JP2002530504A - Polystyrene resin composition for injection molding - Google Patents

Polystyrene resin composition for injection molding

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Publication number
JP2002530504A
JP2002530504A JP2000584004A JP2000584004A JP2002530504A JP 2002530504 A JP2002530504 A JP 2002530504A JP 2000584004 A JP2000584004 A JP 2000584004A JP 2000584004 A JP2000584004 A JP 2000584004A JP 2002530504 A JP2002530504 A JP 2002530504A
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JP
Japan
Prior art keywords
injection molding
styrene
polystyrene
rubber
composition
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
JP2000584004A
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Japanese (ja)
Inventor
ゼ ソン チョウ
Original Assignee
デーウー・エレクトロニクス・カンパニー・リミテッド
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Publication of JP2002530504A publication Critical patent/JP2002530504A/en
Pending legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F279/00Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
    • C08F279/02Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes
    • 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F291/00Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
    • C08F291/02Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00 on to elastomers
    • 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
    • C08L25/06Polystyrene
    • 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
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group

Abstract

(57)【要約】 本発明は射出成形用ポリスチレン系樹脂組成物に係り、異なる粒子サイズのゴムを含む第1および第2のスチレン組成物の混合物よりなり、第1のスチレン組成物は3〜5μmの粒子径を有するゴムを6〜8%含み、第2のスチレン組成物は1〜3μmの粒子径を有するゴムを7〜9%含む。これにより、射出成形後大きいサイズのゴム粒子と小さなサイズのゴム粒子が互い密接に接触するようになって、溶接ラインの発生を抑えて成形品の外観特性を向上させることができる。   (57) [Summary] The present invention relates to a polystyrene resin composition for injection molding, comprising a mixture of first and second styrene compositions containing rubbers of different particle sizes, wherein the first styrene composition has a particle diameter of 3 to 5 μm. The second styrene composition contains 6 to 8% of rubber and 7 to 9% of rubber having a particle size of 1 to 3 μm. As a result, the rubber particles having a large size and the rubber particles having a small size come into intimate contact with each other after the injection molding, so that the appearance of a molded product can be improved by suppressing the occurrence of a welding line.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】 (技術分野) 本発明は射出成形用ポリスチレン系樹脂組成物に係り、とくに射出成形する際
に形成される溶接ラインのような外形上の欠陥を減らして塗装処理のような後処
理工程を省くための射出成形用ポリスチレン系樹脂組成物に関する。
TECHNICAL FIELD [0001] The present invention relates to a polystyrene resin composition for injection molding, and more particularly to a post-processing step such as a coating process by reducing external defects such as a welding line formed during injection molding. The present invention relates to a polystyrene-based resin composition for injection molding for omitting the above.

【0002】 (背景技術) 一般に、ポリスチレンは有機過酸化物(organic peroxide)
などの開始剤(initiator)を使用したスチレンのラジカル重合により
生成される。
BACKGROUND ART In general, polystyrene is an organic peroxide.
It is produced by radical polymerization of styrene using an initiator such as.

【0003】 こうして得られるポリスチレンは、直鎖構造を有し、透明性に優れ比重が小さ
く、電気および高周波絶縁性に優れた特性を有しているが、軟化温度が低く、固
くて壊れ易いという欠点がある。
[0003] The polystyrene thus obtained has a linear structure, is excellent in transparency, has a low specific gravity, and has excellent properties in electrical and high-frequency insulation. However, it has a low softening temperature and is hard and easily broken. There are drawbacks.

【0004】 ポリスチレン系樹脂は比較的低い温度領域で低い融点粘度を持ち、温度低下に
伴う粘度の減少程度が緩慢であり、成形温度範囲が広く、透明性と成形特性が優
れている。
[0004] Polystyrene resins have a low melting point viscosity in a relatively low temperature range, the degree of viscosity decrease with temperature decrease is slow, the molding temperature range is wide, and transparency and molding characteristics are excellent.

【0005】 したがって、家庭用電気、電子製品向けケースには高衝撃性ポリスチレン(H
igh Impact PS)樹脂とABS樹脂が広く使われている。高衝撃性
ポリスチレン(HIPS)樹脂はスチレンを重合した汎用のポリスチレン(Ge
neral Purpose PS)樹脂に合成ゴム5〜20%を配合して得ら
れ、これによってポリスチレンの壊れ易い点を改善したものであり、ABS樹脂
はアクリロニトリル、ブタジエン、スチレンの3つの成分よりなる耐衝撃性熱可
塑性樹脂である。
[0005] Therefore, high impact polystyrene (H
(High Impact PS) resin and ABS resin are widely used. High impact polystyrene (HIPS) resin is a general-purpose polystyrene (Ge
Neural Purpose PS) resin is obtained by compounding 5 to 20% of synthetic rubber, thereby improving the fragility of polystyrene. It is a thermoplastic resin.

【0006】 このような各樹脂の流動長さLと成形品のビルディング厚さ(buildin
g thickness)tの比(L/t)は汎用ポリスチレン(GPPS)樹
脂が230〜250、高衝撃性ポリスチレン(HIPS)樹脂が220〜230
、ABS樹脂が190〜200である。
The flow length L of each resin and the building thickness of a molded product (buildin)
The ratio (L / t) of gthickness / t is 230-250 for general-purpose polystyrene (GPPS) resin and 220-230 for high-impact polystyrene (HIPS) resin.
, ABS resin is 190 to 200.

【0007】 したがって、樹脂の流動性はABS樹脂、GPPS樹脂、HIPS樹脂の順に
優れているが、ABS樹脂の価格が汎用ポリスチレン(GPPS)樹脂や高衝撃
性ポリスチレン(HIPS)樹脂より高価なので、テレビビジョンケースのよう
な一般家電製品には高衝撃性ポリスチレン(HIPS)樹脂が広く使われている
Accordingly, although the fluidity of the resin is superior in the order of the ABS resin, the GPPS resin, and the HIPS resin, the price of the ABS resin is higher than that of the general-purpose polystyrene (GPPS) resin or the high-impact polystyrene (HIPS) resin. High impact polystyrene (HIPS) resin is widely used for general home appliances such as a vision case.

【0008】 しかし、HIPS樹脂は流動性に劣るため、射出成形時に成形品に溶接ライン
が生じ、射出成形後別の後加工処理として塗装処理を施さなければならなくなる
However, since the HIPS resin is inferior in fluidity, a welding line is formed in a molded product at the time of injection molding, and a coating process must be performed as another post-processing process after the injection molding.

【0009】 溶接ラインとは、金型内で二つの分岐溶融された樹脂が合流する部分に細い実
線で形成されることを指す。溶接ラインが生ずる主な原因は、二つの樹脂の前端
部における低い温度によって、二つの分岐溶融された樹脂が合流地点で完全に混
合できないからであり、樹脂に含まれた水分や揮発成分あるいは射出成形中使用
する離型剤によっても溶接ラインが生じる場合がある。
The term “welding line” means that a thin solid line is formed at a portion where two branched and fused resins meet in a mold. The main cause of the welding line is that the low temperature at the front end of the two resins makes it impossible for the two branched and melted resins to be completely mixed at the confluence point. A welding line may also be formed depending on the release agent used during molding.

【0010】 射出成形を施すためには樹脂を通過させるゲートを必要とする。成形品が大き
い場合や複雑になる場合は二つ以上のゲートを必要とするが、この場合に溶接ラ
インが形成されやすい。一方、一つのゲートに溶融樹脂が供給されるとしても、
成形品内にインサート部品またはホールがある場合や成形品のビルディング厚さ
が違う場合も溶接ラインが生ずる。
[0010] Injection molding requires a gate through which resin passes. When a molded product is large or complicated, two or more gates are required. In this case, a welding line is easily formed. On the other hand, even if molten resin is supplied to one gate,
Weld lines also occur when there are inserts or holes in the part or when the building thickness of the part is different.

【0011】 図1の(a)および(b)は溶接ラインの形成過程を説明するための模式図で
あって、図1(a)に示すように、溶融樹脂は二つのゲート12,14を通って
キャビティ内に供給され、樹脂の二つの分岐された部分が合流する部分に溶接ラ
インが形成される。
FIGS. 1A and 1B are schematic views for explaining a process of forming a welding line. As shown in FIG. 1A, a molten resin forms two gates 12 and 14. The welding line is formed at a portion where the two branched portions of the resin are fed into the cavity and merge.

【0012】 このとき、分岐溶融された樹脂が合流されてもゲート12,14と近接した部
位では溶接ラインが形成されず、ゲート12,14から遠く離れた部位に溶接ラ
インが形成されるが、これは二つのゲート12,14から離れた部位では、金型
を通じて冷却され低い温度になった溶融樹脂が完全に融合できなくなって溶接ラ
イン16が形成されることによる。
At this time, even if the branched and molten resins are merged, a welding line is not formed in a portion close to the gates 12 and 14, and a welding line is formed in a portion far away from the gates 12 and 14. This is because, at a position apart from the two gates 12 and 14, the molten resin cooled through the mold and cooled to a low temperature cannot be completely fused, and the welding line 16 is formed.

【0013】 一方、図1(b)に示すように、成形品の内部にホール18がある場合は、一
つのゲート12を通じて溶融樹脂が供給されても、溶融樹脂がホール18の周囲
で分岐され、その後再び合流するときに溶接ライン16が形成される。
On the other hand, as shown in FIG. 1B, when there is a hole 18 inside the molded product, even if the molten resin is supplied through one gate 12, the molten resin is branched around the hole 18. Thereafter, when they merge again, a welding line 16 is formed.

【0014】 このような溶接ラインは、HIPS樹脂に衝撃性と流動性を向上させるために
ブタジエンを含有させた場合に、流動性の低下によって必然的に発生するように
なることであって、このような溶接ラインは成形品の強度を低下させるだけでな
く、成形品の外観品質水準を低下させることになるので、射出工程が終わった後
に溶接ラインを見えなくするために塗装作業を施さなければならなかった。
[0014] Such a welding line is inevitably generated due to a decrease in fluidity when butadiene is added to the HIPS resin in order to improve impact strength and fluidity. Such a welding line not only reduces the strength of the molded product, but also lowers the appearance quality level of the molded product, so it is necessary to perform painting work to make the welding line invisible after the injection process did not become.

【0015】 (発明の開示) 本発明は前述の問題点を解決するために案出されたもので、樹脂組成物の溶融
時の流動性を高めて、射出成形時の溶接ラインの発生を最小化させる射出成形用
ポリスチレン系樹脂組成物を提供することを目的とする。
DISCLOSURE OF THE INVENTION [0015] The present invention has been devised to solve the above-described problems, and enhances the fluidity of a resin composition during melting to minimize the occurrence of a welding line during injection molding. It is an object of the present invention to provide a polystyrene resin composition for injection molding to be converted.

【0016】 前記目的を達成するための本発明に係る射出成形用ポリスチレン系樹脂組成物
は、異なる粒子サイズのゴムを含む第1および第2のスチレン組成物を混合して
なることを特徴とする。
The polystyrene resin composition for injection molding according to the present invention for achieving the above object is characterized by mixing first and second styrene compositions containing rubbers having different particle sizes. .

【0017】 ここで、第1スチレン組成物は3〜5μmの粒子径を有するゴムを6〜8%含
むものであり、第2スチレン組成物は1〜3μmの粒子径を有するゴムを7〜9
%含むものであることが望ましい。
Here, the first styrene composition contains 6 to 8% of a rubber having a particle diameter of 3 to 5 μm, and the second styrene composition contains a rubber of 7 to 9 having a particle diameter of 1 to 3 μm.
%.

【0018】 さらに、前記ポリスチレン系樹脂組成物は、第1スチレン組成物を70〜90
%と第2スチレン組成物を9〜29%および熱安定剤とシリコンオイルを含むも
のであることが望ましい。
Further, the polystyrene-based resin composition may contain the first styrene composition in an amount of 70 to 90.
% And 9 to 29% of the second styrene composition, and a heat stabilizer and silicone oil.

【0019】 本発明によれば、異なる粒子サイズのゴムを含むスチレン組成物を混合するこ
とにより、流動性特性を改善し、その結果、溶接ラインの発生を抑えて成形品の
外観特性を向上させることができる。
According to the present invention, by mixing styrene compositions containing rubbers of different particle sizes, the fluidity characteristics are improved, and as a result, the appearance of a molded product is improved by suppressing the occurrence of welding lines. be able to.

【0020】 (発明を実施するための最良の形態) 以下、添付した図面を参照して本発明の実施形態を説明する。 一般に、ポリスチレン樹脂に合成ゴムの粒子を含ませる場合、単純に粒子サイ
ズの大きいゴム粒子のみ、または粒子サイズの小さいゴム粒子のみを使用してい
る。これらゴム粒子は、ポリスチレンの生地内部に存するブタジエンの繊維組織
に散在し、成形品に衝撃が加わればこの繊維組織に応力が集中しながら微細なク
レージング(crazing)が発生するようになり、クレージングを通じて衝
撃が吸収できる。
Hereinafter, embodiments of the present invention will be described with reference to the accompanying drawings. Generally, when synthetic rubber particles are included in a polystyrene resin, only rubber particles having a large particle size or rubber particles having a small particle size are simply used. These rubber particles are scattered in the fiber structure of butadiene existing inside the polystyrene cloth, and when an impact is applied to the molded product, stress is concentrated on the fiber structure, and fine crazing (crazing) occurs. Shock can be absorbed.

【0021】 しかし、ポリスチレンに含ませるゴム粒子として粒子サイズの大きいゴム粒子
または粒子サイズの小さいゴム粒子を大量に使用した場合は、射出成形時の流動
性はゴム粒子の使用量に比例するようになる。
However, when a large amount of rubber particles having a large particle size or a small particle size are used as the rubber particles contained in the polystyrene, the fluidity at the time of injection molding should be proportional to the amount of the rubber particles used. Become.

【0022】 したがって、ゴム粒子の使用量をできるだけ少なくして、耐衝撃性を強化させ
ることが必要となる。ポリスチレンに含ませるゴム粒子として粒子のサイズの大
きいものと小さいもののいずれか一種だけを使用した場合は、ゴム粒子をポリス
チレンに均一に分布させることが難しくなる。
Therefore, it is necessary to reduce the amount of rubber particles used as much as possible to enhance the impact resistance. If only one of the large and small rubber particles is used as the rubber particles contained in the polystyrene, it becomes difficult to uniformly distribute the rubber particles in the polystyrene.

【0023】 これに対し、粒子サイズが大きいゴム粒子と粒子サイズが小さいゴム粒子の両
方を使用した場合は、ゴム粒子が均一に混合され、ポリスチレンの耐衝撃性と流
動性の両方を満足させることができる。これによって、射出成形時の成形性が改
善され、成形品の外観特性が向上する。
On the other hand, when both the rubber particles having a large particle size and the rubber particles having a small particle size are used, the rubber particles are uniformly mixed, and both the impact resistance and the fluidity of polystyrene are satisfied. Can be. Thereby, the moldability at the time of injection molding is improved, and the appearance characteristics of the molded product are improved.

【0024】 以下、次の望ましい実施例に基づき本発明を詳細に説明する。 1.実施例1〜5 第1スチレン組成物にはスチレンに平均粒子径が3〜5μmのゴム7%を配合
し、第2スチレン組成物にはスチレンに平均粒子径が1〜2μmのゴム8%を配
合した。この第1および第2スチレン組成物と他の添加物を表1に示す配合比に
よって混合した。
Hereinafter, the present invention will be described in detail with reference to the following preferred embodiments. 1. Examples 1 to 5 In the first styrene composition, 7% of rubber having an average particle diameter of 3 to 5 μm was blended with styrene, and in the second styrene composition, 8% of rubber having an average particle diameter of 1 to 2 μm was mixed with styrene. Was blended. The first and second styrene compositions and other additives were mixed at the mixing ratio shown in Table 1.

【0025】 この混合組成物を射出機シリンダー温度190〜220℃、金型温度50℃、
射出圧力100トンの条件下で射出成形して試験片を製作した。これら試験片の
サイズは450mm×250mmであって、図1(b)に示す中央にインサート
ホール18が形成された金型に一つのゲートを利用して溶融充填された。
[0025] The mixed composition was heated at an injection machine cylinder temperature of 190 to 220 ° C, a mold temperature of 50 ° C,
A test piece was manufactured by injection molding under the conditions of an injection pressure of 100 tons. These test pieces had a size of 450 mm × 250 mm, and were melt-filled using a single gate in a mold having an insert hole 18 formed at the center shown in FIG. 1B.

【0026】[0026]

【表1】 [Table 1]

【0027】 実施例1において、ポリスチレン系樹脂組成物は第1スチレン組成物のみを使
用して得られ、実施例2ないし5においてポリスチレン系樹脂組成物は第2スチ
レン組成物の含有量を少しずつ増やして得られる。ここで、異なる粒子サイズの
ゴムを含むスチレン組成物の配合比率を増やすことにより架橋度(cross
linking ratio)が増加するにつれ、膨張指数が減少することがわ
かる。異なる配合比率で二つの組成物を使用して、図1(b)に示した形状に製
作した試験片に対するテスト結果を表2に示す。
In Example 1, the polystyrene resin composition was obtained by using only the first styrene composition. In Examples 2 to 5, the polystyrene resin composition gradually reduced the content of the second styrene composition. Obtained by increasing. Here, by increasing the mixing ratio of the styrene composition containing rubbers having different particle sizes, the degree of crosslinking (cross) was increased.
It can be seen that the expansion index decreases as the linking ratio increases. Table 2 shows test results for test pieces manufactured using the two compositions at different compounding ratios and having the shape shown in FIG. 1 (b).

【0028】[0028]

【表2】 [Table 2]

【0029】 実施例1では、溶接ラインの長さが長く、幅が広く現れる。第2スチレン組成
物を含む実施例2ないし5では、溶接ラインの長さと幅が減少しているが、第2
スチレン組成物が多量含まれた実施例5は溶接ラインの幅が再び広くなる。そし
て光沢特性は、実施例1より実施例2ないし実施例5が良好となる。むら特性は
、第2スチレン組成物が多量含まれた実施例5は良くなかった。ガス発生量は、
試験片を230℃で30分間滞留させた後に測定した試験片の重量減量で表し、
実施例2および実施例3においてガス発生量は少なくなっている。
In the first embodiment, the welding line has a long length and a wide width. In Examples 2 to 5 including the second styrene composition, the length and width of the welding line were reduced,
In Example 5, in which a large amount of the styrene composition was included, the width of the welding line was widened again. The gloss characteristics of Examples 2 to 5 are better than those of Example 1. The unevenness characteristics of Example 5 containing a large amount of the second styrene composition were not good. The amount of gas generated is
Expressed by the weight loss of the test piece measured after allowing the test piece to stay at 230 ° C. for 30 minutes,
In Example 2 and Example 3, the amount of generated gas was small.

【0030】 以上の実施例からわかるように、粒子サイズが大きいゴムを含んだ第1スチレ
ン組成物と粒子サイズが小さいゴムを含んだ第2スチレン組成物を所定割合で混
合した組成物を用いることにより、射出成形時の成形品の外観品質を改善するこ
とができる。
As can be seen from the above examples, a composition in which a first styrene composition containing a rubber having a large particle size and a second styrene composition containing a rubber having a small particle size are mixed at a predetermined ratio is used. Thereby, the appearance quality of the molded article at the time of injection molding can be improved.

【0031】 前記実施例では第1および第2のポリスチレン組成物を単純に混合するだけと
誤解される恐れがあるが、実際にはこれらを混合した後射出成形を進行すること
により、粒子サイズが大きいゴムと粒子サイズが小さいゴム粒子が互いに密接に
接触して成形品の外観品質が一層向上されるのである。
In the above embodiment, there is a risk that the first and second polystyrene compositions may be misunderstood simply as being simply mixed. However, in practice, the mixture is mixed and then subjected to injection molding to reduce the particle size. The large rubber and the rubber particles having a small particle size are in close contact with each other, so that the appearance quality of the molded product is further improved.

【0032】 以上述べた通り、本発明は粒子サイズの大きいゴムが含まれたポリスチレン組
成物と粒子サイズが小さいゴムが含まれたポリスチレン組成物を混合して得られ
た組成物を射出成形することにより、成形品の外観を改善する効果がある。
As described above, the present invention relates to injection molding a composition obtained by mixing a polystyrene composition containing a rubber having a large particle size and a polystyrene composition containing a rubber having a small particle size. This has the effect of improving the appearance of the molded article.

【0033】 また、本発明の望ましい実施例について記述したが、本発明はこれに限らず、
請求範囲に記載された本発明の技術的思想及び保護範囲内で当業者により多様な
変更および修正が可能である。
Although the preferred embodiment of the present invention has been described, the present invention is not limited to this.
Various changes and modifications can be made by those skilled in the art without departing from the technical concept and the protection scope of the present invention described in the claims.

【図面の簡単な説明】[Brief description of the drawings]

【図1】 (a)は溶接ラインの形成過程を示す概略図、(b)は溶接ライ
ンの他の形成過程を示す概略図である。
FIG. 1A is a schematic diagram showing a process of forming a welding line, and FIG. 1B is a schematic diagram showing another process of forming a welding line.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) B29K 105:16 B29K 105:16 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) B29K 105: 16 B29K 105: 16

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 異なる粒子サイズのゴムを含む第1および第2のスチレン組
成物を混合してなる射出成形用ポリスチレン系樹脂組成物。
1. A polystyrene resin composition for injection molding obtained by mixing first and second styrene compositions containing rubbers having different particle sizes.
【請求項2】 前記第1のスチレン組成物は3〜5μmの粒子径を有するゴ
ムをA%含むものであり、前記第2のスチレン組成物は1〜3μmの粒子径を有
するゴムをB%含むものである請求項1に記載の射出成形用ポリスチレン系樹脂
組成物。
2. The first styrene composition contains A% of a rubber having a particle diameter of 3 to 5 μm, and the second styrene composition contains B% of a rubber having a particle diameter of 1 to 3 μm. The polystyrene resin composition for injection molding according to claim 1, which comprises:
【請求項3】 前記Aは6〜8であり、前記Bは7〜9である請求項2に記
載の射出成形用ポリスチレン系樹脂組成物。
3. The polystyrene resin composition for injection molding according to claim 2, wherein A is 6 to 8, and B is 7 to 9.
【請求項4】 前記ポリスチレン系樹脂組成物は、前記第1のスチレン組成
物を70〜90%と前記第2のスチレン組成物を9〜29%および熱安定剤とシ
リコンオイルを含むものである請求項2に記載の射出成形用ポリスチレン系樹脂
組成物。
4. The polystyrene-based resin composition contains 70 to 90% of the first styrene composition, 9 to 29% of the second styrene composition, a heat stabilizer and silicone oil. 3. The polystyrene resin composition for injection molding according to 2.
JP2000584004A 1998-11-24 1999-01-04 Polystyrene resin composition for injection molding Pending JP2002530504A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
KR1019980050390A KR100302128B1 (en) 1998-11-24 1998-11-24 Polystyrene resin compound for injection molding
KR1998/50390 1998-11-24
PCT/KR1999/000003 WO2000031182A1 (en) 1998-11-24 1999-01-04 Polystyrene-based resin composition for injection molding

Publications (1)

Publication Number Publication Date
JP2002530504A true JP2002530504A (en) 2002-09-17

Family

ID=19559447

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000584004A Pending JP2002530504A (en) 1998-11-24 1999-01-04 Polystyrene resin composition for injection molding

Country Status (4)

Country Link
EP (1) EP1198514A1 (en)
JP (1) JP2002530504A (en)
KR (1) KR100302128B1 (en)
WO (1) WO2000031182A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6579946B2 (en) 2001-02-02 2003-06-17 Dow Global Technologies Inc. Low-gloss biaxially oriented films comprising vinyl aromatic polymers and substantially non-spherical rubber particles

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3035570A1 (en) * 1980-09-20 1982-05-06 Basf Ag, 6700 Ludwigshafen IMPACT RESISTANT THERMOPLASTIC SHAPE
DE4018230A1 (en) * 1990-06-07 1991-12-12 Basf Ag THERMOPLASTIC MOLDS
US5428106A (en) * 1993-09-02 1995-06-27 The Dow Chemical Company Rubber modified polystyrene

Also Published As

Publication number Publication date
KR100302128B1 (en) 2001-10-29
EP1198514A1 (en) 2002-04-24
WO2000031182A1 (en) 2000-06-02
KR20000033502A (en) 2000-06-15

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