JP2008019296A - 光反射性樹脂組成物およびこれを成形してなる光反射性部材 - Google Patents
光反射性樹脂組成物およびこれを成形してなる光反射性部材 Download PDFInfo
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- JP2008019296A JP2008019296A JP2006189920A JP2006189920A JP2008019296A JP 2008019296 A JP2008019296 A JP 2008019296A JP 2006189920 A JP2006189920 A JP 2006189920A JP 2006189920 A JP2006189920 A JP 2006189920A JP 2008019296 A JP2008019296 A JP 2008019296A
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- VIQSRHWJEKERKR-UHFFFAOYSA-L disodium;terephthalate Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=C(C([O-])=O)C=C1 VIQSRHWJEKERKR-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
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- 229920006351 engineering plastic Polymers 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- KVFVBPYVNUCWJX-UHFFFAOYSA-M ethyl(trimethyl)azanium;hydroxide Chemical compound [OH-].CC[N+](C)(C)C KVFVBPYVNUCWJX-UHFFFAOYSA-M 0.000 description 1
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- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
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- YVBBRRALBYAZBM-UHFFFAOYSA-N perfluorooctane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YVBBRRALBYAZBM-UHFFFAOYSA-N 0.000 description 1
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Landscapes
- Optical Elements Other Than Lenses (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
【解決手段】 芳香族ポリカーボネート樹脂(A)30〜99重量部と、脂環式ポリエステル樹脂(B)1〜70重量部からなる樹脂成分(C)100重量部に対し、酸化チタン(D)を1〜30重量部含む、光反射性樹脂組成物。
【選択図】なし
Description
シ−3−メチルフェニル)フルオレン等で例示されるカルド構造含有ビスフェノール類;
先ず、界面重合法について説明する。界面重合法によるポリカーボネート樹脂の製造方法は、具体的には例えば、以下の方法が挙げられる。先ず、反応に不活性な、有機溶媒とアルカリ水溶液の存在下、通常pHを9以上に保ち、芳香族ジヒドロキシ化合物、及び必要に応じて分子量調整剤(末端停止剤)や芳香族ジヒドロキシ化合物の酸化防止剤等をホスゲンと反応させる。次いで第三級アミンまたは第四級アンモニウム塩等の重合触媒を添
加し、界面重合を行うことによってポリカーボネートを得る。
次に、エステル交換法について説明する。エステル交換法による反応は、カーボネート前駆体である炭酸ジエステルと、芳香族ジヒドロキシ化合物とのエステル交換反応である。炭酸ジエステルとしては、ジメチルカーボネート、ジエチルカーボネート、ジ−tert−ブチルカーボネート等の炭酸ジアルキル化合物、ジフェニルカーボネートおよびジトリルカーボネート等の置換ジフェニルカーボネート等が例示される。炭酸ジエステルは、好ましくはジフェニルカーボネートまたは置換ジフェニルカーボネートであり、より好ましくはジフェニルカーボネートである。
際には、通常、エステル交換触媒を用いる。エステル交換触媒は、特に制限はないが、アルカリ金属化合物および/またはアルカリ土類金属化合物が好ましい。また、補助的に、塩基性ホウ素化合物、塩基性リン化合物、塩基性アンモニウム化合物またはアミン系化合物などの塩基性化合物を併用することも可能である。
ウムヒドロキシド、トリエチルメチルアンモニウムヒドロキシド、トリエチルベンジルアンモニウムヒドロキシド、トリエチルフェニルアンモニウムヒドロキシド、トリブチルベンジルアンモニウムヒドロキシド、トリブチルフェニルアンモニウムヒドロキシド、テトラフェニルアンモニウムヒドロキシド、ベンジルトリフェニルアンモニウムヒドロキシド、メチルトリフェニルアンモニウムヒドロキシド、ブチルトリフェニルアンモニウムヒドロキシド等が挙げられる。
イクルされた芳香族ポリカーボネート樹脂を使用してもよい。
本発明に用いる脂環式ポリエステル樹脂(B)は、従来公知の任意のものを使用できる。中でも、1,4−シクロヘキサンジカルボン酸を主成分とするジカルボン酸成分と、ジオール成分とを反応させて得られるポリエステル樹脂であることが好ましい。この様な脂環式ポリエステル樹脂(B)は、ジカルボン酸成分を原料とするので、ジカルボン酸エステルを原料とする場合とは異なり、アルキルエステル末端が少ないので好ましい。
フェニルエーテルジカルボン酸、4,4−ジフェニルケトンジカルボン酸、4,4’−ジフェノキシエタンジカルボン酸、4,4−ジフェニルスルホンジカルボン酸、2,6−ナフタレンジカルボン酸等の芳香族ジカルボン酸、コハク酸、グルタン酸、アジピン酸、ピメリン酸、スベリン酸、アゼライン酸、セバシン酸、ウンデカジカルボン酸、ドデカジカルボン酸、及びこれらカルボン酸の炭素数1〜4のアルキルエステルやハロゲン化物等が挙げられる。
しい。更に、得られたポリエステル樹脂は必要に応じて固相重合を行い、より固有粘度の高いものとしてもよい。ここで、固有粘度は、フェノール/テトラクロロエタン(重量比1/1)混合液を溶媒としてウベローデ型粘度計を用いて30℃で測定することにより求められる。
Index(YI)が目視にても黄色着色を認識できる程高すぎると、当然、本発明の光反射性樹脂組成物が黄色くなり、反射光波長に影響を及ぼす場合がある。よって一般的にYIは18以下、中でも15以下であることが好ましい。又、YIの下限は通常−5程度である。
本発明に用いる樹脂成分(C)は、上述した芳香族ポリカーボネート樹脂(A)30〜99重量部と、脂環式ポリエステル樹脂(B)1〜70重量部からなるものである。芳香族ポリカーボネート樹脂が30重量部未満では、荷重撓み温度や剛性が低く、99重量部を越えると光線反射特性の改良効果が小さい。
本発明においては、酸化チタン(D)を用いることで、本発明の光反射性樹脂組成物、及びこれを成形してなる光反射性部材の、白度、光反射特性を向上することを特長とする。本発明に用いる酸化チタンは、従来公知の任意のものから、適宜選択して使用すればよく、その製造方法、結晶形態、平均粒子径等の形状等は、特に限定されるものではない。
部材において、光反射性や表面性の低下が生じたり、衝撃強度が低下する場合がある。よって本発明に用いる酸化チタン(D)の粒子径は、中でも0.1〜0.5μm、特に0.15〜0.35μmであることが好ましい。
よって本発明に用いる酸化チタン(D)を無機化合物によって処理する場合には、シリカを用いずに、アルミナやジルコニア等にて処理することが好ましい。
〜25重量部、特に10〜20重量部であることが好ましい。
また、本発明の光反射性樹脂組成物は、難燃性改良等を目的として、更に有機酸金属塩
(E)を含有させてもよい。本発明に用いる有機酸金属塩(E)としては、有機酸アルカリ金属塩または有機酸のアルカリ土類金属塩が挙げられる。中でも有機スルホン酸金属塩を用いることが好ましく、具体的には例えば、パーフルオロアルカンスルホン酸金属塩、パーフルオロアルキレンジスルホン酸金属塩、芳香族スルホン酸金属塩等が挙げられ、特にパーフルオロアルカンスルホン酸金属塩、パーフルオロアルキレンジスルホン酸金属塩が好ましい。また有機酸金属塩は、一種または任意の割合で二種以上を併用してもよい。
)との相溶性が低下し、樹脂成形体の外観が低下するおそれがあるので、mは中でも、1〜8であることが好ましい。
中でも0.001〜4重量部、特に0.001〜3重量部であることが好ましい。
本発明の光反射性樹脂組成物は、更に、ポリテトラフルオロエチレン(F)を含有していてもよい。本発明に用いるポリテトラフルオロエチレン(F)としては、フィブリル形
成能を有するものが好ましく、これは重合体中に容易に分散し、かつ重合体同士を結合して繊維状構造を作る傾向を示すものである。
本発明においては、更に、ポリカーボネート樹脂(A)30〜99重量部と脂環式ポリエステル樹脂(B)1〜70重量部からなる樹脂成分(C)100重量部に対し、下記一般式(I)乃至(VI)で表される化合物からなる群より選ばれる少なくとも一種のリン化合物(G)を、0.001〜1重量部含有することが好ましいし。以下、下記一般式(I)〜(VI)で表される化合物を、各々、(G−1)〜(G−6)として説明する。
本発明に用いる(G−1)リン酸エステルは、以下の一般式(I)で表されるものである。
(一般式(I)中、Rはアルキル基またはアリール基を示し、各々同一でも異なっていてもよく、nは0〜2の整数を示す。)
本発明に用いる(G−2)亜リン酸エステルは、以下の一般式(II)で表されるもの
である。
本発明に用いる(G−2)〜(G−6)の有機リン酸エステル金属塩は、以下の一般式(III)〜(VI)で表されるものである。
PC(芳香族ポリカーボネート樹脂):三菱エンジニアリングプラスチックス社製 ユーピロンS−3000FN、粘度平均分子量21000
攪拌機、還流冷却器、加熱装置、圧力計、温度計および減圧装置を装備し、容量が100リットルのステンレス製反応器に、1,4−シクロヘキサンジカルボン酸(トランス体:シス体の比率が96:4)101.5重量部、1,4−シクロヘキサンジメタノール(トランス体:シス体の比率が69:31)88.6重量部およびテトラ−n−ブチルチタネートの6重量%ブタノール溶液0.005重量部を仕込み、反応器内を窒素ガスで置換した。反応器内を窒素ガスでシールしながら、内温を30分間で150℃に昇温し、更に150℃から200℃まで1時間をかけて昇温した。
反射率:50*50*2[mm]の反射率測定試験片を用い、島津製作所社製UV−3100PC、及びMPC−3100にて測定した。尚、測定法は島津製作所社法による。
PC100重量部に対して、脂環式ポリエステル及び添加剤を表1に示す比率(重量部)で配合し、タンブラーにて15分ブレンドを行い、その後、二軸押し出し機にて300℃のシリンダー温度にて押し出しペレット化した。そのペレットを射出成形機にて280℃のシリンダー温度、80℃の金型温度にて燃焼試験片および反射率測定用に50*50mm*2mm厚の試験片を成形した。評価結果を表1に示す。
実施例1〜5と同様に、表1に示す処方の樹脂組成物から試験片を成形し、評価を行い、その結果を表1に示す。
Claims (6)
- 芳香族ポリカーボネート樹脂(A)30〜99重量部と、脂環式ポリエステル樹脂(B)1〜70重量部からなる樹脂成分(C)100重量部に対し、酸化チタン(D)を3〜30重量部含む、光反射性樹脂組成物。
- 脂環式ポリエステル樹脂(B)が、1,4−シクロヘキサンジカルボン酸成分を主成分とする脂環式ジカルボン酸と、1,4−シクロヘキサンジメタノールを主成分とする脂環式ジオールとからなる請求項1に記載の光反射性樹脂組成物。
- 樹脂成分(C)100重量部に対し、更に有機酸金属塩(E)を0.001〜5重量部含む請求項1または2に記載の光反射性樹脂組成物。
- 樹脂成分(C)100重量部に対し、更にポリテトラフルオロエチレン(F)を0.05〜1重量部含む請求項1乃至3のいずれかに記載の光反射性樹脂組成物。
- 樹脂成分(C)100重量部に対し、更に、下記一般式(I)乃至(VI)で表される化合物群より選ばれる少なくとも一種のリン化合物(G)を0.001〜1重量部含むことを特徴とする請求項1乃至4の何れかに記載の光反射性樹脂組成物。
O=P(OH)n(OR)3−n・・・(I)
(一般式(I)中、Rはアルキル基またはアリール基を示し、各々同一でも異なっていてもよく、nは0〜2の整数を示す。)
一般式(VI)
- 請求項1乃至5の何れかに記載の光反射性樹脂組成物を成形してなる光反射性部材。
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