JPH0618890B2 - Polycarbonate molding material - Google Patents

Polycarbonate molding material

Info

Publication number
JPH0618890B2
JPH0618890B2 JP61146559A JP14655986A JPH0618890B2 JP H0618890 B2 JPH0618890 B2 JP H0618890B2 JP 61146559 A JP61146559 A JP 61146559A JP 14655986 A JP14655986 A JP 14655986A JP H0618890 B2 JPH0618890 B2 JP H0618890B2
Authority
JP
Japan
Prior art keywords
polycarbonate
molding material
powder
less
bis
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.)
Expired - Lifetime
Application number
JP61146559A
Other languages
Japanese (ja)
Other versions
JPS633021A (en
Inventor
征一郎 丸山
博行 河崎
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.)
Mitsubishi Kasei Corp
Original Assignee
Mitsubishi Kasei Corp
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 Mitsubishi Kasei Corp filed Critical Mitsubishi Kasei Corp
Priority to JP61146559A priority Critical patent/JPH0618890B2/en
Publication of JPS633021A publication Critical patent/JPS633021A/en
Publication of JPH0618890B2 publication Critical patent/JPH0618890B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B9/00Making granules
    • B29B9/12Making granules characterised by structure or composition
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2069/00Use of PC, i.e. polycarbonates or derivatives thereof, as moulding material

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Optical Record Carriers And Manufacture Thereof (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明はシルバーの発生の少ない光デイスク用成形材料
に適した低分子量ポリカーボネート成形材料に関するも
のである。
TECHNICAL FIELD The present invention relates to a low molecular weight polycarbonate molding material suitable for a molding material for optical discs, which is less likely to produce silver.

〔従来の技術〕[Conventional technology]

ポリカーボネート樹脂は透明性、耐熱性、低吸水性が優
れているために、光学用途特に最近は光デイスク用成形
材料として使用されはじめた。光デイスクではミクロン
オーダーの信号をレーザー光線で読取り書き込む必要が
あるため、光デイスクの基板中にミクロンオーダー以上
の欠陥があると読み取り、書き込みが出来なくエラーレ
ートの悪化をまねく。このような欠陥としては樹脂の熱
劣化による黒点が有名であるが、それ以外にシルバー
(銀条)といわれる線状欠陥がある。黒点についてはポ
リカーボネート樹脂中に有機亜リン酸エステルを含有さ
せることによる対策が行なわれている(特開昭58−
126119号公報参照)。
Polycarbonate resin is excellent in transparency, heat resistance, and low water absorption, and therefore, it has recently begun to be used as a molding material for optical applications, especially for optical disks. Since it is necessary to read and write signals of micron order with a laser beam in the optical disk, if there is a defect of micron order or more in the substrate of the optical disk, reading and writing cannot be performed and the error rate deteriorates. Black spots due to heat deterioration of the resin are well known as such defects, but there are other linear defects called silver. Regarding black spots, measures have been taken by incorporating an organic phosphite into a polycarbonate resin (JP-A-58-58).
126119).

一方シルバーについては一般に形状も大きいこともあつ
て問題視されてきたが、原因として成形直前ペレツトの
水分の含有率が0.01%以上の乾燥不充分、又は成形
条件の不適正等が考えられ種々の対策がほとんどされて
きた。しかしシルバーによる不良率を1%以下にするこ
とは未だ出来ていないのが現状である。
On the other hand, silver has been regarded as a problem because it generally has a large shape, but the cause is considered to be insufficient drying of the moisture content of the pellet immediately before molding of 0.01% or more, or improper molding conditions. Most of the various measures have been taken. However, the current situation is that it has not been possible to reduce the defective rate due to silver to 1% or less.

〔発明の目的〕[Object of the Invention]

本発明者らは、特に光デイスク基板の成形においてシル
バーの発生を抑制するために、原因検討を行つたとこ
ろ、意外にも粒状体中に粒径1mm以下の微粉が存在する
ことが原因であることを見い出し本発明に到達した。
The inventors of the present invention have conducted a cause investigation to suppress the generation of silver particularly in the molding of an optical disk substrate. Surprisingly, it is caused by the presence of fine powder having a particle diameter of 1 mm or less in the granular body. The present invention has been discovered and the present invention has been reached.

すなわち分子量が10000〜18000のポリカーボネートペレ
ットからなる成形材料であり、該成形材料中における平
均粒径0.5mm以下の粉末状重量体含有量が2.0重量
%以下であり、該粉末状重合体の半径が1mm以下である
ことを特徴とするポリカーボネート成形材料を用いるこ
とでシルバーの発生を抑制できることを見出した。
That is, a molding material composed of polycarbonate pellets having a molecular weight of 10,000 to 18,000, wherein the content of the powdery weight material having an average particle diameter of 0.5 mm or less in the molding material is 2.0% by weight or less, It was found that the generation of silver can be suppressed by using a polycarbonate molding material characterized by having a radius of 1 mm or less.

〔発明の構成〕[Structure of Invention]

以下本発明を具体的に説明する。 The present invention will be specifically described below.

本発明のポリカーボネート樹脂は、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エニル
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
ル交換法によつて得られる重合体または共重合体であ
り、代表的なものとしては、2,2−ビス(4−ヒドロキ
シフエニル)プロパン(ビスフエノールA)から製造さ
れたポリカーボネート樹脂があげられる。
The polycarbonate resin of the present invention is a polymer or copolymer obtained by a phosgene method in which various dihydroxydiaryl compounds are reacted with phosgene, or a transesterification method in which dihydroxydiaryl compounds are reacted with a carbonic acid ester such as diphenyl carbonate. A typical example of the union is a polycarbonate resin produced from 2,2-bis (4-hydroxyphenyl) propane (bisphenol A).

上記ジヒドロキシジアリール化合物としては、ビスフエ
ノールAの他、ビス(4−ヒドロキシフエニル)メタ
ン、1,1−ビス(4−ヒドロキシフエニル)エタン、2,2
−ビス(4−ヒドロキシフエニル)ブタン、2,2−ビス
(4−ヒドロキシフエニル)オクタン、ビス(4−ヒド
ロキシフエニル)フエニルメタン、2,2−ビス(4−ヒ
ドロキシ−3−メチルフエニル)プロパン、1,1−ビス
(4−ヒドロキシ−3−第3ブチルフエニル)プロパ
ン、2,2−ビス(4−ヒドロキシ−3−ブロモフエニ
ル)プロパン、2,2−ビス(4−ヒドロキシ−3,5ジブロ
モフエニル)プロパン、2,2−ビス(4−ヒドロキシ−
3,5ジクロロフエニル)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
シフエニル)シクロペンタン、1,1−ビス(4−ヒドロ
キシフエニル)シクロヘキサンのようなビス(ヒドロキ
シアリール)シクロアルカン酸、4,4′−ジヒドロキシ
ジフエニルエーテル、4,4′−ジヒドロキシ−3,3′−ジ
メチルジフエニルエーテル、のようなジヒドロキシジア
リールエーテル類、4,4′−ジヒドロキシジフエニルス
ルフイド、4,4′−ジヒドロキシ−3,3′−ジメチルジフ
エニルスルフイドのようなジヒドロキシジアリールスル
フイド類、4,4′−ジヒドロキシジフエニルスルホキシ
ド、4,4′−ジヒドロキシ−3,3′−ジメチルジフエニル
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′−ジヒドロキシジフエニルスルホン、4,
4′−ジヒドロキシ−3,3′−ジメチルジフエニルスルホ
ンのようなジヒドロキシジアリールスルホン類等があげ
られる。
Examples of the dihydroxydiaryl compound include bisphenol A, bis (4-hydroxyphenyl) methane, 1,1-bis (4-hydroxyphenyl) ethane, and 2,2
-Bis (4-hydroxyphenyl) butane, 2,2-bis (4-hydroxyphenyl) octane, bis (4-hydroxyphenyl) phenylmethane, 2,2-bis (4-hydroxy-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-3,5dibromophenyl) Enenyl) propane, 2,2-bis (4-hydroxy-
Bis (hydroxyaryl) alkanes such as 3,5 dichlorophenyl) propane, 1,1-bis (4-hydroxyphenyl) cyclopentane, such as 1,1-bis (4-hydroxyphenyl) cyclohexane Dihydroxy diaryl ethers such as bis (hydroxyaryl) cycloalkanoic acid, 4,4'-dihydroxydiphenyl ether, 4,4'-dihydroxy-3,3'-dimethyldiphenyl ether, 4,4'-dihydroxy Diphenyl disulfides such as diphenyl sulfide, 4,4'-dihydroxy-3,3'-dimethyldiphenyl sulfide, 4,4'-dihydroxy diphenyl sulfoxide, 4,4'-dihydroxy Dihydroxydiaryl sulfoxides such as -3,3'-dimethyldiphenyl sulfoxide, 4,4'-dihydroxydiphenyl sulfoxide Sulfone, 4,
Examples thereof include dihydroxydiarylsulfones such as 4'-dihydroxy-3,3'-dimethyldiphenyl sulfone.

これらは単独でまたは2種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′−ジヒドロキシジフエニル等を
混合して使用してもよい。
These may be used alone or in combination of two or more,
In addition to these, piperazine, dipiperidyl, hydroquinone, resorcin, 4,4′-dihydroxydiphenyl and the like may be mixed and used.

光デイスク等の光学用部品には光学的ひずみのないこと
が要求されるので、分子量は10000〜18000、好ましくは
11000〜17000の範囲にする必要がある。なお、ここでい
う分子量(M)はオストワルド粘度計を用い塩化メチレン
を溶媒とする溶液の極限粘度〔η〕を求め、Schnellの
粘度式 〔η〕=1.23×10-5M0.83 から求められる。
Since optical components such as optical discs are required to have no optical distortion, the molecular weight is 10,000 to 18,000, preferably
Must be in the range 11000-17000. The molecular weight (M) as used herein is determined from the Schnell's viscosity formula [η] = 1.23 × 10 -5 M 0.83 by determining the intrinsic viscosity [η] of a solution using methylene chloride as a solvent using an Ostwald viscometer.

光デイスク等の光学用部品用のポリカーボネート成形材
料には低粘度のものが使用されるので、成形機のスクリ
ユーによるせん断発熱が少なく、通常2〜4mmの粒径の
粒状体(ペレツト)中の1mm径以下の微粉の重合体はシ
リンダーからの熱でしか溶融されない。しかしポリカー
ボネートなどの重合体の熱伝導性は低いので、微粉の重
合体は未溶融状態で射出成形され、成形品中にシルバー
状欠陥として観察される。したがつて粉末状重合体の含
有量が2.0重量%より多いと未溶融粉末となる可能性
が大きくシルバーの発生が多く、2.0重量%以下、好
ましくは1.0重量%以下ならばシルバーによる不良率
を1〜2%以下におさえられ、光学用途としても要求さ
れる目標が達成される。
Polycarbonate molding materials for optical parts such as optical discs have low viscosity, so there is little shear heat generation by the screen of the molding machine, and it is usually 1 mm in granules (pellets) with a particle size of 2-4 mm. A finely divided polymer having a diameter not larger than that can be melted only by heat from the cylinder. However, since a polymer such as polycarbonate has a low thermal conductivity, a finely divided polymer is injection-molded in an unmelted state and is observed as a silver-like defect in a molded product. Therefore, if the content of the powdery polymer is more than 2.0% by weight, unmelted powder is likely to occur and silver is often generated. If 2.0% by weight or less, preferably 1.0% by weight or less, For example, the defective rate due to silver can be suppressed to 1 to 2% or less, and the target required for optical applications can be achieved.

本発明のポリカーボネート成形材料において、平均粒径
が0.5mm以下のポリカーボネート粉末含有量を2%以
下にするためには、溶融ポリマーを冷却してペレツト化
するカツテイング工程でのカツテイング条件を最適化し
粉末発生量を極小化すること、ペレツト化以降について
も全工程にわたりペレツトに加わる機械的剪断力をでき
るだけ小さくし粉末の発生を極力抑える必要がある。特
に乾燥工程、配合工程、包装工程などの各工程、および
これら工程間を結ぶ空送等のペレツト輸送工程における
ペレツト同志、ペレツトと装置器壁との衝突を極小化
し、またすべての単位操作において回転式撹拌機などの
強度の剪断履歴を与える手段を用いないことが重要であ
る。本発明で使用するような10,000〜18,000の比較的低
分子量のポリカーボネートは強度が弱くなるためペレツ
ト化するカツテイング工程において粉末が発生しやす
い。従つてペレツト化時のカツター刃の摩耗、ストラン
ドの温度などが粉末の発生に大きな要因となる。また製
造工程において不可避的に発生したポリカーボネート粉
末については、製造工程の最終段階において該粉末を低
減せしめることも可能である。粉末除去の方法としては
振動篩など機械的方法がよく知られている。ただしペレ
ツト表面に付着した微細な粉末は機械的方法では満足に
除去し難く、また水洗等の特殊な粉末除去を行なうとき
は、工程の煩雑化、生産能率の低下を招く。したがつて
製造工程で粉末の発生量を極小化し、さらに最終工程で
粉末量を低減することがより好ましい。
In the polycarbonate molding material of the present invention, in order to reduce the content of the polycarbonate powder having an average particle diameter of 0.5 mm or less to 2% or less, the cutting conditions in the cutting process of cooling the molten polymer into pellets are optimized to obtain powder. It is necessary to minimize the amount of generation and to suppress the generation of powder as much as possible even after pelletization, by reducing the mechanical shearing force applied to the pellet as much as possible throughout the entire process. In particular, it minimizes collisions between pellets, pellets in the pellet transporting process such as drying process, compounding process, packaging process, and pellet transporting process connecting these processes, and rotation in all unit operations. It is important not to use means such as a mechanical stirrer to provide a strong shear history. Since the polycarbonate having a relatively low molecular weight of 10,000 to 18,000 as used in the present invention has low strength, powder is likely to be generated in the cutting process for pelletizing. Therefore, wear of the cutter blade during pelletization, temperature of the strand, etc. are major factors in the generation of powder. Further, regarding the polycarbonate powder which is inevitably generated in the manufacturing process, it is possible to reduce the powder at the final stage of the manufacturing process. A mechanical method such as a vibrating screen is well known as a method for removing powder. However, it is difficult to satisfactorily remove the fine powder adhering to the pellet surface by a mechanical method, and when performing special powder removal such as washing with water, the process becomes complicated and the production efficiency is lowered. Therefore, it is more preferable to minimize the amount of powder generated in the manufacturing process and further reduce the amount of powder in the final process.

本発明におけるポリカーボネートペレツト中の全粉末量
の測定は、次の方法により行なう。ポリカーボネートペ
レツト100〜200gを秤量した後、30メツシユの
ステンレス金網容器に入れ、300〜400ccのメタノ
ール中でよく振盪してペレツトを洗浄し、粉末をメタノ
ール中に分離せしめる。ここで分離される粉末は通常粒
径1mm以下である。
The total amount of powder in the polycarbonate pellet of the present invention is measured by the following method. After weighing 100 to 200 g of polycarbonate pellets, the pellets are placed in a stainless steel mesh container of 30 mesh and shaken well in 300 to 400 cc of methanol to wash the pellets, and the powder is separated in methanol. The powder separated here usually has a particle size of 1 mm or less.

この洗浄液をG4ガラスフイルターで別する。この操
作をメタノール中に浮遊物が認められなくなるまで繰り
返す。通常4〜5回の操作で取された残渣の重量は恒
量に達する。この残渣の重量を粉末重量とする。
Separate this wash with a G4 glass filter. This operation is repeated until no suspended substance is observed in methanol. Usually, the weight of the residue taken in 4 to 5 times reaches a constant weight. The weight of this residue is the powder weight.

以上はペレツトに添加剤が表面添着されていない場合で
あるが、通常ポリカーボネートは添加剤が全て練込まれ
ていることが多く、特に光デイスクなどのように成形室
のクリーン度をクラス1000以下に保持するには添加
剤が全て練込まれている方が好ましい。添加剤が表面添
着されている場合には、メタノール中に添加剤も移行す
るため添加剤の定性、定量を行なわなければならない。
分析の具体的方法については添加剤の種類によりそれぞ
れ異なるので個々の添加剤について各々最適の定量方法
を選定すればよい。
The above is the case where the additive is not surface-adhered to the pellet, but usually the additive is often mixed in polycarbonate, and especially the cleanliness of the molding chamber, such as optical disk, is set to class 1000 or less. In order to keep it, it is preferable that all the additives are kneaded. When the additive is surface-attached, the additive also migrates into methanol, so the additive must be qualitatively and quantitatively determined.
Since the specific method of analysis differs depending on the type of additive, it is only necessary to select the optimum quantification method for each additive.

ポリカーボネートペレツトは通常2.0〜3.5mm径の
球状又は直径および長さが2.0〜4.0mmの円柱の粒
状体になつており、直径又は長さが2.0mm以上ならば
形状は特に問題ではない。
Polycarbonate pellets are usually spherical particles with a diameter of 2.0 to 3.5 mm or cylindrical granules with a diameter and length of 2.0 to 4.0 mm. If the diameter or length is 2.0 mm or more, the shape is Is not particularly a problem.

粉末の平均粒径の測定は前述のようにして採集した粒径
1mm以下の粉末を光学顕微鏡を用い、視野内の200〜
1000個の粉末粒子について粒子の最大幅(粒子の投
影像をその面内の二平行線によつて挾むときその距離の
最大のもの)を測定し、算術平均をとつたものとする。
To measure the average particle size of the powder, the powder having a particle size of 1 mm or less collected as described above is used in the visual field of 200 to
The maximum width of the particles (the maximum distance when the projected image of the particles is sandwiched by the two parallel lines in the plane) is measured for 1000 powder particles, and the arithmetic mean is taken.

本発明の成形材料はスクリユー等の剪断力で可塑化する
成形機、すなわち射出成形機、射出圧縮成形機、押出成
形機において有効で、デイスク、レンズ、ミラー、銘
板、シート、プレートなどの種々のものに加工される。
INDUSTRIAL APPLICABILITY The molding material of the present invention is effective in a molding machine that is plasticized by a shearing force such as a screw, that is, an injection molding machine, an injection compression molding machine, an extrusion molding machine, and can be used in various materials such as a disk, a lens, a mirror, a nameplate, a sheet, and a plate. Processed into a thing.

〔実施例〕 以下本発明について実施例により更に詳しく説明する
が、本発明はこれらの実施例に限定されるものではな
い。
[Examples] Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited to these Examples.

実施例1、2、比較例1 常法によりビスフエノールAとホスゲンを界面重合法で
重合して、得られた分子量15000のポリカーボネート粉
末に、有機亜リン酸エステル(トリスノニルフエニルフ
オスフアイト、アデカアーガス社製 Mark1178)を0.
05%をブレンド后、40mmφベント押出機にて250
℃でストランド状に押出し、ペレツト化のためカツテイ
ングし、2.5mm径、3.0mm長さの円柱状ペレツトを
得た。この粒状体を前述に記載の方法で粉末状重合体の
平均粒径及び含有量の測定をした。結果はそれぞれ0.
41mm、2.8重量%であつた。このペレツトをさらに
振動ぶるいあるいは水洗することにより表−1に示すよ
うな粉末を含有するペレツトを得た。
Examples 1, 2 and Comparative Example 1 Bisphenol A and phosgene were polymerized by an interfacial polymerization method by a conventional method to obtain a polycarbonate powder having a molecular weight of 15,000 and organic phosphite (trisnonylphenylphosphite, ADEKA Mark 1178 made by Argus Co., Ltd.
After blending 05%, use a 40mmφ vent extruder to 250
It was extruded in a strand form at ℃ and cut for pelletization to obtain a cylindrical pellet having a diameter of 2.5 mm and a length of 3.0 mm. The average particle size and content of the powdery polymer of this granular material were measured by the method described above. The results are 0.
It was 41 mm and 2.8% by weight. The pellet was further shaken by shaking or washed with water to obtain a pellet containing powder as shown in Table 1.

これらペレツトをカールフイツシヤー法による水分含有
率が50ppmになるまで乾燥して、射出成形機(名機製
M−100DM)で120mm径、1.2mm厚みのコンパク
トデイスクの成形を実施した。条件は樹脂温度340
℃、金型温度95℃、射出率105cc/secの射出スピ
ードであつた。
These pellets were dried by the Karl Fisher method until the water content became 50 ppm, and a 120 mm diameter, 1.2 mm thick compact disk was molded by an injection molding machine (M-100DM manufactured by Meiki). Conditions are resin temperature 340
C., mold temperature 95.degree. C., injection rate 105 cc / sec.

このコンパクトデイスクを連続して200枚成形し、シ
ルバーの発生したデイスクを目視で観察し、その枚数を
測定し、そのシルバー発生デイスクの比率を不良率とし
て測定した。結果を表−1に示す。
200 sheets of this compact disk were continuously molded, the disks in which silver was generated were visually observed, the number of disks was measured, and the ratio of the disks in which silver was generated was measured as a defective rate. The results are shown in Table-1.

これより、微粉が少なくなれば急激にシルバーの発生が
少なくなることが示される。
From this, it is shown that the generation of silver decreases sharply as the amount of fine powder decreases.

〔発明の効果〕 本発明による成形材料は、シルバーの発生を防止でき、
不良率を著しく低下出来るため商業上の利用価値は極め
て高い。
[Effect of the Invention] The molding material according to the present invention can prevent the generation of silver,
The utility value is extremely high because the defect rate can be significantly reduced.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】分子量が10000〜18000のポリカ
ーボネートペレットからなる成形材料であり、該成形材
料中における平均粒径0.5mm以下の粉末状重合体含有
量が2.0重量%以下であることを特徴とするポリカー
ボネート成形材料。
1. A molding material comprising polycarbonate pellets having a molecular weight of 10,000 to 18,000, wherein the content of the powdery polymer having an average particle diameter of 0.5 mm or less in the molding material is 2.0% by weight or less. Characteristic polycarbonate molding material.
【請求項2】ポリカーボネートペレットが実質的に粒径
2mm以上の粒状体である特許請求の範囲第1項記載のポ
リカーボネート成形材料。
2. The polycarbonate molding material according to claim 1, wherein the polycarbonate pellet is a granular body having a particle size of substantially 2 mm or more.
【請求項3】粉末状重合体が粒径1mm以下であることを
特徴とする特許請求の範囲第1項記載のポリカーボネー
ト成形材料。
3. The polycarbonate molding material according to claim 1, wherein the powdery polymer has a particle diameter of 1 mm or less.
JP61146559A 1986-06-23 1986-06-23 Polycarbonate molding material Expired - Lifetime JPH0618890B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61146559A JPH0618890B2 (en) 1986-06-23 1986-06-23 Polycarbonate molding material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61146559A JPH0618890B2 (en) 1986-06-23 1986-06-23 Polycarbonate molding material

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP6797595A Division JPH07324138A (en) 1995-03-27 1995-03-27 Method of molding optical component

Publications (2)

Publication Number Publication Date
JPS633021A JPS633021A (en) 1988-01-08
JPH0618890B2 true JPH0618890B2 (en) 1994-03-16

Family

ID=15410409

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61146559A Expired - Lifetime JPH0618890B2 (en) 1986-06-23 1986-06-23 Polycarbonate molding material

Country Status (1)

Country Link
JP (1) JPH0618890B2 (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5187256A (en) * 1990-12-03 1993-02-16 The Dow Chemical Company Uniform distribution polycarbonate pellet
JP3611950B2 (en) * 1997-07-23 2005-01-19 三菱エンジニアリングプラスチックス株式会社 Polycarbonate molding material for optical disk substrate
KR20010040764A (en) * 1998-02-09 2001-05-15 빌프리더 하이더 Polymer Particles
JPH11342510A (en) * 1998-04-03 1999-12-14 Teijin Chem Ltd Optical molding material
EP1236758B1 (en) 2000-04-28 2006-08-23 Teijin Chemicals, Ltd. Colored master pellet for optical moldings and colored optical disk substrate
US6858298B2 (en) 2001-03-07 2005-02-22 Teijin Chemicals, Ltd. Optical polycarbonate resin molding material
US6833427B2 (en) 2001-05-18 2004-12-21 Teijin Chemicals, Ltd. Polycarbonate resin molding material for optical use
JP4691844B2 (en) * 2001-07-11 2011-06-01 Jsr株式会社 Molding material and molded product
JP6982398B2 (en) * 2016-04-15 2021-12-17 ポリプラスチックス株式会社 Polybutylene terephthalate resin composition and molded products using it

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54127463A (en) * 1978-03-13 1979-10-03 Du Pont Melting cutter apparatus
JPS5749515A (en) * 1980-09-09 1982-03-23 Mitsubishi Rayon Co Ltd Manufacture of pellet
JPS58126119A (en) * 1982-01-22 1983-07-27 Mitsubishi Chem Ind Ltd Manufacture of molding excellent in optical property

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54127463A (en) * 1978-03-13 1979-10-03 Du Pont Melting cutter apparatus
JPS5749515A (en) * 1980-09-09 1982-03-23 Mitsubishi Rayon Co Ltd Manufacture of pellet
JPS58126119A (en) * 1982-01-22 1983-07-27 Mitsubishi Chem Ind Ltd Manufacture of molding excellent in optical property

Also Published As

Publication number Publication date
JPS633021A (en) 1988-01-08

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