EP1472192A2 - Optisches glas - Google Patents

Optisches glas

Info

Publication number
EP1472192A2
EP1472192A2 EP03734594A EP03734594A EP1472192A2 EP 1472192 A2 EP1472192 A2 EP 1472192A2 EP 03734594 A EP03734594 A EP 03734594A EP 03734594 A EP03734594 A EP 03734594A EP 1472192 A2 EP1472192 A2 EP 1472192A2
Authority
EP
European Patent Office
Prior art keywords
weight
optical
glass
bao
zno
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.)
Withdrawn
Application number
EP03734594A
Other languages
German (de)
English (en)
French (fr)
Inventor
Silke Wolff
Ute Wölfel
Karl Mennemann
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.)
Schott AG
Original Assignee
Schott AG
Carl Zeiss AG
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 Schott AG, Carl Zeiss AG filed Critical Schott AG
Publication of EP1472192A2 publication Critical patent/EP1472192A2/de
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C3/00Glass compositions
    • C03C3/04Glass compositions containing silica
    • C03C3/062Glass compositions containing silica with less than 40% silica by weight
    • C03C3/07Glass compositions containing silica with less than 40% silica by weight containing lead

Definitions

  • the invention relates to an optical glass, in particular an optical glass for projection purposes with LCD projectors and the use thereof.
  • the market development in the projection sector continues to move towards larger projection areas.
  • the requirements placed on the projection devices with regard to the luminous efficacy and resolution of the projected image increase significantly.
  • the light yield determines the illumination of the irradiated area and the resolution the number of possible pixels. If the resolution is too low, the image appears grainy.
  • the centerpiece of a projection device is the modulation system, which impresses the light beam emanating from a light source with the desired image to be projected onto the projection surface.
  • the light beam is broken down into its basic colors (red, green, blue) and the desired modulation is impressed on each partial beam by means of an LCD (Liquid Crystal Display).
  • LCD Liquid Crystal Display
  • each of these cells is connected to a voltage source via a control unit in order to be able to assume the state “with voltage” or “without voltage” or “on” and “off”.
  • liquid crystals for modulating light beams: In one case, “On” means translucent and “Off” means opaque. This group forms the transmissive LCDs (tLCD) and is based on a transmissive beam path. In a second group, the incident light is reflected. In this group, “on” means that the plane of polarization of the incident and reflected light is rotated by ⁇ / 2. In the “off” state, the original polarization remains unchanged. This group forms the reflective LCDs (rLCD).
  • tLCD transmissive LCDs
  • rLCD reflective LCDs
  • the image is impressed on the three partial beams of a projection apparatus by rotating the plane of polarization instead of by blanking out the partial beams.
  • the incident light beam is first polarized using a polarizing filter and then divided into its basic colors by a beam splitter.
  • the properties "pole plane rotated” or “pole plane not rotated” are then imprinted.
  • the rays are also reflected.
  • the beams modulated in this way pass through the beam splitter in the opposite direction and are then used again. unite.
  • a downstream polar filter with the same direction finally filters out the untwisted portions of the three primary colors from the combined jet.
  • each cell also called pixel
  • the cell needs its own electronic control unit.
  • this control unit takes up a part of the cell area that can no longer be shone through by light, which reduces the light yield.
  • the light beam is reflected, so the control unit can be placed on the back of the cells without losing light.
  • the optical system of the rLCD devices is very sensitive to the slightest spatial deformation with a strong loss of contrast and color fringing. To explain this, the projection process for an rLCD system is explained in more detail:
  • the white light beam from a light source is polarized by an upstream polarizing filter and then falls on a polarizing beam splitter (PBS; Polarizing Beam Splitter), which reflects light whose polarization plane corresponds to that of the polarizing filter, and light that does so by ⁇ / 2, i.e. 90 ° is rotated.
  • PBS Polarizing Beam Splitter
  • the light polarized by the upstream polarizing filter is deflected 100% by reflection.
  • the beam then falls on the actual beam expensive, which, for. B. consists of four joined prisms, the inner parting surfaces of which are covered with steep color filter layers.
  • this beam splitter separates the white light beam into the partial beams for the three basic colors according to its wavelength.
  • a multitude of arrangements for beam splitters are known to the person skilled in the art which do not necessarily contain prisms.
  • the color beams emerging from the beam splitter fall on the rLCDs and illuminate them completely.
  • the light now finds the "on” and “off” pixels described above; accordingly, its plane of polarization is rotated or maintained. In any case, the light is reflected and runs the way back through the beam splitter to the PBS according to its wavelength. On the way back through the beam splitter, the three partial beams, which now contain the information about the overall image in the form of polarization state location information, are combined again.
  • the resulting white light beam is now separated in the PBS according to the polarization state of the wave trains. Trains with rotated plane of polarization are deflected by 90 ° like the incident beam, so they leave the projection beam path in the direction of the light source. Trains with a rotated polarization plane are let through directly and reach the projection surface, where they produce the desired image.
  • This so-called voltage-optical effect of rotating the plane of polarization of incident polarized light is caused in glass, for example, by insufficient fine cooling during manufacture. This freezes structural tensions in the glass, which result in different material and thus electron densities in the spatial directions. Since the refractive index of a material is defined by its electron density in the beam direction, the resulting refractive indexes differ in the different spatial directions. The material is optically anisotropic. If a linearly polarized wave train hits the material, its vectorial components are broken to different extents in the different spatial directions, which is equivalent to a rotation of the polarization plane.
  • the observed color fringes are also caused by the optical anisotropy.
  • the differently broken beam components are directed in different spatial directions, which leads to interference phenomena.
  • the difference in refractive index is wavelength-dependent, which gives the interference phenomena the colorful character of color fringes (stress birefringence).
  • projection devices are relatively small for reasons of manageability.
  • the optical components in these devices are exposed to large temperature differences and temperature changes of up to about 50 ° C, especially during commissioning, due to the spatial proximity to heat-emitting elements despite ventilation and the use of cooling elements. These temperature differences cause strong tensions in the glass.
  • the strength of the resulting optical effects is also dependent on the type of glass at the same voltage, since stresses have different effects due to the different glass structures.
  • the resulting stress birefringence and rotation of the polarization vector are therefore based on a material-specific quantity, the voltage-optical coefficient K.
  • a sensible glass optimization for use in projection can therefore only be the approximation of the voltage-optical coefficient to zero or the approximation of the photoelastic constants in the two directions.
  • the glass types known to date have an unacceptable relationship between the low K value and their chemical resistance and the Knoop hardness, since those components which, because of their high polarizability in the glass matrix (for example lead and phosphate), lower the K value, at the same time through this specific property Make the matrix particularly easy to influence and attack chemically and physically.
  • a low chemical resistance of a glass is not only relevant during its use. If this were the case, the problem could be solved, for example, with a protective coating.
  • a chemical resistance that is too low and, above all, a Knoop hardness that is too low are already noticeable during the cold post-processing of the optical components. Efflorescence, interference color effects and surface crystallization already occur during this cold post-processing, ie in a phase in which no protective lacquer and the like can be used. Too little Knoop hardness leads to enormous, difficult to control stock removal values in the standard machines used for cold finishing.
  • the object of the invention is therefore to provide an optical glass which, with sufficient chemical resistance and Knoop hardness, has such a small voltage-optical coefficient that it can be used in the field of projection, in particular for LCDs.
  • the invention is based on heavy flint glasses, such as those sold by Schott, Mainz, under the trade names SF 56, SF 57, SF 58 and SF 59. These are high-lead (often> 60% by weight, almost always> 50% by weight) lead silicate glasses with extremely low optional proportions of sodium, potassium and / or boron oxide (often> 5% by weight). They may contain small proportions of other elements for setting the refractive index, e.g. B. small proportions of titanium oxide (S. SF L 56). These types of glass are described, for example, in the Schott series "Properties of Optical Glass".
  • the optical glass according to the invention has the following composition (in% by weight on an oxide basis):
  • the total content of the alkali oxides of Na 2 0 and K 2 0 is preferably between 0.5 and 8% by weight and the sum of Ti0, Zr0 2 , La ⁇ 3, ZnO and BaO is between 1 and 7% by weight.
  • the lower limit of the sum of Ti0 2 , Zr0 2 , La 0 3 , ZnO and BaO 2 is in particular
  • the glasses according to the invention have a low stress-optical coefficient of -1.5 ⁇ K ⁇ 1.5, preferably -1 ⁇ K ⁇ 1 [10 ⁇ 6 mm 2 / N] and show good chemical resistance to alkaline agents (alkali resistance , AR) according to [ISO 10629] better or equal to class 3 or to acid (acid resistance, SR) according to ISO 8424 better or equal to class 53.
  • alkali resistance , AR alkali resistance
  • AR acid
  • SR acid resistance
  • the Knoop hardness is HK 0 , ⁇ ; 2 o ⁇ 300.
  • the glasses according to the invention are therefore well suited for all applications that benefit from low voltage-optical effects and that require good chemical resistance with a small voltage-optical coefficient, which in addition to the application area of projection, preferably LCD, in particular rLCD projection, also includes the areas of general imaging and telecommunications ,
  • the glasses according to the invention also meet the requirement for good meltability and machinability.
  • the glasses according to the invention can be doped with laser- or optoactive components, such as oxides of the elements Ga, Ge, Y, Nb, Mo, La, Ce, Pr, Nd, Gd, Tb, Dy, Ho, Er, Tn, Yb, Hf, Ta etc.
  • laser- or optoactive components such as oxides of the elements Ga, Ge, Y, Nb, Mo, La, Ce, Pr, Nd, Gd, Tb, Dy, Ho, Er, Tn, Yb, Hf, Ta etc.
  • the base glass on which the optical glass according to the invention is based comes from the lead silicate glass system common for heavy flint types with small, but essential for the invention, and thus mandatory proportions of titanium, zirconium, zinc, barium and / or lanthanum oxides.
  • the proportions of 5-35% by weight of SiO 2 and 55-88% by weight of PbO represent the glass formers of classic heavy flint types. They form the basis for the desired optical and physical properties of these types of glass, based on the additions of, according to the invention, mandatory Titanium, zirconium, zinc, barium and / or lanthanum oxide has been made to improve the chemical properties. A shift in the ratio of the glass formers to one another leads to negative effects in relation to the intended use.
  • boron trioxide can optionally be added at up to 10% by weight as a third glass former for stabilization against susceptibility to crystallization. It has also been found according to the invention that an additional addition has a very negative influence on the chemical resistance and the K value.
  • alkali metal oxides in particular 0-5% by weight Na 2 0 and or 0-5% by weight K0, it is possible on the one hand to fine-tune the optical position and on the other hand to reduce the susceptibility to crystallization, while in the present high-lead glasses, the properties as a flux are of minor importance.
  • a total content of 8% by weight should preferably not be exceeded, since in this case the K value may rises and the glasses can no longer be used as intended.
  • the lower limit of the total content of the alkali metal oxides Na 2 0 and K 0 is preferably 0.5% by weight.
  • variable addition of Ti0, Zr0 2 , La 2 0 3 , BaO and / or ZnO in the composition of its individual components serves to increase the chemical resistance and the knoop Hardness of the glasses according to the invention while maintaining low K values that correspond to the intended use.
  • the content of these components can easily be 0.
  • the lower limit is 1% by weight. It was also found that an addition exceeding the sum of 15% by weight, on the other hand, greatly reduces the crystallization stability.
  • Tables 1-4 contain 23 exemplary embodiments in the preferred composition range. These are comparative examples of the improved chemical resistance in relation to the low voltage-optical coefficient obtained. For this purpose, selected examples of the optical glass according to the invention were compared with known types with a corresponding voltage-optical coefficient.
  • the glass types sold by Schott, Mainz, under the trade names SF 56, SF 57, SF 58 and SF 59 serve as known types. These types of glass are described, for example, in the Schott "Properties of Optical Glass" series. The comparison is made on the basis of a composition that is as comparable as possible and not on the basis of an absolute reproduction of the optical position, since for the intended use a strict refractive index homogeneity of the individual pieces and a particularly good reproducibility of a defined optical position from batch to batch, but not the basic one Reinstallation of an optical position known from traditional optical glasses are relevant.
  • the glasses according to the invention are preferably free from arsenic. In order to keep the glass absolutely arsenic-free, it must not be refined with arsenic.
  • the glass is preferably free of aluminum or aluminum oxide.
  • fluorides can be used as refining agents which contain earth and alkali fluorides or other metals contained in the compositions as a counter ion, and antimony oxide and tin oxide, optionally also chlorides such as sodium chloride.
  • the invention also relates to a method for producing the glass according to the invention.
  • the glass-forming starting components known per se are heated as salts and / or oxides to form a melt, the 5-35% by weight SiO 2 55-88
  • the invention also relates to the use of the glass according to the invention in projectors, in particular rLCD projectors, in microlithography, telecommunications and in optical components, and to devices which contain glasses of this type.
  • Preferred projectors are LCD, in particular rLCD projectors.
  • Preferred optical components are optical laser glass and / or fiberglass, in particular for telecommunications.
  • a production example for the glasses according to the invention comprises the following:
  • the raw materials for the oxides preferably carbonates, nitrates and / or fluorides, are weighed out, one or more refining agents, such as Sb 2 0 3 , are added and then mixed well.
  • the glass batch is melted at approx. 1150 ° C in a continuous melting unit, then refined and homogenized at 1200 ° C.
  • the glass is hot processed, cooled in a defined manner and, if necessary, further processed to the desired dimensions.
  • the invention relates to optical glasses in the heavy flint and lanthanum heavy flint range which, due to their special optical, chemical and physical properties, are particularly suitable for use in application fields which benefit from low voltage-optical effects in their glass components (for example by utilizing polarization effects such as in the projection, refractive index homogeneity such as in microlithography or telecommunications) or through a coating compatibility in the optical sense (eg with special optical components).
  • the outstanding properties include, among other things, the zero stress-optical coefficient with good chemical resistance and sufficient Knoop hardness as well as good meltability and machinability.
  • the glasses according to the invention can also be used as optical laser glass or as telecommunications fiber glass with laser or optoactive components (for example: oxides of the elements Ga, Ge, Y, Nb, Mo, La, Ce, Pr, Nd, Gd, Tb, Dy, Ho, Er, Tn, Yb, Hf, Ta) can be doped.
  • laser or optoactive components for example: oxides of the elements Ga, Ge, Y, Nb, Mo, La, Ce, Pr, Nd, Gd, Tb, Dy, Ho, Er, Tn, Yb, Hf, Ta

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)
EP03734594A 2002-01-28 2003-01-28 Optisches glas Withdrawn EP1472192A2 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE10203226 2002-01-28
DE10203226A DE10203226A1 (de) 2002-01-28 2002-01-28 Optisches Glas
PCT/DE2003/000223 WO2003064340A2 (de) 2002-01-28 2003-01-28 Optisches glas

Publications (1)

Publication Number Publication Date
EP1472192A2 true EP1472192A2 (de) 2004-11-03

Family

ID=27634734

Family Applications (1)

Application Number Title Priority Date Filing Date
EP03734594A Withdrawn EP1472192A2 (de) 2002-01-28 2003-01-28 Optisches glas

Country Status (8)

Country Link
US (1) US20050075234A1 (ja)
EP (1) EP1472192A2 (ja)
JP (1) JP2005515954A (ja)
CN (1) CN1622922A (ja)
AU (1) AU2003210130A1 (ja)
DE (2) DE10203226A1 (ja)
RU (1) RU2004126253A (ja)
WO (1) WO2003064340A2 (ja)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8791631B2 (en) 2007-07-19 2014-07-29 Quarkstar Llc Light emitting device
WO2009012484A1 (en) * 2007-07-19 2009-01-22 University Of Cincinnati Nearly index-matched luminescent glass-phosphor composites for photonic applications
CZ2009373A3 (cs) * 2009-06-10 2010-10-13 Preciosa, A. S. Vysoceolovnaté sklo
DE102009027110B4 (de) * 2009-06-23 2012-02-16 Schott Ag Bleihaltiges Weltraumglas, seine Herstellung und Verwendung
DE102009027109B4 (de) * 2009-06-23 2012-02-16 Schott Ag Bleihaltiges Weltraumglas, seine Herstellung und Verwendung
WO2011052336A1 (ja) * 2009-10-29 2011-05-05 日本山村硝子株式会社 ガラス組成物及びそれを用いた導体形成用組成物
RU2485062C1 (ru) * 2011-10-18 2013-06-20 Учреждение образования "Белорусский государственный технологический университет" Стекло с наночастицами сульфида свинца для просветляющихся фильтров
JP6514894B2 (ja) 2011-11-23 2019-05-15 クォークスター・エルエルシー 光を非対称に伝搬させる発光デバイス
US9915410B2 (en) 2012-09-13 2018-03-13 Quarkstar Llc Light-emitting devices with reflective elements
CN110274162A (zh) 2012-09-13 2019-09-24 夸克星有限责任公司 具有远程散射元件和全内反射提取器元件的发光设备
US9683710B2 (en) 2013-03-07 2017-06-20 Quarkstar Llc Illumination device with multi-color light-emitting elements
US9752757B2 (en) 2013-03-07 2017-09-05 Quarkstar Llc Light-emitting device with light guide for two way illumination
US10811576B2 (en) 2013-03-15 2020-10-20 Quarkstar Llc Color tuning of light-emitting devices
CN104676299A (zh) * 2013-11-29 2015-06-03 广东德豪润达电气股份有限公司 白光led光源组件及其生产方法
DE102017200413A1 (de) 2016-02-02 2017-08-03 Schott Ag Röntgen- und Gamma-Strahlen abschirmendes Glas
CN106587596B (zh) * 2016-10-31 2019-08-27 中国科学院西安光学精密机械研究所 重火石zf系列空间耐辐照光学玻璃及其制备方法
CN113754275A (zh) * 2021-09-23 2021-12-07 成都光明光电有限责任公司 防辐射玻璃

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4018613A (en) * 1976-02-06 1977-04-19 Corning Glass Works Diode encapsulation glass
DE3228826C2 (de) * 1982-08-02 1986-09-25 Schott Glaswerke, 6500 Mainz Hochabsorbierendes Pb-haltige Gläser für Kathodenstrahlröhrenbildschirme
FR2533911B1 (fr) * 1982-09-30 1986-07-25 Corning Glass Works Verres d'alumino-fluoro-borosilicate de plomb moulables
DE3404363A1 (de) * 1984-02-08 1985-08-14 Schott Glaswerke, 6500 Mainz Hoch pbo-haltige glaeser im system sio(pfeil abwaerts)2(pfeil abwaerts)pbo-m(pfeil abwaerts)2(pfeil abwaerts)o mit erhoehter chemischer bestaendigkeit
DE3504558A1 (de) * 1985-02-11 1986-08-14 Schott Glaswerke, 6500 Mainz Optisches glas mit spannungsoptischem koeffizienten, der proportional zur wellenlaenge elektromagnetischer strahlung ist
US4983551A (en) * 1988-08-13 1991-01-08 Galileo Electro-Optics Corp. Channel electron multipliers
US5224001A (en) * 1989-11-29 1993-06-29 Matsushita Electric Industrial Co., Ltd. Magnetic head
US5034354A (en) * 1990-05-16 1991-07-23 Corning Incorporated Alkali-free multichannel plate and glass
US5162826A (en) * 1991-06-17 1992-11-10 Corning Incorporated High index ophthalmic glasses
JPH054836A (ja) * 1991-06-24 1993-01-14 Hitachi Metals Ltd 磁気ヘツド組立用ボンデイングガラス及び磁気ヘツド
US6432854B1 (en) * 1994-02-07 2002-08-13 Nikon Corporation Optical glass for polarizing optical system, production process therefor and polarizing beam splitter
WO1995021137A1 (fr) * 1994-02-07 1995-08-10 Nikon Corporation Verre optique pour systemes optiques polarisants, procede de fabrication correspondant et dispositif de fractionnement du faisceau polarisant
US6227670B1 (en) * 1995-03-06 2001-05-08 Nikon Corporation Projection type display apparatus
US6150027A (en) * 1995-06-16 2000-11-21 Hitachi, Ltd Glass composition, structure, and apparatus using the same
JP4016146B2 (ja) * 1996-04-01 2007-12-05 ソニー株式会社 ガラス組成物及びガラス組成物を用いた磁気ヘッド
JP4278209B2 (ja) * 1997-11-25 2009-06-10 Hoya株式会社 光学素子及びその製造方法
US6497962B1 (en) * 1999-11-19 2002-12-24 Asahi Glass Company, Limited Low melting point glass for covering electrodes, and plasma display device
WO2001040127A1 (fr) * 1999-11-30 2001-06-07 Kabushiki Kaisha Ohara Verre optique
US6756334B2 (en) * 2001-05-29 2004-06-29 Kabushiki Kaisha Ohara Optical glass
KR100495488B1 (ko) * 2002-12-07 2005-06-16 엘지마이크론 주식회사 플라즈마 디스플레이 패널의 후면판
DE102004001458B4 (de) * 2004-01-08 2012-01-19 Schott Ag Glas mit deutlich verbesserter Stabilität gegen Strahlenbeschädigungen, ein Verfahren zu seiner Herstellung sowie dessen Verwendung

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO03064340A3 *

Also Published As

Publication number Publication date
US20050075234A1 (en) 2005-04-07
CN1622922A (zh) 2005-06-01
JP2005515954A (ja) 2005-06-02
RU2004126253A (ru) 2006-02-10
AU2003210130A1 (en) 2003-09-02
DE10203226A1 (de) 2003-09-04
WO2003064340A3 (de) 2003-10-16
DE10390245D2 (de) 2005-01-05
WO2003064340A2 (de) 2003-08-07

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