40 중량%와 방향족비닐 화합물 60∼80 중량%로 이루어진 시안화비닐 화합물-방향족비닐 화합물 공중합체.(C) Vinyl cyanide compound-aromatic vinyl compound copolymer which consists of 20-40 weight% of vinyl cyanide compounds and 60-80 weight% of aromatic vinyl compounds. 제 1항에 있어서, 상기 (A) 또는 (B)의 시안화비닐 화합물-방향족비닐 화합물 공중합체는 시안화비닐 화합물 20∼30 중량%와 방향족비닐 화합물 70∼80 중량%로 이루어지는 것을 특징으로 하는 난연성 열가소성 수지 조성물.The flame retardant thermoplastic according to claim 1, wherein the vinyl cyanide compound-aromatic vinyl compound copolymer of (A) or (B) comprises 20 to 30% by weight of a vinyl cyanide compound and 70 to 80% by weight of an aromatic vinyl compound. Resin composition. 제 1항에 있어서, 상기 (C)의 시안화비닐 화합물-방향족비닐 화합물 공중합체의 중량평균 분자량이 80,000∼400,000인 것을 특징으로 하는 난연성 열가소성 수지 조성물.The flame-retardant thermoplastic resin composition according to claim 1, wherein the weight average molecular weight of the vinyl cyanide compound-aromatic vinyl compound copolymer of (C) is 80,000 to 400,000. 제 1항 내지 제 3항 중 어느 하나의 항에 있어서, 상기 시안화비닐 화합물은 아크릴로니트릴 및 메타크릴로니트릴로 구성된 군에서 선택된 1종 또는 2종인 것을 특징으로 하는 난연성 열가소성 수지 조성물.The flame retardant thermoplastic resin composition according to any one of claims 1 to 3, wherein the vinyl cyanide compound is one or two selected from the group consisting of acrylonitrile and methacrylonitrile. 제 1항 내지 제 3항 중 어느 하나의 항에 있어서, 상기 방향족비닐 화합물은 스티렌, 알파-메틸스티렌, p-t-부틸스티렌, 2,4-디메틸스티렌 및 비닐톨루엔으로 구성된 군에서 선택된 1종 또는 2종 이상인 것을 특징으로 하는 난연성 열가소성 수지 조성물. The method according to any one of claims 1 to 3, wherein the aromatic vinyl compound is one or two selected from the group consisting of styrene, alpha-methylstyrene, pt-butylstyrene, 2,4-dimethylstyrene and vinyltoluene. Flame retardant thermoplastic resin composition, characterized in that more than. 제 1항에 있어서, 상기 할로겐계 화합물은 테트라브로모비스페놀 A, 비스(트리브로모페녹시)에탄, 브롬화 에폭시 수지, 에폭시 말단이 트리브로모페놀로 치환된 브롬화 에폭시 수지 및 2,4,6-트리(2,4,6-트리브로모페녹시)-1,3,5 트리아진 으로 구성된 군으로부터 선택된 1종 또는 2종 이상인 것을 특징으로 하는 난연성 열가소성 수지 조성물.The method of claim 1, wherein the halogen-based compound is tetrabromobisphenol A, bis (tribromophenoxy) ethane, brominated epoxy resin, a brominated epoxy resin substituted with tribromophenol epoxy terminal and 2,4,6 -Tri- (2,4,6-tribromophenoxy) -1,3,5 triazine, one or more selected from the group consisting of flame retardant thermoplastic resin composition. 제 1항에 있어서, 상기 염소 유기화합물은 염소화 폴리에틸렌(CPE) 및 폴리비닐클로라이드(PVC)로 구성된 군으로부터 선택된 1종 또는 2종인 것을 특징으로 하는 난연성 열가소성 수지 조성물.The flame retardant thermoplastic resin composition of claim 1, wherein the chlorine organic compound is one or two selected from the group consisting of chlorinated polyethylene (CPE) and polyvinyl chloride (PVC).
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KR100932759B1 (en) * 2007-12-28 2009-12-21 제일모직주식회사 Flame retardant thermoplastic resin composition excellent in detergent resistance
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