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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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Frost, Ray
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (18/18 displayed)
- 2020Volatilisation of trace elements during reduction of iron ore by hydrogencitations
- 2019Elemental deportment and chemical structure evolution of iron ore during direct reduction in hydrogen atmosphere
- 2016Environmental applications of inorganic-organic clays for recalcitrant organic pollutants removal: Bisphenol Acitations
- 2014Vibrational spectroscopy of the sulphate mineral sturmanite from Kuruman manganese deposits, South Africacitations
- 2014Infrared and raman spectroscopic characterization of the borate mineral vonsenite Fe2/2+ Fe3+BO5citations
- 2014A vibrational spectroscopic study of the phosphate mineral churchite (REE)(PO4).2H2Ocitations
- 2013Vibrational spectroscopic characterization of the phosphate mineral kulanite Ba(Fe2+,Mn2+,Mg)2(Al,Fe3+)2(PO4)3(OH)3citations
- 2013Vibrational spectroscopic characterization of the phosphate mineral series eosphorite-childrenite-(Mn,Fe)Al(PO4)(OH)2.(H2O)citations
- 2013The phosphate mineral arrojadite-(KFe) and its spectroscopic characterizationcitations
- 2013Vibrational spectroscopic characterization of the phosphate mineral phosphophyllite - Zn2Fe(PO4)2.4H2O, from Hagendorf Sud, Germany and in comparison with other zinc phosphatescitations
- 2012Thermal analysis and application of organoclays for water purification
- 2012Raman and infrared spectroscopic characterization of beryllonite, a sodium and beryllium phosphate mineral - implications for mineral collectorscitations
- 2011Characterisation of organoclays and adsorption of p-nitrophenol: Environmental applicationcitations
- 2011Synthesis and vibrational spectroscopy of halotrichite and bilinitecitations
- 2009Thermal decomposition of hydrotalcites with variable cationic ratioscitations
- 2008Thermal decomposition of synthesized layered double hydroxides based upon Mg/(Fe,Cr) and carbonatecitations
- 2008Thermal decomposition of hydrotalcite with molybdate and vanadate anions in the interlayercitations
- 2008Characterisation of red mud and seawater neutralised red mud using vibrational spectroscopic techniques
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article
Thermal decomposition of hydrotalcite with molybdate and vanadate anions in the interlayer
Abstract
Hydrotalcites containing carbonate, vanadate and molybdate were prepared by coprecipitation. The resulting materials were characterized by XRD, and TGA/DTA to determine the stability of the hydrotalcites synthesised. The thermal decomposition of carbonate hydrotalcites consist of two decomposition steps between 300 and 400 degrees Celsius, attributed to the simultaneous dehydroxylation and de-carbonation 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, Al2O3, MgAl2O4, NaMg4(VO4)3 and Na2Mg4(MoO4)5. The presence of oxy-anions proved to be beneficial in the stability of the hydrotalcite structure, shown by the delay in dehydroxylation of oxy-anion containing hydrotalcites compared to the carbonate hydrotalcite. This is due to the substantial amount of hydroxyl groups involved in a network of hydrogen bonds involving the intercalated anions. Therefore, the stability of the hydrotalcite structure appears to be dependent on the type of anion present in the interlayer. The order of thermal stability for the synthesized hydrotalcites in this study is Syn-HT-V > Syn-HT-Mo > Syn-HT-CO3-V > Syn-HT-CO3-Mo > Syn-HT-CO3. Carbonate containing hydrotalcites prove to be less stable then oxy-anion only hydrotalcites.