JPH035341A - Optical glass - Google Patents
Optical glassInfo
- Publication number
- JPH035341A JPH035341A JP13809289A JP13809289A JPH035341A JP H035341 A JPH035341 A JP H035341A JP 13809289 A JP13809289 A JP 13809289A JP 13809289 A JP13809289 A JP 13809289A JP H035341 A JPH035341 A JP H035341A
- Authority
- JP
- Japan
- Prior art keywords
- glass
- optical
- optical glass
- amount
- chemical durability
- 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
- 239000005304 optical glass Substances 0.000 title claims abstract description 20
- 239000000203 mixture Substances 0.000 claims description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 12
- 239000000126 substance Substances 0.000 abstract description 12
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract description 8
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 abstract description 8
- MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum oxide Inorganic materials [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 abstract description 7
- 239000000377 silicon dioxide Substances 0.000 abstract description 6
- 229910052681 coesite Inorganic materials 0.000 abstract 3
- 229910052906 cristobalite Inorganic materials 0.000 abstract 3
- KTUFCUMIWABKDW-UHFFFAOYSA-N oxo(oxolanthaniooxy)lanthanum Chemical compound O=[La]O[La]=O KTUFCUMIWABKDW-UHFFFAOYSA-N 0.000 abstract 3
- 235000012239 silicon dioxide Nutrition 0.000 abstract 3
- 229910052682 stishovite Inorganic materials 0.000 abstract 3
- 229910052905 tridymite Inorganic materials 0.000 abstract 3
- FUJCRWPEOMXPAD-UHFFFAOYSA-N Li2O Inorganic materials [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 abstract 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 2
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Inorganic materials [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 abstract 2
- 229910052593 corundum Inorganic materials 0.000 abstract 2
- XUCJHNOBJLKZNU-UHFFFAOYSA-M dilithium;hydroxide Chemical compound [Li+].[Li+].[OH-] XUCJHNOBJLKZNU-UHFFFAOYSA-M 0.000 abstract 2
- 229910001845 yogo sapphire Inorganic materials 0.000 abstract 2
- 229910018404 Al2 O3 Inorganic materials 0.000 abstract 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 abstract 1
- 238000002156 mixing Methods 0.000 abstract 1
- 239000011521 glass Substances 0.000 description 25
- 230000003287 optical effect Effects 0.000 description 16
- 239000005331 crown glasses (windows) Substances 0.000 description 10
- 238000002844 melting Methods 0.000 description 10
- 230000008018 melting Effects 0.000 description 10
- 238000000465 moulding Methods 0.000 description 9
- 229910052788 barium Inorganic materials 0.000 description 7
- 230000007423 decrease Effects 0.000 description 7
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 6
- 238000004031 devitrification Methods 0.000 description 5
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- DHEQXMRUPNDRPG-UHFFFAOYSA-N strontium nitrate Chemical compound [Sr+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O DHEQXMRUPNDRPG-UHFFFAOYSA-N 0.000 description 4
- 239000011787 zinc oxide Substances 0.000 description 4
- 235000014692 zinc oxide Nutrition 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000006063 cullet Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 2
- 229910052808 lithium carbonate Inorganic materials 0.000 description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 2
- 239000001095 magnesium carbonate Substances 0.000 description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 2
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Inorganic materials [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- 229910001928 zirconium oxide Inorganic materials 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241000872931 Myoporum sandwicense Species 0.000 description 1
- 235000010575 Pueraria lobata Nutrition 0.000 description 1
- 241000219781 Pueraria montana var. lobata Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- -1 etc. are used Substances 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000000156 glass melt Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- BDAGIHXWWSANSR-NJFSPNSNSA-N hydroxyformaldehyde Chemical compound O[14CH]=O BDAGIHXWWSANSR-NJFSPNSNSA-N 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 231100000989 no adverse effect Toxicity 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 238000007517 polishing process Methods 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 229910000018 strontium carbonate Inorganic materials 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/062—Glass compositions containing silica with less than 40% silica by weight
- C03C3/064—Glass compositions containing silica with less than 40% silica by weight containing boron
- C03C3/068—Glass compositions containing silica with less than 40% silica by weight containing boron containing rare earths
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)
- Glass Compositions (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、屈折率(nd )が1.58〜なる組成を有
し、屈折率(nd)が50〜62である光学ガラスに係
り、特に、上記光学恒数を有し、バリウムクラウンガラ
スおよび重クラウンガラスとして分類される光学ガラス
に関する。Detailed Description of the Invention [Industrial Application Field] The present invention relates to an optical glass having a composition having a refractive index (nd) of 1.58 to 50 and a refractive index (nd) of 50 to 62. In particular, it relates to optical glasses having the above optical constants and classified as barium crown glasses and heavy crown glasses.
[従来の技術]
nd 1. 58〜1. 67、シd50〜62なる光
学恒数を有し、バリウムクラウンガラスあるいは重クラ
ウンガラスとして分類される光学ガラスは、古くから大
量に生産されてきている。[Prior art] nd 1. 58-1. Optical glasses having optical constants of 67 and d50 to 62 and classified as barium crown glass or heavy crown glass have been produced in large quantities for a long time.
[発明が解決しようとする課題]
近年、光学ガラスを製造するにあたり、ガス燃焼により
ガラスを熔かす従来法よりも熱効率に優れ、公害の発生
も少ない直接通電熔融が広く行われてきている。この直
接通電熔融は、ガラス融液の電気抵抗によるジュール熱
を利用してガラスを熔かすものである。[Problems to be Solved by the Invention] In recent years, direct current melting has been widely used in the production of optical glass, as it has superior thermal efficiency and generates less pollution than the conventional method of melting glass by gas combustion. This direct current melting uses Joule heat due to the electrical resistance of the glass melt to melt the glass.
しかしながら、nd 1.58〜1.67、シd50
〜62なる光学恒数を有し、バリウムクラウンガラスあ
るいは重クラウンガラスとして分類されるガラスは、電
気抵抗値が大きすぎるため、直接通電熔融が極めて困難
であるという問題があった。However, nd 1.58-1.67, d50
Glass that has an optical constant of ~62 and is classified as barium crown glass or heavy crown glass has a problem in that it is extremely difficult to directly melt it with electricity because its electrical resistance value is too large.
また、光学ガラス成形品を得るにあたっては、研摩工程
を必要とせず、プレス加工のみで最終レンズ製品を得る
、いわゆるモールド成形が、近年、脚光を浴びている。Furthermore, in order to obtain optical glass molded products, so-called molding, which does not require a polishing process and obtains the final lens product only by pressing, has been attracting attention in recent years.
しかしながら、バリウムクラウンガラスあるいは重クラ
ウンガラスとして分類されるガラスにモールド成形を適
用した場合、これらのガラスは屈伏点が高いために成形
温度の上昇をまねき、成形精度の低下、金型の劣化等を
引き起こす。このため、モールド成形にはガラスの屈伏
点をできるだけ低くすることが望ましいが、一般に、ガ
ラスの屈伏点を低くしようとすると、ガラスの化学的耐
久性が低下するのが通例であり、モールド成形に適し、
化学的耐久性にも優れたバリウムクラウンガラスあるい
は重クラウンガラスを得ることは困難であった。However, when molding is applied to glass classified as barium crown glass or heavy crown glass, the high yielding point of these glasses causes an increase in molding temperature, resulting in a decrease in molding accuracy and deterioration of the mold. cause. For this reason, it is desirable to lower the deformation point of glass as much as possible for mold forming, but in general, when trying to lower the deformation point of glass, the chemical durability of the glass usually decreases, so mold forming suitable,
It has been difficult to obtain barium crown glass or heavy crown glass that also has excellent chemical durability.
したがって本発明の目的は、nd 1.58〜1゜67
、シd50〜62なる光学恒数を有し、直接通電熔融に
適した低い電気抵抗値を持ち、モールド成形に適する低
い屈伏点を持つとともに、優れた化学的耐久性を有する
光学ガラスを提供することにある。Therefore, the object of the present invention is to
, an optical constant of 50 to 62, a low electrical resistance suitable for direct current melting, a low yield point suitable for mold forming, and excellent chemical durability. There is a particular thing.
[課題を解決するための手段]
本発明は、上記目的を解決するためになされたもので、
本発明の光学ガラスは、
SiO+ +B+Ox 36〜62w
t%(ただし、SiO+ 23〜62wt%B
I03 0〜28wt%)
Li+0 0. 5〜7wt%Ba
O12〜52wt%
La+Ox +Al103 +2rO++TiO+
1〜18wt%(ただし、La+Ot 0. 5
〜11wt%Al20xO〜 7vt%
Zto+ 0〜8vt%
Ti1t O〜2wt%)NaIo
0〜5wt%に20
0〜5wt%MgO0〜10wt%
CaOO〜15vt%
SrOO〜20vt%
Z口0
0〜14wt%なる組成を有し、屈折率(n
d )が1.58〜1゜67でアツベ数(νd)が50
〜62であることを特徴とするものである。[Means for Solving the Problems] The present invention has been made to solve the above objects, and
The optical glass of the present invention has SiO+ +B+Ox 36~62w
t% (However, SiO+ 23-62wt%B
I03 0-28wt%) Li+0 0. 5-7wt%Ba
O12~52wt% La+Ox +Al103 +2rO++TiO+
1 to 18 wt% (However, La + Ot 0.5
~11wt%Al20xO~ 7vt% Zto+ 0~8vt% Ti1t O~2wt%) NaIo
20 to 0-5wt%
0~5wt%MgO0~10wt% CaOO~15vt% SrOO~20vt% Z port 0
It has a composition of 0 to 14 wt%, and a refractive index (n
d) is 1.58 to 1°67 and the Atsbe number (νd) is 50.
~62.
ガラスの組成を上記のように厳密に限定することにより
、本発明の目的である、nd 1.58〜1.67、シ
d50〜62なる光学恒数を有し、直接通電熔融に適し
た低い電気抵抗値を持ち、モールド成形に適する低い屈
伏点を持つとともに、優れた化学的耐久性を有する光学
ガラスを提供することが可能となる。By strictly limiting the composition of the glass as described above, it has optical constants of nd 1.58 to 1.67 and sid 50 to 62, which are the objects of the present invention, and has low optical constants suitable for direct current melting. It becomes possible to provide optical glass that has an electrical resistance value, a low yield point suitable for molding, and excellent chemical durability.
各成分の限定理由は以下のとうりである。The reasons for limiting each component are as follows.
SiO+とBl 03とはガラス骨格を作る成分であり
、合計量が36vt%未満ではndが高くなり過ぎるた
め36wt%以上必要であるが、62wt%を超えると
ndが逆に低くなりすぎるため、これらの成分の合計量
は36〜62wt%に限定される。そして、化学的耐久
性に優れたガラスを得るためには、23wt%以上の5
iQ1が必要であり、28wt%を超えてB2O3を含
有させてはならない。したがって、Sighの量は23
〜62wt%に、またB+ Osの量は0〜28wt%
に、それぞれ限定される。SiO+ and Bl 03 are components that form the glass skeleton, and if the total amount is less than 36 wt%, nd will be too high, so 36 wt% or more is required, but if it exceeds 62 wt%, nd will be too low, so these The total amount of the components is limited to 36-62 wt%. In order to obtain glass with excellent chemical durability, it is necessary to
iQ1 is required, and B2O3 must not be contained in an amount exceeding 28 wt%. Therefore, the amount of Sigh is 23
~62wt%, and the amount of B+ Os is 0~28wt%
Each is limited to
Li1Oはガラスの電気抵抗値と屈伏点を下げるのに効
果的な成分であり、0. 5wt%以上必要であるが、
7wt%を超えるとガラスの化学的耐久性が低下すると
ともに耐失透性が低下するため、Lil Qの量は0.
5〜7wt%に限定される。Li1O is an effective component for lowering the electrical resistance value and yielding point of glass; Although 5wt% or more is required,
If the amount exceeds 7 wt%, the chemical durability of the glass and devitrification resistance will decrease, so the amount of Lil Q should be 0.
It is limited to 5 to 7 wt%.
BaOは所望のndとνdを得るのに必須の成分であり
、12wt%以上必要であるが、52wt%を超えると
ガラスの化学的耐久性が低下するため、BaOの量は1
2〜52wt%に限定される。BaO is an essential component to obtain the desired nd and νd, and is required in an amount of 12 wt% or more, but if it exceeds 52 wt%, the chemical durability of the glass will decrease, so the amount of BaO should be 1.
It is limited to 2 to 52 wt%.
La+Ox 、AI+03.1rorおよびTiO+は
、ガラスの化学的耐久性を改善する成分であるとともに
耐失透性の改善に有効な成分であり、合計量で1wt%
以上必要である。中でもLa+03 はその効果が顕著
であり、熔融性等へ悪影響を及さないばかりでなく高屈
折率、低分散のガラスを得るのに有利である等、利点が
多いので、Q、 5wt%以上必要である。しかしな
がら、La+Osは原料が比較的高価であるため、11
wt%を超えて含有させるのは得策でない。AlIO3
の量が7wt%を超えるとガラスの耐失透性が低下し、
1rorの量が8vt%を超えた場合も同様である。ま
た、Ti11の量が2wt%を超えるとガラスの透過率
が低下する。これらの理由により、1a103の量は0
.5〜1lvt%に、AI+O葛の量はQ 〜7 wt
%に、Zr0Iの量は0〜8wt%に、TiO+の量は
0〜2wt%にそれぞれ限定され、これらの成分の合計
量は1〜18wt%に限定される。La+Ox, AI+03.1ror, and TiO+ are components that improve the chemical durability of glass as well as effective components for improving devitrification resistance, and the total amount is 1wt%.
The above is necessary. Among them, La+03 has a remarkable effect and has many advantages such as not only having no adverse effect on melting properties but also being advantageous for obtaining glass with high refractive index and low dispersion, so Q: 5wt% or more is required. It is. However, since the raw materials for La+Os are relatively expensive, 11
It is not a good idea to contain more than wt%. AlIO3
When the amount exceeds 7 wt%, the devitrification resistance of the glass decreases,
The same applies when the amount of 1ror exceeds 8vt%. Furthermore, when the amount of Ti11 exceeds 2 wt%, the transmittance of the glass decreases. For these reasons, the amount of 1a103 is 0
.. 5-1 lvt%, the amount of AI + O kudzu is Q ~ 7 wt
%, the amount of Zr0I is limited to 0-8 wt%, the amount of TiO+ is limited to 0-2 wt%, and the total amount of these components is limited to 1-18 wt%.
Na+ 01K10 、MgO、CaO、SrOおよび
200は、光学恒数の調整、耐失透性の改善、熔融性の
改善等の目的で、夫々0〜5wt%、O〜5vt%、0
〜1Qvt%、0〜15vt%、0〜20wt%および
0〜14wt%の範囲で含有させることができるが、夫
々の範囲を超えると、化学的耐久性の低下や耐失透性の
低下をまねくため、これらの成分の量は上記範囲に限定
される。Na+ 01K10, MgO, CaO, SrO and 200 are used in amounts of 0 to 5 wt%, O to 5 vt%, and 0, respectively, for the purpose of adjusting optical constants, improving devitrification resistance, improving meltability, etc.
It can be contained in the ranges of ~1Qvt%, 0-15vt%, 0-20wt%, and 0-14wt%, but exceeding each range will lead to a decrease in chemical durability and devitrification resistance. Therefore, the amounts of these components are limited to the above ranges.
なお本発明の光学ガラスにおいては、上述した成分の他
に、通常使用されるAS+03 、Sb+03等の脱泡
剤や、ガラスの特性を悪化させない範囲での少量のF
5PI05SPbO等を添加することもできる。In addition to the above-mentioned components, the optical glass of the present invention also contains commonly used defoaming agents such as AS+03 and Sb+03, and a small amount of F within a range that does not deteriorate the properties of the glass.
5PI05SPbO etc. can also be added.
本発明の光学ガラスは、原料として通常使用される硅石
粉、硼酸、炭酸リチウム、炭酸バリウム、酸化ランタン
、水酸化アルミニウム、酸化ジルコニウム、酸化チタン
、炭酸ナトリウム、硝酸ナトリウム、炭酸カリウム、硝
酸カリウム、水酸化マグネシウム、炭酸マグネシウム、
炭酸カルシウム、硝酸ストロンチウム、炭酸ストロンチ
ウム、酸化亜鉛(亜鉛華)等を用い、これらの原料から
なる混合物を白金製坩堝等の耐熱性容器に入れて120
0〜1400℃に加熱して熔解させ、撹拌して均質化、
泡切れを行った後、適当な温度に予熱した金型に鋳込み
徐冷することにより得ることができる。The optical glass of the present invention is made of silica powder, boric acid, lithium carbonate, barium carbonate, lanthanum oxide, aluminum hydroxide, zirconium oxide, titanium oxide, sodium carbonate, sodium nitrate, potassium carbonate, potassium nitrate, and hydroxide, which are commonly used as raw materials. magnesium, magnesium carbonate,
Calcium carbonate, strontium nitrate, strontium carbonate, zinc oxide (zinc white), etc. are used, and a mixture of these raw materials is placed in a heat-resistant container such as a platinum crucible for 120 minutes.
Heat to 0-1400℃ to melt, stir and homogenize,
After removing the bubbles, it can be obtained by pouring into a mold preheated to an appropriate temperature and slowly cooling.
このときのガラスの熔融は、直接通電熔融も含めた従来
手法をそのまま適用することができ、成形加工も、モー
ルド成形を含む従来手法をそのまま適用することができ
る。For melting the glass at this time, conventional methods including direct current melting can be directly applied, and for molding, conventional methods including molding can be applied as is.
[実施例] 以下、本発明の実施例について説明する。[Example] Examples of the present invention will be described below.
実施例1〜4
実施例1〜4の光学ガラスの出発原料として、硅石粉、
硼酸、炭酸リチウム、炭酸バリウム、酸化ランタン、水
酸化アルミニウム、酸化ジルコニウム、酸化チタン、炭
酸ナトリウム、炭酸カリウム、炭酸マグネシウム、炭酸
カルシウム、硝酸ストロンチウムおよび酸化亜鉛(亜鉛
華)を用い、これらの出発原料を、最終的に得られるガ
ラスの組成が表−1に示す組成となるように実施例毎に
秤量して、瑞瑞乳鉢で十分に混合した後、得られた混合
物をシリカ坩堝で粗熔解させ、実施例毎にカレットを得
た。Examples 1 to 4 As starting materials for the optical glasses of Examples 1 to 4, silica powder,
Using boric acid, lithium carbonate, barium carbonate, lanthanum oxide, aluminum hydroxide, zirconium oxide, titanium oxide, sodium carbonate, potassium carbonate, magnesium carbonate, calcium carbonate, strontium nitrate, and zinc oxide (zinc white), these starting materials are Weighed each example so that the composition of the final glass would be as shown in Table 1, mixed thoroughly in a Zuizui mortar, and then coarsely melted the resulting mixture in a silica crucible. Cullet was obtained for each example.
次いで、得られたカレットを、ジルコニア系電鋳レンガ
で作られた溶融炉に入れ、直接通電熔融により1250
〜1300℃に加熱して熔融させ、撹拌して均質化を図
り、泡切れを行った後、金型を用いて板状に成形し、徐
冷して板状の光学ガラスを得た。次に板状ガラスから所
定重量のガラス塊を切出し、従来の研摩法により球状プ
リフォームを得た後、モールド成形により計4種類の非
球面凸レンズ状の光学レンズを得た。Next, the obtained cullet was placed in a melting furnace made of zirconia electroformed bricks and melted by direct electric current to a temperature of 1250
After heating to ~1300°C to melt, stirring to homogenize, and removing bubbles, it was molded into a plate using a mold, and slowly cooled to obtain a plate-shaped optical glass. Next, a glass gob of a predetermined weight was cut out from the plate glass, a spherical preform was obtained by a conventional polishing method, and a total of four types of aspherical convex optical lenses were obtained by molding.
このようにして得られた各光学レンズの、ヘリウムラン
プのd線に対する屈折率(nd ) 、アツベ数(νd
)および屈伏点を測定したところ、ndが1.589〜
1.658、νdが51〜61、屈伏点が570〜59
5℃であり、いずれの実施例で得られた光学レンズも、
所望のnd及びνdを有するとともに、モールド成形に
適する低い屈伏点を持つことが確認された。The refractive index (nd) and Atsube number (νd) of each optical lens obtained in this way with respect to the d-line of the helium lamp are
) and yield point were measured, nd was 1.589 ~
1.658, νd is 51-61, yield point is 570-59
5°C, and the optical lenses obtained in any of the examples also had
It was confirmed that it had the desired nd and vd as well as a low yielding point suitable for molding.
また、各実施例で得られた光学レンズの耐酸性(Da)
および耐水性(Dw )を、それぞれJOGIS(日本
光学硝子工業会規格)06 1975に基づいて測定し
たところ、Daが0.18〜0゜70wt%(ただし、
減量率) 、Dwが0.01〜0.06wt%(ただし
、減量率)であり、いずれの光学レンズも化学的耐久性
に優れていることが確認された。In addition, the acid resistance (Da) of the optical lens obtained in each example
and water resistance (Dw) were measured based on JOGIS (Japan Optical Glass Industry Association Standards) 06 1975.
Weight loss rate) and Dw were 0.01 to 0.06 wt% (however, weight loss rate), and it was confirmed that all optical lenses had excellent chemical durability.
さらに、実施例1〜2で得られた光学レンズの比抵抗を
測定したところ、第1図に示すように、従来のバリウム
クラウンガラスおよび重クラウンガラスに比べて、はる
かに低い電気抵抗値を持つことが確認された。Furthermore, when we measured the specific resistance of the optical lenses obtained in Examples 1 and 2, we found that they had a much lower electrical resistance value than conventional barium crown glass and heavy crown glass, as shown in Figure 1. This was confirmed.
比較例1〜2
従来の重クラウンガラスであるSK5と5SK5の組成
、nd 、νd 、屈伏点、DaおよびDWを表−1の
比較例1と比較例2にそれぞれ示す。Comparative Examples 1 and 2 The compositions, nd, vd, deformation points, Da, and DW of SK5 and 5SK5, which are conventional heavy crown glasses, are shown in Comparative Examples 1 and 2 in Table 1, respectively.
表−1から明らかなように、SK5のnd、νdは実施
例1と同一であるが、屈伏点が実施例1よりも100℃
以上も高い。また、5SK5のnd、νdは実施例2と
同一であるが、屈伏点が実施例2よりも100℃近くも
高い。As is clear from Table 1, nd and νd of SK5 are the same as those of Example 1, but the yield point is 100°C higher than that of Example 1.
Even more expensive. Furthermore, although nd and vd of 5SK5 are the same as those of Example 2, the yield point is nearly 100° C. higher than that of Example 2.
さらに、SK5および5SK5の比抵抗を測定したとこ
ろ、第1図に示すように、実施例1〜2で得られた光学
レンズに比べて、はるかに高い電気抵抗値を持つことが
確認された。Furthermore, when the specific resistance of SK5 and 5SK5 was measured, it was confirmed that they had much higher electrical resistance values than the optical lenses obtained in Examples 1 and 2, as shown in FIG.
(以下、余白)
[発明の効果コ
以上説明したように、本発明の光学ガラスは、nd 1
.58〜1.67、シd50〜62なる光学恒数を有し
、直接通電熔融に適した低い電気抵抗値を持ち、モール
ド成形に適する低い屈伏点を持つとともに、優れた化学
的耐久性を有している。(Hereinafter, blank space) [Effects of the invention As explained above, the optical glass of the present invention has nd 1
.. It has an optical constant of 58 to 1.67 and a sid of 50 to 62, a low electrical resistance value suitable for direct current melting, a low yield point suitable for mold forming, and excellent chemical durability. are doing.
したがって本発明を実施することにより、ndl、58
〜1.67、シd50〜62なる光学恒数を有する光学
ガラスの、製造工程の簡略化、生産コストの低減、納期
の短縮等を図ることが可能となる。Therefore, by practicing the present invention, ndl, 58
It becomes possible to simplify the manufacturing process, reduce production costs, shorten delivery time, etc. of optical glass having optical constants of ~1.67 and Sid50-62.
第1図は、実施例1.2の光学ガラスおよび比較例1.
2の光学ガラスの比抵抗と温度との関係を表すグラフで
ある。FIG. 1 shows the optical glass of Example 1.2 and Comparative Example 1.
2 is a graph showing the relationship between specific resistance and temperature of optical glass No. 2.
Claims (1)
ただし、SiO_2 23〜62wt% B_2O_3 0〜28wt%) Li_2O 0.5〜7wt% BaO 12〜52wt% Li_2O_3+Al_2O_3+ZrO_2+TiO
_2 1〜18wt%(ただし、La_2O_3 0.
5〜11wt%Al_2O_3 0〜7wt% ZrO_2 0〜8wt% TiO_2 0〜2wt%) Na_2O 0〜5wt% K_2O 0〜5wt% MgO 0〜10wt% CaO 0〜15wt% SrO 0〜20wt% ZnO 0〜14wt% なる組成を有し、屈折率(nd)が1.58〜1.67
でアッベ数(νd)が50〜62であることを特徴とす
る光学ガラス。(1) SiO_2+B_2O_3 36-62wt% (
However, SiO_2 23-62wt% B_2O_3 0-28wt%) Li_2O 0.5-7wt% BaO 12-52wt% Li_2O_3+Al_2O_3+ZrO_2+TiO
_2 1 to 18 wt% (However, La_2O_3 0.
5-11wt% Al_2O_3 0-7wt% ZrO_2 0-8wt% TiO_2 0-2wt%) Na_2O 0-5wt% K_2O 0-5wt% MgO 0-10wt% CaO 0-15wt% SrO 0-20wt% ZnO 0-1 4wt% It has a composition with a refractive index (nd) of 1.58 to 1.67.
An optical glass having an Abbe number (νd) of 50 to 62.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1138092A JP2535407B2 (en) | 1989-05-31 | 1989-05-31 | Optical glass |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1138092A JP2535407B2 (en) | 1989-05-31 | 1989-05-31 | Optical glass |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH035341A true JPH035341A (en) | 1991-01-11 |
JP2535407B2 JP2535407B2 (en) | 1996-09-18 |
Family
ID=15213766
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
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JPH0337130A (en) * | 1989-07-04 | 1991-02-18 | Sumita Kogaku Glass:Kk | Optical glass for precise press molding |
JPH06107426A (en) * | 1992-09-25 | 1994-04-19 | Ohara Inc | Optical glass |
JPH06107424A (en) * | 1992-09-25 | 1994-04-19 | Ohara Inc | Optical glass |
DE19703391C1 (en) * | 1997-01-30 | 1998-02-26 | Schott Glaswerke | A lead-free optical crown glass |
DE19738428C1 (en) * | 1997-09-03 | 1998-08-20 | Schott Glaswerke | New lead-free barium flint glass |
DE19733580A1 (en) * | 1997-08-02 | 1999-02-04 | Schott Glas | New lead-free optical heavy crown or double-heavy crown glass |
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JPS6046945A (en) * | 1983-08-22 | 1985-03-14 | Ohara Inc | Optical glass |
JPS62123040A (en) * | 1985-11-22 | 1987-06-04 | Sumita Kogaku Glass Seizosho:Kk | Optical glass |
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1989
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JPS58194755A (en) * | 1982-05-07 | 1983-11-12 | Ohara Inc | Optical glass |
JPS6046945A (en) * | 1983-08-22 | 1985-03-14 | Ohara Inc | Optical glass |
JPS62123040A (en) * | 1985-11-22 | 1987-06-04 | Sumita Kogaku Glass Seizosho:Kk | Optical glass |
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JPH0337130A (en) * | 1989-07-04 | 1991-02-18 | Sumita Kogaku Glass:Kk | Optical glass for precise press molding |
JPH06107426A (en) * | 1992-09-25 | 1994-04-19 | Ohara Inc | Optical glass |
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DE19733580A1 (en) * | 1997-08-02 | 1999-02-04 | Schott Glas | New lead-free optical heavy crown or double-heavy crown glass |
FR2766815A1 (en) * | 1997-08-02 | 1999-02-05 | Schott Glas | LEAD-FREE OPTICAL GLASSES, OF VERY HEAVY CROWN AND CROWN TYPE |
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