JP4303015B2 - Flame retardant aromatic polycarbonate resin composition - Google Patents

Description

【００５３】
（但し上記式中のＸは、ハイドロキノン、レゾルシノール、ビス（４−ヒドロキシジフェニル）メタン、ビスフェノールＡ、ジヒドロキシジフェニル、ジヒドロキシナフタレン、ビス（４−ヒドロキシフェニル）スルホン、ビス（４−ヒドロキシフェニル）ケトン、ビス（４−ヒドロキシフェニル）サルファイドから誘導される２価の基が挙げられ、ｊ、ｋ、ｌ、ｍはそれぞれ独立して０または１であり、ｎは０〜５の整数であり、またはｎ数の異なるリン酸エステルの混合物の場合は０〜５の平均値であり、Ｒ¹、Ｒ²、Ｒ³、およびＲ⁴はそれぞれ独立して１個以上のハロゲン原子を置換したもしくは置換していないフェノール、クレゾール、キシレノール、イソプロピルフェノール、ブチルフェノール、ｐ−クミルフェノールから誘導される１価の基である。）
さらに好ましいものとしては、上記式中のＸが、ハイドロキノン、レゾルシノール、ビスフェノールＡ、およびジヒドロキシジフェニルから誘導される２価の基が挙げられ、ｊ、ｋ、ｌ、ｍはそれぞれ１であり、ｎは１〜３の整数であり、またはｎ数の異なるリン酸エステルのブレンドの場合はその平均値であり、Ｒ¹、Ｒ²、Ｒ³、およびＲ⁴はそれぞれ独立して１個以上のハロゲン原子を置換したもしくはより好適には置換していないフェノール、クレゾール、キシレノールから誘導される１価の基である。
【００５４】
また、Ｄ成分の有機リン化合物は、そのＴＧＡによる、窒素ガス雰囲気中における２３℃から２０℃／分の昇温速度で６００℃まで昇温した時の５％重量減少温度が２８０℃以上であるものが好ましい。該重量減少温度はさらに、３２０℃以上がより好ましく、３３０℃以上がさらに好ましく、３４０℃以上が特に好ましい。該重量減少温度の上限としては３８０℃以下が一般に入手可能で適切であり、３７０℃以下がより適切である。上記の如く重量減少温度が比較的高温の有機リン化合物は、樹脂組成物の溶融粘度の低下効果と共に、良好な耐熱性（良好な荷重たわみ温度など）を樹脂組成物に付与できる点で好ましい。
【００５５】
上記の点などを考慮すると、上記式のリン酸エステルの中でも、レゾルシノールビス（ジキシレニルホスフェート）を主体とするリン酸エステルオリゴマー、４，４−ジヒドロキシジフェニルビス（ジキシレニルホスフェート）を主体とするリン酸エステルオリゴマー、およびビスフェノールＡビス（ジフェニルホスフェート）を主体とするリン酸エステルオリゴマーが好適である（ここで主体とするとは、重合度の異なる他の成分を少量含んでよいことを示す）。
【００５６】
本発明の樹脂組成物は、含フッ素滴下防止剤（Ｅ成分）を含有している。この含フッ素滴下防止剤（Ｅ成分）の含有により、成形品の物性を損なうことなく、良好な難燃性を達成することができる。
【００５７】
Ｅ成分としての含フッ素滴下防止剤としては、フィブリル形成能を有する含フッ素ポリマーを挙げることができ、かかるポリマーとしてはポリテトラフルオロエチレン、テトラフルオロエチレン系共重合体（例えば、テトラフルオロエチレン／ヘキサフルオロプロピレン共重合体、など）、米国特許第４３７９９１０号公報に示されるような部分フッ素化ポリマー、フッ素化ジフェノールから製造されるポリカーボネート樹脂などを挙げることができる。中でも好ましくはポリテトラフルオロエチレン（以下ＰＴＦＥと称することがある）である。
【００５８】
フィブリル形成能を有するＰＴＦＥの分子量は極めて高い分子量を有し、せん断力などの外的作用によりＰＴＦＥ同士を結合して繊維状になる傾向を示すものである。その分子量は、標準比重から求められる数平均分子量において１００万〜１０００万、より好ましく２００万〜９００万である。かかるＰＴＦＥは、固体形状の他、水性分散液形態のものも使用可能である。またかかるフィブリル形成能を有するＰＴＦＥは樹脂中での分散性を向上させ、さらに良好な難燃性および機械的特性を得るために他の樹脂との混合形態のＰＴＦＥ混合物を使用することも可能である。
【００５９】
かかるフィブリル形成能を有するＰＴＦＥの市販品としては例えば三井・デュポンフロロケミカル（株）のテフロン６Ｊ、ダイキン工業（株）のポリフロンＭＰＡ ＦＡ５００およびＦ−２０１Ｌなどを挙げることができる。ＰＴＦＥの水性分散液の市販品としては、旭アイシーアイフロロポリマーズ（株）製のフルオンＡＤ−１、ＡＤ−９３６、ダイキン工業（株）製のフルオンＤ−１およびＤ−２、三井・デュポンフロロケミカル（株）製のテフロン３０Ｊなどを代表として挙げることができる。
【００６０】
混合形態のＰＴＦＥとしては、（１）ＰＴＦＥの水性分散液と有機重合体の水性分散液または溶液とを混合し共沈殿を行い共凝集混合物を得る方法（特開昭６０−２５８２６３号公報、特開昭６３−１５４７４４号公報などに記載された方法）、（２）ＰＴＦＥの水性分散液と乾燥した有機重合体粒子とを混合する方法（特開平４−２７２９５７号公報に記載された方法）、（３）ＰＴＦＥの水性分散液と有機重合体粒子溶液を均一に混合し、かかる混合物からそれぞれの媒体を同時に除去する方法（特開平０６−２２０２１０号公報、特開平０８−１８８６５３号公報などに記載された方法）、（４）ＰＴＦＥの水性分散液中で有機重合体を形成する単量体を重合する方法（特開平９−９５５８３号公報に記載された方法）、および（５）ＰＴＦＥの水性分散液と有機重合体分散液を均一に混合後、さらに該混合分散液中でビニル系単量体を重合し、その後混合物を得る方法（特開平１１−２９６７９号などに記載された方法）により得られたものが使用できる。これらの混合形態のＰＴＦＥの市販品としては、三菱レイヨン（株）の「メタブレン Ａ３０００」（商品名）、およびＧＥスペシャリティーケミカルズ社製 「ＢＬＥＮＤＥＸ Ｂ４４９」（商品名）などを挙げることができる。
【００６１】
混合形態におけるＰＴＦＥの割合としては、ＰＴＦＥ混合物１００重量％中、ＰＴＦＥが１〜６０重量％が好ましく、より好ましくは５〜５５重量％である。ＰＴＦＥの割合がかかる範囲にある場合は、ＰＴＦＥの良好な分散性を達成することができる。なお、上記Ｅ成分の割合は正味の含フッ素滴下防止剤の量を示し、混合形態のＰＴＦＥの場合には、正味のＰＴＦＥ量を示す。
【００６２】
本発明の樹脂組成物は、さらに一価または多価アルコールと高級脂肪酸とのエステル（Ｆ成分）を任意成分として含有することが好ましい。Ｆ成分の使用により本発明の前記した効果を維持しつつ、さらに優れた離型性をも有する樹脂組成物が提供される。その結果より良好な寸法安定性を有する成形品が提供される。殊に本発明においてより好適なＤ成分を含有する場合に、かかるＦ成分の好ましい効果が特に発揮される。より好適なＤ成分については前記のとおりである。
【００６３】
Ｆ成分のエステルを構成する高級脂肪酸は、好ましくは炭素数２０以上（より好ましくは炭素数２０〜３２、さらに好ましくは炭素数２６〜３２）の脂肪酸を６０重量％以上含有する。かかる高級脂肪酸として、モンタン酸を主成分とする高級脂肪酸が好ましく例示される。かかる高級脂肪酸は通常モンタンロウを酸化することにより製造される。
【００６４】
Ｆ成分を構成する一価アルコールとしては、例えばドデカノール、テトラデカノール、ヘキサデカノール、オクタデカノール、エイコサノール、テトラコサノール、セリルアルコール、およびトリアコンタノールなどが例示される。
【００６５】
Ｆ成分を構成する多価アルコールとしては、例えばエチレングリコール、グリセリン、ジグリセリン、ポリグリセリン（例えばデカグリセリンなど）、ペンタエリスリトール、ジペンタエリスリトール、トリメチロールプロパン、ジエチレングリコール、およびプロピレングリコールなどが挙げられる。これらの中でもエチレングリコール、グリセリン、ペンタエリスリトール、ジペンタエリスリトール、およびトリメチロールプロパンが好ましく、特にエチレングリコールが好ましい。
【００６６】
モンタン酸を主成分とする高級脂肪酸と一価または多価アルコール（好ましくは多価アルコール）とのエステルは、密度：０．９４〜１．１０ｇ／ｃｍ³、酸価：１〜２００、鹸化価：５０〜２００の範囲であることが好適であり、より好適には、密度：０．９８〜１．０６ｇ／ｃｍ³、酸価：５〜３０、鹸化価：１００〜１８０の範囲である。
【００６７】
次に本発明の樹脂組成物を構成するＡ〜Ｅ成分および任意成分としてのＦ成分の割合について説明する。
【００６８】
本発明の樹脂組成物において、樹脂成分である芳香族ポリカーボネート樹脂（Ａ成分）およびアクリロニトリル−スチレン共重合体（Ｂ成分；ＡＳ樹脂）の合計量は、Ａ成分、Ｂ成分、Ｃ成分およびＤ成分の合計１００重量％当り５０重量％以上であり、好ましくは６０重量％以上である。Ａ成分とＢ成分の合計量の上限は、Ｃ成分およびＤ成分の割合により主として左右されるが、８０重量％、好ましくは７６重量％が適当である。
【００６９】
Ａ成分およびＢ成分の両者の割合は、Ａ成分およびＢ成分の合計１００重量部当り、Ａ成分７５〜９５重量部でありかつＢ成分は５〜２５重量部であり、好ましくはＡ成分７８〜９２重量部でありかつＢ成分８〜２２重量部である。
【００７０】
無機充填材（Ｃ成分）の割合は、Ｃ−１成分およびＣ−２成分の合計として、Ａ〜Ｄ成分の合計１００重量％当り、１５〜３５重量％、好ましくは２０〜３０重量％である。またＡ〜Ｄ成分の合計１００重量％当り、Ｃ−１成分は１０〜２５重量％、好ましくは１０〜２０重量％、特に好ましくは１２〜２０重量％であり、Ｃ−２成分は３〜１５重量％、好ましくは５〜１５重量％、特に好ましくは５〜１２重量％である。Ｃ−１成分とＣ−２成分との両者の割合は、Ｃ−１成分とＣ−２成分の合計１００重量部当り、Ｃ−１成分が４０〜９０重量部でありかつＣ−２成分が６０〜１０重量部であり、好ましくはＣ−１成分が５０〜８０重量部でありかつＣ−２成分が５０〜２０重量部である。
【００７１】
難燃剤としての有機リン化合物（Ｄ成分）は、Ａ〜Ｄ成分の合計１００重量％当り、３〜１５重量％、好ましくは３〜１０重量％、更に好ましくは３〜６重量％である。
【００７２】
含フッ素滴下防止剤（Ｅ成分）は、Ａ〜Ｄ成分１００重量部当り、０．０２〜２重量部、好ましくは０．０５〜２重量部、より好ましくは０．１〜１重量部、更に好ましくは０．１５〜０．８重量部である。また離型剤としての高級脂肪酸エステル（Ｆ成分）は、Ａ〜Ｄ成分の合計１００重量部当り、２重量部以下、好ましくは０．０１〜２重量部、より好ましくは０．０５〜１．５重量部であり、特に好ましくは０．１〜１．０重量部である。
【００７３】
本発明の樹脂組成物は、前記したＡ〜Ｆ成分の組合せおよびその組成割合であることによって、その組成物からの成形品は、優れた物理的特性を有しかつ難燃性に優れている。すなわち、成形品の衝撃強度（Ｊ／ｍ）は３０以上であり、好適には３５以上を示し、その上限は好適には５５にも達する。また成形品の収縮異方性（成形品の流れ方向と直角方向における成形収縮率（％）の差の絶対値）が小さく０．１５以下、好適には０．１０以下の値を有する。
【００７４】
本発明の樹脂組成物からの成形品は、難燃剤（Ｄ成分）の含有割合が比較的に少ないにもかかわらず、ＵＬ９４規格による１．６ｍｍ厚の試験片の難燃テストにおいてＶ−１レベルを達成することができる。
【００７５】
また本発明の成形品は、Ｂ成分、無機充填材のＣ−１成分およびＣ−２成分、並びにＤ成分の組合せによって、高剛性かつ低比重の樹脂組成物を提供する。かかる比重はより具体的には、真密度で示して１．３〜１．４５（ｇ／ｃｍ³）、好適条件下では１．３２〜１．４０（ｇ／ｃｍ³）である。
【００７６】
本発明のＡ成分〜Ｅ成分からなる樹脂組成物、およびＡ成分〜Ｆ成分からなる樹脂組成物からの成形品は、低粘度潤滑油に対して良好な耐性を有する。シャーシ成形品に組み付けられる各種機構部品が滑らかに作動するよう、シャーシ成形品は予め潤滑油を塗布される場合があり、または使用中に塗布される可能性を有する。したがって、かかる良好な耐性は、シャーシ成形品に必要とされる好ましい特性である。
【００７７】
低粘度潤滑油は、炭化水素油、シリコーン油、フッ素油などが例示される。本発明のＡ成分〜Ｅ成分からなる樹脂組成物、およびＡ成分〜Ｆ成分からなる樹脂組成物からの成形品は、これらの中でも広範に使用される炭化水素油に対して良好な耐性を有し、中でも使用頻度の高いパラフィン油を主成分とする潤滑油に対して良好な耐性を有する。
【００７８】
前記低粘度潤滑油は、４０℃において２〜２０ｍｍ²／ｓの範囲の動粘度を有するものであり、より好適には２〜１０ｍｍ²／ｓの範囲の動粘度を有するものである。低粘度潤滑油の具体例としては、例えば呉工業（株）製ＣＲＣ５−５６などが例示される。
【００７９】
本発明の樹脂組成物は、無機充填材（Ｃ成分）としてＣ−１成分およびＣ−２成分の組合せを使用することに起因して、金型の摩耗性が極めて少なく成形コストを低減できるという利点を有している。
【００８０】
本発明の樹脂組成物は、前記したＡ〜Ｆ成分の割合を維持しかつ目的を損なわない限り他の成分を含有していてもよい。例えばＡ成分およびＢ成分以外の他の熱可塑性樹脂としては、例えば、ポリエチレン樹脂、ポリプロピレン樹脂、ポリアルキルメタクリレート樹脂、ポリアセタール樹脂、ポリアルキレンテレフタレート樹脂、ポリアミド樹脂、環状ポリオレフィン樹脂、ポリアリレート樹脂（非晶性ポリアリレート、液晶性ポリアリレート）、ポリエーテルエーテルケトン、ポリエーテルイミド、ポリアミドイミドなどに代表される各種熱可塑性ポリイミド、ポリサルフォン、ポリエーテルサルフォン、ポリフェニレンサルファイドなどを挙げることができる。これらは目的に応じて上記Ａ成分およびＢ成分と併用して使用することができる。殊にポリアリレート樹脂は制振性が要求される場合に、良好な難燃性と制振性を両立できることから併用して使用することが好ましい場合がある。
【００８１】
更に本発明の難燃性熱可塑性樹脂組成物は、少量のゴム質重合体を含むことができる。かかる割合は、Ａ成分〜Ｄ成分の合計１００重量部に対して１．５重量部以下とすることが適切であり、より好ましくは１．３重量部以下、更に好ましくは１重量部以下である。
【００８２】
ゴム質重合体としてより具体的には、ＳＢ（スチレン−ブタジエン）重合体、ＡＢＳ（アクリロニトリル−ブタジエン−スチレン）重合体、ＭＢＳ（メチルメタクリレート−ブタジエン−スチレン）重合体、ＭＡＢＳ（メチルメタクリレート−アクリロニトリル−ブタジエン−スチレン）重合体、ＭＢ（メチルメタクリレート−ブタジエン）重合体、ＡＳＡ（アクリロニトリル−スチレン−アクリルゴム）重合体、ＡＥＳ（アクリロニトリル−エチレンプロピレンゴム−スチレン）重合体、ＭＡ（メチルメタクリレート−アクリルゴム）重合体、ＭＡＳ（メチルメタクリレート−アクリルゴム−スチレン）重合体、メチルメタクリレート−アクリル・ブタジエンゴム共重合体、メチルメタクリレート−アクリル・ブタジエンゴム−スチレン共重合体、メチルメタクリレート−（アクリル・シリコーンＩＰＮゴム）重合体などを挙げることができる。これらの重合体はいずれもゴム成分からなる重合体のコアに上記単量体からなるポリマー鎖が結合したコア−シェルタイプのグラフト共重合体であることが好ましい。
【００８３】
尚、本発明のゴム質重合体は、他の成分中に含有される形態であってもよい。かかる形態のゴム質重合体としては、例えばＡＢＳ樹脂中に含まれるＡＢＳ共重合体が例示される。
【００８４】
本発明でＤ成分の有機リン化合物以外の難燃剤としては、赤リン系難燃剤、ハロゲン系難燃剤、シリコーン系難燃剤、および金属塩系難燃剤などを挙げることができる。しかしながら、本発明においては、難燃剤として実質的にＤ成分のみを含有するものが好適である。
【００８５】
本発明は、本発明の目的を損なわない範囲においてＣ−１成分およびＣ−２成分以外の無機充填材を少量含むことも可能である。ここでガラス繊維やガラスフレークなどのガラス系充填材（モース硬度約６．５）や、ホウ酸アルミニウムウイスカー（モース硬度約７）および酸化チタン（ルチル型でモース硬度約７）などの硬度の高い充填材は、その割合がＡ成分〜Ｄ成分の合計１００重量部に対して３重量部以下とすることが適切であり、１重量部以下がより好ましい。一方、モース硬度が５以下の充填材であれば、３重量部を超えて配合することも可能であるが、５重量部以下とすることが好ましい。
【００８６】
本発明の樹脂組成物には、他に熱安定剤、酸化防止剤、紫外線吸収剤、離型剤（Ｆ成分以外）、帯電防止剤、発泡剤、染顔料（殊にカーボンブラック、酸化チタン等）等を配合することもできる。
【００８７】
熱安定剤としては、亜リン酸、リン酸、亜ホスホン酸、ホスホン酸およびこれらのエステル等のリン系の熱安定剤が挙げられ、具体的には、トリフェニルホスファイト、トリスノニルフェニルホスファイト、トリス（２，４−ジ−ｔｅｒｔ−ブチルフェニル）ホスファイト、トリデシルホスファイト、トリオクチルホスファイト、トリオクタデシルホスファイト、ジデシルモノフェニルホスファイト、ジオクチルモノフェニルホスファイト、ジイソプロピルモノフェニルホスファイト、モノブチルジフェニルホスファイト、モノデシルジフェニルホスファイト、モノオクチルジフェニルホスファイト、ビス（２，６−ジ−ｔｅｒｔ−ブチル−４−メチルフェニル）ペンタエリスリトールジホスファイト、２，２−メチレンビス（４，６−ジ−ｔｅｒｔ−ブチルフェニル）オクチルホスファイト、ビス（ノニルフェニル）ペンタエリスリトールジホスファイト、ビス（２，４−ジ−ｔｅｒｔ−ブチルフェニル）ペンタエリスリトールジホスファイト等の亜リン酸エステル化合物、トリブチルホスフェート、トリメチルホスフェート、トリクレジルホスフェート、トリフェニルホスフェート、トリクロルフェニルホスフェート、トリエチルホスフェート、ジフェニルクレジルホスフェート、ジフェニルモノオルソキセニルホスフェート、トリブトキシエチルホスフェート、ジブチルホスフェート、ジオクチルホスフェート、ジイソプロピルホスフェート等のリン酸エステル化合物、さらにその他のリン系熱安定剤として、テトラキス（２，４−ジ−ｔｅｒｔ−ブチルフェニル）−４，４’−ビフェニレンジホスホナイト、テトラキス（２，４−ジ−ｔｅｒｔ−ブチルフェニル）−４，３’−ビフェニレンジホスホナイト、テトラキス（２，４−ジ−ｔｅｒｔ−ブチルフェニル）−３，３’−ビフェニレンジホスホナイト、ビス（２，４−ジ−ｔｅｒｔ−ブチルフェニル）−４−ビフェニレンホスホナイト等の亜ホスホン酸エステル化合物等を挙げることができる。これらのうち、トリスノニルフェニルホスファイト、ジステアリルペンタエリスリトールジホスファイト、ビス（２，４−ジ−ｔｅｒｔ−ブチルフェニル）ペンタエリスリトールジホスファイト、トリス（２，４−ジ−ｔｅｒｔ−ブチルフェニル）ホスファイト、トリフェニルホスフェート、トリメチルホスフェート、テトラキス（２，４−ジ−ｔｅｒｔ−ブチルフェニル）−４，４’−ビフェニレンジホスホナイト、ビス（２，４−ジ−ｔｅｒｔ−ブチルフェニル）−４−ビフェニレンホスホナイトが好ましい。これらの熱安定剤は、単独でもしくは２種以上混合して用いてもよい。かかる熱安定剤の配合量は、Ａ成分〜Ｄ成分の合計１００重量部に対して０．０００１〜１重量部が好ましく、０．０００５〜０．５重量部がより好ましく、０．００２〜０．３重量部がさらに好ましい。
【００８８】
酸化防止剤としては、例えばペンタエリスリトールテトラキス（３−メルカプトプロピオネート）、ペンタエリスリトールテトラキス（３−ラウリルチオプロピオネート）、グリセロール−３−ステアリルチオプロピオネート、トリエチレングリコール−ビス［３−（３−ｔ−ブチル−５−メチル−４−ヒドロキシフェニル）プロピオネート］、１，６−ヘキサンジオール−ビス［３−（３，５−ジ−ｔ−ブチル−４−ヒドロキシフェニル）プロピオネート］、ペンタエリスリトール−テトラキス［３−（３，５−ジ−ｔ−ブチル−４−ヒドロキシフェニル）プロピオネート］、オクタデシル−３−（３，５−ジ−ｔ−ブチル−４−ヒドロキシフェニル）プロピオネート、１，３，５−トリメチル−２，４，６−トリス（３，５−ジ−ｔ−ブチル−４−ヒドロキシベンジル）ベンゼン、Ｎ，Ｎ−ヘキサメチレンビス（３，５−ジ−ｔ−ブチル−４−ヒドロキシ−ヒドロシンナマイド）、３，５−ジ−ｔ−ブチル−４−ヒドロキシ−ベンジルホスホネート−ジエチルエステル、トリス（３，５−ジ−ｔ−ブチル−４−ヒドロキシベンジル）イソシアヌレート、４，４’−ビフェニレンジホスホスフィン酸テトラキス（２，４−ジ−ｔ−ブチルフェニル）、３，９−ビス｛１，１−ジメチル−２−［β−（３−ｔ−ブチル−４−ヒドロキシ−５−メチルフェニル）プロピオニルオキシ］エチル｝−２，４，８，１０−テトラオキサスピロ（５，５）ウンデカン等が挙げられる。これら酸化防止剤の配合量は、Ａ成分〜Ｄ成分の合計１００重量部に対して０．０００１〜０．０５重量部が好ましい。
【００８９】
紫外線吸収剤としては、例えば２，２’−ジヒドロキシ−４−メトキシベンゾフェノンに代表されるベンゾフェノン系紫外線吸収剤、および例えば２−（３−ｔｅｒｔ−ブチル−５−メチル−２−ヒドロキシフェニル）−５−クロロベンゾトリアゾール、２−（３，５−ジ−ｔｅｒｔ−ブチル−２−ヒドロキシフェニル）−５−クロロベンゾトリアゾール、２，２’−メチレンビス［４−（１，１，３，３−テトラメチルブチル）−６−（２Ｈ−ベンゾトリアゾール−２−イル）フェノール］、２−［２−ヒドロキシ−３，５−ビス（α，α−ジメチルベンジル）フェニル］−２Ｈ−ベンゾトリアゾールおよび２−（３，５−ジ−ｔｅｒｔ−アミル−２−ヒドロキシフェニル）ベンゾトリアゾールに代表されるベンゾトリアゾール系紫外線吸収剤が例示される。さらにビス（２，２，６，６−テトラメチル−４−ピペリジル）セバケート、ビス（１，２，２，６，６−ペンタメチル−４−ピペリジル）セバケート等に代表されるヒンダードアミン系の光安定剤も使用することが可能である。かかる紫外線吸収剤、光安定剤の配合量は、Ａ成分〜Ｄ成分の合計１００重量部に対して０．０１〜５重量部が好ましい。
【００９０】
Ｆ成分以外の離型剤としては、オレフィン系ワックス、シリコーンオイル、フッ素オイル、オルガノポリシロキサン、パラフィンワックス、および蜜蝋等が挙げられる。
【００９１】
帯電防止剤としては、例えばポリエーテルエステルアミド、グリセリンモノステアレート、ドデシルベンゼンスルホン酸アンモニウム塩、ドデシルベンゼンスルホン酸ホスホニウム塩、無水マレイン酸モノグリセライド、無水マレイン酸ジグリセライド等が挙げられる。かかる帯電防止剤の配合量は、Ａ成分〜Ｄ成分の合計１００重量部に対して０．５〜２０重量部が好ましい。
【００９２】
本発明者はさらに研究を進めたところ、前記した樹脂組成物の利点および効果は、樹脂成分がポリフェニレンエーテル樹脂およびポリスチレン樹脂である樹脂組成物においても同様に達成されることが見出された。
【００９３】
かくして本発明によれば、
（１）ポリフェニレンエーテル樹脂（Ｐ成分）、
（２）ポリスチレン樹脂（Ｓ成分）、
（３）無機充填材（Ｃ成分）、
（４）有機リン化合物系難燃剤（Ｄ成分）および
（５）含フッ素滴下防止剤（Ｅ成分）
よりなり、これら各成分の割合は、下記（ｉ）〜（iii）の条件を満足することを特徴とする難燃性芳香族ポリフェニレンエーテル樹脂組成物（以下“ＰＰＥ樹脂組成物”という）が提供される。
（ｉ）Ｐ、Ｓ、ＣおよびＤ成分の合計１００重量％当り、Ｐ成分およびＳ成分の合計は５０重量％以上であり、Ｃ成分は１５〜３５重量％であり、Ｄ成分は３〜１５重量％であり、かつＰ、Ｓ、ＣおよびＤ成分の合計１００重量部当りＥ成分は０〜２重量部である、
（ii）Ｐ成分およびＳ成分の合計１００重量部当り、Ｐ成分は５０〜８５重量部であり、かつＳ成分は１５〜５０重量部である、
（iii）Ｃ成分は（Ｃ１）平均粒子径３０〜３００μｍのマイカ（Ｃ−１成分）および（Ｃ２）タルクおよびワラストナイトからなる群から選択される少なくとも１種の充填材（Ｃ−２成分）より構成され、Ｐ、Ｓ、ＣおよびＤ成分の合計１００重量％当り、Ｃ−１成分は１０〜２５重量％であり、Ｃ−２成分は３〜１５重量％でありかつＣ−１成分およびＣ−２成分の合計１００重量部当りＣ−１成分は４０〜９０重量部である。
【００９４】
このＰＰＥ樹脂組成物におけるポリフェニレンエーテル樹脂（Ｐ成分）とは、フェニレンエーテル構造を有する核置換フェノールの重合体または共重合体（以下単にＰＰＥ重合体と称する場合がある）である。
【００９５】
フェニレンエーテル構造を有する核置換フェノールの重合体の代表例としては、ポリ（２，６−ジメチル−１，４−フェニレン）エーテル、ポリ（２−メチル−６−エチル−１，４−フェニレン）エーテル、ポリ（２，６−ジエチル−１，４−フェニレン）エーテル、ポリ（２−エチル−６−ｎ−プロピル−１，４−フェニレン）エーテル、ポリ（２，６−ジ−ｎ−プロピル−１，４−フェニレン）エーテル、ポリ（２−メチル−６−ｎ−ブチル−１，４−フェニレン）エーテル、ポリ（２−エチル−６−イソプロピル−１，４−フェニレン）エーテル、ポリ（２−メチル−６−ヒドロキシエチル−１，４−フェニレン）エーテル、ポリ（２−メチル−６−クロロエチル−１，４−フェニレン）エーテル等が挙げられる。この中で、ポリ（２，６−ジメチル−１，４−フェニレン）エーテルが特に好ましい。
【００９６】
フェニレンエーテル構造を有する核置換フェノールの共重合体の代表例としては、２，６−ジメチルフェノールと２，３，６−トリメチルフェノールとの共重合体、２，６−ジメチルフェノールとｏ−クレゾールとの共重合体あるいは２，６−ジメチルフェノールと２，３，６−トリメチルフェノールおよびｏ−クレゾールとの共重合体等がある。
【００９７】
上記のＰＰＥ重合体の製造方法は特に限定されるものではないが例えば米国特許４，７８８，２７７号明細書（特願昭６２−７７５７０号）に記載されている方法に従って、ジブチルアミンの存在下に、２，６−キシレノールを酸化カップリング重合して製造することができる。
【００９８】
また、ＰＰＥ重合体の分子量および分子量分布も種々のものが使用可能であるが、分子量としては、０．５ｇ／ｄｌクロロフォルム溶液、３０℃における還元粘度が０．２０〜０．７０ｄｌ／ｇの範囲が好ましく、０．３０〜０．５５ｄｌ／ｇの範囲がより好ましい。
【００９９】
また、ＰＰＥ重合体中には、本発明の主旨に反しない限り、従来ポリフェニレンエーテル樹脂中に存在させてもよいことが提案されている他の種々のフェニレンエーテルユニットを部分構造として含んでいても構わない。少量共存させることが提案されているものの例としては、特願昭６３−１２６９８号公報および特開昭６３−３０１２２２号公報に記載されている、２−（ジアルキルアミノメチル）−６−メチルフェニレンエーテルユニットや、２−（Ｎ−アルキル−Ｎ−フェニルアミノメチル）−６−メチルフェニレンエーテルユニット等が挙げられる。また、ＰＰＥ重合体の主鎖中にジフェノキノン等が少量結合したものも含まれる。
【０１００】
本発明のＰＰＥ樹脂組成物において、Ｐ成分以外の樹脂成分としてポリスチレン樹脂（Ｓ成分）が使用される。ポリスチレン樹脂（Ｓ成分）としては、それを構成するモノマー単位としてスチレンが８５重量％以上、好ましくは９０重量％以上含有されるものが適当であり、通常ポリスチレン樹脂と称されるものが使用される。例えばＨＩＰＳ（耐衝撃性ポリスチレン）も好適に使用される。
【０１０１】
本発明のＰＰＥ樹脂組成物では、樹脂成分としてのＰ成分およびＳ成分の他に、無機充填材（Ｃ成分）、有機リン化合物系難燃剤（Ｄ成分）および任意成分として含フッ素滴下防止剤（Ｅ成分）が配合される。これらＣ成分、Ｄ成分およびＥ成分の具体的化合物は、前記した樹脂組成物と同じものが使用されるので、ＰＰＥ樹脂組成物では説明を省略する。Ｃ成分、Ｄ成分およびＥ成分は、前記した化合物が使用され、好ましいものとして記載したものが同様に好ましい化合物である。
【０１０２】
本発明のＰＰＥ樹脂組成物における各成分の割合について以下説明する。
樹脂成分であるポリフェニレンエーテル樹脂（Ｐ成分）およびポリスチレン樹脂（Ｓ成分）の合計量は、Ｐ、Ｓ、ＣおよびＤ成分の合計１００重量％当り、５０重量％以上、好ましくは６０重量％以上であり、Ｐ成分およびＳ成分の合計量の上限は、Ｃ成分およびＤ成分の割合により変わるが、８２重量％、好ましくは７５重量％が適当である。Ｐ成分およびＳ成分の両者の割合は、Ｐ成分およびＳ成分の合計１００重量部当り、Ｐ成分５０〜８５重量部でありかつＳ成分１５〜５０重量部であり、好ましくはＰ成分５５〜７５重量部でありかつＳ成分２５〜４５重量部である。
【０１０３】
無機充填材（Ｃ成分）の割合は、Ｃ−１成分およびＣ−２成分の合計として、Ｐ、Ｓ、ＣおよびＤ成分の合計１００重量％当り、１５〜３５重量％、好ましくは２０〜３０重量％である。またＰ、Ｓ、ＣおよびＤ成分の合計１００重量％当り、Ｃ−１成分は１０〜２５重量％、好ましくは１０〜２０重量％、特に好ましくは１２〜２０重量％であり、Ｃ−２成分は３〜１５重量％、好ましくは５〜１５重量％、特に好ましくは５〜１２重量％である。Ｃ−１成分とＣ−２成分との両者の割合は、Ｃ−１成分とＣ−２成分の合計１００重量部当り、Ｃ−１成分が４０〜９０重量部でありかつＣ−２成分が６０〜１０重量部であり、好ましくはＣ−１成分が５０〜８０重量部でありかつＣ−２成分が５０〜２０重量部である。
【０１０４】
難燃剤としての有機リン化合物（Ｄ成分）は、Ｐ、Ｓ、ＣおよびＤ成分の合計１００重量％当り、３〜１５重量％、好ましくは５〜１２重量％である。
【０１０５】
含フッ素滴下防止剤（Ｅ成分）は、Ｐ、ＳおよびＤ成分１００重量部当り、２重量部以下、好ましくは０．０５〜２重量部、特に好ましくは０．１〜１重量部である。また離型剤としての高級脂肪酸エステル（Ｆ成分）を使用することができる。その量はＰ、Ｓ、ＣおよびＤ成分の合計１００重量部当り、２重量部以下、好ましくは０．０１〜２重量部、特に好ましくは０．０５〜１重量部である。
【０１０６】
本発明の難燃性樹脂組成物（ＰＰＥ樹脂組成物も含む）は、上記各成分を同時に、または任意の順序でタンブラー、Ｖ型ブレンダー、ナウターミキサー、バンバリーミキサー、混練ロール、押出機等の混合機により混合して製造することができる。好ましくは２軸押出機による溶融混練が好ましく、さらにその際、Ｃ成分はサイドフィーダー等により第２供給口より、溶融混合された他の成分中に供給することが好ましい。かくして得られた組成物は、射出成形、押出成形、圧縮成形、または回転成形等の既知の方法で容易に成形することができ、特に射出成形により精密機器等の高精度シャーシを成形することが可能である。その際さらに高精度を達成するため、射出圧縮成形、断熱金型による成形等を組合わせることが可能であり、また軽量化および低歪み化のためガスアシスト成形等を組合わせて使用することも可能である。
【０１０７】
以上本発明によれば、剛性、寸法精度、強度に優れ、かつ低金型摩耗性を有する、難燃性樹脂組成物が提供される。さらにこれにより上記樹脂組成物より形成されたシャーシやフレーム成形品が提供される。本発明の難燃性熱可塑性樹脂組成物は光学ユニットなどの精密な機構部品が搭載されるＯＡ関連機器のシャーシやフレームに特に好適である。ＯＡ関連機器としては、プリンター（殊にレーザービーム方式のもの）、複写機、ファクシミリ、およびプロジェクター装置などを挙げることができる。他に精密なセンサーを搭載する家庭用ロボットなどのシャーシやフレームに好適なものである。
【０１０８】
【実施例】
以下に実施例をあげて本発明をさらに説明する。
【０１０９】
［実施例１〜１１および比較例１〜６］
表１〜表６に記載成分のうち、無機充填材（Ｃ−１成分、Ｃ−２成分および本発明以外の無機充填材）を除いた成分であるＡ成分、Ｂ成分、Ｄ成分、Ｐ成分、Ｓ成分およびその他の成分をＶ型ブレンダーにて混合して混合物を作成した。なお、Ｅ成分は、その含有率が２．５重量％となるＡ成分（ＰＣ）またはＰ成分（ＰＰＥ）との予備混合物を、これらをポリエチレン袋中に入れ手動で撹拌することにより作成した後、他の成分と混合した。スクリュー径３０ｍｍのベント式二軸押出機（（株）日本製鋼所ＴＥＸ−３０ＸＳＳＴ）を用いて、Ｖ型ブレンダーにて混合した混合物を最後部の第１投入口より（ただし実施例４および１１のＤ成分は８０℃に加温し定量液体移送装置にて押出機内に所定割合を配合した）、また無機充填材（Ｃ−１成分、Ｃ−２成分および本発明以外の無機充填材）をシリンダー途中の第２供給口よりサイドフィーダーを用いて、計量器を用いて所定の割合となるように供給し、真空ポンプを使用し３ｋＰａの真空下において、シリンダー温度２７０℃で溶融押出ししてペレット化した。得られたペレットを１００℃で６時間、熱風循環式乾燥機にて乾燥し、下記評価項目の説明において特に記載がない限りは、射出成形機（住友重機械工業（株）製 ＳＧ−１５０Ｕ）によりシリンダー温度２６０℃、金型温度７０℃で評価用の試験片を作成し、下記の評価方法で評価を行った。
（１）難燃性樹脂組成物の機械的特性
（ｉ） 剛性 ：ＡＳＴＭ Ｄ−７９０に従って曲げ弾性率を測定した（試験片寸法：長さ１２７ｍｍ×幅１２．７ｍｍ×厚み６．４ｍｍ）。
（ii） 耐衝撃性 ：ＡＳＴＭ Ｄ−２５６に従ってアイゾットノッチ付きインパクトを測定した（Ａ法：試験片厚み３．２ｍｍ）。
（iii） 真密度 ：ＡＳＴＭ Ｄ−７９２（２３℃）に従って測定した。
（ｉｖ） 耐熱性 ：ＡＳＴＭ Ｄ−６４８に従って１．８２ＭＰａ荷重にて荷重たわみ温度を測定した（試験片寸法：長さ１２７ｍｍ×幅１２．７ｍｍ×厚み６．４ｍｍ）。
（ｖ） 燃焼性 ：ＵＬ規格９４Ｖに従い燃焼試験を実施した。
（vi） 成形収縮率：幅５０ｍｍ×長さ１００ｍｍ×厚み４ｍｍの角板を同一の条件で射出成形により成形し２３℃、相対湿度５０％雰囲気にて２４時間放置した後、角板寸法を３次元測定機（ミツトヨ（株）製）により測定し、成形収縮率を算出した。なお、上記角板は、幅５０ｍｍおよび厚み１．５ｍｍのフィルムゲートを長さ方向の一端に有する金型キャビティを用いて成形されたものである。したがって長さ方向が流れ方向、および幅方向が流れ方向と直角の方向となる。さらに角板の成形条件は次のとおりである。すなわち、射出成形機：住友重機械工業（株）製ＳＧ−１５０Ｕ、シリンダー温度：２６０℃、金型温度：７０℃、充填時間：０．７秒、保圧：６１．６ＭＰａ、保圧時間：１５秒、冷却時間：２３秒であった。かかる条件によって良好な成形品が得られた。さらに寸法評価用の角板は、１５ショットを上記条件により連続成形した後、１０ショットを連続して成形し、該成形品の中から５つのサンプルを任意に抽出した。かかるサンプルの平均値を成形収縮率とした。
（vii） 金型摩耗性の評価：図１に示す成形品を２，０００ショット成形し、成形前後のピン（材質アルミニウム）の重量を測定し、その重量減少程度を調べた。測定はピンをヘキサンで洗浄した後１００℃で３時間熱風乾燥機により乾燥し、デシケータ中で１時間放冷した後電子天秤により重量を測定した。金型に組込む際にはキャビティ表面に露出する部分を除いて潤滑油を塗布し、成形試験後は上記と同様に再度ヘキサン洗浄、乾燥、および放冷した後重量を測定した。評価は以下のように行った。
◎：重量減少が０．０５ｍｇ以下
○：重量減少が０．０５ｍｇを超え０．１ｍｇ以下
△：重量減少が０．１ｍｇを超え０．２ｍｇ以下
×：重量減少が０．２ｍｇを超える
【０１１０】
（viii） 離型荷重の測定
図３に示すコップ状成形品を突き出しピンを突き出して離型させる際の離型力を測定した。測定に供された金型の概要を図４に示す。かかる離型力の測定は、突き出し用のプレートにロードセル（９８００Ｎ）を設置しかかるロードセルの先端部が突き出しピンの根元に接して突き出しピンを押し出す構成とすることにより行われた。かかる構成により突き出し時のロードセルにかかる力が測定され、その力の最大値を離型力とした。かかるコップ状成形品を連続して４０ショット成形し離型力を安定化させた後、連続２０ショットの成形を行って各ショットの離型力を測定し、その平均値を表１〜表５中の離型力とした。コップ状成形品の成形条件は次のとおりである。すなわち、射出成形機：ＦＡＮＵＣ製 Ｔ−ｓｅｒｉｅｓ Ｍｏｄｅｌ １５０Ｄ、シリンダー温度２６０℃、金型温度：７０℃、充填時間２．５秒、保圧５８．８ＭＰａ、保圧時間：５秒、冷却時間：２５秒であった。かかる条件によって良好な成形品が得られた。
（ix） 低粘度潤滑油耐性の評価
ＡＳＴＭ規格Ｄ−６３８に従って作成した厚さ３．２ｍｍの試験片（引張りダンベルＴＹＰＥ−Ｉ）に０．５％の曲げ歪みを与え低粘度潤滑油（呉工業（株）製ＣＲＣ５−５６：４０℃の動粘度４．２ｍｍ²／ｓ）を塗布し、８０℃にて７２時間処理した後、成形品外観のクラックの有無を目視観察し、以下の基準で耐薬品性を判定した。試験片の取り付けの概要を図５に示す。
○：クラックの発生無し、×：クラック発生あり。
【０１１１】
なお、曲げ歪み（ε＝０．００５）は３点の内の両端の２点のスパンをＬ（１００ｍｍ）、試験片の厚みをｈ（３．２ｍｍ）、および試験片を水平状態から持ち上げた高さをｙ（ｍｍ）としたとき、ε＝（６ｈｙ）／Ｌ²の式より算出される値である。
【０１１２】
（２）難燃性熱可塑性樹脂組成物の組成成分
なお、表１〜表６に記載の各成分を示す記号は下記の通りである。
（Ａ成分）
ＰＣ−１：芳香族ポリカーボネート樹脂（ビスフェノールＡとホスゲンから常法によって作られた粘度平均分子量２２，５００の芳香族ポリカーボネート樹脂粉末、帝人化成（株）製「パンライトＬ−１２２５ＷＰ」）
ＰＣ−２：芳香族ポリカーボネート樹脂（ビスフェノールＡとホスゲンから常法によって作られた粘度平均分子量１９，７００の芳香族ポリカーボネート樹脂粉末、帝人化成（株）製「パンライトＬ−１２２５ＷＸ」）
（Ｐ成分）
ＰＰＥ：ポリフェニレンエーテル樹脂（ＧＥＭ社製「ＰＰＥ」）
（Ｂ成分）
ＡＳ−１：アクリロニトリル−スチレン共重合体（第一毛織（株）製「ＨＦ５６７０」、ＧＰＣ測定による標準ポリスチレン換算の重量平均分子量：９５，０００、アクリロニトリル含有量：２８．５重量％、スチレン含有量：７１．５重量％）
ＡＳ−２：アクリロニトリル−スチレン共重合体（日本エイアンドエル（株）「ＢＳ−２１８」、ＧＰＣ測定による標準ポリスチレン換算の重量平均分子量：７８，０００、アクリロニトリル含有量：２６重量％、スチレン含有量：７４重量％）
（Ｓ成分）
ＨＩＰＳ：ポリスチレン樹脂（電気化学工業（株）製「デンカスチロールＧＰ−１」）
（Ｃ−１成分）
ＭＩＣＡ−１：平均粒子径約２５０μｍのマスコバイト（燕西鉱業製「ＷＨＩＴＥ ＭＩＣＡ ＰＯＷＤＥＲ ６０ｍｅｓｈ」、モース硬度：３）
ＭＩＣＡ−２：平均粒子径約６０μｍのマスコバイト（燕西鉱業製「ＷＨＩＴＥＭＩＣＡ ＰＯＷＤＥＲ ２５０ｍｅｓｈ」、モース硬度：３）
ＭＩＣＡ−３：平均粒子径約４０μｍマスコバイト（（株）クラレ製「クラライトマイカ３００Ｄ、モース硬度：３）
ＭＩＣＡ−４：平均粒子径約４０μｍマスコバイト（林化成（株）製「ＭＣ−２５０モース硬度：３）
（Ｃ−２成分）
ＴＡＬＣ−１：タルク（勝光山鉱業所（株）製「ビクトリライト タルクＲ」、積重率５０％粒子径：８．５μｍ、ＪＩＳ Ｍ８０１６に従って測定されたハンター白色度：８３．８％、ｐＨ：９．６、およびモース硬度：１）
ＴＡＬＣ−２：タルク（勝光山鉱業所（株）「ビクトリライト ＳＧ−Ａ」、積重率５０％粒子径：１５．２μｍ、ＪＩＳ Ｍ８０１６に従って測定されたハンター白色度：９０．２％、ｐＨ：９．８、およびモース硬度：１）
ＷＳＮ：ワラストナイト（川鉄鉱業（株）「ＰＨ−４５０」、数平均繊維径：１．６μｍ、数平均繊維長：６．７μｍ、モース硬度：４．５］）
（本発明以外の無機充填材）
ＭＩＣＡ−５：マスコバイト（山口雲母（株）「Ａ−４１」平均粒子径約２０μｍ）
ＧＦＬ：顆粒状ガラスフレーク（日本板硝子（株）製フレカＲＥＦＧ−３０１、標準篩法によるメジアン平均径１４０μｍ、厚み５μ、モース硬度：６．５）
（Ｄ成分）
ＦＲ−１：レゾルシノールビス（ジキシレニルホスフェート）（旭電化工業（株）製「アデカスタブＦＰ−５００」、ＴＧＡ５％重量減少温度＝３５１．０℃）ＦＲ−２：ビスフェノールＡビス（ジフェニルホスフェート）を主体とするリン酸エステル（大八化学工業（株）製「ＣＲ−７４１」、ＴＧＡ５％重量減少温度＝３３５．９℃）
ＦＲ−３：トリフェニルホスフェート（大八化学工業（株）製「ＴＰＰ」、ＴＧＡ５％重量減少温度＝２３９．４℃）
（Ｅ成分）
ＰＴＦＥ：フィブリル形成能を有するポリテトラフルオロエチレン（ダイキン工業（株）製「ポリフロンＭＰＡ ＦＡ５００」）
（Ｆ成分）
ＷＡＸ−１：モンタン酸エステル（クラリアントジャパン（株）製「ＷＡＸ−Ｅパウダー」）
（その他の成分）
ＷＡＸ−２：酸変性ポリオレフィン系ワックス（三菱化成（株）ダイヤカルナ３０Ｍ）
ＣＢ：カーボンブラックマスター（越谷化成（株）カーボンブラック４０％含有ポリスチレン樹脂マスター）
【０１１３】
【表１】

【０１１４】
【表２】

【０１１５】
【表３】

【０１１６】
【表４】

【０１１７】
【表５】

【０１１８】
【表６】

【０１１９】
上記表から明らかなように、本発明の難燃性熱可塑性樹脂組成物は高剛性、高強度、高寸法精度、および良好な難燃性を有し、かつ金型を摩耗させにくい特性を有することがわかる。
【０１２０】
更に前記実施例のうち実施例１および２においては、その表面粗さ測定を行った。これらの乾燥後のペレットから長さ１５０ｍｍ×幅１５０ｍｍ×厚さ２ｍｍの平板状試験片（ゲートは辺の一端より幅４０ｍｍ×厚み１ｍｍのフィンゲート）を射出成形により作成し、その表面粗さを測定した。平板状試験片の成形条件は、射出成形機：住友重機械工業（株）製ＳＧ−１５０Ｕ、シリンダ温度：２６０℃、金型温度：５０℃（チラーユニットにより２０℃の冷媒を通してかかる温度を維持）、充填時間：６秒、保圧：７５ＭＰａ、保圧時間：３秒、および冷却時間：２０秒とした。かかる平板状試験片は（株）東京精密製表面粗さ計サーフコム１４００Ａを使用し、その表面粗さが測定され、その結果、実施例１においてはＲａ：２．３μｍおよびＲｙ：１９．１μｍであり、一方実施例２においてはＲａ：１．２μｍおよびＲｙ：８．２μｍであり、実施例２のより小粒径のマイカにおいて極めて良好であった。ここでＲａは算術平均粗さを表し、Ｒｙは最大高さを表す。また測定はＪＩＳ Ｂ０６０１に準拠して行った。
【０１２１】
また上記実施例１〜１１の樹脂組成物においてはいずれも光記録媒体ドライブのシャーシ成形品を成形し、良好なシャーシ成形品がえられた。
【０１２２】
【発明の効果】
本発明の難燃性樹脂組成物は、衝撃強度等の機械的特性、難燃性、寸法安定性、を必要とするあらゆる材料に利用可能である。特に光学ユニットシャーシであるレーザービーム式プリンター光学シャーシおよびレーザービーム式プリンターの構造体フレームなど高い寸法精度を要求されるＯＡ機器分野に有効である。また、本発明の難燃性樹脂組成物は、成形機のスクリューおよび金型摩耗なども少なく成形加工における経済効果も高い。よってその奏する工業的効果は格別なものである。
【図面の簡単な説明】
【図１】［１−Ａ］は、実施例において使用した、金型摩耗評価用の板状成形品の形状を示す正面図である。ゲート近傍に配置されたピン部分は円錐状の凹部を形成する。［１−Ｂ］は、実施例において使用した、金型摩耗評価用の板状成形品の形状を示す側面図である。［１−Ｃ］は、実施例において使用した、金型摩耗評価用の板状成形品の形状を示す底面図である。
【図２】実施例において使用した、金型摩耗評価用のピンの形状を示す正面図である。先端の円錐部分が金型キャビティ表面に露出し溶融樹脂と接触する。
【図３】［３−Ａ］は、実施例において使用した、離型力評価用のコップ状成形品の形状を示す正面図である。［３−Ｂ］は、実施例において使用した、離型力評価用のコップ状成形品の形状を示す側面図図である。［３−Ｃ］は、離型力評価用のコップ状成形品の形状を示す底面図である。
【図４】［４−Ａ］は、離型力評価において用いた金型構造の概略を示す。金型キャビティ内に樹脂が充填された状態を示す。［４−Ｂ］は、上記［４−Ａ］の充填後、冷却されて型開きした状態を示す。この時点では、成形品は可動側金型に密着した状態にある。［４−Ｃ］は、上記［４−Ｂ］の型開き後、突き出しロッドの前進によって、突き出しピンを押し出し、成形品を離型させる。突き出し時の力を突き出しピンと接するロードセルによって検知する。
【図５】上記実施例の評価項目の１つである成形品の低粘度潤滑油耐性の評価における３点曲げを行うジグの概要を示した斜視図である。
【符号の説明】
１ 金型摩耗評価用の板状成形品
２ ピンにより形成された円錐状の凹部
３ ゲート（幅４ｍｍ、厚み１．５ｍｍ）
４ 金型摩耗評価用の板状成形品の長さ（１００ｍｍ）
５ ピンのゲート部からの距離（１０ｍｍ）
６ ピンにより形成された円錐状の凹部の径（ピン径）（１０ｍｍ）
７ 中心線（ピン中心は成形品中心線上）
８ ピンにより形成された円錐状の凹部の深さ（ピン高さ）（３ｍｍ）
９ 金型摩耗評価用の板状成形品の厚み（５ｍｍ）
１０ 金型摩耗評価用の板状成形品の幅（５０ｍｍ）
１１ ピン直径（１０ｍｍ）
１２ ピンの円錐部分（金型キャビティ面露出部分）の高さ（３ｍｍ）
２１ コップ状成形品本体
２２ へた部の対称軸（２６）からの距離（１５ｍｍ）
２３ へた部
２４ へた部の高さ（２０ｍｍ）
２５ コップ上面端面（コーナー部Ｒ：２．５ｍｍ）
２６ 対称軸
２７ 内定孔（半径１ｍｍ）
２８ Ｚピン突起（中心軸から外周部まで半径７．５ｍｍ）
２９ コップ内底部（コーナー部Ｒ：５ｍｍ）
３０ へた部厚み（４ｍｍ）
３１ 中心軸（３４）から内底孔（２７）中心軸までの距離（１３ｍｍ）
３２ 中心軸（３４）からコップ底面（３６）外縁部までの距離（２６ｍｍ）
３３ 中心軸（３４）からコップ上面端（２５）外縁部までの距離（３０ｍｍ）
３４ コップ中心軸
３５ スプルー（外半径６ｍｍ、先端部半径３ｍｍ、長さ３９ｍｍ）
３６ コップ底面部
３７ コップ底面部厚み（４ｍｍ）
３８ コップ外周部厚み（２．５ｍｍ、外周部全て同一）
３９ コップ外周壁
４１ 固定側金型
４２ 成形品
４３ 突き出しピン（先端Ｚピン）
４４ ロードセル
５１ 第１の固定棒（直径３．９ｍｍφのステンレス鋼製）
５２ 試験片の中心部分（試験片の描く弧の頭頂部に位置するように設置。かかる部分に潤滑油を含浸させたガーゼを載せる）
５３ 歪負荷用の移動棒（直径３．９ｍｍφのステンレス鋼製）
５４ 歪負荷用のスクリューネジ（台座５７の裏面部に貫通。無負荷の試験片に接触させた位置から該スクリューネジを回しこみ、スクリューピッチに基づいて所定量の歪を試験片に負荷する）
５５ 試験片（ＡＳＴＭ Ｄ６３８ ＴＹＰＥ Ｉに準拠する形状）
５６ 第２の固定棒（直径３．９ｍｍφのステンレス鋼製）
５７ 台座
５８ 第２の固定棒と歪負荷用の移動棒までの水平距離（５０．０ｍｍ）
５９ 第１の固定棒と歪負荷用の移動棒までの水平距離（５０．０ｍｍ）[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a flame retardant aromatic polycarbonate resin composition. More specifically, (i) the resin component is mainly composed of an aromatic polycarbonate resin, and a small proportion of the component is acrylonitrile-styrene copolymer, and (ii) mica (C-1) having a specific particle size as an inorganic filler. And talc and / or wollastonite (C-2) in combination, (iii) an organic phosphorus compound as a flame retardant, and (iv) a fluorine-containing compound as an anti-drip agent. (A) a molded product having high rigidity, high strength and high dimensional accuracy can be obtained, (b) having good flame retardant properties despite being a relatively small amount of flame retardant, (C) The present invention relates to a resin composition having an advantage that the mold is less worn despite containing an inorganic filler. The resin composition of the present invention is a molded part such as a chassis or a frame, and is suitable for molding various parts that require flame retardancy and high dimensional accuracy.
[0002]
[Prior art]
In recent years, for plastic materials used for chassis and frames of devices having optical system units, such as laser beam printers, copiers, and projector devices (hereinafter, these may be simply referred to as “optical unit chassis”). , High rigidity, high strength, high dimensional accuracy (low anisotropy), and good flame retardancy are required. Many proposals have already been made for plastic materials for such chassis. There is still a high demand for low anisotropy in the optical unit chassis. In addition, a device having the above various optical system units has been manufactured for many years, and much know-how has already been accumulated. In the apparatus having the optical system unit in such a situation, new models with higher performance are developed, and so-called general-purpose models are improved with an emphasis on cost reduction. In such a case, the cost required for the mold of the plastic material and the life of the mold may become a problem. That is, a material with less mold wear (hereinafter referred to as “low mold wear”) is required.
[0003]
A number of resin compositions suitable for molded parts such as chassis and frames have been proposed. (I) A resin composition in which an aromatic polycarbonate resin having a specific molecular weight is highly filled with glass fiber or the like is known (see Patent Document 1). (Ii) It is known that a resin composition comprising an aromatic polycarbonate resin having a specific molecular weight, a non-circular cross-section fiber, and a plate-like inorganic filler, and that the resin composition achieves good low warpage (Patent Document) 2). Further, (iii) an optical writing unit fixing chassis formed of a resin composition comprising an aromatic polycarbonate resin and mica having a specific particle diameter and a specific thickness is known (see Patent Document 3). In particular, the invention described in (iii) Patent Document 3 achieves extremely high rigidity, low warpage and twisting based on low anisotropy, and good flame retardancy. That is, it has desirable characteristics necessary for the optical unit chassis. However, it is difficult to say that the composition of the present invention can provide a molded product that satisfies all the requirements of high rigidity, high strength, low anisotropy (high dimensional accuracy), flame retardancy, and low mold wear. .
[0004]
On the other hand, it is known that a resin composition comprising an aromatic polycarbonate, polycaprolactone, and carbon fiber has reduced mold wear (see Patent Document 4). However, such a resin composition does not sufficiently consider low anisotropy, and Patent Document 4 does not disclose technical knowledge for achieving sufficient strength after achieving low anisotropy.
[0005]
A CD-ROM mechanism component made of a polycarbonate resin, a scaly inorganic filler, and a phosphate compound having a specific structure is known (see Patent Document 5). However, it is difficult to say that Patent Document 5 sufficiently discloses a resin composition that has high rigidity and high strength and that satisfies the requirements of good flame retardancy and low mold wear.
[0006]
A resin composition comprising an aromatic polycarbonate resin, a flame retardant, an inorganic filler in which glass fibers and talc and the like are combined at a specific ratio, and a polytetrafluoroethylene having a fibril forming ability is known (see Patent Document 6). It is known that the composition has high rigidity, high strength, high dimensional accuracy, and good flame retardancy. However, the composition has room for further improvement as a material used in a model in which cost reduction is more important.
[0007]
[Patent Document 1]
Japanese Patent Laid-Open No. 5-287185
[Patent Document 2]
JP-A-6-207189
[Patent Document 3]
JP-A-9-12733
[Patent Document 4]
JP-A-1-185360
[Patent Document 5]
JP-A-8-115589
[Patent Document 6]
JP 2001-164105 A
[0008]
[Problems to be solved by the invention]
The object of the present invention is any of high rigidity, high strength, high dimensional accuracy (low anisotropy), good flame retardancy, and low mold wear, particularly suitable for molded articles for optical unit chassis and frames. The specific object is to provide an aromatic polycarbonate resin composition that satisfies a good balance.
[0009]
As a result of intensive studies to achieve the above object, the present inventor made a resin component by combining an aromatic polycarbonate resin and a specific ratio of acrylonitrile-styrene copolymer (AS resin), and specified particles as inorganic fillers. Resin composition in which talc or wollastonite is used in combination with a specific ratio in diameter mica, an organic phosphorus compound is used as a flame retardant, a fluorine-containing dripping agent is used, and each of these components is blended at a certain ratio It has been found that a molded article that can achieve the object of the present invention can be obtained. That is, when a molded product having high rigidity, high strength, and high dimensional accuracy is obtained, the resin composition exhibits good flame retardancy with a relatively small amount of flame retardant, and the mold wear is extremely low. It has been found that the advantage can be obtained.
[0010]
[Means for Solving the Problems]
According to the present invention,
(A) aromatic polycarbonate resin (component A),
(B) acrylonitrile-styrene copolymer (component B),
(C) inorganic filler (component C),
(D) an organophosphorus compound flame retardant (component D) and
(E) Fluorine-containing anti-dripping agent (E component)
The flame retardant aromatic polycarbonate resin composition is provided, wherein the ratio of each component satisfies the following conditions (i) to (iii).
(I) The total of component A and component B is 50% by weight or more, component C is 15 to 35% by weight, and component D is 3 to 15% by weight per 100% by weight of components A to D In addition, the E component is 0.02 to 2 parts by weight per 100 parts by weight of the total of the A to D components.
(Ii) A component is 75 to 95 parts by weight and B component is 5 to 25 parts by weight per 100 parts by weight of the total of A component and B component.
(Iii) C component is (C1) at least one filler selected from the group consisting of mica (C-1 component) having an average particle size of 30 to 300 μm and (C2) talc and wollastonite (C-2 component) The component C-1 is 10 to 25% by weight, the component C-2 is 3 to 15% by weight and the components C-1 and C-2 per 100% by weight of the components A to D The C-1 component is 40 to 90 parts by weight per 100 parts by weight of the total components.
[0011]
As a result of further research, the present inventor blended a certain proportion of a higher fatty acid ester (F component) of a monohydric or polyhydric alcohol as a mold release agent into the resin composition, and then mixed other types of mold release agents. It has been found that the releasability from the mold is very good as compared with the case.
[0012]
Thus, according to the present invention,
(A) aromatic polycarbonate resin (component A),
(B) acrylonitrile-styrene copolymer (component B),
(C) inorganic filler (component C),
(D) an organophosphorus compound flame retardant (component D) and
(E) Fluorine-containing anti-dripping agent (E component)
(F) Higher fatty acid ester of mono- or polyhydric alcohol (F component)
The flame retardant aromatic polycarbonate resin composition is also provided, wherein the ratio of each component satisfies the following conditions (i) to (iii).
(I) The total of component A and component B is 50% by weight or more, component C is 15 to 35% by weight, and component D is 3 to 15% by weight per 100% by weight of components A to D The E component is 0.02 to 2 parts by weight and the F component is 0.01 to 2 parts by weight per 100 parts by weight of the A to D components.
(Ii) A component is 75 to 95 parts by weight and B component is 5 to 25 parts by weight per 100 parts by weight of the total of A component and B component.
(Iii) C component is (C1) at least one filler selected from the group consisting of mica (C-1 component) having an average particle size of 30 to 300 μm and (C2) talc and wollastonite (C-2 component) The component C-1 is 10 to 20% by weight, the component C-2 is 5 to 15% by weight, and the component C-1 and the component C-2. The C-1 component is 40 to 90 parts by weight per 100 parts by weight of the total components.
[0013]
Next, the resin composition of the present invention will be described in more detail. First, each component constituting the resin composition will be described.
[0014]
In the resin composition of the present invention, the resin component consists essentially of an aromatic polycarbonate resin (component A) and an acrylonitrile-styrene copolymer (component B). The B component acrylonitrile-styrene copolymer is generally referred to as an AS resin.
[0015]
The aromatic polycarbonate resin as the component A can be a known one which has been conventionally used for various molded articles. That is, it is obtained by reacting a dihydric phenol and a carbonate precursor. Examples of the reaction method include an interfacial polycondensation method, a melt transesterification method, a solid phase transesterification method of a carbonate prepolymer, and a ring-opening polymerization method of a cyclic carbonate compound.
[0016]
Representative examples of the dihydric phenol include 2,2-bis (4-hydroxyphenyl) propane (commonly called bisphenol A), 2,2-bis {(4-hydroxy-3-methyl) phenyl} propane, 2, 2-bis (4-hydroxyphenyl) butane, 2,2-bis (4-hydroxyphenyl) -3-methylbutane, 9,9-bis {(4-hydroxy-3-methyl) phenyl} fluorene, 2,2- Bis (4-hydroxyphenyl) -3,3-dimethylbutane, 2,2-bis (4-hydroxyphenyl) -4-methylpentane, 1,1-bis (4-hydroxyphenyl) -3,3,5- And trimethylcyclohexane and α, α′-bis (4-hydroxyphenyl) -m-diisopropylbenzene. In addition, it is possible to copolymerize a divalent aliphatic alcohol such as 1,4-cyclohexanedimethanol. Among the aromatic polycarbonate resins obtained from the above-mentioned various dihydric phenols, a bisphenol A homopolymer can be particularly preferably mentioned. Such an aromatic polycarbonate resin is preferable in terms of excellent impact resistance.
[0017]
As the carbonate precursor, carbonyl halide, carbonate ester, haloformate or the like is used, and specific examples include phosgene, diphenyl carbonate, dihaloformate of dihydric phenol, and the like.
[0018]
In producing an aromatic polycarbonate resin by reacting the above dihydric phenol with a carbonate precursor by an interfacial polycondensation method or a melt transesterification method, a catalyst, a terminal terminator, and a dihydric phenol are oxidized as necessary. You may use antioxidant etc. for preventing this. The aromatic polycarbonate resin may be a branched polycarbonate obtained by copolymerizing a trifunctional or higher polyfunctional aromatic compound. Examples of trifunctional or higher polyfunctional aromatic compounds include 1,1,1-tris (4-hydroxyphenyl) ethane and 1,1,1-tris (3,5-dimethyl-4-hydroxyphenyl) ethane. Can be used.
[0019]
When a polyfunctional compound that produces a branched polycarbonate is included, the ratio is 0.001 to 1 mol%, preferably 0.005 to 0.5 mol%, particularly preferably 0.01 to 0, in the aromatic polycarbonate resin. .3 mol%. In particular, in the case of the melt transesterification method, a branched structure may be generated as a side reaction. The amount of the branched structure is also 0.001 to 1 mol%, preferably 0.005 to 0.005 in the aromatic polycarbonate resin. 5 mol%, particularly preferably 0.01 to 0.3 mol% is preferable. In addition, about this ratio¹It is possible to calculate by H-NMR measurement.
[0020]
Further, it may be a polyester carbonate resin copolymerized with an aromatic or aliphatic bifunctional carboxylic acid. Examples of the aliphatic bifunctional carboxylic acid include aliphatic bifunctional carboxylic acids having 8 to 20 carbon atoms, preferably 10 to 12 carbon atoms. Such aliphatic difunctional carboxylic acid may be linear, branched or cyclic. The aliphatic bifunctional carboxylic acid is preferably α, ω-dicarboxylic acid. Preferred examples of the aliphatic difunctional carboxylic acid include linear saturated aliphatic dicarboxylic acids such as sebacic acid (decanedioic acid), dodecanedioic acid, tetradecanedioic acid, octadecanedioic acid and icosanedioic acid.
[0021]
Further, a polycarbonate-polyorganosiloxane copolymer obtained by copolymerizing polyorganosiloxane units can also be used.
[0022]
The aromatic polycarbonate resin is a mixture of two or more of the above-described various aromatic polycarbonates such as polycarbonates having different dihydric phenols, branched polycarbonates containing branching components, various polyester carbonates, and polycarbonate-polyorganosiloxane copolymers. It may be a thing. Furthermore, what mixed 2 or more types can also be used about various types, such as the aromatic polycarbonate from which a manufacturing method differs below, and the aromatic polycarbonate from which a terminal terminator differs.
[0023]
In the polymerization reaction of an aromatic polycarbonate, the reaction by the interfacial polycondensation method is usually a reaction between a dihydric phenol and phosgene, and is reacted in the presence of an acid binder and an organic solvent. As the acid binder, for example, an alkali metal hydroxide such as sodium hydroxide or potassium hydroxide or an amine compound such as pyridine is used. As the organic solvent, for example, a halogenated hydrocarbon such as methylene chloride or chlorobenzene is used. In order to accelerate the reaction, a catalyst such as a tertiary amine such as triethylamine, tetra-n-butylammonium bromide or tetra-n-butylphosphonium bromide, a quaternary ammonium compound or a quaternary phosphonium compound may be used. it can. At that time, the reaction temperature is usually 0 to 40 ° C., the reaction time is preferably about 10 minutes to 5 hours, and the pH during the reaction is preferably maintained at 9 or more.
[0024]
In such a polymerization reaction, a terminal stopper is usually used. Monofunctional phenols can be used as such end terminators. Specific examples of monofunctional phenols include phenol, p-tert-butylphenol, p-cumylphenol and isooctylphenol. Moreover, you may use a terminal terminator individually or in mixture of 2 or more types.
[0025]
The reaction by the melt transesterification method is usually a transesterification reaction between a dihydric phenol and a carbonate ester, and the alcohol or phenol produced by mixing the dihydric phenol and the carbonate ester with heating in the presence of an inert gas. Is carried out by distilling the water. The reaction temperature varies depending on the boiling point of the alcohol or phenol produced, but is usually in the range of 120 to 350 ° C. In the late stage of the reaction, the reaction system was 1.33 × 10^ThreeDistillation of alcohol or phenol produced by reducing the pressure to about ˜13.3 Pa is facilitated. The reaction time is usually about 1 to 4 hours.
[0026]
Examples of the carbonate ester include esters such as an optionally substituted aryl group having 6 to 10 carbon atoms, an aralkyl group, or an alkyl group having 1 to 4 carbon atoms, and among them, diphenyl carbonate is preferable.
[0027]
Further, a polymerization catalyst can be used to increase the polymerization rate. Examples of the polymerization catalyst include alkali metal compounds such as sodium hydroxide, potassium hydroxide, sodium salt or potassium salt of dihydric phenol; calcium hydroxide, A catalyst such as an alkaline earth metal compound such as barium hydroxide or magnesium hydroxide; a nitrogen-containing basic compound such as tetramethylammonium hydroxide, tetraethylammonium hydroxide, trimethylamine or triethylamine can be used. In addition, alkali (earth) metal alkoxides, alkali (earth) metal organic acid salts, boron compounds, germanium compounds, antimony compounds, titanium compounds or zirconium compounds, etc. The catalyst used for the reaction can be used. A catalyst may be used independently and may be used in combination of 2 or more type. The amount of these polymerization catalysts used is preferably 1 × 10 with respect to 1 mol of dihydric phenol as a raw material.^-8~ 1x10^-3Equivalent weight, more preferably 1 × 10^-7~ 5x10^-FourIt is selected in the range of equivalents.
[0028]
In the reaction by the melt transesterification method, in order to reduce the phenolic end group of the aromatic polycarbonate resin, for example, 2-chlorophenylphenyl carbonate, 2-methoxycarbonylphenylphenyl carbonate, and 2-ethoxy Compounds such as carbonylphenyl phenyl carbonate can be added.
[0029]
Further, in the melt transesterification method, it is preferable to use a deactivator that neutralizes the activity of the catalyst. The amount of the deactivator is preferably 0.5 to 50 mol with respect to 1 mol of the remaining catalyst. Further, it is used in a proportion of 0.01 to 500 ppm, more preferably 0.01 to 300 ppm, particularly preferably 0.01 to 100 ppm with respect to the aromatic polycarbonate resin after polymerization. Preferred examples of the quenching agent include phosphonium salts such as tetrabutylphosphonium salt of dodecylbenzenesulfonic acid and ammonium salts such as tetraethylammonium dodecylbenzyl sulfate.
[0030]
The viscosity average molecular weight of the aromatic polycarbonate resin is not particularly limited, but is preferably in the range of 15,000 to 50,000 in the present invention. The lower limit of the viscosity average molecular weight is more preferably 16,000 or more, further preferably 17,000 or more, and particularly preferably 18,000 or more. On the other hand, the upper limit of the viscosity average molecular weight is preferably 26,000 or less, and more preferably 25,000 or less. The viscosity average molecular weight is particularly preferable when the aromatic polycarbonate resin is contained in an amount of 50% by weight or more, preferably 70% by weight or more in 100% by weight of the component A. When the viscosity average molecular weight of the aromatic polycarbonate is less than 15,000, impact strength, flame retardancy and the like are likely to be lowered. On the other hand, if it exceeds 50,000, the fluidity is lowered, which is not preferable in the present invention.
[0031]
Further, two or more kinds of aromatic polycarbonates may be mixed. In this case, it is naturally possible to mix a polycarbonate resin having a viscosity average molecular weight outside the above range.
[0032]
A mixture with an aromatic polycarbonate having a viscosity average molecular weight exceeding 50,000 has high entropy elasticity and sufficient melt tension. Therefore, it has preferable characteristics when forming a colored layer. In addition, when used as a component of the base layer, there is a feature that molding defects based on rheological behavior represented by prevention of jetting, gas assist stability, and foaming stability are unlikely to occur.
[0033]
More preferred is a mixture with an aromatic polycarbonate resin having a viscosity average molecular weight of 80,000 or more, and further preferred is a mixture with an aromatic polycarbonate resin having a viscosity average molecular weight of 100,000 or more. That is, those capable of observing a molecular weight distribution of two or more peaks in a measuring method such as GPC (gel permeation chromatography) can be preferably used.
[0034]
In the aromatic polycarbonate resin (component A) of the present invention, the amount of phenolic hydroxyl group is preferably 30 eq / ton or less, more preferably 25 eq / ton or less, and further preferably 20 eq / ton or less. Such a value can be substantially 0 eq / ton by sufficiently reacting the terminal terminator. In addition, the amount of the phenolic hydroxyl group is¹H-NMR measurement was performed, and the molar ratio of the divalent phenol unit having a carbonate bond, the divalent phenol unit having a phenolic hydroxyl group, and the terminal terminator unit was calculated, and based on this, the phenolic hydroxyl group amount per polymer weight was calculated. Calculated by conversion.
[0035]
The A component viscosity average molecular weight referred to in the present invention is first determined by using an Ostwald viscometer from a solution in which 0.7 g of an aromatic polycarbonate resin is dissolved in 100 ml of methylene chloride at 20 ° C.
Specific viscosity (η_SP) = (T−t₀) / T₀
[T₀Is the drop time of methylene chloride, t is the drop time of the sample solution]
The obtained specific viscosity is inserted by the following equation to determine the viscosity average molecular weight M.
η_SP/C=[η]+0.45×[η]²c (where [η] is the intrinsic viscosity)
[Η] = 1.23 × 10^-FourM^0.83
c = 0.7
[0036]
In addition, the A component of the present invention is different in dihydric phenol, with or without a terminal terminator, linear and branched, different in production method, Two or more kinds of polycarbonates such as different ones, polycarbonate and polyester carbonate, and those having different viscosity average molecular weights can be mixed.
[0037]
In the resin composition of the present invention, the B component, which is a resin component together with the A component, is an acrylonitrile-styrene copolymer, which is a resin usually called an AS resin. The proportion of each component (monomer) in this B component copolymer (AS resin) is 5 to 50% by weight, preferably 15 to 35% by weight, with respect to 100% by weight of the entire resin. The styrene is 95 to 50% by weight, preferably 85 to 65% by weight. The B component copolymer may be copolymerized with a small proportion of other copolymerizable vinyl compounds in addition to acrylonitrile and styrene. The copolymerization ratio of other vinyl compounds is 15% by weight or less, preferably 10% by weight or less in the component B. As the polymerization initiator or chain transfer agent used for the polymerization reaction of the component B, conventionally known ones can be used as necessary.
[0038]
Such component B (AS resin) may be produced by any of bulk polymerization, solution polymerization, suspension polymerization, and emulsion polymerization, but is preferably bulk polymerization or suspension polymerization. The copolymerization method may be either one-stage copolymerization or multistage copolymerization. Moreover, as for the weight average molecular weight of this B component (AS resin), 40,000-200,000 are preferable in standard polystyrene conversion by GPC measurement. The lower limit is more preferably 50,000, and even more preferably 70,000. The upper limit is more preferably 160,000, further preferably 150,000.
[0039]
In the resin composition of the present invention, the inorganic filler (C component) is characterized by using two types of fillers in combination. One type of inorganic filler (C component) is mica (C-1 component) having a specific average particle size, and the other type is at least one selected from the group consisting of talc and wollastonite (C -2 component).
[0040]
The average particle diameter of mica (C-1 component) in the inorganic filler is a number average particle diameter calculated by a total number of 1,000 indiscriminately observed with a scanning electron microscope. The number average particle diameter is 30 to 300 μm, preferably 30 to 280 μm, more preferably 35 to 260 μm. When the number average particle diameter is less than 30 μm, the impact strength is lowered, and the thermal stability of the aromatic polycarbonate resin may be lowered. On the other hand, if it exceeds 300 μm, the impact strength is improved, but the appearance tends to deteriorate. Deterioration of the appearance deteriorates the slipperiness of a member through which paper passes, and may not be preferable.
[0041]
Even if the average particle diameter of such mica is within the range of the present invention, the more preferable range varies depending on whether the emphasis is on the appearance and the impact strength or rigidity. In the case where the appearance is more important, the number average particle diameter of mica is preferably in the range of 30 to 100 μm, more preferably in the range of 35 to 80 μm. The resin composition of the present invention may be molded under extremely low mold temperature conditions in order to achieve lower cost by shortening the molding time. Therefore, it is appropriate to use mica having a smaller particle size in order to suppress a decrease in slipperiness due to deterioration in appearance. On the other hand, when the appearance is not regarded as important, mica in the range of 100 to 300 μm, more preferably 100 to 260 μm is used from the viewpoint of rigidity and impact strength.
[0042]
As the thickness of mica (C-1 component), a thickness measured by electron microscope observation of 0.01 to 10 μm, preferably 0.1 to 5 μm can be used. An aspect ratio of 5 to 200, preferably 10 to 100 can be used. The mica used (C-1 component) is preferably mascobite mica, and its Mohs hardness is about 3. Muscovite mica can achieve higher rigidity and strength than other mica such as phlogopite, and solves the problems of the present invention at a better level.
[0043]
In addition, as a method for pulverizing mica, a dry pulverization method of pulverizing raw mica ore with a dry pulverizer, and coarsely pulverizing mica rough ore with a dry pulverizer, followed by adding a grinding aid such as water in a slurry state There is a wet pulverization method in which main pulverization is performed by a wet pulverizer, followed by dehydration and drying. The mica of the present invention can be produced by any pulverization method, but the dry pulverization method is generally lower in cost. On the other hand, the wet pulverization method is effective for pulverizing mica more thinly and finely, but is expensive. Mica may be surface-treated with various surface treatment agents such as silane coupling agents, higher fatty acid esters, and waxes, and further granulated with sizing agents such as various resins, higher fatty acid esters, and waxes to form granules. May be.
[0044]
The C-2 component used in combination with the mica (C-1 component) as an inorganic filler is talc and / or wollastonite. The talc used as the C-2 component is a scaly particle having a layered structure, which is a hydrous magnesium silicate in terms of chemical composition.₂・ 3MgO ・ 2H₂Represented by O, usually SiO₂56-65 wt%, MgO 28-35 wt%, H₂O is composed of about 5% by weight. Fe as other minor components₂O_Three0.03 to 1.2% by weight, Al₂O_Three0.05 to 1.5% by weight, CaO 0.05 to 1.2% by weight, K₂O is 0.2 wt% or less, Na₂O contains 0.2% by weight or less, the specific gravity is about 2.7, and the Mohs hardness is 1. In this invention, the flame retardant resin composition which has favorable flame retardance is obtained by using talc (C-2 component) together with mica (C-1 component) of said specific particle diameter. Thus, it has not been conventionally known that a good flame-retardant resin composition can be achieved by using mica and talc having a specific particle size, which are the same plate-like inorganic filler, in combination.
[0045]
The average particle diameter of talc is preferably 0.5 to 30 μm. The average particle size is a particle size at a 50% stacking rate obtained from the particle size distribution measured by the Andreazen pipette method measured according to JIS M8016. The particle diameter of talc is preferably 2 to 30 μm, more preferably 5 to 20 μm, and particularly preferably 10 to 20 μm. Good flame retardancy is achieved in the range of 0.5 to 30 μm.
[0046]
In addition, there is no particular restriction on the manufacturing method when talc is crushed from raw stone, and the axial flow mill method, the annular mill method, the roll mill method, the ball mill method, the jet mill method, the container rotary compression shearing mill method, etc. are used. can do. Further, the talc after pulverization is preferably classified by various classifiers and having a uniform particle size distribution. There are no particular restrictions on the classifier, impactor type inertial force classifier (variable impactor, etc.), Coanda effect type inertial force classifier (elbow jet, etc.), centrifugal field classifier (multistage cyclone, microplex, dispersion separator) , Accucut, Turbo Classifier, Turboplex, Micron Separator, and Super Separator).
[0047]
Further, talc is preferably in an agglomerated state in view of its handleability and the like, and as such a production method, there are a method by deaeration compression, a method of compression using a sizing agent, and the like. In particular, the degassing compression method is preferable in that the sizing agent resin component which is simple and unnecessary is not mixed into the resin composition of the present invention.
[0048]
In addition, wollastonite, which is another C-2 component, substantially has the chemical formula CaSiO._ThreeUsually represented by SiO₂About 50 wt% or more, CaO about 47 wt%, other Fe₂O_Three, Al₂O_ThreeEtc. Wollastonite is a white acicular powder obtained by crushing and classifying raw wollastonite, and has a Mohs hardness of about 4.5. The average fiber diameter of the wollastonite used is preferably 0.5 to 10 μm, and more preferably 1 to 5 μm. The average fiber diameter is calculated by a number average of a total of 1,000 pieces observed with a scanning electron microscope and extracted indiscriminately.
[0049]
Among the above C-2 components, talc is more preferable because it is superior in low mold wear. That is, the inorganic filler (C component) is preferably a combination of mica (C-1 component) and talc (C-2 component), and the ratio of the C-1 component to the C-2 component will be described later. To do.
[0050]
The resin composition of the present invention contains an organic phosphorus compound-based flame retardant (component D) as a flame retardant. By using an organic phosphorus compound-based flame retardant (component D), not only good flame retardancy of a molded product can be achieved by a relatively small blending ratio, but also rigidity (flexural modulus) can be improved, Further, the specific gravity can be reduced as compared with the halogen-based flame retardant. In addition, the low melt viscosity of the resin composition based on the plasticizing effect also has the effect of reducing wear on the mold surface.
[0051]
Examples of the organic phosphorus compound-based flame retardant of component D of the present invention include one or more phosphate esters represented by the following general formula (1).
[0052]
[Chemical 1]

[0053]
(However, X in the above formula is hydroquinone, resorcinol, bis (4-hydroxydiphenyl) methane, bisphenol A, dihydroxydiphenyl, dihydroxynaphthalene, bis (4-hydroxyphenyl) sulfone, bis (4-hydroxyphenyl) ketone, bis And divalent groups derived from (4-hydroxyphenyl) sulfide, j, k, l and m are each independently 0 or 1, n is an integer of 0 to 5, or n number In the case of a mixture of different phosphate esters, the average value is from 0 to 5, and R¹, R², R^Three, And R^FourAre each independently a monovalent group derived from phenol, cresol, xylenol, isopropylphenol, butylphenol or p-cumylphenol substituted or unsubstituted with one or more halogen atoms. )
More preferable examples include a divalent group in which X in the above formula is derived from hydroquinone, resorcinol, bisphenol A, and dihydroxydiphenyl, j, k, l, and m are each 1, and n is An integer of 1 to 3, or an average value in the case of blends of phosphate esters having different numbers of n, and R¹, R², R^Three, And R^FourAre each independently a monovalent group derived from phenol, cresol or xylenol which is substituted or more preferably substituted with one or more halogen atoms.
[0054]
The D component organophosphorus compound has a 5% weight loss temperature of 280 ° C. or higher when the temperature is raised from 23 ° C. in a nitrogen gas atmosphere to 600 ° C. at a rate of temperature increase of 20 ° C./min. Those are preferred. The weight reduction temperature is more preferably 320 ° C. or higher, further preferably 330 ° C. or higher, particularly preferably 340 ° C. or higher. The upper limit of the weight reduction temperature is generally 380 ° C. or lower and is generally available, and 370 ° C. or lower is more appropriate. As described above, the organophosphorus compound having a relatively high weight reduction temperature is preferable in that it can impart good heat resistance (such as good deflection temperature) to the resin composition as well as the effect of lowering the melt viscosity of the resin composition.
[0055]
In consideration of the above points, among the phosphate esters of the above formula, a phosphate ester oligomer mainly composed of resorcinol bis (dixylenyl phosphate), mainly composed of 4,4-dihydroxydiphenylbis (dixylenyl phosphate) Phosphoric acid ester oligomers and phosphoric acid ester oligomers mainly composed of bisphenol A bis (diphenyl phosphate) are preferred (in this case, the main component means that a small amount of other components having different degrees of polymerization may be included). .
[0056]
The resin composition of the present invention contains a fluorine-containing anti-dripping agent (E component). By including this fluorine-containing anti-dripping agent (E component), good flame retardancy can be achieved without impairing the physical properties of the molded product.
[0057]
Examples of the fluorine-containing anti-dripping agent as the E component include a fluorine-containing polymer having a fibril-forming ability. Examples of such a polymer include polytetrafluoroethylene and tetrafluoroethylene-based copolymers (for example, tetrafluoroethylene / hexa Fluoropropylene copolymer, etc.), partially fluorinated polymers as disclosed in US Pat. No. 4,379,910, polycarbonate resins produced from fluorinated diphenols, and the like. Among them, polytetrafluoroethylene (hereinafter sometimes referred to as PTFE) is preferable.
[0058]
PTFE having a fibril forming ability has a very high molecular weight, and tends to be bonded to each other by an external action such as shearing force to form a fiber. The molecular weight is 1 million to 10 million, more preferably 2 million to 9 million in the number average molecular weight determined from the standard specific gravity. Such PTFE can be used in solid form or in the form of an aqueous dispersion. In addition, PTFE having such fibril forming ability can improve the dispersibility in the resin, and it is also possible to use a PTFE mixture in a mixed form with other resins in order to obtain better flame retardancy and mechanical properties. is there.
[0059]
Examples of commercially available PTFE having such fibril forming ability include Teflon 6J from Mitsui DuPont Fluorochemical Co., Ltd., Polyflon MPA FA500 and F-201L from Daikin Industries, Ltd. Commercially available aqueous dispersions of PTFE include Asahi IC Fluoropolymers 'full-on AD-1, AD-936, Daikin Industries' full-on D-1 and D-2, Mitsui Dupont Fluoro A typical example is Teflon 30J manufactured by Chemical Corporation.
[0060]
As a mixed form of PTFE, (1) a method in which an aqueous dispersion of PTFE and an aqueous dispersion or solution of an organic polymer are mixed and co-precipitated to obtain a co-aggregated mixture (Japanese Patent Application Laid-Open No. 60-258263; (Method described in JP-A-63-154744), (2) A method of mixing an aqueous dispersion of PTFE and dried organic polymer particles (method described in JP-A-4-272957), (3) A method in which an aqueous dispersion of PTFE and an organic polymer particle solution are uniformly mixed, and each medium is simultaneously removed from the mixture (described in JP-A-06-220210, JP-A-08-188653, etc.) And (4) a method of polymerizing monomers forming an organic polymer in an aqueous dispersion of PTFE (a method described in JP-A-9-95583), and (5) A method in which an aqueous dispersion of TFE and an organic polymer dispersion are uniformly mixed, and a vinyl monomer is further polymerized in the mixture dispersion, and then a mixture is obtained (described in JP-A-11-29679, etc.). Those obtained by (Method) can be used. Commercially available products of these mixed forms of PTFE include “Metablene A3000” (trade name) manufactured by Mitsubishi Rayon Co., Ltd., and “BLENDEX B449” (trade name) manufactured by GE Specialty Chemicals.
[0061]
As a ratio of PTFE in the mixed form, 1 to 60% by weight of PTFE is preferable in 100% by weight of the PTFE mixture, and more preferably 5 to 55% by weight. When the ratio of PTFE is within such a range, good dispersibility of PTFE can be achieved. In addition, the ratio of the said E component shows the quantity of a net fluorine-containing dripping inhibitor, and in the case of mixed form PTFE, it shows a net PTFE quantity.
[0062]
The resin composition of the present invention preferably further contains an ester (F component) of a monohydric or polyhydric alcohol and a higher fatty acid as an optional component. The use of the F component provides a resin composition having excellent releasability while maintaining the above-described effects of the present invention. As a result, a molded article having better dimensional stability is provided. In particular, when the D component more preferable in the present invention is contained, the preferable effect of the F component is particularly exhibited. The more preferable D component is as described above.
[0063]
The higher fatty acid constituting the ester of the F component preferably contains 60% by weight or more of a fatty acid having 20 or more carbon atoms (more preferably 20 to 32 carbon atoms, more preferably 26 to 32 carbon atoms). As such a higher fatty acid, a higher fatty acid mainly composed of montanic acid is preferably exemplified. Such higher fatty acids are usually produced by oxidizing montan wax.
[0064]
Examples of the monohydric alcohol constituting the F component include dodecanol, tetradecanol, hexadecanol, octadecanol, eicosanol, tetracosanol, seryl alcohol, and triacontanol.
[0065]
Examples of the polyhydric alcohol constituting the F component include ethylene glycol, glycerin, diglycerin, polyglycerin (such as decaglycerin), pentaerythritol, dipentaerythritol, trimethylolpropane, diethylene glycol, and propylene glycol. Among these, ethylene glycol, glycerin, pentaerythritol, dipentaerythritol, and trimethylolpropane are preferable, and ethylene glycol is particularly preferable.
[0066]
Esters of higher fatty acids based on montanic acid and mono- or polyhydric alcohols (preferably polyhydric alcohols) have a density of 0.94 to 1.10 g / cm.^ThreeThe acid value is preferably in the range of 1 to 200 and the saponification value is in the range of 50 to 200, and more preferably the density is 0.98 to 1.06 g / cm.^Three, Acid value: 5-30, saponification value: 100-180.
[0067]
Next, the ratios of the A to E components and the optional F component constituting the resin composition of the present invention will be described.
[0068]
In the resin composition of the present invention, the total amount of aromatic polycarbonate resin (A component) and acrylonitrile-styrene copolymer (B component; AS resin), which are resin components, is the A component, B component, C component, and D component. The total amount is 50% by weight or more, preferably 60% by weight or more. The upper limit of the total amount of the A component and the B component mainly depends on the ratio of the C component and the D component, but is 80% by weight, preferably 76% by weight.
[0069]
The ratio of both the A component and the B component is 75 to 95 parts by weight of the A component and 5 to 25 parts by weight of the B component per 100 parts by weight of the total of the A component and the B component. 92 parts by weight and 8 to 22 parts by weight of B component.
[0070]
The proportion of the inorganic filler (C component) is 15 to 35% by weight, preferably 20 to 30% by weight, based on the total of 100% by weight of components A to D, as the sum of components C-1 and C-2. . Further, the C-1 component is 10 to 25% by weight, preferably 10 to 20% by weight, particularly preferably 12 to 20% by weight, and the C-2 component is 3 to 15% per 100% by weight of the total of the A to D components. % By weight, preferably 5-15% by weight, particularly preferably 5-12% by weight. The ratio of both the C-1 component and the C-2 component is 40 to 90 parts by weight of the C-1 component and 100% by weight of the C-2 component per 100 parts by weight of the total of the C-1 component and the C-2 component. 60 to 10 parts by weight, preferably 50 to 80 parts by weight of the C-1 component and 50 to 20 parts by weight of the C-2 component.
[0071]
The organophosphorus compound (D component) as a flame retardant is 3 to 15% by weight, preferably 3 to 10% by weight, and more preferably 3 to 6% by weight per 100% by weight of the total of the A to D components.
[0072]
The fluorine-containing anti-dripping agent (component E) is 0.02 to 2 parts by weight, preferably 0.05 to 2 parts by weight, more preferably 0.1 to 1 part by weight, based on 100 parts by weight of the components AD. Preferably it is 0.15-0.8 weight part. The higher fatty acid ester (F component) as a release agent is 2 parts by weight or less, preferably 0.01 to 2 parts by weight, more preferably 0.05 to 1 part by weight per 100 parts by weight of the components A to D. 5 parts by weight, particularly preferably 0.1 to 1.0 part by weight.
[0073]
The resin composition of the present invention is a combination of the above-described A to F components and the composition ratio thereof, so that a molded product from the composition has excellent physical properties and excellent flame retardancy. . That is, the impact strength (J / m) of the molded product is 30 or more, preferably 35 or more, and the upper limit is preferably 55. Further, the shrinkage anisotropy of the molded product (absolute value of the difference in molding shrinkage (%) in the direction perpendicular to the flow direction of the molded product) is small and has a value of 0.15 or less, preferably 0.10 or less.
[0074]
The molded product from the resin composition of the present invention has a V-1 level in a flame retardant test of a 1.6 mm-thick test piece according to the UL94 standard, although the flame retardant (component D) content is relatively small. Can be achieved.
[0075]
Moreover, the molded article of this invention provides the resin composition of high rigidity and low specific gravity with the combination of B component, C-1 component and C-2 component of an inorganic filler, and D component. More specifically, the specific gravity is expressed as a true density of 1.3 to 1.45 (g / cm^Three), 1.32-1.40 (g / cm) under suitable conditions^Three).
[0076]
The molded product from the resin composition comprising the A component to the E component and the resin composition comprising the A component to the F component of the present invention has good resistance to the low viscosity lubricating oil. The chassis molded product may be pre-lubricated with lubricant or may be applied during use so that various mechanical parts assembled in the chassis molded product operate smoothly. Thus, such good resistance is a desirable property required for chassis molded articles.
[0077]
Examples of the low-viscosity lubricating oil include hydrocarbon oil, silicone oil, and fluorine oil. The molded product from the resin composition comprising the A component to the E component and the resin composition comprising the A component to the F component of the present invention has good resistance to hydrocarbon oils widely used among these. In particular, it has good resistance to a lubricating oil mainly composed of paraffin oil, which is frequently used.
[0078]
The low viscosity lubricating oil is 2-20 mm at 40 ° C.²Having a kinematic viscosity in the range of / s, more preferably 2 to 10 mm²It has a kinematic viscosity in the range of / s. Specific examples of the low-viscosity lubricating oil include CRC5-56 manufactured by Kure Kogyo Co., Ltd.
[0079]
According to the resin composition of the present invention, due to the use of a combination of the C-1 component and the C-2 component as the inorganic filler (C component), the wearability of the mold is extremely small and the molding cost can be reduced. Has advantages.
[0080]
The resin composition of the present invention may contain other components as long as the ratio of the A to F components described above is maintained and the purpose is not impaired. For example, as thermoplastic resins other than the A component and the B component, for example, polyethylene resin, polypropylene resin, polyalkyl methacrylate resin, polyacetal resin, polyalkylene terephthalate resin, polyamide resin, cyclic polyolefin resin, polyarylate resin (amorphous) And various thermoplastic polyimides represented by polyether ether ketone, polyether imide, polyamide imide, and the like, polysulfone, polyether sulfone, polyphenylene sulfide, and the like. These can be used in combination with the above component A and component B depending on the purpose. In particular, when a polyarylate resin is required to have vibration damping properties, it may be preferable to use the polyarylate resin in combination because it can achieve both good flame retardancy and vibration damping properties.
[0081]
Furthermore, the flame-retardant thermoplastic resin composition of the present invention can contain a small amount of a rubbery polymer. The ratio is suitably 1.5 parts by weight or less, more preferably 1.3 parts by weight or less, still more preferably 1 part by weight or less with respect to 100 parts by weight of the total of the A component to D component. .
[0082]
More specifically, as the rubbery polymer, SB (styrene-butadiene) polymer, ABS (acrylonitrile-butadiene-styrene) polymer, MBS (methyl methacrylate-butadiene-styrene) polymer, MABS (methyl methacrylate-acrylonitrile-) Butadiene-styrene) polymer, MB (methyl methacrylate-butadiene) polymer, ASA (acrylonitrile-styrene-acrylic rubber) polymer, AES (acrylonitrile-ethylenepropylene rubber-styrene) polymer, MA (methyl methacrylate-acrylic rubber) Polymer, MAS (methyl methacrylate-acrylic rubber-styrene) polymer, methyl methacrylate-acrylic butadiene rubber copolymer, methyl methacrylate-acrylic butadiene rubber-styrene copolymer Coalescence, methyl methacrylate - and the like (acrylic silicone IPN rubber) polymer. Any of these polymers is preferably a core-shell type graft copolymer in which a polymer chain composed of the above monomer is bonded to a polymer core composed of a rubber component.
[0083]
The rubbery polymer of the present invention may be in a form contained in other components. Examples of such a rubbery polymer include an ABS copolymer contained in an ABS resin.
[0084]
Examples of the flame retardant other than the organic phosphorus compound of component D in the present invention include a red phosphorus flame retardant, a halogen flame retardant, a silicone flame retardant, and a metal salt flame retardant. However, in the present invention, those containing substantially only the D component as the flame retardant are suitable.
[0085]
The present invention may contain a small amount of an inorganic filler other than the C-1 component and the C-2 component as long as the object of the present invention is not impaired. Here, glass-based fillers such as glass fibers and glass flakes (Mohs hardness of about 6.5), aluminum borate whiskers (Mohs hardness of about 7), and titanium oxide (rutile type of Mohs hardness of about 7) have high hardness. The proportion of the filler is suitably 3 parts by weight or less, more preferably 1 part by weight or less, with respect to the total of 100 parts by weight of the components A to D. On the other hand, if the filler has a Mohs hardness of 5 or less, it can be blended in an amount exceeding 3 parts by weight, but it is preferably 5 parts by weight or less.
[0086]
The resin composition of the present invention includes heat stabilizers, antioxidants, ultraviolet absorbers, mold release agents (other than the F component), antistatic agents, foaming agents, dyes and pigments (especially carbon black, titanium oxide, etc.) ) Etc. can also be blended.
[0087]
Examples of the heat stabilizer include phosphorus-based heat stabilizers such as phosphorous acid, phosphoric acid, phosphonous acid, phosphonic acid, and esters thereof. Specific examples thereof include triphenyl phosphite, trisnonylphenyl phosphite. , Tris (2,4-di-tert-butylphenyl) phosphite, tridecyl phosphite, trioctyl phosphite, trioctadecyl phosphite, didecyl monophenyl phosphite, dioctyl monophenyl phosphite, diisopropyl monophenyl phosphite , Monobutyl diphenyl phosphite, monodecyl diphenyl phosphite, monooctyl diphenyl phosphite, bis (2,6-di-tert-butyl-4-methylphenyl) pentaerythritol diphosphite, 2,2-methylene bis (4 6-di- phosphite compounds such as ert-butylphenyl) octyl phosphite, bis (nonylphenyl) pentaerythritol diphosphite, bis (2,4-di-tert-butylphenyl) pentaerythritol diphosphite, tributyl phosphate, trimethyl Phosphate compounds such as phosphate, tricresyl phosphate, triphenyl phosphate, trichlorophenyl phosphate, triethyl phosphate, diphenyl cresyl phosphate, diphenyl monoorthoxenyl phosphate, tributoxyethyl phosphate, dibutyl phosphate, dioctyl phosphate, diisopropyl phosphate, Furthermore, tetrakis (2,4-di-tert-butylphenyl) -4,4 is another phosphorous heat stabilizer. -Biphenylenediphosphonite, tetrakis (2,4-di-tert-butylphenyl) -4,3'-biphenylenediphosphonite, tetrakis (2,4-di-tert-butylphenyl) -3,3'-biphenyl Examples thereof include phosphonite compounds such as range phosphonite and bis (2,4-di-tert-butylphenyl) -4-biphenylene phosphonite. Among these, trisnonylphenyl phosphite, distearyl pentaerythritol diphosphite, bis (2,4-di-tert-butylphenyl) pentaerythritol diphosphite, tris (2,4-di-tert-butylphenyl) Phosphite, triphenyl phosphate, trimethyl phosphate, tetrakis (2,4-di-tert-butylphenyl) -4,4′-biphenylenediphosphonite, bis (2,4-di-tert-butylphenyl) -4- Biphenylene phosphonite is preferred. These heat stabilizers may be used alone or in admixture of two or more. The blending amount of the heat stabilizer is preferably 0.0001 to 1 part by weight, more preferably 0.0005 to 0.5 part by weight, and more preferably 0.002 to 0 part by weight with respect to 100 parts by weight of the total of A component to D component. More preferred is 3 parts by weight.
[0088]
Examples of the antioxidant include pentaerythritol tetrakis (3-mercaptopropionate), pentaerythritol tetrakis (3-lauryl thiopropionate), glycerol-3-stearyl thiopropionate, triethylene glycol-bis [3- (3-t-butyl-5-methyl-4-hydroxyphenyl) propionate], 1,6-hexanediol-bis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate], penta Erythritol-tetrakis [3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate], octadecyl-3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate, 1,3 , 5-trimethyl-2,4,6-tris (3,5-di-t-butyl 4-hydroxybenzyl) benzene, N, N-hexamethylenebis (3,5-di-t-butyl-4-hydroxy-hydrocinnamide), 3,5-di-t-butyl-4-hydroxy- Benzylphosphonate-diethyl ester, tris (3,5-di-t-butyl-4-hydroxybenzyl) isocyanurate, 4,4′-biphenylenediphosphosphinic acid tetrakis (2,4-di-t-butylphenyl), 3,9-bis {1,1-dimethyl-2- [β- (3-tert-butyl-4-hydroxy-5-methylphenyl) propionyloxy] ethyl} -2,4,8,10-tetraoxaspiro (5,5) Undecane etc. are mentioned. The blending amount of these antioxidants is preferably 0.0001 to 0.05 parts by weight with respect to 100 parts by weight of the total of A component to D component.
[0089]
Examples of the ultraviolet absorber include benzophenone-based ultraviolet absorbers represented by 2,2′-dihydroxy-4-methoxybenzophenone, and, for example, 2- (3-tert-butyl-5-methyl-2-hydroxyphenyl) -5. -Chlorobenzotriazole, 2- (3,5-di-tert-butyl-2-hydroxyphenyl) -5-chlorobenzotriazole, 2,2'-methylenebis [4- (1,1,3,3-tetramethyl Butyl) -6- (2H-benzotriazol-2-yl) phenol], 2- [2-hydroxy-3,5-bis (α, α-dimethylbenzyl) phenyl] -2H-benzotriazole and 2- (3 , 5-Di-tert-amyl-2-hydroxyphenyl) benzotriazole-based UV absorption represented by benzotriazole Agents are exemplified. Further, hindered amine light stabilizers typified by bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, bis (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate and the like Can also be used. As for the compounding quantity of this ultraviolet absorber and light stabilizer, 0.01-5 weight part is preferable with respect to a total of 100 weight part of A component-D component.
[0090]
Examples of the mold release agent other than the component F include olefin wax, silicone oil, fluorine oil, organopolysiloxane, paraffin wax, and beeswax.
[0091]
Examples of the antistatic agent include polyether ester amide, glycerin monostearate, ammonium dodecylbenzenesulfonate, phosphonium dodecylbenzenesulfonate, maleic anhydride monoglyceride, maleic anhydride diglyceride and the like. The blending amount of the antistatic agent is preferably 0.5 to 20 parts by weight with respect to 100 parts by weight as a total of the A component to the D component.
[0092]
As a result of further studies by the present inventor, it has been found that the advantages and effects of the resin composition described above can be similarly achieved in a resin composition in which the resin component is a polyphenylene ether resin and a polystyrene resin.
[0093]
Thus, according to the present invention,
(1) polyphenylene ether resin (P component),
(2) polystyrene resin (S component),
(3) inorganic filler (component C),
(4) organophosphorus compound flame retardant (component D) and
(5) Fluorine-containing anti-dripping agent (E component)
The flame retardant aromatic polyphenylene ether resin composition (hereinafter referred to as “PPE resin composition”) is characterized in that the ratio of these components satisfies the following conditions (i) to (iii): Is done.
(I) The total of P component and S component is 50% by weight or more per 100% by weight of P, S, C and D components, C component is 15 to 35% by weight, and D component is 3 to 15%. E component is 0 to 2 parts by weight per 100 parts by weight of the total of P, S, C and D components,
(Ii) The P component is 50 to 85 parts by weight and the S component is 15 to 50 parts by weight per 100 parts by weight of the total of the P component and the S component.
(Iii) C component is (C1) at least one filler selected from the group consisting of mica (C-1 component) having an average particle size of 30 to 300 μm and (C2) talc and wollastonite (C-2 component) ), The C-1 component is 10 to 25% by weight, the C-2 component is 3 to 15% by weight and the C-1 component per 100% by weight of the total of P, S, C and D components The C-1 component is 40 to 90 parts by weight per 100 parts by weight in total of the C-2 component.
[0094]
The polyphenylene ether resin (P component) in this PPE resin composition is a polymer or copolymer of a nucleus-substituted phenol having a phenylene ether structure (hereinafter sometimes simply referred to as a PPE polymer).
[0095]
Typical examples of the polymer of the nucleus-substituted phenol having a phenylene ether structure include poly (2,6-dimethyl-1,4-phenylene) ether and poly (2-methyl-6-ethyl-1,4-phenylene) ether. Poly (2,6-diethyl-1,4-phenylene) ether, poly (2-ethyl-6-n-propyl-1,4-phenylene) ether, poly (2,6-di-n-propyl-1) , 4-phenylene) ether, poly (2-methyl-6-n-butyl-1,4-phenylene) ether, poly (2-ethyl-6-isopropyl-1,4-phenylene) ether, poly (2-methyl) -6-hydroxyethyl-1,4-phenylene) ether, poly (2-methyl-6-chloroethyl-1,4-phenylene) ether, and the like. Of these, poly (2,6-dimethyl-1,4-phenylene) ether is particularly preferred.
[0096]
Representative examples of the copolymer of a nucleus-substituted phenol having a phenylene ether structure include a copolymer of 2,6-dimethylphenol and 2,3,6-trimethylphenol, 2,6-dimethylphenol and o-cresol, Or a copolymer of 2,6-dimethylphenol with 2,3,6-trimethylphenol and o-cresol.
[0097]
The method for producing the above PPE polymer is not particularly limited. For example, according to the method described in US Pat. No. 4,788,277 (Japanese Patent Application No. 62-77570), in the presence of dibutylamine. In addition, 2,6-xylenol can be produced by oxidative coupling polymerization.
[0098]
Various molecular weights and molecular weight distributions of the PPE polymer can be used. The molecular weight ranges from 0.50 / 0.70 dl / g in 0.5 g / dl chloroform solution at a reduced viscosity at 30 ° C. Is preferable, and the range of 0.30 to 0.55 dl / g is more preferable.
[0099]
In addition, the PPE polymer may include other various phenylene ether units that have been proposed to exist in the polyphenylene ether resin as a partial structure, unless they are contrary to the gist of the present invention. I do not care. Examples of those proposed to coexist in a small amount include 2- (dialkylaminomethyl) -6-methylphenylene ether described in Japanese Patent Application Nos. 63-12698 and 63-301222. Unit, 2- (N-alkyl-N-phenylaminomethyl) -6-methylphenylene ether unit, and the like. Moreover, the thing which a small amount of diphenoquinone etc. couple | bonded in the principal chain of a PPE polymer is also contained.
[0100]
In the PPE resin composition of the present invention, a polystyrene resin (S component) is used as a resin component other than the P component. As the polystyrene resin (S component), those containing 85% by weight or more, preferably 90% by weight or more of styrene as a monomer unit constituting it are suitable, and those usually called polystyrene resins are used. . For example, HIPS (high impact polystyrene) is also preferably used.
[0101]
In the PPE resin composition of the present invention, in addition to the P component and S component as the resin component, an inorganic filler (C component), an organic phosphorus compound-based flame retardant (D component), and a fluorine-containing anti-dripping agent (optional component) E component) is blended. Since the specific compounds of these C component, D component, and E component are the same as those described above, the description thereof is omitted for the PPE resin composition. As the C component, the D component, and the E component, the above-described compounds are used, and those described as preferable are similarly preferable compounds.
[0102]
The ratio of each component in the PPE resin composition of the present invention will be described below.
The total amount of polyphenylene ether resin (P component) and polystyrene resin (S component) as resin components is 50% by weight or more, preferably 60% by weight or more, per 100% by weight of the total of P, S, C and D components. The upper limit of the total amount of the P component and the S component varies depending on the ratio of the C component and the D component, but is 82% by weight, preferably 75% by weight. The proportion of both P component and S component is 50 to 85 parts by weight of P component and 15 to 50 parts by weight of S component, preferably 55 to 75 parts by weight, per 100 parts by weight of P component and S component. Parts by weight and 25 to 45 parts by weight of the S component.
[0103]
The ratio of the inorganic filler (C component) is 15 to 35% by weight, preferably 20 to 30% per 100% by weight of the total of P, S, C and D components as the sum of C-1 component and C-2 component. % By weight. Further, the C-1 component is 10 to 25% by weight, preferably 10 to 20% by weight, particularly preferably 12 to 20% by weight, based on 100% by weight of the total of P, S, C and D components. Is 3 to 15% by weight, preferably 5 to 15% by weight, particularly preferably 5 to 12% by weight. The ratio of both the C-1 component and the C-2 component is 40 to 90 parts by weight of the C-1 component and 100% by weight of the C-2 component per 100 parts by weight of the total of the C-1 component and the C-2 component. 60 to 10 parts by weight, preferably 50 to 80 parts by weight of the C-1 component and 50 to 20 parts by weight of the C-2 component.
[0104]
The organophosphorus compound (D component) as a flame retardant is 3 to 15% by weight, preferably 5 to 12% by weight per 100% by weight of the total of P, S, C and D components.
[0105]
The fluorine-containing anti-dripping agent (E component) is 2 parts by weight or less, preferably 0.05 to 2 parts by weight, particularly preferably 0.1 to 1 part by weight, per 100 parts by weight of the P, S and D components. Moreover, the higher fatty acid ester (F component) as a mold release agent can be used. The amount thereof is 2 parts by weight or less, preferably 0.01 to 2 parts by weight, particularly preferably 0.05 to 1 part by weight per 100 parts by weight of the total of P, S, C and D components.
[0106]
The flame-retardant resin composition (including PPE resin composition) of the present invention is a tumbler, V-type blender, nauter mixer, Banbury mixer, kneading roll, extruder, etc. It can be manufactured by mixing with a mixer. Preferably, melt kneading with a twin-screw extruder is preferred, and at that time, the C component is preferably fed into the other melt-mixed component from the second supply port by a side feeder or the like. The composition thus obtained can be easily molded by a known method such as injection molding, extrusion molding, compression molding, or rotational molding, and in particular, a high-precision chassis such as a precision instrument can be molded by injection molding. Is possible. At that time, in order to achieve higher accuracy, it is possible to combine injection compression molding, molding with a heat insulating mold, etc., and also use gas assist molding etc. in combination for weight reduction and distortion reduction. Is possible.
[0107]
As described above, according to the present invention, there is provided a flame retardant resin composition which is excellent in rigidity, dimensional accuracy and strength, and has low mold wear. Furthermore, this provides a chassis and a frame molded product formed from the resin composition. The flame-retardant thermoplastic resin composition of the present invention is particularly suitable for chassis and frames of OA related equipment on which precise mechanical parts such as optical units are mounted. Examples of the OA-related equipment include a printer (particularly a laser beam type), a copying machine, a facsimile machine, and a projector apparatus. In addition, it is suitable for chassis and frames of home robots and the like equipped with precision sensors.
[0108]
【Example】
The following examples further illustrate the present invention.
[0109]
[Examples 1 to 11 and Comparative Examples 1 to 6]
Among the components listed in Tables 1 to 6, A component, B component, D component, and P component excluding inorganic fillers (C-1 component, C-2 component and inorganic filler other than the present invention) , S component and other components were mixed in a V-type blender to prepare a mixture. In addition, after preparing E component, the preliminary mixture with A component (PC) or P component (PPE) which the content rate will be 2.5 weight% puts these in a polyethylene bag, and is stirred manually. , Mixed with other ingredients. Using a vent type twin screw extruder (Nippon Steel Works TEX-30XSST) with a screw diameter of 30 mm, the mixture mixed in the V-type blender was passed through the first input port at the end (however, in Examples 4 and 11). D component was heated to 80 ° C. and a predetermined ratio was blended in the extruder with a metered liquid transfer device), and inorganic fillers (C-1 component, C-2 component and inorganic fillers other than the present invention) were cylinders Using a side feeder from the second supply port in the middle, supply it to a predetermined ratio using a measuring instrument, and using a vacuum pump under a 3 kPa vacuum, melt extrusion at a cylinder temperature of 270 ° C. and pelletizing did. The obtained pellets were dried with a hot air circulation dryer at 100 ° C. for 6 hours, and unless otherwise specified in the description of the following evaluation items, an injection molding machine (SG-150U, manufactured by Sumitomo Heavy Industries, Ltd.). The test piece for evaluation was created at a cylinder temperature of 260 ° C. and a mold temperature of 70 ° C., and evaluated by the following evaluation method.
(1) Mechanical properties of flame retardant resin composition
(I) Rigidity: The flexural modulus was measured according to ASTM D-790 (test piece dimensions: length 127 mm × width 12.7 mm × thickness 6.4 mm).
(Ii) Impact resistance: Impact with an Izod notch was measured according to ASTM D-256 (Method A: specimen thickness 3.2 mm).
(Iii) True density: Measured according to ASTM D-792 (23 ° C.).
(Iv) Heat resistance: The deflection temperature under a load of 1.82 MPa was measured according to ASTM D-648 (test piece dimensions: length 127 mm × width 12.7 mm × thickness 6.4 mm).
(V) Flammability: A combustion test was performed in accordance with UL standard 94V.
(Vi) Molding shrinkage ratio: A square plate having a width of 50 mm, a length of 100 mm, and a thickness of 4 mm was molded by injection molding under the same conditions and left standing at 23 ° C. and a relative humidity of 50% for 24 hours. It measured with the dimension measuring machine (made by Mitutoyo Co., Ltd.), and calculated the mold shrinkage rate. The square plate is formed using a mold cavity having a film gate having a width of 50 mm and a thickness of 1.5 mm at one end in the length direction. Therefore, the length direction is the flow direction, and the width direction is a direction perpendicular to the flow direction. Further, the molding conditions of the square plate are as follows. That is, injection molding machine: Sumitomo Heavy Industries, Ltd. SG-150U, cylinder temperature: 260 ° C., mold temperature: 70 ° C., filling time: 0.7 seconds, holding pressure: 61.6 MPa, holding pressure time: 15 seconds, cooling time: 23 seconds. Under such conditions, a good molded product was obtained. Further, the square plate for dimensional evaluation was formed by continuously forming 15 shots under the above conditions, then forming 10 shots continuously, and arbitrarily extracting five samples from the molded product. The average value of these samples was taken as the mold shrinkage.
(Vii) Evaluation of mold wearability: The molded product shown in FIG. 1 was molded into 2,000 shots, the weight of the pin (material aluminum) before and after molding was measured, and the degree of weight reduction was examined. The pin was washed with hexane, dried with a hot air dryer at 100 ° C. for 3 hours, allowed to cool in a desiccator for 1 hour, and then weighed with an electronic balance. When incorporated into the mold, the lubricating oil was applied except for the portion exposed on the cavity surface, and after the molding test, hexane was washed again, dried, and allowed to cool as before, and the weight was measured. Evaluation was performed as follows.
A: Weight reduction is 0.05 mg or less
○: Weight reduction exceeds 0.05 mg and 0.1 mg or less
Δ: Weight loss exceeds 0.1 mg and is 0.2 mg or less
X: Weight loss exceeds 0.2 mg
[0110]
(Viii) Release load measurement
The mold release force was measured when the cup-shaped molded product shown in FIG. An outline of the mold used for the measurement is shown in FIG. The release force was measured by setting a load cell (9800N) on a plate for protrusion and pushing the protrusion pin with the tip of the load cell being in contact with the root of the protrusion pin. With this configuration, the force applied to the load cell at the time of ejection was measured, and the maximum value of the force was defined as the mold release force. The cup-shaped molded product was continuously molded into 40 shots to stabilize the mold release force, and then continuously shot into 20 shots to measure the mold release force for each shot. The average values are shown in Tables 1 to 5 below. The middle mold release force. The molding conditions for the cup-shaped molded product are as follows. That is, injection molding machine: T-series Model 150D manufactured by FANUC, cylinder temperature 260 ° C., mold temperature: 70 ° C., filling time 2.5 seconds, holding pressure 58.8 MPa, holding pressure 5 seconds, cooling time 25 Second. Under such conditions, a good molded product was obtained.
(Ix) Evaluation of low-viscosity lubricating oil resistance
A low-viscosity lubricant (CRC5-56 manufactured by Kure Kogyo Co., Ltd .: 40 ° C.) with a bending strain of 0.5% applied to a 3.2 mm thick test piece (tensile dumbbell TYPE-I) prepared in accordance with ASTM standard D-638. Kinematic viscosity of 4.2 mm²/ S) was applied and treated at 80 ° C. for 72 hours, and then the presence or absence of cracks in the appearance of the molded product was visually observed, and the chemical resistance was determined according to the following criteria. An outline of the test piece attachment is shown in FIG.
○: No crack occurred, ×: Crack occurred.
[0111]
In addition, bending strain (ε = 0.005) was obtained by lifting the span of two points at both ends of three points to L (100 mm), the thickness of the test piece to h (3.2 mm), and the test piece from the horizontal state. When the height is y (mm), ε = (6hy) / L²It is a value calculated from the formula of
[0112]
(2) Composition component of flame retardant thermoplastic resin composition
In addition, the symbol which shows each component of Table 1-Table 6 is as follows.
(A component)
PC-1: Aromatic polycarbonate resin (Aromatic polycarbonate resin powder having a viscosity average molecular weight of 22,500 made from bisphenol A and phosgene by a conventional method, “Panlite L-1225WP” manufactured by Teijin Chemicals Ltd.)
PC-2: Aromatic polycarbonate resin (Aromatic polycarbonate resin powder having a viscosity average molecular weight of 19,700 made from bisphenol A and phosgene by a conventional method, “Panlite L-1225WX” manufactured by Teijin Chemicals Ltd.)
(P component)
PPE: Polyphenylene ether resin ("PPE" manufactured by GEM)
(B component)
AS-1: Acrylonitrile-styrene copolymer (“HF5670” manufactured by Daiichi Koryo Co., Ltd., weight average molecular weight in terms of standard polystyrene by GPC measurement: 95,000, acrylonitrile content: 28.5 wt%, styrene content : 71.5% by weight)
AS-2: Acrylonitrile-styrene copolymer (Nippon A & L Co., Ltd. “BS-218”, weight average molecular weight in terms of standard polystyrene by GPC measurement: 78,000, acrylonitrile content: 26% by weight, styrene content: 74 weight%)
(S component)
HIPS: Polystyrene resin (“Denkastyrol GP-1” manufactured by Denki Kagaku Kogyo Co., Ltd.)
(C-1 component)
MICA-1: Mascobite with an average particle size of about 250 μm (“WHITE MICA POWDER 60 mesh” manufactured by Shaanxi Mining, Mohs hardness: 3)
MICA-2: Mascobite with an average particle diameter of about 60 μm (“WHITEMICA POWDER 250 mesh” manufactured by Shaanxi Mining, Mohs hardness: 3)
MICA-3: Mascobite having an average particle diameter of about 40 μm (“Kuralite Mica 300D, Mohs hardness: 3” manufactured by Kuraray Co., Ltd.)
MICA-4: Mascobite with an average particle size of about 40 μm (“MC-250 Mohs hardness: 3” manufactured by Hayashi Kasei Co., Ltd.)
(C-2 component)
TALC-1: Talc ("Victory Talc R" manufactured by Katsumiyama Mining Co., Ltd., stacking ratio 50%, particle size: 8.5 μm, Hunter whiteness measured according to JIS M8016: 83.8%, pH: 9.6, and Mohs hardness: 1)
TALC-2: Talc (Katsumiyama Mining Co., Ltd. “Victorylite SG-A”, stacking ratio 50% Particle size: 15.2 μm, Hunter whiteness measured according to JIS M8016: 90.2%, pH: 9.8, and Mohs hardness: 1)
WSN: Wollastonite (Kawatetsu Mining Co., Ltd. “PH-450”, number average fiber diameter: 1.6 μm, number average fiber length: 6.7 μm, Mohs hardness: 4.5])
(Inorganic filler other than the present invention)
MICA-5: Mascobite (Yamaguchi Mica “A-41” average particle diameter of about 20 μm)
GFL: Granular glass flakes (Fleka REFG-301 manufactured by Nippon Sheet Glass Co., Ltd., median average diameter 140 μm, thickness 5 μm, Mohs hardness: 6.5 by standard sieving method)
(D component)
FR-1: Resorcinol bis (dixylenyl phosphate) (Adeka Stub FP-500 manufactured by Asahi Denka Kogyo Co., Ltd., TGA 5% weight loss temperature = 351.0 ° C.) FR-2: Bisphenol A bis (diphenyl phosphate) Phosphoric acid ester (“CR-741” manufactured by Daihachi Chemical Industry Co., Ltd., TGA 5% weight loss temperature = 335.9 ° C.)
FR-3: Triphenyl phosphate (“TPP” manufactured by Daihachi Chemical Industry Co., Ltd., TGA 5% weight loss temperature = 239.4 ° C.)
(E component)
PTFE: Polytetrafluoroethylene having the ability to form fibrils (“Polyflon MPA FA500” manufactured by Daikin Industries, Ltd.)
(F component)
WAX-1: Montanate ester (“WAX-E powder” manufactured by Clariant Japan Co., Ltd.)
(Other ingredients)
WAX-2: Acid-modified polyolefin wax (Mitsubishi Kasei Corporation Diacarna 30M)
CB: Carbon Black Master (Polystyrene resin master containing 40% carbon black)
[0113]
[Table 1]

[0114]
[Table 2]

[0115]
[Table 3]

[0116]
[Table 4]

[0117]
[Table 5]

[0118]
[Table 6]

[0119]
As is clear from the above table, the flame-retardant thermoplastic resin composition of the present invention has high rigidity, high strength, high dimensional accuracy, good flame retardancy, and characteristics that make it difficult to wear the mold. I understand that.
[0120]
Furthermore, in Examples 1 and 2 of the above examples, the surface roughness was measured. From these dried pellets, a plate-like test piece having a length of 150 mm, a width of 150 mm, and a thickness of 2 mm (a gate is a fin gate having a width of 40 mm and a thickness of 1 mm from one end of the side) is prepared by injection molding, and the surface roughness is determined. It was measured. The molding conditions of the flat test piece are: injection molding machine: SG-150U manufactured by Sumitomo Heavy Industries, Ltd., cylinder temperature: 260 ° C., mold temperature: 50 ° C. (maintain the temperature applied through the 20 ° C. refrigerant by the chiller unit. ), Filling time: 6 seconds, holding pressure: 75 MPa, holding pressure time: 3 seconds, and cooling time: 20 seconds. Such a flat specimen uses a surface roughness meter Surfcom 1400A manufactured by Tokyo Seimitsu Co., Ltd., and its surface roughness was measured. As a result, in Example 1, Ra: 2.3 μm and Ry: 19.1 μm. On the other hand, in Example 2, Ra was 1.2 μm and Ry was 8.2 μm, which was very good in the mica having a smaller particle size of Example 2. Here, Ra represents the arithmetic average roughness, and Ry represents the maximum height. The measurement was performed according to JIS B0601.
[0121]
Moreover, in any of the resin compositions of Examples 1 to 11, a chassis molded product of an optical recording medium drive was molded, and a good chassis molded product was obtained.
[0122]
【The invention's effect】
The flame-retardant resin composition of the present invention can be used for any material that requires mechanical properties such as impact strength, flame retardancy, and dimensional stability. In particular, it is effective in the field of OA equipment that requires high dimensional accuracy, such as a laser beam printer optical chassis that is an optical unit chassis and a structure frame of a laser beam printer. In addition, the flame retardant resin composition of the present invention has little screw and mold wear in a molding machine and has high economic effects in molding. Therefore, the industrial effect that it plays is exceptional.
[Brief description of the drawings]
FIG. 1 is a front view showing the shape of a plate-shaped molded product for die wear evaluation used in Examples. The pin portion arranged in the vicinity of the gate forms a conical recess. [1-B] is a side view showing the shape of a plate-like molded product for die wear evaluation used in Examples. [1-C] is a bottom view showing the shape of a plate-like molded product for die wear evaluation used in Examples.
FIG. 2 is a front view showing the shape of a die wear evaluation pin used in Examples. The conical portion at the tip is exposed on the mold cavity surface and comes into contact with the molten resin.
[3-A] is a front view showing the shape of a cup-shaped molded product for releasing force evaluation used in Examples. [3-B] is a side view showing the shape of a cup-shaped molded product for releasing force evaluation used in Examples. [3-C] is a bottom view showing the shape of a cup-shaped molded product for releasing force evaluation.
[4-A] shows an outline of the mold structure used in the evaluation of the release force. The state which filled the resin in the metal mold cavity is shown. [4-B] indicates a state where the mold is cooled and opened after the filling of [4-A]. At this point, the molded product is in close contact with the movable mold. In [4-C], after the mold opening in [4-B] above, the protruding pin is pushed out by the advance of the protruding rod to release the molded product. The force at the time of ejection is detected by a load cell in contact with the ejection pin.
FIG. 5 is a perspective view showing an outline of a jig that performs three-point bending in an evaluation of low-viscosity lubricating oil resistance of a molded product, which is one of the evaluation items of the above-described embodiment.
[Explanation of symbols]
1 Plate-shaped product for die wear evaluation
2 Conical recess formed by pins
3 Gate (width 4mm, thickness 1.5mm)
4 Length of plate-shaped molded product for die wear evaluation (100mm)
5 pin distance from the gate (10mm)
6 Diameter of conical recess formed by pins (pin diameter) (10 mm)
7 Center line (The center of the pin is on the center line of the molded product)
8 Depth of conical recess formed by pins (pin height) (3 mm)
9 Thickness of plate-shaped molded product for die wear evaluation (5mm)
10 Width of plate-shaped product for die wear evaluation (50mm)
11 Pin diameter (10mm)
12 Pin conical part (mold cavity surface exposed part) height (3mm)
21 Cup-shaped molded product body
22 Distance from the axis of symmetry (26) to the part (15mm)
23
24 Heel height (20mm)
25 Cup upper surface end face (corner part R: 2.5mm)
26 Axis of symmetry
27 Internal hole (radius 1mm)
28 Z pin protrusion (radius 7.5mm from the central axis to the outer periphery)
29 Bottom of cup (corner part R: 5mm)
30 thickness (4mm)
31 Distance from the central axis (34) to the inner bottom hole (27) central axis (13mm)
32 Distance from the central axis (34) to the bottom edge of the cup (36) (26mm)
33 Distance from the central axis (34) to the top edge of the cup (25) outer edge (30mm)
34 cup central axis
35 sprue (outer radius 6 mm, tip radius 3 mm, length 39 mm)
36 Cup bottom
37 Cup bottom thickness (4mm)
38 cup outer peripheral thickness (2.5mm, all outer peripheral parts are the same)
39 cup outer wall
41 Fixed mold
42 Molded products
43 Extrusion pin (tip Z pin)
44 load cell
51 First fixing rod (made of stainless steel with a diameter of 3.9 mmφ)
52 Central part of the test piece (installed to be located at the top of the arc drawn by the test piece. Place gauze impregnated with lubricating oil on this part)
53 Moving rod for strain loading (made of stainless steel with a diameter of 3.9mmφ)
54 Screw screw for strain loading (penetrated through the back surface of the pedestal 57. The screw screw is turned from the position in contact with the unloaded test piece, and a predetermined amount of strain is loaded on the test piece based on the screw pitch)
55 Test piece (shape conforming to ASTM D638 TYPE I)
56 Second fixing rod (made of stainless steel with a diameter of 3.9 mmφ)
57 pedestal
58 Horizontal distance between the second fixed rod and the moving rod for strain load (50.0mm)
59 Horizontal distance from the first fixed rod to the moving rod for strain load (50.0mm)

Claims (16)

(A) aromatic polycarbonate resin (component A),
(B) acrylonitrile-styrene copolymer (component B),
(C) inorganic filler (component C),
(D) Organophosphorus compound flame retardant (D component) and (E) Fluorine-containing anti-dripping agent (E component)
The flame retardant aromatic polycarbonate resin composition is characterized in that the ratio of these components satisfies the following conditions (i) to (iii).
(I) The total of component A and component B is 50% by weight or more, component C is 15 to 35% by weight, and component D is 3 to 15% by weight per 100% by weight of components A to D In addition, the E component is 0.02 to 2 parts by weight per 100 parts by weight in total of the A to D components.
(Ii) A component is 75 to 95 parts by weight and B component is 5 to 25 parts by weight per 100 parts by weight of the total of A component and B component.
(Iii) C component is composed of (C1) mica (C-1 component) having an average particle size of 30 to 300 μm and (C2) wollastonite (C-2 component), and per 100% by weight of the total of A to D components. The C-1 component is 10 to 25% by weight, the C-2 component is 5 to 15% by weight, and the C-1 component is 40 to 90 per 100 parts by weight in total of the C-1 component and the C-2 component. Parts by weight. (A) aromatic polycarbonate resin (component A),
(B) acrylonitrile-styrene copolymer (component B),
(C) inorganic filler (component C),
(D) Organophosphorus compound flame retardant (D component) and (E) Fluorine-containing anti-dripping agent (E component)
(F) Higher fatty acid ester of mono- or polyhydric alcohol (F component)
The flame retardant aromatic polycarbonate resin composition is characterized in that the ratio of these components satisfies the following conditions (i) to (iii).
(I) The total of component A and component B is 50% by weight or more, component C is 15 to 35% by weight, and component D is 3 to 15% by weight per 100% by weight of components A to D The E component is 0.02 to 2 parts by weight and the F component is 0.01 to 2 parts by weight per 100 parts by weight of the A to D components.
(Ii) The A component is 75 to 95 parts by weight and the B component is 5 to 25 parts by weight per 100 parts by weight of the total of the A component and the B component.
(Iii) C component is composed of (C1) mica (C-1 component) and (C2) wollastonite (C-2 component) having an average particle size of 30 to 300 μm, and per 100% by weight of the total of A to D components. The C-1 component is 10 to 20% by weight, the C-2 component is 5 to 15% by weight, and the C-1 component is 40 to 90 per 100 parts by weight in total of the C-1 component and the C-2 component. Parts by weight.   The resin composition according to claim 1 or 2, wherein the molded product from the resin composition has a shrinkage anisotropy of 0.15 or less and an impact strength of 30 J / m or more.   The resin composition according to claim 1 or 2, wherein a molded product from the resin composition satisfies a V-1 level in a flame retardant test of a 1.6 mm thickness test piece according to UL94 standard.   The resin composition according to claim 1 or 2, wherein a molded product from the resin composition has resistance to a low-viscosity lubricating oil. The resin composition according to claim 1 or 2, wherein a molded product from the resin composition has a true density of 1.3 to 1.45 (g / cm ³ ).   The resin composition according to claim 1 or 2, wherein the acrylonitrile-styrene copolymer (component B) has a weight average molecular weight in the range of 40,000 to 200,000.   The resin composition according to claim 1 or 2, wherein the acrylonitrile-styrene copolymer (component B) has a ratio of acrylonitrile component: styrene component in the range of 5:95 to 50:50 by weight.   The resin composition according to claim 1 or 2, wherein the mica (C-1 component) in the inorganic filler (C component) has an average particle diameter in the range of 30 to 280 µm.   The resin composition according to claim 1 or 2, wherein the organophosphorus compound-based flame retardant (component D) is an organophosphate ester.   The resin composition according to claim 1 or 2, wherein the organophosphorus compound-based flame retardant (component D) has a 5% weight loss temperature in the range of 280 to 380 ° C.   The total of component A and component B is 60% by weight or more, component C is 20 to 30% by weight, component D is 3 to 10% by weight, and component A to component D per 100% by weight of component A to component D. The resin composition according to claim 1 or 2, wherein the E component is 0.1 to 1 part by weight per 100 parts by weight of the total D component.   The resin composition according to claim 1 or 2, wherein the A component is 78 to 92 parts by weight and the B component is 8 to 22 parts by weight per 100 parts by weight of the total of the A component and the B component.   C component is 12 to 20% by weight of mica (C-1 component), 5 to 12% by weight of C-2 component, and C-1 component and C per 100% by weight of A to D components in total. The resin composition according to claim 1 or 2, wherein the C-1 component is 50 to 80 parts by weight per 100 parts by weight of the total of -2 components.   A molded article formed from the resin composition according to claim 1.   A chassis or frame molded product formed from the resin composition according to claim 1.

Images