Liquid state properties and solidification features of the pseudo binary BaS-La2S3

The high temperature thermodynamic properties of chalcogenides materials based on BaS remain elusive. Herein the pseudo binary BaS-La2S3 is investigated above 1573 K. The liquid properties of BaS-La2S3 are measured by means of high resolution in-situ visualization coupled with thermal arrest measurements in a thermal imaging furnace. This enables to report the first observation of such melts in a container-less setting. The melting points of BaS and La2S3 are revisited at 2454 K and 2004 K respectively. La2S3 demonstrates a high stability in its liquid state, in strike difference with the sublimation observed for BaS. BaS is however partially stabilized with the addition of few percents of La2S3. The remarkable chemical and thermal stability of La2S3-rich samples contrasts with the partial decomposition and high vapor pressure observed for BaS-rich samples. Observations and analysis of the solidified samples suggest three different solid solutions. Solid and liquid densities are investigated along the different compositions, supporting a first estimate of the volumetric thermal expansion coefficient for La2S3.

Liquid State Properties and Solidification Features of the Pseudo Binary BaS-La2S3

The high temperature thermodynamic properties of chalcogenides materials based on BaS remain elusive, and herein the La2S3 pseudo binary system is investigated above 1573 K. The liquid properties of BaS-La2S3 are measured by means of high resolution in-situ visualization coupled with thermal arrest measurements in a thermal imaging furnace. This enables to report for the first observation of such melts in a containerless setting. The melting points of BaS and La2S3 are revisited at 2454 K and 2004 K respectively. La2S3 demonstrates a high stability in its liquid state, in strike difference with the sublimation observed for BaS. BaS is however partially stabilized with the addition of few percents of La2S3.The remarkable chemical and thermal stability of La2S3-rich samples, contrasts with the partial decomposition and high vapor pressure observed for BaS-rich samples. Observations and analysis of the solidified samples suggests three different solid solutions. Solid and liquid densities are investigated along the different compositions, supporting a first estimate of the volumetric thermal expansion coefficient for La2S3.

Thermal expansion properties of organic crystals: a CSD study

The thermal expansion properties of crystalline organic compounds are investigated by data mining of the Cambridge Structural Database (CSD). The mean volumetric thermal expansion coefficient is 168.8 10-6K-1 and...

Магнитообъемные эффекты в сильно коррелированных фазах плутония

Thermodynamic spin fluctuations in strongly correlated plutonium (Pu) phases with exchange and spin–orbit interactions are considered. In α- and δ-Pu phases, the spin fluctuations lead to a negative magnetovolume effect that is determined by the parameter of intermode coupling and depends on features of the electron structure. It is shown that the negative volumetric thermal expansion coefficient of δ-Pu is related to an anomalously strong interaction of spin fluctuation modes.

First-principles investigation of mechanical and thermodynamic properties of nickel silicides at finite temperature -=SUP=-*-=/SUP=-

First-principles calculations are performed to investigate lattice parameters, elastic constants and 3D directional Young’s modulus E of nickel silicides (i.e., β-Ni_3Si, δ-Ni_2Si, θ-Ni_2Si, ε-NiSi, and θ-Ni_2Si), and thermodynamic properties, such as the Debye temperature, heat capacity, volumetric thermal expansion coefficient, at finite temperature are also explored in combination with the quasi-harmonic Debye model. The calculated results are in a good agreement with available experimental and theoretical values. The five compounds demonstrate elastic anisotropy. The dependence on the direction of stiffness is the greatest for δ-Ni_2Si and θ-Ni_2Si, when the stress is applied, while that for β-Ni_3Si is minimal. The bulk modulus B reduces with increasing temperature, implying that the resistance to volume deformation will weaken with temperature, and the capacity gradually descend for the compound sequence of β-Ni_3Si > δ-Ni_2Si > θ-Ni_2Si > ε-NiSi > θ-Ni_2Si. The temperature dependence of the Debye temperature ΘD is related to the change of lattice parameters, and ΘD gradually decreases for the compound sequence of ε-NiSi > β-Ni_3Si > δ-Ni_2Si > θ-Ni_2Si > θ-Ni_2Si. The volumetric thermal expansion coefficient αV, isochoric heat capacity and isobaric heat capacity C _ p of nickel silicides are proportional to T ^3 at low temperature, subsequently, αV and C _ p show modest linear change at high temperature, whereas C _v obeys the Dulong-Petit limit. In addition, β-Ni_3Si has the largest capability to store or release heat at high temperature. From the perspective of solid state physics, the thermodynamic properties at finite temperature can be used to guide further experimental works and design of novel nickel–silicon alloys.