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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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Spratt, Henry
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (5/5 displayed)
- 2017A comparative study of electrochemical, optical properties and electropolymerization behavior of thiophene- and furan-substituted diketopyrrolopyrrolecitations
- 2016Investigation of the electrochemical growth of a Cu-Zn-Sn film on a molybdenum substrate using a citrate solutioncitations
- 2014Location of hydrogen atoms in hydronium jarositecitations
- 2009Thermal decomposition of hydrotalcites with variable cationic ratioscitations
- 2008Thermal decomposition of synthesized layered double hydroxides based upon Mg/(Fe,Cr) and carbonatecitations
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article
Thermal decomposition of hydrotalcites with variable cationic ratios
Abstract
Thermal analysis complimented with evolved gas mass spectrometry has been applied to hydrotalcites containing carbonate prepared by coprecipitation and with varying divalent-trivalent cation ratio. The resulting materials were characterized by XRD, and TGA/DTG to determine the stability of the hydrotalcites synthesised. Hydrotalcites of formula Mg4(Fe,Al)2(OH)16(CO3,Cl).4H2O, Mg6(Fe,Al)2(OH)16(CO3,Cl).4H2O, and Mg8(Fe,Al)2(OH)16(CO3,Cl).4H2Oformed by intercalation with the carbonate anion as a function of divalent/trivalent cationic ratio show variation in the d-spacing attributed to the size of the cation. The thermal decomposition of carbonate hydrotalcites consist of two decomposition steps between 300 and 400 ˚C, attributed to the simultaneous dehydroxylation and decarbonation of the hydrotalcite lattice. Water loss ascribed to dehydroxylation occurs in two decomposition steps, where the first step is due to the partial dehydroxylation of the lattice, while the second step is due to the loss of water interacting with the interlayer anions. Dehydroxylation results in the collapse of the hydrotalcite structure to that of its corresponding metal oxides, including MgO, MgAl2O4, and MgFeAlO4.