SHS Preparation and β-Irradiation Stability of Sr-Doped Graphite

2014 ◽  
Vol 563 ◽  
pp. 112-118
Author(s):  
Si Jin Su ◽  
Yi Ding ◽  
Xi Rui Lu

In order to study the treatment of simulated radioactive graphite contains 90Sr by SHS and its β-irradiation stability, waste forms were prepared in accordance with the reaction 3C + 4Al + 3TiO2 = 2Al2O3 + 3TiC+Q, by self-designed SHS equipment. Then the β-ray irradiation experiments were done at dose of 106Gy to evaluate its radiation resistance. The phase composition and morphology of the prepared waste forms before and after irradiation were characterized by X-ray diffractometer (XRD) and scanning electron microscope (SEM). The XRD results indicated that the major composition of the waste forms were Al2O3, TiC, C, TiO2 and AlN after reaction in atmosphere, and the SrO solid solubility could be up to 8wt%. It was found that the surface morphology of waste forms were mostly plate-shaped and mainly in about 10μm. The structure and microscopic morphology of waste forms didn't change significantly before and after irradiation according to the XRD spectra, SEM photos. Moreover, the calculated cell parameters results suggested that the lattice parameters of the main phase (TiC, Al2O3) changed about 10-3~10-2nm after irradiation, and the degree of changes in cell volume was about 10-4~10-3nm3 magnitude. The simulated 90SrO–containing radioactive graphite waste forms showed a certain β-ray radiation resistance.

2021 ◽  
pp. 1-6
Author(s):  
Mariana M. V. M. Souza ◽  
Alex Maza ◽  
Pablo V. Tuza

In the present work, LaNi0.5Ti0.45Co0.05O3, LaNi0.45Co0.05Ti0.5O3, and LaNi0.5Ti0.5O3 perovskites were synthesized by the modified Pechini method. These materials were characterized using X-ray fluorescence, scanning electron microscopy, and powder X-ray diffraction coupled to the Rietveld method. The crystal structure of these materials is orthorhombic, with space group Pbnm (No 62). The unit-cell parameters are a = 5.535(5) Å, b = 5.527(3) Å, c = 7.819(7) Å, V = 239.2(3) Å3, for the LaNi0.5Ti0.45Co0.05O3, a = 5.538(6) Å, b = 5.528(4) Å, c = 7.825(10) Å, V = 239.5(4) Å3, for the LaNi0.45Co0.05Ti0.5O3, and a = 5.540(2) Å, b = 5.5334(15) Å, c = 7.834(3) Å, V = 240.2(1) Å3, for the LaNi0.5Ti0.5O3.


MRS Advances ◽  
2018 ◽  
Vol 3 (56) ◽  
pp. 3323-3328
Author(s):  
Barys Korzun ◽  
Anatoly Pushkarev

ABSTRACTAlloys of the CuAlS2 – CuFeS2 system were prepared by thermobaric treatment at high pressure of 5.5 GPa and temperatures ranging from 573 to 1573 K and phase formation in the system was investigated using X-ray powder diffraction, optical microscopy and scanning electron microscopy equipped with energy dispersive spectroscopy. The unit-cell parameters (the lattice constants and the unit-cell volume) were computed as a function of the composition. Absence of complete solubility in the (CuAlS2)1-x-(CuFeS2)x system was established. Formation of solid solutions with the tetragonal structure of chalcopyrite was detected for compositions with the molar part of CuFeS2 x not exceeding 0.10.


2017 ◽  
Vol 12 (1) ◽  
pp. 63-77 ◽  
Author(s):  
Siriporn Sirikingkaew ◽  
Nuta Supakata

This study presents the development of geopolymer bricks synthetized from industrial waste, including fly ash mixed with concrete residue containing aluminosilicate compound. The above two ingredients are mixed according to five ratios: 100:0, 95:5, 90:10, 85:15, and 80:20. The mixture's physico-mechanical properties, in terms of water absorption and the compressive strength of the geopolymer bricks, are investigated according to the TIS 168-2546 standard. Scanning electron microscopy (SEM) and X-ray diffraction (XRD) analyses are used to investigate the microstructure and the elemental and phase composition of the brick specimens. The results indicate that the combination of fly ash and concrete residue represents a suitable approach to brick production, as required by the TIS 168–2546 standard.


2021 ◽  
Vol 1016 ◽  
pp. 1790-1796
Author(s):  
Maxim Syrtanov ◽  
Egor Kashkarov ◽  
Tatyana Murashkina ◽  
Nahum Travitzky

This paper describes the influence of sintering temperature on phase composition and microstructure of paper-derived Ti3AlC2 composites fabricated by spark plasma sintering. The composites were sintered at 100 MPa pressure in the temperature range of 1150-1350 °C. Phase composition and microstructure were analyzed by X-ray diffraction and scanning electron microscopy, respectively. The multiphase structure was observed in the sintered composites consisting of Ti3AlC2, Ti2AlC, TiC and Al2O3 phases. The decomposition of the Ti3AlC2 phase into Ti2AlC and TiC carbide phases was observed with temperature rise. The total content of Ti3AlC2 and Ti2AlC phases was reduced from 84.5 vol.% (1150 °C) to 69.5 vol.% (1350 °C). The density of composites affected by both the content of TiC phase and changes in porosity.


Materials ◽  
2019 ◽  
Vol 12 (24) ◽  
pp. 4171 ◽  
Author(s):  
Paweł Rutkowski ◽  
Jan Huebner ◽  
Adrian Graboś ◽  
Dariusz Kata ◽  
Dariusz Grzybek ◽  
...  

In this study, the influence of the addition of rare earth oxides on the phase composition and density of KNN piezoelectric ceramics was investigated. The initial powders of Na2CO3 and K2CO3 were dried at 150 °C for 2 h. Then, a powder mixture for synthesis was prepared by adding a stoichiometric amount of Nb2O5 and 5 and 10 wt % overabundance of Na2CO3. All powders were mixed by ball-milling for 24 h and synthesized at 950 °C. The phase composition of the reaction bed was checked by means of X-ray diffraction (XRD). It had an appearance of tetragonal and monoclinic K0.5Na0.5NbO3 (KNN) phases. Then, 1 and 2 wt % of Er2O3 and Yb2O3, were added to the mixture. Green samples of 25 mm diameter and 3 mm thickness were prepared and sintered by hot pressing at 1000 °C for 2 h under 25 MPa pressure. The final samples were investigated via scanning electron microscopy (SEM)-energy-dispersive X-ray spectroscopy (EDS), XRD, Rietveld, and ultrasonic methods. Phase analysis showed tetragonal and orthorhombic KNN phases, and a contamination of (K2CO3·1.5H2O) was present. The obtained KNN polycrystals had a relative density above 95%. Texturing of the material was confirmed as a result of hot pressing.


2018 ◽  
Vol 163 ◽  
pp. 05008
Author(s):  
Anna Skawińska

This paper presents the results of the studies carried out in the model systems and concerning the tobermorite synthesis with an addition of metahalloysite. Quartz sand and quicklime were the main raw material constituents. The mixtures in the form of slurries underwent hydrothermal treatment with an addition of metahalloysite (5%, 10%, 15%, 20% and 30%) for 4 hours and 12 hours. The resultant composites were analysed for their phase composition using X-ray powder diffraction. The microstructure was examined using the Scanning Electron Microscope. Tobermorite was the principle reaction product. When 30% metahalloysite was added to the mixture containing CaO and SiO2, the formation of katoite was found.


2012 ◽  
Vol 465 ◽  
pp. 76-79 ◽  
Author(s):  
Shuang Zhan ◽  
Xia Li

The novel Y2O3 nanoflowers were synthesized through a facile hydrothermal method without using any catalyst or template. The phase composition and the microstructure of as-prepared products were characterized by field emission scanning electron microscope (FE-SEM), X-ray diffraction (XRD) as well as Fourier transform infrared spectrum. The formation mechanism for the Y2O3 flowers has been proposed.


2008 ◽  
Vol 368-372 ◽  
pp. 977-979
Author(s):  
Sheng Li Jin ◽  
Ya Wei Li ◽  
Jing Liu ◽  
Yuan Bing Li ◽  
Lei Zhao ◽  
...  

AlN/Al ceramic composite was fabricated by directed melt nitridation of pure Al block covered with 10wt% Mg powder at 1300°C in a high purity flowing N2. Microstructure and phase composition of the composite were investigated by scanning electron microscopy with energy dispersive spectroscopy and X-ray diffraction. Results showed that AlN is the main phase in the composite and its lattice parameters of a and c are 3.1110Å and 4.9806Å, respectively. The phase composition of the composite changes along the growth direction and a gradient sandwich structure forms. The surface of the composite is made up of a dense and thin nodular AlN layer, underneath which an AlN/Al layer appears, followed by an AlN/Al/MgAl2O4 layer. Thermodynamic calculations predicted the formation of possible phases with the addition of Mg. It suggested that the content of Mg at the reaction frontier of nitridation is considerably lower to 0.15wt% where MgAl2O4 was stable, because of escape and reaction exhaustion of Mg. Once Mg is lower than 0.05wt%, only a dense AlN layer can exist, which prevents the further nitridation of Al melt.


2003 ◽  
Vol 807 ◽  
Author(s):  
A. G. Ptashkin ◽  
S. V. Stefanovsky ◽  
S. V. Yudintsev ◽  
S. A. Perevalov

ABSTRACTPu-bearing zirconolite and pyrochlore based ceramics were prepared by melting under oxidizing and reducing conditions at 1550 °C. 239Pu content in the samples ranged between ∼10 and ∼50 wt.%. Phase composition of the ceramics and Pu partitioning were studied using X-ray diffraction (XRD) and scanning electron microscopy with energy dispersive system (SEM/EDS). Major phases in the samples were found to be the target zirconolite and pyrochlore as well as a cubic fluorite structure oxide. Normally the Pu content in the Pu host phases was 10–12 wt.%. This corresponds to the Pu content recommended for matrices for immobilization of excess weapons plutonium. At higher Pu content (up to 50 wt.%) additional phases, such as a PuO2-based cubic fluorite-structured solid solution, perovskite, and rutile were found.


2009 ◽  
Vol 66 ◽  
pp. 171-174
Author(s):  
Zhao Deng ◽  
Ying Dai ◽  
Wen Chen

Single-crystalline BaTiO3 nanoparticles and BaCO3 nanowires were synthesized respectively through the use of a reverse micelle as a medium in the same Oleic acid/n-octane/H2O system, by changing the H2O2 dosage. Both the phase composition and the morphology can be controled. The samples derived were characterized with X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and high-resolution transmission electron microscopy (HRTEM). The formation mechanism has been fully discussed.


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