High-Pressure, High-Temperature Formation of Phase-Pure Monoclinic Zirconia Nanocrystals Studied by Time-Resolved in situ Synchrotron X-Ray Diffraction

2009 ◽  
Vol 21 (35) ◽  
pp. 3572-3575 ◽  
Author(s):  
Martin Bremholm ◽  
Jacob Becker-Christensen ◽  
Bo Brummerstedt Iversen
Keyword(s):  
High Pressure ◽  
High Temperature ◽  
Monoclinic Zirconia ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
X Ray ◽  
High Pressure High Temperature ◽  
Phase Pure

Crystal structure of a high-pressure/high-temperature phase of alumina by in situ X-ray diffraction

2004 ◽  
Vol 3 (6) ◽  
pp. 389-393 ◽  
Author(s):  
Jung-Fu Lin ◽  
Olga Degtyareva ◽  
Charles T. Prewitt ◽  
Przemyslaw Dera ◽  
Nagayoshi Sata ◽  
...  
Keyword(s):  
Crystal Structure ◽  
High Pressure ◽  
High Temperature ◽  
High Temperature Phase ◽  
Temperature Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Pressure High Temperature

scholarly journals High-pressure synthesis and crystal structure of the mixed-cation borate Ga4In4B15O33(OH)3

2019 ◽  
Vol 74 (4) ◽  
pp. 357-363
Author(s):  
Daniela Vitzthum ◽  
Hubert Huppertz
Keyword(s):  
Crystal Structure ◽  
High Pressure ◽  
High Temperature ◽  
Diffraction Data ◽  
X Ray Diffraction ◽  
Synthesis And Crystal Structure ◽  
X Ray ◽  
Mixed Cation ◽  
High Pressure High Temperature ◽  
Pressure Synthesis

AbstractThe mixed cation triel borate Ga4In4B15O33(OH)3 was synthesized in a Walker-type multianvil apparatus at high-pressure/high-temperature conditions of 12.5 GPa and 1300°C. Although the product could not be reproduced in further experiments, its crystal structure could be reliably determined via single-crystal X-ray diffraction data. Ga4In4B15O33(OH)3 crystallizes in the tetragonal space group I41/a (origin choice 2) with the lattice parameters a = 11.382(2), c = 15.244(2) Å, and V = 1974.9(4) Å3. The structure of the quaternary triel borate consists of a complex network of BO4 tetrahedra, edge-sharing InO6 octahedra in dinuclear units, and very dense edge-sharing GaO6 octahedra in tetranuclear units.

scholarly journals High-pressure synthesis and characterization of the non-centrosymmetric scandium borate ScB6O9(OH)3

2020 ◽  
Vol 75 (6-7) ◽  
pp. 597-603
Author(s):  
Birgit Fuchs ◽  
Hubert Huppertz
Keyword(s):  
High Pressure ◽  
High Temperature ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Pressure High Temperature ◽  
Structure Solution ◽  
Temperature Experiment ◽  
Pressure Synthesis

AbstractThe non-centrosymmetric scandium borate ScB6O9(OH)3 was obtained through a high-pressure/high-temperature experiment at 6 GPa and 1473 K. Single-crystal X-ray diffraction revealed that the structure is isotypic to InB6O9(OH)3 containing borate triple layers separated by scandium layers. The compound crystallizes in the space group Fdd2 with the lattice parameters a = 38.935(4), b = 4.4136(4), and c = 7.6342(6) Å. Powder X-ray diffraction and vibrational spectroscopy were used to further characterize the compound and verify the proposed structure solution.

The high-pressure cadmium borate Cd6B22O39·H2O

2015 ◽  
Vol 70 (3) ◽  
pp. 183-190 ◽  
Author(s):  
Gerhard Sohr ◽  
Nina Ciaghi ◽  
Klaus Wurst ◽  
Hubert Huppertz
Keyword(s):  
High Pressure ◽  
High Temperature ◽  
Structural Characteristics ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Pressure High Temperature ◽  
Cell Dimensions ◽  
Temperature Experiment ◽  
Unit Cell Dimensions ◽  
Ir And Raman

AbstractSingle crystals of the hydrous cadmium borate Cd6B22O39·H2O were obtained through a high-pressure/high-temperature experiment at 4.7 GPa and 1000 °C using a Walker-type multianvil apparatus. CdO and partially hydrolyzed B2O3 were used as starting materials. A single crystal X-ray diffraction study has revealed that the structure of Cd6B22O39·H2O is similar to that of the type M6B22O39·H2O (M=Fe, Co). Layers of corner-sharing BO4 groups are interconnected by BO3 groups to form channels containing the metal cations, which are six- and eight-fold coordinated by oxygen atoms. The compound crystallizes in the space group Pnma (no. 62) [R1=0.0379, wR2=0.0552 (all data)] with the unit cell dimensions a=1837.79(5), b=777.92(2), c=819.08(3) pm, and V=1171.00(6) Å3. The IR and Raman spectra reflect the structural characteristics of Cd6B22O39·H2O.

In-situ X-ray diffraction study on β-CrOOH at high pressure and high-temperature

2019 ◽  
Vol 39 (3) ◽  
pp. 499-508 ◽  
Author(s):  
Chikara Shito ◽  
Keitaro Okamoto ◽  
Yuki Sato ◽  
Ryuji Watanabe ◽  
Tomonori Ohashi ◽  
...  
Keyword(s):  
High Pressure ◽  
High Temperature ◽  
Diffraction Study ◽  
X Ray Diffraction ◽  
X Ray

scholarly journals Low-Power Laser Graphitization of High Pressure—High Temperature Nanodiamond Films

2020 ◽  
Vol 10 (9) ◽  
pp. 3329
Author(s):  
Konstantin G. Mikheev ◽  
Tatyana N. Mogileva ◽  
Arseniy E. Fateev ◽  
Nicholas A. Nunn ◽  
Olga A. Shenderova ◽  
...  
Keyword(s):  
High Pressure ◽  
High Temperature ◽  
Laser Excitation ◽  
X Ray Diffraction ◽  
Power Laser ◽  
Green Luminescence ◽  
X Ray ◽  
Atomic Force ◽  
High Pressure High Temperature ◽  
Before And After

Laser-induced graphitization of 100 nm monocrystals of diamond particles synthesized by high-pressure high-temperature (HP-HT) methods is not typically observed. The current study demonstrates the graphitization of 150 nm HP-HT nanodiamond particles in ca. 20-μm-thick thin films formed on a glass substrate when the intensity of a focused 633 nm He-Ne laser exceeds a threshold of ~ 33 kW/cm2. Graphitization is accompanied by green luminescence. The structure and morphology of the samples were investigated before and after laser excitation while using X-ray diffraction (XRD), Raman spectroscopy, atomic force (AFM), and scanning electron microscopy (SEM). These observations are explained by photoionization of [Ni-N]- and [N]-centers, leading to the excitation of electrons to the conduction band of the HP-HT nanodiamond films and an increase of the local temperature of the sample, causing the transformation of sp3 HP-HT nanodiamonds to sp2-carbon.

Kinetics of high-pressure mineral phase transformations using in situ time-resolved X-ray diffraction in the Paris-Edinburgh cell: a practical guide for data acquisition and treatment

2008 ◽  
Vol 72 (2) ◽  
pp. 683-695 ◽  
Author(s):  
J. P. Perrillat
Keyword(s):  
High Pressure ◽  
Phase Transformations ◽  
Kinetic Studies ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
X Ray ◽  
Practical Guide ◽  
Set Up ◽  
Isothermal Kinetic

AbstractSynchrotron X-ray diffraction (XRD) is a powerful technique to study in situ and in real-time the structural and kinetic processes of pressure-induced phase transformations. This paper presents the experimental set-up developed at beamline ID27 of the ESRF to perform time-resolved angle dispersive XRD in the Paris-Edinburgh cell. It provides a practical guide for the acquisition of isobaric-isothermal kinetic data and the construction of transformation-time plots. The interpretation of experimental data in terms of reaction mechanisms and transformation rates is supported by an overview of the kinetic theory of solid-solid transformations, with each step of data processing illustrated by experimental results of relevance to the geosciences. Reaction kinetics may be affected by several factors such as the sample microstructure, impurities or differential stress. Further high-pressure kinetic studies should investigate the influence of such processes, in order to acquire kinetic information more akin to natural or technological processes.

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