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Hydrothermal synthesis and characterization of double phase magnesium vanadium oxides

Wybrane pełne teksty z tego czasopisma
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Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Purpose: The electronic conductivity of derivatives of MgxVyOz type compounds is magnitude higher than that of the vanadium oxide without magnesium. Also, magnesium containing compounds exhibit significantly improved kinetic behaviour and rate capability. In this perspective, we aim to synthesis of magnesium vanadium oxide under mild hydrothermal conditions. Design/methodology/approach: Double phase magnesium vanadium oxides were synthesized by dissolving magnesium nitrate and V2O5 in the ultra pure water with in an appropriate molar ratio. The homogeneous solution in the stainless-steel container was put into furnace and heated 3 days (72 hours) at 180ºC. The product was washed by high pure water and ethanol, dried at 70ºC for 2 hours and homogenized in an agate mortar. Then, final product was ready to analyse. Powder X-ray Diffractometer (XRD) was used to determine crystal structure of the product. FTIR spectrum was taken to support the functional groups. Thermo gravimetric-differential thermal analysis (TG/DTA) was carried out to identify thermal character. Morphological properties and semi-quantitative analyse of the sample was performed by Scanning electron microscope/Electron disperse (SEM/EDX). Phase analyse was realized by High Score Plus Program. Findings:The XRD patterns show that the product is Mg0.01V2O5 (ICDD:89-0610)-β-Mg1.9V3O8 (ICDD:23-1232). The result of phase analyse show that the sample contains %27.2 Mg0.01V2O5 and %72.8 β-Mg1.9V3O8. The mixture was obtained under mild hydrothermal conditions for the first time as distinct from literature. Characterization studies were mainly based on powder X-ray diffraction technique. Also, thermal behaviour, morphology and percentage of component were determined. Research limitations/implications:The principal of hydrothermal method is low temperature/high pressure synthesis in water. Sometimes, optimizing of the most convenient condition can be time and chemical consuming. This situation could be a limit to use hydrothermal method. But, this can eliminate with deep background. Practical implications: The compounds can find many application areas utilizing kinetic behaviour, rate capability and electronic conductivity properties. Originality/value: We achieved the hydrothermal synthesis of Mg0.01V2O5 (ICDD:89-0610)- β-Mg1.9V3O8 (ICDD:23-1232) under mild hydrothermal conditions for the first time as distinct from literature.
Rocznik
Strony
53--57
Opis fizyczny
Bibliogr. 17 poz., rys.
Twórcy
autor
  • Department of Chemistry, Faculty of Science & Art, University of Balikesir, 10145 Balikesir, Turkey
  • Department of Chemistry, Faculty of Science & Art, University of Balikesir, 10145 Balikesir, Turkey
autor
  • Department of Chemistry, Faculty of Science & Art, University of Balikesir, 10145 Balikesir, Turkey
Bibliografia
  • [1] M. Kohlmeier, Vanadium, Nutrient Metabolism, Food Science and Technology A (2003) 762-766.
  • [2] K.H. Seng, J. Liu, Z.P. Guo, Z.X. Chen, D. Jia, H.K. Liu, Free-standing V2O5 electrode for flexible lithium ion batteries, Electrochemistry Communications 13 (2011) 383-386.
  • [3] M. Eguchi, K. Ozawa, Lithium insertion property of Li22V2O5•nH2O, Electrochimica Acta 52 (2007) 2657-2660.
  • [4] H.H. Kung, M.C. Kung, Oxidative dehydrogenation of alkanes over vanadium-magnesium-oxides, Applied Catalysis A: General 157 (1997) 105-116.
  • [5] G.M. Clark, R. Morley, A study of the MgO-V2O5 system, Journal of Solid State Chemistry 16 (1976) 429-435.
  • [6] M.A. Chaar, D. Patel, M.C. Kung, H.H. Kung, Selective oxidative dehydrogenation of butane over V-Mg-O catalysts, Journal of Catalysis 105 (1987) 483-498.
  • [7] D.S.H. Sam, V. Soenen, J.C. Volta, Oxidative dehydrogenation of propane over V-Mg-O catalysts, Journal of Catalysis 123 (1990) 417-435.
  • [8] A. Corma, J.M. López Nieto, N. Paredes, Influence of preparation methods of V-Mg-O catalyst on their catalytic properties for the oxidative dehydrogenation of propane, Journal of Catalysis 144 (1993) 425-438.
  • [9] X. Gao, P. Ruiz, Q. Xin, X. Guo, B. Delmon, Effect of Coexistence of Magnesium Vanadate Phases in the Selective Oxidation of Propane to Propene, Journal of Catalysis 148 (1994) 56-67.
  • [10] J. Kijenski, A. Baiker, M. Glinsky, P. Dollenmeier, A. Wokaum, Monolayers and double layers of vanadium pentoxide on different carriers: Preparation, characterization and catalytic activities, Journal of Catalysis 101 (1986) 1-11.
  • [11] W.K. Sharma, A. Wokaum, A. Baiker, ESR characterization of vanadium pentoxide monolayers and double layers supported on various carriers, Journal of Pyhsical Chemistry 90 (1986) 2715-2718.
  • [12] M. Del Arco, M.J. Holgado, C. Martin, V. Rives, New route for the synthesis of V2O5-MgO oxidative dehydrogenation catalysts, Journal of Materials Science Letters 6 (1987) 616-619.
  • [13] J.M.L. Nieto, A. Dejoz, M.I. Vazquez, W.O. Leary, Oxidative dehydrogenation of n-butane on MgO-supported vanadium oxide catalysts, Journal of Cunningham Catalysis Today 40 (1998) 215-228.
  • [14] A. Pantazidis, A. Burrows, C.J. Kiely, C. Mirodatos, Direct evidence of active surface reconstruction during oxidative dehydrogenation of propane over V-Mg-O catalyst, Journal of Catalysis 177 (1998) 325-334.
  • [15] S.R.G. Carrazán, C. Peres, J.P. Bernard, M. Ruwet, P. Ruiz, B. Delmon, Catalytic synergy in the oxidative dehydrogenation of propane over Mg-V-O catalysts, Journal of Catalysis 158 (1996) 452-476.
  • [16] M.I. Khan, T. Hope, S. Tabassum, Synthesis, reactivity, X-ray structure and thermal study of the mixed- metal oxide hydrate [Mn(H2O)2V2O6], Solid State Science 1 (1999) 163-178.
  • [17] K. Nakamoto, Infrared and Raman Spectra of Inorganic and Coordination Compounds. A Willey-Interscience Publication, John Wiley and Sons, 1986.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-03cb6e93-d90d-4ab3-a4f6-4ec972bc57d6
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