JPH05311074A - Aromatic polysulfone molding composition - Google Patents

Aromatic polysulfone molding composition

Info

Publication number
JPH05311074A
JPH05311074A JP12192992A JP12192992A JPH05311074A JP H05311074 A JPH05311074 A JP H05311074A JP 12192992 A JP12192992 A JP 12192992A JP 12192992 A JP12192992 A JP 12192992A JP H05311074 A JPH05311074 A JP H05311074A
Authority
JP
Japan
Prior art keywords
aromatic polysulfone
weight
etfe
parts
mold
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.)
Granted
Application number
JP12192992A
Other languages
Japanese (ja)
Other versions
JP3152255B2 (en
Inventor
Yoshihisa Yamamoto
喜久 山本
Tetsuo Shimizu
哲男 清水
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.)
Daikin Industries Ltd
Original Assignee
Daikin Industries Ltd
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 Daikin Industries Ltd filed Critical Daikin Industries Ltd
Priority to JP12192992A priority Critical patent/JP3152255B2/en
Publication of JPH05311074A publication Critical patent/JPH05311074A/en
Application granted granted Critical
Publication of JP3152255B2 publication Critical patent/JP3152255B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To obtain an aromatic polysulfone molding composition of improved moldability. CONSTITUTION:100 pts.wt. aromatic polysulfone is mixed with 0.3-5 pts.wt. ethylene/tetrafluoroethylene copolymer and 0-25 pts.wt. carbon fiber or powder to obtain the composition markedly improved in moldability, especially molding flow, inhibition of mold deposit and mold release.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は芳香族ポリスルホンに特
定のフルオロカーボン重合体を微量含有せしめることに
より、芳香族ポリスルホンの成形性を改善することがで
きる成形用組成物に関する。さらに詳しくは、本発明に
よれば、射出成形時の流動性、モールドデポジット、離
型性を改良することができる。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a molding composition which can improve the moldability of an aromatic polysulfone by containing a small amount of a specific fluorocarbon polymer in the aromatic polysulfone. More specifically, according to the present invention, it is possible to improve fluidity, mold deposit and mold releasability during injection molding.

【0002】[0002]

【従来の技術】芳香族ポリスルホンは非結晶性であるた
め、等方性で成形収縮率が小さく、またガラス転移点が
高いため、高温時の強度、弾性率、耐クリープ性に優れ
る。これらの性質を活かし、高寸法精度、高耐熱性が要
求されるICトレイのような電子部材やOA、AV機器
部品として広く使用されている。しかし、精密な部品を
射出成形するようなばあい、芳香族ポリスルホンそのも
のの流動性や、成形品を金型から取り出すときの離型
性、数多く成形したときの金型汚れ(いわゆるモールド
デポジット)などという成形性がしばしば問題になり、
成形品の歩留りや生産性に大きな影響を与えている。
2. Description of the Related Art Since aromatic polysulfones are non-crystalline, they are isotropic and have a low molding shrinkage, and since they have a high glass transition point, they are excellent in strength, elastic modulus and creep resistance at high temperatures. Utilizing these properties, they are widely used as electronic members such as IC trays, OA, and AV equipment parts that require high dimensional accuracy and high heat resistance. However, in the case of injection molding of precision parts, the fluidity of the aromatic polysulfone itself, the releasability when the molded products are taken out of the mold, the mold stains when molding many (so-called mold deposit), etc. Moldability often becomes a problem,
It has a great impact on the yield and productivity of molded products.

【0003】これに対し、芳香族ポリスルホンにフッ素
系重合体を混合すれば、自己潤滑特性が付与でき、金型
からの離型性、摺動特性が改良されることが知られてい
る。たとえば特開昭58−160353号公報には、芳
香族ポリスルホン、フッ素系重合体およびオキシベンゾ
イルポリエステルからなる組成物が、軟質金属を相手材
としたときに摩耗特性に優れた摺動材であることが記載
されている。また、ガラス繊維、ウォラストナイトなど
の繊維状強化材やタルク、ガラスビーズなどの無機充填
材を配合して成形収縮率を低減した芳香族ポリスルホン
組成物にフッ素系重合体を配合することで、金型からの
離型性を改良した例が特開昭60−23448号公報に
記載されている。さらに、芳香族ポリスルホン、フッ素
系重合体および炭素繊維とからなる組成物が、優れた摺
動特性を有することが特開昭60−38465号公報に
記載され、特開平3−252457号公報では分子末端
を安定化した特定のフッ素系重合体を配合することによ
り摺動特性、離型性が改良されることが示されている。
On the other hand, it is known that when a fluoropolymer is mixed with an aromatic polysulfone, a self-lubricating property can be imparted, and mold releasability from a mold and sliding property are improved. For example, in JP-A-58-160353, a composition comprising an aromatic polysulfone, a fluoropolymer and oxybenzoyl polyester is a sliding material having excellent wear characteristics when a soft metal is used as a counter material. Is listed. Further, by blending a fluorine-based polymer in an aromatic polysulfone composition having glass fiber, a fibrous reinforcing material such as wollastonite or the like, talc, and an inorganic filler such as glass beads to reduce molding shrinkage, An example in which the releasability from the mold is improved is described in JP-A-60-23448. Further, it is described in JP-A-60-38465 that a composition comprising an aromatic polysulfone, a fluoropolymer and a carbon fiber has excellent sliding properties. In JP-A-3-252457, a molecule is disclosed. It has been shown that the sliding property and the releasability are improved by blending a specific fluoropolymer having a stabilized terminal.

【0004】[0004]

【発明が解決しようとする課題】これらの先行文献中に
記載された実施例のすべてにおいて、組成物中のフッ素
系重合体としてポリテトラフルオロエチレン(PTF
E)が使用されている。確かにPTFEの効果は摺動特
性の改良に有効であり同時に離型性も改善されるが、特
に摺動を目的とせず離型性改良の目的に限れば、PTF
Eのばあい所望の効果をうるためには量が多く必要とな
り、強度など他の物性へ悪影響を与えるなど必ずしも満
足できるものではない。
In all of the examples described in these prior documents, polytetrafluoroethylene (PTF) was used as the fluoropolymer in the composition.
E) is used. Certainly, the effect of PTFE is effective in improving the sliding characteristics, and at the same time, the releasability is also improved.
In the case of E, a large amount is required to obtain the desired effect, which is not always satisfactory because it adversely affects other physical properties such as strength.

【0005】これに対し本発明者らは、通常使用される
PTFEよりもエチレン−テトラフルオロエチレン共重
合体(ETFE)が優れた離型効果を有し、これがPT
FEを配合するよりも有利であることを見出し本発明を
完成するに至った。
On the other hand, the present inventors have found that ethylene-tetrafluoroethylene copolymer (ETFE) has a better releasing effect than PTFE which is usually used, and this is because PT
They have found that it is more advantageous than compounding FE, and completed the present invention.

【0006】[0006]

【課題を解決するための手段】すなわち本発明は、芳香
族ポリスルホン100 重量部に対しETFE0.3 〜5重量
部とカーボン系繊維0〜25重量部が配合されてなる芳香
族ポリスルホン成形用組成物に関する。
That is, the present invention provides an aromatic polysulfone molding composition in which 0.3 to 5 parts by weight of ETFE and 0 to 25 parts by weight of carbon fiber are blended with 100 parts by weight of aromatic polysulfone. Regarding

【0007】前記特開昭60−23448号公報には、
PTFE以外のフッ素系重合体として、たとえばテトラ
フルオロエチレン−パーフロロアルキルビニルエーテル
共重合体(PFA)、エチレン−ヘキサフルオロプロピ
レン共重合体(FEP)、エチレン−テトラフルオロエ
チレン共重合体(ETFE)、ポリクロロトリフルオロ
エチレン(PCTFE)、フッ化ビニリデン樹脂(PV
dF)が明細書中で一般的に記載されているが、その具
体的効果は明らかにされていない。特に、当業者にはE
TFE、PCTFE、PVdFが自己潤滑特性に優れた
樹脂とは通常見なされていない。
The above-mentioned Japanese Patent Laid-Open No. 60-23448 discloses that
As the fluorine-based polymer other than PTFE, for example, tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer (PFA), ethylene-hexafluoropropylene copolymer (FEP), ethylene-tetrafluoroethylene copolymer (ETFE), poly Chlorotrifluoroethylene (PCTFE), vinylidene fluoride resin (PV
dF) is generally mentioned in the description, but its specific effect has not been clarified. Especially for those skilled in the art
TFE, PCTFE and PVdF are not usually regarded as resins having excellent self-lubricating properties.

【0008】しかし、本発明者らはETFEを添加する
とPTFEよりも少量で離型性が改良され、しかも流動
性や、モールドデポジットなども改善されることを見出
したのである。
However, the present inventors have found that the addition of ETFE improves the releasability with a smaller amount than that of PTFE, and also improves the fluidity and mold deposit.

【0009】本発明で用いる芳香族ポリスルホンは、ア
リレン単位がエーテルおよびスルホン結合でつながった
線状高分子であり、UDEL(アモコ社製)、VICT
REX(ICI社製)などの商標で市販されている樹脂
である。また、ETFEはテトラフルオロエチレン−エ
チレンを基本単位とし、通常さらに含フッ素オレフィン
を2〜15重量%導入した共重合体であり、ネオフロンE
TFE(ダイキン工業(株)製)、アフロンCOP(旭
硝子(株)製)、テフゼル(デュポン社製)などの商標
で市販されているものが使用できる。これらのETFE
は297 ℃、5kgの加重で測定される10分間当りに押し出
される樹脂量(MIという)で通常1〜20の溶融流動性
を有する。
The aromatic polysulfone used in the present invention is a linear polymer in which allylene units are connected by ether and sulfone bonds, and is UDEL (manufactured by Amoco), VICT.
It is a resin marketed under the trademark such as REX (manufactured by ICI). Further, ETFE is a copolymer having tetrafluoroethylene-ethylene as a basic unit and usually containing 2 to 15% by weight of a fluorine-containing olefin.
Commercially available products such as TFE (manufactured by Daikin Industries, Ltd.), Aflon COP (manufactured by Asahi Glass Co., Ltd.), and Tefzel (manufactured by DuPont) can be used. These ETFE
Has a melt flowability of usually 1 to 20 in terms of the amount of resin extruded per 10 minutes (referred to as MI) measured at 297 ° C. and a load of 5 kg.

【0010】本発明において配合するETFEの量は、
芳香族ポリスルホン100 重量部に対して0.3 〜5重量部
であり、好ましくは0.5 〜3重量部である。ETFEの
量が0.3 重量部未満のばあいは離型の効果が認め難く、
5重量部を超えるばあいは、成形品の表面にETFEの
分離層が生じ外観がわるくなる。
The amount of ETFE blended in the present invention is
The amount is 0.3 to 5 parts by weight, preferably 0.5 to 3 parts by weight, based on 100 parts by weight of the aromatic polysulfone. If the amount of ETFE is less than 0.3 parts by weight, the effect of mold release is difficult to recognize,
If the amount exceeds 5 parts by weight, a separation layer of ETFE is formed on the surface of the molded product, resulting in a poor appearance.

【0011】本発明においてETFEの配合方法は特に
限定されないが、あらかじめ芳香族ポリスルホンに10重
量%程度までETFEを溶融混合したのち、これを所望
の割合まで芳香族ポリスルホンで溶融希釈することが好
ましい。
In the present invention, the method of blending ETFE is not particularly limited, but it is preferable to melt-mix ETFE up to about 10% by weight with aromatic polysulfone and then melt-dilute this with aromatic polysulfone to a desired ratio.

【0012】本発明におけるETFEによる離型効果
は、強度強化や導電性付与、摺動性付与の目的でカーボ
ン系の繊維または粉末をブレンドするばあい、より効果
的である。カーボン系の繊維または粉末としては、従来
より知られているものが特に限定なく使用されうるが、
たとえばPAN系、ピッチ系、レーヨン系、リグニン系
などの高モジュラスおよび低モジュラスの炭素繊維、ま
たケッチェンブラック、アセチレンブラック、ファーネ
スブラック、ランプブラック、サーマルブラック、チャ
ンネルブラック、ロールブラック、ディスクブラックな
どのカーボンブラック粉末、また黒鉛として土状、鱗
状、鱗片状、塊状などの天然黒鉛および人造黒鉛(石炭
コークス系、石油コークス系、ピッチ系)、さらに球状
あるいはウィスカ状のカーボン粉末などがあげられる。
The releasing effect of ETFE in the present invention is more effective when a carbon fiber or powder is blended for the purpose of strengthening strength, imparting conductivity, and imparting slidability. As the carbon-based fiber or powder, those conventionally known may be used without particular limitation,
For example, high modulus and low modulus carbon fibers such as PAN type, pitch type, rayon type, lignin type, Ketjen black, acetylene black, furnace black, lamp black, thermal black, channel black, roll black, disk black, etc. Carbon black powder, and as graphite, natural graphite and artificial graphite (coal coke-based, petroleum coke-based, pitch-based) such as earth-like, scale-like, scale-like, and lump-like, and spherical or whisker-like carbon powder can be mentioned.

【0013】カーボン系の繊維または粉末は、芳香族ポ
リスルホン100 重量部に対して25重量部以下であること
が好ましい。25重量部を超えると、成形性が低下する。
The amount of carbon fiber or powder is preferably 25 parts by weight or less with respect to 100 parts by weight of aromatic polysulfone. If it exceeds 25 parts by weight, the moldability will decrease.

【0014】また、必要に応じてガラス繊維、セラミッ
ク繊維、チタン酸カリウム繊維、アラミド繊維などの繊
維状の強化材、炭酸カルシウム、タルク、マイカ、クレ
イ、ガラスビーズなどの無機充填材、液晶ポリマー、ポ
リイミドなどの耐熱性樹脂、着色剤などを添加してもよ
い。
If necessary, fibrous reinforcing materials such as glass fibers, ceramic fibers, potassium titanate fibers and aramid fibers, inorganic fillers such as calcium carbonate, talc, mica, clay and glass beads, liquid crystal polymers, A heat resistant resin such as polyimide or a colorant may be added.

【0015】[0015]

【実施例】つぎに本発明の成形用組成物を実施例に基づ
いて説明するが、本発明はかかる実施例のみに限られる
ものではない。
EXAMPLES Next, the molding composition of the present invention will be explained based on examples, but the present invention is not limited to these examples.

【0016】実施例1〜4 芳香族ポリスルホン(アモコ社製UDEL P−170
0)7200gとETFE樹脂(ダイキン工業(株)製ネオ
フロンETFE EP−521)800 gを、2軸混練押
出機((株)東洋精機製作所製ラボプラストミル)を用
いてシリンダー温度310 ℃で混練し、ETFE含量10重
量%の芳香族ポリスルホン組成物をえた。このマスター
バッチを用い、同じ2軸混練押出機で表1に示す配合に
なるように同じ芳香族ポリスルホンで希釈し、さらに実
施例1、3および4については同時にピッチ系カーボン
繊維(呉羽化学工業(株)製M−104T)を混合しペ
レット化した。
Examples 1 to 4 Aromatic polysulfone (UDEL P-170 manufactured by Amoco)
0) 7200 g and ETFE resin (Neotron ETFE EP-521 manufactured by Daikin Industries Ltd.) 800 g were kneaded at a cylinder temperature of 310 ° C. using a twin-screw kneading extruder (Labo Plastomill manufactured by Toyo Seiki Seisakusho KK). , An aromatic polysulfone composition having an ETFE content of 10% by weight was obtained. Using this masterbatch, the mixture was diluted with the same aromatic polysulfone in the same twin-screw kneading extruder to have the composition shown in Table 1, and for Examples 1, 3 and 4, pitch-based carbon fibers (Kureha Chemical Industry (Kureha Chemical Industry M-104T) manufactured by K.K. was mixed and pelletized.

【0017】これらのペレットを射出成形機(日本製鋼
(株)製N−65)を用いて、シリンダー温度330 〜34
0 ℃、金型温度130 ℃でICトレイを成形し、各組成物
の離型効果を調べた。離型効果は、モールドデポジット
などのために離型効果がなくなり、取出し時に成形品が
割れてしまうまでの射出成形ショット回数(限界回数)
によって評価した。また、成形品の外観を目視で観察し
た。結果を表1に示す。
Cylinder temperatures of 330 to 34 were obtained from these pellets using an injection molding machine (N-65 manufactured by Nippon Steel Co., Ltd.).
An IC tray was molded at 0 ° C. and a mold temperature of 130 ° C., and the releasing effect of each composition was examined. The mold release effect is the number of injection molding shots (limit number) until the mold release effect disappears due to mold deposit, etc.
Evaluated by Further, the appearance of the molded product was visually observed. The results are shown in Table 1.

【0018】比較例1〜6 表1に示す配合の芳香族ポリスルホン成形用組成物を調
製した。比較例2および3は実施例1と同様にETFE
を溶融ブレンドし、比較例5および6は実施例1のET
FEを低分子量PTFE(ダイキン工業(株)製ルブロ
ンL−5F)に代えた他は同様の方法で配合した。
Comparative Examples 1 to 6 Aromatic polysulfone molding compositions having the formulations shown in Table 1 were prepared. Comparative Examples 2 and 3 have the same ETFE as Example 1.
Are melt-blended and Comparative Examples 5 and 6 are ET of Example 1.
Compounding was carried out in the same manner except that FE was replaced with low molecular weight PTFE (Lubron L-5F manufactured by Daikin Industries, Ltd.).

【0019】えられたペレットを用い実施例1と同様に
してICトレイを射出成形し、離型効果および外観を調
べた。結果を表1に示す。
Using the obtained pellets, an IC tray was injection-molded in the same manner as in Example 1 and the releasing effect and appearance were examined. The results are shown in Table 1.

【0020】[0020]

【表1】 [Table 1]

【0021】[0021]

【発明の効果】本発明によれば、芳香族ポリスルホンの
成形性、特に成形時の流動性、モールドデポジット、離
型性を改善することができる。
According to the present invention, the moldability of the aromatic polysulfone, especially the fluidity at the time of molding, the mold deposit, and the releasability can be improved.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 芳香族ポリスルホン100 重量部に対し、
エチレン−テトラフルオロエチレン共重合体0.3 〜5重
量部とカーボン系繊維または粉末0〜25重量部が配合さ
れてなる芳香族ポリスルホン成形用組成物。
1. To 100 parts by weight of aromatic polysulfone,
An aromatic polysulfone molding composition comprising 0.3 to 5 parts by weight of an ethylene-tetrafluoroethylene copolymer and 0 to 25 parts by weight of carbon fiber or powder.
JP12192992A 1992-05-14 1992-05-14 Aromatic polysulfone molding composition Expired - Fee Related JP3152255B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12192992A JP3152255B2 (en) 1992-05-14 1992-05-14 Aromatic polysulfone molding composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12192992A JP3152255B2 (en) 1992-05-14 1992-05-14 Aromatic polysulfone molding composition

Publications (2)

Publication Number Publication Date
JPH05311074A true JPH05311074A (en) 1993-11-22
JP3152255B2 JP3152255B2 (en) 2001-04-03

Family

ID=14823426

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12192992A Expired - Fee Related JP3152255B2 (en) 1992-05-14 1992-05-14 Aromatic polysulfone molding composition

Country Status (1)

Country Link
JP (1) JP3152255B2 (en)

Also Published As

Publication number Publication date
JP3152255B2 (en) 2001-04-03

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