ChemInform Abstract: Chemical Dynamics and Phase Transformation in High Temperature Processes Using Time-Resolved and Spatially Resolved X-Ray Diffraction

ChemInform ◽  
2010 ◽  
Vol 33 (46) ◽  
pp. no-no
Author(s):  
Joe Wong
Keyword(s):  
Phase Transformation ◽  
High Temperature ◽  
Chemical Dynamics ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
X Ray ◽  
Spatially Resolved ◽  
High Temperature Processes

Influence of Mn and Ni on Austenite Stabilization during a High Temperature Q&P Treatment

2021 ◽  
Vol 1016 ◽  
pp. 379-384
Author(s):  
Eider Del Molino ◽  
Teresa Gutierrez ◽  
Mónica Serna-Ruiz ◽  
Maribel Arribas ◽  
Artem Arlazarov
Keyword(s):  
Phase Transformation ◽  
Electron Microscope ◽  
High Temperature ◽  
Retained Austenite ◽  
Nickel Content ◽  
X Ray Diffraction ◽  
Quenching And Partitioning ◽  
X Ray ◽  
Scanning Electron ◽  
P Cycle

The aim of this work was to study the influence of quenching and partitioning temperatures combined with various levels of Mn and Ni contents on the austenite stabilization along the quenching and partitioning (Q&P) cycle. Three steels with 2 wt.%, 4 wt.% and 6 wt.% manganese and one steel with 2 wt.% nickel content were investigated. Phase transformation temperatures and critical cooling rates were obtained experimentally using dilatometer for each alloy. Q&P cycles with different quenching and partitioning temperatures were also done in dilatometer, thus, allowing monitoring of the expansion/contraction during the whole Q&P cycle. Microstructure characterization was performed by means of a Scanning Electron Microscope and X-Ray Diffraction to measure retained austenite content. It was found that, strongly depending on the Q&P conditions, austenite stabilization or decomposition occurs during partitioning and final cooling. In case of high partitioning temperature cycles, austenite reverse transformation was observed. Certain cycles resulted in a very effective austenite stabilization and interesting microstructure.

Displacive Phase Transformation in Vanadium - Substituted Lanthanum Niobate

1983 ◽  
Vol 24 ◽  
Author(s):  
A. T. Aldred ◽  
S.-K. Chan ◽  
M. H. Grimsditch ◽  
M. V. Nevitt
Keyword(s):  
Phase Transformation ◽  
High Temperature ◽  
Low Temperature ◽  
Raman Scattering ◽  
Transformation Temperature ◽  
Complex Oxides ◽  
Temperature Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
First Order

ABSTRACTThe displacive transformations in complex oxides of the type LaNb1-xVxO4 has been studied by x-ray diffraction and Raman scattering for 0 < x < 0.3. X-ray diffraction results indicate that the transformation from the tetragonal high temperature structure (C4h6) to the monoclinic low-temperature structure (C2h6) is higher than first order and that the transformation temperature Tc is depressed significantly by V substitution. Raman scattering results show that the force constant between the nearest (Nb, V)O4 tetrahedral units behave uniquely compared to others. It softens at Tc as a function of composition and it also softens as a function of temperature as Tc is approached from above.

Behaviors of the Zr–1.0Sn–0.39Nb–0.31Fe–0.05Cr Alloy at High Temperature

2011 ◽  
Vol 399-401 ◽  
pp. 80-84
Author(s):  
Yi Yuan Tang ◽  
Jie Li Meng ◽  
Kai Lian Huang ◽  
Jian Lie Liang
Keyword(s):  
Thermal Expansion ◽  
Phase Transformation ◽  
High Temperature ◽  
Oxide Film ◽  
Room Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Thin Oxide Film ◽  
Thermal Expansion Coefficients ◽  
Expansion Coefficients

Phase transformation of the Zr-1.0Sn-0.39Nb-0.31Fe-0.05Cr alloy was investigated by high temperature X-ray diffraction (XRD). The XRD results revealed that the alloy contained two precipitates at room temperature, namely β-Nb and hexagonal Zr(Nb,Fe,Cr,)2. β-Nb was suggested to dissolve into the α-Zr matrix at the 580oC. Thin oxide film formed at the alloy’s surface was identified as mixture of the monoclinic Zr0.93O2and tetragonal ZrO2, when the temperature reached to 750oC and 850 oC. The thermal expansion coefficients of αZr in this alloy was of αa = 8.39×10-6/°C, αc = 2.48×10-6/°C.

A furnace for the in situ study of the formation of inorganic solids at high temperature using time-resolved energy-dispersive x-ray diffraction

2000 ◽  
Vol 71 (11) ◽  
pp. 4177 ◽  
Author(s):  
Margret J. Geselbracht ◽  
Richard I. Walton ◽  
E. Sarah Cowell ◽  
Franck Millange ◽  
Dermot O’Hare
Keyword(s):  
High Temperature ◽  
Energy Dispersive ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
X Ray ◽  
Inorganic Solids ◽  
In Situ Study

A time-resolved x-ray diffraction study of Ti5Si3 product formation during combustion synthesis

1997 ◽  
Vol 12 (12) ◽  
pp. 3230-3240 ◽  
Author(s):  
C. R. Kachelmyer ◽  
I. O. Khomenko ◽  
A. S. Rogachev ◽  
A. Varma
Keyword(s):  
Thermal Expansion ◽  
High Temperature ◽  
Product Formation ◽  
X Ray Diffraction ◽  
Temperature Synthesis ◽  
Time Resolved ◽  
X Ray ◽  
Thermal Expansion Coefficients ◽  
High Temperature Synthesis ◽  
Expansion Coefficients

Time-resolved x-ray diffraction (TRXRD) was performed during Ti5Si3 synthesis by the self-propagating high-temperature synthesis mode for different Ti size fractions. It was determined that the time for product formation (ca. 15 s) was independent of Ti particle size. However, the formation of Ti5Si4 phase occurred when relatively large titanium particles were used. A simultaneous measurement of the temperature and TRXRD allowed us to attribute the shifting of XRD peaks at high temperature to thermal expansion of the Ti5Si3 product. The thermal expansion coefficients differ for different crystal planes, and their numerical values compare well with those reported previously in the literature.

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