Patent Application
20130216743
The disclosure relates to a method for generating a closed-pore metal foam, in which a composite comprising a metal or a metal alloy and a blowing agent is provided. This composite is subjected to a heat treatment, the heating of the composite being sufficient for the blowing agent to form a blowing gas with closed pores being formed in the composite. This means that the closed pores are generated by the blowing gas being generated and trapped in the closed pores as they are formed.
The disclosure furthermore relates to a component which consists at least partially of a closed-pore metal foam.
A component having a closed-pore metal foam part and a method for its production is known, for example, from U.S. Pat. No. 5,151,246. The component may for example consist of a sleeve, in the interior of which the closed-pore metal foam is accommodated. Blowing agents, for example metal hydrides, in particular titanium hydride, or carbonates, for example calcium carbonate, are used in order to produce this closed-pore metal foam part. From these blowing agents and the metal which is intended to form the metal foam, a composite is produced, which may for example consist of particles of the two substances and which is compacted by pressing. The green body formed in this way can subsequently be subjected to a heat treatment, in which case the temperature must be high enough so that, on the one hand, bonding takes place between the individual powder particles of the metal and, on the other hand, the blowing agent forms a blowing gas. In order to ensure bonding between the metal particles, at least diffusion processes between the particles must be made possible. To this end, sufficient heating of the metal substance must be carried out. With said blowing agents, particles of metals which have a solidus temperature of up to 660° can be foamed.
Metal foams are used, for example, in order to seal housing structures. According to WO 2008/145173 A1, this is for example advantageous in the case of gas discharge lamps which are mounted in a lamp body. In order to permit electrical contacting, contacts must be fed out from the lamp body, in which case hermetic sealing of these feed-throughs must be ensured so that no oxygen enters the interior of the lamp. The feed-through between the lamp body and the metal electrode can be reliably filled by means of a metal foam.
Furthermore, the chosen blowing agent must be selected in terms of its thermal properties in such a way that it is compatible with the solidus temperature of the metal to be foamed (or of the metal alloy to be foamed). In this case, the temperature difference between the solidus temperature of the metal and the lower temperature, at which the blowing agent releases the blowing gas, must not be more than 120° C. Only in this way is it possible to ensure that a metal foam is formed reliably. When metal foams are referred to below, this is also meant to include foams of metal alloys.
In one embodiment, a method for generating a closed-pore metal foam is provided, wherein a composite comprising a metal or a metal alloy and a blowing agent is provided, the composite is subjected to a heat treatment, the heating of the composite being sufficient for the blowing agent to form a blowing gas with closed pores being formed in the composite, and molecules of C and/or molecules of B and N, which have a spherical or tubular structure, are used as the blowing agent, the blowing gas being chemically or physically bound to these molecules.
In a further embodiment, the blowing agent is bound to the molecules by a functionalization of the latter or coating the latter. In a further embodiment, the functionalization of the molecules is carried out by bonding the functional group —COOMe, where Me is in particular Mo, Ni, Ir or Co. In a further embodiment, spherical molecules, in which the blowing gas is enclosed, are used as molecules. In a further embodiment, helium and/or nitrogen is enclosed in the molecules as blowing gas. In a further embodiment, the composite is formed from metal particles or metal alloy particles, at least some of these particles being coated with a coat of the blowing agent. In a further embodiment, the composite consists of a coat comprising a plurality of layers, successive layers of the metal or the metal alloy and of the blowing agent being provided. In a further embodiment, a material having a negative thermal expansion coefficient is additionally introduced into the composite.
In another embodiment, a component which consists at least partially of a closed-pore metal foam is provided, wherein molecules of C and/or molecules of B and N, which have a spherical or tubular structure, are contained in the metal foam.
In a further embodiment, the component is formed as a housing structure comprising a material which is different to the metal foam and comprises a cavity having an opening, which is closed by the metal foam. In a further embodiment, the cavity is formed by a glass body, in particular a lamp. In a further embodiment, a material having a negative thermal expansion coefficient is additionally provided in the metal foam, the proportion of which is selected in such a way that the metal foam has at least essentially the same expansion coefficient as the housing structure in the region of the opening.
Example embodiments will be explained in more detail below with reference to figures, in which:
Some embodiments provide a method for generating a closed-pore metal foam and a component comprising such a closed-pore metal foam, in which metals having a solidus temperature of more than 660° C. can be used.
In some embodiments, molecules of C and/or molecules of B and N, which have a spherical or tubular structure, are used as the blowing agent, the blowing gas being chemically or physically bound to these molecules. The spherical molecules are known, for example, as so-called fullerenes. These are regular structures, for example of C atoms. A particular example is the fullerene denoted as C60, the structure of which resembles a soccer ball. As tubular structures, carbon nanotubes (abbreviated to CNT below) or boron nitride nanotubes (referred to below as BNNT) are known. Chemical binding of the blowing agent may, for example, be carried out by functionalization of these molecules. A functional group which is suitable as a blowing agent is, for example, —COOMe. This group may for example be bound to a C atom of a CNT, Me standing in particular for Mo, Ni, Ir or Co. The blowing agent obtained in this way reacts in the presence of a reaction partner such as O2 in a temperature range in excess of 1000° C. CO2 is typically released in this case, which then acts as a blowing gas. With this example of a blowing agent, metals which have a solidus temperature of more than 1000° can thus be processed to form foams.
It is also possible for the blowing agent to be bound to the molecules by coating the latter. In this case, very thin coats having a thickness of one or more atomic layers are applied for example by an ALD method (ALD stands for atomic layer deposition). In this case, the nanoparticles are kept in motion by a turbulent flow method. This method is already known. The particles to be coated may, for example, be CNTs or BNNTs. Typically, these molecules may be coated with titanium hydride or noble-metal oxides, for example iridium oxide and/or molybdenum oxide and/or platinum oxide and/or copper(I) oxide and/or magnetide and/or vanadium pentoxide. The use of noble-metal oxides is advantageous since, owing to their low affinity for oxygen, they decompose more readily into the metal component and an oxygen component, which provides the blowing agent. This is done at temperatures which are of interest for the formation of metal foams. For example, iridium oxide and platinum oxide decompose at temperatures of around 1200° C., ruthenium oxide and rhodium oxide at temperatures of approximately 1100° C. and molybdenum oxide likewise at 1100° C. Oxides having even higher decomposition temperatures are magnetide with a decomposition temperature of 1580° C., copper(I) oxide with a decomposition temperature of 1800° C. and vanadium pentoxide with a decomposition temperature of 1750° C. The oxides can therefore be selected suitably according to the solidus temperature of the metal used for the foaming, in which case it is necessary to take into account the fact that the decomposition temperature of the selected metal oxide must be lower than the relevant solidus temperature of the metal used, specifically by up to 120° C.
If spherical molecules are used as the molecules, then according to some embodiments the blowing gas may also be enclosed in these molecules, i.e. may already exist as a blowing gas at room temperature. However, it will not be released until the spherical molecules are broken down. To this end, they need to be heated to 1500° C. Gas-filled fullerenes may for example contain He or N2, these being referred to as He@C60 or N2@C60. When the gas is released from the interior of the fullerenes, after decomposition of the latter it is available as a blowing gas. This means that even metals having a solidus temperature of about 1600° C. can be foamed with such blowing agents.
According to another embodiment, the composite is formed from metal particles or metal alloy particles, at least some of these particles being coated with a coat of the blowing agent. In this case, even before the metal particles are processed to form a component (green compact), the blowing agent is thus already packaged in such a way that the blowing agent is already incorporated into the green compact during production of the green compact. The concentration of the blowing agent can be adjusted by the thickness of the coating on the particles, the particle size and/or the proportion of coated particles in relation to uncoated particles. This advantageously provides a very accurate method for adjusting the blowing agent concentration. The concentration of the blowing agent subsequently dictates the size and the concentration of pores in the metal foam, and therefore also its density.
Another embodiment is obtained when the composite consists of a coat comprising a plurality of layers, successive layers of the metal or the metal alloy and of the blowing agent being provided. It is particularly advantageous for layers of the blowing agent and layers of the metal alloy, or of the metal, to alternate with one another. The concentration of blowing agent can be adjusted by the thickness ratio of the metal coats to the blowing agent coats. The layers must, however, be made thin enough that uniform distribution of the blowing gas in the composite can take place, so that uniform distribution of the pores in the foam being formed also takes place. In this way, components having particularly large surfaces can advantageously be coated very economically with coats of a metal foam.
It is particularly advantageous for a material having a negative thermal expansion coefficient additionally to be introduced into the composite. This may for example, as already explained above for the blowing agent, be carried out by coating particles or providing layers of this material between other layers of the metal, or of the blowing agent. If materials having a negative thermal expansion coefficient are provided in the metal foam, it is thereby possible to influence the thermal expansion coefficient of the metal foam, which is reduced by means of this. A prerequisite, however, is that the material is thermally stable enough for it to withstand the heat treatment necessary for the formation of the metal foam.
The thermal expansion coefficient of the metal foam reduced by the material is advantageous in particular when the metal foam is brought in contact with components that have a lower thermal expansion coefficient than the metal foam without the part comprising the material having the negative thermal expansion coefficient. For example, metal foams can advantageously be bonded reliably to ceramic components or vitreous components by this measure. The bond between the corresponding component and the metal foam is exposed to less mechanical stresses by matching the thermal expansion coefficients of the metal foam and the component. In particular, this can make it possible for a sealing bond to be formed reliably and over a prolonged period of time between the metal foam and the component.
The object is furthermore achieved by a component in which molecules of C and/or molecules of B and N, which have a spherical or tubular structure, are contained in the metal foam used. This is because these molecules are suitable in the manner indicated above for physically or chemically binding a carrier gas which is then contained in the pores of the metal foam. Specifically, in the manner described above, the substances of the blowing agent are bound to the molecules, and the carrier gas which has formed the pores of the metal foam is released by a heat treatment.
According to an advantageous embodiment of the component, it is formed as a housing structure comprising a material which is different to the metal foam and comprises a cavity having an opening, which is closed by the metal foam. Hermetic sealing of the cavity is advantageously possible in this case, since an intimate bond is formed between the metal foam and the housing structure in the region of the opening. In particular when the metal foam is matched in terms of its thermal expansion coefficient to that of the housing structure in the manner indicated above, hermetic sealing can advantageously be ensured over a prolonged period of time even when the component is thermally stressed. This is particularly advantageous when the cavity is formed by a glass body, in particular a lamp.
A component having a housing structure 11 according to
Not represented is the possibility of providing further layers, which consist of materials having a negative thermal expansion coefficient, in the composite. For example, ZrW2O5, ZrV2O7, Sc2W3O12, Y2W3O12, K5Zr(PO4)2 or KzR2(PO4)3 are known as such materials.
In the right-hand half of the representation according to
The value of the concentration of pores 17 in the metal foam 18 depends on the concentration of the blowing agent. In
In the case of the housing structure 11 according to
According to
According to
| Number | Date | Country | Kind |
|---|---|---|---|
| 10 2010 022 598.3 | May 2010 | DE | national |
This application is a U.S. National Stage Application of International Application No. PCT/EP2011/058178 filed May 19, 2011, which designates the United States of America, and claims priority to DE Patent Application No. 10 2010 022 598.3 filed May 31, 2010. The contents of which are hereby incorporated by reference in their entirety.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2011/058178 | 5/19/2011 | WO | 00 | 11/29/2012 |
