Effects of Milling Time and Annealing Schedule on Mechanical Activation Synthesis of Brownmillerite Structural Ca2Fe2O5

2011 ◽  
Vol 295-297 ◽  
pp. 1099-1102
Author(s):  
Fen Wang ◽  
Chun Zhao ◽  
Jian Feng Zhu
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Powder Diffraction ◽  
Milling Time ◽  
High Energy ◽  
Sem Analysis ◽  
Annealing Schedule ◽  
X Ray ◽  
Lower Temperature ◽  
Scanning Electron

The brownmillerite structural Ca2Fe2O5is successfully prepared by high energy milling starting from CaCO3and Fe2O3. The composition and transformation of phase and structure with different milling time and annealed at 800 °C for 24 h were characterized by the X-ray powder diffraction (XRD) and scanning electron microscopy (SEM) analysis. The results indicate that the high pure brownmillerite structural Ca2Fe2O5could be efficiently synthesized at lower temperature by the mechanically activated mixtures.

The Synthesis of Cu0.81Ni0.19 Intermetallics by Mechanical Alloying

2012 ◽  
Vol 496 ◽  
pp. 379-382
Author(s):  
Rui Song Yang ◽  
Ming Tian Li ◽  
Chun Hai Liu ◽  
Xue Jun Cui ◽  
Yong Zhong Jin
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Grain Size ◽  
Mechanical Alloying ◽  
Milling Time ◽  
Elemental Powder ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scherrer Equation ◽  
Scanning Electron

The Cu0.81Ni0.19 has been synthesized directly from elemental powder of nickel and copper by mechanical alloying. The alloyed Cu0.81Ni0.19 alloy powders are prepared by milling of 8h. The grain size calculated by Scherrer equation of the NiCu alloy decreased with the increasing of milling time. The end-product was analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM)

SYNTHESIS, MORPHOLOGY AND STRUCTURAL PROPERTIES OF (GD,ND)SR2RUCU2O8 SAMPLES

2003 ◽  
Vol 17 (04n06) ◽  
pp. 899-904 ◽  
Author(s):  
A. VECCHIONE ◽  
M. GOMBOS ◽  
C. TEDESCO ◽  
A. IMMIRZI ◽  
L. MARCHESE ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Solid State ◽  
Powder Diffraction ◽  
Solid State Reaction ◽  
X Ray ◽  
Structure And Morphology ◽  
Polycrystalline Powder ◽  
Scanning Electron

NdSr 2 RuCu 2 O x material has been prepared as polycrystalline powder by solid state reaction. The compound has been investigated by synchrotron x-ray powder diffraction and scanning electron microscopy. The experimental results show that the average crystal structure is a disordered cubic perovskite with Nd and Sr cations occupying the same site and the same substitution is found for Cu and Ru atoms. A comparison between the crystal structure and morphology of this compound and the superconducting tetragonal GdSr 2 RuCu 2 O 8 is also discussed.

Synthesis of PZT Disks by a Hydrothermal Method

2012 ◽  
Vol 174-177 ◽  
pp. 592-595
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Yu Jiang Wang ◽  
Xiao Feng Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Hydrothermal Method ◽  
Formation Mechanism ◽  
Powder Diffraction ◽  
Self Assembly ◽  
Hydrothermal Process ◽  
X Ray ◽  
Extended Length ◽  
Scanning Electron

The organization of nanostructures across extended length scales is a key challenge in the design of integrated materials with advanced functions. PbZr0.52Ti0.48O3multilayer disks which were constructed by oriented rectangle nanoparticles were easily prepared by a simple surfactant-free hydrothermal process. The as-prepared powders were characterized by X-ray powder diffraction (XRD) and scanning electron microscopy (SEM). The results indicated that the as-prepared PZT disks were constructed by self-assembly of rectangle nanoparticles by a perfect manner. The formation mechanism of the products was discussed.

Mechanochemical Synthesis of Intermetallic Compounds in the Gallium–Iridium System

2019 ◽  
Vol 18 (03n04) ◽  
pp. 1940067
Author(s):  
P. Vitiaz ◽  
N. Lyakhov ◽  
T. Grigoreva ◽  
E. Pavlov
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Mechanical Activation ◽  
Intermetallic Compounds ◽  
High Energy ◽  
Planetary Mill ◽  
X Ray Diffraction ◽  
X Ray ◽  
Active Liquid ◽  
Scanning Electron

The interaction between a solid inert metal Ir and an active liquid metal Ga during mechanical activation in a high-energy planetary mill is studied by X-ray diffraction and scanning electron microscopy with high-resolution energy dispersive X-ray microanalysis. The effect of mechanical activation on the formation of GaxIry intermetallic compounds and GaxIry/Ir composites and their solubility in acids was investigated. The subsequent extraction of Ga from intermetallic compounds and composites in the mixture of concentrated acids [Formula: see text] makes it possible to produce nanoscale Ir.

Polymer-Assisted Hydrothermal Synthesis of PbTiO3 Crystals

2012 ◽  
Vol 528 ◽  
pp. 176-179
Author(s):  
Yong Gang Wang ◽  
Lin Lin Yang ◽  
Xin Wang ◽  
Song Li ◽  
Yu Jiang Wang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Hydrothermal Synthesis ◽  
Formation Mechanism ◽  
Powder Diffraction ◽  
Self Assembly ◽  
Hydrothermal Process ◽  
X Ray ◽  
Assembly Structure ◽  
Scanning Electron

Using polymer as a surfactant, we successfully synthesized of PbTiO3 crystals with a self-assembly structure by a hydrothermal process. The as-obtained powders were characterized by X-ray powder diffraction (XRD) and scanning electron microscopy (SEM). The results show that the presence of PVP, PEG and PVA plays a key role on the formation of self-assembly structure and the corresponding formation mechanism was briefly discussed.

scholarly journals Preparation and Phase Relations in the CuSbSe2 – CuInSe2 System

2016 ◽  
Vol 1735 ◽  
Author(s):  
Barys V. Korzun ◽  
Valery R. Sobol ◽  
Marin Rusu ◽  
Ruben M. Savizky ◽  
Alena A. Fadzeyeva ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Optical Microscopy ◽  
Mole Fraction ◽  
Powder Diffraction ◽  
Room Temperature ◽  
Phase Relations ◽  
X Ray ◽  
Ternary Compounds ◽  
Scanning Electron

ABSTRACTThe CuInSe2 and CuSbSe2 ternary compounds and alloys of the (CuSbSe2)1-x·(CuInSe2)x system with the mole fraction of CuInSe2 (x) equal to 0.05, 0.15, 0.25, 0.375, 0.50, 0.625, 0.75, 0.85, and 0.95 were prepared and the phase relations in this system were investigated by X-ray powder diffraction, optical microscopy, and scanning electron microscopy. It was shown that the alloys of the CuSbSe2-CuInSe2 system are biphasic at room temperature in the whole range of compositions, and the limits of solubility for CuSbSe2 in CuInSe2 and for CuInSe2 in CuSbSe2 do not exceed 0.001 mole fraction.

Component of Cu/n-SiO2 Composite Particles by Mechanical Milling

2011 ◽  
Vol 299-300 ◽  
pp. 1320-1323
Author(s):  
Jian Hua Du ◽  
Xiao Hui Zheng ◽  
Xiao Ying Zhu
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Mechanical Milling ◽  
Milling Time ◽  
Composite Particles ◽  
Composite Powders ◽  
X Ray ◽  
Scanning Electron

Copper based composite powders with nano-SiO2 were prepared by mechanical milling technology. The effects of milling time on morphology and component of the composite particles were characterized by scanning electron microscopy (SEM) and energy disperse X-ray spectroscopy (EDS), respectively. Results showed that dendrite composite particles change to the flaky, and then to spherical ones with the milling time increasing. The n-SiO2 particles disperse more homogeneously in the composite particles with the milling time increasing.

Chemical Interaction of Phosphates MII2P4O12 with Melted MICl or MINO3 (MI – Li, Na, K; MII – Mg, Co, Ni, Zn)

2015 ◽  
Vol 230 ◽  
pp. 297-302 ◽  
Author(s):  
Oksana V. Livitska ◽  
Nataliya Yu. Strutynska ◽  
Igor V. Zatovsky ◽  
Nikolay S. Slobodyanik
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Ftir Spectroscopy ◽  
Powder Diffraction ◽  
Diffuse Reflectance ◽  
Chemical Interaction ◽  
Crystalline Phases ◽  
X Ray ◽  
Temperature Range ◽  
Scanning Electron

The interaction in the systemsMII2P4O12-MICl (MINO3) (MI– Li, Na, K;MII– Mg, Co, Ni, Zn) was investigated in temperature range 1073-673 K. The conditions of formation phosphates: Li3PO4,MIMIIPO4(MI– Na, K), Na4MII3(PO4)2P2O7, Na9Co3(PO4)5have been established. Obtained crystalline phases have been investigated using X-ray powder diffraction, Diffuse reflectance, Raman and FTIR spectroscopy and scanning electron microscopy methods.

The adsorption of methylene blue on montmorillonite from acid solutions

Clay Minerals ◽  
2011 ◽  
Vol 46 (3) ◽  
pp. 461-471 ◽  
Author(s):  
Z. Klika ◽  
P. Pustková ◽  
M. Dudová ◽  
P. Čapková ◽  
Ch. Kliková ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Methylene Blue ◽  
Ion Exchange ◽  
Powder Diffraction ◽  
Acid Solutions ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Adsorption Wave ◽  
Scanning Electron

AbstractThe adsorption of methylene blue (MB) on montmorillonite from acid solutions has not yet been studied in detail. In this paper the adsorption of this dye on Ca/SAz montmorillonite from 0.32, 0.80 and 1.60 M HCl solutions at ambient temperature and after 2 hours leaching was carefully studied and evaluated. Under the above conditions the MB/SAz intercalates formed are practically insoluble. In contrast to the adsorption of methylene blue on montmorillonite from aqueous solutions, the adsorption from acid solutions consists of two adsorption waves. The intercalated samples from the first and second waves were studied using X-ray powder diffraction (XRD), FTIR, Vis spectroscopy, and scanning electron microscopy (SEM) equipped with a microprobe system. The adsorption of MB in the first wave is attributed to ion exchange of the dye cationic species (MB+, MB22+, H-aggregates, MBH2+ and H+) for the original interlayer cations of montmorillonite. The percentages of MBH2+ and H+ based on total adsorbed MB were estimated for varying HCl concentrations. The second adsorption wave is linked to the precipitation of MB species on the outer MB/SAz surface.

X-ray powder diffraction data for two new compounds (NH4)1.5Ni2V2O7(OH)1.5 · H2O and (NH4)1.5Cu1.125Ni1.125V2O7(OH)2 · H2O

2011 ◽  
Vol 26 (S1) ◽  
pp. S51-S54
Author(s):  
Johana Arboleda ◽  
Adriana Echavarría
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Thermogravimetric Analysis ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Powder Diffraction Data ◽  
X Ray Diffraction ◽  
X Ray ◽  
New Compounds ◽  
Scanning Electron

Two new bimetallic and trimetallic compounds (NH4)1.5Ni2V2O7(OH)1.5 · H2O and (NH4)1.5Cu1.125 Ni1.125V2O7(OH)2 · H2O were synthesized by hydrothermal method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and X-Ray fluorescence (XRF). Crystallographic studies showed that both compounds are hexagonal with space group P-62c.

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