JPH04342754A - Polyester resin composition - Google Patents
Polyester resin compositionInfo
- Publication number
- JPH04342754A JPH04342754A JP14552791A JP14552791A JPH04342754A JP H04342754 A JPH04342754 A JP H04342754A JP 14552791 A JP14552791 A JP 14552791A JP 14552791 A JP14552791 A JP 14552791A JP H04342754 A JPH04342754 A JP H04342754A
- Authority
- JP
- Japan
- Prior art keywords
- resin composition
- polyester
- polyester resin
- repeating unit
- weight
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 15
- 229920001225 polyester resin Polymers 0.000 title claims abstract description 8
- 239000004645 polyester resin Substances 0.000 title claims abstract description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229920000728 polyester Polymers 0.000 claims abstract description 11
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 6
- WSQZNZLOZXSBHA-UHFFFAOYSA-N 3,8-dioxabicyclo[8.2.2]tetradeca-1(12),10,13-triene-2,9-dione Chemical compound O=C1OCCCCOC(=O)C2=CC=C1C=C2 WSQZNZLOZXSBHA-UHFFFAOYSA-N 0.000 claims abstract description 5
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000011256 inorganic filler Substances 0.000 claims abstract description 5
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- -1 polypropylene Polymers 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000003365 glass fiber Substances 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- 239000010456 wollastonite Substances 0.000 description 3
- 229910052882 wollastonite Inorganic materials 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 229920006230 thermoplastic polyester resin Polymers 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene 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
- 239000006230 acetylene black Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 229920003232 aliphatic polyester Polymers 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent 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
- 238000005452 bending Methods 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 210000000078 claw Anatomy 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
- 238000007334 copolymerization reaction Methods 0.000 description 1
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical compound OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920000921 polyethylene adipate Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001955 polyphenylene ether Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は導電性、帯電防止性を付
与し、例えば電子部品の熱処理工程においてキャリアケ
ースとして有用な寸法精度、耐熱性の特に優れた熱可塑
性ポリエステル樹脂組成物に関するものである。[Industrial Application Field] The present invention relates to a thermoplastic polyester resin composition that imparts conductivity and antistatic properties and has particularly excellent dimensional accuracy and heat resistance, which is useful as a carrier case in the heat treatment process of electronic components, for example. be.
【0002】0002
【従来の技術】現在、電子機器の小型化が進むにつれ、
高度実装化が進み、より密度を上げるためにスルーホー
ル基板等にIC部品の実装が行なわれているが、その際
のクローソルダーによるIC部品の実装時の加熱中に、
IC部品が吸湿しているとIC内部にふくれ、クラック
等が生じ、IC部品が破損する。このため実装前には予
め100℃以上の温度でIC部品を乾燥し、水分を除去
しなければならない。[Background Art] Currently, as electronic devices become smaller,
With the advancement of advanced packaging, IC components are mounted on through-hole boards to increase density, but during the heating process when the IC components are mounted using claw solder,
If an IC component absorbs moisture, bulges, cracks, etc. will occur inside the IC, and the IC component will be damaged. Therefore, before mounting, IC components must be dried at a temperature of 100° C. or higher to remove moisture.
【0003】前記IC乾燥工程において従来より用いら
れるキャリアケースとして、導電性を有する塩化ビニル
、ポリスチレン、ポリプロピレン系の樹脂が用いられて
いるが、この場合は100℃以上の耐熱性がないため、
一度アルミダイキャスト製キャリアケースに移して乾燥
した後、前記ケースに再度移してから出荷しており、余
分な工程が必要であった。またキャリアケースとして導
電性を有するポリフェニレンエーテル系の樹脂を用いる
場合は100℃以上の耐熱性があるため、アルミダイキ
ャスト製キャリアケースに移しかえずに乾燥できるが、
120〜130℃程度の温度でしか処理できないので、
72〜96時間もの長い処理時間が必要となり効率的で
なかった。[0003] As carrier cases conventionally used in the IC drying process, conductive resins such as vinyl chloride, polystyrene, and polypropylene are used, but in this case, they do not have heat resistance above 100°C.
After being transferred to an aluminum die-cast carrier case and dried, it was transferred again to the case before being shipped, which required an extra step. In addition, when using conductive polyphenylene ether resin as the carrier case, it has a heat resistance of 100°C or higher, so it can be dried without being transferred to an aluminum die-cast carrier case.
Since it can only be processed at temperatures of around 120-130℃,
It required a long processing time of 72 to 96 hours, which was not efficient.
【0004】その他ポリアミド樹脂はそれ自身、吸湿性
が高く、この用途には不向きであり、またポリカーボネ
ート樹脂は流動性が悪く成形品に反りが生じやすく寸法
安定性に欠ける。その他、高耐熱樹脂としてはポリフェ
ニレンスルフイド、ポリエーテルサルホン、ポリアリレ
ートなどが挙げられるが、いずれも価格が高く、実用化
するに至らなかった。[0004] In addition, polyamide resins themselves have high hygroscopicity and are unsuitable for this purpose, and polycarbonate resins have poor fluidity and tend to warp in molded products, lacking dimensional stability. Other highly heat-resistant resins include polyphenylene sulfide, polyether sulfone, and polyarylate, but all of these are expensive and have not been put into practical use.
【0005】[0005]
【発明が解決しようとする課題】そこで本発明は、15
0℃以上の耐熱性を有し、高価なアルミダイキャスト製
キャリアケースの代替として適した組成物を得ることを
課題とするものであり、この課題を解決できれば、乾燥
の処理温度を150℃以上にすることができ、24時間
位で充分に乾燥が出来るため、アルミダイキャスト製キ
ャリアケースに移しかえる工程の簡略化、乾燥時間の短
縮化など、当業界において寄与すること大である。[Problems to be Solved by the Invention] Therefore, the present invention provides 15
The goal is to obtain a composition that has heat resistance of 0°C or higher and is suitable as a substitute for expensive aluminum die-cast carrier cases.If this problem can be solved, the drying temperature can be increased to 150°C or higher. Since it can be fully dried in about 24 hours, it will greatly contribute to the industry by simplifying the process of transferring to an aluminum die-cast carrier case and shortening the drying time.
【0006】[0006]
【課題を解決するための手段】本発明者らは上記課題を
解決すべく鋭意研究、検討した結果、遂に本発明を完成
するに到った。すなわち本発明はエチレンテレフタレー
トを主たるくり返し単位とするポリエステルおよび/ま
たはブチレンテレフタレートを主たるくり返し単位とす
るポリエステル100重量部、無機充填材5〜40重量
部および導電性カーボン3〜30重量部を含有すること
を特徴とするポリエステル樹脂組成物である。[Means for Solving the Problems] As a result of intensive research and examination in order to solve the above-mentioned problems, the present inventors have finally completed the present invention. That is, the present invention contains 100 parts by weight of a polyester whose main repeating unit is ethylene terephthalate and/or a polyester whose main repeating unit is butylene terephthalate, 5 to 40 parts by weight of an inorganic filler, and 3 to 30 parts by weight of conductive carbon. This is a polyester resin composition characterized by the following.
【0007】本発明において用いられるエチレンテレフ
タレートを主たるくり返し単位とするポリエステルおよ
び/またはブチレンテレフタレートを主たるくり返し単
位とするポリエステルは、酸成分としてテレフタル酸、
グリコール成分としてエチレングリコールおよび/また
はブチレングリコールより得られるが、その他約20モ
ル%以下の共重合成分として、公知の酸成分および/ま
たはグリコール成分が使用できる。例えばイソフタル酸
、ナフタレン1,4または2,6ジカルボン酸、ジフェ
ニールエーテル、4,4ジカルボン酸、アジピン酸、セ
バシン酸のような酸成分、プロピレングリコール、ブチ
レングリコール、ジエチレングリコール、ネオペンチル
グリコール、シクロヘキサンジメタノール、2,2−ビ
ス(4−ヒドロキシフェニル)プロパンのようなグリコ
ール成分、P−オキシ安息香酸、P−ヒドロキシエトキ
シ安息香酸のようなオキシ酸等が挙げられる。本発明で
使用されるエチレンテレフタレートを主たるくり返し単
位とするポリエステルはフェノール/テトラクロロエタ
ン混合溶媒(6/4重量比)により30℃で測定して求
めた固有粘度が通常0.4以上、好ましくは0.5以上
であり、ブチレンテレフタレートを主たるくり返し単位
とするポリエステルの固有粘度は通常0.5以上であり
、好ましくは0.7〜1.3である。The polyester having ethylene terephthalate as the main repeating unit and/or the polyester having butylene terephthalate as the main repeating unit used in the present invention contains terephthalic acid,
The glycol component is obtained from ethylene glycol and/or butylene glycol, but other known acid components and/or glycol components can be used as copolymerization components of about 20 mol% or less. Acid components such as isophthalic acid, naphthalene 1,4 or 2,6 dicarboxylic acids, diphenyl ether, 4,4 dicarboxylic acids, adipic acid, sebacic acid, propylene glycol, butylene glycol, diethylene glycol, neopentyl glycol, cyclohexane dicarboxylic acid, etc. Examples include methanol, glycol components such as 2,2-bis(4-hydroxyphenyl)propane, and oxyacids such as P-oxybenzoic acid and P-hydroxyethoxybenzoic acid. The polyester having ethylene terephthalate as a main repeating unit used in the present invention has an intrinsic viscosity of usually 0.4 or more, preferably 0. The intrinsic viscosity of polyester containing butylene terephthalate as a main repeating unit is usually 0.5 or more, preferably 0.7 to 1.3.
【0008】本発明で用いられる無機充填材としては表
面性質、熱安定性、物性等からタルク、グラファイト、
ワラストナイト、クレー、雲母、モンモリナイト、カオ
リン、珪酸カルシウム、シラスバルーン、ガラス短繊維
、ガラスビーズ、シリカ、石青、二硫化モリブテン、金
属炭化物等が例示されるが、耐熱性、衝撃強度からタル
ク、雲母、ワラストナイトが特に好ましい。該充填材の
粒径は外観および物性から平均30μ以下であることが
好ましい。また本発明においては、さらに繊維状強化材
としてガラス繊維、カーボン繊維、またはグラファイト
繊維、金属炭化物繊維、金属窒化物繊維、アラミド繊維
、フェノール樹脂繊維等を配合してもよく、特にガラス
繊維が好ましい。その直径は通常15μ以下で、プラス
チック強化用の表面処理や集束処理したものが好ましい
。無機充填材は5〜40重量部、好ましくは8〜30重
量部含まれる。5重量部未満では耐熱性が不十分であり
、40重量部を超えると流動性や伸度、たわみが低下し
、良好な成形物が得にくくなる。The inorganic fillers used in the present invention include talc, graphite,
Examples include wollastonite, clay, mica, montmorinite, kaolin, calcium silicate, shirasu balloons, short glass fibers, glass beads, silica, stone blue, molybdenum disulfide, and metal carbides, but talc is preferred due to its heat resistance and impact strength. , mica, and wollastonite are particularly preferred. The particle size of the filler is preferably 30 μm or less on average from the viewpoint of appearance and physical properties. Further, in the present invention, glass fibers, carbon fibers, graphite fibers, metal carbide fibers, metal nitride fibers, aramid fibers, phenolic resin fibers, etc. may be further blended as fibrous reinforcing materials, and glass fibers are particularly preferred. . The diameter thereof is usually 15 μm or less, and it is preferable to have a surface treatment for plastic reinforcement or a focusing treatment. The inorganic filler is contained in an amount of 5 to 40 parts by weight, preferably 8 to 30 parts by weight. If it is less than 5 parts by weight, heat resistance will be insufficient, and if it exceeds 40 parts by weight, fluidity, elongation, and deflection will decrease, making it difficult to obtain a good molded product.
【0009】本発明における導電性カーボンとは、樹脂
中に充填することにより高い導電性を付与し、樹脂の表
面抵抗を大幅に低下するものであり、アセチレンブラッ
クおよびファーネスブラック等が好ましく用いられる。
ファーネスブラックとしては具体的にはケッチェンブラ
ックEC(オランダ・アクゾ社商品名)、HS−500
(旭カーボン社商品名)、バルカンXC72(米国CA
BOT社商品名)等の市販品がある。本発明において導
電性カーボンは3〜30重量部、好しくは4〜20重量
部含まれる。3重量部未満では導電性が不十分であり、
30重量部を超えると流動性や機械強度が低下し、良好
な成形物が得にくくなる。[0009] The conductive carbon in the present invention imparts high conductivity when filled into a resin and significantly reduces the surface resistance of the resin, and acetylene black, furnace black, etc. are preferably used. Specifically, the furnace blacks include Ketjenblack EC (product name of Akzo, Netherlands) and HS-500.
(Asahi Carbon Co., Ltd. product name), Vulcan XC72 (USA CA
There are commercially available products such as BOT (trade name). In the present invention, the conductive carbon is contained in an amount of 3 to 30 parts by weight, preferably 4 to 20 parts by weight. If it is less than 3 parts by weight, the conductivity is insufficient;
If it exceeds 30 parts by weight, fluidity and mechanical strength will decrease, making it difficult to obtain a good molded product.
【0010】本発明のポリエステル樹脂組成物には目的
、用途に応じて、公知の酸化防止剤、紫外線吸収剤、可
塑剤、滑剤、難燃剤、帯電防止剤、離型剤、着色剤等の
添加剤を配合してもよく、またポリエチレンナフタレー
ト等の芳香族ポリエステルやポリブチレンアジペート、
ポリエチレンアジペート、ポリラクトン等の脂肪族ポリ
エステルやポリカーボネート等の他の熱可塑性樹脂を混
合してもよい。Depending on the purpose and use, the polyester resin composition of the present invention may contain known antioxidants, ultraviolet absorbers, plasticizers, lubricants, flame retardants, antistatic agents, mold release agents, colorants, etc. Aromatic polyesters such as polyethylene naphthalate, polybutylene adipate,
Other thermoplastic resins such as aliphatic polyesters such as polyethylene adipate and polylactone, and polycarbonate may be mixed.
【0011】なお本発明組成物を得る方法としては、特
に制限されるものではなく任意の方法で行われる。例え
ば、全成分を予備混合した後、押出機やニーダ中で混練
する方法や、予め任意の成分を押出機やニーダ中で混練
配合して得たペレットに、更に残りの成分を溶融混合す
る方法等が挙げられる。また本発明のポリエステル樹脂
組成物にて成形品を製造するに際しては、特殊な成形法
や成形条件は必要でなく、通常の熱可塑性ポリエステル
樹脂の成形条件によって充分成形することが出き、板状
、容器等の各種成形品とされる。[0011] The composition of the present invention can be obtained by any method without particular limitation. For example, a method in which all components are premixed and then kneaded in an extruder or kneader, or a method in which arbitrary components are kneaded and blended in an extruder or kneader in advance, resulting in pellets, and then the remaining components are melt-mixed. etc. In addition, when producing molded products using the polyester resin composition of the present invention, no special molding method or molding conditions are required, and the molding can be performed satisfactorily under the molding conditions of ordinary thermoplastic polyester resins, and it is possible to form a plate-shaped product. , various molded products such as containers.
【0012】0012
【実施例】以下、実施例により本発明をより具体的に説
明する。なお得られた組成物の特性は以下の方法によっ
て評価した。
(1) 熱変形温度
曲げ応力4.6kg/cm2 としてASTM D−
648に準拠した。
(2) 成形品(ICキャリアケース)の変形及び反
り300×150mmのキャリアケースを150℃24
時間乾燥機の中に放置した後、平板の上に置き、変形、
および反りを観察した。(2mm以下を合格とする)(
3) 成形品の機械強度
高さ2mからコンクリート上に自然落下させ、破損の有
無を観察した。
(4) 成形品の表面固有抵抗
2点端子表面固有抵抗測定器にて測定した。[Examples] The present invention will be explained in more detail with reference to Examples below. Note that the properties of the obtained composition were evaluated by the following method. (1) ASTM D- as heat deformation temperature bending stress 4.6kg/cm2
648. (2) Deformation and warpage of molded product (IC carrier case) A carrier case of 300 x 150 mm was heated at 150°C at 24°C.
After leaving it in the dryer for an hour, place it on a flat plate to deform and
and warping was observed. (2mm or less is considered acceptable) (
3) Mechanical strength of the molded product The molded product was allowed to fall naturally onto concrete from a height of 2 m and the presence or absence of damage was observed. (4) Surface specific resistance of molded product Measured using a two-point terminal surface specific resistance measuring device.
【0013】実施例1〜8、比較例1〜5ポリエチレン
テレフタレート樹脂(極限粘度0.62)、ポリブチレ
ンテレフタレート樹脂(極限粘度1.1)、ガラス繊維
、タルク、ワラストナイト、ケッチェンブラックECを
“表1”に示す割合で予備混合した後、2軸押出機のホ
ッパーに投入し、シリンダー温度270℃にて溶融混練
してコンパウンドチップを得た。このコンパウンドチッ
プを130℃で4時間乾燥した後、シリンダー温度26
0−265−270℃に調節した射出成形機によりテス
トピース、及びICキャリアケースを成形した。その特
性評価を“表1”に併記する。Examples 1 to 8, Comparative Examples 1 to 5 Polyethylene terephthalate resin (intrinsic viscosity 0.62), polybutylene terephthalate resin (intrinsic viscosity 1.1), glass fiber, talc, wollastonite, Ketjenblack EC After premixing in the proportions shown in Table 1, the mixture was charged into a hopper of a twin-screw extruder and melt-kneaded at a cylinder temperature of 270°C to obtain compound chips. After drying this compound chip at 130℃ for 4 hours, the cylinder temperature was 26℃.
A test piece and an IC carrier case were molded using an injection molding machine adjusted to 0-265-270°C. The characteristic evaluation is also listed in "Table 1".
【表1】[Table 1]
【0014】[0014]
【発明の効果】“表1”より明らかなように、本発明組
成物は熱変形温度が高く成形加工性に優れ、150℃以
上の高温下においても変形や反りがなく、表面固有抵抗
値が107 Ω以下であることが判る。従って本発明ポ
リエステル樹脂組成物は、導電性、帯電防止性を有し、
寸法精度、耐熱性に優れているため、特に電子部品等の
キャリアケースとして有用である。Effects of the Invention As is clear from Table 1, the composition of the present invention has a high heat distortion temperature, excellent moldability, no deformation or warping even at high temperatures of 150°C or higher, and a low specific surface resistance value. It can be seen that it is less than 107 Ω. Therefore, the polyester resin composition of the present invention has electrical conductivity and antistatic properties,
Due to its excellent dimensional accuracy and heat resistance, it is particularly useful as a carrier case for electronic components.
Claims (1)
返し単位とするポリエステルおよび/またはブチレンテ
レフタレートを主たるくり返し単位とするポリエステル
100重量部、無機充填材5〜40重量部および導電性
カーボン3〜30重量部を含有することを特徴とするポ
リエステル樹脂組成物。Claim 1: Contains 100 parts by weight of a polyester whose main repeating unit is ethylene terephthalate and/or a polyester whose main repeating unit is butylene terephthalate, 5 to 40 parts by weight of an inorganic filler, and 3 to 30 parts by weight of conductive carbon. A polyester resin composition characterized by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14552791A JPH04342754A (en) | 1991-05-20 | 1991-05-20 | Polyester resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14552791A JPH04342754A (en) | 1991-05-20 | 1991-05-20 | Polyester resin composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04342754A true JPH04342754A (en) | 1992-11-30 |
Family
ID=15387284
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14552791A Pending JPH04342754A (en) | 1991-05-20 | 1991-05-20 | Polyester resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04342754A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000034381A1 (en) * | 1998-12-09 | 2000-06-15 | General Electric Company | Conductive, low warp polyetherimide resin compositions |
JP2005213331A (en) * | 2004-01-28 | 2005-08-11 | Mitsubishi Gas Chem Co Inc | Polyester resin composition |
-
1991
- 1991-05-20 JP JP14552791A patent/JPH04342754A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000034381A1 (en) * | 1998-12-09 | 2000-06-15 | General Electric Company | Conductive, low warp polyetherimide resin compositions |
US6610773B1 (en) | 1998-12-09 | 2003-08-26 | General Electric Company | Conductive, low warp polyetherimide resin compositions |
JP2005213331A (en) * | 2004-01-28 | 2005-08-11 | Mitsubishi Gas Chem Co Inc | Polyester resin composition |
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