USRE45658EExpiredUtility

Method of manufacturing amorphous metallic foam

48
Assignee: SCHROERS JANPriority: Jan 17, 2003Filed: Jan 20, 2004Granted: Aug 25, 2015
Est. expiryJan 17, 2023(expired)· nominal 20-yr term from priority
C22C 1/087C22C 1/085C22C 1/086B22D 25/005B22D 27/13C22C 1/08B22F 2998/00B22F 2999/00
48
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References
29
Claims

Abstract

Metallic foams comprising high viscosity materials and apparatuses and methods of manufacturing such foams, and more particularly methods for controllably manufacturing metallic foams from bulk-solidifying amorphous alloys are provided.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. A method of manufacturing a metallic foam from a bulk-solidifying amorphous alloy comprising:
 providing a molten bulk-solidifying amorphous alloy; 
 introducing a plurality of gas bubbles, to the molten alloy at a temperature about the liquidus temperature of the alloy to form a precursor at a first pressure such that the bubbles are formed with a specified internal bubble pressure; 
 holding the conditions of the precursor after introduction of the plurality of gas bubbles steady for a specified period of time such that a proportion of the plurality of bubbles above a chosen size threshold are removed from the molten precursor via flotation such that the bubble size distribution within the precursor is at least partially homogenized; 
 at least partially cooling the precursor to a processing temperature below the nose of the crystallization curve of the alloy and above the glass transition temperature of the alloy at a cooling rate such that the molten alloy substantially maintains its amorphous state; and 
 expanding the bubbles in the precursor while the precursor is at the processing temperature by providing a pressure gradient to the precursor where the pressure during the expansion is lower than the internal bubble pressure of the introduced gas bubbles formed during the precursor forming step. 
 
     
     
       2. The method of  claim 1 , further comprising quenching the expanded precursor after expanding the bubbles, where the quenching is conducted at a cooling rate such that the at least a partial amorphous atomic structure is formed in the metallic foam object. 
     
     
       3. The method according to  claim 1 , wherein the precursor is cooled to below the glass transition temperature sufficiently fast to form a solidified precursor material with substantially amorphous atomic structure, and further comprising heating the solid precursor material into the super-cooled region of the bulk-solidifying amorphous alloy above the glass transition temperature of the alloy and below the nose of the crystallization curve of the alloy to expand the bubbles. 
     
     
       4. The method according to  claim 1 , wherein the temperature of the precursor is reduced to within the supercooled region of the bulk solidifying amorphous alloy during cooling sufficiently fast to avoid any substantial crystallization. 
     
     
       5. The method according to  claim 1 , wherein the gas bubbles are mechanically generated in the molten alloy. 
     
     
       6. The method according to  claim 1 , wherein the gas bubbles are introduced to the molten alloy through in gas form through a nozzle. 
     
     
       7. The method according to  claim 1 , wherein the gas bubbles are introduced to the molten alloy by adding an a gas releasing agent to the molten alloy. 
     
     
       8. The method according to  claim 1 , wherein a volume fraction of <30% of the plurality of bubbles have sizes between 1 μm and 1 mm. 
     
     
       9. The method according to  claim 1 , wherein at least 50% by volume of the metallic foam has an amorphous atomic structure. 
     
     
       10. The method according to  claim 1 , further including regulating the process parameters during the expansion in accordance with a calculated size dependent flotation velocity of the bubbles as given by the equation:
   V sed =2a 2 [ρl−ρ g ]g/9ρ
 
 
       to control the homogeneity, size and volume distribution of the bubbles in the precursor. 
     
     
       11. The method according to  claim 1 , wherein the step of introducing gas bubbles to form the precursor occurs at a pressure of about 50 bar or more. 
     
     
       12. The method according to  claim 1 , wherein the precursor is maintained within a temperature range such that the precursor has a viscosity of about 10 6  Pa·s to 10 12  Pa·s during the expanding step. 
     
     
       13. The method according to  claim 1 , wherein the expansion of the precursor is carried out in one of either a mold or a cast. 
     
     
       14. The method according to  claim 1 , wherein the bubbles of the metallic foam have a size distribution of from about 1 μm to about 10 μm. 
     
     
       15. The method according to  claim 1 , wherein the bulk solidifying amorphous alloy is a Zr-base amorphous alloy. 
     
     
       16. The method according to  claim 1 , wherein the bulk solidifying amorphous alloy has a ΔT of at least 60° C. 
     
     
       17. The method according to  claim 1 , wherein the bulk solidifying amorphous alloy is an Fe-base amorphous alloy. 
     
     
       18. The method according to  claim 1 , wherein the plurality of bubbles is one of either close or open celled. 
     
     
       19. A method comprising:
 introducing gas bubbles to an alloy in a molten form at a temperature about a liquidus temperature of the alloy at a first pressure to form a precursor;   removing a proportion of the gas bubbles above a chosen size threshold such that a size distribution of the bubbles within the precursor is at least partially homogenized;   cooling at least a portion of the precursor such that the alloy substantially maintains an amorphous state; and   expanding the bubbles in the precursor to form a foam comprising the alloy substantially in the amorphous state.   
     
     
       20. The method of claim 19, further comprising quenching the expanded precursor after expanding the bubbles, where the quenching is conducted at a cooling rate such that an at least partially amorphous atomic structure is formed in the metallic foam object. 
     
     
       21. The method according to claim 19, wherein the precursor is cooled to below the glass transition temperature sufficiently fast to form a solidified precursor material with a substantially amorphous atomic structure, and further comprising heating the solid precursor material into the super-cooled region of the bulk-solidifying amorphous alloy above the glass transition temperature of the alloy and below the nose of the crystallization curve of the alloy to expand the bubbles. 
     
     
       22. The method according to claim 19, wherein the gas bubbles are introduced to the molten alloy by adding a gas releasing agent to the molten alloy. 
     
     
       23. The method according to claim 19, wherein the bubbles have a size distribution of from about 1 μm to about 10 μm. 
     
     
       24. The method according to claim 19, wherein the bulk solidifying amorphous alloy is a Zr-based amorphous alloy or a Fe-based amorphous alloy. 
     
     
       25. The method of claim 19, wherein the precursor has a pore size distribution of between 1 μm and 10 μm. 
     
     
       26. The method of claim 25, wherein the pore size distribution is homogeneous. 
     
     
       27. The method of claim 19, wherein the precursor comprises less than 30% by volume of gas bubbles below a chosen size threshold such that a size distribution of the bubbles within the precursor is substantially homogeneous. 
     
     
       28. The method of claim 19, wherein the precursor comprises metallic foam. 
     
     
       29. The method of claim 28, wherein the metallic foam has a smaller casting thickness than the bulk-solidifying amorphous alloy without any bubbles.

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