The present disclosure relates to an electrochemical cell device, a module, and a module housing device.
In recent years, various fuel cell stack devices each including a plurality of fuel cells have been proposed, as next-generation energy. The fuel cell is a type of electrochemical cell capable of obtaining electrical power by using a fuel gas such as a hydrogen-containing gas and an oxygen-containing gas such as air. Gases such as a fuel gas and an oxygen-containing gas may be collectively referred to as a reactive gas.
Patent Document 1: WO 2009/131180
In an aspect of an embodiment, an electrochemical cell device includes an electrochemical cell and a support member. The support member supports the electrochemical cell. The support member includes a first portion located on an upstream side in a first direction in which a reactive gas flows, and a second portion located on a downstream side in the first direction with respect to the first portion. The first portion and the second portion have different reflectances to infrared light.
In addition, in an aspect of an embodiment, an electrochemical cell device includes an electrochemical cell and a support member. The support member supports the electrochemical cell. The support member includes a first portion located at a low-temperature portion of the electrochemical cell and a second portion located at a high-temperature portion of the electrochemical cell higher in temperature than the low-temperature portion. The first portion and the second portion have different reflectances to infrared light.
Additionally, a module of the present disclosure includes the electrochemical cell device described above and a storage container storing the electrochemical cell device.
Furthermore, a module housing device of the present disclosure includes the module described above, an auxiliary device configured to operate the module, and an external case that houses the module and the auxiliary device.
In the fuel cell stack device, for example, when the temperature in the electrochemical cell varies, the power generation performance and the durability may be reduced, and there is room for improvement in terms of improving the battery performance.
Therefore, it is expected to provide an electrochemical cell device, a module, and a module housing device having improved battery performance.
Embodiments of an electrochemical cell device, a module, and a module housing device disclosed in the present application will be described below in detail with reference to the accompanying drawings. Note that the disclosure is not limited by the following embodiments.
Note that the drawings are schematic and that the dimensional relationships between elements, the proportions of the elements, and the like may differ from the actual ones. Furthermore, there may be differences between the drawings in the dimensional relationships, proportions, and the like.
First, with reference to
In the example illustrated in
As illustrated in
The element portion 3 is provided on the flat surface n1 of the support substrate 2. The element portion 3 includes a fuel electrode 5, a solid electrolyte layer 6, and an air electrode 8. In the example illustrated in
As illustrated in
Hereinafter, each of constituent members constituting the cell 1 will be described.
The support substrate 2 includes gas-flow passages 2a, in which gas flows. The example of the support substrate 2 illustrated in
The material of the support substrate 2 includes, for example, an iron group metal component and an inorganic oxide. For example, the iron group metal component may be, for example, Ni (nickel) and/or NiO. The inorganic oxide may be, for example, a specific rare earth element oxide. The rare earth element oxide may contain, for example, one or more rare earth elements selected from Sc, Y, La, Nd, Sm, Gd, Dy, and Yb.
As the material of the fuel electrode 5, a commonly known material may be used. As the fuel electrode 5, porous electrically conductive ceramics, for example, ceramics containing: ZrO2 in which a calcium oxide, a magnesium oxide, or a rare earth element oxide is in solid solution, and Ni and/or NiO may be used. This rare earth element oxide may contain a plurality of rare earth elements selected from, for example, Sc, Y, La, Nd, Sm, Gd, Dy, and Yb. Hereinafter, ZrO2 in which a calcium oxide, a magnesium oxide, or a rare earth element oxide is in solid solution may be referred to as stabilized zirconia. Stabilized zirconia also includes partially stabilized zirconia.
The solid electrolyte layer 6 is an electrolyte and delivers ions between the fuel electrode 5 and the air electrode 8. At the same time, the solid electrolyte layer 6 has gas blocking properties, and makes leakage of the fuel gas and the oxygen-containing gas less likely to occur.
A material of the solid electrolyte layer 6 may be, for example, ZrO2 in which 3 mole % to 15 mole % of a rare earth element oxide, calcium oxide, and magnesium oxide are in solid solution. The rare earth element oxide may contain, for example, one or more rare earth elements selected from Sc, Y, La, Nd, Sm, Gd, Dy, and Yb. The solid electrolyte layer 6 may include, for example, CeO2 in which La, Nd, Sm, Gd, or Yb is in solid solution, BaZrO3 in which Sc or Yb is in solid solution, or BaCeO3 in which Sc or Yb is in solid solution.
The air electrode 8 has gas permeability. The open porosity of the air electrode 8 may be, for example, in the range of 20% to 50%, particularly in the range of 30% to 50%.
The material of the air electrode 8 is not particularly limited, as long as the material is one generally used for the air electrode. The material of the air electrode 8 may be, for example, an electrically conductive ceramic such as a so-called ABO3 type perovskite oxide.
The material of the air electrode 8 may be, for example, a composite oxide in which strontium (Sr) and lanthanum (La) coexist at the A site. Examples of such a composite oxide include LaxSr1-xCoyFe1-yO3, LaxSr1-xMnO3, LaxSr1-xFeO3, and LaxSr1-xCoO3. Here, x is 0<x<1, and y is 0<y<1.
When the element portion 3 includes the intermediate layer 7, the intermediate layer 7 functions as a diffusion prevention layer. When an element such as strontium (Sr) contained in the air electrode 8 diffuses into the solid electrolyte layer 6, a resistance layer such as, for example, SrZrO3 is formed in the solid electrolyte layer 6. The intermediate layer 7 suppresses the diffusion of Sr and makes it difficult to form SrZrO3 and other oxides having electrical insulation properties.
A material of the intermediate layer 7 is not particularly limited as long as the material is one generally used for the diffusion suppression layer of an element between the air electrode 8 and the solid electrolyte layer 6. The material of the intermediate layer 7 may contain, for example, cerium oxide (CeO2) in which a rare earth element other than cerium (Ce) is in solid solution. As such a rare earth element, for example, gadolinium (Gd), samarium (Sm), or the like may be used.
The interconnector 4 is dense, and makes the leakage of the fuel gas flowing through the gas-flow passages 2a located inside the support substrate 2, and of the oxygen-containing gas flowing outside the support substrate 2 less likely to occur. The interconnector 4 may have a relative density of 93% or more; particularly 95% or more.
As the material of the interconnector 4, a lanthanum chromite-based perovskite oxide (LaCrO3-based oxide), a lanthanum strontium titanium-based perovskite oxide (LaSrTiO3-based oxide), or the like may be used. These materials have electrical conductivity, and are unlikely to be reduced and also unlikely to be oxidized even when exposed to a fuel gas such as a hydrogen-containing gas and an oxygen-containing gas such as air. In addition, a metal or an alloy may be used as the material of the interconnector 4.
The support substrate 2 may be made of a metal or an alloy as illustrated in
As illustrated in
In the example illustrated in
The gas-flow passage 2a of the support substrate 2 may be made of the member 120 having unevenness as illustrated in
An electrochemical cell device according to the present embodiment using the cell 1 described above will be described with reference to
As illustrated in
The fixing member 12 includes a fixing material 13 and a support member 14. The support member 14 supports the cells 1. The fixing material 13 fixes the cells 1 to the support member 14. The support member 14 includes a support body 15 and a gas tank 16. The support body 15 and the gas tank 16, constituting the support member 14, are made of, for example, a metal and electrically conductive.
The fixing member 12a is positioned so as to face the fixing member 12 with the cell stack 11 interposed therebetween. The fixing member 12 fixes lower end sides of the cells 1, and the fixing member 12a fixes upper end sides of the cells 1. Note that in
As illustrated in
The gas tank 16 includes an opening portion through which a reactive gas is supplied to the plurality of cells 1 via the insertion hole 15a, and a recessed groove 16a located in the periphery of the opening portion. The outer peripheral end portion of the support body 15 is bonded to the gas tank 16 by a bonding material 21, with which the recessed groove 16a of the gas tank 16 is filled.
In the example illustrated in
A hydrogen-rich fuel gas can be produced, for example, by steam-reforming a raw fuel. When the fuel gas is produced by steam reforming, the fuel gas contains steam.
In the example illustrated in
The insertion hole 15a has, for example, an oval shape in a top surface view. The length of the insertion hole 15a in an arrangement direction of the cells 1, that is, the thickness direction T, is longer than the distance between two end current collection members 17 located at two ends of the cell stack 11, for example. The width of the insertion hole 15a is, for example, greater than the length of the cell 1 in the width direction W (see
As illustrated in
The fixing material 13 and the bonding material 21 may be of low electrical conductivity, such as glass. As the specific materials of the fixing material 13 and the bonding material 21, amorphous glass or the like may be used, and especially, crystallized glass or the like may be used.
As the crystallized glass, for example, any one selected from the group consisting of SiO2—CaO-based, MgO—B2O3-based, La2O3—B2O3—MgO-based, La2O3—B2O3—ZnO-based, and SiO2—CaO—ZnO-based materials may be used, or, in particular, a SiO2—MgO-based material may be used.
As illustrated in
As illustrated in
As illustrated in
The positive electrode terminal 19A functions as a positive electrode when the electrical power generated by the cell stack 11 is output to the outside, and is electrically connected to the end current collection member 17 on a positive electrode side in the cell stack 11A. The negative electrode terminal 19B functions as a negative electrode when the electrical power generated by the cell stack 11 is output to the outside, and is electrically connected to the end current collection member 17 on a negative electrode side in the cell stack 11B.
The connection terminal 19C electrically connects the end current collection member 17 on the negative electrode side in the cell stack 11A and the end current collection member 17 on the positive electrode side in the cell stack 11B.
Subsequently, an electrochemical cell device according to a first embodiment will be further described with reference to
As illustrated in
The cell stack device 10 illustrated in
A temperature of the cell 1 rises due to Joule heat associated with power generation. At this time, a temperature distribution of the cell 1 is biased due to the influence of the oxygen-containing gas flowing outside the cell 1, or the like. Specifically, the temperature on a downstream side in the first direction 30, that is, an upper end side of the cell 1 supported by the second member 152 becomes higher than the temperature on an upstream side in the first direction 30, that is, a lower end side of the cell 1 supported by the first member 151. For this reason, in a portion of the cell 1 located on the downstream side in the first direction 30, for example, the temperature becomes higher than a temperature suitable for power generation, and the durability is likely to decrease.
Therefore, in the present embodiment, in an exposed portion of the support body 15 supporting the cell 1, which is exposed to an oxidizing atmosphere, the infrared light reflectance is made different between a first portion located on the upstream side in the first direction 30 and a second portion located on the downstream side in the first direction 30 with respect to the first portion. Specifically, an exposed portion 151a of the first member 151 has a lower infrared light reflectance than an exposed portion 152a of the second member 152.
Thus, on the downstream side of the cell 1 in the first direction 30, an increase in the temperature of the cell 1 due to radiant heat from the second member 152 can be reduced. For this reason, it is possible to make it difficult for a decrease in durability due to overheating of the cell 1 to occur. Therefore, the present embodiment can improve battery performance.
On the other hand, the temperature on the upstream side in the first direction 30 tends to be lower than the temperature on the downstream side in the first direction 30. Therefore, in a portion of the cell 1 located on the upstream side in the first direction 30, for example, the temperature does not reach a temperature suitable for power generation, and the power generation performance is likely to decrease.
In the present embodiment, on the upstream side of the cell 1 in the first direction 30, the temperature rise of the cell 1 can be promoted by the radiant heat from the first member 151. For this reason, it is possible to make it difficult for a decrease in power generation performance due to insufficient heating of the cell 1 to occur. Therefore, the present embodiment can improve battery performance.
Here, materials of the first member 151 and the second member 152 are selected from metal materials or ceramics having different infrared light reflectances. The first member 151 and the second member 152 may be made of, for example, metal materials or ceramics having different surface colors.
The second member 152 may be made of, for example, a metal material such as stainless steel containing chromium. The second member 152 may contain, for example, a metal oxide. In addition, the second member 152 may be made of, for example, aluminum oxide (alumina), magnesium oxide (magnesia), silicon oxide (silica), zirconium oxide (zirconia), chromium oxide (chromia), titanium oxide (titania), a composite oxide thereof, or the like. The zirconia may be stabilized zirconia. The composite oxide may be selected from forsterite, cordierite, and the like, for example. The second member 152 may contain, for example, an impurity such as Al2O3 or CaO. In addition, the second member 152 may have a surface color of, for example, white, yellow, or the like.
The first member 151 may be made of, for example, a metal material such as stainless steel containing chromium. In addition, the first member 151 may be made of, for example, aluminum oxide (alumina), magnesium oxide (magnesia), silicon oxide (silica), zirconium oxide (zirconia), chromium oxide (chromia), titanium oxide (titania), a composite oxide thereof, or the like. The zirconia may be stabilized zirconia. The composite oxide may be selected from forsterite, cordierite, and the like, for example. The composite oxide may contain, for example, an impurity such as Al2O3 or CaO. In addition, the first member 151 may contain, for example, a colored metal oxide containing a transition element such as iron (Fe). The first member 151 may have a surface color of, for example, white, yellow, or black. The first member 151 may be the same type of material or the same type of color as the second member 152 as long as the infrared light reflectance at the exposed portion 151a is lower than that at the exposed portion 152a.
Note that the infrared light reflectance at the exposed portions 151a and 152a can be measured with a near infrared/infrared spectrophotometer or a Fourier transformation infrared spectrometer (FTIR). Infrared light refers to light having a wavelength equal to or longer than 700 nm. When comparing the infrared light reflectance, for example, an average of the reflectances in a range of wavelengths from 1500 nm to 2500 nm may be compared. The infrared light reflectance referred to herein is an average of reflectances in a range of wavelengths from 1500 nm to 2500 nm.
In addition, the first member 151 and/or the second member 152 may be provided with, for example, a coating film having different infrared light reflectances at the exposed portions 151a and 152a.
The coating layer 152b is made of a material that causes the infrared light reflectance at the exposed portion 152a to be higher than that at the exposed portion 151a. The coating layer 152b may be made of, for example, aluminum oxide (alumina), magnesium oxide (magnesia), silicon oxide (silica), zirconium oxide (zirconia), chromium oxide (chromia), titanium oxide (titania), a composite oxide thereof, or the like. The zirconia may be stabilized zirconia. The composite oxide may be selected from forsterite, cordierite, and the like, for example. The coating layer 152b may have a surface color of, for example, white, yellow, or the like. The coating layer 152b may contain, for example, a colored metal oxide containing a transition element such as iron (Fe).
In addition, the coating layer 152b may be electrically conductive. The coating layer 152b may contain, for example, an electrically conductive metal material and/or metal oxide. The electrically conductive metal oxide included in the coating layer 152b may be, for example, a composite oxide having a spinel structure, for example, Zn(CoxMn1-x)2O4 (0<x<1) such as ZnMnCoO4, Mn1.5Co1.5O4, MnCo2O4, CoMn2O4, or the like. The electrically conductive metal oxide may be a so-called ABO3 perovskite oxide. In addition, the electrically conductive metal oxide may be a zinc oxide, for example.
The cell stack device 10 illustrated in
The coating layer 151b is made of a material that causes the infrared light reflectance at the exposed portion 151a to be lower than that at the exposed portion 152a. The coating layer 151b may be made of, for example, aluminum oxide (alumina), magnesium oxide (magnesia), silicon oxide (silica), zirconium oxide (zirconia), chromium oxide (chromia), titanium oxide (titania), a composite oxide thereof, or the like. The zirconia may be stabilized zirconia. The composite oxide may be selected from forsterite, cordierite, and the like, for example. The coating layer 151b may have a surface color of, for example, black. The coating layer 151b may contain, for example, a colored metal oxide containing a transition element such as iron (Fe).
In addition, the coating layer 151b may be electrically conductive. The coating layer 151b may contain, for example, an electrically conductive metal material and/or metal oxide. The electrically conductive metal oxide included in the coating layer 151b may be, for example, a composite oxide having a spinel structure, for example, Zn(CoxMn1-x)2O4 (0<x<1) such as ZnMnCoO4, Mn1.5Co1.5O4, MnCo2O4, CoMn2O4, or the like. The electrically conductive metal oxide may be a so-called ABO3 perovskite oxide. In addition, the electrically conductive metal oxide may be a zinc oxide, for example.
Note that in the cell stack devices 10 illustrated in
The cell stack device 10 illustrated in
When the thickness of the coating layer 151b is smaller than the thickness of the coating layer 152b, the material of the first member 151 may affect the infrared light reflectance at the exposed portion 151a. In this case, for example, even when the materials of the coating layers 151b and 152b are the same, the infrared light reflectance at the exposed portion 151a can be made lower than the infrared light reflectance at the exposed portion 152a.
In the cell stack device 10 illustrated in
Next, a module 100 according to the present embodiment using the electrochemical cell device described above will be described with reference to
As illustrated in
The reformer 102 reforms a raw fuel such as a natural gas or kerosene supplied via a raw fuel supply pipe 103, and produces the fuel gas. Note that the reformer 102 preferably has a structure capable of performing steam reforming, which is an efficient reformation reaction. The reformer 102 can perform the steam reforming by including a vaporizing unit 102a that vaporizes water, and a reforming unit 102b in which a reforming catalyst (not illustrated) is disposed for reforming the raw fuel into the fuel gas.
Then, the fuel gas produced by the reformer 102 is supplied to the fixing member 12 via the gas circulation pipe 20, and the fuel gas is supplied via the fixing member 12 to the gas-flow passages 2a (see
Furthermore, in the module 100 having the configuration described above, during normal power generation, a temperature in the module 100 rises to approximately 500° C. to 1000° C. due to the aforementioned combustion and power generation in the cells 1.
The above-described module 100 is configured such that the cell stack device 10 with improved battery performance is stored therein as described above, whereby the module 100 with improved battery performance can be obtained.
The external case of the module housing device 110 illustrated in
In addition, the dividing plate 113 includes an air circulation hole 116 for causing air in the auxiliary device housing chamber 115 to flow into the module housing chamber 114 side. The external plate 112 constituting the module housing chamber 114 includes an exhaust hole 117 for discharging air inside the module housing chamber 114.
In the module housing device 110 described above, the module 100 with improved battery performance is provided in the module housing chamber 114 as described above, whereby the module housing device 110 with improved battery performance can be obtained.
The cell stack device 10 illustrated in
A temperature of the cell 1 rises due to Joule heat associated with power generation. At this time, a temperature distribution of the cell 1 is biased due to the influence of the oxygen-containing gas flowing outside the cell 1, or the like. Specifically, a temperature of a portion of the cell 1 located on the downstream side in the first direction 30 is more likely to increase than a temperature of a portion located on the upstream side in the first direction 30. For this reason, in the portion of the cell 1 located on the downstream side in the first direction 30, for example, the temperature becomes higher than a temperature suitable for power generation, and the durability is likely to decrease.
In the present embodiment, a coating layer 150b is located on a portion 150 of the support body 15 supporting the cell 1, which is located on the downstream side in the first direction 30 and is located away from the cell 1. Thus, in an exposed portion 150a exposed to an oxidizing atmosphere, the infrared light reflectance is made different between a portion 150d close to the cell 1 and a portion 150c more distant from the cell 1 than the portion 150d is. Specifically, the portion 150c has a lower infrared light reflectance than the portion 150d.
On the downstream side in the first direction 30 of the cell 1 close to the portion 150d, an increase in the temperature of the cell 1 due to radiant heat from the portion 150 of the support body 15 can be reduced. For this reason, it is possible to make it difficult for a decrease in durability due to overheating of the cell 1 to occur. Therefore, the present embodiment can improve battery performance.
In the cell stack device 10 illustrated in
Next, the support body 15 according to variations of the present embodiment will be described with reference to
When the support body 15 having a flat plate shape as illustrated in
In addition, the support body 15 illustrated in
As illustrated in
In each of the embodiments described above, a so-called “vertically striped type” cell stack device, in which only one element portion including a fuel electrode, a solid electrolyte layer, and an air electrode is provided on the surface of the support substrate, has been exemplified. However, the embodiments can be applied to a horizontally striped type cell stack device with a stack of so-called “horizontally striped type” cells, in which a plurality of element portions are provided on the surface of a support substrate at mutually separated locations and adjacent element portions are electrically connected to each other.
In addition, in the embodiments described above, the case where the hollow flat plate-type support substrate is used has been exemplified; however, the embodiments can also be applied to a cell stack device using a cylindrical support substrate. As will be described later, the embodiments can also be applied to a flat plate cell stack device in which so-called “flat plate” cells are stacked in the thickness direction.
The cell 1 is of a flat plate type and includes a first portion 1a and a second portion 1b. In the first portion 1a, the fuel gas flows from the manifold 155 toward the communicating member 156. In the second portion 1b, the fuel gas flows from the communicating member 156 toward the manifold 155. The manifold 155 may include a supply portion 1551 that supplies the fuel gas to the first portion 1a and a collection portion 1552 that collects the gas flowing from the second portion 1b. The manifold 155 may include a partition wall 1553 that separates the supply portion 1551 and the collection portion 1552 so that the fuel gas in the supply portion 1551 supplied to the first portion 1a and the fuel gas in the collection portion 1552 collected from the second portion 1b are not mixed with each other.
As illustrated in
In this case, the infrared light reflectance at the exposed portion 155a may be lower than the infrared light reflectance at the exposed portion 155b, and the infrared light reflectance at the exposed portion 156a may be lower than the infrared light reflectance at the exposed portion 156b. This reduces variation in the temperature in the cell 1 and can improve battery performance. In the third embodiment, a hollow flat plate-type cell 1 may be used instead of the flat plate-type cell 1. The communicating member 156 may support one end of the plurality of cells 1, but each cell 1 may individually have the communicating member 156, and the communicating members may be separated from each other.
In each of the embodiments described above, a fuel cell, a fuel cell stack device, a fuel cell module, and a fuel cell device have been illustrated as examples of the “electrochemical cell”, the “electrochemical cell device”, the “module”, and the “module housing device”; however, they may be an electrolytic cell, an electrolytic cell stack device, an electrolytic module, and an electrolytic device, respectively, as other examples. The electrolytic cell includes a hydrogen electrode and an oxygen electrode, and decomposes water vapor into hydrogen and oxygen by supplying electrical power. In addition, although the oxide ion conductor or the hydrogen ion conductor has been described as an example of the electrolyte material of the electrochemical cell in the above embodiments, the electrolyte material may be a hydroxide ion conductor.
In addition, in the first and second embodiments, the first portion and the second portion with different infrared light reflectances are located on the surface of the support body 15. However, no such limitation is intended, and the first portion and the second portion may be located on the surface of the gas tank 16, for example. Additionally, the first portion and the second portion may be parts of the exposed portion exposed to the oxygen-containing gas. Furthermore, the first portion and the second portion may be located on a surface of a current collector, an interconnector, an end plate, or the like of a so-called flat plate cell. The first portion and the second portion may be located on surfaces of the support substrate 2, the member 120, and the like of the cell 1 illustrated in
Additionally, in each of the embodiments described above, the downstream side of the cell 1 in the first direction 30 is likely to be higher in temperature than the upstream side thereof and the upstream side of the cell 1 in the first direction 30 is likely to be lower in temperature than the downstream side thereof. In other words, the high-temperature portion is located on the downstream side of the cell 1 in the first direction 30 and the low-temperature portion is located on the upstream side thereof in the first direction 30. However, since the temperature distribution in the cell stack device 10 may vary depending on, for example, the structures of the cell stack 11 and the gas-flow passage, and the like, the arrangement of the high-temperature portion and the low-temperature portion is not limited to one described above. For example, the high-temperature portion may be located at a center of the cell stack 11, and the low-temperature portion may be located at an end portion of the cell stack 11. In addition, in the electrochemical cell device according to the second embodiment, for example, the high-temperature portion may be located at a central portion of the element portion included in the flat plate-type cell or the cell 1 illustrated in
While the present disclosure has been described in detail, the present disclosure is not limited to the aforementioned embodiment, and various changes, improvements, and the like can be made without departing from the gist of the present disclosure.
As described above, an electrochemical cell device (for example, the cell stack device 10) according to the embodiment includes an electrochemical cell (for example, the cell 1) and the support member 14 (support body 15). The support member 14 supports the electrochemical cell. The support member 14 includes a first portion located on an upstream side in the first direction 30 in which a reactive gas flows and a second portion located on a downstream side in the first direction 30 with respect to the first portion. The first portion and the second portion have different infrared light reflectances. This can improve battery performance of the electrochemical cell device.
The module 100 according to the embodiment includes the electrochemical cell device (for example, the cell stack device 10) described above, and the storage container 101 housing the electrochemical cell device. As a result, the module 100 with improved battery performance may be obtained.
The module housing device 110 according to the embodiment includes the module 100 described above, the auxiliary device configured to operate the module 100, and the external case housing the module 100 and the auxiliary device. Thus, the module housing device 110 with improved battery performance can be obtained.
Note that the embodiments disclosed herein are exemplary in all respects and not restrictive. The aforementioned embodiments can be embodied in a variety of forms. The aforementioned embodiments may be omitted, replaced, or changed in various forms without departing from the scope of the appended claims and the purpose thereof.
Number | Date | Country | Kind |
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2021-141976 | Aug 2021 | JP | national |
Filing Document | Filing Date | Country | Kind |
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PCT/JP2022/032889 | 8/31/2022 | WO |