Dzivenko, Dmytro (2009)
High-pressure synthesis, structure and properties of cubic zirconium(IV)- and hafnium(IV) nitrides.
Technische Universität Darmstadt
Dissertation, Erstveröffentlichung
Kurzbeschreibung (Abstract)
This thesis is concerned with recently discovered high-pressure (HP) zirconium- and hafnium nitrides having cubic Th3P4-type structure, c-M3N4 (M=Zr or Hf). These compounds belong to a rapidly growing group of new hard HP nitrides exhibiting advanced properties. The research was focused on (i) synthesis of macroscopic amounts of c-M3N4, (ii) investigation of their solid state structure, composition and morphology and (iii) measurement of properties related to potential industrial applications of these compounds as hard wear-resistant materials. Nitrogen-rich starting materials for high-pressure high-temperature (HP/HT) synthesis of c-M3N4, namely nanocrystalline powders of M3N4+x with distorted NaCl-type structure, had to be prepared in this work because they were not commercially available. They were obtained via HT ammonolysis of the corresponding metal dialkylamides, M[N(C2H5)2]4, at moderate temperatures up to 873 K. Both, c-Zr3N4 and c-Hf3N4, were synthesized from the nanocrystalline M3N4+x powders applying a pressure of 12 GPa and a temperature of 1873 K using a multi-anvil HP-apparatus. The products were characterized using various techniques including powder XRD (Rietveld refinement), TEM, EPMA, SEM/EDX and Raman spectroscopy. In the case of zirconium nitride, formation of a single phase crystalline material was verified by both XRD and TEM. The presence of a small amount of oxygen in the sample, revealed by EPMA, suggested the formation of oxygen-bearing zirconium(IV) nitride (or oxynitride) having Th3P4-type structure, c-Zr2.86(N0.88O0.12)4. The measured composition was found to correspond to the general formula Zr3-u(N1-uOu)4 which fulfils the electrical neutrality condition. A high quality of the Rietveld structure refinement of the powder XRD data for c-Zr2.86(N0.88O0.12)4 supported the above findings. Further, the assignment of the structure of the obtained oxygen-bearing zirconium nitride to the Th3P4-type was confirmed by Raman spectroscopic measurements. In contrast to zirconium nitride, a minor oxidation of the hafnium nitride sample led to formation of a mixture of oxygen-poor c-Hf3N4 and an oxidic material. The latter was evident from the XRD, EPMA, and SEM/EDX measurements. A detailed analysis of the powder XRD patterns and Rietveld refinement suggested that the oxidic material is comprised of a mixture of the known γ-Hf2N2O and oI-HfO2. The last part of the thesis concerned the investigation of the properties of the synthesized materials. The bulk moduli of c-Zr2.86(N0.88O0.12)4 and c-Hf3N4 were determined via their quasi-hydrostatic compression in a diamond anvil cell up to 45 GPa. The obtained values are B0=219 GPa (B'0=4.4) and B0=227 GPa (B'0=5.3) for c-Zr2.86(N0.88O0.12)4 and c-Hf3N4, respectively. The reduced elastic modulus, Er=224 GPa, of porous c-Zr2.86(N0.88O0.12)4 (volume fraction porosity of 0.3) was measured using nanoindentation techniques. Combining B0 and Er values, the lower limits of the shear modulus G0=96 GPa, and of the Young’s modulus E0=252 GPa were determined for the oxygen-bearing c-Zr3N4. The nanoindentation hardness and Vickers microhardness, HV(1), of the porous zirconium nitride sample were measured to be 18 GPa and 12 GPa, respectively. Using a relation between hardness and volume fraction porosity, suggested in the literature, the HV(1) of the fully dense c-Zr3N4 was estimated to exceed 25 GPa. The indentation fracture toughness of 3.2 MPa m^1/2 for porous c-Zr2.86(N0.88O0.12)4 was evaluated from the Vickers indentation cracks. The linear thermal expansion coefficient of the oxygen-bearing c-Zr3N4 was found to increase from 6.6×10^6 1/K at room temperature to about 14×10^6 1/K at 873 K. Onset of the material oxidation in air was observed at 773 K. Finally, the obtained results were compared with existing experimental and theoretical data for c-M3N4 and for other related technological materials and discussed with respect to potential industrial applications of c-M3N4.
Typ des Eintrags: | Dissertation | ||||
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Erschienen: | 2009 | ||||
Autor(en): | Dzivenko, Dmytro | ||||
Art des Eintrags: | Erstveröffentlichung | ||||
Titel: | High-pressure synthesis, structure and properties of cubic zirconium(IV)- and hafnium(IV) nitrides | ||||
Sprache: | Englisch | ||||
Referenten: | Riedel, Prof. Dr. Ralf ; Fueß, Prof. Dr.- Hartmut | ||||
Publikationsjahr: | 7 August 2009 | ||||
Datum der mündlichen Prüfung: | 17 Dezember 2008 | ||||
URL / URN: | urn:nbn:de:tuda-tuprints-18742 | ||||
Kurzbeschreibung (Abstract): | This thesis is concerned with recently discovered high-pressure (HP) zirconium- and hafnium nitrides having cubic Th3P4-type structure, c-M3N4 (M=Zr or Hf). These compounds belong to a rapidly growing group of new hard HP nitrides exhibiting advanced properties. The research was focused on (i) synthesis of macroscopic amounts of c-M3N4, (ii) investigation of their solid state structure, composition and morphology and (iii) measurement of properties related to potential industrial applications of these compounds as hard wear-resistant materials. Nitrogen-rich starting materials for high-pressure high-temperature (HP/HT) synthesis of c-M3N4, namely nanocrystalline powders of M3N4+x with distorted NaCl-type structure, had to be prepared in this work because they were not commercially available. They were obtained via HT ammonolysis of the corresponding metal dialkylamides, M[N(C2H5)2]4, at moderate temperatures up to 873 K. Both, c-Zr3N4 and c-Hf3N4, were synthesized from the nanocrystalline M3N4+x powders applying a pressure of 12 GPa and a temperature of 1873 K using a multi-anvil HP-apparatus. The products were characterized using various techniques including powder XRD (Rietveld refinement), TEM, EPMA, SEM/EDX and Raman spectroscopy. In the case of zirconium nitride, formation of a single phase crystalline material was verified by both XRD and TEM. The presence of a small amount of oxygen in the sample, revealed by EPMA, suggested the formation of oxygen-bearing zirconium(IV) nitride (or oxynitride) having Th3P4-type structure, c-Zr2.86(N0.88O0.12)4. The measured composition was found to correspond to the general formula Zr3-u(N1-uOu)4 which fulfils the electrical neutrality condition. A high quality of the Rietveld structure refinement of the powder XRD data for c-Zr2.86(N0.88O0.12)4 supported the above findings. Further, the assignment of the structure of the obtained oxygen-bearing zirconium nitride to the Th3P4-type was confirmed by Raman spectroscopic measurements. In contrast to zirconium nitride, a minor oxidation of the hafnium nitride sample led to formation of a mixture of oxygen-poor c-Hf3N4 and an oxidic material. The latter was evident from the XRD, EPMA, and SEM/EDX measurements. A detailed analysis of the powder XRD patterns and Rietveld refinement suggested that the oxidic material is comprised of a mixture of the known γ-Hf2N2O and oI-HfO2. The last part of the thesis concerned the investigation of the properties of the synthesized materials. The bulk moduli of c-Zr2.86(N0.88O0.12)4 and c-Hf3N4 were determined via their quasi-hydrostatic compression in a diamond anvil cell up to 45 GPa. The obtained values are B0=219 GPa (B'0=4.4) and B0=227 GPa (B'0=5.3) for c-Zr2.86(N0.88O0.12)4 and c-Hf3N4, respectively. The reduced elastic modulus, Er=224 GPa, of porous c-Zr2.86(N0.88O0.12)4 (volume fraction porosity of 0.3) was measured using nanoindentation techniques. Combining B0 and Er values, the lower limits of the shear modulus G0=96 GPa, and of the Young’s modulus E0=252 GPa were determined for the oxygen-bearing c-Zr3N4. The nanoindentation hardness and Vickers microhardness, HV(1), of the porous zirconium nitride sample were measured to be 18 GPa and 12 GPa, respectively. Using a relation between hardness and volume fraction porosity, suggested in the literature, the HV(1) of the fully dense c-Zr3N4 was estimated to exceed 25 GPa. The indentation fracture toughness of 3.2 MPa m^1/2 for porous c-Zr2.86(N0.88O0.12)4 was evaluated from the Vickers indentation cracks. The linear thermal expansion coefficient of the oxygen-bearing c-Zr3N4 was found to increase from 6.6×10^6 1/K at room temperature to about 14×10^6 1/K at 873 K. Onset of the material oxidation in air was observed at 773 K. Finally, the obtained results were compared with existing experimental and theoretical data for c-M3N4 and for other related technological materials and discussed with respect to potential industrial applications of c-M3N4. |
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Alternatives oder übersetztes Abstract: |
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Freie Schlagworte: | high pressure, zirconium nitride, hafnium nitride, Th3P4-type structure, elastic moduli, hardness, multi-anvil, diamond anvil cell | ||||
Sachgruppe der Dewey Dezimalklassifikatin (DDC): | 500 Naturwissenschaften und Mathematik > 500 Naturwissenschaften 600 Technik, Medizin, angewandte Wissenschaften > 620 Ingenieurwissenschaften und Maschinenbau |
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Fachbereich(e)/-gebiet(e): | 11 Fachbereich Material- und Geowissenschaften 11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft 11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft > Fachgebiet Disperse Feststoffe |
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Hinterlegungsdatum: | 09 Sep 2009 11:26 | ||||
Letzte Änderung: | 17 Jul 2018 07:54 | ||||
PPN: | |||||
Referenten: | Riedel, Prof. Dr. Ralf ; Fueß, Prof. Dr.- Hartmut | ||||
Datum der mündlichen Prüfung / Verteidigung / mdl. Prüfung: | 17 Dezember 2008 | ||||
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