JPH03199264A - Resin composition - Google Patents

Resin composition

Info

Publication number
JPH03199264A
JPH03199264A JP33662289A JP33662289A JPH03199264A JP H03199264 A JPH03199264 A JP H03199264A JP 33662289 A JP33662289 A JP 33662289A JP 33662289 A JP33662289 A JP 33662289A JP H03199264 A JPH03199264 A JP H03199264A
Authority
JP
Japan
Prior art keywords
alumina
polyether sulfone
pts
resin
bonds
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
JP33662289A
Other languages
Japanese (ja)
Other versions
JP2667723B2 (en
Inventor
Masami Amano
正己 天野
Yoshihisa Goto
善久 後藤
Toshiaki Takahashi
敏明 高橋
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP1336622A priority Critical patent/JP2667723B2/en
Publication of JPH03199264A publication Critical patent/JPH03199264A/en
Application granted granted Critical
Publication of JP2667723B2 publication Critical patent/JP2667723B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To provide a polyether sulfone resin composition depressed in the generation of corrositive gases in the molding processing of the resin to reduce the corrosion of molds and capable of being employed for electric and electronic parts by adding gamma-alumina to a polyether sulfone resin. CONSTITUTION:(A) 100 pts.wt. of a polyether sulfone resin, a linear polymer, having arylene bonds, ether bonds and sulfone bonds as essential bond units is compounded with (B) 0.01-20 pts.wt., preferably 0.1-10 pts.wt., of gamma-alumina, an intermediate alumina or alumina anhydride, prepared by dehydrating alumina hydrate and further, if necessary, with a filler such as talc or mica, a fibrous reinforcing material such as glass fibers or carbon fibers, a stabilizer, an UV ray absorbent, etc., followed by mixing with a Henschel mixer, etc., and kneading with an extruder to provide a molding material.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、ポリエーテルスン樹脂にT−アルミナを添加
することを特徴とする耐熱性樹脂成形材料に関するもの
であり、さらに詳しくは成形加工時の金型等の腐食を減
じることが可能なポリエーテルスルホン樹脂#Ji底物
に関する。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a heat-resistant resin molding material characterized by adding T-alumina to polyethersun resin, and more specifically, This invention relates to a polyether sulfone resin #Ji sole that can reduce corrosion of molds, etc.

〔従来の技術とその問題点〕[Conventional technology and its problems]

ポリエーテルスルホン樹脂は機械的性質、熱的性質、電
気的性質などに優れた性能を有しているため、各種の成
形法により成形されて、機械部品、電気電子部品等に広
く利用されている。 しかしながら、ポリエーテルスル
ホン樹脂の加工温度は340〜400°Cとかなりの高
温であり、このような高温下においては若干の金属腐食
性ガスを発生するため、成形加工時には金型や成形機を
腐食させたり、成形品を100°C以上でエージング処
理すると腐食性ガスが発生し金属部分が腐食されるとい
う問題が生じる。特に電気電子分野で使用する場合、亜
硫酸ガス等の腐食性ガスの発生により、電子部品の信頼
性を低下せしめる結果となっている。
Polyether sulfone resin has excellent mechanical, thermal, and electrical properties, so it is molded using various molding methods and is widely used in mechanical parts, electrical and electronic parts, etc. . However, the processing temperature of polyether sulfone resin is quite high at 340 to 400°C, and at such high temperatures some metal corrosive gas is generated, which can corrode the mold and molding machine during the molding process. If molded products are aged at 100° C. or higher, corrosive gases are generated and metal parts are corroded. Particularly when used in the electrical and electronic fields, the reliability of electronic components is reduced due to the generation of corrosive gases such as sulfur dioxide gas.

従来、樹脂よりの腐食性ガスの発生による悪影響を防ぐ
ために、酸化亜鉛等の添加が試みられているが、充分な
効果が得られないため、成形材料及び成形品としての用
途が制限されている状況にある。
In the past, attempts have been made to add zinc oxide, etc. to prevent the negative effects of corrosive gases generated from resins, but as sufficient effects cannot be obtained, their use as molding materials and molded products is limited. situation.

〔問題点を解決するための手段〕[Means for solving problems]

ここで本発明者らは成形品の腐食性ガスの悪影響を防止
すべく、種々研究した結果、ポリエーテルスルホン樹脂
へのT−アルミナの添加が有効であることをみいだし本
発明を完成した。
In order to prevent the adverse effects of corrosive gases on molded products, the inventors of the present invention have conducted various studies and have found that the addition of T-alumina to polyether sulfone resin is effective, and have completed the present invention.

すなわち、本発明はポリエーテルスルホン樹脂100 
!i量部に対してT−アルミナ0.01〜20重量部を
添加することを特徴とする樹脂&Itc物である。
That is, the present invention uses polyether sulfone resin 100
! It is a resin & Itc product characterized by adding 0.01 to 20 parts by weight of T-alumina to i parts.

本発明で使用されるポリエーテルスルホン樹脂とは、ア
ルカリフェルレート基と、電子吸引性スルホン基で活性
化された芳香族ハロゲン基と非プロトン性極性溶媒中で
縮合反応させることにより得られる形式の重合体であり
、アリーレン結合(芳香族結合)、エーテル結合および
スルホン結合の三者を必須の結合単位とする線状重合体
である。
The polyether sulfone resin used in the present invention is a type obtained by a condensation reaction between an alkali ferulate group and an aromatic halogen group activated with an electron-withdrawing sulfone group in an aprotic polar solvent. It is a linear polymer that has three essential bonding units: arylene bonds (aromatic bonds), ether bonds, and sulfone bonds.

例えばきわめて代表的な例として次のような構造のもの
が挙げられる。
For example, the following structure is a very typical example.

(1)  −(−0−O−S(h−■−)−CHコ (2)  へ(−0−■−5Ovo−0−o−C−■−
)−Hz (3)  −(−0−O−SOa−■−0−■−0−■
−)−Hs (4)  −(−□−■−S Oz −0−■−0−■
−C−00−)−Hi (5) −(−〇−■−502−■−0−O−■−)−(6) −(−o−O−s02−■−■−5O2−■−0−00
−)−(7)  1−o−O−so2−■−o−O−c
 H2−■−)−これらのポリエーテルスルホン樹脂は
、例えば特公昭40−10067号、特公昭42−77
99号および特公昭47−617号等に記載の方法によ
って容易に製造できる。
(1) -(-0-O-S(h-■-)-CH ko(2) To(-0-■-5Ovo-0-o-C-■-
)-Hz (3) -(-0-O-SOa-■-0-■-0-■
-)-Hs (4) -(-□-■-S Oz -0-■-0-■
-C-00-)-Hi (5) -(-〇-■-502-■-0-O-■-)-(6) -(-o-O-s02-■-■-5O2-■- 0-00
-) -(7) 1-o-O-so2-■-o-O-c
H2-■-)-These polyether sulfone resins are disclosed in, for example, Japanese Patent Publication No. 40-10067 and Japanese Patent Publication No. 42-77.
It can be easily produced by the method described in Japanese Patent Publication No. 99 and Japanese Patent Publication No. 47-617.

また本発明で用いられるγ−アルミナとは、中間アルミ
ナ又は無水アルミナを意味するものであり、例えば、ρ
・χ・η・δ・θ型等の結晶構造をもつアルミナが挙げ
られ2、これらはアル藁す水和物の脱水によって生じ、
さらに高温で焼成することによって最も安定なα−アル
ミナへと変化する0本発明におけるr−アルミナの添加
量はポリエーテルスルホン樹脂100重量部に対して0
.01〜20重量部、好ましくは0.1〜10重量部で
ある。添加量が少なすぎると腐食性ガスの低減効果が殆
ど見られず、逆に20重量部を越えて使用する場合は腐
食性ガスの低減効果は充分であるが、流動性が低下し成
形加工性に問題が生ずる為、好ましくない。
Furthermore, γ-alumina used in the present invention means intermediate alumina or anhydrous alumina, such as ρ-alumina.
・There are aluminas with crystal structures such as χ, η, δ, and θ types2, which are produced by dehydration of aluminum hydrates,
Further, by firing at a high temperature, it changes to the most stable α-alumina.The amount of r-alumina added in the present invention is 0 to 100 parts by weight of the polyethersulfone resin.
.. 0.1 to 20 parts by weight, preferably 0.1 to 10 parts by weight. If the amount added is too small, there will be almost no effect of reducing corrosive gases.On the other hand, if it is used in excess of 20 parts by weight, the effect of reducing corrosive gases will be sufficient, but the fluidity will decrease and the moldability will be affected. This is not desirable because it causes problems.

本発明によるポリエーテルスルホン樹脂は通常次ぎのよ
うにして成形する。ポリエーテルスルホン樹脂と添加剤
とをヘンシェルミキサー等の混合機で混合し、さらに熱
ロール、押出機等により混練して成形材料にする。この
成形材料はペレットとして使用するのが好ましい0次い
で該ペレット等は射出底形機等の成形機により成形する
The polyethersulfone resin according to the present invention is generally molded as follows. The polyether sulfone resin and additives are mixed with a mixer such as a Henschel mixer, and then kneaded with a hot roll, extruder, etc. to form a molding material. This molding material is preferably used in the form of pellets.Then, the pellets are molded using a molding machine such as an injection bottom molding machine.

本発明では上記ポリエーテルスルホン樹脂酸形材料に必
要に応じ、タルク、マイカ、カラスビーズ等の充填剤、
ガラス繊維、炭素繊維、チタン酸カリ繊維、アラミド繊
維、セラ旦ツク質繊維等の繊維状強化材、安定剤、紫外
線吸収剤、着色剤、離型剤等の各種添加剤を樹脂s;u
tc物の品質を損なわない範囲で混和しても良い。
In the present invention, if necessary, fillers such as talc, mica, and glass beads are added to the polyether sulfone resin acid type material.
Various additives such as glass fibers, carbon fibers, potassium titanate fibers, aramid fibers, ceramic fibers, etc., stabilizers, ultraviolet absorbers, colorants, and mold release agents are added to the resin.
They may be mixed as long as the quality of the tc material is not impaired.

〔実施例〕〔Example〕

以下、実施例により本発明の詳細な説明するがこれらは
単なる例示であり、本発明はこれに限定されるものでは
ない。
Hereinafter, the present invention will be described in detail with reference to Examples, but these are merely illustrative and the present invention is not limited thereto.

実施例1〜4および比較例1〜3 ポリエーテルスルホン樹脂としてVICTREX PE
53600P (商標、英国インペリアルケミカルイン
ダストリー社)パウダーと各種添加剤を表1に示す割合
で配合し、ヘンシェルくキサ−でトライブレンドした。
Examples 1 to 4 and Comparative Examples 1 to 3 VICTREX PE as polyether sulfone resin
53600P (trademark, Imperial Chemical Industries Ltd., UK) powder and various additives were blended in the proportions shown in Table 1 and triblended using a Henschel mixer.

この混合物を二軸押出機を用いてシリンダー温度320
〜350°Cで押しだし、均一なペレット状の成形材料
を得た。
This mixture was extruded using a twin-screw extruder at a cylinder temperature of 320°C.
A uniform pellet-shaped molding material was obtained by extrusion at ~350°C.

該ペレットを第1図に示すごとくガラス容器に鋼材と共
に10g入れ、380°Cで24時間加熱してその鋼材
の変色の程度を観察した。
10 g of the pellets were placed in a glass container together with a steel material as shown in FIG. 1, heated at 380° C. for 24 hours, and the degree of discoloration of the steel material was observed.

また、各サンプルの流動性はJIS K7210に準拠
しメルトインデックス(以下MI値)より判断した。 
また、さらに上記のペレットにつきシリンダー温度33
0〜360°Cで射出成形を行った。該成形品を粉砕し
、第2図に示すごとく、三角フラスコにlOg入れ、中
に5 X 5 mmO銅箔を吊して、150℃の高温槽
中に100時間靜置装銅箔の変色程表1 α−アルミナ・・・純正化学株式会社品ZnO・・ ・
番屯j1三イヒ!1シ1づ1jjこ$M1濱1耘ヒ穿d
牛  沼彰定・ ・ ・ 320°C荷重・・・2.1
6kg 表2 度を観察して、表2のような結果を得た。
Further, the fluidity of each sample was determined based on the melt index (hereinafter referred to as MI value) in accordance with JIS K7210.
Furthermore, the cylinder temperature is 33 for the above pellets.
Injection molding was performed at 0-360°C. The molded product was crushed, and as shown in Fig. 2, 10 g was placed in an Erlenmeyer flask, with a 5 x 5 mmO copper foil suspended therein, and placed in a high-temperature bath at 150°C for 100 hours to prevent discoloration of the copper foil. Table 1 α-Alumina...Junsei Kagaku Co., Ltd. product ZnO...
Banton J1 Sanihi! 1shi1zu1jjko$M1hama1耘hi d
Akisada Ushinuma・・・320°C load・・・2.1
6kg Table 2 Observation was made and the results shown in Table 2 were obtained.

尚、表1及び表2に示す変色の判定基準は3:変色大 2:かなり変色 l:わずかに変色 0:変色なし より示した。The criteria for discoloration shown in Tables 1 and 2 are 3: Severe discoloration. 2: Significant discoloration l: Slight discoloration 0: No discoloration More shown.

〔発明の効果〕〔Effect of the invention〕

本発明によるポリエーテルスルホン樹脂成形材料は、腐
食性ガスの発生による悪影響の防止に効果があるため、
射出成形、押出成形時の成形金形、成形機の保守コスト
の低下が可能となる。 また、本発明のポリエーテルス
ルホン樹脂で成形された各種成形品は、腐食性ガスの発
生が抑制されるため電気電子部品への使用が可能となり
、本発第1図はポリエーテルスルホン樹脂組成物よりえ
られたペレット状成形材料(試料)を使用し鋼材の変色
試験を示す概略図であり、各数字は各々 1:金属缶 
2:金属缶 3:試料4:tg4材 を示す。
The polyether sulfone resin molding material according to the present invention is effective in preventing the adverse effects caused by the generation of corrosive gases.
It is possible to reduce maintenance costs for molds and molding machines during injection molding and extrusion molding. In addition, various molded products molded with the polyether sulfone resin of the present invention can be used for electrical and electronic parts because the generation of corrosive gas is suppressed. It is a schematic diagram showing a discoloration test of steel materials using a pellet-shaped molding material (sample) obtained from the above, and each number is 1: Metal can.
2: Metal can 3: Sample 4: TG4 material.

第2図も同じく試料による銅箔の変色試験を示す概略図
であり、各数字は 各々 1:三角フラスコ 2:シリ
コン栓 3:試料 4:銅箔を示す。
FIG. 2 is also a schematic diagram showing a discoloration test of copper foil using a sample, and each number indicates 1: Erlenmeyer flask, 2: silicon stopper, 3: sample, and 4: copper foil.

Claims (1)

【特許請求の範囲】[Claims] ポリエーテルスルホン樹脂100重量部に対してγ−ア
ルミナ0.01〜20重量部を添加することを特徴とす
るポリエーテルスルホン樹脂組成物。
A polyethersulfone resin composition characterized in that 0.01 to 20 parts by weight of γ-alumina is added to 100 parts by weight of the polyethersulfone resin.
JP1336622A 1989-12-27 1989-12-27 Resin composition Expired - Lifetime JP2667723B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1336622A JP2667723B2 (en) 1989-12-27 1989-12-27 Resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1336622A JP2667723B2 (en) 1989-12-27 1989-12-27 Resin composition

Publications (2)

Publication Number Publication Date
JPH03199264A true JPH03199264A (en) 1991-08-30
JP2667723B2 JP2667723B2 (en) 1997-10-27

Family

ID=18301057

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1336622A Expired - Lifetime JP2667723B2 (en) 1989-12-27 1989-12-27 Resin composition

Country Status (1)

Country Link
JP (1) JP2667723B2 (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62240353A (en) * 1986-04-10 1987-10-21 Idemitsu Kosan Co Ltd Molding resin composition

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62240353A (en) * 1986-04-10 1987-10-21 Idemitsu Kosan Co Ltd Molding resin composition

Also Published As

Publication number Publication date
JP2667723B2 (en) 1997-10-27

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