scholarly journals Waste and Solar Energy: An Eco-Friendly Way for Glass Melting

2021 ◽  
Vol 5 (2) ◽  
pp. 16
Author(s):  
Isabel Padilla ◽  
Maximina Romero ◽  
José I. Robla ◽  
Aurora López-Delgado

In this work, concentrated solar energy (CSE) was applied to an energy-intensive process such as the vitrification of waste with the aim of manufacturing glasses. Different types of waste were used as raw materials: a hazardous waste from the aluminum industry as aluminum source; two residues from the food industry (eggshell and mussel shell) and dolomite ore as calcium source; quartz sand was also employed as glass network former. The use of CSE allowed obtaining glasses in the SiO2-Al2O3-CaO system at exposure time as short as 15 min. The raw materials, their mixtures, and the resulting glasses were characterized by means of X-ray fluorescence, X-ray diffraction, and differential thermal analysis. The feasibility of combining a renewable energy, as solar energy and different waste for the manufacture of glasses, would highly contribute to circular economy and environmental sustainability.

2013 ◽  
Vol 743-744 ◽  
pp. 720-724
Author(s):  
Yong Sheng Du ◽  
Bao Wei Li ◽  
Xue Feng Zhang

Glass-ceramic in the CaO-MgO-Al2O3-SiO2 quaternary system was prepared using Baiyunebo tailing and fly ash as main raw materials by the method of melting. The processes of producing glass-ceramic included mixture, melting, molding, annealing, heat treatment, etc. The processing schedule for glass melting temperature, nucleation and crystallization temperature were chosen as 1450°C, 720°C and 850°C. The influences of glass components ratio on the structure were investigated by X-ray diffraction (XRD). It can be found that the main crystalline phase of augite, anorthite, magnesioferrite or magnetite mainly depended on glass components ratio. The results of mechanical measurements indicated that the bending strengths, density and chemical durability of glass-ceramics were concerned with the main crystal phase. The glass ceramics with augite phase had higher performance compared with others.


Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 232
Author(s):  
Pedro J. Sánchez-Soto ◽  
Eduardo Garzón ◽  
Luis Pérez-Villarejo ◽  
George N. Angelopoulos ◽  
Dolores Eliche-Quesada

In this work, an examination of mining wastes of an albite deposit in south Spain was carried out using X-ray Fluorescence (XRF), X-ray diffraction (XRD), particle size analysis, thermo-dilatometry and Differential Thermal Analysis (DTA) and Thermogravimetric (TG) analysis, followed by the determination of the main ceramic properties. The albite content in two selected samples was high (65–40 wt. %), accompanied by quartz (25–40 wt. %) and other minor minerals identified by XRD, mainly kaolinite, in agreement with the high content of silica and alumina determined by XRF. The content of Na2O was in the range 5.44–3.09 wt. %, being associated with albite. The iron content was very low (<0.75 wt. %). The kaolinite content in the waste was estimated from ~8 to 32 wt. %. The particle size analysis indicated values of 11–31 wt. % of particles <63 µm. The ceramic properties of fired samples (1000–1350 °C) showed progressive shrinkage by the thermal effect, with water absorption and open porosity almost at zero at 1200–1250 °C. At 1200 °C, the bulk density reached a maximum value of 2.38 g/cm3. An abrupt change in the phase evolution by XRD was found from 1150 to 1200 °C, with the disappearance of albite by melting in accordance with the predictions of the phase diagram SiO2-Al2O3-Na2O and the system albite-quartz. These fired materials contained as main crystalline phases quartz and mullite. Quartz was present in the raw samples and mullite was formed by decomposition of kaolinite. The observation of mullite forming needle-shape crystals was revealed by Scanning Electron Microscopy (SEM). The formation of fully densified and vitrified mullite materials by firing treatments was demonstrated.


2016 ◽  
Vol 703 ◽  
pp. 316-320
Author(s):  
Hai Feng Chen ◽  
Jing Ling Hu ◽  
Bing Xu

Using NH4VO3, Bi (NO3)3•5H2O and Co (NO3)2•6H2O as raw materials, Co doped BiVO4 (Co/BiVO4) photocatalysts were successfully prepared by solid state method. And the photo catalytic properties were test in this work. Crystal structures of these samples were characterized by X-ray diffraction (XRD). The Methyl Orange (MO) was simulated as the sewage under the visible light to explorer the influence of the illumination time and the mass of photocatalyst. The visible-light absorption spectrum of BiVO4 was broadening with doping Co. It was found that the Co/BiVO4 had higher photocatalytic activity than pure BiVO4 .The reason of enhanced catalytic effect also had been analyzed and discussed in the article.


1992 ◽  
Vol 267 ◽  
Author(s):  
Ana M De Andres ◽  
Isabel MuÑOZ

ABSTRACTNineteen roman ceramic sherds found near Salobreña (Granada, Spain), in the western coast of the Mediterranean Sea, as well as different ceramic clays from the surroundingsare studied. Both clays and ceramic sherds are characterizad by X-ray diffraction and spectrometry, differential thermal analysis, and scanning electron and optical microscopies. A good number of the ceramic pieces, among which some “Terrae Sigillatae”, have a composition similar to that of the local clays and, thus, have been probably manufactured at Salobreña. Only a few of them have a foreign origin. For most of them, the firing temperature was about 800-850 °C, although some have been produced at 900-1000 °C, and some others at 1000-1100 °C. It is concluded that Salobreña appearsto have been an important settlement just in the third century of the Christian era.


2011 ◽  
Vol 268-270 ◽  
pp. 356-359 ◽  
Author(s):  
Wen Song Lin ◽  
C. H. Wen ◽  
Liang He

Mn, Fe doped ZnO powders (Zn0.95-xMnxFe0.05O2, x≤0.05) were synthesized by an ameliorated sol-gel method, using Zn(CH3COO)2, Mn(CH3COO)2and FeCl2as the raw materials, with the addition of vitamin C as a kind of chemical reducer. The resulting powder was subsequently compacted under pressure of 10 MPa at the temperature of 873K in vacuum. The crystal structure and magnetic properties of Zn0.95-xMnxFe0.05O2powder and bulk samples have been investigated by X-ray diffraction (XRD) and vibrating sample magnetometer (VSM). X-ray photoelectron spectroscopy (XPS) was used to study chemical valence of manganese, iron and zinc in the samples. The x-ray diffraction (XRD) results showed that Zn0.95-xMnxFe0.05O (x≤0.05) samples were single phase with the ZnO-like wurtzite structure. No secondary phase was found in the XRD spectrum. X-ray photoelectron spectroscopy (XPS) showed that Fe and Mn existed in Zn0.95-xMnxFe0.05O2samples in Fe2+and Mn2+states. The results of VSM experiment proved the room temperature ferromagnetic properties (RTFP) of Mn, Fe co-doped ZnO samples.


2011 ◽  
Vol 236-238 ◽  
pp. 1712-1716 ◽  
Author(s):  
Hai Tao Liu ◽  
Jun Dai ◽  
Jia Jia Zhang ◽  
Wei Dong Xiang

Bismuth selenide (Bi2Se3) hexagonal nanosheet crystals with uniform size were successfully prepared via a solvothermal method at 160°C for 22 h using bismuth trichloride(BiCl3) and selenium powder(Se) as raw materials, sodium bisulfite(NaHSO3) as a reducing agent, diethylene glycol(DEG) as solvent, and ammonia as pH regulator. Various techniques such as X-ray diffraction (XRD), field-emission scanning electron microscope (FESEM), high-resolution transmission electron microscope (HRTEM), and selected area electron diffraction (SAED) were used to characterize the obtained products. Results show that the as-synthesized samples are pure Bi2Se3 hexagonal nanosheet crystals. A possible growth mechanism for Bi2Se3 hexagonal nanosheet crystals is also discussed based on the experiment.


2013 ◽  
Vol 787 ◽  
pp. 58-64 ◽  
Author(s):  
Xiang Feng Li ◽  
Zhao Zhang ◽  
Fang Liu ◽  
Shu Ping Zheng

The LiFePO4/C composites with different morphology are synthesized by a novel glucose assisted hydrothermal method at various glucose concentrations (from 0 to 0.25mol/L) and the insoluble lithium source Li2CO3, (NH4)2Fe (SO4)2·6H2O and (NH4)2HPO4(n (Li):n (Fe):n (P)=1:1:1) are used as raw materials. The structure, morphology, thermal performance and electrochemical properties of the synthesized composites are characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), thermogravimetry/differential scanning calorimetry (TG-DSC), galvanostatic charge/discharge tests and cyclic voltammetry (CV). The results show that the LiFePO4/C synthesized with 0.125mol/L glucose has the relatively small particles size (0.1~0.5μm) and the well spherical morphology. The optimal sample exhibits a high discharge capacity of 160.0mAh/g at the first cycle and exhibits a good reversibility and stability in CV tests.


2021 ◽  
Vol 325 ◽  
pp. 181-187
Author(s):  
Martin Nguyen ◽  
Radomír Sokolář

This article examines the influence of fly ash on corrosion resistance of refractory forsterite-spinel ceramics by molten iron as a corrosive medium. Fly ash in comparison with alumina were used as raw materials and sources of aluminium oxide for synthesis of forsterite-spinel refractory ceramics. Raw materials were milled, mixed in different ratios into two sets of mixtures and sintered at 1550°C for 2 hours. Samples were characterized by X-ray diffraction analysis and thermal dilatometric analysis. Crucibles were then made from the fired ceramic mixtures and fired together with iron at its melting point of 1535°C for 5 hours. The corrosion resistance was evaluated by scanning electron microscopy on the transition zones between iron and ceramics. Mixtures with increased amount of spinel had higher corrosion resistance and mixtures with fly ash were comparable to mixtures with alumina in terms of corrosion resistance and refractory properties.


2020 ◽  
Vol 56 (1) ◽  
pp. 1
Author(s):  
George Christidis ◽  
Katerina Paipoutlidi ◽  
Ioannis Marantos ◽  
Vasileios Perdikatsis

A great variety of fine grained industrial rocks, which are valued by the industry contain variable amounts of amorphous or poorly crystalline matter, which is not easily detectable by the conventional mineralogical analysis methods based on X-ray diffraction (XRD). The quantification of amorphous matter in industrial rocks is a major task because it provides a thorough characterization of the raw materials and assists to interpret their reactivity. Among the most reliable methods used for quantification of amorphous matter, are those which are based on Rietveld refinement. In this study we prepared 1:1 mixtures of synthetic or natural calcite and quartz with 5-80% glass flour and added corundum (α-Al2O3) internal standard and applied the Autoquan2.80 © software based on the BGMN computer code to quantify the amorphous matter content. The mixtures with synthetic minerals yielded results with minimum absolute error due to the similar particle size of the minerals, the internal standard and the glass. By contrast, the mixtures with natural minerals displayed greater relative error due to the particle size difference between the minerals on the one hand and the internal standard and the glass on the other, due to the microabsorption effect. Moreover, preferred orientation was important in the case of natural calcite, due to perfect  cleavage plane. Mixtures containing up to 25% amorphous matter did not display the characteristic hump at 20-30 °2θ, suggesting that the lack of the hump is not a safe criterion for the recognition of amorphous matter.


Cerâmica ◽  
2016 ◽  
Vol 62 (364) ◽  
pp. 386-391 ◽  
Author(s):  
J. R. M. Ferreira ◽  
L. H. L. Louro ◽  
A. M. Costa ◽  
J. B. de Campos ◽  
M. H. Prado da Silva

Abstract In the present study, hydroxyapatite and Zn-substituted hydroxyapatite powders were synthesized using ostrich eggshell as a calcium source. The samples were analyzed by scanning electron microscopy with field emission gun, and X-ray diffraction (XRD) to identify the present phases, and X-ray fluorescence spectroscopy for quantitative chemical analysis of the synthesized and heat treated powders. The Fourier transform infrared spectroscopy technique was used before and after heat treatments at 700, 900 and 1100 °C in order to identify the functional groups present, as an additional technique to the XRD analysis. The results presented in this study represent a promising method for synthesis of hydroxyapatite and hydroxyapatite partially substituted with zinc, since the results showed no undesirable phases or impurities in the produced powders. It was observed that Zn-substituted hydroxyapatite showed higher thermal stability, when compared to pure hydroxyapatite.


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