JPS61201639A - Plate lens - Google Patents
Plate lensInfo
- Publication number
- JPS61201639A JPS61201639A JP60043530A JP4353085A JPS61201639A JP S61201639 A JPS61201639 A JP S61201639A JP 60043530 A JP60043530 A JP 60043530A JP 4353085 A JP4353085 A JP 4353085A JP S61201639 A JPS61201639 A JP S61201639A
- Authority
- JP
- Japan
- Prior art keywords
- glass
- lens
- substrate
- ions
- mol
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C21/00—Treatment of glass, not in the form of fibres or filaments, by diffusing ions or metals in the surface
- C03C21/001—Treatment of glass, not in the form of fibres or filaments, by diffusing ions or metals in the surface in liquid phase, e.g. molten salts, solutions
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/078—Glass compositions containing silica with 40% to 90% silica, by weight containing an oxide of a divalent metal, e.g. an oxide of zinc
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/083—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
- C03C3/091—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Automatic Focus Adjustment (AREA)
- Surface Treatment Of Glass (AREA)
- Glass Compositions (AREA)
Abstract
Description
【発明の詳細な説明】 〔産業上の利用分野〕 一体的に形成した平板レンズに関する。[Detailed description of the invention] [Industrial application field] The present invention relates to an integrally formed flat plate lens.
多数の屈折率分布型レンズを平面的に配列したレンズア
レイは、複写機の光学系、半導体レーザ上記のレンズア
レイは、屈折率が中心軸上で最大で周辺に向けてパラポ
リツクに減少する分布をもつ円柱レンズを多数集束した
ものであるが、かかるレンズアレイと同等の機能をもち
、しかも極めて微小なレンズを非常に多数集積化できる
レンズに、光軸が基板面に垂直であり、屈折率が光軸か
ら周辺に向けておよび光軸方向にほぼパラポリツクな形
状で減少する分布をもつ屈折率勾配型レンズ2を基板と
一体的に形成したものであり、第2図のような円形レン
ズアレイ、あるいは第3図に示すようなライン状レンズ
アレイ等がある。Lens arrays, in which a large number of graded refractive index lenses are arranged in a plane, are used in the optical system of copying machines and semiconductor lasers. This lens has the same function as such a lens array, and can integrate a large number of extremely small lenses. A gradient refractive index lens 2 having a distribution that decreases from the optical axis toward the periphery and in an almost parapolitan shape in the optical axis direction is formed integrally with the substrate, and is a circular lens array as shown in FIG. Alternatively, there is a linear lens array as shown in FIG.
上記のような平板レンズを製造するには、第v図に示す
ように、NaあるいはKなどの電子分極率の比較的低い
1価のイオンを含む平板ガラスから成る基板lの片面上
に、開口3を所定のレンズアレイパターンで設けた金属
マスフグを施し、このマスク面に、Tlイオン、Agイ
オンなどガラスの屈折率増大に寄与の大きい陽イオンを
含む溶融塩を接触させ、直流電圧を基板両面間に印加し
つつあるいは自然拡散でマスク開口を通して溶融塩中の
上記イオンよとガラス中の前記イオンとを交換させ、ガ
ラス中に拡散したイオンの濃度分布に応じた屈折率分布
を基板内に形成させる。In order to manufacture the above-mentioned flat plate lens, as shown in FIG. 3 is applied with a metal masking mask provided with a predetermined lens array pattern, a molten salt containing cations such as Tl ions and Ag ions that greatly contribute to increasing the refractive index of glass is brought into contact with the mask surface, and a DC voltage is applied to both sides of the substrate. The above-mentioned ions in the molten salt are exchanged with the above-mentioned ions in the glass through the mask opening while applying an electric current or by natural diffusion, and a refractive index distribution corresponding to the concentration distribution of the ions diffused into the glass is formed in the substrate. let
そして、上記のようなイオン交換法で平板レンズを製作
する場合の基板ガラスとしては、例えば特開昭j’7−
!;3702号公報には、モル%で5i0275.0%
+ B2O3/ 0.2%、Bad(7,7%、Na2
O9,6%*に204(、r%の組成を有するガラス(
BK−7光学ガラス)が例示されている。For example, as a substrate glass for manufacturing a flat lens by the above-mentioned ion exchange method,
! ;3702 publication contains 5i0275.0% in mol%
+ B2O3/ 0.2%, Bad (7,7%, Na2
Glass with a composition of O9,6%* to 204(,r%)
BK-7 optical glass) is exemplified.
上記のようにマスキングを施した基板ガラスを溶融塩に
接触させてイオン拡散で屈折率勾配型レンズを基板内に
形成する場合、溶融塩の温度がg o o”c以上の高
温でしかも数十時間という長時間にわたり浸漬処理を行
なうため、基板ガラス表面が溶融塩によって侵食を受け
たり、または母材ガラスの僅かの組成変動あるいは溶融
塩の組成変動によってガラス表面に失う物が生成され、
場合によっては基板ガラス全体が結晶化するという問題
があった。このような失透あるいは侵食をガラス表面に
生じるとガラス中へのイオンの拡散が不均一になりやす
く、安定した光学性能をもつレンズが得られなくなる。When a masked substrate glass is brought into contact with a molten salt as described above and a refractive index gradient lens is formed in the substrate by ion diffusion, the temperature of the molten salt is higher than g Because the immersion process is carried out over a long period of time, the substrate glass surface may be eroded by the molten salt, or substances may be generated on the glass surface due to slight compositional fluctuations in the base material glass or compositional fluctuations in the molten salt.
In some cases, there was a problem that the entire substrate glass was crystallized. When such devitrification or erosion occurs on the glass surface, ions tend to diffuse unevenly into the glass, making it impossible to obtain a lens with stable optical performance.
主要成分として、5io2:us−ざ0%(単位モル%
、以下間)、アルカリ金属酸化物(R20) :ざ〜3
幻G r ZnO’ 2〜20 ’IA + B 20
3 ’ 0〜Ir AJ 203 ’ 0〜7%、Zr
O:0〜r% 、CaO+BaO+MgO: 0〜10
% を含有するガラスを平板レンズの基板ガラスとして
使用する。上記主要成分以外にS rOr P b O
t T 102 + L a 203 rSb203+
AS20:s等の添加物を少量含有することができる。As a main component, 5io2:us-za0% (unit: mol%)
, below), alkali metal oxide (R20): Za~3
Phantom G r ZnO' 2~20 'IA + B 20
3' 0~Ir AJ 203' 0~7%, Zr
O: 0~r%, CaO+BaO+MgO: 0~10
% is used as a substrate glass for a flat lens. In addition to the above main components, S rOr P b O
t T 102 + L a 203 rSb203+
A small amount of additives such as AS20:s may be included.
以下本発明に係るガラス組成の各成分について詳述する
と、S 102はガラスの骨格となる成分であり、75
%未満ではガラスの耐久性、安定性が減少し、ざ0%を
越えると溶融温度が上昇し、また他の構成成分の必要量
が確保されず大きな屈折率差をもつレンズが得られなく
なるのでl〜1OtI、の範囲内とすることが必要であ
り、さらに53〜75%の範囲内が好ましい。B2O3
は添加することによってガラスの溶解が容易になるが、
あまり多量に入れると揮発による脈理が発生したり、イ
オン交換によってレンズ部分の変形が生じたりするので
、含有量の範囲はOSざ%とする。znOはガラス化範
る影響が他の二価の修飾酸化物に比べて小さい。Each component of the glass composition according to the present invention will be described in detail below. S102 is a component that forms the skeleton of the glass, and 75
If it is less than 0%, the durability and stability of the glass will decrease, and if it exceeds 0%, the melting temperature will rise, and the necessary amounts of other components will not be secured, making it impossible to obtain a lens with a large refractive index difference. It is necessary to set it within the range of 1 to 1 OtI, and more preferably within the range of 53 to 75%. B2O3
Adding molten glass makes it easier to melt the glass, but
If too much is added, striae may occur due to volatilization or deformation of the lens portion may occur due to ion exchange, so the content should be within the range of OS %. ZnO has a smaller effect on vitrification than other divalent modified oxides.
ただし2%未満ではガラスの失透性、耐久性が悪くなり
、また20%を越えても耐久性が悪くなるので2−JO
%の範囲内とすることが必要であり、さらに5〜75%
の範囲内が望ましい。ZrO2はガラスの耐候性を向上
させる効果がきわめて大であるが、2%を越えると不溶
解を生じやすくなるので、その含有量範囲は0〜2%で
ある。AA!203はZrO2と同様ガラスの耐候性、
イオン交換時の耐溶融塩性向上に奇与するが、7%を越
えると溶解性を悪化させるので0〜7%の範囲内とする
ことが必要であり、さらに0〜7%の範囲内が望ましい
。However, if it is less than 2%, the devitrification and durability of the glass will be poor, and if it exceeds 20%, the durability will be poor, so 2-JO
It is necessary to keep it within the range of 5% to 75%.
It is desirable to be within the range of . ZrO2 has a very large effect on improving the weather resistance of glass, but if it exceeds 2%, it tends to become insoluble, so its content ranges from 0 to 2%. AA! 203 has the same weather resistance as ZrO2,
It contributes to the improvement of molten salt resistance during ion exchange, but if it exceeds 7%, the solubility deteriorates, so it is necessary to keep it within the range of 0 to 7%. desirable.
CaO*MgO,BaOはガラス化範囲を広げガラスの
耐久性向上に奇与し、これらの合計量で0〜10%の範
囲内で含有させることができる。CaO*MgO and BaO extend the range of vitrification and improve the durability of the glass, and can be contained in a total amount of 0 to 10%.
本発明において最も重要なガラス成分は1価のアルカリ
金属酸化物(Rho)である。前述したように、イオン
交換法で平板レンズを製作する方法では、基板ガラス中
に含まれる電子分極率の比較的低い1価のイオンと、T
Jイオン、Agイオンなど電子分極率の大きいイオンと
を部分的に交換させてその部分に屈折率分布を形成し、
アルカリ金属酸化物(以下R20と略記する)上記の交
換イオンとしての機能をもつ。そしてR20がf%未満
では形成されるレンズの開口角(θ)が小さくなって実
用的でなく、また含有量が3j%を越えるとガラスの耐
久性が急激に悪化するので、R20の合計量は1%〜3
5%の範囲内であることが必要であり、好ましい範囲は
12^J、r%である。The most important glass component in the present invention is a monovalent alkali metal oxide (Rho). As mentioned above, in the method of manufacturing a flat lens using the ion exchange method, monovalent ions with relatively low electronic polarizability contained in the substrate glass and T
By partially exchanging ions with high electronic polarizability such as J ions and Ag ions, a refractive index distribution is formed in that part,
Alkali metal oxide (hereinafter abbreviated as R20) has a function as the above-mentioned exchange ion. If the R20 content is less than f%, the aperture angle (θ) of the formed lens will become small, making it impractical, and if the content exceeds 3j%, the durability of the glass will deteriorate rapidly, so the total amount of R20 is 1% to 3
It is necessary to be within a range of 5%, and a preferable range is 12^J, r%.
Rとしては、レンズの最大屈折率差Δnを大きくするに
はbi 、 uaが効果的であり、イオン半径の大きい
Tlイオンとの交換におけるガラス構造へのストレスを
考えるとKl(38が好ましい。したがって平板レンズ
の基板ガラス組成としては、L l m IJaのうち
の一種以上およびKIO3のうちの一種以上を前述した
合計量範囲内で含有させることが望ましい。As for R, bi and ua are effective in increasing the maximum refractive index difference Δn of the lens, and considering the stress on the glass structure during exchange with Tl ions having a large ionic radius, Kl (38 is preferable. Therefore As for the substrate glass composition of the flat plate lens, it is desirable to contain one or more of L l m IJa and one or more of KIO3 within the above-mentioned total amount range.
本発明に係るガラス組成として、上記成分以外K Sr
O、PbOI TiO2t La2O3から選んだ一種
または二種以上の成分を合計量で5%以下の範囲で含有
させることができる。これら成分はガラス化範囲の拡大
とガラスの溶解性向上のために効果があるが、上記範囲
を越えて多量に入れるとイオン交換が円滑に進行しにく
くなる。As the glass composition according to the present invention, in addition to the above components, K Sr
One or more components selected from O, PbOI, TiO2t, La2O3 can be contained in a total amount of 5% or less. These components are effective in expanding the vitrification range and improving the solubility of glass, but if added in amounts exceeding the above range, ion exchange will be difficult to proceed smoothly.
さらに本発明に係るガラスは、ガラス溶解時の清面剤と
して使用される5b2o3やASg03を003%以下
の範囲で含有していてよい。Further, the glass according to the present invention may contain 5b2o3 or ASg03, which is used as a surface cleaning agent during glass melting, in a range of 0.003% or less.
第1表に示した各組成成分の原料として、珪石粉、ホウ
酸、酸化亜鉛、炭酸カリウム、炭酸ナトリウム、酸化ジ
ルコニウム、水酸化アルミニウム、酸化アンチモンある
いは無水亜砒酸を用い、これらの原料の所定量を混合し
て得た調合物を白金ルツボに入れ、1xzo〜1soo
℃の電気炉内で溶融し、良く攪拌してガラスを均質にし
た後1ooo−irs。Silica powder, boric acid, zinc oxide, potassium carbonate, sodium carbonate, zirconium oxide, aluminum hydroxide, antimony oxide, or arsenous anhydride are used as raw materials for each composition shown in Table 1, and predetermined amounts of these raw materials are Put the mixture obtained by mixing into a platinum crucible and add 1xzo to 1soo.
1ooo-irs after melting in an electric furnace at ℃ and stirring well to make the glass homogeneous.
°Cでモールドに流し込み、徐冷して第1表に示したガ
ラスを得た。It was poured into a mold at °C and slowly cooled to obtain the glass shown in Table 1.
上記のようにして作成したガラス板をjQtas角で厚
さjmに光学研磨して基板とし、この基板の片面にイオ
ン透過防止マスクとして金属チタン膜を施し、このチタ
ン膜に通常の7オトリソグラフイー技術を用いて、円形
のイオン透過用開口部を設けた。この開口径は実施例1
の場合で約1100ttである。このマスキングを施し
たガラス基板を、硫酸タリウム(TA’2SO4) 6
0モル%と硫酸亜鉛(ZnSO4) 90モル%の混合
溶融塩中に浸漬してイオン交換処理を行なった。このと
きの溶融塩温度は第1表の各ガラスの転移点よりも約i
o″C高い温度としている。The glass plate prepared as described above is optically polished to a thickness of jm at a jQtas angle to form a substrate.A metallic titanium film is applied to one side of this substrate as a mask for preventing ion transmission, and this titanium film is subjected to ordinary 7 otolithography. A circular ion permeation opening was created using the technique. This opening diameter is as shown in Example 1.
In this case, it is approximately 1100 tt. This masked glass substrate was then coated with thallium sulfate (TA'2SO4) 6
An ion exchange treatment was performed by immersing it in a mixed molten salt of 0 mol % and 90 mol % zinc sulfate (ZnSO4). The molten salt temperature at this time is about i below the transition point of each glass in Table 1.
o″C high temperature.
また、比較例として、従来平板レンズの基板ガラスに用
いられているBK−7光学ガラスの基板を作製して上述
と同様にしてイオン交換処理を行なった。イオン交換処
理に際−して、本願の実施例11≠、3と比較例につい
ては基板の両面間に約30Vの直流電界を印加し、他は
電界印加せず自然拡散で処理した。Further, as a comparative example, a substrate of BK-7 optical glass, which is conventionally used as a substrate glass for flat lenses, was prepared and subjected to ion exchange treatment in the same manner as described above. During the ion exchange treatment, a DC electric field of approximately 30 V was applied between both surfaces of the substrates for Examples 11≠ and 3 of the present application and Comparative Example, and for the others, natural diffusion was performed without applying an electric field.
イオン交換処理を終了後表面のマスクを除去して、基板
内に形成されている屈折率勾配レンズのレンズ径と開口
数(NA)を測定した。その結果を第1表の下段に示す
。After the ion exchange treatment was completed, the mask on the surface was removed, and the lens diameter and numerical aperture (NA) of the refractive index gradient lens formed within the substrate were measured. The results are shown in the lower part of Table 1.
得られた実施例7〜乙の平板レンズはいずれもガラス表
面に失透物や侵蝕が全く認められず高透明であった。こ
れに対して比較例のBK−7ガラスによるものはガラス
表面に溶融塩の侵蝕による薄い白濁を生じていた。The obtained planar lenses of Examples 7 to B were all highly transparent with no devitrification or corrosion observed on the glass surface. On the other hand, in the case of the comparative example made of BK-7 glass, a slight cloudiness was produced on the glass surface due to the erosion of the molten salt.
また、レンズ径が等しい実施例よと比較例とを比べても
明らかなように、本願発明に係るガラスを基板として用
いた平板レンズは、径が7m以下の非常に小さいレンズ
であっても充分に大きな開口数が得られる。Furthermore, as is clear from comparing the Example and Comparative Example with the same lens diameter, the flat lens using the glass according to the present invention as a substrate is sufficient even for a very small lens with a diameter of 7 m or less. A large numerical aperture can be obtained.
本発明によれば、溶融塩との接触によるイオン交換処理
時におけるレンズ基板ガラスの侵食がほとんど無くなり
、光学的に安定した性能のレンズが得られると同時に、
小口径でしかも開口数(NA)が大きいレンズが得られ
る。According to the present invention, erosion of the lens substrate glass during ion exchange treatment due to contact with molten salt is almost eliminated, and at the same time, a lens with optically stable performance is obtained.
A lens with a small diameter and a large numerical aperture (NA) can be obtained.
また、使用時においても従来のBK−7光学ガラスと同
等以上の耐候性を有していることが確められている。Furthermore, it has been confirmed that it has weather resistance equivalent to or better than conventional BK-7 optical glass even when used.
第1図は平板レンズの側断面図、第2図は平板レンズの
レンズ形状の一例を示す平面図、第3図は他のレンズ形
状例を示す平面図、第ψ図は平板レンズの製法の一例を
示す断面図である。Figure 1 is a side sectional view of a flat plate lens, Figure 2 is a plan view showing an example of the lens shape of the flat lens, Figure 3 is a plan view showing other examples of lens shapes, and Figure ψ is a method for manufacturing the flat lens. It is a sectional view showing an example.
Claims (1)
光軸から周辺に向けておよび光軸方向に変化する分布を
もつレンズ部分を一体に形成した平板レンズにおいて、
前記基板ガラスは主要成分として、SiO_2:45〜
80モル%、アルカリ金属酸化物(R_2O):8〜3
5モル%、ZnO:2〜20モル%、B_2O_3:0
〜8モル%、Al_2O_3:0〜7モル%、ZrO_
2:0〜2モル%、CaO+BaO+MgO:0〜10
モル%を含有することを特徴とする平板レンズ。In a flat lens in which a glass substrate is integrally formed with a lens portion whose optical axis is perpendicular to the substrate surface and whose refractive index has a distribution that changes from the optical axis toward the periphery and in the optical axis direction,
The main component of the substrate glass is SiO_2:45~
80 mol%, alkali metal oxide (R_2O): 8-3
5 mol%, ZnO: 2 to 20 mol%, B_2O_3:0
~8 mol%, Al_2O_3: 0-7 mol%, ZrO_
2: 0-2 mol%, CaO+BaO+MgO: 0-10
A flat lens characterized by containing mol%.
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60043530A JPS61201639A (en) | 1985-03-05 | 1985-03-05 | Plate lens |
DE19863607259 DE3607259A1 (en) | 1985-03-05 | 1986-03-05 | MICRO LENS PLATE AND METHOD FOR THEIR PRODUCTION |
FR868603088A FR2578658B1 (en) | 1985-03-05 | 1986-03-05 | MICROLENTINE PLATE AND MANUFACTURING METHOD THEREOF |
GB8605371A GB2173915B (en) | 1985-03-05 | 1986-03-05 | Plate microlens having gradient index lenses and manufacture thereof |
US07/317,079 US4952037A (en) | 1985-03-05 | 1989-02-28 | Plate microlens and method for manufacturing the same |
US07/616,734 US5104435A (en) | 1985-03-05 | 1990-11-21 | Method of making a plate microlens |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60043530A JPS61201639A (en) | 1985-03-05 | 1985-03-05 | Plate lens |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61201639A true JPS61201639A (en) | 1986-09-06 |
JPH0364460B2 JPH0364460B2 (en) | 1991-10-07 |
Family
ID=12666297
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60043530A Granted JPS61201639A (en) | 1985-03-05 | 1985-03-05 | Plate lens |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61201639A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0253001U (en) * | 1988-10-06 | 1990-04-17 | ||
US6816319B2 (en) | 2002-02-22 | 2004-11-09 | Nippon Sheet Glass Co., Ltd. | Planar lens |
JP2011507038A (en) * | 2007-12-21 | 2011-03-03 | オスラム オプト セミコンダクターズ ゲゼルシャフト ミット ベシュレンクテル ハフツング | Optoelectronic device and image recording device |
JP2013177298A (en) * | 2007-08-03 | 2013-09-09 | Nippon Electric Glass Co Ltd | Tempered glass substrate and method of producing the same |
JP2014510012A (en) * | 2011-03-16 | 2014-04-24 | アップル インコーポレイテッド | Controlled chemical strengthening of thin glass |
-
1985
- 1985-03-05 JP JP60043530A patent/JPS61201639A/en active Granted
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0253001U (en) * | 1988-10-06 | 1990-04-17 | ||
US6816319B2 (en) | 2002-02-22 | 2004-11-09 | Nippon Sheet Glass Co., Ltd. | Planar lens |
JP2013177298A (en) * | 2007-08-03 | 2013-09-09 | Nippon Electric Glass Co Ltd | Tempered glass substrate and method of producing the same |
JP2011507038A (en) * | 2007-12-21 | 2011-03-03 | オスラム オプト セミコンダクターズ ゲゼルシャフト ミット ベシュレンクテル ハフツング | Optoelectronic device and image recording device |
JP2014510012A (en) * | 2011-03-16 | 2014-04-24 | アップル インコーポレイテッド | Controlled chemical strengthening of thin glass |
Also Published As
Publication number | Publication date |
---|---|
JPH0364460B2 (en) | 1991-10-07 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EXPY | Cancellation because of completion of term |