Abstract
The commercial carbonyl iron powder coated with iron phosphate (20 wt.%) was dried (60°C for 2 h in air), calcinated at 400°C for 3 h in air, compacted at 600 MPa into cylindrical samples and subsequently sintered at 820, 900 and 1110°C for 30 min in N2-10%H2 atmosphere. By means of EDX and XRD analyses the phase composition of the coating and sintered microstructure was studied. Microstructure resulting from sintering at 820 and 900°C was formed by initial iron particles surrounded with the crystalline FePO4 and α-Fe2O3 phases. Due to liquid phase sintering at 1110°C a mixed microstructure containing spheroidized α-Fe phase surrounded by solidified liquid phase consisting of iron oxides and phosphorous compounds has been formed. In order to prepare a network composite microstructure the compacts based on spherical iron particles size of 100-160 µm coated with 2 wt.% of iron phosphate were dried, calcined at 400°C, compacted and liquid phase sintered at 980°C.
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