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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Bell, Anthony Martin Thomas
Sheffield Hallam University
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (14/14 displayed)
- 2024Atom Probe Tomography Investigation of Clustering in Model P2O5-Doped Borosilicate Glasses for Nuclear Waste Vitrification
- 2023Dynamic high‐temperature crystallization and processing properties of industrial soda–lime–silica glassescitations
- 2021Thermostructural and Elastic Properties of PbTe and Pb0.884Cd0.116Te: A Combined Low-Temperature and High-Pressure X-ray Diffraction Study of Cd-Substitution Effectscitations
- 2021Crystal structures and X-ray powder diffraction data for Cs2NiSi5O12, RbGaSi2O6, and CsGaSi2O6 synthetic leucite analogues
- 2020X-ray Fluorescence Analysis of Feldspars and Silicate Glass: Effects of Melting Time on Fused Bead Consistency and Volatilisationcitations
- 2016Rietveld refinement of the crystal structures of Rb2XSi5O12(X= Ni, Mn)citations
- 2013Synchrotron X-ray powder diffraction study on synthetic Sr-Fresnoitecitations
- 2012High-temperature synchrotron X-ray powder diffraction study of Cs2XSi5O12(X = Cd, Cu, Zn) leucitescitations
- 2010Revision of the structure of Cs2CuSi5O12 leucite as orthorhombic Pbcacitations
- 2010Structural evolution of aqueous mercury sulphide precipitates: energy-dispersive X-ray diffraction studiescitations
- 2009Crystal structures and cation ordering in Cs2MgSi5O12, Rb2MgSi5O12 and Cs2ZnSi5O12 leucitescitations
- 2009Synchrotron X-ray absorption spectroscopy and X-ray powder diffraction studies of the structure of johnbaumite [Ca10(AsO4)6(OH,F)2] and synthetic Pb-, Sr- and Ba-arsenate apatites and some comments on the crystal chemistry of the apatite structure type in generalcitations
- 2008Polymorphism in cyclohexanolcitations
- 2001Chemically induced magnetism and magnetoresistance in La(0.8)Sr(1.2)Mn(0.6)Rh(0.4)O(4).
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article
Dynamic high‐temperature crystallization and processing properties of industrial soda–lime–silica glasses
Abstract
<jats:title>Abstract</jats:title><jats:p>In situ dynamic crystallization properties of industrial soda–lime–silica glasses at realistic processing temperatures have not yet been explored. Hence, we collected in situ high‐temperature X‐ray diffraction patterns for 10 different industrially manufactured soda–lime–silica glasses as a function of temperature between 900 and 1200°C to investigate the phase relations in their devitrified melts. The high‐temperature X‐ray diffraction study was complemented by measuring the liquidus temperature of those glasses by the temperature gradient technique. A multiple variable regression analysis was applied to the experimental and modeled data to produce a predictive model for the rate of solidification and liquidus temperature based on glass composition. We have demonstrated that forms of quartz (SiO<jats:sub>2</jats:sub>) and Na<jats:sub>2</jats:sub>CaSiO<jats:sub>4</jats:sub>, which are not traditionally identified by room temperature X‐ray diffraction studies of commercial soda–lime–silica glasses, are the dominant crystalline phases at 800 and 900°C. Upon further heating, different forms of cristobalite become the primary phase field prior to the formation of X‐ray amorphous melts, irrespective of the glass composition. Sporadic unidentified as well as high‐temperature stable SiO<jats:sub>2</jats:sub> polymorphs that are not recoverable to room temperature were also observed. In contrast to the literature, wollastonite (CaSiO<jats:sub>3</jats:sub>) and devitrite (Na<jats:sub>2</jats:sub>Ca<jats:sub>3</jats:sub>Si<jats:sub>6</jats:sub>O<jats:sub>16</jats:sub>), which are the main predictor variables in previously developed liquidus temperature models, were not observed prior to the formation of X‐ray amorphous glass melts, and hence their influence on liquidus temperature may be questionable. It was also found that the difference between glass processing and liquidus temperatures can be excessively high, and such large temperature differences can potentially be exploited and reduced to enable decreases in melting or processing temperatures of industrial soda–lime–silica glass melts.</jats:p>