JPS6210160A - Material for optical instrument - Google Patents
Material for optical instrumentInfo
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- JPS6210160A JPS6210160A JP60148317A JP14831785A JPS6210160A JP S6210160 A JPS6210160 A JP S6210160A JP 60148317 A JP60148317 A JP 60148317A JP 14831785 A JP14831785 A JP 14831785A JP S6210160 A JPS6210160 A JP S6210160A
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Abstract
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は光学機器用素材に関し、特に耐熱性。[Detailed description of the invention] [Industrial application field] The present invention relates to materials for optical equipment, particularly heat resistance.
成形加工性にすぐれ、デジタルオーディオディスクや光
メモリ−ディスクなどに適した素材に関する。It relates to a material that has excellent moldability and is suitable for digital audio discs, optical memory discs, etc.
〔従来の技術及び発明が解決しようとする問題点〕一般
に、上述したような光学機器用の素材には様々な性能が
要求されている。例えば、透明性。[Prior Art and Problems to be Solved by the Invention] In general, materials for optical devices such as those described above are required to have various performances. For example, transparency.
耐熱性、低透湿性2機械的強度等に優れているとともに
光学的性質に優れていることが必要である。It is necessary to have excellent heat resistance, low moisture permeability, mechanical strength, etc., as well as excellent optical properties.
従来、このような性質を有するものの一つとして、メタ
クリル樹脂が知られているが、このものは耐熱性や低透
湿性、耐衝撃性などの点において未だ充分なものとは言
い難いという欠点がある。Conventionally, methacrylic resin has been known as one of the materials having such properties, but this resin has the disadvantage that it is still difficult to say that it is sufficient in terms of heat resistance, low moisture permeability, impact resistance, etc. be.
また、ビスフェノールA(2,2−ビス(4°−ヒドロ
キシフェニル)プロパン)をホスゲンや炭酸ジフェニル
等と反応させて得られるポリカーボネート樹脂が光学機
器用素材として使用しうろことも知られているが、この
ものは耐熱性、低透湿性、耐衝撃性などにおいて優れて
いるものの、光弾性係数が比較的大きく、しかも成形加
工時の流動性を示す流れ値が小さい。そのため成形加工
後の残留応力による成形品の歪みが大きく、これらに基
因して成形品の複屈折が大きくなり、ディスとして充分
に満足すべきものは得られていない。It is also known that polycarbonate resin obtained by reacting bisphenol A (2,2-bis(4°-hydroxyphenyl)propane) with phosgene, diphenyl carbonate, etc. can be used as a material for optical equipment. Although this material has excellent heat resistance, low moisture permeability, and impact resistance, it has a relatively large photoelastic coefficient and a low flow value, which indicates fluidity during molding. Therefore, the distortion of the molded product due to residual stress after the molding process is large, and due to these, the birefringence of the molded product becomes large, and a fully satisfactory disk cannot be obtained.
そこで本発明者らは耐熱性2機械的強度などポリカーボ
ネート樹脂の有する優れた特性を維持するとともに、特
にポリカーボネート樹脂の欠点である流動性、光弾性係
数などを改善することによって、光学的性質の向上した
素材を開発するために鋭意研究を重ねた。Therefore, the present inventors maintained the excellent properties of polycarbonate resin such as heat resistance 2 and mechanical strength, and in particular improved the disadvantages of polycarbonate resin such as fluidity and photoelastic coefficient, thereby improving optical properties. In order to develop this material, we conducted extensive research.
その結果、特定の繰返し単位を有する二種類のポリカー
ボネート系の重合体を配合してなる組成物が上記目的を
達成しうるものであることを見出し、この知見に基いて
本発明を完成するに至った。As a result, it was discovered that a composition formed by blending two types of polycarbonate polymers having specific repeating units could achieve the above object, and based on this knowledge, the present invention was completed. Ta.
すなわち本発明は、
一般式
〔式中、R’、Rtはそれぞれ炭素数1〜5のアルキル
基あるいはフェニル基を示し、Xl、xZはそれぞれ炭
素数1〜4のアルキル基、炭素数1〜4のアルコキシル
基あるいはハロゲン原子を示す。〕で表わされる繰返し
単位を有する重合体〔A31〜99重量%および
一般式
〔式中、Rt R4はそれぞれ炭素数1〜5のアルキル
基あるいはフェニル基を示す。〕
で表わされる繰返し単位を有する重合体〔B〕99〜1
重量%を配合した組成物からなる光学機器用素材を提供
するもである。That is, the present invention is based on the general formula [wherein R' and Rt each represent an alkyl group having 1 to 5 carbon atoms or a phenyl group, and Xl and xZ each represent an alkyl group having 1 to 4 carbon atoms, and 1 to 4 carbon atoms] represents an alkoxyl group or a halogen atom. A polymer having repeating units represented by [A31 to 99% by weight] and the general formula [wherein Rt R4 represents an alkyl group having 1 to 5 carbon atoms or a phenyl group, respectively]. ] Polymer [B] 99-1 having a repeating unit represented by
The object of the present invention is to provide a material for optical equipment comprising a composition containing % by weight.
上記一般式CI)で表わされる繰返し単位を有する重合
体〔A〕は、R1,R2および)(+、x2の種類によ
り様々なものがあるが、これらの具体例を示せば、R1
,R2はメチル基、エチル基、 n −プロピル基、
i−プロピル基、n−ブチル基、i−ブチル基、 5e
c−ブチル基、 tert−ブチル基。The polymer [A] having a repeating unit represented by the general formula CI) has various types depending on the types of R1, R2 and )(+, x2. Specific examples thereof include R1
, R2 is a methyl group, an ethyl group, an n-propyl group,
i-propyl group, n-butyl group, i-butyl group, 5e
c-butyl group, tert-butyl group.
n−アミル基、i−アミル基、 5ec−アミル基。n-amyl group, i-amyl group, 5ec-amyl group.
tert−アミル基あるいはフェニル基などである。Examples include tert-amyl group and phenyl group.
ここでR1,R1は同じものであってもよく、異なるも
のであってもよい。また、xl、xtの具体例としては
、メチル基、エチル基、n−プロピル基。Here, R1 and R1 may be the same or different. Further, specific examples of xl and xt include a methyl group, an ethyl group, and an n-propyl group.
i−プロピル基、n−ブチル基、i−ブチル基。i-propyl group, n-butyl group, i-butyl group.
5ec−ブチル基、 tert−ブチル基あるいはメト
キシル基、エトキシル基、n−プロポキシル基、i−プ
ロポキシル基、n−ブトキシル基、i−ブトキシル基I
5ec−ブトキシル基、 tert−ブトキシル基、
さらには塩素、臭素、沃素をあげることができる。この
)(1,xlについても共に同じであっても異なるもの
であってもよい。5ec-butyl group, tert-butyl group or methoxyl group, ethoxyl group, n-propoxyl group, i-propoxyl group, n-butoxyl group, i-butoxyl group I
5ec-butoxyl group, tert-butoxyl group,
Further examples include chlorine, bromine, and iodine. )(1 and xl may also be the same or different.
上記重合体〔A〕の重合度は、光学機器の種類や重合体
〔A〕、〔B〕よりなる組成物中の再重合体の配合割合
等に応じて適宜定めればよいが、この重合度を示す粘度
が、25℃における濃度0.5g/aの塩化メチレン溶
液の還元粘度〔η1/c〕として0.3〜1.0 dl
/ g、好マシくは0.35〜0.8d17gの重合体
になるように重合させるべきである。The degree of polymerization of the above polymer [A] may be determined as appropriate depending on the type of optical equipment and the blending ratio of the repolymer in the composition consisting of polymers [A] and [B]. The reduced viscosity [η1/c] of a methylene chloride solution with a concentration of 0.5 g/a at 25°C is 0.3 to 1.0 dl.
/g, preferably 0.35-0.8d17g of polymer.
一方、前述の一般式(n)で表わされる繰返し単位を有
する重合体〔B〕は、R3,R4の種類により様々なも
のがある。このR3,R4の具体例としては、上述のR
1,R2の場合と同じものがあげられる。但し、R:l
、R4は必ずしも同一であることは要せず、互いに異な
るものであってもよい。On the other hand, there are various polymers [B] having repeating units represented by the above-mentioned general formula (n) depending on the types of R3 and R4. As a specific example of R3 and R4, the above-mentioned R
The same thing as in the case of 1 and R2 can be mentioned. However, R:l
, R4 do not necessarily have to be the same, and may be different from each other.
また、この重合体〔B〕の重合度は、前述の重合体〔A
〕の場合と同様に、様々な状況に応じて適宜定めればよ
いが、゛この重合度を示す粘度が、25℃における濃度
0.5g/dIの塩化メチレン溶液の還元粘度〔η1/
C〕として0.3〜1.0di/g、好ましくは0.3
5〜0.8aJ/gの重合体となるように重合させるべ
きである。Moreover, the degree of polymerization of this polymer [B] is the same as that of the above-mentioned polymer [A].
], the viscosity indicating the degree of polymerization is the reduced viscosity of a methylene chloride solution with a concentration of 0.5 g/dI at 25°C [η1/
C] from 0.3 to 1.0 di/g, preferably 0.3
The polymerization should be between 5 and 0.8 aJ/g of polymer.
本発明における組成物は、前述した重合体〔A〕と重合
体〔B〕よりなるものであるが、両者の配合割合は重合
体〔A〕 1〜99重量%、重合体〔B〕99〜1重量
%の範囲で適宜選定すればよい。特にそのうち、重合体
〔A〕を80〜99重量%、重合体〔B〕を20〜1重
量%の範囲に定めることが、光弾性係数の小さい素材を
得る上で好都合である。The composition in the present invention is composed of the above-mentioned polymer [A] and polymer [B], and the blending ratio of both is 1 to 99% by weight for polymer [A] and 99 to 99% by weight for polymer [B]. It may be appropriately selected within the range of 1% by weight. In particular, it is convenient to set the polymer [A] to 80 to 99% by weight and the polymer [B] to 20 to 1% by weight in order to obtain a material with a small photoelastic coefficient.
なお、上述の重合体〔A〕、〔B〕は様々な方法により
製造することができるが、通常はビスフェノールAを出
発原料とする一般のポリカーボネート樹脂と同様に製造
することができる。例えば、重合体〔A〕を製造するに
は、
一般式
〔式中、R1,R2およびxl、x2は前記と同じ。〕
で表わされるビスフェノール類にホスゲンを加え、適当
な溶媒中でアルカリや所望により分子量調節剤等の存在
下にて反応させるホスゲン法によることができる。また
、ホスゲンの代わりに炭酸ジフェニル等を用いるエステ
ル交換法によっても製造することができる。一方、重合
体〔B〕は原料としてのビスフェノール類として
一般式
(R3,R4は前記と同じ。)
で表わされるものを用い、他は上述した重合体〔A〕の
製造法と同様にして製造することができる。Although the above-mentioned polymers [A] and [B] can be produced by various methods, they can usually be produced in the same manner as general polycarbonate resins using bisphenol A as a starting material. For example, to produce the polymer [A], the general formula [wherein R1, R2, xl, and x2 are the same as above] is used. ]
The phosgene method can be used, in which phosgene is added to bisphenols represented by and reacted in an appropriate solvent in the presence of an alkali and, if desired, a molecular weight regulator. It can also be produced by a transesterification method using diphenyl carbonate or the like instead of phosgene. On the other hand, polymer [B] is produced using bisphenols represented by the general formula (R3 and R4 are the same as above) as raw materials, and in the same manner as the production method of polymer [A] described above. can do.
本発明における組成物は、上記重合体〔A〕と重合体C
B)を所定割合で配合すれば得られるが、一般にはこれ
らの重合体〔A〕、 〔B〕を適当な溶剤、例えば塩
化メチレン、テトラクロルエタン。The composition in the present invention comprises the above polymer [A] and polymer C.
It can be obtained by blending B) in a predetermined ratio, but generally these polymers [A] and [B] are mixed in a suitable solvent such as methylene chloride or tetrachloroethane.
クロルフェノール等のハロゲン化炭化水素に溶解させて
充分に混合した後、この溶剤を減圧除去等の適当な手段
で除去することによって得る。It is obtained by dissolving it in a halogenated hydrocarbon such as chlorophenol and thoroughly mixing it, and then removing the solvent by an appropriate means such as removal under reduced pressure.
なお、この組成物を用いてディスク等を成形するにあた
っては、酸化防止剤、紫外線吸収剤などの通常の添加剤
を配合してもよい。In addition, when molding a disk or the like using this composition, usual additives such as antioxidants and ultraviolet absorbers may be added.
このようにして得られる本発明の組成物は、従来のポリ
カーボネート樹脂に比べて光弾性係数が小さく、また成
形性が良好であって成形歪が少ないため複屈折が小さく
光学的性質の極めてすぐれたものである。しかも、耐熱
性2機械的強度にもすぐれたものである。したがって本
発明の組成物を各種光学機器の素材として用いれば光学
的性質が改良されているためディスクに記録された情報
の読取り感度が高く、エラーの発生の少ない光学機器が
得られる。また、熱的にも機械的にも良好な素材である
ため、これを用いて作られた光学機器は様々な条件下で
安定して作動する。The composition of the present invention obtained in this way has a smaller photoelastic coefficient than conventional polycarbonate resins, has good moldability, and has little molding distortion, so it has low birefringence and extremely excellent optical properties. It is something. Moreover, it has excellent heat resistance and mechanical strength. Therefore, if the composition of the present invention is used as a material for various optical devices, it will be possible to obtain optical devices that have improved optical properties, have high sensitivity in reading information recorded on disks, and are less prone to errors. Additionally, since it is a material that is good both thermally and mechanically, optical devices made using it operate stably under a variety of conditions.
それ故、本発明の素材は、デジタルオーディオディスク
や光メモリ−ディスクなどの光学機器用素材として有効
に利用することができる。Therefore, the material of the present invention can be effectively used as a material for optical equipment such as digital audio discs and optical memory discs.
次に、本発明を実施例によりさらに詳しく説明する。 Next, the present invention will be explained in more detail with reference to Examples.
実施例1
11t容のフラスコに、2,2−ビス(3゛−メチル−
41−ヒドロキシフェニル)プロパン25.6g(0,
1モル)を2規定の水酸化ナトリウム水溶液250nl
に溶解した溶液と、塩化メチレン250m1.分子量調
節剤としてのp−ターシャリ−ブチルフェノール0.2
gならびに触媒としてのトリエチルアミン0.5mj!
を加え、激しく撹拌しながら、ホスゲンを300mj!
/分の割合で吹き込み、フラスコ内のpHが9になった
時点でホスゲンガスの供給を停止した。その後、1時間
攪拌しながら反応を行った。反応終了後、反応生成物を
塩化メチレン200m1で希釈した後、水、0.01規
定の塩酸および水の順序で洗浄し、有機層を分離してメ
タノール中に投入し、下記の式で示される繰返し単位(
I[[)を存するポリカーボネート(重合体〔A〕)を
得た。Example 1 2,2-bis(3'-methyl-
41-hydroxyphenyl)propane 25.6 g (0,
1 mol) in 250 nl of 2N aqueous sodium hydroxide solution
of methylene chloride and 250 ml of methylene chloride. p-tert-butylphenol as molecular weight regulator 0.2
g and 0.5 mj of triethylamine as a catalyst!
and while stirring vigorously, add 300 mj of phosgene!
The supply of phosgene gas was stopped when the pH inside the flask reached 9. Thereafter, the reaction was carried out with stirring for 1 hour. After the reaction was completed, the reaction product was diluted with 200ml of methylene chloride, washed in the order of water, 0.01N hydrochloric acid, and water, and the organic layer was separated and poured into methanol to form a product represented by the following formula. Repeat unit (
A polycarbonate (polymer [A]) containing I[[] was obtained.
この重合体〔A〕は塩化メチレンを溶媒とする濃度0.
5g/aの溶液25℃における還元粘度〔ηsp/c)
が0.834/gであった。This polymer [A] has a concentration of 0.
Reduced viscosity of 5g/a solution at 25°C [ηsp/c)
was 0.834/g.
上記の重合体〔A〕4.75gおよび下記式で示される
繰返し単位(IV)
を有する市販のポリカーボネート(重合体〔B〕)(上
記の条件下で測定した還元粘度0.5d!/g)0、.
25 gを、塩化メチレン200m6中に完全に溶解し
た後、溶媒の塩化メチレンを減圧下に除去してポリカー
ボネート組成物を得た。このようにして得られた組成物
を270℃において熱プレスすることにより、肉厚9.
3mmのシートを得た。Commercially available polycarbonate (polymer [B]) having 4.75 g of the above polymer [A] and a repeating unit (IV) represented by the following formula (reduced viscosity measured under the above conditions: 0.5 d!/g) 0,.
After completely dissolving 25 g in 200 m6 of methylene chloride, the solvent methylene chloride was removed under reduced pressure to obtain a polycarbonate composition. By hot pressing the composition thus obtained at 270°C, the thickness of the composition was 9.
A 3 mm sheet was obtained.
このシートを用い波長633nmにおける光弾性係数を
測定した。またこのもののガラス転移温度を測定して耐
熱性を評価した。これらの結果を第1表に示す。Using this sheet, the photoelastic coefficient at a wavelength of 633 nm was measured. The glass transition temperature of this material was also measured to evaluate its heat resistance. These results are shown in Table 1.
実施例2
実施例1において、塩化メチレンに溶解する重合体〔A
〕を4.5g、重合体CB)を0.5gとしたこと以外
は、実施例1と同様の操作を行なった。結果を第1表に
示す。Example 2 In Example 1, the polymer [A
] was changed to 4.5 g, and polymer CB) was changed to 0.5 g, but the same operation as in Example 1 was performed. The results are shown in Table 1.
実施例3
実施例1において、塩化メチレンに溶解する重合体〔A
〕を4.0g、重合体〔B〕を1.0gとしたこと以外
は、実施例1と同様の操作を行なった。結果を第1表に
示す。Example 3 In Example 1, polymer [A
] was changed to 4.0 g, and the same operation as in Example 1 was performed, except that the amount of polymer [B] was changed to 1.0 g. The results are shown in Table 1.
実施例4
実施例1において、塩化メチレンに溶解する重合体〔A
〕を0.5g、重合体〔B〕を4.5gとしたこと以外
は、実施例1と同様の操作を行なった。結果を第1表に
示す。Example 4 In Example 1, the polymer [A
] was changed to 0.5 g, and the polymer [B] was changed to 4.5 g, but the same operation as in Example 1 was performed. The results are shown in Table 1.
実施例5
実施例1において、2,2−ビス(3°−メチ/L/−
4’−ヒドロキシフェニル)プロパンに代えて3,3−
ビス(3°−メチル−4°−ヒドロキシフェニル)ペン
タン28.4 g (0,1モル)ヲ用いたこと以外は
実施例1と同様の反応を行なって、下記式で示される繰
返し単位(V)を有するポリカーボネート(重合体〔A
〕)を得た。Example 5 In Example 1, 2,2-bis(3°-methy/L/-
3,3- instead of 4'-hydroxyphenyl)propane
The same reaction as in Example 1 was carried out except that 28.4 g (0.1 mol) of bis(3°-methyl-4°-hydroxyphenyl)pentane was used, and the repeating unit (V ) having polycarbonate (polymer [A
]) was obtained.
この重合体〔A〕の実施例1と同じ条件下で測定した還
元粘度〔η、、/ C)は0.75d1/gであった。The reduced viscosity [η, /C) of this polymer [A] measured under the same conditions as in Example 1 was 0.75 d1/g.
上記の重合体〔A〕 4.75 gど実施例1と同じ重
合体〔B〕0.25gを塩化メチレン200m1中に完
全に溶解し、以降は実施例1と同様の操作を行なってシ
ートを得、各種物性を測定した。結果を第1表に示す。Completely dissolve 4.75 g of the above polymer [A] and 0.25 g of the same polymer [B] as in Example 1 in 200 ml of methylene chloride, and then perform the same operations as in Example 1 to form a sheet. and various physical properties were measured. The results are shown in Table 1.
実施例6
実施例5において塩化メチレンに溶解する重合体〔A〕
を4.5g、重合体CB)を0.5gとしたこと以外は
、実施例5と同様の操作を行なった。Example 6 Polymer [A] dissolved in methylene chloride in Example 5
The same operation as in Example 5 was performed except that the amount of polymer CB) was 4.5 g and the amount of polymer CB) was 0.5 g.
結果を第1表に示す。The results are shown in Table 1.
比較例1
実施例1に用いた繰返し単位(IV)を有する市販のポ
リカーボネート(重合体〔B〕)の各種物性を第1表に
示す。Comparative Example 1 Table 1 shows various physical properties of the commercially available polycarbonate (polymer [B]) having the repeating unit (IV) used in Example 1.
Claims (4)
キル基あるいはフェニル基を示し、X^1、X^2はそ
れぞれ炭素数1〜4のアルキル基、炭素数1〜4のアル
コキシル基あるいはハロゲン原子を示す。〕で表わされ
る繰返し単位を有する重合体〔A〕1〜99重量%およ
び 一般式 ▲数式、化学式、表等があります▼ 〔式中、R^3、R^4はそれぞれ炭素数1〜5のアル
キル基あるいはフェニル基を示す。〕 で表わされる繰返し単位を有する重合体〔B〕99〜1
重量%を配合した組成物からなる光学機器用素材。(1) General formula ▲ Numerical formula, chemical formula, table, etc. ▼ [In the formula, R^1 and R^2 each represent an alkyl group or phenyl group having 1 to 5 carbon atoms, and X^1 and Each represents an alkyl group having 1 to 4 carbon atoms, an alkoxyl group having 1 to 4 carbon atoms, or a halogen atom. ] Polymer [A] having repeating units represented by 1 to 99% by weight and general formula ▲ Numerical formula, chemical formula, table, etc. ▼ [In the formula, R^3 and R^4 each have 1 to 5 carbon atoms Indicates an alkyl group or a phenyl group. ] Polymer [B] 99-1 having a repeating unit represented by
A material for optical equipment consisting of a composition containing % by weight.
9重量%である特許請求の範囲第1項記載の光学機器用
素材。(2) The blending ratio of polymer [A] in the composition is 80 to 9
The material for optical equipment according to claim 1, wherein the content is 9% by weight.
5g/dlの塩化メチレン溶液の還元粘度〔η_s_p
/c〕として0.3〜1.0dl/gである特許請求の
範囲第1項記載の光学機器用素材。(3) The viscosity of the polymer [A] at 25°C is 0.
Reduced viscosity of 5 g/dl methylene chloride solution [η_s_p
/c] is 0.3 to 1.0 dl/g.
5g/dlの塩化メチレン溶液の還元粘度〔η_s_p
/c〕として0.3〜1.0dl/gである特許請求の
範囲第1項記載の光学機器用素材。(4) The viscosity of the polymer [B] at 25°C is 0.
Reduced viscosity of 5 g/dl methylene chloride solution [η_s_p
/c] is 0.3 to 1.0 dl/g.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60148317A JPS6210160A (en) | 1985-07-08 | 1985-07-08 | Material for optical instrument |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60148317A JPS6210160A (en) | 1985-07-08 | 1985-07-08 | Material for optical instrument |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6210160A true JPS6210160A (en) | 1987-01-19 |
Family
ID=15450082
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60148317A Pending JPS6210160A (en) | 1985-07-08 | 1985-07-08 | Material for optical instrument |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6210160A (en) |
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JPS6462352A (en) * | 1987-09-01 | 1989-03-08 | Daicel Chem | Polymer composition having excellent compatibility |
JPS6462351A (en) * | 1987-09-01 | 1989-03-08 | Daicel Chem | Polymer composition having excellent compatibility |
JPS6469625A (en) * | 1987-09-10 | 1989-03-15 | Daicel Chem | Polycarbonate polymer having excellent surface hardness |
US5132154A (en) * | 1989-06-06 | 1992-07-21 | Bayer Aktiengesellschaft | Polycarbonate mixtures in optical applications |
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1985
- 1985-07-08 JP JP60148317A patent/JPS6210160A/en active Pending
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---|---|---|---|---|
JPS6443559A (en) * | 1987-08-12 | 1989-02-15 | Idemitsu Kosan Co | Polycarbonate resin composition |
JPS6462352A (en) * | 1987-09-01 | 1989-03-08 | Daicel Chem | Polymer composition having excellent compatibility |
JPS6462351A (en) * | 1987-09-01 | 1989-03-08 | Daicel Chem | Polymer composition having excellent compatibility |
JPS6469625A (en) * | 1987-09-10 | 1989-03-15 | Daicel Chem | Polycarbonate polymer having excellent surface hardness |
US5132154A (en) * | 1989-06-06 | 1992-07-21 | Bayer Aktiengesellschaft | Polycarbonate mixtures in optical applications |
US20130030112A1 (en) * | 2010-03-31 | 2013-01-31 | Tatsuya Hitomi | Polycarbonate resin composition, method for producing same and molded article of this resin composition |
US9771477B2 (en) | 2010-03-31 | 2017-09-26 | Mitsubishi Chemical Corporation | Polycarbonate resin composition, method for producing same and molded article of this resin composition |
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JP2017014530A (en) * | 2010-11-25 | 2017-01-19 | 三菱化学株式会社 | Polycarbonate resin composition and manufacturing method therefor |
JP2017020046A (en) * | 2010-11-25 | 2017-01-26 | 三菱化学株式会社 | Polycarbonate resin composition and method for producing the same |
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