scholarly journals Improving the Optical Properties of Potassium Chloride Crystals by Doping Diamond Nanoparticles

2021 ◽  
Author(s):  
Hamid Reza Dehghanpour ◽  
Mahsa Shabani
Keyword(s):  
Potassium Chloride ◽  
Glow Curve ◽  
Czochralski Method ◽  
Xrd Analysis ◽  
Crystal Form ◽  
X Ray Diffraction ◽  
X Ray ◽  
Diamond Nanoparticles ◽  
Infra Red

Abstract In this work, the growth and characterization of potassium chloride crystals containing diamond nanoparticles has been performed. The crystals were grown by the Czochralski method and the doped samples contained 0.5, 1 and 1.5% impurities of diamond nanoparticles. The crystals were characterized by X ray diffraction (XRD), Fourier transform infra-red spectroscopy (FTIR), scanning electron microscopy (SEM), etching and thermoluminesence (TL). The XRD analysis shows the most of the nanodiamonds are still in single crystal form. FTIR demonstrates the composed crystals are transparent in IR range (transmission ~ 87%). The etching analysis reveals a crystal dislocation in order of 105 for the samples. Examination of thermoluminescence properties of crystals by gamma irradiation with doses of 10, 80 and 300 Gy showed that the sample with 0.5% doped ND had the best glow curve, but for the dose of 1000 Gy, the sample with 1% doped had the best curve.

Effect of expandable and expanded graphites on the thermo-mechanical properties of polyamide 11

2018 ◽  
Vol 51 (2) ◽  
pp. 175-190 ◽  
Author(s):  
F Oulmou ◽  
A Benhamida ◽  
A Dorigato ◽  
A Sola ◽  
M Messori ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Xrd Analysis ◽  
Crystal Form ◽  
X Ray Diffraction ◽  
Polyamide 11 ◽  
X Ray ◽  
Diffraction Peaks ◽  
Graphite Composites ◽  
And Storage

The preparation and thermo-mechanical characterization of composites based on polyamide 11 (PA11) filled with various amounts of both expandable and expanded graphites are presented. Investigation conducted using X-ray diffraction (XRD), scanning electron microscopy and surface area analyses indicated how graphite expanded under the selected processing conditions. The XRD analysis on PA11/graphite composites revealed no change in the crystal form of the PA11, while the presence of diffraction peaks associated to the graphite-stacked lamellae can be still detected. All the investigated composites showed an improvement of the thermal stability and mechanical properties (elastic and storage moduli).

scholarly journals Identification and Characterization of Maitara Island Clay, North Maluku

2021 ◽  
Vol 328 ◽  
pp. 01002
Author(s):  
Deasy Liestianty ◽  
Muliadi ◽  
Marhan ◽  
Said Hi Abbas ◽  
Yanny
Keyword(s):  
Clay Minerals ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
Sem Images ◽  
X Ray ◽  
Oxide Component ◽  
Infra Red ◽  
Main Component ◽  
Identification And Characterization

Characterization and identification of Maitara Island clay have been carried out. This study aims to determine the types of minerals contained in the Maitara Island clay. The analytical methods used include X-Ray Fluorescence (XRF) to determine the chemical composition of Maitara Island clay, X-Ray Diffraction (XRD) for mineralogical analysis of Maitara Island clay, Fourier Transmission Infra Red (FTIR) to determine the types of vibrations that exist between the atoms in clay minerals from Maitara Island, and Scanning Electron Microscopy (SEM) to determine the morphology of clay minerals. XRF analysis showed that silica was the element found to dominate the clay minerals with a percentage of 40.79%. Moreover, the highest oxide component found was SiO2 with a percentage of 87.25%. XRD analysis indicated that the Maitara Island clay minerals are composed of montmorillonite, magmatite, aluminum oxide colondrum, cristobalite, lime, titanium oxide, and hematite. The results of FTIR analysis denoted the presence of silica as silanol and siloxane. SEM images showed angular grains which signified silica as the main component in the clay minerals of Maitara Island

A study on using expanded perlite with hydroxyapatite: Reinforced bio-composites

2021 ◽  
pp. 095441192199656
Author(s):  
Erdoğan Karip ◽  
Mehtap Muratoğlu
Keyword(s):  
Body Fluid ◽  
Xrd Analysis ◽  
Cold Isostatic Pressing ◽  
Expanded Perlite ◽  
X Ray Diffraction ◽  
Pressing Method ◽  
X Ray ◽  
Infra Red ◽  
Ft Ir

People are exposed to different kinds of diseases or various accidents in life. Hydroxyapatite (HA) has been widely employed for bone treatment applications. In this study, HA was extracted from sheep bones. Bio-composites were doped with 1, 5, and 10 wt.% of expanded perlite and 5 wt.% of ZrO2–MgO-P2O5. The bio-composites were prepared by the cold isostatic pressing method (250 MPa) and sintered at 900°C for 1 h. In order to evaluate the characteristics of the bio-composites, microhardness, density, X-ray diffraction (XRD), Fourier transform infra-red spectroscopy (FT-IR), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS) analyses were carried out on them. Additionally, the specimens whose characteristics were determined were kept in synthetic body fluid (SBF), and their in vitro behavior was examined. As a result, it was observed that microhardness increased as both the weight and the grain size of the expanded perlite were increased. Calcium silicate, tri-calcium phosphate, and hydroxyapatite were observed in the XRD analysis of all samples, and the formation of apatite structures was increased by addition of ZrO2–MgO–P2O5.

Characterization and A Preliminary Study of TiO2 Synthesis from Lampung Iron Sand

2020 ◽  
Vol 849 ◽  
pp. 113-118
Author(s):  
Yayat Iman Supriyatna ◽  
Slamet Sumardi ◽  
Widi Astuti ◽  
Athessia N. Nainggolan ◽  
Ajeng W. Ismail ◽  
...  
Keyword(s):  
Food Packaging ◽  
Xrd Analysis ◽  
Major Elements ◽  
Raw Material ◽  
Solid Residue ◽  
X Ray Diffraction ◽  
X Ray ◽  
Leaching Solution ◽  
Ti Content

The purpose of this study is to characterize Lampung iron sand and to conduct preliminary experiments on the TiO2 synthesis which can be used for the manufacturing of functional food packaging. The iron sand from South Lampung Regency, Lampung Province that will be utilized as raw material. The experiment was initiated by sieving the iron sand on 80, 100, 150, 200 and 325 mesh sieves. Analysis using X-Ray Fluorescence (XRF) to determine the element content and X-Ray Diffraction (XRD) to observe the mineralization of the iron sand was conducted. The experiment was carried out through the stages of leaching, precipitation, and calcination. Roasting was applied firstly by putting the iron sand into the muffle furnace for 5 hours at a temperature of 700°C. Followed by leaching using HCl for 48 hours and heated at 105°C with a stirring speed of 300 rpm. The leaching solution was filtered with filtrate and solid residue as products. The solid residue was then leached using 10% H2O2 solution. The leached filtrate was heated at 105°C for 40 minutes resulting TiO2 precipitates (powder). Further, the powder was calcined and characterized. Characterization of raw material using XRF shows the major elements of Fe, Ti, Mg, Si, Al and Ca. The highest Ti content is found in mesh 200 with 9.6%, while iron content is about 80.7%. While from the XRD analysis, it shows five mineral types namely magnetite (Fe3O4), Rhodonite (Mn, Fe, Mg, Ca) SiO3, Quart (SiO2), Ilmenite (FeOTiO2) and Rutile (TiO2). The preliminary experiment showed that the Ti content in the synthesized TiO2 powder is 21.2%. The purity of TiO2 is low due to the presence of Fe metal which is dissolved during leaching, so that prior to precipitation purification is needed to remove impurities such as iron and other metals.

The Characteristic Evaluation of Hydroxyapatite Powders Synthesized from CaCO3 Refined from Oyster Shell and H3PO4

2006 ◽  
Vol 118 ◽  
pp. 639-644
Author(s):  
Hye Sung Kim ◽  
Su Chak Ryu
Keyword(s):  
Bone Density ◽  
Inductively Coupled Plasma ◽  
Oyster Shell ◽  
Atomic Emission ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Inductively Coupled ◽  
Infra Red ◽  
Ft Ir

Hydroxyapatite (Ca10(PO4)6(OH)2, HAp) powders is synthesized using the mixed powders of CaCO3 refined from oyster shells and phosphoric acid (H3PO4-98%, Daejung) as starting materials. The characteristic evaluation and chemical analysis of the synthesized powders is performed by X-ray diffraction (XRD), Fourier-transformed infra-red spectroscopy (FT-IR), and inductively-coupled plasma atomic emission spectroscopy (ICPAES). XRD analysis of synthetic powder by heat treatment at 1300°C for 2hrs shows only HAp peaks corresponding to stoichiometric HAp. It is confirmed by ICP-AES test that impurities such as Zn, In, Ti, Ba, Cd, Pb, and Mn, is not detected at all, but small amounts of Ti and Be is observed (0.099ppm Ti and 0.002ppm Ba). Variation of bone density is measured by giving medication of HAp powder with drinking water into human body continuously for three month. After the medication, the bone density is higher than the medication before. This means that HAp powder made from this process can be used as improver of bone density.

Production and Characterization of HVOF Sprayed NiCr-TiC Coatings Using SHS Powder Feedstock

2000 ◽  
Author(s):  
M.T. Blatchford ◽  
A.J. Horlock ◽  
D.G. McCartney ◽  
P.H. Shipway ◽  
J.V. Wood
Keyword(s):  
Thermal Spraying ◽  
Xrd Analysis ◽  
Powder Size ◽  
Coating Properties ◽  
X Ray Diffraction ◽  
Hvof Spraying ◽  
X Ray ◽  
Wear Rates ◽  
Powder Feedstock

Abstract In this paper, the production of NiCr-TiC powder by SHS, suitable for HVOF spraying, is discussed together with results on the microstructure and coating properties. Compacts for SHS were prepared by mixing elemental Ti and C with pre-alloyed Ni-20wt.% Cr powder to give an overall composition of 35wt.% NiCr and 65wt.% TiC. These were then ignited and a self-sustaining reaction proceeded to completion. Reacted compacts were crushed, sieved, and classified to give feedstock powders in size ranges of 10-45 µm and 45-75 µm. All powder was characterized prior to spraying based on particle size distribution, x-ray diffraction (XRD), and scanning electron microscopy (SEM/EDS). Thermal spraying was performed using both H2 and C3H6 as fuel gases in a UTP/Miller Thermal HVOF system. The resulting coatings were characterized by SEM and XRD analysis, and the microstructures correlated with powder size and spray conditions. Abrasive wear was determined by a modified 'dry sand rubber wheel' (DSRW) test and wear rates were measured. It has been found that wear rates comparable to those of HVOF sprayed WC-17wt% Co coatings can be achieved.

Microstructural Characterization of Glass-to-Metal Brazed Joint

2012 ◽  
Vol 616-618 ◽  
pp. 1732-1735 ◽  
Author(s):  
Xi Hai Shen ◽  
Yu Gang Zheng ◽  
Liang Chang ◽  
Jin Jia Guo ◽  
Song Bin Ye ◽  
...  
Keyword(s):  
Thermal Power ◽  
Microstructural Characterization ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Solar Thermal Power ◽  
Brazed Joints ◽  
Brazed Joint ◽  
Scanning Electron

Aiming at the glass-to-metal seals serving in the Solar Thermal Power (STP), glass-to-metal vacuum brazed joints were studied. Scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis were performed to examine the microstructure and element contents of interface seam on the glass-to-metal vacuum brazed joints. Also, the compositional concentration of the interface seam was measured by using energy dispersive spectroscopy (EDS).

The Preparation and Characterization of LiFe0.98Ni0.01Nb0.01PO4/C by Carbon Reduction Route

2012 ◽  
Vol 581-582 ◽  
pp. 570-573
Author(s):  
Jia Feng Zhang ◽  
Bao Zhang ◽  
Xue Yi Guo ◽  
Jian Long Wang ◽  
He Zhang Chen ◽  
...  
Keyword(s):  
Carbon Coating ◽  
Xrd Analysis ◽  
Initial Discharge Capacity ◽  
X Ray Diffraction ◽  
Capacity Retention ◽  
X Ray ◽  
Carbon Reduction ◽  
Initial Discharge ◽  
Structure Morphology

The LiFe0.98Ni0.01Nb0.01PO4/C was synthesized by carbon reduction route using FePO4•2H2O as precursor. The LiFe0.98Ni0.01Nb0.01PO4/C sample was characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) and electrochemical measurements. The XRD analysis, SEM and TEM images show that sample has the good crystal structure, morphology and carbon coating. The charge-discharge tests demonstrate that the powder has the better electrochemical properties, with an initial discharge capacity of 164.6 mAh•g−1 at current density of 0.1 C. The capacity retention reaches 99.8% after 100 cycles at 0.1C.

Preparation and Characterization of Ce-Doped Ba0.2Sr0.8TiO3 Ferroelectric Ceramics

2010 ◽  
Vol 97-101 ◽  
pp. 1091-1096
Author(s):  
Dong Fang Han ◽  
Qun Tang ◽  
Qing Meng Zhang ◽  
Lei Wang ◽  
Ju Du
Keyword(s):  
Dielectric Constant ◽  
Xrd Analysis ◽  
Ferroelectric Ceramics ◽  
X Ray Diffraction ◽  
X Ray ◽  
Structure And Property ◽  
Dielectric Constant And Loss ◽  
Ce Content ◽  
Doping Ratio

The structure and property of Ce-doped Ba0.2Sr0.8TiO3 (BST) were investigated as a function of Ce content. The density experiment results confirmed that increasing the Ce doping ratio caused the decrease in shrinkage factor of BST in the sintering procedure. Additionally, both Scanning Electron Microscope (SEM) and X-ray diffraction (XRD) analysis showed that the grain size of Ce-doped BST was dependent on the Ce content. Further more, the dielectric constant and dielectric loss had a curve relationship with increasing Ce content. The improvement of the electrical properties of Ce doping BST may be related to the decrease in the concentration of oxygen vacancies. According to the research, the diameter of grain, the dielectric constant and loss factor of the 1mol% Ce-doped Ba0.2Sr0.8TiO3 were 500nm, 365.8 and 0.0063, respectively.

Preparation of LiFePO4/C Composite Powders

2011 ◽  
Vol 391-392 ◽  
pp. 377-380
Author(s):  
Guo Jun Li ◽  
Ming Yang ◽  
Hai Li Jing ◽  
Rui Ming Ren
Keyword(s):  
Citric Acid ◽  
Oxalic Acid ◽  
Specific Capacity ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
Composite Powders ◽  
Charge Capacity ◽  
X Ray ◽  
Initial Charge

LiFePO4/C composite powders were prepared by a simple reaction of as-synthesized FePO4•2H2O, LiOH•H2O, oxalic acid and citric acid. The influence of oxalic acid and citric acid in different ratios was investigated on morphology and electrochemical performance of LiFePO4/C composite powders. The characterization of the composites included X-ray diffraction (XRD) and scanning electron microscopy (SEM). The XRD analysis indicates that the material is well crystallized without impurities. The obtained LiFePO4/C composite powders with well dispersion at CA/OA ratio of 1:1.50 and the initial charge capacity reached 159.3 mAhg-1 at 0.1C rate, meanwhile, the particles prepared at 1:0.75 were close to spherical in shape and the specific capacity value was 149.8 mAhg-1 at 0.1C rate, with a slight decrease on greater C-rates reaching 141.3 mAhg-1 at 1C.

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