KR20000038718A - Styrene thermoplastic resin composition excellent in antistatics - Google Patents
Styrene thermoplastic resin composition excellent in antistatics Download PDFInfo
- Publication number
- KR20000038718A KR20000038718A KR1019980053799A KR19980053799A KR20000038718A KR 20000038718 A KR20000038718 A KR 20000038718A KR 1019980053799 A KR1019980053799 A KR 1019980053799A KR 19980053799 A KR19980053799 A KR 19980053799A KR 20000038718 A KR20000038718 A KR 20000038718A
- Authority
- KR
- South Korea
- Prior art keywords
- weight
- parts
- pts
- rubber
- resin composition
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions 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
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/08—Copolymers of styrene
- C08L25/10—Copolymers of styrene with conjugated dienes
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
본 발명은 스티렌계 열가소성 수지 조성물에 관한 것으로, 보다 상세하게는 고무변성된 스티렌 수지에 음이온 계면활성제 혼합물, 글리세릴모노 스테아레이트, 이산화티탄 및 징크-스테아레이트를 포함하는 대전방지성이 우수한 반도체 부품 트레이용 스티렌계 열가소성 수지 조성물에 관한 것이다.The present invention relates to a styrene-based thermoplastic resin composition, and more particularly, to an antistatic semiconductor component comprising an anionic surfactant mixture, glyceryl monostearate, titanium dioxide and zinc-stearate in a rubber-modified styrene resin It relates to a tray styrene-based thermoplastic resin composition.
일반적으로 스티렌 중합체는 경질 투명수지로 무색투명하고 착색이 용이하여 다양한 용도로 사용될 수 있는 열가소성 수지인 반면에 내충격성이 낮은 결점을 갖고 있다. 이러한 문제점을 해결하기 위하여 고무상 물질의 존재하에서 스티렌을 중합하여 충격강도를 높인 내충격성 폴리스티렌(HIPS)을 제조하는 방법이 널리 사용되고 있으며, 이렇게 제조된 고무변성된 스티렌계 수지는 식품용기 및 전기, 전자제품의 부품으로 널리 사용되고 있다.In general, the styrene polymer is a transparent resin that is colorless, transparent and easy to color and can be used for various purposes, while having a low impact resistance. In order to solve this problem, a method of manufacturing impact-resistant polystyrene (HIPS) having high impact strength by polymerizing styrene in the presence of a rubbery material is widely used. The rubber-modified styrene-based resin thus prepared is used in food containers, electrical, It is widely used as a part of electronic products.
그러나, 통상적인 고충격 폴리스티렌 수지의 경우는 대전방지성이 없어 반도체 부품 트레이(Tray)용으로 사용하는 경우 정전기가 발생하여 먼지가 달라붙는 문제점이 있다.However, conventional high-impact polystyrene resins do not have antistatic properties, and when used for a semiconductor component tray (Tray), there is a problem in that static electricity is generated and dust adheres.
본 발명의 목적은 상기와 같은 문제점을 해결하기 위한 것으로, 대전방지성을 부여하기 위하여 고무변성된 스티렌 수지에 음이온 계면활성제 혼합물, 글리세릴모노스테아레이트, 이산화티탄 및 징크-스테아레이트를 첨가함으로써 정전기로 인한 오염을 방지할 수 있는 스티렌계 열가소성 수지 조성물을 제공하는 것이다.An object of the present invention is to solve the above problems, by adding an anionic surfactant mixture, glyceryl monostearate, titanium dioxide and zinc-stearate to the rubber-modified styrene resin to impart antistatic properties It is to provide a styrene-based thermoplastic resin composition that can prevent contamination due to.
즉, 본 발명은 고무변성된 스티렌계 수지 100중량부에 음이온 계면활성제 혼합물 1.0 내지 3.0중량부, 글리세릴모노스테아레이트 0.05 내지 1.0중량부, 이산화티탄 0.3 내지 0.7중량부 및 징크-스테아레이트 0.01 내지 0.1중량부를 포함하는 것을 특징으로 하는 대전방지성이 우수한 스티렌계 열가소성 수지 조성물에 관한 것이다.That is, the present invention is 1.0 to 3.0 parts by weight of the anionic surfactant mixture, 0.05 to 1.0 parts by weight of glyceryl monostearate, 0.3 to 0.7 parts by weight of titanium dioxide and 0.01 to 0.01 parts by weight of the rubber-modified styrene resin It is related with the styrene-type thermoplastic resin composition excellent in the antistatic property characterized by including 0.1 weight part.
이하, 본 발명을 더욱 상세히 설명하면 다음과 같다.Hereinafter, the present invention will be described in more detail.
고무변성된 스티렌계 수지는 모노비닐 방향족 화합물 90 내지 92중량부와 폴리부타디엔계 고무 8 내지 10중량부를 첨가하고 여기에 상온에서 54 내지 76 센티스토크의 점도를 갖는 유동파라핀계 미네랄오일 1.0 내지 2.5중량부 및 산화방지제인 트리에틸렌글리콜-비스-3-(3-t-부틸-4-하이드록시-5-메틸페닐)프로피오네이트[triethyleneglycol-bis-3-(3-t-butyl-4-hydroxy-5-methylphenyl)propionate] 0.05 내지 0.1중량부를 투입하여 열에 의한 괴상연속중합법에 의해 제조되는 것으로 중량평균분자량 19 내지 22만의 범위의 것이다The rubber-modified styrene resin is 90 to 92 parts by weight of a monovinyl aromatic compound and 8 to 10 parts by weight of polybutadiene rubber, and 1.0 to 2.5 parts by weight of liquid paraffinic mineral oil having a viscosity of 54 to 76 centistokes at room temperature. Triethyleneglycol-bis-3- (3-t-butyl-4-hydroxy-), a minor and antioxidant, triethyleneglycol-bis-3- (3-t-butyl-4-hydroxy- 5-methylphenyl) propionate] is prepared by the mass continuous polymerization method by adding 0.05 to 0.1 parts by weight, and has a weight average molecular weight in the range of 19 to 220,000.
바람직한 모노비닐 방향족 화합물로는 스티렌, α-메틸스티렌, α-에틸스티렌, p-메틸스티렌 등을 들 수 있다. 폴리부타디엔계 고무는 1,4-cis 함량이 95중량% 이하이며 전제수지 조성물 100중량부에 대하여 95중량%의 스티렌 모노머 용액에서 용액점도가 25℃에서 20 내지 80센티포아즈 수준으로 폴리스티렌 상에 분산된 고무상 물질의 평균입경은 1.0 내지 3.0미크론의 분포를 갖는 것이 사용된다.Preferred monovinyl aromatic compounds include styrene, α-methylstyrene, α-ethylstyrene, p-methylstyrene and the like. The polybutadiene-based rubber has a 1,4-cis content of not more than 95% by weight and has a solution viscosity of 20 to 80 centipoise at 25 ° C. in a 95% by weight styrene monomer solution based on 100 parts by weight of the total resin composition. The average particle diameter of the dispersed rubbery material is used having a distribution of 1.0 to 3.0 microns.
폴리부타디엔계 고무는 전체 수지 조성물 100중량부에 대하여 8 내지 10중량부로 사용하는 것이 바람직한데, 8중량부 미만인 경우에는 내충격성과 신율이 저하되고, 10중량부를 초과하는 경우에는 내열성과 강성이 저하되어 바람직하지 못하다. 또한, 고무상 물질의 평균입경이 1.0미크론 미만인 경우에는 내충격성이 저하되고, 3.0 미크론을 초과하는 경우에는 표면광택도가 저하되어 바람직하지 못하다.The polybutadiene-based rubber is preferably used in an amount of 8 to 10 parts by weight based on 100 parts by weight of the total resin composition. When it is less than 8 parts by weight, impact resistance and elongation are lowered, and when it exceeds 10 parts by weight, heat resistance and rigidity are decreased. Not desirable Moreover, when the average particle diameter of a rubbery material is less than 1.0 micron, impact resistance falls, and when it exceeds 3.0 microns, surface glossiness falls and it is unpreferable.
미네랄오일은 1.0중량부 미만인 경우에는 유동성이 저하되고, 2.5중량부를 초과하는 경우에는 내열성이 떨어진다.If the mineral oil is less than 1.0 parts by weight, the fluidity is lowered, and if it is more than 2.5 parts by weight, the heat resistance is inferior.
최종 중합물의 중량평균분자량은 중합온도, 반응기중량을 조절하여 19만 내지 22만이 되도록 하는 것이 바람직한데, 중량평균분자량이 19만 미만인 경우에는 강성이 떨어지고 22만을 초과하는 경우에는 유동성이 저하되어 바람직하지 못하다.The weight average molecular weight of the final polymer is preferably adjusted to only 190,000 to 22 by adjusting the polymerization temperature and the reactor weight. When the weight average molecular weight is less than 190,000, the rigidity is lowered. Can not do it.
고무변성된 스티렌계 수지의 중합법으로는 괴상연속중합법으로 중합하는 것이 바람직한데, 이는 괴상연속중합법에 의할 경우 대량생산으로 제조원가가 저렴해지고 균일한 물성을 갖는 제품을 생산하기 쉽기 때문이다.Polymerization of rubber-modified styrene-based resins is preferably carried out by a bulk continuous polymerization method, since the bulk continuous polymerization method makes it easy to produce a product with low production cost and uniform properties by mass production. .
이상에서와 같이 제조된 고무변성된 스티렌계 수지에 첨가되는 음이온계면활성제 혼합물은 황염소화되고 수산화나트륨으로 비누화된 파라핀오릴과 마그네슘염성분으로 되어 있고, 사용량은 1.0 내지 3.0 중량부가 바람직하다. 음이온계면활성제 혼합물의 사용량이 1.0중량부 미만인 경우에는 대전방지성(대전압반감기, 표면저항)이 불량해지고, 3.0중량부를 초과하는 경우에는 성형품에 박리현상이 발생되어 바람직하지 못하다.The anionic surfactant mixture added to the rubber-modified styrene resin prepared as described above is composed of paraffin oryl and magnesium salts sulphated and saponified with sodium hydroxide, and the amount is preferably 1.0 to 3.0 parts by weight. If the amount of the anionic surfactant mixture is less than 1.0 part by weight, the antistatic property (large voltage half-life, surface resistance) is poor, and if it exceeds 3.0 parts by weight, peeling occurs in the molded article, which is not preferable.
본 발명에서 사용된 글리세릴 모노스테아레이트는 55 내지 70℃의 융점 범위 를 갖고 80℃에서 벌크덴시티(bulk density)가 0.890 내지 0.896범위를 갖는 것으로 0.05 내지 1.0중량부가 사용된다. 글리세릴 모노스테아레이트의 사용량이 0.05중량부 미만인 경우에는 대전방지성이 나빠지고, 1.0중량부를 초과하는 경우에는 성형물표면에 가스자국이 생겨 바람직하지 못하다.Glyceryl monostearate used in the present invention has a melting point range of 55 to 70 ℃ and a bulk density at 0.8 ℃ to have a range of 0.890 to 0.896 is used 0.05 to 1.0 parts by weight. If the amount of the glyceryl monostearate is less than 0.05 part by weight, the antistatic property is worsened. If the amount of the glyceryl monostearate is less than 1.0 part by weight, gas traces are formed on the surface of the molding, which is not preferable.
징크-스테아레이트는 고급지방산의 금속염으로 0.01 내지 0.1중량부가 사용되고, 이산화티탄은 비중이 4.2인 백색분말의 형상을 갖는 것이 사용된다. 징크스테아레이트 및 이산화티탄의 함량이 각각 0.01중량부 및 0.3중량부 미만으로 사용되면 대전방지성이 급격히 저하되고, 0.1중량부 및 0.7중량부를 초과하여 사용하여도 대전방지성은 더 이상 향상되지 않으므로 본 발명의 범위내로 사용하는 것이 가장 바람직하다.Zinc-stearate is used as a metal salt of higher fatty acids, 0.01 to 0.1 parts by weight, and titanium dioxide is used having a shape of a white powder having a specific gravity of 4.2. When the content of zinc stearate and titanium dioxide is less than 0.01 parts by weight and 0.3 parts by weight, respectively, the antistatic property is drastically reduced, and even when used in excess of 0.1 part and 0.7 parts by weight, the antistatic property is no longer improved. Most preferably used within the scope of the invention.
이하, 본 발명은 실시예를 들어 더욱 자세히 설명하고자 하나 본 발명이 하기 실시예에 의하여 제한되는 것은 아니다.Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited by the following Examples.
제조실시예 : 고무변성된 스티렌계 수지Preparation Example: Rubber-Modified Styrene Resin
스티렌 90.5중량부에 폴리부타디엔계 고무 9.5중량부, 상온에서 54 내지 76센티스토크의 점도를 갖는 유동파라핀계 미네랄오일 2.0중량부, 산화방지제인 트리에틸렌글리콜비스-3-(3-t-부틸-4-하이드록시-5-메틸페닐)프로피오네이트 0.05중량부를 투입하여 열에 의한 괴상연속중합법에 의해 중량평균분자량이 21만인 스티렌계 열가소성 수지를 제조하였다.9.5 parts by weight of styrene, 9.5 parts by weight of polybutadiene rubber, 2.0 parts by weight of liquid paraffinic mineral oil having a viscosity of 54 to 76 centistokes at room temperature, triethylene glycol bis-3- (3-t-butyl- as an antioxidant 0.05 weight part of 4-hydroxy-5-methylphenyl) propionate was prepared, and the styrenic thermoplastic resin having a weight average molecular weight of 210,000 was prepared by thermal bulk polymerization.
상기에서 사용된 폴리부타디엔 고무는 1,4-cis 함량이 95중량% 이하이며 전체수지 조성물 100중량부에 대하여 95중량%의 스티렌 모노머 용액에서 용액점도가 25℃에서 55센티포아즈 수준인 폴리부타디엔계 고무이고, 폴리스티렌상에 분산된 각 고무상 물질의 평균입경은 2.0미크론의 분포를 가진 것이다.The polybutadiene rubber used above has a 1,4-cis content of not more than 95% by weight and polybutadiene having a solution viscosity of 55 centipoise at 25 ° C. in a 95% by weight styrene monomer solution based on 100 parts by weight of the total resin composition. It is a type | system | group rubber | gum and the average particle diameter of each rubbery material disperse | distributed on polystyrene has a distribution of 2.0 micron.
실시예 1Example 1
제조실시예에 의하여 제조된 고무변성된 스티렌계 수지 100중량부, 글리세릴모노스테아레이트 1.0중량부, 이산화티탄 0.7중량부, 징크-스테아레이트 0.05중량부를 첨가하여 헨셀믹서에서 10분간 블랜드한 후 온도 190 내지 230℃, 스크류 210rpm 조건하에서 이축혼련 압출기를 사용하여 펠렛화하여 사출성형기로 테스트 시편을 제작한 후 다음의 조건으로 대전방지성을 측정하였다.100 parts by weight of the rubber-modified styrene resin prepared by the Preparation Example, 1.0 part by weight of glyceryl monostearate, 0.7 parts by weight of titanium dioxide, 0.05 parts by weight of zinc-stearate were blended in a Henschel mixer for 10 minutes Pelletization was carried out using a twin screw kneading extruder under conditions of 190 to 230 ° C and a screw 210rpm to produce a test specimen using an injection molding machine, and then the antistatic property was measured under the following conditions.
대전방지성 평가Antistatic evaluation
(1)대전압반감기 : 온도 23℃, 상대습도 50%, 인가전압 8kv, 인가시간 60초(1) Large voltage half life: temperature 23 ℃, relative humidity 50%, applied voltage 8kv, applied time 60 seconds
(2)표면저항 : 온도 23℃, 상대습도 50%, 인가전압 500V, 측정시간 30sec(2) Surface resistance: temperature 23 ℃, relative humidity 50%, applied voltage 500V, measurement time 30sec
실시예 2Example 2
고무변성된 스티렌 수지 100중량부, 음이온 계면활성제 혼합물 3.0중량부, 글리세릴모노스테아레이트 0.05중량부, 이산화티탄 0.3중량부, 징크-스테아레이트 0.01중량부를 첨가하여 실시예 1과 같은 방법으로 제조하였다.100 parts by weight of a rubber-modified styrene resin, 3.0 parts by weight of anionic surfactant mixture, 0.05 parts by weight of glyceryl monostearate, 0.3 parts by weight of titanium dioxide, and 0.01 parts by weight of zinc-stearate were added in the same manner as in Example 1. .
실시예 3Example 3
고무변성된 스티렌계 수지 100중량부, 음이온 계면활성제 혼합물 2.0중량부, 글리세릴 모노스테아레이트 0.5중량부, 이산화티탄 0.5중량부, 징크-스테아레이트 0.1중량부를 첨가하여 실시예 1과 동일한 방법으로 제조하였다.Prepared in the same manner as in Example 1 by adding 100 parts by weight of the rubber-modified styrene resin, 2.0 parts by weight of anionic surfactant mixture, 0.5 parts by weight of glyceryl monostearate, 0.5 parts by weight of titanium dioxide, 0.1 parts by weight of zinc-stearate It was.
비교예 1Comparative Example 1
고무변성된 스티렌계 수지 100중량부, 음이온 계면활성제 혼합물 2.0중량부, 글리세릴 모노스테아레이트 0.2중량부, 이산화티탄 0.5중량부를 첨가하여 실시예 1과 동일한 방법으로 제조하였다.100 parts by weight of a rubber-modified styrene resin, 2.0 parts by weight of anionic surfactant mixture, 0.2 parts by weight of glyceryl monostearate, and 0.5 parts by weight of titanium dioxide were added to prepare the same method as in Example 1.
비교예 2Comparative Example 2
고무변성된 스티렌계수지 100중량부, 음이온 계면활성제 혼합물 0.8중량부, 징크-스테아레이트 0.2중량부, 이산화티탄 1.0중량부를 첨가하여 실시예 1과 동일한 방법으로 제조하였다.100 parts by weight of rubber-modified styrene resin, 0.8 parts by weight of anionic surfactant mixture, 0.2 parts by weight of zinc-stearate, and 1.0 parts by weight of titanium dioxide were added to prepare the same method as in Example 1.
비교예 3Comparative Example 3
고무변성된 스티렌계 수지 100중량부에 음이온 계면활성제 혼합물 0.5중량부, 글리세릴 모노스테아레이트 1.0중량부, 징크-스테아레이트 0.02중량부를 첨가하여 실시예 1과 동일한 방법으로 제조하였다.To 100 parts by weight of the rubber-modified styrene resin, 0.5 part by weight of anionic surfactant mixture, 1.0 part by weight of glyceryl monostearate, and 0.02 part by weight of zinc-stearate were added to prepare the same method as in Example 1.
상기 실시예 및 비교예의 스티렌계 열가소성 수지의 성분 및 물성을 표 1에 나타내었다.Table 1 shows the components and physical properties of the styrene-based thermoplastic resins of Examples and Comparative Examples.
(단위 : 중량부)(Unit: parts by weight)
이상에서 살펴본 바와 같이 본 발명의 고무변성된 스티렌계 수지에 음이온계면활성제, 글리세릴모노스테아레이트, 징크스테아레이트 및 이산화티탄을 첨가한 스티렌계 수지는 대전방지성이 우수하여 정전기방지가 절대적으로 요구되는 반도체부품 트레이용으로 유용하게 사용될 수 있다.As described above, the styrene-based resin in which the anionic surfactant, glyceryl monostearate, zinc stearate, and titanium dioxide is added to the rubber-modified styrene-based resin of the present invention is excellent in antistatic properties and absolutely requires antistatic. It can be usefully used for the semiconductor component tray.
Claims (3)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-1998-0053799A KR100394059B1 (en) | 1998-12-08 | 1998-12-08 | Styrene-based thermoplastic resin composition excellent in antistatic properties |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-1998-0053799A KR100394059B1 (en) | 1998-12-08 | 1998-12-08 | Styrene-based thermoplastic resin composition excellent in antistatic properties |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20000038718A true KR20000038718A (en) | 2000-07-05 |
KR100394059B1 KR100394059B1 (en) | 2003-09-19 |
Family
ID=19561930
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR10-1998-0053799A KR100394059B1 (en) | 1998-12-08 | 1998-12-08 | Styrene-based thermoplastic resin composition excellent in antistatic properties |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR100394059B1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100413355B1 (en) * | 1998-07-21 | 2004-03-30 | 제일모직주식회사 | Styrene-based plastic resin composition with excellent antistatic property and surface gloss |
KR100714905B1 (en) * | 2005-12-29 | 2007-05-04 | 제일모직주식회사 | Thermoplastic resin composition with good wetproof property and transparency |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4131592A (en) * | 1976-10-29 | 1978-12-26 | The R.C.A. Rubber Company | Flame retardant rubber flooring composition |
KR100186725B1 (en) * | 1996-05-22 | 1999-05-15 | 유현식 | Thermoplastic composition having excellent high-impact and paper touch property combined with elongation |
JPH1036464A (en) * | 1996-05-24 | 1998-02-10 | Denki Kagaku Kogyo Kk | Rubber-modified styrene resin and its composition |
KR100198732B1 (en) * | 1997-06-30 | 1999-06-15 | 유현식 | Stylenic thermoplastic resin composition with high anti-static |
-
1998
- 1998-12-08 KR KR10-1998-0053799A patent/KR100394059B1/en not_active IP Right Cessation
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100413355B1 (en) * | 1998-07-21 | 2004-03-30 | 제일모직주식회사 | Styrene-based plastic resin composition with excellent antistatic property and surface gloss |
KR100714905B1 (en) * | 2005-12-29 | 2007-05-04 | 제일모직주식회사 | Thermoplastic resin composition with good wetproof property and transparency |
Also Published As
Publication number | Publication date |
---|---|
KR100394059B1 (en) | 2003-09-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR100543493B1 (en) | Graft Polymer Moulding Compositions With Reduced Deposit Formation | |
WO2018095189A1 (en) | Polycarbonate composition and method for preparing same | |
WO2018099218A1 (en) | Polycarbonate composition and preparation method therefor | |
KR100394059B1 (en) | Styrene-based thermoplastic resin composition excellent in antistatic properties | |
JP5529572B2 (en) | Rubber-modified styrenic resin composition and sheet and container using the same | |
JPH1053679A (en) | Styrene polymer composition | |
CN113292799A (en) | Transparent PVC-U electrical casing and preparation method thereof | |
CN109983065B (en) | Thermoplastic molding composition comprising a styrene polymer and a lubricant and process for its preparation | |
WO2023160183A1 (en) | Polycarbonate composition, and preparation method therefor and use thereof | |
JPS63289068A (en) | Polyarylene sulfide resin composition | |
KR100198732B1 (en) | Stylenic thermoplastic resin composition with high anti-static | |
KR100413355B1 (en) | Styrene-based plastic resin composition with excellent antistatic property and surface gloss | |
KR20100011561A (en) | Resin composition with an anti-scratch and flame-retardent propeties | |
US3935152A (en) | Styrene-acrylonitrile resin composition having good parting property | |
US2532245A (en) | Thermoplastic compositions with reduced flow viscosity | |
KR20020044387A (en) | Thermoplastic Resin Composition Having Excellent Heat Stability and Ultraviolet Stability | |
US2980640A (en) | Polymeric compositions | |
KR100524321B1 (en) | Styrenic therpoplastic resin composition | |
KR100186725B1 (en) | Thermoplastic composition having excellent high-impact and paper touch property combined with elongation | |
US3932362A (en) | Amorphous polyamide of C-alkyl substituted diamine and terephthalic acid dialkyl ester having improved electrical creep resistance | |
KR19980046810A (en) | Styrene-based thermoplastic resin composition excellent in antistatic properties | |
KR100556619B1 (en) | Thermoplastic Styrene Resin Composition for Gas Assist Injection Molding | |
KR20220045767A (en) | Thermoplastic resin composition, method for preparing the same and molded article therefrom | |
KR20230101487A (en) | Thermoplastic resin composition and molded article using the same | |
JPH1053680A (en) | Styrene polymer composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant | ||
FPAY | Annual fee payment |
Payment date: 20130607 Year of fee payment: 11 |
|
FPAY | Annual fee payment |
Payment date: 20140605 Year of fee payment: 12 |
|
FPAY | Annual fee payment |
Payment date: 20150623 Year of fee payment: 13 |
|
FPAY | Annual fee payment |
Payment date: 20160617 Year of fee payment: 14 |
|
FPAY | Annual fee payment |
Payment date: 20170621 Year of fee payment: 15 |
|
LAPS | Lapse due to unpaid annual fee |