JPH0232681B2 - - Google Patents
Info
- Publication number
- JPH0232681B2 JPH0232681B2 JP54154895A JP15489579A JPH0232681B2 JP H0232681 B2 JPH0232681 B2 JP H0232681B2 JP 54154895 A JP54154895 A JP 54154895A JP 15489579 A JP15489579 A JP 15489579A JP H0232681 B2 JPH0232681 B2 JP H0232681B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- disc record
- disc
- ultraviolet curable
- weight
- 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
Links
- 229920005989 resin Polymers 0.000 claims description 33
- 239000011347 resin Substances 0.000 claims description 33
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 3
- 229920001577 copolymer Polymers 0.000 claims description 3
- 239000003999 initiator Substances 0.000 claims description 3
- 239000001294 propane Substances 0.000 claims description 3
- 239000012790 adhesive layer Substances 0.000 claims description 2
- 239000012461 cellulose resin Substances 0.000 claims description 2
- 229920005668 polycarbonate resin Polymers 0.000 claims description 2
- 239000004431 polycarbonate resin Substances 0.000 claims description 2
- 229920000193 polymethacrylate Polymers 0.000 claims description 2
- 229920005990 polystyrene resin Polymers 0.000 claims description 2
- 239000011342 resin composition Substances 0.000 claims 1
- 239000007788 liquid Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 5
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- 238000001723 curing Methods 0.000 description 3
- 229910003460 diamond Inorganic materials 0.000 description 3
- 239000010432 diamond Substances 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000008014 freezing Effects 0.000 description 2
- 238000007710 freezing Methods 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- YDKNBNOOCSNPNS-UHFFFAOYSA-N methyl 1,3-benzoxazole-2-carboxylate Chemical group C1=CC=C2OC(C(=O)OC)=NC2=C1 YDKNBNOOCSNPNS-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Landscapes
- Optical Record Carriers And Manufacture Thereof (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
- Polymerisation Methods In General (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Description
本発明はオーデイオデイスク、ビデオデイスク
などのデイスクレコードに関するもので、特に原
盤からこれらのデイスクレコードを製造する際に
原盤の表面に刻み込まれた信号に忠実な表面構造
を有し、しかもレコード針などの機械的な方法に
よつて信号を再生する場合には、そのデイスクレ
コードに溝に刻み込まれた信号がレコード針によ
つて摩耗されたりすることのないデイスクレコー
ドを提供しようとするものである。
レコード工業の分野では、オーデイオデイスク
を得るために、たとえば金属表面の溝に信号が刻
み込まれたオリジナル原盤(スタンパー)を用い
て、主に塩化ビニルと酢酸ビニルの共重合体を圧
縮成形して、デイスクレコードを製作している。
しかし、高密度の信号を有するデイスクたとえば
ビデオデイスクにおいては、その記録信号の刻み
込まれている構造が非常に微細であるため、成形
の不精確さによつて良好な再生信号が得られない
という問題がある。
このため、スタンパーに刻み込まれている信号
に忠実な信号を有するデイスクレコードを製造す
るための技術が要求されている。また、ダイアモ
ンド針などで信号を再生する場合には、デイスク
に刻み込まれている信号が摩耗したり変形したり
することのない耐摩耗性のよいデイスクレコード
が強く望まれている。また一方、生産面からはデ
イスクレコードの製造後、スタンパーからの剥離
が容易であること、すなわちスタンパーとの密着
性を有していないことが必要である。
本発明はこのような要望を満足させるものであ
り、デイスクレコードを製造する方法として、た
とえば信号の刻み込まれたスタンパー表面の一部
分または全体に紫外線の照射によつて硬化可能な
液状樹脂を被覆し、ついでその上より透明プレー
トからなる支持体を圧着して前記液状樹脂を均一
な厚みとなるようにする。ついで支持体を通して
紫外線を照射して液状樹脂を硬化させ、そののち
支持体を、それに付着した硬化樹脂とともにスタ
ンパーから剥離することによつてデイスクレコー
ドが得られる。支持体の他の面についても上述と
同じ操作を同時に、あるいは個別に行なえば、支
持体の両面に信号の刻み込まれた樹脂皮膜を有す
るデイスクレコードが得られる。
紫外線の照射によつて硬化可能な液状樹脂とし
て、紫外線硬化型樹脂成分としては、下記構造式
()で表わされる2,2−ビス(4−アクリロ
イルオキシポリエチレンオキシフエニル)プロパ
ンのみを含む紫外線硬化型樹脂と、2〜4重量
%、好ましくは3重量%の光重合開始剤を含んで
いるものである。
(ただし、m,nは整数でmとnの合計が3〜
4)。
これを用いることによつてスタンパーとの剥離
性およびスタンパー表面に刻み込まれた信号転写
の忠実性に優れ、またダイアモンド針による耐摩
耗性もきわめて良好なデイスクレコードができ
た。この理由としては、本願発明の紫外線硬化型
樹脂の収縮率が5.8%と低く、例えばビツカース
硬度も10程度と低いことによるためである。な
お、光重合開始剤の添加量が2重量%より少なく
なると、光硬化させるのに要する時間が増大し、
デイスクレコードの生産性が低下する。一方、添
加量があまり多すぎると硬化皮膜特性、特に機械
的特性が低下する。
以下、本発明の実施例について、図面を用いて
説明する。
第1図はデイスクレコードの平面図、第2図は
そのX−X′線における断面図を拡大したもので
ある。デイスクレコードは、少なくとも塩化ビニ
ルと酢酸ビニルの共重合体、ポリメタクリル酸エ
ステル樹脂、ポリスチレン樹脂、ポリカーボネー
ト樹脂、繊維素系樹脂または表面に接着層を設け
た上記樹脂からなる紫外線透過性のプレート支持
体1と、紫外線硬化型樹脂皮膜2からなり、その
皮膜2の表面には信号が刻み込まれた溝3が施さ
れている。紫外線硬化型樹脂皮膜は97重量%の
2,2−ビス(4−アクリロイルオキシジエチレ
ンオキシフエニル)プロパンからなる紫外線硬化
型樹脂と3重量%のベンゾインイソプロピルエー
テルからなるものである。
この本実施例の紫外線硬化型樹脂(UV樹脂)
の平均分子量は約510で、低分子量ながら、その
粘度係数は約2000cpであり、基板に押し付けて
も気泡が入りにくく、品質の安定したデイスクレ
コードが得られる。
ここで分子量と粘度との関係について説明す
る。
同一種類のポリマー(例えば分子量の違うアク
リル樹脂など)においては、分子量と粘度(ある
溶剤に一定量を溶かした溶液の粘度)との間には
関連性が見られる。
即ち、溶液粘度を測定することによつてポリマ
ーの分子量(この場合は、粘度平均分子量と呼ば
れている)を求める手法が確立されている。
しかし、普通の低分子系の分子あるいは異なる
種類の分子間では規制的な関連性が認められてい
ないのが現実である。
例えば、トリメチロールプロパントリアクリレ
ート(分子量296)が25℃で約70cpに対し、ペン
タエリスリトールトリアクリレート(分子量298)
は、25℃で約770cpを示す。
このように、特に低分子系の異なる分子間の粘
度については、分子間の相互作用(例えば分子間
の水素結合、極性基間のクーロンカなど)が強け
れば強いほど、流動性がなくなり、粘度が高くな
る。また、分子の形状が長くなれば、同じ分子量
でも、それだけ分子間のからまりができ、粘度の
増大を伴う。さらに凝固点にも関連し、凝固点近
くでは、一部結晶化のため、分子間の相互作用が
強くなり、粘度が増大するものと思われる。
以上のように、低分子系の分子からなる物質の
粘度は、勿論、その分子個体の分子量にも若干影
響を受けるが、それ以外にも、その分子の集合体
としての特性、例えば分子間の相互作用、分子の
形状による分子同志のからまり等々によつて大き
く左右される。
また、本実施例のUV樹脂は皮膚一次刺激性指
数が0.8であり、他の樹脂(例えば、ブタンジオ
ールジアクリレート8.0、トリメチロールプロパ
ントリアクリレートの4.6)の指数と比較しても、
その値は本実施例の樹脂の方が小さく、安全衛生
上、取扱いにおいて優れている。
さらに、この皮膜2は、スタンパーとの剥離性
が良好で、また特に信号を刻み込んだ溝3のダイ
アモンド針に対する耐摩耗性もきわめて優れてい
るものである。
下表は、本実施例の紫外線硬化型樹脂の硬化皮
膜およびその一部を低分子系のUV樹脂で稀釈し
た材料の硬化皮膜、例えば比較例1として、ネオ
ペンチルグリコールジアクリレートで20wt%を
置換した材料の硬化皮膜、および比較例2とし
て、トリメチロールプロパントリアクリレート
The present invention relates to disc records such as audio discs and video discs, and in particular has a surface structure that is faithful to the signal engraved on the surface of the master disc when these disc records are manufactured from the master disc, and has a surface structure that is faithful to the signal engraved on the surface of the master disc when manufacturing these disc records from the master disc. When a signal is reproduced by a mechanical method, it is an object of the present invention to provide a disc record in which the signals engraved in the grooves of the disc record are not worn away by the record stylus. In the field of the record industry, to obtain audio discs, for example, original master discs (stampers) with signals engraved in grooves on the metal surface are used, and a copolymer of vinyl chloride and vinyl acetate is compression molded. Producing disc records.
However, in discs with high-density signals, such as video discs, the structure in which the recorded signals are engraved is very fine, so there is a problem that good reproduction signals cannot be obtained due to the inaccuracy of molding. There is. Therefore, there is a need for a technique for manufacturing a disc record having a signal that is faithful to the signal engraved on the stamper. Furthermore, when reproducing signals using a diamond stylus or the like, there is a strong desire for a disc record with good wear resistance so that the signals engraved on the disc will not be worn out or deformed. On the other hand, from a production standpoint, it is necessary that the disc record be easily peeled off from the stamper after manufacturing, that is, it must not have adhesion to the stamper. The present invention satisfies these demands and is a method for manufacturing a disc record, for example, by coating a part or the entire surface of a stamper on which a signal is engraved with a liquid resin that can be cured by irradiation with ultraviolet rays. Then, a support made of a transparent plate is pressed onto the support so that the liquid resin has a uniform thickness. Next, the liquid resin is cured by irradiating ultraviolet rays through the support, and then the support is peeled off from the stamper together with the cured resin adhering to it, thereby obtaining a disc record. If the same operations as described above are carried out simultaneously or separately on the other surfaces of the support, a disc record having a resin film with signals engraved on both sides of the support can be obtained. As a liquid resin that can be cured by irradiation with ultraviolet rays, an ultraviolet curable resin containing only 2,2-bis(4-acryloyloxypolyethyleneoxyphenyl)propane represented by the following structural formula () is used as an ultraviolet curable resin component. It contains a mold resin and 2 to 4% by weight, preferably 3% by weight of a photopolymerization initiator. (However, m and n are integers, and the sum of m and n is 3~
4). By using this, a disc record was produced which had excellent removability from the stamper and fidelity of signal transfer engraved on the stamper surface, and also had extremely good abrasion resistance due to diamond needles. The reason for this is that the shrinkage rate of the ultraviolet curable resin of the present invention is as low as 5.8%, and the Vickers hardness is also as low as about 10, for example. Note that when the amount of photopolymerization initiator added is less than 2% by weight, the time required for photocuring increases,
Disk record productivity decreases. On the other hand, if the amount added is too large, the properties of the cured film, especially the mechanical properties, will deteriorate. Embodiments of the present invention will be described below with reference to the drawings. FIG. 1 is a plan view of the disc record, and FIG. 2 is an enlarged cross-sectional view taken along line X-X'. The disc record is an ultraviolet-transparent plate support made of at least a copolymer of vinyl chloride and vinyl acetate, polymethacrylate resin, polystyrene resin, polycarbonate resin, cellulose resin, or any of the above resins with an adhesive layer provided on the surface. 1 and an ultraviolet curing resin film 2, the surface of the film 2 is provided with grooves 3 in which signals are carved. The ultraviolet curable resin film consists of an ultraviolet curable resin consisting of 97% by weight of 2,2-bis(4-acryloyloxydiethyleneoxyphenyl)propane and 3% by weight of benzoin isopropyl ether. Ultraviolet curing resin (UV resin) of this example
The average molecular weight of this material is approximately 510, and although it has a low molecular weight, its viscosity coefficient is approximately 2000 cp, so even when pressed against a substrate, air bubbles are unlikely to form, making it possible to obtain disc records of stable quality. Here, the relationship between molecular weight and viscosity will be explained. For polymers of the same type (for example, acrylic resins with different molecular weights), there is a relationship between molecular weight and viscosity (viscosity of a solution of a certain amount dissolved in a certain solvent). That is, a method has been established for determining the molecular weight of a polymer (in this case, called viscosity average molecular weight) by measuring the solution viscosity. However, the reality is that no regulatory relationships have been recognized between ordinary low-molecular-weight molecules or between different types of molecules. For example, trimethylolpropane triacrylate (molecular weight 296) is approximately 70 cp at 25°C, whereas pentaerythritol triacrylate (molecular weight 298)
shows approximately 770 cp at 25°C. In this way, with regard to the viscosity between different molecules, especially in low-molecular systems, the stronger the interactions between molecules (for example, hydrogen bonds between molecules, Coulombic forces between polar groups, etc.), the less fluidity becomes, and the viscosity decreases. It gets expensive. Further, as the shape of the molecules becomes longer, even if the molecular weight is the same, entanglement between molecules occurs, which is accompanied by an increase in viscosity. Furthermore, it is related to the freezing point, and it is thought that near the freezing point, due to some crystallization, the interaction between molecules becomes stronger and the viscosity increases. As mentioned above, the viscosity of a substance made of low-molecular-weight molecules is, of course, slightly affected by the molecular weight of each individual molecule, but it is also affected by the characteristics of the aggregate of the molecules, such as the It is greatly influenced by interactions, entanglement of molecules due to their shape, etc. In addition, the UV resin of this example has a primary skin irritation index of 0.8, which is even compared to the index of other resins (e.g., butanediol diacrylate: 8.0, trimethylolpropane triacrylate: 4.6).
The resin of this example has a smaller value and is superior in terms of safety and hygiene and handling. Furthermore, this coating 2 has good releasability from the stamper, and is particularly excellent in abrasion resistance against diamond needles in the grooves 3 in which the signals are engraved. The table below shows the cured film of the UV-curable resin of this example and the cured film of a material partially diluted with low-molecular-weight UV resin, for example, as Comparative Example 1, 20 wt% was replaced with neopentyl glycol diacrylate. The cured film of the cured material, and as Comparative Example 2, trimethylolpropane triacrylate
【表】
尚、針による摩耗に対しては、ある程度の柔ら
かさが必要で、UV樹脂では、多官能の低分子
UV樹脂で置換て硬くするともろくなり、針によ
るけずりくずが発生しやすくなる。
また、硬度としては11以下が望ましいといわれ
ている。
なお、皮膜2の性質を変性させるために、紫外
線により硬化する液状樹脂には種々の添加剤を加
えることができる。たとえば、着色のための染
料、液状樹脂の脱泡性、スタンパーとの濡れをよ
くするための脱泡剤、湿潤剤などの界面活性剤、
あるいは紫外線照射の際にランプから発生する熱
を有効に利用するための有機過酸化物などの熱硬
化触媒などがある。[Table] Note that a certain degree of softness is required to withstand abrasion caused by needles, and UV resins require polyfunctional low-molecular
If it is hardened by replacing it with UV resin, it will become brittle and more likely to be scratched by needles. Further, it is said that a hardness of 11 or less is desirable. In addition, in order to modify the properties of the film 2, various additives can be added to the liquid resin that is cured by ultraviolet rays. For example, dyes for coloring, defoaming properties of liquid resin, defoaming agents to improve wetting with stampers, surfactants such as wetting agents,
Alternatively, there are thermosetting catalysts such as organic peroxides that effectively utilize the heat generated from the lamp during ultraviolet irradiation.
第1図は本発明にかかるデイスクレコードの一
実施例を示す部分的平面図であり、第2図はその
X−X′線に沿つた断面図である。
1……プレート支持体、2……紫外線硬化型樹
脂皮膜、3……溝。
FIG. 1 is a partial plan view showing an embodiment of a disc record according to the present invention, and FIG. 2 is a sectional view taken along the line X-X'. 1... Plate support, 2... Ultraviolet curing resin film, 3... Groove.
Claims (1)
は両面に、情報を表わす凹凸を表面上に有する紫
外線硬化型樹脂皮膜を施してなるデイスクレコー
ドにおいて、前記樹脂皮膜が、紫外線硬化型樹脂
成分としては、下記構造式()で表わされる
2,2−ビス(4−アクリロイルオキシポリエチ
レンオキシフエニル)プロパンのみを含むととも
に、2〜4重量%の光重合開始剤を含んでいる樹
脂組成物を硬化させて得られたものであることを
特徴とするデイスクレコード。 (ただし、m,nは整数でmとnの合計が3〜
4) 2 透明プレートが少なくとも塩化ビニルと酢酸
ビニルの共重合体、ポリメタクリル酸エステル樹
脂、ポリスチレン樹脂、ポリカーボネート樹脂、
繊維素系樹脂または表面に接着層を設けた上記樹
脂で構成されていることを特徴とする特許請求の
範囲第1項記載のデイスクレコード。[Scope of Claims] 1. A disc record in which a transparent plate is used as a support and an ultraviolet curable resin film having unevenness representing information on the surface is applied to one or both sides, wherein the resin film is an ultraviolet curable resin film. As a resin component, a resin composition containing only 2,2-bis(4-acryloyloxypolyethyleneoxyphenyl)propane represented by the following structural formula () and 2 to 4% by weight of a photopolymerization initiator A disc record characterized by being obtained by curing a material. (However, m and n are integers, and the sum of m and n is 3~
4) 2 The transparent plate is made of at least a copolymer of vinyl chloride and vinyl acetate, a polymethacrylate resin, a polystyrene resin, a polycarbonate resin,
The disc record according to claim 1, characterized in that it is made of a cellulose resin or the above-mentioned resin with an adhesive layer provided on its surface.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15489579A JPS5677905A (en) | 1979-11-28 | 1979-11-28 | Disk record |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15489579A JPS5677905A (en) | 1979-11-28 | 1979-11-28 | Disk record |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5677905A JPS5677905A (en) | 1981-06-26 |
JPH0232681B2 true JPH0232681B2 (en) | 1990-07-23 |
Family
ID=15594297
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15489579A Granted JPS5677905A (en) | 1979-11-28 | 1979-11-28 | Disk record |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5677905A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5687203A (en) * | 1979-12-18 | 1981-07-15 | Toppan Printing Co Ltd | Manufacture of disk |
JPS56127946A (en) * | 1980-03-12 | 1981-10-07 | Matsushita Electric Ind Co Ltd | Disk-type recording medium |
JPS5838125A (en) * | 1981-09-01 | 1983-03-05 | Toppan Printing Co Ltd | Manufacture of information record carrier |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5271585A (en) * | 1975-10-20 | 1977-06-15 | Matsui Kagaku Kougiyoushiyo Kk | Photoocuring composition |
JPS5375291A (en) * | 1976-12-17 | 1978-07-04 | Toagosei Chem Ind Co Ltd | Casting composition |
JPS5386756A (en) * | 1976-10-15 | 1978-07-31 | Philips Nv | Plastic information carrier duplicating process and plastic record carrier and molding resin |
JPS53104638A (en) * | 1977-02-23 | 1978-09-12 | Mitsubishi Rayon Co Ltd | Coating composition and preparation of abrasion resistant synthetic resin molded artticle using the same |
JPS53116105A (en) * | 1977-03-14 | 1978-10-11 | Philips Nv | Method and device for making plastic record |
JPS55157107A (en) * | 1979-05-22 | 1980-12-06 | Matsushita Electric Ind Co Ltd | Disc record |
JPS55160338A (en) * | 1979-05-25 | 1980-12-13 | Philips Nv | Optically readable information disk* method and apparatus for fabricating same |
-
1979
- 1979-11-28 JP JP15489579A patent/JPS5677905A/en active Granted
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5271585A (en) * | 1975-10-20 | 1977-06-15 | Matsui Kagaku Kougiyoushiyo Kk | Photoocuring composition |
JPS5386756A (en) * | 1976-10-15 | 1978-07-31 | Philips Nv | Plastic information carrier duplicating process and plastic record carrier and molding resin |
JPS5375291A (en) * | 1976-12-17 | 1978-07-04 | Toagosei Chem Ind Co Ltd | Casting composition |
JPS53104638A (en) * | 1977-02-23 | 1978-09-12 | Mitsubishi Rayon Co Ltd | Coating composition and preparation of abrasion resistant synthetic resin molded artticle using the same |
JPS53116105A (en) * | 1977-03-14 | 1978-10-11 | Philips Nv | Method and device for making plastic record |
JPS55157107A (en) * | 1979-05-22 | 1980-12-06 | Matsushita Electric Ind Co Ltd | Disc record |
JPS55160338A (en) * | 1979-05-25 | 1980-12-13 | Philips Nv | Optically readable information disk* method and apparatus for fabricating same |
Also Published As
Publication number | Publication date |
---|---|
JPS5677905A (en) | 1981-06-26 |
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