Light Burning Condition of Preparing Dolomite Clinker Using Natural Dolomite

2018 ◽  
Vol 281 ◽  
pp. 156-162
Author(s):  
Wang Nian Zhang ◽  
Xi Tang Wang ◽  
Zhou Fu Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Grain Size ◽  
Sintering Process ◽  
X Ray Diffraction ◽  
Burning Temperature ◽  
X Ray ◽  
Temperature Range ◽  
Scanning Electron

The influence of the light burning temperature on the sintering property of nature dolomite has been investigated by two-step sintering process in the temperature range 1500 °C to 1600 °C. The resulting bulk densities and apparent porosities of the sintered dolomite samples were examined, and analyzing the sintered dolomite by scanning electron microscopy and X-ray diffraction were performed. The results showed light burned at 850 °C for 3 h, the main phases of the dolomite with 3-5 grain size were MgO, CaO and little CaCO3, and then fired at 1600 °C,the density of sintering dolomite reached to 3.38 g/cm3, the apparent property was 1.2 %, the size of MgO grain up to 3.75 μm . However when dolomite light burned at 1050 °C for 3 h, the main phases were MgO and CaO, and then fired at 1600 °C,the density of sintering dolomite only was 3.30 g/cm3, the apparent property was 2.3 %, the size of MgO only was 3.05 μm .

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)

The Effects of Al-Ca Compounds on Grain Refinement of Mg-Ca Alloys

2011 ◽  
Vol 686 ◽  
pp. 348-354 ◽  
Author(s):  
Shu Tao Xiong ◽  
Fu Sheng Pan ◽  
Bin Jiang ◽  
Xiao Ke Li
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Grain Size ◽  
Grain Refinement ◽  
X Ray Diffraction ◽  
X Ray ◽  
Metallic Compound ◽  
Scanning Electron ◽  
Main Factor

In the present work, Al-Ca metallic compound was prepared in Mg-Ca alloys and the effects of Al-Ca metallic compound and different Al/Ca values on the grain refinement of Mg-Ca alloys were investigated by scanning electron microscopy and X-ray diffraction, and the mechanism of grain refinement of Mg-Ca alloys was discussed. The results showed that the grain size of Mg-0.5Ca alloy was obviously reduced from 550μm to 230μm due to the addition of Al. Al2Ca phase existed in these alloys and its morphology evolved from granular to rod-like. It is regarded as the main factor for the grain refinement.

Research on Friction and Wear Properties of Ti(C,N)/Fe Composites

2013 ◽  
Vol 650 ◽  
pp. 326-332
Author(s):  
Yang Li ◽  
Zhi Ping Sun ◽  
Rui Feng Wang ◽  
Li Yan Zou
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Friction And Wear ◽  
Adhesive Wear ◽  
Sintering Process ◽  
X Ray Diffraction ◽  
Wear Properties ◽  
X Ray ◽  
Friction And Wear Properties ◽  
Scanning Electron

The effect of different load, revolving speed ,content of Ti(C,N) and sintering process on the friction coefficient and wear rate of Ti(C,N)/Fe composites was investigated systemically. Besides, the wear morphology of Ti(C,N)/Fe composites were researched with an environment scanning electron microscopy(SEM),and the phase composition were studied by X-ray diffraction(XRD).The research shows that the wear mechanism of Ti(C,N)/Fe composites are abrasive wear and adhesive wear.

Grain Size Effect on Lattice of Ni Nanocrystals Prepared Through Polyol Method

2008 ◽  
Vol 8 (8) ◽  
pp. 4127-4131 ◽  
Author(s):  
G. S. Okram ◽  
Kh. Namrata Devi ◽  
H. Sanatombi ◽  
Ajay Soni ◽  
V. Ganesan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Atomic Force Microscopy ◽  
Grain Size ◽  
Polyol Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Force Microscopy ◽  
Atomic Force ◽  
Scanning Electron

Nanocrystalline nickel powders were prepared with grain size 'd' in the range 40–100 nm diameters through polyol method. X-ray diffraction (XRD), scanning electron microscopy (SEM) and atomic force microscopy (AFM) were used for characterization. XRD of the prepared samples consistently matched with standard fcc structure of nickel without any impurity peak. Detailed analysis and calculations using Scherrer equation for (111) peak revealed systematic increase in line width and peak shifting towards lower diffraction 2θ angles with decrease in nickel to ethylene glycol mole ratio. Different values of d estimated from various peaks of each sample suggested associated microstrains in the nanograins. Values of d estimated from X-ray diffraction patterns were compared with those obtained from atomic force microscopy and scanning electron microscopy results, and discussed. Observed lattice expansion is explained, on the basis of a theoretical model of linear elasticity.

scholarly journals Chemical and Wetting Analysis of the Ni-Ti Coating on SiC Improved by a 2-Step Coating-Sintering Process

Materials ◽  
2020 ◽  
Vol 13 (22) ◽  
pp. 5235
Author(s):  
Yang Liu ◽  
Ying-Xin Wang ◽  
Qiang Yang ◽  
Fu Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Sintering Process ◽  
X Ray Diffraction ◽  
Control Groups ◽  
X Ray ◽  
Surface Energies ◽  
Metal Ceramic ◽  
Sintering Conditions ◽  
Scanning Electron

A two-stepped coating-sintering process to prepare the qualified Ni–Ti transition applied in metal-ceramic bonding proved to be effective to improve the wetting abilities. The method was introduced in detail and compared with 2 control groups. To analyze the benefits, the morphology and composition were captured by field emission scanning electron microscopy (FE-SEM), energy dispersive spectroscopy (EDS), and X-ray diffraction (XRD). The comparisons of different coating depths and different sintering conditions were also recorded and analyzed. The influence of the EDS detecting depth was a concern in the discussions. Finally, the contact angle tests and surface energies were also estimated to verify the reliability of the transition layer. The results indicated that the coating-sintering process combined with protective sintering was preferred and necessary to increase the activeness.

Effect of Ti and Sb Elements Addition on the Microstructure and Corrosion Resistance of Hot-Dip Galvanized Zn-11Al-3Mg Alloy

2021 ◽  
Vol 1035 ◽  
pp. 630-637
Author(s):  
Hui Jie Sun ◽  
Guo Rong Zhou ◽  
Ming Ming Zhang ◽  
Xue Feng Wang ◽  
Shui Yu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Grain Size ◽  
Corrosion Resistance ◽  
Energy Dispersive Spectrometry ◽  
X Ray Diffraction ◽  
Rich Phase ◽  
X Ray ◽  
Pitting Corrosion Resistance ◽  
Scanning Electron

The effect of Ti and Sb elements addition on the microstructures and corrosion resistance of hot-dip galvanized Zn-11Al-3Mg alloy was investigated by scanning electron microscopy (SEM) equipped with energy dispersive spectrometry (EDS), X-ray diffraction (XRD) and Electrochemical workstation, respectively. Results showed that the grain size of the alloy was obviously refined with the addition of Ti and Sb elements, due to Al3Ti phase as the nucleation substrate resulted in the transformation of Al-rich phase from dendrite to petal-like. In addition, the pitting corrosion resistance of the alloy has been significantly enhanced.

scholarly journals Structural properties of the composites (BaFe12O19/Ni0.3Cu0.2Zn0.5Al-0.5Fe1.5O4) prepared by sol-gel auto combustion

2019 ◽  
Vol 24 (4) ◽  
pp. 69
Author(s):  
Mohammed Mustafa Rashid1 ◽  
Sabah J. Fathi2 ◽  
Rafea A. Munef ◽  
Bilal Omer Ahmed1
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Grain Size ◽  
Sol Gel ◽  
Structural Features ◽  
Nano Composites ◽  
X Ray Diffraction ◽  
X Ray ◽  
Auto Combustion ◽  
Scanning Electron

The nanocomposites ferrites (BaFe12O19/Ni0.3Cu0.2Zn0.5Al­0.5Fe1.5O4) with (x=10,25,50,75,90%) were prepared by sol-gel auto combustion. The micro-structural features of the samples were studied using X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. The results were compared which show that the grain size of the nano composites which prepared by sol-gel auto combustion about (25-46) nm.   http://dx.doi.org/10.25130/tjps.24.2019.075  

Impedance Spectroscopy of Nanocrystalline Y-Stabilized Tetragonal Zirconia

1997 ◽  
Vol 500 ◽  
Author(s):  
P. Mondal ◽  
H. Hahn
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Grain Size ◽  
High Resolution ◽  
Impedance Spectroscopy ◽  
Grain Boundaries ◽  
Tetragonal Zirconia ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

ABSTRACTImpedance Spectroscopy, X-Ray Diffraction and High Resolution Scanning Electron Microscopy have been used to study the effect of extremely fine grain size on electrical properties such as dc-conductivity and activation energies in nanocrystalline Y-stabilized tetragonal zirconia. The samples were prepared from powders produced by the Inert Gas condensation method. X-Ray Diffraction was used to characterize phase and average grain size of the sample. In addition, grain size and microstructure of the sample was examined using High Resolution Scanning Electron Microscopy. With Impedance Spectroscopy relaxations of O−2-ions in the lattice and in the grain boundaries could be resolved. The dc-conductivities of the lattice and the grain boundaries were deduced from the data. The activation energies for ac- and dc-conductivity of the lattice and grain boundary relaxation are reported.

Study of 4.5%mol Y2O3-Doped ZrO2 with Submicrometer Grain Size

2014 ◽  
Vol 805 ◽  
pp. 570-575
Author(s):  
Eleomar Lena ◽  
Adriana Scoton Antonio Chinelatto ◽  
Adilson Luiz Chinelatto
Keyword(s):  
Electron Microscopy ◽  
Activation Energy ◽  
Scanning Electron Microscopy ◽  
Grain Size ◽  
Electrical Properties ◽  
Pechini Method ◽  
Oxygen Flow ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

The aim of this study was to obtain 4.5%mol Y2O3-doped ZrO2dense with submicrometer grain size and studying the effects of using oxygen flow during calcination in the electrical properties of bodies sintered. The powders were synthesized by the Pechini method. After synthesis, the resins were dried and the calcinations were performed in air and in oxygen flow at 600°C for 2 h. The powders were pressed with 1600 MPa and sintered by Two Step Sintering (TSS) at 1500°C / 5 min and 1200°C, 1300oC, 1400°C, remaining at these temperatures for 2 and 10 hours. The sinterized samples were characterized by X-ray diffraction, apparent density, scanning electron microscopy and impedance spectroscopy. The apparent densities were greater than 94% for all conditions of calcination and sintering. The value of the activation energy was 0.7eV for the grain and 0.9 eV for the grain boundaries.

scholarly journals Nanostructure of Crystal Hydroxyapatite from Fluorosis: Affected Enamel

2011 ◽  
Vol 2 (4) ◽  
pp. 321-325
Author(s):  
Abdillah Imron Nasution
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Grain Size ◽  
Surface Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
The Stability ◽  
Scanning Electron

ABSTRACT Fluorosis is a condition due to ingestion of excessive amounts of fluor which can cause the change the teeth structure and strength. Currently, a little explanation was available to describe the surface and change of nanostructure crystal hydroxyapatite which contribute to influence the macrocharacteristic of fluorosis enamel. Aims and objectives To describe the change of surface structure, c-axis, a-axis and grain size of crystal hydroxyapatite on fluorosis enamel. Materials and methods This research was carried out the fluorosis and normal enamel specimen by using scanning electron microscopy/ energy disperse X-ray (SEM/EDX) to determine fluor concentration and the surfaces structure of fluorosis enamel, and powder X-ray diffraction (XRD) to determine change of c- and a-axis of hydroxyapatite of fluorosis enamel. Results Fluor concentration were higher in fluorosis enamel and the surface increasingly roughness and porous. SEM/EDX also confirmed gaps areas between enamel rods and visible aprismatic zone in some regions. The axis on fluorosis enamel was a-axis = 9.3786 Å and c-axis = 6.8836 Å. The a-axis on normal enamel was = 9.4148 Å and c-axis = 6.8791 Å. Grain size of fluorosis enamel was 19.59 nm and normal enamel was 20.30 nm. Conclusion Fluor as most electronegative element changes the c-axis, a-axis, and grain size of crystal hydroxyapatite and generates the internal atomic bonding which influences the stability of enamel strength.

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