JPS6390520A - Disk base using methacrylic resin composition as base - Google Patents
Disk base using methacrylic resin composition as baseInfo
- Publication number
- JPS6390520A JPS6390520A JP61237500A JP23750086A JPS6390520A JP S6390520 A JPS6390520 A JP S6390520A JP 61237500 A JP61237500 A JP 61237500A JP 23750086 A JP23750086 A JP 23750086A JP S6390520 A JPS6390520 A JP S6390520A
- Authority
- JP
- Japan
- Prior art keywords
- resin composition
- base
- methacrylic resin
- methyl methacrylate
- monomer
- 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.)
- Pending
Links
- 239000000113 methacrylic resin Substances 0.000 title claims description 10
- 239000000203 mixture Substances 0.000 title claims description 8
- 239000000178 monomer Substances 0.000 claims abstract description 19
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims abstract description 10
- IYMZEPRSPLASMS-UHFFFAOYSA-N 3-phenylpyrrole-2,5-dione Chemical class O=C1NC(=O)C(C=2C=CC=CC=2)=C1 IYMZEPRSPLASMS-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 5
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 5
- 230000000379 polymerizing effect Effects 0.000 claims abstract description 4
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims 1
- 230000003287 optical effect Effects 0.000 abstract description 9
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract description 4
- 239000011347 resin Substances 0.000 abstract description 4
- 229920005989 resin Polymers 0.000 abstract description 4
- 239000011342 resin composition Substances 0.000 abstract description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract description 2
- 238000000465 moulding Methods 0.000 abstract 2
- 229920001577 copolymer Polymers 0.000 description 5
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 3
- 125000005395 methacrylic acid group Chemical group 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- SFIRETRJZMGEOA-UHFFFAOYSA-N 1,3-dimethyl-4-phenylpyrrole-2,5-dione Chemical compound O=C1N(C)C(=O)C(C)=C1C1=CC=CC=C1 SFIRETRJZMGEOA-UHFFFAOYSA-N 0.000 description 1
- ZGKBRWPDSUWGHV-UHFFFAOYSA-N 1-ethyl-3-(2-methylphenyl)pyrrole-2,5-dione Chemical compound O=C1N(CC)C(=O)C=C1C1=CC=CC=C1C ZGKBRWPDSUWGHV-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、優れた透明性、耐熱性および成形加工性を有
する極めて実用的なメタクリル系樹脂を基盤とするディ
スク盤に関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a disc disk based on an extremely practical methacrylic resin having excellent transparency, heat resistance and moldability.
(従来の技術)
一般にポリメチルメタクリレート樹脂又はメチルメタク
リレートを主成分としたメタクリル系樹脂は、透明性、
表面光沢性、機械強度、成形性などの優れた特性から近
年光ファイノ々−1光学レンズおよび光ディスク等の光
学素子用材料としての需要が拡大しつつある。しかしそ
の熱変形温度に代表される耐熱性が劣るため高温での形
状安定性が要求される用途などにおいてはその使用に制
限を受けており、メタクリル系樹1盾の耐熱性を向上さ
せる研究が広く行なわれている。例えば、メチルメタク
リレート樹脂にマレイミド系単暫体を共重合させ、耐熱
性を向上させた共重合体からなる光デイスク基板(特開
昭61−95011号公報)が挙げられる。(Prior art) Generally, polymethyl methacrylate resin or methacrylic resin containing methyl methacrylate as a main component has transparency,
Due to its excellent properties such as surface gloss, mechanical strength, and moldability, the demand for it as a material for optical elements such as optical lenses and optical discs has been increasing in recent years. However, due to its poor heat resistance, as represented by its heat distortion temperature, its use is limited in applications that require shape stability at high temperatures, and research is underway to improve the heat resistance of methacrylic wood. It is widely practiced. For example, there is an optical disk substrate (Japanese Unexamined Patent Publication No. 61-95011) made of a copolymer obtained by copolymerizing a methyl methacrylate resin with a maleimide monomer to improve heat resistance.
(発明が解決しようとする問題点)
この特許により得られる共重合体(工、メタクリル系樹
脂が本米有する優れた特性を保持し、耐熱性を改善した
ものであるか、得られた基盤が黄色を呈した黄色透明で
ある為、特に光ビデオディスク、デジタルオーディオデ
ィスクおよび画像ファイル用ディスクなどの光デイスク
メモリシステムにおける光デイスク基盤等の透明性が要
求される用途においては、充分に満足できるものではな
く、着色のない、無色透明のディスク盤が望まれていた
。(Problem to be solved by the invention) Does the copolymer obtained by this patent retain the excellent properties of methacrylic resins and has improved heat resistance? Since it is transparent with a yellowish tint, it is particularly suitable for applications that require transparency, such as optical disk substrates in optical disk memory systems such as optical video disks, digital audio disks, and image file disks. Instead, a colorless and transparent disc with no coloring was desired.
(問題点を解決する為の手段)
本発明者は、この様な問題点に鑑み、機械的特性および
耐熱性に優れ、しかも無色透明のディスク盤を得るべく
、鋭意研究を重ねた結果、メチルメタアクリレートと特
定の置換フェニルマレイミドからなる共重合体より得ら
れるディスク盤が耐熱性に優れ、無色透明で複屈折率も
小さいことを見い出し本発明を完成するに至った。(Means for Solving the Problems) In view of the above problems, the inventors of the present invention have conducted intensive research to obtain a colorless and transparent disc with excellent mechanical properties and heat resistance. The present inventors have discovered that a disk obtained from a copolymer of methacrylate and a specific substituted phenylmaleimide has excellent heat resistance, is colorless and transparent, and has a low birefringence, and has completed the present invention.
すなわち本発明は、メチルメタクリレート55(式中、
R1、Rzはそれぞれ炭素数1〜3のアルキル基を表す
。)
で示される置換フェニルマレイミド単量体2−45重量
%およびこれらの単量体と共重合可能な他のビニル系単
量体O〜40重量%を重合してなるメタクリル系樹脂組
成物を基盤とするディスク盤である。That is, the present invention provides methyl methacrylate 55 (in the formula:
R1 and Rz each represent an alkyl group having 1 to 3 carbon atoms. ) Based on a methacrylic resin composition formed by polymerizing 2 to 45% by weight of a substituted phenylmaleimide monomer shown in It is a disc record.
本発明で使用するメチルメタクリレートとマレイミド系
単量体を共重合してなる共重合体自身(工特公昭43−
9753号公報により公知である。The copolymer itself obtained by copolymerizing methyl methacrylate and maleimide monomer used in the present invention
It is known from Japanese Patent No. 9753.
本発明の一般式(I)で示される置換フェニルマレイミ
ド単量体としては、具体的に【工例えば、N−2,6−
シメチルフエニルマレイミド、N−2,6−ジニチルフ
エニルマレイミド、N−2−エチル−6−メチルフェニ
ルマレイミドおよびN−2,6−ジプロピルフェニルマ
レイミド等が挙げられる。Specifically, the substituted phenylmaleimide monomer represented by the general formula (I) of the present invention may include [engineering, for example, N-2,6-
Examples include dimethylphenylmaleimide, N-2,6-dinitylphenylmaleimide, N-2-ethyl-6-methylphenylmaleimide, and N-2,6-dipropylphenylmaleimide.
また共重合可能なビニル系単量体としては、具体的には
例えば、アクリル酸、メタクリル酸、アクリル酸メチル
、アクリル酸エチル、メタクリル酸エチル、スチレン、
α−メチルスチレン、P−メチルスチレン及びアクリロ
ニトリル等が挙げられる。Specific examples of copolymerizable vinyl monomers include acrylic acid, methacrylic acid, methyl acrylate, ethyl acrylate, ethyl methacrylate, styrene,
Examples include α-methylstyrene, P-methylstyrene and acrylonitrile.
本発明で使用する共重合体は、メチルメタクリレート5
5〜98重量係、好ましくは65〜90重量%含有する
ことが必要である。メチルメタクリレートが55重量%
未満では、透明性、複屈折率及び機械的強度が低下し好
ましくない。一般式(υで示される置換フェニルマレイ
ミド単量体は、2〜45重量%、好ましく【工10〜3
03i量チ含有することが必要である。置換フェニルマ
レイミド単量体が、2重量子未満では耐熱性が低下し、
45:!Et%を越えて含有した場合、機械的強度及び
高温成形性が低下する為、実用上問題が有る。The copolymer used in the present invention is methyl methacrylate 5
It is necessary to contain 5 to 98% by weight, preferably 65 to 90% by weight. 55% by weight of methyl methacrylate
If it is less than this, transparency, birefringence and mechanical strength will deteriorate, which is not preferable. The substituted phenylmaleimide monomer represented by the general formula (υ) is preferably 2 to 45% by weight, preferably
It is necessary to contain an amount of 03i. If the substituted phenylmaleimide monomer is less than 2 quantum molecules, heat resistance decreases,
45:! If the content exceeds Et%, mechanical strength and high-temperature formability will decrease, causing a practical problem.
また、Cれらの単量体と共重合可能な他のビニル系単量
体は0〜40重量%、好ましく(工0〜20重量%含有
させる、このビニル系単量体が40重量%を越えると、
透明性及び着色の問題が生じ好ましくない。また本発明
のメタクル系樹脂組成物は、紫外線吸収剤などの光安定
剤、酸化防止剤などの熱安定剤等を含有させることがで
きる。Further, other vinyl monomers copolymerizable with these monomers are contained in an amount of 0 to 40% by weight, preferably 0 to 20% by weight. When you cross it,
Problems with transparency and coloration occur, which is undesirable. The methacrylic resin composition of the present invention can also contain light stabilizers such as ultraviolet absorbers, heat stabilizers such as antioxidants, and the like.
禾発明のメタクリル系樹脂組成物の重合方法は通常公知
の方法に従い、重合することができる。The methacrylic resin composition of the present invention can be polymerized according to a commonly known method.
たとえば、ラジカル重合開始剤の存在下、前記重合成分
を50〜95℃の温度範囲で懸濁重合、塊状重合、乳化
重合および溶液重合等の各種の方法を用いることができ
る。この際、開始剤の他に、連鎖移動剤と通常の懸濁剤
、助剤等を用いることもできる。さらにこの様にして得
られたメタクリル系樹脂組成物を、目的に応じた形状お
よび大きさを有するディスク盤に射出成形、圧縮成形な
どの方法により成形することができる。普だ、本発明の
メタクリル系樹脂組成嘗は、光学レンズ、自動車部品等
として利用することもできる。For example, various methods such as suspension polymerization, bulk polymerization, emulsion polymerization, and solution polymerization of the polymerization components can be used in the presence of a radical polymerization initiator at a temperature of 50 to 95°C. At this time, in addition to the initiator, a chain transfer agent, a usual suspending agent, an auxiliary agent, etc. can also be used. Furthermore, the methacrylic resin composition thus obtained can be molded into a disk having a shape and size depending on the purpose by injection molding, compression molding, or the like. Generally, the methacrylic resin composition of the present invention can also be used as optical lenses, automobile parts, etc.
(効果)
本返明は、メチルメタクリレートと共重合させる単量体
として2,6−ジアルキル置換フェニルマレイミドを選
択することにより、従来メタクリル系樹脂の有する機械
的強度、成形性を保持し、耐熱性を向上させるだけでな
く無色透明のディスク盤を得ることを可能にしたもので
ある。(Effects) By selecting 2,6-dialkyl-substituted phenylmaleimide as a monomer to be copolymerized with methyl methacrylate, the present invention maintains the mechanical strength and moldability of conventional methacrylic resins, and has excellent heat resistance. This not only improves the quality of the disc, but also makes it possible to obtain a colorless and transparent disc.
(実施例) 以下、実施例により本発明をさらに詳剣に説明する。(Example) Hereinafter, the present invention will be explained in more detail with reference to Examples.
実施例1
メチルメタクリレート90部、N−2,6−ジニチルフ
エニルマレイミド10部およびアゾビスイソブチロニト
リル0.5部を容器の中で混合加熱した。生成したシロ
ップを二枚のガラス板(距離0.32m)セルに満し、
75℃で6時間保った後、95℃で2時間保つことによ
り樹脂組成物を得た。Example 1 90 parts of methyl methacrylate, 10 parts of N-2,6-dinitylphenylmaleimide, and 0.5 part of azobisisobutyronitrile were mixed and heated in a container. Fill a cell with two glass plates (distance 0.32 m) with the produced syrup,
A resin composition was obtained by keeping at 75°C for 6 hours and then at 95°C for 2 hours.
実施例2〜6、比較例1〜4
実施例1のマレイミドの種類およびそれぞれの単量体の
割合を表−1に示すような樹脂組成物を製造した。Examples 2 to 6, Comparative Examples 1 to 4 Resin compositions having the type of maleimide and the proportion of each monomer of Example 1 shown in Table 1 were manufactured.
表 −1
比較2 90 ”江;けレイミド −0(
成形品による物性)
実施例1〜6及び比較例1〜4で得られたメタクリル系
樹脂組成物を射出成形し各物性を測定した。尚、耐熱変
形性()[)T)はASTM−D648に従い、光透過
率はJIS−に−6714に従い複屈折率は、射出成形
(シリンダー温度260’Q金型温度60℃)によって
得た厚さ1.2Bの板を用いて、精密歪計を用いて測定
した。Table -1 Comparison 2 90 ``E;kereimido -0(
Physical properties of molded articles) The methacrylic resin compositions obtained in Examples 1 to 6 and Comparative Examples 1 to 4 were injection molded and their physical properties were measured. The heat deformation resistance ()[)T) is in accordance with ASTM-D648, the light transmittance is in accordance with JIS-6714, and the birefringence is in accordance with the thickness obtained by injection molding (cylinder temperature 260'Q mold temperature 60°C). Measurements were made using a precision strain meter using a 1.2B plate.
結果を表−2に示す。The results are shown in Table-2.
表 −2
盃 HDT (℃) 光透過率(チフ 複屈折(
n、) 着色性実施例1 115 90
15 無色透明覧
6 125 δδ 1δ
比較1 95 92 8Table-2 Cup HDT (°C) Light transmittance (typ. Birefringence (
n,) Colorability Example 1 115 90
15 Colorless transparent view 6 125 δδ 1δ Comparison 1 95 92 8
Claims (1)
キル基を表す。) で示される置換フェニルマレイミド単量体2−45重量
%およびこれらの単量体と共重合可能な他のビニル系単
量体0〜40重量%を重合してなるメタクリル系樹脂組
成物を基盤とするディスク盤。[Claims] Methyl methacrylate 55-98% by weight, represented by the general formula ▲ Numerical formula, chemical formula, table, etc. ▼ (In the formula, R_1 and R_2 each represent an alkyl group having 1 to 3 carbon atoms.) A disc disk based on a methacrylic resin composition formed by polymerizing 2-45% by weight of a substituted phenylmaleimide monomer and 0-40% by weight of another vinyl monomer copolymerizable with these monomers. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61237500A JPS6390520A (en) | 1986-10-06 | 1986-10-06 | Disk base using methacrylic resin composition as base |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61237500A JPS6390520A (en) | 1986-10-06 | 1986-10-06 | Disk base using methacrylic resin composition as base |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6390520A true JPS6390520A (en) | 1988-04-21 |
Family
ID=17016237
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61237500A Pending JPS6390520A (en) | 1986-10-06 | 1986-10-06 | Disk base using methacrylic resin composition as base |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6390520A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4235643A1 (en) * | 1992-09-25 | 1994-04-28 | Chemie Linz Deutschland | Polymers and polymer dispersions and their use in hydraulic binders |
-
1986
- 1986-10-06 JP JP61237500A patent/JPS6390520A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4235643A1 (en) * | 1992-09-25 | 1994-04-28 | Chemie Linz Deutschland | Polymers and polymer dispersions and their use in hydraulic binders |
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