JPH03215560A - Resin composition - Google Patents

Resin composition

Info

Publication number
JPH03215560A
JPH03215560A JP1064990A JP1064990A JPH03215560A JP H03215560 A JPH03215560 A JP H03215560A JP 1064990 A JP1064990 A JP 1064990A JP 1064990 A JP1064990 A JP 1064990A JP H03215560 A JPH03215560 A JP H03215560A
Authority
JP
Japan
Prior art keywords
polyether sulfone
resin composition
resin
magnesium carbonate
parts
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
JP1064990A
Other languages
Japanese (ja)
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 JP1064990A priority Critical patent/JPH03215560A/en
Publication of JPH03215560A publication Critical patent/JPH03215560A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain a resin composition which is less corrosive to the mold or the like during molding and prevented from forming a corrosive gas which adversely affects the mold by adding magnesium carbonate to a polyether sulfone resin. CONSTITUTION:0.01-20 pts.wt., desirably 0.1-10 pts.wt. magnesium carbonate is added to 100 pts.wt. polyether sulfone resin to obtain a heat-resistant resin composition which can be used for electrical and electronic components.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、ポリエーテスルホン樹脂に炭酸マグネシウム
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ボリエーテルスルホン樹脂組成
物に関する.〔従来の技術とその問題点〕 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、電子部品の信転性
を低下せしめる結果となっている.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. 〔問題点を解決するための手段〕 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
への炭酸マグネシウムの添加が脊効であることを見出し
本発明を完成した.すなわち、本発明はポリエーテルス
ルホン樹脂100重量部に対して炭酸マグネシウム0.
01〜20重量部を添加することを特徴とする樹脂組成
物である. 本発明で使用されるポリエーテルスルホン樹脂とは、ア
ルカリフェノレート基と、電子吸引性スルホン基で活性
化された芳香族ハロゲン蟇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
スルホン結合の王者を必須の結合単位とする線状重合体
である。
[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a heat-resistant resin molding material characterized by adding magnesium carbonate to polyethersulfone resin, and more specifically, This article relates to a polyether sulfone resin composition that can reduce corrosion of molds, etc. [Prior art and its problems] Polyether sulfone resin has excellent mechanical, thermal, and electrical properties, so it is molded using various molding methods and used for mechanical parts, electrical parts, etc. Widely used in 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 temperatures above 100°C, corrosive gases will be generated and metal parts will be corroded.Especially when used in the electrical and electronic fields, corrosive gases such as sulfur dioxide gas will be generated. This results in a decrease in the reliability of electronic components.In the past, attempts have been made to add zinc oxide, etc. to prevent the adverse effects of corrosive gases generated from resins, but no sufficient effect has been obtained. As a result, its use as a molding material and molded product is limited. [Means for solving the problem] In order to prevent the adverse effects of corrosive gas on molded products, the inventors of the present invention As a result of various studies, they discovered that the addition of magnesium carbonate to polyether sulfone resin was effective and completed the present invention.That is, the present invention is based on the addition of 0.0 parts by weight of magnesium carbonate to 100 parts by weight of polyether sulfone resin.
01 to 20 parts by weight of the resin composition. The polyether sulfone resin used in the present invention is a type obtained by a condensation reaction between an alkali phenolate group and an aromatic halogen resin activated with an electron-withdrawing sulfone group in an aprotic polar solvent. It is a linear polymer whose essential bonding units are 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. (1) −(一〇−■−SO2一■一)一 (3) −(−0べ!トSO 2べ臣FOべ亜xO−◇X)−(
5) ( o−(SトS O r(リ−0−(夛ヘ互刈)−(
6) 一(一(ト)〈■トS O 2べ歪Σ《Sトs02べ巨
トoべ巨と)(7) ?{’− 0−<り−SO2べ至トO−(Σh C H
 2−■→一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42−7799
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. また本発明で用いられる炭酸マグネシウムは、通常(M
gCO3)という化学組成であり、天然にはマグネサイ
トとして産出される。また、mMgco■・nMg (
OH) z  ・xH20の様な構造の塩基性塩も炭酸
マグネシウムに含まれる。
For example, the following structure is a very typical example. (1) -(10-■-SO21■1)1(3) -(-0be!TOSO 2beishinFOBeaxO-◇X)-(
5)
6) One (one (to)〈■toSO 2be distortion Σ《Stos02be huge obe huge and) (7) ? {'- 0-<ri-SO2beto O-(Σh C H
2-■→1 These polyether sulfone resins are disclosed in, for example, Japanese Patent Publication No. 40-10067 and Japanese Patent Publication No. 42-7799.
It can be easily produced by the method described in Japanese Patent Publication No. 47-617. Further, magnesium carbonate used in the present invention is usually (M
It has a chemical composition of gCO3) and is naturally produced as magnesite. In addition, mMgco■・nMg (
Basic salts with structures such as OH) z ・xH20 are also included in magnesium carbonate.

本発明における炭酸マグネシウム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。
The amount of magnesium carbonate added in the present invention is 0.01 to 20 parts by weight, preferably 0.1 to 10 parts by weight, per 100 parts by weight of the polyethersulfone resin.

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. 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
成形材料はベレットとして使用するのが好ましい.次い
で該ベレント等は射出成形機等の成形機により成形する
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. The polyethersulfone resin according to the present invention is generally molded as follows. Polyether sulfone resin and additives are mixed using a mixer such as a Henschel mixer, and then kneaded using a hot roll, extruder, etc. to form a molding material. This molding material is preferably used as a pellet. Next, the berent or the like is molded using a molding machine such as an injection molding machine.

本発明では上記ポリエーテルスルホン樹脂成形材料に必
要に応じ、タルク、マイ力、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、セラミッ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組成物
の品質を損なわない範囲で混和しても良い. 〔実施例〕 以下、実施例により本発明を詳細に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。
In the present invention, fillers such as talc, Myriki, and glass beads may be added to the polyether sulfone resin molding material, if necessary.
Various additives such as glass fibers, carbon fibers, potassium titanate fibers, aramid fibers, ceramic fibers, etc., stabilizers, ultraviolet absorbers, colorants, mold release agents, etc. may impair the quality of the resin composition. They may be mixed as long as they are not mixed. [Examples] Hereinafter, the present invention will be explained 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
S3600P (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、ヘンシエルミキサーでドライブレンドした。
Examples 1 to 4 and Comparative Examples 1 to 3 VICTREX PE as polyether sulfone resin
S3600P (trademark, Imperial Chemical Industries Ltd., UK) powder and various additives were blended in the proportions shown in Table 1, and dry blended 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、均一なベレント状の成形材料
を得た. 該ベレ,トを第1図に示すごとくガラス容器に鋼材と共
に10gいれ、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。
This mixture was extruded using a twin-screw extruder at a cylinder temperature of 320°C.
It was extruded at ~350°C to obtain a uniform berent-like molding material. As shown in FIG. 1, 10 g of the bellet and steel material were placed in a glass container, 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Ml値)より判断した。ま
た、さらに上記のペレノトにつきシリンダ温度330〜
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10g入れ、中に5
X5mmO銅箔を吊して、150゜Cの高温槽中に10
0時間静直し銅箔の変色程度を観察して表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 Ml value) in accordance with JIS K7210. Furthermore, the cylinder temperature is 330~
Injection molding was carried out at 360°C. Crush the molded product, put 10g into an Erlenmeyer flask as shown in Figure 2, and put 5.
X5mmO copper foil was suspended in a high temperature bath at 150°C for 10 minutes.
After standing still for 0 hours, the degree of discoloration of the copper foil was observed, 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 1: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 1: Slight discoloration 0: No discoloration It was shown more.

〔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1ヒに効果があるため
、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、本発明の意義は大きい。
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, making it possible to reduce maintenance costs for molds and molding machines during injection molding and extrusion molding. .. Further, various molded products made of the polyether sulfone resin of the present invention can be used for electrical and electronic parts because the generation of corrosive gases is suppressed, and the present invention is of great significance.

4.図面の説明 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,ト状成形材料(試料)を使用し表1 ?gCOff   ・・・.iΦコ1巳イピt)對Iし
ζdこづ≧ぎ111Vム(4MgCO,.一g (OH
)2.511■0)ZnO     ・・・・毎Φj■
三イピt)とオ七kテA;≦〉11E♂冒一M1i11
!IfJs牛  虐μ定=  320゜C荷重:  2
.16kg 表2 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:鋼材 を示す. 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。
4. Explanation of the Drawings Figure 1 shows a sample using a pellet-shaped molding material (sample) obtained from a polyethersulfone resin composition. gCoff... 111V (4MgCO, .1g (OH
)2.511■0) ZnO...every Φj■
3 Ipi t) and O 7 k Te A;
! IfJs Cow Cruelty = 320°C Load: 2
.. 16kg Table 2 This is a schematic diagram showing the discoloration test of steel materials, each number is 1
: Metal can 2: Metal can 3: Sample 4: Steel material. 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重量部に対して炭酸マ
グネシウム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 magnesium carbonate is added to 100 parts by weight of the polyethersulfone resin.
JP1064990A 1990-01-22 1990-01-22 Resin composition Pending JPH03215560A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1064990A JPH03215560A (en) 1990-01-22 1990-01-22 Resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1064990A JPH03215560A (en) 1990-01-22 1990-01-22 Resin composition

Publications (1)

Publication Number Publication Date
JPH03215560A true JPH03215560A (en) 1991-09-20

Family

ID=11756070

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1064990A Pending JPH03215560A (en) 1990-01-22 1990-01-22 Resin composition

Country Status (1)

Country Link
JP (1) JPH03215560A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0727456A1 (en) * 1995-02-16 1996-08-21 Sumitomo Chemical Company, Limited Aromatic polysulfone resin composition

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62131062A (en) * 1985-12-03 1987-06-13 Mitsui Toatsu Chem Inc Platable resin composition having excellent heat transfer characteristic
JPS62241390A (en) * 1986-04-11 1987-10-22 住友化学工業株式会社 Printed wiring board
JPS63178166A (en) * 1987-01-16 1988-07-22 Sumitomo Chem Co Ltd Aromatic polysulfone resin composition
JPH01301756A (en) * 1987-03-24 1989-12-05 Sumitomo Chem Co Ltd Aromatic polysulfone resin composition having excellent plating characteristic

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62131062A (en) * 1985-12-03 1987-06-13 Mitsui Toatsu Chem Inc Platable resin composition having excellent heat transfer characteristic
JPS62241390A (en) * 1986-04-11 1987-10-22 住友化学工業株式会社 Printed wiring board
JPS63178166A (en) * 1987-01-16 1988-07-22 Sumitomo Chem Co Ltd Aromatic polysulfone resin composition
JPH01301756A (en) * 1987-03-24 1989-12-05 Sumitomo Chem Co Ltd Aromatic polysulfone resin composition having excellent plating characteristic

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0727456A1 (en) * 1995-02-16 1996-08-21 Sumitomo Chemical Company, Limited Aromatic polysulfone resin composition

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