JPH0422178B2 - - Google Patents
Info
- Publication number
- JPH0422178B2 JPH0422178B2 JP59020084A JP2008484A JPH0422178B2 JP H0422178 B2 JPH0422178 B2 JP H0422178B2 JP 59020084 A JP59020084 A JP 59020084A JP 2008484 A JP2008484 A JP 2008484A JP H0422178 B2 JPH0422178 B2 JP H0422178B2
- Authority
- JP
- Japan
- Prior art keywords
- less
- particle size
- rubber
- weight
- dispersed particles
- 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.)
- Expired - Lifetime
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Graft Or Block Polymers (AREA)
Description
本発明は外観、衝撃強度、耐熱性に優れたゴム
変性スチレン系樹脂組成物に関するものである。
従来、高耐熱、高光沢、高衝撃強度を有する樹
脂として、ABS樹脂があり、家庭電気製品、音
響機器、自動車部品等に使用されている。最近、
これら用途のコストダウン指向が高まり、より安
価なゴム変性スチレン系樹脂に代替する傾向が強
くなつている。代替時、ゴム変性スチレン系樹脂
にABS樹脂が有する物性(耐熱性、外観特性、
衝撃強度)を附与することが要請されている。
従来のゴム変性スチレン系樹脂の外観特性と衝
撃強度のバランス改良はゴム状弾性体の平均粒子
径を制御することにより、改善されてはいるが、
市場要求を充分満足させるにはいたつていない。
又、耐熱性は、未反応モノマー、オリゴマー等を
可能な限り除去しても加熱変形温度で83〜84℃が
限界であり、市場要求の87〜90℃は達成され得な
い。
本発明はα−メチルスチレンを導入し、外観特
性、衝撃強度のバランスをABS樹脂代替可能な
水準まで改良した耐熱ゴム変性スチレン系樹脂組
成物を提供することを目的とするものでる。
本発明者らは、この課題を達成するために、α
−メチルスチレンを導入したゴム変性スチレン系
樹脂組成物において、ゴム状弾性体よりなる分散
粒子の粒子径分布と添加剤の組合せを詳細に研究
し、粒子径分布を適正に調整し、かつ、ある種の
添加剤を適量加えるならば、上記外観特性、衝撃
強度のバランスが向上した優れた耐熱ゴム変性ス
チレン系樹脂組成物が得られることを見い出し
た。
すなわち、ゴム状弾性体を分散粒子として含有
するゴム変性スチレン系樹脂組成物において、
(A)連続相がスチレンとα−メチルスチレンとよ
り成り、α−メチルスチレン含有量が10〜40重量
%であり(B)分散相の()分散粒子の粒子径が
7500Å未満である分散粒子が25%以上70%未満で
あり、()分散粒子の粒子径が7500Å以上21500
Å未満である分散粒子が25%以上であり、()
分散粒子の粒子径が21500Å以上である分散粒子
が18%以下であり、かつ、分散粒子の粒子径が連
続的な分布を有し、(C)ゴム変性スチレン系樹脂組
成物100重量部に対して有機ポリシロキサンを
0.02重量部以上、0.2重量部以下含有することを
特徴とする外観、衝撃強度、耐熱性に優れたゴム
変性スチレン系樹脂組成物である。
本発明において、連続相中のα−メチルスチレ
ンの含有量が10重量%未満の場合は、耐熱性が低
下する。又、40重量%を超える場合は生産性が低
下し、かつ分子量が高くならず本発明の方法を用
いても衝撃強度が向上しない。
分散粒子の粒子径が7500Å未満の分散粒子が70
%を超える場合は衝撃強度が低下し、25%未満で
は外観特性が低下する。又、粒子径が7500Å以上
21500Å未満の分散粒子が25%未満の場合は衝撃
強度が低下する。粒子径が21500Å以上の分散粒
子が18%を超えると外観特性が低下し、かつ、添
加剤の効果が減少して衝撃強度が低下する。
有機ポリシロキサン0.02重量部未満の場合は衝
撃強度補強効果が得られない。又、有機ポリシロ
キサン0.2重量部を超える場合は、より以上の衝
撃強度補強効果が認められず剛性の低下を招き、
成形時のスエツテイング現象の原因となりかつ、
コストアツプとなるため好ましくない。
なお、本発明で言う分散粒子の粒子径とは、樹
脂の超薄切片法による透過型電子顕微鏡写真拡大
倍率10000を撮影し、写真中の分散粒子約800〜
2000個の粒子数を測定して求めたものである。測
定時、表−1の様に級別し、ある範囲の粒子径を
有する分散粒子の割合は次式より求める。
分散粒子の割合(%)=100NiDi/ΣNiDi
Niは粒子径Diを有する分散粒子の個数である。
The present invention relates to a rubber-modified styrenic resin composition that has excellent appearance, impact strength, and heat resistance. Conventionally, ABS resin has been used as a resin with high heat resistance, high gloss, and high impact strength, and is used in home appliances, audio equipment, automobile parts, etc. recently,
As the cost reduction trend in these applications increases, there is a strong tendency to substitute cheaper rubber-modified styrene resins. When replacing rubber-modified styrenic resin with the physical properties of ABS resin (heat resistance, appearance characteristics,
impact strength). Although the balance between appearance characteristics and impact strength of conventional rubber-modified styrenic resins has been improved by controlling the average particle size of the rubber-like elastomer,
It has not yet reached the point where it fully satisfies market demands.
Furthermore, even if unreacted monomers, oligomers, etc. are removed as much as possible, the heat resistance is limited to a heating deformation temperature of 83 to 84°C, and the market requirement of 87 to 90°C cannot be achieved. The object of the present invention is to provide a heat-resistant rubber-modified styrenic resin composition that incorporates α-methylstyrene and has improved the balance of appearance characteristics and impact strength to a level that can replace ABS resin. In order to accomplish this task, the present inventors have developed α
- In a rubber-modified styrenic resin composition incorporating methylstyrene, the particle size distribution of dispersed particles made of a rubber-like elastic body and the combination of additives were studied in detail, and the particle size distribution was appropriately adjusted and It has been discovered that if an appropriate amount of the seed additive is added, an excellent heat-resistant rubber-modified styrenic resin composition with an improved balance of the above-mentioned appearance characteristics and impact strength can be obtained. That is, in a rubber-modified styrenic resin composition containing a rubbery elastomer as dispersed particles, (A) the continuous phase consists of styrene and α-methylstyrene, and the α-methylstyrene content is 10 to 40% by weight. Yes (B) The particle size of the dispersed particles () of the dispersed phase is
25% or more and less than 70% of the dispersed particles are less than 7500 Å, and () the particle diameter of the dispersed particles is 7500 Å or more 21500
25% or more of the dispersed particles are less than Å ()
18% or less of the dispersed particles have a particle size of 21,500 Å or more, and the particle size of the dispersed particles has a continuous distribution, and (C) based on 100 parts by weight of the rubber-modified styrenic resin composition. organic polysiloxane
This is a rubber-modified styrenic resin composition with excellent appearance, impact strength, and heat resistance, characterized by containing 0.02 parts by weight or more and 0.2 parts by weight or less. In the present invention, if the content of α-methylstyrene in the continuous phase is less than 10% by weight, heat resistance will decrease. If it exceeds 40% by weight, productivity will decrease and the molecular weight will not increase and impact strength will not improve even if the method of the present invention is used. Dispersed particles with a particle diameter of less than 7500 Å are 70
If it exceeds 25%, the impact strength will decrease, and if it is less than 25%, the appearance characteristics will decrease. Also, the particle size is 7500Å or more
If the dispersed particles of less than 21500 Å are less than 25%, the impact strength decreases. If the proportion of dispersed particles with a particle size of 21,500 Å or more exceeds 18%, the appearance characteristics will deteriorate, and the effect of additives will decrease, resulting in a decrease in impact strength. If the amount of organic polysiloxane is less than 0.02 parts by weight, no impact strength reinforcing effect can be obtained. In addition, if the amount of organic polysiloxane exceeds 0.2 parts by weight, no further impact strength reinforcement effect will be observed, leading to a decrease in rigidity.
It causes the sweating phenomenon during molding, and
This is not preferable because it increases costs. In addition, the particle size of the dispersed particles in the present invention refers to the diameter of the dispersed particles in the photo taken with a transmission electron microscope taken at a magnification of 10,000 using an ultra-thin section method of the resin.
This was determined by measuring the number of 2000 particles. At the time of measurement, the particles are classified as shown in Table 1, and the proportion of dispersed particles having a particle size within a certain range is determined by the following formula. Ratio (%) of dispersed particles=100NiDi/ΣNiDi Ni is the number of dispersed particles having particle diameter Di.
【表】【table】
Claims (1)
又はこれとポリスチレンとの混合物であつて、
α−メチルスチレン含有量が10〜40重量%であ
る、重合体又は重合体混合物を連続相とし、 (B)() 粒子径が7500Å未満の粒子が25%以上70
%未満 () 粒子径が7500Å以上21500Å未満での粒
子が25%以上 () 粒子径が21500Å以上の粒子が18%以下
の、連続的な粒子径分布を有するゴム状弾性
体の分散粒子を分散相とする ゴム変性スチレン系樹脂組成物100重量部と 有機ポリシロキサン0.02重量部〜0.2重量部
とを含有する ゴム変性スチレン系樹脂組成物。[Scope of Claims] 1 (A) A styrene-α-methylstyrene copolymer or a mixture of this and polystyrene,
The continuous phase is a polymer or polymer mixture with an α-methylstyrene content of 10 to 40% by weight, and (B)() 25% or more of particles with a particle size of less than 7500 Å70
Less than % () 25% or more of particles with a particle size of 7500 Å or more and less than 21500 Å () 18% or less of particles with a particle size of 21500 Å or more, dispersed particles of rubber-like elastic material with a continuous particle size distribution A rubber-modified styrenic resin composition containing 100 parts by weight of a rubber-modified styrenic resin composition as a phase and 0.02 to 0.2 parts by weight of an organic polysiloxane.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008484A JPS60166338A (en) | 1984-02-08 | 1984-02-08 | Rubber-modified styrenic resin composition having improved appearance, impact strength and heat resistance |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008484A JPS60166338A (en) | 1984-02-08 | 1984-02-08 | Rubber-modified styrenic resin composition having improved appearance, impact strength and heat resistance |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11753791A Division JPH04227649A (en) | 1991-05-22 | 1991-05-22 | Rubber-modified heat-resistant styrenic resin composition excellent in appearance and impact properties |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60166338A JPS60166338A (en) | 1985-08-29 |
| JPH0422178B2 true JPH0422178B2 (en) | 1992-04-15 |
Family
ID=12017235
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008484A Granted JPS60166338A (en) | 1984-02-08 | 1984-02-08 | Rubber-modified styrenic resin composition having improved appearance, impact strength and heat resistance |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60166338A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL193458C (en) * | 1985-10-22 | 1999-11-02 | Asahi Chemical Ind | Process for the continuous preparation of a rubber-reinforced polystyrene composition with a high impact strength. |
| US5185394A (en) * | 1988-05-23 | 1993-02-09 | Mitsui Toatsu Chemicals, Inc. | Rubber-modified styrene type resin composition excellent in sliding properties |
| JPH02145637A (en) * | 1988-11-29 | 1990-06-05 | Asahi Chem Ind Co Ltd | Rubber-modified styrenic resin composition having improved slidability |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1518412A (en) * | 1975-05-15 | 1978-07-19 | Labofina Sa | High-impact polystyrene and process for the production thereof |
| JPS5731946A (en) * | 1980-08-04 | 1982-02-20 | Kanegafuchi Chem Ind Co Ltd | Thermoplastic resin composition |
| JPS57172948A (en) * | 1981-04-17 | 1982-10-25 | Mitsui Toatsu Chem Inc | Rubber-modified styrene resin composition |
| JPS57187346A (en) * | 1981-05-14 | 1982-11-18 | Mitsui Toatsu Chem Inc | Improved rubber-modified styrene resin composition |
-
1984
- 1984-02-08 JP JP2008484A patent/JPS60166338A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60166338A (en) | 1985-08-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH0468326B2 (en) | ||
| TW212808B (en) | ||
| KR101150016B1 (en) | Styrenic themoplastic resin compositions with good mechanical properties and low gloss | |
| JPH0463099B2 (en) | ||
| JPH0422178B2 (en) | ||
| JPH0554500B2 (en) | ||
| JPH0133485B2 (en) | ||
| JPH0525897B2 (en) | ||
| JPS6351460B2 (en) | ||
| JPS5827738A (en) | Thermoplastic formation material | |
| JPS5928342B2 (en) | Impact resistant vinyl chloride resin composition | |
| CA1326575C (en) | Rubber-modified styrene resin composition | |
| JPS62179548A (en) | Impact-resistant polystyrene resin composition | |
| JPH0480061B2 (en) | ||
| JPS6150488B2 (en) | ||
| JPS63221145A (en) | Rubber-modified polystyrene resin composition | |
| JPS6128540A (en) | Polymer composition and manufacture | |
| JPS6326774B2 (en) | ||
| JPS6241538B2 (en) | ||
| JPS6369855A (en) | Resin composition | |
| JPH072821B2 (en) | Matting thermoplastic resin composition and method for producing the same | |
| KR102721861B1 (en) | Method for preparing core-shell copolymer, core-shell copolymer produced by the method and resin composition comprising the copolymer | |
| JP3177621B2 (en) | Damping composition | |
| JPH04220409A (en) | Copolymer resin and thermoplastic resin composition containing the same | |
| JPH01275649A (en) | Rubber-modified polystyrene resin composition excellent in gloss and impact resistance |