Advanced Materials Research
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Vols. 29-30
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Vols. 26-28
Vols. 26-28
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Vols. 20-21
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Vols. 15-17
Advanced Materials Research Vols. 26-28
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Paper Title Page
Abstract: The effect of hydrostatic pressure mechanically applied to hydride on the equilibrium
hydrogen gas pressure and temperature have been examined theoretically. From free energy
calculations where elastic energy is taken into account, equilibrium gas pressure and temperature
increases and decreases with increasing applied compressive stress, respectively. In the case of
magnesium hydride, equilibrium temperature decreases to 63 °C at the hydrogen gas pressure being 1
atom when volume expansion at hydriding is perfectly suppressed by an external compressive stress.
The temperature is remarkably lower than that obtained by alloying various elements.
217
Abstract: The temperature dependence of single-crystal elastic constants of L10-ordered
single-crystals of FePd . A complete set of elastic constants has been determined with the resonance
ultrasound spectroscopy technique. The compounds clearly show a tetragonal elastic anisotropy, c11 <
c33 and c44 < c66. The temperature dependencies of the anisotropies are not simply explained by the
variation of axial ratio (c/a) of the crystal.
221
Abstract: Electrochemical properties and microstructure evolution during lithiation and delithiation
of Ni3Sn2 single crystals with the hexagonal B82-type related ordered structure have been studied as a
function of the crystal orientation by charge/discharge tests, powder X-ray diffraction and
transmission electron microscopy. Charge and discharge capacities are strongly dependent on the
crystal orientation. When the surface of the thin plate anode is perpendicular to the basal plane of the
parent B82 unit cell, the capacities are approximately twice as high as those for the sample whose
surface is parallel to the basal plane, which is considered to be related to the difference in the diffusion
behavior of lithium with respect to the crystal orientation.
225
Abstract: Manganese-alloyed Ru2Si3-based alloys with various alloy compositions have been
prepared and the phase relationships of these alloys have been investigated as a function of the Mn
concentration using X-ray powder diffraction, scanning electron microscopy and transmission
electron microscopy. A series of Ru1-xMnxSiy chimney-ladder phases is confirmed to be formed over a
wide compositional range (x ≥0.12). These chimney-ladder phases are considered to be formed to
stabilize the HT-Ru2Si3 chimney-ladder phase through the substitution of Ru with Mn. The
compositions of the chimney-ladder phases are, however, significantly deviated from the idealized
composition satisfying the valence electron concentration rule: VEC=14.
229
Abstract: The present paper reports the results of microcreep tests and microstructure of alloy 617
foils of 100μm thick specimens at 800 and 900 oC in air. Before each test, the specimens were
annealed in vacuum at 950 oC for 17 hrs. The dynamic recrystallizations were observed during
creep test. The voids and cracks were observed along grain boundaries. The maximum elongation of
grains was found at the lowest applied stress along the loading direction. The average grain size
decreases from 20 μm to 2 μm as applied stress increases from 48 to 120 MPa at 800 oC and from
50 μm to 5 μm as the applied stress increases from 35 to 60MPa at 900 oC. The steady state creep
rates were increased as applied stress increased in all the specimens.
233
Abstract: Textured SrBi2Nb2O9 (SBN) ceramics were fabricated by templated grain growth (TGG)
method. The plated-like SBN particles with shape anisotropy prepared by molten salt method were
used as the templates. The SBN powders prepared by conventional solid (CS) reaction were used as
matrix powders. It was found that the textured SBN ceramics can be obtained by TGG method. The
grain orientation (Lotgering factor, f) increased with the increase of sintering temperature and content
of the templates. The textured SBN ceramics with f=0.86 could then be obtained after sintering at
1300 °C for 3 h with 20wt.% templates. The relative density keeps rising with increasing temperature
until it reaches a peak value 91.22% at the sintering temperature 1300°C, after which it decreases.
239
Abstract: BaBi4-xLaxTi4O15 (BBLT) ceramics were prepared by conventional solid phase sintering
ceramics processing technology. The crystal structure and the microstructure were detected by X-ray
diffraction (XRD) and scanning electron microscope (SEM). The XRD analyses show that La3+ ions
doping did not change the crystal structure of BBT ceramics. The sintering temperature increased
from 1120°C to 1150°C with increasing Lanthanum content from 0 to 0.5, but it widened the sintering
temperature range from 20°C to 50°C and refined the grain size of the BBT ceramic. Additionally,
polarization treatment was performed and finally piezoelectric property was measured. As a result,
the piezoelectric constant d33 of the 0.1at.% doped BBLT ceramics reached its highest value about
22pc/N at polarizing electric field of 8kV/mm and polarizing temperature of 120°C for 30min.
243
Abstract: Bismuth titanate was prepared from the sol-gel method. Bismuth nitrate and titanium
isopropoxide were used as the starting precursors with the mole ratio of Bi:Ti as 4:3. Solutions were
mixed in acetic acid medium and heat at 80 oC for 2h. Sols were obtained after adjusting the final of
pH of solution to 2. Gels were formed after drying at 100 oC for 24h. The milled powders were
calcined at 500-800 oC for 2h. The phase formation was investigated by X-ray diffractometry
(XRD). Single phase with orthorhombic structure of bismuth titanate was obtained after calcination
at 700 oC for 2h. The morphology and chemical composition were studied by scanning electron
microscopy (SEM) and energy dispersive spectroscopy (EDS). The average particle size was 0.50-
1.5 μm with the irregular shape. The elemental composition of bismuth, titanium and oxygen
showed the characteristic X-ray energy values.
247
Abstract: TiB2-TiC ceramic matrix composites were fabricated by in situ synthesis under hot
isostatic pressing (HIP) with 3TiH2-B4C and 11TiH2-3B4C being the raw materials, respectively. The
XRD analysis indicates that the samples synthesized from 3TiH2-B4C have TiB2 and TiC phases,
while those from 11TiH2-3B4C have not only TiB2 and TiCx phases, but also Ti3B4 phase. TiB2-TiCx
ceramic matrix composites obtained from 11TiH2-3B4C have better mechanical properties than those
from 3TiH2-B4C. The microstructures of the composites are investigated with SEM and TEM. TiB2
grains are platelet grains; Ti3B4 grains have two different morphologies. Ti3B4 phases are formed
through two different paths: fine grain Ti3B4 is formed through TiB+B=Ti3B4 at low temperature;
large plate-like grain Ti3B4 is formed through TiB2+TiB=Ti3B4 at high temperature.
251
Preparations and Characterizations of Perovskite PMN Ceramics by Using a One-Step Calcination Method
Abstract: A relaxor ferroelectric material, Pb(Mg1/3Nb2/3)O3 (PMN) powder with a pyrochlore-free
phase, was prepared by using a one-step calcinations method. The pyrochlore phase was prevented by
coating Mg(OH)2 on Nb2O5 particles. Pure-perovskite PMN powder was synthesized by a single
calcination of the coating powder mixed with appropriate amounts of PbO at 900 oC for 2 h. The
pyrochlore-free perovskite PMN powders were sintered to 96.9% density at 1100 oC. The sintered
PMN ceramics exhibited a dielectric constant maximum of ~11 700 at room temperature at a
frequency of 1 kHz.
255