GLASS DISK FOR MAGNETIC RECORDING MEDIUM AND MAGNETIC RECORDING DEVICE USING THE SAME

Information

  • Patent Application
  • 20230162759
  • Publication Number
    20230162759
  • Date Filed
    May 18, 2021
    4 years ago
  • Date Published
    May 25, 2023
    a year ago
Abstract
A glass disk for a magnetic recording medium of the present invention has a disk shape, and has a strain point of 695° C. to 780° C., a temperature at 104.5 dPa·s of 1300° C. or lower, and a Young's modulus of 78 GPa or higher.
Description
TECHNICAL FIELD

The present invention relates to a glass disk for a magnetic recording medium and a magnetic recording device using the same.


BACKGROUND ART

A magnetic recording device includes a magnetic recording medium in which a magnetic layer is formed on a magnetic recording medium substrate, and can record information using the magnetic layer. In the related art, an aluminum alloy substrate is used as the magnetic recording medium substrate used in the magnetic recording device. At present, with a demand for a high recording density, thinning of a magnetic medium substrate is studied. However, when an aluminum alloy substrate is thinned, rigidity is lost, and thus attention is focused on a glass disk (a glass substrate) excellent in rigidity, flatness, smoothness, and the like.


In recent years, in order to meet a need for a higher recording density, a magnetic recording medium using an energy-assisted magnetic recording method, that is, an energy-assisted magnetic recording medium is studied. Also in the energy-assisted magnetic recording medium, a glass disk is used, and a magnetic layer or the like is formed on a surface of the glass disk. In the energy-assisted magnetic recording medium, an ordered alloy having a large magnetic anisotropy coefficient Ku (hereinafter referred to as a “high Ku”) is used as a magnetic material of the magnetic layer.


In order to increase a degree of ordering (regularity) of the magnetic layer and achieve the high Ku, a base material including the glass disk may be heat-treated at a high temperature of about 800° C. at the time of film formation of the magnetic layer, or before or after the film formation. As a recording density is higher, the heat treatment temperature needs to be higher, and thus higher heat resistance than that of the related-art glass disk for a magnetic recording medium is required. After the magnetic layer is formed, laser irradiation may be performed on the base material including the glass disk. Such heat treatment and laser irradiation are also intended to increase an annealing temperature and coercive force of a magnetic layer containing a FePt-based alloy or the like.


SUMMARY OF INVENTION
Technical Problem

A glass disk for a magnetic recording medium is required to have high rigidity (Young's modulus) in order not to cause large deformation at the time of high-speed rotation. More specifically, in a disk-shaped magnetic recording medium, information is written and read along a rotation direction while the medium is rotated at a high speed around a central axis and a magnetic head is moved in a radial direction. In recent years, a rotational speed for increasing a writing speed and a reading speed is increasing from 5400 rpm to 7200 rpm, and further to 10000 rpm, but in the disk-shaped magnetic recording medium, a position for recording information is assigned in advance according to a distance from the central axis. Therefore, when a glass disk is deformed during rotation, the magnetic head is displaced, which makes accurate reading difficult.


In recent years, by mounting a dynamic flying height (DFH) mechanism on a magnetic head, a gap between a recording and reproducing element portion of the magnetic head and a surface of a magnetic recording medium is greatly narrowed (a flying height is reduced), and a higher recording density is achieved. The DFH mechanism is a mechanism in which a heating unit such as an extremely small heater is provided in the vicinity of the recording and reproducing element portion of the magnetic head, and a periphery of the element portion is alone thermally expanded toward a medium surface direction. By providing such a mechanism, a distance between the magnetic head and a magnetic layer of the medium is reduced, and thus signals of smaller magnetic particles can be picked up, and a high recording density can be achieved. On the other hand, the gap between the recording and reproducing element portion of the magnetic head and the surface of the magnetic recording medium is extremely small, for example, 2 nm or less, and thus the magnetic head may collide with the surface of the magnetic recording medium even with a slight impact. As a rotation speed is higher, this tendency is more remarkable. Therefore, it is important to prevent occurrence of bending and flapping (fluttering) of a glass disk which may cause the collision at the time of high-speed rotation.


Further, with a recent increase in use of data centers and servers worldwide, it is required to reduce the cost of these glass disks. Formability is important for reducing the cost of the glass disks. Further, it is also effective to adopt an overflow down-draw method or a float method to form a large glass substrate with a thickness close to a thickness of a product and process the large glass substrate into a circular disc shape.


The present invention has been made in view of the above circumstances, and an object of the present invention is to devise a glass disk for a magnetic recording medium that is less likely to cause bending and flapping (fluttering) at the time of high-speed rotation, has sufficient heat resistance to achieve a very high recording density, and contributes to cost reduction.


Solution to Problem

As a result of repeating various experiments, the present inventors have found that the above-described technical problems can be solved by strictly regulating glass properties of a glass disk, and have proposed the present invention. That is, a glass disk for a magnetic recording medium of the present invention has a disk shape, and has a strain point of 695° C. to 780° C., a temperature at 104.5 dPa·s of 1300° C. or lower, and a Young's modulus of 78 GPa or higher. In the glass disk for a magnetic recording medium of the present invention, a circular opening is preferably formed in a central portion. Here, the term “strain point” refers to a value measured based on a method of ASTM C336. The term “temperature at 104.5 dPa·s” refers to a value measured by a platinum sphere pull up method. The term “Young's modulus” may be measured by a known resonance method.


The FIGURE is an upper perspective view showing a disk shape. The disk shape refers to a circular disc shape, and is preferably a shape in which a circular opening is formed in a central portion (see the FIGURE).


In the glass disk for a magnetic recording medium of the present invention, the strain point is regulated to 695° C. or higher. Accordingly, even when heat treatment at a high temperature such as thermal assist or laser irradiation is performed, the glass disk is less likely to be deformed. As a result, a higher heat treatment temperature can be adopted when achieving a high Ku, and thus a magnetic recording device having a high recording density can be easily manufactured.


In addition, in the glass disk for a magnetic recording medium of the present invention, the temperature at a viscosity in high temperature of 104.5 dPa·s is regulated to 1300° C. or lower. Accordingly, formability is improved, which can contribute to cost reduction of the glass disk.


Further, in the glass disk for a magnetic recording medium of the present invention, the Young's modulus is regulated to 78 GPa or higher. Accordingly, bending and flapping (fluttering) of the glass disk are less likely to occur at the time of high-speed rotation, and thus a collision between an information recording medium and a magnetic head can be prevented.


The glass disk for a magnetic recording medium of the present invention preferably contains, as a glass composition, in terms of mol %, 60% to 71% of SiO2, 10% to 16% of Al2O3, 0% to 5% of B2O3, 0% to 0.1% of Na2O, 0% to 1% of K2O, 0% to 12% of MgO, 0% to 12% of CaO, 0% to 10% of SrO, 0% to 10% of BaO, 0% to 1% of ZrO2, and 0% to 1% of SnO2.


In the glass disk for a magnetic recording medium of the present invention, an average surface roughness Ra of a surface is preferably 1.0 nm or less. Accordingly, magnetic properties can be improved even if a bit size is miniaturized for a high recording density. Here, the term “average surface roughness Ra of a surface” refers to an average surface roughness Ra of main surfaces (both surfaces) excluding end surfaces, and can be measured by, for example, an atomic force microscope (AFM).


In the glass disk for a magnetic recording medium of the present invention, an average linear transmittance in an optical path length of 1 mm and a wavelength range of 350 nm to 1500 nm is preferably 70% or more.


In the glass disk for a magnetic recording medium of the present invention, a magnetic layer is preferably provided on a surface. Accordingly, it is easy to apply the glass disk to an energy-assisted magnetic recording medium.


A glass substrate for a magnetic recording medium of the present invention has a strain point of 695° C. to 740° C., a temperature at 1045 dPa·s of 1300° C. or lower, and a Young's modulus of 78 GPa or higher.


The glass substrate for a magnetic recording medium of the present invention preferably contains, as a glass composition, in terms of mol %, 60% to 71% of SiO2, 10% to 16% of Al2O3, 0% to 5% of B2O3, 0% to 0.1% of Na2O, 0% to 1% of K2O, 0% to 12% of MgO, 0% to 12% of CaO, 0% to 10% of SrO, 0% to 10% of BaO, 0% to 1% of ZrO2, and 0% to 1% of SnO2.


A magnetic recording device of the present invention preferably includes the above-described glass disk for a magnetic recording medium.





BRIEF DESCRIPTION OF DRAWINGS

The FIGURE is an upper perspective view showing a disk shape.





DESCRIPTION OF EMBODIMENTS

In a glass disk for a magnetic recording medium of the present invention, a strain point is 695° C. or higher, preferably 697° C. or higher, 700° C. or higher, 702° C. or higher, 705° C. or higher, 710° C. or higher, 711° C. or higher, 712° C. or higher, 713° C. or higher, 714° C. or higher, and particularly 715° C. or higher. When the strain point is too low, it is difficult to perform heat treatment at a high temperature and laser irradiation, and it is difficult to manufacture a magnetic recording medium having a high recording density. On the other hand, when the strain point is too high, a melting temperature and a forming temperature are high, and thus production efficiency of a glass substrate is likely to be decreased. Therefore, the strain point is 780° C. or lower, preferably 775° C. or lower, 770° C. or lower, 768° C. or lower, 765° C. or lower, 763° C. or lower, 760° C. or lower, 758° C. or lower, 755° C. or lower, 753° C. or lower, 750° C. or lower, 748° C. or lower, 745° C. or lower, 743° C. or lower, 740° C. or lower, 738° C. or lower, 735° C. or lower, 733° C. or lower, 730° C. or lower, 725° C. or lower, 720° C. or lower, and particularly 715° C. or lower. A most preferred range of the strain point is 715° C. to 770° C.


In the glass disk for a magnetic recording medium of the present invention, as a temperature at a viscosity in high temperature of 1045 dPa·s is lower, a load applied to forming equipment can be more reduced. The temperature at 1045 dPa·s is 1300° C. or lower, preferably 1290° C. or lower, 1280° C. or lower, 1275° C. or lower, 1270° C. or lower, 1265° C. or lower, 1260° C. or lower, 1255° C. or lower, and particularly 1250° C. or lower. On the other hand, when the temperature at 1045 dPa·s is too low, the strain point cannot be designed to be high. Therefore, the temperature at 1045 dPa·s is preferably 1150° C. or higher, 1170° C. or higher, 1180° C. or higher, 1185° C. or higher, 1190° C. or higher, 1195° C. or higher, and particularly 1200° C. or higher.


In the glass disk for a magnetic recording medium of the present invention, a Young's modulus is 78 GPa or higher, preferably 80 GPa or higher, 81 GPa or higher, 82 GPa or higher, and particularly preferably 83 GPa to 100 GPa. When the Young's modulus is too low, bending and flapping (fluttering) of the glass disk are likely to occur at the time of high-speed rotation, and thus an information recording medium and a magnetic head are likely to collide with each other.


The glass disk for a magnetic recording medium of the present invention preferably contains, as a glass composition, in terms of mol %, 60% to 71% of SiO2, 10% to 16% of Al2O3, 0% to 5% of B2O3, 0% to 0.1% of Na2O, 0% to 1% of K2O, 0% to 12% of MgO, 0% to 12% of CaO, 0% to 10% of SrO, 0% to 10% of BaO, 0% to 1% of ZrO2, and 0% to 1% of SnO2. Reasons for limiting a content range of each component as described above are shown below. In the description of the content range of each component, “%” means “mol %”.


When a content of SiO2 is too small, chemical resistance, particularly acid resistance, is likely to be decreased, and the strain point is likely to be decreased. On the other hand, when a content of SiO2 is too large, an etching rate with hydrofluoric acid or a mixed solution of hydrofluoric acid is likely to be decreased, the viscosity in high temperature is increased, meltability is likely to be decreased, and further, SiO2-based crystals, particularly cristobalite, are precipitated, and a liquidus viscosity is likely to be decreased. Therefore, an upper limit content of SiO2 is suitably 71%, 70.5%, 70%, 69.5%, 69%, 68.5%, 68%, and particularly 67.5%, and a lower limit content is suitably 60%, 61%, 62%, 62.5%, 63%, 63.5%, 64%, 64.5%, and particularly 65%. A most preferred content range is 66% to 70.5%.


When a content of Al2O3 is too small, the strain point is decreased, an amount of thermal shrinkage is increased, and the Young's modulus is decreased, so that the glass disk is likely to be bent. On the other hand, when a content of Al2O3 is too large, buffered hydrofluoric acid (BHF) resistance is decreased, a glass surface is likely to be clouded, and crack resistance is likely to be decreased. Further, SiO2—Al2O3-based crystals, particularly mullite, are precipitated in a glass, and the liquidus viscosity is likely to be decreased. An upper limit content of Al2O3 is suitably 16%, 15.5%, 15%, 14.5%, and particularly 14%, and a lower limit content is suitably 10%, 10.5%, 11%, 11.5%, and particularly 12%. A most preferred content range is 12% to 14%.


B2O3 is a component that acts as a flux, reduces a viscosity, and increases the meltability. When a content of B2O3 is too small, B2O3 does not sufficiently act as a flux, and the BHF resistance and the crack resistance are likely to be decreased. Further, a liquidus temperature is likely to rise. On the other hand, when a content of B2O3 is too large, the strain point, heat resistance, and the acid resistance are likely to be decreased, and particularly, the strain point is likely to be decreased. The glass is likely to be phase-separated. An upper limit content of B2O3 is suitably 5% and particularly 4.5%, and a lower limit content is suitably 0%, 1%, 1.5%, 2%, and particularly 2.5%. A most preferred content range is 2.5% to 4.5%.


Since alkali metal oxides (Li2O, Na2O, and K2O) deteriorate properties of a magnetic film formed on the glass disk, a content of each of the alkali metal oxides is preferably reduced to 0.1% (desirably 0.06%, 0.05%, 0.02%, and particularly 0.01%).


MgO is a component that decreases the viscosity in high temperature without decreasing the strain point and improves the meltability. In addition, MgO has an effect of decreasing a density most in RO, but when MgO is excessively introduced, the SiO2-based crystals, particularly the cristobalite, are precipitated, and the liquidus viscosity is likely to be decreased. Further, MgO is a component that easily reacts with BHF to form a product. The reaction product may be fixed or attached to the glass surface, which may make the glass cloudy. Further, impurities such as Fe2O3 may be mixed into the glass from a raw material for introducing MgO such as dolomite, and a transmittance of the glass disk may be reduced. Therefore, an upper limit content of MgO is suitably 12%, 11.5%, 11%, 10.5%, 10%, 9.5%, 9.3%, 9%, 8.5%, 8%, 7.5%, 7%, 6.5%, and particularly 6%, and a lower limit content is suitably 0%, 1%, 1.5%, 2%, 2.5%, 3%, 3.5%, 4%, and particularly 4.5%. A most preferred content range is 4.5% to 6%.


Similar to MgO, CaO is a component that decreases the viscosity in high temperature without decreasing the strain point and remarkably improves the meltability. However, when a content of CaO is too large, SiO2—Al2O3—RO-based crystals, particularly anorthite, are precipitated, the liquidus viscosity is likely to be decreased, the BHF resistance is decreased, and a reaction product is fixed or attached to the glass surface, which may make the glass cloudy. Therefore, an upper limit content of CaO is suitably 12%, 11.5%, 11%, 10.5%, 10%, 9.5%, 9%, and particularly 8.5%, and a lower limit content is suitably 0%, 1%, 2%, 3%, 3.5%, 4%, 4.5%, 5%, 5.5%, 5.6%, 6%, and particularly 6.5%. A most preferred content range is 6.5% to 8.5%.


SrO is a component that increases the chemical resistance and devitrification resistance, but when a ratio thereof is excessively increased in the entire RO, the meltability is likely to be decreased, and the density and a thermal expansion coefficient are likely to be increased. Therefore, a content of SrO is preferably 0% to 10%, 0% to 9%, 0% to 8%, 0% to 7%, 0% to 6%, and particularly 0% to 5%.


BaO is a component that increases the chemical resistance and the devitrification resistance, but when a content thereof is too large, the density is likely to be increased. A SiO2—Al2O3—B2O3—RO-based glass is generally difficult to melt, and thus it is very important to increase meltability and reduce a defective rate due to bubbles, foreign substances, and the like from a viewpoint of supplying a high-quality glass disk at a low cost and in a large amount. However, BaO has a poor effect of increasing the meltability in RO. Therefore, an upper limit content of BaO is suitably 10%, 9%, 8%, 7%, 6%, and particularly 5%, and a lower limit content thereof is suitably 0%, 0.1%, 0.3%, and particularly 0.2%.


SnO2 has a function as a fining agent for reducing bubbles in the glass. On the other hand, when a content of SnO2 is too large, devitrified crystals of SnO2 are likely to be generated in the glass. An upper limit content of SnO2 is suitably 1%, 0.5%, 0.4%, and particularly 0.3%, and a lower limit content is suitably 0%, 0.01%, 0.03%, and particularly 0.05%. A most preferred content range is 0.05% to 0.3%.


ZrO2 is a component that increases chemical durability, but when an introduction amount thereof is large, crystals of ZrSiO4 are likely to be generated. An upper limit content of ZrO2 is suitably 1%, 0.5%, 0.3%, 0.2%, and particularly 0.1%, and it is preferable to introduce ZrO2 in an amount of 0.001%% or more from a viewpoint of chemical durability. A most preferred content range is 0.001% to 0.1%. ZrO2 may be introduced from a raw material or may be introduced by extraction from a refractory.


In addition to the above components, other components may be introduced. An introduction amount thereof is preferably 5% or less, 3% or less, and particularly 1% or less.


ZnO is a component that improves the meltability and the BHF resistance, but when a content thereof is too large, the glass is likely to devitrify or the strain point is decreased, so that it is difficult to secure the heat resistance. Therefore, a content of ZnO is preferably 0% to 10%, 0% to 5%, 0% to 3%, 0% to 2%, and particularly 0% to 1%.


P2O5 is a component that decreases a liquidus temperature of SiO2—Al2O3—CaO-based crystals (particularly, anorthite) and SiO2—Al2O3-based crystals (particularly, mullite). However, when a large amount of P2O5 is introduced, the glass is likely to be phase-separated. Therefore, a content of P2O5 is preferably 0% to 10%, 0% to 5%, 0% to 3%, 0% to 2%, 0% to 1%, and particularly 0% to 0.1%.


TiO2 is a component that decreases the viscosity in high temperature and increases the meltability, and is a component that increases the chemical durability, but when TiO2 is excessively introduced, an ultraviolet transmittance is likely to be decreased. A content of TiO2 is preferably 3% or less, 1% or less, 0.5% or less, 0.1% or less, 0.05% or less, 0.03%, and particularly 0.01% or less. When a very small amount of TiO2 is introduced (for example, 0.0001% or more), an effect of preventing coloring due to ultraviolet rays is obtained. A most preferred content range is 0.0001% to 0.01%.


As2O3 and Sb2O3 are components that act as fining agents, but are environmentally hazardous chemical substances, and thus it is desirable not to use As2O3 and Sb2O3 as much as possible. A content of each of As2O3 and Sb2O3 is preferably less than 0.3%, less than 0.1%, less than 0.09%, less than 0.05%, less than 0.03%, less than 0.01%, less than 0.005%, and particularly less than 0.003%.


Fe is a component mixed from a raw material as an impurity, but when a content of Fe is too large, the ultraviolet transmittance may be decreased. Therefore, a lower limit content of Fe is suitably 0.0001%, 0.0005%, 0.001%, and particularly 0.0015% in terms of Fe2O3, and an upper limit content is suitably 0.01%, 0.009%, 0.008%, 0.007%, and particularly 0.006% in terms of Fe2O3. A most preferred content range is 0.0015% to 0.006%.


Cr2O3 is a component mixed from a raw material as an impurity, but when a content of Cr2O3 is too large, in a case of performing foreign substance inspection of an inside of the glass disk with scattered light, transmission of light is difficult to occur, and a failure may occur in the foreign substance inspection. Particularly, when a substrate size is 730 mm×920 mm or more, this failure is likely to occur. When a thickness of the glass disk is small (for example, 0.5 mm or less, 0.4 mm or less, and particularly 0.3 mm or less), an amount of scattered light is decreased, and thus it is more meaningful to regulate a content of Cr2O3. An upper limit content of Cr2O3 is suitably 0.001%, 0.0008%, 0.0006%, 0.0005%, and particularly 0.0003%, and a lower limit content is suitably 0.00001%. A most preferred content range is 0.00001% to 0.0003%.


SO3 is a component mixed from a raw material as an impurity, but when a content of SO3 is too large, bubbles called reboil may be generated during melting or forming, which may cause defects in the glass. An upper limit content of SO3 is suitably 0.005%, 0.003%, 0.002%, and particularly 0.001%, and a lower limit content is suitably 0.0001%. A most preferred content range is 0.0001% to 0.001%.


The glass disk for a magnetic recording medium of the present invention preferably has the following properties.


The glass disk for a magnetic recording medium is required to have an appropriate thermal expansion coefficient in order to enhance reliability of recording and reproduction of a magnetic recording medium. More specifically, a hard disk drive (HDD) incorporating the magnetic recording medium has a structure in which a central portion is pressed by a spindle of a spindle motor to rotate the magnetic recording medium itself. Therefore, when a difference in thermal expansion coefficient between the glass disk and a spindle material is too large, thermal expansion and thermal shrinkage of the glass disk and the spindle material are different from each other with respect to an ambient temperature change, and thus a phenomenon occurs in which the magnetic recording medium is deformed. When such a phenomenon occurs, written information cannot be read by a magnetic head, and the reliability of recording and reproduction may be impaired. Therefore, the glass disk for a magnetic recording medium desirably has a thermal expansion coefficient matching a thermal expansion coefficient of a spindle material (for example, stainless steel). From such a viewpoint, an average linear thermal expansion coefficient in a temperature range of 30° C. to 380° C. is preferably 25×10−7/° C. to 60×10−7/° C., 28×10−7/° C. to 55×10−7/° C., and particularly 30×10−7/° C. to 50×10−7/° C.


The liquidus temperature is preferably 1350° C. or lower, 1330° C. or lower, 1300° C. or lower, 1280° C. or lower, 1260° C. or lower, 1250° C. or lower, 1240° C. or lower, and particularly 1230° C. or lower. The liquidus viscosity is preferably 103.8 dPa·s or more, 104.4 dPa·s or more, 104.6 dPa·s or more, 104.8 dPa·s or more, and particularly 105.0 dPa·s or more. Accordingly, devitrified crystals are less likely to be precipitated at the time of forming, and the glass is easily formed into a sheet shape by an overflow down-draw method or the like, and thus the average surface roughness Ra of the surface can be made 1.0 nm or less and particularly 0.2 nm or less without polishing the surface or by polishing a small amount. As a result, magnetic properties can be increased with miniaturization of a bit size. The cost of the glass disk can be reduced by reducing the devitrified crystals or an amount of polishing. Here, the term “liquidus temperature” can be calculated by putting a glass powder that passes through a standard sieve of 30 mesh (500 μm) and remains on a sieve of 50 mesh (300 μm) into a platinum boat, holding the platinum boat in a temperature gradient furnace for 24 hours, and measuring a temperature at which crystals are precipitated. The term “liquidus viscosity” refers to a viscosity of a glass at a liquidus temperature, and can be measured by a platinum sphere pull up method.


An average linear transmittance in an optical path length of 1 mm and a wavelength range of 350 nm to 1500 nm is preferably 70% or more, 80% or more, and particularly 90% or more. When the average linear transmittance in the optical path length of 1 mm and the wavelength range of 350 nm to 1500 nm is too low, the magnetic layer is not sufficiently irradiated with laser light at the time of laser irradiation, and it is difficult to achieve a high Ku of the magnetic layer.


The β-OH is preferably 0.30/mm or less, 0.25/mm or less, 0.20/mm or less, 0.15/mm or less, and particularly 0.10/mm or less. When β-OH is too large, an annealing point is likely to be decreased. When β-OH is too small, it is highly necessary to introduce a dry component such as chlorine, and in that case, chlorine and the like in the glass remain in a high state, which may increase an environmental load. Therefore, β-OH is preferably 0.01/mm or more, and particularly 0.02/mm or more.


Examples of a method for reducing β-OH include the following methods. (1) A raw material having a low water content is selected. (2) A component (Cl, SO3, or the like) that reduces β-OH is added to the glass. (3) An amount of water in an atmosphere in a furnace is reduced. (4) N2 bubbling is performed in a molten glass. (5) A small melting furnace is adopted. (6) A flow rate of the molten glass is increased. (7) An electric melting method is adopted.


Here, the term “δ-OH” refers to a value obtained, using the following equation, by measuring a transmittance of the glass disk using FT-IR.





β-OH=(1/X)log(T1/T2)  [Equation 1]


X: thickness (mm)


T1: transmittance (%) at a reference wavelength of 3846 cm−1


T2: minimum transmittance (%) at a hydroxy group absorption wavelength of around 3600 cm−1


The average surface roughness Ra of the surface is preferably 1.0 nm or less, 0.7 nm or less, 0.4 nm or less, and particularly 0.2 nm or less. When the average surface roughness Ra of the surface is too large, improvement of the magnetic properties cannot be expected even if the bit size is miniaturized for a high recording density.


The thickness is preferably 1.5 mm or less, 1.2 mm or less, 0.2 mm to 1.0 mm, and particularly 0.3 mm to 0.9 mm. When the thickness is too large, polishing needs to be performed to a desired thickness, which may increase the processing cost.


A total thickness variation (TTV) is preferably less than 2.0 μm, 1.5 μm or less, 1.0 μm or less, and particularly 0.1 μm to less than 1.0 μm. When the total thickness variation (TTV) is too large, the improvement of the magnetic properties cannot be expected even if the bit size is miniaturized for the high recording density. Here, the term “total thickness variation (TTV)” is a difference between a maximum thickness and a minimum thickness of the entire glass disk, and can be measured by, for example, SBW-331ML/d manufactured by Kobelco Research Institute, Inc.


The entire surface of the glass disk for a magnetic recording medium of the present invention is preferably a polished surface. Accordingly, the total thickness variation (TTV) is likely to be regulated to less than 2.0 μm, 1.5 μm or less, 1.0 μm or less, and particularly less than 1.0 μm. As a method for a polishing treatment, various methods can be adopted, but a method of sandwiching both surfaces of the glass disk between a pair of polishing pads and performing the polishing treatment on the glass disk while rotating both the glass disk and the pair of polishing pads is preferred. Further, the pair of polishing pads preferably have different outer diameters, and the polishing treatment is preferably performed such that a part of the glass disk intermittently protrudes from the polishing pads at the time of polishing. Accordingly, the total thickness variation (TTV) is likely to be reduced, and an amount of warpage is also likely to be reduced. In the polishing treatment, a polishing depth is not particularly limited, and the polishing depth is preferably 50 μm or less, 30 μm or less, 20 μm or less, and particularly 10 μm or less. As the polishing depth is smaller, productivity of the glass disk is more improved.


The glass disk for a magnetic recording medium of the present invention can be produced, for example, by the following method. First, it is preferable that glass raw materials mixed so as to have a desired glass composition are put into a continuous melting furnace, heated and melted at 1500° C. to 1700° C., and fined, and then a molten glass is supplied to a forming device, formed into a sheet shape, and cooled. A known method can be adopted as a method of performing cutting into a disk shape after the forming into the sheet shape. As a method for forming a glass substrate, various methods can be adopted, and it is preferable to adopt an overflow down-draw method, a slot-down method, or the like in order to improve surface smoothness. It is possible to adopt, as appropriate, polishing of a disk surface for adjusting a thickness or TTV, drilling of a circular opening in a central portion of a disk, polishing of inner and outer peripheral end faces, forming of a magnetic layer on the disk surface, and the like.


Example 1

Hereinafter, the present invention will be described based on Examples. The following Examples are merely illustrative. The present invention is not limited to the following Examples.


Tables 1 to 5 show Examples (Samples Nos. 1 to 131) of the present invention.




















TABLE 1







No. 1
No. 2
No. 3
No. 4
No. 5
No. 6
No. 7
No. 8
No. 9
No. 10




























Glass
SiO2
mol %
67.32
67.97
67.34
64.92
64.87
64.75
65.86
65.80
65.87
66.80


composi-
Al2O3
mol %
12.57
12.70
12.27
13.93
13.97
14.14
13.98
14.02
14.05
13.00


tion
B2O3
mol %
3.00
3.00
2.80
3.98
3.99
4.04
3.01
3.02
3.05
3.05



Na2O
mol %
0.011
0.013
0.015
0.011
0.010
0.013
0.012
0.013
0.015
0.013



K2O
mol %
0.002
0.001
0.002
0.003
0.001
0.002
0.001
0.002
0.002
0.003



MgO
mol %
6.02
5.69
7.01
6.04
5.05
4.94
6.04
5.04
4.93
7.07



CaO
mol %
6.49
6.49
6.24
7.00
7.98
6.98
6.99
7.97
6.97
6.97



SrO
mol %
2.02
1.43
1.23
2.02
2.03
2.52
2.02
2.03
2.51
1.47



BaO
mol %
2.46
2.60
2.98
1.99
1.99
2.51
1.98
1.99
2.50
1.51



TiO2
mol %
0.003
0.003
0.003
0.002
0.003
0.003
0.003
0.004
0.002
0.001



ZrO2
mol %
0.003
0.005
0.011
0.005
0.003
0.004
0.005
0.008
0.010
0.011



SnO2
mol %
0.090
0.089
0.089
0.090
0.090
0.091
0.090
0.090
0.091
0.088



Fe2O3
mol %
0.004
0.004
0.003
0.004
0.005
0.005
0.004
0.004
0.004
0.004


















β-OH
/mm
0.15
0.15
0.14
0.18
0.18
0.18
0.15
0.15
0.15
0.15


Density
g/cm3
2.569
2.575
2.593
2.585
2.587
2.608
2.589
2.592
2.613
2.559


Thermal expansion
×10−7/
38.2
37.8
38.9
38.9
39.7
39.8
38.7
39.6
40.0
38.0


coefficient
° C.


Young's modulus
GPa
82.3
82.2
82.9
82.8
82.4
81.8
83.4
83.1
82.6
83.6


Strain point
° C.
722
725
719
717
716
715
726
727
726
723


Temperature at
° C.
1255
1260
1250
1226
1227
1231
1240
1240
1245
1243


104.5 dPa · s


Liquidus
° C.
1188
1191
1183
1177
1216
1205
1227
1247
1216
1199


temperature


Liquidus viscosity
dPa · s
5.2
5.2
5.2
5.0
4.6
4.8
4.6
4.5
4.8
4.9


(log η at TL)



























TABLE 2







No. 11
No. 12
No. 13
No. 14
No. 15
No. 16
No. 17
No. 18
No. 19
No. 20




























Glass
SiO2
mol %
66.88
66.80
66.92
66.77
66.76
67.87
67.72
67.76
67.94
64.89


composi-
Al2O3
mol %
13.04
13.00
13.00
13.02
13.01
12.02
12.02
11.98
11.98
13.97


tion
B2O3
mol %
2.96
3.00
2.97
3.00
3.03
3.00
3.03
3.04
2.97
3.98



Na2O
mol %
0.011
0.011
0.011
0.012
0.012
0.013
0.015
0.011
0.014
0.013



K2O
mol %
0.002
0.001
0.002
0.001
0.002
0.003
0.001
0.002
0.002
0.001



MgO
mol %
5.94
6.01
4.96
5.01
5.06
6.95
7.03
6.06
5.96
7.03



CaO
mol %
8.06
6.96
9.03
8.05
7.04
8.02
7.05
8.01
7.02
6.02



SrO
mol %
1.48
2.01
1.48
2.02
2.50
1.01
1.53
1.53
2.00
2.02



BaO
mol %
1.52
2.11
1.52
2.02
2.48
1.02
1.50
1.51
2.00
1.98



TiO2
mol %
0.004
0.003
0.003
0.002
0.003
0.002
0.002
0.001
0.002
0.001



ZrO2
mol %
0.016
0.011
0.014
0.010
0.006
0.006
0.007
0.006
0.007
0.008



SnO2
mol %
0.088
0.089
0.088
0.089
0.090
0.087
0.087
0.088
0.089
0.090



Fe2O3
mol %
0.004
0.004
0.005
0.005
0.005
0.005
0.006
0.005
0.004
0.004


















β-OH
/mm
0.15
0.15
0.15
0.15
0.15
0.15
0.15
0.15
0.15
0.18


Density
g/cm3
2.555
2.581
2.563
2.581
2.604
2.527
2.548
2.551
2.572
2.582


Thermal expansion
×10−7/
38.4
39.0
39.3
39.6
39.4
37.5
37.9
38.6
39.1
38.3


coefficient
° C.


Young's modulus
GPa
83.7
83.0
83.2
82.4
82.2
83.7
83.3
82.8
82.7
83.2


Strain point
° C.
722
721
721
720
720
717
716
717
715
718


Temperature at
° C.
1243
1246
1244
1247
1250
1245
1247
1247
1253
1227


104.5 dPa · s


Liquidus
° C.
1208
1210
1239
1216
1211
1258
1222
1221
1234
1193


temperature


Liquidus viscosity
dPa · s
4.8
4.9
4.6
4.8
4.9
4.5
4.7
4.7
4.7
4.8


(log η at TL)



























TABLE 3







No. 21
No. 22
No. 23
No. 24
No. 25
No. 26
No. 27
No. 28
No. 29
No. 30




























Glass
SiO2
mol %
64.90
64.88
65.75
65.80
65.85
65.76
65.86
66.83
66.86
66.80


composi-
Al2O3
mol %
14.10
14.01
14.03
14.01
13.99
13.02
14.01
12.98
13.01
13.99


tion
B2O3
mol %
3.93
4.05
3.00
3.04
2.98
3.01
3.99
4.03
3.97
3.01



Na2O
mol %
0.012
0.016
0.013
0.010
0.011
0.013
0.011
0.011
0.011
0.013



K2O
mol %
0.001
0.001
0.001
0.002
0.002
0.001
0.002
0.002
0.001
0.002



MgO
mol %
5.95
5.96
7.03
5.93
4.98
7.05
6.05
5.97
6.01
6.04



CaO
mol %
5.98
6.98
6.02
6.09
6.05
6.04
6.04
7.03
6.00
6.03



SrO
mol %
2.51
0.00
2.02
2.51
3.01
2.48
1.96
1.03
2.01
2.02



BaO
mol %
2.50
3.99
2.02
2.50
3.02
2.52
1.99
2.01
2.02
1.98



TiO2
mol %
0.003
0.002
0.003
0.004
0.003
0.003
0.003
0.003
0.003
0.003



ZrO2
mol %
0.010
0.013
0.013
0.011
0.006
0.005
0.011
0.005
0.003
0.004



SnO2
mol %
0.091
0.091
0.090
0.091
0.092
0.090
0.090
0.089
0.089
0.090



Fe2O3
mol %
0.004
0.005
0.005
0.005
0.004
0.004
0.003
0.004
0.005
0.005


















β-OH
/mm
0.18
0.18
0.15
0.15
0.14
0.15
0.18
0.18
0.18
0.15


Density
g/cm3
2.603
2.609
2.586
2.610
2.633
2.612
2.571
2.549
2.564
2.576


Thermal expansion
×10−7/
39.3
39.0
38.2
39.3
40.4
40.1
37.6
37.4
37.8
37.4


coefficient
° C.


Young's modulus
GPa
82.3
81.7
84.1
83.1
82.4
83.2
82.4
81.9
81.7
83.5


Strain point
° C.
716
715
727
726
725
717
721
715
715
729


Temperature at
° C.
1232
1228
1241
1247
1250
1235
1242
1241
1246
1261


104.5 dPa · s


Liquidus
° C.
1200
1186
1200
1205
1191
1222
1195
1223
1213
1219


temperature


Liquidus viscosity
dPa · s
4.8
4.9
4.9
4.9
5.1
4.6
5.0
4.7
4.8
4.9


(log η at TL)



























TABLE 4







No. 31
No. 32
No. 33
No. 34
No. 35
No. 36
No. 37
No. 38
No. 39
No. 40




























Glass
SiO2
mol %
64.87
66.15
65.77
66.80
66.79
66.22
66.88
66.64
67.87
66.77


composi-
Al2O3
mol %
13.99
13.84
14.00
14.03
14.00
14.51
14.03
14.04
12.99
14.03


tion
B2O3
mol %
4.04
3.96
4.00
2.99
3.01
3.02
2.99
3.03
2.99
2.96



Na2O
mol %
0.012
0.013
0.011
0.013
0.011
0.011
0.011
0.012
0.011
0.013



K2O
mol %
0.001
0.002
0.002
0.003
0.002
0.001
0.002
0.001
0.002
0.003



MgO
mol %
6.97
6.00
6.07
6.00
6.04
6.06
6.00
6.09
6.00
5.12



CaO
mol %
5.99
6.95
6.06
7.07
6.03
6.05
5.99
6.08
5.99
6.01



SrO
mol %
0.00
0.97
1.51
0.97
2.02
2.03
2.98
0.99
2.01
1.99



BaO
mol %
4.02
2.02
2.48
2.02
1.98
1.99
1.01
3.02
2.02
3.00



TiO2
mol %
0.003
0.004
0.002
0.003
0.004
0.003
0.003
0.002
0.003
0.003



ZrO2
mol %
0.006
0.008
0.010
0.011
0.016
0.011
0.014
0.010
0.005
0.007



SnO2
mol %
0.091
0.089
0.090
0.089
0.090
0.090
0.089
0.090
0.089
0.091



Fe2O3
mol %
0.004
0.004
0.004
0.004
0.004
0.004
0.005
0.005
0.005
0.006


















β-OH
/mm
0.18
0.18
0.18
0.15
0.15
0.15
0.15
0.15
0.15
0.14


Density
g/cm3
2.608
2.557
2.577
2.563
2.576
2.581
2.563
2.589
2.567
2.606


Thermal expansion
×10−7/
38.6
37.2
37.7
37.2
37.2
37.0
37.1
37.2
37.3
38.5


coefficient
° C.


Young's modulus
GPa
82.9
83.1
82.8
84.0
83.6
84.1
83.9
83.3
82.8
82.6


Strain point
° C.
716
719
719
730
731
733
733
733
727
730


Temperature at
° C.
1230
1235
1238
1252
1254
1251
1253
1258
1260
1259


104.5 dPa · s


Liquidus
° C.
1207
1192
1189
1221
1202
1239
1214
1208
1188
1204


temperature


Liquidus viscosity
dPa · s
4.7
4.9
5.0
4.8
5.0
4.6
4.9
5.0
5.2
5.0


(log η at TL)



























TABLE 5







No. 41
No. 42
No. 43
No. 44
No. 45
No. 46
No. 47
No. 48
No. 49
No. 50




























Glass
SiO2
mol %
67.14
67.65
67.78
66.85
67.06
67.33
67.21
67.37
67.88
67.88


composi-
Al2O3
mol %
12.18
13.03
13.01
13.03
13.47
13.02
12.19
12.59
12.70
13.00


tion
B2O3
mol %
2.91
3.03
2.93
4.05
2.93
2.93
2.86
2.99
3.00
3.00



Na2O
mol %
0.011
0.011
0.014
0.013
0.012
0.011
0.013
0.010
0.011
0.011



K2O
mol %
0.001
0.002
0.002
0.001
0.001
0.001
0.001
0.002
0.002
0.002



MgO
mol %
6.87
5.07
5.57
5.99
5.57
5.06
6.93
6.00
6.00
5.70



CaO
mol %
6.26
6.56
6.55
6.46
6.55
6.55
7.23
6.59
6.30
6.30



SrO
mol %
1.30
1.51
0.53
1.49
1.51
2.50
1.28
2.33
1.70
1.40



BaO
mol %
3.21
3.02
3.51
2.01
2.79
2.49
2.17
2.02
2.30
2.60



TiO2
mol %
0.002
0.003
0.002
0.003
0.003
0.002
0.003
0.003
0.003
0.003



ZrO2
mol %
0.008
0.007
0.007
0.008
0.010
0.013
0.013
0.011
0.005
0.005



SnO2
mol %
0.090
0.090
0.090
0.089
0.090
0.090
0.088
0.089
0.089
0.090



Fe2O3
mol %
0.006
0.005
0.004
0.004
0.004
0.005
0.005
0.005
0.004
0.004


















β-OH
/mm
0.14
0.15
0.14
0.18
0.14
0.14
0.14
0.15
0.15
0.15


Density
g/cm3
2.596
2.590
2.588
2.554
2.592
2.619
2.574
2.561
2.572
2.569


Thermal expansion
×10−7/
38.8
38.5
38.1
37.5
38.4
40.4
39.1
37.7
38.1
37.3


coefficient
° C.


Young's modulus
GPa
82.4
82.0
82.1
82.1
82.9
82.0
83.4
82.4
82.5
81.7


Strain point
° C.
718
726
727
717
728
721
717
726
723
728


Temperature at
° C.
1250
1263
1262
1244
1256
1251
1241
1258
1256
1266


104.5 dPa · s


Liquidus
° C.
1158
1202
1181
1173
1200
1227
1192
1201
1196
1207


temperature


Liquidus viscosity
dPa · s
5.4
5.1
5.3
5.2
5.1
4.7
5.0
5.1
5.1
5.1


(log η at TL)



























TABLE 6







No. 51
No. 52
No. 53
No. 54
No. 55
No. 56
No. 57
No. 58
No. 59
No. 60




























Glass
SiO2
mol %
67.52
65.92
65.78
65.96
65.74
66.00
65.80
66.04
65.68
65.88


composi-
Al2O3
mol %
13.11
14.93
14.90
14.95
14.99
14.84
14.98
14.86
15.17
14.97


tion
B2O3
mol %
3.30
2.03
2.15
1.96
2.09
2.01
2.09
2.02
2.03
1.96



Na2O
mol %
0.007
0.020
0.020
0.013
0.016
0.023
0.014
0.016
0.015
0.020



K2O
mol %
0.000
0.003
0.002
0.002
0.001
0.002
0.002
0.001
0.002
0.002



MgO
mol %
6.16
6.94
6.95
6.97
6.97
6.94
7.96
7.92
7.94
7.98



CaO
mol %
6.50
6.05
6.10
4.06
4.10
4.10
6.04
6.05
4.05
4.08



SrO
mol %
1.59
3.01
1.01
4.99
3.01
1.01
3.00
1.02
4.98
3.02



BaO
mol %
1.69
0.99
2.98
1.00
2.99
4.98
0.03
1.97
0.04
2.00



TiO2
mol %
0.003
0.007
0.007
0.006
0.007
0.009
0.007
0.007
0.006
0.007



ZrO2
mol %
0.010
0.001
0.001
0.001
0.001
0.002
0.001
0.001
0.001
0.001



SnO2
mol %
0.096
0.080
0.086
0.082
0.087
0.084
0.079
0.085
0.080
0.086



Fe2O3
mol %
0.003
0.007
0.007
0.007
0.006
0.007
0.007
0.007
0.007
0.007


















β-OH
/mm
0.10
0.14
0.14
0.14
0.15
0.15
0.15
0.13
0.13
0.15


Density
g/cm3
2.549
2.586
2.614
2.616
2.644
2.669
2.558
2.583
2.590
2.613


Thermal expansion
×10−7/
37.1
37.6
37.9
38.1
38.4
38.7
36.4
36.7
36.9
37.2


coefficient
° C.


Young's modulus
GPa
83.0
85.7
85.1
85.2
84.4
83.7
86.9
86.2
86.6
85.6


Strain point
° C.
725
741
740
741
740
740
741
741
742
740


Temperature at
° C.
1255
1247
1250
1250
1255
1255
1241
1242
1249
1249


104.5 dPa · s


Liquidus
° C.
1184
1265
1256
1269
1253
1227
1295
1282
1294
1285


temperature


Liquidus viscosity
dPa · s
5.2
4.3
4.5
4.3
4.5
4.8
4.0
4.1
4.1
4.2


(log η at TL)



























TABLE 7







No. 61
No. 62
No. 63
No. 64
No. 65
No. 66
No. 67
No. 68
No. 69
No. 70




























Glass
SiO2
mol %
65.85
66.01
66.01
66.90
66.90
68.68
68.79
68.76
68.83
68.86


composi-
Al2O3
mol %
14.87
13.97
13.99
13.97
14.02
13.60
13.53
13.53
13.57
13.53


tion
B2O3
mol %
2.08
1.92
1.92
1.92
0.96
1.11
1.03
1.05
0.86
0.97



Na2O
mol %
0.018
0.027
0.017
0.015
0.015
0.017
0.014
0.016
0.014
0.012



K2O
mol %
0.001
0.002
0.001
0.001
0.001
0.001
0.001
0.001
0.001
0.001



MgO
mol %
7.97
6.95
7.94
7.04
6.94
6.96
6.96
6.98
6.99
6.98



CaO
mol %
4.11
7.01
6.03
6.04
7.04
9.00
7.02
7.06
5.05
5.05



SrO
mol %
1.02
3.00
3.00
3.01
3.02
0.52
2.52
0.51
4.52
2.51



BaO
mol %
3.98
1.00
1.00
1.00
1.00
0.00
0.03
1.99
0.06
2.00



TiO2
mol %
0.007
0.006
0.006
0.006
0.006
0.010
0.009
0.007
0.007
0.008



ZrO2
mol %
0.001
0.001
0.001
0.001
0.001
0.002
0.001
0.001
0.001
0.001



SnO2
mol %
0.087
0.080
0.080
0.080
0.093
0.086
0.082
0.088
0.084
0.085



Fe2O3
mol %
0.007
0.007
0.007
0.007
0.007
0.008
0.008
0.007
0.007
0.007


















β-OH
/mm
0.13
0.13
0.14
0.14
0.14
0.15
0.15
0.15
0.14
0.14


Density
g/cm3
2.640
2.590
2.588
2.579
2.597
2.507
2.538
2.564
2.569
2.592


Thermal expansion
×10−7/
37.5
39.4
38.6
37.8
39.2
35.8
36.3
36.6
36.8
37.1


coefficient
° C.


Young's modulus
GPa
84.9
85.5
86.0
85.3
86.5
86.9
86.3
85.5
85.7
85.1


Strain point
° C.
740
733
733
737
744
753
750
750
750
749


Temperature at
° C.
1254
1239
1239
1250
1253
1268
1273
1277
1279
1283


104.5 dPa · s


Liquidus
° C.
1282
1243
1245
1222
1266
1282
1263
1273
1259
1262


temperature


Liquidus viscosity
dPa · s
4.2
4.5
4.5
4.8
4.4
4.4
4.6
4.5
4.7
4.7


(log η at TL)



























TABLE 8







No. 71
No. 72
No. 73
No. 74
No. 75
No. 76
No. 77
No. 78
No. 79
No. 80




























Glass
SiO2
mol %
68.75
68.07
67.75
67.77
68.06
67.90
67.84
66.83
67.35
66.96


composi-
Al2O3
mol %
13.55
13.41
13.57
13.55
13.50
13.49
13.51
13.37
13.36
13.44


tion
B2O3
mol %
0.98
1.11
1.03
1.04
0.86
0.96
0.98
3.26
2.78
3.57



Na2O
mol %
0.012
0.015
0.015
0.013
0.015
0.013
0.012
0.020
0.017
0.030



K2O
mol %
0.001
0.001
0.001
0.001
0.001
0.001
0.001
0.002
0.002
0.002



MgO
mol %
6.96
7.84
7.96
7.95
7.91
7.94
7.93
6.37
6.35
5.87



CaO
mol %
5.11
8.93
7.02
7.05
5.03
5.06
5.11
6.54
6.54
6.54



SrO
mol %
0.52
0.51
2.52
0.51
4.47
2.53
0.51
1.81
1.81
1.61



BaO
mol %
4.02
0.01
0.03
2.00
0.06
2.00
4.01
1.70
1.70
1.90



TiO2
mol %
0.009
0.007
0.007
0.007
0.007
0.008
0.009
0.006
0.006
0.006



ZrO2
mol %
0.001
0.001
0.001
0.001
0.001
0.001
0.001
0.001
0.001
0.001



SnO2
mol %
0.086
0.081
0.082
0.088
0.083
0.085
0.086
0.080
0.075
0.076



Fe2O3
mol %
0.007
0.008
0.008
0.007
0.007
0.008
0.007
0.008
0.007
0.007


















β-OH
/mm
0.14
0.15
0.15
0.15
0.13
0.13
0.15
0.15
0.15
0.14


Density
g/cm3
2.620
2.518
2.548
2.574
2.580
2.604
2.631
2.562
2.565
2.559


Thermal expansion
×10−7/
37.4
36.6
37.1
37.4
37.6
37.9
38.2
37.6
37.5
37.3


coefficient
° C.


Young's modulus
GPa
84.5
87.7
87.2
86.5
86.5
85.8
85.1
83.5
84.0
82.9


Strain point
° C.
750
747
747
745
747
745
746
724
730
723


Temperature at
° C.
1287
1254
1257
1261
1259
1273
1271
1247
1256
1252


104.5 dPa · s


Liquidus
° C.
1262.0
1255
1243
1280
1273
1267
1278
1202
1207
1190


temperature


Liquidus viscosity
dPa · s
4.7
4.5
4.6
4.3
4.4
4.5
4.4
4.9
5.0
5.1


(log η at TL)



























TABLE 9







No. 81
No. 82
No. 83
No. 84
No. 85
No. 86
No. 87
No. 88
No. 89
No. 90




























Glass
SiO2
mol %
67.22
67.59
67.61
67.28
67.59
67.55
67.60
67.54
67.63
67.29


composi-
Al2O3
mol %
13.42
12.62
12.85
13.78
13.73
13.53
13.71
13.52
13.50
13.54


tion
B2O3
mol %
3.28
3.16
3.06
1.52
1.51
1.51
1.51
1.50
1.41
1.50



Na2O
mol %
0.024
0.027
0.016
0.030
0.024
0.023
0.020
0.032
0.020
0.018



K2O
mol %
0.004
0.004
0.002
0.005
0.004
0.005
0.004
0.003
0.003
0.003



MgO
mol %
5.74
6.45
6.45
7.53
7.53
75.3
7.52
7.52
7.80
7.79



CaO
mol %
6.64
6.54
6.63
6.52
6.52
6.52
6.52
7.00
7.01
7.01



SrO
mol %
1.61
1.51
1.60
2.76
2.75
2.99
3.00
2.74
2.50
2.49



BaO
mol %
1.89
2.00
1.70
0.50
0.25
0.25
0.03
0.03
0.03
0.25



TiO2
mol %
0.007
0.007
0.007
0.007
0.007
0.006
0.007
0.007
0.017
0.007



ZrO2
mol %
0.001
0.001
0.001
0.001
0.001
0.001
0.001
0.001
0.001
0.001



SnO2
mol %
0.080
0.075
0.079
0.079
0.078
0.078
0.078
0.078
0.078
0.082



Fe2O3
mol %
0.071
0.007
0.007
0.007
0.007
0.008
0.008
0.008
0.008
0.008


















β-OH
/mm
0.14
0.14
0.14
0.14
0.15
0.15
0.15
0.14
0.14
0.14


Density
g/cm3
2.560
2.559
2.555
2.563
2.554
2.558
2.551
2.548
2.544
2.554


Thermal expansion
×10−7/
37.3
37.9
37.6
37.5
37.0
37.5
37.0
37.4
37.1
37.6


coefficient
° C.


Young's modulus
GPa
83.1
82.4
83.0
86.2
86.4
86.2
86.6
86.5
86.6
86.6


Strain point
° C.
726
719
724
739
741
738
741
738
739
738


Temperature at
° C.
1256
1250
1252
1254
1257
1256
1255
1255
1253
1251


104.5 dPa · s


Liquidus
° C.
1200
1184
1196
1240
1255
1240
1246
1239
1247
1246


temperature


Liquidus viscosity
dPa · s
5.0
5.2
5.1
4.6
4.5
4.7
4.6
4.7
4.6
4.6


(log η at TL)



























TABLE 10







No. 91
No. 92
No. 93
No. 94
No. 95
No. 96
No. 97
No. 98
No. 99
No. 100




























Glass
SiO2
mol %
67.63
67.49
67.50
67.48
67.33
67.64
67.81
67.62
67.72
67.33


composi-
Al2O3
mol %
13.52
13.38
13.35
13.37
13.37
13.35
12.75
12.87
12.85
13.39


tion
B2O3
mol %
1.41
3.17
3.17
3.21
3.19
3.21
3.21
3.23
3.18
3.17



Na2O
mol %
0.016
0.015
0.015
0.014
0.014
0.014
0.014
0.013
0.014
0.014



K2O
mol %
0.003
0.001
0.001
0.001
0.001
0.001
0.001
0.001
0.001
0.001



MgO
mol %
7.54
5.67
5.75
5.85
5.86
5.63
6.34
6.33
6.34
6.14



CaO
mol %
6.78
6.55
6.59
6.55
6.60
6.53
6.56
6.53
6.57
6.52



SrO
mol %
2.76
1.62
1.52
1.62
1.63
1.62
1.42
1.52
1.42
1.63



BaO
mol %
0.25
2.01
2.01
1.81
1.91
1.91
1.80
1.80
1.81
1.71



TiO2
mol %
0.01
0.01
0.01
0.01
0.01
0.01
0.01
0.01
0.01
0.01



ZrO2
mol %
0.00
0.00
0.00
0.00
0.00
0.00
0.00
0.00
0.00
0.00



SnO2
mol %
0.08
0.08
0.08
0.08
0.08
0.08
0.08
0.08
0.08
0.08



Fe2O3
mol %
0.01
0.01
0.01
0.01
0.01
0.01
0.01
0.01
0.01
0.01


















β-OH
/mm
0.15
0.15
0.15
0.13
0.13
0.15
0.13
0.13
0.14
0.14


Density
g/cm3
2.555
2.561
2.559
2.555
2.559
2.556
2.549
2.552
2.550
2.552


Thermal expansion
×10−7/
37.5
37.3
37.2
37.1
37.3
37.1
37.2
37.4
37.2
37.1


coefficient
° C.


Young's modulus
GPa
86.4
82.5
82.7
82.9
82.7
82.5
82.6
82.8
82.8
83.2


Strain point
° C.
738
724
724
725
723
725
721
721
720
725


Temperature at
° C.
1255
1259
1257
1256
1255
1257
1255
1252
1253
1255


104.5 dPa · s


Liquidus
° C.
1228
1199
1199
1198
1191
1201
1191
1196
1180
1212


temperature


Liquidus viscosity
dPa · s
4.8
5.1
5.1
5.1
5.1
5.1
5.1
5.1
5.2
4.9


(log η at TL)



























TABLE 11







No. 101
No. 102
No. 103
No. 104
No. 105
No. 106
No. 107
No. 108
No. 109
No. 110




























Glass
SiO2
mol %
67.40
67.67
67.83
67.99
67.87
68.52
68.45
67.88
67.87
67.95


composi-
Al2O3
mol %
13.08
13.33
13.35
13.50
13.49
13.50
13.50
13.50
13.42
13.51


tion
B2O3
mol %
3.15
3.25
3.25
1.10
1.10
1.10
1.60
1.08
1.16
1.56



Na2O
mol %
0.014
0.018
0.015
0.017
0.012
0.017
0.013
0.031
0.018
0.017



K2O
mol %
0.001
0.003
0.004
0.007
0.001
0.007
0.001
0.007
0.003
0.003



MgO
mol %
6.35
5.65
5.44
7.94
8.05
7.42
7.46
7.96
7.97
7.50



CaO
mol %
6.56
6.55
6.57
8.94
8.96
8.93
8.46
9.04
9.06
8.94



SrO
mol %
1.63
1.62
1.63
0.41
0.41
0.41
0.41
0.41
0.41
0.41



BaO
mol %
1.70
1.80
1.80
0.00
0.00
0.00
0.00
0.00
0.00
0.01



TiO2
mol %
0.007
0.007
0.006
0.008
0.007
0.008
0.008
0.007
0.007
0.007



ZrO2
mol %
0.001
0.001
0.001
0.002
0.001
0.001
0.001
0.001
0.001
0.001



SnO2
mol %
0.089
0.089
0.089
0.081
0.081
0.077
0.081
0.081
0.077
0.081



Fe2O3
mol %
0.007
0.007
0.007
0.009
0.009
0.009
0.008
0.009
0.009
0.009


















β-OH
/mm
0.14
0.15
0.15
0.15
0.14
0.14
0.14
0.15
0.15
0.15


Density
g/cm3
2.553
2.552
2.551
2.515
2.516
2.509
2.500
2.515
2.514
2.507


Thermal expansion
×10−7/
37.3
36.9
36.8
36.4
36.5
36.0
35.4
36.6
36.6
36.2


coefficient
° C.


Young's modulus
GPa
83.0
82.8
82.6
87.8
87.9
87.5
87.0
87.6
87.6
87.1


Strain point
° C.
722
723
725
747
747
749
746
747
745
743


Temperature at
° C.
1249
1258
1263
1254
1254
1263
1262
1254
1253
1256


104.5 dPa · s


Liquidus
° C.
1194
1198
1181
1261
1265
1263
1257
1253
1255
1247


temperature


Liquidus viscosity
dPa · s
5.0
5.1
5.3
4.4
4.4
4.5
4.6
4.5
4.5
4.6


(log η at TL)



























TABLE 12







No. 111
No. 112
No. 113
No. 114
No. 115
No. 116
No. 117
No. 118
No. 119
No. 120




























Glass
SiO2
mol %
68.15
70.34
68.79
68.72
67.27
67.29
67.33
65.79
65.81
68.78


composi-
Al2O3
mol %
13.32
13.48
13.47
13.54
13.47
13.47
13.48
13.47
13.47
12.50


tion
B2O3
mol %
1.57
0.00
0.00
0.00
0.00
0.00
0.00
0.00
0.00
0.00



Na2O
mol %
0.021
0.010
0.010
0.010
0.010
0.010
0.010
0.010
0.010
0.010



K2O
mol %
0.003
0.002
0.002
0.001
0.001
0.001
0.001
0.001
0.001
0.001



MgO
mol %
7.47
7.52
9.07
7.57
10.60
9.06
7.52
10.58
9.07
9.53



CaO
mol %
8.96
8.03
8.04
9.55
8.05
9.55
11.04
9.54
11.04
8.56



SrO
mol %
0.41
0.51
0.51
0.51
0.50
0.51
0.51
0.50
0.51
0.51



BaO
mol %
0.00
0.01
0.01
0.00
0.00
0.01
0.00
0.00
0.00
0.01



TiO2
mol %
0.008
0.006
0.007
0.006
0.006
0.007
0.007
0.006
0.006
0.007



ZrO2
mol %
0.001
0.001
0.001
0.001
0.001
0.001
0.001
0.001
0.001
0.001



SnO2
mol %
0.077
0.085
0.081
0.085
0.084
0.085
0.085
0.080
0.081
0.080



Fe2O3
mol %
0.009
0.008
0.009
0.008
0.009
0.009
0.009
0.010
0.009
0.010


















β-OH
/mm
0.13
0.13
0.15
0.15
0.15
0.14
0.14
0.14
0.14
0.15


Density
g/cm3
2.505
2.505
2.521
2.525
2.537
2.541
2.544
2.557
2.561
2.523


Thermal expansion
×10−7/
36.2
34.4
35.6
36.8
36.8
38.0
39.2
39.2
40.4
37.6


coefficient
° C.


Young's modulus
GPa
86.8
88.0
89.1
88.4
90.3
89.4
88.7
90.5
90.0
88.7


Strain point
° C.
743
767
761
762
754
756
757
750
750
753


Temperature at
° C.
1258
1289
1268
1268
1246
1247
1249
1228
1228
1261


104.5 dPa · s


Liquidus
° C.
1241
1283
1288
1270
1289
1265
1293
1260
1285
1262


temperature


Liquidus viscosity
dPa · s
4.7
4.6
4.3
4.5
4.1
4.3
4.1
4.2
4.0
4.5


(log η at TL)
























TABLE 13










No. 121
No. 122
No. 123
No. 124
No. 125
No. 126





Glass
SiO2
mol %
68.81
67.29
67.30
67.25
65.83
65.86


composition
Al2O3
mol %
12.50
12.50
12.50
12.55
12.48
12.48



B2O3
mol %
0.00
0.00
0.00
0.00
0.00
0.00



Na2O
mol %
0.010
0.010
0.010
0.010
0.010
0.010



K2O
mol %
0.001
0.001
0.001
0.001
0.001
0.001



MgO
mol %
8.03
11.03
9.55
8.00
11.00
9.52



CaO
mol %
10.04
8.56
10.03
11.57
10.06
11.52



SrO
mol %
0.51
0.51
0.51
0.51
0.50
0.51



BaO
mol %
0.00
0.01
0.00
0.00
0.01
0.00



TiO2
mol %
0.007
0.007
0.007
0.007
0.007
0.006



ZrO2
mol %
0.001
0.001
0.001
0.001
0.001
0.001



SnO2
mol %
0.085
0.080
0.084
0.084
0.084
0.084



Fe2O3
mol %
0.010
0.011
0.009
0.010
0.010
0.010














β-OH
/mm
0.15
0.13
0.13
0.15
0.13
0.13


Density
g/cm3
2.527
2.540
2.544
2.548
2.561
2.565


Thermal expansion
×10−7/
38.7
38.7
39.9
41.1
41.1
42.3


coefficient
° C.


Young's modulus
GPa
88.1
89.7
89.1
88.4
90.2
89.5


Strain point
° C.
754
748
747
746
740
738


Temperature at
° C.
1262
1243
1242
1238
1220
1222


104.5 dPa · s


Liquidus
° C.
1268
1250
1251
1273
1241
1260


temperature


Liquidus viscosity
dPa · s
4.5
4.4
4.4
4.2
4.3
4.1


(log η at TL)






















No. 127
No. 128
No. 129
No. 130
No. 131







Glass
SiO2
mol %
68.75
68.76
67.24
67.29
65.79



composition
Al2O3
mol %
14.54
14.54
14.53
14.52
14.52




B2O3
mol %
0.00
0.00
0.00
0.00
0.00




Na2O
mol %
0.010
0.010
0.010
0.010
0.010




K2O
mol %
0.001
0.001
0.001
0.001
0.001




MgO
mol %
8.52
7.00
10.04
8.51
10.01




CaO
mol %
7.56
9.05
7.56
9.05
9.05




SrO
mol %
0.51
0.52
0.51
0.51
0.51




BaO
mol %
0.00
0.01
0.01
0.00
0.00




TiO2
mol %
0.007
0.007
0.007
0.007
0.007




ZrO2
mol %
0.001
0.001
0.001
0.001
0.001




SnO2
mol %
0.086
0.086
0.081
0.085
0.081




Fe2O3
mol %
0.008
0.009
0.010
0.009
0.009















β-OH
/mm
0.14
0.13
0.15
0.13
0.13



Density
g/cm3
2.520
2.523
2.535
2.539
2.555



Thermal expansion
×10−7/
34.8
36.0
36.0
37.2
38.4



coefficient
° C.



Young's modulus
GPa
89.5
88.8
90.6
90.0
91.0



Strain point
° C.
767
769
761
761
754



Temperature at
° C.
1273
1278
1254
1256
1236



104.5 dPa · s



Liquidus
° C.
1316
1280
1321
1286
1289



temperature



Liquidus viscosity
dPa · s
4.1
4.5
3.9
4.2
4.0



(log η at TL)










Each sample was prepared as follows. First, a glass batch obtained by mixing glass raw materials so as to have a glass composition shown in the tables was put into a platinum crucible and melted at 1600° C. for 24 hours. When melting the glass batch, the glass batch was stirred using a platinum stirrer for homogenization. Next, the molten glass was poured onto a carbon sheet, formed into a flat sheet shape, and then cut into a disk shape. For each of the obtained samples, a β-OH value, a density, a thermal expansion coefficient, a Young's modulus, a strain point, a temperature at 104.5 dPa·s, a liquidus temperature, a liquidus viscosity, and a thermal shrinkage were evaluated.


The β-OH value is a value calculated by the above equation.


The density is a value measured by a known Archimedes method.


The thermal expansion coefficient is an average thermal expansion coefficient measured with a dilatometer in a temperature range of 30° C. to 380° C.


The Young's modulus is a value measured by a dynamic elastic modulus measurement method (a resonance method) based on JIS R1602.


The strain point is a value measured based on a method of ASTM C336.


The temperature at a viscosity in high temperature of 104.5 dPa·s is a value measured by a platinum sphere pull up method.


The liquidus temperature is a temperature at which each sample is grinded, a glass powder that passes through a standard sieve of 30 mesh (500 μm) and remains on a sieve of 50 mesh (300 μm) is put into a platinum boat, the platinum boat is held in a temperature gradient furnace set at 1100° C. to 1350° C. for 24 hours, then the platinum boat is taken out, and devitrified crystals (crystal foreign substances) are observed in a glass. The liquidus viscosity is a value obtained by measuring a viscosity of a glass at a liquidus temperature by a platinum sphere pull up method.


As is clear from the tables, Sample Nos. 1 to 131 have a strain point of 715° C. or higher, a temperature at 104.5 dPa·s of 1290° C. or lower, and a Young's modulus of 81.7 GPa or higher, and thus are suitable as a glass disk for a magnetic recording medium.


A glass batch obtained by mixing glass raw materials so as to have a glass composition of each of Sample Nos. 1 to 131 in the tables was put into a melting kiln, melted at 1500° C. to 1700° C. for 24 hours, fined, homogenized, formed into a sheet shape by an overflow down-draw method so as to have a thickness of 0.675 mm, and then processed into a disk shape. A surface roughness Ra of a surface of the obtained glass disk was measured by an atomic force microscope (AFM) and found to be 0.10 nm to 0.20 nm. A total thickness variation (TTV) was 1.0 μm. Further, an average linear transmittance of the obtained glass disk in an optical path length of 1 mm and a wavelength range of 350 nm to 1500 nm was measured with a spectrophotometer UV-3100 manufactured by Shimadzu Corporation, and found to be 85% or more in each case.

Claims
  • 1. A glass disk for a magnetic recording medium, wherein the glass disk has a disk shape, and has a strain point of 695° C. to 780° C., a temperature at 104.5 dPa·s of 1300° C. or lower, and a Young's modulus of 78 GPa or higher.
  • 2. The glass disk for a magnetic recording medium according to claim 1, wherein a circular opening is formed in a central portion of the glass disk.
  • 3. The glass disk for a magnetic recording medium according to claim 1, wherein the glass disk contains, as a glass composition, in terms of mol %, 60% to 71% of SiO2, 10% to 16% of Al2O3, 0% to 5% of B2O3, 0% to 0.1% of Na2O, 0% to 1% of K2O, 0% to 12% of MgO, 0% to 12% of CaO, 0% to 10% of SrO, 0% to 10% of BaO, 0% to 1% of ZrO2, and 0% to 1% of SnO2.
  • 4. The glass disk for a magnetic recording medium according to claim 1, wherein an average surface roughness Ra of a surface of the glass disk is 1.0 nm or less.
  • 5. The glass disk for a magnetic recording medium according to claim 1, wherein an average linear transmittance in an optical path length of 1 mm and a wavelength range of 350 nm to 1500 nm is 70% or more.
  • 6. A glass disk for a magnetic recording medium, wherein the glass disk has a disk shape, and contains, as a glass composition, in terms of mol %, 60% to 71% of SiO2, 10% to 16% of Al2O3, 0% to 5% of B2O3, 0% to 0.1% of Na2O, 0% to 1% of K2O, 0% to 12% of MgO, 0% to 12% of CaO, 0% to 10% of SrO, 0% to 10% of BaO, 0% to 1% of ZrO2, and 0% to 1% of SnO2.
  • 7. The glass disk for a magnetic recording medium according to claim 1, wherein a magnetic layer is provided on a surface of the glass disk.
  • 8. A magnetic recording device, comprising: the glass disk for a magnetic recording medium according to claim 1.
  • 9. A glass substrate for a magnetic recording medium, wherein the glass substrate has a strain point of 695° C. to 740° C., a temperature at 104.5 dPa·s of 1300° C. or lower, and a Young's modulus of 78 GPa or higher.
  • 10. The glass substrate for a magnetic recording medium according to claim 9, wherein the glass substrate contains, as a glass composition, in terms of mol %, 60% to 71% of SiO2, 10% to 16% of Al2O3, 0% to 5% of B2O3, 0% to 0.1% of Na2O, 0% to 1% of K2O, 0% to 12% of MgO, 0% to 12% of CaO, 0% to 10% of SrO, 0% to 10% of BaO, 0% to 1% of ZrO2, and 0% to 1% of SnO2.
Priority Claims (1)
Number Date Country Kind
2020-095964 Jun 2020 JP national
PCT Information
Filing Document Filing Date Country Kind
PCT/JP2021/018708 5/18/2021 WO