JPH03199263A - Resin composition - Google Patents
Resin compositionInfo
- Publication number
- JPH03199263A JPH03199263A JP33662189A JP33662189A JPH03199263A JP H03199263 A JPH03199263 A JP H03199263A JP 33662189 A JP33662189 A JP 33662189A JP 33662189 A JP33662189 A JP 33662189A JP H03199263 A JPH03199263 A JP H03199263A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- pts
- polyether sulfone
- bonds
- alumina hydrate
- 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
Links
- 239000011342 resin composition Substances 0.000 title claims abstract description 5
- 239000011347 resin Substances 0.000 claims abstract description 20
- 229920005989 resin Polymers 0.000 claims abstract description 20
- 229920006393 polyether sulfone Polymers 0.000 claims abstract description 19
- 239000004695 Polyether sulfone Substances 0.000 claims abstract description 18
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 7
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims abstract description 3
- 239000007789 gas Substances 0.000 abstract description 11
- 239000012778 molding material Substances 0.000 abstract description 9
- 238000000465 moulding Methods 0.000 abstract description 5
- 239000000654 additive Substances 0.000 abstract description 4
- 229920000049 Carbon (fiber) Polymers 0.000 abstract description 2
- 239000004917 carbon fiber Substances 0.000 abstract description 2
- 238000005260 corrosion Methods 0.000 abstract description 2
- 230000007797 corrosion Effects 0.000 abstract description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract description 2
- 239000000945 filler Substances 0.000 abstract description 2
- 239000003365 glass fiber Substances 0.000 abstract description 2
- 239000010445 mica Substances 0.000 abstract description 2
- 229910052618 mica group Inorganic materials 0.000 abstract description 2
- 229920000642 polymer Polymers 0.000 abstract description 2
- 239000003381 stabilizer Substances 0.000 abstract description 2
- 239000000454 talc Substances 0.000 abstract description 2
- 229910052623 talc Inorganic materials 0.000 abstract description 2
- 230000002745 absorbent Effects 0.000 abstract 1
- 239000002250 absorbent Substances 0.000 abstract 1
- 230000000994 depressogenic effect Effects 0.000 abstract 1
- 238000002156 mixing Methods 0.000 abstract 1
- 239000012744 reinforcing agent Substances 0.000 abstract 1
- 238000002845 discoloration Methods 0.000 description 9
- 230000000694 effects Effects 0.000 description 7
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 239000011889 copper foil Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000008188 pellet Substances 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000001746 injection moulding Methods 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229920004695 VICTREX™ PEEK Polymers 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- KSEBMYQBYZTDHS-HWKANZROSA-N ferulic acid Chemical group COC1=CC(\C=C\C(O)=O)=CC=C1O KSEBMYQBYZTDHS-HWKANZROSA-N 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
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。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a heat-resistant resin molding material characterized by adding alumina hydrate to a polyethersun resin, and more specifically relates to a molding material. The present invention relates to a polyethersulfone resin composition that can reduce corrosion of molds and the like.
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
形性により成形されて、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°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 can be molded with various moldability and is widely used in mechanical parts, electrical and electronic parts, etc. . However, the processing temperature of polyether sulfone resin is quite high at 340-400℃, and at such high temperatures some metal corrosive gas is generated, which may corrode the mold and molding machine during the molding process. In addition, when a molded product is aged at a temperature of 100° C. or higher, a problem arises in that corrosive gas is 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.
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
へのアル旦す水和物Q添加が有効であることを見出し本
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 conducted various studies and found that the addition of alkaline hydrate Q to polyether sulfone resin was effective, and completed the present invention. did.
すなわち、本発明はポリエーテルスルホン樹脂100重
量部に対してアルミナ水和物0.01〜20重量部を添
加することを特徴とする樹脂m酸物である。That is, the present invention is a resin m-acid characterized in that 0.01 to 20 parts by weight of alumina hydrate is added to 100 parts by weight of polyether sulfone resin.
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、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 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 with three essential bonding units: an arylene bond (aromatic bond), an ether bond, and a sulfone bond. For example, the following structure is a very typical example. Can be mentioned.
(1) −(−o−O−s 02−■−〉−CH)
(2) −(−0−■−502−■−〇−〇−C−0
0−)−CH3
(3) −(−0−■−502−■−〇−00−0−
00−) −CH3
(4) −(−0−O−S(h−■−■−〇 −00
−C−00−’) −Hs
(5) −(−0−■−so、0−o−■−〇−)−
(6) −(−0−O−SCh−O−O−5O2−■
−0−■−)−(7) −(−0−O−S(h−■−
0−■−CH2−■−)−これらのポリエーテルスルホ
ン
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。(1) -(-o-O-s 02-■->-CH) (2) -(-0-■-502-■-〇-〇-C-0
0-)-CH3 (3) -(-0-■-502-■-〇-00-0-
00-) -CH3 (4) -(-0-O-S(h-■-■-〇 -00
-C-00-') -Hs (5) -(-0-■-so, 0-o-■-〇-)-
(6) -(-0-O-SCh-O-O-5O2-■
-0-■-)-(7) -(-0-O-S(h-■-
0-■-CH2-■-)-These polyether sulfones can be easily produced by the methods described in Japanese Patent Publication No. 10067-1980, Japanese Patent Publication No. 7799-1979, and Japanese Patent Publication No. 617-1974.
また本発明で用いられるアル藁す水和物とは一般に[A
Ltoz ・、H,O ]という化学組成の化合物で
あり、例えば(ALzOi ・JzO)、(Atzo
i ・H2O)等があり、さらには水酸化アルミニウ
ム[AL(OHン,コもこれに含まれる。In addition, the alkaline hydrate used in the present invention is generally [A
Ltoz ・, H, O ], for example, (ALzOi ・JzO), (Atzo
i ・H2O), and furthermore, aluminum hydroxide [AL(OHn, ko) is also included.
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 alumina hydrate 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. 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.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 polyether sulfone resin according to the present invention is usually 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. It is preferable to use this molding material in the form of pellets. Next, the pellets are 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、鰭型剤等の各種添加剤を樹脂&[l
酸物の品質を損なわない範囲で混和しても良い。In the present invention, fillers such as talc, mica, and glass beads may be added to the polyether sulfone resin molding material as necessary.
Various additives such as glass fibers, carbon fibers, potassium titanate fibers, aramid fibers, ceramic fibers, stabilizers, ultraviolet absorbers, colorants, fin shaping agents, etc. are added to the resin and [l].
They may be mixed as long as the quality of the acid is not impaired.
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
S3600P (商標、英国インペリアルケミカルイン
ダ。Examples 1 to 4 and Comparative Examples 1 to 3 VICTREX PE as polyether sulfone resin
S3600P (trademark, Imperial Chemical Ind., UK).
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−でトライブレンドした.こ
の混合物を二軸押出機を用いてシリンダー温度320〜
350°Cで押出し、均一なペレット状の成形材料を得
た。Stry Co.) powder and various additives were mixed in the proportions shown in Table 1 and tri-blended using a Henschel mixer. This mixture was processed using a twin-screw extruder at a cylinder temperature of 320~
It was extruded at 350°C to obtain a uniform pellet-shaped molding material.
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MT(lりより判断した.
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、三角フラスコ表1
^r (Oil)3 ・・隼U三イ[1m式1≧ド1
上AZnO=thJ三イと3式m
?LI演1丘ヒ劣ゴ牛 洛■寛・ ・ ・ 320″
C荷重・・・2.16kg
表2
に1Og入れ、中に5X5mmの銅箔を吊して、150
″C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。In addition, the fluidity of each sample was determined based on the melt index (hereinafter referred to as MT) in accordance with JIS K7210.
Furthermore, the cylinder temperature is 33 for the above pellets.
Injection molding was performed at 0 to 360°C. The molded product was crushed, and as shown in Fig. 2, an Erlenmeyer flask was prepared.
Upper AZnO=thJ3i and 3typem? LI performance 1 hill low grade cow Raku ■ ・ ・ 320″
C load...2.16kg Put 10g in Table 2, hang a 5x5mm copper foil inside, and
The copper foil was allowed to stand in a high temperature bath for 100 hours, and 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 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 It was shown more.
〔発明の効果]
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、押出成形時の酸形金形、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&[l放物よ
りえられたペレット状底形材料(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 l:金属
缶 2:金属缶 3:試料4:w4材 を示す。[Effects of the Invention] 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 acid 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 in electrical and electronic parts because the generation of corrosive gases is suppressed. It is a schematic diagram showing a discoloration test of steel materials using a pellet-like bottom-shaped material (sample) obtained from a paraboloid, and each number indicates the following: l: metal can 2: metal can 3: sample 4: W4 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 (2)
アルミナ水和物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。(1) A polyethersulfone resin composition characterized in that 0.01 to 20 parts by weight of alumina hydrate is added to 100 parts by weight of the polyethersulfone resin.
ムであることを特徴とする樹脂組成物。(2) A resin composition, wherein the alumina hydrate according to claim 1 is aluminum hydroxide.
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 true JPH03199263A (en) | 1991-08-30 |
JP2683437B2 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) |
Citations (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
Patent Citations (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 |
Also Published As
Publication number | Publication date |
---|---|
JP2683437B2 (en) | 1997-11-26 |
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