Multi-stage pore development in Ag foams by the reduction of Ag2O and CuO mixtures. (15th January 2020)
- Record Type:
- Journal Article
- Title:
- Multi-stage pore development in Ag foams by the reduction of Ag2O and CuO mixtures. (15th January 2020)
- Main Title:
- Multi-stage pore development in Ag foams by the reduction of Ag2O and CuO mixtures
- Authors:
- Atwater, Mark A.
Fudger, Sean J.
Nelson, Christopher B.
Hornbuckle, B.Chad
Knauss, Steven J.
Brennan, Samuel A.
Darling, Kristopher A. - Abstract:
- Abstract: Pore expansion in solid metals is typically driven by an entrapped gas phase, such that temperature directly determines both the pressure within the pores and the ability of the matrix to plastically deform. This approach fundamentally limits the total porosity, as all pores are active simultaneously, which quickly results in coalescence and percolation. The method introduced here converts dispersed oxide particles to a gaseous reactant using reduction, such that independent stages of pore formation and expansion can be achieved by using more than one oxide chemistry. This is demonstrated using silver and copper oxides distributed within a silver matrix. As the temperature is raised, the silver oxide reduces first and creates porosity. As the temperature is raised further, the copper oxide reduces and creates additional porosity. This allows the pore morphology and grain size to be uniquely controlled while still maintaining the simplicity and scalability of the process. The microstructural development is studied through a combination of isothermal annealing, optical dilatometry, and focused ion beam cross-sectioning, and implications and strategies for other alloy systems are discussed. Graphical abstract: Image 1 Highlights: Pore expansion in metals is limited by coalescence and percolation. Pores can be created through the reduction of dispersed oxides. Multiple oxide types can be used to separate foaming temperatures. Higher porosity and finer microstructureAbstract: Pore expansion in solid metals is typically driven by an entrapped gas phase, such that temperature directly determines both the pressure within the pores and the ability of the matrix to plastically deform. This approach fundamentally limits the total porosity, as all pores are active simultaneously, which quickly results in coalescence and percolation. The method introduced here converts dispersed oxide particles to a gaseous reactant using reduction, such that independent stages of pore formation and expansion can be achieved by using more than one oxide chemistry. This is demonstrated using silver and copper oxides distributed within a silver matrix. As the temperature is raised, the silver oxide reduces first and creates porosity. As the temperature is raised further, the copper oxide reduces and creates additional porosity. This allows the pore morphology and grain size to be uniquely controlled while still maintaining the simplicity and scalability of the process. The microstructural development is studied through a combination of isothermal annealing, optical dilatometry, and focused ion beam cross-sectioning, and implications and strategies for other alloy systems are discussed. Graphical abstract: Image 1 Highlights: Pore expansion in metals is limited by coalescence and percolation. Pores can be created through the reduction of dispersed oxides. Multiple oxide types can be used to separate foaming temperatures. Higher porosity and finer microstructure can be achieved using multiple oxides. … (more)
- Is Part Of:
- Materials & design. Volume 186(2020)
- Journal:
- Materials & design
- Issue:
- Volume 186(2020)
- Issue Display:
- Volume 186, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 186
- Issue:
- 2020
- Issue Sort Value:
- 2020-0186-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-01-15
- Subjects:
- Porous metals -- Solid state foaming -- Mechanical alloying -- Dilatometry -- Microstructure -- Grain boundary pinning
Materials -- Periodicals
Engineering design -- Periodicals
Matériaux -- Périodiques
Conception technique -- Périodiques
Electronic journals
620.11 - Journal URLs:
- http://catalog.hathitrust.org/api/volumes/oclc/9062775.html ↗
http://www.sciencedirect.com/science/journal/02641275 ↗
http://www.sciencedirect.com/science/journal/02613069 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.matdes.2019.108273 ↗
- Languages:
- English
- ISSNs:
- 0264-1275
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5393.974000
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