JP2020083995A - 熱可塑性樹脂組成物およびその成形品 - Google Patents
熱可塑性樹脂組成物およびその成形品 Download PDFInfo
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- JP2020083995A JP2020083995A JP2018218353A JP2018218353A JP2020083995A JP 2020083995 A JP2020083995 A JP 2020083995A JP 2018218353 A JP2018218353 A JP 2018218353A JP 2018218353 A JP2018218353 A JP 2018218353A JP 2020083995 A JP2020083995 A JP 2020083995A
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Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
Description
1.主たる構成単位として、(A)(A−1)下記式(1)で表される構成単位(A−1)、(A−2)下記式(2)で表される構成単位(A−2)および(A−3)下記式(3)で表される構成単位(A−3)から構成され、全構成単位における構成単位(A−1)の割合が5〜15モル%、構成単位(A−2)の割合が20〜60モル%、構成単位(A−3)の割合が25〜75モル%のポリカーボネート共重合体(A成分)95〜60重量部および(B)ポリエステル樹脂(B成分)5〜40重量部からなるポリカーボネート樹脂組成物。
3.ポリカーボネート共重合体のガラス転移温度が140〜160℃である前項1または2に記載のポリカーボネート樹脂組成物。
4.ポリカーボネート共重合体の粘度平均分子量が15,000〜40,000である前項1〜3のいずれかに記載のポリカーボネート樹脂組成物。
5.構成単位(A−1)が、9,9−ビス(4−ヒドロキシ−3−メチルフェニル)フルオレンから誘導された構成単位である前項1〜4のいずれかに記載のポリカーボネート樹脂組成物。
6.構成単位(A−2)が、2,2−ビス(4−ヒドロキシ−3−メチルフェニル)プロパンから誘導された構成単位である前項1〜5のいずれかに記載のポリカーボネート樹脂組成物。
7.構成単位(A−3)が、2,2−ビス(4−ヒドロキシフェニル)プロパンから誘導された構成単位である前項1〜6のいずれかに記載のポリカーボネート樹脂組成物。
8.B成分が、ポリエチレンテレフタレート樹脂、ポリブチレンテレフタレート樹脂、ポリエチレンナフタレート樹脂、ポリブチレンナフタレート樹脂および非晶性ポリエステル樹脂からなる群より選ばれる前項1〜7のいずれかに記載のポリカーボネート樹脂組成物。
9.前項1〜8のいずれかに記載のポリカーボネート樹脂組成物を成形してなる成形品。
10.前項9の成形品を用いた自動車内外装部品。
本発明のポリカーボネート共重合体は、主たる構成単位として、(A−1)下記式(1)で表される構成単位(A−1)、(A−2)下記式(2)で表される構成単位(A−2)および(A−3)下記式(3)で表される構成単位(A−3)から構成される。
比粘度(ηSP)=(t−t0)/t0
[t0は塩化メチレンの落下秒数、tは試料溶液の落下秒数]
求められた比粘度(ηSP)から次の数式により粘度平均分子量Mvを算出したものである。
ηSP/c=[η]+0.45×[η]2c(但し[η]は極限粘度)
[η]=1.23×10−4Mv0.83
c=0.7
本発明のB成分として使用するポリエステル樹脂は、芳香族ジカルボン酸またはその反応性誘導体と、ジオール、またはそのエステル誘導体とを主成分とする縮合反応により得られる重合体ないしは共重合体である。
ポリエステル樹脂の含有量はA成分とB成分との合計100重量部中、5〜40重量部、好ましくは10〜35重量部、より好ましくは15〜30重量部である。含有量が下限以上では、優れた耐薬品性が発揮される。また、上限以下では、優れた耐熱性、表面硬度および剛性が得られる。
本発明の樹脂組成物には、目的に応じて添加剤を配合することができる。
(i)衝撃改質剤
本発明の樹脂組成物には、衝撃改質剤を配合することができる。本発明で用いることができる衝撃改質剤は、ガラス転移温度が10℃以下、好ましくは−10℃以下、より好ましくは−30℃以下であるゴム成分からなる重合体、並びに該ゴム成分からなる重合体に他のポリマー鎖が結合してなる共重合体が好ましく挙げられる。更にそのゴム成分がゴム質重合体100重量%中少なくとも35重量%、より好ましくは45重量%含有する重合体であることが好ましい。ゴム成分の含有量の上限は実用上90重量%程度が好ましい。
本発明の樹脂組成物には、離型剤を配合することができる。本発明に用いることができる離型剤としては公知のものが使用できる。例えば、脂肪酸エステル、ポリオレフィン系ワックス(ポリエチレンワックス、1−アルケン重合体など。酸変性などの官能基含有化合物で変性されているものも使用できる)、シリコーン化合物、フッ素化合物(ポリフルオロアルキルエーテルに代表されるフッ素オイルなど)、パラフィンワックス、蜜蝋などを挙げることができる。これらの中でも入手の容易さ、離型性および透明性の点から脂肪酸エステルが好ましい。かかる離型剤の含有量は、A成分とB成分との合計100重量部に対して、好ましくは0.005〜0.2重量部、より好ましくは0.007〜0.1重量部、さらに好ましくは0.01〜0.06重量部である。添加量が前記範囲の下限未満では、離型性の改善が十分ではない場合があり、上限を超える場合、ブリードアウトなど外観不良を起こす場合がある。
本発明の樹脂組成物には、その成形加工時の熱安定性を向上させることを主たる目的として各種のリン系安定剤を配合することができる。かかるリン系安定剤としては、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などが例示される。更にかかるリン系安定剤は第3級ホスフィンを含む。
本発明の樹脂組成物には、その成形加工時の熱安定性、および耐熱老化性を向上させることを主たる目的としてヒンダードフェノール系安定剤を配合することができる。かかるヒンダードフェノール系安定剤としては、例えば、α−トコフェロール、ブチルヒドロキシトルエン、シナピルアルコール、ビタミンE、n−オクタデシル−β−(4’−ヒドロキシ−3’,5’−ジ−tert−ブチルフェル)プロピオネート、2−tert−ブチル−6−(3’−tert−ブチル−5’−メチル−2’−ヒドロキシベンジル)−4−メチルフェニルアクリレート、2,6−ジ−tert−ブチル−4−(N,N−ジメチルアミノメチル)フェノール、3,5−ジ−tert−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、2,2’−メチレンビス(4−メチル−6−tert−ブチルフェノール)、2,2’−メチレンビス(4−エチル−6−tert−ブチルフェノール)、4,4’−メチレンビス(2,6−ジ−tert−ブチルフェノール)、2,2’−メチレンビス(4−メチル−6−シクロヘキシルフェノール)、2,2’−ジメチレン−ビス(6−α−メチル−ベンジル−p−クレゾール)2,2’−エチリデン−ビス(4,6−ジ−tert−ブチルフェノール)、2,2’−ブチリデン−ビス(4−メチル−6−tert−ブチルフェノール)、4,4’−ブチリデンビス(3−メチル−6−tert−ブチルフェノール)、トリエチレングリコール−N−ビス−3−(3−tert−ブチル−4−ヒドロキシ−5−メチルフェニル)プロピオネート、1,6−へキサンジオールビス[3−(3,5−ジ−tert−ブチル−4−ヒドロキシフェニル)プロピオネート]、ビス[2−tert−ブチル−4−メチル6−(3−tert−ブチル−5−メチル−2−ヒドロキシベンジル)フェニル]テレフタレート、3,9−ビス{2−[3−(3−tert−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]−1,1,−ジメチルエチル}−2,4,8,10−テトラオキサスピロ[5,5]ウンデカン、4,4’−チオビス(6−tert−ブチル−m−クレゾール)、4,4’−チオビス(3−メチル−6−tert−ブチルフェノール)、2,2’−チオビス(4−メチル−6−tert−ブチルフェノール)、ビス(3,5−ジ−tert−ブチル−4−ヒドロキシベンジル)スルフィド、4,4’−ジ−チオビス(2,6−ジ−tert−ブチルフェノール)、4,4’−トリ−チオビス(2,6−ジ−tert−ブチルフェノール)、2,2−チオジエチレンビス−[3−(3,5−ジ−tert−ブチル−4−ヒドロキシフェニル)プロピオネート]、2,4−ビス(n−オクチルチオ)−6−(4−ヒドロキシ−3’,5’−ジ−tert−ブチルアニリノ)−1,3,5−トリアジン、N,N’−ヘキサメチレンビス−(3,5−ジ−tert−ブチル−4−ヒドロキシヒドロシンナミド)、N,N’−ビス[3−(3,5−ジ−tert−ブチル−4−ヒドロキシフェニル)プロピオニル]ヒドラジン、1,1,3−トリス(2−メチル−4−ヒドロキシ−5−tert−ブチルフェニル)ブタン、1,3,5−トリメチル−2,4,6−トリス(3,5−ジ−tert−ブチル−4−ヒドロキシベンジル)ベンゼン、トリス(3,5−ジ−tert−ブチル−4−ヒドロキシフェニル)イソシアヌレート、トリス(3,5−ジ−tert−ブチル−4−ヒドロキシベンジル)イソシアヌレート、1,3,5−トリス(4−tert−ブチル−3−ヒドロキシ−2,6−ジメチルベンジル)イソシアヌレート、1,3,5−トリス2[3(3,5−ジ−tert−ブチル−4−ヒドロキシフェニル)プロピオニルオキシ]エチルイソシアヌレート、およびテトラキス[メチレン−3−(3’,5’−ジ−tert−ブチル−4−ヒドロキシフェニル)プロピオネート]メタンなどが例示される。これらはいずれも入手容易である。前記ヒンダードフェノール系安定剤は、単独でまたは2種以上を組合せて使用することができる。
本発明の樹脂組成物は紫外線吸収剤を含有することができる。本発明の紫外線吸収剤としては、具体的にはベンゾフェノン系では、例えば、2,4−ジヒドロキシベンゾフェノン、2−ヒドロキシ−4−メトキシベンゾフェノン、2−ヒドロキシ−4−オクトキシベンゾフェノン、2−ヒドロキシ−4−ベンジロキシベンゾフェノン、2−ヒドロキシ−4−メトキシ−5−スルホキシベンゾフェノン、2−ヒドロキシ−4−メトキシ−5−スルホキシトリハイドライドレイトベンゾフェノン、2,2’−ジヒドロキシ−4−メトキシベンゾフェノン、2,2’,4,4’−テトラヒドロキシベンゾフェノン、2,2’−ジヒドロキシ−4,4’−ジメトキシベンゾフェノン、2,2’−ジヒドロキシ−4,4’−ジメトキシ−5−ソジウムスルホキシベンゾフェノン、ビス(5−ベンゾイル−4−ヒドロキシ−2−メトキシフェニル)メタン、2−ヒドロキシ−4−n−ドデシルオキシベンソフェノン、および2−ヒドロキシ−4−メトキシ−2’−カルボキシベンゾフェノンなどが例示される。
本発明の樹脂組成物には、ポリカーボネート樹脂の難燃剤として知られる各種の化合物が配合されてよい。難燃剤として使用される化合物の配合は難燃性の向上のみならず、各化合物の性質に基づき、例えば帯電防止性、流動性、剛性、および熱安定性の向上などがもたらされる。
本発明の樹脂組成物には、滴下防止剤を含むことができる。かかる滴下防止剤を上記難燃剤と併用することにより、より良好な難燃性を得ることができる。かかる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かできるが、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。
本発明の樹脂組成物には、帯電防止性能が求められる場合があり、かかる場合帯電防止剤を含むことが好ましい。かかる帯電防止剤としては、例えば(1)ドデシルベンゼンスルホン酸ホスホニウム塩に代表されるアリールスルホン酸ホスホニウム塩、およびアルキルスルホン酸ホスホニウム塩などの有機スルホン酸ホスホニウム塩、並びにテトラフルオロホウ酸ホスホニウム塩の如きホウ酸ホスホニウム塩が挙げられる。該ホスホニウム塩の含有量は、A成分とB成分との合計100重量部を基準として5重量部以下が適切であり、好ましくは0.05〜5重量部、より好ましくは1〜3.5重量部、更に好ましくは1.5〜3重量部の範囲である。
本発明の樹脂組成物には、上記記載の添加剤の他に、蛍光染料、蛍光増白剤、無機系蛍光体(例えばアルミン酸塩を母結晶とする蛍光体)、ブルーイング剤、流動パラフィンの如き分散剤、熱線吸収剤およびフォトクロミック剤などを配合することができる。
本発明の樹脂組成物の製造に当たっては、その製造方法は特に限定されるものではなく公知の製造方法を利用することができる。通常、ポリカーボネート共重合体および添加剤を予備混合した後、押出機に投入して溶融混練した後、押出されたスレッドを冷却し、ペレタイザーにより切断して、ペレット状の成形材料が製造される。押出機は単軸押出機、および二軸押出機のいずれもが利用できるが、生産性や混練性の観点からは二軸押出機が好ましい。かかる二軸押出機の代表的な例としては、ZSK(Werner & Pfleiderer社製、商品名)を挙げることができる。同様のタイプの具体例としてはTEX((株)日本製鋼所製、商品名)、TEM(東芝機械(株)製、商品名)、KTX((株)神戸製鋼所製、商品名)などを挙げることができる。押出機としては、原料中の水分や、溶融混練樹脂から発生する揮発ガスを脱気できるベントを有するものが好ましく使用できる。ベントからは発生水分や揮発ガスを効率よく押出機外部へ排出するための真空ポンプが好ましく設置される。また押出原料中に混入した異物などを除去するためのスクリーンを押出機ダイス部前のゾーンに設置し、異物を樹脂組成物から取り除くことも可能である。かかるスクリーンとしては金網、スクリーンチェンジャー、焼結金属プレート(ディスクフィルターなど)などを挙げることができる。
(1)粘度平均分子量
比粘度(ηSP)を20℃で塩化メチレン100mlにポリカーボネート共重合体0.7gを溶解した溶液からオストワルド粘度計を用いて求め、比粘度(ηSP)から次の数式により粘度平均分子量(Mv)を算出した。
比粘度(ηSP)=(t−t0)/t0
[t0は塩化メチレンの落下秒数、tは試料溶液の落下秒数]
ηSP/c=[η]+0.45×[η]2c(但し[η]は極限粘度)
[η]=1.23×10−4Mv0.83
c=0.7
(2)組成比
ポリカーボネート共重合体40mgを0.6ml重クロロホルム溶液に溶解し、日本電子製400MHzの核磁気共鳴装置により、1H−NMRを測定し、各構成単位に特徴のあるスペクトルピーク面積比により、ポリカーボネート共重合体の組成比を算出した。
(3)ガラス転移温度
TAインスツルメント社製の熱分析システムDSC−2910を使用して、JIS K7121に従い窒素雰囲気下(窒素流量:40ml/min)、昇温速度:20℃/minの条件下で測定した。
(4)表面硬度(鉛筆硬度)
算術平均粗さ(Ra)が0.03μmとしたキャビティ面を持つ金型を使用し、住友重機械工業社製射出成形機SG260M−HPを用いて、シリンダー温度280℃、金型温度70℃の条件で、保圧時間10秒および冷却時間20秒にて幅50mm、長さ90mm、厚みがゲート側から3mm(長さ20mm)、2mm(長さ45mm)、1mm(長さ25mm)である3段型プレートを成形した。かかる3段プレートの厚み2mm部における鉛筆硬度をJIS K5600に則して測定した。
(5)耐熱性
ペレットを120℃で5時間乾燥後、住友重機械工業社製射出成形機SG260M−HPにより、シリンダー温度280℃で成形した試験片を用い、ISO75−1およびISO75−2に則して荷重たわみ温度を測定した。荷重:1.80MPa。(試験片形状:長さ80mm×幅10mm×厚み4mm)
(6)剛性(曲げ弾性率)
ペレットを120℃で5時間乾燥後、住友重機械工業社製射出成形機SG260M−HPにより、シリンダー温度280℃で成形した試験片を用い、ISO178に則して曲げ弾性率を測定した。(試験片形状:長さ80mm×幅10mm×厚み4mm)
(7)耐薬品性
ペレットを120℃で5時間乾燥後、住友重機械工業社製射出成形機SG260M−HPにより、シリンダー温度280℃で成形した試験片を用い、3点曲げ試験法にて、所定の歪みをかけた後、マジックリン(花王(株)製)を含侵させた布をかけ、23℃で24時間放置した後に、クラック発生の有無を確認した。クラックが発生しない最大歪みから、次の数式により限界応力を算出した。
[限界応力](MPa)=[曲げ弾性率](MPa)×[歪み](%)/100
表1の組成で得られたパウダーに、表2および3に記載した組成でA成分およびB成分を均一に混合した後、かかるパウダーをベント式二軸押出機[(株)神戸製鋼所製KTX−46]により脱気しながら溶融混錬後、ポリカーボネート樹脂組成物を得た。得られた樹脂組成物について、上記記載の方法で表面硬度、耐熱性、剛性、耐薬品性を評価した。結果を表2および3に示した。
(PC−1)
温度計、撹拌機および還流冷却器の付いた反応器に、48%水酸化ナトリウム水溶液4,555部およびイオン交換水22,730部を仕込み、これに9,9−ビス(4−ヒドロキシ−3−メチルフェニル)フルオレン(本州化学製)596部、ビスフェノールC(本州化学製)1,213部、ビスフェノールA(新日鐵化学製)2,159部、およびハイドロサルファイト7.94部(和光純薬製)を溶解した後、塩化メチレン13,415部を加え、撹拌下、15〜25℃でホスゲン2,000部を約70分かけて吹き込んだ。ホスゲンの吹き込み終了後、48%水酸化ナトリウム水溶液650部およびp−tert−ブチルフェノール89.9部を加え、撹拌を再開、乳化後トリエチルアミン3.94部を加え、さらに28〜35℃で1時間撹拌して反応を終了した。
ビスフェノールC(本州化学製)1,618部、ビスフェノールA(新日鐵化学製)1,799部、p−tert−ブチルフェノール87.6部とした以外は(PC−1)と同様の手法にてポリカーボネート共重合体パウダーを得た。得られたポリカーボネート共重合体の組成比、粘度平均分子量、およびガラス転移温度の測定結果を表1に示した。
ビスフェノールC(本州化学製)2,023部、ビスフェノールA(新日鐵化学製)1,440部、p−tert−ブチルフェノール82.8部とした以外は(PC−1)と同様の手法にてポリカーボネート共重合体パウダーを得た。得られたポリカーボネート共重合体の組成比、粘度平均分子量、およびガラス転移温度の測定結果を表1に示した。
9,9−ビス(4−ヒドロキシ−3−メチルフェニル)フルオレン(本州化学製)298部、ビスフェノールC(本州化学製)1,820部、ビスフェノールA(新日鐵化学製)1,799部、p−tert−ブチルフェノール71.0部とした以外は(PC−1)と同様の手法にてポリカーボネート共重合体パウダーを得た。得られたポリカーボネート共重合体の組成比、粘度平均分子量、およびガラス転移温度の測定結果を表1に示した。
9,9−ビス(4−ヒドロキシ−3−メチルフェニル)フルオレン(本州化学製)894部、ビスフェノールC(本州化学製)1,213部、ビスフェノールA(新日鐵化学製)1,979部、p−tert−ブチルフェノール106.5部とした以外は(PC−1)と同様の手法にてポリカーボネート共重合体パウダーを得た。得られたポリカーボネート共重合体の組成比、粘度平均分子量、およびガラス転移温度の測定結果を表1に示した。
温度計、撹拌機および還流冷却器の付いた反応器に、48%水酸化ナトリウム水溶液4,555部およびイオン交換水22,730部を仕込み、これに、ビスフェノールC(本州化学製)2,023部、ビスフェノールA(新日鐵化学製)1,799部、およびハイドロサルファイト7.94部(和光純薬製)を溶解した後、塩化メチレン13,415部を加え、撹拌下、15〜25℃でホスゲン2,000部を約70分かけて吹き込んだ。ホスゲンの吹き込み終了後、48%水酸化ナトリウム水溶液650部およびp−tert−ブチルフェノール89.9部を加え、撹拌を再開、乳化後トリエチルアミン3.94部を加え、さらに28〜35℃で1時間撹拌して反応を終了した。
9,9−ビス(4−ヒドロキシ−3−メチルフェニル)フルオレン(本州化学製)179部、ビスフェノールC(本州化学製)2,023部、ビスフェノールA(新日鐵化学製)1,691部、p−tert−ブチルフェノール92.3部とした以外は(PC−1)と同様の手法にてポリカーボネート共重合体パウダーを得た。得られたポリカーボネート共重合体の組成比、粘度平均分子量、およびガラス転移温度の測定結果を表1に示した。
9,9−ビス(4−ヒドロキシ−3−メチルフェニル)フルオレン(本州化学製)1,193部、ビスフェノールC(本州化学製)1,618部、ビスフェノールA(新日鐵化学製)1,439部、p−tert−ブチルフェノール92.3部とした以外は(PC−1)と同様の手法にてポリカーボネート共重合体パウダーを得た。得られたポリカーボネート共重合体の組成比、粘度平均分子量、およびガラス転移温度の測定結果を表1に示した。
ビスフェノールAを使用せず、9,9−ビス(4−ヒドロキシ−3−メチルフェニル)フルオレン(本州化学製)566部、ビスフェノールC(本州化学製)3,452部、p−tert−ブチルフェノール80.1部とした以外は(PC−1)と同様の手法にてポリカーボネート共重合体パウダーを得た。得られたポリカーボネート共重合体の組成比、粘度平均分子量、およびガラス転移温度の測定結果を表1に示した。
ビスフェノールCを使用せず、9,9−ビス(4−ヒドロキシ−3−メチルフェニル)フルオレン(本州化学製)596部、ビスフェノールA(新日鐵化学製)3,238部、p−tert−ブチルフェノール71.0部とした以外は(PC−1)と同様の手法にてポリカーボネート共重合体パウダーを得た。得られたポリカーボネート共重合体の組成比、粘度平均分子量、およびガラス転移温度の測定結果を表1に示した。
9,9−ビス(4−ヒドロキシ−3−メチルフェニル)フルオレン(本州化学製)を使用せず、ビスフェノールC(本州化学製)2,023部、ビスフェノールA(新日鐵化学製)1,799部、p−tert−ブチルフェノール87.6部とした以外は(PC−1)と同様の手法にてポリカーボネート共重合体パウダーを得た。得られたポリカーボネート共重合体の組成比、粘度平均分子量、およびガラス転移温度の測定結果を表1に示した。
PET:ポリエチレンテレフタレート樹脂(南亞製TRN−8550FF(商品名))
PBT:ポリブチレンテレフタレート樹脂(ポリプラスチックス製ジュラネックス500FP EF202X(商品名))
PEN:ポリエチレンナフタレート樹脂(帝人製テオネックスTN−8065S(商品名))
PBN:ポリブチレンナフタレート樹脂(帝人製PBN樹脂TQB−OT(商品名))
PCTG:非晶性ポリエステル樹脂(イーストマンケミカル製Tritan TX−1000(商品名))
Claims (10)
- (A)主たる構成単位として、(A−1)下記式(1)で表される構成単位(A−1)、(A−2)下記式(2)で表される構成単位(A−2)および(A−3)下記式(3)で表される構成単位(A−3)から構成され、全構成単位における構成単位(A−1)の割合が5〜15モル%、構成単位(A−2)の割合が20〜60モル%、構成単位(A−3)の割合が25〜75モル%のポリカーボネート共重合体(A成分)95〜60重量部および(B)ポリエステル樹脂(B成分)5〜40重量部からなるポリカーボネート樹脂組成物。
- 式(1)におけるR1およびR2は夫々独立して水素原子、炭素原子数1〜6のアルキル基であり、式(2)におけるR3およびR4は夫々独立して炭素原子数1〜6のアルキル基であり、Xは単結合、置換もしくは無置換の炭素原子数1〜10のアルキレン基、置換もしくは無置換の炭素原子数1〜10のアルキリデン基であり、式(3)におけるWは単結合、置換もしくは無置換の炭素原子数1〜10のアルキレン基、置換もしくは無置換の炭素原子数1〜10のアルキリデン基である請求項1記載のポリカーボネート樹脂組成物。
- ポリカーボネート共重合体のガラス転移温度が140〜160℃である請求項1または2に記載のポリカーボネート樹脂組成物。
- ポリカーボネート共重合体の粘度平均分子量が15,000〜40,000である請求項1〜3のいずれかに記載のポリカーボネート樹脂組成物。
- 構成単位(A−1)が、9,9−ビス(4−ヒドロキシ−3−メチルフェニル)フルオレンから誘導された構成単位である請求項1〜4のいずれかに記載のポリカーボネート樹脂組成物。
- 構成単位(A−2)が、2,2−ビス(4−ヒドロキシ−3−メチルフェニル)プロパンから誘導された構成単位である請求項1〜5のいずれかに記載のポリカーボネート樹脂組成物。
- 構成単位(A−3)が、2,2−ビス(4−ヒドロキシフェニル)プロパンから誘導された構成単位である請求項1〜6のいずれかに記載のポリカーボネート樹脂組成物。
- B成分が、ポリエチレンテレフタレート樹脂、ポリブチレンテレフタレート樹脂、ポリエチレンナフタレート樹脂、ポリブチレンナフタレート樹脂および非晶性ポリエステル樹脂からなる群より選ばれる樹脂である請求項1〜7のいずれかに記載のポリカーボネート樹脂組成物。
- 請求項1〜8のいずれかに記載のポリカーボネート樹脂組成物を成形してなる成形品。
- 請求項9の成形品を用いた自動車内外装部品。
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