JPH02255861A - Ic socket - Google Patents
Ic socketInfo
- Publication number
- JPH02255861A JPH02255861A JP30939589A JP30939589A JPH02255861A JP H02255861 A JPH02255861 A JP H02255861A JP 30939589 A JP30939589 A JP 30939589A JP 30939589 A JP30939589 A JP 30939589A JP H02255861 A JPH02255861 A JP H02255861A
- Authority
- JP
- Japan
- Prior art keywords
- group
- socket
- polyimide
- aromatic group
- aromatic
- 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
Links
- 229920001721 polyimide Polymers 0.000 claims abstract description 30
- 239000004642 Polyimide Substances 0.000 claims abstract description 29
- 239000000126 substance Substances 0.000 claims abstract description 7
- 125000003118 aryl group Chemical group 0.000 claims abstract description 5
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims abstract description 3
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims abstract description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 claims description 2
- 125000004149 thio group Chemical group *S* 0.000 claims description 2
- 125000003367 polycyclic group Chemical group 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 4
- 239000007858 starting material Substances 0.000 abstract 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 16
- 239000003365 glass fiber Substances 0.000 description 14
- 238000001746 injection moulding Methods 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 238000002347 injection Methods 0.000 description 9
- 239000007924 injection Substances 0.000 description 9
- 239000000843 powder Substances 0.000 description 9
- 239000002994 raw material Substances 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 239000008188 pellet Substances 0.000 description 7
- -1 polybutylene terephthalate Polymers 0.000 description 7
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 6
- 238000005452 bending Methods 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 6
- 239000004697 Polyetherimide Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 229920001601 polyetherimide Polymers 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 125000006158 tetracarboxylic acid group Chemical group 0.000 description 2
- RLLPVAHGXHCWKJ-IEBWSBKVSA-N (3-phenoxyphenyl)methyl (1s,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-IEBWSBKVSA-N 0.000 description 1
- VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 description 1
- MFTFTIALAXXIMU-UHFFFAOYSA-N 3-[4-[2-[4-(3-aminophenoxy)phenyl]-1,1,1,3,3,3-hexafluoropropan-2-yl]phenoxy]aniline Chemical compound NC1=CC=CC(OC=2C=CC(=CC=2)C(C=2C=CC(OC=3C=C(N)C=CC=3)=CC=2)(C(F)(F)F)C(F)(F)F)=C1 MFTFTIALAXXIMU-UHFFFAOYSA-N 0.000 description 1
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical group OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 1
- 101100348017 Drosophila melanogaster Nazo gene Proteins 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- BBRLKRNNIMVXOD-UHFFFAOYSA-N bis[4-(3-aminophenoxy)phenyl]methanone Chemical compound NC1=CC=CC(OC=2C=CC(=CC=2)C(=O)C=2C=CC(OC=3C=C(N)C=CC=3)=CC=2)=C1 BBRLKRNNIMVXOD-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229940090668 parachlorophenol Drugs 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920006259 thermoplastic polyimide Polymers 0.000 description 1
Landscapes
- Connecting Device With Holders (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、特定のポリイミドを原料とする集積回路(以
下ICと略称)用のゾケッ1〜に関し7、特にバーンイ
ン (burn−in)用ICソケットに関するもので
あるゆ
[従来の技術]
一般にICは、その信頼性を確認する為に機器への装着
に先立って高温下での性能チエツク、いわゆるバーン・
インが実施される、
バーンインは、はぼ動作状態に通電したICを通常は7
0−170°Cの高温状態に保つで動作状態の劣化或い
は不安定状態の有無宿のチエツクを行うものである。こ
のテストに合格したICは各種の機器に対してモ分な信
頼性を保障引ることになる。Detailed Description of the Invention [Field of Industrial Application] The present invention relates to semiconductors 1 to 7 for integrated circuits (hereinafter abbreviated as IC) made from a specific polyimide, and particularly to burn-in ICs. Related to sockets [Prior art] In general, ICs undergo a performance check under high temperature, a so-called burn test, before being installed in equipment to confirm their reliability.
A burn-in is performed to bring the energized IC into an operating state, usually at 7
The device is kept at a high temperature of 0-170°C to check for deterioration in operating conditions or instability. ICs that pass this test will be highly reliable for various types of equipment.
ところで、ICをプリント基板に結合するニコネクショ
ン部であるICソケットは、I Cを挿入した状態で上
記の高温状態に曝露される為、それに使用される槍縁材
料には当然耐熱性が要求される。By the way, the IC socket, which is the connection part that connects the IC to the printed circuit board, is exposed to the above-mentioned high temperature conditions with the IC inserted, so the lance material used for it is naturally required to have heat resistance. Ru.
しかしながら、ICの性能テスト(バーンイン)は評価
の促進および信頼性の向上を目的として近年益々高温下
で実施される様になり、従来の樹脂で製造されたICソ
ケットではとうてい対応できないケースも出てくる様に
なった。However, in recent years, IC performance tests (burn-in) have been conducted at increasingly high temperatures for the purpose of promoting evaluation and improving reliability, and there are cases where IC sockets made of conventional resin cannot handle the test. It looked like it was coming.
例えば、ガラス繊維強化のポリブチレンテレフタレート
樹脂、ポリブチレンテレフタレート樹脂、ナイロン樹脂
等は120℃前後までは使用可能であるが、それ以上に
なると寸法安定性、クリープ特性等の低下が著しくなる
為に使用に耐えない。従って、更に耐熱性の良好なポリ
フェニレンサルファイド樹脂、ポリサルホン樹脂、ポリ
エーテルサルホン樹脂等が使用される様になってきた。For example, glass fiber-reinforced polybutylene terephthalate resin, polybutylene terephthalate resin, nylon resin, etc. can be used up to around 120℃, but if the temperature exceeds that temperature, dimensional stability, creep properties, etc. will deteriorate significantly, so they cannot be used. I can't stand it. Therefore, polyphenylene sulfide resin, polysulfone resin, polyether sulfone resin, etc., which have better heat resistance, have come to be used.
しかしながら、いずれの樹脂も実際の使用温度は170
℃前後までに止まっている。However, the actual operating temperature for both resins is 170°C.
It stopped at around ℃.
また、単に耐熱性だけでなく洗浄時の耐薬品性(例えば
イソプロピルアルコール、エチルアルコール、トルエン
、ベンゼン、トリクレン、クロロセン、フレオン、アセ
トン、メタノール等に対して)、耐水蒸気性、難燃性等
に関しても優れた特性を要求されるケースが多く、従来
の樹脂で対応するには困難があった。In addition to heat resistance, we also provide chemical resistance during cleaning (e.g. against isopropyl alcohol, ethyl alcohol, toluene, benzene, trichlene, chlorocene, freon, acetone, methanol, etc.), water vapor resistance, flame retardance, etc. In many cases, excellent properties are required, making it difficult for conventional resins to meet these demands.
さらに耐熱性、耐薬品性等に優れた樹脂としてポリイミ
ドが良く知られているが、従来のポリイミドはポリイミ
ドの状態では溶融流動することがない為−船釣な成型方
法、例えば射出成型により成型体を製造することは不可
能であった。またポリイミドの技術範囲に入るが、例夕
1的にエーテル結合を分子内に有するテトラカルボン酸
二無水物を原料とするポリエーテルイミド(米国ゼネラ
ルエレクトリック社製、商標、ULTEMlooO等)
は高温時、溶融流動する為、圧縮成型、射出成型等によ
り成型体を製造することは可能である。しかしこのポリ
エーテルイミドをICソケットに適用した場合でも、耐
熱性、耐薬品性において満足しつる状態にはなかった。Furthermore, polyimide is well known as a resin with excellent heat resistance, chemical resistance, etc., but since conventional polyimide does not melt and flow in its polyimide state, it can be molded using conventional molding methods, such as injection molding. It was impossible to manufacture. Also within the technical scope of polyimide, for example, polyetherimide made from tetracarboxylic dianhydride having an ether bond in the molecule (manufactured by General Electric Company, USA, trademark, ULTEMlooO, etc.)
Because it melts and flows at high temperatures, it is possible to manufacture molded bodies by compression molding, injection molding, etc. However, even when this polyetherimide was applied to IC sockets, the heat resistance and chemical resistance were not satisfactory.
[発明が解決しようとする課題]
本発明の目的は、特定のポリイミドを原料として、耐熱
性、耐薬品性、耐水蒸気性、難燃性等に優れたICソケ
ットを提供することにある。[Problems to be Solved by the Invention] An object of the present invention is to provide an IC socket that uses a specific polyimide as a raw material and has excellent heat resistance, chemical resistance, water vapor resistance, flame retardance, etc.
[課題を解決するための手段]
本発明考らは、上記のICソケツI・用素材に関して種
々検討を重ねた結果、特定のポリイミドを用いることに
より、上述のような従来品の欠点が解消され、著しく優
れた性能を有するICソケットが得られることを見出し
、本発明を完成した。[Means for Solving the Problems] As a result of various studies regarding the materials for the above-mentioned IC socket I, the present invention has been made to solve the above-mentioned drawbacks of conventional products by using a specific polyimide. They discovered that an IC socket with significantly superior performance could be obtained, and completed the present invention.
即ち、本発明によるICソケットは、下記の式(I)の
繰り返し単位を有するポリイミドからなるものである。That is, the IC socket according to the present invention is made of polyimide having a repeating unit of the following formula (I).
族基、単環式芳香族基、縮合多環式芳香族基、および芳
香族基が直接または架橋員により相互に連結された非縮
合多環式芳香族基からなる群より選ばれた4価の基を表
わす。)
上記ポリイミドは、下記の式(II)に示すエーテルジ
アミンと、
(式中、Xは前に同じ)
下記式 (III)に示すテトラカルボン酸二無水物一
種以上とを反応させて得られるポリイミドである。A tetravalent group selected from the group consisting of a group group, a monocyclic aromatic group, a fused polycyclic aromatic group, and a non-fused polycyclic aromatic group in which aromatic groups are interconnected directly or through a bridge member. represents the group of ) The above polyimide is a polyimide obtained by reacting an ether diamine represented by the following formula (II) with one or more tetracarboxylic dianhydrides represented by the following formula (III) (wherein X is the same as before). It is.
(I)
(式中、Xは直結、炭素数1〜10の二価の炭化水素基
、六フッ素化されたイソプロピリデン基、カルボニル基
、チオ基、またはスルホニル基であり、またRは炭素数
2以上の脂肪族基、環式脂肪(式中、Rは前に同じ)
本発明に係るポリイミドはエーテル結合を有するジアミ
ンを原料として用いることに特徴がある。具体的には例
えば特開昭61−143478 、同62−68817
、同62−86021、米国特許第48.473.49
5号等に記載の方法により容易に製造でき、これらの方
法により製造された熱可塑性ポリイミドの全てが本発明
に使用できる。中でも好ましいポリイミドは、下記の原
料を用いて製造できる。即ち、エーテルジアミンとして
4.4°−ビス[4−(3−アミノフェノキシ)フェニ
ル]スルフィド、4.4゛−ビス[4−(3−アミノフ
ェノキシ)フェニル]スルホン、4,4゛−ビス(3−
アミノフェノキシ)ベンゾフェノン、4,4°−ビス(
3−アミノフェノキシ)ビフェニル、 2.2−ビス[
4−(3−アミノフェノキシ)フェニルコプロパンまた
は2.2−ビス[4−(3−アミノフェノキシ)フェニ
ル]−1、1,1,3,3,3−ヘキサフルオロプロパ
ンであり、これらの中から選ばれる化合物を単独、また
は2種以上を混合したもの、またテトラカルボン酸二無
水物として、ピロメリット酸二無水物、 3.3’。(I) (wherein, X is a direct bond, a divalent hydrocarbon group having 1 to 10 carbon atoms, a hexafluorinated isopropylidene group, a carbonyl group, a thio group, or a sulfonyl group; Two or more aliphatic groups, cycloaliphatic (in the formula, R is the same as before) The polyimide according to the present invention is characterized in that a diamine having an ether bond is used as a raw material.Specifically, for example, JP-A No. 61 -143478, 62-68817
, No. 62-86021, U.S. Patent No. 48.473.49
It can be easily produced by the method described in No. 5 etc., and all thermoplastic polyimides produced by these methods can be used in the present invention. Among them, preferred polyimides can be produced using the following raw materials. That is, 4.4°-bis[4-(3-aminophenoxy)phenyl]sulfide, 4.4′-bis[4-(3-aminophenoxy)phenyl]sulfone, 4,4′-bis( 3-
aminophenoxy)benzophenone, 4,4°-bis(
3-aminophenoxy)biphenyl, 2.2-bis[
4-(3-aminophenoxy)phenylcopropane or 2,2-bis[4-(3-aminophenoxy)phenyl]-1,1,1,3,3,3-hexafluoropropane, among which A compound selected from the following may be used alone or as a mixture of two or more thereof, and as a tetracarboxylic dianhydride, pyromellitic dianhydride, 3.3'.
4.4゛−ビフェニルテトラカルボン酸二無水物、3゜
3’、 4.4’ −ベンゾフェノンテトラカルボン酸
二無水物、 3.3°、4.4’−ジフェニルテトラカ
ルボン酸二無水物、p−フェニ1./ンオギシジ(4−
フタル酸)二無水物であり、これらの中から選ばれる化
合物を単独、または2f!1以上を混合したものである
。4.4゛-Biphenyltetracarboxylic dianhydride, 3゜3', 4.4'-benzophenonetetracarboxylic dianhydride, 3.3°, 4.4'-diphenyltetracarboxylic dianhydride, p -Feni 1. / Nwogishiji (4-
phthalic acid) dianhydride, and a compound selected from these can be used alone or 2f! It is a mixture of one or more.
上記により得られる本発明のポリイミドの対数粘度は、
通常0.35〜0.65 d12/g、好ましくは04
40〜0.60 df2.7g の範囲のものである
。この対数粘度が上記の範囲を越えて0.35以下であ
ると機械特性、耐久性が不十分となり、また0、60以
上であると成型性が悪化し射出成型困難どなる。この対
数粘度はパラクロロフェノール/フェノール(90/1
0重量比)の混合溶媒中、濃度0.5g/100mβ−
溶媒で加熱溶解した後、35℃に冷却して測定される。The logarithmic viscosity of the polyimide of the present invention obtained as above is:
Usually 0.35-0.65 d12/g, preferably 04
It is in the range of 40 to 0.60 df2.7g. If the logarithmic viscosity exceeds the above range and is less than 0.35, the mechanical properties and durability will be insufficient, and if it is more than 0.60, moldability will deteriorate and injection molding will become difficult. This logarithmic viscosity is parachlorophenol/phenol (90/1
0 weight ratio) in a mixed solvent with a concentration of 0.5 g/100 mβ-
After heating and dissolving with a solvent, it is cooled to 35°C and measured.
上記ポリイミドを原料としてICソケットを製造しつる
が、この場合耐熱性、機械特性等を更に付与する目的で
このポリイミドにガラス繊維を併用してもよい。Although IC sockets are manufactured using the above-mentioned polyimide as a raw material, in this case, glass fiber may be used in combination with this polyimide for the purpose of further imparting heat resistance, mechanical properties, etc.
併用しつるガラス繊維はアルカリ(NazO)含有量、
繊維長および径により各種のものが市販されているが、
これらはいずれでも用いることができ、特に限定される
ものではない。その使用量はポリイミドとガラス繊維を
含む組成物に対してガラス繊維が40重量%以下、好ま
しくは30重量%以下である。40重量%以上のガラス
m維を使用すると組成物の溶融流動性が悪くなり、射出
成形性が悪くなり、さらには成形物の表面状態も悪くな
る。ガラス繊維の他に、顔料、ガラス繊t、i以外の各
種充填剤、増量剤、安定剤、滑剤等を添加することも可
能である。The glass fiber used in combination has alkali (NazO) content,
Various types are commercially available depending on fiber length and diameter, but
Any of these can be used and is not particularly limited. The amount of glass fiber used is 40% by weight or less, preferably 30% by weight or less, based on the composition containing polyimide and glass fiber. If 40% by weight or more of glass m fibers is used, the melt flowability of the composition will be poor, injection moldability will be poor, and the surface condition of the molded product will also be poor. In addition to glass fibers, it is also possible to add pigments, various fillers other than glass fibers t and i, extenders, stabilizers, lubricants, etc.
本発明のICソケットは原料としてのポリイミドを粉状
またはベレット状態で、さらにはポリイミドとガラス繊
維あるいは各種添加剤を併用する場合には、予め、熱ロ
ール、バンバリーミキサ−、ヘンシェルミキサー、ブラ
ベンダー、タンブラ−2押出機などの通常のブレンド装
置を利用し、溶融または混線したのち粉状またはペレッ
ト状態で、射出成型により成型できる。The IC socket of the present invention uses polyimide as a raw material in powder or pellet form, and when polyimide and glass fiber or various additives are used together, it is prepared in advance using a hot roll, Banbury mixer, Henschel mixer, Brabender, etc. It can be melted or mixed using a conventional blending device such as a tumbler 2 extruder, and then molded into powder or pellets by injection molding.
射出成型条件は、−船釣にはシリンダー温度300〜4
50℃、金型温度150〜230℃、射出圧力500〜
1500にg/cm”の範囲で、各種のICソケット;
例λばクワッドフラットパッケージ(QuardFla
t Package:QFP)代表的にはビン数40〜
100、ピッチ0.5mmのもの、リードレスチップキ
ャリア(Leadless (:hip Carroe
r:LCC)代表的にはビン数18〜84、ピッチ1.
27mmのもの、デュアルインラインパッケージ(Du
al In Line Package:DIP)、シ
ングルインラインパッケージ(Single In L
inePackage:SIP ) 、スモールアウト
ラインパッケージ(Small Out Line P
ackage:5OP) 、チッとキャリアー(Chi
p Carrier:CC) 、 ピングクツドア1/
イ・サブストiノート(Pin Grid Array
5ubstrate:PGA)等各種のICソケット
が製造できる。Injection molding conditions are - Cylinder temperature 300 to 4 for boat fishing
50℃, mold temperature 150~230℃, injection pressure 500~
Various IC sockets in the range of 1500 to 1500 g/cm;
For example, quad flat package (QuardFla)
t Package: QFP) Typically, the number of bins is 40 or more.
100, pitch 0.5mm, leadless chip carrier (:hip Carroe
r: LCC) Typically, the number of bins is 18 to 84, and the pitch is 1.
27mm one, dual inline package (Du
al In Line Package: DIP), Single In Line Package (Single In L
inePackage:SIP), Small Outline Package (Small Out Line P)
ackage: 5OP), Chito Carrier (Chi
p Carrier: CC), Ping Kuts Door 1/
i Subst i Note (Pin Grid Array
Various types of IC sockets such as 5-substrate (PGA) can be manufactured.
[実施例] 以下、本発明を実施例によって説明する。[Example] Hereinafter, the present invention will be explained by examples.
実施例1
成分 (IIとしてのどロメリット酸二無水物と成分(
II)としての4,4−ビス(3−アミノフェノキシ)
ビフェニルを原料として得られた対数粘度0゜45 d
β/g のポリイミド粉を押出機によりシリンダー温度
400 ’Cにてべ+、/ット状に押出した。Example 1 Ingredients (thromellitic dianhydride as II and ingredients (
4,4-bis(3-aminophenoxy) as II)
Logarithmic viscosity obtained from biphenyl as raw material: 0°45 d
A polyimide powder of β/g was extruded into the shape of a sheet using an extruder at a cylinder temperature of 400'C.
ここで対数粘度はパラクロロフ、−Lノール/°ノエノ
ール(重量比90/10)の混合溶媒中、濃度0.5g
/loom f2−溶媒で加熱溶解した後、35°Cに
冷却し測定した値である。Here, the logarithmic viscosity is parachloroph, in a mixed solvent of -Lnol/°noenol (weight ratio 90/10), concentration 0.5g
/room f2- This is a value measured after heating and dissolving in a solvent and then cooling to 35°C.
このべ1ノツト・をシリンダー温度380−410 ’
C1金型温度190℃、射出圧カフ00にgf/cm2
の条件F)こ射出成形し゛て、ビン数6・1、ピッチ0
.5mmのICソケット(クワッドフラットパッケージ
: QFP)を得た。このものは茶褐色・透明Cシルバ
ー、ヒケ、フローマーク等のない優れたものであった。Note: The cylinder temperature is 380-410'
C1 mold temperature 190℃, injection pressure cuff 00gf/cm2
Condition F) This injection molding has a number of bins of 6.1 and a pitch of 0.
.. A 5 mm IC socket (quad flat package: QFP) was obtained. This product was brownish-brown, transparent C-silver, and had no sink marks, flow marks, etc., and was excellent.
この■Cソケッ1−を用いて次の試験を行った。The following test was conducted using this ■C socket 1-.
■トルエ゛ノおよびトリクレンに10日間浸漬後の外観
、■2 kg/cm2の加熱水蒸気中に200時間曝露
後の外観、0230℃の加熱オーブン中に100時間曝
露後の外観、いずれの試験においても外観」二の変化は
なかった。■Appearance after 10 days of immersion in tolueno and trichlene; ■Appearance after 200 hours of exposure to heated steam at 2 kg/cm2; Appearance after 100 hours of exposure to 0230°C heated oven. There was no change in appearance.
尚、本べ!ノットより同一成形条件下にASTMに規定
する試験片を作成して物性を測定しまたところ、熱変形
温度240℃(D−6411)、曲げ強度1400kg
/cm2(D−790)、限界酸素指数47 (3,2
mm l’J−1D2863)を示した。Also, book! A test piece specified by ASTM was prepared from the knot under the same molding conditions and its physical properties were measured.The heat distortion temperature was 240℃ (D-6411) and the bending strength was 1400kg.
/cm2 (D-790), limiting oxygen index 47 (3,2
mm l'J-1D2863).
従って、このものがICソケットとして良好な性質を有
していることが判る。Therefore, it can be seen that this product has good properties as an IC socket.
比較例1
実施例1に於けるポリイミド粉の代りにポリエーテルイ
ミド IJLTEMlooO(商標、米国ゼネラルエレ
クトリック社製)のベレッ1〜をシリンダー温度330
〜400℃、金型温度150℃、射出圧力800Kgf
/cm2の条件下に射出成形して、実施例1ど同様のN
Cソケット(クワッドフラットバッケー″:/:QFP
)を得た。Comparative Example 1 Instead of the polyimide powder in Example 1, polyetherimide IJLTEMlooO (trademark, manufactured by General Electric Company, USA) was used at a cylinder temperature of 330.
~400℃, mold temperature 150℃, injection pressure 800Kgf
/cm2 by injection molding under the same conditions as in Example 1.
C socket (quad flat backer”:/:QFP
) was obtained.
このICソケットをトリク1ノンに10日間浸漬したど
ころ、全面にわたり著しく白化した。また2 kg/c
m2の加熱水蒸気中に200時間曝露後、ICソケット
には多数のクラックが発生していた。さらに230℃の
加熱オーブン中に100時間曝露後、ICソケットの形
状が原形を止めえない稈に著しく変形した。When this IC socket was immersed in Triku 1 Non for 10 days, the entire surface became noticeably whitened. Also 2 kg/c
After being exposed to m2 of heated steam for 200 hours, the IC socket had many cracks. Furthermore, after being exposed to a heating oven at 230° C. for 100 hours, the shape of the IC socket was significantly deformed into a culm that could not be kept in its original shape.
実施例2
実施例1で用いたポリイミド粉70重量部にガラス繊維
(3mm長、アスペクト比250) 30重量部をタン
ブラ−により充分攪拌した後、べlノット化した。Example 2 70 parts by weight of the polyimide powder used in Example 1 and 30 parts by weight of glass fibers (3 mm length, aspect ratio 250) were sufficiently stirred in a tumbler and then formed into bell knots.
次いで、射出成形機ζこよりシリンダー温度390〜4
20℃、金型温度200°C1射出圧力1000にgf
/cm2の条件下に実施例1と同様のICソケット・を
成形したところ、シルバー、ヒケ、フローマーク等の無
い優れたものが得られた。Next, the cylinder temperature from the injection molding machine ζ is 390~4
20℃, mold temperature 200℃1 injection pressure 1000gf
When an IC socket similar to that of Example 1 was molded under the condition of /cm2, an excellent product was obtained without silver, sink marks, flow marks, etc.
このICソケットを用いて実施例1と同様にトルエンお
よびトリクレンに10日間浸漬後の外観、2 kg/c
m2の加熱水蒸気中に200時間曝露後の外観、いずれ
の試験においても外観上の変化はなかった。Appearance after immersing this IC socket in toluene and trichlene for 10 days in the same manner as in Example 1, 2 kg/c
There was no change in appearance after 200 hours of exposure to m2 of heated steam in any of the tests.
尚、本ベレッ]−より同一成形条件下にASTMに規定
する試験片を作成して物性を測定し7たところ、熱変形
温度243℃、曲げ強度2400kg/cm”であった
。A test piece specified by ASTM was prepared under the same molding conditions under the same molding conditions and the physical properties were measured, and it was found that the heat distortion temperature was 243°C and the bending strength was 2400 kg/cm''.
比較例2
実施例2に於けるガラス繊維入りポリイミドベレットの
代りにガラス繊維30%含有のポリエーテルイミドl]
LTEM2300 (商標、米国ゼネラルエ1ツクトリ
ック社製)のベレットをシリンダ・−温度340〜41
0℃、金型温度150℃、射出圧力100100O/c
m”の条件下に射出成形して、実施例1と同様のICソ
ケット(クワッドフラットパッケージQFP)を得た。Comparative Example 2 Polyetherimide containing 30% glass fiber instead of the glass fiber-containing polyimide pellet in Example 2]
LTEM2300 (trademark, manufactured by General Electric Company, USA) pellet was heated to a cylinder temperature of 340 to 41.
0℃, mold temperature 150℃, injection pressure 100100O/c
An IC socket (quad flat package QFP) similar to that in Example 1 was obtained by injection molding under the conditions of ``m''.
このICソケットをトリクレンに10日間浸漬したとこ
ろ、全面にわたり著しく白化し、ガラス繊維の浮き出し
が認められた。また2 kg/cm2の加熱水蒸気中に
200時間曝露後も同様に全面が自作した。さらに23
0℃の加熱オーブン中に100時17F曝露後、ICソ
ケットの形状が崩れ、ピッチのぐらつきが目立つ様にな
った。When this IC socket was immersed in Triclean for 10 days, the entire surface was significantly whitened and glass fibers were observed to be embossed. The entire surface was also self-made after being exposed to heated steam at 2 kg/cm2 for 200 hours. 23 more
After being exposed to a heating oven at 0°C at 17F for 100 hours, the shape of the IC socket collapsed and pitch wobble became noticeable.
実施例3
実施例2で用いたベレッ1へを原料として、シリンダー
温度390〜420℃、金型温度200℃、射出圧力9
00にgf/cm2の条件により、ビン数84、ピッチ
1.27mmのICソケット (リードレスチップキャ
リア; LCC)を成形したところ、シルバー ピケ、
フローマーク等の無い優れたものが得られた。Example 3 Using the beret 1 used in Example 2 as a raw material, the cylinder temperature was 390 to 420°C, the mold temperature was 200°C, and the injection pressure was 9.
When an IC socket (leadless chip carrier; LCC) with 84 bins and a pitch of 1.27 mm was molded using gf/cm2 conditions on 00, silver picket,
An excellent product with no flow marks etc. was obtained.
このICソケットを用いて実施例1と同様にトルエンお
よびl・リクレンに10日間浸漬後の外観、2 kg/
am2の加熱水蒸気中に200時間曝露後の外観、いず
れの試験においても外観上の変化はなかった。Appearance after immersing this IC socket in toluene and l-licen for 10 days in the same manner as in Example 1, 2 kg/
There was no change in appearance after 200 hours of exposure to am2 heated steam in any of the tests.
比較例3
比較例2で用いたLILTEM2300のベレットをシ
リンダー温度340〜410℃、金型温度150℃、射
出圧力100100O/cm”の条件下に射出成形して
、実施例3と同様のICソケット(リードレスチップキ
ャリア、 LCC)を得た。Comparative Example 3 The pellet of LILTEM2300 used in Comparative Example 2 was injection molded under the conditions of a cylinder temperature of 340 to 410°C, a mold temperature of 150°C, and an injection pressure of 100,100 O/cm'' to make an IC socket similar to that of Example 3 ( A leadless chip carrier (LCC) was obtained.
このICソケットをトリクレンにIO日間浸漬したとこ
ろ、全面が白化し、ガラス繊維の浮き出しが認められた
。また2 kg/am”の加熱水蒸気中に200時間曝
露後も同様に全面が白化した。更に230℃の加熱オー
ブン中に100時間曝露後、ICソケットの形状が崩れ
、ピッチのぐらつきが目立つ様になった。When this IC socket was immersed in Triclean for 10 days, the entire surface turned white and glass fibers were observed to be embossed. Similarly, after 200 hours of exposure to 2 kg/am'' heated steam, the entire surface turned white.Furthermore, after 100 hours of exposure to 230°C heating oven, the shape of the IC socket collapsed and the pitch wobble became noticeable. became.
実施例4
成分(IN)としてのビス(4−(3−アミノフェノキ
シ)フェニル〕スルフィドと成分(III)としてのピ
ロメリット酸二無水物を原料として得られたポリイミド
粉(対数粘度0.461/g)を実施例1と同様にし2
てべL/ジット化後射出成形機によりビン数64、ピッ
チ0.5mmのICソケット(クワッドフラットパッケ
ージ:QFP)を成形したところ、実施例1ど同様に優
れたものが得られた。Example 4 Polyimide powder (logarithmic viscosity 0.461/ g) as in Example 1 and 2
After forming the L/JIT, an IC socket (quad flat package: QFP) with 64 bottles and a pitch of 0.5 mm was molded using an injection molding machine, and as in Example 1, an excellent product was obtained.
また、実施例1と同様に試験片を作成して物性を測定し
たところ、熱変形温度238℃、曲げ強度1350kg
/cm2であった。In addition, when a test piece was prepared in the same manner as in Example 1 and its physical properties were measured, the thermal deformation temperature was 238°C, and the bending strength was 1350 kg.
/cm2.
実施例5
実施例4で用いたポリ1′ミド粉70重量部に、ガラス
繊維(3mm長、アスペクト比250) 30重量部を
タンブラ−により充分攪拌した後、べLノット化した。Example 5 70 parts by weight of the poly1'amide powder used in Example 4 was thoroughly stirred with 30 parts by weight of glass fibers (3 mm length, aspect ratio 250) in a tumbler, and then formed into L-knots.
次いで、実施例2と同様にしてビン数64、ピッチ0.
5mmのICソケット−(クワッドフラットパッケージ
:QFP)を成形したところ実施例2ど同様に優れたも
のが得られた。Next, in the same manner as in Example 2, the number of bins is 64 and the pitch is 0.
When a 5 mm IC socket (quad flat package: QFP) was molded, an excellent product similar to Example 2 was obtained.
このICソケットを用いて実施例1と同様にトルエンお
よびトリクレンに10日間浸漬後の外観、2 kg/c
m”の加熱水蒸気中に200時間曝露後の外観、230
℃の加熱オーブン中に10/)時間曝露後の外観、いず
れの試験においても外観上の変化はなかった。Appearance after immersing this IC socket in toluene and trichlene for 10 days in the same manner as in Example 1, 2 kg/c
Appearance after 200 hours of exposure to heated steam of 230 m”
There was no change in appearance in any of the tests after exposure for 10/2 hours in a heating oven at .degree.
また、実施例2と同様に試験片を作成して物性を測定し
たところ、熱変形温度242℃、曲げ強度2300kg
/cm2であった。In addition, when a test piece was prepared in the same manner as in Example 2 and its physical properties were measured, the thermal deformation temperature was 242°C, and the bending strength was 2300 kg.
/cm2.
実施例6
成分 (II)としての2.2−ビス(4−(3−アミ
ノフェノキシ)フェニル〕プロパンと成分(III)
としての3.3°、4.4°−ベンゾフェノンテトラカ
ルボン酸二無水物を原料として得られたポリイミド粉(
対数粘度0.45dβ/g)を実施例1と同様にしてベ
レット化後、射出成形機によりビン数64、ピッチ0.
5mmのICソケット(クワッドフラットパッケージ;
QFP)を成形したところ、実施例1と同様に優れた
ものが得られた。Example 6 2.2-bis(4-(3-aminophenoxy)phenyl)propane as component (II) and component (III)
Polyimide powder obtained using 3.3°, 4.4°-benzophenone tetracarboxylic dianhydride as a raw material (
After forming pellets with logarithmic viscosity of 0.45 dβ/g in the same manner as in Example 1, the number of bottles was 64 and the pitch was 0.
5mm IC socket (quad flat package;
QFP) was molded, and as in Example 1, an excellent product was obtained.
また、実施例1と同様に試験片を作成して物性を測定し
たところ、熱変形温度240℃、曲げ強度1370kg
/am”であった。In addition, when a test piece was prepared in the same manner as in Example 1 and its physical properties were measured, the heat distortion temperature was 240°C, and the bending strength was 1370 kg.
/am”.
実施例7
実施例5で用いたポリイミド粉70重量部に、ガラス繊
維(3mm長、アスペクト比250) 30.i置部を
タンブラ−により充分攪拌した後、ベレット化した。Example 7 Glass fiber (3 mm length, aspect ratio 250) was added to 70 parts by weight of the polyimide powder used in Example 5. After thoroughly stirring the i-placed portion with a tumbler, it was formed into pellets.
次いで、実施例2と同様にしてビン数64、ピッチ0.
5mmのICソケット(クワッドフラットパッケージ:
QFP)を成形したところ、実施例2と同様に優れたも
のが得られた。Next, in the same manner as in Example 2, the number of bins is 64 and the pitch is 0.
5mm IC socket (quad flat package:
QFP) was molded, and as in Example 2, an excellent product was obtained.
このICソケットを用いて実施例1と同様にトルエンお
よびトリクレンに10日間浸漬後の外観、2 kg/c
m”の加熱水蒸気中に200時間曝露後の外観、230
℃の加熱オーブン中に100時間曝露後の外観、いずれ
の試験においても外観上の変化はなかった。Appearance after immersing this IC socket in toluene and trichlene for 10 days in the same manner as in Example 1, 2 kg/c
Appearance after 200 hours of exposure to heated steam of 230 m”
There was no change in appearance after 100 hours of exposure in a heating oven at 0.degree. C. in any of the tests.
また、実施例2と同様に試験片を作成して物性を測定し
たところ、熱変形温度241℃、曲げ強度2300kg
/am2であった。In addition, when a test piece was prepared in the same manner as in Example 2 and its physical properties were measured, the thermal deformation temperature was 241°C, and the bending strength was 2300 kg.
/am2.
[発明の効果]
本発明のICソケットは耐熱性、耐薬品性、耐水蒸気性
、難燃性等に優れた新規なポリイミド樹脂を使用してい
る為に、ICソケットとして非常に良好な特性を示すも
のであり、ICの広範なコネクション部分に用い得る。[Effects of the Invention] Since the IC socket of the present invention uses a new polyimide resin that has excellent heat resistance, chemical resistance, water vapor resistance, flame retardancy, etc., it has very good characteristics as an IC socket. It can be used for a wide range of connection parts of ICs.
特許出願人 三井東圧化学株式会社Patent applicant: Mitsui Toatsu Chemical Co., Ltd.
Claims (1)
らなるICソケット ▲数式、化学式、表等があります▼ ( I ) (式中、Xは直結、炭素数1〜10の二価の炭化水素基
、六フッ素化されたイソプロピリデン基、カルボニル基
、チオ基、またはスルホニル基であり、またRは炭素数
2以上の脂肪族基、環式脂肪族基、単環式芳香族基、縮
合多環式芳香族基、および芳香族基が直接または架橋員
により相互に連結された非縮合多環式芳香族基からなる
群より選ばれた4価の基を表わす。)(1) IC socket made of polyimide having the repeating unit of formula (I) ▲ Numerical formulas, chemical formulas, tables, etc. are available ▼ (I) (wherein, X is a direct bond, a divalent hydrocarbon group having 1 to 10 carbon atoms) , a hexafluorinated isopropylidene group, a carbonyl group, a thio group, or a sulfonyl group, and R is an aliphatic group having 2 or more carbon atoms, a cycloaliphatic group, a monocyclic aromatic group, or a fused polycyclic group. (represents a tetravalent group selected from the group consisting of an aromatic group of the formula aromatic group, and a non-fused polycyclic aromatic group in which aromatic groups are interconnected directly or through a bridge member).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30939589A JPH02255861A (en) | 1988-12-27 | 1989-11-30 | Ic socket |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32763688 | 1988-12-27 | ||
JP63-327636 | 1988-12-27 | ||
JP30939589A JPH02255861A (en) | 1988-12-27 | 1989-11-30 | Ic socket |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02255861A true JPH02255861A (en) | 1990-10-16 |
Family
ID=26565940
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30939589A Pending JPH02255861A (en) | 1988-12-27 | 1989-11-30 | Ic socket |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02255861A (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6248782A (en) * | 1985-08-27 | 1987-03-03 | Mitsui Toatsu Chem Inc | Heat-resistant adhesive |
JPS6268817A (en) * | 1985-09-19 | 1987-03-28 | Mitsui Toatsu Chem Inc | Polymide and heat-resistant adhesive consisting of polyimide |
JPS6286021A (en) * | 1985-10-11 | 1987-04-20 | Mitsui Toatsu Chem Inc | Polyimide and heat-resistant adhesive comprising same |
JPS62197426A (en) * | 1986-02-25 | 1987-09-01 | Mitsui Toatsu Chem Inc | Heat-resistant adhesive |
JPS62236858A (en) * | 1986-04-09 | 1987-10-16 | Mitsui Toatsu Chem Inc | Polyimide resin composition |
-
1989
- 1989-11-30 JP JP30939589A patent/JPH02255861A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6248782A (en) * | 1985-08-27 | 1987-03-03 | Mitsui Toatsu Chem Inc | Heat-resistant adhesive |
JPS6268817A (en) * | 1985-09-19 | 1987-03-28 | Mitsui Toatsu Chem Inc | Polymide and heat-resistant adhesive consisting of polyimide |
JPS6286021A (en) * | 1985-10-11 | 1987-04-20 | Mitsui Toatsu Chem Inc | Polyimide and heat-resistant adhesive comprising same |
JPS62197426A (en) * | 1986-02-25 | 1987-09-01 | Mitsui Toatsu Chem Inc | Heat-resistant adhesive |
JPS62236858A (en) * | 1986-04-09 | 1987-10-16 | Mitsui Toatsu Chem Inc | Polyimide resin composition |
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