Carmen Galassi
National Research Council
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Featured researches published by Carmen Galassi.
Physical Review B | 2010
F. Cordero; F. Craciun; F. Trequattrini; E. Mercadelli; Carmen Galassi
The complex elastic compliance and dielectric susceptibility of
Journal of The European Ceramic Society | 2001
E. Roncari; Carmen Galassi; Floriana Craciun; Claudio Capiani; A Piancastelli
{({\text{Na}}_{0.5}{\text{Bi}}_{0.5})}_{1\ensuremath{-}x}{\text{Ba}}_{x}{\text{TiO}}_{3}
Journal of Applied Physics | 2012
Marco Deluca; Laurentiu Stoleriu; Lavinia Curecheriu; Nadejda Horchidan; Adelina Ianculescu; Carmen Galassi; Liliana Mitoseriu
(NBT-BT) have been measured in the composition range between pure NBT and the morphotropic phase boundary included,
Journal of The European Ceramic Society | 1997
R. Greenwood; E. Roncari; Carmen Galassi
0\ensuremath{\le}x\ensuremath{\le}0.08
Journal of Applied Physics | 2013
Cristina Elena Ciomaga; Alexandra Neagu; Mihai Valentin Pop; Mirela Airimioaei; Sorin Tascu; Giorgio Schileo; Carmen Galassi; Liliana Mitoseriu
. The compliance of NBT presents sharp peaks at the rhombohedral/tetragonal and tetragonal/cubic transitions, allowing the determination of the tetragonal region of the phase diagram, up to now impossible due to the strong lattice disorder and small distortions and polarizations involved. In spite of ample evidence of disorder and structural heterogeneity, the R-T transition remains sharp up to
Journal of The European Ceramic Society | 2001
Anna Luisa Costa; Carmen Galassi; G. Fabbri; E. Roncari; Claudio Capiani
x=0.06
Journal of Materials Research | 2001
Stefano Guicciardi; Carmen Galassi; Elena Landi; Anna Tampieri; K. Satou; Giuseppe Pezzotti
, whereas the T-C transition merges into the diffuse and relaxorlike transition associated with broad maxima of the dielectric and elastic susceptibilities. An attempt is made at relating the different features in the anelastic and dielectric curves to different modes of octahedral rotations and polar cation shifts. The possibility is also considered that the cation displacements locally have monoclinic symmetry, as for PZT near the morphotropic phase boundary.
Journal of the Acoustical Society of America | 1999
Stefano Marselli; Vittorio Pavia; Carmen Galassi; E. Roncari; Floriana Craciun; Guido Guidarelli
Piezoelectric porous lead zirconate titanate (PZT) ceramics prepared by different methods have been examined from a microstructural point of view. The effect of polymer volume and properties and sintering temperature on microstructure of samples and on their physical properties has been investigated. The wide range of pore volumes and pore size distributions was obtained by three different procedures: (a) reduction of the sintering temperature of the die pressed PZT samples; (b) use of a different forming technique like tape casting, starting from slurries with high volume of organic content; (c) addition of different volume concentrations of organic polymer to the PZT powder. It has been found that varying process parameters like quantity of polymer and sintering temperature changes both final porosity as well as pore size distribution, introducing dispersion in physical property values. The differences between the microstructural aspect of samples prepared by different methods and their influence on the physical properties of the samples are presented and discussed.
Journal of The European Ceramic Society | 1997
Carmen Galassi; E. Roncari; C. Capiani; Paola Pinasco
BaSnxTi1−xO3 solid solutions with compositions in the range x = 0–0.20 were studied by combining analysis of the field-induced dielectric and ferroelectric properties with Raman spectroscopic investigations. By combining techniques, the detection of specific features related to the ferroelectric-to-relaxor crossover with increasing Sn content is possible. Detailed tunability analysis of the x = 0.05 composition indicated that multiple components contribute to the dc-field induced permittivity response; these components are active in different temperature and field ranges and could be assigned to a few polarization mechanisms. First order reversal curves (FORC) for the material clearly show a transition from ferroelectric-to-relaxor behavior with increasing x, confirming the conclusions from the Raman and dielectric studies. This was evidenced by the shift of the FORC distribution over coercivities toward zero field values. Raman measurements allow the identification of the separate phases with varying Sn ...
Applied Physics Letters | 2012
Leontin Padurariu; Lavinia Curecheriu; Carmen Galassi; Liliana Mitoseriu
Abstract Aqueous suspensions suitable for the tape casting of alumina were produced, such that ceramic bodies with very high final sintered densities were obtained (100% of theoretical). This enables high purity, smooth, substrates to be produced without using environmentally damaging solvents. To prevent competitive adsorption of the binder with the dispersant, which leads to an increase in the viscosity and in the elastic modulus of the suspension, the binder was mixed very slowly for a short time in a ball mill. In the presence of the binder the optimum amount of dispersant was 0.3 mg m −2 (dry weight basis). These suspensions were not thixotropic. The minimum amount of binder required to produce a flexible, robust tape was established from tape casting experiments, as was the minimum amount of binder required to produce a tape that did not crack on drying. All suspensions were cast with both blades set at a gap of 0.4 mm and a Mylar tape speed of 20 cm min −1 ; the removal of air bubbles was achieved by exposing the slip to a vacuum for a few minutes. The final sintered density could be correlated directly with the volume fraction of powder (at a fixed binder content) and directly with the binder content (at fixed volume fraction). Sintering the discs revealed a greater shrinkage in the thickness direction than laterally owing to the non-spherical nature of the particles. However no correlation could be found between the thickness of the green body after casting/drying and the suspension viscosity.