cessed by a spark plasma sintering method. Therefore, it is worthwhile to investigate the microstructure and mechanical properties of aluminum foam processed by spark plasma sintering. In the present paper, microstructure and compressive properties of an aluminum foam processed by spark plasma sintering are compared with those of an aluminum foam processed by electric furnace sintering. Commercially available aluminum powder (purity = 99.9%, powder size < =3 µm) was used as a starting material. Sodium chloride (NaCl) particles with a spheroidal shape (mean size = 520 µm) were prepared as the space-holding material. The weight ratio of the aluminum powder to the space-holding powder was determined, for the required porosity, to be 80%. Fig. 1 shows the schematic illustration of processing of an aluminum foam by spark plasma sintering. The process consisted of four steps; mixing, pressing, sintering and leaching. First, the aluminum powder and the spaceholding powder were thoroughly blended in an agate mortar. After the ingredients were homogeneously mixed, the mixed powder was uniaxially pressed in a carbon die at a pressure of 20 MPa. Then, spark plasma sintering was conducted at 773 K with a pressure of 20 MPa for 5 min by using an on-off pulsed DC voltage. The sintered specimen was placed into a running hot water bath to leach out the imbedded NaCl particles, leaving behind the aluminum foam with porous structure. A scanning electron micrograph of the aluminum foam processed by spark plasma sintering is shown in Fig. 2. It can be seen that completely interconnected networks of cell edges were formed and the space-holding particles were leached out. Sintering in an electric furnace was carried out for comparison with spark plasma sintering. For the sintering in the electric furnace, the mixed powder was uniaxially pressed in a steel mold at a pressure of