scholarly journals Extraction of γ-Alumina from Low-Cost Kaolin

Resources ◽  
2018 ◽  
Vol 7 (4) ◽  
pp. 63
Author(s):  
Khalil Ibrahim ◽  
Mohammad Moumani ◽  
Salsabeela Mohammad
Keyword(s):  
Low Cost ◽  
Morphological Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Aluminum Metal ◽  
Alumina Particles ◽  
Two Stages ◽  
Method Of Extraction ◽  
Microcrystalline Powder ◽  
Made In

A combined process is proposed for the utilization of local kaolin to produce alumina particles. The applied process is made in two stages: calcination at 700 °C with sodium chloride and leaching with sulfuric followed by hydrochloric acids. The optimal extraction efficiency can be obtained when the conditions are as follows: leaching temperature is at 140 °C, leaching time is 3 h 45 min and concentration of sulfuric acid is 40 wt.%. The results show that the purity of alumina reaches 79.28%, which is suitable for the production of aluminum metal. It is evident that this method of extraction of alumina from the kaolin ash is practical and feasible. The structural and morphological properties of the calcined microcrystalline powder was characterized by X-ray diffraction and scanning electron microscope (SEM).

Fast growth of pure V2O5 nanoparticles by low-cost hydrothermal process

2021 ◽  
Vol 96 (3) ◽  
pp. 30101
Author(s):  
Fariza Ferhati ◽  
Aline Simo ◽  
Mohammed S. Belkaid ◽  
Malek Maaza ◽  
Ouiza Boussoum ◽  
...  
Keyword(s):  
Low Cost ◽  
Hydrothermal Process ◽  
Orthorhombic Phase ◽  
Growth Conditions ◽  
Time Dependent ◽  
Morphological Properties ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray ◽  
Transmission Electron

Vanadium pentoxide (V2O5) nanorods were successfully grown through an easy, quick and clean hydrothermal method using vanadium oxide sols (V2O5.1,6H2O) as precursor. Structurals studies based on the X-ray diffraction and Raman spectroscopy revealed that the synthesized nanomaterials are pure divanadium pentoxide with an orthorhombic phase. The morphological properties and the particle size of the developed V2O5 nanoparticles were investigated by scanning electron microscopy (SEM) and high resolution transmission electron microscope (HRTEM). The results show that the as-grown samples consist of a large amount of one-dimensional V2O5 nanorods with the widths approximately 52 nm and the lengths are up to several hundred nanometers. The effects of different growth conditions, such as hydrothermal duration and stirring temperature of the precursor on the formation of the nanorods has been recorded. Moreover, the structural and morphological properties of the resulting nanopowders have been experimentally studied. Time-dependent experiments showed that V2O5.1,6H2O were dehydrated progressively and transformed into orthorhombic V2O5 single-crystalline nanorods. It has been established that high stirring temperature of the precursor is benefical for the formation of V2O5 nanorods and minimizes the duration time of the heat treatment. Hence the adjusted parameters (time and temperature) appears to be the key element to achieving the desired nanomaterial with defined forms.

scholarly journals Multidimensional Ln-Aminophthalate Photoluminescent Coordination Polymers

Materials ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1786
Author(s):  
Carla Queirós ◽  
Chen Sun ◽  
Ana M. G. Silva ◽  
Baltazar de Castro ◽  
Juan Cabanillas-Gonzalez ◽  
...  
Keyword(s):  
Water Content ◽  
Coordination Polymers ◽  
Metal Ion ◽  
Low Cost ◽  
Microwave Assisted Synthesis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Wide Range ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

The development of straightforward reproducible methods for the preparation of new photoluminescent coordination polymers (CPs) is an important goal in luminescence and chemical sensing fields. Isophthalic acid derivatives have been reported for a wide range of applications, and in addition to their relatively low cost, have encouraged its use in the preparation of novel lanthanide-based coordination polymers (LnCPs). Considering that the photoluminescent properties of these CPs are highly dependent on the existence of water molecules in the crystal structure, our research efforts are now focused on the preparation of CP with the lowest water content possible, while considering a green chemistry approach. One- and two-dimensional (1D and 2D) LnCPs were prepared from 5-aminoisophthalic acid and Sm3+/Tb3+ using hydrothermal and/or microwave-assisted synthesis. The unprecedented LnCPs were characterized by single-crystal X-ray diffraction (SCRXD), powder X-ray diffraction (PXRD), Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM), and their photoluminescence (PL) properties were studied in the solid state, at room temperature, using the CPs as powders and encapsulated in poly(methyl methacrylate (PMMA) films, envisaging the potential preparation of devices for sensing. The materials revealed interesting PL properties that depend on the dimensionality, metal ion, co-ligand used and water content.

Plastic deformations in kyanites by tectonometamorphic processes: a single-crystal X-ray diffraction study

2009 ◽  
Vol 73 (3) ◽  
pp. 359-371 ◽  
Author(s):  
G. D. Gatta ◽  
N. Rotiroti ◽  
M. Zucali
Keyword(s):  
Single Crystal ◽  
X Ray Diffraction ◽  
Plastic Deformations ◽  
X Ray ◽  
Deformational History ◽  
Significant Difference ◽  
Elliptical Section ◽  
History Of ◽  
Diffraction Patterns ◽  
Two Stages

AbstractThe crystalch emistry and crystal structure of naturalky anite crystals from the Eclogitic Micaschists Complex of the Sesia-Lanzo Zone, Western Italian Alps, have been investigated by means of optical microscopy, wavelength dispersive X-ray microanalysis, and single-crystal X-ray diffraction. The association of kyanite + garnet + phengitic-mica + chloritoid suggests that the eclogite-facies stages occurred at P ≤ 2.1 GPa and T ≤ 650ºC. Kyanite grains are large (cm-sized) porphyroblasts grown dynamically during one of the deformational events related to the subduction of the Austroalpine continentalcr ust. Under the polarizing microscope, kyanite grains show almost homogeneous cores, whereas rims are sometimes symplectitic aggregates of quartz and kyanite, confirming at least two stages of growth most likely related to the multistage deformational history of these rocks. Chemical analysis shows that Fe3+ is the major substituting cation for Al3+, ranging between 0.038 and 0.067 a.p.f.u.The single-crystal X-ray diffraction investigation of the kyanites shows severely textured patterns on the (h0l)*-plane. Such evidence is not observed in the unwarped diffraction patterns on (0kl)* and (hk0)*. The most significant difference between the structuralp arameters refined in this study, with respect to those of previously published unstrained gem-quality crystals, concerns the displacement parameters. The anisotropic displacement ellipsoids of all the atomic sites are significantly larger than those previously described, and systematically oriented with the largest elliptical section almost perpendicular to [010]. The larger ellipsoids in the kyanite crystal investigated here reflect the displacement of the centre of gravity of the electron distribution, rather than an anomalous atomic thermal motion. The magnitude and orientation of the displacement parameters and the textured/strained diffraction pattern may be the result of two combined effects: (1) that the kyanite crystals are actually composed of several blocks; (2) the crystals are affected by a pervasive residual strain, as a result of tectonometamorphic plastic deformations and re-crystallization.

Growth mechanism and characterization of ZnO nano-tubes synthesized using the hydrothermal-etching method

2009 ◽  
Vol 63 (6) ◽  
Author(s):  
Yan Li ◽  
Chuan-Sheng Liu ◽  
Yun-Ling Zou
Keyword(s):  
Room Temperature ◽  
Morphological Analysis ◽  
Diffraction Field ◽  
X Ray Diffraction ◽  
X Ray ◽  
Room Temperature Photoluminescence ◽  
Etching Method ◽  
Nano Rods ◽  
Two Stages

AbstractZnO nano-tubes (ZNTs) have been successfully synthesized via a simple hydrothermal-etching method, and characterized by X-ray diffraction, field emission scanning electron microscopy and room temperature photoluminescence measurement. The as-synthesized ZNTs have a diameter of 500 nm, wall thickness of 20–30 nm, and length of 5 µm. Intensity of the plane (0002) diffraction peak, compared with that of plane (10$$ \bar 1 $$0) of ZNTs, is obviously lower than that of ZnO nano-rods. This phenomenon can be caused by the smaller cross section of plane (0002) of the nano-tubes compared with that of other morphologies. On basis of the morphological analysis, the formation process of nano-tubes can be proposed in two stages: hydrothermal growth and reaction etching process.

A simple and low-cost solution for the automation of X-ray powder diffractometers with chart recorder output

2006 ◽  
Vol 39 (4) ◽  
pp. 626-629
Author(s):  
M. Jayaprakasan ◽  
V. Kannan ◽  
P. Ramasamy
Keyword(s):  
Quantitative Analysis ◽  
Low Cost ◽  
Hard Copy ◽  
X Ray Diffraction ◽  
Raw Data ◽  
Crystalline Materials ◽  
X Ray ◽  
Strip Chart ◽  
Controlled Systems ◽  
Chart Recorder

X-ray powder diffraction is an established method for the qualitative identification of crystalline materials and their quantitative analysis. The new generation of X-ray diffraction systems are based on expensive digital/embedded control technology and computer interfaces. Yet many laboratories use conventional manual-controlled systems withXYstrip-chart recorders. Since the output spectrum is a strip chart (hard copy), raw data, essential for structural and qualitative analysis, are not readily available for further analysis. Upgrading to modern computerized diffractometers is very expensive. The proposed automation design described here is intended to enable the conventional diffractometer user to collect, store and analyze data quickly. The design also improves the resolution by five times compared with the conventional setup. For the automation, a PC add-on card has been designed to control and collect the timing and intensity counts from the conventional X-ray diffractometer, and suitable software has been developed to collect, process and present the X-ray diffraction data for both qualitative and quantitative analysis. Moreover, a major advantage of this design is that it does not warrant any physical modification of the hardware of the conventional setup; it is simply an extension to enhance the performance of collecting raw data with a higher resolution at desired intervals/timings.

Synthesis of Silica Modified Large-Sized Hydroxyapatite Whiskers by a Hydrothermal Co-Precipitation Method

2015 ◽  
Vol 645-646 ◽  
pp. 1339-1344 ◽  
Author(s):  
Yan Ting Yin ◽  
Qing Hua Chen ◽  
Ting Ting Yan ◽  
Qing Hua Chen
Keyword(s):  
Bone Repair ◽  
Ethanol Solution ◽  
Morphological Properties ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
New Type ◽  
Ft Ir ◽  
Co Precipitation ◽  
Surface Modified

The objective of this study was to develop a novel silica modified large-sized hydroxyapatite whiskers with improved properties for use in bone repair applications. Large-sized whiskers with a mean length of 250μm were obtained by a hydrothermal co-precipitation method at 150°C, 7.5Mpa in high-pressure reactor. Silica modified hydroxyapatite whiskers were prepared by dissolving TEOS in ethanol solution, then sintering with hydroxyapatite. The compositional and morphological properties of prepared whiskers were studied by means of x-ray diffraction (XRD), Fouier transform infrared (FT-IR), scanning electron microscopy (SEM). The results indicated the evidence of nanosilicon dioxide particles on the surface of HAP whiskers. The size of nanosilicon dioxide particles depends on dropping and stirring rate. Hence, this new type of silica modified large-sized hydroxyapatite whiskers is a valuable candidate for biomedical applications.Key words: hydroxyapatite, hydrothermal co-precipitation, surface modified, whiskers

Assessment of Laser Effects on the Structure and Electrical Properties of the Compound Bi2-xAgxSr2Ca2Cu3O10+δ Superconducting

2021 ◽  
Vol 19 (11) ◽  
pp. 108-115
Author(s):  
Nihad Ali Shafeek
Keyword(s):  
Critical Temperature ◽  
Hydraulic Press ◽  
Electrical Characteristics ◽  
X Ray Diffraction ◽  
Solid State Method ◽  
X Ray ◽  
Compensation Ratio ◽  
Superconducting Compound ◽  
State Method ◽  
Two Stages

This research contains preparing the superconducting compound Bi2-xAgxSr2Ca2Cu3O10+δ and studying its structural and electrical characteristics. The samples were prepared using the solid-state method in two stages, and different concentrations of x were (x= 0.2,0.4,0.6,0.8) replaced instead of bismuth Bi. Then, using a hydraulic press 9 ton/cm2 and sintering with a temperature of 850°C, the samples were pressed. Next, x-ray diffraction is used to study the structural properties. The study of these samples was presented in different proportions of x values, where x = 0.4 is the best compensation ratio of x. A critical temperature of 1400C and the Tetragonal structure was got. After that, the effect of laser nidinium _ yak (Nd: YAG laser) was used on the compositional. It was found that the temperature value increased, so we got the best critical temperature, which is 142 0C.

Low-cost thermo-chemical process of TiO2 powder purification: Study of iterative gettering effect

2021 ◽  
Author(s):  
Nesrine Jaouabi ◽  
Wala Medfai ◽  
Marouan Khalifa ◽  
Rabia Zaghouani ◽  
Hatem Ezzaouia
Keyword(s):  
Porous Layer ◽  
Sacrificial Layer ◽  
Low Cost ◽  
Nir Spectroscopy ◽  
Tio2 Powder ◽  
X Ray Diffraction ◽  
X Ray ◽  
Density Reduction ◽  
Transmission Electron ◽  
Layer Effect

The titanium dioxide (TiO2) purity is very important for the TiO2-based applications making essential the impurities density reduction. In this study, we propose an efficient purification process of TiO2 powder in order to reduce impurities. The low-cost proposed approach is based on an iterative gettering (IG) process combining three main steps: (1) a porous TiO2 sacrificial layer formation (p-TiO2), (2) a rapid thermal annealing (RTA) of p-TiO2 powder in an infrared oven at 950°C under air permitting the residual impurities diffusion to the porous layer surface and (3) etching in acid solution to remove the porous layer. Effect of the proposed gettering process on purification efficiency was evaluated by different characterization techniques such as the transmission electron microscopy (TEM), the energy dispersive x-ray spectroscopy (EDX), the UV–Visible-NIR spectroscopy, the X-ray diffraction (XRD) and atomic absorption spectroscopy (AAS). The obtained results showed the efficient removal of metal impurities, such as Cu, Al, P, and Fe confirming the efficiency of the process improving the purity from 89% to 99.96%.

scholarly journals STARCH MEDIATED SYNTHESIS OF HYDROXYAPATITE NANOPARTICLE FOR BIOMEDICAL APPLICATIONS

2015 ◽  
Vol 2 (1) ◽  
pp. 15-17
Author(s):  
Indira J
Keyword(s):  
Biomedical Applications ◽  
Soluble Starch ◽  
Morphological Properties ◽  
Spherical Nanoparticles ◽  
Hydroxyapatite Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Average Size ◽  
Controllable Size

Hydroxyapatite (HAP) nanoparticles with uniform morphologies and controllable size have been synthesized by template directed method. The environment and eco-friendly polysaccharide soluble starch is used as a template to regulate size and shape of the nanoparticles synthesized. Structural and morphological properties of as-synthesized hydroxyapatite nanoparticles have been examined through the techniques like Fourier Transform Infrared Spectroscopy (FT-IR), X-ray Diffraction (XRD) and Scanning Electron Microscopy(SEM), respectively. The results indicate that the obtained particles are uniform discrete spherical nanoparticles. The average size of the hydroxyapatite nanoparticles were ranged from 45 to 60 nm.

scholarly journals Fast X-Ray Diffraction (XRD) Tomography for Enhanced Identification of Materials

2021 ◽  
Author(s):  
Airidas Korolkovas ◽  
Alexander Katsevich ◽  
Michael Frenkel ◽  
William Thompson ◽  
Edward Morton
Keyword(s):  
Graphics Processing Unit ◽  
Low Cost ◽  
Photon Counting ◽  
Finite Size ◽  
Processing Unit ◽  
X Ray Diffraction ◽  
X Ray ◽  
Specific Material ◽  
Xrd Patterns ◽  
Graphics Processing

X-ray computed tomography (CT) can provide 3D images of density, and possibly the atomic number, for large objects like passenger luggage. This information, while generally very useful, is often insufficient to identify threats like explosives and narcotics, which can have a similar average composition as benign everyday materials such as plastics, glass, light metals, etc. A much more specific material signature can be measured with X-ray diffraction (XRD). Unfortunately, XRD signal is very faint compared to the transmitted one, and also challenging to reconstruct for objects larger than a small laboratory sample. In this article we analyze a novel low-cost scanner design which captures CT and XRD signals simultaneously, and uses the least possible collimation to maximize the flux. To simulate a realistic instrument, we derive a formula for the resolution of any diffraction pathway, taking into account the polychromatic spectrum, and the finite size of the source, detector, and each voxel. We then show how to reconstruct XRD patterns from a large phantom with multiple diffracting objects. Our approach includes a reasonable amount of photon counting noise (Poisson statistics), as well as measurement bias, in particular incoherent Compton scattering. The resolution of our reconstruction is sufficient to provide significantly more information than standard CT, thus increasing the accuracy of threat detection. Our theoretical model is implemented in GPU (Graphics Processing Unit) accelerated software which can be used to assess and further optimize scanner designs for specific applications in security, healthcare, and manufacturing quality control.

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