JPH06306266A - Light-diffusing polycarbonate resin composition - Google Patents

Light-diffusing polycarbonate resin composition

Info

Publication number
JPH06306266A
JPH06306266A JP5122038A JP12203893A JPH06306266A JP H06306266 A JPH06306266 A JP H06306266A JP 5122038 A JP5122038 A JP 5122038A JP 12203893 A JP12203893 A JP 12203893A JP H06306266 A JPH06306266 A JP H06306266A
Authority
JP
Japan
Prior art keywords
polycarbonate resin
light
resin composition
diffusing
pts
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
JP5122038A
Other languages
Japanese (ja)
Inventor
Fumio Ooshi
文男 大士
Masaki Kuriyama
昌樹 栗山
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Steel Chemical and Materials Co Ltd
Original Assignee
Nippon Steel Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Steel Chemical Co Ltd filed Critical Nippon Steel Chemical Co Ltd
Priority to JP5122038A priority Critical patent/JPH06306266A/en
Publication of JPH06306266A publication Critical patent/JPH06306266A/en
Withdrawn legal-status Critical Current

Links

Abstract

PURPOSE:To provide a polycarbonate resin composition containing a specific inorganic compound, exhibiting light-diffusibility and opaque white translucency, free from excessive depression of melt-viscosity of a polycarbonate resin used as the base resin and preventing the surface roughening caused by the secondary agglomeration of the light-diffusing agent. CONSTITUTION:A light-diffusing polycarbonate resin composition is produced by compounding 100 pts.wt. of a polycarbonate resin with 0.5-10 pts.wt. of precipitated barium sulfate having an average particle diameter of 0.1-20mum and pH of 3.0-7.5. A light-diffusing, opaque white translucent polycarbonate resin composition is produced by compounding the above light-diffusing resin composition with 0.001-0.2 pts.wt. of titanium oxide based on 100 pts.wt. of the polycarbonate resin.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、特定の無機化合物を含
有せしめ、光拡散性、さらには乳白色半透明を示すポリ
カーボネート樹脂組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a polycarbonate resin composition containing a specific inorganic compound and exhibiting light diffusivity and translucency of milky white.

【0002】[0002]

【従来の技術】ポリカーボネート樹脂は耐衝撃性、耐熱
性、耐候性等に優れている上、高い光透過率を備えた樹
脂として各種の用途に使用されている。それらのうち、
各種照明器具カバー、工場内外を遮り光を取り入れる透
光板等においては半透明の材料が要求されることがあ
る。この種の用途に適する材料として、従来、炭酸カル
シウムと酸化チタンを併用してなるポリカーボネート組
成物が提案(特公昭57−24816号公報)されてい
る。しかし、この特公昭57−24816号公報に記載
されたポリカーボネート組成物は、製品製造工程におい
てポリカーボネートの溶融粘度を著しく低下させるた
め、押出成形に於いては成形条件が安定せず良好な表面
状態の成形品が得られない。又、射出成形に於いては成
形可能な温度範囲が狭いため、成形不良、金型の破損な
どの問題が発生しやすいという欠点があった。さらに、
該提案に於いて使用されている炭酸カルシウムは、二次
凝集を生じやすいために光沢のある良表面状態の製品を
得るのが困難である等、多くの欠点を有していた。
2. Description of the Related Art Polycarbonate resins have excellent impact resistance, heat resistance, weather resistance and the like, and are used in various applications as resins having high light transmittance. Of them
A semi-transparent material may be required for various lighting fixture covers, translucent plates that block light inside and outside the factory to take in light. As a material suitable for this kind of use, a polycarbonate composition comprising calcium carbonate and titanium oxide in combination has been proposed (Japanese Patent Publication No. 57-24816). However, since the polycarbonate composition described in JP-B-57-24816 significantly lowers the melt viscosity of the polycarbonate in the product manufacturing process, the molding conditions are not stable in extrusion molding and a good surface condition is obtained. Molded product cannot be obtained. In addition, in injection molding, since the temperature range in which molding is possible is narrow, there is a drawback that problems such as defective molding and damage to the mold are likely to occur. further,
The calcium carbonate used in the proposal had many drawbacks such as difficulty in obtaining a product having a good glossy surface condition because secondary aggregation was likely to occur.

【0003】[0003]

【発明が解決しようとする課題】本発明は、ベース樹脂
であるポリカーボネート樹脂の溶融粘度を顕著に低下さ
せず、又、光拡散剤の2次凝集による表面の荒れを無く
した光拡散性を有したポリカーボネート樹脂組成物を提
供することを課題とする。
DISCLOSURE OF THE INVENTION The present invention has a light diffusivity that does not significantly lower the melt viscosity of a polycarbonate resin that is a base resin and that eliminates surface roughness due to secondary aggregation of a light diffusing agent. It is an object of the present invention to provide the above polycarbonate resin composition.

【0004】[0004]

【課題を解決するための手段】このような問題を解決す
べく鋭意研究した結果、ポリカーボネート樹脂100重
量部に対して平均粒子径0.1〜20μm、pH3.0
〜7.5の範囲の沈降性硫酸バリウムを分散添加せしめ
たポリカーボネート樹脂組成物が溶融粘度の低下が殆ど
なく、優れた光拡散性を発現することができることを見
いだした。
As a result of intensive studies to solve such problems, an average particle diameter of 0.1 to 20 μm and a pH of 3.0 with respect to 100 parts by weight of a polycarbonate resin.
It was found that the polycarbonate resin composition to which the precipitated barium sulfate in the range of ˜7.5 is dispersedly added can exhibit an excellent light diffusivity with almost no decrease in melt viscosity.

【0005】以下、本発明を具体的に説明する。 本発
明において使用される芳香族ポリカーボネートとは、種
々のジヒドロキシジアリール化合物とホスゲンとを反応
させるホスゲン法、またはジヒドロキシジアリール化合
物とジフェニルカーボネートなどの炭酸エステルとを反
応させるエステル交換法によって得られる重合体であ
り、代表的なものとしては、2,2−ビス(4−ヒドロ
キシフェニル)プロパン2,2−ビス(4−ヒドロキシ
フェニル)プロパン (ビスフェノール A)から製造
されたポリカーボネートが挙げられる。
The present invention will be specifically described below. The aromatic polycarbonate used in the present invention is a polymer obtained by a phosgene method of reacting various dihydroxydiaryl compounds with phosgene, or a transesterification method of reacting a dihydroxydiaryl compound with a carbonic acid ester such as diphenyl carbonate. As a typical example, there is a polycarbonate produced from 2,2-bis (4-hydroxyphenyl) propane 2,2-bis (4-hydroxyphenyl) propane (bisphenol A).

【0006】上記ジヒドロキシジアリール化合物として
は、ビスフェノールAの他に、ビス(4−ヒドロキシフ
ェニル)メタン、1,1−ビス(4−ヒドロキシフェニ
ル)エタン 、2,2−ビス(4−ヒドロキシフェニ
ル)ブタン、2,2−ビス(4−ヒドロキシフェニル)
オクタン、ビス(4−ヒドロキシフェニル)フェニルメ
タン 、2,2−ビス(4−ヒドロキシフェニル−3−
メチルフェニル)プロパン 、1,1−ビス(4−ヒド
ロキシ−3−第三ブチルフェニル)プロパン、2,2−
ビス(4−ヒドロキシ−3−ブロモフェニル)プロパン
、2,2−ビス(4−ヒドロキシ−3,5−ジブロモ
フェニル)プロパン、2,2−ビス(4−ヒドロキシ−
3,5−ジクロロフェニル)プロパンのようなビス(ヒ
ドロキシアリール)アルカン類、1,1−ビス(4−ヒ
ドロキシフェニル)シクロペンタン、1,1−ビス(4
−ヒドロキシフェニル)シクロヘキサンのようなビス
(ヒドロキシアリール)シクロアルカン類、4,4’−
ジヒドロキシジフェニルエーテル、4,4’−ジヒドロ
キシ−3,3’−ジメチルジフェニルエーテルのような
ジヒドロキシジアリールエーテル類、4,4’−ジヒド
ロキシジフェニルスルフィド 、4,4’−ジヒドロキ
シ−3,3’−ジメチルジフェニルスルフィドのような
ジヒドロキシジアリールスルフィド類、4,4’−ジヒ
ドロキシジフェニルスルホキシド、4,4’−ジヒドロ
キシ−3,3’−ジメチルジフェニルスルホキシドのよ
うなジヒドロキシジアリールスルホキシド類、4,4’
−ジヒドロキシジフェニルスルホン、4,4’−ジヒド
ロキシ−3,3’−ジメチルジフェニルスルホンのよう
なジヒドロキシジアリールスルホン 類等が挙げられ
る。これらは単独または2種類以上混合して使用される
が、これらの他に、ピペラジン、ジピペリジルハイドロ
キノン 、レゾルシン 、4,4’−ジヒドロキシフェ
ニル等を混合して使用してもよい。
Examples of the dihydroxydiaryl compound include bis (4-hydroxyphenyl) methane, 1,1-bis (4-hydroxyphenyl) ethane, and 2,2-bis (4-hydroxyphenyl) butane, in addition to bisphenol A. , 2,2-bis (4-hydroxyphenyl)
Octane, bis (4-hydroxyphenyl) phenylmethane, 2,2-bis (4-hydroxyphenyl-3-)
Methylphenyl) propane, 1,1-bis (4-hydroxy-3-tert-butylphenyl) propane, 2,2-
Bis (4-hydroxy-3-bromophenyl) propane, 2,2-bis (4-hydroxy-3,5-dibromophenyl) propane, 2,2-bis (4-hydroxy-)
Bis (hydroxyaryl) alkanes such as 3,5-dichlorophenyl) propane, 1,1-bis (4-hydroxyphenyl) cyclopentane, 1,1-bis (4
Bis (hydroxyaryl) cycloalkanes such as -hydroxyphenyl) cyclohexane, 4,4'-
Dihydroxy diphenyl ether, dihydroxy diaryl ethers such as 4,4'-dihydroxy-3,3'-dimethyldiphenyl ether, 4,4'-dihydroxydiphenyl sulfide, 4,4'-dihydroxy-3,3'-dimethyldiphenyl sulfide Such dihydroxydiaryl sulfides, 4,4′-dihydroxydiphenyl sulfoxide, 4,4′-dihydroxy-3,3′-dimethyldiphenyl sulfoxide such as 4,4 ′
-Dihydroxy diphenyl sulfones, dihydroxy diaryl sulfones such as 4,4'-dihydroxy-3,3'-dimethyldiphenyl sulfone, and the like. These may be used alone or in admixture of two or more, but in addition to these, piperazine, dipiperidyl hydroquinone, resorcin, 4,4'-dihydroxyphenyl and the like may be mixed and used.

【0007】さらに、上記のジヒドロキシアリール化合
物と以下に示すような3価以上のフェノール化合物を混
合使用してもよい。
Further, the above-mentioned dihydroxyaryl compound and a phenol compound having a valence of 3 or more as shown below may be mixed and used.

【0008】3価以上のフェノールとしてはフロログル
シン、4,6−ジメチル−2,4,6−トリ−(4−ヒ
ドロキシフェニル)−ヘプテン,4,6−ジメチル−
2,4,6−トリ−(4−ヒドロキシフェニル)−ヘプ
タン、1,3,5−トリ−(4−ヒドロキシフェニル)
−ベンゾール、1,1,1−トリ−(4−ヒドロキシフ
ェニル)−エタンおよび2,2−ビス−〔4,4−
(4,4’−ジヒドロキシジフェニル)−シクロヘキシ
ル〕−プロパンなどが挙げられる。ポリカーボネートの
粘度平均分子量は通常10,000 〜100,00
0、好ましくは15,000〜35,000である。か
かるポリカーボネートを製造するに際し、分子量調節
剤、触媒等を必要に応じて使用することができる。
As trihydric or higher phenols, phloroglucin, 4,6-dimethyl-2,4,6-tri- (4-hydroxyphenyl) -heptene, 4,6-dimethyl-
2,4,6-tri- (4-hydroxyphenyl) -heptane, 1,3,5-tri- (4-hydroxyphenyl)
-Benzol, 1,1,1-tri- (4-hydroxyphenyl) -ethane and 2,2-bis- [4,4-
(4,4′-dihydroxydiphenyl) -cyclohexyl] -propane and the like. The viscosity average molecular weight of polycarbonate is usually 10,000 to 100,000.
It is 0, preferably 15,000 to 35,000. In producing such a polycarbonate, a molecular weight modifier, a catalyst and the like can be used if necessary.

【0009】本発明の沈降性硫酸バリウムは、一般に工
業的に用いられている方法によって得られるもので、例
えば重晶石の還元培焼によって得られた硫化バリウムの
溶液に硫酸ナトリウム溶液を加え沈殿させて製造された
ものが挙げられ、pHが3.0〜7.5、より好ましく
は5.0〜6.5の範囲にあることが望ましい。また、
本発明に用いる平均粒子径は0.1〜20μmの範囲に
あることが必要であり、特に1〜15μmのものが好ま
しい。平均粒子径が0.1μm未満であるとポリカーボ
ネートに分散添加せしめたとき、有効な光拡散性が得ら
れない。また、平均粒子径が20μmを越えるとポリカ
ーボネートの特徴である耐衝撃性が顕著に低下してしま
う。そして、ポリカーボネート樹脂100重量部に対し
て、沈降性硫酸バリウムの添加量が0.5重量部未満で
あると有効な光拡散性が得られない。そのため、樹脂組
成物を用いて製造された成形品を通して反対側にある物
体を見たとき、その物体の形状が明確になってしまい、
いわゆる磨りガラス代替用途には不向きとなる。又、1
0重量部より多く添加しても、全光線透過率、光拡散透
過率が低くなってしまい当初の目的を達成することがで
きなくなる。
The precipitated barium sulfate of the present invention is obtained by a method which is generally used industrially. For example, a sodium sulfate solution is added to a barium sulfide solution obtained by reduction barite burning of barite to cause precipitation. It is desirable that the pH is in the range of 3.0 to 7.5, and more preferably 5.0 to 6.5. Also,
The average particle diameter used in the present invention is required to be in the range of 0.1 to 20 μm, and particularly preferably 1 to 15 μm. When the average particle diameter is less than 0.1 μm, effective light diffusion cannot be obtained when dispersed and added to polycarbonate. On the other hand, if the average particle size exceeds 20 μm, the impact resistance, which is a characteristic of polycarbonate, is significantly reduced. If the amount of the precipitated barium sulfate added is less than 0.5 parts by weight with respect to 100 parts by weight of the polycarbonate resin, effective light diffusivity cannot be obtained. Therefore, when you look at the object on the other side through the molded product manufactured using the resin composition, the shape of the object becomes clear,
It is not suitable as a so-called ground glass substitute application. Again 1
Even if added in an amount of more than 0 parts by weight, the total light transmittance and the light diffusion transmittance will be low, and the original purpose cannot be achieved.

【0010】また、本発明でいう沈降性硫酸バリウムの
pHとは、沈降性硫酸バリウム5gを三角フラスコ(1
00cc)にとり、水50ccを加えて5分間煮沸し、
減量分はあらかじめ煮沸した水を加えて、20℃に冷却
後、ガラス電極pH計を用いて、JIS・Z−8802
pH測定法により、測定した値である。測定は約20℃
で10分以内に終わるようにする。このようにして測定
したpHの値が3.0に満たない場合は得られる光拡散
性を有するポリカーボネートが、黄色を帯びてしまう。
一方pHの値が7.5を越える場合は光拡散性を有する
ポリカーボネートの溶融粘度が低下して成形時のトラブ
ル発生につながり、いずれも本発明の目的を達成するこ
とが困難となる。
The pH of the precipitated barium sulfate referred to in the present invention means that 5 g of precipitated barium sulfate is added to an Erlenmeyer flask (1
00cc), add 50cc of water and boil for 5 minutes,
To reduce the amount, add boiled water in advance and cool to 20 ° C., then use a glass electrode pH meter to measure JIS Z-8802.
It is the value measured by the pH measuring method. Measurement is about 20 ℃
Try to finish within 10 minutes. When the pH value measured in this way is less than 3.0, the obtained light-diffusing polycarbonate becomes yellowish.
On the other hand, when the pH value exceeds 7.5, the melt viscosity of the polycarbonate having a light diffusing property lowers, which causes troubles during molding, and it becomes difficult to achieve the object of the present invention.

【0011】又、本発明で用いられる酸化チタンの平均
粒子径に制限はないが、最終組成の透明性、光拡散性の
面より0.05〜1μm が好ましい。酸化チタンの平均
粒子径が0.05μm 〜1μm の場合には、有効な乳白
色半透明性を得る上で、特に良好な相乗効果が付与でき
る。ポリカーボネートと上記化合物との混合方法ならび
に混合順序には特に制限はなく、公知の混合機、例えば
タンブラー、ヘンシェルミキサー等で混合し、溶融混練
して行なうことができる。
The average particle size of titanium oxide used in the present invention is not limited, but it is preferably 0.05 to 1 μm from the viewpoint of transparency and light diffusion of the final composition. When the average particle diameter of titanium oxide is 0.05 μm to 1 μm, a particularly good synergistic effect can be imparted in obtaining effective milky white translucency. There is no particular limitation on the mixing method and the mixing order of the polycarbonate and the above compounds, and they can be mixed by a known mixer such as a tumbler or a Henschel mixer and melt-kneaded.

【0012】なお、混合時、必要に応じて公知の添加
剤、例えば離型剤、帯電防止剤、酸化防止剤、紫外線吸
収剤、難燃剤、染顔料等を配合することができる。
At the time of mixing, known additives such as a release agent, an antistatic agent, an antioxidant, an ultraviolet absorber, a flame retardant, a dye and pigment may be added, if necessary.

【0013】以下に本発明を実施例により具体的に説明
するが、それら実施例に限定されるものではない。ま
た”部”は重量基準に基づく。
The present invention will be specifically described below with reference to examples, but the invention is not limited to these examples. "Parts" are based on weight basis.

【0014】[0014]

【実施例】実施例及び比較例で用いた材料は以下のとお
りである。 PC:粘度平均分子量3万、 MFR=2.6g/10min(MFRの測定条件28
0℃、2.16kgf) 硫酸バリウム :pH7.0 、平均粒子径 8.1
μm 硫酸バリウム :pH4.1 、平均粒子径 2.6
μm 硫酸バリウム :pH2.5 、平均粒子径 6.3
μm 硫酸バリウム :pH8.2 、平均粒子径 4.5
μm 炭酸カルシウム :平均粒子径4.9μm 酸化チタン :平均粒子径0.25μm
EXAMPLES Materials used in Examples and Comparative Examples are as follows. PC: viscosity average molecular weight 30,000, MFR = 2.6 g / 10 min (MFR measurement condition 28
0 ° C., 2.16 kgf) Barium sulfate: pH 7.0, average particle size 8.1
μm Barium sulfate: pH 4.1, average particle size 2.6
μm Barium sulfate: pH 2.5, average particle size 6.3
μm Barium sulfate: pH 8.2, average particle size 4.5
μm Calcium carbonate: Average particle size 4.9 μm Titanium oxide: Average particle size 0.25 μm

【0015】表1に示した特定の配合量の材料を混練温
度280℃で単軸押出機によりペレットを得、真空乾燥
機(120℃)で24hr乾燥した後、そのMFRを測
定した。また、成形温度280℃で3mm厚板を成形
し、全光線透過率、光拡散透過率を日本電色工業(株)
製のSZ−Σ90で測定した。又、イエローインデック
ス(以下:YI)も日本電色工業(株)製のSZ−Σ9
0の測色計で測定した。YIの測定法は、反射法で標準
白色板を測色面と反対側に置いて測色を行なった。アイ
ゾット衝撃値(表内の記述:Iz値)は、1/4インチ
の試験片でASTM D256に従い値を得た。
Pellets of the materials having the specific compounding amounts shown in Table 1 were obtained by a single screw extruder at a kneading temperature of 280 ° C., dried in a vacuum dryer (120 ° C.) for 24 hours, and then their MFR was measured. Also, a 3 mm thick plate was molded at a molding temperature of 280 ° C., and the total light transmittance and the light diffusion transmittance were measured by Nippon Denshoku Industries Co., Ltd.
It was measured by SZ-Σ90 manufactured by. Also, the yellow index (hereinafter referred to as YI) is SZ-Σ9 manufactured by Nippon Denshoku Industries Co., Ltd.
It was measured with a colorimeter of 0. The YI measurement method was a reflection method in which a standard white plate was placed on the side opposite to the color measurement surface. The Izod impact value (description in the table: Iz value) was obtained according to ASTM D256 on a 1/4 inch test piece.

【0016】[0016]

【表1】 [Table 1]

【0017】[0017]

【表2】 [Table 2]

【0018】表1では、光拡散性ポリカーボネートの例
を示す。その結果、硫酸バリウム及び炭酸カルシウムと
もに同等の全光線透過率と光拡散透過率を得たが、pH
が8.2の硫酸バリウム(比較例2)、炭酸カルシウム
(比較例3)を使用した場合にMFRが高くなってしま
う。また、pH2.5の硫酸バリウム(比較例1)で
は、YIが高くなってしまうことが確認された。
Table 1 shows examples of light diffusing polycarbonates. As a result, the same total light transmittance and light diffusion transmittance were obtained for both barium sulfate and calcium carbonate.
MFR becomes high when barium sulfate (Comparative Example 2) and calcium carbonate (Comparative Example 3) of 8.2 are used. Moreover, it was confirmed that YI was increased with barium sulfate having a pH of 2.5 (Comparative Example 1).

【0019】表2では、光拡散性及び乳白色半透明ポリ
カーボネートの例を示す。その結果、比較例4以外は乳
白色半透明となったが、pH2.5の硫酸バリウム(比
較例4)ではYIが高くなり白色度が損なわれ黄変し乳
白色半透明とならない。また、pH8.2の硫酸バリウ
ム(比較例5)、炭酸カルシウム(比較例6)ではMF
Rが高くなることが確認された。
Table 2 shows examples of light diffusing and milky white translucent polycarbonates. As a result, except for Comparative Example 4, milky white was translucent, but with barium sulfate having a pH of 2.5 (Comparative Example 4), YI was high, whiteness was impaired, and yellowing did not occur, resulting in no milky white translucent. In addition, barium sulfate having a pH of 8.2 (Comparative Example 5) and calcium carbonate (Comparative Example 6) had MF.
It was confirmed that R was high.

【0020】他に炭酸カルシウムを使用した例(比較例
3、6)では顕著にアイゾット衝撃強度(Iz値)が低
下する。沈降性硫酸バリウムを使用することは、ポリカ
ーボネートの物性保持にも有効であることが明らかにな
った。
In addition, in the examples using calcium carbonate (Comparative Examples 3 and 6), the Izod impact strength (Iz value) is remarkably lowered. It was clarified that the use of precipitated barium sulfate is effective for maintaining the physical properties of polycarbonate.

【0021】[0021]

【発明の効果】本発明に係る光拡散性ないしは乳白色半
透明ポリカーボネート樹脂は、全光線透過率が高いにも
かかわらず光拡散性も良好である。それに加えて、ベー
ス樹脂であるポリカーボネート本来の溶融粘度をも低下
させない。したがって、成形の際、粘度低下による成形
不良、例えば成形品のバリ、成形品の金型への噛みつき
による金型の破損等の懸念が全くない光拡散性ないしは
乳白色半透明ポリカーボネート樹脂組成物として幅広い
用途が期待できる。
The light-diffusing or milky white translucent polycarbonate resin according to the present invention has a good light-diffusing property even though the total light transmittance is high. In addition, the original melt viscosity of the base resin, polycarbonate, is not reduced. Therefore, at the time of molding, there is no concern about molding defects due to a decrease in viscosity, for example, burrs of molded products, damage of the mold due to biting of the molded product into the mold, and the like as a light-diffusing or milky white translucent polycarbonate resin composition. Applications can be expected.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】ポリカーボネート樹脂100重量部に対し
て、平均粒子径0.1〜20μm 、pH3.0〜7.5
の範囲にある沈降性硫酸バリウムを0.5〜10重量部
含有せしめたことを特徴とする光拡散性ポリカーボネー
ト樹脂組成物。
1. An average particle diameter of 0.1 to 20 μm and a pH of 3.0 to 7.5 with respect to 100 parts by weight of a polycarbonate resin.
The light-diffusing polycarbonate resin composition is characterized by containing 0.5 to 10 parts by weight of precipitated barium sulfate in the range of 1.
【請求項2】請求項1記載の光拡散性ポリカーボネート
樹脂組成物において、ポリカーボネート樹脂100重量
部に対して、酸化チタンを0.001〜0.2重量部添
加してなる光拡散性及び乳白色半透明ポリカーボネート
樹脂組成物。
2. The light-diffusing polycarbonate resin composition according to claim 1, wherein 0.001 to 0.2 part by weight of titanium oxide is added to 100 parts by weight of the polycarbonate resin. Transparent polycarbonate resin composition.
JP5122038A 1993-04-26 1993-04-26 Light-diffusing polycarbonate resin composition Withdrawn JPH06306266A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5122038A JPH06306266A (en) 1993-04-26 1993-04-26 Light-diffusing polycarbonate resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5122038A JPH06306266A (en) 1993-04-26 1993-04-26 Light-diffusing polycarbonate resin composition

Publications (1)

Publication Number Publication Date
JPH06306266A true JPH06306266A (en) 1994-11-01

Family

ID=14826066

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5122038A Withdrawn JPH06306266A (en) 1993-04-26 1993-04-26 Light-diffusing polycarbonate resin composition

Country Status (1)

Country Link
JP (1) JPH06306266A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000214313A (en) * 1999-01-22 2000-08-04 Elf Atochem Sa Light diffusion composite panel
KR100405320B1 (en) * 2000-12-21 2003-11-12 제일모직주식회사 Polycarbonate Resin Compositions Having Excellent Light Reflectance And Impact-resistance
WO2004034136A1 (en) * 2002-10-03 2004-04-22 General Electric Company Bulk diffuser for flat panel display
CN1318900C (en) * 2003-08-27 2007-05-30 第一毛织株式会社 Light scattering plate and liguid crystal display using the same
US7800714B2 (en) 2005-09-30 2010-09-21 Sharp Kabushiki Kaisha Liquid crystal display and television receiver
US8009248B2 (en) 2005-09-30 2011-08-30 Sharp Kabushiki Kaisha Liquid crystal display and television receiver
US8294736B2 (en) 2006-11-20 2012-10-23 Sharp Kabushiki Kaisha Display device driving method, driving circuit, liquid crystal display device, and television receiver
US8451201B2 (en) 2005-09-30 2013-05-28 Sharp Kabushiki Kaisha Liquid crystal display device drive method, liquid crystal display device, and television receiver
JP2024006512A (en) * 2022-07-04 2024-01-17 株式会社モリシン Method for illuminating printed material, advertisement system, method for manufacturing printed material, and printed material

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000214313A (en) * 1999-01-22 2000-08-04 Elf Atochem Sa Light diffusion composite panel
KR100405320B1 (en) * 2000-12-21 2003-11-12 제일모직주식회사 Polycarbonate Resin Compositions Having Excellent Light Reflectance And Impact-resistance
WO2004034136A1 (en) * 2002-10-03 2004-04-22 General Electric Company Bulk diffuser for flat panel display
US6908202B2 (en) 2002-10-03 2005-06-21 General Electric Company Bulk diffuser for flat panel display
CN1318900C (en) * 2003-08-27 2007-05-30 第一毛织株式会社 Light scattering plate and liguid crystal display using the same
US7800714B2 (en) 2005-09-30 2010-09-21 Sharp Kabushiki Kaisha Liquid crystal display and television receiver
US8009248B2 (en) 2005-09-30 2011-08-30 Sharp Kabushiki Kaisha Liquid crystal display and television receiver
US8451201B2 (en) 2005-09-30 2013-05-28 Sharp Kabushiki Kaisha Liquid crystal display device drive method, liquid crystal display device, and television receiver
US8294736B2 (en) 2006-11-20 2012-10-23 Sharp Kabushiki Kaisha Display device driving method, driving circuit, liquid crystal display device, and television receiver
JP2024006512A (en) * 2022-07-04 2024-01-17 株式会社モリシン Method for illuminating printed material, advertisement system, method for manufacturing printed material, and printed material

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