JPS5887183A - Optical recording material - Google Patents

Optical recording material

Info

Publication number
JPS5887183A
JPS5887183A JP56184496A JP18449681A JPS5887183A JP S5887183 A JPS5887183 A JP S5887183A JP 56184496 A JP56184496 A JP 56184496A JP 18449681 A JP18449681 A JP 18449681A JP S5887183 A JPS5887183 A JP S5887183A
Authority
JP
Japan
Prior art keywords
wavelength
recording material
optical recording
shows
spectral characteristics
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.)
Granted
Application number
JP56184496A
Other languages
Japanese (ja)
Other versions
JPS6356920B2 (en
Inventor
Takushi Hirono
廣野 卓志
Tomoaki Yamada
山田 智秋
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 Telegraph and Telephone Corp
Original Assignee
Nippon Telegraph and Telephone 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 Nippon Telegraph and Telephone Corp filed Critical Nippon Telegraph and Telephone Corp
Priority to JP56184496A priority Critical patent/JPS5887183A/en
Publication of JPS5887183A publication Critical patent/JPS5887183A/en
Publication of JPS6356920B2 publication Critical patent/JPS6356920B2/ja
Granted legal-status Critical Current

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  • Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
  • Silicates, Zeolites, And Molecular Sieves (AREA)
  • Optical Record Carriers And Manufacture Thereof (AREA)

Abstract

PURPOSE:To provide an optical recording material which can be produced by a simple production process, does not require any fixing treatments, and makes rewriting possible, consisting of an Ag2O/SiO2 compd. CONSTITUTION:An optical recording material consists of an Ag2O/SiO2 compd. Examples of said Ag2O/SiO2 compds. are Ag4SiO4, Ag2SiO3 and Ag2SiO5. This compd. turns black by light irradiation and is discolored by heating. The resulting optical recording material has the following advantages. (1) Fixing is not required. (2) photosenitive sensitivity is high. (3) It is possible to choose photosensitive wave range by changing the composition ratio of Ag2O to SiO2. (4) The material is thermally stable because it is a crystalline material. (5) Any elaborate production stages are not required.

Description

【発明の詳細な説明】 する。[Detailed description of the invention] do.

銀A7 と二酸化ケイ素Si○2 を含む感光材料とし
ては、フォトクロミックガラスが知られている。これは
’t Si02及びB203 を主成分としたガラスマ
トリックス中に、銀と・・ロケンを導入し、600℃〜
700℃ の温度で数十分〜数時間熱処理し、感光体と
なるノ・ロゲン化銀微粒子を析出させたものである。フ
ォトクロミックガラスは、紫外光及び可視光の照射(で
より黒rヒし、また加熱することにより速やかに退色す
るため、書換え可能な記録材料として使用しうるもので
ある。しかし、銅Cu等の添加物の導入及びガラス製造
中に飛散しやすいA2やハロゲンの量の最適化を図るた
めに、製造工程が複雑であったり、捷だ感光波長の長波
や難しく、更に室温においても退色して記録が失われる
等の欠点があった。
Photochromic glass is known as a photosensitive material containing silver A7 and silicon dioxide Si○2. This is done by introducing silver and Roken into a glass matrix mainly composed of Si02 and B203, and heating it at 600℃~
It is heat-treated at a temperature of 700° C. for several tens of minutes to several hours to precipitate fine silver halogenide particles that will become a photoreceptor. Photochromic glass can be used as a rewritable recording material because it becomes darker when irradiated with ultraviolet light and visible light, and quickly fades when heated. However, it can be used as a rewritable recording material. In order to optimize the amount of A2 and halogens that are easily scattered during the introduction of materials and glass manufacturing, we have to avoid cases where the manufacturing process is complex, the wavelength of the photosensitive material is long and difficult, and the color fades even at room temperature, making recording difficult. There were drawbacks such as loss of information.

本発明の目的は、製造方法が簡便で、定着処理が不要で
あシ、且つ書換え可能な光学記録材料を提供するにある
An object of the present invention is to provide an optical recording material that is easy to manufacture, does not require a fixing process, and is rewritable.

すなわち本発明を概説すh,ば、本発明は、A y2 
0  S 1. 02系の化合物で構成することを特徴
とする光学記録材料に関する。
That is, to summarize the present invention, h, the present invention is A y2
0 S 1. The present invention relates to an optical recording material characterized by being composed of a 02-based compound.

Ayz 0 − Si02系の化合物としては、従来、
Ay4Si04、Ag3 Sj.2 07、 Ayz 
S103及びAyz SjzOsが知られており、それ
らの合成法も公知である〔E、10 ( E. Thj
.]−o )、F.ウオトク( F. Wodtcke
)〃ツアイト/ユリフト フユール アンオル力ニッシ
エ ラント アルゲマイネ  ヘミー〃(Z、  an
org、  al]−g、  Chem、 )  24
7.  p295(j978)及びV、 M、  ヤン
セン(V、 M、 Jansen ) 〃アクタフリス
タロブラフイカ“(Acta Cryst、 ) B 
33゜p3584 ’(1977)参照〕。
As Ayz 0 - Si02 type compounds, conventionally,
Ay4Si04, Ag3Sj. 2 07, Ayz
S103 and Ayz SjzOs are known, and their synthesis methods are also known [E, 10 (E. Thj
.. ]-o), F. F. Wodtcke
)〃Zait/Urift Fuyur Anorikinissier Land Allgemeine Hemy〃(Z, an
org, al]-g, Chem, ) 24
7. p295 (j978) and V, M, Jansen (Acta Cryst, ) B
33° p. 3584' (1977)].

これらの化合物の光学的性質は未知であったが、感光性
を調べた結果、光照射により黒化し、加熱により退色す
ることを見出し7た。
Although the optical properties of these compounds were unknown, as a result of examining their photosensitivity, they found that they turned black when exposed to light and faded when heated7.

本発明のAg2O−Si 02 系2成分酸化物光学記
録材利け、これら化合物自体が感光性を有し、加熱する
ことにより容易に記録を消去することができるので、記
録・消去を繰返すことができる点に特徴がある。そのた
め、 (1)定着が不要である。
Using the Ag2O-Si02 based binary oxide optical recording material of the present invention, these compounds themselves have photosensitivity and recording can be easily erased by heating, so recording and erasing can be repeated. It is characterized by what it can do. Therefore, (1) Fixation is not necessary.

(2)  感光感度が高い。(2) High photosensitivity.

(3)  へy20− Sl 02系の成分比を変える
ことにより、感光波長域を選択することが可能である。
(3) By changing the component ratio of the y20-Sl02 system, it is possible to select the sensitive wavelength range.

(4)結晶性(オ料であるため、熱的に安定である。(4) Crystallinity (because it is an oxide, it is thermally stable.

(5)  製造工程に特殊な]二夫を要しない。(5) No special second husband is required in the manufacturing process.

という利点がある。There is an advantage.

以下、実施例により本発明の詳細な説明するが、本発明
はこれらに限宇されるものではない。
Hereinafter, the present invention will be explained in detail with reference to Examples, but the present invention is not limited thereto.

なお添付図面について概説すると、第1図は、Ay4S
j、04の反射分光特性を、波1%: (nm) (横
軸)と反射率(係)(縦軸)との関係で表すグラフであ
る。第2図ば、A24S104の分光感度を、照射波長
(nm) (横軸)と光照射足よる波長7001111
1における反射率の低下(係)(縦軸)との関係で表す
グラフである。第3図(dム A45j03の反射分光
特性を、前記関係で表すグラフである。第4図は、A 
y281.03の分光感度を、前記間・係で表すグラフ
である。第5図(は、380℃で熱処理したQ2Sj 
O3の反射分光特性を、前記関係で表すグラフである。
To give an overview of the attached drawings, Figure 1 shows the Ay4S
It is a graph showing the reflection spectral characteristics of 1% wave: (nm) (horizontal axis) and the reflectance (coefficient) (vertical axis) of the reflection spectral characteristics of 04. In Figure 2, the spectral sensitivity of A24S104 is determined by the irradiation wavelength (nm) (horizontal axis) and the wavelength 7001111.
1 is a graph expressed in relation to the decrease (coefficient) (vertical axis) of reflectance in No. 1. Figure 3 is a graph showing the reflection spectral characteristics of A45j03 using the above relationship.
It is a graph showing the spectral sensitivity of y281.03 using the above-mentioned interval. Figure 5 (is Q2Sj heat treated at 380℃
It is a graph showing the reflection spectral characteristics of O3 using the above relationship.

第6図は、A72 Si205  の反射分光特性を、
前記関係で表すグラフである。第7図は、Ay2Si2
05  の分光感度を、前記関係で表すグラフである1
、第8図は、680℃で熱処理したA、12Si205
 の反射分光特性を、前記関係で表すグラフである。
Figure 6 shows the reflection spectral characteristics of A72 Si205.
It is a graph expressed by the above-mentioned relationship. Figure 7 shows Ay2Si2
1 which is a graph expressing the spectral sensitivity of 05 using the above relationship.
, Figure 8 shows A,12Si205 heat treated at 680°C.
2 is a graph showing the reflection spectral characteristics of , using the above relationship.

実施例1(Ay4 Sj、04) A24S104は、Ca2SiO4とkyNO3を1=
32のモル比で混合し、白金るつぼに投入し、260℃
で60時間保持12、冷却後、水洗、乾燥1〜で得た。
Example 1 (Ay4 Sj, 04) A24S104 has Ca2SiO4 and kyNO3 of 1=
Mix at a molar ratio of 32, put into a platinum crucible, and heat at 260°C.
After holding for 60 hours at step 12, cooling, washing with water, and drying step 1.

第1図ば、O4SiO+の反射分光特性を示すグラフで
ある。曲線1は、前記のようにして合成後のAy4Si
O4の反射分光特性及び波長550nmの光を約750
mJ/ai照射後、(に20θ℃で30分間υn熱した
後の反射分光特性を示すもので、両者は全く同一である
。そして曲線2は、A24S104に前記のように波長
550nmの光を約乃Om J /crl照射後の反射
分光特性を示す。曲線1と2を比較すると、波長aoo
nmにおける反射率の低下は8優に達し、記録が行われ
ていることを示している。また、この記録後、200℃
、30分間の加熱により反射分光特性が照射前の状態に
復帰することも明らかである3、そして、再度、記録、
消去を繰返すことも可能である。第2図は、八y4S1
.04の分光感度曲線を示(7、縦軸は、300 mJ
lcrl  照射後の波長700nmにおける反射率の
低下幅を示す。波長750nm以下の光で記録が可能な
ことがわかる。記録の読出しには、波長約750 nm
以上の微弱な光源を用い、反射率の差を検出する等の方
法を用いる。
FIG. 1 is a graph showing the reflection spectral characteristics of O4SiO+. Curve 1 shows Ay4Si after synthesis as described above.
Reflection spectral characteristics of O4 and light with a wavelength of 550 nm
It shows the reflection spectral characteristics after mJ/ai irradiation and after heating at 20θ℃ for 30 minutes, and both are exactly the same.Curve 2 shows the reflection spectral characteristics after irradiation with mJ/ai and after heating at 20θ℃ for 30 minutes. It shows the reflection spectral characteristics after irradiation with Om J /crl.Comparing curves 1 and 2, it is found that the wavelength aoo
The decrease in reflectance at nm reaches 8 well, indicating that recording is occurring. Also, after this recording, 200℃
It is also clear that the reflection spectral characteristics return to the state before irradiation by heating for 30 minutes.
It is also possible to repeat the erasure. Figure 2 is 8y4S1
.. The spectral sensitivity curve of 04 is shown (7, the vertical axis is 300 mJ
It shows the decrease in reflectance at a wavelength of 700 nm after lcrl irradiation. It can be seen that recording is possible with light having a wavelength of 750 nm or less. For reading records, a wavelength of approximately 750 nm is used.
A method such as detecting the difference in reflectance using the above-mentioned weak light source is used.

実施例2  (A?z 5iO3) AS12 Sj 03は、BaSiO3とAyNO3を
1:16のモル比で混合し、白金るつぼに投入し、29
0℃で30時間保持し、冷却後、水洗、乾燥しで得だ。
Example 2 (A?z 5iO3) AS12 Sj 03 was prepared by mixing BaSiO3 and AyNO3 at a molar ratio of 1:16, charging the mixture into a platinum crucible, and heating it at 29
It is obtained by keeping at 0°C for 30 hours, cooling, washing with water, and drying.

第3図だおける曲線3は、合成後のA45j03の反射
分光特性を示す6.そして曲@4ば、それに波長450
nmの光をs o m、r/ctrl照射した後の反射
分光特性を示す。波長700nmiCおりる反射率の低
下は13係に達し、可決光により感度良く記録が行われ
ていることを示す6、第4図は、Ay2 Si 03の
分光感度曲線を示し、縦軸は、40m J /cyst
照射後の波長700 nmにおける反射率の低下幅を示
す。この図は、Ay2Si○3が可視光のほぼ全域にわ
たって高い感度を有していることを示している。このA
y2 Sj 03は、加熱すると250℃付近で一旦黒
化し、更に350〜380℃寸で加熱すると、はぼ加熱
前の台に戻る。この」:うに−一度熱処理すると、もは
や室温から380℃以下の温度範囲では、加熱による黒
化は生じない、1熱処理したA、?2Si03も感光性
を示す。第5図゛(おける曲@5は、680℃で熱、処
理)7たΔy2si、03の反射分光特性を示す。そし
て曲線6(d:、380℃で熱処工甲したAg3 Sj
 03に波1i450nmの光を100 mJ /cr
;I  照射し/こ後の反射分光特性を示t。第5図(
−1:、可視ン覧照射1により記録が可能であることを
示(7ている。記録後650℃で60分間の加熱により
、反射分光特性1は、元の曲、線5の状態(・で復)7
、記録、消去を繰返すことも可能である。記録の読出し
には、波長約650 nm以十の微弱な光源を用い、反
射率の差を検出する等の方法を用いろ。
Curve 3 in Figure 3 shows the reflection spectral characteristics of A45j03 after synthesis6. And the song @4ba, and wavelength 450
The reflection spectral characteristics after irradiation with nm light at s o m, r/ctrl are shown. The decrease in reflectance at a wavelength of 700 nmC reached a factor of 13, indicating that recording was carried out with good sensitivity by passing light. 6. Figure 4 shows the spectral sensitivity curve of Ay2Si03, and the vertical axis is 40 m. J/cyst
The graph shows the decrease in reflectance at a wavelength of 700 nm after irradiation. This figure shows that Ay2Si○3 has high sensitivity over almost the entire visible light range. This A
When y2 Sj 03 is heated, it once turns black around 250°C, and when further heated at 350 to 380°C, it returns to its original state before heating. ``This'': Once heat treated, sea urchin no longer darkens due to heating in the temperature range from room temperature to 380℃ or below. 1 Heat treated A, ? 2Si03 also exhibits photosensitivity. Figure 5 shows the reflection spectral characteristics of Δy2si, 03 (song @ 5 was heated and treated at 680° C.). And curve 6 (d: Ag3 Sj heat treated at 380°C
03 wave 1i450nm light 100mJ/cr
;I Indicates the reflection spectral characteristics after irradiation. Figure 5 (
-1: Indicates that recording is possible with visible light irradiation 1 (7). After recording, heating at 650°C for 60 minutes changes the reflection spectral characteristic 1 to the original curve, line 5 state (- 7)
It is also possible to repeat recording and erasing. To read the records, use a method such as using a weak light source with a wavelength of about 650 nm or more and detecting the difference in reflectance.

実施例3  (Af2S]、205) A!jI28i205は、Q −Na、2 Si205
とA、yNO3を1:16のモル比で混合し、白金るつ
ぼに投入し、290℃の温度で48時間保持し、冷却後
水洗、乾燥して得た。ここで、α−Na2 Si205
をβ〜Na25j205又はLj、2 Si205、K
2 Si205、Ba5j、205で代用することはで
きない[V、 F、  ウオトク(V、 F。
Example 3 (Af2S], 205) A! jI28i205 is Q-Na,2Si205
, A, and yNO3 were mixed at a molar ratio of 1:16, put into a platinum crucible, held at a temperature of 290°C for 48 hours, cooled, washed with water, and dried to obtain a mixture. Here, α-Na2Si205
β~Na25j205 or Lj, 2 Si205, K
2 Si205, Ba5j, 205 cannot be substituted [V, F, Otoku (V, F.

Wodtcke )”Z、 anorg、 a、]−1
1g C1]em、  〃−314,p341(196
2)参照〕。a −Na2 Si206ば、Na2CO
3と5102  を1:2のモル比で混合し、810℃
の温度で30時間焼成して調製した。第6図における曲
線7は、合成後のA、2 Siz O5の反射分光特性
を示す。そして曲線8は、それに波長450nmの光を
100 mJ/crl  照射した後の反射分光特性を
示す。波長700nmにおける反射率は9係減少してお
り、記録が行われていることを示している。第7図は、
八% St205の分光感度曲線を示し、縦軸1d、照
射エネルギー100 mJ/ crAで照射後の波長7
00nmKおける反射率の低下幅を示″4−7第7図は
、A+)+251205が可視光のほぼ全域にわたって
感度を有(〜でいることを示して(Aる。
Wodtcke)”Z, anorg, a,]-1
1g C1]em, 〃-314, p341 (196
See 2)]. a -Na2Si206, Na2CO
3 and 5102 were mixed at a molar ratio of 1:2 and heated to 810°C.
It was prepared by firing at a temperature of 30 hours. Curve 7 in FIG. 6 shows the reflection spectral characteristics of A,2SizO5 after synthesis. Curve 8 shows the reflection spectral characteristics after irradiating it with 100 mJ/crl of light with a wavelength of 450 nm. The reflectance at a wavelength of 700 nm decreased by a factor of 9, indicating that recording was being performed. Figure 7 shows
The spectral sensitivity curve of 8% St205 is shown, vertical axis 1d, wavelength 7 after irradiation with irradiation energy 100 mJ/crA.
Figure 7 shows the range of decrease in reflectance at 00 nm K. Figure 7 shows that A+)+251205 has sensitivity over almost the entire range of visible light.

このAg3 Si、205は、加熱するとA % Si
、 03と同様(で250℃付近で一旦黒化し、更に3
50〜380℃才で昇温すると、はぼ加熱前の色に戻る
。このように一度熱処理すると、もはや室温から380
℃寸での温度範囲では、加熱しても黒化は生じない。熱
処理したA y2 S1205  も感光性を示t g
第8図1・ておける曲線9は、380℃で熱処理したA
g35i205 の反射分光特性を示す。そして曲線1
0は、380℃で熱処理したAg3 Si205姥波?
i+450nmの光を100mJ’/rJ照射L7’r
後の反射分光特性を示す。第8図、γよ、可視光照射に
より記録が行えることを示してい乙。記録後360℃で
30分間の加熱により、反射分光特性は、元の曲線9の
状態に復し、記録、消去を繰返すことができる。記録の
読出しには、波長約7DOnm以上の微弱な光源を用い
、反射率の差を検出する等の方法を用いる。
This Ag3Si, 205 becomes A%Si when heated.
, Same as 03 (temporarily blackened at around 250℃, then 3
When the temperature is raised between 50 and 380 degrees Celsius, the color returns to the color before heating. Once heat treated in this way, the temperature will no longer reach 380 degrees from room temperature.
In the temperature range of degrees Celsius, no blackening occurs even when heated. Heat-treated A y2 S1205 also showed photosensitivity t g
Curve 9 in Figure 8 1 shows A heat-treated at 380°C.
The reflection spectral characteristics of g35i205 are shown. and curve 1
0 is Ag3 Si205 Ubanami heat treated at 380℃?
i+450nm light 100mJ'/rJ irradiation L7'r
Shows the later reflection spectral characteristics. Figure 8, γ, shows that recording can be performed by visible light irradiation. By heating at 360° C. for 30 minutes after recording, the reflection spectral characteristics return to the original state of curve 9, and recording and erasing can be repeated. To read the record, a method such as using a weak light source with a wavelength of about 7 DO nm or more and detecting a difference in reflectance is used.

以上の各実施例から明らかなように、本発明の光学記録
材料、け、既述の各種の利点を有し、顕著な効果を奏す
るものである。
As is clear from the above examples, the optical recording material of the present invention has the various advantages described above and exhibits remarkable effects.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は、Ay4Sj、04の反射分光特性全、波長と
反射率との関係で表すクラスである。第2図’d 、A
g3 s]、 o4の分光感度を、照射波長と光照射に
よる波1%7[]0nmKおける反射率の低下との関係
で表すグラフである。第6図け、Ay2S103の反射
分光特性を、前記関係で表すグラフ、第4図は、A y
2 Sl 03の分光感度を、前記関係で表すグラフ、
第5図は、380℃で熱処理!、たA72S103 の
反射分光特性を、前記関係で表すグラフ、第6図は、A
g38120s の反射分光特性を、前記関係で表すグ
ラフ、第7図は、AP25j206の分光感度を、前記
関係で表すグラフ、第8図は、380℃で熱処理したA
Sl125i205の反射分光特性を、前記関係で表す
グラフである。 特許出願人 日本電信電話公社 代理人 中 本  宏 第 l 図 波長 (nmン 第2図 u6射波長(nm) 第 3 図 波長(4m) 第4図 照射波長(nm) 第 、5′  図 波長(nwr) 第 6 図 波長(nm) 第 7 図 照射波長((rm) 第3図 波長(nrn ) 手続補正書(自発補正) 昭和57年10月1 日 特許庁長官  若 杉 和 夫 殿 1、事件の表示  昭和56年特許願第184496号
2、発明の名称  光学記録材料 5、補正をする者 事件との関係  特許出願人 住 所   東京都千代田区内幸町1丁目1番6号名 
称  (422’)日本電信電話公社代表者  真 藤
   恒 西新橋中央ビル302号 電話(437)−3467 氏  名   弁理士(7850)  中  本   
 宏5、補正命令の日付 (自発補正) &補正の対象 (1)  明細書の発明の詳細な説明の欄l補正の内容 明細書の発明の詳細な説明の欄を下記のとおり補正する
。 (1)明細書第2頁9行の「定着」を1現像Jと補正す
る。 (2)  同第3頁13行の1定着」を「現像」と補正
する。
FIG. 1 shows all the reflection spectral characteristics of Ay4Sj, 04, and the class represented by the relationship between wavelength and reflectance. Figure 2'd, A
3 is a graph showing the spectral sensitivity of o4 in terms of the relationship between the irradiation wavelength and the decrease in reflectance at a wavelength of 1%7[]0 nmK due to light irradiation. Figure 6 is a graph showing the reflection spectral characteristics of Ay2S103 using the above relationship.
2 A graph representing the spectral sensitivity of Sl 03 using the above relationship,
Figure 5 shows heat treatment at 380℃! A graph showing the reflection spectral characteristics of A72S103 using the above relationship, FIG.
Fig. 7 is a graph showing the spectral sensitivity of AP25j206 using the above relationship, and Fig. 8 is a graph showing the reflection spectral characteristics of AP25j206 using the above relationship.
It is a graph showing the reflection spectral characteristics of Sl125i205 using the above relationship. Patent applicant Hiroki Nakamoto, agent for Nippon Telegraph and Telephone Public Corporation Figure wavelength (nm) Figure 2 U6 radiation wavelength (nm) Figure 3 Wavelength (4m) Figure 4 Irradiation wavelength (nm) Figure 4 Wavelength (nm) nwr) Figure 6 Wavelength (nm) Figure 7 Irradiation wavelength ((rm) Figure 3 Wavelength (nrn) Procedural amendment (voluntary amendment) October 1, 1981 Kazuo Wakasugi, Commissioner of the Patent Office, Case 1 Indication: 1984 Patent Application No. 184496 2, Title of the invention: Optical recording material 5, Relationship to the case of the person making the amendment Patent applicant address: 1-1-6 Uchisaiwai-cho, Chiyoda-ku, Tokyo
Name (422') Nippon Telegraph and Telephone Public Corporation Representative Makoto Fuji Tsuneishi Shinbashi Chuo Building 302 Telephone (437)-3467 Name Patent Attorney (7850) Nakamoto
Hiroshi 5, Date of amendment order (voluntary amendment) & Subject of amendment (1) Detailed explanation of the invention column in the specification l Contents of amendment The detailed explanation of the invention column in the specification is amended as follows. (1) "Fixing" on page 2, line 9 of the specification is corrected to 1 development J. (2) Correct "1 fixing" on page 3, line 13 of the same page to "developing."

Claims (1)

【特許請求の範囲】 t  Ayz05102系の化合物で構成することを特
徴とする光学記録材料。 2 該化合物が、Aグ4Si○4、Ay2SiO3及び
Aグ。 3i205  よりなる群から選釈した化合物である特
許請求の範囲第1項に記載の光学記録材料。
[Scope of Claims] An optical recording material characterized by comprising a tAyz05102-based compound. 2 The compounds are Ag4Si○4, Ay2SiO3 and Ag. The optical recording material according to claim 1, which is a compound selected from the group consisting of 3i205.
JP56184496A 1981-11-19 1981-11-19 Optical recording material Granted JPS5887183A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56184496A JPS5887183A (en) 1981-11-19 1981-11-19 Optical recording material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56184496A JPS5887183A (en) 1981-11-19 1981-11-19 Optical recording material

Publications (2)

Publication Number Publication Date
JPS5887183A true JPS5887183A (en) 1983-05-24
JPS6356920B2 JPS6356920B2 (en) 1988-11-09

Family

ID=16154194

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56184496A Granted JPS5887183A (en) 1981-11-19 1981-11-19 Optical recording material

Country Status (1)

Country Link
JP (1) JPS5887183A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5401609A (en) * 1991-12-13 1995-03-28 Tdk Corporation Optical recording medium and its production
CN103372431A (en) * 2012-04-25 2013-10-30 三星电子株式会社 Visible light sensitive photocatalyst, method of producing visible light sensitive photocatalyst, and electrochemical water decomposition cell and organic material decomposition system each including visible light sensitive photocatalyst

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5401609A (en) * 1991-12-13 1995-03-28 Tdk Corporation Optical recording medium and its production
CN103372431A (en) * 2012-04-25 2013-10-30 三星电子株式会社 Visible light sensitive photocatalyst, method of producing visible light sensitive photocatalyst, and electrochemical water decomposition cell and organic material decomposition system each including visible light sensitive photocatalyst
CN103372431B (en) * 2012-04-25 2017-05-24 三星电子株式会社 Visible light sensitive photocatalyst, method of producing visible light sensitive photocatalyst, and electrochemical water decomposition cell and organic material decomposition system each including visible light sensitive photocatalyst

Also Published As

Publication number Publication date
JPS6356920B2 (en) 1988-11-09

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