Patent Application
20230373839
The present invention relates to a glass manufacturing method.
In recent years, chalcogenide glasses are known as materials suitable for use in the field of infrared optics. Chalcogenide glasses not only have infrared transmissivity but also can be manufactured by press molding. As such, chalcogenide glasses have excellent mass productivity and cost reduction performance.
Patent Document 1 discloses an example of a manufacturing method of a chalcogenide glass. The manufacturing method describes that glass components in a crucible are heated and melted by radiant heat from a heater, and the melt is stirred by a stir bar.
However, in the method described in Patent Document 1, it is necessary to increase the temperature of the heater to a sufficiently high temperature, and further, it is necessary to increase the temperature of the glass components to a target temperature by the radiant heat from the heater. As such, it is difficult to increase the temperature at a sufficiently high speed.
Meanwhile, when decreasing the temperature of the glass components to a target temperature by, for example, switching the heater between ON and OFF, the glass components continue to be heated by the radiant heat from the heater for some time even if the heater is switched to OFF. As such, it is difficult to decrease the temperature at a sufficiently high speed.
An object of the present invention is to provide a glass manufacturing method in which temperature can be increased and decreased easily at a high speed and in which the productivity can be improved.
A glass manufacturing method according to the present invention includes the steps of: making a melt by melting a raw material disposed in a container and obtaining a glass by cooling the melt, wherein the raw material contains a metal; in the step of making the melt from the raw material, the raw material is induction-heated.
The glass manufacturing method according to the present invention preferably further includes the step of stirring the melt, wherein the melt is stirred by a Lorentz force.
The glass manufacturing method according to the present invention preferably further includes the step of discharging the melt to outside of the container through a pipe, wherein the pipe is connected to the container and is provided with a plug in the pipe, and the plug is heated and melted to discharge the melt. In this case, the plug is more preferably a solidified product formed by cooling the melt in the pipe.
The glass is preferably a chalcogenide glass.
The present invention provides a glass manufacturing method in which temperature can be increased and decreased easily at a high speed and in which the productivity can be improved.
A preferred embodiment will be described below. However, the following embodiment is merely an example, and the present invention is not limited to the following embodiment. Moreover, in the drawings, members having substantially the same functions may be referred to by the same reference numerals.
As an example of the present invention, the manufacturing method of the present embodiment is a method of manufacturing a chalcogenide glass. However, the method according to the present invention can also be applied to the manufacturing of glasses that are not chalcogenide glasses.
As illustrated in
A pipe 4 is connected to the bottom portion 2 of the container 1. A pipe sleeve 5 is disposed surrounding the pipe 4. The pipe 4 passes through the inside of the pipe sleeve 5. In the present embodiment, the pipe sleeve 5 is made of Pt. However, the pipe sleeve 5 may be made of any suitable metal.
As illustrated in
Next, as illustrated in
In forming a chalcogenide glass, it is necessary to prevent the heated raw material 6 from reacting with oxygen or moisture. In the present embodiment, since air inside the container 1 is replaced with an inert gas or a reducing gas, oxygen and moisture are removed from the container. Thus, a chalcogenide glass can be suitably formed even without the use of a sealed container kept in a vacuum state. In the present embodiment, as described below, the formed glass can be discharged from the pipe 4 to outside of the container 1; as such, the container 1 can be reused because it is not necessary to destroy the container 1 to remove the formed glass.
Meanwhile, as illustrated in
The application of electric current to the coil 10A generates an induced magnetic field and an induced current, resulting in a Lorentz force being applied to the melt 11. The Lorentz force can stir the melt 11. As such, in the present embodiment, the melt 11 can be stirred without using a means, such as a stirrer, that stirs the melt 11 by bringing a member into direct contact with the melt 11. However, a stirrer or the like may be used to stir the melt 11.
As described above, a portion of the melt 11 is discharged into the pipe 4. The melt 11 in the pipe 4 is cooled and becomes a solidified product (solid glass). In this way, the plug 12 is formed. As such, a small amount of the melt 11 that forms the plug 12 is discharged into the pipe 4, but the discharge of the rest of the melt 11 is stopped by the plug 12. However, a lid, a plunger, or the like may be used instead of the plug 12.
As illustrated in
The discharged melt 11 flows into a suitable mold, for example. The melt 11 is then cooled in the mold, forming a glass.
A feature of the present embodiment is that, the raw material 6 contains a metal, and the raw material 6 is melted by induction-heating. By adjusting the current applied to the coil 10A, the degree of heat build-up in the metal contained in the raw material 6 or the melt can be adjusted, and the temperature of the raw material 6 or the melt 11 can be directly adjusted. As such, it is possible to increase or decrease the temperature more easily and faster than the conventional radiation heating. Therefore, productivity can be increased.
As illustrated in
The pipe 4 may not necessarily be connected to the container 1. However, since the pipe 4 is connected to the container 1, the melt 11 can be easily discharged without the orientation of the container 1 being changed.
The plug 12 in the pipe 4 is preferably formed of a solidified product obtained by cooling the melt 11 in the pipe 4. This makes it possible to stop the discharge of the melt 11 without the use of a member such as a plunger or a lid. As such, a member such as a lid or a plunger does not come into contact with the melt 11, and the melt 11 is less likely to be contaminated. Therefore, the resulting glass can have an increased purity.
Note that when a member such as a plunger or a lid is used, it is necessary to dispose a member having a size that plugs the pipe 4 without any gaps at a correct position. As such, high precision is required for the size and positioning of the member. In comparison, the plug 12 is formed of a solidified product obtained by cooling the melt 11 that has been discharged into the pipe, and thus the plug 12 can plug the pipe 4 more reliably and easily.
The proportion of the materials contained in the raw material 6 of the present embodiment is adjusted to give the resulting glass the following composition. In the description of the composition of the glass, “%” means “mol %”. Note that, for example, the sum of the contents of A, B, and C may be referred to as “content of A+B+C” or “A+B+C”.
A glass formed according to the method of the present embodiment contains greater than 0 mol % and 50 mol % or less of Ge, greater than 0 mol % and 50 mol % or less of Ga, from 30 mol % to 90 mol % of Te, from 0 mol % to 40 mol % of Ag+Al+Ti+Cu+In+Sn+Bi+Cr+Zn+Mn, and from 0 mol % to 50 mol % of F+Cl+Br+I in the glass composition.
Ge is a component for forming a glass network. Ge is also a metalloid. The content of Ge is greater than 0% and 50% or less, preferably from 2% to 40%, more preferably from 4% to 35%, even more preferably from 5% to 30%, further more preferably from 7% to 25%, and still more preferably from 10% to 20%. When the content of Ge is too small, vitrification becomes difficult. Meanwhile, when the content of Ge is too large, Ge-based crystal tends to precipitate, and raw material costs tend to be high.
Ga is a component for increasing thermal stability (stability of vitrification) of glass. Also, Ga is a metal element. The content of Ga is greater than 0% and 50% or less, preferably from 1% to 45%, more preferably from 2% to 40%, even more preferably from 4% to 30%, further more preferably from 5% to 25%, and still more preferably from 10% to 20%. When the content of Ga is too small, vitrification becomes difficult. Meanwhile, when the content of Ga is too large, Ga-based crystal is easy to precipitate, and raw material costs tend to be high.
Te, which is a chalcogen element, is a component essential for forming a glass network. Te is also a metalloid element. The content of Te is from 30% to 90%, preferably from 40% to 89%, more preferably from 50% to 88%, even more preferably from 60% to 86%, and further more preferably from 70% to 85%. When the content of Te is too small, vitrification becomes difficult. Meanwhile, when the content of Te is too large, Te-based crystal is easy to precipitate.
Ag+Al+Ti+Cu+In+Sn+Bi+Cr+Zn+Mn are metal elements. Glass can have an increased thermal stability by containing the above metal elements. The content of Ag+Al+Ti+Cu+In+Sn+Bi+Cr+Zn+Mn is from 0% to 40%, preferably greater than 0% and 30% or less, more preferably greater than 0% and 20% or less, and even more preferably from 0.1% to 10%. When the content of Ag+Al+Ti+Cu+In+Sn+Bi+Cr+Zn+Mn is too small or too large, vitrification becomes difficult. Note that the individual content of each of Ag+Al+Ti+Cu+In+Sn+Bi+Cr+Zn+Mn is from 0% to 40%, preferably from 0% to 30% (with at least one component being greater than 0%), and more preferably from 0% to 20% (with at least one component being greater than 0%), and even more preferably from 0.1% to 10%. Of these, it is preferable to use Ag and/or Sn from the perspective that the effect of increasing thermal stability of glass is particularly great.
In addition to the above components, the glass formed in the present embodiment may contain the following components.
F, Cl, Br, and I are also components that increase thermal stability of glass. A content of F, Cl, Br, and I is from 0% to 50%, preferably from 1% to 40%, more preferably from 1% to 30%, even more preferably from 1% to 25%, and particularly preferably from 1% to 20%. When the content of F+Cl+Br+I is too large, vitrification becomes difficult, and weather resistance tends to be weak. Note that the individual content of each of F, Cl, Br, and I is from 0% to 50%, preferably from 1% to 40%, more preferably from 1% to 30%, even more preferably from 1% to 25%, and particularly preferably from 1% to 20%. Of these, it is preferable to use I because the element raw material can be used and the effect of increasing glass stability is particularly great.
The inclusion of Si, Sb, and Cs results in an increased thermal stability. Here, Si and Sb are metalloids. Si+Sb+Cs is preferably from 0% to 40%, more preferably from 0% to 30%, even more preferably from 0% to 20%, and further more preferably from 0.1% to 10%.
S is a component that widens the vitrification range and tends to improve thermal stability of glass. A content of S is preferably from 0% to 30%, more preferably from 0% to 20%, even more preferably from 0% to 10%, and particularly preferably from 0% to 3%. When the content of S is too large, transmittance of infrared rays having a wavelength of 10 μm or greater tends to be small.
Se and As are components that widen the vitrification range and improve thermal stability of glass. An individual content of each of Se and As is preferably from 0% to 10%, more preferably from 0.5% to 5%. However, since these substances are toxic, the glass is preferably substantially free of Se and As from the viewpoint of reducing the effects on the environment and the human body, as described above.
Note that the glass is preferably substantially free of Cd, Tl, and Pb, which are toxic substances.
A proportion of the metal in the raw material 6 is preferably 80 vol % or greater, more preferably 85 vol % or greater, and particularly preferably 90 vol % or greater. In this way, the raw material 6 can be easily melted by induction-heating. As such, it is possible to increase or decrease the temperature more easily and faster than the conventional radiation heating, and productivity can be increased. An upper limit of the proportion of the metal in the raw material 6 is not limited, but may be, for example, 100 vol % or less, 99 vol % or less, and particularly 98 vol % or less.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-172264 | Oct 2020 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2021/036557 | 10/4/2021 | WO |
