阅读说明：本技术 玻璃基板及其制造方法 (Glass substrate and method for manufacturing same ) 是由 梅村博通 于 2018-12-28 设计创作，主要内容包括：本发明的技术问题在于提供一种由于热收缩率小而适合作为高清晰的显示器基板并且不易引起剥离带电的玻璃基板及其制造方法。本发明的玻璃基板以质量百分比计含有50～70％的SiO<Sub>2</Sub>、10～25％的Al<Sub>2</Sub>O<Sub>3</Sub>、0％以上且小于3％的B<Sub>2</Sub>O<Sub>3</Sub>、0～10％的MgO、0～15％的CaO、0～10％的SrO、0～15％的BaO以及0.005～0.3％的Na<Sub>2</Sub>O,β-OH值小于0.18/mm,应变点为735℃以上。(The present invention addresses the problem of providing a glass substrate which has a low thermal shrinkage rate, is suitable as a high-definition display substrate, and is less likely to be electrically charged by peeling, and a method for manufacturing the same. The glass substrate of the invention contains 50-70% SiO by mass percentage 2 10 to 25% of Al 2 O 3 More than 0% and less than 3% of B 2 O 3 0 to 10% of MgO, 0 to 15% of CaO, 0 to 10% of SrO, 0 to 15% of BaO and 0.005 to 0.3% ofNa 2 O, β -OH value is less than 0.18/mm, and strain point is above 735 ℃.)

1. A glass substrate characterized in that a glass substrate,

comprises the following components in percentage by mass: 50-70% of SiO₂10 to 25% of Al₂O₃More than 0% and less than 3% of B₂O₃0 to 10% of MgO, 0 to 15% of CaO, 0 to 10% of SrO, 0 to 15% of BaO and 0.005 to 0.3% of Na₂O，

beta-OH value less than 0.18/mm and strain point over 735 deg.c.

2. The glass substrate according to claim 1,

contains 0.005-0.1% by mass of Fe₂O₃。

3. Glass substrate according to claim 1 or 2,

0.001-0.5% SnO₂。

4. The glass substrate according to any one of claims 1 to 3,

the Young's modulus is 80GPa or more.

5. The glass substrate according to any one of claims 1 to 4,

the heat shrinkage is 20ppm or less.

6. The glass substrate according to any one of claims 1 to 5,

has a dimension of 1500mm or more in the short side and 1850mm or more in the long side.

7. The glass substrate according to any one of claims 1 to 6,

the thickness is less than 0.7 mm.

8. The glass substrate according to any one of claims 1 to 7,

at least one surface is a fine concave-convex surface.

9. The glass substrate according to claim 8,

the surface roughness Ra of the fine concave-convex surface is 0.1-10 nm.

10. A method for manufacturing a glass substrate, comprising:

a raw material preparation step of preparing a glass batch prepared so as to obtain a glass containing 50 to 70 mass% of SiO₂10 to 25% of Al₂O₃More than 0% and less than 3% of B₂O₃0 to 10% of MgO, 0 to 15% of CaO, 0 to 10% of SrO,0 to 15% of BaO and 0.005 to 0.3% of Na₂O；

A melting step of melting glass batch materials by an electric melting furnace;

a forming step of forming molten glass into a plate shape;

an annealing step of annealing the plate-like glass by an annealing furnace; and

a processing step of cutting the annealed sheet glass into a predetermined size,

the method for producing a glass substrate can produce a glass substrate having a beta-OH value of less than 0.18/mm and a strain point of 735 ℃ or higher.

11. The method for manufacturing a glass substrate according to claim 10,

the cooling rate of the plate-like glass in the annealing step is an average cooling rate of 50 ℃/min to 1000 ℃/min within a temperature range from the annealing point to (the annealing point-100 ℃).

12. The method for manufacturing a glass substrate according to claim 10 or 11,

at least one surface is chemically etched.

13. The method for manufacturing a glass substrate according to claim 10 or 11,

at least one surface is physically abraded.

14. The method for manufacturing a glass substrate according to claim 12 or 13,

the surface roughness Ra is 0.1-10 nm.

Technical Field

The present invention relates to a glass substrate suitable for a high-definition display and less likely to cause electrostatic charging even when peeled off after being brought into contact with another member, and a method for manufacturing the same.

Background

Conventionally, glass has been widely used as substrates for flat panel displays such as liquid crystal displays, hard disks, filters, sensors, and the like. In recent years, high-definition displays such as low-temperature polysilicon TFTs and organic ELs have been actively developed and partially put into practical use on the basis of conventional liquid crystal displays.

The following characteristics (1) to (5) are particularly required for a glass substrate used for a high-definition display.

(1) Is alkali-free glass. That is, when the content of the alkali metal oxide in the glass substrate is large, alkali ions diffuse into the semiconductor material formed during the heat treatment, and the film characteristics deteriorate.

(2) Low thermal shrinkage and excellent thermal stability. That is, the glass substrate is heat-treated at several hundred degrees in the steps of film formation, annealing, and the like. When the glass substrate is thermally shrunk during the heat treatment, pattern misalignment and the like are likely to occur. For example, in a process for manufacturing a low-temperature polysilicon TFT, there is a heat treatment process at 400 to 600 ℃, in which a glass substrate is thermally shrunk to cause dimensional change. If this dimensional change is large, the pixel pitch of the TFT varies, which causes display defects. In the case of organic EL, even if there is a slight dimensional change, display defects may occur, and a glass substrate having an extremely low thermal shrinkage rate is required.

(3) The Young's modulus is higher than the Young's modulus in order to suppress the trouble caused by the deflection of the glass substrate.

(4) From the viewpoint of glass production, the glass composition is excellent in meltability and devitrification resistance.

(5) Has chemical resistance and etching performance required in the display manufacturing process.

Patent document 1 proposes an alkali-free glass substrate suitable for a high-definition display.

Disclosure of Invention

Technical problem to be solved by the invention

As described above, for the glass substrate used for the display, an alkali-free glass substrate containing no alkali metal oxide is used, but electrostatic charging may be a problem. Glass as an insulator is inherently very easily charged, whereas alkali-free glass is particularly easily charged, and tends to keep the already charged static electricity from escaping. In a manufacturing process of a liquid crystal display or the like, electrification of a glass substrate is caused in various processes, and electrification caused by peeling after the glass substrate is brought into contact with a metal or insulator plate in a process such as a film forming process is called peeling electrification. The peeling electrification of the glass substrate occurs not only in a step in which the glass substrate is peeled off in an atmosphere at normal pressure but also in a step in which a thin film on the surface of the substrate is etched, a step in which the glass substrate is vacuum such as a film forming step, and the like. When the conductive material approaches the charged glass substrate, discharge occurs. Further, since the voltage of the charged static electricity also reaches several 10kV, the discharge causes destruction (dielectric breakdown or electrostatic breakdown) of elements, electrode lines, or the glass substrate itself on the surface of the glass substrate, which causes display failure. In liquid crystal displays, particularly low temperature polysilicon TFT displays, a minute semiconductor element such as a thin film transistor and an electronic circuit are formed on the surface of a glass substrate, and the element and the circuit are particularly problematic because they are very vulnerable to electrostatic breakdown. In addition, dust present in a charged environment is also attracted to cause contamination of the substrate surface.

As a countermeasure against static electricity for a glass substrate, a method of neutralizing electric charges using an ionizer, a method of discharging accumulated electric charges into the air by raising the temperature in the environment, or the like is known. However, these measures not only cause an increase in cost, but also have a problem in that effective measures are difficult to be implemented because the place where charging is caused in the process is complicated. These methods cannot be used in a vacuum process such as a plasma process. Therefore, glass substrates that are not easily charged are strongly demanded for flat panel display applications, such as liquid crystal displays.

The present invention addresses the problem of providing a glass substrate which is suitable as a high-definition display substrate due to its low heat shrinkage rate and is less likely to be electrically peeled off.

Means for solving the problems

The glass substrate of the present invention, which is created to solve the above problems, is characterized by comprising, in mass percent: 50-70% of SiO₂10 to 25% of Al₂O₃More than 0% and less than 3% of B₂O₃0 to 10% of MgO, 0 to 15% of CaO, 0 to 10% of SrO, 0 to 15% of BaO and 0.005 to 0.3% of Na₂O, β -OH value is less than 0.18/mm, and strain point is above 735 ℃.

Further, a method for manufacturing a glass substrate according to the present invention includes: a raw material preparation step of preparing a glass batch prepared so as to obtain a glass containing 50 to 70 mass% of SiO₂10 to 25% of Al₂O₃More than 0% and less than 3% of B₂O₃0 to 10% of MgO, 0 to 15% of CaO, 0 to 10% of SrO, 0 to 15% of BaO and 0.005 to 0.3% of Na₂O, a melting step of melting a glass batch by an electric melter, a forming step of forming the molten glass into a plate shape, an annealing step of annealing the plate-shaped glass by an annealing furnace, and a processing step of cutting the annealed plate-shaped glass into a predetermined size, wherein a glass substrate having an β -OH value of less than 0.18/mm and a strain point of 735 ℃ or higher is obtained by the method for producing a glass substrate.

According to the findings of the present inventors, in the alkali-free glass substrate, the heat shrinkage rate is reduced as the β -OH value is reduced, but if the β -OH value is less than 0.18/mm, charging becomes remarkably easy, whereas according to the present invention, although the β -OH value is less than 0.18/mm, the resistivity of the glass is increased by containing 0.005 mass% or moreReduced action of Na₂O, therefore, electrification of the glass substrate can be suppressed. On the other hand, if B is contained in a large amount₂O₃The glass contains Na₂O, B when the glass is melted₂O₃Readily volatile in the form of sodium compounds. Therefore, in the present invention, B is₂O₃Limiting the content to less than 3% by mass, and suppressing B in glass melting₂O₃Volatilize to realize Na in the glass₂Stabilization of the amount of O. Thus, a glass substrate having a low thermal shrinkage ratio and being less likely to be electrically charged can be stably obtained.

The "β -OH value" refers to a value obtained by measuring the transmittance of the glass using FT-IR and using the following formula.

beta-OH value ═ (1/X) log (T1/T2)

X: glass thickness (mm)

T1: reference wavelength 3846cm^-1Transmittance (%)

T2: hydroxyl absorption wavelength of 3600cm^-1Near minimum transmittance (%)

In the present invention, as a method for lowering the β -OH value of a glass substrate, (1) a method of selecting a glass batch having a low water content (a glass raw material having a low water content, a cullet obtained by finely pulverizing a glass body having a low water content), and (2) a method of adding a component (Cl, SO) having an action of reducing the water content in the glass₃Etc.). (3) The moisture content in the furnace atmosphere is reduced. (4) N in molten glass₂Bubbling. (5) A small melting furnace is used. (6) The flow rate of the molten glass is increased. (7) An electric melting furnace is adopted.

In the case where the glass substrate of the present invention is produced as described above, it is preferable to use a glass batch having a low water content as much as possible and use an electric melter, from the viewpoint of reducing the β -OH value. When melting glass batch materials using an electric melter, the increase in the moisture content of the atmosphere due to gas combustion in the melting furnace or the like can be suppressed, and therefore the moisture content in the molten glass can be easily reduced as compared with a gas combustion furnace. Therefore, the β -OH value of the glass produced in the electric melter is reduced. Further, as the β — OH value decreases, the strain point of the glass increases, and a glass substrate having a low thermal shrinkage rate can be easily obtained. The electric melter is preferably a complete electric melter not using a burner, but may be an electric melter provided with a burner or a heater for performing radiant heating in an auxiliary manner at the initial stage of melting.

In the present invention, the thermal shrinkage of the glass substrate is preferably 20ppm or less, 15ppm or less, 12ppm or less, 10ppm or less, 9ppm or less, 8ppm or less, 7ppm or less, 6ppm or less, and particularly preferably 5ppm or less. However, when the thermal shrinkage of the glass substrate is 0ppm, the productivity is remarkably reduced, and therefore, it is preferably 1ppm or more, 2ppm or more, and particularly preferably 3ppm or more. The deviation of the thermal shrinkage of the glass substrate from the target value is preferably ± 1.0ppm or less, and particularly preferably ± 0.5ppm or less. If the thermal shrinkage rate of the glass substrate is high, display defects of displays such as low-temperature polysilicon TFTs and organic EL are likely to occur, and if the variation in thermal shrinkage rate of the glass substrate is large, the display substrate cannot be stably produced. In order to reduce the variation in the thermal shrinkage rate of the glass substrate, the moisture content of the glass raw material may be adjusted or the cooling rate in the annealing step may be adjusted.

The method for forming the glass substrate of the present invention is not particularly limited, and a float method is preferable from the viewpoint of enabling the annealing process to be extended, and a down-draw method is preferable from the viewpoint of improving the surface quality of the glass substrate or reducing the thickness thereof, and an overflow down-draw method is particularly preferable. In the overflow downdraw method, the surface of the glass substrate to be the front and back surfaces is formed in a free surface state without contacting the molding. Therefore, a glass substrate having an overflow converging surface at the center in the thickness direction and hot forged surfaces on both surfaces was obtained. Thus, a glass substrate which is not polished and has excellent surface quality (small surface roughness and undulation) can be produced at low cost.

In the present invention, when the down draw method is employed, the length (height difference) of the annealing furnace is preferably 3m or more. The annealing step is a step for removing strain of the glass substrate, and the longer the annealing furnace is, the easier the cooling rate of the plate-shaped glass is adjusted, and the easier the thermal shrinkage rate of the glass substrate is reduced. Therefore, the length of the annealing furnace is preferably 5m or more, 6m or more, 7m or more, 8m or more, 9m or more, and particularly preferably 10m or more.

In the present invention, the cooling rate of the plate glass in the annealing step is preferably an average cooling rate of 50 to 1000 ℃/min, 100 to 800 ℃/min, 300 to 800 ℃/min within a temperature range from the annealing point to (annealing point-100 ℃). The thermal shrinkage of the glass substrate also varies depending on the cooling rate at the time of annealing the plate glass. That is, the heat shrinkage rate of the glass substrate after the rapid cooling is high, whereas the heat shrinkage rate of the glass substrate after the slow cooling is low.

In the present invention, the annealed plate glass is subjected to a cutting process. That is, the formed plate-like glass (glass ribbon) is cut into a predetermined size. Then, in order to prevent damage from the end surface portion, end surface grinding or end surface polishing may be performed. The short side of the glass substrate thus obtained is preferably 1500mm or more, and the long side is preferably 1850mm or more. That is, the larger the size of the glass substrate, the higher the production efficiency of the glass substrate, and therefore the shorter side is preferably 1950mm or more, 2200mm or more, 2800mm or more, and particularly preferably 2950mm or more, and the longer side is preferably 2250mm or more, 2500mm or more, 3000mm or more, and particularly preferably 3400mm or more.

In the present invention, the thickness of the glass substrate is preferably 0.7mm or less, 0.6mm or less, 0.5mm or less, and particularly preferably 0.4mm or less. The smaller the thickness, the lighter the glass substrate can be, and the more suitable it is for a portable display substrate. However, if the thickness of the glass substrate is too small, the glass substrate is easily damaged by peeling electrification, and therefore, it is preferably 0.1mm or more, and more preferably 0.2mm or more.

In order to further suppress peeling electrification of the glass substrate of the present invention, at least one surface is preferably a fine uneven surface. The surface shape of the fine uneven surface may be such that the surface roughness Ra is 0.1 to 10 nm. As a method for forming a fine uneven surface on the surface of the glass substrate, physical polishing using a polishing apparatus, or a chemical etching method by applying an etching solution or a spray etching gas to the glass substrate may be employed. The latter chemical etching is preferable because it is difficult for glass chips and the like to adhere to the glass substrate and enables cleaning of the surface. Since the glass substrate of the present invention is inherently less likely to be electrically charged by peeling, even when fine irregularities are formed on the surface thereof, the processing time can be shortened, and the productivity can be improved.

Effects of the invention

According to the present invention, a glass substrate which is suitable as a high-definition display substrate due to a low heat shrinkage rate and is less likely to be electrically charged by peeling can be stably obtained.

Drawings

Fig. 1 is an explanatory view showing a method of measuring the heat shrinkage rate of a glass substrate.

Fig. 2 is an explanatory view showing an apparatus for measuring a peeling electrification amount of a glass substrate, (a) is an explanatory view showing a state where the glass substrate is separated from a stage, and (b) is an explanatory view showing a state where the glass substrate is placed on the stage.

Description of the symbols

G glass sample (glass substrate)

M mark

1 supporting table

2 pad seat

3 working table

4 surface potential body

5 air gun with ionizer

Detailed Description

In the present specification, the numerical range expressed by the term "to" means a range including the numerical values described before and after the term "to" as the minimum value and the maximum value, respectively.

The glass substrate of the present invention contains, by mass: 50-70% of SiO₂10 to 25% of Al₂O₃More than 0% and less than 3% of B₂O₃0 to 10% of MgO, 0 to 15% of CaO, 0 to 10% of SrO, 0 to 15% of BaO and 0.005 to 0.3% of Na₂And O. The reason why the content of each glass constituent component is limited as described above will be described below. The following expression% of each component means mass% unless otherwise specified。

If SiO₂When the content (b) is small, chemical resistance, particularly acid resistance, is liable to be lowered, and strain point is liable to be lowered. Further, the density becomes high, and it is difficult to reduce the weight of the glass substrate. The density of the glass is preferably less than 2.70g/cm³And more preferably less than 2.65g/cm³. On the other hand, if SiO₂When the content (b) is more than the above range, the high-temperature viscosity becomes high and the meltability tends to be low. Further, SiO₂Crystals, particularly cristobalite, precipitate, and the liquidus viscosity, that is, the devitrification resistance is liable to decrease. Thus SiO₂Preferably 50% or more, 55% or more, 58% or more, 60.5% or more, more preferably 61% or more, preferably 70% or less, 65% or less, 64% or less, 63.5% or less, 63% or less, 62.5% or less, more preferably 62% or less.

If Al is present₂O₃When the content (b) is less, the strain point decreases, the thermal shrinkage rate increases, the young's modulus decreases, and the glass substrate is easily bent. On the other hand, if Al₂O₃When the content (b) is increased, the BHF (buffered hydrofluoric acid) resistance is lowered, the glass surface is likely to be clouded, and the crack resistance is lowered, so that the glass is likely to be broken. Further, SiO precipitates in the glass₂-Al₂O₃The liquidus viscosity is liable to decrease due to the precipitation of crystals, particularly mullite. Thus, Al₂O₃Is 10% or more, 13% or more, 15% or more, 16% or more, 17% or more, 17.5% or more, more preferably 18% or more, 25% or less, 23% or less, 21% or less, 20% or less, 19% or less, 19.7% or less, more preferably 19.5% or less.

B₂O₃The component acts as a flux and reduces viscosity to improve meltability. If B is₂O₃When the content (b) is increased, the molten glass volatilizes, and the glass component tends to change. In addition, B₂O₃The higher the content of (b), the lower the strain point, and the more easily the heat resistance and the acid resistance are reduced. Further, the young's modulus is lowered, and the amount of deflection of the glass substrate tends to be large. Thus, it is possible to provideB₂O₃Preferably less than 3%, 2% or less, 1.7% or less, 1.5% or less, 1.4% or less, and 1% or less, and more preferably substantially none. However, from the viewpoints of improving the melting property, preventing the BHF resistance and the crack resistance from being lowered, B₂O₃May be contained in an amount of 0.1% or more, 0.2% or more, 0.3% or more, 0.4% or more, and further 0.5% or more.

As described above, the β -OH value of glass is easily affected by moisture contained in a glass batch charged into a glass melting furnace, and particularly, a glass raw material as a boron source has hygroscopicity, and a glass raw material containing crystal water is also present, so that moisture is easily taken into glass₂O₃For the above reasons, in the present invention, it is preferable to reduce B as much as possible, because the smaller the content of (B) is, the more easily the β -OH value of the glass is reduced, and the lower the β -OH value is, the higher the strain point of the glass is, the more easily the thermal shrinkage of the glass substrate is reduced₂O₃It is desirable that B is substantially not contained₂O₃. Here, B is substantially not contained₂O₃Meaning that it intentionally does not contain B₂O₃The raw material does not prevent the impurities from being mixed in. Specifically, it means B₂O₃The content of (B) is 0.1% or less.

MgO is a component that lowers the high-temperature viscosity and improves the meltability, and among the alkaline earth metal oxides, MgO is a component that significantly improves the Young's modulus, but if it is introduced excessively, SiO is introduced₂Crystals, particularly cristobalite, precipitate, and the liquidus viscosity easily decreases. Further, MgO is a component that easily reacts with BHF to form a product. When the content of MgO is small, the above-described effects are hardly obtained, and when the content of MgO is large, devitrification resistance and strain point are easily lowered. Therefore, the content of MgO is preferably 10% or less, 9% or less, 8% or less, 6% or less, 5% or less, 4% or less, 3.5% or less, and particularly preferably 3% or less. Further, it is preferably 1% or more, 1.5% or more, and particularly preferably 2% or more.

CaO is a component that lowers the high-temperature viscosity without lowering the strain point and remarkably improves the meltability. In addition, since the raw materials to be introduced into the alkaline earth metal oxide are relatively inexpensive, the raw materials are inexpensive. If the CaO content is small, it is difficult to enjoy the above-described effects. On the other hand, if the content of CaO is too large, the glass is likely to devitrify and the thermal expansion coefficient is likely to increase. Therefore, the content of CaO is preferably 15% or less, 12% or less, 11% or less, 8% or less, and particularly preferably 6% or less. Further, it is preferably 1% or more, 2% or more, 3% or more, 4% or more, and particularly preferably 5% or more.

SrO is a component that suppresses phase separation of glass and improves resistance to devitrification. And a component that reduces the high-temperature viscosity without lowering the strain point, improves the meltability, and suppresses an increase in the liquidus temperature. If the SrO content is small, it is difficult to obtain the above-described effects. On the other hand, when the SrO content is increased, devitrification crystals of strontium silicate are likely to precipitate, and the resistance to devitrification is likely to decrease. Therefore, the SrO content is preferably 10% or less, 7% or less, 5% or less, 4% or less, and particularly preferably 3% or less. Further, it is preferably 0.1% or more, 0.2% or more, 0.3% or more, 0.5% or more, 1.0% or more, and particularly preferably 1.5% or more.

BaO is a component that significantly improves resistance to devitrification. If the content of BaO is small, it is difficult to enjoy the above-described effects. On the other hand, when the content of BaO is increased, the density becomes too high and the meltability is easily decreased. Further, devitrified crystals containing BaO are likely to precipitate, and the liquid phase temperature is likely to rise. Therefore, the content of BaO is preferably 15% or less, 14% or less, 13% or less, 12% or less, 11% or less, 10.5% or less, 10% or less, 9.5% or less, and particularly preferably 9% or less. Further, it is preferably 1% or more, 3% or more, 4% or more, 5% or more, 6% or more, and particularly preferably 7% or more.

Na₂O is a component for lowering the resistivity of the glass. If Na₂When the content of O is small, it is difficult to obtain the above-described effect. On the other hand, if Na₂When the content of O is increased, alkali ions diffuse into the formed semiconductor material during the heat treatment, and the film characteristics deteriorate. Thus, Na₂O is preferably 0.005% or more and 0.008% or moreUpper, 0.01% or more, 0.02% or more, 0.025% or more, 0.03% or more, more preferably 0.05% or more, preferably 0.3% or less, more preferably 0.2% or less.

As for removing Na₂An alkali metal oxide other than O may be added with K₂O。K₂O is also a component for lowering the resistivity of the glass. If K₂When the content of O is small, it is difficult to obtain the above-described effect. On the other hand, if K₂When the content of O is increased, alkali ions diffuse into the formed semiconductor material during the heat treatment, and the film characteristics deteriorate. Thus K₂O is preferably 0.001% or more, 0.002% or more, 0.005% or more, 0.01% or more, 0.02% or more, 0.025% or more, 0.03% or more, more preferably 0.05% or more, preferably 0.3% or less, and more preferably 0.2% or less. K₂O may contain Na₂More is O.

Further, Na may be added as appropriate₂O、K₂Alkali metal oxides other than O, i.e. Li₂And O. However, when the content of the alkali metal oxide is increased, alkali ions diffuse into the semiconductor material having been formed during the heat treatment, and the film characteristics deteriorate, and therefore, it is preferable to use the total amount of the alkali metal oxide (Na)₂O、Li₂O and K₂Total amount of O) is 0.4% or less.

In the present invention, the glass substrate may contain the following components in addition to the above components.

The glass substrate of the present invention preferably contains 0.005 to 0.1% of Fe₂O₃。Fe₂O₃With Na₂O is a component having an effect of lowering the resistivity of the glass, and contains a certain amount or more of Fe₂O₃Thereby, the effect of suppressing electrification of the glass substrate is further improved. Fe₂O₃The content is preferably 0.005% or more, 0.008% or more, and particularly preferably 0.01% or more. However, if Fe is contained in an amount exceeding 0.1%₂O₃Then, since the transmittance of the glass may be lowered and thus it may not be preferable as a display substrate, Fe₂O₃Preferably 0.1% or less.

The glass substrate of the present invention preferably contains 0.001 to 0.5% SnO₂。SnO₂Is a component having a good clarifying action in a high-temperature region, increasing the strain point and decreasing the high-temperature viscosity. In addition, in the case of an electric melting furnace using a molybdenum electrode, there is an advantage that the electrode is not corroded. On the other hand, if SnO₂When the content of (B) is increased, SnO₂The devitrification crystal of (2) is liable to precipitate and ZrO is liable to be promoted₂Precipitation of devitrified crystals. Thus, SnO₂The content of (B) is preferably 0.001 to 0.5%, 0.001 to 0.45%, 0.001 to 0.4%, 0.01 to 0.35%, 0.1 to 0.3%, and particularly preferably 0.15 to 0.3%.

Further, other components that the glass substrate of the present invention may contain will be described.

ZnO is a component for improving the meltability. However, when the content of ZnO is increased, the glass is easily devitrified and the strain point is easily lowered. The content of ZnO is preferably 0 to 5%, 0 to 4%, 0 to 3%, and particularly preferably 0 to 2%.

ZrO₂Is a component for improving chemical durability, but if ZrO₂When the content of (A) is increased, ZrSiO is easily generated₄The devitrified article of (1). ZrO (ZrO)₂The content of (b) is preferably 0 to 5%, 0 to 4%, 0 to 3%, and particularly preferably 0.01 to 2%.

TiO₂Is a component which lowers the high-temperature viscosity to improve the meltability and suppresses the coloring due to negative induction, but TiO is preferred₂When the content (b) is large, the glass is colored and the transmittance is liable to decrease. TiO 2₂The content of (b) is preferably 0 to 5%, 0 to 4%, 0 to 3%, 0 to 2%, and particularly preferably 0 to 0.1%.

P₂O₅Is a component which increases the strain point and suppresses the precipitation of devitrified crystals of alkaline earth metal silicate such as anorthite. However, if P is contained in a large amount₂O₅The glass is prone to phase separation. P₂O₅The content of (b) is preferably 0 to less than 0.15%, 0 to 1%, 0 to 0.1%, and particularly preferably not substantially contained, more specifically preferably less than 0.01%, from the viewpoint of easy reuse of the glass.

Cl、F、SO₃、C、CeO₂Or metal powder of Al, Si, etc. can be contained up to 3% in total. As₂O₃、Sb₂O₃The metal oxide may be used as a clarifying agent, but is desirably substantially not contained from the viewpoint of preventing corrosion of the environment and the electrode. As used herein, substantially not containing As means₂O₃And Sb₂O₃The total amount of (A) is 0.1% or less.

The glass substrate of the invention has a beta-OH value of less than 0.18/mm. Since the thermal shrinkage rate decreases as the beta-OH value of the glass decreases, the strain point of the glass increases, and the beta-OH value is preferably less than 0.15/mm, 0.12/mm or less, 0.1/mm or less, 0.07/mm or less, and particularly preferably 0.05/mm or less. However, from the viewpoint of suppressing the electrification of the glass substrate, the β -OH value is preferably 0.01/mm or more, 0.02/mm or more, and particularly preferably 0.03/mm or more.

The glass substrate of the present invention has a strain point of 735 ℃ or higher. In order to reduce the thermal shrinkage of the glass substrate, it is desirable to increase the strain point as much as possible, and it is preferably 740 ℃ or higher, 745 ℃ or higher, and more preferably 750 ℃ or higher. However, the strain point is preferably 800 ℃ or lower because the higher the temperature at the time of glass melting or forming increases the production cost of the glass substrate.

For the same reason as the strain point, the annealing point of the glass substrate of the present invention is preferably 780 ℃ or higher, 790 ℃ or higher, 800 ℃ or higher, 810 ℃ or higher, and particularly preferably 820 ℃ or higher. However, the higher the annealing point, the higher the temperature at the time of glass melting or forming, the more the manufacturing cost of the glass substrate increases, and therefore, the annealing point is preferably 850 ℃ or less, more preferably 840 ℃ or less.

The Young's modulus of the glass substrate of the present invention is preferably 80GPa or more. The higher the Young's modulus, the smaller the deflection of the glass substrate, and the easier the handling during transportation or packaging. The Young's modulus is preferably 81GPa or more, 82GPa or more, 83GPa or more, 84GPa or more, and more preferably 85GPa or more.

Equivalent to 10 of the glass substrate of the present invention^4.5The temperature of dPa · s is preferably 1330 DEG CAt a temperature of 1320 ℃ or lower, and particularly preferably 1310 ℃ or lower. If it is 10^4.5When the temperature of dpas is high, the temperature at the time of molding becomes too high, and the production yield tends to decrease.

Equivalent to 10 of the glass substrate of the present invention^2.5The temperature of dPa · s is preferably 1670 ℃ or lower, 1660 ℃ or lower, and particularly preferably 1650 ℃ or lower. If it is 10^2.5When the temperature of dpas is increased, the glass becomes hard to melt, defects such as bubbles are likely to increase, and the production yield is likely to decrease.

The glass substrate of the present invention preferably has a liquidus temperature of less than 1250 ℃, less than 1240 ℃, less than 1230 ℃, and more preferably less than 1220 ℃. Thus, devitrification crystals are less likely to occur during glass production, and therefore, the glass can be easily formed into a plate shape by the overflow downdraw method. This can improve the surface quality of the glass substrate and suppress a reduction in the production yield. From the viewpoint of increasing the size of a glass substrate and increasing the definition of a display, it is very important to improve the devitrification resistance of glass and to suppress as much as possible devitrified substances which may become surface defects.

The glass substrate of the present invention preferably has a viscosity of 10 at the liquidus temperature^4.910 dPas or more^5.0dPa·s、10^5.110 dPas or more^5.2dPas or more, particularly preferably 10^5.3dPas or more. Thus, devitrification is less likely to occur during glass forming, so that the glass can be easily formed into a plate shape by the overflow down-draw method, and the surface quality of the glass substrate can be improved. The viscosity at the liquidus temperature is an index of moldability, and the higher the viscosity at the liquidus temperature, the higher the moldability.