Classifications

• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/078—Glass compositions containing silica with 40% to 90% silica, by weight containing an oxide of a divalent metal, e.g. an oxide of zinc
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/083—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound
  • C03C3/085—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound containing an oxide of a divalent metal
  • C03C3/087—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound containing an oxide of a divalent metal containing calcium oxide, e.g. common sheet or container glass
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
  • C03C3/091—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
  • C03C3/091—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
  • C03C3/093—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium containing zinc or zirconium
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
  • H01J29/00—Details of cathode-ray tubes or of electron-beam tubes of the types covered by group H01J31/00
  • H01J29/86—Vessels; Containers; Vacuum locks
  • H01J29/863—Vessels or containers characterised by the material thereof
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
  • H01J2329/00—Electron emission display panels, e.g. field emission display panels
  • H01J2329/86—Vessels
  • H01J2329/8605—Front or back plates
  • H01J2329/8615—Front or back plates characterised by the material

Definitions

• the present invention relates to glass compositions suitable for being transformed into a glass ribbon, in particular by the “Float” process, from which heat-resistant plates can be cut. These plates can be used in particular for the production of substrates used in the manufacture of emissive screens such as plasma screens, electroluminescent screens and cold cathode screens (Field Emission Display - FED), or fire-resistant glazing.
• emissive screens such as plasma screens, electroluminescent screens and cold cathode screens (Field Emission Display - FED), or fire-resistant glazing.
• the glass used to produce such substrates is a glass belonging to the family of soda-lime-silica glasses, commonly used to form glazing intended for buildings or motor vehicles. If this type of glass is satisfactory with regard to chemical resistance, flatness and the defects it contains, on the other hand the level of performance in terms of yellowing ability proves to be insufficient for the intended application.
• the substrate is subjected to several treatments which aim to stabilize its dimensions and to fix a series of layers of different compounds, such as enamels, deposited on its surface.
• the substrate is generally heat treated at a temperature above 550 ° C.
• it is important to ensure that the coefficient of expansion of the glass used is of the same order of magnitude as that of the compounds deposited on its surface so as to avoid the appearance of cracks.
• the soda-lime-silica glass generally has a suitable coefficient of expansion, on the other hand its temperature resistance is insufficient and it is necessary to place it on a rectified slab to avoid any deformation during heat treatments.
• the glasses used for the manufacture of fire-resistant glazing belong to the category of borosilicate glasses. These glasses, which have good resistance to heat and thermal shock, are characterized by a relatively low coefficient of expansion. As a result, the mechanical strength of this type of glass cannot be improved significantly by thermal toughening because it is not allowed to have the development of high stresses in the glass. Glass compositions making it possible to obtain plates or substrates with practically zero deformation during heat treatments of the order of 550 to 600 ° C. and capable of undergoing thermal toughening are described in WO-A-96/11887. These are glass compositions having the desired properties for plasma screens that use little or no Al 2 O 3 alumina (0 to 18%), a high level of ZrO zirconia (6.5 to 20%) and an SiO 2 content not exceeding 63%.
• FR-A-2 578 550 are also described compositions making it possible to provide thermally stable substrates which combine alumina (0 to 5%) and zirconia (5 to 10%).
• the present invention aims to provide a glass composition for manufacturing a plate or a substrate having improved resistance to yellowing, and which retains the properties mentioned above, in particular a coefficient of thermal expansion ⁇ at least equivalent to silica glasses. known soda-lime.
• the subject of the invention is a glass composition intended for the manufacture of thermally stable substrates or plates which comprises the following constituents, in the following weight proportions:
• composition having a coefficient of thermal expansion between 80 and 90 x 10 "7 / ° C, in particular less than 85 x 10 " 7 / ° C, and preferably between 81 and 84 x 10 "7 / ° C.
• the substrates or the plates obtained from the compositions in accordance with the invention are capable of undergoing the heat treatments necessary for their application, for example as a plasma screen, and have a lower degree of yellowing compared to silico glasses. -sodo-lime.
• the improvement in the aging of the glass consisting in limiting the appearance of the yellow coloration is however not obtained at the expense of the other properties of the glass.
• the reduction of yellowing is based on the choice of a high SiO 2 content.
• glasses whose coefficient of thermal expansion remains of the same order of magnitude as that of a traditional silica-soda-lime glass know that it is between 80 and 90 x 10 "7 / ° C, in particular less than 85 x 10 " 7 / ° C, and preferably between 81 and 84 x 10 "7 / ° C measured at a temperature included between 20 and 300 ° C.
• the combination of the aforementioned constituents also makes it possible to obtain glasses having a lower annealing temperature ("strain point") greater than 570 ° C., preferably 580 ° C., a temperature which is at least approximately 70 ° C. higher than that a traditional silica-soda-lime glass. It is known that the glass no longer has any viscous behavior below the strain point corresponding to the temperature at which the glass has a viscosity of the order of 10 14 ' 5 poises. In fact, the strain point is an interesting benchmark for evaluating the temperature resistance of a glass. The strain point of the glasses according to the invention is comparable to that which is obtained for other glasses known for making screens (see WO 96/11 887 and FR 2 758 550).
• the glasses according to the invention generally have a density at 25 ° C. of less than
• the glasses according to the invention are well suited to the melting techniques associated with the "Float” process which operates by floating the glass on a bath of molten metal, in particular of tin. They only cause very slight corrosion of refractories, of the AZS type
• the glasses according to the invention can be easily melted and transformed into glass ribbon at temperatures of the same order as those used for the manufacture of a conventional soda-lime-silica glass.
• liquidus temperature T ⁇ q corresponding to the melting temperature of the vitrifiable raw materials of at most 1180 ° C, in particular between 1130 and 1170 ° C.
• This bearing although narrow, is sufficient to ensure forming in good conditions without major risk in particular in terms of the operation of the furnace.
• the role of the constituents entering into the glass composition according to the invention is defined below.
• SiO 2 plays an essential role. Its content is necessarily equal to or greater than 67%, without however exceeding 75%; beyond this, the melting of the batch and the refining of the glass require high temperatures which cause premature wear of the refractories of the furnace. Below 67% by weight of silica, the performance of the glass, in particular in terms of yellowing, is reduced.
• the glasses which are best suited to the conditions of floating on a bath of molten metal and have the best properties, comprise between 67 and 71% of SiO 2 .
• Alumina plays a stabilizing role. It contributes to increase the chemical resistance of the glass and the strain point.
• ZrO 2 also plays a stabilizing role. This oxide increases to some extent the chemical resistance of the glass and promotes the increase in the strain point. The percentage of ZrO 2 generally does not exceed 7% so as not to penalize the merger. If this oxide is difficult to melt, it has the advantage of only moderately increasing the viscosity of the glasses according to the invention at high temperatures, unlike the others oxides such as silica or alumina.
• the use of ZrO 2 makes it possible to avoid introducing oxides such as B 2 O 3 into these glasses or to increase the amount of alkaline oxides, one of the effects of these oxides being to reduce the viscosity of the glass .
• Alumina and zirconia play fairly similar roles: the sum of the Al O 3 and ZrO 2 contents is preferably less than 6%.
• the oxides Na 2 O and K 2 O make it possible to maintain the melting temperature of the glasses and the viscosity at high temperatures within the limits indicated above. To do this, the sum of these oxides remains equal to or greater than 10%, preferably between 10 and 15%.
• the presence of Na 2 O and K 2 O makes it possible to considerably increase their chemical resistance, in particular their hydrolytic resistance, as well as their resistivity.
• the content of K 2 O which increases because this makes it possible to thin the glass without lowering the strain point too much.
• the weight ratio of the Na O content to the KO content is less than or equal to 0.7.
• the alkaline earth oxides have the overall effect of raising the strain point: as a general rule their total content, in particular of MgO, CaO, SrO, and BaO, is greater than 12%, preferably greater than or equal to 15%.
• the ability of the glasses to devitrify increases and can become incompatible with the conditions for manufacturing the glass by floating on a molten metal bath. It is essentially CaO and MgO which increase the value of the strain point.
• the content by weight of CaO and MgO does not exceed 5% and 10%, respectively.
• BaO and SrO increase the chemical resistance of the glass and BaO also has the effect of reducing the melting temperature and the viscosity at high temperatures.
• Boron oxide, B 2 O 3 is optional. This network forming oxide can be added to or substituted for SiO 2 . It reduces the melting temperature of the batch and the viscosity of the glass at high temperatures. It also reduces the ability of the glass to devitrify, in particular by avoiding the rise in temperature in liquidus.
• the preferred glass compositions according to the invention comprise the following constituents in the following proportions: SiO 2 67 - 75%
• the glass compositions according to the invention can be used for the manufacture of heat-resistant plates, in particular for forming substrates for screens of the plasma, electroluminescent or cold cathode type.
• These substrates can be obtained by cutting glass sheets from a continuous glass ribbon obtained by floating the glass on a molten metal bath. They can have a glass thickness varying from 0.5 mm to 10 mm.
• These plates can also be used for the manufacture of fire-resistant glazing, in particular also obtained by cutting a strip of float glass.
• compositions according to the invention will be better appreciated through the exemplary embodiments gathered in table 1 in the appendix.
• Examples 1 to 4 describe glass compositions in accordance with the invention.
• the glass of Example 5 corresponds to a conventional silica-soda-lime glass composition used to manufacture a glass ribbon according to the Float process.
• the glass of Example 6 is a glass sold under the name PD200 by ASAHI suitable for producing emissive screens.
• PD200 glass sold under the name PD200 by ASAHI suitable for producing emissive screens.
• b * is representative of the degree of yellowing of the glass. It is measured as follows:
• a layer of metallic silver is deposited on the surface of the glass according to the so-called “sputtering” method.
• the glass is then heated to 580 ° C at the speed of 10 ° C / min, kept at this temperature for 30 min and then cooled to room temperature at the speed of 5 ° / min.
• the glass is immersed in an HNO solution to remove the silver layer.
• the measurement of the chromatic coordinate b * is carried out under illuminant D65 by taking the colorimetric reference observer described by the International Commission on Lighting (CLE.) 1931.
• the degree of yellowing after heat treatment of the glasses according to the invention is significantly lower than that of the soda lime glass of Example 5 or the screen glass of Example 6 .
• the coefficient ⁇ retains a satisfactory value, greater than 80 ⁇ 10 -7 / ° C., comparable to the above-mentioned reference glasses.
• the strain point of the glasses according to the invention is much higher than that of soda-lime glass. calcic and improved compared to screen glass.

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• Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Geochemistry & Mineralogy (AREA)
• Materials Engineering (AREA)
• Organic Chemistry (AREA)
• Glass Compositions (AREA)
• Manufacture Of Electron Tubes, Discharge Lamp Vessels, Lead-In Wires, And The Like (AREA)

Applications Claiming Priority (2)

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• 2003
  • 2003-05-07 FR FR0305588A patent/FR2854627B1/fr not_active Expired - Fee Related
• 2004
  • 2004-05-07 CN CNB2004800120328A patent/CN100376499C/zh not_active Expired - Fee Related
  • 2004-05-07 KR KR1020057020941A patent/KR20060006958A/ko not_active Application Discontinuation
  • 2004-05-07 US US10/555,098 patent/US20070037686A1/en not_active Abandoned
  • 2004-05-07 WO PCT/FR2004/001132 patent/WO2004099096A2/fr active Application Filing
  • 2004-05-07 EP EP04742689A patent/EP1631529A2/de not_active Withdrawn
  • 2004-05-07 JP JP2006505839A patent/JP2006525213A/ja active Pending
• 2008
  • 2008-04-07 US US12/098,590 patent/US20080188367A1/en not_active Abandoned
• 2009
  • 2009-09-08 US US12/555,092 patent/US20090325777A1/en not_active Abandoned

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