JPH11323131A - Thermoplastic resin composition and heat-resistant tray for ic - Google Patents
Thermoplastic resin composition and heat-resistant tray for icInfo
- Publication number
- JPH11323131A JPH11323131A JP10127293A JP12729398A JPH11323131A JP H11323131 A JPH11323131 A JP H11323131A JP 10127293 A JP10127293 A JP 10127293A JP 12729398 A JP12729398 A JP 12729398A JP H11323131 A JPH11323131 A JP H11323131A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- thermoplastic resin
- resin composition
- weight
- 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
- 239000011342 resin composition Substances 0.000 title claims abstract description 29
- 229920005992 thermoplastic resin Polymers 0.000 title claims abstract description 28
- 125000003118 aryl group Chemical group 0.000 claims abstract description 56
- 229920005989 resin Polymers 0.000 claims abstract description 47
- 239000011347 resin Substances 0.000 claims abstract description 47
- 229920005668 polycarbonate resin Polymers 0.000 claims abstract description 29
- 239000004431 polycarbonate resin Substances 0.000 claims abstract description 29
- 229920002492 poly(sulfone) Polymers 0.000 claims abstract description 25
- 229920000049 Carbon (fiber) Polymers 0.000 claims abstract description 8
- 239000004917 carbon fiber Substances 0.000 claims abstract description 8
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims abstract description 8
- 238000000465 moulding Methods 0.000 claims abstract description 6
- 239000000155 melt Substances 0.000 claims description 14
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 9
- 239000002994 raw material Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 6
- 239000000203 mixture Substances 0.000 description 17
- 239000000835 fiber Substances 0.000 description 6
- 238000001746 injection moulding Methods 0.000 description 6
- 238000001035 drying Methods 0.000 description 5
- -1 polypropylene Polymers 0.000 description 5
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- 238000005452 bending Methods 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 238000013329 compounding Methods 0.000 description 3
- 239000003365 glass fiber Substances 0.000 description 3
- 239000011256 inorganic filler Substances 0.000 description 3
- 229910003475 inorganic filler Inorganic materials 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920001955 polyphenylene ether Polymers 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 125000000732 arylene group Chemical group 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 239000012760 heat stabilizer Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 229920005604 random copolymer Polymers 0.000 description 2
- 239000012779 reinforcing material Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- YMTYZTXUZLQUSF-UHFFFAOYSA-N 3,3'-Dimethylbisphenol A Chemical compound C1=C(O)C(C)=CC(C(C)(C)C=2C=C(C)C(O)=CC=2)=C1 YMTYZTXUZLQUSF-UHFFFAOYSA-N 0.000 description 1
- SDDLEVPIDBLVHC-UHFFFAOYSA-N Bisphenol Z Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)CCCCC1 SDDLEVPIDBLVHC-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- OJMOMXZKOWKUTA-UHFFFAOYSA-N aluminum;borate Chemical compound [Al+3].[O-]B([O-])[O-] OJMOMXZKOWKUTA-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000010102 injection blow moulding Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000113 methacrylic resin Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001643 poly(ether ketone) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Supply And Installment Of Electrical Components (AREA)
Abstract
(57)【要約】
【課題】耐熱性、成形性に優れ、帯電防止性もしくは導
電性を有する熱可塑性樹脂組成物およびIC用耐熱トレ
ーを提供すること。
【解決手段】芳香族ポリカーボネート樹脂15〜55重
量%と芳香族ポリサルホン樹脂85〜45重量%からな
る樹脂成分100重量部に対し、炭素繊維5〜65重量
部を配合してなる熱可塑性樹脂組成物、およびそれを成
形してなるIC用耐熱トレー。(57) [Problem] To provide a thermoplastic resin composition having excellent heat resistance and moldability, having antistatic properties or conductivity, and a heat resistant tray for IC. A thermoplastic resin composition comprising 5 to 65 parts by weight of carbon fiber with respect to 100 parts by weight of a resin component comprising 15 to 55% by weight of an aromatic polycarbonate resin and 85 to 45% by weight of an aromatic polysulfone resin. And a heat-resistant tray for ICs obtained by molding the same.
Description
【0001】[0001]
【発明の属する技術分野】本発明は、帯電防止性もしく
は導電性を有する熱可塑性樹脂組成物およびIC用耐熱
トレーに関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an antistatic or conductive thermoplastic resin composition and a heat-resistant tray for IC.
【0002】[0002]
【従来の技術】IC部品(チップ)を搬送するトレーと
しては、従来から導電性もしくは帯電防止性を付与させ
た塩化ビニル樹脂、ポリスチレン樹脂、ポリプロピレン
樹脂などが使われていた。IC部品をハンダによりプリ
ント基板上に実装する際、ICのパッケージが吸湿して
いるとハンダ熱によりIC内部に水蒸気が発生し、フク
レ、クラックなどを生じIC部品が破損するので、実装
前に120〜150℃の温度で水分を除去する必要があ
る。従来、この乾燥工程においては、IC部品を搬送用
トレーからアルミダイカスト製トレーに移し替える必要
があった。ところが、近年この搬送用と乾燥用を兼用で
きるトレーが導電性もしくは帯電防止性を付与させた変
成ポリフェニレンエーテル樹脂で開発され普及してい
る。しかし、そのIC部品の乾燥に要する時間を短縮化
する場合、例えば、150℃以上の高い乾燥温度が必要
となるが、変成ポリフェニレンエーテル樹脂からなるト
レーでは、その耐熱性、成形品の反りや成形加工性など
の面で満足するものが得られなかった。2. Description of the Related Art As a tray for transporting IC parts (chips), a vinyl chloride resin, a polystyrene resin, a polypropylene resin or the like having conductivity or antistatic property has been conventionally used. When mounting an IC component on a printed circuit board by soldering, if the IC package absorbs moisture, solder heat generates water vapor inside the IC, causing blisters, cracks, etc., and breaking the IC component. It is necessary to remove water at a temperature of ~ 150 ° C. Conventionally, in this drying step, it was necessary to transfer the IC parts from the transport tray to an aluminum die-cast tray. However, in recent years, trays that can be used for both transport and drying have been developed and spread from modified polyphenylene ether resins having conductivity or antistatic properties. However, in order to shorten the time required for drying the IC component, a high drying temperature of, for example, 150 ° C. or more is required. However, in the case of a tray made of denatured polyphenylene ether resin, the heat resistance, the warpage of the molded product and the molding Satisfactory workability was not obtained.
【0003】一方、芳香族ポリカーボネート樹脂は機械
強度、寸法精度に優れた樹脂であるが、耐熱性が高々1
50℃である。そこで、その耐熱性などを向上させる目
的で芳香族ポリカーボネート樹脂と芳香族ポリサルホン
樹脂とを混合してなる熱可塑性樹脂組成物が種々開示さ
れている。例えば、特公昭45−39181号公報に
は、芳香族ポリサルホン樹脂と芳香族ポリカーボネート
樹脂とを混合することによって、耐熱性や機械的特性に
優れた組成物が得られることが開示されている。また、
特公昭49−13855号公報には、芳香族ポリサルホ
ン樹脂および芳香族ポリカーボネート樹脂からなる組成
物はABS樹脂に比べて耐熱性や機械的特性に優れるこ
とが開示されている。また、特開昭54−28361号
公報には、重量平均分子量が60000より大きい芳香
族ポリカーボネート樹脂と芳香族ポリサルホン樹脂から
なる組成物は各樹脂に比べて耐薬品性や荷重たわみ温度
が改良されることが開示されている。また、特開昭60
−51739号公報には、特定の構造を有する芳香族ポ
リサルホン樹脂と芳香族ポリカーボネート樹脂からなる
組成物は機械的性質に優れ耐薬品性が改良されることが
開示されている。しかしながら、上記で述べたこれらの
組成物は、芳香族ポリカーボネート樹脂が芳香族ポリサ
ルホン樹脂の本来有する耐熱性に代表される優れた物性
を阻害するため満足できる物性が得られないことが多
い。また、上記の各公報には、その組成物をIC用耐熱
トレーに使用することについての記載はない。On the other hand, aromatic polycarbonate resin is a resin having excellent mechanical strength and dimensional accuracy, but has heat resistance of at most 1.
50 ° C. Therefore, various thermoplastic resin compositions obtained by mixing an aromatic polycarbonate resin and an aromatic polysulfone resin for the purpose of improving the heat resistance and the like have been disclosed. For example, Japanese Patent Publication No. 45-39181 discloses that a composition having excellent heat resistance and mechanical properties can be obtained by mixing an aromatic polysulfone resin and an aromatic polycarbonate resin. Also,
Japanese Patent Publication No. 49-13855 discloses that a composition comprising an aromatic polysulfone resin and an aromatic polycarbonate resin is superior in heat resistance and mechanical properties to ABS resin. JP-A-54-28361 discloses that a composition comprising an aromatic polycarbonate resin and an aromatic polysulfone resin having a weight average molecular weight of more than 60,000 has improved chemical resistance and deflection temperature under load as compared with each resin. It is disclosed. Also, Japanese Patent Application Laid-Open
JP-A-51739 discloses that a composition comprising an aromatic polysulfone resin and an aromatic polycarbonate resin having a specific structure has excellent mechanical properties and improved chemical resistance. However, these compositions described above often fail to provide satisfactory physical properties because the aromatic polycarbonate resin inhibits the excellent physical properties represented by the inherent heat resistance of the aromatic polysulfone resin. Further, each of the above publications does not describe the use of the composition in a heat-resistant tray for IC.
【0004】[0004]
【発明が解決しようとする課題】本発明は、耐熱性、成
形性に優れ、帯電防止性もしくは導電性を有する熱可塑
性樹脂組成物およびIC用耐熱トレーを提供することを
目的とするものである。SUMMARY OF THE INVENTION An object of the present invention is to provide a thermoplastic resin composition having excellent heat resistance and moldability, having antistatic properties or conductivity, and a heat resistant tray for IC. .
【0005】[0005]
【課題を解決するための手段】本発明者らは、上記課題
を解決するために鋭意検討した結果、特定量の芳香族ポ
リカーボネート樹脂と芳香族ポリサルホン樹脂、および
特定量の炭素繊維を選択し、組成物とすることにより上
記目的が達成されることを見出し、本発明に到達した。
すなわち、本発明は次のとおりである。 (1)芳香族ポリカーボネート樹脂15〜55重量%と
芳香族ポリサルホン樹脂85〜45重量%からなる樹脂
成分100重量部に対し、炭素繊維5〜65重量部を配
合してなる熱可塑性樹脂組成物。 (2)下記に定義される芳香族ポリカーボネート樹脂の
溶融粘度(ηa)と芳香族ポリサルホン樹脂の溶融粘度
(ηb)の比(ηa/ηb)が0.5〜2.0である
(1)記載の熱可塑性樹脂組成物。 ηa:340℃、せん断速度1216/秒で測定したと
きの芳香族ポリカーボネート樹脂の溶融粘度。 ηb:340℃、せん断速度1216/秒で測定したと
きの芳香族ポリサルホン樹脂の溶融粘度。 (3)ηa/ηbが0.8〜1.8である(2)記載の熱
可塑性樹脂組成物。 (4)芳香族ポリカーボネート樹脂が、その製造原料と
してビスフェノールAを少なくとも30mol%以上を
用いるコポリカーボネートもしくはホモポリカーボネー
トである(1)、(2)または(3)記載の熱可塑性樹
脂組成物。 (5)芳香族ポリサルホン樹脂が次式Means for Solving the Problems As a result of intensive studies to solve the above-mentioned problems, the present inventors have selected a specific amount of aromatic polycarbonate resin and aromatic polysulfone resin, and a specific amount of carbon fiber, The inventors have found that the above object can be achieved by forming a composition, and have reached the present invention.
That is, the present invention is as follows. (1) A thermoplastic resin composition obtained by blending 5 to 65 parts by weight of carbon fiber with 100 parts by weight of a resin component comprising 15 to 55% by weight of an aromatic polycarbonate resin and 85 to 45% by weight of an aromatic polysulfone resin. (2) the ratio of the melt viscosity of the aromatic polycarbonate resin as defined below (eta a) and the melt viscosity of the aromatic polysulfone resin (η b) (η a / η b) is a 0.5 to 2.0 The thermoplastic resin composition according to (1). η a : melt viscosity of the aromatic polycarbonate resin measured at 340 ° C. and a shear rate of 1216 / sec. η b : melt viscosity of the aromatic polysulfone resin measured at 340 ° C. and a shear rate of 1216 / sec. (3) The thermoplastic resin composition according to (2), wherein η a / η b is 0.8 to 1.8. (4) The thermoplastic resin composition according to (1), (2) or (3), wherein the aromatic polycarbonate resin is a copolycarbonate or a homopolycarbonate using at least 30 mol% of bisphenol A as a raw material for producing the aromatic polycarbonate resin. (5) The aromatic polysulfone resin has the following formula
【0006】[0006]
【化2】 で表される繰り返し単位を80mol%以上有すること
を特徴とする(1)、(2)、(3)または(4)記載
の熱可塑性樹脂組成物。 (6)上記(1)、(2)、(3)、(4)または
(5)記載の熱可塑性樹脂組成物を成形してなるIC用
耐熱トレー。Embedded image The thermoplastic resin composition according to (1), (2), (3) or (4), which has a repeating unit represented by (1) of 80 mol% or more. (6) A heat-resistant tray for IC formed by molding the thermoplastic resin composition according to (1), (2), (3), (4) or (5).
【0007】[0007]
【発明の実施の形態】本発明で用いられる芳香族ポリカ
ーボネート樹脂は、一般式、BEST MODE FOR CARRYING OUT THE INVENTION The aromatic polycarbonate resin used in the present invention has a general formula:
【0008】[0008]
【化3】 で表される繰り返し単位を有する単独重合体、共重合体
およびその混合物である。式中、Aは原料の二価フェノ
ールの残基である二価芳香族基である。このような芳香
族ポリカーボネートを製造するために用いることのでき
る二価フェノールは、官能基として芳香族の炭素原子に
直接結合している2つの水酸基を含有する単核または多
核芳香族化合物である。二価フェノールの例としては、
2,2−ビス(4−ヒドロキシフェニル)プロパン(ビ
スフェノールA)、ビス(4−ヒドロキシフェニル)メ
タン、2,2−ビス(4−ヒドロキシ−3−メチルフェ
ニル)プロパン、2,2−(3,5,3’,5’−テト
ラクロロ−4,4’−ヒドロキシフェニル)プロパン、
2,2−(3,5,3’,5’−テトラブロモ−4,
4’−ヒドロキシフェニル)プロパン、1,1−ビス
(4−ヒドロキシフェニル)シクロヘキサン、ハイドロ
キノン、レゾルシノール、ジヒドロキシジフェニルなど
が挙げられるが、これらに限定されるものではない。ま
た、この芳香族ポリカーボネート樹脂はビスフェノール
Aを少なくとも30mol%以上を用いるコポリカーボ
ネートもしくはホモポリカーボネートであることが好ま
しい。その末端構造は、各々の製法に従って決まるもの
であり、例えば、OHやOC(CH3)3などが挙げられ
るが、これらに限定されるものではない。市販品の例と
しては、住友ダウ株式会社の商品名 カリバー200−
3などがあげられるが、これらに限定されるものではな
い。本発明で用いられる芳香族ポリカーボネート樹脂の
340℃、せん断速度1216/秒で測定したときの溶
融粘度は2000〜10000poiseであることが
好ましく、2000〜6000poiseであることが
より好ましい。溶融粘度が10000poiseを越え
る場合、組成物の溶融粘度が高いために成形加工が困難
となるため好ましくない。Embedded image And a mixture thereof having a repeating unit represented by the formula: In the formula, A is a divalent aromatic group which is a residue of a raw material dihydric phenol. The dihydric phenols that can be used to produce such aromatic polycarbonates are mononuclear or polynuclear aromatic compounds containing two hydroxyl groups that are directly bonded to aromatic carbon atoms as functional groups. Examples of dihydric phenols include:
2,2-bis (4-hydroxyphenyl) propane (bisphenol A), bis (4-hydroxyphenyl) methane, 2,2-bis (4-hydroxy-3-methylphenyl) propane, 2,2- (3 5,3 ′, 5′-tetrachloro-4,4′-hydroxyphenyl) propane,
2,2- (3,5,3 ′, 5′-tetrabromo-4,
Examples include, but are not limited to, 4'-hydroxyphenyl) propane, 1,1-bis (4-hydroxyphenyl) cyclohexane, hydroquinone, resorcinol, dihydroxydiphenyl, and the like. The aromatic polycarbonate resin is preferably a copolycarbonate or homopolycarbonate using at least 30 mol% of bisphenol A. The terminal structure is determined according to each production method, and includes, for example, OH and OC (CH 3 ) 3 , but is not limited thereto. An example of a commercially available product is Sumitomo Dow Co., Ltd. product name Caliber 200-
3 and the like, but are not limited thereto. The melt viscosity of the aromatic polycarbonate resin used in the present invention when measured at 340 ° C. and a shear rate of 1216 / sec is preferably 2,000 to 10,000 poise, more preferably 2,000 to 6,000 poise. If the melt viscosity exceeds 10,000 poise, molding is difficult because the melt viscosity of the composition is high.
【0009】本発明で用いられる芳香族ポリサルホン樹
脂は、アリーレン単位、エーテル結合およびスルホン結
合の三者が必須の構成単位であって、アリーレン単位が
エーテルおよびスルホン結合とともに無秩序にまたは秩
序正しく位置するポリアリーレン化合物として定義され
る。代表的な例としては次のような繰り返し単位を有す
るものがあげられるが、これに限定されるものではな
い。The aromatic polysulfone resin used in the present invention is a polystyrene in which an arylene unit, an ether bond and a sulfone bond are essential constituent units, and the arylene unit is located randomly or orderly together with the ether and sulfone bonds. Defined as an arylene compound. Representative examples include those having the following repeating units, but are not limited thereto.
【0010】[0010]
【化4】 [(II)の化合物はランダム共重合体を含む。式中、
R1 は炭素原子数1ないし6のアルキル基、炭素原子数
3ないし10のアルケニル基、フェニル基またはハロゲ
ン原子を表し、pは0ないし4の正数である。m、nは
平均の繰り返し単位数を示しm、nは0.1から100
の正数である。同一または異なる核上の各R1 は相互に
異なっていても良い。各pは相互に異なっていても良
い。]Embedded image [The compound (II) includes a random copolymer. Where:
R1 represents an alkyl group having 1 to 6 carbon atoms, an alkenyl group having 3 to 10 carbon atoms, a phenyl group or a halogen atom, and p is a positive number of 0 to 4. m and n indicate the average number of repeating units, and m and n are from 0.1 to 100.
Is a positive number. Each R1 on the same or different nuclei may be different from each other. Each p may be different from each other. ]
【0011】[0011]
【化5】 (この化合物はランダム共重合体を含む。式中、R1 は
炭素原子数1ないし6のアルキル基、炭素原子数3ない
し10のアルケニル基、フェニル基またはハロゲン原子
を表し、pは0ないし4の正数である。q、m、nは平
均の繰り返し単位数を示し、qは1〜3の正数、m、n
は0.1〜100の正数である。同一または異なる核上
の各R1 は相互に異なっていても良い。各pは相互に異
なっていても良い。) 本発明で用いられる芳香族ポリサルホン樹脂としては、
(II)または(III)で表される繰り返し単位中の
(m/m+n)は0.8以上であることが好ましい。ま
た、(III)の構造単位中のqは1であることが好ま
しい。これらの中でも(I)、(II)の繰り返し構造
単位を持つものが好ましく、さらに好ましくは(I)の
繰り返し構造単位を持つものである。市販品の例として
は、(I)のものは、住友化学工業株式会社の商品名ス
ミカエクセルPES3600P、4100Pなどが、
(II)のものはAMOCO社の商品名UDELPー1
700などが挙げられるがこれらに限定されるものでは
ない。また、その末端構造は、各々の樹脂の製法に従っ
て決まるものであり、例えば、Cl、OH,OR(Rは
アルキル基)などが挙げられるが、これらに限定される
ものではない。Embedded image (This compound includes a random copolymer. In the formula, R 1 represents an alkyl group having 1 to 6 carbon atoms, an alkenyl group having 3 to 10 carbon atoms, a phenyl group or a halogen atom, and p represents 0 to 4 Q, m, and n indicate the average number of repeating units, and q is a positive number of 1 to 3, m, and n.
Is a positive number from 0.1 to 100. Each R1 on the same or different nuclei may be different from each other. Each p may be different from each other. The aromatic polysulfone resin used in the present invention includes:
(M / m + n) in the repeating unit represented by (II) or (III) is preferably 0.8 or more. Further, q in the structural unit of (III) is preferably 1. Among these, those having a repeating structural unit of (I) and (II) are preferable, and those having a repeating structural unit of (I) are more preferable. As examples of commercially available products, those of (I) include Sumika Excel PES3600P, 4100P, etc., which are trade names of Sumitomo Chemical Co., Ltd.
(II) is AMOCO's trade name UDELP-1
700 and the like, but are not limited to these. Further, the terminal structure is determined according to the production method of each resin, and includes, for example, Cl, OH, OR (R is an alkyl group) and the like, but is not limited thereto.
【0012】本発明で用いられる芳香族ポリサルホン樹
脂の340℃、せん断速度1216/秒で測定したとき
の溶融粘度は1000〜6000poiseであること
が好ましく、1000〜3000poiseであること
がより好ましい。溶融粘度が6000poiseを越え
る場合、組成物の溶融粘度が高いために成形加工が困難
となるため好ましくない。本発明で用いられる芳香族ポ
リカーボネート樹脂(a)と芳香族ポリサルホン樹脂
(b)の、340℃、せん断速度1216/秒で測定し
たときの溶融粘度の比(ηa/ηb)は0.5〜2.0で
あることが好ましく、0.8〜1.8であることがより
好ましく、さらに好ましくは1.0〜1.6である。本
発明の樹脂組成物に配合される芳香族ポリカーボネート
樹脂の配合量は、芳香族ポリサルホン樹脂と芳香族ポリ
カーボネート樹脂の全重量を基にして15〜55重量%
であり、25〜45重量%であることがより好ましい。
芳香族ポリカーボネート樹脂を55重量%より多く配合
すると、組成物の耐熱性が劣るためにましくない。The melt viscosity of the aromatic polysulfone resin used in the present invention, when measured at 340 ° C. and a shear rate of 1216 / sec, is preferably from 1,000 to 6000 poise, more preferably from 1,000 to 3,000 poise. If the melt viscosity exceeds 6000 poise, the composition has a high melt viscosity, which makes molding difficult, which is not preferable. The melt viscosity ratio (η a / η b ) of the aromatic polycarbonate resin (a) and the aromatic polysulfone resin (b) used in the present invention measured at 340 ° C. and a shear rate of 1216 / sec is 0.5. It is preferably from 2.0 to 2.0, more preferably from 0.8 to 1.8, and even more preferably from 1.0 to 1.6. The amount of the aromatic polycarbonate resin blended in the resin composition of the present invention is 15 to 55% by weight based on the total weight of the aromatic polysulfone resin and the aromatic polycarbonate resin.
And more preferably 25 to 45% by weight.
If the amount of the aromatic polycarbonate resin is more than 55% by weight, the heat resistance of the composition is inferior.
【0013】本発明で用いる炭素繊維は、化学組成の9
0%以上が炭素よりなる繊維状物質であり、原料として
はポリアクリロニトリル、ピッチ、再生セルロースなど
を用いることができる。これらの原料を用いて紡糸され
た繊維状前駆体を1000〜2000℃で処理したも
の、あるいは2000〜3000℃で黒鉛化したものが
高強度、高弾性を示すため一般に用いられる。本発明で
用いられる炭素繊維の繊維長や繊維径は特に限定されな
いが、繊維長30μm〜6mm、繊維径5〜20μmの
ものが一般に用いられる。市販品の例としては、東邦レ
ーヨン株式会社の商品名 ベスファイトHTA−C6−
CS、HTA−CMF−0160N/S、株式会社ドナ
ックの商品名 ドナカーボS−231、S−244など
があげられるが、これらに限定されるものではない。本
発明で用いられる炭素繊維の配合量は、芳香族ポリカー
ボネート樹脂と芳香族ポリサルホン樹脂からなる樹脂成
分100重量部に対し5〜65重量部である。炭素繊維
の配合量が5重量部より少ないとIC用耐熱トレーに求
められる帯電防止性が満足されないため好ましくなく、
65重量部より多いと組成物の溶融粘度が高くなるため
にICトレーへ加工することが困難になったり、ICト
レーの反りを生じたりするために好ましくない。The carbon fiber used in the present invention has a chemical composition of 9%.
0% or more is a fibrous substance composed of carbon, and polyacrylonitrile, pitch, regenerated cellulose or the like can be used as a raw material. A fibrous precursor spun using these raw materials, which has been treated at 1000 to 2000 ° C or graphitized at 2000 to 3000 ° C, is generally used because it exhibits high strength and high elasticity. Although the fiber length and fiber diameter of the carbon fiber used in the present invention are not particularly limited, those having a fiber length of 30 μm to 6 mm and a fiber diameter of 5 to 20 μm are generally used. As an example of a commercially available product, Toho Rayon Co., Ltd. product name Vesfight HTA-C6-
CS, HTA-CMF-0160N / S, and Donac Corporation's trade names Donacarbo S-231 and S-244, but are not limited thereto. The compounding amount of the carbon fiber used in the present invention is 5 to 65 parts by weight based on 100 parts by weight of the resin component composed of the aromatic polycarbonate resin and the aromatic polysulfone resin. If the compounding amount of the carbon fiber is less than 5 parts by weight, the antistatic property required for the heat resistant tray for IC is not satisfied, which is not preferable.
If the amount is more than 65 parts by weight, the melt viscosity of the composition becomes high, making it difficult to process into an IC tray and causing the IC tray to warp.
【0014】本発明においては、必要に応じてガラス繊
維、シリカアルミナ繊維、アルミナ繊維、ホウ酸アルミ
ニウムウィスカーなどの繊維状あるいは針状の補強剤、
タルク、マイカ、クレー、ガラスビーズなどの無機充填
剤、フッ素樹脂などや金属石鹸類などの離型改良材、染
料、顔料などの着色剤、酸化防止剤、熱安定剤、紫外線
吸収剤、界面活性剤などの通常の添加剤を1種以上添加
することができる。また、少量の熱可塑性樹脂、例え
ば、ポリエチレン、ポリプロピレン、ポリ塩化ビニル、
ABS樹脂、ポリスチレン、メタクリル樹脂、ポリアミ
ド、ポリエステル、ポリフェニレンスルフィド、ポリエ
ーテルケトン、ポリフェニレンエーテルおよびその変成
物、ポリエーテルイミドなど、少量の熱硬化性樹脂、た
とえば、フェノール樹脂、エポキシ樹脂、シアネート樹
脂、イソシアネート樹脂、ポリイミド樹脂などや、少量
のゴム成分などの一種または二種以上を添加することも
できる。本発明の樹脂組成物を得るための原材料の配合
手段は特に限定されない。芳香族ポリカーボネート樹
脂、芳香族ポリサルホン樹脂、必要に応じてガラス繊維
などの補強材や無機充填材、離型改良剤、熱安定剤など
をヘンシェルミキサー、タンブラー等を用いて混合した
後、押出機を用いて溶融混練することが一般的である。
そのときの溶融混練法としては、すべての原材料を一括
して混合した後で押出機へフィードしてもかまわない
し、必要に応じてガラス繊維などの補強材や無機充填材
などの原材料を、樹脂を主体とする原材料とは別にフィ
ードしてもかまわない。本発明の熱可塑性樹脂組成物を
用いて成形する成形体の作成方法は特に限定されない。
樹脂を溶融し賦形、固化せしめる方法としては押出成
形、射出成形、ブロー成形などが挙げられるが、この中
では特に射出成形が好ましく用いられる。また、押出成
形された成形品を、切削やプレスによって加工しても良
い。本発明のIC用耐熱トレー(チップトレーともい
う)としては、正方形ポケット付トレー、長方形ポケッ
ト付トレー等が挙げられる。本発明の熱可塑性樹脂組成
物は、 IC用耐熱トレー以外に、自動車、航空機等の
部品、産業用機器、家電製品、食器や医療機器、OA、
AV機器、電子、電子部品、例えば、特に耐熱性が必要
とされる、半導体ウエハーキャリヤー、LCDキャリヤ
ー、TABテープキャリヤー、ICソケットなどの成形
材料として好適に用いることができる。In the present invention, a fibrous or acicular reinforcing agent such as glass fiber, silica alumina fiber, alumina fiber, aluminum borate whisker, etc.
Inorganic fillers such as talc, mica, clay, and glass beads; release improvers such as fluororesins and metal soaps; coloring agents such as dyes and pigments; antioxidants; heat stabilizers; ultraviolet absorbers; One or more ordinary additives such as an agent can be added. Also, a small amount of thermoplastic resin, for example, polyethylene, polypropylene, polyvinyl chloride,
A small amount of thermosetting resin such as ABS resin, polystyrene, methacrylic resin, polyamide, polyester, polyphenylene sulfide, polyether ketone, polyphenylene ether and its modified product, polyetherimide, for example, phenol resin, epoxy resin, cyanate resin, isocyanate One or more of a resin, a polyimide resin, and a small amount of a rubber component can be added. The means for compounding the raw materials for obtaining the resin composition of the present invention is not particularly limited. After mixing an aromatic polycarbonate resin, an aromatic polysulfone resin, a reinforcing material such as glass fiber, an inorganic filler, a release improver, a heat stabilizer, etc. using a Henschel mixer, a tumbler, etc., the extruder is used. It is common to melt-knead the mixture.
The melt-kneading method at this time may be such that all the raw materials are mixed at once and then fed to an extruder.If necessary, raw materials such as reinforcing materials such as glass fibers and inorganic fillers may be mixed with resin. It may be fed separately from raw materials mainly composed of. The method for producing a molded article molded using the thermoplastic resin composition of the present invention is not particularly limited.
Methods for melting, shaping, and solidifying the resin include extrusion molding, injection molding, and blow molding. Of these, injection molding is particularly preferably used. The extruded molded article may be processed by cutting or pressing. Examples of the heat-resistant tray for an IC (also referred to as a chip tray) of the present invention include a tray with a square pocket and a tray with a rectangular pocket. The thermoplastic resin composition of the present invention can be used in addition to heat-resistant trays for ICs, parts for automobiles, aircraft, etc., industrial equipment, home appliances, tableware and medical equipment, OA,
It can be suitably used as a molding material for AV equipment, electronics, and electronic components, for example, semiconductor wafer carriers, LCD carriers, TAB tape carriers, IC sockets, etc., which particularly require heat resistance.
【0015】[0015]
【実施例】以下、本発明の実施例を示すが、本発明はこ
れらに限定されるものではない。なお、実施例中の溶融
粘度、荷重たわみ温度、Izod衝撃強度、曲げ強度、
および表面固有抵抗の測定は、次の方法で行った。 (1)溶融粘度:本発明の熱可塑性樹脂組成物に用いる
芳香族ポリカーボネート樹脂と芳香族ポリサルホン樹脂
の溶融粘度は、(株)東洋精機製作所製キャピログラフ
1Bを用いて、ダイ径1mm、340℃、せん断速度1
216/秒で測定した。 (2)荷重たわみ温度:本発明の熱可塑性樹脂組成物か
ら、射出成形機を用いて長さ127mm、幅12.7m
m、厚み6.4mmの試験片を成形し、ASTM D6
48に準拠し18.6kg/cm2の荷重で測定した。 (3)Izod衝撃強度 上記(2)の試験片を2等分してIzod衝撃強度測定
用の試験片とし、ASTM D−256に準拠して測定
した。 (4)曲げ強度 上記(2)の試験片を用いて曲げ強度測定用の試験片と
し、ASTM D−790に準拠して測定した。 (5)表面固有抵抗 本発明の熱可塑性樹脂組成物から、射出成形機を用いて
1辺64mm、厚み3mmの試験片を成形し、絶縁抵抗
計(三和計器製作所製 PDM−256)で電圧250
Vで測定した。EXAMPLES Examples of the present invention will be shown below, but the present invention is not limited to these examples. The melt viscosity, deflection temperature under load, Izod impact strength, bending strength,
The measurement of the surface resistivity was performed by the following method. (1) Melt viscosity: The melt viscosity of the aromatic polycarbonate resin and the aromatic polysulfone resin used in the thermoplastic resin composition of the present invention was determined using a Capillograph 1B manufactured by Toyo Seiki Seisaku-Sho, Ltd., with a die diameter of 1 mm and 340 ° C. Shear speed 1
Measured at 216 / sec. (2) Deflection temperature under load: 127 mm in length and 12.7 m in width from the thermoplastic resin composition of the present invention using an injection molding machine.
m, a test piece having a thickness of 6.4 mm was formed and subjected to ASTM D6
The measurement was performed at a load of 18.6 kg / cm 2 in accordance with No.48. (3) Izod impact strength The test piece of the above (2) was divided into two equal parts to obtain a test piece for measuring Izod impact strength, which was measured in accordance with ASTM D-256. (4) Bending strength The test piece of (2) was used as a test piece for measuring bending strength, and measured in accordance with ASTM D-790. (5) Surface Specific Resistance From the thermoplastic resin composition of the present invention, a test piece having a side length of 64 mm and a thickness of 3 mm was molded using an injection molding machine, and the voltage was measured with an insulation resistance meter (PDM-256 manufactured by Sanwa Keiki Seisakusho). 250
Measured in V.
【0016】実施例1〜5、比較例1〜3 芳香族ポリカーボネート樹脂(住友ダウ株式会社製、商
品名カリバー)、芳香族ポリサルホン樹脂(住友化学工
業株式会社製、商品名スミカエクセルPES)および炭
素繊維(東邦レーヨン(株)製、商品名ベスファイトHT
A−C6−CS)を表1に示す組成でヘンシェルミキサ
ーで混合後、二軸押出機(池貝鉄工(株)製、PCM−3
0)を用いてシリンダー温度340℃で造粒し、熱可塑
性樹脂組成物を得た。なお、各樹脂成分の重量%は、樹
脂成分の合計量をベースとする。また、樹脂成分以外の
成分の重量部は、樹脂成分100重量部当りの割合であ
る。それぞれの樹脂の溶融粘度は上記の方法で測定し
た。この熱可塑性樹脂組成物を、射出成形機(日精樹脂
工業(株)製PS40E5ASE)を用いてシリンダー温
度350℃、金型温度120℃で上記の試験片を成形
し、荷重たわみ温度、Izod衝撃強度、曲げ強度、お
よび表面固有抵抗の測定を行い、結果を表2に示した。Examples 1 to 5, Comparative Examples 1 to 3 Aromatic polycarbonate resin (manufactured by Sumitomo Dow Co., trade name: Caliber), aromatic polysulfone resin (manufactured by Sumitomo Chemical Co., Ltd., trade name: Sumika Excel PES) and carbon Textile (Vesfight HT, manufactured by Toho Rayon Co., Ltd.)
A-C6-CS) with the composition shown in Table 1 using a Henschel mixer, followed by a twin-screw extruder (PCM-3, manufactured by Ikegai Iron Works Co., Ltd.).
Using 0), the mixture was granulated at a cylinder temperature of 340 ° C. to obtain a thermoplastic resin composition. The weight% of each resin component is based on the total amount of the resin components. The parts by weight of the components other than the resin component are ratios per 100 parts by weight of the resin component. The melt viscosity of each resin was measured by the method described above. The test piece was molded from the thermoplastic resin composition at a cylinder temperature of 350 ° C. and a mold temperature of 120 ° C. using an injection molding machine (PS40E5ASE manufactured by Nissei Resin Industry Co., Ltd.), and the deflection temperature under load and Izod impact strength were measured. , Bending strength, and surface resistivity were measured, and the results are shown in Table 2.
【0017】[0017]
【表1】 [Table 1]
【0018】[0018]
【表2】 [Table 2]
【0019】実施例6 上記の方法で得た実施例2に示す組成の熱可塑性樹脂組
成物を用いて、射出成形機(住友重機械工業製 SG1
50M)を用いてシリンダー温度340℃、金型温度1
50℃、射出速度70%、射出圧力1400kg/cm
2、保持圧力800kg/cm2でICトレー(長さ31
0mm、幅140mm、高さ8mm、平均肉厚1.5m
m)を成形し、反りのない良好な製品を得た。このIC
トレーを熱風循環オーブンで180℃で1時間熱処理し
たところ、反りや変形は生じなかった。Example 6 An injection molding machine (SG1 manufactured by Sumitomo Heavy Industries, Ltd.) was used using the thermoplastic resin composition having the composition shown in Example 2 obtained by the above method.
50M), cylinder temperature 340 ° C, mold temperature 1
50 ° C, injection speed 70%, injection pressure 1400kg / cm
2. IC tray (length 31) with holding pressure 800 kg / cm 2
0mm, width 140mm, height 8mm, average thickness 1.5m
m) to obtain a good product without warpage. This IC
When the tray was heat-treated in a hot air circulating oven at 180 ° C. for 1 hour, no warping or deformation occurred.
【0020】[0020]
【発明の効果】本発明の熱可塑性樹脂組成物は、耐熱性
や機械的物性に優れており、それから成形されたIC用
耐熱トレーは、高温でのICの乾燥に耐えることができ
取り扱い性に優れたきわめて有用なものである。The thermoplastic resin composition of the present invention is excellent in heat resistance and mechanical properties, and the heat-resistant tray for IC molded therefrom can withstand drying of IC at high temperature and has good handleability. Excellent and very useful.
Claims (6)
量%と芳香族ポリサルホン樹脂85〜45重量%からな
る樹脂成分100重量部に対し、炭素繊維5〜65重量
部を配合してなる熱可塑性樹脂組成物。1. A thermoplastic resin composition comprising 5 to 65 parts by weight of carbon fiber per 100 parts by weight of a resin component comprising 15 to 55% by weight of an aromatic polycarbonate resin and 85 to 45% by weight of an aromatic polysulfone resin. Stuff.
樹脂の溶融粘度(ηa)と芳香族ポリサルホン樹脂の溶
融粘度(ηb)の比(ηa/ηb)が0.5〜2.0であ
る請求項1記載の熱可塑性樹脂組成物。 ηa:340℃、せん断速度1216/秒で測定したと
きの芳香族ポリカーボネート樹脂の溶融粘度。 ηb:340℃、せん断速度1216/秒で測定したと
きの芳香族ポリサルホン樹脂の溶融粘度。Wherein the ratio of the melt viscosity of the aromatic polycarbonate resin as defined below (eta a) and the melt viscosity of the aromatic polysulfone resin (η b) (η a / η b) 0.5 to 2.0 The thermoplastic resin composition according to claim 1, wherein η a : melt viscosity of the aromatic polycarbonate resin measured at 340 ° C. and a shear rate of 1216 / sec. η b : melt viscosity of the aromatic polysulfone resin measured at 340 ° C. and a shear rate of 1216 / sec.
記載の熱可塑性樹脂組成物。3. The method according to claim 2, wherein η a / η b is 0.8 to 1.8.
The thermoplastic resin composition according to the above.
原料としてビスフェノールAを少なくとも30mol%
以上を用いるコポリカーボネートもしくはホモポリカー
ボネートである請求項1、2または3記載の熱可塑性樹
脂組成物。4. An aromatic polycarbonate resin comprising at least 30 mol% of bisphenol A as a raw material for producing the same.
4. The thermoplastic resin composition according to claim 1, which is a copolycarbonate or a homopolycarbonate using the above.
を特徴とする請求項1、2、3または4記載の熱可塑性
樹脂組成物。5. The aromatic polysulfone resin has the following formula: 5. The thermoplastic resin composition according to claim 1, having a repeating unit represented by the formula: 80 mol% or more. 6.
塑性樹脂組成物を成形してなるIC用耐熱トレー。6. A heat-resistant tray for IC formed by molding the thermoplastic resin composition according to claim 1, 2, 3, 4, or 5.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10127293A JPH11323131A (en) | 1998-05-11 | 1998-05-11 | Thermoplastic resin composition and heat-resistant tray for ic |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10127293A JPH11323131A (en) | 1998-05-11 | 1998-05-11 | Thermoplastic resin composition and heat-resistant tray for ic |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH11323131A true JPH11323131A (en) | 1999-11-26 |
Family
ID=14956387
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10127293A Pending JPH11323131A (en) | 1998-05-11 | 1998-05-11 | Thermoplastic resin composition and heat-resistant tray for ic |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH11323131A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002082592A1 (en) * | 2001-04-03 | 2002-10-17 | Kureha Kagaku Kogyo K.K. | Ic socket |
WO2005078008A1 (en) * | 2004-02-16 | 2005-08-25 | Kureha Corporation | Stock shape for machining and production process thereof |
-
1998
- 1998-05-11 JP JP10127293A patent/JPH11323131A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002082592A1 (en) * | 2001-04-03 | 2002-10-17 | Kureha Kagaku Kogyo K.K. | Ic socket |
US7198734B2 (en) | 2001-04-03 | 2007-04-03 | Kureha Corporation | IC socket |
CN1311594C (en) * | 2001-04-03 | 2007-04-18 | 株式会社吴羽 | IC socket |
WO2005078008A1 (en) * | 2004-02-16 | 2005-08-25 | Kureha Corporation | Stock shape for machining and production process thereof |
JP2005226031A (en) * | 2004-02-16 | 2005-08-25 | Kureha Chem Ind Co Ltd | Machine processing material and method for producing the same |
US8158240B2 (en) | 2004-02-16 | 2012-04-17 | Kureha Corporation | Stock shape for machining |
US8158242B2 (en) | 2004-02-16 | 2012-04-17 | Kureha Corporation | Stock shape for machining and production process thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6127492A (en) | Thermoplastic resin composition and heat-resistant tray for IC | |
EP3546509B1 (en) | Thermally conductive thermoplastic compositions with good dielectric property and the shaped article therefore | |
EP0400935B1 (en) | Flame-retardant and glass fiber-reinforced polyester resin molding compositions | |
JP6223531B2 (en) | Polyphenylene sulfide resin composition, method for producing the same, and reflector | |
JP2019500435A (en) | Thermoplastic resin composition and molded article containing the same | |
JP2006328291A (en) | Polyarylene sulfide resin composition and injection molded article | |
JPH01301756A (en) | Aromatic polysulfone resin composition with excellent plating properties | |
EP1799769B1 (en) | Sulfone polymer composition | |
WO2017057903A1 (en) | Glass fiber-reinforced polycarbonate resin composition and molded article using same | |
JPH11323131A (en) | Thermoplastic resin composition and heat-resistant tray for ic | |
KR100606155B1 (en) | Aromatic Polysulfone Resin Compositions and Molded Articles Containing the Same | |
JP2000034408A (en) | Thermoplastic resin composition and molded article thereof | |
JPH11310703A (en) | Thermoplastic resin composition and heat-resistant tray for IC | |
JPH11181284A (en) | Aromatic polysulfone resin composition and molded article thereof | |
KR101854012B1 (en) | Thermoplastic resin composition and article comprising the same | |
JP2702814B2 (en) | Molded product with metal inserted | |
JPH10212403A (en) | Thermoplastic resin composition and molded article | |
KR101146967B1 (en) | Production process tape for film-shaped wiring board | |
KR100513976B1 (en) | Polyphenylene Sulfide Thermoplastic Resin Composition | |
KR20200050064A (en) | Thermoplastic resin composition having excellent impact resistance and fluidity and improved dimensional stability and heat aging property and molded article produced using the same | |
JPH11181255A (en) | Thermoplastic resin composition | |
JP3837870B2 (en) | Thermoplastic resin composition and molded body | |
WO2015046678A1 (en) | Thermoplastic resin composition and molded article comprising same | |
JP2000007914A (en) | Resin composition, molded article and ic tray using the same | |
JPH1196817A (en) | Lamp reflector |