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Study of the reaction mechanisms involved in the formation of zirconium oxycarbide from Metal-Organic Frameworks (MOFs) precursors

Zirconium-based Metal-Organic Frameworks (MOF) precursors were used to synthesize nanopowders of ZrCxOy zirconium oxycarbide. The reaction mechanisms involved in the thermal transformation of two different MOF precursors obtained by using fumaric (H2FUM) and terephthalic (H2BDC) acid as linkers were...

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Published in:Journal of alloys and compounds 2016-09, Vol.680, p.571-585
Main Authors: David, Jeremy, Trolliard, Gilles, Volkringer, Christophe, Loiseau, Thierry, Masson, Olivier, Maître, Alexandre
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description Zirconium-based Metal-Organic Frameworks (MOF) precursors were used to synthesize nanopowders of ZrCxOy zirconium oxycarbide. The reaction mechanisms involved in the thermal transformation of two different MOF precursors obtained by using fumaric (H2FUM) and terephthalic (H2BDC) acid as linkers were investigated. The transformation of these two precursors, characterized by two different C/Zr ratio proceeds through an intermediate zirconia phase formed during heating, in association with turbostratic carbon. The zirconia is shown to nucleate within carbon areas coming from the decomposition of the precursors. Zirconia is mainly observed under its tetragonal form in the Zr-BDC carbon rich system (C/Zr = 8) while the monoclinic form predominates in the Zr-FUM low carbon system (C/Zr = 4). The transformation then finally appears very similar to the classical carbothermal reaction between zirconia and carbon black. The reconstructive transformation of zirconia into an oxycarbide phase being highly energy consuming, high temperature heat treatment are required precluding the possibility to obtain the expected nanocrystalline oxycarbide phase by such a way of synthesis. Coupled XRD and TEM study reveals that Zr-BDC system is considered as carbon saturated and the Zr-FUM system appears as carbon deficient. In the Zr-BDC system, zirconia first disappears during the thermal reaction and the oxygen rich oxycarbide that is first formed then reacts with residual carbon to provide progressive carbon enrichment until the saturation of the ZrCxOy oxycarbide solid solution. On the opposite, in the Zr-FUM system, the carbon is the rate-limiting factor of the reaction and the residual zirconia is shown to react with the oxycarbide earlier formed, suggesting the occurrence of a peritectoid like transformation. [Display omitted] •Oxycarbide compounds were obtained directly from Metal Oxide Frameworks precursors.•The transformation of two different precursors was studied by TEM, XRD and ATD.•The transformation involves the formation of an intermediate zirconia phase.•The reaction mechanisms involved are likely to those of the carbothermal reaction.
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The reconstructive transformation of zirconia into an oxycarbide phase being highly energy consuming, high temperature heat treatment are required precluding the possibility to obtain the expected nanocrystalline oxycarbide phase by such a way of synthesis. Coupled XRD and TEM study reveals that Zr-BDC system is considered as carbon saturated and the Zr-FUM system appears as carbon deficient. In the Zr-BDC system, zirconia first disappears during the thermal reaction and the oxygen rich oxycarbide that is first formed then reacts with residual carbon to provide progressive carbon enrichment until the saturation of the ZrCxOy oxycarbide solid solution. On the opposite, in the Zr-FUM system, the carbon is the rate-limiting factor of the reaction and the residual zirconia is shown to react with the oxycarbide earlier formed, suggesting the occurrence of a peritectoid like transformation. 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The reaction mechanisms involved in the thermal transformation of two different MOF precursors obtained by using fumaric (H2FUM) and terephthalic (H2BDC) acid as linkers were investigated. The transformation of these two precursors, characterized by two different C/Zr ratio proceeds through an intermediate zirconia phase formed during heating, in association with turbostratic carbon. The zirconia is shown to nucleate within carbon areas coming from the decomposition of the precursors. Zirconia is mainly observed under its tetragonal form in the Zr-BDC carbon rich system (C/Zr = 8) while the monoclinic form predominates in the Zr-FUM low carbon system (C/Zr = 4). The transformation then finally appears very similar to the classical carbothermal reaction between zirconia and carbon black. The reconstructive transformation of zirconia into an oxycarbide phase being highly energy consuming, high temperature heat treatment are required precluding the possibility to obtain the expected nanocrystalline oxycarbide phase by such a way of synthesis. Coupled XRD and TEM study reveals that Zr-BDC system is considered as carbon saturated and the Zr-FUM system appears as carbon deficient. In the Zr-BDC system, zirconia first disappears during the thermal reaction and the oxygen rich oxycarbide that is first formed then reacts with residual carbon to provide progressive carbon enrichment until the saturation of the ZrCxOy oxycarbide solid solution. On the opposite, in the Zr-FUM system, the carbon is the rate-limiting factor of the reaction and the residual zirconia is shown to react with the oxycarbide earlier formed, suggesting the occurrence of a peritectoid like transformation. 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identifier ISSN: 0925-8388
ispartof Journal of alloys and compounds, 2016-09, Vol.680, p.571-585
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subjects Carbon
Chemical Sciences
Coordination chemistry
Inorganic chemistry
Material chemistry
Metal-Organic Frameworks
Oxycarbides
Phase transformations
Precursors
Reaction mechanisms
Transformations
Transmission Electron Microscopy
Zirconium
Zirconium (oxy) carbide
Zirconium dioxide
title Study of the reaction mechanisms involved in the formation of zirconium oxycarbide from Metal-Organic Frameworks (MOFs) precursors
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