Conformation of the cycloalkanes C14H28, C16H32, and C22H44 in the liquid and high-temperature crystalline phases by vibrational spectroscopy

1989 ◽  
Vol 111 (6) ◽  
pp. 1947-1958 ◽  
Author(s):  
V. L. Shannon ◽  
H. L. Strauss ◽  
Robert G. Snyder ◽  
C. A. Elliger ◽  
W. L. Mattice
Keyword(s):  
High Temperature ◽  
Vibrational Spectroscopy ◽  
Crystalline Phases

The model rotator phase

1988 ◽  
Vol 53 (5) ◽  
pp. 889-902
Author(s):  
Josef Šebek
Keyword(s):  
High Temperature ◽  
Partition Function ◽  
Conformational Flexibility ◽  
Small Probability ◽  
Crystalline Phases ◽  
Rotator Phase

It is shown that the formation of the so-called rotator phase of alkanes (one of the high temperature crystalline phases) might be connected with a partial increase of the conformational flexibility of chains. The conformations with higher number of kinks per chain, which have been neglected till now, are shown to contribute effectively to the conformational partition function. Small probability of these states given by the Boltzmann exponent is compensated by a large number of ways in which they can be distributed along the chain. The deduced features of the rotator phase seem to be in agreement with the experimentally observed properties.

Formation of New Crystalline Phases upon High-Temperature Annealing of Iron Borate FeBO3 in Different Gas Media

JETP Letters ◽  
2020 ◽  
Vol 112 (6) ◽  
pp. 352-356
Author(s):  
N. I. Snegirev ◽  
I. S. Lyubutin ◽  
S. V. Yagupov ◽  
A. G. Kulikov ◽  
V. V. Artemov ◽  
...  
Keyword(s):  
High Temperature ◽  
High Temperature Annealing ◽  
Iron Borate ◽  
Crystalline Phases

Crystal-chemistry and vibrational spectroscopy of ferrinatrite, Na3[Fe(SO4)3]·3H2O, and its high-temperature decomposition

2018 ◽  
Vol 46 (2) ◽  
pp. 119-131 ◽  
Author(s):  
Gennaro Ventruti ◽  
Giancarlo Della Ventura ◽  
Maria Lacalamita ◽  
Marco Sbroscia ◽  
Armida Sodo ◽  
...  
Keyword(s):  
High Temperature ◽  
Crystal Chemistry ◽  
Vibrational Spectroscopy ◽  
Temperature Decomposition

A DTA Study on HVOF Thermally Sprayed WC–M Coatings

2007 ◽  
Vol 566 ◽  
pp. 155-160
Author(s):  
M. Heydarzadeh Sohi ◽  
Shahin Khameneh Asl ◽  
Kazuyuki Hokamoto ◽  
M. Rezvani
Keyword(s):  
Heat Treatment ◽  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
High Temperature ◽  
Amorphous Phase ◽  
Exothermic Reaction ◽  
Intermetallic Phase ◽  
Chemical Compositions ◽  
Crystalline Phases ◽  
Sprayed Coatings

Five types of tungsten carbide based powders with different chemical compositions (WC-12Co, WC-17Co, WC-10Ni, WC-10Co-4Cr and WC- 20Cr-7Ni) were deposited onto ST37 mild steel substrate using high velocity oxy fuel (HVOF) spray technique. The feedstock powders and sprayed coatings were studied by using X-ray diffraction (XRD), and differential thermal analyzing (DTA). The results were shown during HVOF thermal spraying, WC-M powders become partially melted before being sprayed on the surface of the substrate with supersonic speed. In these types of coatings, the crystallographic structures are normally non equilibrium, because the cooling rates of the deposited splats are very high due to the cold substrate acting as a thermal sink. These partially melted powders are then rapidly solidified to an amorphous phase. XRD analysis showed that the amorphous phase was existed in all of the as sprayed coatings. The amorphous phase in WC-12Co, WC-17Co and WC-10Ni coatings was transformed to crystalline phases by heat treatment at high temperature. Heat treatment of these coatings at high temperature also resulted in partially dissolution of WC particles and formation of new crystalline phases. In cobalt base coatings, the new phases were eta carbide phases like Co6W6C and Co3W3C but in WC-10Ni coating a NiW intermetallic phase was formed. Heat treatment of WC-10Co-4Cr and WC-20Cr-7Ni coatings did not change the amorphous phases in these coatings. Differential thermal analysis of cobalt containing coatings revealed an exothermic reaction at approximately 880°C. This exothermic reaction may be related to the transformation of the amorphous phase to eta phases. On the contrary, DTA analysis of feedstock powders of these coatings showed an endothermic reaction at approximately 1000°C. DTA analyses of nickel containing cermets also showed similar results. Differential thermal analysis of chromium containing cermets did not show any noticeable exothermic or endothermic reactions.

Crystalline Phases During the Melting of Bi2Sr2CaCu2OX

1991 ◽  
Vol 249 ◽  
Author(s):  
Ming Xu ◽  
J. Polonka ◽  
A. I. Goldman ◽  
D. K. Finnemore ◽  
Qiang Li ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
High Temperature ◽  
Energy Dispersive Spectroscopy ◽  
Energy Dispersive ◽  
Crystalline Phases ◽  
Fast Cooling ◽  
Crystallization From The Melt ◽  
Scanning Electron

ABSTRACTThe melting of Bi2Sr2CaCu2Ox material has been studied by scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) in order to study the phases that formed in the high temperature regions. Two distinct phases of (Sr1-xCax)CuO2 and (Sr1-xCax)2CuO3 have been observed in the Bi-rich matrix depending upon quenching temperatures. Crystallization from the melt by fast cooling usually produce the co-existence of Bi (2201) and these Sr-Ca-Cu-O phases.

scholarly journals β-Eu(BO2)3 – a new member of the β-RE(BO2)3 (RE=Y, Nd, Sm, Gd–Lu) structure family

2019 ◽  
Vol 74 (9) ◽  
pp. 685-692 ◽  
Author(s):  
Birgit Fuchs ◽  
Hubert Huppertz
Keyword(s):  
High Pressure ◽  
High Temperature ◽  
Vibrational Spectroscopy ◽  
Powder Diffraction ◽  
Title Compound ◽  
Line Emission ◽  
Orthorhombic Space Group ◽  
X Ray ◽  
High Pressure High Temperature ◽  
Temperature Experiment

AbstractThe title compound β-Eu(BO2)3 was synthesized in a high-pressure/high-temperature experiment at 4 GPa and 1473 K. The europium borate crystallizes in the orthorhombic space group Pnma (no. 62) with the lattice parameters a = 16.071(2), b = 7.440(4), and c = 12.362(5) Å. The structure is isotypic to the already known meta-borates β-RE(BO2)3 (RE = Y, Nd, Sm, Gd, Dy–Lu) and is built up of approximately triangular ribbons of BO4 tetrahedra. The compound was further characterized by X-ray powder diffraction, vibrational spectroscopy and shows a typical Eu3+ line emission upon excitation at 448 nm.

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