JP2683437B2 - Resin composition - Google Patents
Resin compositionInfo
- Publication number
- JP2683437B2 JP2683437B2 JP1336621A JP33662189A JP2683437B2 JP 2683437 B2 JP2683437 B2 JP 2683437B2 JP 1336621 A JP1336621 A JP 1336621A JP 33662189 A JP33662189 A JP 33662189A JP 2683437 B2 JP2683437 B2 JP 2683437B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- present
- weight
- polyether sulfone
- resin composition
- 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
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- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、ポリエーテルスルホン樹脂にアルミナ水和
物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組
成物に関する。TECHNICAL FIELD The present invention relates to a heat-resistant resin molding material characterized by adding an alumina hydrate to a polyether sulfone resin, and more specifically to a molding process. The present invention relates to a polyether sulfone resin composition capable of reducing corrosion of a mold or the like at the time.
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℃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℃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。Polyethersulfone resin has mechanical properties, thermal properties,
Since it has excellent properties such as electrical properties, it is molded by various molding methods and widely used for mechanical parts, electric and electronic parts, and the like. However, the processing temperature of polyethersulfone resin is a fairly high temperature of 340-400 ° C, and a slight amount of metal corrosive gas is generated under such high temperature. Alternatively, if the molded product is aged at 100 ° C. or higher, a corrosive gas is generated and the metal part is corroded. In particular, when used in the field of electric and electronic equipment, the generation of corrosive gas such as sulfurous acid gas results in a decrease in the reliability of electronic components.
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。Conventionally, in order to prevent adverse effects due to generation of corrosive gas from resin, addition of zinc oxide or the like has been attempted, but since sufficient effects cannot be obtained, applications as molding materials and molded articles are limited. In the situation.
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
脂へのアルミナ水和物の添加が有効であることを見出し
本発明を完成した。Here, as a result of various studies, the present inventors have found that the addition of alumina hydrate to the polyethersulfone resin is effective, and completed the present invention.
すなわち、本発明は下記式(1)〜(7)で表される
構造単位より選ばれたポリエーテルスルホン樹脂100重
量部に対して、A12O3・3H2O、A12O3・H2O、またはA1(O
H)3の化学式で表されるアルミナ水和物0.1重量部以上、
10重量部を越えない量を添加して得られることを特徴と
するポリエーテルスルホン樹脂組成物である。That is, the present invention is based on 100 parts by weight of a polyether sulfone resin selected from structural units represented by the following formulas (1) to (7), A1 2 O 3 .3H 2 O, A1 2 O 3 .H 2 O, or A1 (O
H) 3 or more alumina hydrate represented by the chemical formula of 3 0.1 parts by weight or more,
A polyethersulfone resin composition, which is obtained by adding an amount not exceeding 10 parts by weight.
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。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。 The polyether sulfone resin used in the present invention,
An alkali phenolate group, an aromatic halogen group activated with an electron-withdrawing sulfone group, and a polymer obtained by a condensation reaction in an aprotic polar solvent, wherein the arylene bond (aromatic bond), It is a linear polymer having an ether bond and a sulfone bond as essential bonding units. For example, a very typical example is one having the following structure.
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。 These polyether sulfone resins are, for example,
It can be easily produced by the method described in JP-B-40-10067, JP-B-42-7799 and JP-B-47-617.
また本発明で用いられるアルミナ水和物とは一般に
[AL2O3・nH2O]という化学組成の化合物であり、例え
ば(AL2O3・3H2O)、(AL2O3・H2O)等があり、さらに
は水酸化アルミニウム[AL(OH)3]もこれに含まれる。The alumina hydrate used in the present invention is generally a compound having a chemical composition of [AL 2 O 3 · nH 2 O], such as (AL 2 O 3 · 3 H 2 O), (AL 2 O 3 · H 2 O) and aluminum hydroxide [AL (OH) 3 ] is also included in this.
本発明におけるアルミナ水和物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。The amount of the alumina hydrate added in the present invention is 0.01 to 20 parts by weight, preferably 0.1 to 10 parts by weight, based on 100 parts by weight of the polyether sulfone resin. If the amount added is too small, the effect of reducing corrosive gas is scarcely seen, and conversely, when used in excess of 20 parts by weight, the effect of reducing corrosive gas is sufficient, but the fluidity decreases and moldability becomes poor. It is not preferable 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。次
いで該ペレット等は射出成形機等の成形機により成形す
る。The polyethersulfone resin according to the present invention is usually molded as follows. The polyethersulfone resin and the additive are mixed by a mixer such as a Henschel mixer, and further kneaded by a hot roll, an extruder or the like to form a molding material. This molding material is preferably used as pellets. Next, the pellets and the like are formed by 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。In the present invention, if necessary for the polyether sulfone resin molding material, filler such as talc, mica, crow beads, glass fiber, carbon fiber, potassium titanate fiber, aramid fiber, fibrous reinforcing material such as ceramic fiber, Stabilizer,
Various additives such as an ultraviolet absorber, a coloring agent, and a release agent may be mixed as long as the quality of the resin composition is not impaired.
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。Hereinafter, the present invention will be described in detail with reference to examples, but these are merely examples, 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 PES3600P
(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
シェルミキサーでドライブレンドした。この混合物を二
軸押出機を用いてシリンダー温度320〜350℃で押出し、
均一なペレット状の成形材料を得た。Examples 1-4 and Comparative Examples 1-3 VICTREX PES3600P as a polyether sulfone resin
(Trademark, Imperial Chemical Industry, UK)
The powder and various additives were blended in the proportions shown in Table 1 and dry blended with a Henschel mixer. This mixture is extruded using a twin-screw extruder at a cylinder temperature of 320 to 350 ° C,
A uniform pellet-like molding material was obtained.
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℃で24時間加熱してその鋼材の変色の
程度を観察した。As shown in FIG. 1, 10 g of the pellet was put in a glass container together with a steel material, and heated at 380 ° C. for 24 hours to observe the degree of discoloration of the steel material.
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330〜360℃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5×5mmの銅箔を吊して、150℃の高温
槽中に100時間静置し銅箔の変色程度を観察して、表2
のような結果を得た。The fluidity of each sample was determined from the melt index (hereinafter, MI value) in accordance with JIS K7210. Further, the above pellets were subjected to injection molding at a cylinder temperature of 330 to 360 ° C. The molded product was crushed and, as shown in FIG. 2, an Erlenmeyer flask. Put 10g in a cup, hang a 5 x 5mm copper foil in it, and let it stand in a high temperature tank at 150 ° C for 100 hours to observe the degree of discoloration of the copper foil.
I got a result like.
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 the discoloration shown in Tables 1 and 2 are as follows: 3: large discoloration 2: considerable discoloration 1: slight discoloration 0: no discoloration
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、本発明の意義は大きい。Polyether sulfone resin molding material according to the present invention,
Since it is effective in preventing adverse effects due to the generation of corrosive gas, it is possible to reduce the maintenance cost of the molding die and the molding machine at the time of injection molding and extrusion molding. In addition, various molded articles molded with the polyethersulfone resin of the present invention can be used for electric and electronic parts because generation of corrosive gas is suppressed, and the present invention is significant.
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: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。FIG. 1 is a schematic diagram showing a discoloration test of a steel material using a pellet-shaped molding material (sample) obtained from a polyethersulfone resin composition, where the numbers are respectively 1: metal can, 2: metal can,
3: Sample, 4: Steel material is shown. FIG. 2 is also a schematic diagram showing a discoloration test of a copper foil by a sample, where each number is 1: Erlenmeyer flask, 2: Silicon stopper,
3: Sample, 4: Copper foil is shown.
Claims (1)
より選ばれたポリエーテルスルホン樹脂100重量部に対
して、A12O3・3H2O、A12O3・H2O、またはA1(OH)3の化学
式で表されるアルミナ水和物0.1重量部以上、10重量部
を越えない量を添加して得られることを特徴とするポリ
エーテルスルホン樹脂組成物。 1. A1 2 O 3 .3H 2 O, A1 2 O 3 .H based on 100 parts by weight of a polyether sulfone resin selected from structural units represented by the following formulas (1) to (7). A polyether sulfone resin composition obtained by adding an amount of 0.1 parts by weight or more and not more than 10 parts by weight of an alumina hydrate represented by the chemical formula of 2 O or A1 (OH) 3 .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1336621A JP2683437B2 (en) | 1989-12-27 | 1989-12-27 | Resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1336621A JP2683437B2 (en) | 1989-12-27 | 1989-12-27 | Resin composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03199263A JPH03199263A (en) | 1991-08-30 |
JP2683437B2 true JP2683437B2 (en) | 1997-11-26 |
Family
ID=18301047
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1336621A Expired - Lifetime JP2683437B2 (en) | 1989-12-27 | 1989-12-27 | Resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2683437B2 (en) |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60249207A (en) * | 1984-05-23 | 1985-12-09 | 株式会社東海理化電機製作所 | Molding material for electric part |
JPS62240353A (en) * | 1986-04-10 | 1987-10-21 | Idemitsu Kosan Co Ltd | Molding resin composition |
-
1989
- 1989-12-27 JP JP1336621A patent/JP2683437B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH03199263A (en) | 1991-08-30 |
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