Alpha-Decay Effects in 241Am-Doped Gadolinium Zirconate

2012 ◽  
Vol 1444 ◽  
Author(s):  
S.V. Stefanovsky ◽  
A.G. Ptashkin ◽  
S.V. Yudintsev ◽  
B.F. Myasoedov
Keyword(s):  
Heat Treatment ◽  
Relative Intensity ◽  
Alpha Decay ◽  
Fluorite Structure ◽  
Lattice Parameter ◽  
Oxide Mixture ◽  
Xrd Pattern ◽  
Gadolinium Zirconate ◽  
Main Reflection ◽  
Higher Doses

ABSTRACTSample of zirconate ceramic with a composition corresponding to formula Gd1.7241Am0.3Zr2O7 was synthesized by heat-treatment of mechanically activated and compacted in pellet oxide mixture at 1500 °C for 30 min. The d values on XRD pattern of the sample soon after synthesis (D = 7.9×1015 α-decays/g or 0.001 dpa) demonstrated fluorite structure with the most intensive peak with d111 =3.042 Å (a = 5.269 Å) and very weak diffuse reflections due to d-pyrochlore. At a dose of 7.9×1017 α-decays/g or 0.11 dpa the reflections were broadened by approximately 20% and their relative intensity slightly reduced. At higher doses all the weak superstructure reflections disappeared and the growth in intensity and narrowing of the main reflection occurred. Lattice parameter a increased with the dose and reached 5.343 Å (d111 = 3.085 Å) at a dose of 4.6×1018 α-decays/g or 0.42 dpa. At a dose of 5.5×1018 α-decays/g or 0.78 dpa positions of reflections were shifted to lower d-spaces (d111 value reduced to 3.071 Å) and the half-width of the major reflection was 67% of initial. For the 241Am-doped Gd-zirconate the structure recovery rate exceeds disordering rate and no amorphization occurred at doses higher than ∼0.2-0.3 dpa.

EFFECT OF HEAT TREATMENT ON THE STRUCTURE OF SiC−Si3N4 COMPOSITE ULTRAFINE POWDER

1996 ◽  
Vol 03 (01) ◽  
pp. 79-83 ◽  
Author(s):  
X. LI ◽  
Y. NAKATA ◽  
H. NAGAI ◽  
T. OKUTANI ◽  
M. SUZUKI
Keyword(s):  
Heat Treatment ◽  
Particle Size ◽  
Lattice Parameter ◽  
Ultrafine Powder ◽  
Phase Reaction ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
Transmission Electron ◽  
Heat Treated ◽  
Original Powder

Effect of heat treatment on the structure of SiC−Si3N4 composite ultrafine powder was studied. SiC-Si3N4 composite ultrafine powder synthesized by laser-induced gas-phase reaction was heat-treated at various temperatures below 1773 K in 99% Ar +1% H2 gas mixture. The change of the structure was studied by chemical analysis, x-ray diffraction (XRD), and transmission electron microscope (TEM). The structure of the powder did not change significantly in lattice constant, particle size, and composition by the treatment up to 1573 K . The structure of the powder changed drastically by the treatment above 1673 K . The broad XRD pattern due to β- Si for the original powder changed to the four phases of β- SiC , Si and α, β- Si 3N4 by the treatment at 1773 K , accompanied by large increases in particle size and lattice parameter, and decreases in nitrogen content and specific surface area.

High-Temperature Instability of A Cr2Nb-Nb(Cr) Microlaminate Composite

1996 ◽  
Vol 54 ◽  
pp. 374-375
Author(s):  
M. Larsen ◽  
R.G. Rowe ◽  
D.W. Skelly
Keyword(s):  
Heat Treatment ◽  
Solid Solution ◽  
High Temperature ◽  
Elevated Temperatures ◽  
Aircraft Engine ◽  
Lattice Parameter ◽  
Microstructural Stability ◽  
Elevated Temperature Strength ◽  
Cross Sectional ◽  
Bcc Structure

Microlaminate composites consisting of alternating layers of a high temperature intermetallic compound for elevated temperature strength and a ductile refractory metal for toughening may have uses in aircraft engine turbines. Microstructural stability at elevated temperatures is a crucial requirement for these composites. A microlaminate composite consisting of alternating layers of Cr2Nb and Nb(Cr) was produced by vapor phase deposition. The stability of the layers at elevated temperatures was investigated by cross-sectional TEM.The as-deposited composite consists of layers of a Nb(Cr) solid solution with a composition in atomic percent of 91% Nb and 9% Cr. It has a bcc structure with highly elongated grains. Alternating with this Nb(Cr) layer is the Cr2Nb layer. However, this layer has deposited as a fine grain Cr(Nb) solid solution with a metastable bcc structure and a lattice parameter about half way between that of pure Nb and pure Cr. The atomic composition of this layer is 60% Cr and 40% Nb. The interface between the layers in the as-deposited condition appears very flat (figure 1). After a two hour, 1200 °C heat treatment, the metastable Cr(Nb) layer transforms to the Cr2Nb phase with the C15 cubic structure. Grain coarsening occurs in the Nb(Cr) layer and the interface between the layers roughen. The roughening of the interface is a prelude to an instability of the interface at higher heat treatment temperatures with perturbations of the Cr2Nb grains penetrating into the Nb(Cr) layer.

Phase selection in precursor-derived yttrium aluminum garnet and related Al2O3–Y2O3 compositions

2005 ◽  
Vol 20 (4) ◽  
pp. 1017-1025 ◽  
Author(s):  
Ashutosh S. Gandhi ◽  
Carlos G. Levi
Keyword(s):  
Heat Treatment ◽  
Yttrium Aluminum Garnet ◽  
Lattice Parameter ◽  
Defect Structures ◽  
X Ray Diffraction ◽  
Phase Selection ◽  
X Ray ◽  
Yttrium Aluminum ◽  
Rich Side ◽  
Nitrate Solutions

Al2O3–Y2O3 powders were synthesized in the range of 25–55% Y2O3 by reverse coprecipitation of nitrate solutions. All starting powders were amorphous and formed primary yttrium aluminum garnet (YAG) upon crystallization. X-ray diffraction detected only garnet in compositions of 30–40% Y2O3 after heat treatment at 1250 °C. Compositions of 45–55% Y2O3 established a metastable YAG + Y4Al2O9 microstructure. The YAG phase field was metastably extended away from its stoichiometry, as indicated by a systematic increase in lattice parameter with Y2O3 content. Although some Al2O3 enrichment was achieved, YAG appears to tolerate greater off-stoichiometry on the Y2O3-rich side. Possible defect structures accommodating the solubility extension were examined. Phase selection results indicate that compositional inhomogeneity is not the only reason behind the appearance of hexagonal YAlO3, which is frequently reported during YAG synthesis.

The Kinetics of Ordering in Gadolinium Zirconate: an Unusual Oxygen Ion Conductor

1995 ◽  
Vol 398 ◽  
Author(s):  
Sossina M. Haile ◽  
Scott Meilicke
Keyword(s):  
Impedance Spectroscopy ◽  
Pyrochlore Structure ◽  
Fluorite Structure ◽  
Transformation Kinetics ◽  
X Ray Diffraction ◽  
Ion Conductor ◽  
Gadolinium Zirconate ◽  
X Ray ◽  
Oxygen Ion ◽  
Kinetics Of

ABSTRACTGadolinium zirconate, Gd2Zr2O7, undergoes an order-disorder transition at ∼1550°C, transforming from a defect fluorite structure (Fm3m) to a pyrochlore structure (Fd3m). Both cations and anions are ordered in the low-temperature, pyrochlore structure. In order to understand the interplay between anion and cation order parameters and ordering rates, the transformation kinetics of Gd2Zr2O7 have been examined via X-ray diffraction. Gadolinium zirconate is of particular interest because the oxygen ion conductivity of the ordered phase is significantly greatly than that of the disordered phase, in contrast to virtually every other known solid electrolyte. This difference in conductivity has provided a second technique for characterizing the transformation kinetics: in situ A.C. impedance spectroscopy. Results of the X-ray diffraction showed the growth of superstructure peak intensity to follow an apparent (time)½ dependence, rather than that expected from a nucleation and growth model. The impedance spectroscopy measurements, on the other hand, showed the conductivity to increase linearly with time. These results suggest the transition is second order in nature.

scholarly journals Studies on Structural and Morphological Properties of Multidoped Ceria Ce0.8Nd0.0025Sm0.0025Gd0.005Dy0.095Y0.095O2-δ(x=0.2) as Solid Solutions

2016 ◽  
Vol 2016 ◽  
pp. 1-9 ◽  
Author(s):  
Marija Stojmenović ◽  
Maja C. Pagnacco ◽  
Vladimir Dodevski ◽  
Jelena Gulicovski ◽  
Milan Žunić ◽  
...  
Keyword(s):  
Raman Spectroscopy ◽  
Solid Solutions ◽  
Room Temperature ◽  
Oxygen Vacancies ◽  
Room Temperature Ferromagnetism ◽  
Fluorite Structure ◽  
Lattice Parameter ◽  
Morphological Properties ◽  
Fluorite Type ◽  
Potential Improvement

The nanopowdery solid solutions of multidoped ceria Ce0.8Nd0.0025Sm0.0025Gd0.005Dy0.095Y0.095O2-δ(x=0.2) with the fluorite type crystal structure of CeO2were synthesized for the first time. Two synthesis procedures were applied: the modified glycine-nitrate procedure (MGNP method) and room temperature self-propagating reaction (SPRT method). All nanopowders were characterized by XRPD analysis, Raman spectroscopy, low temperature nitrogen physisorption, TEM, and SEM methods. According to the XRPD and Raman spectroscopy results, single phase solid solutions of fluorite structure were evidenced regardless of the number of dopants and synthesis procedure. Both XRPD and TEM were analyses evidenced nanometer particle dimensions. The SPRT method results in obtaining sample with higher specific surface area, smaller crystallite and particles sizes, and the same values of the lattice parameter in comparison to pure CeO2. Raman spectroscopy was confirmed to the oxygen vacancies introduced into the ceria lattice when Ce4+ions were replaced with cations (dopants) of lower valence state (3+), which may indicate the potential improvement of ionic conductivity. Additionally, the presence of oxygen vacancies in the lattice ceria, as well as very developed grain boundaries, gives a new possibility for potential application of obtained nanopowders in the area of room temperature ferromagnetism as spintronics.

scholarly journals Effects of Li2O additive on structural, magnetic and electrical properties of Ni-Mg ferrite

2014 ◽  
Vol 38 (1) ◽  
pp. 7-18 ◽  
Author(s):  
Sheikh Mohi Uddin Rumy ◽  
Mahabub Alam Bhuiyan ◽  
MH Mesbah Ahmed ◽  
Kazi Hanium Maria ◽  
MA Hakim ◽  
...  
Keyword(s):  
Electrical Properties ◽  
Spinel Ferrite ◽  
Lattice Parameter ◽  
Initial Permeability ◽  
Dielectric Behavior ◽  
Ferromagnetic Behavior ◽  
Xrd Pattern ◽  
Dielectric Constant Measurement ◽  
Academy Of Sciences ◽  
Magnetic And Electrical Properties

The effects of Li2O additives on the structural, magnetic and electrical properties of Ni0.5Mg0.5Fe2O4, prepared by conventional double sintering ceramic technique were investigated. The X-raydiffraction (XRD) pattern of the prepared samples showed single phase cubic spinel structure.Variation of lattice parameter has been observed with the variation of Li2O content. Theenhancement of bulk density has been observed for 2 mol% Li2O additive, but further increase inLi2O concentration, these values decrease. Enhancement of initial permeability (??) have beenobserved for the sample with 2 mol% Li2O additives while it decreases for higher concentration ofLi2O. The Curie temperature is found to decrease with the increase in Li2O additive. The resistivityincreases with increasing additive content and showed a significant dispersion with frequency,which is the normal ferromagnetic behavior. The dielectric constant (??) measurement showed thenormal dielectric behavior of spinel ferrite. Possible explanation for the observed features arediscussed. DOI: http://dx.doi.org/10.3329/jbas.v38i1.20198 Journal of Bangladesh Academy of Sciences, Vol. 38, No. 1, 7-18, 2014

Direct Preparation of Ce0.8Sm0.2O1.9 Powders Oxidized With H2O2 for Low Temperature SOFCs Application

2005 ◽  
Author(s):  
Jianbing Huang ◽  
Zongqiang Mao ◽  
Bin Zhu ◽  
Lizhai Yang ◽  
Ranran Peng ◽  
...  
Keyword(s):  
Single Phase ◽  
Fluorite Structure ◽  
X Ray Diffraction ◽  
Composite Electrolyte ◽  
Xrd Pattern ◽  
Transmission Electron ◽  
Direct Preparation ◽  
Novel Method ◽  
Power Densities

A novel method was developed to prepare fine doped ceria (DCO) powders directly. Ceria doped with 20 mol. % of samarium (Ce0.8Sm0.2O1.9, SDC) was prepared by in-situ oxidization of hydroxide precipitates with H2O2 in the solutions. The resultant powder desiccated at 85°C overnight was characterized by X-ray diffraction (XRD), thermogravimetry /differential thermal analysis (TG/DTA), and transmission electron microscopy (TEM). The XRD pattern showed that the as-dried SDC powder is single phase with a cubic fluorite structure like that of pure CeO2. An anode-supported SOFC was also fabricated based on SDC and 20wt. % (62mol. %Li2CO3–38 mol. %K2CO3) composite electrolyte, LiNiO2 as cathode and NiO as anode, by cold pressing. Using hydrogen as the fuel and air as the oxidant, the I-V and I-P characteristics exhibit excellent performances and the maximum power densities are about 696, 469, 377 and 240 mWcm−2 at 650, 600, 550 and 500°C, respectively.

Self-Radiation Damage in Actinide Host Phases of Nuclear Waste Forms

1984 ◽  
Vol 44 ◽  
Author(s):  
W. J. Weber ◽  
J. W. Wald ◽  
Hi. Matzke
Keyword(s):  
Radiation Damage ◽  
Nuclear Waste ◽  
Amorphous State ◽  
Alpha Decay ◽  
Ceramic Materials ◽  
Thermal Recovery ◽  
Radiation Induced ◽  
Crystalline Ceramic ◽  
Higher Doses ◽  
Nuclear Waste Forms

AbstractThree crystalline ceramic materials, which occur as host phases for the long-lived actinides in many nuclear waste formulations, were doped with Cm-244, and the effects of self-radiation damage from alpha decay on microstructure and physical properties were investigated. The irradiation-induced microstructure consisted of individual amorphous tracks from both the alpha-recoil particles and the spontaneous fission fragments. The eventual overlap of the tracks at higher doses leads to a completely amorphous state. This radiation-induced amorphization process results in measured increases in volume, leachability, and stored energy. Thermal recovery of the radiation-induced swelling and amorphization occurs with full recrystallization to the initial structures.

Effect of Heat Treatment on TiNx Film Structure

2005 ◽  
Vol 480-481 ◽  
pp. 187-192
Author(s):  
S. Zerkout ◽  
M. Benkahoul ◽  
H. Sahraoui ◽  
S. Achour ◽  
A. Mosser
Keyword(s):  
Heat Treatment ◽  
Nitrogen Content ◽  
Thermal Instability ◽  
Lattice Parameter ◽  
Film Structure ◽  
High Nitrogen Content ◽  
High Nitrogen ◽  
Tin Films ◽  
Film Instability ◽  
Nitrogen Contents

TiN films with different nitrogen contents were deposited on glass and Si (100) substrates by d. c. magnetron reactive sputtering. The structure of the films was determined by Xray diffraction. It was found that heat treatment at 773 decreased the lattice parameter. A considerable thermal instability of over-stoichiometric films was observed after annealing films in air. This instability enhanced with increasing nitrogen content and is characterized by an abundant appearance of clear and dark disks in Scanning Electron Microscopy (SEM). Also, it was shown that the film instability does not come from an interfacial reaction but was observed when the TiNx layers present a (200) preferred orientation together with high nitrogen content.

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