A PZT niobium doped material (PZTN) was developed from precursor powders obtained by spray drying of a water solution of Zr and Pb nitrates, Ti isopropoxide and Nb-ammonium complex. The thermo - oxidative process as well as the phase evolution were analysed. The morphology of powders were investigated as a funtction of the spray drying conditions. The stoichiometry of the systems was checked at each stage of the process and no fluctuation was detected. The obtained powders had a spherical, hollow and porous structure and were transformed into a pure perovskite phase at 550 °C. The samples, sintered at 1100°C for 2h in air showed 98% relative density at a densification T 100°C lower than following the conventional mixed oxide route1. The green and final densities were improved introducing a grinding step and high pressure cold isostatic consolidation. Some sintered samples were fully densified by hot isostatic pressing (1100°C, 300 bars) post-treatment, obtaining pore free structures. The electrical characterization showed comparable or better properties than those obtained with the mixed oxide method.
PZT Material by Spray Drying: from powder synthesis to electromechanical properties / F. Bezzi; A. L. Costa; D. Piazza; A. Ruffini; S. Albonetti; C. Galassi. - In: JOURNAL OF THE EUROPEAN CERAMIC SOCIETY. - ISSN 0955-2219. - STAMPA. - 25 (13):(2005), pp. 3323-3334. [10.1016/j.jeurceramsoc.2004.08.027]
PZT Material by Spray Drying: from powder synthesis to electromechanical properties
BEZZI, FEDERICA;ALBONETTI, STEFANIA;
2005
Abstract
A PZT niobium doped material (PZTN) was developed from precursor powders obtained by spray drying of a water solution of Zr and Pb nitrates, Ti isopropoxide and Nb-ammonium complex. The thermo - oxidative process as well as the phase evolution were analysed. The morphology of powders were investigated as a funtction of the spray drying conditions. The stoichiometry of the systems was checked at each stage of the process and no fluctuation was detected. The obtained powders had a spherical, hollow and porous structure and were transformed into a pure perovskite phase at 550 °C. The samples, sintered at 1100°C for 2h in air showed 98% relative density at a densification T 100°C lower than following the conventional mixed oxide route1. The green and final densities were improved introducing a grinding step and high pressure cold isostatic consolidation. Some sintered samples were fully densified by hot isostatic pressing (1100°C, 300 bars) post-treatment, obtaining pore free structures. The electrical characterization showed comparable or better properties than those obtained with the mixed oxide method.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.