JP2717702B2 - Optical element - Google Patents
Optical elementInfo
- Publication number
- JP2717702B2 JP2717702B2 JP1117119A JP11711989A JP2717702B2 JP 2717702 B2 JP2717702 B2 JP 2717702B2 JP 1117119 A JP1117119 A JP 1117119A JP 11711989 A JP11711989 A JP 11711989A JP 2717702 B2 JP2717702 B2 JP 2717702B2
- Authority
- JP
- Japan
- Prior art keywords
- prism
- refractive index
- index layer
- optical element
- optical
- 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 - Fee Related
Links
- 230000003287 optical effect Effects 0.000 title claims description 21
- 239000000853 adhesive Substances 0.000 claims description 14
- 230000001070 adhesive effect Effects 0.000 claims description 14
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 5
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
- 238000005304 joining Methods 0.000 claims description 4
- MMKQUGHLEMYQSG-UHFFFAOYSA-N oxygen(2-);praseodymium(3+) Chemical compound [O-2].[O-2].[O-2].[Pr+3].[Pr+3] MMKQUGHLEMYQSG-UHFFFAOYSA-N 0.000 claims description 3
- 229910003447 praseodymium oxide Inorganic materials 0.000 claims description 3
- ORUIBWPALBXDOA-UHFFFAOYSA-L magnesium fluoride Chemical compound [F-].[F-].[Mg+2] ORUIBWPALBXDOA-UHFFFAOYSA-L 0.000 claims description 2
- 229910001635 magnesium fluoride Inorganic materials 0.000 claims description 2
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 25
- 239000010408 film Substances 0.000 description 13
- 239000000126 substance Substances 0.000 description 9
- 238000007740 vapor deposition Methods 0.000 description 8
- 238000002834 transmittance Methods 0.000 description 7
- 238000000151 deposition Methods 0.000 description 5
- 239000012788 optical film Substances 0.000 description 5
- 229910004298 SiO 2 Inorganic materials 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000003595 spectral effect Effects 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- 229910010413 TiO 2 Inorganic materials 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- 229910001882 dioxygen Inorganic materials 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 229910052777 Praseodymium Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000007767 bonding agent Substances 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 238000013500 data storage Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 238000010884 ion-beam technique Methods 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000005240 physical vapour deposition Methods 0.000 description 1
- PUDIUYLPXJFUGB-UHFFFAOYSA-N praseodymium atom Chemical compound [Pr] PUDIUYLPXJFUGB-UHFFFAOYSA-N 0.000 description 1
- 239000012495 reaction gas Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000000411 transmission spectrum Methods 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Landscapes
- Optical Elements Other Than Lenses (AREA)
- Polarising Elements (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、光学メモリヘッドや、カラー複写機、TVプ
ロジェクション装置に用いられる各種のプリズム形状を
有するビームスプリッタに関する。Description: TECHNICAL FIELD The present invention relates to a beam splitter having various prism shapes used for an optical memory head, a color copying machine, and a TV projection device.
近年、大容量のデータ記憶装置の必要性が高まり、光
ディスク装置、光磁気ディスク装置などが多く利用され
るようになっている。これらの装置では、光学ヘッドを
使用してデータを読み取っている。この光学ヘッドの中
にビームスプリッタが使用されており、該光学ヘッドは
例えば所定形状に加工されたプリズムの一面に、高屈折
率の誘電体物質と低屈折率の誘電体物質とが真空蒸着等
により交互に積層された積層光学膜を形状する。その
後、このプリズムと別のプリズムとを接着剤を用いて接
合してビームスプリッタとする。In recent years, the need for large-capacity data storage devices has increased, and optical disk devices, magneto-optical disk devices, and the like have been widely used. In these devices, data is read using an optical head. A beam splitter is used in the optical head. For example, a high refractive index dielectric substance and a low refractive index dielectric substance are vacuum-deposited on one surface of a prism processed into a predetermined shape. To form the laminated optical films alternately laminated. Thereafter, this prism and another prism are joined with an adhesive to form a beam splitter.
2つのプリズムを接合するために用いられる接合剤と
して熱硬化型と紫外線硬化型の2種類がある。この2種
の接着剤を作業性、生産効率の点から比較してみると、
まず熱硬化型接着剤は、 1)2つのプリズム間に介在した熱硬化型接着剤は加
圧、加熱されることにより、接着剤の粘度が低くなりプ
リズムと接着治具との間に流込み、プリズムと接着治具
とが接着されて、取外しが困難であるばかりか、プリズ
ムが破損することもある、 2)治具で2つのプリズムを位置合せした状態で加熱す
るため、治具に熱応力、熱膨張が発生し、プリズム相互
の位置ずれを起し易い、 3)接着時に気泡等が発生すると再生が困難である、 4)接着剤の種類により多少異なるが、一般的に紫外線
硬化型に比べ硬化時間を長く必要とする、 という欠点を持つ。As a bonding agent used for bonding the two prisms, there are two types, a thermosetting type and an ultraviolet setting type. Comparing these two types of adhesives in terms of workability and production efficiency,
First, the thermosetting adhesive is as follows: 1) The thermosetting adhesive interposed between the two prisms is pressurized and heated to lower the viscosity of the adhesive and flow between the prism and the bonding jig. The prism and the bonding jig are adhered to each other, so that not only is the removal difficult, but the prism may be damaged. 2) The jig is heated while the two prisms are aligned with each other. Stress and thermal expansion occur, which tends to cause misalignment between prisms. 3) Reproduction is difficult if bubbles or the like are generated during bonding. 4) Although it differs slightly depending on the type of adhesive, it is generally an ultraviolet curing type. It has the disadvantage of requiring a longer curing time than that of.
これに対し、紫外線硬化型接着剤は次にような長所を
もつ。On the other hand, the ultraviolet curable adhesive has the following advantages.
1)仮固定(数秒〜10数秒の紫外線照射)の状態で接着
治具から偏光ビームスプリッタを取出すため、取外しが
容易でありプリズムの破損が少ない。1) Since the polarizing beam splitter is taken out of the bonding jig in a temporarily fixed state (irradiation of ultraviolet light for several seconds to several tens of seconds), the polarizing beam splitter is easily detached and the prism is hardly damaged.
2)接着治具を加熱する必要がない為、プリズム相互の
位置ずれが起こりにくい。2) Since there is no need to heat the bonding jig, misalignment between the prisms hardly occurs.
仮固定の状態で位置ずれ、気泡の発生時の検査が可能
であり、仮に位置ずれ、気泡が発生しても容易に再生す
ることができる。Inspection at the time of positional deviation and generation of bubbles is possible in the temporarily fixed state, and even if positional deviation and generation of bubbles occur, reproduction can be easily performed.
3)接着治具は、仮固定までしか使わないため、治具の
回転効率が高い。3) Since the bonding jig is used only for temporary fixing, the rotation efficiency of the jig is high.
以上のように、量産という面からみると、紫外線硬化
型接着剤の方が、圧倒的に有利である。しかし、紫外線
を用いて接合を行なうと、積層膜の特性が大きく変化し
てしまうという欠点がある。特に、高屈折率物質に酸化
チタニウムを使用した場合顕著である。As described above, from the viewpoint of mass production, the ultraviolet curable adhesive is overwhelmingly advantageous. However, when the bonding is performed using ultraviolet rays, there is a disadvantage that the characteristics of the laminated film are greatly changed. In particular, this is remarkable when titanium oxide is used as the high refractive index substance.
第7図に45゜入射の偏光ビームスプリッタの例とし
て、プリズム材質をBK7、低屈折率物質として二酸化珪
素、高屈折率物質として酸化チタニウムを用いた偏光ビ
ームスプリッタの特性を示す。FIG. 7 shows the characteristics of a polarizing beam splitter using BK7 as a prism material, silicon dioxide as a low-refractive-index substance, and titanium oxide as a high-refractive-index substance as an example of a 45 ° incident polarizing beam splitter.
曲線(a)で仮固定後、曲線(b)で本硬化後の特性
を示す。Curve (a) shows the characteristics after temporary fixing, and curve (b) shows the characteristics after full curing.
図より明らかに両波の透過率が本硬化後(接合完了
後)劣化していることがわかる。It is apparent from the figure that the transmittance of both waves is deteriorated after the main curing (after the completion of the joining).
本発明の目的は、量産上の作業性、効率に優れた紫外
線硬化型接着剤を用いる接合法により特性が損なわれる
ことのない積層光学膜を提供することにある。SUMMARY OF THE INVENTION An object of the present invention is to provide a laminated optical film whose characteristics are not impaired by a bonding method using an ultraviolet-curable adhesive which is excellent in workability and efficiency in mass production.
前記本発明の目的は、担体光学部材面に高屈折率層と
低屈折率層とを積層、担持させ、該形成された積層膜を
差挟んで、紫外線硬化型接着剤で接合光学部材面を接合
した光学素子において、少くとも前記接合光学部材面に
最も近い前記高屈折率層が酸化プラセオジムと酸化チタ
ニウムとを含有し、混成されていることを特徴とする光
学素子によって達成される。The object of the present invention is to stack and support a high refractive index layer and a low refractive index layer on the carrier optical member surface, sandwich the formed laminated film, and bond the optical member surface with an ultraviolet curable adhesive. In the bonded optical element, at least the high refractive index layer closest to the surface of the bonded optical member contains praseodymium oxide and titanium oxide and is hybridized.
尚本発明の態様としては前記混成高屈折率層に組合せ
る低屈折率層の形成には酸化珪素、代表的にはSiO2、ま
たは弗化マグネシウム、代表的にはMgF2を用いることが
好ましい。As an embodiment of the present invention, it is preferable to use silicon oxide, typically SiO 2 , or magnesium fluoride, typically MgF 2 for forming the low refractive index layer combined with the hybrid high refractive index layer. .
また積層数は必要に応じ任意に定めうるが、本発明に
おいては接合光学部材面に最も近い高屈折率層が前記混
成高屈折率層であれば充分であるがすべての高屈折率層
が混成高屈折率層であることが好ましい。また該混成層
においてプラセオジウム/チタニウムの比は0.5〜5、
好ましくは2〜3である。The number of layers can be arbitrarily determined as necessary. In the present invention, it is sufficient if the high refractive index layer closest to the surface of the joined optical member is the hybrid high refractive index layer, but all the high refractive index layers are hybrid. It is preferably a high refractive index layer. The ratio of praseodymium / titanium in the hybrid layer is 0.5-5,
Preferably it is 2-3.
更にZr,Ta,Y,La等の金属及び/又はそれらの酸化物が
特性を損わぬ範囲含有されていてもよい。Further, metals such as Zr, Ta, Y, La and / or oxides thereof may be contained in a range that does not impair the properties.
尚接着剤の層のみを介して接合光学部材面に直面する
積層光学膜の層は積層数に応じ高屈折率層であっても低
屈折率層であつても差支えない。The layer of the laminated optical film facing the surface of the joined optical member via only the adhesive layer may be a high refractive index layer or a low refractive index layer depending on the number of layers.
また積層光学膜の形成には各種の気相堆積法、例えば
真空蒸着、スパッタリング、イオンビーム蒸着等の物理
蒸着法或は反応ガスを制御しながらのCVD法等が任意に
用いられる。For forming the laminated optical film, various vapor deposition methods, for example, a physical vapor deposition method such as vacuum vapor deposition, sputtering, or ion beam vapor deposition, or a CVD method while controlling a reaction gas, are arbitrarily used.
次に実施例によって本発明を具体的に説明する。 Next, the present invention will be specifically described with reference to examples.
実施例1 プラセオジウム酸化物とチタン酸化物とを主成分とす
る混合物(例えばE.Merck社製商品名“サブスタンス2";
以下、混合物)を高屈折率物質、SiO2を低屈折率物質と
して、担体ガラスプリズム(材質:BK7)上に真空蒸発を
用いて交互に23層積層した。蒸着時、基板加熱温度は35
0℃であった。蒸着開始真空度は1×10-5Torr、混合物
は蒸着速度4Å/sec、SiO2は10Å/secで蒸着を行ない、
蒸着中2×10-4Torrの真空度を保つよう真空槽内に酸素
ガスを導入した。Example 1 A mixture containing praseodymium oxide and titanium oxide as main components (for example, trade name "Substance 2" manufactured by E. Merck;
Hereinafter, 23 layers were alternately laminated on a carrier glass prism (material: BK7) by using vacuum evaporation, using the mixture as a high refractive index substance and SiO 2 as a low refractive index substance. During deposition, the substrate heating temperature is 35
It was 0 ° C. The vacuum at the start of deposition is 1 × 10 -5 Torr, the mixture is deposited at a deposition rate of 4 ° / sec, and SiO 2 is deposited at a rate of 10 ° / sec.
Oxygen gas was introduced into the vacuum chamber so as to maintain a vacuum of 2 × 10 −4 Torr during the vapor deposition.
蒸着後、プリズムを大気中に取出し、接合ガラスプリ
ズム(材質:BK7)と、紫外線硬化型接着剤(ノーランド
社製No.61)を用いて接合した。10mw/cm2の強さの紫外
線を仮固定に5秒間、本硬化に10分間照射し、第1図に
示す光学素子を作成した。After the vapor deposition, the prism was taken out into the atmosphere, and bonded to a bonded glass prism (material: BK7) using an ultraviolet-curable adhesive (No. 61 manufactured by Norland). Ultraviolet rays having an intensity of 10 mw / cm 2 were irradiated for 5 seconds for temporary fixing and 10 minutes for main curing to prepare an optical element shown in FIG.
仮固定後と、本硬化後に、このプリズムへ垂直に光を
入射させた時(積層膜への入射角は45゜)の分光透過率
を示す(第3図)。仮固定後と本硬化後とではまったく
差は認められなかった。The spectral transmittance is shown when light is vertically incident on the prism after the temporary fixing and after the main curing (the incident angle on the laminated film is 45 °) (FIG. 3). No difference was observed between after temporary fixing and after full curing.
なお積層膜の層構成は第1表の通りである。 The layer configuration of the laminated film is as shown in Table 1.
実施例2 実施例1と同じ物質を第2図の担体プリズム(材質:B
K7)上に積層し、紫外線硬化接着剤を用い接合プリズム
と接合し、透過率50%のカット波長が約650nmのロング
パスフィルタを作製した。蒸着条件、接合条件は実施例
1と同じで積層膜は29層からなる。Example 2 The same substance as in Example 1 was applied to the carrier prism shown in FIG. 2 (material: B
K7), and bonded with a bonding prism using an ultraviolet-curing adhesive to produce a long-pass filter with a transmittance of 50% and a cut wavelength of about 650 nm. The deposition conditions and bonding conditions were the same as in Example 1, and the laminated film was composed of 29 layers.
仮固定後と本硬化後に、積層膜に入射角30゜で光を入
射させ、分光透過率を測定したが、まったく差異は生じ
なかった。本硬化後の透過率曲線を第4図に示す。After the temporary fixing and the main curing, light was incident on the laminated film at an incident angle of 30 °, and the spectral transmittance was measured. As a result, no difference occurred. FIG. 4 shows the transmittance curve after the main curing.
なお、積層膜の層構成は第2表に示す通りである。 The layer configuration of the laminated film is as shown in Table 2.
実施例3 実施例2と同じ形状の担体プリズム上にTiO2とSiO2を
交互に26層蒸着し、さらにその上に混成層を1層蒸着し
た。Example 3 26 layers of TiO 2 and SiO 2 were alternately vapor-deposited on a carrier prism having the same shape as in Example 2, and a single layer of a hybrid layer was further vapor-deposited thereon.
TiO2は、3×10-4Torrの酸素ガス圧のもと、4Å/sec
の速度で蒸着した。その他は、上記実施例と同じ蒸着条
件であった。このプリズムと接合プリズムとを上記実施
例と同じ接合条件で接着し、ロングパスフィルタを作製
した。TiO 2 is 4Å / sec under oxygen gas pressure of 3 × 10 -4 Torr
Was deposited at the following speed. The other conditions were the same as those of the above-described embodiment. The prism and the cemented prism were adhered under the same joining conditions as in the above-described embodiment, to produce a long-pass filter.
実施例2と同一条件で仮固定後と、本硬化後にプリズ
ムの分光特性を調べたが差異は生じていなかった。The spectral characteristics of the prism after the temporary fixing under the same conditions as in Example 2 and after the main curing were examined, but no difference was found.
第5図に本硬化後の測定曲線を示す。 FIG. 5 shows a measurement curve after the main curing.
積層膜の構成は第3表に示す通りである。 The configuration of the laminated film is as shown in Table 3.
実施例4 実施例1と同一形状の担体プリズム上に、混成層とMg
F2層の交互積層膜を蒸着し、接合プリズムと接合するこ
とで、P波を約4:1に分割する偏光ビームスプリッタを
作製した。Example 4 A hybrid layer and Mg were formed on a carrier prism having the same shape as in Example 1.
Depositing alternate laminated film of F 2 layer, by bonding the bonding prisms, the P-wave of about 4: to produce a polarizing beam splitter for splitting one.
MgF2は、3×10-5Torr以下の真空度で、8Å/secの速
度で蒸着し、混合物は、上記実施例と同じ条件で蒸着
し、交互9層の積層をした。蒸着後、上記実施例と同じ
く接合し、その仮固定後、本硬化後にP波、S波の透過
率を測定したが劣化は認められなかった。第6図にその
測定曲線を示す。積層膜の構成は、第4表の通りであ
る。MgF 2 was deposited at a rate of 8 ° / sec at a vacuum degree of 3 × 10 −5 Torr or less, and the mixture was deposited under the same conditions as in the above example, and nine alternate layers were laminated. After vapor deposition, bonding was performed in the same manner as in the above example, and after temporary fixing, and after main curing, the transmittance of P-waves and S-waves was measured. FIG. 6 shows the measurement curve. Table 4 shows the configuration of the laminated film.
尚MgF2蒸着中にArなどの不活性ガスを蒸着装置中に導
入することにより、膜厚の均一化が図れる。また弗素系
のガス(例えばCF4)を導入すれば膜厚の均一化と共に
膜質の向上が図れる。Note that the film thickness can be made uniform by introducing an inert gas such as Ar into the vapor deposition apparatus during the MgF 2 vapor deposition. If a fluorine-based gas (for example, CF 4 ) is introduced, the film thickness can be made uniform and the film quality can be improved.
〔発明の効果〕 以上、第7図に示した従来のものに比べ本発明に係る
混成層を用いることにより、紫外線硬化接着剤を用いて
も特性の劣化しない光学素子が実現できることがわかっ
た。 [Effects of the Invention] As described above, it has been found that the use of the hybrid layer according to the present invention as compared with the conventional one shown in FIG. 7 enables the realization of an optical element whose characteristics are not deteriorated even when an ultraviolet curing adhesive is used.
第1図は実施例1及び4の光学素子の形態、第2図は実
施例及び3の光学素子の形態を示す。第3図及び第6図
はTp及びTsの透過率を示すグラフであり、また第4図及
び第5図は白色光の透過スペクトルである。 1……担体プリズム 2……積層光学膜 3……紫外線硬化型接着剤層 4……接合プリズム L……入射光FIG. 1 shows the forms of the optical elements of Examples 1 and 4, and FIG. 2 shows the forms of the optical elements of Examples and 3. 3 and 6 are graphs showing the transmittance of Tp and Ts, and FIGS. 4 and 5 are the transmission spectra of white light. DESCRIPTION OF SYMBOLS 1 ... Carrier prism 2 ... Laminated optical film 3 ... Ultraviolet curable adhesive layer 4 ... Junction prism L ... Incident light
Claims (2)
とを積層、担持させ、該形成された積層膜を差挟んで、
紫外線硬化型接着剤で接合光学部材面を接合した光学素
子において、少くとも前記接合光学部材面に最も近い前
記高屈折率層が酸化プラセオジムと酸化チタニウムとを
含有し、混成されていることを特徴とする光学素子。1. A high-refractive-index layer and a low-refractive-index layer are laminated and supported on the surface of a carrier optical member, and the formed laminated film is sandwiched therebetween.
In the optical element in which the joining optical member surfaces are joined by an ultraviolet curing adhesive, at least the high refractive index layer closest to the joining optical member surface contains praseodymium oxide and titanium oxide, and is mixed. Optical element.
シウムから形成されていることを特徴とする請求項1に
記載の光学素子。2. The optical element according to claim 1, wherein said low refractive index layer is formed of silicon oxide or magnesium fluoride.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1117119A JP2717702B2 (en) | 1989-05-09 | 1989-05-09 | Optical element |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1117119A JP2717702B2 (en) | 1989-05-09 | 1989-05-09 | Optical element |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02294601A JPH02294601A (en) | 1990-12-05 |
| JP2717702B2 true JP2717702B2 (en) | 1998-02-25 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1117119A Expired - Fee Related JP2717702B2 (en) | 1989-05-09 | 1989-05-09 | Optical element |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2717702B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2881498B2 (en) | 1990-11-30 | 1999-04-12 | コニカ株式会社 | Multilayer thin film optical element |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006195301A (en) * | 2005-01-17 | 2006-07-27 | Konica Minolta Opto Inc | Optical element |
-
1989
- 1989-05-09 JP JP1117119A patent/JP2717702B2/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2881498B2 (en) | 1990-11-30 | 1999-04-12 | コニカ株式会社 | Multilayer thin film optical element |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02294601A (en) | 1990-12-05 |
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