scholarly journals Coal bottom ash characterization aiming the incorporation in cellular concrete

2021 ◽  
Vol 26 (3) ◽  
Author(s):  
Fernanda Pacheco ◽  
Michael Anderson Bica Moreira ◽  
Marlova Piva Kuwakowiski ◽  
Feliciane Andrade Breh ◽  
Bernardo Fonseca Tutikian
Keyword(s):  
Silica Fume ◽  
Bottom Ash ◽  
Spherical Shape ◽  
High Rate ◽  
Strength Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Coal Bottom Ash ◽  
The Impact ◽  
Cellular Concrete

ABSTRACT Ahead of the incorporation of residues in concrete composition, there is a decline in the environmental impact of buildings. One of the goals of today’s development is the employment of low-impact energy sources, such as thermoelectric. Thermoelectric industries display a high rate of residues, among which is pointed out coal bottom ash (CBA) (15% total residues), which have density superior to fly ash and accumulates in silos. Considering this scenario, this paper assessed the incorporation feasibility of CBA in the composition of cellular concrete, replacing silica fume. This study comprehended CBA characterization and application. For such, it was performed a scanning electron microscope (SEM) associated with Energy dispersive spectroscopy (EDS) analysis, laser granulometry, X-ray diffraction (XRD), X-ray efflorescence and density. Following the incorporation of the residues in cellular concrete in place of silica fume, it was performed compression strength analysis and SEM anew, evaluating the impact of CBA’s insertion in concrete’s microstructure. The XRD results are complementary to the other analyses. With SEM technique, it was observed the predominance of spherical-shape particles. The compressive strength of CBA concretes was superior to the reference concrete from 0,13 to 0,74MPa.

Effect of Seed Amounts on the Synthesis of Zeolite ZSM-5 Using Coal Bottom Ash and Rice Husk as Sources of Silica and Alumina by Using Seeding Method

2019 ◽  
Vol 948 ◽  
pp. 9-13
Author(s):  
Anggun Lestari ◽  
Simparmin B. Ginting ◽  
Hens Saputra
Keyword(s):  
Rice Husk ◽  
Bottom Ash ◽  
Molar Ratio ◽  
Organic Template ◽  
X Ray Diffraction ◽  
X Ray ◽  
Coal Bottom Ash ◽  
Seeding Method ◽  
Percent Crystallinity ◽  
Scanning Electron

ZSM-5 has been successfully synthesized by seeding method using coal bottom ash and rice husk as the sources of silica and alumina.Synthesis ZSM-5 were performed by the hydrothermal method in autoclave autogenous at 180 °C for 36 h with molar ratio 10Na : 50SiO : 2Al2O3 : 500H2O with the addition of ZSM-5 commercial as seed. In this experiments, investigated variations seed amounts of 5, 10, 15, and 20% of weight silica. The product was characterized using X-Ray Diffraction (XRD), Fourier Transform Infrared (FTIR), Scanning Electron Microscope (SEM), and Brunauer-Emmet-Teller (BET). Resulted showed that ZSM-5 succeed formed in all variation of seed contain. At variation seed amount 5%, crystallinity obtained still low in which content of quartz phase still be high. Percent crystallinity highest obtained at the variation of seed amount 20% with the result percent crystallinity relative 106%. The experimental results revealed that phase transformation has occurred, in which an amorphous phase of coal bottom ash and rice husk has been transformed to the ZSM-5 crystal with addition seed as substitution organic template.

scholarly journals The impact of point defects in n-type GaN layers on thermal decomposition of InGaN/GaN QWs

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Mikolaj Grabowski ◽  
Ewa Grzanka ◽  
Szymon Grzanka ◽  
Artur Lachowski ◽  
Julita Smalc-Koziorowska ◽  
...  
Keyword(s):  
Quantum Wells ◽  
High Temperatures ◽  
Point Defects ◽  
X Ray Diffraction ◽  
Helium Ions ◽  
X Ray ◽  
Sapphire Substrates ◽  
Transmission Electron ◽  
The Impact ◽  
Ingan Quantum Wells

AbstractThe aim of this paper is to give an experimental evidence that point defects (most probably gallium vacancies) induce decomposition of InGaN quantum wells (QWs) at high temperatures. In the experiment performed, we implanted GaN:Si/sapphire substrates with helium ions in order to introduce a high density of point defects. Then, we grew InGaN QWs on such substrates at temperature of 730 °C, what caused elimination of most (but not all) of the implantation-induced point defects expanding the crystal lattice. The InGaN QWs were almost identical to those grown on unimplanted GaN substrates. In the next step of the experiment, we annealed samples grown on unimplanted and implanted GaN at temperatures of 900 °C, 920 °C and 940 °C for half an hour. The samples were examined using Photoluminescence, X-ray Diffraction and Transmission Electron Microscopy. We found out that the decomposition of InGaN QWs started at lower temperatures for the samples grown on the implanted GaN substrates what provides a strong experimental support that point defects play important role in InGaN decomposition at high temperatures.

scholarly journals X-Ray Diffraction Analysis of Bottom Ash Waste after Plasma Treatment

2017 ◽  
Vol 189 ◽  
pp. 012021
Author(s):  
G Volokitin ◽  
Yu Abzaev ◽  
N Skripnikova ◽  
O Volokitin ◽  
V Shekhovtsov
Keyword(s):  
Diffraction Analysis ◽  
Plasma Treatment ◽  
Bottom Ash ◽  
X Ray Diffraction ◽  
X Ray

scholarly journals Investigation and Modeling of the Electrical Conductivity of Graphene Nanoplatelets-Loaded Doped-Polypyrrole

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1034
Author(s):  
Oladipo Folorunso ◽  
Yskandar Hamam ◽  
Rotimi Sadiku ◽  
Suprakas Sinha Ray ◽  
Neeraj Kumar
Keyword(s):  
Electrical Conductivity ◽  
Structural Changes ◽  
Spherical Shape ◽  
Graphene Nanoplatelets ◽  
Conductivity Measurements ◽  
X Ray Diffraction ◽  
X Ray ◽  
Thermogravimetric Analyzer ◽  
Energy Storage Applications ◽  
Electrical Conductivity Data

In this study, a hybrid of graphene nanoplatelets with a polypyrrole having 20 wt.% loading of carbon-black (HGPPy.CB20%), has been fabricated. The thermal stability, structural changes, morphology, and the electrical conductivity of the hybrids were investigated using thermogravimetric analyzer, differential scanning calorimeter, X-ray diffraction analyzer, scanning electron microscope, and laboratory electrical conductivity device. The morphology of the hybrid shows well dispersion of graphene nanoplatelets on the surface of the PPy.CB20% and the transformation of the gravel-like PPy.CB20% shape to compact spherical shape. Moreover, the hybrid’s electrical conductivity measurements showed percolation threshold at 0.15 wt.% of the graphene nanoplatelets content and the curve is non-linear. The electrical conductivity data were analyzed by comparing different existing models (Weber, Clingerman and Taherian). The results show that Taherian and Clingerman models, which consider the aspect ratio, roundness, wettability, filler electrical conductivity, surface interaction, and volume fractions, closely described the experimental data. From these results, it is evident that Taherian and Clingerman models can be modified for better prediction of the hybrids electrical conductivity measurements. In addition, this study shows that graphene nanoplatelets are essential and have a significant influence on the modification of PPy.CB20% for energy storage applications.

Ionic conductivity in nanocrystalline Gd doped ceria

2008 ◽  
Vol 1122 ◽  
Author(s):  
Gianguido Baldinozzi ◽  
David Simeone ◽  
Dominique Gosset ◽  
Mickael Dollé ◽  
Georgette Petot-Ervas
Keyword(s):  
Grain Size ◽  
Ionic Conductivity ◽  
Sol Gel ◽  
Doped Ceria ◽  
Narrow Size Distribution ◽  
Conductivity Measurements ◽  
X Ray Diffraction ◽  
X Ray ◽  
Grain Sizes ◽  
The Impact

AbstractWe have synthesized Gd-doped ceria polycrystalline samples (5, 10, 15 %mol), having relative densities exceeding 95% and grain sizes between 30 and 160 nm after axial hot pressing (750 °C, 250 MPa). The samples were prepared by sintering nanopowders obtained by sol-gel chemistry methods having a very narrow size distribution centered at about 16 nm. SEM and X-ray diffraction were performed to characterize the sample microstructures and to assess their structures. We report ionic conductivity measurements using impedance spectroscopy. It is important to investigate the properties of these systems with sub-micrometric grains and as a function of their composition. Therefore, samples having micrometric and nanometric grain sizes (and different Gd content) were studied. Evidence of Gd segregation near the grain boundaries is given and the impact on the ionic conductivity, as a function of the grain size and Gd composition, is discussed and compared to microcrystalline samples.

scholarly journals Lanthanoid Complexes Supported by Retro-Claisen Condensation Products of β-Triketonates

2018 ◽  
Author(s):  
Laura Abad Galán ◽  
Alexandre N. Sobolev ◽  
Eli Zysman-Colman ◽  
Mark Ogden ◽  
Massimiliano Massi
Keyword(s):  
Chelating Ligands ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
Claisen Condensation ◽  
X Ray ◽  
Condensation Products ◽  
Complexation Reactions ◽  
The Impact ◽  
Low Solubility

<i>β</i>-Triketonates have been recently used as chelating ligands for lanthanoid ions, presenting unique structures varying from polynuclear assemblies to polymers. In an effort to overcome low solubility of the complexes of tribenzoylmethane, four <i>β</i>-triketones with higher lipophilicity were synthesised. Complexation reactions were performed for each of these molecules using different alkaline bases in alcoholic media. X-ray diffraction studies suggested that the ligands were undergoing decomposition under the reaction conditions. This is proposed to be caused by <i>in situ</i>retro-Claisen condensation reactions, consistent with two examples that have been reported previously. The lability of the lanthanoid cations in the presence of a varying set of potential ligands gave rise to structures where one, two, or three of the molecules involved in the retro-Claisen condensationreaction were linked to the lanthanoid centres. These results, along with measurements of ligand decomposition in the presence of base alone, suggest that using solvents of lower polarity will mimimise the impact of the retro-Claisen condensation in these complexes. <br>

scholarly journals Influence of the Para-Substituent in Lanthanoid Complexes of Bistetrazole Substituted Calix[4]arenes

2019 ◽  
Author(s):  
Rene Z.H. Phe ◽  
Brian Skelton ◽  
Massimiliano Massi ◽  
Mark Ogden
Keyword(s):  
Structural Changes ◽  
Cluster Formation ◽  
Ammonium Cation ◽  
Ammonium Salts ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray ◽  
Mononuclear Complexes ◽  
Scattering Measurements ◽  
The Impact

5,11,17,23-Tetra-tert-butyl-25,27-dihydroxy-26,28-bis(tetrazole-5-ylmethoxy)calix[4]arene has been reported to form remarkable Ln19 and Ln12 elongated clusters, upon addition of aqueous ammonium carboxylates. The impact of the <i>para</i> substituent on lanthanoid cluster formation has been studied by synthesising two new bis-tetrazole calixarenes, with <i>p</i>-H, and <i>p</i>-allyl substituents. Solution phase dynamic light scattering measurements of the reaction mixtures indicated that clusters are not formed with the <i>p</i>-H and <i>p</i>-allyl derivatives, in contrast with the behaviour of the <i>t-</i>butyl analogue. Lanthanoid complexes of the <i>p</i>-H and <i>p</i>-allyl calixarenes were characterised by single crystal X-ray diffraction, and were found to form mononuclear complexes, linked to form a one-dimensional coordination polymer for the <i>p</i>-allyl system. All of the complexes were isolated as ammonium salts, with ammonium cation included in the calixarene cavity in most cases. It is concluded that the nature of the <i>para</i> substituent has a profound impact on the lanthanoid cluster formation process, and derivatives with more subtle structural changes will be required to determine if additional lanthanoid “bottlebrush” clusters can be isolated.<br><br>

Experimental Investigation on Intensity and Residual Stress in Superficial Layers Induced by Water Cavitation Peening with Aeration

2008 ◽  
Vol 373-374 ◽  
pp. 754-757 ◽  
Author(s):  
Dong Ying Ju ◽  
B. Han
Keyword(s):  
Residual Stress ◽  
Process Capability ◽  
Diffraction Method ◽  
Spring Steel ◽  
Bubble Collapse ◽  
Process Conditions ◽  
X Ray Diffraction ◽  
X Ray ◽  
Enhancement Method ◽  
The Impact

Water cavitation peening (WCP) with aeration is a novel surface enhancement method. A new ventilation nozzle with aeration is adopted to improve the process capability of WCP by increasing the impact pressure induced by the bubble collapse on the surface of components. In this study, in order to investigate the process capability of the WCP with aeration, a standard N-type almen strips of spring steel SAE 1070 was treated by WCP with various process conditions, and the arc height value and the residual stress in the superficial layers were measured by X-ray diffraction method. The optimal fluxes of aeration and the optimal standoff distances were achieved.

Fabrication and Microstructure of Ge-Sb-S-CsCl Chalcogenide Glass Containing β-GeS2 Nanocrystals

2014 ◽  
Vol 665 ◽  
pp. 119-123
Author(s):  
Ji Yan Hao ◽  
Hai Tao Liu
Keyword(s):  
Chalcogenide Glass ◽  
Spherical Shape ◽  
Orthorhombic Phase ◽  
Far Infrared ◽  
X Ray Diffraction ◽  
Base Glass ◽  
X Ray ◽  
Transmission Electron ◽  
Infrared Spectral ◽  
Quenching Method

we report the fabrication and microstructure of Ge-Sb-S-CsCl chalcogenide glass containing β-GeS2 nanocrystals. A Ge-Sb-S-CsCl chalcogenide base glass with the better crystalline ability is first fabricated by melt-quenching method, and a further careful thermal process has led to the formation of β-GeS2 nanocrystals in the glass. Transmission electron microscopy showed that the size of β-GeS2 nanocrystals with nearly monodisperse spherical shape ranges from 30 to 45 nm in the glass. Powder X-ray diffraction results confirm that the β-GeS2 nanocrystals are of high crystallization with orthorhombic phase. Energy dispersive spectroscopy is employed for the information of nanocrystals glass composition. It is worthwhile to note that the obtained Ge-Sb-S-CsCl chalcogenide glass containing β-GeS2 nanocrystals still keeps higher transmittance in mid- and far- infrared spectral region.

scholarly journals A novel technique to synthesis of tenorite (CuO) nanoparticles from low concentration CuSO4 solution

2011 ◽  
Vol 47 (1) ◽  
pp. 73-78 ◽  
Author(s):  
E. Darezereshki ◽  
F. Bakhtiari
Keyword(s):  
Electron Microscopy ◽  
Decomposition Method ◽  
Raw Materials ◽  
Spherical Shape ◽  
Cuo Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Thermal Decomposition Method ◽  
Novel Technique ◽  
Transmission Electron

In this study CuO nanoparticles were prepared via direct thermal decomposition method using basic copper sulphates as wet chemically synthesized precursor which was calcined in air at 750?C for 2h. Samples were characterized by thermogravimetric (TG-DSC), X-ray diffraction (XRD), energy dispersive spectroscopy (EDS), infrared spectrum (IR), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The XRD, EDS, and IR results indicated that the synthesized CuO particles were pure. The SEM and TEM results showed that the CuO nanoparticles were of approximate spherical shape, and 170?5 nm in size. Using this method, Cuo nanoparticles could be produced without using organic solvent, expensive raw materials, and complicated equipment.

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