JPS58132038A - Wear-resistant styrene resin composition and production thereof - Google Patents

Wear-resistant styrene resin composition and production thereof

Info

Publication number
JPS58132038A
JPS58132038A JP1461282A JP1461282A JPS58132038A JP S58132038 A JPS58132038 A JP S58132038A JP 1461282 A JP1461282 A JP 1461282A JP 1461282 A JP1461282 A JP 1461282A JP S58132038 A JPS58132038 A JP S58132038A
Authority
JP
Japan
Prior art keywords
weight
styrene resin
parts
glass beads
silicone oil
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
JP1461282A
Other languages
Japanese (ja)
Inventor
Takeshi Sakai
猛 坂井
Takashi Suzuki
喬 鈴木
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Kasei Polytec Co
Original Assignee
Mitsubishi Monsanto Chemical Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsubishi Monsanto Chemical Co filed Critical Mitsubishi Monsanto Chemical Co
Priority to JP1461282A priority Critical patent/JPS58132038A/en
Publication of JPS58132038A publication Critical patent/JPS58132038A/en
Pending legal-status Critical Current

Links

Landscapes

  • Processes Of Treating Macromolecular Substances (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain a styrene resin compsn, having excellent wear resistance and a smooth surface by a simple operation, by spreading a silicone oil on the surface of styrene resin pellet, and kneading the pellet and glass beads by using a single screw extruder. CONSTITUTION:1-6pts. wt. silicone oil is mixed with 100pts.wt. styrene resin pellet such as polystyrene or ABS resin by means of a tumbling mixer to spread the silicone oil on the surface of the pellet. 5-35pts.wt. glass beads having a weight-average particle size of 5-50mum are kneaded with said silicone oil- spread styrene resin pellet by using a single screw extruder to obtain the desired wear-resistant styrene resin compsn. Glass beads whose surface is treated with an acrylsilane or an aminosilane, are preferred.

Description

【発明の詳細な説明】 本発明は、耐摩耗性スチレン系樹脂組成物に関する。[Detailed description of the invention] The present invention relates to a wear-resistant styrenic resin composition.

スチレン系樹脂、すなわち、スチレン、α−メチルスチ
レン等の芳香族ビニル単量体を単独で重合させてなるポ
リスチレン等の重合体、ト記芳香族ビニル単量体及びこ
れらの単量体と共重合可能な単量体、例えばアクリロニ
トリル、メタクリロニトリル等と共重合させて得られる
AS樹脂等の共重合体、ポリブタジェン等のゴム状弾性
体に芳香族ビニル単量体及びこれと共重合可能な単量体
をグラフト共重合してなるABS樹脂等の共重合体等は
、良好な成形加工性、耐衝撃性1.耐薬品性を有するの
で広く使用されている。
Styrenic resins, i.e., polymers such as polystyrene obtained by polymerizing aromatic vinyl monomers such as styrene and α-methylstyrene alone, aromatic vinyl monomers listed above, and copolymers with these monomers. Copolymers such as AS resin obtained by copolymerizing with possible monomers such as acrylonitrile, methacrylonitrile, etc., aromatic vinyl monomers and monomers copolymerizable with these, rubber-like elastic bodies such as polybutadiene, etc. Copolymers such as ABS resins made by graft copolymerizing polymers have good moldability and impact resistance. It is widely used because it has chemical resistance.

これらの樹脂は、耐摩耗性が不十分であるため、従来、
ガラスピーズ等の無機充填剤を配合する等の対策を講じ
ていた。
Conventionally, these resins have insufficient wear resistance, so
Measures were taken such as adding inorganic fillers such as glass peas.

特に、ガラスピーズは球状であるのでスチレン系樹脂等
に配合しても成形、品の物性に異方性が生じないこと、
繊維状の充填材に比較して表面が清めらかであること等
の特徴を有しているが、スチレン系樹脂等と混練する場
合、樹脂がベレット状であると単軸押出機等の一般的な
装置では均一に分散できないので、バンパ’J −ミキ
サー、加圧式ニーダ−等の大規模な装置を用いるか、粉
末樹脂を使用する必要があった。
In particular, since glass beads are spherical, even when blended with styrene resin, etc., there will be no anisotropy in the physical properties of the product and molding.
It has characteristics such as a smooth surface compared to fibrous fillers, but when kneading with styrene resin, etc., the resin is in the form of a pellet, making it difficult to use a general single-screw extruder, etc. Since uniform dispersion cannot be achieved using conventional equipment, it has been necessary to use large-scale equipment such as a Bumper'J-mixer or a pressure kneader, or to use powdered resin.

本発明者等は、上記の従来技術の問題点を解決し、より
耐摩耗性が優れかつ表面の滑らかなスチレン系樹脂組成
物及びそのより簡便な製造方法を開発することを目的と
して鋭意研究を重ねた結果本発明に到達したものである
The present inventors have conducted extensive research with the aim of solving the problems of the prior art described above and developing a styrenic resin composition with better wear resistance and a smoother surface, and a simpler manufacturing method. As a result of repeated efforts, the present invention was arrived at.

本発明の第7の目的は、耐摩耗性が優れ、かつ表面の滑
らかなスチレン系樹脂組成物を提供することにあり、こ
の目的は本発明に従いスチレン系樹脂100重量部に対
してガラスピーズ5〜35重量部及びシリコンオイルl
°〜6重量部を配合してなる耐摩耗性スチレン系樹脂組
成物によって達せられる。
A seventh object of the present invention is to provide a styrenic resin composition with excellent abrasion resistance and a smooth surface. ~35 parts by weight and l silicone oil
This is achieved by a wear-resistant styrenic resin composition containing 6 parts by weight.

また、本発明の第コの目的は、耐摩耗性に優れ、かつ表
面の滑らかなスチレン系樹脂組成物を簡便な操作で製造
し得る方法を提供することにあり、この目的は本発明に
従いスチレン系樹脂にガラスピーズを配合して耐摩耗性
スチレン系樹脂組成物を製造する方法において、スチレ
ン系樹脂ペレット10O重量部に、予じめソリコンオイ
ル7〜6重量部を展着したものとガラスピーズ5〜35
重量部を単軸押出機により混練することにより達せられ
る。
A third object of the present invention is to provide a method for producing a styrene resin composition with excellent abrasion resistance and a smooth surface by a simple operation. In a method of manufacturing a wear-resistant styrenic resin composition by blending glass beads into a resin, 100 parts by weight of styrene resin pellets are mixed with 7 to 6 parts by weight of soric oil and 5 parts by weight of glass beads. ~35
This can be achieved by kneading parts by weight using a single screw extruder.

本発明に用いられるガラスピーズは重量平均粒径が5−
soμm、好ましくは、5〜20μmのものが適当であ
り、表面がアクリルシラン、グリシドシラン、アミノシ
ラン等で処理されているものがより好ましい。
The glass beads used in the present invention have a weight average particle size of 5-
Soum, preferably 5 to 20 um, is suitable, and those whose surface has been treated with acrylic silane, glycido silane, amino silane, etc. are more preferred.

ガラスピーズの配合比率は、ポリスチレン、AS樹脂、
ABS樹脂等のスチレン系樹脂100重量部当り5〜3
5重量部、より好ましくは、10〜30重量部が適当で
ある。
The blending ratio of glass beads is polystyrene, AS resin,
5 to 3 per 100 parts by weight of styrene resin such as ABS resin
A suitable amount is 5 parts by weight, more preferably 10 to 30 parts by weight.

スチレン系樹脂の形状はベレット、すなわち、粒径敢闘
程度の粒状のものでも、粉末であっても特に問題はない
が、ペレット状のものがより取り扱いが容易である。
The shape of the styrenic resin may be pellets, that is, particles with a size comparable to those of average size, or powder, but there is no particular problem, but pellets are easier to handle.

ガラスピーズの配合比率は、5重量部未満では、耐摩耗
性があまり向上せず、また、35重量部を越えるときは
、ガラスピーズのスチレン系樹脂中での分散が不良とな
り好ましくない。
If the blending ratio of glass beads is less than 5 parts by weight, the abrasion resistance will not improve much, and if it exceeds 35 parts by weight, the dispersion of the glass beads in the styrene resin will be poor, which is not preferable.

シリコンオイルは、通常のポリアルキルシロキサン、ポ
リアリールシロキサン類でよく、添加量は、スチレン系
樹脂10θ重量部当り/ −A重量部、好ましくは、l
、5〜3重量部が適当である。
The silicone oil may be a conventional polyalkylsiloxane or polyarylsiloxane, and the amount added is preferably 1/-A parts by weight per 10θ parts by weight of the styrene resin.
, 5 to 3 parts by weight is suitable.

1重量部未満では、シリコンオイルを添加した効果はあ
られれず、6重量部を越えるときはスチレン系樹脂成形
品の表面において剥離が起り、また成形収縮率が大きく
なるので好壕しくない。
If the amount is less than 1 part by weight, the effect of adding silicone oil will not be obtained, and if it exceeds 6 parts by weight, peeling will occur on the surface of the styrene resin molded product and the molding shrinkage rate will increase, which is not desirable.

本発明に係るガラスピーズ及びシリコンオイルを配合し
た組成物は単にスチレン系樹脂にガラスピーズを配合し
たものと比較して、摩擦係数が低下し、また、耐摩耗性
が向上する。すなわち、後述する摩耗輪による摩耗減量
が著るしく減少し、シリコンオイルの添加に伴なう相乗
効果は著るしいものがある。
A composition in which glass beads and silicone oil according to the present invention are blended has a lower coefficient of friction and improved wear resistance than a composition in which glass beads are simply blended with a styrene resin. That is, the wear loss due to the worn wheels, which will be described later, is significantly reduced, and the synergistic effect accompanying the addition of silicone oil is significant.

本発明に係る組成物は、スチレン系樹脂、ガラスピーズ
及びシリコンオーイルの各所定量をバンバリーミキサ−
、ロール、加圧式ニーダ−等によって混練する方法また
は粉末状の樹脂を用いて単軸押出機により混練する方法
によってももちろん製造できるが、取り扱い容易なペン
ツ粉末状樹脂を用いることなく単軸押出機によりガラス
ピーズを均一に混線、分散させることができる。この場
合、ガラスピーズは単軸押出機のホッパーに上記ペレッ
トと共に投入するのが望ましい。この方法によると大が
かりな装・置を使用する必要がな〈産業上の利用価値は
極めて大である。  。
The composition according to the present invention is prepared by adding predetermined amounts of styrene resin, glass beads, and silicone oil to a Banbury mixer.
Of course, it can also be produced by kneading with rolls, pressure kneaders, etc., or by kneading with a single-screw extruder using powdered resin, but it can also be produced using a single-screw extruder without using the easy-to-handle Pentz powdered resin. This makes it possible to cross-wire and disperse the glass beads uniformly. In this case, it is desirable that the glass peas be placed in the hopper of a single-screw extruder together with the pellets. According to this method, there is no need to use large-scale equipment and equipment (the industrial value is extremely large). .

続いて1、実施例及び比較例に基づいて本発明をさらに
具体的に説明する。
Next, the present invention will be explained in more detail based on 1. Examples and Comparative Examples.

なお、実施例及び比較例において、耐摩耗性はJ工5K
−710’l に規定される摩耗輪によるプラスチック
の摩耗試験方法にしたがって摩耗減量を測定した。この
場合、摩耗輪に、研摩材H−lざを用いたもの及び炭素
鋼(j9!ro)を用いたもののコ種の場合について測
定した。
In addition, in the examples and comparative examples, the wear resistance is J-5K.
The abrasion loss was measured according to the plastic abrasion test method using an abrasion wheel specified in -710'l. In this case, measurements were made for two types of wear wheels: one using abrasive material H-1 and one using carbon steel (J9!RO).

また、摩擦係数は、3fの傾斜面に試料を取り付け、重
量/ 7 ’1.2 、r、接触面積//calの炭素
鋼(sysa)製の重錘を用いて測定した。
Further, the friction coefficient was measured by attaching the sample to a 3F inclined surface and using a weight made of carbon steel (SYSA) with weight/7'1.2, r and contact area//cal.

実施例/ ABEI樹脂(三菱モンサント化成■製タフレックス−
2IO、タフレックスは同社登録商標)ペレテト100
重量部にシリコンオイル(トーレーシリコン■製、SH
−コoo粘度lコ、so。
Example / ABEI resin (Tufflex manufactured by Mitsubishi Monsanto Chemical)
2IO, TAFLEX are registered trademarks of the company) PELLETET 100
Silicone oil (manufactured by Toray Silicone, SH) in the weight part
-kooo viscosity lko, so.

ap)コ、45重量部を添加、タンブラ−ミキサーで混
合した。
45 parts by weight of ap) were added and mixed in a tumbler mixer.

得られたシリコンオイルを展着したABS樹脂ペレット
とガラスピーズ(東芝バロテイーニ■製、FiGB7.
?10.アルカリガラスピーズ、アクリルシラン処理)
/ 7.4重量部を、スクリュー径4’ 0 *ms 
L/D (スクリュー外径−軸長比)ココの単軸押出機
によりシリンダ一温度230℃で混練した。得られたペ
レットを射出成形して試料を作製して物性を測定した。
ABS resin pellets and glass beads (manufactured by Toshiba Balloteini ■, FiGB7.
? 10. Alkali glass beads, acrylic silane treatment)
/ 7.4 parts by weight, screw diameter 4' 0 *ms
L/D (screw outer diameter-shaft length ratio) Kneaded at a cylinder temperature of 230°C using a single-screw extruder. The obtained pellets were injection molded to prepare samples and their physical properties were measured.

静摩擦係数0.15、動摩擦係数0./ 3、摩耗減量
は、摩耗輪H−1g、荷重/θoog、試験回数100
0回の条件(以下「H−ig摩耗減量」という。)で測
定して、2 !; Om9、摩耗輪S IIS C,荷
重/300g、試験回数qoo。
Static friction coefficient 0.15, dynamic friction coefficient 0. / 3. Wear loss is wear wheel H-1g, load/θoog, number of tests 100
Measured under the condition of 0 times (hereinafter referred to as "H-ig wear loss"), 2! ; Om9, wear wheel S IIS C, load/300g, number of tests qoo.

回の条件(以下「541SC摩耗減量」という。)で測
定してo m9であった。
It was measured under the conditions of 541SC (hereinafter referred to as "541SC abrasion loss") and found to be 0 m9.

実施例コ 実施例1で用いたものと同様のABS樹脂ベレット10
θ重量部に対して、シリコンオイル7.6重量部及びガ
ラスピーズ11重量部を実施例1と同様の方法で混練し
てガラスピーズ含有ABS樹脂組成物を製造した。
Example ABS resin pellet 10 similar to that used in Example 1
7.6 parts by weight of silicone oil and 11 parts by weight of glass beads were kneaded with respect to θ parts by weight in the same manner as in Example 1 to produce an ABS resin composition containing glass beads.

この組成物を用いて作製した試料の静摩擦係数は0./
&、動摩擦係数は0./3、H−/II摩耗減量は21
.Q■、E19jO摩耗減量はO〜であった。
The static friction coefficient of the sample prepared using this composition was 0. /
&, the coefficient of dynamic friction is 0. /3, H-/II wear loss is 21
.. Q■, E19jO abrasion loss was O~.

実施例3 ABS樹脂ペレット100重量部に対して、シリコンオ
イル3.75重量部、及びガラスピーズ25重量部を実
施例1と同様の方法で混練してガラスピーズ含有ABS
樹脂組成物を製造した。なお、ABEI樹脂、シリコン
オイル及びガラスピーズは実施例1で用いたものと同一
の品種である。
Example 3 100 parts by weight of ABS resin pellets, 3.75 parts by weight of silicone oil, and 25 parts by weight of glass peas were kneaded in the same manner as in Example 1 to produce ABS containing glass peas.
A resin composition was produced. Note that the ABEI resin, silicone oil, and glass beads are the same types as those used in Example 1.

静摩擦係数0./グ、動摩擦係数O1/3、H−/ g
摩耗減量230〜、BQ!10摩耗減量はθ■であった
Static friction coefficient 0. /g, dynamic friction coefficient O1/3, H-/g
Wear loss: 230~, BQ! 10 The wear loss was θ■.

比較例1 実施例1で用いたABS樹脂の物性を測定したところ、
静摩擦係数0.1g、動摩擦係数o、iq、H−1g摩
耗減量boom9.5tisa摩耗減量λj〜であった
Comparative Example 1 When the physical properties of the ABS resin used in Example 1 were measured,
The static friction coefficient was 0.1g, the dynamic friction coefficient o, iq, H-1g abrasion loss boom 9.5tisa abrasion loss λj~.

比較例コ シリコンオイルを添加しなかったこと以外は実施例−と
同様にしてガラスピーズ含有ABS樹脂組成物を製造し
た。
Comparative Example An ABS resin composition containing glass beads was produced in the same manner as in Example except that silicone oil was not added.

得られた組成物の静摩擦係数は0.1g、動摩擦係数は
(7/?、H−/g摩耗減量ダー〇〜、5ttsc摩耗
減量15m9であった。
The resulting composition had a static friction coefficient of 0.1 g, a dynamic friction coefficient of (7/?, H-/g abrasion loss 0~, 5ttsc abrasion loss 15 m9).

比較例3 シリコンオイルを添加しなかったこと以外は実施例3と
同様にしてガラスピーズ含有ABS樹脂組成物を製造し
た。
Comparative Example 3 An ABS resin composition containing glass beads was produced in the same manner as in Example 3 except that silicone oil was not added.

得られたものの静摩擦係数はo、iざ、動摩擦係数はθ
、/り、H−/g摩耗減量は390m9.5tisc摩
耗減量は1gmgであった。
The static friction coefficient of the obtained product is o, iza, and the kinetic friction coefficient is θ.
,/ri, H-/g abrasion loss was 390m9.5tisc abrasion loss was 1gmg.

実施例ダ As樹脂(三菱モンサンド化成■ サンレックス−H1
サンレックスは同社登録商標)ペレット10O重量部に
実施例1と同様のシリコンオイルハロ7重量部を添加し
タンブラ−ミキサーで混合した。得られた混合物とガラ
スピーズ(実施例/と同様)l1重量部を実施例1゛で
用いた単軸押出機を用いてコ3θ℃で混練した。
Example: As resin (Mitsubishi Monsando Kasei Sunrex-H1
7 parts by weight of the same silicone oil halo as in Example 1 was added to 10 parts by weight of Sunrex (registered trademark) pellets and mixed in a tumbler mixer. The obtained mixture and 1 part by weight of glass peas (same as in Example) were kneaded at 3θ°C using the single screw extruder used in Example 1.

得られた組成物を用いて射出成形した試料の静摩擦係数
は0./II、動摩擦係数は0.13、またH−1g摩
耗減量はりorn9、sysa摩粍減量はQ〜であった
The static friction coefficient of a sample injection molded using the obtained composition was 0. /II, the dynamic friction coefficient was 0.13, the H-1g abrasion loss was or9, and the sysa abrasion loss was Q~.

なお、本実施例で用いたAs樹脂の静摩擦係数はo、i
 g、動摩擦係数は0.2g、H−1g摩耗減量は/ 
50 m9、またSグ、5−0摩耗減量はコOνであっ
た。
Note that the static friction coefficients of the As resin used in this example are o, i
g, dynamic friction coefficient is 0.2g, H-1g wear loss is /
50 m9, Sg, 5-0 wear loss was Ov.

比較例ダ シ1ナコンオイルを加えなかった点以外は実施例qと同
様にしてガラスピーズ含有As樹脂組成物ペレットを製
造した。
Comparative Example Dashi 1 Glass beads-containing As resin composition pellets were produced in the same manner as in Example q except that no Nacon oil was added.

この組成物の静、摩擦係数は0./ 7、動摩擦係数は
0.2g%H−/g摩耗減量/10m9、またSすSC
摩耗減量は/!;m9であった。
The static friction coefficient of this composition is 0. / 7, Dynamic friction coefficient is 0.2g%H-/g wear loss/10m9, and SSC
Wear loss is /! ; It was m9.

Claims (2)

【特許請求の範囲】[Claims] (1)スチレン系樹脂709重量部に対してガラスビー
ズ5〜35重量部及びシリコンオイル7〜6重量部を配
合してなる耐摩耗性スチレン系樹脂組成物。
(1) A wear-resistant styrenic resin composition comprising 709 parts by weight of styrene resin and 5 to 35 parts by weight of glass beads and 7 to 6 parts by weight of silicone oil.
(2)  スチレン系樹脂にガラスピーズを配合して耐
摩耗性スチレン系樹脂組成物を製造する方法において、
スチレン系樹脂ペレット10θ重量部に勇じめシリコン
オイル7〜6重量部を展着したものとガラスピーズ5〜
3!f重量部を単軸押出機により混練することを特徴と
する方法。
(2) In a method for producing a wear-resistant styrenic resin composition by blending glass beads with a styrenic resin,
Styrene resin pellets with 10θ parts by weight spread with 7 to 6 parts by weight of courageous silicone oil and 5 to 5 parts by weight of glass beads.
3! A method characterized in that part by weight of f is kneaded using a single screw extruder.
JP1461282A 1982-02-01 1982-02-01 Wear-resistant styrene resin composition and production thereof Pending JPS58132038A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1461282A JPS58132038A (en) 1982-02-01 1982-02-01 Wear-resistant styrene resin composition and production thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1461282A JPS58132038A (en) 1982-02-01 1982-02-01 Wear-resistant styrene resin composition and production thereof

Publications (1)

Publication Number Publication Date
JPS58132038A true JPS58132038A (en) 1983-08-06

Family

ID=11866020

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1461282A Pending JPS58132038A (en) 1982-02-01 1982-02-01 Wear-resistant styrene resin composition and production thereof

Country Status (1)

Country Link
JP (1) JPS58132038A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01280508A (en) * 1988-03-04 1989-11-10 W R Grace & Co Melt extruded polymer composition and molding method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01280508A (en) * 1988-03-04 1989-11-10 W R Grace & Co Melt extruded polymer composition and molding method thereof

Similar Documents

Publication Publication Date Title
JPH0229695B2 (en)
JP2006522175A (en) Composite powder, its manufacture and use
JPS60147451A (en) Improved rubber blend containing zinc dimethacrylate
JPS61185557A (en) Antistatic thermoplastic composition
US4427831A (en) Rubber materials having excellent grip on ice
CN108299690A (en) Polyurethane shoe-sole and preparation method thereof
JPS58132038A (en) Wear-resistant styrene resin composition and production thereof
EP3686244A1 (en) Heat-resistant resin composition
JPH01217053A (en) Humidity crosslinkable elastic plastic composition and crosslinked soft article
JPS6346242A (en) Rubber composition
US3654218A (en) Process of forming an elastomer-carbon black mixture
EP0104247A4 (en) Process for preparation of free flowing particles.
JPH05132605A (en) Rubber-modified polystyrene composition
JP2018188587A (en) Rubber composition for tire
JPS5928342B2 (en) Impact resistant vinyl chloride resin composition
JP3289360B2 (en) Silica composite granules
JPH01236270A (en) Resin composition
JPH01306443A (en) Vulcanizable rubber composition
JPS5773033A (en) Talc-containing propylene polymer composition
Kurian et al. Scanning electron microscopy studies on wear of HDPE-filled natural rubber vulcanizates
JPS6046135B2 (en) Sponge-like elastic body
CN114479133A (en) Application and preparation method of powder styrene butadiene rubber friction material
JPH0794593B2 (en) Thermoplastic resin composition
JP2006241348A (en) Rubber composition for tire
JPH0676464B2 (en) Method for producing styrene resin