JP2009001620A - 熱可塑性樹脂組成物および樹脂成形品 - Google Patents
熱可塑性樹脂組成物および樹脂成形品 Download PDFInfo
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- JP2009001620A JP2009001620A JP2007161780A JP2007161780A JP2009001620A JP 2009001620 A JP2009001620 A JP 2009001620A JP 2007161780 A JP2007161780 A JP 2007161780A JP 2007161780 A JP2007161780 A JP 2007161780A JP 2009001620 A JP2009001620 A JP 2009001620A
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Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
【解決手段】 芳香族ポリカーボネート樹脂(A成分)40〜99重量%と、アンチモン系化合物を重合触媒として用いて製造されたポリエチレンテレフタレート樹脂(B成分)1〜60重量%と(ただし、A成分とB成分の合計は100重量%)、特定の有機リン酸エステル化合物(C成分)0.001〜3重量部とから成る熱可塑性樹脂組成物。
【選択図】なし
Description
本発明に用いる芳香族ポリカーボネート樹脂(以下、「A成分」と略記することがある。)とは、原料として、芳香族ジヒドロキシ化合物とカーボネート前駆体とを使用し、または、これらに併せて少量のポリヒドロキシ化合物を使用して得られ、直鎖または分岐の熱可塑性の重合体または共重合体である。
本発明に用いるポリエチレンテレフタレート樹脂(以下、「B成分」と略記することがある。)とは、テレフタル酸単位およびエチレングリコール単位がエステル結合した構造を有するポリエステルであり、ジカルボン酸単位の50モル%以上がテレフタル酸単位から成り、ジオール単位の50モル%以上がエチレングリコール単位から成るアンチモン系化合物を重合触媒として用いて製造された重合体である。そして、エチレンテレフタレート単位が構成繰り返し単位の80モル%以上を占めるのが好ましく、90モル%以上を占めるのが更に好ましい。エチレンテレフタレート単位が80モル%未満では、ポリエチレンテレフタレート樹脂としての機械的性質や耐熱性などが劣る。
本発明に用いる有機リン酸エステル化合物(C成分)は、下記一般式(1)、(2)、(3)、(4)及び下記一般式(5)で表される有機リン酸エステル化合物から成る群より選ばれた少なくとも一種である有機リン酸エステル化合物であり、一般式(1)〜(5)の有機リン酸エステル化合物を二種以上組み合わせて使用してもよい。
本発明の熱可塑性樹脂組成物においては、これを構成するA成分〜C成分の含有比率は、A成分およびB成分の合計100重量%中、芳香族ポリカーボネート樹脂(A成分)が40〜99重量%、ポリエチレンテレフタレート樹脂(B成分)1〜60重量%であり、このA、B成分の合計100重量部に対して、有機リン酸エステル化合物(C成分)0.001〜3重量部である。
本発明の熱可塑性樹脂組成物には、耐衝撃性を向上させる目的でゴム性重合体(以下、「D成分」と略記することがある。)を配合することが好ましい。ゴム性重合体とは、ガラス転移温度が0℃以下、中でも−20℃以下のものを示し、ゴム性重合体にこれと共重合可能な単量体成分とを共重合した重合体をも含む。本発明に用いるゴム性重合体は、一般に芳香族ポリカーボネート樹脂に配合されて、その耐衝撃性を改良し得る、従来公知の任意のものを使用できる。
本発明の熱可塑性樹脂組成物は、必要に応じて本発明の目的を損なわない範囲において上記A、B、C、D成分以外に他の樹脂や各種樹脂添加剤を含有していてもよい。
本発明の樹脂組成物は、前記A〜C成分の他に、樹脂や添加剤などを、従来公知の任意の方法を適宜選択して、製造することができる。
表1〜表2に示す各成分を表1〜表2に示す割合にてタンブラーミキサーで均一に混合した後、二軸押出機(日本製鋼所社製、TEX30XCT、L/D=42、バレル数12)を用いて、シリンダー温度280℃、スクリュー回転数200rpm、吐出量20kg/hにてバレル1より押出機にフィードし溶融混練することにより樹脂組成物のペレットを作製した。
上記の方法で得られたペレットを、120℃で6時間以上乾燥した後、射出成形機(名機製作所製「M150AII−SJ型」)を用いて、シリンダー温度280℃、金型温度80℃、成形サイクル55秒の条件で、通常成形を行い、試験片(ASTM試験片および平板状成形品(90mm×50mm×3mm厚))を作製した。さらに、成形サイクル5分に変更した以外は上記と同様にして滞留成形を行い、5ショット目以降につき試験片(ASTM試験片および平板状成形品(90mm×50mm×3mm厚))を作製した。
樹脂組成物のペレットを110℃で6時間以上乾燥した後、高荷式フローテスターを用いて、280℃、荷重160kgf/cm2の条件下で組成物の単位時間あたりの流出量Q値(単位:cc/s)を測定し、流動性を評価した。なお、オリフィスは直径1mm×長さ10mmのものを使用した。Q値が高いほど、流動性に優れていることを示す。
ASTM D256に準拠して、厚み3.2mmの通常成形のノッチ付き試験片を用いて、23℃においてIzod衝撃強度(単位:J/m)を測定した。
ASTM D648に準拠して、通常成形のASTM試験片を用いて、1.8MPaにて熱変形温度(単位:℃)を測定した。
(a)表面外観;目視:
上記の滞留成形で作製した試験片の表面外観を目視にて観察し、シルバーストリークによる肌荒れの全くないものを◎、シルバーストリークによる肌荒れが僅かにあるものを○、シルバーストリークによる肌荒れが顕著にあるものを×として評価した。
上記の滞留成形で作製した平板状成形品について、グロスメーター(日本電色工業社製、VG2000型)を用い、測定角度60°で光沢度を測定した。光沢度が大きいほど光沢感に優れている。
上記の滞留成形で作製したASTM試験片について、ASTM D648に準拠して、1.8MPaにて熱変形温度(単位:℃)を測定した。
通常成形のASTM引張試験片(厚さ3.2mm)に変形率1%の撓みを負荷した状態で、試験薬品を塗布し、室温下1時間後に目視でクラック発生度合を評価した。試験薬品として、市販のレギュラーガソリンを使用した。なお、クラック発生度合は、試験片10本中にクラックの発生した本数の割合により評価した。
通常成形のASTM引張試験片(厚さ3.2mm)を75℃95%RHにて1000時間湿熱処理した後、引張試験を行い、処理していないものに対する破断伸び保持率にて評価した。
表1〜表2に記載の各々の樹脂組成物を製造し、上述の方法により評価した。結果を表1〜表2に示す。
Claims (9)
- 芳香族ポリカーボネート樹脂(A成分)40〜99重量%と、アンチモン系化合物を重合触媒として用いて製造されたポリエチレンテレフタレート樹脂(B成分)1〜60重量%と(ただし、A成分とB成分の合計は100重量%)、下記一般式(1)、(2)、(3)、(4)及び(5)で表される有機リン酸エステル化合物から成る群より選ばれた少なくとも一種である有機リン酸エステル化合物(C成分)0.001〜3重量部とから成る熱可塑性樹脂組成物。
- 有機リン酸エステル化合物が、前記一般式(1)で表される有機リン酸エステル化合物と前記一般式(2)で表される有機リン酸エステル化合物の混合物および/または前記一般式(5)で表される有機リン酸エステル化合物であり、かつ、前記一般式(1)、前記一般式(2)及び前記一般式(5)中のR1〜R5、Rがそれぞれ炭素数2〜25のアルキル基である請求項1に記載の熱可塑性樹脂組成物。
- 有機リン酸エステル化合物が、前記一般式(1)で表される有機リン酸エステル化合物と前記一般式(2)で表される有機リン酸エステル化合物の混合物であり、前記一般式(1)及び前記一般式(2)中のMが亜鉛である請求項2に記載の熱可塑性樹脂組成物。
- 芳香族ポリカーボネート樹脂(A成分)の配合量が55〜90重量%であり、ポリエチレンテレフタレート樹脂(B成分)の配合量が10〜45重量%(ただし、A成分とB成分の合計は100重量%)である請求項1〜3の何れかに記載の熱可塑性樹脂組成物。
- ポリエチレンテレフタレート樹脂の固有粘度が、0.95〜1.3dL/gである請求項1〜4の何れかに記載の熱可塑性樹脂組成物。
- C成分の含有量が、A成分とB成分の合計100重量部に対して0.01〜0.2重量部である請求項1〜5の何れかに記載の熱可塑性樹脂組成物。
- 更に、芳香族ポリカーボネート樹脂とポリエチレンテレフタレート樹脂の合計100重量部に対してゴム性重合体(D成分)を1〜40重量部含有する請求項1〜6の何れかに記載の熱可塑性樹脂組成物。
- ゴム性重合体がコア/シェル型グラフト共重合体である請求項7に記載の熱可塑性樹脂組成物。
- 請求項1〜8の何れかに記載の熱可塑性樹脂組成物を成形して成る樹脂成形品。
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JP2015030810A (ja) * | 2013-08-05 | 2015-02-16 | 三菱エンジニアリングプラスチックス株式会社 | ポリカーボネート樹脂組成物および成形品 |
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