USRE37920E1 - Flat panel display - Google Patents

Flat panel display Download PDF

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USRE37920E1
USRE37920E1 US09/060,741 US6074198A USRE37920E US RE37920 E1 USRE37920 E1 US RE37920E1 US 6074198 A US6074198 A US 6074198A US RE37920 E USRE37920 E US RE37920E
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bao
cao
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mgo
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Dawne M. Moffatt
Dean V. Neubauer
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Corning Inc
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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
    • C03C3/076Glass compositions containing silica with 40% to 90% silica, by weight
    • C03C3/083Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound
    • C03C3/085Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound containing an oxide of a divalent metal
    • 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
    • C03C10/00Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition
    • 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
    • C03C3/076Glass compositions containing silica with 40% to 90% silica, by weight
    • C03C3/089Glass compositions containing silica with 40% to 90% silica, by weight containing boron
    • C03C3/091Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods
    • G02F1/133337Layers preventing ion diffusion, e.g. by ion absorption

Definitions

  • a flat panel display device having an aluminosilicate glass panel exhibiting physical and chemical properties necessary for such devices and their production.
  • flat panel displays have received a great deal of attention recently. Thus far, much of the attention has centered on small units such as are used in laptop computers. However, increasing consideration is being given to larger units for information and entertainment applications.
  • One particular form of flat panel display is known as a liquid crystal display.
  • Liquid crystal displays are flat panel display devices which depend upon external sources of light for illumination. They may take one of two basic matrix types, intrinsic or extrinsic matrix addressed.
  • the intrinsic matrix type relies upon the threshold properties of the liquid crystal material.
  • the extrinsic, or active matrix (AM), type has an array of diodes, metal-insulator-metal (MIM) devices, or thin film transistors (TFTs), that supplies an electronic switch to each pixel.
  • MIM metal-insulator-metal
  • TFTs thin film transistors
  • two sheets of glass form the structure of the display.
  • the separation between the two sheets is the critical gap dimension, of the order of 5-10 ⁇ m.
  • the glass sheets must be transparent, and must withstand the chemical conditions to which they are exposed during display processing. Otherwise, the needs of the two matrix types differ.
  • Intrinsically addressed LCDs are fabricated using thin film deposition techniques at temperatures ⁇ 350° C., followed by photolithographic patterning. As a result, the substrate requirements therefore are often the same as those for segmented displays. Soda-lime-silica glass with a barrier layer has proven to be adequate for most needs.
  • a high performance version of intrinsically addressed LCDs the super twisted nematic (STN) type, has an added requirement of extremely precise flatness for the purpose of holding the gap dimensions uniform. Because of that requirement, soda-lime-silica glass used for those displays must be polished. Alternatively, a precision formed, barium aluminoborosilicate glass, marketed by Corning Incorporated, Corning, N.Y. as Code 7059, may be used without polishing.
  • Extrinsically addressed LCDs can be further subdivided into two categories; viz., one based on MIM or amorphous silicon (a-Si) devices, and the other based on polycrystalline silicon (poly-Si) devices.
  • the substrate requirements of the MIM or a-Si type are similar to the STN application.
  • Corning Code 7059 sheet glass is the preferred substrate because of its very low sodium content, i.e., less than 0.1% Na 2 O by weight, its dimensional precision, and its commercial availability.
  • Devices formed from poly-Si are processed at higher temperatures than those that are employed with a-Si TFTs.
  • Substrates capable of use temperatures (taken to be 25° C. below the strain point of the glass) of 600°-800° C. are demanded.
  • the actual temperature required is mandated by the particular process utilized in fabricating the TFTs.
  • Those TFTs with deposited gate dielectrics require 600°-650° C., while those with thermal oxides call for about 800° C.
  • the glass must be essentially free of intentionally added alkali metal oxide to avoid the possibility that alkali metal from the substrate can migrate into the transistor matrix;
  • the glass substrate must be sufficiently chemically durable to withstand the reagents used in the TFT matrix deposition process
  • the expansion mismatch between the glass and the silicon present in the TFT array must be maintained at a relatively low level even as processing temperatures for the substrates increase;
  • the glass must be capable of being produced in high quality thin sheet form at low cost; that is, it must not require extensive grinding and polishing to secure the necessary surface finish.
  • Corning Code 7059 glass is currently employed in the fabrication of LCDs. That glass, consisting essentially, in weight percent, of about 50% SiO 2 , 15% B 2 O 3 , 10% Al 2 O 3 , and 24% BaO, is nominally free of alkali metal oxides, and exhibits a linear coefficient of thermal expansion, CTE, (25°-300° C.) of about 46 ⁇ 10 ⁇ 7 /°C. and a viscosity at the liquidus temperature in excess of 60,000 Pa.s (600,000 poises).
  • CTE linear coefficient of thermal expansion
  • the high liquidus viscosity of the glass enables it to be drawn into sheet via the overflow downdraw sheet processing technique, but its relatively low strain point ( ⁇ 593° C.) is adequate only for processing a-Si devices and not for poly-Si devices.
  • the glasses had to be adapted to use in fabricating poly-Si devices. Next, they had to be capable of being formed into sheet by the overflow downdraw process. Finally, they had to have linear CTEs that closely matched silicon.
  • a recent advance in liquid crystal technology termed “chip-on-glass” (COG) has further emphasized the need for the substrate glass to closely match silicon in thermal expansion.
  • the initial LCD devices did not have their driver chips mounted on the substrate glass. Instead, the silicon chips were mounted remotely and were connected to the LCD substrate circuitry with compliant or flexible wiring.
  • TAB Tape Automatic Bonding
  • TAB decreased cost while improving reliability and increasing the permitted density of the conductors to a pitch of approximately 200 ⁇ m—all significant factors.
  • COG provides further improvement over TAB with respect to those three factors.
  • the substrate glass must demonstrate a linear coefficient of thermal expansion closely matching that of silicon; i.e., the glass must exhibit a linear coefficient of thermal expansion (0°-300° C.) between 31-44 ⁇ 10 ⁇ 7 /°C., most preferably 32-40 ⁇ 10 ⁇ 7 /°C.
  • the float process involves drawing a continuous sheet of glass over the surface of a molten metal, such as molten tin.
  • a molten metal such as molten tin.
  • the surface contacting the molten metal is not exposed during drawing, and hence is relatively smooth and free from defects. This has the virtue of requiring finishing of only one surface.
  • a further purpose is to provide such panels that can be fabricated by a method other than the overflow downdraw process, such as the float process.
  • the present invention resides in a flat panel display comprising an aluminosilicate glass panel that exhibits a strain point higher than 640° C., CTEs in the range of 31-57 ⁇ 10 ⁇ 7 /°C., a weight loss less than 20 mg/cm 2 after immersion for 24 hours in an aqueous 5% by weight HCl solution at 95° C., that is nominally free from alkali metal oxides and has a composition consisting essentially, calculated in weight percent on the oxide basis, of 49-67% SiO 2 , at least 6% Al 2 O 3 , the Al 2 O 3 being 6- 14% in conjunction with 55-67% SiO 3 and 16-23% in conjunction with 49-58% SiO 2 , SiO 2 +Al 2 O 3 >68%, 0-15% B 2 O 3 , at least one alkaline earth metal oxide selected from the group consisting of, in the preparations indicated, 0-21% BaO, 0-15% SrO, 0- 18% CaO, 0-8% MgO and
  • the invention further resides in a method of producing a glass panel for a flat panel display which comprises melting a batch for an aluminosilicate glass consisting essentially of, as calculated in percent by weight on an oxide basis, 49-67% SiO 2 , at least 6% Al 2 O 3 , the Al 2 O 3 being 6-14% in conjunction with 55-67% SiO 2 and 16-23% in conjunction with 49-58% SiO 2 , SiO 2 +Al 2 O 3 >68%, 0-15% B 2 O 3 , at least one alkaline earth metal oxide selected from the group consisting of, in the indicated proportions, 0-21% BaO, 0-15% SrO, 0-18% CaO, 0-8% MgO and 12-30% BaO+CaO, SrO+MgO, and drawing a thin sheet of molten glass from the melt.
  • the invention also contemplates an aluminosilicate glass exhibiting a strain point higher than 640° C., a weight loss less than 20 mg/cm 2 after immersion for 24 hours in an aqueous 5% by weight HCl solution at 95° C., a CTE between 31 and 57 ⁇ 10 ⁇ 7 /°C., nominally free of alkali metal oxides and having a composition consisting essentially of, as calculated in percent by weight on an oxide basis, 49-67% SiO 2 , at least 6% Al 2 O 3 , the Al 2 O 3 being 6-14% in conjunction with 55-67% SiO 2 and 16-23% in conjunction with 49-58% SiO 2 , SiO 2 +Al 2 O 3 >68%, 0-15% B 2 O 3 , at least one alkaline earth metal oxide selected from the group consisting of, in the proportions indicated, 0-21% BaO, 0-15% SrO, 0-18% CaO, 0-8% MgO and 12-30% BaO+CaO+
  • the invention arose from a desire for flat display device panels that could be produced by a method that did not impose the requirement of the overflow downdraw process. In particular, it was desired to avoid the need for the very high viscosity at the liquidus temperature of over 60,000 Pa.s (600,000 poises).
  • SiO 2 and Al 2 O 3 are the glass-forming oxides. At least 49% SiO 2 and 6% Al 2 O 3 are required for this purpose, as well as to provide the desired high strain point. Glass melting tends to become difficult with SiO 2 contents greater than 67% and Al 2 O 3 contents greater than 23%.
  • SiO 2 and Al 2 O 3 are also of concern with respect to glass durability. In this respect, however, the SiO 2 and Al 2 O 3 contents are interdependent. Thus, with Al 2 O 3 contents in the range of 6-14%, a SiO 2 content of at least 55%, and preferably at least 60%, is necessary to provide the required chemical durability. With an Al 2 O 3 content in the range of 16-23%, the SiO 2 content may be as low as 49% while obtaining adequate durability. The total SiO 2 +Al 2 O 3 content should be greater than about 68% to achieve the desired durability.
  • B 2 O 3 tends to soften the glass, that is, lower the melting temperature and facilitate melting. However, it lowers the strain point and is detrimental to durability, particularly in large amounts. Consequently, the B 2 O 3 content should not exceed about 15%, and preferably is no more than 8%.
  • the alkaline earth metals increase CTE in this order Ba>Sr>Ca>Mg with BaO having the greatest effect and MgO the least.
  • any benefits, such as to refractive index or durability, may be obtained otherwise.
  • Alkali metals and halides tend to poison liquid crystal fluids, and hence are avoided except as unavoidable impurities.
  • weight loss when a glass sample is immersed in a 5% by weight solution of HCl for 24 hours at 95° C.
  • the weight loss must be less than 20 mg/cm 2 , is preferably below 5, and most preferably below one mg/cm 2 .
  • CTE coefficient of thermal expansion
  • the other CTE level is based on a desire to match silicon, thus permitting direct chip attachment.
  • Silicon has a CTE of 36 ⁇ 10 ⁇ 7 /°C. Accordingly, a CTE range for glass panels may be 31-44 ⁇ 10 ⁇ 7 /°C., preferably 32-40 ⁇ 10 ⁇ 7 /°C.
  • the invention contemplates a method of producing panels for LCD devices by melting a glass as described above, forming sheet glass from the melt by such processes as the float process, redrawing or rolling, and cutting the sheet into panel size.
  • Table I reports a number of glass compositions.
  • the compositions are expressed in terms of parts by weight on the oxide basis, illustrating the compositional parameters of the present inventive glasses.
  • the sum of the individual components closely approximates 100, being slightly lower due to omission of a fining agent, such as As 2 O 3 .
  • a fining agent such as As 2 O 3 .
  • the listed values may be considered to reflect weight percent.
  • the actual batch materials may comprise the desired oxides. They may also comprise other compounds, which, when melted together with the other batch constituents, will be converted into the desired oxides in the proper proportions.
  • CaCO 3 and BaCO 3 can supply the source of CaO and BaO, respectively.
  • the melts were stirred in both directions, i.e., both clockwise and counterclockwise.
  • the melts were then poured onto steel plates to make glass slabs having the approximate dimensions 18′′ ⁇ 6′′ ⁇ 0.5′′ ( ⁇ 45.7 ⁇ 15.2 ⁇ 1.3 cm). Those slabs were then transferred immediately to an annealer operating at about 725° C.
  • inventive glasses are quite capable of being melted and formed utilizing large scale, commercial glass melting and forming equipment.
  • fining agents such as the oxides of arsenic and antimony, may be added in customary amounts. The small residual remaining in the glass has no substantial effect upon the physical properties of the glass.
  • Table I also recites measurements of several chemical and physical properties determined on the glasses in accordance with measuring techniques conventional in the glass art.
  • the linear coefficient of thermal expansion (CTE) over the temperature range 0°-300° C. is expressed in terms of ⁇ 10 ⁇ 7 /°C.
  • the softening point (S.P.), and the strain point (St.P) are expressed in terms of °C., and were determined via fiber elongation.
  • the durability (Dur) in HCl was evaluated by determining the weight loss (mg/cm 2 ) after immersion in a bath of aqueous 5% by weight HCl operating at 95° C. for 24 hours.
  • Table IA records the same glass compositions but reported in terms of mole percent on the oxide basis.
  • compositions 1, 4 and 9 are quite similar, except that 1 has a substantial SrO content, 4 has a substantial CaO content, and 9 omits B 2 O 3 in favor of BaO. The consequence is a continuously higher strain point from 1 to 4 to 9, with 1 being marginally acceptable.
  • compositions 11 and 12 indicate that substituting alkaline earth metal oxides has an enormous effect on durability. Also, comparing compositions 1 and 6 suggests the beneficial effect of omitting B 2 O 3 in favor of alkaline earth metal oxides.
  • a preferred CTE range for glass panels compatible with Code 7059 glass is 45-50 ⁇ 10 ⁇ 7 /°C.
  • Glasses in aluminosilicate sub-families A′ and B′ have CTEs in this range and have compositions consisting essentially of, as calculated in weight percent on an oxide basis:
  • compositions 13, 14 and 15 exemplify the A′ sub-family
  • 16, 17 and 18 exemplify the B′ sub-family.
  • CTE ranges for glass panels adapted to use with silicon have been noted as having a CTE range of 32-40 ⁇ 10 ⁇ 7 /°C.
  • Glasses in aluminosilicate sub-families C′ and D′ have CTEs within that range and have compositions that consist essentially of, as calculated in weight percent on an oxide basis:
  • compositions 19, 20 and 21 sets forth exemplary compositions within these sub-families.
  • the C′ sub-family is exemplified by compositions 19, 20 and 21, while the D′ sub-family is exemplified by compositions 22, 23 and 24.
  • a glass panel for a flat panel display has a strain point greater than 660° C. and has a weight loss less than 1 mg/cm 2 in the HCl test described earlier.
  • glasses having compositions falling within two aluminosilicate sub-families meet these preferred qualifications.
  • the two families, E and F have compositions consisting essentially of, as calculated in weight percent on an oxide basis:
  • a further preferred embodiment constitutes glass panels having a density less than 2.5 grams/cc. Glasses meeting this requirement fall within an aluminosilicate sub-family G having the following constituent ranges consisting essentially of, as analyzed on an oxide basis:

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Abstract

A flat panel display comprising an aluminosilicate glass panel that exhibits a strain point higher than 640° C., a weight loss less than 20 mg/cm2 after immersion for 24 hours in an aqueous 5% by weight HCl solution at 95° C., a CTE in the range of 31-57×10−7/° C., is nominally free of alkali metal oxides and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, 49-67% SiO2, at least 6% Al2O3, the Al2O3 being 6-14% in conjunction with 55-67% SiO2 and 16-23% in conjunction with 49-58% SiO2, SiO2+Al2O3>68%, 0-15% B2O3, at least one alkaline earth metal oxide selected from the group consisting of, in the proportions indicated, 0-21% BaO, 0-15% SrO, 0-18% CaO, 0-8% MgO and 12-30% BaO+CaO+SrO+MgO.

Description

This application is a Continuation-In-Part of U.S. Ser. No. 08/212,060, filed Mar. 14, 1994, now abandoned.
FIELD OF THE INVENTION
A flat panel display device having an aluminosilicate glass panel exhibiting physical and chemical properties necessary for such devices and their production.
BACKGROUND OF THE INVENTION
Flat panel displays have received a great deal of attention recently. Thus far, much of the attention has centered on small units such as are used in laptop computers. However, increasing consideration is being given to larger units for information and entertainment applications. One particular form of flat panel display is known as a liquid crystal display.
Liquid crystal displays (LCDs) are flat panel display devices which depend upon external sources of light for illumination. They may take one of two basic matrix types, intrinsic or extrinsic matrix addressed. The intrinsic matrix type relies upon the threshold properties of the liquid crystal material. The extrinsic, or active matrix (AM), type has an array of diodes, metal-insulator-metal (MIM) devices, or thin film transistors (TFTs), that supplies an electronic switch to each pixel.
In both cases, two sheets of glass form the structure of the display. The separation between the two sheets is the critical gap dimension, of the order of 5-10 μm. The glass sheets must be transparent, and must withstand the chemical conditions to which they are exposed during display processing. Otherwise, the needs of the two matrix types differ.
Intrinsically addressed LCDs are fabricated using thin film deposition techniques at temperatures ≦350° C., followed by photolithographic patterning. As a result, the substrate requirements therefore are often the same as those for segmented displays. Soda-lime-silica glass with a barrier layer has proven to be adequate for most needs.
A high performance version of intrinsically addressed LCDs, the super twisted nematic (STN) type, has an added requirement of extremely precise flatness for the purpose of holding the gap dimensions uniform. Because of that requirement, soda-lime-silica glass used for those displays must be polished. Alternatively, a precision formed, barium aluminoborosilicate glass, marketed by Corning Incorporated, Corning, N.Y. as Code 7059, may be used without polishing.
Extrinsically addressed LCDs can be further subdivided into two categories; viz., one based on MIM or amorphous silicon (a-Si) devices, and the other based on polycrystalline silicon (poly-Si) devices. The substrate requirements of the MIM or a-Si type are similar to the STN application. Corning Code 7059 sheet glass is the preferred substrate because of its very low sodium content, i.e., less than 0.1% Na2O by weight, its dimensional precision, and its commercial availability.
Devices formed from poly-Si, however, are processed at higher temperatures than those that are employed with a-Si TFTs. Substrates capable of use temperatures (taken to be 25° C. below the strain point of the glass) of 600°-800° C. are demanded. The actual temperature required is mandated by the particular process utilized in fabricating the TFTs. Those TFTs with deposited gate dielectrics require 600°-650° C., while those with thermal oxides call for about 800° C.
Both a-Si and poly-Si processes demand precise alignment of successive photolithographic patterns, thereby necessitating that the thermal shrinkage of the substrate be kept low. The higher temperatures required for poly-Si mandate the use of glasses exhibiting higher strain points than soda-lime-silica glass and Corning Code 7059 glass in order to avoid thermal deformation of the sheet during processing. As can be appreciated, the lower the strain point, the greater this dimensional change. Thus, there has been considerable research to develop glasses demonstrating high strain points so that thermal deformation is minimized during device processing at temperatures greater than 600° C., and preferably, higher than 650° C.
U.S. Pat. No. 4,824,808 (Dumbaugh, Jr.) lists four properties which have been deemed mandatory for a glass to exhibit in order to fully satisfy the needs of a substrate for LCDs:
First, the glass must be essentially free of intentionally added alkali metal oxide to avoid the possibility that alkali metal from the substrate can migrate into the transistor matrix;
Second, the glass substrate must be sufficiently chemically durable to withstand the reagents used in the TFT matrix deposition process;
Third, the expansion mismatch between the glass and the silicon present in the TFT array must be maintained at a relatively low level even as processing temperatures for the substrates increase; and
Fourth, the glass must be capable of being produced in high quality thin sheet form at low cost; that is, it must not require extensive grinding and polishing to secure the necessary surface finish.
That last requirement is most difficult to achieve inasmuch as it demands a sheet glass production process capable of producing essentially finished glass sheet. Currently, the overflow downdraw sheet manufacturing process is employed. This process is described in U.S. Pat. No. 3,338,696 (Dockerty) and U.S. Pat. No. 3,682,609 (Dockerty). That process requires a glass exhibiting a very high viscosity at the liquidus temperature plus long term stability, e.g., periods of 30 days, against devitrification at melting and forming temperatures.
Corning Code 7059 glass, supra, is currently employed in the fabrication of LCDs. That glass, consisting essentially, in weight percent, of about 50% SiO2, 15% B2O3, 10% Al2O3, and 24% BaO, is nominally free of alkali metal oxides, and exhibits a linear coefficient of thermal expansion, CTE, (25°-300° C.) of about 46×10−7/°C. and a viscosity at the liquidus temperature in excess of 60,000 Pa.s (600,000 poises). The high liquidus viscosity of the glass enables it to be drawn into sheet via the overflow downdraw sheet processing technique, but its relatively low strain point (˜593° C.) is adequate only for processing a-Si devices and not for poly-Si devices.
Accordingly, extensive research has been directed at developing glasses designed to meet at least three general requirements. Initially, the glasses had to be adapted to use in fabricating poly-Si devices. Next, they had to be capable of being formed into sheet by the overflow downdraw process. Finally, they had to have linear CTEs that closely matched silicon.
The fruits of such research are reported, for example, in U.S. Pat. Nos. 4,409,337; 4,824,808; 5,116,787; 5,116,788; and 5,116,789, all issued in the name of W. H. Dumbaugh, Jr. The properties of these glasses, as well as their shortcomings, are reviewed in pending application Ser. No. 08/008,560 filed in the names of Dumbaugh, Jr. et al. and assigned to the assignee of the subject application.
A recent advance in liquid crystal technology termed “chip-on-glass” (COG) has further emphasized the need for the substrate glass to closely match silicon in thermal expansion. Thus, the initial LCD devices did not have their driver chips mounted on the substrate glass. Instead, the silicon chips were mounted remotely and were connected to the LCD substrate circuitry with compliant or flexible wiring. As LCD device technology improved and as the devices became larger, these flexible mountings became unacceptable, both because of cost and of uncertain reliability. This situation led to Tape Automatic Bonding (TAB) of the silicon chips. In that process the silicon chips and electrical connections to the chips were mounted on a carrier tape, that subassembly was mounted directly on the LCD substrate, and thereafter the connection to the LCD circuitry was completed. TAB decreased cost while improving reliability and increasing the permitted density of the conductors to a pitch of approximately 200 μm—all significant factors. COG, however, provides further improvement over TAB with respect to those three factors. Hence, as the size and quality requirements of LCD devices increase, COG is demanded for those devices dependent upon the use of integrated circuit silicon chips. For that reason, the substrate glass must demonstrate a linear coefficient of thermal expansion closely matching that of silicon; i.e., the glass must exhibit a linear coefficient of thermal expansion (0°-300° C.) between 31-44×10−7/°C., most preferably 32-40×10−7/°C.
The high viscosity value at the liquidus required for the overflow downdraw process, 600,000 poises (60,000 Pa.s), has been difficult to obtain in conjunction with the several other properties required for poly-Si devices. Consequently, attention has been given to other sheet-forming processes where the viscosity factor is not of such great significance. These include the float process and a redraw process.
The float process involves drawing a continuous sheet of glass over the surface of a molten metal, such as molten tin. The surface contacting the molten metal is not exposed during drawing, and hence is relatively smooth and free from defects. This has the virtue of requiring finishing of only one surface. It is a primary purpose of the present invention to provide panels for flat panel display devices, in particular, LCD devices embodying poly-Si chips. A further purpose is to provide such panels that can be fabricated by a method other than the overflow downdraw process, such as the float process.
SUMMARY OF THE INVENTION
The present invention resides in a flat panel display comprising an aluminosilicate glass panel that exhibits a strain point higher than 640° C., CTEs in the range of 31-57×10−7/°C., a weight loss less than 20 mg/cm2 after immersion for 24 hours in an aqueous 5% by weight HCl solution at 95° C., that is nominally free from alkali metal oxides and has a composition consisting essentially, calculated in weight percent on the oxide basis, of 49-67% SiO2, at least 6% Al2O3, the Al2O3 being 6- 14% in conjunction with 55-67% SiO3 and 16-23% in conjunction with 49-58% SiO2, SiO2+Al2O3>68%, 0-15% B2O3, at least one alkaline earth metal oxide selected from the group consisting of, in the preparations indicated, 0-21% BaO, 0-15% SrO, 0- 18% CaO, 0-8% MgO and 12-30% BaO+CaO+SrO+MgO.
The invention further resides in a method of producing a glass panel for a flat panel display which comprises melting a batch for an aluminosilicate glass consisting essentially of, as calculated in percent by weight on an oxide basis, 49-67% SiO2, at least 6% Al2O3, the Al2O3 being 6-14% in conjunction with 55-67% SiO2 and 16-23% in conjunction with 49-58% SiO2, SiO2+Al2O3>68%, 0-15% B2O3, at least one alkaline earth metal oxide selected from the group consisting of, in the indicated proportions, 0-21% BaO, 0-15% SrO, 0-18% CaO, 0-8% MgO and 12-30% BaO+CaO, SrO+MgO, and drawing a thin sheet of molten glass from the melt.
The invention also contemplates an aluminosilicate glass exhibiting a strain point higher than 640° C., a weight loss less than 20 mg/cm2 after immersion for 24 hours in an aqueous 5% by weight HCl solution at 95° C., a CTE between 31 and 57×10−7/°C., nominally free of alkali metal oxides and having a composition consisting essentially of, as calculated in percent by weight on an oxide basis, 49-67% SiO2, at least 6% Al2O3, the Al2O3 being 6-14% in conjunction with 55-67% SiO2 and 16-23% in conjunction with 49-58% SiO2, SiO2+Al2O3>68%, 0-15% B2O3, at least one alkaline earth metal oxide selected from the group consisting of, in the proportions indicated, 0-21% BaO, 0-15% SrO, 0-18% CaO, 0-8% MgO and 12-30% BaO+CaO+SrO+MgO.
DESCRIPTION OF THE INVENTION
The invention arose from a desire for flat display device panels that could be produced by a method that did not impose the requirement of the overflow downdraw process. In particular, it was desired to avoid the need for the very high viscosity at the liquidus temperature of over 60,000 Pa.s (600,000 poises).
At the same time, certain other requirements must be met, however. These include a glass strain point greater than 640° C., good chemical durability, freedom from alkali metals and a controlled coefficient of thermal expansion (CTE).
We have found that these several requirements may be met by members of a nominally alkali metal-free, aluminosilicate glass family having compositions, calculated on an oxide basis, consisting essentially of 49-67% SiO2, at least 6% Al2O3, the Al2O3 being 6-14% Al2O3 in conjunction with 55-67% SiO2, and 16-23% in conjunction with 49-58% SiO2, SiO2+Al2O3>68%, 0-15% B2O, at least one alkaline earth metal oxide selected from the group consisting of, in the proportions indicated, of 0-21% BaO, 0-15% SrO, 0-18% CaO, 0-8% MgO and 12-30% BaO+SrO+CaO+MgO.
Compliance with those specified composition intervals has been found necessary in order to obtain glasses illustrating the desired matrix of chemical, forming, and physical properties, as is demonstrated below.
SiO2 and Al2O3 are the glass-forming oxides. At least 49% SiO2 and 6% Al2O3 are required for this purpose, as well as to provide the desired high strain point. Glass melting tends to become difficult with SiO2 contents greater than 67% and Al2O3 contents greater than 23%.
SiO2 and Al2O3 are also of concern with respect to glass durability. In this respect, however, the SiO2 and Al2O3 contents are interdependent. Thus, with Al2O3 contents in the range of 6-14%, a SiO2 content of at least 55%, and preferably at least 60%, is necessary to provide the required chemical durability. With an Al2O3 content in the range of 16-23%, the SiO2 content may be as low as 49% while obtaining adequate durability. The total SiO2+Al2O3 content should be greater than about 68% to achieve the desired durability.
B2O3 tends to soften the glass, that is, lower the melting temperature and facilitate melting. However, it lowers the strain point and is detrimental to durability, particularly in large amounts. Consequently, the B2O3 content should not exceed about 15%, and preferably is no more than 8%.
Where silicon chips are to be mounted on the glass, and a CTE of 31-44×10−7/°C. is necessary, BaO content is preferably maintained low. Other alkaline earth metal oxides and/or Al2O3 may be substituted.
In general, the alkaline earth metals increase CTE in this order Ba>Sr>Ca>Mg with BaO having the greatest effect and MgO the least.
In addition to the constituents recited above, a variety of optional constituents are also contemplated. These include TiO2, ZrO2, ZnO, La2O3, Ta2O5, Nb2O5 and Y2O3. Preferably, these oxides are not present in amounts exceeding about 5% by weight since they tend to increase density and may decrease the strain point. In general, any benefits, such as to refractive index or durability, may be obtained otherwise.
Alkali metals and halides tend to poison liquid crystal fluids, and hence are avoided except as unavoidable impurities.
A commonly accepted measure of chemical durability is weight loss when a glass sample is immersed in a 5% by weight solution of HCl for 24 hours at 95° C. For present purposes, the weight loss must be less than 20 mg/cm2, is preferably below 5, and most preferably below one mg/cm2.
There are two levels of coefficient of thermal expansion (CTE) that are relevant in glass panels for display panels, particularly LCD devices. One level is based on what had become a standard in the trade, Code 7059 glass. That glass has a CTE of 46×10−7/°C., and a CTE range of 44-57×10−7/°C. has been considered compatible. Preferably, the range is 45-50×10−7/°C.
We have found two aluminosilicate sub-families A and B that provide CTE values at this level. Glasses having compositions that fall within these sub-families consist essentially of, as calculated in weight percent on an oxide basis:
A B
SiO2 50-57 55-67  
Al2O3 16-22 6-14 
B2O3   0-5.5 0-7.5
MgO 0.5-3   0-6.5
CaO   1-12.5  0-18.5
SrO 0.5-15   0-15.5
BaO  1-21 1-9.5
MgO + CaO + SrO + BaO 16.5-28  
The other CTE level is based on a desire to match silicon, thus permitting direct chip attachment. Silicon has a CTE of 36×10−7/°C. Accordingly, a CTE range for glass panels may be 31-44×10−7/°C., preferably 32-40×10−7/°C.
To achieve CTE values within these ranges, we have found two aluminosilicate sub-families C and D that meet the requirement. Glasses having compositions that fall within these sub-families consist essentially of, as calculated in weight percent on an oxide basis:
C D
SiO2 49-58 57-66 
Al2O3 17.5-23   8-14
B2O3   0-14.5 0-13
MgO 0-8  0-4.5
CaO 0-9 0-9 
SrO  0.4-13.5 0.5-13  
BaO  0-21 2-21
MgO + CaO + SrO + BaO 13-28
In another aspect, the invention contemplates a method of producing panels for LCD devices by melting a glass as described above, forming sheet glass from the melt by such processes as the float process, redrawing or rolling, and cutting the sheet into panel size.
DESCRIPTION OF PREFERRED EMBODIMENTS
Table I reports a number of glass compositions. The compositions are expressed in terms of parts by weight on the oxide basis, illustrating the compositional parameters of the present inventive glasses. The sum of the individual components closely approximates 100, being slightly lower due to omission of a fining agent, such as As2O3. Hence, for all practical purposes, the listed values may be considered to reflect weight percent.
The actual batch materials may comprise the desired oxides. They may also comprise other compounds, which, when melted together with the other batch constituents, will be converted into the desired oxides in the proper proportions. For example, CaCO3 and BaCO3 can supply the source of CaO and BaO, respectively.
Glass batches based on these compositions were compounded. The batches were tumble mixed together thoroughly to assist in obtaining a homogeneous melt, and then charged into platinum crucibles. After placing lids thereon, the crucibles were introduced into furnaces operating at temperatures of 1650° C. To assure the formation of glasses free form inclusions and cords, a two-step melting practice was undertaken. The batch was first melted for about 16 hours and stirred. It was thereafter poured as a fine stream into a bath of tap water to form finely-divided particles of glass. This process is termed “drigaging” in the glass art. In the second step, the finely-divided glass particles (after drying) were remelted at 1650° C. for about four hours. The melts were stirred in both directions, i.e., both clockwise and counterclockwise. The melts were then poured onto steel plates to make glass slabs having the approximate dimensions 18″×6″×0.5″ (˜45.7×15.2×1.3 cm). Those slabs were then transferred immediately to an annealer operating at about 725° C.
It must be recognized that the above description reflects a laboratory melting procedure only. Thus, the inventive glasses are quite capable of being melted and formed utilizing large scale, commercial glass melting and forming equipment. Where desired, fining agents, such as the oxides of arsenic and antimony, may be added in customary amounts. The small residual remaining in the glass has no substantial effect upon the physical properties of the glass.
Table I also recites measurements of several chemical and physical properties determined on the glasses in accordance with measuring techniques conventional in the glass art. The linear coefficient of thermal expansion (CTE) over the temperature range 0°-300° C. is expressed in terms of ×10−7/°C. The softening point (S.P.), and the strain point (St.P) are expressed in terms of °C., and were determined via fiber elongation. The durability (Dur) in HCl was evaluated by determining the weight loss (mg/cm2) after immersion in a bath of aqueous 5% by weight HCl operating at 95° C. for 24 hours.
TABLE I
1 2 3 4 5 6
SiO2 65 65.4 50.6 65 55.7 64.7
Al2O3 8.2 13 22.1 8.1 13.6 8.0
B2O3 7.8 6.0 5.8 5.1
MgO 3.1 0.3 3.0
CaO 18 7.1 5.7
SrO 13 0.4 12.8 5.2 12.9
BaO 2.2 20.7 8.2 2.2 9.3 7.7
CTE 38.6 38.9 41.3 48.5 46.8 49.4
St.P. 692 810 719 669 662 710
S.P. 1016 985 1003 1093 913 980
Dur. 2.73 0.03 6.65 0.69 0.22 0.01
7 8 9 10 11 12
SiO2 50.3 49.9 65.3 61.2 50.3 50.3
Al2O3 20.1 21.8 8.0 13.3 21.5 21.7
B2O3 0.6 5.5
MgO 0.6 5.9 5.9 2.9 5.8 3.1
CaO 6.4 0.3 8.7 0.6 9.2
SrO 0.4 0.5 12.6 5.9 0.4 13
BaO 20.9 20.5 7.0 2.4 20.2 2.2
CTE 48.7 43.5 44.9 43.4 43.6 51.3
St.P. 734 750 714 674 744 728
S.P. 1008 1013 993 928 1012 972
Dur. 4.9 5.4 0.01 0.07 5 240
Table IA records the same glass compositions but reported in terms of mole percent on the oxide basis.
TABLE IA
1 2 3 4 5 6
SiO2 72.43 80.18 63.56 68.05 64.03 75.05
Al2O3 5.33 9.38 16.36 5.02 9.20 5.48
B2O3 7.52 0.00 6.48 5.28 5.04 0.00
MgO 5.16 0.00 0.00 0.39 5.12 0.00
CaO 0.00 0.00 0.00 20.19 8.72 7.09
SrO 8.39 0.28 9.33 0.00 3.49 8.67
BaO 0.97 9.93 4.04 0.90 4.18 3.51
7 8 9 10 11 12
SiO2 63.65 62.03 73.34 61.56 62.46 56.70
Al2O3 14.96 15.94 5.27 10.57 15.70 14.39
B2O3 0.67 0.00 0.00 0.00 0.00 0.00
MgO 1.23 11.05 9.90 0.33 10.76 15.59
CaO 8.63 0.42 0.00 18.83 0.81 3.72
SrO 0.27 0.34 8.20 0.00 0.26 8.42
BaO 10.35 9.97 3.09 8.54 9.82 0.95
An examination of the above glasses illustrates the care in composition control that must be exercised in preparing glasses to provide the several properties that characterize the present invention. Thus, compositions 1, 4 and 9 are quite similar, except that 1 has a substantial SrO content, 4 has a substantial CaO content, and 9 omits B2O3 in favor of BaO. The consequence is a continuously higher strain point from 1 to 4 to 9, with 1 being marginally acceptable.
Comparisons also illustrate the effect of various oxide contents on durability. Thus, comparing compositions 11 and 12 indicates that substituting alkaline earth metal oxides has an enormous effect on durability. Also, comparing compositions 1 and 6 suggests the beneficial effect of omitting B2O3 in favor of alkaline earth metal oxides.
As noted earlier, a preferred CTE range for glass panels compatible with Code 7059 glass is 45-50×10−7/°C. Glasses in aluminosilicate sub-families A′ and B′ have CTEs in this range and have compositions consisting essentially of, as calculated in weight percent on an oxide basis:
A′ B′
SiO2 50-57 55-67  
Al2O3 16-20  6-<13 
B2O3   0-5.5 0-7.5
MgO   2-2.75 2-6.5
CaO  1-<7  0-17.5
SrO 0.5-15   0-14.5
BaO  1-21 2-9.5
TABLE II sets forth exemplary compositions within these sub-families. Compositions 13, 14 and 15 exemplify the A′ sub-family, while 16, 17 and 18 exemplify the B′ sub-family.
TABLE II
13 14 15 16 17 18
SiO2 56.1 52.9 53.9 65.5 56.6 66.9
Al2O3 17.0 18.2 18.0 8.1 11.2 6.1
B2O3 2.0 4.7 7.4
MgO 2.3 2.4 2.4 6.1 2.2 6.2
CaO 6.8 6.9 6.5 5.2 2.1
SrO 5 5.1 5.1 12.9 12.0 13.3
BaO 12.9 12.6 9.6 2.2 8.7 7.5
CTE 48.3 48.4 45.3 48.1 47.3 45.5
Strain 718 695 677 693 650 699
HCl 0.08 0.62 1.9 0.03 0.3 0.01
Density 2.31 2.80 2.70 2.70 2.72 2.73
Preferred CTE ranges for glass panels adapted to use with silicon have been noted as having a CTE range of 32-40×10−7/°C. Glasses in aluminosilicate sub-families C′ and D′ have CTEs within that range and have compositions that consist essentially of, as calculated in weight percent on an oxide basis:
C′ D′
SiO2 54-57  57-65.5
Al2O3 17.5-23   8-13
B2O3  5-15 4-13
MgO   2-2.75  2-3.5
CaO 1.5-<7   0-6.5
SrO 2-6 0-13
BaO 0.5-9.5 2-21
TABLE III sets forth exemplary compositions within these sub-families. The C′ sub-family is exemplified by compositions 19, 20 and 21, while the D′ sub-family is exemplified by compositions 22, 23 and 24.
TABLE III
19 20 21 22 23 24
SiO2 56.6 55.5 56.2 64.6 65 64.3
Al2O3 22.4 18.4 22.9 12.9 8.2 13
B2O3 7.8 9.3 5.9 4.4 7.8 4.4
MgO 2.3 2.3 2.4 2.2 3.1 2.2
CaO 3.4 6.9 4.9 6.3 6.3
SrO 4.9 5.0 5.0 0.8 13 1.2
BaO 2.6 2.6 2.7 8.8 2.2 8.7
CTE 32.2 40 35.4 38.8 38.6 38.8
Strain 692 666 706 683 692 686
HCl 1.8 2.6 0.8 0.02 2.7 0.02
Density 2.52 2.54 2.56 2.55 2.54 2.56
In a preferred embodiment of the invention, a glass panel for a flat panel display has a strain point greater than 660° C. and has a weight loss less than 1 mg/cm2 in the HCl test described earlier. We have found that glasses having compositions falling within two aluminosilicate sub-families meet these preferred qualifications. The two families, E and F, have compositions consisting essentially of, as calculated in weight percent on an oxide basis:
E F
SiO2 54-58 55-67
Al2O3 16-23  6-14
B2O3 0-6   0-7.5
MgO   2-4.5 0-7
CaO   1-12.5   0-18.5
SrO  2.5-15.5  0-15
BaO   0-14.5  1-21
MgO + CaO + SrO + BaO 15-27 18-28
TABLES IVE and IVF set forth, in approximate weight percent as analyzed on an oxide basis, the compositions and relevant properties of several representative examples of each sub-family, respectively:
TABLE IVE
25 26 27 28 29 30
SiO2 55.16 56.95 56.7 57.63 58.19 54.69
Al2O3 18.19 16.81 22.63 19.21 19.43 17.79
B2O3 0.95 0 0.997 5.33 5.35 0.94
MgO 2.23 2.25 2.31 2.6 2.67 2.17
CaO 1.46 4.7 6.7 8.63 8.76 1.39
SrO 13.06 4.82 4.86 5.5 5.61 14.25
BaO 8.94 14.47 5.77 1.09 0 8.76
CTE 45.4 46.8 41.8 42 41 46.8
Strain 731 724 748 684 688 722
HCl 0.074 0.06 0.57 0.16 0.48 0.11
Density 2.79 2.429 2.676 2.579 2.564 2.819
TABLE IVF
31 32 33 34 35 36
SiO2 55.7 55.53 56.9 65.49 66.93 66.85
Al2O3 13.6 13.3 13.03 8.14 6.1 6.23
B2O3 5.1 3.2 7.3 0 0 0
MgO 3 2.27 2.2 6.08 6.23 0.13
CaO 7.1 4.08 0 5.16 0 5.69
SrO 5.2 12.59 11.9 12.92 13.26 13.29
BaO 9.3 9.03 8.7 2.22 7.48 7.8
CTE 46.8 50.2 45 48.1 45.5 50.9
Strain 662 675 662 693 699 699
HCl 0.22 0.076 0.31 0.03 0.0134 0.0058
Density 2.705 2.799 2.692 2.695 2.725 2.741
A further preferred embodiment constitutes glass panels having a density less than 2.5 grams/cc. Glasses meeting this requirement fall within an aluminosilicate sub-family G having the following constituent ranges consisting essentially of, as analyzed on an oxide basis:
SiO2 54.8-57  
Al2O3 16.8-21.8
B2O3  0-14
MgO 2.2-2.5
CaO 1.5-9.5
SrO 4.5-5.5
BaO   0.1-14.5
MgO + CaO + SrO + BaO 12.5-27  
TABLE V sets forth in approximate weight percent, as analyzed on an oxide basis, compositions and relevant properties for representative examples:
TABLE V
37 38 39 40 41 42
SiO2 55.9 56.08 56.95 56.14 56.6 56.72
Al2O3 21.73 16.98 16.81 21.1 16.92 19.04
B2O3 9.76 0 0 1.06 0.99 9.73
MgO 2.45 2.28 2.25 2.28 2.31 2.37
CaO 2.36 6.78 4.7 5.59 9.4 6.95
SrO 5.13 5 4.82 4.84 4.78 5.07
BaO 2.67 12.86 14.47 8.99 8.91 0.12
CTE 31.2 48.3 46.8 43.6 49.3 37.6
Strain 680 718 724 737 710 670
HCl 3.36 0.08 0.06 0.27 0.15 4.15
Density 2.496 2.312 2.429 2.467 2.265 2.494

Claims (48)

We claim:
1. A flat panel display comprising an aluminosilicate glass panel that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5% by weight HCl solution at 95° C., a CTE in the range of 31-57×10−7/°C., is nominally free of alkali metal oxides and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, 49-67% SiO2, at least 6% Al2O3, and Al2O3 being 6-14% in conjunction with 55-67% SiO2 and 16-23% in conjunction with 49-58% SiO2, SiO2+Al2O3>68%, 0 to less than 8% B2O3, at least one alkaline earth metal oxide selected from the group consisting of, in the proportions indicated, 0-21% BaO, 0-15% SrO, 0-7.1% CaO, 0-8% MgO and 12-30% BaO+CaO+SrO+MgO.
2. A flat panel display in accordance with claim 1 in which the glass panel has a CTE in the range of 31-44×10−7/°C. and the glass is selected from a group of aluminosilicate sub-families consisting of glasses having compositions consisting essentially of, as calculated in weight percent on an oxide basis;
a. 49-58% SiO2, 17.5-23% Al2O3, 0 to less than 8% B2O3, 0-8% MgO, 0-7.1% CaO, 0.4-13.5% SrO, 0-21% BaO and MgO+CaO+SrO+BaO being 13-28%,
b. 57-66% SiO2, 8-14% Al2O3, 0 to less than 8% B2O3, 0-4.5% MgO, 0-7.1% CaO, 0.5-13% SrO and 2-21% BaO.
3. A flat panel display in accordance with claim 2 in which the glass panel has a CTE in the range of 32-40×10−7/°C. and the aluminosilicate sub-families consist essentially of:
a. 54-57% SiO2, 17.5-23% Al2O3, 5 to less than 8% B2O3, 2-2.75% MgO, 1.5- <7% CaO, 2-6% SrO and 0.5-9.5% BaO,
b. 57-65.5% SiO2, 8-13% Al2O3, 4 to less than 8% B2O3, 2-3.5% MgO, 0-6.5% CaO, 0-13% SrO and 2-21% BaO.
4. A flat panel display in accordance with claim 1 in which the glass panel has a CTE in the range of 44-57×10−7/°C. and the glass is selected from a group of aluminosilicate sub-families consisting of glasses having compositions consisting essentially of, as calculated in weight percent on an oxide basis:
a. 50-57% SiO2, 16-22% Al2O3, 0-5.5% B2O3, 0.5-3% MgO, 1-7.1% CaO, 0.5-15% SrO and 1-21% BaO,
b. 55-67% SiO2, 6-14% Al2O3, 0-7.5% B2O3, 0-6.5% MgO, 0-7.1% CaO, 0-15.5% SrO, 1-9.5% BaO and MgO+CaO+SrO+BaO being 16.5- 28%.
5. A flat panel display in accordance with claim 4 in which the glass panel has a CTE in the range of 45-50×10−7/°C. and the aluminosilicate sub-families consist essentially of:
a. 50-57% SiO2, 16-20% Al2O3, 0-5.5% B2O3, 2-2.75% MgO, 1-<7% CaO, 0.5-15% SrO and 1-21% BaO,
b. 55-67% SiO2, 6-<13% Al2O3, 0-7.5% B2O3, 2-6.5% MgO, 0-7.1% CaO, 0-14.5% SrO and 2-9.5% BaO.
6. A flat panel display in accordance with claim 1 in which the glass panel has a strain point greater than 660° C. and a weight loss less than 1 mg/cm2 after immersion for 24 hours in an aqueous 5% by weight HCl solution at 95° C., the glass being selected from a group of aluminosilicate sub-families consisting of glasses having compositions consisting essentially of, as calculated in percent by weight on an oxide basis:
a. 54-58% SiO2, 16-23% Al2O3, 0-6% B2O3, 2-4.5% MgO, 1-7.1% CaO, 2.5-15.5% SrO and 0-14.5% BaO, MgO+CaO+SrO+BaO being 15-27%,
b. 55-67% SiO2, 6-14% Al2O3, 0-7.5% B2O3, 0-7% MgO, 0-7.1% CaO, 0-15% SrO, 1-21% BaO, MgO+CaO+SrO+BaO being 18-28%.
7. A flat panel display in accordance with claim 1 in which the glass panel has a density less than 2.5 grams/cc and a composition, as calculated in weight percent on an oxide basis, consisting essentially of 54.8-57% SiO2, 16.8-21.8% Al2O3, 0 to less than 8% B2O3, 2.2-2.5% MgO, 1.5-7.1% CaO, 4.5-5.5% SrO, 0.1-14.5% BaO, MgO+CaO+SrO+BaO being 12.5-27%.
8. A method of producing a glass panel for a flat panel display which comprises melting a batch for an aluminosilicate glass consisting essentially of, as calculated in percent by weight on an oxide basis, 49-67% SiO2, at least 6% Al2O3, the Al2O3 being 6-14% in conjunction with 55-67% SiO2 and 16-23% in conjunction with 49-58% SiO2, SiO2+Al2O3>68%, 0 to less than 8% B2O3, at least one alkaline earth metal oxide selected from the group consisting of, in the indicated proportions, 0-21% BaO, 0-15% SrO, 0-7.1% CaO, 0-8% MgO and 12-30% BaO+CaO, +SrO+MgO, and drawing a thin sheet of molten glass from the melt.
9. A method in accordance with claim 8 wherein the glass sheet is drawn by a float process.
10. An aluminosilicate glass exhibiting a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5% by weight HCl solution at 95° C., a CTE between 31 and 57×10−7/°C., nominally free of alkali metal oxides and having a composition consisting essentially of, as calculated in percent by weight on an oxide basis, 49-67% SiO2, at least 6% Al2O3, the Al2O3 being 6-14% in conjunction with 55-67% SiO2 and 16-23% in conjunction with 49- 58% SiO2, SiO2+Al2O3>68%, 0 to less than 8% B2O3, at least one alkaline earth metal oxide selected from the group consisting of, in the proportions indicated, 0-21% BaO, 0-15% SrO, 0-7.1% CaO, 0-8% MgO and 12-30% BaO+CaO+SrO+MgO.
11. An aluminosilicate glass in accordance with claim 10 having a CTE in the range of 31-44×10−7/°C. and being selected from a group of aluminosilicate sub-families consisting of glasses having compositions consisting essentially of, as calculated in weight percent on an oxide basis;
a. 49-58% SiO2, 17.5-23% Al2O3, 0 to less than 8% B2O3, 0-8% MgO, 0-7.1% CaO, 0.4-13.5% SrO, 0-21% BaO, the glass containing at least one alkaline earth oxide in the indicated proportion and the total BaO+CaO+SrO+MgO content being 13-28%,
b. 57-66% SiO2, 8-14% Al2O3, 0 to less than 8% B2O3, 0-4.5% MgO, 0-7.1% CaO, 0.5-13% SrO, 2-21% BaO.
12. An aluminosilicate glass in accordance with claim 11 in which the glass has a CTE of 32-40×10−7/°C. and the aluminosilicate sub-families consist essentially of:
a. 54-57% SiO2, 17.5-23% Al2O3, 5 to less than 8% B2O3, 2-2.75% MgO, 1.5-<7% CaO, 2-6% SrO and 0.5-9.5% BaO,
b. 57-65.5% SiO2, 8-13% Al2O3, 4 to less than 8% B2O3, 2-3.5% MgO, 0-6.5% CaO, 0-13% SrO and 2-21% BaO.
13. An aluminosilicate glass in accordance with claim 10 having a CTE in the range of 44-57×10−7/°C. and being selected from a group of aluminosilicate sub-families consisting of glasses having compositions consisting essentially of, as calculated in weight percent on an oxide basis:
a. 50-75% SiO2, 16-22% Al2O3, 0-5.5% B2O3, 0.5-3% MgO, 1-7.1% CaO, 0.5-15% SrO, 1-21% BaO,
b. 55-67% SiO2, 6-14% Al2O3, 0-7.5% B2O3, 0-6.5% MgO, 0-7.1% CaO, 0-15.5% SrO, 1-9.5% BaO, the total MgO+CaO+SrO+BaO being 16.5-28%.
14. An aluminosilicate glass in accordance with claim 13 in which the glass has a CTE in the range of 45-50×10−7/°C. and the aluminosilicate sub-families consist essentially of:
a. 50-57% SiO2, 16-20% Al2O3, 0-5.5% B2O3, 2-2.75% MgO, 1-<7% CaO, 0.5-15% SrO, and 1-21% BaO,
b. 55-67% SiO2, 6-<13% Al2O3, 0-7.5% B2O3, 2-6.5% MgO, 0-7.1% CaO, 0-14.5% SrO and 2-9.5% BaO.
15. An aluminosilicate glass in accordance with claim 10 having a strain point greater than 660° C. and a weight loss less than 1 mg/cm2 after immersion for 24 hours in an aqueous 5% by weight HCl solution at 95° C. and being selected from a group of aluminosilicate sub-families consisting of glasses having compositions consisting essentially of, as calculated in percent by weight on an oxide basis:
a. 54-58% SiO2, 16-23% Al2O3, 0-6% B2O3, 2-4.5% MgO, 1-7.1% CaO, 2.5-15.5% SrO and 0-14.5% BaO, MgO+CaO+SrO+BaO being 15-27%,
b. 55-67% SiO2, 6-14% Al2O3, 0-7.5% B2O3, 0-7% MgO, 0-7.1% CaO, 0-15% SrO, 1-21% BaO, MgO+CaO+SrO+BaO being 18-28%.
16. An aluminosilicate glass in accordance with claim 10 having a density less than 2.5 grams/cc and a composition consisting essentially of 54.8-57% SiO2, 16.8-21.8% Al2O3, 0 to less than 8% B2O3, 2.2-2.5% MgO, 1.5-7.1% CaO, 4.5-5.5% SrO, 0.1-14.5% BaO, MgO+CaO+SrO+BaO being 12.5-27%.
17. An aluminosilicate glass substrate exhibiting a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5% by weight HCl solution at 95° C., a CTE between 31 and 57×10−7/°C., nominally free of alkali metal oxides and having a composition consisting essentially of, as calculated in percent by weight on an oxide basis, 49-67% SiO2, at least 6% Al2O3, the Al2O3 being 6-14% in conjunction with 55-67% SiO2 and 16-23% in conjunction with 49- 58% SiO2, SiO2+Al2O3>68%, 0 to less than 8% B2O3, at least one alkaline earth metal oxide selected from the group consisting of, in the proportions indicated, 0-21% BaO, 0-15% SrO, 0-7.1% CaO, 0-8% MgO and 12-30% BaO+CaO+SrO+MgO.
18. An aluminosilicate glass substrate in accordance with claim 17 having a CTE in the range of 31-44×10−7/°C. and being selected from a group of aluminosilicate sub-families consisting of glasses having compositions consisting essentially of, as calculated in weight percent on an oxide basis;
a. 49-58% SiO2, 17.5-23% Al2O3, 0 to less than 8% B2O3, 0-8% MgO, 0-7.1% CaO, 0.4-13.5% SrO, 0-21% BaO, the glass containing at least one alkaline earth oxide in the indicated proportion and the total BaO+CaO+SrO+MgO content being 13-28%,
b. 57-66% SiO2, 8-14% Al2O3, 0 to less than 8% B2O3, 0-4.5% MgO, 0-7.1% CaO, 0.5-13% SrO, 2-21% BaO.
19. An aluminosilicate glass substrate in accordance with claim 18 in which the glass has a CTE of 32-40×10−7/°C. and the aluminosilicate sub-families consist essentially of:
a. 54-57% SiO2, 17.5-23% Al2O3, 5 to less than 8% B2O3, 2-2.75% MgO, 1.5-<7% CaO, 2-6% SrO and 0.5-9.5% BaO,
b. 57-65.5% SiO2, 8-13% Al2O3, 4 to less than 8% B2O3, 2-3.5% MgO, 0-6.5% CaO, 0-13% SrO and 2-21% BaO.
20. An aluminosilicate glass substrate in accordance with claim 17 having a CTE in the range of 44-57×10−7/°C. and being selected from a group of aluminosilicate sub-families consisting of glasses having compositions consisting essentially of, as calculated in weight percent on an oxide basis:
a. 50-57% SiO2, 16-22% Al2O3, 0-5.5% B2O3, 0.5-3% MgO, 1-7.1% CaO, 0.5-15% SrO, 1-21% BaO,
b. 55-67% SiO2, 6-14% Al2O3, 0-7.5% B2O3, 0-6.5% MgO, 0-7.1% CaO, 0-15.5% SrO, 1-9.5% BaO, the total MgO+CaO+SrO+BaO being 16.5-28%.
21. An aluminosilicate glass substrate in accordance with claim 20 in which the glass has a CTE in the range of 45-50×10−7/°C. and the aluminosilicate sub-families consist essentially of:
a. 50-57% SiO2, 16-20% Al2O3, 0-5.5% B2O3, 2-2.75% MgO, 1-<7% CaO, 0.5-15% SrO and 1-21% BaO,
b. 55-67% SiO2, 6-<13% Al2O3, 0-7.5% B2O3, 2-6.5% MgO, 0-7.1% CaO, 0-14.5% SrO and 2-9.5% BaO.
22. An aluminosilicate glass substrate in accordance with claim 17 having a strain point greater than 660° C. and a weight loss less than 1 mg/cm2 after immersion for 24 hours in an aqueous 5% by weight HCl solution at 95° C. and being selected from a group of aluminosilicate sub-families consisting of glasses having compositions consisting essentially of, as calculated in percent by weight on an oxide basis:
a. 54-58% SiO2, 16-23% Al2O3, 0-6% B2O3, 2-4.5% MgO, 1-7.1% CaO, 2.5-15.5% SrO and 0-14.5% BaO, MgO+CaO+SrO+BaO being 15-27%,
b. 55-67% SiO2, 6-14% Al2O3, 0-7.5% B2O3, 0-7% MgO, 0-7.1% CaO, 0-15% SrO, 1-21% BaO, MgO+CaO+SrO+BaO being 18-28%.
23. An aluminosilicate glass substrate in accordance with claim 17 having a density less than 2.5 grams/cc and a composition consisting essentially of 54.8-57% SiO2, 16.8-21.8% Al2O3, 0 to less than 8% B2O3, 2.2-2.5% MgO, 1.5-7.1% CaO, 4.5-5.5% SrO, 0.1-14.5% BaO, MgO+CaO+SrO+BaO being 12.5-27%.
24. A method of producing a glass panel for a flat panel display, by a float glass process, which comprises melting a batch for an aluminosilicate glass consisting essentially of, as calculated in percent by weight on an oxide basis, 60 up to 67% SiO 2 , at least 6 % Al 2 O 3 , SiO 2 +Al 2 O 3 >68 %, B 2 O 3 which is present in an amount of up to 8 %, at least one alkaline earth metal oxide selected from the group consisting of, in the proportions indicated, 0-21 % BaO, 0-15 % SrO, 0-7.1 % CaO, 0-8 % MgO and 12-30 % BaO+CaO+SrO+MgO and drawing a thin sheet of molten glass from the melt.
25. A method according to claim 24, wherein the aluminosilicate glass composition consists essentially of above 60 up to 67% SiO 2 .
26. A method of producing a glass panel for a flat panel display which comprises melting a batch for an aluminosilicate glass consisting essentially of, as calculated in weight percent on an oxide basis, above 60% up to 67 % SiO 2 , at least 6 % Al 2 O 3 , SiO 2 +Al 2 O 3 >68 %, B 2 O 3 which is present in an amount of up to 15 %, at least one alkaline earth metal oxide selected from the group consisting of, in the proportions indicated, 0-21 % BaO, 0-15 % SrO, 0-7.1 % CaO, 0-8 % MgO and 12-30 % BaO+CaO+SrO+MgO, and drawing a thin sheet of molten glass from the melt by a float process.
27. A method of producing a glass panel for a flat panel display which comprises melting a batch for aluminosilicate glass which is nominally free of alkali metal oxides and has a composition that consists essentially of, as calculated in percent by weight on an oxide basis, 49-58% SiO 2 , 17.5-23 % Al 2 O 3 , 0-14.5 % B 2 O 3 , 0-8 % MgO, 0-9 % CaO, 0.4-13.5 % SrO, 0-21 % BaO, and 13-28 % MgO+CaO+SrO+BaO, and drawing a thin sheet of molten glass from the melt by a float process wherein the glass panel has a strain point higher than 640° C., a CTE in the range of 31-44×10 −7 /° C., and a weight loss less than 2.5 mg/cm 2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C.
28. The method according to claim 27, wherein the CTE is in the range of 32-40×10 −7 /° C.
29. The method according to claim 27, wherein the glass panel has a CTE in the range of 32-40×10 −7 /° C. and the glass has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, 54-57 % SiO 2 , 17.5-23 % Al 2 O 3 , 5 to less than 8 % B 2 O 3 , 2-2.75 % MgO, 1.5-<7 % CaO, 2-6 % SrO, and 0.5-9.5 % BaO.
30. A glass panel produced by the method of claim 27.
31. A flat panel display comprising an aluminosilicate glass panel that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 31-44×10 −7 /° C., is nominally free of alkali metal oxides, and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, 57-66 % SiO 2 , 8-14 % Al 2 O 3 , 0 to less than 8 % B 2 O 3 , 0-4.5 % MgO, 0-7.1 % CaO, 0.5-13 % SrO, and 2-21 % BaO.
32. A flat panel display comprising an aluminosilicate glass panel that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 32-40×10 −7 /° C., is nominally free of alkali metal oxides, and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, either:
a. 54-57 % SiO 2 , 17.5-23 % Al 2 O 3 , 5 to less than 8 % B 2 O 3 , 2-2.75 % MgO, 1.5-<7.1 % CaO, 2-6 % SrO, and 0.5-9.5 % BaO or
b. 57-65.5 % SiO 2 , 8-13 % Al 2 O 3 , 4 to less than 8 % B 2 O 3 , 2-3.5 % MgO, 0-6.5 % CaO, 0-13 % SrO, and 2-21 % BaO.
33. A flat panel display comprising an aluminosilicate glass panel that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 44-57×10 −7 /° C., is nominally free of alkali metal oxides and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, either:
a. 50-57 % SiO 2 , 16-22 % Al 2 O 3 , 0-5.5 % B 2 O 3 , 0.5-3 % MgO, 1-7.1 % CaO, 0.5-15 % SrO, and 1-21 % BaO or
b. 55-67 % SiO 2 , 6-14 % Al 2 O 3 , 0-7.5 % B 2 O 3 , 0-6.5 % MgO, 0-7.1 % CaO, 0-15.5 % SrO, 1-9.5 % BaO, and MgO+CaO+SrO+BaO being 16.5-28 %.
34. A flat panel display comprising an aluminosilicate glass panel that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 45-50×10 −7 /° C., is nominally free of alkali metal oxides and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, either:
a. 50-57 % SiO 2 , 16-20 % Al 2 O 3 , 0-5.5 % B 2 O 3 , 2-2.75 % MgO, 1-<7 % CaO, 0.5-15 % SrO, and 1-21 % BaO or
b. 55-67 % SiO 2 , 6-<13 % Al 2 O 3 , 0-7.5 % B 2 O 3 , 2-6.5 % MgO, 0-7.1 % CaO, 0-14.5 % SrO, and 2-9.5 % BaO.
35. A flat panel display comprising an aluminosilicate glass panel that exhibits a strain point higher than 660° C., a weight loss less than 1 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 31-57×10 −7 /° C., is nominally free of alkali metal oxides and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, either:
a. 54-58 % SiO 2 , 16-23 % Al 2 O 3 , 0-6 % B 2 O 3 , 2-4.5 % MgO, 1-7.1 % CaO, 2.5-15.5 % SrO, and 0-14.5 % BaO, MgO+CaO+SrO+BaO being 15-27 % or
b. 55-67 % SiO 2 , 6-14 % Al 2 O 3 , 0-7.5 % B 2 O 3 , 0-7 % MgO, 0-7.1 % CaO, 0-15 % SrO, 1-21 % BaO, and MgO+CaO+SrO+BaO being 18-28 %.
36. A flat panel display comprising an aluminosilicate glass panel that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 31-57×10 −7 /° C., is nominally free of alkali metal oxides, has a density less than 2.5 grams/cc, and a composition consisting essentially of, as calculated in percent by weight on an oxide basis, 54.8-57 % SiO 2 , 16.8-21.8 % Al 2 O 3 , 0 to less than 8 % B 2 O 3 , 2.2-2.5 % MgO, 1.5-7.1 % CaO, 4.5-5.5 % SrO, 0.1-14.5 % BaO, and MgO+CaO+SrO+BaO being 12.5-27 %.
37. An aluminosilicate glass that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 31-44×10 −7 /° C., is nominally free of alkali metal oxides, and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, 57-66 % SiO 2 , 8-14 % Al 2 O 3 , 0 to less than 8 % B 2 O 3 , 0-4.5 % MgO, 0-7.1 % CaO, 0.5-13 % SrO, and 2-21 % BaO.
38. An aluminosilicate glass that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 32-40×10 −7 /° C., is nominally free of alkali metal oxides, and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, either:
a. 54-57 % SiO 2 , 17.5-23 % Al 2 O 3 , 5 to less than 8 % B 2 O 3 , 2-2.75 % MgO, 1.5-<7 % CaO, 2-6 % SrO, and 0.5-9.5 % BaO or
b. 57-65.5 % SiO 2 , 8-13 % Al 2 O 3 , 4 to less than 8 % B 2 O 3 , 2-3.5 % MgO, 0-6.5 % CaO, 0-13 % SrO, and 2-21 % BaO.
39. An aluminosilicate glass that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 44-57×10 −7 /° C., is nominally free of alkali metal oxides, and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, either:
a. 50-57 % SiO 2 , 16-22 % Al 2 O 3 , 0-5.5 % B 2 O 3 , 0.5-3 % MgO, 1-7.1 % CaO, 0.5-15 % SrO, and 1-21 % BaO or
b. 55-67 % SiO 2 , 6-14 % Al 2 O 3 , 0-7.5 % B 2 O 3 , 0-6.5 % MgO, 0-7.1 % CaO, 0-15.5 % SrO, 1-9.5 % BaO, and the total MgO+CaO+SrO+BaO being 16.5-28 %.
40. An aluminosilicate glass that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 45-50×10 −7 /° C., is nominally free of alkali metal oxides, and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, either:
a. 50-57 % SiO 2 , 16-20 % Al 2 O 3 , 0-5.5 % B 2 O 3 , 2-2.75 % MgO, 1-<7 % CaO, 0.5-15 % SrO, and 1-21 % BaO or
b. 55-67 % SiO 2 , 6-<13 % Al 2 O 3 , 0-7.5 % B 2 O 3 , 2-6.5 % MgO, 0-7.1 % CaO, 0-14.5 % SrO, and 2-9.5 % BaO.
41. An aluminosilicate glass that exhibits a strain point higher than 660° C., a weight loss less than 1 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 31-57×10 −7 /° C., is nominally free of alkali metal oxides and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, either:
a. 54-58 % SiO 2 , 16-23 % Al 2 O 3 , 0-6 % B 2 O 3 , 2-4.5 % MgO, 1-7.1 % CaO, 2.5-15.5 % SrO, 0-14.5 % BaO, and MgO+CaO+SrO+BaO being 15-27 % or
b. 55-67 % SiO 2 , 6-14 % Al 2 O 3 , 0-7.5 % B 2 O 3 , 0-7 % MgO, 0-7.1 % CaO, 0-15 % SrO, 1-21 % BaO, and MgO+CaO+SrO+BaO being 18-28 %.
42. An aluminosilicate glass that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 31-57×10 −7 /° C., is nominally free of alkali metal oxides, has a density less than 2.5 grams/cc, and a composition consisting essentially of, as calculated in percent by weight on an oxide basis, 54.8-57 % SiO 2 , 16.8-21.8 % Al 2 O 3 , 0 to less than 8 % B 2 O 3 , 2.2-2.5 % MgO, 1.5-7.1 % CaO, 4.5-5.5 % SrO, 0.1-14.5 % BaO, and MgO+CaO+SrO+BaO being 12.5-27 %.
43. An aluminosilicate glass that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 31-44×10 −7 /° C., is nominally free of alkali metal oxides, and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, 57-66 % SiO 2 , 8-14 % Al 2 O 3 , 0 to less than 8 % B 2 O 3 , 0-4.5 % MgO, 0-7.1 % CaO, 0.5-13 % SrO, and 2-21 % BaO.
44. A aluminosilicate glass that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 32-40×10 −7 /° C., is nominally free of alkali metal oxides, and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, either:
a. 54-57 % SiO 2 , 17.5-23 % Al 2 O 3 , 5 to less than 8 % B 2 O 3 , 2-2.75 % MgO, 1.5-<7 % CaO, 2-6 % SrO, and 0.5-9.5 % BaO or
b. 57-65.5 % SiO 2 , 8-13 % Al 2 O 3 , 4 to less than 8 % B 2 O 3 , 2-3.5 % MgO, 0-6.5 % CaO, 0-13 % SrO, and 2-21 % BaO.
45. An aluminosilicate glass that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 44-57×10 −7 /° C., is nominally free of alkali metal oxides, and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, either:
a. 50-57 % SiO 2 , 16-22 % Al 2 O 3 , 0-5.5 % B 2 O 3 , 0.5-3 % MgO, 1-7.1 % CaO, 0.5-15 % SrO, and 1-21 % BaO or
b. 55-67 % SiO 2 , 6-14 % Al 2 O 3 , 0-7.5 % B 2 O 3 , 0-6.5 % MgO, 0-7.1 % CaO, 0-15.5 % SrO, 1-9.5 % BaO, and the total MgO+CaO+SrO+BaO being 16.5-28 %.
46. An aluminosilicate glass that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 45-50×10 −7 /° C., is nominally free of alkali metal oxides, and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, either:
a. 50-57 % SiO 2 , 16-20 % Al 2 O 3 , 0-5.5 % B 2 O 3 , 2-2.75 % MgO, 1-<7 % CaO, 0.5-15 % SrO, and 1-21 % BaO or
b. 55-67 % SiO 2 , 6-<13 % Al 2 O 3 , 0-7.5 % B 2 O 3 , 2-6.5 % MgO, 0-7.1 % CaO, 0-14.5 % SrO, and 2-9.5 % BaO.
47. An aluminosilicate glass panel that exhibits a strain point higher than 660° C., a weight loss less than 1 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 31-57×10 −7 /° C., is nominally free of alkali metal oxides and has a composition consisting essentially of, as calculated in percent by weight on an oxide basis, either:
a. 54-58 % SiO 2 , 16-23 % Al 2 O 3 , 0-6 % B 2 O 3 , 2-4.5 % MgO, 1-7.1 % CaO, 2.5-15.5 % SrO, 0-14.5 % BaO, and MgO+CaO+SrO+BaO being 15-27 % or
b. 55-67 % SiO 2 , 6-14 % Al 2 O 3 , 0-7.5 % B 2 O 3 , 0-7 % MgO, 0-7.1 % CaO, 0-15 % SrO, 1-21 % BaO, and MgO+CaO+SrO+BaO being 18-28 %.
48. An aluminosilicate glass panel that exhibits a strain point higher than 640° C., a weight loss less than 2.5 mg/cm2 after immersion for 24 hours in an aqueous 5 % by weight HCl solution at 95° C., a CTE in the range of 31-57×10 −7 /° C., is nominally free of alkali metal oxides, has a density less than 2.5 grams/cc, and a composition consisting essentially of, as calculated in percent by weight on an oxide basis, 54.8-57 % SiO 2 , 16.8-21.8 % Al 2 O 3 , 0 to less than 8 % B 2 O 3 , 2.2-2.5 % MgO, 1.5-7.1 % CaO, 4.5-5.5 % SrO, 0.1-14.5 % BaO, and MgO+CaO+SrO+BaO being 12.5-27 %.
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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040127342A1 (en) * 2002-12-27 2004-07-01 China Optoelectronics Technology Corp. Glass composition of a substrate for display
US20050028559A1 (en) * 2002-02-15 2005-02-10 Asahi Glass Company Limited Process for producing float glass
US20060003884A1 (en) * 2003-03-31 2006-01-05 Asahi Glass Company, Limited Alkali free glass
US20060083474A1 (en) * 2002-01-22 2006-04-20 Color Chip (Israel) Ltd. Potassium free zinc silicate glasses for ion-exchange processes
US20060127679A1 (en) * 2004-12-13 2006-06-15 Gulati Suresh T Glass laminate substrate having enhanced impact and static loading resistance
US20070112123A1 (en) * 2005-11-11 2007-05-17 Asahi Fiber Glass Company, Limited Glass filler for polycarbonate resin, and polycarbonate resin composition
US20070191207A1 (en) * 2006-02-10 2007-08-16 Danielson Paul S Glass compositions having high thermal and chemical stability and methods of making thereof
US20110201490A1 (en) * 2009-08-21 2011-08-18 Barefoot Kristen L Crack and scratch resistant glass and enclosures made therefrom
US8975199B2 (en) * 2011-08-12 2015-03-10 Corsam Technologies Llc Fusion formable alkali-free intermediate thermal expansion coefficient glass
WO2016018861A1 (en) 2014-07-30 2016-02-04 Corning Incorporated High contrast, glass-based, writeable/erasable front projection screens
US9309139B2 (en) 2013-02-15 2016-04-12 Corning Incorporated High volume production of display quality glass sheets having low zirconia levels
US9370902B2 (en) 2013-10-03 2016-06-21 Comerstone Research Group, Inc. Fiber-reinforced epoxy composites and methods of making same without the use of oven or autoclave
US9670088B2 (en) 2014-05-20 2017-06-06 Corning Incorporated Scratch resistant glass and method of making
US10167379B1 (en) 2014-10-06 2019-01-01 Cornerstone Research Group, Inc. Hybrid fiber layup and fiber-reinforced polymeric composites produced therefrom
US10946594B1 (en) 2017-01-06 2021-03-16 Cornerstone Research Group, Inc. Reinforced polymer-infused fiber composite repair system and methods for repairing composite materials

Families Citing this family (85)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5508237A (en) 1994-03-14 1996-04-16 Corning Incorporated Flat panel display
FR2727399B1 (en) * 1994-10-13 1997-01-31 Saint Gobain Vitrage SILICO-SODO-CALCIUM GLASS COMPOSITIONS AND THEIR APPLICATIONS
JPH09507206A (en) * 1994-10-13 1997-07-22 サン−ゴバン ビトラージュ ソシエテ アノニム Tempered glass base material
US5599754A (en) * 1994-10-14 1997-02-04 Asahi Glass Company Ltd. Glass composition for a substrate, and substrate for plasma display made thereof
DE69508706T2 (en) * 1994-11-30 1999-12-02 Asahi Glass Co Ltd Alkali-free glass and flat screen
US5741746A (en) * 1995-03-02 1998-04-21 Kohli; Jeffrey T. Glasses for display panels
US5885914A (en) * 1995-07-28 1999-03-23 Asahi Glass Company Ltd. Alkali-free glass and display substrate
WO1997011920A1 (en) * 1995-09-28 1997-04-03 Nippon Electric Glass Co., Ltd. Alkali-free glass substrate
US5786286A (en) * 1995-10-31 1998-07-28 Corning Incorporated Glass ceramic rear panel for emissive display
DE19603698C1 (en) * 1996-02-02 1997-08-28 Schott Glaswerke Alkali-free aluminoborosilicate glass and its use
JP3800657B2 (en) * 1996-03-28 2006-07-26 旭硝子株式会社 Alkali-free glass and flat display panel
DE19617344C1 (en) * 1996-04-30 1997-08-07 Schott Glaswerke Alkali-free alumino:borosilicate glass
US5824127A (en) * 1996-07-19 1998-10-20 Corning Incorporated Arsenic-free glasses
US6060168A (en) * 1996-12-17 2000-05-09 Corning Incorporated Glasses for display panels and photovoltaic devices
DE19739912C1 (en) * 1997-09-11 1998-12-10 Schott Glas New alkali-free aluminoborosilicate glass
DE19747355C1 (en) * 1997-10-27 1999-06-24 Schott Glas Long-life halogen cycle lamp operating at above 85 volts
EP2374765A1 (en) * 1997-09-12 2011-10-12 Schott Ag Long life halogen cycle incandescent lamp and glass envelope compoistion
DE19758481C1 (en) * 1997-10-27 1999-06-17 Schott Glas Glass with high thermal resistance for lamp bulbs and their use
US6069100A (en) * 1997-10-27 2000-05-30 Schott Glas Glass for lamb bulbs capable of withstanding high temperatures
DE19747354C1 (en) * 1997-10-27 1998-12-24 Schott Glas New cerium oxide-containing alkaline earth aluminoborosilicate glass
US5854152A (en) * 1997-12-10 1998-12-29 Corning Incorporated Glasses for display panels
DE19840113B9 (en) * 1998-09-03 2016-10-13 Eglass Asia Ltd. Alkali-free glass composition for the production of flat glass
DE19851927C2 (en) * 1998-11-11 2001-02-22 Schott Glas Thermally resistant glass and its use
JP4547093B2 (en) * 1998-11-30 2010-09-22 コーニング インコーポレイテッド Glass for flat panel display
DE19916296C1 (en) * 1999-04-12 2001-01-18 Schott Glas Alkali-free aluminoborosilicate glass and its use
JP2001013488A (en) * 1999-06-29 2001-01-19 Asahi Glass Co Ltd Liquid crystal display
DE19934072C2 (en) * 1999-07-23 2001-06-13 Schott Glas Alkali-free aluminoborosilicate glass, its uses and processes for its manufacture
US6537937B1 (en) * 1999-08-03 2003-03-25 Asahi Glass Company, Limited Alkali-free glass
DE19939789A1 (en) * 1999-08-21 2001-02-22 Schott Glas Alkali-free aluminoborosilicate glasses and their uses
US6071839A (en) * 1999-08-26 2000-06-06 Corning Inc. Colorant glasses
DE19942259C1 (en) 1999-09-04 2001-05-17 Schott Glas Alkaline earth aluminum borosilicate glass and its uses
DE19959084B4 (en) * 1999-12-08 2005-05-12 Schott Ag Organic LED display and process for its manufacture
DE10000836B4 (en) * 2000-01-12 2005-03-17 Schott Ag Alkali-free aluminoborosilicate glass and its uses
DE10000839C1 (en) * 2000-01-12 2001-05-10 Schott Glas Alkali-free aluminoborosilicate glass used as substrate glass in displays and in thin layer photovoltaics contains oxides of silicon, boron, aluminum, magnesium, calcium, strontium, barium and zinc
DE10000837C1 (en) * 2000-01-12 2001-05-31 Schott Glas Alkali-free alumino-borosilicate glass used as substrate glass in thin film transistor displays and thin layer solar cells contains oxides of silicon, boron, aluminum, magnesium, strontium, and barium
DE10000838B4 (en) 2000-01-12 2005-03-17 Schott Ag Alkali-free aluminoborosilicate glass and its uses
DE10006305C2 (en) * 2000-02-12 2002-08-01 Schott Rohrglas Gmbh Glass with high thermal resistance for lamp bulbs and its use
US7211957B2 (en) * 2000-05-05 2007-05-01 Telux-Spezialglas Gmbh Alumino earth-alkali silicate glasses with high thermal capacity for light bulbs and use thereof
DE10034985C1 (en) * 2000-07-19 2001-09-06 Schott Glas Production of an alkali-free aluminosilicate glass used as a substrate glass for displays comprises adding tin oxide as refining agent to the starting materials, melting the glass and hot molding the glass
DE10064804C2 (en) * 2000-12-22 2003-03-20 Schott Glas Alkali-free aluminoborosilicate glasses and their use
DE10114581C2 (en) * 2001-03-24 2003-03-27 Schott Glas Alkali-free aluminoborosilicate glass and uses
JP2002350816A (en) * 2001-05-28 2002-12-04 Matsushita Electric Ind Co Ltd Liquid crystal display device and its manufacturing method
US6753279B2 (en) 2001-10-30 2004-06-22 Corning Incorporated Glass composition for display panels
TWI318198B (en) * 2002-03-11 2009-12-11 Tosoh Corp Highly durable silica glass, process for producing same, member comprised thereof, and apparatus provided therewith
CA2412379A1 (en) * 2002-11-22 2004-05-22 Luxell Technolgies Inc. Transparent-cathode for top-emission organic light-emitting diodes
EP1705160A4 (en) * 2003-12-26 2009-05-06 Asahi Glass Co Ltd No alkali glass, method for production thereof and liquid crystalline display panel
DE102004007436B4 (en) * 2004-02-16 2017-11-16 Schott Ag Use of a B2O3-free crystallization-stable aluminosilicate glass and its preparation
CN102219355B (en) * 2005-12-16 2013-05-22 日本电气硝子株式会社 Non-alkali glass substrate and method for producing same
US8007913B2 (en) * 2006-02-10 2011-08-30 Corning Incorporated Laminated glass articles and methods of making thereof
DE102006016256B4 (en) * 2006-03-31 2013-12-12 Schott Ag Aluminoborosilicate glass and its use
CN101484838B (en) 2006-06-30 2011-11-02 旭硝子株式会社 Liquid crystal display panel
JP5071878B2 (en) * 2006-09-12 2012-11-14 日本電気硝子株式会社 Alkali-free glass and alkali-free glass substrate using the same
DE102008005857A1 (en) 2008-01-17 2009-07-23 Schott Ag Alkali-free glass
RU2010154445A (en) 2008-05-30 2012-07-10 Фостер Вилер Энергия Ой (Fi) METHOD AND SYSTEM FOR ENERGY GENERATION BY BURNING IN PURE OXYGEN
CN101337770B (en) * 2008-08-18 2011-06-22 苏州新吴硝子科技有限公司 High strength aluminosilicate glass and chemically toughening process thereof
US8051679B2 (en) * 2008-09-29 2011-11-08 Corning Incorporated Laser separation of glass sheets
US8713967B2 (en) * 2008-11-21 2014-05-06 Corning Incorporated Stable glass sheet and method for making same
CN102471134B (en) 2009-07-02 2015-04-15 旭硝子株式会社 Alkali-free glass and method for producing same
TWI418526B (en) * 2009-07-08 2013-12-11 Nippon Electric Glass Co Glass plate
JP5642363B2 (en) * 2009-08-14 2014-12-17 日本板硝子株式会社 Glass substrate
DE102009051852B4 (en) 2009-10-28 2013-03-21 Schott Ag Borless glass and its use
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JP5751439B2 (en) * 2010-08-17 2015-07-22 日本電気硝子株式会社 Alkali-free glass
CN102030461B (en) * 2010-10-13 2012-08-15 中国科学院理化技术研究所 Method for preparing rare earth aluminum silicate glass
WO2012063643A1 (en) * 2010-11-08 2012-05-18 日本電気硝子株式会社 Alkali-free glass
DE102010054967B4 (en) 2010-12-08 2014-08-28 Schott Ag Boreless universal glass and its use
KR101751569B1 (en) 2010-12-27 2017-06-27 아사히 가라스 가부시키가이샤 Non-alkali glass, and process for production of non-alkali glass
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JP6032014B2 (en) * 2012-04-24 2016-11-24 日本電気硝子株式会社 Crystalline glass composition
US9034442B2 (en) * 2012-11-30 2015-05-19 Corning Incorporated Strengthened borosilicate glass containers with improved damage tolerance
JP6256744B2 (en) * 2013-10-17 2018-01-10 日本電気硝子株式会社 Alkali-free glass plate
JP6323139B2 (en) * 2014-04-17 2018-05-16 旭硝子株式会社 Glass for pharmaceutical or cosmetic containers
US20170226000A1 (en) * 2014-08-13 2017-08-10 Corning Incorporated Intermediate cte glasses and glass articles comprising the same
JP5988059B2 (en) * 2014-11-06 2016-09-07 日本電気硝子株式会社 Alkali-free glass
CN107207322A (en) 2015-04-03 2017-09-26 日本电气硝子株式会社 Glass
US20180319700A1 (en) * 2015-12-01 2018-11-08 Kornerstone Materials Technology Company, Ltd. Low-boron, barium-free, alkaline earth aluminosilicate glass and its applications
CN109071317A (en) * 2016-04-27 2018-12-21 Agc株式会社 alkali-free glass
WO2018116731A1 (en) * 2016-12-19 2018-06-28 日本電気硝子株式会社 Glass
JP6955522B2 (en) * 2018-01-17 2021-10-27 日本電気硝子株式会社 Glass and glass substrate
JP6770984B2 (en) * 2018-01-17 2020-10-21 日本電気硝子株式会社 Glass and glass substrate
JP6709519B2 (en) * 2019-01-31 2020-06-17 日本電気硝子株式会社 Glass and glass substrate
CN110240405B (en) * 2019-06-26 2022-05-17 鲁米星特种玻璃科技股份有限公司 Alkali-resistant aluminosilicate glass and application thereof
CN115784616A (en) * 2022-11-15 2023-03-14 常熟佳合显示科技有限公司 MAS microcrystalline glass and preparation method thereof

Citations (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3496401A (en) 1965-12-30 1970-02-17 Corning Glass Works Glass envelopes for iodine cycle incandescent lamps
US3978362A (en) 1975-08-07 1976-08-31 Corning Glass Works Glass envelope for tungsten-bromine lamp
US4012263A (en) 1975-02-10 1977-03-15 Owens-Illinois, Inc. Alkali-free glasses
US4060423A (en) 1976-07-27 1977-11-29 General Electric Company High-temperature glass composition
US4180618A (en) 1977-07-27 1979-12-25 Corning Glass Works Thin silicon film electronic device
US4255198A (en) 1979-11-09 1981-03-10 Corning Glass Works Glass for sealing to molybdenum metal
US4302250A (en) 1980-09-08 1981-11-24 Corning Glasss Works Glass envelopes for tungsten-halogen lamps
US4394453A (en) 1981-09-08 1983-07-19 Corning Glass Works Envelopes for tungsten-halogen lamps
US4409337A (en) 1982-11-12 1983-10-11 Corning Glass Works Glass envelopes for tungsten-halogen lamps
US4441051A (en) 1982-02-22 1984-04-03 General Electric Company Lamp seal glass
US4634683A (en) 1985-10-23 1987-01-06 Corning Glass Works Barium and/or strontium aluminosilicate crystal-containing glasses for flat panel display devices
US4634684A (en) 1985-10-23 1987-01-06 Corning Glass Works Strontium aluminosilicate glass substrates for flat panel display devices
JPS627874A (en) 1985-06-20 1987-01-14 ヘンケル・コマンデイツトゲゼルシヤフト・アウフ・アクチエン Aqueous composition for flux and highlight method and its use
JPS63221315A (en) 1987-03-11 1988-09-14 Ricoh Co Ltd Polygonal scanner motor
JPS63283710A (en) 1987-05-18 1988-11-21 Takara Kogyo Kk Filter
US4824808A (en) 1987-11-09 1989-04-25 Corning Glass Works Substrate glass for liquid crystal displays
US4994415A (en) 1986-09-17 1991-02-19 Nippon Electric Glass Company, Limited SiO2 -Al2 O3 -BaO glass substrates with improved chemical resistance for use in display panels and others having thin films
JPH0416003A (en) 1990-05-10 1992-01-21 Toshiba Corp Voltage controlled oscillator
US5116787A (en) 1991-08-12 1992-05-26 Corning Incorporated High alumina, alkaline earth borosilicate glasses for flat panel displays
US5116788A (en) 1991-08-12 1992-05-26 Corning Incorporated Alkaline earth aluminoborosilicate glasses for flat panel displays
US5116789A (en) 1991-08-12 1992-05-26 Corning Incorporated Strontium aluminosilicate glasses for flat panel displays
JPH04175242A (en) 1990-11-06 1992-06-23 Asahi Glass Co Ltd Non-alkali glass
FR2675795A1 (en) 1991-04-26 1992-10-30 Nippon Sheet Glass Co Ltd NON ALKALINE GLASS.
EP0559389A2 (en) 1992-03-03 1993-09-08 Pilkington Plc Alkali-free glass compositions
US5348916A (en) 1991-04-26 1994-09-20 Asahi Glass Company Ltd. Alkali free glass
US5374595A (en) 1993-01-22 1994-12-20 Corning Incorporated High liquidus viscosity glasses for flat panel displays
US5387560A (en) 1991-07-02 1995-02-07 Saint Gobain Vitrage International Glasses for substrates intended for electronics and resultant products
EP0672629A2 (en) 1994-03-14 1995-09-20 Corning Incorporated Aluminosilicate glass for flat panel display
US5489558A (en) 1994-03-14 1996-02-06 Corning Incorporated Glasses for flat panel display

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61236631A (en) * 1985-04-10 1986-10-21 Ohara Inc Refractory and heat resistant glass
JPS61261232A (en) * 1985-05-13 1986-11-19 Ohara Inc Fire-resistant and heat-resistant glass
JPS61295256A (en) * 1985-06-21 1986-12-26 Ohara Inc Glass for substrate
JPS63133334A (en) * 1986-11-21 1988-06-06 Sanyo Electric Co Ltd Manufacture of master disk for optical disk
JPH0825772B2 (en) * 1987-01-16 1996-03-13 日本板硝子株式会社 Glass for electronic device substrates
JP2707625B2 (en) * 1987-10-01 1998-02-04 旭硝子株式会社 Alkali-free glass for display substrates
JPH0624998B2 (en) * 1988-11-11 1994-04-06 セントラル硝子株式会社 Alkali free glass
JP2644622B2 (en) * 1990-10-24 1997-08-25 ホーヤ株式会社 Glass for liquid crystal display substrates
JP3083586B2 (en) * 1991-04-26 2000-09-04 旭硝子株式会社 Alkali-free glass

Patent Citations (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3496401A (en) 1965-12-30 1970-02-17 Corning Glass Works Glass envelopes for iodine cycle incandescent lamps
US4012263A (en) 1975-02-10 1977-03-15 Owens-Illinois, Inc. Alkali-free glasses
US3978362A (en) 1975-08-07 1976-08-31 Corning Glass Works Glass envelope for tungsten-bromine lamp
US4060423A (en) 1976-07-27 1977-11-29 General Electric Company High-temperature glass composition
US4180618A (en) 1977-07-27 1979-12-25 Corning Glass Works Thin silicon film electronic device
US4255198A (en) 1979-11-09 1981-03-10 Corning Glass Works Glass for sealing to molybdenum metal
US4302250A (en) 1980-09-08 1981-11-24 Corning Glasss Works Glass envelopes for tungsten-halogen lamps
US4394453A (en) 1981-09-08 1983-07-19 Corning Glass Works Envelopes for tungsten-halogen lamps
US4441051A (en) 1982-02-22 1984-04-03 General Electric Company Lamp seal glass
US4409337A (en) 1982-11-12 1983-10-11 Corning Glass Works Glass envelopes for tungsten-halogen lamps
JPS627874A (en) 1985-06-20 1987-01-14 ヘンケル・コマンデイツトゲゼルシヤフト・アウフ・アクチエン Aqueous composition for flux and highlight method and its use
US4634683A (en) 1985-10-23 1987-01-06 Corning Glass Works Barium and/or strontium aluminosilicate crystal-containing glasses for flat panel display devices
US4634684A (en) 1985-10-23 1987-01-06 Corning Glass Works Strontium aluminosilicate glass substrates for flat panel display devices
US4994415A (en) 1986-09-17 1991-02-19 Nippon Electric Glass Company, Limited SiO2 -Al2 O3 -BaO glass substrates with improved chemical resistance for use in display panels and others having thin films
JPS63221315A (en) 1987-03-11 1988-09-14 Ricoh Co Ltd Polygonal scanner motor
JPS63283710A (en) 1987-05-18 1988-11-21 Takara Kogyo Kk Filter
US4824808A (en) 1987-11-09 1989-04-25 Corning Glass Works Substrate glass for liquid crystal displays
JPH0416003A (en) 1990-05-10 1992-01-21 Toshiba Corp Voltage controlled oscillator
JPH04175242A (en) 1990-11-06 1992-06-23 Asahi Glass Co Ltd Non-alkali glass
FR2675795A1 (en) 1991-04-26 1992-10-30 Nippon Sheet Glass Co Ltd NON ALKALINE GLASS.
US5348916A (en) 1991-04-26 1994-09-20 Asahi Glass Company Ltd. Alkali free glass
US5387560A (en) 1991-07-02 1995-02-07 Saint Gobain Vitrage International Glasses for substrates intended for electronics and resultant products
US5116788A (en) 1991-08-12 1992-05-26 Corning Incorporated Alkaline earth aluminoborosilicate glasses for flat panel displays
US5116789A (en) 1991-08-12 1992-05-26 Corning Incorporated Strontium aluminosilicate glasses for flat panel displays
US5116787A (en) 1991-08-12 1992-05-26 Corning Incorporated High alumina, alkaline earth borosilicate glasses for flat panel displays
EP0559389A2 (en) 1992-03-03 1993-09-08 Pilkington Plc Alkali-free glass compositions
US5374595A (en) 1993-01-22 1994-12-20 Corning Incorporated High liquidus viscosity glasses for flat panel displays
EP0672629A2 (en) 1994-03-14 1995-09-20 Corning Incorporated Aluminosilicate glass for flat panel display
US5489558A (en) 1994-03-14 1996-02-06 Corning Incorporated Glasses for flat panel display

Cited By (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060083474A1 (en) * 2002-01-22 2006-04-20 Color Chip (Israel) Ltd. Potassium free zinc silicate glasses for ion-exchange processes
US20050028559A1 (en) * 2002-02-15 2005-02-10 Asahi Glass Company Limited Process for producing float glass
US20040127342A1 (en) * 2002-12-27 2004-07-01 China Optoelectronics Technology Corp. Glass composition of a substrate for display
US20060003884A1 (en) * 2003-03-31 2006-01-05 Asahi Glass Company, Limited Alkali free glass
US20060127679A1 (en) * 2004-12-13 2006-06-15 Gulati Suresh T Glass laminate substrate having enhanced impact and static loading resistance
US7201965B2 (en) 2004-12-13 2007-04-10 Corning Incorporated Glass laminate substrate having enhanced impact and static loading resistance
US7700682B2 (en) * 2005-11-11 2010-04-20 Asahi Fiber Glass Company, Limited Glass filler for polycarbonate resin, and polycarbonate resin composition
US20070112123A1 (en) * 2005-11-11 2007-05-17 Asahi Fiber Glass Company, Limited Glass filler for polycarbonate resin, and polycarbonate resin composition
US8753993B2 (en) * 2006-02-10 2014-06-17 Corning Incorporated Glass compositions having high thermal and chemical stability and methods of making thereof
US10364177B2 (en) 2006-02-10 2019-07-30 Corning Incorporated Glass compositions having high thermal and chemical stability and methods of making thereof
US20110048074A1 (en) * 2006-02-10 2011-03-03 Danielson Paul S Glass compositions having high thermal and chemical stability and methods of making thereof
US7833919B2 (en) * 2006-02-10 2010-11-16 Corning Incorporated Glass compositions having high thermal and chemical stability and methods of making thereof
US20130065747A1 (en) * 2006-02-10 2013-03-14 Paul Stephen Danielson Glass compositions having high thermal and chemical stability and methods of making thereof
US8763429B2 (en) * 2006-02-10 2014-07-01 Corning Incorporated Glass compositions having high thermal and chemical stability and methods of making thereof
US20070191207A1 (en) * 2006-02-10 2007-08-16 Danielson Paul S Glass compositions having high thermal and chemical stability and methods of making thereof
US20110201490A1 (en) * 2009-08-21 2011-08-18 Barefoot Kristen L Crack and scratch resistant glass and enclosures made therefrom
USRE47837E1 (en) 2009-08-21 2020-02-04 Corning Incorporated Crack and scratch resistant glass and enclosures made therefrom
USRE49530E1 (en) 2009-08-21 2023-05-16 Corning Incorporated Crack and scratch resistant glass and enclosures made therefrom
US9290407B2 (en) 2009-08-21 2016-03-22 Corning Incorporated Crack and scratch resistant glass and enclosures made therefrom
US8586492B2 (en) * 2009-08-21 2013-11-19 Corning Incorporated Crack and scratch resistant glass and enclosures made therefrom
US8975199B2 (en) * 2011-08-12 2015-03-10 Corsam Technologies Llc Fusion formable alkali-free intermediate thermal expansion coefficient glass
US9643883B2 (en) 2011-08-12 2017-05-09 Corsam Technologies Llc Fusion formable alkali-free intermediate thermal expansion coefficient glass
US9309139B2 (en) 2013-02-15 2016-04-12 Corning Incorporated High volume production of display quality glass sheets having low zirconia levels
US9370902B2 (en) 2013-10-03 2016-06-21 Comerstone Research Group, Inc. Fiber-reinforced epoxy composites and methods of making same without the use of oven or autoclave
US11034611B2 (en) 2014-05-20 2021-06-15 Corning Incorporated Scratch resistant glass and method of making
US9670088B2 (en) 2014-05-20 2017-06-06 Corning Incorporated Scratch resistant glass and method of making
US10509307B2 (en) 2014-07-30 2019-12-17 Corning Incorporated High contrast, glass-based, writeable/erasable front projection screens
WO2016018861A1 (en) 2014-07-30 2016-02-04 Corning Incorporated High contrast, glass-based, writeable/erasable front projection screens
US10167379B1 (en) 2014-10-06 2019-01-01 Cornerstone Research Group, Inc. Hybrid fiber layup and fiber-reinforced polymeric composites produced therefrom
US10946594B1 (en) 2017-01-06 2021-03-16 Cornerstone Research Group, Inc. Reinforced polymer-infused fiber composite repair system and methods for repairing composite materials

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