Patent Grant
11298745
The present application is a national phase entry under 35 U.S.C. § 371 of International Application No. PCT/KR2017/003613 filed on Apr. 3, 2017, which claims priority from Korean Patent Application No. 10-2016-0040361 filed on Apr. 1, 2016, and Korean Patent Application No. 10-2017-0040971 filed on Mar. 30, 2017, the disclosures of which are incorporated herein by reference in their entireties.
This application claims the benefit of priority based on Korean Patent Application No. 10-2016-0040361 filed on Apr. 1, 2016, and Korean Patent Application No. 10-2017-0040971 filed on Mar. 30, 2017, the disclosures of which are incorporated herein by reference in their entireties.
The present application relates to a method for manufacturing a metal foam.
Metal foams can be applied to various fields including lightweight structures, transportation machines, building materials or energy absorbing devices, and the like by having various and useful properties such as lightweight properties, energy absorbing properties, heat insulating properties, refractoriness or environment-friendliness. The metal foams not only have a high specific surface area, but also can further improve the flow of fluids, such as liquids and gases, or electrons, and thus can also be usefully used by being applied in a substrate for a heat exchanger, a catalyst, a sensor, an actuator, a secondary battery, a gas diffusion layer (GDL) or a microfluidic flow controller, and the like.
It is an object of the present invention to provide a method capable of manufacturing a metal foam comprising pores uniformly formed and having excellent mechanical strength as well as a desired porosity.
In this specification, the term metal foam or metal skeleton means a porous structure comprising a metal as a main component. Here, the metal as a main component means that the proportion of the metal is 55% by weight or more, 60% by weight or more, 65% by weight or more, 70% by weight or more, 75% by weight or more, 80% by weight or more, 85% by weight or more, 90% by weight or more, or 95% by weight or more based on the total weight of the metal foam or the metal skeleton. The upper limit of the proportion of the metal contained as the main component is not particularly limited and may be, for example, about 100% by weight, 99% by weight or 98% by weight or so.
The term porous property herein may mean a case where porosity is at least 30% or more, 40% or more, 50% or more, 60% or more, 70% or more, 75% or more, or 80% or more. The upper limit of the porosity is not particularly limited, and may be, for example, less than about 100%, about 99% or less, or about 98% or less or so. The porosity can be calculated in a known manner by calculating the density of the metal foam or the like.
The method for manufacturing a metal foam of the present application may comprise a step of sintering a green structure containing a metal component. In the present application, the term green structure means a structure before the process performed to form the metal foam, such as the sintering process, that is, a structure before the metal foam is formed. In addition, even when the green structure is referred to as a porous green structure, the structure is not necessarily porous per se, and may be referred to as a porous green structure for convenience, if it can finally form a metal foam, which is a porous metal structure.
In the present application, the green structure may comprise a metal component and a salt, and a mixture comprising the metal component and the salt may be molded to form the green structure.
In one example, the metal component may comprise at least a metal having a predetermined relative magnetic permeability and conductivity. According to one example of the present application, when an induction heating method as described below is applied as the sintering, the sintering according to the relevant method can be smoothly carried out by the application of such a metal.
For example, as the metal, a metal having a relative magnetic permeability of 90 or more may be used. The relative magnetic permeability (μr) is the ratio (μ/μ0) of the magnetic permeability (μ) of the relevant material to the magnetic permeability (μ0) in the vacuum. The metal may have a relative magnetic permeability of 95 or more, 100 or more, 110 or more, 120 or more, 130 or more, 140 or more, 150 or more, 160 or more, 170 or more, 180 or more, 190 or more, 200 or more, 210 or more, 220 or more, 230 or more, 240 or more, 250 or more, 260 or more, 270 or more, 280 or more, 290 or more, 300 or more, 310 or more, 320 or more, 330 or more, 340 or more, 350 or more, 360 or more, 370 or more, 380 or more, 390 or more, 400 or more, 410 or more, 420 or more, 430 or more, 440 or more, 450 or more, 460 or more, 470 or more, 480 or more, 490 or more, 500 or more, 510 or more, 520 or more, 530 or more, 540 or more, 550 or more, 560 or more, 570 or more, 580 or more, or 590 or more. The higher the relative magnetic permeability is, the higher the heat is generated at the time of application of the electromagnetic field for induction heating as described below, and thus the upper limit thereof is not particularly limited. In one example, the upper limit of the relative magnetic permeability may be, for example, about 300,000 or less.
The metal may be a conductive metal. The term conductive metal may mean a metal having a conductivity at 20° C. of about 8 MS/m or more, 9 MS/m or more, 10 MS/m or more, 11 MS/m or more, 12 MS/m or more, 13 MS/m or more, or 14.5 MS/m, or an alloy thereof. The upper limit of the conductivity is not particularly limited, and for example, the conductivity may be about 30 MS/m or less, 25 MS/m or less, or 20 MS/m or less.
In the present application, the metal having the relative magnetic permeability and conductivity as above may also be simply referred to as a conductive magnetic metal.
By applying the conductive magnetic metal, sintering can be more effectively performed when the induction heating process to be described below is carried out. Such a metal can be exemplified by nickel, iron or cobalt, but is not limited thereto.
If necessary, the metal component may comprise, together with the conductive magnetic metal, a second metal different from the metal. In this case, the metal foam may be formed of a metal alloy. As the second metal, a metal having the relative magnetic permeability and/or conductivity in the same range as the above-mentioned conductive magnetic metal may also be used, and a metal having the relative magnetic permeability and/or conductivity outside the range may be used. In addition, the second metal may also comprise one or two or more metals. The kind of the second metal is not particularly limited as long as it is different from the conductive magnetic metal to be applied, and for example, one or more metals, different from the conductive magnetic metal, of copper, phosphorus, molybdenum, zinc, manganese, chromium, indium, tin, silver, platinum, gold, aluminum or magnesium, and the like may be applied, without being limited thereto.
The proportion of the conductive magnetic metal in the metal component or the green structure is not particularly limited. For example, the proportion can be adjusted so as to generate an appropriate Joule heat when applying the induction heating method as described below. For example, the metal component or green structure may comprise the conductive magnetic metal in an amount of 30% by weight or more based on the weight of the entire metal component. In another example, the proportion of the conductive magnetic metal in the metal component or green structure may be about 35% by weight or more, about 40% by weight or more, about 45% by weight or more, about 50% by weight or more, about 55% by weight or more, 60% by weight or more, 65% by weight or more, 70% by weight or more, 75% by weight or more, 80% by weight or more, 85% by weight or more, or 90% by weight or more. The upper limit of the conductive magnetic metal proportion is not particularly limited, and for example, the proportion of the conductive magnetic metal in the metal component or green structure may be less than about 100% by weight, or 95% by weight or less. However, the above proportion is an exemplary ratio. For example, since the heat generated by induction heating due to application of an electromagnetic field can be adjusted according to the strength of the electromagnetic field applied, the electrical conductivity and resistance of the metal, and the like, the ratio can be changed depending on specific conditions.
The metal component forming the green structure may be in the form of powder. For example, the metals in the metal component may have an average particle diameter in a range of about 0.1 μm to about 200 μm. In another example, the average particle diameter may be about 0.5 μm or more, about 1 μm or more, about 2 μm or more, about 3 μm or more, about 4 μm or more, about 5 μm or more, about 6 μm or more, about 7 μm or more, or about 8 μm or more. In another example, the average particle diameter may be about 150 μm or less, 100 μm or less, 90 μm or less, 80 μm or less, 70 μm or less, 60 μm or less, 50 μm or less, 40 μm or less, 30 μm or less, or 20 μm or less. As the metal in the metal component, those having different average particle diameters may also be applied. The average particle diameter can be selected from an appropriate range in consideration of the shape of the desired metal foam, for example, the thickness or porosity of the metal foam, and the like.
The green structure may comprise a salt together with the metal component. The salt contained in the green structure serves to form pores of the metal foam. Since the salt is stable even at high temperature, the salt may remain undecomposed while the metal component is being fused in the sintering process, and if such a salt is removed in the subsequent process, pores may be formed at positions where the salt exist.
The kind of salt which can be applied in the present application is not particularly limited, and for example, those which can be well dissolved in a solvent used for removing salts, such as water, can be used. The usable salt is NaCl, KCl, K2CO3, KOH, NaOH, CsCl, CaCl2, MgBr2, MgCl2, Na2SiO3, Na2CO3, NaHCO3, NH4Br or NH4Cl, and the like, but is not limited thereto.
The size, shape and ratio of the salt are not particularly limited and can be selected depending on the structure of the desired metal foam. That is, the shape and size of the pores in the metal foam can be determined by the size or shape of the salt applied in the present application, and the ratio thereof can affect the overall porosity, and thus in consideration of this, the salt having an appropriate size and shape can be applied in a proper ratio.
For example, the salt may have an average particle diameter of about 30 μm or more, or about 40 μm or more. The average particle diameter of the salt may be, for example, about 250 μm or less, about 200 μm or less, about 190 μm or less, 180 μm or less, 170 μm or less, 160 μm or less, 150 μm or less, 140 μm or less, 130 μm or less, 120 μm or less, 110 μm or less, or 100 μm or less or so.
The form of the salt may be variously selected from, for example, spherical, ellipsoidal, polygonal and amorphous shapes, and the like.
In the green structure, the salt may be contained, for example, in a ratio of about 10 to 1,000 parts by weight, relative to 100 parts by weight of the metal component. In another example, such a ratio may be about 15 parts by weight or more, about 20 parts by weight or more, about 30 parts by weight or more, about 40 parts by weight or more, about 50 parts by weight or more, about 60 parts by weight or more, about 70 parts by weight or more, about 80 parts by weight or more, about 90 parts by weight or more, about 95 parts by weight or more, and may be about 900 parts by weight or less, about 800 parts by weight or less, about 700 parts by weight or less, about 600 parts by weight or less, about 500 parts by weight or less, about 400 parts by weight or less, about 300 parts by weight or less, about 200 parts by weight or less, about 190 parts by weight or less, about 180 parts by weight or less, about 170 parts by weight or less, about 160 parts by weight or less, about 150 parts by weight or less, about 140 parts by weight or less, about 130 parts by weight or less, about 120 parts by weight or less, or about 110 parts by weight or less.
The green structure may also comprise known additives, which are additionally required, in addition to the above-mentioned components. An example of such an additive can be exemplified by solvents or binders, and the like, but is not limited thereto.
The manner of forming the green structure is not particularly limited. In the field of manufacturing metal foams, various methods for forming green structures are known, and in the present application all of these methods can be applied. For example, the green structure may be formed by holding a mixture of the metal component and the salt in a proper template, or by coating the mixture in an appropriate manner.
The shape of such a green structure is not particularly limited as it is determined depending on the desired metal foam. In one example, the green structure may be in the form of a film or a sheet. For example, when the structure is in the form of a film or a sheet, the thickness may be 5,000 μm or less, 3,500 μm or less, 2,000 μm or less, 1000 μm or less, 800 μm or less, 700 μm or less, or 500 μm or less. Metal foams have generally brittle characteristics due to their porous structural features, so that there are problems that they are difficult to be manufactured in the form of films or sheets, particularly thin films or sheets, and are easily broken even when they are made. However, according to the method of the present application, it is possible to form a metal foam having pores uniformly formed inside and excellent mechanical properties as well as a thin thickness.
Here, the lower limit of the structure thickness is not particularly limited. For example, the film or sheet shaped structure may have a thickness of about 10 μm or more, 50 μm or more, or about 100 μm or more.
The metal foam can be manufactured by sintering the green structure formed in the above manner. In this case, a method of performing the sintering for producing the metal foam is not particularly limited, and a known sintering method can be applied. That is, the sintering can proceed by a method of applying an appropriate amount of heat to the green structure in an appropriate manner.
As a method different from the existing known method, in the present application, the sintering can be performed by an induction heating method. That is, as described above, the metal component comprises the conductive magnetic metal having the predetermined magnetic permeability and conductivity, and thus the induction heating method can be applied. By such a method, it is possible to smoothly manufacture metal foams having excellent mechanical properties and whose porosity is controlled to the desired level as well as comprising uniformly formed pores.
Here, the induction heating is a phenomenon in which heat is generated from a specific metal when an electromagnetic field is applied. For example, if an electromagnetic field is applied to a metal having a proper conductivity and magnetic permeability, eddy currents are generated in the metal, and Joule heating occurs due to the resistance of the metal. In the present application, a sintering process through such a phenomenon can be performed. In the present application, the sintering of the metal foam can be performed in a short time by applying such a method, thereby ensuring the processability, and at the same time, the metal foam having excellent mechanical strength as well as being in the form of a thin film having a high porosity can be produced.
The sintering process may comprise a step of applying an electromagnetic field to the green structure. By the application of the electromagnetic field, Joule heat is generated by the induction heating phenomenon in the conductive magnetic metal of the metal component, whereby the structure can be sintered. At this time, the conditions for applying the electromagnetic field are not particularly limited as they are determined depending on the kind and ratio of the conductive magnetic metal in the green structure, and the like.
For example, the induction heating can be performed using an induction heater formed in the form of a coil or the like.
The induction heating can be performed, for example, by applying a current of 100 A to 1,000 A or so. In another example, the applied current may have a magnitude of 900 A or less, 800 A or less, 700 A or less, 600 A or less, 500 A or less, or 400 A or less. In another example, the current may have a magnitude of about 150 A or more, about 200 A or more, or about 250 A or more.
The induction heating can be performed, for example, at a frequency of about 100 kHz to 1,000 kHz. In another example, the frequency may be 900 kHz or less, 800 kHz or less, 700 kHz or less, 600 kHz or less, 500 kHz or less, or 450 kHz or less. In another example, the frequency may be about 150 kHz or more, about 200 kHz or more, or about 250 kHz or more.
The application of the electromagnetic field for the induction heating can be performed within a range of, for example, about 1 minute to 10 hours. In another example, the application time may be about 9 hours or less, about 8 hours or less, about 7 hours or less, about 6 hours or less, about 5 hours or less, about 4 hours or less, about 3 hours or less, about 2 hours or less, about 1 hour or less, or about 30 minutes or less.
The above-mentioned induction heating conditions, for example, the applied current, the frequency and the application time, and the like may be changed in consideration of the kind and the ratio of the conductive magnetic metal, as described above.
The sintering of the green structure may be carried out only by the above-mentioned induction heating, or may also be carried out by applying an appropriate heat, together with the induction heating, that is, the application of the electromagnetic field, if necessary.
Following the sintering process, the manufacturing method of the present application may further perform a process of removing the salt from the sintered green structure. By removing the salt after sintering, the metal foam can be formed, while voids are formed in the portions where the salt is present.
The method of removing the salt is not particularly limited, and the salt can be removed by treating the sintered green structure with a solvent capable of dissolving the salt, such as water.
The present application is also directed to a metal foam. The metal foam may be one manufactured by the above-mentioned method. Such a metal foam may comprise, for example, at least the above-described conductive magnetic metal. The metal foam may comprise, on the basis of weight, 30% by weight or more, 35% by weight or more, 40% by weight or more, 45% by weight or more, or 50% by weight or more of the conductive magnetic metal. In another example, the proportion of the conductive magnetic metal in the metal foam may be about 55% by weight or more, 60% by weight or more, 65% by weight or more, 70% by weight or more, 75% by weight or more, 80% by weight or more, 85% by weight or more, or 90% by weight or more. The upper limit of the proportion of the conductive magnetic metal is not particularly limited, and may be, for example, less than about 100% by weight or 95% by weight or less.
The metal foam may have a porosity in a range of about 40% to 99%. As mentioned above, according to the method of the present application, porosity and mechanical strength can be controlled, while comprising uniformly formed pores. The porosity may be 50% or more, 60% or more, 70% or more, 75% or more, or 80% or more, or may be 95% or less, or 90% or less.
The metal foam may also be present in the form of thin films or sheets. In one example, the metal foam may be in the form of films or sheets. The metal foam of such a film or sheet form may have a thickness of 2,000 μm or less, 1,500 μm or less, 1,000 μm or less, 900 μm or less, 800 μm or less, 700 μm or less, 600 μm or less, 500 μm or less, 400 μm or less, 300 μm or less, 200 μm or less, 150 μm or less, about 100 μm or less, about 90 μm or less, about 80 μm or less, about 70 μm or less, about 60 μm or less, or about 55 μm or less. The film or sheet shaped metal foam may have a thickness of about 10 μm or more, about 20 μm or more, about 30 μm or more, about 40 μm or more, about 50 μm or more, about 100 μm or more, about 150 μm or more, about 200 μm or more, about 250 μm or more, about 300 μm or more, about 350 μm or more, about 400 μm or more, about 450 μm or more, or about 500 μm or more, but is not limited thereto.
The metal foam can be utilized in various applications where a porous metal structure is required. In particular, according to the method of the present application, it is possible to manufacture a thin film or sheet shaped metal foam having excellent mechanical strength as well as the desired level of porosity, as described above, thus expanding applications of the metal foam as compared to the conventional metal foam.
The present application can provide a method for manufacturing a metal foam, which is capable of forming a metal foam comprising uniformly formed pores and having excellent mechanical properties as well as the desired porosity, and a metal foam having the above characteristics. In addition, the present application can provide a method capable of forming a metal foam in which the above-mentioned physical properties are ensured, while being in the form of a thin film or sheet, and such a metal foam.
Hereinafter, the present application will be described in detail by way of examples and comparative examples, but the scope of the present application is not limited to the following examples.
A powder of nickel metal, which is the conductive magnetic metal, was used as a metal component. The nickel metal powder sieved through a 200-mesh sieve was mixed with NaCl as a salt in a weight ratio of 1:1. Here, as the NaCl, those having a particle diameter distribution within a range of about 50 μm to 100 μm were used. On the other hand, in the above nickel, the conductivity at 20° C. is about 14.5 MS/m and the relative magnetic permeability is about 600 or so.
The prepared mixture was coated on a quartz plate in the form of a sheet having a thickness of about 600 μm to produce a green structure, and an electromagnetic field was applied to the green structure with a coil-type induction heater. The electromagnetic field was formed by applying a current of about 350 A at a frequency of about 380 kHz, and the electromagnetic field was applied for about 3 minutes. After application of the electromagnetic field, the sintered green structure was immersed in water and washed with sonication to remove the salt, thereby manufacturing a sheet form of metal foam having a thickness in a level of about 600 μm. The manufactured sheet had a porosity of about 53%.
A metal foam was manufactured in the same manner as in Example 1, except that the weight ratio of the nickel metal powder and NaCl was changed to 1:1.5 (nickel metal powder: NaCl). The manufactured sheet had a porosity of about 70% or so.
A metal foam sheet was manufactured in the same manner as in Example 1, except that Na2SiO3 having a particle diameter distribution in a range of about 50 μm to 70 μm was applied as a salt. The manufactured sheet had a porosity of about 55%.
A metal foam sheet was manufactured in the same manner as in Example 1, except that Na2CO3 having a particle diameter distribution in a range of about 150 μm to 200 μm was applied as a salt. The manufactured sheet had a porosity of about 43%.
A metal foam sheet was manufactured in the same manner as in Example 1, except that KCl having a particle diameter distribution in a range of about 70 μm to 100 μm was applied as a salt. The manufactured sheet had a porosity of about 62%.
A metal foam sheet was manufactured in the same manner as in Example 1, except that NH4Cl having a particle diameter distribution in a range of about 25 μm to 55 μm was applied as a salt. The manufactured sheet had a porosity of about 58%.
A metal foam sheet was manufactured in the same manner as in Example 1, except that CaCl2 having a particle diameter distribution in a range of about 70 μm to 110 μm was applied as a salt. The manufactured sheet had a porosity of about 60%.
A metal foam sheet was manufactured in the same manner as in Example 1, except that MgCl2 having a particle diameter distribution in a range of about 50 μm to 70 μm was applied as a salt. The manufactured sheet had a porosity of about 42%.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2016-0040361 | Apr 2016 | KR | national |
| 10-2017-0040971 | Mar 2017 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2017/003613 | 4/3/2017 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2017/171510 | 10/5/2017 | WO | A |
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